The EPA published a notice of proposed rulemaking (NPRM) in
Monday’s Federal Register (available on-line today; 81 FR
13637-13712) for revisions to their Risk Management Program (RMP)
regulations. The revisions are mostly in response to the President’s executive
order on Chemical Safety and Security (EO
13650) and the EPA’s request
for information (RFI) supporting that EO.
NPRM Overview
The major points of the NPRM address the following three
areas:
The NPRM proposed three changes to the accident prevention
program. These include:
• Requiring all
facilities with Program 2 or 3 processes to conduct a root cause analysis as
part of an incident investigation of a catastrophic release or an incident that
could have reasonably resulted in a catastrophic release (i.e., a near-miss);
• Requiring regulated
facilities with Program 2 or 3 processes to contract with an independent third-party
to perform a compliance audit after the facility has a reportable release; and
• Requiring selected
facilities to conduct a safer technology and alternatives analysis (STAA) as
part of their PHA, and to evaluate the feasibility of any inherently safer
technology (IST) identified.
The NPRM proposed four changes to the emergency response
enhancements. These include:
• Requiring all
facilities with Program 2 or 3 processes to coordinate with the local emergency
response agencies at least once a year to ensure that resources and
capabilities are in place to respond to an accidental release of a regulated
substance;
• Requiring all
facilities with Program 2 or 3 processes to conduct notification exercises
annually to ensure that their emergency contact information is accurate and
complete; and
• Requiring all
facilities subject to the emergency response program requirements of subpart E
of the rule (or “responding facilities”) conduct a full field exercise at least
once every five years and one tabletop exercise annually in the other years;
and
• Requiring responding
facilities that have an RMP reportable accident to conduct a full field
exercise within a year of the accident.
The NPRM proposed five changes to the enhanced availability
of information. These include:
• Requiring all
facilities to provide certain basic information to the public through easily
accessible means such as a facility Web site or at public libraries or
government offices;
• Requiring a subset
of facilities, upon request, to provide the Local Emergency Planning Committee
(LEPC) with summaries related to: compliance, emergency response exercises, accident
history and investigation reports, and any ISTs implemented at the facility;
• Requiring all
facilities to hold a public meeting for the local community within a specified
timeframe after an RMP reportable accident;
• Proposing revisions
to clarify or simplify the RMP submission; and
• Proposing technical
corrections to various provisions of the rule.
EPA Seeking Guidance
In addition to the proposed changes in the NPRM, the EPA is
also looking for public input on additional changes to the RMP that might be
included in future rulemaking. For the accident prevention program, the EPA is
looking for information on additional
requirements for:
• Location of stationary sources
(related to their proximity to public receptors); or
• Emergency shutdown systems
Public Comments
The EPA is soliciting public
feedback on the NPRM. Comments may be submitted via the Federal eRulemaking
Portal (www.Regulations.gov; Docket # EPA-HQ-OEM-2015-072).
Comments should be received by May 13th, 2016.
The EPA is currently planning one public hearing to
allow personnel to provide oral comments about the NPRM. The hearing will be
held on March 29th, 2016 in Washington, DC. Advanced registration
for a chance to speak at the hearing is strongly suggested. You are supposed to
be able to register on-line here,
but the site is not set up as of the time I’m writing this post (3-12-16 9:00
pm CST). I suspect that it will be set up sometime on Monday.
Commentary
While I have not had a chance to complete a detailed review
of the extensive NPRM, it seems clear even at the broad overview provided here
that no one is going to be fully satisfied with what the NPRM proposes or
ignores. In general I think that that should be the mark of any good
regulation, but we will have to wait and see if that is the specific case here.
The topic of inherently safer technology provides a good
case in point. Environmental and many safety advocates have long pushed for the
EPA to require RMP facilities to implement IST improvements to their chemical
processes. While there is not a consensus definition of what an IST improvement
would be, the more vocal advocates press for a replacement of toxic chemicals
with safer alternatives where ever possible, while more moderate advocates
would replace the ‘where ever possible’ with ‘where practical’.
Industry, on the other hand, maintains that it already has
conducted IST analysis as part of their standard engineering practices and that
the decision to implement a specific IST improvement is a risk-management decision
that is only able to be made by facility owners and engineers based upon their
unique knowledge of the process.
At first glance it looks like the EPA in this NPRM has taken
a middle road or requiring companies to formally document their IST analysis
process. Business will most likely
complain that this is bureaucratic make-work that will cost money without
providing any safety improvement. The safety and environmental activists will
certainly agree that the study provision will not provide any safety
improvement; that such improvements can only come with mandatory IST
implementation. It will take a detailed look at the IST process outlined in
this NPRM (I’ll be doing this in some later blog post) to determine which is
more nearly correct about their assessment.
As usual, readers of this blog can expect that I will be
taking more detailed looks at the actual language of the proposed changes in a
series of future blog posts. Two things that I can tell you at this point:
first, I expect that multiple parties will petition for a longer comment period
(90 days instead of 60); second, I expect that there will also be multiple
requests for regional public hearings. I really expect that both requests will
be honored.
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