-------
Table 3
Unit Process and Equipment Data
Equipment
Raw Sewage Pumps
Primary Clarifier
RBC Units
RBC Effluent Pumps
Secondary Clarifiers
Chlorine Contact
Primary Digester
Secondary Digester
Tank Truck
Drying Beds
Liquid Alum Storage
Design Data
30 1,400 gpm (88.3 I/sec), 2
variable speed, 1 constant speed
lag pump
1 rectangular 70,000 gallon (265
cu m) capacity with 1.5 hr.
detention and 895 gpd/sq ft
(36.5 cu m/day/sq m) overflow
rate
Bio-Surf by Autotrol. Two
parallel paths with three shafts
and six stages in each, 515,500
ft2 (47,890 sq m) of media,
90 minutes retention and 1.94
gpd/sq ft (0.097) cu m/day/sq m)
hydraulic loading rate
Same as raw sewage pumps
2 rectangular, 2.75 hr detention
and 620 gpd/sq ft (25.3 cu
m/day/m2) overflow rate
2 baffled tanks, 35 min reten-
tion
1 fixed cover, 100,000 gal
(378.5 cu m) capacity with 15.5
days detention at design
loading, heated, mixed by gas
recirculation
1 floating cover, 100,000 gallon
(378.5 cu m) capacity with
supernatant discharge to raw
wastewater wet well
1 2,500 gallon (9.4 m3)
capacity
Adjoining sanitary landfill
site, 600' x 200' (183 m x 61 m)
without underdrains
2 tanks, each 2,600 gallons (9.8
cu m) capacity
96
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clarifiers. Secondary effluent is chlorinated prior to
discharge to Lake Michigan.
Grit is manually cleaned from the grit chambers and disposed of
at a sanitary landfill. Settled primary and secondary sludges
are pumped to a primary anaerobic digester that is heated and
equipped with gas recirculation and mixing apparatus. Settled,
digested sludge from the secondary digester is withdrawn by tank
truck to sludge drying beds off-site. Dried sludge is disposed
of in a sanitary landfill. Supernatant from the secondary
digester is drained by gravity to the raw wastewater wet well.
INITIAL OPERATING EXPERIENCE
The operation of the plant was begun on March 1, 1974. At the
same time, an 18-month testing and shakedown program was begun
to monitor the performance of the plant and to make operational
improvements where necessary. During this period, wastewater
flows averaged 0.755 mgd (2,875 cu m/day) and were influenced
occasionally by sewer infiltration and inflows. At start-up,
wastewater temperatures averaged 45°F (7.2°C), then gradually
increased to the low 60's (°F) by mid-summer.
Influent BOD-5 concentrations ranged from 129 to 219 mg/1 and
influent total suspended solids concentrations ranged from 101
mg/1 to 168 mg/1. The average influent BOD-5 and total
suspended solids concentrations for the test period were 164
mg/1 and 132 mg/1, respectively.
97
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The results of the initial 18-month test period are summarized
as follows:
Because the influent wastewater temperatures were quite
cold at start-up, it took 18 days before heavy sloughings
of biomass were observed and several months to achieve a
steady state operation.
During the last 12 months of the testing period (September
1974 through September 1975) with the addition of 70 mg/1
of alum and 0.8 mg/1 of polymer, effluent BOD-5's were
generally less than 10 mg/1; effluent suspended solids
averaged 15 mg/1; and effluent total phosphorus con-
centrations were less than 1.6 mg/1.
In January 1975, design flow conditions were simulated for
two weeks by shutting down one of the parallel RBC paths
and one of the final clarifiers. The effluent BOD-5 for
this two-week test period averaged 19 mg/1, while the
average wastewater temperature was 47°F (8.3°C).
Because of low hydraulic loadings (1.0 to 2.1
nitrification occurred; 50% to 60% reductions in ammonia
nitrogen occurred during the winter months and 85% to 95%
reductions occurred during summer months.
After one of the RBC paths was restarted in February 1975,
after being shut down for full scale tests, nitrifiers did
not re-establish dominant cultures on latter stages until
June, when wastewater temperatures approached 60 °F
Excellent BOD-5, suspended solids and ammonia nitrogen
removals permitted reductions in effluent chlorine doses,
from 6-7 mg/1 to 2-3 mg/1.
Recycling of secondary sludge through the primary clarifier
was required to thicken the combined sludges from 2% - 3%
solids to 4% - 5% solids content.
Slug releases of digester supernatant to the head end of
the plant were detrimental to overall nitrification
results. Controlled release of digester supernatant is
considered essential to achieve consistent ammonia
nitrogen reduction.
No significant differences were noticed in the digesti-
bility of sludges with or without alum addition. Phos-
phorus release, volatile solids reduction, or gas
production were not significantly affected by alum
addition. The average total sludge production was 0.83 Ib
of total solids per pound of BOD-5 removed. This figure
takes into account chemical sludge production.
98
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The measured power usage by the rotating biological
contactor shafts ranged from 5.6 hp to 3.5 hp. The average
running horsepower per shaft was 4.2 hp.
PLANT PERFORMANCE (1976-1979)
The overall performance of the plant, subsequent to the 18-month
test program, is summarized in Table 4. The data covers the
period from January 1976 through December 1979. Table 5 shows a
comparison of plant performance under summer and winter con-
ditions. Data for these tables was obtained from the monthly
operating reports prepared by the plant operators.
This data shows that the plant is consistently removing over 90%
of influent BOD-5 even under winter conditions and at hydraulic
loading rates of between 1.0 and 1.4 gpd/ft2. Wastewater
strength is affected by increased infiltration and inflow during
warm weather months. During winter months, effluent BOD-5
concentrations increase as wastewater temperatures decrease to
lows of 45°F. Effluent dissolved oxygen concentrations are
consistently above 7 mg/1.
Effluent total suspended solids concentrations remained fairly
consistent throughout the period at an average of about 16 mg/1.
The hydraulic profile of the plant is such that secondary solids
are pumped twice prior to removal with settled primary solids.
The addition of polymer assists secondary sedimentation, and
lower suspended solids concentrations could probably be obtained
in the final effluent if flocculants were not disturbed by the
centrifugal pumps.
99
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Table 4
Performance Summary
Parameter
1976
- - Annual Averages •
1977 1978
1979
BOD-5 (mg/1)
-Influent
-Effluent
-% Removed
TSS (mg/1)
-Influent
-Effluent
VSS (mg/1)
-Influent
-Effluent
Total Phosphorus (mg/1)
-Influent
-Effluent
-% Removed
Ammonia-N (mg/1)
-Influent
-Effluent
-% Removed
Eff. Dissolved Oxygen (mg/1)
Raw Sludge Pumped (Ib VSS/day)
Digester Gas Prod, (cu.ft./day)
Chemicals Used (Ib/day)
-Chlorine
-Alum
-Polymer
182
6
97%
135
15
111
8
7.8
1.4
82%
7.3
576
4,307
13
435
1.5
1
6
1
15
3
7
.725
.41
143
7
95%
122
16
95
7
.3
.1
83%
.5
.5
77%
.6
544
3,981
19
485
.612
1.19
155
7
95%
139
17
112
8
4.7
0.9
81%
17.4
2.1
88%
7.6
512
3,954
12
365
.712
1.38
129
12
91%
118
16
92
9
3.5
0.9
74%
15.9
2.0
87%
8.2
544
3,718
12
262
1.7
1.5
1.4
100
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Table 5
Comparative Performance Summary
Winter vs Summer Operation
Average Winter Average Summer
Values I/ Values 2/
Flow (mgd) 0.530 0.726
Hydraulic Loading (gpd/sq.ft.) 1.03 1.41
Waste Temperature (°F) 46 64
BOD-5 (mg/1)
-Influent 181 128
-Effluent 10 9
-% Removed 94 93
TSS (mg/1)
-Influent 140 130
-Effluent 16 16
Total Phosphorus (mg/1)
-Influent 5.8 4.7
-Effluent 0.8 1.0
-% Removed 86 79
Ammonia-N (mg/1)
-Influent 20.0 15.1
-Effluent 4.9 1.0
-% Removed 76 93
Effluent Dissolved Oxygen (mg/1) 8.1 7.3
\J From January, February, March, 1977 through 1979 reported data.
2/ From July, August, September, 1977 through 1979 reported data.
101
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More than 80% of influent total phosphorus concentrations are
removed by the addition of alum (hydrated aluminum sulfate).
Plant operators attempt to maintain a liquid alum dosage rate
sufficient to provide 1.5 moles of aluminum to 1.0 mole of
influent total phosphorus.
The plant was not designed to accomplish nitrification.
However, because it is currently operated at hydraulic loadings
of less than 2 gpd/ft^, nitrification does occur. Ammonia
analyses show that average influent ammonia concentrations of 16
mg/1 to 18 mg/1 are reduced to 2 mg/1 to 4 mg/1 through the
plant. As might be expected, less nitrification occurs during
winter months.
In 1979, an average of 710 pounds per day of sludge was pumped
to the primary digester with an average solids content of 3.7%
by weight. The volatile content of the sludge averaged 74% by
weight. Total sludge production, including chemical sludges,
averaged 1.14 pounds per pound of BOD-5 removed, or approxi-
mately 1,000 pounds per million gallons treated. Approximately
262 pounds per day of alum was added to remove an average of 2.6
mg/1 of total phosphorus.
OVERALL OPERATIONS AND MAINTENANCE
The Gladstone plant is staffed by one superintendent and three
shift operators. The plant is manned 16 hours per day, five
days a week; eight hours per day on week-ends and holidays. The
superintendent also has the responsibility of the water
filtration plant, staffed by two operators. Most of the
102
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operators are cross-trained to provide flexibility. All opera-
tors are state certified and operate shifts on a rotational
basis.
All laboratory tests are conducted according to "Standard
Methods", 14th edition.
Flows are measured weekly at the Parshall flume to check the
flow meter. The chlorinator, sampler, alum and polymer feeders
are regulated by the flow meter.
Secondary sludge is returned at least five times per day to the
primary clarifier to thicken the combined sludges from 2%-3% to
4%-5% solids content. The combined sludge is then pumped to the
primary anaerobic digester. Digesting sludges are monitored
weekly for volatile acid/alkalinity relationships and volatile
content. When the volatile percentage is less than 50% and the
supernatant shows excessive solids, sludge is hauled by tanker
to the drying beds. The digesters are cleaned and inspected at
three year intervals.
The RBC units are greased at the main bearings twice per week
with 5 to 6 shots of grease. The oil in the chain casings and
speed reducers is changed yearly or more often if the oil should
become diluted with water. The walkways and the area around the
disks are scrubbed weekly. The tanks are drained and flushed
yearly for a general inspection. Very little accumulation has
ever been found. The three V-belts on the drive units are
replaced about yearly upon breakage. One main shaft bearing
failed in the six years of operation.
103
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The plant staff also maintains the six lift stations throughout
the 22 miles (35.4 km) of the collection system, which ranges in
size from 4 inches (10.2 cm) to 3D inches (76.2 cm). Most of
the collection system was installed during the 1920's and
1930's, and was a combined system until new storm sewers were
installed in the late 1950's. This contributes at times, to
excessive infiltration and inflow during snow melts, severe
rains and high lake levels. Step I studies are presently being
conducted to locate the problem areas of the system.
Maintenance of the collection system other than the lift
stations is performed by the Public Works Department.
PROBLEMS THAT DEVELOPED
During the first years of operation a few problems developed and
were solved by the operators. These included changes in alum
feed points, sampling equipment, digester piping, and sludge
handling. The problems as well as the solutions we employed are
explained below.
