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化学进展 2007, Vol. 19 Issue (05): 651-658 前一篇   后一篇

• 综述与评论 •

甘油催化氢解的研究与应用

冯建; 袁茂林; 陈华*; 李贤均   

  1. 四川大学化学学院有机金属络合催化研究所 绿色化学与技术教育部重点实验室 成都 610064
  • 收稿日期:2006-06-27 修回日期:2006-08-12 出版日期:2007-05-24 发布日期:2007-05-24
  • 通讯作者: 陈华

Studies and Applications of Catalytic Hydrogenolysis of Glycerol

Feng Jian;Yuan Maolin;Chen Hua*;Li Xianjun   

  1. Key Laboratory of Green Chemistry and Technology, Ministry of Education, Institute of Homogeneous Catalysis, College of Chemistry, Sichuan University, Chengdu 610064, China
  • Received:2006-06-27 Revised:2006-08-12 Online:2007-05-24 Published:2007-05-24
近年来由于生物柴油产业的快速发展,甘油作为其生产过程中的副产品大量生成,合理利用这些过剩的甘油将有助于增加整个生物柴油产业的经济效益。本文对近年来利用甘油为原料催化氢解合成二元醇(1,2-丙二醇、1,3-丙二醇和乙二醇)的研究进展进行了综述,介绍了甘油催化氢解的研究背景,着重讨论了甘油催化氢解生成二元醇的反应机理(包括脱水-加氢机理、脱氢-加氢机理和螯合机理)和甘油催化氢解在生产二元醇上的应用,并对甘油催化氢解的发展前景做了展望。
Because of the rapid development of biodiesel production by transesterification of vegetable oils and animal fats, large quantities of glycerol are formed as a reaction by-product. Seeking new utilization for the superfluous glycerol will improve the economy of the whole biodiesel production process. The studies of catalytic hydrogenolysis of glycerol have greatly increased in recent years, while no corresponding research has been reported in China. In this paper, the recent advances in catalytic hydrogenolysis of glycerol(1,2-propanediol,1,3-propanediol and ethylene glycol) are reviewed. The background of the studies of hydrogenolysis of glycerol is introduced. Then, emphases are focused on the reaction mechanisms (including the dehydration-hydrogenation mechanism,dehydrogenation-hydrogenation mechanism and chelation mechanism) and the application of catalytic hydrogenolysis of glycerol to glycols.The developing prospect of this research is also forecasted.

