The
surface properties and structure of a membrane play a significant
role in the ion selectivity during electrodialysis. Recently, polydopamine
(PDA) and its related nanomaterials have emerged as promising materials
to develop composite membranes for higher separation requirements.
Previous research has shown that the codeposition of PDA and polyethylenimine
(PEI) triggered by Cu2+/H2O2 could
facilitate the transport of H+ while rejecting multivalent
ions though electrostatic effects. However, the enhanced H+ flux by acid–base pairs is not applicable in a Na+/Mg2+ system. Here we report a facile method to construct
monovalent selective membranes through rapid codeposition of PDA/PEI
and Mil(53)-Al, followed by cross-linking with trimesoyl chloride
(TMC). The positive −NH2 allows us to reject multivalent
cations, while porous Mil(53)-Al can accelerate the migration of Na+. The surface morphology and physicochemical properties of
the as-prepared composite membranes were studied by SEM, AFM, and
XPS analyses, and the electrochemical properties were evaluated by
EIS and current–voltage curves. The results demonstrated that
a robust skin layer was formed on the commercial cation exchange membrane
substrate, endowing the ion-exchange membrane with an increased separation
performance for multivalent ions. The monovalent selectivity and ion
flux can be tuned by changing the ratio of Mil(53)-Al during the codeposition
process. A mass ratio of 0.2–0.4% (w/v) for Mil(53)-Al is the
optimum protocol, yielding a membrane with a permselectivity of about
0.3 and an ion flux of about 22.0 and 0.6 mol·cm–2·s–1 for Na+ and Mg2+, respectively. At this condition, the PDA-coated membrane maintains
a high monovalent selectivity with enhanced Na+ and Mg2+ flux in single salt solutions. This one-pot method to prepare
PDA based membrane provides a new direction to prepare monovalent
selective ion-exchange membranes.