ENSICAEN, Laboratoire de Chimie Moléculaire et Thioorganique (LCMT), Laboratoire associé au CNRS, UMR6507, 6 Boulevard du Maréchal Juin, 14000 Caen, France
Prof. Dr. Didier Villemin
ENSICAEN, Laboratoire de Chimie Moléculaire et Thioorganique (LCMT), Laboratoire associé au CNRS, UMR6507, 6 Boulevard du Maréchal Juin, 14000 Caen, France
A new sorbent, the polyethylenimine methylenephosphonic acid (PEIMPA), was synthesized from commercially available polyethylenimine. After characterization by (1H, 13C, 31P) NMR, elementary analysis, UV/VIS and FTIR, the new ion exchange polymer PEIMPA has been investigated in liquid – solid extraction of a mixture of Cd(II), Co(II), Cu(II), Fe(III), Ni(II), Pb(II), and Zn(II) cations from a mineral residue of zinc ore dissolved in nitric acid. The selectivity of this polymer was studied as a function of pH. PEIMPA can sorb much higher amounts of Fe ion than Cd, Co, Cu, Ni, Pb, and Zn ions. The recovery of Fe(III) is almost quantitative. Because of this remarkable affinity, the PEIMPA resin has the potential for application in several fields. Further studies of the polymer are in progress.
The chemical and physical properties of imidazolium-based ionic liquids are determined by the interactions between the counter-ions. The C(2) position plays an important role in these interactions, as it represents the predominant site for interionic hydrogen bonding. This study shows that the directional hydrogen bonds between highly symmetrical anions (iodide, tetrafluoroborate, hexafluorophosphate) and the C(2)-H group of the 1-methyl-3-propylimidazolium cation determine the molecular and macroscopic behavior in terms of the thermal properties. Upon replacing the C(2) proton by a methyl group, the anion repositions itself at the C(4)/(5) moiety, where it forms a new hydrogen bond, apparently with only one of the two CH groups. In addition, the larger the anion is in diameter, the more likely it will establish further interactions with other parts of the cation, such as the propyl chain.