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  • Superfluidity and superconductivity  (14)
  • Chemistry  (9)
  • Computer Systems
  • Nonlinear Dynamics and Chaos
  • 2015-2019  (18)
  • 1970-1974  (4)
  • 1960-1964  (5)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2199-2209 
    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 kinetics of low-temperature (60-100°C.) thermal degradation of deproteinized and deresinified petroleum ether soluble fraction of natural rubber in two chemically inert solvents, cyclohexane and trans-decalin, have been studied. The changes in Mw, A2, and (r2)1/2 at various stages of degradation have been obtained from the lightscattering data. The rate constants and the energy of activation for chain scission have been calculated from the observed variation in Mu. The scission has been found to be random and the average energy of activation is 25.8 kcal./mole. This low-energy requirement suggests the presence of weak links in the rubber molecule which get ruptured at low temperature.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 21 (1963), S. 147-148 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The coulometric determination of tripositive arsenic and antimony by electrogenerated iodine in a NaHCO3 buffered solution of pH 8 has been described. The end point can be determined visually using starch as an indicator. Quantities of As(III) and Sb(III) down to the microgram level can be determined within permissible limits of error.
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 163 (1973), S. 37-43 
    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: Die Substanzpolymerisation von N-Vinylcarbazol (NVC) wurde mit 3d-Metalloxid-Katalysatoren durchgeführt, und die folgende Reaktivitätsreihe für die untersuchten Oxide wurde vorgeschlagen: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm 2} {\rm O}_{\rm 5} {\rm 〉 MnO}_{\rm 2} {\rm 〉 TiO}_{\rm 2} {\rm 〉 Cr}_{\rm 2} {\rm O}_{\rm 3} {\rm 〉 NiO 〉 ZnO 〉 Cu}_{\rm 2} {\rm O 〉 CuO 〉 Co}_{\rm 3} {\rm O}_{\rm 4} {\rm andCoO} $$\end{document} wobei die Oxide des Kupfers und Kobalts nicht wirksam sind. Einige kinetische Untersuchungen wurden mit dem System NVC/MnO2 ausgeführt. Auf Grund der Verzögerung der Polymerisationsgeschwindigkeit bei Gegenwart von Wasser oder Thiophen wurde ein kationischer Mechanismus für die Polymerisation vorgeschlagen. Die Wirkungslosigkeit der Kupfer- und Kobaltoxide als Katalysatoren wurde vorläufig mit der Annahme gedeutet, daß sie eher oxydierend wirken als durch π-Komplex-Bindung. Rühren übt keinen Einfluß auf die Polymerisationsgeschwindigkeit aus.
    Notes: The bulk polymerization of N-Vinylcarbazole (NVC) is carried out using some 3 d-metal oxides as catalysts and the following order of reactivity is suggested for the various metal oxides studied: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm 2} {\rm O}_{\rm 5} {\rm 〉 MnO}_{\rm 2} {\rm 〉 TiO}_{\rm 2} {\rm 〉 Cr}_{\rm 2} {\rm O}_{\rm 3} {\rm 〉 NiO 〉 ZnO 〉 Cu}_{\rm 2} {\rm O 〉 CuO 〉 Co}_{\rm 3} {\rm O}_{\rm 4} {\rm andCoO} $$\end{document} the oxides of copper and cobalt being ineffective. Some kinetic studies are carried out with the NVC/MnO2 system. Endorsed by the observed retardation of the rate in the presence of water and thiophene a cationic mechanism is suggested for the polymerization. The incapability of the oxides of Cu and Co to act as good catalysts is tentatively explained by supposing that they act as oxidizing rather than π-complexing polymerization catalysts. Stirring does not show any influence on the rate of polymerization.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 151 (1972), S. 121-125 
    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: Die Störung der Metachromasie eines an einem Polyanion gebundenen Farbstoffs durch Cetylpyridiniumchlorid (CPCl) wurde quantitative abgeschätzt, indem die in der wässerigen Schicht verbliebenen Farbstoffmengen nach Schütteln der metachromatischen Lösung mit Tetrachlorkohlenstoff in An- und Abwesenheit von CPCl ermittelt wurden. Die Aufhebung der Metachromasie wurde außerdem aus der konduktometrischen Titration der Farbstoff/Polyanion-Lösung mit CPCl ermittelt. CPCl verdrängt die Farbstoffionen von den Polyanionen beinahe stöchiometrisch, was bei Natriumchlorid nicht der Fall ist. Dieses besondere Verhalten von CPCl wird seiner Neigung zur Bildung hydrophober Bindungen zugeschrieben. Es wurden Methylenblau und Kristallviolett als Farbstoffe sowie Chondroitinschwefelsäure und Heparin als Polyanionen verwendet
    Notes: The disturbance of metachromasia of a dye/polyanion system by cetyl pyridinium chloride (CPCl) has been estimated quantitatively from the difference of the amounts of dye left in the aqueous layer after carbon tetrachloride extraction of the metachromatic solution in the presence and absence of CPCl, as well as from conductometric titration of the dye/polyanion solution with CPCl. Results show that CPCl, unlike sodium chloride, displaces the dye ions from the polyanions almost stoichiometrically. This special behaviour of CPCl has been assigned to its tendency to form hydrophobic bonds. As dyes methylene blue and crystal violet, as polyanions chondroitin sulfate and heparin have been used.
