[Federal Register: February 28, 2006 (Volume 71, Number 39)]
[Rules and Regulations]               
[Page 10099-10385]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr28fe06-25]                         
 

[[Page 10099]]

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Part II





Department of Labor





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Occupational Safety and Health Administration



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29 CFR Parts 1910, 1915, et al.



Occupational Exposure to Hexavalent Chromium; Final Rule


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DEPARTMENT OF LABOR

Occupational Safety and Health Administration

29 CFR Parts 1910, 1915, 1917, 1918, and 1926

[Docket No. H054A]
RIN 1218-AB45

 
Occupational Exposure to Hexavalent Chromium

AGENCY: Occupational Safety and Health Administration (OSHA), 
Department of Labor.

ACTION: Final rule.

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SUMMARY: The Occupational Safety and Health Administration (OSHA) is 
amending the existing standard which limits occupational exposure to 
hexavalent chromium (Cr(VI)). OSHA has determined based upon the best 
evidence currently available that at the current permissible exposure 
limit (PEL) for Cr(VI), workers face a significant risk to material 
impairment of their health. The evidence in the record for this 
rulemaking indicates that workers exposed to Cr(VI) are at an increased 
risk of developing lung cancer. The record also indicates that 
occupational exposure to Cr(VI) may result in asthma, and damage to the 
nasal epithelia and skin.
    The final rule establishes an 8-hour time-weighted average (TWA) 
exposure limit of 5 micrograms of Cr(VI) per cubic meter of air (5 
[mu]g/m\3\). This is a considerable reduction from the previous PEL of 
1 milligram per 10 cubic meters of air (1 mg/10 m\3\, or 100 [mu]g/
m\3\) reported as CrO3, which is equivalent to a limit of 52 
[mu]g/m\3\ as Cr(VI). The final rule also contains ancillary provisions 
for worker protection such as requirements for exposure determination, 
preferred exposure control methods, including a compliance alternative 
for a small sector for which the new PEL is infeasible, respiratory 
protection, protective clothing and equipment, hygiene areas and 
practices, medical surveillance, recordkeeping, and start-up dates that 
include four years for the implementation of engineering controls to 
meet the PEL.
    The final standard separately regulates general industry, 
construction, and shipyards in order to tailor requirements to the 
unique circumstances found in each of these sectors.
    The PEL established by this rule reduces the significant risk posed 
to workers by occupational exposure to Cr(VI) to the maximum extent 
that is technologically and economically feasible.

DATES: This final rule becomes effective on May 30, 2006. Start-up 
dates for specific provisions are set in Sec.  1910.1026(n) for general 
industry; Sec.  1915.1026(l) for shipyards; and Sec.  1926.1126(l) for 
construction. However, affected parties do not have to comply with the 
information collection requirements in the final rule until the 
Department of Labor publishes in the Federal Register the control 
numbers assigned by the Office of Management and Budget (OMB). 
Publication of the control numbers notifies the public that OMB has 
approved these information collection requirements under the Paperwork 
Reduction Act of 1995.

ADDRESSES: In compliance with 28 U.S.C. 2112(a), the Agency designates 
the Associate Solicitor for Occupational Safety and Health, Office of 
the Solicitor, Room S-4004, U.S. Department of Labor, 200 Constitution 
Avenue, NW., Washington, DC 20210, as the recipient of petitions for 
review of these standards.

FOR FURTHER INFORMATION CONTACT: Mr. Kevin Ropp, Director, OSHA Office 
of Communications, Room N-3647, U.S. Department of Labor, 200 
Constitution Avenue, NW., Washington, DC 20210; telephone (202) 693-
1999.

SUPPLEMENTARY INFORMATION: The following table of contents lays out the 
structure of the preamble to the final standards. This preamble 
contains a detailed description of OSHA's legal obligations, the 
analyses and rationale supporting the Agency's determination, including 
a summary of and response to comments and data submitted during the 
rulemaking.

I. General
II. Pertinent Legal Authority
III. Events Leading to the Final Standard
IV. Chemical Properties and Industrial Uses
V. Health Effects
    A. Absorption, Distribution, Metabolic Reduction and Elimination
    1. Deposition and Clearance of Inhaled Cr(VI) From the 
Respiratory Tract
    2. Absorption of Inhaled Cr(VI) Into the Bloodstream
    3. Dermal Absorption of Cr(VI)
    4. Absorption of Cr(VI) by the Oral Route
    5. Distribution of Cr(VI) in the Body
    6. Metabolic Reduction of Cr(VI)
    7. Elimination of Cr(VI) From the Body
    8. Physiologically-Based Pharmacokinetic Modeling
    9. Summary
    B. Carcinogenic Effects
    1. Evidence From Chromate Production Workers
    2. Evidence From Chromate Pigment Production Workers
    3. Evidence From Workers in Chromium Plating
    4. Evidence From Stainless Steel Welders
    5. Evidence From Ferrochromium Workers
    6. Evidence From Workers in Other Industry Sectors
    7. Evidence From Experimental Animal Studies
    8. Mechanistic Considerations
    C. Non-Cancer Respiratory Effects
    1. Nasal Irritation, Nasal Tissue Ulcerations and Nasal Septum 
Perforations
    2. Occupational Asthma
    3. Bronchitis
    4. Summary
    D. Dermal Effects
    E. Other Health Effects
VI. Quantitative Risk Assessment
    A. Introduction
    B. Study Selection
    1. Gibb Cohort
    2. Luippold Cohort
    3. Mancuso Cohort
    4. Hayes Cohort
    5. Gerin Cohort
    6. Alexander Cohort
    7. Studies Selected for the Quantitative Risk Assessment
    C. Quantitative Risk Assessments Based on the Gibb Cohort
    1. Environ Risk Assessments
    2. National Institute for Occupational Safety and Health (NIOSH) 
Risk Assessment
    3. Exponent Risk Assessment
    4. Summary of Risk Assessments Based on the Gibb Cohort
    D. Quantitative Risk Assessments Based on the Luippold Cohort
    E. Quantitative Risk Assessments Based on the Mancuso, Hayes, 
Gerin, and Alexander Cohorts
    1. Mancuso Cohort
    2. Hayes Cohort
    3. Gerin Cohort
    4. Alexander Cohort
    F. Summary of Risk Estimates Based on Gibb, Luippold, and 
Additional Cohorts
    G. Issues and Uncertainties
    1. Uncertainty With Regard to Worker Exposure to Cr(VI)
    2. Model Uncertainty, Exposure Threshold, and Dose Rate Effects
    3. Influence of Smoking, Race, and the Healthy Worker Survivor 
Effect
    4. Suitability of Risk Estimates for Cr(VI) Exposures in Other 
Industries
    H. Conclusions
VII. Significance of Risk
    A. Material Impairment of Health
    1. Lung Cancer
    2. Non-Cancer Impairments
    B. Risk Assessment
    1. Lung Cancer Risk Based on the Gibb Cohort
    2. Lung Cancer Risk Based on the Luippold Cohort
    3. Risk of Non-Cancer Impairments
    C. Significance of Risk and Risk Reduction
VIII. Summary of the Final Economic Analysis and Regulatory 
Flexibility Analysis
IX. OMB Review Under the Paperwork Reduction Act of 1995
X. Federalism
XI. State Plans

[[Page 10101]]

XII. Unfunded Mandates
XIII. Protecting Children from Environmental Health and Safety Risks
XIV. Environmental Impacts
XV. Summary and Explanation of the Standards
    (a) Scope
    (b) Definitions
    (c) Permissible Exposure Limit (PEL)
    (d) Exposure Determination
    (e) Regulated Areas
    (f) Methods of Compliance
    (g) Respiratory Protection
    (h) Protective Work Clothing and Equipment
    (i) Hygiene Areas and Practices
    (j) Housekeeping
    (k) Medical Surveillance
    (l) Communication of Chromium (VI) Hazards to Employees
    (m) Recordkeeping
    (n) Dates
XVI. Authority and Signature
XVII. Final Standards

I. General

    This final rule establishes a permissible exposure limit (PEL) of 5 
micrograms of Cr(VI) per cubic meter of air (5 [mu]g/m\3\) as an 8-hour 
time-weighted average for all Cr(VI) compounds. After consideration of 
all comments and evidence submitted during this rulemaking, OSHA has 
made a final determination that a PEL of 5 [mu]g/m\3\ is necessary to 
reduce the significant health risks posed by occupational exposures to 
Cr(VI); it is the lowest level that is technologically and economically 
feasible for industries impacted by this rule. A full explanation of 
OSHA's rationale for establishing this PEL is presented in the 
following preamble sections: V (Health Effects), VI (Quantitative Risk 
Assessment), VII (Significance of Risk), VIII (Summary of the Final 
Economic Analysis and Regulatory Flexibility Analysis), and XV (Summary 
and Explanation of the Standard, paragraph (c), Permissible Exposure 
Limit).
    OSHA is establishing three separate standards covering occupational 
exposures to Cr(VI) for: general industry (29 CFR 1910.1026); shipyards 
(29 CFR 1915.1026), and construction (29 CFR 1926.1126). In addition to 
the PEL, these three standards include ancillary provisions for 
exposure determination, methods of compliance, respiratory protection, 
protective work clothing and equipment, hygiene areas and practices, 
medical surveillance, communication of Cr(VI) hazards to employees, 
recordkeeping, and compliance dates. The general industry standard has 
additional provisions for regulated areas and housekeeping. The Summary 
and Explanation section of this preamble (Section XV, paragraphs (d) 
through (n)) includes a full discussion of the basis for including 
these provisions in the final standards.
    Several major changes were made to the October 4, 2004 proposed 
rule as a result of OSHA's analysis of comments and data received 
during the comment periods and public hearings. The major changes are 
summarized below and are fully discussed in the Summary and Explanation 
section of this preamble (Section XV)
    Scope. As proposed, the standards apply to occupational exposures 
to Cr(VI) in all forms and compounds with limited exceptions. OSHA has 
made a final determination to exclude from coverage of these final 
standards exposures that occur in the application of pesticides 
containing Cr(VI) (e.g., the treatment of wood with preservatives). 
These exposures are already covered by the Environmental Protection 
Agency. OSHA is also excluding exposures to portland cement and 
exposures in work settings where the employer has objective data 
demonstrating that a material containing chromium or a specific 
process, operation, or activity involving chromium cannot release 
dusts, fumes, or mists of Cr(VI) in concentrations at or above 0.5 
[mu]g/m\3\ under any expected conditions of use. OSHA believes that the 
weight of evidence in this rulemaking demonstrates that the primary 
risk in these two exposure scenarios can be effectively addressed 
through existing OSHA standards for personal protective equipment, 
hygiene, hazard communication and the PELs for portland cement or 
particulates not otherwise regulated (PNOR).
    Permissible Exposure Limit. OSHA proposed a PEL of 1 [mu]g/m\3\ but 
has now determined that a PEL 5 [mu]g/m\3\ is the lowest level that is 
technologically and economically feasible.
    Exposure Determination. OSHA did not include a provision for 
exposure determination in the proposed shipyard and construction 
standards, reasoning that the obligation to meet the proposed PEL would 
implicitly necessitate performance-based monitoring by the employer to 
ensure compliance with the PEL. However, OSHA was convinced by 
arguments presented during the rulemaking that an explicit requirement 
for exposure determination is necessary to ensure that employee 
exposures are adequately characterized. Therefore OSHA has included a 
provision for exposure determination for general industry, shipyards 
and construction in the final rule. In order to provide additional 
flexibility in characterizing employee exposures, OSHA is allowing 
employers to choose between a scheduled monitoring option and a 
performance-based option for making exposure determinations.
    Methods of Compliance. Under the proposed rule employers were to 
use engineering and work practice controls to achieve the proposed PEL 
unless the employer could demonstrate such controls are not feasible. 
In the final rule, OSHA has retained this exception but has added a 
provision that only requires employers to use engineering and work 
practice controls to reduce or maintain employee exposures to 25 [mu]g/
m\3\ when painting aircraft or large aircraft parts in the aerospace 
industry to the extent such controls are feasible. The employer must 
then supplement those engineering controls with respiratory protection 
to achieve the PEL. As discussed more fully in the Summary of the Final 
Economic Analysis and Regulatory Flexibility Analysis (Section VIII) 
and the Summary and Explanation (Section XV) OSHA has determined that 
this is the lowest level achievable through the use of engineering and 
work practice controls alone for these limited operations.
    Housekeeping. In the proposed rule, cleaning methods such as 
shoveling, sweeping, and brushing were prohibited unless they were the 
only effective means available to clean surfaces contaminated with 
Cr(VI). The final standard has modified this prohibition to make clear 
only dry shoveling, sweeping and brushing are prohibited so that 
effective wet shoveling, sweeping, and brushing would be allowed. OSHA 
is also adding a provision that allows the use of compressed air to 
remove Cr(VI) when no alternative method is feasible.
    Medical Surveillance. As proposed and continued in these final 
standards, medical surveillance is required to be provided to employees 
experiencing signs or symptoms of the adverse health effects associated 
with Cr(VI) exposure or exposed in an emergency. In addition, for 
general industry, employees exposed above the PEL for 30 or more days a 
year were to be provided medical surveillance. In the final standard, 
OSHA has changed the trigger for medical surveillance to exposure above 
the action level (instead of the PEL) for 30 days a year to take into 
account the existing risks at the new PEL. This provision has also been 
extended to the standards for shipyards and construction since those 
employers now will be required to perform an exposure determination and 
thus will be able to determine which employees are exposed above the 
action level 30 or more days a year.

[[Page 10102]]

    Communication of Hazards. In the proposed standard, OSHA specified 
the sign for the demarcation of regulated areas in general industry and 
the label for contaminated work clothing or equipment and Cr(VI) 
contaminated waste and debris. The proposed standard also listed the 
various elements to be covered for employee training. In order to 
simplify requirements under this section of the final standard and 
reduce confusion between this standard and the Hazard Communication 
Standard, OSHA has removed the requirement for special signs and labels 
and the specification of employee training elements. Instead, the final 
standard requires that signs, labels and training be in accordance with 
the Hazard Communication Standard (29 CFR 1910.1200). The only 
additional training elements required in the final rule are those 
related specifically to the contents of the final Cr(VI) standards. 
While the final standards have removed language in the communication of 
hazards provisions to make them more consistent with OSHA's existing 
Hazard Communication Standard, the employers obligation to mark 
regulated areas (where regulated areas are required), to label Cr(VI) 
contaminated clothing and wastes, and to train on the hazards of Cr(VI) 
have not changed.
    Recordkeeping. In the proposed standards for shipyards and 
construction there were no recordkeeping requirements for exposure 
records since there was not a requirement for exposure determination. 
The final standard now requires exposure determination for shipyards 
and construction and therefore, OSHA has also added provisions for 
exposure records to be maintained in these final standards. In keeping 
with its intent to be consistent with the Hazard Communication 
Standard, OSHA has removed the requirement for training records in the 
final standards.
    Dates. In the proposed standard, the effective date of the standard 
was 60 days after the publication date; the start-up date for all 
provisions except engineering controls was 90 days after the effective 
date; and the start-up date for engineering controls was two years 
after the effective date. OSHA believes that it is appropriate to allow 
additional time for employers, particularly small employers, to meet 
the requirements of the final rule. The effective and start-up dates 
have been extended as follows: the effective date for the final rule is 
changed to 90 days after the publication date; the start-up date for 
all provisions except engineering controls is changed to 180 days after 
the effective date for employers with 20 or more employees; the start-
up date for all provisions except engineering controls is changed to 
one year after the effective date for employers with 19 or fewer 
employees; and the start-up date for engineering controls is changed to 
four years after the effective date for all employers.

