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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
引用本文:黄晓明,章青,王铁军,马隆龙,张琦,张兴华,于玉肖,左华亮,刘建国,杨勇. 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[J]. 燃料化学学报, 2013, 41(1): 79-84
作者姓名:黄晓明  章青  王铁军  马隆龙  张琦  张兴华  于玉肖  左华亮  刘建国  杨勇
作者单位:1. Key Laboratory of Renewable Energy and Gas Hydrate, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China;2. University of Chinese Academy of Sciences, Beijing 100049, China
基金项目: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。

关 键 词:二亚糠基丙酮  Raney Ni  加氢  长链烷烃  
收稿时间:2012-05-29

Catalytic performance of Raney Ni in the hydrogenation of di-furfural-acetone for producing long-chain alkane precursors
HUANG Xiao-ming,ZHANG Qing,WANG Tie-jun,MA Long-long,ZHANG Qi,ZHANG Xing-hua,YU Yu-xiao,ZUO Hua-liang,LIU Jian-guo,YANG Yong. Catalytic performance of Raney Ni in the hydrogenation of di-furfural-acetone for producing long-chain alkane precursors[J]. Journal of Fuel Chemistry and Technology, 2013, 41(1): 79-84
Authors:HUANG Xiao-ming  ZHANG Qing  WANG Tie-jun  MA Long-long  ZHANG Qi  ZHANG Xing-hua  YU Yu-xiao  ZUO Hua-liang  LIU Jian-guo  YANG Yong
Affiliation:1,2(1.Key Laboratory of Renewable Energy and Gas Hydrate,Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences,Guangzhou 510640,China; 2.University of Chinese Academy of Sciences,Beijing 100049,China)
Abstract: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.
Keywords:di-furfural-acetone  Raney Ni  hydrogenation  long-chain alkane  
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