THE INFLUENCE OF PEG MOLECULAR WEIGHT ON MORPHOLOGIES AND PROPERTIES OF PVDF ASYMMETRIC MEMBRANES
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THE INFLUENCE OF PEG MOLECULAR WEIGHT ON MORPHOLOGIES AND PROPERTIES OF PVDF ASYMMETRIC MEMBRANES
Vol. 26, Issue 4, Pages: 405-414(2008)
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Published:20 July 2008
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Dan-ying Zuo a, You-yi Xu b, Wei-lin Xu a, et al. THE INFLUENCE OF PEG MOLECULAR WEIGHT ON MORPHOLOGIES AND PROPERTIES OF PVDF ASYMMETRIC MEMBRANES[J]. 2008, 26(4): 405-414.
DOI:
Dan-ying Zuo a, You-yi Xu b, Wei-lin Xu a, et al. THE INFLUENCE OF PEG MOLECULAR WEIGHT ON MORPHOLOGIES AND PROPERTIES OF PVDF ASYMMETRIC MEMBRANES[J]. 2008, 26(4): 405-414.DOI:
THE INFLUENCE OF PEG MOLECULAR WEIGHT ON MORPHOLOGIES AND PROPERTIES OF PVDF ASYMMETRIC MEMBRANES
The preparation and properties of asymmetric poly(vinyldiene fluoride) (PVDF) membranes are described in this study. Membranes were prepared from a casting solution of PVDF
N
N-dimethylacetamide (DMAc) solvent and water-soluble poly(ethylene glycol) (PEG) additives by immersing them in water as coagulant medium. Experiments showed that when PEG molecular weight increased
the changes in the resultant membranes’ morphologies and properties showed a transition point at PEG6000. This indicated that PEG with a relatively low molecular weight was used as a pore-forming agent to enhance pure water flux and reduce solute rejection of membranes
but PEG was used as a pore-reducing agent with a further increment of PEG molecular weight to result in pure water flux decreasing and solute rejection increasing. Finally
combined with the precipitation rates of different membrane-forming systems
the membrane formation mechanism describing PEG mobility was discussed extensively basing on the length changes of PEG molecular chains and the affinity between PEG and casting solution. The results offered a better understanding of effects of PEG additives on membrane structure and properties.
Abstract
The preparation and properties of asymmetric poly(vinyldiene fluoride) (PVDF) membranes are described in this study. Membranes were prepared from a casting solution of PVDF
N
N-dimethylacetamide (DMAc) solvent and water-soluble poly(ethylene glycol) (PEG) additives by immersing them in water as coagulant medium. Experiments showed that when PEG molecular weight increased
the changes in the resultant membranes’ morphologies and properties showed a transition point at PEG6000. This indicated that PEG with a relatively low molecular weight was used as a pore-forming agent to enhance pure water flux and reduce solute rejection of membranes
but PEG was used as a pore-reducing agent with a further increment of PEG molecular weight to result in pure water flux decreasing and solute rejection increasing. Finally
combined with the precipitation rates of different membrane-forming systems
the membrane formation mechanism describing PEG mobility was discussed extensively basing on the length changes of PEG molecular chains and the affinity between PEG and casting solution. The results offered a better understanding of effects of PEG additives on membrane structure and properties.
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