The effect of solid solution on the stability of talc and 10-Å phase
Talc and 10-Å phase are hydrous phases that are implicated in fluid processes and rheological behaviour in subduction zones. Natural samples of talc show limited compositional variation away from the MgO–SiO 2 –H 2 O (MSH) endmember, with only substitution of Fe 2+ for Mg occurring in significant am...
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description | Talc and 10-Å phase are hydrous phases that are implicated in fluid processes and rheological behaviour in subduction zones. Natural samples of talc show limited compositional variation away from the MgO–SiO
2
–H
2
O (MSH) endmember, with only substitution of Fe
2+
for Mg occurring in significant amounts. In experiments at 2 GPa, talc containing 0.48 apfu Fe
2+
begins to break down in the divariant field talc + anthophyllite + quartz at ~ 550 °C, a temperature ~ 270 °C lower than in the MSH system. At 4 GPa, Fe-bearing talc breaks down over a wide temperature interval in the divariant field talc + enstatite + coesite. The large decrease in temperature of the beginning of talc breakdown shows that Fe
2+
is partitioned strongly into enstatite and anthophyllite with respect to talc. In phase reversal experiments at 6.5 GPa, the beginning of the dehydration of 10-Å phase containing 0.48 apfu Fe
2+
was bracketed between 575 °C and 600 °C, a temperature ~ 100 °C lower than the MSH endmember reaction. The relative positions of the talc and 10-Å phase dehydration reactions indicate that the latter is able to accommodate greater Fe substitution, and is, therefore, more stable in Fe-bearing systems. In experiments at 6.2 GPa, 650 °C in the systems MgO–Al
2
O
3
–SiO
2
–H
2
O (MASH) and Na
2
O–MgO–Al
2
O
3
–SiO
2
–H
2
O (NMASH), 10-Å phase was synthesised that contains up to 0.5 apfu Al in the system MASH (compared to 0.8 in the starting material) and up to 0.4 apfu Al + 0.4 apfu Na in the system NMASH (compared to 0.7 of each of Al and Na in the starting material). Further experiments are required to determine if higher Al and Na contents in 10-Å phase are possible. The much higher Al and Na contents than found in talc indicate that, as with Fe, substitution of these elements enlarges the 10-Å phase stability field with respect to talc. In contrast to the effect of Fe, Al and Na also increase the stability of 10-Å phase relative to its thermal breakdown products enstatite + coesite. |
doi_str_mv | 10.1007/s00410-019-1616-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2294876422</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2294876422</sourcerecordid><originalsourceid>FETCH-LOGICAL-a2970-f27fbe5ef12e65bcacb91f5f3e8fe297780a8276c050b1b50378a13576b989a73</originalsourceid><addsrcrecordid>eNp1kM9KAzEQxoMoWKsP4C3gOTrJbv4dpVQrFLzUc0i2id2y7tYkPfQBfDJfzCwreBKGGYb5fd_Ah9AthXsKIB8SQE2BANWECioInKEZrStGQAt5jmYA5Sq11pfoKqU9lF1pPkPLzc5jH4JvMh4CTkPXbsd-zO3Q41K53FO2ru3afBqRbLsG236Li-H3Fz7sbPLX6CLYLvmb3zlHb0_LzWJF1q_PL4vHNbFMSyCByeA894EyL7hrbOM0DTxUXgVfCKnAKiZFAxwcdRwqqSytuBROK21lNUd3k-8hDp9Hn7LZD8fYl5eGMV0rKWrGCkUnqolDStEHc4jth40nQ8GMaZkpLVPSMmNaBoqGTZpU2P7dxz_n_0U_IDdrAA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2294876422</pqid></control><display><type>article</type><title>The effect of solid solution on the stability of talc and 10-Å phase</title><source>SpringerLink Journals - AutoHoldings</source><creator>Howe, Harriet ; Pawley, Alison R.</creator><creatorcontrib>Howe, Harriet ; Pawley, Alison R.</creatorcontrib><description>Talc and 10-Å phase are hydrous phases that are implicated in fluid processes and rheological behaviour in subduction zones. Natural samples of talc show limited compositional variation away from the MgO–SiO
2
–H
2
O (MSH) endmember, with only substitution of Fe
2+
for Mg occurring in significant amounts. In experiments at 2 GPa, talc containing 0.48 apfu Fe
2+
