Thermal desorption comprehensive two-dimensional gas chromatography coupled to time of flight mass spectrometry for vapour phase mainstream tobacco smoke analysis
Autor: | Jean-François Focant, Benjamin Savareear, Chris J. Wright, Michal Brokl |
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Rok vydání: | 2017 |
Předmět: |
Sorbent
Polymers Analytical chemistry Tenax Thermal desorption 010501 environmental sciences Mass spectrometry 01 natural sciences Biochemistry Chemistry Techniques Analytical Gas Chromatography-Mass Spectrometry Analytical Chemistry Desorption Smoke Tobacco 0105 earth and related environmental sciences Principal Component Analysis Volatile Organic Compounds Chromatography Cigarette filter Chemistry 010401 analytical chemistry Organic Chemistry General Medicine 0104 chemical sciences Comprehensive two-dimensional gas chromatography Gas chromatography Gases |
Zdroj: | Journal of chromatography. A. 1525 |
ISSN: | 1873-3778 |
Popis: | A thermal desorption comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (TD-GC×GC-TOFMS) method has been developed for the analysis of mainstream tobacco smoke (MTS) vapour phase (VP). The selection process of the sample introduction approach involved comparing the results obtained from three different approaches: a) use of gas sampling bag followed by SPME (Tedlar®-SPME), b) gas sampling bag followed by TD (Tedlar®-TD), and c) sampling directly on TD sorbents (Direct-TD). Six different SPME fibers and six different TD sorbent beds were evaluated for the extraction capacities in terms of total number of peaks and related intensities or peak areas. The best results were obtained for the Direct-TD approach using Tenax TA/Carbograph1TD/Carboxen1003 sorbent tubes. The optimisation of TD tube desorption parameters was carried out using a face-centered central composite experimental design and resulted in the use of the Tenax TA/Carbograph 1TD/Carboxen 1003 sorbent with a 7.5min desorption time, a 60mL/min tube desorption flow, and a 250°C tube desorption temperature. The optimised method was applied to the separation of MTS-VP constituents, with 665 analytes detected. The method precision ranged from 1% to 15% for over 99% of identified peak areas and from 0% to 3% and 0% to 1% for both first (1tR) and second (2tR) dimension retention times, respectively. The method was applied to the analyses of two cigarette types differing in their filter construction. Principal component analysis (PCA) allowed a clear differentiation of the studied cigarette types (PC1 describing 94% of the explained variance). Supervised Fisher ratio analysis permitted the identification of compounds responsible for the chemical differences between the two sample types. A set of 91 most relevant compounds was selected by applying a Fisher ratio cut-off approach and most of them were selectively removed by one of the cigarette filter types. |
Databáze: | OpenAIRE |
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