Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 437-449 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric permittivity and loss of diglycidyl ether of bisphenol-A-based thermosets cured with diaminodiphenyl methane and diaminodiphenyl sulfone have been measured over a temperature range 77-400 K after curing or aging for a predetermined duration. Of the two sub-Tg relaxations, the height of the γ relaxation peak monotonically decreases during both the cure and postcure periods, and the height of the β relaxation peak first increases to a maximum value and then decreases. This decrease is attributed to physical aging effects. The height of the α-relaxation peak decreases. The γ- and β-relaxation peaks become increasingly separated in temperature. A concept of accumulated equivalent curing time which is based upon known chemical kinetics has been introduced for use in both theoretical and practical aspects of the study of thermosets. It is shown that substantial curing of the sample occurs during its slow heating to the curing temperature. The use of this concept in the curing of thermosets is illustrated. A procedure for the analysis of the distribution of relaxation times from a set of results limited in both frequency and temperature range is described. The distribution parameter is 0.20 and 0.16 for the γ and β process, respectively, and remains constant with postcuring and physical aging. The distribution parameter for the α process decreases from 0.60 to 0.36 on curing.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 723-730 
    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 sol-gel-glass transformations have been studied in the thermosets of diglycidyl ether of bisphenol A cured with diamino diphenyl methane and diamino diphenyl sulfone, at different temperatures using Brillouin light scattering. The Shape of the Brillouin peak is generally broad. This is attributed to the damping of elastic waves in the mixture of unpolymerized low-molecular weight fluid and the polymer chains forming the networks. The Brillouin peak becomes sharp and narrow at complete curing of the thermosets. The phonon velocity increases and the attenuation decreases with the curing time. These changes occur in two steps with the second step appearing near the gelling time of the thermosets. A semilogarithmic plot of the time for the velocity and attenuation to reach half of their total change against the reciprocal temperature yields a straight line with different slopes for the two thermosets. It is suggested that Brillouin light scattering is a useful non-destructive, in-line, method for control in the processing of epoxy thermosets.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 433-443 
    ISSN: 0887-6266
    Keywords: epoxide-based thermosets ; dielectric effects during curing of epoxide-based thermosets ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric permittivity ε′ and loss ε″ of diglycidyl ether of bisphenol-A thermosets cured with nonstoichiometric amounts of diamino-diphenyl methane have been measured during the course of their chemical reactions from the sol to gel to glass-formation regions. ε′ monotonically decreases with time and ε″ initially decreases, increases to a peak value, and finally decreases to extremely low values characteristic of the glassy state. The initial decrease in ε″ is due to the decrease in the dc conductivity, and the peak is due to the dipolar reorientation. The appearance of these features shifts to longer time when the thermoset is stoichiometrically starved by decreasing the amount of the curing agent and, at a molar ratio of 4 : 1 of the epoxide to diamine, the ε″ peak does not appear during the curing process. Complex plane plots of ε′ and ε″ have the shape of an arc in all cases except when the molar ratio of the epoxide to diamine is 4 : 1. The dielectric consequences of the chemical changes with time during the crosslinking of a thermoset are analogous to the frequency dependence of ε″ of a condensed phase. The time dependence of ε″ follows a stretched exponential decay, φ(t = exp - [(t/τ)γ], where 0 〈 γ 〈 1. The parameter decreases with decreasing amine content. ε″ has been analyzed to obtain the increase in the relaxation time as curing progresses. A representation of ε* in terms of electrical modulus M* shows the occurrence of, first a Maxwell relaxation due to dc conductivity, and second a dipolar relaxation, during the period of a typical isothermal cure. Changes in the features of the isothermal cure that occur on changing the amount of the curing agent are discussed in terms of network formation in the thermoset, and the change in the electrical conductivity with curing time has been analyzed in terms of both a power law for gel formation and by a new equation that suggests an approach toward a singularity.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 445-453 
    ISSN: 0887-6266
