WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Rare Earth Elements in the Global Economy: Usage, Recovery, and the Quest for Supply Security – A Review(Springer Heidelberg, 2026) Top, Soner; Ayten, Asim Mustafa; Altiner, Mahmut; Demir, Idris; Kursunoglu, SaitOften described as the vitamins of modern industry, rare earth elements (REEs) are indispensable for the deployment of low-carbon and clean energy technologies. However, ensuring a secure and sustainable REE supply remains a major challenge due to the strong interdependence between application-driven demand, extraction and processing technologies, and the geopolitical concentration of resources. This review adopts an integrated analytical framework in which these three dimensions are treated as interconnected components shaping the resilience of global REE supply chains. First, the major application sectors of REEs are examined to clarify how emerging energy and advanced manufacturing technologies drive demand for specific elements and amplify their strategic importance. Second, extraction and processing technologies are reviewed in relation to both primary and secondary resources, highlighting how technological maturity, process selection, and material characteristics constrain or enable supply expansion. Finally, geopolitical and strategic aspects of the REE supply chain are analyzed to demonstrate how resource concentration, policy instruments, and international dependencies directly influence technological deployment and industrial competitiveness. By explicitly linking application-driven demand, technological pathways for extraction and processing, and geopolitical supply structures within a unified framework, this review provides a coherent understanding of the systemic challenges facing the REE sector and identifies key leverage points for improving the robustness and sustainability of REE supply chains in the context of the global clean energy transition.Article Citation - WoS: 2Citation - Scopus: 2A Novel Biomass-Derived Reductant for Nitric Acid Dissolution of Manganiferous Iron Ore: Comparative Assessment of Organic Reductants(MDPI, 2025-12-31) Top, Soner; Altiner, Mahmut; Vapur, Huseyin; Kursunoglu, Sait; Stopic, SreckoThis study investigates the selective dissolution of manganese from a manganiferous iron ore using nitric acid (HNO3) in the presence of various organic reductants. A series of leaching experiments was performed to evaluate the effects of temperature, reductant type, and leaching time on Mn recovery, with particular emphasis on biomass (horse dung) and tartaric acid as novel reducing agents. The dissolution behaviour of Fe, Mn, Mg, Ca, and Al was systematically examined, revealing that Mn extraction was strongly enhanced in the presence of reductants, while Fe dissolution remained below 10% under all conditions. The maximum Mn dissolution exceeded 90% at 90 degrees C using biomass and reached nearly 85%-90% with tartaric acid at elevated temperatures. Kinetic studies were conducted by applying reaction order models and the shrinking core model. The results indicated that Mn dissolution in HNO3 medium is predominantly controlled by surface chemical reaction, with Arrhenius analysis yielding activation energies of 27.74 kJ/mol for biomass and 21.26 kJ/mol for tartaric acid. These relatively low values confirm the efficiency of organic reductants in facilitating Mn reduction and dissolution. To sum up, comparison of reductant efficiency revealed that, at the lowest concentrations, the dissolution of Mn followed the sequence glucose > sucrose > oxalic acid > tartaric acid > maleic acid > biomass > citric acid > acetic acid. At the highest concentrations, the trend shifted, with citric acid emerging as the most effective, followed by tartaric acid > oxalic acid > glucose > sucrose > maleic acid > biomass > acetic acid.Article Citation - WoS: 1Citation - Scopus: 1A Comprehensive Review on the Extraction and Recovery of Lithium from Primary and Secondary Sources: Advances Toward Battery-Grade Materials(Wiley, 2025-10-20) Top, Soner; Kursunoglu, Sait; Altiner, MahmutLithium-ion battery (LIB) technologies have become indispensable to modern energy systems, driving global demand for high-purity lithium compounds. This review focuses on lithium recovery and purification strategies for battery-grade lithium carbonate (Li2CO3) and lithium hydroxide (LiOH), addressing both primary