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Studies on the Role of Fluoride Ion vs Reaction Concentration in Zeolite Synthesis

Zones, Stacey I.; Darton, Richard J.; Morris, Russell; Hwang, Son-Jong

Authors

Stacey I. Zones

Russell Morris

Son-Jong Hwang



Abstract

This work is an experimental response to an intriguing paper recently published by Catlow and co-workers, which looked at the computational feasibility of fluorine location in three different all-silica zeotypes (Attfield, M. P.; Catlow, C. R. A.; Sokol, A. A. Chem. Mater. 2001, 13, 4708). The materials were chosen as representative of three unique host locations. Our present work examined the synthesis of zeotypes AST, IFR, and MTT using organo-cations with a strong preference for crystallizing these structures. We studied the effect of reaction time and the H2O/SiO2 reactant ratio. The latter is probably the most important function in these zeolite crystallizations that use HF. As reaction conditions became more dilute, AST gave way to SGT and IFR to MTW as host structures, while the MTT synthesis was invariant. Our reactions were studied in terms of product yield vs time, product organo-cation content, fluorine content, and the representative 29Si and 19F NMR spectra for certain samples. A single crystal study was carried out for a sample of MTT. Our results showed that, consistent with other recent studies, low H2O/SiO2 reactant ratios lead to more open framework host structures (i.e., IFR vs MTW), and there is typically a higher uptake of organo-cation and fluorine. The structure may well contain a higher population of 4-rings within the silicate substructure. While MTT that contains no 4-rings was chosen as the best possible candidate to achieve an ion-pair for the organo-cation and fluoride anion within the silicate host, both NMR and single crystal work confirm that fluoride is bonded to a 5-coordinate silica center within the lattice.

Citation

Zones, S. I., Darton, R. J., Morris, R., & Hwang, S. (2005). Studies on the Role of Fluoride Ion vs Reaction Concentration in Zeolite Synthesis. Journal of Physical Chemistry B, 109(1), 652-661. https://doi.org/10.1021/jp0402434

Journal Article Type Article
Online Publication Date Dec 7, 2004
Publication Date Jan 1, 2005
Deposit Date Jun 14, 2023
Journal The Journal of Physical Chemistry B
Print ISSN 1520-6106
Electronic ISSN 1520-5207
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 109
Issue 1
Pages 652-661
DOI https://doi.org/10.1021/jp0402434
Keywords Materials Chemistry; Surfaces, Coatings and Films; Physical and Theoretical Chemistry