Pressure-induced symmetry changes in body-centred cubic zeolites

Previous work has shown a strong correlation between zeolite framework flexibility and the nature of structural symmetry and phase transitions. However, there is little experimental data regarding this relationship, in addition to how flexibility can be connected to the synthesis of these open-frame...

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Published inRoyal Society open science Vol. 6; no. 7; p. 182158
Main Authors Nearchou, Antony, Cornelius, Mero-Lee U, Jones, Zöe L, Collings, I E, Wells, Stephen A, Raithby, Paul R, Sartbaeva, Asel
Format Journal Article
LanguageEnglish
Published England The Royal Society 01.07.2019
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Summary:Previous work has shown a strong correlation between zeolite framework flexibility and the nature of structural symmetry and phase transitions. However, there is little experimental data regarding this relationship, in addition to how flexibility can be connected to the synthesis of these open-framework materials. This is of interest for the synthesis of novel zeolites, which require organic additives to permutate the resulting geometry and symmetry of the framework. Here, we have used high-pressure powder X-ray diffraction to study the three zeolites: Na-X, RHO and ZK-5, which can all be prepared using 18-crown-6 ether as an organic additive. We observe significant differences in how the occluded 18-crown-6 ether influences the framework flexibility-this being dependent on the geometry of the framework. We use these differences as an indicator to define the role of 18-crown-6 ether during zeolite crystallization. Furthermore, in conjunction with previous work, we predict that pressure-induced symmetry transitions are intrinsic to body-centred cubic zeolites. The high symmetry yields fewer degrees of freedom, meaning it is energetically favourable to lower the symmetry to facilitate further compression.
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This article has been edited by the Royal Society of Chemistry, including the commissioning, peer review process and editorial aspects up to the point of acceptance.
Electronic supplementary material is available online at https://dx.doi.org/10.6084/m9.figshare.c.4570970.
ISSN:2054-5703
2054-5703
DOI:10.1098/rsos.182158