sources (brines and minerals) and secondary sources (waste materials). Industrially established processes, such as evaporation-based brine treatment and conventional metallurgical methods, are discussed alongside emerging techniques, including membrane separation, solvent extraction, and CO2-assisted precipitation. Particular attention is given to lithium precipitation mechanisms, the behaviour of co-existing ions during extraction, and the specific quality requirements for cathode material synthesis. By evaluating process scalability, environmental impact, and product purity, this review provides a comprehensive understanding of current practices and future directions. Additionally, it highlights the growing importance of lithium in the context of accelerating electric vehicle (EV) adoption, underscoring the bright and expanding future of the lithium industry.Article Citation - WoS: 30Citation - Scopus: 37Testing of 17-Different Leaching Agents for the Recovery of Zinc From a Carbonate-Type Pb-Zn Ore Flotation Tailing(Pergamon-Elsevier Science Ltd, 2021-07) Hussaini, Shokrullah; Kursunoglu, Sait; Top, Soner; Ichlas, Zela Tanlega; Kaya, MuammerThe recovery of zinc from a flotation tailing using 17-different leaching agents, including inorganic and organic acids, alkaline solutions and chelating agents, was investigated. The effects of the lixiviant type, acid concentration, leaching temperature, leaching time, and solid-to-liquid ratio on the metals dissolution were studied. The use of sulfuric acid resulted in 91% of zinc extraction with a high selectivity against lead. The major impurities of lead, iron, calcium and arsenic precipitated during the leaching process as a segnisite, beudantite, gypsum, and goethite in this lixiviant. It was seen that the addition of oxidants in sulfuric acid solution slightly increased zinc dissolution. The citric acid dissolved 90.1% of zinc along with 9.1% lead. 90% of zinc dissolution was achieved by using malic acid, and high selectivity between zinc and lead dissolutions was also observed. The citric and malic acid leach residues contained a substantial amount of segnitite, beudantite, and quartz as the major phases. In term of zinc and lead dissolution selectivity, the best inorganic agents were determined in the following order: sulfuric acid > hydrochloric acid > perchloric acid > nitric acid. With organic agents, the best zinc and lead selectivity was achieved in the following order: sulfosalicylic acid > citric acid > malic acid > formic acid > tartaric acid > ascorbic acid. The best simultaneous zinc and lead dissolutions were achieved using sodium hydroxide agent. Using 5 M sodium hydroxide at 80 degrees C and 1/10 solid-to-liquid ratio for 180 min. leaching time, 81.4% of zinc and 47.4% of lead were dissolved while leaving a considerable amount of iron in the residue. When the ammonium chloride was used as a lixiviant, the silver and zinc were taken into the leach solution. 61.3% of zinc dissolution was obtained by using 50% ammonia as lixiviant, whereas no iron and lead dissolutions were observed. Using 0.37 M EDTA at 80 degrees C, 1/10 solid-to-liquid ratio for 180 min. leaching time, more than 90% of zinc dissolved along with a substantial amount of iron, arsenic and lead co-dissolutions. 47.4% of zinc dissolution was obtained at 80 degrees C and 1/10 solid-to-liquid ratio for 180 min. leaching time when sodium citrate was used as lixiviant, whereas less than 20% of zinc dissolved using ammonium oxalate at similar leaching condition. 39% zinc was dissolved using 3 M ammonium acetate at 80 degrees C, 1/10 solid-to-liquid ratio for 180 min., while 23.1% of zinc dissolution was achieved when the ammonium acetate was tested under similar experimental conditions. As a result, sulfuric, citric, malic, sulfosalicylic and formic acids were deemed to be the most promising leaching agents for the selective recovery of zinc from the lead-zinc flotation tailing.Article Citation - WoS: 62Citation - Scopus: 68Solvent Extraction Process for the Recovery of Nickel and Cobalt From Caldag Laterite Leach Solution: The First Bench Scale Study(Elsevier Science Bv, 2017-05) Kursunoglu, Sait; Ichlas, Zela Tanlega; Kaya, MuammerA solvent extraction application consisting of two-sequential solvent extraction circuits to separate the nickel and cobalt from a synthetic sulphate leach solution which simulates a typical Caldag