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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 849-856 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 3855-3859 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The heat capacities of 38 semicrystalline poly(oxymethylene)s and poly(oxyethylene)s were determined by differential scanning calorimetry from 205 K through the melting transition. By comparison with the well known limiting heat capacities of the supercooled liquids and the crystals of the macromolecules it was found that there are negative and positive deviations from additivity of the heat capacities with crystallinity between the glass transition and the melting transition. The negative deviations are linked with “rigid amorphous” material, and the positive deviations were previously linked to defect formation or early melting. The rigid amorphous fraction in poly(oxymethylene) is constant up to the melting region, in contrast to polypropylene, where it is decreasing with temperature. The proposed mesophase transition in poly(oxymethylene) is shown to be a minor effect. The poly(oxyethylene) heat capacity is governed by positive heat capacity deviations within the rather short temperature range between glass transition and melting.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 141-150 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transitions of poly(oxy-2,2′-dimethylazoxybenzene-4,4′-diyloxydodecanedioyl) (PDAD) have been analyzed by differential scanning calorimetry, optical microscopy, and light scattering. The mesophase glass devitrifies at 288 K [ΔCp = 220 J/K mol]. Crystallization from the liquid mesophase can be described between 322 and 362 K by an Avrami expression with an exponent between 3 and 4. Results of light scattering and optical microscopy are in accord with a spherulitic morphology grown after athermal nucleation. Melting of the semicrystalline samples (crystallinity up to 58%) occurs at about 391 K. The heat of fusion of the completely crystalline sample is calculated to be only 13.55 kJ/mol. The mesophase to isotropic phase transition occurs at 418 K with a heat of transition of 4.1 kJ/mol. A general discussion of these transitions is given.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 1323-1330 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When poly(oxymethylene) is doped with increasing amounts of low molecular weight poly(oxyethylene), a stepwise disappearance of the boundaries between the spherulites is observed. At a poly(oxyethylene) content of 5 wt.-%, the replica of a bulk sample viewed in an electron microscope seems to have only centers of spherulites and slightly marked boundaries between them. A more careful examination of the replica shows that this effect is due to strong interpenetration of the lamellae of the adjacent spherulities of poly(oxymethylene). It is well known that the mechanical properties of many two-component systems are improved by adding small amounts of a second component. On the basis of our observations it is possible to correlate the interpenetration of spherulites with the improvement of some mechanical properties of bulk samples. Interpenetration is possible when two “hollow” dendritic spherulites are brought into contact. Such a change of the spherulite structure by an additive is due to a rejection of the additive into interlamellar regions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 3 (1992), S. 51-59 
    ISSN: 1042-7147
    Keywords: Thermal analysis ; Heat capacity ; Rigid amorphous ; Glass transition ; Poly(pivalolactone) ; 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
    Notes: Quantitative thermal analysis was carried out for poly-(pivalolactone) (PPVL), including heat capacity determinations from 140 to 550 K. The experimental Cp below the glass transition temperature was fitted to an approximate vibrational spectrum and the ATHAS computation scheme was used to compute the “vibration only” heat capacities from 0.1 to 1000 K. The liquid Cp was derived from an empirical addition scheme and found to agree with the experimental Cp with an RMS of ±2.8% from 240 K to 550 K. A glass transition, Tg, could be detected at 260 K, and the change in heat capacity for 100% amorphous PPVL was calculated to be 38.8 J/(K mol). Above Tg, semicrystalline samples seem to show a rigid amorphous fraction that does not contribute to the increase in heat capacity at Tg. Using the ATHAS recommended heat capacities, the various thermodynamic functions (enthalpy, entropy, and Gibbs function) were derived. The residual entropy at 0 K for the amorphous PPVL was calculated to be 5.2 J/(K mol) per mobile bead, and was comparable to that obtained for a series of linear, aliphatic polyesters analyzed earlier.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 69-77 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Polypivalolactone (PPVL) is a highly crystalline polyester formed either by nucleophilic or electrophilic ring-opening polymerization of 2,2-dimethyl-β-propiolactone, commonly known as pivalolactone (PVL). The thermal properties and crystallization kinetics of the polymer formed under reaction injection molding (RIM) conditions were studied. The crystallization kinetics of PPVL were measured using differential scanning calorimetry (DSC), and Avrami theory was used to interpret the bulk crystallization kinetics. A comparison was made with commercially prepared PPVL. The kinetics data indicate laboratory prepared PPVL, which is of lower molecular weight, has similar crystallization rates compared to the higher molecular weight commercial material. The kinetics data also indicate the rate of crystallization is relatively rapid overall for PPVL, with low activation energies of crystallization. The calorimetric studies also utilized DSC and simultaneous ther-mogravimetric analysis/differential scanning calorimetry (TGA/DSC). Thermal analysis showed a clear difference in melting behavior between high and low molecular weight material, possibly a reflection of the presence of the α and γ-crystal forms of the polymer.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 675-685 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of condis (conformationally disordered) crystal formation from the melt and of rigid crystals from condis crystals has been studied by differential scanning calorimetry for trans-1,4-polybutadiene and polytetrafluoroethylene. Generally very low two-stage Avrami exponents between 0.02 and 1.74 were needed to describe the fast and often incomplete crystallizations. None of the commonly accepted crystal nucleation and growth models seems to fit the data.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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