Gas phase catalysis by metal nanoparticles in nanoporous alumina membranes

被引:23
作者
Kormann, HP
Schmid, G [1 ]
Pelzer, K
Philippot, K
Chaudret, B
机构
[1] Univ Duisburg Gesamthsch, Inst Anorgan Chem, D-45117 Essen, Germany
[2] CNRS, Chim Coordinat Lab, Toulouse, France
来源
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE | 2004年 / 630卷 / 12期
关键词
gas phase catalysis; palladium nanoparticles; ruthenium nanoparticles; hydrogenation; oxidation; 1,3-butadiene; carbon monoxide; nanoporous alumina membranes;
D O I
10.1002/zaac.200400192
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Nanoporous alumina membranes, loaded with palladium and ruthenium nanoparticles of various size, were used for gas phase hydrogenation of 1,3-butadiene and for oxidation of carbon monoxide, respectively. Those membranes contain 10(9) - 10(11) pores per cm(2), all running perpendicular to the surface. Membrane discs of 20 mm in diameter and only 60 mum thick, incorporated in a reactor in which the reactants can be pumped in a closed circuit through the pores, turned out to very actively catalyze hydrogenation of butadiene (Pd) and oxidation of CO (Ru). The activity of the Pd catalysts depends characteristically on the particles size, the gas flow, and of the educts ratio. As could be expected, larger particles are less active than smaller ones, whereas increasing gas flows in case of hydrogenation accelerates the reactions. Excessive hydrogen reduces selectivity with respect to the various butenes, but favours formation of butane.
引用
收藏
页码:1913 / 1918
页数:6
相关论文
共 29 条
[1]   TURNOVER RATES IN HETEROGENEOUS CATALYSIS [J].
BOUDART, M .
CHEMICAL REVIEWS, 1995, 95 (03) :661-666
[2]  
BRADLEY JS, 2004, NANOPARTICLES THEORY
[3]  
Braunstein P, 2000, CHEM-EUR J, V6, P4637, DOI 10.1002/1521-3765(20001215)6:24<4637::AID-CHEM4637>3.0.CO
[4]  
2-A
[5]   Size dependence of the CO monolayer oxidation on nanosized Pt particles supported on gold [J].
Friedrich, KA ;
Henglein, F ;
Stimming, U ;
Unkauf, W .
ELECTROCHIMICA ACTA, 2000, 45 (20) :3283-3293
[6]   Preparation of supported gold catalysts for low-temperature CO oxidation via "size-controlled" gold colloids [J].
Grunwaldt, JD ;
Kiener, C ;
Wögerbauer, C ;
Baiker, A .
JOURNAL OF CATALYSIS, 1999, 181 (02) :223-232
[7]   Gold/titania interfaces and their role in carbon monoxide oxidation [J].
Grunwaldt, JD ;
Baiker, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (06) :1002-1012
[8]   Comparative study of Au/TiO2 and Au/ZrO2 catalysts for low-temperature CO oxidation [J].
Grunwaldt, JD ;
Maciejewski, M ;
Becker, OS ;
Fabrizioli, P ;
Baiker, A .
JOURNAL OF CATALYSIS, 1999, 186 (02) :458-469
[9]  
Hanaoka TA, 1998, APPL ORGANOMET CHEM, V12, P367, DOI 10.1002/(SICI)1099-0739(199805)12:5<367::AID-AOC732>3.3.CO
[10]  
2-P