The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c

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Standard

The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c. / Karup-Møller, Sven; Makovicky, Emil; Barnes, Sarah-Jane.

In: Mineralogical Magazine, Vol. 72, No. 4, 2008, p. 941-851.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Karup-Møller, S, Makovicky, E & Barnes, S-J 2008, 'The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c', Mineralogical Magazine, vol. 72, no. 4, pp. 941-851.

APA

Karup-Møller, S., Makovicky, E., & Barnes, S-J. (2008). The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c. Mineralogical Magazine, 72(4), 941-851.

Vancouver

Karup-Møller S, Makovicky E, Barnes S-J. The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c. Mineralogical Magazine. 2008;72(4):941-851.

Author

Karup-Møller, Sven ; Makovicky, Emil ; Barnes, Sarah-Jane. / The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c. In: Mineralogical Magazine. 2008 ; Vol. 72, No. 4. pp. 941-851.

Bibtex

@article{15154030c13311dd8ca2000ea68e967b,
title = "The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c",
abstract = "The sulphur-poor portions of the dry condensed Cu-Fe-Pd-S system were studied at 1000°C, 900°C and 725°C by synthesis in evacuated silicate glass tubes, along with textural observations and electron microprobe analyses of equilibrated reaction products. Sulphide melt coexists with Cu-Fe-Pd alloys, bornite, Fe1-xS and iss (intermediate solid solution, Cabri, 1973) and Pd4S. Compositional data were obtained for the associations bornite-alloy-melt, pyrrhotite-alloy-melt and for immiscible Cu-rich sulphide melts. Partition coefficients for all three metals were derived for the association alloy-melt. Formation of the two new Cu-Pd alloy minerals, skaergaardite and nielsenite, is discussed in terms of the present findings. ",
author = "Sven Karup-M{\o}ller and Emil Makovicky and Sarah-Jane Barnes",
year = "2008",
language = "English",
volume = "72",
pages = "941--851",
journal = "Mineralogical Magazine",
issn = "0026-461X",
publisher = "Mineralogical Society",
number = "4",

}

RIS

TY - JOUR

T1 - The metal-rich portions of the phase system Cu-Fe-Pd-S at 100°c, 900°c and 725°c

AU - Karup-Møller, Sven

AU - Makovicky, Emil

AU - Barnes, Sarah-Jane

PY - 2008

Y1 - 2008

N2 - The sulphur-poor portions of the dry condensed Cu-Fe-Pd-S system were studied at 1000°C, 900°C and 725°C by synthesis in evacuated silicate glass tubes, along with textural observations and electron microprobe analyses of equilibrated reaction products. Sulphide melt coexists with Cu-Fe-Pd alloys, bornite, Fe1-xS and iss (intermediate solid solution, Cabri, 1973) and Pd4S. Compositional data were obtained for the associations bornite-alloy-melt, pyrrhotite-alloy-melt and for immiscible Cu-rich sulphide melts. Partition coefficients for all three metals were derived for the association alloy-melt. Formation of the two new Cu-Pd alloy minerals, skaergaardite and nielsenite, is discussed in terms of the present findings.

AB - The sulphur-poor portions of the dry condensed Cu-Fe-Pd-S system were studied at 1000°C, 900°C and 725°C by synthesis in evacuated silicate glass tubes, along with textural observations and electron microprobe analyses of equilibrated reaction products. Sulphide melt coexists with Cu-Fe-Pd alloys, bornite, Fe1-xS and iss (intermediate solid solution, Cabri, 1973) and Pd4S. Compositional data were obtained for the associations bornite-alloy-melt, pyrrhotite-alloy-melt and for immiscible Cu-rich sulphide melts. Partition coefficients for all three metals were derived for the association alloy-melt. Formation of the two new Cu-Pd alloy minerals, skaergaardite and nielsenite, is discussed in terms of the present findings.

M3 - Journal article

VL - 72

SP - 941

EP - 851

JO - Mineralogical Magazine

JF - Mineralogical Magazine

SN - 0026-461X

IS - 4

ER -

ID: 8832485