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  • Polymer and Materials Science  (119)
  • ELECTRONICS  (47)
  • 1965-1969  (166)
  • 1950-1954
  • 1940-1944
  • 1968  (166)
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Publisher
Years
  • 1965-1969  (166)
  • 1950-1954
  • 1940-1944
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 2191-2200 
    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: Infrared and NMR group-type methods for the analysis of the anhydride content of maleic anhydride copolymers such as poly(maleic anhydride-co-α-olefin) and the half ester content of their reaction products with alcohols are described. The infrared analyses are based on the integrated absorptivities of the anhydride carbonyl and the combination of the acid and ester carbonyl. The NMR method is based on the intensities of the various chemically shifted groups in the copolymer. The use of dimethyl sulfoxide as an auxiliary solvent has made the infrared analysis possible.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 871-883 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The following measurements were carried out on the melts of two samples of polypropylene, one with a narrow and one with a broad molecular weight distribution: viscosity in steady shear flow, dynamic storage and loss moduli, total normal thrust in cone-and-plate apparatus, and flow birefringence. The validity of various theoretical interrelations between the measured quantities is checked. The influence of molecular weight distribution is qualitatively discussed.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 165-180 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spherulitic growth data that exist in the literature for a wide diversity of polymers have been analyzed according to various possible nucleation mechanisms. It is demonstrated that, if allowed a reasonable choice for the equilibrium melting temperature, no unbiased selection of a unique nucleation process can be made. Moreover, a set of universal parameters exists for each of the allowable nucleation processes which enables the data to be represented by a single straight line which encompasses all the polymers. The only quantities specific to a given polymer are the equilibrium melting temperature and the activation energy for transport. The magnitude of the latter quantity is shown to be dependent on the glass temperature of the polymer.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 1343-1353 
    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 discrete relaxation spectrum of an ABS (acrylonitrile-butadiene-styrene) polymer at 190°C. was calculated by using results from tensile relaxation moduli and the principle of reduced variables. The shift factor was found to conform well to the WLF equation, and the free volume fraction at Tg was calculated to be 0.026 in good agreement with the universal value. The values of the thermal expansion coefficient of free volume were calculated to be 9.8 X 10-4 deg.-1 and 7.0 × 10-4 deg.-1, respectively, from the WLF coefficients and from dilatometric results. The width of the entanglement plateau of the relaxation spectrum was observed to be a factor of approximately 2 larger than that calculated from molecular weights between entanglement couplings determined either from rubber elasticity theory or from an assumed molecular model which discounts the presence of the butadiene in the ABS system. By using Pao's theory, flow curves at 190°C. were calculated both from the discrete relaxation spectrum and from the dynamic modulus. These curves were essentially identical. However, the stress values of these curves were found to be about a decade higher than those experimentally determined from capillary flow measurements. Nevertheless, the shapes of the curves are in good agreement, and an explanation is suggested for existing discrepancies. Flow instability, processing variables, and residual strains are discussed in light of the flow curves and the calculated recoverable shear strains.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 527-532 
    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: Unsteady-state water sorption measurements have been carried out over the temperature range 27-40°C. on a polyurethane elastomer composed of MDI, 1,4-butanediol, and polybutylene adipate (MW 2000) in the mole ratios 3.2:2:1. The sorption isotherm is concave upward above an activity of 0.6, reaching a saturation water concentration of 1.6 g./100 cc., the heat of mixing is zero, and the diffusion constant decreases slowly and linearly with increasing water concentration. The overall behavior is attributed to the immobilization of sorbed water in clusters. Analysis of the sorption process in terms of the cluster integral reveals that the interaction of water with specific polymer sites occurs at the lowest concentrations but that clustering dominates for water activities greater than 0.45. Since the activation energy for diffusion decreases with increasing water concentration, from 11,000 cal./mole at zero concentration to about half that value at saturation, plasticization of the polymer also affects the transport process.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 2 (1968), S. 407-427 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The in vitro behavior of a number of Au-Fe precipitation-hardenable alloys have been investigated in distilled water and in Ringer's solution (simulating the extracellular body fluids) by the open-circuit potential versus time method. The in vivo behavior of these materials as muscle implants has been studied by conventional histopathological and histochemical techniques. Optical and electron microscopic techniques have been used to study the extent and morphology of massive discontinuous precipitation as well as the mode of corrosion attack. A clear correlation has been established between the microstructural features presented by a given alloy and the time-dependent open-circuit potential and in vivo corrosion behavior. It can be concluded for this alloy system that the microstructure and the open-circuit potential pattern may be taken to be a reasonable indication of the expected in vivo corrosion behavior.
