PHASE RELATIONS IN THE MGO-P2O5-H2O SYSTEM AND THE STABILITY OF PHOSPHOELLENBERGERITE: PETROLOGICAL IMPLICATIONS
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dc.contributor.author | Brunet F. | |
dc.contributor.author | Seifert F. | |
dc.contributor.author | Chopin C. | |
dc.date.accessioned | 2021-01-05T03:46:02Z | |
dc.date.available | 2021-01-05T03:46:02Z | |
dc.date.issued | 1998 | |
dc.identifier | https://elibrary.ru/item.asp?id=31800556 | |
dc.identifier.citation | Contributions to Mineralogy and Petrology, 1998, , 1, 54-70 | |
dc.identifier.issn | 0010-7999 | |
dc.identifier.uri | https://repository.geologyscience.ru/handle/123456789/22278 | |
dc.description.abstract | The polymorphic relations for Mg3(PO4)2 and Mg2PO4OH have been determined by reversed experiments in the temperature-pressure (T-P) range 500–1100°C, 2–30 kbar. The phase transition between the low-pressure phase farringtonite and Mg3(PO4)2-II, the Mg analogue of sarcopside, is very pressure dependent and was tightly bracketed between 625°C, 7 kbar and 850°C, 9 kbar. The high-temperature, high-pressure polymorph, Mg3(PO4)2-III, is stable above 1050°C at 10 kbar and above 900°C at 30 kbar. The low-pressure stability of farringtonite is in keeping with its occurrence in meteorites. The presence of iron stabilizes the sarcopside-type phase towards lower P. From the five Mg2PO4OH polymorphs only althausite, holtedahlite, β-Mg2PO4OH (the hydroxyl analogue of wagnerite) and ɛ-Mg2PO4OH were encountered. Relatively speaking, holtedahlite is the low-temperature phase (<600°C), ɛ-Mg2PO4OH the high-temperature, low-pressure phase and β-Mg2PO4OH the high-temperature, high-pressure phase, with an intervening stability field for althausite which extends from about 3 kbar at 500°C to about 12kbar at 800°C. Althausite and holtedahlite are to be expected in F-free natural systems under most geological conditions; however, wagnerite is the most common Mg-phosphate mineral, implying that fluorine has a major effect in stabilizing the wagnerite structure. Coexisting althausite and holtedahlite from Modum, S. Norway, show that minor fluorine is strongly partitioned into althausite (KD F/OH≈ 4) and that holtedahlite may incorporate up to 4 wt% SiO2. Synthetic phosphoellenbergerite has a composition close to (Mg0.9 0.1)2Mg12P8O38H8.4. It is a high-pressure phase, which breaks down to Mg2PO4OH + Mg3(PO4)2 + H2O below 8.5 kbar at 650°C, 22.5 kbar at 900°C and 30 kbar at 975°C. The stability field of the phosphate end-member of the ellenbergerite series extends therefore to much lower P and higher T than that of the silicate end-members (stable above 27 kbar and below ca. 725°C). Thus the Si/P ratio of intermediate members of the series has a great barometric potential, especially in the Si-buffering assemblage with clinochlore + talc + kyanite + rutile + H2O. Application to zoned ellenbergerite crystals included in the Dora-Maira pyrope megablasts, western Alps, reveals that growth zoning is preserved at T as high as 700–725°C. However, the record of attainment of the highest T and/or of decreasing P through P-rich rims (1 to 2 Si pfu) is only possible in the presence of an additional phosphate phase (OH-bearing or even OH-dominant wagnerite in these rocks), otherwise the trace amounts of P in the system remain sequestered in the core of Si-rich crystals (5 to 8 Si pfu) and can no longer react. | |
dc.title | PHASE RELATIONS IN THE MGO-P2O5-H2O SYSTEM AND THE STABILITY OF PHOSPHOELLENBERGERITE: PETROLOGICAL IMPLICATIONS | |
dc.type | Статья |
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