TY - JOUR
T1 - Single particle diversity and mixing state of carbonaceous aerosols in Guangzhou, China
AU - Cheng, Chunlei
AU - Chan, Chak K.
AU - Lee, Berto Paul
AU - Gen, Masao
AU - Li, Mei
AU - Yang, Suxia
AU - Hao, Feng
AU - Wu, Cheng
AU - Cheng, Peng
AU - Wu, Dui
AU - Li, Lei
AU - Huang, Zhengxu
AU - Gao, Wei
AU - Fu, Zhong
AU - Zhou, Zhen
N1 - Generated from Scopus record by KAUST IRTS on 2023-07-06
PY - 2021/2/1
Y1 - 2021/2/1
N2 - Many field studies have investigated the formation mechanisms of organic aerosol (OA) based on bulk analysis, yet the source and formation process of individual organic particles may be quite different due to the diversity of chemical composition and mixing state in single particles. Here we present the observation results of chemical composition and mixing state of carbonaceous single particles at an urban site in Guangzhou. The carbonaceous particles accounted for 74.6% of the total detected single particles, and were grouped into four types including elemental carbon-aged (EC-aged), elemental and organic carbon (ECOC), organic carbon-rich (OC-rich) and secondary ions-rich (SEC) particles. The formation of EC-aged particles was closely associated with the absorption of organics onto fresh EC particles from primary sources, and the further enrichment of organics in EC-aged particles resulted in the production of ECOC particles. In the daytime OC-rich and SEC particles were mainly produced from the photochemical reactions, while in the nighttime their sharp increases were found along with the enrichment of nitrate and organic nitrogen fragments, suggesting the heterogeneous formation of nitrate and organic nitrogen in OC-rich and SEC particles. The production rates of carbonaceous particles were also investigated in an episodic event, and the EC-aged particles showed the highest production rate compared to the other carbonaceous particles both in the daytime and nighttime, suggesting a significant role of EC in the formation and aging process of carbonaceous particles. The results from this work have revealed different formation processes and production rates of carbonaceous particles due to their diversity in mixing state, providing further insights into the formation mechanisms of OA in field studies.
AB - Many field studies have investigated the formation mechanisms of organic aerosol (OA) based on bulk analysis, yet the source and formation process of individual organic particles may be quite different due to the diversity of chemical composition and mixing state in single particles. Here we present the observation results of chemical composition and mixing state of carbonaceous single particles at an urban site in Guangzhou. The carbonaceous particles accounted for 74.6% of the total detected single particles, and were grouped into four types including elemental carbon-aged (EC-aged), elemental and organic carbon (ECOC), organic carbon-rich (OC-rich) and secondary ions-rich (SEC) particles. The formation of EC-aged particles was closely associated with the absorption of organics onto fresh EC particles from primary sources, and the further enrichment of organics in EC-aged particles resulted in the production of ECOC particles. In the daytime OC-rich and SEC particles were mainly produced from the photochemical reactions, while in the nighttime their sharp increases were found along with the enrichment of nitrate and organic nitrogen fragments, suggesting the heterogeneous formation of nitrate and organic nitrogen in OC-rich and SEC particles. The production rates of carbonaceous particles were also investigated in an episodic event, and the EC-aged particles showed the highest production rate compared to the other carbonaceous particles both in the daytime and nighttime, suggesting a significant role of EC in the formation and aging process of carbonaceous particles. The results from this work have revealed different formation processes and production rates of carbonaceous particles due to their diversity in mixing state, providing further insights into the formation mechanisms of OA in field studies.
UR - https://linkinghub.elsevier.com/retrieve/pii/S0048969720357119
UR - http://www.scopus.com/inward/record.url?scp=85090577856&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2020.142182
DO - 10.1016/j.scitotenv.2020.142182
M3 - Article
SN - 1879-1026
VL - 754
JO - Science of the Total Environment
JF - Science of the Total Environment
ER -