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DIALOG Flle32: METADEX - 66-B2/Jun (Copr. Am. Soc Metals) (Item 4 of 12) User239t3 23Jun82
(O
00
Comroun(ties.
Bolte
MILLS. "Effects of
N.W. GHELBERG and E.
724758 8O-72O283
Management and Control of Heavy Metals In the Environment.
London. England. Sept. 1979
Pp 664, 8 x 113/4 In., Illustrated
Publ: Commission of the European
Postale IOO3, Luxembourg, 1979
Language: ENGLISH
Document Type- BOOK
Contents Include: I. BREMNER and C.F.
Diet on tha Toxlclty of Heavy Metala";
BODQR. "Arsenic Levels In the Environment and In Human Body In
a Copper Metallurgy Plant Area"; M. ABDULLA, S. SVENSSON and
A. NORDEN. "Antagonistic Effect of Zinc In Heavy Metal
Poisoning"; W.H. STRAIN. A.M. VARNES andO.A. HILL. JR.,
"Heavy Metal Contamination of Household Water"; B.2. OIAMANT,
"Environmental Health Impact of Heavy Metals In Wastewater
Sludge Applied to Cropland"; I. SAITO, "Removal of Chromium
(VI) In Aqueous Solutions by Activated Carbons"; K.K. CHIN and
J.H. TAV. "Laboratory Scale Treatment of Nickel-Bear Ing
Industrial Effluent"; C.p C. POON, "Removal of Copper. Nickel.
Zinc. Cadmium and Cyanide From Plating Wastewater by
Electroflotatlon"; N.L. GALE and B.C. WIXSON, "Control of
Heavy Metals In Lead Industry Effluents by Algae and Other
Aquatic Vegetation"; J. HRSAK and M. FUQAS. "Distribution of
Part leu I ate Lead. Zinc and Cadmium Around a Lead Smelter"; K.
SCHWITZGEBEL, R.V. COLLINS and R.T. COLEMAN. "Arsenic
Discharge 'From a Primary Copper Smelter"-; C.L. CHAPPELL and
S.L. WILLETTS. "Isolation of Heavy Metals From the
Environment"; A.N. CLARKE and O.U. WILSON, "The Removal of
Metallo-Cyanlde Complexes by Foam Flotation"; H J. JEBENS.
G.J. MEVERHOFER and D.J. MASTERS. "Removal of Heavy Metals
From Industrial Wastewaters"; F. EL-GOHARY. M.R. LASHEEN and
H I. ABDEL-SHAFV, "Trace Metal Removal From Wastewater Via
Chemical Treatment".
Descriptors: Toxicology; Water pollution; Pollution
abatement
Section Heading: 72 .(SPECIAL PUBLICATIONS) Journal
Announcement: BOOB
U.S. standards. Free oxygen and ozone produced at the anode
oxidized Nl In solution to form nickel oxides which
precipitated out. Hypochlorlte and C1 gas oxidized cyanide and
liberated heavy metals from the cyanide — metal complexes which
preceded alkaline precipitation. Performance equatIons .were
developed which Indicated the relative significance of the
effect of each operating variable on treatment performance and
suggested how the process could be better modified to trea.t
plating wastewaters of different character 1stIcs.--AA
Descriptors: Electroplating: Flotation; Pollution abatement:
Copper, Recovering; Nickel. Recovering: Zinc. Recovering;
Cadmium. Recovering
Section Heading: 58 .(METALLIC COATING) Journal
Announcement: BOOB
724528 8O-58O6I2
Removal of Copper, Nickel, Zinc, Cadmium and Cyanide From
Plating Wastewater by Electroflotatlon.
Poon, C P C
Management and Control of Heavy Metals In the Environment,
London. England. Sept. 1979
572-575
Pub)- Commission of the European Communities. Bolte
Postale IOO3, Luxembourg. 1979
Language. ENGLISH
Document Type: BOOK
The use of an electrof lotat Ion process to remove heavy
metals from plating wastewaters was Investigated. Cathodlc
generation of hydroxides raised the pH and reduced the metal
solubility, resulting In metal precipitation which was carried
up to the surface by the rising gas bubbles. Copper. Nl, In
and Cd were successfully removed, with the effluents meeting
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DIALOG File32: METAOEX - 66-82/Jun (Copr. Am Soc. Metals) (Item 6 of 12) User23913 23JunS2
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715594 8O-72OIB9
IronmakIng Conference. Vol. 35.
St. Louis. Mo.. 28-31 Mar. 1976
Pp 651. 81/4 x 111/2 In.. Illustrated (retroactive coverage)
Publ: Iron and Steel Society AIME. 345 E. 47th St., New
York. N.V. 1OO17. 1976
Language: ENGLISH
Document Type: BOOK
Contents Include: M. HATANO and M. FUKUDA. "The Effect on
the Blast Furnace Operation"; D.G. WHITE. "An Adaptive Model
Top-Gas Analysis";" O. KONCHAR and R.L. PRIOOY. Iron'; A.
MERTOOGAN and R. LANGHOFF. "Response Time of Composition of
Molten Iron to the Changes In Coke Moisture and Chemical
Composition of Sinter In the Blast Furnace"; T. OCHIAI. H
HOSHIIOE. "Vibration Forming Troughs"; R. SANTELLA. Furnace
Linings"; J.L. PUGH. "Anhydrous Clay Vs. Water-Base VOUNT.
JR., "Anhydrous Taphole Mixes for the Blast Furnace'; "Blast
Furnace Anhydrous Taphole Mixes'; R.E. ROSS, "Blast Taphole
Mixes"; J.A. WILLIAMS and O.A. HOMBERG. "Coke DesulfurIzatIon
and Sulfur Recovery Utilizing the Sulflran Process"; LOWNIE.
JR.. and A.o. HOFFMAN, "A Research Approach to Problems":; O.
GLASSMAN. "LISS CYAM System—an Improved and Cyanide Removal
From Coke-Plant Wastewater': J.G. MANDA. and D F CAIRNS,
"Development of One-Spot Enclosed Coke Pushing N.A. HASENACK,
R.B. VOGEL and F. HOMMINGA, "The and Their Behavior In the
Blast Furnace"; R.F. CNARE and G.M. Recoup System--a New
Method of Heat Recuperation In the Grate-Klin R.P. SOU2A.
"The Production of Pellets In CVRD Using Hydrated Is Growing
Up Fast": W.J. PRIESTNER. "Air Preheater System Stoves"; G.
VICARO and P.M. WECHSELBLATT, "High Furnaces"; E.L. GUNTHER
and H. SCHOPPA. "Panel In the Blast Furnace. Experience With
Stave Coolers on a Blast Hoesch Huttenwerke, AG"; H.U.
BLACKBURN. "Experience With Cooling at the Steel Co. of
Canada's No 4 Blast Furnace"; T.E. "Cooling Hazards In High
Tonnage Carbon Hearths"; C.M. on Blast-Furnace Tuyeres"; M.
YOSHINAGA. M. SANADA and "Industrialization of Briquet Blent
Coking Process": L.G. THOMPSON. "Selection of Coals and Coal
Mixes to Avoid Excessive Pressure"; E.J. OSTROWSKI. "Coal
Quality — Its Effect on the 0. FISCHLEY, "Some Aspects of
Blast Furnace Operation at Poor Quality Coking Coals In the
Coke Plant Mix"; P. SCHROTH ROBINSON. "The Effects of Alkali
Attack on Various Carbon LAMBERT. "Operation of Geneva Works
Blast Furnaces With Burdens"; F. FORES, J. BALLANO. J.
LAVANOERA. M. "Alkalles--Problem or Solution? at Altos Hornos
de VIzcaya SA"; and W.R. CORZILL1US. "Blast Furnace
Operations at Granite High Alkali Bearing Burdens"
R.T.Roberts., "MIOREX Yesterday H.A. KULBERG, "Current Status
of the FIOR de Venezuela Plant G.G.W. THOM and K. WILSON. "New
SL/RN Direct Reduction Mine"; J. CELADA and G.E. McCOMBS,
"HYL Direct LEONARD and S. MACOONALD. "Direct Reduction With
Gas Coal Gasification Process"; R.d. HELFINSTINE. "Charging
a Pilot Coke Oven"; D.A. COOPER, P.J. DE KOKER. I. and A N.
VENTER, "South African Experiences With Preheated Coal J.P.
GRAHAM. "Coal Preheat Ing--Research and Development In the
Kingdom": R.F. DAVIS. JR., "The COALTEK System--PIpelIne
Ovens": W L McHENRY. R.L LAND and A. FERNANDEX, and
Stait-Up of United States Steel's No. 2 Coke Battery at Gary
PRIES and F WACKERBARTH, "Experience Gained During the
Start-Up of the 7.5 Meter Coke Ovens In Fos-sur-Mer, France";
W.C. and J.L. BAYER. "Measurement and Evaluation of Heat
Distribution Ovens"; M. HIGUCHI. M. IIZUKA and Y. TAKASAKI,
"On Operational Control of No, 5 Sinter Machine at Fukuyama
Works, Nippon KK"; P.T. SEATON and F.8. TRAICE. "Development
of a Prediction of Sinter Plant Productivity From Ore
Properties"; H. J. OTTO, "Possibilities of Improvements to
Existing Sinter WILSON and G.K. JEFFERSON, "Operating
Experience of No. Gary Works"; S.E. NANNE. "Operating
Experience on Algoma's No. Furnace"; S. SH1MADA. "Production
of 13.5 Million Tons on Furnace".
Descriptors: Ironmaking; Blast furnaces; Heat recovery
Section Heading: 72 .(SPECIAL PUBLICATIONS) Journal
Announcement: BOOS
714467 8O-42O433
USS CYAM System--an Improved Process for Ammonia and Cyanide
Removal From Coke-Plant Wasteuater. (Retroactive Coverage).
Classman, D
Ironmaking Conference. Vol. 35, St. Louis. Mo.. 28-31
Mar. 1976
121-131
Publ: Iron and Steel Society AIME. 345 E. 47th St . New
York. N.Y. IOO17. 1976
Language: ENGLISH
Document Type: BOOK
Environmental regulatory agencies require the treatment of
coke-plant wastewater for removal of ammonia. cyanide and
phenol before discharge to streams and other utilities, uses
lime and avoids fouling. Wh&n used In conjunction with an
activated-sludge system, 'It provides an Ideal feed that
promotes smooth operation because of the virtual absence of
simple cyanides. These benefits are achieved with capital
costs that are competitive with for conventional free- and
fixed-ammonia stills.--AA
Descriptors: Coking: Water, pollution; Waste disposal;
Purification; Ammonia
Section Heading: 42 .(EXTRACTION AND SMELTING) Journal
Announcement: BOOB
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DIALOG FIIe32 METADEX - 66-B2/dun (Copr. Am. Soc. Metals) (Item B of 12) User23913 23JunB2
K)
00
U)
68OOBO 79-72O34O
Advanced Pollution Control for the Metal Finishing Industry.
Klsslmmee. Fla.. 5-7 Feb 1979
Pp 151. 81/2 x 11 In.. Illustrated
Publ. U.S. Environmental Protection Agency, Cincinnati,
Ohio 4S268, May 1979
Language: ENGLISH
Document Type: BOOK
Contents Include: M.E. BROWNING. J. KRALJIC and G.S.
Finishing Sludge Disposal; Economic. Legislative and Technical
for 1979"; C. ROY, "Methods and Technologies for Reducing the
Electroplating Sludges"; P.S. MINOR and R.J. BATSTONE,
Federal Republic of Germany's Centralized Waste Treatment
Approach In United States1; F.A. STEWARD and H.H. HEINZ,
"Economical Shop Case History"; d.A. BIENER, "City of Grand
Rapids, Industrial Waste Control"; A.F. LISANTI and S.O.
Proper Unit Processes for the Treatment of Electroplating
Wastewaters"; PRICE andC. NOVOTNY, "Water Recycling and
Nickel Recovery Exchange"; K.d. McNULTY and J.W. KUBAREWICZ,
"Field Closed-Loop Recovery of Zinc Cyanide Rlnsewater Using
Reverse Osmosis Evaporation"; d.L. EISENMANN. "Membrane
Processes for Metal Electroplating Rinse Water"; M.C. SCOTT.
"An EPA Heavy Metals Removal by Sulflde Precipitation"; C.P.
HUANG and "The Development of an Activated Carbon Process for
the Treatment of Chromium (VI)-Containing Plating Wastewater";
d. SANTO, et "Removal of Heavy Metals From Battery
Manufacturing Wastewaters by Cross-Flow Microf11tratIon";
G.D. McKEE, "Status of Analytical Cyanide"; V.S. KATARI, R.W.
GERSTLE and C.H. Degreaser Emissions*.
Descriptors: Pollution abatement; Electroplating
Section Heading: 72 .(SPECIAL PUBLICATIONS) dournal
Announcement: 7911
67986B 79-580679
Selecting the Proper Unit Processes for the Treatment of
Electroplating Wastewaters.
Llsantl. A F ; Megantz, S O
Advanced Pollution Control for the Metal Finishing Industry.
Ktsslmmee. Fla., 5-7 Feb. 1979
64-75
Publ: U.S. Environmental Protection Agency, Cincinnati,
Ohio 45268, May 1979
Language. ENGLISH
Document Type: BOOK
An engineering approach to the selection of unit processes
for the treatment of electroplating Wastewaters Is presented.
The approach consists of rinse water conservation, waste
stream segregation. stream characterization. field
treatablllty studies, laboratory treatablllty studies, system
design, construction and startup. Three electroplating
facilities are described to show differences In these systems
and how to accomodate unique problems with these systems Data
are given on removal of complexed Cu, Nl other metals,
electrolytic reduction of segregated Cr(+6), treatment of
cyanide. effect of polishing- filtration, effect of total
treatment. analysis of effluent, projected concentrations In
chemical O demand waste, removal of soluble and Insoluble oil,
quality of combined treated Wastewaters. destruction of
amenable cyanide, filter press performance and ultraf11tratton
effluent quality of permeate soluble oil.--H.A D.
Descriptors: Electroplating; Water pollution; Pollution
abatement; Effluents; Recovering
Section Heading: 58 .(METALLIC COATING) dournal
Announcement: 7911
67986O 79-58O671
Environmental Pollution Control Alternatives: Economics of
Wastewater Treatment Alternatives for the Electroplating
Industry. (Pamphlet).
Pp 72
Publ: Industrial Environmental Research Laboratory,
Cincinnati, Ohio 45268. dune 1979
Report Number: EPA 625/S-79-O16
Language: ENGLISH
Document Type: REPORT
This report provides a detailed examination of the costs
associated with various water pollution control alternatives
available to the metal finishing Industry. The document also
provides some figures for computing the savings associated
with various good housekeeping practices such as spent bath
reuse and minimization of water usage. The document Is geared
to the plater who may be evaluating control costs for the
first time. However. even those experienced In these matters
will probably benefit from the discussions of housekeeping
practices, various recovery techniques and emerging
technologies.--AA
Descriptors: Electroplating; Cyanides; Recycling; Effluents;
Water pollution; Pollution abatement
Section Heading: 58 .(METALLIC COATING) .Journal
Announcement: 7911
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DIALOG File32. METADEX - 66-82/Jun (Copr. Am. Soc. Metals) (Item II of 12) User239l3 23JunB2
6522O3 79-72OO11
Proceedings of the 31st Industrial Waste Conference.
Bel I, d M
Lafayette. Ind., 6-8 May 1976
Pp 1164. 6 x 91/4 In.. Illustrated
Publ: Ann Arbor Science Publishers. Inc.. P.O. Box 1425.
Ann Arbor. Mich. 481O6.. 1976
Language. ENGLISH
Document Type BOOK
Contents Include: J. McVAUGH and W.T. WALL, Jr.. Metals
Wastewater Treatment Effluent Quality Vs. Sludge Treatment";
METRV and M.E. HARRIS. "A New Concept for Treating Leachate
Runoff Waters From a Taconlte Transshipment Facility"; M-H.
Wu. and C-P. HUANG. "Regeneration of Activated Carbon for the
Chromium"; W.E. LINK and J.G. RABOSKY, "Fluoride Ion
Waste-Water Employing Calcium Precipitation and Iron Salt
WARNKE. K.G. THOMAS and S.C. CREASON. "Reclaiming Reverse
Osmosis"; J.A. DRAGO and J.R. BUCHHOLZ. "Removal Contaminants
From Aqueous Laboratory Wastes by Chemical Treatment";
PROBER, P.B. MELNYK and L.A. MANSFIELD. "Treatment Furnace
Effluents to Inhibit Formation of Iron-Cyanide Complexes";
HOCKENBURY. J.M BOWER and A.W. LOVEN, "Metal Wastewater
Treatment' a Case History".
Descriptors: Waste disposal; Pollution abatement
Section Heading: 72 .(SPECIAL PUBLICATIONS) Journal
Announcement: 79O1
CD
•t^ 652171 79-71OO4O
Industrial Wastewater Ozonatlon.
Hardlsty. D M : Rosen. H M
Proceedings of the 32nd Industrial Waste Conference.
Lafayette. Ind.. 1O-12 May 1977
294-3O2
Publ: Ann Arbor Science Publishers, Inc.. Ann Arbor. Mich
1978
Language ENGLISH
Document Type: BOOK
Ozone generation and application Is an established
technology with numerous applications In Industrial Wastewater
treatment. The key advantage offered by ozone Is Its strong
oxidizing capability and Its clean, add-nothing feature. As
for any Wastewater treatment system. the cost factors require
careful assessment The economics of using O feed vs. air feed
bear on this cost analysis. Treatment of effluents with
materials such as cyanide, phenol, color and COD Is
feasible.1O refs.--AA
Descriptors: Wastes, Oxidation; Ozone: Pollution abatement
Sect ion Heading: 71 .(GENERAL AND NONCLASSIFIED) Journal
Announcement 79O1
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DIALOG F I le.12
METADEX - 66 82/Jun (Copr. Am. Soc. Metals) (Item I of 9) User239l3 23jun82
3162
t-J
co
Cn
75599O 8I-57OO54
Uastewater and Hazardous Solid Waste Disposal In the
Aluminum Products Industry.
Marino, M
Met Finish. .Oct. 198O. 78. (tO). 2t-27. 4O
Language: ENGLISH
Document Type: ARTICLE
Government regulations concerning the disposal of solid and
liquid wastes in the Al industry are discussed. The existing
regulations for waste water discharge were established by the
Federal Water Pollution Control Act Amendments of 1972. The
practical application of these regulations to At product
plants (anodizing, chromating and phosphatlng) is described
and the impact of probable future regulatory changes is
'outlined. Solid waste disposal is regulated by the 1976
Resource Conservation and Recovery Act. The proposed EPA
guidelines for defining hazardous solid wastes are Included.
Recommendations for meeting guidelines and treatment cost
minimization are Included.--G.P.K.
Descriptors: Aluminum base alloys. Coating; Waste disposal;
Pollution abatement; Anodizing; Chromating
Section Heading: 57 (FINISHING) Journal Announcement: 81O2
724758 8O-72O283
Management and Control of Heavy Metals In the Environment.
London. England. Sept. 1979
Pp 66-1. 8 x 113/4 In., Illustrated
Pub): Commission of the European Communities.
Postale 1OO3. Luxembourg, 1979
Language- ENGLISH
Document Type: BOOK
Contents Include: I. BREMNER and C.F.
Diet on the Toxlclty of Heavy Metals";
BODOR, "Arsenic Levels In the Environment and in Human Body in
a Copper Metallurgy Plant Area"; «. ABOULLA. S. SVENSSON and
A. NORDEN, "Antagonistic Effect of Zinc in Heavy Metal
Poisoning"; W.H. STRAIN. A.W. VARNES and 0. A. HILL. JR..
"Heavy Metal Contamination of Household Water"; B.Z. DIAMANT,
"Environmental Health Impact of Heavy Metals In Wastewater
Sludge Applied to Cropland"; I. SAITO, "Removal of Chromium
(VI) In Aqueous Solutions by Activated Carbons"; K.K. CHIN and
J.H. TAV. "Laboratory Scale Treatment of Nickel-Bear Ing
Industrial Effluent"; C.P.C. POON, "Removal of Copper, Nickel,
Zinc, Cadmium and Cyanide From Plating Wastewater by
Electrof lotat ion"; N.L GALE andB.G. WIXSON, "Control of
Heavy Metals In Lead Industry Effluents by Algae and Other
Aquatic Vegetation"; J. HRSAK and M. FUGAS, "Distribution of
Partlculate Lead, Zinc and Cadmium Around a Lead Smelter"; K
SCHWITZGEBEL, R.V. COLLINS and R.T. COLEMAN, "Arsenic
Discharge From a Primary Copper Smelter"; C.L. CHAPPEtL and
S.L. WILLETTS, "Isolation of Heavy Metals From the
Environment"; A.N. CLARKE and D.J. WILSON. "The Removal of
Metallo-Cyanlde Complexes by Foam Flotation"; H.J. JE8ENS,
G.J. MEVERHOFER and D.J MASTERS. "Removal of Heavy Metals
From Industrial Wasteualets", F. EL-GOHARY. M R. LASHEEN and
Bolte
MILLS. "Effects of
N.W. GHEL8ERG and E.
H.I. ABDEL-SHAFV,
Chemical Treatment".
Descriptors: Toxicology;
abatement
Section Heading: 72 .(SPFCIAL PUBLICATIONS)
Announcement: BOOS
Trace Metal Removal From Wastewater Via
Water pollutIon; Pol Hit Ion
Journal
68OO8O 79-72O340
Advanced Pollution Control for the Metal Finishing Industry.
Klsslromee, Fla., 5-7 Feb. 1979
Pp 151. et/2 x It in.. Illustrated
Publ: U.S. Environmental Protection Agency. Cincinnati,
Ohio 45268. May 1979
Language: ENGLISH
Document Type: BOOK
Contents Include: M.E. BROWNING. J. KRALJIC and G.S.
Finishing Sludge Disposal; Economic. Legislative and Technical
for 1979"; C. ROY, "Methods and Technologies for Reducing the
Electroplating Sludges"; P.S. MINOR and R.J. BATSTONE,
Federal Republic of Germany's Centralized Waste Treatment
Approach In United States"; F.A. STEWARD and H.H. HEINZ.
"Economical Shop Case History"; J.A. BIENER, "City of Grand
Rapids. Industrial Waste Control"; A.F. LISANTI and S.O.
Proper Unit Processes for the Treatment of Electroplating
Wastewaters"; PRICE and C. NOVOTNY. "Water Recycling and
Nickel Recovery Exchange*; K.J McNULTY and J.w. KUBAREW1CZ.
"Field Closed-Loop Recovery of Zinc Cyanide Rlnsewater Using
Reverse Osmosis Evaporation"; J.L. EISENMANN. "Membrane
Processes for Metal Electroplating Rinse Water"; M.C. SCOTT.
"An EPA Heavy Metals Removal by Sulflde Precipitation"; C.P.
HUANG and "The Development of an Activated Carbon Process for
the Treatment of Chromium (VI)-Contalnlng Plating Wastewater";
J. SANTO. et "Removal of Heavy Metals From Battery
Manufacturing Wastewaters by Cross-Flow Mlcrof11tratIon" :
G.O. McKEE, "Status of Analytical Cyanide"; V.S. KATARI. R.W.
GERSTLE and C.H. Oegreaser Emissions".
Descriptors: Pollution abatement; Electroplating
Section Heading: 72 .(SPECIAL PUBLICATIONS) Journal
Announcement: 7911
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DIALOG Flle32: METADEX - 66-82/Jun (Copr. Am. Soc Metals) (Item 4 of 9) User 23913 23jur)B2
679872 79-58O6B3
The Development of an Activated Carbon Process for the
Treatment of Chromium (VI(--Containing Plating Wasteuater.
Huang, C P ; Bowers, A R
Advanced Pollution Control for the Metal Finishing Industry,
Kisstmmee, Ma.. 5-7 Feb. 1979
114-122
Publ: U.S. Environmental Protection Agency, Cincinnati,
Ohio 45268. May 1979
Language: ENGLISH
Document Type: BOOK
The recent developments tn the use of activated C for total
Cr removal from plating wastewaters are discussed. The topics
Include Interactions of (VI) with activated C In batch
experiments and packed columns, operation of packed columns,
regeneration of exhausted activated C by thermal, caustic,
combined thermal-caustic and acid methods, and the removal of
Cr (III!. are given for the effects of C bed size, depth.
increasing Cr concentration, number of regeneration cycles and
effect of time and caustic concentration on desorptIon.2O
refs --H.A 0.
Descriptors: Chromium, Recovering; Electroplating; Water
pollution; Activated carbon, Reactions (chemical); Effluents;
Regenerators
Section Heading: 58 .(METALLIC COATING) Journal
Announcement: 7911
Descriptors: Waste disposal; Pollution abatement
Section Heading: 72 .(SPECIAL PUBLICATIONS)
Announcement: 79O6
668O68 79-58O326
Treatment of Zinc Plating and Oil Bearing Washer Wasteuater.
Kreye. W C ; Olver. J W ; Sutton, H C ; V/orch. f R
The 33rd Industrial Waste Conference, Lafayette, Ind .
9-It May 1978
155-164
Publ: Ann Arbor Science Publishers Inc., P.O Box i425.
Ann Arbor. Mich. 481O6. 1979
Language: ENGLISH
Document Type: BOOK
The treatment of Zn and Cr plating and washer wastewaters of
a major manufacturer Is described. Following a survey of the
wastewaters, laboratory testing, treatment system evaluation,
an interim treatment system and pilot testing, a final
treatment system was built. Details and data are given for the
system.--H.A.O.
Descriptors: Zinc plating; Chromium plating; Wastes; Water
pollution; Pollution abatement
Section Heading: 58 .(METALLIC COATING) Journal
Announcement: 79O6
to
00
01
668318 79-72O17O
The 33rd Industrial Waste Conference.
Lafayette. Ind., 9-11 May 1978
Pp IO28. 6x9 In.. Illustrated
Publ: Ann Arbor Science Publishers Inc. P.O. Box 1425. Ann
Arbor. Mich 481O6. 1979
Language. ENGLISH
Document Type: BOOK
The Conference Is under the direction of the Purdue
University Civil Engineering and the Dlv. of Conferences and
Continuation Services, cooperation with the Indiana State
Board of Health. Indiana Stream Control Board. Indiana
Environmental Management Board, Indiana Dept. Natural
Resources. Indiana Section of tha American Water Works Assoc.,
Water Pollution Control Assoc. and Indiana Section of the
American Civil Engineers. Contents Include: M.E. McGUIRE.
D R. FAUSCH. "Pollution Control Through Water Conservation at
a Gray Foundry"; W.C. KREVE, J.W. OLVER. H.C. SUTTON and
Zinc Plating and Oil Bearing Washer Wastewater"; E.O.
"Ammonia Steam Stripping at Miscellaneous Nonferrous Metals
Plants, Histories"; W.M. WINN and E.L MORGAN, "Stream
Ecosystem Municipal Sewage Discharges and Accommodation to
Aluminum Industry Effluents"; W R. KNOCKE, T. CLEVENGER, M.M.
GHOSH of Metals From Electroplating Wastes"; I L. LEE and
R.E. of Oily Machinery Wastes"; D.M. SOBOROFF. J.D. TROVER
One-Step Method for Recycling Waste Chromic Ac Id--SulfurIc
Acid Solutions"; M.C. FISCHER, "Wet Scrubber Water Treatment
in the Steel Industry Using Lamella Gravity Settlers"; J
"Extended Aeration of Coke-Plant Effluents"
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DIALOG Flle32: METADEX - 66-82/Jun (Copr. Am. Soc. Metals) (Item 7 of
9) User23913 23jun82
K)
CO
6522O3 79-72OO1I
Proceedings of the 31st Industrial Waste Conference.
Bell. J M
Lafayette, Ind.. 6-8 May 1976
Pp 1164. 6 x 91/4 In.. Illustrated
Publ: Ann Arbor Science Publishers. Inc., P.O. Box 1425,
Ann Arbor, Mich. 481O6.. 1976
Language: ENGLISH
Document Type: BOOK
Contents Include: J. McVAUGH and W.T. WALL. Jr.. Metals
Wastewater Treatment Effluent Quality Vs. Sludge Treatment";
METRY and M.E. HARRIS. "A New Concept for Treating Leachate
Runoff Waters From a Taconlte Transshipment Facility"; M-H.
Wu. and C-P. HUANG. "Regeneration of Activated Carbon for the
Chromium"; W.E LINK and J.G. RABOSKY. "Fluoride Ion
Waste-Water Employing Calcium Precipitation and Iron Salt
WARNKE, K.G. THOMAS and S.C. CREASON. "Reclaiming Reverse
Osmosis"; J.A. DRAGO and J.R. BUCHHOLZ, "Removal Contaminants
From Aqueous Laboratory Wastes by Chemical Treatment";
PROBER. P.B. MELNYK and L.A MANSFIELD. "Treatment Furnace
Effluents to Inhibit Formation of Iron-Cyanide Complexes";
HOCKENBURY. J.M. BOWER and A.W. LOVEN, "Metal Wastewater
Treatment: a Case History".
Descriptors: Waste disposal; Pollution abatement
Section Heading: 72 .(SPECIAL PUBLICATIONS) Journal
Announcement1 79O1
652172 79-71OO41
Sulfex--a New Process Technology for Removal of Heavy Metals
From Waste Streams.
Scott, M C
Proceedings of the 32nd Industrial Waste Conference.
Lafayette. Ind., 1O-12 May 1977
622-629
Publ: Ann Arbor Science Publishers. Inc.. Ann Arbor, Mich.
1978
Language: ENGLISH
Document Type: BOOK
The Sulfex process described represents an economical and
feasible approach to sulflde precipitation of heavy metals. As
such It offers the advantages of more complete removal of
metals from waste streams than hydroxide precipitation.
generally at pH ranges which are acceptable discharge. It
removes most chelated metals from wastewaters and reduces
hexavalent -Cr as It precipitates the other heavy metals as
sulfldes. It Is a new process which has been successfully
piloted on three waste --AA
Descriptors: Sludge; Precipitation; Sulfldes; Wastes;
Chromium; Iron
Section Heading- 71 (GENERAL AND NONCLASSIFIEO) Journal
Announcement' 79O1
Chromium.
Wu, M-H ; Hsu. D Y ; Huang. C-P
Proceedings of the 31st Industrial Waste Conference.
Lafayette. Ind.. 6-8 May 1976
409-419
Publ: Ann Arbor Science Publishers. Inc., Ann Arbor. Mich.
1976
Language: ENGLISH
Document Type: BOOK
Recent studies have shown that Cr can be effectively removed
by the C adsorption process, but the practical application of
this technique to the treatment of Industrial uastewater
depends not only upon the adsorption capacity but also on the
feasibility of regenerating the spent C. Research was
conducted to study some physical and chemical techniques for
the regeneration of Cr-loaded activated C. The activated C,
Calgon flltrasorb effectively removed hexavelent Cr The
removal efficiency Is governed by pH and the ratio of Cr to C
Among the three regeneration techniques studied--caustIc
desorptlon, thermal activation and a combined caustIc-thermaI
process — the latter gave the best regeneration results.
showing that > 97% of the original removal efficiency was
maintained through three regeneration cycles. To achieve high
adsorption and regeneration efficiencies. It Is recommended
that a relatively low Initial Cr loading (e.g. O CIS g
Cr(VI)/g C) be applied for the adsorption cycle and that the
used C be regenerated at a level of surface occupancy (e.g.
O.O5O g Cr(VI)/g C) well below the max. adsorption capacity. II
refs.--AA
Descriptors: Chromium, Sorptlon; Industrial wastes;
Activated carbon, Sorptlon; Adsorption; Reclamation
Section Heading: 71 .(GENERAL AND NONCLASSIFIEO) Journal
Announcement: 79O1
652152 79-7IOO2I
Regeneration of Activated Carbon for the Adsorption of
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DIALOG Flle4l: Politic-" Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 1 of 98) User239l3 23Jun82
00
en
or DDT In Factory Effluent by Thin-Layer
J.V.
Jawaharlal Nehru Univ.. New Delhi. India
4. NO. 516, pp. 391-395, Publ.Yr:
ENGLISH
82 O2169
Characterization
Chroma t ography
Sharma. S.K.; Dave
Sell. Environ. Scl.
ENVIRON. INT VOL.
I98O
SUMMARY LANGUAGE -
Languages: ENGLISH
Thin- layer chromatography (TLC) Is shown as an effective,
inexpensive, reliable, and less time-consuming technique for
simple and effective monitoring of persistent toxicant- 1 Ike
present In Its manufacturing plant effluent Aqueous untreated
and treated grab and compost effluent samples were collected.
extracted with a solvent and concentrated and chroma tographed
both for qualitative and quantitative analysis for p.p'-DOT
and related compounds. This technique was sucessful and can
form an effective. Inexpensive method to be used by the
developing countries, which have limited financial resources.
Descriptors: chromatography; DDT; effluents; monitoring;
toxicants; pollutant detection; wastewater treatment; cost
benefit analysis
82-O2O9O
Economical and Efficient Phosphorus Control at a
Domestic-Industrial Wastewater Plant
Van Dam. O.
Address Not Stated
J WATER POLLUT. CONTR. FED VOL. 53, NO. 12. pp.
1732-1737. Publ.Yr- 1981
SUMMARY LANGUAGE - ENGLISH
Languages ENGLISH
It Is the purpose of this paper to discuss the special
challenges the merged waste flow posed to design and
subsequent operation of the treatment plant. How concentrated
side streams. such as heat treatment supernatants, must be
considered In overall plant efficiency Is discussed. The
techniques used to control phosphorus at a very low cost are
presented. A summary of several years of plant efficiency and
cost figures accompany the text. The Grand Haven, Mich.,
wastewater plant was designed to best accomodate the domestic
wastewater from Grand Haven and the adjacent village of Spring
Lake, as well as a sizable contribution of wastes from a local
chrome and vegetable tanning operation. Five-year operating
results and cost experience of phosphorus control with the
addition of waste pickle liquor to primary settling tank
Influent followed by activated sludge treatment Is shown.
Descriptors: wastewater treatment plants; economics;
phosphorus; activated sludge process: technology; cost benefit
analysis; chromium; settling basins
Plants
Lue-Hlng. C. ; Lord I, D.T.; Kelada, N.P.
Metro. Sanitary Dlst. Greater Chicago, IL
AlChE Nat. Mtg. Boston, Portland, Chicago I960
IN "WATER - 198O VOL. 77. NO. 2O9. pp 144-ISO,
Publ.Yr: 1981
AICHE. 345 EAST 47 ST.. NEW YORK. NY 1OOI7
SUMMARY LANGUAGE - ENGLISH
Languages: ENGLISH
The U.S. Environmental Protection Agency has Issued a list
of 129 priority pollutants which Include metals. cyanides,
phenols, pesticides and other organlcs. The Metropolitan
Sanitary District of Greater Chicago (MSDGC) which operates
seven treatment plants has regulated heavy metals, phenols and
cyanides for a number of years The heavy metals found In the
Influents Include chromium, copper, zinc. Iron, nickel, and
cadmium. Substantial but variable removals do occur with the
effluents reaching some background level for a specific metal.
These metals are found to concentrate In the treatment plant
sludges. The results of a screening of the occurrence of the
priority organlcs at four of the MSDGC treatment plants showed
relatively few organlcs occurring In detectable quantities.
The concentrations of those found were highly variable but
generally less than 1OO mu g/l In the Influents and less than
2O mu g/1 In the effuents.
Descriptors: pollutants; organic compounds; heavy metals;
effluents; wastewater treatment plants; sludge; cyanides;
phenol; pesticides: contamination
82-O2O74
Fate of Priority Pollutants In Large Municipal Treatment
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NJ
CO
82-O2O13
Water Purification System
Shorn, J.
Sys. Eng.
U.S.
p. 2O34.
Publ.Yr:
& Mfg. Corp.. Stoughton. MA
PAT. OFF. GAZ.
VOL. 10O7, NO. 5,
1981
Pat. No. 1,276, t76
Languages . ENGL I SH
A method of purifying water including. combining at least
17OO ppra of a combining agent with wastewater at a pH of fnom
7.1 to 14 with the molar ratio of satd combining agent to the
impurities In satd wastewater being 1:1 on greater so that a
part tele-water blend Is formed wherein said impur 1 1 les are
bound with said combining agent In particles of size at least
1O angstroms; said combining agent Including inorganic metal
hydro* tde with the metal be Ing selected from the group
consisting essentially of Iron aluminum. tin. copper, zinc,
cadmium nickel . cobal t , s 1 1 icon, bar I urn,
and chrome.
Descr tptors : Pur if 1 cat Ion; Wastewater treatment ;
sizes; Inorganic compounds; pH; Patent;
management ; Particle size
calcium, manganese.
Part Id e
Heavy metals; Water
82-00578
Industrial Waste-Water Reuse by Selective Silica Removal
Matson, J.V.
Houston, TX
U.S. PAT OFF. GAZ VOL. 1OO7. NO. 5, p 2O35. Publ.Yr:
1981
Pat. No. 4.276. 18O
Languages: ENGLISH
A method for maintaining silica content In a rectrculating
cooling water system containing waten conditioning chemicals
selected from the group consisting of sulfates. phosphonates
and chromates below a level at which silica scale formation
occurs without discharging blowdown from the system with
consequentlal el in(mat ion from the system of satd water
cond111on 1ng chem1ca1s on resu111ng po11utIon of the
environment, which include continuously diverting a portion of
the chemically conditioned cooling water from said cooling
system as a side stream.
Descr iptors. Cool ing systems; Industrlal effluents;
Wastewater treatment; Water reuse; Chemicals; Environmental
protec tIon. ActIvated alumina; Patent
At Elmo-Calf tannery a new system for recovering chromium
has been installed. Ear 1ler some process 1tquors were
reclrculated back to the process. But the amount of chromium
In the waste waten was too high. The new system was worked out
through laboratory tests and tests in pilot plant. During the
tests magnesium oxide together with anionic polymers were
used. The fulI scale plant was then constructed for
precipitation with either magnesium oxide or sodium carbonate.
The plant which has been in operation with sodium carbonate as
precipitation agent since 1978 with good results. consists of
batchwise precipitation and settlIng of the wastewater and
thIcken tng and dewa ten t ng and dIsso1vIng the siudge. As
dissolving agent concentrated sulfunlc acid has been used. The
chromium liquor Is then reclrculated to the tanning processes.
DescrIptors: Tanning Industry wastes; Chromium; Sludge
dewaterIng; Polymers; RecyclIng; Wastewater treatment
Identifiers: Elmo Calf tannery
81-O7214
Two Step Removal of Metal Ions From Effluents
Cassella. V.J.; Irani, M.R.
PO Corp., Valley Forge. PA
U.S. PAT. OFF. GAZ VOL. 1OO4. NO. 3.
1981
Pat. No. 4.256,577
Languages: ENGLISH
A process f on reducing the metal
aqueous effluents to less than O.I part
consisting of the sequential steps of: a. Agitating an aqueous
effluent containing up to 150O ppm of a metal Ion selected
from the group cons 1st ing of diva lent manganese, copper .
cadmium, lead. Iron, cobal t . nickel and z tnc and tn ivalent
chromium and Iron; b. Adding an aqueous solut Ion of an
tnonganlc base to adjust the pH of the effluent to a value
between 7.O and 9.O.
Descn iptons : Heavy metal s ; Ef f luents; Ions; Wastewater
treatment; pH; Patent
1131.
Publ.Yr*
on concentration of
per ml 11 Ion (ppm)
82-OO563
RenIng av Kromhattlgt Avloppsvatten och Ateranvandnlng av
Utfallt Krom Vld Elmo-Calf AB, Svenljunga
Emanuelsson. I.; Persson, C E ; Horrdln, S
Scandlaconsult AB. Goteborg
VATTEN VOL. 36. NO. 4, pp. 343-351. Publ.Yr 198O
Languages- ENGLISH
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to
^
O
B1-O7183
New Method of Regeneration of An*on Exchangers Used for
Recovering Chromates From Wastewater
Paw 1owsk \ . L. ; K1epacka. B.; 2aIewskI. R.
Oept. Chem. Tech., Inst. Chem., tubI In, Poland
WATER RES VOL 15. NO. 1O, pp. 1153-1*56, Publ.Yr:
1981
Languages• ENGLISH
A new economically attractive method of recovery of water
and chromates from wastewater has been presented. In order to
obtain a high enough concentrated regeneration effuent for
refilling plating bath, high concentrated sodium hydroxide
(45%) was used for regeneration of a weakly based anlon
exchanger bed (Wofat It AO 41). Further Increase of the
concentration of the regeneration effluent was obtained by
recyclIng certain frontal and tat 1 parts of regeneration
effuent to raw wastewater. It permits to recycle only a high
concentrated part of the regeneration effluent to refilling
the platfng bath. The Influence of flow rates, doses of sodium
hydroxide and reclrculatIon ratio on the average concentration
of the regeneration effluent and Ion exchange capacity has
been presented.
Descr Iptors: Ef fluents; Resource management; Wastewater
treatment; Recycling; Flow rates; Chromates; Sodium compounds;
Anton exchangers
81-O7175
Elimination of Toxic Metals From Wastewater by an Integrated
Wastewater Treatment/Water Reclamation
Smith, R.; Wtechers, S.G.
Council Scl. A Indust. Res.
Inst. Water Res.
2. pp. 65-7O.
Publ.Yr:
. Rep.
1981
S.
Nat.
Afr .
WATER SA VOL. 7, NO.
Languages: ENGLISH
The overal 1 effect tveness of a pi tot -scale. Integrated
wastewater treatment/water reclamation plant for the removal
of the eight toxic metals listed In the U.S. Environmental
Protect Ion Agency Nat tonal Inter Im Pr Imary Or Ink Ing Water
Regu 1 a t 1 ons < ar sen I c . bar I um , cadm I urn , chrom 1 urn . 1 ead ,
mercury, selenium and silver) was Investigated. Certain unit
processes In the system were shown to be capable of acting as
additional safety barriers against toxic metal contamination.
The most s Igntf leant processes for toxic metal removal were
dent tr If (cat Ion. chemical mix Ing/clar If teat Ion and act I ve
carbon treatment .
Descr I p tors : Wastewater treatment ; EPA ; Federal regulat Ions;
Toxic metals; Contaminants; Activated carbon
1981
Languages: ENGLISH
The wastewaters from paint stripping and surface treatment
operations on aircraft contain a range of materials Including
phenolIc compounds and chromium. The wastewaters are generated
errat leally and only during part of the paint stripping.
repainting cycle. A Fenton's reagent system employing 10O-2OO
rag.L super(-) super(l) of ferrous Iron and hydrogen peroxide
at a weight ratio of hydrogen peroxide to phenol of 2.5-3.O to
1, has been shown to oxidise phenols and reduce any he>
chromium to trIvalent chromium. Subsequent 1 Ime tr
removed the organic residues, chromium and phosphate
s1udge and produced a supernatant su1table for dIsch
sewers and subsequent biological treatment. The lab
results have been confirmed by pilot plant scale studte
DescrIptors: Wastewater; Phenol compounds; Chromium;
valent
atment
to the
rge to
ratory
Laboratory methods;
trea tment; AIrcraf t
Contain t nant s; Paint strl pp 1 ng; Sur f ace
81-O7129
Mechan t caI Aera 11on Versus
Stabilization Pond Treatment
Iwugo, K.O,
Publ. Health Eng. . Univ. Lagos.
EFFLUENT AND WATER TREAT. J VOL
Publ.Vr: 1981
Languages: ENGLISH
This article presents the
Investigations on the treatment of
Hydrogen Perox1de
21, NO.
results of
molasses-based
pp. 8-18.
laboratory
yeast and
chrome-based tannery wastewaters In waste stabilization ponds.
DescrIptors: Tannery Industry wastes; Wastewater; Ponds;
Laboratory methods; Water treatment
81-O7159
Treatment of Paint-Stripping Wastewaters Which Contain
Phenol and Chromium
Barnes, 0.; O'Hara, M.; Samuel, E ; Waters. D.
Sch. Civil Eng , Unlv NSW. Kensington, Austral
ENVIRON TECH. LETT VOL. 2, NO 2. pp. 85-94. Publ . Vr •
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DIALOG F1te4t: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs ) (Item 12 of 9B) User23913 23jvjn82
KJ
VO
H
chrome from waste water
hexava lent va 1 ence state.
81-O7O18
Chrome Removal Waste Treatment Process
Cassldy, J.D. ; Stelnbrecher . L.
Amchein Prod., Inc., Ambler, PA
U.S. PAT. OFF. GAZ VOL. 1O05 . NO. 1. p. 256. Publ.Yr.
1981
Pat. No. 4.26O.491
Languages: ENGLISH
In a process for the removal of
wh 1 ch * nc 1 udes chrom 1 urn i n the
wherein the pH of said waste water fa adjusted to below about
5, wherein a reducing agent Is added to said waste water while
Its pH Is below about 5 In an amount sufficient to convert all
of the chromium present In the hexava lent valence state to the
tr 1 valent valence state.
Descr Iptors : Wastewater treatment ; pH; Chromium; Pol lut Ion
control ; Patent
81-O5676
Main Compounds Behavior In Kraft Wastes Cleaning by Acid
Coagulation and Carbon Adsorption
Aguado . J . ; Rodr 1 guez , J . U . ; T 1 J ero . J .
Dept , Qulmlca Indust . , Fac. C lend as
Complu tense, Madr Id, Spain
J. ENVIRON. SCI . HEALTH VOL. A16, NO.
Publ . Vr : 1981
Languages: ENGLISH
A kraf t wastewater cleaning method, cons 1st Ing In acid
coagulation and carbon adsorption 1s studied on a chemical
basis. The results obtained show that acid coagulation mainly
produces a precipitation as well as a partial acldolysls of
1 Ignln compounds; a certain retention of celluloslc compounds
was also noticed. Subsequent carbon adsorption substantlaly
removes carbohydrates and pract leal ly a! I of the remaining
1 Ignln Ic compounds.
Descr Iptors : Paper Industry wastes; Preclpl tat 1 on; Carbon;
Adsorpt Ion; Wastewater treatment; Spectroscopy ; Chroma tography
Qu 1m leas , Unlv .
4, pp. 4O5-418.
said munitions In trace amounts as low as 25 parts per billion
onto a reverse phase, high performance liquid chromatographtc
column; (b) chromatographlcally separating said munitions on
said column by elution with a mobile phase comprising methanol
and water; and, (c) monitoring the absorbance of the resulting
eluant In the ultra-violet region to provide a quantitative
determination of the munitions present In said sample.
PescrIptors: Wastewater treatment; LIquld chromatography;
AbsorptIon; Water samplIng; Pur 1fleatIon; Chemicals; Patent
8I-O5578
Elimination of Toxic Metals From Wastewater by an Integrated
Wastewater Treatment/Water Reclamation System
Smith, R.; Wlechers, S.G.
Nat. Inst. Water Res. Councl1 Scl. Indust. Res., Pretoria,
Rep. S. Afrlea
WATER SA VOL. 7, NO 2. pp. 65-7O, Publ.Yr: 1981
Languages: ENGLISH
The overal1 effectIveness of a pilot-scale. Integrated
wastewater treatment/water reclamatIon plant for the removal
of the eight toxic metals 1tsted In the U.S. Environmental
Protect Ion Agency Natlonal Inter 1m PrImary DrInk Ing Water
ReguIat Ions (arsenIc barlum, cadm1urn, chrom1um, 1ead,
mercury, selenium and silver) was Investigated. Certain unit
processes In the system were shown to be capable of acting as
additional safety barriers against toxic metal contamination.
The most signIf leant processes for toxIc metal remova1 were
denttrIfIcatlon. chemical mlxlng/clarIftcation and active
carbon treatment.
DescrIptors: Wastewater treatment; Potable waters; Heavy
metals; ContamlnatIon; Act Ivated carbon; EPA; Federal
regulat tons; Water reuse
81-O56OO
Quantification of the Munitions, HMX. RDX, and TNT In Waste
Water by Liquid Chromatography
Cattran, D.E.; Stanford, T.B ; Graffeo, A.P.
Dept. Secretary Army. Wash., DC
U.S. PAT OFF. GAZ VOL. IOO3, NO. 4, p. 1557, Publ.Yr:
1981
Pat. No 4.252,537
Languages: ENGLISH
A method for the quantitative detection of alIphatIc
nltroamlne and nltroaromatIc munitions selected from the group
consist Ing of 1.3,5,7-tetrant tro-1,3,5,7-tetraazacyclooctane,
1,3,5~trlnltro~ 1.3.5-trlazacycIohexane, 2,4.6-trInltrotoluene.
comblnatIons thereof, and the degradatIon products thereof. In
liquid samples. which Includes (a) directly Injecting up to
40O mlcrollters of a non-concentrated liquid sample containing
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DIALOG FUe41' Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 16 of 98) User23913 23Jun82
81-O5574
Activated Sludge and Activated Carbon Treatment of a Wood
Preserving Effluent Containing Pentachlorophenol
Quo, P.H.H.; Fowlle. P.J.A.; Cairns, V W.; Jank. B.E.
Wastewater Tech. Ctr.. Environ. Protect. Serv.. Environ.
Can.
Publ.Yr• 19BO
ENVIRONMENTAL PROTECTION SERVICE. ENVIRONMENT CAN.. OTTAWA,
ONT. K1A 1C8, CAN.
ISBN. O-662-1O978-3; Rept. No. EPS 4-WP-8O-2
Languages: ENGLISH
A sIx-month monltoning and wastewater treatment plant
effluent upgrading-program was carried out at AbitIbl-Northern
Wood Preservers Limited. Thunder Bay, Ontario, a plant which
preserves wood with creosote, pentachlorophenol (PCP) and
chromated copper arsenate (CCA). Treatment of the wastewater,
after oil separatIon and flow equalIzatIon by the extended
aeration activated sludge process. gave good removal of most
organ1cs; however, PCP remova1 averaged only 35% and the
ef fluent was toxic to rainbow trout. Treatment of the
activated sludge effluent by carbon adsorption resulted In
effectIve PCP removal and nan-toxic effluents. ActIvated
carbon treatment of wastewater, after oil separation and flow
equalization, gave good removals of organ!cs and PCP.
DescrIptors: Wastewater treatment plant; Effluent; AeratIon;
Activated sludge process; Toxic materials; Contaminants; PCP
compounds
8I-O5377
Heavy Metals In the Ruhr River and Their Budget In the
Catchment Area
Imhoff, K.R.; Koppe, P.; Oietz. F.
Ruhrverband. FRG
lOth Int. Conf Int. Assoc. Water Pollut. Res. (IAWPR)
Toronto. Ont. dun. 23-27, 198O
WATER SCI. & TECH VOL. 13. NO. I. Publ.Yr: 1981
Languages: ENGLISH
Numerous analyses of heavy metals have been evaluated with
respect to origin. concentration, behavior and fate of these
elements In the 4.488 km super(2) large catchment area of the
most Intens1vely used Ruhr RIver. For the ratio of the
dissolved and the total heavy metal concentration In Ruhr
water the foltowing topological progress Ion wlth IncreasIng
dissolved fractIon results: tead< copper< z1nc< nickel<
chrom1um< cadmium. A heavy metal balance has demonstrated that
55% of the heavy metals In the Ruhr River are discharged from
municipal and Industrial waste water treatment plants. 45% are
of geochemlcal orIgln. The municipal treatment plants receive
31% of the heavy metals from domestic and 69% from industrial
waste water. These fIgures represent the average of all
analysed heavy metals. The fraction of the particular elements
varies considerably. For example 9O% of the chromium, 65% of
nickel and cadmium and 5O% of copper and zinc are discharged
by industries. The "population equivalent" of heavy metals was
caleulated from the results of 19 plants receIvlng only
domestic waste water deducting the fraction contained In the
drink Ing water.
DescrIptors: Heavy metals; Rivers; Industr1a1
Wastewater treatment plants; Potable water
Ident Iflers: Ruhr River
effluents;
81-O4O11
Control of pollution In Waters Containing Heavy Metals
Klncannon. D.F.; Bates, M.H.; DeVrles. R.N.
DK St. Univ., Stlllwater, Sch Civil Eng
Publ.Yr. 198O
NTIS. SPRINGFIELD. VA
PB81-124133
Languages: ENGLISH
An integrated set of experiments wre carried out on the fate
of chromium and copper In biological waste water treatment
processes. aqueous environments, and soII systems. A rotatIng
biological contactor and activated sludge were used as the
waste water treatment processes; Still water. Oklahoma area
lake and river water and sediments. as the aqueous
environments; and sandy and red sllty clay soils. as the soil
systems. While It was determined that chromium was removed by
the lake and river sediments but not generally removed by
biological treatment processes or by algae, it was found that
copper was removed by all systems. Removal efficiencies of the
metals were highly dependent upon operating and environmental
conditions. Sediments and soils had strong affinities for
copper, and uptake could be correlated with soil type.
DescrIptors: Wastewater treatment; Act Iva ted sludge process;
Soils: Freshwater environments; Algae; Heavy metals
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DIALOG FI1e41: Pollution Abstracts - 7O-B2/Apr (Copr Cambridge Sci Abs) (Item 19 of 98) User239l3 23junB2
VOL. 13. NO. 2
Publ.Yr: 1981
K)
va
U)
81-O398I
Type A Zeolite In the Activated Sludge Process-II: Heavy
Metal Removal
Carrondo, M.J.T.; Lester. J.N.; Perry. R.
Publ. Health Eng. Lab., Imperial Col).. London. G.B.
d. WATER POLLUT. CONTR. FED. VOL. 53. NO. 3 , pp.
344-351 , Publ.Yr: 1981
Languages: ENGLISH
Pilot plant studies were conducted over a range of type A
zeolite concentrations expected In settled wastewater and at
two degrees of calcium exchange for sodium In the zeolite. Two
hydraulic regimes also were examined. An Identical pilot
plant. operating under conditions Identical to those of the
test unit and to which no zeolite was added. provided a
control. At the high calcium exchange rate, no effect was
detected on heavy metal removal. At the low calcium exchange,
the removals of cadmium, chromium, nickel, and lead were
unaffected. There also seemed to be a slight deterioration In
zinc removal and an equally small Improvement In copper
removal, but the evidence for both was Inconclusive The
general order of decreasing removal observed was Cu > Cr. Zn,
Pb > Cd > N1. Although not studied so Intensively, the removal
of Iron seemed to be unaffected by zeolite.
Descriptors: Activated sludge process; Wastewater treatment;
Heavy metals; Water pollutants; Chemical compounds
Identifiers, zeolite
81-O3936
Activated Carbon Processes for the Treatment of Chromium
(VI(-Containing Industrial Wastewaters
Bowers. A.R.; Huang, C.P.
Environ. Eng. Prog., Dept. Civil Eng., Univ. DE, Newark
loth Int. Conf. Int. Assoc Water Poltut. Res. (IAWPR)
Toronto, Ont. dun. 23-27. 198O
WATER SCI. ft TECH. VOL. 13, NO. I . Publ.Yr: 1981
Languages: ENGLISH
Various operational systems using activated carbon for the
removal of Chromium (VI) from synthetic wasteuaters have been
examined In the laboratory. The Influence of controllable
parameters, such as pH. Cr(VI) concentration. column depth.
and mixing In solution were evaluated for the possibility of
scale-up to an economically feasible treatment system.
Completely-mixed. column, and rotating carbon disk systems
were compared as system design alternatives.
Descriptors: Activated carbon; Wastewater treatment;
Chromium; Heavy metals; Economics; Engineering; Water
pur IfleatIon
WATER SCI. & TECH.
Languages- ENGLISH
Percolation of secondary effluent from oxidation ponds to
the groundwater aquifer, which was studied In a large-scale
field operation, acted as an efficient advanced wastewater
treatment system. The major processes Involved were: slow sand
filtration, biological degradation, nitrification.
denl tr If Icat Ion, chemical precipitation, adsorption and Ion
exchange. Excellent removal was obtained by effluent passage
through the soil -aquifer system for several Important
pollutants. Including: phosphorus, partlculate organic matter,
collform bacteria, cadmium and chromium. Good removal was also
obtained for soluble organlcs (expressed as DOC or filtered
KMnO sub(4) consumption).
Descriptors: Effluent treatment; Oxidation; Groundwa ters ;
Aquifers; Filtration; Blodegradat Ion; Denl trlf Icat Ion;
Nitrification; Adsorption: Ion exchange; Wastewater treatment
81-O3O9O
Hexachlorocyclopentadlene Contamination of a Municipal
Wasteuater Treatment Plant
Komlnsky. JR.: Wtsseman, C.L.; Morse, D.L.
Nat. Inst. Occup. Safety Health, Cincinnati. Oh.
AM. INDUST. HYG. ASSOC. d. VOL. 41. NO. 8 . pp 552-556
Publ.Yr: Aug. 19BO
Languages: ENGLISH
In Mar. 1977 hexachlotocyclopentadlene (HCCPD) and
octachlorocyclopentene (OCCP) entered the Morris Forman
Wastewater Treatment plant In Louisville. Kentucky. Airborne
HCCPD concentrations of a blue haze generated by cleanup
procedures measured 19.2OO ppb. A NIOSH questionnaire sought
Information on type and duration of symptoms. HCCPD and OCCP
were collected on pre-extracted Chromosorb 1O2 (2O/4O mesh)
packed Into a 7 cm long 4 mm ID glass tube and then analyzed
using a gas chromatograph equipped with a flame lonlzatlon
detector. The type of protective equipment used varied with
the conditions of exposure. Usable responses to medical
questionnaires were received from 177 treatment plant
employees.
Descriptors: TOXICOLOGY AND HEALTH
Identifiers: hexachlorocyc1opentadIne contamination of
wastewater treatment plants
81-O3878
Treatment Effects and Pollution Dangers of Secondary
Effluent Percolation to Groundwater
Idelovltch, f. : Mlchall, M.
Sewage Reclam Dept , Tel Aviv. Israel
Tenth Int Conf. IAWPR Toronto, Ont. dun 23-27. 198O
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DIALOG F11e4): Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sd Abs) (Item 23 of 98) User23913 23Jun82
K)
B1-O2773
Trace Organic Behavior In Soli Columns During Rapid
Infiltration of Secondary Wasteuater
Bouwer, E.J.; McCarty, P.L,; Lance, J.C.
Env iron. Eng, Scl . , Civil Eng. Dept., Stanford. CA
WATER RES. VOt. 15, NO. 1 . pp. 151-159 . Publ.Yr;
1981
Languages: ENGLISH
Secondary treated municipal wastewater from the City of
Phoenix was applled to three laboratory-scale sol 1 columns at
var lous Inf11trat ion rates typical of high-rate land
application systems. and a fourth column was Inundated with
tapwater to serve as a control. Samples of the column Influent
and effluent streams, collected with continuous flow-through
systems to prevent organic volat11IzatIon losses, were
ana ^yzed for organic compounds us 1ng gas chromatography/mass
spectrometer. This study was performed to give a general
IndlcatIon of the behavior of trace organleg In sol I column
systems with an attempt to Indicate the presence of various
removaI processes.
Descriptors: SEWAGE & WASTEWATER TREATMENT; LAND POLLUTION
Identifiers: trace organic behavior In soil columns during
Infiltration of wastewater
81-O2772
Efficiencies of Liquid-Liquid Extraction and XAD-4 and XAD-7
Resfns In Collecting Organic Compounds From a Coke Plant's
Effluent
Schaeffer, Q. J. ; TIgwelI, O.C.; Somant, S.M.; Janardan, K.G.
IL E.P.A. Springfield, IL
BULL. ENVIRON, CONTAM. TOXICOL. VOL. 25. NO. 4 , pp,
569-573 , 'Publ.Yr: Oct. I98O
Languages: ENGLISH
The authors have examined the theoretleal requirements of
composite sampling, the propagation of errors which occur from
samp)ing through tdentIf teat ion, and the eff iclency of
sampling methods using capture-recapture methods. Estimates of
the total number of compounds which might be Identifiable by
gas chroma tograhpy-mass spec trometry, have been made. The
theoretical findings have been translated Into practice by the
development of a multichannel sampler (Tigwell and Schaeffer
198Q) which permits the simultaneous collection of a sample by
up to four methods. The present paper will describe how these
elements Interptayed in a study of a coke plant's waste water.
Descriptors: SEWAGE 8 WASTEWATER TREATMENT
Identifiers: organic compounds extraction from coke plant
effluents
Languages: ENGLISH
Oecationized wastewater Is directed onto weakly base ion
exchanger bed Amber lite IRA 67. The cation exchanger bed is
regenerated by means of 5% H sub(2)SO sub(4). The anfon
exchanger bed Is regenerated with \Q>% NaOH. Some fractions of
the front and tall
Into raw wastevtat
regeneration efflue
that rectrculatIon
regeneration efflue
f the regeneratIon effluent are recycled
r to Increase the concentration of the
t. Using computer analysis it was shown
f about 23% of chromates contained (n the
t Into raw wastewater Increases twice the
concentration of the recovered concentrate of chromates from
about 25g to 47g Cr svjper(+6)/dm super(3).
Descriptors: SEWAGE * WASTEWATER TREATMENT
Identifiers: ion exchange In recycling of plating effluents
81-O27O3
Influence of Sludge Age on Heavy Metal Removal In the
Activated Sludge Process
Sterrltt, R.M.; Lester. J.N.
Publ. Health Eng. Lab . Imperial Coll., London. Engl.
WATER RES. VOL. 15. NO. 1 . pp. 59-65 , Publ.Vr: 1981
Languages. ENGLISH
In a laboratory simulation of the activated sludge process
ten heavy metals were added continuously to the system which
was allowed to equilibrate at six sludge ages between 3 and
16d. Cobalt, manganese and molybdenum removals were poor and
were unaffected by changes In the sludge age The highest
removal efficiencies for the other metals occurred at the I5d
sludge age. Chromium (trlvalent) and cadmium had the highest
removal efficiencies, typically greater than 5Q'J4. The
behaviour of the majority of the metals which were removed to
a significant extent was related to one of the parameters
influenced by sludge age. The metals which were poorly removed
showed little affinity for the activated sludge.
Descriptors: SEWAGE & WASTEWATER TREATMENT
Identifiers: sludge age Influence on heavy metal removal
BI-02759
Ion Exchange In the Recycling of Plating Effluents
Paw I owsk I, L . ; 2a I ewsk 1 . R .
Inst. Chern. Inst, Math Marie Curie-Sklodowsda Univ
EFFLUENT AND WATER TREAT J VOL. 2O. NO. 12
581-58b , Publ Yr. Dec 198O
PP
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DIALOG Filell. Pollution Abstracts - 7O-82/Api (Copr. Cambridge Set Abs) (Item 27 of 98) User23913 23juriB2
81-02692
Comparison of the Characteristics of Soluble Organic
Nitrogen In Untreated and Activated Sludge Treated Wastewaters
Parkin. G.f ; McCarty. P.L.
Pept. Civil Eng.. Drexel Univ., Phlla.. PA
WATER RES. VOL. 15. NO. I , pp. 139-149 . Publ.Vr:
1981
Languages: ENGLISH
Soluble organic materials containing nitrogen (SON) are
present In effluents from activated sludge treatment of
domestic wastewater. but little Is known about the sources and
characteristics of these materials. The characteristics of SON
In untreated wastewaters and activated sludge effluents were
evaluated. Characterization techniques used Included low
mtcroblal seed blodegradabl11 ty . molecular weight distribution
using gel filtration chromatography. removal by activated
carbon and Ion exchange, and analysis for free and combined
am(no acids.
Descriptors: SEWAGE & WASTEWATER TREATMENT
Identifiers: organic nitrogen In untreated and treated
sludge treated wastewater
81-O26BO
Field Disposal of Methyl Parathlon Using Acidified Powdered
Zinc
Butler. L C.; Stalff. D.C.; Davis. J.E.; Sovocool. G.W.
Wenatchee Pesticides Res. Br.. Health Effects Res. Lab.,
U.S. EPA, Wenatchee, Wa.
J. ENVIRON. SCI. HEALTH VOL. BI6, NO. 1 , pp. 49-58 .
Publ Yr: 1981
Languages- ENGLISH
The degradation of methyl parathlon In soil with various
amounts of acidified powdered zinc under field conditions was
studied. Treatment was progressively more effective with
Increasing amounts of zinc Disappearance of parent compound
was followed for 2 1/2 years. The expected conversion product
aminomethyl parathlon and Its N-methyl derivative were formed.
Amlnomethyl parathlon was shown to be Identical to an
authentic standard The other specific positional Isomers were
considered likely, but were not proven by mass spectrometry.
Structure elucidation was made with high resolution mass
spectrometry. using the direct Insertion probe, and with gas
chrotnatography/low resolution mass spectrometry.
Descriptors SEWAGE & WASTEWATER TREATMENT
Identifiers field disposal of methyl parathlon
Illus. 9O refs.
Abs. (Available from NTIS. Springfield, VA 22161)
Languages: ENGLISH
TREATMENT CODES: D .(DESCRIPTIVE) ; I .(INVESTIGATIVE/OBSER-
VATION)
A floe foam flotation pilot plant removed Pb and Zn In
dilute aqueous solution to quite low concentrations. Design
Improvements are presented. The floe foam flotation of Zn Is
readily carried out with aluminum hydroxide (AI(OH)3) and
sodium lauryl sulfate (NLS). Chromium hydroxide Is floated
with NLS, but adsorbing colloid flotation of Cr+3 with ferric
hydroxide (Fe(OH)3) or AI(OH)3 yielded better results. Cobalt
and Nl levels are reduced to =1 mg/L by flotation with A1(OH)3
and NLS. The Mnt2 levels can be reduced to 1-2 mg/L by
flotation with Fe(OH)3 and NLS. Floe foam flotation of Cu was
compatible with several precipitation pretreatments (soda ash.
lime. Fe(OH)3, and A1(OH)3). although modifications were
needed to prevent Interference from excessive Ca or CO3-2.