ALUM APPLICATION POINTS
It was found that during low flows the alum dosages needed to be
increased considerably to remove the required amounts. Also,
with low flows, concentrations of phosphorus increased, creating
the need for an increase in alum application.
Feed points at the secondary wet well did not provide enough
turbulance for proper mixing, so a temporary feed line was
installed to the sixth stage of each RBC path. This provided
enough dispersion for coagulation and flocculation, but after
104
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passing over a weir, through the wet well, and being pumped to
the secondary clarifier, the floe was broken up. By adding alum
to the primary wet well, dosages could be reduced at times, but
results were not consistent.
Temporary lines were installed in 1979 to the discharge side of
the primary pumps. A 30% reduction in the feed rate was found
to achieve the same results. Permanent feed lines were then
installed to each of the primary pumps. This has proven
effective during both low and high flows.
METHANE GAS UTILIZATION
The heating system of the building and the primary anaerobic
digester was designed to use both methane and natural gas.
Methane gas has a content of about 650 BTU per cubic foot, and
the boiler needed a rate of 5090 cubic feet per hour. The gas
pressure in the digester would raise a column of water 10 inches
(25.4 cm). A 2-inch (5.1 cm) gas pipe had been installed from
both digesters. The floating cover of the secondary digester
can hold about 4,000 cubic feet of gas. A sufficient gas rate
was not available to sustain the gas boiler, since the piping
extends some 70 feet (21.5 m), plus the meter, check valve,
flame arrester, and etc. By reducing the orifices of the
burner, some gas could be burned at times.
With the cleaning of the digesters in 1977, the portion of
2-inch (5.1 cm) pipe inside the secondary digester was changed
to 4-inch (10.2 cm) with the intent of changing all the piping
to this larger size.
105
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After temporarily connecting to clean the primary digester and
to burn off the gas, we found the boiler would operate at all
times. The remainder of the pipe has never been changed.
SLUDGE ODORS
Sludge, especially when controlling ammonia, must be removed at
intervals of 2 to 3 hours to eliminate bulking and its odors.
Sludge remaining at the bottom of the clarifiers will soon
become anaerobic and de-nitrify. Higher temperatures will also
accelerate bulking.
Secondary sludge must be removed manually. When the plant is
not manned on week-ends and holidays, we occasionally experience
rising sludge. An automatic sludge removal system would be
advantageous, as these clarifiers are uncovered and the odors
are readily noticed by our neighbors.
Combined sludges are pumped to the anaerobic digesters at two to
three hour intervals to assure proper utilization of digester
capacity and functions.
DIGESTER UPSET
In the six years of operations, only once were the digesters
upset. This happened in 1976, when gas production ceased and
the digesters went "sour". The nitrifiers on the RBC units were
disrupted as well.
The supernatant from the primary digester contained small
cellophane-type pieces of irregular shapes, somewhat resembling
bleached potato peelings. The volatile acid/alkalinity ratio
rose above 1.0 and the pH was dropping below 6.4.
106
-------
To correct the problem, heat was maintained at 90°F in the
digester and continuous mixing was was employed. About 300
pounds of soda ash were added over a 10-day period to hold the
pH near 7.0. Within two weeks the digesters were back
functioning normally.
The only explanation as to the cause of the upset was that the
city fire department floor had been stripped of several layers
of paint using paint remover which was flushed to the sanitary
sewers.
SAMPLING EQUIPMENT INADEQUACIES
The original sampling equipment supplied with the plant did not
provide representative samples. The three samples required were
raw wastewater, primary effluent, and final effluent. Only the
final effluent samples could be collected continuously.
The samplers had a small opening about the size of the lead in a
pencil, and the raw and primary effluent samples soon clogged
the orifice. The pumps for raw and primary effluent had 1
1/2-inch (3.8 cm) suction piping but only 1-inch (2.54 cm)
discharges. The primary effluent would pass easily enough,
however, the raw pump would plug at the 1-inch opening almost
immediately.
In 1975, a dipper type three-stage sampler with refrigeration
was purchased from "Sonford Products" of Minneapolis, Minnesota
and installed by the plant operators. All piping to the sampler
was increased to 1 1/2-inch (3.8 cm) with provisions provided
107
-------
for backflushing with final effluent. A submersible raw sample
pump was installed directly behind the bar screen. The pump
delivers 15 gallons per minute to the sampler and seldom causes
any problems. The new sampling system works well with very
little maintenance and we are assured of representative samples.
ENERGY AND CHEMICAL COSTS
The energy and chemical uses and costs associated with the plant
operation for 1978 are summarized in Table 6. The costs shown
per million gallons reflect actual prices Gladstone paid for the
respective commodities in 1978.
Electricity consumption is of primary interest and the table
shows electrical power consumption in terms of raw sewage
pumping, secondary (RBC) treatment, and anaerobic digestion.
The power consumption for the RBC units actually includes power
consumption by clarifier drives, intermediate pumps, lights,
ventilating equipment, etc., and computes to an average of
approximately 38 running horsepower at any given time. Of this,
approximately 80 percent (30 hp), including power draw by the
RBC units, could be considered independent of actual flows.
Based on measured power consumptions by the six RBC drive units
in 1975, the RBC system draws an average of 25-26 horsepower at
any given time.
TOTAL FACILITY BUDGET
Table 7 begins with the total facility budget and is followed by
f
some of the major operating expenses. The remainder of the
budget incorporates items such as the collection system, audit,
administration, engineering, insurances, and etc.
108
-------
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Table 7
1979 Fiscal Year Budget
Total Facility Budget $178,000.00
Power
Lift Stations 32,607 KWH
Plant 313,627 KWH
Total Power Costs 14,781.97
Natural Gas 1,185,490 cu ft 2,861,87
Chlorine 4,550 Ibs 827.25
Aluminum Sulfate 95,648 Ibs 4,497.96
Polymer 501 Ibs 1,005.52
Labor 7,136 man-hours 57,088.00
Plant Maintenance 3,000.00
Parts, Supplies, Miscellaneous 4,000.00
Equipment Rentals 3,000.00
110
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REVENUE TO OPERATE
In 1972, water meters were installed in every home. The water
plant staff maintains these meters. All meters larger than
1-inch are checked at three year intervals. Small household
meters are checked to assure accuracy as needed. Ten percent of
the meters have registered 1 million gallons since 1972 and a
routine maintenance program is being initiated.
The water distribution system originally began in 1889 and at
the present, approximately 72% of the water produced can be
accounted for.. 63% of the water treated at the wastewater plant
comes from inflow and infiltration.
Prior to 1969, no wastewater charges were collected, with the
system operating solely on taxes. Water charges prior to 1970
averaged $1.00 per month. Today, with the new water filtration
plant and the upgraded wastewater facility, the average house-
hold using 5,000 gallons of water pays $11.65 for water and
$10.49 for wastewater per month.
i
SUMMARY
We believe the RBC treatment system is an ideal treatment
process for the city of Gladstone, Michigan. Excellent
treatment results are being obtained and plant effluent quality
is well within design limits. Consistent nitrification at
loading below 2 gpd/sq ft is being achieved as an added bonus
toward high quality treatment.
Ill
-------
The system has been very consistent in achieving wastewater
treatment and permitting stable solids handling procedures. Few
problems have occurred with the day-to-day operation of our RBC
secondary treatment system.
ACKNOWLEDGEMENTS
The author wishes to thank Williams & Works of Grand Rapids,
Michigan for their cooperation in the preparation of this paper.
112
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CONTROL TECHNOLOGY FOR NUTRIENTS IN
MUNICIPAL WASTEWATER TREATMENT IN SWEDEN
Bengt G. Hultman
Research Engineer
Swedish Water and Waste Water Works Association
Regeringsgatan 86
S-lll 39 STOCKHOLM
Sweden
NEED FOR NUTRIENTS CONTROL
Sweden is comparatively rich in lakes with more than 20,000 ex-
ceeding 0.1 sq. km in area. Most of them are fairly shallow. In
their natural states the lakes and coastal areas are deficient in
nutrients. This means that the lakes and coastal areas will react
to artificial supply of nutrients from for instance urban areas.
At the end of the 1950~s limnologists began to warn about the
deterioration of the water quality in lakes and coastal areas
due to the increased rate of the growth of algae and other vege-
tation. Rodhe (1958) pointed out that the phosphorus in sewage
could increase the productivity in natural waters as much as com-
mersial fertilisers applied on land. Different investigations on
lakes indicated a significant rise in the water's content of
phosphorus and biomass.
During two weeks in August 19-72 an extensive lake survey was car-
ried out by the National Swedish Environment Protection Board and
the County Administrations (Johansson and Karlgren, 1974). A to-
tal of 1250 minor and medium-sized lakes were examined. Although
not being the primary aim of the study, an attempt was made to
estimate the degree of nutritional influence on the lakes resul-
113
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ting from human activities. It was found that the inorganic phos-
phate content in water showed similar regional variations as that
of total phosphorus and of total nitrogen with low concentrations
in the low-productive lakes in northern Sweden and parts of south-
ern Sweden and high concentrations in the high-productive lakes
of the plains.
Based on the lake survey and complementary studies Hannerz and
Forsberg (1975) estimated that less than 10 % of the Swedish la-
kes were eutrophic. In south Sweden about 10 to 20 % of the lakes
were eutrophic and the percentage of eutrophic lakes in the Stock-
holm county amounted to about 50 %.
Several substances such as phosphorus, nitrogen, carbon dioxide,
iron and vitamins can stimulate algal growth. Of these substances
only phosphorus and nitrogen have been considered as main factors
for stimulating eutrophication. A strong emphasis has been laid
on phosphorus removal as the method for control of eutrophication
especially from the National Swedish Environment Protection Board,
while nitrogen has been considered to be of minor importance. The
reasons for this view seem to be:
Phosphorus seems to be rate limiting for algal growth
in most Swedish lakes based on values of the weight pro-
portion of nitrogen to phosphorus, which is about 25:1
for natural or low polluted lakes. '
A large fraction of phosphorus comes from point sources
which may be more easily controlled than diffusive sour-
ces.
- Algae have the possibility of taking up nitrogen from the
atmosphere if nitrogen is a limiting growth factor.
114
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In the end of the 1960's phosphorus removal was a much
more wellknown technique than nitrogen removal in Sweden.
For a total of about 900 samples from surface water from 20 waste
affected lakes in Sweden during August-October 1972 Forsberg et
al. (1975) found phosphorus to be the growth limiting nutrient
in waters having total-P values less than 0.05 mg/1. Above 0.1
mg P/l nitrogen played the principal role. Between these values
the growth was primarily limited by phosphorus or nitrogen or
chelating agents.
Nitrogen seems to be the primarily rate limiting factor for algal
growth in case of eutrophic lakes (Forsberg, 1977) and in some
coastal waters as the Stockholm archipelago (Lindahl and Melin,
1973). In this case the policy of the National Swedish Environ-
ment Protection Board has been to try to reduce the phosphorus
supply to the water body as much as possible in order to make
phosphorus the growth limiting substance (Anonymous, 1971).
IMPLEMENTATION OF NUTRIENTS CONTROL
LEGISLATION AND ADMINISTRATION
Legislation concerning discharge of waste water into lakes and
rivers has been in existence in Sweden since the end of the
1930's. A new law, the Environment Protection Act, came into for-
ce in July 1969 and tightened up regulations considerably.
The Environment Protection Act applies to what are termed pollu-
ting activities, i.e. the discharge of effluent, solids or gas
115
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from land, a building or an installation or the use of such pro-
perty in a manner liable to cause water pollution, atmospheric
pollution, noise, vibration, the emission of light etc., if the
nuisance thus caused is more than temporary (National Swedish
Environment Protection Board, 1979a).
