Sources Of Metals Research Articles

Mineralogy and Geochemistry of High-Sulfur Coals from the M8 Coal Seam, Shihao Mine, Songzao Coalfield, Chongqing, Southwestern China

Mineral matter, including minerals and non-mineral elements, in coal is of great significance for geological evolution, high-value coal utilization, and environment protection. The minerals and elemental geochemistry of Late Permian coals from the M8 coal seam, Shihao mine, Songzao coalfield in Chongqing, were analyzed to evaluate the sediment source, sedimentary environment, hydrothermal fluids, and utilization prospects of critical metals. The average total sulfur (4.21%) was high in coals, which mainly exists in the forms of pyritic sulfur. Kaolinite, pyrite, calcite, quartz, illite and illite/smectite (I/S) mixed layers, and anatase predominated in coals, with trace amounts of chlorite, ankerite, and siderite. Epigenetic cell- and fracture-filling pyrite, veined calcite, and ankerite were related to hydrothermal fluids and/or pore water after the diagenesis stage. Compared to the world’s hard coals, As and Cd are enriched in the Shihao M8 coals, and Li, Cr, Co, Zr, Mo, Pb, and Tb are slightly enriched. These high contents of sulfophile elements may be related to seawater intrusion. The terrigenous clastics of the Shihao M8 coals originated from the felsic–intermediate rocks atop the Emeishan Large Igneous Provinces (ELIP) (Kangdian Upland), while the roof and floor samples were derived from Emeishan high-Ti basalt. Through the combination of sulfur contents and indicator parameters of Fe2O3 + CaO + MgO/SiO2 + Al2O3, Sr/Ba and Y/Ho, the depositional environment of peat swamp was found to be influenced by seawater. Although the critical elements in coal or coal ash did not reach the cut-off grade for beneficial recovery, the concentration of Li and Zr were high enough in coal ash.

Resource utilization of field acid mine drainage: Formation of layered double hydroxides, its removal capacity and mechanism for antimony

Although acid mine drainage (AMD) has been recognized as a major environmental pollutant, it is also a potential source of valuable metals and sulfate. In this study, a resource utilization approach of field AMD for the formation of iron-based layered double hydroxides (LDHs) with sulfate intercalation was proposed and its capacity for removing antimonate [Sb(V)] was examined. Layered double hydroxides derived from field AMD possesses a more rapid equilibration time (<120 min) and a larger removal capacity (78 mg g−1) for Sb(V) compared with other LDHs from chemical reagents. Following the treatment of field AMD containing 10.7 mg L−1 Sb, a residual Sb concentration of 4.0 μg L−1 was achieved using a dose of 1 g L−1 LDHs, which meets the drinking water standard of 5 μg L−1 recommended by China's Ministry of Health. Leaching tests showed negligible metal(loid)s dissolution in Sb-loaded LDHs over a short period. The interactions between Sb(V) and LDHs include anion exchange and formation of brandholzite, which were further investigated at the electronic scale using density functional theory (DFT) calculations. It is envisaged that this approach for preparing LDHs will provide theoretical support for the remediation and resource recovery of AMD.

Impacts of atmospheric deposition on the heavy metal mobilization and bioavailability in soils amended by lime

Atmospheric deposition is an important source of heavy metal in agricultural soils, but there is limited research on the mobility of these metals in soil and their impact on soil amendment. Here, we performed a dust incubation experiment in soils in the laboratory and a factorial transplant experiment at three field sites with a gradient of atmospheric deposition to examine the impacts of atmospherically deposited heavy metals (Cu, Cd, and Pb) on the mobility and bioavailability in soils with and without lime applications. Results showed that the atmospherically deposited heavy metals showed high mobility and were primarily presented in the soluble ionic fractions in the wet part and acid-exchangeable and reducible fractions in the dry part of atmospheric deposition. Atmospheric dust addition caused the 2p3/2 and 2p1/2 electrons of Cu atoms in uncontaminated soils to transition the 3d vacant states, resulting in similar copper absorption peaks as atmospheric particles by the observation of X-ray absorption near-edge spectroscopy (XANES). In the field, atmospheric deposition can only increase the mobile fractions in the surface soils, but not in the deeper layers. However, the deposition can increase the soluble and diffusive gradients in thin films (DGT)-measured bioavailable fractions in profile along with the soil depth. Lime applications cannot significantly reduce the mobile fractions of heavy metals in the surface soils exposed to atmospheric deposition, but significantly reduce the heavy metal concentrations in soil solutions and the DGT-measured bioavailable concentrations, particularly in the deeper layer (6–10 cm). The major implication is that atmospherically deposited heavy metals can significantly increase their bioavailable concentrations in the plough horizon of soil and constrain the effects of soil amendments on heavy metal immobilization, thereby increasing the risks of crop uptake.

