GP 30-80
GP 30-80
Foreword
This is the first issue of Engineering Technical Practice (ETP) GP 30-80. This Guidance on Practice
(GP) is based on part of the heritage documents as follows:
IMSL
RP 30-5 Instrumentation and Control – Selection and Use of Equipment for
Instrument Protection Systems.
The portions of the heritage document RP 30-5 that relate to competency, management, verification,
and functional safety assessment have been replaced by GP 30-75 (Safety Instrumented Systems –
Management of the Safety Lifecycle). The remaining material from the heritage document RP 30-5 is
in this GP.
This GP reflects experience gained in implementing safety instrumented systems (SIS) since the
publication of RP 30-5. Significant differences exist between RP 30-5 and this GP, which is based on
IEC 61511 (Safety Instrumented Systems for the Process Sector).
Copyright 2007 INEOS Group. All rights reserved. The information contained in this
document is subject to the terms and conditions of the agreement or contract under which
the document was supplied to the recipient’s organization. None of the information
contained in this document shall be disclosed outside the recipient’s own organization
without the prior written permission of Site Engineering Authority, IMSL , INEOS
Group, unless the terms of such agreement or contract expressly allow.
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Table of Contents
Page
Foreword............................................................................................................................................2
Introduction.........................................................................................................................................6
1. Scope........................................................................................................................................7
2. Normative references................................................................................................................7
3. Terms and definitions................................................................................................................8
4. Symbols and abbreviations.......................................................................................................8
5. General.....................................................................................................................................9
6. Safety lifecycle – Implementation of Process Requirements Specification.............................12
7. Procedures..............................................................................................................................14
8. Selection of equipment for subsystems..................................................................................14
9. Selection of SIS architecture...................................................................................................16
10. Reliability analysis of the proposed system............................................................................17
11. Development of SIS Full Requirements Specification............................................................18
12. Design of SIS subsystems......................................................................................................19
12.1. General........................................................................................................................19
12.2. Maintenance facilities...................................................................................................20
12.3. Operations facilities......................................................................................................21
12.4. Sensors........................................................................................................................22
12.5. Logic systems..............................................................................................................23
12.6. Actuation......................................................................................................................27
12.7. Power supplies and cabling between subsystems......................................................29
13. SIS Plans................................................................................................................................29
13.1. Development of the installation plan............................................................................29
13.2. Development of the validation plan..............................................................................29
13.3. Development of the commissioning plan.....................................................................30
13.4. Development of operations and maintenance plans....................................................30
14. Installation...............................................................................................................................30
15. Validation................................................................................................................................30
16. Commissioning........................................................................................................................30
17. Verification..............................................................................................................................30
18. SIS documentation..................................................................................................................31
18.1. General........................................................................................................................31
18.2. Design dossier for safety and environmental integrity.................................................31
18.3. Design dossier for commercial integrity.......................................................................31
19. Independent functional safety assessment.............................................................................32
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List of Tables
List of Figures
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Introduction
Safety instrumented systems (SIS) have been used for many years within the process sector. The
original approach was prescriptive with standards (for example, API RP 14C in the offshore sector)
stating the specific equipment to use for a particular process application. In recent years, the increased
complexity of new applications and the complexity of new equipment becoming available for use have
made the prescriptive approach insufficient. This is particularly the case where programmable
equipment with complex failure modes is used for safety applications. Some years ago, the
international community recognised the need for new standards, and the International Electrotechnical
Commission (IEC) developed a new generic standard that adopted a risk-based approach.
The risk-based approach tailors equipment to the needs of the application and has significant safety
and economic benefits. This approach does, however, demand more management, competency,
planning, and technical judgement during all stages of realisation, from initial hazard and risk analysis
through to operation, maintenance, and modification.
The objective of this GP is to provide requirements and guidance on how to specify and implement an
SIS starting from the Process Requirements Specification through installation, validation, and
commissioning of the system. This GP relates to GIS 30-801, which addresses the specification and
procurement of the SIS logic solver subsystem.
As with all updated IMSL and industry standards, new facilities and modifications to existing
facilities should use the latest standards. While the new standards are not normally applied
retrospectively, facilities may wish to undertake a gap analysis against the new standard and address
any deficiencies.
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1. Scope
2. Normative references
The following normative documents contain requirements that, through reference in this text,
constitute requirements of this technical practice. For dated references, subsequent amendments to, or
revisions of, any of these publications do not apply. However, parties to agreements based on this
technical practice are encouraged to investigate the possibility of applying the most recent editions of
the normative documents indicated below. For undated references, the latest edition of the normative
document referred to applies.
IMSL
GP 30-75 Guidance on Practice for Safety Instrumented Systems (SIS) –
Management of the Safety Lifecycle.
GP 30-76 Guidance on Practice for Safety Instrumented Systems (SIS) –
Development of the Process Requirements Specification.
GP 30-81 Guidance on Practice for Safety Instrumented Systems (SIS) –
Operations and Maintenance.