Therefore, floe foam flotation can be used as a polishing
treatment. The flotation of mixtures of Cut2, Pbt2, and Zn+2
was conducted using Fe(OH)3 and NLS. The flotation of simple
and complexed cyanides and mixtures of metal cyanide complexes
was also conducted with Fe(OH)3 and NLS; a pH of =5 Is
optimum. A surface adsorption model for floe foam flotation
was analyzed and accounted for the effects of surfactant
concentration, lontc strength, specifically adsorbed Ions, and
surfactant hydrocarbon chain length. (AM)
Descriptors: Flotation; Industrial wastes; Wastewater
treatment; Pilot plants; Engineering; FlocculatIon; Ions;
Surfactants; Iron compounds; Aluminum compounds: Heavy metals;
Zinc; Nickel; Manganese; Chromium; Cobalt; Copper; Lead;
Chemical treatment; Adsorption
Identifiers: floe foam flotation
Industrial uastewaters:
8I-O1797
Foam flotation treatment of
Laboratory and pi lot scale.
Wilson, D J ; Thackston. E. L.
Vanderbllt Univ., Nashville. TN 37235
II.S Environmental Protection Agency. Office of Research and
Development Environmental Protection Technology Series
CorJfin FPTSBT Publ Vr Jun I98O
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DIALOG Flle4t: Pollution Abstracts - 7O-82/Apr (Copr, Cambridge Scl Abs) (Item 3O of 98) User23913 23Jun82
3174
10
B1-O1795
Sulflde precipitation of heavy metals.
Rob i nson, A. K., Sum, J. C.
Boeing Commercial Airplane Co., Manufacturing Research and
Development. P O. Box 3707, Seattle, WA 98124
U.S. Environmental Protection Agency. Office of Research and
Oeve1opment EnvIronmentaI Protect Ion Techno1ogy Ser1es
Coden: EPTSBT PubI Vr: Jun 198O
IIlus. 16 refs,
Abs. (Available from NTIS. Springfield. VA 22161)
Languages: ENGL!SK
TREATMENT CODES• I .(INVESTIGATIVE/OBSERVATION) ; 0
.(DESCRIPTIVE) ; E .(ECONOMIC/COMMERCIAL/MARKET)
The sulflde precipitation of heavy metals from Industrial
wastewaters was evaluated. Five processes were compared In
bench-scale, contInuous-flow equipment-convent tonal 1 Ime
processing, conventional lime processing plus filtration, lime
with a sulflde polishing and filtration, lime with sulflde.
and lime with sulflde plus filtration. Wastewater samples
from 14 metal work Ing Industrles were processed through the
bench-scale equipment using all 5 processes. Reductions In
the concentrations of Cd, Cr, Cu, N1, and Zn. plus selected
other metals, were measured by atomic absorption chemical
analysis. Capital and operating costs for the processes were
compared for 3 plant stzes-37 85 ro3/d (1O.OOO gpd). 757 m3/d
(2OO.OOO gpd). and 1.B93 m3/d (5OO.OOO gpd). To reduce the
levels of Cd. Cu, Ml. or Zn from a wastewater treatment plant
using conventional lime processing, the addition of a final
filtration should be considered first. If filtration does not
achieve the desired low levels, then a sulflde polIshlng
process with added filtration Is recommended. If reduction of
the levels of Cr, Pb, Ag, or Sn Is required, the conventional
lime process plus filtration 1s recommended. The sulflde
process did not s ignlficantly reduce the levels of these
metals. Details are Included on the use of a specific Ion
electrode for the control of sulflde additions. (AM)
DescrIptors• Heavy metals; Precipltat ion; Was tewater
treatment; Sulfur compounds; Industrlal effluents; L I me;
F11tratIon; Metal Industry wastes; Economics; Engineering;
Cadmium; Copper; Chromium; Nickel*, 2Inc; Chemical treatment
Ident 1flers: sulfIte precipI tat ion
Doc Type: JOURNAL PAPER CONFERENCE PAPER
TREATMENT CODES: T .(THEORETICAL/MATHEMATICAL) ; D
.(DESCRIPTIVE)
A model was developed to represent the 1IquId-phase
reduct Ion of Cr+6 by SO2, the s Imul tarieous compet 111 ve
reaction of DO with S02, and O2 reaeratlon. The model Is
applicable to both batch and continuous stirred tank reactors
and gives conservat1ve results compared to batch and
contInuous-flow data. Sulfur dioxide and Its salts reduce
Cr+6 to Cr+3. The reaction rate increases with Increasing
reactant concentratIon and temperature and decreasIng pH.
Residual Cr is lower In a batch reactor than 1n a continuous
reactor of equal residence time. DO competes with Cr+6 for
SO2. Oxygen-saturated cooling tower blowdown is the Initial
source of O2 to the reaction, and O2 enters the system by
reaeratlon as the DO concentration Is depleted. Reaeratlon
can be sIgnlfleant and Is a serlous enemy of chromate
reduction. (AM.FT)
DescrIptors: Mathematleal models; KInetIcs; Chromium; Heavy
metals; Cooling systems; Reduction; Sulfur compounds; Chemical
react Ions; Chemical treatment: Wastewater treatment; Sulfur
dloxIde; DO; AeratIon
Identifiers: cooling tower blowdown; Cr(VI); hexavalent Cr
81-01755
Kinetic model for chromate reduction In cooling tower
blowdown.
Kunz. R. G.; Hess, T. C.; Yen, A. F.; Arseneaux, A. A.
Air Products and Chemicals. Inc.. P.O. Box 538. Allentown,
PA 181O5
86th national meeting of the American Institute of Chemical
Engineers Houston. Texas Apr 1-5. 1979
Amerlean Institute of Chemical Engineers
Water Pol tut ion Control Federal Ion. Journal 52(9).
2327-2339, Coden: JWPFA5 Publ Yr- Sep 198O
1 Ilus. 29 refs.
Eng.. Fr , Ger., Port., Span abs.
Languages ENGLISH
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DIALOG Ftle41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc I Abs) (Item 32 of 98) User23913 23Jun82
-J
BI-O1723
Pretreatment of Industrial discharges to publicly owned
treatment works.
Ongerth. J. E.; OeWalle. F. B.
Brown and Calduell Engineers. 6OO First Ave.. Seattle, WA
9B1O4
Water Pollution Control Federation. Journal 52(8),
2246-2256. Coden: JWPFAS Pub'l . Yr: Aug 198O
11lus. no refs.
Eng.. Fr., Ger., Port., Span, abs.
Languages: ENGLISH
Ooc Type: JOURNAL PAPER CONFERENCE PAPER
TREATMENT CODES: I .(INVESTIGATIVE/OBSERVATION)
The effectiveness of an Industrial pretreatroent program to
limit the discharge of toxic metals and organIcs Into publicly
owned treatment works was evaluated. Measured median
Industrial discharge concentrations were as follows: O.69 mg/L
Zn; O.65 mg/L Cu; O.17 mg/L Pb; O.29 rog/L Cr; O.1O mg/L Nl;
and O.O2 mg/L Cd. Analysis of wastewater from different
treatment plants showed the presence of 36 priority
pollutants. All groups but phth.alates showed an Increase with
Increasing plant flow and percentage of Industrial
.contribution, Indicating that Industrial pretreatment can
reduce wastewater concentration levels by >l/2. Primary
treatment was effective In removing high molecular weight
compounds, and secondary treatment can remove volatile
compounds through air stripping and additional adsorption and
degradation by bacterial solids. (AM)
Descriptors: Industrial effluents: Wastewater treatment;
Heavy metals; Toxic materials; Pollution control; Zinc; Copper
; Lead; Chromium; Nickel; Cadmium
Identifiers- pretreatment
8I-OI7O9
ChromatographIc behavior of humlc materials extracted from
Barberton sludge.
Marios. G. P.; Tsal, E.
Univ. of Akron, 3O2 E. Buchtel Ave., Akron, OH 44325
Water. Air. and Soil Pollution; an International Journal of
Environmental Pollution 13(3). 373-377. Coden: WAPLAC
Publ.Yr Sep 198O
Illus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: I .(INVESTIGATIVE/OBSERVATION)
Humlc and fulvlc acids extracted from alkali treated
municipal sludge contain more higher molecular weight
materials than from secondary wastewater effluents. This
suggests that higher molecular weight materials (>3O.OOO) are
more easily entrapped on the protelnaceous surface of the
btomass. About 28% of the sludge COD Is humlc material. The
humtc acid fraction Is of a higher molecular weight than the
fulvlc acid fraction. The value of the E4-E6 ratio Indicates
that humlc materials of raw sludges are of recent origin.
While the higher molecular weight humlc materials (>3O.OOO)
would be easily adsorbed on the soil structure. the lower
molecular weight material may have a higher mobility In the
transport of heavy metals when the sludge Is applied to soils.
(AM.FT)
Descriptors: Acids; Alkalies; Sludges; Chrotnatography;
Bloraass; COD; Wastewater treatment; Sewage treatment; Organic
wastes; Effluents; Municipal wastewaters; Heavy metals
Identifiers: humlc acid; fulvlc acid; high molecular weight
materials
81-O17O3
Further studies on the Influence of zeolite type A on metal
transfer In the activated sludge process.
Perry, R.; Obeng, L. A.; Lester, J. N.
Univ. of London. Imperial College. Civil Eng. Dept.. Public
Health and Water Resource Eng. Section. London SW7 2BU.
E ngIand
Environment International 3(3). 225-23O, Coden: ENVIOW
Publ.Yr: 198O
11lus. refs.
Sum.
Languages: ENGLISH
Ooc Type: JOURNAL PAPER
TREATMENT CODES: I .(INVESTIGATIVE/OBSERVATION)
The effect of zeolite type A on metal (Cd, Cr, Cu. Nl. Pb.
Zn) removal by activated sludge was Investigated using
laboratory activated sludge simulations operated at constant
aerator sludge age and settler surface loading. Different
concentrations of raw zeolite and zeolite extracted from
washing powder (O, 15, 3O. 6O. I2O mg/L) were Introduced Into
the simulations. The zeolite was added at 2 degrees of Ca
exchanged for Na, 25% and 75% of the maximum exchange
capacity. Metals were added at concentrations typical of
mixed domestic-Industrial wastewaters. Apparently zeolite
does not adversely affect metal removal at the concentrations
and under the conditions used, but could slightly Improve
removal of Pb and, to a lesser extent, Zn and Cd. The
greatest .Improvement occurred on the Initial addition of
zeolite; however, the Improvement Is not as great as that
observed under conditions In the presence of detergent P04-3.
(MS.FT)
Descriptors: Heavy metals; Activated sludge process;
Simulation; Detergents; Lead; Zinc; Cadmium; Chromium; Copper:
Nickel: Surfactants; Sewage treatment; Wastewater treatment;
Pollutant removal; Phosphate removal
Identifiers: zeolite; metal removal; 6 heavy metals
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DIALOG F1le4t: Pollution Abstracts - 7O-82/Apr (Copr. -Cambridge Scl Abs) (Item 35 of 98) User 23913 23]un82
O
0
o
CHEEA3
8I-OI-IO9
Effluent rules are here for Inorganic chemicals.
Shaw. d. S.
World News, Washington, DC
Chemical Engineering 87(18), 53-55. Coden:
Pub I.Yr: Sep 8. I98O
11lus no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER '
EPA's new guidelines for Inorganic chemicals apply to
pollutants In the wastewaters of 152 out of 75O US Inorganic
chemical plants. but only IO7 will have to make changes to
conform. at an estimated cost of $41.2 million. Segments of
the Industry most seriously affected are titanium dioxide and
chromium pigment producers. The crux of the EPA effort Is the
determination of "best available technology'' (BAT), and the
requirement that this standard be Incorporated Into
Industrial-wastewater permits. Compliance with BAT Is
mandated by duly 1984. The guidelines are expressed
numerically, and any suitable technology can be used which
ensures compliance. The guidelines also propose slightly
revised "best practicable technology" (BPT) standards. EPA
also established somewhat more stringent standards than BAT
for firms which discharge Into municipal sewage treatment
plants and set standards for new plants. In most cases, BAT
translates Into BPT plus additional end-of-plpe treatment.
EPA Is still considering other options for the final rules and
Is seeking Information about the costs of complying with RCRA
to determine the effect these will have on the total cost of
meeting the various wastewater regulations. (FT)
Descriptors: EPA; Federal regulations;
wastes; Inorganic compounds; Wastewaters:
Chromium compounds; Pigments; Effluents
Identifiers: best available technology;
technology
Chemical Industry
Titanium compounds:
best practicable
Languages: ENGLISH
Doc Type: dOURNAL PAPER CONFERENCE PAPER
Rusting Is an oxidation process that converts fe from its
elemental state to Fe+2 or Fe+3. During oxidation. Fe has
potential for reducing substances fro
states, e.g., Cr+6. Thus. If the
passed through a stock of rusting tin
Sn and Fe to Sn+2 and Fe+2 oxidation
time, the Cr+6 Is reduced to Cr+3.
procedure over the standard method o
sizes of tin can and dlfferen
their higher oxidation
hromlc acid solution Is
ans It will oxidize the
tates, and at the same
he advantages of the
S03-2 or S02 reduction
wastewater feeding
characteristics to evaluate the effectiveness of the process.
The more heavily rusted tin cans are more effective In
reducing Cr+6. Generally. a retention time of 12 hr Is
required to reduce 9O/S of the Cr+6 to Cr+3, but for purposes
of design, a 24-hr retention time Is Ideal to reduce Cr+6
almost to negligible level. Calcium carbonate Is used as a
precipitating agent. The chemical cost of conventional Cr
treatment processes Is twice that of the new process using
rusted tin cans based on a IOO m3/d of combined wastewater
with 5 ppm SO2 and pH 3.O. (FT)
Descriptors: Waste reuse; Waste management: Materials
recovery; Tin; Chromium; Metal finishing industry wastes;
Waste treatment; Pollution control; Chemical oxidation;
Kinetics; Economics
Identifiers: rusted tin cans; Cr plating wastes
B1-OO759
Utilization of waste tin cans In the control of chromium
plating wastes.
Ouano. E. A. R ; Arellano, F.
Quezon City, Philippines
Second recycling world congress- New and better uses of
secondary.resources Manila, Philippines Mar 19-22, 1979
National Science Development Board of the Philippines-Asian
Recycling Association-Bureau International de la
Recuperation-United Kingdom Society of Chemical
Industry-United Kingdom "Conservation ft RecyclIng''-Unlted
Kingdom Institution of Metallurgists-Illinois Institute of
Technology-United States Research Institute-United Kingdom
Institution of Production Engineers-Clean Japan Center-dapan
Waste Management Association-United States Bureau of Mines
CONSERVATION & RECYCLING 3(3-4), 355-359. Coden:
CRECD2 Publ.Vr. 1979
iIlus. S refs
No abs.
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DIALOG Flle4t. Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 37 of 98) User239t3 23junB2
to
(.0
8 I-OO66S
Wastewater treatment plant works overtime.
Frltch. G. H.
Howard R. Green Co . Green Engineering Bldg., Cedar Rapids,
IA 52401
Water and Wastes Engineering 17(9). 7O-73. Coden:
WWAEA2 Publ.Yr: Sep I98O
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The Amana, Iowa, wastewater treatment plant, operated and
maintained by Amana Refrigeration, Inc. (which contributes
>SO% of the design loading). Is described. The plant's
Industrial wastes-containing a high concentration of heavy
metals-and Its domestic wastes are segregated, with the latter
transported through gravity collector sewers to a pumping
station where It Is ground before being sent to a flow
equalization tank. A concrete splitter box divides the flow
equally to 2 aeration basins. Aerobic digestion Is
accomplished using a center flow mounted mixing system;
treated effluent Is disinfected by chlorInatIon. The system
has a hydraulic capacity of 3OO.OOO gpd and an organic
capacity of 51O Ib of BOD5/d. The segregated waste streams
are pretreated separately. An unusual filtering system then
removes metal hydroxides without prior clarification'. The
waste streams are segregated Into 2 categor1es-Cr+6 wastes and
acid-alkali wastes. Hexavalent chromium Is reduced to Cr-t-3
with sodium bisulfite under acidic conditions, blended with
the acid-alkali waste, and neutralized to precipitate
Insoluble metal hydroxides. Ferrous sulfate agglomerates the
gelatinous waste. which Is filtered through PVC filter tubes.
(FT)
Descriptors Wastewater treatment plants; Industrial wastes;
Aerobic process; Iowa; Engineering; Biological treatment;
Heavy metals; Domestic wastes; Wastewater treatment
Identifiers: Middle Amana; Amana Refrigeration, Inc..
drain field, which In turn reduces the required size of the
field. The units are also designed to keep untreated sewage
from entering the drain field. (FT)
Descriptors: Aerobic process; Sewage treatment; Aerobic
systems; Domestic wastes
Identifiers: Pennsylvania State Univ.; CA-15 and CA-5
aerobic treatment units: Chromaglass Corp.
81-OO599
Electrolytic ferrlte formation system for heavy metal
removal.
Nojlrl, N. ; Tanaka. N. ; Sato. K.; Sakal, V.
Mitsubishi Petrochemical Co.. Ltd,. Central Research Lab..
Aml-cho, Ibarakl-ken. Japan
Water Pollution Control Federation. Journal 52(7).
1898-1906, Coden: JWPFA5 Publ.Yr: Jul 198O
Illus. 3 refs.
Eng.. Fr.. Oer., Port.. Span. abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
An electrolytic coagulation process was developed for
removal of heavy metals from Industrial wastewaters. The
process consists of the following processes: an electro-bath,
In which Cr+6 Is reduced to Cr+3; polymer coagulation and
settling; and formation of ferrlte In the settled sludge.
Ferrlte sludge Is separated In a magnetic separator. The Cr
In ferrlte sludge Is not soluble In water. Phosphate and
silicon dioxide also are Incorporated Into the ferrlte sludge.
Supernatant water from the settling contains very little Cr.
(AM)
Descriptors: Electrochemistry; Heavy metals; Materials
recovery; Contaminant removal; Wastewater treatment; Ions;
Engineering; Mathematical analysis: Industrial effluents;
Separation processes; Chromium
Identifiers: electrolytic ferrlte formation
ASSOCIATION OF PENNSYLVANIA.
Publ.Yr: Jul-Aug 198O
81-00615
Aerobic sewage treatment system performance tested at Penn
State.
Anonymous
WATER POLLUTION CONTROL
MAGAZINE 13(4), 16-18.
1 Ilus. no refs.
No abs.
Languages: ENGLISH
Doc Type- JOURNAL PAPER
Two aerobic treatment units. CA-5 and CA-15. manufactured by
the Cromaglass Corporation have undergone 6 mo of tests at the
Pennsylvania State University Wastewater Treatment Plant and
have been approved by the Pennsylvania Department of
Environmental Resources. The CA-5 Is a 5OO-gpd model suitable
for single family dwellings that can remove 82/4 BOD and 84% of
the SS from. Incoming wastes. The batch processing system
offered by the Cromaglass units reduces the loading on the
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DIALOG Fllell: Pollution Abstracts - 7O-82/Apr (Copr Cambridge ScI Abs) (Item 4O of 98) User239l3 23JunB2
U)
o
o
8I-OO57S
Collection and analysis of purgeable organ I cs emitted from
wastewater treatment plants.
Pelltzzari, E. D.; Little, L.
Research Triangle Inst., Research Triangle Park, NC 277O9
U.S. ENVIRONMENTAL PROTECTION AGENCY. OFFICE OF RESEARCH AND
DEVELOPMENT. ENVIRONMENTAL PROTECTION TECHNOLOGY SERIES
Coden: EPTSBT Publ.Yr: Mar I98O
IIlus. IS refs.
Abs.
Languages: ENGLISH
An analytical method was developed for the analysis of
volatile priority pollutants In alrstreams passing through
wastewaters using a Tenax GC cartridge In combination with
GC-MS/computer. A sampling system was designed and Field
tested for sampling alrstreams passing through grit chambers
and activated sludge systems. Recovery of the volatile
priority pollutants was accomplished by thermal desorptlon,
purging with He Into a 1 Iquld-nl trogen-cooled Nl capillary
trap, and Introducing the vapors onto a GC column.
Characterization and quantification of the priority pollutants
was by MS using mass f ragmentography. The areas of
Investigation were as follows: the performance of a Tenax GC
sampling cartridge for the priority pollutants occurring In
the alrstreams passing through wastewaters; the design,
fabrication and evaluation of a field sampler; recovery
studies of priority pollutants from distilled water, raw
wastewater, and activated sludge using laboratory-simulated
conditions; a methods-of-addltIon study for priority
pollutants In raw wastewater and activated sludge; the
delineation of the GC/MS/COMP operating parameters for
priority pollutants collected on Tenax GC cartridges; the
application of the developed methods to the analysis of
priority pollutants; and evaluation of the accuracy and
precision of the collection methods for ''purgeable'' priority
pollutants In alrstreams from raw wastewater and activated
sludge basins. (AM)
Descriptors: Wastewater treatment plants; Engineering; Air
sampling; Activated sludge; Pollutant detection; Organic
compounds; Chemical analysis; Wastewaters; Gas chromatography;
Mass spectroscopy; Computer programs; Aromatic compounds;
Halogenated compounds
Identifiers: purgeable organIcs
8 I-OO564
Selected organic pesticides, occurrence, transformation, and
removal from domestic wastewater.
Saleh. F. Y.; Lee, G. F.; Wolf. H. W.
North Texas State Unlv , Denton, TX 762O3
WATER POLLUTION CONTROL FEDERATION. JOURNAL 52(1), 19-28,
Coden JWPFA5 Publ.Vr: Jan 1980
11lus. 16 refs.
Eng.. Fr.. Ger., Port., Span, abs
Languages- ENGLISH
Doc Type JOURNAL PAPER
A study was conducted on the characterization of chlorinated
organic pesticides In Dallas, Texas, municipal wasteuater.
The effects of biological wastewater treatment processes on
these compounds were also studied using a 3.785-m3/d nominal
capacity pilot plant with 2 activated sludge units.
Wastewater from different stages of treatment from a 2O4-ro3/d
overloaded high-rate trickling filter treatment plant was used
as feed to the activated sludge units. Analytical methods
Included electron capture GC on several columns of different
polarity and chemical derIvatIzatIon. Confirmatory tests,
e.g., TLC, extraction of p-value. and central processing
unlt-MS/GC, were used to confirm the compounds detected by
electron capture GC. Electron capture chromatograms of
wastewater showed characteristic fingerprints, consisting of
2O-25 peaks, which were constantly detected over a 2-yr
period. Thirteen compounds were confirmed. (AM)
Descriptors: Municipal wastewaters; Insecticides; Herbicides
; OrganochlorIne compounds: ChlorophenoxyacetIc acids: 2.4-D;
Dlazlnon; Organophosphorus compounds; Atdrln; DDE; DDT;
Pollutant detection; Pollutant removal; Wastewater treatment;
Texas; Biological treatment; Activated sludge process
Identifiers: Dallas; heptachlor epoxlde; 13 pesticides
81-OOSIO
Cooling-water treatment prevents excessive deposits.
Anonymous
CHEMICAL ENGINEERING 87(16). 91. Coden: CHEEA3
Publ.Yr: Aug II. 198O
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Phosphate-based treatments are now replacing the chromate-
or chromate/Zn-based cooling water additives used to protect
against corrosion and deposition for the past 3O yr. A
patented system-Dlanodlc II-Involves the use of 2 additives
Injected successively Into the cooling-water system. The
first additive contains orthophosphate, polyphosphate and
phosphonate compounds, and a Cu corrosion Inhibitor, while the
second contains an Inhlbltor/dlspersant for calcium
orthophosphate. The system improves corrosion protection
without excessive deposition and allows greater changes in
water chemistry without affecting the coating. Operating
costs are 45% less than that of the conventional chromate
treatment. (FT)
Descriptors: Cooling waters: Wastewater treatment: Corrosion
; Materials protection; Phosphates: Water pollutants
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DIALOG Flle41. Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 43 of 98) User23913 23Jun82
U!
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8 I -OO5O8
Evaluation of reverse osmosis membranes for treatment of
electroplating rlnsewater.
McNulty, K. J.; Hoover. P. R.
Abcor, Inc.. Maiden Dtv., Wilmington, MA OI887
U.S. ENVIRONMENTAL PROTECTION AGENCY. OFFICE OF RESEARCH AND
DEVELOPMENT. ENVIRONMENTAL PROTECTION TECHNOLOGY SERIES
Coden: EPTSBT Publ.Vr: May 198O
Illus. refs.
Abs. (Available from NTIS, Springfield. VA 22161)
Languages: ENGLISH
The RO system described functions by concentrating the
chemicals for return to the processing bath while purifying
the wastewater for reuse In the rinsing operation. The
effectiveness of the PA.-3OO. PBIL, NS-IOO. NS-2OO. SPPO. B-9,
and CA membranes were evaluated In tests on rlnsewater with
extreme pH and oxtdant levels. The PA-3OO membrane performed
well with copper cyanide. zinc cyanide, and chromic acid
rlnsewaters. while the NS-2OO and PBIL membranes performed
best with acid Cu rlnsewaters. After commercializing the
membranes, applications In various metal finishing,
non-ferrous metal, steel. and Inorganic industries may be
found. (FP.AM)
Descriptors: Reverse osmosis; Membranes; Wastewater
treatment; Metal finishing industry wastes; Waste treatment
Identifiers: electroplating rfnsewater
80-O8412
Management a control of heavy metals In the environment.
Anonymous
International conference: Management & control of heavy
metals In the environment London, England Sep 18-21. 1979
Commission of the European Communities-Institution of Water
Engineers & Scientists-Institution of Public Health
Engineers-Institute of Water Pollution Control-World Health
Organ)sat ion
664 pp Publ.Yr: 1979
Publ• Edinburgh, Scotland CEP Consultants
illus. index refs. for various papers
Abs.
Languages: ENGLISH
Doc Type: BOOK CONFERENCE PROCEEDINGS
Problems associated with management and control of heavy
metal-bearing wastes In marine, freshwater, and terrestrial
environments are discussed. Topics include health effects,
sources and pathways, analytical techniques, metal special Ion.
sludge treatment and disposal via land application. Industrial
sources, and waste management. The following metals are
considered: Cd. Pb. Zn. Kg, Se. Ag. As, V. Be. Co. Cr. N1, Sb.
Fe, Al, and Cu. (FP.FT)
Descriptors: Heavy metals; Waste disposal; Waste Management;
Marine environments; Freshwater environments; Terrestrial
environments; Toxicology; Public health; Measuring methods;
Sludge treatment: Sludge disposal; Land application;
Wastewaters; Books; Aquatic organisms; Sediments; Air
pollution; Conferences; Pollution control; Soils; Plants;
Chromium; Nickel; Antimony; Iron; Aluminum; Capper; Mercury;
Selenium; Silver; Arsenic; Vanadium; Beryllium; Mining;
Industrial wastes; Cadmium; Lead; Zinc; Cobalt
Identifiers: 16 metals; proceedings; metal speclatton
8O-O157O
Studies on the use of Inorganic gels In the removal of heavy
metals.
Srivastava, S. K.; Bhattacharjee, G.; Sharma, A. K.; Oberol.
C K.
Univ. of Roorkee, Chemistry Oept., Roorkee.
WATER RESEARCH 14(2). 113-I IS.
Publ.Vr: I98O
Illus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Chromium ferrocyanlde gel shows
Cu+2. Tit. Zn+2. CO+2, Cd+2. Mnt2.
to separate and recover some heavy metal ions. e.g.. T1+,
Hg+2, Mg+2. and Fe+3. Some of these can be completely eluted
from the columns of this exchanger material, and the compound
can be used to treat wastewater rich In heavy metal ions. The
only drawback of this material Is the partial recovery of a
few metal Ions, e.g.. Co+2, Cd*2. Mnt2, Zn+2, and Pb«2 and the
irreversible uptake of Cu+2 and Agt. (AM.FT)
Descriptors: Inorganic compounds; Ion exchange; Ions; Heavy
metals; Wastewater treatment; Silver; Copper; Thallium; Zinc;
Cobalt; Cadmium; Manganese; Iron; Mercury; Magnesium;
Contaminant removal
Identifiers: chromium ferrocyanide gel; distribution
coeff iclents
U.P.. India
Coden: WATRAG
great affinity for Ag*,
and Fe*3 and has been used
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DIAIOG Flle4l- Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 46 of 98) User239l3 23jun82
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O
K)
8O-O755I
Activated carbon process for treatment of uastewaters
containing hexavalent chromium.
Huang, C P.; Bowers. A. R
Univ. or Delaware, Newark, DE 19711
U.S. ENVIRONMENTAL PROTECTION AGENCY. OFFICE OF RESEARCH AND
DEVELOPMENT. ENVIRONMENTAL PROTECTION TECHNOLOGY SERIES
Coden. EPTSBT Publ.Yr: Jul 1979
Illus refs.
Abs (Available from NTIS, 6285 Port Royal Rd. .
Springfield. VA 22161)
Languages: ENGLISH
Doc Type- REPORT
The removal of Cr+6 from dilute aqueous solution by an
activated carbon process was Investigated. Two removal
mechanisms were observed- Cr+6 species were removed by
adsorption onto the Interior C surface and/or through
reduction to the trlvalent state at the external C surface.
The effects of Cr+6 concentrations, pH. C dosage, and extent
of mixing In the reaction vessel were studied In the batch
mode and In continuous flow packed column experiments In the
laboratory. The adsorptlve capacity of the C and the rates of
Cr+6 adsorption and reduction were determined. Thermal
regeneration of the exhausted C was examined, along with
caustic or acid stripping solutions and a combined
caustIc-thermal process. A case study Is presented and the
experimental data and rate expressions obtained from the data
are used to evaluate the design variables (pH. carbon dose.
Cr+6 concentration, and mixing In the reaction vessel).
Several Cr+6 treatment schemes are proposed, together with an
economic analysis of each scheme. (AM)
Descriptors: Wastewater treatment; Activated carbon;
Chromium; Heavy metals; Adsorption; Kinetics; Mathematical
analysis; Contaminant removal; Reduction; Economics
Identifiers: hexavalent Cr
8O-O752S
Examination of the applicability of cellulose Ion exchangers
for water and waste water treatment.
doergensen, S. E.
Royal Danish School of Pharmacy, Dept. of Chemistry AD, 2
Unlversltetsparken, DK-2IOO Copenhagen Oe, Denmark
WATER RESEARCH 13(12). 1239-1247, Coden: WATRAG
Publ.Yr 1979
Illus. refs.
Abs
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Three cellulose Ion exchangers were able to remove proteins,
azodyes. DBS. humlc acid, chromate. and heavy metal ions. The
selectivity of the Ion exchangers for removal of these
compounds Is very high, which explains their ability to remove
the examined compounds with high efficiency and capacity.
although the 3 cellulose Ion exchangers have only a small
capacity expressed as equivalents per liter. The mass
transfer coefficient was determined; only the Internal mass
transfer determines the uptake rate Theoretical column
calculations based upon the found mass transfer coefficients
were confirmed by pilot plant experiments (AM)
Descriptors: Ion exchange; Wastewater treatment; Water
treatment; Laboratory testing: Resins; Mathematical analysis;
Pilot plants; Feasibility studies
Identifiers: cellulose Ion exchangers; mass transfer
coef f Ic lent
8O-O751O
Processing chrome tannery effluent to meet best available
treatment standards.
Barber, L. K.; Ramirez, E. R.; Zemaltis, W. L.
A. C. Lawrence Leather Co., Inc., 1 Bridge St.. Winchester.
NH O347O
U.S. ENVIRONMENTAL PROTECTION AGENCY. OFFICE OF RESEARCH AND
DEVELOPMENT. ENVIRONMENTAL PROTECTION TECHNOLOGY SERIES
Coden: EPTSBT Publ.Yr: Jul 1979
Illus. refs.
Abs. (Available from NTIS. 5285 Port Royal Rd. .
Springfield. VA 22161)
Languages: ENGLISH
Doc Type: REPORT
To satisfy stream discharge requirements at its Winchester.
New Hampshire, chrome tan shearling tannery. the A. C.
Lawrence Leather Co.. Inc. selected primary and secondary
systems that are unique as applied to tannery effluent
treatment In the US. Primary clarification is accomplished by
means of coagulation and flotation, using electrolytic and
mechanical micro-bubble generation. The'secondary biological
section Is a CARROUSEL,TM a technical modification of the
Passveer oxidation ditch. During the 12-mo study. complete
analytical data representing winter and summer operating
conditions were acquired along with operating cost data. The
following parameters were analyzed. BODS; SS; N; NH3; Cr;
sludge volume; and fats, oils, and grease levels. These data
are presented and the design and operation of the system is
described. Possible applications of these principles to other
tannery wastewaters are suggested. (AM.FT)
Descriptors: Tanning Industry wastes; Wastewater treatment;
Water quality standards; Primary treatment; BOO; Secondary
treatment: Coagulation; Oxidation; Oils; Suspended solids;
Nitrogen; Ammonia; Chromium; Sludges
Identifiers: best available treatment; A. C. Lawrence
Leather Co., Inc.
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DIALOG F11e41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 49 of 9B) User239l3 23junS2
Ul
O
CJ
8O-O7458
Movement of heavy metals Into a shallow aquifer by leakage
from sewage oxidation ponds.
Ntssenbaum, A.; Wolfberg. A.; Kahanovlch. Y-; Avron. M.
Weizmann Inst. of Science. Isotope Dept., Rhovot. Israel
WATER RESEARCH 14(6), 675-679. Coden: WATRAG
Publ.Vr: I98O
Illus. rets
Abs.
Languages. ENGLISH
Doc Type- JOURNAL PAPER
The concentrations of Mn, Nl. Cu, Cd. and Cr were measured
In a shallow perched groundwater aquifer which underlies the
Dan Region Sewage Reclamation Project (Israel). The
contribution of effluents to the groundwaters has been
evaluated on the basis of C.I- concentration. Groundwater
containing >6O% effluents showed a lOO-fold decrease In Cu and
Mn 65O m away from the ponds, as compared with the near ponds
samples. Nickel and Cd showed only a small decrease In
concentration over 15O m. and then stayed constant. The*
concentrations of Cu and particularly of Mn In th^
groundwaters near the oxidation ponds Is equivalent to or
greater than In the ponds themselves. Copper and Mn are
mobilized from the precipitated sludge Into the Interstitial
waters. They percolate Into the groundwater near the ponds
and then are precipitated by Increasing aeration during the
movement of the water away from the pond area. Cadmium and Ml
form stable soluble organic chelates which are only slightly
removed by Interaction with the sandy soil of the aquifer. (
AM)
Descriptors: Groundwater: Aquifers; Israel; Effluents; Heavy
metals; Wastewater treatment plants; Sewage: Lagoons;
Activated sludge process; Manganese; Nickel; Copper: Cadmium;
Chromium; Chlorine compounds
Identifiers: Dan Region Sewage Reclamation Project
8O-O627O
The analysis and fate of odorous sulfur compounds In
wastewaters.
Jenkins. R. L ; Gute. J. P.: Krasner. S. W.; Balrd. R. B.
County Sanitation Districts of Los Angeles County. San Jose
Creek Water Quality Lab.. 1965 S Workman Mill Rd.. Whlttler.
CA 9O6O1
WATER RESEARCH 14(5). 441-448. Coden: WATRAG
Publ Yr: 198O
Illus. refs.
Abs.
Languages• ENGLISH
Doc Type: JOURNAL PAPER
GC coupled with the S-speclflc flame photometric detector
was used as the basis for developing an analytical system with
sensitivity In the ppb (mL odorEint/mL air) range for
organosulfur compounds. A high vacuum line for storage and
handling of standard compounds, and the use of gas syringes
are Integral features of the calibration system. Sampling
equipment was constructed and tested which allows the analysis
of gaseous organosulfur compounds In wastewaters, sewer gases,
and ambient air. Gaseous mixtures keep better than aqueous
solutions with respect to microbiological, chemical, or
physical losses. The analytical system was employed to trace
and characterize an odor Incident from a municipal treatment
plant to the Industrial discharger causing the problem.
Certain long-chain mercaptans which are not normally odorous
can decompose In aeration treatment facilities to produce low
molecular weight mercaptans which then cause an odorous
condition. (AM)
Descriptors: Odors; Sulfur compounds; Wastewaters; Pollutant
analysis; Gases; Organic compounds; Laboratory methods;
Organosulfur compounds; Gas chromatography
Identifiers: flame photometric detector
8O-O623!
A practical approach to Wastewater treatment for the metal
finishing Industry.
Olthof, M.
Duncan, Lagnese and Assoc , Inc.. 3185 Babcock Blvd..
Pittsburgh. PA 15237
WATER POLLUTION CONTROL ASSOCIATION OF PENNSYLVANIA.
MAGAZINE 12(6). 18-27. Publ.Yr: Nov-Oec 1979
11lus. no refs.
No abs.
Languages: ENGLISH
Ooc Type: JOURNAL PAPER
General guidelines for the development of a pollution
control program for a metal finishing plant are provided.
In-plant considerations for the design of a treatment ' system
Include water flow reduction, optimizing the dilution ratio.
counterflow rinsing, cascade rinsing. segregation, process
solutions, floor spillage, and dragout reduction. Practical
treatment methods Include hexavalent chromium treatment.
cyanide treatment, and general rinse water treatment.
Reference Is made to promising new technologies and their
potential application. The chemistry outlined forms the basis
for the design of Wastewater treatment facilities. A typical
flow schematic for a metal finishing plant Is presented.
Miscellaneous treatment approaches Include Integrated system.
Ion exchange. and RO. The potential for recovery of one of
the plating solutions should be evaluated during the planning
stage for pollution control facilities; Nl, Cr. Cu, and Zn
plating baths are possibilities. (FT)
Descriptors: Metal Industry wastes; Wastewater treatment;
Pollution control; Engineering; Ion exchange; Reverse osmosis;
Chromium; Cyanides
Identifiers. metal finishing Industry; hexavalent Cr
treatment; cyanide treatment; general rinse water treatment
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DIALOG Flle4t. Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 52 of 98) User23913 23junB2
CO
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80-O6157
Treatment of dilute metal effluents In an electrolytic
preclpttator.
Brysort. A. W ; Oardis. K. A.
Univ. of the Wltwatersrand, Dept. of Chemical Eng., Jan
Smuts Ave , Johannesburg 2OO1, South Africa
WATER S. A 6(2). 85-87. Coden; WASADV Publ.Yr: Apr
)98O
I1lus. refs.
Abs
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Excessive concentrations of metals (n industrial effluents
may adversely affect the performance of sewage purification
works A1though there is exist Ing technology for treat ing
these effluents, It has not found wide application due to
costly equipment and chemicals and the absence of sufficient
space on most plants. The feasibility of removing these
metals from dilute solut ions by electrolytIc precfpltat ion
using a parttculate electrode Is investigated. A test plant
wa s cons t rue ted wh1ch was compact, did no t requt re the
addition of chemicals and could be operated by unskilled
personnel. The plant was Installed at an electroplating works
on the Wi twatersrand and was successful In treat ing wash
waters containing Cu, Nl, Cr, and 2n. (AM)
Descriptors: Heavy metals; Electric collectors; Industrial
effluents; Wastewater treatment; Nickel; Nickel; Chromium;
Copper; 2inc; Engineer ing; South Africa; Sewage treatment;
Feasibility studies
Ident If iers: Johannesburg; electrolyt1c preclpi ta tor
8O-O4555
Effects of treated effluent on a natural marsh.
Murdoch. A.; Capobtanco, J. A.
Canada Centre for Inland Waters, Process Research O*v.,
Geology Section. P.O. Box 5O5O. Burlington, Ontario L7R 4A6.
Canada
WATER POLLUTION
2243-2256. Coden:
51(9).
CONTROL FEDERATION. JOURNAL
JWPFA5 Publ.Yr: Sep 1979
11lus. refs.
Eng. . F r . Ger., Por t. . Span. abs.
Languages- ENGLISH
Doc Type: JOURNAL PAPER
Long-term effects of poor-quality wastewater treatment plant
effluent on a natural marsh on the western shore of Lake
Ontario were studied. The major contributor of N and P to the
marsh area was the treatment plant discharge. Metal
concentrat ions In the water were generalty low
(<1X1O-3-9OXIO-3 mg/L). Increased concentrations of Pb. Cr,
Zn, N, P, and organic C (<=3OO mug/g, 9O mug/g, 21O raug/g,
2.34%. 1.1O%, and O.87% of sediment dry weight, respectively)
were found in the sediment vert leal prof lie obtaIned from the
marsh area. The shoot standing crop of the dominant plant
spec Ies (Glycerla grand Is) was assoc(ated with amounts of P,
N, and organic C In the sediments. (AM)
Descr iptors: Wastewater discharges; Wet lands; Lake Ontarlo;
N11rogen; Phosphorus; Lead; Chrom1um; Z i nc; Carbon; Sed(men t s;
Plants; E nvIronmen t a 1 1mpac t; Nutrients
Identifiers: Glycerla grandis
of Wastewater (n the presence of
, USSR
No.
3.
9-11.
developed for comparat ive
posslb11 Ity of var fous
in wastewater purification.
8O-O34iO
(Biological purification
chemically bonded oxygen).
Karyukhlna. T. A,; Ksenofontov, V. A,
Kulbysheva Moscow Eng. Construction Inst
VOOOSNAB2HENIE I SANITARNAIA TEKHNIKA
Coden: VSTEAO Pub!.Yr: 1979
illus refs.
abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Thermodynamlc equat Ions were
assessment of ttie theoret ical
biochemical processes for use
Biochemical reduction of O-contatnlng anIons of Group III-VII
elements In the periodic table under anaerobic conditions was
accompan1ed by decreases 1n the concent r a 11on of organ i c
pollutants, dlssoclat ion of anIons. and the part la 1
demineralIzation of wastes. The calculations showed the
possIbl1i ty of biochemical reductIon of chromates and
bichromates. sulfates, nltrates. carbonates. selenates,
tellurates, tungstenates, and vanadates. For the f trst t troe,
lodates and bromates were reduced experimentally; the rate of
reduction of bromates was 3 mg O/g/hr of ash-free sludge while
that for lodates was 2.8 tng/g/hr. (AM.FT)
Descriptors: Wastewater treatment; Oxygen compounds; An Ions;
B1 o 1 og ical ox i da t * on; Chetn teal
ana lysis
IdentIfIers: anion reductIon;
nl trates; carbonates; selenates;
vanadates
treatment; Matheroatteal
chromates;
tellurates;
b ichromates;
tungstentes;
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DIALOG F1le41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 55 of 98) User239l3 23jun82
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8O-O3296
Analysis of selected trace organlcs In advanced wasteuater
treatment systems.
Bat id, R. ; Se,lna. M. ; Mask Ins, J.; Chappelle, D.
Los Angeles County Sanitation Districts. San dose Creek
Water Quality Lab.
9OGOI
WATER RESEARCH
Publ.Yr:
Illus.
1965 S. Workman Mill Rrt
Whlttler. CA
13(6). 493-5O2. Coden: WATRAQ
1979
• refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Effluents through 4 different pilot tertiary wastewater
treatment systems were monitored for selected trace organic
compounds. The effects of using O3. and free and combined Cl
residuals In these systems were studied. Advanced treatment
of secondary effluent using various combinations of
flocculatlon (alum and polymer), dual media filtration, and
carbon adsorption were evaluated for production or removal of
volatile halogenated organlcs. PAHs, chlorinated pesticides,
and PCBs. GC methods were used; specific techniques and
analytical parameters are described. Salient results Included
drastic Increases In tr lhalomethane production using free Cl
residuals: no significant levels of trlhalomethanes with
disinfection using combined Cl species: =90% reduction In
tr lha lomethane levels by carbon adsorption; absence of
detectable quantities of PAHs; and significant decreases In
pesticide and PCB levels by carbon adsorption and
chlor Inat Ion. Statistical dependence of tr lha lomethane
production on soluble COO, SS. and chloramlne levels was
evident from multiple linear regression calculations. (AM)
Descriptors. Chemical analysis; Wastewaters; Organic
compounds; Gas chroma tography; Wastewater treatment;
Disinfectants; Aromatic compounds: PCB compounds; Pesticides
Identifiers: trlhalomethanes
for N removal, recarbohatIon and filtration. activated-carbon
adsorption for organlcs removal. RO for demlneralIzatIon. and
final chlorInatIon for disinfection. The COD and a broad
range of volatile and gas chromatographable substances were
measured In the plant Influent and effluent and In the
effluents of Individual processes. Lime treatment was
effective In removing COO and PCBs. while NH3 stripping and
activated-carbon contacting removed a broad range of volatile
compounds. Chlorlnatlon led to the formation of a variety of
halogenated compounds, mainly trthalomethanes. (AM)
Descriptors: Wastewater treatment plants; Water treatment;
California; Organic compounds; Pollutant removal: COO: Heavy
metals; Suspended solids
Identifiers. Water Factory 21; Orange Co.
BO-O32O4
Trace organlcs removal by advanced waste treatment.
Reinhard. M.; Dolce, C. J.; McCarty, P. L.; Argo, 0. G.
Stanford unlv . Dept. of Civil Eng.. Stanford. CA 943O5
91st annual meeting of the AOAC: Symposium on environmental
contamination by Industrial organic chemicals Washington, DC
Oct 1977
AMERICAN SOCIETY OF CIVIL ENGINEERS. ENVIRONMENTAL
ENGINEERING DIVISION. JOURNAL t05(EE4). 675-693. Coden:
JEEGAV Publ.Yr: Aug 1979
11lus. refs.
Abs.
Languages ENGLISH
Doc Type: JOURNAL PAPER CONFERENCE PAPER
The performance of an advanced waste treatment plant. Water
Factory 21, In Orange County, California, was Investigated
with respect to organlcs removal. The processes for treating
trIckIIng-f11ter effluent were lime treatment for SS and
heavy-metal removal. NH3 stripping and breakpoint Chlorlnatlon
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DIALOG rile41 Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sol Abs) (Item 57 of 98) User23913 23jun82
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o
(T.
&
Feb
TECHNOLOGY
1979
13(2).
I6O-164,
I .(INVESTIGATIWE/OBSER-
BO-O1973
Textile plant wastewater toxlclty.
Rawlings. G. D.; Samfteld. M.
Monsanto Research Corp., Dayton, OH 454O7
ENVIRONMENTAL SCIENCE
Coden: ESTHAG Publ.Yr:
I I Ins refs.
ISSN: OOI3-936X
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: O .(DESCRIPTIVE)
VATION)
The American Textile Manufacturers Institute 1O, and are then oxidized to N and CO2 with the NaOCI
solution at pH 8.5. When the ORP reaches a range of 35O-4OO
nV (indicating that all cyanides have been oxidized) the
wastewater changes from a clear. transparent green to sky
blue. Complete oxidation takes MO mln. The treated water Is
allowed to settle for =2 hr, during which time small amounts
or metals, e.g., Cu and Ag. will be precipitated as Insoluble
hydroxides. (FT)
Descriptors: Industrial wastes; Wastewater treatment;
Chromium; Cyanides; Precipitation; Chemical oxidation;
Reduction; pH; Metals; Toxic materials
Identifiers: electroplating rlnsewaters; automated control;
sodium bisulfite; sodium hypochlorlte: hydroxides
toxic electroplating
INWABK
BO-O1928
Methods for neutralizing
rlnsewatei—part 3.
Marln, S.: Trattner. R. B.; Cheremlsinoff. P. N.
New Jersey Inst. of Technology, Newark, NJ O7IO2
INDUSTRIAL WASTES 25(5), 22-23, Coden
Publ.Yr Sep-Oct 1979
rcfs. i
ISSN: 0537-5525
No atos.
Languages: ENGLISH
Doc Type. JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; D .(DESCRIPTIVE)
In the removal of Cr from electroplating rlnsewater,
treatment Is intended to convert Cr+6 to Cr+3, and then
the
to
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DIALOG File41. Pollution Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 59 of 98) User23913 23jut)82
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8O-OI89I
IBM Ouego give metal finishing wastes total treatment.
Forbes. J. M.
IBM, Owego. NV 13126
POLLUTION ENGINEERING 11(3). 46-49, Coder): PLENBW
Publ.Vr- Mar 1979
I Mus. no ref s.
ISSN: OO32-364O
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: A (APPLICATIONS) ; N .(NEW DEVELOPMENTS)
IBM's Federal Systems Division facility at Owego, New York.
has various plating and metal finishing operations Including
copper plating, cleaning, surface treatment, and etching, with
associated rinses that generate =5OO.OOO gpd of wastewater.
At the main facility there are 3 prime Industrial drain
systems, a general rinse drain for nonchrome, noncyanlde rinse
waters, an acid-alkali drain for Intermittent small volume
batch dumps of acids and alkali cleaners, and a chrome drain
to receive chrome waste rinse waters. The chrome and
acid-alkali wastes are pretreated before entering the general
rinse system. The general rinse system alone handles the bulk
of the wastes and begins with the collection and equalization
of wastes In a 5OO.OQO-gal lined lagoon. After passing
through a settling and skimming tank, the general rinse passes
through a demlneral tzer-neutral tzat Ion tank to two SOO-gpm
clariflers for removal of the metallic hydroxides and SS by
the filtering action of a sludge blanket. Results from the
past 2 yr have shown very successful system operation. with
effluent standards well within EPA limits. (FT)
Descriptors: Wastewater treatment; Wastewater treatment
plants; Engineering; New York; Pollutant removal; Metal
finishing industry wastes
Identifiers. IBM's Federal Systems Division; Owego
oxidation by sodium hypochlorlte or C12 plus sodium hydroxide
addition to the waste. Electrolytic decomposition and
ozonation are also effective treatments for cyanide wastes.
Chromium waste treatment Involves reduction and precipitation
processes Reducing agents Include ferrous sulfate. sodium
blsulfate. and sulfur dioxide; neutralizing compounds include
lime slurry or caustic. Batch treatment Is necessary In shops
having a total datly flow <3O,OOO gpd, whereas continuous
treatment Is recommended for volumes >3O.OOO gpd. (FT)
Descriptors: Metal finishing Industry wastes; Cyanides;
Chromium compounds; Wastewater treatment; Contaminant removal;
Chemical oxidation: Neutralization; Reduction
Identifiers: electroplating
8O-O1866
Methods for neutralizing toxic electroplating
rlnsewater-part t.
Marln. S.; Trattner, R. B.; Cheremlslnoff. P. N.; Perna. A.
J
New Jersey Inst. of Technology, Newark, NJ O71O2
INDUSTRIAL WASTES 25(3), 5O-52. Coden. INWABK
Publ.Yr. May-Jun 1979
11lus. no refs.
ISSN: O537-5525
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; A .(APPLICATIONS) ; D
.(DESCRIPTIVE)
Rlnsewaters from the electroplating process contain high
concentrations of cyanides and chromates. To comply with US
EPA discharge standards several chemical processes have been
developed to destroy the cyanides and chromates. For cyanide
the most common form of treatment is alkaline chlorlnation
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DIALOG Flle4t Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc I Abs) (Item 61 of 98) User23913 23JunB2
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00
80-OI412
The EPA-proposed granular activated carbon treatment
requirement: Panacea or Pandora's box.
Peridygraf t, G. W. ; Schlegel . f E . ; Huston, H. J.
Baker ft Daniels
AMERICAN WATER WORKS ASSOCIATION. JOURNAL 71(2), 52-6O.
Codeii: JAWWA5 Publ . Vr : Feb 1979
no refs.
ISSN- OOO3-15OX
No abs.
L anguages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: D .(DESCRIPTIVE) ; N .(NEW DEVELOPMENTS)
The feasibility of GAC treatment to accomplish the EPA's
desIred goal. a substantlal reductIon or removal of trace
amounts of synthetic organic chemicals (SOCs) In publIc
drinking supplies. Is questioned. No water system In the
world has used GAC treatment to satisfy the design criteria
prescribed by the proposed regulation. Although the European
GAC practice has been cited as support for the EPA-proposed
GAC requlrement. scrutIny demonstrates that rIver bank
f11tratIon or ground passage. not carbon treatment, Is
respons1b1e for much of t he organ1c remova1 In European
waterworks. The use of GAC for taste and odor control has
little. If any. bearing on Its efficacy to control organlcs.
The use of GAC In the food and beverage Industry.
Pharmaceuticals, municipal, and Industrial wastewater
treatment Is examined. Six alternatives to GAC are suggested.
Additional research Is needed to evaluate the chrotnatographtc
or desorptlon effects of GAC. GAC Itself may be a source of
harmful chemicals. Its large surface area providing a site for
many undesirable chemical reactions and an Ideal location for
bacterial growth that would subsequently be released Into the
fIna1 drink Ing water. The fInanetal effects and energy
consumptIon problems are examined. Engineers and cancer
specialists overwhelmingly oppose the regulation. (FT)
Descriptors: Act Ivated carbon; EPA; Water pur If leatIon;
PublIc concern; Feasibility studies; Federal regulatIons;
Economics; Engineering; Organic wastes; Water treatment plants
; PublIc health
Identifiers- trlhalomethanes; synthetic organic chemicals;
granular activated carbon; health risks
79-O6664
Residual heavy metal removal by an algae-Intermittent sand
filtration system.
FfHp. 0. S ; Peters. T.; Adams, V. 0.; Mlddlebrooks, E. J.
Utah State Unlv , Utah Water Research Lab. , Logan, Uf 8-1322
WATER RESEARCH 13(3), 305-313, Coden- WATRAG
Publ.Yr. 1979
11 Jus. refs.
Abs.
Languages ENGLISH
Doc Type. JOURNAL PAPER
A 1aboratory scale study was undertaken to determine the
feasibility of using algae growing In wastewater lagoons to
absorb res Idual heavy metals for subsequent complete remova1
by Intermittent sand filtration of the metal laden algae. In
semicootInuous cut tures the mixed algal fI ora natIve to
wastewater lagoons absorbed 7O% 9O% of the Cd and Cu from the
wastewater media. Chromium absorption was less by ratio (2O%
was absorbed), but the mass of Cr removed was much greater as
high levels of Cr were added. Only 1 alga (Osci1latoria sp. )
which was extremely resistant to Cr grew in the Cr exposed
cultures. Nearly total removal of the Cd and Cu was achieved
by the algae-Intermittent sand filter system. The net Cr
removal agreed with the accumulation analyses. (AM)
Descr iptors: Heavy metafs; Lagoons; Algae; Wastewater
treatment; F11tratIon; Copper; Cadmium; Chromium; Feas ibl1 Ity
stud1es; Contarn1nant remova1
79-O6658
Instrumental analysis In wastewater treatment.
McLean. D. A.; Phillips. S. L.
East Bay Municipal UtIIIty District. P.O. Box 24O55,
Oakland, CA 94623
ANALYTICAL CHEMISTRY 5O(14). 136IA-I376A, Coden:
ANCHAM Publ.Vr: Dec. 1978
11lus. refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The development of was tewa ter trea tment 1s rev 1ewed.
emphasizing the analytical methods used to monitor the
treatment processes. Early methods of analysis were manual,
I.e., gravimetric. tttrlmetrlc. and visual comparI son, and
rudimentary InstrumentatIon. The advent of AAS and GC
provided methods by which Individual elements or compounds
could be analyzed with high specificity and sensitivity.
Heavy metals could be analyzed for at low concentrations In
samples that contained high levels of Interfering substances.
Trace organic compounds were analyzed with developing GLC and
gas-sol Id chromatography technology; the analysIs of
chlorInated pestIcldes and polyentorInated aromat ics became
possible with the development of thermal conduct Ivlty; flame
lonlzatlon, electron capture, and alkali flame GC detectors.
Ins trumen taI methods whIch have been used the 1onges t 1n
mon1 tor 1ng was tewa ter treatment processes i nc1ude pH,
conduct ivity, ox idatIon-reduct ion potentlal, OO, turbidlty.
and Cl residual analysis (FT)
Descriptors: Wastewater treatment; Moni tor ing methods;
Chemical analysis; Hlstorleal rev lews
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DIALOG Flle41 Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 64 of 9B) User239l3 23Jun82
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79-O6647
Investigation of soluble organic nitrogen compounds In
municipal secondary effluent.
Keller, J. V ; Leekte, J. O.; McCarty. P. L.
James M. Montgomery Consulting Engineers. Inc., 199O N.
California Blvd., Suite 444, Walnut Creek, CA 92707
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5O(11),
2522-2529. Coden: JWPFAS Publ.Vr: Nov. 1978
Itlus. refs.
Eng., Fr., Ger., Port., Span. abs.
Languages: ENGLISH
Doc Type. JOURNAL PAPER
The ability of anlon and cation exchange resins and granular
activated carbon to remove soluble organic nitrogen and other
soluble organIcs from fIItered municipal activated sludge
effluent was studied Ion exchange, particularly using cation
exchange res 1ns, couId be used as an expens\ve po11sh f ng
treatment to remove N5O% of the soluble organic fraction
remaInlng af ter adsorptIon wlth high dosages of act fvated
carbon. Before and after activated carbon contacting of
secondary effluent, more of the soluble organic nitrogen was
positively charged, and more of the soluble COD was negatively
charged, Sephadex column chromatography indicated that
activated carbon contacting removed a significant fraction of
the soluble organic nitrogen and soluble COO present In
secondary effluent. (AM)
Descr(ptors: Resins; Ion exchange; Act fvated carbon;
Wastewater treatment; Nitrogen; COD; Activated sludge process;
AdsorptIon; Tertlary treatment
Identifiers: anlon exchange resins; cation exchange resins
79-O6623
Treatablllty evaluation of general organic matter. Matrix
conception and Its application for a regional water and waste
water system.
Tarobo, N.; Kamel, T.
Hokkaido Univ., Faculty of Engineering, Dept. of Sanitary
Engineering. Sapporo, O6O Japan
WATER RESEARCH 12111), 931-95O, Coden: WATRAG
Publ.Yr- 1978
1\lus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Group Ing of organic compounds In wastewater treatablItty
evaluation can be performed by gel chromatography. Using
Sephadex G 15 gel with 2-stage elutlon of distilled water and
O. IM ammonium hydroxide solution, general organic compounds In
a regional water and wastewater system are characteristically
grouped Into 6 groups. The treatabt11ty of each group Is
characterized by the ratio of TOC:E 26O (UV absorbance at 26O
nro). Only a port Ion of TOC, which is Insens11Ive to UV
absorbance at 26O nm, can effectively be removed by aerobic
bIo1og1ca1 processes Sma11 organ ic compounds are
b iologlcalIy decomposed readlly unt11 TOC:E 26O rat to of
4O-5O'1 Is obtained Large organic compounds are effectively
removed by coagulation with Al followed by sedimentation and
sand f 11tratIon. For smaIler organic compounds. coagulatIon
Is Ineffective; activated carbon adsorption Is effective for
TOC: E26O ratios of N5O.' (MS)
Descr tptors: Wastewater treatment; TOC; Ultraviolet
radiat1on; Biological treatment; Physicochemlcal treatment;
Engineering; Liquid chromatography; Organic compounds
Ident 1flers: treatablllty criteria; gel chromatography
79-O5437
Direct analytical procedure for determination of volatile
organic acids In raw municipal wastewater.
Narkls, N.; Henf eld-FuMe. S.
Technlon-Israel Inst, of Technology, Environmental
Engineering Labs.* Technlon City, Haifa, Israel
WATER RESEARCH 12(7), 43T-446. Coden: WATRAG
Publ.Vr: 1978
11lus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
A direct analytical method for 1dent If teat Ion and
determtnatIon of the Individual volatIle acids In raw sewage
was developed- The proposed procedure Is rapid, omitting
tedious sample pretreatment, and thus avoiding possible losses
Involved In steam distillation. evaporation, or extraction.
Raw sewage Is directly Injected Into a gas chromatograph. with
Carbowax 20 M on acid washed Chromosorb W column and a flame
lonlzatIon detector. Sample preparetIon Is confIned to
addition of solid metaphosphorIc acid to the raw sewage, and
removal of precipitated proteins and SS by centr1fugation.
Volat1le acids content tn raw muntcIpal sewge In Ha 1 fa,
Israel. was »n the range of ISO-16O mg/L, of which 12O-125
mg/L was acetic acid, 3O-33 mg/L proplonic acid, 6-8 mg/L
butyric acid, 2 mg/L Isovaterlc acid. and O.5-1 mg/L valeric
acid. (AM)
Descriptors: Gas chromatography; Ac 1ds; Sewage; IsraeI
Ident Iflers: Ha ifa; acet tc acId; proplonic acid; butyrIc
acid; Isovalerlc acid; valeric acid
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DIALOG F11e41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 67 of 98) User23913 23Jun82
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M
O
79-OS426
Effects of chlorlnation of some volatile organIcs in primary
municipal sewage effluent.
Mori. B. T.; Hall. K. J.; Blazevlch. J. N.
Health and Welfare Canada, Health Protection Branch. 1OO1 W-
Pender St.. Vancouver, B.C.. Can.
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH. PART A:
ENVIRONMENTAL SCIENCE AND ENGINEERING A 13(7). 445-467,
Coden: JESEDU Publ.Vr: 1978
i1lus refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The effects of chlorlnation on volatile organic components
of prImary municipal sewage effluent were Invest Igated.
Primary sewage effluent had TOCs of 5O mg/L after filtration
through 1 1 glass fitters and 38 mg/L after filtration through
O.45 1 membrane filters. Chlorine doses of O-1O3 mg/L had no
measurable effect on the TOC value. GC-electron capture
analysis Indicated that 19-21 new peaks consistently resulted
from chlorlnatlon at treatment plant dosages. Seventeen to 19
of these peaks were neutral or basic compounds. GC with a
microelectrolyt Ic conductIvt ty detector demonstrated that
O.OI% of the Cl applied to primary effluent at treatment plant
levels ends up In stable, volatile chlorInated organic
compounds. Furthermore, 4O% of the volatile organically bound
Cl In chlorinated-dechlorInated primary effluent resulted from
the chlorlnation process. Three of the compounds resulting
f rom ch1 or\na 11on, I.e., ch1orobenzene. 1.3-dIch1orobenzene
and a-chlorotoluene. were positively Identified by GC-MS. The
•concentrations of these compounds were in the Ig/L range; 61
other compounds were also Identified with varying degrees of
certainty. None of these latter compounds appeared to be
formed by the chlorInalion-dechlorInatIon process. (AM)
Descriptors: Chlorlnation; Municipal wastewaters; Sewage
treatment; Gas chromatography; Mass spectroscopy; Wastewater.
treatment
removed from the filter as a slurry With decreasIng
hydraulIc detent Ion t ime the metal remova1 percentage
decreased while the metal content In the bottom slurry
Increased. Most metals were removed In the lower port Ion of
the f 11ter. Copper was assoclated wlth the largest sol Ids
part Ides, but also showed the largest var tat Ion In
concentratIons and largest decrease In removal eff fc fancy at
decreasing hydraulic detention times. (AM)
Descr iptors: Copper; Zinc; Nickel; Chromium; F1 Iters;
Anaerobic systems; Heavy metals; Wastewater treatment
IdentIfiers. metal removal
79-O4165
Heavy metal removal with completely mixed anaerobic filter.
DeWalle. F. B.; Chlan. S. K.; Brush. J.
Univ. of Washington. Oept, of Environmental Health. Seattle.
WA 98IO5
WATER POLLUTION CONTROL FEDERATION. JOURNAL 51(1). 22-36,
Coden: JWPFA5 Publ.Yr: Jan. 1979
11lus refs
Eng.. Fr.. Ger., Port.. Span, abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
A completely mixed anaerobic filter was subjected to various
leachate loadings. At each detention time samples were taken
from the Influent, effluent, and other sampling ports for AAS
heavy metal analysis. The fitter was effective In removing
heavy metals, the effectIveness increasing with increas ing
meta I concentratIons In the effluent The metals were
precipitated as sulfides. carbonates. and hydroxides and were
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TECHNOLOGY
1978
Plating Effluent Treatment
12(8),
896-899.
79-O2832
A clean water project In Poland.
KleszkowskI. M.; Jackson. G. S.
Inst. of Precision Mechanics,
Dept., OO-967 Warsaw. Pol.
ENVIRONMENTAL SCIENCE &
Coden. ESTHAG Publ.Vr: Aug.
Illus. refs.
Sum.
Languages: ENGLISH
Ooc Type JOURNAL PAPER
Wastewaters produced In metal finishing operations contain
such pollutants as cyanides, chromates. heavy metals. mineral
acids. alkalis, oils. greases. detergents, and organic
solvents. The most common effluent treatment consists of
well-known, conventional chemical procedures which can be done
either continuously or batch-wise. They Involve several
operations, such as alkaline chlorlnatlon of segregated
cyanide solutions, reduction of segregated chrornate solutions,
and final neutralization of mixed effluents and precipitation
of metal hydroxides. followed by land fill disposition. A
schematic diagram of such an effluent treatment plant Is
presented. Applied research for the Polish metal finishing
Industry Is conducted by the Institute of Precision Mechanics,
In Warsaw, which has developed several new effluent treatments
and material recovery techniques. The most promising Include
evaporative recovery of plating bath constituents from rinse
waters, RO systems for some plating solutions, Improved Ion
exchange systems for single metal recovery from separated
rinse streams, secondary polishing systems for final effluent
purification. rinse water purification steps prior to
evaporative recovery of RO. foreign metal recovery and other
impurity removal from metal finishing solutions.
ultrafIItratlon methods for water reclamation. and
solidification of metal finishing sludges containing mixed
metallic hydroxides. Other promising techniques Include
possible utilization of sulflde precipitation of heavy metals.
solvent rinsing. Ion flotation, C adsorption, and recovery of
metals from hydroxide sludges by solvent extraction (FT)
Descriptors: Metal finishing Industry; PollutIon control;
Materials recovery; Reverse osmosis; Ion exchange; Engineering
; Cleaning process; Heavy metals; Poland
Identifiers plating Industry: Polish Institute of Precision
Median Ics
JFRBAK Publ.Yr: May 1978
Illus refs.