II. Pertinent Legal Authority

    The purpose of the Occupational Safety and Health Act, 29 U.S.C. 
651 et seq. (``the Act'') is to,

* * * assure so far as possible every working man and woman in the 
nation safe and healthful working conditions and to preserve our 
human resources. 29 U.S.C. 651(b).

    To achieve this goal Congress authorized the Secretary of Labor 
(the Secretary) to promulgate and enforce occupational safety and 
health standards. 29 U.S.C. 654(b) (requiring employers to comply with 
OSHA standards), 655(a) (authorizing summary adoption of existing 
consensus and federal standards within two years of the Act's 
enactment), and 655(b) (authorizing promulgation, modification or 
revocation of standards pursuant to notice and comment).
    The Act provides that in promulgating health standards dealing with 
toxic materials or harmful physical agents, such as this standard 
regulating occupational exposure to Cr(VI), the Secretary,

* * * shall set the standard which most adequately assures, to the 
extent feasible, on the basis of the best available evidence that no 
employee will suffer material impairment of health or functional 
capacity even if such employee has regular exposure to the hazard 
dealt with by such standard for the period of his working life. 29 
U.S.C. Sec.  655(b)(5).

    The Supreme Court has held that before the Secretary can promulgate 
any permanent health or safety standard, she must make a threshold 
finding that significant risk is present and that such risk can be 
eliminated or lessened by a change in practices. Industrial Union 
Dept., AFL-CIO v. American Petroleum Institute, 448 U.S. 607, 641-42 
(1980) (plurality opinion) (``The Benzene case''). The Court further 
observed that what constitutes ``significant risk'' is ``not a 
mathematical straitjacket'' and must be ``based largely on policy 
considerations.'' The Benzene case, 448 U.S. at 655. The Court gave the 
example that if,

* * * the odds are one in a billion that a person will die from 
cancer * * * the risk clearly could not be considered significant. 
On the other hand, if the odds are one in one thousand that regular 
inhalation of gasoline vapors that are 2% benzene will be fatal, a 
reasonable person might well consider the risk significant. * * * 
Id.

    OSHA standards must be both technologically and economically 
feasible. United Steelworkers v. Marshall, 647 F.2d 1189, 1264 (D.C. 
Cir. 1980) (``The Lead I case''). The Supreme Court has defined 
feasibility as ``capable of being done.'' American Textile Mfrs. Inst. 
v. Donovan, 425 U.S. 490, 509 (1981) (``The Cotton dust case''). The 
courts have further clarified that a standard is technologically 
feasible if OSHA proves a reasonable possibility,

* * * within the limits of the best available evidence * * * that 
the typical firm will be able to develop and install engineering and 
work practice controls that can meet the PEL in most of its 
operations. See The Lead I case, 647 F.2d at 1272.

    With respect to economic feasibility, the courts have held that a 
standard is feasible if it does not threaten massive dislocation to or 
imperil the existence of the industry. See The Lead case, 647 F.2d at 
1265. A court must examine the cost of compliance with an OSHA standard 
``in relation to the financial health and profitability of the industry 
and the likely effect of such costs on unit consumer prices.'' Id.

    [The] practical question is whether the standard threatens the 
competitive stability of an industry, * * * or whether any intra-
industry or inter-industry discrimination in the standard might 
wreck such stability or lead to undue concentration. Id. (citing 
Industrial Union Dept., AFL-CIO v. Hodgson, 499 F.2d 467 (D.C. Cir. 
1974)).

    The courts have further observed that granting companies reasonable 
time to comply with new PEL's may enhance economic feasibility. Id. 
While a standard must be economically feasible, the Supreme Court has 
held that a cost-benefit analysis of health standards is not required 
by the Act because a feasibility analysis is. The Cotton dust case, 453 
U.S. at 509. Finally, unlike safety standards, health standards must 
eliminate risk or reduce it to the maximum extent that is 
technologically and economically feasible. See International Union, 
United Automobile, Aerospace & Agricultural Implement Workers of 
America, UAW v. OSHA, 938 F.2d 1310, 1313 (D.C. Cir. 1991); Control of 
Hazardous Energy Sources (Lockout/Tagout), Final rule; supplemental 
statement of reasons, (58 FR 16612, March 30, 1993).

III. Events Leading to the Final Standard

    OSHA's previous standards for workplace exposure to Cr(VI) were 
adopted in 1971, pursuant to section 6(a) of the Act, from a 1943 
American National Standards Institute (ANSI) recommendation originally 
established to control irritation and damage to nasal

[[Page 10103]]

tissues (36 FR at 10466, 5/29/71; Ex. 20-3). OSHA's general industry 
standard set a permissible exposure limit (PEL) of 1 mg chromium 
trioxide per 10 m\3\ air in the workplace (1 mg/10 m\3\ 
CrO3) as a ceiling concentration, which corresponds to a 
concentration of 52 [mu]g/m\3\ Cr(VI). A separate rule promulgated for 
the construction industry set an eight-hour time-weighted-average PEL 
of 1 mg/10 m3 CrO3, also equivalent to 52 [mu]g/
m\3\ Cr(VI), adopted from the American Conference of Governmental 
Industrial Hygienists (ACGIH) 1970 Threshold Limit Value (TLV) (36 FR 
at 7340, 4/17/71).
    Following the ANSI standard of 1943, other occupational and public 
health organizations evaluated Cr(VI) as a workplace and environmental 
hazard and formulated recommendations to control exposure. The ACGIH 
first recommended control of workplace exposures to chromium in 1946, 
recommending a time-weighted average Maximum Allowable Concentration 
(later called a Threshold Limit Value) of 100 [mu]g/m\3\ for chromic 
acid and chromates as Cr2O3 (Ex. 5-37), and later 
classified certain Cr(VI) compounds as class A1 (confirmed human) 
carcinogens in 1974. In 1975, the NIOSH Criteria for a Recommended 
Standard recommended that occupational exposure to Cr(VI) compounds 
should be limited to a 10-hour TWA of 1 [mu]g/m\3\, except for some 
forms of Cr(VI) then believed to be noncarcinogenic (Ex. 3-92). The 
National Toxicology Program's First Annual Report on Carcinogens 
identified calcium chromate, chromium chromate, strontium chromate, and 
zinc chromate as carcinogens in 1980 (Ex. 35-157).
    During the 1980s, regulatory and standards organizations came to 
recognize Cr(VI) compounds in general as carcinogens. The Environmental 
Protection Agency (EPA) Health Assessment Document of 1984 stated that,

* * * using the IARC [International Agency for Research on Cancer] 
classification scheme, the level of evidence available for the 
combined animal and human data would place hexavalent chromium (Cr 
VI) compounds into Group 1, meaning that there is decisive evidence 
for the carcinogenicity of those compounds in humans (Ex. 19-1, p. 
7-107).

    In 1988 IARC evaluated the available evidence regarding Cr(VI) 
carcinogenicity, concluding in 1990 that

* * * [t]here is sufficient evidence in humans for the 
carcinogenicity of chromium[VI] compounds as encountered in the 
chromate production, chromate pigment production and chromium 
plating industries, [and] sufficient evidence in experimental 
animals for the carcinogenicity of calcium chromate, zinc chromates, 
strontium chromate and lead chromates (Ex. 18-3, p. 213).

    In September 1988, NIOSH advised OSHA to consider all Cr(VI) 
compounds as potential occupational carcinogens (Ex. 31-22-22). ACGIH 
now classifies water-insoluble and water-soluble Cr(IV) compounds as 
class A1 carcinogens (Ex. 35-207). Current ACGIH standards include 
specific 8-hour time-weighted average TLVs for calcium chromate (1 
[mu]g/m3), lead chromate (12 [mu]g/m3), strontium 
chromate (0.5 [mu]g/m3), and zinc chromates (10 [mu]g/
m3), and generic TLVs for water soluble (50 [mu]g/
m3) and insoluble (10 [mu]g/m3) forms of 
hexavalent chromium not otherwise classified, all measured as chromium 
(Ex. 35-207).
    In July 1993, OSHA was petitioned for an emergency temporary 
standard to reduce occupational exposures to Cr(VI) compounds (Ex. 1). 
The Oil, Chemical, and Atomic Workers International Union (OCAW) and 
Public Citizen's Health Research Group (Public Citizen), citing 
evidence that occupational exposure to Cr(VI) increases workers' risk 
of lung cancer, petitioned OSHA to promulgate an emergency temporary 
standard to lower the PEL for Cr(VI) compounds to 0.5 [mu]g/
m3 as an eight-hour time-weighted average (TWA). Upon review 
of the petition, OSHA agreed that there was evidence of increased 
cancer risk from exposure to Cr(VI) at the existing PEL, but found that 
the available data did not show the ``grave danger'' required to 
support an emergency temporary standard (Ex. 1-C). The Agency therefore 
denied the request for an emergency temporary standard, but initiated 
Section 6(b)(5) rulemaking and began performing preliminary analyses 
relevant to the rule.
    In 1997, Public Citizen petitioned the United States Court of 
Appeals for the Third Circuit to compel OSHA to complete rulemaking 
lowering the standard for occupational exposure to Cr(VI). The Court 
denied Public Citizen's request, concluding that there was no 
unreasonable delay and dismissed the suit. Oil, Chemical and Atomic 
Workers Union and Public Citizen Health Research Group v. OSHA, 145 
F.3d 120 (3rd Cir. 1998). Afterwards, the Agency continued its data 
collection and analytic efforts on Cr(VI) (Ex. 35-208, p. 3). In 2002, 
Public Citizen again petitioned the Court to compel OSHA to commence 
rulemaking to lower the Cr(VI) standard (Ex. 31-24-1). Meanwhile on 
August 22, 2002, OSHA published a Request for Information on Cr(VI) to 
solicit additional information on key issues related to controlling 
exposures to Cr(VI) (FR 67 at 54389), and on December 4, 2002 announced 
its intent to proceed with developing a proposed standard (Ex. 35-306). 
On December 24, 2002, the Court granted Public Citizen's petition, and 
ordered the Agency to proceed expeditiously with a Cr(VI) standard. See 
Public Citizen Health Research Group v. Chao, 314 F.3d 143 (3rd Cir. 
2002)). In a subsequent order, the Court established a compressed 
schedule for completion of the rulemaking, with deadlines of October 4, 
2004 for publication of a proposed standard and January 18, 2006 for 
publication of a final standard (Ex. 35-304).
    In 2003, as required by the Small Business Regulatory Enforcement 
Act (SBREFA), OSHA initiated SBREFA proceedings, seeking the advice of 
small business representatives on the proposed rule. The SBREFA panel, 
including representatives from OSHA, the Small Business Administration 
(SBA), and the Office of Management and Budget (OMB), was convened on 
December 23, 2003. The panel conferred with representatives from small 
entities in chemical, alloy, and pigment manufacturing, electroplating, 
welding, aerospace, concrete, shipbuilding, masonry, and construction 
on March 16-17, 2004, and delivered its final report to OSHA on April 
20, 2004. The Panel's report, including comments from the small entity 
representatives (SERS) and recommendations to OSHA for the proposed 
rule, is available in the Cr(VI) rulemaking docket (Ex. 34). The SBREFA 
Panel made recommendations on a variety of subjects. The most important 
recommendations with respect to alternatives that OSHA should consider 
included: A higher PEL than the PEL of 1; excluding cement from the 
scope of the standard; the use of SECALs for some industries; different 
PELS for different Hexavalent chromium compounds; a multi-year phase-in 
to the standards; and further consideration to approaches suited to the 
special conditions of the maritime and construction industries. OSHA 
has adapted many of these recommendations: The PEL is now 5; cement has 
been excluded from the scope of the standard; a compliance alternative, 
similar to a SECAL, has been used in aerospace industry; the standard 
allows four years to phase in engineering controls; and a new 
performance based monitoring approach for all industries, among other 
changes, all of which should make it easier for all

[[Page 10104]]

industries with changing work place conditions to meet the standard in 
a cost effective way. A full discussion of all of the recommendations, 
and OSHA's responses to them, is provided in Section VIII of this 
Preamble.
    In addition to undertaking SBREFA proceedings, in early 2004, OSHA 
provided the Advisory Committee on Construction Safety and Health 
(ACCSH) and the Maritime Advisory Committee on Occupational Safety and 
Health (MACOSH) with copies of the draft proposed rule for review. OSHA 
representatives met with ACCSH in February 2004 and May 2004 to discuss 
the rulemaking and receive their comments and recommendations. On 
February 13, 2004, ACCSH recommended that portland cement should be 
included within the scope of the proposed standard (Ex. 35-307, pp. 
288-293) and that identical PELs should be set for construction, 
maritime, and general industry (Ex. 35-307, pp. 293-297). On May 18, 
2004, ACCSH recommended that the construction industry should be 
included in the current rulemaking, and affirmed its earlier 
recommendation regarding portland cement. OSHA representatives met with 
MACOSH in March 2004. On March 3, 2004, MACOSH collected and forwarded 
additional exposure monitoring data to OSHA to help the Agency better 
evaluate exposures to Cr(VI) in shipyards (Ex. 35-309, p. 208). MACOSH 
also recommended a separate Cr(VI) standard for the maritime industry, 
arguing that maritime involves different exposures and requires 
different means of exposure control than general industry and 
construction (Ex. 35-309, p. 227).
    In accordance with the Court's rulemaking schedule, OSHA published 
the proposed standard for hexavalent chromium on October 4, 2004 (69 FR 
at 59306). The proposal included a notice of public hearing in 
Washington, DC (69 FR at 59306, 59445-59446). The notice also invited 
interested persons to submit comments on the proposal until January 3, 
2005. In the proposal, OSHA solicited public input on 65 issues 
regarding the human health risks of Cr(VI) exposure, the impact of the 
proposed rule on Cr(VI) users, and other issues of particular interest 
to the Agency (69 FR at 59306-59312).
    OSHA convened the public hearing on February 1, 2005, with 
Administrative Law Judges John M. Vittone and Thomas M. Burke 
presiding. At the conclusion of the hearing on February 15, 2005, Judge 
Burke set a deadline of March 21, 2005, for the submission of post 
hearing comments, additional information and data relevant to the 
rulemaking, and a deadline of April 20, 2005, for the submission of 
additional written comments, arguments, summations, and briefs. A wide 
range of employees, employers, union representatives, trade 
associations, government agencies and other interested parties 
participated in the public hearing or contributed written comments. 
Issues raised in their comments and testimony are addressed in the 
relevant sections of this preamble (e.g., comments on the risk 
assessment are discussed in section VI; comments on the benefits 
analysis in section VIII). On December 22, 2005, OSHA filed a motion 
with the U.S. Court of Appeals for the Third Circuit requesting an 
extension of the court-mandated deadline for the publication of the 
final rule by six weeks, to February 28, 2006 (Ex. 48-13). The Court 
granted the request on January 17, 2006 (Ex. 48-15).
    As mandated by the Act, the final standard on occupational exposure 
to hexavalent chromium is based on careful consideration of the entire 
record of this proceeding, including materials discussed or relied upon 
in the proposal, the record of the hearing, and all written comments 
and exhibits received.
    OSHA has developed separate final standards for general industry, 
shipyards, and the construction industry. The Agency has concluded that 
excess exposure to Cr(VI) in any form poses a significant risk of 
material impairment to the health of workers, by causing or 
contributing to adverse health effects including lung cancer, non-
cancer respiratory effects, and dermal effects. OSHA determined that 
the TWA PEL should not be set above 5 [mu]g/m3 based on the 
evidence in the record and its own quantitative risk assessment. The 
TWA PEL of 5 [mu]g/m3 reduces the significant risk posed to 
workers by occupational exposure to Cr(VI) to the maximum extent that 
is technologically and economically feasible. (See discussion of the 
PEL in Section XV below.)

