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以金属有机骨架为牺牲模板制备MnOx-CeO2及其催化氧化
引用本文:林雪婷,付名利,贺辉,吴军良,陈礼敏,叶代启,胡芸,王逸凡,WENWilliam.以金属有机骨架为牺牲模板制备MnOx-CeO2及其催化氧化[J].物理化学学报,2018,34(6):719-730.
作者姓名:林雪婷  付名利  贺辉  吴军良  陈礼敏  叶代启  胡芸  王逸凡  WENWilliam
作者单位:1 华南理工大学,环境与能源学院,广州 5100062 广东省大气环境与污染控制重点实验室,广州 5100063 挥发性有机物污染治理技术与装备国家工程实验室,广州 5100064 Centre for Clean Environment and Energy, Environmental Futures Centre, School of Environment, Griffith University, Gold Coast, QLD4222, Australia
基金项目:The project was supported by the National Natural Science Foundation of China(51578245);The project was supported by the National Natural Science Foundation of China(51378213);The project was supported by the National Natural Science Foundation of China(51108187);The project was supported by the National Natural Science Foundation of China(21777047);the Guangdong Natural Science Foundation, China( )
摘    要:以均苯三甲酸合铈-金属有机骨架(CeBTC-MOF)作为模板制备系列不同Mn含量的MnOx-CeO2催化剂,用于甲苯催化氧化。应用X射线衍射(XRD)、N2物理吸附-脱附、热重分析(TG)、元素分析(EA)、电感耦合等离子体发射光谱法(ICP-OES)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、程序升温还原(H2-TPR)、X射线光电子能谱(XPS)、拉曼光谱(Raman)和紫外可见漫反射(UV-vis)等手段对催化剂进行了表征。结果表明,通过MOF模板法制备的复合氧化物具备棒状形貌、高度分散、高比表面积和纳米晶体颗粒等特征。Mn在引入MOF的过程中,一部分进入CeO2晶格形成固溶体,另一部分则分散在CeO2表面,且分散的Mn分为单层分散态和晶相态。其中,CeO2载体表面和Mn分散物之间的强相互作用是影响活性的重要因素。当表面分散的Mn低于单层分散阈值6.2%时,Mn以嵌入模型的形式与表面CeO2发生强相互作用,有效促进催化剂的还原从而提高活性;当表面分散的Mn超过单层分散阈值6.2%时,载体表面形成Mn3O4晶相结构,对活性无明显促进作用。

关 键 词:金属有机骨架  MnOx-CeO2复合氧化物  甲苯  单层分散阈值  氧空位  
收稿时间:2017-10-27

Synthesis of MnOx-CeO2 Using Metal-Organic Framework as Sacrificial Template and Its Performance in the Toluene Catalytic Oxidation Reaction
Xueting LIN,Mingli FU,Hui HE,Junliang WU,Limin CHEN,Daiqi YE,Yun HU,Yifan WANG,William WEN.Synthesis of MnOx-CeO2 Using Metal-Organic Framework as Sacrificial Template and Its Performance in the Toluene Catalytic Oxidation Reaction[J].Acta Physico-Chimica Sinica,2018,34(6):719-730.
Authors:Xueting LIN  Mingli FU  Hui HE  Junliang WU  Limin CHEN  Daiqi YE  Yun HU  Yifan WANG  William WEN
Institution:1. School of Environment and Energy, South China University of Technology, Guangzhou 510006, P. R. China;2. Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control (SCUT), Guangzhou 510006, P. R.China;3. National Engineering Laboratory for VOCs Pollution Control Technology and Equipment, Guangzhou 510006, P. R. China;4. Centre for Clean Environment and Energy, Environmental Futures Centre, School of Environment, Griffith University, Gold Coast, QLD4222, Australia
Abstract:A series of MnOx-CeO2 with different Mn contents was prepared using CeBTC-MOF as the sacrificial template. These constituted a new kind of porous crystalline materials assembled by cerium as metal ions and 1, 3, 5-benzenetricarboxylic acid as organic ligands. The composite oxides exhibited good redox properties and were tested as catalysts in the oxidation of toluene. To obtain insight into the structure-activity relationship of the catalysts, the samples were characterized using powder X-ray diffraction (XRD), nitrogen adsorption-desorption, thermogravimetric analysis (TG), elemental analysis (EA), inductively coupled plasma-optical emission spectrometry (ICP-OES), scanning electron microscopy (SEM), transmission electron microscopy (TEM), H2 temperature-programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy (Raman), and UV-Vis diffuse reflectance spectroscopy. Studies of the CeBTC-MOF template showed that the metal-organic framework could be completely decomposed at a calcination temperature of 300 ℃. Therefore, CeBTC-MOF decomposed and generated CO2 and H2O during the calcination process. The gas molecule spilled out from the structure to form the interior void space. The spilling out could be controlled by varying the calcination temperature. This regulated the quantity and size of the interior void, which in turn made the surface area controllable. The secondary building unit of CeBTC-MOF was oxidized to nano-sized crystalline particles, which exhibited outstanding interfacial contact. SEM and TEM results showed that the composite oxides prepared by pyrolysis of the CeBTC-MOF template exhibited rod-shaped nanocrystalline particles. While introducing Mn into MOF, part of Mn entered the ceria lattice to form solid solution and the remaining Mn was dispersed on CeO2 surface. The elemental mappings revealed a well-proportioned distribution of Mn, which confirmed the successful formation of bimetallic metal oxides using the MOF-template method. All the samples exhibited sizes and shapes similar to their parent MOFs. As for catalytic activity, all the composite oxides showed better performances than pure CeO2 for catalytic oxidation of toluene. This could be attributed to higher concentration of oxygen vacancies, which was characterized by Raman spectroscopy. In addition, the XPS results indicated that Mn4+/(Mn2++Mn3+), Ce4+/Ce3+, Olatt (lattice oxygen), and Osur(surface oxygen) all participated in the redox process during catalytic oxidation of toluene, which helped elucidate the mechanism at a micro level.
Keywords:Metal-Organic Framework  MnOx-CeO2 composite oxides  Toluene  Monolayer dispersion threshold  Oxygen vacanc  
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