Amicus Curiae Brief — Util. Air Regulatory Grp. v. Envtl. Prot. Agency, 135 S. Ct. 702 (2014) (No. 14-47)
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Supreme Cour, US.
FILED
MAR § - 2015
OFFICE OF THE CLERK
Nos. 14-46, -47, -49
In the Supreme Court of the United States
MICHIGAN, ET AL., PETITIONERS,
.
ENVIRONMENTAL PROTECTION AGENCY, ET AL.,
UTILITY AIR REGULATORY GROUP, PETITIONER,
Vv.
ENVIRONMENTAL PROTECTION AGENCY, ET AL.,
NATIONAL MINING ASSOCIATION, PETITIONER,
Vv.
ENVIRONMENTAL PROTECTION AGENCY, ET AL.,
On Writs of Certiorari To The United States Court
of Appeals For The District of Columbia
BRIEF OF AMICI CURIAE EXPERTS IN AIR
POLLUTION CONTROL AND AIR QUALITY
REGULATION IN SUPPORT OF RESPONDENTS
ELIZABETH J. HUBERTZ
Counsel of Record
INTERDISCIPLINARY ENVIRONMENTAL CLINIC
WASHINGTON UNIVERSITY SCHOOL OF LAW
ONE BROOKINGS DRIVE, CAMPUS Box 1120
ST. LOUIS, MISSOURI 63130
314.935.8760 * ejhubertz@wulaw.wustl.edu
i
TABLE OF CONTENTS
Page
TABLES OF CORTE Beth 2 O vcscceveseosessecsecsasacessnaesincemaasa i
TABLES OF AUTEROIE 8 BIE cesecssesecssisxesacnvessgregnane iv
INTEREST OF THE AMICI CURIAE ....................... 1
SUMMARY OF THE ARGUMENT .....................::::ee 4
PIS IBEN 1 o000s00scsecsevecensosexconsctasacasaensieamener nae 5
I. IN 2000, EPA REASONABLY FOUND IT
APPROPRIATE TO REGULATE EGU HAP
EMISSIONS WITHOUT FORMALLY
CONSIDERING COSTS BECAUSE CONTROL
TECHNOLOGIES FOR REDUCING SUCH
EMISSIONS WERE ALREADY AVAILABLE AND
WIDELY USED, AND THE COSTS OF THOSE
TECHNOLOGIES WERE NOT PROHIBITIVE. ...... 6
A. The HAPs Emitted By EGUs Include Mercury,
Non-Mercury Metals, Acid Gases, And Organic
HAPs; Mercury Has Been Identified As The
HAP Of Greatest Potential Concern For Public
B. Technologies Were Readily Available For
Controlling Mercury And Other HAPs Emitted
By Ue Bae DGD, cnsscnvecsdsscsssciaccee eae 9
i
1. Controls For Non-Mercury Metallic HAPs
And Particle-Bound Mercury ................... 10
2. Controls For Acid Gas HAPs And Ionized
EEE Ee 11
3. Controls For Elemental Mercury............. 14
C. Technologies For Controlling Mercury And
Other HAPs Emitted By EGUs Were Already
SIE EE II, ci dincccedecussvcacconssesccsccsectes 15
1. Installed Base Of Non-Mercury Metallic
HAP And Particle-Bound Mercury
i ac csemnnceanvabavesseoes 16
2. Installed Base Of Acid Gas HAP And
Ionized Mercury Controls......................... 17
3. Installed Base Of Elemental Mercury
i nina ncanencnunncdisucvsenecse 18
D. Because Control Technologies For Reducing
Mercury And Other HAPs Emitted By EGUs
Were Available And Widely Used, And The
Costs Of Those Technologies Were Not
Prohibitive, EPA’s 2000 Finding Was
slain tiadiminapncaestecsesscsecseeeoes 19
1. ESPs And Fabric Filters .......................... 20
2. Flue Gas Desulfurization (Wet/Dry
tae ES Ee 21
il
3. ACI And Other Sorbent Injection
I vic scnscicsanteniteinieibtnisneditediancatdidentedasdomtandiptens 23
Il. EPA REASONABLY AFFIRMED ITS 2000
FINDING THAT REG ULATION WAS
APPROPRIATE BECAUSE COST-EFFECTIVE
EMISSION CONTROL TECHNOLOGIES FOR
MERCURY AND OTHER HAPS WERE IN WIDE
CIEE BS SU: kinscccscteseninssncesitnsmiibinnaninnmanittonsnnaannion 26
A. Between 2000 And 2012, Many EGUs
Installed Mercury Emission Control
Equipment In Response To State
SID: sesisencccnlbsicniiianibiannddcumaiidantdagnaian 27
B. Between 2000 And 2012, Many EGUs
Installed Control Technologies That Will
Reduce Mercury And Other HAP Emissions In
Response To Federal Regulation Of Other
Pollutants And Were Able To Meet The MATS
Requirements Before They Took Effect. ....... 33
ae RIN stirsnerinsctemnseceentetesuaanianéannamiaiananealeinnd 35
iV
TABLE OF AUTHORITIES
Page
STATUTES
PS Oe eT Oe: APNEA 4,8
RROD nee Pore NCS 29
i oda ee 20
abe 8
OTHER AUTHORITIES
AMERICAN LUNG ASSOCIATION, EMISSIONS OF
HAZARDOUS AIR POLLUTANTS FROM COAL-FIRED
POWER PLANTS (Mar. 7, 2011). .................c0ee0ee0es 12, 13
B&W, Southern Co. announce DOE-Based Projects to
Reduce Mercury, INSIDE ENERGY (Dec. 25, 2000),
available at 2000 WL 2108218........................cceeeeees 23
Curtis Carlson, et al., Sulfur Dioxide Control by
Electric Utilities: What Are the Gains from Trade?,
Resources for the Future Discussion Paper ©3-44-
Be CE, Fi iircitiincccanasetcnsnnnsecusaisapanistsisvenginnenanses 22
CLEAN ENERGY GROUP, ENSURING A CLEAN, MODERN
ELECTRIC GENERATING FLEET WHILE MAINTAINING
ELECTRIC SYSTEM RELIABILITY: SUMMER 2011 UPDATE
ID HO sececanss kectenenencabaensacpcudsncumaeinenimecios 28, 29, 32
Vv
DEPARTMENT OF ENERGY/NATIONAL ENERGY
TECHNOLOGY LABORATORY, PHASE II MERCURY
CONTROL TECHNOLOGY FIELD TESTING PROGRAM:
UPDATED ECONOMIC ANALYSIS OF ACTIVATED CARBON
I SEE ra LOD 18-19, 31
ELECTRIC POWER RESEARCH INSTITUTE, FGD
OPTIMIZATION WORKBOOK, available at
http://www.epri.com/abstracts/Pages/ProductAbstract
MARTE TOGUCCIS MT He 1111.26 .........0000cccccccccceccveeceeses 21
ENVIRONMENTAL PROTECTION AGENCY, EPA/600/R-
99/056, COAL UTILITY ENVIRONMENTAL COST
(CUECOosT) WORKBOOK USER’S MANUAL (1999) ...... 21
ENVIRONMENTAL PROTECTION AGENCY, EPA/600/R-
00/093, CONTROLLING SO2 EMISSIONS: A REVIEW OF
TECHNOLOGIES (Nov. 2000)
ENVIRONMENTAL PROTECTION AGENCY, CONTROL OF
MERCURY EMISSIONS FROM COAL-FIRED ELECTRIC
UTILITY BOILERS (Feb. 26, 2004) ........20000..0.000cccceeen 24
ENVIRONMENTAL PROTECTION AGENCY, EPA Sets
National Air Quality Standards (Apr. 30, 1971)
avatlable at http://www?2.epa.gov/aboutepa/epa-sets-
national-air-quality-standards...........................0000 16
ENVIRONMENTAL PROTECTION AGENCY, Mercury
Study Report to Congress (Dec. 1997).......... 21, 22, 31
vl
ENVIRONMENTAL PROTECTION AGENCY, National
Electric Energy Data System (NEEDS) Database
v.3.02, http://www.epa.gov/airmarkets/documents/
ipm/NEEDSV3.02_EISA.xls (Mar. 2002) .... 16, 18, 20
ENVIRONMENTAL PROTECTION AGENCY, National
Electric Energy Data System (NEEDS) Database
v.4.10, http://www.epa.gov/airmarkets/documents/
ipm/NEEDSv410.zip (Apr. 2010)....................... 30, 31
