首页> 外文期刊>Journal of Hazardous Materials >Applicability Of Cloud Point Extraction Coupled With Microwave-assisted Back-extraction To The Determination Of Organophosphorous Pesticides In Human Urine By Gas Chromatography With Flame Photometry Detection
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Applicability Of Cloud Point Extraction Coupled With Microwave-assisted Back-extraction To The Determination Of Organophosphorous Pesticides In Human Urine By Gas Chromatography With Flame Photometry Detection

机译:浊点萃取-微波辅助反萃取-气相色谱-火焰光度法测定人尿中有机磷农药的适用性

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摘要

A procedure for the determination of organophosphorous pesticides (OPPs) - phorate, diazinon, parathion-methyl, fenthion and quinalphos - in human urine was developed using the cloud point extraction of nonionic surfactant (Triton X-114) coupled with microwave-assisted back-extraction prior to gas chromatography with flame photometry detection (GC-FPD) analysis. The upper organic solution obtained from back-extraction was centrifugated simply for further cleanup for the sake of automatic injection. A preconcentration factor of 50 was obtained for these five OPPs extracted from only 10 mL of a sample. The limits of detection (LODs) were 0.07 ng mL~(-1) for phorate, fenthion and quinalphos, 0.04 ng mL~(-1) for diazinon and 0.08 ng mL~(-1) for parathion-methyl. The limits of quantification (LOQs) were 0.21,0.12,0.24, 0.21 and 0.21 ng mL~(-1), respectively. Accuracy of the method was evaluated by bias, which ranged from +6.85 to -14.68%. Precision was also good; the relative standard deviations (R.S.D.S) were less than 9%. The method showed to be potential for biological monitoring.
机译:使用非离子表面活性剂(Triton X-114)的浊点萃取结合微波辅助反萃取技术,开发了一种测定人尿中有机磷农药(OPP)的方法-磷酸根,二嗪农,甲基对硫磷,倍硫磷和喹啉。气相色谱法进行火焰光度检测(GC-FPD)分析之前进行萃取。为了自动进样,简单地将从反萃取中获得的上层有机溶液进行离心,以进一步净化。仅从10 mL样品中提取的这五种OPP的预浓缩系数为50。甲酸酯,磷硫磷和喹硫磷的检出限(LODs)为0.07 ng mL〜(-1),二嗪农为0.04 ng mL〜(-1),对硫磷甲基为0.08 ng mL〜(-1)。定量限(LOQs)分别为0.21,0.12,0.24,0.21和0.21 ng mL〜(-1)。通过偏差评估方法的准确性,偏差范围为+6.85至-14.68%。精度也不错;相对标准偏差(R.S.D.S)小于9%。该方法显示出对生物监测的潜力。

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