摘要
采用热分解法、溶胶-凝胶法、沉淀法和水热法制备了CeO_2载体,SEM、XRD表征、N_2低温吸脱附和氢气程序升温还原(H2-TPR)实验和结果分析显示,溶胶-凝胶法制备样品具有更优的比表面积、孔容、孔径和氧化还原性能,故选择溶胶-凝胶法制备Ti_(0.5)Ce_(0.5)O_2混合氧化物催化载体。使用XRD、SEM、N2低温吸脱附、H2-TPR等分析手段对产物的物相特征、吸附性能和氧化还原性能进行了表征。Ti_(0.5)Ce_(0.5)O_2的H2-TPR在261、529和749℃处出现耗氢峰,分别归属于表面吸附氧的还原、表面晶格氧的还原和体相晶格氧的还原,TEM结果表明Ti4+离子进入CeO_2晶格形成TiO_2-CeO_2填隙固溶体,固溶体的形成有利于载体氧化还原能力的增强。
The CeO2 carriers were prepared by thermal decomposition,sol-gel,precipitation and hydrothermal methods.The results of XRD and SEM analysis,N2 adsorption-desorption isotherms and H2-temperature-programmed reduction(H2-TPR)patterns showed that the CeO2 particles obtained by sol-gel method possess good specific surface area,pore volume,pore diameter,and redox performance.Therefore,The mixed oxide catalyst carrier Ce0.5Ti0.5O2 was prepared by sol-gel method.The phase analysis,adsorption and redox properties of samples were investigated.The positions of hydrogen consumption peak of Ce0.5Ti0.5O2H2-TPR pattern were 261,529 and 749 ℃,attributed to adsorbed oxygen redox on the surface,lattice oxygen redox on the surface and the body phase lattice oxygen redox,respectively.The result of TEM showed that Ti^4+ entered into the CeO2 lattice and formed interstitial solid solution,it not only reduced the reduction temperature of CeO2 and TiO2,but also enhanced the redox property.
作者
刘欣
贾伟
张爱琴
申倩倩
贾虎生
许并社
LIU Xin;JIA Wei;ZHANG Aiqin;SHEN Qianqian;JIA Husheng;XU Bingshe(Key Laboratory of Interface Science and Engineering in Advanced Materials of Ministry of Education,Taiyuan University of Technology,Taiyuan 030024,China;College of Materials Science and Engineering,Taiyuan University of Technology,Taiyuan 030024,China;China National Offshore Oil Taiyuan Precious Metals Co.,Ltd.,Taiyuan 030006,China;Research Centre of Advanced Materials Science and Technology,Taiyuan University of Technology,Taiyuan 030024,China)
出处
《中国材料进展》
CAS
CSCD
北大核心
2019年第4期401-409,共9页
Materials China
基金
国家自然科学基金项目(51402209)
山西省基础研究项目(2015021075
201601D102020
201701D221083)
山西省科技攻关计划项目(20140321012-01
201603D121017)
山西省高校科技创新研究项目(2016124)
太原理工大学校基金项目(2015MS046
2016QN86
2017QN83)