Pt-Cu bimetallic catalysts obtained from layered double hydroxides by an anion-exchange route

被引:16
作者
Barrabes, N. [1 ]
Frare, A. [2 ]
Foettinger, K. [1 ]
Urakawa, A. [3 ]
Llorca, J. [4 ]
Rupprechter, G. [1 ]
Tichit, D. [2 ]
机构
[1] Vienna Univ Technol, Inst Mat Chem, A-1060 Vienna, Austria
[2] Inst Charles Gerhardt, CNRS UM2 ENSCM UM1, Equipe Mat Avances Catalyse & Sante, UMR 5253, F-34296 Montpellier 5, France
[3] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
[4] UPC, Inst Tecn Energet, ETSEIB, Barcelona 08028, Spain
关键词
Anionic-exchange; Hydrotalcite; Nitrate removal; Bimetallic catalyst; Citrate colloids; HYDROTALCITE-DERIVED CATALYSTS; THERMAL EVOLUTION; POROUS STRUCTURE; PARTICLE-SIZE; LDH COMPOUNDS; MIXED OXIDES; WATER; INTERCALATION; REDUCTION; NITRATE;
D O I
10.1016/j.clay.2012.07.011
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
Bimetallic Pt-Cu catalyst precursors have been prepared from NO3--Mg/Al layered double hydroxide (LDH) by anionic exchange with negatively charged copper hydroxy citrate colloids ([Cu(C6O7H3)(x)(OH)(y)(y(3x-1)-)) and [PtCl6](2-) species. Successive exchanges by varying the addition order of the two anionic species allowed removing NO3- almost completely and obtaining Cu/Pt molar ratios of 50.2 and 6.8 when Cu-containing colloids were introduced first (CuPt) or second (PtCu), respectively. After calcination and reduction treatments, the resulting materials were characterized by TPR and XPS analyses. Pt and Cu particles were homogeneously dispersed with the particle size of 2-7 nm and the portion of Cu present as Pt-Cu alloy was 48.9% (CuPt) and 69.8% (PtCu), showing remarkably enhanced alloy formation by the PtCu exchange order. Using this PtCu material, total conversion in nitrate hydrogenation reaction was achieved with higher selectivity toward nitrogen than those reported with bimetallic Pd-Cu catalysts prepared from LDH precursors by impregnation and co-precipitation routes. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 47 条
[1]   Catalytic reduction of nitrates in water on Pt promoted Cu hydrotalcite-derived catalysts: Effect of the Pt-Cu alloy formation [J].
Aristizabal, A. ;
Contreras, S. ;
Barrabes, N. ;
Llorca, J. ;
Tichit, D. ;
Medina, F. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 110 :58-70
[2]   Catalytic activity and characterization of Pt/calcined CuZnAl hydrotalcites in nitrate reduction reaction in water [J].
Aristizabal, A. ;
Kolafa, M. ;
Contreras, S. ;
Dominguez, M. ;
Llorca, J. ;
Barrabes, N. ;
Tichit, D. ;
Medina, F. .
CATALYSIS TODAY, 2011, 175 (01) :370-379
[3]   Pt-MgZnCuAl hydrotalcite-derived catalysts in the reduction of nitrates using continuous and batch reactors [J].
Barrabes, N. ;
Garrido, M. A. ;
Frare, A. ;
Monzon, A. ;
Tichit, D. .
CATALYSIS TODAY, 2011, 175 (01) :328-337
[4]   Catalytic nitrate removal from water, past, present and future perspectives [J].
Barrabes, Noelia ;
Sa, Jacinto .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 104 (1-2) :1-5
[5]   Performance of new Pt and Pt-Cu on hydrotalcite-derived materials for NOx storage/reduction [J].
Basile, F ;
Fornasari, G ;
Livi, M ;
Tinti, F ;
Trifirò, F ;
Vaccari, A .
TOPICS IN CATALYSIS, 2004, 30-1 (1-4) :223-227
[6]   Hydrotalcite-type precursors of active catalysts for hydrogen production [J].
Basile, F. ;
Benito, P. ;
Fornasari, G. ;
Vaccari, A. .
APPLIED CLAY SCIENCE, 2010, 48 (1-2) :250-259
[7]   Synthesis and thermal evolution of hydrotalcite-type compounds containing noble metals [J].
Basile, F ;
Fornasari, G ;
Gazzano, M ;
Vaccari, A .
APPLIED CLAY SCIENCE, 2000, 16 (3-4) :185-200
[8]   Intercalation of noble metal complexes in LDH compounds [J].
Beaudot, P ;
De Roy, ME ;
Besse, JP .
JOURNAL OF SOLID STATE CHEMISTRY, 2004, 177 (08) :2691-2698
[9]   Intercalation of platinum complex in LDH compounds [J].
Beaudot, P ;
De Roy, ME ;
Besse, JP .
JOURNAL OF SOLID STATE CHEMISTRY, 2001, 161 (02) :332-340
[10]   HYDROTALCITE-TYPE ANIONIC CLAYS: PREPARATION, PROPERTIES AND APPLICATIONS [J].
Cavani, F. ;
Trifiro, F. ;
Vaccari, A. .
CATALYSIS TODAY, 1991, 11 (02) :173-301