z-logo
Premium
The Hydrothermal Synthesis of Petalite Mineral Phases and their Morphological Changing by Increasing of Temperature
Author(s) -
Ghobarkar Habib
Publication year - 1992
Publication title -
crystal research and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.377
H-Index - 64
eISSN - 1521-4079
pISSN - 0232-1300
DOI - 10.1002/crat.2170270403
Subject(s) - tetragonal crystal system , orthorhombic crystal system , materials science , chemistry , crystallography , mineralogy , crystal structure
In this investigation the Petalite minerals were synthesized hydrothermally at different temperatures from a glass with the composition Li 2 CO 3 :Al 2 O 3 : SiO 2 and the relation 1: 1: 8. On that occasion the following mineral phases arised:at low temperatures (410°C) α‐petalite (unit cell å = 11.737 Å/b̊ = 5.17 Å/c̊ = 7.63 Å, space group P 2 /a); At 490 °C α‐petalite was splitted to quartz and an orthorhombic β 1 ‐petalite (unit cell å = 18.24 Å/c̊ = 10.54 Å/c̊ = 10.57 Å, space group P m C n ). β 1 ‐petalite could be observated until 1000 °C. at 560 °C tetragonal β 2 ‐petalite (unit cell å = 7.50 Å/c̊ = 9.07 Å, space group P 4 3 2 1 2) in parallel with β 1 ‐petalite; Behind 750 °C β 2 ‐petalite was not observed. Behind 900 °C a pseudohexagonal mineral phase developed from β 1 ‐petalite. May be it is possible to indicate this phase as hexagonal (unit cell å = 5.217 Å/c̊ = 5.464 Å, space group P 6 2 22 or P 6 4 22). The author suggests to denote this phase as β 3 ‐petalite.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom