The aim of this work is to fabricate nanostructured membranes from polysulfone-based block copolymers through self-assembly and non-solvent induced phase separation. Block copolymers containing polysulfone are novel materials for this purpose providing better mechanical and thermal stability to membranes than polystyrene-based copolymers, which have been exclusively used now.
Firstly, we synthesized a triblock copolymer, poly(tert-butyl acrylate)-b-polsulfone-b-poly(tert-butyl acrylate) through polycondensation and reversible addition-fragmentation chain-transfer polymerization. The obtained membrane has a highly porous interconnected skin layer composed of elongated micelles with a flower-like arrangement, on top of the graded finger-like macrovoids. Membrane surface hydrolysis was carried out in a combination with metal complexation to obtain metal-chelated membranes. The copper-containing membrane showed improved antibacterial capability.
Secondly, a poly(acrylic acid)-b-polysulfone-b-poly(acrylic acid) triblock copolymer obtained by hydrolyzing poly(tert-butyl acrylate)-b-polsulfone-b-poly(tert-butyl acrylate) formed a thin film with cylindrical poly(acrylic acid) microdomains in polysulfone matrix through thermal annealing. A phase inversion membrane was prepared from the same polymer via self-assembly and chelation-assisted non-solvent induced phase separation. The spherical micelles pre-formed in a selective solvent mixture packed into an ordered lattice in aid of metal-poly(acrylic acid) complexation. The space between micelles was filled with poly(acrylic acid)-metal complexes acting as potential water channels. The silver0 nanoparticle-decorated membrane was obtained by surface reduction, having three distinct layers with different particle sizes. Other amphiphilic copolymers containing polysulfone and water-soluble segments such as poly(ethylene glycol) and poly(N-isopropylacrylamide) were also synthesized through coupling reaction and copper0-mediated reversible-deactivation radical polymerization.
Finally, phase inversion membranes were prepared from polytriazole-polysulfone random copolymers, which were obtained by “clicking” 1,2,3-triazole ring substituents bearing OH groups onto the polysulfone backbone via copperI-catalyzed azide-alkyne cycloaddition. The increased hydrophilicity of membranes imparted the higher water permeability and fouling resistance to the ultrafiltration membranes. Polytriazole-b-polysulfone-b-polytriazole triblock copolymer was synthesized by RAFT and post-polymerization click modification. Hydrogen bond-mediated self-assembly induced the formation of a nanostructured polytriazole-b-polysulfone-b-polytriazole / poly(acrylic acid)-b-polysulfone-b-poly(acrylic acid) blend membrane with a 1: 1 stoichiometric ratio of triazole and acid. String-like fused micelles with polytriazole/poly(acrylic acid) corona were present on the membrane surface, after immersion in a coagulation bath of copper2+ aqueous solution.
| Identifer | oai:union.ndltd.org:kaust.edu.sa/oai:repository.kaust.edu.sa:10754/611785 |
| Date | 05 1900 |
| Creators | Xie, Yihui |
| Contributors | Nunes, Suzana Pereira, Biological and Environmental Science and Engineering (BESE) Division, Hong, Pei-Ying, Hadjichristidis, Nikos, Haddleton, David |
| Source Sets | King Abdullah University of Science and Technology |
| Language | English |
| Detected Language | English |
| Type | Dissertation |
| Rights | 2017-06-06, At the time of archiving, the student author of this dissertation opted to temporarily restrict access to it. The full text of this dissertation became available to the public after the expiration of the embargo on 2017-06-06. |
Page generated in 0.0023 seconds