Precious Metals Research Articles

Spatial distribution, ecological and human health risks of potentially toxic elements (PTEs) in river Ravi, Pakistan: A comprehensive study

Significant quantities of potentially toxic elements have been and are still being discharged into Pakistan's rivers through natural sources and anthropogenic activities. The present study provides a comprehensive study of potentially toxic element contamination in the water and sediment of the Ravi River, Pakistan. The research aims to examine the extent of pollution, its ecological risks, and the potential human health impacts through detailed geospatial analysis and statistical correlation. Water and sediment representative samples were taken and analyzed for potentially toxic elements, including Cobalt (Co), Cadmium (Cd), Zinc (Zn), Nickel (Ni), Arsenic (As), Chromium (Cr), Lead (Pb), Copper (Cu), and Manganese (Mn). Various pollution indices, such as the “Geo-accumulation Index (Igeo), Modified degree of Contamination (mCd), Nemerow comprehensive pollution index (Pt), Contamination factor (CF), Enrichment factor (EF), Pollution Load Index (PLI), and Potential Ecological Risk Index (PERI),” were calculated to determine the contamination levels and ecological risks. The results indicated significant spatial variability in metal concentrations, with higher levels observed in industrial and urban areas (near Lahore). Cd and As were identified as the most critical pollutants, exhibiting high Igeo, CF, EF, and PERI values. The PLI revealed that several regions along the river are heavily polluted. Pt shows high comprehensive pollution near Lahore and moderate to high pollution in surrounding areas. According to mCd, most of the study area, especially sampling points near Lahore, ranges between 8 and 16, indicating a high degree of pollution. The Human Health Risk (HHR) assessment, considering ingestion, inhalation, and dermal contact pathways, highlighted that children are particularly vulnerable, showing higher Hazard Quotient (HQ) and Hazard Index (HI) values for several metals. Correlation analysis revealed significant relationships between certain metals, suggesting common sources of contamination, likely from industrial discharges and urban runoff. The comprehensive mapping and statistical analysis underscore the urgent need for implementing effective pollution control measures to mitigate the risks posed by potentially toxic element contamination in the Ravi River. This study provides critical insights for policymakers and environmental managers to prioritize areas for remediation and to develop strategies to protect both ecological and human health in the region.

How do Carbon Emissions Spillovers Reshape Metal Market Dynamics? Time– Frequency Insights on Precious and Non-precious Metals

Global disruptions, such as health crises and geopolitical tensions, significantly impact both climate and commodity dynamics. This study, well-grounded on environmental finance theory, input–output modelling, socio-transition philosophy and behavioural finance perspectives, explores the evolving interactions between carbon emissions (CE) and metal markets during COVID-19 pandemic and Russia–Ukraine war (RUW). The study uses time-varying parameter vector autoregressive model (TVP-VAR) technique to evaluate time and frequency varying connectedness between CE and metal markets from 3 January 2020 to 28 June 2024. During the COVID-19 pandemic, initial connectedness among selected markets peaked at 85%, averaging 46%, highlighting a significant CE–metal nexus that necessitates strategic responses. In the RUW period, connectedness averaged 47.82%. CE influence metal markets primarily in the short term. Wavelet coherence analysis reveals that palladium and platinum are highly sensitive to CE over the long term, while gold and silver may serve as effective diversifiers and hedges against carbon-related risks in metal investments. The study is relevant for investors in the metal sector with environmental considerations. JEL Classifications: G110, Q430, L720

Serpentinised Dunites of the Neoarchean Shimoga Greenstone Belt, Western Dharwar Craton, India: Insights on Ni‐PGE Mineralisation and Genesis