lateritic leach solution was conceived and experimentally explored. The first circuit allowed the simultaneous extraction of most of the nickel (98%), cobalt (98%) and manganese (94%) with 20% neodecanoic acid (Versatic 10) and 5% tri-n-butyl phosphate (TBP) in ShellSol 2046 at pH 72 together with substantial amounts of calcium (65%) and magnesium (12%). Three stages of scrubbing at pH 5.6 using diluted sulphuric acid solution allowed the removal of most of the magnesium (90%) and substantial amount of calcium (16%). Complete stripping of nickel, cobalt, manganese, magnesium and calcium was achieved at pH 0.75. This loaded strip solution was the feed for the second circuit. The use 15% bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex 272) and 5% TBP in ShellSol 2046 allowed the extraction of most of the cobalt (94%) and manganese (98%) at pH 5.0 but with substantial co-extraction of magnesium (41%) and calcium (40%) and a minor amount of nickel (3%). A two-stage scrubbing of this loaded organic with cobalt (20 g L-1) solution was performed. Magnesium, calcium and nickel were completely displaced with cobalt. Most of the manganese (93%) was removed from the organic. Complete stripping of the cobalt and manganese in the scrubbed organic phase was achieved at pH 1.0. Therefore, nickel (94%) and cobalt (91%) were totally separated from the feed solution. In addition, slope analyses were carried out to determine the nature of the extracted complexes of the nickel and cobalt with each extractant. Based on the experimental results, a flowsheet for the separation process is presented. (C) 2017 Elsevier B.V. All rights reserved.Article Citation - WoS: 7Citation - Scopus: 7Separation of Mn and Fe From a Manganiferous Iron Ore Using Horse Dung as Reductant: A Zero Waste Approach(Springer, 2022-01-13) Top, Soner; Altiner, Mahmut; Kursunoglu, SaitThe separation of manganese and iron from a manganiferous iron ore using horse dung (biomass) as reductant was investigated in a sulfuric acid solution, and 99.80% Mn and 17.76% Fe were extracted into the solution under these leaching conditions: 1 M sulphuric acid concentration, 120 g/L biomass, 1/10 solid to liquid ratio, 300 rev/min stirring speed, 90 degrees C leaching temperature, and 3 h leaching time. In the first precipitation step, the iron and aluminum were first rejected from the solution at pH 5.04. Thereafter, 98.58% Mn was precipitated at pH 10 in the second step. The precipitate was identified as a pyrochroite mineral. After the leaching, the residue was subjected to a carbothermal reduction process conducted at 700 degrees C for 10 min in the presence of no extra reductant. The residue was converted to magnetite mineral, which can be easily recovered by magnetic separation. Based on the experimental results, a flowsheet has been proposed.Article Citation - WoS: 5Citation - Scopus: 5Selective Leaching of a Mixed Nickel-Cobalt Hydroxide Precipitate in Sulphuric Acid Solution With Potassium Permanganate as Oxidant(Taylor & Francis inc, 2020-10-12) Hussaini, Shokrullah; Ichlas, Zela Tanlega; Top, Soner; Kursunoglu, Sait; Kaya, MuammerSelective leaching of a mixed nickel-cobalt hydroxide precipitate was investigated using potassium permanganate as oxidant in sulfuric acid solution. 94.9% Ni, 50% Co and 0.6% Mn were dissolved under the following conditions: sulfuric acid concentration of 0.75 M, potassium permanganate of 5 g/L, temperature of 30 degrees C, leaching duration of 60 min, solid-to-liquid ratio of 1/10, and stirring speed of 400rpm. The pregnant leach solution was subjected to a solvent extraction process. 98% Co and 99% Mn were extracted at pH 4.84 with 30% (v/v) Cyanex 272, leaving essentially all nickel in the raffinate. Based on the experimental results, a flowsheet is proposed.Article Citation - WoS: 37Citation - Scopus: 44Selection of an Appropriate Acid Type for the Recovery of Zinc From a Flotation Tailing by the Analytic Hierarchy Process(Elsevier Sci Ltd, 2021-02) Kursunoglu, Sait; Kursunoglu, Nilufer; Hussaini, Shokrullah; Kaya, MuammerThe selection of acid type for metal dissolution from minerals is an important issue in leaching operations. Acids are used to recover valuable elements from the minerals by dissolving them in a solution. The acid must offer a high recovery at marginal cost and a low environmental effect. Many parameters can affect the acid type selection for high