Precious Metals Research Articles

Separation of valuable metals from low nickel matte to prepare NiCo2O4 materials: Optimization of oxidative leaching process and improvement of electrochemical properties of materials

The economical and efficient utilization of intermediate low nickel matte has become an important goal of nickel smelting industry. In this work, an innovative process of oxidative leaching of valuable metal from low nickel matte to prepare NiCo2O4 materials was proposed based on the materials utilization of mineral. The addition method and speed of ammonium persulfate in the oxidative leaching process was investigated to improve the extraction of valuable metals. The key factors affecting the leaching of valuable metals and the optimum leaching condition were determined by orthogonal experiments, and the extraction of Ni, Cu, and Co was 92.3 %, 97.1 % and 96.6 %, respectively. The leaching mechanism was clarified and the advantages of the leaching process were compared and analyzed. The kinetics of oxidative leaching process was studied by timing sampling method, and the control model, activation energy and kinetic equation of Ni, Cu and Co leaching were determined by analyzing the data with unreactive shrinkage model. The effects of Ni:Co ratio and calcination temperature of precursor on the properties of NiCo2O4 were investigated using the leaching solution removing iron and copper as raw materials. The NiCo2O4 material with the Ni:Co ratio of 1:2 prepared by calcining precursor at 750 ℃ for 3 h has a specific capacitance of 864F/g when the current density is 1 A/g. The prepared NiCo2O4 materials show good capacitance performance and has potential to be used as capacitor electrodes. This work combines metal extraction with product materialization, which is expected to help the metallurgical industry effectively shorten the industrial production process and reduce production costs.

Mineralogical and leaching characteristics of sulfur concentrate and hot filter residue from zinc–oxygen-pressure leaching

The mineralogical properties and environmental impact of sulfur concentrate and hot filter residue produced from the zinc–oxygen-pressure leaching were studied through a series of characterization, including X-ray fluorescence (XRF), inductively coupled plasma optical emission spectroscopy (ICP–OES), X-ray diffraction (XRD), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM–EDS), particle size distribution (PSD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and thermogravimetry and differential thermal analysis (TG–DTA). Furthermore, short-term environmental activity was assessed using the toxic leaching procedure (TCLP). The results indicated that the sulfur concentrate exhibited a coarser particle size compared with the hot filter residue, primarily appearing as spindle-shaped element sulfur (S0). The hot filter residue contained spindle-shaped S0 and rod gypsum, alongside phases of sphalerite, pyrite, and copper–silver-containing phases encapsulated by S0, recovering valuable metals first requires the removal of S0. The surfaces of both sulfur concentrate and hot filter residue were composed of S, ZnS, Al-O, PbSO4, and SiO2. They exhibited thermal instability and some degree of water absorption, with vigorous burning observed at temperatures ranging from 200 °C to 380 °C. The leachates from these materials exhibited increased concentrations of elements such as zinc, lead, and cadmium surpassing permissible limits, highlighting the importance of their safe disposal for the stable production of zinc–oxygen-pressure systems.

Investigating the potential of deep eutectic solvents for metal recovery from spent lithium-ion batteries

Abstract The development of electric vehicles and portable electronic devices has increased the use of lithium-ion batteries, resulting in increased battery waste. Currently, efficient, and environmentally friendly lithium-ion battery recycling technology is needed to reduce environmental pollution due to LIB waste. Deep eutectic solvent (DES) is attracting attention as an environmentally friendly solvent that can be used in recycling processes. This research aims to obtain Co and Mn elements from recycled lithium-ion batteries using the leaching method using DES. In the DES synthesis process, ChCl is used as a hydrogen bond acceptor (HBA) and oxalic acid as a hydrogen bond donor (HBD) with an HBA/HBD ratio (1/1). Deep eutectic solvent ChCl: oxalic acid is used as a solvent in the process of leaching valuable metals from used lithium-ion batteries. The effect of temperature and time will be investigated on the leaching recovery. These variables include temperature variations (30°C, 55°C and 80°C), time variations (1,3,5,7, and 10 minutes) and S/L 1gr/50ml with a stirring speed of 1000rpm. The results showed that the leaching recovery of Co was 62.88% and Mn was 43.56% at a temperature of 80°C for 10 minutes.

