2015
DOI: 10.1016/j.carbpol.2015.05.077
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NaOH treatment of chitosan films: Impact on macromolecular structure and film properties

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Cited by 86 publications
(62 citation statements)
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“…Chitosan powder exhibited 2 well‐defined peaks centered at 10.6°and 20.2°. This agrees with previous findings of Xu et al and Takara et al After making the film, the peak at 10.6° was no longer observed; instead, a new peak appeared at 8.1°. The peak at 20.2° broadened markedly, and the broadening indicates that the chitosan transitions to a highly amorphous state during the film preparation.…”
Section: Resultssupporting
confidence: 93%
See 1 more Smart Citation
“…Chitosan powder exhibited 2 well‐defined peaks centered at 10.6°and 20.2°. This agrees with previous findings of Xu et al and Takara et al After making the film, the peak at 10.6° was no longer observed; instead, a new peak appeared at 8.1°. The peak at 20.2° broadened markedly, and the broadening indicates that the chitosan transitions to a highly amorphous state during the film preparation.…”
Section: Resultssupporting
confidence: 93%
“…Cellulose nanocrystal exhibited 3 characteristic peaks at 2θ=17°(plane 110), 21°(plane 102), 22.5°(plane 200), and 34°(plane 004), which corresponded to typical crystalline cellulose I structure. 43 Chitosan powder exhibited 2 well-defined peaks centered at 10.6°and 20.2°.This agrees with previous findings of Xu et al39 and Takara et al44…”
supporting
confidence: 87%
“…The effect of C NaOH is negligible, at least when hydrogels from CS solutions at C CS > C* are considered. Such a finding is in line with recent results by Takara et al on the Young's modulus of CS films . It can be argued that the network structure above the overlap concentration is stable enough not to be appreciably altered by the rate of pH‐induced gelation.…”
Section: Resultssupporting
confidence: 91%
“…The FTIR spectra of chitosan and chitosan/iron nanocomposites are shown in Figure 8. The dominant bands appearing in the neat chitosan are due to the vibrations of functional groups such as symmetrical stretching vibrations of N-H at 3356 cm -1 , stretching of Journal of Nanomaterials -OH bonds corresponding to the strong and broadband centered at 3288 cm -1 [5], asymmetric stretching vibrations of C-H bonds at 2920 cm -1 , and stretching of C-H at 2874 cm -1 . Furthermore, vibrations of carbonyl bonds of the secondary amide group at 1647 cm -1 , C=O vibrations in the protonated amine group at 1566 cm -1 , CH bending of methylene at 1420 cm -1 , and a methyl group at 1377 cm -1 also indicate the characteristic peaks of chitosan.…”
Section: Chemicalmentioning
confidence: 99%
“…It is the linear polymer of β-(1-4)-2-acetamido-2-deoxy-D-glucopyranose synthesized by deacetylation of chitin, the second most abundant polysaccharide in nature. Chitin is extracted by the exoskeleton of crustaceans such as shrimps and crab shells [5][6][7]. Chitosan exhibits superior properties such as nontoxicity, biodegradability, biocompatibility, antiviral, and antimicrobial properties [8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%