Dual optimized sulfonated polyethersulfone and functionalized multiwall carbon tube based composites high fouling resistance membrane for protein separation

• Main Authors: Muhammad Irfan, Muhammad Irfan, Irfan, Masooma, Idris, Ani, Alsubaie, Abdullah Saad, Mahmoud, Khaled Hussein, Mohd. Yusof, Noordin, Akhtar, Naeem
• Format: Article
• Language: English
• Published: MDPI 2022
• Subjects: QC Physics; QD Chemistry
• Online Access: http://eprints.utm.my/103167/1/AniIdris2022_DualOptimizedSulfonatedPolyethersulfone.pdf; http://eprints.utm.my/103167/; http://dx.doi.org/10.3390/membranes12030329
• Institution: Universiti Teknologi Malaysia

Commercial grade sulfonated-Polyethersulfone (S-PES) and functionalized multiwall carbon nanotube (f-MWCNT)/polyvinylpyrrolidone (PVP) nanocomposites (NCs) were used to enhance and optimize the antifouling, protein resistance and protein separation properties of the S-PES ultrafiltration membranes. The polarities of sulfonic groups of S-PES, carbonyl carbon of pyrrolidone, hydroxyl and carboxyl groups of f-MWCNT in the membrane composition helped to strongly bind each other through hydrogen bonding, as shown by Fourier-transform infrared spectroscopy (FTIR). These binding forces greatly reduced the leaching of NCs and developed long finger-like projection, as confirmed by elution ratio and cross-sectional studies of the membranes via field emission scanning electron microscope (FESEM). The contact angle was reduced up to 48% more than pristine PES. Atomic force microscopy (AFM) was employed to study the various parameters of surface roughness with 3d diagrams, while grain analysis of membrane surface provided a quantitative estimation about volume, area, perimeter, length, radius and diameter. The NCs/S-PES enhanced the flux rate with an impressive (80–84%) flux recovery ratio and (58–62%) reversible resistance (Rr) value in situ, with 60% and 54.4% lesser dynamic and static protein adsorption. The best performing membrane were reported to remove 31.8%, 66.3%, 83.6% and 99.9% for lysozyme-(14.6 kDa), trypsin-(20 kDa), pepsin-(34.6 kDa) and bovine serum albumin (BSA-66 kDa), respectively.