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Solvent extraction of metals from Ti ore was investigated with a view of enhancing extraction yields by changing the concentration of the ligands, the rate of mixing, the pH, and the temperature of the solution. Norwegian Ti ore was leached with 5M HNO3 alongside 10% ascorbic acid to obtain a pregnant solution containing transition metals and some rare earth elements (REEs). Part Two of the study will address the recovery of the REEs in the ore. The elemental analysis of solid and aqueous samples was done by two models of total reflection X-ray fluorescence spectrometers (S2 PICOFOX, Bruker Corporation, Berlin, Germany; and T-STAR, Bruker Corporation, Berlin, Germany). The same analysis was repeated using an inductively coupled plasma-mass spectrometer (Perkin Elmer Sciex ELAN DRC II, Perkin Elmer, Waltham, MA, USA). The extraction process and parameters were examined by ICP-MS. The extraction efficiencies were studied under different conditions through the use of various concentrations of ligands at different pHs, temperatures, and mixing rates of the solution. At pH 1.0, 22.5 °C, and a mixing rate of 1400 rpm, the selectivity of 150 g/L trioctyl methyl ammonium chloride (Aliquat 336) was 99% Ti4+, 94% V4⁺, and 82% Hf4+, while 99% of Co2⁺ was recovered at pH 0.8. The extraction efficiency of triethyl phosphate (10% TEP) was 58% Cu2⁺, 68% Mn2⁺, and 63% V4⁺ at 55 °C, 1400 rpm, and without a pH change. Tributyl phosphate (10% TBP) was able to retrieve 87% Cu2⁺ and 78% Zn2⁺ at pH 1.3, 1400 rpm, and 22.5 °C, and 80% Ti4+ at pH 1.2. A 10% solution of 2,4,6-tris (allyloxy)-1,3,5-triazine (TAOT) demonstrated 61% Mn2⁺ and 56% Hf4+ extraction at pH 1.3, 22.5 °C, and 1400 rpm. Under the same conditions, 10% methyl salicylate (MS) was able to recover 56% Hf4+ at pH 1.3. Using 1400 rpm, di (2-ethylhexyl) phosphoric acid (10% D2EHPA) was found to selectively extract 87% Hf4+ at 22.5 °C without a pH change, and around 99% Co2⁺, Ti4+, and Fe2⁺ at pH 1.3. This study provides valuable insights into optimizing solvent extraction conditions for transition metals' recovery and serves as a precursor to future research on the extraction of REEs from Ti ores. This process is relevant from the environmental and economic perspectives since it provides the best approach to recycling metals to reduce the rate of raw ore mining. [ABSTRACT FROM AUTHOR]

With advancements in hardware and software, non-destructive radiometric analytical methods have become popular in a wide range of applications. A typical case is the study of the leaching process of metals from mineral ores and mine tailings. The objective of the current study was to develop a radiometric method based on neutron activation analysis (NAA), in particular, delayed gamma neutron activation analysis (DGNAA), to monitor the process of Mn and Zn leaching from Ti ore, Cu mine tailings, and Zn-Pb mine tailings. The DGNAA method was performed using a neutron source: a deuterium-tritium (D-T) neutron generator for Mn and a MARIA research nuclear reactor for Zn. Laboratory-scale Mn leaching from Ti ores, Cu tailings, and Zn-Pb tailings was investigated using delayed gamma-rays of 56Mn (half-life of 2.6 h). The dissolution efficiencies of Mn were found to increase with interaction time and HCl concentration (1 to 5 M) and to vary with the leaching temperature (22.5 to 110 °C). Such results were found to agree with those obtained by total reflection X-ray fluorescence (TXRF) spectrometry for the same samples. 65Zn (half-life of 244 days) was chosen to investigate real-time/online leaching of Zn in Ti ore, Cu tailings, and Zn-Pb tailings. During online monitoring, Zn recovery was also reported to increase with increased leaching time. After approximately 300 min of leaching, 80%, 79%, and 53% recovery of Zn in Zn-Pb tailings, Ti ore, and Cu tailings, respectively, were reported. Theoretically, developed mathematical prediction models for 65Zn radiotracer analysis showed that the spherical diffusion model requires much less time to attain saturation compared to the linear diffusion model. The results of NAA for Zn were compared with those obtained by handheld X-ray fluorescence (handheld-XRF) and TXRF analysis. The analyzed samples encompassed leached Ti ore, Cu tailings, and Zn-Pb tailings which were subjected to different conditions of leaching time, temperature, and HCl concentrations. The XRF analysis confirmed that the leaching efficiencies of Zn rise with the increase in leaching time and HCl concentration and fluctuate with leaching temperature. The developed approach is important and can be applied in laboratories and industrial setups for online monitoring of the recovery of any element whose isotopes can be activated using neutrons. The efficiency of the metal-recovery process has a direct impact on the normal operation and economic advantages of hydrometallurgy. [ABSTRACT FROM AUTHOR]