GIS 30-801 Guidance on Industry Standard for Safety Instrumented Systems (SIS) –
Design and Engineering of Logic Solvers.
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Terms and definitions for this GP are provided in IMSL GP 30-75 and the Normative industry
standards.
For the purpose of this GP, the following symbols and abbreviations apply:
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PT Pressure transmitter.
QA Quality assurance.
5. General
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Common Requirements
relating to all lifecycle SIS Process Requirements
activities: Specification.
Functional Safety
Management.
Competency.
Verification.
SIS – Implementation of the Other Technology
Independent Functional
Safety Assessment. Process Requirements and External Risk
Specification GP 30–80. Requirements Reduction
Specification for the Realisation.
SIS.
Modification.
Decommissioning.
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e. In the U.S. and Canada, compliance with IEC 61511 may be replaced with a requirement
to comply with the equivalent clauses in OSHA, EPA, and ISA standards. (Refer to
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GP 30-75, Annex B for more detail. This annex maps some major clauses of GP 30-75 to
OSHA 29 CFR 1910.119 and ISA 84.01 standards.) In such cases, the following
documents apply:
1. ISA 84.01.
2. 29 CFR 1910.119.
3. 40 CFR, Part 68.
a. A detailed safety lifecycle shall be defined for the activities after specification of the
process requirements up to final validation.
b. The SIS implementation lifecycle shall be as shown in Figure 2 and Table 2. A modified
lifecycle may be used if justified, but this shall be documented and mapped to the
requirements of this GP and IEC 61511-1.
c. Development of plans for installation, validation, commissioning and operations and
maintenance shall be carried out during the design phase.
d. The SIS implementation lifecycle shall be integrated into the project lifecycle as described
in GP 30-75.
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Process requirement
specification from GP 30–76
Development of the
commissioning plan
Commissioning
Development of operation
and maintenance plans
Operation and maintenance
(Refer to GP 30–81)
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Selection of To select equipment that will SIS Function requirements in List of vendors and
equipment for meet the needs of the GP. SIS Process Requirement equipment types
subsystems. Specification. approved for use
Selection of SIS To select equipment SIS Integrity and robustness Minimum
architecture. architectures that meet the requirements in SIS architectures for SIS
reliability and fault tolerance Process Requirement
requirements. Specification.
Reliability analysis of To ensure the equipment and SIS Integrity and robustness Confirmed
proposed architectures meet the PFD requirements in SIS architectures and
architecture. associated with the required Process Requirement required proof test
integrity levels. Specification intervals
Development of SIS To develop the final SIS SIS SIS Process requirements SIS Full
requirements requirements specification. specification, confirmed Requirements
specification. architectures Specification
Design and To develop the detailed SIS SIS Full Requirements 1. Detail installation
procurement of the design of the SIS.. Specification drawings.
SIS subsystems. 2. SIS Procurement
specifications.
Development of the To plan the installation of the SIS SIS full specification and Installation plans and
installation plan. SIS. installation drawings. specifications.
Development of the To plan the validation of the SIS SIS full requirements Validation plans and
validation plan. SIS. specification. FAT specification.
Development of the To plan the commissioning of SIS SIS full requirements Commissioning plans.
commissioning plan. the SIS. specification.
Development of the To plan the operations and SIS SIS full requirements Operation and
operation and maintenance. specification. maintenance plan.
maintenance plan.
Installation of the SIS To install the SIS SIS SIS installation plan SIS installed
Validation of the SIS. To validate the SIS. SIS SIS validation plan. SIS validated.
Commissioning of To commission the SIS. SIS SIS commissioning plan. SIS commissioned.
the SIS.
7. Procedures
a. The following procedures shall be applied during the safety lifecycle phases of this GP:
1. General procedures specified in GP 30-75, Clause 11.1.
2. Configuration management procedures in accordance with IEC 61511-1,
Clause 5.2.7.1.1.
b. Procedures shall be applied rigorously.
c. Independent functional safety assessment shall be performed as specified in this GP,
Clause 19.
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b. General purpose industrial PLCs should not be used for implementation of SIL or EIL
rated functions.
c. Guidance provided in Annex A shall be considered in the selection of appropriate
technology for logic subsystems.
d. Preference should be given to equipment that has been assessed by an independent
organisation and shown to comply with IEC 61508-2 and IEC 61508-3 for the specified IL.
Independent organisations performing assessments should be approved by a national
accreditation body.
e. Logic systems for IL 4 applications shall be nonprogrammable.
f. Logic systems for IL 3 applications should be nonprogrammable. Proposed use of
programmable logic systems for IL 3 shall be specifically justified.
g. The type of logic system selected shall reflect the needs of the application. In selecting the
type of logic system, the following factors shall be considered:
1. Skills and experience available within the project and the application site.
2. Number of inputs and outputs, with further consideration of the following:
a) Relay systems may be cost-effective for small systems with very limited
numbers of inputs and outputs, but are not suitable for large applications.
b) Relay systems are difficult to document, test, and change.