The chief principle of the act is to prevent environmental dis-
turbances as far as possible. The precautionary measures, such
as effective methods of wastewater treatment, shall be "economi-
cally feasible" and "technically practible".
Sewage from locations with more than 200 inhabitants must not be
emitted without a permit. A special board, the Franchise Board
for Protection of the Environment, holds the responsibility for
the granting of permits. The obligation to apply for a permit is
however not compulsory. The National Swedish Environment Protection
Board may after due examination exempt an applicant from the need
to apply to the Franchise Board for a permit. In exemption cases,
the Board attempts through negotiations to come to an agreement
with the applicant as to the conditions to be applied to the ac-
tivity. An exemption granted lacks formal legal validity - as
opposed to a permit - and may be withdrawn (National Swedish En-
vironment Protection Board, 1979a).
SOURCE CONTROL
The synthetic detergents which were introduced in Sweden during
the 1950"s have greatly improved laundry cleaning efficiency. Po-
lyphosphates were totally dominating as complexing agents in the
116
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detergents. In the end of the 1960"s the average phosphate con-
centration was about 35 % in cleaning agents and in some special
products the phosphate concentration could amount to more than
60 % (Kjellman, 1975).
In the middle of the 1960"s municipal sewage from urban areas
contained phosphorus corresponding to about 4 g P per person and
day. Approximately half of this amount originated from detergents
(Ahl et al., 1967). The general opinion that phosphorus was the
main agent causing eutrophication lead to investigations of dif-
ferent methods to reduce the phosphate concentration in detergents.
In order to comply with authorities different manufacturers dimi-
nished the amount of phosphates in their detergents. As can be
seen from Table 1 the use of phosphate in detergents diminished
from about 3.9«106 kg in year 1968 to about 2.65»106 kg in 1972,
corresponding to a decrease of 32 %. Due to the decrease of phos-
phate in detergents the phosphorus content in sewage diminished
to about 3.3 g P per person and day of which about 30 % originated
from detergents (Kjellman, 1975). The use of phosphorus in deter-
gents has increased a little after 1972.
The trisodium salt of NTA may be used as a partial substitute for
or a complement to sodium tripolyphosphate as builder in house-
hold detergents. NTA was introduced on the market at the end of
the 1960"s (see Table 1). Several studies were performed in order
to evaluate the biodegradability of NTA (Forsberg and Lindquist,
1967, Bouveng et al., 1968 and 1970, and Bjorndal et al., 1972).
117
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The results obtained showed that aerobic biological processes
are capable of degrading NTA fairly efficient under normal con-
ditions of operation. However, different foreign reports, for
instance the Epstein report, raised some doubts that NTA could
be safely used without negative consequences on the environment.
These doubts lead to a decreased interest in using NTA in deter-
gents (National Swedish Environment Protection Board, 1970) and
the use of NTA in detergents has decreased during the 1970~s.
CHOICE OF PROCESS TECHNOLOGY FOR NUTRIENTS CONTROL
The first sewage works with chemical precipitation was built in
1961 in Aker, a small municipality with about 2,000 persons con-
nected to the sewage works. The treatment plant was equipped for
primary sedimentation with subsequent chemical precipitation whe-
re the floes were separated in a flotation unit. The chemical
precipitation agent was aluminium sulphate.
The sewage works in Aker was built before any significant research
had started in chemical precipitation. In the middle of the 1960"s
several research projects started on combined biological and che-
mical treatment of sewage. At that time the two processes which
were considered were simultaneous precipitation and post-precipi-
tation. Studies were performed in a laboratory scale, pilot plant
scale and as full scale experiments.
Early studies on the simultaneous precipitation process gave rat-
her high effluent values of total phosphorus. Pilot plant studies
with simultaneous precipitation with aluminium sulphate gave eff-
118
-------
luent values of total phosphorus of about 2 mg P/l (Balm§r et
al., 1968). Full scale tests at Eolshalls sewage works in Stock-
holm during a short test period showed effluent values of total
phosphorus of about 1-1.5 mg P/l. Addition of aluminium sulphate
caused a lower reduction of the BOD-values due to separation
problems in the final sedimentation basin (Cronholm, 1968). Ulm-
gren (1969) reports other full scale tests in which simultaneous
precipitation were studied giving high effluent values of total
phosphorus. Laboratory studies of the simultaneous precipitation
process, however, showed that it was possible to reach effluent
values of total phosphorus below 1 mg P/l (Ericsson, 1967).
Laboratory experiments with post-precipitation showed that an
effluent value could be reached of total phosphorus below 1 mg P/l
(Ericsson, 1967, and Weijman-Hane, 1968). Similar results were
obtained in evaluation of the first built sewage works with post-
precipitation (National Swedish Environment Protection Board,
1969) .
Based on the rather few experimental studies performed in Sweden
concerning chemical precipitation and foreign experiences for
instance in Switzerland the National Swedish Environment Protec-
tion Board strongly recommended post-precipitation instead of si-
multaneous precipitation as the removal method of phosphorus. In
1968 the expansion period began with chemical treatment plants
with the purpose of reducing as much as possible of the phospho-
rus content in wastewaters.
119
-------
No significant interest was laid on nitrogen removal. However,
some research started in the middle of the 1960"s concerning
nitrogen removal, especially by use of biological methods
(Hultman, 1973, and Ericsson, 1975).
DESIGN GUIDELINES
To guide those who prepare or scrutinize proposals for treatment
plants the National Swedish Environment Protection Board (1971)
prepared "Guidelines for design of sewage treatment plants". In
the guidelines the following are given: design values for sludge
loads on the activated sludge process, BOD loads on trickling
filters, detention time in flocculating units, surface loads in
sedimentation basins etc (Ulmgren, 1975a).
EMISSION CONTROL
Instructions for emission control in Sweden have been issued by
the National Swedish Environment Protection Board (1973). The
sampling frequency in relation to the required parameters total
BODj, total COD and total phosphorus is given in Table 2. In ad-
dition local authorities may demand more extensive emission cont-
rol and programs for recipient control.
STATE GRANTS
State grants are since 1st of July 1968 payable on certain con-
ditions for the construction, enlargement or alteration of sewage
purification plants, outfalls and, in some cases, intercepting
mains as well (National Swedish Environment Protection Board,
1968) .
120
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TABLE 1. YEARLY CONSUMPTION OF RAW MATERIALS FOR WASHING,
DISH-WASHING AND OTHER CLEANING MATERIALS USED IN
HOUSEHOLDS IN SWEDEN 1968-1972 (The consumption
figures are given in thousand kilograms; 1 kg =
2.205 Ib) (Kjallman, 1965).
Raw material
Year
1968 1969 1970 1971 1972
Soap
Synthetic tensides
Phosphates
NTA
Other organic com-
plexing agents
1377
7500
3920
111
116
2037
7704
3644
1019
115
2624
7450
2855
1711
226
2597
7443
2797
1525
330
2766
8483
2650
1373
492
TABLE 2. FREQUENCY OF SAMPLING IN EMISSION CONTROL
(National Swedish Environment Protection Board/ 1970)
Parameter
Person
equivalents (p.e.) connected to treatment plant
200-2000 2000-5000
COD(a)
BOD20000
4 /month
I/month
4 /month
121
-------
Grants are gauged according to degree of purification and are
payable at rates between 30 and 50 per cent of approved con-
struction costs (see Table 3). During the fiscal years 1971/72-
1973/74 grants were payable 25 per cent in excess of those rates
given in Table 3. This formed a part of a programme to create
jobs (National Swedish Environment Protection Board, 1979a).
Grants given for different types of treatment are exemplified
in Table 4 based on rates in Table 3.
PRESENT SITUATION
The general policies for implementation of the Environment Pro-
tection Act on sewage treatment as developed in the end of the
1960*s has essentially been maintained. Thus, a combined biologi-
cal and chemical treatment of municipal wastewater is normally
prescribed. In certain relatively few cases, only biological or
only chemical treatment may be allowed. In localities with poor
recipient conditions in relation to the discharge complementary
treatment (mainly post-filtration) is prescribed in addition to
biological and chemical treatment. Recently, requirements of nit-
rification has been prescribed for a sewage works in the Stock-
holm area. The main reason for this requirement is to diminish
the oxygen demand of the wastewater which may give rise to oxygen
deficit at the bottom of certain parts of the Stockholm archipe-
lago and thereby cause leakage of phosphorus from the bottom se-
diments. Thus, the requirement of nitrification is to prevent
phosphorus leakage and thereby according to the general view
decrease algal growth.
122
-------
TABLE 3. STATE GRANTS FOR MUNICIPAL WASTEWATER WORKS
(National Swedish Environment Protection Board, 1968)
Percentage BOD-, pu- Percentage phosphorus purifica-
rification effect tion effect
<50 50-89 >90
Percentage grant:
60-74 30 35 40
75-89 30 35 45
>90 35 40 50
TABLE 4. PERCENTAGE GRANTS FOR DIFFERENT PROCESS COMBINATIONS
(National Swedish Environment Protection Board, 1969)
Process combination Percentage grant
Simultaneous precipitation 35
Direct precipitation 40
Post-precipitation 45-50
123
-------
Sewage purification facilities in Sweden have expanded very
quickly during the last decade (see Figure 1). In the beginning
of 1979 about 640 municipal wastewater treatment plants were ope-
rated with combined biological and chemical treatment correspon-
ding to about 72 % of the total amount of wastewater from urban
areas.
The dominating process combination is post-precipitation with a
share of more than 80 % calculated on the number of treatment
plants with chemical precipitation (see Table 5). However, some
of the largest sewage works, for instance in the Stockholm region,
use pre-precipitation or simultaneous precipitation.
Aluminium sulphate has been the dominating precipitation agent.
During the last years especially larger sewage works have changed
to iron salts (see Table 6). This depends on that the production
of ferric chloride from waste products has considerably lowered
the price of the chemical. Besides there are some benificial ef-
fects on the sludge properties in the use of iron salts compared
with aluminium sulphate.
EVALUATION OF NUTRIENTS CONTROL MEASURES
OPERATIONAL RESULTS
Several papers have been written on experiences of full scale
operations of chemical precipitation in Sweden (Eklund, 1974,
Gronqvist et al., 1978, Hultman, 1978, Isgard and Ericsson, 1976,
and 1978, and Ulmgren, 1975a and 1975b). These papers discuss
124
-------
Percent of the population in urban areas(localities)
1979-01-01
100
1970
1975
Chemical
treatment
Biological-
71%| chemical
treatment
Complementary
1,5%J treatment
(filtration etc.)
1980
Type of sewage treatment
Number of
treatment plants
Number of persons
served
No treatment
Sedimentation
Biological treatment
Chemical treatment
Bio. chemical treatment
Complementary treatment
156 (-34)
380 (-37)
141 (+ 3)
625 (+18)
18 (+ 2)
7 000 (- 1 000)
181 000 (- 21 000)
1 398000 (-110000)
324000 (+ 22000)
4833000 (+ 106000)
107000 (+ 7000)
1 320 (-48)
The figures in brackets refer to the change since January 1 st, 1978
6 850 000
Figure 1. Sewage Treatment in Sweden 1965-1979
125
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TABLE 5. DIFFERENT TYPES OF SEWAGE WORKS WITH CHEMICAL PRECIPI-
TATION IN SWEDEN IN THE BEGINNING OF 1978
(National Swedish Environment Protection Board, 1979b)
PROCESS COMBINATION:
Direct precipitation
Pre-precipitation
Simultaneous precipitation
Post-precipitation
NUMBER OF PLANTS
138
17
35
554
Post-precipitation systems;
Trickling filters
Activated sludge
Separation of chemical floes
by contact filtration
Polishing by deep-bed filters
49
505
11
16
TABLE 6. USE OF DIFFERENT PRECIPITATION AGENTS AT MUNICIPAL SE-
WAGE WORKS IN SWEDEN IN THE BEGINNING OF 1977 AND 1979
(National Swedish Environment Protection Board, 1979b)
TYPE OF CHEMICAL PRECIPITATION AGENT:
Number of
plants
Aluminium
sulphate
600 (578)
Ferric & Lime
ferrous
iron
92 (60) 60 (48)
Iron
salts &
lime
26 (22)
Aluminium
sulphate &
iron salts
4 (3)
Percentage of
connected po-
pulation 49 (69) 42 (23) 5 (3) 2 (3) 2 (2)
Numbers from the beginning of 1977 are within brackets,
126
-------
different process configurations, the influence of different ope-
rational parameters such as dosage, pH-value in the flocculation
step and type of chemical precipitation agent and the influence
of separation methods.