    Additional Material: 2 Ill.
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  • 5
    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 convenient method of preparing zinc ethylenediamine complex (ZED) solution for use as solvent for cellulose pulp is described, and the advantages in using this solvent (0.25M zinc in 41% ethylenediamine in water) over cupriethylenediamine (CED) or cuprammonium solutions for viscometric determination of molecular weight of cellulose are indicated. Intrinsic viscosities of eight rayon-grade pulp solutions have been determined at four temperatures: 15, 20, 25, and 30°C. The constants K = 5.85 × 10-5 and a = 0.936 of the Mark-Houwink equation [η] = KMna, required for evaluating the molecular weight of cellulose pulps in ZED solution, have been determined by using the molecular weight values obtained from CED solutions.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 2653-2659 
    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: Sol rubber dissolved in three solvents - cyclohexane, petroleum ether (40-60°C. fraction), and toluene - was degraded by ultrasonic waves, the degradation kinetics being followed by measuring spectrophotometrically the consumption of the free radical scavenger α,α′-diphenyl-β-picryl hydrazyl. The kinetic data have been examined by the rate equations developed from two different approaches: one by Jellinek and the other by Ovenall. It has been observed that the number of bonds broken as a function of time can be fitted equally well by both equations in the initial stage, but as the time of degradation increases, especially when the number-average degree of polymerization attains a value less than 3Pe/2, the rate can be described better by Jellinek's equation than that of Ovenall. The rate constants K and the final degree of polymerization for rubber are found to depend on the nature of the solvent.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 11 (1973), S. 639-643 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 12 (1974), S. 543-543 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 1471-1479 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of organic solvents on the rate of heterogeneous aqueous polymerization initiated by the K2S2O8—Na2S2O4 redox pair has been studied. The separating polymer phase remains in colloidal dispersion, the stability of which is partly due to charge and partly due to hydration. Both the water-miscible and water-immiscible organic liquids decrease the rate of polymerization, the limiting conversion, and the molecular weight of the polymers. It has been suggested that the water-miscible organic liquids preferentially solvate the latex particles and thereby decrease the hydration stability and monomer concentration in the latex particles, whereas the water-immiscible organic liquids decrease the monomer concentration in the latex particles due to the partition of the monomer between the aqueous and the nonaqueous phases. Thus the fall in the rate and molecular weight of the polymers may be ascribed to the increase in the termination rate by the faster coagulation of the latex particles and dilution of monomer concentration at the reaction site.
    Additional Material: 3 Ill.
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  • 10
    Publication Date: 2016-06-14
    Description: Author(s): P. K. Biswas, D. G. Mazzone, R. Sibille, E. Pomjakushina, K. Conder, H. Luetkens, C. Baines, J. L. Gavilano, M. Kenzelmann, A. Amato, and E. Morenzoni The recent discovery of the topologically protected surface states in the β phase of PdBi 2 has reignited the research interest in this class of superconductors. Here, we show results of our muon spin relaxation and rotation ( μ SR ) measurements carried out to investigate the superconducting and magnet… [Phys. Rev. B 93, 220504(R)] Published Mon Jun 13, 2016
    Keywords: Superfluidity and superconductivity
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
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