scholarly journals Features of the discharge of zinc in the background solution of sodium sulphate under stirring conditions

Author(s):  
Alexander V. Kolesnikov ◽  
Egor I. Ageenko

The production technology of hydrometallurgical zinc uses various surfactants to thicken pulps, stabilise the electrolysis process, and obtain high-quality cathode deposits. Numerous researches were conducted to study the cathodic and anodic processes in a wide range of the composition of aqueous solutions using various solid electrodes in the absence of intense stirring of the electrolyte and with a high contribution of the migration component of the discharge of metals. This approach to the study of the surfactants’ influence rarely provided a high degree of statistical reliability in observing the effect of differently charged surfactants on electrode processes, which is of great importance in the hydrometallurgical production of zinc. In this work, the task was to practically eliminate the contribution of the migration component due to the followingfactors: conducting electrolysis in a background solution of sodium sulphate, organising electrolyte stirring, performing calculations of current densities at the beginning of electrolysis, and establishing polarisation curves at an increased potential sweep rate from 20 to 100 mV/s. This approach provided a greater degree of statistical reliability in presenting the mechanism of the effect of additions of cationic and anionic surfactants during the stage of zinc discharge on a solid electrode, which was the purpose of the article.Electrolysis was conducted in the potential range from -1050 to -1250 mV relative to the silver chloride electrode (AgCl/Ag) in the presence of a background sodium sulphate solution (0.5 M of Na2SO4 solution) containing 0.005, 0.0125, and 0.025 M ZnSO4 with the introduction of high-molecular surfactants: cationic and anionic coagulants (flocculants) and foaming agents (lignosulphonate – LSTP).During the electrolysis in a background solution of sodium sulphate with stirring, it was found that the process of discharge of zinc ions on a solid electrode occurs in a mixed-kinetic mode. It was shown that positively charged additives, such as lignosulphonate and cationic coagulant (flocculant) Besfloc K6645, have a negative effect on the dynamics of zinc cation discharge, while negatively charged Besfloc K4034 has practically no effect. The approach proposed in this work allows evaluating the influence of additions of cationic and anionic surfactants on the stage of zinc discharge on a solid electrode, which was the practical and scientific value of this work

Author(s):  
A.V. Kolesnikov

We investigated the cathodic and anodic processes in solutions of zinc sulfate in the presence of a surfactant and the background solution of sodium sulfate over a wide potential range. It was shown that anionic surfactants increase the anode current and the cation ones decrease. An explanation for the increase in the magnitude of the anode current in presence of anionic surfactants and reduction in the presence of cation-active surfactant was done. Experimental data and thermodynamic calculations has shown that the reason for the lack of influence of surfactants on the magnitude of the cathode current for the background electrolyte solution of sodium sulfate is probably associated with the processes of sulfate reduction.


Author(s):  
E. Naranjo

Equilibrium vesicles, those which are the stable form of aggregation and form spontaneously on mixing surfactant with water, have never been demonstrated in single component bilayers and only rarely in lipid or surfactant mixtures. Designing a simple and general method for producing spontaneous and stable vesicles depends on a better understanding of the thermodynamics of aggregation, the interplay of intermolecular forces in surfactants, and an efficient way of doing structural characterization in dynamic systems.


2013 ◽  
Vol 408 ◽  
pp. 164-172 ◽  
Author(s):  
Kun Ma ◽  
Leyu Cui ◽  
Yezi Dong ◽  
Tianlong Wang ◽  
Chang Da ◽  
...  

Langmuir ◽  
2004 ◽  
Vol 20 (6) ◽  
pp. 2117-2122 ◽  
Author(s):  
Koji Tsuchiya ◽  
Hisanori Nakanishi ◽  
Hideki Sakai ◽  
Masahiko Abe

1982 ◽  
Vol 28 (9) ◽  
pp. 1968-1972 ◽  
Author(s):  
K R Wehmeyer ◽  
H B Halsall ◽  
W R Heineman

Abstract The binding of electroactively labeled estriol with estrogen-specific antibody and its subsequent displacement by unlabeled estriol have been monitored by differential pulse polarography. Estriol was found to be electro-inactive in the potential range -200 mV to -1000 mV vs a silver/silver chloride electrode. Estriol labeled in the 2 and 4 position with nitro groups was electroactive, giving two reduction waves at -422 mV and -481 mV vs a silver/silver chloride electrode. The peak current was linear with concentration over the range 60 micrograms/L to 3.7 mg/L. The addition of aliquots of estrogen-specific antibody reduced the peak current proportionately, indicating the binding of ligand to specific antibody. Subsequent addition of unlabeled estriol produced incremental increases in peak reduction current, indicating competitive and reversible binding of the two ligands for the antibody. Separation of bound from free labeled hapten was not necessary because reduction of the antibody-bound labeled estriol is attenuated at the electrode.


2010 ◽  
Vol 114 (31) ◽  
pp. 13385-13389 ◽  
Author(s):  
C. Lo ◽  
J. S. Zhang ◽  
A. Couzis ◽  
P. Somasundaran ◽  
J. W. Lee

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