Back to Search Start Over

Water-Insoluble Organics Dominate Brown Carbon in Wintertime Urban Aerosol of China: Chemical Characteristics and Optical Properties.

Authors :
Huang RJ
Yang L
Shen J
Yuan W
Gong Y
Guo J
Cao W
Duan J
Ni H
Zhu C
Dai W
Li Y
Chen Y
Chen Q
Wu Y
Zhang R
Dusek U
O'Dowd C
Hoffmann T
Source :
Environmental science & technology [Environ Sci Technol] 2020 Jul 07; Vol. 54 (13), pp. 7836-7847. Date of Electronic Publication: 2020 Jun 18.
Publication Year :
2020

Abstract

The chromophores responsible for light absorption in atmospheric brown carbon (BrC) are not well characterized, which hinders our understanding of BrC chemistry, the links with optical properties, and accurate model representations of BrC to global climate and atmospheric oxidative capacity. In this study, the light absorption properties and chromophore composition of three BrC fractions of different polarities were characterized for urban aerosol collected in Xi'an and Beijing in winter 2013-2014. These three BrC fractions show large differences in light absorption and chromophore composition, but the chromophores responsible for light absorption are similar in Xi'an and Beijing. Water-insoluble BrC (WI-BrC) fraction dominates the total BrC absorption at 365 nm in both Xi'an (51 ± 5%) and Beijing (62 ± 13%), followed by a humic-like fraction (HULIS-BrC) and high-polarity water-soluble BrC. The major chromophores identified in HULIS-BrC are nitrophenols and carbonyl oxygenated polycyclic aromatic hydrocarbons (OPAHs) with 2-3 aromatic rings (in total 18 species), accounting for 10% and 14% of the light absorption of HULIS-BrC at 365 nm in Xi'an and Beijing, respectively. In comparison, the major chromophores identified in WI-BrC are PAHs and OPAHs with 4-6 aromatic rings (in total 16 species), contributing 6% and 8% of the light absorption of WI-BrC at 365 nm in Xi'an and Beijing, respectively.

Details

Language :
English
ISSN :
1520-5851
Volume :
54
Issue :
13
Database :
MEDLINE
Journal :
Environmental science & technology
Publication Type :
Academic Journal
Accession number :
32479722
Full Text :
https://doi.org/10.1021/acs.est.0c01149