A comparative study on selective adsorption of metal ions using aminated adsorbents

[Display omitted] ► Aminated adsorbents are compared in multicomponent adsorptions of metal ions. ► NH2-MCM-41 shows superior adsorption selectivity performance. ► Chitosan shows selectivity for Cu2+ in multicomponent systems but not Ni–Zn system. It is well-known that chitosan consists of amino gro...

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Veröffentlicht in:Journal of colloid and interface science 2013-04, Vol.395, p.230-240
Hauptverfasser: Koong, Len Foong, Lam, Koon Fung, Barford, John, McKay, Gordon
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] ► Aminated adsorbents are compared in multicomponent adsorptions of metal ions. ► NH2-MCM-41 shows superior adsorption selectivity performance. ► Chitosan shows selectivity for Cu2+ in multicomponent systems but not Ni–Zn system. It is well-known that chitosan consists of amino groups for the chelation of metal ions while NH2-MCM-41 has excellent adsorption selectivities for metals. This work compares both adsorption capacities and selectivities of chitosan and NH2-MCM-41. It has been found that chitosan has adsorption capacities of 1.76mmol/g, 1.03mmol/g and 1.30mmol/g for Cu2+, Ni2+ and Zn2+ respectively whereas NH2-MCM-41 has adsorption capacity of 1.52mmol/g, 0.8mmol/g and 0.83mmol/g for Cu2+, Ni2+ and Zn2+. The higher adsorption capacity in chitosan is attributed to its higher loading of amine groups. The single component adsorption isotherms were well-fitted using Freundlich model. The binary adsorptions of Cu2+–Zn2+ and Ni2+–Zn2+ systems showed similar adsorption selectivities for both adsorbents. However, chitosan has no preferential adsorption for Ni2+–Zn2+ system while NH2-MCM-41 has a good selectivity towards Zn2+. It is believed that the difference can be attributed to the heterogeneous surface of chitosan due to its organic nature. The multi-component adsorptions were best described by a multicomponent extended Freundlich model. Despite the surface functional group, this work indicates the importance of the adsorbent support on selective adsorption.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2012.12.047