Process for fibrillating lignocellulosic material, fibres and their use
A lignocellulose and fiber technology, which is applied in fiber raw material treatment, cellulose pulp post-treatment modification, raw material pretreatment, etc. Ease of reagent recovery, effect of reducing sulfur emissions
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Embodiment 1
[0079] Embodiment 1: Preparation of 1-methyl-3-methylimidazolium dimethyl phosphate ([mmim]Me 2 PO 4 )
[0080] A mixture of 1-methylimidazole (50ml, 0.519mol) was added to trimethylphosphate (60.7ml, 0.519mol) with stirring at 100°C over 4 hours. The solution was heated at 100°C for an additional 18 hours. through via 1 H NMR / CDCl 3 A sample was analyzed to determine completion of the reaction of the mixture. The mixture was rotary evaporated under high vacuum for 18 hours to give the product as a pale yellow oil (110ml). pass 1 H NMR analysis determined the product to be >99% pure.
Embodiment 2
[0081] Example 2: Preparation of 1-ethyl-3-methylimidazolium dimethylphosphate ([emim]Me 2 PO 4 )
[0082] A mixture of 1-ethylimidazole (50ml, 0.519mol) was added to trimethylphosphate (60.7ml, 0.519mol) over 4 hours at 120°C with stirring. The solution was heated at 120°C for an additional 18 hours. through via 1 H NMR / CDCl 3 A sample was analyzed to determine completion of the reaction of the mixture. The mixture was rotary evaporated under high vacuum for 18 hours to give the product as a pale yellow oil (110ml). pass 1 H NMR analysis determined the product to be >99% pure.
Embodiment 3
[0083] Example 3: Preparation of 1-ethyl-3-methylimidazolium methylhydrogen phosphonate ([emim]MeHPO 3 )
[0084] A mixture of 1-ethylimidazole (50ml, 0.519mol) was added to diethylphosphite (47.6ml, 0.519mol) over 4 hours at 140°C with stirring. The solution was heated at 140°C for an additional 18 hours. through via 1 H NMR / CDCl 3 A sample was analyzed to determine completion of the reaction of the mixture. The mixture was rotovaped under high vacuum for 18 hours to give the product as a light yellow oil (97ml), which was obtained by 1 H NMR analysis determined the product to be >99% pure.
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