Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 387-400 |
Seitenumfang | 14 |
Fachzeitschrift | Lithos |
Jahrgang | 80 |
Ausgabenummer | 1-4 SPEC. ISS. |
Frühes Online-Datum | 11 Nov. 2004 |
Publikationsstatus | Veröffentlicht - März 2005 |
Abstract
The aim of this experimental study was to determine the solubility of cassiterite in natural topaz- and cassiterite-bearing granite melts at temperatures close to the solidus. Profiles of Sn concentrations at glass-crystal (SnO2) interface were determined following the method of (Harrison, T.M., Watson, E.B., 1983. Kinetics of zircon dissolution and zirconium diffusion in granitic melts of variable water content. Contributions to Mineralogy and Petrology 84, 66-72). The cassiterite concentration calculated at the SnO2-glass interface is the SnO2 solubility. Experiments were performed at 700-850 °C and 2 kbar using a natural F-bearing peraluminous granitic melt with 2.8 wt.% normative corundum. Slightly H2 O-undersaturated to H2O-saturated melt compositions were chosen in order to minimize the loss of Sn to the noble element capsule walls. At the nickel-nickel oxide assemblage (Ni-NiO) oxygen fugacity buffer, the solubility of cassiterite in melts containing 1.12 wt.% F increases from 0.32 to 1.20 wt.% SnO2 with an increasing temperature from 700 to 850 °C. At the Ni-NiO buffer and a given corundum content, SnO2 solubility increases by 10% to 20% relative to an increase of F from 0 to 1.12 wt.%. SnO2 solubility increases by ∼20% relative to increasing Cl content from 0 to 0.37 wt.% in synthetic granitic melts at 850 °C. We show that Cl is at least as important as F in controlling SnO2 solubility in evolved peraluminous melts at oxygen fugacities close to the Ni-NiO buffer. In addition to the strong effects of temperature and fO2 on SnO2 solubility, an additional controlling parameter is the amount of excess Al (corundum content). At Ni-NiO and 850 °C, SnO2 solubility increases from 0.47 to 1.10 wt.% SnO2 as the normative corundum content increases from 0.1 to 2.8 wt.%. At oxidizing conditions (Ni-NiO +2 to +3), Sn is mainly incorporated as Sn4+ and the effect of excess Al seems to be significantly weaker than at reducing conditions.
ASJC Scopus Sachgebiete
- Erdkunde und Planetologie (insg.)
- Geologie
- Erdkunde und Planetologie (insg.)
- Geochemie und Petrologie
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in: Lithos, Jahrgang 80, Nr. 1-4 SPEC. ISS., 03.2005, S. 387-400.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Solubility of cassiterite in evolved granitic melts
T2 - Effect of T, fO2, and additional volatiles
AU - Bhalla, P.
AU - Holtz, Francois
AU - Linnen, R. L.
