Catalytic and structural properties of ruthenium bimetallic catalysts: Preparation and characterization

Q4 Chemical Engineering 分子催化 Pub Date : 1994-08-12 DOI:10.1016/0304-5102(94)85006-2
Bernard Coq ∗ , Eleanor Crabb , Mayukh Warawdekar , Geoffrey C. Bond , Joop C. Slaa , Signorino Galvagno , Lucina Mercadante , Joaquin Garcia Ruiz , Maria Conception Sanchez Sierra
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引用次数: 40

Abstract

In the framework of an EC Stimulation Action Programme, alumina-supported mono- and bimetallic Ru, RuGe, RuSn and RuPb catalysts have been prepared from both organic and inorganic precursors. Herein are presented some basic properties of these materials obtained by TPR and TPO experiments, H2 and CO chemisorption, TEM examination, XPS and EXAFS studies. The use of organic precursors led to very small Ru particles, with a coordination number between Ru atoms of 4.35 (Ru0-Ru0+Ru0-Ruδ+). The size of the metallic particles was not modified by adding Ge, Sn or Pb by the controlled surface reaction technique. In very small aggregates, some Ru atoms (10–15%) remained partially oxidised even after reduction at 623 K in flowing hydrogen. During the coimpregnation of alumina with inorganic precursors, the modifier played the role of a nucleation center for Ru, thus allowing small particles to be formed. We believe that CO could modify the surface composition of small bimetallic RuGe particles during the chemisorption.

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钌双金属催化剂的催化和结构性能:制备和表征
在EC刺激行动方案的框架内,用有机和无机前体制备了氧化铝支持的单金属和双金属Ru、RuGe、RuSn和RuPb催化剂。本文介绍了通过TPR和TPO实验、H2和CO化学吸附、TEM、XPS和EXAFS研究获得的这些材料的一些基本性能。有机前驱体的使用使Ru颗粒非常小,Ru原子之间的配位数为4.35 (Ru0-Ru0+Ru0-Ruδ+)。通过控制表面反应技术,添加Ge、Sn或Pb均未改变金属颗粒的尺寸。在非常小的团聚体中,一些Ru原子(10-15%)即使在623 K的流动氢中还原后仍部分氧化。在氧化铝与无机前驱体共浸渍过程中,改性剂对Ru起到了成核中心的作用,从而形成了小颗粒。我们认为CO可以在化学吸附过程中改变小双金属RuGe颗粒的表面组成。
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分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
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0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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