Data from the emission control at municipal sewage works shall be
sent to the National Swedish Environment Protection Board once a
year. Compilations of such data have been published by the Natio-
nal Swedish Environment Protection Board (1977 and 1979b). Obtai-
ned results for different treatment systems are shown in Table 7.
The results are compared in the table with expected results from
treatment plants with a good operation and no significant distur-
bances based on results reported by Gronqvist et al. (1978).
A large fraction of the Swedish municipal sewage works do not
operate reliably. Investigations of post-precipitation plants in-
dicate that effluent values of BOD- are not below 15 mg/1 (requi-
red limit) for about 30 % of the plants and effluent values of
total phosphorus are not below 0.5 mg P/l (required limit) for
about 40 % of the plants (National Swedish Environment Protection
Board, 1977).
Full scale experiences of simultaneous precipitation plants in
the Nordic countries have been put together by Gronqvist and
Arvin (1979). It was shown that much better results could be ob-
tained for the treatment plants than results shown in Table 7.
The average concentration of total phosphorus from five simulta-
neous precipitation plants in the Stockholm area was 0.6 mg P/l.
127
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TABLE 7. OPERATIONAL RESULTS BY USE OF DIFFERENT CHEMICAL PRECI-
PITATION METHODS
PROCESS COMBINATION
Direct precipitation
Pre-precipitation
Simultaneous preci-
pitation
Post-precipitation
OPERATIONAL RESULTS
IN 1977
ROD
±J\-/ LJ n
mg/1
39
35
28
10
(1)
tot
mg/1
0.70
0.98
1.48
0.53
EXPECTED RESULTS
FOR PLANTS WITH NO
SIGNIFICANT
BANCES (2)
Ptot' mg
-
0.5-0.
0.5-0.
0.5-1.
DISTUR-
/l
8
8
2 (3)
Post-precipitation
followed by deep-
bed filtration
0.22
0.2-0.4 (4)
0.15-0.3 (5)
Notes: (1) Average values from different plants. Data from
National Swedish Environment Protection Board (1979b)
(2) According to Gronquist et al. (1978).
(3) Post-precipitation with aluminium sulphate at pH
6.5-7.2 or lime in single stage at normal loaded
plants.
(4) Post-precipitation with aluminium sulphate at pH
5.5-6.4, with ferric chloride and recirculation of
sludge to the aeration basin or with lime in single
stage at low loaded plants.
(5) Post-precipitation with aluminium sulphate at pH
5.5-6.4.
128
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In order to elucidate the reasons of the unsatisfactory removal
efficiencies of certain sewage works an enquiry was sent in spring
1979 to the County Councils. These were requested to give their
opinion of the reasons for the unsatisfactory results of sewage
works with effluent values of BOD_ and total phosphorus above 15
mg/1 and 0.5 mg P/l, respectively. Several explanations were gi-
ven such as hydraulic problems, difficult industrial wastes and
unreliable machinery equipment. The percentage distribution of
reasons to unsatisfactory results is given in Table 8.
COSTS OF POST-PRECIPITATION PLANTS
The costs for post-precipitation plants based on average values
from different Swedish reports are put together in Table 9. The
capital costs are somewhat higher than the operating costs. Due
to increasing treatment costs for diminishing sizes of the sewage
works there is a tendency to centralize the wastewater treatment.
The grant system has promoted this development. The use of comple-
mentary treatment by deep-bed filtration will increase the total
costs for a post-precipitation plant 15-20 %. Different cost
factors for the operating costs are shown in Table 10.
EFFECTS ON RECIPIENTS
In order to elucidate the effects of biological and chemical
treatment on the water quality in the recipient the National Swe-
dish Environment Protection Board started a program in 1972 for
analyzing the conditions in a number of different recipient lakes
(Forsberg et al., 1975).
129
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TABLE 8. CAUSES OF UNSATISFACTORY REMOVAL EFFICIENCIES OF POST-
PRECIPITATION PLANTS (Carlsson and Nordstrom, 1979)
CAUSE
Hydraulic problems
Industrial wastes
Machinary equipment
Process technology
Maintenance
Repairs, reconstruction
Unreliable analysis (1)
Unknown causes
PERCENTAGE DISTRIBUTION, %
18
12
19
17
2
4
17
12
Note: (1) Probably depending on significant nitrification in
BOD-bottles during the BOD7~measurement.
130
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TABLE 9. APPROXIMATE COSTS FOR SEWAGE TREATMENT (1978).
Number of per-
son equivalents
(p.e.)
Costs for post-preci-
pitation plants (inclu-
ding sludge treatment)
Capital
costs
Skr
p.e.-year
Operating
costs
Skr
p.e.-year
Additional costs
for deep-bed filt-
ration
Capital Operating
costs costs
Skr Skr
p.e.-year p.e.«year
2,000
5,000
20,000
50,000
130
100
60
45
100
70
50
40
—
25
10
7
—
8
4
3
Notes: 1 Skr = 0.24 US dollars
In calculation of capital costs the annuity used is 10 %
and 13 % for post-precipitation plants and deep-bed fil-
ters, respectively.
Average municipal water consumption is about 400 1 per
person and day in Sweden.
TABLE 10. OPERATING COSTS FOR POST-PRECIPITATION PLANTS (INCLU-
DING SLUDGE TREATMENT) (1978)
COST FACTOR
Labour and administration
Chemicals
For chemical precipitation
For sludge conditioning
Energy
Sludge transportation
Other costs factors
PERCENTAL COSTS, %
30
25
(15)
(10)
20
10
15
Too
131
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From the experiences of phosphorus removal positive responses
have been reported from some water bodies. In other lakes delayed
recovery has been observed after nutrient reduction. In some la-
kes, where the phosphorus load was reduced by 30-40 %, no marked
improvements were noted. The results available indicate that a
comparatively great change in phosphorus load must occur in or-
der to get significant improvement in water clarity in the lakes.
As the phosphorus load from treatment plants is often the domi-
nant phosphorus source, reduction of phosphorus by advanced treat-
ment seems to be a good tool for controlling eutrophication in
many lakes (Ryding, 1978a and 1978b).
TRENDS IN IMPROVEMENT OF CONTROL OF NUTRIENTS
The operating costs have steadily increased at Swedish sewage
works. Therefore great interest has been directed towards biolo-
gical-chemical treatment methods which can reduce the operating
costs and which are more efficient. Such methods include the use
of counterflow of precipitated sludges, two-step precipitation,
regulation of the alkalinity and automatic control.
For a constant value of the suspended solids in the effluent it
is advantageous to have a low fraction of phosphorus in the sus-
pended solids in order to obtain low effluent values of phospho-
rus. If the effluent concentration of suspended solids is 10 mg/1
and the fraction of phosphorus in the suspended solids 6 % and 2
% the effluent concentration of suspended phosphorus will be 0.6
and 0.2 mg P/l, respectively.
132
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A suitable way to diminish the fraction of phosphorus in the sus-
pended solids is to decrease the influent phosphorus concentration
before the precipitation step. This technique has been tried in
full scale at several sewage works in Sweden. Different examples
are:
Two-step precipitation at Balinge sewage works (Holm-
strom, 1977) by use of the combination of simultaneous
precipitation and contact filtration in which process
combination the principal part of phosphorus removal
occurs in the simultaneous precipitation step after
which still more phosphorus is removed by the addition
of low concentrations of ferric iron before a deep-bed
filter.
Two-step precipitation at Kappala (Isgard and Ericsson,
1978) and Bankeryd sewage works in which simultaneous
precipitation is followed by post-precipitation.
Recirculation of post-precipitated sludge to the aera-
tion basin of the activated sludge process (Gronqvist
et al., 1978). The phosphorus reduction in the biologi-
cal step is hereby improved and the phosphorus concent-
ration before the post-precipitation step will be much
lower than if no recirculation takes place. Some preli-
minary results indicate, however, that nitrification
may be inhibited by recirculation of aluminium contai-
ning post-precipitated sludges.
Use of biological phosphorus reduction at Kristianstad
sewage works by use of an anaerobic zone in the first
part of the aeration basin. In this way the phosphorus
concentration is diminished before the post-precipita-
tion step.
These operational modifications of an existing post-precipitation
plant have shown very promising results including better removal
efficiencies of total phosphorus, lower total amount of chemical
precipitation agents and better sludge properties. It therefore
seems probable that a large fraction of the Swedish post-precipi-
tation plants will change to a modified operating scheme.
133
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The alkalinity of the effluent from a biological step is mainly
determined by the influent alkalinity and the degree of nitrifi-
cation and denitrification. In nitrification the produced amount
of hydrogen ions reduces the alkalinity of the wastewater. This
reduction often leads to reduced requirements of aluminium sulp-
hate or lime in post-precipitation and several treatment plants
are operated in this way in Sweden (Ericsson et al., 1976, and
Gronqvist et al., 1978). Promising results have been shown by
regulation of the alkalinity of the effluent from an activated
sludge process by regulation of the degree of nitrification and
denitrification by the supply of oxygen (Olsson, 1980) .
SUMMARY
During the 1950's observations were made and the conclusion drawn
that the water quality in some lakes and coastal waters had dete-
rioted. Different recipient studies indicated that phosphorus was
the main factor which caused this deterioration. Some efforts were
made to decrease the phosphate concentrations in the synthetic de-
tergents and approximately a 30 % reduction of the phosphate
amount in synthetic detergents was obtained between 1968 and 1972.
In 1968 the expansion period began with chemical treatment plants
and in the beginning of 1979 about 640 municipal wastewater treat-
ment plants were operated with combined biological and chemical
treatment corresponding to about 72 % of the total amount of
wastewater from urban areas. At present a large interest has been
directed towards modified operating schemes in order to get bet-
ter removal efficiencies and savings in operating costs.
134
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narsaltreduktion. Vatten, 25, 2, pp 140-145 (in Swedish).
137
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Ulmgren, L. (1975a): Experiences and results from chemical pre-
cipitation of domestic waste water in full-scale
plants. Prog. Wat. Tech., Vol 7, Nos 3/4, pp 409-416.
Ulmgren, L. (1975b): Swedish experiences in chemical treatment
of wastewater. J. Water Pollution Control Federation,
47, 4, pp 696-703.
Weijman-Hane, G. (1968): Narsaltreduktion. Vatten, 24, 2, pp 106-
111 (in Swedish).
138
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ECONOMICAL AND EFFICIENT PHOSPHORUS CONTROL
AT A DOMESTIC-INDUSTRIAL WASTEWATER PLANT
Doris Van Dam
Wastewater Treatment Plant Superintendent
Grand Haven - Spring Lake, Michigan Sewer Authority
INTRODUCTION
In 1968/ the Michigan Water Resources Commission (MWRC) issued
orders for phosphorus and other pollutant reductions to commun-
ities and industries whose wastes were being discharged to the
waters or tributaries of the Great Lakes by December 1972. The
MWRC adopted its standard from the Federal State Conference on
the pollution of Lake Michigan and its tributary basin held in
Chicago, Illinois in March 1968.
