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|z (OCoLC)1352034780
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|a pcc
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|a TP150.S24
|b A44 2023
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|a TP150.S24
|b F7 2023
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|a 660/.2804
|2 23/eng/20230111
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|a UAMI
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|a American Institute of Chemical Engineers.
|b Center for Chemical Process Safety,
|e author.
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1 |
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|a Guidelines for revalidating a process hazard analysis /
|c Center for Chemical Process Safety.
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250 |
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|a Second edition.
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264 |
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1 |
|a Hoboken, NJ :
|b John Wiley & Sons, Inc. :
|b American Institute of Chemical Engineers,
|c 2023.
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264 |
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|c ©2023
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|a 1 online resource (xxi, 218 pages) :
|b illustrations.
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336 |
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|a text
|b txt
|2 rdacontent
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337 |
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Center for Chemical Process Safety guidelines series
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|a Includes bibliographical references and index.
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|a Cover -- Title Page -- Copyright -- Table Of Contents -- List Of Tables -- List Of Figures -- Acronyms And Abbreviations -- Glossary And Nomenclature -- Acknowledgments -- Preface -- Dedication -- Introduction -- Objective Of This Book -- Scope Of This Book -- How To Use This Guidelines Book -- 1 Overview Of The Pha Revalidation Process -- 1.1 What Is A Pha And What Is A Pha Intended To Accomplish? -- 1.2 Overview Of Typical Pha Activities -- 1.2.1 Pha Core Methodology -- 1.2.2 Pha Complementary Analyses -- 1.3 General Risk Assessment Principles -- 1.3.1 Risk And Risk Toler -- 1.3.2 Supplemental Risk Assessments -- 1.4 Pha Revalidation Objectives -- 1.5 Pha Revalidation Concept -- 1.6 Pha Revalidation Cycle -- 1.7 The Role Of A Pha Revalidation Procedure -- 1.8 Relationship Of Rbps Pillars To A Pha Revalidation -- 2 Pha Revalidation Requirements -- 2.1 External Legal/Regulatory Requirements -- 2.1.1 General Obligations -- 2.1.2 Specific Ragageps -- 2.2 Internal Company Policy Requirements -- 2.2.1 Compliance-Driven Policies -- 2.2.2 Ehs-Driven Policies -- 2.2.3 Value-Driven Policies -- 2.3 Internal Company Drivers That Impact Revalidation -- 2.4 Principles For Successful Definition Of Revalidation Requirements -- 3 Evaluating The Prior Pha -- 3.1 Prior Pha Essential Criteria -- 3.1.1 Prior Pha Methodology Used -- 3.1.2 Prior Pha Inputs -- 3.1.3 Prior Pha Scope -- 3.1.4 Drawing Essential Criteria Conclusions -- 3.2 Prior Pha Quality And Completeness -- 3.2.1 Application Of Analysis Method(S) -- 3.2.2 Level Of Detail And Accuracy Of The Core Analysis -- 3.2.3 Logic Errors And Inconsistencies In The Analysis -- 3.2.4 Failure To Document Hazards -- 3.2.5 Improper Application Of Risk Tolerance -- 3.2.6 Drawing Quality And Completeness Conclusions -- 3.3 Prior Pha Topics For Additional Evaluation -- 3.3.1 Status Of Prior Pha Recommendations.
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|a 3.3.2 Complementary Analyses And Supplemental Risk Assessments -- 3.3.3 Opportunity To Learn And Capture Information -- 3.3.4 Continuous Improvement -- 3.3.5 Pha Documentation Software Changes -- 3.3.6 Time Since The Previous Redo -- 3.4 Principles For Successful Prior Pha Evaluation -- 4 Evaluating Operating Experience Since The Prior Pha -- 4.1 Operating Experience Influence On Revalidation -- 4.2 Types Of Operating Experience That Should Be Considered -- 4.2.1 Moc And Pssr Records -- 4.2.2 Incident Reports -- 4.2.3 Routine Maintenance Records -- 4.2.4 Audit Results -- 4.2.5 Organizational Changes Not Addressed By Mocs -- 4.2.6 Metrics And Overall Performance -- 4.3 How Operating Experience Affects The Revalidation -- 4.4 Principles For Successful Operating Experience Evaluation -- 5 Selecting An Appropriate Pha Revalidation Approach -- 5.1 Revalidation Approaches -- 5.1.1 Update -- 5.1.2 Redo -- 5.1.3 Combining Update And Redo In A Revalidation -- 5.2 Selecting The Revalidation Options -- 5.2.1 Have The Requirements Changed Significantly? -- 5.2.2 Is The Prior Pha Deficient Or Unacceptable? -- 5.2.3 Are There Too Many Changes Or Significant Revelations In Operating Experience? -- 5.3 Principles For Successful Revalidation Approach Selection -- 6 Preparing For Pha Revalidation Meetings -- 6.1 Planning The Revalidation Meetings -- 6.1.1 Establishing The Revalidation Scope -- 6.1.2 Selecting Team Members -- 6.1.3 Estimating Schedule, Time, And Resources -- 6.2 Identifying And Collecting Information -- 6.2.1 Determining Information Requirements -- 6.2.2 Distributing Information -- 6.3 Reviewing And Preparing Information -- 6.3.1 Prior Pha Reports And Related Documentation -- 6.3.2 Prior Pha Recommendation Resolution Status -- 6.3.3 Moc And Pssr Records -- 6.3.4 Audit Results -- 6.3.5 Incident Reports -- 6.3.6 Current Piping And Instrument Diagrams.
