Calcination behavior of different surfactant-templated mesostructured silica materials

被引:279
作者
Kleitz, F [1 ]
Schmidt, W [1 ]
Schüth, F [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-54570 Mulheim, Germany
关键词
mesoporous silica; MCM-41; MCM-48; SBA-3; SBA-15; template removal; scattering contrast; high temperature X-ray diffraction;
D O I
10.1016/S1387-1811(03)00506-7
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The removal of the template by calcination from mesostructured M41S and SBA-type silica materials was studied by combining high temperature X-ray diffraction, thermogravimetry-differential thermal analysis and mass spectrometry, allowing detailed in situ investigations during the thermal treatment. A comparison was made between materials with different mesoscopic structures, resulting from different synthesis routes and chemical treatment. The in situ XRD studies showed a strong increase in scattering contrast observed for the low angle reflections occurring when the template is removed from the inside of the pores, irrespective of the type of mesostructure. In agreement with the XRD investigations, the TG-DTA/MS experiments proved that the removal of the surfactant is a stepwise mechanism. Marked differences in the scattering contrast variations and chemical reactions were observed depending on the synthesis conditions and the type of surfactant, which highlight the role of the silica-surfactant interfaces. MCM-41 and MCM-48 materials synthesized in the presence of alkyltrimethylammonium surfactant under alkaline conditions showed a template removal mechanism based on an Hofmann degradation at low temperatures, followed by oxidation and combustion reactions above 250 degreesC. On the other hand, acidic conditions employed for the synthesis of SBA-3 type materials seems to favor reactions of oxidations after the evaporation of water and hydrochloric acid at low temperature. in that case, large contraction of the hexagonal unit cell was usually observed. Most of the block-copolymer template is removed from SBA-15 at lower temperatures, in a single oxidation step. The SBA-15 framework possibly catalyzes the oxidation of the block copolymer template species. In addition, the presence of framework porosity or pore connectivities seems to be responsible for the strong scattering contrast variations observed below 250 degreesC. Residual carbonaceous species and water are removed from the structure upon heating from 300 degreesC up to 550 degreesC. During this subsequent process a large contraction of the hexagonal unit cell is observed, possibly due to further framework condensation. In addition, a brief survey of the previous investigations reported in the literature related to the decomposition of structure-directing agents is given. (C) 2003 Elsevier Inc. All rights reserved.
引用
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页码:1 / 29
页数:29
相关论文
共 89 条
[11]   Postsynthesis hydrothermal restructuring of M41S mesoporous molecular sieves in water [J].
Chen, LY ;
Horiuchi, T ;
Mori, T ;
Maeda, K .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (08) :1216-1222
[12]   Ordered mesoporous materials [J].
Ciesla, U ;
Schüth, F .
MICROPOROUS AND MESOPOROUS MATERIALS, 1999, 27 (2-3) :131-149
[13]   Highly ordered porous zirconias from surfactant-controlled syntheses:: Zirconium oxide-sulfate and zirconium oxo phosphate [J].
Ciesla, U ;
Fröba, M ;
Stucky, G ;
Schüth, F .
CHEMISTRY OF MATERIALS, 1999, 11 (02) :227-234
[14]   A new application of UV-ozone treatment in the preparation of substrate-supported, mesoporous thin films [J].
Clark, T ;
Ruiz, JD ;
Fan, HY ;
Brinker, CJ ;
Swanson, BI ;
Parikh, AN .
CHEMISTRY OF MATERIALS, 2000, 12 (12) :3879-3884
[15]   ACIDITY AND STABILITY OF MCM-41 CRYSTALLINE ALUMINOSILICATES [J].
CORMA, A ;
FORNES, V ;
NAVARRO, MT ;
PEREZPARIENTE, J .
JOURNAL OF CATALYSIS, 1994, 148 (02) :569-574
[16]   From microporous to mesoporous molecular sieve materials and their use in catalysis [J].
Corma, A .
CHEMICAL REVIEWS, 1997, 97 (06) :2373-2419
[17]   THE EFFECT OF THERMAL-TREATMENT AND OF GRINDING ON SILICALITE-1 SYNTHESIZED IN THE PRESENCE OF FLUORIDE IONS [J].
FONSECA, A ;
NAGY, JB ;
ASSWAD, JEA ;
MOSTOWICZ, R ;
CREA, F ;
TESTA, F .
ZEOLITES, 1995, 15 (03) :259-263
[18]   Fe2O3 nanoparticles within mesoporous MCM-48 silica:: In situ formation and characterization [J].
Fröba, M ;
Köhn, R ;
Bouffaud, G ;
Richard, O ;
van Tendeloo, G .
CHEMISTRY OF MATERIALS, 1999, 11 (10) :2858-2865
[19]   Microporosity and connections between pores in SBA-15 mesostructured silicas as a function of the temperature of synthesis [J].
Galarneau, A ;
Cambon, N ;
Di Renzo, F ;
Ryoo, R ;
Choi, M ;
Fajula, F .
NEW JOURNAL OF CHEMISTRY, 2003, 27 (01) :73-79
[20]   The synthesis of micrometer- and submicrometer-size spheres of ordered mesoporous oxide MCM-41 [J].
Grun, M ;
Lauer, I ;
Unger, KK .
ADVANCED MATERIALS, 1997, 9 (03) :254-&