State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, Hubei, China.
J Colloid Interface Sci. 2011 Aug 1;360(1):86-92. doi: 10.1016/j.jcis.2011.03.084. Epub 2011 Apr 12.
A layer of macrocyclic calix[4]arene derivatives has been grafted on the internal surface of the mesochannels of the ordered mesoporous SBA-15 to develop highly efficient trap for heavy transition metal (HTM) ions. To ensure the successful anchoring of calix[4]arene derivatives on the surface of SBA-15, two different types of calix[4]arene derivatives, one with one trimethoxysilane functional group and another with two trimethoxysilane functional groups have been explored. XRD, N(2) adsorption and TEM results provide strong evidence that the mesoporous structure of the supporting materials retain their long range ordering throughout the grafting process. Solid-state NMR, TG and FT-IR spectroscopy indicate that both types of calix[4]arene derivatives can be well-anchored on the surface of the wall of SBA-15. Calix[4]arene derivative with only one trimethoxysilane functional group showed high grafting efficiency compared to that with two trimethoxysilane functional groups due to the intramolecular and intermolecular polycondensation between two trimethoxysilane functional groups. The HTM ions extraction capacity in aqueous solution of macrocycle functionalized SBA-15 nanohybrides for a series of HTM ions has been studied. The obtained materials demonstrated very high HTM ions extraction capacity up to 96% for Pb(2+) in aqueous solution.
已经在有序介孔 SBA-15 的介孔内部表面上接枝了一层大环杯[4]芳烃衍生物,以开发用于高效捕获重金属(HTM)离子的陷阱。为了确保杯[4]芳烃衍生物成功接枝到 SBA-15 表面上,探索了两种不同类型的杯[4]芳烃衍生物,一种带有一个三甲氧基硅烷官能团,另一种带有两个三甲氧基硅烷官能团。XRD、N2 吸附和 TEM 结果提供了有力的证据,表明支撑材料的介孔结构在接枝过程中保持其长程有序。固态 NMR、TG 和 FT-IR 光谱表明,两种类型的杯[4]芳烃衍生物都可以很好地接枝到 SBA-15 壁的表面上。与带有两个三甲氧基硅烷官能团的杯[4]芳烃衍生物相比,带有一个三甲氧基硅烷官能团的杯[4]芳烃衍生物的接枝效率更高,这是由于两个三甲氧基硅烷官能团之间的分子内和分子间缩聚。已经研究了一系列 HTM 离子在水溶液中大环官能化 SBA-15 纳米杂化物对 HTM 离子的萃取能力。所得到的材料表现出非常高的 HTM 离子萃取能力,在水溶液中对 Pb(2+)的萃取能力高达 96%。