期刊文献+

Theoretical Study on Impact of Single Water Molecule on OH+O3 Reaction

单个水分子影响OH+O3反应的理论研究
下载PDF
导出
摘要 Quantum chemical calculations are performed to study the reactions of OH and ozone with- out and with water to estimate whether the single water molecule can decrease the energy barrier of the OH radical reaction with ozone. The calculated results demonstrate that the single water molecule can reduce the activated barrier of the naked OH+Oa reaction with the value of about 4.18 kJ/mol. In addition, the transition state theory is carried out to determine whether the single water molecule could enhance the rate constant of the OH+O3 reaction. The computed kinetic data indicate that the rate of the ozone reaction with the formed complexes between OH and water is much slower than that of the OH+O3 reaction, whereas the rate constant of OH reaction with the formed H20---Oa complex is 2 times greater than that of the naked OH radical with ozone reaction. However, these processes in the atmosphere are not important because the reactions can not compete well with the naked reaction of OH with ozone under atmospheric condition.
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2011年第4期419-424,I0003,共7页 化学物理学报(英文)
基金 This work was supported by the National Natural Science Foundation of China (No.10865003) and the Science and Technology Foundation of GuiZhou Province, China (No.[201112107). We thank the Key Laboratory of Guizhou High Performance Computational Chemistry for computer time.
关键词 OZONE OH H20 Atmospheric chemistry Quantum chemical calculation 臭氧 羟基 H2O 大气化学 量子化学网格上布鲁塞尔体系化学振荡的粗粒化模拟
分类号 O [理学]
  • 相关文献

参考文献65

  • 1R. P. Wayne, Chemistry of Atmospheres, 3rd Edn., Oxford: Oxford University Press, (2000).
  • 2P. O. Wennberg, R. C. Cohen, R. M. Stimpfle, J. P. Koplow, J. O. Anderson, R. J. Salawitch, D. W. Fahey, E. L. Woodbridge, E. R. Keim, R. S. Gao, C. R. Webster, R. D. May, D. W. Toohey, L. M. Avallone, M. H. Profl:itt, M. Loewenstein, J. R. Podolske, K. R. Chan, and S. C. Wofsy, Science 266, 398 (1994).
  • 3P. O. Wennberg, T. F. Hanisco, L. JaeglT, D. J. Jacob E. J. ttintsa, E. J. Lanzendorf, J. G. Anderson, R. S Gao, E. R. Keim, S. G. Donnelly, L. A. D. Negro, D. W Fahey, S. A. McKeen, R. J. Salawitch, C. R. Webster R. D. May, R. L. Herman, M. H. Proffitt, J. J. Margitan E. L. Atlas, S. M. Schauffter, F. Flocke, C. T. McElroy and T. P. Bui, Science 279, 49 (1998).
  • 4E. J. Lanzendorf, T. F. Hanisco, P. O. Wennberg, R. C. Cohen, R. M. Stimpfle, J. G. Anderson, R. S. Cao, J. J. Margitan, and T. P. Bui, J. Phys. Chem. A 105, 1535 (2001).
  • 5P. S. Monk's, Chem. Soc. Rev. 34, 376 (2005).
  • 6R. L. McKenzie, P. J. Aucamp, A. F. Bais, L. O. Bjorn. M. Ilyas, and S. Madronich, Photochem. Photobiol. Sci. 10, 182 (2011).
  • 7R. Atkinson, D. L. Baulch, R. A. Cox, J. N. Crowley, R F. Hampson, R. G. Hynes, M. E. Jenkin, M. J. Rossi and J. Troe, Atmos. Chem. Phys. 4, 1461 (2004).
  • 8M. J. Kurylo, Chem. Phys. Lett. 23, 467 (1973).
  • 9J. G. Anderson and F. Kaufman, Chem. Phys. Lett. 19 483 (1973).
  • 10A. R. Ravishankara, P. H. Wine, and A. O. Langford, J. Chem. Phys. 70, 984 (1979).

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部