Chlorite is an ubiquitous hydrous phase in a variety of rock compositions involved in subduction processes when aluminum is a major chemical component. Because of its high H2O/Al2O3 ratio (close to 3/4), even small amounts of Al2O3 translates in large quantities of water potentially released at chlorite phase transformations. The chlorite stability field does not exceed 760-780 °C in a model NCFMASH peridotite, up to 4 GPa, but chlorite was found to extend to more than 850 °C at approx. 3 GPa in more complex chemical systems (Grove et al., 2006), in which the addition of Cr2O3 leads to Cr-chlorite with up to 1.4 wt.% Cr2O3. On the other hand, natural chlorite included in garnet porphyroblasts from ultra-high pressure ultramafic bodies may well exceed 2.3 wt.% Cr2O3. In order to discriminate whether Cr exerts such a profound effect on chlorite breakdown reactions, the thermodynamic properties as a function of different Cr content need to be explored. End-loaded piston cylinder synthesis experiments have been performed at 2.0 GPa, 800 °C in the model Cr2O3-MgO-Al2O3-SiO2-H2O system. Assuming that Cr is substituting for Al in the octahedral site of a clinochlore stoichiometry Mg10Al2(Si6Al2)O20(OH)16, three compositions JF1, JF2, and JF3 have been considered with Cr/(Cr+AlVI) = 0.15, 0.5 and 1.0 respectively. Gels were used as starting materials. In order to avoid the occurrence of metastable phases, as found in earlier experiments at the same PT conditions, 5 wt.% of natural clinochlore (Val Malenco, Italy) was added to the gels. Run products have been first identified by X-ray powder diffractometry, and analysed by EMPA. Cr-clinochlore has been successfully synthesized from JF1 seeded composition at 2.0 GPa, 800°C, 172 hrs. X-ray powder diffraction pattern suggests a single phase assemblage, with the basal peaks 001 and 002 at 6.2 and 12.4 degrees of 2 Theta respectively. Synthetic Cr chlorite has been analyzed by electron microprobe corroborating the X-ray powder diffraction observation. However, microprobe analysis revealed traces of orthopyroxene: however, coexisting orthopyroxenes contain no more than 0.02 Cr a.p.f.u. and Cr-clinochlore analyses are well within the expected composition (0.3 Cr a.p.f.u.). Crystal chemistry and cell parameters of synthetic Cr-clinoclore with different Cr contents will provide insights on the thermodynamic properties of chlorite and new constraints on phase equilibria in Cr bearing ultramafic systems.

The effects of Cr solubility in chlorites and its implications for Cr-clinochlore stability / J.K. Fischer, S. Poli, P. Fumagalli - In: 12th International Conference on Experimental Mineralogy, Petrology and Geochemistry September 7th - 10th 2008 / [a cura di] J. Konzett. - Innsbruck : Innsbruck University Press, 2008. - ISBN 9783902571663. - pp. 23-23 (( Intervento presentato al 12. convegno International Conference on Experimental Mineralogy, Petrology and Geochemistry (EMPG) tenutosi a Innsbruck nel 2008.

The effects of Cr solubility in chlorites and its implications for Cr-clinochlore stability

J.K. Fischer
Primo
;
S. Poli
Secondo
;
P. Fumagalli
Ultimo
2008

Abstract

Chlorite is an ubiquitous hydrous phase in a variety of rock compositions involved in subduction processes when aluminum is a major chemical component. Because of its high H2O/Al2O3 ratio (close to 3/4), even small amounts of Al2O3 translates in large quantities of water potentially released at chlorite phase transformations. The chlorite stability field does not exceed 760-780 °C in a model NCFMASH peridotite, up to 4 GPa, but chlorite was found to extend to more than 850 °C at approx. 3 GPa in more complex chemical systems (Grove et al., 2006), in which the addition of Cr2O3 leads to Cr-chlorite with up to 1.4 wt.% Cr2O3. On the other hand, natural chlorite included in garnet porphyroblasts from ultra-high pressure ultramafic bodies may well exceed 2.3 wt.% Cr2O3. In order to discriminate whether Cr exerts such a profound effect on chlorite breakdown reactions, the thermodynamic properties as a function of different Cr content need to be explored. End-loaded piston cylinder synthesis experiments have been performed at 2.0 GPa, 800 °C in the model Cr2O3-MgO-Al2O3-SiO2-H2O system. Assuming that Cr is substituting for Al in the octahedral site of a clinochlore stoichiometry Mg10Al2(Si6Al2)O20(OH)16, three compositions JF1, JF2, and JF3 have been considered with Cr/(Cr+AlVI) = 0.15, 0.5 and 1.0 respectively. Gels were used as starting materials. In order to avoid the occurrence of metastable phases, as found in earlier experiments at the same PT conditions, 5 wt.% of natural clinochlore (Val Malenco, Italy) was added to the gels. Run products have been first identified by X-ray powder diffractometry, and analysed by EMPA. Cr-clinochlore has been successfully synthesized from JF1 seeded composition at 2.0 GPa, 800°C, 172 hrs. X-ray powder diffraction pattern suggests a single phase assemblage, with the basal peaks 001 and 002 at 6.2 and 12.4 degrees of 2 Theta respectively. Synthetic Cr chlorite has been analyzed by electron microprobe corroborating the X-ray powder diffraction observation. However, microprobe analysis revealed traces of orthopyroxene: however, coexisting orthopyroxenes contain no more than 0.02 Cr a.p.f.u. and Cr-clinochlore analyses are well within the expected composition (0.3 Cr a.p.f.u.). Crystal chemistry and cell parameters of synthetic Cr-clinoclore with different Cr contents will provide insights on the thermodynamic properties of chlorite and new constraints on phase equilibria in Cr bearing ultramafic systems.
ultramafic system ; hydrous phase ; subduction ; chlorite ; Cr ; breakdown
Settore GEO/07 - Petrologia e Petrografia
2008
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/158228
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