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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Methyl chloroacetate as an extraction solvent for coupling liquid–liquid semimicroextraction with micellar electrokinetic chromatography through on-capillary decomposition for the separation of neutral compounds with concentration enhancement
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Methyl chloroacetate as an extraction solvent for coupling liquid–liquid semimicroextraction with micellar electrokinetic chromatography through on-capillary decomposition for the separation of neutral compounds with concentration enhancement

机译:氯乙酸甲酯作为萃取溶剂,通过毛细管内分解,将液-液半微萃取与胶束电动色谱耦合,用于分离中性化合物并提高浓度

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This paper reports the use of methyl chloroacetate (MCA) as an extraction solvent for coupling liquid–liquid semimicroextraction (LLsME) with micellar electrokinetic chromatography (MEKC) through on-capillary decomposition for the separation of neutral compounds with concentration enhancement. Alkylphenones of C8, C10 and C11 were chosen as modeling compounds. Aqueous samples of the alkylphenones were extracted by LLsME into methyl chloroacetate. The organic phase, after being separated from the aqueous phase, was directly subjected to separation by MEKC. The detection limits (S/N ≥ 3) were 0.05, 0.05 and 0.1 mg/L for butyrophenone, valerophenone and acetophenone in water, respectively, and the concentration factors of the extraction were in a range of 63 to 151-fold in terms of peak area for the three alkylphenones. Linearity and reproducibility of the method were also evaluated. Extraction and separation of a wastewater sample from a dye factory were included to demonstrate application potential of the method developed. The method developed has no requirement on any special experimental apparatuses other than a basic CE setup and is time saving and easy to operate. Therefore, it would be readily acceptable for routine analysis, especially for environmental water samples.
机译:本文报道了氯乙酸甲酯(MCA)作为萃取溶剂的应用,该方法通过毛细管内分解将液-液半微萃取(LLsME)与胶束电动色谱(MEKC)偶联,以提高浓度,分离中性化合物。选择C8,C10和C11的烷基苯酮作为建模化合物。通过LLsME将烷基苯酮的水样品萃取到氯乙酸甲酯中。与水相分离后的有机相通过MEKC直接分离。水中丁酮,戊戊酮和苯乙酮的检出限(S / N≥3)分别为0.05、0.05和0.1 mg / L,而提取物的浓缩系数在63到151倍之间三个烷基苯酮的峰面积。还评估了该方法的线性和重现性。包括从染料厂中提取和分离废水样品,以证明所开发方法的应用潜力。开发的方法除了基本的CE设置外,对任何特殊的实验设备都没有要求,并且省时且易于操作。因此,对于常规分析,尤其是环境水样,这将是容易接受的。

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