Sheng Fang, Jingjing Liu, Yu Chen, Fu-Ming Tao, Xuemei Duan, Jing-Yao Liu
Institute of Theoretical Chemistry, Laboratory of Theoretical and Computational Chemistry, Jilin University Changchun 130023 China
Department of Chemistry, Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education, Tsinghua University Beijing 100084 China
RSC Adv. 2018 Feb 20;8(15):7988-7996. doi: 10.1039/c8ra00411k. eCollection 2018 Feb 19.
Herein, theoretical studies were performed on the atmospheric oxidation of sulfurous acid (HSO) and sulfite ions (HSO ) by ozone (O) to produce sulfuric acid and hydrosulfate ions. The most favorable path for the HSO + O reaction has been found to be initiated from concerted H-abstraction and oxygen addition, with an overall energy barrier of 18.3 kcal mol. On the other hand, the most favorable path for the HSO + O reaction is initiated from oxygen addition, with an overall energy barrier of only 0.3 kcal mol. Kinetic simulations were performed to estimate the significance of these reactions in the formation of atmospheric sulfate and destruction of the ozone layer. The results provide new insight into the missing source of atmospheric sulfate and particulate matter.
在此,对臭氧(O)氧化亚硫酸(HSO)和亚硫酸根离子(HSO)生成硫酸和硫酸氢根离子的大气氧化过程进行了理论研究。已发现HSO + O反应最有利的路径是由协同的氢原子夺取和氧原子加成引发,总能量垒为18.3千卡/摩尔。另一方面,HSO + O反应最有利的路径是由氧原子加成引发,总能量垒仅为0.3千卡/摩尔。进行了动力学模拟以估计这些反应在大气硫酸盐形成和臭氧层破坏中的重要性。这些结果为大气硫酸盐和颗粒物缺失的来源提供了新的见解。