Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange

Beryllium is a significant constituent in sapphirine in some metamorphic and pegmatitic rocks, and thus could have a major effect on its stability relationships. Using the stoichiometries of reactions involving sapphirine and associated phases in the MgO-BeO-Al2O3-SiO2 (MBeAS) system in conjunction...

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Main Authors: Christy, Andrew, Grew, ES
Format: Article in Journal/Newspaper
Language:unknown
Published: Mineralogical Society of America
Subjects:
Online Access:http://hdl.handle.net/1885/86823
id ftanucanberra:oai:openresearch-repository.anu.edu.au:1885/86823
record_format openpolar
spelling ftanucanberra:oai:openresearch-repository.anu.edu.au:1885/86823 2024-01-14T09:59:36+01:00 Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange Christy, Andrew Grew, ES http://hdl.handle.net/1885/86823 unknown Mineralogical Society of America 0003-004X http://hdl.handle.net/1885/86823 American Mineralogist Keywords: beryllium crystal structure mineral synthesis P-T conditions sapphirine Journal article ftanucanberra 2023-12-15T09:34:25Z Beryllium is a significant constituent in sapphirine in some metamorphic and pegmatitic rocks, and thus could have a major effect on its stability relationships. Using the stoichiometries of reactions involving sapphirine and associated phases in the MgO-BeO-Al2O3-SiO2 (MBeAS) system in conjunction with molar volume data, we have plotted maps of the sapphirine solid-solution field in both μ-μ and μ-P space, where μ is the chemical potential of an exchange component such as (BeSi)(AlAl)-1. These maps give a pressure sequence of stable MBeAS univariant reactions and divariant assemblages that are consistent with experimental data, e.g., they show how Be stabilizes sapphirine + forsterite, which is rare in nature but readily synthesized over a wide P-T range in the presence of Be. We generate a MBeAS petrogenetic grid for sapphirine-bearing assemblages over the approximate range T = 700-900 °C, P = 0-2.5 GPa, identify divariant and univariant assemblages containing sapphirine with maximum Be, and determine the sense of variation of maximum Be content with P. At lower T, maximum Be occurs at the low-P limit of surinamite stability, ca. 0.5 GPa. At higher T, maximum Be increases with P, following the MBeAS univariant reactions involving (sapphirine + surinamite + orthopyroxene + chrysoberyl + forsterite or spinel). Natural assemblages containing sapphirine and its Be-rich near-analog khmaralite from the Napier Complex, Enderby Land, East Antarctica formed at higher T (900-1100 °C) than the experiments and in bulk compositions containing substantial Fe. Associated minerals include garnet, sillimanite, quartz, and magnesiotaaffeite-6N′3S ("musgravite"), whereas forsterite is absent and cordierite is a local, late phase. μ(BeSi)(AlAl)-1-μFeMg-1 diagrams show that the stability of magnesiotaaffeite-6N′3S causes the maximally beryllian khmaralite to shift from a magnesian composition in equilibrium with orthopyroxene + surinamite + forsterite + chrysoberyl, as in the MBeAS subsystem, to a more Fe-rich composition ... Article in Journal/Newspaper Antarc* Antarctica East Antarctica Enderby Land Australian National University: ANU Digital Collections East Antarctica Napier ENVELOPE(-58.440,-58.440,-62.167,-62.167)
institution Open Polar
collection Australian National University: ANU Digital Collections
op_collection_id ftanucanberra
language unknown
topic Keywords: beryllium
crystal structure
mineral synthesis
P-T conditions
sapphirine
spellingShingle Keywords: beryllium
crystal structure
mineral synthesis
P-T conditions
sapphirine
Christy, Andrew
Grew, ES
Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
topic_facet Keywords: beryllium
crystal structure
mineral synthesis
P-T conditions
sapphirine
description Beryllium is a significant constituent in sapphirine in some metamorphic and pegmatitic rocks, and thus could have a major effect on its stability relationships. Using the stoichiometries of reactions involving sapphirine and associated phases in the MgO-BeO-Al2O3-SiO2 (MBeAS) system in conjunction with molar volume data, we have plotted maps of the sapphirine solid-solution field in both μ-μ and μ-P space, where μ is the chemical potential of an exchange component such as (BeSi)(AlAl)-1. These maps give a pressure sequence of stable MBeAS univariant reactions and divariant assemblages that are consistent with experimental data, e.g., they show how Be stabilizes sapphirine + forsterite, which is rare in nature but readily synthesized over a wide P-T range in the presence of Be. We generate a MBeAS petrogenetic grid for sapphirine-bearing assemblages over the approximate range T = 700-900 °C, P = 0-2.5 GPa, identify divariant and univariant assemblages containing sapphirine with maximum Be, and determine the sense of variation of maximum Be content with P. At lower T, maximum Be occurs at the low-P limit of surinamite stability, ca. 0.5 GPa. At higher T, maximum Be increases with P, following the MBeAS univariant reactions involving (sapphirine + surinamite + orthopyroxene + chrysoberyl + forsterite or spinel). Natural assemblages containing sapphirine and its Be-rich near-analog khmaralite from the Napier Complex, Enderby Land, East Antarctica formed at higher T (900-1100 °C) than the experiments and in bulk compositions containing substantial Fe. Associated minerals include garnet, sillimanite, quartz, and magnesiotaaffeite-6N′3S ("musgravite"), whereas forsterite is absent and cordierite is a local, late phase. μ(BeSi)(AlAl)-1-μFeMg-1 diagrams show that the stability of magnesiotaaffeite-6N′3S causes the maximally beryllian khmaralite to shift from a magnesian composition in equilibrium with orthopyroxene + surinamite + forsterite + chrysoberyl, as in the MBeAS subsystem, to a more Fe-rich composition ...
format Article in Journal/Newspaper
author Christy, Andrew
Grew, ES
author_facet Christy, Andrew
Grew, ES
author_sort Christy, Andrew
title Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
title_short Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
title_full Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
title_fullStr Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
title_full_unstemmed Synthesis of beryllian sapphirine in the system MgO-BeO-Al 2 O 3 -SiO 2 -H 2 O and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: A chemographic study of Be content as a function of P , T , assemblage and FeMg -1 exchange
title_sort synthesis of beryllian sapphirine in the system mgo-beo-al 2 o 3 -sio 2 -h 2 o and comparison with naturally occurring beryllian sapphirine and khmaralite, part 2: a chemographic study of be content as a function of p , t , assemblage and femg -1 exchange
publisher Mineralogical Society of America
url http://hdl.handle.net/1885/86823
long_lat ENVELOPE(-58.440,-58.440,-62.167,-62.167)
geographic East Antarctica
Napier
geographic_facet East Antarctica
Napier
genre Antarc*
Antarctica
East Antarctica
Enderby Land
genre_facet Antarc*
Antarctica
East Antarctica
Enderby Land
op_source American Mineralogist
op_relation 0003-004X
http://hdl.handle.net/1885/86823
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