Sürdürülebilir Kalkınma Amaçları

Yazarlar

  • MakaleAçık Erişim2026Scopus SJRQ4
    Solvent Extraction of Copper from Sulfate Solutions Using Acorga OPT5510; [Extracción de cobre de soluciones de sulfato mediante solventes con Acorga OPT5510]

    Karacahan, Mehmet Kayra

    This study used a solvent extraction technique with AcorgaOPT5510 extractant in kerosene to examine the extraction of copper ions from the actual leach solution produced after leaching malachite ore in sulfuric acid solutions. On the Cu/Fe separation factor and the effectiveness of copper extraction, the impacts of significant parameters, including stirring speed, contact duration, extractant concentration, beginning solution pH, and temperature, were examined. The following values were chosen as the optimal ones: 1:1, 1.5, 12%, 20 °C, 10 min, 10 min, and 500 rpm for maximum Cu2+ extraction from the aqueous-phase, aqueous/organic phase ratio, equilibrium pH of the aqueous phase, extractant concentration, temperature, contact time, settling time, and stirring speed. Under these conditions, 94% of the copper in the leach solution was removed, yielding about 40.09 Cu/Fe separation factor. A McCabe-Thiele plot was revealed, and it was shown that a two-step extraction procedure would yield the best results. Furthermore, employing a sulfuric acid concentration of 4 mol·L-1 for 10 minutes, the loaded organic phase was stripped and recovered 91% copper.

    • SDG 12 · Sorumlu Üretim ve Tüketim
  • MakaleYalnız künye2020Scopus SJRQ3
    Kinetic models for the extraction of copper by Acorga M5640 after leaching of malachite ore in perchloric acid solutions and the stripping of copper from loaded organic phase

    Tanaydın, Mehmet Kayra; Demirkıran, Nizamettin

    In the present work, the extraction kinetics of copper using the resulting actual leach solution obtained from the leaching of malachite ore in perchloric acid solutions and the stripping kinetics of copper from the loaded organic phase were examined. The organic phase was prepared by using Acorga M5640 and kerosene. In the extraction process, the effects of the initial pH of aqueous solution, initial concentration of copper, extractant concentration, temperature, and stirring speed on the extraction rate were investigated. In the stripping process, the effects of the concentration of perchloric acid, temperature, stirring speed, and extractant concentration on the stripping rate were examined. It was determined that the extraction rate increased with increasing the initial pH of aqueous solution, stirring speed, extractant concentration and temperature, and with decreasing the initial concentration of copper ions. In the stripping process, it was observed that the stripping rate increased with increasing the concentration of perchloric acid, temperature and stirring speed, and with decreasing the extractant concentration. It was determined that both the solvent extraction and stripping processes could be described by the first order pseudo homogenous reaction model. The activation energy for the extraction and stripping processes was calculated to be 50.04 kJ/mol and 32.42 kJ/mol, respectively.

    AtıfScopus8WoS7OpenAlex10
    ScopusWeb of Scienceİncele
  • MakaleYalnız künye2015Scopus SJRQ1
    Stripping voltammetric analysis of dicofol on graphene-modified glassy carbon electrode

    Koçak, Berna; Er, Engin; Çelikkan, Huseyin

    This study is related to the development of a highly sensitive and selective electrode for the electroanalysis of dicofol (DCF) by the modification of a glassy carbon electrode (GCE) with graphene (GR) nanosheets. GR was characterized by Fourier transform infrared spectroscopy (FTIR), atomic force microscopy (AFM), transmission electron microscopy (TEM), and electrochemical methods. The electrochemical reduction of DCF was observed on both bare GCE and GR-modified GCE (GRE). The electrochemical reaction of DCF on GRE was observed to be an adsorption controlled. Differential pulse stripping voltammetry was chosen in the electrochemical analysis of DCF, and two linear calibration ranges from 5.0 x 10(-8) to 5.0 x 10(-7) M and from 5.0 x 10(-7) to 4.2 x 10(-4) M were obtained with a low detection limit of 1.08 x 10(-7) M (N = 5) under the optimized experimental conditions. The electrode developed was successfully used to monitor dicofol in a series of spiked samples.

    AtıfWoS6OpenAlex9
    Web of Scienceİncele