AU - Behrens, Harald
N1 - Funding Information: The authors appreciate the help of J. Koepke while conducting the electron microprobe analyses at the Institut für Mineralogie, Universität Hannover, Germany. Technical assistance was provided by Otto Dietrich. Helpful comments to the manuscript made by N. Chaudhri, A. Wittenberg, J. Webster, F. Farges, and O.T. Rämö are greatly appreciated. We are also greatly thankful for the Georg-Christoph-Lichtenberg fellowship from the Ministry of Science and Culture, Lower Saxony, Germany. Copyright: Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2005/3
Y1 - 2005/3
N2 - The aim of this experimental study was to determine the solubility of cassiterite in natural topaz- and cassiterite-bearing granite melts at temperatures close to the solidus. Profiles of Sn concentrations at glass-crystal (SnO2) interface were determined following the method of (Harrison, T.M., Watson, E.B., 1983. Kinetics of zircon dissolution and zirconium diffusion in granitic melts of variable water content. Contributions to Mineralogy and Petrology 84, 66-72). The cassiterite concentration calculated at the SnO2-glass interface is the SnO2 solubility. Experiments were performed at 700-850 °C and 2 kbar using a natural F-bearing peraluminous granitic melt with 2.8 wt.% normative corundum. Slightly H2 O-undersaturated to H2O-saturated melt compositions were chosen in order to minimize the loss of Sn to the noble element capsule walls. At the nickel-nickel oxide assemblage (Ni-NiO) oxygen fugacity buffer, the solubility of cassiterite in melts containing 1.12 wt.% F increases from 0.32 to 1.20 wt.% SnO2 with an increasing temperature from 700 to 850 °C. At the Ni-NiO buffer and a given corundum content, SnO2 solubility increases by 10% to 20% relative to an increase of F from 0 to 1.12 wt.%. SnO2 solubility increases by ∼20% relative to increasing Cl content from 0 to 0.37 wt.% in synthetic granitic melts at 850 °C. We show that Cl is at least as important as F in controlling SnO2 solubility in evolved peraluminous melts at oxygen fugacities close to the Ni-NiO buffer. In addition to the strong effects of temperature and fO2 on SnO2 solubility, an additional controlling parameter is the amount of excess Al (corundum content). At Ni-NiO and 850 °C, SnO2 solubility increases from 0.47 to 1.10 wt.% SnO2 as the normative corundum content increases from 0.1 to 2.8 wt.%. At oxidizing conditions (Ni-NiO +2 to +3), Sn is mainly incorporated as Sn4+ and the effect of excess Al seems to be significantly weaker than at reducing conditions.
AB - The aim of this experimental study was to determine the solubility of cassiterite in natural topaz- and cassiterite-bearing granite melts at temperatures close to the solidus. Profiles of Sn concentrations at glass-crystal (SnO2) interface were determined following the method of (Harrison, T.M., Watson, E.B., 1983. Kinetics of zircon dissolution and zirconium diffusion in granitic melts of variable water content. Contributions to Mineralogy and Petrology 84, 66-72). The cassiterite concentration calculated at the SnO2-glass interface is the SnO2 solubility. Experiments were performed at 700-850 °C and 2 kbar using a natural F-bearing peraluminous granitic melt with 2.8 wt.% normative corundum. Slightly H2 O-undersaturated to H2O-saturated melt compositions were chosen in order to minimize the loss of Sn to the noble element capsule walls. At the nickel-nickel oxide assemblage (Ni-NiO) oxygen fugacity buffer, the solubility of cassiterite in melts containing 1.12 wt.% F increases from 0.32 to 1.20 wt.% SnO2 with an increasing temperature from 700 to 850 °C. At the Ni-NiO buffer and a given corundum content, SnO2 solubility increases by 10% to 20% relative to an increase of F from 0 to 1.12 wt.%. SnO2 solubility increases by ∼20% relative to increasing Cl content from 0 to 0.37 wt.% in synthetic granitic melts at 850 °C. We show that Cl is at least as important as F in controlling SnO2 solubility in evolved peraluminous melts at oxygen fugacities close to the Ni-NiO buffer. In addition to the strong effects of temperature and fO2 on SnO2 solubility, an additional controlling parameter is the amount of excess Al (corundum content). At Ni-NiO and 850 °C, SnO2 solubility increases from 0.47 to 1.10 wt.% SnO2 as the normative corundum content increases from 0.1 to 2.8 wt.%. At oxidizing conditions (Ni-NiO +2 to +3), Sn is mainly incorporated as Sn4+ and the effect of excess Al seems to be significantly weaker than at reducing conditions.
KW - Cassiterite
KW - Cl
KW - Concentration
KW - F
KW - Granite
KW - SnO solubility
UR - http://www.scopus.com/inward/record.url?scp=13244249613&partnerID=8YFLogxK
U2 - 10.1016/j.lithos.2004.06.014
DO - 10.1016/j.lithos.2004.06.014
M3 - Article
AN - SCOPUS:13244249613
VL - 80
SP - 387
EP - 400
JO - Lithos
JF - Lithos
SN - 0024-4937
IS - 1-4 SPEC. ISS.
ER -