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  • 1
    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
    Amsterdam : Elsevier
    Thermochimica Acta 228 (1993), S. 47-60 
    ISSN: 0040-6031
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 37 (1991), S. 1751-1758 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung VitrifikationphÄnomeme und strukturelle Relaxations-respektive AlterungsvorgÄnge von Epoxiden wurden mitells isothermer DSC Messungen untersucht. Die Vitrifikationszeit, der Grenzwert des Unwandlungsgrades und die Grenztemperatur der Glasumwandlung wurden in Bereich von 30 bis 100
    Notes: Abstract Vitrification phenomena and further structural relaxation processes or physical ageing occurring in the isothermal curing reaction of an epoxy resin are studied by Differential Scanning Calorimetry (DSC). The vitrification time,t v , the limiting conversion degree and the limiting glass transition temperature (T g) are evaluated at curing temperatures (T c) between 30 and 100
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 47 (1996), S. 103-115 
    ISSN: 1572-8943
    Keywords: glass transition ; MDSC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The modulated differential scanning calorimetry (MDSC) technique superimposes upon the conventional DSC heating rate a sinusoidally varying modulation. The result of this modulation of the heating rate is a periodically varying heat flow, which can be analysed in various ways. In particular, MDSC yields two components (‘reversing’ and ‘non reversing’) of the heat flow, and a phase angle. These each show a characteristic behaviour in the glass transition region, but their interpretation has hitherto been unclear. The present work clarifies this situation by a theoretical analysis of the technique of MDSC, which introduces a kinetic response of the glass in the transition region. This analysis is able to describe all the usual features observed by MDSC in the glass transition region. In addition, the model is also able to predict the effects of the modulation variables, and some of these are discussed briefly.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 49 (1997), S. 79-85 
    ISSN: 1572-8943
    Keywords: cross-linking degree ; DSC ; enthalpy relaxation ; epoxy resins ; physical aging ; reactive diluent
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Structural relaxation in different epoxy-anhydride and epoxy-diamine resins has been investigated by differential scanning calorimetry using annealing and cooling rate experiments. The annealing experiments lead to the determination of enthalpy loss,δH, at an equivalent annealing temperatureT a=T g-20, and for periods of annealing time, ta, between 1 h and 4 months. The variation ofδH with logta, defines a relaxation rate per decade,rrpd, which is very sensitive to changes of the epoxy network. The cooling rate experiments allow the determination of the apparent activation energy,δh *. The effect of the degree of crosslinking, the addition of a reactive diluent, which acts as flexibilizer, and the length of cross-link onrrpd and δh* was studied.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 59 (2000), S. 289-303 
    ISSN: 1572-8943
    Keywords: epoxy resins ; glass transition ; thermosets ; TMDSC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The glass transition temperature of thermosets is determined by alternating differential scanning calorimetry (ADSC), which is a temperature modulated DSC technique. The different values of the glass transition obtained from heat flow measurements (total and reversible) and heat capacity (modulus of the complex heat capacity) are analysed and compared with the values obtained by conventional DSC. The effect of the sample mass on the values of Tg, heat capacity and phase angle has been analysed. The effect of the thermal contact between sample and pan has been studied using samples cured directly inside the pan and disc-shaped samples of different thickness. The results obtained for the thermal properties and the phase angle are compared and analysed. The modulus of the complex heat capacity enables the determination of the dynamic glass transition, Tgα, which is frequency dependent. The apparent activation energy ofthe relaxation process associated with the glass transition has been evaluated from the dependence of Tgα on the period of the modulation.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 49 (1997), S. 693-702 
    ISSN: 1572-8943
    Keywords: DSC ; helical conformation ; poly(α-n-alkyl-L-aspartate)s
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A series of poly(α-n-alkyl β-L-aspartate)s (n being the number of carbon atoms in the linear alkyl side chain, withn=1, 2, 4, 6, 8, 12, 18 and 22), was studied by differential scanning calorimetry and thermogravimetric analysis. The effect of the length of the alkyl group on thermal properties such as stability, melting and crystallization of side chains, was investigated. For the polymers with n≥12, two endothermic peaks at T1 and T2 were detected separating three distinct phases A, B and C. The peak at T1 corresponds to the melting of the crystallized paraffinic side chains (transition A-B), and the peak: at T2 may be attributed to a transition (B-C), implying a liquid crystal phase.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 12 (1984), S. 173-180 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The glass transition temperature of amorphous and fractionated poly(ethylene terephthalate) has been measured by differential scanning calorimetry. The application of the Fox-Flory equation for the range of molecular weights between 37100 and 4500 gives the values of Tg∞=342.4 K and Kg=51200. The low value of Kg is interpreted by the free volume theory. The flex energy of the chain is evaluated by the Gibbs-Di Marzio theory with a value of 1483 cal/mol. These results are compared with those obtained by other authors for the poly(ethylene adipate) and the poly(diethylene terephthalate).
