Self-Catalytic Reaction of SO3 and NH3 To Produce Sulfamic Acid and Its Implication to Atmospheric Particle Formation
Author(s) -
Hao Li,
Jie Zhong,
Hanna Vehkamäki,
Theo Kurtén,
Weigang Wang,
Maofa Ge,
Shaowen Zhang,
ZeSheng Li,
Xiuhui Zhang,
Joseph S. Francisco,
Xiao Cheng Zeng
Publication year - 2018
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b04928
Subject(s) - sulfamic acid , chemistry , catalysis , particle (ecology) , inorganic chemistry , organic chemistry , geology , oceanography
Sulfur trioxide (SO 3 ) is one of the most active chemical species in the atmosphere, and its atmospheric fate has profound implications to air quality and human health. The dominant gas-phase loss pathway for SO 3 is generally believed to be the reaction with water molecules, resulting in sulfuric acid. The latter is viewed as a critical component in the new particle formation (NPF). Herein, a new and competitive loss pathway for SO 3 in the presence of abundant gas-phase ammonia (NH 3 ) species is identified. Specifically, the reaction between SO 3 and NH 3 , which produces sulfamic acid, can be self-catalyzed by the reactant (NH 3 ). In dry and heavily polluted areas with relatively high concentrations of NH 3 , the effective rate constant for the bimolecular SO 3 -NH 3 reaction can be sufficiently fast through this new loss pathway for SO 3 o become competitive with the conventional loss pathway for SO 3 with water. Furthermore, this study shows that the final product of the reaction, namely, sulfamic acid, can enhance the fastest possible rate of NPF from sulfuric acid and dimethylamine (DMA) by about a factor of 2. An alternative source of stabilizer for acid-base clustering in the atmosphere is suggested, and this new mechanism for NPF has potential to improve atmospheric modeling in highly polluted regions.
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