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采用微波辅助萃取-气相色谱-质谱法(电子轰击和化学电离)测定沉积物中的有机磷阻燃剂。

Determination of organophosphate flame retardants in sediments by microwave-assisted extraction and gas chromatography-mass spectrometry with electron impact and chemical ionization.

机构信息

Department of Chemistry, National Central University, Chung-Li 320, Taiwan.

出版信息

Anal Bioanal Chem. 2009 Dec;395(7):2325-34. doi: 10.1007/s00216-009-3139-4. Epub 2009 Sep 27.

Abstract

An efficient microwave-assisted extraction (MAE) procedure coupled to gas chromatography-mass spectrometry (GC-MS) with electron impact (EI) and chemical ionization (CI) has been developed to determine five organophosphate flame retardants (OPFRs) in marine and river sediments. The effects of various operating parameters on the quantitative extraction of the OPFRs through MAE were systematically investigated. Selected OPFRs were extracted from the sediments through MAE using 40 mL of acetone at 120 degrees C for 20 min. The limits of quantitation ranged from 0.1 to 0.4 ng/g (dry weight) in 2 g of the sediment samples. Moreover, as the chlorinated alkyl phosphates present no molecular ions in EI, GC-MS with furan-CI (furan-CI) was applied to confirm their determination in complex environmental samples. The recoveries of the selected OPFRs in spiked sediment samples ranged from 62% to 106% (relative standard derivation, 1-11%). The total concentrations of the selected OPFR residues in marine and river sediments ranged from 1.0 to 12.6 ng/g.

摘要

建立了一种高效的微波辅助萃取(MAE)方法,并结合气相色谱-质谱(GC-MS)联用技术,其中包括电子轰击(EI)和化学电离(CI),用于测定海洋和河流沉积物中的五种有机磷酸酯阻燃剂(OPFRs)。系统研究了各种操作参数对 MAE 定量萃取 OPFRs 的影响。通过 MAE 用 40 毫升丙酮在 120°C 下萃取 20 分钟,从沉积物中提取选定的 OPFRs。在 2 克沉积物样品中,定量下限范围为 0.1 至 0.4 纳克/克(干重)。此外,由于 EI 中不存在氯化烷基磷酸酯的分子离子,因此应用呋喃-CI(furan-CI)GC-MS 来确认在复杂环境样品中的测定。在加标沉积物样品中,选定的 OPFRs 的回收率范围为 62%至 106%(相对标准偏差为 1-11%)。海洋和河流沉积物中选定的 OPFR 残留的总浓度范围为 1.0 至 12.6 纳克/克。

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