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[ 1 ] 闵恩泽(Min E Z) . 化学进展( Progress in Chemistry) , 2006 ,18(2/3) : 131 —141
[ 2 ] 闵恩泽(Min E Z) . 绿色化学技术( Green Chemistry Technology) . 南昌: 江西科学技术出版社(Nanchang :Jiangxi Science &Technology Press) , 2001. 1 —28
[ 3 ] Tundo P , Anastas P , Breen J , et al . Pure Appl . Chem. , 2000 ,72 : 1207 —1228
[ 4 ] Suppes G J , Dasari M A , Goff M J , et al . Appl . Catal . A:Gen. , 2004 , 257 : 213 —223
[ 5 ] Plank C , Lorbeer E. J . Chromatogr. A , 1995 , 697 : 461 —468
[ 6 ] Zartman W H , Adkins H. J . Am. Chem. Soc. , 1933 , 55 :4559 —4563
[ 7 ] Lenth C W, Dupuis R N. Ind. Eng. Chem. , 1945 , 37 :152 —157
[ 8 ] Kruse W M. US 3 935 284 , 1976
[ 9 ] Arena B J . US 4 380 679 , 1983
[10] Sirkar A K. US 4 380 678 , 1983
[11] Dubeck M, Knapp G G. US 4 476 331 , 1984
[12] Wright L W. US 3 965 199 , 1976
[13] Andrews M A , Klaeren S A. US 5 026 927 , 1991
[14] Schuster L , Himmele W. US 5 210 335 , 1993
[15] Casale B , Marini L. EP 0 510 238A1 , 1992
[16] Gubitosa G, Casale B. US 5 326 912 , 1994
[17] Gubitosa G, Casale B. US 5 354 914 , 1994
[18] Gubitosa G, Casale B. US 5 600 028 , 1997
[19] Chopade S P , Miller D J , Jackson J E , et al . US 6 291 725B1 ,2001
[20] Che T M. US 4 642 394 , 1987
[21] Dasari M A , Kiatsimkul P P , Suppes GJ , et al . Appl . Catal . A:Gen. , 2005 , 281 : 225 —231
[22] Montassier C , Menezo J C , Hoang L C , et al . J . Mol . Catal . ,1991 , 70 : 99 —110
[23] Chaminand J , Djakovitch L , Pinel C , et al . Green Chem. ,2004 , 6 : 359 —361
[24] Kusunoki Y, Miyazawa T , Tomishige K, et al . Catal . Commun. ,2005 , 6 : 645 —649
[25] Miyazawa T , Kusunoki Y, Tomishige K, et al . J . Catal . , 2006 ,240 : 213 —221
[26] Schlaf M, Ghosh P , Bullock R M, et al . Angew. Chem. Int .Ed. , 2001 , 40 : 3887 —3890
[27] Lahr D G, Shanks B H. J . Catal . , 2005 , 232 : 386 —394
[28] Lahr D G, Shanks B H. Ind. Eng. Chem. Res. , 2003 , 42 :5467 —5472
[29] Wang K Y, Hawley M C , Furney T D. Ind. Eng. Chem. Res. ,1995 , 34 : 3766 —3770
[30] Kuo YJ , Tatarchuk B J . J . Catal . , 1988 , 112 : 229 —249
[31] Kuo Y J , Cocco R A , Tatarchuk B J . J . Catal . , 1988 , 112 :250 —266
[32] Montassier C , Dumas J M, Granger P , et al . Appl . Catal . A:Gen. , 1995 , 121 : 231 —244
[33] 石英华(Shi Y H) . 沈阳化工( Shenyang Chemical Industry) ,1996 , 3 : 35 —37
[34] Celio L P , Maria W M, Bachman G W, et al . WO 9 744 302 ,1997
[35] Maria W M, Jorge R. WO 9 744 308 , 1997
[36] Casale B , Gomez A M. US 5 214 219 , 1993
[37] Casale B , Gomez A M. US 5 276 181 , 1994
[38] Fleckenstein T , Goebel G, Carduck F J . DE 4 302 464 , 1994
[39] Schuster L , Eggersdorfer M. US 5 616 817 , 1997
[40] Werpy T A , Frye J G, Zacher A H , et al . US 6 841 085B2 , 2005
[41] Perosa A , Tundo P. Ind. Eng. Chem. Res. , 2005 , 44 : 8535 —8537
[42] Montassier C , Giraud D , Barbier J , et al . Bull . Soc. Chim.Fr. , 1989 , 2 : 148 —155
[43] Runeberg J , Baiker A , Kijenski J . Appl . Catal . , 1985 , 17 :309 —319
[44] Montassier C , Giraud D , Barbier J . Stud. Surf . Sci . Catal . ,1988 , 41 : 165 —170
[45] 杨菊群(Yang J Q) , 王幸宜(Wang X Y) , 戚蕴石(Qi Y S) .石油化工(Petrochemical Technology) , 2002 , 31 : 943 —947
[46] 李吉春(Li J C) , 赵旭涛( Zhao X T) . 石油技术与应用(Petrochemical Technology and Application) , 2004 , 22 : 4 —11
[47] Haas T , Jaeger B , Weber R , et al . Appl . Catal . A: Gen. ,2005 , 280 : 83 —88
[48] Drent E , Jager W W. US 6 080 898 , 2000
[49] Haas T , Neher A , Arntz D , et al . US 5 426 249 , 1995
[50] Wang K Y, Hawley M C , DeAthos SJ . Ind. Eng. Chem. Res. ,2003 , 42 : 2913 —2923
[51] 崔小明(Cui X M) . 上海化工(Shanghai Chemical Industry) ,2004 , 11 : 43 —46
[52] 崔小明(Cui X M) . 上海化工(Shanghai Chemical Industry) ,2004 , 12 : 41 —44
[53] 朱培玉(Zhu P Y) , 李扬(Li Y) , 王永宏(Wang Y H) . 化工进展(Chemical Industry and Engineeting Progress) , 2002 , 21 :713 —717
[54] Tanikella M. EP 0 072 629 , 1983
[55] Tanikella M. US 4 404 411 , 1983
[56] Werpy T A , Frye J G, Zacher A H , et al . WO 03 035 582 , 2003
[57] Crabtree S P , Lawrence R C , Tuck M W, et al . Hydrocarbon Process , 2006 , 85 : 87 —92
[58] Chiu C W, Dasari M A , Suppes G J , et al . Ind. Eng. Chem.Res. , 2006 , 45 : 791 —795

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摘要

甘油催化氢解的研究与应用