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Journal of Chromatography A
Volume 1135, Issue 2, 1 December 2006, Pages 230-240
 
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doi:10.1016/j.chroma.2006.09.086    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Elsevier B.V. All rights reserved.

Rapid determination of complex mixtures by dual-column gas chromatography with a novel stationary phase combination and spectrometric detection

Gordon R. Lambertusa, Corresponding Author Contact Information, E-mail The Corresponding Author, Jeffrey A. Crankb, Megan E. McGuiganc, Shai Kendlera, d, Daniel W. Armstrongb and Richard D. Sacksa

aDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USA bDepartment of Chemistry, University of Texas at Arlington, Arlington, TX 76019, USA cDepartment of Atmospheric, Oceanic, and Space Science, University of Michigan, Ann Arbor, MI 48109, USA dIsreal Institute of Biological Research, Department of Physical Chemistry, Ness-Ziona 74100, Israel

Received 21 June 2006; 
revised 13 September 2006; 
accepted 15 September 2006. 
Available online 24 October 2006.

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Abstract

Fast GC separations of a broad range of analytes are demonstrated using a capillary column coated with a novel immobilized ionic liquid (IIL) stationary phase. Both completely cross-linked and partially cross-linked columns were evaluated, yielding not, vert, similar1600 and not, vert, similar2000 theoretical plates per meter, respectively. Enhanced separation is demonstrated using a dual-column ensemble comprised of an IIL column, a commercially coated Rtx-1 column, and a pneumatic valve connecting the inlet to the junction point between the two columns. Enhanced separation of 20 components, with two sets of co-eluting peaks is shown in not, vert, similar150 s, while sacrificing only a length of time equivalent to the sum of the stop flow pulses, or about 15.5 s. A novel application of a band trajectory model that shows band position as a function of analysis time as analytes move through the column ensemble is employed to determine pulse application times. The model predicts component retention times within a few seconds. Another method of selectivity enhancement of the IIL stationary phase-coated columns is demonstrated using a differential mobility spectrometer (DMS) that provides a second dimension separation based on ion mobility in a high-frequency electrical field. The DMS is able to separate all but one set of co-eluting components from the IIL column. The separation of 13 components found in the headspace above U.S. currency is demonstrated using the IIL column in a dual-column ensemble as well as with the DMS.

Keywords: Ionic liquids; Gas chromatography; Tunable selectivity; Differential mobility spectrometry; Modeling

Article Outline

1. Introduction
2. Experimental
2.1. Apparatus
2.2. Column design
2.3. DMS design
2.4. Materials
3. Results and discussion
3.1. Column efficiency
3.2. Isothermal separations
3.3. Stop-flow operation
3.4. Application
3.5. Spectrometric detection
4. Conclusions
Acknowledgements
References









Journal of Chromatography A
Volume 1135, Issue 2, 1 December 2006, Pages 230-240
 
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