BEFORE
THE ILLINOIS
POLLUTION
CONTROL
BOARD
IN THE
MATTER
OF:
PROPOSED
AMENDMENTS
TO
TIERED
APPROACH
TO
CORRECT
WE
ACTION
OBJECTIVES
(35 111.
Adni
Code
742)
Dorothy
Gunn,
Clerk
Illinois
Pollution
Control Board
James
R.
Thompson
Center
100 W.
Randolph,
Suite 11-500
Chicago, illinois
60601
(Via First
Class Mail)
Matt
Dunn
Environmental
Bureau
Chief
Office
of the
Attorney
General
James R.
Thompson
Center
100
W. Randolph,
12
th
Floor
Chicago,
Illinois
60601
(Via
First
Class Mall)
Participants
on
the
Service
List
(Via First
Class
Mail)
NOV
142008
POIjtj
STATE
OPHJJNO,S
Control
8oaj
Bill
Richardson
Chief
Legal Counsel
Illinois
Dept.
of
Natural
Resources
One
Natural
Resources
Way
Springfield,
Illinois 62702-1271
(Via
First
Class Mail)
Richard
McGill
Hearing
Officer
Illinois
Pollution
Control
Board
James
R.
Thompson
Center
100W.
Randolph,
Suite
11-500
Chicago,
illinois
60601
PLEASE
TAKE
NOTICE
that
I
have
today
filed
with
the
Office of
the
Clerk
of
the
illinois
Pollution
Control
Board the
Illinois Environmental
Protection
Agency’s
(“illinois
EPA”)
Errata Sheet
Number
I and
the Pre-filed
Testimony
of
Gary
King.
Thomas
C.
HornshawTracey
Hurley.
and
Atul
Saihotra
a copy of
each of
which
is
herewith
served upon
you.
ILLINOIS
ENVIRONMENTAL
PROTECTION
AGENCY
BJ4425
)
)
)
)
)
)
)
R09-9
(Rulemaking-Land)
1ER
OFFICE
NOTiCE
1
&imberly
i/ Geving
Assistant
Ctounsel
Division
of
Legal Counsel
NOV14
21108
STATE
OFIWNOIS
)
R09-9
POll
LJtjOn
Cotoj
Board
)
(Rulemaking-Land)
)
CLER!CS
OFFICE
NOV
142008
STATE
OF
ILLINOIS
ERRATA
SHEET
NUMBER
1
Pollution
Control
Board
NOW
COMES
the illinois
Environmental
Protection
Agency
(“illinois
EPA”)
through
one of
its altorneys,
Kimberly
Geving,
and
submits
this
ERRATA SHEET
NUMBER
I
to
the
Illinois Pollution
Control
Board
(Boardn)
and
the
participants
listed
on the
Service
List.
Gary
King,
TraceyHurley,
and
Thomas
C. Homshaw
will
provide
testimony
in
support
of
these changes
at the
hearing
on January
27,
2009.
Section
741410(b)
AGE
•
of
the
fol14
1
””’
approaches:
1)
—Prescriptive
Apptoaoh:
A)
If
more
thai 15%
of
thc-goundwater-oumpling
rosultci
for-a
ehemical
obained
in aocor.daBe,e
with
subseetion
(a) of
this
Section
are less-than
the
appropriate
detectiei-limit
for
that
itn1
the
Preserij>tive
Approach
may not
heneeti
fur
riiiCfti.
If4-54
or less
of-the
sampling
reau4ts sre
.nii-uu
appropriate
detection
limit,
a
conaenatipn
‘-iJ-uuv
half tha
detection
limit
shall
be uped-i
fhnt
ea4 -in the
cnlc&nlipns
contaffied-in
this
Preseriptive
B)
munctwatep-eemnhinf
re
tf-f)htrn
ned in -wôruicmee
BEFORE
THE
ILLINOIS
POLLUTION
CONTROL
BOARD
IN
THE
MATTER
OF
PROPOSED
AMENDMENTS
TO
TIERED
APPROACH
TO
CORRECTIVE
ACTION
OBJECTIVES
(35
III.
Adm.
Code
742)
.ground
shall
be-determined
accoram
6
—
that
ohc
lestl
ehew
—
Approach.
The-
with
subsection
(a.) of
this
Seotion
shall be used-to
determine-
if-tho
sample
et is nennally
distributed
The
Shapiro Wilk
Test of
Normalityehall-bc
usetho-dotermine
whether-the
sample-act
is normally-distributed,
if the
sample
-set for
the
brick-ground
well(s)
contains
50
or
fewer
1
sampleoValue
aecessay
for the
Shapiro
Wilk
Teo-ef
Normality Ghall
be
determined
ualng
Appendix
A,
Tab
let
C
end-fl.
If
the
computed-value
of
W
is-greater-than
thci4%
Crionl—Vulue
in-Appendix
A,-Table
D,
the sample
set
shaM
be-assumed
to-be-nonnally
distributed,
and
the
Prescriptive
Approach
is
al4wed.
If
the
computed
value
of W is less
then
5<3<,
Ctiea1-Value
in
Appendix
A,
Table
1), the
sample
set
shall
be aaumed
to
not
be
normally disthbutetl-and
the
Pfescriptive-Approach
shall
notl,e used.
C)
If
the
saniple-set-contains
at
least-ten-
sample
results,
the
Upper
Tolerance-Limit
(UTL)
of
a-normally
distiibuted
sample
set
may
be-eulculatod
using the-rn
ccxi
(x)
and
standard
deviation(&)
from:
UTL—
x
+
(K
Whore
K
—the-one
sided neirnal
tolerance
fao4er
for
esating
the
95<3<.-upper
confidence-limit
af-the
95<
percentile
of-a
nomial
distnbution.
Values for
K-shall
be
determined
ming-Appendix
A,
Tablo.
D)
If tho-semple
set
contains-at
least
ten sample
reu1ts,
the
UTL
shall-be-the
upper
limit
of the area
background
cone
ntratien
fer the-
site. If
the-
sample-set
centains-fewor
than
ten
sample
results,
the-maximum
value-of
the sample-set
shall
be
the
upper
limit
of-the-area
backaround
concentration
for
the-site
nr-aqh-shafl
not
be
used
for-dcterminin-a
area
oucicgrounu
icr
me
parameter
nT-i
(b)
Area
background
shall
be determined
by
using
a
statistically
valid
approach
appropriate
for
the
characteristics
of the
data set
that is
approved
by
the
Agency.
742.1210(c)(4)
Remove this
subsection
from
the
proposai.
Appendix
A
Table
A
For
the
chemical 2-Chiorophenol
(ionizable
organic)
change
l.OOE+05
to 1 .OOE+04
and
change
7.OOE+04
to
7JOE+03.
For
the chemical
Dichiorofluoromethane
change
the
spelling
to Dichiorodifluoromethane
and
change
the
820E+04 to
S.70E+02.
For
the
chemical
Mercury
(elemental)
in
the
Soil
Component
of
the Groundwater
ingestion Exposure
Route
column
change the
3.1 OE+OO
to
.
2
For the chemical
Vinyl
acetate
change
the
2.26E+03
to
2QB+O3.
Appendix
A,
Table F
Under
the
category of
the
Respiratory
System
add
l3-Dichloropropene
(cis
+
trani)finhalation
only)
just before p-Dioxane
(inhalation
only).
Appendix
A,
Table
L
For the chemical
2-Chlorophenol
(ionizable
organic)
change
4.90E+04
to
4.90E+03.
For the
chemical
Mercury
(elemental)
change
4.50E-0l
to l.05E+00.
Appendix
B, Table
A
For
the
chemical 2-Butanone
(MEK)
change
the
Outdoor Inhalation
value
from
13,0001)
to
250
d
For the chemical 2-Chiorophenol
change
the
Outdoor
Inhalation
value
from
100
,
000
d
to
10000
d
For
the chemical
I
,4-Dichlorobenzene
(p
Dichlorobenzene)
change
the
Thgestion
value
from
l20eto.QQ.
For
the chemical
1,3-Dichloropropene
(1,3-
Dichioropropylene,
cis
+
trais)
change
the
Class
I
value from
0.003c
to
0.0052e
and
change the
Class
XI
value
from 0.015
to
0.026.
For
the chemical
Methoxychior
change
the
Class
I
value
from
l
4
to
4.
and
change
the
Class
II
value
from
14
dt
0
For the chemical
2,4-Dichiorophenol
change
the
Class
II
value
from
3.3k
to
i2.
For
the
chemical 2,4,6
Trichlorophenol
change
the
Outdoor Inhalation
value
from
430e
to
For
the chemical
Cobalt
change the
Ingestion
value
from
0
600
bt
l,
and change the
Outdoor
Inhalation value
from
1,1
OOe
to
360e
Appendix
B, Table
B
For the
chemical
&omoform
change
the
footnote
under the
Construction Worker
Ingestion
column
from an “e”
to a “b”.
3
For
the
chemical
2-Butanone
(MEK)
change
the
IndustrIal/Commercial
Outdoor
Inhalation
value
from
21,000”
to
25
000
d
and change
the
Construction
Worker
Outdoor
Inhalation
value
from
140”
to
730
b
For the
chemical
Chloroform
change
the
Construction
Worker
Ingestion
value
from
2
,
000
btO
4.000c.
For
the
chemical
2-Chlorophenol
change
the
Industrial/Commercial
Outdoor
Inhalation
value
from
1001000
d
to
10
,
000
d,
change
the
Construction
Worker
Ingestion
value
from
10,000”
to
1600
b,
and
change
the
Construction
Worker
Outdoor
Inhalation
value
from
100000
d
to
For the
chemical
Dalapon
change
the
Construction
Worker
Outdoor
Inhalation
value from
120,00&
i
i,ooo.
For
the
chemical
DL)D
change
the
Construction
Worker
Outdoor
Ingestion
value
from
3()e
to
For
the
chemical
1 ,2-Dibromo-3-chloropropane
change
the
Construction
Worker
Outdoor
Inhalation
footnote
from
“b” to
“e”,
For
the
chemical
Di-n-butyl
phthalate
change
the
Class
I
value
from
1,100’
to
880
d
and
change
the
Class
11
value
from
5,600T
to
For the
chemical
1.,4-Dichlorobenzene
(p
Dichlorobenzene) change
the
IndustriailCommercial
Ingestion
value
from
1,100’
to 140,000”,
change
the
Industrial/Commercial
Outdoor
Inhalation
value
from
6.2c
to
20000
b
and
change
the
Construction
Worker
Outdoor
Inhalation
value
from
8.8 to
3201.
For
the
chemical
1
,3-Dichloropropene
(1,3-
Dichioropropylene,
cis
+
trans) change
the
Class
I
value from
0.003c
to 0.0052
and
change
the
Class
fl
value
from
0.015
to 0.026.
4
For
the chemical
24-Dimethy1phenol change
the
Construction Worker
Ingestion value from
4
l,OOO
to
100b
For the chemical 2,6-Dinitrotoluene
change
the
Class
U
value
from o.OoO
to
ooolgr.
For
the chemical
Di-n-octyl phthalate change
the
Industrial/Commercial
Ingestion footnote
from
a
“d
to
a
“b”.
For
the
chemical
Hexachiorocyclopentadiene
change
the Class II value
from 1
30
d
to
For
the
chemical
Isopropylbenzene (Cumene)
change
the Construction
Worker Ingestion
value
from
82,
00b
to
820
jb
For the chemical Methoxychior
change the
Class
I
value from
14d
to
4
and change the
Class
IT
value
from
14d
to
For
the chemical
2-Methyiphenol (o-Cresol)
add
a
footnote ‘a” after the value
in
the
Construction
Worker
Outdoor
Inhalation column.
For
the chemical
N-Nitrosodiphenylamine
change
the footnote
“e” to
“b” in
the
Construction
Worker
Ingestion column.
For
the
chemical N-Nitrosodi-n-propylamine
change
the
Industrial/Commercial
Outdoor
Inhalation
value from
to O22
and
change
the
Construction
Worker
Outdoor Inhalation
value
from
1,
900d
to
O.31e.
For
the
chemical 2,4,5-TP
(Silvex)
change
the
Construction
Worker Ingestion value from
l6O,OOOl
to
L600b.
For
the chemical
2,4-Dichlorophenol
change the
Class II
value
from
3,3’
to
For the
chemical
2,4,5-Trichiorophenol
change the
Construction Worker
Ingestion value
from 2OO,OOO’
to
5
For
the
chemical
2,4,6-Trichiorophenol
change
the
IndustriallComniercial
Outdoor
Thhalation
value
from
820t
to
630e,
change
the Construction
Worker
Ingestion
value
from
11
,oooc
to
2000
b
and
change
the
Construction
Worker Outdoor
Inhalation
value
from
l,200c
to
89CC
For the
chemical
Antimony
change
the
Construction
Worker
Ingestion
value
from
41
b
to
For
the
chemical
Chromium,
ion,
hexavalent
change
the footnote
in
the
Construction
Worker
Outdoor
Inhalation column
fxm
a
4‘
b”
to an
“e”.
For
the
chemical
Cobalt
change
the
lndustriallCommercial
Ingestion
value
from
4l,000’
to
change
the Industrial/Commercial
Outdoor
Inhalation
value
from
I,Sooe
to
and
change
the
Construction
Worker
Ingestion
value
from
12
,
000
b
to
610
b,
Add
a new footnote
“aa” at the
end
of
the
footnotes
to read:
Calculated
values
correspond
to
soil
concentrations
that should
not
result
in
air
concentrations
that
exceed
criteria
for
workplace
alL
Appendix
B,
Table
G
For
the
chemical
2-Butanone
(MEK)
change the
Soil
Gas
Residential
value
from
440,000
to
380
O0O
and
change
the
Soil Gas
Industrial/Commercial
value
from
2,700,000
to
380.000g.
For
the chemical
2-Chiorophenol
change
the
Soil
Residential
value
from
49,000c
to
4,90Cc,
change
the Soil
lndustriallCornrnercial
value
from
49,00Cc
to
4,900c,
change
the
Groundwater
Residential
value
from
220
,
000
h
to
22
,
000
h,
and
change the
Groundwater
Industhal/Commercial
value
from
220,000
to
22000
h
For
the
chemical
1,4-Dichlorobenzene
change
the
Soil Residential
value
from
I
.3
to 130,
change the
Soil JndustriallCommercial
value
from
98
d
to
J1QY
change the
Groundwater
Residential
value
from
6
085d
to
19,
change the Groundwater
Industrial/Commercial value
from 6’ to
change
the Soil
Gas Residential
value
from
317d
to
84
g
and change
the Soil Gas Industrial/Commercial
value
from
27
OdtO
g,
400g
For the
chemical Mercury
change
the
Soil
Residential value from
O45
to
I
O5
and
change
the
Soil
IndustriallCon-imercial value
from O.45
to
l.
05
c,i.
Change
footnote
“i”
by deleting
“Mercury is
measured in mg/L.”
and
replace it
with
“Value for
the
inhalation
exposure
route is
based on
Reference
Concentration
for elemental
mercury
(CAS No.
7439-97-6).
Inhalation remedialion
objectives
only
apply at
sites where elemental mercury
is a
contaminant of concern.”
Appendix C,
Table E
For the chemical
2-Chlorophenol change the
Solubility
in
Water entry
from
2.20E+05 to
22EO4,
For
the chemical 2,4,5-Trichiorophenol
change
the
Solubility in Water
entry
from
8.OOE+02
to
1 2OE+O3
and change the
Dimensionless
Henry’s
Law Constant (H’)(25°) entry from
3.53E-04 to
1
.78E-04.
For
the
chemical
2,4,6-Trichlorophenol
change the
Solubility
in Water entry from I .2O+O3
to
8OOE+O2 and
change
the
Dimensionless
Henry’s
Law Constant (H’)(25°) entry
from
L78E-04
to
153E-04.
Appendix
C,
Table
3
fri the
pH header
row
change
Hg
to
Hg(+2
for
the
entire
table.
7
DATE: November 12, 2008
1021 North Grand Ave. East
P.O.
Box 19276
Sprirtg±ield, Illinois 62794-9276
(217)
782-5544
8
Respectfully submitted,
ILLINOIS
ENVIRONMENTAL
PROTECTION AGENCY
By:
Assistant
berlyA.G
Counsel
ng
(J
Division
of
Legal
Counsel
ILLINOIS
POLLUTION
CONTROL
BOARD
IN
THE
MATTER
OF:
)
NOV
142008
PROPOSED
AMENDMENTS
TO
)
R09-9
TIERED APPROACH
TO CORRECTWE
)
(Rulemaking-Land)
ACTION
OBJECTIVES
)
(35
III. Adm.
Code 742)
)
PRE-FILED
TESTiMONY OF
THOMAS
C.
HORNSUAW
Qualifications
My
name is Thomas
C.
Hornshaw.
I
am a Senior
Public Service
Administrator
and
the Manager
of
the Toxicity
Assessment
Unit of
the Illinois
Environmental
Protection
Agency
(“Agency”)
I
have
been
employed at the
Agency
since
August
of 1985,
providing
expertise
to
the Agency
in
the area
of environmental
toxicology.
Major
duties of
my
position
include
development
and
use
of procedures
for toxicity
and risk
assessments,
review of
toxicology
and
hazard
information
in
support of
Agency
programs
and
actions,
and
critical review
of risk assessments
submitted
to
the
Agency
for various
cleanup
and
permitting
activities.
I
was a
member
of the Agency’s Cleanup
Objectives
Team
until
February
of
1993,
when
that
Team’s
responsibilities were
assumed
mainly
by
the
Toxicity Assessment
Unit,
I
was also a
member of
the
Groundwater Standards
Technical
Team during
the
development
of the
Groundwater
Quality
Standards.
These two
teams
have
looked in
depth
at the
problems
involved
with
determining
acceptable
residual concentrations
of
chemicals
in
soil
andlor
groundwater-
I
have
also
participated
in
the
development of
the original
35
IlL
Adin.
Code
Part 742 rule,
Tiered Approach to
Corrective
Action Objectives
(“TACO”;
R97-14)
and
subsequent
amendments
to this rule.
1
I
received
Bachelor
of Science (with
honors) and
Master
of Science
degrees
in
Fisheries
Biology from
Michigan
State
University.
East Lansing,
Michigan.
I
also
received
a dual
Doctor
of
Philosophy
degree from
Michigan State
University,
in Animal
Science
and Environmental
Toxicology.
I am
a
member
of
the
Society
ofEnvironmental
Toxicology
and Chemistry
and
Sigma
Xi,
the
Scientific
Research
Society.
I have
authored
or co-authored
six papers
published in peer-reviewed
scientific
journals,
one report
issued
through
the
US.
Environmental
Protection Agency,
and have
written
or
co-written six
articles
which have appeared
in trade journals.
I
have
also presented twenty-one
posters
and/or talks describing
facets
of my
graduate work and
my
work at
the
Agency
at
various
regional and national
meetings.
A
more
descriptive
account of
my work and
educational
background
and
a
list
of
publications,
posters,
and talks
is
included
in
a
Curriculum
Vitae
presented
as Exhibit
1
to
this
testimony.
