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  • 1
    ISSN: 1573-2711
    Keywords: solid lubricants ; lubricious oxides ; TiO2 ; rutile ; oxygen stoichiometry ; Magnéli phases ; tribometry ; friction ; wear ; shear strength ; temperature ; atmosphere ; extreme environment ; molecular engineering ; cation doping ; aliovalency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract As a follow-up to the work described in part I of this paper series, a preliminary study was conducted with polycrystalline rutile TiO−x to render its friction and wear performance independent of the environment. The main goal was to confine the most tribologically desirable oxygen stoichiometries of the crystallographic shear-induced Magnéli phases (CSMP) of rutile by doping with cations similar in size and polarizability to the Ti4+, but with lower valences. The resultant chemical expulsion of oxygen from the rutile lattice was intended to generate CSMP free of friction and wear variations caused by changes in the thermal–atmospheric environment. Copper, iron, cobalt and nickel ions were tried as dopants introduced as their stable oxides via a simple ball-milling, hot-pressing and annealing procedure, but only a (Ti + Cu)O1.80 model blend resulted in a desired reaction. A portion of the copper entered the lattice to form a new titanium–copper CSMP, resembling the well-known V3Ti6O17 catalyst equivalent to an undoped rutile CSMP with an O/Ti ratio of 1.89. Although the shear behavior of this new, wear-resistant compound was in accordance with predictions, its friction is higher and more variable than desired for a wide environmental regime lubricant. The preparation technique was only sufficient to demonstrate that oxygen vacancy-induced creation of low-friction CSMP may be possible by doping; it does not appear to be useful for formulating practical, rutile-based lubricious oxides.
    Type of Medium: Electronic Resource
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