利用萃取冷冻分析物的气相色谱-质谱法测定水中的多氯联苯

T. Chervonnaya, T. N. Musorina, Z. Temerdashev, V. N. Bekhterev, I. Korpakova
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引用次数: 0

摘要

利用离心力(EFC)作用下的萃取冷冻法浓缩分析物的方法,开发了一种测定水中多氯联苯(PCBs)的方法。采用三因素盒-贝肯设计的分析物萃取数学模型表明,萃取混合物中乙腈的含量是一个重要因素,而多氯联苯的氯化程度和分析物的浓度则是不重要的参数。通过对模型表面积的分析,确定了乙腈浓度的最佳范围,即介于 14% 和 21% 之间。萃取混合物中的乙腈含量为 15%时,在广泛的分析物浓度范围内(1.0 - 5000 纳克/升),7 种不同的多氯联苯的萃取效率最高(>92%)。重复性和再现性的相对标准偏差分别为 4.2%至 6.8%和 5.3%至 8.1%,分析测定的准确度为 10%至 15%。乙腈萃取液中未萃取石油烃类,不会干扰多氯联苯的测定,因此检测器的工作时间更长,灵敏度也不会降低。多环芳烃和氯化农药的共萃取不会影响从水中萃取多氯联苯(95-100%),也不会影响测定程序的计量指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GC-MS determination of polychlorinated biphenyls in water using extractive freezing-out of analytes
A method for determining polychlorinated biphenyls (PCBs) in water using the method of concentrating analytes through extractive freezing-out under the effect of a centrifugal forces (EFC) has been developed. A mathematical model for analyte extraction using a three-factor Box-Behnken design demonstrated that the content of acetonitrile in the extraction mixture is a significant factor, whereas the degree of PCBs chlorination and the concentration of analytes are insignificant parameters. Analysis of the surface area of the model allowed the determination of the optimal range of the acetonitrile concentration, which fell between 14 and 21%. A 15% content of acetonitrile in the extraction mixture provided maximum extraction efficiency for 7 different PCBs (>92%) across a wide range of analyte concentrations (1.0 – 5000 ng/liter). The relative standard deviations in the repeatability and reproducibility range from 4.2 to 6.8% and 5.3 to 8.1%, respectively, the accuracy of analyte determination being 10 – 15%. Petroleum hydrocarbons were not extracted into the acetonitrile extract and did not interfere with the determination of PCBs, which provided longer operation of the detector without any loss in the sensitivity. Co-extraction of polycyclic aromatic hydrocarbons and chlorinated pesticides did not affect the extraction of PCBs from water (95 – 100%) and did not touch on the metrological indicators of the determination procedure.
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