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ASTM E1259-05
Standard Practice for Evaluation of Antimicrobials in Liquid Fuels Boiling Below 390°;C
Automaticky preložený názov:
Štandardná prax pre hodnotenie antimikrobiálnych látok u kvapalných palív varu Pod 390 ° C
NORMA vydaná dňa 1.11.2005
Informácie o norme:
Označenie normy: ASTM E1259-05
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.11.2005
Kód tovaru: NS-41046
Počet strán: 5
Približná hmotnosť: 15 g (0.03 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Anotácia textu normy ASTM E1259-05 :
Keywords:
antimicrobials, aviation fuels, biodeterioration, diesel, distillate fuels, gasoline, gas-turbine fuels, marine fuels, microbially-induced deterioration
Doplňujúce informácie
| Significance and Use | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Guide D 6469 details the types of problems associated with uncontrolled microbial growth in fuels and fuel systems. Treatment with effective antimicrobial agents is one element of contamination control strategy. The procedure should be used to evaluate the relative efficacy of microbicides in liquid fuels boiling below 390°C. The effect of environmental conditions, such as a variety of fuel additives, metal surfaces, and climatology, are variables that can be included in specific tests using this protocol. This practice addresses product performance issues only. Regulatory Agencies restrict and control the use of both pesticides (in the U.S.: 40 CFR 152) and fuel additives (40 CFR 79). Regardless of performance in this method, antimicrobials must only be used in compliance with applicable regulations. Specific industries, for example, the aviation industry, may place further restrictions on chemicals used for fuel treatment. |
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| 1. Scope | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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1.1 This practice is designed to evaluate antimicrobial agents for the prevention of microbially influenced deterioration of liquid fuels (as defined by Specification D 396, D 910, D 975, D 1655, D 2069, D 2880, D 3699, D 4814, D 6227, and D 6751), system deterioration, or both. 1.2 Knowledge of microbiological techniques is required for these procedures. 1.3 It is the responsibility of the investigator to determine whether Good Laboratory Practice (GLP) is required and to follow them where appropriate (40 CFR, 160), or as revised. 1.4 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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