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在线-packed 固相微萃取-气相色谱-质谱法测定水样中的紫外线吸收剂和多环麝香化合物。

At-line microextraction by packed sorbent-gas chromatography-mass spectrometry for the determination of UV filter and polycyclic musk compounds in water samples.

机构信息

Helmholtz Centre for Environmental Research-UFZ, Department of Analytical Chemistry, Permoserstrasse 15, D-04318 Leipzig, Germany.

出版信息

J Chromatogr A. 2010 Apr 23;1217(17):2925-32. doi: 10.1016/j.chroma.2010.02.057. Epub 2010 Mar 3.

Abstract

An at-line analysis protocol is presented that allows the determination of four UV filters, two polycyclic musk compounds and caffeine in water at concentration level of ng L(-1). The fully automated method includes analytes enrichment by Microextraction by packed sorbent (MEPS) coupled directly to large volume injection-gas chromatography-mass spectrometry. Two common SPE phases, C8 and C18, were examined for their suitability to extract the target substances by MEPS. The analytes were extracted from small sample volumes of 800 microL with recoveries ranging from 46 to 114% for the C8-sorbent and 65-109% for the C18-sorbent. Limits of detection between 34 and 96 ng L(-1) enable the determination of the analytes at common environmental concentration levels. Both sorbents showed linear calibration curves for most of the analytes up to a concentration level of 20 ng mL(-1). Carryover was minimized by washing the sorbents 10 times with 100 microL methanol. After this thorough cleaning, the MEPS are re-used and up to 70 analyses can be performed with the same sorbent. The fully automated microextraction GC-MS protocol was evaluated for the influence of matrix substances typical for wastewater. Dilution of samples prior to MEPS is recommended when the polar caffeine is present at high concentration. Real water samples were analyzed by the MEPS-GC-MS method and compared to standard SPE.

摘要

现提出一种在线分析方案,可测定水中浓度为 ng L(-1) 的四种紫外线滤光剂、两种多环麝香化合物和咖啡因。该全自动方法包括通过直接与大体积进样-气相色谱-质谱联用的填充固相微萃取(MEPS)对分析物进行富集。研究了两种常见的 SPE 相(C8 和 C18),考察其通过 MEPS 提取目标物质的适用性。从 800 μL 的小样品体积中提取分析物,C8 吸附剂的回收率为 46%至 114%,C18 吸附剂的回收率为 65%至 109%。检测限在 34 至 96 ng L(-1) 之间,使这些分析物能够在常见的环境浓度水平下进行测定。两种吸附剂对大多数分析物的校准曲线在 20 ng mL(-1) 浓度水平下呈线性。通过用 100 μL 甲醇洗涤吸附剂 10 次,可将携带污染降至最低。在彻底清洗后,可重新使用 MEPS,每个吸附剂可进行多达 70 次分析。采用 MEPS-GC-MS 方法对废水典型基质物质的影响进行了评估。当极性咖啡因浓度较高时,建议在进行 MEPS 之前对样品进行稀释。实际水样通过 MEPS-GC-MS 方法进行分析,并与标准 SPE 进行了比较。

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