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
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 84 (1980), S. 1944-1950 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 65-74 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diglycidyl ether of bisphenol-A, an uncured epoxy resin, has been studied by pulsed NMR. Values of the proton relaxation times T1, T1p, and T2 have been measured over the temperature range from -160 to 200°C. The resin was studied in its monomeric form and in two mixtures containing higher oligomers. The relaxation times are interpreted in terms of the molecular motion in the resins. The motion responsible for relaxation in the solid monomer form is thought to be methyl group reorientation at low temperatures and general molecular motion at high temperatures. The motions are characterized by activation energies of 5 kcal/mole and 33 kcal/mole, respectively. The solid mixtures exhibit similar effects to the monomer, but an additional relaxation mechanism is observed which is attributed to segmental motion. This motion is characterized by an activation energy of 12-15 kcal/mole. The self-diffusion coefficient was measured in the liquid monomer, and the activation energy for self-diffusion is found to be 11 kcal/mole.
    Additional Material: 4 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
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1453-1459 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The curing process, during which the monomeric diglycidyl ether of bisphenol-A is cured with 4,4′-methylenedianiline, has been studied by pulsed NMR. Values of the proton relaxation times T1, T1ρ, and T2 have been measured as a function of time as the resin system cures at constant temperature. The relaxation times are interpreted in terms of the decrease in general molecular motion which results from the cure. Plots of correlation frequency versus time for the constant-temperature cure were constructed for three temperatures. It is shown that these three plots can be represented by a reduced curve. With certain simplifying assumptions, the shape of this reduced curve. With certain simplifying assumptions, the shape of this reduced curve can be accounted for in terms of the chemical rate constant and an exponent relating molecular weight to viscosity. The activation energy for the cure is estimated to be 11.7 kcal/mole.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 449-456 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The monomeric diglycidyl ether of bisphenol-A cured with methylenedianiline has been studied by pulsed NMR. Values of the proton relaxation times T1, T1p, and T2 have been measured over the temperature range -160 to 200°C. The system was studied after being fully postcured at 180°C and after being cured at 100°C and at 54°C. The relaxation times are interpreted in terms of molecular motion in the cured resins, i.e., methyl group reorientation, segmental motions, and general molecular motion. The results are compared with those obtained previously by us for the uncured resin. Correlation frequencies for the segmental motions are compared with those obtained from dielectric relaxation and mechanical loss studies. There are at least two principal segmental motions present in the cured system, and the nature of these motions is found to depend on the cure temperature. These effects are discussed in terms of crosslinking and annealing of the system.
    Additional Material: 4 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
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 118-121 
    ISSN: 0749-1581
    Keywords: 13C CP/MAS NMR ; Solid-state phenyl group rotation ; T1ρ ; Lineshape 2D EXSY ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A combination of solid-state 13C CP/MAS NMR methods was used to study the rates of rotation of the phenyl group in 3,5-dimethyl-1-phenylhex-1-yn-3-ol. The methods used were T1ρ measurements, lineshape analysis and 2D exchange spectroscopy over the temperature range 219-284 K. The rates of rotation obtained from the lineshape and 2D EXSY methods give an energy of activation of 58.6 ± 3.0 kJ mol-1. In good agreement with this, the T1ρ measurements give an activation energy for the rotation of 58.7 ± 3.6 kJ mol-1. The two sets of data are shown to be compatible, within experimental error, with a calculated value for the dipolar carbon-hydrogen interaction (B) from an assumed molecular geometry.
    Additional Material: 3 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...