------- ENVIRONMENTAL PROTECTION AGENCY TR-1 WATER QUALITY OFFICE TOTAL ORGANIC CARBON REMOVAL FROM MUNICIPAL AND INDUSTRIAL WASTEWATER by James L. Hatheway Division of Field Investigations - Denver Center Denver, Colorado 80225 March 1971 ------- TOTAL ORGANIC CA1I( R IOVAL FROM MUNICIPAL AND INDUS1 1AL WASTEWATER Abstract Physical-chemical treatment processes provide overall removal of organic waste matter of more than 95 percent on raw domestic or domestic-industrial wastewaters desptte variations in organic loadings and the presence of toxic chemicals. The annual operating cost for physical-chemical treatment of raw wastewaters is equal to or less than the cost of conventional biological treatment. i ------- TABLE OF CONTENTS Title LIST OF TABLES INTRODUCTION SU O1ARY REVIEW OF LITERAflJRE. ACTIVATED CARBON COSTS ADSORBENT RESINS OXIDATION PROCESSES.. BIBLIOGRAPHY Page 111 1 3 4 4 14 16 21 22 11 ------- LIST OF TABLES No. Title Page 1 ROCKY RIVER WASTE TREATMENT PLANT CLARIFICATION/CARBON 5 PROCESS 2 TREATMENT OF PRIMARY EFFLUENT BY POWDERED CARBON, 5 LEBANON, OHIO 3 TREATMENT OF PRIMARY EFFLUENT BY GRANULAR CARBON, 8 LEBANON, OHIO 4 TOC REMOVAL 9 5 BOD REMOVAL 10 6 TREATMENT OF SECONDARY EFFLUENT BY FILTRATION, CHEMICAL 11 CLARIFICATION AND/OR CARBON ADSORPTION 7 CARBON ADSORPTION PILOT PLANT AVERAGE WATER QUALITY 13 CHARACTERISTICS, JUNE 1965 TO JULY 1969 8 INDUSTRIAL WASTE ADSORPTION TREATMENT PLANTS 15 9 CAPITAL AND OPERATING COSTS, GRANULAR CARBON ADSORPTION. . . 17 10 CAPITAL COST COMPARISON 18 11 OPERATING AND MAINTENANCE COST COMPARISON 19 12 TOTAL COST COMPARISON 20 111 ------- INTRODUCTION This paper summarizes the results of studies undertaken to deter- mine methods of removing total organic carbon (TOC) from municipal and industrial wastewaters. A conventional biological treatment facility will provide, at best, approximately 90 percent removal of suspended solids and biochemical oxygen demand (BOD). Although the effluent from these plants meets current state water quality regulations, more stringent demands are being instigated to remove a greater amount of the contaminants, such as phosphate, nitrate and total organic carbon, from wastewater before it is discharged into the receiving waters. Two possibilities are available to remove organic contaminants from wastewater. These are to provide tertiary treatment to the effluent from the secondary biological treatment facility, thereby significantly increasing the cost of treatment, or to provide treatment of raw wastewater by a physical-chemical treatment process. The physi- cal-chemical process includes chemical clarification, filtration, and adsorption Granular activated carbon adsorption has proven to be one of the most successful and economical advanced waste treatment processes and is in full-scale operation in municipal water, municipal wastewater and industrial wastewater treatment facilities (2) (3) (4) (5) (6). When used in conjunction with chemical precipitation and filtration, 95 percent or greater removal of TOC, BOD, chemical oxygen demand (COD), total phosphates and suspended solids and 78 percent of total nitrogen - Numbers in parentheses refer to bibliography. ------- 2 can be removed from raw wastewater (7). In addition, the carbon ad- sorption process, as a secondary treatment step, has the following potential advantages over biological processes (3). 1. The land requirement can be as much as 10 times greater for a biological treatment facility. 2. The capital costs are higher for a conventional biological process. 