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Multiphase reaction media including dense phase carbon dioxide and/or water: A case study for hydrogenation of phenol with a Pd/Al2O3 catalyst

机译:包含致密相二氧化碳和/或水的多相反应介质:以Pd / Al2O3催化剂氢化苯酚的案例研究

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摘要

Multiphase reaction media including dense phase CO2 and/or water were applied for a test reaction of hydrogenation of phenol with a Pd/Al2O3 catalyst. The features of these reaction media were clarified and the actions of dense phase CO2 and water were discussed. Different characterization methods (XPS, in situ high pressure FUR, ICP) were used to study (i) the surface of supported Pd particles that varied during the reaction, (ii) the competitive adsorption of phenol, water, and CO that was formed from H-2 and CO2 under pressurized conditions, and (iii) the leaching of active Pd species. Dense phase CO2 caused the deactivation of catalyst and it occurred more rapidly in the presence of both dense phase CO2 and water. In the system including water alone, the catalyst deactivation also happened but gradually. At the latter stage of reaction in this system, phenol was not consumed but cyclohexanone did transform to cyclohexanol. Those results may be explained by the leaching of Pd species and a structural change of supported Pd particles, resulting in a change in their adsorption behavior. The Pd leaching is more significant in acidic aqueous phase dissolving CO2 at high pressure. (C) 2013 Elsevier B.V. All rights reserved.
机译:将包括密相CO2和/或水的多相反应介质用于苯酚与Pd / Al2O3催化剂加氢的测试反应。阐明了这些反应介质的特征,并讨论了密相二氧化碳和水的作用。使用不同的表征方法(XPS,原位高压FUR,ICP)研究(i)反应期间负载的Pd颗粒的表面,(ii)苯酚,水和一氧化碳的竞争性吸附H-2和CO2在加压条件下,以及(iii)浸出活性Pd物质。密相CO2导致催化剂失活,并且在密相CO2和水同时存在时更迅速地发生。在仅包含水的系统中,催化剂失活也发生但逐渐发生。在该系统反应的后期,苯酚没有被消耗,但是环己酮确实转化为环己醇。可以通过Pd的浸出和负载的Pd颗粒的结构变化(导致其吸附行为发生变化)来解释这些结果。 Pd浸出在高压下溶解CO2的酸性水相中更为重要。 (C)2013 Elsevier B.V.保留所有权利。

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