Solid-state NMR characterisation of the thermal transformation of a Hungarian white illite
1H, 27Al, 29Si and 39K solid-state NMR are reported from a Hungarian illite 2:1 clay for samples heated up 1600 °C. This single-phase sample has a small amount of aluminium substitution in the silica layer and very low iron-content (∼0.4 wt%). Thermal analysis shows several events that can be relate...
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container_title | Solid state nuclear magnetic resonance |
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creator | Carroll, D.L. Kemp, T.F. Bastow, T.J. Smith, M.E. |
description | 1H,
27Al,
29Si and
39K solid-state NMR are reported from a Hungarian illite 2:1 clay for samples heated up 1600
°C. This single-phase sample has a small amount of aluminium substitution in the silica layer and very low iron-content (∼0.4
wt%). Thermal analysis shows several events that can be related to features in the NMR spectra, and hence changes in the atomic scale structure. As dehydroxylation occurs there is increasing AlO
4 and AlO
5-contents. The silica and gibbsite layers become increasingly separated as the dehydroxylation progresses. Between 900 and 1000
°C the silica layer forms a potassium aluminosilicate glass. The gibbsite-layer forms spinel/
γ-Al
2O
3 and some aluminium-rich mullite. Then on heating to 1600
°C changes in the
29Si and
27Al MAS NMR spectra are consistent with the aluminosilicate glass increasing its aluminium-content, the amount of mullite increasing probably with its silicon-content also increasing, and some
α-Al
2O
3 forming. |
doi_str_mv | 10.1016/j.ssnmr.2005.04.001 |
format | Article |
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27Al,
29Si and
39K solid-state NMR are reported from a Hungarian illite 2:1 clay for samples heated up 1600
°C. This single-phase sample has a small amount of aluminium substitution in the silica layer and very low iron-content (∼0.4
wt%). Thermal analysis shows several events that can be related to features in the NMR spectra, and hence changes in the atomic scale structure. As dehydroxylation occurs there is increasing AlO
4 and AlO
5-contents. The silica and gibbsite layers become increasingly separated as the dehydroxylation progresses. Between 900 and 1000
°C the silica layer forms a potassium aluminosilicate glass. The gibbsite-layer forms spinel/
γ-Al
2O
3 and some aluminium-rich mullite. Then on heating to 1600
°C changes in the
29Si and
27Al MAS NMR spectra are consistent with the aluminosilicate glass increasing its aluminium-content, the amount of mullite increasing probably with its silicon-content also increasing, and some
α-Al
2O
3 forming.</description><identifier>ISSN: 0926-2040</identifier><identifier>EISSN: 1527-3326</identifier><identifier>DOI: 10.1016/j.ssnmr.2005.04.001</identifier><identifier>PMID: 15899582</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Clay mineral ; Dehydroxylation ; Illite ; Solid-state NMR ; Thermal processing</subject><ispartof>Solid state nuclear magnetic resonance, 2005-07, Vol.28 (1), p.31-43</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-385f5b6becab31458227cc033a6bac28ba51e07deb576d1e0b670152a93a68d33</citedby><cites>FETCH-LOGICAL-c433t-385f5b6becab31458227cc033a6bac28ba51e07deb576d1e0b670152a93a68d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ssnmr.2005.04.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15899582$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carroll, D.L.</creatorcontrib><creatorcontrib>Kemp, T.F.</creatorcontrib><creatorcontrib>Bastow, T.J.</creatorcontrib><creatorcontrib>Smith, M.E.</creatorcontrib><title>Solid-state NMR characterisation of the thermal transformation of a Hungarian white illite</title><title>Solid state nuclear magnetic resonance</title><addtitle>Solid State Nucl Magn Reson</addtitle><description>1H,
27Al,
29Si and
39K solid-state NMR are reported from a Hungarian illite 2:1 clay for samples heated up 1600
°C. This single-phase sample has a small amount of aluminium substitution in the silica layer and very low iron-content (∼0.4
wt%). Thermal analysis shows several events that can be related to features in the NMR spectra, and hence changes in the atomic scale structure. As dehydroxylation occurs there is increasing AlO
