Catalytic oxidation of ethane with oxygen using fluidised nanoparticle NiO catalyst

被引:21
作者
Syed-Hassan, Syed Shatir A. [1 ,2 ]
Li, Chun-Zhu [1 ,2 ]
机构
[1] Curtin Univ Technol, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
[2] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
Fluidised nanoparticle catalyst; Radical desorption; Light hydrocarbon conversion; Catalytic oxidation; Ethane; Nickel oxide; NICKEL MESH CATALYST; O MIXED OXIDES; GAS-PHASE; SELECTIVE CATALYSTS; ETHENE PRODUCTION; LOW-TEMPERATURE; COKE FORMATION; DEHYDROGENATION; PYROLYSIS; RADICALS;
D O I
10.1016/j.apcata.2011.08.008
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
In a typical industrial catalyst, a small amount of catalytically active species is finely dispersed inside a large amount of porous support material. The reactor volume is mainly occupied by the catalyst support, not by the catalytic species itself. The use of fluidised nanoparticles as catalyst without the need of a support may result in drastic reduction in catalytic reactor volume for major savings in capital and operating costs. Here we report for the first time the use of fluidised NiO nanoparticles to catalyse ethane-oxygen reaction at temperatures of 240-420 degrees C. Our data indicate that the fluidised NiO nanoparticles exhibit very different characteristics from the traditional porous catalyst. The lack of a rigid porous structure in the fluidised NiO nanoparticle catalyst allows ethyl radicals to desorb from the catalyst surface into the gas phase to initiate further gas-phase radical chain reactions. Therefore, the ethane-oxygen reaction catalysed by the fluidised NiO nanoparticles shows some typical behaviour of gas-phase reactions. In contrast, the rigid porous structure in the NiO/SiO(2) catalyst does not allow the radicals to desorb from catalyst surface into the bulk gas phase. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 174
页数:9
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