Suppr超能文献

采用双(三甲基硅基)三氟乙酰胺进行纤维上衍生化的水中1,3-二氯-2-丙醇测定的固相微萃取方法。

Solid-phase micro-extraction procedure for the determination of 1,3-dichloro-2-propanol in water by on-fibre derivatisation with bis(trimethylsilyl)trifluoroacetamide.

作者信息

Carro Antonia María, González Paula, Fajar Noelia, Lorenzo Rosa Antonia, Cela Rafael

机构信息

Dpto. de Química Analítica, Nutrición y Bromatología, Facultad de Química, Instituto de Investigaciones y Análisis Alimentarios, Universidad de Santiago de Compostela, Avda. de las Ciencias s/n, 15782, Santiago de Compostela, Spain.

出版信息

Anal Bioanal Chem. 2009 Jun;394(3):893-901. doi: 10.1007/s00216-009-2769-x. Epub 2009 Apr 10.

Abstract

The headspace solid-phase micro-extraction technique with on-fibre derivatisation followed by gas chromatography-tandem mass spectrometry has been evaluated for the analysis of 1,3-dichloro-2-propanol in water. An asymmetric factorial design has been performed to study the influence of five experimental factors: extraction time and temperature, derivatisation time and temperature and pH. The best extraction performance is achieved in the headspace mode, with 5 mL stirred water samples (pH 4) containing 1.3 g of NaCl, equilibrated for 30 min at 25 degrees C, using divinylbenzene-carboxen-polydimethylsiloxane as the fibre coating. On-fibre derivatisation has been used for the first time with 50 microL of bis(trimethylsilyl)trifluoroacetamide at 25 degrees C during 15 min, leading to effective yields. The proposed method provides high sensitivity, good linearity and repeatability (relative standard deviation of 5.1% for 10 ng mL(-1) and n = 5). The limits of detection and quantification were 0.4 and 1.4 ng mL(-1), respectively. Analytical recoveries obtained for different water samples were approx. 100%.

摘要

已对顶空固相微萃取技术(采用纤维上衍生化,随后进行气相色谱 - 串联质谱分析)用于分析水中1,3 - 二氯 - 2 - 丙醇进行了评估。进行了非对称析因设计以研究五个实验因素的影响:萃取时间和温度、衍生化时间和温度以及pH值。在顶空模式下可实现最佳萃取性能,使用含有1.3 g氯化钠的5 mL搅拌水样(pH 4),在25℃下平衡30分钟,采用二乙烯基苯 - 碳分子筛 - 聚二甲基硅氧烷作为纤维涂层。首次在25℃下使用50 μL双(三甲基硅基)三氟乙酰胺进行15分钟的纤维上衍生化,获得了有效的产率。所提出的方法具有高灵敏度、良好的线性和重复性(对于10 ng mL⁻¹,n = 5时相对标准偏差为5.1%)。检测限和定量限分别为0.4和1.4 ng mL⁻¹。不同水样的分析回收率约为100%。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验