| - AS 02-5
- THIS FILING IS SUBMITTED ON RECYCLED PAPER
- BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
- A. Ammonia Effluent Limitations
- C. Mixing Zone and ZID
- A. Facility and Process Description
- C. Description ofArea Affected
- D. Description ofDischarge
- A. In-Process Reductions
- B. Pretreatment
- C. Post-treatment
- Alternative #1
- Alternative #2
- Alternative #3
- Exhibit List
- Group, Inc., Henry Facility
- MIXING ZONE/ZID ISSUES
- ILLINOIS RIVER AT HENRY, ILLINOIS
- NOVEON, INC.
- GENERAL CONDITIONS
- River Characteristics
- OCTOBER 25, 1989 DISPERSION STUDY
- Effluent
- River
- Plume
- 3,000
- CONDUCTIVITY
- EFFLUENT
- DISPERSION
- RATIO
- 900 liii 89.8
- 1,000 2.0 49.9
- ZID DISTANCE (It)
- Plant Effluent
- DMR Support Data - 2001
- Plant Effluent
- DMR Support Data - 2001
- DMR Support Data - 2001
- Plant Effluent
- Plant Effluent
- Plant Effluent
- DMR Support Data - 2001
- Plant Effluent
- Plant Effluent
- Plant Effluent
- Plant Effluent
- Prepared for:
- BF GOODRICHHenry, Illinois
- Prepared by:
- February 1997
- 9387.01
- TABLE OF CONTENTS (Continued)
- Pate No.
- - Follows
- Follows
- 1.2 SCOPE OF WORK
- FIGURE 1-2
- BLOCK FLOW DIAGRAM OF ALKALINEAIR STRIPPING TREATMENT ALTERNATIVES
- (Nos• 1, 2, and 3)
- FIGURE 1-3
- BLOCK FLOW DIAGRAM OF STRUVITEPRECIPITATION TREATMENT ALTERNATIVE
- (No.4)
- BLOCK FLOW DIAGRAM OF BIOLOGICALNITRIFICATION TREATMENTALTERNATIVE
- (No.5)
- FIGURE 1-5
- BLOCK FLOW DIAGRAM OF BIOLOGICALNITRIFICATION TREATMENT ALTERNATIVE
- (No.6)
- 2.1.3 Single-Stage Biological Nitrification of Non-PC Wastestreams
- Combined with Separate Biological Treatment of the PC Wastestream
- 2.1.3.4
- 2.1.6 Ion Exchange Treatment of Final Effluent
- 3.0 BATCH TREATABILITY TEST RESULTS
- pH, s.u.
- pH, s.u.
- • 93H2S04
- pH, su.
- 3.2 STRUVITE PRECIPITATION
- pH, s.u.
- Figure 3-4 pH Adjustment of Combined Wastestream
- BREAKPOINT CHLORINATION OF SECONDARY CLARIFIER EFFLUENT
- 3.4 ION EXCHANGE TREATMENT OF FINAL EFFLUENT
- 4.1 BIOLOGICAL NITRIFICATION OF COMBINED WASTESTREAM
- MEMORANDUM
- BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
- ) ASO2-____
- ) (Adjusted Standard)
|
RECEIVED
CLERK’S OFFICE
BEFORE THE ILLINOIS POLLUTION CONTROL BOAR~y
22 2002
IN THE MATTER OF:
Petition ofNoveon, Inc.
for an Adjusted Standard from
35
Ill. Adm. Code 304.122
)
)
AS 02-5
)
)
)
STATE OF IWNOIS
Pollution Control Board
NOTICE OF FILING
TO:
Dorothy M. Gunn, Clerk
Illinois Pollution Control Board
James R. Thompson Center
100 West Randolph Street
Suite 11-500
Chicago, IL 60601
Bradley P. Halloran
Hearing Officer
Illinois Pollution Control Board
James R. Thompson Center
100 West Randolph Street
Suite 11-500
Chicago, IL 60601
Connie L. Tonsor
Special Assistant Attorney General
Illinois Environmental Protection Agency
1021 N. Grand Avenue East
Springfield, IL 62794-9276
PLEASE TAKE NOTICE
that on Wednesday, May 22, 2002, we filed the attached
Petitjon for Adjusted Standard
with the Illinois Pollution Control Board, a copy of which is
herewith served upon you.
Richard J. Kissel
Mark Latham
GARDNER, CARTON & DOUGLAS
321 North Clark Street
—
Suite 3400
Chicago, IL 60610
(312) 644-3000
Respectfully submitted,
NOVEON, INC.
By:
~
One ofIts Attorneys
THIS FILING IS SUBMITTED ON RECYCLED PAPER
RECEIVED
CLERK’S OFFICE
BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
f~j3~’(
2 2 2002
IN THE MATTER OF:
)
STATE OF IWNOIS
)
Pollution Control Board
Petition ofNoveon, Inc.
)
)
ASO2-____
)
(Adjusted Standard)
for an Adjusted Standard from
)
35 Ill. Adm. Code 304.122
)
PETITION FOR
ADJUSTED STANDARD
Noveon, Inc., flk/a The BFGoodrich Company (“Noveon”), through its undersigned
attorneys, respectfully petitions the Illinois Pollution Control Board (“Board”) for an adjusted
standard pursuant to 35 Iii. Adm. Code 104 and Section 28.1 ofthe Illinois Environmental
Protection Act (“Act”). Specifically, Noveon requests an adjusted standard from 35 Ill. Adm.
Code 304.122(b) for the effluent from Noveon’s Henry, Illinois Plant.
PROCEDURAL
BACKGROUND
On August 30, 1989, Noveon submitted a renewal application for NPDES Permit No.
IL0001392, governing the wastewater discharge from the Noveon plant located in Henry, Illinois
(the “Henry Plant”). By letter dated December 28, 1990, the Illinois Environmental Protection
Agency (“Agency”) re-issued a final NPDES permit for the Henry Plant. In response to the re-
issued NPDES permit, on January 24, 1991, Noveon initiated a timely permit appeal (PCB 91-
17).
Noveon filed the appeal based on, among other grounds, the inclusion ofammonia
nitrogen effluent limitations that had not been included before in any ofthe previously issued
Henry Plant NPDES permits. The Agency claimed that the inclusion of an ammonia nitrogen
effluent limitation was based on the regulatory requirements of 35 Ill. Adm. Code 304.122(b).
That provision of the Board’s regulations states that:
Sources discharging to the Illinois River, the Des Plaines
River downstream ofits confluence with the Chicago River
System or Calumet River System and whose untreated
waste load cannot be computed on a population equivalent
basis comparable to that used for municipal waste treatment
plants and whose ammonia nitrogen discharge exceeds 45.4
kg/day (100 poundsper day) shall not discharge an effluent
ofmore than 3.0 mg/L oftotal ammonia nitrogen as N.
Id.
It was Noveon’s position in the permit appeal that this provision was not applicable to the Henry
Plant and that the Agency was without basis to include such a limitation in the NPDES Permit.
Noveon contended that, since the Henry Plant’s untreated waste load could be readily calculated
under 35 Ill. Adm. Code 304.122(a) on a population equivalent (“PE”) basis, 35 Ill. Adm. Code
304.122(b) was inapplicable because anotherprovision ofthe Board’s regulations, 35 Ill. Adm.
Code 304.122(a), should be considered with regard to the Henry Plant’s discharge. 35 Ill. Adm.
Code 304.122(a) provides that:
No effluent from any source which discharges to the Illinois River,
the Des Plaines River downstream ofits confluence with the
Chicago River System or Calumet River System, and whose
untreated waste load is 50,000 or more population equivalents shall
contain more than
2.5
mg/L of total ammonia nitrogen as N during
the months ofApril through October, or 4 mg/L at other times.
The untreated waste load for the Henry Plant is less than 32,000 PE. Thus, pursuant to Section
304.122(a), no effluent limitation for ammonia should apply to the Henry Plant because its
untreated waste load can be calculated on a PE basis, and the PE is less than 50,000.
During the mid-1970’s the Agency did raise the applicability of35 Ill. Adm. Code
304.122(b) in a draft NPDES Permit for the Henry Plant, only to remove the proposed ammonia
effluent limit and issue a permit without this condition. Nothing has changed with respect to the
2
discharge from the Henry Plant that would warrant a change in that Agency decision regarding
the applicability ofthis section.
Following initiation of the permit appeal proceeding and aftertwo days ofhearing were
conducted, Noveon and the Agency entered into negotiations to resolve the issues raised in the
permit appeal. After lengthy discussions with the Agency, the parties agreed that the appropriate
course of action would be forNoveon to file a variance petition with the Board to enable Noveon
to review and evaluate treatment alternatives that might allow the Henry Plant to reduce the
levels ofammonia in its wastewater discharge. Consequently, the permit appeal proceeding was
stayed by agreement ofthe parties through a series ofdecision deadline waivers, with periodic
status reports to the Board, and a variance petition (PCB 92-167) was filed on October 30, 1992.
By order dated November 19, 1992, the Board issued an order accepting the variance petition for
hearing.
As discussed in detail later in this petition, as part of the “study variance” proceeding,
Noveon and its consultants continued to review and evaluate different aspects of ammonia
reduction and treatment technologies that would, perhaps, reduce the ammonia nitrogen in the
wastewater from the Henry Plant. In addition, Noveon continued its internal studies focused on
determining whether it could take any actions to eliminate, recover or recycle the precursors to
ammonia contained in the Henry Plant wastewater. Because ofthe complexity of the various
studies, they took longer to complete than was anticipated. A series ofstatus reports were also
filed with the Board as part of the variance proceeding, detailing the progress Noveon made in
evaluating the ammonia issue at the Henry Plant. Noveon kept the Agency apprised ofits
efforts, and a series ofprogress meetings took place between representatives ofNoveon and the
Agency during the course ofthe various studies.
3
At the numerous meetings between the parties, the various reports detailing the potential
source reduction options, pretreatment options and treatment alternatives were discussed. Based
oii those studies and the evaluation ofthe various options reviewed, Noveon and its consultants
have concluded, and the evidence presented in this proceeding will show, that none ofthe
available treatment technologies are both economically reasonable and technically feasible for
Noveon to significantly reduce the ammonia in the wastewater from the Henry Plant to levels
that would achieve compliance with 35 Ill. Adm. Code 304.122(b). Consequently, a variance
would not be the appropriate vehicle for Noveon to obtain relief since that would require
eventual compliance with the standard from which relief was requested. Accordingly, the
Agency and Noveon agreed that it was appropriate to resolve the ammonia issue raised in the
permit appeal by pursuing adjusted standard relief from the Board.
35 ILL.
ADM.
CODE 104.406 INFORMATIONAL REQUIREMENTS
I.
Standard From Which Relief Is Sought
--
Section 104.406(a)
Noveon does not believe that, for the reasons discussed earlier in this petition, 35 Ill.
Adm. Code 304.122(b), effective 1972, is applicable to its wastewater discharge from the Henry
Plant. Nonetheless, to resolve this issue with the Agency Noveon agreed to seek an adjusted
standard from the ammonia effluent limit of35 Ill. Adm. Code 304.122(b).
II.
Nature of Regulation ofGeneral Applicability
--
Section 104.406(b)
A. Ammonia Effluent Limitations
On January 6, 1972, the Board adopted Rule 406 ofits water pollution rules, which
limited the ammonia nitrogen level ofcertain dischargers to the Illinois River. That rule has
since been amended and is now codified at 35 Ill. Adm. Code 304.122. The rule as promulgated
was specifically intended to reduce the discharge of ammonia nitrogen to the Illinois River from
4
limit, 35 Ill. Adm. Code 304.122 remained in the Board’s regulations as ammonia nitrogen
effluent limitations.
B. Ammonia
Water
Quality
Standards
Noveon recognizes that as part ofthe triennial review ofwater quality standards the
Agency performs under Section 303(c)(1) ofthe Clean Water Act, 33 U.S.C.
§
1313(c)(1),
significant amendments to the water quality standards for ammonia nitrogen were adopted by the
Board toward the end ofthe 1996. In the Matter of: Triennial Water Quality Review
Amendments, R94-1(B) (Dec. 19, 1996) (Final Order). As amended in 1996, the ammonia water
quality standards consist offour separate un-ionized ammonia standards: an acute summer
standard, a chronic summer standard, an acute winter standard and a chronic winter standard. 35
Ill. Adm. Code 302.2 12. The ammonia nitrogen water quality standards, as amended, have been
approved by the U.S. EPA.
Noveon is also aware that the Board currently has pending before it a proposal to amend
again the ammonia water quality standards. The proposed amendments, if adopted, will change
the acute and general use water quality standards for un-ionized ammonia, among other proposed
changes to the ammonia water quality standards. Noveon is not seeking an adjusted standard
from the ammonia water quality standards, because as discussed below, Noveon meets those
standards through use ofa ZID and a mixing zone.
C. Mixing Zone and ZID
With an appropriately calculated zone of initial dilution (“ZID”) and mixing zone,
consistent with both Agency and U.S. EPA guidance on mixing zones, the discharge from the
Henry Plant will meet the summer/winter acute and chronic limitations set forth in the amended
ammonia water quality standards. See Exhibit 1. In Illinois water quality standards must be met
6
at the 7Q10 low flow condition. Historical river data has been analyzed by Noveon from various
monitoring stations, including the Agency’s Hennepin, IL and United States Geological Survey
(“USGS”) Henry, IL monitoring stations to determine appropriate ambient river parameters to
determine an appropriate mixing zone. See Exhibit 2.
Field studies have been conducted on the Henry Plant’s discharge to analyze the in-river
mixing taking place. According to the analysis arising from those field studies, based on a
computed total cross-sectional area, and a maximum plume width of 160 feet in the river, the
effluent plume will require less than 18 ofthe cross-sectional area ofthe total 875 foot width
ofthe Illinois River in the vicinity ofthe Henry Plant for a mixing zone. In addition, the 26-acre
limitation on mixing zones is easily met by the discharge from the Henry Plant. The size ofthe
ZTD calculated by Noveon’s consultant is
66.5
feet, with a mixing zone ofa 1,000 feet. See
Exhibit 1. This ZID and mixing zone will allow the effluent from the Henry Plant to meet both
the summer (April through October) and winter (November through March) acute and chronic
water quality standards at total ammonia nitrogen effluent discharge limits ofno greater than
189 mg/L for winter and for summer. See Exhibit 3 at Figure 1.
To ensure that maximum mixing continues to occur sufficient to meet the acute and
chronic ammonia water quality standards, Noveon will agree to replace the current single-port
diffuser with a multi-port diffuser, as part ofthe relief in this proceeding. Specifically, Noveon
will install and maintain a high-rate multi-port diffuser that will immediately and rapidly
disperse the treated effluent from Noveon into the Illinois River within a short distance from the
diffuser (on the order ofone diffuser length). The diffuser will be at least 15 ft. long and will be
placed in the river so that the normal water depth over the diffuser will be about 13 ft. at low
pool elevation of440 feet above the National Geodetic Vertical Datum of 1929. There will be
7
rime 2-in, ports set at an angle of 60 from horizontal, and the ports will be co-flowing with the
river. The port exit velocities have been designed to achieve an exit velocity of 10 fi/sec, which
will prevent habitation by biological species in the immediate vicinity ofthe diffuser. The
diffuser has been designed, using accepted U.S. EPA diffuser models, to meet an effluent
dispersion of43:1 for an effluent flow of 1.3 mgd, and all water quality parameters will be met at
the edge ofthe zone ofinitial dilution. The multi-port diffuser will be installed within a year of
the granting by the Board ofthe adjusted standard requested herein. See Exhibit 3 for a detailed
description of the multi-port diffuser.
Consequently, Noveon is not seeking adjusted standard relief from the ammonia water
quality standards. Noveon is only seeking an adjusted standard from the ammonia effluent limit
for discharges into the Illinois River as set forth in 35 Ill. Adm. Code 304.122(b). Noveon also
seeks from the Board as part ofthis proceeding, a determination that the ammonia water quality
standards will be met with the ZD and mixing zone calculated in Exhibit 1 and 3 and as
discussed above for the Henry Plant discharge.
III.
Specified Level of Justification
—
Section 104.406(c)
The regulation of general applicability from which Noveon seeks an adjusted standard
does not specify a level ofjustification. Thus, the Board can grant the adjusted standard upon
adequate evidence ofthe four criterion set forth in Section 28.1(c) ofthe Act, along with the
information required by 35 Ill. Adm. Code 104.406. The four criterion required by Section
28.1(c) ofthe Act are discussed later in this petition.
8
IV.
Facility and Process Description
--
Section 104.406(d)
A. Facility and Process Description
The HenryPlant is located on 1550 County Road, 850 N., in Henry, Illinois in
northwestern Marshall County. The facility was solely owned and operated by the BFGoodrich
Company from its initial construction in 1958 until 1993. In 1993, the BFGoodrich Company
divested the Geon Vinyl Division from the company and formed The Geon Company (“Geon”),
a separate, publicly held company. In February 2001 the BFGoodrich Company sold all the
assets of its chemical business, including the Henry Plant, and that former BFGoodrich division
is now known as Noveon, Inc.
Today, both Geon (now known as PolyOne) and Noveon continue to operate facilities at
the Henry site. The wastewater treatment system is owned and operated by Noveon, and the
system continues to treat the wastewater from both PolyOne’s and Noveon’s Henry Plant
processes. Approximately 360,000 gallons per day ofeffluent from the PolyOne operations are
treated by the Henry Plant wastewater treatment system and the Noveon operations contribute
approximately 180,000 gallons per day. The total daily discharge ofprocess water and non-
process water is approximately 800,000 gallons from the Henry Plant’s wastewater treatment
system. Noveon currently employs approximately 85 people and the PolyOne facility employs
approximately 100 people at the site.
The Noveon Henry Plant produces rubber accelerators and antioxidants for the rubber,
lubricant and plastic industries. The rubber accelerators are used in tires and other rubber goods
to “accelerate” the curing process. The antioxidants are used to inhibit the oxidation process in
materials such as rubber, jet fuel, greases, oils and polypropylene.
9
In the production of accelerators there are several key raw materials: sulfur, aniline,
carbon disulfide and amines. The manufacture ofaccelerators is a multi-step process including
the manufacture of an intermediate (sodium mercaptobenzothiazole). This intermediate is then
reacted with an amine and other raw materials to form an accelerator product. The product is
then isolated through filtration and drying.
There are various types ofantioxidants manufactured by Noveon at the Henry Plant. In
general, the antioxidant processes utilize either diphenylamine or one ofseveral phenols as a
starting material. The processes in which these products are manufactured consist ofboth batch-
and continuous reactors, filtration operations and solidification.
PolyOne produces polyvinyl chloride (“PVC”) resins. These resins are sold to a variety
ofcustomers including those in the construction, household furnishings, consumer goods,
electrical, packaging and transportation industries. While PolyOne is not a party to this
proceeding, as noted earlier, its process wastewater is combined with the Noveon wastewater and
treated in the Henry Plant’s wastewater treatment system by Noveon.
Between 1985 and 1987, three major physical changes occurred at the Henry Plant. The
first involved the installation ofa fluidized bed coal-fired boiler, which became operational in
1985, and is now operated by PolyOne. The second involved the addition offacilities for a new
rubber accelerator process building that became operational in 1986. In 1987 Noveon
significantly upgraded its wastewatertreatment system. This upgrade included installation of
two above ground biotreators, two above ground equalization tanks and a tertiary filtration
system. A third biotreator was added in 1989 and a fourth one was placed into service in 1998.
Auxiliary equipment and pretreatment systems were also installed to facilitate the operation and
effectiveness ofthe wastewater treatment system.
10
The levels of ammonia in the Henry Plant’s wastewater were particularly puzzling and
iequired significant investigation to discover the source, since ammonia is not a major raw
material in any ofthe processes at either PolyOne or the Noveon Henry Plant. As an ingredient
in the production processes, ammonia is only used in minor amounts in one low volume product
manufactured by Noveon at the Henry Plant. The only other ammonia used by Noveon at the
Henry Plant is in the ammonia cooling system, which utilizes ammonia in a closed-loop system
from which no ammonia is released. PolyOne uses a small amount of ammonia as an ingredient
to produce an emulsifier foruse in one ofthe PVC processes. Ammonia, however, is not a
primary ingredient in any ofthe processes carried out by either Noveon orPolyOne nor in the
products either company produces.
Since ammonia is not used in any significant amount in the processes conducted by either
Noveon or PolyOne that ultimately discharge to the Henry Plant’s wastewater treatment plant,
the levels of ammonia in the effluent required extensive investigation and analyses to determine
why ammonia was in the effluent following treatment. As discussed later in this petition, it was
ultimately discovered that the major source ofammonia is the degradation of amines that occurs
in the wastewater treatment process at the Henry Plant. The efforts ofNoveon to address the
source ofthe ammonia is also fully discussed later in this petition.
B. The Henry Plant Wastewater Treatment
System
The wastewater treatment system at the Henry Plant is a multi-process system that treats
both process wastewater and non-process discharges including stormwater and non-contact
cooling water. A block flow diagram of the system is included as Exhibit 4. The Henry
wastewater treatment system has historically provided greater than
95
BOD reduction while
11
discharging ammonia-nitrogen in an effluent concentration range of23 mg/L to 150 mg/L. See
Exhibit
5
and Exhibit 6 at 1-1.
Pretreatment ofcertain process wastewaters is the initial step in the treatment process.
The Cure-Rite 1 8® wastewater is pretreated with hydrogen peroxide. Some ofthe PVC
wastewater from PolyOne is pretreated by a wastewater stripping system that removes residual
vinyl chloride. PolyOne also pretreats certain centrate waste streams prior to discharge to the
Henry Plant’s wastewater treatment system.
