首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >In-capillary preconcentration of pirimicarb and carbendazim with a monolithic polymeric sorbent prior to separation by CZE.
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In-capillary preconcentration of pirimicarb and carbendazim with a monolithic polymeric sorbent prior to separation by CZE.

机译:在用CZE分离之前,用整体式聚合物吸附剂在毛细管中对吡虫威和多菌灵进行预浓缩。

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摘要

CZE was assayed for the separation of carbamate pesticides susceptible to protonation (Pirimicarb, Carbendazim). Different electrophoretic media with high organic contents were explored, adequate separation and resolution being achieved when a BGE based on ACN with acetic acid in the presence of SDS as an ionic additive was used. With a view to increasing the sensitivity of the method, an in-capillary SPE step prior to the electrophoretic separation was developed. We employed a monolithic polymer formed in situ within the capillary as a medium for analyte retention. The synthesized monolithic bed exhibited high porosity and allowed samples to be loaded at flow rates of about 65 muL/min by applying a pressure of 12 bar. A 5-cm length of monolithic sorbent was used to preconcentrate the target analytes from aqueous samples. The analytes retained were eluted from the polymeric phase directly in the separation capillary with the same electrophoretic medium used for their further separation by CZE. For a 15-min preconcentration time, the in-line SPE-CZE approach proposed here permitted the determination of these pesticides in drinking water at a concentration level of 0.1 mug/L, as demanded by current EU legislation.
机译:测定了CZE的分离程度,使易质子化的氨基甲酸酯农药(吡虫威,多菌灵)分离。探索了具有高有机含量的不同电泳介质,当在SDS作为离子添加剂存在下使用基于ACN和乙酸的BGE时,可以实现足够的分离和分离。为了提高该方法的灵敏度,开发了电泳分离之前的毛细管内SPE步骤。我们采用在毛细管内原位形成的整体式聚合物作为分析物保留的介质。合成的整体床显示出高孔隙率,并通过施加12 bar的压力使样品以约65μL/ min的流速上样。使用5 cm长的整体式吸附剂从水溶液样品中预浓缩目标分析物。保留的分析物直接用与通过CZE进行进一步分离所用的相同电泳介质在分离毛细管中直接从聚合物相中洗脱出来。在15分钟的预浓缩时间内,这里提出的在线SPE-CZE方法允许按照欧盟现行法规的要求,以0.1杯/升的浓度测定饮用水中的这些农药。

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