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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. 1039-1047 
    ISSN: 0887-624X
    Keywords: PAmXD,6 ; Brabender plastograph ; hydrolysis ; condensation ; equilibrium constant ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: PAmXD,6 [poly(m-xylylene adipamide)] was processed using a Brabender plastograph at 30 rpm and at 265 ± 5°C. The evolution of the Mn versus mixing time determined from solution viscosity and chain end concentrations measurements shows that PAmXD,6 undergoes hydrolysis or condensation reactions depending on its initial molecular mass. Lower masses undergo condensation while higher masses undergo hydrolysis. The determination of water concentration in the melt during mixing time confirmed that this behavior is related to an equilibrium constant which was estimated at 500 ± 100. For a mixing period shorter than 20 min, a good correspondence was observed between Mn values determined either by chain end concentrations or by solution viscosity. However, for a mixing period longer than 20 min, discrepancy between Mn values using both methods witnesses the probable appearance of oxidative degradation of PAmXD,6. Mechanisms adapted from the established oxidation reactions of PA6 and PA6,6 are proposed to justify the PAmXD,6 behavior. Those reactions could explain the slight yellowing of PAmXD,6 during its processing. It was also shown that the PAmXD,6 Brabender plastograph mixing torque (30 rpm, 265 ± 5°C) is linearly related to Mn in a log/log diagram. © 1996 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
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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.
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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. 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.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 917-925 
    ISSN: 0887-624X
    Keywords: polymer blend ; phase inversion ; compatibilization ; PP-g-MA ; PAmXD,6 ; Brabender torque ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work deals with the study of the phase inversion phenomenon in blends of poly(m-xylylene adipamide) and maleic anhydride functionalized polypropylene (PAmXD,6/PP-g-MA blends) processed in a Brabender plastograph at 265 ± 5°C and 45 rpm. The viscosity of the components has been modelized by the Brabender torque and the phase inversion composition was determined by means of a solvent dispersion technique (SDT). The compatibilization, i.e., the amount of copolymer in the blend, does not modify the phase inversion location. The phase inversion composition is determined early during the process and is weakly or even not at all affected by further modification of viscosity ratio of the components versus mixing time. This work demonstrates that the only key parameter of the phase inversion composition is the viscosity ratio of the components at the first stage of the mixing process. An empirical equation linking volume fraction ratio for the phase inversion composition and the square root of the viscosity ratio of the components is proposed. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 917-925, 1997
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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