Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/80775
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorLyu, XPen_US
dc.creatorWang, Nen_US
dc.creatorGuo, Hen_US
dc.creatorXue, LKen_US
dc.creatorJiang, Fen_US
dc.creatorZeren, YZen_US
dc.creatorCheng, HRen_US
dc.creatorCai, Zen_US
dc.creatorHan, LHen_US
dc.creatorZhou, Yen_US
dc.date.accessioned2019-05-28T01:09:17Z-
dc.date.available2019-05-28T01:09:17Z-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/80775-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2019. This work is distributed underthe Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Lyu, X., Wang, N., Guo, H., Xue, L., Jiang, F., Zeren, Y., Cheng, H., Cai, Z., Han, L., and Zhou, Y.: Causes of a continuous summertime O3 pollution event in Jinan, a central city in the North China Plain, Atmos. Chem. Phys., 19, 3025-3042 is available at https://dx.doi.org/10.5194/acp-19-3025-2019en_US
dc.titleCauses of a continuous summertime O-3 pollution event in Jinan, a central city in the North China Plainen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3025en_US
dc.identifier.epage3042en_US
dc.identifier.volume19en_US
dc.identifier.issue5en_US
dc.identifier.doi10.5194/acp-19-3025-2019en_US
dcterms.abstractIn the summer of 2017, measurements of ozone (O-3) and its precursors were carried out at an urban site in Jinan, a central city in the North China Plain (NCP). A continuous O-3 pollution event was captured during 4-11 August, with the maximum hourly O-3 mixing ratio reaching 154.1 ppbv. Model simulation indicated that local photochemical formation and regional transport contributed 14.0 +/- 2.3 and 18.7 +/- 4.0 ppbv h(-1), respectively, to the increase in O-3 during 09:00-15:00 LT (local time) in this event. For local O-3 formation, the calculated OH reactivities of volatile organic compounds (VOCs) and carbon monoxide (CO) were comparable between O-3 episodes and non-episodes (p > 0.05), so was the OH reactivity of nitrogen oxides (NOx). However, the ratio of OH reactivity of VOCs and CO to that of NOx increased from 2.0 +/- 0.4 s(-1) s(1) during non-episodes to 3.7 +/- 0.7 s(-1) s(1) during O-3 episodes, which resulted in the change in the O-3 formation mechanism from the VOC-limited regime before the O-3 pollution event to the transitional regime during the event. Correspondingly, the simulated local O-3 production rate during the event (maximum: 21.3 ppbv h(-1)) was markedly higher than that before the event (p < 0.05) (maximum: 16.9 ppbv h(-1)). Given that gasoline and diesel exhaust made large contributions to the abundance of O-3 precursors and the O-3 production rate, constraint on vehicular emissions is the most effective strategy to control O-3 pollution in Jinan. The NCP has been confirmed as a source region of tropospheric O-3, where the shift in regimes controlling O-3 formation like the case presented in this study can be expected across the entire region, due to the substantial reductions of NOx emissions in recent years.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2019, v. 19, no. 5, p. 3025-3042en_US
dcterms.isPartOfAtmospheric chemistry and physicsen_US
dcterms.issued2019-
dc.identifier.isiWOS:000460817300002-
dc.identifier.eissn1680-7324en_US
dc.description.validate201905 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0563-n14-
dc.identifier.SubFormID259-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextRGC: PolyU5154/13E, PolyU152052/14E, PolyU152052/16E, CRF/C5004-15E and CRF/C5022-14G||Others: 2017YFC0212001; 4-ZZFW; G-YBUQ, 1-ZVJT; 1-BBW4en_US
dc.description.pubStatusPublisheden_US
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