Electromigration Research Articles

Environmental Implications of the Soil-to-Groundwater Migration of Heavy Metals in Mining Area Hotspots

Groundwater contamination was studied at several hotspot sites in the Majdanpek copper mining area (Serbia). These sites include a milling facility, a metallurgical wastewater treatment plant, a heavy vehicle service area, and a waste disposal site. In addition to Cu, high concentrations of As and heavy metals (Cd and Pb) were detected in groundwater and soil at the same sampling points. Mining operations and heavy vehicle transport activities have been identified as the main sources of pollution. The migration of metals from soil to groundwater, expressed as a concentration ratio, were the highest for Co and the lowest for Mn. The environmental implications of groundwater pollution were studied using the heavy metal pollution index (HPI), Nemerov pollution index (NPI), hazard index (HI), and incremental lifetime cancer risk (ILCR). HPI and NPI show the high potential of groundwater to have adverse environmental effects. HPI ranges in the following descending order of metals: Cd > Pb > As > Mn > Ni > Cr > Hg > Cu > Zn. NPI exceeds the threshold of 0.7 in 66.7% of the samples. Potential human exposure to the studied groundwater may cause severe health problems in adults, with HI ranging from 0.61 to 5.45 and ILCR from 1.72 × 10−4 to 1.27 × 10−3. Children were more susceptible to non-carcinogenic risk than adults, with HI ranging from 0.95 to 8.27. However, the results indicated that children were less prone to carcinogenic risks, with ILCR ranging from 5.35 × 10−5 to 3.98 × 10−4. Arsenic is the most contributing element to both risks. This research imposes the need for enhanced groundwater monitoring at hotspots in the mining area and the adoption of remediation plans and measures.

Geoenvironmetal assessment of different types of cryolithic soils in Western Yakutia under the conditions of diamond-mining operations

The problems of geoenvironmental consequences of mining operations are especially acute in the arctic and subarctic regions, where the spread of permafrost significantly reduces the buffering capacity of landscapes. The article presents data on the content of heavy metals in the soil cover of the transient zone between the middle taiga and north taiga landscapes of Western Yakutia under the conditions of mining operations and assesses the resistance of different types of soils to heavy metals pollution. Field and laboratory works were carried out in August 2022. The heavy metals content was determined by atomic absorption spectrometry. Specialized software was used for analysis, such as MS Excel 2013, Statistica 12.0, and QGis 3.26.1. Calculation of organic forms of heavy metals in soil solutions was performed using the NICA-Donnan model. In the course of studies, the structure of the soil cover in the Nakyn kimberlite field in the conditions of the mining industrial complex operation was determined and a sketch map of the soil cover of the territory was compiled. The geochemical series of the studied heavy metals is as follows according to the degree of concentration of heavy metals in cryolithic soils: Pb > Zn > Ni > Cu > Cd > As > Hg. Positive correlations between humus and Cd, Pb, Zn, as well as the occurrence of synergism in the Pb–Cd, Zn–Pb, Zn–Cu pairs were revealed. The soils organic matter enhances migration of heavy metals. The man-made input of Ni and Zn in cryolithic soils will lead to increase of mobile fraction. Cd is more mobile in pale-yellow carbonate and cryogenic soils. The regional background level of heavy metals for these types of soils was calculated, which can be used in future works when the intensity of mining operations increases.

Material flow analysis of heavy metals in large-scale cattle farms and ecological risk assessment of cattle manure application to fields

This study bridges the knowledge gap pertaining to the pathways of heavy metal accumulation and migration within the industrial chain of large-scale cattle farms. Two such farms in Shaanxi serve as a basis for our exploration into Zn, Cu, Cr, Pb, As, and Cd dynamics. Employing material flow analysis complemented by predictive models, we evaluate the potential ecological risks of arable soil from heavy metal influx via manure application. Our findings indicate that Zn and Cu predominate the heavy metal export from these operations, composing up to 60.00%–95.67% of their total content. Predictive models based on 2021 data reveal a potential increase in Cd soil concentration by 0.08 mg/kg by 2035, insinuating a reduced safe usage period for cattle manure at less than 50 years. Conversely, projections from 2022 data point towards a gradual Cu rise in soil, reaching risk threshold levels after 126 years. These outcomes inform limitations in cattle manure utilisation strategies, underscoring Cu and Cd content as key barriers. The study underscores the criticality of continuous heavy metal surveillance within farm by products to ensure environmental protection and sustainable agricultural practices.

Improving the performance of iron-rich calcium sulfoaluminate cement from municipal solid waste incineration fly ash through diverse pretreatment approaches

The utilization of municipal solid waste incineration fly ash (MSWI-FA) is environmentally significant. In this study, MSWI-FA was pretreated using organic acid solution and CO2 microbubble carbonation washing. The pretreated MSWI-FAs were then used to produce Iron-rich calcium sulfoaluminate (IR-CSA) cement at different substitution rates (CFA) for various raw materials. The evolution of iron phase distribution, mineral composition, and hydration of IR-CSA cement were investigated, alongside heavy metal migration. The results showed that the MSWI-FA-based IR-CSA clinker had suitable mineralogical phases. However, gehlenite in MSWI-FA reduced CaO availability in the clinker formation reaction, hindering the involvement of Fe2O3 in the ye'elimite formation reaction. The calcination temperature was increased to facilitate clinker and iron phase formation in the case of high CFA levels. CO2 microbubble carbonation washing pretreatment of MSWI-FA, with which the IR-CSA clinker achieved suitable pH values and alkali content, facilitated the early growth and chained evolution of ettringite, resulting in a denser microstructure and lower cumulative hydration heat. Consequently, the compressive strength of MSWI-FA-based IR-CSA cement increased, with a maximum gain of 43.65 MPa. Chromium content in the residual form increased, and heavy metal leaching was well below standard limits. This approach provides a new perspective for the purification treatment of MSWI-FA and its high-value, large-scale recycling in low-carbon cement.

