Structural transformation of 2:1 dioctahedral layer silicates during dehydroxylation-rehydroxylation reactions

The structural transformation of dioctahedral 2:1 layer silicates (illite, montmorillonite, glauconite, and celadonite) during a dehydoxylation-rehydroxylation process has been studied by X-ray diffraction, thermal analysis, and infrared spectroscopy. The layers of the samples differ in the distribu...

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Veröffentlicht in:Clays and clay minerals 2000-10, Vol.48 (5), p.572-585
Hauptverfasser: Muller, Fabrice, Drits, Victor, Plançon, Alain, Robert, Jean-Louis
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Drits, Victor
Plançon, Alain
Robert, Jean-Louis
description The structural transformation of dioctahedral 2:1 layer silicates (illite, montmorillonite, glauconite, and celadonite) during a dehydoxylation-rehydroxylation process has been studied by X-ray diffraction, thermal analysis, and infrared spectroscopy. The layers of the samples differ in the distribution of the octahedral cations over the cis- and trans-sites as determined by the analysis of the positions and intensities of the 11l, 02l reflections, and that of the relative displacements of adjacent layers along the a axis (c cos β/a), as well as by dehydroxylation-temperature values. One illite, glauconite, and celadonite consist of trans-vacant (tv) layers; Wyoming montmorillonite is composed of cis-vacant (cv) layers, where-as in the other illite sample tv and cv layers are interstratified. The results obtained show that the rehydroxylated Al-rich minerals (montmorillonite, illites) consist of tv layers whatever the distribution of octahedral cations over cis- and trans-sites in the original structure. The reason for this is that in the dehydroxylated state, both tv and cv layers are transformed into the same layer structure where the former trans-sites are vacant. The dehydroxylation of glauconite and celadonite is accompanied by a migration of the octahedral cations from former cis-octahedra to empty trans-sites. The structural transformation of these minerals during rehydroxylation depends probably on their cation composition. The rehydroxylation of celadonite preserves the octahedral-cation distribution formed after dehydroxylation. Therefore, most 2:1 layers of celadonite that rehydroxylate (∼75%) have cis-vacant octahedra and, only in a minor part of the layers, a reverse cation migration from former trans-sites to empty octahedra occurred. In contrast, for a glauconite sample with a high content in IVAl and VIAl the rehydroxylation is accompanied by the reverse cation migration and most of the 2:1 layers are transformed into tv layers.
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The layers of the samples differ in the distribution of the octahedral cations over the cis- and trans-sites as determined by the analysis of the positions and intensities of the 11l, 02l reflections, and that of the relative displacements of adjacent layers along the a axis (c cos β/a), as well as by dehydroxylation-temperature values. One illite, glauconite, and celadonite consist of trans-vacant (tv) layers; Wyoming montmorillonite is composed of cis-vacant (cv) layers, where-as in the other illite sample tv and cv layers are interstratified. The results obtained show that the rehydroxylated Al-rich minerals (montmorillonite, illites) consist of tv layers whatever the distribution of octahedral cations over cis- and trans-sites in the original structure. The reason for this is that in the dehydroxylated state, both tv and cv layers are transformed into the same layer structure where the former trans-sites are vacant. The dehydroxylation of glauconite and celadonite is accompanied by a migration of the octahedral cations from former cis-octahedra to empty trans-sites. The structural transformation of these minerals during rehydroxylation depends probably on their cation composition. The rehydroxylation of celadonite preserves the octahedral-cation distribution formed after dehydroxylation. Therefore, most 2:1 layers of celadonite that rehydroxylate (∼75%) have cis-vacant octahedra and, only in a minor part of the layers, a reverse cation migration from former trans-sites to empty octahedra occurred. 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The layers of the samples differ in the distribution of the octahedral cations over the cis- and trans-sites as determined by the analysis of the positions and intensities of the 11l, 02l reflections, and that of the relative displacements of adjacent layers along the a axis (c cos β/a), as well as by dehydroxylation-temperature values. One illite, glauconite, and celadonite consist of trans-vacant (tv) layers; Wyoming montmorillonite is composed of cis-vacant (cv) layers, where-as in the other illite sample tv and cv layers are interstratified. The results obtained show that the rehydroxylated Al-rich minerals (montmorillonite, illites) consist of tv layers whatever the distribution of octahedral cations over cis- and trans-sites in the original structure. The reason for this is that in the dehydroxylated state, both tv and cv layers are transformed into the same layer structure where the former trans-sites are vacant. The dehydroxylation of glauconite and celadonite is accompanied by a migration of the octahedral cations from former cis-octahedra to empty trans-sites. The structural transformation of these minerals during rehydroxylation depends probably on their cation composition. The rehydroxylation of celadonite preserves the octahedral-cation distribution formed after dehydroxylation. Therefore, most 2:1 layers of celadonite that rehydroxylate (∼75%) have cis-vacant octahedra and, only in a minor part of the layers, a reverse cation migration from former trans-sites to empty octahedra occurred. 