ABSTRACTUltramafic rocks of the Archean greenstone belts worldwide are potential hosts for Cu‐Ni, precious metal deposits like platinum group elements (PGEs) and gold. This study highlights the geochemical evidence and genesis of Ni‐PGE mineralisation in the ultramafic rocks of Shimoga greenstone belt of the Western Dharwar Craton, India. Petrographically, the studied rocks are identified to be serpentinised dunites, while their geochemical signatures indicate komatiitic affinity. Presence of disseminated sulphides and pronounced serpentinisation in these rocks suggest a combination of Type II (disseminated sulphides) and Type IV (post‐magmatic alterations) komatiite‐related Ni–Cu‐PGE deposits. Chondritic Al2O3/TiO2 (9.65–16.38) ratios, superchondritic Gd/YbN (1.3–1.6), depleted high‐field‐strength elements (HFSEs) (Zr, Hf), enrichment of LREE over HREE and negative Nb–Ta anomalies reflect the generation of parental melts from plume‐sourced Al‐depleted komatiites with significant crustal contamination during their emplacement. The major, trace element and PGE relationships (FeO vs. MgO, Cu vs. Pd, Ni/Cu vs. Pd/Ir) infer the origin of sulphur undersaturated primary melts through moderate to higher degrees of partial melting followed by crustal assimilation that led to PGE enrichment. These observations suggest their formation from melts derived from greater depths of the upper mantle (> 400 km) at high pressure (> 10 GPa), wherein, the mantle residue retained majorite garnet. The high Ni (avg. Ni = 6511 ppm) substantiated by high Kambalda ratio ([Ni:Cr] × [Cu:Zn] = 5.6), Ni/Cr ratios (> 1) with high concentration of PGEs (avg. ∑PGE = 3078 ppb) confirm the fertile/mineralised nature of the komatiitic source and potential Ni‐PGE mineralization in the ultramafic rocks of the Shimoga greenstone belt.

Out-of-plane coordination of iridium single atoms with organic molecules and cobalt-iron hydroxides to boost oxygen evolution reaction.

Advancements in single-atom-based catalysts are crucial for enhancing oxygen evolution reaction (OER) performance while reducing precious metal usage. A comprehensive understanding of underlying mechanisms will expedite this progress further. Here we report Ir single atoms coordinated out-of-plane with dimethylimidazole (MI) on CoFe hydroxide (Ir1/(Co,Fe)-OH/MI). This Ir1/(Co,Fe)-OH/MI catalyst, which was prepared using a simple immersion method, delivers ultralow overpotentials of 179 mV at a current density of 10 mA cm-2 and 257 mV at 600 mA cm-2 as well as an ultra-small Tafel slope of 24 mV dec-1. Furthermore, Ir1/(Co,Fe)-OH/MI has a total mass activity exceeding that of commercial IrO2 by a factor of 58.4. Ab initio simulations indicate that the coordination of MI leads to electron redistribution around the Ir sites. This causes a positive shift in the d-band centre at adjacent Ir and Co sites, facilitating an optimal energy pathway for OER.

An Electron Bridge of Shared Atoms Mediated Cs3Bi2Br9/Bi2WO6 Z‐Scheme Heterojunction for Photocatalytic CO2 Reduction

AbstractConverting clean solar energy into chemical energy through artificial photosynthesis is an effective solution to solve the energy and environmental issues. Here, we report a Cs3Bi2Br9/Bi2WO6 (CBB/BWO) Z‐scheme heterojunction constructed via electrostatic self‐assembly, which facilitates efficient separation of photogenerated carriers and ensures the corresponding redox capacity of both components. By sharing Bi atoms, a Br−Bi−O bond is established between CBB and BWO, serving as an “electron bridge”. The electrons generated by BWO are efficiently channeled to CBB through the heterojunction‐formed “electron bridge”, thereby achieving effective photocatalytic CO2 reduction. Under simulated sunlight conditions, it exhibits the highest CO yield of 72.52 μmol g−1 (without the addition of any precious metal, photosensitizers or sacrifices), which is approximately 7‐fold and 18‐fold greater than that of pure CBB and BWO, respectively. This work provides a more profound comprehension of the regulation of electron transfer through interfacial chemical bonds, thereby proposing a promising strategy for the development of efficient heterojunction photocatalysts for CO2 photoreduction.

