United States
Environmental Protection
Agency
Municipal Environmental Researc,
Laboratory
Cincinnati OH 45268
 Research and Development
EPA-600/S2-81-173  Oct. 1981
Project Summary
Demonstration  Physical
Chemical  Sewage  Treatment
Plant  Utilizing  Biological
Nitrification
James F. Kreissl and Ronald F. Lewis
 This study involved the design, con-
 struction and operation  of a hybrid
 physical-chemical (P-C) biological
 treatment facility. Evaluation of this
 system was based on two factors: its
 utility as a transportable facility for
 interim high quality treatment of
 wastewaters at different locations and
 its value as a treatment concept to
 incorporate the best attributes of both
 methods (P-C and biological) of treat-
 ment.
   Although the system  produced  a
 consistent, high  quality effluent, its
 utility as a transportable  system was
 only partially demonstrated and its
 viability as a treatment sequence
 could not be confidently stated due to
 several design and operational prob-
 lems.
   This summary presents an overview
 of this joint USEPA-DHUD project.
   This Project Summary was devel-
 oped by EPA's Municipal Environmen-
 tal Research Laboratory, Cincinnati,
 OH, to announce key findings of the
 research project  that  is  fully docu-
 mented in a separate report of the
 same title (see Project Report ordering
 information at back).

 Introduction
   Experience has shown  that a need
 exists for flexible and efficient sewage
 treatment units able to meet the ever
 more stringent regulations imposed by
 government. Urban fringe developments
 are particular problem areas that
 outstrip the service ability of urban
 sewage authorities.
  Small housing, commercial, and
 public developments spring up beyond
 the range of central sewage transport
 systems and must have acceptable
 sewage treatment on  a permanent or
 temporary basis. Often, the temporary
 nature of the treatment facilities com-
 pounds the problem, resulting in heavy
 capital equipment outlays prorated over
 relatively short time perfods. The small
 size and nature of such development
 areas frequently provide flow variations
 that are not conducive to effective
 biological treatment. Daily, as well as
 seasonal, fluctuations  may be extreme
 in both hydraulic and organic loadings.
 The need for treatment processes that
 can be placed in service quickly and with
 a minimum of delay to meet strict
 effluent limitations  has long been
 recognized. Development areas  on
 urban  fringes frequently discharge to
 small  streams with neither little dry
 weather flow nor periodic high rainy
 weather flow and effluent limitations
 are generally based on the most
 extreme low flow conditions.
  This demonstration  project was
 conducted  to show that wastewater
 could be treated in a physical-chemical
 wastewater treatment plant employing
 a biological intermediate stage for
 oxidation of nitrogenous material to
 produce a  high quality effluent and

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provide different treatment levels to
meet a variety of effluent requirements.
The physical-chemical  plant chosen
was  of a modular design employing
high-rate processes which normally
facilitate a relatively speedy installation,
a  minimum  amount of lag time to
produce  the  desired effluent quality,
and ease of transport for relocation to
other critical areas when needed.
  The plant was located in the drainage
area of a planned  residential develop-
ment known  as Beechgrove Village in
the southern part of Kenton County,
Kentucky. The wastewater was domestic
in nature, with no commercial or
industrial sources.

Facility Description
  The  facility consisted of a modular
physical-chemical (P-C) wastewater
treatment plant which was skid-mounted
for ease of transport, an intermediate
biological nitrification tower, an equali-
zation  tank and a sludge holding tank.
Any of these ancillary units to the P-C
plant could be constructed of materials
which  would facilitate  relatively fast
startup at a new location. Sizing of the
plant components was based on a flow
of 190 cu m/d (50,000 gallons per day).
The treatment  process sequence con-
sisted  of screening, flow equalization,
chemical flash mix, flocculation, clarifi-
cation,  pH  control, biological nitrifica-
tion, filtration, granular activated carbon
adsorbtion, and chlorination. Excess
sludge from the clarifier was periodically
transferred to the  sludge  holding tank
from which settled solids were occa-
sionally transported  by  truck to  a
disposal site. A treatment process flow
schematic of the demonstration plant is
shown in Figure 1.


