首页> 外文期刊>Journal of separation science. >Extraction of hydroxyaromatic compounds in river water by liquid-liquid-liquid microextraction with automated movement of the acceptor and the donor phase
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Extraction of hydroxyaromatic compounds in river water by liquid-liquid-liquid microextraction with automated movement of the acceptor and the donor phase

机译:液-液-液微萃取在受体和施主相自动移动下萃取河水中的羟基芳族化合物

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Liquid-liquid-liquid microextraction with automated movement of the acceptor and the donor phase technique is described for the extraction of six hydroxyaromatic compounds in river water using a disposable and ready to use hollow fiber. Separation and quantitative analyses were performed using LC with UV detection at 254 nm. Analytes were extracted from the acidified sample solution (donor phase) into the organic solvent impregnated in the pores of the hollow fiber and then back extracted into the alkaline solution (acceptor phase) inside the lumen of the hollow fiber. The fiber was held by a conventional 10 mu L LC syringe. The acceptor phase was sandwitched between the plunger and a small volume of the organic solvent (microcap). The acceptor solution was repeatedly moved in and out of the hollow fiber using a syringe pump. This movement provides a fresh acceptor phase to come in contact with the organic phase and thus enhancing extraction kinetics thereby leading to the improvement in enrichment of the analytes. The microcap separates the acceptor phase and the donor phase in addition to being partially responsible for mass transfer of the analytes from the donor solution to the acceptor solution. Under stirring, a fresh donor phase will enter through the open end of the fiber that will also contribute to the mass transfer. Various parameters affecting the extraction efficiency viz type of organic solvent, extraction time, stirring speed, effect of sodium chloride, and concentration of donor and acceptor phases were studied. RSD (3.9-5.6%), correlation coefficient (0.995-0.997), detection limit (2.0-51.2 ng/mL), enrichment factor (339-630), relative recovery (93.2-97.9%), and absolute recovery (33.9-63.0%) have also been investigated. The developed method was applied for the analysis of river water.
机译:描述了利用受体的自动移动和供体相技术进行的液-液-液微萃取,该技术使用一次性的即用型中空纤维在河水中萃取六种羟基芳族化合物。使用LC和254 nm紫外检测,进行分离和定量分析。将分析物从酸化的样品溶液(供体相)中提取到浸渍在中空纤维孔中的有机溶剂中,然后再提取到中空纤维管腔内的碱性溶液中(受体相)。用常规的10μLLC注射器固定纤维。受体相在柱塞和少量有机溶剂(微帽)之间被沙吸。使用注射泵将受体溶液反复移入和移出中空纤维。该运动提供了新鲜的受体相,使其与有机相接触,从而增强了萃取动力学,从而导致分析物富集度的提高。除了部分负责分析物从供体溶液到受体溶液的质量转移外,微帽还分离了受体相和供体相。在搅拌下,新鲜的供体相将从纤维的开口端进入,这也将有助于质量传递。研究了影响萃取效率的各种参数,即有机溶剂的类型,萃取时间,搅拌速度,氯化钠的作用以及供体和受体相的浓度。 RSD(3.9-5.6%),相关系数(0.995-0.997),检出限(2.0-51.2 ng / mL),富集因子(339-630),相对回收率(93.2-97.9%)和绝对回收率(33.9- 63.0%)也已被调查。将该方法用于河水分析。

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