Molecular details and free energy barriers of ion de-coordination at elevated salinity and pressure and their consequences for membrane separations
Ion dehydration has been hypothesized to strongly influence separation performance in membrane systems and ion transport in nanoscale channels. However, the molecular details of ion dehydration in membranes are not well understood, in particular under the high pressures and concentrations required for brine treatment. In this study, we define \textit{de-coordination} as the process by which an ion decreases its total coordination number, including both water molecules and counterions. We estimate the de-coordination free energies in bulk solution for a range of different ions at high pressure and salinity relevant to brine treatment using molecular simulation. We also propose alternatives to the coordination number as the size constraint for traversing nanoscale constrictions, such as the maximum cross-sectional area of the complexed ion. We show that high operating pressures do not significantly change cation hydration shell stability nor the shell size, while high ionic concentrations lower the free energy barrier to reduce the cation coordination number. We find that anion de-coordination free energies are largely unaffected by elevated salinity and pressure conditions. Finally, we discuss the implications on ion-ion selectivity in separations membranes (e.g. extracting lithium from salt-lake brines) due to the effects of elevated pressure and salinity on ion de-coordination.