TY - JOUR
T1 - Contrasting sources and processes of particulate species in haze days with low and high relative humidity in wintertime Beijing
AU - Huang, Ru Jin
AU - He, Yao
AU - Duan, Jing
AU - Li, Yongjie
AU - Chen, Qi
AU - Zheng, Yan
AU - Chen, Yang
AU - Hu, Weiwei
AU - Lin, Chunshui
AU - Ni, Haiyan
AU - Dai, Wenting
AU - Cao, Junji
AU - Wu, Yunfei
AU - Zhang, Renjian
AU - Xu, Wei
AU - Ovadnevaite, Jurgita
AU - Ceburnis, Darius
AU - Hoffmann, Thorsten
AU - D. ODowd, Colin
N1 - Publisher Copyright:
© Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License.
PY - 2020/7/31
Y1 - 2020/7/31
N2 - Although there are many studies of particulate matter (PM) pollution in Beijing, the sources and processes of secondary PM species during haze periods remain unclear. Limited studies have investigated the PM formation in highly polluted environments under low- and high-relative-humidity (RH) conditions. Herein, we present a systematic comparison of species in submicron particles (PM1) in wintertime Beijing (29 December 2014 to 28 February 2015) for clean periods and pollution periods under low- and high-RH conditions. PM1 species were measured with an aerosol chemical pecies monitor (ACSM) and an Aethalometer. Sources and processes for organic aerosol (OA) were resolved by positive matrix factorization (PMF) with a multilinear engine 2 (ME-2). The comparisons for clean, low-RH pollution and high-RH pollution periods are made from three different aspects, namely (a) mass concentration, (b) mass fraction and (c) growth rate in diurnal profiles. OA is the dominant component of PM1, with an average mass concentration of 56.7 ugm3 (46 ) during high-RH pollution and 67.7 ugm3 (54 ) during low-RH pollution periods. Sulfate had higher concentration and mass fraction during high-RH pollution periods, while nitrate had higher concentration and mass fraction during low-RH pollution periods. The diurnal variations of nitrate and oxygenated organic aerosol (OOA) showed a daytime increase in their concentrations during all three types of periods. Nitrate had similar growth rates during low-RH (0.40 ugm3 h1) and high-RH (0.55 ugm3 h1) pollution periods. OOA had a higher growth rate during low- RH pollution periods (1.0 ugm3 h1) than during high-RH pollution periods (0.40 ugm3 h1). In contrast, sulfate had a decreasing trend during low-RH pollution periods, while it increased significantly with a growth rate of 0.81 ugm3 h1 during high-RH pollution periods. These distinctions in mass concentrations, mass fractions and daytime growth rates may be explained by the difference in the formation processes affected by meteorological conditions. In particular, photochemical oxidation and aqueous-phase processes may both produce sulfate and nitrate. The relative importance of the two pathways, however, differs under different meteorological conditions. Additional OOA formation under high- RH (> 70 ) conditions suggests aqueous-related formation pathways. This study provides a general picture of the haze formation in Beijing under different meteorological conditions.
AB - Although there are many studies of particulate matter (PM) pollution in Beijing, the sources and processes of secondary PM species during haze periods remain unclear. Limited studies have investigated the PM formation in highly polluted environments under low- and high-relative-humidity (RH) conditions. Herein, we present a systematic comparison of species in submicron particles (PM1) in wintertime Beijing (29 December 2014 to 28 February 2015) for clean periods and pollution periods under low- and high-RH conditions. PM1 species were measured with an aerosol chemical pecies monitor (ACSM) and an Aethalometer. Sources and processes for organic aerosol (OA) were resolved by positive matrix factorization (PMF) with a multilinear engine 2 (ME-2). The comparisons for clean, low-RH pollution and high-RH pollution periods are made from three different aspects, namely (a) mass concentration, (b) mass fraction and (c) growth rate in diurnal profiles. OA is the dominant component of PM1, with an average mass concentration of 56.7 ugm3 (46 ) during high-RH pollution and 67.7 ugm3 (54 ) during low-RH pollution periods. Sulfate had higher concentration and mass fraction during high-RH pollution periods, while nitrate had higher concentration and mass fraction during low-RH pollution periods. The diurnal variations of nitrate and oxygenated organic aerosol (OOA) showed a daytime increase in their concentrations during all three types of periods. Nitrate had similar growth rates during low-RH (0.40 ugm3 h1) and high-RH (0.55 ugm3 h1) pollution periods. OOA had a higher growth rate during low- RH pollution periods (1.0 ugm3 h1) than during high-RH pollution periods (0.40 ugm3 h1). In contrast, sulfate had a decreasing trend during low-RH pollution periods, while it increased significantly with a growth rate of 0.81 ugm3 h1 during high-RH pollution periods. These distinctions in mass concentrations, mass fractions and daytime growth rates may be explained by the difference in the formation processes affected by meteorological conditions. In particular, photochemical oxidation and aqueous-phase processes may both produce sulfate and nitrate. The relative importance of the two pathways, however, differs under different meteorological conditions. Additional OOA formation under high- RH (> 70 ) conditions suggests aqueous-related formation pathways. This study provides a general picture of the haze formation in Beijing under different meteorological conditions.
UR - https://www.scopus.com/pages/publications/85089340134
U2 - 10.5194/acp-20-9101-2020
DO - 10.5194/acp-20-9101-2020
M3 - 文章
AN - SCOPUS:85089340134
SN - 1680-7316
VL - 20
SP - 9101
EP - 9114
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 14
ER -