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Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation

[Image: see text] Polymeric membranes are used on very large scales for drinking water production and kidney dialysis, but they are nearly always prepared by using large quantities of unsustainable and toxic aprotic solvents. In this study, a water-based, sustainable, and simple way of making polyme...

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Autores principales: Durmaz, Elif Nur, Baig, Muhammad Irshad, Willott, Joshua D., de Vos, Wiebe M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359294/
https://www.ncbi.nlm.nih.gov/pubmed/32685925
http://dx.doi.org/10.1021/acsapm.0c00255
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author Durmaz, Elif Nur
Baig, Muhammad Irshad
Willott, Joshua D.
de Vos, Wiebe M.
author_facet Durmaz, Elif Nur
Baig, Muhammad Irshad
Willott, Joshua D.
de Vos, Wiebe M.
author_sort Durmaz, Elif Nur
collection PubMed
description [Image: see text] Polymeric membranes are used on very large scales for drinking water production and kidney dialysis, but they are nearly always prepared by using large quantities of unsustainable and toxic aprotic solvents. In this study, a water-based, sustainable, and simple way of making polymeric membranes is presented without the need for harmful solvents or extreme pH conditions. Membranes were prepared from water-insoluble polyelectrolyte complexes (PECs) via aqueous phase separation (APS). Strong polyelectrolytes (PEs), poly(sodium 4-styrenesulfonate) (PSS), and poly(diallyldimethylammonium chloride) (PDADMAC) were mixed in the presence of excess of salt, thereby preventing complexation. Immersing a thin film of this mixture into a low-salinity bath induces complexation and consequently the precipitation of a solid PEC-based membrane. This approach leads to asymmetric nanofiltration membranes, with thin dense top layers and porous, macrovoid-free support layers. While the PSS molecular weight and the total polymer concentrations of the casting mixture did not significantly affect the membrane structure, they did affect the film formation process, the resulting mechanical stability of the films, and the membrane separation properties. The salt concentration of the coagulation bath has a large effect on membrane structure and allows for control over the thickness of the separation layer. The nanofiltration membranes prepared by APS have a low molecular weight cutoff (<300 Da), a high MgSO(4) retention (∼80%), and good stability even at high pressures (10 bar). PE complexation induced APS is a simple and sustainable way to prepare membranes where membrane structure and performance can be tuned with molecular weight, polymer concentration, and ionic strength.
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spelling pubmed-73592942020-07-15 Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation Durmaz, Elif Nur Baig, Muhammad Irshad Willott, Joshua D. de Vos, Wiebe M. ACS Appl Polym Mater [Image: see text] Polymeric membranes are used on very large scales for drinking water production and kidney dialysis, but they are nearly always prepared by using large quantities of unsustainable and toxic aprotic solvents. In this study, a water-based, sustainable, and simple way of making polymeric membranes is presented without the need for harmful solvents or extreme pH conditions. Membranes were prepared from water-insoluble polyelectrolyte complexes (PECs) via aqueous phase separation (APS). Strong polyelectrolytes (PEs), poly(sodium 4-styrenesulfonate) (PSS), and poly(diallyldimethylammonium chloride) (PDADMAC) were mixed in the presence of excess of salt, thereby preventing complexation. Immersing a thin film of this mixture into a low-salinity bath induces complexation and consequently the precipitation of a solid PEC-based membrane. This approach leads to asymmetric nanofiltration membranes, with thin dense top layers and porous, macrovoid-free support layers. While the PSS molecular weight and the total polymer concentrations of the casting mixture did not significantly affect the membrane structure, they did affect the film formation process, the resulting mechanical stability of the films, and the membrane separation properties. The salt concentration of the coagulation bath has a large effect on membrane structure and allows for control over the thickness of the separation layer. The nanofiltration membranes prepared by APS have a low molecular weight cutoff (<300 Da), a high MgSO(4) retention (∼80%), and good stability even at high pressures (10 bar). PE complexation induced APS is a simple and sustainable way to prepare membranes where membrane structure and performance can be tuned with molecular weight, polymer concentration, and ionic strength. American Chemical Society 2020-06-01 2020-07-10 /pmc/articles/PMC7359294/ /pubmed/32685925 http://dx.doi.org/10.1021/acsapm.0c00255 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Durmaz, Elif Nur
Baig, Muhammad Irshad
Willott, Joshua D.
de Vos, Wiebe M.
Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title_full Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title_fullStr Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title_full_unstemmed Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title_short Polyelectrolyte Complex Membranes via Salinity Change Induced Aqueous Phase Separation
title_sort polyelectrolyte complex membranes via salinity change induced aqueous phase separation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359294/
https://www.ncbi.nlm.nih.gov/pubmed/32685925
http://dx.doi.org/10.1021/acsapm.0c00255
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