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Catalytic transfer hydrogenation/hydrogenolysis of guaiacol to cyclohexane over bimetallic RuRe/C catalysts

机译:双金属RuRe / C催化剂上愈创木酚催化转移加氢/氢解制环己烷

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摘要

The hydrodeoxygenation of lignin monomer guaiacol via catalytic transfer hydrogenation was studied with 2-propanol as a hydrogen donor and Ru-based catalysts. Guaiacol was mainly converted into a partially deoxygenated product, cyclohexanol (>70% selectivity), over Ru/C catalysts with the hydrogen produced in-situ from 2-propanol. An addition of Re to Ru/C catalysts significantly enhanced the rate of C-O hydrogenolysis, resulting in the complete deoxygenation to cyclohexane (similar to 60% selectivity). The remarkable deoxygenation ability of the bimetallic RuRe/C catalyst is attributed to its bifunctional characteristic, by which Ru catalyzes the hydrogenation-hydrogenolysis of guaiacol and Re provides acid sites to promote cyclohexane production via hydrogenolysis. (C) 2016 Elsevier B.V. All rights reserved.
机译:研究了木质素单体愈创木酚通过催化转移加氢的加氢脱氧反应,以2-丙醇为氢供体和Ru基催化剂为研究对象。愈创木酚在Ru / C催化剂上主要由2-丙醇原位产生的氢转化成部分脱氧的产物环己醇(选择性> 70%)。向Ru / C催化剂中添加Re可以显着提高C-O氢解的速率,从而使环己烷完全脱氧(选择性接近60%)。双金属RuRe / C催化剂的卓越脱氧能力归因于其双功能特性,其中Ru催化了愈创木酚的氢化加氢分解反应,而Re提供了酸点,通过氢解作用促进了环己烷的生产。 (C)2016 Elsevier B.V.保留所有权利。

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