3. Guidance included in Annex A, with respect to the choice of system.
4. Complexity of the function to be implemented, with further consideration of the
following:
a) Limited variability programmable systems may be needed for complex or
sequence applications.
b) In the case of sequence applications, the system selected should have suitable
application languages.
5. IL required, with further consideration of the following:
a) Higher ILs require a high level of assurance that the system can always fulfil the
required function under all conditions of input and output, and internal states of
the system.
b) This high level of assurance is difficult to provide with programmable systems
because testing all combinations is not practicable.
h. SIS logic solver shall be specified in accordance with GIS 30-801 and clause 12.5 of this
GP 30-80.
i. Functions that have been designated as “No special safety requirements” may be
implemented in general purpose control equipment such as DCS or PLC providing the
following conditions apply:
1. Failure of the general purpose equipment does not lead to a demand on the function
designated as “No special safety requirement”.
2. Facilities or procedures are provided to ensure overrides are not applied other than for
short periods of time.
3. Facilities or procedures are provided to ensure that settings are not modified without
approval.
4. The general purpose equipment is sufficiently reliable to justify a claimed risk
reduction factor of 10.
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a. System designers shall review the SIS Process Requirements Specification to ensure the
following:
1. Requirements are clear and unambiguous.
2. Requirements include what the system should and should not do in specified
circumstances.
3. Information is sufficient for design, specification, and final validation.
b. Arrangements of measurements, logic, and final actuation subsystems shall achieve the
functional requirements specified in the SIS Process Requirement Specification.
c. Minimum subsystem architectures should comply with fault tolerance requirements
specified in IEC 61511-1, Clause 11.4.
d. The minimum architecture to comply with IEC 61511-1, Clause 11.4 should be the starting
point in the design of the SIS system and shall then be subject to the further requirements
below.
e. Architecture selected in accordance with Subclause above should be reviewed to establish
its suitability in the event of a diagnosed failure.
f. In the event of a diagnosed dangerous failure in a subsystem, IEC 61511-1, Clause 11.3
shall apply.
g. If the mode of operation is continuous/high demand and a nonredundant architecture is
applied, the process shall be put into a safe state upon detection of a dangerous failure.
This condition may be implemented automatically or by an operator action.
h. If the mode of operation is low demand and a nonredundant architecture is applied, the
process shall be put into a safe state, or additional measures and constraints applied
equivalent to the safety provided by SIS.
i. In accordance with IEC 61511-1, Clause 11.3, in most cases of nonredundant systems, the
process shall be shut down upon a diagnosed failure. This shutdown may not be acceptable
from a production viewpoint, in which case the fault tolerance of the system should be
increased.
j. Measurement and logic subsystems shall be failure robust if annualised cost of additional
capital and maintenance of additional hardware needed is less than calculated annual cost
of spurious trips.
k. Architectures used for programmable logic systems and digital communications between
SIS logic solver and DCS shall be failure robust.
l. Failure robust architecture for final elements should be used only if practicable and if it can
be shown that the increase in dangerous failure rate is small.
a. Maximum interval between proof testing for SIS subsystems shall be determined,
considering the following:
1. Interval at which the process plant will shut down for inspection or maintenance.
2. Availability of spare process equipment that would allow testing of SIS subsystems
without disruption to production.
3. Degradation mechanisms that could result in failure to function (for example, wear,
cavitation, and blockage).
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a. SIS Full Requirements Specification shall be prepared in accordance with IEC 61511-1,
Clause 10.3.
b. SIS Full Requirements Specification shall be verified against the Process Requirements
Specification.
c. SIS Full Requirements Specification shall encompass or reference all parts of the system
that function to terminate the identified hazards. For example:
1. Measurement devices.
2. Logic systems.
3. Final actuation devices.
4. Power supplies, if failure would lead to failure to function.
5. Additional elements (for example, interfaces and barriers).
d. Necessary functions may be executed by a single system or may be allocated to a number
of systems, depending on:
1. Functionality needed.
2. Size of the system.
3. Required IL.
e. Subsystem specifications shall be prepared for components of the system that will be
purchased as separate parts.
f. The subsystem specification shall reference the overall SIS Full Requirements
Specification and include functional requirements and details of IL requirements.
g. Subsystem specifications shall include response requirements derived from the SIS Process
Requirements Specification.
h. Subsystems with specified ILs of 3 or higher shall be redundant.
i. For systems applied offshore, account should be taken of the minimum redundancy
requirements of ISO 10418.
j. Component parts of subsystems shall be arranged such that loss of signal or power will not
cause an unsafe failure.
k. Equipment vendors shall be required to supply information on product history of failure
and degradation.
l. Equipment vendors shall be required to agree to supply information in the future about
reported failures and degradation.
12.1. General
a. SIS shall be designed in accordance with IEC 61511-1, Clause 11.
b. Application software shall be designed in accordance with IEC 61511-1, Clause 12.
c. To warn the operator, trip functions should be preceded by a pre-alarm from a separate
device serving the same process variable or condition.
