Superior catalytic performance of Ce1-xBixO2-δ solid solution and Au/Ce1-xBixO2-δ for 5-hydroxymethylfurfural conversion in alkaline aqueous solution

Catalysis Science and Technology

Volumn 5, Issue 2, 2015, Pages 1314-1322

  Miao, Zhenzhen ^a,b   Zhang, Yibo ^a   Pan, Xiqiang ^c   Wu, Tianxiao ^a   Zhang, Bin ^a   Li, Jingwei ^a,b   Yi, Ting ^a,b   Zhang, Zhendong ^a   Yang, Xiangguang ^a  

^a CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c Northwest Research Institute of Chemistry Industry   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; CHEMICAL ACTIVATION; DOPING (ADDITIVES); GOLD; OXYGEN; OXYGEN VACANCIES; PRECIPITATION (CHEMICAL); SOLUTIONS;

2 ,5-FURANDICARBOXYLIC ACIDS; 5 HYDROXYMETHYL FURFURALS; CATALYTIC PERFORMANCE; DEPOSITION PRECIPITATION; HYDRIDE TRANSFERS; HYDROXYMETHYL GROUPS; OXYGEN ACTIVATIONS; SUPPORTING MATERIAL;

SOLID SOLUTIONS;

EID: 84927801909     PISSN: 20444753     EISSN: 20444761     Source Type: Journal    
DOI: 10.1039/c4cy01060d     Document Type: Article

References (48)

