1. 28-88
      2. 28-89
      3. 28-91
      4. 28-94
      5. 28-95
      6. 28-96
      7. 28-97
      8. 28-99
      9. 28-1 01
      10. 28-1 02

ILLINOIS POLLUTION CONTROL BOARD
October
13,
1977
IN THE MATTER OF:
PROPOSED AMENDMENTS TO
)
R75-9,
R76-8, -12, —13
CHAPTER
2: AIR POLLUTION,
)
(CONSOLIDATED)
RULE 206:
CARBON MONOXIDE
ORDER OF THE BOARD
(by Mr. Goodman):
The following are hereby adopted as
a proposed final draft
Opinion and Order of the Board
in this matter.
The proposed final
draft Order shall be set for publication and a 45—day public
comment period.
The Proposed final draft Opinion shall be made
available for public inspection during such 45-day public comment
period.
PROPOSED FINAL DRAFT OPINION AND ORDER
OF THE BOARD
(by Mr.
Goodman)*
This matter originally
came before the Board on a Petition
for Regulatory Change filed by Amoco Chemicals Corporation on
June
9,
1975.
That proposal, docketed as R75-9,
sought amendment
of Rule
206, Carbon Monoxide, of Chapter
2:
Air Pollution,
of
the Board’s Rules and Regulations.
Ill. PCB Regs.,
Ch.
2,
Rule
206.
The petition~spurpose was to avoid the enforcement of exis-
ting carbon monoxide standards
in
Rule 206(c) (petroleum and petro-
chemical processes)
against emissions
from operations
at the
Amoco Joliet plant.
See,
Amoco Petition,
¶2; R.62.
After the first hearing in the matter,
three additional
parties
(Stepan
Chemical, Koppers
Co.
,
Rn
cIih’lcl
(‘hr’rnical)
also
f
i
mci
U~qula
tory
Pet
it
ions
,
as so
L
or
Lh
ho tow.
‘I’iie common
cause
amonq
the
four
petitioners
is a specific chemical process, also
described below,
and a contention that such processes should not
be regulated under standards applicable to, or designed for, petro-
leum and petrochemical processes.
*The ~
~Tshes
to thank Vincent P.
Flood,
Jr.,
Attorney, Hearing
Officer in this matter,
for his assistance
in the preparation and
drafting of this Opinion and Order.

—2--
THE
PETITIONS
Amoco’s original proposal would have added
a new subsection
(h)
to Rule
206,
specifically governing Amoco’s
~‘Organic Chemical
Partial Oxidation Processes.”
Although AMOCO’s proposed regulatory
change dId not include a definition of “Organic Chemical Partial
Oxidation Processes,” Amoco did submit a proposed definition,
after
the first hearing
in this matter,
to be added to Rule 201 of Chapter
2.
The definition delineated more clearly the areas which Amoco
hoped to encompass
in its original proposal by listing
24 specific,
individual processes,
or groups of processes,
and generally in-
cluding,
“any oxidation process which yields primary products inter-
mediate between
the starting organic material a~:dthe oxides of
carbon.”
Shortly after AMOCO’s proposed definition was received,
the
Stepan Chemical Co. filed a Regulatory Petition of its own
(R76—8),
asking that it be consolidated for hearings with Amoco’s proposal.
The Stepan proposal did not
(like Amoco’s)
ask that a separate
sub-part of Rule 206 be added;
instead, Stepan asked that the
processes
involved be regulated by exception from “petroleum and
petrochemical process”
in a new subsection 206(c) (4)
At approximately the same time, Koppers Co.,
Inc.,
also filed
a Regulatory Proposal,
R76-12,
also asking that
it be consolidated.
Koppers also wished to add a new subsection 206(c) (4).
Shortly after Relchhold filed the fourth Proposal
(R76-l3)
seeking enactment of a new Rule 206(h) (Organic Chemical Partial
Oxidation Processes,
it filed an amendment to that Proposal, with-
drawing the original R76-13,
and asking Board enactment of the
following:
*
“Rule 206(h):
Polybasic Organic Acid Manufacturing Process.
No person shall cause or allow the emission of any gases
containing carbon monoxide into the atmosphere
from any
polybasic organic acid manufacturing process unless the
total fuel value of the waste gas stream is less than 30
of that required for flame incineration of the waste gas
stream at 1460°F,without heat exchange,
and the source
does not cause a violation of the National Ambient Air
Quality Standards,
a source may use approved dispersive
techniques.
Polybasic acid manufacturing processes not
meeting the above conditions shall burn such waste gas
stream in
a direct flame afterburner so that the resulting
*As noted below, p.16,
the proponents generally concurred in
Reichhold’S Amended Proposal after the close of the hearings.
It is therefore the only proposal reproduced fully here.
28-88

