Catalytic transformation of glycerol on several metal systems supported on ZnO

被引:52
作者
Checa, Manuel [1 ]
Auneau, Florian [2 ]
Hidalgo-Carrillo, Jesus [1 ]
Marinas, Alberto [1 ]
Marinas, Jose M. [1 ]
Pinel, Catherine [2 ]
Urbano, Francisco J. [1 ]
机构
[1] Univ Cordoba, Fac Sci, E-14014 Cordoba, Spain
[2] CNRS UCBL, UMR 5256, IRCELYON, F-69626 Villeurbanne, France
关键词
Glycerol hydrogenolysis; Strong metal-support interaction (SMSI); Platinum; Rhodium; Palladium; Gold; 1,2-Propanediol (1,2-PDO); Lactic acid; Acetol; SELECTIVE HYDROGENATION; OXYGEN VACANCIES; AQUEOUS-SOLUTION; HYDROGENOLYSIS; CROTONALDEHYDE; OXIDATION; ALUMINA;
D O I
10.1016/j.cattod.2012.02.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Different metal systems consisting in platinum supported on several reducible supports (5% by weight) were synthesized through the deposition-precipitation technique and tested for glycerol hydrogenolysis. Interestingly, supports exhibiting the highest conversions were those with the greatest strong metal-support interaction (SMSI) effect, ZnO and SnO2, eventually forming alloys (Pt-Zn and Pt-Sn, respectively). ZnO was subsequently selected for further studies as support for Rh, Pt, Pd and Au and the resulting solids were tested again for glycerol catalytic transformation under reductive or inert atmosphere at 453 K. Under similar reaction conditions, glycerol conversion order followed the sequence Pt > Rh >> Pd >> Au. Moreover, the solids reduced at 473 K were more active than those activated at 673 K, which evidences the detrimental effect of the increase in metal particle size and/or alloy formation on the catalytic performance. Quite high yields to lactic acid were achieved in a basic medium (e. g. 68% for Rh/ZnO-473 under H-2) whereas yield to 1,2-PDO was more modest (26% for Rh/ZnO-673 under similar reaction conditions). (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:91 / 100
页数:10
相关论文
共 33 条
[1]  
Abdel-Rahman MA, 2011, J BIOTECHNOL, V156, P286, DOI [10.1016/j.jbiotec.2011.06.017 , 10.1016/j.jbiotec.2011.06.017]
[2]   An emergent catalytic material: Pt/ZnO catalyst for selective hydrogenation of crotonaldehyde [J].
Ammari, F ;
Lamotte, J ;
Touroude, R .
JOURNAL OF CATALYSIS, 2004, 221 (01) :32-42
[3]   Effect of the redox treatment of Pt/TiO2 system on its photocatalytic behaviour in the gas phase selective photooxidation of propan-2-ol [J].
Aramendia, M. A. ;
Colmenares, J. C. ;
Marinas, A. ;
Marinas, J. M. ;
Moreno, J. M. ;
Navio, J. A. ;
Urbano, F. J. .
CATALYSIS TODAY, 2007, 128 (3-4) :235-244
[4]  
Auneau F., 2011, THESIS U CB LYON 1 F, P134
[5]   On the role of the atmosphere in the catalytic glycerol transformation over iridium-based catalysts [J].
Auneau, Florian ;
Noel, Sebastien ;
Aubert, Guillaume ;
Besson, Michele ;
Djakovitch, Laurent ;
Pinel, Catherine .
CATALYSIS COMMUNICATIONS, 2011, 16 (01) :144-149
[6]   Influence of solid acids as co-catalysts on glycerol hydrogenolysis to propylene glycol over Ru/C catalysts [J].
Balaraju, M. ;
Rekha, V. ;
Prasad, P. S. Sai ;
Devi, B. L. A. Prabhavathi ;
Prasad, R. B. N. ;
Lingaiah, N. .
APPLIED CATALYSIS A-GENERAL, 2009, 354 (1-2) :82-87
[7]   Some contributions of electron microscopy to the characterisation of the strong metal-support interaction effect [J].
Bernal, S ;
Calvino, JJ ;
Cauqui, MA ;
Gatica, JM ;
Cartes, CL ;
Omil, JAP ;
Pintado, JM .
CATALYSIS TODAY, 2003, 77 (04) :385-406
[8]   Glycerol hydrogenolysis on heterogeneous catalysts [J].
Chaminand, J ;
Djakovitch, L ;
Gallezot, P ;
Marion, P ;
Pinel, C ;
Rosier, C .
GREEN CHEMISTRY, 2004, 6 (08) :359-361
[9]   High performances of Pt/ZnO catalysts in selective hydrogenation of crotonaldehyde [J].
Consonni, M ;
Jokic, D ;
Murzin, DY ;
Touroude, R .
JOURNAL OF CATALYSIS, 1999, 188 (01) :165-175
[10]   The activation of a Pd/γ-alumina catalyst during methane combustion:: investigation of the phenomenon and of potential causes [J].
Demoulin, O ;
Navez, M ;
Ruiz, P .
CATALYSIS LETTERS, 2005, 103 (1-2) :149-153