A selective synthesis of 1-phenylethanol and γ-butyrolactone through coupling processes over Cu/MgO catalysts

Journal of Molecular Catalysis A: Chemical

Volumn 355, Issue , 2012, Pages 180-185

  Reddy, Kannapu Hari Prasad ^a   Anand, Narani ^a   Venkateswarlu, Vakati ^a   Rao, Kamaraju Seetha Rama ^a   Burri, David Raju ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Butyrolactone; 1,4 Butanediol; 1 Phenylethanol; Acetophenone; Hydrogen

Indexed keywords

1 ,4-BUTANEDIOL; 1-PHENYLETHANOL; ACETOPHENONES; BET SURFACE AREA; BUTYROLACTONES; COUPLING PROCESS; CU/MGO CATALYSTS; HIGHER YIELD; IMPREGNATION METHODS; SELECTIVE SYNTHESIS; TEMPERATURE-PROGRAMMED REDUCTION; VAPOR PHASE; XRD;

ATMOSPHERIC PRESSURE; CATALYST ACTIVITY; CHEMISORPTION; ETHANOL; HYDROGEN; KETONES; TRANSMISSION ELECTRON MICROSCOPY; X RAY PHOTOELECTRON SPECTROSCOPY;

CATALYST SELECTIVITY;

EID: 84856112510     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2011.12.014     Document Type: Article

References (31)

1. Y. Kashiwagi, K. Uchiyama, F. Kurashima, C. Kikuchi, and J. Anzai Chem. Pharm. Bull. 47 1999 1051 1052
2. K. Hari Prasad Reddy, R. Rahul, S. Sree Vardhan Reddy, B. David Raju, and K.S. Rama Rao Catal. Commun. 10 2009 879 883
3. R.V. Malyala, C.V. Rode, M. Arai, S.G. Hegde, and R.V. Chaudhari Appl. Catal. A: Gen. 193 2000 71 86
4. M. Casagrande, L. Storaro, A. Talon, M. Lenarda, R. Frattini, E.R. Castellón, and P.M. Torres J. Mol. Catal. A: Chem. 188 2002 133 139
5. Y. Sun, Y. Guo, Q. Lu, X. Meng, W. Xiaohau, Y. Guo, Y. Wang, X. Liu, and Z. Zhang Catal. Lett. 100 2005 213 217
6. M. Lenarda, M. Casagrande, E. Moretti, L. Storaro, R. Frattini, and S. Polizzib Catal. Lett. 114 2007 79 84
7. J. Masson, P. Cividino, and J. Court Appl. Catal. A: Gen. 161 1997 191 197
8. N.M. Bertero, C.R. Apesteguia, and A.J. Marchi Appl. Catal. A: Gen. 349 2008 100 109
9. C.-S. Chen, and H.-W. Chen Appl. Catal. A: Gen. 260 2004 207 213
10. C.-S. Chen, H.-W. Chen, and W.-H. Cheng Appl. Catal. A: Gen. 248 2003 117 218
11. Y.-L. Zu, J. Yang, G.-Q. Dong, H.-Y. Zheng, H.-H. Zhang, H.-W. Xiang, and Y.-W. Li Appl. Catal. B: Environ. 57 2005 183 190
12. K. Hari Prasad Reddy, N. Anand, P.S. Sai Prasad, K.S. Rama Rao, and B. David Raju Catal. Commun. 12 2011 866 869
13. H.E. Bellis, US Patent No. 5,110,954, 1992.
14. R. Sigg, H. Regner, US Patent No. 5,426,195, 1995.
15. H.J. Mercker, F.F. Pape, J. Simon, A. Henne, M. Hesse, U. Kohler, R. Dostalek, C. Freire, H. Krutz, US Patent No. 5,955,620, 1999.
16. D. Zhang, H. Yin, R. Zhang, J. Xue, and T. Jiang Catal. Lett. 122 2008 176 182
17. H.Y. Zheng, Y.L. Zhu, Z.Q. Bai, L. Huang, H.W. Xiang, and Y.W. Li Green Chem. 8 2006 107 109
18. Y.L. Zhu, H.W. Xiang, Y.W. Li, H. Jiao, G.S. Wu, B. Zhong, and G.Q. Guo New J. Chem. 27 2003 208 210
19. A. Sun, Z. Qin, and J. Wang Catal. Lett. 79 2002 33 37
20. Y.L. Zhu, H.W. Xiang, G.S. Wu, L. Bai, and Y.W. Li Chem. Commun. 3 2002 254 255
21. K.S. Rama Rao, B. David Raju, S. Narayanan, B.M. Nagaraja, A.H. Padmasri, V. Siva Kumar, US patent No. 7015359B1, 2008.
22. B.M. Nagaraja, A.H. Padmasri, P. Seetharamulu, K. Hari Prasad Reddy, B. David Raju, and K.S. Rama Rao J. Mol. Catal. A: Chem. 278 2007 29 37
23. G. Brieger, and T.J. Nestrick Chem. Rev. 74 5 1974 567 580
24. C.T. Campbell Surf. Sci. Rep. 27 1997 1 111
25. J.W. He, and P.J. Moller Surf. Sci. 180 1987 411 420
26. B.M. Nagaraja, V. Siva Kumar, V. Sashikala, A.H. Padmasri, B. Sreedhar, B. David Raju, and K.S. Rama Rao Catal. Commun. 4 2003 287 293
27. T. Nanba, S. Masukawa, J. Uchisawa, and A. Obuchi Catal. Lett. 93 2004 195 201
28. F.E. Lopez-Suarez, A. Bueno-Lopez, and M.J. lllan-Gomez Appl. Catal. B: Environ. 84 2008 651 658
29. K.S. Kim J. Electron Spectrosc. Relat. Phenom. 3 1974 217 226
30. G. Avgouropoulos, and T. Ioannides Appl. Catal. A: Gen. 244 2003 155 167
31. E.C. Kleiderer, and E.C. Kornfeld J. Org. Chem. 13 1948 455 458