The response at Grand Haven and Spring Lake, Michigan, located
on the sandy coast where the Grand River enters Lake Michigan,
was to form a combined sewer authority and build a new central
treatment plant. The plant was designed not only to process
domestic wastes, but also to receive a substantial contribution
from the Eagle Ottawa Leather Co., a chrome and vegetable tan-
ner of 12,000 hides per week and a principal employer in the
Grand Haven - Spring Lake area. (Figure 1).
It is the purpose of this paper to discuss the special challen-
ges the merged waste flow posed to design and subsequent opera-
tion of the treatment plant. How concentrated side streams,
such as heat treatment supernatants, must be considered in over-
all plant efficiency is discussed. The techniques used to control
139
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phosphorus at a very low cost are presented. A summary of sev-
eral years of plant efficiency and cost figures accompany the text.
BACKGROUND
The MWRC requirements called for an 80 percent removal of phos-
phorus for Grand Haven, Spring Lake, and the Eagle Ottawa Leather
Co., as well as combined maximums from all three sources of 1,126
pounds per day (511.2 kg) of BOD, and 30 mg/1 of suspended solids.
At the time, Grand Haven, population 10,500, was served by an out-
dated primary treatment plant, Spring Lake, population 3,034, em-
ployed an overloaded Imhoff tank, and Eagle Ottawa Tannery efflu-
ent was simply screened before discharge to the Grand River.
To meet the requirements, the newly-formed joint district construct-
ed a single 5.0 mgd (18,925 cu m/day) activated sludge plant. The
plant went on line in November, 1973, and 1978-1979 average con-
tributions from the three sources were 2.1 mgd (7,759 cu m/day)
from Grand Haven, 0.4 mgd (1,476 cu m/day) from Spring Lake, and
0.8 mgd (3,179 cu m/day) from Eagle Ottawa (Figure 2 ).
Although tannery wastes have amounted to just 26 percent of treat-
ment plant flow, they represent 81 percent of total influent BOD,
and 80 percent of influent suspended solids. The tannery waste
contains in mg/1 60 sulfides, 34 chromium, 57 ammonia, 2911 CODf
and a total nitrogen as N of 106 (Figure 2 ).
The treatment plant employs grit removal, phosphorus removal, pri-
mary clarification, activated sludge and chlorine contact; solids
are conditioned thermally prior to vacuum filtration (Figures).
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All domestic flow is comminuted prior to reaching the grit tank.
Eagle Ottawa wastes are screened at the tannery. Grit collected
on the bottom of a square, aerated-type grit collector is removed
by means of an air lift pump from the hoppered end of the tank.
Grit is washed by means of a mechanical inclined screw mechanism.
Ferrous sulfate for phosphorus removal is added to the total flow
in the rapid mix tank located in the grit building.
Air flocculcation is provided in the primary clarifiers for poly-
mer flocculation.
The plant includes three 60-foot (18.29 m) diameter, primary clari-
fiers, 200,000 gallon (757 cu m) capacity each. The three aeration
tanks have a total capacity of 1,700,000 gallons (6,434.5 cu m), and
and are equipped with duo-spargers and coarse bubble diffusion.
The aeration tanks are arranged so that the activated sludge pro-
cess can be operated in one of four modes: conventional, complete
mix, step aeration, or contact stabilization. Air is provided by
four centrifugal blowers, each having a capacity of 5,200 cubic
feet (145.6 cu m) per minute.
The three final clarifiers are the same size as the primaries, and
are equipped with suction-type sludge removal mechanisms. The chlo-
rine contact tank has been constructed to provide two separated tanks
with gates so that either tank may be isolated for cleaning.
Effluent water is used for lawn sprinkling, the incinerator scrubber,
filter belt wash, foam suppression, line flushing, thickener, and
chlorinators.
144
-------
Return sludge pumps are 20 hp (14.914 kw) , and can provide 100
percent return sludge capacity. Sludge from primary clarifiers
is drawn off from a sump at the center of the clarifier by means
of positive displacement pumps, and pumped directly to two 45-
foot (13.716 m) diameter, 20-foot (6.096 m) deep covered thicken-
ing tanks, with total capacity of 1,000,000 gallons (3,785 cu m) ,
or 28,000 pounds (12,712 kg) per day of solids.
After thickening, sludge is processed through a wet oxidation unit
where it is thermally conditioned at a rate of 68 gallons (257.38
liters) per minute. Sludge is first ground in one of two grinders
which are piped in parallel to insure operation if one is out of
service.
Air is supplied by a 50 hp (37.29 kw), 134 scfm (3.75 cu m/min)
§ 500 spig (35.15 kg/sq cm) compressor, and the sludge-air mix-
ture is pumped to reactor pressure of 306 psig (21.51 kg/sq cm) by
a high pressure positive displacement ram-type pump. The material
is fed through stainless steel heat exchangers to a stainless steel-
clad reactor. A steam boiler maintains reactor temperature at 385°F
(195.9°C). A standby boiler, and a second high pressure pump, pro-
vide backup capability.
Oxidized sludge is decanted in a separate tank and dewatered on
one of two cloth-covered, 370 square foot (34.37 sq m) vacuum fil-
ters. When the incinerator is bypassed, sludge cake is hauled to
landfill or used on agricultural land.
Plant performance has averaged 96 percent BOD removal, 76 percent
COD removal, 96 percent suspended solids reduction, 88 percent
145
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phosphorus removal, and chromium reduction of 96 percent (Figure 4 )
SPECIAL PROBLEMS - LOCATION/ODORS
Inclusion of tannery wastes in the new treatment plant created con-
ditions which required special consideration from the very first.
Because the hair, lime and grease in tannery wastes tend to clog
sewer lines unless there is adequate sewer dilution or primary
treatment prior to discharge into sewers, plant siting became a
crucial decision. To minimize the anticipated difficulties in
moving tannery effluent over longer distances, the new treatment
plant was situated within the city limits of Grand Haven, immed-
iately sputh of the Eagle Ottawa plant. The location is in a semi-
residential neighborhood, and special provisions for odor control
have had to be implemented.
In the original scheme, all usual odor-producing areas (grit and
screening building, decant tank, thickeners, vacuum filters) were
covered. The areas are vented and odors drawn off to the inlet
of the aeration blowers and solubilized in the mixed liquor.
Because of equipment failures and the tannery contribution, how-
ever, odor problems unforeseen originally have required extraord-
inary odor control techniques.
TREATABILITY
Treatability of the tannery-domestic waste mixture was a second
important question. Pilot studies verified the effectiveness of
the activated sludge method, provided the chromium content of pri-
mary effluent could be reduced to approximately 5 mg/1 to avoid
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toxicity in the biological phase. This was achieved by blending
lime from the tannery's beamhouse to aid in the precipitation of
chromium hydroxide. The addition of sodium hydroxide to the tan-
nery waste prior to its combination with the domestic flow is also
possible. This has rarely been necessary, however, except for a
period during a strike when the tannery was operating with limited
staff and not using the beamhouse to full capacity.
Since the tannery wastes are discharged on a batch basis, with pH
ranging from 3 to 12, an equalization tank was incorporated into
the system to hold tannery efflyent and create an acceptable pH
level of 8.5 to 9.0.
In addition, the system is designed so that all tannery wastes
can be taken into one primary tank, exclusive of domestic wastes,
and treated separately, should that become necessary.
SIDESTREAM RECYCLE
A great deal has been said about the supernatant decant liquor
which is returned from thermally conditioned sludge to the treat-
ment plant. Sidestream treatment should be studied in light of
purpose and design of the total solids handling system and the
fate of solids throughout.
Let us deal with solids first. While thermal conditioning is high-
ly successful in making the difficult-to dewater sludge easily de-
waterable, it also solubilizes a portion of the raw suspended sol-
ids. At the same time, a relatively small amount, approximately 5
percent, of oxidation of volatile solids occurs, due to the addi-
tion of air in the thermal conditioning system.
148
-------
Supernatant recycle, of course, is another concern. After condi-
tioning, the oxidized sludge flow enters the decant tank, where it
thickens before it is sent to the vacuum filter for dewatering.
The decant supernatant, a relatively clear liquid resulting from
the thickening process, is decanted and returned to the aeration
tanks for treatment. While its suspended solids concentration is
only, 2460 mg/1, its COD, 8005, and P concentrations are 22, 320
mg/1, 9370 mg/1 and 45 mg/1 respectively, due to the solubilized
dissolved volatile solids. It constitutes the major biological
solids handling sidestream load on the plant. It also has some
phosphorus load. Additional capacity and operational flexibility
were designed into our secondary system to allow for adequate
treatment of the solids handling recycle streams.
PHOSPHOROUS REMOVAL
A chemical mixing, feeding and distribution system was provided to
provide chemical removal of phosphorous in the wastewater stream.
It was planned that the chemicals used for phosphorous removal
would include ferric chloride and polymer.
Ferric chloride would be delivered by truck and transferred to two
10,000 gallon (37,850 1) storage tanks located adjacent to the chem-
ical feed room underground outside the control building.
Because the concentrations of ferric chloride delivered to the
plant would vary from 38 percent to 45 percent during winter and
summer months respectively, the operator had flexibility as to how
to store and feed the ferric chloride. A dilution system was in-
stalled so that a constant dilution could be fed throughout the
149
-------
year if desired. Non-potable water could be added to the storage
tank along with air mixing from the bubbler system to provide the
desired diluted concentration. Should the operator not desire to
dilute the concentration, as is the case with waste pickle liquor
currently used, the solution can be fed directly from the storage
tanks to the plant.
A bubbler system was incorporated in the design to measure the
level in both ferric chloride tanks.
Positive displacement metering pumps were provided to meter the
iron solution to the various feed points which consisted of the
rapid mix tank, inlet and outlet of primaries and aeration tanks,
and inlet of the final settling tanks. Metering pumps were elec-
tronically paced from the main plant master flow meter. A stand-
by iron solution pump was also included. The solution from the
pumps flows to a rotameter distribution panel where it can be
distributed throughout the plant.
It was designed for polymer to be delivered to the plant in dry
form. An automatic mixer and dispenser were provided to meter the
polymer solution to the various feed points. As in the case of
the iron solution, the feed pumps were paced from an SCR controller
which in turn was paced from the main plant master flow meter. The
rotameter panel for polymer was also provided for distribution
throughout the plant. This panel would split only the diluted poly-
mer.
Numerous programs of varying chemical concentration and feed points
for phosphorous removal were conducted (Figure 5). In March 1974
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ferric chloride was applied to the rapid mix tank, and polymer to
the final sedimentation tank influent. Ferric chloride in the a-
mount of 8.01 nvg/1 as Fe and polymer in the amount of 0.21 mg/1
was applied at a cost of $1,181. Influent phosphorous was 5.5 mg/1
and the final effluent 1.2 mg/1.
In April the polymer was again used in the influent to final sed-
imentation only, with the ferric chloride split, adding 60 percent
to the rapid mix tank and 40 percent to the final sedimentation
influent with no apparent improvement in phosphorus removal. Ferric
chloride in the amount of 8.63 mg/1 as Fe and polymer in the amount
of 0.17 mg/1 was applied at a cost of $1,271. Influent phosphorous
was 5.2 mg/1 and final effluent 1.3 mg/1.
This mode of operation was continued in May and again with no ap-
parent improvement in phosphorus removal.