Eng.. Fr. abs.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
The petroleum hydrocarbon content of sediment cores
collected from Narragansett Bay and Rhode Island Sound were
compared to a relatively unpolluted sediment core from the
Gulf of Maine. Organic components were extracted from the
saponified sediment using a toluene*methanol mixture and
separated by column chromatography and TLC. GLC analysis
identified and quantified 3 hydrocarbon types, unbound. bound
or associated with the clay mineral or kerogen matrix, and
bound or associated with humlc substances. In general
9O%-1OO% of the hydrocarbons were. In the unbound form and
could be easily extracted with organic solvents. The
petroleum hydrocarbons decreased with depth at all stations.
Blogenlc hydrocarbons (nC25. tiC27. nC29, and nC31) made up an
Increasingly greater percentage of the total with increasing
depth. The hydrocarbons In the Narragansett Bay sediments and
near surface Rhode Island Sound sediments strongly resembled
the hydrocarbons previously reported for the Providence River
and upper Narragansett Bay. These petroleum-I Ike hydrocarbons
were largely Introduced to the river and bay through chronic
Inputs from a municipal wastewater treatment plant. The
hydrocarbons then undergo sedimentation throughout the entire
bay and Into Rhode Island Sound. Preliminary calculations
Indicate that KO.2 million t of petroleum hydrocarbons may be
transported to the marine environment annually from municipal
treatment plants. Most of these hydrocarbons appear to
accumulate In estuartne and coastal sediments. (AM)
Descriptors: Sediments; Petroleum; Hydrocarbons; Wastewater
treatment plants; Municipal wastes; Marine environments;
Estuaries; Rhode Island; Chromatography
Identifiers: Narragansett Bay; Rhode Island sound;
Providence River; Gulf of Maine
79-O1659
Contribution of chronic petroleum Inputs to Narragansett Bay
and Rhode Island Sound sediments.
Van Vleet, E. S.; Oulnn, J. G.
Univ. of California at San Diego. Inst. of Marine Resources,
La Jolla. CA 92O93
Symposium on recovery potent la
environments Halifax. N.S , Can.
Recovery potential of oiled marine northern environments.
Symposium papers. Edited by j; C. Stevenson. In CANADA
FISHERIES RESEARCH OOARD. JOURNAL 35(5). 536-543. Coden
of oiled marine northern
Oct. 1O-14. 1977
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DIALOG FMe4t Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 7t of 98) User23913 23junB2
79-OO626
Wastewater from platfng works-required pretreatment and
disposal of concentrates.
Imhoff, K. R
Ruhrverband und Ruhrtalsperrenverein, Kronpr inzenstrasse 37.
43OO Essen I, FRG
International conference on advanced treatment of wastewater
Johannesburg. S. Afrlea June 13-17, 1977
Advanced treatment and reclamation of wastewater: Conference
proceedings. In PROGRESS IN WATER TECHNOLOGY 1O(1-2),
419-43O, Coden: PGWTA2 Publ.Vr: 1978
Ulus. refs. (Some In Ger. )
Sum,
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
The Ruhrverband ensures that the wastes of metal finishing
establ ishments In the Ruhr catchment are recycled to the
chemical Industry; the sale of the wastes covers only
transportatIon costs, but there are savings compared to
chemical prectpltat Ion and sludge disposal. Wastewater Is
treated In 118 mostly small plants. Cyanide and
chroinate containing wastewaters must be collected separately
and pretreated. The central decontamination plant at
Iserlohn. and the central treatment plant at Helllgenhaus are
described. To supplement the system of wastewater treatment
plants 4 Impoundments were constructed In the Ruhr valley.
The central wastewater treatment plants ellmlate 6O% of the
Influent heavy metals. During low flow In the lower Ruhr
river a ratio between clean water and treated wastewater of
7O:3O Is malntaIned on the average. From this mixture
waterworks abstract their water and prepare drinking water by
artificial groundwater recharge. (FT)
Descriptors: Federal Republic of Germany; Metal finishing
Industry wastes; E ffluent treatment; Wastewater treatment
plants; Industrial effluents; Municipal water supplles; Waste
reuse
Ident 1f1ers Ruhr vaI Iey
Increase the reaction rate; add a reducing agent; raise pH OB
to precipitate chromium hydroxide; and clarify the effluent to
minimize chromium hydroxide carryover. A several fold excess
of reduc fng agent 1s requIred to reduce the chroma te
quantitatively. The amount of acid, reducing agent, and
alkali vised is a function of the complete chemical composition
of the blowdown. the reducing agent used. and the discharge
restr1ctIons. Electrochemlcal reductIon Involves a series of
Fe anodes connected to an electrical source; the block of
anodes is placed In a reservoir through which the blowdown
flows. Efficiency of chromate removal Is decreased when other
oxidizing agents are present In solution. A conservative
estimate of electrode usage Is 4 Ib/lb of Cr. Current flow,
arrangement of electrodes. and level of gas-1tquid Interface
affect the pattern of electrode dissolution. Chrornate can be
selectively removed from blowdown by Ion exchange with CI-.
sulfate, or hydroxide. Anlon resins will not remove trlvalent
Cr or Zn. A major advantage of ton exchange Is that no sludge
Is produced. Ion column rinse and backwash are returned to
the cool Ing tower. Chemical reductIon Is general 1y the most
economical. The major drawback of both reduction systems is
the need for sludge disposal facilities. (FT)
Descriptors: Chromium compounds; Cooling waters; Wastewater
treatment; Water reuse; Reduction; Ion exchange
Ident Iflers: blowdown
79-OO567
Chrornate handling systems for cooling tower blowdown.
Roensch. L. F.; Feltes, A. L.; Oberhofer. A. W.
Natco Chemical Co.. 29O1 Butterfleld Rd.. Oak Brook. IL
6O521
Fifth annual Industrial pollution conference Atlanta. Ga.
Apr. 19-2*. 1977
F|fth annual Industr tal pollutIon conference• Proceedings.
Edited by L. Delpino and A. Krlgman pp. 121-135 Publ.Yr-
1977
Pub): McLean. Va. Water and Wastewater Equipment
Manufacturers AssocI at ton
11lus. refs.
Abs.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
Removal of hexavalent chroinate by chemical reduc t Ion
requires the following 4 steps lower blowdown pll to 3-4 to
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DIALOG F11e41- Pollution Abstracts - 7O~B2/Apr (Copr. Cambridge Sc 1 Abs) (Item 73 of 98) User23913 23jun82
U)
H
OJ
79-OO47O
Chlorinated tyroslne in municipal waste treatment plant
products after superchlorlnatton.
Burleson, J. L. ; Peyton. <3. R. ; Glaze, W. H.
North Texas State Univ., Dept. of Chemistry and Inst. of
Applied Sciences, P.O Box 5O57. Denton. TX 762O3
BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY
19(6), 724-728. / Coden: BECTA6 Publ.Yr: June 1978
IIlus. refs.
Sum,
Languages: ENGLISH
Ooc Type: JOURNAL PAPER
1 One mil It liter of a 28-lm C12/1 aqueous solution was added
to 1 ml of a 2Q-lra/l tyroslne solution adjusted to pH *-2.
The react Ion proceeded for 3O min, and the mixture was
extracted with I ml of ether. Analysis of the extract by
GC-MS showed approximately equal proportions of mono- and
d(chlorinated phenylacetonitr He and phenylacetaldehyde;
analysis of the N-heptafluorobutyryl n-propyl ester derivative
confirmed the presence of chloro- and dlchlorotyrosIne, which
were also found In effluent from superch}orinatton facilities
in use at 3 municipal waste treatment plants. The extent to
which these and other possible chlorinated amino acids occur
In superchlorinated waste products Is not known, but is under
Investigation. (FT)
Descriptors: Municipal wastewaters; Water; Chiortnation;
Ami no ac Ids: Gas chromatography; Mass spectroscopy.;
Chior 1nated hydrocarbon compounds; Sewage treatment; Sewage
treatment plants; Effluents
IdentIflers: tyrosine; superclorination
78-O4472
Cooling water and boiler possibilities for wastewater reuse.
Morresi. A. C.; Cheremisinoff, P. N.
Hoffmann-La Roche
INWA8K
33-34,
Coden:
INDUSTRIAL WASTES 24(2),
Publ.Yr: Mar.-Apr. 1978
i1lus. no refs.
No abs.
L anguages: ENGLISH
Doc Type: JOURNAL PAPER
Cooling towers offer the most readily available source for
recyclable water. Cooling towers handling large quantities of
water (N1OO.OOO gpm) can use a variety of wastewaters as
makeup. The water conservation benefit of cooling towers must
be economically justified by balancing the reduced cost of
waste treatment against any additional treatment costs needed
to produce a reuse stream of acceptable quality, If cooling
towers are made secondary users of water. the blowdown will
contain more contaminants and require additional treatment
before discharge If water with a low dissolved solids
content is used as makeup, windage may remove enough
Impurities so that a blowdown stream is not required. If
contaminated water can be used in a cooling tower, the tower
can serve as an equalization facility to protect downstream
waste treatment from shock loads of pollutants. AM cooling
tower reuse plans must Insure that the prime function of
cooling towers-providing cool water to heat exchangers without
causing seal ing, st inttng, or corrosion problems-Is not
Impaired. Cooling tower blowdown has been used as wash water,
utility water, flare drum seal water, pump coolant, and tank
field water. If chromates are used as corrosion Inhibitors In
the cooling tower, ion exchange can recover them and make the
cool ing water acceptable for reuse. Feed water for
low-to-medium pressure boilers (N65O psf) requires softening.
deaeratlon, and silica removal. High-pressure boilers require
demtiteral ized. deaerated water. Low-pressure steam has been
generated in unflred waste heat boilers from some wastewaters.
Clean stream condensete is extensively recycled, but boiler
blowdown Is seldom used. High-pressure boiler blowdown can
sometimes be used as makeup water for low-pressure boilers (
FT)
Descriptors: Water reuse; Wastewaters; Wastewater treatment;
Waste reuse; Cooling systems; Cooling waters; Boilers
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Flle4l Pollution Abstracts - 7O-82/Apr (Copr Cambridge Sc I Abs) (Item 75 of 98) User239l3 23jun82
78-O4471
Treatment of plating wastes from the automotive Industry.
Cull Inane. M. J. , Jr.; Dietz, J- D.
Clark, Dletz and Assoc.-Engineers, Inc.
INDUSTRIAL WASTES 24(2). 29-32. Coden: INWABK
Publ.Yr: Mar.-Apr. 1978
i1lus. no refs
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Water conservation measures recommended for a Mississippi
plant Include us Ing spring-loaded shutoff nozzles on water
hoses, collecting and returning steam condensate for boiler
water makeup, using recycled water tn the buff ing process, and
using counterflow rinsing in the plating operation. Several
was tewa ter segrega 11on prac11ces were a1 so recommended. To
meet federal standards, the most cost-effectIve effluent
treatment was reduction followed by chemical precipitation.
CompIe te t rea tmen t and dIrec t d 1 scharge was more cos t
effectIve than pretreatment and discharge to the municipal
waste system. The opt imum rinse system is a modif led
countercurrent system with 5 rinse tanks, which reduced water
consumption from K40O gpm to ~J6O gpm. Features incorporated
in the treatment design include addition of an acid feeding
system for raw waste pH adjustment and use of the abandoned
oxidation pond to equalize shock loadings. The treatment
process Included the following: reduction of Cr+6 In a
continuous flow system; equalization of flow wastes; raw waste
pumping; pH adjustment in a flash mix tank; ahd coagulation
and settling in a reactor-clarifler. Provision is made for
future add! t ion of f i 1 ters and f.inal pH adjustment. Vacuum
filtration and landfill ing is the chosen method of sludge
disposal. Problems since plant startup In March (977 have
been minimal. Water consumption could be reduced a further
4O%~5O% If recycle systems and more stringent water
conservation measures were used, but these measures do not
appear to be economically justified at the present. (FT)
Descriptors; Mississippi; Automotive industry wastes; Metal
f inishing industry wastes; Chromium compounds; Water
conservat ion; Wastewa ter treatment; Wastewater treatment
plants; Industrial effluents; Reduction; Coagulation
The chemistry, environmental dtstrIbut Ion, metabolIsm,
biological effects on plants and animals, and biological
effects on man of As and As compounds are discussed In detail.
The degree of As air pollution due to smelter^ operations and
pest icIde use should decrease If currently proposed
occupatlonal and environmental standards are promulgated.
Arsenic pollution from coal burning is widely dispersed, which
minimizes its danger to public health. Common use of shale
oil would require removal of As from the oil or more careful
monitoring of As. While food supplies normally contain As.
the concentrations are very rarely harmful. Water supplies
generally contain negliglble quant 11les of As. Industr ial
effluents often contain As. but the problem is minimized by
the self-purification of receiving waters and the Improved
qualtty of wastewater discharges. Use of As pesticides was
greatly reduced wlth the Introduct ion of chlor inated
hydrocarbon and organophosphorus chemicals. With Increasing
restrlet ions on these, however, As chemicals may again be
widely used. requiring careful monitoring. Little or no
qual1 tat ive informatIon Is ava I (able regarding the fate of
arsen leaIs in the ecosphere. so ft is not possible to state
with any certainty whether As Is building up In any sector.
Individual As compounds can be determined only after isolation
by volatilization, paper chromatography, GC. or
electrophoresls. The continued concern about the association
be tween InorganIc arsenic and cancer has ra Ised ques 11one
regarding the Imp!icat tons of widespread dispersion of
inorganic arsenicals In the environment. Recommendations for
future research areas and protocols are given, (SS & FT)
Descriptors: Books; LIterature reviews; Arsenic; Arsenic
compounds; Hetaboli sm; Humans; P1 ant s; An1ma1s; F oods;
PestIcldes; SmeltIng; Chemistry; Pollutant detect 1
78-O3967
Arsenic.
Natlonal Research Councl1-Dtv . of Medical Sciences-Commlttee
on Medical and Biologic Effects of Environmental Pollutants
2 lot Constitution Ave. NW. Wash. DC 2O4I8
Medf ca1 and Biologic Effects of Env tronmentaI Po11u t ant s
332 pp Publ.Vr: 1977
Publ : Washington, D.C. National Academy of Sciences
Illus.' Indexes numerous refs. (Some in Chin.; Croatian;
Czech ; Dan.; Fr.; Ger.; Ital.; Japanese; Norw.; Pol.; Port.;
Russ. ; Span )
No abs. Price. $13 75 (pbk.)
Languages ENGLISH
Doc Type BOOK
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DIALOG Flle4l Pollution Abstracts - 7O-B2/Apr (Copr Cambridge Set Abs) (Item 77 of 98) User23913 23JunB2
UJ
M
Ul
78-O3385
Electrolysis.
Vlahakis. J.; Ouellette. R.
Electrotechnology Vol. (• Wastewater treatment and
separation methods. Edited by R. P Oueltette. J. A King and
P. N. Cheremlslnoff 193-237. Publ.Vr: 1978
Publ: Ann Arbor. Mich Ann Arbor Science Publishers
Illus. refs.
No abs.
Languages: ENGLISH
Doc Type: BOOK CHAPTER
The most Important Industrial applications of electrolysis,
a chemical process by which chemical reactions are produced
electrically In solutions or molten salts, are metal recovery
and electroextractIon, electrochemical organic synthesis, and
electroconcentratIon of solids. Among many specific potential
applications are the manufacture of propylene oxide from
propylene and water. the treatment of acid mine drainage to
recover Fe. reducing the COD of cheese whey waste, the
recovery of fatty minerals from edible fats, the regeneration
of chromated At deoxldtzers, the treatment of domestic wastes.
cyanide and organic waste treatment, and electroflotation.
Electrolytic processes produce less pollution than many
conventional techniques, and also compare favorably. on an
economic basis, with them. Electrolysis Is energy competitive
with other chemical routes for manpfacturIng chemical
compounds and, as environmental standards become more strict,
shoud become more popular In metal recovery and waste
treatment applications. (FT)
Descriptors: Electrochemistry; Reduction; Oxidation; Metals;
Wastewater treatment; Water purification; Organic wastes; Mine
drainage; Materials recovery; Chemical wastes; Waste treatment
; Technology
Identifiers: electrolysis
78-O333O
Aluminum manufacturer removes chromium.
Anonymous
INDUSTRIAL WASTES 24(1), 24, 34. Coden: INWABK
Publ.Vr: Jan.-Feb. 1978
11lus. no refs.
No abs.
Languages ENGLISH
Doc Type: JOURNAL PAPER
A New Hampshire aluminum company Installed a Hussong/Couplan
Chrome Removal Treatment System to treat Its raw effluent.
The effluent contains 164 mg/1 total Cr. 136 mg/1 hexavalent
Cr. 62O mg/1 total P. and 22.8 mg/1 Al. The decision was
Dased on 2 factors. The system reduced the pollutants to the
lowest concentrations In the final effluent and met, by a
comfortable margin, the requirements of the final EPA
regulations and the local municipal sewer code. Another
Hussong/Couplan System employing sphagnum peat as the
treatment medium can readily be tied Into the existing system.
In a series flow arrangement, at a later date. Changing
conditions can be met without costly, extensive replacement or
modification of the present system. The Hussong/Couplan
System treats the wastewaters with ferric chloride (FeC13) and
sodium sulfide (Na2S) at a pH In the 5-7 range In such a way
as to obtain a specific molar ratio of Cr6+6. FeCI3, and Na2S
In the effluent. A massive precipitate Is formed which
carried down virtually all of the Cr, both hexavalent and
trtvalent. The system at the Al plant Is a 6.OOO gpd system
and Is composed of 3 holding-batch tanks, chemical adders.
misers, controls, and sensors. To Insure the continuing
purity of the discharge, colorlmetrlc checks are made at the
precipitation tank. (FT)
Descriptors: Chromium; Aluminum; Metal Industry wastes;
Effluent treatment; Industrial effluents; Precipitation;
Contaminant removal
Identifiers. Hussong/Couplan Treatment System
78-O332O
Organochlorlnated residues In wastewaters before and after
treatment.
Martin. G. B.; Gosselln, C.
Unlverslte Laval, Centre de Recherches en Nutrition, Oue
GIK 7P4, Can.
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH-PART A AI3(I).
1-11, Coden: JESEDU Publ.Yr: 1978
Illus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
PCBs and pesticides were measured In effluent from the
primary treatment sand deposition stage and from the secondary
oxidation basin stage of the treatment plant of a small
Quebecois town. During a 24-hr sampling period, the secondary
treatment reduced TOE concentrations from a mean of O.O8 ppb
to a mean of O.O3 ppb; DDT concentrations were so close to the
detection limit that no conclusions can be drawn. PCBs were
reduced from 1.29 to O.38 ppb. Over a 5-d sampling period,
PCB concentrations were O.5O-2.OO ppb before secondary
treatment and O.02-O.6O ppb after It. The pattern of PCB
chromatograms was affected by the treatment, with an Increase
in the proportion of the less chlorinated PCBs evident. (FT)
Descriptors: PCB compounds; Pesticides; DDT; Organochlorine
compounds; Wastewater treatment
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DIALOG F11e41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Sci Abs) (Item 8O of 98) User-23913 23junB2
U)
78-O3235
The distribution of heavy metals In anaerobic digestion.
Hayes, T. D. ; The is, T. I.
Cornel 1 Univ., Dept. of Agr fculturat Engineer ing, Ithaca. NY
H850
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5O(I). 61-72,
Coden: JWPFA5 Publ.Yr: Jan. (978
1 Ilus. refs.
Eng., Fr., Ger,, Port., Span. abs.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
Bench scale anaerobic digesters using municipal wastewater
sludge were dosed with different levels of heavy metals (Cr+3.
Cr + 6, Cd, Cu+2. Ml , Pb. and Zn) to determine thetr
distrIbutIon and note their effects under operating
conditions Dos ings were made In both a stepwlse and pulse
manner. Characteristic responses observed during periods of
digester distress Included Increased volatile acids and total
organic carbon, decreased gas product Ion and methane
compos 11Ion, and depressed values of pH. The order of
toxiclty established 1n this study was NIK CuKPbKCr+6JCr+4KZn.
Toxic limits for Cd were not reached. Metals were rapidly
removed from digester supernatant in excess of 95%. The total
Insoluble portion was divided between Inorganic precipitates
and the blomass fraction. Between 3Q% and 6O% of the metals
were associated with the bacterlal eel Is. Tox1c effects
became apparent at or near the maximum metals taken up by the
digester component. (AM)
DescrIptors: Anaerobic process; Sludge digest Ion;
Distribution; Chromium; Copper; Cadmium; Nickel; Lead; Zinc;
MunlcIpal wastewatens; Pollutant removal; Heavy metals
proton activity In the solut ion and was & max Imum at a moJe
rat la of protons:Cr+6 of 1 O. DesorptIon studies were
performed at d1fferent pH values w1th various ac ids and sod turn
hydroxide (NaOH). Alkaline desorptlon was more effective than
the acid desorption. The Cr+6 was desorbed In the alkaline pH
regions, whereas Cr+3 was the prevailing species in the case
of acid desorptlon. Using NaOH, K8O% Cr was desorbed at a pi I
value close to 14. At a Cr+6 concentration higher than the
Initial proton concentration, an amount equal to the initial
amount of protons Is first adsorbed, with any rema inlng
removal of Cr being by hydro!yt ic adsorpt ion. At a
concentrat Ion lower than the Initial proton concentrat ton,
reduction of Cr+6 to Cr+3 takes place, with reduced Cr+3
remaining in solution at low pH values. The degree of
reduction is a function of the proton:Cr+6 ratio, the initial
pH value, and the amount of activated carbon In solution. The
final form of adsorbed Cr within the activated carbon is in
the hexavalent form. An activated carbon column configuration
produced significant Cr+6 removal when the proton:Cr+6 ratio
1s 1.0. (FT)
Descriptors; Activated carbon; Adsorption; Chromium;
Contaminant removal; Wastewater treatment
78-O2754
Chromium removal with activated carbon.
Kim, J. I.; Zoltek, J., Jr.
Unlv of Flor Ida, Dept. of Environmental Engineer Ing
Sciences. Gainesville, FL 32611
Eighth International conference on water pollution research
Sydney. Australia Oct. 17-22, 1976
Eighth International conference on water pollution research.
Edited by S. H Jenkins. In PROGRESS IN WATER TECHNOLOGY 9(1)
143-155, Coden: PGWTA2 Publ.Vr; 1977
i1lus. refs.
No abs.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
Mechanisms responsible for Cr adsorption and reduction by
activated carbon are described and results are presented to
help in the development of a process for Cr+6 removal. The
activated carbon used was Flltrasorb 4OO and the Cr levels
were determined by AAS. A solution of Cr+6 in the presence of
activated carbon was reduced to Cr+3 to a greater extent as
the pH was Increased. Total Cr adsorption Increased to a
maximum with Increasing pH up to an Initial Cr+6 concentration
of 3OOM, after which the adsorption decreased. The total
amount of Cr adsorbed was a direct funct ton of tho initial
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DIALOG F1le41' Pollution Abstracts - 7O~82/Apr (Copr Cambridge Scl Abs) (Item 82 of 98) User239l3 23Jun82
reverse osmosIs and
UJ
7S-O257O
Present art and status of
ultrafIItratlon In Japan.
Ohya. H.
Yokohama National Univ.. Dept. of Chemical Engineering.
V ok ohama, Japa n
International Congress on Desalination Tokyo, Japan Nov.
27-Dec. 3. 1977
Proceedings of the Internet ional Congress on OesalinatIon
and Water Reuse: Vols. I and 2. In DESALINATION 22(1-3).
223-233, Coden: OSLNAH Publ.Yr; Dec. 1977
lllus no refs.
Sum.
Languages: ENGLISH
Ooc Type: CONFERENCE PAPER
.Japan will have a water supply deficit of 70 billion TPY by
1985. The deficit can be made up by desalination and by
multiple reuse of process water. RO seems most economical for
water reuse applications. In a typical system, the wastewater
Is divided Into a low salinity stream treated by conventional
tertiary treatment systems and a high-salinity system treated
by RO. Flow charts for systems processing Ion exchange
regenerating reagent, soybean fermentation wastes, and bean
paste wastes are presented. Manufacturers, distrIbutors,
licensees and sublicensees of RO and ultraf11tratIon systems
In Japan are listed. The capacities of RO units distributed
by Japanese companies are 1tsted. Typical operattonal data
are given for a new type of cellulose acetate, hollow fine
fiber module designed to minimize fouling deposits on membrane
surfaces (Hoilosep). A tubular module using plast ic
reinforced porous fiberglass tubes as support Is described. A
new polyheterocycl1c pol y benz ttnldazo lone membrane which can
wlthstand strong acid has shown promise In concentrating
chromic acid rinses. (FT)
DescrIptors: Japan; Reverse osmosis; F11tratIon; Membranes;
Wastewater treatment; Food processing Industry wastes;
Industrlal effluents; OesalinatIon; Technology
Identifiers- ultraf11tration
coagulation-sedimentat ton for both r tnslng water and used
bath. Such treatment does not satIsfy recent municipal
regulations. A new process treats rinse water, containing the
bulk of cyanide and Cr wastes, with Ion exchangers; acid or
aIkalIne wastewater Is treated by chelate res in af ter
coagulation-sedimentation. The treated water can be returned
to the shop. The mixed bed exchanger consists of a strongly
acid and a weakly basic an Ion exchange resin after an
activated carbon filter, followed by a strongly basic an Ion
exchanger. At the near neutral pH value of the wastewater
made possible by this system, complex cyanides are not
precipitated nor cyanide gas produced; free cyanide which
passes the mixed bed exchanger Is caught by the strongly basic
exchanger. Regenerat ton water and deter lorated bath are
treated with sodium hypochlorlte and ferric sulfate. Chromium
(III) Is treated with other cations with a strongly acid
exchange resin; hydrogen chromate and chromate Ion are treated
with other antons by weakly basic exchange resins. Wastewater
containing heavy metals other than cyanide and Cr Is treated
by coagulation and sedimentation, sand filtration, and chelate
resins which adsorb the metals selectively In series. (FT)
Descriptors: Wastewater treatment; Cyanides; Metal fInlshlng
1ndustry wastes; Chrom1urn; Heavy metaIs; Ion exchange;
Industrial effluents; Resins
78-O256O
An experience on re-use of waste water discharged from
plating shop.
Mural. Y.; Yamadera. T.; Koike. Y-
Hitachi Plant Engineering ft Construction Co., Water & Waste
Water Treatment Otv.. Tokyo, Japan
InternatIonal Congress on DesalInatIon Tokyo, Japan Nov.
27-Dec. 3, 1977
Proceedings of the International
and Water Reuse: Vols. 1 and 2
97-IO4, Coden: OSLNAH Publ.Yr
IIlus. refs.
No abs.
Languages: ENGLISH
Doc Type' CONFERENCE PAPER
Convent ional treatment processes for metal plat ing
was tewaters cons 1st of ox IdatIon, reductloo. and
etal
Congress on Desal(nation
In DESALINATION 22(1-3),
Dec. 1977
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DIALOG Flle4l: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 84 of 98) User239l3 23jun82
3196
U>
(-•
CO
78-O2556
An Integrated Industrial waste water treatment system using
electroflotatlon and reverse osmosis.
Roth, H. P.; Ferguson, p. V.
Swissair Engineering, Metals Technology Section. Zurich.
Switz
International Congress on Desalination Tokyo, Japan Nov
27-Dec. 3. 1977
Proceedings of the International Congress on Desalination
and Water Reuse. Vols. I and 2. In DESALINATION 22(1-3),
49-63. Coden: OSLNAH Publ.Vr: Dec. 1977
Illus. refs.
Sum
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
At the Swissair Maintenance and Overhaul Base In Zurich,
wastewater and process effluent treatment Is centralized
except 'for cyanides and chromate plating wastes
detoxification. The central treatment for wastewater consists
of clarification stages, neutralization, and sludge treatment
performed by electroflotatIon. Process water treatment,
consisting of a desalination stage. Is performed by RO,
Including necessary pro- and post treatment equipment. In the
electroflotatlon process, electrolytleally produced minute gas
bubbles which adhere to flocculatfon particles are used to
separate clarified water from the sludge phase. Batch
treatment times are 2O-3O mln. The sludge layer which forms
on top of the tank Is sklmrned pneumatically at regular
intervals. In this facility. electroflotatIon Is laid out In
2 Independent lines with a capacity of 2O m3/hr each. The
outlet stream contains J5 ppm SS. Intermediate treatment
consisting of post-alum flocculatlon followed by multimedia
pressure filtration, and pH and scale Inhibitor conditioning
prepares the stream for RO. Modified cellulose acetate spiral
module membranes are used. Design recovery rate Is 8O54 on a
capacity of 72O m3/d. Automatic flushing devices control
membrane fouling. Average salt rejection rates are 98 4%.
Dally plant utilization Is 16 hr-13 hr for waste and 3 hr for
city water. The city water stream has a beneficial effect on
membrane flux performance restoration; the bank flushing
system needs to be used only every 4 wk. Permeate
posttreatment Includes degas IfIcatIon, pH adjustment, and
carbon bed filtration. Operational costs of the facility are
calculated at about $I.92/I.OOO gal. (FT)
Descriptors Switzerland; Wastewater treatment; Reverse
osmosis; Flotation; Desalination; Industrial effluents;
Neutralization; Sludge treatment
Identifiers- electroflotatIon; Swissair; Zurich
Uppsala, Sweden
WATER RESEARCH
1977
11(9), 8OI-8O5.
refs. (Some In Scan.)
Coden- WATRAG
Publ.Yr:
Illus.
Abs.
Languages: ENGLISH
Doc Type- JOURNAL PAPER
In order to fulfill the objective of a water control program
based on frequent sampling In several wastewater treatment
plants, rivers. and lakes, a simplified method for measuring
COD was developed. • The procedure. called the RR method.
Includes small sample and reagent volume, rapid addition of a
mixture of all reagents to the sample, exclusion of mercury,
and autoclavlng at !2OdegC for 1 hr In flasks with fitted
glass stoppers. To avoid dilution before analysis, the method
was adapted for wastewater (IO-3OO mg/1 O2) and fresh water
(IO-IOO mg/1 O2). Parallel analyses on different types of
water samples according to standard methods showed that the
yield by the RR method was about 1O% lower. With water from
the wastewater treatment plant at Uppsala (COD around 2O mg/1
02), the two methods gave an identical result. The somewhat
lower yield was mostly due to decreased dlchromate
concentration and oxidation temperature The lower oxidation
potential made correction for chloride Interference
unnecessary below I g/l CI-. The RR method also showed a good
correlation to the values for potassium permanganate-consumpt-
ion. Parallel analyses of 318 samples from 14
wastewater-receivlng lakes gave the correlation coefficient
r-+0.90. (AM)
Descriptors: COD; Acids; Chromium compounds; Water sampling;
Sweden; Wastewater treatment plants; Lakes; Rivers; Measuring
methods
Identifiers: acld-dlchromate; autoclavlng; Uppsala; RR
method
78-OI295
A mercury-free accelerated method for determining the
chemical oxygen demand of large numbers of water samples by
autoclavlng them under pressure with acld-dlchromate.
Rydlng. S. -O.; Forsberg, A.
National Swedish Environment Protect Ion Board, Inst. of
Physiological Botany. Algal Assay Lab., Box 54O, S-751 21
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DIALOG Fi!e41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 86 of 98) Usei-23913 23)un82
CO
H
78-O1288
Advanced treatment methods for electroplating wastes.
Jakobsen. K.; Laska, R.
EPA, Office of Energy. Minerals, and Industry. 4OI M St. SW,
Wash.. DC 2O46O
9(tO),
42-46.
Coden: PLENBW
POLLUTION ENGINEERING
Publ.Vr: Oct. 1977
11lus. no refs.
Sum.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
The EPA withdrew Its metal finishing Industry effluent
guidelines because they appeared potentially destructive to
the economic viability of the Industry. The EPA Is sponsoring
projects to help electroplaters achieve control of effluents
economically and effectively. Ion exchange and reverse
osmosis show the most technical and economical promise of the
several control technologies under development, but each
technology wilt optimally apply to specific wastewater
streams. Pilot and full scale demonstrations showed that
chromate solution recovered by Ion exchange can be recycled
Into product manufacture without sacrificing product quality.
The chromate composition of a demonstration plant effluent Is
being reduced from 2.7OO ppm to 1-2 ppm. The treatment system
was designed to treat 6O gpm of Influent and discharge an
effluent which Is within statutory limits for pH and heavy
metal content. A demonstration combined reverse osmosis with
solar evaporation for disposal of removed contaminants and
achieved zero discharge to navigable waters. Water
consumption was cut by 75O.OOO gal/mo. (FT)
Descriptors: Federal agencies; Federal regulations;
Wastewater treatment; Metal finishing Industry waste's; Reverse
osmosis; Ion exchange
Identifiers: EPA
78-OO417
Rate . of mlcroblal transformation of polycycllc aromatic
hydrocarbons: A chromatographIc quantification procedure.
Herbes. S. f.. ; Schwal I, I. R. ; Williams, G. A.
Oak Ridge National Lab., Environmental Science Dlv.. Oak
Ridge. TN 37B3O
APPLIED AND ENVIRONMENTAL MICROBIOLOGY 34(2), 244-246,
Coden: AEMIDF Publ Yr: Aug. 1977
tllus. refs.
Abs.
Languages ENGLISH
A chromatographtc procedure was developed for Isolating and
quantifying mlcroblal transformation products of qtC-laba'led
polycycllc aromatic hydrocarbons. PAH-ut111zing cultures were
Isolated From an oil-drilling site and a wastewater treatment
unit. Microorganisms were grown by Inoculation of soil and
wastewater samples Into autoclaved basal Inorganic medium
saturated with naphthalene or phenanthrene; several bacterial
strains were Isolated. PAH transformation rates were
determined by centrifuglng cells from an exponential culture,
washing them, and suspending them In a hydrocarbon-free basal
medium. A qtC-labeled PAH compound was added in 4 II of
acetone, and the culture Incubated at 23.C for 2-3 d.
Extracts were combined and evaporated to near dryness. and the
residue redlssolved In benzene. Transformation rates of
naphthalene, anthracene. benz(a)anthracene, and benz(a)pyrene
by a mixed bacterial population were measured. With this
procedure, extremely slow or Incomplete transformations may be
quantified that would not be detectable by previously used
techniques. (AA & from Text)
Descriptors: Aromatic compounds; Hydrocarbons; Cyclic
compounds; Bacteria; Chromatography; Effluents: Carcinogens;
Water pollutants; Microorganisms
Identifiers: PAH
77-05373
Removing soluble metals from wastewater.
METZNER. A.V.
Ecodyne Corp., Industrial Waste Treatment Dlv.
Water & Sewage Works. 124(4): 98-1O1. Apr. 1977 Publ.Yr:
1977
Languages: ENGLISH
Descriptors: ZINC; CHROMIUM; WASTEWATER TREATMENT: COPPER;
TECHNOLOGY; IRON; NICKEL
Identifiers: METAL REMOVAL; CYANIDES
77-O524O
The sulfex heavy metal waste treatment process.
FEIGENBAUM. H.N.
Permutlt Co.. E. 49 Midland Ave.. Paramus. NJ O7652
Proceedings of the Fifth Annual Industrial
PolluttonConference. Edited By L. Delplno and A. Krtgman.
Mclean.Va.: Water and Wastewater Equipment ManufacturersAssoc-
latlon. 1977. 629-642 Publ.Yr: 1977
Languages: ENGLISH
Descriptors: IRON; COOLING WATERS; CHROMIUM COMPOUNDS; METAL
FINISHING INDUSTRY WASTES; SULFUR COMPOUNDS; CHROMIUM; HEAVY
METALS; WASTEWATER TREATMENT
Identifiers: SULFEX: PERMUT1T COMPANY
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DIALOG File.11. Pollution Abstracts 7O-82/Apr (Copr Cambridge Scl Abs) (Item 9O of 98) Usor23913 23jun82
77-O521S
Chromate handling systems for cooling tower blowdown.
ROENSCH, L.F.
Nalco Chemical Co.. 29O1 Butterfield Rd., Oak Brook. 1L6OS21
Proceedings of the Fifth Annual Industrial
Pol Hit ionConf erence. Edited By L., Delptno and A. Krlgman.
Mclean.Va.: Water and Wastewater Equipment ManufacturersAssoc-
iation, 1977. pp. 121-135 Publ.Yr: 1977
Languages: ENGLISH
Descriptors: COOLING WATERS; ECONOMICS; ION EXCHANGE;
WASTEWATER TREATMENT; CHROMIUM COMPOUNDS
74-O2237
Petroleum hydrocarbons and fatty acids in Wastewater
effluents.
QUINN, J.G.
WHOI, Main St., Woods Hole, MA 02543
Water Pollution Control Federation. Journal. 45(1) 7O4-712.
Apr. 1973 Publ.Vr: 1973
Languages: ENGLISH
Descriptors: CHROMATOGRAPHY; EFFLUENTS; HYDROCARBONS; LIP1DS
; PETROLEUM; WASTE WATER TREATMENT PLANTS
Identifiers: FATTY ACIDS
77-OO4O7
• Waste treatment for a metal finishing plant.
YOUNG. R.A.
'Pollution Engineering, 1301 S. Grove Ave., Barrlngton,
IL6OOIO
Pollution Engineering. 8(9): 4O-41. Sept. 1976 Publ.Yr:
1976
Languages: ENGLISH
Descriptors: MARYLAND; WATER QUALITY; ENGINEERING; METAL
FINISHING INDUSTRY WASTES; CHROMIUM; WASTEWATER TREATMENT
Identifiers. GENERAL ELECTRIC CO.
76-O5299
(jj Pollution abatement through the treatment of Industrial
to waste water with Ion exchange resins.
O WAITZ, W.H.. JR.
Rohm and Haas Co.. i Pollution Control Research Dept..
SOOORichraond St., Philadelphia. PA 19137
Institute of Environmental Sciences: 22nd AnnuatTechnlcal
Meeting. Mt. Prospect, 111 : Institute ofEnvironmental
Sciences. 1976. pp. 491-495 Publ.Yr: 1976
Languages: ENGLISH
Descriptors: WASTEWATER TREATMENT; RESINS; ECONOMICS;
CYANIDES; METALS; BORON; ION EXCHANGE; INDUSTRIAL EFFLUENTS
Identifiers: CHROMATFS
72-O6467 72-5TF-OO98I
Contlnous effluent analysis halts chromate batch tests.
ANONYMOUS,
UNKNOWN
Chemical Processing. Chicago, 34(12): 9, Mld-Nov. 19
Publ.Yr- 1971
Languages: ENGLISH
Descriptors: COLORIMETRY; WASTEWATER TREATMENT; CHROMATES
Identifiers: TURBIDIMETERS
72-O1025 72-1TF-OO228
Chromate pollution of watei—detection, effects, and
prevention: A bibliography.
STEMPLE. RUTH
AEC, Oak Ridge National Lab.. V-12 Technical Library. TN
U. S. Atomic Energy Commission. Oak Ridge
Nat tonal Laboratory. Oak Ridge. Tenn. Report No. ORNL TM-345O.
20pages. Oct 1971 Publ.Yr; 1971
Languages: ENGLISH
Descriptors: INDUSTRIAL WASTES; WATER POLLUTANTS; WASTEWATER
TREATMENT; CHROMATES
Identifiers: BIBLIOGRAPHY
74-O3343
Gas-liquid chromatographtc separation of sulfur from
chlorinated pesticide residues in wastewater samples.
KUO. C.L.
County Sanitation Districts of Los Angeles County, 21O1S.
Workman Mill Ln.. Whlttler. CA 906O1
Bulletin of Environmental Contamination andToxIcology. 9(2).
1O8-II5. Feb 1973 Publ.Yr: 1973
Languages- ENGLISH
Descriptors: CHLORINE; CHROMATOGRAPHY; HALOGENATEO
PESTICIDES; MEASURING METHODS; PESTICIDE RESIDUES; SULFUR
REMOVAL; WASTE WATERS
Identifiers GLC
-------
DIALOG Ft)e4l Pollution Abstracts - 7O-B2/Apr (Copr Cambridge Set Abs) (Item 97 of 98) Usei-23913 23jun82
7I-O4278 71-3Tf-OO4O7
Uptake of nitrosyl 106-ruthenlum on chit In and chltosan from
waste solutions and polluted sea-water.
MUZZARELLI, RICCARDO A. A.
Univ. of Bologna, Clamtclan Chemical Inst., It.
Water Research. New York. 4(6): 451-455. June 197O
Publ.Vr: 197O
Languages: ENGLISH
Descriptors: POLYMERS; CHROMATOGRAPHY; RADIOACTIVE WASTES;
CHELATION; WASTEWATER TREATMENT
Identifiers- RADIONUCLIDE UPTAKE
71-O2852 7I-2TF-OO342
Rid sewage of toxic Inorganics.
FULMER. MARY
Columbus. OH
Water and Wastes Engineering. New York, 8(l>. 26-27,Jan.
1971 Publ.Yr: 1971
Languages: ENGLISH
Descriptors: CHROMIUM; INDUSTRIAL WASTES; ION EXCHANGE;
WASTEWATER TREATMENT; SEWAGE
OJ
fo
-------
Print 4/5/1-6)
DIALOG F11e41: Pollution Abstract's - 7O-82/Apr
(Copr. Cambridge ScI Abs) (Item 1 or 61) User 239 K) 23jun82
32OO
U)
to
NJ
Priority Pollutants In Large Municipal Treatment
19SO
PP-
144-150,
82-O2O74
Fate of
Plants
Lue-HIng, C.j Lord!, D.T.; Kelada, N.P.
Metro. Sanitary Olst. Greater Chicago, IL
AIChE Nat. Mtg. Boston. Portland. Chicago
IN "WATER - 198O VOL. 77, NO. 209.
Publ.Yr: t9Bt
AICHE. 345 EAST 47 ST., NEW YORK, NY 1OO17
SUMMARY LANGUAGE - ENGLISH
Languages: ENGLISH
The U.S. Environmental Protection Agency has Issued a list
of 129 priority pollutants which Include metals, cyanides,
phenols. pesticides and other organtcs. The Metropolitan
Sanitary District of Greater Chicago (MSOGC) which operates
seven treatment plants has regulated heavy metals, phenols and
cyanides for a number of years. The heavy metals found In the
Influents Include chromium, copper, zinc. Iron, nickel, and
cadmium. Substantial but variable removals do occur with the
effluents reaching some background level for a specific metal.
These metals are found to concentrate In the treatment plant
sludges- The results of a screening of the occurrence of the
priority organlcs at four of the MSDGC treatment plants showed
relatively few organlcs occurring In detectable quantities.
The concentrations of those found were highly variable but
generally less than 1OO mu g/1 In the influents and less than
2O mu g/1 In the effuents.
Descriptors: pollutants; organic compounds; heavy metals;
effluents; wastewater treatment plants; sludge; cyanides:
phenol; pesticides; contamination ^
B2-OO55O
Method and Apparatus for Removing Biodegradable Compounds
Frcm Wastewater
Bhattacharyya, A.
Republic Steel Corp.
Buffalo, NY
U.S. PAT. OFF. GAZ
1981
Pat. No. 4.271.O13
Languages: ENGLISH-
A method for removing biodegradable compounds selected from
the group which Include oils, volatile organlcs. phenol Ics
free and fixed ammonia compounds, thlosulfates, thlocyanates.
cyanides, sulffdes and the like from a feed wastewater:
distilling said wastewater to remove said free ammonia
compounds, oils and volatile organlcs.
Descriptors: BlodegradatIon: Ammonia compounds; Cyanides;
Wastewater treatment; Patent; Instruments; Pollution control
equipment
Cleveland,
VOL. 1O07, NO.
OH Hanna Furnace Corp..
1. p. 274, Publ.Yr:
Kult. W.J.M.; Babcock, A.R.
Cominco Ltd., Vancouver, Can
U. S. PAT. OFF. GAZ. VOL. IOO3. NO. 2 . p. 7O3 ,
Publ.Yr: 1981
Pat. No. 4.25O.03O
Languages: ENGLISH
A method for the removal of dissolved free and complex
cyanides from water-containing effluent which comprises
controlling the pH of said effuent In a range of about 7.O to
8.5 and contacting said effuent with an effective amount of an
Insoluble solid Iron sulflde chosen from at least one of
ferrous sulflde and ferric sulflde having particle sizes
smaller than about 3QO mu for a period of at least about 5
minutes to remove said dissolved free and complex cyanides to
a desired level, said effective amount being sufficient to
give a weight ratio of said Iron sulflde to total cyanide tn
said effluent of greater than about 2:1.
Descriptors: Cyanides; Effluents; Wastewaters; pit;
Wastewater treatment; Water purification
81-O388O
Response of Methane Fermentation to Cyanide and Chloroform
Vang, J.; Speece. R.E.; Parkin. G.F.; Kocher, W.; Gossett.
J.
Drexel Univ.. Phi la., PA
Tenth Int. Conf. IAWPR Toronto, Ont. Jun. 23-27, 198O
WATER SCI. & TECH. VOL. 13. NO. 2 . Publ.Yr: 1981
Languages: ENGLISH
The anaerobic digestion process has excellent potential for
the treatment of warm Industrial wastewaters. However this
process is generally considered to be especially sensitive to
many toxicants which occur occasionally or chronically In
Industrial wastewaters. Cyanide and chloroform were selected
as sample toxicants which show Inhibition of methane
production at concentrations less than 1 mg/1. This study was
directed toward an evaluation of the inhibition pattern of
these two toxicants. The effect of toxicant concentration on
methane production recovery pattern was determined. Suspended
growth systems were to study toxlclty acclimation
characteristics and recovery patterns.
Descriptors: Industrial effluents; Toxicants; Cyanides;
Methane; Anaerobic digestion; Chloroform
B1-O395I
Process for the Removal of Cyanides From Effluent
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DIALOG rilell Pollution Abstracts - 7O-82/Apr (Copr. Cambridge SO Abs) (Item
5 of 61) User-23913 23Jun82
8I-O38I9
lon-Precipltate Flotation of Iron-Cyanide Complexes
Bucsh, R.O ; Spottlswood, D.J.; Lower, O.W.
Int. Nickel Inc . SterlIng Forest. N.Y.
U. WATER POLLUT. CONTR. FED, VOL. 52, NO. 12 . pp.
2925-293O . Publ.Yr: 198O
Languages: ENGLISH
An ion-precipitate flotation process Is proposed to remove
Iron-cyanide complexes from wastewaters. A quarternary amlne,
trlcaprylmethyl ammonium chloride, Is used to precipitate the
Iron-cyanide complexes as a waxy solid, a material that Is
floated Both cyanide and ferrocyanlde removal are Included,
but the emphasis of this work Is on ferrlcyanlde removal. The
variables studied were: surfactant dosage, the presence of
chloride Ion, solution flow ra'te. airflow rate. Initial
ferrlcyanlde concentration, and the pH of the feed.
Descriptors. Ions; Flotation; Wastewaters; Solids; Flow
rates; Chemical compounds; Iron compounds
Identifiers: Iron-cyanide
81-OI797
Foam flotation treatment of Industrial wastewaters:
Laboratory and pilot scale.
Wilson. D. J.; Thackston. E L.
Vanderbllt Univ., Nashville. TN 37235
U S- Environmental Protection Agency. Office of Research and
Development. Environmental Protection Technology Series
Coden EPTSBT Publ.Yr: Jun I98O
M lus. 9O refs.
Abs. (Available from NTIS. Springfield, VA 22161)
Languages: ENGLISH
TREATMENT CODES: D .(DESCRIPTIVE) ; I .(INVESTIGATIVE/OBSER-
VATION)
A floe foam flotation pilot plant removed Pb and Zn In •
dilute aqueous solution to quite low concentrations. Design
Improvements are presented. The floe foam flotation of Zn Is
'readily carried out with aluminum hydroxide (A1(OH)3) and
sodium lauryl sulfate (NLS). Chromium hydroxide Is floated
with NLS. but adsorbing colloid flotation of Crt3 with ferric
hydroxide (Fe(OH)3) or AI(OH)3 yielded better results. Cobalt
and N1 levels are reduced to =1 mg/L by flotation with AI(OH)3
and NLS. The Mn+2 levels can be reduced to 1-2 mg/L by
flotation with Fe(OH)3 and NLS. Floe foam flotation of Cu was
compatible with several precipitation prelreatments (soda ash,
lime. Fe(OII)3, arid AI (OH)3 >. although modifications were
needed to prevent interference from excessive Ca or CO3-2.
Therefore, floe foam flotation can be used as a polishing
treatment. The flotation of mixtures of Cu+2, Pb+2, and Zn*2
was conducted using Fe(OH)3 and NLS. The flotation of simple
and complexed cyanides and mixtures of metal cyanide complexes
was also conducted with Fe(OH)3 and NLS; .a pH of "5 Is
optimum. A surface adsorption model for floe foam flotation
was analyzed and accounted for the effects of surfactant
concentration, ionic strength, specifically Adsorbed Ions, and
surfactant hydrocarbon chain length. (AM)
Descriptors- Flotation; Industrial wastes: Wastewater
treatment; Pilot plants: Engineering; Flocculation: Ions;
Surfactants; Iron compounds; Aluminum compounds; Heavy metals;
Zinc; Nickel; Manganese; Chromium; Cobalt; Copper; Lead;
Chemical treatment; Adsorption
Identifiers: floe foam flotation
81-01743
Mechanism and kinetics of cyanide ozonatlon In water.
Zeevalkink, iS. A.; Vlsser, D. C.; Arnoldy, P.; Boelhouwer,
c.
Univ. of Amsterdam, Lab. of Chemical Tech.. Plantage
Muldergracht 3O. Amsterdam, Holland
Water Research 14(lo), 1375 1385, Coden: WATRAG
Publ.Yr: I98O
11lus. refs.
Abs.
Languages: ENGLISH
Doc Type-. JOURNAL PAPER
TREATMENT CODES: T .(THEORETICAL/MATHEMATICAL) ; D
.(DESCRIPTIVE) ; I .(INVESTIGATIVE/OBSERVATION)
The rate of oxidation by 03 of potassium cyanide into
cyanate was measured In alkaline aqueous solutions buffered at
a pH of II.a and a temperature of 2OdegC. The Initial cyanide
concentration was usually 1OO g/m3. Under these conditions,
the reaction rate can, within the experimental error, be
described by an equation which is of first order in O3 and
Independent of the cyanide concentration. The reaction rate
Is so large that the conversion Is limited by mass transfer.
Mass balances show that 1 mole of O3 oxidizes 1 mole of
cyanide. The oxidation of cyanide Is part of a reaction
sequence similar to the O3 decomposition mechanism. For both
react ions-cyanide oxidation and O3 decay-mechanisms are
proposed. The kinetics predicted for the O3 decay are In
agreement with experimental data. The mechanism proposed for
the cyanide oxidation predicts a reaction rate equation which
has been supported by experimental evidence. (AM)
Descriptors: Kinetics; Ozonatlon; Mathematical analysis;
Wastewater treatment; Nitrogen compounds; Chemical treatment;
Metal finishing Industry wastes; Chemical reactions;
Engineer Ing
Identifiers: cyanide ozonatlon
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DIALOG rile4l Pollution Abstracts - 7O 82/Apr (Copr. Cambridge Scl Abs) (Item a of 61) Usei-23913 23Jun82
U)
K)
81-OO537
Automatic water quality analyzers for wastewater collection
and treatment
Murakami, K.
Ministry of Construction. Public Works Research Inst.. Water
Quality Section, Toyosato-cho, Tsukuba-gun. Ibarakl-ken, Japan
WATER POLLUTION CONTROL FEDERATION. JOURNAL 52(5).
938-942, Coden JWPFA5 Publ.Yr: May 198O
no refs.
Eng., Fr.,
Languages:
Ger., Port., Span. abs.
ENGLISH
Doc Type: JOURNAL PAPER
The current status of automatic water quality analyzers and
sensors for wastewater collection and treatment systems In
Japan Is described. If automatic analyzers for cyanide, Cr,
Cd. and measurement and recording of organic loading
discharged from wastewater treatment plants are to be
Implemented In Japan, automatic analyzers for organic
substances will have to be used widely. The performance of
automatic analyzers and sensors for treatment process controls
was evaluated at various locations. (AM)
Descriptors. Heavy metals; Toxic materials; Water quality;
Monitoring Instruments; Wastewater treatment; Japan
Identifiers: automatic analyzers and sensors'
BI-OO522
Inhibitory effects on nitrification by typical compounds In
coke plant wastewaters.
Ramadorl. R.; Beccarl, M.; Passlno, R.; Tandol, V.
IRSA-CNR. Via Reno 1-OO198 Rome. Italy
ENVIRONMENTAL TECHNOLOGY LETTERS 1(5). 245-252.
Publ.Yr: May 198O
1 Ilus 16 refs.
Abs.
Languages- ENGLISH
Doc Type: JOURNAL PAPER
Nitrifying sludge for the nitrification kinetic studies was
obtained from a steady state laboratory biological plant,
mixed with a synthetic NH3 substrate to a predetermined
concentration, and then Introduced Into a batch reactor. The
kinetics were monitored by determining the amount of alkail
used up In neutralizing the acidity produced during oxidation
of NH3 to NO2-. The method Is automated and gives more
accurate results than those obtained with respIrometrIc
methods. Aniline. qulnollne, pyrldlne and sulfides are
significant Inhibitors. (FT)
Descriptors. Nitrification; Coke; Industrial effluents
Wastewaters; Biological treatment; Aromatic compounds
Chemical reactions: Nitrogen compounds; Sulfur compounds
Mathematical analysis; Laboratory methods; Thermodynamics
Kinetics; Bacteria
Identifiers: nitrification Inhibition; coke plan
wastewaters: 6 Inhibitor types; aniline; qulnollne; cyanides
phenols; pyrldlne; methylpyrIdlne; sulfides; thiocyanates
Ni trosomas
8I-OO5O8
Evaluation of reverse osmosis membranes for treatment of
electroplating rlnsewater.
McNulty, K J.; Hoover. P. R.
Abcor, inc., Walden Div., Wilmington, MA O1887
U.S. ENVIRONMENTAL PROTECTION AGENCY. OFFICE OF RESEARCH AND
DEVELOPMENT. ENVIRONMENTAL PROTECTION TECHNOLOGY SERIES
Coden: EPTSBT Publ.Yr: May 198O
tllus. refs.
Abs. (Available from NTIS. Springfield. VA 22161)
Languages: ENGLISH
The RO system described functions by concentrating the
chemicals for return to the processing bath white purifying
the wastewater for reuse In the rinsing operation. The
effectiveness of the PA-3OO, PBIL, NS-IOO, NS-2OO, SPPO. B-9,
and CA membranes were evaluated In tests on rlnsewater with
extreme pH and oxldant levels. The PA-3OO membrane performed
well with copper cyanide, zinc cyanide, and chromic acid
rlnsewaters. while the NS-2OO and PBIL membranes performed
best with acid Cu rlnsewaters. After commercializing the
membranes, applications In various metal finishing,
non-ferrous metal, steel, and Inorganic Industries may be
found. (FP.AM)
Descriptors: Reverse osmosis; Membranes; Wastewater
treatment; Metal finishing Industry wastes; Waste treatment
Identifiers: electroplating rtnsewater
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DIALOG Mle41: Pollution Abstracts - 7O-B2/Apr (Copr Cambridge Scl Abs) (Item 11 of 61) User23913 23JunB2
U)
(O
Ul
8 I-OO4OO
Calorlmetrlc studies of b lodegradatIon processes In
biological uastewater treatment.
Fortler, d. -L.; Reboul. B.; Philip, P.; Slmard, M. -A.;
Picker, P.; Jollcoeur. C.
• Unlverslte de Sherbrooke, Centre d'ApplIcatIons en
CalorImetrie et Thermodynamlque. Sherbrooke, Quebec J1K 2R1,
Canada
WATER POLLUTION CONTROL FEDERATION. JOURNAL 52(1), 89-97,
Coden: JWPFA5 Publ.Yr: dan 198O
Ulus 25 refs.
1 Eng., Fr., Ger., Port., Span. abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The heat associated with blodegradatIon reactions In culture
suspensions was Investigated by using flow mlcrocalorImetry.
Bacterial cultures obtained In batch or continuous recycling
processes (activated sludge) were mixed with synthetic
biodegradable effluents, and the heat output was monitored as
a function of time. With batch cultures, experiments were
conducted at various growth stages and COD levels. The
response of both types of cultures to a sudden change In the
COD content of the effluent and to the addition of toxic
contaminants (e.g.. cyanide, Cd, Cr, Cu. and phenol) was also
studied. The heat flux measured Is In general accordance with
the data obtained by resplroraetrIc techniques. Moreover, the
fast response of the flow mlcrocalorImeter makes It possible
to follow the kinetic response of the system after composition
changes. The calorImetrIc method shows promise for
applications In the control of biological wastewater
treatment. (AM)
Descriptors: BlodegradatIon; Biological treatment;
Wastewater treatment; Activated sludge process; Bacteria;
Measuring methods; Monitoring methods; Engineering; Kinetics;
Oxygenatlon; COD; Effluents; Absorption spectroscopy
Identifiers: calorlmetry
BO-O7619
The Environmental Impact of refinery effluents (EIRE study):
CONCAWE's assessment.
Bolsvleux, P.; Bonnier, P. E ; Goethel, G. F.; Jenkins, R
H.; Lemlln. J. S.: Lev!. J. D.; Marmln. A.; Paululs. C. D. A.;
Rotter I, S-; Slbra, P.; Verschueren, K.
CONCAWE. Water Pollution Management Group, The Hague.
Nether Iands
STICHTING CONCAWE. REPORT Coden: CONRD3 Publ.Yr. Feb
198O
11lus. no refs.
Sum.
Languages: ENGLISH
Doc Type: REPORT
The environmental Impact of refinery liquid effluents Is
reviewed. Refinery effluents In general are not a major
source of pollution because of substantial achievements by the
oil refining Industry In reducing hydrocarbon discharges. The
existing parameters. as measured by current techniques.
provide an adequate assessment of refinery effluent quality.
Recent legislative proposals designed to control the
concentration of specific compounds would be difficult to
Implement for refinery discharges. Most hydrocarbons display
short life under normal environmental conditions. High
molecular weight compounds, e.g., polynuclear aromatlcs which
persist for some time, can be reduced to prevailing background
levels by modern effluent treatment techniques. Heavy metals
can also be reduced to background levels In water treatment
plants at refineries. Other pollutants found In refinery
effluents (phenols. NH3, sulfldes, and cyanides) are normally
reduced by preliminary treatment and can be further reduced to
very low levels by biological treatment. (FT.MS)
Descriptors: Environmental Impact; Refineries; Effluents:
Hydrocarbons; Petroleum Industry; Aromatic compounds; Heavy
8O-O7559
A process for simultaneous removal of cadmium and cyanide.
Poon, C. P. C.; Soscla, K. P.
Univ. of Rhode Island. Kingston. RI O2881
INDUSTRIAL WATER ENGINEERING 17(2). 28-3O, Coden:
IWEGAA Publ.Yr: Mar-Apr 198O
Illus. refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
A compact reactor was used In which seawater or sodium
chloride solution was electrolyzed below a column of metal
finishing waste containing both cyanide and Cd. The chemicals
generated from the seawater electrolysis rose In the reactor.
bringing about reactions that completed the treatment process.
A combination of lower power Input and a deeper wastewater
column Is more effective In treatment. Several series of
experiments were conducted. For experiments using lower Cd
concentrations, values were obtained <4.189 mg/kWh with the
lowest one at *2,OOO mg/kWh. The effect of Initial Cd
concentration Is Illustrated. Greater removal per unit power
consumption was achieved with greater rinse water depth. (FT)
Descriptors: Cyanides; Cadmium; Heavy metals; Contaminant
removal; Seawater; Laboratory methods; Electrochemistry: Metal
finishing Industry wastes; Wastewater treatment
Identifiers: electrolysis
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DIALOG Flle4l: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 14 of 61) User239t3 23junB2
3204
CO
N)
8O-O75O6
Cyanide problems In municipal wastewater treatment plants.
lord*-. D. T. ; Lue-HJng, C. ; WhHebloom, S, W. ; Kelada. H. ;
Dennlson, S.
Metropolitan Sanitary District of Greater Chicago, Research
and Development Dept,, IOO E. Erie St., Chicago, It 6OGII
51st annual conference of the Water Pol tut Ion Control
Federation Anaheim, California Oct 1-6, 1978
Water Pollution Control Federation
WATER POLLUTION CONTROL FEDERATION, JOURNAL 52(3).
597-6O9, Coden: JWPFA5 Publ.Yr: Mar 198O
11lus. refs.
E ng., F r.„ Ger., Por t., Span. abs.
Languages: ENGLISH
Ooc Type: JOURNAL PAPER CONFERENCE PAPER
Data from daily monitoring of wastewater effluents from the
treatment plants of the Metropolitan Sanitary District of
Greater Chicago Indicated that a 11 effluents occasionally
exceed the limit of 0-O25 mg cyanlde/L set by the Illinois
Pol Hit ion Control Board. Of the larger plants serving
industrialized areas, the Calumet plant, which receives wastes
from 5 major steel mills, averaged O.O95 mg/L. and plants
serving electroplating Industries had averages of O.O27-O.O7
mg/L. The major proportion of the cyanide Is in the complex
form. The plants serving Industrlal areas averaged
O.OSO-O.O96 kg cyanide removed per gnflHHter treated
wastewater. A revised standard for discharges to 1111nois
waters of O. ID mg/L was established as a total cyanide monthly
average and O.2O mg/L for arty 24-hr composite. (AM)
Descriptors: Cyanides; Wastewater treatment plants;
MtmtcIpal wastewaters; 111 toots; Industrial wastes; Toxic
mater ials
Ident Iflers: Chicago; MetropolI tan Sani tary District of
Greater Chicago
feasible, the proposed alternative approach centers on setting
limits on certain, more commonly regulated, parameters which
can be agreed upon and which will not result In great Iy
Increased compliance monitoring costs. Certain parameters
(TSS, BOO. cyanide, etc.) will be used as indicators of toxic
pollutants. While the verdict Is not yet delivered concerning
this approach. the trend seems to be toward permi t
consoltdat ton, or the * 'one stop'' permi t. Another Ini t iat *ve
aimed at '"forcing'' technology, and curbing violations may
well be the increased use of criminal statutes to enforce laws
and regulatIons. Under these guide IInes, most str tngent
action would be taken against violators when health and
environmental damage or risk are great (especially If the
discharge violations involve toxic or hazardous pollutants),
when data are withheld for falsified. or where there are
flagrant cases of wltIful or negligent misconduct. (FT)
DescrIptors: Wastewater treatment; Government regulat ions;
Leg!slat ion; Pollut ion control; Industrlal effluents;
Technology; EPA; Toxic materials
IdentIf iers: best avallable technology economically
ach1evabIe
8O-O7031
Does the permit system force technology?
Josephson, J.
E S & T, 1155 Sixteenth St NW, Washington, DC 2OO36
E S « T 13(8), 911-912. Coden: ESTHAG Publ.Vr: Aug
1979
no refs.
No abs.
Languages- ENGLISH
Doc Type: JOURNAL PAPER
''Forcing'' may be defined either as compelling the use of
known technology, which might not otherwise be used to meet
guidelines, or as pushing water pollution control technology
beyond Its present 1imtts. Cases in which the
state-of-the-art might have to be pushed occur where
regulations require that discharges may have to meet standards
of ''best avallable technology economically avallable'' by
1984-87. One example of absolute requirements for this
involves treatment requirements for any effluent contaIntng
toxic substances. To control toxics. EPA suggests the direct
1 irni tat Ion of spec* f Ic to* icants , where feas Ible. When not
-------
DIALOG F1le4l- Pollut(on'Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 16 of 61) User239t3 23jun82
8O-O6267
Kinetics of reaction of cyanide and reduced sulfur species
In aqueous solution.
Luthy. R. G.; Bruce. S. G.. Jr.
Carnegie-Mellon Univ., Dept. of Clvlt Eng. . Pittsburgh, PA
15213
E S '& T 13(12). 1481-1487. Coder): ESTHAG Publ.Yr:
Dec 1979
iI lus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Interactions of cyanide and reduced S species In aqueous
solution 'can produce thlocyanate. Kinetics of the reactions
of cyanide and polysulflde and cyanide and thlocyanate were
Investigated. The reaction of cyanide and polysulflde ts
mixed order and the order decreases from 1.9 to 1.3 as pH
Increases from 8.2 to 12; this Is largely accounted for by a
decrease In reaction order with respect to cyanide as pH
Increases above the pKa for hydrogen cyanide. Catalysis and
Inhibition studies showed that high concentrations of NH3 were
inhibitory and that coal char fines were catalytic. The rate
of reaction of cyanide and polysulftde Is °»> = 3 orders of
magnitude faster than reaction of cyanide and thtosutfate
depending on pH value. A neutral or slightly alkaline
solution containing the order >=1O-3 M total sulflde may form
polysulflde on exposure to O2 and In the presence of cyanide
there should be reaction to yield thlocyanate. (AM)
Descriptors: Kinetics; Cyanides; Sulfur compounds;
Wastewaters; Chemical reactions; Coal conversion; Oxidation;
CatalysIs
Identifiers: thlocyanate; coke effluents; sulflde
8O-O6231
A practical approach to uastewater treatment for the metal
finishing Industry.
Olthof. M.
Duncan, Lagnese and Assoc.. Inc., 3185 Babcock Blvd..
Pittsburgh. PA 15237
WATER POLLUTION CONTROL ASSOCIATION Of PENNSVLVANIA.
