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dc.contributor.authorMarques, D.
dc.contributor.authorVainio, U.
dc.contributor.authorChaparro, N.
dc.contributor.authorCalo, Victor
dc.contributor.authorBezahd, A.
dc.contributor.authorPitera, J.
dc.contributor.authorPeinemann, K.
dc.contributor.authorNunes, S.
dc.date.accessioned2017-03-24T11:53:14Z
dc.date.available2017-03-24T11:53:14Z
dc.date.created2017-03-23T06:59:54Z
dc.date.issued2013
dc.identifier.citationMarques, D. and Vainio, U. and Chaparro, N. and Calo, V. and Bezahd, A. and Pitera, J. and Peinemann, K. et al. 2013. Self-assembly in casting solutions of block copolymer membranes. Soft Matter. 9 (23): pp. 5557-5564.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/51431
dc.identifier.doi10.1039/c3sm27475f
dc.description.abstract

Membranes with exceptional pore regularity and high porosity were obtained from block copolymer solutions. We demonstrate by small-angle X-ray scattering that the order which gives rise to the pore morphology is already incipient in the casting solution. Hexagonal order was confirmed in PS-b-P4VP 175k-b-65k solutions in DMF/THF/dioxane with concentrations as high as 24 wt%, while lamellar structures were obtained in more concentrated solutions in DMF or DMF/dioxane. The change in order has been understood with the support of dissipative particle dynamic modeling. © 2013 The Royal Society of Chemistry.

dc.publisherRSC Publishing
dc.titleSelf-assembly in casting solutions of block copolymer membranes
dc.typeJournal Article
dcterms.source.volume9
dcterms.source.number23
dcterms.source.startPage5557
dcterms.source.endPage5564
dcterms.source.issn1744-683X
dcterms.source.titleSoft Matter
curtin.departmentDepartment of Applied Geology
curtin.accessStatusFulltext not available


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