Brown carbon in atmospheric fine particles in Yangzhou, China: Light absorption properties and source apportionment

2020 ◽  
Vol 244 ◽  
pp. 105028 ◽  
Author(s):  
Yanfang Chen ◽  
Xinchun Xie ◽  
Zhan Shi ◽  
Yilin Li ◽  
Xinyu Gai ◽  
...  
2018 ◽  
Vol 187 ◽  
pp. 230-240 ◽  
Author(s):  
Yanfang Chen ◽  
Xinlei Ge ◽  
Hui Chen ◽  
Xinchun Xie ◽  
Yuntao Chen ◽  
...  

Author(s):  
Khairallah Atwi ◽  
Charles Perrie ◽  
Zezhen Cheng ◽  
Omar El Hajj ◽  
Rawad Saleh

The light-absorption properties of brown carbon (BrC) are often estimated using offline, solvent-extraction methods. However, recent studies have found evidence of insoluble species of BrC which are unaccounted for in...


2020 ◽  
Vol 261 ◽  
pp. 114239 ◽  
Author(s):  
Pengfei Chen ◽  
Shichang Kang ◽  
Lekhendra Tripathee ◽  
Kirpa Ram ◽  
Maheswar Rupakheti ◽  
...  

2018 ◽  
Vol 625 ◽  
pp. 246-251 ◽  
Author(s):  
Chong-Shu Zhu ◽  
Jun-Ji Cao ◽  
Ru-Jin Huang ◽  
Zhen-Xing Shen ◽  
Qi-Yuan Wang ◽  
...  

2020 ◽  
Vol 54 (7) ◽  
pp. 849-863 ◽  
Author(s):  
Zezhen Cheng ◽  
Khairallah M. Atwi ◽  
Zhenhong Yu ◽  
Anita Avery ◽  
Edward C. Fortner ◽  
...  

2020 ◽  
Author(s):  
Ru-Jin Huang ◽  
Wei Yuan ◽  
Lu Yang ◽  
Jie Guo ◽  
Jing Duan ◽  
...  

<p>The impact of brown carbon aerosol (BrC) on the Earth’s radiative forcing balance has been widely recognized but remains uncertain, mainly because the relationships among BrC sources, chromophores, and optical properties of aerosol are poorly understood (Feng et al., 2013; Laskin et al., 2015). In this work, the light absorption properties and chromophore composition of BrC were investigated for samples collected in Xi’an, Northwest China from 2015 to 2016. Both absorption Ångström exponent and mass absorption efficiency show distinct seasonal differences, which could be attributed to the differences in sources and chromophore composition of BrC. Three groups of light-absorbing organics were found to be important BrC chromophores, including those show multiple absorption peaks at wavelength > 350 nm (12 polycyclic aromatic hydrocarbons and their derivatives) and those show single absorption peak at wavelength < 350 nm (10 nitrophenols and nitrosalicylic acids and 3 methoxyphenols). These measured BrC chromophores show distinct seasonal differences and contribute on average about 1.1% and 3.3% of light absorption of methanol-soluble BrC at 365 nm in summer and winter, respectively, about 7 and 5 times higher than the corresponding mass fractions in total organic carbon. The sources of BrC were resolved by positive matrix factorization (PMF) using these chromophores instead of commonly used non-light absorbing organic markers as model inputs. Our results show that in spring vehicular emissions and secondary formation are major sources of BrC (~70%), in fall coal combustion and vehicular emissions are major sources (~70%), in winter biomass burning and coal combustion become major sources (~80%), while in summer secondary BrC dominates (~60%).</p><p> </p><p>References:</p><p>Feng, Y., V. Ramanathan, and V. R. Kotamarthi: Brown carbon: A significant atmospheric absorber of solar radiation?, Atmos. Chem. Phys., 13, 8607-8621, doi:10.5194/acp-13-8607-2013, 2013.</p><p>Laskin, A., J. Laskin, and S. A. Nizkorodov: Chemistry of atmospheric brown carbon, Chem. Rev., 115, 4335-4382, doi:10.1021/cr5006167, 2015.</p>


2013 ◽  
Vol 13 (7) ◽  
pp. 18233-18276 ◽  
Author(s):  
J. Liu ◽  
M. Bergin ◽  
H. Guo ◽  
L. King ◽  
N. Kotra ◽  
...  

Abstract. Light absorbing organic carbon, often termed brown carbon, has the potential to significantly contribute to the visible light absorption budget, particularly at shorter wavelengths. Currently, the relative contributions of particulate brown carbon to light absorption, as well as the sources of brown carbon are poorly understood. With this in mind field measurements were made at both urban (Atlanta), and rural (Yorkville) sites in Georgia. Measurements in Atlanta were made at both a central site and a road side site adjacent to a main highway near the city center. Fine particle brown carbon optical absorption is estimated based on Mie calculations using direct size resolved measurements of chromophores in filter extracts. Size-resolved atmospheric aerosol samples were collected using a cascade impactor and analyzed for water-soluble organic carbon (WSOC), organic and elemental carbon (OC and EC), and solution light absorption spectra of water and methanol extracts. Methanol extracts were more light-absorbing than water extracts for all size ranges and wavelengths. Absorption refractive indices of the organic extracts were calculated from solution measurements for a range of wavelengths and used with Mie theory to predict the light absorption by fine particles comprised of these components, under the assumption that brown carbon and other aerosol components were externally mixed. For all three sites, chromophores were predominately in the accumulation mode with an aerodynamic mean diameter of 0.5 μm, an optically effective size range resulting in predicted particle light absorption being a factor of 2 higher than bulk solution absorption. Fine particle absorption was also measured with a Multi-Angle Absorption Photometer (MAAP) and seven-wavelength Aethalometer. Scattering-corrected aethalometer and MAAP absorption were in good agreement at 670 nm and Mie-estimated absorption based on size-resolved EC data were within 30% of these optical instruments. When applied to solution measurements, at all sites, Mie-predicted brown carbon absorption at 350 nm contributed a significant fraction (20 to 40%) relative to total light absorption, with highest contributions at the rural site where organic to elemental carbon ratios were highest. Brown carbon absorption, however, was highest by the roadside site due to vehicle emissions. The multi-wavelength aethalometer did not detect brown carbon, having an absorption Ångstrom exponent near one. Although the results are within the estimated Aethalometer uncertainties, the direct measurement of brown carbon in solution definitively shows that it is present and this Mie analysis suggests it is optically important in the near UV range in both a rural and urban environment during summer when biomass burning emissions are low.


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