Particle acidity and sulfate production during severe haze events in China cannot be reliably inferred by assuming a mixture of inorganic salts

Gehui Wang(Chinese Academy of Sciences), Fang Zhang(Beijing Normal University), Jianfei Peng(Peking University), Lian Duan(East China University of Science and Technology), Yuemeng Ji(Guangdong University of Technology), Wilmarie Marrero-Ortiz(Texas A&M University), Jiayuan Wang(Chinese Academy of Sciences), Jianjun Li(Chinese Academy of Sciences), Can Wu(Chinese Academy of Sciences), Cong Cao(Chinese Academy of Sciences), Yuan Wang(Jet Propulsion Laboratory), Jun Zheng(Nanjing University of Information Science and Technology), Jeremiah Secrest(Texas A&M University), Yixin Li(Texas A&M University), Yuying Wang(Jet Propulsion Laboratory), Hong Li(Chinese Research Academy of Environmental Sciences), Na Li(Jilin Jianzhu University), Renyi Zhang(Peking University)
Atmospheric chemistry and physics
July 17, 2018
Cited by 124Open Access
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Abstract

Abstract. Atmospheric measurements showed rapid sulfate formation during severe haze episodes in China, with fine particulate matter (PM) consisting of a multi-component mixture that is dominated by organic species. Several recent studies using the thermodynamic model estimated the particle acidity and sulfate production rate, by treating the PM exclusively as a mixture of inorganic salts dominated by ammonium sulfate and neglecting the effects of organic compounds. Noticeably, the estimated pH and sulfate formation rate during pollution periods in China were highly conflicting among the previous studies. Here we show that a particle mixture of inorganic salts adopted by the previous studies does not represent a suitable model system and that the acidity and sulfate formation cannot be reliably inferred without accounting for the effects of multi-aerosol compositions during severe haze events in China. Our laboratory experiments show that SO2 oxidation by NO2 with NH3 neutralization on fine aerosols is dependent on the particle hygroscopicity, phase-state, and acidity. Ammonium sulfate and oxalic acid seed particles exposed to vapors of SO2, NO2, and NH3 at high relative humidity (RH) exhibit distinct size growth and sulfate formation. Aqueous ammonium sulfate particles exhibit little sulfate production, in contrast to aqueous oxalic acid particles with significant sulfate production. Our field measurements demonstrate significant contribution of water-soluble organic matter to fine PM in China and indicate that the use of oxalic acid in laboratory experiments is representative of ambient organic dominant aerosols. While the particle acidity cannot be accurately determined from field measurements or calculated using the thermodynamic model, our results reveal that the pH value of ambient organics-dominated aerosols is sufficiently high to promote efficient SO2 oxidation by NO2 with NH3 neutralization under polluted conditions in China.


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