Chemical abundances along the quasar main sequence

Context. The main sequence of quasars has emerged as a powerful tool for organizing the observational and physical characteristics of type-1 active galactic nuclei (AGNs). Aims. In this study, we present a comprehensive analysis of the metallicity of the gas in the broad-line region, incorporating both new data and previously published findings, to assess the presence of any trend along the main sequence. Methods. We performed a multicomponent analysis on the strongest ultraviolet (UV) and optical emission lines for a sample of 13 radio quiet quasars in the 0.009 ≤ z ≤ 0.472 redshift range, selected based on the availability of multiwavelength data. We employed UV and optical data obtained from the Hubble Space Telescope (mainly from the Cosmic Origins Spectrograph and Faint Object Spectrograph) and several ground-based observatories, respectively. We then measured ten diagnostic ratios and compared them with the prediction of CLOUDY photoionization simulations, identifying the closest photoionization solution to the data. Results. Our investigation reveals a consistent pattern along the main sequence. We observe a systematic progression in metallicity, ranging from subsolar values to metallicity levels several times higher than solar values. Conclusions. These findings underscore the fundamental role of metallicity in correlating with the main sequence of quasars. Extreme metallicity values, at least several dozen times the solar metallicity, are confirmed in low-z AGNs radiating at a high Eddington ratio, although the origin of the extreme enrichment remains open to debate.

A robust aerogel incorporated with phthalocyanine-based porous organic polymers for highly efficient gold extraction

The gold recovery from electronic waste liquid is of great significance to the recycling of precious metals and environmental restoration. Adsorption method is the preferred technique for gold recovery, but its expansion and application prospects were often limited by the workability and recyclability of common solid powder adsorbents. Herein, a solid absorbent powder (phthalocyanine-based POP, TD-POP) was integrated into chitosan/polyethyleneimine aerogel (TD-POP@CS/PEI-2) via a facile cross-linking and lyophilization strategy. As expected, TD-POP@CS/PEI-2 possessed outstanding mechanical toughness and stability, demonstrating efficient and specific adsorption for Au (III). The maximum adsorption capacity was 2169 mg g−1, higher than most of the absorbents. TD-POP@CS/PEI-2 aerogel also exhibited fast kinetics (recovery efficiency of 81.3 % within 3 h), good selectivity (recovery efficiency of 98.35 % at 10 times concentration of Al3+, Zn2+, Cu2+ Cd2+, Co2+, Ni2+, Mn2+, and Cr6+ than Au ions) and reusability (eight times). Multiple characterizations revealed the adsorption mechanism, which implied that the excellent adsorption properties of the aerogel were ascribed to the electrostatic attraction between cationic aerogel and AuCl4− anion, coordination interaction between nitrogen-containing active sites and Au (III), and reduction of Au (III) by TD-POP@CS/PEI-2 aerogel. This work provides a valuable and promising strategy to design scalable and sustainable adsorbents for capture precious metals, also promotes the development of integral adsorbent for environmental remediation.

A Study on the efficiency of organic activator application to process refractory hard-to-beneficiate raw materials