ENVIRONMENTAL PROTECTION AGENCY, Particulate
Matter (PM) Standards — Table of Historical PM
NAAQS, http://www.epa.gov/ttn/naaqs/standards/pm/
Sk LIE SSeS career Pees rer me 16
ENVIRONMENTAL PROTECTION AGENCY, EPA-600/R-
03-110, PERFORMANCE AND COST OF MERCURY AND
MULTIPOLLUTANT EMISSION CONTROL TECHNOLOGY
APPLICATIONS ON ELECTRIC UTILITY BOILERS
ERE RSE eY DIRT are aca eet vara Way 14
ENVIRONMENTAL PROTECTION AGENCY, EPA-600/R-
00-083, PERFORMANCE AND COST OF MERCURY
EMISSION CONTROL TECHNOLOGY APPLICATIONS ON
ELECTRIC UTILITY BOILERS (Sep. 2000).................... 24
ENVIRONMENTAL PROTECTION AGENCY, EPA430-R-99-
011, PROGRESS REPORT ON THE EPA AcID RAIN
rr rr, a ceideueueenaansinnmalennens 18
ENVIRONMENTAL PROTECTION AGENCY, Study of
Hazardous Air Pollutant Emissions from Electric
Utility Steam Generating Units -- Final Report to
IIIS i ccicddimisctagdendecnienchenstumnation 8, 9, 20
vil
ENVIRONMENTAL PROTECTION AGENCY, Sulfur Dioxide
(SOz) Primary Standards — Table of Historical SOz
NAAQS, http://www.epa.gov/ttn/naaqs/standards/so2/
Oe MII is cuicidusdceaicipuminaneictbiniendeniasauaanomiaiates 17
FirstEnergy to Demonstrate Multi-Pollutant Control
System, INDUSTRIAL ENVIRONMENT (July 1, 2000),
available at 2000 WL 9960640........00.00-.....c eee eee 23
LARRY GRAY, REVIEW OF CONTROL TECHNOLOGIES FOR
MERCURY EMISSIONS FROM COAL-FIRED POWER
I I a as a 15
JAMES E. MCCARTHY, CONG. RESEARCH SERV.,
RL33535, MERCURY EMISSIONS FROM ELECTRIC
POWER PLANTS: STATES ARE SETTING STRICTER LIMITS
Memorandum, Mercury Costs Calculations:
Assumptions, Approach, and Results (Sep. 2000),
available at http://www.epa.gov/ttn/atw/combust/
an IAS IE GN Re EPID L RES Pps 25
NATIONAL ASSOCIATION OF CLEAN AIR AGENCIES,
COMMENTS ON Docket ID No. EPA—HQ-—OAR-—2009—
I I i a a a 32
National Emission Standards for Hazardous Air
Pollutants From Coal and Oil-Fired Electric Utility
Steam Generating Units and Standards of
Performance for Fossil-Fuel-Fired Electric Utility,
Industrial-Commercial-Institutional, and Small
Industrial—-Commercial-Institutional Steam
Vill
Generating Units, 77 Fed. Reg. 9.304
a, Gi aaa 6, 27
NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, COMMENTS ON DOCKET ID No. EPA-—
HQ-OAR~2009-0234 (AUG. 2, 2011) ..............00..0060. 32
NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, CONTROL TECHNOLOGIES TO REDUCE
CONVENTIONAL AND HAZARDOUS AIR POLLUTANTS
FROM COAL-FIRED POWER PLANTS
I i i i ar passim
NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, ENVIRONMENTAL REGULATION AND
TECHNOLOGY INNOVATION: CONTROLLING MERCURY
EMISSIONS FROM COAL-FIRED BOILERS
I a aoe ae 22-23, 24
NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, MERCURY EMISSIONS FROM COAL-
FIRED POWER PLANTS (BOUD)....0.ccccscescsccsccevcccccccessce0ss 31
Regulatory Finding on the Emissions of Hazardous
Air Pollutants from Electric Utility Steam
Generating Units, 65 Fed. Reg. 79,825
SI, BI IIE cbccrccnci cukulesicosaansoncsdsbumueccabuineeinaann passim
Revision of December 2000 Regulatory Finding on
the Emissions of Hazardous Air Pollutants From
Electric Utility Steam Generating Units and the
Removal of Coal- and Oil-Fired Electric Utility Steam
Generating Units From the Section 112(c) List, 70
Fed. Reg. 15,994 (Mar. 29, 2005) ..................0cceeeeee 29
1X
Rulemaking To Amend Dates in _ Federal
Implementation Plans Addressing Interstate
Transport of Ozone and Fine Particulate Matter,
ca, @ weet fe |e | eo 27
DAVID G. SLOAT AND PAUL S. FARBER, PARTICULATE
CONTROL FOR INDUSTRIAL APPLICATIONS (Mar. 25,
SEPT nin sc civatacdsacepinasavauudcenueabcbddasaudsainnlanisadciicesadonen es 13
Standards of Performance for New and Existing
Stationary Sources: Electric Utility Steam
Generating Units, Final Rule, 70 Fed. Reg. 28,606
EB, SE cissesidisscissnnnsnntesqdaccontanhstanavatienebsabaciesunios 29
U.S. ENERGY INFO. ADMIN., DOE/EIA-0384(2011),
ANNUAL ENERGY REVIEW 2011 (Sep. 2012), available
at http://www.eia.gov/totalenergy/data/annual/pdf/
ID IIIs saeiinscebn sia oseuaukcwingrces sconunidcavlaidudanentanccseisaumaaeis 24
U.S. ENERGY INFO. ADMIN., Coal-fired power plant
operators consider emissions compliance strategies
(Mar. 28, 2014), http://www.eia.gov/
todayinenergy/detail.cfm?id=15611 ...................0..... 34
U.S. GOov’T ACCOUNTABILITY OFFICE, GAO-10-47,
MERCURY CONTROL TECHNOLOGIES AT COAL-FIRED
POWER PLANTS HAVE ACHIEVED SUBSTANTIAL
EMISSIONS REDUCTION (2009).................ccceceeeeees 30, 32
INTEREST OF THE AMICI CURIAE'!
Amici Curiae are Paul Miller, John Paul, Ranajit
Sahu, and Eric Svenson. The Amici wish to supply
the Court with information § regarding’ the
practicability of reducing hazardous air pollutant
(HAP) emissions from coal-fired electric utility steam
generating units (EGUs) as of 2000, the date of EPA’s
original finding that regulation was appropriate and
necessary. They further explain why in their view,
based on the availability of various. control
technologies for reducing HAP emissions — the costs
of which were reasonably well known and had been
proven to not be prohibitive — it was reasonable for
EPA not to formally consider costs in making this
finding. Amici also wish to provide the Court with an
understanding of the advancements in control
technologies from 2000 to 2012 and how these
advances support EPA’s affirmation of the
appropriate and necessary finding
Amicus Dr. Paul Miller is the Deputy Director
and Chief Scientist of Northeast States for
Coordinated Air Use Management (NESCAUM)
where he provides the organization with legal,
technical, and policy support for all NESCAUM
initiatives. He plays a leading role in supporting
! No counsel for any party had any role in authoring this
brief, and no persons other than the amici curiae and their
counsel made any monetary contribution to its preparation or
submission. Written consents from the parties to the filing of
this brief are on file with the Clerk.
