Metal Leaching Research Articles

Photo-assisted Fenton degradation of tetracycline hydrochloride with magnetic Fe3S4/CuS composite

In recent years, semiconductor materials have gradually become popular through photodegradation of organic pollutants, and the semiconductor materials Fe3S4 and CuS have their own shortcomings. To make both materials useful, Fe3S4/CuS composites were prepared by hydrothermal method and degradation experiments were carried out using tetracycline hydrochloride (TCH) as a simulated pollutant. The effects of factors such as the mass ratio of Fe3S4 to CuS, temperature, pH changes, the consume of H2O2, and the amount of catalyst added on the degradation of TCH were explored. At room temperature, the Fe3S4/CuS composites exhibit good Fenton degradation efficiency. The F1C1.5 composite (mass ratio of Fe3S4 to CuS is 1:1.5) achieved 74.60 % at pH 4.0 within one hour. Subsequently, the free radical capture experiments and metal leaching experiments were conducted, and it was found that the active substance h+ played a major role. At the same time, the F1C1.5 composite shows stability, allowing for a lower concentration of iron leaching and having high catalytic activity after 5 cycles. These degradation properties, together with the ease of fabrication of the catalyst, will facilitate the practical application of this system in the continuous removal of TCH.

Natural sea water and artificial sea water are not equivalent in plastic leachate contamination studies

Background Plastic contamination is one of the concerns of our age. With more than 150 million tons of plastic floating in the oceans, and a further 8 million tons arriving to the water each year, in recent times the scientific community has been studying the effects these plastics have on sea life both in the field and with experimental approaches. Laboratory based studies have been using both natural sea water and artificial sea water for testing various aspects of plastic contamination, including the study of chemicals leached from the plastic particles to the water. We set out to test this equivalence, looking at the leaching of heavy metals form plastic particles. Methods We obtained leachates of polyvinyl chloride plastic pre-production nurdles both in natural and artificial sea water and determined the elements in excess from untreated water by Inductively coupled plasma – optical emission spectrometry. We then used these different leachates to assess developmental success in the tunicate Ciona intestinalis by treating fertilised eggs through their development to hatched larvae. Results Here we report that chemical analysis of polyvinyl chloride plastic pre-production pellet leachates shows a different composition in natural and artificial sea water. We find that the zinc leaching from the plastic particles is up to five times higher in natural seawater than in artificial seawater, and this can have an effect in the toxicological studies derived. Indeed, we observe different effects in the development of C. intestinalis when using leachates in natural or artificial sea water. We also observe that not all artificial sea waters are suitable for studying the development of the tunicate C. intestinalis. Conclusions Our results show that, at least in this case, both types of water are not equivalent to produce plastic leachaetes and suggest that precaution should be taken when conclusions are derived from results obtained in artificial sea water.

Synthesis of Sm‐TADDbBP@MCM‐41 as a Robust, Reusable, and Practical Nanocatalyst in the Homoselective [2 + 3] Cycloaddition Reaction

ABSTRACTSchiff‐base materials are known ligands for the coordination of metal ions and the synthesis of various stable and useful complexes. Therefore, herein, a novel Schiff‐base compound {2,2′‐((1E,11E)‐2,5,8,11‐tetra azadodeca‐1,11‐diene‐1,12‐diyl) bis (4‐bromophenol)} was introduced that formed from condensation of triethylenetetramine (TETA) and 5‐bromo‐2‐hydroxybenzaldehyde (5B2HB). This Schiff‐base ligand was labeled as TADDbBP. Besides, mesoporous MCM‐41 was synthesized using tetraethyl orthosilicate (TEOS), hydrolyzing cetyltrimethylammonium bromide (CTAB) and NaOH solution (2 M), followed by calcination at 550 °C, and further, the silanol sites on the MCM‐41's surface were modified by 3‐chloropropyltriethoxysilane (3Cl‐PTES), which modified MCM‐41 was labeled as 3‐Cl‐Pr@MCM‐41. In the next step, the synthesized TADDbBP (as Schiff‐base ligand) was grafted on 3‐Cl‐Pr@MCM‐41, which was labeled as TADDbBP@MCM‐41, and further, it was coordinated with samarium ions (which was labeled as Sm‐TADDbBP@MCM‐41 nanocatalyst) using Sm (CH3COO)3. This is the first report on the production of Sm‐TADDbBP@MCM‐41 nanocatalyst, this nanocatalyst was characterized by TEM, SEM, EDX, elemental mapping, BET method, ICP, XRD, and TGA techniques. In the final step, the catalytic performance of Sm‐TADDbBP@MCM‐41 nanocatalyst has been checked in the homo‐selective producing of tetrazoles through [2 + 3] cycloaddition of benzonitriles and sodium azide (NaN3) in PEG‐400 as available, nontoxic, green, and safe solvent. This nanocatalyst provides excellent selectivity in the synthesis of tetrazoles. In addition, Sm‐TADDbBP@MCM‐41 nanocatalyst can be separated and recycled for several cycles without significant reactivation or metal leaching.

