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  • Polymer and Materials Science  (21)
  • Inorganic Chemistry  (3)
  • Aerodynamics  (2)
  • GENERAL  (2)
  • Chemical Engineering
  • 1985-1989
  • 1970-1974
  • 1955-1959
  • 1950-1954  (28)
  • 1952  (28)
Collection
Keywords
Publisher
Years
  • 1985-1989
  • 1970-1974
  • 1955-1959
  • 1950-1954  (28)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 321-335 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vulcanization with sulfur is ascribed to the formation of sulfur radicals which are believed to copolymerize with the rubber molecule double bonds. Hydrogen sulfide is proposed as necessary for chain initiation but when formed in sufficient amounts serves as a chain terminator. This is believed to lead to numerous self-limiting features including ceiling temperatures, post-vulcanization and delayed action effects. Initiation may result from the oxidation of H2S to sulfur radicals and termination to the formation of HS radicals.
    Additional Material: 2 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 409-423 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When the acetate groups of polyvinyl acetate are removed and subsequently restored, the viscosity of the polymer is usually decreased. It is found that after such processing, vinyl acetate polymers prepared at a given temperature approach a maximum viscosity regardless of the viscosity of the original resins. This maximum is increased by lowering the temperature of polymerization and is different for other vinyl esters. The extent of degradation is negligible at low conversions. It is concluded that this phenomenon is characteristic of the monomer. The chemical bond responsible for the degradation has many of the properties of ester linkages. The resins degrade with both bases and acids although the latter catalyst sometimes requires the presence of water. They also degrade when heated in a solution of pyridine, acetic acid and acetic anhydride. The extent of degradation closely parallels the degree of hydrolysis. It is suggested that these ester linkages are formed during polymerization as a result of transfer with the carbon-hydrogen bonds of the acetate groups of both monomer and polymer. Evidence of another transfer reaction involving the vinyl group, but having no bearing on the degradation, is also advanced. If polyvinyl acetate is alcoholized with an acid catalyst, in the absence of water, the processed resin may have a higher viscosity than would be the case with an alkaline catalyst. How much higher is governed by the type of initiator used in the polymerization. This suggests that polymer molecules may be united under these conditions, but the nature of the reaction is obscure.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 269 (1952), S. 120-134 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kristallitgrößen der bei thermischer Zersetzung von Dolomit entstehenden Reaktionsprodukte wurden mit Hilfe eines Geiger-Zählrohr-Spektrometers aus der Verbreiterung von Röntgeninterferenzen bestimmt.Bei Zersetzung zu MgO und CaO nimmt die Größe der Kristallite von etwa 60 bzw. 130 Å an mit steigender Temperatur stetig zu. Oberhalb etwa 900° C erfolgt ein starker Anstieg der Kristallitgröße. Die Primärteilchen werden dann größer als etwa 1000 Å, womit die methodisch bedingte obere Grenze der bestimmbaren Kristallitgröße erreicht ist.Bei partieller Zersetzung zu MgO und CaCO3 tritt in der Abhängigkeit der Kristallitgrößen von der Reaktionstemperatur ein Minimum für beide Zersetzungsprodukte auf. Dies erklärt sich durch Überlagerung zweier Einflüsse, der Kristallkeimbildung und des Kristallwachstums. Diese Erscheinung ebenso wie der Befund, daß die CaCO3- bzw. CaO-Kristallite stets beträchtlich größer sind als die MgO-Teilchen, ist in übereinstimmung mit dem aufgefundenen Reaktionsmechanismus der Dolomitzersetzung.Auch bei sinkender Reaktionstemperatur (〈650° C) wird eine gewisse Kristallitgröße nicht unterschritten. Die Zersetzungsreaktionen laufen nämlich mit nennenswerter Geschwindigkeit erst bei Temperaturen ab, bei denen hinreichende Beweglichkeit der Gitterbestandteile vorhanden ist, so daß dann auch bereits Kristallite gebildet werden können.Durch Messung von Integralintensitäten wurde gefunden, daß die Reaktionsprodukte frei von solchen Gitterstörungen sind, welche die Integralintensität beeinflussen.