    Additional Material: 16 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 117 (1968), S. 231-241 
    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: It is shown that the phase of a mixture of high pressure polyethylene and isotactic polypropylene depends on temperature, weight fraction, and molecular weight of the polymers. Mixtures with high polypropylene content form solid solutions. A variation of the molecular weight of polypropylene has a significant effect on the phase state of the mixture, the molecular weight of polyethylene does not. The phase diagram can be represented best in a three-dimensional coordinate system with temperature, composition, and molecular weight of polypropylene as coordinates.
    Notes: Der Phasenzustand des aus Hochdruckpolyäthylen und isotaktischem Polypropylen bestchenden Polymerengemisches wurde in Abhängigkeit von der prozentualen Zusammensetzung und von den Molekulargewichten der Komponenten untersucht. Es zeigte sich, daß der Phasenzustand von der Temperatur, dem Gewichtsverhältnis der Komponenten und dem Molekulargewicht der Polymeren abhängt. Feste Lösugen bilden sich bei einem hohen Polypropylengehalt des Gemisches. Das Molekulargewicht des Polyäthylens wirkt sich nicht merklich aus, dasjenige des Polypropylens hingegen beeinflußt den Phasenzustand des Gemisches. Das Zustandsdiagramm des Polymerengemisches wird am besten in einem räumlichen Koordinatensystem mit Temperatur, Zusammensetzung und Molekulargewicht des Polypropylens als Koordinaten dargestellt.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 117 (1968), S. 224-230 
    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 Polymerisation von Styrol mit dem Katalysatorsystem VOCl3/Li(iC5H11) wurde untersucht. Die Polymerisationsgeschwindigkeit fällt mit zunehmendem Li/V-Verhältnis stark ab; die Molekulargewichte der erhaltenen Polymeren haben dagegen bei Li/V = 1 ein Maximum. Die Reaktion ist in bezung auf den Katalysator und das Monomere von der 1. Ordnung. Die Aktivierungsenergie beträgt 5,67 kcal/mol. Zinkdiäthyl wirkt als Überträger. trans-Stilben hat keinen Einfluß, weder auf die Molekulargewichte noch auf die Reaktionsgeschwindgkeit. Bei einem molaren Li/V-Verhältnis von 1 beträgt die mittlere Wertigkeit des Vanadiums 4,12; mit zunehmendem Li/V-Verhältnis fällt sie ab.
    Notes: The polymerization of styrene with the VOCl3/Li(iC5H11) catalyst system has been studied. Rates of polymerization fall sharply with increase in Li/V ratio; the molecular weights, however, show a maximum at Li/V = 1. Polymerization is first order with respect to catlyst as well as monomer concentrations. Activation energy was found to be 5.67 kcal/mole. Zinc diethyl acts as chain transfer agent. There was no effect of trans-stilbene on molecular weights as well as on rate of polymerization. Valence of vanadium at Li/V molar ratio 1 is 4.12 and it decreases with increase in ratio.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 6 (1968), S. 493-497 
    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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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 193-203 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of styrene with two catalyst systems consisting of Al(C2H5)3 in combination with ZrCl4 or ZrCl3 has been studied. The rate of polymerization with catalyst concentration was first-order with ZrCl4 system and second-order with ZrCl3 system, but at higher catalyst concentrations in both cases, the rate progressively decreases and finally attains a low value. The rate of polymerization is, however, proportional to the square of the monomer concentration in both the cases. The overall energy of activation was 10.9 kcal./mole and 6.45 kcal./mole in these systems. The polymers obtained with ZrCl4 were of lower molecular weights as compared to those obtained with ZrCl3. The polymers in both the cases had amorphous character.
    Additional Material: 13 Ill.
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