Following pretreatment, all process wastewater is collected in equalization tanks prior to
transfer to the primary treatment system. Wastewater from the Henry Plant’s production of
accelerators and antioxidants discharge to either the polymer chemicals (“PC”) equalization tank
or to the Cure-Rite 1 8® equalization tank. PolyOne’s wastewater and sidestreams from the
combined wastewatertreatment facility discharge to the PVC equalization tank. Site-wide
stormwater runoffand sidestreams from the boilerhouse and water treatment facility discharge to
two holding ponds.
In the primary treatment system, the wastewater is fed into the treatment process where
pH is adjusted, coagulants are added, and a large settleable floc, a cluster of particles, is formed.
The wastewater is then sent to the primary clarifierwhere the solids in the wastewater settle to
the bottom. The solids that settle in the primary clarifier are pumped into a collection tank and
processed through a filter press for dewatering before being sent off-site to a landfill as a non-
hazardous special waste. The wastewater collected from the filter press is recycled back into the
treatment system.
After primary clarification, the wastewater is sent to activated sludge treatment by the
biotreatmnent system consisting offour “biotreators.” The biotreators are tanks that range in size
12
from 400,000 gal. to 1.3 million gal. and contain biomass to degrade the organic matter in the
wastewater. The degradation process is augmented by the addition of air into the biotreators.
The addition of air into the biotreators ensures that the biomass has sufficient oxygen to
complete the degradation oforganic materials and also ensures through agitation that the
biomass comes into adequate contact with the organic matter contained in the wastewater.
After biological treatment in the biotreators, the wastewater flows into the secondary
clarifier where more coagulants are added. The solids removed during secondary clarification
are primarily biomass and are returned to the biotreators.
The wastewater from the secondary clarifier is then sent to tertiary treatment provided by
a polishing filtration device called a traveling bridge sand filter. As the wastewater passes
through the sand bed, additional solids removal occurs and the effluent flows into a concrete
sump leading to the outfall. Any backwash from the sand filter is recycled back into the primary
treatment system and is processed again.
-
The non-process wastewater, including non-contact cooling water, stormwater, water
from the boilerhouse demineralizer and water treatment works, is discharged to a holding pond.
The non-process wastewater is then either pumped into the primary treatment system or pumped
directly to the sand filter to remove solids prior to discharge through the outfall.
The City ofHenry operates a municipal wastewater treatment system adjacent to the
Henry Plant and also contributes flow to the Henry Plant’s outfall. The City ofHenry municipal
treatment system consists ofan aerated lagoon followed by a sedimentation basin and effluent
disinfection. The treated discharge from the City ofHemy municipal wastewater treatment
system combines with the treated Henry Plant effluent and is discharged together through the
Henry Plant’s outfall into the Illinois River. Compliance sampling ofthe Henry Plant and City
-
13
ofHenry waste streams is performed before the waste streams are combined. It also should be
noted that the Agency has determined that the Henry Plant wastewater treatment system achieves
“best degree oftreatment” for all pollutants except for ammonia.
C. Description ofArea Affected
Following treatment, the wastewater is discharged through Outfall 001 to the Illinois
Riverpursuant to NPDES Permit No. IL0001392. The Illinois River is formed at the junction of
the Kankakee and Des Plaines Rivers near Joliet, Illinois and runs 273 miles west, southeast and
south to the Mississippi River, near Grafton, Illinois, which is a few miles upstream from St.
Louis. The Henry Plant is located on the right edge ofthe water (when looking downstream)
betweenriver mile 198 and 199.
The Illinois River at Henry is approximately 875 feet wide, with an approximate 18 foot
maximum depth. The average depth ofthe river is 11 feet, and it has a drainage area of
approximately 13,543 square miles at Henry, IL. The USGS has operated a gauging station at
Henry, Illinois since October 1981. The available USGS data for this gage indicate that the
Illinois River at this location has an annual mean flow of 15,340 cfs. The Illinois State Water
Survey reports an annual 7-day, 10-year low flow for the river at Henry of3,400 cfs.
D. Description ofDischarge
The effluent from the Henry Plant is discharged through an 18-inch, single-port
submerged diffuser into the main channel ofthe Illinois River. Since the Henry Plant sits 40 to
50 feet above the Illinois River, the effluent enters the river with a great deal ofvelocity. This
velocity causes rapid and immediate mixing, resulting in maximum effluent concentration
reductions and is ofsufficient turbulence to discourage habitation by aquatic organisms in the
14
areaofthe diffuser. As mentioned earlier, Noveon will agree to replace the current single-port
diffuser with a multi-port diffuser, as part ofthe relief in this proceeding.
The effluent from the HenryPlant historically has had an ammonia nitrogen
concentration ranging from 23 to 150 mg!L. See Exhibit
5
and Exhibit 6 at 1-1. Based on an
analysis ofthe Henry Plant discharge, up to 189 mg/L total ammonia can be discharged from the
existing single-port diffuser during summer and winter conditions, respectively, and still achieve
the applicable acute and chronic ammonia water quality standards. See Exhibit 3 at Figure 1.
The replacement ofthe single-port diffuser with a multi-port diffuser will ensure that the
discharge from the Noveon Henry Plant continues to meet applicable water quality standards.
Exhibit
5
contains the most recent summary ofthe types and quantities of other substances
present in the treated Henry Plant effluent.
Over the years Noveon expended significant resources in evaluating its production
processes and wastewater treatment system in an effort to determine what was contributing to the
ammonia levels in its wastewater. As noted earlier, the levels did not correspond to the small
amount ofammonia used by Noveon or PolyOne in theirrespective processes. As a result ofthe
various studies conducted by and on behalfofNoveon, it has been determined that ammonia is
generated as a degradation product of the Henry Plant’s wastewater treatment system. In
particular, the degradation ofamines in the wastewatertreatment process produces the ammonia
found in Noveon’s effluent. The efforts ofNoveon to evaluate various compliance alternatives
are discussed in the next section ofthis petition.
V.
Cost of Compliance and Compliance Alternatives
--
Section 104.406(e)
As detailed below, Noveon has examined a variety of methods to reduce the level of
ammonia in its effluent. Initially, the Henry Plant evaluated the existing treatment system’s
15
ability to nitrif~’,or oxidize ammonia to nitrates. These preliminary nitrification studies led
Noveon to retain Brown and Caldwell, flk/a EckenfelderInc., to perform treatability studies
concerning the ability ofthe Henry Plant to nitrif~’.The proposal for the Brown and Caidwell
nitrification work was shared with the Agency, and the Agency’s comments and suggestions
resulted in a revisedproposal to examine the potential ofthe Henry Plant to operate as a single-
stage nitrifying unit.
-
Noveon originally had Brown and Caldwell examine the ability to reduce ammonia
through single-state biological nitrification in the late 1980’s. This early study concluded that
single-stage biological nitrification was not achievable in the existing activated sludge system.
The Agency requested a more extensive study ofsingle-stage nitrification as a means to reduce
ammonia. The requested additional treatability study was completed in December
1995,
and a
report was prepared and submitted to the Agency. The results ofthe treatability study
conclusively demonstrated that the Henry Plant could not achieve single-stage nitrification under
existing waste loads and optimum conditions ofmixed liquor pH, D.O., temperature, alkalinity,
F/M ratio and mean cell residency time. See Exhibit 6 at 1-1. The study also showed that the
addition ofa commercially provided “nitrifier-rich” biomass to the wastewater treatment plant
would not prompt the initiation ofnitrification due to the wasteload characteristics and not the
operating conditions. The inability of the Henry Plant wastewater treatment system to nitrify
was due to inhibition ofnitrifying bacteria by the PC tank and C-18 tank contents flows.
Noveon did not simply stop its efforts toward finding a solution for the ammonia issue
once it was determined that nitrification would not work. Noveon has investigated various other
technologies for the control andlor reduction ofammonia in its discharge. In general, Noveon
examined three areas for institution ofpossible technology-based ammonia reduction measures:
16
1) in-process reductions; 2) pretreatment ofthe wastestream; and 3) post-treatment ofthe
wastestream. The options that Noveon explored in each ofthese three categories are discussed
below.
A. In-Process Reductions
Noveon explored whether it could eliminate the use ofamines in the various processes or
whether it could recover andlor recycle the precursors to ammonia for reuse in the system. Both
ofthese methods were rejected as feasible compliance alternatives following analysis by a
research and development team from Noveon. Amines are an essential element in many of the
products that Noveon produces at the Henry Plant, and elimination of amines would essentially
require the complete elimination ofthe affected product lines, if not closing the entire plant. The
recycling option was also rejected on the basis that the recycled material was ofinferior quality
and would not guarantee production ofthe standard, high quality product Noveon’s customers
demand. In addition, the waste material generated in the recycling process would likely be
classified as a hazardous waste, which raises concerns about cross-mediaimpact associated with
this alternative. Excess amines are, however, currently recovered from processes where recovery
methods provide reusable quality materials and are not cost prohibitive.
B. Pretreatment
The second option, additional pretreatment of the wastewater, involved the removal of
certain constituents before the water was sent to the wastewater treatment system. Noveon
investigated a variety ofpretreatment options, including morpholine recovery, TBA recovery and
a liquid extraction process in which a solvent is passed counter-current to the wastewater
removing the amines from the water. None ofthe pretreatment options would achieve reduction
that would result in compliance with the ammonia effluent standard of35 Ill. Adm. Code
17
304.122(b). The pretreatment options also raised various technical issues including plant
personnel safety issues.
-
C. Post-treatment
Once it became clear that the Henry Plant could not achieve compliance through single-
stage nitrification, in process reductions or pretreatment options Noveon retained Brown and
Caldwell to develop preliminaryprocess designs and cost estimates to evaluate other post-
treatment alternatives that could reduce the ammonia in the effluent from the Henry Plant. The
report prepared by Brown and Caldwell is attached as Exhibit 6.
The alternatives consideredby Brown and Caldwell included:
1.
Alkaline air stripping at different points in the wastewater treatment system (e.g.,
PC tank, PVC tank and secondary clarifier).
2.
Struvite precipitation from the combined wastestream influent.
3.
Effluent breakpoint chlorination.
4.
Single-stage biological nitrification of non-PC wastestream combined with
separate biological treatment ofthe PC tank discharge.
-
5.
Biological nitrification ofcombined influent wastestream.
6.
Ion exchange treatment offinal effluent.
Ozonation and tertiarynitrification are two other potential compliance alternatives evaluated
after Brown and Caldwell completed the evaluation of compliance alternatives discussed in
Exhibit 6. Each ofthese post-treatment alternatives that were evaluated and the conclusions
reached by Brown and Caldwell are summarized below. Flow diagrams of each these ammonia
reduction alternatives are included in the figures to Exhibit 6 and in Attachment A to Exhibit 7.
18
1.
Alkaline Air Stripping
Ammonia exists in two forms, aqueous and gaseous, and as pH increases the aqueous
form becomes a gas. Thus, by increasing the pH of a wastewater stream it is possible to strip or
remove the ammonia gas. This alternative as investigated involved the use ofair stripping at
three separate portions ofthe treatment system as a means of ammonia removal: 1) within the
PC tank; 2) within the PVC tank and 3) the secondary clarifier effluent. See Exhibit 6 at 2-1 to
2-2.
Because samples of the PC tank and PVC tank discharges contained greater than 500
mg/L TSS, a packed tower air stripper or horizontal tray stripper would require frequent
maintenance due to fouling. Thus, diffused air stripping and surface aeration processes were
both selected for evaluation in both the PC tank and PVC tank. Due to the slow rate of these
stripping processes, the small amount ofammonia available in these tanks, and the large flow
rates ofthe wastewater into the PC tank and PVC tank, only stripping within existing tankage
was considered. Building additional tankage and aeration equipment to address ammonia
removal from these wastestreams would have offered little additional benefit since the bulk of
the ammonia discharged from the Henry Plant is generated as a by-product in the downstream
wastewater treatment facility. Conventional packed tower air stripping was selected for
evaluation of the wastewater treatment facility effluent downstream ofthe secondary clarifier
wastewater since this is a well-established stripping technology.
The batch air stripping test results from 1996 for the PC tank, PVC tank and secondary
clarifier wastewater indicated that some ammonia reduction in those wastestreams could be
achieved. A combined removal ofammonia from the wastewater, however, ofless than 20
would be achieved by treatment ofeither the PC tank or PVC tank wastewater using surface
19
aeration stripping technology. See Exhibit 6 at 2-1 to 2-2. This low level ofammonia reduction
means air stripping from the PC tank and PVC tank would not achieve sufficient ammonia
reduction that would allow the Henry Plant meet the effluent limitation of35 Iii. Adm. Code
304.122(b). Further, given the presentworth costs (capital, operation and maintenance costs) of
$2.3 million for PC tank treatment and $14.1 millionfor PVC tank treatment, this alternative was
also deemed economically unreasonable in light ofthe high costs and low ammonia reduction
obtained. See Exhibit 7 at pgs. 2-3.
The ammonia removal achieved from the secondary clarifier was greater than 95 using
packed tower air stripping technology. This technology was evaluated again in 2000. One
difficulty with this alternative is that it would increase TDS by more than 20, which could lead
to aquatic toxicity ofthe effluent. The most important difficulty with this treatment alternative is
its high operation, maintenance and installation costs, which makes it an economically
unreasonable one with present worth costs ofover $14 million. See Exhibit 7 at pgs. 2-3. The
costs associated with this alternative are so high because additional equipment is required to
remove the ammonia from the off-gases.
2.
Struvite Precipitation
This alternative involved an analysis ofthe ammonia reduction achieved by the
precipitation ofstruvite (NH4MgPO4.6H2O) from the combined Noveon Henry Plant and
PolyOne wastestream. See Exhibit 6 at 2-2 to 2-4. The results ofthe batch treatability studies
indicate that under certain operating conditions the combined wastestream ammonia
concentration can be reduced to approximately 25 mg/L in the treatment plant influent. This
treatment process, however, would provide only a 24 reduction in the average final
effluent
20
ammonia level at a present worth cost of
$5.1
million. See Exhibit 7 at 2-3. This alternative also
would increase TDS in the Henry Plant effluent.
In sum, struvite precipitation would not result in compliance with the ammonia effluent
limit. Because only a small portion of the wastewater nitrogen load would be removed from the
Henry Plant treatment system by struvite precipitation, combined with its high costs, this is not a
feasible compliance alternative.
3.
Effluent Breakpoint Chlorination
Brown and Caldwell also evaluated the use ofchlorine to achieve ammonia reduction.
This alternative involved gravity discharge ofthe secondary clarifier wastewater to a reaction
tank where chlorine gas would be sparged into the tank and caustic soda added to maintain a pH
of approximately 6.9. See Exhibit 6 at 3-3 to 3-4. Following the addition ofchlorine, the
wastewaterwould be discharged to the existing sand filters.
This alternative could meet the ammonia standard set forth in 35 Ill. Adm. Code
304.122(b). See Exhibit 6 at 3-4. The problem it presents, however, is that breakpoint
chlorination is prohibitively expensive, at a present worth cost of$9.7 million, which makes it
economically unreasonable. See Exhibit 7 at pgs. 2-3. Thus, this alternative is economically
unreasonable. This alternative will also dramatically increase effluent TDS and may likely result
in the formation of chlorinated organics in the effluent.
4.
Single-stage Biological Nitrification ofNon-PC Wastewater
Noveon’s consultant also examined what level of ammonia reduction would occur by
first-stage nitrification ofthe non-PC wastewater followed by second-stage biological treatment
ofthe PC tank wastewater after combination with effluent from the first-stage reactor. It was
determined afterthe batch treatability study that this was not a feasible compliance alternative
21
because ofthe low level of ammonia reduction that was achieved. The percentage of ammonia
reduction was only 47 and yet had a present worth cost of$4.9 million. See Exhibit 6 at 2-4 to
2-7 and Exhibit 7 at pgs. 2-3.
5.
Biological Nitmification ofCombined Wastewater
This alternative required pH reduction to 2 ofthe PC tank discharge, followed by river
water addition and combined single-stage nitrification with non-PC wastestreams. The results of
the analysis by Noveon’s consultant, Brown and Caldwell, showed that biological nitrification of
the combined wastewater stream was a technically feasible compliance alternative. See
Exhibit 6 at 4-1. This alternative suffers from a lack ofreliability, which is necessary for
consistent compliance, since it is sensitive to the variable characteristics inherent in the
wastewater produced by the different batch processes at the Henry Plant.
Further, biological nitrification is a very costly alternative. Brown and Caldwell
estimated that the present worth costs ofthis alternative at $11.7 million. See Exhibit 7 at pgs. 2-
3. Those costs make this an economically unreasonable alternative, particularly in light of the
reliability concerns associated with it.
6.
Ion Exchange
One other compliance alternative analyzed by Brown and Caidwell was ion exchange
treatment ofthe secondary clarifier effluent using clinoptilolite, an ammonia selective ion
exchange resin. See Exhibit 6 at 2-9 to 2-10; 3-4. This alternative could meet the ammonia
effluent standard of 35 Ill. Adm. Code 304.122(b). The batch treatability test results
demonstrated that approximately 50 lbs. ofclinoptilolite would be required to remove each
pound of ammonia. This poor removal efficiency was presumed to be due to the large
concentration ofcompeting ions in the effluent. Id. at 3-4. The poor selectivity of this
22
alternative for removing ammonia precluded further consideration ofion exchange as a
compliance alternative. This alternative had a present worth cost of$5.1 million. See Exhibit 7
at pgs. 2-3.
7.
Ozonotion
This ammonia treatment alternative was evaluated recently by Noveon’s consultant as a
compliance alternative. This alternative could meet the ammonia standard set forth in 35 Ill.
Adm. Code 304.122(b). It was rejected as an alternative due to its high present worth costs of
$20.3 million. See Exhibit 7 at pgs. 2-3. Further, it would significantly increase the effluent
TDS concentrations. This alternative would likely also convert some ofthe effluent non-
degradable COD into BOD, which could cause BOD effluent limit violations.
8.
Tertiary Nitrification
This alternative would involve pumping the secondary clarifier effluent through a
separate aeration basin containing fixed film media that nitrifying bacteria would grow on.
Alkalinity and D.O. would be controlled in this basin to meet the demands associated with
nitrification. Effluent from this tank would be directed to the existing tertiary filtration process
that would be expanded to accommodate the additional solids loading. Results ofanalyses dating
back to the late 1980s and confirmed during the 1990s indicate this process is a technically
feasible compliance alternative. The difficulty with this alternative is that it lacks reliability,
which is necessary to achieve compliance, due to its great sensitivity to variations in wastewater
characteristics that occur with the Henry Plant’s batch processes.
Further, tertiary nitrification is a very costly alternative. Brown and Caldwell estimated
that the present worth costs oftertiary nitrification is $11.4 million. See Exhibit 7 at pgs. 2-3.
23
Those costs make this an economicallyunreasonable alternative, particularly in light ofthe
reliability concerns associated with it.
In sum, Noveon evaluated a number ofin-process reductions, pretreatment measures and
post-treatment measures as methods to achieve compliance with the effluent limits of35 Ill.
Adm. Code 304.122. The results ofits evaluation demonstrate that there is no alternative that is
both technically feasible and economically reasonable that would allow the Hemy Plant to
achieve compliance with the ammonia effluent limit of35 Ill. Adm. Code 304.122(b).
VI.
Proposed Adjusted Standard
--
Section
104.406(1)
Noveon proposes the adoption by the Board of one of the following alternatives as the
adjusted standard language:
Alternative #1
Noveon, Inc. (“Noveon”) is hereby granted an adjusted standard
from 35 Ill. Adm. Code 304.122. Pursuant to thisadjusted
standard, 35 Iii. Adm. Code 304.122 shall not apply to the
discharge of effluent into the Illinois River from the Noveon plant
located at 1550 County Road, 850 N., in Henry, Illinois as regards
ammonia nitrogen. The granting ofthis adjusted standard is
contingent upon the following conditions:
A.
Noveon shall not discharge calculated un-ionized ammonia at
concentrations greater than
3.5
mg/l during the months of
April through October and 7.9 mg/l during the months of
November through March from its Henry, Illinois plant into
the Illinois River.
B.
Discharge into the Illinois River shall occur through a
diffuser that is at least 15 ft. in length, with 9 two-inch ports,
angled at 60 degrees from horizontal, co-flowing with the
river, designed to achieve an effluent dispersion of43:1.
Alternative #2
Noveon, Inc. (“Noveon”) is hereby granted an adjusted standard
from 35 Ill. Adm. Code 304.122. Pursuant to this adjusted
standard, 35 Ill. Adm. Code 304.122 shall not apply to the
24
discharge ofeffluent into the Illinois River from the Noveon plant
located at 1550 County Road, 850 N., in Henry, Illinois as regards
ammonia nitrogen. The granting ofthis adjusted standard is
contingent upon the following conditions:
A.
The water quality standards will be met by the Noveon
Henry plant limiting its total ammonia nitrogen discharge
to 1200 pounds per day during the months ofApril through
October and 1735 pounds per day during the months of
November through March.
B.
Discharge into the Illinois River shall occur through a
diffuser that is at least 15 ft. in length, with 9 two-inch ports,
angled at 60 degrees from horizontal, co-flowing with the
river, designed to achieve an effluent dispersion of43:1.
Alternative #3
Noveon, Inc. (“Noveon”) is hereby granted an adjusted standard
from
35
Ill. Adm. Code 304.122. Pursuant to this adjusted
standard,
35
Ill. Adm. Code 304.122 shall not apply to the
discharge ofeffluent into the Illinois River from the Noveon plant
located at 1550 County Road, 850 N., in Henry, Illinois as regards
ammonia nitrogen. The granting ofthis adjusted standard is
contingent upon the following conditions:
A.