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|a 6.3.7 Current Operating Procedures -- 6.3.8 Special Considerations For Complementary Analyses And Supplemental Risk Assessments -- 6.4 Principles For Successful Revalidation Preparation -- 7 Conducting Pha Revalidation Meetings -- 7.1 Applying Analysis Methodologies -- 7.1.1 Revalidation Of The Core Analysis -- 7.1.2 Revalidation Of Complementary Analyses -- 7.1.3 Revalidation Of Supplemental Risk Assessments -- 7.2 Facilitating Effective Revalidation Meetings -- 7.2.1 Team Composition -- 7.2.2 Meeting Kickoff -- 7.2.3 Meeting Productivity -- 7.3 Revalidation Meeting Conclusion -- 7.4 Principles For Successful Revalidation Meetings -- 8 Documenting And Following Up On A Pha Revalidation -- 8.1 Documentation Approaches -- 8.2 Report And Its Contents -- 8.3 Recommendations And Follow-Up -- 8.4 Records Retention And Distribution -- 8.5 Principles For Successful Documentation And Follow-Up -- References -- Appendices -- Appendix A Essential Criteria Checklist -- Appendix B Pha Quality And Completeness Checklist -- Appendix C Example Change Summary Worksheet -- Appendix D Checklist Of Process, Facility, And Human Factors Changes -- Appendix E Example Facility Siting Checklists -- Appendix F Example Human Factors Checklists -- Appendix G Example External Events Checklist -- Index
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|a "This book is derived from the experience of many companies in the chemical and hydrocarbon processing industries, and presents demonstrated, concise, and common sense approaches for a resource-effective revalidation of process hazard analyses (PHAs). It includes flowcharts, checklists, and worksheets that provide invaluable assistance to the revalidation process. The new edition, now as a guideline, provides a complete and thorough update of the first book and will provide much needed and requested guidance on PHA Revalidations including evaluating Prior PHA Studies, Identifying an Appropriate Revalidation Methodology, Preparing and Conducting the Revalidation Study Sessions, and Documenting the Revalidation Study"--
|c Provided by publisher.
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588 |
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|a Description based on online resource; title from digital title page (viewed on July 13, 2023).
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590 |
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|a Knovel
|b ACADEMIC - AICHE/CCPS (Premium Titles)
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650 |
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|a Chemical engineering
|x Safety measures.
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650 |
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|a Chemical engineering
|x Risk assessment.
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650 |
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|a Chemical plants
|x Inspection.
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650 |
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6 |
|a Génie chimique
|x Sécurité
|x Mesures.
|
650 |
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6 |
|a Génie chimique
|x Évaluation du risque.
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650 |
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|a Usines chimiques
|x Inspection.
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650 |
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|a Chemical processes
|x Safety measures
|2 fast
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655 |
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7 |
|a Handbooks and manuals
|2 fast
|
776 |
0 |
8 |
|i Print version:
|a American Institute of Chemical Engineers.
|t Guidelines for revalidating a process hazard analysi
|b Second edition.
|d Hoboken, NJ, USA : John Wiley & Sons, Inc. ; [New York, New York] : American Institute of Chemical Engineers, 2023
|z 9781119643609
|w (DLC) 2022052829
|
830 |
|
0 |
|a CCPS guidelines series.
|
856 |
4 |
0 |
|u https://appknovel.uam.elogim.com/kn/resources/kpGRPHAE03/toc
|z Texto completo
|
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|a Askews and Holts Library Services
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|a YBP Library Services
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