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SAFETY in OVERPRESSURE RELIEVING SYSTEMS - KLM ...

SAFETY in OVERPRESSURE RELIEVING SYSTEMS - KLM ...

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<strong>KLM</strong> TechnologyGroupPractical Eng<strong>in</strong>eer<strong>in</strong>g Guidel<strong>in</strong>esfor Process<strong>in</strong>g Plant Solutions<strong>SAFETY</strong> <strong>in</strong> <strong>OVERPRESSURE</strong><strong>RELIEVING</strong> <strong>SYSTEMS</strong>ENGINEERING DESIGN GUIDELINESPage 18 of 64Rev: 01October 20113. Validate, start-up, operate and ma<strong>in</strong>ta<strong>in</strong> the strategy - implement the SISfollow<strong>in</strong>g the design basis and detailed design documentation and def<strong>in</strong>e what isrequired of operation and ma<strong>in</strong>tenance personnel to susta<strong>in</strong> the SIL4. Manage changes to the strategy - ensure the SIS meets the target SIL bymonitor<strong>in</strong>g operation, <strong>in</strong>spection, test, and ma<strong>in</strong>tenance records and mak<strong>in</strong>gchanges as necessary to improve its performanceValidation plann<strong>in</strong>g of the SIS should def<strong>in</strong>e all activities required for validation. Thefollow<strong>in</strong>g items shall be <strong>in</strong>cluded:1. The validation activities, <strong>in</strong>clud<strong>in</strong>g validation of the SIS with respect to the safetyrequirements specification and implementation and resolution of result<strong>in</strong>grecommendations;2. Validation of all relevant modes of operation of the process and its associatedequipment <strong>in</strong>clud<strong>in</strong>g:a. Preparation for use <strong>in</strong>clud<strong>in</strong>g sett<strong>in</strong>g and adjustment;b. Start-up, teach, automatic, manual, semi-automatic and steady state ofoperation;c. Re-sett<strong>in</strong>g, shut down and ma<strong>in</strong>tenance;d. Reasonably foreseeable abnormal conditions.3. The procedures, measures and techniques to be used for validation;4. Reference to <strong>in</strong>formation aga<strong>in</strong>st which the validation shall be carried out (e.g.,cause and effect chart, system control diagrams).5. When the activities shall take place;6. The persons, departments and organizations responsible for the activities andlevels of <strong>in</strong>dependence for validation activities;SIS safety validation shall mean all necessary activities to validate that the <strong>in</strong>stalled andmechanical completed SIS and its associated <strong>in</strong>strumented functions, meets therequirements as stated <strong>in</strong> the Safety Requirement Specification (SRS). The validation ofthe safety <strong>in</strong>strumented system and its associated safety <strong>in</strong>strumented functions shall becarried out <strong>in</strong> accordance with the safety <strong>in</strong>strumented system validation plann<strong>in</strong>g.Validation activities shall as a m<strong>in</strong>imum confirm that:These design guidel<strong>in</strong>e are believed to be as accurate as possible, but are very general and not for specific design cases.They were designed for eng<strong>in</strong>eers to do prelim<strong>in</strong>ary designs and process specification sheets. The f<strong>in</strong>al design mustalways be guaranteed for the service selected by the manufactur<strong>in</strong>g vendor, but these guidel<strong>in</strong>es will greatly reduce theamount of up front eng<strong>in</strong>eer<strong>in</strong>g hours that are required to develop the f<strong>in</strong>al design. The guidel<strong>in</strong>es are a tra<strong>in</strong><strong>in</strong>g tool foryoung eng<strong>in</strong>eers or a resource for eng<strong>in</strong>eers with experience.This document is entrusted to the recipient personally, but the copyright rema<strong>in</strong>s with us. It must not be copied,reproduced or <strong>in</strong> any way communicated or made accessible to third parties without our written consent.

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