2006
DOI: 10.1016/j.molstruc.2006.03.018
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Drying process of microcrystalline cellulose studied by attenuated total reflection IR spectroscopy with two-dimensional correlation spectroscopy and principal component analysis

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Cited by 81 publications
(79 citation statements)
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“…From vibrational spectroscopic studies, it can be seen that wood-water interactions are dominated by interactions with O-H groups (hydroxyls), since deuteration only affects O-H vibrations, while C-H stretching vibrations remain unchanged and no C-D stretching vibrations are observed (Hofstetter et al 2006;Mann and Marrinan 1956a;Schmidt et al 2006;Taniguchi et al 1966;Watanabe et al 2006). After deuteration and drying, the relative accessibility of hydroxyls to water can be determined as the ratio of integrated areas of O-D to the sum of O-H and O-D vibrations (Suchy et al 2010b;Taniguchi et al 1966) or alternatively as the ratio of weighted intensities of O-D to the sum of O-H and O-D vibrations (Mann and Marrinan 1956b;Sepall and Mason 1961).…”
Section: Vibrational Spectroscopymentioning
confidence: 99%
“…From vibrational spectroscopic studies, it can be seen that wood-water interactions are dominated by interactions with O-H groups (hydroxyls), since deuteration only affects O-H vibrations, while C-H stretching vibrations remain unchanged and no C-D stretching vibrations are observed (Hofstetter et al 2006;Mann and Marrinan 1956a;Schmidt et al 2006;Taniguchi et al 1966;Watanabe et al 2006). After deuteration and drying, the relative accessibility of hydroxyls to water can be determined as the ratio of integrated areas of O-D to the sum of O-H and O-D vibrations (Suchy et al 2010b;Taniguchi et al 1966) or alternatively as the ratio of weighted intensities of O-D to the sum of O-H and O-D vibrations (Mann and Marrinan 1956b;Sepall and Mason 1961).…”
Section: Vibrational Spectroscopymentioning
confidence: 99%
“…Marked changes in the bands at 3386,2963,2935,2874,1732,1457, and 1134 cm -1 were observed. The broad peak centered at 3386 cm -1 representing O-H stretching vibration, and the intensity of this band decreased in spectrum 2c; in addition, the peak position showed a blue shift, which is likely because the hydrogen bonds between the hydroxyl groups of the LS molecule were destroyed when O-H groups were substituted to form butyryl groups (Watanabe et al 2006). The increased intensity of C-H stretching peaks at 2963, 2935, 2874, and 1457 cm -1 indicate that new C-H bonds were introduced into the LS.…”
Section: Analysesmentioning
confidence: 99%
“…In particular, absorbance due to C-O stretching, C-O-C asymmetric stretching, COH and CCH deformation vibrations, and CH 2 wagging are observed at 1,000-1,300 cm -1 as well as O-H stretching at 2,600-3,500 cm -1 (Proniewicz et al 2001;Watanabe et al 2006;Zhang et al 2009). Similar to previous studies, curve e shows that characteristic cellulose I peaks at these regions lose definition and broaden as crystallinity is lost when cellulose I is converted to cellulose II (Proniewicz et al 2001;Watanabe et al 2006;Zhang et al 2009). Fiber welded samples (curves b, c, d) show a progression of increased cellulose II character with additional treatment time.…”
Section: Chemical Propertiesmentioning
confidence: 99%