—3—
concentration of carbon monoxide
in such waste gas stream
is
less than or equal
to 200 ppm or such waste gas stream
is controlled by other equivalent air pollution control
equipment approved by the Agency accordinq
to the provisions
of Part
1 of this Chapter.”
With
its second proposal,
Reichhold also asked for a new
definition
in Rule
201 to accompany the proposed Rule
206 (h):
“Polybasic Organic Acid Manufacturing Process:
Any process
involving partial oxidation of hydrocarbon with air to manu-
facture polybasic acids or their anhydrides,
such as maleic
anhydride,
phthalic anhydride,
terephthalic
acid, isophtha-
lic acid,
trimelletic anhydride.
A polybasic manufacturing
process
is not a petroleum or petrochemical process.”
A final proposal,
called “unofficial” by the Agency, was
made by Reichhold in its briefs.
Reichhold suggested that the
Board take the option of simply not regulating “partial oxida-
tion processes,”
In either of two ways:
(1)
The Board could
define “Petrochemical Processes”
to exclude the various
petitioners’ processes;
or,
(2)
it could simply declare that
the petitioners’
“partial oxidation processes” are not governed
by Rule 206(c).
THE PROCEEDINGS
The Board originally authorized hearings on the Amoco
proposal,
R75-9,
at its meeting of July 31,
1975;
the proposal
was published
in Environmental Register #107, dated August
5,
1975,
(Ex.
2).
After additional publication,
and public notice
pursuant to the Board’s Procedural Rules,
a hearing was held in
Joliet on the Amoco proposal on February 24,
1976.
That hearing
was concerned almost entirely with the operations and emissions
associated with
the Amoco Joliet plant.
The Stepan proposal was filed on March
22,
1976, and authorized
for hearing and publication on April
8,
1976.
At that hearing,
the
Board also entered an Interim Order allowing Stepan’s Motion for
Consolidation.
R76—8 was published in Environmental Register
#123.
Addtional Interim Orders were entered on May 6,
1976, and June
18,
1976,
granting similar motions by the Koppers Company
(R76—12)
and Reichhold Chemicals
(R76-l3).
Those proposals,
as set out
above, were published in Environmental Registers
#125 and #128,
respectively.
28-89

—4--
Further hearings c~ the merits
of
the
various proposals were
then
held
on
July
12 and
13,
1976,
and March
7,
1977
in
Chicago.
The Hearing Officer also granted
motions
to
include
in
the
record
in this matter the voluminous records generated
in prior adjudica-
tive cases.
ReichholdChemica1sv~ EPA, PCB 73-539,
74-111
(Consolidated);
Stepan Chemical Company v.
EPA, PCB 74-425,
17 PCB
105
(1975).
The records
in those eases were given exhibit Nos.
31
and 32, respectively.
Additional evidence on the m&rits was also
entered, principally by Koppers,
at the second of two Economic
Impact hearings,
held March
21,
1977.
An Economic Impact Study,
as required under P.A.
79-790, was
filed by the Institute for Environmental Quality on December
22,
1976,
(IIEQ Doc.
#76-28;
Ex.
E-l).
Hearings on that study were held March
7 and
21,
1977,
in Chicago and Springfield.
Additional Interim Orders,
related to briefing schedules, were
entered on May
12 and 26,
1977,
There
is still outstanding a Motion,
filed by the Agency on May
5,
1977, asking that final decision
in
this matter be deferred for a period of one year,
to allow the pro-
ponents
to gather
additional
ArnJ~icnt
Air Quality
data.
THE
PROCESSES
The
various
proposals
generally
describe
processes
which
the
proponents
wished
to
regulate
separately.
While
specifics
in
those
proposals
may
have
differed,
the
proposals generally were aimed at
processes
using
catalytic
reactions
to
partially
oxidized
organic
feedstocks,
usually
(but
not
necessarily)
derived
from
petroleum
or
another
petroleum
derivitive
(R.46-50).
Data
acompanying
Amoco’s
proposal,
R75—9,
described
its
pro-
cess
as
follows:
“Amoco’s
primary
Mid—Century
oxidation
process
uses
acetic
acid
solvents
with
a
bromine
promoter
and
cobalt
manganese
catalyst
to
oxidize
xylenes
to
dibasic
acids.
.
.Preheated
acetic
acid,
para-xylene
and
catalysts,
together
with
high-pressure
air
are
charged
to
an
agitated
reactor
operating
at
moderate
tem—
perature
and
pressure,
400°—450°F and
330—400
psig.
The
production
of
isophthalic
acid
(IPA)
and
trimellitic
anhydride
(TMA)
at
separate
units
are
similar
except
for
the
feedstock.
Meta—xylene
and
pseudocumene
are
used
in
place
of
para—xylene.
28-90

—5—
Amoco’s
first witn~. s described the process
as “doing a very
simple replacement,”
(R.20).
When
air
is bubbled through the
agitated liquid reactor,
four hydrogen atoms are stripped from
the para-xylene feedstock,
“hoping
to replace
a1
four of them
with oxygen atoms, while at the same time neither oxidizing any
of the carbons or remaining hydrogens in the molecule.”
(Id.)
Unsuccessful reactions result from shearing the benzene ring or
by succeeding in attaching less than the optimum four oxygens,
and
the by-products must then be removed prior to sale.
The resulting
chemical intermediate
is used in making polyester film and fiber
(R.lS).
See,
Ex.
7.
Amoco’s Joliet plant produces approximately
4
of all U.S.
crude terephthalic acid; Amoco has 25-30
of the national market
if its out—of-state plants are considered,
(R.l3l; See, materials
accompanying Amoco’s petition,
R75—9).
Amoco’s Joliet plant
presently produces 100
of the world’s trimelletic production and
100
of the isophthalic acid market in the United States,
(R.l31—32).
In the latter two cases,
however, other products such as phthalic
anhydride can be substituted directly,
(R.l33; but see,
Ex.
E—l,
pp.
25,
28,
34),
Stepan’s
facility
is,
like
Amoco’s,
located
along the Des
Plaines
River
near
Joliet,
1,2
miles
from
Amoco,
(R.l2).
The opera-
tion of the Stepan plant
(the Milisdale plant) was described in a
previous
Board
opinion
in
PCB
74—425,
supra,
a variance proceeding.
Stepan uses an ortho-xylene feedstock reacted to produce phthalic
anhydride.
17 PCB
105,
106
(1975).
A
solid,
white
crystal
at
room
temperature,
phthalic
anhydride
is
used
as
a
plasticizer
to
make
polyester resins and in the paint industry.
The process involves
passing heated air and vaporized ortho-xylene over a solid catalyst
for
oxidation
to
phthalic
anhydride.
The
impurities
in
the
process
include
phthalic
anhydride,
benzoic
acid
(See,
Ex.
32, record at
9
in PCB 74—425.)
The principal emissions
from the Millsdale plant
are phthalic anhydride and carbon monoxide,
(Id.
at
11), with an
off-gas temperature of 140°F.and 1/2
CO,
(id.
at 13).
Koppers also produces phthalic anhydride,
at a plant in
Stickney,
Illinois,
(R.255,
Ex.
36).
Using
steam,
process
air
is
preheated.
The
ortho-xylene
raw
material
is
injected
into
the
heated
air
stream
and
enters
a
fixed-bed
catalytic
reactor
where
an
exothermic,
partial
oxidation
reaction
takes
place,
(R.260)
Heat is withdrawn from the reaction indirectly via salt baths,
and
used
for
steam
generation.
“The
vapor
phase
continues
to a gas
cooler.
.
.
and on
to the switch condensers where the crude phthalic
anhydride is solidified and removed from the gas stream.
The crude
28-91