3. Shock loadings, toxic wastes and low temperatures have less effect on carbon adsorption. 4. Operating conditions can be easily changed in a carbon adsorption system to meet varying influent quality flow changes. 5. Odor problems are reduced with the carbon adsorption process. 6. The volume of sludge produced is greater in a conventional biological process. ------- 3 SUMMARY A review of literature shows that efficient removal of TOC from secondary effluents and raw wastewater, either domestic or domestic- industrial in origin, is practicable. Physical-chemical treatment facilities, consisting of chemical clarification, filtration and carbon adsorption, can remove more than 95 percent of the TOC from either secondary effluents or raw wastewaters. The physical-chemical treatment process should be applied directly to raw wastewaters, as this provides the best quality effluent at the lowest cost. Studies have shown that for a 10 million gallon per day wastewater flow, the capital and annual operating costs for a physical- chemical facility are less than for an activated sludge facility. Es- timates of annual operating cost for physical-chemical treatment vary from $0.03 to $0.11 per 1,000 gallons of wastewater treated, depending on size and design efficiency of the treatment facility. Although there has been only a small number of studies conducted on removal of organic contaminants from industrial wastewaters, the physical-chemical treatment process should provide an excellent quality effluent, as this process is not affected by shock loadings, pH fluctu- ations, changes in temperature or toxic substances. ------- 4 REVIEW OF LITERATURE processes for increased removal of organics from domestic and industrial wastewater streams are in varying stages of development. These processes include: 1. Activated Carbon 2. Adsorbent Resins 3. Oxidation Processes ACTIVATED CARBON Over the last few years, many lab and field evaluation tests have confirmed the technical and economic feasibility of treating raw waste- water and secondary effluent with activated carbon to remove organics. This •has resulted in the application of a physical-chemical process to treat wastewater. This process utilizes: (a) chemical clarification, either lime precipitation or metallic salts (FeC1 3 or alum), and filtra- tion to remove colloidal substances, and (b) adsorption of organics by activated carbon (1) (7). The following paragraphs summarize either completed or on-going work utilizing carbon adsorption practices. A granular activated carbon wastewater treatment process has been demonstrated at the Cuyahoga County wastewater treatment facility in Rocky River, Ohio (3). This carbon adsorption process treated chemically clarified raw sewage and produced an effluent which was better than effluents normally obtained from conventional biological secondary treatment facilities. Data from the Rocky River study are summarized in Table 1 (8). The clarification/adsorption process removed 75 percent of the TOC, 81 percent of the COD and 93 percent of the BOD contained in the raw sewage. ------- 5 TABLE 1 ROCKY RIVER WASTE TREATMENT PLANT CLARIFICATION/CARBON PROCESS! ’ Carbon Column Effluent Raw Clarified Carbon Contact Time, Minutes Percent Water Water 4.7 14 23.4 32.6 Removed Suspended 107 65 31 13 15 7 93.3 Solids mg/i BOD, mg/i 118 .57 27 21 ii 8 93.3 COD, mg/i 235 177 117 67 50 44 81.3 TOC, mg/i 52. 