Strengthening mechanisms of carbon in modified nickel-based superalloy Nimonic 80A
- 1. Institute of Materials, Shanghai University, Shanghai 200072 (China)
- 2. Baoshan Iron and Steel Co., Ltd., Shanghai 200940 (China)
- 3. Shanghai Electric Power Generation Equipment Co., Ltd., Turbine Works 200240 (China)
Description
Highlights: → Misfit δ between γ' and γ phases increased with the increase of carbon content. → Cr23C6 has an orientation relationship with the γ matrix for the 0.10%C alloy. → Cr23C6 at grain boundary enhance the grain boundary strengthening. → Dislocation networks and precipitate strengthening benefit stress-rupture properties. - Abstract: Nickel-based superalloy Nimonic 80A with various carbon contents has been developed. Various strengthening mechanisms of carbon were analyzed by optical microscope, X-ray diffraction, scanning electron microscope equipped with energy dispersive spectroscopy and transmission electron microscope. Detailed microstructural analysis revealed that with the increase of carbon content from 0.01% to 0.10%, both the lattice parameters of γ' and γ phases decreased, and the misfit δ between the coherent γ' and γ phases increased slightly from 0.289% to 0.317% after full heat treatment at 1070 deg. C/8 h, A.C. + 700 deg. C/16 h, A.C. The diameter of spherical γ' phase decreased from 22.24 nm of 0.01%C alloy to less than 15.76 nm of 0.06%C and 0.10%C alloys. Cr23C6 carbide precipitated at the grain boundary in the alloys with carbon content higher than 0.06%, and when carbon content increased to 0.10%, Cr23C6 carbide had an orientation relationship with the γ matrix: [001-bar] Cr23C6-parallel [001-bar]γmatrixand(100)Cr23C6-parallel (1 0 0) γ matrix, which can enforce the grain boundary strength. The growth of room temperature tensile strength with the increase of carbon content was primarily due to the coherent strain strengthening and the precipitate strengthening of Cr23C6 carbide. After stress-rupture test at 750 deg. C/310 MPa, the misfit δ increased from 0.182% to 0.237% with the increase of carbon content, but the values were lower than those after full heat treatment. The precipitate of blocky Cr23C6 in 0.10%C alloy tended to become spherical and dislocation lines were found in the γ matrix channels between γ' phases, the combination of the dislocation strengthening and precipitate strengthening of Cr23C6 carbide at grain boundary was beneficial to the stress-rupture properties.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msea.2011.02.072Additional details
Identifiers
- DOI
- 10.1016/j.msea.2011.02.072;
- PII
- S0921-5093(11)00247-4;
Publishing Information
- Journal Title
- Materials Science and Engineering. A, Structural Materials: Properties, Microstructure and Processing
- Journal Volume
- 528
- Journal Issue
- 13-14
- Journal Page Range
- p. 4600-4607
- ISSN
- 0921-5093
- CODEN
- MSAPE3
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44010467
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBON; CHROMIUM CARBIDES; DISLOCATIONS; GRAIN BOUNDARIES; HEAT TREATMENTS; LATTICE PARAMETERS; MATRIX MATERIALS; NIMONIC 80A; ORIENTATION; PRECIPITATION; RUPTURES; SCANNING ELECTRON MICROSCOPY; SPECTROSCOPY; STRAINS; STRESSES; TENSILE PROPERTIES; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION
- Descriptors DEC
- ALLOY-NI76CR20TI2; ALLOYS; ALUMINIUM ALLOYS; BORON ADDITIONS; BORON ALLOYS; CARBIDES; CARBON COMPOUNDS; CHROMIUM ALLOYS; CHROMIUM COMPOUNDS; COHERENT SCATTERING; CORROSION RESISTANT ALLOYS; CRYSTAL DEFECTS; CRYSTAL STRUCTURE; DIFFRACTION; ELECTRON MICROSCOPY; ELEMENTS; FAILURES; HEAT RESISTANT MATERIALS; HEAT RESISTING ALLOYS; LINE DEFECTS; MATERIALS; MECHANICAL PROPERTIES; MICROSCOPY; MICROSTRUCTURE; NICKEL ALLOYS; NICKEL BASE ALLOYS; NIMONIC; NONMETALS; SCATTERING; SEPARATION PROCESSES; TITANIUM ALLOYS; TRANSITION ELEMENT ALLOYS; TRANSITION ELEMENT COMPOUNDS; ZIRCONIUM ADDITIONS; ZIRCONIUM ALLOYS
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.