IV. Chemical Properties and Industrial Uses

    Chromium is a metal that exists in several oxidation or valence 
states, ranging from chromium (-II) to chromium (+VI). The elemental 
valence state, chromium (0), does not occur in nature. Chromium 
compounds are very stable in the trivalent state and occur naturally in 
this state in ores such as ferrochromite, or chromite ore 
(FeCr2O4). The hexavalent, Cr(VI) or chromate, is 
the second most stable state. It rarely occurs naturally; most Cr(VI) 
compounds are man made.
    Chromium compounds in higher valence states are able to undergo 
``reduction'' to lower valence states; chromium compounds in lower 
valence states are able to undergo ``oxidation'' to higher valence 
states. Thus, Cr(VI) compounds can be reduced to Cr(III) in the 
presence of oxidizable organic matter. Chromium can also be reduced in 
the presence of inorganic chemicals such as iron.
    Chromium does exist in less stable oxidation (valence) states such 
as Cr(II), Cr(IV), and Cr(V). Anhydrous Cr(II) salts are relatively 
stable, but the divalent state (II, or chromous) is generally 
relatively unstable and is readily oxidized to the trivalent (III or 
chromic) state. Compounds in valence states such as (IV) and (V) 
usually require special handling procedures as a result of their 
instability. Cr(IV) oxide (CrO2) is used in magnetic 
recording and storage devices, but very few other Cr(IV) compounds have 
industrial use. Evidence exists that both Cr(IV) and Cr(V) are formed 
as transient intermediates in the reduction of Cr(VI) to Cr(III) in the 
body.
    Chromium (III) is also an essential nutrient that plays a role in 
glucose, fat, and protein metabolism by causing the action of insulin 
to be more effective. Chromium picolinate, a trivalent form of chromium 
combined with picolinic acid, is used as a dietary supplement, because 
it is claimed to speed metabolism.
    Elemental chromium and the chromium compounds in their different 
valence states have various physical and chemical properties, including 
differing solubilities. Most chromium species are solid. Elemental 
chromium is a steel gray solid, with high melting and boiling points 
(1857 [deg]C and 2672 [deg]C, respectively), and is insoluble in water 
and common organic solvents. Chromium (III) chloride is a violet or 
purple solid, with high melting and sublimation points (1150 [deg]C and 
1300 [deg]C, respectively), and is slightly soluble in hot water and 
insoluble in common organic solvents. Ferrochromite is a brown-black 
solid; chromium (III) oxide is a green solid; and chromium (III) 
sulfate is a violet or red solid, insoluble in water and slightly 
soluble in ethanol. Chromium (III) picolinate is a ruby red crystal 
soluble in water (1 part per million at 25 [deg]C). Chromium (IV) oxide 
is a brown-black solid that decomposes at 300 [deg]C and is insoluble 
in water.
    Cr(VI) compounds have mostly lemon yellow to orange to dark red 
hues. They are typically crystalline, granular, or powdery although one 
compound (chromyl chloride) exists in liquid form. For example, chromyl 
chloride is a dark

[[Page 10105]]

red liquid that decomposes into chromate ion and hydrochloric acid in 
water. Chromic acids are dark red crystals that are very soluble in 
water. Other examples of soluble chromates are sodium chromate (yellow 
crystals) and sodium dichromate (reddish to bright orange crystals). 
Lead chromate oxide is typically a red crystalline powder. Zinc 
chromate is typically seen as lemon yellow crystals which decompose in 
hot water and are soluble in acids and liquid ammonia. Other chromates 
such as barium, calcium, lead, strontium, and zinc chromates vary in 
color from light yellow to greenish yellow to orange-yellow and exist 
in solid form as crystals or powder.
    The Color Pigments Manufacturers Association (CPMA) provided 
additional information on lead chromate and some other chromates used 
in their pigments (Ex. 38-205, pp. 12-13). CPMA describes two main lead 
chromate color groups: the chrome yellow pigments and the orange to red 
varieties known as molybdate orange pigments. The chrome yellow 
pigments are solid solution crystal compositions of lead chromate and 
lead sulfate. Molybdate orange pigments are solid solution crystal 
compositions of lead chromate, lead sulfate, and lead molybdate (Ex. 
38-205, p. 12). CPMA also describes a basic lead chromate called 
``chrome orange,'' and a lead chromate precipitated ``onto a core'' of 
silica (Ex. 38-205, p. 13).
    OSHA re-examined available information on solubility values in 
light of comments from the CPMA and Dominion Color Corporation (DCC) on 
qualitative solubility designations and CPMA's claim of low 
bioavailability of lead chromate due to its extremely low solubility 
(Exs. 38-201-1, p. 4; 38-205, p. 95). There was not always agreement or 
consistency with the qualitative assignments of solubilities. 
Quantitative values for the same compound also differ depending on the 
source of information.
    The Table IV-1 is the result of OSHA's re-examination of 
quantitative water solubility values and qualitative designations. 
Qualitative designations as well as quantitative values are listed as 
they were provided by the source. As can be seen by the Table IV-1, 
qualitative descriptions vary by the descriptive terminology chosen by 
the source.
BILLING CODE 4510-26-P

[[Page 10106]]

[GRAPHIC] [TIFF OMITTED] TR28FE06.000


[[Page 10107]]


[GRAPHIC] [TIFF OMITTED] TR28FE06.001

BILLING CODE 4510-26-C
    OSHA has made some generalizations to describe the water 
solubilities of chromates in subsequent sections of this Federal 
Register notice. OSHA has divided Cr(VI) compounds and mixtures into 
three categories based on solubility values. Compounds and mixtures 
with water solubilities less than 0.01 g/l are referred to as water 
insoluble. Compounds and mixtures between 0.01 g/l and 500 g/l are 
referred to as slightly

[[Page 10108]]

soluble. Compounds and mixtures with water solubility values of 500 g/l 
or greater are referred to as highly water soluble. It should be noted 
that these boundaries for insoluble, slightly soluble, and highly 
soluble are arbitrary designations for the sake of further description 
elsewhere in this document. Quantitative values take precedence over 
qualitative designations. For example, zinc chromates would be slightly 
soluble where their solubility values exceed 0.01 g/l.
    Some major users of chromium are the metallurgical, refractory, and 
chemical industries. Chromium is used by the metallurgical industry to 
produce stainless steel, alloy steel, and nonferrous alloys. Chromium 
is alloyed with other metals and plated on metal and plastic substrates 
to improve corrosion resistance and provide protective coatings for 
automotive and equipment accessories. Welders use stainless steel 
welding rods when joining metal parts.
    Cr(VI) compounds are widely used in the chemical industry in 
pigments, metal plating, and chemical synthesis as ingredients and 
catalysts. Chromates are used as high quality pigments for textile 
dyes, paints, inks, glass, and plastics. Cr(VI) can be produced during 
welding operations even if the chromium was originally present in 
another valence state. While Cr(VI) is not intentionally added to 
portland cement, it is often present as an impurity.
    Occupational exposures to Cr(VI) can occur from inhalation of mists 
(e.g., chrome plating, painting), dusts (e.g., inorganic pigments), or 
fumes (e.g., stainless steel welding), and from dermal contact (e.g., 
cement workers).
    There are about thirty major industries and processes where Cr(VI) 
is used. These include producers of chromates and related chemicals 
from chromite ore, electroplating, welding, painting, chromate pigment 
production and use, steel mills, and iron and steel foundries. A 
detailed discussion of the uses of Cr(VI) in industry is found in 
Section VIII of this preamble.

V. Health Effects

    This section summarizes key studies of adverse health effects 
resulting from exposure to hexavalent chromium (Cr(VI)) in humans and 
experimental animals, as well as information on the fate of Cr(VI) in 
the body and laboratory research that relates to its toxic mode of 
action. The primary health impairments from workplace exposure to 
Cr(VI) are lung cancer, asthma, and damage to the nasal epithelia and 
skin. While this chapter on health effects does not describe all of the 
many studies that have been conducted on Cr(VI) toxicity, it includes a 
selection of those that are relevant to the rulemaking and 
representative of the scientific literature on Cr(VI) health effects.

A. Absorption, Distribution, Metabolic Reduction and Elimination

    Although chromium can exist in a number of different valence 
states, Cr(VI) is the form considered to be the greatest health risk. 
Cr(VI) enters the body by inhalation, ingestion, or absorption through 
the skin. For occupational exposure, the airways and skin are the 
primary routes of uptake. The following discussion summarizes key 
aspects of Cr(VI) uptake, distribution, metabolism, and elimination.

1. Deposition and Clearance of Inhaled Cr(VI) From the Respiratory 
Tract

    Various anatomical, physical and physiological factors determine 
both the fractional and regional deposition of inhaled particulate 
matter. Due to the airflow patterns in the lung, more particles tend to 
deposit at certain preferred regions in the lung. It is therefore 
possible to have a buildup of chromium at certain sites in the 
bronchial tree that could create areas of very high chromium 
concentration. A high degree of correspondence between the efficiency 
of particle deposition and the frequency of bronchial tumors at sites 
in the upper bronchial tree was reported in research by Schlesinger and 
Lippman that compared the distribution of cancer sites in published 
reports of primary bronchogenic tumors with experimentally determined 
particle deposition patterns (Ex. 35-102).
    Large inhaled particles (>5 [mu]m) are efficiently removed from the 
air-stream in the extrathoracic region (Ex. 35-175). Particles greater 
than 2.5 [mu]m are generally deposited in the tracheobronchial regions, 
whereas particles less than 2.5 [mu]m are generally deposited in the 
pulmonary region. Some larger particles (>2.5 [mu]m) can reach the 
pulmonary region. The mucociliary escalator predominantly clears 
particles that deposit in the extrathoracic and the tracheobronchial 
region of the lung. Individuals exposed to high particulate levels of 
Cr(VI) may also have altered respiratory mucociliary clearance. 
Particulates that reach the alveoli can be absorbed into the 
bloodstream or cleared by phagocytosis.
2. Absorption of Inhaled Cr(VI) Into the Bloodstream
    The absorption of inhaled chromium compounds depends on a number of 
factors, including physical and chemical properties of the particles 
(oxidation state, size, solubility) and the activity of alveolar 
macrophages (Ex. 35-41). The hexavalent chromate anions 
(CrO4)2- enter cells via facilitated diffusion 
through non-specific anion channels (similar to phosphate and sulfate 
anions). As demonstrated in research by Suzuki et al., a portion of 
water soluble Cr(VI) is rapidly transported to the bloodstream in rats 
(Ex. 35-97). Rats were exposed to 7.3-15.9 mg Cr(VI)/m\3\ as potassium 
dichromate for 2-6 hours. Following exposure to Cr(VI), the ratio of 
blood chromium/lung chromium was 1.440.30 at 0.5 hours, 
0.810.10 at 18 hours, 0.850.20 at 48 hours, and 
0.960.22 at 168 hours after exposure.
    Once the Cr(VI) particles reach the alveoli, absorption into the 
bloodstream is greatly dependent on solubility. More soluble chromates 
are absorbed faster than water insoluble chromates, while insoluble 
chromates are poorly absorbed and therefore have longer resident time 
in the lungs. This effect has been demonstrated in research by Bragt 
and van Dura on the kinetics of three Cr(VI) compounds: highly soluble 
sodium chromate, slightly soluble zinc chromate and water insoluble 
lead chromate (Ex. 35-56). They instilled \51\chromium-labeled 
compounds (0.38 mg Cr(VI)/kg as sodium chromate, 0.36 mg Cr(VI)/kg as 
zinc chromate, or 0.21 mg Cr(VI)/kg as lead chromate) intratracheally 
in rats. Peak blood levels of \51\chromium were reached after 30 
minutes for sodium chromate (0.35 [mu]g chromium/ml), and after 24 
hours for zinc chromate (0.60 [mu]g chromium/ml) and lead chromate 
(0.007 [mu]g chromium/ml). At 30 minutes after administration, the 
lungs contained 36, 25, and 81% of the respective dose of the sodium, 
zinc, and lead chromate. On day six, >80% of the dose of all three 
compounds had been cleared from the lungs, during which time the 
disappearance from lungs followed linear first-order kinetics. The 
residual amount left in the lungs on day 50 or 51 was 3.0, 3.9, and 
13.9%, respectively. From these results authors concluded that zinc 
chromate, which is less soluble than sodium chromate, is more slowly 
absorbed from the lungs. Lead chromate was more poorly and slowly 
absorbed, as indicated by very low levels in blood and greater 
retention in the lungs. The authors also noted that the kinetics of 
sodium and zinc chromates were very similar. Zinc chromate, which is 
less soluble than sodium chromate, was slowly absorbed from the lung, 
but the maximal blood levels were higher than those resulting from an 
equivalent dose of sodium chromate. The authors

