Effect of MgO content and CaO/Al2O3 ratio on melting temperature and viscosity of CaF2–CaO–Al2O3–MgO slag for electroslag remelting

IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS
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Abstract

During electroslag remelting (ESR), high MgO contents are typically added to CaF2–CaO–Al2O3 slag to control magnesium content in iron- and nickel-based alloys. The melting temperature and viscosity of ESR slag are pivotal for energy consumption, production efficiency, smooth operation, and ingot quality. However, there is currently a notable scarcity of research on the melting temperature and viscosity of CaF2–CaO–Al2O3–MgO slag with high MgO levels. Thus, the melting temperatures and viscosity of CaF2–CaO–Al2O3–MgO slags with varying MgO contents and CaO/Al2O3 (C/A) ratios were investigated. The results show that as the MgO content increases from 7.83 % to 13.18 %, the final precipitation content of the MgO phase significantly increases, resulting in an increase in the melting temperature from 1306 °C to 1319 °C. With the increase in the C/A ratio from 0.86 to 1.16, the precipitation completion temperatures of the Ca12Al14F2O32 and MgO phases significantly decrease and the MgAl2O4 phase transforms into the CaO phase. Hence, the melting temperature decreases from 1329 °C to 1314 °C. Further increasing the C/A ratio to 1.40, the final precipitation content of the CaO phase increases, resulting in a decrease in the melting temperature from 1314 °C to 1282 °C. Moreover, as the MgO content and C/A ratio increase, the slag viscosity exhibits different change trends within various temperature ranges. This depends on which of the depolymerization of the slag structure and the precipitation and clustering of the MgO phase has a greater effect on the slag viscosity.

氧化镁含量和 CaO/Al2O3 比对电渣重熔用 CaF2-CaO-Al2O3-MgO 熔渣熔化温度和粘度的影响
在电渣重熔(ESR)过程中,通常会在 CaF2-CaO-Al2O3 熔渣中加入高含量的氧化镁,以控制铁基和镍基合金中的镁含量。ESR 熔渣的熔化温度和粘度对能耗、生产效率、平稳运行和铸锭质量至关重要。然而,目前有关高氧化镁含量的 CaF2-CaO-Al2O3-MgO 熔渣的熔化温度和粘度的研究却非常少。因此,我们研究了不同氧化镁含量和 CaO/Al2O3 (C/A) 比的 CaF2-CaO-Al2O3-MgO 熔渣的熔化温度和粘度。结果表明,随着氧化镁含量从 7.83 % 增加到 13.18 %,氧化镁相的最终析出含量显著增加,导致熔化温度从 1306 °C 上升到 1319 °C。随着 C/A 比从 0.86 增加到 1.16,Ca12Al14F2O32 和 MgO 相的沉淀完成温度明显降低,MgAl2O4 相转变为 CaO 相。因此,熔化温度从 1329 °C 降至 1314 °C。将 C/A 比进一步提高到 1.40 时,CaO 相的最终析出含量增加,导致熔化温度从 1314 ℃ 降至 1282 ℃。此外,随着氧化镁含量和 C/A 比的增加,炉渣粘度在不同温度范围内呈现出不同的变化趋势。这取决于熔渣结构的解聚与氧化镁相的沉淀和团聚对熔渣粘度的影响哪个更大。
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来源期刊
Ceramics International
Ceramics International 工程技术-材料科学:硅酸盐
CiteScore
9.40
自引率
15.40%
发文量
4558
审稿时长
25 days
期刊介绍: Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties. Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour. Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.
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