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首页> 外文期刊>Journal of separation science. >Simultaneous extraction and preconcentration of aniline, phenol, and naphthalene using magnetite-graphene oxide composites before gas chromatography determination
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Simultaneous extraction and preconcentration of aniline, phenol, and naphthalene using magnetite-graphene oxide composites before gas chromatography determination

机译:气相色谱法测定前使用磁铁矿-氧化石墨烯复合材料同时萃取和预浓缩苯胺,苯酚和萘

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摘要

The coextraction of acidic and basic compounds from different mediums is a significant concept in sample preparation. In this work, simultaneous extraction of acidic, basic, and neutral analytes in a single step was carried out for the first time. This procedure employed the dispersive solid-phase microextraction of analytes with magnetic graphene oxide (graphene oxide/Fe3O4) sorbent followed by gas chromatography with flame ionization detection. After the adsorption of analytes by vortexing and decantation of the supernatant with a magnet, the sorbent was eluted with acetonitrile/methanol (2: 1) mixture. The parameters affecting the extraction efficiency were optimized and obtained as follows: sorbent amount 60 mg, desorption time 1 min, extraction time 5 min, pH of the sample 7, sample volume 20 mL, and elution solvent volume 0.3 mL. Under the optimum conditions, linear dynamic ranges were achieved in the range of 0.5-4, 0.25-4, and 0.25-2 mu g/mL and limits of detection were 0.341, 0.110, and 0.167 mu g/mL for aniline, phenol, and naphthalene, respectively. The relative standard deviations were in the range of 3.3-5.7% in eight repeated extractions. Finally, the applicability of the method was evaluated by the extraction and determination of analytes in stream water and drinking water samples and satisfactory results were obtained.
机译:从不同介质中共萃取酸性和碱性化合物是样品制备中的重要概念。在这项工作中,首次在一个步骤中同时进行了酸性,碱性和中性分析物的提取。该程序采用了磁性氧化石墨烯(氧化石墨烯/ Fe3O4)吸附剂对分析物进行分散固相微萃取,然后进行气相色谱和火焰离子化检测。在通过涡旋和倾析上清液用磁体吸附分析物之后,用乙腈/甲醇(2:1)混合物洗脱吸附剂。对影响萃取效率的参数进行了优化,并获得了以下参数:吸附剂量60 mg,解吸时间1 min,萃取时间5 min,样品7的pH,样品体积20 mL,洗脱溶剂体积0.3 mL。在最佳条件下,线性动态范围为0.5-4、0.25-4和0.25-2μg / mL,苯胺,苯酚,和萘。在八次重复萃取中,相对标准偏差在3.3-5.7%的范围内。最后,通过提取和测定溪流水和饮用水样品中的分析物来评价该方法的适用性,并获得满意的结果。

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