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d. During design, consideration should be given to the need for security as follows:
1. Equipment should be installed and located to maintain the required integrity by
preventing unauthorised or inadvertent modification of SIS functions.
2. To maintain SIS integrity, consideration should be given to sensor and valve security
as well as the security of the SIS logic solver, application software, and user interface.
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k. For IL 1 applications, online testing of final actuator devices may not be required. An
adequate level of integrity may be achieved by testing during plant or spared equipment
shutdown.
12.4. Sensors
a. Sensors shall comply with IEC 61511-1, Clause 11.6.
b. Inputs to the SIS should be through continuous analogue measurement devices, rather than
switches. These inputs should not use shared media (for example, Fieldbus) at IL 1 or
higher.
c. Transmitters used for trip shall:
1. Be separate from transmitters used for measurement, control, and alarm purposes
(subject to the exception in Clause below).
2. Use separate process tappings, particularly where impulse lines could become
blocked (plugged).
d. Trip and measurement transmitter sensors shall be in the same range, so that signal
comparison can be performed in the DCS [process automation system (PAS)] with alarm
on deviation above a set margin, typically 3%–5%. In addition:
1. Implementation shall be such that the integrity of the trip transmitter loop cannot be
impaired by failures of the DCS (PAS) or the communication system.
2. Credit for improved diagnostic coverage or safe failure fraction can then be taken [up
to the maximum 90% limit, if diagnostics are installed in the DCS (PAS)].
e. Multiple transmitters for the same measurement may be used for trip (in a voting
configuration) and measurement, control, and alarm purposes if:
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1. Credible faults in the measurement, control, and alarm functionality cannot cause loss
of the safety function.
2. IL is 2 or lower.
f. Measurement devices used to initiate SIS action when the parameter exceeds a specified
level shall be reverse ranged or an individual alarm shall indicate loss of signal.
g. Measurements used as inputs to the SIS should relate closely to the potential hazard.
Inferred measurements should be avoided.
h. In selecting the value at which a shutdown is initiated, account shall be taken of the
following:
1. Need for a margin above the normal operating range to ensure transients or errors in
measurement do not lead to spurious tripping.
2. Need for a margin before reaching a limit point (for example, vessel design pressure,
setpoint of a relief valve, or overflow level). High pressure trip settings should not
exceed 90% of the setpoint of the associated relief valve.
3. Process dynamics in the event of a demand.
i. Sensors shall have ranges selected for effective accuracy at the shutdown value of the
abnormal plant condition. Additional over-range protection (for example, low pressure
switches or transmitters) may be required. The switching differential should be checked to
ensure that the switch or trip amplifier resets when plant conditions return to normal.
j. If over- or under-range protection is provided, consideration should be given to the effect
on reliability.
k. In selecting sensors to use for a response specified in the SIS Process Requirements
Specification, account shall be taken of the process delay at the point of measurement.
l. The following shall not be used on protective systems:
1. Mercury bottles as switching mechanism.
2. Filled systems for temperature switching.
3. Instruments that use self-balancing potentiometers.
4. Differential pressure switches where the switching differential is less than 10% of
absolute pressure.
12.5.1. General
Organisations responsible for design and supply of SIS logic solvers shall be supplied with the
following information in the requisition:
a. Scope of supply as detailed in clause below.
b. Copy of GIS 30-801, without blue comments text, detailing general requirements for logic
solvers.
c. Dependent on the nature of the contract between IMSL or its engineering contractor and
the supplier of the SIS logic solver(s) there may be opportunity for an iterative process to
finalise the requirements specification to maximise ability of the supplier to offer their
standard specification while still meeting IMSL requirements to achieve the most cost-
effective, compliant solution.
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12.5.2.1. General
a. Scope of supply shall include equipment, services, and information required for provision,
installation, testing, and maintenance of the SIS logic solver.
b. Scope of supply may include provision of information to enable the proposed logic solver
to be compliance-assessed.
12.5.2.3. Configuration
Scope of supply may include the following configuration activities:
a. Configuration of I/O in accordance with I/O listings in the requisition. This includes
diagnostic functions to support selected I/O field devices. It may also include any “second
fault timers” required to manage allowable first fault periods in voted field devices where
the allowable time to repair is exceeded.
b. Configuration of SIS logic solver communications in accordance with communication
listings in the requisition.
c. Configuration of the SIS to perform functions detailed in the documents listed in the
requisition and provided on a medium as indicated in the requisition.
d. Configuration of trip settings, timers, etc.
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2. A written description.
3. A functional logic diagram drawn in failsafe mode using Boolean logic gates “and”,
“or” etc.