2
state efforts to address acid deposition, mercury
emissions and other air and climate issues. Dr. Miller
has been a Senior Fellow at Princeton University’s
Center for Energy and Environmental Studies, and a
National Research Council Associate at the Joint
Institute for Laboratory Astrophysics, University of
Colorado, Boulder. He has a Ph.D. in Chemical
Physics from Yale University and a J.D. from
Stanford University.
Amicus Mr. John Paul recently retired from his
position as Administrator of the Regional Air
Pollution Control Agency (RAPCA) of Dayton, Ohio.
Mr. Paul worked for the agency from 1973 through
June of 2014 and served as its director from 1985. He
holds a Master of Science from Iowa State University
and a Bachelor of Science from Michigan State
University. Mr. Paul was active in air pollution
control issues in the State of Ohio and nationwide.
He served as co-chair of the National Association of
Clean Air Agencies’ New Source Review Committee,
as well as several terms as an officer and member of
the Board of Directors. He served two six-year terms
on EPA’s Clean Air Act Advisory Committee
(CAAAC) and co-chaired the CAAAC working group
on the utility MACT.
Amicus Dr. Ranajit Sahu is an environmental
engineer and consultant based in Southern
California. Dr. Sahu has more than 25 years of
experience in the fields of environmental, mechanical
and chemical engineering, including: design and
specification of environmental control equipment,
hazardous waste remediation, air pollution control
and equipment’ design, combustion process
engineering, energy studies, multimedia
environmental regulatory compliance, transportation
air quality impact analysis, multipathway health risk
assessments for toxics, air dispersion modeling,
regulatory strategy development, and design for
pollution prevention. He has provided numerous
industrial, government, commercial and _ public
interest group’ clients with comprehensive
multimedia compliance assistance encompassing all
media (air, water, solid and hazardous waste, mixed
waste, noise and community issues). He has Ph.D.
and M.S. degrees in Mechanical Engineering from
the California Institute of Technology and a B.Tech
degree from the Indian Institute of Technology.
Amicus Mr. Eric Svenson is a Senior Advisor with
M.J. Bradley & Associates (MJB&A) where he
focuses on strategic planning and analysis for the
electric and gas utility industry. He has over 39 years
of experience in many aspects of the industry
including: electric power plant operations,
engineering and construction, strategic planning, and
electric and gas transmission and distribution
systems. He also has significant expertise in state,
regional, and federal public policies pertaining to
economic, energy, and environmental regulation.
Prior to joining MJB&A, Eric was the Vice President
for Environment, Health and Safety for Public
Service Enterprise Group, a $16 billion market cap
Fortune 500 electric and gas utility headquartered in
Newark, NJ. He co-chaired EPA’s Greenhouse Gas
Best Available Control Technology (BACT)
committee that provided advice to EPA for its
4
development of BACT regulation and co-authored
with the Natural Resources Defense Council several
reports benchmarking electric power industry
emissions. He holds a Master of Engineering —
Mechanical degree from Stevens Institute of
Technology.
All Amici file this brief solely as individuals and
not on behalf of the institutions with which they are
affiliated.
SUMMARY OF THE ARGUMENT
Fossil fuel-fired power plants account for nearly
seventy percent of electricity generation in the
United States. Coal-fired power plants alone account
for nearly forty percent of total generation. Coal-fired
generation results in emissions of numerous air
pollutants, some of which are toxic and cause or may
cause cancer or other serious health effects. As coal is
burned in utility boilers, mercury and other heavy
metals are released, as are halogens, which form acid
gases such as hydrogen chloride and hydrogen
fluoride. These metals and gases are considered
HAPs under Section 112 of the Clean Air Act.
Based on studies EPA performed and other
information available to it at the time, EPA
concluded in 2000 that it was appropriate and
necessary to regulate HAP emissions from coal- and
oil-fired? EGUs. It based this finding in part on the
* Coal-fired EGUs emit by far the largest amount of utility-
originated HAPs. Oil-fired EGUs contributed to less than two
o
health hazards posed by HAPs emitted by EGUs,
particularly mercury, and on its determination that
when it eventually promulgated a regulation, EGUs
would be able to control their HAP emissions using
technologies that were, for the most part, already
available and already in use at many EGUs in 2000.
In 2012, after an additional decade of experience with
and study of the technological, economic and
operational feasibility of HAP controls, EPA affirmed
its 2000 finding. Both decisions were reasonable and
supported by the facts known to EPA and throughout
the industry.
ARGUMENT
In December 2000, after nearly a decade of study
of the health effects posed by EGU HAP emissions
and the control strategies available to reduce such
emissions, EPA determined that the regulation of
HAPs emitted by coal-fired EGUs was appropriate
and necessary. This decision was based in part on
EPA’s conclusion that technologies for controlling
HAP emissions that posed a threat to the public
health would be available for use (and in some cases
were already in use) once EPA promulgated its
reguiation. More than eleven years later, EPA
affirmed this decision, finding that the control of
EGU HAP emissions was achievable with existing
percent of the total HAP emissions for 1990 and 2010.
Regulatory Finding on the Emissions of Hazardous Air
Pollutants from Electric Utility Steam Generating Units, 65
Fed. Reg. 79,828 (Dec. 20, 2000). Therefore, this brief does not
discuss oil-fired EGUs and focuses solely on coal-fired EGUs.
6
technologies and without placing the reliability of
electric service at risk.
I. IN 2000, EPA REASONABLY FOUND IT
APPROPRIATE TO REGULATE EGU HAP
EMISSIONS WITHOUT FORMALLY
CONSIDERING COSTS BECAUSE CONTROL
TECHNOLOGIES FOR REDUCING SUCH
EMISSIONS WERE ALREADY AVAILABLE
AND WIDELY USED, AND THE COSTS OF
THOSE TECHNOLOGIES WERE NOT
PROHIBITIVE.
A. The HAPs Emitted By EGUs Include
Mercury, Non-Mercury Metals, Acid
Gases, And Organic HAPs; Mercury Has
Been Identified As The HAP Of Greatest
Potential Concern For Public Health.
EGUs emit a variety of HAPs including mercury,
non-mercury metals, acid gases, and organic HAPs.*
3 Organic HAPs include dioxins and furans. The significant
majority of data obtained by EPA for measured organic HAP
emissions from EGUs were below the detection levels of the
EPA test methods, leading EPA to conclude that it is
impracticable to measure organic HAP emissions from EGUs
and to propose work practice standards for organic HAPs
instead of the emission limitations it set for the other HAPs.
National Emission Standards for Hazardous Air Pollutants
From Coal and Oil-Fired Electric Utility Steam Generating
Units and Standards of Performance for Fossil-Fuel-Fired
Electric Utility, Industrial-Commercial-Institutional, and Small
Industrial-Commercial-Institutional Steam Generating Units,
7
Mercury and non-mercury metals (arsenic, cadmium,
chromium, lead, nickel, selenium, and others) are
naturally occurring elements found in coal in trace
amounts. Non-mercury metals generally do not
volatilize (convert into a gaseous state) when coal! is
burned in utility boilers and instead remain as solid
particles or bound to solid particles in the residual
ash. Mercury, by contrast, is highly volatile and
tends to vaporize and become entrained in the flue
gas (combustion exhaust) as either elemental or ionic
mercury vapor. Coal characteristics, e.g., rank,‘ and
combustion conditions dictate which form of vapor
phase mercury predominates. A small amount of
mercury, typically less than 10 percent, does not
volatilize when coal is burned in utility boilers and
remains in the residual ash as particle-bound
mercury.
Coal also contains halogens, highly reactive
elements in a group that includes fluorine, chlorine,
bromine, aud iodine. When coal is burned in utility
boilers the halogens are released and form strong
acids — primarily hydrogen chloride (HCl) and
77 Fed. Reg. 9,369 (Feb. 16, 2012). Therefore, organic HAPs will
not be further discussed in this brief.
