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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. 1195-1202 
    ISSN: 0887-624X
    Keywords: poly(maleic anhydride) ; polypropylene ; PP-g-MA ; size exclusion chromatography ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The homopolymerization of maleic anhydride was attempted at 190°C, during the melt-functionalization of polypropylene, either with or without organic peroxide using a Brabender plastograph. The free radical homopolymerization of pure maleic anhydride was also attempted either with or without organic peroxide, at 190°C, in vacuum-sealed glass vials. In all cases, free low molecular weight maleic anhydride oligomers were observed by low molecular weight size exclusion chromatography (SEC). This maleic anhydride homopolymerization tends to prove that the ceiling temperature of poly(maleic anhydride) probably lies above the previously published value of 160°C for these specific experimental conditions. © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 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. 901-915 
    ISSN: 0887-624X
    Keywords: blend ; PP-g-MA ; PAmXD,6 ; maleic anhydride ; poly(maleic anhydride) ; imidization ; amine-anhydride reaction ; compatibilization ; molecular weight segregation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work deals with the study of PAmXD,6/PP-g-MA blends [poly(meta-xylylene adipamide)] and (maleic-anhydride-functionalized-polypropylene) blends. Compatibilization occurs during the blending of the components in a Brabender plastograph at 265 ± 5°C and at a mixing rate of 45 rpm. Kinetic data from the literature indicate that the rate of amine/anhydride reaction is much faster than the rate of amide/anhydride reaction. This interpretation is confirmed by the use of model systems constituted of PAmXD,6 and pyromellitic dianhydride or of PP-g-MA and meta-xylylene diamine. Infrared analyzes of extracted nodules of PAmXD,6/PP-g-MA blends also confirm the extent of the imidization and show that the length of the PAmXD,6 blocks is lower than the free PAmXD,6 one. Segregation mechanisms during the compatibilization are discussed to explain this observation. The structure of the copolymers was deduced from those results and from the previous characterizations of PP-g-MA and PAmXD,6. It consists in a block of PP linked with some blocks of PAmXD,6. The average number of PAmXD,6 blocks depends on the average length of the poly(maleic anhydride) functionality carried on by PP-g-MA. © l997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 901-915, 1997
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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