Testimonial Statement
It
has
recently
come
to the
Agency’s attention
that the
procedure
specified
in
TACO
currently for the determination
of area
background for
groundwater at
Section
742.410(b)(l),
the
“Prescriptive
Approach,”
is
now
out
of date
and must be
updated.
In
the
current
approach,
if
the data set
for
a
background
well
has no
more
than
15%
non-detect
results for
the
chemical
of
interest, is normally
distributed,
and has
at
least 10 sample
results, then
the area
background
concentration for
that chemical is
calculated as the
95%
Upper
Tolerance Limit
(“UTL”)
using the
calculation specified
in Section
742.410(b)(l)(C).
The Agency
selected
this
approach
at the
time
TACO
was first
proposed
because
this was the
approach recommended
by the
United States
Environmental
Protection
Agency (“USEPA”)
for
establishing
groundwater background
levels
at
RCRA
2
sites in “RCRA
Facility
Investigation
Guidance,
Interim
Final,”
EPA 530/SW-89-03
1
(May 1989)>
and its follow-up
document
“Statistical
Training Course
for
Ground-water
Monitoring Data
Analysis,” EPA 530-R-93-003
(1992).
Now,
however,
USEPA
has
developed
updated
guidance
for
determining
background
groundwater levels,
“Statistical
Analysis of Ground-water
Monitoring
Data
at
RCRA
Facilities-Unified
Guidance,”
USEPA,, Office
of Solid
Waste,
I
999c
(in
progress).
This
guidance
specifies
a
number of statistical
approaches
for determining
background
groundwater
concentrations,
with
the
approach
to
be
used dependant on
the
characteristics
of
the
data
set. It
is noteworthy that the
UTL statistic
is not among
the approaches
recommended
by
USEPA. It is
also
noteworthy
that
in
a remediation
project
overseen
by
the
Agency,
the responsible party
is
in
the process
of determining
the area
background
for
nitrate
in
groundwater,
in which the
UTL
will
eventually
be
calculated to
be in the
range
of
50-55
mg/I.
This concentration
of
nitrate is
also in
the
range at
which
potentially
serious
effects might be experienced
by
infants.
In
keeping with the updated
guidance,
the Agency
is
proposing in Errata
Sheet
Number I to update the
determination
of
area
background
for
groundwater
in Section
742.410. We
recommend removing
all
of the
current
subsection
742.410(b) and
replacing
it
with
a new
subsection
(b)
as follows:
(b)
Area
background
shall be
determined
by using
a
statistically
valid
approach
appropriate for
the
characteristics
of
the
data set that
is
approved
by
the
Agency.
This
concludes
my
testimony
on Errata Sheet
Number
1.
3
EXHB1T
1
CURRICULUM
VITAE
THOMAS
C.
HORNSHAW
EDUCATiON:
Ph.D., Animal
Science and
Environmental
Toticology,
1985. M.S.,
1981,
and
B.S.,
1976,
Fisheries
Biology, Michigan
State University.
EXPERIENCE:
Senior Public Service
Administrator,
Illinois
Environmental
Protection
Agency,
1985-
Present.
Graduate Research
Assistant, Department
ofAnirnal
Science, Michigan State
University,
1981-
1984.
Graduate Research
Assistant,
Department
of
Fisheries and Wildlife,
Michigan State
University,
1978-
1981.
Student
Aide,
Water
Quality
Division, Biology Section,
Michigan
Department
of
Natural
Resources,
1976- 1977.
FiELDS
OF
EXPERIENCE:
AE
the illinois
Environmental
Protection
Agency, Dr.
Hornshaw’s
major
duties include
the management
of the Toxicity
Assessment
Unit;
development
and
use
of
procedures
for human
and
environmental
exposure
assessments
and
risk
assessments;
review of
toxicological
data
and
hazard
information
in
support
of
Agency programs
and
actions;
and
critical
review
of
remedial
investigation
and
risk
assessment
documents
submitted to the
Agency
during
hazardous
waste
site
investigations
and cleanups. Dr. Hornshaw
was
a
member
of
the
Agency’s
Cleanup Objectives
Team
until
1993,
when that Team’s
functions
were
assumed
by
the
Toxicity Assessment
Unit. As
a
member
of
Agency work
groups,
he
participated in
the
development
of
ilhinois=
Air
Toxics,
Groundwater
Quality,
and
Tiered
Approach
to
Corrective
Action
rules.
He is
one of the
Agency’s
representatives
to
the
Great
I.akes
Toxic
Substances
Control
Agreement
(member
of
the
Fish
Advisory
Task
Force)
and
is
the
Chair
of
the
multi-agency Illinois
Fish
Contaminant
Monitoring
Program. Dr.
Hornshaw
was
also a
member
of
the
National
Advisory
Committee
for
Acute
Exposure
Guidance
Levels,
moderated
by
USEPA, whose task
is
the development
of action
levels
for
use
in
unplanned
air
releases
of
hazardous
chemicals.
In an earlier
assignment at
the Agency,
Dr. Hornshaw
assisted
in
the
development
of bioassay
protocols
and quality
assurance
procedures
for the
Biomoniroring
Unit.
As
part of
his
duties
during
his
Ph.D- research
at Michigan
State University,
Dr. Hornshaw
conducted
experiments
to
develop protocols
for mammalian
wildlife
dietary
LC
50 and
reproduction
tests,
using
mink
and
European
ferrets
as representative
mammalian
carnivores. He
has
published
four
papers in
scientific journals as
a result of
this
research, and the
protocols developed
from
these
studies
have
been
published
by
USEPA.
As
part of
his
duties
during his
M.S. research
at
Michigan
State,
Dr.
Homshaw
conducted
experiments
to
assess
the
suitability
of
several species
of
Great Lakes
fish for
animal feed,
testing the
fish
in
reproduction
trials
with mink. He
quantitated levels
of polychiorinated
biphenyls in
fish,
mink
fat,
and
mink
milk
as
a
portion of
this research,
and published the
results
of
these studies
in
a
scientific
journal.
These
results
were also
published in
several trade
journals serving
the fur industry.
He
has
authored or
co-authored
articles detailing
the
results
of several other
studies
sponsored
by the
fur
industry
in these trade journals.
After
receiving his Bachelors
degree from
Michigan
State, Dr.
Hornshaw
worked
as a student
aide
in
the
Biology
Section of the Water
Quality
Division
of
Mic.higans
Department
of Natural
Resources.
His duties included
assisting
staff
aquatic
biologists
in the collection
of fish, water,
sediment,
and
benthos
samples, in
laboratory
work, in data
handling,
and in
reporting
requirements.
His
field
experience included
sample collection
and
identification
from inland
lakes,
Great Lakes,
and
rivers
and
streams.
HONORS:
Bachelor of
Science, with honors;
Member,
Sigma
Xi,
the
Scientific Research
Society.
AFFILIATIONS:
Member,
Society
of Environmental
Toxicology
and
Chemistry.
THESES:
Horrishaw,
T. C.
1984.
Development
of
Dietary
LC
50 and
Reproduction
Test Protocols
Using
Mink
and Ferrets
as
Representative
Mammalian
Carnivores.
Ph.D.
Thesis,
Michigan
State University,
East
Lansing,
Ml. 2l
2
pp.
V
Hornshaw,
T.
C.
1981.
Renewed
Use of
Underutilized
Species
of Great
Lakes
Fish for
Animal
Feed.
M.S.
Thesis,
Michigan
State
University,
East
Lansing, MI.
45pp.
PUBLICATIONS
(Peer
Reviewed):
Ringer,
R. K., Hornshaw,
T.
C.,
and
Aulerich, R.
J.
Mammalian Wildlife
(Mink and
Ferret)
Toxicity
Test Protocols
(LC
5
Q,
Reproduction,
and Secondary
Toxicity). U.S.
Environmental Protection
Agency
Report No.
EPA/600/3-91/043,
July
1991.
NTIS Document
#
PB91-216507.
Hornshaw,
T.
C.,
Aulerich, R.
J.,
and
Ringer, R. K.
1987. Toxicity of
thiram
(tetramethyhhiuram
disulfide) to
mink and European
ferrets. Bull.
Environ.
Contam.
Toxicol.
38: 618 - 626.
Mornshaw,
T.
C.,
Ringer,
R. K.,
Aulerich,
R.
J.,
and
Casper,
H. H.
1986.
Toxicity of
sodium
monofluoroacetate
(Compound
1080)
to mink
and European ferrets.
Environ.
Toxicol.
Chem.
5:
213-223.
Horrishaw,
T. C., Aulerich, R.
1.,
and
Ringer,
R.
K. 1986.
Toxicity
of o-cresol
to mink
and
European
ferrets.
Environ.
Toxicol. Chem.
5:
713 -720.
Hornshaw,
T. C.,
Safronoff,
J.,
Ringer,
R. K, and Aulerich,
R.
J.
1986. LC
50
test
results
in
poiychlorinated
biphenyl-fed
mink: age,
season, and
diet comparisons.
Arch.
Environ.
Contam.
Toxicol.
15:
717 - 723.
Bleavins,
M. R.,
Aulerich,
R.
J.,
Hochstein,
J.
R.,
Hornshaw,
T.
C.,
and Napolitano,
A.
C.
1983.
Effects
of excessive
dietary
zinc
on
the
intra-
uterine
and postnatal
development
of
mink.
J.
Nutr.
113:
2360-236?.
Hornshaw,
T.
C.,
Aulerich,
R.
J.,
and
Johnson,
H.
B.
1983.
Feeding
GTeat
Lakes
fish
to mink:
effects
on
mink
and
accumulation
and
elimination
of
PCBs
by
mink.
J.
Toxicol.
Environ.
Health
11:
933
-
946.
PUBLICATIONS
(Trade
journals):
Hornshaw,
T
1992.
illinois’
Air
Toxics
selection
process
described.
National
Air
Toxics
Information
Clearinghouse
(NATICH)
Newsletter.
USEPA
Office of
Air
Quality
Planning
and
Standards,
Research
Triangle
Park,
NC.
January,
1992.
Aulerich,
R.
J.,
Napolitano,
A. C.,
and
Hornshaw,
T.
C.
1986.
How
supplemental
copper
affects
mink
kit
hemoglobin
concentration.
in
The
Fur
Rancher
Blue
Book
of Fur
Farmjg.
Communications Marketing,
Inc.,
Eden
Prairie,
MN.
pp. 42
- 46.
Hornshaw,
T.
C.,
Aulerich,
R.
3.,
and
Ringer,
B..
K.
1985.
Mineral
concentrations
in
the
hair
of
natural
dark
and
pastel
mink.
Scientifir
9(3):
216
- 219.
Aulerich,
K.
J.,
Napolitano,
A.
C.,
and
Hornshaw,
T. C.
1985.
Effect
of
supplemental
copper
on
mink
kit
hemoglobin
concentration.
Fur
Farmer’s
Gazette
of
the United
Kingdom
35(4):
8
- 11.
Hornshaw, T.
C.,
Aulerich,
R.
J.,
Johnson,
H.
B.,
and Ringer,
R.
K. 1982.
How
suitable
are
todays
Great
Lakes
fish
for use
in
feeding
mink?
Fur
Rancher
62(9):
21
- 23.
Hornshaw,
T.
C.,
and
Aulerich,
R.j.
1980.
Can
Great
Lakes
fish
again
be
fed
safely
to mink?
In
The
xir
Rancher
Blue
Book
of
Fur Farming.
Communications
Marketing,
inc., Eden
Prairie,
MN.
pp.
48
.49
PRESENTAT!
ONS:
Hornshaw,
T.C.
“The
illinois
Fish
Contaminant
Monitoring
Program”
Talk
presented
at
the
27
th
Annual
Fall
Meeting,
Midwest
Regional
Chapter,
Society
of
Toxicology, November
7,
2008,
Downers
Grove,
1L.
Hornshaw,
T.C.
“illinois
EPA
Pilot
Study:
PPCPs
in
Illinois
Drinking
Water.”
Talk
presented
at
the
Meds
with
Water...Not
in
Water
Pharmaceutical
Summit
Conference,
October
1,
2008,
Springfield,
IL.
Willhite,
M.
and
Hornshaw,
T.
“Illinois
EPA
Study
of
Pharmaceuticals in
Drinking
Water.”
Talk
presented
at
the Illinois
Wasts
Management
and
Research
Center
Symposium
on Pharmaceuticals
and
Personal
Care
Products
(PPCPs)
in
the Illinois
Environment,
April
25,
2008,
Champaign,
IL
Hornshaw,
T.C.
“Emerging
Contaminants:
What
Next
to Worry
About?”
Talk
presented
at
the
Illinois
Lake
Manage rnent
Association Annual
Conference,
February
28-29, 2008,
Springfield,
IL
Hornshaw,
T.C. and Homer,
D.
LCaIumet
Ecotox
Protocol:
Protecting Calumer’s
Plants,
and
Animals.”
Talk presented at
the Calumet
Research Summit,
January 10-11,
2006,
Hammond,
IN.
Hornshaw,
T.C.
‘Background
Metals
and
PARs - Panel
Discussion.”
Session
Chair
and
Panel
Member
at the
Midwestern
States
Risk Assessment
Symposium,
August 25-27,
2004,
Indianapolis)
IN.
Hornshaw,
T.C.
Intrusion
Action Levels
- Panel
Discussion.”
Panel Member
at
the
Midwestern
States Risk
Assessment
Symposium,
July
24-26,
2002,
Indianapolis, IN.
Hornshaw,
T. C.
AThe
illinois
Strategy
for
Endocrine
Disruptors.@
Talk presented
atThe
Endocrine
Disruptor
Debate: Environmental
Chemicals
and
Reproductive
and
Developmental
Health,
October
17, 1997.
St. Paul, MN.
Hornshaw, T. C. ARisk
Pathways and Exposure
Potential
as
Critical
Factors
in
the
Determination
of
Remedial
Objectives.@ Talk presented
at
the Science
for
Environmental
Professionals
and
Attorneys
Conference,
january 8,
1997,
Chicago, IL.
Hornshaw,
T.
C.
APotential
Health Effects
of Triazine
Herbicides
and Their
Metabolites
in
Community Water
Supplies.@ Talk presented
at
the
1996
Illinois
Agricultural
Pesticides
Conference,
January
3-4,
1996,
Champaign,
IL.
Hornshaw,
T.
C.
‘The
Illinois
Fish
Contaminant
Monitoring
Program.” Talk
presented
at
the
Biannual
Meeting
of
the
Federal-State Toxicology
and Risk
Assessment
Committee
(FSTRAC),
November 6-8,
1991,
Chicago,
IL.
Hornshaw,
T.
C. ‘Assessing
Exposure
to Toxic Air
Releases from
a Chemical Facility:
Illinois
Acrylonitrile
Exposure Assessment.’
Talk presented
at the National
Governors’
Association
Conference
on
Assessing
Exposure
to
Toxic
Contaminants:
Issues
and Problems Facing
State
Government,
March
29, 1989,
Salt Lake
City,
UT.
Horoshaw, T.
C.
“Risk Assessment from
State Point
of View.”
Talk presented
at
the
1st
Annual
Hazardous
Materials
Management
Conference/Central,
March 16,
1988,
Chicago,
1L.
Perino,
1.
V.,
Whitaker,
J.
B.,
and
Hornshaw, T.
C.
Technical
aspects
of an
aquatic
toxicological
testing program
at a state regulatory agency.
Poster
presented
at the
1st Annual Meeting
of the
Ozark-
Prairie Chapter
of the
Society of
Environmental
Toxicology
and
Chemistry,
April
24-26,
1986,
Columbia,
MO.
Hornshaw,
T.
C.
“illinois
EPA’s Aquatic Toxicity
Testing
Program.” Talk
presented
to
the
illinois
Environmental
Consensus
Forum.
December
12,
1985. Springfield,
IL.
Aulerich, R.
J.,
Bursian,
S.
J.,
Nachreiner,
R.
F.,
Olson,
B. A., Hochstein,
J.
R.,
Hornshaw,
T.
C., and
Koudele, K
A.
Toxicological
manifestations
of
dietary
exposure
to
3,4,5,3,4’,
5’. hexachlorobiphenyl
in
mink.
Poster
presented at the
24th Annual
Meeting
of
the
Society of Toxicology,
March
18-22,
1985, San
Diego,
CA.
Hornshaw,
T.
C.
“Effects
of Feeding
Great
Lakes
Fish
to
Mink.
Talk presented
at the
Great
Lakes
Commercial
Fisheries
Workshop,
March
12,
1985,
Mackinaw
City,
Ml.
Hornshaw,
T.
C.,
Safronoff,
j.,
Aulerich,
R.
J.,
and Ringer,
R.
K.
Development
and
validation
of
dietary
LC
50
test
protocols
for wildlife
mammalian
carnivores
using
mink and
ferrets.
Poster
presented
at the 5th
Annual
Meeting
of
the
Society
of Environmental
Toxicology
and
Chemistry,
November
4-7,
1984,
Arlington,
VA.
Hornshaw,
T.
C.,
Ringer,
R.
K,
and Aulerich,
R.
J.
Toxicity of thiram
to
mink
and
European
ferrets.
Poster
presented
at
the 23rd
Annual
Meeting
of
the
Society
of Toxicology,
March
12-16,
1984,
Atlanta,
GA.
Horrishaw,
T.
C.,
Ringer,
R. K.,
and
Aulerich,
R.
J,
Toxicity
of
sodium
monofluoroacetate
(Compound
1080)
to
mink.
Poster
presented
at
the
22nd
Annual
Meeting
of the
Society
of
Toxicology,
March &11,
1983,
Las
Vegas,
NV.
Hornshaw,
T.
C.,
Aulerich, R.
j.,
Johnson,
H.
E.,
and Ringer,
R. K Suitability
of
today’s Great
Lakes
fish
for
animal
feed. Poster
presented
at the
International
Symposium
on
PCBs in
the
Great
Lakes,
March
15-17,
1982,
East Lansing,
Ml.
BEFORE THE
ILLINOIS
POLLUTION
CONTROL
BOARD
IN THEMATTER
OF:
)
CVED
PROPOSED
AMENDMENTS
TO
)
NOV
j
TIERED
APPROACH
TO CORRECTIVE
)
R09—9
ACTION
OBJECTIVES
)
(35
IlL
Adrn. Code 742)
)
PRE-I?ILED
TESTIMONY
OF
GARY
KING
Oualifications
My
name
is
Gary
King. I
am
the Acting
Chief
for the
Bureau of
Land
at
the Illinois
Environmental
Protection
Agency. Since 1990,
1
have
been
senior manager
for the
Illinois
EPA
site
cleanup programs: the
voluntary cleanup
program,
federal and state
Superfund
cleanup
programs,
Department
of
Defense
cleanup
program,
Brownflelds
assistance
program
and
the
Leaking
Underground
Storage Tank program.
I led
illinois
EPA’s
development
of
the
original
35
III.
Mm.
Code
Part
742
rule,
Tiered
Approach
to
Corrective
Action
Objectives
(TACO,
R97-l4)
and all
subsequent amendments.
