scispace - formally typeset
Journal ArticleDOI

Instability of sapphirine at high pressures

Reads0
Chats0
TLDR
The stability field of Mg-sapphirines is limited at high pressures through the solid-solid breakdown reaction sapphirine⇌pyrope = corundum+spinel, the univariant curve originating from an invariant point located at 22 kb, 880°C to 30 kb, 1350°C as discussed by the authors.
Abstract
The stability field of Mg-sapphirines is limited at high pressures through the solid-solid breakdown reaction sapphirine⇌pyrope = corundum+spinel, the univariant curve originating from an invariant point located at 22 kb, 880°C to 30 kb, 1350°C. Under water pressures less than 22 kb sapphirines exhibit the same low-temperature breakdown into the assemblage chlorite+corundum+spinel as determined by Seifert (1974) between 1 kb and 7 kb thus resulting in one continuous univariant lower stability limit extending from 1 kb, about 650°C through 10 kb, 770°C to the invariant point at 22 kb, 880°C. If $$P_{{\text{H}}_{\text{2}} {\text{0}}} < P_{{\text{total}}} $$ , the stability field of sapphirine will expand towards lower temperatures. The occurrence of sapphirine in mantle depths requires rather aluminous bulk compositions, high geothermal gradients and/or $$P_{{\text{H}}_{\text{2}} {\text{0}}} < P_{{\text{total}}} $$ , with total pressures not exceeding 30 kb. Thus sapphirine is probably not a stable phase in the lower portions of lithospheric plates and the underlying asthenosphere.

read more

Citations
More filters
Journal ArticleDOI

An internally consistent thermodynamic data set for phases of petrological interest

TL;DR: In this paper, the thermodynamic properties of 154 mineral endmembers, 13 silicate liquid end-members and 22 aqueous fluid species are presented in a revised and updated data set.
Journal ArticleDOI

An improved and extended internally consistent thermodynamic dataset for phases of petrological interest, involving a new equation of state for solids

TL;DR: In this paper, the Tait equation of state (TEOS) was used to model the temperature dependence of both the thermal expansion and bulk modulus in a consistent way, which has led to improved fitting of the phase equilibrium experiments.
Journal ArticleDOI

An enlarged and updated internally consistent thermodynamic dataset with uncertainties and correlations: the system K2O–Na2O–CaO–MgO–MnO–FeO–Fe2O3–Al2O3–TiO2–SiO2–C–H2–O2

TL;DR: In this paper, a revised and much enlarged version of the thermodynamic dataset given earlier (Holland & Powell, 1985) is presented, which includes data for 123 mineral and fluid end-members made consistent with over 200 P-T-XCO2-fO2 phase equilibrium experiments.
Journal ArticleDOI

On ultrahigh-temperature crustal metamorphism

TL;DR: In this article, a review of UHT metamorphism is presented, including the history of experiments that have ultimately lead to the precise P-T constraints we can now place on the generation and evolution of UHP mineral assemblages.
Journal ArticleDOI

On ultrahigh temperature crustal metamorphism: phase equilibria, trace element thermometry, bulk composition, heat sources, timescales and tectonic settings

TL;DR: In this article, a ferric iron activity-composition thermodynamic model for sapphirine was developed, allowing phase diagram calculations for oxidised rock compositions and quantification of UHT conditions via trace element thermometry, with Zr-inrutile more commonly recording higher temperatures than Ti-inzircon.
References
More filters
Journal ArticleDOI

Apparatus for phase‐equilibrium measurements at pressures up to 50 kilobars and temperatures up to 1750°C

TL;DR: In this paper, the construction and calibration of apparatus utilizing a solid pressure medium for phase-equilibrium studies at elevated temperatures and pressures are described, and a new determination of the thallium transition, 37.1±1.3 kilobars, is given.
Journal ArticleDOI

An interlaboratory comparison of piston-cylinder pressure calibration using the albite-breakdown reaction.

TL;DR: In this article, an attempt is made to compare pressure calibration methods among several laboratories in an unbiased way to produce some indication of the bandwidth of observations on the pressure of an equilibrium reaction where sources of discrepancy not resulting from pressure calibration are likely to have been eliminated.
Related Papers (5)