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Method for the simultaneous determination of monoaromatic and polycyclic aromatic hydrocarbons in industrial effluents using dispersive liquid-liquid microextraction with gas chromatography-mass spectrometry

机译:用气相色谱 - 质谱法同时使用分散液 - 液体微萃取在工业液体中单芳族和多环芳烃的方法

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摘要

We present a new method for simultaneous determination of 22 monoaromatic and polycyclic aromatic hydrocarbons in postoxidative effluents from the production of petroleum bitumen using dispersive liquid-liquid microextraction coupled to gas chromatography and mass spectrometry. The eight extraction parameters including the type and volume of extraction and disperser solvent, pH, salting out effect, extraction, and centrifugation time were optimized. The low detection limit ranging from 0.36 to 28 mu g/L, limit of quantitation (1.1-84 mu g/L), good reproducibility, and wide linear ranges, as well as the recoveries ranging from 71.74 to 114.67% revealed that the new method allows the determination of aromatic hydrocarbons at low concentration levels in industrial effluents having a very complex composition. The developed method was applied to the determination of content of mono-and polycyclic aromatic hydrocarbons in samples of raw postoxidative effluents in which 15 compounds were identified at concentrations ranging from 1.21 to 1017.0 mu g/L as well as in effluents after chemical treatment.
机译:我们使用分散液 - 液体微萃取与气相色谱法和质谱法同时测定出晚期氧化污水中22种单芳族和多环芳烃的新方法。优化了八个提取参数,包括提取和分散器溶剂,pH,盐洗效应,提取和离心时间的类型和体积。低检测限度范围为0.36至28μg/ l,量子限制(1.1-84μg/ l),良好的再现性和宽线性范围,以及从71.74到114.67%的回收率显示新的方法允许在具有非常复杂的组合物的工业污水中测定低浓度水平的芳烃。将开发的方法应用于原料发达氧化污水样品中单环状芳烃含量的测定,其中在化学处理后,以1.21至1017.0μmg/ l以及流出物的浓度鉴定了15种化合物。

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