‘ Rank is a measure of the degree of alteration that occurs as
buried organic matter undergoing coalification is subjected to
increasing temperature and pressure. Lower rank coals contain
less carbon and have a lower energy content than higher rank
coals. Lower rank coals also generally contain less chlorine,
which oxidizes mercury making it easier to capture in air
pollution control devices. The major ranks, from lowest to
highest, are lignite, subbituminous coal, bituminous coal, and
anthracite.
8
hydrogen fluoride (HF) — as the flue gas cools. The
concentration of halogens in coal varies by coal type,
although chlorine is usually the most abundant.
Coal-fired EGUs emit far more HC] than any other
HAP. EPA, Study of Hazardous Air Pollutant
Emissions from Electric Utility Steam Generating
Units -- Final Report to Congress, Vol. I 3-15 tbl.3-3
(Feb. 1998) (Utility RTC).
Based on the results of the Utility RTC and on
information obtained subsequent to that study,
EPA’s 2000 finding that regulation of EGU HAP
emissions was appropriate identified mercury from
coal-fired EGUs as the HAP of greatest concern for
public health. Regulatory Finding on the Emissions
of Hazardous Air Pollutants from Electric Utility
Steam Generating Units, 65 Fed. Reg. 79,825, 79,826
(Dec. 20, 2000) (2000 Finding). Pursuant to
§112(n)(1) of the Clean Air Act, EPA performed a
study in the late 1990s of the hazards to public
health reasonably anticipated to occur as a result of
EGU HAP emissions after imposition of the other
requirements of the Clean Air Act. EPA examined
HAP emissions test data from 52 coal-, oil-, and
natural gas-fired utility units for the study and
identified 67 of the more than 180 HAPs listed in
Section 112 of the Act as potentially emitted by
EGUs. Utility RTC at ES-2 to ES-4. EPA then
performed an assessment of inhalation and/or
multipathway exposure risks for a subset of priority
HAPs and concluded that mercury from coal-fired
EGUs is the HAP of greatest potential concern for
public health due to its high toxicity, its persistence
in the environment, and its tendency to
9
bioaccumulate in food chains. Jd. at 7-45. EPA also
concluded that arsenic and a few other metals are of
potential concern for carcinogenic effects, and that
dioxins and acid gas HAPs are of potential concern as
well. 2000 Finding at 79,827.
B. Technologies Were Readily Available For
Controlling Mercury And Other HAPs
Emitted By EGUs In 2000.
In 2000, when EPA made its finding that
regulation of EGU HAP emissions was appropriate,
EPA specifically identified a number of strategies for
controlling HAP emissions, including the use of pre-
combustion controls (fuel switching, coal switching,
coal cleaning, coal gasification), combustion controls
(boiler type, low NO, burners), post-combustion
controls (flue gas cleaning technologies), and
alternative controls (demand side management,
energy conservation). Utility RTC at 13-1 to 13-32.
EPA determined that the qualitative effects of these
strategies on EGU HAP emissions varied and could
not be predicted in some cases. Jd. at 13-33. However,
the ability of readily available post-combustion
controls to effectively capture most HAPs emitted by
EGUs was well understood. The available
technologies for controlling particulate matter had
the important co-benefit of capturing metallic HAPs
and particle-bound mercury, while the available
technologies for controlling sulfur dioxide had the
important co-benefit of capturing acid gases and the
ionic form of mercury. In addition, recent data
indicated that post-combustion control of elemental
10
mercury, perhaps the most difficult HAP to capture,
was also possible.
1. Controls For Non-Mercury Metallic
HAPs And Particle-Bound Mercury
Conventional controls for particulate matter (PM)
are highly effective for controlling non-mercury
metallic HAPs. These HAPs normally form or attach
to ash particles and are captured by standard PM
control devices, including electrostatic precipitators
(ESPs) and fabric filters. Mercury bound to ash
particles or other PM is also captured by these
devices.
ESPs use an electrical charge to remove particles
from flue gas under the influence of an electric field.
An ESP imparts a positive or negative charge to
incoming particles, then collects the particles on
oppositely charged plates or tubes. The collection
surfaces are rapped or vibrated periodically to
remove the accumulated particles, which are
collected in a hopper for disposal. ESP effectiveness
depends on the electrical resistivity of the particles
and on particle size. High resistivity particles
(produced by low-sulfur coal) are more difficult to
capture, as are smaller particles. Despite these
difficulties, ESPs can capture more than 99 percent
of total PM and 80 to 95 percent of PMos.°
NORTHEAST STATES FOR COORDINATED AIR USE
5 PMoes, also known as fine particulate matter, consists of
particles 2.5 micrometers in diameter or smaller.
11
MANAGEMENT, CONTROL TECHNOLOGIES TO REDUCE
CONVENTIONAL AND HAZARDOUS AIR POLLUTANTS
FROM COAL-FIRED POWER PLANTS 23 (Mar. 31, 2011)
(2011 NESCAUM Report).
Fabric filters trap and collect particles in flue gas
as it passes through the filter. The filters are made of
woven or felted material in the form of sheets,
cartridges, or bags, although bags are the most
common type. Gas passes freely through fabric
filters, but particles are retained and gradually build
up a cake on the fabric which is periodically removed
by one of a number of different cleaning mechanisms
and collected in a hopper for disposal. Fabric filters
are more efficient than ESPs and can capture up to
99.9 percent of total PM and 99 to 99.8 percent of
PMo2:5. Id. at 24.
ESPs and fabric filters generally capture greater
than 90 percent of all non-mercury metallic HAPs.
2000 Finding at 79,829. Capture rates for particle-
bound mercury are comparable to total PM capture
rates.
2. Controls For Acid Gas HAPs And
Ionized Mercury
Acid gas HAPs (HCl and HF) are effectively
captured by conventional controls for sulfur dioxide
(SOz), a highly reactive gas and criteria pollutant
emitted in large amounts by coal-fired EGUs.
Technologies for capturing SOe are called Flue Gas
12
Desulfurization (FGD) systems and include wet and
dry scrubbers and dry sorbent injection.§
Wet scrubbers inject an aqueous lime or limestone
slurry into the flue gas within a spray tower. SO2 and
acid gases in the flue gas, including HC) and HF, are
absorbed by and react with the alkaline slurry to
produce a wet solid residue, commonly called FGD
sludge, which is then collected for disposal or use as a
by-product. Lime is more reactive than limestone and
offers the potential for higher removal rates but is
also more expensive, so limestone is the most
commonly used reagent. Wet scrubbers typically
capture over 95 percent of SO2 and are sometimes
capable of removal rates in excess of 98 percent.
Removal rates for HCl are even higher. 2011
NESCAUM Report at 10. See also AMERICAN LUNG
ASSOCIATION, EMISSIONS OF HAZARDOUS’ AIR
POLLUTANTS FROM COAL-FIRED POWER PLANTS 32
(Mar. 7, 2011).
Dry scrubbers are similar to wet scrubbers in that
they inject an aqueous lime slurry into the flue gas to
react with acid gases. However, in dry scrubber
systems the slurry has aé_ée higher’ sorbent
concentration, and the water is evaporated by the
heat of the flue gas. As a result, a dry waste product
is formed instead of a wet sludge, which is then
captured in a standard PM control device. Dry
scrubbers are slightly less efficient than wet
¢ A sorbent is a material that collects molecules of another
substance by absorption (drawing molecules into its interstices)
or by adsorption (attracting molecules to its surface).
13
scrubbers but still typically capture more than 90
percent of SOz2. 2011 NESCAUM Report at 11. When
used in conjunction with fabric filters, dry scrubbers
typically capture about 95 percent of HCl. DAviD G.
SLOAT & PAUL S. FARBER, PARTICULATE CONTROL FOR
INDUSTRIAL APPLICATIONS 7 (Mar. 25, 2007).
Dry sorbent injection (DSI) is the pneumatic
injection of a powdered sorbent directly into the
boiler or the downstream ductwork to react with acid
gases in the flue gas. The dry reaction products are
then captured in a standard PM control device.
