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Aromatic Photo-oxidation, A New Source of Atmospheric Acidity.
Wang, Sainan; Newland, Mike J; Deng, Wei; Rickard, Andrew R; Hamilton, Jacqueline F; Muñoz, Amalia; Ródenas, Milagros; Vázquez, Monica M; Wang, Liming; Wang, Xinming.
Afiliação
  • Wang S; State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China.
  • Newland MJ; Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, York YO10 5DD, U.K.
  • Deng W; State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China.
  • Rickard AR; Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, York YO10 5DD, U.K.
  • Hamilton JF; National Centre for Atmospheric Science, Wolfson Atmospheric Chemistry Laboratories, University of York, York YO10 5DD, U.K.
  • Muñoz A; Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, York YO10 5DD, U.K.
  • Ródenas M; Fundación CEAM, EUPHORE Laboratories, Avda. Charles R. Darwin. Parque Tecnológico, Paterna, Valencia, Spain.
  • Vázquez MM; Fundación CEAM, EUPHORE Laboratories, Avda. Charles R. Darwin. Parque Tecnológico, Paterna, Valencia, Spain.
  • Wang L; Fundación CEAM, EUPHORE Laboratories, Avda. Charles R. Darwin. Parque Tecnológico, Paterna, Valencia, Spain.
  • Wang X; School of Chemistry & Chemical Engineering, South China University of Technology, Guangzhou, China.
Environ Sci Technol ; 54(13): 7798-7806, 2020 07 07.
Article em En | MEDLINE | ID: mdl-32479720
ABSTRACT
Formic acid (HCOOH), one of the most important and ubiquitous organic acids in the Earth's atmosphere, contributes substantially to atmospheric acidity and affects pH-dependent reactions in the aqueous phase. However, based on the current mechanistic understanding, even the most advanced chemical models significantly underestimate the HCOOH concentrations when compared to ambient observations at both ground-level and high altitude, thus underrating its atmospheric impact. Here we reveal new chemical pathways to HCOOH formation from reactions of both O3 and OH with ketene-enols, which are important and to date undiscovered intermediates produced in the photo-oxidation of aromatics and furans. We highlight that the estimated yields of HCOOH from ketene-enol oxidation are up to 60% in polluted urban areas and greater than 30% even in the continental background. Our theoretical calculations are further supported by a chamber experiment evaluation. Considering that aromatic compounds are highly reactive and contribute ca. 10% to global nonmethane hydrocarbon emissions and 20% in urban areas, the new oxidation pathways presented here should help to narrow the budget gap of HCOOH and other small organic acids and can be relevant in any environment with high aromatic emissions, including urban areas and biomass burning plumes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Orgânicos / Atmosfera Idioma: En Revista: Environ Sci Technol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Orgânicos / Atmosfera Idioma: En Revista: Environ Sci Technol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China