Leaching Of Lead Research Articles

Surface treatments on commercial glasses: durable impact on the retention of lead, barium and boron

Glass durability is one of the properties that can be affected by surface treatments such as coatings or chemical attacks. These treatments can be used to reduce the quantities of potentially toxic elements contained in glass that may be released in solution. Five surface treatments were selected: three different coatings (SnO2, TiO2, SiO2) and two acidic attacks (SO2 dealkalization and acid polishing). These treatments were performed on five glass compositions (soda-lime, borosilicate, barium silicate, opal, and lead crystal). Their effects on alteration rates and mechanisms were investigated through a single protocol (acetic acid 4%, 70 °C) simulating accelerated aging conditions for containers of beverages or food. The data collected over 1.3 years showed significant reduction of lead leaching with all treatments except acid polishing. The best reduction factor was obtained with SO2 dealkalization, which also demonstrated beneficial effects towards the retention of Ba by reducing the diffusion of alkalis.

Mineralization characteristics of Lead-Zinc-Copper deposits in Akdağmadeni Region (Northern Central Anatolia, Türkiye): Integration of field study, geochemical, isotope, and geophysical data

The Akdağmadeni region is one of the important Pb-Zn-Cu metallogenic provinces in Türkiye. Most of the Pb-Zn-Cu deposits in the region are located near granitoid intrusions within metamorphic rocks, and they are typically classified as skarn-type ores associated with granitoids. However, no relationship has been determined between the Başçatak prospect and any granitoid outcrop. This raises the question of whether the Pb-Zn-Cu mineralization in the region is related to granitoids or if magmatic processes remobilized pre-existing mineralization. Observations from field studies suggest that mineralization in the Başçatak prospect is a stratiform type, metamorphosed occurrence that might have occurred earlier than the granitic intrusions. The geochemical data indicated that the granitoids have low-grade, subeconomic Cu potential and no Zn productivity potential, supporting these observations. Geophysical data also show that there is no intrusive body beneath this prospect. Granitoid-related deposits (Karapir - Ortaköy and Akçakışla) exhibit two distinct occurrences around the contact between the granite and the surrounding metamorphic rocks. The first type of occurrence (O-1) is formed at the contact and contains magnetite, pyrrhotite, and chalcopyrite. The second type of occurrence (O-2) is located outside the contact and is rich in sphalerite and galena. Both O-1 and O-2 contain skarn minerals along with ore minerals. The δ34S values of sulfide minerals from the deposits range from −0,7 to 7,5 ‰ (V-CDT). These values overlap with those of both magmatic sulfur and reduced sulfur from seawater-dissolved sulfate, making it difficult to suggest a sulfur source without additional data. Lead isotope compositions of the galenas from all deposits plot above the average crustal growth curve, suggesting an upper crustal and orogenic source similar to Western Mediterranean and Türkiye type materials described in the literature for the lead, source in different time intervals. Furthermore, Pb isotope geochemistry suggests a contemporaneous age with the host metamorphic rocks (Carboniferous – Lower Permian) for the Başçatak prospect. These results support observations indicating a syn-genetic formation for the Başçatak prospect. The age range of granite-related deposits forms two sub-groups:105–77 Ma and 61–50 Ma corresponding to the Upper Cretaceous and Paleocene transition. These data indicate that that the galenas were formed in two different stages in these mineralizations. Stratiform mineralization in the Başçatak prospect likely formed either through exhalative sedimentary processes by hydrothermal fluids or through chemical sedimentary processes under reductive conditions in a marine environment during metamorphism. O-1 appears to have been formed by hydrothermal fluids developed during granitic magmatism. A plausible formation process for O-2 involves the leaching of sulfur, lead and other metals from Başçatak type enrichments in metamorphics, with transportation and deposition within the epidotized calc-schist and marbles outside the granitoid contacts. The uplift of granitic intrusions prepared the channels and depositional environment for O-2 and caused heating of the hydrothermal fluids during this mineralization period.

