1979
DOI: 10.1016/s0008-6215(00)86085-1
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Some N-arylidenechitosan gels

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Cited by 45 publications
(9 citation statements)
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“…20 The proper amount of aldehyde was chosen from our previous work. 13 The gels, in which enzyme proteins were immobilized by the present method, were slightly yellow and were insoluble in cold and boiling water, aqueous alkali, and the common organic solvents examined. The gels did not melt on heating up to 200°C.…”
Section: Resultsmentioning
confidence: 89%
“…20 The proper amount of aldehyde was chosen from our previous work. 13 The gels, in which enzyme proteins were immobilized by the present method, were slightly yellow and were insoluble in cold and boiling water, aqueous alkali, and the common organic solvents examined. The gels did not melt on heating up to 200°C.…”
Section: Resultsmentioning
confidence: 89%
“…This is presumably a result of the relatively short experimental time scale involved (minutes) which would be insufficient for any substantial chclation to occur (23 ( 1 8) and other selective derivatization (6, 9) procedures for chitin and chitosan, which together provide a versatile array of synthetic techniques for further evaluations of the physical properties of these biopolyniers. These methods have facilitated, for the first time, spectroscopic studies of chitosan and its derivatives in both the solution and gel form in aquco~ls medium, whereas previous investigations involved either chitosan films suspended in organic solvents (4) or solutions in aqueous organic acids (3,5).…”
Section: Discussionmentioning
confidence: 99%
“…Hirano et 01. (3) have observed pronounced changes in specific rotation of chitosan during Schiff's base formation and the attendant gelation process. More recently, Komai and co-workers (4) have studied the molecular motions of a spin-probe in films of various acylchitins, while Aleksandrova et 01.…”
Section: Introductionmentioning
confidence: 99%
“…16 After chitosan flakes were broken into smaller pieces, chitosan particles with a diameter of 100 -300 µm were collected with a sieve. After amino groups of the chitosan were protected by benzaldehyde, 18 the hydroxyl groups at the 6-position of chitosan were cross-linked with ethylene glycol diglycidyl ether (EGDE). Deprotection of amino groups was carried out with hydrochloric acid.…”
Section: Synthesis Of Cross-linked Chitosanmentioning
confidence: 99%