Tool ceramics based on Al2O3–ZrO2–TiCN composite

Powder Metallurgy and Metal Ceramics - Oxide composite Al2O3–ZrO2(Y2O3) powders containing 50 and 70 vol.% Al2O3, are deposited from salt solutions. The surface area of the deposited powders...     

Influence of reaction of Al2O3 and carbonaceous materials in Al2O3–C refractories on aluminum and carbon pick-up of iron

Carbon-containing Al2O3 refractory crucibles and pure Al2O3 refractory crucible were fabricated to study the effect of carbon-containing Al2O3-C refractories on aluminum and carbon pick-up of iron.Refractory crucibles with pure iron powder were placed in a vacuum induction furnace and heated at 1600℃ for regular time under flowing argon atmosphere.The Al and C contents of iron samples were analyzed,and iron samples were also investigated using a field scanning electron microscope equipped with energy-dispersive spectroscope.The results showed that carbon materials did affect the interac?tion of(Al2O3-C)/Fe system,carbothermal reduction in alumina occurred in the reaction system and the extent of reactions depended on the kinds of carbon materials.     

Dissolution behaviour of MgO based refractories in CaO–Al2O3–SiO2 slag

Abstract

Magnesium oxide (MgO) based refractories are widely used in secondary refining processes, and their dissolution into refining slag is the primary cause of their shortened lifespan. The dissolution rate was investigated for sintered MgO and commercial MgO–C and MgO–Cr₂O₃ refractories in a synthesised 50CaO–45Al₂O₃–5SiO₂ liquid (mass-%) slag. The change in slag composition was measured after a refractory sample was placed into the molten slag that was stirred by flowing argon gas at 1773?K. The dissolution rate of the sintered MgO was above those of the MgO–C and MgO–Cr₂O₃ refractories under the same gas flowrate, although the dissolution rate of all samples increased as the gas flowrate was increased from 25 to 75?mL·min^??1. The slag containing 5?mass-% FeO considerably promoted the dissolution of the MgO–C refractory because of the oxidation of carbon by FeO. The dissolution of all the refractories was greatly affected by penetration of the liquid slag, with the mass transfer of MgO in the penetrating slag at lower gas flowrates likely being the rate controlling step. At high gas flowrates, Ar bubbles covered the surface and blocked the contact between the liquid slag and the solid phase, reducing the dissolution rate.     

Study on electrical conductivity of FexO–CaO–SiO2–Al2O3 slags

The composition dependences of electrical conductivity of Fe_xO–CaO–SiO₂–Al₂O₃ slags at different oxygen potentials and temperatures have been studied experimentally in the present work. From the experimental results, the total electrical conductivity and electronic conductivity for all the slags monotonously decrease as increasing CO/CO₂ ratio from about 0 to 1. With the increase of Fe_xO content, the total electrical conductivity and electronic conductivity increase at a fixed CO/CO₂ ratio. It is also found that the ionic conductivity of all the studied slags increases as increasing the CO/CO₂ ratio, which is resulted from the increase of Fe²⁺ ion concentration. In addition, the temperature dependences of ionic, electronic and total conductivity for different compositions obey the Arrhenius law. The electronic transference number exhibits a strong relationship with oxygen potential, but is independent of temperature.     

The Influence of the ZrO2 Solid Solution Amount on the Physicochemical Properties of Al2O3–ZrO2–Y2O3–CeO2 Powders

Powder Metallurgy and Metal Ceramics - Alumina-based nanocrystalline powders with different ZrO2 amounts were produced for the first time by hydrothermal synthesis in an alkaline environment for...     

Effect of Heat Treatment on the Physicochemical Properties of Ultrafine ZrO2–Y2O3–CeO2–Al2O3–CoO Powders

Powder Metallurgy and Metal Ceramics - Variations in the phase composition, specific surface area, and morphology of structural components in the ultrafine powder of composition (wt.%) 70 (90 ZrO2...     

Surface Tensions of Some CaO–MgO–Al2O3–SiO2 Slags

Abstract

The surface tensions of some high basicity alumino-silicates have been determined by the maximum bubble pressure technique. The results, which lie in the range 440–550 mN m^?1, are lower than estimated from predictive models and the reasons for this discrepancy are discussed. It is suggested that the concept of optical basicity can, under appropriate circumstances, be usefully applied to aid the interpretation of surface tension-composition relationships.

Résumé

Les tensions de surface de certains Alumino-Silicates très alcalins ont été déterminées par la technique de pression maximale de bulles. Les résultats qui fluctuent entre 440 et 550 mN m^?1, sont plus bas que les estimés prévus par modélisation et les raisons de ces écarts sont discutés. Il est suggéré que le concept d'alcalinité optique soit appliqué avantageusement dans certain cas, pour aider à l'interprétation des relations tension de surface-composition.     

