Journal
SCIENCE OF THE TOTAL ENVIRONMENT
Volume 770, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.scitotenv.2020.144821
Keywords
Black carbon; Absorption enhancement; Brown carbon; North China Plain; Coal combustion
Categories
Funding
- National Key Research and Development Program of China [2017YFC0212704]
- National Natural Science Foundation of China [91744207]
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This study investigated the light absorption enhancement of black carbon due to coated materials in urban and rural areas of North China Plain in winter 2019, finding that the rural site had slightly higher average E-abs compared to the urban site. The dependence of E-abs on coating materials was limited, but showed significant increases at lower relative humidity levels.
The light absorption black carbon (BC) and brown carbon (BrC) are two important sources of uncertainties in radiative forcing estimate. Here we investigated the light absorption enhancement (E-abs) of BC due to coated materials at an urban (Beijing) and a rural site (Gucheng) in North China Plain (NCP) in winter 2019 by using a photoacoustic extinctiometer coupled with a thermodenuder. Our results showed that the average (+/- 1s) E-abs was 1.32 (+/- 0.15) at the rural site, which was slightly higher than that at the urban site (1.24 +/- 0.15). The dependence of E-abs on coating materials was found to be relatively limited at both sites. However, E-abs presented considerable increases as a function of relative humidity below 70%. Further analysis showed that E-abs during non-heating period in Beijing was mainly caused by secondary components, while it was dominantly contributed by enhanced primary emissions in heating season at both sites. In particular, aerosol particles mixed with coal combustion emissions had a large impact on E-abs (>1.40), while the fresh traffic emissions and freshly oxidized secondary OA (SOA) had limited E-abs (1.00-1.23). Although highly aged or aqueous-phase processed SOA coated on BC showed the largest E-abs, their contributions to the bulk absorption enhancement were generally small. We also quantified the absorption of BrC and source contributions. The results showed the BrC absorption at the rural site was nearly twice that of urban site, yet absorption Angstrom exponents were similar. Multiple linear regression analysis highlighted the major sources of BrC being coal combustion emissions and photochemical SOA at both sites with additional biomass burning at the rural site. Overall, our results demonstrated the relatively limited winter light absorption enhancement of BC in different chemical environments in NCP, which needs be considered in regional climate models to improve BC radiative forcing estimates. (C) 2021 Elsevier B.V. All rights reserved.
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