Electrochemical reduction processes and extraction of titanium with different valence states in molten CaO-CaF2 slags

IF 5.8 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Journal of Alloys and Compounds Pub Date : 2024-06-27 DOI:10.1016/j.jallcom.2024.175379
Liqi Zhang, Xu Zhang, Bowen Huang, Yusheng Yang, Zengwu Zhao
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Abstract

Titanium is an excellent structural and functional material. At present, the production of titanium has long process cycle, high energy consumption, serious pollution and other characteristics, so the development of low-cost titanium production methods has extremely far-reaching significance. In this work, the electrochemical reduction process of Ti(IV) and Ti(II) in the CaF-CaO melt were investigated by cyclic voltammetry and square wave voltammetry measurements at 1740 K, respectively. In the CaF-CaO-5 wt% TiO melt, Ti(IV) ions were reduced to Ti by one step. One measure was taken to lower the valence state of Ti ions: Ti(IV) ions in the melt was changed to Ti(II) by adding Ti. Ti(IV) ions were reduced in two steps: in the CaF-CaO-5 wt% TiO-Ti melt, Ti(IV) → Ti(II) and Ti(II) → Ti, respectively, and in the CaF-CaO-5 wt% TiO, the Ti(II) ions were reduced in a single step: Ti(II) → Ti. It was found that both migration and mass transfer affected the reduction processes. In contrast to the Ti(IV) reduction to Ti process, the Ti(II) reduction to Ti process showed a higher diffusion rate. Electrolytes and electrodes were analyzed after titanium electrodeposition by XRD. It was found that there were no metal titanium was detected in the electrolyte placed close to the cathode after electrodeposition. It believed that the formed metallic Ti reacted with dissolved O in the melt to form TiO. The reduction process of Ti(IV) on the iron electrode was investigated, the metal Ti was reduced by alloying process, the oxidation of Ti was hindered, there was a dense structure layer of CaTiO outside the reduced metal Ti that prevented the ions transfer and affected the Ti(IV) ions migration process, which might be the main factor that the Ti(IV) reduction process was controlled by migration. The lower valence state of Ti in the melt promoted the formation of CaTiO, which increased the ion migration rate and decreased the mass transfer rate. It was suggested that titanium or titanium alloys may be prepared by reducing the valence of Ti(IV) in minerals and altering the melt composition. It is feasible to prepare titanium and titanium alloys by MOE short process using ore as raw material.

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熔融 CaO-CaF2 熔渣中的电化学还原过程和不同价态钛的提取
钛是一种优良的结构材料和功能材料。目前,钛的生产具有工艺周期长、能耗高、污染严重等特点,因此开发低成本的钛生产方法具有极其深远的意义。本研究采用循环伏安法和方波伏安法,在 1740 K 下分别研究了 Ti(IV) 和 Ti(II) 在 CaF-CaO 熔体中的电化学还原过程。在 CaF-CaO-5 wt% TiO 熔体中,Ti(IV) 离子一步还原成 Ti。其中一个措施是降低 Ti 离子的价态:通过添加 Ti,将熔体中的 Ti(IV) 离子转变为 Ti(II)。Ti(IV) 离子分两步被还原:在 CaF-CaO-5 wt% TiO-Ti 熔体中,Ti(IV) → Ti(II) 和 Ti(II) → Ti 分别被还原;而在 CaF-CaO-5 wt% TiO 中,Ti(II) 离子被一步还原:Ti(II) → Ti。研究发现,迁移和传质都会影响还原过程。与 Ti(IV) 还原成 Ti 的过程相比,Ti(II) 还原成 Ti 的过程显示出更高的扩散率。通过 XRD 分析了钛电沉积后的电解质和电极。结果发现,在电沉积后靠近阴极的电解液中没有检测到金属钛。这表明形成的金属钛与熔体中溶解的 O 反应生成了 TiO。研究了 Ti(IV)在铁电极上的还原过程,金属 Ti 在合金化过程中被还原,Ti 的氧化受阻,在被还原的金属 Ti 外有一层致密的 CaTiO 结构层,阻止了离子的转移,影响了 Ti(IV)离子的迁移过程,这可能是 Ti(IV)还原过程受迁移控制的主要因素。熔体中钛的价态较低,促进了 CaTiO 的形成,从而增加了离子迁移率,降低了传质速率。研究表明,可以通过降低矿物中 Ti(IV)的价态并改变熔体成分来制备钛或钛合金。以矿石为原料,采用 MOE 短流程制备钛和钛合金是可行的。
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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