Enhancing pyromorphite formation through hydroxyapatite application in lead-contaminated, water-unsaturated soils: influence of low percolation velocity and high soil porosity

Abstract Purpose Chemical immobilization using hydroxyapatite (HAP) is a cost effective and environmentally sound strategy for remediating lead-contaminated soils, such as shooting range soils. Understanding the combined impact of soil chemical and physical properties on enhancing the formation of pyromorphite, a lead-insoluble phase, is crucial for mitigating environmental risks associate with contaminated soil. This study aimed to elucidate the relationship between percolation velocity and lead leaching as well as pyromorphite transformation to optimize pyromorphite formation in water-unsaturated soils. Methods Two up-flow suction percolation tests were performed: one varying percolation velocity with soil porosity achieved by incorporating clay minerals, and the other varying percolation velocity while keeping soil porosity constant. Results Application of HAP substantially suppressed lead leaching in both percolation tests. Enhanced pyromorphite formation was observed with higher percolation velocities relative to soil porosity. Pyromorphite formation was more pronounced at lower percolation velocities compared to higher velocities at equivalent soil porosity level. The percentages of lead formed as pyromorphite in HAP-treated soil were higher than those of lead leached in non-HAP-treated soil among the lower percolation velocities. Conclusions This study provides experimental evidence indicating pyromorphite formation is favored in soils with lower percolation velocities and higher soil porosities. Therefore, considering both soil chemical and physical properties is essential for understanding immobilization mechanisms in contaminated soils.

Mineralogy of Zinc and Lead Metallurgical Slags in Terms of Their Impact on the Environment: A Review

This paper presents the results of a study of the mineralogical and chemical composition of zinc and lead metallurgical slags. These slags contain numerous elements, including toxic metals, which form conglomerates or multiphase intergrowths. The phase composition of slags is one of the main factors that determine their behaviour in weathering environments, that is, their ability to release metals when exposed to atmospheric factors. In this paper, the release of elements from slags and their mobility in a hypergenic environment is determined based on the results of leachability tests and on geochemical modelling, thus assessing the environmental impact of landfilled slags. The elements released from slags in the largest quantities are zinc and lead. Zn is leached out over a long period of time. It was found that after 12 years, the concentration of Zn in the eluate exceeds by 40 times the permissible value of 200 mg/kg for hazardous waste. The degree of leaching of lead from slags as a function of time (after 12 years), despite its significant solubility in water, is much lower than the degree of leaching of zinc. The most mobile phase components of slags in the studied hypergenic environment are the lead phases (anglesite and galena) and, to a lesser extent, the zinc phases (sphalerite and willemite). Anglesite and galena in almost the entire Eh-pH range, along with admixtures of elements, decompose into ionic forms: PbCl42−, Pb2+, and PbOH+. Sphalerite in the soil and water environment (oxidizing and acidic conditions) will decompose into the mobile ionic form Zn2+. Willemite, which is resistant to weathering, will undergo similar decomposition. It can therefore be assumed that the carriers of toxic metals are primarily lead sulphides and sulphates, zinc sulphides, and, less frequently, zinc, lead, and iron oxides.

B-nZVI optimization of strength and heavy metal stability of lead-contaminated soil solidified by Portland cement.

Traditional cement solidifying or stabilizing heavy metal-contaminated sites often face issues like alkalinity loss, cracking, and poor long-term performance. Therefore, bentonite-supported nano-zero-valent iron (B-nZVI) was introduced to optimize the remediation effect of cement in this paper. The effects of B-nZVI, ordinary Portland cement (OPC), and B-nZVI + OPC on the chemical stability of heavy metals and the physical strength of lead-contaminated soil were compared using semi-dynamic leaching methods, BCR tests, unconfined strength analysis, and micro-assisted analysis. Results demonstrated that the addition of B-nZVI effectively enhanced the remediation efficacy of OPC on lead-contaminated soil. The combination of B-nZVI and OPC exhibited a synergistic repair effect, offering superior physical strength and chemical stability for lead remediation. B-nZVI facilitated the adsorption and enrichment of Pb2+, thereby reducing oxidizable lead and enhancing short-term stabilization. Meanwhile, OPC precipitation and silicate gelling stabilized exchangeable lead into the residual form, necessitating repeated hydration gelling. Additionally, B-nZVI's sealing effect via water absorption delayed the leaching of exchangeable lead, thereby reducing lead migration. Even with only 1% B-nZVI added to the 12% OPC base, the leaching amount of Pb2+ decreased significantly from 67.6 to 6.59mg/kg after 7 d of curing. The unconfined strength of contaminated soil treated with the composite solidifying agent for 7 d was 12.87% higher than that of OPC alone, and for 28 d, it was 36.48% higher. This optimization scheme presents a promising approach for effective and sustainable remediation of heavy metal-contaminated sites.

