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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Polymer-coated magnetic nanospheres for preconcentration of organochlorine and pyrethroid pesticides prior to their determination by gas chromatography with electron capture detection
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Polymer-coated magnetic nanospheres for preconcentration of organochlorine and pyrethroid pesticides prior to their determination by gas chromatography with electron capture detection

机译:聚合物包覆的磁性纳米球用于有机氯和拟除虫菊酯农药的预浓缩,然后通过电子捕获检测气相色谱法测定

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摘要

Magnetic polymer nanospheres were prepared and used as adsorbents for the extraction of organochlorine and pyrethroid pesticides from water samples. The adsorbents were synthesized by miniemulsion polymerization of N-vinylimidazole and divinylbenzene and simultaneous encapsulation of oleic acid-coated Fe3O4 nanoparticles. Following desorption with ethyl acetate, the target analytes beta-hexachlorocyclohexane, delta-hexachlorocyclohexane, p,p'-DDE, heptachlor, trans-chlordan, cis-chlordan, bifenthrin, beta-cypermethrin, delta-methrin, lambda-cyhalothrin and esfenvalerate were determined by gas chromatography with electron capture detection. Desorption conditions, extraction times and sample volume were screened by Plackett-Burman design and optimized by Box-Behnken design. Under the optimum conditions, the organochlorines can be quantified in the 20 to 400 ng L-1 concentration range, and the pyrethroids in the 400 to 4000 ng L-1 concentration range. The recoveries of organochlorines and pyrethroids from spiked real water samples are between 77.6 and 97.3 %, with relative standard deviations between 0.9 and 10.0 %. The method for magnetic solid phase extraction described here is fast, simple and friendly to the environment.
机译:制备了磁性聚合物纳米球,并将其用作吸附剂,用于从水样中提取有机氯和拟除虫菊酯类农药。通过N-乙烯基咪唑和二乙烯基苯的细乳液聚合并同时包封油酸包覆的Fe3O4纳米粒子,可以合成吸附剂。用乙酸乙酯解吸后,目标分析物为β-六氯环己烷,δ-六氯环己烷,p,p'-DDE,七氯,反式氯丹,顺式氯丹,联苯菊酯,β-氯氰菊酯,δ-甲基菊酯,λ-氟氯氰菊酯和艾芬戊酸酯用电子捕获检测气相色谱法测定。解吸条件,提取时间和样品量通过Plackett-Burman设计进行筛选,并通过Box-Behnken设计进行优化。在最佳条件下,有机氯的定量范围为20至400 ng L-1,拟除虫菊酯的定量范围为400至4000 ng L-1。加标的真实水样中有机氯和拟除虫菊酯的回收率在77.6至97.3%之间,相对标准偏差在0.9至10.0%之间。本文所述的磁性固相萃取方法快速,简单且对环境友好。

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