Metal–support interactions in Pt/Al2O3 and Pd/Al2O3 catalysts for CO oxidation

煅烧 催化作用 铂金 高分辨率透射电子显微镜 材料科学 X射线光电子能谱 催化剂载体 金属 化学工程 结块 无机化学 化学 纳米技术 冶金 透射电子显微镜 复合材料 工程类 生物化学
作者
А. С. Иванова,Elena M. Slavinskaya,R. V. Gulyaev,В. И. Зайковский,О. А. Стонкус,И. Г. Данилова,L. M. Plyasova,I. A. Polukhina,A. I. Boronin
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:97 (1-2): 57-71 被引量:349
标识
DOI:10.1016/j.apcatb.2010.03.024
摘要

Platinum and palladium catalysts supported on γ-Al2O3 were studied by XRD, UV–vis DRS, HRTEM, TPR-H2, XPS together with measurements of their catalytic properties. The properties of the catalysts denoted as Pt(Pd)/Al2O3(X)-Y (X—the calcination temperature of support, °C; Y—the calcination temperature of catalyst, °C) were studied as a function of the temperatures used for calcination of the support and/or the catalyst in oxygen or in a reaction mixture of CO + O2. It was found that the deposition of Pt or Pd on γ-Al2O3 did not alter the structure of the support. Two types of the Pt and Pd particles were typically present on the γ-Al2O3 surface: individual particles with dimensions of 1.5–3 nm and agglomerates about 100 nm in size. In the catalysts calcined at relatively low temperatures (Pt/Al2O3(550)-450), platinum was present in the form of metal clusters. However, in the Pd/Al2O3(550)-450 catalyst, the palladium particles were almost completely decorated with a thin layer of an aluminate phase. These structures are not reduced in hydrogen in the temperature range of −15 to 450 °C, and are stable to treatment in a reaction mixture of CO + O2. Pd deposition on the γ-Al2O3-800 support was found to result in stabilization of the active component in two main forms, Pdo and PdO, with varying degrees of interaction due to the decoration effect. Calcination at the low temperature of 550 °C led to the formation of a so-called “core–shell structure”, where a palladium metal core is covered with a thin shell of an aluminate phase. Depending on the calcination temperature of the catalyst in the range of 450–1000 °C, the morphological form of the active component was converted from the “core-shell” state to a state consisting of two phases, Pdo and PdO, with a gradual decrease of the Pdo/PdO ratio, weakening the interaction with the support and the growth of palladium particles. Under the action of the reaction mixture, the Pd/Al2O3(800)-(450,600,800,1000) catalysts underwent changes in the Pdo/PdO ratio, which regulates the light-off temperature. After catalyst calcination at the highest temperature used in this study, 1200 °C, the palladium particles became much larger due to the loss of the palladium interaction with the support. Only the metal phase of palladium was observed in these catalysts, and their catalytic activity decreases substantially.
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