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首页> 外文期刊>Analytica chimica acta >Comparison of silica and proous graphitic carbon as solid-phase extraction materials for the analysis of cationic herbicides in water by liquid chromatography and capillary electrophoresis
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Comparison of silica and proous graphitic carbon as solid-phase extraction materials for the analysis of cationic herbicides in water by liquid chromatography and capillary electrophoresis

机译:液相色谱和毛细管电泳法分析二氧化硅和粗石墨碳作为固相萃取材料用于水中阳离子除草剂的分析

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摘要

Preconcentration methods for the analysis of paraquat (PQ), idquat (DQ) and difenzoquat (DF) in water samples by solid-phase extraction (SPE) with silica and porous graphitic carbon (PGC) were evaluated. The breakthrough volumes of three quaternary ammonium herbicides were calculated in order to compare the loading capacity of both sorbents. They were determined by capillary electrophoresis (CE) and ion-pair reversed-phase liquid chromatography (LC) with UV detection. The recoveries were determined by spiking tap and river waters. Although the data showed that both sorbents were able to preconcentrate the cationic herbicides using CE and LC as separation and quantification techniques, silica was inappropriate for the CE determination of DF because marked distortions in the base line occurred. The best results were obtained for PGC with both separation techniques, which gave recoveries ranging from 6 to 90% and standard deviations between 4 and 10%. Practical detection limits (LODs) with LC were about 0.2 #mu#g l~(-1) and were one order of magnitude higher with CE.
机译:评估了通过硅胶和多孔石墨碳(PGC)固相萃取(SPE)分析水样品中百草枯(PQ),异丙草胺(DQ)和敌苯甲草胺(DF)的预富集方法。计算了三种季铵盐除草剂的突破体积,以比较两种吸附剂的负载量。它们是通过毛细管电泳(CE)和离子对反相液相色谱(LC)进行紫外线检测来测定的。通过加水龙头和河水来确定回收率。尽管数据表明两种吸附剂均能够使用CE和LC作为分离和定量技术对阳离子除草剂进行预浓缩,但二氧化硅不适合用于DF的CE测定,因为基线发生了明显的扭曲。两种分离技术均能使PGC获得最佳结果,其回收率范围为6%至90%,标准偏差为4%至10%。 LC的实际检测限(LOD)约为0.2#mu#g l〜(-1),而CE则高出一个数量级。

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