Preparation of printing and dyeing sludge biochar/macromolecule polymer microsphere as a non-sacrificial persulfate activator with excellent reusability and reduced heavy metals leaching

Biochar-based environmental functional materials offer a promising approach for the resourceful utilization of printing and dyeing sludge (PADS). However, pollutant desorption and heavy metal leaching pose potential environmental risks. In this study, we developed a novel PADS biochar (PADSBC) macromolecule polymer microsphere with outstanding reusability and stability. This microsphere effectively activated peroxymonosulfate (PMS) for the degradation of sulfadiazine (SDZ) while significantly reducing heavy metal leaching compared with PADSBC. The SDZ removal efficiency was not influenced by the type of macromolecule polymers (calcium alginate (CA), cellulose nanofibers (CNF), and polyvinyl alcohol (PVA)) incorporated into PADSBC. In the CA-PADSBC800 microspheres/PMS system, 97% of SDZ was removed within 40 min, primarily through 1O2-induced oxidative degradation (62%) and adsorption by CA-PADSBC800 (29%). Additionally, CA-PADSBC800 prevented SDZ desorption for over five consecutive cycles, while PADSBC800 exhibited 25% desorption. The presence of HCO3- and humic acids slightly delayed SDZ removal, while Cl- slightly accelerated it. Doping CA, CNF, and CA+CNF into PADSBC800 reduced the leaching of Cu and Cr by over 90%, and Ni by over 80%, under both experimental conditions and simulated surface water and landfill leachate situations. The excellent performance of the PADSBC-macromolecule polymer microspheres was attributed to the presence of carboxyl, hydroxyl, and C=O functional groups.

Enhanced geopolymerization of MSWI fly ash through combined activator pretreatment: A sustainable approach to heavy metal encapsulation and resource recovery

With the rapid pace of socioeconomic progress, there has been a continuous rise in the generation of municipal solid waste incineration (MSWI) fly ash. Enhancing the efficiency of MSWI fly ash utilization, minimizing expenses, and developing more cost-effective and environmentally sustainable cementitious materials represent critical scientific challenges that warrant immediate attention. The research commenced with the preliminary treatment of MSWI fly ash using a blend of chemical activators and a water rinsing method. Following this, quicklime and coal fly ash were incorporated to formulate a geopolymer derived from MSWI, aimed at stabilizing the MSWI fly ash. Throughout this investigation, a selection of five chemical activators—calcium hydroxide, sodium hydroxide, sodium silicate, dilute sulfuric acid, and citric acid—was employed in conjunction with a water-washing procedure to condition the MSWI fly ash. Three single factor experiments denoted A, B, and C, were designed, and the corresponding geopolymer samples were prepared. In this research, the analysis focused on the solidified MSWI fly ash-based geopolymer samples, examining their physical and chemical characteristics, compressive strength, levels of heavy metal release, and the structure at a microscopic level. The findings revealed that the B3 series exhibited the most substantial 28-day compressive strength, reaching 1.692 MPa. Concurrently, the concentrations of leached heavy metals, including zinc (Zn), copper (Cu), chromium (Cr), lead (Pb), cadmium (Cd), and nickel (Ni), were all beneath the regulatory thresholds stipulated by the GB16889 and GB18598 criteria, signifying a notably effective solidification outcome. During the geopolymerization process, gel phases such as calcium aluminosilicate hydrate (C-A-S-H) and calcium silicate hydrate (C-S-H) are formed within the geopolymer matrix. This leads to the formation of a compact and cohesive cementitious material, which showcases superior mechanical strength and a robust capacity for heavy metal sequestration. This research contributes to the safe management of MSWI fly ash by not only facilitating its non-hazardous disposal but also enabling the efficient containment and elimination of heavy metals, chloride ions, and elemental aluminum.

