TY - JOUR
T1 - Compositional dependence of the activity of nickel in silicate melts
AU - Ertel, W.
AU - Dingwell, D. B.
AU - O'Neill, H. St C.
N1 - Funding Information:
Acknowledgments--We thank Anna Dietel, Detlef Krausse, Hubert Schulze, Ralf Weigel, and Georg Herrmannsd6rfer for their technical and analytical assistance. This study has been financially supported by the DFG Schwerpunktprogramm "Experimentelle Studien tiber Elementverteilung" grant Pa-346/3-1. The manuscript benefited from the constructive comments of A. J. Naldrett, R. Nielsen, B. Mysen, and F. J. Ryerson.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1997/11
Y1 - 1997/11
N2 - The effect of melt composition on the solubility of Ni in haplobasaltic melts was investigated at 1 atm via additions of SiO2 (Quartz), Mg2SiO4 (Forsterite), and Na2SiO3 (Na-metasilicate) to the 1 atm diopside-anorthite eutectic melt composition. The experimental method applied was the mechanically assisted equilibration technique of Dingwell et al. (1994). Quenched glass samples were analyzed for major elements and Ni by the electron microprobe, and Ni was also determined in all samples by ICP-AES techniques. The Ni solubility and hence activity of NiO is not influenced by the addition of either SiO2 or Mg2SiO4 to the 1 atm anorthite-diopside eutectic composition. In contrast, addition of Na2SiO3 leads to a decrease in the Ni solubility up to 20 wt% of Na2SiO3 in the melt. Further addition results in a reversal of this trend, i.e., an increase of the Ni solubility up to about 45 wt% Na2SiO3. This observation is likely due to an exchange reaction of 2 Na for each Ca and/or Mg atom stabilizing aluminate tetrahedra in the melt structure. After all aluminate tetrahedra are stabilized by Na atoms, further addition of Na-metasilicate results in a network-modifying role of Na in the melt structure, creating new coordination possibilities for Ni. Activity coefficients for NiO in these melts have been calculated and compared with the literature. The present work leads to the conclusion that melt composition plays a minor role in determining the melt-olivine Ni partitioning. Other factors, amongst them temperature, are expected to play a much larger role.
AB - The effect of melt composition on the solubility of Ni in haplobasaltic melts was investigated at 1 atm via additions of SiO2 (Quartz), Mg2SiO4 (Forsterite), and Na2SiO3 (Na-metasilicate) to the 1 atm diopside-anorthite eutectic melt composition. The experimental method applied was the mechanically assisted equilibration technique of Dingwell et al. (1994). Quenched glass samples were analyzed for major elements and Ni by the electron microprobe, and Ni was also determined in all samples by ICP-AES techniques. The Ni solubility and hence activity of NiO is not influenced by the addition of either SiO2 or Mg2SiO4 to the 1 atm anorthite-diopside eutectic composition. In contrast, addition of Na2SiO3 leads to a decrease in the Ni solubility up to 20 wt% of Na2SiO3 in the melt. Further addition results in a reversal of this trend, i.e., an increase of the Ni solubility up to about 45 wt% Na2SiO3. This observation is likely due to an exchange reaction of 2 Na for each Ca and/or Mg atom stabilizing aluminate tetrahedra in the melt structure. After all aluminate tetrahedra are stabilized by Na atoms, further addition of Na-metasilicate results in a network-modifying role of Na in the melt structure, creating new coordination possibilities for Ni. Activity coefficients for NiO in these melts have been calculated and compared with the literature. The present work leads to the conclusion that melt composition plays a minor role in determining the melt-olivine Ni partitioning. Other factors, amongst them temperature, are expected to play a much larger role.
UR - http://www.scopus.com/inward/record.url?scp=0031391153&partnerID=8YFLogxK
U2 - 10.1016/S0016-7037(97)00356-6
DO - 10.1016/S0016-7037(97)00356-6
M3 - Article
AN - SCOPUS:0031391153
SN - 0016-7037
VL - 61
SP - 4707
EP - 4721
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 22
ER -