I
also chaired
the
Association
of
State and Territorial
SoTid
Waste
Management
Officials
(“ASTSWMO”)
CERCLA Research
Center
from
January
2001 to October
2008.
In
that
role
I
had
frequent contact
with
other States and
U.S
EPA concerning
important
issues
to
State
and
federal
Superfund
programs.
Prior
to
1990, I
managed
Illinois
EPA
land
enforcement
programs.
I am
an
attorney
and
hold a B.S
degree
in civil engineering
from Valparaiso
University.
Testimonial Statement
I will
be
testifying in
support
of
the
proposed
amendments
to
35
Ill. Adnt
Code
742:
Tiered
Approach
to Corrective
Action
Objectives.
I
will present
an overview
of
the
pathway
I
evaluation and
tiered
approach
to the indoor
inhalation
exposure route; describe
the
derivation
of
the Tier
1
remediajion
objectives
for
the indoor
inhalation
exposure
mute,
including
the
recommended parameter
values
for the modified Johnson
and
Ettinger
(J&E) model;
and
explain
the
rationale and requirements
for the
use
of
soil
gas data and
building control technologies.
Subpart
A: Introduction
Section
742.115 introduces
the exposure
routes to
be evaluated
under
this
Part,
including
the
indoor inhalation
exposure
route. Similar
to the
groundwater
ingestion route,
the
indoor
irthalation route has
both a soil and
groundwater component.
In
addition,
it has
a
soil
gas
component.
The
soil
component is the
migration of
contaminants from
soil
through
soil
gas
into
a
building
interior.
The
groundwater
component is
the migration of
contaminants from
groundwater
through soil
gas into a
building
interior. This pathway
is
unique
in that
it
involves
three types
of
media:
soil,
groundwater,
and soil
gas.
SubDart
B: General
Section
742.200
contains
new
definitions
for
the
terms
“building,”
“building
control
technology,”
“soil gas,” and
“soil
vapor
saturation limit.”
Assigning
a specific
meaning
to
“building”
will
avoid
confusion
as to
whether
the indoor
inhalation pathway
must
be evaluated
for every
structure.
The
use
of
“building
control
technology”
describes
mitigation
systems for
indoor
inhalation risks and
is
compatible
with
the
existing
term
“engineered
barriers”
“Soil
gas”
merits a
definition now
that
it
has become a
medium
of
interest
as does
“soil vapor
saturation
limit,”
which parallels
the definitions
of “soil saturation
limit”
and “solubility.” The
amended
definition
of “soil
saturation
limit”
is
actually
language
taken
from
an
original footnote
contained
in
Appendix
B,
Tables
A and B. The footnote
offered the better
explanation.
As for the
amended
definition
of
“volatile
cbeinicals”
it
resulted
from a
re-examination
(and
eventual
deletion)
of
2
the
original
definitions of
“volatile
organic
compounds” and
“volatile chemicals.”
Today
the
term
is used to
define
contaminants subject
to
evaluation
under
the
indoor
inhalation
exposure
route,
including elemental
mercury.
Section
742.210
contains
19 new
incorporations
by
reference.
The most
notable
of
these
are
U.S. EPA’s
draft
guidance,
Evaluating
the
Vapor Intrusion
to Indoor Air
Pathway
from
Groundwater
and
Soils, which established
the use of
the
J&E model,
and
its
companion
document,
Users
Guidefor
Evaluating
Subsurface
Vapor Intrusion
into
Buildings,
which
provided
justification for certain
parameter
values.
Other
significant publications
include
ASTM
International’s Standard
Practice
for
Assessment
for Vapor
Intrusion
into Structures
on
Property
Involved
in Real Estate
Transactions
and the
Interstate
Technology
and
Regulatory
Council
(ITRC)’s
Vapor
Intrusion Pathway:
A Practical
Guide. Additional
incorporations
have
been
included
to
provide
soil gas
analytical
methods, source
information for parameter
value
selection,
and techniques for
mitigation systems.
Section
742.222
provides
methods
for determining
the soil vapor
saturation
limit and
parallels
Section
742.220,
which is used for determining
the soil
saturation
limit. The
soil
vapor
saturation
limit
is
the
maximum
vapor
concentration that can
exist in
the soil
pore air at
a
given
temperature
and
pressure.
Section
742.Appendix
A,
Table
K
presents the
soil vapor
saturation
limits for
volatile chemicals.
For the
indoor
inhalation exposure route,
soil
gas
remediation
objectives
cannot exceed
the
soil vapor
saturation limit;
otherwise, the
assumptions
of the
modified J&B
model would
be
violated.
The
modified J&E model
as
well
as
the
existing
RBCA
and
SSL
models operate on similar
assumptions
regarding
soil
saturation
and
solubility.
These
risk-based
models assume
an equilibrium
between
contaminant
concentrations
that
exist
as
vapors
in
soil
pores, contaminants
that
adhere
to
soil
particles,
and contaminants
that dissolve
3
into
water within
soil pores.
In
Section
742.225, compositing
and averaging
of
sample
results
are
not allowed
to
demonstrate
compliance with the
indoor inhalation exposure route.
Compositing
of volatile
chemicals
is
already prohibited
under
this
Section
(the
physical
mixing
of
samples
in
the
field
provides
a
mechanism for the contaminants
to
volatize
and escape into the
atmosphere;
subsequent sample
analyses
would underestimate the amount
of contamination actually
present
at a site).
As for sample averaging,
first,
and
most important,
is the concern that
averaging
could
allow
a
‘hot spot” of contamination
to remain
beneath
a building
that
could result
in
a
concentrated ‘slug” of chemicals entering the
building
in a
relatively short period
of time. It
is
possible under such conditions
that
these short-term,
higher-level concentrations
could result
in
odor,
irritation, and even central nervous system (headache,
nausea,
etc.)
problems.
Second,
it
is
unlikely
that a sufficient number
of
soil a.ndlor
groundwater samples will
be collected
for
the
indoor inhalation
exposure route to allow
for the
development
of
statistically valid 95 percent
upper confidence
limits
(UCLs)
for
this
route. Third, an
appropriately
conducted indoor
inhalation
exposure evaluation
would
typically include
sampling
in
two
or more
seasons, and
procedures for
deriving the
most
representative statistic for such data
sets can be
problematic.
For
these reasons, illinois
EPA
decided that averaging for the
indoor inhalation route
would not
be
included,
except in Tier 3.
Nonetheless,
we
would be willing to evaluate an
averaging
methodology
if it
adequately
addressed
the
concerns we have
raised.
Illinois EPA
acknowledges
that
there are likely
to.be
site-specific
circumstances in
which
averaging
results
would
be appropriate,
and
that
an
outright
prohibition against averaging
is
not
needed. Therefore, Section
742.225(b)(5)
allows for averaging
in Tier
3
based upon
an illinois
EPA-approved plan.
4
Section 742.227
provides
minimal requirements
for
the
collection
and
analysis
of soil
gas
samples.
Ordinarily, sampling
locations,
quantities
and
protocol
are determined
by the
program
under which
the
remediation
is being
performed
(LUST, RCRA.
Site Remediation
Program);
however,
because the use
of soil gas data
is
not
as well
understood
by
site
evaluators,
Illinois
EPA decided
to specify
the
most
essential criteria
to reduce
the likelihood
of
error,
the
misrepresentation
of
actual conditions,
and the need
for repeat
sampling.
Sihart
C: Exposure
Route
Evaluations
Section 742.3
12
identifies ways in which
the
indoor
inhalation
exposure
route
may
be
excluded from consideration.
Indoor inhalation
presents
a
risk only
if
volatile chemicals
are
the
contaminants
of
concern. If a
site has none
of
the
59
chemicals
listed in Section
742.Appendix
A,
Table
I
or
any
other
contaminants meeting
the new
definition
of
“volatile
chemicals,”
then
the
indoor inhalation
pathway
does not
need to be evaluated.
If
volatile
chemicals
are present,
the site evaluator
has the option
of excluding
the
pathway
by
either
restricting
buildings
above
contaminated
areas
or
by
implementing
building
control technologies.
The
general
pathway
exclusion criteria
of
existing
Sections
742.300
and
742.305
must
also be
met; these are
the “speed
bumps”
to
prevent
free product,
the leaving
behind
of
materials
with the potential
impact
of
hazardous waste,
and concentrations
of
polychiorinated
biphenyls
above 50
parts
per
miflion.
The new
building-specific
exclusions would
need
institutional controls
as
follows:
I.
A
land
use
restriction
prohibiting
a
building
or man-made
pathway
above
the
contaminated
soil
or
groundwater.
(The
indoor inhalation
exposure route
is
incomplete
if a building
does
not
exist.)
2.
Operation and
maintenance
requirements
for
approved
building
control
5
technologies, including
sub-slab
depressurization,
sub-membrane
depressurization
or
membrane
barriers. These
requirements
are contained
in the new
Subpart
L:
Building
Control Technologies.
The indoor
inhalation exposure
route
cannot
be excluded
by
use
of
a
groundwater
ordinance. This exclusion
is
not
allowed because
an ordinance
restricting
the
use
of groundwater
as a
source of
drinldng water would
not protect
the enclosed
air space
of
a
building from
the
migration
of
contaminants
emanating
from
the
groundwater.
Subpart E:
Tier
I Evaluation
A
Tier
1
remediation
objective
is
a
numerical chemical concentration
that
represents
a
level of
contamination
at
or below
which there are
no human health
concerns.
Sites
achieving
residential
Tier 1
remediation
objectives are
intended
to
clearly indicate
that the
property
meets
an
unrestricted
land use category
for that category
of use,
Tier
I requires a
determination
of
either
residential or
industriallcornmercial
land use. Generally,
equally protective
but less
restrictive
remed.iatiori
objectives
apply
to the
industrialJcornrnercial
sites. [Note:
whenever
remediation
objectives are
based
on
an industriallcommercial
land
use,
an institutional
control
rnustbe
placed on
the
property
in
accordance
with
Section 742.1000(a)(i).]
Early
in
the rulemaking
development,
SRAC
proposed
that
indoor
air OSHA standards
should
apply in lieu of
TACO
at facilities
where
the chemicals
of
concern
continue to
be used
or
manufactured.
Illinois
EPA disagreed
since vapor
intrusion
potentially
impacts the entire
building
and all of
its
occupants.
The
OSHA
standards
may
be more narrowly
applied
to
a
subset
of
workers
and do not account for
the future use
of
the property.
As with
the
other
exposure routes, the
indoor inhalation
remediation
objectives are
calculated
based on
a one-in-a-million
individual excess
cancer
risk
for chemicals
causing
6
carcinogenic
adverse
health
effects
and a
hazard
quotient
of one
for chemicals
causing
noncarcinogenic
adverse health
effects.
Risk-based indoor inhalation
remediation
objectives were
derived from
equations
combining
exposure
assumptions
with
toxicity
data. The steps
used
to
develop the
soil1
gToundwater and
soil
gas remediation
objectives
included:
1.
Calculating
a concentration
ofthe
contaminant
of
concern in
indoor
air that
adequately
protects
humans
who
inhale this air (i.e.,
meets the above
mentioned
risk criteria);
2.
Calculating
an
acceptable
concentration
of the
contaminant
of concern
in the
soil
gas at the
source
of
contamination.
This
concentration
will
not cause the
contaminant
in
indoor ar to
exceed
the
concentration
calculated
in Step 1.
This
calculation was
made using
an attenuation
factor derived
from
a
mathematical
model developed
by Johnson and
Effinger
(J&E).
[Note: the ratio
of the
concentration
in the
indoor
air
(Step
1)
to
the
soil gas
concentration is
called
the
attenuation
factor.
Thus the primary
use
of
the
J&E
model is
to
calculate
the
attenuation
factor.]
3.
Calculating
acceptable
soil
and
groundwater
remediation
objectives using
the
soil
gas remediation objective
calculated
in Step
2,
with
the
assumption
that this
contaminant
is
in
three
phase
equilibrium.
The
J&E
model is
preferred
by
U.S.
EPA
and
is the
most common predictive
model
used
by
State
environmental
agencies in
calculating the
attenuation of
contaminant
concentrations
from
the subsurface
to
indoor
air. The
attenuation
factor
accounts for the following
processes:
7
1.
Migration
of contaminants
from the source
upwards
through
the
vadose
zone.
The
source
of
contaminant
concentrations
in
the subsurface
may
be
either
soil
or
groundwater.
If
the
source is groundwater,
the attenuation
factor
considers
the
initial migration
of
contanilnants
through
the
capillary
fringe.
2.
Migration
of
contaminants
through
the
dirt
filled
cracks in
the
slab-on-grade
or
basement
floor.
3.
Mixing
of
the contaminants
with
air
inside
the
building.
Dr. Atul Saihotra,
RAM Group,
will
provide testimony
on
the scientific
basis,
fundamental
concepts
and
application
of
the
modified
3&E
model.
Illinois
EPA
provides
IS
J&E
equations
and
56
default
parameter
values
(Section
742.Appendix
C, Tables
L and
M).
Exposure
factors
are consistent
with
the
values
used
in
the
current TACO
regulations.
Toxicity
factors were
obtained
using
U.S.
EPA’s hierarchy
and are
chemical-specific.
Existing
Sections
?42.5O5(b)(3)
and
(4),
which
contain the
procedures
for
addressing
the
additive
effects of
similar-acting
chemicals
in
developing
Tier
1 groundwater
remediation
objectives,
also apply
to the
indoor
inhalation
exposure
route.
Tier
1
remediation
objectives
have been
developed
for
a
slab-on-grade
building.
A
slab-
on-grade
building
is
a
more
conservative
scenario
because
there is
less
air
available
in
the
building to
mix
with
the
contamination.
A
building
with
a
basement
assumes
there
is
mixing
of
the
air between
the
basement
and the
first floor. Tier
I remediation
objectives
are
applicable
to
both
slab-on-grade
buildings
and
buildings with
basements.
A
slab-on-grade
building is
one with a
concrete
floor
at about
the same level
as
the
grade
of
the
surrounding
area;
a
basement
would
tical1y
be below
the
grade
of
the
surrounding
area.
Tier
1
indoor
inhalation
rernediation
objectives
calculated
for
a
slab-on-grade
building are
not
8
much
lower
than what would be developed
for a
similar building
with a
basement.
For
ease
of
implementation,
illinois EPA
chose to use
only
one
set
of
Tier
1
remediation
objectives.
Building-specific
default
values
for
the following
parameters
were used
to develop
the
Tier
1 remediation
objectives: length
of
building
),
9
(L
width of
buIlding
(W
8
),heIght
of
building
(H
8
),surface
area
of
enclosed
space
at
or below
grade
(A
8
),
and
building
ventilation
rate
(Qb).
The same default
values must
be used for the same
parameters when
performing
Tier 2
calculations.
The
actual values
of these
parameters
do not
have
a great impact
on the
remediation
objective;
however,
the
default
values
are
based
on a
conservative representation
of
the
type
of
buildings
that
are
or may
be
present at
the
site
in
the
future.
Without
these
conservative
values,
restrictions
would be required
on
the
minimum
size of a
building that can be
constructed over
the
contaminated
area.
For
the indoor inhalation exposure
route,
the industriallcomrnercial
remediation
objective
differs from
the residential
remediation
objective
in
three
ways: exposure
duration,
building
size,
and air
exchange rate. The air
exchange rate (ER)
is
used
to represent
the
mixing
that
occurs
within
a
building. The
air
within a residence
is
assumed
to be
flushed
out
of the
building
at a
rate
of
13.8
times
per day
(0.53
times per
hour)
and
at a
commercial
location at
the
rate
of
22.32
times
per
day (0.93
times per hour)
based on values
listed
by Hers et aL
(2001)
and Murray
and
Burmaster
(1995).
These two
papers are
the source
of
the recommendations
in
U.S. EPA’s
User
‘s Guide for
Evaluating Subsurface
Vapor
Intrusion il2to
Buildings (2004).
Tier
1
indoor
inhalation remediation
objectives
assume
the vadose zone
is composed
of
sand.
The default properties
used are
consistent
with the
existing TACO values
for
sand.
For the I&E equations,
illinois
EPA used
a chemical-specific
value for
Dimensionless
Henry’s Law Constant
set to a
default system
temperature of
13°C.
U.S.
EPA’s
draft
vapor
9
intrusion
guidance
— as well
as
the other
exposure routes
in
TACO
— set the
system
temperature
for
Dimensionless
Henry’s Law Constant
at
25°C.
Illinois EPA decided
to use
a lower
system
temperature
for
the
indoor
inhalation
route in
Tiers
1
and
2
because it
is more representative
of
the
groundwater
temperature
in Illinois,
The
groundwater
temperature
in
Illinois
ranges
from
8.3°
C
to
16.7° C;
the
average
within
that range
is
13.190
C.
The lower temperature
reduces
the
Dimensionless
Henry’s Law
Constant, resulting
in
a
less stringent
remediation
objective.
The
States
of New Jersey and Michigan
also apply
a state-specific system
temperature
(13°
C and
12.5°
C,
respectively)
for Dimensionless Henry’s
Law Constant
under the indoor
inhalation
exposure
route.
Section 742.Appendix
B,
Table
G
provides
a
Tier
1 table
of
numerical
soil,
groundwater
and
soil
gas
values
for
both residential
and industrialJcommercial
receptors.
An Acceptable
Detection Limit
(ADL)
column is
also part
of
the indoor inhalation
Tier
1
table
and
applies
only
to soil
remediation
objectives.
The A.DL identifies
the
lowest
practical
quantitation
limit
of any
U.S.
EPA-approved
methodology for any chemical.
For
most
chemicals,
the
column
is noted
with
an asterisk,
meaning the detection
limit is
less than
the
remediation
objective.
Where
this
is
not
the
case, the
ADL
is
used
as
the
remedia±ion
objective. This
parallels
ADL
usage
on
the
existing
Tier
1 look-up
tables, Section
742.Appendix B,
Tables
A
and
B. Remediation
objectives
are
not
provided
for the construction worker
population
since this
receptor group
is
not
at
risk
from
indoor
inhalation
exposure.
The
exposure
duration for indoor
construction
in
almost
all
cases
is
less
than the
exposure duration
for the
residents
or commercial
workers. Thus
the
protection of
these
two receptors
will ensure
protection
of the construction
worker
during
the
period of
indoor construction.
In
addition
to
describing Section
742.Appendix
B, Table (3,
Section
742.515
explains
10
how
Tier
1 remediation objectives
for
the
indoor
inhalation
exposure
route are
to
be
used
in
regards
to
the
three
media
(soil,
groundwater
and soil
gas)
and in
conjunction
with
the
existing
Tier
I tables
for
the
other
exposure
routes.
During
the
migTation
of
contaminants
from
soil
and
groundwater
to
a
building’s
interior,
the
contaminants
must
pass through
soil
gas.
U.S.
EPA,
ITRC
and
individual
States
generally
concur
that
the
measurement
of
soil
gas
is
the
most
reliable
indicator
of
a
vapor
intrusion
threat.