Polymetallic ores with complex mineralogical compositions pose significant challenges in flotation beneficiation, often resulting in suboptimal separation and recovery of valuable minerals. This study aims to analyse the effectiveness of alkyl benzene sulfonic acid (ABSA) as a frothing activator in improving the flotation performance and mineral recovery of polymetallic ore. It presents the results of flotation beneficiation experiments for polymetallic ore of complex mineralogical composition. Experiments were conducted on polymetallic ore samples using ABSA as the frothing activator in the flotation process. The performance was evaluated based on recovery rates and separation efficiency, comparing the results with standard floating frothing agents. The findings showed the highest efficiency of ABSA application for samples of mixed-type ores in increasing the recovery of gold, copper, zinc and lead in the collective concentrates of flotation beneficiation. ABSA activator promotes additional cleaning of fragments containing valuable metals from oxide films and coatings and the transfer of valuable metals' microparticles due to the organics' adsorption properties and the formation of metal-carbon bonds. Another effect of using this reagent is there was an increase in concentrate mass yield while maintaining the quality parameters. A similar effect was observed for beneficiation of copper ore with complex composition - copper recovery in the main concentrate increased. Selective flotation with the development of gold concentrate from hard-to-beneficiate polymetallic ore also showed a significant increase in gold recovery with ABSA pretreatment.

Novel Strategy for Efficient Recovery of CuO-Based Multiple-Metals from Copper Smelter Dust toward CO2 Electrocatalytic Reduction.

Copper smelter dust, a typical hazardous waste that is abundant in valuable heavy metals, holds the potential to be regarded as a promising resource. This study introduces a new approach that integrates chlorination roasting and cascade condensation to efficiently recover heavy metals from copper smelter dust. The findings demonstrate the successful separation of heavy metals (Cu, Pb, and Zn) as chlorides at nearly 100% efficiency while also effectively converting trivalent arsenic (As(III)) into pentavalent arsenic (As(V)) and immobilizing it in the roasting residues, thereby reducing environmental risk. Through the utilization of thermogravimetric mass spectrum analysis and thermodynamic equilibrium calculations, the chlorination process for heavy metals was investigated, revealing both direct and indirect chlorination processes. Additionally, the study resulted in the development of a CuO-based multiple-metals electrocatalyst from the oxidized roasting-recovered heavy metal chlorides, exhibiting significantly enhanced catalytic activity and faradaic efficiency for the electroreduction of CO2 into CO and CH4 compared to pure CuO electrocatalyst under similar electrocatalytic conditions. Overall, this work presents a sustainable and scalable method and new insights for addressing environmental risks while repurposing copper smelter dust.

Terbium- and samarium-doped Li2ZrO3 perovskite materials as efficient and stable electrocatalysts for alkaline hydrogen evolution reactions

The preparation of highly active, rare earth, non-platinum-based catalysts for hydrogen evolution reactions (HER) in alkaline solutions would be useful in realizing green hydrogen production technology. Perovskite oxides are generally regarded as low-active HER catalysts, owing to their unsuitable hydrogen adsorption and water dissociation. In this article, we report on the synthesis of Li2ZrO3 perovskites substituted with samarium and terbium cations at A-sites for the HER. LSmZrO3 (LSmZO) and LTbZrO3 (LTbZO) perovskite oxides are more affordable materials, starting materials in abundance, environmentally friendly due to reduced usage of precious metal and moreover have potential for several sustainable synthesis methods compared to commercial Pt/C. The surface and elemental composition of the prepared materials have been confirmed by X-ray photoelectron spectroscopy (XPS). The morphology and composition analyses of the LSmZO and LTbZO catalysts showed spherical and regular particles, respectively. The electrochemical measurements were used to study the catalytic performance of the prepared catalyst for hydrogen evolution reactions in an alkaline solution. LTbZO generated 2.52 mmol/g/h hydrogen, whereas LSmZO produced 3.34 mmol/g/h hydrogen using chronoamperometry. This was supported by the fact that the HER electrocatalysts exhibited a Tafel slope of less than 120 mV/dec in a 1.0 M alkaline solution. A current density of 10 mA/cm2 is achieved at a potential of less than 505 mV. The hydrogen production rate of LTbZO was only 58.55%, whereas LSmZO had a higher Faradaic efficiency of 97.65%. The EIS results demonstrated that HER was highly beneficial to both electrocatalysts due to the relatively small charge transfer resistance and higher capacitance values.

