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Journal of Applied Sciences

Year: 2010 | Volume: 10 | Issue: 8 | Page No.: 599-610
DOI: 10.3923/jas.2010.599.610

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Authors


D.W. Nyembe


B.B. Mamba


A.F. Mulaba-Bafubiandi


Keywords


  • ion-exchange
  • Co2+ solutions
  • Cu2+
  • Clinoptilolite
  • isotherms
  • kinetics
Research Article

Adsorption Mechanisms of Co2+ and Cu2+ from Aqueous Solutions using Natural Clinoptilolite: Equilibrium and Kinetic Studies

D.W. Nyembe, B.B. Mamba and A.F. Mulaba-Bafubiandi
The study was aimed at determining the adsorption mechanisms involved in the ion-exchange of Co2+ and Cu2+ in their aqueous solutions using Southern African natural clinoptilolite in its original (non-activated form). The clinoptilolite was characterized with FTIR and XRF and was found to consist of quartz, alumino-silicates calcite and dolomite was shown to be effective at removing Co2+ and Cu2+ ions from an aqueous solution. Both Co2+ and Cu2+ were readily adsorbed from dilute solutions (0.0020 M) followed by a 0.0698 M solution and the least removal was recorded with 0.2000 M solution. After mixing Co2+ and Cu2+ to generate a mixed Co/Cu synthetic solution the removal rates variable results and depended on the salt concentration ratios of the mixed solution. It was observed that Co2+ was generally easily removed from these solutions compared to Cu2+. The adsorption data of the metal ions were postulated by Langmuir and Freundlich isotherms over the entire concentration range. Kinetic data for adsorption kinetics accurately fitted the pseudo-first order with external diffusion models indicating that the ion-exchange of Co2+ and Cu2+ ions could be happening on the exterior surface of the sorbent while the contribution of internal diffusion mechanism was considered to be minimal.
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How to cite this article

D.W. Nyembe, B.B. Mamba and A.F. Mulaba-Bafubiandi, 2010. Adsorption Mechanisms of Co2+ and Cu2+ from Aqueous Solutions using Natural Clinoptilolite: Equilibrium and Kinetic Studies. Journal of Applied Sciences, 10: 599-610.

DOI: 10.3923/jas.2010.599.610

URL: https://scialert.net/abstract/?doi=jas.2010.599.610

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