MAGAZINE 12(6). 18-27, Publ.Vr: Nov-Dec 1979
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type. JOURNAL PAPER
General guidelines for the development of a pollution
control program for a metal finishing plant are provided.
In-plant considerations for the design of a treatment system
Include water flow reduction, optimizing the dilution ratio,
counterflow rinsing, cascade rinsing, segregation, process
solutions, floor spillage, and dragout reduction. Practical
treatment methods Include hexavalent chromium treatment,
cyanide treatment, and general rinse water treatment
Reference Is made to promising new technologies and their
potential application. The chemistry outlined forms the basis
for tiie design of wastewater treatment facilities. A typical
flow schematic for & metal finishing plant Is presented.
Miscellaneous treatment approaches include Integrated system,
Ion exchange. and RO. The potential for recovery of one of
the plating solutions should be evaluated during the planning
stage for pollution control.fad I Ities; Ni, Cr, Cu. and Zn
plating baths are possibilities. (FT)
Descriptors: Metal Industry wastes; Wastewater treatment;
Pollution control; Engineering; Ion exchange: Reverse osmosis;
Chromium; Cyanides
Identifiers: metal finishing Industry; hexavalent Cr
treatment; cyanide treatment; general rinse water treatment
8O-O6I58
Removal of Inorganic pollutants from wastewater during
reclamation for potable reuse.
Smith, R.; Slebert, M. L.; Hattlngh. W. H. J.
CSIR. National Inst. for Water Research. P.O. Box 395.
Pretoria OOO1, South Africa
WATER S. A 6(2). 92-95, Coden: WASADV Publ.Vr: Apr
I98O
IIlus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The effectiveness of a pilot water reclamation plant for
removing certain toxic and aesthetically undesirable inorganic
chemical constituents from wastewater designed for potable
reuse Is described. Process stages Include high lime
treatment, primary clarification, ammonia stripping, secondary
clarification, sand filtration, chlorinatIon, and activated
carbon adsorption. The high lime and activated carbon
treatments were the most significant for the removal of Cd,
Cu, Pb, Hg, and Zn, while the chlorlnatlon stage was the most
effective for cyanide removal. High lime treatment alone was
sufficient for the complete removal of highly toxic Cd and Pb
Concentrations of all 6 substances Investigated were reduced
to below the detection limits of the analytical methods used.
(AM.FT)
Descriptors. Cyanides; Wastewater treatment; Pollutant
removal; Heavy metal£; Pilot plants; Toxic materials;
Inorganic compounds; Potable waters; ChlorInation; Mercury;
Activated carbon; Engineering; South Africa; Cadmium; Copper:
Lead; Zinc
Identifiers: Pretoria; Stander Water Reclamation Plant
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DIALOG Flle41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 19 of 61) User23913 23Jun82
LO
M
CD
8O-O6116
Bench-scale testing for residual waste treatment.
Vuceta, J. ; Anderson, J. R.; TeKlppe. R. J.; Catkins, R. J,;
Bishop, W. J.
James M. Montgomery Consulting Engineers, inc., 555 E.
Walnut St., Pasadena, CA 91101
BOth annual conference of the Water Pol tut Ion Control
FederatIon Philadelphia, Pennsylvania Oct 2-7, 1977
Water Pollution Control Federation
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5I(1O).
2366-2383, Coden: JWPFA5 Publ.Yr: Oct 1979
11lus. refs.
Eng.. Fr.. Ger., Port., Span. abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER CONFERENCE PAPER
The most ef feetIve technologies for central I zed treatment of
varlous Industrlal res Idual wastes generated in Ventura
County. California, were determined. Steps required for a
successful treatment of metallic wastes Include cyanide and
cyanate oxidation, Cr (VI) reduction, hydroxide and sulftde
precipitation, coagulation and flocculatIon, and filtration.
Ion exchange and carbon sorptlon are not usually required.
Coagulation and flocculatIon of nonmetallie toxic wastes,
followed by filtration and carbon sorptlon. Is more effective
In the removal of1 toxic nonmetal11c substances from
wastewaters than foam fract ionatIon coupled with carbon
sorptlon. A batch mode of operation Is superior to continuous
flow. (AM)
Descriptors: Waste treatment; Filtration; Heavy metals;
CoagulatIon; Flocculat ion; Industrial wastes; Wastewater
treatment; Cyanides; CalIfornla; Ox Ida11on; PrecIpI tat Ion;
Toxic materials
Ident if iers: bench-scale test Ing; Ventura County
8O-O5527
Industrial pretreatment.
Her Itage, J.
EPA Journal, 4OI M St. SW. Washington, DC 2O46O
U.S. ENVIRONMENTAL PROTECTION AGENCY. EPA JOURNAL 5(7),
17-18, Coden: EPAJOB Publ.Vr. Jul-Aug 1979
no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The cleanup program announced by the EPA will remove toxic
chemicals, e.g., cyanide, hexavalent Cr, Cd, and. Pb, from
Industrial wastes currently being discharged Into municipal
plants. The pretreatment standards wl11 affect =3O,OOO
Industrlal plants. cover 34 major Industrlat types, and
control discharges off 129 toxic Industrial pollutants. The
standards will set numerleal limits on the quant 11les of
spec If ic pot 1utants that can be discharged by a plant In an
Industry category To sfmplIfy the pretreatment Job. EPA Is
demonstrating new technology To back up the pretreatment
action. the Clean Water Act, Clean Air Act, RCRA. and TSCA
will be Implemented (FT)
DescrIptors: EPA; Federal regulatIons; ToxIc mater la Is;
Chemicals; Industrial wastes; Water pol1utants; Wastewater
treatment plants; Technology; Effluent standards
IdentIfIers: cleanup program; RCRA; TSCA
8O-O4756
Electrodfalysls of effluents from treatment of metallic
surfaces.
Kagaku Kojo. Feb 1979. Translated by Bureau of Reclamation.
Denver„ CO
Itol. S.
Asahl Glass Co., Specialty Chemicals and Plastics Marketing
DIv., 1-2-1 Marunouchl, Chiyoda-ku, Tokyo, 1OO Japan
DESALINATION 28(3), 193-2O5, Coden- DSLNAH Publ Yr:
Mar 1979
(1 lus. refs.
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Eleetrodlalysis Is applled for treatment of effluents front
washing after galvanization. and specifically from washing
after Ni gatvanizat ion. This method Is useful for recovery of
galvanlzatIon reagents used In varlous processes.
E1ec t rod1a Iys1s Is probab1y app1 Icab1e for t reatment o f
ef fluents from washIng af ter cyanIde ga1 van i za 11on or
galvanization with.other substances. To establish a closed
system for the effluents discharged durIng the treatment
processes for metal 1Ic surfaces, techniques for
Industrialization of electrodialysls were developed not only
for the recovery of usefuI components, but a 1 so for recyc1ed
use of water. IndustrialIzatIon of electrodialysls is
expected in the near future. To establish these techniques.
technIca1 deveIopment • 1s needed no t on t y In 1on-exchange
membranes and electrodlalyzers, but also in systemat tzed
processes, including all related techniques. eg,.
pretreatments. (MS)
Descriptors: Industrial effluents; Metal finishing industry
wastes; Water recyclIng; Dialysis; Materials recovery;
Etectrochemlstry; Wastewater treatment
Ident ifiers: electrodialysls; galvanization
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DIALOG Flte4l. Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 22 of 61) User239l3 23Jun82
BO-O4557
Cyanide and thlocyanate In coal gasification wastewaters.
Luthy, R. G ; Bruce, S. G. . Jr.; Walters. R. W.; MaMes, D.
U.
Carnegie-Mellon Univ , Dept of Civil Eng., Pittsburgh, PA
15213
WATER POLLUTION CONTROL FEDERATION. JOURNAL 51(9).
2267-2282. Coden. JWPFA5 Publ.Yr: Sep (979
I Ilus. refs.
Eng., Fr., Ger.. Port., Span. abs.
Languages• ENOLISH
Doc Type: JOURNAL PAPER
Procedures for preservation and Identification of cyantde
and thfocyanate In coal gasification wastewater, possible
pathways for aqueous-phase formation of thlocyanate, and
reaction of cyanide and polysulfIde-S to produce thlocyanate
were Investigated. Cyanide preservation procedures require
removal of sulfide and high levels of carbonate. An
analytical procedure for thlocyanate determination based on a
Cu-pyrldtne coloMroetrtc method with preextractIon was tested
successfully on most samples. The reaction of cyanide with
polysulfIde-S was =1.54t/-o.2S with a rate constant of =O.24
(M/L)-O.54/mln. Control of cyanide polysul f Ide reaction
requires selective control of sulfide oxidation kinetics. (AM
)
Descriptors: Wastewaters: Cyanides; Energy sources; Coal
gasification; Chemical reactions; Absorption spectroscopy;
Organosulfur compounds; Oxidation; Contaminant removal
Identifiers: thlocyanate; polysulflde; preservation
BO-OI965
Hydrogen peroxide In sewage treatment.
Sims. A. f. E.
Interox Chemicals, Ltd., Moor-field Rd. . W! dries, Cheshire WAS
OUU, England
ENVIRONMENTAL POLLUTION MANAGEMENT 9(4), IO7-I1O.
Coden. EVPMBX Publ.Vr. Ju'l-Aug 1979
11lus. no refs.
ISSN: O367-I5OX
No abs.
Languages: ENGLISH
Doc Type JOURNAL PAPER
TREATMENT COOES: O .(DESCRIPTIVE) ; M .(METHODOLOGICAL) ; A
.(APPLICATIONS.)
The most notable advantage of using hydrogen peroxide (H2O2)
In wastewater treatment Is Its ability to control the odor and
corrosion problems caused by H2S. Hydrogen peroxide converts
available sulfide to Inert S and provides a preferential
source of consumable O2 to prevent further sulfide formation.
The preferred method of administration Is by injecting the
11202 directly Into the main using a positive-action metering
pump operating In conjunction with the sewage flow. It can
also be used to control sulfide In sludge as welt as upgrade
biological oxidation systems. In treating Industrial
effluents, H2O2 oxidizes cyanide to relatively nontoxlc
cyanate and btodegrades phenols. (FT)
Descriptors: 'Oxldants; Wastewater treatment; Chemical
oxidation; Odors; Corrosion; Hydrogen compounds; Contaminant
removal
Identifiers: hydrogen peroxide
toxic electroplating
8O-OI928
Methods for neutralizing
rlnsewater-part 3.
Marin, S.; Trattner, R. B.; CheremlsInoff, P. N.
New Jersey Inst. of Technology, Newark, NJ O7 |O2
INDUSTRIAL WASTES 35(5). 22-23. Coden: INWABK
Publ.Yr: Sep-Oct »979
refs.
ISSN: O537-5525
No abs.
Languages: ENGLISH
Ooc Type: JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; D .(DESCRIPTIVE)
In ' the removal of Cr from electroplating rlnsewater, the
treatment Is Intended to convert Cr+6 to Cr + 3, and then to
precipitate It as the Insoluble hydroxide. The reduction is
performed with sodium bisulfite (NaHSO3) at a pH of 2.O, with
the precipitation occurring at pH 8.5. using caustic for the
pH adjustment. A pH recorder-controller Is used to measure
the pH and add the NaHSO3 under automatic oxidation-reduction
potential (ORP) control. When the ORP Indicates a value of
3OO mV, the chromates are reduced. and the addition Is
stopped. After 15 mln of mixing, the pH Is adjusted to 8.5.
and after = 15 mln of additional stirring. the precipitated
hydroxides are allowed to settle. In the removal of cyanide
and alkali wastes, the cyanides are 1st converted to cyanates
with a 15% solution of sodium hypochlorite (NaOCl) at a pH
>1O. and are then oxidized to N and CO2 with the NaOCl
solution at pH 8.5. When the ORP reaches a range of 35O-4OO
mV (indicating that all cyanides have been oxidized) the
wastewater changes from a clear, transparent green to sky
blue. Complete oxidation takes =1O mln. The treated water Is
allowed to settle for = 2 hr, during which time small amounts
of metals, e.g., Cu and Ag. will be precipitated as Insoluble
hydroxides. (FT)
Descriptors: Industrial wastes; Wastewater treatment;
Chromium; Cyanides; precipitation; Chemical oxidation;
Reduction; pH; Metals; Toxic materials
Identifiers: electroplating rinsewaters; automated control;
sodium bisulfite; sodium hypochlorite; hydroxides
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DIALOG F1le4(- Pollution Abstracts - 7O~82/Apr (Copr. Cambridge Sc I Abs) (Item 25 of 61) User23913 23junB2
CO
U>
O
ao-ot866
Methods for neutralizlng
r i nsewater-part 1.
Mar In, S.; Trat tner, R. B,; Chereraislnoff. P. N.; Perna. A.
toxic electroplating
New Jersey Inst. of Technology, Newark, NU O71O2
INDUSTR1AL WASTES 25(3), 5O-52. . Coden: INWABK
Publ.Yr; May-Jun 1979
11lus. no ref s.
ISSN- O537-5525
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: M .(METHODOLOGICAL) ; A .(APPLICATIONS) ; D
.(DESCRIPTIVE)
R1nsewat er s f rom the e1ec t rop1 a 11 ng process conta In high
concentrations of cyanides and chromates. To comply with US
EPA d1scharge standards severa1 chem1ca1 processes have been
developed to destroy the cyanides and chromates. For cyanide
the most common form of treatment Is alkaline chlortnatlon
oxidation by sodium hypochlorite or CI2 plus sodium hydroxide
add It Ion to the waste. Electrolytic decomposition and
ozonation are also effective treatments for cyanide wastes.
Chromium waste treatment Involves reduction and precipitation
processes. Reducing agents Include ferrous sut fate, sod Iurn
blsutfate. and sulfur dioxide; neutralizing compounds Include
lime slurry or caustic. Batch treatment Is necessary in shops
having a total dally flow <30,000 gpd, whereas continuous
treatment Is recommended for volumes >3O,OOO gpd. (FT)
DescrIptors: Metal finishing Industry wastes; Cyanides;
Chromium compounds; Wastewater treatment; Contaminant removal;
Chemlea I ox IdatIon; NeutralIzatIon; ReductIon f
IdentIf iers: electroplatIng
which gave a complete kill In =3O sec, while 5.O mg/L of Cl
failed to give & complete kill after 5 mln of contact time.
As an oxldant, CIO2 Is selective to some compounds considered
wastewater potlutants. SulfIde-containlng gases and waste
produc t s 'of petro1eum refIn ing, coa\ cok1ng, b1ack I1 quor
evaporations, viscose rayon manufacturing, and natural gas
purification are frequently scrubbed with alkaline solutions
and require treatment before discharge. Between pH 5.O and
9.O an average of 5.2 parts by weight of CIQ2 oxidizes t part
by weight of H2S, expressed as sulflde ion. Instantaneously to
the sulfate ton. C1O2 oxidizes simple cyanide to cyanate
and/or CO2 and N. It can also be used over a wide pH range and
In organic contaminated systems for btocontrol and for the
control of industrial odors. These capabt11tles, combined
wi th an on-si te technology that adapts eastly to ex 1st Ing
process facilities, make it a logical choice when considering
wastewater treatment alternatives. (FT)
Descriptors: Chlorine compounds; Wastewater treatment;
DIsInfectants; Ox IdatIon; Water treatment; Odors; Pollutant
removal
Identifiers: chlorine dioxide
8O-O1856
Disinfection and oxidation of wastes by chlorine dioxide.
Rauh. J. S.
OHn Corp., Olin Water Services. 3155 Flberglas Rd. . Kansas
City. KS 66t15
JOURNAL OF ENVIRONMENTAL SCIENCES 22(2), 42-45, Coden:
JEVSAG Publ.Vr: Mar-Apr 1979
11lus. refs.
ISSN: OO22-O9O6
No abs.
Languages ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL)
Although in acidfc, organic-free environments. Cl shows a
slight advantage over chlorine dioxide (C1O2) (n dosages
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DIALOG Ftle4l: Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge Sc I Abs) (Item 27 of 6O User23913 23JunB2
CO
CO
525B9-B2629.
Coden FEREAC
G .(GENERAL OR REVIEW)
regulation
8O-O1339
Effluent guidelines and standards; electroplating point
source category; pretreatment standards for existing sources.
c/o E. P. HaU. Effluent Guidelines Olv. (WH-652), 4OI M St.
SW. Washington, DC 2O46O
FEDERAL REGISTER 44(175).
Pub! .Yr: Sep 7, 1979
H lus. no ref s .
Sum .
Languages: ENGLISH
Ooc Type: JOURNAL PAPER
TREATMENT CODES: D .(DESCRIPTIVE)
W .(NEWS)
Effective Oct. 9. 1979. this regulation limits the
concentrations or mass and requires pretreatment of certain
pollutants that may be Introduced Into publicly owned
treatment works by operations In the electroplating point
source category. For plants with a flow of >=38,OOO L/d, the
promulgated standards specifically limit Indirect discharges
of cyanide, Pb. Cd. Cu, Nl. Cr, Zn, and Ag, and total metal
discharge, the sum of the Individual concentrations of Cu, Nl,
Cr, and Zn. For plants with a process wastewater flow of
<38.OOO L/d. these standards 1 Iml-t only Pb, Cd. and cyanide.
The specific numerical limitations are given. (FT)
Descriptors: EPA: Federal agencies; Federal regulations;
Wastewater discharges; Metal finishing Industry wastes;
Cyanides; Heavy metals: Water pollutants; Industrial effluents
; Effluent standards
Identifiers: final rule; electroplating point source
category
control parameters In the treatment of water and wastewater
are flow rate, level, pH, oxidation-reduction potential. and
residual Cl. Additional parameters commonly used to evaluate
the degree -of treatment Include conductivity, temperature,
turbidity, and DO. Several other parameters are measured
using more sophisticated methods, e.g.. Ion selective
electrodes and cyanide and TOC analyzers. These methods are
relatively new and generally require pretreatment of the
sample to remove Interfering agents In free or combined form
or to change the parameter to a more desirable one. All the
systems described share the common goals of releasing the
operator from manually making adjustments and providing for
more efficient use of chemicals and energy. (FT)
Descriptors: Wastewater If-eatment plants; Water treatment
plants; Monitoring Instruments; Engineering; Data systems;
Technology
Identifiers: automated control
8O-OO487
Plant demands require reliable Instrumentation.
McClaln. T. L.; Goswaml. S. R.
R. E. Warner S Assoc.. 2130 W. Park Dr.. Loraln. OH 44OS3
WATER AND WASTES ENGINEERING 16(2), 26-31. 66-67,
Coden: WWAEA2 Publ Yr: Feb 1979
11lus. refs.
ISSN: OO43-115X
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; A .(APPLICATIONS)
Available control parameters for wastewater treatment plants
are listed, and their applications are discussed. The
closed-loop system, the pacing system, and the radio
controlled system are schematically diagrammed. The
closed-loop system Is comprised of a process; a measuring
subsystem; and a controlling subsystem consisting of the
controller, the final control element, and the control agent.
The pacing system Involves the controlled feeding of a
''slave'' material In proportion to the ''master'' material.
This system can be modified to a true automatic loop by
developing a radio control system In which both flows are
measured and brought to a radio controller system where their
quotient Is compared to the desired ratio. Major process
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DIALOG File-It: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sci Abs) (Item 29 of 61) User239l3 23junB2
32 IO
OJ
W
•to
79-O6686
Photo processing sludge; New Cornstock lode?
Frank. A.
Sludge Magazine, P.O. Box IO67. Silver Spring. MD 2O9IO
SLUDGE MAGAZINE 2(1). 22-26. Publ.Yr: Jan.-Feb. 1979
illus no refs
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The combination of new technologies, favorable economics,
and stringent pollution controls is leading to In-plant
recovery. especially wfthln the photoprocessIng Industry.
There Is no typical photographic processing effluent,
according to the Industry's trade association, but faced with
the possibility of Industry-wide regulation under the Federal
Water Pollution Control Act, the trade association sponsored
the ANSI development of a standard to Identify those
substances which might be present and establish acceptable
analytical techniques. The standard identifies 30 elements
and characteristics that may be found In photo processing
effluent. Only Ag and total cyanides have received regulatory
cognizance to date. Effluent standards designed to restrict
direct discharges of Ag and cyanides were established by the
EPA In July 1976. New standards are expected from the EPA by
Feb. 1, 198O. which could be so stringent as to preclude
large concentrations of Ag and cyanides from accumulating In
municipal treatment plant sludge. Many photo processors are
not waiting for EPA's new regulations for reasons of
economics. Silver. at $1.25-$5/oz. is reason enough to
pretreat wastewaters. Eastman Kodak Company markets a simple.
Inexpensive Ag recovery system suitable for smaller
processors. Pilot tests using a 2-stage disposal cartridge
filtration system had a Ag recovery of 99.99%. Filter press
and sludge evaporation techniques are examined. To assess the
leaching potential of Ag and ferrocyanlde column tests were
performed under conditions simulating landfill; Ag and
ferrocyanide were released from sludges in particulate form
only and were rapidly filtered and bound within the soil. (FT
)
Descriptors: Economics; Technology; EPA; Silver; Cyanides;
Materials recovery: Photography; Leaching; Feasibility studies
; Federal regulations; Industrial effluents
Identifiers: Eastman Kodak Co.; Federal Water Pollution
Control Act
Doc Type: JOURNAL PAPER
The efficiency of the 2nd stage activated sludge treatment
of coke plant effluents depends substantially on an effective
quality equalization of the wastewater and consistent ammonia
(NH3) stripping pretreatment. In a pilot plant study, warm
weather conditions favored the necessary NH3 oxidation. The
studied system showed J9O% NH3 oxidation and was characterized
with very fast recoveries from shock NH3 loadings. The mixed
liquor temperature was an Important factor affecting the
performance of the nitrification unit. An effective
nitrification can be achieved under winter conditions with the
application of a heating system In the aeration tank. (FT)
Descriptors: Activated sludge process: Coke; Industrial
effluents; Biological treatment; Cyanides; Ammonia;
Nitrification; Pilot plants; Laboratory methods: Wastewater
treatment
Identifiers: coke plant effluents
79-O6677
Second-stage activated sludge treatment of coke-plant
effluents.
Gariczarczyk, J. J.
Univ. of Toronto, Dept
Ontario MSS 1A4. Canada
WATER RESEARCH 13(4).
Publ.Yr: 1979
Illus. refs.
Abs.
Languages ENGLISH
of Civil Engineering, Toronto.
337-342. Coden: WATRAG
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DIALOG FHe41: Pollution Abstracts - ?O-82/Apr (Copr. Cambridge ScI AbsI (Item 31 of 61) User23913 23jun82
CO
lx)
OJ
79-O4997
The Impact of toxic pollutants on disposal from wastewater
systems.
Schwartz. H. G.. Jr.; Buzzelt. J. C.. Jr.
Sverdrup Corp., 8OO N. Twelfth Blvd., St. Louts, MO 631O1
INDUSTRIAL WATER ENGINEERING 15(6). I4-2O, Coden:
IWEGAA Publ.Yr: Oct.-Nov. 1978
Itlus. refs.
Sum.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
A broad overvlew Is provided o.f the current state of
knowledge regarding the effect's of tox Ic pol lutants of
publicly owned treatment works (POTWs) on the water, land, and
air environments to which they may ultimately be released.
The 65 classes of pollutants referenced In the Clean Water Act
contaIn 129 spec!fIc elements or compounds Ident1fled as
prlor Ity pollutants. These Include 13 metals and 114
organlcs. plus cyanides and asbestos. The need for
control 1 ing their discharge Is apparent. Many of them can
Interfere with the efficient operation of POTWs, or pass (
through them to affect the environment adversely Metals can ^
Inhibit biological processes or accumulate In waste sludges,
preventing them from being used for agricultural purposes. *
Incineration of contaminated sludges may release the metals to
the atmosphere, and leaching from landfills may return them to
the aqueous environment. Organlcs can have similar Impacts.
Some of them can be strIpped from the waste stream and
discharged to the atmosphere during waste treatment.'
EstablIshment of equltable pretreatment standards will be
difficult, especially In the area of organic compounds. There
Is little information available regarding sources, quantities.
treatabiltty. variability, health effects. and environmental
Impact of these pollutants at the low concentratIons
encountered, but EPA has embarked on an extensive program to
deveIop an adequate da ta base upon whIch to formulate
standards. (FT)
Descr fptors: Wastewater treatment plants; ToxIc materlals;
Organic compounds; Metals; Environmental Impact; Federal
regutatIons; Water qua!Ity standards; EPA
Identifiers: Clean Watdr Act
79-O3874
Pre-treatment of coke-plant effluents.
Ganczarczyk, J. J.
Unlv. of Toronto, Dept. of Civil Engineering, Toronto 181,
Ont. M5S 1A1. Can.
TORONTO. UNIVERSITY. DEPT. OF CIVIL ENGINEERING PUBLICATION
Coden: PUTED9 17 pp Publ.Yr: June 1978
Ulus. refs.
Abs.
Languages. ENGLISH
In the majority of North American coke-plants, the effluents
are composed of excess flushing 1iquor and condensates from
pr imary and f inal coolers and the benzol plant. At some
plants wastewaters from ammonium sulfate crystalIzatIon, tar
still, gas desulfurIzers and cyanide strippers contribute to
these effluents. The effluents contain biodegradable (BOD)
and non-biodegradable organlcs, spec IfIc organlcs (e.g.,
phenols), cyanide, thlocyanate, other minera 1 sulfur compounds
and ammonia. Their flow may vary widely depending on coal
moisture content and the specific design and operation of the
plant. The methods and strategies of pretreatment for
coke-plant effluents practIced In some typical plants are
discussed. A statistical analysIs of an ammonia stripping
tower performance Is also presented. Pretreatment of
coke-plant effluents seriously effects the performance of the
subsequent wastewater biological treatment (carbonaceous
oxidation and nitrification). An example Illustrates the
effectiveness of blohydrolysls of thlocyanate measured in a
fulI-scale treatment process and In ptlot-scale nitrification
exper Intents. (AM)
DescrIptors: Industrlal effluents; Wastewater treatment;
AmmonIa; BOD; Organ1c compounds; Cyan Ides; Coke; Sulfur
compounds; Nttrlftcatlon; Chemleal ox 1 da 11on
^9-03136
Waste water treatment at Climax.
Gott. R. D.
Climax Molybdenun Co., Climax Mine. Climax, CO 8O429
1977 Amerlean Mining Congress mining convent Ion. San
Francisco, Calif. Sept. 11-14. 1977
American Mining Congress: 1977 mining convention: Session
papers. Set No. 5. Environmental Controls I ft II 3O pp
Publ Yr: (n.d.)
Publ: Washington. D.C. American Mining Congress
11lus. no refs.
No abs.
Languages: ENGL 15(1
Doc Type: CONFERENCE PAPER
Process defInltIon for wastewater treatment at C1imax
Incorporates countercurrent Ion exchange for Mo removal,
followed by Swift electrocoagulatlon-electrof totat Ion for
heavy metals removal with a polIshlng f11ter for f inal
effluent clarification. Sodium hypochlor1te Is added prior to
the electrof totat Ion basIn as an oxldant for cyanide
destruction. Pilot scale operations Indicate essentially all
the Fe and Mn and K 9O% of the Zn, Cu, Mo, and cyanide are
removed. The Mo removed by the Ion exchange unit Is processed
by solvent extraction-crystallization producing a marketable
sodium molybdate. Skim electroflotatIon products will be chem
fixed and returned to the tailing area for Impoundment. The
inclusion and adaptation of the Swift Lectro Clear process to
treatment of process water at Climax is considered a first for
the mineral Industry. (MS)
DescrIptors: Molybdenum; Wastewater treatment; M ineral
recovery; Mining wastes; Ion exchange
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79-O3O61
Industrial applications of ozone.
Stopka, K.
U.S. Ozonalr Corp.
INDUSTRIAL WASTES 24(3). 23-24. Coden: INWABK
Publ.Yr: May-June 1978
1Ilus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
European and Japanese f tsherles use ozone (O3) for
stertlIzatIon purposes. Improved treatment of Industr tally
contaminated wastewater Is obtained by enriching the air used
for oxygenation with 5% 03. Sulfuric acid Is added to pH 2-4,
along with .OS-I g of ferric or aluminum chloride, followed by
alkaltzation to pH 6.5-7.5 with line. This precipitates most
organlcs. sol ve'nts. oils, res Ins, fatty esters, and toxic
metals. At a retention time of 6-1O mln, 2O mg/L of O3
usually will produce an effluent acceptable to most
environmental requirements„ Cyanide decompos11 ion can be
speeded up by as much as 1OO times through Cu catalysis. With
appropriate pretreatment, ozonatlon of composite wastewater
from a res in manufacturer reduced phenol from 272 to O.
formaldehyde from 376 to O. and total SS from 2.47O to 16O
mg/L. The COD In acidic wastewater from an edible oil
processing plant was reduced from 1O.5OO to 32O mg/L, a 96%
reduction. For industries requiring ultrapUre water, the
treatment system consists of an electrolytic coagulator tank,
a 2O1 filter, an Ion exchange bed. an O3 system with 2% O3
concentration from predrled air and efficient contactors able
to dissolve Instantly 1 mg/L 03 Into the 1iqutd. and an
act ivated carbon fIIter and O.2I filter on discharge.
IncorporatIon of an ozonatIon unlt before a RO unlt can
prevent membrane clogging. (FT)
Descriptors: Ozonatlon; Wastewater treatment; Engineering
of metal hydroxides, followed by land fill dlsposItIon. A
schemat1c diagram of such an effluent treatment plant Is
presented. Applled research for the Polish metal f inlshlng
Industry Is conducted by the Institute of Precision Mechanics,
In Warsaw, which has developed several new effluent treatments
and material recovery techniques. The most promising Include
evaporative recovery of plating bath constituents from rinse
waters, RO systems for some plat Ing soJut Ions, 'improved Ion
exchange systems for single metal recovery from separated
rinse streams, secondary polishing systems for final effluent
purlfIcat Ion. rinse 'water purification steps prior to
evaporative recovery of RO, foreign metal recovery and other
impur tty removal from metal fInlshlng solutIons,
ultraf11tratIon metHods for water reclamation. and
sol id If leatIon of metal fIntshfng sludges containing mlxed
metal 11c hydroxides. Other promising techniques Include
possible utilization of sulflde precipitation of heavy metals,
solvent rIns Ing, Ion flotat ion, C adsorptIon, and recovery of
metals from hydroxide sludges by solvent extraction. (FT)
DescrIptors: Metal fInlshlng Industry; Pollut ion control;
Materials recovery; Reverse osmosis; Ion exchange; Engineering
; Cleaning process; Heavy metals; Poland
Ident If1ers: plat ing Industry; Polish Inst1tute of Precis ion
Mechanics
79-O2832
A clean water project In Poland.
Kteszkowskf, M.; Jackson, G. S.
Inst of Precision Mechanics. Plating Effluent Treatment
Dept.. OO-967 Warsaw. Pol.
ENVIRONMENTAL SCIENCE & TECHNOLOGY 12(8), 896-899.
Coden- ESTHAG Publ.Yr: Aug. 1978
11lus. refs.
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Wastewaters produced In metal finishing operations contain
such pollutants as cyanides, chromates, .heavy metals, mineral
acIds, aIkalis, oils, greases, detergents, and organic
solvents. The most common effluent treatment consists of
well-known, conventional chemical procedures which can be done
e i ther contInuously or batch-wise. They involve several
operat ions, such as alkaline chlor inat ion of segregated
cyanide solutions, reduction of segregated chromate solutions.
and final neutralization of mixed effluents and precipitation
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79-OO693
Eva1ua t1on of EPA recommended treatment and controI
technology for blast furnace wastewater.
Wong-Chong, G. M.; Caruso, S. C.
Carnegie-Mel Ion Inst. of Research, 5OOO Forbes Ave.,
Pittsburgh. PA 15213
AMERICAN SOCIETY OF CIVIL ENGINEERS. ENVIRONMENTAL
ENGINEERING DIVISION. JOURNAL 1O4(EE2), 3O2-32I, Coden:
JEEGAV Publ.Vr: Apr. 1978
11lus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
An evaluation of the EPA-recommended technology for treating
blast furnace wastewater, esstenlaity SS removal and
rec trculatIon of water, Found the technology Inadequate to
produce effluent qual1ty In compllance with the 1977
guIdelInes that Include ammonia (NH3). cyanide (CN), and
phenol. The evaluatIon examined an extensive data base
consisting of reponses to a questionnaire, long-term plant
operation data, a field survey, and a literature review, while
the EPA effluent limitation guidelines were developed from a
very limited data base. Alkaline chlorination and gas liquid
mass transfer were examined for controlling NH3, CN, and
phenol. Suspended solids removal from the blast furnace
scrubber and cooler wastewater can be achieved by gravity
settling Effluent SS levels of about SO mg/1 can be reliably
achieved In clarlflers with the aid of a flocculant. The
water usage for scrubbing and cooling blast furnace can be
sIgnlfleantly reduced by conduct Ing materlal and energy
balances around the scrubber cooler system. The control of
the scrubber and cooler water pH may offer a feasible and
probably least costly alternative to controlling the NH3 or CN
and phenol content of the blowdown to comply with effluent
limitations at some blast furnace plants. The EPA-proposed
use of alkaline chlorlnatlon Is effective for the removal of
free CNs. but uses costly chemicals. This process will not
destroy the complex Iron cyanides and can create a problem by
releas Ing chloroorganlcs to the receiving .waters. In almost
all cases, once-through systems were within the 1977 limits
for all parameters except SS. (FT & SS)
DescrIptors; Technology; Wastewater treatment; Water
pollution control; Effluent standards; EPA; Furnaces; Cooling
waters; AmmonIa; Cyan1des; Organic compounds; Water reuse;
Chlorlnatlon; Suspended sol Ids; Scrubbers; pH
IdentIflers: phenol
proceedings. In PROGRESS IN WATER TECHNOLOGY 1O(1-2).
419-430, Coden: PGWTA2 Publ.Vr: 1978
Illus. refs. (Some In Ger.)
Sum.
languages: ENGLISH
Doc Type: CONFERENCE PAPER
The Ruhrverband ensures that the wastes ,of metal finishing
establIshments in the Ruhr catchment are recycled to the
chemical Industry; the sale of the wastes covers only
transportatIon costs, but there are sav tngs compared to
chemical precipitation and sludge disposal. Wastewater Is
treated In 118 mostly smalI plants. Cyanide and
chromate-contalnlng wastewaters must be collected separately
and pretreated. The central decontamtnatIon plant at
Iserlohn, and the central treatment plant at Helllgenhaus are
described. To supplement the system of wastewater treatment
plants 4 Impoundments were constructed In the Ruhr valley.
Inf luen
river a
7O:3O
water wo
artlf 1c
heavy me ta 1 s . Dur 1 ng 1 ow f 1 ow In the 1 ower Ruhr
ratio between clean water and treated wastewater of
s maintained on the average. From this mixture
ks abstract their water and prepare drinking water by
al groundwater recharge. (FT)
DescrIptors: Federal Republ1c of Germany; Metal fIntshing
Industry wastes; Effluent treatment; Wastewater treatment
plants; Industrial effluents; Municipal water supplies; Waste
reuse
IdentIflers: Ruhr valley
79-OO626
Wastewater from plating works-required pretreatment and,
disposal of concentrates.
Imhoff. K R
Ruhrverband und Ruhrtalsperrenvereln, KronprInzenstrasse 37,
43OO Essen 1, FRG
International conference on advanced treatment of wastewater
Johannesburg, S. Afrlea June 13- 17, 1977
Advanced treatment and reclamatIon of wastewater: Conference
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79-O0591
The Sulfex heavy metal waste treatment process.
Felgenbaum. H. N.
Permutlt Company. Inc.. E. 49th St. and Midland Ave..
Paramus. NJ O7652
Fifth annual industrial pollution conference Atlanta, Ga.
Apr. 19-21. 1977
Fifth annual Industrial pollution conference: Proceedings.
Edited by L. Delplno and A. Krlgman pp 629-642 Publ.Yr:
1977
Publ: McLean. Va. Water and Wastewater Equipment
Manufacturers Association
Illus. no refs.
Abs.
Languages . ENGLI SI I
Doc Type: CONFERENCE PAPER
The Sulfex process removes heavy metals from solution In the
form of s- precipitates. The Iron sulflde (FeS) used as the
source of S- Is added to the system as a slurry prepared by
combining ferrous sulfate, a soluble sulflde, and lime. The
insoluble FeS forms a sludge blanket In a properly operated
precipltator which serves as a source of excess unreacted S-.
The metal residuals in the effluent are normally lower than
can be obtained by the hydroxide process. The Sulfex process
overcomes complexing and chelatlng agents. Hexavalent Cr can
be reduced and removed In one step along with other metals and
does not have to be segregated for pretreatment. Cost savings
may be realized by not having to use alkalis to raise pH above
B-9 as is necessary for hydroxide precipitation along with
additional acid to readjust the pH to acceptable discharge
range. Dual media pressure filters are provided for polishing
removal of SS carried over from the reactor. Cyanide bearing
wastes must be pretreated. (FT)
Descriptors: Heavy metals; precipitation; Effluent treatment
; Metal finishing Industry wastes; Wastewater treatment;
Industrial effluents; Sulfur compounds; Cyanides
Identifiers. Sulfex
DO. temperature, conductivity, redox potential, and turbidity
have been In use for many years In wastewater treatment
plants. Water equality monitoring systems composed of these
sensing systems with their associated amplifiers, recorders,
alarm circuits, and central data processors are in operation
In many countries. Many units are used at the outfall from
wastewater and sewage treatment plants for supervision of the
neutralization control loop. the effectiveness of the O2
control system of an activated sludge process, or the
efficiency of a final clarification stage. Some of the
available Ion-selective and gas-permeable membrane sensors
have immediate application to wastewater and sewage plant
control. The nitrate analyzer should be used for
determination of nitrate levels before and after
denitrIfIcatIon stages. It Is preferable to use 1 analyzer
with automatic switching of the 2 samples On Industrial
wastewaters, the F- and cyanide monitors have been used with
success. COO measurement has been automated. Because the
O.S-2 hr analysis time Is thought too slow for real time
control. or because correlation with BOD Is considered
Inadequate, other analyzers are being developed for TOC and
total C. (FT)
Descriptors: Monitoring Instruments; Wastewater treatment
plants; Sewage treatment plants; Water quality: Pollutant
analys is
Identifiers: automated control
79-OO496
The use of automatic analysers on waste water treatment
plant.
Meredith. W. D.
Kent-Belgium S.A., Place du Nouveau Marche aux Grains 1O.
1OOO Brussels. Bel.
International workshop on Instrumentation and control for
water and wastewater treatment and transport systems London
and Stockholm May 1977
Instrumentation and control for water and wastewater
treatment and transport systems: International workshop .
proceedings. In PROGRESS IN WATER TECHNOLOGY 9(5-6). 71-74.
Coden: PGWTA2 Publ Yr: 1978
11lus refs
No abs
Languages ENGLISH
Doc Type CONFERENCE PAPER
Continuous measurement and control of such variables as pH.
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DlAtOG File41. Pollution Abstracts - 7O82/Apr (Copr. Cambridge Set Abs) (Item 4O of 61) User23913 23jun82
78-O3385
Electrolysis.
Vlahakls. J. ; Ouellette, ft
E lecti-o techno logy: Vol . I: Wastewater treatment and
separation methods. Edited by R. P. Ouellette, J. A King and
P N Cheremlstnoff 193-237, Publ.Yr: 1978
Pub! Ann Arbor, Mich. Ann Arbor Science Publishers
1 Ilus. refs.
No abs.
Languages- ENGLISH
Doc Type: BOOK CHAPTER
The most important Industrlal applicatIons of electrolysis,
a chemical process by which chemical reactions are produced
electrically In solutions or molten salts, are metal recovery
and electroextract(on, electrochemical organic synthesis, and
electroconcentratIon of solids. Among many specific potential
applIcat ions are the manufacture of propylene oxide from
propylene and water, the treatment of acid mine drainage to
recover Fe. reducing the COD of cheese whey waste, the
recovery of fatty minerals from edible fats, the regeneration
of chromated Al deoxldlzers, the treatment of domestic wastes.
cyanide and organic waste treatment t and electroflotatIon.
E)ectroIyt fc processes produce less polJut ton than many
conventional techniques. and also compare favorably. on an
economic 'basis, with them. Electrolysis Is energy competitive
w1th other chemical routes for manufacturing chemical
compounds and, as environmental standards become more strict,
shoud become more popular in metal recovery and waste
treatment applIcatIons. (FT)
Descriptors: Electrochemistry; Reduction; Oxidation; Metals;
Wastewater treatment; Water purification; Organic wastes; Mine
dratnage; Matertals recovery; Chemical wastes; Waste treatment
; Technology
Ident1f iers: electrolys ts
78-O3333
Decontamination of water containing chemical warfare agents.
Ltndsten. D. C.
US Army Mobility Equipment Research and Development Command,
Petroleum/Environmental Technology Olv., Ft. Belvolr, VA 22O6O
AMERICAN WATER WORKS ASSOCIATION. JOURNAL 7O(2), 9O-92,
Coden: JAWWA5 Publ.Yr: Feb 1978
I Ilus. no refs.
Sum.
Languages. ENGLISH
Doc Type. JOURNAL PAPER
The maximum permissible concentrations (MFC) of chemical
agents In water serve as thresholds to determine contamination
and measure the success of decontamination. The presence of
chemical warfare agents In water can be determined by
detection kits, by dead fish or other aquatic life, unusual
odors from the water. an unusually high C1 demand, or
intelligence reports. There (3 presently no field method for
quantitative analysis of agents In water or for detection at
any level below the MPC F'or some agents, detection at the
MPC level is not available The standard army ERDLator water
purification unit ts ineffective when used directly against
most chemical warfare (CW) agents. A pretreatment procedure.
consisting of superchlor1natIon with 7O% calcium hypochlorlte
to fOO ppns available Cl, followed by a dechlorInatIon with 6OO
ppm of activated carbon, was developed, and proved effective
at removing CW agents to the MPC levels. Safe levels were
also achieved by distillation of water contaminated with HN-3
and HD (blister agents), but not with OA, GB. VX (nerve
agents), and AC (cyanide). RO was successful for removing
only sodium hydrogen arsenate. Waste slurries developed as a
result of using army field equipment should be disposed of
properly by burial, exposure to weathering processes, or
destruction by decontaminating chemicals. (FT)
Descriptors: Contaminant removal; Contaminants; Pollutant
detect ion; Chemtea 1 pollutants; Chior 1nat ton; Reverse osmos1s;
Distillation; Wastewater disposal
Identifiers: chemical warfare agents
78-O3214
Analysis of cyanides In coke plant Wastewater effluents.
Barton, P. J.; Hammer, C. A.; Kennedy, D. C.
Univ. of Missouri. St. Louis, MO 63121
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5Q(2).
234-239, Coden: JWPFA5 Publ.Yr: Feb. 1978
IIlus refs.
Eng., Fr., Ger., Port., Span, abs.
Languages; ENGLISH
Doc Type: JOURNAL PAPER
Experimental results are presented comparing various methods
for the analysis of simple and complex cyanide In coke plant
wastewaters. Analyses were performed on synthetic solutions
containing various combinations of cyanides (CM-), Fe(CN)6-3,
and SCN-. Additional analyses were performed on actual coking
plant wastewaters with and without standard addition. Simple
and complex cyanides In these wastewaters cannot be reliably
measured by either the Standard Methods or the ASTM procedures
owing to the Interference of sul f ides produced by the
decomposition of thtocyanates during the distillation step. A
simple modifIcatIon is demonstrated to remove sulfIde
Interference by treat Ing the distillate with cadin turn
carbonate. Additionally, the distillation procedure employing
Cu2CI2 as the catalyst Is shown to give consistently lower
results than the magnes1um chloride procedure owing to air
oxidation of Cu+1 to Cu+2 during distillation. A simple
experImental modif teat ton is demonstrated which Increases the
recovery of cyanide when the CU2C12 distillation procedure is
employed, (AM)
Descriptors: Wastewater treatment; Effluent treatment;
Industrial effluents; Coke; Cyanides; Distillation;
analysis
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Congress on Desa!tnatlon
In DESALINATION 22(1-3).
Dec. 1977
wa ter and used
recent municipal
78-O256O
An experience on re-use of waste water discharged from metal
plating shop.
Mural. Y.; Yamadera, T.; Koike. V.
Hitachi Plant Engineering & Construction Co.. Water & Waste
Water Treatment Dlv., Tokyo, Japan
International Congress on Desalination Tokyo. Japan Nov.
27-Dec. 3. 1977
Proceedings of the International
and Water Reuse: Vols. 1 and 2
97-1O4, Coden. DSLNAH Publ.Yr
11 Kis ref s.
No abs.
Languages: ENGLISH
Doc Type- CONFERENCE PAPER
Conventlona) treatment processes for metal plat ing
wastewaters cons 1st of ox Idat ion, reductIon, and
coaguI at ion-sedimentat ion for both r1ns ing
bath. Such treatment does not satIsfy
regulations. A new process treats rinse water, containing the
bulk of cyanide and Cr wastes, with ton exchangers; acid or
alkaline wastewater is treated by chelate resin after
coagulation-sedimentation. The treated water can be returned
to the shop. The mixed bed exchanger consists of a strongly
acid and a weak 1y basic anIon exchange resin after an
activated carbon filter, followed by a strongly basic an*on
exchanger. At the near neutral pH value of the wastewater
made possIbie by this system. complex cyanides are not
precipitated nor cyanide gas produced; free cyanide which
passes the mixed bed exchanger is caught by the strongly basic
exchanger. RegeneratIon water and deterlorated bath are
treated with sodium hypochlortte and ferric sulfate. Chromium
(III) Is treated with other cations with a strongly acid
exchange resin; hydrogen chromate and chromate Ion are treated
with other anions by weakly basic exchange resins. Wastewater
containing heavy metals other than cyanide and Cr is treated
by coagulation and sedimentation, sand filtration, and chelate
resins which adsorb the metals selectively In series. (FT)
Descr iptors: Wastewater treatment; Cyanides; Metal fInishing
Industry wastes; Chromium; Heavy metals; Ion exchange;
Industrial effluents; Resins
Doc Type: CONFERENCE PAPER
At the Swissair Maintenance and Overhaul Base In ZurIch,
wastewater and process effluent treatment Is centralIzed
except for cyanides and chromate plat ing wastes
detoxification. The central treatment for wastewater consists
of clarification stages, neutralization, and sludge treatment
performed by electroflotat ion. Process water treatment.
cons 1st ing of a desalInatIon stage, is performed by RO,
Including necessary pre- and posttreatment equipment. In the
electroflotatIon process, electrolyt leal ly produced minute gas
bubbles which adhere to flocculatIon particles are used to
separate clarIf led water from the sludge phase. Batch
treatment times are 2O-3O min. The sludge layer which forms
on top of the tank Is skImmed pneumatleally at regular
Intervals. In this factitty, electroflotatIon Is laid out in
2 Independent lines with a capacity of 2O m3/hr each. The
out let stream contains J5 ppm SS. Intermediate treatment
cons 1st Ing of post-alum flocculatIon followed by multimedla
pressure filtration, and pH and scale inhibitor conditioning
prepares the stream for RO. Modified cellulose acetate spiral
module membranes are used. Design recovery rate Is 8O% on a
capacity of 720 m3/d. Automatic flushing devices control
membrane fouling. Average salt rejection rates are 98.4%.
Daily plant utilization Is 16 hr-13 hr for waste and 3 hr for
city water. The city water stream has a beneficial effect on
membrane flux performance restoration; the bank flushing
system needs to be used only every 4 wk. Permeate
post treatment Includes degas If teat Ion, pH adjustment, and
carbon bed filtration. Operational costs of the facility are
calculated at about $1.92/t.OOO gal. (FT)
DescrIptors: Swt tzerland; Wastewater treatment; Reverse
osmosis; Flotation; DesalInation; Industrial effluents;
Neutralizat ion; Sludge treatment
Ident 1f iers: electroflotat ton; Swissair; ZurIch
78-O2556
An Integrated Industrial waste water treatment system using
electroflotatIon and reverse osmosis.
Roth. H. P.; Ferguson, P. V.
SwIssair Engineer Ing. Metals Technology Sect ton. Zurich,
Switz.
InternatlonaI Congress on Desalinat ton Tokyo, Japan Nov.
27-Dec. 3, 1977
Proceedings of the International Congress on Desalination
and Water Reuse: Vols. 1 and 2 In DESALINATION 22(1-3).
49-63, Coden: DSLNAH Pub I.Yr• Dec. 1977
i1lus refs
Sum.
Languages ENGLISH
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78-O2439
Cyanide removal from petroleum refinery wastewater using
powdered activated carbon.
Huff. J. E.; Bigger, 0. M.
I IT Research Inst., Chicago. IL 6O6O6
ILLINOIS INSTITUTE FOR ENVIRONMENTAL QUALITY. IIEQ DOCUMENT
Coden: 110002 1OO pp. Publ.Vr: June 1977
I Itus. refs.
Abs.
Languages: ENGLISH
Doc Type; REPORT
A 2-phase program, consisting of batch tests and continuous
tests, was conducted to determine the basic chemistry and
cyanide removal efficiency of the adsorption and catalytic
oxidation of cyanide by powdered activated carbon (PAC) and
cuprlc chloride CuCI2. In the 1st phase, the operating
variables of pH, Cu dosage, mode of Cu addition, C dosage, and
type of C were Investigated. A pH near neutral (pH 6-8.5) was
desirable to obtain low equilibrium cyanide In the aqueous
phase while maintaining a low Cu level. Cyanide removals K95%
were readily achieved In the batch tests using 25O mg/1 of
powdered carbon and I.O-t.S mg/1 Cu on solutions containing
O.5 mg/1 Iron cyanide. The most Important factors In cyanide
removal were the Cu concentration and C concentration In the
solution. Phase II was a series of continuous tests using 2
laboratory-scale activated sludge units and actual refinery
wastewater. Both C and Cu were added to the aeration basin,
and organic removal and cyanide removal performances were
monitored. Cyanide can be successfully removed though the
addition of PAC and CuC12 Into an activated sludge unit. The
biological efficiency did not Indicate any detrimental effects
from the Cu add11 ton (wlth the except Ion of the first test
where the aeration basin was slug-dosed). More C is required
than predicted In the batch tests due to the organ (cs
competing with cyanide for the active sites on the C. This
process requires little or no capital expenditure and should
provide many refineries with an economic approach for reducing
eff tuent cyanide concentratIons. (AM)
Descriptors: Cyanides; Reftnerles; Petroleum industry wastes
; Industrla I effluents; Wastewater treatment; Pollutant
removal; Activated carbon; Copper compounds; Economics
Identifiers- cuprlc chloride; powdered activated carbon
effluents were Na. N, and Cl. Less abundant elements were C.
K, Fe. Ca, Zn. and Mg. Trace quantities of Br„ Mn, Au, Sb,
and Al were also found. Elements usually considered tox1c*Hg.
Pb, cd. and As-were present only In neglIglble amounts.
Organic resistant compounds after Initial carbon treatment
were F6% of the total organic content in secondary effluent.
but Wt/2 of these were adsorbed upon recycling. Most organic
res Is tant compounds were stnal 1 molecules of J24O nm, and
Included chlorinated hydrocarbon, aliphatic acids and salts.
aromatic amines, and phenolic compounds. Major Inorganic
compounds Included Na and Ca chlorides, nitrates, sulfates,
and phosphates. The amount of sI tuple cyanides were
neglIglble. Most of the res 1s tant compounds or the 1r
character 1stIcs found In this study are- in agreement wlth
prevlous ubservations and in general are reasonable. The
compounds classified should give a better understanding of the
res Is tant compounds and serve as a base for fur ther
investigation of their nature. (MS)
DescrIptors: Wastewater treatment; Munlc ipa1 was tes;
Absorption; Activated carbon; Heavy metals; Trace elements;
Organic compounds
IdentIflers: carbon adsorptIon-resistant compounds
78-O1353
Compounds resistant to carbon absorption tn municipal
wastewater treatment.
Chow, 0. K,; Davtd, M. M.
Weyerhaeuser Co.. Tacoma. WA 94BO1
AMERICAN WATER WORKS ASSOCIATION. JOURNAL 69(1O). 555-561
Coden: JAWWA5 Publ Vr: Oct. 1977
1 Ilus. numerous refs.
Sum.
Languages• ENGLISH
Doc Type- JOURNAL PAPER
The most Important elements In compounds resistant to the
carbon adsorpt Ion trea t merit of b lol og lea I and secondary
-------
DIALOG Flle4l: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 47 of 61) User239l3 23Jun82
78-OI275
Physical-chemical treatment of Cleveland district coke plant
waste waters.
Naso, A. c.: John. E. T
Cleveland District Coke Plant
American Iron & Steel Institute 85th General Meeting. New
York. N.V. May 25. 1977
B pp Publ.Yr: { 1977?)
Publ: (n.p.) American Iron and Steel Institute
11lus. refs.
No abs.
Languages: ENGLISH
Reduction of organlcs-pr Inclpal ly phenols, free and
emulsified oils, SS. and cyanides-has been the major problem
In coke plant wastewaters. The sources of this pollution are
excess flushing liquor, barometric condenser water from
crystal sulfate plants, and Intercepting sump water from light
oil plants. Typical contaminant loadings and flow rates from
the above streams In one of the Republic Steel Corporation's
coke plants are tabulated. Discussed are the Investigations
that culminated In the development of a modular system and the
Installation and Initial operation of the organic and phenol
remover, SS and oil removal, and ammonia removal modules of
the system. Organic removal techniques revolved around the
use of activated carbon and were capable of removing organlcs
below a level of O. 1 mg/1, as phenol. Free and emulsified
oils should be removed from the feed waters prior to contact
with the activated carbon. Dissolved gas flotation can
effectively remove SS and free and emulsified oils only If an
anlonlc polyelectrolyte Is added to cause flocculatlon and a
low O2 gas Is used for flotation. Caustic soda Is best for
removing ammonia from crude ammonia liquor, advantages of this
system are listed. Two major process modifications were
necessary. One Involved replacing the barometric condenser
with a surface condenser for cooling the vapors from the
crystal IIzer In the ammonium sulfate plate. The other was the
termination of light oil refining, thus eliminating the
neutral gums and thereby reducing the emulsifIcatIon problem
In the intercepting sump water. The treatment facility was
designed to handle 2 streams, one of 22O gpm and one of 44O
gpm. Characteristics of these 2 streams are listed.
Operational experiences at start-up are discussed and those
areas which presented significant problems are outlined. (SS)
Descriptors: Coke; Ammonia; Industrial effluents; Organic
wastes; Wastewater treatment; Suspended solids; Contaminant
removal; Physlcochemical treatment
Identifiers: phenols; Republic Steel Corp.
78-OO476
"Oxyphotolysls"-process for effluent contaminants.
Harwood. R. H.
Ventron Technology Ltd.
RECYCLING & WASTE DISPOSAL 2(6-7), 156-157.
RWDIDB Publ.Yr. July Aug. 1977
I I lus no ref s
Sum
Languages: ENGLISH
A new broad-spectrum effluent treatment process has recently
been Introduced to the European market This tertiary
treatment process Is capable of meeting projected discharge
limits. Due to the energy Input from UV radiation, the
available oxidation energy per molecule of ozone (O6) is
increased by N35%. The Oxyphotolysis process thus makes more
efficient use of the supplied O6. This process was originally
developed as a treatment method for metal-complexed cyanide
wastes from the electroplating Industry. Chlorinated organlcs
are. for the most part destroyed by the process. Organic
thlophosphorus pesticides, such as malathton, are also
decomposed by the treatment. This process compares favorably
with that using ozone alone, in the decolorizing of unbleached
kraft mill effluent. Treatment of an effluent stream of
I.OOO.OOO gpd would require a dosage of S.OOO Ib/d 06 using O6
alone. With Oxyphotolysis, dosage would be 1,35O Ib/d O6.
The Oxyphotolysis method Is also capable of treating a wide
range of chemical contaminants. (from Text)
Descriptors: Effluents; Wastewater treatment; Engineering;
Ozonation; Cyanides: Metal finishing Industry wastes; Paper
Industry wastes; Tertiary treatment; Chlorinated hydrocarbon
compounds; Pesticides; Photolysis
Identifiers: Oxyphotolysis
77-OS373
Removing soluble metals from uastewater.
METZNER, A.V.
Ecodyne Corp., Industrial Waste Treatment Dlv.
Water & Sewage Works. 124(4): 98-IOt. Apr. 1977 Publ.Yr-
1977
Languages: ENGLISH
Descriptors: ZINC; CHROMIUM: WASTEWATER TREATMENT; COPPER:
TECHNOLOGY: IRON: NICKEL
Identifiers: METAL REMOVAL; CYANIDES
77-O33O8
Evaluation of the toxic effect of CO-2+ and CD(CN) 4-2- Ions
on the growth of mixed mlcroblal population of activated
sludges.
MORQZZI. G.
Universlta DeglI Studl dl Perugia. Facolta di
Science.1st Ituto dl Iglene, Via del Gtochetto. O61OO
Perugia,Ital.
Science of the Total Environment. 7(2): 131-143. Mar.1977
Publ.Yr: 1977
Languages: ENGLISH
Descriptors: WASTEWATER TREATMENT; MICROORGANISMS; CYANIBtS-j
ACTIVATED SLUDGE; GROWTH: TOXICITY: CADMIUM
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DIALOG File41- Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge ScI Abs) (Item 51 of 61) User23913 23JunB2
77-O1457
Wastewater and sludge control in the Canadian metal
finishing Industry: Segment Including chemical, electrolytic
treatment; electrochemical machining and polishing; cyanide
hardening.
BUFFA. L.
Canada Dept. of the Environment, Environmental
ProtectlonServtce, Abatement and Compliance Branch, Ottawa
Ont.KtA OH3, Can.
Canada. Water Pollution Control Directorate.Environmental
Protection Service Report Series. Economtcand Technical Review
Report EPS 3-WP-76-1O. Dec. 1976.46 pp Publ.Vr: 1976
Languages: ENGLISH
Descriptors: METAL FINISHING INDUSTRY WASTES: ECONOMICS:
CANADA; WASTEWATER DISCHARGES; SLUDGES; 'INDUSTRIAL EFFLUENTS
Identifiers- FISHERIES ACT; CONTROL TECHNOLOGY
Descriptors: CYANIDES; INDUSTRIAL EFFLUENTS; METAL INDUSTRY
WASTES; PH; POLLUTION CONTROL EQUIPMENT; WASTEWATER TREATMENT
Identifiers. METAL PLATING BATHS
72-O7743 72-6TF-O1173
Plating and cyanide wastes.
SMITH, STUART E.
Environment/One, Schenectady, NY
Water Pollution Control Federation. Wash., D.C.
Journal.44(6): 11OO - 11O4, June 1972 Publ.Yr: 1972
Languages: ENGLISH
Descriptors: CYANIDE WASTES; METAL FINISHING INDUSTRY;
INDUSTRIAL WASTES; WASTEWATER TREATMENT
Identifiers: 1971; LITERATURE REVIEW; METAL PLATING
LJ
J^
I-1
77-O1344
Detoxification of hardening salts by high pressure steam
treatment (the terra!ysIs process).
SALOMONSSON, G.
Terra Bona AB, Drottnlnggatan 25, 7O2 1O Oerebro, Sweden
Second International Congress on Industrial Wastewaterand
Wastes. Edited by S. H. Jenkins. In Progress In
WaterTechnology, 8(2-3): 163-167, 1976 Publ.Yr: 1976
Languages: ENGLISH
Descriptors: WASTEWATER TREATMENT; BARIUM COMPOUNDS;
CYANIDES; METAL INDUSTRY WASTES
Identifiers: TERRALYSIS PROCESS; HARDENING SALTS
76-O5299
Pollution abatement through the treatment of Industrial
waste water with Ion exchange resins.
WAITZ, W.H. , JR.
Rohm and Haas Co., Pollution Control Research Dept.,
SOOORtchmond St.. Philadelphia. PA 19137
Institute of Environmental Sciences: 22nd AnnualTechnical
Meeting. Mt. Prospect, 111.: Institute ofEnvironmental
Sciences, 1976 pp. 491-495 Publ.Yr: 1976
Languages: ENGLISH
Descriptors: WASTEWATER TREATMENT; RESINS; ECONOMICS;
CYANIDES; METALS; BORON; ION EXCHANGE; INDUSTRIAL EFFLUENTS
Identifiers CHROMATES
72-O6935 72-STI-OO771
Integrated waste water treatment for reusage after cyanide
type plating (3,682,701).
LANCY. LESLIE E.
Ellwood City, PA
Official Gazette. U. S. Patent Office, 9O1(2)•623-624,Aug 8.
1972 Publ.Yr: 1972
Languages: ENGLISH
Descriptors: PATENTS; CYANIDE WASTES; WASTEWATER TREATMENT
Identifiers: ASSIGNOR TO LANCY LABS. INC.. ZELIENOPLE, PA
"72-O2641 72-2TF-OO586
Giving cyanide the treatment.
ANONYMOUS,
UNKNOWN
Chemical Week, I1O(2): 55. 57, Jan. 12. 1972 Publ.Yr: 1972
Languages: ENGLISH
Descriptors: METAL FINISHING INDUSTRY; WASTEWATER TREATMENT;
CYANIDE; TOXIC WASTES
Identifiers: ELECTROPLATING WASTES
76-04259
Instrumentation and automatic control at cyanide waste
treatment.
DIGGENS. A.
Orion Research. Inc.. 380 Putnam Ave.. Cambridge, MA02I39
PollutIon Engineering, 8(3): 43-45, Mar. 1976 Publ.Yr:
1976
Languages ENGLISH
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DIALOG Filed): Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge Scl Abs) (Item SB of 61) User23913 23JunB2
7I-O6822 7I-5TF-O1O68
Elimination of cyanides In the waste waters of the
metallurgical Industry.
MALAFOSSE. J.
L-AIr Llqulde. Lyon, Fr.
See Citation No. 71-5TF-1057. 14 pages. 197O Publ.Yr:
I97O
Languages: ENGLISH
Descriptors WASTEWATER TREATMENT; CYANIDE WASTES: METAL
INDUSTRY
Identifiers: CN ION OXIDATION
71-05413 71-4TF-00660
New process detoxifies cyanide wastes.
MALIN. H. MARTIN. JR.
Environmental Science and Technology, Wash.. DC
Environmental Science and Technology. Wash., D. C.,S(6).
496-497 June 1971 Publ.Yr: 197t
Languages: ENGLISH
Descriptors: CHEMICAL POLLUTANTS; WASTEWATER TREATMENT;
CYANIDE WASTES; OXIDATION
Identifiers: E.I. DU PONT OE NEMOURS; KASTONE PROCESS
7I-O28B4 71-2TF-OO374
Effects of radiation on municipal and Industrial wastewater.
OLESEN, D. E.
Battelle Memorial Inst.. Pacific Northwest Lab.. Waterand
•j£ Waste Management Section, Rlchland, WA
^ See Citation No. 71-2TF-O373 p. 43. 1968 Publ.Yr: 1968
Languages: ENGLISH
Descriptors: RADIATION: PHENOL; CYANIDE WASTES: PETROLEUM
WASTES; MICROORGANISMS; WASTEWATER TREATMENT
Identifiers: ABSTRACT ONLY; RADIATION TREATMENT
7O-O68O7
Removal of organic nitrites from wastewater systems.
LUTIN. PHILIP A.
Hensley-Schmldt, Inc., Chattanooga. TN
See Citation No. P7O-O68OS. pp. 1632-1642, Sept. 197O
Publ.Yr: 197O
Languages: ENGLISH
Descriptors: ACTIVATED SLUDGE: CYANIDE WASTES: OXIDATION;
WASTEWATER TREATMENT
Identifiers: ORGANIC NITRITE REMOVAL
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Print 6/S/I 69
DIALOG Flle4l- Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs > (I tern
I of 69) User 23913 23jun82
U>
*i
Ul
82-O2O5O
Treatment of Metal Containing Hastewater With Calcium
SulfIde
Kim, B.M
GE Co. Schenectady, NY
AlChE Nat. Mtg. Boston, Portland. Chicago 19BO
IN "WATER - I98O VOL. 77. NO. 2O9. pp. 39-48. Publ.Yr:'
19B1
• AICHE. 345 EAST 47 ST.. NEW YORK, NY 1OOI7
SUMMARY LANGUAGE - ENGLISH
Languages- ENGLISH
Recent promulgation of stringent environmental regulations
often requires a process of heavy metals removal more
effective than hydroxide precipitation. Sulflde precipitation
using calcium sulflde slurry was Investigated for cleanup of
heavy metals. Methods for preparing and delivering calcium
sulflde slurry were developed and several processes using such
methods are described. Wastewater samples were treated with
these processes and their applicabilities are presented.
Descriptors: wastewater treatment; heavy metals;
precipitation; water sampling; sulfur compounds; purification
82-O2O49
Precipitation of Heavy Metals With Sodium Sulflde:
Bench-Scale and Full-Scale Experimental Results
Bhattacharyya, D.; Jumawari, A.B.; Sun. G.; Sund-Hagelberg.
C.; Schwltzgebel. K
Dept. Chera. Eng. Univ. KY Lexington, KY 4OSO6
AIChE Nat. Mtg. Boston, Portland, Chicago I98O
IN "WATER - 19BO VOt. 77. NO. 2O9. pp. 3t-38, Publ.Yr:
1981
AICHE. 34S EAST 47 ST.. NEW YORK. NY 1OOI7
SUMMARY LANGUAGE - ENGLISH
Languages: ENGLISH
The results of an extensive Investigation Involving both
laboratory-scale and full-scale sulflde precipitation behavior
of heavy metals and arsenic are presented. The feasibility of
a combination of hydrox Ide-sulf Ide precipitation (at pH 8-9)
process, and a process involving sulflde precipitation (at pH
3-5) followed by lime precipitation. Is established to achieve
a high degree of separation of heavy metals and arsenic from
smelter wastewaters. For precipitation of arsenic and zinc
sulflde at pH < 5. the side reaction between dissolved sulfur
dioxide (If present In wastewater) and sulflde must- be
considered In process design
Descriptors- heavy metals; precipitation; arsenic; sulfur
compounds; separation; wastewater; feasibility studies
1980
IN "I98O NAT. CONF. ENVIRON. ENS. Publ.Yr- 19BO
ASCE, 345 EAST 47TH ST., NEW YORK. N.Y.
