资源环境科技发展态势分析平台

The effects of aerosols on visibility through scattering and absorption of light and on climate through altering cloud droplet concentration are closely associated with their hygroscopic properties. Here, based on field campaigns in winter and summer in Beijing, we compare the size-resolved hygroscopic parameter (kappa(gf)) of ambient fine particles derived by an HTDMA (hygroscopic tandem differential mobility analyzer) to that (denoted as kappa(chem)) calculated by an HR-ToF-AMS (high-resolution time-of-flight aerosol mass spectrometer) measurements using a simple rule with the hypothesis of uniform internal mixing of aerosol particles. We mainly focus on contrasting the disparity of kappa(gf) and kappa(chem) between summer and winter to reveal the impact of atmospheric processes/emission sources on aerosol hygroscopicity and to evaluate the uncertainty in estimating particle hygroscopicity with the hypothesis. We show that, in summer, the kappa(chem) for 110, 150, and 200 nm particles was on average similar to 10 %-12% lower than kappa(gf), with the greatest difference between the values observed around noontime when aerosols experience rapid photochemical aging. In winter, no apparent disparity between kappa(chem) and kappa(gf) is observed for those > 100 nm particles around noontime, but the kappa(chem) is much higher than kappa(gf) in the late afternoon when ambient aerosols are greatly influenced by local traffic and cooking sources. By comparing with the observation from the other two sites (Xingtai, Hebei and Xinzhou, Shanxi) of north China, we verify that atmospheric photochemical aging of aerosols enhances their hygroscopicity and leads to 10 %-20% underestimation in kappa(chem) if using the uniform internal mixing assumption. The effect is found more significant for these > 100 nm particles observed in remote or clean regions. The lower kappa(chem) likely resulted from multiple impacts of inappropriate application of the density and hygroscopic parameter of organic aerosols in the calculation, as well as influences from chemical interaction between organic and inorganic compounds on the overall hygroscopicity of mixed particles. We also find that local/regional primary emissions, which result in a large number of externally mixed BC (black carbon) and POA (primary organic aerosol) in urban Beijing during traffic rush hour time, cause a 20 %-40% overestimation of the hygroscopic parameter. This is largely due to an inappropriate use of density of the BC particles that is closely associated with its morphology or the degree of its aging. The results show that the calculation can be improved by applying an effective density of fresh BC (0.25-0.45 g cm(-3)) in the mixing rule assumption. Our study suggests that it is critical to measure the effective density and morphology of ambient BC, in particular in those regions with influences of rapid secondary conversion/aging processes and local sources, so as to accurately parameterize the effect of BC aging on particle hygroscopicity.