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  • Electronic Resource  (4)
  • microstructure  (2)
  • poly(maleic anhydride)  (2)
  • 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
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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. 1313-1327 
    ISSN: 0887-624X
    Keywords: microstructure ; PP-g-MA ; PAmXD,6 ; blends ; melt viscosity ; specific interfacial area ; interfacial copolymer concentration ; Brabender torque ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work deals with the relationship between microstructure, melt viscosity, and copolymer concentration of PAmXD,6/PP-g-MA blends [poly(m-xylylene adipamide)/maleic anhydride functionalized polypropylene]. The blends were processed in a Brabender plastograph at a temperature of 265 ± 5°C and at 45 rpm. The characterization of the microstructure was carried out through SEM analysis after microtome leveling and chemical etching. The melt viscosity of the components and of the blends was measured by the Brabender torque. It was found that the copolymers concentration controls the dimension of the dispersed phase. The composition of the blend (dispersed phase weight percent) has a more limited influence. Variations of the components viscosity ratio during the mixing time have little, if any influence on the dimension of the dispersed phase. A linear relation between the Brabender torque and the specific interfacial area was found. The determination of the copolymer weight fraction leads to the establishment of a close relation between the copolymer concentration and the specific interfacial area. For blends containing from 0 to 7.5 wt % of copolymer, this relation is linear and consequently the concentration of copolymer at the interface is constant at about one copolymer macromolecule per 16 nm2. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1313-1327, 1997
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    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
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1727-1736 
    ISSN: 0887-6266
    Keywords: polysilane ; microstructure ; mesophase ; liquid crystal ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The physical structure of poly(methylphenyl) silane (PMPS) has been investigated using wide-angle x-ray scattering at various temperatures and optical polarizing microscopy. The results obtained by these techniques clearly show the existence of an ordered phase in PMPS. The crystallinity of our sample was estimated to be about 10% at room temperature. Below 190°C, the atactic chains pack into a monoclinic crystalline lattice of near hexagonal symmetry, with two types of disorder existing in the packing. At about 190°C, a phase transition to a liquid crystalline columnar hexagonal packing (Dho) occurs. Finally, the sample melts into an isotropic amorphous phase. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1727-1736, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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