Damages to water filtration membranes during installation and operation are known to cause detrimental loss of the product water quality. Membranes that have the ability to self-heal would recover their original rejection levels autonomously, bypassing the need for costly integrity monitoring and membrane replacement practices. Herein, we fabricated hydrogel pore-filled membranes via in situ graft polymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) onto microporous poly(ether sulfone) (PES) substrates and successfully demonstrated their self-healing ability. Covalent attachment of the hydrogel to the substrate was essential for stable membrane performance. The membranes autonomously restore their particle rejection up to 99% from rejection levels as low as 30% after being physically damaged. We attribute the observed self-healing property to swelling of the pore-filling hydrogel into the damage site, strong hydrogen bonding, and molecular interdiffusion. The results of this study show that hydrogel pore-filled membranes are a promising new class of materials for fabricating self-healing membranes.
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http://dx.doi.org/10.1021/acs.est.6b04574 | DOI Listing |
Membranes (Basel)
March 2023
School of Polymer Science and Polymer Engineering, The University of Akron, Akron, OH 44325, USA.
A 248 nm KrF excimer laser can be used to manufacture temperature and pH-responsive polymer-based membranes for controlled transport applications. This is done by a two-step approach. In the first step, well-defined/shaped and orderly pores are created on commercially available polymer films by ablation by using an excimer laser.
View Article and Find Full Text PDFChemosphere
January 2023
College of Biological and Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou, 310023, China. Electronic address:
In this work, the self-healing polyethersulfone ultrafiltration membrane constructed by host-guest chemistry between cucurbit [8]uril (CB [8] is a family of macrocyclic compounds comprising 8 glycoluril units) and two guest molecules based on reverse thermally induced phase separation (RTIPS) method was developed, which had excellent self-healing performance, better mechanical properties, and high permeation flux and BSA rejection rate. The membrane autonomously restored it BSA rejection rate up to about 89% from rejection rate levels as low as 21% after damage. The observed self-healing performance were attributed to the swelling of pore-filled CB [8] hydrogel into the damage position, the molecular interdiffusion of the hydrogel chains, the strong hydrogen bond of the hydrogel chains and the host-guest interaction between CB [8] and two guest molecules (HEC-Np and PVA-MV).
View Article and Find Full Text PDFEnviron Sci Technol
January 2017
Department of Chemical and Environmental Engineering, Yale University, New Haven, Connecticut 06511, United States.
Damages to water filtration membranes during installation and operation are known to cause detrimental loss of the product water quality. Membranes that have the ability to self-heal would recover their original rejection levels autonomously, bypassing the need for costly integrity monitoring and membrane replacement practices. Herein, we fabricated hydrogel pore-filled membranes via in situ graft polymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) onto microporous poly(ether sulfone) (PES) substrates and successfully demonstrated their self-healing ability.
View Article and Find Full Text PDFJ Mater Chem B
February 2016
Lehrstuhl für Technische Chemie II, Universität Duisburg-Essen, 45117 Essen, Germany.
Stimuli-responsive separation membranes with tunable molecular scale pore size, which are desirable for on-demand sieving of targeted macromolecules, have attracted increasing attention in recent years. In this study, novel magneto-hydrogel pore-filled composite membranes with excellent magneto-responsivity and tunability for molecular sieving have been developed. Such membranes comprising magnetic nanoparticles (MNPs) as localized heater which can be excited by high frequency alternating magnetic field (AMF), poly(N-isopropylacrylamide) (PNIPAAm) hydrogel network as the sieving medium and actuator, and polyethylene terephthalate (PET) track-etched membrane as robust support, have been prepared via in situ reactive pore-filling functionalization.
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