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

机译:硫酸的吸湿涂层屏蔽了对大气污染物苯并(a)re的氧化作用从而模拟了烟尘颗粒

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摘要

Substantial impacts on climate have been documented for soot‒sulfuric acid (H2SO4) interactions in terms of optical and hygroscopic properties of soot aerosols. However, the influence of H2SO4 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 H2SO4 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 m2g−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 H2SO4: 1. decreased partitioning of O3 on soot surface and 2. shielding of BaP molecules to gaseous O3 by acid-BaP reaction or O3 oxidation products.
机译:从烟尘气溶胶的光学和吸湿特性来看,烟‒硫酸(H2SO4)相互作用已对气候产生重大影响。但是,H2SO4对烟尘异质化学的影响尚待探索。另外,在实验室实验中评估的大​​气颗粒所固有的多环芳烃的氧化速率系数似乎高估了其在环境大气中的降解,这可能是由于迄今为止在实验室实验中未模仿的基质效应。我们的动力学研究首次报告了H2SO4涂层对沉积在模型烟灰上的苯并(a)re(BaP)的异质臭氧化的重大影响,代表大气颗粒。估计了模型烟灰的近似比表面积(5 m 2 g -1 ),以衡量表面分子对典型的气态氧化剂的有效性。异质双分子反应动力学和拉曼光谱研究表明,存在H2SO4时BaP臭氧化速率降低的合理原因:1.烟灰表面O3的分配减少;以及2.BaP分子被酸-BaP反应或O3氧化产物屏蔽为气态O3。

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