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[酮类有机化合物的放电离子迁移谱法]

[Discharge ion mobility spectrometry of ketonic organic compounds].

作者信息

Huang Guo-dong, Han Hai-yan, Jia Xian-de, Jin Shun-ping, Li Jian-quan, Wang Hong-mei, Tang Xiao-shuan, Jiang Hai-he, Chu Yan-nan, Zhou Shi-kang

机构信息

Laboratory of Environmental Spectroscopy, Anhui Institute of Optics and Fine Mechanics, Key Laboratory of Environmental Optics and Technology, Chinese Academy of Sciences, Hefei 230031, China.

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2007 May;27(5):833-6.

Abstract

Ion mobility spectrometry (IMS) is a sensitive technique for fast on-line monitoring trace volatile organic compounds based upon the mobilities of gas phase ions at ambient pressure in weak electric field. In the present work, protonated water reactant ions were successfully prepared, and eight ketones were studied on a homemade high-resolution IMS apparatus using a discharge ionization source. The reduced mobility values of all ions were derived from the observed ion mobility spectra. The experimentally determined reduced mobilities for acetone, 2-butone, 1-methyl-2-pyrrolidinone acetophenone, cyclohexanone and product ions were compared with the previously reported values in the Ni-IMS, indicating that they are in good agreement. The reduced mobilities of methyl isopropyl ketone, 4-methyl-2-pentanone and cyclopentanone ions were given for the first time. The ionization process for organic compounds in the authors' discharge ion mobility spectrometer is suggested to be similar to Ni-IMS system, i.e., the proton transfer reactions produce protonated ketone ions. In addition, a linear correlation was found between the reduced mobilities of the ketone ions and their molecular masses. Qualitative measurements show that the limit of detection is in the ng x L(-1) order of magnitude in the authors' discharge ion mobility spectrometer.

摘要

离子迁移谱(IMS)是一种基于弱电场中常压下气相离子迁移率的快速在线监测痕量挥发性有机化合物的灵敏技术。在本工作中,成功制备了质子化水反应物离子,并在一台使用放电电离源的自制高分辨率IMS仪器上对8种酮类进行了研究。所有离子的折合迁移率值均从观测到的离子迁移谱中得出。将实验测定的丙酮、2-丁酮、1-甲基-2-吡咯烷酮、苯乙酮、环己酮及其产物离子的折合迁移率与镍离子迁移谱(Ni-IMS)中先前报道的值进行了比较,结果表明二者吻合良好。首次给出了甲基异丙基酮、4-甲基-2-戊酮和环戊酮离子的折合迁移率。作者认为,其放电离子迁移谱仪中有机化合物的电离过程与Ni-IMS系统相似,即质子转移反应产生质子化酮离子。此外,还发现酮离子的折合迁移率与其分子量之间存在线性相关性。定性测量表明,作者的放电离子迁移谱仪的检测限在纳克×升⁻¹数量级。

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