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  • Wiley-Blackwell  (19)
  • Institute of Physics  (9)
  • Oxford University Press  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 2799-2802 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 939-950 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron spin resonance (ESR) spectra of styrene/methacrylic acid copolymers neutralized with Cu(II) were observed at room temperature. Three magnetic species were detected; isolated Cu2+, Cu2+-Cu2+ pairs of Cu(II) acetate monohydrate type and anhydrous Cu(II) formate type. One of the absorption patterns due to the Cu2+-Cu2+ pair is the same as that of Cu(II) acetate monohydrate except linewidth. ESR data from the other species are summarized. ESR parameter, effect of the acid and Cu(II) contents, and spectral changes depending on sample preparation procedures or temperatures are discussed.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 435-444 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(dibenzyloxyphosphazene) (PBP), poly[bis(4-methylbenzyloxy)phosphazene] (PMBP) and poly[bis(4-chlorobenzyloxy)phosphazene] (PCIBP) were synthesized by reaction of poly(dichlorophosphazene) (PDCIP) and the corresponding sodium benzyl alkoxide. PDCIP was prepared by a ring-cleavage polymerization from hexachlorocyclotriphosphazene. The dielectric properties of the polymers were studied in the temperature range of 80 to 390 K at several frequencies between 0,1 and 100 kHz. Two relaxations, a relaxation above the glass transition temperature Tg and β relaxation below Tg, were observed in PBP and PMBP. The β relaxation was only observed in PCIBP. The a relaxations are related to a glass-rubber transition and the β relaxations to the local molecular motion of the short segments.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1057-1072 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric properties of poly(vinylidene fluoride) have been studied in the frequency range 10 Hz to 100 kHz at temperatures between -196 and 150°C. Three dielectric relaxations were observed: the α relaxation occurred near 130°C, the β near 0°C, and the γ near -30°C at 100 kHz. In the α relaxation the magnitude of loss peak and the relaxation times increased not only with increasing lamellar thickness, but also with decrease of crystal defects in the crystalline regions. In the light of the above results, the α relaxation was attributed to the molecular motion in the crystalline regions which was related to the lamellar thickness and crystal defects in the crystalline phase. In the β relaxation, the magnitude of the loss peak increased with the amount of amorphous material. The relaxation times were independent of the crystal structure and the degree of crystallinity, but increased slightly with orientation of the molecular chains by drawing. The β relaxation was ascribed to the micro-Brownian motions of main chains in the amorphous regions. The Arrhenius plots were of the so-called WLF type, and the “freezing point” of the molecular motion was about -80°C. The Cole-Cole distribution parameter of the relaxation time α increased almost linearly with decreasing temperature in the temperature range of the experiment. The γ relaxation was attributed to local molecular motions in the amorphous regions.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 753-758 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal properties by differential scanning calorimetry, stiffness, and melt flow rate (MFR) were measured for the complex transition-metal (Zn(II), Cu(II), Mn(II), and Co(II)) salts of ethylene-methacrylic acid copolymer (EMAA) with 1,3-bis(aminomethyl)-cyclohexane (BAC). It was found that the strength of both ionic interactions of metal cations with carboxyl groups and coordination bonds of amino groups to metals differ among metal species. In particular, the complex Mn salts are weaker than the complex salts of the other transition metals, which corresponds with Irving-Williams series of stability constants of transition metal-ion complexes. Stiffness depends predominantly on the degree of crystallinity of ionic crystallites in ionic clusters, which depends on the ionic species.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Temperature-dependent ESR spectra of Cu2+-Cu2+ pairs in ethylene/methacrylic acid copolymer neutralized with Cu(II) were reexamined in detail. The resonance positions and the linewidths of one of the ESR fine-structure lines showed thermal distension of the Cu2+-Cu2+ distance, and the slopes in the temperature variations changed at the temperature associated with melting of the polymer crystallites. No meaningful anomalies were observed around the temperature at which the preceding endothermic transition takes place. In this transition, the Cu2+-Cu2+ pairs seems to enter a disordered state, keeping almost the same paired structure. In contrast to this irreversible order-disorder transition, the melting process in the most part of the polyethylene crystallite phases starts to impose stress upon the Cu2+-Cu2+ pairs, accompanying the slope changes of the ESR parameters. These reversible variations with remarkable thermal hysteresis are compatible with the DSC analyses.
