State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China; Hebei Collaborative Innovation Center of Coal Exploitation, Hebei University of Engineering, Handan 056038, Hebei, China.
State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China; Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, Kumamoto 862-8502, Japan.
Sci Total Environ. 2016 Nov 15;571:103-9. doi: 10.1016/j.scitotenv.2016.07.147. Epub 2016 Jul 25.
Chemical composition, morphology, size and mixture of fine particles were measured in a heavy haze and the post-haze air in Beijing in January 2012. With the occurrence of haze, the concentrations of gaseous and particulate pollutants including organics, sulfate, nitrate, and ammonium grew gradually. The hourly averaged PM2.5 concentration increased from 118μgm(-3) to 402μgm(-3) within 12h. In contrast, it was less than 10μgm(-3) in the post-haze air. Occupying approximately 46% in mass, organics were the major component of PM1 in both the haze and post-haze air. Analysis of individual particles in the size range of 0.2-1.1μm revealed that secondary-like particles and soot particles were always the majority, and most soot particles had a core-shell structure. The number ratio of secondary-like particles to soot particles in accumulation mode in the haze air was about 2:1, and that in the post-haze air was 8:1. These results indicate both secondary particle formation and primary emission contributed substantially to the haze. The mode size of the haze particles was about 0.7μm, and the mode size of the post-haze particles was 0.4μm, indicating the remarkable growth of particles in haze. However, the ratios of the core size to shell size of core-shell structure soot particles in the haze were similar to those in the post-haze air, suggesting a quick aging of soot particles in either the haze air or the post-haze air.
在 2012 年 1 月北京的重霾和霾后期间,对细颗粒物的化学组成、形态、粒径和混合情况进行了测量。随着霾的发生,气态和颗粒物污染物(包括有机物、硫酸盐、硝酸盐和铵盐)的浓度逐渐增加。在 12 小时内,PM2.5 的小时平均浓度从 118μg/m3增加到 402μg/m3。相比之下,霾后空气中 PM2.5 的浓度小于 10μg/m3。在质量上占约 46%,有机物是霾和霾后空气中 PM1 的主要成分。对 0.2-1.1μm 粒径范围内的单个粒子的分析表明,二次类似粒子和烟尘粒子始终是多数,大多数烟尘粒子具有核壳结构。在霾空气中积聚模态中二次类似粒子与烟尘粒子的数比值约为 2:1,而在霾后空气中为 8:1。这些结果表明,二次粒子形成和一次排放都对霾有重要贡献。霾颗粒的模态粒径约为 0.7μm,霾后颗粒的模态粒径约为 0.4μm,表明颗粒在霾中显著增长。然而,在霾空气或霾后空气中,核壳结构烟尘粒子的核大小与壳大小的比值相似,表明烟尘粒子在霾空气或霾后空气中快速老化。