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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Trace analysis of polychlorinated dibenzo-p-dioxins, dibenzofurans and WHO polychlorinated biphenyls in food using comprehensive two-dimensional gas chromatography with electron-capture detection
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Trace analysis of polychlorinated dibenzo-p-dioxins, dibenzofurans and WHO polychlorinated biphenyls in food using comprehensive two-dimensional gas chromatography with electron-capture detection

机译:使用具有电子捕获检测功能的全面二维气相色谱法对食品中的多氯二苯并对二恶英,二苯并呋喃和WHO多氯联苯进行痕量分析

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摘要

Trace analysis of 2,3,7,8-polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs) and the 12 WHO-PCBs (four non-ortho and eight mono-ortho congeners that have been assigned toxic equivalence factors, TEFs, by the World Health Organisation) was conducted by comprehensive two-dimensional gas chromatography with a micro electron-capture detector (GC x GC-mu ECD). Four food matrices (fish oil from herring, spiked cows' milk, vegetable oil and an eel extract) were analysed by two GC x GC laboratories, and four GC-HRMS laboratories generated reference values. The two GC x GC laboratories used different column combinations for separating the target analytes. For the first dimension, non-polar DB-XLB and VF-1 columns were used, and for the second dimension, an LC-50 liquid crystalline column with unique selectivity for planar compounds. The congener-specific and total toxic equivalence (TEQ) data obtained using DB-XLB x LC-50 were in good agreement with results obtained by the GC-HRMS laboratories. The WHO-PCB data obtained with the VF-1 x LC-50 combination was also good, but the PCDD/F concentrations were sometimes overestimated due to matrix interferences. GC x GC-mu ECD using DB-XLB x LC-50 seems to fulfil the European Community requirements of a screening method for PCDD/F and WHO-PCB TEQ in food. (c) 2004 Elsevier B.V. All rights reserved.
机译:痕量分析2,3,7,8-多氯二苯并对二恶英(PCDD),二苯并呋喃(PCDF)和12种WHO-PCB(已被指定有毒当量因子的四个非邻位同源物和八个单邻位同源物,由世界卫生组织(TEF)进行的二维二维气相色谱仪带有微电子捕获检测器(GC x GC-mu ECD)。由两个GC x GC实验室分析了四个食品基质(鲱鱼鱼油,加牛奶的牛乳,植物油和鳗鱼提取物),四个GC-HRMS实验室生成了参考值。两个GC x GC实验室使用不同的色谱柱组合来分离目标分析物。对于第一维,使用非极性DB-XLB和VF-1色谱柱,对于第二维,使用LC-50液晶色谱柱,对平面化合物具有独特的选择性。使用DB-XLB x LC-50获得的同类物特异性和总毒性当量(TEQ)数据与GC-HRMS实验室获得的结果高度吻合。用VF-1 x LC-50组合获得的WHO-PCB数据也不错,但由于基质干扰,有时会高估PCDD / F的浓度。使用DB-XLB x LC-50的GC x GC-mu ECD似乎可以满足欧洲共同体对食品中PCDD / F和WHO-PCB TEQ筛选方法的要求。 (c)2004 Elsevier B.V.保留所有权利。

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