Toward Predicting the Formation of Integral-Asymmetric, Isoporous Diblock Copolymer Membranes

© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2024) vom: 29. Aug., Seite e2404560
1. Verfasser: Blagojevic, Niklas (VerfasserIn)
Weitere Verfasser: Das, Shibananda, Xie, Jiayu, Dreyer, Oliver, Radjabian, Maryam, Held, Martin, Abetz, Volker, Müller, Marcus
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article block copolymer membranes evaporation‐induced self‐assembly (EISA) molecular modeling nonsolvent‐induced phase separation (NIPS)
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520 |a The self-assembly and nonsolvent-induced phase separation (SNIPS) process of block copolymers and solvents enables the fabrication of integral-asymmetric, isoporous membranes. An isoporous top layer is formed by evaporation-induced self-assembly (EISA) and imparts selectivity for ultrafiltration of functional macromolecules or water purification. This selective layer is supported by a macroporous bottom structure that is formed by nonsolvent-induced phase separation (NIPS) providing mechanical stability. Thereby the permeability/selectivity tradeoff is optimized. The SNIPS fabrication involves various physical phenomena-e.g., evaporation, self-assembly, macrophase separation, vitrification - and multiple structural, thermodynamic, kinetic, and process parameters. Optimizing membrane properties and rationally designing fabrication processes is a challenge which particle simulation can significantly contribute to. Using large-scale particle simulations, it is observed that 1) a small incompatibility between matrix-forming block of the copolymer and nonsolvent, 2) a glassy arrest that occurs at a smaller polymer concentration, or 3) a higher dynamical contrast between polymer and solvent results in a finer, spongy substructure, whereas the opposite parameter choice gives rise to larger macropores with an elongated shape. These observations are confirmed by comparison to experiments on polystyrene (PS)-block-poly(4-vinylpyridine) (P4VP) diblock copolymer membranes, varying the chemical nature of the coagulant or the temperature of coagulation bath 
650 4 |a Journal Article 
650 4 |a block copolymer membranes 
650 4 |a evaporation‐induced self‐assembly (EISA) 
650 4 |a molecular modeling 
650 4 |a nonsolvent‐induced phase separation (NIPS) 
700 1 |a Das, Shibananda  |e verfasserin  |4 aut 
700 1 |a Xie, Jiayu  |e verfasserin  |4 aut 
700 1 |a Dreyer, Oliver  |e verfasserin  |4 aut 
700 1 |a Radjabian, Maryam  |e verfasserin  |4 aut 
700 1 |a Held, Martin  |e verfasserin  |4 aut 
700 1 |a Abetz, Volker  |e verfasserin  |4 aut 
700 1 |a Müller, Marcus  |e verfasserin  |4 aut 
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773 1 8 |g year:2024  |g day:29  |g month:08  |g pages:e2404560 
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