Selective Lanthanides Sequestration Based on a Self-Assembled Organosilica

In this paper, we investigate the cation-exchange properties of a self-assembled hybrid material towards trivalent ions, lanthanides (La3+, Eu3+, Gd3+, Yb3+) and Fe3+. The bis-zwitterionic lamellar material was prepared by sol-gel process from only 3-aminopropyltriethoxysilane (APTES), succinic anhydride, and ethylenediamine. In ethanol heated under reflux, the exchange ethylenediammonium versus Ln(3+) proved to be complete by complexometry measurements and elemen-tal analyses, one Cl- ion per one Ln(III) remaining as expected for charge balance. In aqueous solution at 20 degrees C, the material was found to be selective towards lanthanide in spite of the similarity of their ionic radii. The cation uptake depends on the nature of the salt, the difference between two lanthanides reaching up to 20% in some cases. Finally, ion-exchange reaction with FeCl3 was chosen as a probe to get more information on the material after incorporation of trivalent ions. Based on Mossbauer spectroscopic investigations on the resulting material in conjunction with the XRD analysis of materials containing trivalent ions, a structural model was proposed to describe the incorporation of trivalent ions by exchange reaction within the original zwitterionic material.