## Abstract A mechanism for ozone–olefin reactions is developed that is consistent with the recent findings of several investigations. These findings suggest a reaction sequence leading to the production of fewer free radical species than has been assumed in the past. Computer simulations using the
Crosslinking of chitosan fibers with dialdehydes: Proposal of a new reaction mechanism
✍ Scribed by Jonathan Z. Knaul; Samuel M. Hudson; Katherine A. M. Creber
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 281 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-6266
No coin nor oath required. For personal study only.
✦ Synopsis
A highly deacetylated chitosan from shrimp with a degree of deacetylation of 95.28 Ϯ 3.03% was prepared and spun into a monofilament fiber using a solution of 4% (w/v) chitosan in 4% (v/v) aqueous acetic acid. Samples of the spun fibers were immersed in aqueous solutions containing glutaraldehyde and glyoxal, and subsequently washed and dried. When the concentration of crosslinking agent was varied at room temperature over a constant time of 1 h, dry mechanical properties improved up to a point after which increasing concentrations resulted in degradation. Immersion time was also varied between 1 and 60 min at 25.8°C, and temperature was varied between 25.8 and 70.0°C, at fixed concentrations of both glyoxal and glutaraldehyde. It was demonstrated that mechanical improvements might be rendered at higher temperatures over lesser times. However, it was also shown that at higher temperatures, fiber mechanical properties would begin to diminish. Chitosan films were subjected to similar treatments in aqueous crosslinking solutions. Fourier transform infrared data (FTIR) on the films suggest that some interaction is occurring between the glutaraldehyde or glyoxal and the amine group on the chitosan backbone.
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