Phase instabilities and carbon additions in single-crystal nickel-base superalloys
Creators
Description
The phase stability of a number of experimental single-crystal nickel-base superalloys with elevated levels of rhenium, tungsten and tantalum (Ta) has been studied. Carbon additions of 0.1 wt.% were found to enhance the phase stability of the as-cast alloys, with respect to inhibiting the formation of topologically close-packed (TCP) phases. In addition to forming a variety of primary Ta-rich MC carbides upon solidification, intentional carbon additions also affected the segregation behavior of the constituent refractory elements. Comparison of experimentally measured distribution coefficients assessed via application of a Scheil-type analyses revealed reduced segregation of the refractory elements associated with precipitation of TCP phases in the carbon-containing alloys
Additional details
Identifiers
- DOI
- 10.1016/S0921-5093(02)00637-8;
- arXiv
- arXiv:hep-th/9706196v3;
- PII
- S0921509302006378;
Publishing Information
- Journal Title
- Materials Science and Engineering. A, Structural Materials: Properties, Microstructure and Processing
- Journal Volume
- 348
- Journal Issue
- 1-2
- Journal Page Range
- p. 111-121
- ISSN
- 0921-5093
- CODEN
- MSAPE3
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38069924
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBIDES; CARBON; CARBON ADDITIONS; COMPARATIVE EVALUATIONS; DISTRIBUTION; HEAT RESISTING ALLOYS; INSTABILITY; MONOCRYSTALS; NICKEL; PHASE STABILITY; PRECIPITATION; REFRACTORIES; RHENIUM; SEGREGATION; SOLIDIFICATION; TANTALUM; TCP; TUNGSTEN
- Descriptors DEC
- ALLOYS; CARBON COMPOUNDS; CRYSTALS; ELEMENTS; ESTERS; EVALUATION; HEAT RESISTANT MATERIALS; MATERIALS; METALS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC PHOSPHORUS COMPOUNDS; PHASE TRANSFORMATIONS; PHOSPHORIC ACID ESTERS; REFRACTORY METALS; SEPARATION PROCESSES; STABILITY; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2002 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.