Complexing agent study for environmentally friendly silver electrodeposition(ii): electrochemical behavior of silver complex

RSC Advances ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 7348-7355 ◽  
Author(s):  
Anmin Liu ◽  
Xuefeng Ren ◽  
Jie Zhang ◽  
Deyu Li ◽  
Maozhong An

Silver deposition and electrochemical behaviors of silver complex in the environmentally friendly silver plating bath were studied.

RSC Advances ◽  
2021 ◽  
Vol 11 (13) ◽  
pp. 7225-7225
Author(s):  
Anmin Liu ◽  
Xuefeng Ren ◽  
Bo Wang ◽  
Jie Zhang ◽  
Peixia Yang ◽  
...  

Correction for ‘Complexing agent study via computational chemistry for environmentally friendly silver electrodeposition and the application of a silver deposit’ by Anmin Liu et al., RSC Adv., 2014, 4, 40930–40940, DOI: 10.1039/C4RA05869K.


RSC Advances ◽  
2014 ◽  
Vol 4 (77) ◽  
pp. 40930-40940 ◽  
Author(s):  
Anmin Liu ◽  
Xuefeng Ren ◽  
Bo Wang ◽  
Jie Zhang ◽  
Peixia Yang ◽  
...  

Predicting the complexing agents used for a new environmentally friendly silver electroplating bath by computational chemistry.


Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 924 ◽  
Author(s):  
Francisco Gálvez ◽  
Marta Cabello ◽  
Pedro Lavela ◽  
Gregorio F. Ortiz ◽  
José L. Tirado

Sodium and magnesium batteries with intercalation electrodes are currently alternatives of great interest to lithium in stationary applications, such as distribution networks or renewable energies. Hydrated laminar oxides such as birnessites are an attractive cathode material for these batteries. Sodium and potassium birnessite samples have been synthesized by thermal and hydrothermal oxidation methods. Hybrid electrochemical cells have been built using potassium birnessite in aqueous sodium electrolyte, when starting in discharge and with a capacity slightly higher than 70 mA h g−1. Hydrothermal synthesis generally shows slightly poorer electrochemical behavior than their thermal counterparts in both sodium and potassium batteries. The study on hybrid electrolytes has resulted in the successful galvanostatic cycling of both sodium birnessite and potassium birnessite in aqueous magnesium electrolyte, with maximum capacities of 85 and 50 mA h g−1, respectively.


1990 ◽  
Vol 5 (8) ◽  
pp. 1612-1615 ◽  
Author(s):  
J. M. Rosamilia ◽  
B. Miller

A nonaqueous plating bath for silver deposition on the Ba2YCu3O7 superconductor has been modified with thiourea to give enhanced coverage of the metal film at low thicknesses. For both porous and high density ceramic substrates, SEM and optical microscopy show nucleation of silver deposits is increased by the additive. The resulting silver-superconductor contact resistances are comparable to those achieved without additives. Adhesion of the deposits and ease of mechanical handling are improved with thiourea. The combination of highly reactive oxidized substrate, nonaqueous solvent, and strongly surface active agent forms a novel extension for electrodeposition science.


2022 ◽  
Vol 3 (33) ◽  
pp. 05-20
Author(s):  
Mahmoud A. Rabah ◽  
◽  
Nabil Nassif Girgis ◽  

This study shows a silver electrodeposition model (EDM) on a graphite ‎substrate. The electrolyte was a 0.01 M solution of pure silver and chromium nitrate using an ‎electrolyzing cell. EDC with current density up to 20 mA/cm2 and 15 mV and pulse current were studied. Results revealed that silver deposited at a ‎rate of 0.515 mg/cm2/min with 12 mA /cm2 that decreases to 0.21 and 0.16 mg/cm2.min ‎with the decrease of current density to 6 and 5 mA/cm2 respectively. The model postulates that ‎silver ions (a) were first hydrated before diffusing (b) from the solution bulk to ‎the cathode vicinity, the next step (c) involved the chemical adsorption of these ions on certain ‎accessible sites of the graphite substrate (anode), the discharged entities (d) adhere to the graphite ‎surface by Van der Vales force. Silver ions are deposited because the ‎discharge potential of silver is low (0.38 mV) as compared to other metal ions like chromium (0.82 mV). Pulse ‎current controls silver deposition due to flexibility in controlling steps (a) - (c) of the ‎deposition mechanisms.


2020 ◽  
Vol 67 (6) ◽  
pp. 593-603
Author(s):  
Refaie Omar ◽  
Elsayed Oraby ◽  
Yasser Abdelrhman ◽  
Mohammed Aboraia

Purpose The ability to produce a uniform composition, high corrosion resistance with a hard coating layer during the electroless coating techniques are mainly based on the plating bath composition. The complexing agent is one of the most important components that control the coating layer properties. This paper aims to investigate the effect of the glycine as a complex agent on the surface and corrosion properties of Ni-P and Ni-P/Al2O3 electroless coating. Design/methodology/approach In this study, the effect of glycine as a complexing agent on the final surface and corrosion properties of the Ni-P and Ni-P/Al2O3 coatings has been investigated. The surface morphology and composition of the coated samples were investigated by scanning electron microscope (SEM) imaging and energy dispersive x-ray spectroscopy (EDS) analysis. Linear polarization scan and electrochemical impedance spectroscopy techniques were used to investigate the corrosion properties of the coating layer. Findings The results clarify that, glycine has a remarkable effect on the porosity content of Ni-P and Ni-P/Al2O3. It was found that increasing of glycine concentration results in higher porosity content in the coating layers. Also, the porosity in the coating layers minimizes the protectability of the coating against corrosion. The results also show that adding nano-alumina (Al2O3) to the coating path has improved the corrosion properties by decreasing the porosity in the coating layer. The scanning electron microscope (SEM) images showed that the concentration of glycine affects the content and distribution of alumina nanoparticles embedded in the coating layer. Also, it was observed that using a high concentration of glycine (0.4 M glycine), the alumina tends to agglomerate and the final alumina content in the coating was decreased. Originality/value The present study reveals that the quality of the final coating plays a major role in the corrosion performance of the steel substrate. The coating quality can by improve remarkably by optimization of the complexing agent used in the plating bath, to minimize the porosity involve in the coating layer.


2013 ◽  
Vol 2013 (1) ◽  
pp. 000667-000671
Author(s):  
Norbert Schroeder ◽  
Fred Richter ◽  
Juerg Stahl ◽  
Arnold Cziurlok

A new tool has been invented that enables a fast and efficient execution of design of experiments (DOE) for the characterization of electroplating chemistries. This new procedure uses a commercially available analysis system (tool). It is fully automated and systematically handles up to four different additives in conjunction with basic electrolytes to evaluate the impact of these on the electrochemical behavior of the plating bath.


2015 ◽  
Vol 162 (9) ◽  
pp. D412-D422 ◽  
Author(s):  
Zhongbao Feng ◽  
Qingyang Li ◽  
Jinqiu Zhang ◽  
Peixia Yang ◽  
Maozhong An

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