[[Page 10109]]

believe that this was probably the result of hemorrhages 
macroscopically visible in the lungs of zinc chromate-treated rats 24 
hours following intratracheal administration. Boeing Corporation 
commented that this study does not show that the highly water soluble 
sodium chromate is cleared more rapidly or retained in the lung for 
shorter periods than the less soluble zinc chromate (Ex. 38-106-2, p. 
18-19). This comment is addressed in the Carcinogenic Effects 
Conclusion Section V.B.9 dealing with the carcinogenicity of slightly 
soluble Cr(VI) compounds.
    Studies by Langard et al. and Adachi et al. provide further 
evidence of absorption of chromates from the lungs (Exs. 35-93; 189). 
In Langard et al., rats exposed to 2.1 mg Cr(VI)/m\3\ as zinc chromate 
for 6 hours/day achieved steady state concentrations in the blood after 
4 days of exposure (Ex. 35-93). Adachi et al. studied rats that were 
subject to a single inhalation exposure to chromic acid mist generated 
from electroplating at a concentration of 3.18 mg Cr(VI)/m\3\ for 30 
minutes which was then rapidly absorbed from the lungs (Ex. 189). The 
amount of chromium in the lungs of these rats declined from 13.0 mg 
immediately after exposure to 1.1 mg after 4 weeks, with an overall 
half-life of five days.
    Several other studies have reported absorption of chromium from the 
lungs after intratracheal instillation (Exs. 7-9; 9-81; Visek et al. 
1953 as cited in Ex. 35-41). These studies indicated that 53-85% of 
Cr(VI) compounds (particle size < 5 [mu]m) were cleared from the lungs 
by absorption into the bloodstream or by mucociliary clearance in the 
pharynx; the rest remained in the lungs. Absorption of Cr(VI) from the 
respiratory tract of workers has been shown in several studies that 
identified chromium in the urine, serum and red blood cells following 
occupational exposure (Exs. 5-12; 35-294; 35-84).
    Evidence indicates that even chromates encapsulated in a paint 
matrix may be released in the lungs (Ex. 31-15, p. 2). In a study of 
chromates in aircraft spray paint, LaPuma et al. measured the mass of 
Cr(VI) released from particles into water originating from three types 
of paint particles: solvent-borne epoxy (25% strontium chromate 
(SrCrO4)), water-borne epoxy (30% SrCrO4) and 
polyurethane (20% SrCrO4) (Ex. 31-2-1). The mean fraction of 
Cr(VI) released into the water after one and 24 hours for each primer 
averaged: 70% and 85% (solvent epoxy), 74% and 84% (water epoxy), and 
94% and 95% (polyurethane). Correlations between particle size and the 
fraction of Cr(VI) released indicated that smaller particles (< 5 [mu]m) 
release a larger fraction of Cr(VI) versus larger particles (>5 [mu]m). 
This study demonstrates that the paint matrix only modestly hinders 
Cr(VI) release into a fluid, especially with smaller particles. Larger 
particles, which contain the majority of Cr(VI) due to their size, 
appear to release proportionally less Cr(VI) (as a percent of total 
Cr(VI)) than smaller particles. Some commenters suggested that the 
above research shows that the slightly soluble Cr(VI) from aircraft 
spray paint is less likely to reach and be absorbed in the 
bronchoalveolar region of the lung than a highly soluble Cr(VI) form, 
such as chromic acid aerosol (Exs. 38-106-2; 39-43, 44-33). This issue 
is further discussed in the Carcinogenic Effects Conclusion Section 
V.B.9.a and in the Quantitative Risk Assessment Section VI.G.4.a.
    A number of questions remain unanswered regarding encapsulated 
Cr(VI) and bioavailability from the lung. There is a lack of detailed 
information on the efficiency of encapsulation and whether all of the 
chromate molecules are encapsulated. The stability of the encapsulated 
product in physiological and environmental conditions over time has not 
been demonstrated. Finally, the fate of inhaled encapsulated Cr(VI) in 
the respiratory tract and the extent of distribution in systemic 
tissues has not been thoroughly studied.
3. Dermal Absorption of Cr(VI)
    Both human and animal studies demonstrate that Cr(VI) compounds are 
absorbed after dermal exposure. Dermal absorption depends on the 
oxidation state of chromium, the vehicle and the integrity of the skin. 
Cr(VI) readily traverses the epidermis to the dermis (Exs. 9-49; 309). 
The histological distribution of Cr(VI) within intact human skin was 
studied by Liden and Lundberg (Ex. 35-80). They applied test solutions 
of potassium dichromate in petrolatum or in water as occluded circular 
patches of filter paper to the skin. Results with potassium dichromate 
in water revealed that Cr(VI) penetrated beyond the dermis and 
penetration reached steady state with resorption by the lymph and blood 
vessels by 5 hours. About 10 times more chromium penetrated when 
potassium dichromate was applied in petrolatum than when applied in 
water, indicating that organic solvents facilitate the absorption of 
Cr(VI) from the skin. Research by Baranowska-Dutkiewicz also 
demonstrated that the absorption rates of sodium chromate solutions 
from the occluded forearm skin of volunteers increase with increasing 
concentration (Ex. 35-75). The rates were 1.1 [mu]g Cr(VI)/cm\2\/hour 
for a 0.01 molar solution, 6.4 [mu]g Cr(VI)/cm\2\/hour for a 0.1 molar 
solution, and 10 [mu]g Cr(VI)/cm\2\/hour for a 0.2 molar solution.
    Additional studies have demonstrated that the absorption of Cr(VI) 
compounds can take place through the dermal route. Using volunteers, 
Mali found that potassium dichromate penetrates the intact epidermis 
(Exs. 9-49; 35-41). Wahlberg and Skog demonstrated the presence of 
chromium in the blood, spleen, bone marrow, lymph glands, urine and 
kidneys of guinea pigs dermally exposed to \51\chromium labeled Cr(VI) 
compounds (Ex. 35-81).
4. Absorption of Cr(VI) by the Oral Route
    Inhaled Cr(VI) can enter the digestive tract as a result of 
mucocilliary clearance and swallowing. Studies indicate Cr(VI) is 
absorbed from the gastrointestinal tract. For example, in a study by 
Donaldson and Barreras, the six-day fecal and 24-hour urinary excretion 
patterns of radioactivity in groups of six volunteers given Cr(VI) as 
sodium chromate labeled with \51\chromium indicated that at least 2.1% 
of the Cr(VI) was absorbed. After intraduodenal administration at least 
10% of the Cr(VI) compound was absorbed. These studies also 
demonstrated that Cr(VI) compounds are reduced to Cr(III) compounds in 
the stomach, thereby accounting for the relatively poor 
gastrointestinal absorption of orally administered Cr(VI) compounds 
(Exs. 35-96; 35-41). In the gastrointestinal tract, Cr(VI) can be 
reduced to Cr(III) by gastric juices, which is then poorly absorbed 
(Underwood, 1971 as cited in Ex. 19-1; Ex. 35-85).
    In a study conducted by Clapp et al., treatment of rats by gavage 
with an unencapsulated lead chromate pigment or with a silica-
encapsulated lead chromate pigment resulted in no measurable blood 
levels of chromium (measured as Cr(III), detection limit = 10 [mu]g/L) 
after two or four weeks of treatment or after a two-week recovery 
period. However, kidney levels of chromium (measured as Cr(III)) were 
significantly higher in the rats that received the unencapsulated 
pigment when compared to the rats that received the encapsulated 
pigment, indicating that silica encapsulation may reduce the 
gastrointestinal bioavailability of chromium from lead chromate 
pigments (Ex. 11-5). This study does not address the bioavailability of 
encapsulated chromate pigments from the lung where residence time could 
be different.

[[Page 10110]]

5. Distribution of Cr(VI) in the Body
    Once in the bloodstream, Cr(VI) is taken up into erythrocytes, 
where it is reduced to lower oxidation states and forms chromium 
protein complexes during reduction (Ex. 35-41). Once complexed with 
protein, chromium cannot leave the cell and chromium ions are unable to 
repenetrate the membrane and move back into the plasma (Exs. 7-6; 7-7; 
19-1; 35-41; 35-52). Once inside the blood cell, the intracellular 
Cr(VI) reduction to Cr(III) depletes Cr(VI) concentration in the red 
blood cell (Ex. 35-89). This serves to enhance diffusion of Cr(VI) from 
the plasma into the erythrocyte resulting in very low plasma levels of 
Cr(VI). It is also believed that the rate of uptake of Cr(VI) by red 
blood cells may not exceed the rate at which they reduce Cr(VI) to 
Cr(III) (Ex. 35-99). The higher tissue levels of chromium after 
administration of Cr(VI) than after administration of Cr(III) reflect 
the greater tendency of Cr(VI) to traverse plasma membranes and bind to 
intracellular proteins in the various tissues, which may explain the 
greater degree of toxicity associated with Cr(VI) (MacKenzie et al. 
1958 as cited in 35-52; Maruyama 1982 as cited in 35-41; Ex. 35-71).
    Examination of autopsy tissues from chromate workers who were 
occupationally exposed to Cr(VI) showed that the highest chromium 
levels were in the lungs. The liver, bladder, and bone also had 
chromium levels above background. Mancuso examined tissues from three 
individuals with lung cancer who were exposed to chromium in the 
workplace (Ex. 124). One was employed for 15 years as a welder, the 
second and third worked for 10.2 years and 31.8 years, respectively, in 
ore milling and preparations and boiler operations. The cumulative 
chromium exposures for the three workers were estimated to be 3.45, 
4.59, and 11.38 mg/m\3\-years, respectively. Tissues from the first 
worker were analyzed 3.5 years after last exposure, the second worker 
18 years after last exposure, and the third worker 0.6 years after last 
exposure. All tissues from the three workers had elevated levels of 
chromium, with the possible exception of neural tissues. Levels were 
orders of magnitude higher in the lungs when compared to other tissues. 
Similar results were also reported in autopsy studies of people who may 
have been exposed to chromium in the workplace as well as chrome 
platers and chromate refining workers (Exs. 35-92; 21-1; 35-74; 35-88).
    Animal studies have shown similar distribution patterns after 
inhalation exposure. For example, a study by Baetjer et al. 
investigated the distribution of Cr(VI) in guinea pigs after 
intratracheal instillation of slightly soluble potassium dichromate 
(Ex. 7-8). At 24 hours after instillation, 11% of the original dose of 
chromium from potassium dichromate remained in the lungs, 8% in the 
erythrocytes, 1% in plasma, 3% in the kidney, and 4% in the liver. The 
muscle, skin, and adrenal glands contained only a trace. All tissue 
concentrations of chromium declined to low or nondetectable levels in 
140 days, with the exception of the lungs and spleen.
6. Metabolic Reduction of Cr(VI)
    Cr(VI) is reduced to Cr(III) in the lungs by a variety of reducing 
agents. This serves to limit uptake into lung cells and absorption into 
the bloodstream. Cr(V) and Cr(IV) are transient intermediates in this 
process. The genotoxic effects produced by the Cr(VI) are related to 
the reduction process and are further discussed in the section V.B.8 on 
Mechanistic Considerations.
    In vivo and in vitro experiments in rats indicated that, in the 
lungs, Cr(VI) can be reduced to Cr(III) by ascorbate and glutathione. A 
study by Suzuki and Fukuda showed that the reduction of Cr(VI) by 
glutathione is slower than the reduction by ascorbate (Ex. 35-65). 
Other studies have reported the reduction of Cr(VI) to Cr(III) by 
epithelial lining fluid (ELF) obtained from the lungs of 15 individuals 
by bronchial lavage. The average overall reduction capacity was 0.6 
[mu]g Cr(VI)/mg of ELF protein. In addition, cell extracts made from 
pulmonary alveolar macrophages derived from five healthy male 
volunteers were able to reduce an average of 4.8 [mu]g Cr(VI)/10\6\ 
cells or 14.4 [mu]g Cr(VI)/mg protein (Ex. 35-83). Postmitochondrial 
(S12) preparations of human lung cells (peripheral lung parenchyma and 
bronchial preparations) were also able to reduce Cr(VI) to Cr(III) (De 
Flora et al. 1984 as cited in Ex. 35-41).
7. Elimination of Cr(VI) From the Body
    Excretion of chromium from Cr(VI) compounds is predominantly in the 
urine, although there is some biliary excretion into the feces. In both 
urine and feces, the chromium is present as low molecular weight 
Cr(III) complexes. Absorbed chromium is excreted from the body in a 
rapid phase representing clearance from the blood and at least two 
slower phases representing clearance from tissues. Urinary excretion 
accounts for over 50% of eliminated chromium (Ex. 35-41). Although 
chromium is excreted in urine and feces, the intestine plays only a 
minor part in chromium elimination, representing only about 5% of 
elimination from the blood (Ex. 19-1). Normal urinary levels of 
chromium in humans have been reported to range from 0.24-1.8 [mu]g/L 
with a median level of 0.4 [mu]g/L (Ex. 35-79). Humans exposed to 0.01-
0.1 mg Cr(VI)/m\3\ as potassium dichromate (8-hour time-weighted 
average) had urinary excretion levels from 0.0247 to 0.037 mg Cr(III)/
L. Workers exposed mainly to Cr(VI) compounds had higher urinary 
chromium levels than workers exposed primarily to Cr(III) compounds. An 
analysis of the urine did not detect Cr(VI), indicating that Cr(VI) was 
rapidly reduced before excretion (Exs. 35-294; 5-48).
    A half-life of 15-41 hours has been estimated for chromium in urine 
for four welders using a linear one-compartment kinetic model (Exs. 35-
73; 5-52; 5-53). Limited work on modeling the absorption and deposition 
of chromium indicates that adipose and muscle tissue retain chromium at 
a moderate level for about two weeks, while the liver and spleen store 
chromium for up to 12 months. The estimated half-life for whole body 
chromium retention is 22 days for Cr(VI) (Ex. 19-1). The half-life of 
chromium in the human lung is 616 days, which is similar to the half-
life in rats (Ex. 7-5).
    Elimination of chromium was shown to be very slow in rats exposed 
to 2.1 mg Cr(VI)/m\3\ as zinc chromate six hours/day for four days. 
Urinary levels of chromium remained almost constant for four days after 
exposure and then decreased (Ex. 35-93). After intratracheal 
administration of sodium dichromate to rats, peak urinary chromium 
concentrations were observed at six hours, after which the urinary 
concentrations declined rapidly (Ex. 35-94). The more prolonged 
elimination of the moderately soluble zinc chromate as compared to the 
more soluble sodium dichromate is consistent with the influence of 
Cr(VI) solubility on absorption from the respiratory tract discussed 
earlier.
    Information regarding the excretion of chromium in humans after 
dermal exposure to chromium or its compounds is limited. Fourteen days 
after application of a salve containing water soluble potassium 
chromate, which resulted in skin necrosis and sloughing at the 
application site, chromium was found at 8 mg/L in the urine and 0.61 
mg/100 g in the feces of one individual (Brieger 1920 as cited in Ex. 
19-1). A slight increase over background levels of urinary chromium was 
observed in four