Zinc and Lead Leaching from Sphalerite-Galena Concentrate Using Deep Eutectic Solvents Based on Choline Chloride: Effect of Roasting and Iodine as Oxidizing Agent.

The traditional metallurgical routes for producing lead and zinc from primary sources have a significant environmental footprint. Thus, using less pollutant solvents, such as deep eutectic solvents (DESs), would offer a greener solution in metal extraction. This study explores the use of three DESs based on choline chloride (ChCl) (1:2 ChCl-urea, 1:2 ChCl-ethylene glycol, and 1:2 ChCl-glycerol) for recovering Zn and Pb from a sphalerite-galena concentrate of the mining region in Ecuador. Leaching tests of the concentrate (untreated and roasted at 600 °C) in each DES were conducted (30 °C-24 h). The effect of adding iodine as an oxidizing agent was also evaluated. Recoveries of 2% (Zn) and 14% (Pb) were reported when leaching the untreated concentrate with DES. These recovery values increased to 11% (Zn) and 99% (Pb) after adding iodine during the leaching of the untreated concentrate. Roasting had a similar effect on leaching, increasing the recovery values of Zn (75%) and Pb (90%). Combining roasting as a pretreatment and iodine as an oxidizing agent produced higher Zn recoveries (99%) and Pb (99%). These results were compared to recoveries in acid leaching (H2SO4 and HNO3), revealing the potential of DESs as an alternative for metal recovery from primary sources.

Selective lead capture using amide-containing COFs: A novel strategy for efficient soil remediation

A critical consideration in the application of phytoremediation to remediate sludge soil contaminated with heavy metals is the potential for leaching risks that prevail prior to the efficient uptake of these metals by plants. The most cost-effective method is to use heavy metal stabilizers with selective adsorption. A novel amide-based COF material (COF-TH) has been synthesized as a heavy metal stabilizer for Pb. COF-TH exhibits significant selectivity for Pb in five-metal-mixed solutions, with a distribution coefficient KD as high as 3279 mL·g–1, which was more than 7.3 times that of other heavy metals. The maximum adsorption capacity of COF-TH for Pb was 189 mg·g–1. The adsorption fitted Langmuir model and intra-particle diffusion model, and satisfied pseudo-second-order kinetic model. The excellent selectivity and adsorption performance originate from the complexation between abundant amide groups and Pb ions. Pot experiments and leaching assays confirm that COF-TH decreased Pb leachate concentrations by 77.8 % without significantly decreasing total phytoextracted amounts of other heavy metals, due to the high selectivity of COF-TH to Pb. Additionally, its positive impact on plant growth and microbial diversity makes it a promising soil remediation agent. This investigation offers a novel approach to mitigate the leaching risk of a specific heavy metal Pb during sludge land application by integrating soil phytoremediation with stabilization techniques.

Study on the enhancement of citric acid chemical leaching of contaminated soil by modified nano zero-valent iron.

This study aimed to evaluate the effect of modified nanoscale zero-valent iron (SAS-nZVI) on chemical leaching of lead and cadmium composite contaminated soil by citric acid (CA). The synthesized SAS-nZVI was used as a leaching aid to improve the removal rate of soil heavy metals (HMs) by CA chemical leaching. The effects of various factors such as SAS-nZVI dosage, elution temperature and elution time were studied. At the same time, the effect of chemical leaching on the basic physical and chemical properties of soil and the morphology of HMs was evaluated. The results show that when the SAS-nZVI dosage is 2.0g/L, the leaching temperature is 25°C, and the leaching time is 720min, the maximum removal rates of Pb and Cd in the soil are 77.64% and 97.15% respectively. The experimental results were evaluated using elution and desorption kinetic models (Elovich model, double constant model, diffusion model). The elution and desorption process of Pb and Cd in soil by SAS-nZVI-CA fitted well with the double-constant model, indicating that the desorption kinetic process of Pb and Cd is a heterogeneous diffusion process, and the elution process is controlled by diffusion factors. After leaching with SAS-nZVI-CA, the physical and chemical properties of the soil changed little, the mobility and toxicity of HMs in the soil were reduced, and the HMs content in the leaching waste liquid was reduced. It can be concluded that SAS-nZVI enhances the efficiency of CA in extracting Pb and Cd from soil, minimizes soil damage resulting from chemical leaching technology, and alleviates the challenges associated with treating leaching waste liquid.

