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2000
DOI: 10.1023/a:1002880411320
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Cited by 30 publications
(12 citation statements)
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“…The changes that occurred on the internal structure of the prepared hydrogel could be investigated using X-ray diffraction techniques. The X-ray diffraction pattern of chitosan (Figure 4) demonstrated two peaks, assigned to its amorphous and crystalline sections at the diffraction angles (2θ) 10° and 20°, respectively [32]. This can be ascribed to the existence of numerous OH and NH2 functional groups with high polarity, which allow for the formation of potent intra-and intermolecular hydrogen bonds.…”
Section: X-ray Diffraction Of the O-cm-chitosan Hydrogelmentioning
confidence: 99%
“…The changes that occurred on the internal structure of the prepared hydrogel could be investigated using X-ray diffraction techniques. The X-ray diffraction pattern of chitosan (Figure 4) demonstrated two peaks, assigned to its amorphous and crystalline sections at the diffraction angles (2θ) 10° and 20°, respectively [32]. This can be ascribed to the existence of numerous OH and NH2 functional groups with high polarity, which allow for the formation of potent intra-and intermolecular hydrogen bonds.…”
Section: X-ray Diffraction Of the O-cm-chitosan Hydrogelmentioning
confidence: 99%
“…This observation was in accordance with many previous studies. A peak at a 2θ of approximately 10.2° corresponded to hydrated crystals, and the one around a 2θ of 19.8° belonged to anhydrous crystals because of the intermolecular and intramolecular hydrogen bonding of CS . After radiation‐induced grafting [Figure (B‐b–d)], the basic diffraction peaks were maintained, but some peak intensities changed considerably, and a new peak evidently appeared.…”
Section: Resultsmentioning
confidence: 99%
“…X-ray diffractometry was used to explore the inner structures of the modified chitosan derivatives and their X-ray diffraction patterns were shown in Figure 3. There were two broad peaks in chitosan appeared near to 2θ = 10 • and 20 • which were attributable to its amorphous and crystalline regions, respectively [29]. This can be ascribed to the formation of the hydrogen bonds along its chains due to its possession of a great number of hydroxyl and amino groups.…”
Section: Powder X-ray Diffraction Of Ccs Adsorbentmentioning
confidence: 97%