Effect of the surfactant on the nanostructure of mesoporous Pt/Mn/WOx/ZrO2 catalysts and their catalytic activity in the hydroisomerization of n-hexane

被引:27
作者
Hernández, ML
Montoya, JA
Hernández, I
Viniegra, M
Llanos, ME
Garibay, V
Del Angel, P
机构
[1] Inst Mexicano Petr, Programa Ingn Mol, Mexico City 07730, DF, Mexico
[2] Univ Autonoma Metropolitana Azcapotzalco, Mexico City 02200, DF, Mexico
[3] Univ Autonoma Metropolitana Iztapalapa, Mexico City 09340, DF, Mexico
关键词
tungstated zirconia; manganese; surfactant; mesoporous solids; n-hexane hydroisomerization; HRTEM;
D O I
10.1016/j.micromeso.2005.10.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The influence of the cetyl-trimethylammonium bromide (CTAB) as a surfactant over the nanostructure and reactivity of mesoporous Pt/Mn/WOx/ZrO2 materials synthesized by the coprecipitation method and calcined at 800 degrees C was studied. The Mn/WOx/ZrO2 materials were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), nitrogen adsorption-desorption, and Raman spectroscopy. Their catalytic performance was evaluated on the n-hexane hydroisomerization reaction using the platinum impregnated samples. The results show that the metastable tetragonal zirconia phase was favored by the addition of 1.0 wt.% manganese. The surfactant incorporation in different molar ratios (CTAB/ZrO2) leads to mesoporous solids with higher surface area and narrow pore size distribution. The surface area, pore size and pore size distribution depend on the CTAB/ZrO2 molar ratio. Laser Raman spectroscopy and Rietveld refinement of the crystalline phases confirmed that only a fraction of tungsten (approximate to 5 wt.%) leads to the formation of the WO3 crystalline phase and the reminder is highly dispersed forming amorphous polytungstate species on the zirconia surface. These WOx species are accessible to the n-hexane molecule, leading to an increase in the catalytic activity and selectivity to the biramified products (2,2-DMB and 2,3-DMB). (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:186 / 195
页数:10
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