中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Spatial characterization of HCHO and reapportionment of its secondary sources considering photochemical loss in Taiyuan, China

文献类型:期刊论文

作者Hua, Jingya2; Cui, Yang2; Guo, Lili2; Li, Hongyan2; Fan, Jie2; Li, Yanan2; Wang, Yonghong3; Liu, Kankan1; He, Qiusheng2; Wang, Xinming4
刊名SCIENCE OF THE TOTAL ENVIRONMENT
出版日期2023-03-20
卷号865页码:14
关键词Formaldehyde Spatial distribution Photochemical loss Source apportionment
ISSN号0048-9697
DOI10.1016/j.scitotenv.2022.161069
英文摘要Formaldehyde (HCHO) plays an important role in atmospheric ozone (O3) formation. To accurately identify the sources of HCHO, carbonyls and volatile organic compounds (VOCs) were measured at three urban sites (Taoyuan, TY-U; Jinyuan, JY-U; Xiaodian, XD-U) and a suburban site (Shanglan, SL-B) in Taiyuan during a high O3 period (from July 20 to August 3, 2020). The average mixing ratio of HCHO at XD-U (8.1 +/- 2.8 ppbv) was comparable to those at TY-U (7.4 +/- 2.1 ppbv) and JY-U (7.0 +/- 2.3 ppbv) but higher (p < 0.01) than that at SL-B (4.9 +/- 2.3 ppbv). HCHO contributed to 54.3-59.9 % of the total ozone formation potentials (OFPs) of non-methane hydrocarbons (NMHCs) at four sites. The diurnal variation of HCHO concentrations reached a peak value at 12:00-15:00, which may be attributed to the strong photochemical reaction. To obtain more accurate source results of HCHO under the condition of photochemical loss, the initial concentrations of NMHCs were estimated based on photochemical age parameterization and incorporated into the positive matrix factorization (PMF) model (termed IC-PMF). According to the ICPMF results, secondary formation (SF) contributed the most to HCHO at XD-U (35.6 %) and SL-B (25.1 %), whereas solvent usage (SU) (40.9 %) and coking sources (CS) (36.0 %) were the major sources at TY-U and JY-U, respectively. Compared to the IC-PMF, the conventional PMF analysis based on the observed data underestimated the contributions of SU (100.5-154.2 %) and biogenic sources (BS) (28.5-324.7 %). Further reapportionment of secondary HCHO by multiple linear regression indicated that SU dominated the sources of HCHO at SL-B (28.3 %) and TY-U (41.7 %), while industrial emissions (IE) and CS contributed the most to XD-U (26.6 %) and JY-U (43.0 %) in Taiyuan from north to south, respectively.
WOS研究方向Environmental Sciences & Ecology
语种英语
WOS记录号WOS:000918639300001
源URL[http://ir.gig.ac.cn/handle/344008/72436]  
专题有机地球化学国家重点实验室
通讯作者Cui, Yang; Wang, Yonghong
作者单位1.North Univ China, Sch Environm & Safety Engn, Taiyuan 030051, Peoples R China
2.Taiyuan Univ Sci & Technol, Sch Environm & Resources, Taiyuan 030024, Peoples R China
3.Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100085, Peoples R China
4.Chinese Acad Sci, Guangzhou Inst Geochem, State Key Lab Organ Geochem, Guangzhou 510640, Peoples R China
推荐引用方式
GB/T 7714
Hua, Jingya,Cui, Yang,Guo, Lili,et al. Spatial characterization of HCHO and reapportionment of its secondary sources considering photochemical loss in Taiyuan, China[J]. SCIENCE OF THE TOTAL ENVIRONMENT,2023,865:14.
APA Hua, Jingya.,Cui, Yang.,Guo, Lili.,Li, Hongyan.,Fan, Jie.,...&Wang, Xinming.(2023).Spatial characterization of HCHO and reapportionment of its secondary sources considering photochemical loss in Taiyuan, China.SCIENCE OF THE TOTAL ENVIRONMENT,865,14.
MLA Hua, Jingya,et al."Spatial characterization of HCHO and reapportionment of its secondary sources considering photochemical loss in Taiyuan, China".SCIENCE OF THE TOTAL ENVIRONMENT 865(2023):14.

入库方式: OAI收割

来源:广州地球化学研究所

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