Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/65656
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorTham, YJ-
dc.creatorWang, Z-
dc.creatorLi, Q-
dc.creatorYun, H-
dc.creatorWang, W-
dc.creatorWang, X-
dc.creatorXue, L-
dc.creatorLu, K-
dc.creatorMa, N-
dc.creatorBohn, B-
dc.creatorLi, X-
dc.creatorKecorius, S-
dc.creatorGröß, J-
dc.creatorShao, M-
dc.creatorWiedensohler, A-
dc.creatorZhang, Y-
dc.creatorWang, T-
dc.date.accessioned2017-05-22T02:09:00Z-
dc.date.available2017-05-22T02:09:00Z-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/65656-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2016. This is an open access article distributed under the Creative Commons Attribution 3.0 License (https://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication: Tham, Y. J., Wang, Z., Li, Q., Yun, H., Wang, W., Wang, X., Xue, L., Lu, K., Ma, N., Bohn, B., Li, X., Kecorius, S., Größ, J., Shao, M., Wiedensohler, A., Zhang, Y., and Wang, T.: Significant concentrations of nitryl chloride sustained in the morning: investigations of the causes and impacts on ozone production in a polluted region of northern China, Atmos. Chem. Phys., 16, 14959-14977 is available at https://doi.org/10.5194/acp-16-14959-2016, 2016.en_US
dc.titleSignificant concentrations of nitryl chloride sustained in the morning : investigations of the causes and impacts on ozone production in a polluted region of northern Chinaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage14959en_US
dc.identifier.epage14977en_US
dc.identifier.volume16en_US
dc.identifier.issue23en_US
dc.identifier.doi10.5194/acp-16-14959-2016en_US
dcterms.abstractNitryl chloride (ClNO2) is a dominant source of chlorine radical in polluted environment, and can significantly affect the atmospheric oxidative chemistry. However, the abundance of ClNO2 and its exact role are not fully understood under different environmental conditions. During the summer of 2014, we deployed a chemical ionization mass spectrometer to measure ClNO2 and dinitrogen pentoxide (N2O5) at a rural site in the polluted North China Plain. Elevated mixing ratios of ClNO2 (>350pptv) were observed at most of the nights with low levels of N2O5 (<200pptv). The highest ClNO2 mixing ratio of 2070pptv (1min average) was observed in a plume from a megacity (Tianjin), and was characterized with a faster N2O5 heterogeneous loss rate and ClNO2 production rate compared to average conditions. The abundant ClNO2 concentration kept increasing even after sunrise, and reached a peak 4h later. Such highly sustained ClNO2 peaks after sunrise are discrepant from the previously observed typical diurnal pattern. Meteorological and chemical analysis shows that the sustained ClNO2 morning peaks are caused by significant ClNO2 production in the residual layer at night followed by downward mixing after breakup of the nocturnal inversion layer in the morning. We estimated that ? 1.7-4.0ppbv of ClNO2 would exist in the residual layer in order to maintain the observed morning ClNO2 peaks at the surface site. Observation-based box model analysis show that photolysis of ClNO2 produced chlorine radical with a rate up to 1.12ppbvh?'1, accounting for 10-30% of primary ROxproduction in the morning hours. The perturbation in total radical production leads to an increase of integrated daytime net ozone production by 3% (4.3ppbv) on average, and with a larger increase of 13% (11ppbv) in megacity outflow that was characterized with higher ClNO2 and a relatively lower oxygenated hydrocarbon (OVOC) to non-methane hydrocarbon (NMHC) ratio.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2016, v. 16, no. 23, p. 14959-14977-
dcterms.isPartOfAtmospheric chemistry and physics-
dcterms.issued2016-
dc.identifier.isiWOS:000389208700002-
dc.identifier.scopus2-s2.0-85002739495-
dc.identifier.ros2016001449-
dc.identifier.eissn1680-7324en_US
dc.identifier.rosgroupid2016001423-
dc.description.ros2016-2017 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201811_a bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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