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dc.contributor.authorOwens, Crystal E.
dc.contributor.authorDu, Jianyi
dc.contributor.authorSanchez Vazquez, Pablo Breogan 
dc.date.accessioned2022-12-02T11:10:03Z
dc.date.available2022-12-02T11:10:03Z
dc.date.issued2022-05-09
dc.identifier.citationBiomacromolecules, 23(5): 1958-1969 (2022)
dc.identifier.issn15257797
dc.identifier.issn15264602
dc.identifier.urihttp://hdl.handle.net/11093/4207
dc.descriptionFinanciado para publicación en acceso aberto: Universidade de Vigo/CISUG
dc.description.abstractIonic liquids (ILs) hold great potential as solvents to dissolve, recycle, and regenerate cellulosic fabrics, but the dissolved cellulose material system requires greater study in conditions relevant to fiber spinning processes, especially characterization of nonlinear shear and extensional flows. To address this gap, we aimed to disentangle the effects of the temperature, cellulose concentration, and degree of polymerization (DOP) on the shear and extensional flows of cellulose dissolved in an IL. We have studied the behavior of cellulose from two sources, fabric and filter paper, dissolved in 1-ethyl-3-methylimidazolium acetate ([C2C1Im][OAc]) over a range of temperatures (25 to 80 °C) and concentrations (up to 4%) that cover both semidilute and entangled regimes. The linear viscoelastic (LVE) response was measured using small-amplitude oscillatory shear techniques, and the results were unified by reducing the temperature, concentration, and DOP onto a single master curve using time superposition techniques. The shear rheological data were further fitted to a fractional Maxwell liquid (FML) model and were found to satisfy the Cox–Merz rule within the measurement range. Meanwhile, the material response in the non-LVE (NLVE) regime at large strains and strain rates has special relevance for spinning processes. We quantified the NLVE behavior using steady shear flow tests alongside uniaxial extension using a customized capillary breakup extensional rheometer. The results for both shear and extensional NLVE responses were described by the Rolie-Poly model to account for flow-dependent relaxation times and nonmonotonic viscosity evolution with strain rates in an extensional flow, which primarily arise from complex polymer interactions at high concentrations. The physically interpretable model fitting parameters were further compared to describe differences in material response to different flow types at varying temperatures, concentrations, and DOP. Finally, the fitting parameters from the FML and Rolie-Poly models were connected under the same superposition framework to provide a comprehensive description within the wide measured parameter window for the flow and handling of cellulose in [C2C1Im][OAc] in both linear and nonlinear regimes.
dc.description.sponsorshipXunta de Galicia | Ref. ED481B-2018/060
dc.language.isoeng
dc.publisherBiomacromolecules
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleUnderstanding the Dynamics of Cellulose Dissolved in an Ionic Liquid Solvent Under Shear and Extensional Flowsen
dc.typearticle
dc.rights.accessRightsopenAccess
dc.identifier.doi10.1021/acs.biomac.1c01623
dc.identifier.editorhttps://pubs.acs.org/doi/10.1021/acs.biomac.1c01623
dc.publisher.departamentoFísica aplicada
dc.publisher.grupoinvestigacionProcesos de Separación
dc.subject.unesco2307 Química Física
dc.date.updated2022-12-02T11:09:26Z
dc.computerCitationpub_title=Biomacromolecules|volume=23|journal_number=5|start_pag=1958|end_pag=1969


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    Except where otherwise noted, this item's license is described as Attribution 4.0 International