Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/90401
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dc.titleThree-dimensionally ordered porous membranes prepared via self-assembly and reverse micelle formation from well-defined amphiphilic block copolymers
dc.contributor.authorFu, G.D.
dc.contributor.authorKang, E.T.
dc.contributor.authorNeoh, K.G.
dc.date.accessioned2014-10-09T07:04:52Z
dc.date.available2014-10-09T07:04:52Z
dc.date.issued2005-04-12
dc.identifier.citationFu, G.D., Kang, E.T., Neoh, K.G. (2005-04-12). Three-dimensionally ordered porous membranes prepared via self-assembly and reverse micelle formation from well-defined amphiphilic block copolymers. Langmuir 21 (8) : 3619-3624. ScholarBank@NUS Repository.
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/90401
dc.description.abstractBlock copolymers of poly(pentafluorostyrene) (PFS) and poly(tert-butyl acrylate) (PtBA), or PFS-b-PtBA copolymers, were synthesized via consecutive atom transfer radical polymerizations (ATRPs). Amphiphilic block copolymers of PFS and poly(acrylic acid) (PFS-b-PAAC copolymers) were prepared via hydrolysis of the corresponding PFS-b-PtBA copolymers. The chemical structure and composition of the PFS-b-PtBA and PFS-b-PAAC block copolymers were studied by nuclear magnetic resonance (NMR) spectroscopy, themogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS). The amphiphilic PFS-b-PAAC copolymers were cast into porous membranes by phase inversion in aqueous media. The surface and cross-sectional morphology of the PFS-b-PAAC membranes were studied by scanning electron microscopy (SEM). Membranes with well-defined pores of sizes in the micrometer range were obtained as a result of inverse micelle formation. The pH of the aqueous media for phase inversion and the PAAC content in the PFS-b-PAAC copolymers could be used to adjust the pore size of the membranes. © 2005 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/la047619p
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.sourcetitleLangmuir
dc.description.volume21
dc.description.issue8
dc.description.page3619-3624
dc.description.codenLANGD
dc.identifier.isiut000228218700060
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