Abstract
A new superstructure was found in mordenite (Na5.59Ca1.80Al9.19Si38.81O96·nH2O) from Challis Valley, Idaho-a zeolite widely used in previous studies. The occurrence of the superstructure reflections were observed in 12 specimens from two rock samples, at the midpoint of layers in the oscillation photographs around the a* and b* axes, but not around the c* axis. The apparent 2a, 2b, and c axes are orthogonal. In spite of yielding an apparent orthorhombic cell, careful observation of the intensities revealed that the superstructure is monoclinic with twice the volume of the orthorhombic cell: a’ = 27.356(9), b’ = 27.356(9), c’ = 7.517(2) Å, γ′ = 97.14(4)°, and V′ = 5582(4) Å3.
The presence of the superstructure was examined for specimens from ten other localities and a synthetic sample but there was no evidence for extra spots of the superstructure, indicating that the occurrence is not common.
The large displacement factors of O8 oxygen, and its associated 180° T-O-T angle that is energetically unfavorable, are basic to the mordenite structure. In the monoclinic superstructure the O8 oxygen is decomposed into several asymmetric O atoms by the symmetry reduction. The large displacement smearing of O8 oxygen perpendicular to the straight T-O-T, are explained by the superposition of decomposed O atoms.
The extra spots are predominantly observed in the reciprocal planes with l = odd in the same way as diffuse streaks. The observation of extra spots and diffuse streaks suggests that there are three kinds of domains in the mordenite, one in the ordered form and two others in the random form of c/2 linear displacements. The domain in the ordered form represents the superstructure. Thus, we propose a model for the superstructure in which the c/2 displacement occurs alternatively in the two basic unit cells slightly modified in the superstructure, yielding the periodic arrangements.
© 2015 by Walter de Gruyter Berlin/Boston
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- An infrared investigation of the otavite-magnesite solid solution
- Partitioning of calcium, magnesium, and transition metals between olivine and melt governed by the structure of the silicate melt at ambient pressure
- The geometric effects of VFe2+ for VMg substitution on the crystal structures of the grandidierite-ominelite series
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Articles in the same Issue
- Single-crystal FTIR and X-ray study of vishnevite, ideally [Na6(SO4)][Na2(H2O)2](Si6Al6O24)
- Crystallographic texture and microstructure of terebratulide brachiopod shell calcite: An optimized materials design with hierarchical architecture
- High-temperature phase relations and topological constraints in the quaternary system MgO-Al2O3-SiO2-Cr2O3: An experimental study
- Tilt and buckling modes, and acoustic anisotropy in layers with post-perovskite connectivity
- Optical absorption study of natural garnets of almandine-skiagite composition showing intervalence Fe2+ + Fe3+ → Fe3+ + Fe2+ charge-transfer transition
- Deriving formation constants for aqueous metal complexes from XANES spectra: Zn2+ and Fe2+ chloride complexes in hypersaline solutions
- Birnessite polytype systematics and identiÞ cation by powder X-ray diffraction
- Improved measurement of fission-track annealing in apatite using c-axis projection
- Improved modeling of fission-track annealing in apatite
- Intercalibration of FTIR and SIMS for hydrogen measurements in glasses and nominally anhydrous minerals
- Order and miscibility in the otavite–magnesite solid solution
- An infrared investigation of the otavite-magnesite solid solution
- Partitioning of calcium, magnesium, and transition metals between olivine and melt governed by the structure of the silicate melt at ambient pressure
- The geometric effects of VFe2+ for VMg substitution on the crystal structures of the grandidierite-ominelite series
- The iron oxidation state of garnet by electron microprobe: Its determination with the flank method combined with major-element analysis
- Gram-Charlier development of the atomic displacement factors into mineral structures: The case of samsonite, Ag4MnSb2S6
- Superstructure of Challis mordenite with doubled monoclinic unit cell
- Biopyribole evolution during tremolite synthesis from dolomite and quartz in CO2-H2O fluid
- The evolution of diamond morphology in the process of dissolution: Experimental data
- The pearceite-polybasite group of minerals: Crystal chemistry and new nomenclature rules
- Determination of layer stacking microstructures and intralayer transition of illite polytypes by high-resolution transmission electron microscopy (HRTEM)
- Structural behavior of Al3+ in peralkaline, metaluminous, and peraluminous silicate melts and glasses at ambient pressure
- The crystal structure of ingersonite, Ca3Mn2+Sb45+O14, and its relationships with pyrochlore
- Chemical composition, statistical analysis of the unit cell, and electrostatic modeling of the structure of Al-saturated chlorite from metamorphosed rocks
- XANES study of the oxidation state of Cr in lower mantle phases: Periclase and magnesium silicate perovskite
- Crystal chemistry of hydration in aluminous orthopyroxene