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Direct electrochemical reduction of titanium-bearing compounds to titanium-silicon alloys in molten calcium chloride

机译:在熔融氯化钙中将含钛化合物直接电化学还原为钛硅合金

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Titanium-silicon alloys have been electrochemically extracted from the multi-component titanium compounds in molten calcium chloride electrolyte. Sintered pressed pellets of titanium-bearing compounds served as the cathode, and the electrochemical experiments were systematically carried out at 900 °C, 3.1 V and 1000 °C, 3.8 V using a graphite-based anode and an improved inert-oxygen-ion-conducting membrane-based anode, respectively. The mineral composition and morphology of the products were examined. The current feature and the reaction process are discussed, and the mechanisms involved in the electrochemical reduction of titanium-bearing compounds to titanium-silicon alloys are proposed. Comparison between the graphite- and membrane-based anode systems are also carried out, and the results show that the improved membrane-based anode electrolysis system exhibits higher current efficiency and reduction rate than the graphite-based anode electrolysis system. Interestingly, the other metallic impurities such as Ca, Mg and Al contained in the starting titanium compounds have been partly even completely removed during electro-deoxidation, and the removal mechanism is discussed in the paper too. The experimental results show that titanium-silicon alloy (Ti5Si3) can be directly extracted from titanium-bearing compounds using electro-deoxidation technology in molten CaCl2. Electrolysis of ~1.5 g titanium compounds using the membrane-based anode system can be finished within 6 h, and the current efficiency reaches approximately 50%.
机译:从熔融氯化钙电解质中的多组分钛化合物中电化学提取了钛硅合金。含钛化合物的烧结压制小球用作阴极,并使用石墨基阳极和改进的惰性氧离子-电极在900°C,3.1 V和1000°C,3.8 V下系统地进行了电化学实验。分别传导基于膜的阳极。检查了产品的矿物组成和形态。讨论了电流特征和反应过程,并提出了将含钛化合物电化学还原成钛硅合金的机理。还进行了石墨基和膜基阳极系统的比较,结果表明,改进的膜基阳极电解系统比石墨基阳极电解系统具有更高的电流效率和还原率。有趣的是,起始钛化合物中所含的其他金属杂质(如Ca,Mg和Al)在电脱氧过程中已被部分甚至完全去除,并且在本文中也讨论了去除机理。实验结果表明,在熔融的CaCl2中,可以采用电脱氧技术从含钛化合物中直接提取钛硅合金(Ti5Si3)。使用基于膜的阳极系统可完成约1.5 g钛化合物的电解,并且电流效率达到约50%。

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