2007
DOI: 10.1016/j.carbpol.2006.05.023
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Radiation-induced degradation of carboxymethylated chitosan in aqueous solution

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Cited by 52 publications
(21 citation statements)
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“…There are many reports of the radical-scavenging properties of chitosan and its derivatives [13], but there is some disagreement between the results of different studies. Scavenging of HO • by chitosans of various molecular weights was consistently reported [14,38,39] and is supported by results demonstrating depolymerisation of the polysaccharide chain by HO • [40][41][42][43], although one study led to the unlikely conclusion that sulfated chitosan did not react with this radical [44]. Kinetic measurements have confirmed that the reaction of HO • with carbohydrates is close to diffusion control, with reported rate constants between 1.64 × 10 9 M −1 s −1 for monosaccharides and 1.8 × 10 8 M −1 s −1 for glycogen with 3000 glucose subunits [45][46][47].…”
Section: Discussionsupporting
confidence: 52%
“…There are many reports of the radical-scavenging properties of chitosan and its derivatives [13], but there is some disagreement between the results of different studies. Scavenging of HO • by chitosans of various molecular weights was consistently reported [14,38,39] and is supported by results demonstrating depolymerisation of the polysaccharide chain by HO • [40][41][42][43], although one study led to the unlikely conclusion that sulfated chitosan did not react with this radical [44]. Kinetic measurements have confirmed that the reaction of HO • with carbohydrates is close to diffusion control, with reported rate constants between 1.64 × 10 9 M −1 s −1 for monosaccharides and 1.8 × 10 8 M −1 s −1 for glycogen with 3000 glucose subunits [45][46][47].…”
Section: Discussionsupporting
confidence: 52%
“…2. The increase in the height of the peak at 290 nm could be due to the formation of a carbonyl group in laminarin (Huang, Zhai, Peng, Li, & Wei, 2007;Yoksan, Akashi, Miyata, & Chirachanchai, 2004). The glycosidic bond in laminarin was broken down to carbonyl groups by the hydroxyl radicals generated by gamma irradiation.…”
Section: Uv-vis Absorptionmentioning
confidence: 95%
“…To confirm the carbonyl group formation, Infrared spectra were obtained. The absorption peak at 1630 cm À1 appeared in Fourier transform infrared (FT-IR) spectra of the gamma irradiated laminarin, which was attributed to the absorbance of carbonyl groups (Huang et al, 2007;Tian, Liu, Hu, & Zhao, 2004). The height of this peak was increased at higher dose.…”
Section: Uv-vis Absorptionmentioning
confidence: 98%
“…The broad band between 3420 and 3100 cm -1 due to the -OH stretching vibration is observed. This peak is referred to asymmetry stretching of alcoholic hydroxyl group bonded with water molecule in the hydrogel (32) . On the other hand, curve c shows a band at high wave number appeared at 1638 cm -1 .…”
Section: Timementioning
confidence: 99%
“…Peaks at 1412 cm -1 were assigned to C-O stretch vibration of -COOH. These changes in spectra revealed that although CMCt were cross-linked after irradiation, radiation degradation lead to formation of new carbonyl groups formed and some -NH 2 were scissored out (32) .…”
Section: Timementioning
confidence: 99%