Non-methane hydrocarbon (NMHC) fingerprints of major urban and agricultural emission sources for use in source apportionment studies

Ashish Kumar, Vinayak Sinha*, Muhammed Shabin, Haseeb Hakkim, Bernard Bonsang, Valerie Gros

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

In complex atmospheric emission environments such as urban agglomerates, multiple sources control the ambient chemical composition driving air quality and regional climate. In contrast to pristine sites, where reliance on single or a few chemical tracers is often adequate for resolving pollution plumes and source influences, the comprehensive chemical fingerprinting of sources using nonmethane hydrocarbons (NMHCs) and the identification of suitable tracer molecules and emission ratios becomes necessary. Here, we characterise and present chemical fingerprints of some major urban and agricultural emission sources active in South Asia, such as paddy stubble burning, garbage burning, idling vehicular exhaust and evaporative fuel emissions. A total of 121 whole air samples were actively collected from the different emission sources in passivated air sampling steel canisters and then analysed for 49 NMHCs (22 alkanes, 16 aromatics, 10 alkenes and one alkyne) using thermal desorption gas chromatography flame ionisation detection. Several new insights were obtained. Propane was found to be present in paddy stubble fire emissions (8 %), and therefore, for an environment impacted by crop residue fires, the use of propane as a fugitive liquefied petroleum gas (LPG) emission tracer must be done with caution. Propene was found to be ∼ 1.6 times greater (by weight) than ethene in smouldering paddy fires. Compositional differences were observed between evaporative emissions of domestic LPG and commercial LPG, which are used in South Asia. While the domestic LPG vapours had more propane (40 ± 6 %) than n-butane (19 ± 2 %), the converse was true for commercial LPG vapours (7 ± 6 % and 37 ± 4 %, respectively). Isoprene was identified as a new tracer for distinguishing paddy stubble and garbage burning in the absence of isoprene emissions at night from biogenic sources. Analyses of source-specific inter-NMHC molar ratios revealed that toluene/benzene ratios can be used to distinguish among paddy stubble fire emissions in the flaming (0.38 ± 0.11) and smouldering stages (1.40 ± 0.10), garbage burning flaming (0.26 ± 0.07) and smouldering emissions (0.59 ± 0.16), and traffic emissions (3.54 ± 0.21), whereas i-pentane = npentane can be used to distinguish biomass burning emissions (0.06 1.46) from the petrol-dominated traffic and fossil fuel emissions (2.83 4.13). i-butane = n-butane ratios were similar (0.20 0.30) for many sources and could be used as a tracer for photochemical ageing. In agreement with previous studies, i-pentane, propane and acetylene were identified as suitable chemical tracers for petrol vehicular and evaporative emissions, LPG evaporative and vehicular emissions and flaming-stage biomass fires, respectively. The secondary pollutant formation potential and human health impact of the sources was also assessed in terms of their hydroxyl radical (OH) reactivity (s-1), ozone formation potential (OFP; gO3/gNMHC) and fractional benzene, toluene, ethylbenzene and xylenes (BTEX) content. Petrol vehicular emissions, paddy stubble fires and garbage fires were found to have a higher pollution potential (at = 95 % confidence interval) relative to the other sources studied in this work. Thus, many results of this study provide a new foundational framework for quantitative source apportionment studies in complex emission environments.

Original languageEnglish
Pages (from-to)12133-12152
Number of pages20
JournalAtmospheric Chemistry and Physics
Volume20
Issue number20
DOIs
Publication statusPublished - 26 Oct 2020

Bibliographical note

© Author(s) 2020.

Funding Information:
Financial support. This research has been supported by the Na-

Funding Information:
Acknowledgements. We acknowledge the IISER Mohali Atmospheric Chemistry Facility for the data and the Ministry of Human Resource Development (MHRD), India, for funding the facility. Ashish Kumar, Haseeb Hakkim and Muhammed Shabin acknowledge MHRD and IISER Mohali for the doctoral (SRF and JRF) fellowships. We acknowledge EGU for the waiver of the APC through the EGU 2019 OSPP award to Ashish Kumar. We also thank Baer-bel Sinha (Department of Earth and Environmental Sciences, Indian Institute of Science Education and Research, Mohali) and the two anonymous reviewers for their helpful suggestions and insightful comments which helped to improve the paper. We also acknowledge the help and support of the members of IISER Mohali Atmospheric Chemistry facility, namely Harshita Pawar, Pallavi, Ab-hishek Mishra, Abhishek Verma, Bharti Sohpaul and Tess George for their technical assistance during field sampling.

Publisher Copyright:
© 2020 Author(s).

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