Suppr超能文献

[大气颗粒物滤膜上极性有机物在线衍生化装置的设计与应用]

[Design and application of online derivatization device for polar organics on atmospheric particulate filter].

作者信息

Zhang Han, Liao Xu, Wei Lai, Zhang Zixing, Ren Hongyun, Zhang Xian

机构信息

Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 China.

出版信息

Se Pu. 2022 Jan;40(1):100-106. doi: 10.3724/SP.J.1123.2021.03009.

Abstract

An online derivatization device for the analysis of polar organic compounds by gas chromatography-mass spectrometry (GC-MS) is designed. The derivatization reaction occurs in the hot GC injection port, and this is also known as injection port derivatization (IPD). IPD is usually performed in two ways: 1) direct IPD and 2) ion-pair extraction, followed by IPD. In both cases, the derivatization reagent reacts in liquid form. However, a method for online derivatization using gaseous derivatization reagents is provided. A special needle is designed and placed on the carrier gas transfer line to the injection port. The carrier gas is introduced into a glass bottle containing the derivative reagent (-methyl--(trimethylsilyl)trifluoroacetamide, MSTFA), and then, the gaseous derivative reagent in the headspace is pressed out and introduced into the injection port of the GC instrument at a constant speed. The filter to be analyzed is placed directly in the liner, and the polar organic compounds on the filter react with gaseous MSTFA at 310 ℃ for 10 min in the injection port. During derivatization, the column oven is maintained at room temperature, and all the derivatives stay on the column head. When the reaction is complete, the MSTFA supply is ceased. The oven temperature is programmed, and the solvent delay is set until the excessive MSTFA is removed. The derivatives are allowed to pass through the column and analyzed by the MS detector. To prevent a large number of derivative reagents from entering the column, the injection port is set in split mode with a split ratio of 5∶1. Variables such as the injection-port temperature and derivatization time are investigated. The GC-MS responses of the ten silylated derivatives increase with increasing injection-port temperature (290-310 ℃), indicating that high temperatures can enhance the silylation efficiency. The derivatization times were also investigated. The GC-MS responses increased with an increase in the reaction time from 0 to 10 min, while higher temperatures or longer reaction times lead to the loss of some derivatives. The reproducibility of the derivatization reaction was 0.27% to 7.28%, and the linear correlation coefficient was 0.976-0.996. This device can be used for the online silylation of most polar organic compounds such as organic acids, alcohols, and phenols. The advantage of this device over offline derivatization is that the derivatization reagent and derivatives are protected by helium, which eliminates the risk of decomposition caused by moisture in the air, and the high temperature assists the reaction. The analytes were directly desorbed on the filter and derived online, and the sample quantity required was only 1/200 of that in the traditional solvent extraction method. Meanwhile, only the gaseous part of the headspace in the derivative reagent bottle was used, and the amount of derivative reagent was greatly reduced. Additionally, the operation is simple and solvent free, the entire analytical procedure was executed in a "green" manner. A PM2.5 filter was analyzed, and 26 different polar compounds were successfully derived, including monoacids, binary acids, aromatic acids, and alcohols, covering most of the common target polar compounds in atmospheric chemical analysis. Polyols such as glucose and sorbose that bear 5-6 hydroxyl groups and have large steric hindrance were also successfully derived. This device is expected to be an efficient and convenient analytical tool for tracing the sources of organic matter in atmospheric particles such as soil dust, biomass combustion, cooking oil smoke, and automobile exhaust, or for investigating atmospheric photochemical reactions. This gas-phase derivatization provides new insights for the development of chromatographic analysis methods for polar compounds. This device is simple and modular, and it has a wide range of applications; it is suitable for different brands of gas chromatographs and has great prospects for commercialization.

摘要

设计了一种用于气相色谱 - 质谱联用(GC - MS)分析极性有机化合物的在线衍生化装置。衍生化反应在热的GC进样口中发生,这也被称为进样口衍生化(IPD)。IPD通常以两种方式进行:1)直接IPD和2)离子对萃取后再进行IPD。在这两种情况下,衍生化试剂均以液态形式反应。然而,提供了一种使用气态衍生化试剂进行在线衍生化的方法。设计了一种特殊的针,并将其放置在通向进样口的载气传输线上。将载气引入装有衍生化试剂(-甲基--(三甲基硅基)三氟乙酰胺,MSTFA)的玻璃瓶中,然后将顶空中的气态衍生化试剂以恒定速度压出并引入GC仪器的进样口。待分析的滤膜直接放置在衬管中,滤膜上的极性有机化合物在进样口中于310℃与气态MSTFA反应10分钟。衍生化过程中,柱温箱保持在室温,所有衍生物都保留在柱头。反应完成后,停止供应MSTFA。对柱温进行程序升温,并设置溶剂延迟时间直至过量的MSTFA被去除。使衍生物通过色谱柱并由MS检测器进行分析。为防止大量衍生化试剂进入色谱柱,进样口设置为分流模式,分流比为5∶1。研究了诸如进样口温度和衍生化时间等变量。十种硅烷化衍生物的GC - MS响应随着进样口温度(290 - 310℃)的升高而增加,表明高温可提高硅烷化效率。还研究了衍生化时间。GC - MS响应随着反应时间从0增加到10分钟而增加,而更高的温度或更长的反应时间会导致一些衍生物损失。衍生化反应的重现性为0.27%至7.28%,线性相关系数为0.976 - 0.996。该装置可用于大多数极性有机化合物如有机酸、醇和酚的在线硅烷化。该装置相对于离线衍生化的优势在于,衍生化试剂和衍生物受到氦气保护,消除了因空气中水分导致分解的风险,且高温有助于反应。分析物直接在滤膜上解吸并在线衍生化,所需样品量仅为传统溶剂萃取法的1/200。同时,仅使用了衍生化试剂瓶顶空中的气态部分,大大减少了衍生化试剂的用量。此外,操作简单且无溶剂,整个分析过程以“绿色”方式进行。对一个PM2.5滤膜进行了分析,成功衍生出26种不同的极性化合物,包括一元酸、二元酸、芳香酸和醇,涵盖了大气化学分析中大多数常见的目标极性化合物。带有5 - 6个羟基且空间位阻较大的多元醇如葡萄糖和山梨糖也成功进行了衍生化。该装置有望成为一种高效便捷的分析工具,用于追踪大气颗粒物中土壤扬尘、生物质燃烧、食用油烟雾和汽车尾气等有机物的来源,或用于研究大气光化学反应。这种气相衍生化为极性化合物色谱分析方法的发展提供了新的思路。该装置简单且模块化,具有广泛的应用;适用于不同品牌的气相色谱仪,具有很大的商业化前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56cb/9404233/4f35a29aeed1/cjc-40-01-100-img_1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验