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dc.contributor.authorHe, Xuezhong
dc.date.accessioned2018-06-07T09:15:37Z
dc.date.available2018-06-07T09:15:37Z
dc.date.created2017-06-29T23:46:14Z
dc.date.issued2017
dc.identifier.citationInternational Journal of Polymer Science. 2017, 2017 .nb_NO
dc.identifier.issn1687-9422
dc.identifier.urihttp://hdl.handle.net/11250/2500751
dc.description.abstractCellulose acetate (CA) hollow fibers were spun from a CA+ Polyvinylpyrrolidone (PVP)/N-methyl-2-pyrrolidone (NMP)/H2O dope solution and regenerated by deacetylation. The complete deacetylation time of 0.5 h was found at a high concentration (0.2 M) NaOH ethanol (96%) solution. The reaction rate of deacetylation with 0.5 M NaOH was faster in a 50% ethanol compared to a 96 vol.% ethanol. The hydrogen bond between CA and tertiary amide group of PVP was confirmed. The deacetylation parameters of NaOH concentration, reaction time, swelling time, and solution were investigated by orthogonal experimental design (OED) method. The degree of cross-linking, the residual acetyl content, and the PVP content in the deacetylated membranes were determined by FTIR analysis. The conjoint analysis in the Statistical Product and Service Solutions (SPSS) software was used to analyze the OED results, and the importance of the deacetylation parameters was sorted as Solution > Swelling time > Reaction time > Concentration. The optimal deacetylation condition of 96 vol.% ethanol solution, swelling time 24 h, the concentration of NaOH (0.075 M), and the reaction time (2 h) were identified. The regenerated cellulose hollow fibers under the optimal deacetylation condition can be further used as precursors for preparation of hollow fiber carbon membranes.nb_NO
dc.language.isoengnb_NO
dc.publisherHindawinb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleOptimization of Deacetylation Process for Regenerated Cellulose Hollow Fiber Membranesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber8nb_NO
dc.source.volume2017nb_NO
dc.source.journalInternational Journal of Polymer Sciencenb_NO
dc.identifier.doi10.1155/2017/3125413
dc.identifier.cristin1480001
dc.description.localcode© 2017 Xuezhong He. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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