Selective leaching of lead from complex polymetallic sulfide secondary concentrate with ferric methanesulfonate and methanesulfonic acid solution

The selective leaching of lead from complex polymetallic sulfide secondary concentrate (CPSSC) with the solution mixed by ferric methanesulfonate and methanesulfonic acid (Fe(MS)3-MSA) was investigated by leaching experiments, analysis of solids, and electrochemical characterizations. The leaching results showed that stirring rate, liquid–solid ratio, temperature, and ferric concentration greatly influenced Pb extraction rate. At the optimum leaching conditions, 93.1 % Pb, while 3.8 % Cu and 18.8 % Fe were extracted. The selective leaching mechanism was related to the activity of PbS in Fe(MS)3-MSA solution and the galvanic effect between sulfides. XRD and SEM-EDS results of leaching residues verified the selective decreases in PbS, and retainment of most Cu, Fe, and Zn. Electrochemical characterizations demonstrated a more stable and higher open-circuit potential, and an increase/decrease in A0 peak potential/current in LSV curve for the residue’s electrode, suggesting the selective decreases in active components (e.g. PbS). After selective leaching, Cu could be easily extracted from residues by pressurized water leaching, and Fe(MS)3-MSA solution could be regenerated for recycling used in leaching. These results indicate the great potential of Fe(MS)3-MSA solution to selectively leach and separate Pb from CPSSC, and unveil a method to effectively treat refractory CPSSC.

Role of Pyrolysis Temperature on Arsenic and Lead Leaching Potential in a Biochar-Amended Sediment

Role of Pyrolysis Temperature on Arsenic and Lead Leaching Potential in a Biochar-Amended Sediment

A Direct Chemical Approach to Mitigate Environment Lead Contamination in Perovskite Solar Cells

Current guidelines indicate that the lead levels in perovskite solar cells are sufficiently low, putting them on par with the safety of other lead-containing electronics. Yet, there remains ambiguity regarding the exact environmental impact of lead derived from perovskite. When this lead enters the soil, it has the potential to permeate plants and, subsequently, our food supply, at a rate that is a staggering ten times more than other lead contaminants from human-induced activities. Given this, it becomes vital to ensure that lead does not pollute our environment as we further adopt these technologies. In this study, we propose a novel method using polymer net bones to anchor the lead, which effectively reduces the risk of lead leaching due to rainfall. Perovskite Solar Cells (PSCs) integrated with this polymer net bone show improved operational efficiency and hold significant promise in curtailing lead leakage, reinforcing the ecological integrity of perovskite solutions. When enhanced with Polyvinyl Alcohol (PVA), these PSCs register a notable increase in Power Conversion Efficiency (PCE), scoring 24.7% as opposed to the 22.3% in PSCs devoid of PVA. Additionally, PVA-augmented PSCs outperform in stability when compared to their traditional counterparts.

Managing potential environmental and human health risks of lead halide perovskite photovoltaic modules

