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采用N-叔丁基二甲基硅基-N-甲基三氟乙酰胺进行纤维上衍生化的水相中烷基酚固相微萃取测定方法。

Solid phase microextraction procedure for the determination of alkylphenols in water by on-fiber derivatization with N-tert-butyl-dimethylsilyl-N-methyltrifluoroacetamide.

作者信息

Pan Yi-Ping, Tsai Shih-Wei

机构信息

Institute of Environmental Health, College of Public Health, National Taiwan University, No. 17, Xuzhou Road, Taipei 100, Taiwan.

出版信息

Anal Chim Acta. 2008 Aug 29;624(2):247-52. doi: 10.1016/j.aca.2008.06.039. Epub 2008 Jul 1.

Abstract

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 microm 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 degrees 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 microL 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 degrees 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.

摘要

采用带纤维上衍生化的固相微萃取(SPME)技术对水中的烷基酚(APs)进行分析,其中包括4-叔辛基酚(4-t-OP)、工业壬基酚异构体(t-NPs)和4-壬基酚(4-NP)。使用85微米的聚丙烯酸酯(PA)纤维,并建立了两步样品制备程序。第一步,将2毫升水样置于一个4毫升带聚四氟乙烯盖的玻璃小瓶中。然后在65℃下,以800转/分钟的磁力搅拌并加入5%的氯化钠,对水中的APs进行顶空萃取30分钟。第二步,将SPME纤维置于另一个4毫升的小瓶中,该小瓶中含有100微升含1%叔丁基二甲基氯硅烷(TBDMCS)的N-叔丁基二甲基硅基-N-甲基三氟乙酰胺(MTBSTFA)。在45℃下进行MTBSTFA的顶空萃取以及APs与纤维上的衍生化反应10分钟。采用气相色谱/质谱联用(GC/MS)对纤维上形成的衍生物进行分析。还研究了吸附时间曲线。通过向洗涤剂水、加氯自来水和湖水等加标水样中添加目标物,评估了所有APs分析的精密度、准确度和方法检出限(MDLs)。相对标准偏差均小于10%,准确度为100±15%。对于2毫升水样,MDLs在1.58 - 3.85纳克/升范围内。与其他技术相比,本文所述研究为水中APs的分析提供了一种简单、快速且可靠的方法。

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