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Dehydrogenation of Ethylbenzene to Styrene with CO2 over TiO2-ZrO2 Bifunctional Catalyst

机译:TiO2-ZrO2双功能催化剂上CO2催化乙苯脱氢制苯乙烯

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摘要

In the dehydrogenation of ethylbenzene to styrene,CO2 could play a role as an oxidant to increase conversion of ethylbenzene and stability as well over TiO_2-ZrO2 mixed oxide catalysts,TiO2-ZrO2 catalysts were prepared by co-precipitation method and were characterized by BET surface area,bulk density,X-ray diffraction,temperature programmed desorption of NH3 and CO2.These catalysts were found to be X-ray amorphous with enhanced surface areas and acid-base properties both in number and strength when compared to the respective oxides (TiO2 and CO2).These catalysts were found to be highly active (> 50% conversion),selective (> 98%) and catalytically stable (10 h of time-on-stream) at 600 °C for the dehydrogenation of ethylbenzene to styrene.However,in the nitrogen stream,both activity and stability were rather lower than those in the stream with CO2.The TiO2-ZrO2 catalysts were catalytically superior to the simple oxide catalysts such as TiO2 and ZrO2.The synergistic effect of CO2 has clearly been observed in directing the product selectivity and prolonging catalytic activity.
机译:在乙苯脱氢成苯乙烯中,CO2可以起氧化剂的作用,以提高乙苯的转化率和稳定性,与TiO_2-ZrO2混合氧化物催化剂相比,采用共沉淀法制备了TiO2-ZrO2催化剂,并具有BET表面特征。面积,本体密度,X射线衍射,NH3和CO2的程序升温脱附。与相应的氧化物(TiO2)相比,这些催化剂是X射线无定形的,具有增加的表面积和酸碱性质(在数量和强度上)。发现这些催化剂在600°C下对乙苯脱氢为苯乙烯具有高活性(> 50%转化率),选择性(> 98%)和催化稳定(10 h的运行时间)。然而,在氮气流中,其活性和稳定性均低于含二氧化碳的流。TiO2-ZrO2催化剂在催化性能上优于简单的氧化物催化剂,例如TiO2和ZrO2。CO2的协同作用具有重要作用。在指导产物的选择性和延长催化活性方面都观察到了这一点。

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