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New Insight for Reaction Route of Hydrogenation of Maleic Anhydride to γ-Butyrolactone

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Abstract

A plausible reaction pathway for maleic anhydride (MA) hydrogenation is firstly proposed, which suggests that the CH4 is produced by the methanation of CO formed during the reaction rather than direct de-carbonization of tetrahydrofuran, and MA cannot be directly decyclized, subsequently de-carbonized to C3 compounds and CO. This work sheds light on the superficial phenomenon for MA liquid hydrogenation reported by other researchers, and may better explain the reaction process both in liquid and vapor phase MA hydrogenation. These results are important to understand the mechanism and reaction pathway of MA hydrogenation, and to facilitate the decrease of production cost in industrial plant.

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References

  1. N. Harris and M.W. Tuck, Hydrocarbon Process 69 (1990) 79.

    Google Scholar 

  2. N.J. Kerrigan, P.C. Hutchison, T.D. Heightman and D.J. Procter, Chem. Commun.1402(2003).

  3. R. Grigg and V. Savic, Chem. Commun.2381(2000).

  4. J.L., D.-J. Choo and Y.H. Kim, Chem. Commun.55(2000).

  5. Y. Hara, H. Kusaka, H. Inagaki, K. Takahashi and K. Wada, J. Catal. 194 (2000) 188.

    Google Scholar 

  6. A. Kuksal, E. Elemm and G. Emig, Appl. Catal. A: Gen. 228 (2002) 237.

    Google Scholar 

  7. U.R. Pillai and E. Sahle-Demessie, Chem. Commun.422 (2002).

  8. U.R. Pillai, E. Sahle-Demessie and D. Young, Appl. Catal. B: Environ. 43 (2003) 131.

    Google Scholar 

  9. A. Cybulski, J. Chrzaszcz and M.V. Twigg, Catal. Today 69 (2001) 241.

    Google Scholar 

  10. S.M. Jung, E. Godard, S.Y. Jung, K.-C. Park and J.U. Choi, Catal. Today 87 (2003) 171.

    Google Scholar 

  11. Y.-L. Zhu, H.-W. **ang, Y.-W. Li, H. Jiao, G.-S. Wu, B. Zhong and G.-Q. Guo, New J. Chem. 27 (2003) 208.

    Google Scholar 

  12. Y.-L. Zhu, H.-W. **ang, G.-S. Wu, L. Bai and Y.-W. Li, Chem. Commun. 254 (2002).

  13. G.L. Castiglioni and C. Fumagalli, US Patent 6297389, 2001).

  14. M. Bergfeld and G. Wiesgickl, US Patent 5536849, 1996).

  15. M.J. Bergfeld and K. Uihlein, US Patent 6075153, (2000).

  16. R.W. Wegman and D.R. Bryant, US Patent 5142067, 1992).

  17. J. Kanetaka, T. Asano and S. Masamune, Ind. Eng. Chem. 62 (1970) 24.

    Google Scholar 

  18. R.M. Deshpande, V.V. Buwa, C.V. Rode, R.V. Chaudhari and P.L. Mills, Catal. Commun. 3 (2002) 269.

    Google Scholar 

  19. M. Messori and A. Vaccari, J. Catal. 150 (1994) 177.

    Google Scholar 

  20. S. Minoda and M. Makoto, Hydrocarbon Process 69 (1990) 176.

    Google Scholar 

  21. U. Herrmann and G. Eming, Ind. Eng. Chem. Res. 37 (1998) 759.

    Google Scholar 

  22. S.P. Müller, M. Kucher, C. Ohlinger and B. Kraushaar-Czarnetzki, J. Catal. 218 (2003) 419.

    Google Scholar 

  23. G.L. Castiglioni, M. Ferrari, A. Guercio, A. Vaccari, R. Lancia and C. Fumagalli, Catal. Today 27 (1996) 181.

    Google Scholar 

  24. V. Pallassana, M. Neurock and G. Coulston, Catal. Today 50 (1999) 589.

    Google Scholar 

  25. K. klusacek and V. Stuchly, Catal. Today 25 (1995) 169.

    Google Scholar 

  26. H. Habazaki, M. Yamasaki, B.P. Zhang, A. Kawashima, S. Kohno, T. Takai and K. Hashimoto, Appl. Catal. A: Gen. 172 (1998) 131.

    Google Scholar 

  27. S.I. Fujiti and N. takezawa, Chem. Eng. J. 68 (1997) 63.

    Google Scholar 

  28. S. Freni, S. Cavallaro, N. Mondello, L. Spadaro and F. Frusteri, J. Power Sources, 108 (2002) 53.

    Google Scholar 

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Correspondence to Yu-Lei Zhu.

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Zhu, YL., Zhao, GW., Chang, J. et al. New Insight for Reaction Route of Hydrogenation of Maleic Anhydride to γ-Butyrolactone. Catalysis Letters 96, 123–127 (2004). https://doi.org/10.1023/B:CATL.0000030109.02546.3f

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  • DOI: https://doi.org/10.1023/B:CATL.0000030109.02546.3f

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