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