The self-diffusion coefficient, the spin-lattice relaxation times and ionic conductivity of lithium ions in liq-uid mixtures composed of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP)have been thoroughly investigated as a function of composition and temperature by NMR spectroscopyand conductometry. While the temperature and composition dependence of diffusion coefficients oflithium ions follow the same trend observed for those of the surfactant molecules, the spin-lattice relax-ation times of lithium ions and1H are remarkably different. The observed behavior has been interpretedin terms of lithium ions diffusion occurring through its association with the negatively charged HDEHPspecies, whereas its rotational dynamics being decoupled from that of surfactant molecules, gives T1val-ues lower than those of surfactant molecules and characterized by a different temperature dependence.
Bis(2-ethylhexyl)phosphoric acid/bis(2-ethylhexyl)amine mixtures as solvent media for lithium-ions: a dynamical study
NICOTERA, ISABELLA;OLIVIERO ROSSI, Cesare
;C. Simari;
2016-01-01
Abstract
The self-diffusion coefficient, the spin-lattice relaxation times and ionic conductivity of lithium ions in liq-uid mixtures composed of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP)have been thoroughly investigated as a function of composition and temperature by NMR spectroscopyand conductometry. While the temperature and composition dependence of diffusion coefficients oflithium ions follow the same trend observed for those of the surfactant molecules, the spin-lattice relax-ation times of lithium ions and1H are remarkably different. The observed behavior has been interpretedin terms of lithium ions diffusion occurring through its association with the negatively charged HDEHPspecies, whereas its rotational dynamics being decoupled from that of surfactant molecules, gives T1val-ues lower than those of surfactant molecules and characterized by a different temperature dependence.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.