Clays and clay minerals (National Conference on Clays and Clay Minerals) · 1958 · 34 citations · 9 references
Natural SciencesChemistryMaterials ScienceCrystal StructureInorganic ChemistrySoil-water RelationsClay MineralogyWater ChemistryWater RelationsBondingExchangeable BondsInfrared Absorption SpectroscopyThermogravimetric CurvesThermogravimetric Data AnalysisUnit Cell ParametersUnit Cell SymmetryVermiculite Minerals
Abstract Selected chemical and diffraction analyses from the literature, supplemented by thermal and thermogravimetric analyses and infrared absorption observations, are utilized to construct a rational model of the water arrangement in natural vermiculites. A super cell is arranged by simple modification of the Hendricks water nets to accommodate the somewhat higher water contents, indicated by weight loss analyses, and the exchangeable cations. A three-cell unit (15.6 × 9 Å) contains two Mg 2+ ·6H 2 O octahedra centered at the corners and face centers and four 4H 2 O squares centered about ±5.2 Å along a between the octahedra. The arrangement affords twenty hydrogen bonds near 2.75 Å, twelve between silicate and water layers and eight between water layers, and thirty-two hydrogen bonds near 3.0 Å within water layers. The remaining four hydrogens are not active in the bonding system. The environment of each water molecule is a distorted tetrahedron. A broad infrared absorption band shows maxima at about 3600, 3450 and 3350 cm −1 at normal incidence, with increased activity in the highest and lowest energies when a flake is tilted. It is concluded that OH axes in the shortest bonds are more inclined to the cleavage planes than are the intermediate length axes.
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Crystal structure of magnesium-vermiculite
A. McL Mathieson, G. F. Walker · American Mineralogist · 1954 · 153 citations
George L. Clark · Journal of the American Chemical Society · 1959 · 132 citations