Capture efficiency depends on the sorbent and the
type of PM control device used. The mineral trona,
the most common sorbent in use, can capture 30-60
percent of SOz when injected upstream of an ESP
and up to 90 percent when injected upstream of a
fabric filter. 2011 NESCAUM Report at 13. EGUs
using DSI with a downstream ESP for particle
collection have demonstrated HCl] captures rates in
the 95-98 percent range. AMERICAN LUNG
ASSOCIATION, EMISSIONS OF HAZARDOUS AIR
POLLUTANTS FROM COAL-FIRED POWER PLANTS 33
(Mar. 7, 2011).
Technologies for SOz and acid gas HAP control
also capture ionic mercury. Ionic mercury vapor is
water-soluble and dissolves in and reacts with the
aqueous slurry used in wet and dry scrubbers. In wet
scrubbers it is collected in the FGD sludge; in dry
scrubbers it is captured in the downstream PM
control device. Removal rates are highly variable and
depend on a number of factors. Wet FGD systems
have exhibited capture rates in the 23 to 97 percent
14
range, while dry FGD systems have exhibited rates
in the 3 to 98 percent range. EPA, EPA-600/R-03-110,
PERFORMANCE AND COST OF MERCURY AND
MULTIPOLLUTANT EMISSION CONTROL TECHNOLOGY
APPLICATIONS ON ELECTRIC UTILITY BOILERS 17-18
(Oct. 2003).
3. Controls For Elemental Mercury
Elemental mercury is insoluble in water and has
poor reactivity with other species so it is not prone to
adsorption onto ash. Approaches for controlling it
include converting it into particle-bound mercury by
means of adsorption onto activated carbon, or
converting it into ionic mercury by adding an
oxidizing agent (e.g., chlorine or bromine) or through
the use of selective catalytic reduction (SCR)
technology.’
Conversion of elemental mercury into particle-
bound mercury is achieved using activated carbon
injection (ACI), which is the pneumatic injection of
powdered activated carbon directly into the flue gas.
Unlike ash, activated carbon particles effectively
adsorb elemental mercury due to their increased
surface area, converting it into particle-bound
mercury and allowing it to be captured in a standard
PM control device. Conversion of elemental mercury
into ionic mercury is achieved by adding a halogen to
7 SCR technology is used to control nitrogen oxides (NQO,).
Flue gas is passed through a catalyst where NO, reacts with the
catalyst and anhydrous ammonia, converting it to nitrogen and
water.
15
the coal or, if ACI is used, to the activated carbon
prior to injection. Halogens help oxidize? elemental
mercury, turning it into ionic mercury which is
captured in FGD systems. SCR technology also
oxidizes elemental mercury for capture in FGD
systems.
EPA was aware of the potential to capture
elemental mercury through the use of sorbents such
as activated carbon at the time of its 2000 finding.
2000 Finding at 79,829. ACI has since been proven
capable of capturing about 65 percent of elemental
mercury using untreated carbon, and in the 90
percent range using carbon treated with chemical
additives. LARRY GRAY, REVIEW OF CONTROL
TECHNOLOGIES FOR MERCURY EMISSIONS FROM COAL-
FIRED POWER PLANTS 8-9 (Oct. 24, 2013).
C. Technologies For Controlling Mercury
And Other HAPs Emitted By EGUs Were
Already Widely Used In 2000.
Technologies for controlling two of the three forms
of mercury and other HAPs emitted by EGUs were
not only available in 2000, when EPA made its
finding that regulation of EGU HAP emissions was
appropriate, they were already widely used. Several
of these technologies had already been in use for
decades by that time.
8 “QOxidize” in this situation refers to the removal of electrons
to make a positively charged mercury ion.
16
1. Installed Base Of Non-Mercury
Metallic HAP And Particle-Bound
Mercury Controls
EPA has regulated some forms of particulate
matter since at least 1971, when the first National
Ambient Air Quality Standards (NAAQS) were
promulgated. EPA, EPA Sets National Air Quality
Standards (Apr. 30, 1971), available at
http://www 2.epa.gov/aboutepa/epa-sets-national-air-
quality-standards. The original PM NAAQS set
limits for total PM. These were replaced in 1987 with
limits for PMio%, and separate limits for PM2s were
added in 1997. EPA, Particulate Matter (PM)
Standards — Table of Historical PM NAAQS,
http://www.epa.gov/ttn/naaqs/standards/pm/s_pm_his
tory.html (last visited Feb. 28, 2015).
For purposes of compliance with the NAAQS and
other Clean Air Act requirements, nearly every EGU
in the U.S. had already installed PM control devices
by 2000, when EPA made its finding. At that time,
300 out of 302 total gigawatts (GW) of coal-fired
capacity (99.2 percent) already had PM controls,
primarily ESPs (256 GW; 84.9 percent) and/or fabric
filters (51 GW; 16.9 percent). EPA, National Electric
Energy Data System (NEEDS) Database v.3.02,
http://www.epa.gov/airmarkets/documents/ipm/NEE
DSV3.02_ EISA.xls (last visited Mar. 2, 2015)
(NEEDS v.3.02). Because these concrol devices have
9 PMho consists of particles 10 micrometers in diameter or
smaller.
17
the co-benefit of capturing metallic HAPs and
particle-bound mercury, the installed base of metallic
HAP/particle-bound mercury controls was also over
99 percent in 2000.
2. Installed Base Of Acid Gas HAP And
Ionized Mercury Controls
Just as the PM NAAQS set limits for that
pollutant, the SOz2 NAAQS have set limits for SO2
since 1971. These limits did not change between 1971
and 2000, except for the revocation of annual and 3-
hour secondary standards in 1973 and 1996,
respectively..° EPA, Sulfur Dioxide (SO2) Primary
Standards — Table of Historical SOz NAAQS,
http://www.epa.gov/ttn/naaqs/standards/so2/s_so2_hi
story.html] (last visited Feb. 28, 2015). Additionally,
in 1990 Congress recognized that SO: pollution was
causing a serious problem that was not being
addressed through the NAAQS -— acid deposition, also
known as acid rain.!! The 1990 Clean Air Act
amendments directed EPA to establish a program to
control acid rain. EPA did so, implementing the Acid
10 Primary NAAQS provide public health protection.
Secondary NAAQS provide public welfare protection, e.¢.,
protection against decreased visibility and damage to animals,
crops, vegetation, and buildings.
11 The presence of acid gases in the air can cause atmospheric
water vapor to shift from a neutral pH to an acidic pH. When
the acidic water vapor condenses, it becomes acid rain, or acid
snow, and can damage trees and other vegetation as well as
cars and buildings. In some cases, the acid gases remain in gas
form or cause dust particles to become acidic. In this form, they
can be inhaled and cause health problems.
18
Rain Program in 1995 which regulated SO2 emissions
from EGUs through a cap-and-trade program. For
purposes of compliance with the NAAQS and other
Clean Air Act requirements and programs, including
the Acid Rain Program, some EGUs — primarily in
the Northeast and the Midwest — had already
installed scrubbers by 2000, when EPA made its
finding. EPA, EPA430-R-99-011, PROGRESS REPORT
ON THE EPA ACID RAIN PROGRAM (Nov. 1999). At
that time, 73 out of 302 total GW of coal-fired
capacity (24 percent) had already installed wet or dry
scrubbers. NEEDS v.3.02. Because these control
devices have the co-benefit of capturing acid gas
HAPs and ionized mercury, the installed base of acid
gas HAP/ionized mercury controls was also 24
percent in 2000.
3. Installed Base Of Elemental Mercury
Controls
Elemental mercury is the only HAP not captured
by controls for other pollutants. However, elemental
mercury can be captured using ACI, which converts
it to particle-bound mercury for capture in PM
control devices, or by adding halogens to the coal (or
to the activated carbon, if ACI is used) to convert it to
ionized mercury for capture in FGD systems. Neither
of these technologies was commercially available
when EPA made its regulatory finding in 2000, but
their theory of operation was well understood, they
had already undergone pilot-scale testing, and full-
scale testing on several coal-fired utility boilers was
approximately one year away. U.S. DEPARTMENT OF
ENERGY, DOE/NETL’S PHASE II MERCURY CONTROL
19
TECHNOLOGY FIELD TESTING PROGRAM: UPDATED
ECONOMIC ANALYSIS Or ACTIVATED CARBON
INJECTION 14 tbl.5 (May 2007) (showing initial
testing at Alabama Power's E.C. Gaston Unit 3 in
April 2001).
