1999
DOI: 10.1023/a:1009208417954
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Cited by 83 publications
(28 citation statements)
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“…But the as-prepared samples (CA-1, CA-2) become insoluble in DMSO when the reaction times are decreased from 0.5 h to 0.17 h (10 min) and 0.08 h (5 min). It can be seen that the three hydroxyl groups at C2, C3, and C6 position exhibit different reaction activities, and the order of reactivity is C6-OH > C2-OH > C3-OH, which is similar to the acetylation of cellulose in LiCl-1,3-dimethyl-2-50 imidazolidinone (DMI) solutions 33 and CO 2 -based reversible ionic liquids. The reaction temperature has significant effect on the reaction, which was evidenced by the fact that a product with DS of 2.26 (CA-9) was obtained when the reaction was performed at 50 o C in 5 h. CA with various DS were 15 also obtained through modifying the molar ratio of acetic anhydride/AGU.…”
mentioning
confidence: 86%
“…But the as-prepared samples (CA-1, CA-2) become insoluble in DMSO when the reaction times are decreased from 0.5 h to 0.17 h (10 min) and 0.08 h (5 min). It can be seen that the three hydroxyl groups at C2, C3, and C6 position exhibit different reaction activities, and the order of reactivity is C6-OH > C2-OH > C3-OH, which is similar to the acetylation of cellulose in LiCl-1,3-dimethyl-2-50 imidazolidinone (DMI) solutions 33 and CO 2 -based reversible ionic liquids. The reaction temperature has significant effect on the reaction, which was evidenced by the fact that a product with DS of 2.26 (CA-9) was obtained when the reaction was performed at 50 o C in 5 h. CA with various DS were 15 also obtained through modifying the molar ratio of acetic anhydride/AGU.…”
mentioning
confidence: 86%
“…Cellulose chemical modifications occur more easily in amorphous regions than in crystalline ones [2]. Homogeneous derivatization needs either activation [3] or solubilization [4][5][6][7][8][9][10][11][12][13][14][15] of the polymer before its modification [16,17].…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, there is great interest in the design of new dissolution technologies to allow homogeneous processing and derivatisation of cellulose towards a controllable facile preparation of cellulosic materials. To date, a rather limited number of solvents are available, such as cuprammonium hydroxide solution, monohydrate of N‐methyl‐N‐morpholine oxide (lyocell process), CS 2 –NaOH aqueous solution (viscose process), LiCl‐based solvents, ionic liquids, and NaOH–urea–water aqueous solution, organic bases/DMSO/CO 2 reversible system . It is well‐recognized that significant progress in cellulose dissolution technologies will promote the design and synthesis of new cellulosic materials.…”
Section: Figurementioning
confidence: 99%