首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Headspace solid phase microextraction in the determination of pesticides in water samples from the Okavango Delta with gas chromatography-electron capture detection and time-of-flight mass spectrometry
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Headspace solid phase microextraction in the determination of pesticides in water samples from the Okavango Delta with gas chromatography-electron capture detection and time-of-flight mass spectrometry

机译:顶空固相微萃取-气相色谱-电子捕获检测和飞行时间质谱法测定奥卡万戈三角洲水样中的农药

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Headspace solid phase microextraction (HS-SPME) was optimized for the analysis of pesticides with gas chromatography electron capture detection (GC-ECD) and high-resolution mass spectrometry. Factors influencing the extraction efficiency such as fiber type, extraction mode and temperature, effect of ionic strength, stirring and extraction time were evaluated. The lowest pesticide concentrations that could be detected in spiked aliquots after HS-SPME-GC-ECD ranged from 0.0005 to 0.0032 mu g L-1. Consequently hexachlorobenzene, trans-chlordane, 4,4'-DDD and 4,4'-DDE were detected in water samples after HS-SPME at concentrations ranging from 2.4 to 61.4 mu g L-1 that are much higher than the 0.1 mu g L-1 maximum limit of individual organochlorine pesticides in drinking water set by the European Community Directive. The same samples were cleaned with ISOLUTE C-18 SPE sorbent with an optimal acetone-hexane (1:1 v/v) mixture for the elution of analytes. No pesticides were detected after SPE clean-up and pre-concentration. Precision for both methods was satisfactory with relative standard deviations less than 20%. This work demonstrated the superiority of HS-SPME as a sample clean-up and pre-concentration technique for pesticides in water samples as well as the need to identify and control point sources of pesticides.
机译:顶空固相微萃取(HS-SPME)经过优化,可通过气相色谱电子捕获检测(GC-ECD)和高分辨率质谱分析农药。评估了影响萃取效率的因素,例如纤维类型,萃取方式和温度,离子强度的影响,搅拌和萃取时间。 HS-SPME-GC-ECD后加标等分试样中可以检测到的最低农药浓度为0.0005至0.0032μg L-1。因此,HS-SPME后在水样品中检测到六氯苯,反氯丹,4,4'-DDD和4,4'-DDE的浓度范围为2.4至61.4μgL-1,远高于0.1μg。欧洲共同体指令设定的饮用水中单个有机氯农药的L-1最高限量。使用ISOLUTE C-18 SPE吸附剂和最佳丙酮/正己烷(1:1 v / v)混合物清洗相同样品,以洗脱分析物。 SPE净化和预浓缩后未检测到任何农药。两种方法的精密度均令人满意,相对标准偏差小于20%。这项工作证明了HS-SPME作为水样品中农药的样品净化和预浓缩技术的优越性,以及确定和控制农药点源的需求。

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