Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25591
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dc.contributor.authorHazer, Baki-
dc.contributor.authorBaysal, Bahattin M.-
dc.contributor.authorKoseoğlu, Ayşe G.-
dc.date.accessioned2022-04-06T07:08:01Z-
dc.date.available2022-04-06T07:08:01Z-
dc.date.issued2012-06-
dc.identifier.citationHazer, B. vd. (2012). "Synthesis of polylactide-b-poly (dimethyl siloxane) block copolymers and their blends with pure polylactide". Journal of Polymers and the Environment, 20(2), 477-484.en_US
dc.identifier.issn1566-2543-
dc.identifier.issn1572-8919-
dc.identifier.urihttps://doi.org/10.1007/s10924-011-0406-1-
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs10924-011-0406-1-
dc.identifier.urihttp://hdl.handle.net/11452/25591-
dc.description.abstractThe synthesis of polylactide (PLA)-b-poly (dimethyl siloxane) (PDMS) linear block copolymers and their use in blends with pure-PLA are described. PLA-b-PDMS linear block copolymers were obtained by the transesterification reaction in chloroform solution between poly(dimethyl siloxane) bis (2-aminopropyl ether) (molecular weight 2,000 Da) with PLA in the presence of stannous octoate. Molecular weights (Mw) of the block copolymers were varied from 53,800 to 63,600 Da while that of pristine PLA was 73,600 Da. The copolymers obtained were purified by fractional precipitation and then characterized by H-1 NMR, FTIR, GPC, viscometry and DSC techniques. Blends of pure PLA with PLA-b-PDMS block copolymers displayed improved elastic properties (elongation up to 140%) compared to pure PLA (elongation similar to 9%). Thermal, mechanical and morphological characterization of the blends were also conducted.en_US
dc.description.sponsorshipBülent Ecevit Üniversitesitr_TR
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEngineeringen_US
dc.subjectPolymer scienceen_US
dc.subjectPoly(lactide)en_US
dc.subjectTransesterificationen_US
dc.subjectPoly(dimethyl siloxane)en_US
dc.subjectBlock copolymeren_US
dc.subjectBlends of polymersen_US
dc.subjectRing-opening polymerizationen_US
dc.subjectEpsilon-caprolactoneen_US
dc.subjectMethyl-methacrylateen_US
dc.subjectRenewable resourcesen_US
dc.subjectTriblock copolymersen_US
dc.subjectGraft-copolymersen_US
dc.subjectL-lactideen_US
dc.subjectDegradationen_US
dc.subjectPoly(epsilon-caprolactone)en_US
dc.subjectCrystallizationen_US
dc.subjectChlorine compoundsen_US
dc.subjectMicrochannelsen_US
dc.subjectMolecular weighten_US
dc.subjectPolyestersen_US
dc.subjectChloroform solutionsen_US
dc.subjectElastic propertiesen_US
dc.subjectFractional precipitationen_US
dc.subjectLinear block copolymersen_US
dc.subjectMorphological characterizationen_US
dc.subjectPoly lactideen_US
dc.subjectPolydimethylsiloxane pdmsen_US
dc.subjectTransesterification reactionen_US
dc.subjectChemical analysisen_US
dc.subjectChloroformen_US
dc.subjectElastic propertyen_US
dc.subjectPolymeren_US
dc.subjectPrecipitation (chemistry)en_US
dc.subjectBlock copolymersen_US
dc.titleSynthesis of polylactide-b-poly (dimethyl siloxane) block copolymers and their blends with pure polylactideen_US
dc.typeArticleen_US
dc.identifier.wos000304147400026tr_TR
dc.identifier.scopus2-s2.0-84861191788tr_TR
dc.relation.tubitakTÜBİTAKtr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage477tr_TR
dc.identifier.endpage484tr_TR
dc.identifier.volume20tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalJournal of Polymers and the Environmenten_US
dc.contributor.buuauthorBeşirli, Necati-
dc.contributor.buuauthorTaşkın, Elif-
dc.relation.collaborationYurt içitr_TR
dc.subject.wosEngineering, environmentalen_US
dc.subject.wosPolymer scienceen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ2 (Polymer science)en_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid6507924888tr_TR
dc.contributor.scopusid54685203600tr_TR
dc.subject.scopusGraft Copolymers; Fractional Precipitation; Propargyl Chlorideen_US
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