Spectral Light Absorption of Ambient Aerosols in Urban Beijing during Summer: An Intercomparison of Measurements from a Range of Instruments

10.4209/aaqr.2014.09.0224

Yunfei Wu1；Peng Yan；Ping Tian；Jun Tao；Ling Li；Jianmin Chen；Yangmei Zhang；Nianwen Cao；Chong Chen；Renjian Zhang

Ambient aerosol ； Black carbon ； Spectral light absorption

Aerosol and Air Quality Research

15卷4期（2015 / 08 / 01）

1178 - 1187+i-ix

英文

Aerosol light absorption is important to radiation balance, but it is difficult to accurately quantify using measurements. An intercomparison experiment for the measurement of the aerosol absorption coefficient (b_ap) was performed at an urban site in Beijing during the summer of 2012, including the filter-based particle soot absorption photometer (PSAP) and aethalometer (AE-31), and the reference photoacoustic extinctiometer (PAX), CRDS-Neph (cavity-ring down spectroscopy/nephelometer) system, and multi-angle absorption photometer (MAAP). The CRDS-Neph system and PAX performed poorly due to unexpected reasons. The corrected b_ap of the PSAP agreed well with the reference values determined by the MAAP, implying the applicability of this correction scheme as well as the credibility of the reference b_ap of the MAAP. A new conversion factor with a value of ~7.1±0.05m^2/g at ~530nm was established by regressing the reference b_ap against the AE-31 recorded black carbon (BC) concentrations, which is lower than the previously used value (8.28m^2/g).Accordingly, the absorption Ångström exponent (α_ap) was estimated as 0.85±0.21 on average. It was ~1 on clean days but significantly lower during pollution episodes, implying the main contributor to aerosol light absorption is freshlyemitted BC on clean days but aged BC during pollution. BC core sizes and the coating are likely to have a great impact on the α_ap, which needs further investigation. The mass absorption efficiency of BC was estimated by regressing the b_ap against the filter-analyzed elemental carbon (EC) concentrations, resulting in a mean of 9.2±0.5m^2/g at 670nm. It was remarkably higher during pollution episodes than on clean days, implying a high variation of aerosol properties, such as the mixing state, with pollution levels.