In this work, we report the successful fabrication of CO₂-philic polymer composite membranes using a polyacrylonitrile-r-poly(ethylene glycol) methyl ether methacrylate (PAN-r-PEGMA) copolymer. The series of PAN-r-PEGMA copolymers with various amounts of PEG content was synthesized by free radical polymerization in presence of AIBN initiator and the obtained copolymers were used for the fabrication of composite membranes. The synthesized copolymers show high molecular weights in the range of 44⁻56 kDa. We were able to fabricate thin film composite (TFC) membranes by dip coating procedure using PAN-r-PEGMA copolymers and the porous PAN support membrane. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were applied to analyze the surface morphology of the composite membranes. The microscopy analysis reveals the formation of the defect free skin selective layer of PAN-r-PEGMA copolymer over the porous PAN support membrane. Selective layer thickness of the composite membranes was in the range of 1.32⁻1.42 μm. The resulting composite membrane has CO₂ a permeance of 1.37 × 10-1 m³/m²·h·bar and an ideal CO₂/N₂, selectivity of 65. The TFC membranes showed increasing ideal gas pair selectivities in the order CO₂/N₂ > CO₂/CH₄ > CO₂/H₂. In addition, the fabricated composite membranes were tested for long-term single gas permeation measurement and these membranes have remarkable stability, proving that they are good candidates for CO₂ separation.
Keywords: composite membranes; copolymer; gas separation; polyacrylonitrile; polyethylene glycol.