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  • Physics  (47)
  • 1980-1984
  • 1970-1974  (47)
  • 1973  (47)
  • 1
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular core binding energies have been measured by ESCA for the homopolymers of ethylene and the fluoroethylenes. The data are interpreted in terms of semiempirical all-valence electron SCF MO calculations in the CNDO/2 formalism, in conjunction with the charge potential model. The results are used as a basis for interpreting the measured core binding energies of some Viton and Kel F type polymers. The routine application of ESCA to the determination of copolymer compositions is described.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1867-1879 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electroinitiated copolymerization of styrene and diethyl fumarate in methanol solvent with zinc bromide as electrolyte has been investigated at high current strengths (200-500 mA). Unlike the copolymerization behavior observed at lower current strengths (〈 200 mA), it is found that the cathodically produced copolymers deviate from a 1:1 composition and show a significant deficiency in styrene. The copolymer products can be separated into two well-defined fractions: a toluene-soluble fraction (normal copolymer) and a toluene-insoluble one (styrene-deficient copolymer). These deviations in copolymer composition from a 1:1 monomer ratio are attributed to the occurrence of cathodically induced electroreductive hydrolysis side reactions with diethyl fumarate leading to the formation of carboxylate or acid salt species. Reaction of these hydrolyzed species with diethyl fumarate results in the formation of fumarate-rich copolymers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 391-392 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 457-465 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An approximate model is developed which relates the twisting seen in the spherulitic crystallization of many materials to surface stresses. Expressions are presented for the twist period as a function of the surface stress. These are compared with previous experimental data on polyethylene and data on hippuric acid obtained in the present investigation. In both cases the experimental data are in accord with the predictions of the model.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 89-104 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure of the tetrameric dianion formed by α-methylstyrene in tetrahydrofuran by reaction with sodium has been examined. Mass spectral, NMR, infrared, and kinetic data all indicate that the structure is rather than the structure which had previously been assumed for this species.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 175-189 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Separations of carboxyl-terminated polybutadiene (CTPB) liquid polymer according to functionality have been effected by using stepwise elution from silica gel. Recoveries in the 90-95% range have been achieved by deactivating the silica gel and recycling the unfractionated portion through progressively more active silica gel. Subjection of the fractions obtained from the silica-gel separation to analysis via gel-permeation chromatography and infrared spectroscopy yields not only functionality distribution data, but also provides an estimation of the relationship between molecular weight distribution and functional type. Repetitive analyses indicate a precision of ±7% (or less) of the amount of each functionality type present. An evaluation has been made of the accuracy of the data by fractionating saturated and methyl ester derivatives of CTPB under test conditions different from those employed in fractionating the original polymer. Within the known experimental error of the techniques employed, these studies have confirmed the data generated for CTPB polymer as received. Analytical techniques and interpretation of data are discussed.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 253-259 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polybutadiene of high molecular weight was prepared in hydrocarbon solvent by using n-BuNa-tert-BuOM (M = Li, K) as a polymerization initiator. The microstructure of this polymer varied from 35 to 76% of 1,2 content, depending on the type of modifiers. The kinetics of polymerization was not studied, primarily due to the heterogeneous nature of the catalyst. However, other variables, such as the catalyst concentration and temperature, have been studied. The results and mechanistic implications are discussed.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 905-907 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2601-2613 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spectroscopic studies made on the bisphenol A polycarbonate-sulfur dioxide system showed evidence of interaction between polymer and penetrant. Equilibrium studies made on solutions of sulfur dioxide and organic carbonates chosen as monomer analogs showed that complexes of the donor-acceptor type were formed, and that at temperatures of 15°C and less the stoichiometry of these was greater than 1:1. The procedures described are compared with those used in other donor-acceptor studies, and the results observed from the equilibrium studies are interpreted by using data reported for other sulfur dioxide-donor systems.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2691-2701 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cohesive films of a series of chromium(III) tris(phosphinates)[Cr(OPRR′O)(OPR″-R‴O)(OPR*R**O)]y in which the side groups on the phosphorus are alkyl, phenyl, and/or hydrogen groups have been prepared by reaction casting or by hot pressing. The preparative reaction appears to involve conversion of an aquahydroxo or hydroxo chromium(III) bis(phosphinate) to an intermediate hydroxo bis(phosphinate) containing coordinated phosphinic acid followed by an intrachain reaction leading to the tris(phosphinate). Tensile strengths of the chromium(III) tris(phosphinates) range from 100 to 5600 psi, elongations from less than 1 to 100%. Thermogravimetric data indicate that major decomposition occurs at temperatures from 200 to 435°C in air and from 410 to 510°C in nitrogen. Infrared spectra and physical properties are interpreted to support a structure for the chromium(III) tris(phosphinates) which is based on linear, triple-bridged chains. The presence of octyl or other long alkyl side groups on the phosphorus improves the physical properties, presumably by internal plasticization, but leads to decreased thermal stability.
    Additional Material: 2 Ill.
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