Dissolution and Hydrolysis of Bleached Kraft Pulp Using Ionic Liquids

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Journal Title
Journal ISSN
Volume Title
A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Date
2019-04-01
Major/Subject
Mcode
Degree programme
Language
en
Pages
16
Series
Polymers, Volume 11, issue 4
Abstract
Forestry industries in Chile are facing an important challenge—diversifying their products using green technologies. In this study, the potential use of Ionic Liquids (ILs) to dissolve and hydrolyze eucalyptus wood (mix of Eucalyptus nitens and Eucalyptus globulus) kraft pulp was studied. The Bleached Hardwood Kraft Pulp (BHKP) from a Chilean pulp mill was used together with five different ILs: 1-butyl-3-methylimidazolium chloride [bmim][Cl], 1-butyl-3-methylimidazolium acetate [bmim][Ac], 1-butyl-3-methylimidazolium hydrogen sulfate [bmim][HSO4], 1-ethyl-3-methylimidazolium chloride [emim][Cl], 1-ethyl-3-methylimidazolium acetate [emim][Ac]. Experimentally, one vacuum reactor was designed to study the dissolution/hydrolysis process for each ILs; particularly, the cellulose dissolution process using [bmim][Cl] was studied proposing one molecular dynamic model. Experimental characterization using Atomic Force Microscopy, conductometric titration, among other techniques suggest that all ILs are capable of cellulose dissolution at different levels; in some cases, the dissolution evolved to partial hydrolysis appearing cellulose nanocrystals (CNC) in the form of spherical aggregates with a diameter of 40–120 nm. Molecular dynamics simulations showed that the [bmim][Cl] anions tend to interact actively with cellulose sites and water molecules in the dissolution process. The results showed the potential of some ILs to dissolve/hydrolyze the cellulose from Chilean Eucalyptus, maintaining reactive forms.
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Keywords
Cellulose dissolution, Green technology, Ionic liquid, Nanocellulose
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Citation
Reyes, G, Graciela Aguayo, M, Perez, A F, Pääkkönen, T, Gacitua, W & Rojas, O J 2019, ' Dissolution and Hydrolysis of Bleached Kraft Pulp Using Ionic Liquids ', Polymers, vol. 11, no. 4, 673 . https://doi.org/10.3390/polym11040673