phthalic
anuydricI~ is
j4.~4
I
rum the swit
rhensers in
cycles,
sent
on t pre~~~
r~ rhe strippe~
mu, and steer
column, where
it is retntr~.
roce a market~
n~oduct,
reaction
gases
pass from the
~ondenser t
~ raucous
where
they
are scrubbed and tF~
austed.”
(R
The
Sti. kney
facility
uses six reactors, whi
i
~tre
various
iewnstream eqinpment
such
as switch condensers and sr~
.rs.
There
:~r. four emission
sources
(stacks),
(R.262)
The
Reichhold plant is located adjacent to
he illinois River
about
six
miles from Morris
Ill nois, about fi~ aen miles
f.~.om
Joliet,
and forty-seven tc fifty
aix miles from
intown Chicago,
(Ex.
31, Transcripts,
Vol.
2 at
p
6Th,
The Rd
aid plant proluces
maleic
anhydride
using air and bunzene, with a catalyst,
in a
reactor
at
specific temperatures.
The off-gases are cooled prior
to
entry
into
primary
recovery r ~ts
(switch
condensers).
Additional
maleic
anhydride
is
recovered
~n tn~successive
ater and caustic
scrubbers,
the
caustic
scr’ibber
r~erting
any renaming maleic
an
hydride
to
sodium
malate,
wnic.
~hen incinerated.
The
gas
strE-c.r
is
also
passed through
carbor
a
~ers to recoxor unreactec’
er~~e
Reichhold
testified that carbon
xide
is an
navoidable by’produu
of
the
exothermic
reaction ir~’
in
maleic
anhydride
productio~
(id,
at
75—76;
See,
Ex.
32,
B 73—539,
7~.-~li1consolidatedl
Ex~
31
in
this
~~tcr)
It
can be seen that
che~e
tour companies use essentially the
same processes,
with s1i~htvariations,
us.~ng
S
.xlar organic
feedstocks.
There
was
some discussion
as
to whether any
firms
or
chemical
processes
other than the proponents might be co~ered under any of
the
proposals,
(R.667;
Ex,
71)
The
Agency
did supply a list of
those
who
would
potentially be effected
by
a
specific
regulation
for
partial
oxidation processes
That list, however, was compiled
for
the
1964-1966
period.
(see, Public Comment ~12).
The list
indicated
several
producers besides
petitioners
in
this
case
which
might
conceivably
fail
within
the
definitions
offered
by
the
parties
for
partial
oxidation
processes,
rhc
c
included
Witco
Chcmic.il
Company
(Chicago),
the Sherwin~Wi1liams Company
(Chicago)
Ciark
Oil Company
(Chicaqo)
and Gulf Oil
(Calumet City).
Each
of those
additional potentially
effected producers was, according to the
Agency’s list,
engaged
in processes which would have been included
within Amoco’s list of affected processes proposed
as
an appendx
to Rule
201,
(see page
2 supra).
As noted in the record, no~e~rer
(R.667),
that list is probably absolute.
The Institut&s
contractor
found that there are,
at p~’esent, only four chemical firms that use
partial oxidation
processes
in the manufacture of their products:
the
four
proponents here,
(Ex.
E-
1.
at
2,
26,
29—33, Tables 6~9).
211-92