Perovskite solar cells (PSCs) are emerging photovoltaic (PV) technologies capable of matching power conversion efficiencies (PCEs) of current PV technologies in the market at lower manufacturing costs, making perovskite solar modules (PSMs) cost competitive if manufactured at scale and perform with minimal degradation. PSCs with the highest PCEs, to date, are lead halide perovskites. Lead presents potential environmental and human health risks if PSMs are to be commercialized, as the lead in PSMs are more soluble in water compared to other PV technologies. Therefore, prior to commercialization of PSMs, it is important to highlight, identify, and establish the potential environmental and human health risks of PSMs as well as develop methods for assessing the potential risks. Here, we identify and discuss a variety of international standards, U.S. regulations, and permits applicable to PSM deployment that relate to the potential environmental and human health risks associated with PSMs. The potential risks for lead and other hazardous material exposures to humans and the environment are outlined which include water quality, air quality, human health, wildlife, land use, and soil contamination, followed by examples of how developers of other PV technologies have navigated human health and environmental risks previously. Potential experimentation, methodology, and research efforts are proposed to elucidate and characterize potential lead leaching risks and concerns pertaining to fires, in-field module damage, and sampling and leach testing of PSMs at end of life. Lastly, lower technology readiness level solutions to mitigate lead leaching, currently being explored for PSMs, are discussed. PSMs have the potential to become a cost competitive PV technology for the solar industry and taking steps toward understanding, identifying, and creating solutions to mitigate potential environmental and human health risks will aid in improving their commercial viability.

The Characterization of Residues Related to the Roasting– Leaching–Electrowinning Zinc Production Route for Further Metal Extraction

Super-hot acid leach residue is generated during zinc production in the roasting–leaching–electrowinning route, where both primary and secondary resources are used as feed material. This residue may contain valuable metals, such as lead, zinc, and iron, as well as precious metals, such as gold and silver. Four materials, namely super-hot acid leach residue, a residue formed when super-hot acid leach residue is selectively leached for lead with triethylenetetramine, as well as flotation concentrate, and flotation tailings formed in a selective silver flotation process with super-hot acid leach residue as the feed material were characterized to obtain a deeper understanding of possible further metal extraction. These four materials were characterized for chemical composition, mineralogy, and mineral distribution via chemical analyses, X-ray diffraction, and energy-dispersive scanning electron microscopy, respectively. The scanning electron microscope images showed that the materials have large variations in particle size distribution and composition. The results showed that the main lead phase in super-hot acid leach residue is lead sulfate, whereas it is mostly converted to lead sulfide during the selective lead leaching of the super-hot acid leach residue. The remaining lead sulfate is found in a solid solution with barium sulfate. Extracting lead from super-hot acid leach residue via triethylenetetramine leaching resulted in increased concentrations of gold and silver by 41% and 42%, respectively. The identified silver phases in super-hot acid leach residue may correspond to silver sulfide, silver chloride, and elementary silver, where silver sulfide was the most commonly occurring silver phase. After leaching this selectively for lead with triethylenetetramine, similar silver phases were identified, but silver sulfide and silver chloride occurred to a similar extent. Additionally, silver copper sulfide was detected. The presence of different silver phases might pose a challenge to reaching high silver recovery during leaching as the optimum leaching conditions differ somewhat. Furthermore, elemental sulfur, with a tendency to coat gold and silver particle surfaces, which is indicated to be present in all materials except the silver flotation tailings, may hinder metal extraction.

Accelerated carbonation of waste paper fly ash by liquid process (NaHCO3) for stabilization of Ba and Pb

The increase of energy valorization of paper sludge waste and biomass due to their high calorific value by incineration leads to an increase of waste paper fly ash (WPFA) quantities, which are in most cases considered as hazardous, and must be dealt with accordingly. The Alternative options for the management of WPFA, such as stabilization/solidification, vitrification or sintering, are not fully developed or either costly. In the present study, accelerated carbonation technology was used to reduce the hazardous nature of WPFA by improving the stabilization of metallic and metalloids trace elements (MMTE), especially Barium (Ba) and Lead (Pb) leaching. The accelerated carbonation of WPFA was found to be optimal at a water/solid ratio of 0.3 L/kg under controlled temperature and humidity conditions. The use of water saturated with 25% sodium bicarbonate (NaHCO3) improved the carbonation of WPFA and the stabilization of Ba and Pb. Batch leaching tests based on thermodynamic equilibrium was used to evaluate the solubility of the MMTE as a function of pH and at the natural pH of non‑carbonated and carbonated WPFA. Thermogravimetry, X-ray diffraction, scanning electron microscopes and energy dispersive spectroscopy analyses were performed to investigate the evolution of carbonation over time and its effect on the chemical and mineralogical properties of WPFA. After 30 days of accelerated carbonation, the leaching concentration of Ba and Pb was below the French legal limit. The leaching concentration of Ba and Pb from carbonated samples decreased 99% and 99.5% respectively. The leaching and release potential behavior of carbonated WPFA were further evaluated using the four-step sequential extraction procedure proposed by the Commission of the European Communities Bureau of Reference (BCR). The speciation of MMTE underwent significant transformation, shifting predominantly from the soluble fraction to the carbonated fraction as a result of the carbonation reaction.