In June both the polymer and ferric chloride were split with two-
thirds of the chemicals added to the rapid mix and one-third to the
influent to final sedimentation. Although the final effluent phos-
phorous concentration was lower at 0.7 mg/1, it should be noted
that the influent phosphorus was also lower at 3.8 mg/1. The a-
mount of ferric chloride used was 8.38 mg/1 as Fe and polymer ap-
plied was 0.21 for a total chemicals cost of $1,989. The diluted
phosphorous concentration in the influent was due to heavy precip-
itaion and river water backflow. This condition was corrected
shortly thereafter. Perhaps the impact of the tannery coming on
line May 28, 1974 may also have helped in phosphorus removal. How-
ever, the tannery was on limited operation at that time and were
152
-------
buying some of the hides in the blue, which reduced beamhouse lime
waste.
It was apparent that neither split feed, nor chemicals added to the
final sedimentation influent were as effective as adding the total
iron solution to the rapid mix tank prior to primary sedimentation.
Removals were excellent either with or without polymer addition.
It would follow that polymer use was discontinued and the iron
solution added to the rapid mix tank.
After several months of operation with ferric chloride we were con-
tacted by several companies who were contracted to remove waste
pickle liquor from the steel mills in Gary, Indiana. We were able
to purchase the waste pickle liquor for less than the cost of com-
mercial ferric chloride. This has been used for over five years
to date. It has been equally as effective in phosphorus removal
as was ferric chloride.
Also shown on the lower portion of Figure 5 is 1975 data for the
same months as reported in 1974 for comparison. In March 1975
ferrous sulfate in the amount of 4.1 mg/1 as Fe at a cost of $381
was applied to the influent containing 4.6 mg/1 of phosphorus and
resulted in a final effluent phosphorus content of 0.9 mg/1.
In April $352 was spent to apply 4.3 mg/1 of ferrous sulfate as
Fe to an influent containing 5.2 mg/1 of phosphorous which resulted
in a final effluent containing 0.9 mg/1 of phosphorus.
In May $402 spent for 4.8 mg/1 of Fe applied to an influent con-
taining 5.8 mg/1 of phosphorus resulted in a final effluent of 1.1
mg/1 of phosphorus.
153
-------
In June $542 was spent for 6.4 mg/1 of Fe applied to an influent
containing 6.1 mg/1 of phosphorus resulting in an effluent con-
taining 0.9 mg/1 of phosphorus.
It would appear from the data shown in Figure 6 , which shows the
iron used for phosphorus removal, that waste pickle liquor was
actually more effective than ferric chloride in that the amount
applied in milligrams per liter went from 9.3 in 1974-1975 to 6.6
in 1975-1976. We would propose/ however, that the increasing load
from the Eagle Ottawa Leather Co. resulted in much more lime from
their beamhouse operations being discharged to the treatment plant,
which aided in the decrease in the amount of iron required for phos-
phorus removal.
I
To support that theory, Figure 7 shows the amount of flow from
the tannery and the amount of iron applied for phosphorus removal
for the same period of time. As the amount of tannery waste in-
creased, the amount of iron necessary to control phosphorus removal
decreased. The tannery flow went form 190 mg (719,150 cu m) in
1974-1975 to 307 mg (1,161,995 cu m) in 1978-1979. The iron ap-
plied to the total plant flow decreased from 9.3 mg/1 to 1.6 mg/1.
On May 18, 1978 the tannery discontinued the use of the million
gallon equalization tank that had been in use prior to that time
for equalizing the flow to the wastewater treatment plant. Follow-
ing this, the tannery added more lime to their discharge during
periods of dump from the tanhouse portion of their operation. In
the tanhouse operation, a pickling process brings the hides to an
acid condition in preparation for tanning. This waste has a low pH.
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Further documentation in regard to the relationship between volume
of tannery flow and phosphorous removal at the treatment plant for
January and February of 1979 as compared to 1980 is as follows: In
January 1979 the tannery flow was 24.65 mg and 2.21 mg/1 of Fe was
fed resulting in final effluent phosphorus of 0.6 mg/1. To compare,
in January 1980 the tannery flow was only 13.857 and 6.65 mg/1 of
Fe resulted in final effluent phosphorus being 0.6 mg/1. In Feb-
ruary 1979 the tannery flow was 27.424 mg, no Fe feed was required,
and the final effluent phosphorus was 0.5 mg/1. However, in Feb-
reary 1980 the tannery flow was only 18.494 mg and 4.89 mg/1 of
Fe was applied which resulted in final effluent phosphorus concen-
tration of 0.7 mg/1.
SUMMARY
This domestic-industrial activated sludge wastewater plant with
approximately 18 percent of the total flow emanating from a chrome
tanner and 80 percent of the suspended solids and BOD, has achieved
excellent purification. Suspended solids and BOD removals have con-
sistently been above 90 percent. The final effluent phosphorus con-
centration has been under 1.0 mg/1 with removal over 80 percent.
This excellent phosphorus purification has been accomplished with
pickle liquor, all added prior to primary sedimentation, and without
a flocculating aid. Although phosphorus removal was successful with
limited amounts of iron application when the tannery waste was pre-
sent in considerable amount, it was necessary to add much larger a-
mounts of iron solution when the tannery waste was limited or off
entirely. Simple laboratory control has been practiced with analyses
made on the daily composite sewage samples, and iron feed adjusted
based on the prior day's operating results.
157
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THE PHOSTRIP PROCESS FOR PHOSPHORUS REMOVAL
By
Mr. Carl J. Heim
Assistant Staff Engineer
Union Carbide Corporation
Linde Division
Tonawanda, New York
INTRODUCTION
The PhoStrip process is a combined biological-chemical process for the
removal of phosphorus from wastewater. The process works by concentrating
the phosphorus in the wastewater through biological means into a small sub-
stream, to which chemicals are added for precipitation of the concentrated
phosphorus. Normally lime is used for phosphorus precipitation because the
quantity of lime required is proportional to the flow being treated rather than
the phosphorus concentration in that flow. Thus, if the phosphorus in the
wastewater is concentrated into a substream that is 15% of the entering waste-
water flow, the amount of lime required would be only 15% of the lime required
to treat the entire wastewater flow.
In addition to drastically reducing the chemical requirement for phosphorus
removal, the PhoStrip process also produces relatively small quantities of
chemical sludge. Phosphorus is precipitated in a separate reactor in the
process and the resulting chemical sludge does not contain.significant bio-
logical solids. This sludge is inert and stabilization (such as digestion) is
not required prior to disposal. When lime is used for phosphorus precipitation,
a very easily dewatered sludge is produced. The net results are very substantial
savings in both chemical costs and sludge disposal costs.
159
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DESCRIPTION OF THE PHOSTRIP PROCESS
A flow schematic of the PhoStrip process is shown in Figure 1. In the
process, return sludge is mixed with plant influent and aerated exactly as in
a conventional activated sludge system. While under aeration, the micro-
organisms have the capability of removing essentially all of the soluble phos-
phorus from the wastewater because of special conditioning received in the
PhoStrip process. The phosphorus removed in the aeration basin is incorporated
into the sludge in the form of stored polyphosphates. The phosphorus content
of the sludge leaving the aeration basin can be more than twice that of sludge
from a conventional system. Removals of biological oxygen demand and sus-
pended solids in the aeration system are unaffected by PhoStrip.
The phosphorus-laden sludge is separated from the phosphorus-free effluent in
the secondary clarifier. The sludge withdrawn with the clarifier underflow is then
either sent directly back to the aeration basin, wasted from the system (excess
biological sludge quantities are not affected by the PhoStrip process) or sent to
a stripper tank, where it is held under anoxic conditions for several hours.
While under anoxic conditions, the microorganisms release their stored phospho-
rus in soluble form. The released phosphorus is "washed" from the sludge blanket
by an elutriation stream and withdrawn as a supernatant from the stripper tank.
This supernatant stream is then fed to a reactor-clarifier where the phosphorus
is precipitated with lime. Typically, the supernatant flow is 10-20% of the influent
flow. Therefore, as explained previously, lime requirements are reduced by
160
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Influent
Aeration
Basin
Direct Recycle
Reactor-
Clarifier
Supernatant
Effluent
\
Waste
Sludge
Stripper Feed
Anoxic
Stripper
Tank
Elutriation Stream
Waste Chemical Sludge
Stripper Underflow
Figure 1. Phostrip System Flow Schematic
161
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80-90% and chemical sludge quantities are also reduced. The inert chemical
sludge is withdrawn from the bottom of the reactor-clarifier. The overflow
from the reactor-clarifier, which has a relatively low phosphorus concentration,
is used as the elutriation stream.
Sludge is withdrawn from the bottom of the anoxic stripper tank at the same
rate as it is fed to the tank to avoid solids buildup. This sludge is returned
to the aeration basin where phosphorus uptake is resumed.
The PhoStrip process typically produces an effluent with a total phosphorus
concentration of 0.5-1.0 mg/1. The effluent soluble phosphorus concentration
normally ranges from 0.1-0.5 mg/1. The PhoStrip process operates over the
normal range of activated sludge system operating conditions and can be used
with either air or oxygen activated sludge systems.
THEORY
Biochemical Aspects
The biochemical phenomemon responsible for the PhoStrip process has not
been fully defined. Results of experimental work have led .to the formulation
of the following mechanisms for the observed phenomenon.
Organisms containing high intracellular phosphate concentrations have
been isolated from wastewater treatment systems exhibiting high phosphorus
removal rates. Typical of these isolates are organisms of the genus Acineto-
bacter. The organisms of this genus have demonstrated the ability to take
162
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up and release phosphorus as a function of the aerobic-a noxic cycle, while
in pure culture form. The interior of the cells have been characterized as
containing very large volutin (polyphosphate) granules while under aerobic
conditions. The size of these granules diminished as the culture was main-
tained in an anoxic environment. This indicates a transfer of phosphorus
from the volutin granules into solution. These particular organisms are so
abundant in activated sludge systems that the Water Research Centre Labora-
tory at Stevenage, England, has utilized pure cultures to simulate activated
sludge systems. These organisms are also obligate aerboes preferring Krebs
cycle intermediates and acetates as substrates for metabolism.
It is believed that the anoxic period of the PhoStrip process forces these
strict aerobes to undertake a sequential series of reactions which result in
their forming polyphosphate granules while in the aerobic period. This results
in a set of aerobic organisms that can compete more effectively with facultative
organisms in a cyclic aerobic-anoxic environment. The polyphosphate granules
within the cell may provide phosphorus and energy to convert ADP to ATP during
(2 3)
the anoxic period through the catalysis of the polyphosphokinase enzyme . '
Substitution of polyphosphate for ATP in biochemical reactions during anaero-
(4)
biosis is also possible. (A third potential pathway of phosphorus release
utilizing the phosphatase enzyme has not yet been delineated.)
In the first mechanism, conversion of ATP to ADP during the anoxic period
results in the release of phosphorus from the cell as well as providing a source
of energy. This energy is utilized by the obligate aerobes to continue some of
their metabolic functions. The fact that the addition of acetates increases the
163
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rate of phosphorus release suggests an interaction between these organisms
and the facultative microbes present in activated sludge. Under anoxic condi-
tions, the facultative aerobes produce acetates which enhance the rate of phos-
phorus release by the oligate aerobes. When the sludge leaves the anoxic
environment and enters aerobic conditions, the ATP content within the cell
is low because the reaction of ATP—>• ADP + P is a high rate reaction relative
to the formation of ATP from polyphosphates.
In the second, direct substitution mechanism, the energy of the poly-
phosphate-phosphorus bond is utilized in place of the ATP bond energy. The
phosphorus would be directly released to solution from the polyphosphate
molecule. If direct substitution is the major means of phosphorus release,
the above ATP to ADP reaction would also occur producing a low ATP/ADP
ratio in the cell.