begins to break down in the divariant field talc + anthophyllite + quartz at ~ 550 °C, a temperature ~ 270 °C lower than in the MSH system. At 4 GPa, Fe-bearing talc breaks down over a wide temperature interval in the divariant field talc + enstatite + coesite. The large decrease in temperature of the beginning of talc breakdown shows that Fe
2+
is partitioned strongly into enstatite and anthophyllite with respect to talc. In phase reversal experiments at 6.5 GPa, the beginning of the dehydration of 10-Å phase containing 0.48 apfu Fe
2+
was bracketed between 575 °C and 600 °C, a temperature ~ 100 °C lower than the MSH endmember reaction. The relative positions of the talc and 10-Å phase dehydration reactions indicate that the latter is able to accommodate greater Fe substitution, and is, therefore, more stable in Fe-bearing systems. In experiments at 6.2 GPa, 650 °C in the systems MgO–Al
2
O
3
–SiO
2
–H
2
O (MASH) and Na
2
O–MgO–Al
2
O
3
–SiO
2
–H
2
O (NMASH), 10-Å phase was synthesised that contains up to 0.5 apfu Al in the system MASH (compared to 0.8 in the starting material) and up to 0.4 apfu Al + 0.4 apfu Na in the system NMASH (compared to 0.7 of each of Al and Na in the starting material). Further experiments are required to determine if higher Al and Na contents in 10-Å phase are possible. The much higher Al and Na contents than found in talc indicate that, as with Fe, substitution of these elements enlarges the 10-Å phase stability field with respect to talc. In contrast to the effect of Fe, Al and Na also increase the stability of 10-Å phase relative to its thermal breakdown products enstatite + coesite.</description><identifier>ISSN: 0010-7999</identifier><identifier>EISSN: 1432-0967</identifier><identifier>DOI: 10.1007/s00410-019-1616-0</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aluminum oxide ; Bearing ; Breakdown ; Coesite ; Dehydration ; Earth and Environmental Science ; Earth Sciences ; Enstatite ; Experiments ; Geology ; Iron ; Magnesium oxide ; Mineral Resources ; Mineralogy ; Original Paper ; Petrology ; Phase stability ; Rheological properties ; Silica ; Silicon dioxide ; Solid solutions ; Subduction ; Subduction (geology) ; Subduction zones ; Substitution reactions ; Talc ; Temperature</subject><ispartof>Contributions to mineralogy and petrology, 2019-10, Vol.174 (10), p.1-13, Article 81</ispartof><rights>The Author(s) 2019</rights><rights>Contributions to Mineralogy and Petrology is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a2970-f27fbe5ef12e65bcacb91f5f3e8fe297780a8276c050b1b50378a13576b989a73</citedby><cites>FETCH-LOGICAL-a2970-f27fbe5ef12e65bcacb91f5f3e8fe297780a8276c050b1b50378a13576b989a73</cites><orcidid>0000-0002-3022-3235</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00410-019-1616-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00410-019-1616-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Howe, Harriet</creatorcontrib><creatorcontrib>Pawley, Alison R.</creatorcontrib><title>The effect of solid solution on the stability of talc and 10-Å phase</title><title>Contributions to mineralogy and petrology</title><addtitle>Contrib Mineral Petrol</addtitle><description>Talc and 10-Å phase are hydrous phases that are implicated in fluid processes and rheological behaviour in subduction zones. Natural samples of talc show limited compositional variation away from the MgO–SiO
2
–H
2
O (MSH) endmember, with only substitution of Fe
2+
for Mg occurring in significant amounts. In experiments at 2 GPa, talc containing 0.48 apfu Fe
2+
begins to break down in the divariant field talc + anthophyllite + quartz at ~ 550 °C, a temperature ~ 270 °C lower than in the MSH system. At 4 GPa, Fe-bearing talc breaks down over a wide temperature interval in the divariant field talc + enstatite + coesite. The large decrease in temperature of the beginning of talc breakdown shows that Fe
2+
