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  • 1995-1999  (2)
  • 1960-1964  (2)
Material
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Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 29 (1964), S. 2799-2800 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 29 (1964), S. 2682-2685 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 32 (1997), S. 4909-4916 
    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 Barrier-type film growth on the high strength aluminium alloy FVS0812 has been studied by a combination of transmission electron microscopy and Rutherford backscattering spectroscopy. The film is composed mainly of amorphous anodic alumina, but is contaminated with iron species incorporated into the film from the alloy. The film may also be contaminated with silicon and vanadium species at levels below the detection limit of the present experiments. The contaminant species are primarily incorporated locally into the film during oxidation of Al13(Fe, V)3Si dispersoids and the resulting film material is of reduced resistivity compared with anodic alumina of high purity. As a consequence of the presence of regions of film material of differing resistivities, the film is of irregular thickness. The average thickness corresponds to a nm/V ratio of about 1.3. Iron species incorporated into the film migrate outwards at roughly 2.1 times the rate of Al3+ ions. The iron species are not ejected in significant amounts to the electrolyte on reaching the film/electrolyte interface and hence, a thin layer of film material highly enriched in iron species develops at the film surface. The layer may also be enriched in vanadium species, if these are incorporated into the film and migrate more rapidly than Al3+ ions. Enrichment of iron, and possibly other alloying element atoms, is found in a thin layer of alloy immediately beneath the anodic film, paralleling enrichments of alloying element atoms found following anodic oxidation of other aluminium alloys. The enrichments at both the alloy/film and film/electrolyte interfaces do not appear to be continuous across the macroscopic surface of the specimens, probably due to the non-uniformity of film growth on the two-phase substrate. The maximum voltage for the selected conditions of anodizing was limited to 68 V as a result of oxygen generation at flaws which are present extensively in the anodic film.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 33 (1998), S. 4159-4165 
    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 The formation of porous anodic films on FVS0812 aluminium alloy has been examined by transmission electron microscopy in order to elucidate the processes of film growth. A complex morphology of film material is revealed containing relatively tortuous, branched and terminated porosity and relatively large cavities. The morphology is associated with the differing anodic oxidation behaviour of the aluminium matrix and silicide dispersion regions of the alloy and the differing chemical stabilities of the resultant film regions. The anodic oxidation of the silicide proceeds more slowly than that of the aluminium matrix, with the production of film material of much finer morphology. The reduced rate of oxidation of the silicide is attributed to the effects of alloying element species in the anodic film material and pore solution. The rate of oxidation of the silicide is sufficient for most of the particles to be oxidized completely during anodizing. However, the resultant film material subsequently dissolves in the pore solution leaving relatively large cavities in the film. The differing oxidation rates of the alloy components, coupled with locally differing film properties, leads to a relatively rough alloy/film interface.© 1998 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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