Noveon shall not discharge total ammonia nitrogen at
concentrations greater than
155
mgll during the months of
April through October and 225 mg/l during the months of
November through March from its Henry, Illinois plant into
the Illinois River.
B.
Discharge into the Illinois River shall occur through a
diffuser that is at least 15
ft.
in length, with 9 two-inch ports,
angled at 60 degrees from horizontal, co-flowing with the
river, designed to achieve an effluent dispersion of 43:1.
VII.
Environmental Impact
--
Section 104.406(g)
The granting ofthe adjusted standard will not result in any adverse environmental impact.
As noted earlier, the Board’s rationale at the time
35
Ill. Adm. Code 304.122 was adopted was
premised upon the belief that larger dischargers were contributing to D.O. sags. The study
underlying that belief was later refuted by its authors when it was discovered that the D.O. sags
25
were occurring not as a result oflarger dischargers but primarily because ofsediment oxygen
demand. The discharge from the Henry Plant will not have a measurable effect on the D.O. in
the Illinois River.
Further, under the Board’s mixing zone regulations, it is appropriate to allow the mixing
of effluent with the receiving stream before determining compliance with water quality
standards. See, e.g., 35 Ill. Adm. Code 302.102. No adverse environmental impact will occur
because at the edge ofthe ZID and mixing zone calculated by Noveon’s consultant, consistent
with Agency and U.S. EPA guidance, both the winter (November through March) and summer
(April through October) acute and chronic water quality standards for ammonia will be readily
met. See Section II C. ofthis Petition.
The regulations set forth at 35 Ill. Adm. Code 302.102 govern allowed mixing, mixing
zones and zones of initial dilution. The calculated ZID and mixing zone proposed as a part of
this adjusted standard will meet each ofthe requirements of35 Ill. Adm. Code 302.102(b), in
that:
-
A.
Mixing will be confined in an area or volume ofthe Illinois River no
larger than the area orvolume which would result afterincorporation of
a multi-port diffuser, engineered location and configuration ofdischarge
points to attain optimal mixing efficiency ofeffluent and the Illinois
River.
B.
Mixing will not occlude any tributary mouth or otherwise restrict the
movement ofaquatic life into or out of the tributary.
C.
-
Mixing will not occur in waters adjacent to bathing beaches, bank
fishing areas, boat ramps ordockages, or any other public areas.
D.
Mixing will not occur in waters containing mussel beds, endangered
species habitat, fish spawning areas, areas ofimportant aquatic life
habitat, or any other natural features vital to the well being ofaquatic
life in such a manner that the maintenance of aquatic life in the body of
water as a whole is adversely affected.
26
E.
Mixing will not occur in waters which contain intake structures of
public or food processing water supplies, points ofwithdrawal ofwater
for irrigation, or watering areas accessed by wild or domestic animals.
F.
Mixing will allow for a zone of passage for aquatic life in which water
quality standards are met.
G.
The areaand volume in which mixing occurs, alone or in combination
with other areas and volumes ofmixing, will not intersect any area or
volume ofany body ofwater in such a manner that the maintenance of
aquatic life in the body ofwater as a whole is adversely affected.
H.
The area and volume in which mixing occurs, alone or in combination
with other areas and volumes ofmixing, will not contain more than 25
percent ofthe cross-sectional area or volume offlow ofthe Illinois
Riverincluding areas where the dilution ratio is less than 3:1. Mixing
will not occur in an area ofthe Illinois River having a zero minimum
7Q10.
I.
Mixing will not occur where the water quality standard for ammonia is
already violated in the Illinois River.
J.
The total Illinois River flow is not used for mixing.
K.
The source ofeffluent is limited to a total area and volume ofmixing no
larger than that allowable for a single outfall.
L.
The area and volume in which mixing will occur is as small as is
practicable under the limitations prescribed in 35 Ill. Adm. Code
302.102, and in no circumstances does the mixing encompass a surface
area larger than 26 acres.
Thus no adverse environmental impact, including harm to aquatic life, will result from the
granting ofthe requested adjusted standard, and the mixing, zone ofinitial dilution and mixing
zone that are an integral part ofthe relief Noveon seeks meet the requirements of 35 Iii. Adm.
Code 302.102.
VIII. Justification for Adjusted Standard
—
104.406(h)
As noted previously, the regulation of general applicability from which Noveen seeks an
adjusted standard does not specify a level ofjustification for such a standard. Section 28.1(c) of
27
the Act, however, allows the Board to grant an adjusted standard in the absence ofa specified
level ofjustification if the Board determines based upon adequate proofby the petitioner that:
A.
Factors relating to the petitioner are substantially different from the
factors relied upon by the Board in adopting the general regulation;
B.
The existence ofthose factors justifies an adjusted standard;
C.
The requested standard will not result in environmental or health effects
substantially and significantly more adverse than the effects considered
by the Board in adopting the rule ofgeneral applicability; and
D.
The adjusted standard is consistent with federal law.
415 ILCS
5/28.1(c).
Each ofthese factors is discussed below.
1.
Substantially Different Factors
--
Section 28.1(c)(1)
The existing ammonia effluent regulation in 35 Ill. Adm. Code 304.122 is premised upon
two factors: the ability to treat ammonia and the desire to address D.O. concerns in the Illinois
River. Regarding the ability to treat ammonia, in amending the generally applicable rule the
Board expressly noted that “present technology is capable ofmeeting this limit and should result
in the removal ofmuch ammonia nitrification oxygen demand
...
from these stressed
waterways.” In the Matter ofWater Quality Standards Revisions, R72-4 (Nov. 8, 1973) (Final
Opinion). In general, there is technology capable of meeting the ammonia nitrogen limitation set
forth in 35 Ill. Adm. Code 304.122. Specifically as applied to the Henry Plant wastewater,
however, the numerous investigations and studies conducted by and on behalf ofNoveonhave
established that there are no alternatives that are both technologically feasible and economically
reasonable to achieve the ammonia reduction necessary to comply with 35 Ill. Adm. Code
304.122(b).
28
Secondly, the underlying technical justification that led the Board to adopt the general
rule, a concern about D.O. sags in, among other rivers, the Illinois River was later refuted as
being caused primarily by the discharge ofammonia nitrogen. Rather, the D.O. sags were later
determined to be primarily caused by sediment oxygen demand. Ammonia discharged at the
level requested by Noveon will thus have minimal, if any, impact upon the level of D.O. in the
Illinois River. See Exhibit 2. Nor will it contribute to any water quality violations or harm to
aquatic life as discussed in Section VII. above. In sum, the factors relied upon by the Board in
adopting what is now 35 Iii. Adm. Code 304.122 were substantially different than those
applicable to the Noveon HenryPlant.
2.
Adjusted Standard Justification
--
Section 28.1(c)(2)
One factor that must be taken into consideration when adopting environmental
regulations in the State ofIllinois is economic reasonableness. 415 ILCS 5/27. The ammonia
nitrogen effluent limit from which Noveon seeks relief was adopted based upon balancing the
-
potential adverse impact upon D.O. against the cost and ease ofcontrol. On both of these latter
points, adverse impact and cost, the balance weighs heavily towards the requested adjusted
standard relief. The beneficial impact, if any, to the Illinois River would be minimal if Noveon
were required to meet the ammonia nitrogen limitation of35 Ill. Adm. 304.122(b). Further,
given the lack of any discernible environmental benefit, the high cost ofthe technically feasible
control technology makes it economically unreasonable for Noveon to meet the ammonia
effluent limitation and warrants the requested adjusted standard relief.
3.
Environmental or Health Impacts
--
Section 28.1(c)(3)
There is no measurable impact upon the environment or human health that would result
from the granting of this adjusted standard. As discussed thoroughly in Section VII. in this
29
-
petition, the discharge from the Henry Plant will meet the winter and summer acute water quality
standards for ammonia at the edge of an appropriately calculated ZID. The winter and summer
acute and chronic standards will also be met at the edge of an appropriately calculated mixing
zone.
Thus, the impact will not be significantly more adverse than that contemplated by the
regulation ofgeneral applicability.
4.
Consistency With Federal Law
--
Section 28.1 (c)(4)
The requested adjusted standard is consistent with federal law. The requested relief
applies only to ammonia discharges from the Henry Plant. There are no applicable federal
numeric effluent standards or water quality standards for ammonia. Under federal regulations:
A water quality standard defines the water quality goals ofa water
body, or portion thereof, by designating the use or uses to be made
ofthe water and by setting criteria necessary to protect the uses~
States adopt water quality standards to protect public health or
welfare, enhance the quality ofwater and serve the purposes ofthe
Clean Water Act (the Act). “Serve the purposes ofthe Act” (as
defined in sections 101(a)(2) and 303(c) ofthe Act) means that
water quality standards should, wherever attainable, provide water
quality for the protection and propagation offish, shellfish and
wildlife and for recreation in and on the water and take into
consideration their use and value ofpublic water supplies,
propagation offish, shellfish, and wildlife, recreation in and on the
water, and agricultural, industrial, and other purposes including
navigation.
40 C.F.R. 131.2. Under 40 C.F.R. 13 1.4(a) “states are responsible for reviewing, establishing
and revising water quality standards.” In turn, pursuant to 40 C.F.R. 13
1.5(a),
“EPA is to review
and to approve or disapprove the State-adopted water quality standards.” These standards are to
be protective ofthe designated uses (~131.5(b))and, where those uses are not protected, this
must be supported by “appropriate technical and scientific data and analyses.”
(~
131
.5(b)(4)).
A
state is allowed to remove a designated use, which is not an existing use, if it “can demonstrate
30
BEFORE
THE
ILLINOIS POLLUTION CONTROL BOARD
iN THE MATTER OF:
)
)
Petition ofNoveon, Inc.
)
)
ASO2-____
)
(Adjusted Standard)
for an Adjusted Standard from
)
35111. Adm. Code 304.122
)
Exhibit List
1.
AquAeTer June 4, 2001 memorandum “Review ofDispersion Achievable
for Meeting Water Quality Limits at the PMD Group, Inc. Noveon
HenryFacility.”
2.
AquAeTer October 3, 2000 memorandum “Analysis ofDO in the Illinois
River Downstream from Henry, Illinois.”
3.
AquAeTer June 22, 2001 report “Mixing Zone/ZID Issues, Illinois River
at Henry, Illinois.”
4.
Wastewater Treatment Plant Block Flow Diagram.
5.
2001 Discharge Data Summary.
6.
Eckenfelder Inc. June 1996 “Evaluation ofTreatment Alternatives for
Reducing Final Effluent Ammonia Load.”
7.
Brown and Caidwell May 17, 2002 memorandum.
8.
Affidavit ofDavid E. Giffin.
1
-
opumizing environmental resources
• water, air, earth
~Ter
-
MEMORANDUM
TO:
Richard Kissel and Mark Latham, Gardner, Carton & Douglas
FROM:
Mike Corn,
P.E., AquAeTer
DATE:
June4, 2001
JOB NO:
001105
RE:
Review ofDispersion Achievable for Meeting Water Quality Limits at the PMD
Group, Inc., Henry Facility
In 1989, a dispersion study ofthe existing single port diffuser was conducted using specific
conductance at 25 °C(conductivity) as the tracer. From this information, dispersion from the
existing diffuser and physical dimensions ofthe zone ofinitial dilution (Z1D) and the total mixing
zone were estimated. Based on this tracer study, the diffuser was found to have a ZJD that extended
a total distance of
66.5
ft downstream, based on the discharge length scale, defined as the centerline
ofthe plume in the downstream direction, and the flux average dispersion (FAD) at the end of the
ZID. This distance was based on the in situ measurements of conductivity and also on the minimum
distance prescribed bythe Illinois Environmental Protection Agency (IEPA) forZIDs, which in this
case is based on 50
*
the square root ofthe cross-sectional area. The dispersion achieved at the edge
ofthe ZID based on the tracer study results of 13.2:1.
Additionally, in 1994 and 1995, as assessment ofthe Illinois River background water quality
conditions at Marseilles, Illinois were as follows:
Parameter
Units
Summer
Winter
Total Ammonia
mg/L
0.297
0.8
NH3,
75th
percentile
mg/L
0.011
0.005
Temperature,
75th
percentile
°C
26.0
6.5
pH, calculated
75th
percentile
S.U.
7.77
7.63
Based on the above data, the critical period for meeting water quality numeric effluent limits
was during surmner periods. Meeting the numeric water quality limits during winter conditions were
not an issue with this discharge based on the ZID described above and under the specified winter
time conditions.
A multiport high-rate diffuser was also conceptually designed to maximize the dispersion
from the combined PM) Group and City ofHenry discharge. Based on a flow of 1.0 million gallons
Mr. Richard Kissel, Gardner, Carton & Douglas
001 105/2
October 3,
2000
-
Page 2
be low compared to the upstream stations that were taken in the early to mid-
afternoon. Typically, DO in systems influenced by algae reflect average DO
concentrations in the diurnal cycle around noon to about 1400. Therefore, the
period average DO concentrations may be more reflective of River DO
conditions. Regardless, the DO concentrations are not reflective of a stressed
system, although there have been instances (grab samples) ofDO concentrations
less than the
5
milligrams per liter (mg/L) standard.
3.
Nitrogen concentrations at these four stations are around 0.75 to 1.7 mg/L total
kjeldahl nitrogen (organic plus ammonia-nitrogen). These are not excessive
nitrogen levels. It is unclear from the data how much ofthe TKN is ammonia, but
it appears to be on the order of 0.05 to 0.3 mg/L for September.
4.
Nitrate concentrations are high in the River upstream from Henry (i.e., 3 to 4
mg/L at Marseilles) and this is reflective ofnitrification in the River upstream.
5.
Phosphorous is very high in the Illinois River with total phosphorous recorded in
September around 0.5 mg/L. Phosphorous would control this system, because it
is in- excess of what is required by the algae. Total phosphorous in the range of
0.05 to 0.15 mg/L is a typical range. The BF Goodrich wastewaters are
phosphorous limited and the facility adds phosphorous to aid in the biological
process. The River phosphorous is most likely controlled by nonpoint sources
(i.e., farming and most likely the City ofChicago effluent discharges).
6.
The nitrogen to phosphorous ratio for healthy algae populations ranges from 60:1
to 10:1. Phosphorous at 100 ug/L for free-flowing streams and
50
ug/L for lake-
like settings is considered adequate for preventing nuisance algae blooms. For the
-
Illinois River, the N:P ratio is around .3:1, which would indicate that phosphorus
is in excess.
The U.S. Environmental Protection Agency (USEPA) wasteload allocation model,
QUAL2e, was utilized to project impacts of the BF Goodrich effluent to the Illinois River.
Model~inputs were projected from USGS and IEPA synoptic water quality data and from
deoxygenation and reaeration/algae productivity rates based on similar rivers where specific
wasteload allocation data have been collected. No specific assimilative capacity study data were
available from the agencies, although the Illinois Water Survey may have these data that may be
obtained through a Freedom ofInformation Act (FOJA) request.
The Henry discharge included both the BF Goodrich effluent and the Henry publicly
owned treatment works (POTW) discharge through the BF Goodrich effluent diffuser. The
- -~ -
ratio.,ultimateof 4:1.,carbonaecousThe followingbiochemicalinput parametersoxygen
demandwere (CBODU)used
for thewascombinedestimatedBFat
CBOD~/BODGoodrich
and5
Henry POTW discharge
-
October 3,2000
-
001105/3
Mr. Richard Kissel
Gardner, Carton & Douglas
-
Quaker Tower, Suite 3400
321 N. Clark Street
Chicago, Illinois 60610-4795
-
RE: Analysis of
DO
in the Illinois River Downstream from Henry, Illinois
Dear Mr. Kissel:
AquAeTer,
Inc. (AquAeTer)
has conducted screening level dissolved oxygen (DO)
modeling of the Illinois River from about Illinois River mile (IRM) 200 to IRM 170. The BF
Goodrich treated effluent diffuser discharges to the River at about IRM 198. Data obtained form
the United States Geological Survey (USGS) and the Illinois Environmental Protection Agency
(IEPA) were used to develop an input data set for the River which is presented in Attachment 1.
Stream hydraulic characteristics were estimated based on other similar river/lake settings at
similar river depths and widths. Specific points of interest from the available data are listed
below.
1.
The critical low-flow high-temperature month has been assumed to be September
-
-
when the 7-day 10-year low flow (7Q10) is around 2,900 cubic feet per second
(cfs) (at Marseilles) and the critical temperature is around 77.7 degrees Farenheit
•
(°F).
Location
Period Average
( of Saturation)
September Average
(
of Saturation)
Illinois R. c~Marseilles
109.9
101.8
Illinois R. ~
Flennepin
104.31
108.8
Illinois
R. ~ Lacon
97.60
96.4
Illinois R.
~
Peoria
106.52
.
94.2
Normally, 85 percent DO saturation is considered typical stream conditions.
These DO saturations are reflective of a stream- that is primarily reoxygenated by
the resident algae populations. It is important to note that the DO measurements
at the Water Intake at Peoria were taken around 10 am and would be expected to
optimizing environmental resources
+
water, air, earth
HI
ii’
a’
2.
DO saturation in the River ranges as follows:
P.O. Box 1187 +
Brentwoocl,-TN
+ 37024-1187 + Phone (615) 373.8532 + F’ax (615) 373-8512
2
Richard Kissel and Mark Latham, Gardner, Carton & Douglas
001105
June 4, 2001
-
Page 2
per day (mgd) from the PMD Group effluent discharge and 0.3 mgd from the
City
of Henry for a
total flow of 1.3 mgd, a 15 ft long diffuser with 4 4-in ports placed in 13 ft ofwater and with ports
at a 60 angle fro.m the bottom and parallel to the ambient current, a dispersion of 43:1 can be
achieved on the order ofone diffuser length downstream or from
7.5
to 22.5 ft downstream
(V2
to
1
V2
diffuser lengths). The dispersion modeling was completed for a 7-day 10-year low flow (7Q10)
that occurs in September. The CORMIX model was used to project the diffuser dispersion. The
diffuser would result in all numeric waterquality limits being met in the shortest distance from the
diffuser pipe and in the smallest area.
The information presented in this report has been developed using available LEPA, USEPA
or other governmental agencies and using published dispersion models and guidance on mixing
zones. Ifyou should have questions or comments concerning this information, please call me at
(615) 373-8532 or by FAX at (615) 373-8512 or by e-mail at mcorn~aquaeter.com.
MIXING ZONE/ZID ISSUES
ILLINOIS RIVER AT HENRY, ILLINOIS
NOVEON, INC.
HENRY, ILLINOIS
BF GOODRICH
BRECKSVILLE, OHIO
~er
215
JAMESTOWN PARK, SUITE
100
•
7340
EAST
CALEY AVE., SUITE 200
BRENTWOOD, TN 37027
CENTENNIAL, CO 80111
(615)
373-8532
(303) 771-9150
JUNE
22, 2001
optimizing environmentalresources~
water,
air, earth
3
Mr. Richard Kissel, Gardner, Carton & Douglas
001105/2
October 3, 2000
-
Page 4
Ifyou should have questions or comments concerning these analyses, please contact us at
(615)
373-8532, or by FAX at (615-373-8512, or by email at mcorn~aguaeter.com or
smccormick~aguaeter.com.
Sincerely,
AquAeTer, Inc.
~1mQC&ryuLdJ
____________
Shaleen T. McCormick
Michael R. Corn
j
Project Scientist
President
cc:
Mark Latham, Gardner, Carton & Douglas
Dave Giffin, BF Goodrich, Henry, Illinois
• Ken Willings, BF Goodrich, Cleveland, Ohio
1..•
Mr. Richard Kissel, Gardner, Carton & Douglas
00 1105/2
October 3, 2000
Page 3
SOURCE
FLOW
(mgd)
(mgIL)BOD5
CBODU
(mgfL)
ORG N
(mg/L)
NH3+NH4-N
(rng/L)
BFG
0.8
40
160
46
137
BFG
0.8
20
80
46
137
BFG
0.8
20
80
3
3
I-IenryPOTW
0.4
30
45
12
8
The values used for the BF Goodrich effluent have been input into the model using
maximumconcentrationconcentrationsof
40 mg/L isora
upperdaily
maximumranges
ofpermitconcentrations.limit
and theFordailyexample,average valuethe
BODis
205
mg/L. Monthly averages are used for projecting wasteload allocations. The CBOD~/BOD5ratio
of 4:1 for the Henry plant is estimated from past time-series BOD’s conducted on organic
chemical plants, which indicate this ratio is much higher than that traditionally estimated for
domestic effluents (1.5 to 2:1).
Model results for dissolved oxygen are presented in Figures 1 and 2. Model inputs and
outputs are presented in Attachment 2. The results include four model runs:
1.
The BOD5 in the BFG/Henry effluent discharge was set at 40 mg/L (daily
maximum);
2.
The BOD5 in the BFG/Henry effluent discharge was set at 20 mg/L (monthly
average
—
this is the allocation scenario that the allocation would be based on in
the discharge);
3.
The organic and ammonia nitrogen load from BFG was set at 6 mg/L; and
4.
The BFG/Henry effluent discharge was removed from the River.
Based on the input parameters used, the model indicated that the BFGIHenry discharge
reduced the DO in the River for the critical September 7Q10 condition from a DO sag low point
of7.74 mg/L without the BFG/Henry discharge to 7.58 mg/L with the BFG/Henry discharge or
an impact of about 0.16 mg/L. The impact appears to occur between about IRM 178.75 to about
174.5, which is at the head of the Peoria pool. Without the BFG/Henry discharge, this sag
occurs from about IRM 179 to about IRM
175.25,
or approximately in the same general area.