However,
many
sites
will
collect
soil
and
groundwater
data
in
characterizing
the
other
exposure
routes
and
will
not want
to do
further,
and
potentially
unnecessary,
field
work.
For
these
reasons,
Illinois
EPA
proposes
that
sites
intending
to
use
numerical
rernediation
objectives
to
demonstrate
compliance
with
the
indoor
inhalation
exposure
route must
meet
either
the
1)
soil and
groundwater
remediation
objectives,
or
2) soil
gas
remediation
objectives.
The
use
of
indoor
air
data
to
demonstrate
compliance
with
remediation
objectives
under
Tier
1
or
2
was
rejected
early
by
Illinois
EPA.
Indoor
air
samples
are
highly susceptible
to
bias
from
occupant
sources
(smoking,
dry
cleaning,
household
chemical
use
and storage,
etc.).
They
•
are
also
invasive,
requiring
site
evaluators
to
obtain
access
to indoor
space.
The
rules
do
not
prohibit
the
use of
indoor
air
data;
however,
any such
request
would
be
a
Tier
3
evaluation.
Under
Tier
1,
separate
chemical-specific
remediation
objectives
are calculated
for each
route,
including
now
the
indoor
inhalation
exposure
route.
If
the
respective
Tier
1
remediation
objective
is not
exceeded
for
a
route,
the
user
may exclude
that
route from
further
investigation
(additional
exposure
routes
may
be excluded
under
Section
742.312).
Of
the
exposure
routes
remaining,
the
most
restrictive
or
health
protective
Tier
1 soil
and groundwater
remediation
objective
from
Section
742.Appendic
B, Tables
A,
B,
E, and
G
is to be
compared
tà
the
concentrations
measured
at
a
site.
This
practice
is
consistent
with
cunent
usage
of
the Tier
1
11
tables.
Subpart
G:
Tier
2
Soil Evaluation
Tier
2
remediation
objectives are
developed
using the
J&E
equations
provided
in Section
742.Appendix
C,
Table
L.
fllinois
EPA
is
preparing
a guidance document
for
site
evaluators
thai
will
describe
in
a more
complete
narrative
how Tier
2
equations
for the indoor
inhalation
exposure
route
will
work.
Tier
2
calculations
require
information
on the
physical
and chemical
properties
of the
individual
contaminants
at a
site. As in Tier 1,
a
chemical’s
toxicological
parameters,
physical
parameters
(obtained
from
Section 742.Appendix
C,
Table
E),
and
the
J&E
equations
themselves
may
not
be varied.
This
is
also
true
for
Tier
2
evaluations
applying the
SSL
and
RBCA
models
for the other
exposure routes.
Section
742Appendix
C, Table
M
contains
all
of
the parameters
used
for
the
J&E
equations.
These
parameters use either
default
values
(i.e,
standardized
and/or health
protective
values)
or actual
site-specific
field data. Where
default
values
are
provided,
they may be
used
in
Tier 2
equations.
That is, only partial site-specific
information need
be obtained
and
default
values
may
be
used for the
rest
of
an equation’s
parameter
inputs. This practice
is
consistent
with
Tier 2 evaluations for
the
other exposure routes.
For the indoor
inhalation exposure
route,
Tier
2
differs
from
Tier
1
in
two ways.
First,
the
additivity
of risk from
noncarcinogenie
contaminants
in
soil
must
be
taken
into
account
(as
required for the
other
exposure routes).
Second, the
attenuation factor
is based
on
site-specific
soil
properties,
including:
depth to
contaminated soil; types
of
soil present
beneath
the
ground
surface
and
the contamination source;
and
geotechnical
parameters
(dry soil
bulk density,
soil
total
porosity,
water-filled
soil porosity,
and
fraction
organic carbon content).
12
To determine
site-specific
physical
soil
parameters,
a
minimum
of one boring
per
0.5
acre
of
contamination
must be collected.
Each soil
sample analyzed
for
one
or
more
of
the
app licable
contaminants
of concern
must
also
be
analyzed
for water
content; at
sites
where
multiple samples
from
multiple
depths
are analyzed
for contaminants on
a dry weight
basis
and
their
volumetric
water content
can be measured
based
on
available
data, additional
samples
solely
for
analysis
of
water content
may
not
be
necessary.
Samples
for
geotechnical
data are
not required
from
directly under the building.
Samples
collected adjacent
to
a building are acceptable,
In
lieu
of
sampling
the different
soil
types
for
geotechnical
parameters,
use of the
default soil parameters
provided in
TACO
is
also
acceptable.
Soil
parameters
obtained
from
other
literature
searches and not
from
site-specific
determinations
may
be allowed under
Tier
3.
The depth
to
contaminated
media
D)
is
the
shortest distance
from
the
base
of
any
existing or
potential
building (or man-made
pathway into the
building)
to
a location
where
a
sample
result
exceeds
the
Tier
1
value
for a contaminant
of
concern
for the indoor
inhalation
exposure route.
It
is
essential
to
determine the
type
of soil
between
the
ground
surface and
the
contamination
source, as
the contaminants must
migrate
through
this soil before entering
a
building.
Ifthe
site stratigraphy varies
in
this
zone,
it should
be divided into
different layers.
For
each
different
soil
layer, the
soil
type,
thickness,
water-filled
soil
porosity
and
soil total
porosity
are
necessary
to
calculate
the
Tier
2 remediation objectives.
Specifically,
the
water-filled
soil
porosity and soil
total
porosity
are used
to estimate
the
effective
diffusion
coefficient
for
each
layer.
If
the
contaminated
medium
is groundwater,
then
the
capillary
fringe
is
included
as
one
of
the
soil
layers.
13
The
geotechnical
parameters — dry soil bulk
density, soil total porosity,
water-filled
soil
porosity, and
fraction
organic
carbon
content — are
used to estimate soil gas
concentrations
at
the
source,
assuming
that the
risk
being calculated
is
based
on representative
soil
concentrations.
Methods for determining
soil
parameters
for
the
indoor
inhalation exposure
route are
provided
in
Section
742
.Appendix
C,
Table
F.
The
most sensitive
parameters
are water content
and
thickness
of the capillary
fringe.
Fraction of organic carbon content
(f) is
also
sensitive;
increasing
f,
increases the
remediation
objectives. Depth
to
soil source is not sensitive because
the
modified
J&E model assumes
an
infinite source with no biodegradation
as the vapors
migrate through the vadose
zone.
Section 742.7 17 explains how the
J&E
equations
are
to be
applied when
calculating
soil
or
soil
gas
remediation objectives for the indoor
iithalation exposure
route.
Equations
J&El
through J&E3 are
used to
calculate the
acceptable concentration
of the contaminant
in
indoor
air.
Equation J&E1
applies only
to chemicals that cause carcinogenic health
effects, J&E2
applies
only to chemicals
that
cause noncarcinogenic health
effects,
and
J&E3
is
used
by
both
types
of
contaminants to convert from
parts per million
volume to milligrams per
cubic meter.
Estimation
of indoor air
remediation objectives
using J&El or
J&E2 requires two categories
of
input
parameters: toxicological information
and
receptor-specific
exposure
factors
(exposure
frequency, exposure duration and averaging
time).
Equation
J&E4
calculates
a
soil
gas
remediation objective using
the appropriate
indoor
air
remediation objective
(from
either J&El
or
J&E2) and an
attenuation
factor
developed
from
Equations J&E8b through J&ElS. The soil gas remediation objective
must
be compared
to
the
saturated vapor concentration
(Ct).
Section
741222
presents
the
methods
by
which the
concentration
is obtained;
for example,
site evaluators
may
use the list
of
values
in
Section
14
742Appendix A, Table K or calculate a site-specific
C
using
equation J&E6b.
If
the
calculated soil gas remediation
objective
is greater
than
C,
then
Ct
is
used
as
the
soil
gas
remediation
objective.
When comparing
the
calculated
soil
gas remediation
objective to soil
gas samples
from
the site, Section
742.717(k)
instructs
site
evaluators to use soil
gas
data
collected at a
depth
at
least three feet below the ground surfaee and above
the saturated zone. This
is
to
ensure
the
quality of
the
soil
gas
sample. Samples
taken less
than
three feet
from the
ground
surface
can
be
compromised
by
the
influence of barometric
pressure
fluctuations that
may cause an
influx
of
ambient air
into the
soil,
variations
in
ambient temperature,
and precipitation.
Samples
talcen
from
the
capillary fringe
or below are
unacceptable because
of high water saturation.
Equation J&E5 calculates
soil
remediation
objectives
using
an
equilibrium
conversion,
which assumes
that
the
soil gas is in
three
phase
equilibrium with
the
contaminated
soil
at
the
source.
This calculation takes
into
account
soil-specific
properties — water-filed
soil
porosity,
the
soil-water
partition coefficient, the air-filled soil
porosity, and the dry soil bulk density
— and
uses
a
chemical-specific Dimensionless Henry’s Law Constant
set
at a
system temperature
of
13°C (as in
Tier 1).
The calculated soil
remediation objective
must be compared with the
soil saturation
limit
(C).
Site-specific
C
values for the indoor
inhalation
exposure
route
may be calculated
using
equation J&E6a.
C1
values
for volatile
chemicals
for the indoor inhalation exposure
route
are
also
provided
in Section
742.Appendix
A,
Table
L.
This
table differs from
the
C
table
in
Section
742.Appendix
A,
Table A because it
uses different values
for two parameters:
the
system
temperature used
to
set
the
chemical-specific
Dimensionless
Henry’s Law Constant and
the
fraction
organic
carbon content
().
The soil
component
of
the
groundwater ingestion
exposure
15
route
(migration
to
groundwater
pathway)
and the
outdoor
inhalation
exposure
route
use
a
system
temperature
of 25°C. The
rationale
for the
difference
in
system
temperature
(13°
C
instead
of 25°
C)
for
the
indoor
inhalation
exposure
route
has
already
been
described.
As
for
differences
in
f
values,
the migration
to groundwater
pathway
uses
an
f
0.002
(mg/mg)
because
the
contamination
is moving
into
deeper
soils
with
a
lower organic
carbon
contenL
The
outdoor
inhalation
exposure
route
uses
an
f
value
of
0.006 because
the contamination
is
moving
up
through
the soils.
Illinois EPA
decided
to
use an
f
value
of
0.002
for
the indoor
inhalation
exposure
route
because
basements
are
below
surface;
using
a
lower
f
value results
in a
more
conservative
remediation
objective.
If the
calculated
soil
remediation
objective
is greater
than
C,
then
C
is
used
as
the
soil
remediation
objective.
This practice
is
consistent
with
the other
exposure
mutes.
Equation
J&E8b
is used to
calculate the
attenuation
factor. This
is
the
heart
of
the
predictive
model,
measuring
how
much contamination
from the
subsuthce
is
expected
to reach
the
indoor
air.
The
source
of the
contaminant
concentrations
in
the
subsurface
may
be
either
soil,
groundwater
or
soil
gas.
J&E8b
assumes
that
there
is no
significant
pressure
difference
between
the
subsurface
soil
and the building.
This
means that
contaminants
emanating
from
the
source
do
not
migrate
into the
building
by advection.
Migration
by
advection
is
represented
by the
parameter
Q,
also
known
as
the
volumetric
flow
rate
of soil gas
into the enclosed
space.
When
Q
is assumed
to
equal
zero
—
as
is
the case in Tiers
1
and
2
— diffusion
is
the
only contaminant
transport
mechanism.
This is analogous
to
the
indoor inhalation
model included
in the
Appendix
of the
Standard
Guide
for
Risk-Based
Corrective
Action
Applied
at Petroleum
Release
Sites that
assumes the
value
of
Q&i
is negligible
(ASTM
Designation:
E 1739-95).
If
advection
was
occurnng,
site
evaluators
would use equation
J&ESa to
calculate the
attenuation
factor
under
16
Tier
3.
The
remaining
equations,
3&E9a
through
J&El
8, are
used
to
establish
the
input
parameters
for
application
in J&E8b.
Equation
J&E9a
calculates
the
total overall
chemical-
specific
effective
diffusion
coefficient.
For
this
equation,
each
layer
of
soil (sand,
loamy
sand,
loam
etc.) through
which
contaminant
vapors
migrate
from
source
to
building
must
be
accounted
for.
The
total
thickness
of
the
soil
layers
must
equal
the
distance
from
the
bottom
of the
slab
to
the
top
of
the
contamination;
this relationship
is presented
in
equation
J&E9b.
The
distance,
called
the
source
to
building
separation
distance,
is
calculated
by
equation
J&ElO.
Equation
J&E1
1
calculates
the chemical-specific
effective
diffusion
coefficient
for each
soil
layer and
is used
in equation
J&E9&
Equations
J&E12a
and
12b
are used
to
calculate
the
surface
area
of
the
enclosed
space
at
or below
grade
through
which
vapors
enter
into
the
building.
For
slab-on-grade
buildings,
site evaluators
must use
J&E12a.
For
buildings
with
basements,
site
evaluators
must
use
J&E12b.
Equation
J&E13
calculates
the building
ventilation
rate
using
the air
exchange
rate
and
the
size
of the
building.
For
equations
J&El 2a,
J&El
2b
and
J&E13,
site
evaluators
must
use
the same
default
values
as in
Tier 1.
Equation
J&E14
calculates
the
area
of
total
cracks
assumed
to
exist
in
the
portion
of
the
structure
below
grade
through
which
contaminants
migrate
into
the
building;
default
values
from
Tier
1
must
be
used here
as
well. Contaminants
intrude
into thebuilding
only
through
cracks
that
completely
penetrate
the
slab;
these cracks
are
assumed
to
be
flied
with
dirt.
The
thickness
of
these
cracks
is
represented
by the
slab thickness,
which
is
set at
10
cm
for both
Tier
1 and Tier
2.
Equation
J&El
5
calculates
the
effective
diffusion
coefficient
through
the
cracks
using
soil
parameters
representative of the
soil within
the
cracks;
as
these
parameters
cannot
be measured
directly,
the
default
values
in
Tier
I
apply.
17
Equations
J&E16
through
J&E18
calculate
site-specific
geotechnical
parameters.
J&E16
gives
the
total
porosity,
which
is
the
ratio of the
volume
of voids
to
the
volume
of soil
sample.
J&E17
gives
the
water-filled
soil porosity,
which
is the
ratio
of
the
volume of water
to
the
volume
of
soil.
J&E18
gives the air-filled
soil porosity,
which
is a measure
of
the
total
porosity
minus the
water-filled
porosity.
Porosity
values
representative
of the soil
layer
at the
source
of
contamination
as
well
as each
soil layer
through
which contaminants
migrate are
needed to
calculate
the effective
diffusion
coefficient
(J&E1 1).
Additional
methods
for
determining
the
physical
soil
parameters
are presented
in
Section
74iAppendix
C,
Table
F.
It is possible
to
calculate
a Tier
2
soil
remediation
objective
more
stringent
than the
Tier
I
soil
remediation
objective
for
the
indoor
inhalation
pathway;
in
such
cases,
the
Tier
I
remediation
objective
applies.
This
practice
is consistent
with the
other
exposure
routes
in
TACO.
Subpart
H: Tier
2 Groundwater
Evaluation
Section
742.805(e)
requires
site evaluators
to
follow
Section 742.812
in
calculating
groundwater
remediation
objectives
for
the indoor
inhalation
exposure
route.
Under
Section
742.812,
site evaluators
follow
the J&E
equations
presented
in
Section
742.7
17,
only
equation
J&E7
is
used
instead of
equation
3&E5,
and
when
determining
the
attenuation
factor,
the capillary
fringe
must be
considered
one
of the
layers in
equation
J&E9a.
The
capillary
fringe is
the
zone immediately
above
the saturated
zone
where
capillary
attraction
causes
upward
movement
of
water
molecu.les
from
the
saturated
zone
into the
soil
above;
it contains
more
water
than
the
rest
of
the soil
above the
water table.
This
zone
is
distinct
in
that
it
has characteristics
of both
the vadose
and
saturated
zones.
Because
the
capillary
fringe
impacts
the migration
of
contaminants
from
the water
table, it
must be
considered
as a
separate
18
soil layer
when
developing
remediation
objectives
for
groundwater
and
a
default
thickness
of
17
cm must
be
used.
This value
comes from the
U.S. Soil Conservation
Service
soil texture
classification
table,
which is
also used by
U.S. EPA
for
determining
soil-dependent
properties
for
the J&E
model.
In
addition, the
default water-filled
soil
porosity of the capillary
fringe
is
assumed to
be 90
percent
of
the
total
porosity of
the soil that
comprises the
capillary
fringe.
The
thickness
of
the capillary fringe
and
its
water-filled soil porosity
cannot
be measured
accurately
in the field on a
site-specific
basis,
which
is why site-specific
values
are
not allowed.
Subpart
1:
Tier 3 Evaluation
Section 742.900(c)(1
0)
identifies the
use of
building
control technologies
—
different
from
those presented in Subpart
L
— as
a
situation
eligible
for
a Tier
3 evaluation.
Site
evaluators
wanting to perform
a Tier
3 evaluation for reasons
of
impractical
remediation
(Section
742.920)
or exposure
route
exclusion (Section
742.925)
for
the
indoor inhalation
pathway are
directed
to
follow
Section
742.935.
Under
Section
742.935, site evaluators
may
propose
to
use calculations
arid
modeling
to
establish remediation
objectives; use
soil
gas
data,
such as
sub-slab
sampling;
and use
building
control
technologies
different
from
those
presented
in
Subpart
L.
In
‘Section
742.93
5(a), the indoor
inhalation
pathway may be
excluded through
calculations
and
modeling
to account
for contaminant
transport
from soil,
groundwater
or soil
gas
into
a building. Unlike
Tiers 1
and 2,
the
calculation
of
Tier 3
remediation
objectives
for
the
indoor
inhalation
exposure route must
take into
account the
possible migration
of chemicals
caused
by
both
diffusion
and advection.
If
the
contamination
is more
than
five
feet
from
an
existing or
potential building
or man-made
pathway,
a value
of
zero for
the
volumetric
flow rate
of
soil gas into
the
enclosed space
(Q
01)
must
be used.
A
Q
value
of
zero
means that
the
19
controlling
mode
of
contaminant
transport is diffusion
and
not
advection.
If the
contamination is
within
five feet
of
an existing
or potential
building
or
manmade
pathway,
then
a
Q
value
of
83.33
cm
3
/sec
must be
used
in calculating
the attenuation
factor
(equation I&E8a),
unless
additional
site-specific
infoimation indicates
a
different
remediation
objective
is
reasonable
and
appropriate.
A
Q
0
assessment under Tier
3
is
a balancing
factor
to
make
sure these
alternative
evaluations
remain
health-protective.
In
Section
742.935(b),
site
evaluators
may
propose to
establish remediation
objectives
using
soil gas data in lieu
of
the
requirements
of
Section 742.227.
One such
difference
is the
use
of sub-slab samples
collected
directly
beneath a
building
foundation.
