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首页> 外文期刊>Analytica chimica acta >Solid phase microextraction procedure for the determination of alkylphenols in water by on-fiber derivatization with N-tcrt-butyl-dimethylsilyl-N-methyltrifluoroacetamide
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Solid phase microextraction procedure for the determination of alkylphenols in water by on-fiber derivatization with N-tcrt-butyl-dimethylsilyl-N-methyltrifluoroacetamide

机译:N-叔丁基丁基二甲基甲硅烷基-N-甲基三氟乙酰胺的纤维衍生化固相微萃取法测定水中的烷基酚

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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 2mL was placed in a 4mL PTFE-capped glass vial. Headspace extraction of APs in water was then performed under 65 °C for 30min with 800 rpm magnetic stirring and the addition of 5% of sodium chloride. In the second step, the SPME fiber was placed in another 4mL 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 ngL~(-1). Compared with other techniques, the study described here provided a simple, fast and reliable method for the analysis of APs in water.
机译:对纤维上衍生化的固相微萃取(SPME)技术进行了评估,以分析烷基酚(AP),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)在水中。使用85μm聚丙烯酸酯(PA)纤维,并建立了两步的样品制备程序。第一步,将2mL的水样品放入4mL PTFE封盖的玻璃小瓶中。然后在800 rpm磁力搅拌和添加5%的氯化钠的情况下,在65°C下进行30分钟的顶空萃取,在水中进行。在第二步中,将SPME纤维放入另一个4mL小瓶中,该小瓶中包含100μLN-叔丁基-二甲基甲硅烷基-N-甲基三氟乙酰胺(MTBSTFA)和1%叔丁基-二甲基氯硅烷(TBDMCS)。在45°C下进行MTBSTFA的顶空萃取和用AP进行纤维衍生化10分钟。气相色谱/质谱(GC / MS)用于分析纤维上形成的衍生物。还研究了吸附时间曲线。使用加标水样品(包括洗涤剂水,氯化自来水和湖水)评估了用于分析所有AP的精度,准确性和方法检测限(MDL)。相对标准偏差均小于10%,准确度为100±15%。使用2 mL水样品,MDL范围为1.58-3.85 ngL〜(-1)。与其他技术相比,此处描述的研究提供了一种简单,快速且可靠的方法来分析水中的AP。

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