化学学报 ›› 2011, Vol. 69 ›› Issue (02): 226-230. 上一篇    下一篇

研究论文

有序介孔碳的合成及其相转变机理的研究

李猛,俞建长*   

  1. (福州大学材料科学与工程学院 福州 350108)
  • 投稿日期:2010-07-04 修回日期:2010-08-20 发布日期:2010-09-26
  • 通讯作者: 李猛 E-mail:limeng42525@163.com
  • 基金资助:

    福建省自然科学基金

Synthesis and Phase Transition of Ordered Mesoporous Carbon

LI Meng, YU Jian-Chang   

  1. (College of Materials Science and Engineering, Fuzhou University, Fuzhou 350108)
  • Received:2010-07-04 Revised:2010-08-20 Published:2010-09-26

采用十六烷基三甲基溴化铵(CTAB)作为模板剂, 正硅酸乙酯(TEOS)为硅源, 在碱性条件下, 用低温合成方法合成了有序介孔硅, 并以此为硬模板, 蔗糖为碳前驱体, 采用液相浸渍方法填充碳源, 制备出有序介孔碳. 通过XRD、TEM、N2吸附-脱附等测试方法对其表征, 结果表明合成的介孔材料高度有序, 均具有很高的比表面积(介孔硅, 992~1096 m2/g; 介孔碳, 930~1208 m2/g), 较大的孔容和较窄的孔径分布. 还发现随着反应温度的升高, 介孔硅的结构从二维六方相(p6mm)转变为三维立方相(Ia3d); 介孔碳在复制介孔硅后, 其结构也从三维立方相(Ia3d)转变为四方相(I41/a), 并对相转变机理做了初步探讨.

关键词: 介孔硅, 介孔碳, 相转变

Mesoporous silica materials have been synthesized at low temperature under alkaline condition using tetraethyl orthosilicate as the silica source and cetyltrimethylammonium bromide as the structure directing agent. And the ordered mesoporous carbon was synthesized by liquid impregnation method with sucrose as the carbon precursor and mesoporous silica as template. The resulting materials were characterized by X-ray di?raction, transmission electron microscopy and N2 adsorption-desorption. The results show that the mesoporous materials have highly ordered structure, high specific surface area (mesoporous silica, 992~1096 m2/g; mesoporous carbon, 930~1208 m2/g), large pore volume and narrow pore size distribution. In addition, with the rising of reaction temperature, the phase transformation of mesoporous silica from hexagonal p6mm to cubic Ia3d was observed, and the structure of mesoporous carbon replicated from silica template transformed from cubic Ia3d to tetragonal I41/a. The preliminary discussion on phase transition was carried on.

Key words: mesoporous silica, mesoporous carbon, phase transition

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