Solid phase microextraction procedure for the determination of alkylphenols in water by on-fiber derivatization with N

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• 作者：Yi-Ping Pan ; Shih-Wei Tsai
• 关键词：Solid phase microextraction ; N-tert-butyl-dimethylsilyl-N-methyltrifluoroacetamide ; Alkylphenols ; Gas chromatography
• 刊名：Analytica Chimica Acta
• 出版年：2008
• 出版时间：29 August 2008
• 年：2008
• 卷：624
• 期：2
• 页码：247-252
• 全文大小：340 K

文摘

The solid phase microextraction (SPME) technique with on-fiber derivatization was evaluated for the analysis of alkylphenols (APs), including 4-tert-octylphenol (4-t-OP), technical nonylphenol isomers (t-NPs) and 4-nonylphenol (4-NP), in water. The 85 μm polyacrylate (PA) fiber was used and a two-step sample preparation procedure was established. In the first step, water sample of 2 mL was placed in a 4 mL PTFE-capped glass vial. Headspace extraction of APs in water was then performed under 65 °C for 30 min with 800 rpm magnetic stirring and the addition of 5 % of sodium chloride. In the second step, the SPME fiber was placed in another 4 mL vial, which contained 100 μL of N-tert-butyl-dimethylsilyl-N-methyltrifluoroacetamide (MTBSTFA) with 1 % tert-butyl-dimethylchlorosilane (TBDMCS). Headspace extraction of MTBSTFA and on-fiber derivatization with APs were performed at 45 °C for 10 min. Gas chromatography/mass spectrometry (GC/MS) was used for the analysis of derivatives formed on-fiber. The adsorption-time profiles were also examined. The precision, accuracy and method detection limits (MDLs) for the analysis of all the APs were evaluated with spiked water samples, including detergent water, chlorinated tap water, and lake water. The relative standard deviations were all less than 10 % and the accuracies were 100 ± 15 % . With 2 mL of water sample, MDLs were in the range of 1.58–3.85 ng L⁻¹. Compared with other techniques, the study described here provided a simple, fast and reliable method for the analysis of APs in water.