Journal
CHEMOSPHERE
Volume 89, Issue 11, Pages 1407-1413Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2012.06.005
Keywords
Compound specific isotope analysis; Thermal desorption; Industry emission; Biomass combustion; Car exhaust emission; Source characterisation
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Funding
- Co-operative Research Centre for Contamination Assessment and Remediation of the Environment Pty Ltd. (CRC CARE)
- Institute for Geoscience Research (TIGeR) and Curtin
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This study presents carbon (delta C-13) and hydrogen (delta D) isotope values of volatile organic compounds (VOCs) in various emission sources using thermal desorption-gas chromatography-isotope ratio mass spectrometry (TD-GC-irMS). The investigated VOCs ranged from C6 to C10. Samples were taken from (i) car exhaust emissions as well as from plant combustion experiments of (ii) various C3 and (iii) various C4 plants. We found significant differences in delta values of analysed VOCs between these sources, e.g. delta C-13 of benzene ranged between (i) -21.7 +/- 0.2 parts per thousand, (ii) -27.6 +/- 1.6 parts per thousand and (iii) -16.3 +/- 2.2 parts per thousand, respectively and delta D of benzene ranged between (i) -73 +/- 13 parts per thousand, (ii) -111 +/- 10 parts per thousand and (iii) -70 +/- 24 parts per thousand, respectively. Results of VOCs present in investigated emission sources were compared to values from the literature (aluminium refinery emission). All source groups could be clearly distinguished using the dual approach of delta C-13 and delta D analysis. The results of this study indicate that the correlation of compound specific carbon and hydrogen isotope analysis provides the potential for future research to trace the fate and to determine the origin of VOCs in the atmosphere using thermal desorption compound specific isotope analysis. (C) 2012 Elsevier Ltd. All rights reserved.
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