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
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 195-204 
    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: Die kinetischen Parameter der Polymerisation eines Epoxidharzes, gekennzeichnet durch hohe Enthalpie und niedrige Wärmeleitfähigkeit, wurden durch DSC-Messungen bestimmt. Aus den Peakmaximum-Methoden (Kissinger, Ozawa und Lam) wurde für die Aktivierungsenergie Ea ein Mittelwert von 62,71 kJ · mol-1 erhalten; die Achar-brindley-Sharp-Methode, die ein homogenes Gesetz und die Probentemperatur verwendet, ergab 68 kJ · Mol-1. Die Meßergebnisse wurden mit theoretischen Berechnungen (aus einer Modellierung des Temperaturprofils in der DSC-Meßzelle während des Härtens) verglichen. Der Anstieg der scheinbaren kinetischen Parameter mit der Heizgeschwindigkeit V (ausgedrückt durch einen Parameter e = ΔEa/ΔV) resultiert aus Meßungenauigkeiten der Temperatur, verursacht durch die exotherme Reaktion. Wird anstelle der programmierten Kalorimetertemperatur die tatsächlich gemessene Temperatur berücksictigt, nimmt e von 1,725 auf 0,613 ab.
    Notes: Kinetic parameters of the polymerization of an epoxy resin, characterized by a high enthalpy and a low heat conductivity, are determined by DSC analysis. The mean value obtained from the peak maximum evolution methods (Kissinger, Ozawa and Lam) for the activation energy Ea was 62.71 kJ · mol-1; the Achar-Brindley-Sharp method, using the homogeneous law and the sample temperature, led to 68 kJ · mol-1. A comparison between theoretical computations (obtained from a modeling of the temperature profile in the DSC crucible during cure) and measurements is given. The increase of the apparent kinetic parameters with the heating rate V (expressed with a parameter e = ΔEa/ΔV) essentially results from the overestimation of the temperature, induced by the exothermicity of the phenomenon. A decrease of e from 1.725 to 0.613 is observed, with the measured temperature instead of the set calorimeter temperature.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Various complexes of boron trifluoride and typical organo-phosphours compounds have been investigated using proton and fluorine resonance (at variable temperature) and boron and phosphorus resonance. In BF3, boron resonance is insensitive to the complex strength, but fluorine resonance suggests the possibility of various types of complexes on the phosphorus group or, additionally on the heteroatoms (e.g. oxygen, nitrogen) of the molecule. These complexes are probably σ type. Proton chemical shifts in the organo-phosphorus compounds follow the same trends as in similar complexes of amines, esters etc.; these perturbations may be mainly due to magnetic anisotropy effects; proton-phosphorus couplings conversely follow changes in phosphorus electronegativity.
    Notes: On a étudié, en résonance du proton et du fluor (à température variable) ainsi qu'en résonance du bore et du phosphore, un certain nombre de complexes entre BF3 et des composés organo-phosphorés typiques. En ce qui concerne BF3, la résonance de bore reste insensible à la force du complexe; par contre, la résonance du fluor suggéère l'existence de plusieurs types de complexes, soit sur le groupe phosphoré, soit sur les hétéroatomes (par example N, O) de la molécule. Ces complexes sont vraisemblablement de type σ pur. Le déplacement chimique des protons dans la molécule organo-phosphorée subit sensiblement les mêmes perturbations que dans les autres molécules complexables (amines, esters, etc.); ces perturbations peuvent provenir avant tout d'effets d'anisotropie magnétiques; par contre, les couplages proton-phophore suivent la modification de l'électronégativité de ce dernier.
    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...