“Pressure-Induced Hydration and Order-Disorder Transition in a Synthetic Potassium Gallosilicate Zeolite with Gismondine Topology”
Y. Lee*, S.J. Kim, C.-C. Kao, and T. Vogt
Journal of the American Chemical Society
Vol.130, No.9, pp.2842-2850, 2008.03
Two high-pressure phases of a potassium gallosilicate with a gismondine framework (K−GaSi-GIS) were characterized using Rietveld refinements of in-situ high-pressure, high-resolution synchrotron X-ray powder diffraction data. The observed response of the K−GaSi-GIS framework under hydrostatic pressure is a gradual flattening of the so-called “double crankshaft” structural chain units. At pressures below 1.0(1) GPa, additional water molecules from the hydrostatic pressure-transmitting medium are inserted into the potassium-water guest network (“pressure-induced hydration”) resulting in a “super-hydrated” high-pressure phase I. As the flattening of the double crankshaft structural units in the GIS framework continues above 1.6 GPa, the ellipticity of the cross-linking 8-ring windows is reduced below a certain threshold, and a disordering of the potassium-water guest structure along the 8-ring channel, characteristic of a disordered high-pressure phase II, is observed. The concerted framework distortion and guest network disordering accommodates the increased hydration level while maintaining the seven-fold coordination environment of the potassium cations to framework oxygen atoms and water molecules. We have thus established the atomistic details of a guest−host order−disorder transition under pressure-induced hydration conditions in a zeolite with GIS framework and compared it to other zeolites during pressure-induced hydration. We find that the structural changes mediated by the extra-framework cations and their coordination environment under PIH conditions are at the core of these different mechanisms and are driving the changes in the ellipticity of pore openings, order−disorder and disorder−order transitions, and framework distortions.