D. Because Control Technologies For
Reducing Mercury And Other HAPs
Emitted By EGUs Were Available And
Widely Used, And The Costs Of Those
Technologies Were Not Prohibitive, EPA’s
2000 Finding Was Reasonable.
By the end of 2000, it was apparent that almost
all HAPs, including two of the three species of
mercury, could be removed from EGU emissions
through the use of control devices that also removed
already-regulated criteria pollutants like PM and
SO. as described above. ESPs and fabric filters,
which capture PM, also capture particle-bound
mercury and other metallic HAPs that remain as
particles or bound to solid particles in the residual
ash after coal combustion. See supra Part I.B.
Additionally, scrubbers and DSI, which capture SOz,
also capture acid gas HAPs and ionized mercury from
flue gas. See supra Part L.B.
EPA was not blind to the practical implications of
controlling EGU HAP emissions when it made its
2000 finding that regulation was appropriate. In fact
EPA made its finding based in part on the
technological feasibility of controlling HAP
emissions, coupled with an understanding of the
general expense of mercury and other HAP controls.
20
2000 Finding at 79,828-30 (noting feasibility of
control and technologies that could “greatly reducfe]”
mercury control costs). The general cost of
installation and operation of these control devices
was well known throughout the electric power
generation industry and to EPA. However, the
ultimate cost of emission controls depended heavily
on the degree of removal efficiency that would
eventually be required by regulation after the
completion of the administrative rulemaking
process.'? At the finding stage, EPA’s analysis
demonstrated an understanding of the expense of
control devices relative to the overall costs of EGU
operation, as an inherent aspect of technological
feasibility.
1. ESPs And Fabric Filters
ESPs were the most well-established technology.
At the time of EPA’s finding, they had been used on
boilers for about 80 years. Utility RTC at 2-12.
Similarly, as of 2000, fabric filters had been used on
utility boilers for about two decades, although not on
as wide a scale as ESPs. Id. at 2-13. Of course, not all
installations were the same and they did not involve
the same capital investment or operation costs, but
nonetheless, roughly 99 percent of coal-fired EGU
capacity had installed ESPs, fabric filters or other
PM controls by the end of 1999. NEEDS v.3.02. These
control technologies were in place at a near-universal
12
In fact, Section 112(d)(2) of the Clean Air Act requires this
kind of inquiry at the standard-setting stage for all source
categories, not just EGUs.
21
level and were therefore providing a significant
amount of metallic HAP and particle-bound mercury
control prior to MATS at little additional cost to
operators.'!3 EPA, Mercury Study Report to Congress,
ES-14; Vol. VIII 5-20 (Dec. 1997) (Mercury RTC).
2. Flue Gas Desulfurization (Wet/Dry
Scrubbers)
By 2000, extensive research had been conducted
by EPA and others into the capital and operational
costs of various scrubber configurations that could be
used to remove acid gases and ionized mercury. See,
e.g., EPA, EPA/600/R-00/093, CONTROLLING S02
EMISSIONS: A REVIEW OF TECHNOLOGIES 43-84 (Nov.
2000); Id. at 84 tbl.6-12 (summarizing costs for
various configurations). Industry publications aimed
at EGU operators focused on reducing the costs of
scrubber operation by examining the factors that
could lower the costs of operation, such as age of
equipment, use of different coal types and equipment
selection. EPRI, FGD OPTIMIZATION WORKBOOK, app.
B at 16 tbl.B-8 (Aug. 22, 1998), available at
http://www.epri.com/abstracts/Pages/ProductAbstract
.aspx?ProductId=TR-111118. EPA also offered a tool
for estimating capital and operating costs. See EPA,
EPA/600/R-99/056, COAL UTILITY ENVIRONMENTAL
Cost (CUECOST) WORKBOOK USER’S MANUAL (1999).
Indeed, the basic facts about the conditions most
favorable for scrubber use were well known
13 Some older ESPs might require upgrades or add-on
equipment to enhance efficiency.
22
throughout the power-generation sector. For
example, it was known that wet scrubbers had a
higher efficiency, and that scrubbers generally were
more cost effective on higher capacity generating
units. EPA, EPA/600/R-00/093, CONTROLLING S02
EMISSIONS: A REVIEW OF TECHNOLOGIES 24, 56 (Nov.
2000). It was also well known that acid gas HAP and
mercury removal through the use of SQOz2 control
technology was a co-benefit and, to the extent that
such equipment was already installed, provided acid
gas HAP and ionized mercury control at little
additional cost to operators. Mercury RTC, Vol. VII,
5-20.
Moreover, it was well known that the marginal
cost of SOz abatement, including the cost of
scrubbers, had dropped significantly between 1990
and 2000, due in part to advances in control
technology. Curtis Carlson, et. al., Sulfur Dioxde
Control by Electric Utilities: What Are the Gains from
Trade?, Resources for the Future Discussion Paper
98-44-REV 34 (Apr. 2000) (the marginal abatement
cost of FGD due to technology improvements had
dropped by $50 per ton of SO2). Studies also indicated
that industry had significantly overestimated the
cost of SOz removal during the 1980s and early
1990s. NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, ENVIRONMENTAL REGULATION AND
TECHNOLOGY INNOVATION: CONTROLLING MERCURY
EMISSIONS FROM COAL-FIRED BOILERS V-6 to V-7
23
(Sep. 2000) (2000 NESCAUM Report).'* At any rate,
between 1991 and 1995, 19 GW of U.S. generating
capacity installed scrubbers, bringing the installed
base to about 24 percent of total generating capacity
by 1999.15 See supra Part I.C.2.
2. ACI And Other Sorbent Injection
Systems
Although activated carbon injection and other
controls for elemental mercury were not yet
commercially available in 2000, their theory of
operation was well understood, bench- and pilot-scale
projects had been completed, and _ full-scale
demonstration projects were in the initial stages,
such as the one at FirstEnergy’s Eastlake facility
near Cleveland, Ohio, with more scheduled to follow,
such as the ones at Alabama Power Company’s
Gaston facility and at the Pleasant Prairie plant in
Wisconsin. FirstEnergy to Demonstrate Multi-
Pollutant Control System, INDUSTRIAL ENVIRONMENT
(July 1, 2000), available at 2000 WL 9960640
(demonstration of ECO technology to control
“nitrogen oxide (NO,), sulfur dioxide, fine particulate
matter, mercury and other substances”); B&W,
Southern Co. announce DOE-Based Projects to
‘4 See also 2000 NESCAUM Report at xiv (“early estimates
consistently overstate actual compliance costs, often by a factor
of two or more”).
‘6 This was lower than expected due to the significant drop in
the cost of low-sulfur coal. Burning low-sulfur coal proved a
cheaper e!ternative than installing FGD technology. See 2000
NESCAUM Report at [V-25 to IV-26.
24
Reduce Mercury, INSIDE ENERGY (Dec. 25, 2000),
available at 2000 WL 2108218; EPA, CONTROL OF
MERCURY EMISSIONS FROM COAL-FIRED ELECTRIC
UTILITY BOILERS 4-6 (Feb. 26, 2004).
Using the results of pilot and bench-scale studies
and cost-projection modeling, experts were able to
estimate the cost to EGUs of elemental mercury
removal. According to EPA, the capital costs of
activated carbon technology were relatively low.
EPA, EPA-600/R-00/083, PERFORMANCE AND CosT OF
MERCURY EMISSION CONTROL TECHNOLOGY
APPLICATIONS ON ELECTRIC UTILITY BOILERS 7 (Sep.
