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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1713-1721 
    ISSN: 0887-624X
    Keywords: polyurethane anionomers ; ionic diols ; methylene spacers ; TGA ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionic diols with varying methylene spacers were prepared from maleic anhydride and linear diols. Reaction across the unsaturated site by aqueous sodium bisulphite was used to prepare the ionic diols. Chain extended polyurethane ionomers were prepared by the reaction of prepolymer based on different polyols and diisocyanates with the ionic diols. The polyurethane anionomers were characterized by FT-IR and FT-NMR spectroscopy. The differential scanning calorimetric results show that Tg of the anionomers shifted towards low values as the ionic content in the polyurethane increases and as the length of the ionic diol increases. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 1237-1244 
    ISSN: 0887-624X
    Keywords: polyurethane ionomers ; iniferters ; “living” radical polymerization ; tetraphenylethane derivatives ; vinylbenzyl chloride ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyurethane iniferter prepared from isocyanate end capped prepolymer and 1,1,2,2-tetraphenyl-1,2-ethanediol, has been used to polymerize vinylbenzyl chloride to obtain polyurethane-polyvinylbenzyl chloride multiblock copolymers. Formation of the block copolymers proceeds with increase in both molecular weight and conversion with increasing polymerization time showing that the polymerization proceeds via a “living” radical mechanism. The block copolymers so obtained were converted into their cationomers by the treatment of triethylamine. The block copolymers and their cationomers have been characterized by FTIR, FTNMR, TGA, and DSC studies. The effect of thermal energy on the molecular weight of the macroiniferter in the absence of monomer has been studied in order to understand the mechanism of formation of the block copolymers. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1237-1244, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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