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Standard Guide for Record Keeping for Electrodialysis/Electrodialysis Reversal Systems (Withdrawn 2023)
Automaticky preložený názov:
Štandardné príručka pre vedenie evidencie elektrodializačného / elektrodialýzou Zúčtovanie systémy
NORMA vydaná dňa 1.6.2014
Označenie normy: ASTM D5131-90(2014)
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.6.2014
Kód tovaru: NS-29954
Počet strán: 3
Približná hmotnosť: 9 g (0.02 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Keywords:
desalination, electrodialysis, records, ICS Number Code 11.040.20 (Transfusion, Infusion)
Significance and Use | ||||||||||||
4.1 Proper operation and maintenance of an ED/EDR system and any associated pretreatment system are key factors in obtaining optimum performance. This guide provides the necessary input data for the evaluation of the performance of the ED/EDR system, the pretreatment system, and the mechanical equipment in the plant. 4.2 This guide is for general guidance only and must not be used in place of the operating manuals and manufacturer's recommendations for specific equipment or a specific application. 4.3 Site dependent, equipment design and regulatory requirement factors prevent specific recommendations for all record keeping. Thus, only general record keeping relating to operation and maintenance is covered by this guide. |
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1. Scope | ||||||||||||
1.1 This guide covers procedures for well defined record keeping for electrodialysis (ED) and electrodialysis reversal (EDR) systems. 1.2 This guide includes a start up report and record keeping for ED/EDR and pretreatment operating and maintenance data. 1.3 This guide is applicable to all waters but is not necessarily complete for waste waters. 1.4 This is a guide only and should not be construed as a complete delineation of all record keeping required for a specific application. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. |
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2. Referenced Documents | ||||||||||||
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