2000). The then-best estimate of mercury removal
costs ranged from 0.305 mills per kilowatt-hour at
the low end to 3.783 mills per kilowatt-hour at the
highest,'§ just 0.4 to 4.9 percent of the average retail
price of electricity in 2000.17 The costs of elemental
mercury removal were roughly comparable to the
cost of removing nitrogen oxides. Jd. at 23.'8
16
The use of hot-side ESP technology at a smal] number of
power plants is responsible for the highest numbers. If those
are excluded, the upper end of the range is only 1.915 mills per
kilowatt-hour. Id. at 22-23.
17 On average, consumers paid six to eight cents per kilowatt-
hour for electricity. U.S. ENERGY INFO. ADMIN., DOE/EIA-
0384(2011), ANNUAL ENERGY REVIEW 2011 (Sep. 2012),
available at http://www.eia.gov/totalenergy/data/annual/pdf/
aer.pdf. A mill is Viooo of a dollar.
18 See also 2000 NESCAUM Report at VI-19. Both the EPA
study and the NESCAUM report were part of the
administrative record EPA assembled in conjunction with the
2000 Finding in preparation for the rulemaking. Docket Nos. I-
25
Research indicated that the total costs of mercury
removal vary according to an EGU’s existing
configuration of pollution controls, the type of coal it
burns, and the efficiency of the mercury removal
required. For example, one study showed that a
relatively small EGU producing 100 megawatts of
power, burning low-sulfur bituminous coal, and
equipped with an ESP for controlling PM and ACI
and spray cooling for controlling elemental mercury,
would experience costs ranging from a low of 1.262
mills per kilowatt-hour if only 60 percent of the total
mercury is removed to a high of 2.810 mills per
kilowatt-hour if 90 percent of the total mercury is
removed, just 1.6 to 3.7 percent of the average retail
price of electricity in 2000. Jd. at 11 tbl.3 (showing
ESP-4). To give another example, in September 2000,
EPA looked at the effectiveness of removing mercury,
evaluating two possible regulatory scenarios and a
variety of scrubber/fabric filter/ESP/sorbent injection
configurations. Unsurprisingly, the regulatory
scenario that required larger reductions of mercury
(an 80 percent reduction) cost more than the version
that required lower reductions (60 percent).
Memorandum, Mercury Cost Calculations:
Assumptions, Approach, and Results (Sep. 2000),
available at http://www.epa.gov/ttn/atw/combust/
utiltox/hgmemo.pdf.
In other words, while EPA did not conduct a
formal cost-benefit analysis in connection with its
A-138-40; I-A-143, A-92-55, available at
http://www _.epa.gov/ttn/atw/combust/utiltox/eu_index-
master_121603.pdf.
26
2000 finding that regulation of EGU HAP emissions
was appropriate, it was neither blind nor indifferent
to the practical aspects of compliance with any rule
that it might later promulgate. It was aware of the
control technologies and strategies available, it was
aware of the factors driving costs of installation and
use of those technologies, and it was aware of
technological advances on the horizon that could be
adopted by EGUs in the near future. Regulation was
appropriate because it was practicable and
achievable by the industry without compromising
grid reliability or economic security.
Il. EPA REASONABLY AFFIRMED ITS 2000
FINDING THAT:., REGULATION WAS
APPROPRIATE BECAUSE COST-EFFECTIVE
EMISSION CONTROL TECHNOLOGIES FOR
MERCURY AND OTHER HAPS WERE IN WIDE
USE BY 2012.
By 2012 many EGUs were subject to mercury and
other HAP emission requirements through state
regulations. In the more than 11 years following
EPA’s finding that regulation was appropriate, EGUs
installed emission control technologies in order to
meet state mercury and HAP limits; limits that were
in some cases more stringent than those eventually
promulgated by EPA. In addition, other federal
regulations — such as the EPA rules directed at
interstate air pollution, ozone, and acid rain!9 —
19 The Clean Air Interstate Rule (CAIR) was issued by EPA in
2005. Although it was later invalidated by the D.C. Circuit
Court of Appeals in 2008, it remained in effect during litigation
27
compelled a number of EGUs to install control
technologies for other pollutants that have the co-
benefit of controlling mercury and other HAPs. In all
cases, the EGUs were able to meet regulatory
its 2000 finding that regulation of HAP emissions
A. Between 2000 And 2012, Many EGUs
Installed Mercury Emission Control
Equipment In Response’ To State
Regulations.
EPA was not the only governmental agency to
consider regulation of mercury and other HAPs in
over the Cross-State Air Pollution Rule (CSAPR). CSAPR is now
scheduled to replace CAIR in 2015. 79 Fed. Reg. 71,663. The
NOx SIP Call was issued in 1998 and was designed to contro]
interstate ozone pollution by reducing NO, emissions.
28
the late 1990s-early 2000s. A number of state air
pollution agencies*had been aware of the risks posed
by mercury to human health and the environment
and were looking at implementing state-wide rules.
When EPA made its finding that federal regulation
was appropriate and necessary, some _ states
continued to move forward with their own laws.
The earliest state mercury regulation was adopted
by New Hampshire in 2002, followed by Connecticut
in 2003 and New Jersey in 2004. CLEAN ENERGY
GROUP, ENSURING A CLEAN, MODERN ELECTRIC
GENERATING FLEET WHILE MAINTAINING ELECTRIC
SYSTEM RELIABILITY: SUMMER 2011 UPDATE, app. A
(June 2011). These regulations were based in part on
a policy decision that requiring mercury control
technology was both necessary to protect the public
health and was feasible to implement without risking
the reliability of the state’s electricity grid. See JAMES
E. MCCARTHY, CONG. RESEARCH SERV., RL33535,
MERCURY EMISSIONS FROM ELECTRIC POWER PLANTS:
STATES ARE SETTING STRICTER LIMITS 6 & nn. 9-10
(2006).
New Jersey officials observed, for example, that
municipal solid waste incinerators using fabric filter
control and ACI had achieved 99 percent mercury
control over the last decade. They further stated:
“The USDOE cost analyses indicate that retrofitting
the coal-fired boilers with activated carbon injection
(ACI) and [fabric filters] ... can achieve 90 percent
mercury emission reduction. ACI has a low capitol
(sic) cost. It also has low operating costs if [fabric
filter] technology is used.” Jd. at n.10 (quoting New
29
Jersey Department of Environmental Protection,
Summary of Public Comments and Agency
Responses, Control and Prohibition of Mercury
Emissions, December 6, 2004 New Jersey Register,
pp. 83-84, available at http://www.nj.gov/
dep/rules/adoptions/mercury_rule7-27.pdf).
In 2005, EPA backtracked from its 2000 finding
that regulation of HAP emissions at EGUs was
appropriate and necessary and attempted to renfove
EGUs from the list of regulated sources in Section
112(c) of the Clean Air Act.2° This decision sparked
another round of interest in regulation at the state
level, with ten additional states adopting mercury
regulations in 2006 and 2007.2! After that, another
five states adopted regulations, bringing the total to
eighteen states by the summer of 2011.22 These
eighteen states represent 40 percent of states with
20 Revision of December 2000 Regulatory Finding on the
Emissions of Hazardous Air Pollutants From Electric Utility
Steam Generating Units and the Removal of Coal- and Oil-Fired
Electric Utility Steam Generating Units From the Section
112(c) List, 70 Fed. Reg. 15,994 (Mar. 29, 2005). EPA then
attempted to regulate mercury through section 111 instead.
Standards of Performance for New and Existing Stationary
Sources: Electric Utility Steam Generating Units, Final Rule,
70 Fed. Reg. 28,606 (May 18, 2005). Both regulations were
eventually vacated by the D.C. Circuit.
21 Those states were Delaware, Maryland, Illinois, North
Carolina, Montana, Minnesota, Massachusetts, New York,
Colorado, and Georgia. Clean Energy Group, supra, at App. A.
