GCI TECH NOTES©
Volume
17, Number 1
A
Gossman
Consulting,
Inc.
Publication
February, 2012
Commercial
and Industrial Solid Waste Incineration (CISWI)
Cement Kiln MACT Regulations
USEPA 40 CFR Parts 60 and 241 Proposed Rules
Published December 23rd 2011
Portions
adapted from comments prepared in
cooperation with Universal
Cement, LLC.
On September 9, 2010, EPA published
in the
Federal Register a new final
set of Portland Cement MACT limitations for new and existing cement
plants.
On March 21, 2011, EPA
published
in the Federal Register a final rule which establishes MACT emission
limits for
cement kilns that burn solid waste. In
May of last year, GCI published a comparison of these two sets of
limits and
critiqued the differences.
On December 23, 2011, EPA proposed
changes
to the March 21 rule.
Table 1 provides an updated
comparison of the
emission limits for new cement kilns. Comments
on the rule itself then follow.
Table 1 - Limits from 2010/2011 Portland
Cement
MACT Regulations
|
PC MACT |
PC Solid Waste MACT |
December 2011 Proposed |
|
Pollutant |
Normal and Malfunction |
Start-up /Shutdown |
Normal Operations |
Normal Operations |
Cd |
N/A |
N/A |
0.00048 mg/dscm @7% O2 |
0.00082 mg/dscm @7% O2 |
CO |
N/A |
N/A |
90 ppm @7% O2 |
90 (straight kiln) |
PCDD/ PCDF |
0.2 TEQ ng/dscm @7% O2 |
0.2 TEQ ng/dscm (no O2 correction) |
0.0030 TEQ ng/dscm @7% O2 |
0.0036 TEQ ng/dscm @7% O2 |
Pb |
N/A |
N/A |
0.0026 mg/dscm @7% O2 |
0.0043 mg/dscm @7% O2 |
Hg |
21 lb/ |
0.004 mg/dscm (no O2 correction) |
0.0062 mg/dscm @7% O2 |
0.0037 mg/dscm @7% O2 |
NOx |
1.5 lb/ton clinker |
200 ppm @7% O2 |
200 ppm @7% O2 |
|
Particulate |
0.04 lb/ |
0.004 gr/dscf |
2.5 mg/dscm |
8.9 mg/dscm |
The
limits proposed for CISWI cement kilns are now very
close to those established in the Portland Cement MACT rule. This
is not surprising given that cement kiln
emissions are related to raw materials, not fuels.
Why
does EPA see the need for further
subcategorization of cement kilns? The
additional CISWI subcategory increases complexity and uncertainty while
achieving no improvement in environmental stewardship.
A
better approach would be to return cement
kilns that use solid waste fuels to regulation under Portland Cement
MACT.
EPA has spent tax dollars and
limited
resources establishing CISWI limits for cement kilns already covered
under
PCMACT.
Perhaps, rather than
continuing
this duplicative effort, EPA could simply acknowledge the limits are
nearly the
same and save itself the trouble of defending a second rule making.
Section
I(C)(5) of the preamble of the proposed rule (on
page 80461 FR) suggests that startup and shutdown periods are limited
to 4 hours
and 1 hour respectively for at least one subcategory.
This
limitation may be erroneously considered
appropriate for all CISWI combustion systems including cement kilns. While
the definitions of startup and shutdown
in this subpart may be appropriate for incinerators or other devices,
they are
not appropriate for cement kilns. Depending
upon circumstances, a cement kiln startup or shutdown could be measured
in days.
Startup
procedures on a kiln system depend upon the type of
system and the situation (e.g. cold startup or hot startup, etc.). In
general, the system is in startup until an
adequate level of production is reached that is capable of sustaining
the
physical, chemical and thermal process needed to make clinker. EPA
should consider startup to be the time
from when fuel is initially fired until stack oxygen levels drop below
15%.
Shutdown
procedures are likewise system specific, but
shutdown operation would generally be considered the time from the last
fuel
entering the system until the ID fan is stopped.
Section
I(C)(9) of the preamble of the proposed rule (on
page 80463 FR) indicates that the dioxin limit was created using three
times
the laboratory detection limit as the quantitation limit for
measurements.
EPA specifically invited
comments on this
approach in comparison with an alternative provided by a petitioner. The
EPA approach is overly simplistic and
does not take into account all of the factors that are needed to
properly
determine a quantitation limit for dioxins.
Specifically, this approach
does not account for differences in the
quantitation limits for individual dioxin congeners.
It
does not take into account factors that
impact both the detection limit and quantitation limit for actual field
samples
that are subject to interferences and matrix effects, nor does this
approach
take into account the actual stack sampling and subsequent sample
handling
impacts on detection and quantitation limits in the emissions. In
order for EPA to set a scientifically
defensible MACT limit on dioxins, all of these factors must be taken
into
account.
In a
peer reviewed paper by Rigo and Chandler, duplicate
sampling trains were used to calculate the quantitation limit. Rigo and Chandler
found in this study, published by the Journal of Air and Waste
Management[1],
that
the Reference Method Quantitation Limit for PCDD/PCDF TEQ in a
municipal waste
combustor may be as high as 0.51 ng/dscm.
This
value is very similar to the petitioner’s suggested limit of
0.3 ng/dscm TEQ that EPA references on page 80463 FR of the preamble.
EPA
should use such a detection limit value statistically
derived from a large number of actual stack tests on cement kilns which
takes
into account the sampling and matrix effects on the quantitation limit,
rather
than the seemingly arbitrary approach suggested by EPA.