Heavy Metals in Agricultural Soils: Sources, Influencing Factors, and Remediation Strategies.

Soil heavy metal pollution is a global environmental challenge, posing significant threats to eco-environment, agricultural development, and human health. In recent years, advanced and effective remediation strategies for heavy metal-contaminated soils have developed rapidly, and a systematical summarization of this progress is important. In this review paper, first, the anthropogenic sources of heavy metals in agricultural soils, including atmospheric deposition, animal manure, mineral fertilizers, and pesticides, are summarized. Second, the accumulation of heavy metals in crops as influenced by the plant characteristics and soil factors is analyzed. Then, the reducing strategies, including low-metal cultivar selection/breeding, physiological blocking, water management, and soil amendment are evaluated. Finally, the phytoremediation in terms of remediation efficiency and applicability is discussed. Therefore, this review provides helpful guidance for better selection and development of the control/remediation technologies for heavy metal-contaminated agricultural soils.

Source apportionment of soil heavy metals based on multivariate statistical analysis and the PMF model: A case study of the Nanyang Basin, China

Analyzing the spatial variation characteristics of heavy metals in soil and identifying their sources is crucial for preventing, controlling, and managing regional environmental pollution. In this study, 5778 surface soil samples were collected from the Nanyang Basin. The content characteristics of five heavy metals (As, Cr, Cd, Hg, and Pb) were determined and analyzed. The spatial distribution characteristics of these heavy metals in the soil were investigated using inverse distance interpolation and spatial autocorrelation analysis. Additionally, the sources of heavy metals in the soil were qualitatively and quantitatively explored through PCA and PMF models. The results revealed that the mean values of all elements, except As and Hg, exceeded the country soil background values. Spatially, the distribution of soil heavy metal elements showed evident heterogeneity and autocorrelation, with obvious differences between the western and eastern regions, where heavy metal concentrations were generally higher in the west and lower in the east. Four sources of heavy metals were identified in the study area: mining sources, natural sources, transportation sources, and a combined source of atmospheric deposition and agricultural activities. The element As was primarily derived from natural sources (80.90%). The element Cr was influenced by multiple factors, mainly from mining sources (66.20%) and natural sources (31.80%). Transportation sources (46.30%) and mining sources (44.80%) were the primary influences on the element Cd. The element Pb was influenced by transportation sources (64.70%) and natural sources (18.11%). The element Hg was mainly influenced by both atmospheric deposition from coal combustion and agricultural activities (90.50%).

Characterization of soil trace metal pollution, source identification, and health risk assessment in the middle reaches of the Guihe River Basin.

The natural environment, as well as human production and survival, is intrinsically dependent on soil. This study comprehensively assessed the pollution status, health risks, and sources of trace metals in the middle reaches of the River Gui Basin (MRGB) utilizing the geoaccumulation index, potential ecological risk index (PERI), and human health risk evaluation method. The findings of this study provide the following key insights: (1) only Cu and Pb levels in the MRGB soils did not exceed the background values established for soils in Weifang City (WFC). (2) The geoaccumulation status in most areas of the MRGB ranged from non-polluted to mildly polluted, with the overall ecological risk classification ranging from mild to moderate. (3) The cumulative non-carcinogenic risk for humans in the MRGB remained within acceptable limits, whereas the carcinogenic risk indices fell within tolerable levels. Oral ingestion emerged as the primary exposure pathway for both non-carcinogenic and carcinogenic health risks. (4) Cu, Zn, Ni, and Cr concentrations in MRGB soils primarily stemmed from natural sources associated with parent rocks, with Zn exhibiting additional influence from anthropogenic factors. In contrast, Pb, Cd, Hg, and As concentrations were predominantly driven by anthropogenic sources. Although the soils in the MRGB typically exhibited mild-to-moderate contamination levels, the contamination levels of Hg and Cd were notably more severe. As and Cr were significant health hazards. Most soil contamination sources are attributed to anthropogenic factors, warranting heightened attention from the relevant authorities.

