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  • Polymer and Materials Science  (18)
  • 1995-1999  (14)
  • 1960-1964  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2299-2310 
    ISSN: 0887-624X
    Keywords: plasma ; x-ray photoelectron spectroscopy surface modification ; O3P ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase downstream products of an air glow discharge have been measured, using absorption and emission spectroscopies, as a function of plasma power, air flow rate, and distance from the plasma. In addition, the reaction of these products with a linear low density polyethylene (LLDPE) polymer surface has been followed using x-ray photoelectron spectroscopy (XPS). At higher air flow rates (〉300 sccm), the primary reactive species is confirmed to be O(3P) atomic oxygen. Some O(3P) is generated in the plasma itself, but more appears to be formed in the downstream region, because of dissociation of molecules in their excited states. At low flow rates, the concentration of O(3P) is strongly depleted at the sample position, but other atomic oxygen states become more prominent. O(5S) and O(3S) are two states which are identified. XPS studies of the polyethylene surface reacted at high flow rates shows oxygen functionalities that are likely the result of an initiation by hydrogen abstraction. At low flow rates, the products suggest initiation by oxygen insertion. Thus, changes in flow rate can result in major changes to the polymer surface chemistry. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1015-1023 
    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: Bales of antioxidant-stabilized guayule rubber underwent significant losses in bulk viscosity when stored under ambient conditions at an Arizona processing facility. Previous work implicated the unsaturated fatty acid esters present in entrained resin as promoters of such degradation. Aging studies as functions of storage temperature and unsaturated acid ester content were carried out on both bulk rubber and rubber-resin solution (miscella) for cultivar AZ-101. The rate of thermooxidative degradation, determined as a function of Mooney viscosity, was increased by the addition of unsaturated ester. Anaerobic degradation was not affected in this way. The activation energy of chain thermolysis was found to be 116 ± 6 kJ/mol (28 ± 1 kcal/mol). At temperatures above 60°C, chain recombination successfully competed with chain scission in lower viscosity rubber. The rate of thermoox-idative degradation was substantially higher in a typical process miscella. A hindered amine antioxidant significantly reduces chain scission under these conditions. © 1996 John Wiley & Sons, Inc.
    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 5 (1961), S. 195-202 
    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 temperature dependence of the viscous component E2(1/T) of the dynamic modulus is reported for a homologous series of butadiene-styrene copolymers incorporated at various levels in styrene homopolymer. By the use of a vibrating reed technique based on resonance tuning, the frequency of the applied deformation was maintained essentially constant throughout the temperature range which included the glass transitions of the copolymers. It is shown that, when E2(1/T) for such mixed polymer systems is plotted against reciprocal absolute temperature, the area under the peak corresponding to a given copolymer affords a direct measure of the quantity of the copolymer present. Further, the temperature of maximum E2(1/T) is related to the mole fraction of bound styrene in the copolymer, and the shape of the peak is related to the statistical sequence lengths of styrene and butadiene in the copolymer.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1291-1306 
    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 temperature dependence at constant frequency of the viscous component E2(1/T) of the dynamic modulus has been determined for a homologous series of butadiene-acrylonitrile copolymers supported in a matrix of styrene homopolymer. The results, which agree with those reported earlier for a homologous series of butadiene-styrene copolymers, indicate that the transition temperature of a given plastic homopolymer, as measured from dynamic mechanical properties at essentially constant frequency in the range 200-300 cycles/sec., is depressed by the presence of a copolymerized rubbery diluent as the melting point of crystalline polymers is depressed by the presence of noncrystallizing comonomers. In addition, it has been found that the transition temperature is depressed by the presence of monomeric diluents much as the melting point of crystalline polymers is depressed by the presence of monomeric diluents. Two earlier assumptions, that the dynamic properties in the frequency range of interest should be independent of both the molecular weight of the rubbery copolymer and the degree of dispersion of the copolymer in the thermoplastic matrix, have been subjected to experimental scrutiny. The assumption regarding the dependence on molecular weight has been substantiated, at least for DP's in excess of 100. The assumption regarding the dependence on the degree of dispersion has been negated; the area under the E2(1/T) peak was found to be considerably greater for a coarse dispersion than for a fine one.
    Additional Material: 10 Ill.
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  • 5
    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
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 873-878 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A mass-separated low-energy ion beam system was used to deliver pure OH+ and NH+ to 15nm thick polystyrene films on silicon in ultrahigh vacuum. This was done in an effort to produce specific surface chemical functional groups. X-ray photoelectron spectroscopy showed that when the bombardment energy of OH+ exceeded 10 eV, or the dose was higher than 1 × 1016 ions cm-2, a mixture of C—OH, C—C=O and C—COOH groups was produced, along with severe damage to the aromatic rings. However, for bombardment at 10 eV with a dose of 1 × 1016 ions cm-2, only C—OH (or COR) groups were found. Similarly, bombardment with NH+ at 10 eV and a dose 1 × 1016 ions cm-2 induced incorporation of a single nitrogen-containing functionality. The C 1s data indicated that the major chemical functionality on such surfaces in a C—NH2 (or C—NHR) group with a minor component of C—(NH2)2. Hence, surface functionality can indeed be controlled by altering the molecular nature, energy and dose of the bombarding species.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 788-789 
    ISSN: 0142-2421
    Keywords: SIMS ; topography ; AFM ; imaging ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: In order to provide an accurate rendition of a three-dimensional (3D) volume obtained by SIMS, it is necessary to take account of the topography of the original surface and the relative sputter rates of the different structures within the volume. We describe a method that corrects both distortions to 3D SIMS images. An atomic force microscope is used to produce a topographic images of the area analysed by SIMS, both before and after the depth profile. This information is convoluted with the 3D SIMS image to produce a correct 3D image of the changes in composition within the volume of the material. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 573-580 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Factor analysis (FA), the multivariate statistical technique, has been used to extract chemical bonding information from SIMS secondary ion energy distributions. The method is outlined in detail and shown to be capable of constructing quantitative profiles for the chemical states of zirconium present in ZrO2/Zr and ZrNx/Zr structures. In addition, a truncated data collection procedure wherein secondary ion intensity values are collected at a fixed number of emission energy values during the depth profile is outlined. This method, which enables data to be collected in a shorter time and from a smaller sample volume, is subsequently shown to yield reliable results, as confirmed by FA of Auger depth profiles on similar specimens.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 163-170 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: This report illustrates, in a stepwise fashion, the application of a new method for quantifying SIMS results (termed the infinite velocity method) to the depth profile analysis of multilayered samples. The two samples analysed comprised a silicon substrate implanted with cobalt and a silicon substrate bearing an oxide layer implanted with boron. Concentrations were extracted by: sampling the secondary ion emissions over several kinetic energies during the depth profile; correcting the resulting intensities for instrument transmission and sputter yield effects, so that these may be poltted against the inverse of the velocity; and referencing the point at which the resulting curves intersect with the intensity axis (intensity at infinite velocity) to an element whose concentration is known, or to the sum of all major element intercept data. Characteristic velocity data obtained from each cycle of the depth profiles were also used to illustrate a new method for defining the position of the interface. To illustrate the validity of these results, peak concentrations were compared with those calculated via the integration method as well as Auger depth profile analysis.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 529-530 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: No Abstract
    Additional Material: 2 Ill.
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