Potential for the Recovery of Selected Metals and Critical Raw Materials from Slags from Polymineral Zn–Pb Ore Metallurgy—Part I

Slags from the Silesia–Cracow Upland (Poland), including ten historical slags (deposited in waste dumps) and four contemporary slags (from current production), were examined to compare their chemical and mineralogical properties as well as to assess their potential for the recovery of selected metals and critical raw materials. The historical slags associated with the smelting of polymetallic ores originating from Mississippi Valley-type (MVT) deposits consisted primarily of gypsum. The contemporary slags, obtained from industrial waste rich in zinc and lead, were predominantly spinels (magnesium-aluminate and ferric) that exhibited higher iron content (up to 46.6 wt% of Fe2O3) compared to the historical slags (up to 26.1 wt% of Fe2O3). The zinc content was similar for both the slag types (3.5 wt% Zn). The average titanium and arsenic contents in the old and contemporary slags were at the same level as well, with 0.21 wt% (Ti) and 0.13 wt% (As), respectively. The contemporary slags contained higher levels of critical raw materials, such as cobalt, nickel, copper, and manganese, compared to the historical slags. Rare earth elements (REEs) were also more abundant in the contemporary slags, with an average content of 212 ppm, while the historical slags averaged 124 ppm. These findings underscore the potential for recovering valuable metals and critical raw materials from such slags, presenting opportunities for resource optimisation and environmental management.

Boosting Reactive Oxygen Species Generation via Contact‐Electro‐Catalysis with FeIII‐Initiated Self‐cycled Fenton System

AbstractContact Electro‐Catalysis (CEC) using commercial dielectric materials in contact‐separation cycles with water can trigger interfacial electron transfer and induce the generation of reactive oxygen species (ROS). However, the inherent hydrophobicity of commercial dielectric materials limits the effective reaction sites, and the generated ROS inevitably undergo self‐combination to form hydrogen peroxide (H2O2). In typical CEC systems, H2O2 does not further decompose into ROS, leading to suboptimal reaction rates. Addressing the generation and activation of H2O2 is therefore crucial for advancing CEC. Here, we synthesized a catalyst by loading the dielectric material polytetrafluoroethylene (PTFE) onto ZSM‐5 (PTFE/ZSM‐5, PZ for short), achieving uniform dispersion of the catalyst in water for the first time. The introduction of an FeIII‐initiated self‐cycling Fenton system (SF‐CEC), with the synergistic effects of O2 activation and FeIII‐activated H2O2, further enhanced ROS generation. In the FeIII‐initiated SF‐CEC system, the synergistic effects of ROS and protonated azo dyes enabled nearly 99 % degradation of azo dyes within 10 minutes, a sixfold improvement compared to the CEC system. This represents the fastest degradation rate of methyl orange dye induced by ultrasound to date. Without extra oxidants, this system enabled stable dissolution of precious metals in weakly acidic solutions at room temperature, achieving 80 % gold dissolution within 2 hours, 2.5 times faster than similar CEC systems. This study also corrects the unfavorable perception of CEC applications under acidic conditions, providing new insights for the fields of dye degradation and precious metal recovery.

Perception of Women Towards Investment in Different Investment Alternatives

Women are empowered to take active participation in investment activities through financial education and an inclusive investment environment. Several alternatives to investing are available, including mutual funds, real estate, precious metals, savings accounts, and stocks, which offer potential returns through regular income or capital appreciation. Investment alternatives are differentiated by their unique features, risks, returns, and ease of management. Investors, before investing, must take these features into account in relation to their risk tolerance, goals, and time horizon when considering any particular alternative. As women are recognized for making risk-averse investment decisions, their investments are impacted by numerous factors. The primary goal of this study is to understand the investment perception of women towards different investment alternatives. While the main factors influencing investment decisions are return, risk, and liquidity, several other factors specifically influence women investors, such as social and cultural norms, peers, and family members. Primary data was collected through a well-structured questionnaire consisting of Likert scale questions. SPSS software was used for data analysis. The initial results of the survey showed that 70% of the respondents had an average understanding of different investment options, whereas only 5% had high knowledge of different investment alternatives. When it comes to interest in a particular investment, mutual funds are the most preferred alternative. Additionally, 72% of women respondents show a moderate level of risk tolerance among all respondents in the study.

