Electromembrane extraction and HPLC analysis of haloacetic acids and aromatic acetic acids in wastewater

被引:52
作者
Alhooshani, Khalid [1 ]
Basheer, Chanbasha [1 ]
Kaur, Jagjit [2 ]
Gjelstad, Astrid [3 ]
Rasmussen, Knut E. [3 ]
Pedersen-Bjergaard, Stig [3 ]
Lee, Hian Kee [2 ]
机构
[1] King Fahd Univ Petr & Minerals, Dept Chem, KFUPM, Dhahran 31261, Saudi Arabia
[2] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[3] Univ Oslo, Sch Pharm, N-0316 Oslo, Norway
关键词
Microextraction; Electromembrane extraction; Disinfection by-products; Polar analytes; Environnemental analysis; IN-SITU DERIVATIZATION; GAS-CHROMATOGRAPHIC DETERMINATION; LIQUID-CHROMATOGRAPHY; PHASE MICROEXTRACTION; MASS-SPECTROMETRY; DRINKING-WATER; MEMBRANE MICROEXTRACTION; UV DETECTION; PHENOLS;
D O I
10.1016/j.talanta.2011.08.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
For the first time, haloacetic acids and aromatic acetic acids were extracted from wastewater samples using electromembrane extraction (EME). A thin layer of toluene immobilized on the walls of a polypropylene membrane envelope served as an artificial supported liquid membrane (SLM). The haloacetic acids (HAAs) (chloroacetic acid, dichloroacetic acid, and trifluoroacetic acid) and aromatic acetic acids (phenylacetic acid and p-hydroxyphenylacetic acid) were extracted through the SLM and into an alkalized aqueous buffer solution. The buffer solution was located inside the membrane envelope. The electrical potential difference sustained over the membrane acted as the driving force for the transport of haloacetic acids into the membrane by electrokinetic migration. After extraction, the extracts were analyzed by high-performance liquid chromatography-ultraviolet detection. The detection limits were between 0.072 and 40.3 ng L-1. The calibration plot linearity was in the range of 5 and 200 mu g L-1 while the correlation coefficients for the analytes ranged from 0.9932 to 0.9967. Relative recoveries were in the range of 87-106%. The extraction efficiency was found to be comparable to that of solid-phase extraction. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
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