Biostabilization of fecal sludge and tannery liming sludge: A novel approach

Fecal sludge and tannery liming sludge management is essential for humans and the environment. The emitted amount of waste from two industries is reduced in composting leading to value-added products. This research focused on the effectiveness and feasibility of co-composting fecal sludge and hair-burning liming sludge from tannery. Fecal sludge was intermittently mixed with hair-burning liming sludge which also consisted of chicken manure and sawdust. Five piles (Pile 1, Pile 2, Pil3, Pile 4, and Pile 5) indicated respectively as P#1, P#2, P#3, P#4, and P#5, contained various ratios of composting materials were mixed, piled onto a horizontal bamboo frame, and observed for 120 days. To ensure a suitable oxygen supply, the composting piles were turned on in the thermophilic stage so that pathogens could not survive. The highest temperatures in the thermophilic stage were 39.0°C, 49.2°C, 55.7°C, 41.7°C, and 51.3°C. These referred to the respective piles P#1, P#2, P#3, P#4, and P#5. The Dewar stability index confirmed the stability of each composting pile, and the maximum degradation was found for P#3. The metals chromium (Cr), zinc (Zn), lead (Pb), iron (Fe), and nickel (Ni) in the final compost were found to be 38.1, 144.7, 15.1, 450.5, and 22.7 mg/kg, respectively. TCLP results reveal only an insignificant amount of metal leaching. Fecal coliform of the compost was below the standard level; Helminth eggs and Salmonella spp. were absent. SEM micrographs reflect the decomposition of composting materials. The maximum germination index and germination capacity of compost pile P#3 for compost-soil ratio 1:0 and 1:1 were 90%-92.8% and 100%, respectively. The present approach produced nutrient-enriched compost from fecal sludge and hair-burning liming sludge from a tannery emerges as a suitable solution for reducing solid wastes.

Enhancing the interface stability of Li/NCM622 batteries by adding 3-trifluoromethyl pyrazole

In this study, 3-trifluoromethylpyrazole (TMPZ) was developed as a multifunctional electrolyte additive to enhance wettability between separator and electrolyte, CEI formation and remove HF to improve the performance of Li/NCM622 batteries by experiment and theoretical calculation. After 200 cycles at 30 °C, the discharge capacity retention of batteries at 1 C with 0.5 wt% TMPZ additive is remarkably enhanced from 68.3 % to 83.2 %. The enhanced electrochemical performance of the batteries by adding TMPZ additive is evaluated by the spectroscopic characterization and theoretical calculation. It is demonstrated that TMPZ can generate uniform and dense CEI film via ring-opening electrochemical polymerization of TMPZ on the NCM622 electrode surface. The CEI film helps to suppress the breakdown of LiPF6 electrolyte and the leaching of transition metals, effectively avoiding harmful side reactions between the NCM622 electrode and the electrolyte. Furthermore, introducing TMPZ can enhance the wettability between separator and electrolyte, therefore providing more channels of Li+ to accelerate reaction kinetics of batteries.