RELATION BETWEEN δ13С, δ18О AND REE CONTENT IN CARBONATITES OF THE TOMTOR COMPLEX, SAKHA REPUBLIC (YAKUTIA)

The paper reports the comprehensive study of phosphorus-rare metal (polymineral) carbonatites (I) and rare metal (ankerite) carbonatites (II) of the Tomtor massif based on ICP-MS, XRF, XRF-SI, SEM methods and isotope determination of C, O and 86Sr/87Sr. With a similar mineral composition, the REE+Y content in carbonatites (I) averages 0.38 wt. %, and in carbonatites (II) it is 1.3 wt. %. The δ18О-δ13С diagram provides the C and O isotopic compositions of carbonatites (I) and (II) as two intersecting trends: (I) carbonates from wells 4041, 6151, 115-117 represent the secondary generation of carbonates derived with the deuterium fluid involved; (II) depicts transformation of carbonate by low-T fluid, with fluid/rock ratio = 5. The study identified an increase in the REE and δ18O contents in carbonatites as the temperature of their formation decreases and enrichment of rocks with REE minerals, associated with REE mobility reduction in the fluid while the temperature is decreasing.

Mechanism Insight into Direct Amidation Catalyzed by Zr Salts: Evidence of Zr Oxo Clusters as Active Species.

The capricious reactivity and speciation of earth-abundant metals (EAM) hinder the mechanistic understanding essential to boost their efficiency and versatility in catalysis. Moreover, metal's solution chemistry and reactivity are conventionally controlled using organic ligands, while their fundamental chemistry in operando conditions is often overlooked. However, in this study, we showcase how a better understanding of in operando conditions may result in improved catalytic reactions. By assessing the composition and structure of active species for Zr-catalyzed direct amide bond formations under operating conditions, we discovered zirconium oxo clusters form quickly and are likely active species in the reactions. Formation of these clusters dismisses the use of additional organic ligands, inert atmosphere, anhydrous solvents, or even water scavenging to provide amides in good to excellent yields. More specifically, dodeca- and hexazirconium oxo clusters (Zr12 and Zr6, respectively) rapidly form from commercial, readily available Zr salts under reaction conditions known to afford amides directly from nonactivated carboxylic acid and amine substrates. Extended X-ray absorption fine structure (EXAFS) experiments confirm the presence of oxo clusters in solution throughout the reaction, while their key role in the mechanism is supported by an in-depth computational study employing density functional theory (DFT) and molecular dynamics (MD) methods. These results underline the value of (earth-abundant) metals' intrinsic solution chemistry to transformative mechanistic understanding and to enhance the sustainability of organic transformations.

Shift from legacy to emerging per- and polyfluoroalkyl substances for watershed management along the coast of China

