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A versatile method for the surface tailoring of cellulose nanocrystal building blocks by acylation with functional vinyl esters

Authors :
Gilles Sèbe
Gilles Pecastaings
Jérémie Brand
Laboratoire de Chimie des Polymères Organiques (LCPO)
Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC)
Team 2 LCPO : Biopolymers & Bio-sourced Polymers
Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC)
Source :
Carbohydrate Polymers, Carbohydrate Polymers, Elsevier, 2017, 169, pp.189-197. ⟨10.1016/j.carbpol.2017.03.077⟩
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Herein we propose a versatile method for the surface tailoring of cellulose nanocrystals (CNCs) based on the reactivity of vinyl ester molecules toward the accessible hydroxyl groups located at the surface of the nanoparticles. CNCs produced from wood pulp were acylated in various conditions, with potassium carbonate as catalyst and under microwave activation. The impact of solvent, temperature and reagent concentration on the reaction efficiency and kinetics was then investigated, using vinyl acetate as a model vinyl ester. Results indicated that the chemical reactivity was significantly influenced by the quality of the CNCs dispersion in the solvent of reaction, the ratio of reagent relative to the CNCs surface OH groups, the diffusion of reagent and catalyst within the CNCs aggregates, and the different nucleophilic strengths of the surface hydroxyl groups. The versatility of the method was verified by extending the reaction to a selection of vinyl esters bearing various functionalities.

Details

ISSN :
01448617
Volume :
169
Database :
OpenAIRE
Journal :
Carbohydrate Polymers
Accession number :
edsair.doi.dedup.....67738f318d44771e7af9f7007ace17e2
Full Text :
https://doi.org/10.1016/j.carbpol.2017.03.077