53 33 18 15 13 75 1/ Data from Rizzo, J. L., and R. E. Schade, “Secondary Treatment with Granular Activated Carbon.” Water and Sewage Works, August 1969. (8) TABLE 2. TREATMENT OF PRIMARY EFFLUENT BY POWDERED CARBON, LEBANON, OHIO J TOC Powde red . Run Carbon (mg/I) Flow (gptn) Primary Effluent (mg/i) Carbon Effluent (mg/i) Percent Removal 3 200 5 69.0 10.2 85.2 5 200 5 41.7 3.7 91.1 6 200 5 46.3 4.1 91.1 7 200 5 48.4 6.7 86.1 9 300 5 67.1 11.0 83.6 1/ Data from Masse, Arthur N., “Removal of Organics by Activated Carbon.” Robert A. Taft Water Research Laboratory, August 1968 (Tnimeo) (3). ------- 6 A 7200 gallon per day physical—chemical pilot plant was field tested for one year at the Ewing-Lawrence Sewage Authority wastewater treatment facility near Trenton, New Jersey. The wastewater is comprised of approximately 25 percent industrial wastes and 75 percent domestic wastes (1). This pilot plant consistently provided greater than 95 percent removal of TOC and BOD despite the variations in waste strengths and composition. The effluent contained 0.5 milligrams per liter (mg/l) or less of TOC compared to about 30 mg/I for the same wastewater treated conventionally by a trickling filter. The phosphate and nitrate removal rate was 90 percent or greater during the study. In addition, the study showed that 340 lbs. of activated carbon will remove approximately 45 lbs. of TOC (1). The 10 gallon per minute powdered activated carbon pilot plant at Lebanon, Ohio, waste treatment facility operates on primary effluent (3). TOC removal varied from 83 to 91 percent and is summarized in Table 2. The final effluent from this carbon adsorption process was always less turbid and lower in organic carbon than the effluent produced by the activated sludge plant operating on the same primary-treated wastewater (3). Activated sludge normally does not reduce the organic carbon concentra- tion below 20 mg/l (9). The Lebanon facility has also been tested using granular activated carbon (10). The lime clarification-carbon adsorption system operates at steady flow conditions treating primary effluent. This primary effluent is fed to the lime clarification process for removal of sus- pended matter and phosphates. The wastewater then passes through dual- media filters to the carbon contactors for removal of additional soluble ------- 7 organics. The clarification process by itself removed 76 percent of the TOC. The overall removal of ROD, TOC, and COD by this process was 87 percent. Table 3 summarizes the organic removal from the system. The authors (10) suggest that the TOC removal rate may be lower than what could be expected since the carbon columns were not designed for efficient backwashing. This inability to efficiently backwash the carbon columns could reduce the amount of activated carbon available for organic adsorption. Physical-chemical treatment of the District of Columbia raw waste- water in a 100,000 gpd pilot plant which consists of two-stage lime pre- cipitation, filtration, pH control, ion exchange and carbon adsorption provided 98 percent, 95 percent, and 78 percent removal of phosphorus, organics and total nitrogen, respectively, for the 6-month operating period (7). The lime treatment phase of this process alone removed approximately 96 percent of the phosphorus and 80 percent of the BUD, TOC and COD. The final effluent from the carbon adsorption beds con- tained average residual organics of 5 mg/ i BOB, 6 mg/l TOC and 13 mg/i COD. Tables 4 and 5 summarize the removal rates of TOC and BUD in each step of this physical-chemical process.. Personnel of the Robert A. Taft