Abstract

This paper looks at the properties of electric double layer (EDL) found at the surface of activated carbons. The study relied on the electrical conductivity method, which is based on simultaneous use of polarization dependences at direct current and conductometric measurements at alternating current. It was found that the adsorption of gold and silver intensifies in the anode region of carbon surface polarization. Two regions with peak adsorption were identified in the following ranges of potentials: +0.2÷+0.25 and +0.6÷+0.8 V. EDL diffusion helps improve the environment for the adsorption of cyanide complexes of gold and silver by active centres of the adsorbent surface. The authors believe that an increased mass transfer in the first range of potentials can be attributed to a decreased diffusion resistance caused by changed zero charge polarity, while in the second range of potentials it can be attributed to the cyan-ion oxidation reaction and an easier access of the negatively charged cyanide complexes of gold and silver to the positively charged surface of the carbon adsorbent. The polarization dependences by direct current in the anode region tend to monotonously rise, which is indicative of a lower EDL density, an increased conductivity at the adsorbent surface/solution boundary and improved adsorption conditions. Graphs showing a relationship between alternating current and carbon adsorbent potential helped determine maximum conducti vity values, which almost match the peak values of gold and silver adsorption. The authors established that the adsorbent’s potential has a significant effect on the activated carbon adsorption of cyanide complexes of gold and silver. The use of the electrical conductivity method for examining the EDL helps explain certain features typical of the activated carbon adsorption of gold and silver from cyanide solutions.

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