Influent Flow Control
   Wastewater  for the  demonstration
plant was taken from an existing man-
hole above the lift station serving the
Beechgrove  Village development. A
diversion dam within  the manhole
provided a flooded section from which
the demonstration plant was fed. In the
outlet  pipe (0.2 m in diameter) an air-
activated pinch valve was located in the
flooded pipe which, when activated by
liquid level controls in the equalization
tank, opened and allowed diversion of
the wastewater to the  demonstration
facility through the 845-m gravity line.
The level controls were of  the solid-rod
type  located  directly in  the  main
equalization  basin. Signals from the
electrodes  were  transmitted via a
telephone circuit to a solid-state control
relay located near the pinch valve. The
relay in turn controlled a 3-way solenoid
valve which was installed in an air pipe
between the pinch valve and  an  air
compressor. The air pressure in turn
activated the pinch valve. Excess waste-
water  flow was discharged to the
existing  sewer from the  manhole
overflow.


Flow  Equalization Tank and
Screening
  A bar screen with approximately 25
mm (1-in) openings was located in the
influent structure of the flow equaliza-
tion tank to remove larger objects that
might  damage  the system.  The flow
equalization tank consisted  of  a rec-
tangular 75.7-cu  m (20,000-gal) pre-
fabricated coated  steel tank and  in-
corporated  a  diffused-air system to
ensure solids  suspension and mixing
and also to maintain aerobic conditions
during storage. The buffer capacity of
this tank allowed continuous operation
during  normal low flow conditions
encountered  at night. The  tank also
received filter and adsorber spent back-
washes. In addition to the influent flow
control liquid-level sensors, electrodes
were also installed to provide emergency
shut down of the remaining treatment
processes in the  event  of  low level
conditions in the flow equalization tank.
The wastewater was pumped from the
flow equalization tank to the treatment
unit by a constant-speed,  progressive-
cavity pump.

Chemical Clarification
  Chemical  clarification was achieved
using hydrated  line fed at a periodically
adjusted constant rate in a 10 percent
slurry form. Lime slurries were made up
on  a  daily basis using  commercial
hydrated lime in 22.7 kg (50 Ib) bags. A
1.363-cu m (360 gal) plastic tank served
as the makeup and storage tank. Con-
stant  mixing  of  the lime tank was
provided to maintain the slurry using a
0.37 kw (0.5 hp) constant-speed mixer.
Lime slurry was fed to the 0.25-cu m
j(65-gal) flash-mix tank using a variable-
speed, diaphragm-type slurry metering
pump. A constant-speed mixer provided
thorough mixing of the lime slurry with
the  incoming  wastewater from  the
equalization tank. Theoretical detention
time within the flash mix unit was 1.87
minutes at the design flow rate of 190
cu m/d (50,000 gal/d).
  Flocculation was provided in a square-
shaped 2.16-cu m (570-gal) tank. J
Agitation was carefully controlled using [
a variable-speed, vertical-shaft mixer.
Theoretical detention time was 16.2|
minutes at design flow rate.
  Flow from the flocculation tank was!
introduced to the 17.83-cu m (4,710-
gal) circular clarifier through a distribu-
tion box which channeled the flow to a I
peripheral-feed inlet near the bottom of I
the clarifier. A  theoretical detention!
time of 135 minutes was available in the I
clarifier at the design overflow rate of 261
cu m/sq  m/d (640 gal/sq ft/d). The!
design, overflow weir rate was 21  cul
m/m/d (1,700 gal/ft/d). The clarifierj
was equipped with motor-driven sludge!
raking  and skimming and an  effluent!
"V-notch" weir around the circumfer-f
ence of the tank.

