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Kinetic study of the selective hydrogenation of styrene over a Pd egg-shell composite catalyst

机译:Pd蛋壳复合催化剂上苯乙烯选择性加氢的动力学研究

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摘要

This is a study on the kinetics of the liquid-phase hydrogenation of styrene to ethylbenzene over a catalyst of palladium supported on an inorganic–organic composite. This support has a better mechanical resistance than other commercial supports, e.g. alumina, and yields catalysts with egg-shell structure and a very thin active Pd layer. Catalytic tests were carried out in a batch reactor by varying temperature, total pressure and styrene initial concentration between 353–393 K, 10–30 bar, and 0.26–0.60 mol L−1. Kinetic models were developed on the assumptions of dissociative hydrogen chemisorption and non-negligible adsorption of hydrogen and styrene. Final chemical reaction expressions useful for reactor design were obtained. The models that best fitted the experimental data were those ones that considered the surface reaction as the limiting step. In this sense, a two-step Horiuti–Polanyi working mechanism with half hydrogenation intermediates gave the best fit of the experimental data. The heats of adsorption of styrene and ethylbenzene were also estimated.
机译:这是对负载在无机-有机复合材料上的钯催化剂上苯乙烯液相氢化为乙苯的动力学的研究。该支撑件具有比其他商业支撑件例如更好的机械抗性。氧化铝,并产生具有蛋壳结构和非常薄的活性Pd层的催化剂。在间歇反应器中通过在353–393 K,10–30 bar和0.26-0.60 mol L-1之间变化温度,总压力和苯乙烯初始浓度进行催化测试。动力学模型的建立是基于氢和苯乙烯的离解氢化学吸附和不可忽略的吸附。获得了对反应器设计有用的最终化学反应表达式。最适合实验数据的模型是那些将表面反应视为限制步骤的模型。从这个意义上讲,具有半氢化中间体的两步Horiuti-Polanyi工作机理最适合实验数据。还估计了苯乙烯和乙苯的吸附热。

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