“…5) are in good agreement with the theoretical values derived using the [38]. Furthermore, oxygen relative permeability experiments [39] at 50% RH -oxygen permeation experiments on preequilibrated with water samples -exhibit a significant increase, although the value for composite film is much lower, than the corresponding of the pure polymeric one. This behavior can be attributed to the fact that water acts as plasticizer, increasing the polymer free volume and reducing the crystallinity of the polymeric chains [40].…”
“…5) are in good agreement with the theoretical values derived using the [38]. Furthermore, oxygen relative permeability experiments [39] at 50% RH -oxygen permeation experiments on preequilibrated with water samples -exhibit a significant increase, although the value for composite film is much lower, than the corresponding of the pure polymeric one. This behavior can be attributed to the fact that water acts as plasticizer, increasing the polymer free volume and reducing the crystallinity of the polymeric chains [40].…”
“…Small‐angle scattering is applied to characterize all types of materials at the nanometre scale in a typical interval of 1–200 nm. [ 52 ] This operational window gives access to a size‐scale regime below the macro to micrometre ones observed by SEM or mercury porosimetry. In general, four SANS and SAXS features can be observed in the experimental data plotted in Figure : i) the scattering arising from the nano‐inhomogeneities generated within the membranes due to the phase/domain structuration of the polymer itself (characteristic size ≈2–3 nm); ii) the interparticle space created due to the MOF particles agglomeration within the polymer (characteristic size ≈10–20 nm); iii) the power law decay of the scattering data that is related to the aggregates with mass or surface fractal structures in the composites; and iv) the diffraction peak in the large q region due to the crystal structure of the MOF (similar peak was observed in our recent study of separators based on polymer composites with MOFs for battery [ 36 ] ).…”
Poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVDF‐HFP) is a highly versatile polymer used for water remediation due to its chemical robustness and processability. By incorporating metal‐organic frameworks (MOFs) into PVDF‐HFP membranes, the material can gain metal‐adsorption properties. It is well known that the effectiveness of these composites removing heavy metals depends on the MOF's chemical encoding and the extent of encapsulation within the polymer. In this study, it is examined how the micro to nanoscale structure of PVDF‐HFP@MOF membranes influences their adsorption performance for CrVI. To this end, the micro‐ and nanostructure of PVDF‐HFP@MOF membranes are thoroughly studied by a set of complementary techniques. In particular, small‐angle X‐ray and neutron scattering allow to precisely describe the nanostructure of the polymer‐MOF complex systems, while scanning microscopy and mercury porosimetry give a clear insight into the macro and mesoporosity of the system. By correlating nanoscale structural features with the adsorption capacity of the MOF nanoparticles, different degrees of full encapsulation‐based on the PVDF‐HFP processing and structuration from the macro to nanometer scale are observed. Additionally, the in situ functionalization of MOF nanoparticles with cysteine is investigated to enhance their adsorption toward HgII. This functionalization enhanced the adsorption capacity of the MOFs from 8 to 30 mg·g−1.
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