北京
图层(电子)
残余物
硫酸盐
环境科学
化学
材料科学
纳米技术
中国
计算机科学
地理
有机化学
算法
考古
作者
Pengfei Liu,Shuyuan Jia,Shuying Li,Pengkun Ma,Yongjing Ma,Yuan Liu,Zhiheng Liao,Yonghong Wang,Biwu Chu,Qingxin Ma,Jiannong Quan,Yujing Mu,Hong He
标识
DOI:10.1021/acs.est.4c09004
摘要
Hydrogen peroxide (H2O2) plays a key role in atmospheric chemistry, but knowledge of its variation, sources, and impact on sulfate formation remains incomplete, especially in the urban boundary layer aloft. Here, we conducted a field campaign with measurements of H2O2 and related species at a tower-based site (∼528 m above the ground surface) of Beijing in spring of 2022. The observed hourly H2O2 concentration reached up to 21.2 ppbv with an average value of 3.4 ± 3.7 ppbv during the entire observation period, which was higher than values from previous observations throughout the world. The H2O2 budget revealed that the two known sources (self-reaction of HO2 radicals and ozonolysis of alkenes) could not account for the significant formation of H2O2, leading to a considerable unknown source strength (∼0.14–0.53 ppbv h–1) of H2O2 at noon and after sunset. Based on the levoglucosan signal, distribution of fire points, and backward trajectories, biomass burning emissions from the southwest of Beijing (e.g., North China Plain) were found to contribute greatly to H2O2 formation. Besides, photochemical aging of PM2.5 might also have a potential impact on H2O2 production at noon. The unexpectedly high concentrations of H2O2 aloft made a vital contribution to sulfate production (0.2–1.1 μg m–3 h–1), which could be transported to the ground surface during the turbulent mixing. Our findings provide an improved understanding of the H2O2 chemistry in the boundary layer aloft in a megacity, as well as its impact on sulfate formation.
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