Abstract

A regional air quality model system (RAQMS) was developed by incorporating an aqueous reaction mechanism for secondary organic aerosol (SOA) formation and primary semi-volatile (SVOC) and intermediate volatile organic compounds (IVOC) precursors to investigate various chemical pathways for SOA formation in the Beijing-Tianjin-Hebei (BTH) region in wintertime. Model comparison against observations demonstrates that the model is able to well reproduce meteorological variables and major aerosol chemical components, and the model improves SOA simulation significantly by including primary S/IVOCs (SVOC + IVOC) and aqueous reactions into the model. SVOC and IVOC emissions were relatively higher over the regions from southern Hebei province to Beijing and Tianjin, with the emission rates up to 0.15 mg m−2 hr−1 and 0.3 mg m−2 hr−1, respectively. The glyoxal (GLY) and methylglyoxal (MGLY) emissions were similar in distribution to those of S/IVOC emissions, with the maximum of 0.08 mg m −2 hr−1. The simulated SOA concentrations exhibited a southwest-northeast belt extending from southern Hebei to Beijing, with the maximum of 35 μg m−3 in southern Hebei province. The average contributions from various precursors or chemical pathways to SOA formation during the study period were estimated, in which AVOCs (anthropogenic VOCs), SVOCs, IVOCs, BVOCs (biogenic VOCs), GLY and MGLY contributed 38.4%, 24.9%, 28.4%, 0.2% and 8.1% of SOA mass concentration, respectively, in the BTH region. The maximum average contribution of GLY and MGLY to SOA reached 16% in southern Hebei province during a severe haze episode. From the clean to haze periods, concentrations of all SOA components apparently increased along with increasing atmospheric stability and weakening dispersion, but the increasing rates of SOA concentration produced by AVOCs and aqueous reactions were larger than those by primary S/IVOCs due to different chemical processes, and the AVOC-produced SOA dominated over the other SOA components during the haze periods.

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