Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/105157
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorZou, Zen_US
dc.creatorChen, Qen_US
dc.creatorXia, Men_US
dc.creatorYuan, Qen_US
dc.creatorChen, Yen_US
dc.creatorWang, Yen_US
dc.creatorXiong, Een_US
dc.creatorWang, Zen_US
dc.creatorWang, Ten_US
dc.date.accessioned2024-04-03T07:31:49Z-
dc.date.available2024-04-03T07:31:49Z-
dc.identifier.citationv. 23, no. 12, p. 7057-7074-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/105157-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2023. This work is distributed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Zou, Z., Chen, Q., Xia, M., Yuan, Q., Chen, Y., Wang, Y., Xiong, E., Wang, Z., & Wang, T. (2023). OH measurements in the coastal atmosphere of South China: possible missing OH sinks in aged air masses. Atmos. Chem. Phys., 23(12), 7057-7074 is available at https://dx.doi.org/10.5194/acp-23-7057-2023.en_US
dc.titleOH measurements in the coastal atmosphere of South China : possible missing OH sinks in aged air massesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage7057en_US
dc.identifier.epage7074en_US
dc.identifier.volume23en_US
dc.identifier.issue12en_US
dc.identifier.doi10.5194/acp-23-7057-2023en_US
dcterms.abstractThe hydroxyl radical (OH) is the main atmospheric oxidant responsible for the removal of many reduced trace gases and the formation of secondary air pollutants. However, due to technical difficulties in measuring OH, the existing measurements of atmospheric OH concentrations are limited, and its sources and sinks are not well understood under low-nitrogen-oxide (NOx ) conditions. In this study, we observed the OH concentrations using chemical ionization mass spectrometry at a coastal site in Hong Kong from October to November 2020. The average noontime OH concentration over the study period was measured at 4.9 ± 2.1 × 106 cm−3. We found that a box model with comprehensive observational constraints reproduced the observed daytime OH concentrations when air parcels originated from the continental regions. However, this model overpredicted the observed daytime OH concentrations for coastal air parcels by 142 % on average. Unaccounted-for OH sinks in the model are proposed to be the cause of this overprediction. A missing OH reactivity, which is defined as the pseudo-first-order rate coefficient for OH loss by unmeasured trace gases, was estimated as 5.0 ± 2.6 s−1 (lower limit) in the coastal air, and the missing reactivity increased with decreasing concentrations of NOx and volatile organic compounds (VOCs). Further studies are needed to find out the exact cause of the model overestimation and to identify the suspected unmeasured chemical species that contribute to the OH budget, in order to better quantify the formation of secondary air pollutants.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2023, v. 23, no. 12, p. 7057–7074en_US
dcterms.isPartOfAtmospheric chemistry and physicsen_US
dcterms.issued2023-
dc.identifier.eissn1680-7324en_US
dc.description.validate202404 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2666-n01-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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