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  • 1
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Homogeneous graft copolymerization of styrene onto cellulose was carried out using a SO2-DEA-DMSO cellulose solvent reaction medium and γ-ray mutual irradiation. The yield of grafted side chain polymer and the homopolymer in this reaction system proved to be polysulfone, a styrene-sulfur dioxide copolymer in which the number of sulfur atoms per polymer chain is 3-3.5. Several characterizations of the graft product were attempted. The graft products were extracted with boiling benzene for 24 hr to remove homopolymer, and then the cellulose backbones were hydrolyzed. After hydrolysis, the polysulfone residues were separated by thin-layer chromatography (TLC) into two components, i.e., attendant homopolysulfone and the true side chain polysulfone having some sugar residues at one of the polymer chain ends. The weight fraction of these components for each graft product was determined by a TLC scanner. The molecular weight of the side chain polysulfone remained constant and significantly lower than that of the homopolysulfone throughout the reaction period. By assuming that no scission of cellulose chains occurred throughout the graft reaction, the number of branches per starting cellulose molecule was assessed to be surprisingly large, ranging from 2.4 to 10.6 at a total dose of 1-8 mR of irradiation. It was also found that percent grafting increased with irradiation time because of an increase in the number of branches per cellulose chain. Furthermore, we succeeded in separating the graft product into ungrafted cellulose and the true graft copolymer containing a small amount of attendant hompolysulfone.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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