    Keywords: epoxide-based thermosets, sub-Tg relaxations during post-cure and aging of ; dielectric properties in post-cure and aging of epoxide-based thermosets ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric permittivity and loss of diglycidyl ether of bisphenol-A (DGEBA) cured with greater than and less than the stoichiometric amounts of diaminodiphenyl methane (DDM) have been measured over a temperature range 77-350 K prior to curing and gelation, after curing at about 340 K and further aging for a predetermined period. The height of the γ-relaxation peak monotonically decreases during the post-cure period and becomes masked by the contributions from the β-relaxation peak, whose height, in turn, first increases on postcuring to a same maximum value for both nonstoichiometric thermosets and then decreases. This decrease is attributed to physical aging effects. The β-relaxation peak shifts towards higher temperature on postcuring. Comparison between the changes in the dielectric properties of the saturated and starved thermosets show that while the γ-relaxation process may be attributed to the motion of the epoxide dipolar groups of the unreacted DGEBA, the β-relaxation process is not attributable entirely to the motion of —OH groups and of the unreacted amines in the thermoset. Explanations involving the chain and network packing in the structure of a thermoset are necessary for the observed behavior of the β-relaxation process in amine saturated and starved thermosets.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sub-Tg relaxations of bisphenol-A-based thermosets cured with diaminodiphenyl methane and diaminodiphenyl sulfone have been studied by dielectric measurements over the frequency range 12 Hz to 200 kHz from their ungelled or “least” cured states to their fully cured states. Both thermosets show two relaxation processes, γ and β, as the temperature is increased toward their Tgs. In the ungelled states, the γ process is more prominent than the β process. As curing proceeds, the strength of the γ process decreases and reaches a limiting value, while that of the β process initially increases, reaches a maximum value, and then decreases. An increase in the chain iength and the number of crosslinks increases the number of -OH dipoles and/or degree of their motions in local regions of the network matrix. This is partly caused by the decreasing efficiency of segmental packing as the curing proceeds. The sub-Tg relaxations become increasingly more, separated from the α relaxation during curing. Physical aging causes a decrease in the strength of the β relaxation of the thermosets as a result of the collapse of loosely packed regions of low cross-linking density, and this decrease competes against an increase caused by further crosslinking during the “post-cure” process.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 1621-1639 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric permittivity ∊′ and loss ∊″ during the crosslinking or curing of diglycidyl ether of bisphenol-A with diaminodiphenyl methane and diaminodiphenyl sulfone have been measured from the sol to gel to glass-formation regions. The ∊′ monotonically decreases with time and the ∊″ initially decreases, then increases to a peak value and finally reaches extremely low values characteristic of the glassy state. These features shift to shorter times with an increase in the temperature of curing. Complex-plane plots of ∊′ and ∊″ have the shape of an are skewed at both the short-time and the long-time intercepts and resemble Cole-Cole plots of ∊*. Thus the dielectric consequences of the chemical changes with time during the cross-linking of a thermoset are analogous to the frequency dependence of ∊* in an amorphous solid. The time dependence of ∊* follows a stretched exponential decay, φ(t) = exp [- (t/τ)γ] where 0 〈 γ 〈 1. The parameter γ is in the range 0.2 to 0.4, and increases with a decrease in the curing temperature. Additional curing at longer times produces polymer segments in the network with a high reorientation rate. This is observed as deviations from the shape of a skewed arc at the limiting long-time intercept and appears as a secondary relaxation during the curing process, but at very long times. The ∊′ and ∊″ have been analyzed and the roles of dc conductivity, Δ∊, and γ in determining the shape of the curing isotherms have been estimated. A representation of the data in the complex electrical modulus, M*, formalism shows the occurrence of two relaxation processes during the period of a typical isothermal cure. The feature observed at the shortest time is due to conductivity relaxation and the subsequent feature is due to the dipolar relaxation processes during the curing. The time of cure at which the relaxation rate reaches a fixed value follows an exponential relation with the reciprocal curing temperature with parameters which are characteristic of a thermoset. The decrease in dc conductivity during sol → gel conversion follows the scaling law used in the description of a critical phenomenon.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...