Insights into the environmental risk variation of heavy metals from MSWI fly ash after thermal plasma vitrification

Thermal plasma vitrification of municipal solid waste incineration fly ash (MSWI FA) shows potential for effective dioxin degradation and heavy metal immobilization. However, the environmental risks posed by heavy metals released after vitrification remain understudied. This work investigates two types of MSWI FA—circulated fluidized bed fly ash (CFA) and mechanical grate furnace fly ash (GFA)—blended with waste glass and vitrified via thermal plasma treatment. The physical and chemical properties of the original FA and vitrified glasses (CFA-glass and GFA-glass) were analyzed. Environmental risks were assessed using the risk assessment code (RAC) and the overall pollution toxicity index (OPTI). Results showed that CFA, with higher Si and Al content, exhibited better vitrification than GFA. Plasma vitrification reduced chlorine content from 5.79 % and 10.59 % to 0.22 % and 0.16% due to Cl volatilization. Heavy metals with low boiling points, such as Cd and Pb, were significantly reduced, while high-boiling-point Cr, Ni remained and the acid resistance of vitrificated FA significantly deteriorated, which increased the potential leaching of heavy metals. In alkaline conditions, the OPTI value of CFA-glass dropped to 2, indicating a strong immobilization effect. This study provides critical insights for managing heavy metals in fly ash through thermal plasma vitrification.

Exploring the Mechanisms and Kinetic Modeling of Phenol Amination Using Pd and Rh‐Based Catalysts

AbstractProducing biomass‐derived chemicals to substitute their petrochemical counterparts has long been an aspiration of the green chemistry research community. However, synthesizing secondary amines from biomass precursors presents several challenges related to catalyst nature and the mechanistic understanding of reaction systems. Here, we unravel the mechanistic and kinetic implications of the reductive amination of phenol with cyclohexylamine over Pd/C and Rh/C. A competitive Langmuir‐Hinshelwood reaction model well interpreted the kinetic data, suggesting that support‐metal interfaces serve as active sites for H2, ─NH2 and ═NH activation. The apparent activation energies for imine hydrogenation were 87.6 kJ mol−1 (Pd/C) and 34.5 kJ mol−1 (Rh/C), while ΔHads and ΔSads values confirmed the physicochemical consistency of the model. Moreover, the catalysts demonstrated their high stability to operate for several catalytic cycles, with minor activity losses due to metal leaching and partial sintering of Pd nanoparticles. Despite phenol reductive amination following similar mechanisms on Rh/C and Pd/C, they show differences in selectivity because the hydrogenation of imine is more efficient on Rh0 than on Pd0. This is the first mechanism‐oriented kinetic study for phenol reductive amination; thus, it provides valuable information for process design and scale‐up.

Enhanced selective oxidation of ethylarenes using iron single atom catalysts embedded in Nitrogen-Rich graphene

Heavily (19 % wt) Nitrogen doped graphene (N-G), with Nitrogen incorporated mainly as pyridinic species (77.8 %), was obtained by reacting fluorographene with ammonia under solvothermal conditions, at mild temperature (140 °C). N-G was used to stabilize single iron atoms (N-G-Fe) in two different configurations: low spin X-(FeIIN4)-Y and high spin X-(FeIIIN4)-Y. The resulting N-G-Fe single atom catalysts exhibit remarkable efficacy in the selective oxidation of ethylarenes, with activity comparable or even superior to state-of-the-art materials, converting ethylbenzene to acetophenone with an initial turnover frequency of 13400 h−1. Notably, N-G-Fe exhibits genuine catalytic activity since it is able to oxidize ethylbenzene using substoichiometric amount of peroxides, and exploiting molecular oxygen as the final oxidant. Moreover, N-G-Fe can be recycled without any metal leaching, and exhibits a broad catalytic scope. Multi-technique characterizations combined with rationally designed catalytic tests allowed us to identify the active sites and propose a plausible mechanism for the catalytic cycle.

Recovery of Magnetic Ni Particles from Spent Catalyst Leachate by Direct Cementation

An alternative method based on cementation for the recovery of nickel from spent Ni/Al2O3 reforming catalyst pregnant leach solution (PLS) was proposed to overcome the limitations of traditional two-step extraction and precipitation processes. Thermodynamic analysis was used to evaluate the potential interference of key reactions, such as nickel and sacrificial metal leaching, with the selective cementation of nickel from the PLS. Key variables in the cementation process were optimized using response surface methodology (RSM) combined with Box–Behnken design (BBD). Under optimal conditions—pH 2.2 ± 0.1, processing time of 15 min, and Al/Ni molar ratio of 2.65—a maximum nickel recovery of 73.2% was achieved. Extensive characterization confirmed the high quality of the cemented nickel product: (i) ICP-OES indicated nickel purity of 99.47%, (ii) XRD patterns verified the presence of pure face-centered cubic nickel, (iii) SEM-EDS and vibrating sample magnetometry confirmed the high purity of the metallic nickel particles.