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Drits, Victor ; Plançon, Alain ; Robert, Jean-Louis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a410t-ce36c224343d324b64ec0fa8872e866a9348c1f3c26ce6a82c34161deff4c1ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>celadonite</topic><topic>chemical properties</topic><topic>chemical reactions</topic><topic>Chemical Sciences</topic><topic>clay mineralogy</topic><topic>clay minerals</topic><topic>crystal structure</topic><topic>dehydroxylation</topic><topic>Earth Sciences</topic><topic>experimental studies</topic><topic>Geochemistry</topic><topic>glauconite</topic><topic>illite</topic><topic>infrared spectra</topic><topic>Material chemistry</topic><topic>mica group</topic><topic>mixed-layer minerals</topic><topic>montmorillonite</topic><topic>polyhedra</topic><topic>rehydroxylation</topic><topic>rock, sediment, soil</topic><topic>Sciences of the Universe</topic><topic>sed rocks, sediments</topic><topic>Sedimentary petrology</topic><topic>sheet silicates</topic><topic>silicates</topic><topic>smectite</topic><topic>spectra</topic><topic>X-ray diffraction data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muller, Fabrice</creatorcontrib><creatorcontrib>Drits, Victor</creatorcontrib><creatorcontrib>Plançon, Alain</creatorcontrib><creatorcontrib>Robert, Jean-Louis</creatorcontrib><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Clays and clay minerals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muller, Fabrice</au><au>Drits, Victor</au><au>Plançon, Alain</au><au>Robert, Jean-Louis</au><au>WCA</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural transformation of 2:1 dioctahedral layer silicates during dehydroxylation-rehydroxylation reactions</atitle><jtitle>Clays and clay minerals</jtitle><date>2000-10-01</date><risdate>2000</risdate><volume>48</volume><issue>5</issue><spage>572</spage><epage>585</epage><pages>572-585</pages><issn>0009-8604</issn><eissn>1552-8367</eissn><abstract>The structural transformation of dioctahedral 2:1 layer silicates (illite, montmorillonite, glauconite, and celadonite) during a dehydoxylation-rehydroxylation process has been studied by X-ray diffraction, thermal analysis, and infrared spectroscopy. The layers of the samples differ in the distribution of the octahedral cations over the cis- and trans-sites as determined by the analysis of the positions and intensities of the 11l, 02l reflections, and that of the relative displacements of adjacent layers along the a axis (c cos β/a), as well as by dehydroxylation-temperature values. One illite, glauconite, and celadonite consist of trans-vacant (tv) layers; Wyoming montmorillonite is composed of cis-vacant (cv) layers, where-as in the other illite sample tv and cv layers are interstratified. The results obtained show that the rehydroxylated Al-rich minerals (montmorillonite, illites) consist of tv layers whatever the distribution of octahedral cations over cis- and trans-sites in the original structure. The reason for this is that in the dehydroxylated state, both tv and cv layers are transformed into the same layer structure where the former trans-sites are vacant. The dehydroxylation of glauconite and celadonite is accompanied by a migration of the octahedral cations from former cis-octahedra to empty trans-sites. The structural transformation of these minerals during rehydroxylation depends probably on their cation composition. The rehydroxylation of celadonite preserves the octahedral-cation distribution formed after dehydroxylation. Therefore, most 2:1 layers of celadonite that rehydroxylate (∼75%) have cis-vacant octahedra and, only in a minor part of the layers, a reverse cation migration from former trans-sites to empty octahedra occurred. In contrast, for a glauconite sample with a high content in IVAl and VIAl the rehydroxylation is accompanied by the reverse cation migration and most of the 2:1 layers are transformed into tv layers.</abstract><pub>Clay Minerals Society</pub><doi>10.1346/ccmn.2000.0480510</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-2147-4101</orcidid><oa>free_for_read</oa></addata></record>
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source SpringerNature Journals
subjects celadonite
chemical properties
chemical reactions
Chemical Sciences
clay mineralogy
clay minerals
crystal structure
dehydroxylation
Earth Sciences
experimental studies
Geochemistry
glauconite
illite
infrared spectra
Material chemistry
mica group
mixed-layer minerals
montmorillonite
polyhedra
rehydroxylation
rock, sediment, soil
Sciences of the Universe
sed rocks, sediments
Sedimentary petrology
sheet silicates
silicates
smectite
spectra
X-ray diffraction data
title Structural transformation of 2:1 dioctahedral layer silicates during dehydroxylation-rehydroxylation reactions
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