Under aerobic conditions, the strict aerobes- oxidize stored metabolites
and other substrates to provide energy to increase the ATP content of the cell.
After a very short time, the ATP/ADP ratio in the cell becomes high enough
to trigger the formation of polyphosphate via the reversible polyphosphokinase
enzyme. This results in the formation of polyphosphate granules which are
stable storage products in an aerobic environment.
The performance of the PhoStrip process is consistent with the theory.
The theory implies a temperature dependency. In fact, an Arrhenius type
relationship has been established. This theory also indicates that the rate
of phosphorus release per unit mass of organisms is a function of the duration
164
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of the anoxic period, as well as the quantity and activity of facultative
organisms. The activity of the facultative bacteria can be related to the
Food-to-Microorganism ratio (F/M) of the activated sludge system, while
quantity is related to the concentration of sludge in the stripper tank. Since
strict aerobes are implicated in the above theory, too long an anoxic period
relative to the aerobic period could cause the organisms to cease phosphorus
uptake. Experimentally determined operating limits for such a response do
exist. However, there is a broad spectrum of conditions under which good
performance has been established.
The finite capacity of these organisms for phosphorus storage results
in a loading requirement which must not be exceeded if a high degree of
phosphorus removal is to be achieved. Different activated sludge systems
have exhibited different maximum levels of phosphorus per unit mass of
MLVSS. This maximum P/VSS ratio has been observed to be a function
of the viable organism content of the volatile suspended solids. The P/
VSS ratio observed in efficiently operating PhoStrip Systems depends on the
phosphorus available in the feed, the maximum P/VSS ratio attainable,
and the environmental conditions presented earlier.
Ideally, all the phosphorus in the feed would be incorporated into the
cell mass and wasted from the system as biological sludge. This mode of
operation would eliminate the need for chemical precipitation facilities and
significantly reduce the operating cost of the process. However, there are
factors which prevent this from being realized in all but a few instances.
165
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First, effluent quality is a function of the soluble and particulate phosphorus
content. Even if an effluent soluble PQ^ level of ^^.01 mg/1 were achieved,
a 20 mg/1 VSS in the effluent would limit the phosphorus to VSS ratio to <0.05
in order to achieve an effluent <^ 1.0 mg PO.-P/l. Second, for a given P/
VSS level;, a specific quantity of sludge must be wasted as dictated by phos-
phorus mass balances in order to remove enough phosphorus to achieve the
desired effluent. The amount wasted generally depends on the F/M (SRT) of
the system. In most cases a high degree of phosphorus removal could only be
achieved at very high F/M (low SRT) values because of the low P /VSS levels
necessary to satisfy effluent criteria as presented above. Third, bio-chemical
sludges tend to release phosphorus when digested. If high P /VSS levels
are employed for phosphorus removal, large quantities of phosphorus could
return to the head end of the plant. This level of phosphorus return would
require a significant increase in sludge wasting unless some method of chemi-
cal precipitation were employed.
The PhoStrip System is normally designed for a phosphorus content of
0.03-0.04 Ib. P/lb. VSS in the sludge in order to achieve effluents of less
than 1.0 mg PO -P/l. • The phosphorus that is not removed through wasting is
precipitated from the supernatant stream leaving the stripper tank. The
relative amounts of phosphorus removed through sludge wasting and precipi-
tation depend on the F/M (SRT) of the activated sludge system and the BOD5 /P
level in the wastewater. The ratio of phosphorus removal by precipitation to
166
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the overall phosphorus removal can range from 0 to 0.9+. Each wastewater
will result in different values of this ratio depending on the design conditions
of the activated sludge system and the method of waste sludge disposal.
Chemical Precipitation of Phosphorus
Lime was chosen as the precipitant because of its pH functionality.
Unlike alum and ferric chloride, the gross quantity of lime required for pre-
cipitation of phosphorus in water is dependent only on the amount and alkalinity
of the water not the concentration of phosphorus. Further reduction in chemical
requirements can be achieved by precipitating phosphorus at lower pH levels
(8.5 - 9.0). At these pH levels, the stripper supernatant after lime addition
may typically contain 2-5 mg soluble PO^-P/l. A lowerphwillalsoresultin sub-
stantially less chemical sludge to be handled because less calcium carbonate
and no magnesium hydroxide are formed. The chemical sludge production will
be typically less than 50 percent of that produced at a pH = 10.5. This material
could be used as an agricultural fertilizer because of its high phosphate content.
FULL SCALE PERFORMANCE
The PhoStrip system has been demonstrated at two localities under full
scale conditions and 9 pilot plant locations. These two full scale plants
were Seneca Falls, NY and Reno/Sparks, Reno, Nevada.
167
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SENECA FALLS. NY
The wastewater treatment facility at Seneca Fall, NY is an activated
sludge treatment plant with two trains and a total capacity of 3 .5 MGD
3
(13,247 m /day). The plant consists of a bar screen, comminutor, two cir-
cularprimary clarifiers, twocompletely mixed aeration basins with mechanical
aerators, two rectangular secondary clarifiers and a chlorine contact chamber. The
The wastewater is largely domestic in character with a BOD of approximately
160 mg/1; total dissolved solids of 680 mg/1 and total phosphorus of 6.3 mg/1.
Conversion of the plant to the PhoStrip process was facilitated by the
3
fact that, at the time of the study, the raw wastewater flow was only 3800 m /G
(1 mgd). This enabled the plant to handle the full plant flow through one of
the two reactor trains, thus freeing a primary clarifier to provide the anoxic
environment required for the return sludge to release excess phosphorus.
The tank providing this anoxic zone has been labelled the "stripper tank".
The use of a single train to treat the entire wastewater flow also permitted
the test to be run on a system that was much nearer the design hydraulic loading
for the Seneca Falls plant. The use of the primary clarifier as the stripper tank
was expeditious; however, it was significantly oversized relative to the waste-
flow entering the aeration basins. Table 1 presents a concise summary
of the data obtained during the first thirty days of operation at Seneca Falls.
It is evident from this table that substantial savings have been demonstrated.
The amount of lime has been greatly reduced since the supernatant from the
168
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Table 1. Results of Phosphorus Removal Test
at Seneca Falls, N.Y.
Plant Flow, m3/d (mgd)
Return Flows, percent of raw flow:
Sludge to Stripper
Sludge to Aeration from Stripper
Supernatant to Primary Clarifier
Total Suspended Solids, mg/1:
Mixed Liquor
Sludge to Stripper
Sludge to Aeration from Stripper
Influent, mg/1:
Total Phosphorus
Effluent, mg/1:
BOD5
Total Phosphorus
Plant Performance:
BOD5 Removal, percent
Total Phosphorus Removal, percent
Lime Dose, Stripper Supernatant, mg/1 of supernatant
(as CaO)
Lime Dose, prorated to mg/1 of raw flow (as CaO)
3400 (0.9)
24
10
14
1,440
7,840
15,910
158
6.3
.6
98
91
170
24
169
-------
PhoStrip stripper is only fourteen percent of the incoming flow. Calculated on
the basis of the incoming flow, the lime dose would be 24 mg/1 as CaO.
When compared to conventional lime requirements of 300-660 mg/1 for post
precipitation to obtain the same total phosphorus effluent concentration of
less than 1 ppm (0.6 ppm), the savings are quite apparent. This represents
the period of operation during which the performance of the process was inten-
sively monitored. ,The recycle flow rates presented are typical of a system
utilizing sludge thickening in the stripper tank to produce the phosphate-
enriched supernatant. The data on plant performance indicates that very high
removals of both BODS and phosphorus were achieved. The lime dosage is
reflective of the chemical requirements anticipated for many full scale systems.
RENO/SPARKS. RENO. NEVADA
The Reno/Sparks facility is designed to process an average flow of
3
76,000 m /d (20 mgd) and discharges into the Truckee River. The system con-
sists of an aerated grit chamber, three primary clarifiers, three activated sludge
trains and three secondary clarifiers. The PhoStrip System initially operated
by Kennedy Engineers, San Francisco, California, on one third of the total av-
3
erage plant flow (25,000 m /d) by using the sludge recycle option of operation
(Figure 2). In this option, the stripper is operated in a thickening mode and a
portion of the stripper underflow is recycled back to the stripper feed. The rea-
son for recycling the underflow is to increase the supernatant phosphorus by mix-
ing high P/low P streams. (This mode of operation produced an elutriation effi-
ciency of approximately 38%, where elutriation efficiency, E, is defined as the
170
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Wastewater
Primary
Clarifier
Lime
Reactor
Clarified
\| Waste
Sludge
Chemical
Aeration
(Secondary
Clarifier
Effluent
Direct Recycle
Stripper
Supernatant
Stripper
Stripper
Feed
Waste
Sludge
Sludge
Recycle
Stripper Return
Figure 2. Sludge Recycle Option
171
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amount of phosphorus removed by the stripper overflow per day divided by the
amount of phosphorus released in the stripper per day. )
On June 25, 1975, Union Carbide Corporation began its evaluation of the
PhoStrip process on the full scale plant at Reno/Sparks, Nevada. A set of
conditions was established on the full scale (Table 2) -and the system was
allowed to come to steady state. After steady operating conditions were
achieved, a period of intensive evaluation followed. Table 3 presents the
results of analyses performed at Reno/Sparks during this phase. Figures 3 &
4 present the influent and effluent phosphorus levels during the testing period
and their variation with the flow to the plant. The system demonstrated excel-
lent effluent quality in all respects, and as evident in the figures, total phos-
phorus levels were consistently 1 mg/1 or less.
In an effort to improve the elutriation efficiency a low phosphorus elutria-
tion (LPE) modification was employed. The cross sectional area requirement
for the stripper as dictated by the limiting-flux theory is reduced relative to the
sludge recycle system. Since the primary clarifier (stripper tank) at the Reno/
Sparks plant had a fixed cross-sectional area,the solids flux considerations
3
indicated that two-thirds of the plant flow (50,000 m /d) could be treated
with the available area. As a result, the system was modified according to
Figure 1, which was referred to earlier. Table 4 presents the operating condi-
tions for this two week test period (Jan. 18-30, 1977) and Figure 5 graphically
displays the influent and effluent phosphorus concentration. Again, the efflu-
ent total phosphorus levels were usually 1.0 mg/1 of phosphorus or under.
172
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Table 2. Operating Conditions for the Phostrip
Sludge Recycle System - Full Scale Testing
at Reno/Sparks, Nevada (9/13/75-9/27/75)
Parameter
Flow Rates (m3/day)
Feed, (Q)
Recycle to Stripper (R,)
Stripper Underflow (R^)
Stripper Supernatant *
Recirculation Rate (R2)
Waste Sludge Rate
Aeration Time, Hr. (based on Q)
Anoxic Period, Hr. (based on R3)
MLSS, mg/1
MLVSS, mg/1
RjSS, mg/1
RiVSS, mg/1
R3SS, mg/1
R3VSS, mg/1
-TSS Stripper Supernatant, mg/1
VSS Stripper Supernatant, mg/1
D.O., End of Aeration, mg/1
D.O. , Rj, mg/1
\ D.O., R3, mg/1
pH, End of Aeration Basin
PH, Ri
pH, RJJ/
pH, Stripper Supernatant
Temperature, "C
F/Ma (kg COD/day/kg MLVSS)
Clarifier Overflow Rate, m/day
Clarifier Blanket Level, m.%
Minimum
14, 690
5,180
2,330
2,850
4,230
639
10.2
16.
