Mixtures of ionic liquids as more efficient media for cellulose dissolution.

Carbohydr Polym

Faculty of Chemistry, Adam Mickiewicz University, ul Umultowska 89b, 61-614 Poznan, Poland; Poznan Science and Technology Park, Adam Mickiewicz University Foundation, ul. Rubiez 46, 61-612 Poznan, Poland. Electronic address:

Published: December 2017

The ability to dissolve cellulose, by using mixtures of ionic liquids, has been studied and compared with results obtained for the corresponding single ionic liquids. The ionic liquid mixtures tested were a 3:7mol/mol mixture of 1-ethyl-3-methylimidazolium chloride ([Cmim]Cl) and 1-ethyl-3-methylimidazolium acetate ([Cmim][OAc]), and the eutectic mixture (i.e., a 5.1:4.9mol/mol ratio) of [Cmim]Cl and 1-butyl-3-methylimidazolium chloride (Cmim]Cl). The amount of dissolved cellulose was investigated at three different temperatures (323, 348, and 373K) for each system. The greatest amount of dissolved cellulose was obtained for the [Cmim]Cl+[Cmim][OAc] mixture, at 373K, and it was 40g per 100g of solvent. Moreover, attempts were made to lower the viscosity of the resulting systems and improve the dissolution capacity by addition of dimethylsulfoxide (DMSO) as co-solvent. Results showed that addition of DMSO at 50mol% allows the dissolution of even greater amounts of cellulose (up to 43g per 100g of solvent). To the best of our knowledge, this is the largest ever reported amount of dissolved cellulose in ionic liquid media. Additionally, physical properties (density, surface tension, and viscosity) of the investigated ionic liquid mixtures were determined and compared with the values of the corresponding parent salts. The dissolved cellulose could be easily reconstituted from its solution in ionic liquid mixtures by addition of water. The regenerated cellulose was characterized by powder X-ray diffraction (pXRD), thermogravimetric analysis (TGA), and optical microscopy. The analyses confirmed the conversion of the crystal structure of cellulose from cellulose I to cellulose II during the dissolution and regeneration process.

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Source
http://dx.doi.org/10.1016/j.carbpol.2017.09.025DOI Listing

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