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J Chromatogr A


Title:Multidimensional gas chromatography using microfluidic switching and low thermal mass gas chromatography for the characterization of targeted volatile organic compounds
Author(s):Luong J; Gras R; Hawryluk M; Shellie RA; Cortes HJ;
Address:"Australian Centre for Research on Separation Science ACROSS, University of Tasmania, Private Bag 75, Hobart, Tasmania 7001, Australia"
Journal Title:J Chromatogr A
Year:2013
Volume:20130306
Issue:
Page Number:105 - 110
DOI: 10.1016/j.chroma.2013.02.084
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"Volatile organic compounds such as light hydrocarbons, dienes, and aromatic compounds are often encountered in the manufacturing and processing environments of chemical and petrochemical segments. These compounds need to be closely monitored for process optimization, plant maintenance and industrial hygiene purposes. A high throughput analytical approach has been successfully developed and implemented for the accurate measurement of fourteen commonly encountered analytes. The approach incorporates a recently introduced 5-port planar microfluidic device configured for use as a Deans switch for multidimensional gas chromatography. The use of multidimensional gas chromatography allows the elimination of potential chromatographic contaminants with a substantial enhancement of stationary phase selectivity via the use of columns with different separation mechanisms, and the back-flushing of heavier undesired hydrocarbons. A low thermal mass gas chromatographic module was employed in the second dimension of the two-dimensional gas chromatography system and was used to provide independent temperature control, and rapid heating and cooling to meet the high throughput requirements. By successfully combining these concepts, complete analysis of fourteen targeted components can be conducted in less than 120s. Repeatability of retention times for all compounds was found to be less than 0.05% (n=20). Repeatability of area counts at two levels, namely 10ppmv and 1000ppmv over a period of two days was found to be less than 3% (n=20). Apart from methane, which has a detection limit of 0.4ppmv, the rest of the compounds were found to have detection limits of less than 0.2ppmv. Compounds of interest were found to be linear over a range of 500ppbv-3000ppmv with correlation coefficients greater than 0.999"
Keywords:"Chromatography, Gas/*instrumentation/*methods High-Throughput Screening Assays/instrumentation/methods Limit of Detection Microfluidic Analytical Techniques/*instrumentation Reproducibility of Results Volatile Organic Compounds/*analysis/chemistry;"
Notes:"MedlineLuong, J Gras, R Hawryluk, M Shellie, R A Cortes, H J eng Research Support, Non-U.S. Gov't Netherlands 2013/03/26 J Chromatogr A. 2013 May 3; 1288:105-10. doi: 10.1016/j.chroma.2013.02.084. Epub 2013 Mar 6"

 
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