    Additional Material: 5 Ill.
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  • 4
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Diäthylacetale des d,l- und d(+)-Pantothenals wurden hergestellt und einer milden Verseifung und Oxydation unterworfen, wobei in gewissem Maße Salze der entsprechenden Pantothensäuren gebildet wurden. Aus dem d,l-Pantothenal - diäthylacetal entstand durch Säurebehandlung eine hochschmelzende Verbindung, für die die vorläufige Formel eines „Dipantothenals“ (II) vorgeschlagen wird. Im Ratten-Wachstumsversuch Zeigt diese Substanz eine deutliche Vitaminwirkung.
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  • 5
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch die Bestimmung der physikalischen Konstanten, sowie durch Ozon-Abbau zu den beiden Cyclopropan-dicarbonsäuren-(1.2), wurde die 2-Phenyl-cyclopropan-carbonsäure-(1) vom Schmp. 107° als die cis-Säure, die 2-Phenyl-cyclopropan-carbonsäure-(1) vom Schmp. 93° als die trans-Säure erkannt.
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  • 6
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Branching and cross-linking are noted in emulsion and mass polymerizations involving vinyl benzoate and nuclearly substituted vinyl benzoates. A theory is proposed to account for this phenomenon based on free radical addition to the benzoate nucleus. Six new vinyl esters of substituted benzoic acids are described.
    Additional Material: 3 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 365-370 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction of polymethacrylamide, [-CH2C(CH3)(CONH2)-]n, in aqueous solution with hypobromite and hypochlorite has been investigated. Different reaction procedures yielded polymers which were similar, and which contained a small number of primary amino groups, considerable carboxyl and unreacted amide groups and, probably, alkylacylurea groups formed by interaction between adjacent isocyanate and halogenoamide groups. Analytical data supporting these conclusions are presented. The polymer from the Hofmann reaction is soluble in dilute alkali and also in strongly acid media, precipitating on dilution. Methacrylamide monomer reacts with hypochlorite to give N-α-methylvinyl-N′-methacrylurea and acetone.
    Additional Material: 5 Ill.
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  • 8
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When heated in a vaccum at 325° to 375°C., polystyrene yields mainly the monomer and some dimer, trimer, tetramer, etc., indicating that the breaks in the molecular chains occur largely at the ends. Polyethylene, under similar conditions, but at a some-what higher temperature, yields fragments of an average molecular weight of about 700, indicating that the molecular chains break, mostly at random positions. A study was made of rates of thermal degradation of these two polymers by measuring rates of loss of weight of samples by means of a very sensitive tungsten spring balance enclosed in a vaccum. The samples were limited to 5-6 mg. in order to avoid spattering during degradation. Rate curves plotted against per cent loss of weight by volatilization indicate that in the case of polystyrene the process is intermediate between a zero and first order reaction, while in the case of polyethylene, the process approximates a first order reaction. Activation energies were calculated on the basis of rates of degradation at various temperatures. The values thus obtained for polystyrene and polyethylene are 58 and 68 kilocalories, respectively.
    Additional Material: 14 Ill.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: (1) Sebacamide and N,N′-diacetylhexamethylenediamine interchange to produce acetamide and polyhexamethylene sebacamide. (2) The rate is proportional to the concentrations of the two reacting species and to the square root of carboxyl group concentration. (3) The rate increases with increasing concentration of water. Reagents which had been held in the molten state under high vacuum were still capable of reaction. (4) N-Substitution decreases the rate constant; the isobutyl group is more effective than methyl in this respect. (5) As an indication of the amount of interchange occurring during a typical polymerization, it is computed that at least 42% of the amide links interchange during the 66 nylon synthesis. This means that it is not feasible to make nonrandom copolyamides by polymerizing together low molecular weight homopolyamides. Interchange does provide for the production of nonrandom copolymers from two or more high molecular weight homopolyamides.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 93-95 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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