Sanitary Engineering Cent er con- ducted pilot-scale studies of adsorption on granular carbon from four dif- ferent secondary effluents derived from domestic and industrial wastes (2). These waste sources had been treated by either activated sludge or trickling filters. The study determined removal of TOC, turbidity and phosphate from these secondary effluents by either filtration and carbon adsorption or chemical clarification, filtration and carbon adsorption. Table 6 ------- 8 TABLE 3 TREATMENT OF PRIMARY EFFLUENT BY GRANIJLAR CARBON 1/ LEBANON, OHIO BOD TOC COD SS P Turbidity (mg/i) (mg/i) (mg/i) (mg/i) (mg/i) (JTU) Primary Effluent 76 76 192 85 9 55 Lime Clarification and 25 2 6 67 10 1 2. Dual Media Filtration Effluent Granular Carbon 10 11 27 1 1 1 Effluent Overall Removal (%) 86.8 85.5 86.9 98.7 88.9 98.2 Average ratios determined from study BOD 10 COD TOC — . 8 TOC 3.13 if Data from Villiers, R. V., E. L. Berg, C. A. Brunner, and A. N. Masse, “Treatment of Primary Effluent by Lime Clarification and Granular Carbon.” Advanced Waste Treatment Research Laboratory, Nay 1970. (10) ------- TABLE 4 TOC REMOVAL 1 ’ Month (1970) Influent (mg/i) Clarification Residual Percent (mg/i) RemovaLV Filtration Residual Percent (mg/l) Removai. ’ Ion Exchange 1 ! Residual Percent (mg/i) RemovaiF Adsorption Residual Percent (mg/i) RemovalF March 118 2.5.5 78 20.1 83 14.9 87 3.7 97 April 102. 22.8 77 19.9 81 14.8 85 4.9 95 May 114 18.8 84 16.8 85 13.5 88 8.1 93 June 85 18.1 79 18.5. 78 14.5 83 8.3 91 July 78 17.6 78 17.3 78 11.8 82 5.2. 93 August 96 17.5 82 18.4 81 6.1 93 ” 7.6 1/ Data for District of Columbia 100,000 gpd physical-chemical pilot plant. Table from D. F. Bishop, T. P. O’Farrell, and J. B. Stamberg, “Physical-Chemical Treatnient.of Municipal Wastewater.” Robert A. Taft Water Research Center, October 1970 (7). 2/ Intermittent Operation, percent removal based on intermittent influent concentration. 3/ Accumulated percent.removal. 4/ Ion exchange placed after adsorption. ------- TABLE 5 BOD REMOVAL— Month (1970) Influent (mg/l) Clarification Residual Percent (mg/i) RemovalF Filtration Residual Percent ,, (mg/i) Removai ’ Ion Ex Residual (nig/l) change - i Percent 31 Removal—’ Adsorption Residual Percent 3 (mg/l) Removal— March 142 31.4 78 2.3.7 83 16.7 88 3.7 98 April 12.6 2.8.3 78 24.3 81 18.6 85 6.4 95 May 158 2.6.1 83 19.4 88 12.6 90 . 6.5 96 June 111 18.1 84 15.1 86 9.6 90 7.5 93 July 99 13.0 86 11.8 88 7.8 92 3.0 97 August 98 . 16.2 83 13.9 86 4.3 93& 4.7 1/ Data for District of Columbia 100,000 gpd physical-chemical pilot plant. Table from D. F. Bishop, T. P. O’Farrell, and J. B. Stamberg, “Physical-Chemical Treatment of Municipal Wastewater.” Robert A. Taft Water Research Center, October 1970 (7). 2/ Intermittent Operation, percent removal based on intermittent influent concentration. 3/ Accumulated percent removal. 4/ Ion exchange placed after adsorption. . ------- Symbol Source A Batavia - B Lebanon C Hamilton D Remington E “Primary” 2/ Ca lime as CaC; Al alum as A1 2 (S0 4 ) 1 .14H 2 0. 3/ In = input value; Fiit. = after filtration only; Clar. after chemical clarification and filtration; Fiit.-Carbon after filtration and carbon adsorption; Clar.-Carbon = after chemical clarification, filtration and carbon adsorption. 4/ Indicates jar tests; not filtered. 