Solid-State Oxide Fuel Cells

Solid-State Oxide Fuel Cell (SOFC) is an efficient energy conversion device that directly covers fuel's chemical energy into electricity. With a high energy conversion efficiency, it is not limited by the Carnot cycle. Fuel adaptability is wide, clean and pollution-free, all solid structure, do not use precious metal catalyst and other advantages. It is of great significance to achieve the goal of carbon peak and carbon neutrality target in China. However, there are some problems, mainly including: conductivity, relatively low conductivity of medium-temperature solid oxide fuel cells, which limits the performance of batteries, sintering, cost, and stability. To improve the conductivity, researchers are exploring different material combinations and doping strategies to optimize the crystal structure and chemical composition of the electrolyte. Finally, the importance of the electrolyte, the role of the oxygen vacancy, the influence of the doping elements, and the balance of the performance and the cost are drawn.

Approach towards the Purification Process of FePO4 Recovered from Waste Lithium-Ion Batteries

The rapid development of new energy vehicles and Lithium-Ion Batteries (LIBs) has significantly mitigated urban air pollution. However, the disposal of spent LIBs presents a considerable threat to the environment. Recycling these waste LIBs not only addresses the environmental issues but also compensates for resource shortages and generates substantial economic benefits. Current recycling processes primarily focus on the extraction of valuable metals, often overlooking the treatment of residual waste post-extraction. This project targets the iron phosphate (FePO4) derived from waste lithium iron phosphate (LFP) battery materials, proposing a direct acid leaching purification process to obtain high-purity iron phosphate. This purified iron phosphate can then be used for the preparation of new LFP battery materials, aiming to establish a complete regeneration cycle that recovers lithium carbonate and iron phosphate from waste LFP materials for the production of LFP. The study investigates process parameters such as acid types and concentrations, leaching time, and the number of leaching cycles. The results demonstrate that, after purification, the levels of impurity metals decrease while the iron content increases correspondingly. Under optimized experimental conditions, the dilute sulfuric acid leaching rates of Al, Cu, Ca, and Ni reached 36.0%, 51.4%, 89.5%, and 90.9%, respectively. Furthermore, hydrothermal treatment in dilute phosphoric acid achieved leaching rates of 87.9%, 85.8%, 98.4%, and 99.1% for Al, Ca, Cu, and Ni, respectively. The microstructure characterization revealed significant changes in phase and grain morphology during the leaching process in dilute phosphoric acid, which are likely associated with the liberation of impurity atoms from the lattice. These findings indicate that acid leaching is highly effective in removing impurities from the iron phosphate recycled from waste LIBs.

Reflectance spectroscopy analysis and lithium content estimation in lithium-rich rocks and stream sediments: Insights from Tuanjie Peak, Western Kunlun, China

Lithium, a rare metal of strategic importance, has garnered heightened global attention. This investigation delves into the laboratory visible-near infrared and short-wavelength infrared reflectance (VNIR-SWIR 350 nm–2500 nm) spectral properties of lithium-rich rocks and stream sediments, aiming to elucidate their quantitative relationship with lithium concentration. This research seeks to pave new avenues and furnish innovative technical solutions for probing sedimentary lithium reserves. Conducted in the Tuanjie Peak region of Western Kunlun, Xinjiang, China, this study analyzed 614 stream sediments and 222 rock specimens. Initial steps included laboratory VNIR-SWIR spectral reflectance measurements and lithium quantification. Following the preprocessing of spectral data via Savitzky-Golay (SG) smoothing and continuum removal (CR), the absorption positions (Pos2210nm, Pos1910nm) and depths (Depth2210, Depth1910) in the rock spectra, as well as the Illite Spectral Maturity (ISM) of the rock samples, were extracted. Employing both the Successive Projections Algorithm (SPA) and genetic algorithm (GA), wavelengths indicative of lithium content were identified. Integrating the lithium-sensitive wavelengths identified by these feature selection methods, A quantitative predictive regression model for lithium content in rock and stream sediments was developed using partial least squares regression (PLSR), support vector regression (SVR), and convolutional neural network (CNN). Spectral analysis indicated that lithium is predominantly found in montmorillonite and illite, with its content positively correlating with the spectral maturity of illite and closely related to Al-OH absorption depth (Depth2210) and clay content. The SPA algorithm was more effective than GA in extracting lithium-sensitive bands. The optimal regression model for quantitative prediction of lithium content in rock samples was SG-SPA-CNN, with a correlation coefficient prediction (Rp) of 0.924 and root-mean-square error prediction (RMSEP) of 0.112. The optimal model for the prediction of lithium content in stream sediment was SG-SPA-CNN, with an Rp and RMSEP of 0.881 and 0.296, respectively. The higher prediction accuracy for lithium content in rocks compared to sediments indicates that rocks are a more suitable medium for predicting lithium content. Compared to the PLSR and SVR models, the CNN model performs better in both sample types. Despite the limitations, this study highlights the effectiveness of hyperspectral technology in exploring the potential of clay-type lithium resources in the Tuanjie Peak area, offering new perspectives and approaches for further exploration.

