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Catalytic behaviour of a bifunctional system for the one step synthesis of DME by CO2 hydrogenation

机译:CO2加氢一步合成DME的双功能体系的催化行为

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One-step CO2 hydrogenation reaction to dimethyl ether (DME) on a bifunctional system constituted by Cu-ZnO-ZrO2 (ZCZ) methanol synthesis catalyst and HZSM-5 zeolite was studied. The influence of the reactor configuration in terms of combination procedure of the admixed samples on activity, selectivity and DME yield has been evaluated. The results obtained at T_R = 513K, P_R = 3.0MPa and GHSV = 9000 NL g_(cat)~(-1) h~(-1) show a superior DME productivity (4.4 mmol kg_(zcz)~(-1) s~(-1)) using the bifunctional catalyst prepared by physical mixing. A combined effect of active sites located at metal/oxide(s)-acid interface was claimed as the main factor affecting the CO2 conversion and DME productivity. The strong surface acidity of ZCZ catalyst is not suitable to drive DME synthesis through a consecutive mechanism, while DME formation effectively proceeds on weak and medium acid sites of HZSM-5.
机译:研究了由Cu-ZnO-ZrO2(ZCZ)甲醇合成催化剂和HZSM-5沸石构成的双功能体系上的一步式CO2加氢制二甲醚(DME)。已经评估了反应器配置在混合样品的组合过程方面对活性,选择性和DME收率的影响。在T_R = 513K,P_R = 3.0MPa和GHSV = 9000 NL下获得的结果g_(cat)〜(-1)h〜(-1)显示出优异的DME生产率(4.4 mmol kg_(zcz)〜(-1)s 〜(-1))使用通过物理混合制备的双官能催化剂。声称位于金属/氧化物/酸-酸界面的活性部位的综合作用是影响CO2转化率和DME生产率的主要因素。 ZCZ催化剂的强表面酸度不适合通过连续机理驱动DME合成,而DME的形成则在HZSM-5的弱酸和中酸位点上有效地进行。

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