Abstract

Cinnabar (α-HgS) is the most common sulfide of mercury while metacinnabar (β-HgS), a high-temperature homogeneous polymorph of the mercury sulfide, is relatively rare, and the α phase of cinnabar transforms to the β phase at 344 °C. Meanwhile, there is a complete isomorphic series between HgS and HgSe, and the occurrence of Se-bearing metacinnabar is of great significance for the exploration of selenium resources. We studied through microscopic observation, electron-probe microanalysis, X-ray diffraction and field emission scanning electronic microscopy (FESEM) the Se-bearing metacinnabar of the Wanshan mercury ore field of southeastern Yangtze Block. These analyses, combined with physicochemical phase diagrams, constrained the textural and chemical evolution during the formation process of Se-bearing metacinnabar. Se-bearing metacinnabar was found in altered carbonatite, intergrown with cinnabar, sphalerite, pyrite, realgar and quartz. The Se-bearing metacinnabar contains 77.66–84.01 wt.% Hg, 0.18–1.17 wt.% Zn with extensive isomorphic substitution of Se and S (2.79–14.77 wt.% Se, 6.15–11.82 wt.% S). The presence of impurity elements (e.g., Zn and Se) is considered to be the key factor in expanding the stable range of Se-bearing metacinnabar. The cinnabar generated by the transformation of Se-bearing metacinnabar is characterized by inclusions of Hg-bearing sphalerite and pores, which indicate that this process was carried out through a coupled dissolution–reprecipitation (CDR) reaction. The formation temperature of Se-bearing metacinnabar is higher than that of cinnabar, and according to the phase relations between sulfides and selenides, we propose that logfS2(g) of ore-forming fluids is constrained within −15.663 to −13.141, and logfSe2 < logfS2–3.994 (150 °C).

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