Toward a better understanding of ferric-oxalate complex photolysis: The role of the aqueous/air interface of droplet

Autor: Yu Wang, Wenbo Dong, Yanlin Wu, Marcello Brigante, David Talaga, Sophie Sobanska, Gilles Mailhot
Přispěvatelé: Beijing Jiaotong University (BJTU), Institut de Chimie de Clermont-Ferrand (ICCF), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne (UCA)-Institut national polytechnique Clermont Auvergne (INP Clermont Auvergne), Université Clermont Auvergne (UCA)-Université Clermont Auvergne (UCA), Institut des Sciences Moléculaires (ISM), Université Montesquieu - Bordeaux 4-Université Sciences et Technologies - Bordeaux 1 (UB)-École Nationale Supérieure de Chimie et de Physique de Bordeaux (ENSCPB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of EnvFemental Science & Engineering, Fudan University, Shanghai Institute of Pollution Control and Ecological Security, Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 (LASIRE), Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2021
Předmět:
Zdroj: Chemosphere
Chemosphere, 2022, 289, pp.133127. ⟨10.1016/j.chemosphere.2021.133127⟩
ISSN: 1879-1298
0045-6535
DOI: 10.1016/j.chemosphere.2021.133127⟩
Popis: International audience; In this work, the photo reactivity of ferric oxalate (Fe(III)-Ox) complex in atmospheric particles was investigated. Raman spectroscopy was used to explore the mechanism and kinetics of Fe(III)-Ox photolysis occurring at the aqueous/gas interface, inside the droplet and in bulk solution. Ferrous carbonate (FeCO3) was detected indicating that carbonate ion (CO32−) formed inside the droplets would compete with oxalate ligands for iron complexation. A higher concentration of photoproduct Fe(II)-Ox was observed at the surface and inside of the droplets than in bulk solution. In particular, Fe(III)-Ox on the droplet surface was quickly reduced with light and Fe(II)-Ox concentration gradually decreased with irradiation time. The evolution of Fe(II)-Ox concentration was similar inside the droplet and in bulk solution with a trend of first increasing and then gradually decreasing during irradiation time. Although FeCO3 would hinder Fenton intermediate reaction, the photolysis rate of Fe(III)-Ox in droplets was almost two orders of magnitude times faster than that observed during bulk experiment. In general, the photolysis mechanism and kinetics of Fe(III)-Ox in aqueous/air interface, inside of droplet and bulk solution were distinct, and the production of oxide species from the atmospheric Fe(III)-Ox droplets was underestimated.
Databáze: OpenAIRE