Pt nanoparticles loaded on three-dimensional porous carbon as electrocatalysts for hydrogen evolution reaction

The electrochemical catalytic hydrogen evolution reaction (HER) holds significant potential for the sustainable production of environmentally friendly hydrogen energy. Currently, the precious metal Pt is widely acknowledged as the most superior electrocatalyst. However, its limited availability and exorbitant cost impede its extensive application. In this study, low Pt-loaded three-dimensional (3D) porous carbon composites were successfully synthesized as catalysts using a template-free method and a high-temperature pyrolysis method. By evaluating the HER performance of different Pt concentrations of the catalysts Pt/C-X (X=0, 0.05, 0.1, 0.2, 0.4, 0.7 mmol) in acid solution, it was observed that the overpotential of Pt/C-0.2 reached as low as 17 mV with a significantly low Tafel slope value of 48 mV cm−2. Meanwhile, the Bilayer capacitance (Cdl) reached an impressively high value of 247.5 mF cm−2. Consequently, this also provides a promising way to enhance the catalytic performance of the loaded catalysts.

The use of precious metals in restorative dentistry

This review delves into the historical and contemporary use of precious metals in restorative dentistry, tracing the evolution from ancient practices to modern technological advancements. It underscores the critical role of metallic materials, such as gold, silver, copper, and alloys like cobalt-chromium and titanium, in dental restorations due to their superior mechanical properties, including high elastic modulus, tensile strength, and hardness. These materials are favored for their biocompatibility, corrosion resistance, and adaptability to various manufacturing processes, including casting, mechanical processing, and advanced methods like CAD/CAM, laser sintering, and welding. Despite the advent of alternative materials catering to aesthetic preferences, metals maintain their relevance in dentistry for structural components in prosthetics, demonstrating significant advancements in dental material technology. The review highlights the importance of understanding the properties and behaviors of these materials within the oral cavity to ensure the quality and durability of dental restorations. Through a comprehensive literature search and analysis of metallurgy, manufacturing, and classification, this paper presents a thorough exploration of the indispensable role of precious metals in enhancing dental health and restorative practices.

Alumina-supported multi-metal catalyst for e-waste management for reclamation of valuable products

ABSTRACT Electronic and electrical waste (e-waste) has increased exponentially due to the humungous growth in the information technology and communication sector. Many multi-metal catalysts are developed by researchers for electronic waste plastic conversion into fuel products and recovery of valuable metals. In the present study, an Alumina-supported catalyst powder with selected transition metals metal oxides was prepared to improve the yield of hydrocarbon liquids. FESEM with energy-dispersive spectroscopy, XRD and laser diffraction particle size analysis were used to characterise catalysts. The shredded e-waste chips to catalyst weight ratio was maintained from 2:1 to 10:1 and studied. The experiments were conducted with a reaction temperature range from 300°C to 500°C. The produced fuel density was 0.88 kg/L, with 0.75 liquid fuel conversion and 71.7% overall liquid fuel yield. The light gas percentage was 4–6%. NMR analysis, bomb calorimetric study and gas chromatography-mass spectroscopy of liquid fuel analysis suggest carbon chain compounds of C3–C20 hydrocarbon, indicating a mixture of petrol and diesel-like liquid products. The catalyst can be tuned to improve liquid fuel conversion. The liquid fuel product is promising for fuel use, however, upgrading treatments are needed to meet standard product specifications.