Languages: ENGLISH
The objective of this study was to develop an innovative
technology to precipitate and remove toxic metals from
municipal wastewater without simultaneously removing the
largely organic suspended and settleable solids. To achieve
this, an upflow expanded sand bed was used with lime feed to
nucleate precipitation of metals, calcium carbonate and
calcium hydroxylapatIte on the sand grains. This new process
could be. used for pretreatment of municipal wastewater ahead
of conventional treatment to remove heavy metals Into a
relatively small volume of granular precipitate. thus leaving
the primary and secondary wastewater treatment sludges with a
lower metals content and making them more suitable for
agricultural use.
Descriptors: Municipal; Heavy metals; Toxic materials;
Precipitation; Secondary treatment; Wastewater treatment
81-0544t
Comparative Metals Precipitation Techniques
Croy, L.P.; Knocke, W.R.
Dept. Civil Eng.. VA Polytech. Inst. St Univ.. Blacksburg,
VA
19BO Nat. Conf. Environ. Eng. New York, N.Y. dul. 8-IO.
I9BO
IN "I98O NAT. CONF. ENVIRON. ENG. Publ.Yr: I98O
ASCE, 345 EAST 47TH ST.. NEW YORK. N.Y.
Languages: ENGLISH
The treatment of metal-laden electroplating wastewaters has
been through the use of hydroxide precipitation techniques.
This process, somewhat traditional. Is relatively Inexpensive
due to the fact that the main chemical cost relates to the
purchase of lime. However, certain problems have developed
with this method of treatment: (1) ever-tIghtening discharge
standards have begun to exceed the technological capabilities
of hydroxide precipitation; (2) the use of complex Ing agents
In electroplating operation has tended to reduce the
efficiency of hydroxide precipitation systems; and (3) the
resulting metal hydroxide sludges have been shown to be
difficult to thicken and dewater. Thus, It was proposed that
alternate precipitation schemes be Investigated. Patterson et.
al . examined carbonate precipitation of metals and concluded
this process offered no significant benefits In excess of
those obtained with hydroxide precipitation.
Descriptors- Wastewater treatment; Sludge dewatering;
Precipitation; Metals; Economics
8 I-O5586
Pretreatment of Sewage for Heavy Metal Removals
Huang, J -C.; McCole. P.M.
Dept Civ. Eng . Univ. MO, Rol\a
I9BO Nat Conf Environ. Eng New York, N Y. dul .
8- IO,
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DIALOG FHe4l: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc* Abs) (Item 5 of 69) User239l3 23Jun82
flI-O4O25
Filtration for Treating Metal-Finishing Wastes
Yeh. C.H.H.; Ghosh. M.M.
198O Nat. Conf. Environ Eng. New York. N.Y. dul . 8-1O.
19BO
IN "198ONAT. CONF. ENVIRON. ENG." Publ.Yr: 19BO
ASCE. 345 EAST 47TH ST.. NEW YORK, N.Y.
Languages: ENGLISH
The treatment and methods for recovering metals From such
wastes Include chant lea! prectpl tat ton. cementatIon.
electrodeposl tIon. solvent extract Ion, reverse osmosis, and
Ion exchange (1). The selection of a method depends on the
concentration of metals In the wastewater and the ultimate
disposal requirement. In one recovery scheme, the "drag-out"
metals in the voluminous rInse water Is fIrst concentrated
us t ng I on exchange. Then, the concentrated metals In the
regenerat ion back-wash are precipitated and recovered as
hydrated oxides. The process water containing carry over metal
hydroxide floes from the settling and dewatertng steps Is
polished by filtration, thereby making the scheme a totally
"captive" one. Therefore, filtration using either granular
media or precoated septum forms an Integral part of 'this
treatment scheme.
Descr fptors: Industrial wastewaters; Metal fInfshtng
Industry; Wastes; Water pur If leatIon; Filtration
81-O4OI2
Ferrite Process for Treatment of Wastewater Containing Heavy
Metals
IguchI, I.; Kamura. T.; Inoue, M.
Rockwell Internal., Golden. CO Rocky Flats Plant
Publ.Yr: 198O
NTIS. SPRINGFIELD, VA
RFP-Trans-284
Languages: ENGLISH
The ferrlte process as a unique process In the field of
wastewater treatment technology Is Introduced, and the
stabl1IzatIon treatment of electrostat tc precipttator (EP) ash
generated from municipal Incinerators using this process Is
discussed. Informal Ion Is presented on the propertles of
ferrltes, the distribution and concentration of heavy metals
In and the solubility of EP ash, heavy metal leaching, an EP
ash treatment device. and the money savings possible by using
the ferrIte process as compared wl th other stablIIza tIon
methods.
DescrIptors: Wastewater treatment; Heavy metals; Ash;
IncInerators; Leaching; PollutIon dlspersal
198O
IN HI98ONAT. CONF. ENVIRON. ENG." Publ.Yr I98O
ASCE. 345 EAST 47TH ST., NEW YORK, N.Y.
Languages: ENGLISH
The presence of heavy metals In water and wastewater has
been a subject of public concern for several decades. Much has
been publIshed on the adverse effect of heavy metals to
animals and man. In order to safe-guard public health. It Is
essentla I that heavy metals be removed from the aquat1c
environment. The presence of foreign Ions that may modify the
chemical equilibrium picture of the metal solution and thereby
af feet the treatment ef f1cIenty has been essentIa 11y
overlooked. It Is too obvious that complex formation can alter
the chemical characteristics of the metal Ions and affect the
removal mechanisms regardless of the treatment process
employed. It Is therefore the purpose of this study to
Investigate the effect of complex formation on the removal of
heavy metals from water and wastewaters exmpllfled by chemical
precipitation and adsorption processes.
DescrIptors: Heavy metals; Water pollutants; Wastewater
treatment; AdsorptIon; Publ1c health; Ions; PrecIp1tat ion;
Aquat1c environments
81-O39O5
Pretreatment of Sewage for Heavy Metal Removals
Huang. J.-C.; McCole. P.M
Univ. MO. Rolla
198O Nat. Conf. Environ. Eng. New York, N.Y Jul. B-1O.
1980
IN M9BO NAT. CONF. ENVIRON. ENG." Publ.Yr: 198O
ASCE, 345 EAST 47TH ST., NEW YORK, N.Y
Languages: ENGLISH
The objective of this study was to develop an Innovative
technology to precipitate and remove tox fc metals from
municipal wastewater wlthout simultaneously removing the
largely organic suspended and settleable solids. To achieve
this, an upflow expanded sand bed was used with lime feed to
nucleate preclpitat Ion of metals, calcium carbonate and
calcium hydroxylapat1te on the sand grains. This new process
could be used for pretreatment of municipal wastewater ahead
of conventional treatment to remove heavy metals Into a
relatively small volume of granular precipitate, thus leaving
the primary and secondary wastewater treatment sludges with a
lower metals content and makIng them more suI table for
agrleuIturaI use.
DescrIptors: MunlcIpal wastewaters; Heavy metals; Toxic
materlals; PrecIpltat Ion; Wastewater treatment; Secondaiy
treatment
81-O39O6
Effect of Complex Formation on the Removal of Heavy Metals
From Hater and Wastewater
Huang, C.P.; Bowers, A.R.
Dept. Civil Eng., Univ. DE. Newark
19BO Nat. Conf. Environ. Eng. New York. N Y. Jul 8-IO.
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D(ALOG Ftlell Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge Scl Abs) (Item 9 of 69) User239l3 23Jun82
Industrial wastewaters:
LO
*=.
Ul
81-OI797
Foam flotation treatment of
Laboratory and pilot scale.
Wilson, D d. ; Thackston, E. L.
Vanderbllt Univ., Nashville. TN 37235
U.S. Environmental Protection Agency. Office of Research and
Development. Environmental Protection Technology Series
Coden: EPTS8T Publ.Vr: dun I960
11lus. 9O refs.
Abs (Available fromNTIS. Springfield. VA 22161)
Languages: ENGLISH
TREATMENT CODES: D .(DESCRIPTIVE) ; I .(INVESTIGATIVE/OBSER-
VATION)
A floe foam flotation pilot plant removed Pb and Zn In
dilute aqueous solution to quite low concentrations. Design
Improvements are presented. The floe foam flotation of Zn Is
readily carried out with aluminum hydroxide (A1(OH)3) and
sodium lauryl sulfate (NLS). Chromium hydroxide Is floated
with NLS, but adsorbing colloid flotation of Cr+3 with ferric
hydroxide (Fe(OH)3) or AI(OH)3 yielded better results. Cobalt
and Nl levels are reduced to =1 mg/L by flotation with AI(OH)3
and NLS. The Mn*2 levels can be reduced to 1-2 mg/L by
flotation with Fe(OH)3 and NLS. Floe foam flotation of Cu was.
compatible with several precipitation pretreatments (soda ash,
lime, Fe(OH)3, and A1(OH)3), although modifications were
needed to prevent Interference from excessive Ca or CO3-2.
Therefore. floe foam flotation can be used as a polishing
treatment. The flotation of mixtures of Cu*2, Pbt2. and Zn+2
4as conducted using Fe(OH)3 and NLS. The flotation of simple
and complexed cyanides and mixtures of metal cyanide complexes
was also conducted with Fe(OM)3 and NLS; a pH of -5 Is
optimum. A surface adsorption model for floe foam flotation
was analyzed and accounted for the effects of surfactant
concentratIqn, Ionic strength, specifically adsorbed Ions, and
surfactant hydrocarbon chain length. (AM)
Descriptors: Flotation; Industrial wastes; Wastewater
treatment; Pilot plants; Engineering; FlocculatIon; Ions;
Surfactants; Iron compounds; Aluminum compounds; Heavy metals;
Zinc; Nickel; Manganese; Chromium; Cobalt; Copper; Lead;
Chemical treatment: Adsorption
Identifiers: floe foam flotation
wastewaters was evaluated. Five processes were compared in
bench-scale, continuous-flow equ Ipment -convent lonal lime
processing, conventional lime processing plus filtration, lime
with a sulflde polishing and filtration. lime with sulflde,
and lime with sulflde plus filtration. Wastewater samples
from 14 metal working Industries were processed through the
bench-scale equipment using all 5 processes. Reductions In
the concentrations of Cd, Cr. Cu, Nl. and Zn. plus selected
other metals, were measured by atomic absorption chemical
analysis. Capital and operating costs for the processes were
compared for 3 plant slzes-37.85 m3/d (1O.OOO gpd). 757 m3/d
(2OO.OOO gpd). and 1.893 m3/d (5OO.OOO gpd). To reduce the
levels of Cd, Cu. Nl, or Zn from a Wastewater treatment plant
using conventional lime processing. the addition of a final
filtration should be considered first. If filtration does not
achieve the desired low levels, then a sulfide polishing
process with added filtration Is recommended. If reduction of
the levels of Cr, Pb, Ag, or Sn Is required,
lime process plus flltrat >n Is recommended.
process did not significantly reduce the
metals. Details are Included on the use of
electrode for the control of sulflde additions. (AM)
Descriptors: Heavy metals; Precipitation; Wastewater
treatment; Sulfur compounds; Industrial effluents; Lime;
Filtration; Metal Industry wastes; Economics; Engineering;
Cadmium; Copper; Chromium; Nickel; Zinc; Chemical treatment
Identifiers: sulflte precipitation
the conventional
The sulflde
levels of these
specific Ion
BI-O1795
Sulflde precipitation of heavy metals.
Robinson, A. K ; Sum, J. C.
Boeing Commercial Airplane Co.. Manufacturing Research and
Development. P.O. Box 37O7. Seattle, WA 98124
U.S. Environmental Protection Agency. Office of Research and
Development. Environmental Protection Technology Series
Coden: EPTSBF Publ.Vr: dun I98O
1llus. 16 refs.
Abs. (Available fromNTIS. Springfield. VA 2216°))
Languages: ENGLISH
TREATMENT CODES: I .(INVESTIGATIVE/OBSERVATION) D
.(DESCRIPTIVE) : E (ECONOMIC/COMMERCIAL/MARKET)
The sulflde precipitation of heavy metals from Industrial
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DIALOG Flle41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item II of 69) User23913 23JunB2
U)
£*
CTi
An economical answer to
14-16,
One Cul 1 Igan
Coden: INWABK
(CASE STUDY)
reclaiming
and reusing
8I-OI778
Water and uasteuater reclamation:
Industrial wastes and pollution.
Mulvlhtll, J.
Cul I Igan (ISA. Industrial Water Reclamation,
Pkwy.. Northbrook, IL 6OO62
Industrial Wastes 26(4),
Publ.Yr: Jul-Aug 19BO
1 1 lus . no ref s .
No abs .
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: C
.(ECONOMIC/COMMERCIAL/MARKET)
Many companies are economically
heated process water, cooling water. Industrial coolants or
lubricants. wash water and detergents, and demlneral Ized
water. Systems range from SO to 3.OOO gpm. Examples of water
reclamation systems are provided. Including a large truck
terminal In New Jersey, a 120-room motel, a coal processing
plant, a rolling steel mill, a cannery, and a metal conduit
manufacturer. Oxidation, precipitation, and coagulation
properly coupled with physical processes can produce dramatic
and cost effective results. The use of simple sel f -cleaning
screens, cyclone separators. and multimedia and carbon
pressure filters can remove contaminants efficiently. Ion
exchange, membrane/ul tra-f 1 1 trat Ion, and RO processes are
finding more applications In wastewater reclamation systems;
these processes make It possible to filter In the submlcron
range and remove substances classified by molecular weight,
without chemical addition, which can cause problems In a
reclaim environment. The processes for advanced wastewater
treatment gaining the greatest acceptance fall Into the
phys leal -chemical treatment category as opposed to biological
system-,. (FT)
Descriptors: Wastewaters; Water reuse; Economics; Water
pollution control; Contaminant removal; Pollution control
equipment; Wastewater treatment
the following: precipitation, coagulation, and complexatIon:
cementation; electrolytic recovery and electrodlalysls:
solvent extraction; liquid membranes and charged membrane
ultraf11tratIon; RO; ozonatlon; foam separation; Ion exchange;
and evaporative recovery. Miscellaneous treatment methods and
adsorbents, and ultimate disposal are also discussed. (FP.FT)
Descriptors: Heavy metals; Wastewater treatment; Contaminant
removal; Precipitation; Coagulation; Dialysis; Solvent
extraction; Books; Membranes; Filtration; Reverse osmosis;
Ozonatlon; Ion exchange; Evaporation; Waste disposal
Identifiers: state-of-the-art
B1-O1768
Removal of heavy metals from wastewaters.
Beszedlts. S.; Wei, N. S.
B & L Information Services, P.O. Box 45B. Station L,
Toronto, Ontario M6E 2W4, Canada
Publ.Yr: 198O
B & L Information Services
Publ: Toronto. Ontario Canada
IIlus. numerous refs.
No abs. Price: $25.SO
Languages. ENGLISH
Doc Type: BOOK
TREATMENT COOES: D .(DESCRIPTIVE) ; A .(APPLICATIONS) ; M
.(METHODOLOGICAL) ; C .(CASE STUDY)
A state-of-the-art review describes available methods for
the removal, recovery, and disposal of heavy metals, e g.. Cd,
Cu, Fe. Pb. Hg. Mi, Ag, and Zn. Applications of the methods
are 1 J. 1 ysjr_a^ted In case studies. Methods discussed Include
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DIALOG Flle;
Waste treatment; Pollution control; Chemical oxidation;
Kinetics; Economics
Identifiers: rusted tin cans; Cr plating wastes
a I-00759
Utilization of waste tin cans In the control of chromium
plating wastes.
Guano. E. A. R.; Arellano, F-
Ouezon City, Philippines
Second recycling world congress: New and better uses of
secondary resources Manila. Philippines Mar 19-22, 1979
National Science Development Board of the Philippines-Asian
Recycling Association-Bureau International de la
Recuperation-United , Kingdom Society of Chemical
Industry-United Kingdom ''Conservation » Recycl Ing"-Unl ted
Kingdom Institution of Metallurgists-Illinois Institute of
Technology-United States Research Institute-United Kingdom
Institution of Production engineers-Clean Japan Center-Japan
Waste Management Association-United States Bureau of Mines
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DIALOG Mle41- pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 15 of 69) User239l3 23Jun82
CO
8I-OO682
Chemically treating wasteuater: An update.
Qckershausen. R. W.
Bergenfleld, NJ O7621
Water & Sewage Works (Reference Issue). R5I-RS2. RIIO.
Coden: WSWOAC Publ.Vr. Jun I98O
Illus. 4 refs.
Slim.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Many US and Canadian treatment plants use chemical treatment
methods to reduce P In plant effluents. Phosphorus Is
precipitated readily'by Al. fe, and Ca salts resulting In high
SS and BOD reductions. Precipitation reactions are given for
the various salts. A list of wastewater coagulants. and
statistics on P. SS. and BOD reductions using chemical
treatment are given for various treatment plants.
Polyelectrolyte Influence on SS and BOD and points where
addition of the coagulants are most effective are discussed.
The possibilities for removal of potentially harmful metals by
coagulation from drinking water may also be possible. (SS)
Descriptors: Chemical treatment; Wastewater treatment; BOD;
Suspended solids; phosphorus removal; Contaminant removal:
Precipitation; Coagulation; Salts; Metals
Identifiers: polyelectrolytes
B1-OO673
Greenville, Maine-two years later.
Cote, D. R.'
Edward C. Jordan Co.. Inc., 379 Congress St., Portland. ME
O4II1
1979 fall meeting of the New England Water Pollution Control
Association Portland. Maine Oct 22-24. 1979
New England Water Pollution Control Association
New England Water Pollution Control Association. Journal
14(1), S4-6O, Coden: JNEWA6 Publ.Yr: Apt- I98O
I refs.
No abs.
Languages: ENGLISH
Doc Type- JOURNAL PAPER CONFERENCE PAPER
When Greenville, Maine's, advanced wastewater treatment
plant could no longer meet Its discharge permit limitations,
land application was selected as the method of waste disposal.
Effluent from 3 treatment lagoons is pumped to one of two
IB-million gal storage lagoons, which allow for storage during
the winter months. Spray Irrigation to the 160-acre site
takes place during May to Nov. Based on the design flow of
0.17 mgd and a maximum application rate of f.33 tn/wk. = 7O
acres of land are required to handle the waste flow. An
additional 7 acres are required to handle precipitation which
falls on the lagoons. Effluent Is delivered to the Irrigation
system by three 5O-hp centrifugal pumps. To monitor
groundwater quality, monitoring wells are sampled before and
during the spraying season and laboratory analyses are
conducted for pH. N03-. N02-. total Kjeldahl N. total PO4-3,
C1-, specific conductivity, TOC, COD, TDS. and heavy metals.
Results after 1 spray season Indicate a slight lower-Ing of
groundwater pH, a very slight increase In PO4-3, and a small
Increase In N03-. Operational problems during the 1st year
have been minimal. (FT-)
Descriptors: Land application; Wastewater treatment;
Engineering; Biological treatment; Wastewater disposal;
Irrigation; Maine; Water pollution control
Identifiers: Greenville
8I-OO665
Wastewater treatment plant works overtime.
Frltch, G. H.
Howard R. Green Co., Green Engineering Bldg., Cedar Rapids.
IA S24O1
Water and Wastes Engineering 17(9), 7O-73. Coden:
WWAEA2 Publ.Vr: Sep I98O
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The Amana, Iowa, wastewater treatment plant, operated and
maintained by Amana Refrigeration, Inc. (which contributes
>8O% of the design loading), fs described. The plant's
Industrial wastes-containing a high concentration of heavy
metals-arid Its domestic wastes are segregated, with the latter
transported through gravity collector sewers to a pumping
station where It Is ground before being sent to a flow
equalization tank. A concrete splitter box divides the flow
equally to 2 aeration basins. Aerobic digestion Is
accomplished using a center flow mounted mixing system;
treated effluent Is disinfected by chlor Inat ion. Tlie , system
has a hydraulic capacity of 3OO.OOO gpd and an organic
capacity of 5IO Ib of BOOS/d. The segregated waste streams
are pretreated separately. An unusual filtering system then
removes metal hydroxides without prior clarification. The
waste streams are segregated into 2 categorles-Cr+6 wastes and
acid-alkali wastes. Hexavalent chromium Is reduced to Cr+3
with sodium bisulfite under acidic conditions. blended with
the acid-alkali waste, and neutralized to precipitate
Insoluble metal hydroxides. Ferrous sulfate agglomerates the
gelatinous waste, which is filtered through PVC filter tubes.
(FT)
Descriptors: Wastewater treatment plants; Industrial wastes;
Aerobic process; Iowa; Engineering; Biological treatment;
Heavy metals; Domestic wastes; Wastewater treatment
Identifiers: Middle Amana; Amana Refrigeration, Inc .
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DIALOG Flle41: Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge Set Abs) (Item 18 of 69) User239I3 23Jun82
W
*.
(D
8I-OO648
A design study of biochemical combined uasteuater treatment
plant.
Rantala, P.
National Board of Waters, Tampere Water District. Box 297,
SF-33IO1 Tampere to. Finland
Workshop on treatment of domestic and Industrial wastewaters
In large plants Vienna. Austria Sep 3-7. 1979
Internet tonal Association on. Water Pollution Research
Progress in Water Technology 12(3), 271-278. • Coden:
PGWTA2 Publ.yr: 198O
I1lus. no refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER CONFERENCE PAPER
The design study for upgrading the existing chemical
wastewater treatment plant In the city of Tampere (Finland)
was conducted In 1975-78. Various process modifications,
e.g., trickling filters and activated sludge combined with
chemical precipitation, were studied. Almost 1/2 of the
wastewater flow originates from Industry-text Ile, metal, and
paper board mill. Simultaneous ferrous precipitation process
was the most satisfactory treatment method. Laboratory scale
studies showed that paper board mill effluent can easily be
treated together with the municipal wastewater. The paper
board mill wastewater apparently has some good characteristics
In combined treatment. Pilot scale and laboratory scale
studies are also presented. (FT AM)
Descriptors: Precipitation; Wastewater treatment plants;
Engineering; Chemical treatment; F.lnland; Industrial wastes;
Paper Industry wastes; Metal Industry wastes; Textile Industry
wastes
Identifiers: Tampere
methods used to remove heavy metals contaminants from mill
process waters Include solvent extraction. activated carbon,
synthetic polymeric adsorbents. and electrodlalysIs. Should
recovery of the heavy metals from the resultant sludges not be
a cost-effective alternative, the sludges must ultimately be
disposed of at an environmentally safe site. Case histories
are presented which show how some members of the Canadian
mining Industry are meeting pollution control problems at
mining operations. The projects each required a significant
capital commitment and are positive contributions to Improved
environmental quality, (FT)
Descriptors: Canada; Mining; Pollution control;
Environmental protection; Wastewater treatment; Heavy metals;
Contaminant removal; Lime; Mine drainage; Acidic wastes
Identifiers: Brunswick Mining and Smelting Corp. Ltd.;
Hudson Bay Mining and Smelting Co. Ltd.
81-OO577
A glittering future foreseen for the Canadian mining
Industry.
Bhagat, T.
Water S Pollution Control. I45O Don Mills Rd., Don Mills.
Ontario M3B 2X7, Canada
WATER AND POLLUTION CONTROL 118(5), 11-12, Coden.
WPCOAR Publ.Vr: May 198O
11lus. no refs.
No abs.
Languages- ENGLISH
Doc Type: JOURNAL PAPER
The $12 bllIlon/yr- Canadian mining Industry has undertaken a
mul11-bj11 ion dollar development program of new mines,
expansions, and re-openings. Hundreds of millions of dollars
are also being spent on smelter construction. plant
Improvements, and environmental control. An estimated
. $45O-$55O million was spent on environmental control and
Improvement between 1971 and 1975. Treatment techniques
available for removal of heavy metals from mine and mill
wastewaters Include precipitation, cementation. Ion exchange.
charged tnombrane vil traf 11 trat ton. and ozonation. Other
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DIALOG Ft1e41- pollution Abstracts - 7O-82/Apr (Copr, Cambridge Scl Abs) (Item 2O of 69) User239!3 23Jun82
the overland flow (grass
U)
Ln
O
81-OO4B3
Removal of pollutants In
filtration) system.
Scott. T. M.; Fulton, P. M.
Melbourne and Metropolitan Board of Works Farm. Werrlbee,
VIctor ia, Austral la
Developments in land methods of wastewater treatment and
uti1 I sat Ion Melbourne, Austral la Oct 23-27. 4978
International Association on Water Pollution Research-Austr-
alian National Committee of the International Association on
Water Pollut ion Research-Austral Ian Water and Wastewater
Association-International Association of Hydraulic Research~M-
eIbourne and Metropo11 tan Board of Works-UnIver s11 y of
Me Ibourne-Commonwealth Scientific and Industrial Research
QrganlsatIon
PROGRESS IN WATER TECHNOLOGY 11(4-5). 3O1-313. Coden:
PGWTA2 Publ.Yr: 1979
11lus. refs.
Abs.
Languages- ENGLISH
Doc Type- JOURNAL PAPER CONFERENCE PAPER
In the overland flow system at Melbourne, Australia, the
sewage Is given primary sedimentation and passed to Irrigation
areas. A design hydraulic loading on the system of O.23
ML/ha/d can be achieved ' with corresponding BOD5 and SS
loadings of 9O and 4O kg/ha/d. respectively. Both BOD and TOC
decayed In exponential form from mean levels of 5O7 mg/L and
35O mg/L to 24 mg/L and 65 mg/L. respectively. with TOC
approaching a non-decaying residual of 56 mg/L. Suspended
solids reduction was of an exponential nature with a residual
of 22 mg/L. Methylene Blue Acttve Substances showed a similar
decay to levels <1 mg/L. The removal of N was complex and to
some extent unexplaIned. The main N losses could be
attributed to plant uptake and stripping of NH3 from the
wastewater. Organic N loss followed a 1 Inear regression.
Smal1 amounts of NO3- appeared late In the system. The
overa 11 reductIon In N concentrat Ion was 3O%. Little P
removal was evident, with the system exhibiting an apparent
Increase and then a decrease to about the original level.
Precipitation of heavy metals as suI fides In the anaerobic
section of the system was rapid and generally linear with very .
small residuals of unknown organic complexes. The overland
flow system Is effective In the removal of BOOS, SS, and heavy
metals but only moderately efficient In the removal of
nutrients. (AM)
Descr tptors: Pollutant removal; Wastewater treatment; Land
applteat ion; Grasses; N1trogen; phosphorus; Uptake; F11tratIon
; Nutrients; BOD; TOC; Suspended solids
Ident 1flers: overland flow; grass f11tratIon
25NQAA Publ.Yr: 198O
11lus refs.
Sum.
Languages: ENGLISH
Convent ional methods for reducIng Cd concentrat ions in
wastewater Involve neutralization processes using hydroxides
or carbonates followed by separation of the solids by gravity
sedtmentatIon or f M tratIon. On a sroaller scale, su)fIde
precipitation, Ion exchange and neutralization precipitation,
RO, Ion flotat ion, liquid-liquid extraction, electrolysis, and
cementation processes can be used. Electrostatic and cloth
filters and wet scrubbing devices find application In removal
of airborne Cd. To reduce the Cd In dumps. the proportion of
Cd In the refuse must be reduced, the amount of refuse must be
reduced, or Cd-containing products must be produced. Studies
conducted by the Bavarian Industrial Institute have assessed
the efficiency of neutralization and carbonate precipitation
techniques In pure solutions and In effluent samples from an
electroplatIng works. Costs for reducIng Cd emissions in
water and air are also presented. (FT.MS)
Descriptors: Cadmium; Heavy metals; Economics; Air pollution
control; Water pollutIon control; Sedlmentat ion; F11ters;
F11tratIon; Preclpt tat Ion; Ion exchange; Electrochemistry;
Scrubbers; PollutIon control equipment; Sulfur compounds
Identifiers: carbonates; hydroxides
8O-O8496
Methods and costs of preventing cadmium emissions.
Rauhut, A.
Landesgewerbeanstalt Bayern. Nuremberg, Federal Republic of
Germany
COMMISSION OF THE FUROPCAN COMMUNITIES. PUBLICATION Coden:
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DIALOG F1te41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 22 of 69) User239l3 23Jun82
U)
1 cn
8O-O84O3
Toxic control-the trend of the future.
Foess. G. W. ; Ericaon. W. A.
CH2M HILL, 2929 N. May-fair Rd. , Milwaukee. W! 53222
WATER AND WASTES ENGINEERING 17(2). 21-27, Coder-:
WWAEA2 Pub!.Vr: Feb I9SO
11 Jus. refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Federal regulations have been promulgated to control the
quantity of toxics that can be discharged to the public sewers
by Industry and the quantity that can be released by publicly
owned treatment wopks (POTW) to the air, land. and aqueous
environment. On June 26, 1978, EPA publIshed Its regulatory
program governIng Indus trla I dIscharges Into POTW. EPA
published water quality criteria for the 65 priority toxic
pollutants In 1979. On Sept. 13, 1979. EPA published
crIterla for acceptable sol Id waste disposal, Including the
disposal and utilization of wastewater treatment plant sludge.
Air emissions of toxics from POTWs are governed by OSHA air
quality standards and by applicable requirements developed for
state Implementation plans under the Clean Air Act. Virtually
a 1 I municipal wastewaters contain most of the prior I ty
pollutant metals and some of the organlcs. Investigations of
the performance and removal mechanisms of unit processes with
respect to toxics have been performed. Unit processes
discussed Include primary sedlmentatIon, act Ivated sludge,
chemical oxldatIon, chemical preclpltat ion and coagulatIon,
activated carbon adsorption, chelatlon, Ion exchange. RO.
Incineration, and wet-air oxidation. (FT)
DescrIptors: Wastewater treatment; Toxic mater(a)s;
Legislation; Incineration; Sedimentation; Activated sludge;
Oxidation; Chelatlon; Precipitation; Coagulation; Activated
carbon; Ion exchange; Industrial effluents; Sludge disposal;
Po))utant removal; Reverse osmosis; Water quaIt ty acts;
F edera1 regu1a 11ons
Identifiers: Clean Water Act
removed In the ground by preclpltat Ion. While aerobic
conditions in the ground are of special advantage. biological
oxidation of organlcs also occurs under anoxlc conditions If
N03- Is present1. However, organochlorIne compounds are
difficult to remove In the ground If their C1 content Is
excessively high. Other treatment steps have to be used
before or after ground filtration to remove nonbfodegradabIe
organlcs or to alter them Into biodegradable ones. Along the
Rhine River, bank filtration generally removes 75% of the
dissolved organ(cs, and It Is onIy as a result of bank
f11tratIon that later treatment steps Insure a high qua I 1ty
drink Ing water. For this reason, all water utilities In
Germany that rely on surface supplies use ground filtration in
one way or another as part of their treatment scheme. (FT)
Descriptors: Filtration; Rivers; Water treatment; Rhine
River; Contaminant removal; Potable waters; Pollution control;
Fresh waters; FederaI Republie of Germany; Water reuse;
Organic compounds; COD; Organochlorine compounds; Wastewater
treatment
Identifiers: rlverbank filtration
8O-O7627
Experience with rlverbank filtration along the Rhine River.
Sonthelmer, H.
Univ. of Karlsruhe, Engler-Bunte Inst.,
Federal Republ1c of Germany
AMERICAN WATER WORKS ASSOCIATION. JOURNAL
Coden: JAWWA5 publ.Yr- Jul f98O
11lus. refs.
Abs,
Languages. ENGLISH
Doc Type: JOURNAL PAPER
A comparison of dissolved organic chlorine
values found In the Rhine and In bank-filtered water shows a
substantlal reduct ton In the overa11 organic content of the
bank-f11tered water. There Is a nearly constant removal of
=1O mg/L COD and 3.5 mg/L DOC. and removal ts apparently
Independent of the rIver wa ter qua Ii ty. Heavy meta Is can be
0-75OO Karlsruhe.
72(7) , 386-39O,
(DOC) and COD
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DIALOG Flle4l. Pollution Abstracts - 7O-82/Apr (Copr. Cambridge ScI Abs) (Item 24 of 6,9) User23913 23jun82
U>
Ul
U)
BO-O745B
Movement of heavy metals Into » shallow aquifer by leakage
from sewage oxidation ponds.
Nlssenbaum. A.; Wolfberg, A.; Kahanovlch, V.: Avron. M.
Welzmann Inst. of Science, Isotope Dept., Rhovot, Israel
WATER RESEARCH 14(6). 675-679. Coden: UATRAG
Publ.Vr: I98O
(Ilus. refs.
Abs.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
The concentrations of Mn, Nl. Cu. Cd. and Cr were measured
In a shallow perched groundwater aquifer which underlies the
Dan Region Sewage Reclamation Project (Israel). The
contribution of effluents to the groundwaters has been
evaluated on the basis of Cl- concentration. Groundwater
containing >6O% effluents showed a lOO-fold decrease In Cu and
Mn 65O jn away from the ponds. as compared with the near ponds
samples. Nickel and Cd showed only a small decrease In
concentration over ISO m, and then stayed constant. The
concentrations of Cu and particularly of Mn In the
groundwaters near the oxidation ponds Is equivalent to or
greater than in the ponds themselves. Copper and Mn are
mobilized from the precipitated sludge Into the Interstitial
waters. They percolate Into the groundwater near the ponds
and then are precipitated by Increasing aeration during the
movement of the water away from the pond area. Cadmium and Nl
form stable soluble organic chelates which are only slightly
removed by Interaction with the sandy soil of the aquifer. (
AM)
Descriptors: Groundwater; Aquifers; Israel; Effluents; Heavy
metals; Wastewater treatment plants; Sewage; Lagoons;
Activated sludge process: Manganese; Nickel; Copper; Cadmium;
Chromium; Chlorine compounds
Identifiers: Dan Region Sewage Reclamation Project
BO-O6157
Treatment of dilute metal effluents In an electrolytic
preclpltator.
Bryson, A. W.; Dardls. K. A.
Univ. of the Witwatersrand. Dept. of Chemical Eng., Jan
Smuts Ave.. Johannesburg 2OOI, South Africa
WATER S. A 6(2). 85-87. Coden: WASADV Publ.Vr. Apr
I98O
Illus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Excessive concentrations of metals In industrial effluents
may adversely affect the performance of sewage purification
works. Although there Is existing technology for treating
these effluents. it has not found wide application due to
costly equipment and chemicals and the absence of sufficient
space on most plants. The feasibility of removing these
metals from dilute solutions by electrolytic precipitation
using a partlculate electrode Is Investigated A test plant
was constructed which was compact, did not require the
addition of chemicals and could be operated by unskilled
personnel. The plant was Installed at an electroplating works
on the WItwatersrand and was successful in treating wash
waters containing Cu, Nl, Cr, and Zn. (AM) '
Descriptors: Heavy metals; Electric collectors; Industrial
effluents; Wastewater treatment; Nickel; Nickel; Chromium;
Copper; Zinc; Engineering; South Africa: Sewage treatment;
FeaslbllIty studies
Identifiers: Johannesburg: electrolytic preclpltator
8O-O6II6
Bench-scale testing for residual waste treatment.
vuceta. J.; Anderson, J. R.; TeKlppe, R. J.; Calkins, R. J ;
Bishop, W. J.
James M. Montgomery Consulting Engineers. Inc.. 555 £.
Walnut St., Pasadena, CA 9IIOI
5Oth annual conference of the Water Pollution Control
Federation Philadelphia, Pennsylvania Oct 2-7. 1977
Water Pollution Control Federation
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5K1O).
2366-2383, Coden: JWPFA5 Publ.Vr: Oct 1979
Illus. refs.
Eng.. Fr.. Oer., Port., Span. abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER CONFERENCE PAPER
The most effective technologies for centralized treatment of
various Industrial residual wastes generated In Ventura
County, California, were determined. Steps required for a
successful treatment of metallic wastes Include cyanide and
cyanate oxidation, Cr (VI) reduction, hydroxide and sulflde
precipitation, coagulation and flocculation. and filtration.
Ion exchange and carbon sorptlon are not usually required.
Coagulation and flocculation of nonmetaltlc toxic wastes.
followed by filtration and carbon sorptlon. Is more effective
In the removal of toxic nonmetalllc substances from
wastewaters than foam fractlonatIon coupled with carbon
sorptlon. A batch mode of operation is superior to continuous
flow. (AM)
Descriptors: Waste treatment; Filtration; Heavy metals;
Coagulation; Flocculation; Industrial wastes; Wastewater
treatment; Cyanides; California; Oxidation; Precipitation:
Toxic materials
Identifiers, bench-scale testing; Ventura County
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DIALOG Flle4i: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 27 of 69) User239l3 23JunH2
U>
8O-O4673
Hydroxide/modified sulflde precipitation system removes
heavy metals from effluent.
Rogers, K. W ; Wojtklewlcz. J. R.; Marls. J.
Chemical and Environmental Services
CHEMICAL PROCESSING. CHICAGO 42(IO), 32-34, Coden:
CHPCAI Publ.Yr: Sep 1979
I Ilus. no ref s.
No abs.
Languages: ENGLISH
Doc Type. JOURNAL PAPER
A modified method ofjsulflde treatment, where the sulflde
Ion concentration Is easily and Inexpensively controlled so
that the feed matches the sulflde demand of the uastewater. Is
presented. The formation of colloidal precipitates Is avoided
In this treatment for heavy metals In effluent waters. The
modified sulflde process uses an Insoluble sulflde salt, and
Is used In conjunction with standard hydroxide precipitation.
The system functions automatically and requires very little
chemical attention. The cost runs -$2.44/1 .OOO gal of
wastewater. The sys'tem has met EPA requirements, saved water.
reduced the hydraulic load on the municipal system. avoided
municipal user charges, and protected the environment. (FT) •
Descriptors: Heavy metals; Pollutant removal; Effluents;
Wastewater treatment; Sulfur compounds; Precipitation
Identifiers: hydroxIde/sulfIde treatment
8O-O359O
Sludge application: Remove heavy metals two ways.
LewandowskI, G. A.; Abd-EI-Bary, M. F.
New Jersey Inst. of Technology, Newark, NJ O7IO2
WATER & SEWAGE WORKS 127(1), 44-45, Coden: WSWOAC
Publ,Yr: Jan 198O
I Ilus. refs.
No abs
Languages. ENGLISH
Ooc Type: JOURNAL PAPER
To develop agricultural use of municipal sludge as a means
of disposal, methods of removing heavy metals from the sludge
were Investigated. Heavy metals can be eliminated from sludge
at the municipal treatment plant by physlcochemlcal means,
following the primary settler, or treating the combined sludge
prior to digestion. Heavy metals can also be removed at their
source by activated carbon adsorption, adsorption on clay. Ion
exchange, cementation, or electrolysis. The most commonly
used technique Is chemical precipitation as an hydroxide.
carbonate. or sulflde The sequence for heavy metal
precipitation generally Involves equalization, precipitation,
clarification, filtration, and land disposal of the filtered
sludge or metals recovery. Since the volume of Wastewater Is
much smaller at the source than at a receiving municipal
treatment plant, capital and operating costs for heavy metals
removal are less at the source In most cases. The potential
for metals recovery and reuse should be higher at the source
of waste generation, and as disposal costs rise, recovery may
become much more attractive. (FT)
Descriptors: Land application; Sludge disposal; Heavy metals
; Pollutant removal; PhysIcochemicaI treatment; Activated
carbon; Adsorption; Precipitation; Economics
Identifiers: metals recovery
8O-O2682
Management of radlonuclIdes from reprocessing plant gaseous
effluents.
Zabaluev. Y. V.
IAEA. Dlv. of Nuclear Safety and Environmental Protection,
Waste Management Section, Kaerntner Ring II, P.O Box 59O.
lot I Vienna, Austria
INTERNATIONAL ATOMIC ENERGY AGENCY. BULLETIN 21(1), 23-31
Coden: IAEBAB Publ.Yr: Feb 1979
Hlus. refs.
ISSN: 0020-6067
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT COOES: 0 .(DESCRIPTIVE) ; M .(METHODOLOGICAL)
Although current practice at reprocessing plants Is to
discharge most of the gaseous radionuclIdes Into the
environment, methods exist for removing the nuclIdes from the
gas stream prior to discharge. Proposed processes for 85Kr
removal Involve cyrogenlc distillation, fluorocarbon
absorption, adsorption, diffusion, and selective membrane
processes. Liquid scrubbing and sorptlon on solid materials
are 2 alternative methods for trapping 1291 from off-gases.
Options developed for tritium recovery Include volatilization
and collection prior to dissolution, isotroplc enrichment and
collection from liquid effluents. and aqueous recycle with
removal and solIdfIcatIon of a small side stream. For
storage, 85Kr should be encapsulated, preferably embedded In a
metal matrix while 1291 may be held In precipitates from
scrubbing liquids. In Ag molecular sieves and other solid
absorbents, or In charcoal filters Impregnated with doping
agents. Wastewater containing tritium may be stored In sealed
containers prior to disposal, while more concentrated forms of
tritium should be Immobilized In a durable solid. (FT)
Descriptors: Radioactive wastes; Waste management; Krypton;
Iodine; Radio Isptopes; Waste disposal; Nuclear ' fuels;
Radioactive effluents; Gaseous wastes; Hydrogen
Identifiers: fuel reprocessing plants; kr-85; 1-129; removal
processes; tritium
-------
DIALOG Flle41 Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 3O of 69) User23913 23jun82
Ul
Ul
BO-O1928
Methods for neutralizing toxic electroplating
rInseuater-part 3.
Martn, S.; Trattner, R. B.; Cheremlslnoff. P. N.
New Jersey Inst. of Technology, Newark. NJ O71O2
INDUSTRIAL WASTES 25(5). 22-23. Coder! • INWABK
Publ Vr: Sep-Oct 1979
refs.
ISSN. O537-5525
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; D .(DESCRIPTIVE)
In the removal of Cr from electroplating rlnsewater, the
treatment Is Intended to convert Cr+6 to Cr+3. and then to
precipitate It as the Insoluble hydroxide. The reduction Is
performed with sodium bisulfite (NaHS03) at a pH of 2.O. with
the precipitation occurring at pH 8.5, using caustic for the
pH adjustment. A pH recorder-control Ier Is used to measure
the pH and add the NaHSO3 under automatic oxidation-reduction
potential (ORP) control. When the ORP Indicates a value of
3OO mV. the chromates are reduced. and the addition Is
stopped. After 15 mln of mixing, the pH Is adjusted to 8.5,
and after =15 mln of additional stirring, the precipitated
hydroxides are allowed to settle. In the removal of cyanide
and alkali wastes, the cyanides are 1st converted to cyanates
with a 15% solution of sodium hypochlorlte (NaOCI) at a pH
>IO, and are then oxidized to N and CO2 with the NaOCI
solution at pH 8.5. When the ORP reaches a range of 350-40O
mV (Indicating that all cyanides have been oxidized) the
wastewater changes from a clear, transparent green to sky
blue. Complete oxidation takes =IO mln. The treated water Is
allowed to settle for -2 hr, during which time small amounts
of metals, e g., Cu and Ag, will be precipitated as Insoluble
hydroxides (FT)
Descriptors. Industrial wastes; Wastewater treatment;
Chromium; Cyanides: Precipitation; Chemical oxidation;
Reduction; pH; Metals; Toxic materials
Identifiers: electroplating rlnsewaters; automated control;
sodium bisulfite; sodium hypochlorite; hydroxides
Rlnsewaters from the electroplating process contain high
concentrations of cyanides and chromates. To comply with US
EPA discharge standards several chemical processes have been
developed to destroy the cyanides and chromates. For cyanide
the most common form of treatment Is alkaline chlorlnatlon
oxidation by sodium hypochlorlte or C12 plus sodium hydroxide
addition to the waste. Electrolytic decomposition and
ozonatlon are also effective treatments for cyanide wastes.
Chromium waste treatment Involves reduction and precipitation
processes. Reducing agents Include ferrous sulfate. sodium
btsulfate, and sulfur dioxide; neutralizing compounds Include
lime slurry or caustic. Batch treatment Is necessary In shops
having a total dally flow OO.OOO gpd, whereas continuous
treatment Is recommended for volumes >3O,OOO gpd. (FT)
Descriptors: Metal finishing Industry wastes; Cyanides;
Chromium compounds: Wastewater treatment; Contaminant removal;
Chemical oxidation; Neutralization; Reduction
Identifiers: electroplating
toxic electroplating
8O-O1866
Methods for neutralizing
rInsewater-part 1.
Marin. S.; Trattner. R B ; CheremlsInoff. P. N.; Perna, A.
J.
New Jersey Inst. of Technology, Newark, NJ O71O2
INDUSTRIAL WASTES 25(3), 50-52. Coden- INWABK
Publ.Vr. May-Jun 1979
11 Ius. no refs
ISSN 0537-5525
No abs.
Languages ENGLISH
Doc Type. JOURNAL PAPER
TREATMENT CODES: M .(METHODOLOGICAL) ; A .(APPLICATIONS) ; D
(DESCRIPTIVE)
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DIALOG F11e41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 32 of 69) User23913 23Jun82
8O-O1B25
Plant variables determine phosphorus removal methods.
King. P. H ; Haze!wood. R. D.; Tllley. A. R.; Randall. C. W.
Virginia Polytechnic Inst. and State Univ., Dept. of Civil
Eng.. Blacksburg. VA 24O6I
WATER & SEWAGE WORKS Reference Number. R-82-R-86,
Coden: WSWOAC Publ.Yr. 1979
11 Ius. refs.
ISSN: 0043-1125
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES', D .(DESCRIPTIVE) ; M .(METHODOLOGICAL)
Chemical preclpltat Ion methods utilizing time and alum
metal lie salts added prior to pr Imary sedlmentatIon and as
add-on tertiary treatment with mixing and sedimentation are
discussed. The primary and tertiary sludges were generated
after conventional treatment processes and collected after
secondary clarification but before chlorInatton. Lime and
alum were added to separate samples and mixed for 20 and 3O
mtn, respectively. The mixture was allowed to settle 1 hr
before analysis. Phosphorus content was determined by the
vanadomoIybdophosphoric acid colortmetrIc method and total
solids by gravimetric analysis. Sludge dewaterlng properties
were determined by the Buchner funnel specific resistance test
and by gravity drainage In sand drying beds. Primary sludges
had greater dewaterlng properties than tertiary sludges, and
alum sludges, whether primary or -tertiary, were more difficult
to dewater than lime sludges. Optimum mixing time for alum
sludge was 1.5 mln, while for primary lime sludge,, resistance
decreased over a range of mixing times. In tertiary systems,
alum sludge mixing time was optimum after 15 sec, but mixing
time had little effect on lime sludges. Polymer treatment
generally accelerated the gravity drainage phase of sand-bed
dewater ing, whlle air drying rates were unaffected by the
polymer. (FT)
Descriptors: Chemical treatment; Preclpi tat ion; Wastewater
treatment; Sludge dewaterIng; Aluminum compounds; L(me; •
Polymers; Phosphorus removal
metallic ions or both kinds of Ions, depending on the needs of
the operation. Loaded resins are not regenerated in the
electroplating operation but are collected by an operating
company and exchanged for regenerated resins, thereby
eliminating the need to regenerate Ion exchanger resins and to
treat the eluates in a detoxicatlon plant. The essential
sys tern component Is the modu1ar 1on exchanger co1umn with
easI1y replaced cartridges regenerated In a central
Installation when they are charged. The cartridges are easy
to handle and do not require special training for monitoring
and operation. The system can be used for automatic water
recyclIng systems, maintenance of process baths, pre- and
after-treatment baths, separate treatment of rinse baths for
metal recovery, and eltmtnat ton of toxic metals or
complex-forming agents. The Dornter-developed system offers
the following advantages: modular concept Ion, smal1
dimensions, low cost. easy hand!Ing and high operat tonal
safety, and maintenance of prescribed wastewater quality. (
SS.FT)
DescrIptors; • Wastewater treatment; Economics; Metals;
Recycling; Ion exchange; Preclpltat ton; Metal industry;
Technology
XdentIflers: electroplatIng operat ions; modular ion
exchanger column
8O-OO418
RMA-a waste water treatment system for electro-pSating
operations.
Anonymous
Coden: DOPOAC Publ.Vr:
DORNIER POST No. 2. 31-33.
1979
11lus, no refs.
ISSN: OO12-5563
No abs.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
Dornier has developed a cost-effective system for recycling
metals from wastewater which brings wastewater treatment and
metal recycling wlthin the reach of medium and smal^
electroplatIng operat ions . Metals are recycled us Ing high
quant 11 ies of wastewater treated by precIpI tat Ing only
-------
DIALOG FI1e41. Pollution Abstracts - 7O-8?/Apr (Copr. Cambridge ScI Abs) (Item 34 of 69) User239l3 23jun82
U>
U1
79-O4I65
Heavy metal removal with completely nixed anaerobic filter.
DeWalle. F B.; Chian. S. K.; Brush. J.
Univ. of Washington. Dept. of Environmental Health, Seattle.
WA 98IO5
WATER POLLUTION CONTROL FEDERATION. JOURNAL 51(1). 22-36,
Coden. JWPFAS Publ.Vr: Jan. 1979
11lus. refs.
Eng.. Fr., Ger. . Port.. Span, abs.
Languages: ENGLISH
Doc Type- JOURNAL PAPER
A completely mixed anaerobic filter was subjected to various
leachate loadings. At each detention time samples were taken
from the Influent, effluent, and other sampling ports for AAS
heavy metal analysis. The filter was effective In removing
heavy metals. the effectiveness Increasing with Increasing
metal concentrations in the effluent. The metals were
' precipitated as sulftdes, carbonates, and hydroxides and were
removed from the filter as a slurry. With decreasing
hydraulic detention time the metal removal percentage
decreased while the metal content In the bottom slurry
Increased. Most metals were removed In the lower portion of
the filter. Copper was associated with the largest solids
particles, but also showed the largest variation In
concentrations and largest decrease In removal efficiency at
decreasing hydraulic detention times. (AM) T
Descriptors: Copper; Zinc; Nickel; Chromium; Filters;
Anaerobic systems; Heavy metals: Wastewater treatment
Identifiers: metal removal
79-O416O
Influence of pH on purification of zinc-containing solutions
by electrocoagulatIons
Zhurnal Prlkladnol Khtmii. 51(6).1335-1239, June i978
Gnusln. N P.; Vltul'skaya, N. V.; Zabolotskaya. L. I.-, et
al .
Kuban' State Univ.. Uttlsa Sedlna 4, Krasnodar Kraevoj, USSR
JOURNAL OF APPLIED CHEMISTRY OF THE U.S.S.R 51(6).
1187-1189. Coden: JAPUAW Publ.Yr: 1978
11lus. refs. (Some In Russ.)
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The effectiveness of electrocoagulatIon is determined by the
product of the anodic current efficiency, and the coefficient
K. which Is a measure of the tendency of Zn Ions to
coprecIpitat Ion with iron hydroxide. An Investigation Is
reported which was made to determine the quantitative
dependence of these 2 quantities on the solution pH.
Experiments were conducted In a model galvanizing electrolyte
containing 2OO g/L of zinc sulfate, 3O g/L of sodium sulfate.
and 30 g/L of aluminum sulfate diluted with distilled water to
a Zn-ion concentration of 4O mg/L. The solution pH was varied
from 3 to 7 by adding either hydrochloric acid or caustic
soda. Experiments were performed at various current densities
and flowi-ates. The current efficiency was determlnpd from the
amount of Fe dissolved, and the coefficient K from the ratio
of Zn:Fe concentrations in the precipitate. The
Investigations at various Initial pH values Indicated that the
current efficiency depends on both the quantity of
electr Icl ty/unlt volume, and on the solution pll. but that the
coprecfpltat Ion of the 2 metals Is Independent of the pH. (FT
)
Descriptors: Coagulation; Precipitation; Zinc; Iron; pM;
Electrochemistry; Wastewater treatment
Identifiers: electrocoagulation
79-O3I45
Treatmente of base metal mine drainage at pilot scale.
Huck, P. M.; LeClalr, B. P.
CANADA. ENVIRONMENTAL PROTECTION SERVICE REPORT SERIES.
TECHNOLOGY DEVELOPMENT REPORT Coden. TORSDY 94 pp
Publ.Yr. July I97B
11lus. - refs.
Eng.. Fr. abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The suitability of conventional precipitation and
sedimentation techniques to remove Pb, Zn. Cu and Fe from
various types of acid mine drainage in Northeastern New
Brunswick was investigated at pilot scale. A O.3-1.O L/sec
pilot plant was designed for lime and polymer addition.
flocculatIon, clarification, filtration and sludge recycle.
Optimum operating ranges were determined for the Individual
unit processes and data on attainable levels of extractable
and dissolved metals are presented. Experiments were also
conducted to compare two-stage lime neutralization to single
stage neutralization and to Investigate sludge dewaterablI Ity
and effluent toxlcity. Average extractable metal levels
attained as clarlfler overflow concentrations were O.25 mg/L
Pb. O.36 mg/L Zn, O.OS rog/L Cu and O 28 mg/L Fe. Further
reductions were achieved by sand filtration. Dissolved metal
levels in the clarlfler overflow were about equal to
extractable metal levels and were unaffected by further
polishing. No performance were advantages discerned using
two-stage neutralization compared to single stage. Sludge
recycle proved to be an effective technique to Increase
clarlfler sludge density. Sludge dewater Ing tests Indicated
that the sludge could be effectively dewatered by vacuum or
pressure filtration. Bloassay tests showed median lethal
times for salmonid test fish to be consistently In excess of
the 96 hr maximum test period provided that the pH was
adjusted to near neutral values before tests were conducted.
(AH)
Descriptors: Mine drainage; Lead; Zinc; Copper; Iron; Pilot
plants; Wastewater treatment; Canada
Identifiers- New Brunswick
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DIALOG File4l Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 31 of 69) User23913 23jun82
(J\
03
79-O3O64
Methods of estimating sludge from power plant systems.
Kuppusamy, N.
Puerto Rico Water Resource Authority, PR
INDUSTRIAL WASTES 24(3), 32-33. Coden: INWABK
Publ.Yr: May-June 1978
iIlus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Construction and operation of wastewater treatment plants In
power generating station will result If Industry Is to comply
with existing NPOES pemlts. Estimation of the resultant
sludge from such a chemical treatment system will enable an
Industry to preplan a method for handling the sludge. The
sludge obtained by the treatment of continuous wastes can be
computed by assuming a conservative value of I.OOO ppm of TSS
In the original effluent before treatment. The quantity of
dry sludge will be 8.34X10-3 Ib/gal of waste treated, a
negligible amount compared with the sludge obtained due to the
processing of Intermittent waste from air preheater washings,
fan washings, and waterside and fireside cleaning of the
boiler. There Is no hard and fast rule for calculating sludge
amounts from treatment of Intermittent wastes because of their
heavy metal contaminants. To establish a relationship between
the concentration of Fe In the effluent and the resulting
sludge. air preheater wash composite samples were collected
from the cleaning of various units of 4 fossil plants. After
adjusting pH to 8 5 with calcium hydroxide to precipitate
heavy metals, the quantity of resulting sludge was estimated.
The relationship was linear for Fe concentrations up to 2O.OOO
ppm. The same relationship was applicable for sludge
calculation due to treatment of fan washings. Estimation of
the sludge due to the chemical cleaning of the boiler was done
in the same way for all phases of the cleaning except the Cu
removal phase. This curve can be used in conjunction with the
other data to predict sludge quantities. (FT)
Descriptors: Electric power plants; Sludges; Wastewater
treatment plants
79-O3O61
Industrial applications of ozone.
Stopka, K.
U.S Ozonalr Corp.
INDUSTRIAL WASTES 24(3). 23-24. Coden: INWABK
Publ.Yr: May-June 1978
I Ilus. no refs
No abs.
Languages- ENGLISH
Doc Type. JOURNAL PAPER
European and Japanese fisheries use ozone (O3) for
sterilization purposes. Improved treatment of Industrially
contaminated wastewater is obtained by enriching the air used
for oxygenatlon with 5% 03. Sulfurlc acid is added to pH 2-4.
along with .O5-1 g of ferric or aluminum chloride, followed by
alkalIzation to pH 6 5-7.5 with lime. This precipitates most
organlcs. solvents, oils, resins. fatty esters, and toxic
metals. At a retention time of 6-IO mln, 2O mg/L of O3
usually will produce an effluent acceptable to most
environmental requirements. Cyanide decomposition can be
speeded up by as much as 1OO times through Cu catalysis. With
appropriate pretreatment. ozonation of composite wastewater
from a resin manufacturer reduced phenol from 272 to O,
formaIdehyde from 376 to O. and total SS from 2.47O to t6O
mg/L. The COD in acidic wastewater from an edible oil
processing plant was reduced from 1O.5OO to 32O mg/L. a 96%
reduction. For industries requiring ultrapure water. the
treatment system consists of an electrolytic coagulator tank.
a 201 filter, an Ion exchange bed. an O3 system with Tl, O3
concentration from predried air and efficient contactors able
to dissolve Instantly 1 mg/L O3 Into the liquid, and an
activated carbon Filter and O.2I filter on discharge.
Incorporation of an ozonation unit before a RO unit can
prevent membrane clogging. (FT)
Descriptors: Ozonation; Wastewater treatment; Engineering
79-O3O6O
Diesel component plant cuts water consumption with reuse and
recycling.
Anonymous.
INDUSTRIAL WASTES 24(3). 2O-22, Coden: INWABK
Publ.Yr: May-June t978
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
About 9O.OOO GPD of plant wastewater required pretreatment
before discharge Into the sanitary sewer, including 3.OOO gal
of softener regenerants, 3.2OO gat of boiler blowdown. 63.8OO
gal of process rinses. and 2O.OOO gal of oil water from floor
washings, spent coolants, and wash tanks. A batch process Is
used for water treatment. The system Includes four tB.OOO gal
primary holding tanks. Each batch Is treated chemically to
remove oils and precipitate metals as hydroxides. The best
results were obtained when alum was used to coagulate the oil
and lime to neutralize the remaining liquid and precipitate
heavy metals. The alum works even under anaerobic conditions.
The wastewater treatment facility consists of a grit chamber,
a raw waste wet well, 4 batch tanks for waste treatment. a
9.5OO gal storage tank for waste oils. a 9.OOO gal storage
tank for sludge. and 2 outside drying beds. The plant's
average monthly consumption of 16 mgd Is 4O% below the
original estimates, at a savings of about $6.OOO/mo. (FT)
Descriptors: Industrial effluents; Effluent treatment; Water
reuse; Water recycling: Wastewater treatment; Automotive
Industry wastes
Identifiers: dlesel component Industry
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DIALOG FUe4l Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 4O of 69) Usec-23913 23Jun82
CO
Ul
79-O3OOO
Advanced wastewater treatment nature's way.
Ember. L R,
Environmental Science & Technology, 1155 16th St. NW. Wash.,
DC 2OO36
ENVIRONMENTAL SCIENCE & TECHNOLOGY 12(9), IOI3-1O14,
Coden: ESTHAG Publ.Vr: Sept. 1978
i I lus. no ref s. -\
Sum. '
Languages ENGLISH
Doc Type- JOURNAL PAPER
Five interconnected hyacinth ponds, designed to handle a
iOO,OOO-gpd flow and sized for a 6-d maximum retention period,
receIved chlorInated secondary effluent from an actIvated
sludge treatment plant receiving domestic wastes and operating
at 95+% BOD and SS removal efficlences. By Incorporating the
nutrients Into their blomass the plants reduced N levels from
IO-3O to O.6 mg/L, and P levels from 5 to 3.5 mg/L. Harvested
hyacinths can be dried, mixed with sludge, and processed as
fertilizer. or used to produce methane. An alum or ferric
chloride precipitation step may be needed to meet forthcoming
tert iary P standards. The hyacinths reduced the effluent
col I form count to zero and the chlorinated hydrocarbon
concentration to about O.O05 mg/L (5O%): trace metals were
reduced to J O OO1 mg/L. (FT)
Descr tptors: Flor Ida; Wastewater treatment; TertIary
treatment; Phosphorus removal; Nltrogen removal; Col I forms:
ChlorInated hydrocarbon compounds; Plants; Wastewater
treatment plants
Ident if1ers: water hyacinths; Coral SprIngs
and mat er i aI recovery t echn1ques T he mos t prom i s i ng 1nc t ude
evaporative recovery of plating bath constituents from rinse
waters. RO systems for some plating solutions, improved Ion
exchange systems for s ingle metal recovery from separated
rinse streams, secondary polishing systems for final effluent
pur I f lea t ion, r ins-e water pur If 1 cat ion steps pr lor to
evaporative recovery of RO, foreign metal recovery and other
ImpurIty removal From metal f inlshing solutIons,
ultraf111rat Ion methods for water reclamation, and
sol IdIfIcat Ion of metal fInlshlng sludges conta in ing mixed
metal 1Ic hydrox ides. Other promis ing techniques Include
possible utilization of sulflde precipitation of heavy metals.
solvent rIns ing, ion flotat ion, C adsorptIon, and recovery of
metals from hydroxide sludges by solvent extraction. (FT)
Descr iptors: Metal fInlshing Industry; PollutIon control;
Materials recovery; Reverse osmosis; Ion exchange; Engineering
; Cleaning process; Heavy metals; Poland
Identifiers: plating Industry; Polish Institute of Precision
Mechanics
TECHNOLOGY
1978
Plating Effluent Treatment
12(8). 896-899.
79-02832
A clean water project In Poland.
Kleszkowskl, M.; Jackson, G. S.
Inst. of Precision Mechanics,
Dept ¥ OO-967 Warsaw, Pol.
ENVIRONMENTAL SCIENCE &
Coden: ESTHAG Publ.Yr- Aug.
t1lus. refs.
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Wastewaters produced In metal finishing operations contain
such pollutants as cyanides, chromates, heavy metals, mineral
acids, alkal Is. oils, greases, detergents. and organic
sol vents. The most common effluent treatment cons ists of
well-known, conventional chemical procedures which can be done
elther contInuously or batch-wise. They Involve several
opera t i ons. such as a 1ka11ne ch1or Ina t i on of segrega t ed
cyanide solutions, reduction of segregated chromate solutions,
and final neutralization of mixed effluents and precipitation
of metal hydroxides. followed by land fill disposition. A
schemat ic diagram of such an effluent treatment plant Is
presented. Applied research for the Polish metal finishing
Industry Is conducted by the Institute of Precision Mechanics,
In Warsaw, which has developed several new effluent treatments
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DIALOG Ffle41 Pollution Abstracts - 7O~82/Apr (Copr. Cambridge Set Abs > (Item 42 of 69) User239l3 23junB2
CO
CTi
O
79-O259I
Wet electrostatic preclpltator cuts opacity to 10% or less.
Rockenbach. D,
Ferndale. WA 98248
2B-3O,
Coden:
gases from bake
Intalco Aluminum Co.
CHEMICAL PROCESSING. CHICAGO 41(10),
CHPCAI PubI Yr. Sept. 1978
i1lus. no refs.
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The existing scrubber system for exhaust
ovens at a Washington State aluminum plant was not capable of
meeting new air quality codes or wastewater specifications
w t thout add on equipment. Four vert leal wet electros tatIc
precipltators with Integral precondit(oners were chosen
because of their low cost, materials of construction, high
operating velocities, and ease of Installation. Water for the
precfpltator and preconditloner Is treated In separate loops.
No preconditloner loop water is allowed into the precipltator
loop. Hydrated lime Is used for precipitation of F. The
system Is closed loop except for evaporation and the small
amount of IIquor that escapes with the sludge. The wet
prectpltator Is fabricated from corrosion resistant fiberglass
with Hastelloy discharge electrodes. Partlculate efficiencies
during acceptance testing were 9t%~97% with 4 units operating.
Condenslble tars account for t2% of Inlet of 73% of outlet
particulates. for a 67% collection efficiency. The system Is
designed to run In the acid mode while collecting f- but could
be modified to the basic mode to maximize sulfur dioxide
removal. OperatIon is fully automatIc. (FT)
Descriptors- Emission control equipment; Electrostatic
prec Ipitators; Metal 1 ndus try ; A1 urn I nutn; F1 uor 1 des
Iserlohn, and the central treatment plant at He!1Igerthaus are
described. To supplement the system of wastewater treatment
plants 4 impoundments were constructed In the Ruhr valley
The central wastewater treatment plants elimiate 6O% of the
Influent heavy metals. During low flow in the lower Ruhr
river a ratio between clean water and treated wastewater of
7O:3O Is maIntalned on the average. From this mixture
waterworks abstract their water and prepare drinking water by
art IfIcial groundwater recharge. (FT)
DescrIptors: Federal RepublIc of Germany; Metal f inlshlng
Industry wastes; Effluent treatment; Wastewater treatment
plants; Industrlal effluents; MunlcIpal water supplies; Waste
reuse
tdentIflers: Ruhr valley
79-OOG26
Wastewater from plating works-required pretreatment and
disposal of concentrates.
Imhoff. K R.
Ruhrverband und Ruhrtalsperrenvereln, Kronprinzenstrasse 37.
43OO Essen 1, FR6
International conference on advanced treatment of wastewater
Johannesburg, S. Africa June 13-17, 1977
Advanced treatment and reclamation of wastewater: Conference
proceedings. In PROGRESS IN WATER TECHNOLOGY IO(t-2) .
