TY - JOUR
T1 - Molecular Characterization of Oxygenated Organic Molecules and Their Dominating Roles in Particle Growth in Hong Kong
AU - Zheng, Penggang
AU - Chen, Yi
AU - Wang, Zhe
AU - Liu, Yuliang
AU - Pu, Wei
AU - Yu, Chuan
AU - Xia, Men
AU - Xu, Yang
AU - Guo, Jia
AU - Guo, Yishuo
AU - Tian, Linhui
AU - Qiao, Xiaohui
AU - Huang, Dan Dan
AU - Yan, Chao
AU - Nie, Wei
AU - Worsnop, Douglas R.
AU - Lee, Shuncheng
AU - Wang, Tao
N1 - Funding Information:
This study was supported by the Research Grants Council (RGC) of Hong Kong Special Administrative Region, China (T24-504/17-N, 16209022), the National Natural Science Foundation of China (42122062), the Hong Kong Environment and Conservation Fund (project 125/2020), and the HKUST IPO support fund for interdisciplinary research collaboration. The authors would like to acknowledge the HKPolyU University Research Facility in Chemical and Environmental Analysis (UCEA) for the equipment support and Hong Kong Environmental Protection Department for providing access to the Cape D’Aguilar Supersite AQMS and for sharing the trace gases, particles, and VOC data at the Supersite.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/5/23
Y1 - 2023/5/23
N2 - Oxygenated organic molecules (OOMs) are critical intermediates linking volatile organic compound oxidation and secondary organic aerosol (SOA) formation. Yet, the understanding of OOM components, formation mechanism, and impacts are still limited, especially for urbanized regions with a cocktail of anthropogenic emissions. Herein, ambient measurements of OOMs were conducted at a regional background site in South China in 2018. The molecular characteristics of OOMs revealed dominant nitrogen-containing products, and the influences of different factors on OOM composition and oxidation state were elucidated. Positive matrix factorization analysis resolved the complex OOM species to factors featured with fingerprint species from different oxidation pathways. A new method was developed to identify the key functional groups of OOMs, which successfully classified the majority species into carbonyls (8%), hydroperoxides (7%), nitrates (17%), peroxyl nitrates (10%), dinitrates (13%), aromatic ring-retaining species (6%), and terpenes (7%). The volatility estimation of OOMs was improved based on their identified functional groups and was used to simulate the aerosol growth process contributed by the condensation of those low-volatile OOMs. The results demonstrate the predominant role of OOMs in contributing sub-100 nm particle growth and SOA formation and highlight the importance of dinitrates and anthropogenic products from multistep oxidation.
AB - Oxygenated organic molecules (OOMs) are critical intermediates linking volatile organic compound oxidation and secondary organic aerosol (SOA) formation. Yet, the understanding of OOM components, formation mechanism, and impacts are still limited, especially for urbanized regions with a cocktail of anthropogenic emissions. Herein, ambient measurements of OOMs were conducted at a regional background site in South China in 2018. The molecular characteristics of OOMs revealed dominant nitrogen-containing products, and the influences of different factors on OOM composition and oxidation state were elucidated. Positive matrix factorization analysis resolved the complex OOM species to factors featured with fingerprint species from different oxidation pathways. A new method was developed to identify the key functional groups of OOMs, which successfully classified the majority species into carbonyls (8%), hydroperoxides (7%), nitrates (17%), peroxyl nitrates (10%), dinitrates (13%), aromatic ring-retaining species (6%), and terpenes (7%). The volatility estimation of OOMs was improved based on their identified functional groups and was used to simulate the aerosol growth process contributed by the condensation of those low-volatile OOMs. The results demonstrate the predominant role of OOMs in contributing sub-100 nm particle growth and SOA formation and highlight the importance of dinitrates and anthropogenic products from multistep oxidation.
KW - categorization scheme
KW - chemical ionization mass spectrometer (CIMS)
KW - multifunctional oxidation products
KW - nanoparticle growth
KW - oxygenated organic molecules (OOMs)
KW - positive matrix factorization (PMF)
UR - http://www.scopus.com/inward/record.url?scp=85159628990&partnerID=8YFLogxK
U2 - 10.1021/acs.est.2c09252
DO - 10.1021/acs.est.2c09252
M3 - Journal article
C2 - 37155674
AN - SCOPUS:85159628990
SN - 0013-936X
VL - 57
SP - 7764
EP - 7776
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 20
ER -