Microstructural development during the quenching and partitioning process in a newly designed low-carbon steel

被引:318
作者
Santofimia, M. J. [1 ,2 ]
Zhao, L. [1 ,2 ]
Petrov, R. [1 ,3 ]
Kwakernaak, C. [1 ]
Sloof, W. G. [1 ]
Sietsma, J. [1 ]
机构
[1] Delft Univ Technol, Dept Mat Sci & Engn, NL-2628 CD Delft, Netherlands
[2] M2i, NL-2628 CD Delft, Netherlands
[3] Univ Ghent, Dept Met & Mat Sci, B-9052 Ghent, Belgium
关键词
Steels; Microstructure; Phase transformations; INTERFACE MIGRATION; BAINITIC STEELS; TRIP STEELS; P PROCESS; MARTENSITE; AUSTENITE; TRANSFORMATION;
D O I
10.1016/j.actamat.2011.06.014
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This paper presents a detailed characterization of the microstructural development of a new quenching and partitioning (Q&P) steel. Q&P treatments, starting from full austenitization, were applied to the developed steel, leading to microstructures containing volume fractions of retained austenite of up to 0.15. The austenite was distributed as films in between the martensite laths. Analysis demonstrates that, in this material, stabilization of austenite can be achieved at significantly shorter time scales via the Q&P route than is possible via a bainitic isothermal holding. The results showed that the thermal stabilization of austenite during the partitioning step is not necessarily accompanied by a significant expansion of the material. This implies that the process of carbon partitioning from martensite to austenite occurs across low-mobility martensite-austenite interfaces. The amount of martensite formed during the first quench has been quantified. Unlike martensite formed in the final quench, this martensite was found to be tempered during partitioning. Measured volume fractions of retained austenite after different treatments were compared with simulations using model descriptions for carbon partitioning from martensite to austenite. Simulation results confirmed that the carbon partitioning takes place at low-mobility martensite-austenite interfaces. (C) 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6059 / 6068
页数:10
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