Appraisal of trace metals toxicity and human health risk using a novel approach in wastewater of four gas fields, Bangladesh

The objective of this study is to assess the toxicity of trace metals (TMs) and associated environmental, ecological and health risks in the gas fields located in the Sylhet region of Bangladesh. Gas well-produced water, gas field discharge water, and drinking water surrounding the gas fields were collected for analysis. This study analyzed carcinogenic and noncarcinogenic TMs such as Cr, As, Co, Cd, Fe, Ni, Mn, Zn, and Pb, as well as physical parameters pH and EC in the collected samples using various instruments. The TMs were measured using Atomic Absorption Spectrometer (AAS), Flame AAS and physical parameters were evaluated using portable water multiparameter. The Fe and EC concentrations in produced and discharged water samples were incredibly high. The average concentrations of TMs in produced water samples during the summer and rainy seasons were found to be Fe > Mn > Zn > Ni > Co > Cu > Cr > Pb > As > Cd. The observed metal concentration in discharge water was higher during the summer than in the rainy season. Most samples met national and international standards for trace elements, while a few samples exceeded the threshold value.The Heavy Metal Evaluation Index (HMEI) results indicate that most produced water is highly polluted, while discharge and drinking water are moderate to lightly polluted. The Environmental Pollution Index (EPI) indicates environmental pollution for some produced water samples, while it indicates a moderate to low risk for discharge and drinking water samples. The source of trace metals (TMs) was determined using positive matrix factorization. However, all water samples have an ecological risk index of less than 150, indicating lower risk. Furthermore, the Heavy Metals Toxicity Load (HMTL) was below the allowable toxicity load for all water samples, indicating minimal contamination in the studied water. The non-cancer hazard score (HI) of the studied HMs is more significant for children and females than males. The cancer risk from Ni is a concern, while the cancer risk from Cd and Cr is also a matter of concern. In the end, policymakers can utilize this study's findings to monitor, and control produced water contamination.

The leaching behavior of heavy metal from contaminated mining soil: The effect of rainfall conditions and the impact on surrounding agricultural lands

Contaminated mining soils could lead to heavy metal pollution of surrounding farmlands under rainfall conditions. With the aids of sequential extraction, batch leaching, and dynamic leaching experiments, this study was carried out to investigate the characteristics of heavy metals in contaminated mining soils, understand their leaching behavior under different rainfall conditions, and evaluate the potential effects on surrounding farmlands. The results indicated that the concentrations of heavy metals (Cr, Ni, Cu, Zn, As, Cd, and Pb) in the contaminated mining soils were several or even twenty times higher than their corresponding background values, and Cd, Zn, Cu and Pb had considerable proportions (>50 %) in mobile forms. The leaching amounts of heavy metals from the contaminated mining soils had positive correlation with their contents in acid soluble form, and showed strong dependence on rainfall pH conditions. Acid rainfalls (pH = 4.32) can greatly increase the average annual release of Cd, Zn, Cu and Pb from mine soils in the study area, with increments ranging from 72.4 % (Pb) to 85.9 % (Cd) compared to those under alkaline conditions (pH = 7.42). The leaching of heavy metals was well fitted by two-constant, pseudo second-order and parabolic equations, indicating that their multi-layer sorption/desorption behavior on soil surface was dominated by chemical processes and their release was controlled by the diffusion within the soil pore channels. The two-column leaching experiment showed that the metal-rich leachate can lead to obvious increments of heavy metals in non-residual fractions (in particular Cd in acid soluble form) in surrounding farmlands, which would significantly raise the potential ecological risk associated with heavy metals. These findings indicate the importance of contaminated mining soils as a long-term source of heavy metals and the needs for mitigating the releases of toxic elements, especially in areas with heavy acid precipitation.