419-43O. Coden: PGWTA2 Publ.Vr: 1978
11lus. refs, (Some in Ger.)
Sum
Languages: ENGLISH
Doc Type. CONFERENCE PAPER
The Ruhrverband ensures that the wastes of metal finishing
establishments In the Ruhr catchment are recycled to the
chemical industry; the sale of the wastes covers onIy
transportation costs, but there are savings compared to
chemical prec1pI tat ton and sludge disposal. Wastewater Is
treated in 118 most\y smalI plants. Cyanide and
chromate-contaIning wastewaters must be collected separately
and pre trea ted. The cen t ra1 decontamIna t i on p1 ant at
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DIALOG Ft)e4t: Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge Scl Abs) (Item 44 of 69) User239l3 23JunB2
U>
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DIALOG Flle4l Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc I Abs) (Item 64 of 69) User23913 23Jun82
7B-OO236
The choice Is yours with phosphorus removal.
Syal, R. K
John David Jones & Assoc., Cuyahoga Falls, OH
WATER AND WASTES ENGINEERING 14(8), 47-5O. Coden:
WWAEA2 Publ.Yr: Aug 1977
11lus no refs.
Sum.
Languages-. ENGLISH
Factors to consider In selecting the most economical method
of P removal from domestic and Industrial wastewaters Include
characteristics of the particular waste. size and type of
basic treatment system, degree of operational and maintenance
attention available, availability and cost of chemicals, and
degree of removal required. Phosphorus In raw wastewater Is
found as orthophosphate fon, polyphosphates or condensed
phosphates, and organic phosphate. Of these, the 1st Is the
easiest to remove by precipitation. Lime and the salts of A1
and Fe are the most commonly used chemicals. The use of lime
Is limited to the primary and tertiary P removal process due
to the tncompatabll Ity of optimum lime precipitation pH
conditions and the maintenance of an optimum environment for
mlcroblal life. Alum or ferrous chloride addition to
activated sludge, or chemical-biological methods, are the most
promising. When planning the system. the designer should be
cognizant of the P levels In the effluent SS. If total P
residuals of JO. 5 mg/t are required, a multimedia filtration
system Is recommended. The advantages of metal addition for
removal are ease of operation, relatively small additional
solids causing Increases In sludge density and dewaterabl1 Ity,
and flexibility to changing conditions. (from Text)
Descriptors: Phosphorus removal; Wastewater treatment;
Aluminum compounds; Iron compounds; Lime
77-OO391
Removal of heavy metals from Industrial effluents.
ROUSE, J.V. ~ •
EPA, National Enforcement Investigations Center, Su1te9OO,
Lincoln Tower. I860 Lincoln St.. Denver. CO 8O2O3
American Society of Civil Engineers. EnvlronmentalEnglneer1 -
ng Division. Journal. 1O2(EE5)- 929-936, Oct.1976 Pub) Yr-
1976
Languages. ENGLISH
Descriptors: INDUSTRIAL EFFLUENTS; HEAVY METALS; ION
EXCHANGE: WASTEWATER TREATMENT; SORPTION; PRECIPITATION;
NEUTRALIZATION; POLLUTANT REMOVAL
Identifiers. REVERSE OSMOSIS: CEMENTATION
Water Research. IO(IO): 9O3-9O7. 1976 Publ.Yr- 1976
Languages: ENGLISH
Descriptors: IRON; PHOSPHATE REMOVAL; ALUMINUM; WASTEWATER
TREATMENT; PRECIPITATION; METALS; COAGULANTS
76-O3343
Heavy-metals recovery promises to pare water-cleanup bills.
Ricci. L.J.
Chemical Engineering, 1221 Avenue of the Americas, NewYork.
NY 1OO2O
Chemical Engineering. 82(27): 29-31. Dec. 22. 1975
Publ.Yr- 1975
Languages: ENGLISH
Descriptors: ADSORPTION; ELECTROCHEMISTRY; ION EXCHANGE;
MATERIALS RECOVERY; METALS; POLLUTION CONTROL EQUIPMENT;
PRECIPITATION; RECYCLING; WASTEWATER TREATMENT
76-O138S
Wastewater treatment at Swedish steel mills.
HALLEN. L.
Vlak AB, Industrial Wastewater Section. Fack, 162
10Vae111ngby, Sweden
Water Pollution Control Federation. Journal, 47(4)-.773-782 .
Apr. 1975 Publ.Yr: 1975
Languages: ENGLISH
Descriptors: FILTRATION; INDUSTRIAL EFFLUENTS; METAL
INDUSTRY; PRECIPITATION; STEEL; SWEDEN: WASTEWATER TREATMENT
Identifiers: MAGNETIC SEPARATION
7B-O4423
Techniques for removing metals from process wastewaters.
OELLINGER, R.W.
Univ. of Maryland. Dept. of Chemical Engineering.
CollegePark. MO 2O742
Chemical Engineering. 81(8): 79-85. Apr. 15. 1974 Publ.Yr:
1974
Languages: ENGLISH
Descriptors: CHEMICAL TREATMENT; ION EXCHANGE; ION REMOVAL;
METALS; POLLUTANT REMOVAL; PRECIPITATION; TRACE ELEMENTS:
WASTE WATER TREATMENT
Identifiers: HEAVY METALS
77-OO229
Comparison of iron(III) and aluminum In precipitation of
phosphate from solution.
HSU. P H.
Rutgers Univ.. Dept of Soils and Crops. New Brunswick.
NJOB903
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to
Print a/5/t-19
DIALOG Fi)e41. Pollution Abstracts - 7O-82/Apr (Copr -CambrIdge ScI Abs) (Item
19) User23913 23jun82
82-OOG22
Local Source Control Program for Metal Finishing Plants
Lo. M.P ; Caballero. R C.; Kremer, J.
Sanitation DIs Los Angeles County,
Waste Sec.
VOL 27, MO. 6.
PP
16-21.
Publ.Yr ;
Indus t.
Whittier, CA
INDUS!. WASTES
1981
Languages ENGLISH
from the experience of the Districts In the past 6 years, a
loca1 source control program has effected a sIgnlfleant
reduction of pollutants from metal finishing companies. Most
have complled with their effluent 11mlts through good
housekeeping measures. Many high production companies have
installed elaborate end-of-pipe treatment systems. Successful
functioning of either type of basic pretreatment system In
dependent upon adequate Involvement of company management In
proper operatIon and maIntenance of the system. Rigorous
enforcement of the Phase I limits by the Sanitation Districts
has encouraged company owners to give close attentIon to
pollution control.
Descriptors: Effluents; PollutIon control; Metal fIntshlng
Industry; DlspersIon; Caltfornla; Water qualIty
81-O1757
Effects of cadmium on the completely mixed activated sludge
process.
Weber. A S.: Sherrard. J. H.
Untv of California, Davis, CA 95616
Water Pot IutJon Control FederatIon.
Journa1
52(9),
2378-2388. Coden: JWPFA5 Pub!,Yr: Sep 198O
11lus 26 refs.
Eng., Fr. , Ger., Port.. Span, abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: I . (INVESUGATS VE/OBSERVAT ION> ; T
.(THEORETICAL/MATHEMATICAL)
A laboratory study was conducted to measure the effect of Cd
on COD removal efficiency, degree of nitrification, and the
kinetic coefficients Ymax (the maximum yield coefficient) and
b (the microorganism maintenance coeff fclent). Data were
obtained from the operation of bench scale reactors which were
fed O. 5.15, and 9.98 mg/L solutions of Cd. Mean cell
residence time was used as the primary operational control
parameter, and values between =3 and 15 d were used to obtain
data. COD removal effIciencies of al1 reactors were
Independent of the mean eel I residence tIme for the range
studied. The COD removal eff Iciencies for the reactors
containing Cd were slightly less than those obtained for the
control reactor. No distinguishable difference was obtained
for the kinetic coefficients Ymax and b. Nttr1fIcatIon,
however, was significantly altered In the presence of Cd The
degree of n1trIf1ca 11on decreased as Cd concentra tIons
Increased at a given mean cell residence time (AM.FT)
Descriptors Cadmium; Activated sludge process; Heavy metals
; Toxlci ty; NltrIfleat ion; COD; Kinetics; Mathemat fcal
analys is;
treatment
Tox ic mater la Is; Laboratory test 1ng
R iolog(ca1
81-OO579
Why Is Rotunda still an RO success?
Suroral1. H.; Schomaker. B
Rotunda West
WATER AND WASTES ENGINEERING 17(7), 24-28. Coden:
WWAEA2 Publ.Yr: Jul 198O
11lus. no refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
A RO water treatment plant In Rotunda West, Florida, In
operation since Jan. 1973, treats SOO.OOO gpd of water, with
the hIghes t IDS va1ue on record. Early prob1ems were
encountered wi th the wel1s pump Ing sand, silt, H2S, and 02.
The problems were corrected by lining the well casing with
PVC.. replacing pump metal He parts, and Installing foot
valves on the suction column below the pumps. The plant has
performed successfully since that time, primarily because of
good operation and maintenance procedures and the use of B-9
hollow fiber membranes. To date, 40 of the original 66
perineators are still In use. Their longevity 1s attributed to
proper and conservat1ve eng ineerIng desIgn and rev lew by
qua 11f i ed per sonneI. (FT)
DescrIptors: Reverse osmosIs; Water treatment plants;
Flor Ida; Membranes
Identifiers: Rotunda West
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DIALOG File4l- Pollution Abstracts - 7O-82/Apr ( Copr Cambridge Sc 1 Abs> (Item 4 of 19) User23913 23JunB2
UJ
-O
OJ
8O-O7062
The economIc 1mpac t of proposed iregu1a 11 cms to reduce
particulate emissions from steel mills and industrial fugitive
sources, R78-10 and R78-11.
ILLINOIS INSTITUTE OF NATURAL RESOURCES IINR DOCUMENT
Pufol Yr• Apr 1979
11lus. numerous refs.
Sum.
Languages: ENGLISH
The benef1ts and costs of the proposals submitted by
Interlake, Inc. and by Granite City Steel are examined.
Quest Ions to be answered concerning the benef1ts of the
regulations Include what reductions In morbidity and mortality
can be expected, what reductions In crop damage and materials
can be expected. and what Improvements In recreation and
aesthetics will result. The question of costs will examine
cap Ital„ operatIon, and maintenance costs as wel1 as the
effect they will have on the price of goods and services of
the producer. Control strategies are evaluated and pollution
sources analyzed. Results of the study are presented, but
their Interpretation ts difficult due to the large amount of
uncertainty associated with the benefits and costs. (AM)
Descriptors: Economics; Cost-benef1t analysis; State
regulatIons; PartIculates; EmlssIon control; Metal Industry;
Air pollutlon control; Environmental Impact; 111(noIs
Ident 1flers• Granlte City Steel; Interlake. Inc.
8O-O2062
Lots of hazardous waste finds a home In Kansas.
Anonymous
NATIONAL WASTE NEWS 2(11), 15-18, Coden NWNED5
Publ.Yr: Nov 1979
11lus. no refs.
No abs
Languages. ENGLISH
Doc Type: JOURNAL PAPER
TREATMENT CODES: C .(CASE STUDY) ; O .(DESCRIPTIVE)
The Kansas Industr tal Environmental ServIces, Incorporated
disposal site Is located In a 90-ft layer of Wellington-Admire
clay beneath which 1s a small nonpotable aquifer The site
began operation fn 1977 and has a life expectancy of 1O-15 yr.
Prior to startup, 1OO permeability studies were conducted on
the 8O-acre site, and 6 perimeter and 4 Internal monitoring
wells were dug to regularly check for leachate. The site
accepts plating wastes, heavy metal slurries and sludges,
concentrated acids, caustIcs, paint sludges, oils and
so1ven t s, cyan Ide compounds, and m1see 11aneous organIc
chemicals Two evaporation lagoons and 4 ponds are used for
evaporation and neutralization of certain wastes, whereas 2
silt trenches and an area fill are employed for landfill Ing
drums. The ftrm Is Involved In a waste stream reduction
program, and the property is landscaped to allow surface water
to drain Into holding and evaporation lagoons. In addition to
a tIght maIntenance program, the f1rm emphasizes safety by
using safety-related equipment and conducting a safe driver
education course (FT)
OescrIptors: Kansas; Disposal sites; Aqui fers; Hazardous
mater la Is; LandfIlls; MaIntenance; Sludge disposal; Acids;
Oils; Solvents; Cyanides; Waste management
Ident Iflers: Kansas Industrla I Environmental Services, Inc.;
permeability studies; safety measures; plating wastes: heavy
metal slurries; caustIcs
8O-O054O
30 years of refuse-fired boiler experience.
Velzy, C. 0.
Charles R Velzy Assoc., Inc , 355 Main St., Armonk, NY
1O504
Engineer Ing FoundatIon conference, uni t operations In
resource recovery engineer Ing RIndge, New Hampshire Jul
1978
RESOURCE RECOVERY AND CONSERVATION 4(1). 83-98, Coden:
RRCODN Publ.Yr: May 1979
tllus refs.
ISSN: O3O4-3967
Abs.
Languages- ENGLISH
Doc Type: JOURNAL PAPER CONFERENCE PAPER
TREATMENT CODES: D .(DESCRIPTIVE)
The town of Hempstead. New York, began operatIng
energy-from-refuse plants In I95O, Incorporating waste heat
boilers and producing power totally Independent of the local
power system. The experiences gained In the areas of boiler
tube metal wastage, boller foul Ing. particulate emission
control, and maintenance and availability are described. With
effective use of overflre air, judicious use of protective
coat Ings, conservat1ve volume and veloclty In the furnace and
convection bank, and limitation of steam temperatures, tube
wastage can be avoided. Careful select Ion of tube
conf iguratIon and spacIng to achieve conservat1ve gas
velocltles along with proper locatIon of sootblowers can
eliminate convection bank tube fouling In incinerator boilers.
Properly cooled walIs along the grate 1Ine shed slag
effectively; however, design of these walls Is critical to
their operation and maintenance experience. A property sized
2-fleld electrostatic predpltator following a well operated
furnace and boiler Is apparently more than adequate to comply
with present federal regulations related to dry partIculates
(AM)
DescrIptors: Refuse disposal; Heat recovery; New York,
Municipal wastes; Resource management; Energy sources; Fuels;
Incinerators; Engineer Ing
IdentIflers: Hempstead
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DIALOG FJle41 Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc* Abs) (Item 7 of 19) User23913 23Jun82
32.5*
water treatment system for electro-plating
No. 2.
31-33.-
Coden: DOPOAC PubI.Y r:
8O-OO418
RMA-a waste
operations.
Anonymous
DORNIER POST
1979
I1 Jus. no refs.
ISSN. OO12-5563
No abs
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Dornier has developed a cost-effective system for recycling
metals from wastewater which brings wastewater treatment and
metal recycling within the reach of medium and smal1
electroplating operations. Metals are recycled using high
quant * tles of wastewater treated by preclpl tat Ing only
metallic Ions or both kinds of tons, depending on the needs of
the operation. Loaded resins are not regenerated In the
electroplating operation but are collected by an operating
company and exchanged for regenerated resins, thereby
eliminating the need to regenerate Ion exchanger resins and to
treat the eluates In a detoxIcatIon plant. The essential
system component Is the modular ion exchanger column wlth
easily replaced cartrIdges regenerated In a central
Installation when they are charged. The cartridges are easy
to handle and do not require special training for monitoring
and operation. The system can be used for automatic water
recycling systems, maintenance of process baths, pre- and
after-treatment baths, separate treatment of rinse baths for
meta 1 recovery, and elImlnatIon of toxIc meta 1s or
complex-forming agents. The Dornier-developed system offers
the following advantages: modular concept Ion, smal1
dimensions, low cost, easy hand!Ing and high operational
safety. and maintenance of prescribed wastewater quality (
SS FT)
Descriptors: Wastewater treatment; Economics; Metals;
RecyclIng; Ion exchange; Preclpltat ton; Metal Industry;
Technology
IdentIflers. electroplating operatIons; modular Ion
exchanger column
and a centrIfugally-operated check valve to assure a positive
shaft seal when shut down. The desIgn provides trouble-free
operation with minimal maintenance. Pumps now In use, each
with a 12-ln suction, a 10-In discharge, and a 21-in Impeller,
are being used to reclrculate solutions of dilute sulfuric
acid (H2S04) and hydrofluoric with a specific gravity of 1.O5
at 145degF and solutions of dilute II2SO4. metallic dust, and
fluorides at 145degF and 134degF (FT)
Oescr iptors: Pumps; Machinery; Engineer Ing; Plastics;
Corrosion; Acids; Smelting; Air pollution control; Pollution
control equipment; Technology
79-O5O96
Packtngless plastic pumps for flow rates to 5,000 gpm.
Anonymous.
CHEMICAL PROCESSING CHICAGO 41(13), 76. Coden: CHPCAI
Publ.Vr: Mid-Nov. 1978
11lus. no refs
No abs.
Languages: ENGLISH
Doc Type JOURNAL PAPER
An acid-resistant, double volute, centrifugal pump, designed
to operate at 5.OOO gpm and heads N18O ft. Is constructed of
modified phenolic resin and carbon-fiber reinforced plastic to
withstand erosion arid corrosive attack by a wide range of
aggressive substances. The pack Ingless design uses and
expelter to create a hydraulic seal when the pump Is running
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DIALOG FUe41 Pollution Abstracts - 7O~82/Apr (Copr. Cambridge Set Abs) < I tern 9 of t9) User23913 23Jun82
79-O4326
A natural environment for resource recovery.
Casterbrook. G, E.
Waste Age, 63tf Gross Point Rd.. Nltes. IL 6O64S
WASTE AGE 9(8). 5O-62, Coden: WAGEAE Pub! , Yr: Aug.
1978
I1lus. no ref s.
Sum.
Languages. ENGLISH
Ooc Type: JOURNAL PAPER
When Monroe County, New York, ran short of landfill space In
the early 1970s and began evaluating new sites, the voters
selected an advanced $5Q.4 million resource recovery plant to
recycle the county wastes The plant designed and scheduled
to be operated by Ray theon Serv ices of CambrIdget
Massachusetts, should start-up early in 1979. Jt was financed
by a $3*.9 million county general-obltgatIons bond and a $18.5
million New Vork State grant from an omnibus bond Issue The
2OOO TPD facility will produce about 65% of the Infeed as RDF.
It 1s also designed to recover ferrous metal. A!, mixed-color
glass, and lesser by-products. The process combined original
Raytheon concepts and materials recovery techniques pioneered
by the BOM. Four shredding stations use a total of 7
shredders. The bulk of the coarse-shredded material wfll
proceed to \ of 4 rotary classifiers, big barrels which turn
slowly while air blows through at 15 or 2O mph. Heavy
materials drop to a conveyor. Light materials reaching the
top of the rotary classifiers will be blown through a fine
screen Into combustible shredders and stored as RDF. The
heavy material Is destined for a more complex treatment-the
separat ton Into residue classes and segregation of the
remaIn Ing RDF stock, The plant also Includes a water
treatment module. Involving a static sieve, filters, and
holding tanks for surges. The multistage shredding operation
should slash maintenance costs, and tne shredder 12 In pass Is
so wide that It wfll not detonate explosives. The RDF will be
transported to Rochester Gas and Electric and used to operate
the recycling plant Itself. The county legislature passed an
ordinance requfrIng all pr1vate refuse haulers to patronize
the plant. (FT)
Descriptors: Solid waste disposal; Materials recover.y; Fuels
; Municipal wastes; New York; Waste management; Waste
treatment plants; Waste recycling
Identifiers: Monroe County; Raytheon Services Co.
PGWTA2
refs.
Publ.Yr 1978
Coden.
illus.
Abs.
Languages- ENGLISH
Doc Type. CONFERENCE PAPER
Water quality monitoring networks should be based on a
flexible modular system of telemetrlc and data processing
modules capable of containing appropriate mathematical models
and deploying only the minimum of robust and reliable sensors
necessary to ach I eve a g 1 ven object I ve . The f o 1 1 ow I ng
sign If leant detertninands are considered: temperature, OO ,
organic matter. SS, C1-, F-, nitrate, ammonia, heavy metals.
trace organlcs, and toxlclty. Sensors should be accurate,
reliable, and require little maintenance. They should be
Interchangeable with others of the same type wt thout
reel ibrat ion. and unaffected by changes In other variables.
They should be Inexpensive, and provide art output easily
connected to the telemetry system Use of dupl Icate sensors
f n a mode such tha t one measures samp I e and the o ther
standard, coupled wl th the abi I ( ty to swl tch streams to
conf irm or deny unusual qua! I ty data , provide automat Ic
calibration, and extend duty cycles, has enabled satisfactory
performance to be achieved from many ex I st ing sensors.
Computers can be used to calculate funct Ions of several
determinants or pollution Indexes so that alarms can be based
on a number of factors taken together. The phys tcochem teal
monitoring scheme In the River Wear uses dual sensors for the
measurement of DO, temperature, turbtdl ty , organic matter , and
ammonia. Opera t Ion of the monl tors Is control led by a
minicomputer at the treatment plant . The dual sensor system
was used to monl tor DO in sett led sewage at Washington
Wastewater Treatment Works. During design, construction, and
commtss toning. It Is advisable to spend effort on staff
training and motivation. (FT)
Descriptors. United Kingdom; Technology; Monitoring systems;
Wastewater treatment plants; Computers; Water quality; Rivers;
Telecommuntcat tons; Monitor Ing Instruments
I dent If lers : telemetry ; sensors
79-OO491
Improvements fn sensor and system technology.
Briggs. R.; Page, H. R. S.; Schofield. J. W.
Water Research Centre, Stevenage Lab., Stevenage,
Hertfordshire SGI ITH, Eng
Internaliona1 workshop on Instrumenta tIon and control for
water and Wastewater treatment and transport systems London
and Stockholm May 1977
Instrumental ion and control for water and Wastewater
treatrnent and transport systems: Internatlonal workshop
proceedings. In PROGRESS IN WATER TECHNOLOGY 9(5-6), 43*52.
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DIALOG Flle4l: Pollution Abstracts - 7O~B2/Apr (Copr Cambridge Scf Abs) (Item II of 19) User23913 23Jun82
Mechanical Engineering. S-22O O7
clean air conference Brisbane, Austral la
78-04157
The expanding role of high ratio fabric filtration In the
metallurgical industries.
Erlesand, 1. ; Stragerk. S,
Lurid Univ. of Technology.
Lund, Sweden
Internat tonal
May 15-19, 1978
Proceedings of the international clean air conference: Clean
alt -the continuing cha Mange. Edited toy E. T. White. P.
Hetherlngton and B. R. Thlele pp. 239-254 Publ.Vr: 1978
Pobl : Ann Arbor, Mich Ann Arbor Science Publishers
i 1 lus . no ref s .
No abs.
Languages: ENGLISH
Doc Type- CONFERENCE PAPER
The experience so far from full-scale Installations with
FLAKT high-ratio filters (HRFs) for cleaning metallurgical
fumes shows that the approach was in the right direction. The
use of HRFs. with filtering velocities somewhat K3 times
larger than with low-ratio filters (LRFs), has decreased the
size of the fabric filter tremendously. The ground space
required is «J5Q% than for the LRF , and the total volume,
estimated from the ground floor to the roof, (s 75% less than
for the LRF. Because of Its smaller size* the HRF has a total
power consumption somewhat less than the LRF. Inspection of
bags taken out after 1 year of operation does not show any
significant wear The cleaning sequence for the FLAKT HRF Is
always control led by the pressure df f ferent (al across the
filter, which minimizes the wearing of the bags. Considering
the advantages for inspection and maintenance, for having fans
downstream of the filter, and the about 2OJ4 lower Investment
cos t , there I s a good chance that In the very near future the
HRF will completely replace the conventional LRF. As further
development is continuing to increase the length of the bags
to 6-7 m and perhaps more, the advantage over LRFs will
stead) ly Increase. (FT)
Descr ip tors . Metal Industry; Industr la I emlss Ions ; Emission
control; Filters; Filter media; Dusts
Identifiers: high-ratio filters; low-ratio filters; FLAKT
aqueous solution obtained from the ore by leaching. Flotation,
or other chetn leal or ptiys leal process , or a h Igh- tempera lure
smelt of fused salts cons 1st Ing of the ore Itself after
SUi table treatment. New methods are tabulated for the
recovery of about 17 metals, and show. In addition to the
extracted metal, the source mater la I„ the method of recovery,
and the developer of the method. In addition, the actual
process Is described In detail. Besides such Incentives as
process stmplIf Icat Ion and by-product recovery, which are
ma Inly geologtca1 In nature, there are technoIog1ca t and
economic advantages to electrochemical metal recovery The
Introduction of electrolytic techniques can reduce the number
of milting operations, avoid complicated chemical procedures,
reduce f ossi1 fuel eonsumpt ion, and make transportation of
voluminous, heavy ore concentrates unnecessary Economic
advantages can be derIved from savings In energy and
mater tals, and redact ton of capital, operat1on, and
maintenance costs, The avoidance of thermal processes
Involving calcination of the ore, decomposition of ore at high
temperatures, emission of flue gases from the fuels used, and
of chemical gaseous species and particutates from the minerals
is invaluable. Wastewaters and other residues or tatHngs In
aqueous solutions are amenable to recovery of the included
metals by electrolysis. The mater ial dispersed to the
environment or going back to the water table can be purified
to meet pollution standards. (FT)
Descriptors: Metals; Metal industry; Mining;
Electrochemlstry; SmeltIng; Economics; Engineer Ing; Mater ials
recovery; Technology; Pollution control; Water purification;
Wastewater treatment
Identifiers: electrolytic metal extraction from ores
78-O397I
Electrochemical recovery of metals.
Barbler, M.
EIectrotechnology: Vol . 1 Wastewater treatment and
separation methods. Edited by R P. Ouellette, J. A. King and
P. N. Cheremlsinoff 239-342 Publ.Vr: 1978
publ: Ann Arbor, Mich. Ann Arbor Science Publishers
11lus numerous refs (Some In Fr,; Ger.)
No abs.
Languages- ENGLISH
Doc Type: BOOK CHAPTER
S tcttus tnforroat ion on current research and deve1opment of
new processes for electrow Inning metals from minera Is is
presented Interest (s focused on methods which have
electrolysis as a common base, the electrolyte being either an
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D1AIOG Flle4l Poilution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 13 of 19) User239l3 23JunB2
-4
78-03453
Viable recycling-fact or fiction.
Dodsworth, M. F.
Council of the Borough of Harrogate* £ng,
SOLID WASTES 68(1). 6-15. Coden: SOWAD3 Publ.Vr:
Jan. 1978
i1lus. no ref s
No abs.
Languages: ENGLISH
Under proper management, recycltng plants can be
economically feasible. About 22O T refuse are processed at
the Harrogate site every week. Large appliances, car parts,
and other easily removable scrap are removed and deposited at
an outside dump area In groups of ferrous and nonferrous
scrap. Glass recyc!Ing proved to be totally uneconomic.
Paper recycling was done using a Scapa Htndte HB4 with a
shredder. Shredding Increased paper bale weights from an
average of 5-6,5 cwt. A separate salvage operation, which has
been In use for a number of years. collects free-of-change
paper and cardboard from commercial premises. During the
domestic collection round. refuse workers place separated
paper on racks fitted to the sides of the collection vehicles.
Tip personnel at the refuse sites receive bonuses based on the
amount of reclaimed paper they separate. Increasing prices of
recycled paper may result In the profitable operation of a
proj ec t In whlch paper f s purchased from voluntary
organizations. The recycling plant at Harrogate produces 2
grades of paper, mixed and ftberboard. Two men could process
N5O T of recycled paper In a normal work week In addition to
routine maintenance and loading trailers. Success of any
recycling scheme Involves minimal labor costs, maximum use of
collection vehicles. and maximum cooperation between workers,
the public, and other various organizations. (FT)
Descriptors: England; Paper wastes; Waste recyclIng; Waste
reuse. Solid wastes; Economics; Scrap metals; Glass
Ident1flers: Harrogate
78-O337O
Electrodlalysfs In advanced waste water treatment.
Korngold. E.; Kock, K.; Strathmann. H.
Bon Gurton Univ., R & D Authority. Beer Sheva, Israel
International symposium on membranes: Desalination and waste
water treatment Jerusalem. Israel Jan. 8-12, 1978
International symposium on membranes: Desalination and waste
water treatment Proceedings. In DESALINATION 24(1-3),
129-139. Coden: DSLNAH Publ.Yr: Jan. 1978
Ulus. ref s.
No abs.
Languages- ENGLISH
Doc Type CONFERENCE PAPER
ETectrodlalysIs (ED) can be successfully applied only to
Industrial effluents with a relatively low salt concentration
which do not contain an excessive amount of organic fouling
nnd poisoning materials. Applicable effluents Include those
produced In t he elect ropIa 11ng. semIconduct or„ and
pharmaceutical industries The advantages of ED over other
treatment processes Include the savIngs on water costs
result ing from complete recyc1 ing of wa ter and vjastewater
cons 11tuents, low Investment costs, contInuous oper at ion at
relatively low energy costs. and automatic operation with a
^minimum of maintenance. The following examples of successful
ED applications are given, regeneration of chemical Cu plating
baths; recyclIng rIns Ing waters from chemical plat ing
processes; recycling electroplating rinsing water; recycling
rIns Ing water from a phosphate plat Ing process; arid recovery
of sulfurIc acid from pickling solutions. (FT)
Oescriptors: Dialysis; Industr lal ef fluents; Eff Kient
treatment; Metal finishing Industry wastes; Waste recycling;
Tertlary treatment
Identifiers: electrodiatysis
78-02305
Arsenic removal from roaster off-gases.
Goodfellow, H. D.; Nennlger, E H.; Twlgge-Molecey. C,; et
al
Can.
Fourth internat tonal clean air conference Tokyo, Japan
May 16-2O. 1977
Fourth international clean air conference: Paper abstracts
p. 195 Publ.Vr: Mar. 15. 1977
Pubi: (n.p ) Japanese Union of Air Pollution Prevention
AssoclatIon
Abs. on t y
Languages; ENGLISH
Doc Type: CONFERENCE PAPER
A system to remove As from a roaster gas was designed in
1972-73 and was commissioned In 1974 for a gold mining
operation In northern Ontario. The gold recovery operation
requires the roasting of arsenical pyrite. The gas system
Includes the removal of entrained dust after the cyclones by a
hot electrostatic preclpltator followed by the sublimation of
arsenic trfoxlde (As2O3) In a unique mixing vessel by direct
contact with Induced ambient air. The mixer Is designed to
maintain the Interface between hot and cold gases away from
the walls and to operate at low energy losses. eliminating
surface butIdup and assocIated maIntenance requirements.
Sublimed As2O3 Is removed in a high-efficiency shaker bag
f H ter before emission from a 1tght-weight. insulated,
metaltIc stack. Operat tng data are presented wt th some
experimental data from the development stage of mixer design.
(AM)
Descriptors: Arsenic compounds; Mining; Canada; Gold;
Gaseous waste treatment; A *r pollutIon control; Pollutant
removal
Ident If1ers' roas ters; arsenic removaI; Ont.; abs tract on I y
-------
DIALOG I-IIall: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Set Afos) (Item 16 of 19) User2331',) 23jun&2
LO
-------
DIALOG Ftle41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge Sc I Abs) (Item 18 oi 19) User239l3 23jun82
78-O1296
A sampler for collecting evolved gases from sediment.
Chau. V. K-: Snodgrass, W J. ; Wong. P. T. S.
Canada Centre for Inland Waters. Burlington, Ont L7R 4A6.
Can.
WATER RESEARCH 11(9), 807-8O9, Coden: WATRAG
Publ. Yr- 1977
11lus. refs.
Abs.
Languages: ENGLISH
A lightweight„ sImple-operatIon sampler was successful1y
applled In studies of the product Ion of methane, carbon
dioxide, N, and O. The sampler Is stainless steel cone 58.5 cm
in diameter and 33-7 cm high. It Is a hand-operated.
sel f -conta fried unl t Gases are col lee ted by water
displacement. The sampler sits on the bottom with the feet
placed away from the gas-evolving area, rather than on thrusts
In the sediment. The sediment tn the sampling area Is exposed
to allow maintenance of natural fauna. The sampler has no
grid bars so the gas evolution Is not caused by mechanical
dIs turbance; Its samp1e bo111e Is de tachab1e 'and can be
replaced In the field. It Is currently used In studies of the
product Ion of volatlie organo-metal1Ic compounds. such as
(CH3)4Pb,
-------
APPENDIX B
METRIC-ENGLISH UNITS CONVERSION
English
1 horsepower (HP)
1 ga lion
1 gallon
1 ft
1 ft2
1 ft3
1 GPD/ft2
1 lb/gallon
1 ft/sec
1 lb
Metric
745.7 Watts
0.0037854 m
3.7854 L
0.3048 m
0.0929 m2
0.0283 m3
0.0407 m3/day/m4
1.20 x 10 mg/L
18.288 m/min
453.59 g.
380
-------
APPENDIX B
REGULATIONS AFFECTING THE
METAL FINISHING INDUSTRY
381
-------
Friday
July 15, 1983
Part ill
Environmental
Protection Agency
Electroplating and Metal Finishing Point
Sourca Categories; Effluent Limitations
Guidelines, Pretreatment Standards, and
New Source- Performance Standards
382
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32482
Federal Register / Vol. 48. No. 137 / Friday, July IS. 1983 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFH Parts 413 and 433
[OW-fflL-2383-7]
Electroplating and A/total Flnisnfng
Point Source Categories; Effluent
Limitations Guidelines, Pretreattnent
Standards, and New Source
Performance Standards
AGSNCY: Environmental Protection.
Agency (EPA).
ACTON: Final rule.
- - JT; Thii regulation limits the
pollutants that electroplating/metal
finishing facilities may discharge to
waters of the United States or to
publicly owned treatment works
(POTW). The Metal Finishing
Regulations provide effluent limitations
baaed on "best practicable technology"
and "best available technology" and
establish new source performance
standards and pretreatment standards
under the Clean Water Act la addition.
this nil? amends the pretreatment
standards for existing sources for the
Electroplating Point Source Category.
The preamble summarizes the legal
authority, background, technical and
economic bases, and other aspects of
the regulation as well as a summary of
comments on the proposed regulation
and on the record supporting ch*
proposed regulation. The abbrevtationsk
acronyms, and other terms used in the
preamble are denned in Appendix A.
(See "Supplementary Information"
befow for complete fable of contentsf.
The Snai ml* i« suppose* by EPA's
technical conclusions detailecLJo the
Development Document forSfftuent
Limitations Guidelines, an&Startthais
far the Metai Frnishinf Point Soots*
Category, June. 1983. The Agency's
economic analysis is found in Economic
Analysis of Effluent Standards and
Limitations for the Metal Finishing
Industry, June 1983. Further supporting
materials are Sled in the record
supporting this rulemaking.
BATES: In accordance, with 40 CFR
100.01 (45 FR 28048} this regulation shall
be considered issued for the purposes of
judlcal review at 1:00 p.m. Eastern time
on July 29,1983. These regulations shall
become effective August 29,1983.
The compliance date for the BAT
regulations is as soon as possible, but no
later than July 1.1984.
The compliance date for New Source
Performance Standards (NSPS] and-
Pretreatment Standards for New
Sources (PSNS) is the date the new
source begins operations. The
compliance date for Metal Finishing
Pretreatment Standards for Existing
Sources (PSES) is February IS, 1986 for
metals and cyanide. Metal Finishing:
PSES establishes two levels of toxic.
organic control: the less stringent must
be met by June 30. 1984 for most plants
and by July 10, 1985 at plants also
subject to Part 420 (Iron and Steellr the
more stringent must be met by February
IS. 1986. In addition. Electroplating PSES
requires toxic organic control by July 15,
1988.
Under Section S09(b)(l) of the Clean.
Water Act judicial review of this
regulation can be obtained only by filing
a petition for review in the United States'
Court of Appeals within 90 day* after
these regulations are considered issued
for the purposes of judicial review. .
Under Section 509(b)(2) oi the Oeaa
Water Act the requirements of the
regulations may not be challenged in
later civil or criminal proceedings
brought by EPA to enforce these.
requirements.
Reporting provisions' in 40 CFR 413.03-
and 433.12 will be reviewed by OMB
under the paperwork reduction act and
are not effective- until approved.
Aoomss: Tecamcal information may be
obtained by .writing to Mr. Richard.
Kincifc. Effluent Guidelines Division
(WH-552), Environmental Protection
Agency, 401 M St. S.W, Washington.
D.C. 20480, Attention: Metal Finishing
Rule* Approximately two weeks faaa
publication, to* record for this
rulemaking will be available for
"aaaectioa and* copying at the EPA •
Public Information Reference Unit.
Room-240* {Rearf PM-213 (EPA Libraryji
The EBA pdtticisfonnation reguiaooB
(40 CFR Part 2f onvides that a
reasonable-fee1 may be charged for •
sopging. Copies, of. the technical and
economic, documents may be obtained
Sum the. National- Technical Information
Service. Springfield. Virginia 22I8I (703/
487-4850). Copies of both document*
will be available for review In me public'
record at EPA headquarters and
regional libraries.
Mr. Richard Kinch. Effluent Guidelines
Division (WH-332), EPA. 401 M Street.
S.W., Washington. D.C 20460. or by
calling (202) 382-7159. Economic
information may be obtained by writing
Ms. Kathleen Ehrensberger. Economics
Branch (WH-586), Environmental
Protection Agency, 401 M St. S.W.,
Washington. D.C 20480. or by Bailing
(202) 382-5397.
3UPKEMINTAHY INFORMATION:
Organization of This Nonca-
!. Legal Authority
II. Background
•*. The Claan Water Act
3. Pnor EPA Regulations
C Overview of the Industry
JE. Scope of this Rulemaking
[V. Data Gathering Efforts
V. Sampling and Analytical-Program
VI. Industry Subcategonzation
Vtt, Available Wastewater Control and
Treatment Technology
A. Status ot In-Ptacs Technology
3-. Control Treatment Options
vnt Ganeral Criteria tor Lumtations
A. 3PT Effluent Limitations
3. BAT Effluent Limitations •
C 3CT Effluent Limitations
C 3CT Effluent Limitations
0. New Source Performance Standards
E. Pretreatment Standards for Existing
Sooreas
f. Rretreaanent Standards foi>New Sources
DC Summary of Final Regulations
. A. Pan 433
3: Pan 413
X,Qenvaaon of the Limitations
XL Changes from the Proposed Limits
XHL Pollutants and Subcategones Not
Regulated
A. Exclusionjjf Toxic Pollutants
E Exclusion of Subcategones
Xffi Costs. Effluent Reduction Benefits, and
Economic Impacts
A. Costs and Economic Impacts
3. Executive Order 12231
C Regulatory Flexibility Analysis
O.SBA Loans
XIV. Non-Water-Quality Environmental
Impacts
A. Air Pollution
a Noise
C Radiation
aSbfidWaste
E,So«tgy
XV. Best Management Practices (BMPsI
XVL C/pMt and Bypass Provisions
XVTL Variances and Modifications
XVm. Implementation of Limitations and
Standards
' A. Relation to NPDES Permits
3. Indirect Dischargers
C. Applicability and Compliance Dates
0. Enforcement
XIX Summary of Public Participation
XX. Availability oi Technical Information
XXL OMB Review
XXH. List of Subjects
XXm Appendices
A. Abbreviations. Acronyms, and Other
Terms Used in This Notice
3'. Pollutants Excluded From Regulation
C, Unit Operations in the Metai Finishing
Industry
L. Legal Authority
This regulation is being- promulgated
under the authority of Sections 301. 304.
306.307, 308. and 501 of the Clean Water
Act (the Federal Water Pollution Control
Act Amendments of 1972. 33 U.S.C. 12S1
etseq.. as amended by the Clean Water
Act of 1977, Pub. L. 95-217) (the "Act")
and as further amended. This regulation
is also being promulgated in response to
the Settlement Agreement in Natural
Resources Defense Council. Inc. v
383
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Federal Register / Vol. 48. No. 137 / Friday. July 15. 1983 / Rules and Regulations 32463
Train. 8 ERC 2120 (D.D.C 1978), as
modified. 12 ERC 1333 (D.D.C. 1973).
modified by Order dated October 28.
1962.
tt, Background
A. The Clean Water Act
The Federal Water Pollution Control
Act Amendments of 1972 established a
comprehensive program to "restore and
maintain the chemical, physical, and
biological integrity of the Nation's
waters," Section 101(a).
• Section 301(b)(l)(A) set a deadline
of July 1.1977. for existing industrial
direct dischargers to achieve "effluent
limitations requiring the application of
the best practicable control technology
currently avaiiable" ("BPT"].
• Section 301(b)(2)(A) set a deadline
of July 1.1983. for those dischargers to
achieve "effluent limitations requiring
the application of the best available
technology economically achievable...
which will result in reasonable further
progress toward the national goal of
eliminating the discharge of all
pollutants" ("BAT1).
• Section 306 required that new •
industrial direct dischargers comply
with new source performance standards
("NSPS"), based on best available
demonstrated technology.
• Sections 307 (b) and (c) required
pretreatmerit standards for new and
existing dischargers to publicly owned
treatment works f^'POTW"]. The Act
made pntnatment standards
enforceable directly against dischargers
to POTWs (indirect dischargers), unlike
the requirements for direct dischargers
which were to be incorporated into
National Pollutant Discharge
Elimination System (NPDES) permits
issued under Section 402.
• Section 402(a)(l) allows
requirements for direct dischargers to be
set case-by-case. However, Congress
intended control requirements to be
based for the most part on regulations
promulgated by the Administrator of
EPA.
• Section 304(b) required regulations
that establish effluent limitations
reflecting the ability of BPT and BAT to
reduce .effluent discharge.
• Sections 304(c) and 308 of the Act
required regulations for NSPS.
• Sections 304(g), 307(b), and 307(c)
required regulations for pretreatment
standards.
• In addition to these regulations for
designated industry categories. Section
307(a) required the Administrator to
promulgate effluent standards
applicable to all dischargers of toxic
pollutants.
• Section 308 gave the Administrator
authority to collect information
necessary to develop and enforce
regulations.
• Finally, Section 50l(a) authorized
the Administrator to prescribe any
additional regulations "necessary to
carry out his functions" under the Act
EPA was unable to promulgate many
of these regulations by the deadlines
contained in the Act and as a result—in
1978. EPA was sued by several
environmental groups. In settling this
lawsuit EPA and the plaintiffs executed
a "Settlement Agreement" which was
approved by the Court This agreement
required EPA to develop a program and
meet a schedule for controlling 65
"priority" pollutants and classes of
pollutants. In carrying out this program
EPA must promulgate BAT effluent
limitations guidelines,-pretreatment
standards-and new source performance
standards for 21 major industries. See
Natural Sesouceas Defense Council Inc.
v. Train. 3 ERC 2120 (DJ3.C. 1978),
modified. 12ERC 1333 (D.D.C. 1979).
modified by Order dated October 28,
1982.
Several of the basic elements of the
Settlement Agreement program wen
incorporated into the Claan Water Act
of 1977. This law also makes several
other important changes in the Federal
water pollution control program.
• Sections 301(b)(2)(A) and
301(b)(2!(Q of the Act now set July 1. -
1984 as the deadline for industries to
achieve effluent limitations requiring
application of BAT for "toxic"
pollutants. 'Toxic" pollutants hen
includes the 65 "priority" pollutants and
classes of pollutants which Congress
declared "toxic" under Section 307(aj of
the Act \ ->
• Likewise. EPA's programs for new
source performance standards and
pretreatment standards an now aimed
principally at controlling toxic
pollutants.
• To strengthen the toxics-control
program. Section 304(e) of the Act
. authorizes the Administrator to
prescribe certain "best management
practices" ("BMPs"]. These BMPs are to
prevent the release of toxic and
hazardous pollutants from: (1) Plant site
runoff, (2) spillage or leaks. (3) sludge or
waste disposal, and (4) drainage from
raw material storage if any of those
events are associated with, or ancillary
to. the manufacturing or treatment
process.
In keeping with its emphasis on toxic
pollutants, the Clean Water Act of 1977
also revises the control program for non-
toxic pollutants.
• For "conventional" pollutants
identified under Section 304(a){4)
(including biochemical oxygen demand.
suspended solids, fecal coliform and
pH), the new Section 301(b)(2)(E)
requires "effluent limitations requiring
the application of the best conventional
pollutant control technology" ("BCT"}—
Instead of. BAT—
-------
32464
Federal Register / VoL 48. Mo. 137 / Friday, July 15. 1983 / Rules and Regulations
several metal finishing operations other
than, and in addition to. electroplating.
Part 413 (electroplating) currently
applies only to flows from, the six
specified electroplating processes.
These Part 433 (metai mushing
regulations} will apply- to- those
electroplating streams and also' to-
wastestreams from most other metai
finishing operations, within the same
plants. Tha Fart 433 PSES will apply
only to plants, already covered by Part
41% however Pact 433* will often cover
additional wastewater within the same.
plants-Tims the Part 433, limits, on
discharge o£ toxic metals* toxic, organics.
and cyanide wuXanply M "VM^ faraliHtt^
in the elacttopiatihg/metal finishing,
industry. ' '
The industry cantoe. divided '""*" t&a
sectors indicated: oa Table L FaoEBaa.
are either "captives'.* [those which in. a,
calendar year own more tfiaaSOSS (ana
basis) of the materials undergoing metal
R i u'ufn'n^fe nr ~fyfy shops" CtSOSe w.nich
in a" calendar year do oat awnmortt ffrQ«i
50% fares' basisf of material undergoing
Captrres- can be farther divided by
two. definitional "integrated" piano are-
those which, prior to treatment combine
electroplating waste streams witfc
significant process1 wast? streams' not
covered hytheeiei.Quy/affuj category
"non-integrated** faotitfes are tftose
which have significant wastewater-'
discharges only from* operations.
addressed by the* eteulruplu1 ting
category. Many captives.~(5WTare
"integrateo?* facilities: Whereas captives
often have a complex range of"
operations* job shops' tonally perform*
fewer operations. In-theory job shops
can be divided like- captive*, in-
actuality, however, approximately 97^
of all job' shops ia this industry are
"non-integrated".
Finally, the- entire industry can- be
divided inWdirecf and "Indirect"
dischargers; "Directs/* discharge
wastewaters to waters' of the United
States and-are snbfect toNPDES permits
incorporating BFT. BAT. and BC7
limitations or NSPS." "Indirects"
discharge to- POTWs and are subiect (o
PSESorPSNS.
As. discussed above, the
electroplating/metal fiaiahuig. industry is
currently covered by Part 413 PSES Cor
the Electroplating Category promulgated
on, September 7.1373. and amended on
January 23,1981. The effect of today's
amendments- is to create a new
category—Metal Finishing (Part 433}—
and to shift most eiectroplaters to it
replacing their current PSES with new
limits which apply uniformly to
discharges from their electroplating and
other metai finishing operations. This
meets industry's requests for equivalent
limits for process- lines often found
together and greatly reduces the need to
rely on the Combined Waste Stream
Formula for integrated metal- finishing
facilities. Direct discharger and new
source- requirements are- also being:
regulations.
Indirect discharging' job shop1
eiectroplatersand independent printed
circuit board manufacturers however.
would be left tinder the existing Part 413
PSES for Electroplating and are- -
exempted from- Part 432 This ia
consistent with-»1980 Settlement
Agreement in wnicir the Nafionaf
Association1 of Metal Finishers- (NAMFJ,
and the* ins finite* for* strercofflteutJJitf. and
Packaging: Electronic Orcnits (UPEC?
agreed nof to cnaileng»tne> Parr 443
PSES h* fBC&xst Sot tus*198X aiueiiumefl ts
and9 2?^^ CDmmxtm&m* tnaC tns Agency
more stringent standards fartfiose'
TASC* fc—3»ej«oowi»orTHe'
&ecrmPUkTiNa/MerM..BN(siHiNa INOUSTMT
CNunav <* QMMI a* xonr 11*701
would apply to discharges from the
second operation.
The following, regulations will take
precedence over metal finishing (Part
433) and electroplating (Part 413) wnen
such an overlap occurs:
Nonferrous metal smelting and refining
(4OCER'Part 421)
Coil coating (40 CFR Part 465)
Porcelain enameling (40 CFR- Part 486)
Battery manufacturing (40 CFR Part 481)
Iron and steel (40 CFR Part 420J
Metal casting foundries (40 CFR Part
484).
Aluminum forming (40 CFR Part 467)
Copper forming (40 CFR Part 466)
Plastic-molding1 and forming (40 CFR
Part483r
In. addition. EFA is. excluding, from the
nrstai ftaisaing.fPart 433) regulation: (1)
Metallfc'piatamakmg.and gravure
cyUnderpreparanon conducted witftin
printing- and. publishing facilities: and (2)
existing source fob shops and
"independent•prnrted circuit board
manufacturers which introduce
pollutants'into a publicly owned
treatment works. As-noted above, the
standards' do- not apply to facilities
unless they perform- at feast one of the
foilowingr electroplating, eiectroless,
plating; anododng,. coating* chemical
etching and ""iifttg? or printed circuit
Tie- Metal FSrisning, Category covers-
plants which perform one or more o£ the
following six operations: electroplating.
electroless. plating, anodizing, coating \
[phoapnaongr ^^^«i»Hffgl amj coloong).
chemical atrhin^ qiftH
circuit board manufactnre. If a plant
performs any of. taom six operations
then discharges- from the 4ft operations
listed in Appendix C are*cov«red-by
these standards.
In. some cases, another industrial
category may cover wastawster
dischazgea frum a. mntaJ fimahma
operation. In such, cases, the more
specific standards of the other Part(a}
will apply to toose- waatewater streams
which, appear to- bs covered by both.
regulation*, rot axampia, if a plant
performs coating operations in
preparation for painting and also
performs electroless plating as part of a
porcelain enamellng-procass* then these
Part 433 standards would apply to
discharges from the coating operation:
while Part 486 (porcelain enameling)
Tne most important pollutants of
GODC8T9 lOUQu jfl fflBtST SD2SIUI3S
indnstry wastewatersjre: (1) toxic
nretals (cadmnmt* copper, chromium.
nickel, lead, and ancjr (2) cyanide: (3)
'toxurorgaaics (lumped together as total
toxic organies); and (4) conventional
pollutants-(TSS and oil and grease).
These and other chemical constituents
degrade water quality, endanger aquatic
life and human health, and in addition
corrode equipment generate hazardous
gas, and cause treatment plant
malfunctions and problems in disposing
of sludges containing toxic metala.
These plants manufacture a variety of
product! that are* constructed primarily
of metals. The operations, which involve
materials that begin as raw stock (rods.
ban. sheet castings, forgmgs. etc-),' can
include the most sophisticated surface
finishing technologies.-These facilities
include both captives and job shops.
They vary greatly, in size. age. number of
employees, and number and type of
operations performed. They range from
very small job shops with less than 10
employees to Urge facilities employing
thousands of production workers.
Because of differences in size and
processes, production facilities are
custom-tailored to the individual plant.
Some complex products may require the
385
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Federal Rebate? / Vol. 48. Na. 137 / Friday, July 15. 1983 / Rules and Regulations 32485
use of nearly all of the 46 unit operations
metioned above; a simple product may
require only one.
Many different raw materials are used
by these plants. Basis materials (or
"workplaces") -are mostly metals; from
common copper and steel to extremely
expensive high-grade alloys and
precious metals. They can also include
plastics. Solutions used in unit
operations can contain acids, bases,
cyanide, metals, completing agents.
organic additives, oils, and detergents.
All these materials may enter waste'
streams during production. - -
Water use within, the metal finishing
industry-is discussed fully in Section V
of the development document (see
summary above). Plating and cleaning
operations are-typically the biggest
water users. While moat matai finishing
operations ose-water, some may use
none at all Water use depends heavily
on the type—and the flaw rate—of the
rinsing used. Product quality
requirements often dictate me. amount of
rinsing needed for specific parts. Parts
involving extensive surface preparation
will generally require larger amounts of
water in rinsing.
10. Scope of tfr"« Ruieznaking
This regulation establishes Pan 433-
3PT, BAT, NSPS. PSE& and PSNS for
the Metal Finishing Pauit Source-
Category and amends Part 413.PSES for
the Electroplating Point Sonrce
Category. The BAT goal is to achieve, by
July 1,1984. the beat available
technology economically achievable
that will result in reasonable further
progress toward the national goal of
eliminating the discharge of all
pollutants. This regulation does not alter
the existing metal and cyanide
standards for job shop electroplaters
and printed circuit board manufacturers
discharging to POTWs.
EPA first studied the electroplating/
metal finishing industry to determine
whether differences in-raw materials.
final products, manufacturing processes.
equipment age and size of plants, water
use. wastewater constituents, or other
factors required separate effluent
limitations and standards for different
industry subcategones. This study
involved a detailed analysis of
wastewater discharge and treated
effluent characteristics, including, (a)
the sources and volume of water, the
processes, and the sources of pollutants
and wastewater in the plant and (b| the
constituents of waste,waters, including
toxic pollutants. This analysis enabled
the Agency to determine the presence
and concentrations of toxic pollutants
on the major wastewater discharges.
EPA also identified several distinct
control and treatment technologies (both
m-plant and end-of-pipa), including
those with potential use in the
electroplating/metal finishing industry.
The Agency analyzed bothjiistoricai
and newly generated data on the
performance of these technologies.
including their non-water quality
environmental impacts on air quality,
solid waste generation, water scarcity,
and energy requirements.
Cost curves were used to estimate the
cost of each, control and treatment
technology. These coat curves, were
developed by applying standard
engineering, analyses to metal finishing.
wastewater characteristics. Unit process
costs were than dedved by applying
model plant characteristics, (production
and flow) to U» unit coat carve of-each
treatment process. These unit proca**
costs were added together to yield tha
total cost at each treatment level.
By considering these factor&.E?A.wa*
- able to ff^Br^ctaragg the various>control
and treatment technologies, used, a* the
baees for efSuant limitations, new
source and pretreatment standards.
However, the regulations do not require
any particular technology. Rather., they
require plants- to achieve, effluent
limitations (mg/T) which reflect the
proper operation of these technologies.
or equivalent technologies. Some
faciUties are already successfully using
technologies other- than those*relied on
by the Agency, such as dragout control,
recycle, and recovery, to achieve these
values.
rv.Data.Ca
»« Effort.
To develop the regulation. EPA began
with a review of previous work an the
electroplating/metal finishing industry.
The major source of information on this
is the Draft Development Document for
Effluent Limitations and Standards for
the Metal finishing Point Source
Category (June 1980). Several studies
completed before' this development
document was published also
contributed technical information to the
metal finishing data base for the
following segments of the industry:
• Machinery and Mechanical
Products Manufacturing.
• Electroplating.
• Electroiess Plating and Printed
Circuit Board Manufacturing (Segments
of the Electroplating Category).
• Mechanical and Electrical Products.
We also gathered data on the metal
finishing industry from literature
surveys, inquiries to professional
contacts, seminars and meetings, and
the survey and evaluation of
manufacturing facilities.
We contacted all Federal EPA regions.
several State environmental agencies.
and numerous suppliers and
manufacturers for the metal finishing
industry to collect information on: (1)
Permits and monitoring data. (2} the use
and properties of materials. (3) process
chemical constituents, (4) waste
treatment equipment (5) waste
transport. (6) and various process
modifications- to mmm™« pollutant
generation.
Under the authority- of Section 308 of
the Clean Water Act the Agency sent
three different data collection portfolios
(DCPs) to-various industries within the
Metal Brushing Point Source Category.
The first DCP obtained 4ata from 339 of
1.422 plants originally contacted from
the machinery and mechanical products
industry. The data indnded general
plant information on raw materials
consumed, specific processes used.
composition- of effluent streams, and
wastewater treatment; The second DC?
obtained date from. 38S of the 900 plants
originally contacted, in the mechanical
and electrical products industries. These
data covered, general plant
characteristics, unit operations
performed, plating-type operations.
wastewater treatment facilities, and
waste transport We sent the third DC?
to 1-883 companies involved in
electroplating. Approximately 1130
plants sent back economic analysis data
and information on general plant
characteristics, production history.
manufacturing processes, process and
waste treatment wastewater
characteristics, and treatment costs.
EPA and its contractors, also, visited
210 manufacturing facilities, to^iaiiect
• wastewater samplaund. pertinent
technical information-on-mAnufacturing
processes, and various, treatment
techniques.
V. Sampling and Analytical Program
EPA focuoad it* sampling and. analysis
on the toxic- pollutants designated in the
Clean Water Act, However, we alao
sampled and analyzed conventional and
, Prior to
undertaking, sampling-programs in
support of n'tomitking actiona. EPA had
to identify specific- toxic pollutants that
would be appropriate subjects for
investigation. The list of 65 pollutants
and classes of pollutants potentially
includes thousands of specific
compounds, the analyses of which could
overwhelm private and government
laboratory resources. To make the task
more manageable, therefore. EPA
selected 129 specific toxic pollutants for
study in this rulemaking and other
industry niicrnakings. The criteria for
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32488 Federal Register / Voi. 48. No. 137 / Friday. July IS 1983 / Rules and Regulations
choosing these pollutants inducted the
frequency of their occurrence in water.
their chemical stability and structure.
tha amount of the chemical produced.
and the availability of chemical
standards for measurement
In addition to the original 123 toxic
pollutants (of which three are now
considered nonconventional poHuiaats).
EPA checked for the presence.
frequency, and concentration of xyleoas.
alkyi epoxides. gold, fluoride.
phosphorus, oil and grease. TSS. pH.
aluminum* barium/ indium, magnesium*
molybdenum, osmium, palladium.
platinum, rhodium, ruthenium, sodium.
tin. titanium, vanadium, yttrium, *^
total phenols.
The criteria used to select plants for
sampling visits we«-..(1.) A large
percentage of the plant13 effluent
discharge should result from the
manufacturing processes listed in
Appendix C, (2) the physical layout of
plant plumbing should facilitate
sampling of the wastewater type under
study; (3) 'the plant must have waste
treatment in place; (4) the mix of plants
visited should contain discharges to
both surface waters and pubiicaly .
owned treatment works: and (5) the
selected plants should provide a
representative geographical distribution
to avoid a data bate that concentrates
on a unique geographical condition.. HP A
sampled 210 faculties' to identify
pollutants in plant wastewatera, B*tore .
visinng a plant. EPA reviewed all
available data on manufacturing
processes and. waste treatment We •
selected representative, points at which
to sample the raw wastewater entering
the treatment systems and the final
treated- effluents. Finally, we prepared.
reviewed, and approved a detailed '
sampling plan showing the selected
sample points and the overall sampfeag
procedure.
Based on this sampling plan, we then
took samples at each sample point for l.
2 or 3 consecutive days. The samples
were divided, into two analytical groups.
Within each group the samplee were
subjected to various analyses,
depending on the stability of the
pollutants to be analyzed, the various
levels of analysis wera.conducted ac (1)
Local laboratories. (Z) EPA's Chicago
laboratory, (3) contracted gas
chromaiograpjiy/mass spectrometry
(GC/MS) laboratories, and'(4) tha
sampling contractor's, central laboratory.
The sampling and analysis methods are
outlined in the Development Document
The acquisition, preservation, and
analysis of the water samples followed
the relevant methods set forth- in 40 CFR
136. Although the Agency has not
promulgated analytical methods for
many organic toxic pollutants under
Section 304(h) of the Act. a number of
these methods have been proposed for
40 CFR138 (44 FR 69484. December 3.
197% 44 FR 75028, December 18.1979).
VL Industry Suhcatagorizatian
In developing this regulation, the
Agency considered whether different
'effluent limitations and standards are
appropriate for different segments of the
metal finishing industry. The Act
requires EPA- to consider a number of
factors to determine if subcategorization
is needed. These factors include raw
materials, final products, manufacturing
processes, geographical location, plant
size and age. wastewater
characteristics, non-water-quality
environmental impacts, treatment costs.
energy costs, and solid waste
generation.
The metal finishing industry
comprises 45 unit operations. These
processes generate wastawater that falls-
into five waste groups, aaoh requiring
different treatment tor reduce the
discharge of pollutants. The five groups
are metals, cyanide, hexavalent
chromium, ails, .and solvents, with.
significant toxic organic* pollutants
potentially present in the last two.
These wastes occur in a wide variety
of combinations. Throughout the
industry, however the wastestreame are
alike in one critical sense; they all
respond similarly to the treatment
system which is already most widely
used in the industry. That system was
selected as EPA's model technology. Its
major components; io. precipitation and
clarification, are used for all waste
streams. After isolated treatment ot
hexavalent chromium, cyanide, and oil
and grease, pollutants in these waste
streams an further reduced by passage
through the precipitation-clarification
system which is also used for metal-
bearing wastes.
The-Agency has determined that the
Metal Finishing-Point Source Category
need not be subcategorized for
regulation. A set of concentration based
limitations, based on the performance
capabilities of the modal technology,
can be applied to ail metal flashing
process effluents.
EPA haajiowever decided to-exempt
indirect discharging job shops and
independent printed circuit board
manufacturers from the Part 433 PSES.
This has an effect similar to placing
them in a separate sub-category. As
noted above, this is consistent with tha
1980 Settlement Agreement in which the
National Association- of Metal Finishers
promised to withdraw its legal challenge
to those Part 413 PSES if SPA did not.
for the next several years, make them
significantly mare stringent
The Agency considered, but decided
against production based standard.
With the wide range of operations.
product quality requirements, existing
process configurations, and difficulties
in measuring production, no consistent
production normalizing relationship
could be found. Concentration baaed
limits, however, can be consistently
attained throughout the industry.
VO. Available Wastewater Control and
Treatment Technology
A. Status ofla-Placa Technology
Installed control and treatment
technologies in the metal finishing
industry generally consist of some form
of alkaline precipitation and
clarification installed at "end-of-pipe" to
remove metals. When cyanide or
hexavalent chromium wastes are
present these, waste waters are
generally segregated and treated
upstream.
3. Control Treatment Options
We examined the following control
treatment options:
Option l: Precipitation and
clarification. Stream segregation for
cyanide, hexavalent chromium and
concentrated oily wastes fallowed by
cyanide destruction, chromium
reduction and emulsion breaking
skimming as necessary. Solvent waste
segregation and removal by hauling.
Option 2: Option 1 plus filtration.
Option 3: Option l plus in-piant
control for cadmium.
VUL Qeaeni Criteria for Effluent
A. 3PT Effluent Limitations
The factors considered in defining
best practicable control tachnoigy
currently available (BPT) include: (1)
The total cost of applying the technology
relative to the effluent reductions- that
result (2) the age of equipment and
fatalities involved. (3) the processes
used. (4) engineering aspects of the
control technology, (5) process changes.
(8) non-water-quality environmental
impacts (including energy requirements).
(7} and other factors, as the
Administrator considers appropriate. In
general the BPT level represents the
average of the best existing
performances of plants within the
industry of various ages, sizes.
processes, or other common
characteristics. When existing
performance is uniformly inadequate.
BPT may be transferred from a different
subcategory or category. BPT focuses on
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Federal Register / Vol. 48. No. 137 / Friday, July 15. 1983 / Rules and Regulations
32467
end-of-pipe treatment rather than
process changes or internal controls.
except when these technologies ara
common industry practice.
• The cost/benefit inquiry for BPT is a
limited balancing of costs versus
benefits, committed to EPA'3 discretion,
which does not require the Agency to
quantify benefits in monetary terras. See
s.g., American Iron and Steel Institute v.
EPA, 528 F. 2d 1027 {3rd Or. 1975). In
balancing costs against the benefits of
effluent reduction. EPA considers the
volume and-nature of existing
discharges, the volume and nature of
discharges expected after application of
BPT. the. general environmental effects
of the pollutants, and the cost and
economic impacts of the required level
of pollution control. The Act does not
require or permit consideration of water
quality problem* attributable to
particular point sources, or water
quality improvements in particular
bodies of water. Therefore. EPA has not
considered these factors. See
Weyerhaeuser Company v. Castle, 590
F. 2d 1011 (D.C. Cir.'l97a).
B. BAT Effluent Limitations
The factors considered in defining
best available technology economically
achievable (BAT] include the age of the
equipment and facilities involved, the
processes used, engineering aspects of
the control technology, process changes.
non-water-quaiity environmental
impacts (including energy requirements).
and the costs of applying suck
technology (Section 304(b)I2)(B]). The
BAT level represents the best
economically achievable performance of
plants of various ages, sizes, processes.
or other shared characteristics. As with
3PT. uniformly inadequate performance
within a category or subcategory may
require transfer of BAT from a different
subcategory or category. Unlike BPT,
however. BAT may include process
changes or internal controls, even when
these technologies are not common
industry practice.
The statutory assessment of BAT
"considers" costs, but does not require a
balancing of costs against effluent
reduction benefits (see Weyerhaeiaery.
Castle, supra}. In developing BAT.
however. EPA has given substantial
weight to the reasonableness of costs.
The Agency has considered the volume
and nature of discharges, the volume
and nature of discharges expected after
application of BAT. the-general
environmental effects of the pollutants.
and the costs and economic impacts of
the required pollution control levels.
' Despite this expanded consideration
of costs, the primary factor for
determining BAT is the effluent
reduction capability of the control
technology. The Clean Water Act of
1977, establishes the achievement of
BAT as the principal national means of
controlling toxic water pollution from
direct discharging plants.
C. BCT Effluent Limitations
The 1977 amendments added Section
301(b)(2)(E] to the Act establishing
"best conventional pollutant control
technology" fBCTffor discharges of.
conventional pollutants from existing
industrial point sources. Section
304(B)(4) specified the following as
conventional pollutants: BOD,TSS. fecal
coliform. and pH. The Administrator
designated oiLand grease-as
"conventional" on July 30.1979. 44 FR
44501.
