Synthesis conditions for hexagonal mesoporous silica layers

被引:98
作者
Klotz, M [1 ]
Ayral, A [1 ]
Guizard, C [1 ]
Cot, L [1 ]
机构
[1] Univ Montpellier 2, ENSCM, Lab Mat & Proc Membranaires, CNRS,UMR 5635, F-34296 Montpellier 5, France
关键词
D O I
10.1039/a906181i
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
Hexagonal mesoporous silica layers were prepared by the sol-gel route using silicon alkoxides as silica precursors and alkyltrimethylammonium bromides to form the templating liquid crystal mesophase. The synthesis conditions required to obtain well-ordered crack-free layers were investigated. Thin layers exhibiting these properties were deposited from diluted sols. X-Ray diffraction enabled characterisation of the thermal evolution of their ordered structure and crystalline texture. Their porosity was experimentally measured from nitrogen adsorption-desorption analyses carried out directly on the thin layers. Two main synthesis parameters were identified. The first is the ageing time of the sol before deposition: Si-29 NMR showed that the disappearance of the ordered structure in the layers is related to the appearance of the Q(3) species in the sol. The second important synthesis parameter is the surfactant volume fraction in the medium after the removal of the volatile components. Using hexadecyltrimethylammonium bromide, well-ordered hexagonal layers were obtained for surfactant volume fractions ranging from 0.5 to 0.65, as expected from the corresponding water-surfactant binary diagram. For surfactants with shorter alkyl chains, the domain of existence of the hexagonal layers shifts to higher surfactant volume fractions in agreement with the evolution previously observed on the water-surfactant binary diagrams.
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页码:663 / 669
页数:7
相关论文
共 39 条
[11]  
DABADIE T, 1994, THESIS U MONTPELLIER
[12]  
Ekwall P, 1975, ADV LIQ CRYST, V1, P1
[13]   PHASE-EQUILIBRIA AND STRUCTURES IN TERNARY-SYSTEMS OF A CATIONIC SURFACTANT (C16TABR OR (C16TA)2SO4), ALCOHOL, AND WATER [J].
FONTELL, K ;
KHAN, A ;
LINDSTROM, B ;
MACIEJEWSKA, D ;
PUANGNGERN, S .
COLLOID AND POLYMER SCIENCE, 1991, 269 (07) :727-742
[14]   INTERMEDIATE LIQUID-CRYSTALLINE PHASES IN THE BINARY-SYSTEM C16TACL-H2O - AN NMR AND LOW-ANGLE X-RAY-DIFFRACTION STUDY [J].
HENRIKSSON, U ;
BLACKMORE, ES ;
TIDDY, GJT ;
SODERMAN, O .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (09) :3894-3902
[15]   Prediction of hysteresis disappearance in the adsorption isotherm of N2 on regular mesoporous silica [J].
Inoue, S ;
Hanzawa, Y ;
Kaneko, K .
LANGMUIR, 1998, 14 (11) :3079-3081
[16]   ORDERED MESOPOROUS MOLECULAR-SIEVES SYNTHESIZED BY A LIQUID-CRYSTAL TEMPLATE MECHANISM [J].
KRESGE, CT ;
LEONOWICZ, ME ;
ROTH, WJ ;
VARTULI, JC ;
BECK, JS .
NATURE, 1992, 359 (6397) :710-712
[17]   Adsorption study of surface and structural properties of MCM-41 materials of different pore sizes [J].
Kruk, M ;
Jaroniec, M ;
Sayari, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (04) :583-589
[18]   Preparation of continuous mesoporous films on porous and dense substrates [J].
Liu, J ;
Bontha, JR ;
Kim, AY ;
Baskaran, S .
MICROPOROUS AND MACROPOROUS MATERIALS, 1996, 431 :245-250
[19]  
Lowell S., 1984, POWDER SURF AREA POR, DOI DOI 10.1007/978-94-009-5562-2_3
[20]   Continuous formation of supported cubic and hexagonal mesoporous films by sol gel dip-coating [J].
Lu, YF ;
Ganguli, R ;
Drewien, CA ;
Anderson, MT ;
Brinker, CJ ;
Gong, WL ;
Guo, YX ;
Soyez, H ;
Dunn, B ;
Huang, MH ;
Zink, JI .
NATURE, 1997, 389 (6649) :364-368