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Cellulosic aerogels as ultra-lightweight materials. Part 2: Synthesis and properties 2<sup>nd</sup> ICC 2007, Tokyo, Japan, October 25–29, 2007
91
Citations
27
References
2008
Year
Materials ScienceHydrogelsChemical EngineeringBiomanufacturingUltra-lightweight MaterialsOctober 25–29EngineeringCellulose IiCellulosic AerogelsPolymer ScienceCellulose AggregationScco 2Carbon AerogelsHemicelluloseNanocelluloseHydrothermal Processing
Abstract Ultra-lightweight cellulose aerogels can be obtained in three steps: (1) preparation of a cellulose solution in molten N -methylmorpholine- N -oxide monohydrate (NMMO·H 2 O) at 110–120°C and casting of the viscous mass into moulds; (2) extraction of the solidified castings with ethanol to initiate cellulose aggregation and to remove NMMO·H 2 O so that the fragile, fine-porous texture of cellulose II is largely retained; and (3) drying of the lyogel using supercritical carbon dioxide (scCO 2 ). According to this approach, cellulosic aerogels were prepared from eight commercial cellulosic materials and pulps and analysed for selected chemical, physicochemical and mechanical parameters. The results reveal that all aerogels obtained from 3% cellulose containing NMMO·H 2 O melts had a largely uniform mesoporous structure with an average pore size of ∼9–12 nm, surface area of 190–310 m 2 g -1 , and specific density of 0.046–0.069 g cm -3 , but rather low mechanical stability expressed as compressive yield strain of 2.9–5.5%. All samples showed viscoelastic behaviour, with Young's modulus ranging from ∼5 to 10 N mm -2 . Doubling the cellulose content in the NMMO·H 2 O melt from 3% to 6% increased Young's modulus by one order of magnitude. Shrinkage of the fragile cellulose bodies during scCO 2 drying was still considerable and is subject to further investigations. Influencing parameters such as scCO 2 pressure, cellulose content, regenerating solvent and the number of regenerating baths were optimised.
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