5/ Partially clarified with alum. 6/ 38-minute empty-bed contact time; all others 20-minute bed contact time. 7/ Data from D. F. Bish, L. S. Marshall, T. P. O’Farreil, R. B. Dean, B. O’Connor, R. A. Dobbs, S. H. Criggs, and R. V. Villiera. “Studies on Activated Carbon Treatment.” Journal Water Pollution Control Federation, February 1967 (2). EP.BLE & TREAThENT OF SECONDARY EFFTJJENTS BY FILTRATION, CHEMICAL CLARIFICATION AND/OR CARBON ADSORPTIONZ/ Dose P lantI/ Chem. J (mg/i) In i Turbiditya’ (JTU) TOC .’ (mg/i) Phosphates 3 i (mg/i) Put.— Filt. Carbon Ciar. Clar.- Carbon In Filt.— Ciar.— Put. Carbon Clar. Carbon In Clar. Al Al Al Ca Al Ca Ca Ca Al Ca Al Ca Ca Al Ca Ca A- l - ’ A- 2fü A-3 A-3 A-4 A-5 B- l i B- 2 ’ B-3 1/ 260 400 450 450 300 303 133 151 350 227 300 300 151 150 150 378 19 1.1 0.3 0.7 10 6.7 0.2 15 10 0.5 0.6 0.6 7.1 5.5 0.2 15 8.7 1.6 0.3 120 31 31 21 35 9.5 18 90 200 13 13 14 130 130 120 11 0.6 0.1 0.3 0.2 1.3 0.7 3.3 0.9 0.8 7.0 0.9 33 4 30 1 17 19 9 0 11 0 12 10 8 0 13 0 11 13 9 0 16 18 - 116 14 71 72 72 18 17- 4 24 19 5 15 20 19 14 4 40 18 5 15 15 12 12 2 37 37 189 157 22 Type of Waste Domestic Domestic Mixed Domestic Domestic 58 58 19 23 35 33 21 29 24 24 20 11 ii 0.0 0.0 0.8 1.0 1.0 0.4 0.0 0.5 0.8 2.0 2.8 0.0 0.4 0.2 8.8 - 6.5 39 28 Type of Treatment Trickling Filter Activated Sludge Activated Sludge Trickling Filter Overloaded Trickling Filter ------- 12 shows the removal of turbidity, TOC and phosphate by either filtration; filtration and carbon adsorption; filtration and chemical clarification; or filtration, chemical clarification and carbon adsorption. As can be seen in this table, chemical clarification and filtration alone removes TOC from an influent range of 12-72 mg/i to an effluent range of 8-33 mg/l. When the effluent from this clarification step is passed through the carbon adsorption columns, the TOC is further reduced with the final effluent having 1 mg/I or less of TOC. This suggests that the extent of residual TOC in the original secondary effluent was an unadsorbable frac- tion on the order of I mg/l (2). A 0.3 MCD granular activated carbon pilot plant has continuously treated unfiltered activated sludge effluent from the Pomona water re- clamation plant from June 1965 through July 1969 (11) (12). Successful backwashing of the first stage activated carbon column, which served as a filter and adsorber, made pretreatment of the secondary effluent un- necessary. The average TOC concentrations in the influent and effluent from this pilot plant study were 12 and 3 mg/l respectively (75 percent TOC removal). Table 7 summarizes the average water quality character- istics of this study. Other municipalities which utilize carbon adsorption include Cincinnati, Ohio; Wayne County, Michigan; Cortland, New York; Leetsdale, Pennsylvania; South Tahoe Public Utility District, California; and Nitro, West Virginia (3) (6). Except for Cincinnati, TOC data were not avail- able. Cincinnati removes 86 percent of the TOC in its physical-chemical wastewater facility (6). ------- 13 TABLE 7 CARBON ADSORPTION PILOT PLANT AVERAGE WATER QUALITY CHARACTERISTICS1’ ’,V JUNE 1965 to JULY 1969 PARAMETER INFLUENT EFFLUENT SUSPENDED SOLIDS mg/i 9 0.6 COD mg/i 43 10 DISSOLVED COD mg/i 30 8 TOC mg/i 12 3 NITRATE as N mg/i 8.1 6.6 TURBIDITY (Jtu) 8.2 1.2 COLOR (Platinum-Cobalt) 28 3 ODOR (Ton) 12 1 CCE mg/i 0.026 BOD mg/i 3 1 1/ Data for Pomona, California, Water Reclamation Plant. 