EXPERIMENTAL DETERMINATION OF THE STABILITIES OF AU2S(CR) AT 25 °C AND AU(HS)2- AT 25-250 °C

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dc.contributor.author Tagirov B.R.
dc.contributor.author Schott J.
dc.contributor.author Baranova N.N.
dc.contributor.author Bannykh L.N.
dc.contributor.author Zotov A.V.
dc.date.accessioned 2024-07-20T12:14:05Z
dc.date.available 2024-07-20T12:14:05Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=13531831
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 14, 3689-3701
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/44515
dc.description.abstract The solubility of (i) Au(cr), (ii) mixtures of crystalline Ag2S-Ag3AuS2, and (iii) Ag3AuS2 (uytenbogaardtite)-AgAuS (petrovskaite) was measured at 25 °C, 1 bar, whereas the solubility of AgAuS(cr) was measured at 91-250 °C and Psat. These measurements were performed in aqueous sulphide solutions containing ~0.012-0.12 m of total reduced sulfur. At 25 °C sealed glass ampoules were employed, and Ti autoclaves allowing sampling of experimental solutions were used at higher temperatures. It was found that under investigated experimental conditions AgAuS dissolves incongruently with the formation of Ag3AuS2. The values of the following equilibrium reaction constants were determined:Au(cr) + H2 S0(aq) + HS- = Au (HS)2- + 0.5 H2(g) (i) K(i) = K(Au (HS)2-)Ag3 AuS2(cr) + HS- + 0.5 H2 S0(aq) = 1.5 Ag2 S(cr) + Au (HS)2- (ii) K(ii)1.5 AgAuS(cr) + HS- + 0.5 H2 S0(aq) = 0.5 Ag3 AuS2(cr) + Au (HS)2- (iii) K(iii) It was found that at 25 °C, 1 bar log K(i) = -5.62 ± 0.14, log K(ii) = -4.49 ± 0.26 and log K(iii) = -4.03 ± 0.15. Solubility data collected at higher temperatures resulted in the following values for log K(iii): -2.12 ± 0.25, -1.32 ± 0.12, and -1.04 ± 0.08 at 91, 150, and 250 °C, respectively (the latter value corresponds to the reaction 1.97 AgAuS(cr) + HS- + 0.5 H2 S0(aq) = 0.735Ag2.68 Au1.32 S2 (cr) + Au (HS)2- because Ag3AuS2(cr) undergoes a phase transition at 183 °C). These values are in good agreement with log K(iii) = -2.81 ± 0.10 obtained at 80 °C by Zotov et al. (Zotov, A.V., Baranova, N.N., Bannykh, L.N., 1996. Solubility of the gold sulfides Au2S and AgAuS in solutions containing hydrogen sulfide at 25-80 °C and pressures of 1 and 500 bar. Geochem. Int. 34, 216-221). The values of K(ii) and K(iii) determined in the present study were combined with the thermodynamic properties of Ag-Au sulphides reported by Osadchii and Rappo (Osadchii, E.G., Rappo, O.A., 2004. Determination of standard thermodynamic properties of sulfides in the Ag-Au-S system by means of a solid-state galvanic cell. Am. Miner. 89, 1405-1410), and thermodynamic properties for aqueous species and hydrogen from SUPCRT92 database to generate the values of K(Au (HS)2-). The results of the three experimental series performed at 25 °C, Psat (involving metallic gold (i) and Ag-Au sulphides (ii) and (iii)) yield the average value of log K(Au(HS)2-) = - 5.38 ± 0.25.Log K(Au(HS)2-) values derived at higher temperatures are -3.85 ± 0.20, -3.13 ± 0.29, -2.22 ± 0.20, and -1.96 ± 0.25 at 80, 91, 150 and 250 °C, respectively.At 150 and 250 °C these log K(Au(HS)2-) values are in close agreement with the data of Shenberger and Barnes (Shenberger, D.M., Barnes, H.L., 1989.Solubility of gold in aqueous solutions from 150 to 350 °C. Geochim.Cosmochim.Acta 53, 269-278).The log K(Au (HS)2-) value obtained at 25 °C, 1 bar combined with Au2S(cr) solubility products (Au2 S(cr) + 3 HS- + H+ = 2 Au (HS)2- and Au2 S(cr) + HS- + H+ = 2 AuH S0(aq)) measured at 25 °C by Renders and Seward (Renders, P.J., Seward, T.M., 1989.The stability of hydrosulphido- and sulphido-complexes of Au(I) and Ag(I) at 25 °C. Geochim.Cosmochim.Acta 53, 245-253) yields Δf G(298.15 K)° (Au2 S(cr)) = 19.41 ± 1.43 kJ / mol and log K(AuHS0) = -10.98 ± 0.30 for the reaction Au(cr) + H2 S0(aq) = AuH S0(aq) + 0.5 H2 (g) K(AuHS0) =. © 2006.
dc.title EXPERIMENTAL DETERMINATION OF THE STABILITIES OF AU2S(CR) AT 25 °C AND AU(HS)2- AT 25-250 °C
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2006.05.006


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