The best evidence before the Board,
then,
is
tTh.
uie
only
four
firms potentially effecred in ml.
matter are ~iase before us here,
We therefore limit our anall~rJ~to
cheir emissions and the effects
of such emissions.
EM~ ~(rTS
Amoco’s emissions are descc.~.cc.
in various places throughout
the record.
The existing units cc
~he Joliet Plant discharge from
7,583 SCFM to 10,833 SCFM per hour
(36,416 to 51,620 lb/hr).
Of
those discharges, nitrogen conscicates from 92—95
of the total.
Carbon monoxide,
on the other hard
ranges from 0.1
to 1.2
(Ex.
9;
see also Ex.
19,
Table I).
Amoco’s permit application for
the Joliet Plant showed a total dincharge of 834 lb/hr of CO,
(Ex.
8).
Agency calculations,
on the other hand,
show a total discharge by
Amoco of 700 lb/hr, or 1,980 tons/yr,
(Agency Brief at
3).
The
exhaust gases from the Amoco Plant are discharged at approximately
100°F, (e.g.
R.98).
Stepan’s process results
~charges
of 192,000 pounds of
air and about 1,000 pounds of
c
monoxide
per
hour, with trace
amounts of organic chemicals
00 lb/hr of carbon dioxide,
(Ex.
32, PCB 74—425,
Record
ci..
The
discharge
is 1/2
CO, at
an exit temperature of 140°F
~t
14).
Agency calculations
indicate Stepan’s discharges
Jah
lb/hr,
or 3,460 tons/yr.
Koppers discharges are somewhat
greater
fo~
all components,
but similar in relative composition
A total
of
4,400 lb/hr of CO
is discharged,
at a concentration
of 3,700 ppm in a waste stream
composed largely of nitrogen
(730,000 ppm),
oxygen
(160,000 ppm)
and water
(65,000-86,000 ppm).
(See,
e.g.,
Ex.
42).
The Agency’s
calculations for Koppers were 3,970 lb/hr of CO,
or 15,670 tons/yr.
Carbon monoxide is also an enavoidable by—product of the
manufacture maleic anhydride
at the Reichhold plants,
(Ex.
31,
Record in PCB 73-539,
74—111, at
75)
.
The off gases from the
maleic manufacturing processes include 1.7
carbon monoxide, 16
oxygen, with the remainder largely nitrogen,
(e.g.
,
id., Volume
II at 101;
see also,
id.
at Ex.
10:
3,360
lb/hr).
The
Agency
esti.mnt(~d
Reichho1d’s~discharges
as
10,000 tons/yr.
In
summary,
although
the CO emissions
vary
from
Petitioner
to
Petitioner,
it can be seen that the makeup of the
Petitioners’
total
emissions
is
quite
similar from
Petitioner
to
Petioner.
The
Agency’s
estimate
of
total
CO
emissions
for
all
four
Petitioners
is
31,050
tons/yr.
28-93

—8—
Ar~iBIENTAIR QUALITY
All four of the Petitioners
in this matter are located
generally near Chicago.
Although there were no 1976 violations
of
the 35 ppm one-hour ambient air quality standard in the
Metropolitan
Chicago Interstate Air Quality Control Region
(No.
67),
there were
violations
of the
9
ppm eight-hour ambient air quality
standards.
Five different sites
in the region
(containing all of the Peti-
tioners)
recorded excursions above
9 ppm; all of those violations
took place within the city of Chicago.
See,
Illinois Environmental
Protection Agency,
1976 Annual Air Quality Report,
at 78,
91.
(We
shall,
for purposes of this analysis,
take notice of the Agency’s
1975 and 1976 Annual Air Quality Reports).
One of those five sites
recording excursions had only one reading in excess of
9 ppm, which
is allowed under the ambient standard, Rule 310(a) (1).
The remain-
ing four sites had,
total, twenty-two instances where the
ambient
air quality was standard,
sixteen of those being concentrated at
the
CAMP Station
in downtown Chicago,
(id.
at 91).
These figures are considerably better than those recorded in
1975.
In that year,
there were both more sites registering viola-
tions,
including Joliet with two excursions above
9 ppm,
and a
greater number of violations
(although most of the decrease resulted
from improved readings at the CAMP and Cermak Stations
in
Chicago).
See,
1975 Annual Air Quality Report at 40,
82, Table 12.
Testimony by Dr. Babcock in 1975,
in the Reichhold
variance
case,
indicated total CO emissions in the region of approximately
3,000,000 tons/yr.
(PCB 73—539,
74—111
(Consolidated)
Vol.
II,
at
23.)
At that time, estimating Reichhold CO emissions of 15,000
tons/yr,
Dr.
Babcock
found
that
Reichhold’s
emissions
constituted
roughly four tenths of 1
of those
in the region.
(id. at 24).
Using
instead
the
Agency’s
estimates
for
all
four
Petitioners
in
this
matter
amounting
to
31,050
tons/yr,
we
see
that
the contri-
bution of all four sources to the total
CO in the region
is approxi-
mately 1
or less.
*
In addition to the general information on carbon monoxide
available for the region containing the Petitioner’s plants, each
of the Petitioners has individually submitted both modeling
and
monitoring results.
Such data was first submitted to the
Board
in the Stepan variance, PCB 74-425, supra.
Although the placement
~Thabco~~tifI~d
that the principal contribution to
ambient
CO is by the automobile, which leads to existing air quality vio-
lations
in areas of heavy auto traffic.
The Agency’s Annual Air
Quality Reports
for 1975 and 1976 agree, stating that,
“the
major
source.. .by far
is the motor vehicle.”
1976 Annual Air Quality
p~~tat 10.
Dr. Babcock estimated that motor vehicles account
for over 2/3 of the total,
in ex.cess of
2 million tons/yr.
73-539,
74-111
(Consolidated),
Record,
Vol.
II
at
23.
28-94

