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Standard Practice for Evaluation of Antimicrobials in Liquid Fuels Boiling Below 390°;C
Automatically translated name:
Standard Practice for Evaluation of Antimicrobials in Liquid Fuels Boiling Below 390°C
STANDARD published on 1.11.2005
Designation standards: ASTM E1259-05
Note: WITHDRAWN
Publication date standards: 1.11.2005
SKU: NS-41046
The number of pages: 5
Approximate weight : 15 g (0.03 lbs)
Country: American technical standard
Category: Technical standards ASTM
Keywords:
antimicrobials, aviation fuels, biodeterioration, diesel, distillate fuels, gasoline, gas-turbine fuels, marine fuels, microbially-induced deterioration
Significance and Use | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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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