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Computational Studies on the Sulfur Dioxide Absorption by Organic Lewis Bases

  • Shim, Jae-Goo (Global Environment Research Group, Environment & Structure Laboratory, Korea Electric Power Research Institute) ;
  • Jhon, Young-H. (Department of Chemistry and CAMDRC, Soongsil University) ;
  • Kim, Jun-Han (Global Environment Research Group, Environment & Structure Laboratory, Korea Electric Power Research Institute) ;
  • Jang, Kyung-Ryong (Global Environment Research Group, Environment & Structure Laboratory, Korea Electric Power Research Institute) ;
  • Kim, Ja-Heon (Department of Chemistry and CAMDRC, Soongsil University)
  • Published : 2007.09.20

Abstract

Keywords

References

  1. Gleason, G. H.; Montclair, N. J.; Loonam A. C. U.S. Patent 21106453, 1940
  2. Heisel, M.; Bellani, A. Gas Sep. Pur. 1991, 5, 111 https://doi.org/10.1016/0950-4214(91)80007-R
  3. Hass, R. H.; Albertson, W. U.S. Patent 4347227, 1982
  4. Jones, M. B.; Fowler, A. E. U.S. Patent 4530704, 1985
  5. Terybig, D. S.; Potter, J. L.; Jones, M. B.; Motes, J. M. U.S. Patent 4783327, 1988
  6. Christiansen, S. H.; Chang, D.; Crump, D. K. U.S. Patent 5098681, 1992
  7. Chang, D.; Bedell, S. A.; Kirby, L. H. U.S. Patent 5433934, 1995
  8. van Dam, M. H. H.; Lamine, A. S.; Roizard, D.; Lochon, P.; Roizard, C. Ind. Eng. Chem. Res. 1997, 36, 4628-4637 https://doi.org/10.1021/ie970111f
  9. Kermadec, R. D.; Lapicque, F.; Roizard, D.; Roizard, C. Ind. Eng. Chem. Res. 2002, 41, 153-163 https://doi.org/10.1021/ie010173c
  10. Sartori, G.; Savage, D. W. Ind. Eng. Chem. Fundam. 1987, 22, 239-249 https://doi.org/10.1021/i100010a016
  11. Oh, J. J.; LaBarge, M. S.; Matos, J.; Kampf, J. W.; Hillig II, K. W.; Kuczkkowski, R. L. J. Am. Chem. Soc. 1991, 113, 4732-4738 https://doi.org/10.1021/ja00013a003
  12. Oh, J. J.; Hillig II, K. W.; Kuczkowski, R. L. J. Phys. Chem. 1991, 95, 7211-7216 https://doi.org/10.1021/j100172a022
  13. Oh, J. J.; Hillig II, K. W.; Kuczkowski, R. L. Inorg. Chem. 1991, 30, 4583-3588 https://doi.org/10.1021/ic00024a025
  14. Oh, J. J.; Hillig II, K. W.; Kuczkowski, R. L. J. Am. Chem. Soc. 1991, 113, 7480-7484 https://doi.org/10.1021/ja00020a004
  15. Leopold, K. R.; Canagaratna, M.; Phillips, J. A. Acc. Chem. Res. 1997, 30, 57-64 https://doi.org/10.1021/ar950115l
  16. Bondi, A. J. Phys. Chem. 1964, 68, 441-451 https://doi.org/10.1021/j100785a001
  17. Grundnes, J.; Christian, S. D. J. Am. Chem. Soc. 1968, 90, 2239-2245 https://doi.org/10.1021/ja01011a006
  18. Gutmann, V. The Donor-Acceptor Approach to Molecular Interactions; Plenum press: New York. U. S. A., 1978
  19. Gojlo, E.; Gampe, T.; Krakowiak, J.; Stangret, J. J. Phys. Chem. A 2007, 111, 1827-1834 https://doi.org/10.1021/jp065599p
  20. Pearson, R. G. J. Am. Chem. Soc. 1986, 108, 6109-6114 https://doi.org/10.1021/ja00280a002
  21. Arnentt, E. M.; Mitchell, E. J.; Murty, T. S. S. R. J. Am. Chem. Soc. 1974, 96, 3875-3876 https://doi.org/10.1021/ja00819a028
  22. Perin, D. D. Dissociation Constants of Organic Bases in Aqueous Solution; Butterworths: London, U. K., 1965; Supplement, 1972
  23. Young, D. C. Computational Chemistry; A John-Wiley & Sons, Inc.: 2001
  24. Miertus, S.; Scrocco, E.; Tomasi, J. Chem. Phys. 1981, 55, 117 https://doi.org/10.1016/0301-0104(81)85090-2
  25. Boys, S. F.; Bernardi, F. Mol. Phys. 1970, 19, 553 https://doi.org/10.1080/00268977000101561

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