[[Page 10111]]

subjects submersed in a tub of chlorinated water containing 22 mg 
Cr(VI)/L as potassium dichromate for three hours (Ex. 31-22-6). For 
three of the four subjects, the increase in urinary chromium excretion 
was less than 1 [mu]g/day over the five-day collection period. Chromium 
was detected in the urine of guinea pigs after radiolabeled sodium 
chromate solution was applied to the skin (Ex. 35-81).
8. Physiologically-Based Pharmacokinetic Modeling
    Physiologically-based pharmacokinetic (PBPK) models have been 
developed that simulate absorption, distribution, metabolism, and 
excretion of Cr(VI) and Cr(III) compounds in humans (Ex. 35-95) and 
rats (Exs. 35-86; 35-70). The original model (Ex. 35-86) evolved from a 
similar model for lead, and contained compartments for the lung, GI 
tract, skin, blood, liver, kidney, bone, well-perfused tissues, and 
slowly perfused tissues. The model was refined to include two lung 
subcompartments for chromium, one of which allowed inhaled chromium to 
enter the blood and GI tract and the other only allowed chromium to 
enter the GI tract (Ex. 35-70). Reduction of Cr(VI) to Cr(III) was 
considered to occur in every tissue compartment except bone.
    The model was developed from several data sets in which rats were 
dosed with Cr(VI) or Cr(III) intravenously, orally or by intratracheal 
instillation, because different distribution and excretion patterns 
occur depending on the route of administration. In most cases, the 
model parameters (e.g., tissue partitioning, absorption, reduction 
rates) were estimated by fitting model simulations to experimental 
data. The optimized rat model was validated against the 1978 Langard 
inhalation study (Ex. 35-93). Chromium blood levels were overpredicted 
during the four-day inhalation exposure period, but blood levels during 
the post-exposure period were well predicted by the model. The model-
predicted levels of liver chromium were high, but other tissue levels 
were closely estimated.
    A human PBPK model recently developed by O'Flaherty et al. is able 
to predict tissue levels from ingestion of Cr(VI) (Ex. 35-95). The 
model incorporates differential oral absorption of Cr(VI) and Cr(III), 
rapid reduction of Cr(VI) to Cr(III) in major body fluids and tissues, 
and concentration-dependent urinary clearance. The model does not 
include a physiologic lung compartment, but can be used to estimate an 
upper limit on pulmonary absorption of inhaled chromium. The model was 
calibrated against blood and urine chromium concentration data from a 
group of controlled studies in which adult human volunteers drank 
solutions of soluble Cr(III) or Cr(VI).
    PBPK models are increasingly used in risk assessments, primarily to 
predict the concentration of a potentially toxic chemical that will be 
delivered to any given target tissue following various combinations of 
route, dose level, and test species. Further development of the 
respiratory tract portion of the model, specific Cr(VI) rate data on 
extracellular reduction and uptake into lung cells, and more precise 
understanding of critical pathways inside target cells would improve 
the model value for risk assessment purposes.
9. Summary
    Based on the studies presented above, evidence exists in the 
literature that shows Cr(VI) can be systemically absorbed by the 
respiratory tract. The absorption of inhaled chromium compounds depends 
on a number of factors, including physical and chemical properties of 
the particles (oxidation state, size, and solubility), the reduction 
capacity of the ELF and alveolar macrophages and clearance by the 
mucocliary escalator and phagocytosis. Highly water soluble Cr(VI) 
compounds (e.g. sodium chromate) enter the bloodstream more readily 
than highly insoluble Cr(VI) compounds (e.g. lead chromate). However, 
insoluble compounds may have longer residence time in lung. Absorption 
of Cr(VI) can also take place after oral and dermal exposure, 
particularly if the exposures are high.
    The chromate (CrO4) 2- enters cells via 
facilitated diffusion through non-specific anion channels (similar to 
phosphate and sulfate anions). Following absorption of Cr(VI) compounds 
from various exposure routes, chromium is taken up by the blood cells 
and is widely distributed in tissues as Cr(VI). Inside blood cells and 
tissues, Cr(VI) is rapidly reduced to lower oxidation states and bound 
to macromolecules which may result in genotoxic or cytotoxic effects. 
However, in the blood a substantial proportion of Cr(VI) is taken up 
into erythrocytes, where it is reduced to Cr(III) and becomes bound to 
hemoglobin and other proteins.
    Inhaled Cr(VI) is reduced to Cr(III) in vivo by a variety of 
reducing agents. Ascorbate and glutathione in the ELF and macrophages 
have been shown to reduce Cr(VI) to Cr(III) in the lungs. After oral 
exposure, gastric juices are also responsible for reducing Cr(VI) to 
Cr(III). This serves to limit the amount of Cr(VI) systemically 
absorbed.
    Absorbed chromium is excreted from the body in a rapid phase 
representing clearance from the blood and at least two slower phases 
representing clearance from tissues. Urinary excretion is the primary 
route of elimination, accounting for over 50% of eliminated chromium. 
Although chromium is excreted in urine and feces, the intestine plays 
only a minor part in chromium elimination representing only about 5% of 
elimination from the blood.

B. Carcinogenic Effects

    There has been extensive study on the potential for Cr(VI) to cause 
carcinogenic effects, particularly cancer of the lung. OSHA reviewed 
epidemiologic data from several industry sectors including chromate 
production, chromate pigment production, chromium plating, stainless 
steel welding, and ferrochromium production. Supporting evidence from 
animal studies and mechanistic considerations are also evaluated in 
this section.
1. Evidence from Chromate Production Workers
    The epidemiologic literature of workers in the chromate production 
industry represents the earliest and best-documented relationship 
between exposure to chromium and lung cancer. The earliest study of 
chromate production workers in the United States was reported by Machle 
and Gregorius in 1948 (Ex. 7-2). In the United States, two chromate 
production plants, one in Baltimore, MD, and one in Painesville, OH, 
have been the subject of multiple studies. Both plants were included in 
the 1948 Machle and Gregorius study and again in the study conducted by 
the Public Health Service and published in 1953 (Ex. 7-3). Both of 
these studies reported the results in aggregate. The Baltimore chromate 
production plant was studied by Hayes et al. (Ex. 7-14) and more 
recently by Gibb et al. (Ex. 31-22-11). The chromate production plant 
in Painesville, OH, has been followed since the 1950s by Mancuso with 
his most recent follow-up published in 1997. The most recent study of 
the Painesville plant was published by Luippold et al. (Ex. 31-18-4). 
The studies by Gibb and Luippold present historical exposure data for 
the time periods covered by their respective studies. The Gibb exposure 
data are especially interesting since the industrial hygiene data were 
collected on a routine basis and not for compliance purposes. These 
routine air

[[Page 10112]]

measurements may be more representative of those typically encountered 
by the exposed workers. In Great Britain, three plants have been 
studied repeatedly, with reports published between 1952 and 1991. Other 
studies of cohorts in the United States, Germany, Italy and Japan are 
also reported. The elevated lung cancer mortality reported in the great 
majority of these cohorts and the significant upward trends with 
duration of employment and cumulative exposure provide some of the 
strongest evidence that Cr(VI) is carcinogenic to workers. A summary of 
selected human epidemiologic studies in chromate production workers is 
presented in Table V-1.

BILLING CODE 4510-26-P

[[Page 10113]]

[GRAPHIC] [TIFF OMITTED] TR28FE06.002


[[Page 10114]]


[GRAPHIC] [TIFF OMITTED] TR28FE06.003

BILLING CODE 4510-26-C
    The basic hexavalent chromate production process involves milling 
and mixing trivalent chromite ore with soda ash, sometimes in the 
presence of lime (Exs. 7-103; 35-61). The mixture is `roasted' at a 
high temperature, which oxidizes much of the chromite to hexavalent 
sodium chromate. Depending on the lime content used in the process, the 
roast also contains other chromate species, especially calcium

[[Page 10115]]

chromate under high lime conditions. The highly water-soluble sodium 
chromate is water-extracted from the water-insoluble trivalent chromite 
and the less water-soluble chromates (e.g., calcium chromate) in the 
`leaching' process. The sodium chromate leachate is reacted with 
sulfuric acid and sodium bisulfate to form sodium dichromate. The 
sodium dichromate is prepared and packaged as a crystalline powder to 
be sold as final product or sometimes used as the starting material to 
make other chromates such as chromic acid and potassium dichromate.

a. Cohort Studies of the Baltimore Facility. The Hayes et al. study of 
the Baltimore, Maryland chromate production plant was designed to 
determine whether changes in the industrial process at one chromium 
chemical production facility were associated with a decreased risk of 
cancer, particularly cancer of the respiratory system (Ex. 7-14). Four 
thousand two hundred and seventeen (4,217) employees were identified as 
newly employed between January 1, 1945 and December 31, 1974. Excluded 
from this initial enumeration were employees who: (1) were working as 
of 1945, but had been hired prior to 1945 and (2) had been hired since 
1945 but who had previously been employed at the plant. Excluded from 
the final cohort were those employed less than 90 days; women; those 
with unknown length of employment; those with no work history; and 
those of unknown age. The final cohort included 2,101 employees (1,803 
hourly and 298 salaried).
    Hayes divided the production process into three departments: (1) 
The mill and roast or ``dry end'' department which consists of 
grinding, roasting and leaching processes; (2) the bichromate 
department which consists of the acidification and crystallization 
processes; and (3) the special products department which produces 
secondary products including chromic acid. The bichromate and special 
products departments are referred to as the ``wet end''.
    The construction of a new mill and roast and bichromate plant that 
opened during 1950 and 1951 and a new chromic acid and special products 
plant that opened in 1960 were cited by Hayes as ``notable production 
changes'' (Ex. 7-14). The new facilities were designed to ``obtain 
improvements in process technique and in environmental control of 
exposure to chromium bearing dusts * * *'' (Ex. 7-14).
    Plant-related work and health histories were abstracted for each 
employee from plant records. Each job on the employee's work history 
was characterized according to whether the job exposure occurred in (1) 
a newly constructed facility, (2) an old facility, or (3) could not be 
classified as having occurred in the new or the old facility. Those who 
ever worked in an old facility or whose work location(s) could not be 
distinguished based upon job title were considered as having a high or 
questionable exposure. Only those who worked exclusively in the new 
facility were defined for study purposes as ``low exposure''. Data on 
cigarette smoking were abstracted from plant records, but were not 
utilized in any analyses since the investigators thought them ``not to 
be of sufficient quality to allow analysis.''
    One thousand one hundred and sixty nine (1,169) cohort members were 
identified as alive, 494 not individually identified as alive and 438 
as deceased. Death certificates could not be located for 35 reported 
decedents. Deaths were coded to the 8th revision of the International 
Classification of Diseases.
    Mortality analysis was limited to the 1,803 hourly employees 
calculating the standardized mortality ratios (SMRs) for specific 
causes of death. The SMR is a ratio of the number of deaths observed in 
the study population to the number that would be expected if that study 
population had the same specific mortality rate as a standard reference 
population (e.g., age-, gender-, calendar year adjusted U.S. 
population). The SMR is typically multiplied by 100, so a SMR greater 
than 100 represents an elevated mortality in the study cohort relative 
to the reference group. In the Hayes study, the expected number of 
deaths was based upon Baltimore, Maryland male mortality rates 
standardized for age, race and time period. For those where race was 
unknown, the expected numbers were derived from mortality rates for 
whites. Cancer of the trachea, bronchus and lung accounted for 69% of 
the 86 cancer deaths identified and was statistically significantly 
elevated (O=59; E=29.16; SMR=202; 95% CI: 155-263).
    Analysis of lung cancer deaths among hourly workers by year of 
initial employment (1945-1949; 1950-1959 and 1960-1974), exposure 
category (low exposure or questionable/high exposure) and duration of 
employment (short term defined as 90 days-2 years; long term defined as 
3 years +) was also conducted. For those workers characterized as 
having questionable/high exposure, the SMRs were significantly elevated 
for the 1945-1949 and the 1950-1959 hire periods and for both short- 
and long-term workers (not statistically significant for the short-term 
workers initially hired 1945-1949). For those characterized as low 
exposure, there was an elevated SMR for the long-term workers hired 
between 1950 and 1959, but based only on three deaths (not 
statistically significant). No lung cancer cases were observed for 
workers hired 1960-1974.
    Case-control analyses of (1) a history of ever having been employed 
in selected jobs or combinations of jobs or (2) a history of specified 
morbid conditions and combinations of conditions reported on plant 
medical records were conducted. Cases were defined as decedents (both 
hourly and salaried were included in the analyses) whose underlying or 
contributing cause of death was lung cancer. Controls were defined as 
deaths from causes other than malignant or benign tumors. Cases and 
controls were matched on race (white/non-white), year of initial 
employment (+/-3 years), age at time of initial employment (+/-5 years) 
and total duration of employment (90 days-2 years; 3-4 years and 5 
years +). An odds ratio (OR) was determined where the ratio is the odds 
of employment in a job involving Cr(VI) exposure for the cases relative 
to the controls.
    Based upon matched pairs, analysis by job position showed 
significantly elevated odds ratios for special products (OR=2.6) and 
bichromate and special products (OR=3.3). The relative risk for 
bichromate alone was also elevated (OR=2.1, not statistically 
significant).
    The possible association of lung cancer and three health conditions 
(skin ulcers, nasal perforation and dermatitis) as recorded in the 
plant medical records was also assessed. Of the three medical 
conditions, only the odds ratio for dermatitis was statistically 
significant (OR=3.0). When various combinations of the three conditions 
were examined, the odds ratio for having all three conditions was 
statistically significantly elevated (OR=6.0).
    Braver et al. used data from the Hayes study discussed above and 
the results of 555 air samples taken during the period 1945-1950 by the 
Baltimore City Health Department, the U.S. Public Health Service, and 
the companies that owned the plant, in an attempt to examine the 
relationship between exposure to Cr(VI) and the occurrence of lung 
cancer (Ex. 7-17). According to the authors, methods for determining 
the air concentrations of Cr(VI) have changed since the industrial 
hygiene data were collected at the Baltimore plant between 1945 and 
1959. The authors asked the National Institute for Occupational Safety 
and Health (NIOSH) and the Occupational Safety and Health

[[Page 10116]]

