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首页> 外文期刊>Journal of separation science. >Simultaneous dispersive liquid-liquid microextraction based on a low-density solvent and derivatization followed by gas chromatography for the simultaneous determination of chloroanisoles and the precursor 2,4,6-trichlorophenol in water samples
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Simultaneous dispersive liquid-liquid microextraction based on a low-density solvent and derivatization followed by gas chromatography for the simultaneous determination of chloroanisoles and the precursor 2,4,6-trichlorophenol in water samples

机译:基于低密度溶剂和衍生化的同时分散液-液微萃取,然后进行气相色谱法同时测定水中的氯苯甲醚和前体2,4,6-三氯苯酚

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摘要

Chloroanisoles, particularly 2,4,6-trichloroanisole, are commonly identified as major taste and odor compounds in water. In the present study, a simple and efficient method was established for the simultaneous determination of chloroanisoles and the precursor 2,4,6-trichlorophenol in water by using low-density-solvent-based simultaneous dispersive liquid-liquid microextraction and derivatization followed by gas chromatography with electron capture detection. 2,4-Dichloroanisole, 2,6-dichloroanisole, 2,4,6-trichloroanisole, 2,3,4-trichloroanisole, and 2,3,6-trichloroanisole were the chloroanisoles evaluated. Several important parameters of the extraction-derivatization procedures, including the types and volumes of extraction solvent and disperser solvent, concentrations of derivatization agent and base, salt addition, extraction-derivatization time, and temperature were optimized. Under the optimized conditions (80 mu L of isooctane as extraction solvent, 500 mu L of methanol as disperser solvent, 60 mu L of acetic anhydride as derivatization agent, 0.75% of Na2CO3 addition w/v, extraction-derivatization temperature of 25 degrees C, without salt addition), a good linearity of the calibration curve was observed by the square of correlation coefficients (R-2) ranging from 0.9936 to 0.9992. Repeatability and reproducibility of the method were < 4.5% and < 7.3%, respectively. Recovery rates ranged from 85.2 to 101.4%, and limits of detection ranged from 3.0 to 8.7 ng/L. The proposed method was applied successfully for the determination of chloroanisoles and 2,4,6-trichlorophenol in water samples.
机译:氯苯甲醚,特别是2,4,6-三氯苯甲醚,通常被认为是水中的主要味道和气味化合物。本研究建立了一种简单有效的方法,同时使用低密度溶剂基同时分散液-液微萃取和衍生化方法同时测定水中的氯苯甲醚和前体2,4,6-三氯苯酚电子捕获检测色谱。将2,4-二氯茴香醚,2,6-二氯茴香醚,2,4,6-三氯茴香醚,2,3,4-三氯茴香醚和2,3,6-三氯茴香醚进行了评价。优化了萃取-衍生化程序的几个重要参数,包括萃取溶剂和分散剂的类型和体积,衍生化剂和碱的浓度,盐的添加,萃取-衍生化的时间和温度。在优化的条件下(以异辛烷为提取溶剂80μL,以甲醇为分散剂500μL,以乙酸酐为衍生剂60μL,以w / v添加0.75%的Na2CO3,提取衍生化温度为25摄氏度(不添加盐),校正系数的线性良好,相关系数的平方(R-2)在0.9936至0.9992之间。该方法的重复性和重现性分别为<4.5%和<7.3%。回收率范围为85.2至101.4%,检测极限范围为3.0至8.7 ng / L。该方法成功用于水样中氯苯甲醚和2,4,6-三氯苯酚的测定。

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