首页> 外文会议>2009 ISEST;International symposium on environmental science and technology >Occurrence and Determination of Volatile Fatty Acids in Wastewater of Different Origin
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Occurrence and Determination of Volatile Fatty Acids in Wastewater of Different Origin

机译:不同来源废水中挥发性脂肪酸的发生与测定

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Volatile fatty acids (VFAs) are aliphatic monocarboxylic acids containing from 2 to 8 carbon atoms. They are formed in anaerobic biodegradation of larger molecules and play an important role in biological wastewater treatment. They should be monitored in raw waste water, at different stages of its treatment and in treated wastewater. Usually, the determination of VFAs in environmental aqueous samples is preceded by pre-treatment based on VFA selective isolation by means of distillation, solvent extraction, solid phase microextraction, or gas extraction. For individual VFAs determination in the extracts, separation techniques, most often gas chromatography, are employed. In this work, extraction of selected C2-C8 VFAs with methyl-tert-butyl ether (LLE) from aqueous samples was tested and the separation and identification of VFAs in the extracts, by gas chromatography coupled with mass spectrometry (GC-MS) was studied. Open tubular capillary columns coated with Rtx-624 (crossbond 6% cyanopropylphenyl –94% dimethyl polysiloxane)and Stabilwax-DA (crossbond polyethylene glycol treated with nitroterephtalic acid) were used. The limits of quantitation of LLE-GC-MS procedure were on the level of 0.1 to 0.5 mg L-1. Unfortunately, for very “dirty” real samples containing many interfering substances some analyte acids could have been quantitatively determined at higher concentrations. Real samples of municipal raw and treated wastewater were successfully analysed. Dominant in all the samples was acetic acid.
机译:挥发性脂肪酸(VFA)是含有2至8个碳原子的脂肪族一元羧酸。它们在较大分子的厌氧生物降解中形成,并在生物废水处理中起重要作用。应在原废水,废水处理的不同阶段以及经过处理的废水中对它们进行监测。通常,在确定环境水性样品中的VFA之前,需要先进行基于VFA选择性分离的预处理,该方法通过蒸馏,溶剂萃取,固相微萃取或气体萃取进行。为了确定提取物中的各个VFA,采用了分离技术,通常是气相色谱法。在这项工作中,测试了用甲基叔丁基醚(LLE)从水性样品中提取选定的C2-C8 VFA的方法,并通过气相色谱-质谱联用(GC-MS)对提取物中的VFA进行了分离和鉴定。研究过。使用涂有Rtx-624(6%的氰基丙基苯基交联剂–94%的二甲基聚硅氧烷)和Stabilwax-DA(用硝基对苯二甲酸对交联的聚乙二醇)包被的开放式管状毛细管柱。 LLE-GC-MS方法的定量限为0.1至0.5 mg L-1。不幸的是,对于含有许多干扰物质的非常“肮脏”的真实样品,某些分析物酸原本可以在较高浓度下定量测定的。成功分析了市政原水和处理过的废水的真实样品。在所有样品中占主导地位的是乙酸。

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