Characterization of the porous structure of SBA-15

被引:1312
作者
Kruk, M
Jaroniec, M [1 ]
Ko, CH
Ryoo, R
机构
[1] Kent State Univ, Dept Chem, Kent, OH 44242 USA
[2] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Taejon 305701, South Korea
关键词
D O I
10.1021/cm000164e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
SBA-15 ordered mesoporous silicas were synthesized using the method reported by Zhao et al, The structures of these materials were characterized using powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), and nitrogen adsorption. The samples were found to exhibit structural properties similar to those reported earlier. Our study confirmed that the size of primary mesopores of SBA-15 can be tailored by the choice of synthesis temperature and that SBA-15 exhibits a significant amount of disordered micropores and small mesopores, The volume and size of these complementary pores were found to be dependent to some extent on the synthesis/aging temperature. It was shown that the washing of as-synthesized SBA-15 in water or ethanol was accompanied by an appreciable structural shrinkage and led to the removal of a significant part of the polymeric template. Therefore, washing needs to be avoided if one wants to isolate SBA-15 without appreciable loss of the template. It was confirmed that water-washed SBA-15 samples have fully accessible primary mesopores. Ethanol-washed samples also were found to exhibit accessible porosity. Despite an appreciable content of the template in the water- and ethanol-washed samples, their pore sizes were usually larger than those of the calcined materials. The observed structural properties of SBA-15 and their dependence on the synthesis temperature and washing were attributed to the changes in the degree of penetration of the poly(ethylene oxide) chains of the triblock copolymer template within the siliceous walls of SBA-15.
引用
收藏
页码:1961 / 1968
页数:8
相关论文
共 72 条
[1]   Kinetics of cosurfactant-surfactant-silicate phase behavior.: 1.: Short-chain alcohols [J].
Ågren, P ;
Lindén, M ;
Rosenholm, JB ;
Schwarzenbacher, R ;
Kriechbaum, M ;
Amenitsch, H ;
Laggner, P ;
Blanchard, J ;
Schüth, F .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (29) :5943-5948
[2]   POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) BLOCK-COPOLYMER SURFACTANTS IN AQUEOUS-SOLUTIONS AND AT INTERFACES - THERMODYNAMICS, STRUCTURE, DYNAMICS, AND MODELING [J].
ALEXANDRIDIS, P ;
HATTON, TA .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1995, 96 (1-2) :1-46
[3]   SELF-AGGREGATION AND PHASE-BEHAVIOR OF POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) POLY(ETHYLENE OXIDE) BLOCK-COPOLYMERS IN AQUEOUS-SOLUTION [J].
ALMGREN, M ;
BROWN, W ;
HVIDT, S .
COLLOID AND POLYMER SCIENCE, 1995, 273 (01) :2-15
[4]  
Antonietti M, 1998, ADV MATER, V10, P154, DOI 10.1002/(SICI)1521-4095(199801)10:2<154::AID-ADMA154>3.0.CO
[5]  
2-I
[6]   LIQUID-CRYSTALLINE PHASES AS TEMPLATES FOR THE SYNTHESIS OF MESOPOROUS SILICA [J].
ATTARD, GS ;
GLYDE, JC ;
GOLTNER, CG .
NATURE, 1995, 378 (6555) :366-368
[7]  
Bae SJ, 2000, CHEM COMMUN, P31
[8]   Mesoporous [M]-MSU-x metallo-silicate catalysts by non-ionic polyethylene oxide surfactant templating acid [N0(N+)X-I+] and base (N0M+I-) catalysed pathways [J].
Bagshaw, SA ;
Kemmitt, T ;
Milestone, NB .
MICROPOROUS AND MESOPOROUS MATERIALS, 1998, 22 (1-3) :419-433
[9]   Bimodal pore systems in non-ionically templated [Si]-MSU-X mesoporous silica through biomimetic synthesis in weakly ionic solutions [J].
Bagshaw, SA .
CHEMICAL COMMUNICATIONS, 1999, (18) :1785-1786
[10]   Modification of [M]-MSU-X mesoporous silicate pore morphology by post-synthesis treatment [J].
Bagshaw, SA .
CHEMICAL COMMUNICATIONS, 1999, (03) :271-272