2/ Table from 3. N. English, A. N. Masse, C. W. Carry, J. B. Pitkin, and 3. E. Haskins, “Removal of Organics from Wastewater by Activated Carbon.” Advanced Waste Treatment Seminar, San Francisco, California, October 28-29, 1970 (12). ------- 14 Industrial wastewater treatment facilities experience wide fluctu- ations in raw wastewater characteristics. Biological systems operate least effectively under fluctuating temperature and pH conditions, and in addition, dyes, detergents and other refractory contaminants can pass through these systems without receiving any degree of treatment. Toxic wastes upset biological waste treatment facilities. Due to these and other factors, carbon adsorption systems are being utilized by industry (6). Table 8 lists •a variety of industries which presently treat their wastewaters by carbon adsorption techniques. An investigation of the removal of color and organic carbon from a paper mill bleaching effluent was conducted at Continental Can Co., Augusta, Georgia (13). This investigation utilized only the chemical clarification step in the physical-chemical process. Aluminum chloride was found to be the most economical coagulant, removing 80 percent of the color and 30 percent of the total carbon. Costs The major portion of the operating costs for treatment of wastes by activated carbon relates to the amount of carbon exhausted per unit of wastes treated. Based on the pilot plant study, Rocky River, Ohio, will construct a 10 NGD treatment facility at a cost of $1.6 million. This is $200,000 less than the cost of the conventional activated sludge plant designed to treat this same wastewater. The annual operating cost for the adsorption portion of the process is estimated at $0.03/bOO gal. (8). The Pomona Pilot Plant Study results indicate that the cost of a 10 MGD waste treatment facility utilizing carbon adsorption with no pretreatment of the secondary effluent would be $O.08/l,000 gal. of treated wastewater (11). ------- TABLE 8 INDUSTRIAL WASTE ADSORPTION TREATMENT PLANTS 1 ’ REACTI VATION OR AVERAGE REGENERATION LOCATION IMPURITY FLOW RATE METhOD 1. Washington, New Jersey Polyols 100 gpni Furnace 2. E. St. Louis, Illinois Nitropheriol 50 gpni Caustic 3. Burlington, Iowa TNT 100 gpm None 4. Southampton, Pa. Dye 350 gpin Furnace 5. Portland, Oregon Insecticides 100 gpin Furnace 6. Conway, North Carolina Phenol 25 gpm Caustic 7. Wilmington, California Refinery 2,900 gpm Furnace Wastes 8. Latrobe, Pa. Cyanide 20 gpm 1/ Table from D. G. Hager and P. B. Reilly, ‘ t Clarification-adsorption in the Treatment of Municipal and Industrial Wastewater.” Presented at the 42nd Annual Conference of the Water Pollution Control Federation meeting in Dallas, Texas, October 5-10, 1969 (6). ------- 16 Table 9 summarizes capital and operating costs for four plants, three for secondary effluent treatment and one (Rocky River) for primary effluent treatment. These cost estimates were made by different groups and therefore differ in procedure for calculating’such items as overhead, maintenance and amortization. Each plant also differs in process con- figuration and objective’; therefore, care should be taken not to directly compare one with another (3). The economics of a clarification-adsorption process compared to an activated sludge facility for a 10 I D wastewater flow are given in Tables 10, 11 and 12 (6). The primary treatment portion for both the activated sludge facility and the clarification process is identical. The capital cost for a clarification..adsorption process is less than for an activated sludge facility (Table 10). The annual operating costs, on the other hand, are higher for carbon adsorption (Table 11). combining the operating costs with amortization of capital shows that the costs of the two systems are essentially the same for the 90 