Covalent Triazine Framework as Catalytic Support for Liquid Phase Reaction

被引:509
作者
Chan-Thaw, Carine E. [1 ]
Villa, Alberto [2 ]
Katekomol, Phisan [1 ]
Su, Dangsheng [3 ]
Thomas, Arne [1 ]
Prati, Laura [2 ]
机构
[1] Tech Univ Berlin, D-10587 Berlin, Germany
[2] Univ Milan, Dipartimento Chim Inorgan Met Organ & Analit, I-20133 Milan, Italy
[3] Max Planck Gesell, Fritz Haber Inst, Dept Inorgan Chem, D-14195 Berlin, Germany
关键词
Porous polymer framework; palladium; liquid phase oxidation; glycerol; DOPED CARBON NANOTUBES; SELECTIVE OXIDATION; GLYCEROL; PALLADIUM; POLYMERS; MOF-5;
D O I
10.1021/nl904082k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An important goal in the preparation of highly active supported metal particles is the enhancement of the metal support interaction, providing a more stable catalyst, especially for liquid phase reactions as the leaching and reconstruction of the active phase causes deactivation. In this work, a covalent triazine framework (CTF) as support for Pd nanoparticles is compared to activated carbon (AC), the typical support used in liquid phase reactions. The results indicate that the presence of the N-heterocyclic moieties on the surface of the frameworks is beneficial for improving the stability of Pd nanoparticles during the liquid phase glycerol oxidation. Pd/CTF showed better activity and in particular better stability when compared to Pd supported on activated carbon (AC).
引用
收藏
页码:537 / 541
页数:5
相关论文
共 34 条
[1]   N-doped carbon nanotubes for liquid-phase C=C bond hydrogenation [J].
Amadou, Julien ;
Chizari, Kambiz ;
Houlle, Matthieu ;
Janowska, Izabela ;
Ersen, Ovidiu ;
Begin, Dominique ;
Pham-Huu, Cuong .
CATALYSIS TODAY, 2008, 138 (1-2) :62-68
[2]   Selective oxidation of glycerol to glyceric acid using a gold catalyst in aqueous sodium hydroxide [J].
Carrettin, S ;
McMorn, P ;
Johnston, P ;
Griffin, K ;
Hutchings, GJ .
CHEMICAL COMMUNICATIONS, 2002, (07) :696-697
[3]  
DEMIRELGULEN S, 2005, CATAL TODAY, V166, P102
[4]   Effect of particle size on monometallic and bimetallic (Au,Pd)/C on the liquid phase oxidation of glycerol [J].
Dimitratos, N ;
Lopez-Sanchez, JA ;
Lennon, D ;
Porta, F ;
Prati, L ;
Villa, A .
CATALYSIS LETTERS, 2006, 108 (3-4) :147-153
[5]   Metal-Organic Frameworks: Opportunities for Catalysis [J].
Farrusseng, David ;
Aguado, Sonia ;
Pinel, Catherine .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (41) :7502-7513
[6]   Noble-metal-catalysed aqueous alcohol oxidation: reaction start-up and catalyst deactivation and reactivation [J].
Gangwal, VR ;
van der Schaaf, J ;
Kuster, BFM ;
Schouten, JC .
JOURNAL OF CATALYSIS, 2005, 232 (02) :432-443
[7]   Amino-based metal-organic frameworks as stable, highly active basic catalysts [J].
Gascon, Jorge ;
Aktay, Ugur ;
Hernandez-Alonso, Maria D. ;
van Klink, Gerard P. M. ;
Kapteijn, Freek .
JOURNAL OF CATALYSIS, 2009, 261 (01) :75-87
[8]   Metal@MOF:: Loading of highly porous coordination polymers host lattices by metal organic chemical vapor deposition [J].
Hermes, S ;
Schröter, MK ;
Schmid, R ;
Khodeir, L ;
Muhler, M ;
Tissler, A ;
Fischer, RW ;
Fischer, RA .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (38) :6237-6241
[9]   High-density attachment of gold nanoparticles on functionalized multiwalled carbon nanotubes using ion exchange [J].
Hou, Xianming ;
Wang, Lixia ;
Zhou, Feng ;
Wang, Fen .
CARBON, 2009, 47 (05) :1209-1213
[10]   New approaches to designing selective oxidation catalysts: Au/C a versatile catalyst [J].
Hutchings, Graham J. ;
Carrettin, Silvio ;
Landon, Philip ;
Edwards, Jennifer K. ;
Enache, Dan ;
Knight, David W. ;
Xu, Yi-Jin ;
Carley, Albert F. .
TOPICS IN CATALYSIS, 2006, 38 (04) :223-230