_
-
3,060
2,480
9,620
7,700
65
50
_
0.4
0.3
_
6.8
6.4
6.6
23
-
22.4
0.08
Time
Weighted
Maximum Mean
25,060
7,340
4,150
3,200
2,420
639
6.0
9.4
_
-
4,620
3,740
9,120
7,300
90
69
1.5 (0.7-2.2)
0.7
0.3
7.0
6.8
6.4
6.5
23
—
38.2
0.09
22,460
6,830
3,630
3,110
2,850
639
7.1
11.0
1,150
900
4,230
3,420
9,250
7,340
84
64
_
0.6
0.3
—
-
-
—
23
0.96
34.3
0.09
173
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Table 3. Analytical Results for the Phostrip
Sludge Recycle System Full Scale Testing
at Reno/Sparks, Nevada (9/13/75-9/27/75)
Parameter
Minimum Maximum
Flow
Weighted
Mean
COD, mg/1
Influent
Effluent
mg/1
Total Suspended Solids,
Influent
Effluent
Effluent Volatile Suspended Solids,mg/1
Total Phosphorus, mg P/l
Influent
Effluent (ortho)
Stripper Supernatant
Stripper Underflow
Filtered Stripper Underflow
Filtered Aeration Effluent (ortho)
Secondary Clarifier Underflow
P/VSS
Secondary Clarifier Underflow
Stripper Underflow
187
40
19
13
9.6
1.0 (.
44
257
67
104
0.042
0.025
3)
266
37
13
10
9.1
0.8
41
240
55
- (-
161
(.4)
04)
0.043
0.025
253
37
113
13
10
9.2
0.8 (.4)
42
247
58
113
0.043
0.025
174
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=3
cr
o
X
Q.
05
O
X
Q.
22-
20 -
8 J
2 -
0 -
8 -
6 -
4 -J
0
INFLUENT TOTAL = A
EFFLUENT TOTAL = D
EFFLUENT ORTHO= O
7 18 19 20 21 22 23 24 25 26 27
SEPTEMBER, 1975
Figure 3. Reno/Sparks Full Scale Phosphorus Data Obtained
during Minimum Flow Period (16% of the Total
Volume Treated by the Phostrip System)
175
-------
en
OL
O
m
Q.
CO
O
IE
Q_
22-
20-
8 -
6 -I
4 -
2 -
0 -
8 -
6 ~
4 -I
2 H
INFLUENT TOTAL =
EFFLUEN'T TOTAL «D
EFFLUENT ORTHO =O
2 13 14 15 16 17 IS 19 20 2! 22 23 24 25 26 27
SEPTEMBER, 1975
Figure 4. Reno/Sparks Full Scale Phosphorus Data Obtained
during Maximum Flow Period (84% of the Total
Volume Treated by the Phostrip System)
176
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12-,
I-
10-
9-
8-
7-
cc
o
X
O
I
a.
6-
5-
4-
3-
2-
1-
INFLUENT=A
EFFLUENTS =B
EFFLUENT*2 =O
X>
O- - _ _
O
I I \ II 1 I I I Till
18 |9 20 21 22 23 24 25 26 27 28 29 30
JANUARY, 1977
Figure 5. Reno/Sparks Full Scale Phosphorus Data for LPE System
177
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A comparison between the LPE and sludge recycle system indicates that the
LPE System was capable of producing the same quality effluent while utilizing
the same stripper, but handling twice the flow.
The main reason for this is an improvement in elutriation efficiency with
the LPE System ( £ = 0.59 vs. £ = 0.38). This improvement translates to a
decrease in the initial capital cost due to the decrease in tankage.
178
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ECONOMIC EVALUATION
COMPARISON OF OPERATING COSTS FOR PHOSPHORUS REMOVAL SYSTEMS
Table 4 shows a comparison of operating costs for various phosphorus
removal systems. Included in the comparison are conventional chemical pre-
cipitation with lime, alum, ferric chloride and pickle liquor, as well as the
PhoStrip process with lime or pickle liquor addition. The costs are based on
an alkalinity of 250 mg/1, and an influent phosphorus concentration of 1 mg/i.
Chemical requirements and costs for the conventional phosphorus removal
systems were taken from the EPA Process Design Manual for Phosphorus
Removal (1976) and have been adjusted to 1st quarter 1980. Chemical sludge
disposal costs were assumed to be $100/ton of dry solids.
It is apparent from inspection of Table 5 that the use of the PhoStrip process
drastically reduces the operating costs for phosphorus removal. For the example
case shown, operating costs are reduced by approximately 40-55% compared
to a conventional system using pickle liquor, which has the lowest operating
cost of the conventional systems.
CASE STUDY
The following economic study has been taken verbatim from the EPA Bio-
logical-Chemical Process for Removing Phosphorus at Reno/Sparks, NV
publication, and is for illustrative purposes only.
179
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Table 4. Operating Conditions for Full Scale
Testing at Reno/Sparks, Nevada
Phostrip LPE System (January 18-30, 1977)
PARAMETER
MINIMUM
TRAIN I/TRAIN 2
MAXIMUM*
TRAIN I/TRAIN 2
FLOW
WEIGHTED MEAN
TRAIN I/TRAIN 2
Flow Rates, m /day
Feed 0. (each train) 17280/17280 29380/29380 22460/22460
Recycle to Stripper. RI 1987/2160 3200/3370 2510/2680
Stripper Underflow, R3 1210/1470 2250/2250 1640/1810
Stripper Supernatant, S 6570 7000 6740
Elutrlatlon, EL 5270 5620 5440
Total Aerobic Recycle, Rj + Rdirect - ~ 4490/5530
Sludge Wasting - - 331/418
Aeration Time, Hrs. (based on Q) 9.0/9.0 5.1/5.1 6.8/6.8
Anoxic Period, Hrs. (based on R$) 11.6 7.0 9.5
MLSS, mg/1 1230/1280 1110/1140 1170/1220
VSS/TSS 0.8 0.8 0.8
RlSS, mg/1 5750/5460 6770/6720 6210/6030
VSS/TSS 0.78 0.78 0.78
R3SS, mg/1 8930 8310 8650
R3VSS, mg/1 7360 6590 7010
TSS Stripper Supernatant, mg/1 59
VSS Stripper Supernatant, mg/1 54
pH, Mixed Liquor, mg/1 7.1/7.0 7.0/7.0
Temperature (Influent), *C 13 13 13
F/Ma (kg BODs/dayAg MLVSS) 0.45 0.88 0.62
44.8/44.8 34.3/34.3
<0.2
Secondary Clarifier Overflow Rate,m/day 26.4/26.4
Clarifier Blanket Level, m.
duration at max. flow y 11 hrs/day
180
-------
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ADRIAN. MICHIGAN
The proposed Adrian WWTP design is for a two-stage activated sludge
system. The first stage will be used for carbonaceous removal and the second
stage will convert ammonia to nitrate. The PhoStrip process will be operated
in conjunction with the first stage aeration system. The main advantage of
the PhoStrip System is dosing only 10-15% of the sewage flow with chemicals
as compared to the conventional method of chemical treatment which uses
addition of chemical to the entire flow of sewage. Most of the operating ex-
penses of phosphorus removal is the chemical cost and the PhoStrip System
significantly reduces this cost. (Tables 6 & 7)
An economic evaluation was made comparing PhoStrip against the traditional
chemical addition methods using ferric chloride and alum. The cost-effective
analysis included initial installment cost and total annual costs which includes
capital cost amortized over 20 years at 6.125%interest; chemical cost; operating
labor; maintenance and repair costs; and sludge disposal costs.
The PhoStrip costs were based on (chemical) treatment of 15% of the maximum plant
flow of 7 mgd , or 1.0 mgd. The cost of the two traditional chemical processes
were based on total plant flow of 7 mgd. The bench scale lime dosage test
conducted during the pilot plant operation established a lime dosage of 250 mg/1
to produce the desired treatment. The dosage required for treatment with the
traditional chemicals were: 90 mg/1 of ferric chloride and 135 mg/1 of alum.
182
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Table 6. Cost Comparison between Phostrip and
Chemical Addition for Phosphorus Removal
at Adrian, Michigan
Design Flow = 7 mgd
Influent P = 10 mgd
Effluent P = 1 mg/1
Item PhoStrip Ferric Chloride Alum
A. Installed Investment1 $520,000 $ 60,000 $ 65,000
B. Annual Costs
1. Amortized Investment2 (A x 0.08897) 46,265 5,338 5,783
2. Chemical Costs
a. Lime3 20,000
b. Ferric Chloride4 — 105,500
c. Alum5 — — 115,000
3. Operating Labor, Maintenance
& Repair 8,006 3,000 3,500
4. Sludge Disposal Cost O&M at 800T/yr at835 T/yr at 525 T/yr
a. Anaerobic Digestion at $5/ton 4,000 4,175 2,625
b. Transport of Liquid Sludge by
Tank Truck at $15/Ton 12,000 12,525 7,875
TOTAL ANNUAL COST 90,265 130,538 134,783
$/mg $33.50 $51.. 10 $52.75
See Table 7 for cost breakdown.
2
Assumes a 20-year equipment life and 6-1/8% capital cost.
o
Based on a 250 mg/1 lime dosage, 15% Qt supernate flow, and a lime
cost of $50/ton delivered, (where Qt is the total influent flow to the plant.)
4
Based on a 90 mg/1 FeClg dosage, 7 mgd flow, and a FeCis cost of
$110/ton delivered.
Based on a 135 mg/1 alum dosage, 7 mgd flow, and an alum cost of
$80/ton delivered..*
183
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Table 7. PhoStrip Cost Comparison
Equipment Cost '(PhoStrip) Cost
1. Stripper Tank
a. Concrete 65-ft. dia. at 20-ft. SWD $150,000
b. Mechanism & Warranty (supplied by Union Carbide) 245,000
2 . Lime-Mix Tank
a. Concrete 9-sq. ft. at 12-ft. SWD 57,500
b. Mixer 2,500
3. Pumps
a. Stripper supernatant Pumps 2,000
b. Anaerobic RAS Pumps 2,000
c. Stripper Waste Pumps 1,000
4. Lime Feed Equipment* (50 ton Bin, Feeder, Slaker) 60,000
Total Installed Cost $520,000
* Cost taken from EPA Manual "Phosphorus Removal", p. 10-32
ENR = = 1.53
1643(1971)
Equipment Cost (Ferric Chloride)
1. Bulk Storage 2/8000 gal. tanks $ 25,000
2. Pumps
Transfer 15,000
Feed
3. Dilution and Feed Tanks, Agitation, Piping 20,000
Total Installed Cost $ 60,000
Equipment Cost (Alum)
1. Bulk Storage 4/8000 gal. tanks $ 50,000
2. Pumps
Transfer 15,000
Feed
Metering
Total Installed Cost $ 65,000
184
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The estimated total annual cost of increasing the capacity of the existing
plant and adding the capability for phosphorus removal are: $85,565 per year
using the PhoStrip process; $129,163 per year using the ferric chloride process;
and $136,183 per year using the alum process.
185
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REFERENCES
1) Fuhs, G. W., and Min Chen, "Microbiological Basis of Phosphate in
Activated Sludge Process for Treatment of Wastewater, " Microbial
Ecology, 1976.
2) Kornberg, S. R., "Adhenosine Triphosphate Synthesis from Polyphosphate
by an Enzyme from Eschericia Coli", Biochimica et Biophysica, Acta, 26.,
294, 1957.
3) Buller, L., "A Suggested Approach to ATP Regeneration for Enzyme Tech-
nology Applications", Biotechnology and Bioengineering, 19, 591, 1977.
4) Fox, J. L., "Pyrophosphate Drives Biochemical Reaction", Chemical &
Engineering News, 22, April 25, 1977.
-L O U a US GOVERNMENT PRINTING OFFICE 1980-657-165/0077
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