Recovery of lead from the leaching residue derived from zinc production plant: process optimization and kinetic modeling

ABSTRACT This study aimed to extract lead from a zinc production plant residue containing 3.67% PbO, 2.79% ZnO, 8.75% SiO2, 24.8% SO2, 2.38% Fe2O3, and 4.46% Al2O3. In this regard, response surface modeling based on the central composite design was utilized to scrutinize and optimize the operating parameters such as NaCl concentration, HCl concentration, pulp mixing rate, solid percentage, and leaching time on the leaching efficiency of lead. Our findings demonstrated that NaCl concentration and solid percentage were the most effective parameters on the leaching of lead, in which higher concentrations of chloride and lower solid contents led to an enhancement in lead recovery. To attain the maximum recovery of lead (75.72%) at room temperature, the optimum conditions were found to be 2 mol/L HCl, 350 g/L NaCl, solid percent 10%, stirring rate 300 rpm, and leaching time 90 min. The leaching kinetics was also examined based on the shrinking core models to realize the process mechanism and develop a new kinetic model. The results exhibited that the kinetics control mechanism was the product layer diffusion model with an activation energy of 16.69 kJ/mol. Finally, a kinetic model is developed based on the diffusion model and effective parameters.

A novel approach for the efficient recovery of lead from End-of-Life Silicon Photovoltaic modules

There is an urgent need to develop a technology for recycling solar waste that will soon be generated in heaps. While various studies focused on recovering valuable materials from waste silicon solar panels, there has been minimal emphasis on the treatment of toxic substance lead. Thus, the current study proposed a novel approach to treat the harmful component of lead by recovering it in its less toxic form as PbO having commercial applications. This is accomplished through optimization of a three-step process (i) selective leaching of the top layer from interconnect, (ii) extraction of lead from the leachate by precipitation, and (iii) calcination. The lead recovery at each stage was analyzed by characterization techniques viz. ICP-OES, XRD, SEM, and a unique attempt has been made to optimize the precipitation process by constructing an Eh vs. pH diagram. The efficient leaching of lead from interconnects was observed with 1.5 M nitric acid for 5 min at 60 °C which was followed by precipitation from the leachate with 1.5 M NaOH solution and finally calcination at 500 °C for 2 h to obtain lead monoxide. The feasibility of the optimized process at a larger scale was carried out with 200 g (60-cell panel) of copper ribbons.

Thiourea-assisted selective removal of arsenic from copper smelting flue dusts in NaOH solution

The selective removal of arsenic from copper smelting flue dusts is of great significance for environmental protection and resource recycling. This study employed thiourea assisted alkaline leaching to selectively extract arsenic from copper smelting flue dusts. The effects of NaOH concentration, thiourea concentration, temperature, leaching time and pulp density on the dissolution of arsenic, zinc, lead, copper and antimony in NaOH solution were studied. The results show that the addition of thiourea can effectively promote extraction of arsenic while inhibiting the leaching of zinc, lead and copper in copper smelting flue dust. Under the optimized leaching conditions, the leaching efficiencies of arsenic and antimony were 98.5% and 1.62%, respectively, while zinc, lead and copper were not leached. X-ray diffraction (XRD) analysis suggested that the addition of thiourea promoted the dissolution of insoluble arsenate minerals. The combined results of scanning electron microscopy (SEM), mineral liberation analysis (MLA), and X-ray photoelectron spectroscopy (XPS) demonstrated that thiourea prevented sulfide products from forming a coating on arsenic surface. This work has important implications for the development of processing technologies for arsenic-containing materials.