Trace metals and pesticides in water-sediment and associated pollution load indicators of Netravathi-Gurupur estuary, India: Implications on coastal pollution

Various environmental indicators were used to evaluate the water and sediment quality of the Netravathi-Gurupur estuary, India, for trace metals and pesticide pollution. The descended order of studied metal concentrations (μg/L) in the water was Fe (592.71) > Mn (98.35) > Zn (54.69) > Cu (6.64) > Cd (3.24) > Pb (2.38) > Cr (0.82) and in sediment (mg/kg) was Fe (11,396.53) > Mn (100.61) > Cr (75.41) > Zn (20.04) > Cu (12.77) > Pb (3.46) > Cd (0.02). However, pesticide residues were not detected in this estuarine environment. The various metal indexes categorised the water as uncontaminated, whereas contamination factor, enrichment factor, geo-accumulation index, degree of contamination and pollution load index indicated low to moderate sediment contamination. Multivariate statistics showed that the dominance of natural sources of trace metals with little anthropogenic impact. Improvement in water/sediment quality during the study period might be due to COVID-19 imposed lockdown.

Post-Collisional Tectonomagmatic Evolution, Crustal Reworking and Ore Genesis along a Section of the Southern Variscan Belt: The Variscan Mineral System of Sardinia (Italy)

Since the early Paleozoic, numerous metallogenic events produced in the Sardinian massif a singular concentration of mineral deposits of various kinds. Among them, the Variscan metallogenic peak represents a late Paleozoic phase of diffuse ore formation linked to the tectonomagmatic evolution of the Variscan chain. Two main classes of ores may primarily be attributed to this peak: (1) mesothermal orogenic-type As-Au ± W ± Sb ores, only found in E Sardinia, and (2) intrusion-related Sn-W-Mo-F and base metals-bearing ores found in the whole Sardinian Batholith, but mainly occurring in central–south Sardinia. Both deposit classes formed diachronously during the Variscan post-compressional extension. The orogenic-type ores are related to regional-scale flows of mineralizing fluids, and the intrusion-related ores occur around fertile intrusions of different granite suites. Metallogenic reconstructions suggest almost entirely crustal processes of mineralization without a significant contribution from the mantle. We summarized these processes with a holistic approach and conceptualized the Sardinian Variscan Mineral System (SVMS), a crustal-scale physical system of ore mineralization in the Sardinian basement. The SVMS required suitable metal sources in the crust and diffuse crustal reworking triggered by heat that allowed (a) the redistribution of the original metal budget of the crust in magmas by partial melting and (b) the production of metal-bearing fluids by metamorphic dehydration. Heat transfer in the Sardinian Variscan crust involved shear heating in lithospheric shear zones and the role of mantle uplift as a thermal engine in an extensional tectonic setting. Lithospheric shear zones acted as effective pathways in focusing fluid flow through a large-scale plumbing system into regional-scale structural traps for ores. Pre-Variscan metal sources of metallogenic relevance may have been (1) the magmatic arc and magmatic arc-derived materials of Ordovician age, extensively documented in E Sardinia crust, and (2) an inferred Precambrian crystalline basement lying under the Phanerozoic crustal section, whose presence has been assumed from geophysical data and from petrological and geochemical characteristics of granite suites. At shallower crustal levels, important contributions of metals may have come from pre-Variscan ore sources, such as the Pb-Zn MVT Cambrian ores of SW Sardinia or the REE-bearing Upper Ordovician paleoplacers of E Sardinia.

