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Acta Metall Sin  2020, Vol. 56 Issue (10): 1335-1342    DOI: 10.11900/0412.1961.2020.00002
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Peritectic Solidification Characteristics and Mechanism of 15CrMoG Steel
LI Yaqiang1, LIU Jianhua1(), DENG Zhenqiang1, QIU Shengtao2, ZHANG Pei3, ZHENG Guiyun3
1 Institute of Engineering Technology, University of Science and Technology Beijing, Beijing 100083, China
2 National Engineering Research Center of Continuous Casting Technology, Central Iron and Steel Research Institute, Beijing 100081, China
3 Laiwu Branch of Shandong Iron and Steel Ltd. , Jinan 271104, China
Cite this article: 

LI Yaqiang, LIU Jianhua, DENG Zhenqiang, QIU Shengtao, ZHANG Pei, ZHENG Guiyun. Peritectic Solidification Characteristics and Mechanism of 15CrMoG Steel. Acta Metall Sin, 2020, 56(10): 1335-1342.

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Abstract  

Cast defects of hypo-peritectic steel such as uneven growth of strand shell, crack formation and oscillation marks formation were found to occur frequently during continuous casting of steels. In industry, measures such as high-basicity casting powder, hot-top mold and reduction of mold cooling strength were usually used in the investigations, but a reasonable explanation for these measures has been lacking. In this work, solidification of 15CrMoG steel at different cooling rates were observed with an ultra high temperature confocal scanning laser microscope. The precipitation of the δ-phase was in a cellular manner when the cooling rates were 5 and 15 ℃/min, whereas it was in a dendrite manner when the cooling rate was increased to 100 ℃/min. Thermodynamic analysis of the peritectic phase nucleation showed that a concentration gradient existed at the L/δ interface during the solidication of initial δ phase which led to an increase in the Gibbs free energy barrier for the nucleation of the peritectic γ phase. As the cooling rate increased, the concentration gradient across the L/δ interface became steeper, resulting in an increase in the nucleation undercooling of the peritectic γ phase. This, in turn, decreased the temperature and increased the peritectic reaction rate. In addition, an increase in the cooling rate led to a change in the mode of peritectic transformation (δγ). A diffusion-controlled δγ transformation occurred due to the progression of planar and cellular interfaces at cooling rates of 5 and 15 ℃/min, respectively. However, a large δγ transformation, which was controlled by the interface process, occurred when the cooling rate was increased to 100 ℃/min. The difference in volume shrinkage of the different modes of peritectic transformation (δγ) led to a discussion of the control mechanism of continuous casting of hypo-peritectic steel.

Key words:  15CrMoG steel      cooling rate      peritectic reaction      peritectic transformation      continuous casting     
Received:  02 January 2020     
ZTFLH:  TF777  
Fund: National Natural Science Foundation of China(51874028)

URL: 

https://www.ams.org.cn/EN/10.11900/0412.1961.2020.00002     OR     https://www.ams.org.cn/EN/Y2020/V56/I10/1335

Fig.1  Schematic of temperature control of experiments
Fig.2  In situ observations of δ precipitation and peritectic phase transformation at a cooling rate of 5 ℃/min (L—liquid phase)
(a, b) precipitation and growth of δ-ferrite (c, d) peritectic reaction (e, f) peritectic transformation
Fig.3  In situ observations of δ precipitation and peritectic phase transformation at the cooling rate of 15 ℃/min (a, b) precipitation and growth of δ-ferrite (c, d) peritectic reaction (e, f) peritectic transformation
Fig.4  In situ observations of δ precipitation and peritectic phase transformation at the cooling rate of 100 ℃/min
(a, b) precipitation and growth of δ-ferrite (c, d) peritectic reaction (e, f) peritectic transformation
Fig.5  Peritectic reactions at cooling rates of 5 ℃/min (a), 15 ℃/min (b) and 100 ℃/min (c)
Fig.6  Peritectic transformations at cooling rates of 5 ℃/min (a), 15 ℃/min (b) and 100 ℃/min (c)
Fig.7  Schematic of the concentration distribution at theL/δ interface
Fig.8  Carbon concentration distribution (a) and Gibbs free energies at cooling rates of 5 ℃/min (b), 15 ℃/min (c) and 100 ℃/min (d), respectively (T1, T2 and T3 are peritectic phase transformation temperatures at cooling rates of 5, 15 and 100 ℃/min, respectively. T0-line is the thermodynamic equivalence of δ and γ. Gδm, Gγmand GLm are Gibbs free energies of δ, γ and liquid, respectively. ΔGm is the thermodynamic driving force for the transformation of δ to γ. Cδ* is interfacial composition of δ. Cδe, Cγ/δe, Cγ/Leand CLe are the average compositions of δ,γ/δ interface, γ/L interface and liquid, respectively)
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Fig.9  Migration distances of the L/δ and δ/γ interfaces as a function of the square root of time at the cooling rate of 5 ℃/min (t—time)
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