2015-09-01

Controlled molecular reorientation enables strong cellulose fibers regenerated from ionic liquid solutions

Johan Sundberg, Valentina Guccini, Karl M.O. HÃ¥kansson, German Salazar-Alvarez, Guillermo Toriz, Paul Gatenholm

Polymer 75 (2015) 119-124.
DOI: 10.1016/j.polymer.2015.08.035

Highlights:
• Strong cellulose fibers spun from ionic liquid solution.
• Extrusion process simulated in silica based upon rheological measurements.
• Increased DO for fibers regenerated with ethanol stretched at high RH.
• Significant improvement of mechanical properties for re-oriented fibers.
• Mechanical properties comparable to commercially available fibers.

Abstract:
Cellulose is difficult to solubilize and undergoes thermal decomposition prior to melting. In recent years ionic liquids have been evaluated as solvents of cellulose. In the regeneration process the non-solvent governs the resulting material's crystallinity. Water adsorbs to amorphous cellulose, acts as plasticizer and lowers the Tg, hence the degree of crystallinity will affect the potential strain induced reorientation. We prepared regenerated cellulose fibers form ionic liquid using different non-solvents. The influence of shear forces upon cellulose chain alignment during extrusion was simulated in silica based upon rheological measurements. The regenerated fibers had different physical, morphological and mechanical properties. Molecular re-orientation in fibers induced by mechanical strain, at humidities above the Tg, resulted in much improved mechanical properties with the Young's modulus reaching 23.4 ± 0.8 GPa and the stress at break 504.6 ± 51.9 MPa, which is comparable to commercially available cellulose fibers.


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