催化作用
钇
材料科学
X射线光电子能谱
无机化学
电子顺磁共振
八面体
拉曼光谱
穆斯堡尔谱学
化学
晶体结构
结晶学
化学工程
氧化物
核磁共振
冶金
有机化学
物理
光学
工程类
作者
José Vitor C. do Carmo,Rita de Cássia F. Bezerra,Y. Guerra,R. Peña‐Garcia,Alcinéia C. Oliveira,E. Padrón‐Hernández,Gilberto D. Saraiva,J.M. Soares,A.J. Ramiro de Castro,Samuel Tehuacanero-Cuapa,Elena Rodríguez‐Aguado,Enrique Rodríguez‐Castellón
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2022-09-11
卷期号:12 (9): 1033-1033
被引量:5
标识
DOI:10.3390/catal12091033
摘要
A series of the Cr-containing erbium substituted yttrium iron garnet ferrites (ECYIG) was synthesized with distinct Cr amounts, herein referred to as Y3(Er0.02Fe5Cr1−x)O12, where x refers to Cr amounts from 0 to 0.05. The catalytic performance of the solids was investigated in ethylbenzene oxidation in the presence of hydrogen peroxide to assess the role of Cr and Er present in the YIG garnet lattice for fine chemistry compound production. Raman spectroscopy, HRTEM, EPR and FTIR revealed that the insertion of Er (at a fixed amount of 2%) in dodecahedral sites had a great impact on the catalytic activity of the garnets. Both Er3+ and Y3+ in the lattice simultaneously provided structural stability to the garnet structure in any harsh environment. XPS and EPR indicated that the Cr3+ ions replaced those of Fe3+ located in both octahedral and tetrahedral sites of the YIG garnets. The Cr3+ ions acted as electronic promoter to increase the oxidation rate of the Fe3+ active species responsible for activating the EB molecule. SEM-EDS demonstrated that the solids having Cr amounts lower than 4% experienced the most severe deactivation due to the Cr leaching and strong carbon species adsorption on the surface of the catalysts, which decreased their efficiency in the reaction.
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