Reducibility of ruthenium in relation with zeolite structure

被引:40
作者
Pârvulescu, VI
Coman, S
Palade, P
Macovei, D
Teodorescu, CM
Filoti, G
Molina, R
Poncelet, G
Wagner, FE
机构
[1] Univ Bucharest, Fac Chem, Dept Chem Technol & Catalysis, Bucharest 70346, Romania
[2] Natl Inst Mat Phys, Bucharest 76900, Romania
[3] Univ Catholique Louvain, Unite Catalyse & Chim Mat Divises, B-1348 Louvain, Belgium
[4] Tech Univ Munich, Dept Phys E 15, D-85747 Munich, Germany
关键词
Ru-zeolite; EXAFS; Mossbauer spectroscopy; XPS; H-2; chemisorption; H-2-TPR;
D O I
10.1016/S0169-4332(98)00619-9
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
Ru-zeolites prepared via deposition of aqueous solution of ruthenium chloride on X, L, ZSM-5 and APO-54 were investigated. The impregnated solids were characterized by the following techniques: N-2 sorption, H-2 chemisorption, TPR, XRD, XPS, EXAFS and Mossbauer spectroscopy. It was found that deposition of Ru is influenced by the pore structure and the chemical composition of the supports, in particular the concentration and strength of the protonic sites, with the formation of the different species. The packing of Ru as well as the degree of the reduction and the metal particle size are different according to the penetration depth of the metal and the nature of the zeolite. The amount of chlorine possibly remaining as adatoms of Ru is very low or inexistent. In calcined and reduced catalysts no chloride peak could be evidenced by XPS. The experiments confirmed that the use of large amounts of Ru chloride precursor leads to rather large metal particles. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:164 / 176
页数:13
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