Temperature dependence of ion mobility signals of halogenated compounds

被引:28
作者
Borsdorf, Helko [1 ]
Mayer, Thomas [1 ]
机构
[1] UFZ Helmholtz Ctr Environm Res, Dept Monitoring & Explorat Technol, D-04318 Leipzig, Germany
关键词
Ion mobility spectrometry; Chlorinated compounds; Dissociative charge transfer; Temperature dependence; Resolution; AB-INITIO; ELECTRON-ATTACHMENT; MOLECULE REACTIONS; SPECTROMETRY; CLUSTERS; PRESSURE; SPECTRA; CHROMATOGRAPHY; GROUNDWATER; ENERGETICS;
D O I
10.1016/j.talanta.2012.08.049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ion mobility spectrometry (IMS) as handheld and transportable sensor technique permits the sensitive detection of halogenated compounds with importance in environmental monitoring and process control. The negative ion mobility spectra mostly show one product ion peak which can be attributed to (H2O)(n)X- ions due to dissociative electron attachments. For minimizing memory effects and contaminations, modern ion mobility spectrometers work at elevated temperatures. In this paper, we investigated the influence of temperature on peak position, resolution and relative abundance of ions formed from halogenated substances. Elevated temperatures affect the peak position in different way. For fluorine- and chlorine-containing product ions, changes in hydration and clustering have a considerable influence on peak position, while these processes are of minor importance for bromineand iodine-containing product ions. In these cases, the drift time differences mainly result from differences in drift behavior due to differences in gas density, the mean free path of ions and different collision rates. The drift time shift with elevated temperatures provides an enhanced peak-to-peak resolution. Improved separation efficiency can therefore be established with increased temperatures for negative product ions of halogenated compounds. Furthermore, an enhanced sensitivity was found for all compounds with increasing temperatures. However, independent on the temperature, the order of sensitivity is mainly determined by the bonding state of halogen atoms within the molecules. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 23
页数:7
相关论文
共 27 条
[1]   SIMION ion optics simulations at atmospheric pressure [J].
Appelhans, AD ;
Dahl, DA .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2005, 244 (01) :1-14
[2]   Ab initio studies of O2- (H2O)n and O3- (H2O)n anionic molecular clusters, n≤12 [J].
Bork, N. ;
Kurten, T. ;
Enghoff, M. B. ;
Pedersen, J. O. P. ;
Mikkelsen, K. V. ;
Svensmark, H. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2011, 11 (14) :7133-7142
[3]   Rapid on-site determination of chlorobenzene in water samples using ion mobility spectrometry [J].
Borsdorf, H ;
Rämmler, A ;
Schulze, D ;
Boadu, KO ;
Feist, B ;
Weiss, H .
ANALYTICA CHIMICA ACTA, 2001, 440 (01) :63-70
[4]   Ion mobility spectrometry: Principles and applications [J].
Borsdorf, Helko ;
Eiceman, Gary A. .
APPLIED SPECTROSCOPY REVIEWS, 2006, 41 (04) :323-375
[5]   Recent Developments in Ion Mobility Spectrometry [J].
Borsdorf, Helko ;
Mayer, Thomas ;
Zarejousheghani, Mashaalah ;
Eiceman, Gary A. .
APPLIED SPECTROSCOPY REVIEWS, 2011, 46 (06) :472-521
[6]   Response of halogenated compounds in ion mobility spectrometry depending on their structural features [J].
Borsdorf, Helko ;
Mayer, Thomas .
TALANTA, 2011, 83 (03) :815-822
[7]   THEORETICAL-STUDIES OF O-2(-)-(H2O)N CLUSTERS [J].
CURTISS, LA ;
MELENDRES, CA ;
REED, AE ;
WEINHOLD, F .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1986, 7 (03) :294-305
[8]   Membrane-Extraction Ion Mobility Spectrometry for in Situ Detection of Chlorinated Hydrocarbons in Water [J].
Du, Yongzhai ;
Zhang, Wei ;
Whitten, William ;
Li, Haiyang ;
Watson, David B. ;
Xu, Jun .
ANALYTICAL CHEMISTRY, 2010, 82 (10) :4089-4096
[9]   Chemical class information in ion mobility spectra at low and elevated temperatures [J].
Eiceman, GA ;
Nazarov, EG ;
Rodriguez, JE .
ANALYTICA CHIMICA ACTA, 2001, 433 (01) :53-70
[10]   Predicting optimal resolving power for ambient pressure ion mobility spectrometry [J].
Kanu, Abu B. ;
Gribb, Molly M. ;
Hill, Herbert H., Jr. .
ANALYTICAL CHEMISTRY, 2008, 80 (17) :6610-6619