Per- and polyfluoroalkyl substances and their short-chain alternatives have attracted world-wide attention due to their widespread presence and persistence in the environment. However, the sources, environmental fate, and driving forces of PFAS in coastal ecosystems remain poorly understood. In this study, the spatial distribution, source apportionment, and driving mechanisms of PFAS were investigated through a comprehensive analysis of water samples collected along the China's coastline. The concentrations of Σ25PFAS in water samples followed a general pattern, with higher levels observed in northern coastal zones of China than the south, ranging from 0.72 to 1872.21 ng L−1. PFOA and PFBA were dominant. Emerging short-chain PFAS, such as PFBS, PFBA, F-53B and GenX, were frequently detected, with detection rates of 97%, 99%, 95% and 77%, respectively. This indicated a shift in coastal PFAS contamination from legacy compounds to emerging short-chain alternatives. Source apportionment using the Positive Matrix Factorization model identified key contributors to PFAS pollution, including textile production, volatile precursors, precious metal industries, aqueous film-forming foam, metal-plating, electrochemical fluorination, and fluoropolymer manufacturing. Additionally, PFAS concentrations were significantly positively correlated with cultivated land, urban area, and wastewater discharge, while negatively correlated with annual precipitation and woodland coverage (p < 0.05). Socio-economic development was identified as a major driver of PFAS emissions, while the hydrological factors and vegetation coverage can significantly enhance watershed resilience against PFAS pollution.

Exploring the Potential of Bimetallic PtPd/C Cathode Catalysts to Enhance the Performance of PEM Fuel Cells.

Bimetallic platinum-containing catalysts are deemed promising for electrolyzers and proton-exchange membrane fuel cells (PEMFCs). A significant number of laboratory studies and commercial offers are related to PtNi/C and PtCo/C electrocatalysts. The behavior of PtPd/C catalysts has been studied much less, although palladium itself is the metal closest to platinum in its properties. Using a series of characterization methods, this paper presents a comparative study of structural characteristics of the commercial PtPd/C catalysts containing 38% wt. of precious metals and the well-known HiSpec4000 Pt/C catalyst. The electrochemical behavior of the catalysts was studied both in a three-electrode electrochemical cell and in the membrane electrode assemblies (MEAs) of hydrogen-air PEMFCs. Both PtPd/C samples demonstrated higher values of the electrochemically active surface area, as well as greater specific and mass activity in the oxygen reduction reaction in comparison with conventional Pt/C, while not being inferior to the latter in durability. The MEA based on the best of the PtPd/C catalysts also exhibited higher performance in single tests and long-term durability testing. The results of this study conducted indicate the prospects of using bimetallic PtPd/C materials for cathode catalysts in PEMFCs.

Aging Retardation of Lead-Acid Batteries by Adjusting Charge Controller Threshold Values in Off-grid Photovoltaic System

Hybrid systems or coupled power plants with energy storage are becoming more and more popular due to the rising need for energy. Researchers have been conducting several experiments to assure longer-lasting battery use due to the increasing widespread use of energy storage and the depletion of resources such as silicon and precious metals. In this study, a simulation study is carried out in PVSyst software on lead-acid batteries, which have a low cycle and a very traditional electrochemical structure. The simulation is realized by scaling Spain’s consumption curve in 2023, taken from the European Network of Transmission System Operators for Electricity (ENTSO-E), together with lead acid batteries and off-grid photovoltaic (PV) modules. After the off-grid system design is created and consumption data is imported, it is aimed to extend battery life by changing the charge-discharge threshold values of the charge controllers. Threshold values are in two categories, high and low, and seventeen different cases are simulated. According to the results of the simulation, the state of charge (SOC) levels of the batteries decreases significantly due to radiation and cloudiness in the winter months and remain high in the spring and summer months. When charge controllers are set to high thresholds levels, they cause gassing currents that rise to an average of 20 amps, while battery life extends up to 5.3 years. When low threshold values are used, negligible levels of oxygen and hydrogen gasses are formed in the battery, but battery life decreases to 4.1 years.

Porous N-Doped Carbon-encapsulated Iron as Novel Catalyst Architecture for the Electrocatalytic Hydrogenation of Benzaldehyde.

