Microstructural evolution during solution treatment of Co–Cr–Mo–C biocompatible alloys
- 1. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Rivadavia 1917, C1033AA, Buenos Aires (Argentina)
- 2. IFIMAT, Instituto de Física de Materiales Tandil, Facultad de Ciencias Exactas, Universidad Nacional del Centro de la Provincia de Buenos Aires, Pinto 399, B7000GHG Tandil (Argentina)
- 3. Comisión de Investigaciones Científicas de la Provincia de Buenos Aires (CICPBA), Calle 526 e/10 y 11, B1096APP, La Plata (Argentina)
Description
Three different Co–Cr–Mo–C alloys conforming to ASTM F75 standard were poured in an industrial environment and subjected to a conventional solution treatment at 1225 °C for several time intervals. The microstructural changes and transformations were studied in each case in order to evaluate the way in which treatment time influences the secondary phase fraction and clarify the microstructural changes that could occur. To assess how treatment time affects microstructure, optical microscopy and image analyzer software, scanning electron microscopy and energy dispersion spectrometry analysis were employed. The main phases detected in the as-cast state were: σ-phase, M6C, and M23C6 carbides. The latter presented two different morphologies, blocky type and lamellar type. Despite being considered the most detrimental feature to mechanical properties, σ-phase and lamellar carbides dissolution took place in the early stages of solution treatment. M23C6 carbides featured two different behaviors. In the alloy obtained by melting an appropriate quantity of alloyed commercial materials, a decrease in size, spheroidization and transformation into M6C carbides were simultaneously observed. In the commercial ASTM F75 alloy, in turn, despite being the same phase, only a marked decrease in precipitates size was noticed. These different behaviors could be ascribed to the initial presence of other phases in the alloy obtained from alloyed materials, such as σ-phase and "pearlitic" carbides, or to the initial precipitate size which was much larger in the first than in the commercial ASTM F75 alloy studied. M6C carbides dissolved directly in the matrix as they could not be detected in samples solution-treated for 15 min. - Highlights: ► Three different Co–Cr–Mo alloys were poured under an industrial environment. ► Transformation of existing phases followed during conventional solution treatment. ► In as-cast/treated samples, phases were identified by color metallography, SEM and EDS. ► M23C6 → M6C transformation was corroborated by SEM and EDS analysis. ► Carbide spheroidization was also detected prior a noticeably carbide size decreasing.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchar.2012.03.006Additional details
Identifiers
- DOI
- 10.1016/j.matchar.2012.03.006;
- PII
- S1044-5803(12)00063-0;
Publishing Information
- Journal Title
- Materials Characterization
- Journal Volume
- 68
- Journal Issue
- Complete
- Journal Page Range
- p. 49-57
- ISSN
- 1044-5803
- CODEN
- MACHEX
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44025770
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CHROMIUM CARBIDES; COBALT CARBIDES; MATRIX MATERIALS; MECHANICAL PROPERTIES; MELTING; METALLOGRAPHY; MICROSTRUCTURE; MOLYBDENUM CARBIDES; MORPHOLOGY; OPTICAL MICROSCOPY; SCANNING ELECTRON MICROSCOPY; SOLIDIFICATION; TRANSITION ELEMENT ALLOYS; X-RAY SPECTROSCOPY
- Descriptors DEC
- ALLOYS; CARBIDES; CARBON COMPOUNDS; CHROMIUM COMPOUNDS; COBALT COMPOUNDS; ELECTRON MICROSCOPY; MATERIALS; MICROSCOPY; MOLYBDENUM COMPOUNDS; PHASE TRANSFORMATIONS; REFRACTORY METAL COMPOUNDS; SPECTROSCOPY; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.