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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of food science & technology 19 (1984), S. 0 
    ISSN: 1365-2621
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The Super-scan meat analyser measures protein, fat and moisture on an homogenate of the sample by infrared absorption in the transmittance rather than the reflectance mode. A preliminary evaluation of the instrument using fifty-two samples of chicken or turkey meat indicated that the instrument gave reliable results for fat but not for protein and moisture. Regression equations were obtained from the combined data and used to correct the protein and moisture results. These equations were tested on a further twenty-eight samples of turkey meat and the results obtained demonstrated that the instrument could be used for the rapid analysis of poultry meat.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 5 (1986), S. 1133-1134 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 21 (1986), S. 2033-2042 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Isothermal oxidation experiments on WC powders revealed a systematic dependence of oxidation rate on powder particle size. Oxidation was followed by measuring the change in mass of the WC powder as WC is converted to WO3. Fine powders oxidized more quickly than coarse powders because for the same initial mass the fine powder had a larger surface area. Measurement of the change in mass with time were shown to resolve differences in mean size of 0.1 μm, and possibly less, between separate batches of powder. A theoretical expression for the change in mass with time of spherical particles has been derived which compares well with experimental measurements and which can also be used with appropriate assumptions to calculate the initial powder-size distribution.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 26 (1991), S. 1401-1408 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A powder sizing test developed for use on WC powders has been extended for use on iron and iron-neodymium-boron powders. In this test the particle size is derived from the rate of oxidation, because finer powders oxidize quicker. The rate of oxidation is monitored in a thermogravimetric analyser, where the powders are subjected to a controlled heating rate from room temperature to 1100 °C. If the constants from the Arrhenius law are known the powder size can be determined by comparing experimental oxidation plots with theoretical curves. For the sizing of a commercial spherical iron powder, the oxidation technique compared favourably with direct sizing using scanning electron microscopy and image analysis. The values for the activation energy of 125 kJ mol−1 determined in this study agree with previous studies. Validation of the sizing technique on a hydrogen-decrepitated stoichiometric Nd2Fe14B powder proved difficult because it was not possible to determine a definitive size distribution independently. Metallography of partially oxidized samples showed that the process is two-stage, at low temperatures the neodymium oxidizes, and above 400 °C the powder behaves as pure iron. Theoretical curves based on one oxidation process with an activation energy of 100 kJ mol−1 gave the best fit to the experimental curves.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 25 (1990), S. 296-310 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Two wear regimes were observed for a 95% alumina tested in dry sliding wear conditions using a pin on disc test geometry. Specimens prepared with lapped and polished surfaces exhibited low wear rates at applied loads of 10 and 40 N but ground surfaces wore rapidly at loads of 40 N and above. The surfaces that had experienced high wear rates contained more networks of microcracks and had rougher surface profiles than the mildly worn surfaces. X-ray line broadening analysis indicated that the wear debris had a particle size of 10 to 30 nm and contained plastic deformation, but no evidence of significant plastic deformation was found in the pin surfaces. Theoretical explanations are proposed for the existence of two types of wear behaviour: subsurface crack growth is believed to cause high wear rates, whilst low wear rates are due to a very fine scale abrasion of the surface. Recommendations are made on some of the precautions that should be taken to use alumina successfully in dry sliding wear applications.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 9 (1986), S. 55-63 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A scanning acoustic microscope (SAM) operating at 750 MHz has been used to image artificially induced cracks in polycrystalline and single crystal specimens of alumina. Although the resolution of the instrument used in this work, at 1.6m̈m, was not as good as that of an optical microscope, significantly more information about the crack characteristics was revealed acoustically. Cracks of finite width act as scattering points for acoustic waves and thus sources of contrast in the SAM image, even when their width is less than the theoretical spatial resolution. In polycrystalline samples it was found that defocussing the SAM both above and below the focal plane, utilising different regions of the V(z) response, enabled contrast due to grain boundaries, cracks, and individual grains to be distinguished. It was also possible to identify different modes of cracking. For the single crystal samples, distinctive contrast was obtained from both horizontal and vertical sub-surface cracks within one Rayleigh wavelength of the surface. In most materials, features such as these are not readily detectable by other techniques.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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