Investigation of the structure and activity of VOx/CeO2/SiO2 catalysts for methanol oxidation to formaldehyde

被引:36
作者
Vining, William C.
Strunk, Jennifer
Bell, Alexis T. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
Methanol oxidation; Vanadia; Ceria; Silica; SUPPORTED VANADIUM-OXIDE; HIGH-SURFACE-AREA; SELECTIVE OXIDATION; RUTILE TIO2(110); DYNAMIC STATES; SILICA; RAMAN; XPS; SPECTROSCOPY; CEO2(111);
D O I
10.1016/j.jcat.2011.09.024
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
The effect of ceria on the partial oxidation of methanol to formaldehyde over VOx/CeO2/SiO2 catalysts was investigated. A two-dimensional layer of ceria on silica was prepared by grafting cerium (IV) t-butoxide (Ce(OC4H9)(4)) onto high surface area, mesoporous silica, SBA-15, and then calcining the resulting product in air at 773 K. Ce surface concentrations obtained this way ranged from 0.2 to 0.9 Ce nm(-2). Next, V was introduced by grafting VO((OPr)-Pr-i)(3) onto CeO2/SiO2 in order to achieve a surface concentration of 0.6 V nm(-2). XANEs spectra indicate that all of the V is in the 5+ oxidation state and Raman spectra show that vanadia exist as pseudo-tetrahedra bonded to either silica or ceria. Data from Raman spectroscopy and temperature-programmed desorption of adsorbed methanol indicate that with increasing Ce surface density, most of the V becomes associated with the deposited ceria. The turnover frequency for methanol oxidation is nearly two orders of magnitude higher for VOx/CeO2/SiO2 than for VOx/SiO2, whereas the apparent activation energy and apparent first-order pre-exponential factor are 17 kcal/mol and 1.4 x 10(6) mol CH2O (mol V atm s)(-1), respectively, for VOx(/)CeO(2)/SiO2 and 23 kcal/mol and 2.3 x 10(7) mol CH2O (mol V atm s)(-1), respectively, for VOx/SiO2. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:160 / 167
页数:8
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