摘要
采用优化的Stber法制备了平均粒径为230 nm的单分散球形SiO2颗粒,并以此为内核,通过水解沉积法制备了不同壳层厚度的核-壳结构SiO2@Fe2O3催化剂。采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、N2物理吸附和X射线衍射分析(XRD)等手段对催化剂进行表征,探讨了不同制备条件对SiO2@Fe2O3催化剂形貌的影响。结果表明,通过水解沉积法制备的SiO2@Fe2O3催化剂具有明显的核-壳结构,并且保持了原始SiO2核的球形形貌,Fe2O3纳米粒子通过-OH的氢键作用连接在SiO2表面,形成了2~10 nm厚的Fe2O3均匀连续包覆层。
The monodisperse SiO2 microspheres with average diameter of 230 nm made by optimized Stber method were used as core to prepare core-shell structure SiO2@ Fe2O3 catalysts with different shell thickness through hydrolysis precipitation. Scanning electron microscopy( SEM), transmission electron microscopy(TEM),N2 physical adsorption and X-ray diffraction( XRD) were used to characterize the size,structure and morphology of catalysts and the effects of different preparation condition on morphology were discussed. The characterization results indicate that SiO2@ Fe2O3 catalysts possess obvious core-shell structure and the spherical morphology of catalyst is kept. Iron oxide nanoparticles are attached to the silica surface through hydroxyl-bond and a 2 ~ 10 nm thick dense shell is formed.
出处
《燃料化学学报》
EI
CAS
CSCD
北大核心
2015年第6期692-700,共9页
Journal of Fuel Chemistry and Technology
基金
国家高技术研究发展计划(863计划
2011AA05A205)