Solid-state preparation of mesoporous Ce-Mn-Co ternary mixed oxide nanoparticles for catalytic degradation of methylene blue
固态 mesoporous CeMnCo 的准备为甲又蓝色的催化降级的第三的混合氧化物 nanoparticles作者机构:Key Laboratory of Chemical Utilization of Plant Resources of NanchangCollege of ScienceJiangxi Agricultural UniversityNanchang 330045China
出 版 物:《Journal of Rare Earths》 (稀土学报(英文版))
年 卷 期:2021年第39卷第7期
页 面:826-834,I0003页
核心收录:
学科分类:083002[工学-环境工程] 0830[工学-环境科学与工程(可授工学、理学、农学学位)] 081705[工学-工业催化] 07[理学] 070205[理学-凝聚态物理] 08[工学] 0817[工学-化学工程与技术] 080501[工学-材料物理与化学] 080502[工学-材料学] 0805[工学-材料科学与工程(可授工学、理学学位)] 0702[理学-物理学]
基 金:Project supported by the National Natural Science Foundation of China(21403093,21563014) the Foundation of Jiangxi Educational Committee(GJJ170278,GJJ190241) Jiangxi Province Key Research and Development Project(20192BBEL50029)
主 题:Ce-Mn-Co mixed Oxide Methylene blue Advanced oxidation processes Soft reactive grinding Rare earths
摘 要:Mesoporous Ce-Mn-Co ternary metal oxide was fabricated via an efficient oxalate-precursor-based soft reactive grinding route and used to activate H_(2)O_(2) for advanced oxidation of methylene blue in *** addition,Mn-Co binary oxide and pure Co_(3)O_(4) and Mn_(3)O_(4) were also synthesized as reference *** catalysts were characterized by X-ray diffraction,N_(2) adsorption-desorption,H_(2)-temperature programmed reduction,transmission electron microscopy,scanning electron microscopy and X-ray photoelectron *** results demonstrate that part of the Ce and Mn can be incorporated into the lattice of Co_(3)O_(4) and cause severe lattice distortion of the unit *** with the single or binary system,Ce-Mn-Co ternary metal oxide exhibits the best activity in methylene blue removal and nearly 100% decomposition rate and 84% COD removal rate can be achieved in 12 h,and with degradation rate of 93.5% after three *** results are primarily attributed to the synergistic effect of Ce,Mn and Co,which can promote the formation of more lattice defects,higher specific surface area and smaller particle *** tests show that hydroxyl radicals(·OH) play more dominant role than superoxide radicals(·O_(2)^(-)).Kinetic studies were studied and the activation energies of all the catalysts were calculated.