EUTECTIC CRYSTALLIZATION OF Fe-C ALLOYS WITH HYPERCEMENTITE CARBIDE

V. Mazur
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Abstract

Рurpose. To investigate the peculiarities of the structure formation in white cast irons with the participation of Fe3C and Fe7C3 carbides. Methods of research. By the comparing detailed both microscopic and thermal (DSC) kinetics of the melting and crystallization process to determine the regularities of the eutectic transformation of the white cast iron  under significant undercooling of the liquid phase. Microscopic analysis of samples using a light microscope Jenaphot 2000 (Carl Zeiss, Germany). Thermal analyses using differential scanning calorimeter (DSC) STA 449C “Jupiter” (Netzsch Geratebau GmbH, Germany). Results. It is shown that eutectic crystallization of white cast irons with great undercooling of the melt is a complex process that consists of crystallization and simultaneous dissolution of crystalline phases: γ austenite and two metastable carbides Fe3C and Fe7C3. In general, crystallization proceeds according to scheme L → L+ Fe7C3 +γ → L++ Fe7C3 + γ + Fe3C→ Fe7C3 +γ+ Fe3C. As a result, two eutectics are formed, one Fe7C3 +γ (plate-like) with austenitic, second ledeburite γ+ Fe3C with cementite matrix. Scientific novelty. The microscopic kinetics of nucleating and growth of plate-like Fe7C3 +γ eutectics was investigated and relative stability of Fe7C3 carbide under normal conditions was found. A scheme of metastable phase equilibria with the participation of Fe7C3 carbide in system Fe-Fe3C-Fe7C3 is proposed. Practical value. A simple liquid phase processing technology is proposed in order to generate significant undercooling of the melt that causes formation a natural composite material with both a matrix of transformed austenite and carbide reinforcing phases.
铁-碳合金与高碳体碳化物共晶
Рurpose。研究Fe3C和Fe7C3碳化物对白口铸铁组织形成的影响。研究方法。通过比较白口铸铁熔炼和结晶过程的微观和热动力学(DSC),确定了白口铸铁在液相明显过冷条件下共晶转变的规律。使用光学显微镜对样品进行显微分析Jenaphot 2000(卡尔蔡司,德国)。热分析使用差示扫描量热计(DSC) STA 449C“Jupiter”(德国Netzsch Geratebau GmbH)。结果。结果表明,熔体过冷度较大的白口铸铁的共晶结晶是一个复杂的过程,包括晶相γ奥氏体和两种亚稳碳化物Fe3C和Fe7C3的结晶和同时溶解。结晶过程一般为L→L+ Fe7C3 +γ→L++ Fe7C3 +γ+ Fe3C→Fe7C3 +γ+ Fe3C。结果形成两种共晶,一种是具有奥氏体的Fe7C3 +γ(片状),另一种是具有渗碳体基体的莱氏体γ+ Fe3C。科学的新奇。研究了片状Fe7C3 +γ共晶的成核和生长的微观动力学,发现Fe7C3碳化物在正常条件下相对稳定。提出了Fe7C3碳化物在Fe-Fe3C-Fe7C3体系中参与的亚稳相平衡方案。实用价值。提出了一种简单的液相处理技术,以使熔体产生明显的过冷,从而形成一种既有转变奥氏体基体又有碳化物增强相的天然复合材料。
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