ASTM D7978-14由美国材料与试验协会 US-ASTM 发布于 2014。
5.1 This test method is intended to provide a tool for assessing whether fuel storage and distribution facilities or end user fuel tanks are subject to microbial growth and alert fuel suppliers or users to the potential for fuel quality or operational problems and/or the requirement for preventative or remedial measures.
5.2 This test method detects numbers of microbial colony forming units (CFU), the same detection parameter used in the laboratory standard procedures Practice D6974 and IP 385. However, whereas Practice D6974 and IP 385 provide separate assessment of numbers of viable aerobic bacteria CFU and numbers of viable fungal CFU, this test method provides a combined total count of viable aerobic bacteria and fungal CFU.
5.3 This test method is designed to detect a recognized group of microorganisms of significance in relation to contamination of distillate fuels, but it is recognized that microbiological culture techniques do not detect all microorganisms that can be present in a sample. Culturability is affected primarily by the ability of captured microbes to proliferate on the growth medium provided, under specific growth conditions. Consequently, a proportion of the active or inactive microbial population present in a sample can be viable but not detected by any one culture test.7 In this respect, the test is indicative of the extent of microbial contamination in a sample ,and it is assumed that when a fuel sample is significantly contaminated, some of the dominant microbial species present will be quantifiably detected, even if not all species present are culturable.
5.4 Many samples from fuel systems can be expected to contain a low level of “background” microbial contamination, which is not necessarily of operational significance. The minimum detection level of this test method is determined by the volume of specimen tested and is set such that microbial contamination will generally only be detected when it is at levels indicative of active proliferation.
5.5 The test will detect culturable bacteria and fungi that are metabolically active and dormant fungal spores. Presence of fungal spores in a fuel sample can be indicative of active microbial proliferation within a fuel tank or system, but at a point distant from the location sampled. Active microbial growth only occurs in free water, and this can be present only as isolated pockets at tank or system low points. Because fungal spores are more hydrophobic than active cells and fungal material (mycelium), they disperse more readily in fuel phase and are thus more readily detected when low points cannot be directly sampled and only fuel phase is present in samples.
5.6 This test method can determine whether microbial contamination in samples drawn from fuel tanks and systems is absent or present at light, moderate, and heavy levels.
5.7 The categorization of light, moderate, and heavy levels of contamination will depend on the fuel type, the sampling location, the facility sampled, and its specific operating circumstances.
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⑥ 使用新型生物载体,载体用于好氧,厌氧和缺氧段,硝化和反硝化细菌通过控制混合混合物的回流,在同一结构中培养,同时硝化和反硝化成功实现。提高氨氮去除率可提高处理磷的能力。⑦ 同时,由于载体外流速快,曝气量大,整个池处于有氧状态,但载体内会发生缺氧和厌氧反应。这种厌氧状态被整个好氧状态包围,不产生异味,从根本上解决了传统工艺。有气味问题。...
⑥ 使用新型生物载体,载体用于好氧,厌氧和缺氧段,硝化和反硝化细菌通过控制混合混合物的回流,在同一结构中培养,同时硝化和反硝化成功实现。提高氨氮去除率可提高处理磷的能力。⑦ 同时,由于载体外流速快,曝气量大,整个池处于有氧状态,但载体内会发生缺氧和厌氧反应。这种厌氧状态被整个好氧状态包围,不产生异味,从根本上解决了传统工艺。有气味问题。...
⑥ 使用新型生物载体,载体用于好氧,厌氧和缺氧段,硝化和反硝化细菌通过控制混合混合物的回流,在同一结构中培养,同时硝化和反硝化成功实现。提高氨氮去除率可提高处理磷的能力。⑦ 同时,由于载体外流速快,曝气量大,整个池处于有氧状态,但载体内会发生缺氧和厌氧反应。这种厌氧状态被整个好氧状态包围,不产生异味,从根本上解决了传统工艺。有气味问题。...
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