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作 者:夏鑫鑫 张宇 于洪洋 代明宇 汪艳艳 李锋[1] XIA Xinxin;ZHANG Yu;YU Hongyang;DAI Mingyu;WANG Yanyan;LI Feng(College of Chemistry and Chemical Engineering,Northeast Petroleum University,Daqing 163318,China;North Huajin Chemical Industries Group Corporation,Panjin 124021,China)
机构地区:[1]东北石油大学化学化工学院,黑龙江大庆163318 [2]北方华锦化学工业股份有限公司,辽宁盘锦124021
出 处:《化工科技》2023年第4期13-17,共5页Science & Technology in Chemical Industry
基 金:中央支持地方高校改革发展资金人才培养支持计划项目(2020GSP17);博士后研究员落户黑龙江科研基金项目(16190024)。
摘 要:以Cu基金属有机框架(MOF)负载RuCl 3,采用氢气还原法和真空碳热还原法制备Ru-Cu@C催化剂。以异丙醇为氢供体,研究Ru-Cu@C催化糠醛转移加氢制糠醇性能,考察催化剂制备方法、Ru负载量及催化反应条件的影响。结果表明,与氢气还原法相比,采用真空碳热还原法制备的Ru-Cu@C催化剂表现出更高的糠醛催化转移加氢活性和稳定性,T=453 K反应4 h,糠醛转化率93.7%,糠醇选择性98.2%,催化剂经5次循环使用后仍保持高的催化活性。Using Cu-based metal-organic frameworks loaded with RuCl 3,Ru-Cu@C catalysts were prepared by hydrogen reduction and vacuum carbothermic reduction,respectively.The catalytic transfer hydrogenation of furfural to furfuryl alcohol of the as-obtained catalysts was evaluated using isopropanol as hydrogen donor.The effects of preparation method,Ru loading,and catalytic reaction conditions were studied.The results showed that the vacuum carbothermic reduction-derived Ru-Cu@C catalyst shows higher catalytic activity and stability than the hydrogen reduction-derived catalyst.The furfural conversion was 93.7%and the furfuryl alcohol selectivity was 98.2%after 4 h at 453 K.The catalytic performance did not decrease significantly after reuse for five times.
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