Co-Solvent Facilitated in situ Esterification of Cellulose in 1-Ethyl-3-Methylimidazolium Acetate
Artikel i vetenskaplig tidskrift, 2017

The homogeneous conversion of cellulose to cellulose propionate with propionic acid anhydride in the ionic liquid 1-ethyl-3-methylimidazolium acetate and two different co-solvents, dimethyl sulfoxide and 1methylimidazole, was studied. The software MODDE was used to generate an experimental design and evaluate the significance of the studied parameters. The methods 1H and 13C nuclear magnetic resonance (NMR) spectrometry and ion chromatography were used to analyze the obtained materials both qualitatively and quantitatively. The NMR spectrometry of dissolved cellulose esters confirmed there was covalent bonding with an even distribution pattern. From both ion chromatography and NMR spectroscopic data, it was concluded that by adding large amounts of co-solvent and using a high reagent-to-anhydroglucose unit ratio, it was possible to reduce the amount of acetylation caused by acetate anions in the ionic liquid. At the same time, it was shown that the reaction time and temperature was not at all significant in this respect. There was no notable difference detected in the degree of substitution between the reactions performed using dimethyl sulfoxide or 1methylimidazole as a co-solvent.

acetylation

ionic liquids

Design of Experiment

polysaccharides

Co-solvent

Cellulose derivatization

dimethyl sulfoxide/tetrabutylammonium fluoride

Esterification

Materials Science

acylation

Ionic liquid

Författare

Carina Olsson

Chalmers, Kemi och kemiteknik, Kemi och biokemi

Gunnar Westman

Chalmers, Kemi och kemiteknik, Kemi och biokemi

BioResources

1930-2126 (ISSN) 19302126 (eISSN)

Vol. 12 1 1395-1402

Drivkrafter

Hållbar utveckling

Ämneskategorier

Fysikalisk kemi

Biokemi och molekylärbiologi

Organisk kemi

Styrkeområden

Materialvetenskap

DOI

10.15376/biores.12.1.1395-1402

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Senast uppdaterat

2024-08-14