Selective Oxidation of Ethane over SBA-15 Mesoporous Zeolite Supported Vanadium-Based Oxide Catalysts

被引:5
|
作者
Liu Jian [1 ]
Zhao Zhen [1 ]
Zhang Zhe [1 ]
Xu Chun-Ming [1 ]
Duan Ai-Jun [1 ]
Jiang Gui-Yuan [1 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Catalyst; Ethane; Selective oxidation; SBA-15; Supported-vanadium oxide; K-modification; SILICA; DEHYDROGENATION; FORMALDEHYDE; REACTIVITY; METHANE;
D O I
10.3866/PKU.WHXB20091118
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
A series of SBA-15 supported vanadium oxide (V/SBA-15) and K-modified vanadium oxide (K-V/SBA15) catalysts with different active components were prepared by incipient-wetness impregnation. The structures of the catalysts were characterized using N-2 adsorption, low angle X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and UV-Raman spectroscopy techniques. Their catalytic performances for the selective oxidation of ethane were also investigated. The results showed that SBA-15 was a better support for the catalyst system than SiO2 for the selective oxidation of ethane to aldehydes. The SBA-15-supported low loading catalyst was a highly dispersed catalyst system and the SBA-15 supported K-V samples with low loading (n(v):n(Si) <= 5.0:100) had ordered hexagonal mesostructures. For the V/SBA-15 and K-V/SBA-15 catalysts, isolated vanadyl species with tetrahedral coordination are determined to be the active sites for aldehyde formation at very low vanadium loading (n(v):n(Si) <= 0.1:100). The polymeric vanadyl species with octahedral coordination and the microcrystalline vanadium oxide constitute the active sites for the oxidative dehydrogenation or deep oxidation of ethane when the loading of vanadium is higher than 2.5:100.
引用
收藏
页码:2467 / 2474
页数:8
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