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The Substructure of Austenite and Martensite Through a Carburized Surface

Published online by Cambridge University Press:  06 March 2019

J. D. Makinaon
Affiliation:
Department of Mechanical Engineering Center for Materials Research and Analysis University of Nebraska-Lincoln Lincoln, NE 68588-0656
W. N. Weins
Affiliation:
Department of Mechanical Engineering Center for Materials Research and Analysis University of Nebraska-Lincoln Lincoln, NE 68588-0656
R. J. De Angelis
Affiliation:
Department of Mechanical Engineering Center for Materials Research and Analysis University of Nebraska-Lincoln Lincoln, NE 68588-0656
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Abstract

The complex relationships among composition, roartensite start and finish temperatures, morphology of the martensite, residual stress distribution, and quenching conditions produce significant microstructural changes through a carburized case. Variations in the amount of retained austenite, the diffracting-particle size, and hardness were measured every 50μm in depth through a one percent carbon case on AISI-SAE 4320 steel. Measurement were made to a total depth of 2 mm. The percent retained austenite decreases from a maximum of 26% near the surface to a few percent in the bulk. It is shown that the x-ray diffracting-particle size of the martenaite phase is a structure parameter that changes when the martensite morphology goes from plate to lath type. The austenite phase diffracting-particle size is controlled hy the deformatioxis induced by the martensite formation.

Type
X. Crystallite Size/Strain Analysis
Copyright
Copyright © International Centre for Diffraction Data 1990

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References

[1] Jatczak, C. F., “Retained Austenite and its Measurement by X-Ray Diffraction,” SAE, Warrendale, PA 1980.Google Scholar
[2] “Metals Handbook, Properties and Selection: Iron and Steels,” 9th ed, ASM, Materials Park, OH 1985.Google Scholar
[3] “International Tables for X-Ray Crystallography,” v3, Kynoch, Birmingham, 1969.Google Scholar
[4] Cullity, B. D., “Elements of X-Ray Diffraction,” 2nd Ed. Addison Wesley 1978.Google Scholar
[5] DeAngelis, R. J., Dhere, A., Lewis, J., Kuo, H., “Techniques to Study the Sintering of Catalysts”, Sintering and Heterogeneous Catalysis, p.181, Plenum, 1984.Google Scholar
[6] Warren, B. E., “X-Ray Diffraction,” Addison Wesley 1969.Google Scholar
[7] Severdenko, V. P. et al. X-ray Diffraction Analysis of Stacking Faults in the Residual Austenite of Cr-W Steel 5Kh2VMNF After Low- Temperature Thermomechanical Treatment, Izvest. Akad. Nauk Beloruss. SSR.1975.Google Scholar