Molecular approaches towards mixed metal oxides and their behaviour in mixed oxide support Au catalysts for CO oxidation

被引:25
作者
Geserick, Jasmin [1 ]
Froeschl, Thomas [1 ]
Huesing, Nicola [1 ]
Kucerova, Gabriela [2 ]
Makosch, Martin [2 ]
Diemant, Thomas [2 ]
Eckle, Stephan [2 ]
Behm, R. Juergen [2 ]
机构
[1] Univ Ulm, Inst Inorgan Chem 1, D-89069 Ulm, Germany
[2] Univ Ulm, Inst Catalysis & Surface Chem, D-89069 Ulm, Germany
关键词
TEMPERATURE-PROGRAMMED DESORPTION; MESOPOROUS AU/TIO2 CATALYSTS; GOLD CATALYSTS; TITANIA-SILICA; CARBON-MONOXIDE; ACTIVE GOLD; MODIFIED SILANES; PARTICLE-SIZE; SURFACE-AREA; THIN-FILMS;
D O I
10.1039/c0dt00911c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We herein report a water-based sol-gel approach towards porous mixed Si/Ti oxides using co-precipitated glycol-modified precursors. By adjusting synthesis parameters such as the pH value and the Si/Ti ratio of the precursor, the morphology as well as the Si/Ti-composition of the resulting mixed oxide particles can be varied in a wide range. The behaviour of the mixed oxides as substrates for Au catalysts and the performance of the resulting catalysts in the CO oxidation reaction was investigated and compared to catalysts supported on mesoporous anatase and rutile synthesized analogously. For comparable Au particle sizes and Au loadings, the composition of the mixed oxide support was found to significantly affect the reactivity and reaction behaviour, with mixed oxide supported Au catalysts synthesized at pH = 5 or 10 and with a Si/Ti-ratio of 1 : 19 and 1 : 34 exhibiting the maximum activity. In contrast to the enhanced activity, the mixed oxide supports do not lead to a significant improvement in deactivation behaviour and catalyst stability.
引用
收藏
页码:3269 / 3286
页数:18
相关论文
共 101 条
[1]  
[Anonymous], 1995, Handbook of X-ray Photoelectron Spectroscopy. A Reference Book of Standard Spectra for Identification and Interpretation of XPS Data
[2]   Nanosize rutile titania particle synthesis via a hydrothermal method without mineralizers [J].
Aruna, ST ;
Tirosh, S ;
Zaban, A .
JOURNAL OF MATERIALS CHEMISTRY, 2000, 10 (10) :2388-2391
[3]   The influence of the preparation methods on the catalytic activity of platinum and gold supported on TiO2 for CO oxidation [J].
Bamwenda, GR ;
Tsubota, S ;
Nakamura, T ;
Haruta, M .
CATALYSIS LETTERS, 1997, 44 (1-2) :83-87
[4]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[5]   Au/TiO2 nanosized samples:: A catalytic, TEM, and FTIR study of the effect of calcination temperature on the CO oxidation [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M ;
Lu, P ;
Akita, T ;
Ichikawa, S ;
Haruta, M .
JOURNAL OF CATALYSIS, 2001, 202 (02) :256-267
[6]   Au/TiO2 nanostructured catalyst:: effects of gold particle sizes on CO oxidation at 90 K [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M .
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 2001, 15 (1-2) :215-217
[7]   Cultivation of human fibroblasts and multipotent mesenchymal stromal cells on mesoporous silica and mixed metal oxide films [J].
Boecking, D. ;
Fiedler, J. ;
Brenner, R. E. ;
Huesing, N. .
JOURNAL OF MATERIALS SCIENCE, 2009, 44 (24) :6786-6794
[8]  
Bond G. C., 2007, CATALYSIS GOLD, P161
[9]   Simultaneous drying and chemical modification of hierarchically organized silica monoliths with organofunctional silanes [J].
Brandhuber, D ;
Peterlik, H ;
Hüsing, N .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (35-36) :3896-3902
[10]  
Brinker C. J., 1990, SOL GEL SCI