Spectroscopic characterization of highly dispersed vanadia supported on SBA-15

被引:95
作者
Hess, C
Hoefelmeyer, JD
Tilley, TD
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
D O I
10.1021/jp037714r
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Spectroscopic analysis was used to gain new insight into the molecular structures occurring during the synthesis of highly dispersed silica SBA-15 supported vanadia (VOx/SBA-15). VOx/SBA-15 was prepared by a grafting/anion-exchange procedure. As a first step of the procedure, the inner pores of SBA-15 are functionalized via grafting of 3-aminopropyltrimethoxysilane. After fort-nation of the corresponding ammonium salt, decavanadate (V10O286-) is incorporated into the pores by anion exchange. In the final step, calcination of the decavanadate precursor, yields the chemically bonded vanadia species. Using this approach, vanadium loadings of up to 22 wt % of V on SBA-15 were obtained. As followed by Raman spectroscopy, upon dehydration, the structure of the supported vanadia changes dramatically. Raman and diffuse reflectance UV-vis spectroscopy under dehydrated conditions reveal the presence of different vanadia structures (monomers, polymers, and crystals) as a function of vanadium loading (0-22 wt % of V). The maximum coverage of vanadia species on SBA-15 is achieved at 7.2 wt % of V (2.3 V/nm(2)). At loadings up to 7.2 wt % of V, the vanadia species are mainly present as isolated tetrahedral species, whereas at higher loadings V2O5 crystallites are formed, in addition to monomeric and polymeric vanadia species.
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页码:9703 / 9709
页数:7
相关论文
共 58 条
[21]   ELEMENTARY SURFACE-REACTIONS IN THE PREPARATION OF VANADIUM-OXIDE OVERLAYERS ON SILICA BY CHEMICAL VAPOR-DEPOSITION [J].
INUMARU, K ;
OKUHARA, T ;
MISONO, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (12) :4826-4832
[22]   Structure and catalysis of vanadium oxide overlayers on oxide supports [J].
Inumaru, K ;
Misono, M ;
Okuhara, T .
APPLIED CATALYSIS A-GENERAL, 1997, 149 (01) :133-149
[23]   THE ROLE OF V=O SITES ON THE OXIDATION OF METHANE TO FORMALDEHYDE OVER V/SIO2 [J].
IRUSTA, S ;
CORNAGLIA, LM ;
MIRO, EE ;
LOMBARDO, EA .
JOURNAL OF CATALYSIS, 1995, 156 (01) :167-170
[24]  
ISHII Y, 1991, J AM CERAM SOC, V74, P2324, DOI 10.1111/j.1151-2916.1991.tb08308.x
[25]   Silica-supported, single-site titanium catalysts for olefin epoxidation. A molecular precursor strategy for control of catalyst structure [J].
Jarupatrakorn, J ;
Tilley, JD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (28) :8380-8388
[26]  
Jeng J.M., 1996, CATAL TODAY, V28, P335
[27]  
JOHNSON B, 1988, J CHEM SOC P1, V84, P1897
[28]   Surface-controlled gas-phase deposition and characterization of highly dispersed vanadia on silica [J].
Keranen, J ;
Guimon, C ;
Iiskola, E ;
Auroux, A ;
Niinisto, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (39) :10773-10784
[29]   SURFACE-STRUCTURE AND REACTIVITY OF CRO3/SIO2 CATALYSTS [J].
KIM, DS ;
TATIBOUET, JM ;
WACHS, IE .
JOURNAL OF CATALYSIS, 1992, 136 (01) :209-221
[30]   REFINEMENT OF STRUCTURE OF MG3(VO4)2 [J].
KRISHNAMACHARI, N ;
CALVO, C .
CANADIAN JOURNAL OF CHEMISTRY-BACK YEAR, 1971, 49 (10) :1629-+