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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorBILLES, Elise
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorONWUKAMIKE, Kelechukwu N.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorCOMA, Veronique
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorGRELIER, Stéphane
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorPERUCH, Frédéric
IDREF: 152900748
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2016
dc.identifier.issn0144-8617
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20169
dc.description.abstractEnCellulose oligomers are water-soluble, on the contrary to cellulose, which greatly increase their application range. In this study, cellulose oligomers were obtained from the acidic hydrolysis of cellulose with phosphoric acid. The global yield in water-soluble oligomers was around 23% with polymerization degree (DP) ranging from 1 to 12. The cellulose oligomers DP distribution was successfully reduced by differential solubilisation in methanol as one of the goals of this work was to avoid the use of a time-consuming full chromatographic separation. The methanol -soluble oligomers were mainly low DP (<= 3). The oligomers of higher molar mass, composed of 42% of cellotetraose and 36% of cellopentaose, were then functionalized and coupled with stearic acid through azide-alkyne click chemistry to obtain amphiphilic compounds. The self -assembly of these new bio-based compounds was finally investigated by dynamic light scattering (DLS) and transmission electron microscopy (TEM) and their critical micellar concentration (CMC) was found to be in the same range as alkylmaltosides and alkylglucosides. (C) 2016 Elsevier Ltd. All rights reserved.
dc.language.isoen
dc.publisherElsevier
dc.subject.enAcidic hydrolysis
dc.subject.enCellulose oligomers
dc.subject.enDifferential solubilisation
dc.subject.enClick chemistry
dc.subject.enSelf-assembly
dc.subject.enCRITICAL MICELLE CONCENTRATION
dc.subject.enCELLO-OLIGOSACCHARIDES
dc.subject.enBLOCK-COPOLYMERS
dc.subject.enPOLYMERIZATION
dc.subject.enACID
dc.subject.enCELLODEXTRINS
dc.subject.enSURFACTANTS
dc.subject.enHYDROLYSIS
dc.subject.en1
dc.subject.en2
dc.subject.en4-ORTHOPIVALATE
dc.subject.enMANUFACTURE
dc.title.enCellulose oligomers production and separation for the synthesis of new fully bio-based amphiphilic compounds
dc.typeArticle de revue
dc.identifier.doi10.1016/j.carbpol.2016.07.107
dc.subject.halChimie/Polymères
bordeaux.journalCarbohydrate Polymers
bordeaux.page121-128
bordeaux.volume154
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01394338
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01394338v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Carbohydrate%20Polymers&amp;rft.date=2016&amp;rft.volume=154&amp;rft.spage=121-128&amp;rft.epage=121-128&amp;rft.eissn=0144-8617&amp;rft.issn=0144-8617&amp;rft.au=BILLES,%20Elise&amp;ONWUKAMIKE,%20Kelechukwu%20N.&amp;COMA,%20Veronique&amp;GRELIER,%20St%C3%A9phane&amp;PERUCH,%20Fr%C3%A9d%C3%A9ric&amp;rft.genre=article


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