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dc.contributor.authorLei, Linfeng
dc.contributor.authorLindbråthen, Arne
dc.contributor.authorSandru, Marius
dc.contributor.authorGutierrez, Maria Teresa Guzman
dc.contributor.authorZhang, Xiangping
dc.contributor.authorHillestad, Magne
dc.contributor.authorHe, Xuezhong
dc.date.accessioned2020-11-26T14:08:27Z
dc.date.available2020-11-26T14:08:27Z
dc.date.created2018-09-01T11:30:48Z
dc.date.issued2018
dc.identifier.issn2073-4360
dc.identifier.urihttps://hdl.handle.net/11250/2689827
dc.description.abstractThe mixture of the ionic liquid 1-ethyl-3-methylimidazolium acetate (EmimAc) and dimethylsulfoxide (DMSO) was employed to dissolve microcrystalline cellulose (MCC). A 10 wt % cellulose dope solution was prepared for spinning cellulose hollow fibers (CHFs) under a mild temperature of 50 °C by a dry–wet spinning method. The defect-free CHFs were obtained with an average diameter and thickness of 270 and 38 µm, respectively. Both the XRD and FTIR characterization confirmed that a crystalline structure transition from cellulose I (MCC) to cellulose II (regenerated CHFs) occurred during the cellulose dissolution in ionic liquids and spinning processes. The thermogravimetric analysis (TGA) indicated that regenerated CHFs presented a similar pyrolysis behavior with deacetylated cellulose acetate during pyrolysis process. This study provided a suitable way to directly fabricate hollow fiber carbon membranes using cellulose hollow fiber precursors spun from cellulose/(EmimAc + DMSO)/H2O ternary system.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectviscosityen_US
dc.subjectspinningen_US
dc.subjecthollow fiberen_US
dc.subjectcelluloseen_US
dc.subjectionic liquidsen_US
dc.titleSpinning Cellulose Hollow Fibers Using 1-Ethyl-3-methylimidazolium Acetate–Dimethylsulfoxide Co-Solventen_US
dc.title.alternativeSpinning Cellulose Hollow Fibers Using 1-Ethyl-3-methylimidazolium Acetate–Dimethylsulfoxide Co-Solventen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en_US
dc.source.pagenumber11en_US
dc.source.volume10en_US
dc.source.journalPolymersen_US
dc.source.issue9en_US
dc.identifier.doi10.3390/polym10090972
dc.identifier.cristin1605995
dc.relation.projectNorges forskningsråd: 267615en_US
dc.source.articlenumber972en_US
cristin.unitcode7401,80,1,0
cristin.unitnameBioteknologi og nanomedisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal