Halloysite nanotubes for regulating thermodynamics and kinetics of polysulfone/poly (ethylene-co-vinyl alcohol) membranes with enhanced permeability

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作者
Sania Kadanyo
Christine N. Matindi
Nozipho N. Gumbi
Derrick S. Dlamini
Yunxia Hu
Zhenyu Cui
Benqiao He
Bhekie B. Mamba
Jianxin Li
机构
[1] Tiangong University,State Key Laboratory of Separation Membranes and Membrane Processes, National Center for International Joint Research on Membrane Science and Technology
[2] Tiangong University,School of Materials Science and Engineering
[3] University of South Africa Science Campus,Institute for Nanotechnology and Water Sustainability, College of Science, Engineering and Technology
[4] University of California,undefined
[5] Los Angeles (UCLA),undefined
[6] Department of Civil & Environmental Engineering,undefined
[7] UCLA California NanoSystems Institute and UCLA Institute of the Environment & Sustainability,undefined
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摘要
Controlling membrane morphology is crucial to improving the mechanical strength (MS) and hydrophilicity of porous membranes. Here we report on the fabrication of mixed matrix membranes (MMMs) free of macrovoids via non-solvent-induced phase separation (NIPS). Hydrophilic Halloysite nanotubes (HNTs) and poly (ethylene-co-vinyl alcohol) (EVOH) were mixed with Hydrophobic polysulfone (PSF) in the presence of polyethylene glycol (PEG) to fabricate MMMs. The results showed the formation of PSF/EVOH-MMMs with a spongy structure when the content of HNTs varied from 0.06- 0.12 wt.%, owing to the formation of strong hydrogen bonds between PSF, EVOH, PEG, and HNTs, confirmed by molecular dynamics (MD) simulations. The MS of MMMs with 0.12 wt.% HNTs was increased 2.2-fold (up to 6.22 MPa), while the contact angle (CA) was lowest at 47.42 ± 1.9°. In addition, the water permeability increased by a factor of 1.7 up to 419 L m−2 h−1 bar−1. The rejection rates of MMMs (M12) for oil and BSA were >90% and >95%, respectively. While the MMMs had > 90% flux recovery for both oil and BSA. We predict that this study will provide a method for controlling dope thermodynamics, formation dynamics, and morphology of MMMs while maintaining promising properties for improved separation performance.
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