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¸½¼þÎÒÎÄÕµÄ˵Ã÷£ºThe chemical structure of pyrolytic cellulose and cellulose was analyzed using FTIR. The infrared spectra are presented in Fig. 4. They were both characterized with dominant O-H stretching (3200-3500 cm-1) and C-H stretching (2850-3000 cm-1) corresponding to the aliphatic moieties. For cellulose, the O-H bending vibration frequencies at 1640 cm-1 demonstrated that the sample combined micro amount of water. The strong absorption peak at 1059 cm-1 should be the stretching vibration of C-O bond in cellulose, as well as the C-O bond in hemiacetal of pyranose [16, 17]. Compared with cellulose, the peaks at 2921 cm-1 and 2852 cm-1 indicated that there were paraffin waxes or its derivatives in the pyrolytic celluclose. The peaks at 1704 and 1621 cm-1 were C=O and C=C stretching, respectively, which resulted from the removal of water from cellulose by pyrolysis. It agreed well with the Py-GC/MS results which contained a large amount of paraffin waxes, ketones, carboxylic acids, and alkenes. C=C-H bending vibration in plane was at 800 cm-1. The stretching vibrations of C-O bond (1059 cm-1) and the typical values of ¦Â-D-glucoside (897 cm-1) were weaken.

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