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  • Polymer and Materials Science  (31)
  • TMDSC  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 276 (1998), S. 289-296 
    ISSN: 1435-1536
    Keywords: Key words Semicrystalline polymer ; PEEK ; TMDSC ; DMA ; melting ; crystallization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  Temperature-modulated DSC (TMDSC) and dynamic-mechanical analysis (DMA) allows the study of degree of crystallinity changes of polymers. From the comparison of the two methods using the same temperature–time program, one expects additional information about the processes occurring in the melting region. A first description of temperature-modulated DMA is given. The effect of reversible melting during every period of temperature modulation has been observed in the melting region of PEEK. The number of molecules which undergo reversible melting for a given quasi-isotherm decreases with time. At 600 K the fraction of the material involved in this process during one modulation cycle is between 0.35% and 0.25%, but has a non-zero value at infinity. The kinetics of this decrease indicates that the process of the structural changes is most likely related to the melt. It can be explained considering an entanglement of the disentangled melt surrounding the just molten crystals. The results are in agreement with the four-state scheme for polymer crystallization and melting proposed by Strobl.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 60 (2000), S. 807-820 
    ISSN: 1572-8943
    Keywords: calorimetry ; crystallization ; PCL ; PEEK ; PEN ; PET ; polymer ; temperature modulation ; TMDMA ; TMDSC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Quasi-isothermal temperature modulated DSC and DMA measurements (TMDSC and TMDMA, respectively) were performed to determine heat capacity and shear modulus as a function of time during crystallization. Non-reversible and reversible phenomena in the crystallization region of polymers can be observed. The combination of TMDSC and TMDMA yields new information about local processes at the surface of polymer crystals, like reversible melting. Reversible melting can be observed in complex heat capacity and in the amplitude of shear modulus in response to temperature perturbation. The fraction of material involved in reversible melting, which is established during main crystallization, keeps constant during secondary crystallization for PCL PET and PEEK. This shows that also after long crystallization times the surfaces of the individual polymer crystallites are in equilibrium with the surrounding melt. Simply speaking, polymer crystals are ‘living crystals’.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 61 (2000), S. 649-659 
    ISSN: 1572-8943
    Keywords: complex heat capacity ; non-linearity ; non-linear thermal response ; non-stationarity ; reversing heat capacity ; TMDSC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract To treat data from temperature modulated differential scanning calorimetry (TMDSC) in terms of complex or reversing heat capacity firstly one should pay attention that the response is linear and stationary because this is a prerequisite for data evaluation. The reason for non-linear and non-stationary thermal response is discussed and its influence on complex (reversing) heat capacity determination is shown. The criterion for linear and stationary response is proposed. This allows to choose correct experimental conditions for any complex heat capacity measurement. In the case when these conditions can not be fulfilled because of experimental restrictions one can estimate the influence of non-linearity and non-stationarity on measured value of complex or reversing heat capacity.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 59 (2000), S. 279-288 
    ISSN: 1572-8943
    Keywords: AC calorimetry ; crystallization ; PCL ; polymer ; temperature modulation ; TMDSC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Quasi-isothermal temperature modulated DSC (TMDSC) were performed during crystallization to determine heat capacity as function of time and frequency. Non-reversible and reversible phenomena in the crystallization region of polymers were distinguished. TMDSC yields new information about the dynamics of local processes at the surface of polymer crystals, like reversible melting. The fraction of material involved in reversible melting, which is established during main crystallization, keeps constant during secondary crystallization for polycaprolactone (PCL). This shows that also after long crystallization times the surfaces of the individual crystallites are in equilibrium with the surrounding melt. Simply speaking, polymer crystals are ‘living crystals’. A strong frequency dependence of complex heat capacity can be observed during and after crystallization of polymers.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 160 (1988), S. 131-140 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: For a polymer system sulfur-styrene containing 10 wt.-% styrene the morphologie depending on the polymerization temperature and time is described. Besides the characteristical orthorhombic phase a monoclinic and a pseudoorthorhombic phase were detected. Moreover amorphous material exists, depending on the polymerisation parameters.
    Notes: Für ein Polymersystem Schwefel-Styrol mit 10% Styrol wird die Abhängigkeit der Morphologie von der Polymerisationstemperatur und -zeit beschrieben. Neben der charakteristischen orthorhombischen Phase wurden röntgenographisch eine monokline und eine pseudoorthorhombische Phase nachgewiesen. Außerdem liegt, abhängig von den Polymerisationsparametern, ein amorpher Anteil vor.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 25 (1957), S. 465-478 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The monomer structure of several linear high polymers in monolayers has been studied with an automatic recording film balance and surface potentiometer of very high precision. The method is based on the resolution of the monomer structure from estimation of the limiting areas of the force - area and surface - potential area curves. The structures of poly(vinyl acetate), poly(vinyl alcohol), poly(methyl methacrylate), poly-(methacrylonitrile), and ethoxylin polymer have been determined. In addition the secondary cohesion, which corresponds to its three-dimensional equivalent, was related to the stability of the polymer film. It was found in the vinyl polymer series that secondary cohesion decreased in the order poly(vinyl alcohol), poly(methacrylonitrile), poly(methyl methacrylate), poly(methyl acrylate) to poly(vinyl acetate). Alternatively a comparison of specific areas at A/W and O/W interfaces renders conclusion on the rigidity of a polymer. Whereas poly(vinyl acetate) showed identical areas at both interfaces, poly(methyl methacrylate) spread to larger areas at the O/W interface. From this it is evident that the α-methyl group in the vinyl chain exerted strong cohesive forces. This effect was even more pronounced with the ethoxylin resin with two benzene rings in the monomer unit. Application of a statistical mechanical equation for the two-dimensional behavior of linear polymer indicated also that whereas poly-(vinyl acetate) is a flexible chain, ethoxylin polymer is a rigid chain.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 1 (1980), S. 407-409 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 16 (1978), S. 153-154 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Undrawn poly(ethylene terephthalate) was crystallized using several temperature programmes to get samples of different crystalline structure, as indicated by varying thickness of the amorphous layer between neighbouring lamellae. The glass transition is influenced by the thickness of these layers. A broadening of the relaxation spectrum at lower frequencies occurs due to thinner amorphous layers. This influence can be understood within the concept of “hindered glass transition”.
    Notes: An unterschiedlich kristallisiertem Poly(ethylenterephthalat), bei dem insbesondere die Schichtdicke der amorphen Bereiche zwischen benachbarten Lamellen variiert wurde, erfolgte die Untersuchung des thermischen Glasübergangs. Die Schichtdicke beeinflußt maßgeblich die For des Glasübergangs. Eine Verringerung der Schichtdicke bewirkt eine Verbreiterung des niederfrequenten Teils des Spektrums der Relaxationszeiten. Diese Beeinflussung ist im Rahmen des Konzepts des „behinderten Glasübergangs“ zu verstehen.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 21 (1983), S. 680-682 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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