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  • Chemistry  (20,531)
  • AERODYNAMICS
  • 1960-1964  (20,825)
Collection
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 15 (1962), S. 216-222 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Im Zusammenhang mit der früher bearbeiteten konduktometrischen Titration oberflächenaktiver Substanzen mit p-Toluidinhydrochlorid wurde die physikalisch-chemische Analyse des Systems Alkylsulfat/p-Toluidinhydrochlorid durch Bestimmung der Leitfähigkeit, Viskosität und deren Abweichungen von der Addierbarkeit durchgeführt. Auf Grund dieser Ergebnisse wurden die untersuchten Systeme als „irrationelle“ angenommen, was bedeutet, daß die charakteristischen Punkte, also die Extrema auf den Kurven der physikalisch-chemischen Eigenschaften  -  Zusammensetzung des Systems, einer stöchiometrischen Zusammensetzung der in der Lösung sich bildenden Verbindungen nicht entsprechen.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 10 (1964), S. 339-344 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 4 (1964), S. 22-24 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Bicyclo [2.2.1] hepta-2,5-diene, the reaction product of acetylene and cyclopentadiene, and vinyl chloride readily copolymerized by a novel mechanism, to form copolymers containing the nortricyclene group whose softening points rapidly increase with increasing nortricycl one concentration. For each weight per cent copolymerized bicycloheptadiene, the softening point of the vinyl resin is increased about 1°C, making it the most effective comonomer known for this purpose. At the same time increasing nortricyclene concentration disrupts polymer crystallinity, lowers the resin's melting point, and hence its processing temperature, by about 3°C for each weight per cent copolymerized.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 445-452 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monomer reactivity ratios have been determined for the copolymerization of methyl methacrylate (M1) and acrylonitrile (M2) catalyzed by alkyl derivatives of lithium, sodium, beryllium, magnesium, boron, aluminum, zinc, and cadmium. Lithium, sodium, beryllium, and magnesium alkyls gave reactivity ratios averaging r1 = 0.34, r2 = 6.7, while alkyls of boron, aluminum, zinc, and cadmium gave r1 = 1.24, r2 = 0.11. These values compare favorably with published reactivity ratios for anionic copolymerization (r1 = 0.25, r2 = 7.9) and free-radical copolymerization (r1 = 1.35, r2 = 0.18). Therefore, alkyl derivatives of groups Ia and IIa metals propagate by an anionic mechanism, while those of groups IIb and IIIa do so by a free-radical mechanism. Confirmatory experiments were run using styrene (M1)-acrylonitrile (M2) solutions. For groups Ia and IIa alkyls the reactivity ratios averaged, r1 = 0.20, r2 = 12.5; and for Groups IIb and IIIa r1 = 0.33, r2 = 0.03. The published values for free-radical catalysts are r1 = 0.41, r2 = 0.04. The formation of free radicals from the groups IIb and IIIa metal alkyls probably arises from oxidation of the metal alkyls by chance traces of oxygen.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 60 (1962), S. S36 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. S171 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 709-713 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2289-2297 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When vinyl chloride - methyl methacrylate copolymers having a uniform chain-to-chain composition, are pyrolyzed at temperatures around 150°C., an intramolecular lactonization occurs forming α-methyl-γ-butyrolactone groups in the polymer backbone concomitant with the quantitative elimination of methyl chloride. This reaction has been shown to be a general reaction for copolymers containing α-substituted γ-haloester groups in their backbone. The formation of the lactone groups in these polymers leads to increased chain rigidity and higher polymer softening points. Advantage has been taken of the gaseous alkyl halide elimination to produce rigid vinyl foams of good compressive strengths.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2231-2236 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Bicyclo[2.2.1]hepta-2,5-diene, in the presence of free-radical initiators, homopolymerizes to a low molecular weight, soluble polymer containing both 3,5-disubstituted nortricyclene and 5,6-disubstituted bicyclo [2.2.1] hept-2-ene units in the polymer backbone. When the bicycloheptadiene (M2) is copolymerized with vinyl chloride, vinylidene chloride, acrylonitrile, ethyl acrylate, and methyl methacrylate, only the transannular product, 3,5-disubstituted nortricyclene, is found in the high molecular weight copolymers. Reactivity ratios for the above mentioned copolymerizations at 50°C. are: r1 = 0.74, r2 = 0.35; r1 = 1.41, r2 = 0.08; r1 = 0.67, r2 = 0.08; r1 = 3.05, r2 = 0.01; r1 =10.0, r2 = 0; respectively. From these data, the Q and e values for bicyclo[2.2.l]hepta-2,5-diene average 0.09 and -1.04, respectively.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1274-1279 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Erschöpfende Ozonisierung von (-)-Epicatechin und Reduktion der optisch aktiven Ozonisierungsprodukte führte zu 2-Desoxy-D-xylit, welcher als Tetraphenylurethan in reiner Form isoliert, charakterisiert und identifiziert wurde. Der von D-Glycerinaldehyd sterisch eindeutig abgeleitete 2-Desoxy-D-xylit enthält die beiden asymmetrischen C-Atome 2 und 3 des (-)-Epicatechins in unveränderter Konfiguration. Für (-)-Epicatechin folgt daraus zwingend die absolute Konfiguration gemäss Formel I, wie sie erstmals von K. FREUDENBERG u. a. durch vergleichende Betrachtung von Drehungsverschiebungen aus der Ephedrin- und Mandelsäure-Reihe abgeleitet wurde.
    Additional Material: 2 Tab.
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