Scientifi c objective of this work was elaboration of radiometric method for the development of hydrometallurgical process for recovery of Cu from the copper ore. A neutron activation analysis (NAA) was identifi ed as a very convenient tool for the process investigation. The samples of copper ore were activated in a nuclear reactor. The parameters of the neutron activation were calculated. Radioisotope 64Cu was selected as an optimal tracer, and it was used for the investigation of the leaching process. During the experiments, various processes applying leaching media such as sulphuric acid, nitric acid, and organic acids were investigated. The recovery of the metals using sulphuric acid was insuffi cient, around 10%. Investigated organic media also did not meet expectations. The best results were obtained in experiments with nitric acid. Up to 90% of Cu and other metals were extracted from the copper ore. Copper concentration calculations obtained by NAA were confi rmed by inductively coupled plasma mass spectrometry (ICP-MS) technique. Both techniques gave comparable results, but the advantage of the NAA is a possibility for easy online measurements without shutting down or disturbing the system.

The use of radiotracers in the present study is intended to replace traditional steps of metal quantitative analysis (solution sampling and instrumental chemical analysis) and to allow real-time measurements of metal concentrations during the leaching process. In this study, 64Cu, an isotope of copper, was selected as a radiotracer. Samples of copper flotation tailings were irradiated in the Maria research reactor (Świerk, Poland) and mixed with an inactive portion of the milled fl otation waste. The leaching process was carried out in a glass reactor, and the radiation spectrum was measured using a gamma spectrometer. The material was then treated using various acids (sulphuric acid, nitric acid, acetic acid, citric acid, and ascorbic acid) in a wide range of their concentrations. Experiments with the radiotracer were conducted in sulphuric and nitric acids. The amount of the leached metal (copper) was calculated on the basis of the peak area ratio in the gamma-ray spectrum of the activated tailings and standard samples. Inductively coupled plasma mass spectrometry (ICP-MS) was also used to analyse the metal content. Maximum recovery of 56% Cu was achieved using 9 M HNO3, whereas the recovery was lowest for ascorbic acid (

Kenya is an East African country with the third-largest economy in sub-Saharan Africa. The demand for metals and minerals continues to increase due to urbanization, population rise, and new infrastructure growth in different countries. Kenya formally confirmed the discovery of oil and various minerals in April 2013, launching itself as a new player in Africa's rapidly expanding extractive sector. This review paper highlights the mining status in Kenya and the role of hydrometallurgical and flotation processes in the recovery of deficit metals from ores and mine wastes. The nation's 2030 Vision is anticipated to benefit greatly from the proceeds from the sale of oil, gas, and valuable metals. Because Kenya was originally mapped as an agricultural region, less mineral prospecting was done in earlier times. The country's mining industry is now dominated by the manufacture of non-metallic goods, and it is largely neglected for minerals. One of the most serious problems for the mining industry in Kenya is the production of tailings that hold strategic metals. The material is already ground, which means the most energy-consuming process has been already applied, and chemical engineering processes like leaching are more feasible at this point. Hydrometallurgical and flotation recovery of valuable metals from wastes, high and low-grade ores, or tailings is essential. The resources will be preserved, which ensures sustainability in the growth of the mining industry. [ABSTRACT FROM AUTHOR]

The studies of the synthesis of uranium carbide from uranyl-ascorbate gels using the complex sol-gel process (CSGP) have been carried out. The synthesis of uranyl-ascorbate mixture as liquid sol from uranium trioxide and ascorbic acid and solid gel by extraction of water from sol were carefully examined. Ascorbic acid was used as a complexing agent in complex sol-gel process and as a carbon source. The crucial step to obtain final uranium carbides from the aforementioned substrates is the carbonization process. The thermal behavior of ascorbic acid and uranyl-ascorbate gels in a nitrogen atmosphere in the temperature range of 25-900°C were investigated using TG-DTG. Furthermore, the products of the carbonization of uranyl-ascorbate gels in nitrogen, argon and vacuum atmosphere were identified by X-ray diffraction. TG-DTG was used also as a method for determining of carbon residues in the samples.