Hybrid bimetallic phosphonates as cathode materials for miniaturized in-plane asymmetric supercapacitor device

The utilization of wearable electronic devices facilitates the development of smart and flexible technology as a superior energy storage device that minimizes the dimension of wearable devices. The simple vacuum filtration method was employed to fabricate the micro-supercapacitor device (MSC) using the as-synthesized bimetallic nickel cobalt phosphonate (NiCoNPO) on the PVDF membrane as substrate. Novel microporous bimetallic metal phosphonates (NiCoNPO, Ni2CoNPO, NiCo2NPO) have been synthesized in a hydrothermal reaction condition by varying the molar ratio (Ni1:Co1; Ni2:Co1; Ni1:Co2) of metal sources without any employment of templating agent. Among these, NiCoNPO exhibits the remarkable specific capacitance of 2308 F g−1 at 1 mV s−1 and long-term cyclic stability up to the 5000th cycle with 99.6 % capacity retention in the three-electrode system. In addition, the electrode material demonstrates an exceptional capacitance of 574 F g−1 with stability (87.6 % retention) in a two-electrode system. Also, it displays excellent performance as a flexible MSC device with an areal capacitance of 123.5 mF cm−2. Notably, the MSC demonstrates long-term stability up to the 5000th cycle with a capacity retention of 85.6 %, suggesting the electrode material has excellent mechanical flexibility and superior electrochemical performance.

Ecological Risk Assessment of Potentially Toxic Metals in Arable Soils around Adudu Lead – Zinc Mine, North-Central Nigeria

Mining is a major source of toxic heavy metals into the soil when mine wastes are discharged into the nearby farmlands used for the cultivation of food crops. This study investigated the influence of Pb–Zn mining on the quality and ecological risk of arable soils around active mining sites in Adudu, Nasarawa State, Nigeria. Composite soil samples were collected at 0–20 cm depth, pulverized, and analyzed for heavy metal (Al, As, Cr, Cu, Fe, Mn, Pb, and Zn) concentration using X–ray fluorescence technique. Enrichment factor, geo–accumulation index, improved Nemerow index (IIN), contamination factor (CF), degree of contamination (Cd), pollution load index (PLI), and ecological risk assessment (ERA) were used to evaluate the effect of the mining activities on the environment. Results showed elevated levels of Pb, Zn, Cu, Fe, Mn, and Cr in arable soils around the mine and lower levels of these metals in the control soil. IIN, Cd, and PLI showed that the mine and the nearby arable soils were the most deteriorated, and soil quality improved away from the mining vicinity. ERA revealed that the mine and the closest arable soils (sites F1 and F4) have significant to high ecological risk index as a result of the dominant presence of Pb, Zn, and Cu at the sites. Thus, arable soils which are disposal channels for mine wastes are not good for growing food crops. This study clearly shows that Pb–Zn mining activities introduced heavy metals into the arable soils surrounding the mine.

Assessment of water quality and associated human health risk of a tropical freshwater body in Edo State, Nigeria

The quality of freshwater sources is a key factor in sustainable development. This study investigated the water quality suitability of Ossiomo River for human consumption and the implications for public health. Water samples were collected and analysed from October 2021 to March 2022. Results indicated that the water physico-chemical parameters from sampled locations were within their respective National Environmental Standards and Regulation Enforcement Agency (NESRA) permissible limits except for pH (< 6.5), dissolved oxygen (< 6.0mg L−1), cadmium (> 0.005m /L−1), manganese (> 0.05mg L−1) and total hydrocarbon content (>10mg L−1). Comprehensive pollution index (0.4–1.0) and water quality index (251.57–765.37) values indicate that the water body was slightly polluted and unsuitable for human consumption (WQI > 50). Health risk assessment showed that children and adults were predisposed to non-carcinogenic risk (HIoral > 1) and carcinogenic risk (ICR: 1.21E-02 and 2.84E-03) from heavy metals through oral exposure. Natural run-off and anthropogenic activities were identified sources of heavy metals and hydrocarbons within the catchment. The study has provided data for water resource quality monitoring and raised concerns as to the need for immediate action to safeguard the public health of communities surrounding the Ossiomo River, through the provision of alternative sources of potable water.

