Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/102605
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorMa, Qen_US
dc.creatorWang, Ten_US
dc.creatorLiu, Cen_US
dc.creatorHe, Hen_US
dc.creatorWang, Zen_US
dc.creatorWang, Wen_US
dc.creatorLiang, Yen_US
dc.date.accessioned2023-10-26T07:19:48Z-
dc.date.available2023-10-26T07:19:48Z-
dc.identifier.issn0013-936Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/102605-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2017 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Environmental science and technology, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.est.6b05724.en_US
dc.titleSO₂ initiates the efficient conversion of NO₂ to HONO on MgO surfaceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3767en_US
dc.identifier.epage3775en_US
dc.identifier.volume51en_US
dc.identifier.issue7en_US
dc.identifier.doi10.1021/acs.est.6b05724en_US
dcterms.abstractNitrous acid (HONO) is an important source of hydroxyl radical (OH) that determines the fate of many chemically active and climate relevant trace gases. However, the sources and the formation mechanisms of HONO remain poorly understood. In this study, the effect of SO2 on the heterogeneous reactions of NO2 on MgO as a mineral dust surrogate was investigated. The reactivity of MgO to NO2 is weak, while coexisting SO2 can increase the uptake coefficients of NO2 on MgO by 2-3 orders of magnitude. The uptake coefficients of NO2 on SO2-aged MgO are independent of NO2 concentrations in the range of 20-160 ppbv and relative humidity (0-70%RH). The reaction mechanism was demonstrated to be a redox reaction between NO2 and surface sulfite. In the presence of SO2, NO2 was reduced to nitrite under dry conditions, which could be further converted to gas-phase HONO in humid conditions. These results suggest that the reductive effect of SO2 on the heterogeneous conversion of NO2 to HONO may have a significant contribution to the unknown sources of HONO observed in polluted areas (for example, in China).en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationEnvironmental science and technology, 4 Apr. 2017, v. 51, no. 7, p. 3767-3775en_US
dcterms.isPartOfEnvironmental science and technologyen_US
dcterms.issued2017-04-04-
dc.identifier.scopus2-s2.0-85019766381-
dc.identifier.pmid28248489-
dc.identifier.eissn1520-5851en_US
dc.description.validate202310 bcchen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberCEE-2205-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Hong Kong Polytechnic University; Chinese Academy of Sciencesen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6748844-
dc.description.oaCategoryGreen (AAM)en_US
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