12.6. Actuation
a. Devices used for final actuation shall comply with IEC 61511-1, Clause 11.6.
b. Operational constraints may make proof testing of the final actuated valve unfeasible at the
frequency necessary to ensure the target reliability is achieved. In such cases, the following
alternatives should be considered:
1. Facilities to allow partial stroke testing of the valve.
2. Additional valves arranged in parallel, with separate isolation and depressuring
facilities for online testing and maintenance without interruption of the process.
c. Speed and sequencing of operation of the valves shall be such that action does not cause
pressure surges in the pipework that may lead to equipment damage.
d. Trip valves used as part of a safety function shall not be used for other functions, unless it
can be shown that valve failures will not lead to a demand on the system. In addition:
1. Such valves shall have no manual bypass.
2. Handwheels shall not be installed.
3. If dual parallel valves are installed to enable online testing, isolation valves shall be
secured in such a way as to prevent unauthorised operation.
e. Single control valves may be used as the sole method of asset protection under the
following conditions:
1. Failure to function results only in commercial consequences.
2. Integrity level requirements are limited to IL 1.
3. Dangerous failure rate of the valve can be shown to be two orders of magnitude less
than the expected demand rate.
f. Shutdown and blowdown valves shall be selected in accordance with IMSL GP 62 series
practices.
g. Relays and solenoids shall be installed with correctly rated suppression devices connected
directly to the coils.
h. Solenoid coils shall:
1. Be dc operated.
2. Have insulation rated for continuous operation at the maximum ambient temperature,
with Class A of IEC 60085 as an overall minimum requirement.
3. Be capable of dissipating additional power resulting from a higher than normal supply
voltage during online boost charging of battery systems.
i. Solenoid valves should latch in the shutdown position and have facilities for local manual
reset only except as otherwise permitted in clause below.
j. If agreed with local management, solenoids may be reset from a central location or in the
field on a group basis (except for applications on fuel lines).
k. Actuation of electrical equipment by protective circuits shall be through interposing relays
located in separate cabinets.
l. Use of electrically driven valves are nonpreferred because of difficulty in ensuring a
backup power supply.
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m. Electric motor operated valve actuators for valves on protective duty shall conform to
GP 12-70. In addition:
1. If Local/Off/Remote switches are provided, they shall be capable of being padlocked.
2. An alarm should be annunciated in the control room to indicate that the motor
operated valve is inoperative for any reason (for example, power failure, or Stop
button pressed).
3. The reversing starter, interlocking, and signalling switches shall be integral with the
actuator.
n. If two or more electrically operated valves are to be interlocked (for example, to ensure
that a bypass valve is open before the line main valve is permitted to close and vice versa),
operation shall be interlocked only in the main electrical contactor circuits. Design shall
ensure that:
1. Interlocks are effective in all remote and automatic modes of control. If interlocking
is implemented in the main contactor, it should be interlocked in both local and
remote modes.
2. There are physical means of preventing selection of the local control mode.
3. Local mode selection should be prevented by padlocking the selector switch in the
auto or remote position. The selector switch should be unlocked only under a
controlled procedure.
o. Actuators installed to emergency shutdown valves on applications with safety,
environmental, or commercial consequences and with IL 3 or greater shall:
1. Comply with GP 62 series practices.
2. Have transducers to measure online performance.
3. Have valve fault alarms for operators when the actuator does not reach the required
position within a predetermined time period after action is initiated.
4. Have fault alarm power supply that is independent of the actuator power supply.
p. If valve status indication is required, proximity switches should be used.
q. If high diagnostic coverage is required, position transmitters on valves may be preferred
over position switches because they provide an indication over the full range of valve
travel.
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14. Installation
15. Validation
16. Commissioning
17. Verification
18.1. General
a. Documentation shall comply with IEC 61511-1, Clause 19.
b. Comprehensive design dossiers describing all aspects of the SIS shall be developed for
distribution to operations and maintenance management.
c. Design dossiers shall be in both paper and electronic format.
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g. Details of the Quality Assurance procedures that have been applied to the system design
and during system manufacture.
h. Details of the factory acceptance tests considered necessary at the Vendor location and the
onsite site acceptance tests.
i. A record of the factory acceptance tests carried out at the Vendor location and the onsite
site acceptance tests before and during commissioning.
j. Details of proof tests necessary to ensure integrity is maintained in operation, including
details of test procedure and test programme.
k. Details of operational requirements and assumptions on how the system is to be operated,
which are included in the reliability analysis.
l. A list of all safety-critical items. These should not be modified without reviewing the
safety implications.
m. Design specifications for all safety-critical items.
n. The results of independent functional safety assessments.
o. Detailed design drawings showing process, electrical, pneumatic, hydraulic, and power
supply arrangements.
a. The design of the SIS shall be subject to independent functional safety assessment in
accordance with GP 30-75, Clause 11.2.
b. Independent functional capability assessment shall be performed at two stages during the
activities covered in this GP:
1. After development of the SIS specification to confirm that all actions from previous
independent functional safety assessments have been implemented and that the design
of the SIS meets requirements.
2. Before commissioning to confirm that the SIS is correctly installed and appropriate
plans prepared for commissioning and operation and maintenance are in place.
