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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 50 (1978), S. 976-979 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 50 (1978), S. 1212-1218 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 17 (1978), S. 654-662 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zusammenfassung Die GlasübergangstemperaturenT g von Asphaltproben verschiedener Herkunft und Penetrationsgrade wurden mit einem Differentialkalorimeter (DSC-2) bestimmt. DieT g -Werte von Proben aus zwei Quellen nahmen mit wachsendem Penetrationsgrad ab, wohingegen diese bei Proben aus einer dritten Quelle bei allen Penetrationsgraden gleich blieben. Durch Einsetzen dieserT g -Daten in die Williams-Landel-Ferry-Gleichung wurden sowohl unter Verwendung von universellen als auch von optimierten Werten der KonstantenC 1 undC 2 die Viskositäten der verschiedenen Proben berechnet und mit den experimentell gefundenen Daten verglichen. Die universellen Werte ergaben Viskositäten, die große Unterschiede zu den gemessenen aufwiesen, während man bei Verwendung der optimierten Werte eine weitaus bessere Übereinstimmung erhielt.
    Notes: Summary The glass transition temperatures (T g ) of asphalt samples of different origins and penetration grades were determined by differential scanning calorimetry (DSC-2). TheT g values of samples originating from two sources decreased with increasing penetration whereas those of samples from a third source were identical at all values of penetration. Substituting theseT g data and values of the universal as well as the optimized constantsC 1 andC 2 in the Williams-Landel-Ferry equation, viscosities were calculated for each of the samples and compared with the corresponding experimental results. The universal values forC 1 andC 2 yielded viscosities which were far removed from the experimental data while the optimized values produced much better results.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1225-1239 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Copolymerization of elemental sulfur with styrene in the presence and absence of metallic sodium was studied at 120°C and 138°C. Propagation of the reaction was followed by gel permeation chromatography (GPC). Glass transition temperatures of all samples were obtained by differential scanning calorimetry (DSC). Reaction products were fractionated with a preparative-type GPC, and each fraction was characterized by DSC, vapor pressure osmometry, infrared spectrophotometry, and both proton and carbon-13 nuclear magnetic resonance spectrometry. Results indicate that the product is a true copolymer of styrene and sulfur. Kinetics of the copolymerization were studied using GPC to monitor styrene and sulfur concentrations. The initial rate of copolymerization (as followed by the consumption of styrene and sulfur) decreases with increasing initial styrene to sulfur ratio. From kinetic analyses, ratios of the rate constants of homo- and copolymerization were determined. Copolymerization of the reactants is more spontaneous than homopolymerization. The reactivity ratios obtained are 0.2 for styrene and 0.6 for sulfur.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2853-2866 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of 1,2-butylene oxide initiated with triphenylmethyl hexafluoroarsinate in the -20 to +25°C temperature range with 1,2-dichloroethane as solvent is characterized by a rapid nonstationary initial stage. This is followed by a second slower stage, during which the disappearance of monomer is first-order with respect to its concentration. The conversion of monomer at the end of the first stage is related to the initial catalyst concentration but not to the initial monomer concentration. Invoking the hypothesis of an instantaneous initiation reaction, the experimental results lead to the conclusion of the existence of a unimolecular termination step. Propagation-to-termination rate constant ratios yield a propagation-termination activation energy difference of 5.9 kcal/mole. The termination step proposed is thought to involve the formation of stable macrocyclic oxonium ions. These, in turn, can reactivate the polymerization by an intramolecular reaction leading to the formation of new active centers. An energy of activation of 8.7 kcal/mole was calculated for this reactivation. GPC analyses of the reaction products recovered at the end of the first stage revealed the presence of large proportions of oligomers. Based on kinetic data, the formation of oligomers is explained by a backbiting process similar to the reactivation reaction suggested for the initiation of the second stage.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 561-582 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The triphenylmethyl hexafluoroarsenate-initiated cationic polymerization of 1,2-butylene oxide in dichloroethane between -25 and +25°C and its sodium-initiated anionic polymerization in bulk at 20°C have been carried out. Gel permeation chromatography (GPC) molecular weight distribution curves of the reaction products are multinodal. Nuclear magnetic resonance (NMR) and infrared (IR) analyses show that the cationically prepared polymers are composed of cyclic oligomers and linear high-molecular-weight products, while the anionically prepared polymers contain only linear products some of which include double bonds. NMR analyses further reveal that the cationically prepared polymers consist of monomer repeat units, while the anionically prepared polymers are essentially made of side products originating from the reaction of 1,2-butylene oxide with the sodium mirror used as the anionic initiator.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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