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作 者:徐龙伢[1] 王清遐[1] 徐奕德[1] 王开立[1] 杨力[1] 王德宝[1]
机构地区:[1]中国科学院大连化学物理研究所
出 处:《天然气化工—C1化学与化工》1996年第6期33-36,共4页Natural Gas Chemical Industry
基 金:国家"八.五"重点科技攻关课题
摘 要:对K-Fe-MnO/Silicalite-2催化剂积炭及烧炭的差热与热重分析结果表明,在CO加氢反应过程中催化剂表面可形成两种类型的积炭,其中Ⅰ型炭有利于提高CO加氢制低碳烯烃的选择性,而Ⅱ型炭则不能。研究结果还表明,K-Fe-MnO/Silicalite-2催化剂经再生后可恢复其新鲜态催化剂性能。在单管扩大试验中,反应器入口高温区催化剂表面容易形成Ⅰ型和Ⅱ型积炭,而恒温区催化剂表面只有Ⅰ型积炭。he differential thermal and thermo gravimetric analyses of K Fe MnO/silicalite 2 catalyst carbon deposit and carbon burning show that two types of carbon deposit may be formed on the catalyst surface during CO hydrogenation reaction, in which type I carbon deposit is advantagous to increase light olefins selectivity in CO hydrogenation, but type Ⅱ carbon deposit is not. The analytic results also show that K Fe MnO/silicalite 2 catalyst can be restored to its fresh state catalytic properties after regeneration. In the single tube scaleup tests, type Ⅰ and Ⅱ carbon deposits can easily be formed on the catalyst surface at the high temperature zone of the reactor inlet, and only type I carbon deposit is formed on the catalyst surface at the constant temperature zone, which will cause the displacement of the highest temperature zone in catalyst bed.
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