Measurement report: Evaluation of sources and mixing state of black carbon aerosol under the background of emission reduction in the North China Plain: implications for radiative effect

Abstract. Accurate understanding of sources and mixing state of black carbon (BC) aerosol is essential for assessing its impacts on air quality and climatic effect. Here, a winter campaign (December 2017–January 2018) was conducted in the North China Plain (NCP) to evaluate the sources, coating composition, and radiative effect of BC under the background of emission reduction since 2013. Results show that liquid fossil fuel source (i.e., traffic emission) and solid fuel source (i.e., biomass and coal burning) contributed 69 % and 31 % to the total BC mass, respectively, using a multiwavelength optical approach combined with the source-based aerosol absorption Ångström exponent values. The air quality model indicates that local emission was the dominant contributor to BC at the measurement site on average, however, emissions in the NCP exerted a critical role for high BC episode. Six classes of BC-containing particles were identified, including (1) BC coated by organic carbon and sulphate (52 % of total BC-containing particles), (2) BC coated by Na and K (24 %), (3) BC coated by K, sulphate, and nitrate (17 %), (4) BC associated with biomass burning (6 %), (5) Pure-BC (1 %), and (6) others (1 %). Different BC sources had distinct impacts on those BC-containing particles. A radiative transfer model estimated that the amount of BC detected can produce an atmospheric forcing of +18.0 W m−2 and a heating rate of 0.5 K day−1. Results presented herein highlight that further reduction of solid fuel combustion-related BC may be a more effective way to mitigate regional warming in the NCP, although larger BC contribution was from liquid fossil fuel source.