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Adsorption of arsenate from aqueous solution by ferric oxide-impregnated Dowex Marathon MSA anion exchange resin: application of non-linear isotherm modeling and thermodynamic studies

  • Sujitra Tandorn
  • Orn-anong ArqueropanyoEmail author
  • Wimol Naksata
  • Ponlayuth Sooksamiti
  • Ingon Chaisri
Original Article
  • 66 Downloads

Abstract

The characteristic of adsorption of As(V) onto ferric oxide-impregnated anion resin Dowex marathon MSA (FO-Dowex) was investigated. Batch adsorption experiment was studied as a function of pH, contact time, initial As(V) concentration, and temperature. The results revealed that the adsorption of As(V) onto FO-Dowex was highly pH-dependent and that the equilibrium time was attained within 360 min. Two-parameter equations (Langmuir, Freundlich, and Temkin) and three-parameter equations (Redlich–Peterson and Sips) isotherm models were used for modeling the experimental data for As(V) adsorption onto FO-Dowex at different temperatures through the non-linear regression method. The goodness of fit of the isotherm model to the experimental data was evaluated by comparing the statistical values of the coefficient of determination (R2), Chi-square (χ2) and the root mean square error (RMSE). From the isotherm analysis, the equilibrium data of As(V) adsorption onto FO-Dowex were found to be in good agreement with the Redlich–Peterson, Sips, and Langmuir isotherm model, based on the higher R2 value and the lower values of χ2 and RMSE as compared to other isotherm models. Furthermore, the calculation of thermodynamic parameters such as Gibbs free energy change (ΔG°), enthalpy change (ΔH°), and entropy change (ΔS°) revealed that the adsorption process was feasible, spontaneous, and endothermic in nature. All the results suggested that FO-Dowex could be used an effective and potential adsorbent for the removal of As(V) from aqueous solutions.

Keywords

Arsenate Adsorption Anion exchange resin Ferric oxide Isotherm Thermodynamics 

Notes

Acknowledgements

This research study was financially supported by the Development and Promotion of Science and Technology Talents Project (DPST scholarship), Thailand. The authors would like to give special thanks to the Department of Chemistry, Faculty of Science, Center of Excellence in Materials Science and Technology, and the Graduate School, Chiang Mai University, and the Department of Primary Industry and Mine Office Region 3, Chiang Mai for providing research facilities and instruments. Furthermore, the authors express their sincere thanks to the Chiang Mai University Press for proofreading this manuscript.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  • Sujitra Tandorn
    • 1
    • 2
  • Orn-anong Arqueropanyo
    • 2
    • 3
    Email author
  • Wimol Naksata
    • 2
    • 3
  • Ponlayuth Sooksamiti
    • 4
  • Ingon Chaisri
    • 2
  1. 1.Graduate SchoolChiang Mai UniversityChiang MaiThailand
  2. 2.Department of Chemistry, Faculty of ScienceChiang Mai UniversityChiang MaiThailand
  3. 3.Center of Excellence in Materials Science and TechnologyChiang Mai UniversityChiang MaiThailand
  4. 4.Office of Primary Industries and Mine, Region 3Chiang MaiThailand

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