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作 者:迟亚武[1] 梁东白[1] 徐长海[1] 林培滋[1] 罗洪原[1] 林励吾[1]
机构地区:[1]中国科学院大连化学物理研究所
出 处:《燃料化学学报》1997年第2期157-161,共5页Journal of Fuel Chemistry and Technology
摘 要:在超细CuO/ZnO/SiO2催化剂体系上,对比研究了CO2和CO加氢性能,并就CO2加氢的反应机理进行了探讨。考察了接触时间和反应压力对CO2加氢的主要产物甲醇和CO分布的影响。结果表明,CO2加氢生成甲醇和CO是平行反应,生成的甲醇直接来源于CO2本身,没有经历CO中间物种,而且生成的CO能够适当地进一步加氢生成甲醇。在超细CuO/ZnO/SiO2催化剂体系的CO加氢反应主要产物是二甲醚和甲醇,这进一步支持上述反应机理。在488~568K反应温度范围内,超细CuO/ZnO/SiO2催化剂对CO2加氢的催化活性高于对CO加氢的活性。The hydrogenation of both CO 2 and CO were carried out on the ultrafine CuO/ZnO/SiO 2 catalysts prepared by solgel method and the reaction mechanism of hydrogenation of CO 2 was discussed The effects of contact time and reaction pressure from 1 0 ̄4 0MPa on the product distribution of CO 2 hydrogenation were investigated to clarify the reaction mechanism The main products of hydrogenation of CO 2 were methanol and CO, while dimethyl ether and methanol were the main products of hydrogenation of CO Our studies confirmed that the methanol from hydrogenation of CO 2 came directly from CO 2 rather than from CO, and the formation of methanol and CO from CO 2 were parallel reactions, moreover a suitable amount of CO formed from CO 2 could turn into methanol The comparative result of hydrogenation of CO further supported above mechanism and the ultrafine CuO/ZnO/SiO 2 catalysts showed higher activity to hydrogenation of CO 2 than to hydrogenation of CO in 488568K
分 类 号:O621.254.2[理学—有机化学] O643.36[理学—化学]
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