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Herein, we present a systematic investigation of the impact of silica nanoparticle (SiNP) size and surface chemistry on the nanoparticle dispersion state and the resulting morphology and vanadium ion permeability of the composite ionomer membranes. Specifically, Nafion containing a mass fraction of 5% silica particles, ranging in nominal diameters from 10 nm to >1 μm and with both sulfonic acid- and amine-functionalized surfaces, was fabricated. Most notably, an 80% reduction in vanadium ion permeability was observed for ionomer membranes containing amine-functionalized SiNPs at a nominal diameter of 200 nm. Further, these membranes exhibited an almost 400% increase in proton selectivity when compared to pristine Nafion. Trends in vanadium ion permeability within a particular nominal diameter were seen to be a function of the surface chemistry, where, for example, vanadyl ion permeability was observed to increase with increasing particle size for membranes containing unfunctionalized SiNPs, while it was seen to remain relatively constant for membranes containing amine-functionalized SiNPs. In general, the silica particles tended to exhibit a higher extent of aggregation as the size of the particles was increased. From small-angle neutron scattering experiments, an increase in the spacing of the hydrophobic domains was observed for all composite membranes, though particle size and surface chemistry were seen to have varying impacts on the spacing of the ionic domains of the ionomer. 

Herein, a series of novel, lignin-based hydrogel composites was fabricated by incorporating ultraclean lignins (UCLs), of controlled molecular weight and low dispersity, into poly(vinyl alcohol) (PVA). The UCLs were obtained from a novel liquid–liquid fractionation of high dispersity crude bulk lignins (CBLs) obtained from Kraft black liquor. A complementary series of composite hydrogels was fabricated using these CBLs. Both the CBLs and UCLs were functionalized with vinyl-containing acrylate groups allowing the lignins to chemically crosslink with themselves, forming an interpenetrated network with the thermally-crosslinked network of PVA chains. Successful functionalization of the UCLs was demonstrated by proton and phosphorous nuclear magnetic resonance. PVA–lignin hydrogels containing 20 wt% UCL saw a reduction in methylene blue (MB) permeability by approximately two orders of magnitude when compared to neat PVA. Further, for composite hydrogels containing either 50 wt% UCL or CBL, no MB was detected in the receiving reservoir over the duration of the permeation experiment. In general, an increase in Young's moduli was observed in PVA–lignin hydrogels containing CBLs, where hydrogels composed of 50 wt% CBLs exhibited ∼40% increase when compared to neat PVA. In contrast, a ∼10% reduction in Young's moduli was observed for composite hydrogels containing 20 wt% UCLs or less, though these membranes exhibited the lowest MB permeabilities of all membranes investigated. However, the largest increase in membrane stiffness was observed for composite hydrogels containing 50 wt% UCLs, where a ∼70% increase in Young's modulus was observed. Finally, the concentration and functionalization of the lignins was seen to have a direct impact on the network structure of the soft composites, where in general, the molecular weight between crosslinks is seen to decrease with increasing lignin concentration.