4.7 Article

Partitioning of Cu between mafic minerals, Fe-Ti oxides and intermediate to felsic melts

Journal

GEOCHIMICA ET COSMOCHIMICA ACTA
Volume 151, Issue -, Pages 86-102

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2014.12.010

Keywords

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Funding

  1. NBRP of China [2014CB440802]
  2. NSF of China [41373061, 41121002, 41173070]
  3. GIGCAS [Y234152001, SKLIG-JY-14-01]
  4. Bayerisches Geoinstitut

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This study used improved capsule technique i.e., Pt95Cu05 or Au95Cu05 alloy capsules as Cu sources to determine Cu partitioning between mafic minerals, Fe-Ti oxides and intermediate to felsic melts at 0.5-2.5 GPa, 950-1100 degrees C and various oxygen fugacities (fO(2)). In combination with the data from the mafic composition systems, the results demonstrate that Cu is generally highly incompatible in mafic minerals and moderately incompatible to compatible in Fe-Ti oxides. The general order of mineral/melt Cu partition coefficients (D-Cu) is garnet (0.01-0.06) <= olivine (0.04-0.20) approximate to opx (0.04-0.24) approximate to amphibole (0.04-0.20) <= cpx (0.04-0.45) <= magnetite, titanomagnetite and Cr-spinel (0.18-1.83). The variations in D-Cu depend mainly on temperature, fO(2) or mineral composition. In general, D-Cu for olivine (and perhaps opx) increases with decreasing temperature and increasing fO(2). D-Cu increases for cpx with Na+ (pfu) in cpx, for magnetite and Cr-spinel with Fe3+ (pfu) in these phases and for titanomagnetite with Ti4+ (pfu) in this phase. The large number of D-Cu data (99 pairs) serves as a foundation for quantitatively understanding the behavior of Cu during magmatic processes. The generation of intermediate to felsic magmas via fractional crystallization or partial melting of mafic rocks (magmas) at deep levels of crust involves removal of or leaving assemblages of mafic minerals + Fe-Ti oxides +/- sulfides. With our D-Cu data on mafic minerals and Fe-Ti oxides, D-Cu(bulk) values around 0.2 were obtained for the sulfide-free assemblages. Cu will thus be concentrated efficiently in the derived melts during these two processes if sulfides are absent or negligible, explaining that high fO(2) and sulfide-destabilization are favorable to formation of the porphyry Cu system. (C) 2014 Elsevier Ltd. All rights reserved.

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