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Hydrogenation of phenol with supported Rh catalysts in the presence of compressed CO2 : Its effects on reaction rate, product selectivity and catalyst life

机译:在压缩CO2存在下用负载型Rh催化剂催化苯酚加氢:对反应速率,产物选择性和催化剂寿命的影响

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摘要

Hydrogenation of phenol to cyclohexanone and cyclohexanol in/under compressed CO2 was examined using commercial Rh/C and Rh/Al2O3 catalysts to investigate the effects of CO2 pressurization on the total conversion and the product selectivity. Although the total rate of phenol hydrogenation with Rh/C was lowered by the presence of CO2, the selectivity to cyclohexanone was improved at high conversion levels > 70%. On the other hand, the activity of Rh/Al2O3 was completely lost in an early stage of reaction. The features of these multiphase catalytic hydrogenation reactions using compressed CO2 were studied in detail by phase behavior and solubility measurements, in situ high-pressure FTIR for molecular interactions of CO2 with reacting species and formation/adsorption of CO on the catalysts, and simulation of reaction kinetics using a simple model. The CO2 pressurization was shown to suppress the hydrogenation of cyclohexanone to cyclohexanol, improving the selectivity to cyclohexanone. The formation and adsorption of CO were observed for the two catalysts at high CO2 pressures in the presence of H2, which was one of important factors retarding the rate of hydrogenation in the presence of CO2. It was further indicated that the adsorption of CO on Rh/Al2O3 was strong and caused the complete loss of its activity.
机译:使用商业化的Rh / C和Rh / Al2O3催化剂检查了在压缩CO2中/压缩下苯酚加氢成环己酮和环己醇的作用,以研究CO2加压对总转化率和产物选择性的影响。尽管由于存在二氧化碳,降低了用Rh / C进行苯酚加氢的总速率,但在高转化率> 70%的情况下,对环己酮的选择性有所提高。另一方面,Rh / Al2O3的活性在反应的早期完全丧失。通过相行为和溶解度测量,原位高压FTIR研究CO2与反应物的分子相互作用以及CO在催化剂上的形成/吸附以及反应模拟,详细研究了压缩CO2的这些多相催化氢化反应的特征。动力学使用一个简单的模型。显示出CO 2加压抑制了环己酮氢化成环己醇,从而提高了对环己酮的选择性。在H2存在下,在高CO2压力下观察到两种催化剂的CO形成和吸附,这是阻碍CO2存在下氢化速率的重要因素之一。进一步表明,CO在Rh / Al2O3上的吸附很强,导致其活性完全丧失。

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