pH Control
  A neutralization step was necessary!
following  lime clarification in order tol
prevent deposition of calcium carbonate!
in subsequent processesand to facilitate!
the biological nitrification process. For!
large-scale systems this is  often ac-l
complished by recarbonation of the high!
pH  clarified wastewater with carbon!
dioxide (COz). For this facility, sulfuric|
acid was  used because of the capita
cost and space savings inherent in this
approach.
  Sulf uric acid was purchased in 49- orl
57-liter (13- or 15-gal) plastic carboys,!
and the required solution was made up!
daily. A 0.3-cu m (80-gal) plastic tank!
was used for mixing and storage of the!
20% sulfuric  acid  solution. A small!
mixer  was  installed in this tank  tol
ensure the initial blending of the water!
and acid. A variable-speed  chemical!
feed pump  was used  to transfer the!
solution  to the  0.19-cu m (50-gal)|
neutralization tank for the lime-clarified!
effluent.  Thorough  mixing of the acid I
feed solution and high-pH effluent was!
provided. The tank was equipped with!
electrodes for  pH measurement which!
provided signals to the pH control unit!
which, in turn, controlled the off-onj
operation of the acid feed pump. Experi-l
ence  demonstrated that acid added!
directly into the clarifier effluent piping!
upstream of the baffled neutralization
tank (baffled to separate the mixing and I
sensing functions)  were necessary tol
obtain  satisfactory  operation.  The
neutralization  tank  effluent  was then
pumped to the nitrification towers
during most of the operational period, I
even though flexibility was available to I

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                                                 Chemical Feed
 Influent
                                                      Mix    I  *
                                                   ^  Tank J
                                                        Activated
                                                        Carbon
                                                        Columns
 Figure 1.    Demonstration plant process flow schematic.
vary the sequence of all subsequent
processing steps.

Biological Nitrification
  Three separate biological nitrification
towers were constructed from 1.85-m
(72-in) diameter concrete pipe sections.
Overall height of each unit was 5.18-m
(17-ft), and they were packed to a depth
of 4.57-m (15-ft) with a high specific
surface plastic media which was light-
weight and  provided 187 sq m/cu  m
(57-sq ft/cu ft) of surface area with 93
percent void space and a bulk density of
64  kg/cu m (4  Ib/cu  ft) by virtue  of
random packing in the towers.
  The three nitrification units were
designed for parallel operation, with
adjustable flow rates to each unit. The
system design allowed for total recycle
of "seed" sludge in order to obtain a
biological population capable of effecting
nitrification within a reasonable period
(4 to 6  weeks) after  startup.  Rotary
distributor arms were used in each
tower to provide uniform  surface
distribution. The underdrains from each
tower discharged to a  commom sump
for pumping to the subsequent process.
Based on the 7.88 sq  m (84.8 sq ft) of
surface  area contained in the three
towers, the design surface loading rate
was 9.8 cu  m/sq m/m  (0.4  gal/sq
ft/m).
  As with all processes following
clarification/neutralization steps, ef-
fluent from the  nitrification  towers
could be directed to  the dual-media
filters or to the  granular activated
carbon adsorption towers; the former
scheme  was  used throughout  this
study. System design was based on the
presumption from earlier pilot studies
that there would be a low net solids
production associated with the nitrifica-
tion towers so that intermediate clarifi-
cation  prior  to filtration would not be
required.

Dual-Media Filtration
  The  filter  used  was  a downflow
pressure system employing the  dual-
media concept, i.e.,  a 0.3-m (1-ft) layer
of AWWA B  100 medium (0.45 to 0.55
mm effective size) sand overlain by a 0.3
m (1 ft) layer of anthracite, AWWA B100
No. 1 (0.6 to 0.8 mm A 1.6-cu m)  (424-
gal) surge tank preceded the  pressure
filter and provided flow storage during
the filter backwash cycle. In  addition,
the surge tank was equipped with liquid
level sensors that served as controls for
the pressure filter feed pump. Flow rate

