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Scheme showing hydrogen bonding (-) and carboxymethylation of cellulose. 

Scheme showing hydrogen bonding (-) and carboxymethylation of cellulose. 

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In this work, CMC was synthesized from cellulose obtained from coir fibres. The obtained CMC yield was about 64.0%. The Degree of Substitution value obtained was 0.44. The spectral pattern and thermogravimetric analysis of the synthesized CMC and cellulose were evaluated using FT-IR, XRD, and TGA/DTG. Characterization of the cellulose and CMC revea...

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... in this study a comparative spectral analysis of the synthesized CMC and cellulose obtained from coir fibre via a green synthetic method (hydrogen peroxide liquid phase oxidation of cellulose) was carried out and studied using FT-IR, XRD and TGA/DTG. Figure 1 shows a schematic representation of carboxymethylation process which proceeds via SN2 mechanism. The amount of hydrogen bonding obtained in CMC as compared to ordinary native cellulose reduces due to the etherification of OH group in native cellulose [2,32]. ...

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... The peak at 2895 cm −1 in untreated sugarcane bagasse is attributed to C H stretching in methyl and methylene groups. 31 The absorption band (2885 cm −1 ) found by other researchers was intangible compared to the results of this study. 16 The bands at 1604 cm −1 , 1319 cm −1 , 1242 cm −1 , and 1158 cm −1 in untreated sugarcane bagasse are attributed, respectively, to the stretching vibrations of N H bending (amine), O H bending, C O stretching (acetyl), and N H stretching (organic sulfate). ...
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... The absorption bands at 2908.65 and 2910.58 cm -1 for the NaOH treated coir fibres and untreated coir fibre, respectively, may be attributed to C-H stretching in methyl and methlyene groups (Ikhuoria et al. 2017). The absorption band at 1724.36 cm -1 in untreated coir fibre corresponds to the carbonyl (C=O) stretching vibrations of carboxyl and acetyl groups in hemicelluloses. ...
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