In situ generated palladium nanoparticles in imidazolium-based ionic liquids: a versatile medium for an efficient and selective partial biodiesel hydrogenation

被引:25
作者
Carvalho, Myller S. [1 ]
Lacerda, Raisa A. [1 ]
Leao, Joao P. B. [1 ]
Scholten, Jackson D. [2 ]
Neto, Brenno A. D. [3 ]
Suarez, Paulo A. Z. [1 ]
机构
[1] Univ Brasilia, Inst Quim, Lab Mat & Combustiveis, INCT CATALISE, Brasilia, DF, Brazil
[2] Chem Inst UFRGS, Lab Mol Catalysis, Porto Alegre, RS, Brazil
[3] Univ Brasilia, Inst Quim, Lab Med & Technol Chem, INCT CATALISE, Brasilia, DF, Brazil
关键词
2-PHASE CATALYTIC-HYDROGENATION; SOYBEAN OIL; METHYL-ESTERS; MOLTEN-SALTS; 1,3-BUTADIENE; TETRAFLUOROBORATE; STABILITY; COMPLEXES; OXIDATION; OLEFINS;
D O I
10.1039/c0cy00028k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An important drawback to be overcome in biodiesel technology is its low oxidative stability. One approach to improve the oxidative stability of soybean oil biodiesel is the partial hydrogenation of double bonds. In the current work, an efficient two-phase catalytic system using palladium acetate dissolved in BMI center dot BF4 ionic liquid to an in situ generation of palladium nanoparticles was developed in order to promote a selective hydrogenation reaction. Upon using this catalytic system it was possible to partially hydrogenate biodiesel into mono-hydrogenated compounds avoiding the formation of saturated compounds. The nanoparticulate system was compared with the traditional heterogeneous Pd/C system and gave far higher selectivity. It was possible to recover and reuse the ionic phase containing the catalyst up to three times without significant loss in its catalytic performance. Indeed, atomic absorption spectroscopy showed an excellent reclaim of the catalyst, which stayed in the ionic phase. Several parameters, such as temperature, hydrogen pressure, metal concentration and reaction time, were also evaluated.
引用
收藏
页码:480 / 488
页数:9
相关论文
共 44 条
[1]   New multi-phase catalytic systems based on tin compounds active for vegetable oil transesterificaton reaction [J].
Abreu, FR ;
Alves, MB ;
Macêdo, CCS ;
Zara, LF ;
Suarez, PAZ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 227 (1-2) :263-267
[2]   Utilization of metal complexes as catalysts in the transesterification of Brazilian vegetable oils with different alcohols [J].
Abreu, FR ;
Lima, DG ;
Hamú, EH ;
Wolf, C ;
Suarez, PAZ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 209 (1-2) :29-33
[3]   New metal catalysts for soybean oil transesterification [J].
Abreu, FR ;
Lima, DG ;
Hamú, EH ;
Einloft, S ;
Rubim, JC ;
Suarez, PAZ .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 2003, 80 (06) :601-604
[4]  
*AOCS, 1999, 12B92 CD AOCS
[5]  
*AOCS, 1999, 125 CD AOCS
[6]  
CARVALHO MS, UNPUB
[7]   A simple and practical method for the preparation and purity determination of halide-free imidazolium ionic liquids [J].
Cassol, CC ;
Ebeling, G ;
Ferrera, B ;
Dupont, J .
ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (1-2) :243-248
[8]  
Chauvin Y, 1995, ANGEW CHEM INT EDIT, V34, P2698
[9]   HYDROGENATION OF EDIBLE OILS [J].
COENEN, JWE .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1976, 53 (06) :382-389
[10]   Selective hydrogenation of 1,3-butadiene by transition metal compounds immobilized in 1-butyl-3-methyl imidazolium room temperature ionic liquids [J].
Consorti, CS ;
Umpierre, AP ;
de Souza, RF ;
Dupont, J ;
Suarez, PAZ .
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2003, 14 (03) :401-405