Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/7006
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorXue, L-
dc.creatorWang, T-
dc.creatorGuo, H-
dc.creatorBlake, DR-
dc.creatorTang, J-
dc.creatorZhang, XC-
dc.creatorSaunders, SM-
dc.creatorWang, WX-
dc.date.accessioned2014-12-11T08:26:56Z-
dc.date.available2014-12-11T08:26:56Z-
dc.identifier.issn1680-7316-
dc.identifier.urihttp://hdl.handle.net/10397/7006-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2013. This work is distributed under the Creative Commons Attribution 3.0 License.en_US
dc.subjectAir massen_US
dc.subjectAtmospheric chemistryen_US
dc.subjectAtmospheric pollutionen_US
dc.subjectConcentration (composition)en_US
dc.subjectHydrogen peroxideen_US
dc.subjectHydroxyl radicalen_US
dc.subjectLong range transporten_US
dc.subjectOzoneen_US
dc.subjectPhotochemistryen_US
dc.subjectPhotolysisen_US
dc.subjectSeasonal variationen_US
dc.subjectVolatile organic compounden_US
dc.titleSources and photochemistry of volatile organic compounds in the remote atmosphere of western China : results from the Mt. Waliguan Observatoryen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationAuthor name used in this publication: Xue, L. K.en_US
dc.description.otherinformationAuthor name used in this publication: Wang, T.en_US
dc.description.otherinformationAuthor name used in this publication: Guo, H.en_US
dc.identifier.spage8551-
dc.identifier.epage8567-
dc.identifier.volume13-
dc.identifier.issue17-
dc.identifier.doi10.5194/acp-13-8551-2013-
dcterms.abstractThe chemistry of the natural atmosphere and the influence by long-range transport of air pollution are key issues in the atmospheric sciences. Here we present two intensive field measurements of volatile organic compounds (VOCs) in late spring and summer of 2003 at Mt. Waliguan (WLG, 36.28°N, 100.90°E, 3816 m a.s.l.), a baseline station in the northeast part of the Qinghai-Tibetan Plateau. Most VOC species exhibited higher concentrations in late spring than in summer. A typical diurnal variation was observed with higher nighttime levels, in contrast to results from other mountainous sites. Five different air masses were identified from backward trajectory analysis showing distinct VOC speciation. Air masses originating from the central Eurasian continent contained the lowest VOC levels compared to the others that were impacted by anthropogenic emissions from China and the Indian subcontinent. A photochemical box model based on the Master Chemical Mechanism (version 3.2) and constrained by a full suite of measurements was developed to probe the photochemistry of atmosphere at WLG. Our results show net ozone production from in situ photochemistry during both late spring and summer. Oxidation of nitric oxide (NO) by the hydroperoxyl radical (HO₂) dominates the ozone production relative to the oxidation by the organic peroxy radicals (RO₂), and the ozone is primarily destroyed by photolysis and reactions with the HOₓ (HOₓ = OH + HO₂) radicals. Ozone photolysis is the predominant primary source of radicals (ROₓ = OH + HO₂ + RO₂), followed by the photolysis of secondary oxygenated VOCs and hydrogen peroxides. The radical losses are governed by the self and cross reactions among the radicals. Overall, the findings of the present study provide insights into the background chemistry and the impacts of pollution transport on the pristine atmosphere over the Eurasian continent.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2 Sept. 2013, v. 13, no. 17, p. 8551-8567-
dcterms.isPartOfAtmospheric chemistry and physics-
dcterms.issued2013-09-02-
dc.identifier.isiWOS:000324400600003-
dc.identifier.scopus2-s2.0-84883387666-
dc.identifier.eissn1680-7324-
dc.identifier.rosgroupidr70901-
dc.description.ros2013-2014 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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