percent BOD removal level (Table 12). Should a higher degree of treatment be required in the future, the clarification-adsorption system could deliver up to 95 percent BOD removal for an increase of 0.7 cent per 1,000 gal. annual operating cost. The activated sludge facility would require the addition of a “tertiary tt system to achieve the 95 percent BOD removal level, thus resulting in additional capital costs. This would result in a cost much greater than the 0.7 /l,000 gal. required for the carbon adsorption process. ADSORBENT RESINS Adsorbent synthetic resins are being investigated as alternatives ------- TABLE 9 CAPITAL AND OPERATING COSTS 1 ’ GRANULAR CARBON ADSORPTION Pittsburgh Activated Lake Rocky Carbon Co. Tahoe Pomona River Capacity, MCD 10 7.5 10 10 Investment ($1,000) 1,489 1,306 1,670 1,600 Operating Cost (Q/l0 0 0 gal.) Carbon 1.20 1.18 1.10 0.69 Fuel 0.11 ---- 0.25 0.12 Chemicals ---- 0.99 3.80 Power 0.85 0.75 0.85 0.55 Labor 0.74 0.40 1.50 1.10 Overhead 0.27 Amortization 3.07 3.53 4.10 3.23 (20 Years) (20 Years) (15 Years) (20 Years) Maintenance 0.63 0.33 0.50 0.55 Total Operating Cost 6.87 7.18 8.30 10.04 1/ Table from Arthur N. Masse, “Removal of Organics by Activated Carbon.” Robert A. Taft Water Research Laboratory, August 1968 (mimeo) (3). ------- 18 TABLE 10 CAPITAL COST COMPARISON!! 10 MGD Plant In Thousands of Dollars Activated Clarification Primary Sludge Adsorption Preliminary 75 75 75 Preaeration 98 98 98 Primary Settling 275 275 275 Activated Sludge System 730 Secondary Settling 200 Adsorption 950 Sludge Thickening 42 72 48 Sludge Dewatering 140 600 240 Disinfection 32 32 32 Buildings 200 200 200 Sludge Incineration 400 450 450 Sub Total $1,262 $2,732 $2,368, Contingencies (207 ) 250 550 470 Contractors Profit (lO0i ) 126 273 236 Engineering, Legal, Financial (l2%) 150 328 2.85 Total Cost $1,788 $3,883 $3,359 Design Basis: BOD Removal 90% 957 Suspended Solids 90% 957 1/ Table from D. G. Hager and P. B. Reilly, “Clarification—Adsorption in the Treatment of Municipal and Industrial Wastewaters.” Presented at the 42nd Annual Conference of the Water Pollution Control Federation Meeting in Dallas, Texas, October 5-10, 1969 (6). ------- 19 TABLE 11 OPERATING AND MAINTENANCE COST COMPARISONI’ 10 MCD Plant Activated Clarification Primary Sludge Adsorption BOD Removal 3570 9O7 9O7 957 Cents Per 1,000 Gallons Primary Treatment 3.3 3.3 3.3 3.3 Activated Sludge 2.2 Clarification Chemicals 0.3 0.3 Extra Sludge 0.1 0.1 Adsorption System 3.2 3.9 Sub Total 3.3 5.5 6.9 7.6 Incineration 2.6 3.6 3.8 3.8 Total /l,OO0 gallons 5.9 9.1 10.7 11.4 1/ Table from D. G. }tager and P. B. Reilly, “Clarification-Adsorption in the Treatment of Municipal and Industrial Wastewaters.” Presented at the 42nd Annual Conference of the Water Pollution Contro1 Federation Meeting in Dallas, Texas, October 5-10, 1969 (6). ------- 20 TABLE 12 TOTAL COST COMPARISONL” 10 MGD Plant Activated Clarification Primary Sludge Adsorption BOD Removal 357 90° ! , 9070 957 Cents per 1,000 Gallons Operating and Maintenance 5.9 9.1 10.7 11.4 Amortization of Capital 4.0 8.7 7.2 7.2 (57,--20 years) Total /1,O0O gallons 9.9 17.8 17.9 18.6 1/ Table from D. C. Hager, and P. B. Reilly, “Clarification-Adsorption in the Treatment of Municipal and Industrial Wastewaters.” Presented at the 42nd Annual Conference of the Water Pollution Control Federation Meeting in Dallas, Texas, October 5-10, 1969 (6). ------- 21 to carbon or for specialized application. At the present stage of de- velopment, adsorbent resins are