TY - JOUR
T1 - Characteristics and source apportionment of water-soluble organic nitrogen (WSON) in PM2.5 in Hong Kong
T2 - With focus on amines, urea, and nitroaromatic compounds
AU - Leung, Chin Wai
AU - Wang, Xuemei
AU - Hu, Di
N1 - This work was supported by the National Natural Science Foundation of China (21976151) and the General Research Fund of Hong Kong Research Grants Council (12201220 and 12304215). The authors thank the Environmental Central Facility (ENVF) at Hong Kong University of Science and Technology (HKUST) for real-time environmental and air quality data (http://envf.ust.hk/dataview/gts/current/).
Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/5/5
Y1 - 2024/5/5
N2 - Water-soluble organic nitrogen (WSON) is ubiquitous in fine particulate matter (PM2.5) and poses health and environmental risks. However, there is limited knowledge regarding its comprehensive speciation and source-specific contributions. Here, we conducted chemical characterization and source apportionment of WSON in 65 PM2.5 samples collected in Hong Kong during a 1-yr period. Using various mass-spectrometry-based techniques, we quantified 22 nitrogen-containing organic compounds (NOCs), including 17 nitroaromatics (NACs), four amines, and urea. The most abundant amine and NACs were dimethylamine and 4-nitrocatechol, respectively. Two secondary (i.e., secondary formation and secondary nitrate) and five primary sources (i.e., sea salt, fugitive dust, marine vessels, vehicle exhaust, and biomass burning) of WSON and these three categories of NOCs were identified. Throughout the year, secondary sources dominated WSON formation (69.0%), while primary emissions had significant contributions to NACs (77.1%), amines (75.9%), and urea (83.7%). Fugitive dust was the leading source of amines and urea, while biomass burning was the main source of NACs. Our multi-linear regression analysis revealed the significant role of sulfate, NO3, nitrate, liquid water content, and particle pH on WSON formation, highlighting the importance of nighttime NO3 processing and heterogeneous and aqueous-phase formation of NOCs in the Hong Kong atmosphere.
AB - Water-soluble organic nitrogen (WSON) is ubiquitous in fine particulate matter (PM2.5) and poses health and environmental risks. However, there is limited knowledge regarding its comprehensive speciation and source-specific contributions. Here, we conducted chemical characterization and source apportionment of WSON in 65 PM2.5 samples collected in Hong Kong during a 1-yr period. Using various mass-spectrometry-based techniques, we quantified 22 nitrogen-containing organic compounds (NOCs), including 17 nitroaromatics (NACs), four amines, and urea. The most abundant amine and NACs were dimethylamine and 4-nitrocatechol, respectively. Two secondary (i.e., secondary formation and secondary nitrate) and five primary sources (i.e., sea salt, fugitive dust, marine vessels, vehicle exhaust, and biomass burning) of WSON and these three categories of NOCs were identified. Throughout the year, secondary sources dominated WSON formation (69.0%), while primary emissions had significant contributions to NACs (77.1%), amines (75.9%), and urea (83.7%). Fugitive dust was the leading source of amines and urea, while biomass burning was the main source of NACs. Our multi-linear regression analysis revealed the significant role of sulfate, NO3, nitrate, liquid water content, and particle pH on WSON formation, highlighting the importance of nighttime NO3 processing and heterogeneous and aqueous-phase formation of NOCs in the Hong Kong atmosphere.
KW - Amines
KW - Nitroaromatic compounds
KW - PM2.5
KW - Urea
KW - Water-soluble organic nitrogen (WSON)
UR - http://www.scopus.com/inward/record.url?scp=85186627500&partnerID=8YFLogxK
U2 - 10.1016/j.jhazmat.2024.133899
DO - 10.1016/j.jhazmat.2024.133899
M3 - Journal article
C2 - 38430595
AN - SCOPUS:85186627500
SN - 0304-3894
VL - 469
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 133899
ER -