Section
742.227
applies
to
exterior
samples collected
near
the
building,
which
is
Illinois EPA’s
preferred
approach
as
it
is
the least
invasive. However,
because sub-slab
sampling
is an accepted
methodology
nationwide,
Illinois EPA
decided
to reference
it specifically under
Tier 3. This
section identifIes
what
information
a site
evaluator must
submit to Illinois
EPA to demonstrate
the
validity
of
alternative
soil
gas
data in
calculating indoor inhalation
remediatiort
objectives.
Section
742935(c)
must
be
used
when
site evaluators propose
a
mitigation
system
that
deviates
from the building
control
technology
requirements
presented
in Subpart
L.
This
section
identifies
what
information
a site evaluator
must submit
to
Illinois
EPA
to
demonstrate
the
effectiveness
of
art
alternative
building
control
technology
to
prevent
or
nii.tigate
indoor
inhalation
exposure risks.
Subpart
3:
Institutional Controls
Section 742.l000(a)(7)
requires
the use
of
institutional
controls whenever
rernediation
objectives
are
based on a
building control
technology. Section
742.1015(j)
prohibits
the use
of
a
groundwater
ordinance to
exclude
the
indoor
inhalation
exposure
route. As
described
previously,
20
this
is because
an
ordinance restricting
the source
of
drinking
water
would
not protect
the
enclosed
air space
of
a building
from
the
migration
of
contaminants
in the
groundwater.
The
other iostitutionai
controls available in
TACO
for land use restrictions
and engineered
barriers
may stiU be
used, though
Highway
Authority
Agreements
will likely
not
apply
to the
indoor
inhalation
exposure route.
Subpart
L:
Building
Control
Technoloaies
Building control
technologies are
designed to prevent
the
migration
of volatile
chemicals
into enclosed
spaces.
They
control
unacceptable
health risks due to
vapor
intrusion by
reducing
or
eliminating
the concentrations
in
the
indoor
air without
necessarily
reducing
the
residual
concentrations
in soil, groundwater,
or soil
gas.
The
objective
of these
measures is
to make
the
indoor
iriiialation
exposure
route
incomplete
by
preventing
the
migration
of chemicals
into
a
building.
Section
742.1200
establishes the
use
of
building
control
technologies
as
an
acceptable
final
coffective action and
requires that the site
evaluator also
comply
with the
provisions
of
Subpart
Jregarding
institutional controls.
This Section
allows
for
no further
remediation
determinations
to be made on
building control
technologies for
buildings not
yet
constructed,
provided
that the approved
technology
is
in
place
and
operational
before
human
occupancy.
Site
owners and
operators
are required to
maintain building
control
technologies;
specific
maintenance
duties will be
contained in the institutional
control,
In
the
event that the
system
shuts down,
site
owners and operators
are required
to
notify
building occupants
and
workers
and
implement protective
measures to prevent
exposure to the
contaminants
of
concern.
System
inoperability
may
occur
during
routine maintenance
or
power
failures.
Contingency
measures
will
be contained
in the institutional
control;
this practice
is
consistent with
provisions
in place
21
for
engineered
barriers
used
by the other
exposure
routes.
Lastly,
this
Section
states
that
the
no
further
remediation
determination
may
be
voided
if
the building
control
technology
is
not
maintained
as
stipulated
in the
institutional
control.
Section
742.1205
lists the
information
to be submitted
in
a
proposal
to
use
any
of
the
three
mitigation
systems
under Subpart
L.
Section
742.1210
defines
the specific
requirements
for three
common
mitigation
systems:
sub—slab
depressurization,
sub-membrane
depressurization,
and
membrane
barrier systems.
This
Section
specifically
prohibits
natural
attenuation,
access
controls
and point
of use
treatment
from
use as
building
control
technologies.
Also, building
control
technologies
cannot
be used
as
part
of
a
Tier
1 evaluation.
Sub-slab
depressurization
is
an
active
venting
system
that
draws
contaminated
soil gas
from
beneath
the building
and expels
it
to the
atmosphere.
Sub-slab
depressurization
systems
can
be
used
for existing
and new
buildings.
Sub-membrane
depressurization is similar
to
the
sub-slab
depressurization
system,
but
used
for existing
buildings
with
crawl
spaces.
Membrane
barrier
systems
are
used for new
building
construction
and serve
to
physically
block
the
entry of
contaminants
into
interior air
space.
This
concludes
my
testimony.
Errata Sheet
Number
1
Illinois EPA
would
like to
remove
Section
742.12
lO(c)(4)
from
the
proposed
rules.
This
section
contains
the
building
control
technology
requirements
for
a barrier made
of
geologic
materials.
This
language
was
added early
on in
the
rulemaking
development
when it
made
sense
to offer
a
barrier
parallel
to
the engineered
barriers
available
for
the
ingestion
and
outdoor
22
inhalation
exposure
routes.
Instead of
specifying
a
depth requirement
as for
the other
two
pathways
(three
and 10
feet, respectively),
Illinois
EPA
stated
that
the
depth
was to
be
determined
using
either
Tier 2
or Tier
3.
We have
since
tested the
practicality
of
a
geologic
barrier
for the
indoor
inhalation
exposure
route by
calculating
the
depth
needed
to
meet
the
requirements
of
742.121 0(c)(4)
using
data
from
an
actual
site. It
turns out the
J&E
model
can’t answer
the
question.
Illinois
EPA
knew
that depth
to
source
is
one of
the
least sensitive
parameters
in determining
remediation
objectives,
but
didn’t
fully appreciate
the
implications.
Because
the model
assumes
an
infinite
source
of
contamination
without
degradation,
no
depth
of geologic
materials
would
be
sufficient
to
exclude
the
pathway.
Site evaluators
have
reasonable,
cost-effective
options for
exclusion
using
the
remaining
three ECTs,
and
should
a
site
evaluator
want to
propose
a
geologic
materials
barrier
using
an
alternative
methodology
for determining
a
depth
protective
of
building
occupants,
that
option
is
available
under
Section
742.935(c).
23
EXHIBIT
Instances
of Vapor
Intrusion
Risk at Sites
in Illinois
Below
are
seven
case studies detailing
remedial
efforts
at contaminated sites
in
Illinois.
These case
studies serve two purposes.
First,
they are meant
to give the
reader
an
overview of
the variety
of
sites
and
cleanup programs
affected
by
vapor
intrusion
risks.
Second, and
more importantly,
these
case
studies illustrate
the need for
consistent
and
comprehensive
regulations
for evaluating
and
managing the indoor
inhalation
exposure
route.
For
example,
the Peoples
Gas
site and
Bell
Fuel site
demonstrate
how
the
lack
of
Tier 1
remediation
objectives
and a
defined
sampling protocol
for the indoor
inhalation
exposure
route
may cause unnecessary
work that
is costly and intrusive
and lead
to
site
evaluation
results
that
may
be unreliable.
Without
regulations
in
place, Illinois
EPA, site owners,
environmental
cleanup
professionals and
future
property
users
experience
problems
in interpreting site
data
and
uncertainty as to remediation
goals.
Acme Solvents/Rockford:
Remedial
Project
Management
Section; State
SItes
Unit
The
Acme Solvents Site
is
located in an
industrial
area
southeast of
downtown
Rockford,
on
the
southwest
corner
of the
intersection
of
15
th
Street
and
20
th
Avenue.
According
to Illinois EPA
records,
Acme
Solvents
began operation
as a
solvent
reclaimer
in 1955.
Illinois EPA
inspections
from
1980
to
1983
noted
numerous
violations
of
RCRA
storage
and
disposal regulations,
including
spills
and
poor
housekeeping.
In
1984
a
Civil
Complaint
was filed against
Acme for violations
of the
Hazardous
Materials
Transporting
Act.
Acme
Solvent
Reclaiming,
Inc.
ceased
operation
in 1986.
In the late
1980’s Illinois EPA
conducted
an investigation
of
the
Acme
Solvent Site
and
determined
that
significant
concentrations
of chlorinated solvents,
BETX
and
other
volatile
chemicals
were present
in the
soil
and
groundwater.
Further
investigation
by
the Responsible
Parties
determined
that soil impacts
extend
off-site
to
one
adjacent
property
and groundwater
impacts
extend
to a
number
of
off-site properties.
Soil and
groundwater
concentrations exceeded
the
draft
TACO
Tier
1
soil
and
groundwater
indoor inhalation
remediation
objectives. As a
result,
in
2008
the
Responsible
Parties
collected
soil
gas
samples
at
three
adjacent
off-site
properties.
A
number
of volatile
chemicals
were
detected
in
the
soil gas samples
at concentrations
exceeding
the draft TACO Tier
1
indoor inhalation
objectives.
Based
on
the
results
of
the soil
gas
samples,
the
Responsible
Parties
completed
a nsk assessment
and
determined
that the indoor
inhalation
risk at each of
the
adjacent
properties has
an
incremental
lifetime
cancer
risk less
than
lx
6
10 and
a
hazard quotient
less than
1.
To
further
reduce
risks,
the Responsible
Parties
are
proposing
soil
vapor
extraction
and air
spa
rglng at
the Acme Solvents
Site.
1
9-18-08
Devon
Bank/Wheeling:
Remedial Project
Management
Section, Site
Remedlation
Progra
rn
The Devon
Bank Site,
located in
Wheeling, Illinois, is
part of
a
larger
remediation
site
that
includes several properties
owned
by
Interstate
Brand Corporation.
This
particular
property was
formerly
occupied
by a
drycleaner, which
contaminated the
area
with
volatile chemicals,
Perchiorocthyiene
(PCE),
a
chemical
commonly used by
the
dry
cleaning industry, was
detected
at
levels
exceeding
TACO Tier
1
soil remediation
objectives. Trichloroethylene
(TCE),
commonly
used as
a metal
degreaser,
was also
detected
at levels exceeding
TACO
Tier 1
soil
remediation
objectives.
During
the remedial
process,
in-situ
chemical oxidation
was used to lower
concentrations of
PCE
to
an
acceptable remediation
level
under
TACO.
However,
concentrations
left
in the
soils
at
the Devon
Rank Site posed
a
risk
of
vapor intrusion.
To
address this concern,
in
2008
Devon
Rank Installed
a
vapor barrier
membrane
beneath
the foundation
slab to exclude
the
potential
for
chemicals to
migrate into
the
building.
People
Gas/Chicago: Remedial
Project
Management
Section,
Site
Remedlation
Program
People’s Gas
Site, formerly known
as 31
Street
Gas
Distribution
Center, served
as
a
storage and
distribution
facility for
manufactured
gas
between
1887
and
1934.
Two
gas
holders
and
various gas distribution
piping
and equipment
were on the site.
After
closure
the
property
was transferred
to
the Chicago
Housing
Authority
and
eventually
developed
into
Bridgeport
Homes,
which
consists of 13
two-story brick
buildings, each
containing several
residential units,
and
a
two-story
community
building. The
buildings
are slab
on grade with
no
basements.
Previous soil and
soil
gas samples showed
contamination
from benzene,
naphthalene,
semi-volatiles,
and
metals,
In 2004, indoor
and outdoor air
samples were
taken from
the
first
and
second
floors of
five
occupied
and eleven
unoccupied units
in the
housing
complex. Illinois
EPA coordinated
with the
Illinois Department of
Public Health
because
air samples were
taken inside
the
residences.
The results
of
indoor
air sampling found
elevated
naphthalene
in
two
unoccupied
units
(A
and B). Construction
materials
were
stored
in
unit
A
and unit
B, which
had
recently
undergone
renovation.
In
both
units
naphthalene
levels
were
higher on the second
floor
than
on
the
first;
however
the
Illinois EPA
and the Illinois
Department of Public
Health concluded
that
contamination
levels did
not pose a
threat
to
human
health,
and
were
probably
not
due
to
vapor
Intrusion.
Chanute Air
Force Base/Rantoul:
Federal Site
Remediation
Section,
Department of
Defense Program
2
9-18-08
The former
Chanute
Air
Force
Base occupies
nearly 2100
acres
in
Rantoul.
The
base
opened in
1917
and conducted
military
flight
operations
until
1971.
From 1971
until
all
military
operations ceased
in
1993,
Chanute
served
as a non-flying
training
base.
During
its
years of
operation,
hazardous
materials
were
used
at Chanute,
such as fuels
and
chlorinated
solvents.
Eighteen
structures
on
the former
base were evaluated
for vapor
intrusion,
but
two
buildings stand out as
particularly
contaminated. Building
343 served
as a
laundromat
and
has
a
history
of
trichioroethene
(TCE)
and
PCE
spills.
BuIlding
995
was ajet
engine
test cell;
TCE
and
vinyl chloride
are
the
primary
contaminants
at
this
location.
Vapor
intrusion
investigations
were
performed
at
the
base
during remedial
investigations
conducted
under
CERCLA.
The
Air
Force
conducted
sub-slab
soil gas
sampling
at
buildings within 100
feet of volatile
chemical-Impacted
groundwater.
These
measurements
exceeded
U.S. EPA
screening values
corresponding
to
target
carcinogenic
risk levels
of
10 for indoor air
inhalation. The
risk assessment
model used
by
the Air
Force indicates
that
remedial action or
institutional
controls are
needed
to
ensure
protection
of potential future
residents.
Southeast
Rockford/Rockford:
Federal
Sites
Remedlation
Section,
Superfund
Program
The Rockford Groundwater
Contamination
Superfund Site
contains
two contaminated
Areas —4 and
7—with vapor
intrusion
potential.
Area 4
is a mixed industrial/commercial
and residential
use
area. The
source
of
the
volatile
chemical
contamination
is located across
the street from
residences
to the
west
and
a
mobile home park
is
located
to the east (up
gradient). The
groundwater
plume
extends
down gradient under
the
houses. Soil
gas
samples
collected during
many
previous
phases
of
investigation
detected volatile
chemicals
on
the
western
edge of
the
mobile home
park.
Initial
indoor
air
samples
were
collected
in
1993.
1,1,1-TCA
and
TCE
were detected
but at concentrations
below
heafth-based
screening
levels
available
at
the
time. A second
round
of
sampling was
done
in 2003
using
four
houses in the
affected
area
and
a background
house. The houses
were
sampled indoors
and
outdoors, and
soil
gas
samples
were also
taken.
A groundwater
sample
was
taken
from
a
well
that
is
down
gradient/side
gradient
and
closest
to the
plume.
Risks to residents
were
estimated
from
the measured
indoor air samples
and modeled
indoor
air
concentrations
from
the soil
gas.
No
data
were
currently available
that
adequately
characterized
shallow
groundwater In the
vicinity
of
the
residences; risks
from
groundwater
were
not assessed.
The
results of
the indoor
and outdoor
air
samples,
as
well as the
soil gas
samples,
showed
signs of vapor intrusion
in
some
areas,
In
one case
due to an
improperly sealed
well
pit which
provided a
migration
pathway
for
vapors
in
the
groundwater
into
the
home.
That well has
since
been sealed.
3
9-18-08
Area
7 contains a park
owned
by
the
Rockford
Park
District
and is
bordered
by a
subdivision
on
the
east
and
west.
The
cause
for
contamination at
the
site
is
a
former
open dump.
The groundwater,
which
extends
underthe
subdivision, is
contaminated
with
volatile
chemicals.
Initial
air samples
taken
in
1993
detected volatile
chemicals
at
concentrations
below
heafth-based
screening
levels available at
that
time.
The
results
of
this sampling
did not correlate to
the groundwater
contamination
and
there
were no
obvious
signs
of vapor
intrusion.
In
July
and
August
of
2003,
a second
round
of
sampling
was conducted.
Five
houses
in the
affected
area
and
a
background
house, used as
a
control, were
air sampled indoors
and
outdoors; soil gas samples
were collected,
and
groundwater
was
tested.
The
results
were
mixed; chemicals
were
found
but
not
deemed
hazardous
to
human
health.
Premcor/Hartford:
RCRA
Corrective Action
Premcor
Refinery, the largest
independent
petroleum
refiner
in
North
America,
Is
located
on
400 acres in the
village
of
Hartford,
Madison
County,
Illinois.
Since
the
1940’s
the
site
has operated
under
various owners
as
a
petroleum
refinery.
Bordering
Premcor are
two
other
refinery sites. Amoco
operated
from
1980-81,
and
ConocoPhillips
is currently in
operation.
In
the 1970’s and 1980’s
residents
in the
Hartford area experienced
gas odors in
their
basements,
while some
residents
experienced
fires
and explosions.
The matter
was
referred
to the Illinois
Attorney
General who
urged
all
three
operators
to
study
gasoline
composition.
Illinois
EPA
conducted
fingerprinting
and geo/hydrology
studies which
found
that Clark (now
Premcor)
was the
predominant
source
of the
gasoline
under
north Hartford.
Illinois
EPA
and
the
Attorney
General’s
Office negotiated
with Clark/Premcor
in the
1970’s
and
again
in the 1990’s
to
install recovery
systems
to
mitigate
the effects
of
the
leaks. The
first
system,
recovery wells,
captured 1.16 million
gallons of
gasoline. The
second
system,
vapor recovery,
has captured
the equivalent
of
1.8
million
gallons
of
gasoline, and still
operates;
however, Premcor
no longer
operates
the recovery
wells.
Since
the
implementation
of
these
recovery systems,
citizens
have
continued
to
complain about
gas vapors.
There
are
several
environmental and human
health
concerns
due
to
contamination.
The
groundwater
under Hartford
may contain
several
million gallons of
hydrocarbons,
and
in May
2002
the
Illinois
EPA
found
explosive
levels of vapors
in
homes
along a
corridor of Hartford.
The Illinois EPA also
found,
in 2002,
elevated
levels
of
benzene
in
many
homes, and determined
that
residential vapor intrusion
was
a
public health
hazard.
In May
2003, Illinois EPA requested
that
U.S.
EPA, Region 5
conduct
a
time
critical
removal assessment,
assess
current
site
conditions,
and determine
if
possible
removal
actions were
warranted
at
the
North Hartford
Premcor
Site,
US.
EPA
has
assumed
primary
responsibility
for addressing
the problems
at the
Hartford
Site
since
the
4
9-18-08
summer
of
2003.
The
recent
court decision
in
United States
v.Apex
No.
05-CV-242-DRI-1
(July 28,
200€)
details
the court’s
findings
with regards
to
vapor
intrusion
issues
and
the
response actions
used
to address
them.
Bell
Fuels/Chicago: Leaking
Underground
Storage Tank Section
Bell
Fuels
Site
is a
former
fuel distribution
center
located
on
a
corner lot in
Chicago.
The
site
is situated
between
a
residential
neighborhood,
and
a
rail
yard.
In
2000, a leaking underground
storage
tank
released
fuel into the subsurface
soil.
Groundwater
and
soil
gas samples
were
collected
in
May
2007 and
analyzed
for
chemicals
of concern. No
volatile
chemicals were detected
above
the
reporting
limit
in
the groundwater.
The soil
gas test results were
compared to
the U.S. EPA
Target
Shallow Soil
Gas
Concentrations.
Some of
the results,
as well
as some
of the
reporting
limits
were greater
than
the risk
level given
by the
U.S. EPA.