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Annex A
(Informative)
Choice of equipment or logic subsystems
A.1. General
The choice of equipment for logic subsystems is complex. The decision impacts cost and
schedule during project implementation and has a significant effect during the operations and
maintenance phase discussed in GP 30-81.
This annex gives information that should be considered when selecting such equipment.
A.2.1.1. General
a. Relay systems should be used if the ease of application, reliability of operation, and low
cost are important. Typical applications include:
1. Interlocking and protection of spare pumps.
2. Protection of self-contained packages that need not be integrated with the remainder
of the process protection.
b. Relay systems can be cumbersome to design as fault-tolerant systems and have very
limited diagnostics capability.
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A.2.3.1. General
Programmable systems may be considered in the following three categories:
a. Fixed program system – the function of the system is fixed and unchangeable.
b. Limited variability system – the user can configure the particular logic requirement,
typically provided by a PLC.
c. Full variability system – the system provides:
1. Facilities similar to those offered by limited variability systems.
2. Facilities similar to those in a minicomputer based real-time system (for example,
displays, high-level languages, and data links).
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d. Ease of reconfiguration.
e. Fault diagnosis.
f. Simple interface to computers.
g. Can be self-documenting.
a. It can be difficult to demonstrate that equipment for logic processing can achieve a
specified IL.
b. Assessment of equipment for compliance requires special skills and may take significant
time.
c. The following evidence is valuable when determining the suitability of equipment for
specified ILs:
1. Equipment has been shown by independent compliance assessment to comply with
IEC 61508.
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2. Systems have been independently assessed to previous standards (for example, the
German standard DIN VDE0801) for the associated risk class.
d. Independent compliance assessments on equipment are performed by TUV Rheinland in
Germany, FM Global Research in the U.S., INERIS in France, and others.
e. SIRA Test and Certification in the U.K. perform assessments under the CASS Scheme on
the capability of organisations to manage functional safety.
f. Reasons why general-purpose programmable electronic systems (for example, industrial
PLCs, which are not specifically developed and assessed for safety applications) should
not be used for logic processing include:
1. Failure and failure modes – Because a single microprocessor is often used to execute
the logic of the application, the failure of the microprocessor or associated
components usually result in some or all logic being halted thus plant protection may
be lost.
2. Predicting the mechanism of a hardware failure is unlikely and a fault may lie
unrevealed. Therefore:
a) To overcome these two difficulties, it is necessary to arrange (usually by
external equipment) to detect failure and take action (usually by forcing plant
outputs to a safe state).
b) To reveal dormant faults, regular testing of the system is necessary.
c) Considering the outcome of the failure states is of utmost importance in facility
design.
3. In addition to hardware faults, software problems may occur. Although software
failure can not occur, software faults may result from either:
a) Operating system software being insufficiently tested to reveal faults.
b) Application software being unable to cope with a certain facility condition.
4. Modifications – Programmable electronic systems provide flexibility and
convenience in configuring logic to meet facility requirements. A danger exists that if
such flexibility is applied in an uncontrolled manner, plant protection may be
downgraded due to indiscriminate modification of application software. Therefore,
application software should have closely controlled access and modification
procedures.
5. Overrides and interlocks – If application software has override (bypasses) or interlock
(permissive logic) capabilities, operators and plant managers should be informed that
the plant is being operated in such a manner. If the application of overrides (bypasses)
is not closely monitored, a danger exists that plant protection may be gradually
downgraded.
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Annex B
(Informative)
Typical subsystem architectures
B.1. Introduction
a. This annex includes hardware options that normally meet the PFD and fault tolerance
requirements for a specified IL for a standard proof test interval of 1 year.
b. This annex is to be used for initial SIS design. Once the basic hardware selection has been
completed and data becomes available on the equipment to be used, a formal study will be
needed to confirm that requirements of IEC 61511-1 have been satisfied.
B.2. Architectures
a. Architecture required for a specified IL depends on a number of factors, not all of which
are known at an early stage.
b. During project execution, agreement upon an initial architecture to allow design and
procurement activities to proceed is often an early requirement.
c. Factors to consider in determining an architecture are listed below, along with assumptions
made in these example configurations:
1. Failure rate of subsystem components – a transmitter has been assumed and OREDA
has been used as the data source.
2. Diagnostic coverage of subsystem components – assumed to be zero.
3. Safe failure fraction of subsystem components – assumed to be higher than 60%
based on assumption that signals will go to the dangerous state upon loss of power or
signal.
4. Number of actions that need to function to achieve success – assumed that one input
is required to initiate the logic and one output is required to isolate one stream only.
5. Redundancy arrangement of subsystems – as indicated.
6. Beta factor – assumed to be 5%.
7. Proof test interval of components – assumed to be 1 year.
8. Test coverage of proof testing – assumed to be 100%.
B.3. IL 1 configuration
a. Architecture shown in Figure B.1 should provide appropriate reliability and fault tolerance
on the following conditions:
1. Control valve failure does not cause a demand on the SIS.
2. Tight shutoff is not required.
3. Control valve is not subject to such erosion or corrosion that it would not be able to
achieve shutoff requirements.
