Abstract
During the period from 1975 to 1985, a variety of joint replacement prostheses were introduced clinically that included a bearing surface of titanium-6% alumi-num-4% vanadium alloy (Ti-6A1-4V) articulating against an acetabular component of ultra-high molecular weight (UHMW) polyethylene. Hip prostheses included the STH, the DF-80, the Six Ti-28 and the Six Ti-32 (Zimmer, Inc. Warsaw, IN), the Stanmore (Zimmer GB), the ES-30 (Biomet, Inc., Warsaw, IN) and the APR (Intermedics, Inc., Austin, TX). Titanium alloy knee prostheses included the Miller/Galante (Zimmer) and the Natural Knee (Intermedics). The suitability of this combination of bearing materials was initially questioned because, in some laboratory wear tests, titanium alloy underwent severe abrasive-corrosive wear, characterized by extensive scoring of the metal surface and the release of large amounts of finely divided metallic particles that blackened the opposing polymer and the lubricant [1-8].
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McKellop, H.A., Rostlund, T., Ebramzadeh, E., Sarmiento, A. (2001). Wear of Titanium 6–4 Alloy in Laboratory Tests and in Retrieved Human Joint Replacements. In: Titanium in Medicine. Engineering Materials. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56486-4_22
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DOI: https://doi.org/10.1007/978-3-642-56486-4_22
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