3CT is not an additional limitation but
replaces BAT for the control of
conventional pollutants. In addition to
other factors, specified in section
304(bj(4)(B). the ACT require*-that BCT
limitations be a**e**ed ia light of. a (wo
part "cost-ceeaonablenee*" test
American Paper Institute v. SPA, 680 F.
2d 954 (4th Or. 1381); The first test
compares the cost for private, industry to-
reduce its conventional pollutants wiin
the costs to-publicly owned.treatment
works for similar levels of reduction in
their discharge of.theae pollutants. The
second test examine*, the coat-
affectivermss of additional industrial
treatment beyond BPT. EPA must find
that limitation* are "reasonable" under
both tests before-establishing them as
BCT. In no cage may BCT b« less
stringent than BPT.
EPA published its methodology for
carrying out the BCT analysis on August
29.1979. (44 FR 50732). In the. case
mentioned above, the Court of Appeal*
ordered EPA to correct data error*
underlying EPA's. calculation of the first
test and to. apply the second coat test
(EPA had argued that a second coat test
was not required).
BCT limitations for this industry were
proposed on October 29.1982 (47 FR
49176). They were accompanied by a
proposed methodology for the general
development of BCT limitations. BCT
limits for this industry will be
promulgated with, or soon after, the
promulgation of the final methodology
for BCT development At that-time EPA
will respond to relevant comments filed
in either that ruiemalting or in this one.
D. New Source Performance Standards
The basis for new source performance
standards (NSPS) under Section 306 of
the Act is the-hest available
demonstrated technology. New plants
have the opportunity to design the best
and most efficient metal finishing
processes and wastewater treatment
technologies. Therefore. Congress
directed EPA to consider the best
demonstrated process changes, m-plam
controls, and end-of-pipe treatment
technologies that reduce pollution to the
maximum extent feasible.
£ Pretreaanent'Sfandards for Existing
Sources
Section 307(b j of the Act requires EPA
to promulgate pretreatment standards
. for existing sources (PSES), which
industry must achieve within three years
of promulgation. PSES are designed to
prevent the discharge of. pollutants
which pass through, interfere with, or
are otherwise incompatible-with the
operation of POTW s.
The legislative history of the 197? Act
indicates that pretreatment standards
are to be technology-based, analogous
to the best available technology for
removal of toxic pollutants. The General
Pretreatment Regulations which serve-as
the framework for the final metal
fir^«hmg pretreatment standards are in
40 CFR Part 403. 49 FR 9404 Qanuary 23.
1981).
EPA ha* generally determined that
there is pas* through of pollutants if the
percent of pollutants removed by a well-
operated POTW achieving secondary
treatment is las* than the percent
removal by the BAT model treatment
system. A study of 40 well-operated
POTW 3 with biological treatment and
meeting secondary treatment criteria
showed that regulated metals are
typically removed at rates varying from
20 to 70%. POTWs with only primary
. treatment have even lower rates of
removal In contrast, SAT level
treatment by metal finishing industrial
facilities can-achieve removals of
approximately 97% or more. Thus it is
evident that metals from this industry do
pass through POTWs. As for toxic
organic! data from the same POTWs
illustrate a wide range of removal, from
0 to greater than 99%. Overall POTWs
have removal rates of toxic organics
which are lea* effective than the metal
finishing TTO technology basis of no
dumping of toxic organic wastes. The
POTWs effluent discharge of specific .
toxic pollutants ranged from 0 to 4.3
milligrams/liter. Many of the pollutants
present in metal finishing wastes, at
sufficiently high concentrations, can
inhibit biodegradation in POTW
operations. In addition, a high
concentration of toxic pollutants in the
sludge: can limit POTW use of sludge
management alternatives, including the
beneficial-use of sludges on agricultural
iands.
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32468 Federal Register / Vol. 48. No. 137 / Friday. July 15. 1983 / Rules and Regulations
Section 307 oi the Clean Water Act
provides that POTWs may grant credit
to indirect dischargers, based on the
degree of removal actually achieved at
the POTW. EPA has General.
Pretreatment Regulations regulating
POTWs' authority to grant such credits.
A Federal Register notice of
September 2& 1982 explained EPA's
latest data and proposed national
removal credits for well operated
POTW's achieving the national
secondary treatment limits. See 47 FR
42898. That proposal is not being relied
on in this ruiemaking: however if such
credits are available the costs of today's
standards could be sustantially reduced,
F. Pretreataient Standards for f/ew
Sources
Section 307fcj of the Act requires EPA
to promulgate pratreatment standards
for new sources (PSNS) at the same time
that it promulgates NSPS. These
standards are intended to prevent the
discharge of pollutants which pasa
through, interfere with, or an otherwise
incompatible with a POTW. New
indirect dischargers, like new direct
dischargers, have the opportunity to
incorporate the best available
demonstrated technologies—including
process changes, in-plant controls, and
end-of-pipe treatment technologies—and
to select plant sites that ensure the
treatment system can be.adequateiy
installed. Therefore.'the Agency sets
PSNS after considering the same criteria
considered for NSPS. PSNS will have
affluent reduction benefits similar to
NSPS.
DC, Summary of Final Regulations
In the electroplating/metal finishing
industry, the pollutants of concern are
cadmium, chromium; copper, lead.
nickel, silver, zinc, cyanide, toxic
organics. TSS. oil and grease, and pH.
The treatment option selected for each
effluent limitation, pretreatment
standard and new source performance
standard is based on the criteria
specified in the Clean Water Act The
technologies are discussed in more
detail in the Development Document for
this ruiemaking.
A. Part 433
The pollutants being regulated under
3PT limitations are cadmium, copper.
chromium, nickel, lead, silver, zinc, total
cyanide. TSS. oil and grease and pH.
Total toxic organics (TTO) is also being
regulated. Compliance with the TTO.
limit basically involves not dumping
concentrated toxic organic wastes, e.g..
solvent degreasers and paint stoppers.
Other sources are generally small.
infrequent and of low concentrations.
For SPT. EPA is setting limits
achievable by technology- based on
precipitation and clarification far all
metal finishing effluents. In addition, for
cyanide or hexavaient chromium the
technology basis incorporates
techniques to destroy cyanide and
reduce hexavaient chromium to its
trivalent state. These effluent limitations
reflect the average of the best existing
control technologies widely used, in the
industry and remove approximately 97.9
percent of the raw waste of toxic metals
'and cyanide, and 99 percent of the toxic
orgamcs discharged. The technology is
consistent with that used as a basis for
PSE5 for the electroplating industry
(January 28.1981.40 FR 9462) and the
March 28.1974. suspended. BPT
limitations. The limitations are derived
in the manner discussed in the following
section. They are generally more
stringent than those found in currently
effective electroplating, pretrsatment
regulations, because EPA is now- using a
revised and updated data base.
For SAT. EPA is establishing
limitations for the toxic pollutants and.
at a level equivalent to BPT. The Agency
seriously considered setting SAT and
SAT-level PSES limitations based on
BPT level technology plus filtration.
Filtration would have led to an
additional capital cost of almost S1.2
billion. In light of the statutory mandate
to consider cost in setting BAT, EPA
decided to refect the filtration option.
because of its very high aggregate cost
on a nationwide basis. We did not select
ini-plant cadmium control because it can
require significant re-engineering of
process water flow and of product and.
equipment handling, on a plant-by-plant
basis. The changes vary widely and in
many cases could be difficult for
existing plants to apply. The compliance
date for BAT is no later than July 1.
1984. the maximum time allowed by the
Act
For NSPS. EPA is establishing .
limitations based on BPT/BAT
technology plus in-plant control of
cadmium. This additional control takes
advantage of a new plant's ability to
achieve effluent reductions of 89%
beyond BAT cadmium levels. The
pollutants regulated under NSPS are the
same as those regulated under BPT
limitations.
For PSES in the Metal Finishing
Category, limitations are based on
technology equivalent to BAT and BPT.
The pollutants regulated under this
PSES are the same as the toxic
pollutants regulated under BPT (BAT]
limitations. A study of 40 well-operated
POTWs with biological treatment and
meeting secondary treatment criteria
showed that regulated metals and
cyanide are typically removed at rates
varying from 20 to "0%. POTWs with
primary treatment have even lower
rates of removal. In contrast, metal.
finishing PSES-ievei treatment can
achieve removals of approximately 97".
Thus it is avident that metals and
cyanide from this industry do pass
through POTWs. As for toxic organics.
data from the same- POTWs illustrates a
wide range of removal, from 0% to
greater than 99%. Overall POTWs have
removal rates of toxic organics which
are less effective than the metal
finishing TTO technology basis of no
dumping of toxic organic wastes. The
POTWs effluent discharge of specific
toxic pollutants ranged from 0 to 4.3 ms/
1. Many of the pollutants present in
metal finishing wastes at sufficiently
high concentrations can inhibit
biodegradation in POTW operations. In
addition, a high concentration of toxic
pollutants in the sludge can limit POTW
use of-sludg* management alternatives.
including the beneficial use of sludges
on agricultural lands.
The compliance date for the metal
finishing PSES is
February 15.1986 for metals, cyanide.
and TTO. Agency analysis indicates
that facilities can plan, design, and
install the necessary equipment in 31
months, which will be allowed by the
specified compliance date. There is also
a June 30.1984 compliance date for an
interim toxic organic limit, which can be
met by in-house management and
handling controls.
For PSNS. limitations are based on
technology equivalent to NSPS. The
pollutants regulated under PSNS are the
same as the toxics regulated under
NSPS. As with PSES. these pollutants
are necessary for control in PSNS to
prevent pass through, interference, and
sludge contamination.
&, Part 413.
Indirect discharging-job shops and
independent printed circuit board
manufacturers will continue to be
regulated under the existing PSES for
Electroplating. This is consistent with a
1980 Settlement Agreement in which the
National Association of Metal Finishers-
and the Institute for Interconnecting and
Packaging Electronic Circuits agreed not
to challenge, the Part 413 pretreatment
standards for existing source
eiectroplaters. in return for the 1981
amendments and. an EPA commitment
that in light of their economic
vulnerability, EPA did not plan to
develop significantly more stringent
standards for those plants for the next
several years.
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Federal Register / Vol. 48, No. 137 / Friday, July 15. 1983 / Rules and Regulations 32469
Control of toxic organics is being
added to the requirements far facilities
- under the Electroplating PSES.
Examination of the technology
requirements, costs, economic impact
and timing indicates that requiring
control of toxic organics is consistent
with the Settlement Agreement
First it will not increase the economic
vulnerability of job shops or
independent printed circuit board
manufacturers. Compliance with the
toxic organic standards can be achieved
by good management practices (i.e., not
dumping waste solvents into the
wastewaters). No additional end-of-pipe
technology (beyond that already
required by Part 413) is necessary.
Economic analyses reveal that control of
toxic organics does not impose
significant additional costs or impacts.
Second, these facilities are being
allowed 3 years to comply with the toxic
organic standard. Thus, even if control
of T7Q were considered "more
stringent", the time allowed for
compliance will amount to a years from
the date of the Settlement Agreement
That fulfills the Agency's obligation not
to develop more stringent standards for
these facilities in the next several years.
X. Derivation of the Limitation*
EPA began development of these
standards by building on the
information obtained in developing the
Electroplating Pretreatment Standards.
For Metal Finishing. 2783 companies
were contacted aa part of two surveys
(one of .1190 plants and the other of 365
plants) and 1555 useable questionaire
responses were obtained. The Agency
also selected 322 plants for visits and/or
obtained long term self-monitoring data
on them.
The data gathering effort was the
basis for the Agency's first two critical
determinations. First pursuant to
Section 307(b) of the Act EPA identified
those pollutants that would pass through
or interfere with a POTW, or its sludge.
Second. EPA discovered that a basic
and "classic" pollution control
technology was widely practiced in the
industry. The system is designed to
remove toxic metals from raw
wastestreams and if has two principal
components—precipitation and -
clarification. Of 1190 surveyed plants.
689 reported treatment present, of these.
428 facilities practiced the precipitation
of metals through pH adjustment of
wastewater.
EPA then analyzed the data to
discover what those classic-and
commonly used treatment devices could
achieve. For each regulated pollutant
EPA looked for two key figures: The
average concentration that properly
operated technology would achieve over
time, and the variability from that
average that would be inevitable even
at well-operated plants.
To find long-term concentration
averages. EPA examined its file of 322
pjants which had been visited and/or
had sent long-term self-monitoring data
to EPA. Of these plants EPA had
sampled 72 with precipitation and
clarification. After deletions for
improper treatment dilution, andiow
raw waste concentrations, 30 plants
(sampled by EPA from 1 to 8 days) wen.
used for developing the long-term
concentration averages. For these
plants. EPA had obtained detailed
information on treated and untreated
(raw) wastewater characteristics.
For most pollutants the average of this
data was used for the long-term average.
EPA sampled data for cadmium and
lead appeared too low to represent the
range-of raw wastes in the industry. For
these, parameters EPA used available
self-monitoring data to calculate the
long-term average. Although the Agency -
has less information on which to judge
the adequacy of treatment is the self-
monitoring data, these higher values
wen used by the Agency to compensate
forthe relatively low raw waste
cadmium and lead at EPA sampled
plants. The avenge, of the self-
monitoring data for lead and cadmium
was used for the long-tenn average.
The regulations specify dairy and
monthly average maximum*. Thus, the
limits are developed from- the Agency
assessment of long term concentration
averages multiplied by variability
factors. If a plant intends to consistently
comply with the regulatory limit it
should use the long term concentration
average as the basis for design and •
operation. The following long-term
concentration avenges wen found to be
attainable by the technology EPA
assessed, and wen costed in this -
rulemaking. They are presented here as
guidance to dischargers and control
authorities:
Lang Tarn Concentration Average*
lmq/11
040mm, (Tl
ChramwmfT)
Caw (T)
0.13
0.57S
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32470 Federal Ragiatar / Vol. 48. No. 137 / Friday, July 15. 1983 / Rules, and Reguiatioaa
from 0.17*lo O20 mg/1,anc changed
from 0.582 to 0.549 mg/1. and cadmium
changed from 0.19 to ai3- mg/t
The derivation of the proposed TTO
limit did not distinguish differences
between plants. Comments-suggested
that plants with certain processes
should b* allowed a higher limit EPA in
response, examined grouping of plants
by sources of TTO: e.g, these that
perform solvent degreasing. and/or
painting, plants which- performed both.
solvent degreasing and painting'had
higher raw -waste TTD than any other-
process group. The final TTO Hnritis-
based on that process gtuupiug. which is
a conservative assumption since H had
Furthermore. EPA is now promulgating
two ITtj limits for plaints i.uveteil by
Part 433. Tire first is based soieiy on
background levels found prior to end-of-
pipe- tmttiBent. It most be met by JmiQ-
30.1384. accept that plants covered by
Part 430 (arm and ategij need not meet It
mrtfl fui? 10.1383. The-seedhdiTTO limit
is baaed 90 effluent data andtakes into
3ccotmt t&o AOCUuOfiu rviXLWBfl
acutfivoa by 9nd*ot*pTp* tmtmnt. 'Hits
36GODGL uxrat iznst TW met by Frornary
IS, 198ft Most facilities should be able
to meet this limit after installing «nd-crf-
pipe tteauneatto meet the electroplating
PSES of Pait«3. However Part 433
allows the period until February 15.1368.
in caavaddrticmsi process stream* -
present -special cotnpSaitce problems.
For PSES. job shops and independent.
printed circuit board manufacturers are-
regulated only -under Part «3. They will
have until July 141988 to comprjr-witt*
,. TTO. Thus "seveai years'* will nave
fboowad the SettJemaw Agreement of
1980,
In .calculating variability factors.
dmtgjw -were mode to bom- the daily
*M^^^iiiTp *MMflajy^|y 30j thirty day*
vaoabiliiy. First the daily maximum
variability wea-calcaiatecHn the
proposai by using Jogtffirmal ataastica
lor pfaat* with lew than 100 jaapfcaf
days-aod a nonparamatnc procedure-far
plants reporting 100 or more
observations. For the final regoctaoa 4se
Agency found that the larger data sots '
had a good fit to the lognormai
distribution. Thus the Agency ia-unai
the lognormai procedure for all data
sets. -Second. 30 day limits baaed oo tn» •
average of 30 samples have bean-
replaced with a monthly avenge baaed
on 10 samples per reporting period. This
is consistent with other recent Effluent
Guidelines for similar industrial
categories.
In addition, the Agency responded to
comments that tba,statistical
methodology used in proposal did not
predict percent exceedancaa of,th« 30
day limits consistently with the 98%
criterion used to derive the limits. The-
mam. reason for thia waa that day to day
dependence in the data was nut
accounted for in dornrinj the proposed
limits. In deriving the 10 sampl* monthly
iimita. the Agency examined data
dependence -ia tares ways. First, by
fitting diet data to a ataouicai time-
series nrvjflii n**uMii't1 gy incorporating,
direct computations of auto-carmacions
into derivations of tha linritx and tfard.
by Sittog oburved jaqnaBcaa of 10 day
average* to a lognomiai distribiirinn.
The fiuai monthly limits were
determuiaal by fittotg observed
sequence* of 10 day averages to a
lognonnal disaiboaoa beeaoae this
provideii the aaet aaafantoiy at to the
data. The ytivwk e£foct of these
statistical changes, ws ta aa» aoma
limits.
Another change ia that aa alternative
^rfffltiHkkf ffya^y^ limiti* "^^^^
avaUabte to ^alirjeswim agnSflcant
form*
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Federal Register / Vol. 48. No. 137 / Friday, July 15. 1983 / Rules and Regulations 32471
municipalities and permit writers to
monitor 10 days per month, the total
annual costs increase by SSI million
from S118 million to $179 million. No
'closures or employments effects are
projected to result from this level of
monitoring; the average increase in cost
of production would be 0.03 percent
versus the 0.02 percent presented above.
The Agency has determined that this
regulation would be economically
achievable even if all facilities are
required to monitor 10 days a month. No
measureable balance of Bade effect is
expected from this regulation due to the
estimated small change in the pnce of
metal'finishing products.
3PT
Direct discharging facilities are not
expected to incur costs to comply with
the metals and cyanide limitations
because these facilities are already
covered by NPDES permits which set
BPT limits on case-by-case best
engineering judgments. A1981 survey of
randomly selected permits indicates that
nearly all existing permits specify limits
equivalent to, or more stringent than.
those contained in-this regulation.
Direct discharging facilities may incur
costs to comply with the limitation on
total toxic organics. EPA assessed, TTO
compliance costs on the assumption that
ail plants would incur baseline "
monitoring costs of $1.304 an a one time
basis. EPA believes that almost all
plants will then comply through the
certification process. Nevertheless, EPA
assumed that those facilities which
currently dump would not be able to use
the certification process and would
incur annual compliance costs. (This
same procedure was used for TTO
compliance under PSES.j EPA has
assumed that the annual BPT
compliance costs could be $29.000 for
job shops, $34.700 for independent
printed circuit board manufacturers and
3488.000 for captive shop facilities.
These costs apply to 10 out of 388 direct
discharging job shops, 12 out of 44 direct
discharging independent printed circuit
board manufacturers, and 182 out of
2.500 direct discharging captive shop
facilities. Increases in the cost of
production resulting from the control of
TTO are not expected to exceed 0.9
percent. No closure or employment
effects are projected for these sectors.
air
Since the BAT limitations are the
same as the BPT limitations, there is no
incremental cost or impact associated '
with compliance with the BAT
limitation:.
PSES
Indirect discharging job shop and
independent printed circuit board
facilities are expected to incur costs
only to comply with the TTO limitation
which is-being added to the
electroplating pretreatment standards in
Part 413. This TTO limitation is included
in the regulation because compliance
will significantly reduce toxic organic
pollution and will cause negligible
economic impacts on these industry
sectors. EPA is not imposing metals and
cyanide limitations more stringent than
those specified in the existing applicable
pretreataent standards despite
evidence that such limits can be reliably
achieved by the technology that forms
the basis of the current standards. This
is consistent with a March 1980
Settlement Agreement in which the
relevant trade-associations agreed-not to
challenge the Part 413 pretreatment
standards for existing source
eleclropiaterSe
Approximately 77 of an estimated
2.734 indirect discharging job shops and
38 of the 327 indirect independent
printed circuit board manufacturers are
assumed to incur'costs to comply with
the TTO standard. Annual costs of
$222,500 and $254.300 respectively are
projected for the two sectors. The
average annual cost per facility to
comply with the TTO limitations is
approximately $2900, primarily for
sampling and analysis. No closures or
employment, effects are projected for
these sectors. Production cost increases
an expected not to exceed 0.03 percent
for the two sectors.
Non-integrated indirect discharging
captive facilities-with effluent flows
greater then 10,000 gallons per day an
assumed to incur additional costs to
comply with the TTO standard. Control
of metals and cyanide can be achieved
through capital investment already
required by currently effective
electroplating regulations. Although the
metals and cyanide standards
promulgated today are more stringent
than those in the currently effective
electroplating regulations, they can be
met through use of the same pollution
control equipment relied on to meet the
electroplating pretreatment standards.
The $167.500 of annual costs associated
with control of TTO applies to 58 of the
900 nonintegrated captive indirect
dischargers with flow-greater than
10,000 gpd. No closure or divestitures
are expected to occur.
Non-integrated indirect discharging
captive facilities with flows less than
10.000 gallons per day will incur costs
from both the metals and cyanide
standards and the TTO standards.
Unlike the prior-group with Hows greater
than 10.000 gpd, this group was
generally exempt from Part 413's
precipitation/ clarification based
pretreatment standards. Their inclusion
in-the metal finishing standard could
necessitate investments in both end-of-
pipe and in-plant treatment
technologies. The cost for these facilities
to comply with the metals and cyanide
* standards totals $11.8 million annually.
These costs apply to 912 out of an
estimated 2850 nonintegrated indirect
discharging captive facilities with flows
less than 10.000 gpd. Data indicate that
the remainder of these plants already
have adequate treatment in place. The
annual cost to comply with the TTO
standard is $534.600; this applies to 135
facilities. The average increase in the
cost of production is approximately one
percent No closure or employment
impacts an projected.
Of the.3.750 facilities in the last
industry sector, integrated indirect
discharging captives. 1.200 may incur
aggregate costs of $104 million annually
to comply-with the metals and cyanide
standards and 243 of these facilities may
incur costs of approximately.$705,000
annually to comply with the TTO
standard. Integrated shops perform
metal finishing operations in addition to
electroplating processes. Thus, they are
affected by the existing electroplating
standards as well as by today's
regulation. EPA anticipates that the
integrated facilities will comply with the
metal finishing standards by treating
their total process discharge through a
jingle treatment system that would be
more costly, than the one required solely
to treat electroplating waste-waters.
The costs indicated above reflect the
additional costs of complying with the
metal finishing standard: the
electroplating costs were reviewed in an
earlier regulation 40 CFR Part 413. 44 FR
52590, September 7.1979 and they serve
aa the baseline for determining the
impacts of the metal finishing regulation.
To determine the baseline costs required
to comply with the electroplating
pretreatment standards, EPA first
revised its earlier estimates, based on
updated surveys of treatment in place.
improved estimates of the population of
affected captive shops, and calculated
costs attributed to the electroplating
flow of integrated captive indirect
dischargers. The revised estimate (in
1982 dollars) indicates that this sector's
costs for compliance with the
electroplating pretreatment standards
are $512 million in capital costs and $169
million in annual costs, including
interest and depreciation. EPA now
estimates that the major economic
392
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32472
Federal Register / Vol. 48. No. 13? / Friday, July IS, 1983 / Rules and Regulations'
effects of that regulation would be 24
plant closures and six electroplating
divestitures which could result in 896
job losses and 34 job transfers.
In estimating the economic impact ox
today's metal finishing regulation. EPA
assessed the costs of treating the
additional Sows covered by today's
regulation at the model plants used in
the electroplating analysis. The costs .
used in conducting the economic impact
analysis reflect the cost of treating ail-
process flows, expect for the six
electroplating process streams- specified
in Part 413. To the extent these flows
include processes oat regulated under
metal sighing, tiie costs and resulting
impacts overstate the effect of thametai
finishing regulation.
SPA's estimates of the effects of these
regulations ace based on a sample of
approximately 1.100 plants. The results
heve been extrapolated to the Cull
population of &750 plants in this- sector.
For each model plant the analysis
determines the- incremental incr&ase in
the-costs of production to comply with
the metal fin
plant's compfiancs casts relative- to
sales are high, the analysis projects
metal finishing process One divestitures
or plant closures. Additional impacts.
thus, are those due to today's metal
finishing ragiilajinn nniy. IgyegQQeBi
costs are expected to total
approximately 33S1 million, while
annual costs are projected to be
approximately S118 million, '"^"fting
interest and depreciation. The annual
costs represent approximately n ??
percent of the 280 billion «"»"«! valoe of
shipments from integrated 'T*^*yrt
captive plants. EPA's analysis protects.
that this would lead to oe plant closures
or process line divestitures, and that no-
employment disruption would result
The TTO portion of these total a"m"'1
costs shown above is approximately
5705.000. TTO costs apply to 243 of the
3750 integrated indirect discharging
capove- facilities.
Finally, EPA assessed the combined
impact of today's regulation -and the
electroplating pretreatment regmatioa
on the captive integrated indirect
discharging sector of me industry* Tliis
analysis, like those for eledropiating
and metal {hushing alone, was based on
costs for the treatment technology used
for the development of the limitalfrms.
Some- plants may receive removal
credits or install less expensive
technology. In addition. EPA has
deferred the compliance, date lor
integrated facilities, thereby allowing
plants additional time to plan for
compliance and not be subject to
treaonent.costs. This analysis avi^t^t
that the combined investment for the
captive integrated indirect discharging
sector for bom regulations was 3827
million, with animal costs of S274
million, including, interest and
depredation. Thirty plants (out of 3J50)
might divest their electroplating lines or
dose, and 980 jobs (out of 450.000) could
be lost or displaced. These impacts are
the seme as those due to the
electroplating preoeatment standards
alone. No additional closures,
divestiture's, or* uitemploymB&t effects.
are expected from the more stringent
standards promulgated today.
ffSPSandPSNS
Finally, the noairementa for new
sources are the same-as those for
existing sotsrssa* except that cadmium
must be controlled more stringently. The
incremental cost of compliance wrth the
cadmroa-contrBi ranges from 314.000 to
$24.000 par facility depending on the
water flow. Tisse costs represent
between CUE and 2.0 percent of
• projected vataairf sales for these
facUitiesk Since cadmntm plating occurs
at only abort 153S-of tha facilities and in-
plant consols frlt" be designed into new
facilities, there is expected, to be no
competttr™ disadvantage for new
sources iniiHnn to enter the industry.
Total Toxic Organic!
EPA's ""••""•"' analysis of tfae-TTQ
limit had its own costing memodoigy. Its
results were incorporated into the
impact analyses for the other specified
limits. £PA .believes, however, mat a
ceroficatioa procedure will make these.
costs unnecessary in almost all cases. •
Tie, Agency- is offering the
certificaaoa- procedure as as alternative
to self-monitoring because frequent.
monitoring Jar toxic orgaaics could be
expensive. Under* the certification
procedures facilities •**"* identify ****
toxic organics jjsed and certify mat the
resultant wastes are being properly
hauled. The Agency axpecti that almost
all plants mflcartify.
Some plants aay still be required to
monitor. However, estimating the.
number of £aeilltias mat may still be
requind to monitor TTO must be
anrrsnrilisiied indirectly, because dun
is oo history to indicate how cootroi
authooties will apply toxic organic
requiremeDB) JM*J certification
alternatives to .monitoring. The Agency
exsmuwd rwo indicators of the need to
require monitoring. Tha first was tha
percentage of plants that currently dump
waste solvent degreaaen. This
percentage may approximate the
population .size that control authorities
need to-chadc. Only 24* of the captives
use solvent degreasing. which is the
primary source of potential toxic organic
violations in these wastewaters.
-Comparable figures are 10.3% for ]ob
shops and 100% for printed circuit board
manufacturers.
Thes* wastes can profitably be
recovered by the plant and some waste
haulers, who pay for waste solvents.
have been identified, and are cited in
the public record. Approximately 73% of
the facilities which ""»•"» solvent
degreasers. already properly dispose of
this -waste. However even the 27% of the
population who now dump their
solvents will probably stop that practice
and be eligible for certification. In
addition some of the solvent degreasers
that these plants use do not contain any
toxic organic*. Other sources of toxic
orgaaics present at metal .finishing
plants may compensate for the Agency's
conservative assessment on decreasing
but this should not be significant since
dumped solvent degreasers are clearly
the single most' significant source of
TTO ia wastewaters. Thus this
approach leads to a conservative
overestunatioa by the Agency.
The second approach was to examine
the percentage of ERA sampled data
which exceeded the TTO limit and to
consider this as a measure of the
fraction of facilities needing monitoring.
This was 2J percent of the data (i-a.
97.4* of sampled data already complies
with the TTO limit). The 2.3 percent
exceedance rale of the TTO limit during.
EPA's «jn»p«ng supports the need for
certification and for control authorities
to establish reasoned plant specific
monitoring frfianeacias.
For purposes of fmnnnm; analyses
the number of facilities coated for TTO
monitoring wes estimated to be
equivalent to-the number of facilities
currently dumping solvents. The
economic impact analysis also
performed two sensitivity analyses. The
first was wits a greater number of plants
monitoring for TTO. The second
a*mmrm**i that pleats monitored for TTO
monthly instead of quarterly. Both
changes led ttkoniy slightly different'
impacts. AU.scenarios--were.found to-be
acceptable and economically
achievable.
Sunwtufy
The Agency concludes that the final
regulation is economically achievable.
and the impacts are justified uTlight of
the affluent nriwrtt'™ achieved. The
metal fi««^"^ regulation will remove
an additional 20 million pounds per year
of metals and cyanide and 10 million
pounds per year of toxic organic*,
393
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Federal Register / Vol. 48, No. 137 / Friday, JuJy IS. 1983 / Rules and Regulations
32473
3. Executive Order 12291
Under Executive Order 12291 the
Agency must determine whether a
regulation is "Major" and therefore
subject to the requirements of a
Regulatory Impact Analysis. Major rules
impose an annual cost to the economy
of S100 million or more or meet other
economic impact criteria. Based on the
Agency's estimates this regulation could
have an annual effect on the economy of
more than 5100 million, making it a
major regulation.
Executive. Order 12291. does not
require-a Regulatory Impact Analysis
where its consideration would conflict
with the development of-regulations.
pursuant to a court order, as with tins.
metal finishing regulation. EPA. has
prepared, however, an-analysis that
contains, many of the element* of. a
Regulatory Impact Analysis-, A-cop? of
the analysis cao.be obtained.fram.Aiec
Mcflnde, Monitoring and-Data,Suppon
Division. WH-553, US. EPA, 401M.
Street S.W., Washington, D.C 20480..
C. Regulator? Flexibility Analysis
Pub. L 99-354 requires that a
Regulatory Flexibility Analysis' be
prepared for. regulations, that have a
significant impact on a. substantial
number of small entities. The analysis,
may be done in conjunction with, or. as-
part of. any other analysis conducted by
the Agency.
A small busine9*.anaiy*tt is.uiciuded.
in the economsc.impact,analy«»s,Tai»,
analysis shows that there wiQ not ha-a.
significant impact on any segment of the
industry, large or small. Therefore, a
formal Regulatory Flexibility Analysis
was not required.
D. SBA Loaar
The agency is continuing to. encourage
small plants—including circuit board
manufacturers—-to use-Small Business.
Administration (SBA] financing as
needed for pollution control equipment.
The three basic programs are: (1) TSe
Guaranteed Potation Control Bond
Program. (2) the Section 503 Program.
and (3) the Regular Guarantee Program.
All the SBA loan programs are- only
open to businesses that have: {a) net
assets less than 56 million, and (fa) an
average annual after-tax income of less
than S2 million, and (c) fewerthan 2SO
employees.
For further information and specifics
on the Guaranteed Pollution Control
Bond Program contact: U.S. Small
Business Administration. Office of
Pollution Control Financing. 4040 North
Fairfax Drive. Rossiyn, Virginia 22205
(703) 235-2902,
The Section 303 Program, as amended
in [uly 1980. allows long-term loans to
small and-medium sized businesses.
These loans are made by SBA approved
local development companies. These
companies are authorized to issue
Government-backed debentures that are
brought by the Federal Financing Bank.
an arm of the U.S. Treasury.
Through SBA's Regular Guarantee
Program, loans are made available by
commercial banks and.are guaranteed
by the SBA. Tiia-program has. interest
rates equivalent to markat.rates.
For additional inforn»tioB.on.the
Regular Guacante»aad.Sectioni503.
ProgramfrcaatactyaaE district or local'
SBA- Offiea, Thsseoordiiutor ae EPA
headquartarsi.is-.Ms. FrancatQeaeette
who may>be:reacind-at.(2a2T38Zr-33Z&
XrV..Non-Water-<2uality Environmental
The eirn
form of pollutunranp
environmental-problems- Sections'
and 30&of the Actrequirt EPA to
consider the- non-wwer-onaiity
other
requirements) of. aertaa- regulations. To-
comply, EPA eoimdei etfctfaeegeet -of
this,regnlatje»os-air: noraevpadrenon.
and aoiiriv waste-ijeiiBi aiiuiu aggie.
balantinffpotiatioirptoblems\ags0ist
each otinraaevafouiat energy use-is
difficult EPA bOHVf^That'ias'fmai
regulaaon.hujjt1 JBI imii-gvergU:narlonai
goals*
Thrfc^owinsrarertnenon-water*
quality envnrsnnental impacts
(including energy reqrnrenientsl
associated with, today's regniaJlotr.
A. Air Poilotaa
Compliance, with the.BPC.aKT, NSPS,
PSES, and PENS will not.create any-
substantial air pollution-problems.
Alkaline chlorinatSon for cyanuia.
destruction endchromiuni reduction
using sulfur dioxide may produce some
emissions to the atmosphere*
Precipitation and-danfication. the major
portion of the technology basis, should-
not result in any air pollution problems.
In addition, control of total toxic
organics at the source will result in a
decreaseurtne- volatilization of solvents
from streams and POTWs.
£. Nois*
None of the wastewater treatment
processes cause significant
objectionable noise.
C Radiation
None of the treatment processes pose
any radiation hazards.
0. Solid Waste
EPA has considered the effect these
regulations would have on the
accumulation of hazardous waste. »•
defined under Section 3001 of the
Resource Conservation and Recovery
• Act (RCRA). SPA estimates that the BPT
and BAT limitations will not contribute
to additional solid or hazardous wastes.
However. PSES will increase the solid
wastes'from these plants by
approximately 185.000 metric tons per
year. This sludge'can be hazardous
because it will necessarily contain.
additional'quantities (and
concentrations) of toxic-metal
pollutants. Disposal of these wastes was
coated as though they were hazardous.
EPft'3 Office ofSoadrWaste has -
anaiyzed-tbe saiid*waste-management
and disposal costs* required' by the
industry!} compliance- with RCHA
requirements. Some-results-were*
.pubnshettin-45711 33986 (May 19,1980f.
In addition. RGMjcostB'havebeen
included in.tnwcostt.-antr economic
impact anaiyswdtmng^'tJie development
of this regoiation. However, since
November 1990. EPA- na* received: 196
petitions to-deiis* wastes, from' metal
finishing>faciUtiea.-S«venty-«euen.ha-ve
been granted. 104.are-pending, and 15
have been-rejected.. Thus it-appears- that
the.deosion.to cost jll.-sol '
overstated. likely. co«ts^ Furthermore-, the
Agency has.not assessed the savings
Hkeiy to occur because of reduced
contamination. of.POXW sludges. Those
savings-are likely to becanajderabie,
EPA estiaiatefcthat achioving; the BPT
and BAT effluent limitations will not
increase electrical energy consumption.
The Agency estimates that PSES will
increase eieetncar-gnergy consumption
by approximater? 142 million kilowatt-
hours per year. For a typical existing
indirect discharger, tins-will increase
energy con»umpaon less- than one
percent of the total energy consumed for
production*
The- energy requirements for NSPS
and PSNSarfceXnnated.to.besirnslar to
energy reqriiien»nr.forBAT. However.
this can.oiriy be quantified in inwh/year
after pro-ecttons.are-made fornew piant
construction.
XV. Best Management Practices (BMPs)
Section 304(e) oftha-aean Water Act
authorizes the Administrator to
prescribe "best management practices"
("BMPs"1. EPA.may develop BMPs that
apply to all industnai.sites or to a
designated industrial category, and -may
offer guidance to permit authorities in
394
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32474 Federal Register / Vol. 48. No. 137 / Friday. July 15. 1983 / Rules and Regulations
establishing management practices
required by unique circumstances at a
given plant
Although EPA is-not prescribing them
at this time, future BMPs could require
dikes, curbs, or other measures to
contain leaks and spills, and couid
require the treatment of toxic pollutants
in these wastes.
XVL Upot and Bypass- Pluntsiuas,
A recurring issue is whether industry
limitations and standards should include
provisions that authorize noncompliance
during "upset" or "bypasses." An upset
sometimes called an "excursion," is-
unintentional noncompliance beyond
the reasonable control of the permittee.
EPA believes that upset provision* are*
necessary, because upsets will
inevitably occur, even if the control
equipment is properly operated. Because)
technology-based limitations can require
only what technology can achieve, many
claim that liability for upsets is
improper. When confronted with thu
issue, courts have been divided on tfaa
questions of whether an explicit upset or
excursion exemption is necessary or
whether upset or excursion Incidents
may be handled througn.EPA's
enforcement discretion. Compare
Marathon Oil Co. v. EPA. 564 F. 2d 1253
(9th Clr. 1377) with WeyernaeiMarv.
Castle, supra and Cam Refiners
Association, at oJ. v. Coatit, No. 78-1009
(8th Or. April 2.1979). See also
American Petroleum Institute v. EPA.
340 F. Zd 1023 (10th Or. 1978); CPC
International Inc. v. Train. 340 F. 2d
1320 (8th Or. 1978): FMC Corp. v. Tram.
539 F. 2d 973 (4th Of. 1978).
Unlike an-upaet—which is an
unintentional episode—a bypass is an
intentional aoncompiiance to
circumvent waste treatment facilities
during an emergency.
EPA has both upset and bypass
provisions in NPDES permits, and die
MPDES regulations- include upset and
bypass permit provisions. See 40 CFR
Part 122.4-1. 48 FR14151.14168 (April 1.
1983). The upset provision establishes
an upset as an affirmative defense to
prosecution for violation of technology-
based effluent-limitations. The bypas*
provision authorizes bypassing to
prevent loss of life, personal injury-, or
severe property damage. Since
permittees in the metal finishing
industry are entitled to the upset and
bypass provisions in NPDES permits.
this regulation need not repeat these
provisions. Upset provisions are also
contained in the general pretreatnaM
regulation.
XVTL Variance* and Modifications /
Federal and Slate NPDES permits to
direct dischargers must enforce these
effluent standards. The pretreatmem
limitations apply directly to indirect
dischargers.
The only exception to the BPT effluent
limitations is EPA'a "fundamentally
different factors" variance. See £ /.
dufont de Nemours and Co. v. Train.
supra: Weyerhaeuser Ca. i. Castle,
supra. This variance recognizes
characteristics of a particular discharger
in the category regulated that are
fundamentally different from the
characteristics considered in this
rulemaking. Although this variance
clause was set forth in EPA'a 1973-1978
industry regulations, it need not be _
included in this regulation. See 40 CFR
Part 123-30,
Dischargers subject to the BAT
limitations an also eligible for EPA'a
"fundamentally different factors"
variance. BAT limitations for
nonconventional pollutants may be .
modified under Sections 301(c) and
301(gj of the Act These statutory
modifications do not apply to toxic or
conventional pollutants; According to.
Section 301(j)(l|(B). applications for
these modifications must be filed wr&n
270 days after promulgation of final
effluent limitatiens«andr standard* See
43 FR 408S9 (Sept 13. 1978). These Part
413 and Part 433 regulations do not
regulate any non-conventional non-
toxic, pollutants. If any of the regulated
pollutants are declared non-toxic and
non-conventional in the future, then
dischargers may seek 301(cj or 30l(gJ
modifica tions*
Indirect dischargers subject to PSES
are eligible for the "fundamentally
different factors" variance and for
credits for toxic pollutants removed by
POTW. Sea 40 CFR 403.7; 403.13: 49 FR
9404 (January 28. 1981). Indirect
dischargers subject to PSNS are only
eligible for the credits provided for in 40
CFR 403.7. New sources subject to N5PS
are not eligible forEPA's
"fundamentally different factors"
variance or any statutory or regulator-.
modifications. See £ /. dufont de
Nemours v; Train, supra.
. Implementation of UmitadiMM
and Standards
A. Relation to NPDES Permits.
The BPT, BAT. and NSPS in this
regulation will be applied to individual
metal finishing plants- through NPDES
permits issued by EPA or approved
State agencies under Section 402 of the '
Act The preceding section of this
preamble discussed the binding effect of
this regulation on NPDES permits. -
except when variances and
modifications are expressly authorized.
This section adds more detail on the
relation between this regulation and
NPDES permits.
EPA has developed the limitations
and standards in this regulation to cover
the typical facility for this point source
category. In specific cases, the NPDES
permitting authority may have to
establish permit limits on toxic
pollutants that are not covered by this
regulation. This, regulation does not
restrict the power of any permit-issuing
authority to comply with law or any
EPA regulation, guideline, or policy. For
example, if this- regulation does not
control a particular pollutant, the permit
issuer may still limit the pollutant on a
case-fey-case basis, when such action
conforms with the purposes of the Act
la addition, if State water quality
standards or other provisions of State or
Federal law require limits on pollutants
not covered by this regulation (or
require more stringent limits on covered
pollutants), the permit-issuing authority
must apply those limitations.
3. Indirect. Dischargers
• For indirect dischargers. PSES and
PSNS are implemented under National
Pratteatment Program procedures
outlined in 40 CFR Part 403. The table
below may be of assistance in resolving
questions about the operation of that
program. A brief explanation of some of
the submissions indicated on the table
follows:
A "request for category determination
request" is a written request submitted
by an indirect discharger or its POTW,
for a certification on whether the
indirect discharger falls within a
particular subcategory listed in a
categorical pretreatment standard. This
assists the indirect discharger m
knowing just which PSES or PSNS limits
it will be required to meet See 40 CFR
403.8(a).
A "request for fundamentally different
factors variance" is a mechanism by
which a categorical pretreatment
standard may be adjusted, making it
more or less stringent on a case-by-case
basis. 0 an indirect discharger, a POTW.
or any interested person believes that
factors relating to specific indirect
discharger are fundamentally different
from-those factors considered during
development of the relevant categorical
pretreatment standard and that the
existence of those factors justifies a
different discharge limit from that
specified in the categorical standard.
then they may submit a request to EPA-
for such a variance. See 40 CFR 403.13.
395
-------
Federal Register /'Vol. 48. No. 137 / Friday. July 13. 1983 / Rules and Regulations 32475
A "baseline monitoring report" is the
first report an indirect discharger must
file following promulgation of a
standard applicable to it The baseline
report includes: an ^identification of the
indirect discharger a description of its
operations: a report on the flows.of
regulated streams.and the-result* of
sampling analyses to determine levefo of
regulated pollutants m those streams: a
statement of the discharger's
compliance or noncampiiance with the
standard- and a description of any
additional steps required to achieve
compliance. See 40-CTR 403.12(b)
A "report on compliance" is required
of each indirect discharger within 90
days following the date for compliance
with an applicable categorical
pretreatment standard.-The report must
indicate (he nature and concentration of
ail regulated pollutants is the facility's
regulated process wastestreams: the
average and maximum daily flows of the
regulated streams: and a statement of
whether compliance is consistently
being achieved, and if not what
additional operation and maintenance
and/or pretreatment is necessary to
achieve compliance. See 40 CFR
403.12(d)
A "periodic compliance report'" is a
report on continuing.compliance with all
applicable categorical pretreatment
standards. It is submitted twice per year
[June and December) by indirect
dischargers subject to the standards.
The report shall indicate the precise
nature and concentrations of the'
regulated pollutants in its discharge-to
the POTW; the average and maximum
daily flow rates of the facility; the
methods used by the indirect discharger
to sample and analyze-the data, and a
certification that these methods
conformed to those methods outlined in
the regulations. See 40 CFR 403.12(ej
TABLE 2.—(NOIRECT DISCHARGERS SCHEDULE FOR SUBMITTAL AND COMPLIANCE
Oiwor am
ptnoo
(tarn suaimffta to
P«au««t tor emaoir MM*
of santf-1
[ in * Ann aamaa on i
coma* Canvat
BCuiniiimiii niuur...i
1 Oiraaer « at CtMf wiimumuw OfHMr q» •. Warn <*mM* pqtmnon eamrai aMney VMR «n moron M prwri.iCB.tnto
or a» £P* A^onl W««r Qtviwon Qnctor. rf SUM oo-n not n«M «> MffO^tu^MBiMiH orogram
1 Control Autnamy * «) POTW it
-------
32478 Federal Register / Vol. 48. No. 137 / Friday. July 15. 1983 / Rules and Regulations
The compliance dates (or the two
categories are presented in Table 4. 3PT.
SAT. PSNS. and NSPS compliance dates
are specified by the Clean Water Act.
The compliance dates for Electroplating
PSES were set in the Federal Register on
September 28.1982. See 47 FR 42898.
Today's regulation allows facilities 3
years to comply with the Electroplating
PSES for toxic organics consistent with
the Settlement Agreement with NAMF.
For metal finishing, the Agency is
allowing 31 months for compliance with
all parameters. In addition an interim
TTO limit has been established for
compliance by June 30,1984; except for
metal finishing wastewaters from plants
which are also subject to Part 420 (iron
and steel), which must comply by July
10; 1985. This last exception is pursuant
to a settlement agreement with the steel
industry in which SPA agreed that
pretreatment requirements would apply
to steel discharges in luly 1985. It is '
passible that control of TTO in metal
finishing waste streams could, in some
cases, lead steel facilities to install
treatment technology on the discharge
from their steel processes. Therefore.
EPA has decided to allow plants
covered by Part 420 until June. 1985 to-
comply with the TTO limit
TABW 4.—COMKMMCS Ores
MM* =*•«••) PSES H*
i, CVMVW mq TTO. i
1 Par 91MB FaaMMB «• *w TTO am i«
D. Enforcement
A- final topic of concern is the
operation of EFA's enforcement
program. This was an important
consideration in developing this
regulation. EPA deliberately sought to
avoid standards which would be
exceeded by routine fluctuations of
well-designed and operated treatment •
systems. These standards were
developed so as to represent limits
which such a plant would.meet
approximately 99% of the time.
The Clean Water Act is a strict
liability statute. EPA emphasizes.
however, that it can exercise discretion
in deciding to initiate enforcement
proceedings (Sierra Club v. Train. 557 F.
2d 435, 5lh Or.. 1977). EPA has
exercised, and intends to exercise, that
discretion in a. manner that recognizes
and promotes good-faith compliance.
XIX Summary of Public Participation
-At the time of publication of the
proposed metal finishing regulation .
(August 31.1982). EPA solicited
comments on the proposed rules and. in
particular, an six specific issues. Ninety-
one cammenten responded to these and
other issues relating to the electroplating
and metal finishing standards. The
following parties submitted comments:
Air Transport Association of America
Alpha Industries Inc.
The Aluminum Association incorporated
• American Airlines
American Fouadrymen's Society
American Hoc Dip Galvamzen
.American Metal Stamping Association
Anorock Corporation
Anaconda Aluminum Company
• Ansul Fire Protection
Apollo Metala. Inc.
American Telephone-and Telegraph
Company
Atwood
Sabcoek and WUcox
3ausch•
PEC Industries
Pioneer Metal Finishing. Inc.
Porcelain Enamel Institute
Porcelain Metals Corporation
Praegttzer Industries inc.
Raytheon Company
Republic Airlines
Raxnora ,
Reynolds Aluminum
Rockford Area Chambers of Commerce
R.8. Donnelley and Sons
Sanders Associates Inc.
Sanitary District of Rockford
Sperry Corporation
Square 0 Company
State of Connecticut Department of
Environmental Protection
State of Vermont Agency of Environmental
Conservation
State of Wisconsin Department of Natural
Resources
United Airlines
397
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DIALOG F11e4I Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 46 of 69) User23913 23junfi2
cr*
K)
78-O5459
An In-depth, cross-flow separation technique for the removal
of suspended solids from wastewaters.
Sundararo. T. R. ; Santo. J. E. ; Shaplra. N. I.
HydronautIcs, Inc., Applied Science Dept.
INDUSTRIAL WATER ENGINEERING 15(1), 9-1O, 12-18,
Coden- IWEGAA Publ.Yr- Jan.-Feb. 1978
11lus. refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Results are presented from smalI-scale tests on the
microf111rat Ion of a variety waste effluents utl1 I zing
microporous tubes (Hydroperm), developed by Hydronaut tcs,
Incorporated. These thick-walled, tubular microfliters, which
can be made from many common thermoplast tcs (such as
polyethylene and nylon), enable almost the total removal of 5S
even at very low (about 5 ps1) filtration pressures. The
unique feature of the tubes Is that their pore structure can
be controlled during the production process; thus, optimum
fII trailon performance Is obtained for different waste
effluents by tailoring the tubes to the characteristics of a
given effluent under cons tderat ton, through a serles of
systemat1c. laboratory screening tests. Some results on
dewaterfng of waste sludges produced as an end product of
other treatment methods like dissolved air flotation are also
described. The filtration technique Is also capable of heavy
metal removal from waste streams provided that the metals can
be precipitated .in the hydroxide form by 1 1me addition or by
some other approprlate chemical treatment. Tests with
battery-waste effluents containing 7 to 8 ppro Pb Indicated
that the Pb level In the permeate was reduced to O.O18 ppm. <
AM)
DescrIptors: Suspended sol Ids; Effluent treatment; Pollutant
removal; F11trat ton; Industrla! effluents; Heavy metals;
Sludge dewatering; F11ter media; Engineering; FlIters;
HydraulIcs
I dent iflers: Hydroperm
acid mine drainage (AMD) converts the sulfate on the resin to
the monovalent blsulfate ion, freeing a resin exchange site
which may then be occupied by another an Ion. At Sml th
Township, a strong-acid cat ion exchanger Is coupled to the
Sul-bISul anIon exchanger. The effluent from the cat Ion
process-chiefly sulfurIc acId (H2SO4)- Is treated by the an I on
column to remove the free mineral acid of the AMD and the end
product, af ter chlor1natIon, meets potable standards. The
Desal process Incorporates a weak-base an ion exchange res In
which operates In the bicarbonate form to convert metal
sulfates to their bicarbonates, capable of being precipitated
by Al and Fe+3. Lime treatment removes the remaining cations,
except Na. Another process uses 2 res Ins-an H+-form,
strong-acid cation exchanger, and a weak-base anIon exchanger
In the free-base (OH-) form. In the cation column, H+ are
exchanged for the metal Ions of the AMD, leaving the cation
effluent predominant1y H2SO4 wlth res idual concentrat Ions of
metals. The effluent then enters the weak-base anIon
exchanger, where the acid Is absorbed by the resin. As the
anlon effluent contains residual levels of Fe and Mn. It Is
1 line-neutral ized to pH 9- 1O, f 11 tered, and adjusted to
neutrality. Either hydrochloric acid or H2SO4 may be used to
regenerate the cation column, producing a waste stream of
excess H2SO4 and sulfates of Fe, Al, Na, Mn, Ca. and Mg.
Regeneration of the anlon exchanger Is effected with sodium
hydroxide, and produces a waste stream composed mainly of
sodium sulfate. (FT)
Descriptors: Mine drainage; ion exchange; Potable waters;
Pollutant removal; Chemical react Ions; Ions; Res Ins; Acidic
wastes; Wastewater treatment
Ident Iflers• Sul-bISul process; Desal process
78-O5378
Invest 1 gat 1 on of 1 on exchange treatment of ac Id ml ne
drainage.
Wllmoth, R. C ; Scott, R. B. ; Kennedy/ J. L.
EPA, Industrial Environmental Research Lab., ClnclnnattI. OH
45268
Seventh sympos1 urn on coa1 mIne dra1nage research
Louisville. Ky. Oct. 18-2O, 1977
Seventh symposium on coal mine drainage research: Papers
pp. 88-1O6 Publ.Yr: 1977
Publ: Washington, D.C. Nat ional Coal Assoc1at Ion
11lus. refs.
No abs.
Languages: ENGLISH
Doc Type CONFERENCE PAPER
In the SuI-blSul Ion exchange process, the sulfate form of a
strong-acid anlon exchanger is used. The acidic nature of the
-------
DIAIUG FUe41: Pollution Abstracts - 7O-82/Apr (Copr Cambridge ScI Abs) (Item 48 of 69) User239l3 23Jun82
U)
78 O5312
Quality and treatment of coal pUe runoff.
Cox, D. B ; Chu. T. -Y. J.; Ruane, R. J.
TVA, Div. of Environmental Planning, 246 4O1 Bldg.,
Chattanooga, TN 374O1
Third symposium on coal preparation Louisville, Ky. Oct.
I8-2O, 1977
Third symposium on coal preparation: Papers pp. 252-275
Pub I Vr: 1977
Publ: Washington, D.C, Natlonal Coal Assoclat ton
11lus. refs.
No abs
Languages. ENGLISH
Doc Type: CONFERENCE PAPER
The water quality of coal pile drainage Is affected by the
leaching of oxidation products of metallic suSfides associated
with the coal. Runoff treatment methods of 2 TVA plants (J
and E) are summarized. A rainfall-runoff relationship can be
used to estimate detention basin design and to calculate acid
loads to ash ponds. The pH of the drainage from the 2 plants
was simitar desplte a dlfference In the S content of their
coal supplies, but acidity was higher at plant J despite the
similar pHs. Concentrations of 70S were somewhat higher at
plant J; most of the dissolved solids were sulfates. Iron
concentrations at both plants are lower In range and mean than
values encountered by other Investigators; Mn levels were
comparable or lower to those found In previous work. Lead.
Ba. and Ti were low or below the limits of detection; most
trace element mean concentrations at plant J are 3-8 times as
high as those at plant E. Mercury concentrations exceeded.EPA
water qualIty criteria at both plants, while As and Se
exceeded criteria only at plant J. Other metal Ion
concentrations are below the limits of toxlclty. Transfer of
the drainage to an ash pond for neutralIzatIon and
precipitation appears to provide adequate treatment. (FT)
Descr iptors: Runoff; Wastewater treatment; Eleetrie power
plants; Water qualIty measurements; Coal; Storage; Leaching;
pH; Heavy metats; Precipitation
Identifiers: coal storage piles
metals, and suspended participates. At the Belpre Coal Dock
on the Ohio River. It was decided to treat the runoff by lime
neutralization, aeration, and settling of precipitated calcium
sulfate, metallic oxides, and hydroxides. From rainfall data
from a nearby weather station. It was determined that a
treatment rate of 45 gpm with a recycle of a portion of the
treated wastewater and sludge would produce the desired
effluent and sludge density from the runoff from the 7.5 acres
of the storage area. Runoff Is diverted to a 2O7,OOO-gal
equalization basin. It then flows Into the concrete treatment
sump where 2% 11me slurry is added on demand from a pit
controller. The treated water is pumped to a 79,OOO-gal,
2-compartment settling basin; the clarified water Is decanted
and discharged to the Ohio River. Both equalization and
sett I Ing basins are clay-1Ined to prevent seepage Into
groundwater. To create a denser sludge, a portion of the
naturalized wastewater Is diverted back to the Inlet of the
treatment sump. A sludge density of 3O%-4Q% is thus obtained.
At power plants, the sludge Is burned with the coal. final
effluent from the runoff treatment has a pH of 6.5-7.5. U1
mg/l Fe, greater alkalinity than acidity, and J2O mg/1 TSS.
In a similar facility handling western coal, only SS need be
treated. The system consists of primary sett)ing and
collect ion ponds, a chemical trea tment uni t to add alum
coagulant, and a 2-compartment settling basin. (FT)
Descr iptors: Runoff; Wastewater treatment; Coal; Storage;
NeutralizatIon; SedlmentatIon; Set11 Ing basins; Sludges:
Prec ipltat Ion
Identifiers, coal storage piles; storm water runoff
78-O53I1
Treatment of precipitation runoff from coal storage plies.
Ferraro. F. A.
Amerlean Electr tc Power Service Corp., Environmental
Engineering Division. P.O Sox 487. Canton. OH 447O1
Third symposium on coal preparation Louisville, ky. Oct.
1S-2O, 1977
Third symposium on coal preparation. Papers pp. 243-251
Publ Yr; 1977
Publ. Washington. O.C Natlonal Coal AssoctatIon
11lus, no refs.
No abs.
Languages. ENGLISH
Doc Type: CONFERENCE PAPER
Precipitation runoff from coal storage piles can produce
was tewater conta in ing object ionable amounts of ac tdi ty.
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DIALOG FI1e4t: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item SO of 69) User23913 23Jun82
CT*
78-O45O7
Physical-chemical unit operations for the treatment of wood
preserving wastewaters.
Aver 111, D W.; Schmidtke. N. W. ; Netzer, A.
Fisheries and Erw trorwnent Canada, Environmental Protection
ServIce, Wastewater Technology Centre, P.O. Box 5O5O,
Burlington, Ont, L74 4A6, Can.
Technology transfer seminar on the timber process Ing
Industry Toronto, Ont., Can. Mar. 1O-11. 1977
Techno1ogy transfer semInar on the tImber process i ng
Industry: Proceedings. In CANADA. WATER POLLUTION CONTROL
DIRECTORATE. ENVIRONMENTAL PROTECTION SERVICE REPORT SERIES.
ECONOMIC AND TECHNICAL REVIEW REPORT EPS 3-WP-78 - I pp.
63-IO7 Publ.Yr: Jan. 1978
t1lus. numerous refs.
No abs.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
The 3 elements of Wastewater treatment process design are
removal of pollutants which form unstable suspensions, removal
of pollutants which form stable suspensions, and removal of
pollutants In solution. Gravity separators remove 60%-9O% of
settleable and floatable materials and separate those
materials which are lighter and heavier than water. Dissolved
air flotation can remove N95% of free oil and some emulsified
oil. Granular media filtration removes N95% of free oil;
subsequent separation of oil and creosote from the backwash
water Is required. CoaguiatIon, followed by sedjmentation,
flotation, or filtration, removes about 95% of emulsified oil.
N9O% of COD, most of the pentachlorophenol, and some phenol.
Flotation and filtration require less land area than
sedimentation. Flotation may be more effective for
thickening. Filtration requires a separate backwash storage
and separation tank If the backwash water Is not returned to
the head of the plant and clarified In the separator. Heating
Is ef fect1ve for treatment of water In oil emuIs ions by
evaporation. Chemical reduction and precipitation can produce
total residual metal ton concentrations 01 mg/1. Chemical
ox 1da 11on and precIp11a 11on can produce res IduaI As
concentrations O.5 mg/I. Chemical oxidation removes phenol
and pentachlorophenol. Adsorption on activated carbon can
result In effluent concentrations 01 mg/1 for many Wastewater
const 1tuents Including phenol and pentachlorophenol.
Adsorption requires a relatively high degree of pretreatment
to prevent fouling of the carbon surface. Solvent extraction
can remove phenol and pentachlorophenol from wastewaters, and
provide the potential for direct reuse of reclaimed
pentachlorophenol. (MS)
Descriptors: Physlcochemlcal treatment; Lumber industry
wastes; Industrial effluents; Effluent treatment;
Sedimentation; Flotation; Coagulation; FlItratIon; Reduction;
Chemical ox IdatIon; AdsorptIon; Sol vent extract Ion; Act Ivated
carbon; Oils; Organic compounds
Ident 1flers: wood preservat ives; phenols
Treatment of plating wastes from the automotive Industry.
Cullinane, M. 0., Jr.; Otetz, J. D.
Clark, Dletz and Assoc.-Engineerse Inc.
INDUSTRIAL WASTES 24(2). 29-32, Coden• INWABK
Publ.Yr, Mar.-Apr. I97B
t1lus. no refs.
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Wa ter conserva t i on measures recommended for a Mtsstsst pp t
plant Include using spring-loaded shutoff nozzles on water
hoses, collecting and returning steam condensate for boiler
water makeup, us Ing recycled water In the buff ing process, and
using counterflow rinsing in the plating operation. Several
Wastewater segregation practices were also recommended. To
meet federal standards, the most cost-effecttve effluent
treatment was reduct ion followed by chemical precipi tat ion.
Complete treatment and direct discharge was more cost
effect tve than pretreatment and discharge to the municipal
waste system. The optImum rInse system 1s a modifled
countercurrent system with 5 rinse tanks, which reduced water
consumption from K4OO gpm to J6O gpm. Features incorporated
In the treatment design Include addition of an acid feeding
system for raw waste pH adjustment and use of the abandoned
oxidation pond to equalize shock loadings. The treatment
process included the following: reductIon of Cr+6 in a
contInuous flow system; equalIzatIon of flow wastes; raw waste
pumping; pH adjustment tn a flash mix tank; and coagulation
and settling In a reactor-clarIfier. Provision is made for
future addition of filters and final pH adjustment. Vacuum
filtration and landfill Ing is the chosen method of sludge
disposal. Problems since plant startup in March 1977 have
been minimal. Water consumption could be reduced a further
4O%-5O% If recycle systems and more strIngent water
conservation measures were used, but these measures do not
appear to be economically justified at the present. (FT)
Descr tptors: MissIssIppi; Automot ive industry wastes; Metal
fInIshIng 1ndus try was t es; ChromIurn compounds; Wa t er
conservat ion; Wastewater treatment; Wastewater treatment
plants; IndustrIa I effluents; Reduct ton; CoagulatIon
78-O4471
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DIALOG FHe41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Scl Abs) (Item 52 of 69) User23913 23JunB2
U>
O^
Ui
78-O4274
Application and determination of organic polymers.
Wang. L. K.; Wang. M. H.; Kao, J-F.
Stevens Inst. of Technology„ Castle Pt. Stat 4on, Hoboken. Nvl
O7O3O
WATER, AIR. AND SOIL POLLUTION 9(3), 337-348. Publ.Yr:
Apr. 1978
t1lus. numerous refs.
Abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Varlous app)(cat tons of water-soluble and water-dlspers1ble
polymers In the f 1 elds of environmental, chemical„ and
blomedical engineering are reviewed. Catlontc electrolytes
are powerful primary coagulants because the colloidal matters
In natural systems are generally negatively charged. They can
be used not only for water purification and sewage treatment
but also for oil-water separatIon, corrosion control,
flocculatIon of Fe-ore siIroes, Improvement of 1Ime
precipitation processes, clarification of titanium sulfate
liquor, removal of heavy metals, killing of viruses, dredging
treatment„ and Industr1a1 wastewater treatment. In water
qualIty control. nonIonic polymers usual 1y functIon s
coagulant aids. coating the floe particles so that when flo s
collide, they adhere and form larger masses. Anton polyme s
are negatively charged and In the water softening proces .
where precipitation particles are positively charged, c n
function as primary coagulants. In general. In the tttratlon
of cat Ionic polyelectrolytes, polyvlnyI-sulfur1c acid
potassium Is used as a standard tItrant. The cat tonic
polyelectrolyte shows a light blue color In the presence of
Toluldlne Blue O dye (TBO), and the blue color turns bluish
purple at endpotnt. in the tttratlon of antonic electrolytes.
t,5-dimethyl -f,5-dlazaundecamethylene polymethobromlde Is
used, and the antonic polyelectrolyte shows a bluish color In
the presence of TBO, which turns light blue at endpotnt. (FT)
DescrIptors: Polymers; AnIons; Cat Ions; Wastewater treatment
; Water treatment; Coagulants; Water polIutIon control;
Chemleal analysIs
Identifiers: polyelectrolytes; Toluldlne Blue 0
coal gas IfleatIon, coal gas IficatIon. f Ixed-bed coal
gasification, and the COGAS process; reclaimed rubber by
high-speed commlnutIon; aerosol removal by sound wave
bombardment; drinking water purification by adsorption; Hg
recovery by chemical treatment; fluegas treatment for
sulf1te-pulplng boilers by scrubbing; heavy metal removal from
waste by sulflde precipitation; nuclear waste disposal by Ion
exchange and by vitrification; odor abatement In kraft pulp
mills by In-dlgester oxidation; participate removal from flue
gas by electrostatic precipitation; sludge drying by toroidal
dryer; solvents recovery; sulfate removal from 11 tan turn ox tde
waste by flocculatlon and by neutralization; sulfur dioxide
removal from stack gases by membrane electrodfalysIs and by
scrubbing; trInItrotoluene removal by surfactant treatment;
vapor recovery by carbon adsorption; waste Incineration by
molten-salt combustion; wastewater purification by biological
treatment; wastewater sterilization by oxygenatlon. carbon
adsorption. and Irradiation, and by UV oxidation; bleached
pulp by nonsulfur pulping; coal combustion by flutdlzed bed;
flue gas conditioning by sulfur trIoxtde generator; river
oxygenation by boat mounted O2 separation plants; and reverse
osmosIs by membrane. Several other processes Involving
Inorganic chemicals, metals, organic chemicals, petroleum and
fuels, plastics, etc. are discussed. (SS)
Descriptors: Technology; Chemicals; Petroleum; Fuels; Coal
gas f f teat 1on; Industrial plants; Air pollut ion control; Water
pollution control
78-O3975
New processes and technology alert.
Anonymous
CHEMICAL ENGINEERING 85(2), 141-151. Coden: CHEEA3
Publ.Yr: Jan. 16, 1978
no refs.
Sum.