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through  the 0.66-sq  m  (7.1-sq  ft)
surface area filter was controlled by a
variable orifice, pressure-compensated
flow regulator at 12.2 cu m/sq m/h (5
gal/sq ft/m). Backwash operation was
automatic with intervals between back-
wash cycles being operator selectable
on a  24-hour  time clock.  The manu-
facturer suggested backwash initiation
at 28 to 35 k Pa (4 to 5 psig) pressure
differential  across the pressure filter.
This corresponds to a  head loss of
between 2.8 and 3.5 m (9.2 and 11.5ft).
Flexibility also existed for controlling the
length of each backwash sequence. The
chlorine  contact tank  served as the
backwash source, and backwashing
flow was regulated through a constant-
flow control valve at a rate of 43  cu
m/sq m/h  (17.7 gal/sq ft/m).  To
facilitate  backwash efficiency, a pre-
backwash air source was provided.
Spent backwash was returned to the
flow equalization tank.

Granular Activated Carbon
Columns
  Two granular activated carbon columns
were used to provide  removal  of
dissolved organic matter.  The two
columns were  operated in series with
the first column  being an  upflow type
and  the  second  being of downflow
design. Empty-bed contact time for each
column was approximately 21.6 minutes.
Each  1.22-m (4-ft) diameter by 2.44-m
(8-ft) tall column  contained  approxi-
mately 1.22 m(4-ft)of granular activated
carbon (Calgon Filtrasorb 300) underlain
by a 0.3-m (1 -ft) layer of selected gravel.
Flow  was introduced into the upflow
column via a perforated distributor
buried in the supporting gravel layer. In
order to maintain a fluidized condition in
the carbon bed at the liquid upflow rate
of 6.8 cu m/sq m/h (2.8 gal/sq ft/m), a
stream of air was also introduced at a
manually controlled rate through a
second perforated distributor within the
gravel layer. Overflow from the upflow
carbon column  was screened prior to
overflow to the surface of the downflow
column. Backwash facilities similar to
those for mixed  media filtration were
incorporated in the design of the down-
flow carbon column. The backwash flow
rate was 19.5 cu m/sq m/h (8.0 gal/sq
ft/m), and a surface wash was provided
during the backwash cycle. The chlorine
contact tank also served as the backwash
water source for  this  operation,  and
spent backwash was returned to the
equalization tank.
Effluent Subsystem
  The effluent subsystem included  a
water meter for recording plant effluent
flow and the chlorination facilities for
disinfection of the final effluent. A 4.46-
cu m (1,178-gal) chlorine contact tank
provided a theoretical contact time of
33.6 minutes  at  the design  flow.
Chlorine was fed from a 45.4 kg (100 Ib)
liquid chlorine cylinder using a solution-
feed, vacuum-operated gas chlorinator,
mounted directly on the cylinder. The
operating vacuum  was provided  by  a
hydraulic  injector  unit, with a close-
coupled  diffuser attached to a  sub-
mersible pump mounted on the contact
tank floor.


Sludge Handling Facilities
  A 30.28-cu m (8,000 gal) rectangular
sludge storage  tank  was  provided to
handle the excess lime sludge from the
chemical  clarification  unit. As  lime
sludges  generally show good settling
properties, provisions were made in the
storage  tank to gravity  thicken  the
sludge. Supernatant drawoff ports were
placed at selected elevations along the
upper section of the sludge storage tank
to allow decanting  of the supernatant
during settling. The decent was returned
to the flow equalization tank.
  A diffused-air system was installed to
prevent  anaerobic  conditions  and ex-
cessive  compacting  and to facilitate
removal of the thickened  sludge. Cou-
plings were  installed at the bottom
sludge draw-off valve toallow tank truck
disposal of excess accumulated solids.
The  design  and intent of the sludge
storage-thickening  unit was to aerate
the sludge to prevent anaerobic condi-
tions and to periodically stop aeration to
permit  thickening and  subsequent
supernatant  drawoff. Withdrawal of
thickened solids  for disposal  was
permitted only during the aeration cycle
to assist in fluidizing the tank contents
for easier withdrawal.
Evaluation Factors