Selective extraction of chromium from chromium-bearing electroplating sludge by pressure oxidation alkaline leaching

The selective extraction of chromium (Cr) from Chromium-bearing electroplating sludge (CES) has positive significance for harmless disposal and reducing dependence on native resources. Herein, the process of pressure oxidation alkaline leaching of CES is reported. The leaching ratio of Cr was reached 89.9 % under the optimal conditions, i.e., temperature of 125℃, NaOH concentration of 1.5 mol/L, liquid-solid ratio of 10, oxygen partial pressure of 2Mpa and reaction time of 2 h, while other elements such as Cu, Ni, Fe and Zn were virtually not leached out. In addition, the concentration of NaOH required for the maximum of the leaching ratio of Cr decreased with the increase of temperature, which attributed to the synergistic effect of temperature and NaOH concentration on the solubility and diffusion coefficient of the oxidant. As the oxygen partial pressure was increased to 2 MPa, the liquid-solid ratio was raised to 10, and the reaction time was extended to 2 h, respectively, the leaching ratio of Cr reached maximum and then remained as a constant. Kinetic studies showed the leaching process of chromium was controlled by chemical reaction, and the apparent activation energy was 112.1 kJ/mol. The efficient selective recovery of Cr is of great significance to reduce the difficulty of comprehensive recovery of valuable metal elements in the CES.

Highly Selective Recovery of Gold by In Situ Magnetic Field-Assisted Fe/Co-MOF@PDA/NdFeB Double Network Gel.

There are enormous economic benefits to conveniently increasing the selective recovery capacity of gold. Fe/Co-MOF@PDA/NdFeB double-network organogel (Fe/Co-MOF@PDA NH) is synthesized by aggregation assembly strategy. The package of PDA provides a large number of nitrogen-containing functional groups that can serve as adsorption sites for gold ions, resulting in a 21.8% increase in the ability of the material to recover gold. Fe/Co-MOF@PDA NH possesses high gold recovery capacity (1478.87mg g-1) and excellent gold selectivity (Kd = 5.71mL g-1). With the assistance of an in situ magnetic field, the gold recovery capacity of Fe/Co-MOF@PDA NH is increased from 1217.93 to 1478.87mg g-1, and the recovery rate increased by 24.7%. The above excellent performance is attributed to the efficient reduction of gold by FDC/FC+, Co2+/Co3+ double reducing couple, and the optimization of the reduction reaction by the magnetic field. After the samples are calcined, high-purity gold (95.6%, 22K gold) is recovered by magnetic separation. This study proposes a forward-looking in situ energy field-assisted strategy to enhance precious metal recovery, which has a guiding role in the development of low-carbon industries.

The depressant-free flotation separation of Cu/Zn sulfide minerals with an environmentally friendly triazine-thiol collector

