Deformation mechanisms in ionic liquid spun cellulose fibers

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dc.contributor Aalto-yliopisto fi
dc.contributor Aalto University en
dc.contributor.author Wanasekara, Nandula D.
dc.contributor.author Michud, Anne
dc.contributor.author Zhu, Chenchen
dc.contributor.author Rahatekar, Sameer
dc.contributor.author Sixta, Herbert
dc.contributor.author Eichhorn, Stephen J.
dc.date.accessioned 2017-04-20T10:17:20Z
dc.date.available 2017-04-20T10:17:20Z
dc.date.issued 2016-09-02
dc.identifier.citation Wanasekara , N D , Michud , A , Zhu , C , Rahatekar , S , Sixta , H & Eichhorn , S J 2016 , ' Deformation mechanisms in ionic liquid spun cellulose fibers ' POLYMER , vol 99 , pp. 222-230 . DOI: 10.1016/j.polymer.2016.07.007 en
dc.identifier.issn 0032-3861
dc.identifier.issn 1873-2291
dc.identifier.other PURE UUID: 22c6593d-2d9d-4e3b-91e5-978ffe987f66
dc.identifier.other PURE ITEMURL: https://research.aalto.fi/en/publications/deformation-mechanisms-in-ionic-liquid-spun-cellulose-fibers(22c6593d-2d9d-4e3b-91e5-978ffe987f66).html
dc.identifier.other PURE LINK: http://www.scopus.com/inward/record.url?scp=84978198844&partnerID=8YFLogxK
dc.identifier.other PURE FILEURL: https://research.aalto.fi/files/11454632/Wanasekara_et_al_2016_Deformation_mechanisms.pdf
dc.identifier.uri https://aaltodoc.aalto.fi/handle/123456789/25223
dc.description.abstract The molecular deformation and crystal orientation of a range of next generation regenerated cellulose fibers, produced from an ionic liquid solvent spinning system, are correlated with macroscopic fiber properties. Fibers are drawn at the spinning stage to increase both molecular and crystal orientation in order to achieve a high tensile strength and Young's modulus for potential use in engineering applications. Raman spectroscopy was utilized to quantify both molecular strain and orientation of fibers deformed in tension. X-ray diffraction was used to characterize crystal orientation of single fibers. These techniques are shown to provide complimentary information on the microstructure of the fibers. A shift in the position of a characteristic Raman band, initially located at ∼1095 cm−1, emanating from the backbone structure of the cellulose polymer chains was followed under tensile deformation. It is shown that the shift rate of this band with respect to strain increases with the draw ratio of the fibers, indicative of an increase in the axial molecular alignment and subsequent deformation of the cellulose chains. A linear relationship between the Raman band shift rate and the modulus was established, indicating that the fibers possess a series aggregate structure of aligned crystalline and amorphous domains. Wide-angle X-ray diffraction data show that crystal orientation increases with an increase in the draw ratio, and a crystalline chain slip model was used to fit the change in orientation with fiber draw ratio. In addition to this a new model is proposed for a series aggregate structure that takes into better account the molecular deformation of the fibers. Using this model a prediction for the crystal modulus of a cellulose-II structure is made (83 GPa) which is shown to be in good agreement with other experimental approaches for its determination. en
dc.format.extent 9
dc.format.extent 222-230
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries POLYMER en
dc.relation.ispartofseries Volume 99 en
dc.rights openAccess en
dc.subject.other Organic Chemistry en
dc.subject.other Polymers and Plastics en
dc.subject.other 216 Materials engineering en
dc.title Deformation mechanisms in ionic liquid spun cellulose fibers en
dc.type A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä fi
dc.description.version Peer reviewed en
dc.contributor.department University of Exeter
dc.contributor.department Department of Forest Products Technology
dc.contributor.department University of Bristol
dc.contributor.department Department of Bioproducts and Biosystems en
dc.subject.keyword Cellulose
dc.subject.keyword Fibers
dc.subject.keyword Molecular deformation
dc.subject.keyword Organic Chemistry
dc.subject.keyword Polymers and Plastics
dc.subject.keyword 216 Materials engineering
dc.identifier.urn URN:NBN:fi:aalto-201704203653
dc.identifier.doi 10.1016/j.polymer.2016.07.007
dc.type.version publishedVersion


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