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用于气相色谱法测定水中卤乙酸的原位衍生化及中空纤维膜微萃取法

In situ derivatization and hollow fiber membrane microextraction for gas chromatographic determination of haloacetic acids in water.

作者信息

Varanusupakul Pakorn, Vora-Adisak Narongchai, Pulpoka Bancha

机构信息

Chromatography and Separation Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn University, Phayathai Road, Patumwan, Bangkok 10330, Thailand.

出版信息

Anal Chim Acta. 2007 Aug 13;598(1):82-6. doi: 10.1016/j.aca.2007.07.025. Epub 2007 Jul 14.

Abstract

An alternative method for gas chromatographic determination of haloacetic acids (HAAs) in water using direct derivatization followed by hollow fiber membrane liquid-phase microextraction (HF-LPME) has been developed. The method has improved the sample preparation step according to the conventional US EPA Method 552.2 by combining the derivatization and the extraction into one step prior to determination by gas chromatography electron captured detector (GC-ECD). The HAAs were derivatized with acidic methanol into their methyl esters and simultaneously extracted with supported liquid hollow fiber membrane in headspace mode. The derivatization was attempted directly in water sample without sample evaporation. The HF-LPME was performed using 1-octanol as the extracting solvent at 55 degrees C for 60 min with 20% Na2SO4. The linear calibration curves were observed for the concentrations ranging from 1 to 300 microg L(-1) with the correlation coefficients (R2) being greater than 0.99. The method detection limits of most analytes were below 1 microg L(-1) except DCAA and MCAA that were 2 and 18 microg L(-1), respectively. The recoveries from spiked concentration ranged from 97 to 109% with %R.S.D. less than 12%. The method was applied for determination of HAAs in drinking water and tap water samples. The method offers an easy one step high sample throughput sample preparation for gas chromatographic determination of haloacetic acids as well as other contaminants in water.

摘要

已开发出一种气相色谱法测定水中卤乙酸(HAAs)的替代方法,该方法采用直接衍生化,随后进行中空纤维膜液相微萃取(HF-LPME)。该方法根据美国环保局传统的方法552.2改进了样品制备步骤,通过在气相色谱电子捕获检测器(GC-ECD)测定之前将衍生化和萃取合并为一个步骤。卤乙酸用酸性甲醇衍生化为甲酯,同时在顶空模式下用支撑液膜中空纤维进行萃取。尝试直接在水样中进行衍生化,无需样品蒸发。HF-LPME使用1-辛醇作为萃取溶剂,在55℃下与20%的Na2SO4一起进行60分钟。浓度范围为1至300μg L(-1)时观察到线性校准曲线,相关系数(R2)大于0.99。除二氯乙酸(DCAA)和一氯乙酸(MCAA)的方法检测限分别为2和18μg L(-1)外,大多数分析物的方法检测限低于1μg L(-1)。加标浓度的回收率范围为97%至109%,相对标准偏差(%R.S.D.)小于12%。该方法用于测定饮用水和自来水样品中的卤乙酸。该方法为气相色谱法测定水中卤乙酸以及其他污染物提供了一种简单的一步高样品通量的样品制备方法。

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