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Issues for Storing Alternative Fuels

机译:储存替代燃料的问题

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Experiments were designed to answer the following questions: Are issues for storing alternative fuels in contact with natural seawater different from those experienced with petroleum-based fuels? Does initial oxygen concentration in the seawater and fuel phases affect biodegradation? What roles do the differences in seawater compositions (chemical and microbiological) play in the degradation of alternative fuels and the resulting corrosion? Under typical conditions, seawater in contact with petroleum-based (JP5JP5, F76 and ultra-low sulphur diesel) and alternative (camelina-derived JP5, algal-derived F76 and fatty acid methyl ester [FAME]) fuels stored with uncoated carbon steel became anaerobic within days due to oxygen consumption by corrosion reactions and aerobic respiration. Sulphides, produced by anaerobic sulphate-reducing bacteria, and chlorides were co-located in corrosion products in both the seawater and fuel phases. In general, higher sulphide levels were associated with alternative fuels when compared with their petroleum-based counterpart. Transient oxygen influenced both metabolic degradation pathways and resulting metabolites. Catechols, indicative of aerobic degradation, and typically aerobic bacteria persisted after three-month exposures. Detection of catechols suggested that initial exposure to oxygen resulted in their formation. Transient exposure to oxygen resulted in higher proportions of Firmicutes, Deltaproteobacteria (primarily sulphate-reducing bacteria), Chloroflexi, and Lentisphaerae in seawaters exposed to fuels than the original seawater. Relative proportions of sequences affiliated with these bacterial groups varied with fuel. Despite the dominance of characteristically anaerobic taxa, sequences for the key enzyme of an aerobic hydrocarbon-degradation enzyme (alkane monooxygenase) were obtained following PCR amplification. Two different seawaters, Coastal Key West, FL, and Persian Gulf seawaters, representing an oligotrophic and a more organic- and inorganic mineral-rich environment, were used to evaluate the effect of seawater properties on biodegradation and corrosion. The original microflora of the two seawaters were similar with respect to major taxonomic groups but with markedly different species. After exposure to FAME diesel, the microflora of the waters changed dramatically, with Clostridiales (Firmicutes) becoming dominant in both seawaters. Despite low numbers of sulphate reducing bacteria in the original seawaters and after fuel exposure, sulphide levels and corrosion increased markedly due to microbial sulphate reduction in the presence of Key West seawater, but to a lesser extent with Persian Gulf seawater.
机译:实验旨在回答以下问题:是储存与自然海水接触的替代燃料的问题,与石油型燃料有关的自然海水有所不同吗?初始氧浓度在海水和燃料阶段是否影响生物降解?在替代燃料的降解和所产生的腐蚀中,海水组合物(化学和微生物)的差异在替代燃料的降解中作出差异?在典型的条件下,与石油(JP5JP5,F76和超低硫柴油)和替代(Camelina-errived JP5,藻类衍生的F76和脂肪酸甲基酯[FAME])燃料的海水变得燃料由于腐蚀反应和有氧呼吸而在几天内厌氧。通过厌氧硫酸盐降低细菌产生的硫化物和氯化物在海水和燃料相中共同位于腐蚀产物中。通常,与基于石油的对应物相比,较高的硫化物水平与替代燃料相关。瞬时氧气影响代谢降解途径和结果代谢物。儿茶酚,指示有氧降解,通常在三个月暴露后持续有氧细菌。儿茶酚的检测表明,初始暴露于氧气导致其形成。暂时暴露于氧气导致较高比例的较高比例,Deltaproteobacteria(主要是硫酸盐还原细菌),氯昔克氏菌和在暴露于燃料的海水中,而不是原始海水。与这些细菌基团相关的序列的相对比例随燃料而变化。尽管具有特征性的厌氧分类群的优势,但在PCR扩增后获得了一种有氧烃 - 降解酶(烷烃单氧化酶)的关键酶的序列。两种不同的海水,沿海基韦斯特,佛罗里达州和波斯湾海洋水域,代表寡营养和更具有机和无机矿物质的环境,用于评估海水性质对生物降解和腐蚀的影响。两个海洋水域的原始缩略量与主要的分类学群体相似,但具有明显不同的物种。暴露于柴油柴油后,水的微生物群急剧变化,梭太型(迫使)在两海洋中变得占主导地位。尽管原有的海洋水域中硫酸盐的硫酸盐较少,但在燃料暴露后,由于基韦斯海水的存在微生物硫酸盐降低,硫化物水平和腐蚀显着增加,但在较小程度上与波斯湾海水较小。

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