Influence of Pd and Rare Earth Metals Oxides (Ce, La) as Modifying Additives in the Co,Ni-Oxide Catalyst Compositions on the Process of Methane Oxidation

IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
S. O. Soloviev, G. R. Kosmambetova, P. I. Kyriienko, D. E. Samoilenko, Y. P. Kurylets
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引用次数: 0

Abstract

NiO-Al2O3 and Co3O4 oxide catalysts modified with palladium and oxides of rare earth metals (Ce and La) and formed on structured cordierite supports have been studied in the process of methane oxidation at different O2/CH4 ratios. It is shown that methane oxidation proceeds without the formation of CO even at an O2/CH4 ratio of < 2 (in contrast to nickel-containing catalysts) in the presence of cobalt-containing catalysts modified with cerium and lanthanum oxides. The addition of CeO2 promotes Co3O4 dispersion, increases the number of oxygen vacancies, and prevents agglomeration of the active phase of the catalyst at high temperatures. The modification of Co3O4-CeO2/cordierite with palladium (0.1%) enhances its activity due to increased surface oxygen mobility as a result of the interphase interaction of palladium with cobalt oxides and ceria (according to the TPR-H2 and XPS data).

Abstract Image

Pd和稀土金属氧化物(Ce, La)作为Co, ni -氧化物催化剂组合物中改性剂对甲烷氧化过程的影响
研究了在不同O2/CH4比下甲烷氧化过程中,以钯和稀土金属氧化物(Ce和La)改性并在结构堇青石载体上形成的NiO-Al2O3和Co3O4氧化物催化剂。结果表明,当O2/CH4的比值为<时,甲烷氧化过程不生成CO;2(与含镍催化剂相反)在用铈和镧氧化物修饰的含钴催化剂存在下。CeO2的加入促进了Co3O4的分散,增加了氧空位的数量,防止了催化剂活性相在高温下的团聚。用0.1%的钯修饰Co3O4-CeO2/堇青石,由于钯与钴氧化物和铈的相间相互作用,增加了表面氧的迁移率,从而提高了其活性(根据TPR-H2和XPS数据)。
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来源期刊
Theoretical and Experimental Chemistry
Theoretical and Experimental Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
1.60
自引率
10.00%
发文量
30
审稿时长
6-12 weeks
期刊介绍: Theoretical and Experimental Chemistry is a journal for the rapid publication of research communications and reviews on modern problems of physical chemistry such as: a) physicochemical bases, principles, and methods for creation of novel processes, compounds, and materials; b) physicochemical principles of chemical process control, influence of external physical forces on chemical reactions; c) physical nanochemistry, nanostructures and nanomaterials, functional nanomaterials, size-dependent properties of materials.
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