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The Chemistry of Mercury in the Stratosphere.
Saiz-Lopez, Alfonso; Acuña, A Ulises; Mahajan, Anoop S; Dávalos, Juan Z; Feng, Wuhu; Roca-Sanjuán, Daniel; Carmona-García, Javier; Cuevas, Carlos A; Kinnison, Douglas E; Gómez Martín, Juan Carlos; Francisco, Joseph S; Plane, John M C.
Afiliação
  • Saiz-Lopez A; Department of Atmospheric Chemistry and Climate Institute of Physical Chemistry Rocasolano CSIC Madrid Spain.
  • Acuña AU; Department of Atmospheric Chemistry and Climate Institute of Physical Chemistry Rocasolano CSIC Madrid Spain.
  • Mahajan AS; Centre for Climate Change Research Indian Institute of Tropical Meteorology Ministry of Earth Sciences Pune India.
  • Dávalos JZ; Department of Atmospheric Chemistry and Climate Institute of Physical Chemistry Rocasolano CSIC Madrid Spain.
  • Feng W; School of Chemistry University of Leeds Leeds UK.
  • Roca-Sanjuán D; NCAS School of Earth and Environment University of Leeds Leeds UK.
  • Carmona-García J; Institut de Ciència Molecular Universitat de València València Spain.
  • Cuevas CA; Department of Atmospheric Chemistry and Climate Institute of Physical Chemistry Rocasolano CSIC Madrid Spain.
  • Kinnison DE; Institut de Ciència Molecular Universitat de València València Spain.
  • Gómez Martín JC; Department of Atmospheric Chemistry and Climate Institute of Physical Chemistry Rocasolano CSIC Madrid Spain.
  • Francisco JS; Atmospheric Chemistry Observations and Modelling NCAR Boulder CO USA.
  • Plane JMC; Instituto de Astrofísica de Andalucía CSIC Granada Spain.
Geophys Res Lett ; 49(12): e2022GL097953, 2022 Jun 28.
Article em En | MEDLINE | ID: mdl-35860422
ABSTRACT
Mercury, a global contaminant, enters the stratosphere through convective uplift, but its chemical cycling in the stratosphere is unknown. We report the first model of stratospheric mercury chemistry based on a novel photosensitized oxidation mechanism. We find two very distinct Hg chemical regimes in the stratosphere in the upper stratosphere, above the ozone maximum concentration, Hg0 oxidation is initiated by photosensitized reactions, followed by second-step chlorine chemistry. In the lower stratosphere, ground-state Hg0 is oxidized by thermal reactions at much slower rates. This dichotomy arises due to the coincidence of the mercury absorption at 253.7 nm with the ozone Hartley band maximum at 254 nm. We also find that stratospheric Hg oxidation, controlled by chlorine and hydroxyl radicals, is much faster than previously assumed, but moderated by efficient photo-reduction of mercury compounds. Mercury lifetime shows a steep increase from hours in the upper-middle stratosphere to years in the lower stratosphere.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Geophys Res Lett Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Geophys Res Lett Ano de publicação: 2022 Tipo de documento: Article