Polymeric membranes are a highly viable technology for wastewater treatment, water purification, and other filtration operations. Accordingly, flat membranes were developed from extruded nanocomposites of polyamide 6 (PA6) and carbon nanotubes (MWCNT), varying the filler content to 1, 3, and 5 parts per hundred resin (phr). The membranes were produced using the phase inversion process through the immersion–precipitation technique. In total, eight membrane compositions were developed with solvent/polymer ratios of 80/20 (weight %). Calcium chloride (CaCl₂) was used as a pore-forming agent at a content of 10 phr. Thus, the characterizations performed were: solution viscosity, FTIR, contact angle measurement, SEM, AFM, water permeability test, and water vapor permeation test. The results showed that the high viscosity of membranes, excessive gelation time, and higher MWCNT contents contributed to a decrease and/or absence of flow. Through SEM images and water flow measurements, the significant influence of CaCl₂ was observed in modifying the membrane morphology (more interconnected porous structures), ensuring the presence of flow. The AFM images also confirm this phenomenon through the increase in roughness. Water vapor transmission increased with higher MWCNT content. These results demonstrate that PA6 and MWCNT membranes were effective for water filtration, only in those where CaCl₂ was used, and for water vapor initially.

Poly(lactic acid) (PLA) is a renewable and biodegradable polymer that has attracted considerable attention for sustainable packaging applications. However, its inherent brittleness limits its use in flexible films. In this study, PLA/poly(vinyl alcohol) (PVA) blend films were prepared by a single-solvent-casting rout at PLA/PVA weight ratios of 80/20, 70/30, 60/40, and 50/50 to investigate the influence of composition on their thermal, chemical, morphological, mechanical, optical, and water vapor barrier properties. Increasing the PVA content progressively modified the molecular organization of the system, the crystallization ability of the PLA phase and promoting a more homogeneous phase distribution. These structural changes resulted in a transition from a brittle behavior to increasingly ductile films, with the PLA/PVA 50/50 composition exhibiting the most favorable combination of tensile toughness, transparency, and morphological homogeneity, reaching an elongation at break of approximately 60%. In contrast, the increase in the hydrophilic phase led to higher water vapor permeability, highlighting the trade-off between mechanical performance and moisture barrier properties. Overall, the results demonstrate that controlling the PLA/PVA ratio provides an effective strategy for tailoring the morphology and functional properties of solvent-cast PLA/PVA films, contributing to a better understanding of the composition–structure–property relationships in biopolymer blends.