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  2. Hazard and operability study - Wikipedia

    en.wikipedia.org/wiki/Hazard_and_operability_study

    For example, a prudent designer will have allowed for foreseeable variations within the process, creating a larger design envelope than just the basic requirements, and the HAZOP will be looking at ways in which this might not be sufficient. A common use of the HAZOP is relatively early through the detailed design of a plant or process.

  3. Safety instrumented system - Wikipedia

    en.wikipedia.org/wiki/Safety_instrumented_system

    The PHA is in turn based on a hazard identification exercise. In the process industries (oil and gas production, refineries, chemical plants, etc.), this exercise is usually a hazard and operability study (HAZOP). The HAZOP usually identifies not only the process hazards of a plant (such as release of hazardous materials due to the process ...

  4. Layers of protection analysis - Wikipedia

    en.wikipedia.org/wiki/Layers_of_protection_analysis

    Layers of protection analysis (LOPA) is a technique for evaluating the hazards, risks and layers of protection associated with a system, such as a chemical process plant. . In terms of complexity and rigour LOPA lies between qualitative techniques such as hazard and operability studies (HAZOP) and quantitative techniques such as fault trees and event trees.

  5. Process hazard analysis - Wikipedia

    en.wikipedia.org/wiki/Process_Hazard_Analysis

    There are several methodologies that can be used to conduct a PHA, including checklists, hazard identification (HAZID) reviews, what-if reviews and SWIFT, hazard and operability studies (HAZOP), failure mode and effect analysis (FMEA), etc. PHA methods are qualitative or, at best, semi-quantitative in nature.

  6. Hazard analysis - Wikipedia

    en.wikipedia.org/wiki/Hazard_analysis

    Hazard and operability study (HAZOP) – Study of risks in a plan or operation; Layers of protection analysis (LOPA) – Technique for evaluating the hazards, risks and layers of protection of a system; Medical Device Risk Management - ISO 14971 – ISO standard

  7. Safety integrity level - Wikipedia

    en.wikipedia.org/wiki/Safety_integrity_level

    A device or system must meet the requirements for both categories to achieve a given SIL. The SIL requirements for hardware safety integrity are based on a probabilistic analysis of the device. In order to achieve a given SIL, the device must meet targets for the maximum probability of dangerous failure and a minimum safe failure fraction.