光解
白天
对流层
化学
光化学
氧化剂
大气化学
大气(单位)
激进的
反应性(心理学)
微量气体
氮氧化物
粒子(生态学)
环境化学
惰性
化学反应
臭氧
矿物粉尘
二氧化氮
氨
反应速率常数
氰
亚硝酸
作者
Yiqun Cao,Huiying Xuan,Jun Liu,Hui Li,Peng Zhang,T X Chen,Yonghong Wang,Biwu Chu,Pengfei Liu,Yu Mu,Q L,H. He
标识
DOI:10.1021/acs.est.5c18673
摘要
H 2 O 2 is a vital atmospheric oxidant, while its photolysis in the troposphere is negligible in conventional view. For the first time, we find that gas-phase H 2 O 2 can undergo heterogeneous photolysis to produce OH radicals on the surfaces of particles such as SiO 2, Fe 2 O 3, and Na 2 SO 4 under solar irradiation, which further convert NO to produce HONO and NO 2 . It is demonstrated that acidity can inhibit the formation of HONO and promote the formation of NO 2 significantly. Moreover, the heterogeneous photolysis of H 2 O 2 is dependent on the reactivity of particles, with inert surfaces being more conducive to the generation of OH radicals. A MCM box model indicates that the HONO formation rate via the H 2 O 2 heterogeneous reaction can reach 0.10 ppb·h –1 at 9 a.m., and the relative contribution to the total daytime HONO production can account for approximately 5% at 1 p.m. Given the ubiquitous presence of SiO 2 in mineral dust particles, glass curtain walls, and terrestrial soils, these findings indicate that heterogeneous photolysis of H 2 O 2 on the particle surface could be a potential source of daytime HONO. Our research also underscores the importance of atmospheric interfacial chemistry and its contribution to unknown sources of atmospheric oxidizing capacity.
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