THERMOCHEMISTRY OF AG2S-CU2S SULFIDE SOLUTIONS - CONSTRAINTS DERIVED FROM COEXISTING SB2S3-BEARING AND AS2S3-BEARING SULFOSALTS

Authors
Citation
De. Harlov et Ro. Sack, THERMOCHEMISTRY OF AG2S-CU2S SULFIDE SOLUTIONS - CONSTRAINTS DERIVED FROM COEXISTING SB2S3-BEARING AND AS2S3-BEARING SULFOSALTS, Geochimica et cosmochimica acta, 59(21), 1995, pp. 4351-4365
Citations number
28
Categorie Soggetti
Geosciences, Interdisciplinary
ISSN journal
00167037
Volume
59
Issue
21
Year of publication
1995
Pages
4351 - 4365
Database
ISI
SICI code
0016-7037(1995)59:21<4351:TOASS->2.0.ZU;2-8
Abstract
We report experimental brackets (150-350 degrees C, evacuated silica t ubes) on (1) Ag-Cu partitioning between hexagonally close packed (hcp) -, face centered cubic (fcc)-, and body centered cubic (bcc)(Ag, Cu)(2 )S sulfides and the sulfosalts polybasite-pearceite [(Ag1-xCux)(16)(Sb , As)(2)S-11, 0.10 < x < 0.57] and high-skinnerite [(Cu-1-x, Ag-x)(3)S bS3, x < 0.26] and (2) Ag/Cu ratios of (Ag, Cu)(2)S sulfides coexistin g with polybasite and skinnerite, and polybasite and pyrargyrite [(Ag- 1-x, Cu-x)(3)SbS3, x < 0.21]. Based on these brackets on Ag-Cu partiti oning and activity-composition models for polybasite-pearceite and hig h-skinnerite (Harlov and Sack, 1994, 1995) we infer that (1) both hcp- and bcc-(Ag, Cu)(2)S sulfides exhibit positive deviations from ideali ty sufficient to produce metastable unmixing at slightly less than 90 degrees C and (2) fcc-(Ag, Cu)(2)S sulfides display more moderate posi tive deviations from ideal activity-composition relations, characteriz ed by a regular-solution-type parameter, W-Ag-Cu(fcc), = 5.4 +/- 0.2 k J/mol, for an assumed site multiplicity of Ag-Cu mixing of 2. The infe rred activity-composition relations for fcc- and bcc-(Ag, Cu)(2)S are consistent with brackets on the T - X(Cu) systematics of the transitio n between these phases (Skinner, 1966) and the calorimetric data of Gr onvold and Westrum (1986) for Ag2S provided that the effective site mu ltiplicity of Ag-Cu mixing in bcc-(Ag, Cu)(2)S decreases linearly from about 3 in Cu-poor to about 2 in Cu-rich compositions (X(Cu) similar to 0.315). Our constraints are also consistent with the calorimetric d ata for Cu2S (Gronvold and Westrum, 1987) and Skinner's (1966) bracket s on the T - X(Cu) systematics of the transition between fcc- and hcp- (Cu, Ag)(2)S provided that the effective site multiplicity of Ag-Cu mi xing in hcp-(Ag, Cu)(2)S approximates 3. From our brackets on Ag/Cu ra tios of (Ag, Cu)(2)S sulfides coexisting with polybasite and skinnerit e, and polybasite and pyrargyrite and calibrations for the Ag-Cu excha nge reactions we calculate average values of 5.30 +/- 1.14 and -31.1 /- 0.7 KJ/mol for the Gibbs energies of formation of hypothetical Cu16 Sb2S11 and Ag16Sb2S11 polybasite components from the simple sulfides o ver the temperature range 150-350 degrees C.