scholarly journals Influence of Electrolyte Impurities from E-Waste Electrorefining on Copper Extraction Recovery

Metals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1383
Author(s):  
Jovana Djokić ◽  
Dragana Radovanović ◽  
Zlatko Nikolovski ◽  
Zoran Andjić ◽  
Željko Kamberović

In order to reflect possible issues in future sole e-waste processing, an electrolyte of complex chemical composition reflecting system of sole e-waste processing was obtained by following a specially designed pyro-electrometallurgical method. The obtained non-standard electrolyte was further used for the purpose of comprehensive metal interference evaluation on the copper solvent extraction (SX) process. Optimization of the process included a variation of several process parameters, allowing determination of the effect of the most abundant and potentially the most influential impurities (Ni, Sn, Fe, and Zn) and 14 other trace elements. Moreover, comparing three commercial extractants of different active chelating groups, it was determined that branched aldoxime reagent is favorable for Cu extraction from the chemically complex system, as can be expected in future e-waste recycling. The results of this study showed that, under optimal conditions of 20 vol.% extractant concentration, feed pH 1.5, O/A ratio 3, and 10-min phase contact time, 88.1% of one stage Cu extraction was achieved. Co-extraction of the Fe, Zn, Ni, and Sn was under 8%, while Pb and trace elements were negligible. Optimal conditions (H2SO4 180 g/L, O/A = 2, and contact time 5 min) enabled 95.3% Cu stripping and under 6% of the most influential impurities. In addition, an impurity monitoring and distribution methodology enabled a better understanding and design of the process for the more efficient valorization of metals from e-waste.

2019 ◽  
Vol 2 (1) ◽  
pp. 69
Author(s):  
Wardian Antoni ◽  
Saprini Hamdiani ◽  
Siti Raudhatul Kamali

Synthesis of paramagnetic silica from rice husk ash has been carried out as an adsorbent for heavy metal Ag (I). This study tried to synthesis and characterized the thermodynamics and kinetics behaviour of paramagnetic silica from the husk ash as metal adsorbent Ag (I). Determination of optimal conditions for adsorption of metal ions Ag (I) is carried out by varying the pH, concentration, and contact time of the adsorbent. The results showed that the optimum pH was at pH 3, optimal concentration Ag(I) of 350 ppm and optimal contact time of 90 minutes. At optimal conditions, paramagnetic silica adsorption capacity for metal ion Ag (I) is 323.62 mg/g. The isotherm model that is suitable for paramagnetic silica is the Freundlich isotherm model. The kinetic model that is suitable for paramagnetic silica is the Pseudo Order 2 kinetic model.


2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.


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