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Hygroscopic Coating of Sulfuric Acid Shields Oxidant Attack on the Atmospheric Pollutant Benzo(a)pyrene Bound to Model Soot Particles

Substantial impacts on climate have been documented for soot‒sulfuric acid (H(2)SO(4)) interactions in terms of optical and hygroscopic properties of soot aerosols. However, the influence of H(2)SO(4) on heterogeneous chemistry on soot remains unexplored. Additionally, oxidation rate coefficients fo...

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Detalles Bibliográficos
Autores principales: Ray, Debajyoti, Bhattacharya, Tara Shankar, Chatterjee, Abhijit, Singha, Achintya, Ghosh, Sanjay K., Raha, Sibaji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760694/
https://www.ncbi.nlm.nih.gov/pubmed/29317668
http://dx.doi.org/10.1038/s41598-017-18292-z
Descripción
Sumario:Substantial impacts on climate have been documented for soot‒sulfuric acid (H(2)SO(4)) interactions in terms of optical and hygroscopic properties of soot aerosols. However, the influence of H(2)SO(4) on heterogeneous chemistry on soot remains unexplored. Additionally, oxidation rate coefficients for polycyclic aromatic hydrocarbons intrinsic to the atmospheric particles evaluated in laboratory experiments seem to overestimate their degradation in ambient atmosphere, possibly due to matrix effects which are hitherto not mimicked in laboratory experiments. For the first time, our kinetics study reports significant influence of H(2)SO(4) coating on heterogeneous ozonation of benzo(a)pyrene (BaP) deposited on model soot, representative to atmospheric particles. The approximate specific surface area of model soot (5 m(2)g(−1)) was estimated as a measure of the availability of surface molecules to a typical gaseous atmospheric oxidant. Heterogeneous bimolecular reaction kinetics and Raman spectroscopy studies suggested plausible reasons for decreased BaP ozonation rate in presence of H(2)SO(4): 1. decreased partitioning of O(3) on soot surface and 2. shielding of BaP molecules to gaseous O(3) by acid-BaP reaction or O(3) oxidation products.