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b. Architecture shown in Figure B.2 should provide appropriate reliability and fault tolerance
for IL 1 applications that do not meet the application conditions for Figure B.1.
B.4. IL 2 configuration
a. Architecture shown in Figure B.3 should provide appropriate reliability and fault tolerance
on the following conditions:
1. Control valve failure does not cause a demand on the SIS.
2. Tight shutoff is not required.
3. Control valve is not subject to such erosion or corrosion that it would not be able to
achieve the shutoff requirements.
b. Where the above conditions are not satisfied, the control valve shall be replaced with a
shutoff valve.
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B.5. IL 3 configuration
a. Architecture shown in Figure B.4 should provide appropriate reliability and fault tolerance
on the following conditions:
1. Control valve failure does not cause a demand on the SIS.
2. Tight shutoff is not required.
3. Control valve is not subject to such erosion or corrosion that it would not be able to
achieve the shutoff requirements.
b. To reduce common cause, consideration should be given to multiple physical
measurements (for example, pressure and temperature). Options available include use of:
1. Single solenoid-operated valve (SOV).
2. Shorter test interval.
c. Architecture shown in Figure B.5 should provide appropriate reliability and fault tolerance
for IL 3 applications that do not meet the application conditions for Figure B.4.
d. If application conditions for B.4 are not met, limited credit should be taken for the control
valve because, for some demands, the control valve is incapable of terminating the hazard.
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e. IL 3 integrity should also be achieved with the two shutoff valves and without the control
valve.
B.6. IL 4 configuration
a. A formal quantitative risk and reliability assessment is required in all cases for IL 4.
b. Reliability assessments should include:
1. Detailed consideration of common cause factors.
2. Human factor issues in maintenance, testing, and operation.
c. To achieve IL 4, consideration should be given to using multiple diverse physical
measurement and multiple diverse effects (for example, stop pump as well as close valves).
d. IL 4 will likely require shorter test intervals than 1 year.
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Annex C
(Informative)
System design for robustness
C.1. Introduction
a. Spurious tripping of an SIS due to revealed (safe) faults may result in the following
consequences:
1. Lost production and/or lost market opportunities.
2. Lost inventory.
3. Environmental impact due to flaring or venting.
4. Additional hazards during shutdown or subsequent startup due to failures in the
process equipment or the SIS.
5. Stressing of equipment due to sudden change in system (for example, pressure,
temperature) that may, in some cases, cause the need for earlier maintenance.
6. Additional demands on other protection functions.
b. The first two consequences in the above list may be determined on a quantitative basis.
Remaining items should be considered on a qualitative basis.
c. The minimum SIS subsystem architecture required to achieve a specified IL should be
reviewed to determine whether additional equipment is justified to reduce probability of
the consequences listed above.
d. This annex describes a procedure to evaluate whether expenditure on additional equipment
is justified.
a. Basic consequences of spurious tripping should have been evaluated when the SIS Process
Requirements Specification was developed as described in GP 30-76.
b. To evaluate expected annual costs of these consequences, information is required on
reliability of individual elements of the system.
c. In most cases, vendors should be able to provide data on equipment reliability. Such data
may also be available from within IMSL or from industry databases. However, care is
needed to ensure that provided data relates to spurious trip rate of the specific function
rather than overall reliability of the component.
d. In the case of an output card within an SIS logic solver, vendors may provide an overall
figure for the rate of failure to a safe condition. This figure may be relatively high because
it may include all output channels and ancillary functions (for example, communication
interfaces for status reporting). Data used should relate only to failures that cause change
of state for specific outputs used by the safety function. Care is also needed in cases where
diagnostics can be programmed to force signals to the high or low state.
e. Requirements that relate to actions on diagnosis of a fault in Clause 9.1.e through i of this
GP and IEC 61511-1, Clause 11.3 should be noted. Normally, a shutdown should be
assumed if a fault is diagnosed in a nonredundant system.
f. Evaluation of cost of spurious trips per year (CST) should be investigated under the
following three headings:
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1. Costs associated with the sensor and logic function. In general, architecture for logic
inputs, processing, and outputs follow the same architecture as the sensor
arrangement.
2. Costs associated with solenoid valve failures. In some cases, it is practicable to reduce
spurious trip rate by using robust architectures for solenoid valves.
