Iron and Sulfur Isotope Factors of Pyrite: Data from Experimental Mössbauer Spectroscopy and Heat Capacity


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Abstract

Mössbauer spectra of pyrite (FeS2) are measured within a temperature range of 90–295 K. The isomer shift is described by the Debye model with a Mössbauer temperature θM = 551.4 K. These results are used to calculate the kinetic energy of thermal vibrations of the iron sublattice of pyrite and the iron β-factor for pyrite: 103\({\text{ln}}{{\beta }_{{^{{{\text{57}}}}{\text{Fe}}{{{\text{/}}}^{{{\text{54}}}}}{\text{Fe}}}}}\) = (1.2665 ± 0.0391)x – (0.4584 ± 0.0283) × 10–2x2 + (0.2581 ± 0.0239) × 10–4x3; x = 106/T 2 (K–2). The calculated iron β-factor in pyrite is in good agreement with results of ab initio calculations, 57Fe nuclear inelastic X-ray resonant scattering in synchrotron experiments, and direct isotope exchange experiments between pyrite and Fe2+ dissolved in water. The heat capacity of pyrite is measured within a temperature range of 79–300 K and is described using the Thirring expansion. Based on this expansion, the kinetic energy of thermal vibrations of the total crystalline lattice of pyrite is calculated. The kinetic energy of the thermal vibrations of the sulfur sublattice in pyrite is found by subtracting the kinetic energy of the iron sublattice from the total kinetic energy of pyrite crystalline lattice. The temperature dependence of 34S/32S β-factor for pyrite, which was calculated from the kinetic energy of the sulfur sublattice, is 103\({\text{ln}}{{\beta }_{{^{{{\text{34}}}}{\text{Fe}}{{{\text{/}}}^{{{\text{32}}}}}{\text{Fe}}}}}\) = (1.7532 ± 0.0623) x – (1.0470 ± 0.0752) × 10–2x2 + (1.0424 ± 0.1126) × 10–4x3; x = 106/T2 (K–2). This value of the 34S/32S β-factor is in good agreement with the ab initio calculations and with results of isotope-exchange experiments in the pyrite–sphalerite–galena system.

About the authors

V. B. Polyakov

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences

Author for correspondence.
Email: polyakov@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432

E. G. Osadchii

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences

Author for correspondence.
Email: euo@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432

M. V. Voronin

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432

V. O. Osadchii

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432

L. V. Sipavina

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432

D. A. Chareev

Korzhinckii Institute of Experimental Mineralogy (IEM), Russian Academy of Sciences; Eltsin Ural Federal University; Kazan Federal University

Email: euo@iem.ac.ru
Russian Federation, Chernogolovka, Moscow oblast, 142432; Yekaterinburg, 620002; Kazan, 420008

A. V. Tyurin

Kurnakov Institute of General and Inorganic Chemistry (IONKh), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Moscow, 119991

V. M. Gurevich

Kurnakov Institute of General and Inorganic Chemistry (IONKh), Russian Academy of Sciences; Vernadsky Institute of Geochemistry and Analytical Chemistry (GEOKhI), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Moscow, 119991; Moscow, 119991

K. S. Gavrichev

Kurnakov Institute of General and Inorganic Chemistry (IONKh), Russian Academy of Sciences

Email: euo@iem.ac.ru
Russian Federation, Moscow, 119991

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