1. T. Werpy and G. Petersen, Top Value Added Chemicals from Biomass, Pacific Northwest National Laboratory, 2004, vol. 1, p. 27.
2. Y. Roman-Leshkov, C. J. Barrett, Z. Y. Liu and J. A. Dumesic, Nature, 2007, 447, 982-U985.
3. A. Corma, S. Iborra and A. Velty, Chem. Rev., 2007, 107, 2411-2502.
4. A. Osatiashtiani, A. F. Lee, D. R. Brown, J. A. Melero, G.Morales and K. Wilson, Catal. Sci. Technol., 2014, 4, 333-342.
5. D. A. Kotadia and S. S. Soni, Catal. Sci. Technol., 2013, 3, 469-474.
6. A. S. Amarasekara, D. Green and L. D. Williams, Eur. Polym. J., 2009, 45, 595-598.
7. A. Gandini, ACS Symp. Ser., 1990, 433, 195-208.
8. H. Hirai, J. Macromol. Sci., Chem., 1984, 21, 1165-1179.
9. C. Moreau, M. N. Belgacem and A. Gandini, Top. Catal., 2004, 27, 11-30.
10. P. Vinke, H. E. van Dam and H. van Bekkum, New Dev. Select. Oxidat., 1990, 55, 147-157.
11. P. Verdeguer, N. Merat and A. Gaset, J. Mol. Catal., 1993, 85, 327-344.
12. S. E. Davis, L. R. Houk, E. C. Tamargo, A. K. Datye and R. J. Davis, Catal. Today, 2011, 160, 55-60.
13. S. Subbiah, S. P. Simeonov, J. Esperanca, L. P. N. Rebelo and C. A. M. Afonso, Green Chem., 2013, 15, 2849-2853.
14. B. Saha, S. Dutta and M. M. Abu-Omar, Catal. Sci. Technol., 2012, 2, 79-81.
15. O. Casanova, S. Iborra and A. Corma, ChemSusChem, 2009, 2, 1138-1144.
16. N. K. Gupta, S. Nishimura, A. Takagaki and K. Ebitani, Green Chem., 2011, 13, 824-827.
17. S. E. Davis, B. N. Zope and R. J. Davis, Green Chem., 2012, 14, 143-147.
18. T. Pasini, M. Piccinini, M. Blosi, R. Bonelli, S. Albonetti, N. Dimitratos, J. A. Lopez-Sanchez, M. Sankar, Q. He, C. J. Kiely, G. J. Hutchings and F. Cavani, Green Chem., 2011, 13, 2091-2099.
19. Y. M. Shapiro, V. P. Smolyakov and V. G. Kulnevich, Khim. Geterotsikl. Soedin., 1990, 741-744.
20. G. Hutchings, Gold Bull., 2009, 42, 260-266.
21. Y. Kuwauchi, H. Yoshida, T. Akita, M. Haruta and S. Takeda, Angew. Chem., Int. Ed., 2012, 51, 7729-7733.
22. W. Y. Song and E. J. M. Hensen, Catal. Sci. Technol., 2013, 3, 3020-3029.
23. M. Wang, F. Wang, J. Ma, M. Li, Z. Zhang, Y. Wang, X. Zhang and J. Xu, Chem. Commun., 2014, 50, 292-294.
24. N. Ta, J. Liu, S. Chenna, P. A. Crozier, Y. Li, A. Chen and W. Shen, J. Am. Chem. Soc., 2012, 134, 20585-20588.
25. A. Abad, P. Concepcion, A. Corma and H. Garcia, Angew. Chem., Int. Ed., 2005, 44, 4066-4069.
26. X. Liu, K. Zhou, L. Wang, B. Wang and Y. Li, J. Am. Chem. Soc., 2009, 131, 3140-3141.
27. N. Imanaka, T. Masui, K. Koyabu, K. Minami and T. Egawa, Adv. Mater., 2007, 19, 1608-1611.
28. D. Jiang, W. Wang, E. Gao, L. Zhang and S. Sun, J. Phys. Chem. C, 2013, 117, 24242-24249.
29. L. C. Glaeser, J. F. Brazdil, M. A. Hazle, M. Mehicic and R. K. Grasselli, J. Chem. Soc., Faraday Trans., 1985, 81, 2903-2912.
30. J. Zhu, D. Xiao, J. Li and X. Yang, Catal. Lett., 2009, 129, 240-246.
31. A. Karpenko, R. Leppelt, J. Cai, V. Plzak, A. Chuvilin, U. Kaiser and R. J. Behm, J. Catal., 2007, 250, 139-150.
32. L. Xue, C. Zhang, H. He and Y. Teraoka, Catal. Today, 2007, 126, 449-455.
33. Z. Ma, H. Yin, S. Overbury and S. Dai, Catal. Lett., 2008, 126, 20-30.
34. L. Li, F. Chen, J.-Q. Lu and M.-F. Luo, J. Phys. Chem. A, 2011, 115, 7972-7977.
35. I. Kosacki, T. Suzuki, H. U. Anderson and P. Colomban, Solid State Ionics, 2002, 149, 99-105.
36. M. Guo, J. Lu, Y. Wu, Y. Wang and M. Luo, Langmuir, 2011, 27, 3872-3877.
37. L. Kumari, J. H. Lin and Y. R. Ma, J. Phys.: Condens. Matter, 2007, 19, 406204.
38. V. N. Denisov, A. N. Ivlev, A. S. Lipin, B. N. Mavrin and V. G. Orlov, J. Phys.: Condens. Matter, 1997, 9, 4967-4978.
39. S. Goswami, S. Dey and S. Jana, Tetrahedron, 2008, 64, 6358-6363.
40. O. Casanova, S. Iborra and A. Corma, J. Catal., 2009, 265, 109-116.
41. J. Guzman, S. Carrettin, J. C. Fierro-Gonzalez, Y. L. Hao, B. C. Gates and A. Corma, Angew. Chem., Int. Ed., 2005, 44, 4778-4781.
42. J. Beckers, A. F. Lee and G. Rothenberg, Adv. Synth. Catal., 2009, 351, 1557-1566.
43. R. Sumathi, K. Johnson, B. Viswanathan and T. K. Varadarajan, Appl. Catal., A, 1998, 172, 15-22.
44. M. Sankar, E. Nowicka, R. Tiruvalam, Q. He, S. H. Taylor, C. J. Kiely, D. Bethell, D. W. Knight and G. J. Hutchings, Chem. - Eur. J., 2011, 17, 6524-6532.
45. A. Abad, C. Almela, A. Corma and H. Garcia, Tetrahedron, 2006, 62, 6666-6672.
46. B. T. Teng, J. J. Lang, X. D. Wen, C. Zhang, M. H. Fan and H. G. Harris, J. Phys. Chem. C, 2013, 117, 18986-18993.
47. R. Si and M. Flytzani-Stephanopoulos, Angew. Chem., 2008, 120, 2926-2929.
48. J. Yang, Y. J. Guan, T. Verhoeven, R. van Santen, C. Li and E. J. M. Hensen, Green Chem., 2009, 11, 322-325.