ZIFs@MIL-101/urea-derived magnetic FeCo nitrogen-rich carbon as an effective and stable catalyst for peroxymonosulfate activation

High efficiency and stability are key issues in heterogeneous metal catalytic materials/peroxymonosulfate (PMS) systems during wastewater degradation. However, catalytic materials that are difficult to recover and metal leaching can cause secondary contamination of water bodies. Herein, we designed the magnetic FeCo nitrogen-rich carbon (FeCo-NC) obtained by layer-by-layer encapsulation, followed by urea encapsulation of in situ grown MOF-in-MOF and carbonization. The CoFe2O4 crystalline nature of FeCo-NC was confirmed by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and selected angle electron diffraction (SAED) results, which is responsible for the magnetic properties of FeCo-NC. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) present that the material's morphology transforms from dodecahedral ZIF-67 to spindle-shaped ZIF-67@MIL-101 and then to octahedral FeCo-NC. Compared with FeCo-C and ZIF-67@MIL-101, the removal efficiency of FeCo-NC was maintained at 78.6 % after 10 consecutive cycles, with only a 17 % loss of raw material. The Fe and Co leaching amounts in the FeCo-NC/PMS system were approximately 0.6 and 0.1 mg/L, respectively, much lower than China's Fe and Co emission standards. FeCo-NC characterization and TC degradation results demonstrated that magnetic CoFe2O4 nanoparticles formed on the surface or inside the FeCo-NC could effectively inhibit metal (Fe and Co) loss and be easily regenerated in multiple degradation cycles. The mechanism and degradation routes in the FeCo-NC/PMS/ TC system, including the radical/nonradical pathways, Fe/Co valence change, and electron transfer, were further investigated by electron paramagnetic resonance experiments, electrochemical analyses, in situ Raman spectroscopy, and HPLC–MS experiments.

Influence of earthworms on the mobility and bioavailability of metals, metalloids and radionuclides in historically contaminated soil

While soil characteristics such as pH, cation exchange capacity and organic matter are known to influence the mobility of pollutants in soil and the transfer to vegetation, far less attention has been paid to the possible non-trophic influence of organisms on pollutant transfer to other species. When pollutants are present in a bound unavailable form in the mineral or organic fraction, they can be made available through bio-weathering and decomposition of organic material. Within this study, the impact of earthworms on the mobility of metal(loid)s and radionuclides in soil and their transfer to vegetation was evaluated and the pathways through which earthworms work were studied. Soil from a Belgian field, historically contaminated with metal(loid)s and radionuclides, was used and microcosm systems were applied to mimic the natural interactions between soil, earthworms (Lumbricus terrestris) and vegetation (Lolium perenne). Metal and radionuclide concentrations were determined in soil, pore water and grass. In addition, soil pH, (chromophoric) dissolved organic matter, the ionic composition of pore water and the soil microbial activity were analysed. In general, earthworm presence significantly increased the concentration of most pollutants in soil pore water. This could be a direct consequence of decreased soil pH and increased humification. The latter also lead to higher nutrient concentrations in pore water that were depleted in the root zone due to high accumulation by plants. Indications were found for earthworm-induced effects on the soil microbial activity. The results show that earthworm activity can increase leaching of metal(loid)s and radionuclides and enhance dispersion into the environment and transfer to other biota and the food chain. Biologically induced release or remobilization of pollutants in the soil should therefore be considered in the context of risk assessment and site management strategies.

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.