There is still a DO sag in the area downstream from Henry even without the Henry plant. This
appears to be reflected in the DO saturations recorded at Lacon, although firm conclusions
should not be drawn from grab samples.
The nitrogen load from BFG does not appear to be impacting algal productivity (i.e., not
impacting nutrient enrichment), but it does impact the DO resources in the River. Since the BFG
effluent
has a minimal impact, less than 0.2 mg/L or within the accuracy of our ability to
I
Illinois
.
measureRiver.DO
(+/..
0.1 mg~),the nitrogen load from BFG is not having an adverse effect on the
r~-
ACUTE
CHRONIC
TOXICITY
TOXICITY
CRITERIA
CRITERIA
ANTIBACKSLIDING
PROVISION
WHOLE EFFLUENT
WATER QUALITY
BASED LIMITS
ACUTE
CHRONIC
RIO-
TOXICITY
TOXICITY
ACCUMULATION
TESTING
TESTING
TESTING
ZID
1TTYT~
END OF PIPE
CLEAN WATER ACT OF 1987
WATER-QUALITY BASED TOXICS CONTROL
POLLUTANT BY
POLLUTANT
WATER QUALITY
BASED LIMITS
TECHNOLOGY
BASED
LIMITS
BAT
‘~
AND
• EFFLUENT LIMITS
GUIDELINES
V
NUMERIC OR
NARRATIVE
STANDARDS
CONVENTIONAL
AND
PRIORITY POLLUTANTS
V
HUMAN
f~ERRESTRIAL
HEALTH
LIFECYCLES
CRITERIA
CRITERIA
ANTIBACKSLIDING
PROVISION
END OF PIPE
y
.1
V
MIXING ZONE
TOTAL
END OF PIPE
TABLE 1.
EFFLUENT
AND
RIVER DATA
GENERAL CONDITIONS
Effluent Characteristics
Single-port submerged discharge pipe located
25 ft offshore at IRM 198.0
Average Effluent Flow
=
1.43 cfs or 0.92 mgd
Average Effluent TDS-~-6,500 mg/L (typical)
Average Effluent Conductivity
=
9,000-10,000 umhos/cm
River Characteristics
7Q10
=
3,400 cfs
Average
=
16,500 cfs
Conductivity
=
740 umhos/cm
OCTOBER 25, 1989 DISPERSION STUDY
Effluent
Q =
1.7
cfs cr1.1 mgd
TDS
=
7,000 mg/L
Conductivity
=
10,000 to 12,000 umhos/cm
River
o
=
6,550 cfs
Conductivity
=
775 umhos/cm
Plume
ZID
=
5:1 to 9:1
400 to 800 ft achieved complete vertical mixing
800 ft --.100:1
0
—
280
260
240
220
200
180
Li~I
160
0
IL-
Lii
120
0
z
~cioo
(I)
80
60
40
20
0
2$
—100 —50
0
50
100 150
200
50
300 350 4-00
450 500 550 600
650
700 750
800
DISTANCE
DOWNSTREAM FROM OUTFALL (ft)
FIGURE 2
LATERAL AND
LONGITUDINAL ISOPLETHS
FOR
BOTTOM
SPECIFIC CONDUCTANCE
r~
IWNOIS RIVER
CONDUCTNITY
—
775 umhoa/cm
EFFLUENT
CONDUCTIVI1Y
=
12.000
urnhos/crn
.
-~
—---.:~—
~
TABLE 2. DISPERSION
ACHIEVED FOR THE
EXISTING SINGLE-PORT
DIFFUSER
3,000
2,000
19.8
10.9
-
5.0
9.2
CONDUCTIVITY
ISOPLETH
-
(umhos/cm)
-
Back to top
EFFLUENT
()
Back to top
DISPERSION
Back to top
RATIO
L:1)
9,000
73.3
1.4
Back to top
900
liii
89.8
880
094
106.9
1,000
2.0
49.9
Table 3. Calculation ofAllowable Total Ammonia in ZID
USEPA Equation (“1999 Update ofAmbient Water Quality Criteria for Ammonia”,
USEPA, Office ofWater, September 1999):
CMC=
0.411
+
58,4
(1)
1
+
107.204
-
1
+
1
0pH
— 7.204
where:
CMC
=
criterion maximum concentration (acute criterion)
pH
=pHatedgeofZlD
Calculatingwhere:for CMC for Total ammonia or NH3
+
NIH4
pH 7.77 standard units (S.U.)
CMC
=
0.411
+
58A
1
+
107.204_7.77
1
+
1
~
—
7.204
CMC
=
(0.411/1.272)
+
(58.4/4.68
1)
=
0.323
+
12.475
CMC
=
12.8
rng/L
‘lotal Ammonia~
Note: The 1998 arid 1999 CMC equations for streams absent salmonids are equivalent.
—r r r c r~c
~t c r r
r r- -~r- —.
FIGURE 1
TOTAL AMMONIA
vs
ZID DISTANCE DOWNSTREAM
SUMMER
and
WINTER
ZID DISTANCE (It)
SUMMER
WINTER
-I-
—•-
600
500
I
~200
100
0
0
20
40
60
80
100
120
CALCULATION OF ALLOWABLE EFFLUENT AMMONIA
CONCENTRATIONS FOR THE SINGLE PORT DIFFUSER
(BF GOODRICH PROPOSED ZID)
The BF Goodrich effluent characteristics are assumed to be as follows:
Effluent
Q
0.8 mgd or
556
gpm
Effluent TDS
10,361 mgIL
Effluent NH3+ NH4
Variable depending upon dispersion
BFG Effluent pH
7.00 S.U.
ZID pH
7.77 S.U.
Background River NH3÷NH4
0.297 mg/L (summer conditions)
ZID NH3÷NH4 CMC
12.80 mgfL (see Table 1)
ZID TDS WET Conc.
•
1,500 mg/L (to meet WET)
The effluent concentration can be calculated from the ZID required CMC or WET value as
follows.
Assume:
S
=
13.2
S
=
13.2
=
12.2 parts background river water and 1 part effluent
Therefore:
(13.2 total parts at edge of ZID
*
12.80 mgfL NH3+ NH4 CMC)
=
(1 part effluent
*
x mgfL NH3÷NH4
) +
(12.2 parts river
*
0.297 mgIL NH3+ NH4)
x
=
(168.96 mg/L
*
parts —3.62 mgIL
*
parts)/(1 part)
x
=
165.3 mg/L effluent Total NH1+ NH4 allowable for S
=
13.2:1
~er
CONSIDERATION OF
BF GOODRICH
AND
CITY OF HENRY POTW COMBINED
EFFLUENT
1,516.5
lbs/day
=
(0.3
mgd
*
20 mgfL
*
8.34)
+ (0.8 mgd *
x
*
8.34)
x
=
(1,516.5
lbs/day
—
50.04
lbs/day)/6.67 (mgd
*
lbs/day)/(mgfL
*
mgd)
x
= 219.8
mg/L total ammonia that can be discharged from BF Goodrich
MINIMUM
DISPERSION
REQUIRED
TO MEET ACUTE TOXICITY
DUE TO TOTAL DISSOLVED SOLIDS (TDS)
(x
+
1)(1,500mgIL TDS)
= (x)(481
mgfL
TDS) + (1)(10,361
mg/L TDS)
1,500 mgIL x
+
1,500 mgfL
=
481 mg/L x
+
10,361 mg/L
1,500 mg/L x
-
481 mgfL x
=
10,361 mgfL
1,Ol9mg/Lx
=
8,861 mg/L
x
=
8,861 mgfLil,019 mgfL
=
8.7:1
to meet 1,500 mg/L TDS at edge of ZID
With Henry POTW x
=
8.2:1
to meet 1,500 mgfL TDS at edge ofZID
1111111
Mr. Richard J. Kissel
-
0
4
October
9,
1998
1••~~
~.•
-
-
-
I
-
Diffusion Requirements
ARCHITECTSENGINEERS
AquAeTer’sThe
above assumptionsMike
Corn. AquAelerand
conceptual
recommends
plan and
use
profileof
the
layouts
following
were
design
discussed
parameters
with
as
PLANNERS
it relates to the diffusion header. As recommended by AquAeTer, the port size, length of
diffusion header, angle of ports and port spacing as shown below, will provide a
dispersion of about 43:1 at one diffuser length downstream at 7Q10 flow (low pool)
conditions.
Length of Diffusion Header~
15 ft.
Design Flow Rate:
1.3 MGD
Port Velocity at Avg. Design Flow Rate:
10 FPS
-
No.
of Ports:
9
Port Diameter~
2 inches
Port Angle (from horizontal):
60 degrees
Centerline Distance Between Ports:
1.67 ft.
Dispersion:
43:1
-
Other Hydraulic Determinations
As previously discussed, flows above the average design flow would cause higher
velocities and associated greater head loss through the diffusion system. The following
outlines various port exit velocities and the corresponding total hydraulic headloss through
the diffusion system at various flows.
Flow (MGD)
Port Exit Velocity (FPS)
Hydraulic Headloss (Feet)
1.3
9.9
-
2.9
1.6
12.1
4.4
2.1
15.9
7.6
2.4
18.2
9.9
4.7
-
35.6
37.8
5.0
37.9
42.7
95U~KI~eI.O98
~~IUT
0
B.F. Goodrich
-
Henry,
Illinois Facility
Multlport DiffusIon
System
Estimate of
Probable
Construction Costs
NGINEERS
~CHITECTS
Lt~m
Cost
- PLANNERS
Land mobilization
$15,000
River Mobilization
-
13,000
Bonds and Insurance
0
8,000
Excavation for Manholes
15,000
Excavation for Piping
0
45,000
Backfill
15,000
Rip Rap
20,000
Concrete Cast-in-Place Outfall Manhole
40,000
Handrail, Ladders and Fall Prevention System
.
15,000
Sheet Pile for Outfall Manhole
30,000
Foundation Piling for Outfall Manhole
3,000
Dewatering
10,000
Set-Over Precast Concrete Manhole
8,000
Closure Gates
-
30,000
Connection to Existing Manhole
3,000
Connection to Existing Pipe Line
2,000
Interconnecting pipe, Fittings and Appurtenances
12,000
Outfall Pipe Line
-
0
125,000
Diffusion Header and Ports
20,000
Pile Bent Placement and Support System
140,000
Miscellaneous
-
10,000
Subtotal
$579,000
Contingencies (15)
0
87.000
Total Construction Cost
$666,000
4
P:/PROJ/21522IFig 1
FIGURE 1
BLOCK FLOW DIAGRAM OF WASTESTREAM
SOURCES AND WWTF
Nashville, Tennessee
BROWN
AND
CALD WELL
01
-
-
---~-~--
—---—-----
----—~-
----I-——-
DMR Support Data
-
2001
Plant Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mgIL)
(parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Jan
12
8
539.09
77.63
51.75
7.5
70
2-Jan
12
7
434.98
62.64
36.54
7.5
68
3-Jan
12
49
211.00
30.38
124.07
7.6
64
4-Jan
6
11
561.24
40.41
74.08
6.3
77
5-Jan
609.07
7.3
80
6-Jan
738.33
7
78
7-Jan
6
10
653.49
47.05
78.42
7.5
78
8-Jan
10
9
685.71
82.29
74.06
7.6
66
9-Jan
38
9
524.84
239.33
56.68
7.5
72
10-Jan
-
8
8
492.62
47.29
47.29
7.5
70
11-Jan
4
6
511.02
24.53
36.79
7.5
73
12-Jan
472.49
7.5
72
13-Jan
648.18
7.9
73
14-Jan
4
6
632.08
30.34
45.51
7.3
72
15-Jan
10
10
110
0.054
0.09
6
3
501.83
36.13
18.07
7
66
16-Jan
5
4
401.13
24.07
19.25
7.2
73
17-Jan
5
4
503.21
30.19
24.15
7
63
18-Jan
3
3
549.00
19.76
19.76
7.3
66
19-Jan
457.22
7.8
70
20-Jan
278.02
7.7
70
21-Jan
11
7
462.33
61.03
38.84
7.8
70
22-Jan
4
2
587.03
28.18
14.09
6.5
74
23-Jan
5
3
533.10
31.99
19.19
6.2
78
24-Jan
8
6
512.90
49.24
36.93
6.7
78
25-Jan
6
5
499.33
35.95
29.96
6.5
78
26-Jan
502.47
6.6
70
27-Jan
544.23
6.7
73
28-Jan
4
4
547.12
26.26
26.26
6.7
64
29-Jan
6
6
604.60
43.53
43.53
6.7
73
30-Jan
5
8
697.49
41.85
66.96
6.8
70
31-Jan
J
6.4
624.62
52.47
47.97
6.9
73
Average
10.000
10.000
110.000
0.054
0.090
8.130
8.017
532.896
50.545
44.790
7.148
71.677
Maximum
10.000
10.000
110.000
0.054
0.090
38.000
49.000
738.330
239.327
124.068
7.900
80.000
Minimum
10.000
10.000
110.000
0.054
0.090
3.000
2.000
211.000
19.764
14.089
6.200
63.000
Ww12001 Jan
-
5/22/02 11:23 AM
DMR Support Data - 2001
Plant Effluent
Vinyl
Focal
Residual
tBOD
TSS
Date
Chloride Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#11
00 mL) (mg/L)
(mg/L) (parts/MM) (mg/I)
(mg/I)
(gpm)
(#Iday)
(#Iday)
(F)
1-Feb
-
4
16
503.81
24.18
96.73
6.9
70
2-Feb
367.63
6.9
66
3-Feb
363.40
6.9
70
4-Feb
4
2.4
491.11
23.57
14.14
6.9
75
5-Feb
4
3.2
587.66
28.21
22.57
7.3
73
6-Feb
6
5.2
300.00
21.60
18.72
7.3
66
7-Feb
5
7.6
494.97
29.70
45.14
7.4
70
8-Feb
0
5
13
730.47
43.83
113.95
7.3
73
9-Feb
-
608.08
7.4
78
10-Feb
702.58
6.7
80
11-Feb
7
6.4
455.51
38.26
34.98
6.8
72
12-Feb
10
5.6
504.81
60.58
33.92
7
68
13-Feb
21
8
642.72
161.97
61.70
6.9
72
14-Feb
15
21
636.33
114.54
160.36
6.9
75
15-Feb
32
24
639.73
245.66
184.24
7
73
16-Feb
501.79
7.6
75
17-Feb
498.53
7.4
57
18-Feb
22
30
495.49
130.81
178.38
7.3
68
19-Feb
28
21
664.23
223.18
167.39
7.3
73
20-Feb
24
25
651.30
187.57
195.39
7.5
73
21-Feb
10
0
140
0.068
0.344
15
16
608.38
109.51
116.81
7.6
66
22-Feb
21
49
553.56
139.50
325.49
7.2
70
23-Feb
629.09
8.3
64
24-Feb
634.60
7.4
68
25-Feb
32
14
653.04
250.77
109.71
7.1
70
26-Feb
14
10
501.26
84.21
60.15
7.3
79
27-Feb
16
8.4
554.22
106.41
55.87
7
78
28-Feb
13
5.2
518.41
80.87
32.35
7
78
Average
10.000
0.000
140.000
0.068
0.344
14.900
14.550
553.311
105.246
101.400
7.200
71.429
Maximum
10.000
0.000
140.000
0.068
0.344
32.000
49.000
730.470
250.767
325.493
8.300
80.000
Minimum
10.000
0.000
140.000
0.068
0.344
4.000
2.400
300.000
21.600
14.144
6.700
57.000
-
Ww12001 F~b
5/22/02 11:23AM
DMR Support Data - 2001
Plant Effluent
-
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mg/L)
(parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Mar
6.1
5.2
493.66
36.14
30.80
6.8
79
2-Mar
569.01
6.9
68
3-Mar
600.80
7
72
4-Mar
13
7.6
581.66
90.74
53.05
7.3
64
5-Mar
8
5.6
415.74
39.91
27.94
7
70
6-Mar
10
5.6
463.61
55.63
31.15
6.8
68
7-Mar
0
7.6
418.28
35.14
38.15
6.8
8-Mar
14
8
506.11
- 85.03
48.59
6.7
68
9-Mar
514.14
6.7
70
10-Mar
.
433.90
6.3
72
11-Mar
11
11
487.18
64.31
64.31
6.4
73
12-Mar
-
6
9.6
633.74
45.63
73.01
6.9
78
13-Mar
10
0
120
0.11
17
16
665.01
135.66
127.68
7
72
14-Mar
0.196
15
6
670.57
120.70
48.28
7.2
72
15-Mar
9
6.4
619.60
66.92
47.59
7
16-Mar
637.14
7
68
17-Mar
626.87
7.2
66
18-Mar
7
4.8
647.50
54.39
37.30
7.1
70
19-Mar
11
4.4
595.87
78.65
31.46
7.1
72
20-Mar
9
7.2
563.66
60.88
48.70
7.2
70
21-Mar
9
7.6
528.79
57.11
48.23
7
70
22-Mar
11
8.4
519.49
68.57
52.36
7.1
71
23-Mar
507.06
7.2
70
24-Mar
488.70
7
70
25-Mar
5
8
487.76
29.27
46.82
7.1
66
26-Mar
7
2.8
392.56
32.98
13.19
7
71
27-Mar
8
5.2
431.69
41.44
26.94
7.3
71
28-Mar
-.
16
8
379.69
72.90
36.45
7.2
71
29-Mar
16
3.6
430.44
82.64
18.60
7.6
72
30-Mar
425.12
6.8
73
31-Mar
445.81
7.7
74
Average
10.000
0.000
120.000
0.110
0.196
10.243
7.076
521.973
64.506
45.266
7.013
71.000
Maximum
10.000
0.000
120.000
0.110
0.196
17.000
16.000
670.570
135.662
127.682
7.700
79.000
Minimum
10.000
0.000
120.000
0.110
0.196
5.000
2.800
379.690
29.266
13.190
6.300
64.000
Wwt200l Mar
5/22/02 11:07 AM
DMR Support Data - 2001
Plant Effluent
I-Apr
2-Apr
3-Apr
4-Apr
5-Apr
6-Apr
7-Apr
8-Apr
9-Apr
10-Apr
11-Apr
12-Apr
13-Apr
14-Apr
15-Apr
16-Apr
17-Apr
18-Apr
19-Apr
20-Apr
21-Apr
22-Apr
23-Apr
24-Apr
25-Apr
26-Apr
27-Apr
28-Apr
29-Apr
30-Apr
Vinyl
Fecal
Residual
Chloride Coliform Ammonia
Phenol
Chlorine
tBOD
(ug/L)
(#11
00 mL)
(mg/L)
(mg/L) (parts/MM)
(mg/I)
tBOD
TSS
TSS
Flow
Load
Load
pH
Temp.
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
9
5.6
577.47
25
18
510.17
21
20
447.16
12
19
541.42
15
24
540.00
575.02
657.02
14
21
625.63
11
6.4
610.51
20
15
600.82
15
26
629.01
15
10
297.29
524.93
606.28
7
4
621.76
10
5.2
500.54
11
16
511.07
15
21
512.59
11
10
626.82
516.97
539.63
10
12
545.40
12
10
623.27
13
.19
554.26
10
18
499.50
12
- 12
466.23
359.08
323.91
12
10
365.23
12
14
417.91
62.37
38.81
153.05
110.20
112.68
107.32
77.96
123.44
97.20
155.52
105.11
157.66
80.59
46.89
144.20
108.15
113.22
196.25
53.51
35.67
52.23
29.84
60.06
31.23
67.46
98.13
92.27
129.17
82.74
75.22
65.45
78.54
89.75
74.79
86.46
126.37
59.94
107.89
67.14
67.14
52.59
43.83
60.18
70.21
Ww12001 Apr
5/22/02 11:07 AM
Date
0.213
10
10.000
10.000
10.000
7.5
7.5
7.4
7.2
7.2
7.2
7.2
7.4
7.4 -
7.3
7.3
7.3
7.3
7
7.4
7.3
7.2
7.2
7.2
7.4
7.7
7.3
7.3
7.2
7.2
7.1
0
130
0.08
0.000
130.000
0.080
0.000
130.000
0.080
0.000
130.000
0.080
72
70
72
74
73
75
75
75
72
77
75
75
71
72
71
73
72
74
75
73
74
73
75
73
72
72
Average
Maximum
Minimum
7.4
73
0.213
13.273
0.213
25.000
0.213
7.000
14.373
524. 230
26.000
657.020
4.000
297.290
7.3
7.2
7.2
7.293
7.700
7.000
73
72
75
73.267
77.000
70.000
83.462
91 .467
153.051
196.251
52.228
29.844
DMR Support Data
-
2001
Plant Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mg/L) (parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Jun
440.50
7.1
70
2-Jun
609.21
7.1
70
3-Jun
6
6
544.06
39.17
39.17
7.2
70
4-Jun
6
13
424.52
30.57
66.23
7.3
72
5-Jun
.