4 and AlO
5-contents. The silica and gibbsite layers become increasingly separated as the dehydroxylation progresses. Between 900 and 1000
°C the silica layer forms a potassium aluminosilicate glass. The gibbsite-layer forms spinel/
γ-Al
2O
3 and some aluminium-rich mullite. Then on heating to 1600
°C changes in the
29Si and
27Al MAS NMR spectra are consistent with the aluminosilicate glass increasing its aluminium-content, the amount of mullite increasing probably with its silicon-content also increasing, and some
α-Al
2O
3 forming.</description><subject>Clay mineral</subject><subject>Dehydroxylation</subject><subject>Illite</subject><subject>Solid-state NMR</subject><subject>Thermal processing</subject><issn>0926-2040</issn><issn>1527-3326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkE1P3DAQhq2qqCyUX1AJ5dRbwtiOneTQA0LlQ6JFgnLhYk2cSderfIDtLeLf42UX9dYerBnJz7xjP4x94VBw4PpkVYQwjb4QAKqAsgDgH9iCK1HlUgr9kS2gEToXUMI-OwhhBQAVl_oT2-eqbhpViwV7uJsH1-UhYqTs54_bzC7Ro43kXcDo5imb-ywuaXP8iEMWPU6hn1P_fovZ5Xr6jd7hlD0vXcpxw5DKZ7bX4xDoaFcP2f35919nl_n1zcXV2el1bkspYy5r1atWt2SxlbxMrxKVtSAl6hatqFtUnKDqqFWV7lLb6grSL7FJRN1Jeci-bnMf_fy0phDN6IKlYcCJ5nUwugalmlL8FxRJScpuEii3oPVzCJ568-jdiP7FcDAb92Zl3tybjXsDpUnu09TxLn7djtT9ndnJTsC3LUDJxh9H3gTraLLUOU82mm52_1zwCksJlwg</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Carroll, D.L.</creator><creator>Kemp, T.F.</creator><creator>Bastow, T.J.</creator><creator>Smith, M.E.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Solid-state NMR characterisation of the thermal transformation of a Hungarian white illite</title><author>Carroll, D.L. ; Kemp, T.F. ; Bastow, T.J. ; Smith, M.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-385f5b6becab31458227cc033a6bac28ba51e07deb576d1e0b670152a93a68d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Clay mineral</topic><topic>Dehydroxylation</topic><topic>Illite</topic><topic>Solid-state NMR</topic><topic>Thermal processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carroll, D.L.</creatorcontrib><creatorcontrib>Kemp, T.F.</creatorcontrib><creatorcontrib>Bastow, T.J.</creatorcontrib><creatorcontrib>Smith, M.E.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Solid state nuclear magnetic resonance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carroll, D.L.</au><au>Kemp, T.F.</au><au>Bastow, T.J.</au><au>Smith, M.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solid-state NMR characterisation of the thermal transformation of a Hungarian white illite</atitle><jtitle>Solid state nuclear magnetic resonance</jtitle><addtitle>Solid State Nucl Magn Reson</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>28</volume><issue>1</issue><spage>31</spage><epage>43</epage><pages>31-43</pages><issn>0926-2040</issn><eissn>1527-3326</eissn><abstract>1H,
27Al,
29Si and
39K solid-state NMR are reported from a Hungarian illite 2:1 clay for samples heated up 1600
°C. This single-phase sample has a small amount of aluminium substitution in the silica layer and very low iron-content (∼0.4
wt%). Thermal analysis shows several events that can be related to features in the NMR spectra, and hence changes in the atomic scale structure. As dehydroxylation occurs there is increasing AlO
4 and AlO
5-contents. The silica and gibbsite layers become increasingly separated as the dehydroxylation progresses. Between 900 and 1000
°C the silica layer forms a potassium aluminosilicate glass. The gibbsite-layer forms spinel/
γ-Al
2O
3 and some aluminium-rich mullite. Then on heating to 1600
°C changes in the
29Si and
27Al MAS NMR spectra are consistent with the aluminosilicate glass increasing its aluminium-content, the amount of mullite increasing probably with its silicon-content also increasing, and some
α-Al
2O
3 forming.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>15899582</pmid><doi>10.1016/j.ssnmr.2005.04.001</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
recordid | cdi_proquest_miscellaneous_68055942 |
source | Access via ScienceDirect (Elsevier) |
subjects | Clay mineral Dehydroxylation Illite Solid-state NMR Thermal processing |
title | Solid-state NMR characterisation of the thermal transformation of a Hungarian white illite |
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