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446                Polymer-based Nanocomposites for Energy and Environmental Applications

         extracted from the bioethanol plant was purified by soxhlet extraction for 6 h at 150°C
         using a toluene/acetone mixture (2:1 ratio) by eliminating extracts. This material was
         then washed with the help of mixture having 700 mL deionized water, 6.7 g sodium
         chloride, and 1.5 mL acetic acid, at 70°C for 12 h. Acetic acid and sodium chloride
         were consecutively added after every 2 h and stand out for another 12 h, and a pure
         white material was developed. After 24 h, the matter was washed with deionized water
         and reduced to 17 wt% solid amount by centrifugation. The purified cellulose was
         concentrated to 2 wt% suspensions; after mixing with shear mixture, it delivered
         by the APV 2000 high-pressure homogenizer (Denmark) at a pressure of 500 bar. This
         suspension was homogenized 10 times to get a thick gel of nanocrystalline
         cellulose (NCC).




         16.2.4 Chitin nanocrystals from carb shell residue

         Gopalan Nair and Dufresne [35] were reported the development of chitin nanocrystals
         (ChNC). Crab shell residue was subjected to alkali action, acid hydrolysis, and
         bleaching. Chitin flakes were boiled, in order to remove proteins, in a 5% KOH solu-
         tion for 6 h. After that, hydrolysis of hydrochloric acid (HCl) for 90 min at boiling
         temperatures was performed following the bleaching with chlorite for 6 h at 80°C.
         Finally, chitin nanocrystal suspensions were developed subsequently after hydrolysis
         of acid (3 N HCl) and sonified before applying.




         16.3    Preparations of surface modified
                 bionanocomposites


         16.3.1 TEMPO (2,2,6,6, tetramethyl-1-piperidinyloxy)-mediated
                  oxidation

         This TEMPO-mediated oxidation technique was performed like the method
         accounted by Saito et al. [36]. In TEMPO-mediated oxidation technique, the cellulose
         sludge, slurry was mechanically compressed; latter on it was dispersed in a solution of
         NaBr and TEMPO (1 and 0.1 mmol/g of pulp residue, respectively). The concentra-
         tion of the pulp residue was adjusted 2 wt% in water. The reaction was carried out by
         the addition of NaClO slowly into the suspension following the pH around 10 by
         NaOH addition. Thereafter, different oxidation degrees were reached by selecting dif-
         ferent quantities of NaClO (1, 3, 6, and 10 mmol/g of pulp residue). Finally, NaClO
         was consumed; then, the filtered and rinsed cellulose fibers were mixed in water and
         disintegrated in a microfluidizer M-110Y (Microfluidics Ind., the United States) to
         develop TOCNF suspension. Likewise, TEMPO-oxidized chitin nanofibers from chi-
         tin powder were developed according to the same technique by using 10 mmol/g of
         NaClO [37].
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