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氧化镁稳定的氧化锆固体电解质辅助下在1723K温度对SiO-CaO-MgO-AlO熔渣中铁离子的电化学研究

Magnesia-stabilised zirconia solid electrolyte assisted electrochemical investigation of iron ions in a SiO-CaO-MgO-AlO molten slag at 1723 K.

作者信息

Gao Yunming, Yang Chuanghuang, Zhang Canlei, Qin Qingwei, Chen George Z

机构信息

The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, China.

出版信息

Phys Chem Chem Phys. 2017 Jun 21;19(24):15876-15890. doi: 10.1039/c7cp01945a.

Abstract

Production of metallic iron through molten oxide electrolysis using inert electrodes is an alternative route for fast ironmaking without CO emissions. The fact that many inorganic oxides melt at ultrahigh temperatures (>1500 K) challenges conventional electro-analytical techniques used in aqueous, organic and molten salt electrolytes. However, in order to design a feasible and effective electrolytic process, it is necessary to best understand the electrochemical properties of iron ions in molten oxide electrolytes. In this work, a magnesia-stabilised zirconia (MSZ) tube with a closed end was used to construct an integrated three-electrode cell with a "MSZ|Pt|O (air)" assembly functioning as the solid electrolyte, the reference electrode and also the counter electrode. Electrochemical reduction of iron ions was systematically investigated on an iridium (Ir) wire working electrode in a SiO-CaO-MgO-AlO molten slag at 1723 K by cyclic voltammetry (CV), square wave voltammetry (SWV), chronopotentiometry (CP) and potentiostatic electrolysis (PE). The results show that the electroreduction of the Fe ion to Fe on the Ir electrode in the molten slag follows a single two-electron transfer step, and the rate of the process is diffusion controlled. The peak current on the obtained CVs is proportional to the concentration of the Fe ion in the molten slag and the square root of scan rate. The diffusion coefficient of Fe ions in the molten slag containing 5 wt% FeO at 1723 K was derived to be (3.43 ± 0.06) × 10 cm s from CP analysis. However, a couple of subsequent processes, i.e. alloy formation on the Ir electrode surface and interdiffusion, were found to affect the kinetics of iron deposition. An ECC mechanism is proposed to account for the CV observations. The findings from this work confirm that zirconia-based solid electrolytes can play an important role in electrochemical fundamental research in high temperature molten slag electrolytes.

摘要

使用惰性电极通过熔融氧化物电解生产金属铁是一种无CO排放的快速炼铁替代途径。许多无机氧化物在超高温(>1500 K)下熔化这一事实对用于水性、有机和熔盐电解质的传统电分析技术提出了挑战。然而,为了设计可行且有效的电解工艺,有必要深入了解熔融氧化物电解质中铁离子的电化学性质。在这项工作中,使用一端封闭的氧化镁稳定氧化锆(MSZ)管构建了一个集成三电极电池,其中“MSZ|Pt|O(空气)”组件用作固体电解质、参比电极和对电极。通过循环伏安法(CV)、方波伏安法(SWV)、计时电位法(CP)和恒电位电解法(PE),在1723 K的SiO-CaO-MgO-AlO熔渣中,在铱(Ir)丝工作电极上系统地研究了铁离子的电化学还原。结果表明,在熔渣中Ir电极上Fe离子电还原为Fe遵循单一的双电子转移步骤,并且该过程的速率受扩散控制。所得CV上的峰值电流与熔渣中Fe离子的浓度和扫描速率的平方根成正比。通过CP分析得出,在1723 K含5 wt% FeO的熔渣中Fe离子的扩散系数为(3.43 ± 0.06) × 10 cm² s⁻¹。然而,发现后续的一些过程,即在Ir电极表面形成合金和相互扩散,会影响铁沉积的动力学。提出了一种ECC机制来解释CV观测结果。这项工作的发现证实了基于氧化锆的固体电解质在高温熔渣电解质的电化学基础研究中可以发挥重要作用。

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