Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3ra40807h
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dc.titleCellulose regeneration from a cellulose/ionic liquid mixture: The role of anti-solvents
dc.contributor.authorGupta, K.M.
dc.contributor.authorHu, Z.
dc.contributor.authorJiang, J.
dc.date.accessioned2014-10-09T06:44:29Z
dc.date.available2014-10-09T06:44:29Z
dc.date.issued2013-08-21
dc.identifier.citationGupta, K.M., Hu, Z., Jiang, J. (2013-08-21). Cellulose regeneration from a cellulose/ionic liquid mixture: The role of anti-solvents. RSC Advances 3 (31) : 12794-12801. ScholarBank@NUS Repository. https://doi.org/10.1039/c3ra40807h
dc.identifier.issn20462069
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/88630
dc.description.abstractA molecular simulation study is reported to investigate the role of anti-solvents (water, ethanol, and acetone) in cellulose regeneration from a cellulose/1-n-butyl-3-methylimidazolium acetate ([BMIM][Ac]) mixture. Structural analysis based on radial distribution functions reveals that the interaction of cellulose-[BMIM][Ac] decreases in the order acetone > ethanol > water, with cellulose-[Ac]- forming the smallest number of H-bonds in water. However, the interaction of cellulose-cellulose increases in the reverse order (acetone < ethanol < water), with the largest number of H-bonds between cellulose chains being observed in water. Among the three solvents, water is identified to be the most effective at breaking the cellulose-[Ac]- H-bonds and leading to the subsequent formation of cellulose-cellulose H-bonds. Furthermore, the dynamic analysis based on survival time-correlation functions and mean-squared displacements demonstrates that [Ac]- in water has the shortest residence time near cellulose and the highest mobility compared to [Ac]- in ethanol and acetone. This simulation study suggests that water outperforms ethanol and acetone for cellulose regeneration, and provides a microscopic insight into the mechanism of cellulose regeneration. © The Royal Society of Chemistry 2013.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3ra40807h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/c3ra40807h
dc.description.sourcetitleRSC Advances
dc.description.volume3
dc.description.issue31
dc.description.page12794-12801
dc.description.codenRSCAC
dc.identifier.isiut000321791200040
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