4
27
477.14
22.90
154.59
7.3
70
6-Jun
4
10
507.63
24.37
60.92
7.3
75
7-Jun
5
6
540.92
32.46
38.95
7.3
76
8-Jun
476.53
7.3
77
9-Jun
436.44
7.3
77
10-Jun
5
7
462.43
27.75
38.84
7.4
77
11-Jun
10
10
100
0.11
0.187
6
19
475.06
34.20
108.31
7.2
75
12-Jun
7
7
563.24
47.31
47.31
7.2
74
13-Jun
8
6NoData
7.1
75
14-Jun
9
9
569.84
61.54
61.54
7.1
76
15-Jun
616.74
7.3
81
16-Jun
580.42
7.2
79
17-Jun
19
36
484.49
110.46
209.30
7
81
18-Jun
5
16
490.60
29.44
94.20
7.3
82
19-Jun
11
28
565.22
74.61
189.91
7.1
82
20-Jun
11
32
647.21
85.43
248.53
7.1
82
21-Jun
11
42
602.44
79.52
303.63
7.5
78
22-Jun
533.94
7
78
23-Jun
-
634.64
6.9
77
24-Jun
3
17
617.77
22.24
126.03
7
80
25-Jun
6
15
664.29
47.83
119.57
7.3
82
26-Jun
25
33
597.46
179.24
236.59
7.1
80
27-Jun
13
27
568.40
88.67
184.16
7.1
78
28-Jun
12
20
649.22
93.49
155.81
7.1
82
29-Jun
631.81
7.2
80
30-Jun
630.63
7.1
81
Average
10.000
10.000
100.000
0.110
0.187
8.800
18.800
553.200
59.537
130.716
7.183
77.233
Maximum
10.000
10.000
100.000
0.110
0.187
25.000
42.000
664.290
179.238
303.630
7.500
82.000
Minimum
10.000
10.000
100.000
0.110
0.187
3.000
6.000
424.520
22.240
38.844
6.900
70.000
Ww!2001
June
5/22/02 11:07 AM
DMR Support Data
-
2001
Plant Effluent
Vinyl
Focal
Residual
Chloride Coliform Ammonia
Phenol
Chlorine
tBOD
(ug/L)
(#/100 mL)
(mg/L)
(mg/L) (parts/MM)
(mg/I)
tBOD
TSS
TSS
Flow
Load
Load
pH
Temp.
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Jul
2-Jul
3-Jul
4-Jul
5-Jul
6-Jul
7-Jul
8-Jul
9-Jul
10-Jul
11-Jul
12-Jul
13-Jul
14-Jul
15-Jul
16-Jul
17-Jul
18-Jul
19-Jul
20-Jul
21-Jul
22-Jul
23-Jul
24-Jul
25-Jul
26-Jul
27-Jul
28-Jul
29-Jul
30-Jul
31-Jul
19
584.87
14
460.51
3
669.34
3
616.73
2
536.26
602.67
637.07
3
3
625.00
4
5
546.52
6
9
718.98
9
15
775.62
9
27
728.89
666.09
633.08
3
11
583.43
5
6
586.56
9
15
589.83
6
13
674.00
7
18
679.06
721.81
692.31
6
18
670.24
9
18
678.44
6
21
748.13
10
30
701.43
4
17
711.94
669.36
671.39
3
6
639.49
4
549.88
5
643.63
12.261
645.566
30.000
775.620
2.000
460.510
21.06
133.35
44.21
77.37
32.13
24.10
37.00
22.20
19.31
12.87
22.50
22.50
26.23
32.79
51.77
77.65
83.77
139.61
78.72
236.16
21.dO
77.01
35.19
42.23
63.70
106.17
48.53
105.14
57.04
146.68
48.26
144.77
73.27
146.54
53.87
188.53
84.17
252.51
34.17
145.24
23.02
46.04
26.39
26.39
30.89
38.62
44.183
97.586
84.172
252.515
19.305
12.870
7.7
82
7.5
80
7.3
82
7.4
83
7.3
83
7.206
81 .323
7.700
88.000
6.400
77.000
Ww12001 July
5/22/02 11:07 AM
Date
3
8
4
5
3
7.1
7.2
7.3
6.8
7.1
6.4
6.9
6.9
6.8
6.8
7.3
7.2
7.4
7.4
6.9
7.3
7
7.4
7.1
7.2
7.4
7.3
7.4
7.5
7.6
7.5
82
77
80
83
80
81
79
82
81
80
77
81
82
81
82
80
80
82
80
82
88
83
85
82
81
80
10
80
96
0.088
0.363
4
4
10.000
80.000
96.000
0.088
0.363
5.652
10.000
8b.000
96.000
0.088
0.363
10.000
10.000
80.000
96.000
0.088
0.363
3.000
Average
Maximum
Minimum
DMR Support Data - 2001
Plant Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform
Ammonia
Phenol
Chlorine
IBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mg/L) (parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Aug
5
12
767.71
46.06
110.55
7.4
83
2-Aug
11
6
834.40
110.14
60.08
7.3
81
3-Aug
781.00
7.1
81
4-Aug
5
72
778.07
46.68
672.25
7.4
82
5-Aug
9
29
766.51
82.78
266.75
7.5
80
- 6-Aug
*
751.20
7.3
80
7-Aug
0
*
No Data
8-Aug
15
26
NoData
9-Aug
13
100
123.38
19.25
148.06
7.4
82
10-Aug
642.79
7.2 -
80
11-Aug
812.18
7.6
77
12-Aug
5
12
603.76
36.23
86.94
6.7
78
13-Aug
7
25 -
471.12
39.57
141.34
7.3
80
14-Aug
10
30
110
0.084
0.24
6
15
474.07
34.13
85.33
7.5
77
15-Aug
11
13
504.01
66.53
78.63
7.3
78
16-Aug
5
4
599.26
35.96
28.76
7.2
72
17-Aug
537.78
7.3
72
18-Aug
501.98
7.7
72
19-Aug
6
16
560.87
40.38
107.69
7.3
75
20-Aug
11
10
569.69
75.20
68.36
7.3
80
21-Aug
8
20
680.96
65.37
163.43
7.5
79
22-Aug
8
12
683.12
65.58
98.37
7.4
77
23-Aug
13
12
550.96
85.95
79.34
7.5
77
24-Aug
672.83
7.5
77
25-Aug
0
634.53
7.6
77
26-Aug
5
27
625.36
37.52 - 202.62
7.6
80
27-Aug
3
17
608.31
21.90
124.10
7.7
77
28-Aug
12
38
537.47
77.40
245.09
7.6
76
29-Aug
12
36
535.01
77.04
231.12
7.8
78
30-Aug
14
14
556.98
93.57
93.57
7.8
80
31-Aug
420.29
7.6
85
Average
10.000
30.000
110.000
0.084
0.240
8.762
24.571
606.400
57.862
154.618
7.428
78.379
Maximum
10.000
30.000
110.000
0.084
0.240
15.000
100.000
834.400
110.141
672.252
7.800
85.000
Minimum
10.000
30.000
110.000
0.084
0.240
3.000
4.000
123.380
19.247
28.764
6.700
72.000
* NoDataduetoPlantShutdown
5/22/02
Wwt200l
11:07
Aug
AM
DMR Support Data
-
2001
Plant Effluent
Vinyl
Fecal
Residual
1BOD
TSS
Date
Chloride Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mg/L) (parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#Iday)
(F)
1-Sep
594.99
7.6
84
2-Sep
7
20
533.58
44.82
128.06
7.4
86
3-Sep
-
6
20
548.92
39.52
131.74
7.5
88
4-Sep
8
10
516.52
49.59
61.98
7.5
88
5-Sep
12
10
559.53
80.57
67.14
7.5
86
6-Sep
10
31
578.06
69.37
215.04
7.5
86
7-Sep
658.01
7.5
80
8-Sep
725.20
7.5
80
9-Sep
6
14
698.70
50.31
117.38
7.5
80
10-Sep
6
9
578.60
41.66
62.49
7.3
86
11-Sep
8
8
570.18
54.74
54.74
7.3
85
12-Sep
11
12
583.73
77.05
84.06
7.3
77
13-Sep
4
23
552.36
26.51
152.45
7.4
79
14-Sep
472.39
7.4
82
15-Sep
458.39
7.4
78
16-Sep
15
36
594.80
107.06
256.95
7.2
76
17-Sep
10
10
150
0.1
0.7
14
33
547.29
91.94
216.73
7.4
83
18-Sep
15
22
537.03
96.67
141.78
7.4
84
19-Sep
16
37
556.23
106.80
246.97
7.3
83
20-Sep
13
31
531.63
82.93
197.77
7.5
77
21-Sep
-
618.67
7.4
78
22-Sep
765.58
7.4
76
23-Sep
7
44
668.17
56.13
352.79
7.6
84
24-Sep
0
12
44
562.74
81.03
297.13
7.4
74
25-Sep
-
-
13
42
479.71
74.83
241.77
7.9
80
26-Sep
8
22
478.18
45.91
126.24
7.2
76
27-Sep
9
13
554.79
59.92
86.55
7.5
78
28-Sep
582.08
7.4
70
29-Sep
433.97
-
7.1
70
30-Sep
22
30
481.14
127.02
173.21
7.3
70
Average
#DIV/0!
10.000
150.000
0.100
0.700
10.571
24.333
567.372
69.732
162.522
7.420
80.133
Maximum
0.000
10.000
150.000
0.100
0.700
22.000
44.000
765.580
127.021
352.794
7.900
88.000
Minimum
0.000
10.000
150.000
0.100
0.700
4.000
8.000
433.970
26.513
54.737
7.100
70.000
Ww12001 Sep
5/22/02 11:07 AM
DMR Support Data
-
2001
Plant Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mgIL) (parts/MM)
(mg/I)
(mg/I)
(gpm)
(#Iday)
(#/day)
(F)
1-Oct
16
15
537.71
103.24
96.79
7.2
80
2-Oct
11
38
536.67
70.84
244.72
7.0
78
3-Oct
13
16
573.01
89.39
110.02
7.0
82
4-Oct
10
42
540.48
64.86
272.40
7.0
80
5-Oct
632.27
7.6
78
6-Oct
674.20
7.6
76
7-Oct
19
34
690.77
157.50
281.83
7.3
77
8-Oct
9
26
553.06
59.73
172.55
7.5
76
9-Oct
12
12
495.79
71.39
71.39
7.2
77
10-Oct
- 13
14
547.23
85.37
91.93
7.1
84
11-Oct
12
21
684.88
98.62
172.59
7.1
79
12-Oct
675.28
6.9
78
13-Oct
693.32
7.0
76
14-Oct
23
23
623.73
172.15
172.15
7.1
72
15-Oct
40
46
489.76
235.08
270.35
6.8
75
16-Oct
10
0
100
0.079
0.461
23
18
648.44
178.97
140.06
6.8
70
17-Oct
13
15
596.18
93.00
107.31
6.9
70
18-Oct
10
11
493.31
59.20
65.12
6.6
74
19-Oct
429.39
6.7
76
20-Oct
535.18
6.7
77
21-Oct
9
4
568.39
61.39
27.28
6.9
73
22-Oct
11
6
559.59
73.87
40.29
7.0
75
23-Oct
12
21
432.28
62.25
108.93
7.1
70
24-Oct
10
19
402.41
48.29
91.75
7.0
79
25-Oct
10
10
424.56
50.95
50.95
7.4
72
26-Oct
421.70
7.1
66
27-Oct
589.66
6.9
63
28-Oct
12
12
614.08
88.43
88.43
7.0
64
29-Oct
8
10
432.18
41.49
51.86
7.0
73
30-Oct
13
6.8
423.16
66.01
34.53
6.7
78
31-Oct
20
9
427.16
102.52
46.13
6.9
76
Average
10.000
0.000
100.000
0.079
0.461
14.304
18.643
546.640
92.806
122.147
7.035
74.968
Maximum
10.000
0.000
100.000
0.079
0.461
40.000
46.000
693.320
235.085
281.834
7.600
84.000
Minimum
10.000
0.000
100.000
0.079
0.461
8.000
4.000
402.410
41.489
27.283
6.600
63.000
Wwt200l Oct
5/22/02 11:07AM
DMR Support Data - 2001
Plant
Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/1 00 mL)
(mg/L)
(mg/L)
(parts/MM)
(mgil)
(mg/I)
(gpm)
(#/day)
(4t/day)
(F)
1-Nov
9
6
477.08
51.52
34.35
6.9
75
2-Nov
620.56
6.9
77
3-Nov
523.24
7.2
77
4-Nov
20
11
484.02
116.16
63.89
7
79
5-Nov
20
10
462.67
111.04
55.52
7.3
73
6-Nov
.
33
2
407.17
161.24
9.77
7.3
72
7-Nov
22
11
436.79
115.31
57.66
7.3
73
8-Nov
0
10
11
571.82
68.62
75.48
7.2
77
9-Nov
536.97
7.3
73
10-Nov
635.73
7.1
72
11-Nov
8
5
542.86
52.11
32.57
7.2
72
12-Nov
10
14
432.28
51.87
72.62
7.4
75
13-Nov
10
23
464.84
55.78
128.30
7.2
77
14-Nov
10
0
100
0.051
0.344
17
18
516.90
105.45
111.65
7.4
81
15-Nov
13
16
464.14
72.41
89.11
7.5
81
16-Nov
474.67
7.4
80
17-Nov
470.73
7.1
79
18-Nov
14
13
449.29
75.48
70.09
7.4
80
19-Nov
27
17
487.48
157.94
99.45
7.4
68
20-Nov
35
22
547.01
229.74
144.41
7.5
68
21-Nov
29
17
434.63
151.25
88.66
7.3
72
22-Nov
36
23
315.34
136.23
87.03
7
72
23-Nov
411.74
6.9
73
24-Nov
457.19
6.8
70
25-Nov
26
24
404.78
126.29
116.58
6.9
72
26-Nov
17
28
305.81
62.39
102.75
6.5
73
27-Nov
23
30
395.98
109.29
142.55
6.8
72
28Nov
44
47
48634
25679
27430
7
78
29-Nov
15
34
383.46
69.02
156.45
6.8
79
30-Nov
462.80
6.8
73
Average
10.000
0.000
100.000
0.051
0.344
20.857
18.190
468.811
111.236
95.867
7.127
74.767
Maximum
10.000
0.000
100.000
0.051
0.344
44.000
47.000
635.730
256.788
274.296
7.500
81.000
Minimum
10.000
0.000
100.000
0.051
0.344
8.000
2.000
305.810
51.525
9.772
6.500
68.000
1111111. Non-Compliance
Wwt200l Nov
5/22/02 11:07 AM
DMR Support Data - 2001
-
Plant Effluent
Vinyl
Fecal
Residual
tBOD
TSS
Date
Chloride
Coliform Ammonia
Phenol
Chlorine
tBOD
TSS
Flow
Load
Load
pH
Temp.
(ug/L)
(#/100 mL)
(mg/L)
(mg/L)
(parts/MM)
(mg/I)
(mg/I)
(gpm)
(#/day)
(#/day)
(F)
1-Dec
484.51
6.7
73
2-Dec
23
69
482.63
133.21
399.62
7.2
77
3-Dec
19
43
421.99
96.21
217.75
7.1
75
4-Dec
20
40
454.23
109.02
218.03
7.0
79
5-Dec
23
44
433.10
119.54
228.68
7.0
- 80
6-Dec
24
30
445.52
128.31
160.39
7.1
77
7-Dec
-
425.00
7.3
75
8-Dec
463.17
7.5
73
9-Dec
31
18
483.96
180.03
104.54
7.3
70
10-Dec
17
24
487.51
99.45
140.40
7.4
75
11-Dec
26
18
563.61
175.85
121.74
7.1
73
12-Dec
43
51
587.48
303.14
359.54
7.1
73
13-Dec
17
37
236.34
48.21
104.93
7.9
72.
14-Dec
563.48
7.8
73
15-Dec
-
687.21
7.2
72
16-Dec
10
0
120
0.062
29
24
565.32
196.73
162.81
7.0
73
17-Dec
16
32
506.44
97.24
194.47
7.3
75
18-Dec
0.537
15
16
536.98
96.66
103.10
7.1
72
19-Dec
12
7
597.00
85.97
50.15
7.0
70
20-Dec
-
10
11
636.27
76.35
83.99
6.9
66
21-Dec
600.88
7.1
72
22-Dec
379.59
6.6
70
23-Dec
14
16
421.04
70.73
80.84
6.8
68
24-Dec
16
21
420.54
80.74
105.98
7.0
66
25-Dec
16
27
216.78
41.62
70.24
6.6
64
26-Dec
15
48
329.40
59.29
189.73
6.5
63
27-Dec
14
22
294.05
49.40
77.63
6.8
64
28-Dec
410.46
6.8
68
29-Dec
.
.
480.82
6.6
61
30-Dec
-
15
23
119.16
21.45
32.89
6.2
55
31-Dec
0
11
25
210.13
27.74
63.04
6.5
58
Average
10.000
0.000
120.000
0.062
0.537
19.364
29.364
449.826
104.404
148.658
7.016
70.387
Maximum
10.000
0.000
120.000
0.062
0.537
43.000
69.000
687.210
303.140
399.618
7.900
80.000
Minimum
10.000
0.000
120.000
0.062
0.537
10.000
7.000
119.160
21.449
32.888
6.200
55.000
Wwt200l Dec
5/22/02 11:08 AM
6
DRAFT
EVALUATION OF TREATMENT
ALTERNATIVES
FOR REDUCING
FINAL
EFFLUENT
AMMONIA LOAD
Prepared for:
BF GOODRICH
Henry, Illinois
Prepared by:
ECKENFELDER INC.®
227 French Landing Drive
Nashville, Tennessee 37228
(615) 255-2288
February 1997
9387.01
Q:\9387.O1\TS\TSCVR.DOC
ECKENFELDER INC?
February 18, 1997
9387.01
Mr. Dave Giffin
Health, Safety and Environmental Manager
BF Goodrich
R.R. 1, Box 15
Henry, IL 61537
RE: Evaluation of Treatment Alternatives for
Reducing Final Effluent Ammonia Load
Dear Mr. Gi.ffln:
We are pleased to submit our Draft Report, “Evaluation of Treatment Alternatives
for Reducing Final Effluent Ammonia Load.” This Report presents the background,
methods and materials, and results of our work. We will
prepare a
Final Report
that addresses your review comments.
If you have any questions or need additional information, please contact me.
Sincerely,
ECKENFELDER INC.®
~.
~th
~t774.1
T. Houston Flippin, P.E.
0
Project Manager
cc: Richard K.issel, Esquire
-
Gardner, Carton & Douglas
Ken Willings
-
BF Goodrich
W. Wesley Eckenfeld.er,
Jr.,
D.Sc., P.E.
227 French Landing
Drive
Nashville, Tennessee 37228
Q:\9387.O1\TS\TSL0218.DOC
615.255.2288
FAX
615.256.8332
TABLE OF CONTENTS
PaEe No.
Letter of Transmittal
Table of Contents
j.
List ofTables
jjj
-
List ofFigures
iv
1.0 BACKGROUND
1-1
1.1
Description of Wastewater Treatment Facility and Historical
Performance
1-1
1.2
Scope of Work
1-2
2.0 METHODS AND MATERIALS
2-1
2.1
Development of Preliminary Process Design
2-1
2.1.1 Alkaline Air Stripping
2-1
2.1.2 Struvite Precipitation
2-2
2.1.3 Single-Stage Biological Nitrification of Non-PC
Wastestreams Combined with Separate Biological
Treatment of the PC Wastestream
2-4
2.1.3.1
Clarification Requirements
2-4
2.1.3.2
BOD Removal Requirements
2-5
2.1.3.3
Biotreater Tankage and Oxygenation Requirements
2-6
2.1.3.4
Alkalinity Requirements
2-6
2.1.3.5
Sludge Handling Requirements
2-6
2.1.3.6 Pretreatment Requirements
2-7
2.1.4 Biological Nitrification of Combined Wastestream
2-8
2.1.5 Breakpoint Chlorination of Secondary Clarifier Effluent
2-9
2.1.6 Ion Exchange Treatment of Final Effluent
2-9
2.2
Preliminary Cost Estimates
2-10
3.0 BATCH TREATABILITY TEST RESULTS
3-1
3.1
Alkaline Air Stripping
3-1
3.1.1 pHAdjustment
3-1
3.1.2 Ammonia Removal
3-2
3.2
Struvite Precipitation
3-2
3.3
Breakpoint Chlorination of Secondary Clarifier Effluent
3-3
3.4
Ion Exchange Treatment of Final Effluent
.-
3-4
Q:\9387.O1\TS\TSTOC.DOC
i
TABLE OF CONTENTS (Continued)
Pate No.
4.0 PRELIMINARY PROCESS DESIGNAND COST ESTIMATE FOR
ALTERNATIVES
4-1
4.1
Biological Nitrification of Combined Wastestream
4-1
4.2
Alkaline Air Stripping of Secondary Clarifier Effluent
4-2
4.3
Breakpoint Chlorination of Secondary Clarifier Effluent
4-2
4.4
Comparative Analysis of Treatment Systems
4-2
Q:\9387.O
1\TS\TSTOC.DOC
U
LIST OF TABLES
-
Follows
Table No.
Title
Page No.
1-1
Summary of 1996 Wasteload
1-1
3-1
Batch Alkaline
Air Stripping Test Results
3-2
3-2
Precipitation ofStruvite from Combined Wastestream
3-2
3-3
Breakpoint Chlorination ofSecondary Clarifier Effluent
3-3
4-1
Summary of Preliminary Cost Estimate for Biological
Nitrification of Combined Wastestream
4-1
4-2
Summary ofPreliminary Cost Estimate for Alkaline Air
Stripping of Secondary Clarifier Effluent
4-2
4-3
Summary ofPreliminary Cost Estimate for Breakpoint
Chlorination of Secondary Clarifier Effluent
4-2
4-4
Effectiveness of Alternative Treatment Processes on Final
Effluent Ammonia Load Reduction
4-2
Q:\9387.O
I\TS\TSLOT.DOC
111
L!ST OF FIGURES
Follows
Figure No.
