An X-ray diffraction refinement of the crystal structure of natural orthorhombic analcime (NaAlSi2O6·H2O)
✍ Scribed by F. Pechar
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 204 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0144-2449
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✦ Synopsis
of Geology and Geotechnics, V Holegovi(k(zch An X-ray diffraction analysis was performed on a single crystal of natural orthorhombic analcime: (Nao.s6Ko.o6 Cao.os) [(AI0.ssFeomSi2.osTio.ol)O6]-1.12 H20; Ibca: a = 13.720(2) A, b = 13.715(2) /~, c = 13.709(1)/~; V = 2579.8/~3; Z = 16 (locality: Vl6f Hora, Bohemia). Refinement of 1340 independent reflections yields R = 0.032. The mean Si(AI)-0 distance is 1.6467 /~, and the angle is 109.49 °. The framework of orthorhombic analcime is topologically the same as cubic modification.
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An X-ray Diffraction Refinement of the Crystal Structure of Natural Stellerite, Ca(A18Sies)0,e 28 HaO An X-ray diffraction analysis was performed on a single crystal of natural stellerite, (Ca3.ssN~o.3sKo.osMgo.oe)tot. 4.06 (Al7.88Feo.o~)t~t. =7.97Si28.o2O7, . 38.25 H,O, orthorhombic, Fmmm, a = 13.6