Rare earth elements sorption to iron oxyhydroxide: Model development and application to groundwater

Iron oxyhydroxides are among the most important colloids that control rare earth elements (REE) concentrations and transport in natural hydrosystems. In this study, REE surface complexation to iron oxyhydroxides (Fe(OH)3(a)) was described by using the Donnan diffuse layer model and a two-site (i.e....

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Published inApplied geochemistry Vol. 87; pp. 158 - 166
Main Authors Liu, Haiyan, Pourret, Olivier, Guo, Huaming, Bonhoure, Jessica
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.12.2017
Elsevier
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Abstract Iron oxyhydroxides are among the most important colloids that control rare earth elements (REE) concentrations and transport in natural hydrosystems. In this study, REE surface complexation to iron oxyhydroxides (Fe(OH)3(a)) was described by using the Donnan diffuse layer model and a two-site (i.e. ≡FesOH and ≡FewOH) model. The specific surface area and pH of zero charge were fixed as 100000 m2/mol and 8.0, respectively. The surface site density for weak and strong binding sites were fixed at 0.1 moL/mol Fe (≡FewOH) and 0.001 moL/mol Fe (≡FesOH) respectively. The two site types were used with pKa1int = 7.29 and pKa2int = 8.93. Using linear free energy relationship, the estimated equilibrium surface complexation constants (log K) increased from light REE (LREE) to heavy REE (HREE). Results of REE modeling calculation using the determined log K revealed a good fit of experimental data, showing an order of sorption on iron oxyhydroxides: HREE > MREE > LREE and preferential sorption of HREE at a lower pH. However, sorption edges only showed a slight change with ionic strength (0.1–0.7 moL/L) for the whole REE series. The generalized model was subsequently used to evaluate the impact of iron oxyhydroxides on REE speciation in groundwater. Application of the model to “model groundwater” showed that iron oxyhydroxide complexes of REE were significant in near neutral and weakly alkaline pH. This study contributes to putting forward a comprehensive database which would be useful for the application of surface complexation model to describe REE sorption by amorphous ferric hydroxides in nature. [Display omitted] •Modeling study of the REE sorption onto iron oxyhydroxide is proposed.•Binding was described using two sites Donnan diffuse layer.•Heavy REE show a greater affinity for iron oxyhydroxide than light REE and middle REE.•Modeling suggests a preferential accumulation of Ce on solid phase than its neighboring La and Pr.•The proposed model is able to predict the impact of iron oxyhydroxide on REE in nature.
AbstractList Iron oxyhydroxides are among the most important colloids that control rare earth elements (REE) concentrations and transport in natural hydrosystems. In this study, REE surface complexation to iron oxyhydroxides (Fe(OH)3(a)) was described by using the Donnan diffuse layer model and a two-site (i.e. ≡FeˢOH and ≡FeʷOH) model. The specific surface area and pH of zero charge were fixed as 100000 m²/mol and 8.0, respectively. The surface site density for weak and strong binding sites were fixed at 0.1 moL/mol Fe (≡FeʷOH) and 0.001 moL/mol Fe (≡FeˢOH) respectively. The two site types were used with pKa1ⁱⁿᵗ = 7.29 and pKa2ⁱⁿᵗ = 8.93. Using linear free energy relationship, the estimated equilibrium surface complexation constants (log K) increased from light REE (LREE) to heavy REE (HREE). Results of REE modeling calculation using the determined log K revealed a good fit of experimental data, showing an order of sorption on iron oxyhydroxides: HREE > MREE > LREE and preferential sorption of HREE at a lower pH. However, sorption edges only showed a slight change with ionic strength (0.1–0.7 moL/L) for the whole REE series. The generalized model was subsequently used to evaluate the impact of iron oxyhydroxides on REE speciation in groundwater. Application of the model to “model groundwater” showed that iron oxyhydroxide complexes of REE were significant in near neutral and weakly alkaline pH. This study contributes to putting forward a comprehensive database which would be useful for the application of surface complexation model to describe REE sorption by amorphous ferric hydroxides in nature.
Iron oxyhydroxides are among the most important colloids that control rare earth elements (REE) concentrations and transport in natural hydrosystems. In this study, REE surface complexation to iron oxyhydroxides (Fe(OH)3(a)) was described by using the Donnan diffuse layer model and a two-site (i.e. ≡FesOH and ≡FewOH) model. The specific surface area and pH of zero charge were fixed as 100000 m2/mol and 8.0, respectively. The surface site density for weak and strong binding sites were fixed at 0.1 moL/mol Fe (≡FewOH) and 0.001 moL/mol Fe (≡FesOH) respectively. The two site types were used with pKa1int = 7.29 and pKa2int = 8.93. Using linear free energy relationship, the estimated equilibrium surface complexation constants (log K) increased from light REE (LREE) to heavy REE (HREE). Results of REE modeling calculation using the determined log K revealed a good fit of experimental data, showing an order of sorption on iron oxyhydroxides: HREE > MREE > LREE and preferential sorption of HREE at a lower pH. However, sorption edges only showed a slight change with ionic strength (0.1–0.7 moL/L) for the whole REE series. The generalized model was subsequently used to evaluate the impact of iron oxyhydroxides on REE speciation in groundwater. Application of the model to “model groundwater” showed that iron oxyhydroxide complexes of REE were significant in near neutral and weakly alkaline pH. This study contributes to putting forward a comprehensive database which would be useful for the application of surface complexation model to describe REE sorption by amorphous ferric hydroxides in nature. [Display omitted] •Modeling study of the REE sorption onto iron oxyhydroxide is proposed.•Binding was described using two sites Donnan diffuse layer.•Heavy REE show a greater affinity for iron oxyhydroxide than light REE and middle REE.•Modeling suggests a preferential accumulation of Ce on solid phase than its neighboring La and Pr.•The proposed model is able to predict the impact of iron oxyhydroxide on REE in nature.
Author Pourret, Olivier
Liu, Haiyan
Guo, Huaming
Bonhoure, Jessica
Author_xml – sequence: 1
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  givenname: Olivier
  surname: Pourret
  fullname: Pourret, Olivier
  email: olivier.pourret@unilasalle.fr
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  givenname: Huaming
  surname: Guo
  fullname: Guo, Huaming
  organization: State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Beijing), Beijing 100083, PR China
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  givenname: Jessica
  surname: Bonhoure
  fullname: Bonhoure, Jessica
  organization: UniLaSalle, AGHYLE, 60026 Beauvais Cedex, France
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Keywords Sorption
Rare earth elements
Groundwater
Iron oxyhydroxides
Surface complexation modeling
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Snippet Iron oxyhydroxides are among the most important colloids that control rare earth elements (REE) concentrations and transport in natural hydrosystems. In this...
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SubjectTerms binding sites
colloids
Earth Sciences
ferric hydroxide
Geochemistry
Gibbs free energy
Groundwater
ionic strength
iron
Iron oxyhydroxides
Rare earth elements
Sciences of the Universe
Sorption
surface area
Surface complexation modeling
Title Rare earth elements sorption to iron oxyhydroxide: Model development and application to groundwater
URI https://dx.doi.org/10.1016/j.apgeochem.2017.10.020
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https://hal.science/hal-02136360
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