School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, PR China.
J Colloid Interface Sci. 2011 Jan 15;353(2):519-23. doi: 10.1016/j.jcis.2010.09.086. Epub 2010 Oct 20.
Ti-MCM-41 and Ti-MCM-48 are successfully prepared by one step synthesis and post-synthesis at room temperature. The samples have been characterized by X-ray diffraction, SEM, TEM, nitrogen adsorption/desorption isotherms and UV-Vis spectroscopy. The results demonstrate the existence of an ordered mesoporous structure. The Ti species are grafted into the pure silica sieve frameworks without any evidence of the formation of non-skeleton anatase. The post-synthesis Ti-MCM-41 regular nano-particles display a higher conversion and selectivity as compared to that for both the post-synthesis Ti-MCM-48 and Ti-MCM-41 with ordinary particles, in the epoxidation of cis-cyclooctene with aqueous H(2)O(2) as an oxidant. The enhanced catalytic activity may be attributed to the existence of a higher number of isolated tetracoordinated Ti active sites and regular nano-particles, which are conducive to the affinity of the reactants with active sites.
Ti-MCM-41 和 Ti-MCM-48 采用一步合成和室温后合成法成功制备。采用 X 射线衍射、SEM、TEM、氮气吸附/脱附等温线和 UV-Vis 光谱对样品进行了表征。结果表明存在有序介孔结构。Ti 物种接枝到纯硅筛骨架中,没有任何非骨架锐钛矿形成的证据。与普通颗粒的后合成 Ti-MCM-48 和 Ti-MCM-41 相比,后合成 Ti-MCM-41 规则纳米颗粒在 cis-环辛烯与水相 H2O2 作为氧化剂的环氧化反应中表现出更高的转化率和选择性。增强的催化活性可能归因于存在更高数量的孤立四配位 Ti 活性位和规则纳米颗粒,这有利于反应物与活性位的亲和力。