2013
DOI: 10.1016/j.carbpol.2013.02.012
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Polymorphic transformation of cellulose I to cellulose II by alkali pretreatment and urea as an additive

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Cited by 107 publications
(55 citation statements)
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“…The second hatched area contains the out-of-plane stretching vibrations of CH bonds in the aromatic rings of crystalline cellulose, as well as the stretching vibrations of CH and COC bonds in the β-(1,4)-glycosidic linkages between the anhydroglucose units. Polymorphism has already been documented for NaOH-treated cellulose [50]. The absorption band at 1160 cm −1 is due to crystalline cellulose (COC asymmetrical stretching).…”
Section: Resultsmentioning
confidence: 94%
“…The second hatched area contains the out-of-plane stretching vibrations of CH bonds in the aromatic rings of crystalline cellulose, as well as the stretching vibrations of CH and COC bonds in the β-(1,4)-glycosidic linkages between the anhydroglucose units. Polymorphism has already been documented for NaOH-treated cellulose [50]. The absorption band at 1160 cm −1 is due to crystalline cellulose (COC asymmetrical stretching).…”
Section: Resultsmentioning
confidence: 94%
“…Thus, the high sensitivity of the activation energy of 240 dissolution value on DP indicates that the cellulose dissolution has been critically controlled by 241 DP value (Qi, Chang & Zhang, 2008). However, the solubility of cellulose samples was not 242 significantly increased with the decreased DP values (Table 1) inter-chain but also inter-plane hydrogen bonds (Gupta, Uniyal & Naithani, 2013). Moreover, 250 upon evaporation of the ammonia, the cellulose I structure reforms its intrasheet hydrogen bonds 251 but settles into the nearest energy minimum forming cellulose III (Sarko, Southwick & Hayashi, 252 1976).…”
Section: Influence Of Crystal Type On Dissolution 236mentioning
confidence: 85%
“…Diffractograms displayed three main characteristic peaks assigned to cellulose I in X-ray diffractions, and these are located at approximately 2h = 14°, 16°and 22°Corresponding to 1 1 0 (d 1 spacing), 1 1 0 (d 2 spacing) and 2 0 0 (d 3 spacing) crystallographic planes respectively. The diffractogram peak located at around 2h = 35°, corresponds to 0 4 0 crystallographic plane [37,38]. The X-ray diffractograms, showed no change in peak intensities located at the crystallographic plane reflections, indicating no transformation of cellulose I into cellulose II allomorph due to ultrasonication.…”
Section: X-ray Diffraction Analysis (Xrd)mentioning
confidence: 92%