Risk assessment of heavy metals in the freshwater lake sediments around Eppawala phosphate deposit, Sri Lanka

The Eppawala area in Sri Lanka has an agricultural-based economy. As a result, the recent agricultural intensification could increase the risk of heavy metal contamination in lakes in the area as the main water canal in the area, i.e., Jaya Ganga, flows across these lakes. Therefore, this study focuses on the risk assessment of heavy metals in the freshwater lake sediments in the Eppawala area and the identification of potential sources for heavy metal contamination in the lakes. Nine heavy metals (Cr, Mn, Co, Ni, Cu, Zn, As, Cd, and Pb) were investigated in surface sediments (n = 22) of the upstream and downstream lakes of the Eppawala Phosphate Deposit (EPD). The average heavy metal concentrations in the upstream lake sediments were higher than those downstream. Eppawala lake sediments were heavily polluted by As along with moderate to high Cr pollution. However, only As and Cd indicated considerable to moderate ecological risk levels to the local environment. The downstream lake sediments showed lower heavy metal contents compared to those upstream and had negative correlations between heavy metals and P2O5 contents. This reveals that the EPD does not contribute to the heavy metal contamination in the Eppawala lake sediments. However, the statistical analysis showed that heavy metals were mostly derived from similar pollution sources. Agrochemicals used in paddy cultivation in the vicinity might be a potential source of heavy metals. This study highlights the importance of implementing remediation to control the heavy metal pollution prevailing in the Eppawala lakes.

Exploration of ZnO-Doped Nitrogen-Carbon Materials Derived from Polyamide-Imide for Propane Dehydrogenation

A series of ZnO-doped nitrogen-carbon materials (xZnO-N-C) with ZnO contents of 5–40% are prepared by a vacuum curing–carbonization strategy using polyamide-imide as the N-C source and zinc nitrate as the metal source for propane dehydrogenation (PDH). 20ZnO-N-C exhibits outstanding initial activity (propane conversion of 35.2% and propene yield of 24.6%) and a relatively low deactivation rate (0.071 h−1) at 600 °C. The results of detailed characterization show that small ZnO nanoparticles (5.5 nm) with high dispersion on the catalyst can be obtained by adjusting the ZnO loading. Moreover, more nitrogen-based species, especially ZnNx species, are formed on 20ZnO-N-C in comparison with 20ZnO-N-C-air prepared via curing carbonization without vacuum, which may contribute to the higher product selectivity and catalytic stability of 20ZnO-N-C. The active sites for the PDH reaction on the catalyst system are proposed to be C=O species and Zn2+ species. Moreover, the carbon deposition and the aggregation of ZnO nanoparticles are the causes of activity loss on this catalyst system.

The elemental fingerprint as a potential tool for tracking the fate of real-life model nanoplastics generated from plastic consumer products in environmental systems.

Metals and metalloids are widely used in producing plastic materials as fillers and pigments, which can be used to track the environmental fate of real-life nanoplastics in environmental and biological systems. Therefore, this study investigated the metal and metalloids concentrations and fingerprint in real-life model nanoplastics generated from new plastic products (NPP) and from environmentally aged ocean plastic fragments (NPO) using single particle-inductively coupled plasma-mass spectrometry (SP-ICP-TOF-MS) and transmission electron microscopy coupled with energy dispersive X-ray spectroscopy (TEM-EDX). The new plastic products include polypropylene straws (PPS), polyethylene terephthalate bottles (PETEB), white low-density polyethylene bags (LDPEB), and polystyrene foam shipping material (PSF). All real-life model nanoplastics contained metal and metalloids, including Si, Al, Sr, Ti, Fe, Ba, Cu, Pb, Zn, Cd, and Cr, and were depleted in rare earth elements. Nanoplastics generated from the white LDPEB were rich in Ti-bearing particles, whereas those generated from PSF were rich in Cr, Ti, and Pb. The Ti/Fe in the LDPEB nanoplastics and the Cr/Fe in the PSF nanoplastics were higher than the corresponding ratios in natural soil nanoparticles (NNPs). The Si/Al ratio in the PSF nanoplastics was higher than in the NNPs, possibly due to silica-based fillers. The elemental ratio of Si/Al, Fe/Cr, and Fe/Ni in the nanoplastics derived from ocean plastic fragments was intermediate between the nanoplastics derived from real-life plastic products and NNPs, indicating a combined contribution from pigments and fillers used in plastics and from natural sources. This study provides a method to track real-life nanoplastics in controlled laboratory studies based on nanoplastic elemental fingerprints. It expands the realm of nanoplastics that can be followed based on their metallic signatures to all kinds of nanoplastics. Additionally, this study illustrates the importance of nanoplastics as a source of metals and metal-containing nanoparticles in the environment.