3. Costs associated with the valve and actuator function. In general, costs of achieving
robust architectures for process valves are higher than costs associated with spurious
trips. Arranging valves on a 2oo2 basis also leads to an increase in average PFD.
a. For each function that includes a nonrobust subsystem, the costs of additional equipment
(CAE) for robustness should be evaluated.
b. Additional costs should be evaluated under the same three headings as listed in Clause C.2
above. Additional equipment required and additional costs are vendor specific. In general,
1oo2D architectures are more cost-effective than 2oo3 architectures.
c. Cost criteria for robustness depends on project requirements for rate of return. In general,
the required payback period is a maximum of 3 years, but alternate criteria may be
preferred on a specific project. In performing calculations, it is normal to assume that the
CST is reduced to negligible levels once a robust architecture is used.
d. Costs should be annualised by:
1. Taking additional capital costs associated with purchase, design, and installation.
2. Dividing by 3.
3. Adding annual maintenance costs for testing and equipment replacement.
C.5. Example
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Annex D
(Informative)
Example of the development of an architecture for a SIS
D.1. General
This annex describes an example architecture that could be developed for SIS.
a. The process considered in this example involves the reaction of two liquids within a
catalytic reactor.
b. The reactor is designed for the process pressure and temperature that exists under normal
operation, but not for the pressure if heat is not removed or the exit valves are closed.
c. The two liquids are supplied from headers at a pressure above reactor design pressure.
d. The reactor has a thermal relief valve.
e. The pressure in the headers is sufficient to cause a major failure of the reactor if the outlet
flow is stopped. The pressure will also rise above failure pressure of the reactor if
insufficient cooling is provided.
f. The reactor is provided with an SIS to prevent overpressure.
g. The arrangement of process and SIS is shown in Figure D.1.
PV
Logic
PT
FIC
Reactor
TT TCV Cooling
water
Chemical A
FIC LT
FCV ESDV
FT
Chemical B
LIC LCV
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The following process requirements for this example are derived from Annex E of GP 30-76:
a. Process function – If the pressure in reaction vessel XYZ rises above 90% of the maximum
allowable working pressure, the flow of Chemical A and Chemical B shall be reduced
below 25% of the capacity of the thermal relief valve within 5 seconds.
b. Integrity level – The function has the following integrity levels – SIL 2, EIL 0, and CIL 2.
c. Mode of operation – Demand mode.
d. Spurious tripping will result in a commercial loss of $10 000.
a. In this example, the minimum architecture for each subsystem is determined as follows:
1. Sensor – The sensors have been compliance assessed as meeting SIL 2 requirements
for a nonredundant configuration. In addition:
a) Clause 9.1.e through i of this GP requires a review to consider suitability in the
event of a failure being diagnosed.
b) The sensors have comprehensive diagnostics.
c) The system is operating in low-demand mode.
d) In the event of a dangerous failure being detected, there is no equivalent
protection available from other safety layers.
e) The requirements of IEC 61511-1, Clause 11.3 are to shut down in the event of a
failure being diagnosed.
f) The failure rate of the sensors is low and it is considered that this is acceptable.
g) Clause 9.1.j of this GP requires consideration of failure robustness.
h) The CST has been determined to be $10 000.
i) From Table D.1, it has been determined that failure robustness is not justified in
this case.
2. Logic system – The SIS logic solver has been compliance assessed as meeting SIL 2
requirements for a nonredundant configuration. In addition:
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a. Tables in IEC 61508-6 are used to determine the average PFD for the minimum
architectures as developed in this example.
b. Subsystem vendors have provided information on the dangerous failure rate of the
equipment they provide.
c. The SIS is operating in demand mode, so the appropriate measure is average PFD.
d. A minimum proof test interval of 6 months has been agreed upon with the facility
maintenance team.
e. The contribution of each subsystem is shown in Table D.2.
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f. Results of the reliability calculation are also shown in Table D.2. Further explanation of
the calculation method is included in IEC 61508-6.
g. The average PFD for the overall system is calculated as 8,9E–3. This is within the SIL 2
range, so the proposed architecture is acceptable from a reliability consideration.
h. Further optimisation of test intervals may be considered. Analysis of the figures suggests
that the test interval for sensors and logic may be extended without significant impact on
the overall reliability.
The selected architecture for the example application is shown in Figure D.2.
Logic architecture
ESDV
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Bibliography
[1] 29 CFR 1910.119 - Process Safety Management of Highly Hazardous Chemicals, Explosives and
Blasting Agents.
[2] 40 CFR Part 68 - Risk Management Programs for Chemical Accidental Release Prevention.
[3] ISO 9000 Family – ISO 9000 Compendium – International Standards for Quality Management.
[4] ESR.97.ER.081 – On-line Testing of Emergency Shutdown Valves, issued in November 1997. A
IMSL internal publication available from Exploration and Production Technology Group, Sunbury,
UK.
[11] DIN VDE0801 - Principles for Computers in Safety-Related Systems (German National Standard).
[12] IEC 61000-1-2 - Electromagnetic Compatibility (EMC) – Part 1-2: General – Methodology for the
achievement of functional safety of electrical and electronic equipment with regard to electromagnetic
phenomena.
[13] PIP PCESS001 – Safety Instrumented Systems Guidelines, issued December 1999.
[14] UKOOA Guidelines for Instrument-Based Protective Systems, Issue No. 2, November 1999.
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