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  • Wiley-Blackwell  (11)
  • 1970-1974  (11)
  • 1
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 3123-3131 
    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 thermal stabilities of polybutadienyllithium, polyisoprenyllithium, and polystyryllithium solutions have been determined in hydrocarbon solvents. Kinetic analysis indicated that a complex mechanism was involved in the thermolysis of polybutadienyllithium. The thermal stability was observed to increase with increasing lithium concentration, suggesting the presence of competitive reactions in addition to the expected elimination of lithium hydride. The thermal stability of the three systems studied was consistent with their reported degrees of association: dimeric polystyryllithium was less stable than tetrameric polyisoprenyllithium or hexameric polybutadienyllithium.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 3133-3144 
    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: In addition to the expected elimination of lithium hydride, metalation and addition reactions have been observed as competitive, thermolytic reactions of polybutadienyllithium. The importance of these reactions at temperatures frequently utilized for the polymerization of butadiene was illustrated and the effect of these reactions on the macrostructure of polybutadiene determined.
    Additional Material: 6 Ill.
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Linear oligourethanes with phenylurethane endgroups and cyclic oligourethanes were prepared from diethylene glycol and hexamethylene diisocyanate. The largest ring synthesized contains seven units of each, i.e., 119 ring atoms, with a molecular weight of 1920.An effective separation of the oligomers was achieved by adsorption column chromatography. An eluting solvent with solvent gradient was applied successfully. Melting points, transitions, long periods, and X-ray diffraction of the oligomers prepared are discussed with regard to their structure.
    Notes: Es wurden lineare Oligourethane mit Phenylendgruppen und cyclische Oligourethane aus Diäthylenglykol und Hexamethylendiisocyanat dargestellt. Der größte bisher isolierte Ring enthält je sieben Grundbausteine und besitzt 119 Ringglieder bei einem Molekulargewicht von 1920.Eine gute Trennung der Oligomeren wurde durch Adsorptionssäulenchromatographie erzielt. Hierbei wurde ein Elutionsmittel mit Lösungsmittelgradient verwendet. Schmelzpunkte, Umwandlungserscheinungen, Langperioden und Weitwinkeldiagramme der Oligomeren werden im Hinblick auf ihre Struktur diskutiert.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 164 (1973), S. 1-5 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 165 (1973), S. 51-57 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Mechanismus strahleninduzierter Polymerisationen im festen Zustand gab bisher vielerlei Anlaß zu Spekulationen. Da energiereiche Strahlen normalerweise im festen Monomeren sowohl Radikale als auch Ionen erzeugen, ist es schwierig zu unterscheiden, welche Art dieser Spezies tatsächlich die Polymerisation auslöst.Wir haben eine Methode entwickelt, die es erlaubt, kationische und anionische aktive Zentren zu unterscheiden. Kationische Polymerisationen werden durch Zugabe einer Base wie Natriumalkoholat in einem geeigneten Lösungsmittel abgebrochen; die Alkoxygruppe wird dabei in das Polymere als Endgruppe eingebaut. Diese Endgruppe wird nach Isolierung und Reinigung des Polymeren analytisch bestimmt. Der Einbau von Alkoxy-Endgruppen in das Polymere beweist das Auftreten von Polymerketten mit kationischen Kettenenden. Mit dieser Methode wurde gezeigt, daß bei der γ-strahleninduzierten Polymerisation von kristallinem Trioxan bei 60°C Polyoxymethylen-Kationen vorliegen. Es wird angenommen, daß das Kettenwachstum wie bei mit LEWIS-Säuren initiierten Polymerisationen über diese kationischen Zentren erfolgt.Anionische Kettenenden können auf analoge Weise bestimmt werden. Die Polymerisa-tionen werden durch Zugabe eines Überschusses an Alkyljodid abgebrochen, das mit anionischen Kettenenden unter Bildung von Alkoxy-Endgruppen reagiert. Überraschend wurden bei der strahleninduzierten Polymerisation von kristallinem Trioxan auch anionische Kettenenden im Polymeren gefunden. Es wird angenommen, daß diese Anionen nur als Gegenionen zu den wachsenden kationischen Kettenenden fungieren und selbst nicht zu einem Kettenwachstum führen