leaching recovery and low environmental effect and thus, the selection of an acid type is complex. In this study, based on the experimental results obtained from the bench-scale laboratory studies, the selection of acid type for the recovery of zinc from a flotation tailing was investigated using the analytic hierarchy process (AHP). The utilization of AHP was supported by the use of ExpertChoice (R) 2000 software. The outcomes demonstrated that sulfuric acid is the most desirable acid type with a ranking of 0.541, tracked by citric acid, and oxalic acid with scoring of 0.282 and 0.177, respectively. Furthermore, analyses of sensitivity were performed to examine the influence of the main criteria on the different acid type. It emerged that citric acid can be used when the environmental main criterion ascended from 7.8% to 75.3%. (C) 2020 Elsevier Ltd. All rights reserved.Article Citation - WoS: 7Citation - Scopus: 7Recovery of Lithium From Spent Coin-Type Lithium Manganese Dioxide Cr Cells by Acidic Leaching in the Presence of Potassium Permanganate as Oxidant(Springer, 2022-09-20) Kursunoglu, Sait; Top, Soner; Altiner, Mahmut; Ozsarac, Safak; Kaya, MuammerThe selective leaching of lithium from spent coin-type lithium manganese dioxide CR cells by oxidative leaching and precipitation of Li2CO3 from Li-bearing leach solution has been experimentally and theoretically investigated. The oxidative leaching experiments were carried out using sulfuric acid in the presence of potassium permanganate (KMnO4). The dissolutions of lithium, manganese, nickel, and cobalt were found to be 84.8%, 0.9%, 46.6%, and 9.7%, respectively. The results demonstrated that a considerable amount of manganese and cobalt remained in the leach residue. The Li-bearing leach solution was fed to an impurity removal stage. It was observed that a substantial amount of lithium loss, along with manganese, nickel, and cobalt, was determined at pH 10. At standard temperature and pressure, the species of lithium as a function of pH, lithium concentration, and carbonate concentration was evaluated for the generation of Li2CO3 from the oxidative leach solution. The results revealed that the precipitation of lithium as lithium carbonate is thermodynamically feasible from the solution at high pHs.Article Citation - WoS: 4Citation - Scopus: 3Recovery of Vanadium and Nickel From a High Caco3 Containing Petroleum Coke Ash by Roasting and Acidic Leaching(Springer, 2023-11-08) Yurtseven, Ozgun; Ibrahim, Ahmedaljaali Ibrahim Idrees; Top, Soner; Kursunoglu, Sait; Altiner, MahmutIn this study, it was aimed to extract vanadium (V) and nickel (Ni) from a petroleum coke ash (PCA) using a roasting process without additives, followed by leaching with sulfuric acid (H2SO4). The experiments were designed based on the Taguchi approach, taking into account the parameters of temperature, acid concentration, time, and solid ratio. Additional leaching tests were conducted on the non-roasted PCA for comparison, to assess the effect of roasting on the extractions of V and Ni. The results showed that no extra reducing agent was needed as the PCA contained high levels of CaCO3, which could be used as a reducing agent during roasting. It was found that roasting was essential for high Ni extractions, but had no strong effects on V extractions. The Ni extraction was found to be between 13.3 and 80.8% for the non-roasted PCA and between 43.6 and 99.3% for the roasted PCA. The V extraction was between 36 and 97.9% for the non-roasted PCA and between 45.4 and 99.9% for the roasted PCA. The optimal leaching conditions were determined to be a sulfuric acid of 4.5 M, a solid ratio of 10%, a temperature of 75 degrees C, and a time of 75 min. In addition, it was determined that the leaching conditions had a great effect on the oxidation state of vanadium ions, and an increase in the acid concentration led to the formation of V3+ ions (green color) instead of VO2+ ions (blue color) in the pregnant leach solution. The final pregnant leach solution containing 1056.50 mg/L V, and 251.85 mg/L Ni was achieved with an extraction yields of > 98%. The experimental results were greatly fitted by the shrinking core model and the activation energy (E-a) for V and Ni was calculated as 3.60 and 4.01 kJ/mol, indicating that the leaching mechanism can be explained by the diffusion control model.
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