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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 71 (1949), S. 1542-1550 
    ISSN: 1520-5126
    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
    Journal of the American Chemical Society 75 (1953), S. 2522-2523 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 47 (1955), S. 1281-1286 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 171 (1953), S. 842-843 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Absorption spectra of the ethyl chlorophyllides in ether. Solid lines, abs9rption spectra of chlorophylls a and b, from Harris and Zscheile (ref. 2); open circles and filled circles, relative absorption coefficients for ethyl chlorophyllides a and b respectively This has now been tested directly. ...
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 162 (1948), S. 452-453 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IN a paper concerned chiefly with the results of measurements of the self-quenching of the fluorescence of solutions of aromatic hydrocarbons1, Weiss and Weil-Malherbe report a few measurements on the self-quenching of ethyl chlorophyllide solutions. They conclude from these ...
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 101-106 
    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: The degradation on mastication of polymers brought into a rubbery state by incorporation of liquids or rise in temperature is accounted for by the mechanicochemical mechanism previously advanced to explain the degradation of rubbers. The dependence of the reaction on shear rate has been shown indirectly, as with rubbers, by the negative temperature coefficient of reaction, and also directly by variation of masticator rotor speed and design. A further new feature is the influence of the nature as well as concentration of plasticizer on the rate of degradation and a correlation with the softening of the polymer. A limiting molecular weight is reached on prolonged mastication from whatever initial molecular weight.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 245-249 
    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: A comparison between the viscosity-molecular weight relationships for natural rubber degraded in thin films at 130 and 140°C. and on cold and hot mastication indicates a greater similarity of distribution on degradation by the mastication treatments. The hot mastication process is further differentiated from ordinary thermal reactions by the dependence of rate of degradation on the rate of shear. It does, however, differ from cold mastication in being primarily an oxidative-scission reaction. No differences were detected in the properties of networks prepared from rubbers masticated at high or low temperatures to the same level of degradation.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 367-368 
    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
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 2 (1947), S. 229-245 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A review of theoretical progress in copolymerization has shown that the results of previous authors are consistent and equivalent. A general scheme of copolymerization has been stated and its kinetic consequences worked out. The rate expressions have been derived for percentage polymerization against time, and initial rate against initial monomer concentration. Some experimental considerations have been given. The advantages of photochemical technique have been stressed, physical means of following the reaction outlined, and new methods of determining σ and μ described. Means of verifying the kinetics have been suggested, in particular the obtaining of the individual velocity constants. It is important to note in this connection, that further experiments to determine the lifetime of the growing polymer chain are not required.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 19 (1956), S. 237-254 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Natural rubber vulcanizates have been prepared by a method permitting determinations by chemical analysis of the number of crosslinking introduced. The crosslinking agent was di-tert-butyl peroxide, and the peroxide and its decomposition products-tert-butanol, acetone, methane, and ethane - were determined by infrared spectroscopic and manometric methods. tert-Butanol and methane result from the abstraction of α-methylenic hydrogen atoms from the rubber hydrocarbon by means of tert-butoxy and methyl radicals, respectively. On the assumption that the resultant rubber hydrocarbon radicals undergo exclusive mutual combination a chemical evaluation of degree of crosslinking, 1/2 Mc, is given by ½(moles of tert-butanol + moles of methane), where Mc is the average molecular weight between crosslinks. Physical values of 1/2 Mc for rubber of infinite initial molecular weight have been obtained by determining the volume fraction of swollen rubber, vr-, in n-decane, and by using the method described in Part I for correcting for the finite initial molecular weight of the rubber. A comparison of the physical and chemical values of 1/2 Mc indicates that the former is greater than the latter for all degrees of crosslinking, the major divergence being accounted for by an additive term which is pictorially visualized as due to entanglements.
    Additional Material: 7 Ill.
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