Sampling
  Automatic composite samplers were
used  for collecting  samples from the
equalization  tank (influent) and the
effluent from the carbon adsorbers prior
to chlorination (effluent). Also, periodic
grab samples were taken of the clarifier
effluent, neutralization tank effluent,
nitrification tower effluent and filter
effluent. All samples were refrigerated
including samples for biochemica
oxygen demand (BOD5) and suspended
solids (SS).  Besides  refrigeration
samples for chemical oxygen demand
(COD), total organic carbon (TOC), tola
Kjeldahl nitrogen  (TKN),  ammonia
nitrogen (NH3-N) nitrite  nitrogen (N02
N),  nitrate nitrogen (NO3-N), acid
hydrolyzable phosphate (AHP), and
orthophosphate were further preserved
by the addition of 2 ml of H2S04 per lite
of sample  following  collection. Al
testing was done in  conformance with
"Standard Methods for Examination o
Water and  Wastewater," Fourteenth
Edition, 1975.

Construction and Start Up
  Project planning and plant design an
specifications were  completed in Feb
ruary 1975. Due to the nature of th
project and the equipment required, tw
separate contracts were awarded. On
contract encompassed the skid-mountec
physical-chemical treatment system,
while  the  other covered site work
nitrification towers, the flowequalizatio
tank, the sludge storage/thickene
tank, and other miscellaneous items. A
bids for both contracts were considerabl
in excess of  the budget limits of th
project.  Negotiations with the lo\
bidders coupled with numerous desig
changes resulted  in  the  eventual
signing  of  both contracts within th
original budget estimates. The physical
chemical (P-C)  plant was delivered  i
January 1976.  The  work scheduled  i
the second contract was to be complete
in late  November 1975,  but due  t
financial difficulties on  the part of th
contractor  and subsequent  unantici
pated requirements  resulting from thi
problem, the construction phase an
initial testing were not completed unt
late 1977.
  Numerous  problems  were encoun
tered during the initial attempts to chec
out the individual units  in the system
and to verify their proper operation. Th
treatment  system was designed fo
above ground operation  to allow for
short installation time and to facilitat
movement  of  the  system to anothe
location, should the need arise. The P-C
system  was  delivered  to  the site  ir
January 1976.  Because  of the seriou
delays  in  completion  of the othe
contract, this equipment was left at th
site, unused, for two years  including
two winter seasons of unusually cold
weather. Proper precautions were not
taken to  protect the units during this

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 long period.  Numerous pipes, valves,
 fittings, and pumps suffered substantial
 damage,  requiring  replacement or
 repair. Breakdowns encountered with
 pumps and motors continued to be a
 major problem during the entire opera-
 tional phase  of  the  project,  probably
 caused by the long exposure.

