An XAS study of molybdenum speciation in hydrothermal chloride solutions from 25-385°C and 600 bar

被引:55
作者
Borg, Stacey [1 ,4 ]
Liu, Weihua [1 ]
Etschmann, Barbara [2 ]
Tian, Yuan [3 ,5 ]
Brugger, Joel [2 ,3 ]
机构
[1] CSIRO Earth Sci & Resource Engn, Clayton, Vic 3168, Australia
[2] Univ Adelaide, Sch Earth & Environm Sci, Ctr Tecton Resources & Explorat TRaX, Adelaide, SA 5005, Australia
[3] S Australian Museum, Dept Mineral, Adelaide, SA 5000, Australia
[4] Univ Tasmania, CODES Ctr Excellence, Hobart, Tas, Australia
[5] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
基金
澳大利亚研究理事会;
关键词
X-RAY-ABSORPTION; CRYSTAL-STRUCTURE; THERMODYNAMIC PROPERTIES; DEGREES-C; AQUEOUS-SOLUTIONS; METAL-COMPLEXES; ACIDIC-SOLUTION; WATER-VAPOR; SOLUBILITY; FLUID;
D O I
10.1016/j.gca.2012.06.001
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
Molybdenum(VI) is expected to be the main form of Mo in hydrothermal fluids up to magmatic hydrothermal conditions. We conducted an in situ X-ray absorption spectroscopic study of Mo(VI) speciation in H2O-HCl-NaCl brines up to 385 degrees C at a pressure of 600 bar. The EXAFS (Extended X-ray Absorption Fine Structure) and XANES (X-ray Absorption Near-Edge Structure) data supported by ab-initio XANES calculations confirm that tetrahedral complexes containing the molybdate anion (MoO42-) predominate in basic to near neutral solutions with chloride concentration up to 5.5 m. The geometry of this species changes little over the investigated P-T range, and there is no complexation between MoO42- and chloride. In highly acidic solutions, Mo(VI) speciation is dominated by distorted octahedral oxo-chloro complexes MoOmCln6-2m-n; the number of chloride ligands increases with increasing temperature, to a maximum of similar to 5 (e. g., MoOCl5-) at 340 degrees C in 6.21 m HCl. These data suggest that Mo speciation is dominated by tetrahedral molybdate species (e. g., HMoO4- or MoO42-) in the basic to near neutral solution phase of natural hydrothermal fluid, and chloride complexes will only play a significant role in highly acidic fluid under our experimental P-T conditions. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:292 / 307
页数:16
相关论文
共 66 条
[1]   ON THE CRYSTAL STRUCTURE OF MOLYBDENUM TRIOXIDE [J].
ANDERSSON, G ;
MAGNELI, A .
ACTA CHEMICA SCANDINAVICA, 1950, 4 (05) :793-797
[2]  
[Anonymous], 1989, GEOKHIMIYA+
[3]   SPECTRAL AND STRUCTURAL STUDIES OF SOME GROUP 6A DIOXYDIHALIDES [J].
BARRACLOUGH, CG ;
STALS, J .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1966, 19 (05) :741-+
[4]   NEUTRON POWDER DIFFRACTION STUDY OF MOLYBDENUM AND TUNGSTEN DIOXIDES [J].
BOLZAN, AA ;
KENNEDY, BJ ;
HOWARD, CJ .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1995, 48 (08) :1473-1477
[5]   A REFINEMENT OF CRYSTAL STRUCTURE OF MOLYBDENUM DIOXIDE [J].
BRANDT, BG ;
SKAPSKI, AC .
ACTA CHEMICA SCANDINAVICA, 1967, 21 (03) :661-&
[6]   An XAS study of the structure and thermodynamics of Cu(I) chloride complexes in brines up to high temperature (400 °C, 600 bar) [J].
Brugger, J. ;
Etschmann, B. ;
Liu, W. ;
Testemale, D. ;
Hazemann, J. L. ;
Emerich, H. ;
van Beek, W. ;
Proux, O. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2007, 71 (20) :4920-4941
[7]   Probing ore deposits formation: New insights and challenges from synchrotron and neutron studies [J].
Brugger, Joel ;
Pring, Allan ;
Reith, Frank ;
Ryan, Chris ;
Etschmann, Barbara ;
Liu, Weihua ;
O'Neill, Brian ;
Ngothai, Yung .
RADIATION PHYSICS AND CHEMISTRY, 2010, 79 (02) :151-161
[8]   High SO2 flux, sulfur accumulation, and gas fractionation at an erupting submarine volcano [J].
Butterfield, David A. ;
Nakamura, Ko-ichi ;
Takano, Bokuichiro ;
Lilley, Marvin D. ;
Lupton, John E. ;
Resing, Joseph A. ;
Roe, Kevin K. .
GEOLOGY, 2011, 39 (09) :803-806
[9]   THE PARTITIONING OF COPPER AND MOLYBDENUM BETWEEN SILICATE MELTS AND AQUEOUS FLUIDS [J].
CANDELA, PA ;
HOLLAND, HD .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1984, 48 (02) :373-380
[10]  
Capitelli F, 2006, ASIAN J CHEM, V18, P2856