Sub-slab samples
were collected
at two locations
in
each of
three
potentially
impacted
houses.
Only one chemical
of
concern
was detected
from each sample,
but in
concentrations less
than the U.S.
EPA
Target
Shallow Soil
Gas
Concentrations.
Indoor
air
samples were
also taken
from
two locations,
the
basement
and
first
floor,
in
each of
the
three houses.
Results
from
those samples revealed
at
least
one
chemical
of
concern
from
each sample. However,
there
may
have been
problems
with the
sampling
method
which
could
have
produced
false
positives.
For example,
in
a house
where elevated
levels of
benzene
were
found,
the resident
had smoked
a
cigarette
Just
as
the
samplers
arrived.
Furthermore,
the indoor
air sampling protocol
was not included
with
the
report.
5
BEFORE
THE
ILLINOIS
POLLUTION
CONTROL
BOARD
IN THE
MATTER
OF:
)
)
PROPOSED
AMENDMENTS
TO
)
TIERED
APPROACH
TO
CORRECTIVE
)
R09-9
ACTION OBJECTIVES
)
(Rulemaking-Land)
(35 III.
Adm. Code
742)
)
PRE-FILED
TESTIMONY
OF
TRACEY
BURLEY
Oualiffcations
My
name
is Tracey
Hurley.
I am an Environmental
Toxicologist
with
the
Toxicity
Assessment
Unit at
the
Illinois
Environmental
Protection
Agency
(“Illinois
EPA”).
I
have
been
with
the
Illinois EPA
for twenty
years.
I have
been
a
member
of the
Illinois
EPA’s
workgroups
that developed
the
original
35 111.
Adm.
Code
Part 742 rule,
Tiered
Approach
to Corrective
Action
Objectives
(“TACO”,
R97-14)
and subsequent
amendments.
I was a
member
of the
Agency’s
workgroup
that
developed
the
onginal
35
Ill.
Adm. Code
Part
620
rule,
Groundwater
Quality
Standards
(PCB
R89-14).
I
have a Bachelor
of
Science
degree
in
Biology
and a
Master
of
Public
Health
degree.
Testimonial
Statement
I
will
be
testifying
in
support
of
the proposed
amendments
to
35 Iii.
Adm.
Code
742:
Tiered
Approach
to
Corrective
Action
Objectives.
I
will
present an
overview
of the
updates to the
tables
in
Appendices
A,
B,
and
C
and
Errata
Sheet
1.
There
are four
main explanations
for the revisions
to the tables:
changes
in the
toxicity
values,
changes
in the
physical
and
chemical
parameters,
addition
of chemicals
1
as
a
result
of
their
inclusion
in
the proposed
Groundwater
Quality Standards
(35
Ill.
Adm.
Code
620,
R08-l 8), and
addition
of
the
indoor
Inhalation
exposure
pathway.
Rick
Cobb,
illinois
EPA,
provided
testimony
on
the addition
of chemicals
to the
proposed
Groundwater
Quality
Standards during
the Part
620 hearings
(R08-l
8). Gary
King,
illinois
EPA, will provide
more
detailed
testimony
on
the Indoor
Inhalation
exposure
pathway.
I
will
first describe
the reasons for
the changes in
the
toxicity
values
and
physical and chemical
parameters
in
more
detail
before
I discuss
the
changes to
the
tables.
In the
process of calculating
Tier
1 Remediation
Objectives
for the
indoor
inhalation
route,
illinois
EPA
realized
that
physical
and
chemical
parameter
values and
toxicity
values
had changed
for several
of the chemicals.
We
decided
against a
partial
update
to TACO using
corrected values
to
calculate remediation
objectives
only for
the
indoor inhalation route
because
this
would
have
resulted
in
the volatile
chemicals
having
remediation
objectives
for
the indoor
inhalation route
calculated
with revised values
while
the ingestion
and
outdoor
inhalation remediation
objectives
would
have
been
calculated
with
the old
values.
Therefore,
we decided
to revise all
of the Tier
1
soil
and
groundwater
remediation
objectives
in
the
same rulemaking.
The
revised
physical
and
chemical parameter
values are
the result
of
updates in the
sources the Illinois
EPA
uses
for this
information.
These
sources
include the
following online
databases:
USEPA’S
Superfund
Chemical Data
Matrix
(LSCDM),
CHEFATE,
PhysProp,
USEPAs
Waler9
software
for
diffusivity
values,
and
Handbook
of
Environmental
Degradation
Rates
by
PH.
Howard
(1991) for
first order degradation
constant
values.
The
SCDM database
and
Water
software
were used
by USEPA
in
developing
the
Soil
Screening
Levels
(“SSL”),
2
• The CHEMFATE
and PhysProp
databases
are
the
original sources
for some
of the
information
in
the SCDM
database. Howard
(1991)
also was
used
by USEPA
in
developing
the
Soil
Screening Levels.
On
December
5,
2003,
USEPA
issued a
memorandum
(OSWBR
Directive
9285.7-53)
from Michael B.
Cook, Director
of the
Office
of Superfund
Rernediation
and
Technology Information,
to the Superfund
National
Policy
Managers,
Regions
1-10, on
Human
Health
Toxicity
Values
in
Superfiind Risk
Assessments.
As
a result,
several
of
the
toxicity values changed
and some new
values
were
added.
As
discussed by
Tom
Hornshaw
during
the
Part
620
hearings
(R08-18),
this
memo revised
the hierarchy
for
selecting
human
health
toxicity
values
that
had
been
used
since
the
issuance
of
the
original
hierarchy
in
the
1989 Risk Assessment
Guidance
for
Superfund
(“RAGS”).
The
RAGS
hierarchy,
which
has
also been
used by
the
Toxicity
Assessment
Unit
in
developing
human health
toxicity
values,
was to first
use values from
EPA’s Integrated
Risk
Information
System
(“IRIS”)
database,
if available,
or else
values from
the
most
recent Health
Effects
Assessment Summary
Tables
(“HEAST”).
If no
toxicity
value
was
available
from
these
sources,
then
values could be
derived
from
literature
sources
or
a
request
could
be
made to EPA’s
National Center
for
Environmental
Assessment
(“NCEA”)
for provisional
toxicity
values.
The
revised
hierarchy still
specifies the
iRIS database
as the
first
option for
toxicity
values, but
now
includes second
and third
tiers
of
data
sources.
The
second
tier
is a
recently introduced
database,
EPA’s
Provisional
Peer Reviewed
Toxicity
Values
(“PPRTVs”),
available
from NCEA.
The
third
tier, Other Toxicity
Values, includes
three
named sources
but
could
also
include other
sources
as
appropriate. The
three named
3
sources
are
the
Agency
for
Toxic
Substances
and
Disease
Registry’s
(“ATSDR”)
Minimal
Risk
Levels
(“MRLs”),
developed
for ATSDR
risk
assessments;
California
EPA’s
toxicity
values,
developed
to
support
various
rules
and programs;
and
EPA’s
HEAST,
which
was
last
updated
in
1997.
The
Toxicity
Assessment
Unit
has
adopted
this hierarchy,
with
some minor
revisions,
as
the
basis
for determining the
toxicity
values
for
its activities.
As
we
began
using the
new
hierarchy,
we
became
aware
of
some
minor
issues
that
ultimately
lead
to
certain
revisions
of
the hierarchy.
Three
issues
that
resulted
in
a minor
revision
are:
PPRTVs
are
retired
by
EPA
after a
certain
period
of
time,
leading
us to question
what
should
be the
role
of
retired
values;
we
ultimately
decided
to continue
using
them
instead
of
going
to
tier three.
•
EPA
does
not provide
guidance
on
which
value
to
use
if
more
than
one
value
is
available
from
the three
named
sources
in tier
three;
we
ultimately
decided
to use
the
lowest
of
the
tier
three
values
available
in such
cases
•
IRIS
does not
contain
values
for subchromc
exposures,
only
values
for
chronic
exposures,
so there
is
essentially
no
first
tier
for shorter-duration
exposures;
however,
some
chronic
IRiS
values
use
an
Uncertainty
Factor
to
extrapolate
to
chronic
exposures
from
a
study
of subchronic
duration,
and
we
have
used
the
IRIS
value
with
this Uncertainty Factor
removed
as the
first
tier
when
available.
The
Toxicity
Assessment
Unit
has
used this
new
hierarchy
to
re-evaluate
the soil
and
groundwater
objectives
for
all the
chemicals
currently
included
in
Part
742
(“TACO”),
other
than
those
groundwater
objectives
that
are
based on
a
Maximum
Contaminant
Level
from the
Safe Drinking
Waler
Act (which
would
require
a
change
at
4
the federal
level).
The
OSWER Directive
9285.7-53
has been
added to the
Incorporations
by
Reference,
Section
742.2
10. The reference
to
IRIS
has been
removed
from
Section
742.705(d)(2)
and the
OSWER
Directive
9285.7-53 added
in
its
place.
Appendix
A
Table
A
has
an
added
column
for
the
Soil
Saturation
Concentration
(“C”)
values
for
the
Soil Component
of the Groundwater
Ingestion Exposure
Route.
In
the
process
of
updating
the tables,
we
realized
that
each
chemical actually
has two different
C
values,
one
for the
Outdoor
Inhalation Exposure
Route
and
one
for the
Soil
Component
of the
Groundwater Ingestion
Exposure
Route,
These
exposure routes assume
different
default
organic
carbon content
of
soil
(“foc”) values
as
listed in
Appendix
C,
Table
B, The
Soil
Component
of
the
Groundwater Ingestion
Exposure Route
uses an
foc value
of
0M02 gig
because
it is
modeling
a
contaminant
that is moving
into
deeper
soils
with
a
lower
organic
carbon
content.
The
Outdoor Inhalation
Exposure Route
is
modeling
a
contaminant
that is moving
through surface
soils with
a
higher
organic
carbon content
of
0.006
gig.
The
C
values
listed
in
Appendix
A,
Table
A of the 2007
version
of TACO
are actually
for
the
Outdoor Inhalation
Exposure
Route
only.
It was
an oversight
that
C
values
for
the
Soil Component
of
the
Groundwater
Jngestion
Exposure
Route were
not
included
also.
The C values
listed in
Appendix
A, Table
A
have
been
calculated with the
updated
Solubility, Organic
Carbon Partition
Coefficient
(“K<,”), and
Dimensionless
Henry’s
Law Constant
(“H”)
properties of the chemicals.
The
C
values were
calculated
using equations
S
19 and S29 in Appendix
C,
Table
A.
The
physical
and
5
chemical
properties
used
in
the
equations
are
listed
in
Appendix
C,
Table
E. Three
footnotes
have been added.
Footnote “a”
specifies
that
the C
values
were
calculated
using an
foc of 0.006
gIg
and
a
system
temperature
of
25°C. The
values with
a “b”
footnote
were
calculated using
an
foc of
0.002
and a system
temperature
of
25°C.
Footnote
“c”
specifies
that
the
Csat
was
calculated
at a pH
of 6.8. If
a
site’s soil
pH is
a
value
other
than 6.8,
then a
site-specific
C
5
should
be
calculated
using
equations
S19
and
S29 and
the
pH-specific
K
values
listed
in
Appendix
C,
Table
I.
The
K
values
for
ionizing organic
chemicals
will
vary
with
pH.
The footnotes
are
new,
but the
practices
are
not.
Tables
E
and
F
have
been
updated with
fourteen
new
chemicals.
These are
the
same chemicals
that
have
been added
to
the proposed
Groundwater
Quality
Standards
(35
Ill.
Adm. Code
620,
R08-18).
The
target
organs
have
been updated
to
reflect
new
toxicity information.
Additionally,
the
tables
have
been
alphabetized
by
target
organ.
Table I
contains
six
new
chemicals.
Benzo(a)anthracene,
benzo(b)fluoranthene,
1,3
-dichloropropene,
and
gamma-HCH
should have
been
included
in
the
previous
versions
of
the
table,
but
were
inadvertently
omitted.
Because
of
the changes
to
35
111.
Adm.
Code 620,
we
were able
to
calculate
a groundwater
remediation
objective
based
on
the I0 risk
level
for
carbazole.
However,
it
does
not
have
an ADL
listed
in
USEPA’s
SW-846
methods
so it
appears
on
this table.
The
oral slope
factor,
and,
therefore,
the
1 in
1,000,000
cancer
risk concentration,
for 1
,2-dichloropropane
changed.
Bis(2-
ethylhexyl)phthalate
was
deleted
from the
table
because
its Class
I
groundwater
remediation
objective
is actually
equal
to
the
I
in
1,000,000
cancer
risk
concentration.
Vinyl
chloride
is listed
twice,
for residential
and non-residential,
because
the
slope
factor
6
is different
for
exposures
occurring
from
birth
and exposures
that
occur
during
adulthood.
The ADLs
for
chiordane
and
toxaphene
have been
deleted
to
reflect
changes
that
USEPA
has
made to
its
SW-846
methods.
The
Class
I
groundwater
remediation
objective
for
arsenic
has
been
changed
in accordance
with
35
III.
Mm. Code
620
(R08-l
8).
Table
J
is
a
new
table
containing
a
list
of
volatile
chemicals
thai
must
be
considered
for
the indoor
inhalation
route.
“Volatile
chemical”
is defmed
in 742.200
as
a
chemical
with
an
H’
value greater
than
1.9
x
10.2
or
a
vapor
pressure
greater than
0.1
Torr
(mm
Hg)
at 25°C
and elemental
mercury.
USEPA,
in
its “Draft
Guidance
for
Evaluating
the
Vapor
Intrusion to
Indoor
Air Pathway
from Groundwater
and
Soils”
(November
2002),
defmes
a volatile
chemical
as having
a Henry’s
Law
Constant
greater
tlan10
aim
m
3
Imol
(equivalent
to
an H’
value
of
4.1
x
10).
The existing
TACO
definition
for
volatile
organic compounds
is based on
SW-846
analytical
methods
or a
boiling point
less
than
200
°C
and
a
vapor
pressure
greater than
0.1
Torr
(mm
Hg)
at
25°C.
We
felt
that having
two
separate
defmitioris
for
volatile
chemicals,
one for the
indoor
inhalation
pathway using
USEPA’s
definition
and
one for the
other pathways,
would
be too
confusing.
In
addition,
USEPA’s
definition
includes
many
polynuclear
aromatic
hydrocarbons
(such
as
acenaphthene
and chrysene)
that
really
do
not volatilize
in
a
significant
amount. In
order
to
reconcile
the
two
definitions,
we looked
at
some
physical-chemical
properties
of
the
chemicals
and
whether
these
properties
determined
if
the
chemical
was
analyzed
by
an
SW-846
method
for
volatiles
or analyzed
as
a
semi-
volatile. The
physical-chemical
properties
we examined
included
vapor
pressure,
boiling
point,
H’, molecular
weight,
and
the
log
of
the
octanol-water
partition
coefficient
(“logP”).
logP
is
used to
calculate
K.
There did not
appear
to be
a
relationship
between
7
boiling
point,
molecular
weight,
and
logP to
the
analytical
method
for
the
chemical.
It
appears
that
chemicals
with
a
vapor
pressure
greater
than
0.1.
Torr
(mm Hg)
at 25°C
are
primarily
analyzed
as volatiles.
However,
this
criterion
does
not
classify
napbthalene
as
a
volatile.
We
wanted
to include
naphthalene
in
the
definition
of
a
volatile
chemical
because
it
can
be analyzed
either
as
a
volatile
chemical
(using
SW-846
method
8260)
or
as a
semi-volatile
(using
SW-846
method
8270).
Naphthalene
generally
is
considered
to
exhibit
characteristics
of both
a volatile
chemical
and a
semi-volatile
chemical
and
it
does
volatilize. Therefore,
following
USEPA’s
lead,
we
decided
to
include
H’ in
the
definition
of
volatile
chemical.
We
chose
a
value
for
H’ of
1.9
x
1
2
(Y
in
order
to
include
naphthalene
(H’ of 1.98
x
102).
Elemental
mercury
was
specifically
included
in
the
definition
of volatile
chemical
because
it
is
volatile
and
there
are
outdoor
inhalation
objectives
already
in
TACO.
Table
K
is
another
new
table.
It
lists
the Soil
Vapor
Saturation
Concentration
(“Cj
values
for
the
volatile
chemicals.
The
CV
values
have
been
calculated
using
equation
J&E6b
from
Appendix
C,
Table L,
the
default
parameters
listed
in
Appendix
C,
Table
M,
and
the
physical
and chemical
parameters
listed
in Appendix
C,
Table
B.
Table
L
also
is
a
new
table
and
it
lists the
C
values
for the
volatile
chemicals
for
the
indoor
inhalation
exposure
route.
These
Csat
values
have
been
calculated
using
an
foc
of
0.002
g/g
and a system
temperature
of
13°C.
Appendix
B
Tables
A
and
B
contain
many
revised
remediation
objectives
for
the
ingestion,
outdoor
inhalation, and the
soil
component
of
the
groundwater
ingestion
routes
of
exposure.
These
changes
have
been
made
because
of
revisions
to
the
toxicity
values,
8
pkysicallchemical properties,
and
the
proposed
amendments
to
35
Iii.
Adm.
Code
620
(R08-l
8).
Fourteen
chemicals
have
been
added
to
TACO
to
parallel
their
addition
to
35
Ill. Adm.
Code
620.
Footnotes
d,
f,
k (Table
B
only)
and r
were
revised
and
y
and z
were
added
to
clarify
the
basis
of
the
remediation
objectives.
Table
C
has been
revised
to
update
the
Class
I
Groundwater
Standard
for
arsenic.
For
Tables
C
and]),
the
lead
soil remediation
objective
at the
pH range
of
8.75
to
9.0 may
now
be used
up
to
a
pH
of
11.0.
These
pH
specific
soil
remediation
objectives
are
calculated
using
lcd
values.
We
have new
data with
a
valid
k
value
up to
pH
range
of
11.0.
This
is
applicable
only
to
lead
and footnote
“b”
has been
added
to denote
this.
In
Table
E the
Groundwater
Remediation
Objectives have
been
updated
to
reflect
clianges
in
the
toxicity
values
and
the
proposed
Groundwater
Quality
Standards.
Fourteen
new
chemicals
have
been added.
The
1
in 1,000,000
cancer
risk
level has
been
used
where
it is
greater
than
the
ADL for
carcinogens.
This is
in
accordance
with
changes
made
in 35 III.
Adm.
Code
620.Appendix
A.
The
corresponding
changes
have
been
footnoted.
Footnote
“e”
has
been
added
to
distinguish
between
the carcinogens
and
noncarcinogeriS.
Table
F
lists
the
GW
0
Concentrations
which
have
been
recalculated
to
reflect
changes
in
the toxicity
values
and
the
proposed
Groundwater
Quality
Standards.
Fourteen
new
chemicals
have
been
added and
the
changes
have
been
footnoted
accordingly.
Table
G
is
a
new
table.
In
it
are
listed
the
Indoor
Inhalation
Remediation
Objectives
for
soil,
groundwater,
and
soil
gas for
the
59
volatile
chemicals.