—9—
of
the
monitors
in
the
ritial
study
seems
so~
it
arbitrary,
(PCB
74-425,
Record
at
and
readings
were
t
n
for only
the
month of August,
1974,
(Id. at
59), Stepan’s mo.~oring
contractor
reached the opinion,
“that
J~rn
..
is
no signific
impact
from the
emissions
from
Stepan.”
(id
~
61).
(A1thc~
.
there was one
eight—hour
violation,
at
11
ppm,
Lhe
wind
direc~uon
precluded
any
Stepan contributions;
that excnr’-. ~n was attributed
to
“automotive
exhaust
or
some
other
form.”
(id.
~.t
62).
Most
readings
were
on
the
order
of
2
ppm,
(id.
at
Ex.
11,
12;
but see,
Id.
at
R.67).
Again utilizing Dr.
Babcock, Stepan
presented evidence to show
that
its
emissions (assuming 4500 tons/yr Ca) arount to approximately
0.1
of
the
CO
in
the
air quality control
regic
Dr.
Babcock
testified
that
Stepan’s emissions
would
not
ha’....
any
effect
whatso-
ever on violations
in downtown
Chicago, and would be unlikely
to have
any effect on excessive concentrations elsewhere in the region,
due
to its remoteness from concentrations of automobiles,
(Id.
at 85).
Stepan’s final exhibit
in
that proceeding,
(id.,
Ex.
14), was
a
study showing the general
effect
‘I a change to Rule 206 (c), finding
that the effect on CO
ambient a:r
quality would
be
negligible,
even
if applicable to such major
emi7t’~
n
as refinery.
Reichhold’s ambient air
qi
.
ty
data was also submitted in a
prior adjudicative case,
PCB
73
P39,
74-111
(Consolidated),
supra.
Testimony there indicated
that
.
violation of the ambient air quality
as a result of Reichhold’s
operations
was possible, but only under
extremely adverse
meteorological
conditions, inluding a combination
of low wind speeds,
unstable
conditions and the presence of a very
low level inversion;
even
under such conditions,
violations could
take place only within a radius of 300 meters
from the stack, with
concentrations decreasing rapidly both closer to and farther from
the emission source,
(73-539,
74-111, Record at 10—14; but see,
Id.
at 18,
19).
Using Agency figures and Reichhold modeling,
it was
estimated that Reichhold might contribute 0.4
to the total ambient
CO in the Metropolitan Chicago air quality control region.
Again,
the contribution was termed “negligible.”
(id.
at 25).
Reichhold did not monitor at its plant.
Instead, Reichhold
submitted the results of the study prepared for Commonwealth Edison
at Collins Station, approximately one mile from the Reichhold plant,
(id.
at 117).
Reichhold also noted that a study was made at the
Amoco Joliet plant, about six miles from Peichhold’s facility,
(id.).
Although the monitors in the Edison study were obviously not placed
to record contributions
by
Reichhold,
the use of wind data made
possible some analysis of the effect of its emissions,
(see,
id.
at
122).
Although the monitoring period was short
(again, one month),
the results of the study do show that CO
is not generally a problem
in the vicinity of the Reichhold plant,
(id.
at 126).
28-95

—10—
Amoco’s modeling
an.
xonitoring results were submitted at
the
first hearing
in this matter.
The highest one-hour value for
CO
recorded
was
5.9 ppm;
the
highest
eight-hour value was
4.28
ppm,
(R.88).
The data gathered
during
Amoco’s monitoring program
correlated generally with dispersion modeling, which did not
indi-
cate potential violations,
(R.92;
Ex.
15).
Like the monitoring
studies undertaken by Stepan and Reichhold, however,
the Amoco
program was conducted for a limited time:
March and April,
1974,
(R.84).
Additional
information
was
submitted
by Amoco at the July
12,
1976
hearing,
(see,
e.g.,
P.213, Ex.
34).
Again, a violation
was
not
indicated.
Koppers
is
located
closer
to
those
downtown
Chicago
areas which
have
experienced
ambient air quality violations
for CO, although
its
Stickney plant is still considerably removed
from any of the
monitors
which have indicated violations.
As with the other companies,
Koppers presented testimony and evidence that would support its con-
tention that its CO emissions could
not either have caused
violations
in the neighborhood of its own
plant,
or have contributed to
the
existing violations farther away.
Although there were some
anomalies
in the test results,
(e.g.
R.509-531), and the monitoring
loc~tions
may not have been perfectly
chosen.,
(P.405), Koppers’ modeling
generally showed that its emissions
did not cause CO ambient
air
quality
violations,
(e.g.,
P.436).
Finally,
some additional data with
regard to the Stepan monitor-
ing, corroborative of the data received in PCB 74-425, was introduced
by Stepan for cross-examination purposes,
(P.534).
CONTROL
TECHNIQUES
It
was
the
general contention of all of
the
Petitioners
in this
matter that the carbon monoxide emissions from their plants,
as
detailed above, simply cannot be controlled to the levels required
by
Rule
206(c)
in
an
economically
reasonable
manner.
Most
of
the
testimony and evidence presented by the parties
in this matter,
as
well
as
the
preponderance
of
that
seen
in
the
earlier
adjudicative
cases, concerned the costs and technical difficulties associated
with
the
control
of
CO
emissions
from
partial
oxidation
processes.
The
Board
has
been aware of these
issues for some time;
as the
Agency points
out, the
issues
here
have been presented more or less
continuously since
1973.
See, e.g.,
PCB 73—365,
PCB 74—63,
PCB 74—325, PCB
75—350
(Koppers);
PCB
73—539,
74-~ll1 (Consolidated),
supra
(Reichhold); PCB 73—460,
74—425,
76—161
(Stepan).
The proponents concentrated on four methods for the removal
of
carbon monoxide from their emissions.
28-96

