Substitution mechanisms in In-, Au-, and Cu-bearing sphalerites studied by X-ray absorption spectroscopy of synthetic compounds and natural minerals

被引:27
作者
Filimonoya, Olga N. [1 ]
Trigub, Alexander L. [1 ,2 ]
Tonkacheev, Dmitriy E. [1 ]
Nickolsky, Max S. [1 ,8 ]
Kvashnina, Kristina O. [3 ,7 ]
Chareev, Dmitriy A. [4 ,5 ,6 ]
Chaplygin, Ilya, V [1 ]
Kovalchuk, Elena, V [1 ]
Lafuerza, Sara [3 ]
Tagirov, Boris R. [1 ]
机构
[1] RAS, Inst Geol Ore Deposits IGEM, 35 Staromonetnyi Per, Moscow 119017, Russia
[2] Natl Res Ctr Kurchatov Inst, 1 Akad Kurchatova Pl, Moscow 123182, Russia
[3] ESRF, 71 Ave Martyrs,CS40220, F-38043 Grenoble 9, France
[4] IEM RAS, Chernogoiovka 142432, Moscow Region, Russia
[5] Ural Fed Univ, Inst Phys & Technol, Mira St 19, Ekaterinburg 620002, Russia
[6] Kazan Fed Univ, Inst Geol & Petr Technol, Kremlyovskaya 4-5, Kazan 420008, Russia
[7] HZDR, Inst Resource Ecol, POB 510119, D-01314 Dresden, Germany
[8] Russian Acad Sci, Frumkin Inst Phys Chem & Electrochem, Leninskii Pr 31,Korp 4, Moscow 119071, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
Indium; gold; copper; cadmium; trace elements; sphalerite; synthetic minerals; X-ray absorption spectroscopy; EXAFS; OXIDATION-STATE; CHEMICAL-STATE; INVISIBLE GOLD; FE; SULFIDES; CENTERS; PROGRAM; RADII; EXAFS; GE;
D O I
10.1180/mgm.2019.10
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
Sphalerite is the main source of In - a 'critical' metal widely used in high-tech electronics. In this mineral the concentration of In is commonly correlated directly with Cu content. Here we use X-ray absorption spectroscopy of synthetic compounds and natural crystals in order to investigate the substitution mechanisms in sphalerites where In is present, together with the group 11 metals. All the admixtures (Au, Cu, In) are distributed homogeneously within the sphalerite matrix, but their structural and chemical states are different. In all the samples investigated In3+ replaces Zn in the structure of sphalerite. The In ligand distance increases by 0.12 A and 0.09-0.10 A for the 1st and 2nd coordination shells, respectively, in comparison with pure sphalerite. The In-S distance in the 3rd coordination shell is close to the one of pure sphalerite. Gold in synthetic sphalerites is coordinated with sulfur (N-S = 2.4-2.5, RA(u-S) = 2.35 +/- 0.01 angstrom). Our data suggest that at high Au concentrations (0.03-0.5 wt.%) the Au2S clusters predominate, with a small admixture of the Au+ solid solution with an Au-S distance of 2.5 angstrom. Therefore, the homogeneous character of a trace-element distribution, which is commonly observed in natural sulfides, does not confirm formation of a solid solution. In contrast to Au, the presence of Cu+ with In exists only in the solid-solution state, where it is tetrahedrally coordinated with S atoms at a distance of 2.30 +/- 0.03 angstrom. The distant coordination shells of Cu are disordered. These results demonstrate that the group 11 metals (Cu, Ag and Au) can exist in sphalerite in the metastable solid-solution state. The solid solution forms at high temperature via the charge compensation scheme 2Zn(2+)<-> Me++Me3+. The final state of the trace elements at ambient temperature is governed by the difference in ionic radii with the main component (Zn), and concentration of admixtures.
引用
收藏
页码:435 / 451
页数:17
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