An experimental study of the stability of copper chloride complexes in water vapor at elevated temperatures and pressures

被引:111
作者
Archibald, SM [1 ]
Migdisov, AA [1 ]
Williams-Jones, AE [1 ]
机构
[1] McGill Univ, Dept Earth & Planetary Sci, Montreal, PQ H3A 2A7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/S0016-7037(01)00867-5
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The solubility of copper chloride in liquid-undersaturated HCl-bearing water vapor was investigated experimentally at temperatures of 280 to 320degreesC and pressures up to 103 bars. Results of these experiments show that the solubility of copper in the vapor phase is significant and increases with increasing fH(2)O but is retrograde with respect to temperature. This solubility is attributed to the formation of hydrated copper-chloride gas species, interpreted to have a copper-chlorine ratio of 1:1 (e.g.. CuCl, Cu,Cl,, etc.) and a hydration number varying from 7.6 at 320degreesC, to 6.0 at 300degreesC, and 6.1 at 280degreesC. Complex formation is proposed to have occurred through the reaction: 3 CuClsolid + nH(2)O(gas) reversible arrow Cu3Cl3.(H2O)(n)(gas) (A1) Log K values determined for this reaction are -21.46 +/- 0.05 at 280degreesC (n = 7.6), -19.03 +/- 0.10 at 300degreesC (n = 6.0), and -19.45 +/- 0.12 at 320degreesC (n = 6.1) if it is assumed that the vapor species is the trimer, Cu3Cl3(H2O)(6-8). Calculations based on the above data indicate that at 300degreesC and HCl fluxes encountered in passively degassing volcanic systems, the vapor phase could transport copper in concentrations as high as 280 ppm. Theoretically, this vapor could form an economic copper deposit (e.g., 50 million tonnes of 0.5% Cu) in as little as similar to20,500 yr. Copyright (C) 2002 Elsevier Science Ltd.
引用
收藏
页码:1611 / 1619
页数:9
相关论文
共 57 条
[1]   The stability of Au-chloride complexes in water vapor at elevated temperatures and pressures [J].
Archibald, SM ;
Migdisov, AA ;
Williams-Jones, AE .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (23) :4413-4423
[2]   SOLUBILITY OF SODIUM-CHLORIDE AND SULFATE IN SUBCRITICAL AND SUPERCRITICAL WATER-VAPOR FROM 450-550-DEGREES-C AND 100-250 BAR [J].
ARMELLINI, FJ ;
TESTER, JW .
FLUID PHASE EQUILIBRIA, 1993, 84 :123-142
[3]  
Barnes H., 1997, Geochemistry of Hydrothermal Ore Deposits, V3rd, P699
[4]   THE SYSTEM NACL-H2O - RELATIONS OF VAPOR-LIQUID NEAR THE CRITICAL-TEMPERATURE OF WATER AND OF VAPOR-LIQUID-HALITE FROM 300-DEGREES-C TO 500-DEGREES-C [J].
BISCHOFF, JL ;
ROSENBAUER, RJ ;
PITZER, KS .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1986, 50 (07) :1437-1444
[5]   THE THERMODYNAMICS OF GASEOUS CUPROUS CHLORIDE, MONOMER AND TRIMER [J].
BREWER, L ;
LOFGREN, NL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1950, 72 (07) :3038-3045
[6]   Complexation of metal ions in brines:: application of electronic spectroscopy in the study of the Cu(II)-LiCl-H2O system between 25 and 90°C [J].
Brugger, J ;
McPhail, DC ;
Black, J ;
Spiccia, L .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (16) :2691-2708
[7]   HEAVY-METAL CHEMISTRY OF ATMOSPHERIC PARTICULATE MATTER EMITTED BY MOUNT ETNA VOLCANO [J].
BUATMENARD, P ;
ARNOLD, M .
GEOPHYSICAL RESEARCH LETTERS, 1978, 5 (04) :245-248
[8]  
BURNHAM WC, 1997, GEOCHEMISTRY HYDROTH, P63
[10]   A MASS-TRANSFER MODEL FOR COPPER AND MOLYBDENUM IN MAGMATIC HYDROTHERMAL SYSTEMS - THE ORIGIN OF PORPHYRY-TYPE ORE-DEPOSITS [J].
CANDELA, PA ;
HOLLAND, HD .
ECONOMIC GEOLOGY, 1986, 81 (01) :1-19