Effect of Al antioxidant in MgO–C refractory on the formation of Al2O3-rich inclusions in high-carbon steel for saw wire under vacuum conditions

Al₂O₃-rich (>70?wt-%) inclusions generally hard and non-deformable are extremely detrimental for saw wire. In order to explore the source of this type of inclusion and provide solutions, experiments on the interaction between Al-containing MgO–C refractory and high-carbon steel for saw wire was conducted on a laboratorial scale using a cold crucible levitation melting furnace under vacuum conditions. [Al]_S (acid-soluble Al), [C] and [Mg] concentrations in steel, Al₂O₃ concentration in inclusions and microstructure of refractory/steel interface, etc. were analysed to clarify the influence of vacuum pressure, refractory addition amount and interaction time. Based on the experimental results and thermodynamic calculations, a presumable impact mechanism of Al antioxidant in MgO–C refractory on the formation of Al₂O₃-rich inclusions in high-carbon steel for saw wire under vacuum conditions was deduced, which in turn provided a reference for the control of Al₂O₃-rich inclusions in high-carbon steel for saw wire.     

Viscosity of CaO–MgO–Al2O3–SiO2 melts containing SiC particles

The influence of SiC particle on viscosity of CaO–MgO–Al₂O₃–SiO₂ melts was investigated by the rotating-cylinder method. It was found that temperature dependence of viscosity could be described by the Arrhenius law for systems with or without SiC particle addition. The activation energies of liquid–solid mixtures were mainly determined by liquid phase. Temperature had little influence on the relative viscosity (defined as the viscosity ratio of solid–liquid mixture to pure liquid). Viscosity and relative viscosity increased as decreasing rotation speed and increasing volume fraction of SiC solid particle. For the same volume fraction of SiC particle, relative viscosity was affected by the liquid slag compositions. The relative viscosity was smaller when composition of liquid slag had a larger CaO/SiO₂ ratio or MgO/Al₂O₃ ratio. Meanwhile, it was found that the smaller SiC particle will lead to a larger relative viscosity.     

Viscosity of low silica CaO–5MgO–Al2O3–SiO2 slags

Abstract

The viscosity of CaO–5MgO–Al₂O₃–SiO₂ slag with low silica was measured by rotating cylinder method up to 1823 K. Slag compositions were chosen based on five different levels of SiO₂ content between 0 and 11·80%. The MgO content was 5·0%. The mass ratio of CaO/Al₂O₃ was varied from 0·66 to 1·95. It was shown that viscosity decreased with increasing temperature and decreased with increasing the mass ratio of CaO/Al₂O₃, following by an increase with further increasing the mass ratio of CaO/Al₂O₃. The viscosity decreased with the NBO/T ratio increasing, and the trend that flow activation energy changes with the NBO/T ratio of slag was the same as the trend that viscosity changes with the NBO/T ratio. Based on the experimental data as the boundary of the homogenous phase region, the mass triangle model was used to calculate the viscosity of low silica region.     

Kinetics of Na2O evaporation from CaO–Al2O3–SiO2–MgO–TiO2–Na2O slags

The present work is carried out to study the evaporation of Na₂O from CaO–Al₂O₃–SiO₂–TiO₂–MgO–Na₂O slags with high basicity and high alumina in the temperature range of 1500–1560°C. The ratio of evaporation was determined by monitoring the Na₂O content change of the slag melt under isothermal reduction conditions. The results show that the evaporation ratio increases with increasing the temperature. Higher basicity and increasing concentrations of Na₂O, Al₂O₃ are also found to increase the evaporation ratio of Na₂O, while MgO addition only slightly enhances the evaporation ratio. With TiO₂ content increasing, the evaporation ratio first increases and then decreases. The evaporation rate of Na₂O appears to be controlled by chemical reaction at the slag/gas interface in the beginning, followed by a mixed reaction-mass transfer regime, and finally a liquid-phase mass transport step. The apparent activation energy is 134.74?kJ?mol^?1 for the chemical reaction regime and 268.53?kJ?mol^?1 for the liquid-phase mass diffusion step.     

Effect of Al2O3–SiO2–MnO inclusions on precipitation of MnS in Si–Mn-killed 304 stainless steels

Laboratory experiments and thermodynamic calculation were conducted to investigate the precipitation of MnS inclusions in Si–Mn-killed 304 stainless steels with various Al and S concentrations. Three types of MnS-contained inclusions were detected: MnS phase dissolved in the MnO–SiO₂ inclusion, the Al₂O₃-rich core phase surrounded by a MnS out layer, and the individual MnS. In steel with less than 0.001% Al, the liquid SiO₂–MnO-rich inclusions can hardly influence the precipitation of MnS inclusions during the cooling process of 304 stainless steels. With the increase of Al in steel, more solid Al₂O₃-rich inclusions are formed, which can act as nucleation agents for MnS inclusions and dramatically promote the precipitation of MnS inclusions during the cooling process of Si–Mn-killed 304 stainless steels.     

自蔓延高温合成Al2O3＋ZrO2＋Cr复合材料

自蔓延高温合成是制备材料的一种新工艺。通过热力学和显微结构分析研究了Ａｌ－Ｃｒ２Ｏ３－ＺｒＯ２系统，结果表明：在Ａｌ：Ｃｒ２Ｏ３：ＺｒＯ２＝１：２．８：１．４３（ｗｔ）时，可以自蔓延高温合成Ａｌ２Ｏ３－ＺｒＯ２－Ｃｒ复合材料，ＺｒＯ２不与Ａｌ发生反应，产物孔隙度达３５％－４５％。