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通过大气压化学电离质谱法对气流中的正构烷烃进行快速在线分析。

Rapid online analysis of n-alkanes in gaseous streams via APCI mass spectrometry.

作者信息

Wentrup Jonas, Bösing Ingmar, Dülcks Thomas, Thöming Jorg

机构信息

Faculty of Production Engineering, Chemical Process Engineering, University of Bremen, Leobener Strasse 6, 28359, Bremen, Germany.

Center for Environmental Research and Sustainable Technology, University of Bremen, Postbox 330 440, 28334, Bremen, Germany.

出版信息

Anal Bioanal Chem. 2024 Mar;416(8):1843-1855. doi: 10.1007/s00216-024-05182-3. Epub 2024 Feb 15.

Abstract

Online monitoring of dynamic chemical processes involving a wide volatility range of hydrocarbon species is challenging due to long chromatographic measurement times. Mass spectrometry (MS) overcomes chromatographic delays. However, the analysis of n-alkane mixtures by MS is difficult because many fragment ions are formed, which leads to overlapping signals of the homologous series. Atmospheric pressure chemical ionization (APCI) is suitable for the analysis of saturated hydrocarbons and is the subject of current research. Still, although APCI is a "soft ionization" technique, fragmentation is typically inevitable. Moreover, it is usually applied for liquid samples, while an application for online gas-phase monitoring is widely unexplored. Here, we present an automated APCI-MS method for an online gas-phase analysis of volatile and semi-volatile n-alkanes. Mass spectra for n-heptane and n-decane reveal [M-H], [M-3H] and [M-3H+HO] as abundant ions. While [M-H] and [M-3H] show an excessive fragmentation pattern to smaller CH and CH cations, [M-3H+HO] is the only relevant signal within the CHO ion group, i.e., no chain cleavage is observed. This makes [M-3H+HO] an analyte-specific ion that is suitable for the quantification of n-alkane mixtures. A calibration confirms the linearity of C and C signals up to concentrations of ~1000-1500 ppm. Moreover, validated concentration profiles are measured for a binary C/C mixture and a five-alkane C/C/C/C/C mixture. Compared to the 40-min sampling interval of the reference gas chromatograph, MS sampling is performed within 5 min and allows dynamic changes to be monitored.

摘要

由于色谱测量时间较长,对涉及多种挥发性烃类的动态化学过程进行在线监测具有挑战性。质谱(MS)克服了色谱延迟问题。然而,用质谱分析正构烷烃混合物很困难,因为会形成许多碎片离子,导致同系物系列信号重叠。大气压化学电离(APCI)适用于饱和烃的分析,是当前研究的主题。尽管APCI是一种“软电离”技术,但碎片化通常是不可避免的。此外,它通常用于液体样品,而在线气相监测的应用尚未得到广泛探索。在此,我们提出了一种用于挥发性和半挥发性正构烷烃在线气相分析的自动化APCI-MS方法。正庚烷和正癸烷的质谱显示,[M-H]、[M-3H]和[M-3H+HO]为丰富离子。虽然[M-H]和[M-3H]呈现出过度碎片化形成较小的CH和CH阳离子的模式,但[M-3H+HO]是CHO离子组内唯一相关信号,即未观察到链断裂。这使得[M-3H+HO]成为适合定量正构烷烃混合物的分析物特异性离子。校准证实了C和C信号在浓度高达~1000-1500 ppm时的线性关系。此外,还测量了二元C/C混合物和五元烷烃C/C/C/C/C混合物的有效浓度分布。与参考气相色谱仪40分钟的采样间隔相比,质谱采样在5分钟内完成,并能监测动态变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55e/10902047/6ff8f62fec46/216_2024_5182_Fig1_HTML.jpg

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