Characterization of photochemical losses of volatile organic compounds and their implications for ozone formation potential and source apportionment during summer in suburban Jinan, China

被引:9
|
作者
Liu, Zhenguo [1 ]
Wang, Baolin [1 ]
Wang, Chen [1 ]
Sun, Yuchun [1 ]
Zhu, Chuanyong [1 ]
Sun, Lei [1 ]
Yang, Na [1 ]
Fan, Guolan [2 ]
Sun, Xiaoyan [2 ]
Xia, Zhiyong [2 ]
Pan, Guang [2 ]
Zhu, Changtong [1 ]
Gai, Yichao [1 ]
Wang, Xiaoyu [1 ]
Xiao, Yang [3 ]
Yan, Guihuan [4 ]
Xu, Chongqing [1 ,4 ]
机构
[1] Qilu Univ Technol, Shandong Acad Sci, Sch Environm Sci & Engn, Jinan 250353, Peoples R China
[2] Jinan Ecoenvironm Monitoring Ctr Shandong Prov, Jinan 250101, Peoples R China
[3] Zibo Ecoenvironm Monitoring Ctr Shandong Prov, Zibo 255000, Peoples R China
[4] Qilu Univ Technol, Ecol Inst, Shandong Acad Sci, Jinan 250103, Peoples R China
基金
中国国家自然科学基金;
关键词
Volatile organic compounds; Photochemical losses; Ozone formation potential; Source apportionment; COMPOUNDS VOCS; CHEMICAL LOSS; HYDROCARBON; REACTIVITY; EMISSIONS; POLLUTION; MODEL; SITE;
D O I
10.1016/j.envres.2023.117158
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Volatile organic compounds (VOCs) undergo substantial photochemical losses during their transport from emission sources to receptor sites, resulting in serious implications for their source apportionment and ozone (O3) formation. Based on the continuous measurements of VOCs in suburban Jinan in August 2022, the effects of photochemical losses on VOC source contributions and O3 formation were evaluated in this study. The observed and initial concentrations of total VOCs (TVOC) were 12.0 +/- 5.1 and 16.0 +/- 7.4 ppbv, respectively. Throughout the observation period, alkenes had the most prominent photochemical losses (58.2%), followed by aromatic hydrocarbons (23.1%), accounting for 80.6% and 6.9% of the total losses, respectively. During high O3 episodes, the photochemical loss of VOCs was 6.9 times higher than that during the cleaning period. Alkene losses (exceeding 67.3%), specifically losses of isoprene, propylene, ethylene, and n-butene, dominated the total losses of VOCs during the O3 increase period. Eight sources of VOCs were identified by positive matrix factorization (PMF) based on the observed and initial concentration data (OC-PMF and IC-PMF, respectively). Concentrations of all emission sources in the OC-PMF were underestimated by 2.4%-57.1%. Moreover, the contribution of each emission source was over- or underestimated compared with that in case of the IC-PMF. The contributions of biogenic and motor vehicle exhaust emissions were underestimated by 5.3 and 2.8 percentage points, respectively, which was associated with substantial oxidation of the emitted high-reactive species. The contributions of coal/biomass burning and natural gas were overestimated by 2.4 and 3.9 percentage points, respectively, which were related to the emission of low-reactive species (acetylene, ethane, and propane). Based on our results, the photochemical losses of VOCs grossly affect their source apportionment and O3 formation. Thus, photochemical losses of VOCs must be thoroughly accounted to establish a precise scientific foundation for air-pollution control strategies.
引用
收藏
页数:9
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