Administration (OSHA) to review the available documents on the methods 
of collecting air samples, stability of Cr(VI) in the sampling media 
after collection and the methods of analyzing Cr(VI) that were used to 
collect the samples during that period.
    Air samples were collected by both midget impingers and high volume 
samplers. According to the NIOSH/OSHA review, high volume samplers 
could have led to a ``significant'' loss of Cr(VI) due to the reduction 
of Cr(VI) to Cr(III) by glass or cellulose ester filters, acid 
extraction of the chromate from the filter, or improper storage of 
samples. The midget impinger was ``less subject'' to loss of Cr(VI) 
according to the panel since neither filters nor acid extraction from 
filters was employed. However, if iron was present or if the samples 
were stored for too long, conversion from Cr(VI) to Cr(III) may have 
occurred. The midget impinger can only detect water soluble Cr(VI). The 
authors noted that, according to a 1949 industrial hygiene survey by 
the U.S. Public Health Service, very little water insoluble Cr(VI) was 
found at the Baltimore plant. One NIOSH/OSHA panel member characterized 
midget impinger results as ``reproducible'' and ``accuracy * * * fairly 
solid unless substantial reducing agents (e.g., iron) are present'' 
(Ex. 7-17, p. 370). Based upon the panel's recommendations, the authors 
used the midget impinger results to develop their exposure estimates 
even though the panel concluded that the midget impinger methods ``tend 
toward underestimation'' of Cr(VI).
    The authors also cite other factors related to the industrial 
hygiene data that could have potentially influenced the accuracy of 
their exposure estimates (either overestimating or underestimating the 
exposure). These include: Measurements may have been taken primarily in 
``problem'' areas of the plant; the plants may have been cleaned or 
certain processes shut down prior to industrial hygiene monitoring by 
outside groups; respirator use; and periodic high exposures (due to 
infrequent maintenance operations or failure of exposure control 
equipment) which were not measured and therefore not reflected in the 
available data.
    The authors estimated exposure indices for cohorts rather than for 
specific individuals using hire period (1945-1949 or 1950-1959) and 
duration of exposure, defined as short (at least 90 days but less than 
three years) and long (three years or more). The usual exposure to 
Cr(VI) for both the short- and long-term workers hired 1945-1949 was 
calculated as the average of the mean annual air concentration for 
1945-1947 and 1949 (data were missing for 1948). This was estimated to 
be 413 [mu]g/m3. The usual exposure to Cr(VI) was estimated 
to be 218 [mu]g/m3 for the short and long employees hired 
between 1950 and 1959 based on air measurements in the older facility 
in the early 1950s.
    Cumulative exposure was calculated as the usual exposure level 
times average duration. Short-term workers, regardless of length of 
employment, were assumed to have received 1.6 years of exposure 
regardless of hire period. For long-term workers, the average length of 
exposure was 12.3 years. Those hired 1945-1949 were assigned five years 
at an exposure of 413 [mu]g/m3 and 7.3 years at an exposure 
of 218 [mu]g/m3. For the long-term workers hired between 
1950 and 1959, the average length of exposure was estimated to be 13.4 
years. The authors estimated that the cumulative exposures at which 
``significant increases in lung cancer mortality'' were observed in the 
Hayes study were 0.35, 0.67, 2.93 and 3.65 mg/m3--years. The 
association seen by the authors appears more likely to be the result of 
duration of employment rather than the magnitude of exposure since the 
variation in the latter was small.
    Gibb et al. relied upon the Hayes study to investigate mortality in 
a second cohort of the Baltimore plant (Ex. 31-22-11). The Hayes cohort 
was composed of 1,803 hourly and 298 salaried workers newly employed 
between January 1, 1945 and December 31, 1974. Gibb excluded 734 
workers who began work prior to August 1, 1950 and included 990 workers 
employed after August 1, 1950 who worked less than 90 days, resulting 
in a cohort of 2,357 males followed for the period August 1, 1950 
through December 31, 1992. Fifty-one percent (1,205) of the cohort was 
white; 36% (848) nonwhite. Race was unknown for 13% (304) of the 
cohort. The plant closed in 1985.
    Deaths were coded according to the 8th revision of the 
International Classification of Diseases. Person years of observation 
were calculated from the beginning of employment until death or 
December 31, 1992, whichever came earlier. Smoking data (yes/no) were 
available for 2,137 (93.3%) of the cohort from company records.
    Between 1950 and 1985, approximately 70,000 measurements of 
airborne Cr(VI) were collected utilizing several different sampling 
methods. The program of routine air sampling for Cr(VI) was initiated 
to ``characterize `typical/usual exposures' of workers'' (Ex. 31-22-11, 
p. 117). Area samples were collected during the earlier time periods, 
while both area and personal samples were collected starting in 1977. 
Exposure estimates were derived from the area sampling systems and were 
adjusted to ``an equivalent personal exposure estimate using job-
specific ratios of the mean area and personal sampling exposure 
estimates for the period 1978-1985 * * *'' (Ex. 31-22-11, p. 117). 
According to the author, comparison of the area and personal samples 
showed ``no significant differences'' for about two-thirds of the job 
titles. For several job titles with a ``significant point source of 
contamination'' the area sampling methods ``significantly 
underestimated'' personal exposure estimates and were adjusted ``by the 
ratio of the two'' (Ex. 31-22-11, p. 118).
    A job exposure matrix (JEM) was constructed, where air sampling 
data were available, containing annual average exposure for each job 
title. Data could not be located for the periods 1950-1956 and 1960-
1961. Exposures were modeled for the missing data using the ratio of 
the measured exposure for a job title to the average of all measured 
job titles in the same department. For the time periods where 
``extensive'' data were missing, a simple straight line interpolation 
between years with known exposures was employed.
    To estimate airborne Cr(III) concentrations, 72 composite dust 
samples were collected at or near the fixed site air monitoring 
stations about three years after the facility closed. The dust samples 
were analyzed for Cr(VI) content using ion chromatography. Cr(III) 
content was determined through inductively coupled plasma spectroscopic 
analysis of the residue. The Cr(III):Cr(VI) ratio was calculated for 
each area corresponding to the air sampling zones and the measured 
Cr(VI) air concentration adjusted based on this ratio. Worker exposures 
were calculated for each job title and weighted by the fraction of time 
spent in each air-monitoring zone. The Cr(III):Cr(VI) ratio was derived 
in this manner for each job title based on the distribution of time 
spent in exposure zones in 1978. Cr(VI) exposures in the JEM were 
multiplied by this ratio to estimate Cr(III) exposures.
    Information on smoking was collected at the time of hire for 
approximately 90% of the cohort. Of the 122 lung cancer cases, 116 were 
smokers and four were non smokers at the time of hire. Smoking status 
was unknown for two lung cancer cases. As discussed below, these data 
were used by the study authors to adjust for smoking in their 
proportional hazards regression models used to determine whether lung 
cancer mortality in the worker cohort increased

[[Page 10117]]

with increasing cumulative Cr(VI) exposure.
    A total of 855 observed deaths (472 white; 323 nonwhite and 60 race 
unknown) were reported. SMRs were calculated using U.S. rates for 
overall mortality. Maryland rates (the state in which the plant was 
located) were used to analyze lung cancer mortality in order to better 
account for regional differences in disease fatality. SMRs were not 
adjusted for smoking. In the public hearing, Dr. Gibb explained that it 
was more appropriate to adjust for smoking in the proportional hazards 
models than in the SMRs, because the analyst must make more assumptions 
to adjust the SMRs for smoking than to adjust the regression model (Tr. 
124).
    A statistically significant lung cancer SMR, based on the national 
rate, was found for whites (O=71; SMR=186; 95% CI: 145-234); nonwhites 
(O=47; SMR=188; 95% CI: 138-251) and the total cohort (O=122; SMR=180; 
95% CI: 149-214). The ratio of observed to expected lung cancer deaths 
(O/E) for the entire cohort stratified by race and cumulative exposure 
quartile were computed. Cumulative exposure was lagged five years (only 
exposure occurring five years before a given age was counted). The cut 
point for the quartiles divided the cohort into four equal groups based 
upon their cumulative exposure at the end of their working history (0-
0.00149 mgCrO\3\/m3-yr; 0.0015-0.0089 mgCrO3/m\3\-yr; 0.009-
0.0769 mgCrO3/m\3\-yr; and 0.077-5.25 mgCrO3/
m\3\-yr). For whites, the relative risk of lung cancer was 
significantly elevated for the second through fourth exposure quartiles 
with O/E values of 0.8, 2.1, 2.1 and 1.7 for the four quartiles, 
respectively. For nonwhites, the O/E values by exposure quartiles were 
1.1, 0.9, 1.2 and 2.9, respectively. Only the highest exposure quartile 
was significantly elevated. For the total cohort, a significant 
exposure-response trend was observed such that lung cancer mortality 
increased with increasing cumulative Cr(VI) exposure.
    Proportional hazards models were used to assess the relationship 
between chromium exposure and the risk of lung cancer. The lowest 
exposure quartile was used as the reference group. The median exposure 
in each quartile was used as the measure of cumulative Cr(VI) exposure. 
When smoking status was included in the model, relative lung cancer 
risks of 1.83, 2.48 and 3.32 for the second, third and fourth exposure 
quartiles respectively were estimated. Smoking, Cr(III) exposure, and 
work duration were also significant predictors of lung cancer risk in 
the model.
    The analysis attempted to separate the effects into two 
multivariate proportionate hazards models (one model incorporated the 
log of cumulative Cr(VI) exposure, the log of cumulative Cr(III) 
exposure and smoking; the second incorporated the log of cumulative 
Cr(VI), work duration and smoking). In either regression model, lung 
cancer mortality remained significantly associated (p <  .05) with 
cumulative Cr(VI) exposure even after controlling for the combination 
of smoking and Cr(III) exposure or the combination of smoking and work 
duration. On the other hand, lung cancer mortality was not 
significantly associated with cumulative Cr(III) or work duration in 
the multivariate analysis indicating lung cancer risk was more strongly 
correlated with cumulative Cr(VI) exposure than the other variables.
    Exponent, as part of a larger submission from the Chrome Coalition, 
submitted comments on the Gibb paper prior to the publication of the 
proposed rule. These comments asked that OSHA review methodological 
issues believed by Exponent to impact upon the usefulness of the Gibb 
data in a risk assessment analysis. While Exponent states that the Gibb 
study offers data that ``are substantially better for cancer risk than 
the Mancuso study * * * they believe that further scrutiny of some of 
the methods and analytical procedures is necessary (Ex. 31-18-15-1, p. 
5).
    The issues raised by Exponent and the Chrome Coalition (Ex. 31-18-
14) concerning the Gibb paper are: selection of the appropriate 
reference population for compilation of expected numbers for use in the 
SMR analysis; inclusion of short term workers (<  1 year); expansion of 
the number of exposure groupings to evaluate dose response trends; 
analyzing dose response by peak JEM exposure levels; analyzing dose-
response at exposures above and below the current PEL and calculating 
smoking-adjusted SMRs for use in dose-response assessments. Exponent 
obtained the original data from the Gibb study. The data were 
reanalyzed to address the issues cited above. Exponent's findings are 
presented in Exhibit 31-18-15-1 and are discussed below.
    Exponent suggested that Gibb's use of U.S. and Maryland mortality 
rates for developing expectations for the SMR analysis was 
inappropriate. It suggested that Baltimore city mortality rates would 
have been the appropriate standard to select since those mortality 
rates would more accurately reflect the mortality experience of those 
who worked at the plant. Exponent reran the SMR analysis to compare the 
SMR values reported by Gibb (U.S. mortality rates for SMR analysis) 
with the results of an SMR analysis using Maryland mortality rates and 
Baltimore mortality rates. Gibb reported a lung cancer SMR of 1.86 (95% 
CI: 1.45-2.34) for white males based upon 71 lung cancer deaths using 
U.S. mortality rates. Reanalysis of the data produced a lung cancer SMR 
of 1.85 (95% CI: 1.44-2.33) for white males based on U.S. mortality 
rates, roughly the same value obtained by Gibb. When Maryland and 
Baltimore rates are used, the SMR drops to 1.70 and 1.25 respectively.
    Exponent suggested conducting sensitivity analysis that excludes 
short-term workers (defined as those with one year of employment) since 
the epidemiologic literature suggests that the mortality of short-term 
workers is different than long-term workers. Short-term workers in the 
Gibb study comprise 65% of the cohort and 54% of the lung cancers. The 
Coalition also suggested that data pertaining to short-term employees' 
information are of ``questionable usefulness for assessing the 
increased cancer risk from chronic occupational exposure to Cr(VI)'' 
(Ex. 31-18-15-1, p. 5).
    Lung cancer SMRs were calculated for those who worked for less than 
one year and for those who worked one year or more. Exponent defined 
short-term workers as those who worked less than one year ``because it 
is consistent with the inclusion criteria used by others studying 
chromate chemical production worker cohorts'' (Ex. 31-18-15-1, p. 12). 
Exponent also suggested that Gibb's breakdown of exposure by quartile 
was not the most ``appropriate'' way of assessing dose-response since 
cumulative Cr(VI) exposures remained near zero until the 50th to 60th 
percentile, ``so there was no real distinction between the first two 
quartiles * * * (Ex. 31-18-15-1, p. 24). They also suggested that 
combining ``all workers together at the 75th quartile * * * does not 
properly account for the heterogeneity of exposure in this group'' (Ex. 
31-18-15-1, p. 24). The Exponent reanalysis used six cumulative 
exposure levels of Cr(VI) compared with the four cumulative exposure 
levels of Cr(VI) in the Gibb analysis. The lower levels of exposure 
were combined and ``more homogeneous'' categories were developed for 
the higher exposure levels.
    Using these re-groupings and excluding workers with less than one 
year of employment, Exponent reported that the highest SMRs are seen in 
the highest exposure group (1.5-< 5.25 mg

[[Page 10118]]

