Laijin Zhong , Bao Zhu , Wenyuan Su , Wenqing Liang , Haotian Wang , Tingyu Li , Dong Cao , Ting Ruan , Jianmin Chen , Guibin Jiang
{"title":"不同醌类似物在气溶胶结合的持久热解和光解自由基鉴别中的分子表征","authors":"Laijin Zhong , Bao Zhu , Wenyuan Su , Wenqing Liang , Haotian Wang , Tingyu Li , Dong Cao , Ting Ruan , Jianmin Chen , Guibin Jiang","doi":"10.1016/j.scib.2023.12.011","DOIUrl":null,"url":null,"abstract":"<div><p><span>Aerosol-bound organic radicals, including environmentally persistent free radicals<span><span> (EPFRs), are key components that affect climate, air quality, and human health. While putative structures have been proposed, the molecular characteristics of EPFRs remain unknown. Here, we report a surrogate method to characterize EPFRs in real ambient samples using </span>mass spectrometry<span>. The method identifies chemically relevant oxygenated polycyclic aromatic hydrocarbons (O</span></span></span><em><sub>x</sub></em>PAH) that interconvert with oxygen-centered EPFR (OC-EPFR). We found O<em><sub>x</sub></em><span>PAH compounds most relevant to OC-EPFRs are structurally rich and diverse quinones<span>, whose diversity is strongly associated with OC-EPFR levels. Both atmospheric oxidation and combustion contributed to OC-EPFR formation. Redundancy analysis and photochemical aging model show pyrolytic sources generated more oxidized OC-EPFRs than photolytic sources. Our study reveals the detailed molecular characteristics of OC-EPFRs and shows that oxidation states can be used to identify the origins of OC-EPFRs, offering a way to track the development and evolution of aerosol particles in the environment.</span></span></p></div>","PeriodicalId":421,"journal":{"name":"Science Bulletin","volume":"69 5","pages":"Pages 612-620"},"PeriodicalIF":18.8000,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular characterization of diverse quinone analogs for discrimination of aerosol-bound persistent pyrolytic and photolytic radicals\",\"authors\":\"Laijin Zhong , Bao Zhu , Wenyuan Su , Wenqing Liang , Haotian Wang , Tingyu Li , Dong Cao , Ting Ruan , Jianmin Chen , Guibin Jiang\",\"doi\":\"10.1016/j.scib.2023.12.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Aerosol-bound organic radicals, including environmentally persistent free radicals<span><span> (EPFRs), are key components that affect climate, air quality, and human health. While putative structures have been proposed, the molecular characteristics of EPFRs remain unknown. Here, we report a surrogate method to characterize EPFRs in real ambient samples using </span>mass spectrometry<span>. The method identifies chemically relevant oxygenated polycyclic aromatic hydrocarbons (O</span></span></span><em><sub>x</sub></em>PAH) that interconvert with oxygen-centered EPFR (OC-EPFR). We found O<em><sub>x</sub></em><span>PAH compounds most relevant to OC-EPFRs are structurally rich and diverse quinones<span>, whose diversity is strongly associated with OC-EPFR levels. Both atmospheric oxidation and combustion contributed to OC-EPFR formation. Redundancy analysis and photochemical aging model show pyrolytic sources generated more oxidized OC-EPFRs than photolytic sources. Our study reveals the detailed molecular characteristics of OC-EPFRs and shows that oxidation states can be used to identify the origins of OC-EPFRs, offering a way to track the development and evolution of aerosol particles in the environment.</span></span></p></div>\",\"PeriodicalId\":421,\"journal\":{\"name\":\"Science Bulletin\",\"volume\":\"69 5\",\"pages\":\"Pages 612-620\"},\"PeriodicalIF\":18.8000,\"publicationDate\":\"2023-12-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Bulletin\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2095927323008538\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Bulletin","FirstCategoryId":"103","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095927323008538","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Molecular characterization of diverse quinone analogs for discrimination of aerosol-bound persistent pyrolytic and photolytic radicals
Aerosol-bound organic radicals, including environmentally persistent free radicals (EPFRs), are key components that affect climate, air quality, and human health. While putative structures have been proposed, the molecular characteristics of EPFRs remain unknown. Here, we report a surrogate method to characterize EPFRs in real ambient samples using mass spectrometry. The method identifies chemically relevant oxygenated polycyclic aromatic hydrocarbons (OxPAH) that interconvert with oxygen-centered EPFR (OC-EPFR). We found OxPAH compounds most relevant to OC-EPFRs are structurally rich and diverse quinones, whose diversity is strongly associated with OC-EPFR levels. Both atmospheric oxidation and combustion contributed to OC-EPFR formation. Redundancy analysis and photochemical aging model show pyrolytic sources generated more oxidized OC-EPFRs than photolytic sources. Our study reveals the detailed molecular characteristics of OC-EPFRs and shows that oxidation states can be used to identify the origins of OC-EPFRs, offering a way to track the development and evolution of aerosol particles in the environment.
期刊介绍:
Science Bulletin (Sci. Bull., formerly known as Chinese Science Bulletin) is a multidisciplinary academic journal supervised by the Chinese Academy of Sciences (CAS) and co-sponsored by the CAS and the National Natural Science Foundation of China (NSFC). Sci. Bull. is a semi-monthly international journal publishing high-caliber peer-reviewed research on a broad range of natural sciences and high-tech fields on the basis of its originality, scientific significance and whether it is of general interest. In addition, we are committed to serving the scientific community with immediate, authoritative news and valuable insights into upcoming trends around the globe.