Optimal parameters for the synthesis of the mesoporous molecular sieve [Si]-MCM-41

被引:155
作者
Cheng, CF [1 ]
Park, DH [1 ]
Klinowski, J [1 ]
机构
[1] UNIV CAMBRIDGE, CHEM LAB, DEPT CHEM, CAMBRIDGE CB2 1EW, ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1997年 / 93卷 / 01期
关键词
D O I
10.1039/a605100f
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
Highly crystalline MCM-41 with a very narrow pore-size distribution (FWHM = 1.5 Angstrom), high surface area (1185 m(2) g(-1)), large grain size and thick channel walls (ca. 17 Angstrom) was prepared in alkali-free media. The properties of the product depend on the source and concentration of the reactants, the gel aging time, the temperature and the duration of the synthesis. There is no induction period in the course of the synthesis and Ostwald's rule of successive transformations applies. The initially produced hexagonal phase is transformed into the lamellar phase and then into an amorphous phase. In the 150 degrees C synthesis the most stable product is amorphous silica. The course of the synthesis is conveniently monitored by pH measurement. Gel aging, during which a spatial distribution of silicate polyanions and micellar cations is established, is essential for preparing high-quality MCM-41. Surfactants with the same cationic organic group but different counter-anions alter the course of the synthesis. The degree of polymerization of silica is also important. Highly basic gels favour the lamellar product; when the gel is weakly basic the quality of MCM-41 is lower as insufficient TMAOH is available to dissolve the silica. The result of excess silica is similar but even more pronounced. Purely lamellar products are made at low SiO2 concentrations, when the gel is more strongly basic. The best quality MCM-41 is prepared from a gel of molar composition SiO2:0.19 TMAOH:0.27 CTABr:40 H2O (with CTABr/SiO2 = 0.27, similar to the ratio in the solid product) aged at 20 degrees C for 24 h and synthesis lasting for 48 h.
引用
收藏
页码:193 / 197
页数:5
相关论文
共 41 条
[11]   Synthesis and characterization of the mesoporous galloaluminosilicate molecular sieve MCM-41 [J].
Cheng, CF ;
Klinowski, J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (02) :289-292
[12]   Synthesis and characterization of the gallosilicate mesoporous molecular sieve MCM-41 [J].
Cheng, CF ;
He, HY ;
Zhou, WZ ;
Klinowski, J ;
Goncalves, JAS ;
Gladden, LF .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (01) :390-396
[13]   THE ROLE OF SURFACTANT MICELLES IN THE SYNTHESIS OF THE MESOPOROUS MOLECULAR-SIEVE MCM-41 [J].
CHENG, CF ;
LUAN, ZH ;
KLINOWSKI, J .
LANGMUIR, 1995, 11 (07) :2815-2819
[14]   CRYSTAL MORPHOLOGY SUPPORTS THE LIQUID-CRYSTAL FORMATION MECHANISM FOR THE MESOPOROUS MOLECULAR-SIEVE MCM-41 [J].
CHENG, CF ;
HE, HY ;
ZHOU, WZ ;
KLINOWSKI, J .
CHEMICAL PHYSICS LETTERS, 1995, 244 (1-2) :117-120
[15]   The unit cell of the gallosilicate mesoporous molecular sieve [Si,Ga]-MCM-41 is significantly smaller than in the purely siliceous [Si]-MCM-41 [J].
Cheng, CF ;
Alba, MD ;
Klinowski, J .
CHEMICAL PHYSICS LETTERS, 1996, 250 (3-4) :328-334
[16]   DIRECT TEM IMAGING OF TUBULES IN CALCINED MCM-41 TYPE MESOPOROUS MATERIALS [J].
CHENITE, A ;
LEPAGE, Y ;
SAYARI, A .
CHEMISTRY OF MATERIALS, 1995, 7 (05) :1015-1019
[17]   SYNTHESIS OF AN ULTRALARGE PORE TITANIUM SILICATE ISOMORPHOUS TO MCM-41 AND ITS APPLICATION AS A CATALYST FOR SELECTIVE OXIDATION OF HYDROCARBONS [J].
CORMA, A ;
NAVARRO, MT ;
PARIENTE, JP .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (02) :147-148
[18]   IMPROVED STABILITY OF MCM-41 THROUGH TEXTURAL CONTROL [J].
COUSTEL, N ;
DIRENZO, F ;
FAJULA, F .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (08) :967-968
[19]  
Engelhardt G., 1987, HIGH RESOLUTION SOLI
[20]  
Gregg S.J., 1982, ADSORPTION SURFACE A, P111