 Results

 Overall Removals
  Prior to system design 10 twenty-four
 hour  composite  samples  of  the  raw
 wastewater gave the results presented
 in Table 1.
  During  the operational phase, the
 average BOD5 of the equalization tank
 samples average characteristics were
 159 mg/l of BOD5,368  mg/l of SS, and
 435 mg/1 of COD, as shown in Table 1 in
 parentheses.  The  significance of the
 differences between these values is not
 clear, since some are lower and some
 higher. Certainly, some changes could
 be due to the aerated flow equalization
 tank  prior to the pumping  to  the
 clarification unit. Since the theoretical
 retention time in the equalization tank
 was between 5  and 10 hours, some
 biological oxidation could have occurred,
 and the recycle of certain streams from
 the treatment system to this tank would
 also account for some variance.
  A summary of the treatment  efficien-
 cies achieved with each of the units
 (clarifier, nitrification tower, dual-media
 filtration,  and  carbon columns) is
 presented  in  Table 2.  The percent of
 removal of BOD5, COD, TOC, SS, acid-
 hydrolyzable  phosphorous, and  total
 nitrogen, is presented. The data represent
 paired samples  where influent and
 effluent samples  were taken from each
 unit and analyses performed. Thus, the
 percentage of removal within one unit is
 calculated from the difference of  the
 influent and effluent  of that unit. The
 percentage of cumulative  removal is
 calculated  from the difference between
the  clarifier influent and the effluent of
that unit. As can be seen, the removals
of BODs,  COD,  TOC  and SS were
 excellent,  with cumulative removals
 ranging from 88 percent for COD to 97
percent for suspended solids.  The
greatest amount of organic material and
suspended  solids was removed during
the  lime clarification.
  Phosphorus removal from an influent
 concentration average of 12.3 mg/l was
 also excellent but the nitrogen  removal
was rather low. The major portion of the
 phosphorus was removed during the
 lime clarification. High lime feed with a
 higher pH (11.4 as compared to 10.7 for
 the low lime feed) significantly increased
 the removal of phosphorus, i.e., from 63
 to 87 percent. Recycle or non-recycle of
 clarifier sludge had little influence on
 the removal of phosphorus.
  Nitrification never properly developed
 during the course of the study, even
 though nitrogen removals averaged 40
 percent from the average influent con-
 centration  of 38 mg/l  during the last
 eight weeks of operation. The overall
 removal of nitrogen  averaged 32 per-
 cent, with losses nearly equally split
 between the clarification, filtration, and
 carbon adsorption processes. In the first
 two processes these removals can be
 attributed to the  organic  nitrogen
 content of the solids removed. In the last
 process nitrogen removal appears to
 have been due to denitrification in the
 carbon beds.

 Individual Process Performance
  As noted in Table 2, the lime clarifica-
 tion  step  accounted  for the  major

Table 1.    Wastewater Characteristics*
portion of removal of all pollutants
measured.  From the  standpoint of
defined secondary effluent quality, the
clarifier effluent nearly met the BOD5:SS
requirement of 30:30, with  actual
values of 46:21. Organics, as measured
by BODs, COD and TOC were removed
by average rates of 66 to 77 percent,
while 82 percent of the acid-hydrolyzable
phosphorus was removed.
  The nitrification tower, though seem-
ingly ineffective in its intended  role as
measured by nitrogen series analysis,
did provide  significant additional re-
movals of BOD5, TOC and COD. The
reasons for the apparent lack of nitrifi-
cation remain somewhat mystifying
based on earlier published data which
indicated that the  designed system
should be able to oxidize 3.2 to 8.2 kg of
NH4-N/day (7 to 18 Ib/d). Since the
approximate loading was 5.0kg  of Nt-U-
N/day (11.0 Ib/day),  the resulting
oxidation, as measured by NO2-N and
N03-N increase, of  0.27 kg/day (0.6
Ib/day) was disappointing. This is
especially true in  light of favorable
wastewater  temperatures and  BOD5/
 BOD5   COD  TS      VTS    SS    VSS   DS    VDS   pH     Alkalinity
                                                                  as CaCO3

 239    370   974    467    411    219    562    248   7.0     278
 (159f  (435f	(368)*	

 *  all analyses in mg/l, except pH
 *  operational phase averages
Table 2.    Project Data Summary
                                    Parameter Measured*
Subsystem
Clarifier
% Removal
% Cumulative
Nitrification
% Removal
% Cumulative
Dual-Media Filter
% Removal
% Cumulative
Carbon Columns
% Removal
% Cumulative
BODs

77
77

44
84

—
91

33
93
COD

73
73

13
76

4O
86

15
88
TOC

66
66

42
80

5
82

20
86
SS

86
86

Neg.
85

71
95

39
97
AHP**

82
82

Neg.
80

17
85

Neg.
80
77V***

13
13

Neg.
11

11
24

10
32
    Data represents paired samples where influent and effluent analyses were
    performed.
    Acid-Hydrolyzable phosphorus
   1 Total Nitrogen

