TY - JOUR
T1 - Effects of NO2 and RH on secondary organic aerosol formation and light absorption from OH oxidation of ο-xylene
AU - Liu, Shijie
AU - Wang, Yiqian
AU - Xu, Xinbei
AU - Wang, Gehui
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/12
Y1 - 2022/12
N2 - Ο-xylene is an important aromatic volatile organic compound (VOC) in the atmosphere over urban areas. In this work, the effect of nitrogen dioxide (NO2) concentration and relative humidity (RH) on the mass concentration of secondary organic aerosols (SOA) formed from ο-xylene OH oxidization was investigated in a photooxidation chamber. The ο-xylene SOA mass concentration increased from 54.2 μg m−3 to 127.2 μg m−3 during dry conditions, but decreased from 177.7 μg m−3 to 146.5 μg m−3 during high RH conditions when the initial NO2 concentration increased form 0 ppbv to about 900 ppbv. An increase in the ratio of [NO3−]/[Org] and a decrease in the oxidation state of carbon (OSC) of SOA suggested that acid-catalyzed heterogeneous reaction was responsible for enhancing SOA formation with increasing NO2 concentrations in dry conditions. In contrast, in humid conditions, the high molecular diffusion capacity of SOA could promote the reactivity of OH towards the interior of SOA, and the enhancement of nitrous acid (HONO) formation under high NO2 conditions could promote the SOA aging processes and be responsible for the decreasing trend of SOA formation with NO2. Light absorption by SOA was also measured, and both NO2 and RH enhanced the mass absorption coefficient (MACλ = 365 nm) value for the optical properties of ο-xylene SOA. The highest MACλ = 365 nm value of ο-xylene SOA was 0.89 m2 g−1, observed during humid conditions with an initial NO2 concentration of 862 ppbv, which was 3.9 times higher than in the experiment conducted in the absence of NO2 under dry conditions. The formation of nitrogen-containing organic compounds (NOCs) and humic-like substances (HULIS) were responsible for the increased MACλ = 365 nm values of ο-xylene derived SOA. This study provides new insight into the effect of NO2 on SOA formation through the change in ο-xylene photooxidation under different RH conditions, and the complex effect of multiple environmental factors on SOA formation was also important and should not be ignored.
AB - Ο-xylene is an important aromatic volatile organic compound (VOC) in the atmosphere over urban areas. In this work, the effect of nitrogen dioxide (NO2) concentration and relative humidity (RH) on the mass concentration of secondary organic aerosols (SOA) formed from ο-xylene OH oxidization was investigated in a photooxidation chamber. The ο-xylene SOA mass concentration increased from 54.2 μg m−3 to 127.2 μg m−3 during dry conditions, but decreased from 177.7 μg m−3 to 146.5 μg m−3 during high RH conditions when the initial NO2 concentration increased form 0 ppbv to about 900 ppbv. An increase in the ratio of [NO3−]/[Org] and a decrease in the oxidation state of carbon (OSC) of SOA suggested that acid-catalyzed heterogeneous reaction was responsible for enhancing SOA formation with increasing NO2 concentrations in dry conditions. In contrast, in humid conditions, the high molecular diffusion capacity of SOA could promote the reactivity of OH towards the interior of SOA, and the enhancement of nitrous acid (HONO) formation under high NO2 conditions could promote the SOA aging processes and be responsible for the decreasing trend of SOA formation with NO2. Light absorption by SOA was also measured, and both NO2 and RH enhanced the mass absorption coefficient (MACλ = 365 nm) value for the optical properties of ο-xylene SOA. The highest MACλ = 365 nm value of ο-xylene SOA was 0.89 m2 g−1, observed during humid conditions with an initial NO2 concentration of 862 ppbv, which was 3.9 times higher than in the experiment conducted in the absence of NO2 under dry conditions. The formation of nitrogen-containing organic compounds (NOCs) and humic-like substances (HULIS) were responsible for the increased MACλ = 365 nm values of ο-xylene derived SOA. This study provides new insight into the effect of NO2 on SOA formation through the change in ο-xylene photooxidation under different RH conditions, and the complex effect of multiple environmental factors on SOA formation was also important and should not be ignored.
KW - Aerosol mass spectrometry
KW - Mass absorption coefficient
KW - Nitrogen dioxide
KW - Secondary organic aerosol
KW - ο-xylene
UR - https://www.scopus.com/pages/publications/85138394436
U2 - 10.1016/j.chemosphere.2022.136541
DO - 10.1016/j.chemosphere.2022.136541
M3 - 文章
C2 - 36150487
AN - SCOPUS:85138394436
SN - 0045-6535
VL - 308
JO - Chemosphere
JF - Chemosphere
M1 - 136541
ER -
