Copper-decorated CNTs as a possible electrode material in supercapacitors

Copper is probably one of the most important metal used in the broad range of electronic applications. It has been developed for many decades, and so it is very hard to make any further advances in its electrical and thermal performance by simply changing the manufacture to even more oxygen-free conditions. Carbon nanotubes (CNTs) due to their excellent electrical, thermal and mechanical properties seem like an ideal component to produce Cu-CNT composites of superior electrochemical performance. In this report we present whether Cu-CNT contact has a beneficial influence for manufacturing of a new type of carbon-based supercapacitor with embedded copper particles. The prepared electrode material was examined in symmetric cell configuration. The specific capacity and cyclability of composite were compared to parent CNT and oxidized CNT

Active Carbon Modified by Rhenium Species as a Perspective Supercapacitor Electrode

We have reported the synthesis of a new kind of composite combining a rhenium precursor and active carbon. Similarly to other refractory metals, rhenium exhibits several oxidation states that makes it an ideal candidate for redox-type energy storage materials. A simple impregnation of pretreated active carbon with ammonium perrhenate allowed to produce an electrode material with an enhanced specific capacitance. There was not any observed detrimental effect of metal species on the cycle life of the electrode. A small increase in charge transfer resistance was counter-balanced by the improved impedance in the whole examined range

Technology to Produce High-Purity Anhydrous Rubidium Perrhenate on an Industrial Scale

Technology used to produce high purity anhydrous rubidium perrhenate on an industrial scale from high purity perrhenic acid and rubidium nitrate by the ion-exchange method is described in this paper. This material is dedicated to catalyst preparation, therefore, strict purity requirements have to be fulfilled. These are satisfied by combining rubidium ion sorption on an ion exchange column and the subsequent elution of the high purity perrhenic acid solution, followed by crystallization, evaporation, purification, and drying. In the current study, rubidium and rhenium contents were found to be 22.5 wt.% and 55.4 wt.%, respectively, while contaminations were as follows: <2 ppm As, <2 ppm Bi, <5 ppm Ca, <5 ppm Cu, <3 ppm Fe, <10 ppm K, <3 ppm Mg, <5 ppm Mo, <2 ppm Na, <5 ppm Pb, and <3 ppm Zn

Purification of Industrial Copper Electrolyte from Bismuth Impurity

This work focused on purifying copper electrolytes from a bismuth impurity on a laboratory scale. The electrolyte came from Polish copper electrorefineries with the content of main components, g/dm3: 49.6 Cu, 160 H2SO4. The electrolyte was enriched in bismuth by Bi2O3 addition. Purification of bismuth contamination was carried out using selected agents with adsorbing effects, such as barium hydroxide octahydrate, strontium carbonate, barium carbonate, barium and lead sulfates. The trials were performed until achieving the Bi level—below 0.1 g/dm3. During the experiments, it was noticed that electrolyte purification degree depends on initial Bi concentration in electrolyte, time and temperature, as well as on the type and amount of the bismuth-lowering agent. The most satisfactory results of Bi impurity removal were with additions of barium hydroxide octahydrate, strontium carbonate and barium carbonate to electrolyte at 60 °C for 1 h. These parameters revealed the highest electrolyte purification degree. Bismuth is not removed effectively from electrolytes by barium sulfate or lead sulfate addition. The efficiency of the purification process is much higher when the agents are added to the solution in the form of carbonates or hydroxides. Extending the electrolyte purification process time may cause dissolution of bismuth from the resulting precipitate and increase of bismuth concentration in electrolytes