ABSTRACT
Well crystallized silicalite-1 has been obtained from three sources of amorphous silica, namely, rice hull ashes, commercial Davisil, and a fume silica from Aldrich. The silicas were first dissolved in glycerol according to a recently described reaction. This reaction transforms rapidly and efficiently large surface area silicates into poly-alkoxide gels. It can be schematized as an etherification of an alcohol function of glycerol by the weakly acid surface silanol groups. The facile hydrolysis of the alkoxide permits the preparation of relatively pure and reactive silica, keeping the mesoporous character of the parent starting material. We insist on the mesoporous character of the solids obtained upon hydrolyzing the organo-silicic gel because we believe the gel plays a role of template in the secondary synthesis of mesoporous structures. The hydrolysis is carried out in presence of a structure directing agent, namely tetra-propylammonium hydroxide, TPAOH. After aging, the residue is dried and calcined. The first advantage of using the organo-silicic gel is probably related to the high degree of depolymerization of silica, witness by the C/Si ratio. The second one, more subtle to define, is to provide an intermediate silica with hydrophilic a hydrophobic regions, interfering differently with the surfactant. After calcination at 500 degrees C, well crystallized silicalite-1 is obtained. The texture of the starting silica influences the textural characteristics of the final silicalite-1.
ABSTRACT
As shown recently, the networks of mesoporous high-surface-area silicates and zeolites undergo a deep depolymerization process in glycerol, near 200 degrees C. Within 1 h, X-ray diffraction analysis amorphous gels are obtained. However, some local ordering subsists as demonstrated by a striking similarity between the silicon and aluminum high-resolution solid-state NMR spectra before and after the reaction. The residual organization could be investigated indirectly in studying the recrystallization of these gels in the presence or absence of structure-directing agents. Were this attempt successful, the way should be opened for the synthesis of molecular sieves starting from gels obtained from naturally occurring zeolites. Here, it will be shown that an amorphous gel obtained from HZSM-5 recovers the initial long-range structure of the parent material in a few hours at 85 degrees C in the presence of an aqueous solution of tetrapropyl ammonium (TPA) or NH3. The recrystallization of HY requires the presence of tetramethylammonium, but about 25% of the crystallization is obtained rapidly (approximately = 1 day) at 80 degrees C with ammonia. Hypotheses about the preorganized structural units are presented. The value of the Si-O-Si angle in the silica cluster seems to be of paramount importance.
ABSTRACT
In glycerol, near 200 degrees C, the silicate networks of mesoporous silicates and zeolites undergo a deep depolymerization process. In a few hours, depending on the initial concentration of the solid in glycerol and on the temperature, amorphous gels are obtained. In these gels, a fraction of the Si-O-Si bonds are transformed into Si-O-C. The constitutional aluminum remains bound to the silica network in the gel. The short range ordering is maintained to some extent: the size of the smallest structural unit in gels obtained from zeolites is in the range of the cubic nanometer, nm3.