—11—
(1)
Incineration;
at
approximately
1500°F.,
.‘arbon
i~Td~Ts
effectively oxidized and eIu~d.nated.
This
method,
for
these
Petitioners,
recuires
considerable
fuel
input
inasmuch
as
th~
if-gases
are at a
very
low
temperature
with
lit.le
fuel value,
(as described above for
each
Petitioner).
(2)
Incineration with heat recovery
under
this
method,
both
conventional
and
innovative
heat
recovery
techniques are employed to
cut
fuel
requirements.
(3)
Cold
catalytic
oxidation
the
Board
discussed
this
method
previously
in
variance
matters,
supra,
while
research
was
being funded,
The
~rograms
have
been
dropped
because
-—
despite
some
laboratory
successes
--
the
method
has
not
proven
feasible.
(4)
Thermal catalytic oxidation
this method, while not
~
fuel necessary for
incineration, does require some energy input
for successful
CO removal.
This method, dis-
cussed chiefly in terms
of a Du Pont proprie-
tary system,
is also useful for removing
other contaminants such as hydrocarbons.
It
was covered extensively by the par’ties and
in cross-examination by the Agency.
There was
even
some
discussion
of
recovering
heat
from
the exothermic partial oxidation process
itself in conjunction with this method.
The parties also discussed briefly the additional possibility
of using exhaust gases from the partial oxidation processes
as
combustion air for other requirements
at the Petitioners’
facili-
ties,
such as steam boilers.
Because of the quantity of exhaust
gases involved, however,
this method was shown
to be impractical.
Incineration.
There can be no question of the fact that incine-
ration does constitute a technically practical method for the
eliminaH~3’~iof carbon monoxide from the Petitioners waste gas streams.
Although the parties presented arguably
valid evidence to the effect
that combustion by-products of incineration
(e.g.,
SO2) would con-
stitute worse pollution
problems than uncontrolled
Ca,
and to show
the unavailability of fuel for such incineration, their principal
contention with regard to incineration as well as the other
potential control technologies was one of simple cost-benefit.
28-97

They
argue
that the reJ’
..~
small
amounts
of
i
removed
canno~
justify
the
enormous ca~ ta
and
operating
costs
involved.
In its most recent
varinn~
u~se,
PCB
76-li
,
Stepan
estimated
that
the
incineraton
of its em~scons would
require,
in
addition
to
any capital costs,
4,000,000 ga1lo~is
of
fuel
oil
per
year,
(PCB 76~
161, Record
at 23).
That figure
quite compatible with the
evidence
received
in
this matter.
hoppers,
for example, estimated
that
even
with
heat
exchange at a maximum
of 57,
961 gallons
of
fuel would be required
each hour,
or a
total
of 7,611,000
gallons
per year,
(Ex.
50).
Amoco
estimated
that
incineration
would
require
2,000,000 gallons
per year of No,
6 fuel oil,
(Fx,
20).
As
early as
1971,
Reichhold had
estimated that its
1.7
car~
on
monoxide
waste
gas would require
.075 MBTU’s for every
1,000
lbs.
of exhaust
gas to
achieve incineration,
or 45,000,000 BTU5 per hour.
Even if natural
gas
were
available
at
that time
(1971),
the necessary natural
gas
would have cost
$250-300,000
per
year,
with
a
capital
cost
for
the
incinerator
of
$300,000-400,000,
(PCB
73—539,
74—111
(Consolidated)
Ex.
36,
at
2),
Gas is now unav~..
able for such purposes,
of course,
and prices
for
fuel
and construction
have
risen.
Heat
Recovery.
In add~t.~.o~o
normal
heat
recovery
systems.
Koppe~T~stigateda
“Reeco”
..em
utilizing
extremely
high
heat
exchange
(85-90).
The un
s Involved would cost
$5,000,000,
with
operating
costs in the banl~of
$400,000—600,000
per
year,
(P. 314).
Such
units
have
not been
widely tested.
Cold
Catalytic
Oxidation.
hoppers
also
investigated
various
—~-.—
—,--—_,~..-—-—-.
cold catalytic oxidatron control systems,
going
so
far
as
to
solicit bids from
vendors,
(P.280-301).
Pilot
plants
were
actually
installed,
(Ex.
53).
In general,
due to catalyst blinding,
systems
upsets and unsatisfactory emissions,
the systems have been very
unsatisfactory.
Thermal Catalytic Oxidation.
Stepan has done considerable
work with the Du Pont Catalytic Reactor System.
This system
opercte~
by heating the off gases
and passing
them over a catalyst; hydro-
carbons are oxidized
to carbon dioxide
and
water
while
carbon
monoxide
is oxidized to
carbon
dioxide.
In addition, it
appears
that
heat
exchange
may
significantly
reduce the need for
supplementa.~
fuel for the system’s
operation.
In
its
most
recent
variance
reques~
Stepan
proposed
the
installation
of
such a unit, for the
control
of
hydrocarbon emissions as well as carbon
monoxide; reductions
in plant
discharges have been estimated at 85—95
for organics and
96-100
for
carbon monoxide in
pilot
plant
testing.
28-98

