Quantitative determination of triclocarban in wastewater effluent by stir bar sorptive extraction and liquid desorption–liquid chromatography–tandem mass spectrometry

摘要

Triclocarban is an antimicrobial and antibacterial agent found in personal care products and subsequently is a prevalent wastewater contaminant.Aquantitative method was developed for the analysis of triclocarban in wastewater effluents using stir bar sorptive extraction–liquid desorption (SBSE–LD) followed by liquid chromatography–tandem mass spectrometry (LC–MS/MS) by means of an electrospray interface. A stir bar coated with polydimethylsiloxane (PDMS) is placed within a vial containing wastewater effluent and is stirred for an hour at room temperature. The PDMS stir bar is then placed in a LC vial containing methanol and is desorbed in a sonicator bath. The methanol is evaporated to dryness and reconstituted in 75% methanol. Spike and recovery experiments in groundwater that did not contain native concentrations of triclocarban were performed at 0.5g/L and were 93±8%. Recoveries in wastewater effluent that were corrected for the background levels of triclocarban were 92±2% and 96±5%, respectively, when spiked with 0.5 and 5g/L of triclocarban. The precision of the method as indicated by the relative standard error was 2%. The limit of quantitation was 10 ng/L. The SBSE–LD–LC/MS/MS method was applied to wastewater effluent samples collected from northeast Ohio. Triclocarban was quantitated in all five effluent samples, and its concentration ranged from 50 to 330 ng/L. The described method demonstrates a simple, green, low-sample volume, yet, sensitive method to measure triclocarban in aqueous matrices.