Lourenço, Célia, González-Méndez, Ramón, Reich, Fraser, Mason, Nigel, Turner, Claire (2017) A potential method for comparing instrumental analysis of volatile organic compounds using standards calibrated for the gas phase. International Journal of Mass Spectrometry, 419 . pp. 1-10. ISSN 1387-3806. (doi:10.1016/j.ijms.2017.05.011) (KAR id:74646)
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Official URL: https://dx.doi.org/10.1016/j.ijms.2017.05.011 |
Abstract
In this paper we report a method for the comparative analysis of volatile organic compounds (VOCs) at physiologically representative concentrations by different analytical methods Standard aqueous solutions of acetone, ethanol, methanol, 1-propanol, 2-propanol and acetaldehyde were prepared by adding a specific mass of compound to a known volume of water, calculated using published Henry's law constants for individual compounds. Headspace concentrations are thus known from established partitioning from dilute aqueous phase in accordance with Henry's law. Selected Ion Flow Tube Mass Spectrometry (SIFT-MS), Proton Transfer Reaction Mass Spectrometry (PTR-MS), and Gas Chromatography–Mass Spectrometry (GC–MS) coupled to thermal desorption have been used to study and evaluate the performance of the instruments in the analysis of these VOCs. These analytical techniques have been widely used in the identification and quantification of trace concentrations of VOCs in biological samples. Quantitative determination of VOC concentration was achieved and the performance of the instruments compared with one another. Calibration curves are given within the range 101–103 ppbv.
Item Type: | Article |
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DOI/Identification number: | 10.1016/j.ijms.2017.05.011 |
Uncontrolled keywords: | GC–MS, Proton transfer reaction mass spectrometry, PTR-MS, Selected ion flow tube mass spectrometry, SIFT-MS, Trace gas analysis |
Subjects: | Q Science |
Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
Depositing User: | Nigel Mason |
Date Deposited: | 28 Jun 2019 12:55 UTC |
Last Modified: | 05 Nov 2024 12:37 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/74646 (The current URI for this page, for reference purposes) |
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