Title
Page No.
1-1
Block Flow Diagram ofWastestream Sources and WWTF
1-1
1-2
Block Flow Diagram of
Alkaline Air Stripping Treatment
Alternatives (Nos. 1, 2, and 3)
1-2
1-3
Block Flow Diagram of Struvite Precipitation Treatment
Alternative (No. 4)
-
1-2
1-4
Block Flow Diagram of Biological Nitrification Treatment
Alternative (No. 5)
1-2
1-5
Block Flow Diagram ofBiological Nitrification Treatment
Alternative (No. 6)
1-2
1-6
Block Flow Diagram of Breakpoint Chlorination Alternative
(No. 7)
1-2
1-7
Block Flow Diagram of Ion Exchange Treatment Alternative
(No.8)
-
0~
1-2
3-1
-
pH Adjustment ofPC Tank Discharge
3-1
-
3-2
pH Adjustment of PVC Tank Discharge
3-1
3-3
pH Adjustment ofSecondary Clarifier Effluent
3-1
3-4
pH Adjustment of Combined Wastestream
3-3
3-5
Clinoptiolite Treatment ofFinal Effluent for Ammonia
-
-
Reduction
34
Q:\9387.O1\TS\T$LOF.DOC
iV
1.0 BACKGROUND
1.1 DESCRIPTION OF WASTEWATER TREATMENT FACILITY AND
HISTORICAL PERFORMANCE
BF Goodrich Company (BFG) and The Geon Company (Geon) own and operate
adjoining manufacturing facilities in Henry, Illinois. Wastewaters from the BFG
manufacturing processes discharge to either the Polymer & Chemicals (PC)
equalization tank or the Cure Rite® (C-18) equalization tank. Wastewaters from
the Geon manufacturing processes and sidestreams from the combined wastewater
treatment facility (WWTF) discharge to the Polyvinyl Chloride (PVC) equalization
tank. Site-wide stormwater runoff and sidestreams from the boiler house and water
treatment facility (WTF) discharge to a holding pond (Pond). Wastewaters from the
PC Tank, C- 18 Tank, and PVC Tank are fed at controlled rates to the WWTF along
with discharge from a groundwater recovery well (Well No. 3). Pond water is
discharged at a controlled rate to either the WWTF or through a sand filter into the
channel transporting WWTF effluent to the Illinois
River. The
WWTF consists of
chemical coagulation, sedimentation, activated sludge treatment, and sand
ifitration prior to discharge to the Illinois River. The discharge is regulated by a
NPDES permit issued by the Illinois Environmental Protection Agency (IEPA). A
summary of the 1996 wasteloads is presented in Table 1-1. A block flow diagram of
the wastestream sources and WWTF is presented in Figure 1-1.
The
WWTF has historically provided greater than 95 percent BOD reduction while
discharging an effluent ammonia-nitrogen concentration of 23 to 120 mg/L.’ The
IEPA has proposed a monthly average effluent limit of 3 mg/L for ammonia (as N).
A previous study conducted by ECKENFELDER INC. in 1995 indicated that single-
stage biological nitrification was not feasible in the existing activated sludge system
due to inhibition of nitrifying bacteria caused by the PC Tank discharge. The
PC Tank discharge is also inhibitory to BOD removal by the activated sludge
process. This effect has been controlled by adjusting its flow contribution to less
than 23 percent of the combined wastestream flow and its TCOD contribution to
1,100 mg/L in the combined wastestream.
1Based on once
monthly analysis of effluent NH3-N concentrations during the period of
January 1994
through December
1996.
Q:\0387.O1\TS\TSSQ1.DOC
14
-~-~
~.——‘
.,~...—
—..-......
~
~
0’:~
TABLE
1-1
SUMMARY OF 1996 WASTELOAD
Wastestream
Flow Rate
(gpm)
SCOD (lb/day)b
TKN (lb/day)
NH3-N (lb/day)
Averagea
Peak
Average
Peak
Average
Peak
Average
Peak
PVC
Tank
Discharge
401
499
2,650
4,330
335
485
215
300
PC
Tank
Discharge
107
150
8,280
10,840
360
525
45
75
C-18
Tank
Discharge
6
15
1,320
2,940
60
150
20
50
Pond Water & Well No. 3
Discharges
46
105
50
50
2
5
1
2
Total Wastestream
560
670
12,300
14,500
757
1,165
281
427
aThe average 1995 flow rates for the PVC Tank, PC Tank, C-18 Tank, and Pond Water &
Well
No. 3 Discharges were 414, 107, 7, and
51
gpm,
respectively.
bSoluble COD defined as COD of ifitrate following 1.5
~tmfiltration.
Q:\9387.OIVFS\TSTOIOI.DOC
P~e I of I
q.~9387.Ol~ts\tsf13lOI
ppt
BLOCK FLOW DIAGRAM OF WASTESTREAM
SOURCES
AND
WWTF
ECKENFELDER I
Nashville,
Tennessee
Mahwah. New Jersey
INC.
I
Greenville. south Cerolina
Geon
~ction~4~~k
FIGURE
1-1
1.2 SCOPE OF WORK
BF Goodrich retained ECKENFELDER INC. to develop preliminary process designs
and budget level cost estimates for alternative treatment processes which would
reduce the ammonia load in the final effluent from the WWTF. The alternatives
considered are summarized below and illustrated in Figures 1-2 through 1-7.
• Alternative No. 1
-
Alkaline air stripping ofPC Tank contents
• Alternative No. 2
-
Alkaline air stripping ofPVC Tank contents
• Alternative No. 3
-
Alkaline air stripping of secondary clarifier effluent
• Alternative No. 4
-
Struvite (NH4MgPO4) precipitation from combined
wastestream influent
• Alternative No. 5
-
Single-stage biological nitrification of non-PC wastestreams
combined with separate biological treatment of the PC Tank discharge.
• Alternative No. 6
-
Biological nitrification ofcombined influent wastestream
• Alternative No. 7
-
Breakpoint chlorination of secondary clarifier effluent
• Alternative No. 8
-
Ion exchange
treatment of final effluent
Preliminary process designs were developed for each Alternative based on batch
treatability testing and wastestream characterization data gathered in previous
studies by ECKENFELDER INC., and additional treatability testing and
wastestream characterization data presented in this report. Average and maximum
daily effluent ammonia loads were projected under each alternative for the 1996
wasteload.
Preliminary cost estimates for the treatment alternatives were
developed using
preliminary process designs and information provided by vendors,
BF Goodrich, a cost estimating software program,. and ECKENFELDER INC.
The methods, results, conclusions, and recommendations of this evaluation are
presented in the following sections.
Q:\9387.O
1\T5\T5SO
I.DOC
12
Air
ALTERNATIVE NO.1 - ALKALINE AIR STRIPPING OF PC TANK CONTENTS
pvc Wastestreams) ~
~~0~~_____
~De1oarner
~iiIIXii)—~-
Sulfuric Acid
Caustic Soda
—D;;e...
To Illinois River
3To Primary Treatment)
FIGURE 1-2
BLOCK FLOW DIAGRAM OF ALKALINE
AIR STRIPPING TREATMENT ALTERNATIVES
(Nos•
1,
2, and 3)
ECKENFELDER
INC.
Nashville,
Tennessee
Mahwah, New Jersey
Greenville,
South Carolina
PVC Tank
A
‘-
I.
lulidly I pedUI,eII~,’
ALTERNATIVE NO.2-ALKALINE AIR STRIPPING OF PVC TANK CONTENTS
\
Secondary Clarifier
/ Effluent
/ ~
~ Caustic
1
I
ALTERNATIVE NO.3-ALKALINE AIR STRIPPING OF SECONDARY CLARIFIER EFFLUENT
I
Existing Equipment
--
New Equipment
q:\9387.O1’.ts\tsfOlO2.ppt
I
I Existing Equipment
r
jii
New Equipment
FIGURE 1-3
BLOCK FLOW DIAGRAM OF
STRUVITE
PRECIPITATION TREATMENT ALTERNATIVE
(No.4)
ECKENFELDER
INC.
Nashville, Tennessee
Mahwah, New Jersey
Greenville, South Carolina
NOTE: Existing FeCI3 Addition
would be discontinued
q’.9387.O1~Zs\tsfO1O3.ppt
I
I Existing Equipment
New Equipment
BLOCK FLOW DIAGRAM OF BIOLOGICAL
NITRIFICATION TREATMENTALTERNATIVE
(No.5)
ECKENFELD ER
INC.
Nashville, Tennessee
Mahwah, New Jersey
Greenville, South Carolina
FIGURE
1-4
q.~9387.O1~ls\tsfO1O4.ppt
~_00~•~00~~
~
—...~..
~
~~0~~~~00~
,0~_0...,0_...,
.00__-...0_.~..
~
~
—,.-.,00—000..
0~•_000~~_0_0~
~
I
I
Existing Equipment
New Equipment
I~
.
\‘I Upgraded Equipmemt
FIGURE 1-5
BLOCK FLOW DIAGRAM OF BIOLOGICAL
NITRIFICATION TREATMENT ALTERNATIVE
(No.6)
ECKENFELDER
INC.
Nashville, Tennessee
Mahwah, New Jersey
q:t9387.O1~s~fOlO5.ppt
Greenville, South Carolina
I
I Existing Equipment
I ~__~_i
New Equipment
FIGURE 1-6
BLOCK FLOW DIAGRAM OF BREAKPOINT
CHLORINATION ALTERNATIVE
(No.7)
ECKENFELDER
INC.
Nashville, Tennessee
Mahwah, New
Jersey
Greenville, South Carolina
q~9387.O1~Ls\tstO1O6
ppt
VSecondary Clarifier~\ ~
/
Effluent
I
Regenerant
________
I
I Existing Equipment
ETTIII
New Equipment
FIGURE
1-7
BLOCK FLOW DIAGRAM OF ION EXCHANGE
TREATMENT ALTERNATIVE
(No.8)
ECKENFELDER
Nashville,
Tennessee
Mahwah, New Jersey
INC.
Greenville, South Carolina
Filtration
Ion Exchange
Treatment
q:’~9367.O1~ls’IsfO1O7.ppt
2.0 METHODS AND MATERIALS
2.1
DEVELOPMENT OF PRELIMINARY PROCESS DESIGN
Preliminary process designs were developed based on treatment of the 1996
wasteload as described in Table 1-1. Treatment process sizing and performance
assessment assumed complete biohydrolysis of the influent TKN load to ammonia
through the activated sludge process, an influent TCBODITCOD ratio of 0.30 lb/lb,
and a TCBOD removal requirement of 0.035 lb NH3-N/lb TCBOD.
These
assumptions yielded average and peak effluent ammonia loads for 1996 of
628 lb/day and 1,013 lb/day, respectively.
The BF Goodrich WWTF has historically exhibited 50 percent to 100 percent
biohydrolysis ofthe influent TKN load. It is anticipated that this same variation in
biohydrolysis ofthe influent TKN load occurred in 1996.
2.1.1 Alkaline
Air
Stripping
“Grab type” samples of the PC Tank discharge, PVC Tank discharge, and Secondary
Clarifier Effluent were collected on April 22,
1996 and shipped
via overnight
delivery to ECKENFELDER INC.’s Laboratory in Nashville, Tennessee.
The
samples were analyzed for pH, total suspended solids (TSS), and ammonia-nitrogen
(NH3-N). Following these analyses, the samples were refrigerated until used for
subsequent testing.
The pH of the PC Tank discharge, PVC Tank discharge, and Secondary Clarifier
effluent were 12.5 s.u., 8.7 s.u., and 7.2 s.u., respectively. Alkaline air stripping of
ammonia requires an operating pH of 10 s.u. to be effective.2 The BF Goodrich
activated sludge system requires an influent pH of 9.0 to 9.5 s.u. to ensure an
operating pH of 6.5 to 7.5 s.u. The BF Goodrich effluent permit requires a discharge
pH of 6.0 to 9.0 s.u. Consequently, the pH of PVC Tank discharge and Secondary
Clarifier effluent required an increase prior to stripping and all three wastestreams
0
required a pH reduction following stripping. The caustic soda (NaOH) and sulfuric
2”Process Design Manual for Nitrogen Control,” USEPATechnology Transfer, Washington,
DC (1975).
Q:\9387.O1\TS\T3502.DoC
2 1
acid (H2S04) addition requirements to achieve the necessary pH adjustments were
determined by development oftitration curves presented in Section 3.1.
Samples of the PC Tank and PVC Tank discharges contained greater than 500 mg/L
TSS which would foul a packed tower air stripper or horizontal tray stripper.
Consequently, these wastestreams were considered fcr stripping by diffused
aeration. Due to the poor efficiency of the diffused air stripping process and the
large flow rates of these wastestreams, only stripping within the existing tankage
was considered. Construction of additional tankage to achieve improved ammonia
removal would not be cost effective. Conventional packed tower air stripping of the
secondary clarifier effluent was considered since this is the most cost-effective and
demonstrated stripping technology. The preliminary process designs of the diffused
aeration stripping processes were based on modeling by ECKENFELDER INC. The
preliminary process design of the packed tower air stripping process was developed
based
Samples
on modeling
of the PC
by
Tank
Deltadischarge,Cooling Towers.PVC
Tank3
discharge, and Secondary Clarifier
Effluent were subjected to batch diffused aeration stripping tests to confirm the
ammonia in these wastestreams was “strippable.” An aliquot (1,300 mL) of each
sample was placed in a 2,000-mL graduated cylinder and aerated using a 1-inch
porous stone diffuser at a rate of 1,000 cfm/1,000 cu ft (maximum design aeration
rate) and pH 10 s.u. The NH3-N concentration was monitored with time during
these tests and water lost to evaporation was made up with distified water. Results
of these tests indicated the ammonia was strippable and progressed at a rate
consistent with conventional theory (i.e., Henry’s Constant).
In all cases, it was assumed that the off-gas would not require collection and
treatment.
.
2.1.2 Struvite Precipitation
Grab type samples of the PC, PVC,. and C-18 Tank discharges were collected on
April 22, 1996 and shipped via overnight delivery to ECKENFELDER INC.’s
3Keith Kay of Delta Cooling Towers, Inc., 134 Clinton Road, P.O. Box 952, Fairfield, New
Jersey 07004,
(201) 227-0300.
Q:\9387.O1\’FSVFSSOS.tiOC
.
22
Laboratory in Nashville, Tennessee. The samples were blended to form combined
wastestreams to simulate the average combined influent flow rate ratio for 1995
and a combined influent containing the peak 1996 PC Tank discharge COD load
(see Table 1-1). The combined 1995 influent was analyzed for NH3-N and subjected
to three Batteries (I, II, and III) of batch treatability tests to evaluate NH3-N
removal by precipitation as struvite (NH4MgPO4).
The combined peak 1996
influent was analyzed for NH3-N and subjected to Battery IV batch treatability
tests to demonstrate the impact of PC Tank discharge contribution on test results.
Battery I, II, III, and IV batch treatability tests consisted of placing aliquots
(500 mL) of the wastestream in 1,000-mL beakers. The beaker contents were
rapidly mixed, spiked with a magnesium sulfate solution containing 10,000 mg/L
Mg~H, spiked with a phosphoric acid solution containing 10,000 mg/L P04-P,
adjusted to the desired pH using NaOH, and mixed for 60 minutes. Samples were
removed after 60 minutes, subjected to 0.45 ~imfiltration, and the filtrate analyzed
for NH3-N.
Battery I tests evaluated the impact of pH on ammonia removal while maintaining
a Mg++ dose equal to 118 percent of the stoichiometric amount required to
precipitate struvite (2.0 mg Mg~~per mg N versus 1.7 mg Mg~per mg N) and a
P04-P dose equal to 168 percent of the stoichiometric amount required to
precipitate struvite (3.7 mg P per mg N versus 2.2 mg P per mg N). Work by Arnold
and Wolfram4 indicated that excess P addition increased NH3-N removal while
excess Mg~addition did not improve NH3-N removal. Battery II tests evaluated
the impact of increased Mg~addition (3.9 mg Mg~/mgN) and P04-P addition
(7.3 mg P/mg N) on NH3-N removal while operating at a perceived optimum pH (12
to 12.5 s.u.). Battery III tests evaluated whether increased Mg~addition (2.0, 2.9,
and
3.9 mg Mg~/mgN) at a pH 9.5 s.u. would provide comparable
NH3-N
reduction to that experienced at pH of 12 s.u. and 2.0 mg Mg~/mgN while
maintaining a constant P04-P addition of 3.7 mg P/mg N. Lastly, Battery IV tests
evaluated the effect of operating pH on NH3-N
removal from the combined peak
1996 influent while providing the Mg~addition (3.9 mg Mg~~/mgN) and P04-P
addition (3.7 mg P/mg N) deemed most favorable from Battery I, II, and III tests.
4”Ammonia Removal and Recovery from Fertilizer Complex Wastewaters,” D.W. Arnold and
W.E. Wolfram,
Proceedings of 30th Industrial Waste Conference,
Purdue University, 1975.
Q:\0387.O 1\TS\TSSO2.DOC
23
In full-scale application, magnesium would be added as Sul-PO-Mag,5 and
phosphorus would be added as 85 percent (by weight, w/w) phosphoric acid
(H3P04). Primary clarifier effluent pH would continue to be maintained by addition
of 50 percent (w/w) NaOH.
2.1.3
Single-Stage Biological Nitrification of Non-PC Wastestreams
Combined with Separate Biological Treatment of the PC Wastestream
Previous work by ECKENPELDER INC. in 1995 indicated that all wastestreams at
the BF Goodrich Henry Plant (excluding the PC Tank discharge) will support
biological nitrification at their respective 1995 loads and peak 1996 loads. Further
work in 1996 and 1997 indicated that the combined wastestream was treatable for
BOD removal under the peak 1996 loads. Consequently, one alternative for effluent
ammonia reduction would be first-stage nitrification of the non-PC wastestreams
followed by a second-stage biological treatment of the PC Tank discharge after
dilution with effluent from the first-stage reactor.
Development of the preliminary process design for this treatment alternative is
described in the following subsections.
2.1.3.1 Clarification Requirements.
The peak solids loading rate (SLR) on the
secondary clarifier which the BF Goodrich WWTF has operated successfully for
weeks at a time is 29 lb MLSS/day sq ft calculated from Equation (2-1). This was
considered to be the peak allowable SLR in sizing clarification area for first-stage
and second-stage biological treatment processes.
(Qrn
+
Q~)
x
8.34
x
MLSS
2 1
SLR-
A
(-)
where:
SLR
=
solids loading rate, lb/day sq ft
= 29
lb/daysq ft (peak)
5Sul-PO-Mag
(11
percent w/w Mg), distributed by IMC Global, One Nelson C. White
Parkway, Mundelein, Illinois 60060, (847) 970-3000.
Qf\9387.OI
\TS\TSSO2.DOC
2-4
=
peak influent flow rate, MGD
Qp~
=
peak return activated sludge flow rate, MGD
MLSS
=
mixed liquor suspended solids concentration in biotreater, mg/L
A
=
clarification area, sq ft
=
2,826 sq ft for existing secondary clarifier
2.1.3.2
BOD Removal Requirements.
The required operating MLVSS
concentration for first-stage and second-stage BOD removal was calculated from
Equation (2-2)
So (So
-
Se)
XVHRT
KSe
(2-2)
where:
So
=
biotreater influent total carbonaceous biochemical oxygen
demand (TCBOD) concentration, mg/L
=
assumed equal to 0.30 x influent soluble chemical oxygen
demand (SCOD) concentration, mg/L
Se
=
final effluent SCBOD concentration, mgTL
X~
=
biomass concentration in biotreaters, mg/L MLVSS
=
assumed equal to 0.7 x MLSS concentration
HRT =
hydraulic residence time in biotreaters, days
K
=
CBOD removal rate constant, 5.2 day-i at the winter mixed liquor
temperature of 27°Cbased on 1996 treatability data
The primary clarifier effluent BOD load (S0 for first stage) was calculated by
multiplying the non-PC wastestream SCOD load (4,020 lb/day average and
7,320 lb/day peak) by the 1995 observed ratio of 0.30 lb TCBOD/Ib TCOD for these
wastestreams. The second stage BOD load was calculated by multiplying the PC
wastestream SCOD load (8,280 lb/day average and 10,840 lb/day peak) by the 1995
observed ratio of 0.30 lb TCBOD/1b TCOD. Lastly, the required HRT while
operating at the peak MLSS defined in Equation (2-1) was calculated based on
discharging effluent filtered BOD concentrations (Se) of 16 mg/L (monthly average)
and 36 mg/L (daily maximum) to comply with the monthly average and daily
maximum permit limits for effluent BOD of 20 mg/L
and 40
mg/L, respectively.
Q:\9387.O1\TS\T5302.DOC
25
This assumes that the filter effluent TSS concentration is 16 mg/L and exhibits a
BOD contribution of0.25 mg TCBOD/mg TSS.
2.1.3.3
Biotreater Tankage and Oxygenation Requirements.
Oxygen
requirements for first-stage and second-stage treatment were calculated based on
an
observed
1996
consumption
of 0.4 lb O2flb TCOD
applied
plus
4.6 lb 0211b NH3-N removed through nitrification. The existing aeration system is
capable of transferring 4,310 lb 02/day at a 2 mg/L dissolved oxygen (DO)
concentration and 31°Cand 5,050 lb On/day at a 1 mg/L DO concentration and 3 1°C.
Additional oxygen requirements beyond this capacity will be provided by addition of
biotreater tankage which is equally oxygenated since this oxygenation rate is within
14 percent of the maximum achievable with the existing diffuser type and sidewall
2.1.3.4
depth.6
Alkalinity Requirements.