Languages. ENGLISH
Doc Type: JOURNAL PAPER
The user, features, current status, and salient remarks are
tabulated for the following new products and processes:
ammonium sulfite from flue gas desulfurtzatIon; carbon black
from high temperature pyrolysIs of tIres; automotIve
lubrication olI reclaimed by solvent extract ton and
distillation; synthetic natural gas produced by fluId I zed beet
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DIALOG Flle41: Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Sc I Abs) (Item 54 of 69) User239l3 23Jun82
LO
01
CTi
78-O333I
Sodium bicarbonate helps metal plant meet Federal standards.
Barber, N. R.
and Dwight Co.
Inc.
P.O. Box 369 Piscataway. NJ
29. Coden: INWABK
26.
Church
O8854
INDUSTRIAL WASTES 24(1).
Publ.Yr: Jan. -Feb. 1978
H I us . no ref s .
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Treatment of toxic metal wastes with sodium bicarbonate
(NaHCO3) precipitates the metals and holds the pH at optimum
level. The treatment appears to be cost-effective, based on
theoretical studies of metal precipitation with hydroxides and
carbonates. Although NaHC03 Is not as efficient In removing
metal from solution as some other bases, it has the advantage
of neutralizing excess acidity and thus helps meet wastewater
discharge standards. The use of NaHCO3 In place of lime
eliminates many of the problems associated with the handling
and application of lime. Since the NaHC03 acts as a buffer to
maintain alkalinity near the optimum level, treatment plants
can be of a simpler design. Because this buffering action Is
automatic, there Is no need for complicated pH measurement and
application control systems. In small to moderate size.
systems, a dose of bicarbonate once or twice a day should
maintain pH at optimum levels for metal precipitation.
Although NaHCQS treatment does not precipitate all metals It
can be mixed with a suitable carbonate to Increase Its range.
A principle advantage of the bicarbonate-carbonate mixture Is
that It can be used to maintain an optimum pH over long
periods of time despite varying levels of effluent pH and of
metal In the effluent For Industrial plants In the 2OO.OOO
gpd-5OO.OOO gpd range, bicarbonate treatment systems may be
cost-effective (FT)
Descriptors: Metals; Wastewater treatment; Industrial
effluents; Precipitation; Effluent treatment; Chemical
treatment
Identifiers: sodium bicarbonate
regulations and the local municipal sewer code. Another
Hussong/Couplan System employing sphagnum peat as the
treatment medium can readily be tied Into the existing system.
In a series flow arrangement, at a later date. Changing
conditions can be met without costly, extensive replacement or
modification of the present system. The Hussong/Couplan
System treats the wastewaters with ferric chloride (FeC13) and
sodium sulflde (Na2S) at a pH In the 5-7 range In such a way
as to obtain a specific molar ratio of Cr6+6, FeCI3, and Na2S
In the effluent. A massive precipitate Is formed which
carried down virtually all of the Cr, both hexavalent and
trtvalent. The system at the Al plant Is a 6.OOO gpd system
and Is composed of 3 holding-batch tanks. chemical adders.
misers, controls, and sensors. To Insure the continuing
purity of the discharge, colorlmetrlc checks are made at the
precipitation tank. (FT)
Descriptors: Chromium; Aluminum; Metal industry wastes;
Effluent treatment; Industrial effluents; Precipitation;
Contaminant removal
Identifiers: Hussong/Couplan Treatment System
Coden: INWABK
78-O333O
Aluminum manufacturer removes chromium.
Anonymous
INDUSTRIAL WASTES 24(1). 24. 34.
Publ.Vr- Jan.-Feb. 1978
11lus. no refs.
No abs
L anguages: ENGLISH
Doc Type: JOURNAL PAPER
A New Hampshire aluminum company installed a Hussong/Couplan
Chrome Removal Treatment System to treat its raw effluent.
The effluent contains 164 mg/l total Cr. 136 mg/l hexavalent
Cr, 62O mg/l total P. and 22.8 mg/l Al. The decision was
based on 2 factors. The system reduced the pollutants to the
lowest concentrations In the final effluent and met, by a
comfortable margin. the requirements of the final EPA
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DIALOG Flle41 Pollution Abstracts - 7O-B2/Apr (Copr. Cambridge ScI Abs) (Item 56 of 69) User239l3 23jun82
3244
Ul
CTi
78-O3235
The distribution of heavy metals In anaerobic digestion.
Hayes. T. D.; Thels. T. L
Cornell Univ.. Dept. of Agricultural Engineering. Ithaca, NY
I485O
WATER POLLUTION CONTROL FEDERATION. JOURNAL 5O(I). 61-72.
Coden: JWPFA5 Publ.Yr: Jan. 1978
Illus. refs.
Eng.. Fr., Ger., Port.. Span, abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
Bench scale anaerobic digesters using municipal wastewater
sludge were dosed with different levels of heavy metals (Cr+3,
Crt6. Cd. Cu+2. Nl, Pb, and Zn) to determine their
distribution and note their effects under operating
conditions. Doslngs were made In both a stepulse and pulse
manner. Characteristic responses observed during periods of
digester distress Included Increased volatile acids and total
organic carbon. decreased gas production 'and methane
composition, and depressed values of pH. The order of
toxlclty established In this study was NIK CuKPbKCr(6|Cr+4KZn.
Toxic limits for Cd were not reached. Metals were rapidly
removed from digester supernatant In excess of 95%. The total
Insoluble portion was divided between Inorganic precipitates
and the blomass fraction Between 3OX and 6O% of the metals
were associated with the bacterial .cells. Toxic effects
became apparent at or near the maximum metals taken up1 by the
digester component. (AM)
Descriptors: Anaerobic process; Sludge digestion;
Distribution; Chromium; Copper; Cadmium; Nickel; Lead; Zinc;
Municipal wastewaters; Pollutant removal; Heavy metals
acid and a weakly basic anlon exchange resin after an
activated carbon filter, followed by a strongly basic anlon
exchanger. At the near neutral pH value of the wastewater
made possible by this system, complex cyanides are not
precipitated nor cyanide gas produced; free cyanide which
passes the mixed bed exchanger Is caught by the strongly basic
exchanger. Regeneration water and deteriorated bath are
treated with sodium hypochlorlte and ferric sulfate. Chromium
(III) Is treated with other cations with a strongly acid
exchange resin; hydrogen chromate and chromate Ion are treated
with other anIons by weakly basic exchange resins. Wastewater
containing heavy metals other than cyanide and Cr Is treated
by coagulation and sedfjnentat Ion, sand filtration, and chela te
resins which adsorb the metals selectively In series. (FT)
Descriptors: Wastewater treatment; Cyanides; Metal finishing
Industry wastes; Chromium; Heavy metals: Ion exchange;
Industrial effluents; Resins
78-O2S6O
An experience on re-use of waste water discharged from metal
plating shop.
Mural, V.; Yamadera, T.; Koike, ¥.
Hitachi Plant Engineering & Construction Co., Water & Waste
Water Treatment Dlv., Tokyo, Japan
International Congress on Desalination Tokyo, Japan Nov.
27-Dec. 3. 1977
Proceedings of the International
and Water Reuse: Vols. I and 2
97-1O4, Coden: DSLNAH Publ.Vr
Illus. refs.
No abs.
Languages ENGLISH
Doc Type: CONFERENCE PAPER
Conventional treatment processes for metal plating
wastewaters consist of oxidation, reduction. and
coagulation-sedimentation for both rinsing water and used
bath. Such treatment does not satisfy recent municipal
regulations A new process treats rinse water, containing the
bulk of cyanide and Cr wastes, with Ion exchangers; acid or
alkaline wastewater Is treated by chelate resin after
coagulation-sedimentation. The treated water can be returned
to the shop. The mixed bed exchanger consists of a strongly
Congress on Desalination
In DESALINATION 22(1-3),
Dec. 1977
-------
DIALOG F11e4l' Pollution Abstracts - 7O-82/Apr. (Copr Cambridge Sc I Abs) (Item 58 of 69) User23913 23jun82
U)
oo
78-O2557
RO applications In wastewater reclamation for re-use.
Sato. T.; Imaizuml, M.; Kato, 0.j et a).
Kurlta Water Industries, Japan
International Congress on Desalination Tokyo, Japan Nov.
27-Dec. 3. fl977
Proceedings of the International Congress on Desalination
and Water Reuse: Vots. 1 and 2. In DESALINATION 22(1-3),
65-76, Coden: DSLNAH Publ.Yr: Dec. 1977
11lus. refs.
Sum.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
The operation of a 37O-m3/d RO plant using ROGA spiral-wound
modules to treat metal plating wastewater for reclamation 1s
described. To facilitate achievement of 92% recovery. sodium
hydroxide was substituted for calcium hydroxide In the primary
neutraltzatIon stage, prevent Ing precipitation of calcium
sulfate on the membrane surface. The RO feed Is measured by
filtration time and color. A nonionic polyelectrolyte with
ferric chloride Is used for coagulation and clarffIcatton.
followed by gravity type dual layer filtration at a velocity
of 8 m/hr. TDS in the RO permeate are J1O% that of the RO
feed. The permeate Is further demtnera)fzed by Ion exchange.
Brine COO is removed t>y an activated carbon filter. and heavy
metals are adsorbed by Ion exchange resins. Backwash wastes
from f11ters and regenerat ion wastes from the heavy metal
removal unit are recycled to the neutralization tank. The
membranes are chemically cleaned once or twice a year; over 18
mo, the flux decline has been very slight. In a RO plant for
etching process wastewater. coagulation is with polyalumtnum
chloride, with further pretreatment by gravity type dual-layer
filter, polIshlng sand filter, and 2O-I safety filter.
Permeate water quality Is 78 ppm TDS. compared to I.2OO pprn In
the feed water. The product water Is used for rIns Ing
purposes. Another RO plant treats laboratory wastewater.
Water recovery Is 9O%, Water reclamation from brine wastes Is
made by an evaporation process, so that overall water recovery
1 s 97%,- 98%. Recovered wa ter Is used for blot og 1 ca I
experiments and cooling towers. (FT)
Descriptors; Japan; Reverse osmosis; Industrial effluents;
Wastewater treatment; Wastewater treatment plants; Metal
f in Ishing industry wastes; Water reuse
Sum.
Languages: ENGLISH
Doc Type: CONFERENCE PAPER
A Jar Based Batch Settling Test (JBBST) was used to evaluate
the performance characteristics of commercial polyelectrolytes
for use in the flocculatIon of domestic wastewater subsequent
to coagulat ion by a metal He coagulant. Performance
evaluation by the JBBST technique relies on the measurement of
floe settling rate which can be used to predict continuous
clarlfler effluent concentrations as a function of clarlfier
overflow rate. Thirty-two dlfferent commerclal
polyelectrolytes were examined initially by JBBST for domestic
waste water clarification and P removal in conjunction with
alum. A mid-range hydrolysis (1O%-2O%) anlonic polyacrylamlde
Is the most suitable polyelectrolyte for such applicat ion.
Extens 1ve tests were undertaken wlth dlfferent
polyelectrolytes, at severa 1 dosages and 2 dIfferent
wastewater plants. At all probablI I ties, the mid-range
hydroIys f s po\yacryI am t de Is super tor to the h igh percent
hydrolysis poI ye1ectrolytes usua11y recommended by
manufacturers for this application. (AM)
DescrIptors: Domestic wastes; Wastewater treatment;
Flocculat ion; Secondary treatment
Ident If iers: polyelectrolytes; comparatIve evaluatIon
78-O2522
Comparative evaluation of commercial polyelectrolytes for
flocculating alum precipitated domestic wastewater.
Benedek. A.; Banes I„ J. J.
McMaster Univ., Dept. of Chemical Engineer ing, Haml1 ton 16,
Ont. L8S 4L7, Can.
Eighth International conference on water pollution research
Sydney, Austral la Oct. 17-22. 1976
Eighth international conference on water pollution research.
Edited by S. H. Jenkins In PROGRESS IN WATER TECHNOLOGY 9(1)
32--I2, Coden PGWTA2 Publ . Yr. 1977
1 Ilus refs
-------
IALOG Flle41- Pollution Abstracts - 7O-82/Apr (Copr. Cambridge Set Abs) (Item 6O of 69) User239t3 23jun82
3246
U)
CTi
control of
Research
Coder.: ENFIAG Publ.Yr: Oct.
In
flue gas
sulfur
from pulverized
dioxide (SO2).
/8-O1987
Optimization of waste disposal systems in
environmental Impact of coal-fired utilities.
Breltsteln, L : Ellison. W.; Warner, M.; et al.
NUS Corp., Environmental Safeguards Division, 4
PI.. Rockvtlle, MO 2OB5O
COMBUSTION 49(4). 35-4O.
1977
i1lus. refs.
No abs.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The principal contaminants
coal-fired boilers are parttculates
nitrogen oxides (NOx). and smaller amounts of carbon monoxide.
hydrocarbons, aldehydes, and toxic trace elements. The
principal wastewaters from steam electric generating plants
are low volume waste, ash sluice, metal cleaning waste, boiler
blowdown, once-through condenser cooling water, cooling tower
blowdown, and materlal-storage and construction runoff. The
principal solid wastes are bottom ash, dewatered fly ash, and
flue gas desulfurIzatIon (FGO) sludge. containing dissolved
solids. COD. and trace elements. Cooling systems produce both
chemical and thermal wastes. FGD systems for SO2 control cost
$6O-$75/kw for a SOO-Mw plant. Participates are removed by
electrostatic preclpltators at a. capital cost of tS-$2O/kw.
Emission limits for NOx are now met solely through design
engineering. Effluents are brought Into compliance with 1977
regulations through neutralization, oil removal, mixing,
precipitation, flocculatIon. sedimentation, pH adjustment, and
settling. Systems may or may not be mechanical equipment
Intensive; costs will be S2-$B/kw generating capacity. The
1983 effluent requirements will necessitate Incremental
expenditures of $5-$15/kw for bottom ash sluice water and
$1-$2/kw for cooling tower blowdown. FGD solid waste
stabilization methods Include pug mill mixing and landfill
compaction of filter cake, dry fly ash. and other dry
additives. and feeding silicate additives to FGD slurry
discharge flow to pond disposal sites; capital costs are
$IO-$5O/kw. Cooling lakes and ponds, evaporative rectangular
mechanical draft towers, and hyperbolic natural draft towers
are used for cooling surface waters. Liquid and thermal
discharge control systems are highly site dependent. (FT)
Descriptors: Coal; Boilers; Industrial emissions; Industrial
effluents; Electric power plants; Thermal discharges; Cooling
systems; Federal regulations; Economics; Engineering: Solid
wastes; Flue gas desulfurIzatIon; Environmental Impact;
Pollution control
lllus. refs.
Sum.
Languages: ENGLISH
Doc Type JOURNAL PAPER
The most commonly used treatment for removal of fluorides
involves the addition of a soluble Ca salt, forming Insoluble
calcium fluoride. Effluents treated in this manner generally
have concentrations of fluorides from 12 to 3O mg/l. Any
fluoride that Is complexed will not readily react with a Ca
salt. The Ca salt must be present In enough quantity to
completely precipitate the soluble fluoride. The pH must also
be controlled to a range predetermined by experimentation.
usually between 8 and 9, or KI2. Factors affecting the
required pH range include the characterIsts of the waste
stream and the specific treatment process. Heavy metals and
fluorides may be removed simultaneously. Reaction times vary
from 3O mln to 24 hrs. Fluorides can be removed either by
batch treatment or by a continuous flow-through process.
Continuous treatment Is preferred for KIOQ.OOO gpd.
Continuous treatment typically utilizes an equalization tank.
a reaction tank, sludge-handling systems, and instrumentation.
A process flow chart for sludge handling Is provided and each
step of the continuous treatment procedure Is discussed.
Hydrofluoric acid solutions must be neutralized, usually with
lime, either prior to or at the same time as the precipitation
step. Aluminum sulfate (alum) has been used to lower F-
concentratIon and the efficiency of the alum flocculatlon
affects the extent removal. Alum treatment also Increases the
amount of sludge and results In thickening and mechanical
dewaterlng. The alum can possibly be recovered from the
sludge using the proper technology. Activated alumina can
reduce F- levels to J2 mg/l. Significant factors affecting
this process are discussed. (FT)
Descriptors: Fluorides; Industrial effluents; Wastewater
treatment; Pollutant removal; Aluminum compounds
Identifiers: alum preclpltat Ion
78-OI271
Reducing fluoride In Industrial wastewater.
Paulson, C G
Industrial Pollution Control, Inc., 46 Riverside Ave.,
Westpost, CT O688O
CHEMICAL ENGINEERING 84(22). 89-94, Coden CIIEEA3
PubI.Yr Oct. 17, 1977
-------
DIALOG F1te41 Pollution Abstracts - 7O-82/Apr (Copr Cambridge Scl Abs) (Item 62 of 69) User23913 23Jun82
UJ
-0
O
45 Riverside Ave. ,
Coden : CHEEA3
78-0127O
Heavy metals removal.
Lanouette, K H.
Industrial Pollution Control, Inc.,
Westport, CT O688O
CHEMICAL ENGINEERING 84(22). 73 -BO,
Pub) .Yr: Oct. 17, 1977
I I lus . ref s .
Sum.
Languages: ENGLISH
Doc Type: JOURNAL PAPER
The mos t common me t hod for the remova 1 of 1 nor gan I c heavy
metal s Is chemical prec (pi tat Ion. Typical f Inal concent rat Ion
level s are given for this method, and specif Ic treatment
methods are discussed. Including batch and continuous systems.
Batch treatment systems can be designed for flows JSO.OOO gpd
and usual ly consist of 2 tanks. When wastewater
characteristics are uniform or when large volumes must be
handled. a continuous system Is applicable. It Is best to
remove suspended heavy metals from the chemically treated
ef f Utent by f 1 1 trat Ion. Sludge hand I Ing may consist of
dewater Ing by centrifugal Ion, plate and frame f 1 1 ters, or
sludge-drying beds. Recovery of metals from sludges Involves
acid digestion. neutralization. and electrolysis. Chemical
precipitation of heavy metals Is usually accomplished with
lime, caustic, and sodium carbonate. Costs and procedures
involved with using these chemicals are considered. Alternate
removal methods are activated carbon adsorption, ton exchange.
reverse osmos Is. and cementat Ion. The aspects of each
procedure are discussed. Precipitation removal techniques for
Cd Include pH adjustment with lime or caustic to a pH of about
11. or with sodium carbonate to a pH of 9.5-1O. Hexavalent Cr
can be precipitated by adjusting the pH and adding a reducing
agent , usual ly sodium dlox Ide or r sodium metablsul f 1 te .
Trlvalent Cr is precltltated at a pH of 7.5 8.5 with time or
caustic. Other means for Cr removal Include activated carbon.
ion exchange, and biological treatment. Precipitation of Pb
with lime, caustic, or soda ash Is useful. Studies Indicate a
combination of trlsodlum phosphate and caustic is the most
effective system. Mercury Is precipitated by an acid pH
adjustment and the addition of sodium sulflde; separation Is
accompl (shed by f 11 trat Ion Silver is recovered by
electro) ys is and cementat Ion. Pr imary sources and spec! f Ic
treatments for each of the above metals are outlined. (FT)
Descriptors: Heavy tnetals; Industrial effluents; Pollutant
remova I ; Wastewater treatment ; Sludge treatment
su If Ides or elemental
system is out 1 Ined.
act Iva ted- sludge system
5- 1O mg/l was reported.
for a manufacturer of
Doc Type- JOURNAL PAPER
The advanced techniques of electrodlal ys Is . ion exchange and
RO now seem feasible for control of selected S-containlng
effluents and may become practical for recovery processes as
well. Biological treatment of 5 containing wastes may involve
either aerobic or anaerobic bacteria. For reduced forms of S.
aerobic treatment Is feasible, typically producing
thlosul fates or sot fates as the end products Anaerobic
treatment is appl 1 cable to ox Id I zed) forms of S to yield
S. The chemistry of each biological
Sat Isf actory operat Ion of an
with Inf luent S-2 concentrat Ions of
Biological waste treatment studies
textile chemicals and dyestuffs show
that highly variable S-2 levels (ranging from 1O to 65 mg/l In
the plant waste discharge) Inhibited biological treatment.
Aerobic biological treatment Is effect I ve only when the
Influent concentrations are relatively constant and sufficient
O2 for oxidation Is available. The primary end product of
biochemical ox 1 da t ion of thlosul fate Is sulfate (S04-2 ) ,
Biological treatment In a pulp and paper mill can remove K95%
of the S In wastewater containing K2OO mg/l of sulf Ite.
Anaerobic bacteria can remove S from wastes, but the reaction
generates disagreeable S-2 odors . Sul f ate concentrat Ions JtOO
mg/ 1 avo Id s t gn 1 f 1 cant S - 2 odor I n an anaerob i c 1 agoon .
Chemical treatment by oxidation or precipitation is effective.
Oxidation with 02. H20. C12. and other oxldants Is described.
Precipitation with heavy metals such as Fe. Zn, Pb. Ag, and Cu
Is an effective treatment method. Activated carbon adsorption
gained wide acceptance In general wastewater treatment and now
appears to be a v table method for remov ing S compounds .
Pro treatment wastewater to remove part leu la tes may be
necessary . ( FT ) *
Oescr 1p tors . Sul fur compounds ; Sul fur removal ; Wastewater
treatment ; Reverse osmos ts; Industr lal effluents; B lologlcal
treatment ; Chemical treatment ; Ion exchange
I dent if lers: sulf a tes; sul f Ides; sulf I tes; electro-dialysis
78-O1269
Controlling sulfur compounds In wastewaters,
Watklns, J. P
Hydrosclence, Inc . 363 Old Hook Rd.. Westwood. NJ O7675
CHEMICAL ENGINEERING 84(22). 61-65. Coden• CHEEA3
Publ.Yr. Oct. 17. 1977
11lus, refs
Sum
Languages ENGLISH
-------
Federal Register /• Vol. 48. No. 137 / Friday, July 15. 1983 / Rales and Regulations 32477
Whirlpool Corporation
York Metal Finishing Co.
The major issues raised by
commenters are addressed in this
section. A summary of ail comments
received and of our responses is
included in the public record for. this
regulation.
1. Comment: Many commenten
objected to the certification language-
EPA proposed as an alternative to TTO
Monitoring. One commenter pointed out
that EPA bad recently proposed new
certification language for signatories to
permit applications and reports (40 CFR
122.6) as part of a settlement agreement
in the consolidated permits litigation,
(NRDC v. EPA, and consolidated cases.
No. 80-1607. O.C. Or.) and suggested
that EPA adopt that language here.
Response: EPA agrees that changes in
the certification language are warranted.
First we believe it is appropriate to
modify the proposed- language to accord
more closely with the certification
language agreed to in the consolidated
permits settlement agreement
concerning 40 CFR § I2i22, formerly
§ 122.8. 47 FR 2S54B. 2SS33 (June 14,
1982). We do not see a significant
enough difference between this
regulation and § T.2Z2Z to justify
substantially different language. Thus.
we have adapted the proposed
settlement language with minor
differences reflecting the particular
nature of the TTO certification
requirement This language is
substantially similar to that now
available for the electrical and
electronics industry (Phase I). SSB 48 FR
15382. April 8.1983.
Second, we-have amended the
language to allow the diacnarger to
certify that "no dumping of concentrated
toxic organics into the wastewater has
occurred since filing the last discharge
monitoring report" The proposed
language appeared to require the
discharger to certify that lie is in
compliance with the limit: we recognize
that it may be difficult to certify to this
language in the absence of monitoring.
Now. the discharger will be allowed to
certify as-to his toxic organic
management practices. However.
because the new wording is less precise
(i.e.. no "dumping of concentrated toxic
organics"} and because some
commenters pointed to the need for
more specificity about certification
procedures, we are adding more explicit
language requiring the discharger to
describe his toxic organic management
plan. The proposed language would
have required the discharger to specify
the toxic organic compounds used and
the procedure used to prevent excessive
wastewater discharge of toxic organics.
whereas the final language requires the-
discharger to submit a toxic organic
management plan that specifies to the
permitting or control authority's
satisfaction the-toxic organic
compounds used: the method of disposal
used instead of dumping, such as resale.
reclamation, contract hauling, or
incineration: and procedures for
assuring that toxic organics do not
routinely spill or leak into the
wastewater. The discnarger must also
certify that the facility is implementing
the toxic organic management plan.
Finally, for direct dischargers, the
solvent management plan will be
incorporated aa a condition of their
NPOES permits. A similar requirement
does not exist for indirect dischargers
because under the Clean Water Act
permits are not issued for them by the
control authority. However, the
pretreatment standard does require
indirect dischargers to implement the
plan which they, submit to the control
authority. Both these requirements
reinforce the discharger's responsibility
to implement his certification statement
Addition of certification language is
intended to reduce monitoring burdens.
it does not in any way dinusfl.the
discharger's liability for noncompliance
with-the TTO limitation.
2, Comment: Several commenters
questioned EPA's estimate of minimal
costs for TTO control stating that-
signficant costs would be incurred from
solvent disposal and from compliance
monitoring. A number of commenters
questioned the statement that costs for
solvent disposal could be offset by
reclamation of these wastes.
Response: The Agency recognizes that
costs can bs associated with proper
solvent management* and compliance
monitoring. However." the. Agency does
not believe these costs will be
significant for the majority of the
facilities in the industry. 24% of the
captives. 10.3% of the job saops.and
100% of the printed circuit board
facilities perform solvent decreasing. An
estimated 73 percent of the facilities
using solvent decreasing are already
practicing proper disposal of these
wastes and would, therefore, not be
expected to incur additional costs to
comply with the electroplating or metal
finishing TTO limits. Facilities not
presently practicing proper solvent
management would need to implement
practices such aa contractor removal
and/or reclamation.
Costs of proper solvent disposal can
be offset by solvent reclamation. In
response to comments, the Agency
contacted representatives of national
solvent reclamation associations. These
representatives indicated that solvent
reclamation is a widespread, readily
available, and growing practice. In
addition to the numerous plants with on-
site reclamation facilities, it is estimated
that more than 100 independent
reclaimers are in operation throughout
the country and that reclaimers will pay
for spent solvents especially if the
solvents are segregated and there is a
market demand for the particular
solvents.
The Agency recognizes that frequent
monitoring for TTO can be expensive.
The Agency has attempted to reduce the
cost by establishing the certification
alternative and by allowing monitoring.
when.necessary, to be limited to those
toxic organics likely to be present in the
wastewater of a plant The Agency
believes that almost all facilities will be
able.to certify in lieu of monitoring.
However, in response to comments on
the cost of compliance monitoring, the
Agency has re-assessed its cost estimate
to consider quarterly monitoring for
TTO. This frequency is reflective of a
common monitoring frequency required
by control authorities. For the reasons
explained in section IX above. EPA
believes that its. economic analyses of
the impacts of the TTO limit are
conservative and fully state or overstate
the likely actual economic impacts.
3. Comment: Some commenters
pointed out that the new source limits
for cadmium were not supported by
historical performance data. However,
no commenten submitted data on
performance capabilities of new source
technology.
Response: New source standards for
cadmium are based on control
technology which is designed-to reduce
cadmium in wastewater discharge from
cadmium sources, e.g. cadmium plating,
chromating of cadmium plated parts.
and acid.cleaning of cadmium plated
parts. The new source standards for
cadmium are based on the amounts of
cadmium expected as a background
level to be found in wastewaters from'
plants not involved with cadmium
plating. The standards were determined
from data on concentrations observed in
untreated wastewater from metal
finishing plants that do not plate
cadmium. It represents the amount of
cadmium present from incidental
sources, when the principal cadmium
sources are full controlled. The data
consist o/ si observations from 27
plants. The data were divided into
statistically homogeneous groups by
plant. The average upon which the
standards were based was taken from
the group with the highest average
cadmium concentration. Estimates of
398
-------
32478
Federal Register / Vol. 48. No.. 137 / Friday, July 15. 1383 / Rules and Regulations
variability used in determining the limits
wen obtained from the two highest
groups.. This was somewhat
conservative, because precipitation/
clarification systems should achieve
significant tether removals from these
raw waste streams.
The Agency also cheeked the
consistency of th* limit with data from
EPA sampled precipitation/ clarification
systems. These data indicated that the
new source limit could be achieved
alternatively by using precipitation/
clarification, rather than total control, of
the principal cadmium source. Tail
review included plants with ca^nftinnft
raw wastes of from CLQ12 to, T-33 mg/L
The Agency also reviewed the data base.
used to develop the cadmium limit to
venfy that it 'm^idqd all available data
from lion-cadmium plating plants* Prior
to promulgation costs wen also re-
gxamined to fart™^ expenses for
control of nhmrnattng and acid cleaning
of nafftrfliiffi plated parts* in. iftdition to
rnntTnllinarfT^flyn^t^ plating whtcll Was
assassed-in the proposal.
4. Comment. Cj?niTnttn*ftrt suggested
various averaging times as the basis, for
monthly limitations. mi-lnrting 4-day. 30-
day. and "TP day averages.
Response: The Agency has evaluated
the merits of the suggested alternatives
and decided that an average of ten-
samples (obtained within, a one-month,
period) would provide a reasonable
basis for monthly limitations.
minimizing, the number of samples
necessary.
Although it is not anticipated that a
irntonng frequency or 10 times per*
month will always be required, the cost
of this frequency of monitoring is-
presented in the economic impact
analysis to the metal finishing
regulation. That frequency was selected
because if facilities sample 10 times per
. month they can expect a compliance
rate of approximately » percent if they
are operating at the expected mean and
variability, Plant personnel, in
agreement with the control authority.
may choose to- take fewer samples if
their treatment system achieves better
long- term concentrations at- lower
variability than the basis for the limits.
or if plant personnel are willing to
accept a statistical possibility of
increased violations. The 10 sample
monthly limit is consistent with other
regulations and recent proposals for
other metals industries, e.g« porcelain
enameling, coil coating, batteries.
copper, and aluminum forming.
The 4-day average is-an inadequate
measure of treatment system
performance over extended periods.
This basts was used forth*
electroplating rules only under the
special circumstances of a Settlement
Agreement.
The N-day average suggested by two
commenters was considered by the •
Agency but was rejected as
unnecessarily complex and likely to
create confusion for hath dischargers
and control authorities*
on the desirability or need to rescind the
electroplating regulations for captive
electroplates upon the compliance date
Response: The Part 413 Electroplating
PSES will no longer o* applicable to
captive electroplating when they must
comply with, the Metal Finishing PSES-
for metals and cyanide is reached.
Captive eiectroolaters will then b»
regulated under the Part 433 Metal
Finishing PSES. Then is no need to
maintain two sett of requirements for*
the same pollutants at th* same plants.
It for some reason. Part 433 should
become inapplicable, than Part 413 will
apply to them.
9. Commexrc TOM majority of
commenters responding to the question*
of- the PSES compliance data-stated that
March 30.1984 would not provide
sufficient tin* for compliance.
Response: To allow facilities
sufficient **m^ to i™q*gii or upgrad* th*~
necessary treatment systems, the
Agency is establishing the compliance'
date of th* Tmf*ai finishing omffi foe*
metals and cyanide-to be 31 months
from th* date of promulgation!. This
extension-is based on an-Agency study*
which showed that 31 months is-
required to planrdnign. and ^nft^Ji th*
reconu&flttded treatment technology.
This extension due* not apply ta
compliance with the-toxic organics limit
howeveg.Por Metal Finishing PSES. an
intenm.TTQ level must be achieved by>
Juna.20.138*. based on.no. und-of-pipa
treatment and th* final TTO limit based
on end-of-pipe treatment most be
achieved 31 months from the date of
promnlgaaon.FgrElecatipiating.PSES.
the TTO.cnoipliaiiea-dats.is 3 years from
promulgation, of this ruiemakaig. That
allow* th* joo- shop and £PC3M sectors-
the maarhmiitv allowable time-for
corapoaac* under the Clean Water Act
(CWA).
7. Comment: Commenten stated mat
the proposed lead limit was not
achievable based on the technology
recommended. Some argued that plants-
with high raw wast* lead values wen
not adequately represented in the data
base. One commenter submitted
additional data.
Response: The- Agency reviewed the-
lead data base to assure mat all usable
data from plants having a lead source
wen included. EPA did consider some
additional self-monitoring data that
were found to be applicable and
excluded data from an onginaHy-
considerad plant which was not
adequately controlling waatewaters. The
revised EPA data base was used to
derive a final lead limit. The daily
maximum for lead has been changed
slightly from OS7 mg/l to 0.89 tng/U The
Agency also examined data submitted
during the comment period. These data
were not included because of
inadequate treatment design and/or
operation. For example. TSS values as
high as 119 mg/l were submitted, oil and
grease was as high as 1395 mg/l and
hexavalent chromium was as high as
LJ3 mg/L An examination of the
possible ejract of including the
commeater's data for lead revealed that
only a-slight change in the limit would
hava occurred.
3. Comment: Some commenters
suggested a small plant exemption from
the Metal Finishing regulations, arguing
that an exemption should be granted
similar to that provided by Part 413 for
plants discharging less than 10.000
gallons per day.
Response: Small indirect discharging
facilities (<10.000 GTO discharge) were
given less stringent requirements in the
Electroplating Pretreatment Standards.
Many of these facilities are job shops
and for th* caasons stated above will
not be covered by the Part 433
requirements*
The Agency re-examined the effect of
the Part 433 metal finishing regulations
on small facilities; and. has determined
that because job shops and IPCBMs are
exempted from the metal finishing PSES
then would be- no significant economic
impacts if the remainder were covered
by the- metal figiahiflg standards. For
indirect captives discharging less than
10:000 GPD. the investment cost would
amount to S38 million with annual costs
of S12 million. There ars-no-estimated
plant-closure or divestitures. A small
facility exemption is not warranted for
the Metal Finishing regulation.
9. Comment: Some eonunenters stated
that tire-addition of a TTO limit, to the
Electroplating PSES is a violation of the
NAMF Settlement Agreement
Response: Under the March 1980
Settlement Agreement the Agency
agreed that:
any further SAT analog standards will b»
bued on tnatnat tecasaiogy compatible
with tiis modal teehnolxgy upon which these
stuujaaiM wwa baaed .... la developing
BAT analog standards for the industry. EPA
will lake into account the cumulative impact
of th«»« "UPP regulations in determining
what is "KonoaneaUy achievable." * ' ' As-
to thw jupuuni of the meta> finishing industry
399
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Federal Register / Vol. 48, No. 137 / Friday, July IS. 1983 / Rules and Regulations
32479
that u economically vulnerable. EPA does
not believe that more stringent regulations
are now economically achievable. Therefore.
EPA does not plan to develop more stringent
new pretreamem standards for the |ob shop
metal finishing segment in the next several
yean. Nor does EPA plan to develop in the
next several yean more stringent standards
for the independent printed circuit board
segment where significant economic
vulnerability also exists.
EPA is not imposing metals and
cyanide limitations more stringent than
those specified in the Part 413 existing
applicable pretreatment standards,
despite evidence that such limits can be
reliably-achieved by the technology that
forms the basis of the current standards.
Indirect discharging job_3hop and
independent printed circuit board
facilities are expected to incur costs
only to comply with the TTO limitation
which is being added to the
electroplating pretreatment standards in
Part 413. This TTO limitation is included
in the regulation because it will
substantially reduce a significant toxic
problem, while compliance will cause
negligible economic impacts on these
industry sectors. Compliance with the
toxic organic standard can be achieved
by good management practices (i.a.. not
dumping waste solvents into the
wastewaters). No additional end-of-pipe
technology (beyond that required for
metals removed) is necessary.
Even under very conservative
estimates only 77 of an estimated 2734
indirect discharging job shops and 88 of
the 327. indirect independent printed
circuit board manufacturers may incur
costs to comply with the TTO standard.*
Total annual costs for all plants of
S222.500 and S254.300 respectively are
projected for the two sectors. The
average annual cost per facility to
comply with the TTO limitations is
approximately $2900, primarily for
sampling and analysis. No closures or
employment effects are projected for
these sectors. Production cost increases
are expected not to exceed 0.03 percent
for the two sectors.
The economic impact analysis also
performed two sensitivity analyses: the
first with a greater number of plants "
monitoring and. the second, with plants
monitoring monthly instead of quarterly.
Both changes led to only slightly
different impacts. At most only one
plant would be affected. All scenarios
were found to be acceptable and
economically achievable. Thus the TTO
limits are not "more stringent
standards" in the sense of the
Settlement Agreement, which expressly
tied "stringency" to "economic
vulnerability".
Finally, the TTO limits need not be
complied with before 1988. Thus, even if
control of TTO were considered
significantly more stringent the time
allowed for compliance will amount to 3
years from the date of the Settlement
Agreement. That fulfills the Agency's
1980 obligation not to develop
significantly more stringent standards
for those facilities for the next several
years. :
10. Comment Some commenters
stated that the proposed TTO limit could
not be met using a combination of
solvent management and common
metals treatment. Several commenters
also pointed out that plants previously
in compliance-with the metals
limitations under'Electroplating PSES
may now require installation of common
metals treatment to meet the TTO limit
Response: The Agency has reviewed
the TTO data base, reevaluated the
mean and variability factor, and revised
the effluent limit for TTO. The major
factor contributing to the change was
the examination of the TTO levels at
certain groupings of plants. The most
notable discovery was that plants that •
performed both 30! vent .decreasing and
painting tedded to have the highest
background concentrations of any
process grouping. The limit has been
based on these plants. Where plants are
otherwise subject to a regulation whose
technology basis includes precipitation/
clarification for removal of metals, the
TTO. limit has been based on effluent
data from precipitation/clarification -
treatment systems. We have also
established'a TTO limit of 4.57 mg/1
based on only management practices.
This limit is. being used as an interim
requirement prior to installation of
pollution/equivalent to precipitation/' ,
clarification, and for plants discharging
less then 10.000 gpd and now covered by
the Part 413 Electroplating PSES. Thus
today's regulation specifies an interim
TTO limit for-small plants (<10,000
gallons per day)Jbecauae these plants
may not already have common metals
treatment in place. Furthermore, the
Agency notes that most facilities should
be capable of achieving compliance with
the ultimate TTO standard even without
end-of-pipe treatment, simply through
strict management control of toxic
organics. 89% of the TTO data prior to
and-of-pipe treatment would comply
with the final TTO limit baaed on the
inclusion of precipitation/clarification.
11. Comment: Several commenters
recommended an amenable cyanide
limit as an alternative to a total cyanide
limit because amenable cyanide more
accurately reflects the performance of
alkaline chlonnation treatment.
Response: Most facilities should be
able to meet the total cyanide limit.
However, sufficient information has
been presented on cyanide formulations
and formation of complexes to support
the possibility that a significant
population could fail to meet the
limitations. The technology basis is
alkaline chlorination which destroys
amenable cyanides. Thus, the final rules
include an alternative cyanide limit for
plants generating significant quantities
of complexed cyanide. The data and
basic calculations for the alternative
cyanide limit were presented in the
proposed development document The
Agency rejected specifying a limit only
for amenable cyanide. While complexed
cyanide are substantially less toxic, a
review of literature indicates that
significant transformation! of complexed
cyanides into amenable cyanides will
occur in the aquatic environment due to
the presence of sunlight If any water
quality problems occur due to the use of
this alternative, the control authority
should examine alternative
technologies, i.a.. precipitation with
ferrous sulfate.
12. Comment: Several commenters
suggested that fluoride, iron, and
hexavalent chromium be regulated.
Response! The Agency did not
establish limitations for fluorides, iron.
or hexavalent chromium because it was
determined that these parameters were
(1) not present in sufficiently high
quantities to warrant regulation or (2)
would be removed by controlling a
regulated parameter.
The historical performance data for
flouride in effluent from plants with
Option 1 treatment systems shows that
the mean concentration was 8.53 mg/1:
well below levels required by
categorical regulations-for other
industries. i.e.. Inorganic chemicals, and
electrical and electronic components
(phase U.
Iran was not-selected for regulation
because it would be substantially
reduced during proper precipitation/
clarification treatment Thus control of
regulated pollutants will also effect
control of iron.
A limit was not established for
hexavalent chromium because it will be
controlled by regulating total chromium.
The technology basis does include the
cost for hexavalent chromium stream
segregation and reduction. As stated in
the development document chemical
hexavalent chromium reduction can
readily achieve final hexavalent
chromium concentrations of 0.18 mg/1
for a daily maximum and 0.10 mg/1 for a
maximum monthly average.
Additionally, monitoring for total
400
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Federal Register / Vol. 48. No. 137 / Friday. July IS. 1983 / Rules and Regulations
chromium has a distinct cost advantage
over monitoring for hexavaient and
subsequently tnvalent chromium. IX any
of these or other parameters cause
problems with achieving local water
quality requirements, than the control
authority must specify further
requirement* an a piant-by-plant basis.
13. Comment; Several commenters
stated that EPA's method for
distributing costs for indirect
dischargers between the Part 413
electroplating and the Part 433 metal
finishing regulations is misleading and
unrealistic. Electroplating comptianca
costs for captive indirect dischargers
have not yet been incurred. When ties*
plants do comply, it will be with both
regulations in a one-time investment.
Therefore, no costs should be attributed
to Electroplating; rather, all costs should
be considered as Metal Finishing
compliance costs.
Response: The fact that a company
may make a one time investment doesn't
necessarily mean that all the costs
should be attributed to the Part 433.
Metal Finishing Standard. The
compliance date for Part 433 is now
generally two yean after compliance
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Fadaral Register / Vol. «. No. 137 / Friday, July 15. 1S83 / Ruies and Regulations
32481
economic impacts to comply -with Metal
Finishing Guidelines.
Response: The commenters are
correct. The agency has sines analyzed
the impact on indirect discharging
captives with metal Blushing process
flows of less than 10.000 gpd. The
analysis concluded that a total of 312
plants will incur compliance costs. The
total capital cost of compliance for tais
universe is estimated at-S35 million with
annual costs -of S12 million. No closures
or employment effects an protected for
this industry segment
18. Comment: Caranenters questioned
the assumption that the metal finishing
demand curve is inelastic.
Response; Metal finished, products
_ face a wide range of demand
elasticities. However, there are no good
substitutes for metal finishing due to the
quality it imparts on materials. As a .
result, an increase in the cost of metal
finishing will not bring a more than
proportional decrease in the use of
metal finishing. The analysis assumed
that demand for metal finishing is in the
meiasac range but did not assume that
all cost increases could be passed -
through. In fact the captive closure
analysis assumes that a plant's captive
operations will not be able to pass
through a pollution contra! cost increase
if It amounts to more than S percent of
their total revenue. If the ratio of annual
cosls to total revenue was larger than S
percent the plant was projected to
ciose.
19. Comment: Commenters stated that
they thought captive facilities will be al
a competitive disadvantage because job
shops are exempted from metal finishing
standards.
Response: Captives are very rarely in
direct competition with job shops, vying
for the same customers. Captive platers.
by definition, service their own firm's
needs. A captive firm will maintain a
plating process for its cost advantages.
scheduling control and specialty
processes. In the Agency's survey at -
captive facilities, aver 64 percent
indicated they performed metal finishing
m-house because it was either less
expensive to do so or the work flow
didn't allow interruption of work. It 15
true that job shops will ofterf'receive a
caotive's overflow work, but this doe*
not make them price competitors. Also.
almost three-fourths of the indirect
discharging captive facilities and all
direct discharging captives and job
shops already have treatment in place.
To the extent there may be changes in
the competitive position of captives
versus job shops, most of these changes
would have occurred already. Finally.
indirect discharging job shops were
exempted from the metal finishing
regulation specifically because of their
economic vulnerability. Job shops tend
to be much smaller than captives; they
average 26 employees and SL2 million in
sales versus over 100 employees, and 314
million in sales for captives.
20. Commenc A comment was made
that the definition of a job shop may
force some "job shops" to be classified
as captives.
Response £PA proposed a definition
of job shops based on 50% ownership of
treated matanat This is in accord with
existing practice by an overwhelming
portion of th« affected industry. An
examination of the survey of job shops
revealed thaf9S% of th« facilities stated
that their work was either 100% job
ordered or 100% captive. Only OJ8% of
the facilities reported that more than
25%. but less than 50%. of their
production-was dona an materials
owned by others.
The final definition of a job shop has
been modified slightly, makiag.the
measurement of "not more than 50%
ownership" on a yearly basis. This
responds to a umuuemeis' f«ar of
repeated reclassification as a resultof
business transactions. Now facilities
will not be redaswfied on a day-to-day
basis.
The definition is also appropriate
because, the fad that a facility is
purchasing materials to be processed
indicates some availability of capital. If
so the less stringent Part 413 ,
requirements are less appropriate for
The agency considered various job
shop definitions from commantors and
trade association by-laws, including:
" "As its major operation the
application of a surface'treatment to die
products of others."
• "A shop which has purchased
orders from more than SO percent of the
materials in process."
• "Parts to be Smshed are transported
from the customer's plant to the
finishers and then back."
• "As its major operation the
application of a surface treatment to the
products T>f others."
• "A metal finisher who works to
other's specifications, making his
services, available to the public at all
times."
While some of these, notably the first
are close to the proposed and final
definitions, all suggestions included
substantial ambiguity. In light of the
relaxed standards for job shops it is
important that the definition be precise
and that captive shops not evade Part
433 merely by taking on nominal outside
orders. EPA therefore chose a bright-line
test that clearly expressed the
overwhelmingly prevailing practice in
the industry.
EPA's definition is consistent with our
1978 survey of the industry, which asked
for the "percent of electroplating done
on materials owned by others (basis
area plated)" and further defined a |ob
shop as "a manufacturing operation
performing work on materials owned by
others."
XX Availability of Technical
information
The basis for this regulation is
detailed in four major documents-
Analytical methods are discussed in
Sampling cad Analysis Procedures for
Screening of Industrial Sffluanta for
Priority Pollutants. EPA's technical
coociusioas are detailed in Development
Document for Effluent Guidelines, New
Soaree Performance Standards and
Prstreattnent Standards for the Metal
Finishing Point Source Category. The
Agency's economic analysis is
presented in Economic laipaet Analysis
of Effluent Unutaeiom and Standards
for the Metal Finishing industry. A
summary al the public comments
received on the proposed regulation is
presented in a report 'Responses to
Public Comments, Proposed Metal
Finishing Effluent Guidelines and
Standards," which, is part of the public
record for this regulation.
Technical information may be
obtained by writing to Richard Kinca.
Effluent Guidelines Division (WH-552)
EPA. 401 M Street S.W.. Washington.
D.C. 20480 or by calling (202) 382-71S9.
Additional information concerning the
economic impact analysis may be
obtained from Ms. Kathleen
Ehrenaberger. Economics Branch fWH-
588). EPA. 401 M Street S.W.
Washington. D.C 20460 or by calling
(202) 382-6307.
Copies of the technical and economic
documents will be available from the
National Technical Information Service.
Springfield. Virginia 22181. (703) 487-
4650.
XXL OMB R*TWW ,
This regulation was submitted to the
Office of Management and Budget for
review, as required by Executive Order
12291.. No written comments were
received.
In accordance with the Paperwork
Reduction Act of I960 (Pub. L 96-511).
the reporting and recordkeeping
provisions in 40 CFR 413.03 and 433.12
that are included in this regulation will
be submitted for approval to OMB. They
are not effective until OMB approval has
been obtained and the public is notified
402
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32482 Federal Register / Voi. 48. No. 137 / Friday, July 15. 1983 / Ruies and Regulations
to that effect through a technical
amendment to this regulation.
XXH. LUt of subjects
40 CFR Part 413
Electroplating. Metals. Water
pollution control. Waste treatment and
disposal.
40 CFR Part 433
Electroplating. Metals. Water
pollution control. Waste-treatment and
disposal. -
Dated: July 5.1983.
William 0. Rudnfetuu*.
Administrator.
Authority: Sees. 301. 304, 306. 307. 308. and
301 of the Clean Water Act (the Federal
Water Pollution Control Act Amendments of
1373. 33 U.S.C. 1231 at. saq.. 39 amended by
the Claan Water Act of 1977-. Pub. L 95-217;.
(Note.—These appendices will not appear
in the CFH.|
XXIU. Appendices
Appendix A—Abbreviations, Acronyms,
and Other Terms Used in This Notice
Act—The Clean Water Act.
Agency—The U.S. Environmental
Protection: Agency.
SAT—The best available technology
economically achievable under Section
304(b)(2)"(B)oftheAct
SCT—The best conventional pollutant
control technology, under Section
304(b)(4)of the Act
BMPS—Beat management practices
under Section 304(e) of the Act.
BPT—The best practicable control
technology currently available under
Section 304fb)(l) of the Act
Captive—A facility which owns more
than 50% (annual area basis) of the
materials undergoing metal finishing.
Clean Water Act (also "the Act"]—
The Federal Water Pollution Control Act
Amendments of 1972 (33 U.S.C 1251 at
seq.), as amended by the Clean Water
Act of 1377 (Pub. L 9S-217).
Development Document—
Development Document for Effluent
Limitations, CuideJines. and Standards
for the Metal Finishing Point Source
Category, EPA 440-1-SO-091-A. June
1980.
Direct discharger—A facility that
discharges or may discharge pollutants
into waters of the United States.
Indirect discharger—A facility that
discharges or may discharge pollutants
into a publicly owned treatment works.
Job Shop—A facility which owns not
more than 50% (annual area basis) of the
-materials undergoing metal Snishing.
Integrated facility—One that performs
electroplating operations (including
electroplating, eiectroless plating,
chemical etching and milling, anodizing,
coating, and printed circuit board
manufacturing] as only one of several
operations necessary for manufacture of
a product at a single physical location.
and has significant quantities of process
wastewater from non-electroplating
operations. In addition, to qualify as
"integrated." a facility must combine
one or more plant electroplating process
wastewater lines before or at the point
of treatment (or proposed treatment)
with one or more plant sewers carrying
process wastewater from non-
eiectroplating manufacturing operations.
NPDES Permit—A National Pollutant
Discharge Elimination System permit
issued under Section 402 of the Act
NSPS—New source performance
standards promulgated under Section
306 of the Act
POTW—Publicly owned treatment
works.
PSES—Pretreatment standards for
existing sources of indirect discharges
promulgated under Section 307(b) of the
Act.
PSNS—Pretreatment standards for
new sources of direct discharges.
promulgated under Section 307 (b) and
(c) of the Act
RCRA—Resource Conservation and
Recovery Act (Pub. L 9*-380) of 1978.
Amendments to Solid Waste Disposal
Act. as amended.
TTO—Total Toxic Organic* is the
summation of all values greater than .01
milligrams per liter for each of the
specified toxic organics.
Appendix B—Pollutants Excluded From
Regulation
(1) Toxic Pollutants—found in only a
small number of sources and effectively
controlled by the technologies on which
the limits are based:
Antimony
Arsenic
Astaeatoa
Beryllium
Mercury
Selenium
Thallium
(2J Conventional Pollutants:
BOB
Kecal Coliforra
Appendix C—Unit Operations in tin
Metal Finishing Industry
1. ©Electroplating
2. Electroless Plating
3. Anodizing
4. Coating (Chromating, Phosphating,
and Coloring)
5. Chemical Etching and Milling
3. Printed Circuit Board Manufacturing
?. Cleaning
3..Machining
9. Grinding
10. Polishing -
11. Tumbling
12. Burnishing
13. Impact Deformation
14. Pressure Deformation
15. Shearing
18. Heat Treating
17. Thermal Cutting
18. Welding
19. Brazing-
20. Soldering
21. Flame Spraying
22. Sand Blasting
23. Other Abrasive let Machining
24. Electric Discharge Machining
25. Electrochemical Machining
28.. Electron Beam Machining
27. Laser Beam Machining
28. Plasma Arc Machining
29. Ultrasonic Machining
30. Sintering
31. Laminating
32. Hot Dip Coating
33T Sputtering
34. Vapor Plating
35. Thermal Infusion
36. Salt Bath Descaling
37. Solvent Decreasing
38. Paint Stripping
39. Painting
40. Electrostatic Painting
41. Electropainting
42. Vacuum Metalizmg
43. Assembly
44. Calibration
45. Testing
4ft Mechanical Plating
PART 413—€LECTROPLATING POINT
SOURCE CATEGORY
For the reasons stated above. EPA is
amending Part 413~of 40 CFR, Chapter I
as follows:
1. Section 413.01 is amended by
revising paragraph (a) to read as
fallows:
J 41101 AppflaMHiy and compriamce
(a) This part shall apply to
electroplating operations in which metal
is electroplated on any basis material
and to related metal finishing operations
as set forth m the various subparts.
whether such operations are conducted
in conjunction with electroplating,
independently, or as part of some other
operation. The compliance deadline for
metals and cyanide at integrated
facilities shall be June 30.1984. The
compliance date for metals and cyanide
at non-integrated facilities shall be April
27,1984. Compliance with TTO for all
facilities shall be July 15.1988.' These -
1 The Consent Q«m in MRDC v. Train. 12 SRC
1833 (D.D.C. 1979) specifies a compliance date for
PSES of no later than iune 20.1964. EPA has moved
for a modification of that provision of the Decree.
Should the Court deny that motion. EPA will be
required to modify this compliance date~—
accordingly.
403
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Federal Register / Vol. 48. No. 137 [ Friday. July 15. 1983 / Rules and Regulations 32483
Part 413 standards snail not apply to a
facility which must comply with aJl the
pollutant limitations listed in f 433.15
(metal finishing PSES).
2. Section 413.02 is amended by
adding a new paragraph (i). aa follows
§413.02
(i) toe terra TTO" shall mean total
toxic organics. which is the summation
of all quantifiable values greater than
0.01 milligrams per [iter for the following
toxic orgarucs:
Acniein
AcryJonitnle
Benzane
Bsnzidine
Carbon tetrachiontjts
(tetrachloroinethane)
C&torobeazaa*
t.2.4-
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Federal Register / Vol. '48. No. 137 / Friday, fuly 15. 1983 / Rules and Regulations
submitting a certification in lieu of
monitoring pursuant to I 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
5. Secton 413.24 is amended by adding
paragraph (f), (gj and (h). as follows:
341124 prxrattMnt standard* for
(f) la addition to paragraphs (a) and
(b) the following limitation snail apply
for plants discharging leas than 38.0001
(10.000 gal] per calendar day of
electroplating process wastewaten
(g} In- addition to paragraphs (a|, (c),
(d), and (a) the following limitation shall
apply for plants discharging 38.0001
(10.000 gal] or more per calendar day of
electroplating process wastewatan
MM Mr
an \
(h) In addition to paragraphs (a), (b).
(c), (d). (e), (f), and (3) the following
shall apply: An existing- source
submitting a certification in lieu of
monitoring pursuant to \ 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
a. Section 413.44 is amended by -
adding paragraph (f), (gj. and (h), as
follows:
141X44 PrvftMttnntstmteni* to-
ff) In addition to paragraphs (a) and
(b) the-following limitation shall apply
for plants discharging lets than 38.0001
[10.000 gai) per calendar, day of
electroplating process wastewaten
mum lor
any I
aw
[g) In addition to paragraphs (afc (c),
(d). and (e) the following limitation shall
apply for plants discharging 38.0001
(10.000 gal) or more per calendar day of
electroplating process wastewater:
(b) In addition to paragraphs (a), (b),
(c). (d), (eUO. and (gj the following
shall apply: An existing source
submitting a certification in lieu of
monitoring pursuant to \ 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
7. Section 413.54 is amended by
adding paragraph (f), (g), and (hi. as.
follows:
I (or
(f) In addition to paragraphs (a) and
(bj the following limitation shall apply
for plants discharging leas than 38.0001
(10.000 gal] per calendar day of •
electroplating process wastewaten
(g) In addition to paragraphs (a), (c),
(d). and (e) the following limitation shall
apply for plants discharging 38.0001
(10,000 gal) or more per calendar day of
' electroplating process waterwaten
(h) In addition to paragraphs (a), (b),
(c}. (d), (e). (f), and (g> the following
shall apply: An existing source
submitting a certification in lieu of
monitoring pursuant to 5 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
a. Section 413.94 is amended by
adding paragraphs (f), (g), and (h), as
follows:
§413.64 Pl«UMUii«
Mentetor
(f) In addition to paragraphs (a) and
(b) the following limitation-shall apply
for plants discharging less than 33.0001
(10.000 gal) per calendar day of
electroplating process wastewater
mum tor
! ** i
i a*
(gj In addition to paragraphs fa), (c),
(d), and (e) the following limitation shall
apply for plants discharging 39.0001
(10,000 gal) or more per calendar day of
electroplating process wastewaten
(h) In addition to paragraphs (aj, (b|.
(cj, (dK(e), (f), and (g) the following
shall apply: An existing source
submitting'a certification in lieu of
monitoring pursuant to I 413.03 of this
regulation must implement the toxic
organic management plan approved by
the- control authority.
9. Section 413.74 is amended by
adding paragraphs (f). (gj and (h). as
follows:
§4117*
ototfngs
(f) In addition to paragraphs (a) and
(b) the following limitation shall apply
foe plants discharging less than 38.0001
(10.000 gal) per calendar day of
electroplating process wastewater-
is) In addition to paragraphs (a), (c),
(d). and (e) the following limitation shall
apply for plants discharging 38.0001
(liooffgai] or more per calendar day of
electroplating process wastewaterr
no
(h) In addition to paragraphs (a), (b),
(c), (d). (e|. (f). and (g) the following
shall apply: An existing source
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Federal Register / Vol. 48, No. 137 / Friday. July IS. 1983 / Rulas and Regulations
32485
submitting a certification in lieu of
monitoring pursuant to § 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
10. Section 413.84 is amended by
adding paragraphs (f). (g) and (h). as
follows:
§ 41X84 PfWMUmnt standard* for
(!) In addition to paragraphs (a) and
(bj the following limitation shall apply
for plants discharging less than .38.000 1
(10.000 gal) per calendar day of
electroplating process waste water
(g) In addition to paragraphs (a), (c),
(d), and (e) the following limitation shall
apply for plants discharging 38.0001
(10.000 gal) or more per calendar day of
electroplating process wastewater:
Pqdunm or MMMNK orapvny
TO.....
fh| In addition to paragraphs (a), (b),
(c). (d). (e). in. and (g) the following
shall apply: An existing source
submitting a certification in lieu of
monitoring pursuant to § 413.03 of this
regulation must implement the toxic
organic management plan approved by
the control authority.
In addition, for the reasons stated
above. EPA is establishing a new Part
433 to Title 40 of the Code of Federal
Regulations to read as follows;
PART 433— METAL FINISHING POINT
SOURCE CATEGORY
Flo
fHng Su
eqory
S«c.
433.10 Applicability: description of the maul
finishing point source category.
433.11 Specialized definitions,
433.12 Monitonng requirements.
433.13 Effluent limitations representing the
degree of effluent reduction attainable by
applying the best practicable control
technology currently available (BPT).
433.14 -effluent limitations representing the
degree of effluent reduction attainable by
applying the best available teohnoiogy
economically achievable (BAT).
433.13 Pmreatment standards for existing
sources (PSES).
433.18 New source performance standards
(NSPS).
433.17 Ptetreatment standards for new
sources (PSNS).
433.13 (Reserved)
Authority: Sec. 301. 304(b). (c). (e). and (g).
308(b| and (e). 3O7(b) and (c). 308 and SOI of
the Clean Water Act (the federal Water
Pollution Control Act Amendments of 1971.
as amended by the Clean Water Act of 1977)
(the "Act"]; 33 U.S.C. 1311.1314(b| (c), (e).
and (g). 1316(b) tod (c|. !317(bl and (c). 1318
and 1361: M Slat 818. Pub. L. 92-500:91 Stat
1567, pub. L.99-a7.
Subpart A—M«tal Finis
Sutwatagery
§433.10 AppffcaMHty;
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32486
Federal Register / Vol. 48. No. 137 / Friday, July 15, 1983 / Rules and Regulations
Benzo(a]pyrene (3.4-benzopyrene|
3.4-3enzot1uoranthene I benzoib | fluoranthene I
11.12-benzotluoramhene
(benza(k)fluorantheiw)
Chrysene
Acenaphthylane
.Anthracene
1.12-benzoperyien»(benzo(ghi)perylene|
Fluorane
Phenanthrene
1.2.5.8Kiibenzamhracene-
(dibeH2o(a.h)anthracene
Indeno(l.i3-cd) pyrene (2.3-o-phenlene
pyrene)
Pyrene
Tetrachloroethytene .
Toiiwne
Tnchloroethyleiu
Vinyl chlonde (chloroethyiana)
3.3-dichlorobenzidiiie
1.1-dichloroethyiena
l,2-ffai»dichloroethylen«
2.4-dichloraphenai
1.2- bant practlcaPta control
tecnnoteBD cummiyanrilaM* (BPT).
(a) Except as provided in 40 CFR
125.30-32. any existing point source
subject to this subpart must achieve the
following effluent limitations •
representing the degree of effluent
reduction attainable by applying the
best practicable control technology
currently available (HPT):
SPT &RUSNT LIMITATIONS
Cooo«r ("0 LLU. .......
sine rn
TTT}
T53 _
! 0.8> i
- i 3TT |
i 138 1
1 TW '
1 Q^3 1
„_. j 2.81
,„ „„ I i 20 1
.. ._! 113 ;. ...
..1 ffl
107
043
i:a
02«
1 48
ass
:i
i1)
' wmn wai.0,
(b) Aitemativeiy, for mdustnai
faculties with cyanide treatment ard
upon agreement between a source
subject to those Hmits and the pollution
control authonty. the following
amenable cyanide limit may apply '.n
place of the total cyanide limit specified
m paragraph (a) of this section:
, Mommy
for i av«raq«
o
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Faderal Register / Vol. 48. No. 137 / Friday. July IS. 1983 / Rules and Regulations 32487
BAT Si=RU6NT LIMITATIONS—Conanuad paragraph (a) of this section:
(b) Alternatively, for industrial
facilities with cyanide treatment and
upon agreement between a source
subject to those limits and the pollution
control authority, the following
amenable cyanide limit may apply in
piace of the total cyanide limit specified
in paragraph (a) of this section:
(c) No user subject to the provisions of
this subpart shall augment the use of
-process wastewater or otherwise dilute
the wastewater as a partial or total
substitute for adequate treatment to
achmve compliance with this limitation.
5*33.15 PratrwmMnt stmoanto for
nutting soure** (PSES),
(a) Except as provided in 40 CFR 403.7
and 403.13. any existing source subject
to this subpart that introduces pollutants
into a publicly owned treatment works
must comply with 40 CFR Part 403 and
achieve the following pretreatmant
standards for existing sources (PSES):
(c) No user introducing wastewater
pollutants into a publicly owned .
treatment works under the provisions of
this subpart shall augment the use of
process wastewater as a partial or total
substitute for adequate treatment to
achieve compliance with'this standard.
(d) An existing source submitting a
certification in lieu of monitoring
pursuant to ! 433.12 (a) and (b) of this
regulation must implement the solvent
management plan approved by the
control authority.
(e) An existing source subject to this
subpart shall comply with a daily
maximum pretnatment standard for
TTOof4J7mg/L
(f) Compliance with the provision* of
paragraph (c). (d), and (e) of this section
shall be achieved as soon as possible.
but not later than June 30.1984. however
metal finishing facilities which are also
covered by Part 420 (iron and steel]
need not comply before July to, 1966.'
Compliance with the provisions of
paragraphs (a), (b), (c] and (d) of this
section shall be achieved as soon as
possible, but not later than Feburary 15.
1980.'
5433.1* H«w aoure* tMrtommta*
FOR Au, PUWTS EXCEPT JOB SHOPS
»NO INOEKNOeNT PRINTED CWCUT BOAflO
MANUFACTURERS
(a) Any new source subject to this
subpart must achieve the following
performance standards;
NSPS
(b) Alternatively, for industrial
facilities with cyanide treatment upon
agreement between a source subject to
those limits and the pollution control
authority. The following amenable
cyanide limit may apply in place of the
total cyanide limit specified in
MMs 10 n 9.0,
' Tha CoOMnt Doene in NRDC v. Tram. 12 ERC
1833 [O.O.C, 19791 speaflM a comptiancB da« for
PSES of no lanr than June 30. 1964. EPA has oi
for a modification of (hat provision at th« Oacrm.
Should th« Court dany.thal motion. ^A wtit br
required to modify tht* compliance date
accordingly
(b) Alternatively, for industrial'
facilities with cyanide treatment and
upon agreement between a source
subject to those limits and the pollution
control authority, the following
amenable cyanide limit may apply in
place of the total cyanide limit specified
in paragraph (a) of this section:
(c) No user subject to the provisions of
this subpare shall augment the use of
process wastewater or otherwise dilute
the wastwater as a partial at total
substitute for adequate treatment to
achieve compliance with this limitation.
5 433.17 Pieti'MUmm lUrxUnM for new
(a) Except as provided in 40 CFR
403.7, any new source subject to this
subpart that introduces pollutants into a
publicly owned treatment works must
comply with 40 CFR Part 403 and
achieve the following pretreatment
standards for new sources (PSNS):
PSNS
sfc«
-------
32488- Federal Register / Vol. 48, No. 137 / Friday. July 15. 1983 C Rules and Regulations
(c) No user subject to the provisions of
this subpart shall augment the use at
process wastewater or otherwise dilute
the wastewater as a partial or total
substitute for adequate treatment to
achieve compiiance-with this ITmUation.
[dl An existing source submitting a
certification in lieu of monitoring
pursuant to $ 433.12 (a) and (bj of this
regulation must implement- the solvent
management plan approved by the
control authority.
[FH OOC.
-------
APPENDIX C
METRIC-ENGLISH UNITS CONVERSION
English
1 horsepower (HP)
1 gallon
1 gallon
1 ft
1 ft2
1 ft3
1 GPD/ft2
1 Ib/gallon
1 ft/sec
1 Ib
Metric
745.7 Watts
0.0037854 m3
3.7854 L
0.3048 m
0.0929 m2
0.0283 m3
0.0407 m3/day/m2
1 .20 x 105 mg/L
18.288 m/min
453.59 g.
410
-------