scholarly journals Supplementary material to "Measurement Report: Size distributions of inorganic and organic components in particulate matter from a megacity in northern China: dependence upon seasons and pollution levels"

Author(s):  
Yingze Tian ◽  
Yinchang Feng ◽  
Yongli Liang ◽  
Yixuan Li ◽  
Qianqian Xue ◽  
...  
2020 ◽  
Author(s):  
Yingze Tian ◽  
Yinchang Feng ◽  
Yongli Liang ◽  
Yixuan Li ◽  
Qianqian Xue ◽  
...  

Abstract. Size distributions of inorganic and organic components in particulate matter (PM) provide critical information on its sources, fate and pollution processes. Here, ions, elements, carbon fractions, n-alkanes, polycyclic aromatic hydrocarbons (PAHs), hopanes and steranes in size-resolved (9 stages) PM were analyzed during one year in a typical northern Chinese industrial megacity (Tianjin). We found that the concentrations of organic carbon fraction OC3, NO3− (or SO42−) and the sum of crustal elements were the highest in the pseudo-ultrafine ( 2.1 μm) modes, respectively. The diagnostic ratios of organic components consistently suggest that the traffic influence was stronger during summer and coal combustion during winter. Nitrate and high molecular weight PAHs were concentrated in the fine mode during winter, while nitrate and low molecular weight PAHs showed bimodal distributions especially during summer due to repartitioning. Long-chain n-alkanes showed a peak in the coarse mode during spring and summer, indicating a relatively stronger vegetation source and resuspended dust. Furthermore, we found a major difference in the size distribution of aerosol components during heavy pollution episodes (PM10 > 233 μg m−3) in different seasons: in spring, OC fractions, 4- and 5-ring PAHs, hopanes and C18–C33 n-alkanes were enhanced at 1.1–3.3 μm, implying that they may arise from local combustion sources which emit relatively large particles; in summer PM mass, SO42−, NH4+, Al, and C26–C33 n-alkanes were enhanced mainly in the coarse mode, peaking at 5.8–9.0 μm, indicating a large contribution from resuspended dust or heterogeneous reactions on dusts; in the winter and autumn, NO3− was significantly enhanced followed by SO42−, NH4+, OC and EC with their peaks shifting from 0.43–0.65 μm to 0.65–2.1 μm, indicating strong atmospheric processing. These results reveal that the size distributions of inorganic and organic aerosol components are dependent on the seasons and pollution levels as a result of the differing sources and physicochemical processes.


2021 ◽  
Author(s):  
Ülkü Alver Şahin ◽  
Roy M. Harrison ◽  
Mohammed S. Alam ◽  
David C. S. Beddows ◽  
Dimitrios Bousiotis ◽  
...  

2004 ◽  
Vol 38 (20) ◽  
pp. 3127-3141 ◽  
Author(s):  
Juan C. Cabada ◽  
Sarah Rees ◽  
Satoshi Takahama ◽  
Andrey Khlystov ◽  
Spyros N. Pandis ◽  
...  

2006 ◽  
Vol 85 (1) ◽  
pp. 110-132 ◽  
Author(s):  
Finn Brudevold ◽  
Luville T. Steadman ◽  
Frank A. Smith

2012 ◽  
Vol 55 ◽  
pp. 525-532 ◽  
Author(s):  
Yungang Wang ◽  
Philip K. Hopke ◽  
Xiaoyan Xia ◽  
Oliver V. Rattigan ◽  
David C. Chalupa ◽  
...  

2011 ◽  
Vol 11 (16) ◽  
pp. 8809-8823 ◽  
Author(s):  
N. Hiranuma ◽  
S. D. Brooks ◽  
J. Gramann ◽  
B. W. Auvermann

Abstract. Housing roughly 10 million head of cattle in the United States alone, open air cattle feedlots represent a significant but poorly constrained source of atmospheric particles. Here we present a comprehensive characterization of physical and chemical properties of particles emitted from a large representative cattle feedlot in the Southwest United States. In the summer of 2008, measurements and samplings were conducted at the upwind and downwind edges of the facility. A series of far-field measurements and samplings was also conducted 3.5 km north of the facility. Two instruments, a GRIMM Sequential Mobility Particle Sizer (SMPS) and a GRIMM Portable Aerosol Spectrometer (PAS), were used to measure particle size distributions over the range of 0.01 to 25 μm diameter. Raman microspectroscopy was used to determine the chemical composition of particles on a single particle basis. Volume size distributions of dust were dominated by coarse mode particles. Twenty-four hour averaged concentrations of PM10 (particulate matter with a diameter of 10 μm or less) were as high as 1200 μg m−3 during the campaign. The primary constituents of the particulate matter were carbonaceous materials, such as humic acid, water soluble organics, and less soluble fatty acids, including stearic acid and tristearin. A significant fraction of the organic particles was present in internal mixtures with salts. Basic characteristics such as size distribution and composition of agricultural aerosols were found to be different than the properties of those found in urban and semi-urban aerosols. Failing to account for such differences may lead to errors in estimates of aerosol effects on local air quality, visibility, and public health.


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