Approximately 7.1 mg total alkalinity (as
CaCO3) is consumed per mg NH3-N removed during biological nitrification.
BF Goodrich currently adds NaOH to the combined influent wastestream to
maintain a minimum effluent pH of 6.5 s.u. However, quicklime rather than NaOH
would be added to the primary clarifier effluent to support the alkalinity demands
of biological nitrification due to its lower cost ($40 vs $560 per ton of alkalinity
added).
2.1.3.5
Sludge Handling Requirements.
An additional same-sized filter press
(75 cu ft) is currently needed at the BF Goodrich-Henry, Illinois Plant. This need
will become more acute with~the increased sludge production associated with
biological nitrification.
The required operating MLVSS concentration for nitrification was calculated using
Equations (2-3) and (2-4). The MLVSS calculated in Equation (2-4) was used to
calculate the clarification
area required in
first-stage treatment, assuming a
0.70 mg MLVSS/mg MLSS.
6GregWendzicki ofRoediger Pittsburgh, Inc., 3812 Route 8, Allison Park, PA 15101,
412-487-6010.
Q:\9387.O1\TS\TSSO2.DOC
2.6
1
~
(2-3)
where:
~max
=
maximum nitrification rate which can be achieved treating the
specific wastestream, 0.25 mg NH3-N/mg MLVSSnit~ers•day at
27°Cbased on 1997 treatability data
MCRT
=
mean cell residence time, days
Y
=
nitrifying biomass net yield, assumed 0.1 m MLVSS~t~ifier5/mg
NH3-N oxidized
MCRT
=
(a (CODp)
-
bXdXv
+
fSi
+
Y(NH3.Np))
(2-4)
where:
a
=
heterotrophic biomass
growth yield,
0.30 mg
MLVSS/mg CODR based on 1996 treatabifity data
CODR
COD removal through activated sludge system,
mg/day
b
=
endogenous
decay
term,
assumed
0.15 mg
MLVSS/mg degradable MLVSS day at winter mixed
liquor temperature of 27°C
Xd
=
fraction of MLVSS which is degradable, assumed
equal to 0.8/(l
+
0.2 b MCRT), dimensionless
Xv
=
MLVSS mass in biotreaters, mg
f
=
fraction of primary clarifier effluent VSS which is
non-degradable, assumed 0.5 mg/mg
Si
=
mass loading of primary clarifier effluent VSS
assuming a 30 mg/L concentration, mg/day
NH3-NR
=
NH3-N removed through activated sludge system,
mg/day
2.1.3.6 Pretreatment Requirements.
The preliminary process design for the
PC Tank discharge pretreatment system was developed based on batch treatability
testing. Quicklime (CaO) and sulfuric acid (H2S04) addition rates were based on a
Q:\9387.O1\TS\TSSO2.DOC
27
titration curve developed for the wastestream. Rapid mix and sedimentation times
were assumed to be 3 minutes and 60 minutes, respectively. Sludge quantities were
estimated based on treatabiiity data. Filter press dewatering was selected for
dewatering of the underfiow due to its demonstrated performance at the
BF Goodrich WWTF.
2.1.4 Biological Nitrification of Combined Wastestream
Previous work by ECKENFELDER INC. indicated that all non-PC Tank discharges
will support biological nitrification at their respective peak 1996 loads. Further
work indicated the PC Tank discharge would also support nitrification if pretreated
by precipitation by pH 2 and limited to a 1,000 mg/L TCOD contribution (based on
its unpretreated TCOD concentration) in the feed. Consequently, one alternative
for effluent ammonia reduction would be pretreatment of the PC Tank discharge
followed by river water addition and combined single-stage nitrification with
non-PC wastestreams. The required combined wastestream flow rate would be
900 gpm based on the 1,000 mgIL contribution limit
and peak
PC Tank discharge of
10,800 lb/day SCOD.
The required non-PC wastestream flow rate would be
750 gpm
(900
gpm
-
150
gpm). The available non-PC wastestream average flow rate
is 453 gpm. Consequently, a river water supply system would be installed which
would be capable of providing 297 gpm (750
-
453
gpm). Work completed in 1997
indicated that partial biological nitrification (?40 percent reduction in effluent
NH3-N) could be achieved in the absence of river water addition. However, river
water addition was included to maximize nitrification potential.
The same calculations described in Section 2.1.3 were used to evaluate the upgrade
measures required for oxygenation, biotreater tankage, and secondary clarification.
Secondary clarification was also limited to the peak hydraulic loading rate
sustained in 1996 (350 gpdlsq ft) due to the susceptibility of the clarifier to floc
carryover. Sand ifitration requirements were based on a peak solids loading rate of
1.0 lb TSS/day•sq ft and a peak secondary clarifier effluent TSS concentration of
50 mg/L. Same-sized secondary clarifier (60-ft diameter) and sand filter (9 ft x
24 ft) units were provided as needed.
Q:\9387.O1\TS\T5502.DOC
28
2.1.5 Breakpoint Chlorination of Secondary Clarifier Effluent
A grab type sample of the Secondary Clarifier effluent was collected on April 22,
1996 and shipped via overnight delivery to ECKENFELDER INC.’s Laboratory in
Nashville, Tennessee. The sample was analyzed for NH3-N and subjected to four
Batteries (I, II, III, and IV) of batch treatability tests. These tests consisted of
placing 500-mL aliquots in 1,000-mL beakers. The beaker contents were rapidly
mixed, spiked with a sodium hypochlorite solution (10,000 mg/L Cl2), adjusted to
the desired pH of 6.5 to 7.2 s.u. using H2S04, and mixed for a given contact time.
Samples were removed and analyzed for free available chlorine (FAC) and NH3-N.
The LTSEPA Nitrogen Control Manual suggests that the optimum pH for breakpoint
chlorinatior~is 6.5 s.u., and the BF Goodrich final effluent typically exhibits a pH of
7.2 s.u.
Battery I testing evaluated the impact of chlorine dose (0, 100, 300, and 400 mg/L
FAC) on residual NH3-N concentrations at a constant reaction pH of 6.5 s.u. and
reaction time of 5 minutes. Battery I testing indicated that 400 mgIL FAC was an
insufficient chlorine dose to provide significant NH3-N reduction and that a
5-minute óontact time was too brief to allow complete reaction with the FAC.
Consequently, Battery II testing evaluated the impact of a much higher chlorine
dose (1,000 mg/L and 2,000 mg/L FAC) and much longer contact time (60 minutes)
on residual NH3-N concentration at a constant reaction pH of 6.5 s.u. Battery II
testing indicated that a 1,300 ±100mg/L FAC dose completely oxidize all residual
NH3-N and that a shorter contact time could be provided. Battery III testing
evaluated the impact of contact time on FAC residual and confirmed whether a
1,300 mgIL ±100mg/L dose would provide complete oxidation of residual NH3-N at
a constant reaction pH of 6.5 s.u. Lastly, Battery IV testing evaluated whether
there was any difference in breakpoint chlorination performance at a reaction pH of
6.5 s.u. versus the typical BF Goodrich final effluent pH of 7.2 s.u.
2.1.6 Ion Exchange Treatment of Final Effluent
ECKENFELDER INC. developed a Freundlich isotherm for ammonia removal from
the final effluent using cinoptiolite, an ammonia selective ion exchange resin. This
isotherm was used to estimate resin usage to achieve specified effluent NH3-N
Q:\9387O1\TS\TSSO2.DOC.
29
reduction. Common design practices were used to size the ion exchange columns
(i.e., 3 gpm/sq ft).
2.2 PRELIMINARY COST ESTIMATES
Preliminary cost estimates presented in this Report were developed based on vendor
estimates, data from a commercial software program, and ECKENFELDER INC.’s
judgment. These estimates are considered accurate to within -10 percent to
+30 percent. Installed costs were based on the preliminary process design of a
system required •to treat the peak influent TKN load assuming complete
biohydrolysis of TKN to NH3-N through the activated sludge process. Annual
operation and maintenance costs also assumed complete biohydrolysis of the
influent TKN load. Present worth costs were based on a 10-year project life and an
8 percent annual interest rate.
Installed costs included construction materials and equipment plus an additional
5 percent for electrical hookup and interface instrumentation, 10 percent for
interface piping and site work, 15 percent for contingency, and 30 percent for
engineering, general contracting, permitting, and project administration.
Operation and maintenance costs considered only labor and chemical usage. The
cost of labor was assumed as $30/hour. The cost of chemicals were as follows:
$350/ton of 50 percent NaOH, $90/ton of 93 percent H2S04, $750/ton of 75 percent
H3P04, $110/ton of Sul-PO-Mag, $200/ton of chlorine gas, $70/ton of 90 percent
CaO, and $35/l00 lb of sodium bisulfite. Costs for maintenance materials and
electricity were not included in the estimate.
Q:\9387.Qi\TS\TS$02.DOC
2-10
3.0 BATCH TREATABILITY TEST RESULTS
ECKENFELDER INC. conducted batch treatability tests to assess the feasibility of
treatment alternatives discussed in Sections 1.0 and 2.0. Results from these tests
were used to develop preliminary process designs for those treatment alternatives
deemed feasible. The results are described in the following subsections.
3.1 ALKALINE AIR
STRIPPING
3.1.1 pH
Adjustment
The PC Tank discharge, PVC Tank discharge and secondary clarifier effluent
required pH adjustment to provide alkaline air stripping for ammonia removal and
subsequent discharge.
The pH adjustment requirements of these three
wastestreams are illustrated in Figures 3-1, 3-2 and 3-3 and are discussed below.
The quantity of 93 percent by weight (w/w) H2S04 required to lower the PC Tank
discharge pH (10.6 s.u.) to that required for discharge to the biotreaters (pH 9.25 ±
0.25 s.u.) is 5 lb/1,000 gallons. Consequently, the average and peak usage of
93 percent H2S04 in 1996 would have been 770 lb/day and 1,080 lb/day,
respectively.
The quantity of 50 percent, w/w, NaOH required to elevate the PVC Tank contents
from pH 8.3 s.u. to pH 10.5 for stripping is 70 lb/1,000 gallons. At the average and
peak day flow rates of 401 gpm and 499 gpm, the required daily quantities of
50 percent NaOH would have been 40,400 lb/day and 50,300 lb/day, respectively.
The quantity of 93 percent H2S04 required to lower the pH from 10.5 s.u. after
stripping to that required for discharge to the biotreaters (pH 9.25 ±0.25 s.u.) is
4 lb/1,000 gallons. The average and peak quantities of 93 percent H2S04 required
would have been 2,310 lb/day and 2,870 lb/day, respectively.
The quantity of 50 percent NaOH required to elevate the secondary clarifier effluent
from pH 7.8 s.u. to pH 10.5 is 7.5 lb/i,000 gallons. At average and peak day flow
rates of 560 gpm and 670 gpm, the daily quantities of 50 percent NaOH required
would have been 6,050 lb/day and 7,240 lb/day, respectively. The quantity of 93
percent H2S04 required to lower the pH to 8.5 s.u. to ensure effluent permit
Q:\9387.O1\TS\TS$03.DOC
31
60
3.0
4.0
pH, s.u.
7.0
8.0
9.0
10.0
11.0
Figure 3-1 pH Adjustment of PC Tank Discharge
55
0
50
45
~40
~35
.—
.—
~25
~20
15
10
5
0
50 NaOH
• 93 H2S04
0
2.0
5.0
6.0
q~\93~7.OPd$\TSJ’O3.XLS
155
150
145
140
135
130
125
120
115
110
4:
C
95
C
~80
4
75
~70
~65
C,
Ci)
~55
6.0
7.0
11.0
12.0
pH, s.u.
Figure 3-2 pH Adjustment of PVC Tank Discharge
8.0
9.0
10.0
0 50
NaOH
• 93H2S04
0
q:\9387.OI’.u\TSFO3.XLS
17
16
15
14
13
12
0
________________
—
C
C
C
‘-4
Ca
—9
.—
0
-‘I
C,7
1;
4
3
2
5.0
6.0
10.0
11.0
12.0
pH, su.
Figure 3-3 pH Adjustment of Secondary Clarifier Effluent
7.0
8.0
9.0
0 50 NaOH
• 93
H2S04
0
1
0
q;\93i7.OI\uVtSI’O~7~5S
~r
compliance (~pH9.0 s.u.) would have been 3.0 lb/1,000 gallons, or 2,420 lb/day
average and 2,890 lb/day, peak.
3.1.2
Ammonia
Removal
Batch alkaline air stripping test results for the three wastestreams are presented in
Table 3-1. These results indicate that the NH3-N present in these wastestreams
can be removed through alkaline air stripping.
Modeling conducted by
ECKENFELDER INC. indicated that 80 percent (36 lb/day) of the 1996 average
NH3-N load discharged from the PC Tank could be removed by in situ aeration of
the Tank contents at pH 10.6 and a rate of 100 cfm/1,000 cu ft.
Likewise,
60 percent (129 lb/day) of the 1996 average i.., 3-N load discharged from the PVC
Tank could be removed by aerating the Tank contents at this same rate and at a pH
of 10.5 s.u. These removal rates are ~21 percent of the 1996 average final effluent
NH3-N load of 628 lb/day assuming complete biohydrolysis of the influent TKN.
The low removals are due to the fact that the average influent NH3-N load which
can be removed at these two equalization tanks comprises only 34 percent of the
average influent TKN load in which all TKN is assumed to be biohydrolized to
N113-N through the activated sludge process. The 1996 average final effluent
NH3-N load could be reduced by 95 percent by alkaline air stripping of the
secondary clarifier effluent. This higher rate ofremoval is possible since it has been
assumed that all of the influent TKN load is biohydrolized by the activated sludge
process and is, therefore, available for stripping from the final clarifier effluent.
The secondary clarifier effluent is the most effective application point for alkaline
air stripping.
3.2 STRUVITE PRECIPITATION
Batch treatability tests evaluated precipitation of struvite (NH4MgPO4) from the
combined wastestream. Results of these tests are summarized in Table 3-2.’ They
indicate that the combined wastestream NH3-N concentration can be reduced to
approximately 25 mg/L under two operating conditions.
• A magnesium dose of 2.0 mg Mg/mg N, phosphorus dose of 3.7 mg P/mg N
and an operating pH of 10.5 to 12.5 s.u.
Q:\9387.O1\TS\TSSO3.DOC
32
TABLE
3-1
BATCH
ALKALINE AIR
STRIPPINGTEST RESULTS
Wastestream
Time of Aeration at
100 cfmll,000 Cu ft
(days)
Reaction pH
(s.u.)
NH3.N
Residual
(mg/L)
NH3.N
Removala
(lb/day)
PC Tank Discharge
0
0.1
1.0
2.0
3.0
7.0
12.5
12.5
12.5
12.5
12.5
12.5
23
19
4
4
4
3
0
5
24
24
24
26
PVC Tank Discharge
0
1.0
2.0
6.0
10.0
10.0
10.0
10.0
50
44
25
6
0
29
120
210
Secondary Clarifier Effluent
0
1.0
2.0
3.0
6.0
10.0
10.0
10.0
10.0
10.0
100
70
43
28
6
0
200
380
480
630
aBased on average 1996 flow rates for PC Tank discharge, PVC Tank discharge, and final effluent of 107
gjm,
401 gpm, and 560 gpm, respectively.
Q~’9387.O1\TS\TSTO3O1.DOC
Page 1 of 1
TABLE
3-2
PRECIPITATION OF STRUVITE FROM COMBINED WASTESTREAM
Test
Magnesium Addition
Phosphorus Addition
NaOH Addition
Reaction
pH
Filtered
NH3-N
NH3-N
Battery
Doseb
Dose
Dosec
Doseb
Dose
Dosec
Dose
Dosec
Removaic
No.a
()
(mg/L as Mg)
(lb/day)
()
(mg/L
as P)
(lb/day)
(meq/L)
(lb/day)
(s.u.)
(mgIL)
(lb/day)
1995
Wastestream
I
0
0
0
0
0
0
0
0
10.0
41
0
114
80
4,860
166
150
3,730
0
0
8.0
37
27
114
80
4,860
166
150
3,730
2.2
1,180
8.5
35
41
114
80
4,860
166
150
3,730
5.8
3,130
9.0
35
41
114
80
4,860
166
150
3,730
10.4
5,600
9.5
32
61
114
80
4,860
166
150
3,730
14.6
7,860
10.0
32
61
114
80
4,860
166
150
3,730
20
10,800
10.5
24
113
114
80
4,860
166
150
3,730
22
11,800
11.0
29
81
114
80
4,860
166
150
3,730
37
19,900
11.5
20
-
139
114
80
4.860
166
150
3,730
43
23,200
12.0
26
104
114
80
4,860
166
150
3,730
89
47,900
12.5
21
139
II
229
160
9,810
333
300
7,470
59
31,800
12.0
25
104
229
160
9,810
333
300
7,470
105
56,500
12.5
20
139
III
114
80
4,860
166
150
3,730
9.4
5,060
9.5
35
41
171
120
7,380
166
150
3,730
9.6
5,170
9.5
28
76
229
160
9.810
166
150
3,730
9.6
5,170
9.5
25
104
Peak 1996
Wastestream
IV
0
0
0
0
0
0
0
0
10.5
34
0
229
160
9,810
166
150
3,730
5.0
2,690
9.5
28
41
229
160
9,810
166
150
3,730
15
8,070
11.5
23
74
aTest Battery Nos. I, II, and III considered treatment of the 1995 average influent and Test Round No. IV considered treatment of the peak 1996 influent.
bPercent ofstoichiometric dose added.
CBased on 560
gpm
flow
rate.
Q:\9387.O1\TS\TSTOSO2 Doe
Poge
I
of
I
• A magnesium dose of 3.9 mg Mg/mg N, phosphorus dose of 4.1 mg P/mg N
and an operating pH of 9.5 s.u.
The second condition is less costly. It substitutes 4,950 lb/day more Sul-PO-Mag
($270/ton) for 5,630 lb/day less 50 percent NaOH ($350/ton). It also eliminates the
need for the 5 lb/1,000 gallons of 93 percent H2S04 required to lower the pH from
10.5 s.u. to 9.5 s.u. prior to discharge to the biotreaters (See Figure 3-4).
This treatment process is feasible, but would have provided only a 17 percent
reduction (105 lb/day) in the average final effluent NH3-N load projected for 1996.
This low removal rate is due to the fact that the average influent NH3-N load
comprises only 37 percent ofthe average influent TKN load and, as such, the bulk of
the potential effluent nitrogen load is not yet available for removal at this point in
the treatment system.
3.3
BREAKPOINT CHLORINATION
OF SECONDARY CLARIFIER
EFFLUENT
Batch treatability testing of breakpoint chlorination used sodium hypochlorite
(NaOCl). Sulfuric addition was required to maintain the desired reaction pH of 6.5
to 7.2 s.u. during the tests. Due to the large quantity of chlorine that would be
required, chlorine gas (and not NaOC1) would be used in the full-scale application.
Treatability testing indicated that chlorination of the Secondary Clarifier effluent
caused a net increase in alkalinity since NaOCl was used. However, a net decrease
in alkalinity would be experienced in full-scale application with chlorine gas
addition, and 12.0 lb NaOH per lb NH3-N oxidized would be required to maintain a
target pH of 6.9 ±0.3s.u. At average and peak effluent ammonia loads of 628 lb/day
and 1,013 lb/day, the average and peak addition rates of 50 percent NaOH would
have been 15,100 lb/day and 24,300 lb/day, respectively. Excess chlorine would be
quenched using 1.4 lb sodium bisulfite (NaHSO4) per lb chlorine reduced. Post
aeration would be provided downstream of NaHSO4 addition to quench residual
bisulfite.
Results of the batch treatability tests are summarized in Table 3-3. They indicated
that the secondary clarifier effluent exerted a background chlorine demand of
130 mg/L and required 7.8 mg Cl~/mgNH3-N oxidized.
This is in excellent
Q:\9387.O1\TS\’I’5503DOC
33
75
70
65
60
55
Cl)
~5o
~ 45
I-
Cl)
—
0
Ca
25
20
15
10
5
0
o
50NaOH
93 H2S04
7.0
8.0
9.0
10.0
11.0
pH, s.u.
12.0
Figure 3-4 pH Adjustment of Combined Wastestream
13.0
q:\9301OI\Is\TSFO3.XI.S
TABLE
3-3
BREAKPOINT CHLORINATION OF SECONDARY CLARIFIER EFFLUENT
Test
Chlorine Addition
Reaction
Time
FAC
Reaction
pH
H
Dose
2S04
NH3-N
Battery
Dose
Dosea
Residual
Removala
No.
(mgIL)
(lb/day)
(mm)
(mgIL)
(s.u.)
(meqIL)
(mgIL)
(lb/day)
10
100
300
400
0
680
2,020
2,690
0
5
5
5
0
6
17
16
7.2
6.5
6.5
6.5
0
1.6
2.2
4.6
138
110
110
120
0
190
190
120
2
1,000
2,000
6,770
13,500
60
60
5
51
6.5
6.5
6.6
17.6
27
1.4
750
920
3
1,200
1,200
1,200
1,200
1,400
8,070
8,070
8,070
8,070
9,460
15
30
45
60
60
.
10
8
6
6
106
6.5
6.5
6.5
6.5
6.5
4.6
4.6
4.6
4.6
8.2
NAb
NA
NA
1.5
0.23
NA
NA
NA
920
930
4
1,200
8,070
45
8
7.2
2.5
1.3
920
aBased on 560
gpm
flow rate, chlorine gas addition, and 93 percent w/w H2S04 addition.
bNot analyzed.
