Synthesis and Characterization of Mesoporous Ta−W Oxides as Strong Solid Acid Catalysts
Source abstract
Abstract
Several mesoporous Ta x W 10− x mixed oxides prepared from TaCl 5 and WCl 6 in the presence of poly block copolymer surfactant Pluronic P-123 were examined as potential solid acid catalysts. Amorphous wormhole-type mesopores were observed in samples with x values from 3 to 10, whereas W-rich samples ( x = 0−2) formed nonmesoporous structures with crystallized tungsten oxide (WO 3 ). The acid strength increased with addition of W for mesoporous Ta x W 10− x oxides, and mesoporous Ta 3 W 7 oxide exhibited the highest acid catalytic activity for the Friedel−Crafts alkylation of anisole and the hydrolysis of disaccharides. The results are compared with those of nonporous Ta 2 O 5 −WO 3, HTaWO 6 nanosheets, which were a solid acid obtained by exfoliation and aggregation of layered HTaWO 6 with strong Brønsted acid sites in the interlayer, and a range of conventional solid acid catalysts. Mesoporous Ta−W oxides exhibited a turnover rate higher than that of nonporous Ta 2 O 5 −WO 3 and HTaWO 6 nanosheets, indicating that the mesoporous structure is an advantageous environment for the strong acid sites, because of the high surface area and easy reactant accessibility.
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Research context
OpenAlex topics: Catalysis for Biomass Conversion · Catalysis and Hydrodesulfurization Studies · Polyoxometalates: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical System Engineering, School of Engineering, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan
School of Materials Science, Japan Advanced Institute of Science and Technology (JAIST), 1-1 Asahidai, Nomi, Ishikawa 923-1292, Japan
Chemical Resources Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta Midori-ku, Yokohama 226-8503, Japan
References (38)
Show source-provided references
1. Okuhara T. · Chem. Rev. · 2002 · 102 · 364110.1021/cr0103569 ↗
2. Tanabe K. · Appl. Catal., A · 1999 · 181 · 39910.1016/S0926-860X(98)00397-4 ↗
3. Anastas, P. T.; Williamson, T. C.InGreen Chemistry;Anastas, P. T.; Williamson, T. C.,Eds.American Chemical Society:Washington, DC, 1996; pp1−20.10.1021/bk-1996-0626 ↗
4. Clark J. H. · Green Chem. · 1999 · 1 · 110.1039/a807961g ↗
5. Huang Y.-Y. · Appl. Catal., A · 1996 · 148 · 13510.1016/S0926-860X(96)00223-2 ↗
6. Chidambaram M. · J. Catal. · 2003 · 220 · 44210.1016/S0021-9517(03)00282-3 ↗
7. Landge S. M. · J. Mol. Catal. A: Chem. · 2004 · 213 · 25710.1016/j.molcata.2003.12.022 ↗
8. Hwang C.-C. · J. Phys. Chem. C · 2009 · 113 · 521210.1021/jp810465n ↗
9. Rao Y. · J. Am. Chem. Soc. · 2006 · 128 · 1399610.1021/ja0647147 ↗
10. Rao Y. · J. Am. Chem. Soc. · 2008 · 130 · 39410.1021/ja076584n ↗
11. Kang J. · Angew. Chem., Int. Ed. · 2008 · 47 · 489610.1002/anie.200800721 ↗
12. Tagusagawa C. · Angew. Chem., Int. Ed. · 2010 · 49 · 112810.1002/anie.200904791 ↗
13. Tagusagawa C. · J. Phys. Chem. C · 2009 · 113 · 783110.1021/jp900525a ↗
14. Kondo J. N. · J. Mater. Chem. · 2005 · 15 · 203510.1039/b418331b ↗
15. Parry E. P. · J. Catal. · 1963 · 2 · 37110.1016/0021-9517(63)90102-7 ↗
16. Hughes T. R. · J. Phys. Chem. · 1967 · 71 · 219210.1021/j100866a035 ↗
17. Hino M. · Catal. Commun. · 2004 · 5 · 10710.1016/j.catcom.2003.12.002 ↗
18. Hino M. · Appl. Catal., A · 2006 · 310 · 19010.1016/j.apcata.2006.05.038 ↗
19. Yamashita K. · Catal. Today · 2006 · 118 · 38510.1016/j.cattod.2006.07.025 ↗
20. Shishido T. · Catal. Lett. · 2009 · 129 · 38310.1007/s10562-008-9837-2 ↗
21. Sasaki M. · Ind. Eng. Chem. Res. · 2000 · 39 · 288310.1021/ie990690j ↗
22. Takagaki A. · Chem. Commun. · 2008 · 536310.1039/b810346a ↗
23. Suganuma S. · J. Am. Chem. Soc. · 2008 · 130 · 1278710.1021/ja803983h ↗
24. Onda A. · Green Chem. · 2008 · 10 · 103310.1039/b808471h ↗
25. Rinaldi R. · Angew. Chem., Int. Ed. · 2008 · 47 · 804710.1002/anie.200802879 ↗
26. Chheda J. N. · Angew. Chem., Int. Ed. · 2007 · 46 · 716410.1002/anie.200604274 ↗
27. Corma A. · Chem. Rev. · 2007 · 107 · 241110.1021/cr050989d ↗
28. Iizuka T. · Bull. Chem. Soc. Jpn. · 1983 · 292710.1246/bcsj.56.2927 ↗
29. Tanabe K. · Appl. Catal., A · 1995 · 133 · 19110.1016/0926-860X(95)00205-7 ↗
30. Nowak I. · Chem. Rev. · 1999 · 99 · 360310.1021/cr9800208 ↗
31. Hanaoka T. · Catal. Today · 1990 · 8 · 12310.1016/0920-5861(90)87013-S ↗
32. Hanaoka T. · Catal. Lett. · 1990 · 5 · 1310.1007/BF00772088 ↗
33. Tanabe K. · Mater. Chem. Phys. · 1987 · 17 · 21710.1016/0254-0584(87)90057-5 ↗
34. Tanabe K. · Appl. Catal. A: Gen. · 1995 · 133 · 19110.1016/0926-860X(95)00205-7 ↗
35. Harmer M. A. · Appl. Catal., A · 2001 · 221 · 4510.1016/S0926-860X(01)00794-3 ↗
36. Matsuhashi H. · Phys. Chem. Chem. Phys. · 2004 · 6 · 252910.1039/b316990a ↗
37. Arata K. · Catal. Today · 2003 · 81 · 1710.1016/S0920-5861(03)00098-1 ↗
38. Ross-Medgaarden E. I. · J. Catal. · 2008 · 256 · 10810.1016/j.jcat.2008.03.003 ↗