Compositional analysis on the reverted austenite and tempered martensite in a Ti-stabilized supermartensitic stainless steel: Segregation, partitioning and carbide precipitation

被引:56
|
作者
Escobar, J. D. [1 ,2 ,3 ]
Poplawsky, J. D. [4 ]
Faria, G. A. [3 ]
Rodriguez, J. [1 ]
Oliveira, J. P. [3 ]
Salvador, C. A. F. [2 ]
Mei, P. R. [2 ]
Babu, S. S. [5 ,6 ]
Ramirez, A. J. [3 ]
机构
[1] CNPEM, LNNano, Brazilian Nanotechnol Natl Lab, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Univ Campinas, FEM, Coll Mech Engn, BR-13083860 Campinas, SP, Brazil
[3] Ohio State Univ, Dept Mat Sci & Engn, Welding Engn, 1248 Arthur E Adams Dr, Columbus, OH 43221 USA
[4] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[5] Univ Tennessee, Mech Aerosp & Biomed Engn, Knoxville, TN 37996 USA
[6] Oak Ridge Natl Lab, Mfg Demonstrat Facil, Knoxville, TN USA
基金
巴西圣保罗研究基金会;
关键词
Atom probe tomography; Austenite reversion; Isothermal tempering treatments; Synchrotron diffraction; X-RAY-DIFFRACTION; ATOM-PROBE TOMOGRAPHY; RETAINED AUSTENITE; IN-SITU; TRANSFORMATION MECHANISM; GRAIN-BOUNDARIES; MULTIPASS WELDS; HEAT-TREATMENT; TRIP STEELS; MICROSTRUCTURE;
D O I
10.1016/j.matdes.2017.11.055
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Controlling the amount of reverted austenite at room temperature allows for tailoring of mechanical properties in supermartensitic stainless steels. The austenite reversion and stabilization occurs during inter-critical tempering through partitioning of austenite-stabilizing elements. The degree of partitioning greatly depends on the reversion temperature, which dictates the local equilibrium conditions. Atom probe tomography and energy dispersive spectroscopy in transmission electron microscopy were used to study the austenite reversion mechanism in terms of the elemental distribution of austenite-stabilizing, ferrite-stabilizing and carbide forming elements. Synchrotron X-ray diffraction confirmed that the austenite equilibrium phase fraction was reached after 2.5 h of isothermal reversion at 625 degrees C, allowing for direct comparison with thermodynamic and kinetic calculations. However, such soaking time was not enough to produce compositional homogenization in the reverted austenite. The austenite reversion and stabilization mechanism was related mainly to strong partitioning of Ni. Negligible partitioning of Cr, Mo, Si and Ti were observed. Instead, these elements were strongly segregated at the reverted austenite/martensite interfaces. Carbon and Ti played a secondary role in the austenite stabilization through the precipitation of nano-sized Ti (C, N) with partial substitution of Ti by Mo. Virtually carbon-free austenite and martensite were observed away from the interfaces and precipitates. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:95 / 105
页数:11
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