Magnetic properties and cation ordering in two synthetic bornite samples, Cu<sub>5</sub>(Fe, Mn)S<sub>4</sub>

Authors

  • Miria Borgheresi
  • Francesco Di Benedetto
  • Andrea Caneschi
  • Maurizio Romanelli
  • David J. Vaughan

DOI:

https://doi.org/10.2451/2011PM0009

Keywords:

bornite, intervalence charge transfer, EPR spectroscopy, SQUID magnetometry, EPMA, Mn(II)

Abstract

Periodico di Mineralogia (2011), 80, 1 (Special Issue), 113-121 - DOI: 10.2451/2011PM0009
Special Issue in memory of Sergio Lucchesi


Magnetic properties and cation ordering in two synthetic bornite samples, Cu5(Fe, Mn)S4

Miria Borgheresi1, Francesco Di Benedetto2,*, Andrea Caneschi2, Maurizio Romanelli2 and David J.Vaughan3

1Via Matteotti 27, Pontassieve, Firenze, Italy
2Dipartimento di Chimica, Università di Firenze, Sesto Fiorentino, Firenze, Italy
3Williamson Research Centre for Molecular Environmental Science, and School of Earth, Atmospheric and Environmental Sciences, University of Manchester, UK
*Corresponding author: francesco.dibenedetto@unifi.it

Abstract

The magnetic properties of a synthetic bornite, Cu5FeS4, and of a Mn-bearing synthetic bornite were investigated using Superconducting Quantum Interference Device (SQUID) magnetometry and room temperature X-band Electron Paramagnetic Resonance (EPR) spectroscopy. Samples were synthesised from the elements using conventional dry methods. Chemical and phase compositions of the samples were confirmed by means of Electron Probe Micro-Analysis (EPMA) and by powder X-Ray Diffraction (XRD).
Experimental results, interpreted using spectral simulations, highlight the superexchange nature of ionic interactions between paramagnetic centres and the role played by partial intervalence charge transfer between the  Fe(III) and Cu(I) species in natural and synthetic bornite. The cation distribution in synthetic samples was shown to be different from the natural sample, in spite of the close similarity in chemical composition and structure.


Key words: bornite; intervalence charge transfer; EPR spectroscopy; SQUID magnetometry; EPMA; Mn(II).

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