O. A. Bulavchenko, T. N. Afonasenko, V. P. Konovalova, V. A. Rogov, E. Yu. Gerasimov, E. E. Aidakov, Z. S. Vinokurov
{"title":"Effect of the Calcination Temperature on the Properties of MnOx–CuO–ZrO2–CeO2 Catalysts for CO Oxidation","authors":"O. A. Bulavchenko, T. N. Afonasenko, V. P. Konovalova, V. A. Rogov, E. Yu. Gerasimov, E. E. Aidakov, Z. S. Vinokurov","doi":"10.1134/S0022476624070084","DOIUrl":null,"url":null,"abstract":"<p>Four-component oxide catalysts MnO<sub><i>x</i></sub>–CuO–ZrO<sub>2</sub>–CeO<sub>2</sub> are synthesized by co-precipitation with varying the calcination temperature from 400 °C to 800 °C. Formation and decomposition processes in mixed oxides are studied by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. The <i>redox</i> properties of the obtained samples are tested by temperature-programmed hydrogen reduction, and the catalytic characteristics are examined in the CO oxidation reaction. At 400-600 °C homogeneous solid solution Mn<sub><i>x</i></sub>Cu<sub><i>y</i></sub>Zr<sub><i>z</i></sub>Ce<sub><i>q</i></sub>O<sub>2</sub> with the fluorite structure is formed. Temperature elevation to 700-800 °C facilitates the gradual decomposition of initial oxide, with manganese and copper cations leaving its composition in the form of highly dispersed CuO and Cu<sub><i>x</i></sub>Mn<sub>3–<i>x</i></sub>O<sub>4</sub> particles. The occurrence of different active states in the catalyst and their transitions into each other under the temperature effect is shown to maintain the high activity in the CO oxidation reaction up to 800 °C.</p>","PeriodicalId":668,"journal":{"name":"Journal of Structural Chemistry","volume":"65 7","pages":"1371 - 1386"},"PeriodicalIF":1.2000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Structural Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S0022476624070084","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Four-component oxide catalysts MnOx–CuO–ZrO2–CeO2 are synthesized by co-precipitation with varying the calcination temperature from 400 °C to 800 °C. Formation and decomposition processes in mixed oxides are studied by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. The redox properties of the obtained samples are tested by temperature-programmed hydrogen reduction, and the catalytic characteristics are examined in the CO oxidation reaction. At 400-600 °C homogeneous solid solution MnxCuyZrzCeqO2 with the fluorite structure is formed. Temperature elevation to 700-800 °C facilitates the gradual decomposition of initial oxide, with manganese and copper cations leaving its composition in the form of highly dispersed CuO and CuxMn3–xO4 particles. The occurrence of different active states in the catalyst and their transitions into each other under the temperature effect is shown to maintain the high activity in the CO oxidation reaction up to 800 °C.
摘要 通过共沉淀法合成了 MnOx-CuO-ZrO2-CeO2 四组分氧化物催化剂。通过 X 射线衍射、透射电子显微镜和 X 射线光电子能谱研究了混合氧化物的形成和分解过程。通过温度编程氢还原测试了所得样品的氧化还原特性,并考察了 CO 氧化反应的催化特性。在 400-600 °C 温度下,形成了具有萤石结构的均匀固溶体 MnxCuyZrzCeqO2。温度升高到 700-800 ℃时,初始氧化物逐渐分解,锰和铜阳离子以高度分散的 CuO 和 CuxMn3-xO4 颗粒的形式离开其成分。催化剂中不同活性态的出现以及它们在温度作用下的相互转化表明,催化剂在 CO 氧化反应中的高活性可以维持到 800 ℃。
期刊介绍:
Journal is an interdisciplinary publication covering all aspects of structural chemistry, including the theory of molecular structure and chemical bond; the use of physical methods to study the electronic and spatial structure of chemical species; structural features of liquids, solutions, surfaces, supramolecular systems, nano- and solid materials; and the crystal structure of solids.