Carbon porous materials containing nitrogen functionalities and encapsulated iron-based active sites have been suggested as electrocatalysts for energy conversion, however their applications to the hydrogenation of organic substrates via electrocatalytic hydrogenation (ECH) remain unexplored. Herein, we report on a Fe@C:N material synthesized with an adapted annealing procedure and tested as electrocatalyst for the hydrogenation of benzaldehyde. Using different concentrations of the organic, and electrolysis coupled to gas chromatography experiments, we demonstrate that it is possible to use such architectures for the ECH of unsaturated organics. Potential control experiments show that ECH faradaic efficiencies >70 % are possible in acid electrolytes, while maintaining selectivity for the alcohol over the pinacol dimerization product. Estimates of product formation rates and turnover frequency (TOF) values suggest that these carbon-encapsulated architectures can achieve competitive performance in acid electrolytes relative to both base and precious metal electrodes.

Fe-Catalyzed α-C(sp3)-H Amination of N-Heterocycles.

Nitrogen-heterocycles are privileged structures in both marketed drugs and natural products. On the other hand, C-H amination reactions furnish unconventional and straightforward approaches for the construction of C-N bonds. Yet, most of the known methods rely on precious metal catalysts. Herein we report a site-selective intermolecular C(sp3)-H amination of N-heterocycles, catalyzed by inexpensive FeCl2,which allows the functionalization of a wide range of pharmaceutically relevant cyclic amines. The C-H amination occurs site-selectively in α-position to the nitrogen atom, even when weaker C-H bonds are present, and furnishes Troc-protected aminals or amidines. The method employs the N-heterocycle as limiting reagent and is applicable to the late-stage functionalization of complex molecules. Its synthetic potential was further illustrated through the derivatization of α-aminated products and the application to a concise total synthesis of the reported structure for senobtusin. Mechanistic studies allowed to propose a plausible reaction mechanism involving a turnover-limiting Fe-nitrene generation followed by fast H atom transfer and radical rebound.

Fe‐Catalyzed α‐C(sp3)–H Amination of N‐Heterocycles

Nitrogen‐heterocycles are privileged structures in both marketed drugs and natural products. On the other hand, C–H amination reactions furnish unconventional and straightforward approaches for the construction of C–N bonds. Yet, most of the known methods rely on precious metal catalysts. Herein we report a site‐selective intermolecular C(sp3)–H amination of N‐heterocycles, catalyzed by inexpensive FeCl2, which allows the functionalization of a wide range of pharmaceutically relevant cyclic amines. The C–H amination occurs site‐selectively in α‐position to the nitrogen atom, even when weaker C–H bonds are present, and furnishes Troc‐protected aminals or amidines. The method employs the N‐heterocycle as limiting reagent and is applicable to the late‐stage functionalization of complex molecules. Its synthetic potential was further illustrated through the derivatization of α‐aminated products and the application to a concise total synthesis of the reported structure for senobtusin. Mechanistic studies allowed to propose a plausible reaction mechanism involving a turnover‐limiting Fe‐nitrene generation followed by fast H atom transfer and radical rebound.

One-pot synthesis of porous carbon nanospheres supported CuPd alloy catalysts for the hydrogenation-dechlorination of 2,3,6-trichloropyridine

Hydrogenation-dechlorination to produce 2,3-dichloropyridine is important for the next-generation pesticides. In this work, we successfully synthesized porous carbon nanospheres supported CuPd alloy nanoparticles via a simple and efficient one-pot strategy. Furthermore, by adjusting the Cu/Pd ratio and carbonization temperature, the obtained Cu2Pd1@PCNs-500-H2O2 showed the highly catalytic activity for the hydrogenation-dechlorination of 2,3,6-trichloropyridine with a conversion rate of 70.1 % and selectivity of 71.2 %. The catalyst showed outstanding catalysis performance even after five cycles. This simple and rapid one-pot strategy provides a new approach for the large-scale synthesis of efficient heterogeneous catalysts and offers an effective solution for reducing the high costs associated with precious metals.

