煤
北京
活性氧
环境科学
环境化学
气溶胶
煤燃烧产物
化学
作者
Kaining Zhao,Yuanxun Zhang,Jing Shang,James J. Schauer,Wei Huang,Jingyu Tian,Shujian Yang,Dongqing Fang,Dong Zhang
标识
DOI:10.1016/j.jes.2022.06.038
摘要
The Beijing “Coal to Electricity” program provides a unique opportunity to explore air quality impacts by replacing residential coal burning with electrical appliances. In this study, the atmospheric ROS (Gas-phase ROS and Particle-phase ROS, abbreviated to G-ROS and P-ROS) were measured by an online instrument in parallel with concurrent PM 2.5 sample collections analyzed for chemical composition and cellular ROS in a baseline year (Coal Use Year-CUY) and the first year following implementation of the “Coal to Electricity” program (Coal Ban Year-CBY). The results showed PM 2.5 concentrations had no significant difference between the two sampling periods, but the activities of G-ROS, P-ROS, and cellular ROS in CBY were 8.72 nmol H 2 O 2 /m 3 , 9.82 nmol H 2 O 2 /m 3 , and 2045.75 μg UD /mg PM higher than in CUY. Six sources were identified by factor-analysis from the chemical components of PM 2.5 . Secondary sources (SECs) were the dominant source of PM 2.5 in the two periods, with 15.90% higher contribution in CBY than in CUY. Industrial Emission & Coal Combustion sources (Ind. & CCs), mainly from regional transport, also increased significantly in CBY. The contributions of Aged Sea Salt & Residential Burning sources to PM 2.5 decreased 5.31% from CUY to CBY. The correlation results illustrated that Ind. & CCs had significant positive correlations with atmospheric ROS, and SECs significantly associated with cellular ROS, especially nitrates ( r = 0.626, p = 0.000). Therefore, the implementation of the “Coal to Electricity” program reduced PM 2.5 contributions from coal and biomass combustion, but had little effect on the improvement of atmospheric and cellular ROS.
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