An effective condition of graft polymerization of acrylonitrile onto cellulose fiber in large volume of KMnO 4 /citric acid aqueous solution was examined and the produced grafted copolymers were characterized by using SEM, NMR, FTIR, XRD, TGA, and DSC in comparison with component homopolymers. Graft yield, GY, obtained by simple weighting method was close to the value obtained by NMR analysis. Significant change of chemical structure in cellulose fiber, other than graft reaction, was not detected by NMR and FTIR measurements, whereas a decrease in the degree of crystallinity by the reaction was detected by XRD measurement. It was pointed out that thermograms for grafted samples resembles with that of cellulose at T < 370 C and become similar with that for polyacrylonitrile at T > 370 C and the mass of residue at 550 C is proportional to the content of polyacrylonitrile (GY) only. It is concluded that thermal decomposition of both polymers occurs almost independently in grafted polymers and thermal stability of cellulose fiber is not improved.

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Derivatives of formyl pyrazole were synthesized by the reaction of acetophenone, 4-methyl acetophenone, 3-acetyl furan, 3-acetyl thiophen and phenyl hydrazine derivatives. The product was treated with Vilsmeier reagent producing different formyl pyrazole derivatives which were characterized by FT-IR, 1HNMR, Elemental analysis and Mass spectroscopy. The formyl pyrazole derivatives were reacted with chitosan to produce chitosan/ pyrazole Schiff base. These Schiff bases were characterized by FT-IR and TGA.The antimicrobial activity of chitosan/ pyrazol Schiff base (CSB) was evaluated against Gram-positive bacteria (Staphylococcus aureus and Bacillus cereus), gram negative bacterium (Escherichia coli) and fungus (Aspergillus niger). Results indicated agood inhibitory activity for CSB-14 when tested against B.cereus that gave inhibition zone of 7.5 ± 0.6 (mm), however CSB-18 gave a pronounced inhibitory activity against S. aureus and recorded 25 ± 2.0 (mm). All synthesized derivatives have no inhibitory activity against Gram negative E. coli. CSB-14, and CSB-15 exhibited inhibitory activity against tested A. niger that was used as a fungal model which gave 19 ± 0.9 and 18 ± 1.0 inhibition zone (mm) respectively. Thus, these results showed that, functionalization of chitosan with the hetero-cyclic compounds created biological activities of the synthesized derivatives; hence the synthesized pyrazole derivatives have not recorded any inhibitory activity before its immobilization onto chitosan.

Cellulose-graft-polyacrylonitriles were prepared by using KMnO 4 /different acids redox system and the obtained samples were characterized by POM, SEM, 13 C-NMR, XRD, TGA and their mechanical properties were investigated as a function of crystallinity degree (Cr %). In all cases, Cr decreased with increase of graft yield irrespective of acids species. Stress at break, strain at break and Young's modulus decreased with decreasing Cr %, which can be attributed to the increase of the amorphous region and the main chain rapture of cellulose. The mechanical properties of the samples prepared by strong acids became more poor than those for samples prepared by weak acids, indicating that more chain rupture occurred when strong acids are used.

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