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CDOIF

Chemical and Downstream Oil

Industries Forum

CDOIF is a collaborative venture formed to agree strategic areas for

joint industry / trade union / regulator action aimed at delivering

health, safety and environmental improvements with cross-sector

benefits.

6.2

Part 2 calculating the establishment risk frequencies

Part 1 of the risk assessment process has identified the ALARP band. Part 2 sets out

how to assess the risk from the establishment to the receptor:

x

Determine the risk from the establishment to a receptor

o

Determine the frequency of occurrence of all scenarios based on

available failure rate and/or event data (which may include

preventative or mitigatory layers and if so these should be clearly

identified in the assessments).

o

Total the frequency of all scenarios from the establishment that result

in each Consequence level (A-D) to the receptor.

o

The total frequency of events which meet or exceed each

consequence level of harm should then be compared with the

tolerability thresholds established in Part 1 (section 6.1). When

comparing the establishment frequency of lower consequence levels

(e.g. B) with the assigned ALARP bands, note that the total frequency

to be considered is the total of that and higher consequence levels

(i.e. B + C + D). An example of how aggregation is completed can be

found in section 6.2.1.

x

If the risk is still not Tolerable if ALARP (TifALARP) then assess other potential

control measures, accept/dismiss these within an ALARP demonstration and

integrate into site improvement plan as appropriate

6.2.1

Aggregating risk - Examples

Completing the initial screening (as described in section 6.1) will have discounted

potential receptors from the risk assessment process as the screening will have

determined that a MATTE is not credible.

For those substances and scenarios which do have MATTE potential, their risks to the

relevant receptor must now be determined. As it is the total risk to the receptor that is

required, i.e. from all substances, and credible scenarios, these risks must be

aggregated. Examples of how this can be achieved for each receptor are provided in the

following sections.

o

6.2.1.1 – Single substance stored in a single tank

o

6.2.1.2 – Tank farm or group of tanks containing similar substances

o

6.2.1.3 – Groups (e.g. tank farms) with dissimilar substances/incident

consequences

Guideline – Environmental Risk Tolerability for COMAH Establishments v1.0

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