is partitioned strongly into enstatite and anthophyllite with respect to talc. In phase reversal experiments at 6.5 GPa, the beginning of the dehydration of 10-Å phase containing 0.48 apfu Fe
2+
was bracketed between 575 °C and 600 °C, a temperature ~ 100 °C lower than the MSH endmember reaction. The relative positions of the talc and 10-Å phase dehydration reactions indicate that the latter is able to accommodate greater Fe substitution, and is, therefore, more stable in Fe-bearing systems. In experiments at 6.2 GPa, 650 °C in the systems MgO–Al
2
O
3
–SiO
2
–H
2
O (MASH) and Na
2
O–MgO–Al
2
O
3
–SiO
2
–H
2
O (NMASH), 10-Å phase was synthesised that contains up to 0.5 apfu Al in the system MASH (compared to 0.8 in the starting material) and up to 0.4 apfu Al + 0.4 apfu Na in the system NMASH (compared to 0.7 of each of Al and Na in the starting material). Further experiments are required to determine if higher Al and Na contents in 10-Å phase are possible. The much higher Al and Na contents than found in talc indicate that, as with Fe, substitution of these elements enlarges the 10-Å phase stability field with respect to talc. In contrast to the effect of Fe, Al and Na also increase the stability of 10-Å phase relative to its thermal breakdown products enstatite + coesite.</description><subject>Aluminum oxide</subject><subject>Bearing</subject><subject>Breakdown</subject><subject>Coesite</subject><subject>Dehydration</subject><subject>Earth and Environmental Science</subject><subject>Earth Sciences</subject><subject>Enstatite</subject><subject>Experiments</subject><subject>Geology</subject><subject>Iron</subject><subject>Magnesium oxide</subject><subject>Mineral Resources</subject><subject>Mineralogy</subject><subject>Original Paper</subject><subject>Petrology</subject><subject>Phase stability</subject><subject>Rheological properties</subject><subject>Silica</subject><subject>Silicon dioxide</subject><subject>Solid solutions</subject><subject>Subduction</subject><subject>Subduction (geology)</subject><subject>Subduction zones</subject><subject>Substitution reactions</subject><subject>Talc</subject><subject>Temperature</subject><issn>0010-7999</issn><issn>1432-0967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kM9KAzEQxoMoWKsP4C3gOTrJbv4dpVQrFLzUc0i2id2y7tYkPfQBfDJfzCwreBKGGYb5fd_Ah9AthXsKIB8SQE2BANWECioInKEZrStGQAt5jmYA5Sq11pfoKqU9lF1pPkPLzc5jH4JvMh4CTkPXbsd-zO3Q41K53FO2ru3afBqRbLsG236Li-H3Fz7sbPLX6CLYLvmb3zlHb0_LzWJF1q_PL4vHNbFMSyCByeA894EyL7hrbOM0DTxUXgVfCKnAKiZFAxwcdRwqqSytuBROK21lNUd3k-8hDp9Hn7LZD8fYl5eGMV0rKWrGCkUnqolDStEHc4jth40nQ8GMaZkpLVPSMmNaBoqGTZpU2P7dxz_n_0U_IDdrAA</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Howe, Harriet</creator><creator>Pawley, Alison R.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TN</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H96</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L.G</scope><scope>L6V</scope><scope>M2O</scope><scope>M2P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>R05</scope><orcidid>https://orcid.org/0000-0002-3022-3235</orcidid></search><sort><creationdate>20191001</creationdate><title>The effect of solid solution on the stability of talc and 10-Å phase</title><author>Howe, Harriet ; Pawley, Alison R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a2970-f27fbe5ef12e65bcacb91f5f3e8fe297780a8276c050b1b50378a13576b989a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aluminum oxide</topic><topic>Bearing</topic><topic>Breakdown</topic><topic>Coesite</topic><topic>Dehydration</topic><topic>Earth and Environmental Science</topic><topic>Earth Sciences</topic><topic>Enstatite</topic><topic>Experiments</topic><topic>Geology</topic><topic>Iron</topic><topic>Magnesium oxide</topic><topic>Mineral Resources</topic><topic>Mineralogy</topic><topic>Original Paper</topic><topic>Petrology</topic><topic>Phase stability</topic><topic>Rheological properties</topic><topic>Silica</topic><topic>Silicon dioxide</topic><topic>Solid solutions</topic><topic>Subduction</topic><topic>Subduction (geology)</topic><topic>Subduction zones</topic><topic>Substitution reactions</topic><topic>Talc</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Howe, Harriet</creatorcontrib><creatorcontrib>Pawley, Alison R.