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TKN ratios. Initial attempts to provide
seeding to the nitrification towers were
unsuccessful due to hydraulic deficien-
cies in the plant, but sufficient operating
time was available for natural develop-
ment of nitrifiers. The fact that no such
development took place wou Id appea r to
be due to either the unreliability of the
neutralization step and/or the  lack of
recirculation.
  The  dual-media performed well  in
terms of solids removal and concomitant
removals  of organics, TKN and  AHP
associated with those solids. Suspended
solids  removals of 70 percent were
achieved,  along with COD, TOC, TKN
and AHP removals of 40, 5, 11  and 17
percent,  respectively.  However, the
media  sizes were not well-suited  to
handling the 44 mg/l  of SS  (average)
found in the filter influent. Therefore,
filter runs were frequently as short as
four hours, which represented a con-
siderable 0/M problem, because of the
fine coal size provided with the  filter.
  The activated carbon columns were
loaded very lightly during this study. The
COO removed by the adsorbtion process
had reached 0.18 Ib. of COD  per Ib. of
activated  carbon by the end  of the
project, no apparent  reduction in the
rate of COD removal verified that the
carbon had not been  exhausted. The
system was designed with the capability
of removing spent carbon and adding
fresh carbon. Denitrification  of the
nitrate produced by the nitrification
towers did occur in the carbon columns,
and no hydrogen sulfide problem was
encountered.

Performance Reliability
  In spite of the equipment and opera-
tional problems encountered, the hybrid
(physical-chemical/biological) treat-
ment plant, as designed, was  able to
produce a consistent, high-quality
effluent, when compared to  typical
biological systems used to treat waste-
waters from small communities. Figure
2 compares the reliability of this hybrid
system for the removal of BOD5 and SS
versus extended aeration plants in the
Cincinnati area. Since this hybrid plant
also removes phosphorous, other bio-
logical  systems would require ancillary
treatment steps to provide comparable
performance characteristics.

Operation and Maintenance
  The  normal  operation and mainte-
nance  of this plant was  more  time
consuming and complex than that
associated with most  biological treat-
  ;oo
                                                                    ;oo
    o
                JO    20  30  40 50 60  70  80   90  95   98  99

                     Percent of Time Value was Less Than

figure 2.    Comparison of BODs and SS reliability.
ment plants. Some of the work involved
the sampling and  laboratory testing
required at the site for the experiments
of this project  and included sample
preparation and delivery and prepara-
tion of logs and records. However, there
were a number of pumps, tanks, mixing
chambers,  and backwash  systems
which had to be cleaned, adjusted, and
occasionally repaired.  The  mixing  of
chemicals (lime slurry and acid neutral-
izer) required knowledge of the opera-
tions and caution  to avoid  chemical
burns. One full time  operator was
required with additional manpower
required for any unusual  problem.
Weekend coverage of the plant was also
provided.

  In order to properly conceive of the
0/M requirements,  it should be noted
that an extended aeration package plant
capable  of handling the same design
flow normally requires approximately
0.5 person-years/year. Therefore, the
manpower required  for the  hybrid
system was approximately three times
that required for an extended aeration
system.  Likewise, increased chemical
costs are inherent to the hybrid system
design. The value of relatively instan-
taneous, high-quality effluent would
have  to  be weighed  against  these
increased O/M costs on a case-by-case
basis. The question  of  initial cost
comparison is far more difficult because
of the transport-ability of the physical-
chemical portion  of the hybrid  plant.
Multiple  use  of such  a system  by a
public or private entity at different sites
would determine whether  such a
system would be economical.

