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hal.structure.identifierInstitut Européen des membranes [IEM]
dc.contributor.authorAISSOU, Karim
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorMUMTAZ, Muhammad
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorBOUZIT, Hana
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorPÉCASTAINGS, Gilles
hal.structure.identifierUniv Groningen, Zernike Inst Adv Mat, Macromol Chem & New Polym Mat
dc.contributor.authorPORTALE, Giuseppe
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorFLEURY, Guillaume
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorHADZIIOANNOU, Georges
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2019
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19842
dc.description.abstractEnAsymmetric poly(1,1-dimethyl silacyclobutane)-block-polystyrene-block-poly(2-vinyl pyridine) (PDMSB-b-PS-b-P2VP) thick films, consisting of a spongelike substructure topped by a nanostructured dense top layer, were produced by combining a fast self-assembly of the triblock terpolymer chains with nonsolvent-induced phase separation (referred as SNIPS). A controlled evolution of the thickness and morphology of the nanostructured top layer was achieved upon solvent vapor annealing (SVA). For instance, the sub-100 nm thick square array morphology generated by SNIPS is transformed into a 1.5 mu m thick core-shell perforated lamellar (PL) structure when exposed to a chloroform (CHCl3) vapor for 3 h. A PL phase having highly ordered continuous P2VP nanochannels can be envisioned as an appealing morphology for membrane applications, since such a network structure formed on asymmetric PDMSB-b-PS-b-P2VP thick films obviates the need for alignment. Monoliths entirely composed of the bicontinuous PL structure were also produced by increasing the duration of the SVA treatment (18 h, CHCl3)
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enBLOCK-COPOLYMER MEMBRANES
dc.subject.enARCHIMEDEAN TILINGS
dc.subject.enMORPHOLOGY
dc.subject.enPHASE
dc.subject.enULTRAFILTRATION
dc.subject.enLAMELLAE
dc.subject.enARRAYS
dc.title.enBicontinuous Network Nanostructure with Tunable Thickness Formed on Asymmetric Triblock Terpolymer Thick Films
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.macromol.9b00572
dc.subject.halChimie
bordeaux.journalMacromolecules
bordeaux.page4413-4420
bordeaux.volume52
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue12
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-02199632
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02199632v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecules&rft.date=2019&rft.volume=52&rft.issue=12&rft.spage=4413-4420&rft.epage=4413-4420&rft.eissn=0024-9297&rft.issn=0024-9297&rft.au=AISSOU,%20Karim&MUMTAZ,%20Muhammad&BOUZIT,%20Hana&P%C3%89CASTAINGS,%20Gilles&PORTALE,%20Giuseppe&rft.genre=article


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