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Adsorption

, Volume 25, Issue 3, pp 649–660 | Cite as

Nickel and cobalt adsorption on hydroxyapatite: a study for the de-metalation of electronic industrial wastewaters

  • Michele Ferri
  • Sebastiano Campisi
  • Antonella GervasiniEmail author
Article
  • 59 Downloads

Abstract

In the present study, the Ni(II) and Co(II) adsorption efficiency and selectivity, as well adsorption mechanisms on a stoichiometric hydroxyapatite (HAP) surface have been investigated. Characterization studies (N2 adsorption/desorption and X-ray powder diffraction (XRPD) analyses) and adsorption tests under various operative conditions provided detailed information about the use of HAP in the de-metalation of wastewaters containing Ni and Co as polluted metal species. The sorption capacity of HAP has been evaluated by static batch adsorption tests varying initial concentration of Ni(II) and Co(II) species (from ca. 0.25 to 4.3 mM), contact time (from 15 min to 24 h), and pH (from 4 to 9) operative parameters. Proposed mechanisms of adsorption of Ni(II) and Co(II) on HAP surface are ion-exchange and surface complexation; a partial contribution of chemical precipitation from bulk solution should be considered at pH 9. In addition, adsorption isotherms of Ni(II) and Co(II) on HAP have been collected at 30 °C and pH 4 and modeled by employing different equations. The maximum sorption capacities have been quantified as 0.317 mmol \({\text{g}}_{{{\text{HAP}}}}^{{ - 1}}\) (18.6 mg \({\text{g}}_{{{\text{HAP}}}}^{{ - 1}}\)) and 0.382 mmol \({\text{g}}_{{{\text{HAP}}}}^{{ - 1}}\) (22.5 mg \({\text{g}}_{{{\text{HAP}}}}^{{ - 1}}\)) for Ni(II) and Co(II), respectively. Selectivity to Co and Ni in the adsorption process on HAP has also been investigated; HAP has higher affinity towards Co than Ni species (Co:Ni = 2.5:1, molar ratio).

Keywords

Hydroxyapatite Co and Ni polluting species Adsorption isotherms Surface complexation 

Notes

Funding

Funding was provided by INAIL (Grant No. bando INAIL BRIC 2016 – ID13.)

Supplementary material

10450_2019_66_MOESM1_ESM.docx (369 kb)
Supplementary material 1 (DOCX 369 KB)

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© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Dipartimento di ChimicaUniversità degli Studi di MilanoMilanoItaly

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