—13—
Whether the Du Pont system would be applicable to the other pro-
ponents, however,
is unclear.
Amoco, Rappers,
and Reichhold utilize
other methods for hydrocarbon control,
increasing the relative cost
of such
a system for
CO control.
Again,
in
summary,
control
of CO emissions
from partial oxi-
dation processes is technically practical.
Given sufficient fuel
for incineration, or sufficient capital investment for catalytic
reaction, each
of the Petitioners could readily comply with the
200 ppm CO standard in Rule 206(c).
The issue,
simply,
is cost.
ECONOMIC
IMPACT
The Institute’s Economic Impact Study,
IIEQ Document No.
76-28,
concludes that,
“although thermal incineration
is technically and
economically feasible.
.
.
this method would be inefficient because
incremental social benefits appear to be significantly less than
incremental social costs.
Even though the social costs of thermal
catalytic oxidation would be
less,
we still conclude that compliance
with Rule 206(c)
is inefficient using the least-cost method, since
these
firms contend that they meet Federal standards for CO emis-
sions.
“In the long run,
if all four firms complied with Rule 206(c),
the loss of social benefits from plant relocations and the impact on
energy would make compliance with Rule 206(c)
inefficient.”
(Ex. E-l
at xvi).
Section 6(b)
Coverage.
Sec.
6(b) of the Act requires that the
institute’s studies consider a wide range of specific environmental
and economic effects which might be associated with proposed regu-
lations,
as well as contain,
“an evaluation of the environmental
costs,
and benefits of the rules and regulations
to
the People of
the State of Illinois,
including the health, welfare and social
costs and benefits.”
Ill.Rev.Stat.,Ch.lll
1/2,
§l006(b)(l)
(1977).
The study in this matter considered all of the various sectors set
forth there, under the same short—run/long—run basis noted
in the
conclusion quoted above.
See,
e.g.
Ex.
E-l at Table
1,
ch.
V.
The
study’s investigation of economTc effects, based on comparisons
between enforcement of the present regulation and the effective de-
regulation proposed by the parties, was adequate and generally
supportive of those quoted conclusions.
The macro-economic effects described in the study
(indicating
excessive cost and little benefit resulting from enforcement of Rule
206(c)
as
it exist)
result principally from macro—economic effects
upon the four firms constituting the organic chemical partial oxi-
dation industry in
Illinois.
The study found that although
--
in
28-99

—14—
the short
term
--
enfo.~.c~mentof
Rule
206(c)
would
impact negatively
only
upon
the
four
prod~
rs,
short and long terms eUects
upon
those producers would negatively impact the economy
of
Illinois
generally.
As
“price takers”,
with
fragile market
shares,
Illinois
producers are unable to raise prices by amounts
neces~ary
to offset
the costs which would be associated with Rule 206(c)
compliance.
See,
e.g.,
Ex.
E-l
at
32.
As
a
result,
the
study
found
that
Illinois
producers
would,
in
the
indeterminate
“long
run”,
be
forced
to
relocate elsewhere, with significant, general, negative impact for
Illinois.
The study performed in-depth analysis of the cost of compliance
upon each of the companies.
Although there were
some
corrections
of
the figures used by the
Institute
at the hearings,
the data nonethe-
less
indicated
that
the
enforcement
of
Rule
206(c)
limitations
for
CO against the four firms would result in cost
increases
which
could
not be offset by price increases,
(id.,
Ch.
IV,
§SB—D),
The only significant dispute regarding the economic study was
the
Agency’s
contentions
that,
(1)
the
study
was
in
error
when
it
found
that
the
benefits
of
enforcement
could
not
be
properly
computed,
(e.g., Ex. E-l at 69-~74); (2)
the
study was
in error when it assumed,
for benefit measurement,
that none
of the four impacted firms
would
cause or contribute to a violation of ambient air quality standards,
based on a lack of
adequate
data,
We
find
that
these
issues
are
properly resolved using,
for benefit analysis,
our ambient air quality
standards for carbon monoxide; we shall discuss below the adequacy of
the data before us.
ISSUES
Although the adequacy of the record on the question of ambient
air quality compliance
is unquestionably the major issue which we
must decide,
there ar~
several issues which the parties raised
throughout this proceeding.
(1)
In both the prior Stepan and Reichhold
variances as well as this regulatory pro-
ceedirig,
the parties argued at length that
it
was
never
the
Board’s
intention
that~
organic
chemical
partial
oxidation
processes
be regulated by Rule
206(c).
(2)
Are the Petitioners’ processes “petroleum or
petrochemical” processes?
The parties argued
that regardless
of what might have been the
Board’s
original
intent,
their
processes
are
not
petroleum
or petrochemical processes,
and
should not be subject to the same standards
as,
e.g.,
refineries.
28-100

15—
(3)
Is it tech ~ica1ly practicable for
the
Petitioners,
or their ~,ocesses, to meet the 200 ppm standard
of Rule 206(c)?
.1~1though, as we noted above,
thermal incineration is an effective control
method for carbon monoxide, there are nonethe-
less problems with enforcing the regulation.
Principally, the parties argued that it
is
irrational to apply a “50
excess air” criteria
to their processes,
inasmuch
as excess air limi-
tations are generally used to prevent the dilution
of waste gas streams.
The parties discussed this
question at length in the prior variance hearings,
and at the hearings on these regulatory proposals,
(e.g.
R.36—40).
(4)
Is
it economically reasonable to require that the
proponents here comply with any carbon monoxide
standard?
Since we decide that the ambient air quality data is adequate,
and does support proponents’
position, and that the enforcement of
Rule 206(c)
or some other standard against the proponents would be
economically unreasonable, we specifically decline to answer any of
the other issues raised.
Whether the Petitioners’
processes were considered by the Board
in the enactment of Rule 206, or whether they are “petrochemical”
processes,
is immaterial,
inasmuch
as we choose to regulate these
processes
separately.
We need not discuss the application of “50
excess air”
to the Petitioners emissions,
or the availability of new
control techniques such as Du Pont’s,
since
the ambient air quality
and cost data before us
justify the separate regulation of Peti-
tioners.
The Agency contested
-—
rather strenuously
——
the adequacy of
the modeling and monitoring performed by the proponents
to show that
a regulatory amendment would not cause ambient air quality problems.
Although there were some
quest~ons
r~S
to monitor placement in some
of the monitorinq situations,
(see
supra),
the Aqency did not
seriously
question
the
quality
of
the
Petitioners’
modeling
or
monitoring; extensive cross—examination did not uncover any serious
flaw
in
the
proponents’
methodology
or
performance.
Rather,
the
Agency
attacked
the
sufficiency
of
the
proponents’
presentations
in
quantity
terms.
The
Agency alleged that the Petitioners models were
not
calibrated,
or
did
not
include
all
meteorological
conditions;
monitoring,
the Agency claimed,
likewise did not cover all expected
weather conditions.
28-1 01

