2011
DOI: 10.1016/j.carbpol.2010.11.013
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Synthesize and properties of photosensitive organic solvent soluble acylated chitosan derivatives (2)

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Cited by 19 publications
(5 citation statements)
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“…Figure d displays the XRD diffractograms of the hydrogels before and after cross-linking. The strongest reflection appeared at 2θ ∼ 11.0 and 20.4° of CS are assigned to crystal forms I and crystal forms II, respectively. After covalent cross-linking, the peaks of CS–ECH at 2θ ∼ 11.4° and 2θ ∼ 20.8° become wider and weaker, which is due to the destruction of hydrogen bonding of CS during the cross-linking reaction .…”
Section: Resultsmentioning
confidence: 98%
“…Figure d displays the XRD diffractograms of the hydrogels before and after cross-linking. The strongest reflection appeared at 2θ ∼ 11.0 and 20.4° of CS are assigned to crystal forms I and crystal forms II, respectively. After covalent cross-linking, the peaks of CS–ECH at 2θ ∼ 11.4° and 2θ ∼ 20.8° become wider and weaker, which is due to the destruction of hydrogen bonding of CS during the cross-linking reaction .…”
Section: Resultsmentioning
confidence: 98%
“…In the spectrum of the cellulose hydrogel, the bands at 1732, 1572, and 1406 cm −1 which were assigned to the CO stretching vibration of the ester group, asymmetric CO stretching vibration of the carboxylate in BTCA, and symmetric CO stretching vibration of the carboxylate in BTCA, respectively 20. In the case of the chitin hydrogel, the characteristic amide I band at 1660 cm −1 and the amide II band at 1550 cm −1 were observed 28. In the spectrum of the cellulose/chitin hybrid hydrogel prepared at the BTCA feed ratio of 1, the bands at 1732, 1660, 1572, 1550, and 1406 cm −1 were observed, indicating that the cellulose and chitin were crosslinked by esterification with BTCA.…”
Section: Resultsmentioning
confidence: 99%
“…Figure d displayed the XRD diffractogrames of CS and CS-ECH. The strongest reflection appeared at 2θ = 20.0° and 10.0° were assigned to crystal forms II and crystal forms I, respectively. After cross-linking, the peak at 2θ = 20.0° was weaker and became broader, and the peaks at 2θ = 10.0° disappeared which was due to the destruction of hydrogen bonding between amino groups and hydroxyl groups of chitosan during the cross-linking reaction …”
Section: Resultsmentioning
confidence: 99%