摘要
采用浸渍法制备了MnO x/CeO2-Al2O3整体催化剂,运用X射线衍射(XRD)和程序升温还原(TPR)方法对催化剂进行了表征,利用恒压排气量气法评价了催化剂分解过氧化氢反应的活性,并用单组元发动机热试考察了整体催化剂分解高浓度过氧化氢反应的稳定性。结果表明,CeO2通过形成表面活性氧和Mn-Ce-O固溶体,强化了MnO x与CeO2-Al2O3载体间的相互作用,将低价态Mn3+氧化到活泼的高价态Mn4+,增加了低温活性中心数,并促进了MnO x的分散,提高了催化剂的还原氧化能力。与MnO x/Al2O3催化剂相比,MnO x/CeO2-Al2O3整体催化剂对高浓度过氧化氢分解反应具有较高的活性和稳定性。
M nO x/ C eO2-Al2O3monolith catalysts w ere prepared by impregnation method. T he catalysts w ere characterized by X-ray diffraction( XR D) and temperature-programmed reduction( T PR) methods,T he H2O2decomposition reaction activity w as determined by oxygen-gasometry of the reaction kinetics in a constant pressure reactor. T he stability of monolith catalysts for the decomposition of high concentration hydrogen peroxide w as evaluated in a monopropellant thrust hot test system using 90% H2O2. T he results show that C eO2can promote the interaction betw een M nO x and C eO2,the dispersion of Mn species,and the oxidation of low value Mn3 +to more active high value M n4 +,through the formation of surface active oxygen and Mn-Ce-O solid solution. The rise of more active Mn species of Mn4 +increases the number of low temperature active sites and the ability of reduction-oxidation of catalysts. M nO x/ C eO2-Al2O3monolith catalyst has a higher activity and stability for high concentration hydrogen peroxide decomposition reaction,compared to M nO x/ Al2O3monolith catalyst.
出处
《含能材料》
EI
CAS
CSCD
北大核心
2014年第2期148-154,共7页
Chinese Journal of Energetic Materials
基金
国家自然科学基金资助(21076211
21376236)
关键词
物理化学
高浓度过氧化氢
催化分解
整体催化剂
氧化铈
锰氧化物
physical chemistry
high concentration hydrogen peroxide
catalytic decomposition
monolith catalyst
ceria
manga-nese oxide