Carbonitride precipitation in niobium/vanadium microalloyed steels
Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichio...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Speer, J. G. [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1987 |
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| Schlagwörter: |
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| Anmerkung: |
© The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 |
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| Übergeordnetes Werk: |
Enthalten in: Metallurgical and materials transactions / A - Springer New York, 1994, 18(1987), 2 vom: 01. Feb., Seite 211-222 |
|---|---|
| Übergeordnetes Werk: |
volume:18 ; year:1987 ; number:2 ; day:01 ; month:02 ; pages:211-222 |
| Links: |
|---|
| DOI / URN: |
10.1007/BF02825702 |
|---|
| Katalog-ID: |
OLC2053958707 |
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| 520 | |a Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. | ||
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10.1007/BF02825702 doi (DE-627)OLC2053958707 (DE-He213)BF02825702-p DE-627 ger DE-627 rakwb eng 670 530 VZ 19,1 ssgn Speer, J. G. verfasserin aut Carbonitride precipitation in niobium/vanadium microalloyed steels 1987 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel Michael, J. R. aut Hansen, S. S. aut Enthalten in Metallurgical and materials transactions / A Springer New York, 1994 18(1987), 2 vom: 01. Feb., Seite 211-222 (DE-627)171342011 (DE-600)1179415-X (DE-576)038876930 1073-5623 nnns volume:18 year:1987 number:2 day:01 month:02 pages:211-222 https://doi.org/10.1007/BF02825702 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY AR 18 1987 2 01 02 211-222 |
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10.1007/BF02825702 doi (DE-627)OLC2053958707 (DE-He213)BF02825702-p DE-627 ger DE-627 rakwb eng 670 530 VZ 19,1 ssgn Speer, J. G. verfasserin aut Carbonitride precipitation in niobium/vanadium microalloyed steels 1987 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel Michael, J. R. aut Hansen, S. S. aut Enthalten in Metallurgical and materials transactions / A Springer New York, 1994 18(1987), 2 vom: 01. Feb., Seite 211-222 (DE-627)171342011 (DE-600)1179415-X (DE-576)038876930 1073-5623 nnns volume:18 year:1987 number:2 day:01 month:02 pages:211-222 https://doi.org/10.1007/BF02825702 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY AR 18 1987 2 01 02 211-222 |
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10.1007/BF02825702 doi (DE-627)OLC2053958707 (DE-He213)BF02825702-p DE-627 ger DE-627 rakwb eng 670 530 VZ 19,1 ssgn Speer, J. G. verfasserin aut Carbonitride precipitation in niobium/vanadium microalloyed steels 1987 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel Michael, J. R. aut Hansen, S. S. aut Enthalten in Metallurgical and materials transactions / A Springer New York, 1994 18(1987), 2 vom: 01. Feb., Seite 211-222 (DE-627)171342011 (DE-600)1179415-X (DE-576)038876930 1073-5623 nnns volume:18 year:1987 number:2 day:01 month:02 pages:211-222 https://doi.org/10.1007/BF02825702 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY AR 18 1987 2 01 02 211-222 |
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10.1007/BF02825702 doi (DE-627)OLC2053958707 (DE-He213)BF02825702-p DE-627 ger DE-627 rakwb eng 670 530 VZ 19,1 ssgn Speer, J. G. verfasserin aut Carbonitride precipitation in niobium/vanadium microalloyed steels 1987 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel Michael, J. R. aut Hansen, S. S. aut Enthalten in Metallurgical and materials transactions / A Springer New York, 1994 18(1987), 2 vom: 01. Feb., Seite 211-222 (DE-627)171342011 (DE-600)1179415-X (DE-576)038876930 1073-5623 nnns volume:18 year:1987 number:2 day:01 month:02 pages:211-222 https://doi.org/10.1007/BF02825702 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY AR 18 1987 2 01 02 211-222 |
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10.1007/BF02825702 doi (DE-627)OLC2053958707 (DE-He213)BF02825702-p DE-627 ger DE-627 rakwb eng 670 530 VZ 19,1 ssgn Speer, J. G. verfasserin aut Carbonitride precipitation in niobium/vanadium microalloyed steels 1987 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel Michael, J. R. aut Hansen, S. S. aut Enthalten in Metallurgical and materials transactions / A Springer New York, 1994 18(1987), 2 vom: 01. Feb., Seite 211-222 (DE-627)171342011 (DE-600)1179415-X (DE-576)038876930 1073-5623 nnns volume:18 year:1987 number:2 day:01 month:02 pages:211-222 https://doi.org/10.1007/BF02825702 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY AR 18 1987 2 01 02 211-222 |
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| author |
Speer, J. G. |
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Speer, J. G. ddc 670 ssgn 19,1 misc Austenite misc Metallurgical Transaction misc Rolling Reduction misc Steel Composition misc Microalloyed Steel Carbonitride precipitation in niobium/vanadium microalloyed steels |
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670 530 VZ 19,1 ssgn Carbonitride precipitation in niobium/vanadium microalloyed steels Austenite Metallurgical Transaction Rolling Reduction Steel Composition Microalloyed Steel |
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ddc 670 ssgn 19,1 misc Austenite misc Metallurgical Transaction misc Rolling Reduction misc Steel Composition misc Microalloyed Steel |
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ddc 670 ssgn 19,1 misc Austenite misc Metallurgical Transaction misc Rolling Reduction misc Steel Composition misc Microalloyed Steel |
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Carbonitride precipitation in niobium/vanadium microalloyed steels |
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Carbonitride precipitation in niobium/vanadium microalloyed steels |
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Speer, J. G. |
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Metallurgical and materials transactions / A |
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1987 |
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211 |
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Speer, J. G. Michael, J. R. Hansen, S. S. |
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10.1007/BF02825702 |
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670 530 |
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carbonitride precipitation in niobium/vanadium microalloyed steels |
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Carbonitride precipitation in niobium/vanadium microalloyed steels |
| abstract |
Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 |
| abstractGer |
Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 |
| abstract_unstemmed |
Abstract A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe−Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954°C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843°C, 954°C, or 1066°C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix precipitates are consistently more niobium-rich than predicted by the model. © The Metallurgical Society of American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc., and American Society for Metals 1987 |
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Carbonitride precipitation in niobium/vanadium microalloyed steels |
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