Hydrophilic polyvinyl alcohol coating on hydrophobic electrospun nanofiber membrane for high performance thin film composite forward osmosis membrane

被引:163
|
作者
Park, Myoung Jun [1 ]
Gonzales, Ralph Rolly [1 ]
Abdel-Wahab, Ahmed [2 ]
Phuntsho, Sherub [1 ]
Shon, Ho Kyong [1 ]
机构
[1] Univ Technol Sydney, Sch Civil & Environm Engn, Ctr Technol Water & Wastewater, POB 123,15 Broadway, Sydney, NSW 2007, Australia
[2] Texas A&M Univ Qatar, Chem Engn Program, POB 23874, Doha, Qatar
基金
澳大利亚研究理事会;
关键词
Forward osmosis; Electrospinning; Nanofiber membrane; Polyvinylidene fluoride; Polyvinyl alcohol; INTERNAL CONCENTRATION POLARIZATION; SULFONATED POLYPHENYLENESULFONE SPPSU; PRESSURE RETARDED OSMOSIS; MICROFILTRATION MEMBRANE; WATER; SUPPORT; NANOCOMPOSITE; SUBSTRATE; LAYER; DESALINATION;
D O I
10.1016/j.desal.2017.10.042
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, the hydrophilic property of polyvinyl alcohol (PVA) was utilized to improve the hydrophilicity and mechanical strength of electrospun polyvinylidene fluoride (PVDF)-supported thin film composite (TFC) forward osmosis (FO) membranes. The PVDF nanofiber support was modified with PVA via dip coating and acid-catalyzed crosslinking with glutaraldehyde prior to formation of polyamide active layer on the support via interfacial polymerization. The influence of PVA modification on the morphology and physical properties of PVDF support was evaluated through several characterization techniques while the flux performance was assessed using lab scale FO membrane unit. The fabricated PVA-modified TFC FO membranes exhibited high hydrophilicity, porosity, and mechanical strength. FO performance tests reveal excellent flux performance (34.2 LMH using 1 M NaCl and DI water as draw and feed solution, respectively) and low structural parameters (154 pm) of the PVA-modified TFC FO membrane. Dip coating of the nanofiber support in PVA is therefore a simple and effective method for the improvement of PVDF support hydrophilicity to fabricate high performance TFC FO membranes.
引用
收藏
页码:50 / 59
页数:10
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