Download | - View final version: Contribution to the crystal chemistry of the layer silicates (PDF, 1.2 MiB)
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DOI | Resolve DOI: https://doi.org/10.4224/20375702 |
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Author | Search for: Liebau, F.; Search for: National Research Council of Canada. Division of Building Research |
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Format | Text, Technical Report |
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Physical description | 23 p. |
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Subject | silicate minerals; crystalline state; cations |
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Abstract | The great number of (Si[2]O[5]) layer silicates is primarily due to the differences in size and charge of the cations. Anhydrous layer silicates show an increasing degree of convolution of layers with decreasing radius/charge ratio of cations, the size of cation sites between layers decreasing at the same time. This explains why 1+ cations form anhydrous layer silicates and 2+ cations of small or medium size and 3+ cations do not. In hydrous layer silicates the [ MeO(OH)] polyhedra are `effective' cations. The deviation from a plain conformation increases with increasing ratio radius/charge, from Al[4](Si[4]O[10])(OH)[8] and the bent serpentines to the ruffled ones of pyrosmalite and apophyllite. |
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Publication date | 1971 |
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Publisher | National Research Council of Canada |
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Series | |
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Language | English |
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Peer reviewed | No |
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NRC number | NRC-IRC-524 |
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NPARC number | 20375702 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | fa8877a1-26b8-4160-aaae-f6c6b5646567 |
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Record created | 2012-07-23 |
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Record modified | 2023-01-24 |
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