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作 者:郭彬[1] 刘辉[1] 郝志显[1] 甘礼华[1] 徐子颉[1] 陈龙武[1]
机构地区:[1]同济大学化学系,上海200092
出 处:《化学学报》2006年第8期756-760,共5页Acta Chimica Sinica
基 金:同济大学理科基金(No.1380219043)资助项目.
摘 要:利用酸性条件下正硅酸乙酯的水解和脲醛树脂的聚合反应同时一步原位进行的方法合成了二氧化硅复合粉体(包括核壳微球结构和网状结构)和块体凝胶材料.液氮吸附BET分析结果证明复合材料焙烧后得到的二氧化硅孔径分布均匀,大小在介孔范围内.改变反应性单体尿素.甲醛及正硅酸乙酯等的初始浓度可对二氧化硅块体材料的孔径大小进行调节.扫描电子显微镜观测结果显示,随着原料单体初始浓度的变化复合粉体材料的微米级形貌可以是多孔网状结构或核壳结构.从红外光谱和差热分析的结果推测,高甲醛/尿素摩尔比[n(甲醛)∶n(尿素)≥2]条件下形成的支链脲醛树脂可作为块体二氧化硅理想的孔结构导向剂.A simple one-step procedure was described for the synthesis of mesoporous monolith and com- posite sphere, in which hydrolyzation of tetraethyl orthosilicate and polymerization of urea with formaldehyde occurred at the same time. The analysis of the liquid nitrogen adsorption demonstrated that the pore sizes of the monoliths and the composite spheres were both uniform. Morphologies of the composite spheres characterized by SEM were smooth or of network, which depended on the relative concentrations of the reactants. As the molar ratio of formaldehyde to urea exceeded the limit of 2.0, the synthesis by varying initial concentration of the reactants yielded the monoliths with controllable pore sizes. From the analysis of the FTIR and DTA, the urea-formaldehyde resin with branched chains in its molecular structure was considered as an inducing agent in the pore formation of the monolith.
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