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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Veröffentlicht in:Contributions to mineralogy and petrology 2019-10, Vol.174 (10), p.1-13, Article 81
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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.
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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. 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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. 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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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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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