CrO3/m\3\-years) for both white and nonwhite, based on 
either the Maryland or the Baltimore mortality rates. The authors did 
not find ``that the inclusion of short-term workers had a significant 
impact on the results, especially if Baltimore rates are used in the 
SMR calculations' (Ex. 31-18-15-1, p. 28).
    Analysis of length of employment and ``peak'' (i.e., highest 
recorded mean annual) exposure level to Cr(VI) was conducted. Exponent 
reported that approximately 50% of the cohort had ``only very low'' 
peak exposure levels (<7.2 [mu]g CrO3/m\3\ or approximately 
3.6 [mu]g/m\3\ of Cr(VI)). The majority of the short-term workers had 
peak exposures of <100 [mu]g CrO3/m\3\. There were five peak 
Cr(VI) exposure levels (<7.2 [mu]g CrO3/m\3\; 7.2-<19.3 
[mu]g CrO3/m\3\; 19.3-<48.0 [mu]g CrO3/m\3\; 
48.0-<105 [mu]g CrO3/m\3\; 105-<182 [mu]g CrO3/
m\3\; and 182-<806 [mu]g CrO3/m\3\) included in the 
analyses. Overall, the lung cancer SMRs for the entire cohort grouped 
according to the six peak exposure categories were slightly higher 
using Maryland reference rates compared to Baltimore reference rates.
    The Exponent analysis of workers who were ever exposed above the 
current PEL versus those never exposed above the current PEL produced 
slightly higher SMRs for those ever exposed, with the SMRs higher using 
the Maryland standard rather than the Baltimore standard. The only 
statistically significant result was for all lung cancer deaths 
combined.
    Assessment was made of the potential impact of smoking on the lung 
cancer SMRs since Gibb did not adjust the SMRs for smoking. Exponent 
stated that the smoking-adjusted SMRs are more appropriate for use in 
the risk assessment than the unadjusted SMRs. It should be noted that 
smoking adjusted SMRs could not be calculated using Baltimore reference 
rates. As noted by the authors, the smoking adjusted SMRs produced 
using Maryland reference rates are, by exposure, ``reasonably 
consistent with the Baltimore-referenced SMRs'' (Ex. 31-18-15-1, p. 
41).
    Gibb et al. included workers regardless of duration of employment, 
and the cohort was heavily weighted by those individuals who worked 
less than 90 days. In an attempt to clarify this issue, Exponent 
produced analyses of short-term workers, particularly with respect to 
exposures. Exponent redefined short-term workers as those who worked 
less than one year, to be consistent with the definition used in other 
studies of chromate producers. OSHA finds this reanalysis excluding 
short-term workers to be useful. It suggests that including cohort 
workers employed less than one year did not substantively alter the 
conclusions of Gibb et al. with regard to the association between 
Cr(VI) exposure and lung cancer mortality. It should be noted that in 
the Hayes study of the Baltimore plant, the cohort is defined as anyone 
who worked 90 days or more.
    Hayes et al. used Baltimore mortality rates while Gibb et al. used 
U.S. mortality rates to calculate expectations for overall SMRs. To 
calculate expectations for the analysis of lung cancer mortality and 
exposure, Gibb et al. used Maryland state mortality rates. The SMR 
analyses provided by Exponent using both Maryland and Baltimore rates 
are useful. The data showed that using Baltimore rates raised the 
expected number of lung cancer deaths and, thus, lowered the SMRs. 
However, there remained a statistically significant increase in lung 
cancer risk among the exposed workers and a significant upward trend 
with cumulative Cr(VI) exposure. The comparison group should be as 
similar as possible with respect to all other factors that may be 
related to the disease except the determinant under study. Since the 
largest portion of the cohort (45%) died in the city of Baltimore, and 
even those whose deaths occurred outside of Baltimore (16%) most likely 
lived in proximity to the city, the use of Baltimore mortality rates as 
an external reference population is preferable.
    Gibb's selection of the cut points for the exposure quartiles was 
accomplished by dividing the workers in the cohort into four equal 
groups based on their cumulative exposure at the end of their working 
history. Using the same method but excluding the short-term workers 
would have resulted in slightly different cumulative exposure 
quartiles. Exponent expressed a preference for a six-tiered exposure 
grouping. The impact of using different exposure groupings is further 
discussed in section VI.C of the quantitative risk assessment.
    The exposure matrix of Gibb et al. utilizes an unusually high-
quality set of industrial hygiene data. Over 70,000 samples taken to 
characterize the ``typical/usual'' working environment is more 
extensive industrial hygiene data then is commonly available for most 
exposure assessments. However, there are several unresolved issues 
regarding the exposure assessment, including the impact of the 
different industrial hygiene sampling techniques used over the sampling 
time frame, how the use of different sampling techniques was taken into 
account in developing the exposure assessment and the use of area vs. 
personal samples.
    Exponent and the Chrome Coalition also suggested that the SMRs 
should have been adjusted for smoking. According to Exponent, smoking 
adjusted SMRs based upon the Maryland mortality rates produced SMRs 
similar to the SMRs obtained using Baltimore mortality rates (Ex. 31-
18-15-1). The accuracy of the smoking data is questionable since it 
represents information obtained at the time of hire. Hayes abstracted 
the smoking data from the plant medical records, but ``found it not to 
be of sufficient quality to allow analysis.'' One advantage to using 
the Baltimore mortality data may be to better control for the potential 
confounding of smoking.
    The Gibb study is one of the better cohort mortality studies of 
workers in the chromium production industry. The quality of the 
available industrial hygiene data and its characterization as 
``typical/usual'' makes the Gibb study particularly useful for risk 
assessment.

b. Cohort Studies of the Painesville Facility. The Ohio Department of 
Health conducted epidemiological and environmental studies at a plant 
in Painesville that manufactured sodium bichromate from chromite ore. 
Mancuso and Hueper (Ex. 7-12) reported an excess of respiratory cancer 
among chromate workers when compared to the county in which the plant 
was located. Among the 33 deaths in males who had worked at the plant 
for a minimum of one year, 18.2% were from respiratory cancer. In 
contrast, the expected frequency of respiratory cancer among males in 
the county in which the plant was located was 1.2%. Although the 
authors did not include a formal statistical comparison, the lung 
cancer mortality rate among the exposed workers would be significantly 
greater than the county rate.
    Mancuso (Ex. 7-11) updated his 1951 study of 332 chromate 
production workers employed during the period 1931-1937. Age adjusted 
mortality rates were calculated by the direct method using the 
distribution of person years by age group for the total chromate 
population as the standard. Vital status follow-up through 1974 found 
173 deaths. Of the 66 cancer deaths, 41 (62.1%) were lung cancers. A 
cluster of lung cancer deaths was observed in workers with 27-36 years 
since first employment.
    Mancuso used industrial hygiene data collected in 1949 to calculate 
weighted average exposures to water-soluble (presumed to be Cr(VI)), 
insoluble (presumed to be principally Cr(III)) and

[[Page 10119]]

total chromium (Ex. 7-98). The age-adjusted lung cancer death rate 
increased from 144.6 (based upon two deaths) to 649.6 (based upon 14 
deaths) per 100,000 in five exposure categories ranging from a low of 
0.25-0.49 to a high of 4.0+ mg/m\3\-years for the insoluble Cr(III) 
exposures. For exposure to soluble Cr(VI), the age adjusted lung cancer 
rates ranged from 80.2 (based upon three deaths) to 998.7 (based upon 
12 deaths) in five exposure categories ranging from < 0.25 to 2.0+ mg/
m\3\-years. For total chromium, the age-adjusted death rates ranged 
from 225.7 (based upon three deaths) to 741.5 (based upon 16 deaths) 
for exposures ranging from 0.50-0.99 mg/m\3\-years to 6.0+ mg/m\3\-
years.
    Age-adjusted lung cancer death rates also were calculated by 
classifying workers by the levels of insoluble Cr(III) and total 
chromium exposure. From the data presented, it appears that for a fixed 
level of insoluble Cr(III), the lung cancer risk appears to increase as 
the total chromium increases (Ex. 7-11).
    Mancuso (Ex. 23) updated the 1975 study. As of December 31, 1993, 
283 (85%) cohort members had died and 49 could not be found. Of the 102 
cancer deaths, 66 were lung cancers. The age-adjusted lung cancer death 
rate per 100,000 ranged from 187.9 (based upon four deaths) to 1,254.1 
(based upon 15 deaths) for insoluble Cr(III) exposure categories 
ranging from 0.25-0.49 to 4.00-5.00 mg/m\3\ years. For the highest 
exposure to insoluble Cr(III) (6.00+ mg/m\3\ years) the age-adjusted 
lung cancer death rate per 100,000 fell slightly to 1,045.5 based upon 
seven deaths.
    The age-adjusted lung cancer death rate per 100,000 ranged from 
99.7 (based upon five deaths) to 2,848.3 (based upon two deaths) for 
soluble Cr(VI) exposure categories ranging from < 0.25 to 4.00+ mg/m\3\ 
years. For total chromium, the age-adjusted lung cancer death rate per 
100,000 ranged from 64.7 (based upon two deaths) to 1,106.7 (based upon 
21 deaths) for exposure categories ranging from < 0.50 to 6.00+ mg/m\3\ 
years.
    To investigate whether the increase in the lung cancer death rate 
was due to one form of chromium compound (presumed insoluble Cr(III) or 
soluble Cr(VI)), age-adjusted lung cancer mortality rates were 
calculated by classifying workers by the levels of exposure to 
insoluble Cr(III) and total chromium. For a fixed level of insoluble 
Cr(III), the lung cancer rate appears to increase as the total chromium 
increases for each of the six total chromium exposure categories, 
except for the 1.00-1.99 mg/m\3\-years category. For the fixed exposure 
categories for total chromium, increasing exposures to levels of 
insoluble Cr(III) showed an increased age-adjusted death rate from lung 
cancer in three of the six total chromium exposure categories.
    For a fixed level of soluble Cr(VI), the lung cancer death rate 
increased as total chromium categories of exposure increased for three 
of the six gradients of soluble Cr(VI). For the fixed exposure 
categories of total chromium, the increasing exposure to specific 
levels of soluble Cr(VI) led to an increase in two of the six total 
chromium exposure categories. Mancuso concluded that the relationship 
of lung cancer is not confined solely to either soluble or insoluble 
chromium. Unfortunately, it is difficult to attribute these findings 
specifically to Cr(III) [as insoluble chromium] and Cr(VI) [as soluble 
chromium] since it is likely that some slightly soluble and insoluble 
Cr(VI) as well as Cr(III) contributed to the insoluble chromium 
measurement.
    Luippold et al. conducted a retrospective cohort study of 493 
former employees of the chromate production plant in Painesville, Ohio 
(Ex. 31-18-4). This Painesville cohort does not overlap with the 
Mancuso cohort and is defined as employees hired beginning in 1940 who 
worked for a minimum of one year at Painesville and did not work at any 
other facility owned by the same company that used or produced Cr(VI). 
An exception to the last criterion was the inclusion of workers who 
subsequently were employed at a company plant in North Carolina (number 
not provided). Four cohort members were identified as female. The 
cohort was followed for the period January 1, 1941 through December 31, 
1997. Thirty-two percent of the cohort worked for 10 or more years.
    Information on potential confounders was limited. Smoking status 
(yes/no) was available for only 35% of the cohort from surveys 
administered between 1960 and 1965 or from employee medical files. For 
those employees where smoking data were available, 78% were smokers 
(responded yes on at least one survey or were identified as smokers 
from the medical file). Information on race also was limited, the death 
certificate being the primary source of information.
    Results of the vital status follow-up were: 303 deaths; 132 
presumed alive and 47 vital status unknown. Deaths were coded to the 
9th revision of the International Classification of Diseases. Cause of 
death could not be located for two decedents. For five decedents the 
cause of death was only available from data collected by Mancuso and 
was recoded from the 7th to the 9th revision of the ICD. There were no 
lung cancer deaths among the five recoded deaths.
    SMRs were calculated based upon two reference populations: The U.S. 
(white males) and the state of Ohio (white males). Lung cancer SMRs 
stratified by year of hire, duration of exposure, time since first 
employment and cumulative exposure group also were calculated.
    Proctor et al. analyzed airborne Cr(VI) levels throughout the 
facility for the years 1943 to 1971 (the plant closed April 1972) from 
800 area air sampling measurements from 21 industrial hygiene surveys 
(Ex. 35-61). A job exposure matrix (JEM) was constructed for 22 
exposure areas for each month of plant operation. Gaps in the matrix 
were completed by computing the arithmetic mean concentration from area 
sampling data, averaged by exposure area over three time periods (1940-
1949; 1950-1959 and 1960-1971) which coincided with process changes at 
the plant (Ex. 31-18-1)
    The production of water-soluble sodium chromate was the primary 
operation at the Painesville plant. It involved a high lime roasting 
process that produced a water insoluble Cr(VI) residue (calcium 
chromate) as byproduct that was transported in open conveyors and 
likely contributed to worker exposure until the conveyors were covered 
during plant renovations in 1949. The average airborne soluble Cr(VI) 
from industrial hygiene surveys in 1943 and 1948 was 0.72 mg/m\3\ with 
considerable variability among departments. During these surveys, the 
authors believe the reported levels may have underestimated total 
Cr(VI) exposure by 20 percent or less for some workers due to the 
presence of insoluble Cr(VI) dust.
    Reductions in Cr(VI) levels over time coincided with improvements 
in the chromate production process. Industrial hygiene surveys over the 
period from 1957 to 1964 revealed average Cr(VI) levels of 270 [mu]g/
m\3\. Another series of plant renovations in the early 1960s lowered 
average Cr(VI) levels to 39 [mu]g/m\3\ over the period from 1965 to 
1972. The highest Cr(VI) concentrations generally occurred in the 
shipping, lime and ash, and filtering operations while the locker 
rooms, laboratory, maintenance shop and outdoor raw liquor storage 
areas had the lowest Cr(VI) levels.
    The average cumulative Cr(VI) exposure (mg/m\3\-yrs) for the cohort 
was 1.58 mg/m\3\-yrs and ranged from 0.006 to 27.8 mg/m\3\-yrs. For 
those who died from lung cancer, the average Cr(VI) exposure was 3.28 
mg/m\3\-yrs and ranged from 0.06 to 27.8 mg/m\3\-yrs.

