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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 6 (1982), S. 501-508 
    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 It had been studied the applicability of coated silicagel as stationary phase in size exclusion chromatography of cellulose nitrate. Sample concentration and injection volume had been standarized. The elution volumes corresponding to discrete molecular weights resulted in a high reproducibility provided the application of the standarized conditions. There does not occur any adsorption of the cellulose nitrate on the packing material. It could be confirmed that separation takes place by a size exclusion mechanism. Separation power of the system had been proved by comparing the distribution curves obtained by means of GPC and fractionation precipitation respectively on the same sample.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 11 (1984), S. 281-286 
    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 There had been studied the calibration conditions on the system cellulose nitrate (sharp fractions) -THF-μ-Styragel by comparing the viscosity averages of DP obtained from the elution curves of GPC with the corresponding viscosimetrically determined ones. Deriving the elution volumes from the integral elution curves and applying adjustment of the calibration by means of adequate iterations, a very good coincidence between DPn(visc.) and DPn(GPC) can be reached. The molecular weight distribution curves obtained by GPC and by precipitation fractionation agree within the limits of error of both methods. It appears, however, that if in the calibration only one kind of average value of the “master” samples had been involved, only the same type of average can be determined with satisfying exactness.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 175 (1990), S. 117-128 
    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: Für das System Cellulosenitrat-μ-Styragel-THF wurde die DP-Ve-Beziehung sowie die Ausarbeitung der betreffenden Eichparameter einer genaueren Betrachtung unterzogen. Die etwa dreißig Eichpräparate waren durch definierten säurekatalysierten Abbau von Baumwollcellulose und anschließende Nitrierung hergestellt worden und umfaßten einen DP-Bereich von 150 〈 DP 〈 8000. Es wird gezeigt, daß mit steigendem DP die DP-Ve-Beziehung drei verschiedene Phasen aufweist. Bei der Anwendung der SEC auf Cellulosenitrat müssen daher bezüglich der Eichung zwei Fehlerquellen in Betracht gezogen werden: eine bezieht sich auf die Methode der Ausarbeitung der Eichparameter als solche, und die andere auf die Nichtbeachtung des Vorhandenseins dreier Abschnitte in der DP-Ve-Beziehung. Die Auswirkung dieser Fehler auf die Genauigkeit der aus den Elutionsdiagrammen abgeleiteten Verteilungskurven und DP-Mittelwerte wird diskutiert.
    Notes: The calibration behaviour of the system cellulose nitrate-μ-Styragel-THF has been studied using about 30 different calibration samples prepared by defined acid catalyzed degradation of cotton cellulose. The samples covered a range of DP between 150 〈 DP 〈 8000. It is shown that the DP-Ve relationship is characterized by the existence of three subsequent stages. Consequently, two sources of errors in the DP-Ve calibration must be taken into consideration. One refers to the methods as such to elaborate the calibration parameters, and the other one arises by neglecting that the DP-Ve relationship involves 3 distinct stages. The extent of the two classes of errors in regard to the exactness of the determined molecular weight averages and molecular weight distributions is discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 1984-01-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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  • 5
    Publication Date: 1982-01-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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