    Additional Material: 6 Ill.
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  • 7
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two new ethylene ionomers were synthesized, poly[ethylene-co-(5.4-mol-% 2-(4-carboxyphenoxy)ethyl methacrylate)] partially neutralized with Zn(II) (EMAA-BZnX), and poly[ethylene-co-(5.4 mol-% 2-(3-carboxypyridin-6-yloxy)ethyl methacrylate)] (EMAA-N) and its hydrochloride (EMAA-NHCl). Differential scanning calorimetric (DSC), X-ray diffraction, and dielectric and dynamic mechanical relaxation studies were made for the two ionomers to investigate the formation and structure of ionic aggregates. In EMAA-BZnX, DSC, dielectric and dynamic mechanical data suggest the formation of ionic aggregates in the neutralization range above 40%; X-ray diffraction data, however, did not show any ionic peak, while the ionic groups were not aggregated at all in EMAA-NHCl. From these results, the ion-aggregation in ionomers is discussed with respect to chemical structure and the nature of ionic groups.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 2647-2655 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This article describes dielectric properties of complex Zn(II) salts of ethylene-methacrylic acid copolymer (5.4 mol% methacrylic acid) with n-hexylamine. In all samples, the β′ relaxation near 340 K and γ relaxation near 170 K are observed. These are assigned, respectively, to micro-Brownian molecular motion of long segments above Tg and to local molecular motion of short segments below Tg. The dielectric results indicate that ionic clusters are not formed in these systems.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 3919-3927 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A spin-probing technique was first applied to a study of a non-magnetic ionomer, polyethylene/methacrylic acid copolymer neutralized with Zn2+ (E-MAA-Zn); 2 mol-% Cu2+ ions were incorporated in replacement of Zn2+, and its ESR spectra were observed in detail at various temperatures in order to obtain physico-chemical properties of E-MAA-Zn, especially its structural changes. We found no significant influence of the 2 mol-% Cu2+ -incorporation upon the properties of the Zn2+ ionomer by differential scanning calorimetry (DSC), which showed two endothermic peaks, (1) an irreversible one at lower temperature which is associated with the ionic aggregate phase in the ionomer, (2) a reversible one at higher temperature with considerable thermal hysteresis which is due to melting of the polymer main chains. ESR hyperfine coupling constants (A∥ and A⊥) of Cu2+ showed no sign of structural changes of the polymer around the phase-transition temperatures, whereas ESR g-values (g∥ and g⊥) of Cu2+ proved the onset of the softening of the polymers to be attributable to polymer melting. The latter slope-changes in the temperature dependences were reversible, although with considerable thermal hysteresis. These findings are compatible with the DSC data. As for the irreversibility regarding the endotherm at lower temperature, broad ESR hyperfine components recovered gradually, indicating an order-disorder nature of the ionic aggregate phase transition.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 351-362 
    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: Thermal properties by DSC, stiffness, melt viscosity, tensile properties, and dynamic mechanical properties were measured for the Na+, K+, Mg2+, Zn2+, Cu2+, Mn2+, and Co2+ salts of poly(ethylene-co-methacrylic acid) (EMAA). The changes in the structure and properties with increasing neutralization are larger in the alkaline and alkaline earth metal salts than in the transition metal salts. The stiffness shows a maximum at 33% neutralization in both the alkaline and alkaline earth metal salts, while no maxima are found up to 60% neutralization in the transition metal salts. The microphase separation of salt group aggregates is observed in both the alkaline and alkaline earth metal salts, but is not seen in the transition metal salts. These differences were attributed to both the stronger ionic interactions and the larger number of carboxyl groups associated with the alkaline and alkaline earth metal salts in the ordered structure of ionic salt groups (ionic crystallites). The mechanical properties measured at low strain, such as stiffness and yield stress, strongly depend on the degree of the crystalline order of the ionic crystallites. The high-strain properties, such as tensile strength and elongation at break, depend on the strength of the ionic interactions and the valence of the cation.
    Additional Material: 13 Ill.
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