Facile synthesis and morphology control of highly ordered cubic mesoporous silica SBA-1 using short chain dodecyltrimethylammonium chloride as the structure-directing agent

被引:11
|
作者
Ting, Chun-Chiang [1 ]
Wu, Hao-Yiang [2 ]
Palani, Arudra [1 ]
Chiang, Anthony S. T. [3 ]
Kao, Hsien-Ming [1 ]
机构
[1] Natl Cent Univ, Dept Chem, Chungli 32054, Taiwan
[2] Triserv Gen Hosp, Natl Def Med Ctr, Dept Neurol Surg, Taipei 11490, Taiwan
[3] Natl Cent Univ, Dept Chem & Mat Engn, Chungli 32054, Taiwan
关键词
Mesoporous silica SBA-1; Dodecyltrimethylammonium chloride; Template;
D O I
10.1016/j.micromeso.2008.04.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We presented a facile synthesis route for the formation of highly ordered cubic mesoporous silicas SBA-1 (Pm3n mesophase) with rich morphologies over a broad synthesis temperature range and synthesis compositions by using dodecyltrimethylammonium chloride (C(12)TMACl), a surfactant with a relatively short alkyl chain as compared to the conventional C(16)TMABr often used for the synthesis of the M41S materials, as the template under strongly acidic conditions. Various synthesis parameters such as HCI concentration, synthesis temperature, and surfactant concentrations were systematically investigated. The materials thus obtained were characterized by a variety of techniques including powder X-ray diffraction (XRD), solid-state Si-29 nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscopy (SEM), and nitrogen sorption measurements. It was found that increasing the synthesis temperature and HCI concentration during the synthesis not only enhanced the cross-linking degree of silica framework, as revealed by Si-29 magic angle spinning (MAS) NMR, but also prevented the undesirable phase transformation that was often observed in the conventional synthesis of pure silica SBA-1. By controlling the synthesis temperature and compositions, rich morphologies (cubic, octadecahedron, spherical, edged-truncated cube) of the SBA-1 particles can be obtained. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 329
页数:7
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