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作 者:徐龙伢[1] 王清遐[1] 王开立[1] 王德室 杨力[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3期30-33,共4页Natural Gas Chemical Industry
基 金:国家"八五"重点科技攻关课题
摘 要:将小试开发成功的K-Fe-MnO/Silicalite-2催化剂进行了1.8L的单管扩大试验,采用强制盐浴循环加热及导热,可有效控制CO加氢的强放热效应,使催化剂床层温差控制在20℃以内,取得很好的效果,成功地进行了合成气制低碳烯烃的单管扩大试验,K-Fe-MnO/Silicalite-2催化剂的CO加氢制低碳烯烃性能可达到并超过小试结果,表明控制催化剂床层温差是确保合成气直接制取低碳烯烃单管扩大试验的关键。此外,根据催化剂床层高温区轴向位移的速度可推测催化剂的单程寿命。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.
分 类 号:TQ221.21[化学工程—有机化工] TE665.3[石油与天然气工程—油气加工工程]
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