2014
DOI: 10.1039/c3gc42396d
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Transition of cellulose crystalline structure in biodegradable mixtures of renewably-sourced levulinate alkyl ammonium ionic liquids, γ-valerolactone and water

Abstract: Here we report the dissolution of cellulose in technical grade and renewably sourced-ILs.

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Cited by 53 publications
(46 citation statements)
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“…These observations are in line with previous studies in which cellulose was dissolved in ionic liquids. [54][55][56] RCNPs were produced from the regenerated cellulose using mechanical disintegration with a microuidizer. Aer a 1% suspension of the regenerated cellulose was passed through the chambers of the microuidizer, a highly transparent solution was obtained.…”
Section: Resultsmentioning
confidence: 99%
“…These observations are in line with previous studies in which cellulose was dissolved in ionic liquids. [54][55][56] RCNPs were produced from the regenerated cellulose using mechanical disintegration with a microuidizer. Aer a 1% suspension of the regenerated cellulose was passed through the chambers of the microuidizer, a highly transparent solution was obtained.…”
Section: Resultsmentioning
confidence: 99%
“…such as those employed by Ferlin et al 71 and Jérôme et al 72 can be shown to promote biodegradability. such as those employed by Ferlin et al 71 and Jérôme et al 72 can be shown to promote biodegradability.…”
Section: Anionsmentioning
confidence: 94%
“…72 Finally the amino diol and triol examples (161-167) 69 also have high levels of biodegradability (OECD 301F) when simple carboxylic acid anions such as acetate, propanoate, isopropanoate, butanoate and pentanoate feature. 72 Finally the amino diol and triol examples (161-167) 69 also have high levels of biodegradability (OECD 301F) when simple carboxylic acid anions such as acetate, propanoate, isopropanoate, butanoate and pentanoate feature.…”
Section: Anionsmentioning
confidence: 99%
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“…This is because of the increased inter-planar spacing (d-spacing) created due the presence of two water molecules per two chain unit cell of cellulose II hydrate [32,33]. The increased d-spacing is also due to the weakening of the hydrophobic bonds (van der Waals interaction) thereby increasing the hydrophilicity [20,32,34]. In contrast to cellulose I, cellulose II has its glucopyranose rings stacked with each other by hydrophobic interactions along the (1 -1 0) plane, thereby resulting in an increased density of hydroxyl groups on the surface leading to increased hydrophilicity [20].…”
Section: Figmentioning
confidence: 99%