Raney Ni催化二亚糠基丙酮加氢制取长链烷烃前驱体的特性研究  

Catalytic performance of Raney Ni in the hydrogenation of di-furfural-acetone for producing long-chain alkane precursors

作　　者：黄晓明[1,2] 章青[1] 王铁军[1] 马隆龙[1] 张琦[1] 张兴华[1,2] 于玉肖[1,2] 左华亮[1,2] 刘建国[1,2] 杨勇[1,2] 

机构地区：[1]中国科学院广州能源研究所可再生能源与天然气水合物重点实验室,广东广州510640 [2]中国科学院大学,北京100049

出　　处：《燃料化学学报》2013年第1期79-84,共6页Journal of Fuel Chemistry and Technology

基　　金：国家高技术研究发展计划(863计划;2012AA101806);国家自然科学基金(51161140331);国家重点基础研究发展规划(973计划;2012CB215304)

摘　　要：采用Raney Ni为催化剂,考察了反应温度、压力、时间和溶剂对二亚糠基丙酮加氢制取长链烷烃前驱体催化性能的影响。结果表明,Raney Ni对二亚糠基丙酮具有很好的低温加氢性能,升高反应温度和压力均有利于加氢反应的进行,但过高的温度反而不利于加氢反应。在50℃和2.5 MPa下反应2 h,二亚糠基丙酮转化率达99.5%以上,饱和加氢产物的总选择性达到80.8%。此外,加氢中间产物的变化结果表明,二亚糠基丙酮的双键加氢容易程度为,烯键>呋喃环双键>C=O双键。Raney Ni在甲醇溶剂中的加氢性能明显高于在四氢呋喃、环己烷或水溶剂中的加氢性能。The hydrogenation of di-furfural-acetone for producing long-chain alkane precursors was carried out over Raney Ni catalyst; the effects of reaction temperature, pressure and time on the product distribution were investigated. The results indicated that Raney Ni exhibits excellent catalytic performance at low temperature. The hydrogenation can be enhanced by increasing temperature and pressure; at 50℃, 2. 5 MPa and after 2 h reaction, the di-furfural-acetone is completely converted with 80. 8% of the selectivity to the saturated hydrogenated products. However, excessive high temperature may be harmful to the hydrogenation. It was found that the hydrogenation activity towards three double bonds in di-furfural-acetone follows the order of ethylenic bond〉furan ring double bond〉C=O. Various solvents （water, methanol, tetrahydrofuran and cyclohexane） are also different in their effects on the catalytic performance; Raney Ni exhibits much higher hydrogenation activity in methanol than in other solvents.

关 键 词：二亚糠基丙酮 RANEY NI 加氢 长链烷烃 

分 类 号：TK6[动力工程及工程热物理—生物能]