The
Remediation
Objectives
have
been
calculated
using
the
T&E equations
listed
in Appendix
9
C,
Table
L
and
the parameters
listed in
Appendix
C,
Table
M.
The
chemical-specific
values
for C
are
listed
in Appendix
A, Table
L,
and
physicallchemical parameters
are
listed
in
Appendix
C, Table
B.
If
the calculated
Tier
1
soil
remediation
objective
exceeds
the
C
value
of
the
chemical,
the
CsaL
value
is
shown
as
the rernediation
objective.
Similarly,
the solubility
limit
was
used for
the
groundwater
remediation
objective
and
the
was
used
for
the soil
gas remediation
objective.
Capping
the rernediation
objectives
in
this way
precludes
a
two-phase
system,
or
free product.
The models
used in
TACO
are
invalid
if
there
are two
phases.
Inhalation
toxicity
values
were not
available
for
nine
volatile
chemicals:
acetone,
bromodichioromethane, butanol,
chiorodibromomethane,
2-chiorophenol,
dalapon,
cis
l,2-dichloroethylene, n-nitrosodi-n-propylarnine,
and
1,1,2-trichloroethane.
Tier
1 soil
remediation
objectives
developed
for
these
chemicals
are
set
at
the soil
saturation
limit
calculated
using
the Tier
1
default
values.
Tier
I groundwater remediation
objectives
for
the indoor
inhalation
pathway
have
been
set at
the
solubility
limit
of
these
chemicals
in
water.
Illinois
EPA
decided
to
use
this
approach
rather
than
using the
oral
toxicity
values
because
it
is
not appropriate
to
do
so. The
chlorinated
solvents
are
metabolized
in
the
liver when
they
are
ingested
but
not
when
they
are inhaled.
This
means
that
the amount
of
chemical
andIor
form,
and
ultimately,
the toxicity,
of
the
chemical
that
is circulating
in
the body
is going
to
be
different
for
inhalation
and
ingestion
exposures.
Appendix
C
In
Tables
B and
I) the
source
of
the toxicity
values
has
been changed
from
IEPA
(IRISJHEAST)
to Jllinois
EPA. USEPA’s
latest
hierarchy
(OSWER
Directive
92857-53,
December
5,
2003)
for
Human
Health
Toxicity
Values
no
longer
lists only
IRIS
and
10
HEAST.
There are
three
tiers of
available
sources.
To
simplify
the source,
we
have
just
listed
Illinois
EFA.
Table B
lists
updated
Default
Physical
and
Chemical
Parameters.
The
14 new
chemicals
from
the
proposed
Groundwater
Quality
Standards
have
been
added.
All
values
are
now
expressed
in
scientWc
notation
for
ease
of
readability.
The
sources
for
the
physical
and
chemical
parameter
values
include
the
online
databases
USEPA’s
Superfund
Chemical
Data
Matnx
System,
CHEMFATE,
PhysProp,
USEPA’s
Water9
software
for
diffusivity
values,
and
Handbook
of
Environmental
Degradation
Rates
by
P.R. Howard
(1991)
for
first order
degradation
constant
values.
Table
F
has been
updated
to
include
the J&E
equations
to
the
“Method”
column
for
the parameters
of
total
soil
porosity,
air-filled
soil
porosity,
and
water-filled
soil
porosity.
Table
I
lists
the
organic
carbon
partition
coefficient
(“K’)
values
for
the
ionizing
organic
chemicals.
MCPP,
one
of the
chemicals
added
to
TACO
as
a
result
of
changes
to
the
620
Rules,
has
been
added
to
the
table.
2,4,5-TP
(Silvex)
has
been
deleted
from
the
table
because
its
K
does
not
change
over the
pH
range
of 4.5
of
9.0.
The
pH-specific
values
have
changed
as
a
result
of
chemical-specific
1C
values
and/or
pKa
(the
acid
dissociation
constant)
values.
Table
L
is
a
new
table
that includes
all of
the
equations
required
for
the
3&E
model.
Gary
King,
Illinois
EPA,
will
provide
testimony
on
the
modified
J&E
equations.
Table
M
includes
the
parameters
and
default
values
used
in
the
J&E
equations.
The
equations
from
Table
L
and
the
parameters
and
default
values
in Table
M
were
used
to
generate
the
Tier 1 Indoor
Inhalation
Remedialiori
Objectives
listed
in
Appendix
B)
Table
G.
Errata
Sheet
Number
1
This
part
of my
testimony
concerns
the
changes
made
to
the
appendices
in
Errata
Sheet
Number
1.
The
solubility
for
2-chiorophenol
in
Appendix
E,
Table
E was
incorrectly
listed
as
2.20E+05
mg/L.
It
should
be
2.20E+04
rnglL.
This
change
in the
solubility
results
in
different
C
values
in Appendix
A,
Table
A;
from
1.OOE+05
to
l
.OOE+04
mg/kg
and
from
7.OOE+04
to
7.IOE+03
mg/kg
for the
outdoor
inhalation
and the
soil
component
of
the groundwater ingestion
exposure
routes,
respectively.
The
value
for
the
indoor
inhalation
exposure
route
listed
in
Appendix
A,
Table
L has
changed
from
4.90E+04
to
4.90E+03
mg/kg.
The
remediation
objectives
that
are
Cai
based
need
to
be corrected
as
well.
The soil
remediation
objective
for the outdoor
inhalation
exposure
route
for
residential
properties
(which
is
capped
at
C)
listed
in Appendix
B, Table
A
has
changed
from
100,000
mg/kg
to
10,000
mg/lcg.
Similarly,
in
Appendix
B,
Table
B, the
soil
remediation
objectives
for
the
outdoor
inhalation
exposure
route
for
the
industriallcomrnercial and
construction
workers
have
changed
to
10,000
mg/kg,
capped
at
C.
The
soil
remediatiori
objective
for
the
ingestion
exposure
route
for
the
construction
worker
was
inadvertently
given
as
10,000
mg/kg.
It
should
be 1,600
mg/kg.
Also
affected
are
the remediation objectives
for the
indoor inhalation
exposure
route
listed
in
Appendix
B,
Table
G.
The soil
remediation
objectives
for
residential
and
industriailcommercial
properties
have
changed
from
49,000
mg/kg
to
4,900
mg/kg
based
on
the
C
for
indoor
inhalation
exposure
route.
The
groi.mdwater
remediation
objectives
for
residential
and
industrial/commercial
properties
have
changed
from
220,000
mg/L
to
12
22,000
mg/L
There are
a
couple
of
typographical
errors
on
Appendix
A, Table
A.
Dichiorodifluoromethane
is
misspelled
as dicblorofluommethane.
Its C
value
for
the
outdoor
inhalation exposure
route should
be
8.70E+02 mg/kg
not 8.70E+04
mg/kg.
The
C
value
for
vinyl chloride
for the outdoor
inhalation
exposure
route
should
be
2.60E+03
mg/kg
not
2.26E+03
mg/kg.
Also
in Appendix
A,
Table
A,
the
Ca
value
for the
soil component
of the
groundwater
ingestion
exposure route
is
not applicable
for
merciny
because the
groundwater
ingestion
remediation objectives
are based
on the
inorganic
form
of
mercury.
The
Cat
value
should be replaced
with
“NA”.
We
do not cap
the
remediation
objectives for the soil
component
of
the groundwater
ingestion
exposure route
at
the
values
for any
of the
inorganics
because
these chemicals are
analyzed
by a
different
analytical
method in
soil, the
TCU’
or
SPLP.
The
C
values
for mercury were
re
calculated
based on
the
following
information.
TACO uses
the oral
RID for
mercuric
chloride (inorganic
mercury)
as
the
basis for the
soil remediation
objectives
for the
ingestion
exposure
route.
The
groundwater
remediation
objectives are
based
on
mercuric
chloride,
also. The soil
remediation
objectives
for
the
indoor
and
outdoor
inhalation
exposure
routes
are
based on the
inhalation
RIO
for
elemental mercury.
Therefore,
the
C
values
for the outdoor
and indoor inhalation
exposure
routes
should be based on
elemental mercury
using the
K
and
other physical
and
chemical
values
from Appendix
C,
Table
B.
The
value
listed
in Appendix
C,
Table J is for
the divalent
form
of
mercury
(Hg+2) from USEPA’s
Soil
Screening
Guidance:
Technical
Background
Document
and should
not be used
for
calculating
the
C
values.
The C value
for the
13
outdoor inhalation
exposure route
listed
in
Appendix
A,
Table
A
will not change.
The
Cat
value
for
the
indoor inhalation
exposure
route listed
in Appendix
A,
Table
L
should
be changed
from 4.50E-01
mg/kg to l.05E+00
mg/kg. The
soil remediation
objectives
listed
in
Appendix
B,
Table
0 for the
indoor inhalation
exposure
route
for residential
and
industiiai/commercial
properties
should
be changed
from 0.45
mg/kg
to 1.05
mg/kg
because they
are capped
at the
C value. The
footnote N”
for
mercury
in
Appendix
B,
Table
0
should be changed
to specify
that
these remediation
objectives are for
the
elemental
form of
mercury.
This
is similar
to
footnote
“s”
in
Appendix B,
Tables
A
and
B.
The
statement
that mercury is
measured
in nig/L is
incorrect
and
should
be
removed
from footnote
“i”. The entry for
mercury
in
Appendix
C,
Table
I should
have
‘(+2)”
added to specify
that
the Kj value
is specific
to
this valence
state.
An
entry
was
inadvertently
omitted
from Appendix
A, Table
F.
1,3-
Dichloropropene
(cis + trans)
(inhalation
only>
should
be included
under the
category
of
Respiratory
System.
Incorrect
air
diffusivity
and
inhalation toxicity values
were used
in
the
calculations
for
2-butanone
(MEK).
Consequently,
the
soil
remediation
objectives
for
the
outdoor
inhalation
exposure
route listed
in Appendix
B,
Tables
A and B
for
all
receptors
are
incorrect.
The residential
and
industriallcornmercial
objectives should
be
25,000
mg/kg
(capped at
C)
and
the
construction worker
objective
should
be
730
mg/kg based
on non-cancer
effects. The
soil gas remediation
objectives
for
the indoor
inhalation
exposure route
listed
in
Appendix B,
Table
G
for
residential
and
industrial/commercial
properties should
be
capped at the
value
of 380,000 mg/rn
3.
The
rernediation
objectives
for
l,4-dichlorobenzene
were based
on cancer effects.
14
USEPA
and
California
EPA
classify
l.,4-dichlorobenzene
as
a
C or
possible
carcinogen.
TACO
defines a carcinogen
as class
A
or B carcinogen
only. Therefore,
the
rernediation
objectives
have
been recalculated
based
on non-cancer
effects.
In
Appendix
A,
Table
A,
the
soil
retnediation
objectives
for residential
properties
for
the
ingestion
exposure
route
should
be changed
from 120
mg/kg to
5,500 mg/kg and the
outdoor inhalation
exposure
route should be
changed
from 3.3 mg/kg
to
12,000 mg/kg. In Appendix
B, Table
B,
the
soil remediation
objectives
for
industriallcomrnercial
workers
for the
ingestion
exposure
route should
be changed
from 1,100
mg/kg to 140,000
mg/kg and the
outdoor inhalation
exposure route
should be
changed from
6.2 mg/kg to
20,000 mg/kg.
For
construction
workers, the outdoor
inhalation
exposure
route
should be
changed
from
8.8
mg/kg
to
320
mg/kg
The
ingestion
exposure
route objective
for
the
construction
worker remains
unchanged
because it
was based
on
non-cancer
effects.
The objectives
in
Appendix
B,
Table
G
for
the
indoor inhalation
exposure
route also have
changed,
The
soil
objectives
for
residential properties
and
industrial/commercial
properties
should
be
capped
at a
C
5
at
value
of 130
mg/kg. The
groundwater objective
for residential
properties
and
industriallcommercial
properties should
be capped
at
the water
solubility
value
of
79
mg/L.
The
soil gas
objective
for
residential
properties
and
industrial/commercial
properties
should be
capped
at
the
CV
t
value of 8,400
mg/rn
3.
The Values for
the
Soil Component
of
the
Groundwater
Ingestion Exposure
Route
for I
,3-dichloropropene in
Appendix B,
Tables
A and
B were calculated
with
the
old
values for
the
0
GW
bJ
(as
listed in
Appendix
B,
Table
F).
The values
for Class I
groundwater
should
be
changed from
0.003 mg/kg
to 0.0052
mg/kg. For
Class
ti
groundwater,
the
values should
be changed
from 0.015 mg/kg
to
0.026mg/kg.
-
15
The
Values
for
the
Soil
Component
of
the
Groundwater
Ingestion
Exposure
Route
listed in
Appendix
B,
Tables
A
and
B
for
methoxychlor
are
Csat
based
and should
be
4.5
mg/kg
for
both
Class I
and Class
II
groundwater.
This
is the
value
listed in
Appendix
A,
Table A
specific
to the
Soil
Component
of
the
Groundwater
Ingestion
Exposure
Route.
The
value
of
14
mg/kg
that
is
currently
in listed
in
Appendix
B,
Tables
A
and
B
is
the
C
1
for the
outdoor inhalation
exposure
route.
The
Values
for
the
Soil
Component
ofthe
Groundwater
Ingestion
Exposure
Route
for
2,4-dichlorophenol
for
Class
II
groundwater
listed
in Appendix
B,
Tables
A
and
B
should be
5
times
the Class
I
value
or
17
nag/Icg.
On
August
25,
2008,
USEPA
issued
a
revised
PPRTV for
cobalt.
This
PPRTV
contained
updated
oral
and
inhalation
toxicity values.
As
a
result,
the remediation
objectives
for
cobalt have
been
recalculated.
In Appendix
B, Table
A
the
remediation
objectives
for
residential
properties
for the
ingestion
exposure
route
should
be
changed
from
1,600
mg/kg to
23
mg/kg
and the inhalation
exposure
route
remediation
objectives
should be changed
from 1,100
mg/kg
to
360
mg/kg.
In
Appendix
B,
Table
B,
the
remediation
objectives
for
industrial
commercial
workers
for the ingestion
route should
be
changed
from
41,000
mg/kg
to 610 mg/kg
and the
inhalation
exposure
route
remediation
objectives
should
be changed
from
1,800
mg/kg
to
560 mg/kg.
Also
in
Appendix
B,
Table
B,
the
remediation
objectives
for construction
workers for
the
ingestion
route
should
be
changed
from
12,000 mg/kg
to
610 mg/kg.
The
parameters
of
solubility
and dimensionless
Henry’s
law constant
were
reversed
for
2,4,5-trichiorophenol
and
2,4,6-trichlorophenol
in Appendix
C,
Table
E
and
in the
calculations
for the
remediation
objectives.
These
two parameters
affect the
16
remediation
objectives
for
the
outdoor
inhalation
exposure
route
for
2,4,6-
trichlorophenol.
(2,4,5-Trichiorophenol
is not
affected because there
are
no
remediation
objectives
for
this chemical
for this
exposure
route.)
The
value listed
for
2,4,6-
trichlorophenol
for residential
properties
in Appendix
B,
Table A
should be changed
from 430
mg/kg
to 330
mg/kg. In Appendix
B,
Table B, the
value
listed
for
industriallcommercial
workers should
be
changed
from 820
mg/kg
to
630
mg/kg
and
the
value
for construction workers
should
be changed
from
1)200 mg/kg
to 890 mg/kg.
Also
in Appendix
B,
Table B, incorrect toxicity
values
were
used
to
calculate
the
remediation
objectives for construction
workers
for the ingestion
route. The remediation
objectives
should
be
changed from 200,000
mg/kg
to
61,000
mg/kg
for
2,4,5-trichlorophenol
and
from 11,000
mg/kg
to
2,000 mg/kg
for 2,4,6-trichlorophenol.
In Appendix B, Table
B, the bromofonn
value for
the
construction
worker
for
the
ingestion
mute of
exposure should have
a
“b” footnote
because
it
is based
on non-cancer
effects.
It
was incorrectly footnoted
with “e”.
An incorrect
value for
chloroform’s
remediation
objective
for
the
construction
worker
for
the
ingestion
route
is
listed
in
Appendix
B,
Table
B.
It
should
be
changed
from
2
,
000
b
mg/kg to
4,000e
mg/kg.
Dalapon
does not have
any
toxicity
values
available for the
inhalation
exposure
route.
As
a
general
practice,
illinois EPA uses
the
C
value
as the remediation
objective
if
the chemical
has a
melting point
less
than 30CC.
This
is
the
basis
of
the
value
that is
given
in
Appendix
B,
Table
B for the
construction worker,
120,000
mg/kg.
However,
for
workers,
we also
need
to look
at
whether
the
C based remediation
objective
is
protective.
This
practice was incorporated
into
the 2002
version of
TACO
for 1,1-
17
dichioroethylene
but was
removed
in the
2007
version
because
inhalation
toxicity
criteria
(“Reference
Concentration”) became
available
from USEPA.
It
was an oversight
that
this practice
was
not incorporated
into
these
proposed
TACO
rules.
Using the
Recommended Exposure
Limit
(“REL”)
established
by
National
Institute for
Occupational
Safety and
Health
of
6
3
mg/rn
to
calculate
a remediation
objective
for the
inhalation
exposure
route
yields
a value
of
11,000
mg/kg.
The
REL
based
remediation
objective
is lower than the
C based
remediation objective
and
should be
listed
in
Appendix
B,
Table
B.
We have
added
a
new
footnote
“aa”
to
explain
the basis
of this
objective.
The
remediation objective
for
the
ingestion
exposure
route
for the construction
worker
for
DDD
was
incorrectly
listed
as
360 mg/kg
in Appendix
B, Table B. It
should
be changed
to 520
mg/kg.
The
remediation objective
for
the
outdoor
inhalation exposure
route
for the
construction
worker for
l,2-dibromo-3-chloropropane
in Appendix
B, Table
B
has
an
incorrect
footnote.
The
footnote
should be
changed
to
“e” because
the
remediation
objective is based
on
cancer
effects.
The
Values
for
the Soil
Component
of
the
Groundwater
Ingestion Exposure
Route
for
di-n-butyl
phthalate
listed
in
Appendix
B, Table B should
be capped
at the
Cat
value
of
880
mg/kg,
as was
done
in Appendix B,
Table
A. The
value for
this chemical
is
lower
than
the
value
based
on the
Groundwater
Quality
Standard.
The
remediation
objective
for the construction
worker
for the
ingestion
exposure
route for
2,4-dimethyiphenol
is incorrect
in Appendix
B, Table B. It
should be
changed
to
10,000
mg/kg.
18
The
Values
for
the Soil
Component
of
the
Groundwater
Ingestion
Exposure
Route
for
2,6-dinitrotoluene
for Class
II
groundwater is
incorrect
in
Appendix
B, Table
B.
It
should
be
changed
to
0.0018
mg/kg.
The
remediation
objective
for
the industrial/conmierciai
worker
for
the ingestion
exposure
route
for
di-n-octyl
phthalate
in
Appendix
B,
Table
B
has
an
incorrect
footnote.
