详细信息
A study of n-hexane hydroisomerization catalyzed with the Pt/H3PW12O40/Zr-MCM-41 catalysts ( EI收录)
文献类型:期刊文献
英文题名:A study of n-hexane hydroisomerization catalyzed with the Pt/H3PW12O40/Zr-MCM-41 catalysts
作者:Chen, L.F.[1]; Nore?a, L.E.[2]; Wang, J.A.[1]; Zhou, X.L.[3]; Navarrete, J.[4]; Hernández, I.[2]; Montoya, A.[4]; Romo, P. Pérez[4]; Salas, P.[5]; Pergher, S. Castella[6]
机构:[1] ESIQIE, Instituto Politécnico Nacional, Col. Zacatenco, 07738 México, D.F., Mexico; [2] Departamento de Ciencias Básicas, Universidad Autónoma Metropolitana-A, Av. San Pablo 180, Col. Reynosa-Tamaulipas, 02200 México, D.F., Mexico; [3] Petroleum Processing Research Center, East China University of Science and Technology, Shanghai, 200237, China; [4] Grupo de Molecular Ingeniería, Instituto Mexicano del Petróleo, Eje Lazaro Cardenas 152, 07730 México, D.F., Mexico; [5] Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, A.P. 1-1010, 76000 Querétaro, Mexico; [6] Universidad Regional Intergrada do Alto Uruguai e das Missoes, Campus Erechim, URI, C.P. 743, Brazil
年份:2008
卷号:133-135
期号:1-4
起止页码:331
外文期刊名:Catalysis Today
收录:EI(收录号:20081411182455)
语种:英文
外文关键词:Catalysis - Catalyst activity - Isomerization - Platinum compounds - X ray diffraction
摘要:A series of Zr-modified MCM-41 mesoporous materials with a variety of Si/Zr molar ratios were synthesized by the surfactant-templated method. Textural properties, crystalline structure and surface acidity were characterized by X-ray diffraction (XRD), low-temperature N2 physisorption isotherms, solid-state nuclear magnetic resonance (MAS-NMR), UV-visible spectroscopy, and Fourier-transform infrared (FTIR) spectroscopy of pyridine adsorption techniques. Both the as-made and the calcined materials show the typical MCM-41 structure with hexagonal mesochannels. The structural regularity varies with zirconium content in the materials. A proper amount of zirconium ions incorporated into the Si framework may noticeably improve the structural order, but high zirconium content leads to the reduction of the structural regularity. The mean pore diameter of the materials increases from 2.8 to 3.0, 3.8 and 4.5 nm as the Si/Zr molar ratio decreases from 25 to 15, 8 and 4, respectively. Meanwhile, the surface area and pore volume diminish with the increase of zirconium content. As H3PW12O40 (referred as HPW) is dispersed on the Zr-MCM-41 materials, the Br?nsted acidity is greatly enhanced: from four to eight times. Three forms of heteropolyanions: (i) bulk-like HPW particles, (ii) highly dispersed HPW clusters with deformed Keggin structure and (iii) HPW species with partially fragmented Keggin structure, are adopted by the HPW deposited on the Zr-MCM-41 solids, due to the different interactions between the heteropolyacid species and the support. The 1 wt.%Pt/25 wt.%HPW/Zr-MCM-41 catalysts show high activity for the n-hexane hydroisomerization reaction, with 100% selectivity to isohexanes at temperatures below 260 °C. Increasing the zirconium content generally leads to a higher n-hexane conversion but it lowers the selectivity to hexane isomers that might be related to the different pore diameter distribution and surface density of the Br?nsted acid sites. ? 2008 Elsevier B.V. All rights reserved.
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