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Discussion
  Two factors were intended for testing
in this study, the technical feasibility of
the treatment sequence and the concept
of transportability. Although certain
shortcomings  arose  in  the testing of
these factors, certain implications of the
study are relevant to each.
  The transportability concept is impor-
tant to agencies such as DHUD in that
the  potential  health and ecological
dangers which often result from natural
or man-made disasters might be mini-
mized  through prompt response with
nearly instantaneous high quality treat-
ment capability to meet  most water
quality limitations. To a lesser degree,
an  adjunct treatment  capability  for
"boom towns" or  other sudden popula-
tion increases, which in recent times
have been associated with energy
development, could obviate the potential
impacts  on a fragile ecology due  to
sudden overload  of  existing  sanitary
facilities and infrastructure.
  As noted earlier, the physical-chemi-
cal (P-C) portion of the hybrid treatment
plant was skid-mounted and trans-
portable from  site-to-site by tractor
traitor. The  associated process needs,
i.e.,  equalization and sludge handling,
could quickly be provided at almost any
site by excavation and lining or other-
wise sealing  of  the soil to  prevent
seepage and/or introduction of debris
to the wastewater, if such tankage is not
already available. Therefore, a complete
(P-C) unit could be quickly operable at
such locations, assuming necessary
power provisions  at the plant site. The
nitrification tower is an unlikely addition
in the event that a nitrogen  standard
must be met, not because of its marginal
performance during  this study, but
because its inherent lag time to reach
proper nitrification is inconsistent with
the otherwise quick startup potential of
the  unit. Therefore,  the P-C system
alone would serve the transportability
function  quite well if  no nitrogen
standard were in effect and offer the
added  benefits of phosphorus removal
and consistently high quality  perform-
ance. Introduction of a nitrogen standard
would probably require the use of break-
point chlorination  or stripping towers in
order to provide relatively instantaneous
nitrogen removal consistent with the
overall plant characteristics.
  The technical feasibility of the hybrid
facility's processing sequence  is a
separate issue. The concept of utilizing
biological nitrification with physical-
chemical processing was designed to
overcome two basic weaknesses in the
P-C treatment concept, i.e., high NI-U-N
concentrations in the effluent and odors
associated with the carbon adsorbers.
the perceptible nitrification was minimal,
the total system did remove about 30
percent of the nitrogen in the waste-
water,  as  opposed  to  the original
estimate of  36 percent. The major
The latter problem had been overcome
by the addition of NOa-N to the influent
of carbon adsorbers in sufficient quantity
to prevent  H2S formation. The hybrid
facility was  designed  to utilize  the
nitrogen already in the wastewater by
converting, all or part of, it to the N03-
form prior to carbon adsorption. Although
difference in the  actual vs.  estimated
effluent quality was  the  form of  the
nitrogen, i.e., NH4-N rather than N03-N,
which could  result in a  significant
oxygen demand in the receiving stream.
  The overall acceptability of a waste-
water treatment system is  based on a
variety of factors including  capital and
O/M costs, labor requirements and
performance  characteristics. If one
assumes that  the  reasons for poor
nitrification tower performance can  be
easily overcome through  improved
neutralization and nitrification tower
design, the hybrid design studied (with
proper  filter  media)  is  capable  of
producing a high-quality effluent un-
matched by either  pure biological  or
pure physical-chemical systems, incor-
porating  the positive features  of both
systems, e.g., compact size, reliability,
resistance  to  toxic  upset, improved
toxics removal, phosphorus removal,
non-odorous operation, and nitrogen
reduction with ammonia removal.
  The EPA authors James F. Kreissl fa/so the EPA Project Officer, see below) and
    Ronald F. Lewis are with the Municipal Environmental Research Laboratory.
    Cincinnati, OH 45268.
  The complete report, entitled "Demonstration Physical Chemical Sewage Treat-
    ment  Plant Utilizing Biological Nitrification," was authored by E. Brenton
    Henson of the Sanitation District No. 1 of Campbell and Kenton Counties,
    Covington, KY 41 Oil fOrder No. PB 82-101 643;  Cost: $9.50, subject to
    change} will be available only from:
          National Technical Information Service
          5285 Port Royal Road
          Springfield,  VA 22161
          Telephone: 703-487-4650
  The EPA Project Officer can be contacted at:
          Municipal Environmental Research Laboratory
          U. S. Environmental Protection Agency
          Cincinnati, OH 45268
                                                                    •fr U. S. GOVERNMENT PRINTING OFFICE: I98I/559-092/332I

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