Q:\938701\TS\TSTOSO3DOC
Page 1 of I
agreement with the stoichiometric value of 7.6 mg Cl~/mgNH3-N oxidized.
Furthermore, the results indicated that near complete destruction of final effluent
NH3-N was
achieved at an operating pH of 6.5 s.u. to 7.2 s.u. and a 60-minute
contact time.
Breakpoint chlorination would have provided 97 percent reduction in the 1996
average final effluent NH3-N
load.
This is the best removal performance achieved
by any ofthe treatment alternatives considered.
3.4 ION EXCHANGE TREATMENT OF FINAL EFFLUENT
Batch treatability tests evaluated treatment of the secondary clarifier effluent using
cinoptiolite, an ammonia selective ion exchange resin. Results of this work are
illustrated in Figure 3-5. They indicate that greater than
50 lb of cinoptiolite
would be required to remove each 1 lb of
NH3-N at residual N113-N concentrations
less than 100 mg/L. This poor removal efficiency is presumed to be due to the large
concentration of competing cations in the effluent. The total dissolved solids
concentration of the final effluent is typically 8,500 ±1,500mg/L. This treatment
alternative would provide near complete
NH3-N
removal.
However, the
impracticality of adding and regenerating this quantity of cinoptiolite precluded
further consideration ofthis alternative.
Q:\9387.O1\TS\TSSO3.DOC
3-4
1
Residual
NH3-N
Concentration,
mg/L
Figure 3-5
Clinoptilolite Treatment of Final Effluent for
Ammonia
Reduction
I
E
0.1
0.01
0.001
7
I
/
I
I-
/
/
.,
10
100
q:\0387.Ol\
(.i\TSFO3.XT..S
4.0 PRELIMINARY PROCESS DESIGN
AND
COST ESTIMATE FOR
ALTERNATIVES
Only three alternatives were both practicable and capable of providing greater than
a 25 percent reduction in the average effluent ammonia load (628 lb/day) and
greater than 65 percent removal in the peak effluent ammonia load (1,013 lb/day)
projected for 1996. These were, in descending order of effectiveness: Biological
nitrification of the combined wastestream, alkaline air stripping of secondary
clarifier effluent, and breakpoint chlorination of secondary clarifier effluent. Block
flow diagrams for these Alternatives were presented in Figures 1-5, 1-2, and 1-6,
respectively.
4.1 BIOLOGICAL NITRIFICATION OF COMBINED WASTESTREAM
Biological nitrification of the combined wastestream will require a pretreatment
system for the PC Tank discharge, additional biotreater tankage, and additional
aeration equipment. The required oxygenation capacity is 10,500 lb O~/dayto
satisfy the 1996 peak TCOD and TKN loads. This treatment capacity would be
satisfied by providing an additional 1.5 MG of equally oxygenated biotreater
volume.
The system would likely provide a 95 percent reduction in the average effluent
ammonia load. The effluent ammonia load associated with the peak day TKN load
(an additional 385 lb/day) could be nitrified if the load were preceded by a gradual
increase or could “pass through” if it were associated with a sudden increase.
Oxygenation and alkalinity addition capacities must, therefore, be capable of
supporting nitrification ofthe peak day TKN load.
In addition to biotreater tankage, the peak flow required to provide adequate
dilution for uninhibited nitrification is 300 gpm.
This additional flow will
necessitate a river water supply system, additional secondary clarifier, additional
sand filter, additional RAS pumping capacity, and reworking of WWTF piping. A
summary of the preliminary cost estimate for these upgrades is provided in
Table 4-1.
Q:\9387.O1\TS\T5S04.DOC
44
TABLE
4-1
SUMMARY OF PRELIMINARY COST ESTIMATE FOR
BIOLOGICAL NITRIFICATION OF COMBINED WASTESTREAM
Description
O&M
Installed
Cost
($)
Present
Worth
($/~)
($)a
($)
Pretreatment System
SulfuricAcid Addition System
Quicklime Addition System
2-Stage Rapid Mix Before Sedimentation
S
Flocculation
Sedimentation
.
Rapid Mix After Sedimentation
Filter Press for Sludge Dewatering
Sitework, Piping, Instrumentation, Electrical
Biological Treatment
300 gpm River Water Supply System
.
Additional 1.5 MG in Biotreater Tankage
Additional 6,200 lb 02/day Transfer Capacity
Additional 60 ft diameter Secondary Clarifier
.
Additional
9 ft x 24
ft Sand Filter
Additional 300 gpm RAS pumping capacity
Additional 75 cu ft filter press
Sitework, Piping, Instrumentation, Electrical
0
0
3,900,000
3,900,000
Sulfuric
Acid (4,950 lb/day of 93
H2S04)
81,300
546,000
0
546,000
Quicklime (4,000 lb/day of 90 CaO)
51,100
343,000
0
343,000
Labor (24 hr/day)
263,000
1,765,000
0
1,765,000
395,400
2,654,000
3,900,000
6,554,000
aCosts expressed in February 1997 dollars. Assumes 10-year project life at
8
percent interest and no
salvage value.
bApproximately $1,500,000 in capital and $2,000,000 in present worth would be saved if no river
water addition were provided since the river water supply system, additional secondary clarifier,
additional sand filter, and additional RAS pumping capacity would not be required.
Q:\9387.O1\TS\TSTO4O1.flOC
Page 1 of 1
4.2 ALKALINE AIR
STRIPPING
OF SECONDARY CLARIFIER EFFLUENT
Secondary clarifier effluent would discharge by gravity at a year-round temperature
of~25°Cthrough a pH adjustment step to raise the pH to 10.5 s.u. The pH adjusted
effluent would discharge to a wet-well and be pumped to packed tower air strippers.
The discharge from the air strippers would flow by gravity through pH
neutralization (reduction to pH 8.5 s.u.) and then to the existing sand filters. The
system would likely provide a 95 percent reduction in effluent ammonia load. A
summary of the preliminary cost estimate for this system is provided in Table 4-2.
4.3
BREAKPOINT
CHLORINATION OF SECONDARY CLARIFIER EFFLUENT
Secondary clarifier effluent would discharge by gravity to a completely mixed
reaction tank. Chlorine gas would be sparged into the tank and caustic soda would
be added to the tank contents to maintain a target pH of 6.9 ±0.3 s.u. Effluent
from the reaction tank would discharge into a second completely mixed reaction
tank into which sodium bisulfite would be added to quench residual chlorine (as
needed). Lastly, the effluent would discharge by gravity to a post aeration tank to
quench residual bisulfite and then to the existing sand ifiters.
This treatment system is capable of providing the greatest effluent NH3-N
reduction of the three alternatives discussed in this Section (likely a 97 percent
reduction). A summary of the preliminary cost estimate for this system is provided
in Table 4.3
4.4 COMPARATIVE ANALYSIS OF TREATMENT SYSTEMS
The projected effluent quality, reliability, and costs of the three alternative
S
treatment systems were compared. Results ofthis comparison are provided below.
SS
SS
All three treatment alternatives are capable of providing at least a 95 percent
reduction in the average effluent N113-N load. Breakpoint chlorination wifi provide
the lowest achievable effluent ammonia concentration of the three treatment
alternatives. However, effluent alkaline air stripping and breakpoint chlorination
could increase effluent aquatic toxicity due to alteration of effluent constituents
and/or an increase in effluent TDS (~1,300mg/L).
Q:\9387.O 1\TS\TSSO4.DOC
42
TABLE
4-2
SUMMARY OF PRELIMINARY COST ESTIMATE FOR
ALKALINE AIR
STRIPPING OF SECONDARY CLARIFIER EFFLUENT
Description
O&M
Installed
Cost
($)
Present
Worth
($/yr)
($)a
($)
Sodium Hydroxide Addition System
SulfuricAcid Addition System
2-Stage Rapid Mix before Wet Well
Wet Well and Pumping Station
Packed Tower Air Strippers
2-Stage Rapid Mix after Strippers
S
Piping, Instrumentation, Electrical
0
0
2,100,000
2,100,000
Sulfuric Acid (2,420 lb/day of 93 H2SO4)
39,800
267,000
0
267,000
Sodium Hydroxide (6,050 lb/day of 50 NaOH)
386,000
2,590,000
0
2,590,000
Labor (8 hr/day)
88,000
590,000
0
590,000
513,800
3,447,000
2,100,000
5,547,000
aCosts expressed in February
1997
dollars. Assumes 10-year project life at 8 percent interest and no
salvage value.
(~:\9387.O1\TS\TSTO4O2.DOC
Page 1 of 1
TABLE
4-3
SUMMARY OF PRELIMINARY COST ESTIMATE FOR
BREAKPOINT CHLORINATION OF SECONDARY CLARIFIER EFFLUENT
Description
S
O&M
Installed
Cost
($)
Present
Worth
($/yr)
($)a
(~)
Sodium Hydroxide Addition System
9,000 lb/day Chlorinator
2-Stage Reaction Tank (60 mm HRT)
Sodium Metabisulfite Addition System
Reaction Tank (15 mm HRT)
Post Aeration Tank (15 mm HRT)
S
Aeration System
Piping, Instrumentation, Electrical
.
0
0
1,700,000
1,700,000
Chlorine Gas (5,770 lb/day)
210,600
1,413,000
0
1,413,000
Sodium Hydroxide (15,100 lb/day of 50 NaOH)
964,500
6,472,000
0
6,472,000
Sodium Bisulfite (30 lb/day of NaHSO3)
3,800
25,000
0
25,000
Labor (8 hr/day)
88,000
590,000
0
590,000
1,266,900
8,500,000
1,700,000
10,200,000
aCosts expressed in February 1997 dollars. Assumes 10-year project life at 8 percent interest and no
salvage value.
S~5S
1S~SSS
S
Q:\9387.Ol\TS\T5T0403.DOC
Page 1 of I
Biological nitrification is the least reliable of the three treatment processes since it
is most susceptible to process upsets and requires the longest process recovery.
These upsets may be caused by improper pH and DO maintenance, slug loading
and/or bioinhibitory compounds present in the wastewater. Alkaline air stripping
has the next lowest reliability since its performance is affected by ambient air
temperatures, scaling of the media, and fouling of the media related to elevated
levels of effluent TSS. Breakpoint chlorination is the most reliable of the three
treatment ?.lternatives. Its effectiveness is a function of chlorine dose and operating
pH, both ofwhich are controllable.
-
The three alternatives have present worth costs that vary from $4,554,000 for
biological nitrification of combined wastestream without river water addition to
$10,200,000 for breakpoint chlorination (see Table 4-4). The treatment alternative
with the next lowest present worth cost was alkaline air stripping ($5,547,000). In
addition, alkaline air stripping has the lowest NH3-N removal cost ($2.55/lb NH3-N
removed).
Q:\9387.O1\TS\TSSO4.DOC
43
TABLE 4-4
EFFECTIVENESS OF ALTERNATIVE TREATMENT PROCESSES ON
FINAL EFFLUENT AMMONIALOAD REDUCTION
Treatment Process
Present Worth
Cost
($1,000)
Average NH3-N
Removala
(lb/day)
NH3-N Removal
Costb
($flb)
Combined Wastestream Nitrification
With River Water Addition
Without River Water Addition
6,554
4,554
595
—420
3.02
2.97
Alkaline Air Stripping of Secondary
Clarifier Effluent
5,547
595
2.55
Breakpoint Chlorination ofSecondary
Clarifier Effluent
S
10,200
610
4.58
aAssumes complete biohydrolysis of influent TKN load to NH3-N through the activated sludge
process.
bEased on removal during 10-year period of present worth analysis.
Q:\9387.O
1\TS\TSTO4O4.DOC
Page 1 of
7
BROWN
AND
CALD WELL
MEMORANDUM
TO:
Mark Latham, Esq.
JOB NO:
27-21522.001
FROM:
T.
Houston Flippin, P.E., DEE
DATE:
May 17, 2002
SUBJECT:
Ammonia-Nitrogen Treatment Alternatiyes
Support Exhibit
Sc
Brown and Caldwell is providing
below a
summary of information intended to support the
discussion of ammonia-nitrogen (NH3-N) treatment alternatives described in the Petition For
Adjusted Standard. This information is the product of treatability testing, full-scale plant testing,
and data provided by the Noveon-Henry Plant staff.
In order to develop treatment alternatives, a “design influent and effluent wasteload” was required.
This wasteloads were developed based on individual wastestream data gathered in 1995 and effluent
data gathered in 1999 through 2000 and are summarized below in Tables 1 and 2. A flow schematic
is provided in Attachment A of the wastewater treatment facility (W\~VTF)provided at the Henry
Plant.
Table 1. InfluentWasteload Used In Developing Treatment Alternatives
Parameter
PVC Tank
PC
Tank C-18 Tank
Holding Pond/
Well No. 3 Waters
Total
Flowrate, gpm
Average
Peak
401
499
107
150
6
15
46
105
560
769
SCOD, lbs/day
Average
Peak
2,650
4,330
8,280
10,840
1,320
2,940
50
12,300
18,160
Estimated BOD, lbs/day
Average
Peak
795
1,300
S
2,485
3,250
395
880
15
15
3,690
5,445
TKN, lbs/day
Average
Peak
459
640
494
693
82
198
3
7
1038
1537
NH3-N, lbs/day
Average
Peak
295
411
62
87
27
66
S
1
3
385
571
P:\PROJ\21522\M051702 Latham.doc
Memorandum to Mark Latham, Esq.
May 17, 2002
Page 3
A summary of conceptual level operations and maintenance costs for each of these alternatives are
summarized in Table 4. The total costs presented in this table are considered accurate to within
±30 percent.
Table 4. Annual Operating
and Maintenance Cost Estimates For Treatment Alternatives
Cost Components
Annual O/M Costs in
$
Thousands
Treatment Alternative Number
for
1
2
3
4
5
6
7
8
910
Labor ($40/hour)
Electrical ($0.06/kwh)
Natural Gas ($0.06/therm)
Chemicals (Plant Costs)
Resin Replace.
($35/cu
ft~
Off~siteDisposala
Maintenance Materialsb
32
64
18
0
0
0
17
32
29
0
1,794
0
0
2
60 8
60 60 60
214
0
4
10
98
0000
0
575
642 1,028
218
788
00000
00000
105
1
19
11
45
60
10
0
147
242
51
14
30
1,363
0
226
0
0
115
60
88
0
459
0
0
22
Sub-total
Contingency (10
)
Total Annual
130
13
143
1,858
186
2,044
954
652 1,111
299
990
524 1,735
629
95
65
111
30
99
52
173
63
1,049 717
1,222
329
1,089 576
1,908
692
a
Cost of disposing of spent regenerant containing 29.7
percent by weight NH4CI (8 percent N)
assumed to be $0.10/gallon.
b Based on 5 percent of equipment costs.
A comparison of alternatives regarding present worth costs and ammonia removal is provided in
Table 5.
Table 5. Comparison of Present Worth Costs andAmmonia Removal for Treatment Alternatives
Components
Treatment Alternative Number
1
2
3
4
5
6
7
8
9
10
NH3-NRemoval,lbs/day
NH3-NRemoval,
Present Worth Costs
247
27
147
16
864
95
217
24
891
98
423
47
891
98
891
98
891
98
891
98
•
Capital
• O/M~
1.35
0.96
0.34
13.71
6.98
7.04
0.25
4.81
1.53
8.20
2.68
2.20
4.40
7.31
1.20
3.87
7.52
12.80
6.76
4.64
•
Total
2.31
14.06 14.02 5.06
9.73
4.88 11.71 5.07 20.32
11.41
a
Based onlO year period, 8 percent annual interest, and no salvage value.
P:\PROJ\2
522\MO51
702 Latham.doc
ATTACHMENT A
ILLUSTRATION OF AMMONIA-NITROGEN
TREATMENT ALTERNATIVES
May 17,
2002\00027\P:\PROJ\21522\ATTAcFIMENT A.doc
FIGURE 1
BLOCK FLOW DIAGRAM OF WASTESTREAM
SOURCES AND WWTF
BROWN AND
PJPROJ/21522/Fig1
C A L D
w
E L L
Nashville
Tennessee
Off-Gas
Treatment
Air
—
To Primary
S
Treatment
ALTERNATIVE NO.1 - ALKALINE AIR STRIPPING OF PC TANK CONTENTS
~~testream~-~
Caustic Soda
PVC Tank
‘~‘—
To Primary
Defoamer
Treatment
Air
Sulfuric Acid
S
ALTERNATIVE NO.2 - ALKALINE AIR STRIPPING OF PVC TANK CONTENTS
S
Off-Gas
Effluent
Acid
Pcwer
Treatment
ALTERNATIVE NO.3
-
ALKALINE AIR STRIPPING OF SECONDARY CLARIFIER EFFLUENT
FIGURE 2
BLOCK FLOW DIAGRAM OF ALKALINE
AIR STRIPPING TREATMENT ALTERNATIVES
Existing Equipment
(Nos. 1, 2, and 3)
New Equipment
BROWN
AND
P:/PROJ/21522iFig 2
________
-
-
C A L
L L
Nashville, Tennessee
~~nedInfluen~.—~j
pH Adjustment
‘-9i~
Coagulation
Sedimentation
I
To_Biotreater1~
Magnesium
S
To Filter_Pre~~
Phosphoric Acid
~icSod~
~nicPoIym~
NOTE: Existing FeCI3 Addition would be discontinued
S
‘ Existing Equipment
New Equipment
S
FIGURE 3
BLOCK FLOW DIAGRAM OF STRUVITE
PRECIPITATION TREATMENT ALTERNATIVE
(No.4)
S
BROWN
AND
S
A
~
~,
r
Nashville, Tennessee
P:/PROJ/21522/Fig3
-‘
~-‘
L’
TV
L, L~
L~
Reaction
Filtration
To Illinois River
Chlorine Gas
Backwash
Caustic Soda
Existing Equipment
New Equipment
S
FIGURE
4
BLOCK FLOW DIAGRAM OF BREAKPOINT
CHLORINATION ALTERNATIVE
S
(No.5)
BROWN
AND
S
C A L D ~ E L L
Nashville,Tennessee
P:IPROJI21
522/Fig 4
Quicklime
C-18 Tank
PC Tank
Coagulation
“*
Sedimentation
Sulfuric Acid
Anionic Polymer
Sedimentation
I
Sedimentation
Existing Equipment
New Equipment
FIGURE 5
BLOCK FLOW DIAGRAM OF NON-PC WASTESTREAM
NITRIFICATION TREATMENT ALTERNATIVE
BROWN AND
ALD WELL
(No.6)
P:IPROJ/21522/Fig 5
55~
River Water.
CTan~~
Sulfuric Acid
Coagulation
S
Sedimentation
Anionic Polymer
Quicklime
Existing Equipment
New Equipment
IS
S
Upgraded Equipment
FIGURE 6
BLOCK FLOW DIAGRAM OF COMBINED WASTESTREAM
NITRIFICATION TREATMENT ALTERNATIVE
(No.7)
BROWN AND
CALD WELL
Dewatering
To Landfill
P:/PROJ/21522!Fig 6
Caustic
Soda
S
Regenerant
S
~~..Secondar~
CIar~~
~
Filtration
I—*i
Ion Exchange
——~inoisRive~-
Spent Regenerant
S
To
Off-Site Disposal
I
I
Existing Equipment
New Equipment
S
FIGURE 7
S
BLOCK FLOW DIAGRAM OF ION EXCHANGE
TREATMENT ALTERNATIVE
(No.8)
BROWN AND
C A L D W E L L
Nashville, Tennessee
P:/PROJ/21522/Fig
7
I~SecondarY Clari~~ ~
Filtration
I—~’ Treatment
~IinoisRive~’-
Caustic Soda
I
1 Existing Equipment
New Equipment
FIGURE 8
BLOCK FLOW DIAGRAM OF OZONE
TREATMENT ALTERNATIVE
(No.9)
-
S
BROWN
AND
C A L D W E L L
Nashville, Tennessee
P:/PROJ/21522/Fig
8
Caustic Soda
Air
~
N~:~n ;..~J
Filtration
J~~linois
River
Existing
Equipment
-
!
New Equipment
S
FIGURE 9
BLOCK FLOW DIAGRAM OF TERTIARY
NITRIFICATION TREATMENT ALTERNATIVE
(No. 10)
BROWN
AND
C A L D ~ E L L
Nashville,Tennessee
P:/PROJ/21522/Fig
9
8
BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
OF THE STATE OF
ILLINOIS
IN THE MATTER OF:
)
)
Petition ofNoveon, Inc.
)
)
ASO2-____
)
(Adjusted Standard)
for an Adjusted
Standard
from
)
35
HI.
Aclrn. Code 304.122
)
AFFIDAVIT
OF DAVID
E. GIFFJN
I, David E. Giffin, being duly sworn and upon
oath,
state as follows:
1.
1 am the Health, Safety and Environmental Manager at the Noveon Henry Plant.
2.
In that position, I have personal knowledge ofthe facts set forth in the attached
Petition for Adjusted Standard.
3.
1-laying read the facts presentedtherein, I hereby state that to the best of my
knowledge and belief the material facts set forth therein are true and accurate.
FURTHERA~FIANTSAYETH
NOT
H
___________
., ~
,.
DAVID E.
GIFF~
U~U~~L
~•~j~’
..,
NOVEON, iNC.
~
LESU~E
A
D~’~R ~
~ ~OTAI~Y
~
~. ~~‘(vrE
Rjjy~)is
~‘W
C~.
~
~
I
1i’c~i~..i
I
(1)au~
Of4~a~q
Notary Public
S
CHO1/12226804.1
S
)K*
TC~TP! P~F~ **