Synthesis and characterisation of novel metal-organic frameworks (MOFs) based on zirconium and bicinchoninic acid

Metal-organic frameworks (MOFs) are a relatively new class of materials of unique porous structures and exceptional properties. Currently, more than 110,000 types of MOFs have been reported among the countless possibilities. In this study, we have synthesised a novel MOF using zirconium chloride as the metal source and 4,4'-dicarboxy-2,2'-biquinoline (bicinchoninic acid disodium salt) as the linker, which reacted in N,N-Dimethylformamide (DMF) solvent. Three preparation methods were employed to prepare five types of the MOF, and they were compared to optimize the synthesis conditions. The resulting MOFs, named Zr-BADS, were characterised using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), microscopy, and X-ray diffraction (XRD). By incorporating methanol into the preparation solvent, the surface area was increased to 396 m2/g. Additionally, the prepared MOFs exhibited amorphous shapes, with variations in size depending on the synthesis method. This research demonstrates the significance of the preparation method in controlling resulting particles’ properties.

Solid-waste-recycled CuO/C3N4 S-scheme heterojunctions for efficient photocatalytic antibiotic degradation.

With the increasing severity of antibiotic pollution, the development of effective green photocatalysts for the degradation of organic pollutants in water has attracted extensive attention. Herein, we have prepared CuO/C3N4 S-scheme heterogeneous photocatalysts via recycling Cu resources from Cu-containing electroplating sludges. By mediating the acid leaching process, copper in electroplating sludges was dissolved selectively, while other metal species were retained in the residues. The CuO/C3N4 S-scheme heterojunction not only effectively suppressed the recombination of photogenerated charge carriers of C3N4, but also preserved the strong reducing electrons of C3N4 and the strong oxidizing holes of CuO, retaining the outstanding redox ability of CuO/C3N4. Therefore, CuO/C3N4 photocatalysts exhibited good catalytic performance in the degradation of tetracycline (over 95% in 2 h). In addition, CuO/C3N4 S-scheme heterojunctions achieved a high mineralization rate (45% in 2 hours), thus reducing secondary pollution during the degradation. This work provides a reliable direction for designing novel S-scheme heterojunction photocatalytic materials by using metal sources in solid waste.

Differential effects of two Zn sources (ZnO nanoparticles and ZnSO4) on lipid metabolism via the ferroptosis pathway and SLC7A11K23 acetylation by HDAC8 and HDAC6 in a freshwater teleost

Understanding the toxicity and hazard risk of various metal sources is very important and can provide new insights for their risk evaluation in the environment.

Mitochondrial topoisomerase 1 targeted anticancer therapy using irinotecan encapsulated mesoporous MIL-101(Fe) synthesized via a vapour assisted method.

Mitochondrial topisomerase 1 (Top1mt) is critical for mtDNA replication, transcription, and energy production. Here, we investigate the carrier-mediated targeted delivery of the anticancer drug irinotecan into the mitochondria to selectively trap Top1mt covalent complexes (Top1mtcc) and its role in anticancer therapeutics. We have designed a biocompatible mesoporous metal-organic framework (MOF) material, namely MIL-101(Fe), as the drug delivery carrier that selectively localizes inside mitochondria. In contrast to the traditional way of synthesising MOFs, here we have employed a vapour-assisted solvothermal method for the synthesis of MIL-101(Fe) using terephthalic acid as the organic linker and Fe(III) as the metal source. The advantage of this method is that it recycles the excess solvent (DMF) and reduces the amount of washing solvent. We demonstrate that MIL-101(Fe)-encapsulated irinotecan (MIL-Iri) was selectively targeted towards the mitochondria to poison Top1mtcc in a dose-dependent manner and was achieved at a low nanomolar drug concentration. We provide evidence that Top1mtcc generated by MIL-Iri leads to mtDNA damage in human colon and breast cancer cells and plays a significant role in cellular toxicity. Altogether, this study provides evidence for a new and effective strategy in anticancer chemotherapy.