An XAS study of the structure and thermodynamics of Cu(I) chloride complexes in brines up to high temperature (400 °C, 600 bar)

被引:128
作者
Brugger, J. [1 ]
Etschmann, B.
Liu, W.
Testemale, D.
Hazemann, J. L.
Emerich, H.
van Beek, W.
Proux, O.
机构
[1] Univ Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5000, Australia
[2] S Australian Museum, Div Mineral, Adelaide, SA 5000, Australia
[3] Monash Univ, Sch Geosci, CSIRO Explorat & Min, Clayton, Vic 3168, Australia
[4] European Synchrotron Radiat Facil, SNBL, F-38043 Grenoble, France
[5] Inst Neel, Dept MCMF, CNRS, F-38042 Grenoble, France
[6] European Synchrotron Radiat Facil, FAME, F-38043 Grenoble, France
[7] LGIT, CNRS, F-38041 Grenoble 9, France
基金
澳大利亚研究理事会;
关键词
D O I
10.1016/j.gca.2007.08.003
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 [地球物理学]; 070902 [地球化学];
摘要
The transport and deposition of copper in saline hydrothermal fluids are controlled by the stability of copper(I) complexes with ligands such as chloride. Despite their role in the formation of most hydrothermal copper deposits, the nature and stability of Cu(I) chloride complexes in highly saline brines remains controversial. We present new X-ray absorption data (P = 600 bar, T = 25-400 degrees C, salinity up to 17.2 m CI), which indicate that the linear CuClx1-x (x = 1, 2) complexes are stable up to supercritical conditions. Distorted trigonal planar CuCl32- complexes predominate at room temperature and at high salinity (>3 m LiCl): subtle changes in the XANES spectrum with increasing salinity may reflect geometric distortions of this CuCl32- complex. Similar changes were observed in UV-Vis data [Liu, W., Brugger, J., McPhail, D.C., Spiccia, L., 2002. A spectrophotometric study of aqueous copper(I) chloride complexes in LiCl solutions between 100 degrees C and 250 degrees C. Geochim. Cosmochim. Acta 66, 3615-3633], and were erroneously interpreted as a new species, CuCl42-. Our XAS data and ab-initio XANES calculations show that this tetrahedral species is not present to any significant degree in our solutions. The stability of the CuCl32- complexe decreases with increasing temperature; under supercritical conditions and in brines under magmatic-hydro thermal conditions (e.g., 15.58 m Cl, 400 degrees C, 600 bar), only the linear Cu(I) chloride complexes were observed. This result and the instability of the CuCl42- complex are also consistent with the recent ab-initio molecular dynamic calculations of Sherman [Sherman D. M. (2007) Complexation of Cu+ in hydrothermal NaCl brines: ab-initio molecular dynamics and energetics. Geochim. Cosmochim. Acta 71, 714-722]. This study illustrates the power of the quantitative nature of XANES and EXAFS measurements for deciphering the speciation of weak transition metal complexes up to magmatic-hydrothermal conditions. The systematic XANES data are used to retrieve the formation constant for CuCl32- at 150 degrees C, which is in good agreement with the reinterpretation of the UV-Vis data of Liu et al. (Liu et al., 2002). At high temperatures (>> 400 degrees C), the solubility of chalcopyrite in equilibrium with hematite-magnetite-pyrite and K-feldspar muscovite-quartz calculated with the new properties is lower than that calculated using the previous model, and the calculated solubilities are at the lower end of the range of values measured in brine inclusions from porphyry copper systems. (C) 2007 Elsevier Ltd. All rights reserved.
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收藏
页码:4920 / 4941
页数:22
相关论文
共 79 条
[1]
STABILITY OF METAL HALIDE COMPLEXES IN AQUEOUS SOLUTION .7. CHLORIDE COMPLEXES OF COPPER(I) [J].
AHRLAND, S ;
RAWSTHORNZ, J .
ACTA CHEMICA SCANDINAVICA, 1970, 24 (01) :157-+
[2]
Real-space multiple-scattering calculation and interpretation of x-ray-absorption near-edge structure [J].
Ankudinov, AL ;
Ravel, B ;
Rehr, JJ ;
Conradson, SD .
PHYSICAL REVIEW B, 1998, 58 (12) :7565-7576
[3]
Theoretical analysis of x-ray absorption near-edge structure of transition-metal aqueous complexes in solution at the metal K edge [J].
Benfatto, M ;
Solera, JA ;
Chaboy, J ;
Proietti, MG ;
Garcia, J .
PHYSICAL REVIEW B, 1997, 56 (05) :2447-2452
[4]
Evidence of distorted fivefold coordination of the Cu2+ aqua ion from an x-ray-absorption spectroscopy quantitative analysis -: art. no. 174205 [J].
Benfatto, M ;
D'Angelo, P ;
Della Longa, S ;
Pavel, NV .
PHYSICAL REVIEW B, 2002, 65 (17) :1742051-1742055
[5]
The MXAN procedure:: a new method for analysing the XANES spectra of metalloproteins to obtain structural quantitative information [J].
Benfatto, M ;
Della Longa, S ;
Natoli, CR .
JOURNAL OF SYNCHROTRON RADIATION, 2003, 10 :51-57
[6]
Geometrical fitting of experimental XANES spectra by a full multiple-scattering procedure [J].
Benfatto, M ;
Della Longa, S .
JOURNAL OF SYNCHROTRON RADIATION, 2001, 8 (04) :1087-1094
[7]
Density functional calculation of the electronic absorption spectrum of Cu+ and Ag+ aqua ions [J].
Bernasconi, L ;
Blumberger, J ;
Sprik, M ;
Vuilleumier, R .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (23) :11885-11899
[8]
A XANES study of Cu speciation in high-temperature brines using synthetic fluid inclusions [J].
Berry, Andrew J. ;
Hack, Alistair C. ;
Mavrogenes, John A. ;
Newville, Matthew ;
Sutton, Stephen R. .
AMERICAN MINERALOGIST, 2006, 91 (11-12) :1773-1782
[9]
Bethke C.M., 1996, Geochemical Reaction Modeling: Concepts and Applications
[10]
THEORY AND APPLICATIONS OF CHARGE-TRANSFER-TO-SOLVENT SPECTRA [J].
BLANDAMER, MJ ;
FOX, MF .
CHEMICAL REVIEWS, 1970, 70 (01) :59-+