Chemical Production of Oxygenated Volatile Organic Compounds Strongly Enhances Boundary-Layer Oxidation Chemistry and Ozone Production
Hang Qu, Yuhang Wang, Ruixiong Zhang, Xiaoxi Liu, L. G. Huey, Steven Sjostedt, Limin Zeng, Keding Lu, Yusheng Wu, Min Shao, Min Hu, Zhaofeng Tan, Hendrik Fuchs, Sebastian Broch, Andreas Wahner, Tong Zhu, Yuanhang Zhang
Abstract
Photolysis of oxygenated volatile organic compounds (OVOCs) produces a primary source of free radicals, including OH and inorganic and organic peroxy radicals (HO 2 and RO 2 ), consequently increasing photochemical ozone production. The amplification of radical cycling through OVOC photolysis provides an important positive feedback mechanism to accelerate ozone production. The large production of OVOCs near the surface helps promote photochemistry in the whole boundary layer. This amplifier effect is most significant in regions with high nitrogen oxides (NO x ) and VOC concentrations such as Wangdu, China. Using a 1-D model with comprehensive observations at Wangdu and the Master Chemical Mechanism (MCM), we find that OVOC photolysis is the largest free-radical source in the boundary layer (46%). The condensed chemistry mechanism we used severely underestimates the OVOC amplifier effect in the boundary layer, resulting in a lower ozone production rate sensitivity to NO x emissions. Due to this underestimation, the model-simulated threshold NO x emission value, below which ozone production decreases with NO x emission decrease, is biased low by 24%. The underestimated OVOC amplifier effect in a condensed mechanism implies a low bias in the current 3-D model-estimated efficacy of NO x emission reduction on controlling ozone in polluted urban and suburban regions of China.