Use of Modified Colloids and Membranes to Remove Metal Ions from Contaminated Solutions
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Titre | Use of Modified Colloids and Membranes to Remove Metal Ions from Contaminated Solutions |
Type de publication | Journal Article |
Year of Publication | 2018 |
Auteurs | Mokhter MAkmali, Magnenet C, Lakard S, Euvrard M, Aden M, Clement S, Mehdi A, Lakard B |
Journal | COLLOIDS AND INTERFACES |
Volume | 2 |
Pagination | 19 |
Date Published | JUN |
Type of Article | Article |
Mots-clés | adsorbents, chemical functionalization, hybrid silica, Interfaces, membrane filtration, Metal removal, Water treatment |
Résumé | An efficient process was developed allowing the removal of metal ions from polycontaminated aqueous solutions by combining modified colloids and membranes. Firstly, filtration experiments were performed using polyethersulfone membranes modified by a self-assembled multilayer film of polyelectrolytes. These polymer-modified membranes allowed the uptake of more than 90% of the metal ions initially present in the contaminated solutions (for solutions concentrated at 50 mg L-1). Secondly, adsorption experiments were carried out with colloidal silica encapsulated with carboxymethyl chitosan (SiO2-CMCS) or with mesoporous silica functionalized by grafting of 1,4,8,11-tetraazacyclotetradecane, i.e., cyclam (SiO2-cyclam). The adsorption capacity of these compounds was shown to be higher than numerous other literature-known adsorbents, reaching 68 and 61 mg g(-1) towards Cu(II) for SiO2-CMCS and SiO2-cyclam, respectively. Finally, by coupling adsorption with ultrafiltration in the tangential mode, the removal of Cu(II), Ni(II) and Zn(II) ions was found to be improved, allowing to reach a removal efficiency of 99% towards Cu(II), Ni(II) and Zn(II) ions at a metal concentration of 50 mg L-1, and a promising removal efficiency around 70% at a very high metal concentration of 1200 mg L-1. The mechanisms involved in the capture of the metal ions by modified membranes and colloids are also discussed. |
DOI | 10.3390/colloids2020019 |