Stabilization of clay soil using alkali-activated sewage sludge

This study investigates the innovative reuse of sewage sludge with eco-friendly alkaline solutes to improve clayey soil without conventional cementitious binders. The unconfined compressive strength (UCS) was the main criterion to assess the quality and effectiveness of the proposed solutions, as this test was performed to measure the strength of the stabilized clay by varying binders’ dosages and curing times. Moreover, the direct shear test (DST) was used to investigate the Mohr-Coulomb parameters of the treated soil. Microstructure observations of the natural and treated soil were conducted using scanning electron microscope (SEM), energy-dispersive spectroscopy (EDS), and FTIR. Furthermore, toxicity characteristic leaching procedure (TCLP) tests were performed on the treated soil to investigate the leachability of metals. According to the results, using 2.5% of sewage sludge activated by NaOH and Na2SiO3 increases the UCS values from 176 kPa to 1.46 MPa after 7 d and 56 d of curing, respectively. The results of the DST indicate that sewage sludge as a precursor increases cohesion and enhances frictional resistance, thereby improving the Mohr-Coulomb parameters of the stabilized soil. The SEM micrographs show that alkali-activated sewage sludge increases the integrity and reduces the cavity volumes in the stabilized soil. Moreover, TCLP tests revealed that the solubility of metals in the treated soil alkali-activated by sewage sludge significantly decreased. This study suggests that using sewage sludge can replace cement and lime in ground improvement, improve the circular economy, and reduce the carbon footprint of construction projects.

Increasing the Efficiency of Underground Block Leaching of Metal

The purpose of this study is to increase the efficiency of underground block metal leaching by increasing the metal content in the pregnant solution using the cavitation effect. To achieve this goal, it is proposed to process (cavitate) the leaching solution on the injector. The following research methods were used in this study: analysis of the current state of scientific and technical problems and research, laboratory work to establish the effect of the treated (cavitated) solution on the metal content in the pregnant solution, collection and processing of statistical data from laboratory work, analysis of research results, and preparation of conclusions. According to the results of laboratory research, leaching with a treated solution on an injector leads to an increase in the content of a useful component in the pregnant solution. The maximum increase in the metal content in the pregnant solution was achieved by processing the leaching solution for 5 min. The effectiveness of the solution over time after treatment was maintained for a long time (up to one month). Changes in the solution pressure did not affect the effectiveness of the treated leaching solution. The scientific novelty of this work consists of determining the dependence of the content of the useful component in the pregnant solution on the time of processing the leaching solution on the injector and the leaching time, which determines the optimal time for processing the solution on the injector to obtain the maximum metal content in the pregnant solution. The dependence of the content of the useful component in the solution on the pressure during leaching with untreated and treated solutions on the injector was obtained. Doi: 10.28991/CEJ-2024-010-10-014 Full Text: PDF

Synergistic effect of rhamnolipid and Bacillus mucilaginosus on detoxification and activation of municipal solid waste incineration fly ash

In recent years, the substantial increase in municipal solid waste incineration fly ash (MSWIFA) production has made its treatment a critical issue. However, the high toxicity of MSWIFA makes its utilization still in the exploratory stage. In this study, the heavy metal leaching rate, particle size distribution and activity index of MSWIFA were tested to investigate the detoxification and activation effects of Bacillus mucilaginosus on MSWIFA by introducing rhamnolipid. The results show that the microbial treatment can greatly increase the leaching rate of heavy metals in MSWIFA and its 28-day and 90-day activity indexes, especially by the synergistic treatment. For the Bacillus mucilaginosus and rhamnolipid treated MSWIFA (BR-MSWIFA), the maximum leaching rates follow the order from high to low of 85.57% Cr, 78% Cu, 76.38% Zn, 62.78% Pb and 37.65% Mn, while having a low mass loss of less than 5%, which is important for its reuse. Moreover, compared with the untreated MSWIFA (U-MSWIFA), the average particle sizes of Bacillus mucilaginosus treated MSWIFA (B-MSWIFA) and BR-MSWIFA decrease from 8.39 μm to 7.80 μm and 4.31 μm, and the 28-day activity indexes increase from 80.19% to 101.59% and 110.61%. The effect mechanism is that rhamnolipid not only can promote the growth, reproduction, and metabolic acid production of Bacillus mucilaginosus, but also disperse the extracellular polymeric substance (EPS) and MSWIFA particles, thus increase their contact area and the bioleaching. This study provided a theoretical foundation for the harmless treatment and resource utilization of solid wastes containing heavy metals.