Strong magnetic and ultrasonic fields enhanced the leaching of Ga and Ge from zinc powder replacement residue

Gallium (Ga) and Germanium (Ge) are crucial strategic resources with extensive applications in high-tech industries. However, Ga and Ge primarily occur as associated minerals. The process involves the leaching of lead–zinc ores and subsequent leaching to recover the valuable elements. The conventional acid leaching procedure exhibits low leaching effectiveness for Ga and Ge, making their recovery challenging. This study initially investigated the occurrence states of Ga and Ge. The thermodynamic simulations were used to investigate the feasibility of Zinc powder replacement residue (ZPRR) in a two-stage acid leaching process. The leaching mechanism in the strong magnetic field and ultrasonic field was studied using several characterizations such as XRD, SEM, XPS, FT-IR, etc. The investigation revealed that raising the temperature in the acidic solution led to an enhanced leaching efficiency of Ga and Ge. However, at 120 °C, the leaching efficiency of Ge decreased due to the hydrolytic precipitation occurring between Ge and SiO2. Nevertheless, the utilisation of a strong magnetic field proved advantageous in impeding this process. Furthermore, the application of the combined ultrasonic field contributed to enhancing the level of residue refining, hence promoting the effectiveness and degree of the reaction. Thus, the leaching efficiency of Ga and Ge was influenced by temperature, strong magnetic field, and ultrasonic field in combination. The high leaching efficiency of 95.53 % and 97.11 % for Ga and Ge, respectively, could be attained in the optimal experimental parameters. This study offers theoretical guidance for the effective and environmentally friendly leaching of Ga and Ge. Furthermore, it has been observed that this method is also promising for leaching the other valuable metals.

A Comprehensive and Sustainable Recycling Process for Different Types of Blended End-of-Life Solar Panels: Leaching and Recovery of Valuable Base and Precious Metals and/or Elements

The production of photovoltaic modules is increasing to reduce greenhouse gas emissions. However, this results in a significant amount of waste at the end of their lifespan. Therefore, recycling these solar panels is important for environmental and economic reasons. However, collecting and separating crystalline silicon, cadmium telluride, and copper–indium–gallium–selenide panels can be challenging, especially in underdeveloped countries. The innovation in this work is the development of a process to recycle all solar panel waste. The dissolution of all metals through the leaching process is studied as the main step of the flowchart. In the first step of leaching, 98% of silver can be recovered by 0.5 M nitric acid. Then, the second and third step involves the use of glycine for base metal dissolution, followed by the leaching of valuable metals with hydrochloric acid. The effect of parameters such as the initial pH, acid concentration, solid/liquid ratio, and hydrogen peroxide concentration is studied. The results show that up to 100% of Cu, Pb, Sn, Zn, Cd, In, Ga, and Se can be recovered under optimal conditions. The optimal conditions for the dissolution of Cu, Zn, and Cd were a glycine concentration of 0.5 M, a temperature of 25 °C, a solid/liquid ratio of 10 gr/L, and 1% of hydrogen peroxide. The optimized glycine concentration for the leaching of lead and tin was 1.5 M. Indium and gallium were recovered at 100% by the use of 5 M hydrochloric acid, S/L ratio = 10 gr/L, and T = 45 °C. Separation of selenium and tellurium occurred using 0.5 M HCl at a temperature of 60 °C. Additionally, for the first time, a general outlook for the recycling of various end-of-life solar panels is suggested.

A step towards RoHS compliance for perovskite devices by using a novel lead-capturing encapsulant

Despite the significant progress made in perovskite solar cells, device degradation under ambient conditions and the potentially hazardous release of toxic lead into the environment is a major concern. Packaging and encapsulation of solar cells and modules will address these issues to an extent. However, during leaching mobile lead ions can diffuse through most commercially used edge seal adhesives, making even standard encapsulation systems not appropriate for packaging perovskite solar cells. In this work, an ionomer of polyethylene co-methacrylic acid polymer film (Surlyn) modified with functional groups that interact with mobile lead ions is used to encapsulate perovskite films. The functionalization of the encapsulant was tailored by modifying the matrix polymer with Zeolitic imidazolium framework- 67 (ZIF-67) through polydopamine as the anchoring platform. This modified encapsulant exhibited a reduced lead leaching by more than ∼8 orders. The design of experiments was carried out to evaluate the modified encapsulant efficacy in preventing lead leaching through it. In addition, new experimental techniques were designed for understanding the characteristics and reliability for an extended period.