2006
DOI: 10.1016/j.carbon.2005.12.002
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Physical and chemical properties of carbons synthesized from xylan, cellulose, and Kraft lignin by H3PO4 activation

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Cited by 213 publications
(124 citation statements)
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“…Stretching vibration at 1,400-1,600 cm -1 corresponds to the aromatic ring or C=C bonding. Presence of this functional group indicates the formation of carbonylcontaining group and aromatization of the precursor [22]. While the band around 1,200 cm -1 is typically represented by the C-O group.…”
Section: Moisture Contentmentioning
confidence: 99%
“…Stretching vibration at 1,400-1,600 cm -1 corresponds to the aromatic ring or C=C bonding. Presence of this functional group indicates the formation of carbonylcontaining group and aromatization of the precursor [22]. While the band around 1,200 cm -1 is typically represented by the C-O group.…”
Section: Moisture Contentmentioning
confidence: 99%
“…The band at ~2900 cm -1 is ascribed to C-H axial deformation [18] and the band with its maximum located at 1770 cm -1 is attributed to lactones. The band near 1600 cm -1 is due to C=C stretching vibration in the aromatic ring and is observed for all samples with a very small shift; bands in the region 1000-1300 cm -1 can be attributed to various C-O bands such as those in ethers, phenols, and esters [19]. The bands in the region 850-440 cm -1 are ascribed to alkene vibrations.…”
Section: Ash Content Ph Of Supernatant Ph Pzc and Base Neutralizamentioning
confidence: 93%
“…In CSAC, the wide band in the range of 3804-3200 cm -1 corresponds to the presence of O-H stretching vibration in hydroxyl groups [20]. The band at 1705 cm -1 is attributed to the stretching vibration of C=O in ketones, aldehydes, lactones, and carboxyl groups [21] and the band at about 1570 cm -1 is assigned to C=C vibration in aromatic rings [22]. These bands reflect the biological origin of the precursor.…”
Section: A Xrd Analysismentioning
confidence: 99%