Physico-chemical characterization of Cu2+-exchanged sepiolite
- 1 December 1985
- journal article
- Published by Mineralogical Society in Clay Minerals
- Vol. 20 (4) , 467-475
- https://doi.org/10.1180/claymin.1985.020.4.03
Abstract
Copper-sepiolites exchanged at different levels have been studied by ESR, IR, and TG. The results indicate that in the unheated samples the Cu2+ ions are located in octahedral edge positions. After dehydration, the Cu2+ ions occur in two positions with different environments. Some of the Cu2+ ions lose the two molecules of coordinated water in one step, at low dehydration temperatures, and adopt a square pyramidal geometry. Other Cu2+ ions lose the coordination water in two steps, at lower temperature than the natural sepiolite, and adopt a tetrahedral symmetry.Keywords
This publication has 11 references indexed in Scilit:
- Surface acidity and catalytic activity of a modified sepioliteClay Minerals, 1984
- Crystal field theory and EPR parameters in D2d and C2v distorted tetrahedral copper(II) complexesJournal of Solid State Chemistry, 1982
- Hydrolysis and Dehydration Reactions of Exchangeable Cu2+ on HectoriteClays and Clay Minerals, 1982
- Electron spin resonance of copper-exchanged Y zeolites. Part 1.—Behaviour of the cation during dehydrationJournal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1979
- Electron spin resonance studies of cation orientation in restricted water layers on phyllosilicate (smectite) surfacesThe Journal of Physical Chemistry, 1975
- Folding in Sepiolite CrystalsClays and Clay Minerals, 1975
- On Dehydration of Bound Water of SepioliteClays and Clay Minerals, 1974
- Further electron spin resonance studies of Cu(II) in Linde Y zeolite*1Journal of Catalysis, 1972
- The electronic properties and stereochemistry of mono-nuclear complexes of the copper(II) ionCoordination Chemistry Reviews, 1970
- Sorption by Attapulgite. II. Selectivity Shown by Attapulgite, Sepiolite and Montmorillonite for n-ParaffinsThe Journal of Physical Chemistry, 1954