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Sorption of Ni by birnessite: equilibrium controls on Ni in seawater

Sorption of Ni by birnessite: equilibrium controls on Ni in seawater
Sorption of Ni by birnessite: equilibrium controls on Ni in seawater
Synthetic hexagonal birnessite (Hx-birnessite) is a close analogue to natural poorly crystalline phyllomanganate phases found in soils and marine ferromanganese deposits. These phases are often highly enriched in trace metals such as Ni and Co. We measured the sorption of Ni(II) onto synthetic hexagonal birnessite (Hx-birnessite) from pH 1 to 7. EXAFS spectra show that, at pH 3.7, Ni is adsorbed to the Hx-birnessite surface above vacancy sites on {001} as a tridentate corner-sharing complex. We developed a surface complexation model for Ni adsorption based on the equilibria

3(?Mn2O? 2/3) + Ni+ 2 = (?Mn2O)3Ni0



3(?Mn2O? 2/3) + Ni+ 2 + H2O = (?Mn2O)3Ni(OH)? + H+


Using this surface complexation model, we predict the concentration of Ni in seawater in equilibrium with Ni-bearing birnessite found in hydrogenetic FeMn crusts and nodules. Our predicted results are in good agreement with observed Ni concentrations in seawater and suggest that the concentration of dissolved Ni in seawater is buffered by sorption to birnessite or a related MnO2 phase. However, in addition to the surface complex, Ni also sorbs by structural incorporation into the vacancy site. In our synthetic samples at pH 7, EXAFS shows 10% of Ni is structurally incorporated into Hx-birnessite. In natural birnessites found in marine ferromanganese crusts and nodules, EXAFS shows that all of the sorbed Ni is structurally incorporated. Structural incorporation suggests that Ni sorption may be irreversible.
nickel, hexagonal birnessite, adsorption, exafs spectroscopy, surface complexation modelling
0009-2541
94-106
Peacock, Caroline L.
8a178011-0d4c-4fc3-867e-9883488c271f
Sherman, David M.
118a3a93-b048-4346-92a9-3509991bcffe
Peacock, Caroline L.
8a178011-0d4c-4fc3-867e-9883488c271f
Sherman, David M.
118a3a93-b048-4346-92a9-3509991bcffe

Peacock, Caroline L. and Sherman, David M. (2007) Sorption of Ni by birnessite: equilibrium controls on Ni in seawater. Chemical Geology, 238 (1-2), 94-106. (doi:10.1016/j.chemgeo.2006.10.019).

Record type: Article

Abstract

Synthetic hexagonal birnessite (Hx-birnessite) is a close analogue to natural poorly crystalline phyllomanganate phases found in soils and marine ferromanganese deposits. These phases are often highly enriched in trace metals such as Ni and Co. We measured the sorption of Ni(II) onto synthetic hexagonal birnessite (Hx-birnessite) from pH 1 to 7. EXAFS spectra show that, at pH 3.7, Ni is adsorbed to the Hx-birnessite surface above vacancy sites on {001} as a tridentate corner-sharing complex. We developed a surface complexation model for Ni adsorption based on the equilibria

3(?Mn2O? 2/3) + Ni+ 2 = (?Mn2O)3Ni0



3(?Mn2O? 2/3) + Ni+ 2 + H2O = (?Mn2O)3Ni(OH)? + H+


Using this surface complexation model, we predict the concentration of Ni in seawater in equilibrium with Ni-bearing birnessite found in hydrogenetic FeMn crusts and nodules. Our predicted results are in good agreement with observed Ni concentrations in seawater and suggest that the concentration of dissolved Ni in seawater is buffered by sorption to birnessite or a related MnO2 phase. However, in addition to the surface complex, Ni also sorbs by structural incorporation into the vacancy site. In our synthetic samples at pH 7, EXAFS shows 10% of Ni is structurally incorporated into Hx-birnessite. In natural birnessites found in marine ferromanganese crusts and nodules, EXAFS shows that all of the sorbed Ni is structurally incorporated. Structural incorporation suggests that Ni sorption may be irreversible.

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More information

Published date: 15 March 2007
Keywords: nickel, hexagonal birnessite, adsorption, exafs spectroscopy, surface complexation modelling

Identifiers

Local EPrints ID: 44637
URI: http://eprints.soton.ac.uk/id/eprint/44637
ISSN: 0009-2541
PURE UUID: c09fe020-6776-445d-a0d0-db82f64cfedc

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Date deposited: 05 Mar 2007
Last modified: 15 Mar 2024 09:06

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Contributors

Author: Caroline L. Peacock
Author: David M. Sherman

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