Journal
MICROPOROUS AND MESOPOROUS MATERIALS
Volume 66, Issue 2-3, Pages 143-156Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2003.08.021
Keywords
hydrothermal synthesis; microwave; colloidal silicalite; TS-1; crystal growth; nucleation
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Possible methods for the preparation of colloidal zeolite sols are discussed: direct synthesis is at present the only practicable procedure. The linear crystal growth rate for colloidal TS-1 (approximate to 2.5 at.% Ti) at 175 degreesC was estimated to be,less than or equal to 80 nm h(-1), which is lower than that for colloidal silicalite by at least a factor of 3. The introduction of titanium also caused a reduction in the number of crystals nucleated. These effects are ascribed to the difficulty of incorporating the heteroelement into the lattice. No evidence for Ostwald ripening in colloidal silicalite synthesis was found, even at long reaction times. In seeded growth experiments at 100 degreesC, (i) TPA-silicalite-1 product crystal size could be closely controlled by the quantity of 43 nm seed added, and (ii) crystal linear growth rates in thermally and microwave heated reactions were the same within experimental error. Ageing the precursor sols at 22 degreesC before crystallisation at 90-175 degreesC (microwave or thermal heating) demonstrated the generation of proto-nuclei during the room-temperature ageing process. On subsequent heating, these mature into viable nuclei and grow into crystals. An interpretation of this behaviour establishes the relationship of the present results to those of other workers. This identifies the generation of nuclei with a series of chemical steps which lead from the initial equilibration reactions to the formation of the primary replicating unit. (C) 2003 Elsevier Inc. All rights reserved.
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