It should
have
a
“b”
footnote
because
it
is
based
on
non-cancer
effects.
The
Values
for
the
Soil Component
of the
Groundwater
Ingestion
Exposure
Route
for
hexachiorocyclopentadiene
for Class
U
groundwater
in
Appendix
B,
Table
B
should
be
capped
at
the
C
value
of
44 mglkg
for
the
soil
component
of
the
groundwater
ingestion
exposure
route.
The
value
that
is listed
is
the
Cat
value
for the
outdoor
inhalation
exposure
route.
There
is
a
typographical
enor
in the
remediation
objective
for
the construction
worker
for
the
ingestion
exposure
route
for
isopropylbenzene
in
Appendix
B, Table
B.
The
value
shouid
be
changed
from
82,00
mg/kg
to
82,000
mg/kg.
The
footnote
was
omitted
for the
rernediation
objective
for the
construction
worker
for
the
outdoor
inhalation
exposure
route for
2-methyiphenol
in Appendix
B,
Table
B.
The
value
should
have
a
“b”
footnote
because
it is
based
on
non-cancer
effects.
An
incorrect
footnote
is
given
for the
remediation
objective
for the
construction
worker
for
the ingestion
exposure
route
for
n-nitrosodiphenylamine
in
Appendix
B,
Table
B.
The footnote
should
be
changed
from “e”
to
“b” because
the
remediation
objective
is
based
on
non-cancer
effects.
The
remediation
objectives
for
the
outdoor
inhalation
exposure
route
for
n
nitrosodi-n-propylamine
listed
in
Appendix
B,
Table
B should
be
based
on cancer
effects
19
not
C.
The
value for industriailcommercial
workers
should
be
changed
from
1
,90()
mg/kg
to
022 mg/kg. The value
for
construction workers
should
be
changed
from
1,900
mg/kg
to
03
I mg&g.
An
incorrect
toxicity value
was used
to
calculate
the
remediation
objective
for
the
construction worker
for
the
ingestion
exposure route
for 2,4,5-TI’.
This
remediation
objective,
listed
in
Appendix B, Table
B,
should be changed
from 160,000
mg/kg
to
1,600 mg/kg.
USEPA issued
a
new
PPRTV
for
antimony
establishing
a
revised
subchronic
ingestion
toxicity
value.
As a
result, the
remediation
objective
for the construction
worker
for
the
ingestion exposure
route
in
Appendix B, Table
B
should
be
changed
from
41
mg/kg
to
82 mg/kg.
An
incorrect
footnote
is
given
for the
retnediation objective
for the
construction
worker
for
the
ingestion
exposure route
for chromium,
ion, bexavalent
in Appendix
B,
Table B.
The footnote should
be changed
from
“b”
to
“e”
because the remediation
objective
is
based on
cancer
effects.
This
concludes my testimony.
20
Indoor
Inhalation
Pathway
Slides
Presented
by
Dr.
Atul
Saihotra,
PtID.
Risk Assessment
and Management
Group
of
Gannett
Fleming,
Inc.
Houston,
Texas
The
purpose of
Dr. Salbotra’s
presentation
is
to
introduce the
indoor
inhalation
pathway
and explain
the
fate and transport
of
volatile
chemicals
into buildings.
He
is
not
an
expert on 35
111. Adm. Code
Part 742
or
on this
specific
proposed
amendment
(R09-
009),
but
a professional
risk assessor
whom Illinois
EPA consulted
in developing
and
thinking
through
various regulatory
options.
The
testimonies by Gary King
and Tracey Hurley
from
Illinois
EPA
will
address
everything
contained the
proposed
rule. Dr.
Saihotra’s role
is
to
lay
the
scientific
groundwork,
defining
concepts like attenuation
factor
and three
phase
equilibrium.
Dr.
Salhotra’s
information
is
presented in visual slides
because
in
this case
graphic
explanations
are
so
much
more
helpful
than
written
text.
Dr.
Saihoira
is
a
skilled
instructor; the
transcript of
his oral
presentation
from
the
Illinois Pollution
Control
Board’s
hearing
on this proposed amendment
will later serve
asan
additional
and
complementary
resource for interested
parties.
Subsurface
Soil
Volatilization Pathways
E1sfing [n1iiItion
Pthwy nndet TACO
Ambient
au’j
re*thing
zone
Gro.od
1
New Ixtha1aon
Pathway
Propo.ed
.urfce
Vdo
4tdeo c1Lb
Subsurface
—
Suhsurticv
W
I
Factors
that Affect
Migration
of Volatile
Chemicals
into
a Building
•
ic
ol
ihe
—
t.ilLfll
.J I
ttULI t
—
\
tIhlIIilTV
Il) iI1L
—
1)ilt
LtIIIJIIt(I1.L1(i
iiII1(I
• Iedii
IilFitIIt!h
‘
hh:h
L
‘t
icii,
in
ric
•
(tj;riLitv
—
\..td
‘L
/t ‘l1’
itititItn
iiiiiiii
ti
iti iiii
ii iituk
• (_haTtt_hIiItLs
oItach
iit.ditiiii
—
Ii
-
\\
.iei
c
—
\
t•lI•
i1ILti)ii
II
—
(
it:tii
L dIi’I1
_•tItICIil
Factors
that
Affect
Vapors
in
a Building
(continued...)
• (h;iIiLieri
si
lus
ol h’
bu
I
1
in
I I’vA(
S\sWm
Pisstt,e.\n
\ehuh1L!
tiLc
—
I
3
1S1’II1L’I1IS.
LI1\\ I
j-iu_.’.
slab OIi
—
I:ICJiOIs
—
IieIercnt
in)
r’
— (uIl.i1t
itil
,tjtiiiiI
IILIUIt.
IL’IeI(tIS
—
(ll\s
in huiIdii.s
lo;r
or
huscini’iii
walls
•
(1 ifll:illc
II&ktr
—
I t.Iujratur.
—
.—i
1111
S
)tIic.
IL’.5t.iiL’
Assessment
of
indoor
Inhalation
Pathway
•
‘\‘SC’IUCIl.l
I
ihi’
j.iv
is
c’IflIL’\
\LLI\
—
\‘1;mn\
IIc.1&Ns
IuI
ihe
nhltislon
ol
apnis
mo
;i
buiI(Iin.
Ihese
LtLnns
mmon
pttiul
.mnd
Imni’umuI
\II hmIiiv.
—
-k.lo[
1IL
im—pciIic
hut
lJNliI
hc
cisiI’
imicasumed.
1in.’
ot tin..
..hcnuciis ol concc’ln
mn.m
c
indoor
sources.
ic
.ttL&i jndLoi
air
(lt
nci
ieLssII,Iv
uip!
uhcurtmic
souic.
Necessary Conditions
for
Pathway
to
be
Complete
History
of Pathway
•
Radon
aLcumuhltion
(I
•
v1cihanc
iitiEiofl
tron
andflh1s
•
I
\VO sol
\L’nls
p1
times
in
(oloitdo
D()T
Maleriats
I L’S
Iahhv
!ctItie)d 1iI1c
Sae
indicated
indooi
air
impacts
( late
I
• I)iali
\
II()I
I
lItISii1
Utlidafluc
(
LPA.
2(H2)
• ;\SF
M
siand.ird
(
I:6OO_OX)
pnblishcd
in
2(1()X
Two
Processes
Cause
Movement
of
Vapors
•
I)
l’Ius
un
I’ri
na
rv
- \
1cituLit
\
ii
ii
1S
•
hfl
ihic
)
- Prssur
Di iftrenucs
0/
thc’.e.
(ud’rL’ctiulI
JIlaI•
01
‘,‘ar
lull
icdur.
He
,viII
l,rie/!r
I’riei
t’cIi
1fICL’SN.
Molecular Diffusion:
Qualitative
II
U
II
--
Q-
‘<
;.
‘<
<
c
it
I
_
I
Two
Methods
to
Evaluate Risks
to
Persons
for
Indoor
Inhalation
Pathway
• (ol
IL
i
lII
SZtIflflILN tI(I
inpm 10
iL ndoo!
I•
Lt
1IVLVIl(Ifl
1111S.
.1.
(_oII’ut
‘oiI Ifl(i
!!It)UI1d\VllCI
I
IS
dIl.I
LV
Ii
LIId1’
SLut
..iI(I
!I1utIL1(I’\
ItLI cur
NtlII
.!Is uL’IucdiltIuIu
obJLVII\
cS
till
LVi.Vc.IlIhlc
lli(It)Lil
JIr Ut)l1tLl1tIItII0l1’.
JOHNSON
& ETTINGER
MODEL
•
1—iii
pubh’hed
in
,cr
ic
Lii
ouriul
in
I
12
•
lSCi.I
[iv iiiiilv
and
• K cv
icchn
cii
LIliflLi)i
fliSSi(lfl
IlliLIL]
I)1i I)LILidLS
) ipe is
I
c I
r:t iniporl
n
tl
usc
,ui
nc
—
I)IpciNILc
•iducciic
iiiiIsj)uii!
ii
111111
IllIiIcliII
tiIlc_
iiilliieiirc
•
F
lUlL
sniicc
aelul
millie
(
I
11cc
InhUr
air
flhl\lfl
mild
and
tisk
c.iIciiinmn
• \liil1dlUIl,
iiliiIs
iiiil
Is1InINii’n
JOHNSON
& ETTINGER
MODEL
1
hc.. misL.h;i’cd
R()s Kir
indoor
inhal
lion
pah’
av arc
dcn cd
hiun
cqLI;IIiL)ns
Ii’iil_
Ille
lolloi
Illi_!
liiiV
Steps
I:
(
iiuUl,ttc
IaIi.!cI
or
acc
ahic
Illul uf
lii c*licdIlIL.It
loll
Stcp
2: (.mlculaIL’
altellaluil
lieu
Scj
3:
(
Ic
Lie
laicel
or
iccepiahie
soil e,u.
conecitlr:iliun
Step
-1:
(alctL.ie
arilel
r
acceptable
soil
and
oi eruiilld\\.icr
c4iIlcetl
I i-al
UII
l:acl
ol
ihe
sie’s
i’. hricl1
c’\plalileul
It
lle\t
sIids.
Step
3:
Calculate
Target
or
Acceptable
Soil
Gas
Concentration
Step
4:
Calculated
Target
or
Acceptable
Soil
and
Groundwater
Concentration
Estimation
of Tier
I ROs
Summary
of
Indoor Inhalation
Models
I flLIO&)F jnh1LL1
on
1nd
on:
I
Souic.
\Uj)Or CoI1C.1IntiO!l
2.
\‘l
ed
a
p.i a mLi
13u i id
i
n pn a
mdci’s
4.
I.n
lronnlcntai
Summary of
indoor inhalation
Pathway
• Indoor
inlijl
4
itinii
Nth\\
J\
IS
coiiueptuully simple
•
Hihu
;IY risk
depends on nuitierous
Inputs
•
Data
necessary to
e :iI nate
path way
can he
tol
leeted
and
aim lyzed in a
tnnelv and
cost-eheel
Re
\V\
•
(oneeptua lv
simple
methods can
he
used
to
make
the
patIiay
incomplete
•
l\’Iilwatzon
measures
(
lintltlinti (
ontrtd
Teelinolouies)
ought
to
he
e\
a
nated
as
a
part
ot
the site
concept
nat
mode I
STATE
OF
ILLINOIS
COUNTY
OF
SANGAMON
)
)
)
PROOF
OF SERVICE
I,
the undersigned,
on
oath
state
that
I have
served the
attached
Errata
Sheet
Number
1
and
the
Pre—filed
Testimony
of
Gary King,
Thomas
C.
Hornshaw,
Tracey
Hurley.
and
Arni
Saihotra upon
the
persons
to
whom
they
are
directed,
by
placing
a copy
of each
in an
envelope
addressed to:
Dorothy
Gunn,
Clerk
Illinois
Pollution
Control
Board
James
R.
Thompson
Center
100
W.
Randolph,
Suite
11-500
Chicago,
Illinois
60601
Matt
Dunn
Environmental
Bureau
Chief
Office of
the
Attorney
General
James
R.
Thompson
Center
100
W. Randolph,
12
th
Floor
Chicago,
Illinois
60601
Participants
on
the Service
List
Bill
Richardson
Chief
Legal
Counsel
illinois
Dept.
of
Natural
Resources
One
Natural
Resources
Way
Springfield,
Illinois 62702-1271
Richard
McGill
Hearing
Officer
Illinois
Pollution Control
Board
James R.
Thompson
Center
100W.
Randolph,
Suite 11-500
Chicago,
illinois 60601
and
mailing
them
(First
Class
Mail)
from
Springfield,
Illinois
on
November
12,
2008,
with
sufficient
postage
affixed
as
indicated
above.
/
/
t
BFIjgj
OFFIC
SEAL.
4
:
8
OEHNER
jyp
M’COMM1SSJØ,
EXPIRES
STATE
OF
H-S.2O
IWNOIS
t
U
(2
SUBSCRIBED
AND
SWORN
TO
BEFORE
ME
This
_J2L.
day of
November,
2008.
otary
Public
riuu1ig
oeivt
LASL....
rage
i
at
i
Party Name
Role
City & State
Phone/Fax
1021 North
Grand
Avenue
Springfield
217/782-
Illinois
Environmental Protection
Agency
5544
Interested Party
East
IL 62794-
PC) Box
19276
9276
217/782-
9807
Kimberly A. Gevlng, Assistant
Counsel
Annet
Godiksen, Legal Counsel
1021
North Grand
Avenue
Springfield
217/782-
IPA
PetItioner
East
IL
62794-
5544
P.O.
Box 19276
9276
217/782-
9807
Kimberly A.Gevi
ng,
Assistant
Counsel
217/523-
Hodae Dwver_Zemn
3150
Roland Avenue
Springfield
Complainant
Post
Office
Box
5776
IL
62705-
4900
5776
217/523-
4948
Katherine
ID.
I-lodge
Monica
T. Rios
Interested
Party
16650 South
Canal
IL
South
60473
Holland
Bob Mankowskl
Chemical
Industry
CounclLoL
Illinois
1400
East Touhy Avenue
DesPlai
n
es
Interested Party
Suite
100
IL 60019-
3338
LIsa
Frede
312/853-
elland& Sargis law Group.
LLP
19 South
LaSalle Street
Chicago
8701
Interested Party
Suite
1203
IL 60603
312/853-
8702
Mark
Robert Sargis
217/788—
Hanson
Enifneers
Inc.
Springfield
Interested Party
1525 South
Sixth Street
IL
62703-
2450
2886
217/788-
2503
Tracy Lundein
773/380-
Conestopa-Rovers
Interested
Party
& Associates
8615 West Bryn
Mawr Avenue
IL
Chicago
60631
773/380-
9933
&421
Douglas
G.
Soutter
312/814-
Office of the Attorney
General
Erivlrcinmental Bureau
Chicago
0660
Interested Party
69 W.
WashIngton,
18th Floor IL
60602
312/814-
2347
Matthew J
Dunn, Division Chief
Navyfcilities
and Eniineerinacommand
Great
Lakes
847/688-
201
Building
Decatur
1A
Avenue
IL
60088-
2600
Interested
Party
2801
847/688
2319
Mark Schultz,
Regional Environmental
Coordinator
Illinois
Pollution
Control
Board
100 W. Randolph
St.
Chicago
312/814-
Interested
Party
Suite
11-500
IL
60601
3620
3
12/814-
http:/Jwww.ipcb
.state. i
1.us/coollex
emalJcasenotifyNewasp?caseid=1
3524¬ifytypeS..
11/12/2008
-
‘-“- -“.‘
•
-L
J1
.)
3669
Dorothy
M.
Gunn,
Clerk of
the
Board
Richard
McGill,
Hearing
Officer
Commonwealth
Edison
1.0
South Dearborn
Street
Chicago
Interested
Party
35FNW
IL
60603
Diane H. Richardson
Downers
Clayton
Group Services
Interested
Party
3140 Finley
Road
Grove
IL
60515
Monte Nlenkerk
Waver
Boos
&
Gordon
2021. Tlmberbrook
Lane
Springfield
Interested
Party
IL
62702
Elizabeth
Steinhour
3300
GInger
Creek Drive
Springfield
Interested Party
IL
62711
Kenneth
W.
Liss
raef
Anhait
Schloemer
&
AssociatesJti
8501
West Higgins
Road
Chicago
IL
60631-
Suite 280
Interested
Party
2801
Dr. Douglas
C.
Hambley,
P.E., P.G.
Missrnan
Stanley &Associates
Rockford
333 East
State
Street
IL
61110-
Interested
Party
0827
John
W,
Hochwarter
Jeffrey Larson
Trivedi
Associates, Inc.
2055
Steeptebrook Court
Naperville
interested
Party
IL
60565
Chetan Trivedi
217/782-
Illinois
Department
of Natural
Resources
Springfield
One Natural
Resources
Way
IL
62702-
1809
Interested Party
1271
217)524-
9640
Stan
‘Yonkauski
William Richardson,
Chief Legal Counsel
Suburban
Laboratories.
inc.
4140 Lltt
Drive
Hillside
708-544-
Interested
Party
IL
60162
3260
Jarrett Thomas,
V.P.
2300 S Di
rksen Parkway
Springfield
Interested Party
Room
302
IL
62764
Steven
Gobel
man
jdsjJP
77
W.
Wacker
ChIcago
312/849
Interested
Party
Suite
4100
IL 60601
8100
David
Rieser
Reott
Law
Offices LLC
35
East
Wacker Drive
Chicago
312/332-
7544
Interested
Party
Suite 650
IL
60601
Raymond
T, Reoti
Jorge
T. Mihalopoulos
Environmental
Management
&
2012 W.
College Avenue
Normal
309/454-
Thnolopies,
Inc.
Suite
208
IL
61761
1717
Interested
Party
Craig
Cocker,
President
http://www.ipcb.state.il
.us/coo1JexternálJcasenotif’New.asp?caseid=
1 3524¬ifytyp
e=S..
11/12/2008
rriiiiing ervce
L.dSL...
rage
3
ot
3
217/522 -
IL
EnviroflmentJ Reaulatorv
GrouD
215
East Adams Street
Springfield
5512
Interested Party
IL 62701
217/522-
5518
Alec M.
Davis
312/742-
Chicano
Deoartment
of Law
30 N.
LaSalle Street
Chicago
3990
Interested Party
SuIte
900
IL 60602
312/744-
6798
Charles
A.
King, Assistant
Corporation
Counsel
SRAC
Decatur
2510
Brooks Drive
Interested Party
XL
62521
Harry
Walton
rns
&
McDonnell Engineerinci Company,
210
South Clark Street,
Suite
Chicago
Interested Party
The
2235
Clark
Adams Building
IL
60603
6306751625
Lawrence
L. Fieber, Principal
Total number
of participants:
34
http
://wwwipcb.state.iLusJcoo1/externaJ/casenotifvNewasp?caseid=l
3524¬ifytvpeS...
li/i 2/200