Viscosity Modification of Polymerizable Bicontinuous Microemulsion by Controlled Radical Polymerization for Membrane Coating Applications

• Published in: Membranes (Basel) Vol. 10; no. 9; p. 246
• Main Authors: Gukelberger, Ephraim, Hitzel, Christian, Mancuso, Raffaella, Galiano, Francesco, Bruno, Mauro Daniel Luigi, Simonutti, Roberto, Gabriele, Bartolo, Figoli, Alberto, Hoinkis, Jan
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 21-09-2020; MDPI AG
• Subjects: controlled radical polymerization; membrane coating; polymerizable bicontinuous microemulsion; viscosity modification; wastewater treatment; controlled radical polymerization; viscosity modification; membrane coating; wastewater treatment; polymerizable bicontinuous microemulsion
• ISSN: 2077-0375; 2077-0375
• DOI: 10.3390/membranes10090246

Membrane modification is becoming ever more relevant for mitigating fouling phenomena within wastewater treatment applications. Past research included a novel low-fouling coating using polymerizable bicontinuous microemulsion (PBM) induced by UV-LED polymerization. This additional cover layer deteriorated the filtration capacity significantly, potentially due to the observed high pore intrusion of the liquid PBM prior to the casting process. Therefore, this work addressed an innovative experimental protocol for controlling the viscosity of polymerizable bicontinuous microemulsions (PBM) before casting on commercial ultrafiltration (UF) membranes. Prior to the coating procedure, the PBM viscosity modulation was carried out by controlled radical polymerization (CRP). The regulation was conducted by introducing the radical inhibitor 2,2,6,6-tetramethylpiperidine 1-oxyl after a certain time (CRP time). The ensuing controlled radical polymerized PBM (CRP-PBM) showed a higher viscosity than the original unpolymerized PBM, as confirmed by rheological measurements. Nevertheless, the resulting CRP-PBM-cast membranes had a lower permeability in water filtration experiments despite a higher viscosity and potentially lower pore intrusion. This result is due to different polymeric structures of the differently polymerized PBM, as confirmed by solid-state nuclear magnetic resonance (NMR) investigations. The findings can be useful for future developments in the membrane science field for production of specific membrane-coating layers for diverse applications.