[[Page 10120]]

According to the authors, 60% of the cohort accumulated an estimated 
Cr(VI) exposure of 1.00 mg/m\3\-yrs or less.
    Sixty-three per cent of the study cohort was reported as deceased 
at the end of the follow-up period (December 31, 1997). There was a 
statistically significant increase for the all causes of death category 
based on both the national and Ohio state standard mortality rates 
(national: O=303; E=225.6; SMR=134; 95% CI: 120-150; state: O=303; 
E=235; SMR=129; 95% CI: 115-144). Fifty-three of the 90 cancer deaths 
were cancers of the respiratory system with 51 coded as lung cancer. 
The SMR for lung cancer is statistically significant using both 
reference populations (national O= 51; E=19; SMR 268; 95% CI: 200-352; 
state O=51; E=21.2; SMR 241; 95% CI: 180-317).
    SMRs also were calculated by year of hire, duration of employment, 
time since first employment and cumulative Cr(VI) exposure, mg/m\3\-
years. The highest lung cancer SMRs were for those hired during the 
earliest time periods. For the period 1940-1949, the lung cancer SMR 
was 326 (O=30; E=9.2; 95% CI: 220-465); for 1950-1959, the lung cancer 
SMR was 275 (O=15; E=5.5; 95% CI: 154-454). For the period 1960-1971, 
the lung cancer SMR was just under 100 based upon six deaths with 6.5 
expected.
    Lung cancer SMRs based upon duration of employment (years) 
increased as duration of employment increased. For those with one to 
four years of employment, the lung cancer SMR was 137 based upon nine 
deaths (E=6.6; 95% CI: 62-260); for five to nine years of employment, 
the lung cancer SMR was 160 (O=8; E=5.0; 95% CI: 69-314). For those 
with 10-19 years of employment, the lung cancer SMR was 169 (O=7; 
E=4.1; 95% CI: 68-349), and for those with 20 or more years of 
employment, the lung cancer SMR was 497 (O=27; E=5.4; 95% CI: 328-723).
    Analyses of cumulative Cr(VI) exposure found the lung cancer SMR 
(based upon the Ohio standard) in the highest exposure group (2.70-
27.80 mg/m\3\-yrs) was 463 (O=20; E=4.3; 95% CI: 183-398). In the 1.05-
2.69 mg/m\3\-yrs cumulative exposure group, the lung cancer SMR was 365 
based upon 16 deaths (E=4.4; 95% CI: 208-592). For the cumulative 
exposure groups 0.49-1.04, 0.20-0.48 and 0.00-0.19, the lung cancer 
SMRs were 91 (O=4; E=4.4; 95% CI: 25-234; 184 (O=8; E=4.4; 95% CI: 79-
362) and 67 (O=3; E=4.5; 95% CI: 14-196). A test for trend showed a 
strong relationship between lung cancer mortality and cumulative Cr(VI) 
exposure (p=0.00002). The authors claim that the SMRs are also 
consistent with a threshold effect since there was no statistically 
significant trend for excess lung cancer mortality with cumulative 
Cr(VI) exposures less than about 1 mg/m\3\-yrs. The issue of whether 
the cumulative Cr(VI) exposure-lung cancer response is best represented 
by a threshold effect is discussed further in preamble section VI on 
the quantitative risk assessment.
    The Painesville cohort is small (482 employees). Excluded from the 
cohort were six employees who worked at other chromate plants after 
Painesville closed. However, exceptions were made for employees who 
subsequently worked at the company's North Carolina plant (number not 
provided) because exposure data were available from the North Carolina 
plant. Subsequent exposure to Cr(VI) by other terminated employees is 
unknown and not taken into account by the investigators. Therefore, the 
extent of the bias introduced is unknown.
    The 10% lost to follow-up (47 employees) in a cohort of this size 
is striking. Four of the forty-seven had ``substantial'' follow-up that 
ended in 1997 just before the end date of the study. For the remaining 
43, most were lost in the 1950s and 1960s (most is not defined). Since 
person-years are truncated at the time individuals are lost to follow 
up, the potential implication of lost person years could impact the 
width of the confidence intervals.
    The authors used U.S. and Ohio mortality rates for the standards to 
compute the expectations for the SMRs, stating that the use of Ohio 
rates minimizes bias that could occur from regional differences in 
mortality. It is unclear why county rates were not used to address the 
differences in regional mortality.
c. Other Cohort Studies. The first study of cancer of the respiratory 
system in the U.S. chromate producing industry was reported by Machle 
and Gregorius (Ex. 7-2). The study involved a total of 11,000 person-
years of observation between 1933 and 1947. There were 193 deaths; 42 
were due to cancer of the respiratory system. The proportion of 
respiratory cancer deaths among chromate workers was compared with 
proportions of respiratory cancer deaths among Metropolitan Life 
Insurance industrial policyholders. A non-significant excess 
respiratory cancer among chromate production workers was found. No 
attempt was made to control for confounding factors (e.g., age). While 
some exposure data are presented, the authors state that one cannot 
associate tumor rates with tasks (and hence specific exposures) because 
of ``shifting of personnel'' and the lack of work history records.
    Baetjer reported the results of a case-control study based upon 
records of two Baltimore hospitals (Ex. 7-7). A history of working with 
chromates was determined from these hospital records and the proportion 
of lung cancer cases determined to have been exposed to chromates was 
compared with the proportion of controls exposed. Of the lung cancer 
cases, 3.4% had worked in a chromate manufacturing plant, while none of 
the controls had such a history recorded in the medical record. The 
results were statistically significant and Baetjer concluded that the 
data confirmed the conclusions reached by Machle and Gregorius that 
``the number of deaths due to cancer of the lung and bronchi is greater 
in the chromate-producing industry than would normally be expected'' 
(Ex. 7-7, p. 516).
    As a part of a larger study carried out by the U.S. Public Health 
Service, the morbidity and mortality of male workers in seven U.S. 
chromate manufacturing plants during the period 1940-1950 was reported 
(Exs. 7-1; 7-3). Nearly 29 times as many deaths from respiratory cancer 
(excluding larynx) were found among workers in the chromate industry 
when compared to mortality rates for the total U.S. for the period 
1940-1948. The lung cancer risk was higher at the younger ages (a 40-
fold risk at ages 15-45; a 30-fold risk at ages 45-54 and a 20-fold 
risk at ages 55-74). Analysis of respiratory cancer deaths (excluding 
larynx) by race showed an observed to expected ratio of 14.29 for white 
males and 80 for nonwhite males.
    Taylor conducted a mortality study in a cohort of 1,212 chromate 
workers followed over a 24 year (1937-1960) period (Ex. 7-5). The 
workers were from three chromate plants that included approximately 70% 
of the total population of U.S. chromate workers in 1937. In addition, 
the plants had been in continuous operation for the study period 
(January 1, 1937 to December 31, 1960). The cohort was followed 
utilizing records of Old Age and Survivors Disability Insurance 
(OASDI). Results were reported both in terms of SMRs and conditional 
probabilities of survival to various ages comparing the mortality 
experience of chromate workers to the U.S. civilian male population. No 
measures of chromate exposure were reported although results are 
provided in terms of duration of employment. Taylor concluded that not 
only was there an excess in mortality from respiratory cancer, but from 
other causes as well, especially as duration of employment increased.

[[Page 10121]]

    In a reanalysis of Taylor's data, Enterline excluded those workers 
born prior to 1889 and analyzed the data by follow-up period using U.S. 
rates (Ex. 7-4). The SMR for respiratory cancer for all time periods 
showed a nine-fold excess (O=69 deaths; E=7.3). Respiratory cancer 
deaths comprised 28% of all deaths. Two of the respiratory cancer 
deaths were malignant neoplasms of the maxillary sinuses, a number 
according to Enterline, ``greatly in excess of that expected based on 
the experience of the U.S. male population.'' Also slightly elevated 
were cancers of the digestive organs (O=16; E=10.4) and non-malignant 
respiratory disease (O=13; E=8.9).
    Pastides et al. conducted a cohort study of workers at a North 
Carolina chromium chemical production facility (Ex. 7-93). Opened in 
1971, this facility is the largest chromium chemical production 
facility in the United States. A low-lime process was used since the 
plant began operation. Three hundred and ninety eight workers employed 
for a minimum of one year between September 4, 1971 and December 31, 
1989 comprised the study cohort. A self-administered employee 
questionnaire was used to collect data concerning medical history, 
smoking, plant work history, previous employment and exposure to other 
potential chemical hazards. Personal air monitoring results for Cr(VI) 
were available from company records for the period February 1974 
through April 1989 for 352 of the 398 cohort members. A job matrix 
utilizing exposure area and calendar year was devised. The exposure 
means from the matrix were linked to each employee's work history to 
produce the individual exposure estimates by multiplying the mean 
Cr(VI) value from the matrix by the duration (time) in a particular 
exposure area (job). Annual values were summed to estimate total 
cumulative exposure.
    Personal air monitoring indicated that TWA Cr(VI) air 
concentrations were generally very low. Roughly half the samples were 
less than 1 [mu]g/m3, about 75 percent were below 3 [mu]g/
m3, and 96 percent were below 25 [mu]g/m3. The 
average worker's age was 42 years and mean duration of employment was 
9.5 years. Two thirds of the workers had accumulated less than 0.01 
[mu]g/m3-yr cumulative Cr(VI) exposure. SMRs were computed 
using National, State (not reported) and county mortality rates (eight 
adjoining North Carolina counties, including the county in which the 
plant is located). Two of the 17 recorded deaths in the cohort were 
from lung cancers. The SMRs for lung cancer were 127 (95% CI: 22-398) 
and 97 (95% CI: 17-306) based on U.S. and North Carolina county 
mortality rates, respectively. The North Carolina cohort is still 
relatively young and not enough time has elapsed to reach any 
conclusions regarding lung cancer risk and Cr(VI) exposure.
    In 2005, Luippold et al. published a study of mortality among two 
cohorts of chromate production workers with low exposures (Ex. 47-24-
2). Luippold et al. studied a total of 617 workers with at least one 
year of employment, including 430 at the North Carolina plant studied 
by Pastides et al. (1994) (``Plant 1'') and 187 hired after the 1980 
institution of exposure-reducing process and work practice changes at a 
second U.S. plant (``Plant 2''). A high-lime process was never used at 
Plant 1, and workers drawn from Plant 2 were hired after the 
institution of a low lime process, so that exposures to calcium 
chromate in both cohorts were likely minimal. Personal air-monitoring 
measures available from 1974 to 1988 for the first plant and from 1981 
to 1998 for the second plant indicated that exposure levels at both 
plants were low, with overall geometric mean concentrations below 1.5 
[mu]g/m3 and area-specific average personal air sampling 
values not exceeding 10 [mu]g/m3 for most years (Ex. 47-24-
2, p. 383).
    Workers were followed through 1998. By the end of follow-up, which 
lasted an average of 20.1 years for workers at Plant 1 and 10.1 years 
at Plant 2, 27 cohort members (4%) were deceased. There was a 41% 
deficit in all-cause mortality when compared to all-cause mortality 
from age-specific state reference rates, suggesting a strong healthy 
worker effect. Lung cancer was 16% lower than expected based on three 
observed vs. 3.59 expected cases, also using age-specific state 
reference rates (Ex. 47-24-2, p. 383). The authors stated that ``[t]he 
absence of an elevated lung cancer risk may be a favorable reflection 
of the postchange environment'', but cautioned that longer follow-up 
allowing an appropriate latency for the entire cohort would be required 
to confirm this conclusion (Ex. 47-24-2, p. 381). OSHA received several 
written testimony regarding this cohort during the post-hearing comment 
period. These are discussed in section VI.B.7 on the quantitative risk 
assessment.
    A study of four chromate producing facilities in New Jersey was 
reported by Rosenman (Ex. 35-104). A total of 3,408 individuals were 
identified from the four facilities over different time periods (plant 
A from 1951-1954; plant B from 1951-1971; plant C from 1937-1964 and 
plant D 1937-1954). No Cr(VI) exposure data was collected for this 
study. Proportionate mortality ratios (PMRs) and proportionate cancer 
mortality ratios (PCMRs), adjusted by race, age, and calendar year, 
were calculated for the three companies (plants A and B are owned by 
one company). Unlike SMRs, PMRs are not based on the expected mortality 
rates in a standardized population but, instead, merely represent the 
proportional distribution of deaths in the cohort relative to the 
general U.S. population. Analyses were done evaluating duration of work 
and latency from first employment.
    Significantly elevated PMRs were seen for lung cancer among white 
males (170 deaths, PMR=1.95; 95% CI: 1.67-2.27) and black males (54 
deaths, PMR=1.88; 95% CI: 1.41-2.45). PMRs were also significantly 
elevated (regardless of race) for those who worked 1-10, 11-20 and >20 
years and consistently higher for white and black workers 11-20 years 
and >20 years since first hire. The results were less consistent for 
those with 10 or fewer years since first hire.
    Bidstrup and Case reported the mortality experience of 723 workers 
at three chromate producing factories in Great Britain (Ex. 7-20). Lung 
cancer mortality was 3.6 times that expected (O=12; E=3.3) for England 
and Wales. Alderson et al. conducted a follow-up of workers from the 
three plants in the U.K. (Bolton, Rutherglen and Eaglescliffe) 
originally studied by Bidstrup (Ex. 7-22). Until the late 1950s, all 
three plants operated a ``high-lime'' process. This process potentially 
produced significant quantities of calcium chromate as a by-product as 
well as the intended sodium dichromate. Process changes occurred during 
the 1940s and 1950s. The major change, according to the author, was the 
introduction of the ``no-lime'' process, which eliminated unwanted 
production of calcium chromate. The no-lime process was introduced at 
Eaglescliffe 1957-1959 and by 1961 all production at the plant was by 
this process. Rutherglen operated a low-lime process from 1957/1959 
until it closed in 1967. Bolton never changed to the low lime process. 
The plant closed in 1966. Subjects were eligible for entry into the 
study if they had received an X-ray examination at work and had been 
employed for a minimum of one year between 1948 and 1977. Of the 3,898 
workers enumerated at the three plants, 2,715 met the cohort entrance 
criteria, (alive: 1,999; deceased: 602; emigrated: 35; and lost to 
follow-up: 79). Those lost to follow-up were not included in the 
analyses. Eaglescliffe contributed the greatest number of subjects to 
the study (1,418). Rutherglen contributed the

[[Page 10122]]

largest number of total deaths (369, or 61%). Lung cancer comprised the 
majority of cancer deaths and was statistically significantly elevated 
for the entire cohort (O=116; E=47.96; SMR= 240; p < 0.001). Two deaths 
from nasal cancer were observed, both from Rutherglen.
    SMRs were computed for Eaglescliffe by duration of employment, 
which was defined based upon plant process updates (those who only 
worked before the plant modification, those who worked both before and 
after the modifications, or those who worked only after the 
modifications were completed). Of the 179 deaths at the Eaglescliffe 
plant, 40 are in the pre-change group; 129 in the pre-/post-change and 
10 in the post-change. A total of 36 lung cancer deaths occurred at the 
plant, in the pre-change group O=7; E=2.3; SMR=303; in the pre-/post-
change group O=27; E=13; SMR=2.03 and in the post-change group O=2; 
E=1.07; SMR=187.
    In an attempt to address several potential confounders, regression 
analysis examined the contributions of various risk factors to lung 
cancer. Duration of employment, duration of follow-up and working 
before or after plant modification appear to be greater risk factors 
for lung cancer, while age at entry or estimated degree of chromate 
exposure had less influence.
    Davies updated the work of Alderson, et al. concerning lung cancer 
in the U.K. chromate producing industry (Ex. 7-99). The study cohort 
included payroll employees who worked a minimum of one year during the 
period January 1, 1950 and June 30, 1976 at any of the three facilities 
(Bolton, Eaglescliffe or Rutherglen). Contract employees were excluded 
unless they later joined the workforce, in which case their contract 
work was taken into account.
    Based upon the date of hire, the workers were assigned to one of 
three groups. The first, or ``early'' group, consists of workers hired 
prior to January 1945 who are considered long term workers, but do not 
comprise