首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Preparation of trimetallic Pt-Re-Ge/Al2O3 and Pt-Ir-Ge/Al2O3 naphtha reforming catalysts by surface redox reaction
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Preparation of trimetallic Pt-Re-Ge/Al2O3 and Pt-Ir-Ge/Al2O3 naphtha reforming catalysts by surface redox reaction

机译:表面氧化还原反应制备三金属Pt-Re-Ge / Al2O3和Pt-Ir-Ge / Al2O3石脑油重整催化剂

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Preparation of trimetallic Pt-Re-Ge/Al2O3 and Pt-Ir-Ge/Al2O3 naphtha reforming catalysts by means of a surface redox reaction (namely the catalytic reduction method), was studied by varying the concentration of Ge. The catalytic reduction method was chosen in order to favor the interaction of Ge with the active Pt-Re and Pt-Ir phases. The results shows that the deposition of Ge on the bimetallic catalysts does not seemingly depend on the nature of the metal phase (Pt-Ir or Pt-Re). The test reactions indicated that Ge addition modified the properties of both the metal and acid functions of the bimetallic catalysts. The modification of the acidity is due to the deposition of part of Ge on the support. The n-C-7 reforming results show that Pt-Re-Ge/Al2O3 and Pt-Ir-Ge/Al2O3 catalysts with low Ge contents (<= 0.3%) have similar catalytic performances (toluene yield, C-1-C-4 formation, coke deposit) as the presulfided bimetallic samples. This effect is attributed to an efficient passivation of hydrogenolytic activity at low Ge contents. At higher Ge contents a drastic decrease of the toluene yield is observed due to a strong poisoning of the metal phase and the formation of isolated Ge species. (c) 2006 Elsevier B.V. All rights reserved.
机译:通过改变Ge的浓度,研究了通过表面氧化还原反应制备三金属Pt-Re-Ge / Al2O3和Pt-Ir-Ge / Al2O3石脑油重整催化剂的方法。选择催化还原方法以促进Ge与活性Pt-Re和Pt-Ir相的相互作用。结果表明,Ge在双金属催化剂上的沉积似乎并不取决于金属相(Pt-Ir或Pt-Re)的性质。测试反应表明,Ge的添加改变了双金属催化剂的金属和酸官能团的性能。酸度的改变归因于部分Ge在载体上的沉积。 nC-7重整结果表明,低Ge含量(<= 0.3%)的Pt-Re-Ge / Al2O3和Pt-Ir-Ge / Al2O3催化剂具有相似的催化性能(甲苯收率,C-1-C-4形成) (焦炭沉积物)作为预硫化的双金属样品。该效应归因于在低Ge含量下氢钝化活性的有效钝化。在较高的Ge含量下,由于金属相的强烈中毒和离析的Ge物质的形成,观察到甲苯产率的急剧降低。 (c)2006 Elsevier B.V.保留所有权利。

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