Nanofiltration (NF)-like membranes have shown potential
for implementing
forward osmosis (FO) for resource recovery. Despite the popular use
of poly(allylamine hydrochloride) (PAH) as a polycation in the layer-by-layer
(LbL) coating of NF-like membranes, it remained ambiguous whether
substantial changes could result from the minor structural difference
in polyamine when employing polyvinylamine (PVAm) as the polycation.
This study systematically assessed the filtration capability of the
NF-like membranes with varying combinations of the PAH- and PVAm-containing
bilayers in an FO process. The FO experiments revealed that the dominance
of PVAm-containing bilayers in the upper part of the active layer
could result in decreases in both the water permeability and the rejection
of divalent salts. Subsequent fouling tests demonstrated that the
membrane coated solely with PVAm-containing bilayers (i.e., the VVV
membrane) exhibited the fastest flux decline in the fouling tests
with sodium alginate (SA), whereas the fouling layer could be more
easily removed by the crossflow. Optical coherence tomography (OCT)
characterization indicated that the bridging effect of divalent cations
could promote the aggregation of SA to form a particulate layer more
susceptible to the shear effect. All the results shed light on the
improvement of NF-like FO by regulating the formation of the active
layer via the LbL assembly.