光解
反应速率常数
化学
光化学
催化作用
产量(工程)
动力学
硝酸
反应机理
基质(化学分析)
氮氧化物
无机化学
有机化学
材料科学
色谱法
燃烧
物理
量子力学
冶金
作者
Chunxiang Ye,Ning Zhang,H. Gao,Xianliang Zhou
标识
DOI:10.1038/s41598-018-37973-x
摘要
Abstract Photolysis rate constant of HNO 3 on the surface (HNO 3(s) ) has been found to be enhanced by 1–4 orders of magnitude from that of gaseous HNO 3 , with HONO and NO 2 as the main products. Such Re-NOx-ification pathway extends the apparent lifetime of reactive nitrogen species and modifies the atmospheric oxidative capacity along its long-rang transport. Despite of its importance, the detailed kinetics and mechanisms of HNO 3(s) photolysis are still not clear. Surface film of HNO 3 and organic compounds is ubiquitous in the environment and imposes matrix effect on HNO 3(s) photolysis. Here we studied photolysis of HNO 3 on Pyrex glass in a photochemical flow reactor over a wide range of HNO 3 surface density ( D HNO3 ) with or without the presence of model organic compounds. The photolysis rate constant of HNO 3(s) varied with D HNO3 and surface-catalysis mechanism was proposed. Organic compounds further enhance the photolysis rate constant by up to one order of magnitude via both photosensitization and H-donating reaction. The H-donating reaction enhances as well the secondary HONO yield from reaction between the primary product NO 2 and adjacent H-donor, and thus increases the HONO/NO 2 production ratio. Finally, detailed mechanisms involving surface-catalyisis, photosensitization and H-donating reactions was integrated.
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