—16--
The essence of the Agency’s
argument, and
it.s pending motion
noted above,
is that more information, predictive and historical,
is needed before the Board can make an informed judgment on the
effect the proposed regulatory change(s).
Further narrowing its
argument,
the Agency has not really questioned the effect of the
proposed regulatory changes upon ambient air quality with regard to
operations by three of the Petitioners:
Amoco, Stepan and Reichhold.
They are located away from Cook County in areas with few other CO
sources, where there are not ambient air quality violations;
the
sources
in question will probably not cause or contribute to viola-
tions of the one-hour or eight-hour standards.
We agree with the
Agency,
however,
that closer analysis
is needed with regard to
Koppers’
emissions.
As noted above, Koppers is located in a suburb adjacent to
Chicago,
in an area where
it might conceivably contribute to an
ambient air quality violation.
(Essentially all
Illinois
ambient
air quality violations for CO are located in Chicago.)
However,
as we also noted above, Koppers
is
located away from problem areas
within Chicago.
Although it is located near some potential areas
(two race track parking lots and the Stevenson Expressway),
hoppers
modeling and monitoring
-
albeit imperfect
indicate that it will
not contribute
to a violation.
All the proponents’
data on ambient air quality, predictive
and
actual,
is certainly imperfect.
In places,
it is far less than
perfect.
It is sufficient,
however,
to show that the proponents’
CO emissions are highly unlikely to cause or significantly contri-
bute to any ambient violation.
There is even a possibility that
control technologies would contribute to violations of other
standards,
e.g.,
SO2.
Weighing that likelihood against the economic
effects, micro- and macro-, separate regulatory treatment for the
proponents has been justified.
We shall therefore deny the Agency’s
motion to require additional data and defer action,
and shall instead
enact the regulatory change requested.
There remain, then,
two final issues for decision:
(1) which
of the various proposals should be adopted, with what changes; and
(2)
should any proposal be applied prospectively
to
plant expansions
or new plants?
By the conclusion of the hearings in this matter,
the proponents had generally settled upon Reichhold’s amended petition,
supra, as a consensus position.
We agree, because that proposal
limits
—-
in both the proposed Rule 206(h)
and the accompanying defi-
nition
——
the coverage of the change.
We shall amend the proposed
Rule 206(h),
however, by deleting the references to ambient air
quality,
finding that proposed provision duplicative of existing Rule
102
(prohibition of air pollution).
We shall also amend the proposed
definition insofar as it defines
In the negative with regard to
28-1 02

-
17-
petroleum or petrochemical
processes;
since we
are
separately regu-
lating the processes in
question, it
is immaterial whether they are
or are not petroleum or
petrochemical
processes.
With regard to coverage,
we feel
that no specific limitations
are necessary.
Some of the
Petitioners plants have been recently
expanded, apparently without
adversely
effecting ambient air quality;
Rules
102 and 303 will provide adequate protection with regard to new
partial oxidation processes.
Finally, we note
that the Agency
questions
its ability to
obtain U.S. Environmental Protection Agency approval of a State
Implementation Plan
(SIP)
amendment based on the existing ambient
air quality data for partial oxidation processes and carbon monoxide.
We feel that,
in light of the relatively minor CO emissions involved
(as compared to total area CO emissions, principally motor vehicle
related),
the fact that other
states
do not regulate the emissions
in question, and the area’s
trend
towards compliance,
such approval
should be obtainable.
The Board therefore adopts
as its Proposed Final Draft Order
in this matter the following.
PROPOSED
FINAL
DRAFT ORDER
It is the Order of the Pollution Control Board that Rule 201,
(definitions)
of Chapter 2:
Air Pollution of this Board’s Rules
and Regulations be amended by addition of the following new defini-
tion:
Po~~sic9~~4c Acid Partial Oxidation Manufacturing Processes:
Any process involving partial oxidation of hydrocarbons with
air to manufacture polybasic acids or their anhydrides,
such
as maleic anhydride,
phthalic anhydride,
terephthalic acid,
isophthalic acid,
trimelletic anhydride.
Rule
206, carbon monoxide emissions standards and limitations, of
Chapter
2:
Air Pollution of this Board’s Rules and Regulations
shall be amended by addition of the following sub-section
(h):
(h) Po~
.sicOrq
idManufactur4~r22e!~~. No
person shall cause or allow the emission of any
gases containing carbon monoxide into the atmosphere
from any polybasic organic acid manufacturing process
unless the total fuel value of the waste gas stream is
less than 30
of that required for flame incineration
of the waste gas stream at 1,460°F,without heat
exchange.
Polybasic acid manufacturing processes not
28-103

—18—
meeting the abov:~conditions shall
burn
uch
waste
gas
stream in a direct flame afterburner to achieve
a
resulting concentration
of
carbon monoxide
in
such
waste gas stream of less than or equal
cc 200 ppm, or
shall employ such other,
equivalent control method
or equipment as may be approved by the Agency according
to the provisions of Part
I of this Chapter.
Mr. Werner dissents.
I,
Christan
L.
Noffett,
Clerk of the Illinois Pollution Control
Board, hereby certify the above Proposed Final t~ra~t
Opinion and
Order were adoi~ted
on Lhe_~’’
day of ~
,
1977
by a vote of
‘/-
I
Illinois Pollutio’
Board
28-1 04

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