not likely to replace carbon (7). Vanderbilt University is studying the properties of chemcoke, an apparently competitive material for activated carbon. The study will determine the ability of chemcoke to adsorb refractory materials (14). OXIDATION PROCESSES The Pacific Northwest Water Laboratory has investigated the ef- ficiency of oxidation ponds for removal of carbon from pulp and paper mill wastewaters (15). They found that for an unbleached Kraft pulp mill, the oxidation ponds removed approximately 60 percent of the TOC and COD and 90 percent of the ROD. For a sulfite pulp mill, the removals were 20 percent for COD, 32 percent for TOC and 73 percent for BOD. A variety of chemical oxidation processes have been investigated, such as chlorine catalyzed by ultraviolet light) metal catalyzed photo- oxidation, and ozone. Of these, only ozone appears to be technically feasible. Airco, Inc., is currently constructing a 50,000 gpd plant to determine its feasibility(4). ------- 22 BIBLIOGRAPHY 1. Weber, W. J., Jr., C. B. Hopkins, R. Bloom, Jr., “Physicochemical Treatment of Wastewater”. Journal Water Pollution Control Federa- tion , January 1970. 2. Bishop, D. F., L. S. Marshall, T. P. O’Farrell, R. B. Dean, B. O’Connor, R. A. Dobbs, S. H. Griggs, and R. V. Villiers, “Studies on Activated Carbon Treatment”. Journal Water Pollution Control Federation , February 1967. 3. Masse, Arthur N., “Removal of Organics by Activated Carbon”. Robert A. Taft Water Research Laboratory, August 1968. (Mimeo) 4. “Current Status of Advanced Waste- Treatment Processes”. Advanced Waste-Treatment Research Laboratory, Cincinnati, Ohio, July 1, 1970. 5. Beebe, R. L., and J. I. Stevens, “Activated Carbon System for Was tewater Renovation”. Water and Wastes Eng. , January 1967. 6. Hager, D. G., and Reilly, P. B., “Clarification-Adsorption in the Treatment of Municipal and Industrial Wastewater”. presented at the 42nd Annual Conference of the Water pollution Control Federation Meeting in Dallas, Texas, October 5-10, 1969. .7. Bishop, D. F., T.P. O’Farrell, and J. B. Stamberg, “Physical-Chemical Treatment of Municipal Wastewater”. Robert A. Taft Water Research Center, October 1970. 8. Rizzo, J. L. and R. E. Schade, “Secondary Treatment with Granular Activated Carbon”. Water and Sewage Works , August 1969. 9. Campbell, L. A., “Uptake of Dissolved Organic Carbon by Activated Sludge”. Water Pollution Control , October 1966, 104, No. 9. 10. Villiers, R. V., E. L. Berg, C. A. Brunner, and A. N. Masse, “Treat- ment of Primary Effluent by Lime Clarification and Granular Carbon.” Advanced Waste Treatment Research Laboratory, May 1970. 11. Parkhurst, J. D., F. 0.’ Dryden, G. N. McDermott, and 3. English, “Pomona 0.3 MGD Activated Carbon Pilot Plant”. presented at the 39th Annual Meeting, Water Pollution Control Federation, Septem- ber 29, 1966. 12. English, S. N., A. N. Masse, C. W. Carry, J. B. Pitkin, and J. E. Haskins, “Removal of Organics from Wastewater by Activated Carbon”. presented at the Advanced Waste Treatment Seminar, San Francisco, California, October 28-29, 1970. ------- 23 13. Clarke, 3., “How Color and Organic Carbon are Removed from Bleach Plant Effluent”. Pulp and Paper , February 1969. 14. Fisher, G. T., “Refractory Adsorption on Chemcoke”, School of En- gineering, Vanderbilt University, Nashville, Tennessee. (Research. Project Sponsored by FWQA). 15. Willard, H. K., Sanitary Engineer, Paper and Forest Industries. Memorandum dated February 3, 1971, to Jim Hatheway, DFI-DC. GPO 835-291 ------- |