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 113-126 
    ISSN: 0887-6266
    Keywords: enthalpy relaxation ; physical aging ; DSC ; glassy state ; thermoplastic polymers ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The enthalpy relaxation of a series of linear amorphous polyesters (poly(propylene isophthalate) (PPIP), poly(propylene terephthalate) (PPTP), poly(ethylene terephthalate) (PETP), and poly(dipropylene terephthalate) (PDPT)) has been investigated by differential scanning calorimetry (DSC). These polyesters have been annealed at equal undercooling below their respective glass transition temperatures, Tg, (Tg - 27°C, Tg - 15°C, and Tg - 9°C) for periods of time from 15 min to 480 h. The key parameters of structural relaxation, namely the apparent activation energy (Δh*), the nonlinearity parameter (x) and the nonexponentiality parameter (β), have been determined for each polyester and related to an effective relaxation rate (1/τeff) and to the chemical structure. We observe that the variation of the structural relaxation parameters shows a trend that is common to other polymeric systems, whereby an increase of x and β corresponds a decrease in Δh*. The comparison of these parameters in PETP and in PPTP gives information about the effect of the introduction of a methyl group pendant from the main chain; the x parameter increases (i.e., a reduced contribution of the structure to the relaxation times), β increases (i.e., a narrow distribution of relaxation times), and Δh* decreases. Additionally, enthalpy relaxation experiments show that a decrease of Δh* correlates with an increase of 1/τeff, when they are measured at a fixed value of the excess enthalpy, δH. The introduction of an isopropyl ether group in PDPT with respect to PPTP decreases both x and β, but increases Δh*, which the rate of relaxation decreases. The ring substitution in PPTP and PPIP originates less significant changes in the structural parameters. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 113-126, 1998
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 509-522 
    ISSN: 0887-6266
    Keywords: physical aging ; enthalpy relaxation ; epoxy resins ; thermosets ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The physical aging of an epoxy resin based on diglycidyl ether of bisphenol-A cured by a hardener derived from phthalic anhydride has been studied by differential scanning calorimetry. The isothermal curing of the epoxy resin was carried out in one step at 130°C for 8 h, obtaining a fully cured resin whose glass transition was at 98.9°C. Samples were aged at temperatures between 50 and 100°C for periods of time from 15 min to a maximum of 1680 h. The extent of physical aging has been measured by the area of the endothermic peak which appears below and within the glass transition region. The enthalpy relaxation was found to increase gradually with aging time to a limiting value where structural equilibrium is reached. However, this structural equilibrium was reached experimentally only at an aging temperature of Tg-10°C. The kinetics of enthalpy relaxation was analysed in terms of the effective relaxation time τeff. The rate of relaxation of the system given by 1/τeff decreases as the system approaches equilibrium, as the enthalpy relaxation tends to its limiting value. Single phenomenological approaches were applied to enthalpy relaxation data. Assuming a separate dependence of temperature and structure on τ, three characteristic parameters of the enthalpic relaxation process were obtained (In A = -333, EH = 1020 kJ/mol, C = 2.1 g/J). Comparisons with experimental data show some discrepancies at aging temperatures of 50 and 60°C, where sub-Tg peaks appears. These discrepancies probably arise from the fact that the model assumes a single relaxation time. A better fit to aging data was obtained when a Williams-Watts function was applied. The values of the nonexponential parameter β were slightly dependent on temperature, and the characteristic time was found to decrease with temperature. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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