Table
7 to Subpart CCCC of Part 60 and Table 8 to Subpart
DDDD of Part 60 present the same limit for existing and new CISWI
cement plants
for dioxins on a TEQ basis but establish a radically different limit on
a total
dioxin basis.
This result is
counter-intuitive, and may indicate a fundamental problem in the
underlying
calculations and analysis performed to establish these limits. EPA
should reexamine the analysis of the data
for dioxins (both TEQ and total) and explain the discrepancy or clarify
the
limits.
60.2105
sets a limit on CO emissions but not THC emissions.
EPA
has more than 20 years of data on cement
kilns that demonstrate that CO is not a good indicator of combustion
conditions
in cement kilns and cannot be used as a surrogate for organic HAPs. In
fact neither CO nor THC is an indicator of
combustion conditions in the kiln but are impacted directly by the
organics in
the raw materials.
Both the Hazardous
Waste Combustor MACT rule and the Portland Cement MACT rule have
acknowledged
this fact by setting limits on THC instead of CO, since THC is a clear
surrogate for organic HAPs.
In order to
be consistent in its approach to setting MACT limits on cement kilns
(regardless of the MACT category), EPA should set a limit on THC rather
than CO,
just has been done in the Portland Cement MACT rule.
60.2105
establishes limits on lead and cadmium emissions. In
a system with relatively high exit gas
temperatures (such as many incinerator systems), these metals may be
volatile
enough to escape from the system. In
a
cement kiln, however, these metals condense in the lower temperature
regions of
the system and are emitted in the form of particulate.
It is
likely that EPA has sufficient data, gathered in the
context of the Portland cement MACT and hazardous waste combustor MACT
rules,
to demonstrate that emissions of these metals are correlated with
particulate
emissions and are independent of the type of fuel being used. For
this reason, the same logic used for
nonvolatile metals in this rule (and used in promulgating the PC MACT
rule)
that allows the use of particulate as a surrogate for metal HAPs (other
than
mercury) can be applied to lead and cadmium for cement kilns regardless
of the
type of fuel used
60.2105
sets limits on HCl.
It is not clear that EPA has
authority to set limits on HCl for kilns
that are area sources.
60.2110
establishes operating limits on specific emissions
control equipment.
Such limits are
unnecessary in cases where CEMs are used to monitor and maintain
compliance.
In a
kiln system, there are multiple factors in the
operation of the kiln system and air pollution control devices that
impact
emissions of one or more pollutants. Controls
that restrict parameters on an emission control device may
unnecessarily
increase emissions of another pollutant without any corresponding
benefit.
For example, there are
multiple ways to
control NOx
emissions from a cement kiln system. Low
NOx
burners, staged
combustion, raw material mix design and details about how an SNCR
system are
operated all can contribute to changes in NOx
emission levels.
The proposed regulation would
set operating
limits on the SNCR system that would not encourage the use of
alternative
control strategies that could reduce the dependence on the SNCR system
and
thereby reduce emissions of both greenhouse gasses and fine particulate. Similar
situations arise for both SO2
and CO.
EPA should eliminate
requirements
to set process operating limits for emissions that are continuously
monitored
with a CEM, since such limits reduce flexibility without a
corresponding
benefit.
60.2115
establishes a complex and probably lengthy petition
process for using an emissions control technology other than those
listed.
This approach increases
barriers to
innovation and decreases incentives to use innovative and advanced
technologies
to reduce emissions.
Especially for
those systems used to control emissions of pollutants for which a CEM
is used
to determine compliance, this petition process should not be required,
as it
adds to the regulatory burden without a corresponding benefit.
60.2145(j)(3)
indicates that the demonstration of initial compliance
with the mercury limit be performed while the raw mill is on and while
it is
off.
In Table 7 to Subpart CCCC of
Part
60 the mercury limit is stated as a 30 day hourly rolling average. It
is not clear that these requirements are
congruent.
The 30
day hourly rolling average limit for mercury is a
health based limit that also takes into account the natural
fluctuations of
mercury emissions when the raw mill is shut down. Applying
this limit to a shorter time period
while the raw mill is down is not appropriate and is not supported by
the data
used to set the limit.
EPA should make
clear that the limit is not to be imposed on a specific mode of
operation, but
rather on the 30 day period.
60.2265
exempts cement kilns that feed non-hazardous
secondary “ingredients exclusively into the cold end of the
kiln.” In
addition, EPA has sent a letter to the
docket dated April 25, 2011 that further explains its understanding
regarding
the use these materials in both long kilns and preheater kiln systems. The
letter and the language in the proposed
regulation do not adequately clarify the exemption.
There
are many factors that determine the appropriate place
for introducing materials into the kiln system.
This is especially true for
those materials that have already been
calcined.
These factors include particle
size, emissions profile, calcination characteristics, required
conveying
equipment, impact on material flows, impact on gas flows, impact on
temperature
profile, etc.
To optimize its operation
and minimize emissions (especially CO2),
a facility may introduce a
raw material ingredient at a variety of locations along the preheater /
precalciner system or into the kiln itself.
In order to avoid confusion among
the
industry, permit writers, states and enforcement personnel, EPA
should
clearly state that kilns using non-hazardous secondary materials in the
process
as ingredients are exempt, regardless of the feed location.
[1]
Rigo, H. G. and A. J. Chandler. 1999. “Quantitation Limits
for Reference
Methods 23, 26, and 29,” J. Air &
Waste Manage. Assoc. 49:399-410.