Elution of nickel ions from alginate beads in an acid media
DOI:
https://doi.org/10.3989/revmetalm.062Keywords:
Alginate beads, Elution rate, Intrinsic kinetics, Nickel ionsAbstract
Elution of nickel ions from alginate beads was studied in a temperature range of 2 to 80 °C and a sulfuric acid concentration between 0.005 to 2.5 g L−1. The elution mechanism was established by ion exchange between nickel and ions protons, obtaining a value of 93% elution at a temperature of 80 °C and a H2SO4 concentration of 0.25 g L−1. The influence of other acids on nickel elution was also studied. The nickel elution rate was significantly influenced by temperature and concentration of H2SO4. Elution kinetics of nickel ions was studied, and the 1-(1-α)1/3=kappt model properly described the kinetics of this reaction. The dependence of nickel elution on the sulfuric acid concentration was of the order of 0.33. Moreover, the intrinsic rate constants were determined and an activation energy value of 54.5 kJ mol−1 was obtained for the temperature range studied. The results indicated that the nickel elution is a process controlled by chemical reactions.
Downloads
References
Anoop, K., Sreejalekshmi, K.G., Baiju, R.S. (2011). Nickel(II) adsorption onto biomass based activated carbon obtained from sugarcane bagasse pith. Bioresource Technol. 102 (22), 10239–10247. http://dx.doi.org/10.1016/j.biortech.2011.08.069 PMid:21924900
Aracena, A., Guajardo, N., Ib..ez, J.P., Jerez, O., Carlesi, C. (2015). Uptake of nickel ions from aqueous solutions using protonated dry alginate beads. Can. Metall. Quart. 54 (1), 58–65. http://dx.doi.org/10.1179/1879139514Y.0000000152
Belova, D.A., Lakshtanov, L.Z., Carneiro, J.F., Stipp, S.L.S. (2014). Nickel adsorption on chalk and calcite. J. Contam. Hydrol. 170, 1–9. http://dx.doi.org/10.1016/j.jconhyd.2014.09.007 PMid:25300061
Iba-ez, J.P., Umetsu, Y. (2002). Potential of protonated alginate beads for heavy metals uptake. Hydrometallurgy 64 (2), 89–99.
Iba-ez, J.P., Umetsu, Y. (2008). Uptake of Cd2+ from aqueous solutions using protonated dry alginate beads. Can. Metall. Quart. 47 (1), 45–50.
Iba-ez, J.P., Aracena, A. (2014). Uptake of Zn2+ from dilute aqueous solutions using protonated dry alginate beads. Can. Metall. Quart. 53 (1), 82–87.
Malanis, S., Katsou, E. (2013). A review of zinc and nickel adsorption on natural and modified zeolite, bentonite and vermiculite: Examination of process parameters, kinetics and isotherms. J. Hazard. Mater. 252–253, 428–461. http://dx.doi.org/10.1016/j.jhazmat.2013.03.024 PMid:23644019
O'Connell, D.W., Birkinshaw, C., O'Dwyer, T.F. (2008). Heavy metal adsorbents prepared from the modification of cellulose: A review. Bioresource Technol. 99 (15), 6709–6724. http://dx.doi.org/10.1016/j.biortech.2008.01.036 PMid:18334292
Roine, A. (1999). HSC Chemistry 6.0 Sofware, OutoKumpu Research Py, Pori, Finlandia.
Shon, H.Y., Wadsworth, M.E. (1979). Rate processes of extractive metallurgy, Plenum Press, New York, USA.
Vocciante, M., Trofa, M., Rodr.guez, P., Giraldo, L., D'Auria, T., Moreno, J.C., Erto, A. (2014). A rigorous procedure for the design of adsorption units for the removal of cadmium and nickel from process wastewaters. J. Clean. Prod. 77, 35–46. http://dx.doi.org/10.1016/j.jclepro.2013.12.001
Xia, L., Hu, Y., Zhang, B. (2014). Kinetics and equilibrium adsorption of copper(II) and nickel(II) ions from aqueous solution using sawdust xanthate modified with ethanediamine. T. Nonferr. Metal. Soc. China 24 (3), 868–875. http://dx.doi.org/10.1016/S1003-6326(14)63137-X
Published
How to Cite
Issue
Section
License
Copyright (c) 2016 Consejo Superior de Investigaciones Científicas (CSIC)

This work is licensed under a Creative Commons Attribution 4.0 International License.
© CSIC. Manuscripts published in both the printed and online versions of this Journal are the property of Consejo Superior de Investigaciones Científicas, and quoting this source is a requirement for any partial or full reproduction.All contents of this electronic edition, except where otherwise noted, are distributed under a “Creative Commons Attribution 4.0 International” (CC BY 4.0) License. You may read here the basic information and the legal text of the license. The indication of the CC BY 4.0 License must be expressly stated in this way when necessary.
Self-archiving in repositories, personal webpages or similar, of any version other than the published by the Editor, is not allowed.