Ohkubo Takahiro, Ogura Taku, Sakai Hideki, Abe Masahiko
Institute of Colloid and Interface Science, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
J Colloid Interface Sci. 2007 Aug 1;312(1):42-6. doi: 10.1016/j.jcis.2007.02.043. Epub 2007 Feb 21.
We applied a molecular assembly formed in an aqueous surfactant mixture of cationic cetyltrimethylammonium bromide (CTAB) and anionic sodium octylsulfate (SOS) as templates of mesoporous silica materials. The hexagonal pore size can be controlled between 3.22 and 3.66 nm with the mixed surfactant system. In addition, we could observe the lamellar structure of the mixed surfactants with precursor molecules, which strongly shows the possibility of precise control of both the pore size and the structure of pores by changing the mixing ratio of surfactants. Moreover, use of the cationic surfactant having longer hydrophobic chain like stearyltrimethylammonium bromide (STAB) caused the increase in d(100) space and shifted the point of phase transition from hexagonal phase to lamellar phase to lower concentration of SOS.
我们将在阳离子十六烷基三甲基溴化铵(CTAB)和阴离子辛基硫酸钠(SOS)的水性表面活性剂混合物中形成的分子聚集体用作介孔二氧化硅材料的模板。通过混合表面活性剂体系,六边形孔径可控制在3.22至3.66纳米之间。此外,我们可以观察到混合表面活性剂与前驱体分子的层状结构,这有力地表明了通过改变表面活性剂的混合比例来精确控制孔径和孔结构的可能性。此外,使用具有更长疏水链的阳离子表面活性剂,如硬脂基三甲基溴化铵(STAB),会导致d(100)间距增加,并使相变点从六方相转变为层状相的SOS浓度降低。