Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/61999
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorLing, Zen_US
dc.creatorGuo, Hen_US
dc.creatorChen, Gen_US
dc.creatorLam, SHMen_US
dc.creatorFan, Sen_US
dc.date.accessioned2016-12-19T08:58:07Z-
dc.date.available2016-12-19T08:58:07Z-
dc.identifier.issn1680-8584en_US
dc.identifier.urihttp://hdl.handle.net/10397/61999-
dc.language.isoenen_US
dc.publisherChinese Association for Aerosol Research in Taiwanen_US
dc.rightsCopyright © Taiwan Association for Aerosol Researchen_US
dc.rightsThis is an open access article under the CC-BY 4.0 license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.subjectCH3CHOen_US
dc.subjectHCHOen_US
dc.subjectHong Kongen_US
dc.subjectSource apportionmenten_US
dc.titleFormaldehyde and Acetaldehyde at different elevations in mountainous areas in Hong Kongen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1868en_US
dc.identifier.epage1878en_US
dc.identifier.volume16en_US
dc.identifier.issue8en_US
dc.identifier.doi10.4209/aaqr.2015.09.0571en_US
dcterms.abstractIntensive field measurements of formaldehyde (HCHO) and acetaldehyde (CH3CHO) were concurrently conducted at a mountain site (TMS) and an urban site (TW) at the foot of the same mountain in Hong Kong from September to November 2010. The spatiotemporal variations of HCHO and CH3CHO, the correlation between HCHO and CH3CHO and the ratios of HCHO/CH3CHO indicated different impacts of primary emissions and secondary formation at the two sites. The source apportionments of HCHO and CH3CHO at both sites were investigated using the Positive Matrix Factorization (PMF) model, while the in-situ formation of HCHO and CH3CHO was estimated using a Photochemical Box Model coupled with Master Chemical Mechanism (PBM-MCM). At TMS, the in-situ formation was the most significant contributor to ambient HCHO and CH3CHO, accounting for 51 ± 5 and 32 ± 2%, respectively, followed by the transport of photochemicallyformed aldehydes, vehicular emissions, biogenic emissions, biomass burning and solvent usage. On the other hand, at TW, the in-situ formation and vehicular emissions explained 55 ± 7% and 18 ± 1% of ambient HCHO, respectively, while vehicular emissions and in-situ formation made comparable contributions to CH3CHO (~35%). The findings are helpful for the formulation and implementation of appropriate control strategies for aldehydes and their precursors in Hong Kong.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAerosol and air quality research, Aug. 2016, v. 16, no. 8, p. 1868-1878en_US
dcterms.isPartOfAerosol and air quality researchen_US
dcterms.issued2016-08-
dc.identifier.isiWOS:000381982900007-
dc.identifier.scopus2-s2.0-84979903090-
dc.identifier.ros2016001613-
dc.identifier.rosgroupid2016001587-
dc.description.ros2016-2017 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201804_a bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberRGC-B1-077-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Sun Yat-sen Universityen_US
dc.description.pubStatusPublisheden_US
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