Molybdenum doping leads to faster photo-dissolution of commercial molybdate red pigment than chrome yellow pigment under sunlight irradiation

The photo-dissolution of lead chromate pigments poses specific environmental hazards. In this study, we report that doping molybdenum in lead chromate pigments, resulting in commonly known molybdate red pigment, increases the risk of heavy metal leaching when exposed to light. Commercial molybdate red pigments undergo photo-dissolution when exposed to simulated sunlight and exhibit lower photostability compared to lead chromate pigments such as chrome yellow. After 24 h of irradiation, the leaching rates of toxic lead and chromium from molybdate red pigments were 2.98 and 3.70 times higher, respectively, than those from chrome yellow pigments. The primary factor leading to decreased pigment photostability is the activation of pigment semiconductors facilitated by molybdenum doping. Molybdate red pigments exhibit a broader light absorption spectrum and more efficient separation and transfer of photogenerated charge carriers than chrome yellow pigments, boosting the photochemical activity. To the best of our knowledge, this is the first study to illustrate the doping effect on the photostability of commercial inorganic pigments and the consequent heavy metal leaching. Our results suggest that Mo doping reduces the photostability of lead chromate pigments, highlighting the potential elevated environmental risks associated with complex inorganic pigments.

Development and Validation of an ICP‐OES Method to Determine Extractable and Leachable Metals in HDPE (Plastic) Pharmaceutical Packaging Material

ABSTRACTThe safety and effectiveness of pharmaceutical medicines depend heavily on extractables and leachables. Patients may be adversely affected by contaminants that enter drug products through packing materials. As a result, regulatory organizations like the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have set standards and regulations for evaluating and managing extractables and leachables. Characterizing the packing materials, carrying out extraction experiments and checking the extracted solutions for contaminants are all parts of this research. As part of the process for approving new drugs, regulatory agencies make use of these data. In present work, an inductively coupled plasma optical emission spectroscopy (ICP‐OES) method is developed and validated for quantifying trace elements from a high‐density polyethylene (HDPE) packaging material. The approach delineated in accordance with United States Pharmacopoeia (USP) <661.1> and <661.2> for the comprehensive analysis of 16 metallic elements including aluminium, arsenic, cadmium, chromium, cobalt, lead, mercury, nickel, titanium, vanadium, zinc, zirconium, barium, manganese, calcium and tin is applicable for evaluating the efficacy of packaging materials. The method detection limits (MDLs) complied as per USP 39‐NF 34 <661.1> along with relative standard deviations (RSDs) obtained were ranging from 0.3% to 3.1% and recoveries of all elements spiked at two different trace levels in HDPE samples were within 97%–110%, providing sensitive, accurate and reproducible methodology.

Utilisation of acid-tolerant bacteria for base metal recovery under strongly acidic conditions.

Hydrometallurgical bioprocesses for base metal recovery in environmentally friendly electronic device waste (e-waste) recycling are typically studied under neutral pH conditions to avoid competition between metals and hydrogen ions. However, metal leachate is generally strongly acidic, thus necessitating a neutralisation process in the application of these bioprocesses to e-waste recycling. To solve this pH disparity, we focused on acid-tolerant bacteria for metal recovery under strongly acidic conditions. Four acid-tolerant bacterial strains were isolated from neutral pH environments to recover base metals from simulated waste metal leachate (pH 1.5, containing 100 or 1000 mg L-1 of Co, Cu, Li, Mn, and Ni) without neutralisation. The laboratory setting for sequential metal recovery was established using these strains and a reported metal-adsorbing bacterium, Micrococcus luteus JCM1464. The metal species were successfully recovered from 100 mg L-1 metal mixtures at the following rates: Co (8.95%), Cu (21.23%), Li (5.49%), Mn (13.18%), and Ni (9.91%). From 1000 mg L-1 metal mixtures, Co (7.23%), Cu (6.82%), Li (5.85%), Mn (7.64%), and Ni (7.52%) were recovered. These results indicated the amenability of acid-tolerant bacteria to environmentally friendly base metal recycling, contributing to the development of novel industrial application of the beneficial but unutilised bioresource comprising acid-tolerant bacteria.