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Title: Anisotropic compression of a synthetic potassium aluminogermanate zeolite with gismondine topology

Journal Article · · Journal of Solid State Chemistry

Compression behavior of a potassium aluminogermanate with a gismondine framework topology (K-AlGe-GIS) was studied using in-situ high-pressure synchrotron X-ray powder diffraction. In contrast to the potassium gallosilicate analogue (K-GaSi-GIS), no elastic anomaly due to pressure-induced hydration and/or cation relocation was observed in K-AlGe-GIS. The Birch-Murnaghan fit to the pressure-volume data results in a bulk modulus of B{sub 0} = 31(1) GPa. The derived linear-axial compressibilities (i.e., {beta}{sub a} = 0.0065(5) GPa{sup -1}, {beta}{sub b} = 0.0196(4) GPa{sup -1}, {beta}{sub c} = 0.0081(7) GPa{sup -1}) indicate that the b-axis, normal to the 8-ring channels, is about three times more compressible than the a and c axes, parallel to the elliptical 8-ring channels. As a consequence a gradual flattening of the so-called 'double crankshaft' structural building units of the gismondine framework is observed. In K-AlGe-GIS, this flattening occurs almost linear with pressure, whereas it is nonlinear in the GaSi-analogue due to structural changes of the water-cation assembly under hydrostatic pressures.

Research Organization:
Brookhaven National Lab. (BNL), Upton, NY (United States)
Sponsoring Organization:
DOE - Office Of Science
DOE Contract Number:
DE-AC02-98CH10886
OSTI ID:
991726
Report Number(s):
BNL-94181-2010-JA; JSSCBI; R&D Project: LS001; KC0401030; TRN: US1007550
Journal Information:
Journal of Solid State Chemistry, Vol. 183, Issue 10; ISSN 0022-4596
Country of Publication:
United States
Language:
English