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采用三相液相微萃取-毛细管电泳法测定分配系数并分析硝基酚。

Determination of partition coefficient and analysis of nitrophenols by three-phase liquid-phase microextraction coupled with capillary electrophoresis.

机构信息

Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, Skudai, Johor, Malaysia.

出版信息

J Sep Sci. 2010 Jul;33(14):2131-9. doi: 10.1002/jssc.201000172.

Abstract

A three-phase hollow fiber liquid-phase microextraction method coupled with CE was developed and used for the determination of partition coefficients and analysis of selected nitrophenols in water samples. The selected nitrophenols were extracted from 14 mL of aqueous solution (donor solution) with the pH adjusted to pH 3 into an organic phase (1-octanol) immobilized in the pores of the hollow fiber and finally backextracted into 40.0 microL of the acceptor phase (NaOH) at pH 12.0 located inside the lumen of the hollow fiber. The extractions were carried out under the following optimum conditions: donor solution, 0.05 M H(3)PO(4), pH 3.0; organic solvent, 1-octanol; acceptor solution, 40 microL of 0.1 M NaOH, pH 12.0; agitation rate, 1050 rpm; extraction time, 15 min. Under optimized conditions, the calibration curves for the analytes were linear in the range of 0.05-0.30 mg/L with r(2)>0.9900 and LODs were in the range of 0.01-0.04 mg/L with RSDs of 1.25-2.32%. Excellent enrichment factors of up to 398-folds were obtained. It was found that the partition coefficient (K(a/d)) values were high for 2-nitrophenol, 3-nitrophenol, 4-nitrophenol, 2,4-dinitrophenol and 2,6-dinitrophenol and that the individual partition coefficients (K(org/d) and K(a/org)) promoted efficient simultaneous extraction from the donor through the organic phase and further into the acceptor phase. The developed method was successfully applied for the analysis of water samples.

摘要

建立了一种三相中空纤维液相微萃取(LPME)方法,并与 CE 结合,用于测定水中分配系数和分析选定的硝基酚类物质。将选定的硝基酚类物质从 14 mL 水(供体溶液)中提取,pH 调至 3,进入固定在中空纤维孔中的有机相(1-辛醇),最后在 pH 12.0 的接受相(NaOH)中反萃取 40.0 µL,位于中空纤维的内腔中。在以下最佳条件下进行萃取:供体溶液,0.05 M H(3)PO(4),pH 3.0;有机溶剂,1-辛醇;接受溶液,40 µL 0.1 M NaOH,pH 12.0;搅拌速度,1050 rpm;萃取时间,15 min。在优化条件下,分析物的校准曲线在 0.05-0.30 mg/L 范围内呈线性,r(2)>0.9900,LOD 范围在 0.01-0.04 mg/L 之间,RSD 为 1.25-2.32%。获得了高达 398 倍的优异富集因子。发现 2-硝基酚、3-硝基酚、4-硝基酚、2,4-二硝基酚和 2,6-二硝基酚的分配系数(K(a/d))值较高,且各个分配系数(K(org/d)和 K(a/org))促进了从供体通过有机相到接受相的高效同时萃取。所建立的方法成功地应用于水样分析。

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