    Notes: The mechanism of radiation-induced polymerizations in the solid state has been a subject mostly open to speculation. As radiation usually generates several kinds of active species (radicals and ions) it is difficult to find out, which of these actually causes polymerization.We have developped a method distinguishing between cationic and anionic active centers. Cationic polymerizations are terminated by addition of a base such as sodium alkoxide in a suitable solvent. The alkoxide is incorporated into the polymer as an endgroup. This endgroup is determined analytically after isolation and purification of the polymer. The incorporation of alkoxy endgroups into the polymer is a proof of the occurrence of polymer chains with cationic chain ends. It was shown by this method that crystalline trioxane, polymerized by γ-rays at 60°C, contains polyoxymethylene cations. It is assumed that with these cationic active centers propagation is similar to polymerizations initiated by LEWIS acids. Anionic chain ends can be detected by an analogous way. Polymerizations are terminated by addition of excess alkyl iodide which produces alkoxy endgroups from the anionic chain ends. Surprisingly, in the radiation-induced polymerization of crystalline trioxane some anionic chain ends were also found in the polymer. It is assumed that these anions do not propagate and that they are only counter-ions of the propagating cationic chain ends.
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 135 (1970), S. 131-135 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Di-2-cyanoisopropylperoxide is formed when azobisisobutyronitrile is decomposed under oxygen in isobutyronitrile as a solvent. The yield amounts to ca. 5%. Thermal decomposition of the peroxide occurs with measurable rate only above 120°C by a first order reaction. The energy of activation in cumene as a solvent was found to be 37.9 kcal · mole-1. The rate constant of the decomposition reaction at 140°C amounts to 0.057 h-1 in cumene, to 0.073 h-1 in tert-butylbenzene, to 0.18 h-1 in chlorobenzene, and to 0.23 h-1 in o-dichlorobenzene.
    Notes: Das Di-2-cyanoisopropylperoxid entsteht in etwa 5-proz. Ausbeute bei der Zersetzung von Azoisobuttersäredinitril unter Sauerstoff in Isobutyronitril als Lösungsmittel. Thermisch zerfällt das Peroxid est oberhalb von 120°C mit meßbarer Geschwindigkeit in einer Reaktion erster Ordnung. Die Aktivierungsenergie, in Cumol als Lösungsmittel, wurde zu 37,9 kcal · mol-1 bestimmt. Werte für die Zerfallskonstante bei 140°C sind in Cumol 0,057 h-1, in tert-Butylbenzol 0,073 h-1, in Chlorbenzol 0,18 h-1 und in o-Dichlorbenzol 0,23 h-1.
    Additional Material: 1 Tab.
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ti4⊕ is reduced to Ti3⊕ in a chemical reaction that occurs between the components in the catalyst system Ti(OC3H7)4/Al(C2H5)2Cl. Polymerization is the last of a reaction sequence: (1) Reduction, gas evolution, colour changes; (2) formation of a solid phase; (3) polymerization. Not all of these reactions are studied in detail, but temperature, time and molar Al/Ti-ratio dependences are observed. Overall activation energy of catalyst formation is evaluated to about 17 kcal/mole.
    Notes: Zwischen den Katalysatorkomponenten Ti(OC3H7)4 und Al(C2H5)2Cl spielt sich eine chemische Reaktion ab; Ti4⊕ wird dabei zu Ti3⊕ reduziert. Die Polymerisation beginnt als letzte der aufeinanderfolgenden Reaktionen: (1) Reduktion von Ti4⊕, Gasentwicklung, Farbänderung; (2) Bildung einer festen Phase; (3) Polymerisation. Naturgemäß sind diese Reaktionen, die im einzelnen nicht alle untersucht wurden, abhängig von Temperatur, Zeit und molarem Al/Ti-Verhältnis. Die Brutto-Aktivierungsenergie der Katalysatorbildung ergibt sich zu ca. 17 kcal/Mol.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 156 (1972), S. 3-5 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 10
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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