Late devonian calc-alkaline high-k fractionated “Ferroan” I-type leucogranites (Rudny Altai)

The paper presents the geological, geochemical and isotope-geochronological studies of the Rudny Altai granitoids in the west of Central Asian Orogenic Belt (CAOB) – the front part of the Altai convergent margin of the Siberian continent. Isotopic U–Pb dating of zircons showed an age range from 367 to 363 Ma. Geochemical characteristics indicate the relevance of leucogranites to calc-alkaline high-K series (SiO2 73 wt.%, Na2O+K2O = 6.9–9 wt.%, Na2O/K2O = 0.7–1.2), with calc-alkaline and alkaline-calcic affinities (MALI = 6.32–8.41). They bear meta- to weakly-peraluminous values (A/CNK = 0.9–1.2), high Fe* index (0.84–0.97) and high fluorine (0.04–0.17 wt.%) content. Variations of HFSEs, LILEs contents, Ga/Al ratios and strong negative A/CNK-P2O5 correlation indicate their affinity with fractionated I-type granitoids. Rare metal (beryllium) mineralization is spatially and genetically related to leucogranites. It is assumed that the formation of granitoids was associated with shearing setting at the convergent margin of the Siberian continent, as a result of oblique subduction of the Irtysh-Zaisan ocean plate.

Enhancing Stability of Surface Au under Oxidizing Conditions through Reduced Bulk Au Content.

Contrary to the common assumption that a higher bulk content of precious metals facilitates the preservation of more surface noble metal by serving as a reservoir for surface enrichment, we demonstrate that a lower bulk content of Au results in a more stable arrangement of Au atoms at the surface of Cu-Au nanoparticles when exposed to an O2 atmosphere. Using ambient pressure X-ray photoelectron spectroscopy, we investigate the surface segregation and oxidation behavior of Cu-Au nanoparticles across various compositions. Our results reveal that in Au-rich nanoparticles exposed to an H2 atmosphere, surface segregation prompts the formation of a continuous Au-enriched shell, which subsequently oxidizes into a complete CuOx shell upon transitioning to an O2 atmosphere. Conversely, in Au-poor nanoparticles during H2 treatment, segregation results in the emergence of Au clusters embedded within the surface layer, persisting upon exposure to O2. This unexpected phenomenon shows that reducing the bulk content of precious metals can enhance the surface stability of noble atoms under oxidizing conditions, as further demonstrated by comparing the catalytic performance of Cu-Au nanoparticles with varying Au bulk contents in CO oxidation.

Efficiency of Penicillium sp. and Aspergillus sp. for bioleaching lithium cobalt oxide from battery wastes in potato dextrose broth and sucrose medium

Lithium-ion batteries, a primary power source, generate electronic hazardous waste at the end of their lifespan, which is a richer source of highly concentrated metals such as cobalt and lithium than those in natural resources. The waste is a potential renewable resource for the extraction of metals. Bioleaching, a process utilizing microbial activity, was used in this study to investigate the cobalt and lithium leaching efficiency from battery wastes. Two fungal strains, Aspergillus sp. strain JMET 15 and Penicillium sp. strain JMET 24 were used with different organic carbon sources (sucrose medium and potato dextrose broth) at 1 % pulp density. The sucrose medium derived a higher acid quantity and leached higher concentration of cobalt and lithium than in potato dextrose broth. Leaching efficiency by JMET 24 was higher than JMET 15. Cobalt (32.57 % and 27.19 %) and lithium (65.07 % and 40.58 %) were bioleached by JMET 24 and JMET 15, respectively, after 30 d cultivation in the sucrose medium. Lower pulp density was conducted to achieved higher leaching efficiency by JMET24, cobalt (77.87 % and 74.5 %) and lithium (99.88 % and 78.4 %) were bioleached at 0.1 % and 0.5 % pulp density, respectively. Cobalt oxide (Co3O4) was the product of the one-step recovery (leaching and precipitation) process. Cobalt was transformed from lithium cobalt oxide to cobalt phosphate-oxalate by JMET 24 in the sucrose medium. Thus, the potential of bioleaching as an effective method for recovering valuable metals from lithium-ion battery waste is demonstrated, presenting a promising approach for both waste management and resource recovery.