Tuning the oxygen storage capacity and oxygen release properties of CeO2-based catalysts for catalytic combustion of toluene

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-09-12 DOI:10.1016/j.mcat.2024.114527
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Abstract

CeO2 with varied doping transition metal was investigated to understand the oxygen storage capacity and oxygen release property of CeO2-based catalysts for toluene combustion. The order of catalytic activity was as follows: CuCeOx ≈ CoCeOx > MnCeOx > FeCeOx > NiCeOx > ZrCeOx > CeO2. Kinetic studies showed that the reaction on CuCeOx proceed via an MvK mechanism and the oxygen of catalyst was crucial factor for the toluene combustion. H2-TPR and XPS showed the addition of transition metal to CeO2 could modify the surface lattice oxygen. Moreover, the oxygen storage capacity and oxygen release properties showed the transition metal additive not only change the amount of oxygen, but also affect the oxygen mobility. A linear relationship was observed between the catalytic activity and oxygen storage capacity. Diffuse reflectance infrared fourier transform spectroscopy showed the toluene first adsorbed on the surface of catalyst, and then reacted with oxygen of catalyst to form benzyl, benzoate and benzyl carbonate species. All these results provided a new strategy to develop high performance catalyst.

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调整用于催化燃烧甲苯的 CeO2 基催化剂的储氧能力和释氧特性
研究了掺杂不同过渡金属的 CeO2,以了解基于 CeO2 的甲苯燃烧催化剂的储氧能力和释氧特性。催化活性顺序如下CuCeOx ≈ CoCeOx > MnCeOx > FeCeOx > NiCeOx > ZrCeOx > CeO2。动力学研究表明,CuCeOx 上的反应是通过 MvK 机制进行的,催化剂中的氧是甲苯燃烧的关键因素。H2-TPR 和 XPS 显示,在 CeO2 中添加过渡金属可以改变表面晶格氧。此外,氧储存能力和氧释放特性表明,过渡金属添加剂不仅改变了氧的量,还影响了氧的流动性。催化活性与储氧能力之间呈线性关系。漫反射红外傅里叶变换光谱显示,甲苯首先吸附在催化剂表面,然后与催化剂中的氧气反应生成苄基、苯甲酸酯和碳酸苄酯。所有这些结果为开发高性能催化剂提供了一种新策略。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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