Soft matter | 2021

Tuning the charge of polyelectrolyte complex membranes prepared via aqueous phase separation.

 
 
 
 

Abstract


In this work, polyelectrolyte mixing ratio is studied as a tuning parameter to control the charge, and thus the separation properties of polyelectrolyte complex (PEC) membranes prepared via Aqueous Phase Separation (APS). In this approach, various ratios of poly(sodium 4-styrenesulfonate) (PSS) and poly(diallyldimethylammonium chloride) (PDADMAC) are mixed at high salinity and the PEC-based membranes are then precipitated using low salinity coagulation baths. The monomeric ratio of PSS to PDADMAC is varied from 1.0\u2009:\u20090.8 through to 1.0\u2009:\u20091.2. Obtained membranes have an asymmetric structure and function as nanofiltration membranes with on average 1 L m-2 h-1 bar-1 pure water permeance and <400 Da molecular weight cut-off (MWCO); except for the 1.0\u2009:\u20091.2 membrane, where the water permeance was much higher (>20 L m-2 h-1 bar-1) with a similarly low MWCO. For the first time, we report the formation of both negatively and positively charged PSS-PDADMAC based APS membranes, as determined by both streaming potential and salt retention measurements. We hypothesize that the salt type used in the APS process plays a key role in the observed change in membrane charge. The point where the membrane charge transitions from negative to positive is found to be between the 1.0\u2009:\u20090.9 and 1.0\u2009:\u20091.0 PSS\u2009:\u2009PDADMAC ratios. The polyelectrolyte ratio not only affects membrane charge, but also their mechanical properties. The 1.0\u2009:\u20090.9 and 1.0\u2009:\u20091.0 membranes perform the best amongst the membranes prepared in this study since they have high salt retentions (up to 90% Na2SO4 and 75% MgCl2, respectively) and better mechanical stability. The higher permeance of the more charged, and thus more swollen, 1.0\u2009:\u20090.8 and 1.0\u2009:\u20091.2 membranes provide a relevant new direction for the development of APS-based PEC membranes.

Volume None
Pages None
DOI 10.1039/d1sm01199e
Language English
Journal Soft matter

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