2009
DOI: 10.1016/j.jnoncrysol.2009.09.016
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Preparation, vibrational structure and dielectric properties studies of cotton linter and its derivatives

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Cited by 9 publications
(7 citation statements)
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“…The LOI compares the peak intensity at ∼1429 cm −1 attributed to δ OH of C6–O6H in crystalline regions to the peak intensity at ∼896 cm −1 associated with amorphous cellulose. 55 The TCI compares the peak intensity at 1372 cm −1 associated with δ OH with that of the 2860 cm −1 peak due to ν CH, 56 and the hydrogen bonding index (HBI) compares the ratio of intensities of the peaks at 3345 cm −1 ν OH due to intra and intermolecular hydrogen bonding 57 and 1337 cm −1 due to δ OH of O2H and O3H. 58 We assessed LOI, TCI and HBI during the first ∼5 hours of the reaction where peaks in the hydride-OH region were clearly distinguishable (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…The LOI compares the peak intensity at ∼1429 cm −1 attributed to δ OH of C6–O6H in crystalline regions to the peak intensity at ∼896 cm −1 associated with amorphous cellulose. 55 The TCI compares the peak intensity at 1372 cm −1 associated with δ OH with that of the 2860 cm −1 peak due to ν CH, 56 and the hydrogen bonding index (HBI) compares the ratio of intensities of the peaks at 3345 cm −1 ν OH due to intra and intermolecular hydrogen bonding 57 and 1337 cm −1 due to δ OH of O2H and O3H. 58 We assessed LOI, TCI and HBI during the first ∼5 hours of the reaction where peaks in the hydride-OH region were clearly distinguishable (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the occurrence of intense bands such as 1520.8, 1442.70 and 1381.90, and 535.90cm -1 which falls within 1600 -1300 and 800 -600cm -1 respectively are in support of the fact that the broad band is due to hydrogen-bonded OH adsorption of a hydroxyl (alcohol) functional group. The band around 2925.30cm -1 is due to the methylene carbon-hydrogen bond (C-H) stretching vibration [11][12][13]. The major band in the region of 1630.90 cm -1 is usually indicative of the presence of a carbonyl compound.…”
Section: Resultsmentioning
confidence: 99%
“…There is a relaxation at frequency 10 5 to 10 6 Hz, which should be the rotation process of the end nitro-groups responding to the alternating eld even at high frequencies. 34 The relaxation at 10 3 Hz is considered to be the reorientation of the side-group nitrophenyl moieties, which is caused by the polarization of the molecular permanent dipole moments. 35,36 The strong inherent moment of nitrophenyl moieties enables them to reorient in response to external electric elds.…”
Section: Resultsmentioning
confidence: 99%