Chenyang Du, Hongli Wang*, Yaqin Gao, Rusha Yan, Sheng’ao Jing, Min Zhou, Qian Wang, Shengrong Lou, Cheng Huang, Dan Dan Huang, Yu Shang* and Jing An,
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Observation-constrained dilution and entrainment substantially reduced simulated HCHO levels, but failed to capture the observed diurnal patterns. Incorporating reactive uptake onto aerosol liquid water effectively matched the observed secondary production component during colder months, but remained insufficient to fully address the overestimation in summer. Further analysis identified isoprene photochemistry as the major secondary source of summertime HCHO, with its yield highly sensitive to subppb levels of nitric oxides (NO), where the recently discovered isoprene peroxy interconversion competitively regulates the carbon flow that leads to HCHO. Scaling NO measurements notably improved model performance, underscoring the importance of subppb NO data and refined chemical mechanisms in representing HCHO dynamics in urban centers with steadily improved air quality.</p>","PeriodicalId":15,"journal":{"name":"ACS Earth and Space Chemistry","volume":"9 5","pages":"1174–1184 1174–1184"},"PeriodicalIF":2.9000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Processes Driving Diurnal and Seasonal Variations of Formaldehyde in an Urban Environment\",\"authors\":\"Chenyang Du, Hongli Wang*, Yaqin Gao, Rusha Yan, Sheng’ao Jing, Min Zhou, Qian Wang, Shengrong Lou, Cheng Huang, Dan Dan Huang, Yu Shang* and Jing An, \",\"doi\":\"10.1021/acsearthspacechem.5c0002010.1021/acsearthspacechem.5c00020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >This study aims to elucidate the physicochemical processes driving the persistently elevated levels of formaldehyde (HCHO) in Shanghai, the largest megacity in China. Field measurements combined with statistical analyses revealed that primary sources remained consistently prominent throughout the year, while secondary production exhibited pronounced seasonal variation. A process-level box model was employed to deconvolute the contributions of secondary production pathways to the temporal variability of HCHO. A sequence of physical removal schemes was integrated into the model framework to resolve the overestimation of HCHO across all seasons in the base configuration. Observation-constrained dilution and entrainment substantially reduced simulated HCHO levels, but failed to capture the observed diurnal patterns. Incorporating reactive uptake onto aerosol liquid water effectively matched the observed secondary production component during colder months, but remained insufficient to fully address the overestimation in summer. Further analysis identified isoprene photochemistry as the major secondary source of summertime HCHO, with its yield highly sensitive to subppb levels of nitric oxides (NO), where the recently discovered isoprene peroxy interconversion competitively regulates the carbon flow that leads to HCHO. Scaling NO measurements notably improved model performance, underscoring the importance of subppb NO data and refined chemical mechanisms in representing HCHO dynamics in urban centers with steadily improved air quality.</p>\",\"PeriodicalId\":15,\"journal\":{\"name\":\"ACS Earth and Space Chemistry\",\"volume\":\"9 5\",\"pages\":\"1174–1184 1174–1184\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Earth and Space Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsearthspacechem.5c00020\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Earth and Space Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsearthspacechem.5c00020","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Processes Driving Diurnal and Seasonal Variations of Formaldehyde in an Urban Environment
This study aims to elucidate the physicochemical processes driving the persistently elevated levels of formaldehyde (HCHO) in Shanghai, the largest megacity in China. Field measurements combined with statistical analyses revealed that primary sources remained consistently prominent throughout the year, while secondary production exhibited pronounced seasonal variation. A process-level box model was employed to deconvolute the contributions of secondary production pathways to the temporal variability of HCHO. A sequence of physical removal schemes was integrated into the model framework to resolve the overestimation of HCHO across all seasons in the base configuration. Observation-constrained dilution and entrainment substantially reduced simulated HCHO levels, but failed to capture the observed diurnal patterns. Incorporating reactive uptake onto aerosol liquid water effectively matched the observed secondary production component during colder months, but remained insufficient to fully address the overestimation in summer. Further analysis identified isoprene photochemistry as the major secondary source of summertime HCHO, with its yield highly sensitive to subppb levels of nitric oxides (NO), where the recently discovered isoprene peroxy interconversion competitively regulates the carbon flow that leads to HCHO. Scaling NO measurements notably improved model performance, underscoring the importance of subppb NO data and refined chemical mechanisms in representing HCHO dynamics in urban centers with steadily improved air quality.
期刊介绍:
The scope of ACS Earth and Space Chemistry includes the application of analytical, experimental and theoretical chemistry to investigate research questions relevant to the Earth and Space. The journal encompasses the highly interdisciplinary nature of research in this area, while emphasizing chemistry and chemical research tools as the unifying theme. The journal publishes broadly in the domains of high- and low-temperature geochemistry, atmospheric chemistry, marine chemistry, planetary chemistry, astrochemistry, and analytical geochemistry. ACS Earth and Space Chemistry publishes Articles, Letters, Reviews, and Features to provide flexible formats to readily communicate all aspects of research in these fields.