The depressant-free flotation separation of chalcopyrite from sphalerite in the lower alkaline (pH<10) environment will contribute to reduce carbon emission and benefit the recovery of precious metal minerals. However, it is almost impossible for traditional collectors such as xanthates due to their weak selectivity for chalcopyrite against sphalerite. In this paper, a novel triazine-thiol collector, 2-diethylamine-4-hydroxy-1,3,5-triazine-6-thiol (DEHTT), was first introduced in flotation separation of chalcopyrite from sphalerite. The micro-flotation results elucidated that in the absence of depressants, the recoveries of chalcopyrite and sphalerite from their mixture with 2.0 × 10−6 mol/L DEHTT at pH 9.45 (Na2CO3 as regulator) were 91.83 % and 28.84 %, respectively, while those with sodium isobutyl xanthate (SIBX) were 96.11 % and 78.00 % under the same conditions. In situ AFM and contact angle exhibited that DEHTT assembled on chalcopyrite surface to form lots of aggregates which increased its hydrophobicity, while an insignificant change of sphalerite surface was observed. FTIR, zeta-potential and XPS explored that DEHTT chemisorbed the Cu sites of chalcopyrite surface through its S or O atoms. The specific flotation affinity of DEHTT to chalcopyrite might contribute the cleaner recovery of copper sulfide ores with the lower carbon emission.

Nickel release from 316L stainless steel following a Ni-free electroplating cycle

Electroplating can induce nickel release even from 316L stainless steel, typically considered safe. In this work, the influence of different electroplating processes and surface treatments on nickel release was evaluated. The nickel release was tested according to the EN 1811 standard. The impact of surface roughness on nickel release was assessed by comparing polished and unpolished samples. Results indicate that internal stresses can worsen nickel release, while increasing the thickness of the precious metal layer is beneficial. To corroborate our hypothesis, it was verified that coatings obtained through physical vapor deposition (PVD), without removing the passivation layer of the steel, did not release nickel. For these reasons, we identified the main cause of nickel release as the combined effect of the removal of the passivation layer of stainless steel and the microporosity of the electroplating process.

Assessment of an eco-efficient process for the optimization of metal recovery in lithium cobalt oxide and lithium nickel manganese cobalt oxide batteries

The expansion of technology motivates the increase of global demands for critical minerals. In this context, the exploration of secondary sources of these components is expanding. End-of-life batteries can be seen as potential sources of lithium, cobalt, nickel and manganese for electric vehicles or diverse applications in electronic equipments. This paper provides a comprehensive evaluation of the recovery of metals from waste batteries with diverse chemistry composition. Lithium cobalt oxide (LCO) and lithium nickel cobalt manganese oxide (NMC) batteries were co-treated with polyvinyl chloride (PVC) channels under supercritical water, varying reaction temperature (400–600 °C) and PVC/Battery composition (0–3 m/m) in a tubular continuous reactor. Results show high recovery rates for all metals, with up to 90% percentage recovery of lithium and cobalt in all cases. Temperature and feed composition were identified as determining factors for the recovery of lithium from LCO batteries. In the case of cobalt, temperature was identified as the most important factor that affects its recovery. The selected optimal conditions for cobalt recovery in the solid products of reactions were identified for batteries LCO and NMC: temperature of 600 °C and PVC/Battery ratio of 3.0 and temperature of 500 °C and PVC/Battery ratio of 1.5, respectively. Environmental impacts, primarily Global Warming Potential (GWP), were minimal, with 4.71·10−5 kg CO2 eq., indicating the benefits of the process as an eco-efficient and promising route for the recycling of valuable metals.

Приобретение прав собственности на природные ресурсы, содержимое недр, а также драгоценные металлы и камни, не введенные в гражданский оборот

In this article, the problem of acquiring ownership of natural resources, the contents of the subsoil, as well as precious metals and precious stones is considered. Several approaches to solving this problem have been identified in the doctrine. The author concludes that in order to acquire ownership of natural resources, the contents of the subsoil, and precious metals and precious stones that have not been put into civil circulation, it is necessary to comply with a number of requirements, which is why there is reason to believe that the acquisition of ownership of natural resources that are not publicly available for collection, precious metals and precious stones can be an independent way of acquiring ownership rights. This method is expressed in the form of obtaining a permit (license), other legal documents necessary for the nature user, as well as direct extraction (obtaining actual possession) of a natural resource. The acquisition of ownership rights to precious metals and gems introduced into civil circulation differs slightly from ordinary legal relationships and has more of an administrative-legal content than civil law.