Preparation of Co-Ni-Ce/TiC alloy coatings by double-pulse under a sulfamic acid system and a process mechanism study.

To enhance the protective ability of copper crystallizers and extend their service life, this study explores the use of double pulse co-deposition under a sulfamic acid system to create protective coatings such as Co-Ni. The hardness test and friction wear analysis compare Co-Ni, Co-Ni-Ce, and Co-Ni-Ce/TiC coatings, revealing that the Co-Ni-Ce/TiC coating exhibits the most outstanding protective performance. SEM and XRD techniques are employed to characterize the three protective coatings, demonstrating that the incorporation of rare-earth cerium and nanoparticles improves the coating morphology and modifies their crystalline phase structure. Furthermore, cyclic voltammetry tests on the plating solutions of the three protective coatings indicate that the addition of Ce3+ and nanoparticles influences the deposition potentials. The deposition of Co2+ and Ni2+ follows a two-step, two-electron process, while the deposition of Ce3+ follows a one-step, three-electron process. It is observed that the deposition of all three ions is irreversible. To gain further insights into the nucleation mechanism of Ce3+, a chronoamperometry test is conducted, revealing that the nucleation of Ce3+ is a transient process controlled by diffusion.

Repair of soft magnetic properties of wasted silicon steel and Co7Fe3 alloy deposition mechanism.

In order to repair the soft magnetic properties of wasted silicon steel, a theoretical process of co-depositing Co-Fe soft magnetic alloy on the surface of wasted silicon steel is proposed. The results show that the co-deposited Co-Fe alloy coatings can serve to repair the soft magnetic properties of wasted silicon as detected by the vibrating sample magnetometer, and the alloy coatings with Co7Fe3 as the main phase structure can provide surface protection for silicon steel. Subsequently, the mechanism of co-deposited Co-Fe alloys was investigated, and it was concluded that Co2+ and Fe2+ undergo a one-step two-electron co-deposition reaction, as studied using cyclic voltammetry. The chronoamperometric analysis and its fitting results indicated that the deposition of Co2+ and Fe2+ was a diffusion-controlled transient nucleation process, and the AC impedance indicated that higher voltages were favorable for the deposition of Co-Fe alloys but were accompanied by hydrogen precipitation reactions.

Electrochemical Mechanism of the Preparation of High-Purity Indium by Electrodeposition.

Indium is a crucial material and is widely used in high-tech industries, and electrodeposition is an efficient method to recover rare metal resources. In this work, the electrochemical behavior of In3+ was investigated by using different electrochemical methods in electrolytes containing sodium and indium sulfate. Cyclic voltammetry (CV), chronoamperometry (CA), and alternating current impedance (EIS) techniques were used to investigate the reduction reaction of In3+ and the electrocrystallization mechanism of indium in the indium sulfate system. The cyclic voltammetry results showed that the electrodeposition process is irreversible. The average charge transfer coefficient a of In3+ was calculated to be 0.116 from the relationship between the cathodic peak potential and the half-peak potential, and the H+ discharge occurred at a higher negative potential of In3+. The nucleation mechanism of indium electrodeposition was analyzed by chronoamperometry. The mechanism of indium at potential steps of -0.3 to -0.6 V was close to diffusion-controlled instantaneous nucleation with a diffusion coefficient of 7.31 × 10-9 cm2 s-1. The EIS results demonstrated that the reduction process of In3+ is subject to a diffusion-controlled step when pH = 2.5 and the applied potential was -0.5 V. SEM and XRD techniques indicated that the cathodic products deposited on the titanium electrode have excellent cleanliness and purity.