Simultaneous determination of triclocarban and triclosan in municipal biosolids by liquid chromatography tandem mass spectrometry

质谱法 废水 检出限 污水处理 污水污泥 串联质谱法 流出物 选择性反应监测
作者
Shi-Jye Chu,Chris D. Metcalfe
出处
期刊:Journal of Chromatography A [Elsevier]
卷期号:1164 (1-2): 212-218 被引量:187
标识
DOI:10.1016/j.chroma.2007.07.024
摘要

A sensitive and accurate method was developed for the simultaneous determination of triclosan and triclocarban in sludge and treated biosolids from municipal wastewater treatment plants (WWTPs). The methods involved extraction by pressurized liquid extraction (PLE), followed by sample clean-up on a Oasis HLB solid phase extraction (SPE) cartridge and analysis by liquid chromatography with electrospray ionization and tandem mass spectrometry (LC-ESI-MS/MS). Accurate quantification was achieved by isotope dilution using stable isotopes of triclosan and triclocarban as internal standards. Matrix effects (ME) in samples of spiked biosolids (n=5) were evaluated by a standard addition method, and these analyses indicated mean ME values of 79.7+/-6.7 and 100.5+/-8.4% for triclosan and triclocarban, respectively; indicating that the sample clean-up method effectively removed interferences. The mean recoveries from the spiked biosolids sample were 97.7+/-6.2 and 98.3+/-5 for triclosan and triclocarban, respectively, and the limits of detection (LOD) were 1.5 and 0.2 ng/g (d.w.) for triclosan and triclocarban, respectively. The method was applied to the analysis of triclosan and triclocarban in samples of activated sludge and treated biosolids collected from three WWTPs in Ontario, Canada. These preliminary results indicate that triclosan and triclocarban co-occur in municipal sludge and treated biosolids at concentrations ranging from 0.62 to 11.55 microg/g dry weight for triclosan, and from 2.17 to 5.97 microg/g dry weight for triclocarban.
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