22 Wisconsin, South Carolina, Michigan, Oregon, and Virginia.
Id.
30
coal-fired EGUs.?3 Collectively, they have established
mercury limits on approximately 96 GW of coal-fired
capacity ~— approximately 30 percent of total
capacity.”4
In the regulated states, EGUs have been able to
achieve mercury emission reductions of 90 percent on
average, using the older technologies for controlling
PM and SO: that also reduce particle-bound and
ionized mercury, as well as making use of the newer
technologies for controlling elemental mercury that
became commercially available after 2000. U 3. GOVT
ACCOUNTABILITY OFFICE, GAQO-10-47, MERCURY
CONTROL TECHNOLOGIES AT COAL-FIRED POWER
PLANTS HAVE ACHIEVED SUBSTANTIAL EMISSIONS
REDUCTION 7 (2009). In particular, ACI, which was in
the pilot-test stage at the end of 2000, matured as a
technology in the first decade of the century. Field
testing from 2001-2002 demonstrated that ACI used
in conjunction with an ESP was capable of capturing
up to 94 percent of the elemental mercury released
during the combustion of bituminous coals and
approximately 65 percent of the mercury released
during the combustion of subbituminous coals. When
used in conjunction with a fabric filter, removal
efficiencies in excess of 90 percent were achieved
while using less sorbent than required to achieve
23. Alaska, Hawaii, Idaho, Rhode Island, and Vermont do not
have any coal-fired EGUs. EPA, National Electric Energy Data
System (NEEDS) Database v.4.10, http://www.epa.gov/
airmarkets/documents/ipm/NEEDSv410.zip (last visited Mar. 2,
2015) (NEEDS v.4.10).
24 Jd.
31
similar efficiencies with an ESP NORTHEAST STATES
FOR COORDINATED AIR USE MANAGEMENT, MERCURY
EMISSIONS FROM COAL-FIRED POWER PLANTS 4-5
fig.4.2 (2003).
In 2002, Salem Harbor Station in Salem,
Massachusetts became the first coal-fired power
plant in the U.S. to utilize ACI, installing it on three
units. NEEDS v.4.10. By 2010, an additional 65 units
had installed or planned to install ACI to meet
current or anticipated mercury emission limits.
At the same time, the cost of ACI fell considerably
relative to earlier estimates. Before 2000, the
estimated costs had relatively large uncertainties
and varied considerably, ranging from $10 million to
$31 million for a large EGU unit.25 Mercury RTC,
Vol. VIII 3-11 tbl.3-5 (Dec. 1997). By 2007, the costs
ranged from $800,000 to $10.3 million while
achieving very high removal efficiencies. U.S.
DEPARTMENT OF ENERGY, DOE/NETL’S PHASE II
MERCURY CONTROL TECHNOLOGY FIELD TESTING
PROGRAM: UPDATED ECONOMIC ANALYSIS OF
ACTIVATED CARBON INJECTION 32 tbl.11, 35 tbl.14, 38°
tbl.17 (May 2007). Such reductions in costs and/or
improvements in efficiency are usually expected as a
new technology takes hold.
26 A large unit has a capacity of 975MW, and a smaller unit
100MW.
26 These figures represent annualized costs based on tests
done over a shorter period.
32
With controls for elemental mercury added to the
existing arsenal of controls, EGUs of differing design,
location, and size, that utilize different coals, found it
possible to achieve state-established mercury
limits.27 In fact, by the trme EPA proposed MATS in
2011, the EGUs in six states were already in
compliance with mercury limits stricter than the
proposed MATS standard. CLEAN ENERGY GROUP,
ENSURING A CLEAN, MODERN ELECTRIC GENERATING
FLEET WHILE MAINTAINING ELECTRIC SYSTEM
RELIABILITY: SUMMER 2011 UPDATE at 3 (June 2011).
The experience of the states that have implemented
mercury rules demonstrates that control of mercury
emissions is possible with available technology and
can be accomplished on a cost-effective basis and
without compromising reliability. See, e.g.,
NORTHEAST STATES FOR COORDINATED AIR USE
MANAGEMENT, COMMENTS ON Docket ID No. EPA—
HQ—OAR-2009-0234 at 5-8 (AUG. 2, 2011)
(discussing experience of NESCAUM _ states);
NATIONAL ASSOCIATION OF CLEAN AIR AGENCIES,
COMMENTS ON DOCKET ID No. EPA—-HQ—OAR-2003-—
0234 (Aug. 4, 2011) (discussing experiences in
regulated states).
27, U.S. GOov’T ACCOUNTABILITY OFFICE, GAO-10-47, MERCURY
CONTROL TECHNOLOGIES AT COAL-FIRED POWER PLANTS HAVE
ACHIEVED SUBSTANTIAL EMISSIONS REDUCTION 8 (2009) (finding
that sorbent injection can be used to reduce mercury emissions
on boiler configurations present at nearly three-fourths of coal-
fired EGUs).
33
B. Between 2000 And 2012, Many EGUs
Installed Control Technologies That Will
Reduce Mercury And Other HAP
Emissions In Response To Federal
Regulation Of Other Pollutants And Were
Able To Meet The MATS Requirements
Before They Took Effect.
MATS was not the only federal regulatory
initiative that affected mercury and HAP emissions
from EGUs. CAIR required the EGUs in 28 states to
limit their own emissions of NOx and SOz if those
emissions would contribute to nonattainment of
NAAQS in another state. The NO, SIP call required
26 states, mostly in the eastern U.S., to submit state
implementation plans that would address the
interstate transport of NOx and the formation of
ozone. The Acid Rain Program, part of the 1990 CAA
amendments, had also created incentives for EGUs to
control SOe, although not to the extent hoped for at
its enactment. While none of these rules addressed
mercury or HAP emissions per se, EGUs installed a
variety of control technologies — including scrubbers
and other FGD technologies — in order to comply with
their requirements.
As a result of the limitations on SO2 and NO,,
between 2000 and 2011, EGUs representing 80 GW
28 The Title IV Acid Rain Program (CAA §§ 401-416) differed
from other EPA regulations because it allowed for SO»
emissions trading, allowing some EGUs to lower their emissions
and obtain allowances or credits which they could then sell to
EGUs that did not lower their emissions to the same degree.
34
of generating capacity (approximately 25 percent of
the U.S. total) installed FGD technology, and EGUs
representing 96 GW _ of generating capacity
(approximately 30 percent of the U.S. total) installed
SCR systems. 2011 NESCAUM Report at 26. These
control technologies had the practical co-benefit of
limiting mercury and other HAPs, in addition to their
primary duties of reducing criteria pollutants.
EGU operators have come to recognize that
mercury and other HAP emission control is
technologically, operationally, and _ financially
feasible. Perhaps the most telling statistic is this: “At
the end of 2012, 64.3 percent of the U.S. coal
generating capacity in the electric power sector
already had the appropriate environmental control
equipment to comply with the MATS” — more than
two years before MATS was scheduled to take effect.
U.S. ENERGY INFO. ADMIN., Coal-fired power plant
operators consider emissions compliance strategies
(Mar. 28, 2014), http://www.eia.gov/
todayinenergy/detail.cfm?id=15611. Factoring in the
additional capacity that already planned to add
control equipment before the compliance deadline,
nearly 70 percent of total coal-fired capacity was
either in compliance with the MATS or already had
plans in place to achieve compliance at the end of
2012. Only a minority still needed to determine how
to comply with MATS — and it had over two years to
do so. Id. This is on-the-ground confirmation that
regulation of HAP emissions at EGUs_ was
appropriate and that EPA’s decision was and
remains reasonable.
35
CONCLUSION
For the foregoing reasons, this Court should
affirm the lower court’s decision.
Respectfully submitted,
Elizabeth J. Hubertz *
Interdisciplinary Environmental Clinic
Washington University School of Law
One Brookings Drive, Campus Box 1120
St. Louis, Missouri 63130
314.935.8760 e ejhubertz@wulaw.wustl.edu
* Counsel of record
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