Layer-by-layer (LbL) assembly of the alternating adsorption
of
oppositely charged polyions is an extensively studied method to produce
nanofiltration membranes. In this work, the concept of chaotropicity
of the polycation and its counterion is introduced in the LbL field.
In general, the more chaotropic a polyion, the lower its effective
charge, charge availability, and hydrophilicity. Here, this is researched
for the well-known PDADMAC (polydiallyldimethylammonium chloride)
and PAH (poly(allylamine) hydrochloride), and the synthesized PAMA
(polyallylmultimethylammonium), with two different counterions (I– and Cl–). Higher chaotropicity (PDADMAC
> PAMA-I > PAMA-Cl > PAH) translates into a reduced charge
availability
and a more pronounced extrinsic charge compensation, resulting in
more mass adsorption and a higher pure water permeability. PAMA-containing
membranes show the most interesting results in the series. Due to
its molecular structure, the chaotropicity of this polycation perfectly
lies between PDADMAC and PAH. Overall, the chaotropicity of PAMA membranes
allows for the formation of the right balance between extrinsic and
intrinsic charge compensation with PSS. Moreover, modifying the nature
of the counterions of PAMA (I– or Cl–) allows to tune the density of the multilayer and results in lower
size exclusion abilities with PAMA-I compared to PAMA-Cl (higher MWCO
and lower MgSO4 retention). In general, the contextualization
of the polyion interaction within the specific (poly)ion effects expands
the understanding of the influence of the charge density of polycations
without ignoring the chemical nature of the functional groups in their
monomer units.