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oceanic Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Engineering Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><jtitle>Contributions to mineralogy and petrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Howe, Harriet</au><au>Pawley, Alison R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of solid solution on the stability of talc and 10-Å phase</atitle><jtitle>Contributions to mineralogy and petrology</jtitle><stitle>Contrib Mineral Petrol</stitle><date>2019-10-01</date><risdate>2019</risdate><volume>174</volume><issue>10</issue><spage>1</spage><epage>13</epage><pages>1-13</pages><artnum>81</artnum><issn>0010-7999</issn><eissn>1432-0967</eissn><abstract>Talc and 10-Å phase are hydrous phases that are implicated in fluid processes and rheological behaviour in subduction zones. Natural samples of talc show limited compositional variation away from the MgO–SiO
2
–H
2
O (MSH) endmember, with only substitution of Fe
2+
for Mg occurring in significant amounts. In experiments at 2 GPa, talc containing 0.48 apfu Fe
2+
begins to break down in the divariant field talc + anthophyllite + quartz at ~ 550 °C, a temperature ~ 270 °C lower than in the MSH system. At 4 GPa, Fe-bearing talc breaks down over a wide temperature interval in the divariant field talc + enstatite + coesite. The large decrease in temperature of the beginning of talc breakdown shows that Fe
2+
is partitioned strongly into enstatite and anthophyllite with respect to talc. In phase reversal experiments at 6.5 GPa, the beginning of the dehydration of 10-Å phase containing 0.48 apfu Fe
2+
was bracketed between 575 °C and 600 °C, a temperature ~ 100 °C lower than the MSH endmember reaction. The relative positions of the talc and 10-Å phase dehydration reactions indicate that the latter is able to accommodate greater Fe substitution, and is, therefore, more stable in Fe-bearing systems. In experiments at 6.2 GPa, 650 °C in the systems MgO–Al
2
O
3
–SiO
2
–H
2
O (MASH) and Na
2
O–MgO–Al
2
O
3
–SiO
2
–H
2
O (NMASH), 10-Å phase was synthesised that contains up to 0.5 apfu Al in the system MASH (compared to 0.8 in the starting material) and up to 0.4 apfu Al + 0.4 apfu Na in the system NMASH (compared to 0.7 of each of Al and Na in the starting material). Further experiments are required to determine if higher Al and Na contents in 10-Å phase are possible. The much higher Al and Na contents than found in talc indicate that, as with Fe, substitution of these elements enlarges the 10-Å phase stability field with respect to talc. In contrast to the effect of Fe, Al and Na also increase the stability of 10-Å phase relative to its thermal breakdown products enstatite + coesite.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00410-019-1616-0</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-3022-3235</orcidid><oa>free_for_read</oa></addata></record> |
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source | SpringerLink Journals - AutoHoldings |
subjects | Aluminum oxide Bearing Breakdown Coesite Dehydration Earth and Environmental Science Earth Sciences Enstatite Experiments Geology Iron Magnesium oxide Mineral Resources Mineralogy Original Paper Petrology Phase stability Rheological properties Silica Silicon dioxide Solid solutions Subduction Subduction (geology) Subduction zones Substitution reactions Talc Temperature |
title | The effect of solid solution on the stability of talc and 10-Å phase |
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