journal article·2013-03

Nanorods-assembled CeVO4 hollow spheres as active catalyst for oxidative dehydrogenation of propane

Feng Luo, Chun-Jiang Jia, Rui Liu, Ling-Dong Sun, Chun-Hua Yan

Materials Research Bulletin· Volume 48· Issue 3
Publisher page

Abstract

Abstract CeVO 4 hollow sphere nanostructures have been prepared by a simple hydrothermal synthesis method. HRTEM investigation indicates that the CeVO 4 hollow spheres are assembled by small single crystal nanorods. Through a plus post annealing treatment at 500 °C, the CeVO 4 hollow spheres have more Ce 4+ species (Ce 4+ /(Ce 4+ + Ce 3+ ) is ca. 5%) in the surface compared with the as-prepared sample (ca. 1%) based on the XPS results. No CeO 2 and V 2 O 5 phases were examined by both XRD and Raman spectroscopy, which indicates that Ce 3+ –Ce 4+ /V 5+ –V 4+ coexist in the annealed CeVO 4 hollow spheres, confirmed by the existence of V 4+ detected by XPS. At 500 °C, the nanorods assembled CeVO 4 hollow spheres exhibits a rather very high selectivity (ca. 70%) for propylene in oxidative dehydrogenation (ODH) reaction of propane. The presence of Ce 4+ , which induces additional V 4+ in these hollow sphere nanostructures, is critical for the enhancement of selectivity of the catalyst.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Catalysis and Oxidation Reactions · Catalytic Processes in Materials Science · Luminescence Properties of Advanced Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (35)

Show source-provided references
1. Cavani · Catal. Today · 2007 · 127 · 11310.1016/j.cattod.2007.05.009 ↗
2. Koc · J. Mol. Catal. A: Chem. · 2005 · 225 · 19710.1016/j.molcata.2004.09.009 ↗
3. Watson · J. Catal. · 2000 · 191 · 1210.1006/jcat.1999.2781 ↗
4. Lezla · J. Catal. · 1997 · 170 · 34610.1006/jcat.1997.1759 ↗
5. Routray · Appl. Catal. A: Gen. · 2004 · 265 · 10310.1016/j.apcata.2004.01.006 ↗
6. Dinsea · J. Mol. Catal. A: Chem. · 2008 · 289 · 2810.1016/j.molcata.2008.04.007 ↗
7. Sam · J. Catal. · 1990 · 123 · 41710.1016/0021-9517(90)90139-B ↗
8. Guerrero-Ruiz · Stud. Surf. Sci. Catal. · 1992 · 72 · 20310.1016/S0167-2991(08)61672-9 ↗
9. Wachs · Catal. Today · 2005 · 100 · 7910.1016/j.cattod.2004.12.019 ↗
10. Daniell · Top. Catal. · 2002 · 20 · 6510.1023/A:1016399315511 ↗
11. Reddy · J. Phys. Chem. C · 2007 · 111 · 1875110.1021/jp076617l ↗
12. Beckers · Green Chem. · 2010 · 12 · 93910.1039/c000191k ↗
13. Burcham · Top. Catal. · 2000 · 85 · 11
14. Martínez-Huerta · J. Phys. Chem. C · 2008 · 112 · 1144110.1021/jp802827t ↗
15. Taylor · Top. Catal. · 2009 · 52 · 166010.1007/s11244-009-9307-0 ↗
16. Wong · Surf. Sci. · 2002 · 498 · 26610.1016/S0039-6028(01)01761-7 ↗
17. Ganduglia-Pirovano · J. Am. Chem. Soc. · 2010 · 132 · 234510.1021/ja910574h ↗
18. Martínez-Huerta · J. Catal. · 2004 · 225 · 24010.1016/j.jcat.2004.04.005 ↗
19. Luo · Cryst. Growth Des. · 2005 · 5 · 13710.1021/cg049940b ↗
20. 1998
21. Reddy · J. Phys. Chem. B · 2002 · 106 · 1096410.1021/jp021195v ↗
22. Pfau · Surf. Sci. · 1994 · 321 · 7110.1016/0039-6028(94)90027-2 ↗
23. Nguyen · Langmuir · 2009 · 25 · 1114210.1021/la901387q ↗
24. Irvine · Adv. Mater. · 1990 · 2 · 13210.1002/adma.19900020304 ↗
25. 1987
26. Tsipis · J. Mater. Chem. · 2002 · 12 · 373810.1039/B206004C ↗
27. Tuller · Sold State Ionics · 2000 · 131 · 14310.1016/S0167-2738(00)00629-9 ↗
28. Gaur · J. Mater. Sci. · 1985 · 20 · 316710.1007/BF00545182 ↗
29. Au · J. Chem. Soc. Faraday Trans. · 1997 · 93 · 119510.1039/a607565g ↗
30. Au · Catal. Lett. · 1996 · 37 · 24110.1007/BF00807761 ↗
31. Fang · Catal. Lett. · 1999 · 61 · 3910.1023/A:1019096116289 ↗
32. Zhang · Appl. Catal. A: · 1999 · 181 · 6310.1016/S0926-860X(98)00412-8 ↗
33. Sokolovskii · J. Catal. · 1997 · 167 · 29610.1006/jcat.1997.1564 ↗
34. Wagner · 1978
35. Echigoya · 1984 · 5