电解锰生产中提高阳极液酸度的措施

从阴极液pH值的控制,阴、阳极隔离条件,电解液补给量,外部水的带入等几方面,分析了影响电解阳极液含酸量的原因,并提出了应采取的相应措施。

Effect of impurities in recycling water on Pb-Ag anode passivation in zinc electrowinning process

Effect of impurities in recycling water on Pb-Ag anode passivation in zinc electrowinning process was investigated by linear scan voltammetry.Results show that passivation process would be affected in the presence of Cl^-and F-in recycling water.It was highly advantageous to take H2SO4 concentration as 180g/L,Mn^2＋ concentration as 3-5 g/L and F-less than 42mg/L.However,passivation process would not be affected when Cl^-concentration was less than 13mg/L without any other ions,or when mass ratio of Mn^2＋ to Cl^-existing in electrolyte was 8,where Cl^-concentration could reach up to 625mg/L.

Electrosynthesis of α-phenyllevulinic acid from benzalacetone and carbon dioxide

Electrocarboxylation ofbenzalacetone was studied in the presence of an atmospheric pressure of CO2 The only carboxylic product obtained was α-phenyl levulinic acid in a one-compartment electrochemical cell equipped with a Mg sacrificial anode at the controlled potential conditions. Influences of the solvents, the electrolytes, the cathode materials, the electrolysis potentials, the concentrations of substrate and the temperatures were studied to improve the yield. The maximal yield is 69% in MeCN-0.1 mol/L TEABF4 on Stainless steel-Mg under a controlled potential of-1.6 V vs.Ag/AgI until 2 F/mol of charge had passed through the cell at 0 ℃.

Influence of oxidation heat on hard anodic film of aluminum alloy

The special experimental device and sulfuric acid electrolyte were adopted to study the influence of anodic oxidation heat on hard anodic film for 2024 aluminum alloy. Compared with the oxidation heat transferred to the electrolyte through anodic film, the heat transferred to the coolant through aluminum substrate is more beneficial to the growth of anodic film. The film forming speed, film thickness, density and hardness are significantly increased as the degree of undercooling of the coolant increases. The degree of undercooling of the coolant, which is necessary for the growth of anodic film, is related to the degree of undercooling of the electrolyte, thickness of aluminum substrate, thickness of anodic film, natural parameters of bubble covering and current density. The microstructure and performance of the oxidation film could be controlled by the temperature of the coolant.

Effect of coke properties and its blending recipe on performances of carbon anode for aluminium electrolysis

The properties and blending recipe of petroleum cokes used to make high quality carbon anodes for aluminium electrolysis were studied. Three kinds of green cokes were selected for bench scale study to illustrate the effects of cokes properties and its blending recipe on anode performances. The results show that impurities derived mainly fi＇om cokes remarkably affect the CO2 reactivity and air reactivity of carbon anodes. Ca, Na and V can increase CO2 reactivity of calcined cokes but S has the contrary effect, and the cokes of high V level generally present high air reactivity. The anodes with good quality can be made by properly selecting and scientifically blending of cokes, some poor quality cokes can also be used to produce high quality anodes with a reasonable blending recipe. Na contaminated anodes have high CO2 reactivity and air reactivity, so the recycled anode butts should be well cleaned to reduce Na content before being introduced into anode production, which is especially important to the low S cokes.

Effect of Anodization Parameters on Morphologies of TiO2 Nanotube Arrays and Their Surface Properties

This work presents the potentiostatic anodization study of titania nanotube array films fabricated in fluoride-based organic electrolytes including DEG （diethylene glycol） and EG （ethylene glycol）. The work focuses on the effect of important anodization parameters such as applied voltage, anodization time, and electrolyte type on nanotube morphologies and corresponding surface properties. Depending upon unique nanotube formation structures obtained from each anodizing electrolyte, wettability of the nanotube array layer has been determined by means of the contact angle measurement. The EG nanotube array films with close-packing cell orientation are found to show hydrophilic behavior. While the well separated DEG nanotube array films are found to exhibit hydrophobic behavior, with the characteristics of more discrete, wider cell separation obtained through manipulating the electrolyte conditions and the fabrication techniques offering considerable prospects for developing the superhydrophobic sample surface. Such formation structures observed for the DEG fabricated nanotube is believed to play a prominent role in determining the surface wettability of the anodized nanotube array film. The achieved result in this work is anticipated to pave the way to other relevant applications, where interfacial properties are critically concerned.

Effect of cations in ionic liquids on the electrochemical performance of lithium-sulfur batteries

Lithium-sulfur(Li-S) battery is a promising choice for the next generation of high-energy rechargeable batteries, but its application is impeded by the high dissolution of the polysulfides in commonly used organic electrolyte. Room temperature ionic liquids(RTILs) have been considered as appealing candidates for the electrolytes in Li-S batteries. We investigated the effect of cations in RTILs on the electrochemical performance for Li-S batteries. Ex situ investigation of lithium anode for Li-S batteries indicates that during the discharge/charge process the RTIL with N-methyl-N-propylpyrrolidine cations(P13) can effectively suppress the dissolution of the polysulfides, whereas the RTIL with 1-methyl-3-propyl imidazolium cation(PMIM) barely alleviates the shuttling problem. With 0.5 mol L-1 LiTFSI/P13 TFSI as the electrolyte of Li-S battery, the ketjen black/ sulfur cathode material exhibits high capacity and remarkable cycling stability, which promise the application of the P13-based RTILs in Li-S batteries.