Effects of woodland slope on heavy metal migration via surface runoff, interflow, and sediments in sewage sludge application

Sewage sludge (SS) application to forest plantation soils as a fertilizer and/or soil amendment is increasingly adopted in plantation forest management. However, the potential risks of SS-derived heavy metals (HMs) remain a concern. Many factors, including woodland slope may affect the risks, but the understanding of this issue is limited. This research evaluated the HMs migration via surface runoff, interflow, and sediments when SS was applied in woodlands of varying slopes. We conducted indoor rainfall simulations and natural rainfall experiments to clarify the effect of slope on the migration of HMs via runoff (including surface and interflow) and sediments. In the simulated rainfall experiment, HMs lost via sediments increased by 9.79–27.28% when the slope increased from 5° to 25°. However, in the natural rainfall experiment, when the slope of forested land increased from 7° to 23°, HMs lost via surface runoff increased by 2.38% to 6.13%. These results indciate that the surface runoff water on a high slope (25°) posed high water quality pollution risks. The migration of HMs via surface runoff water or interflow increased as the steepness of the slope increased. The total migration of Cu, Zn, Pb, Ni, Cr and Cd via sediment greatly exceeded that via surface runoff and interflow. Particles ≤ 0.05 mm contributed the most to the ecological risks posed by sediments. Cd was the main source of potential ecological risks in sediments under both experimental conditions.

Energy recoveries and heavy metal migration behaviors of different oily sludges treated by pyrolysis versus solvent extraction

The pyrolysis and trace element mitigation characteristics are investigated by contrast to solvent extraction for four oily sludges, including storage tank bottom sediment (OS-1), scum from a wastewater separator (OS-2), white-clay-adsorbed waste oil (OS-3), and settlings from wastewater treatment (OS-4). Slow pyrolysis at 700 °C generated a single oil phase for OS-1 and separate oil and aqueous phases for OS-2, OS-3 and OS-4. Up to 73.0–88.3 % of the total energy were recovered from OS-1, OS-2 and OS-3 in the oil phase with 19.9–77.1 % oil yield; however, the oil phase from OS-4 accounted for only 13.3 % of the total energy, while the aqueous product accounted for 68.0 % of the total energy. Quantification of 16 trace elements revealed that OS-2 and OS-4 had much higher contents of Cu/Zn/As/Se/Cd/Pb and Ni/Cu/Zn/Se/Cd contents than the average crustal abundances, respectively. Correlations between evaporation and extraction rates indicated that the mitigation behaviors of trace elements were related to their occurrence modes in different oily sludges. Except for Cd, As and Se, all other trace elements were enriched in the pyrolysis residues of the oily sludges. Ni in the pyrolysis residue of OS-4 posed a moderate potential ecological risk.

Molecular Basis of Energy Crops Functioning in Bioremediation of Heavy Metal Pollution

Heavy metal pollution is a gradually growing environmental issue that hinders the growth and development of plants, and also destabilizes soil. Consequently, eco-friendly phytoremediation methods have gained traction, with energy crops emerging as a particularly effective solution. Energy crops not only provide high-quality plant materials for detoxification and remediation of heavy metal pollution, but also possess energy properties conducive to biofuel production. Therefore, this paper delves into the tolerance mechanism of energy crops towards heavy metal toxicity, elucidating processes such as root complex-mediated inhibition of metal migration and response to reactive oxygen species (ROS) through heavy metal-related proteins, enzyme systems, reactive nitrogen species (RNS), and hormones. Moreover, it summarizes the heavy metals remediation mechanisms of energy crops, including uptake, translocation, chelation, immobilization, and sequestration. This paper explores applications of energy crops in heavy metal pollution remediation, emphasizing the methods for efficient biochar remediation and biofuel generation. Furthermore, potential challenges in using energy crops for heavy metal pollution remediation are outlined. By systematically examining the function mechanisms and prospective applications of energy crops in heavy metal pollution bioremediation, this paper serves as a valuable reference for both research and practical implementation in this field.

Integrating diffusion dialysis for sustainable acid recovery from ion exchange regeneration stages: Characterization of metal and non-metal ions migration

Seawater mining presents a potential option for recovering the European Union’s Critical Raw Materials (CRMs), but direct extraction from seawater is challenging due to their low concentrations, as most of them are Trace Elements (TEs) (at levels of mg/L or µg/L). Saltworks bitterns (ultraconcentrated brines resulting from the sea salt production process) offer an alternative solution, naturally concentrated up to 40 times more than seawater. These bitterns can be further processed with chelating Ion Exchange (IX) sorbents to selectively extract TEs. However, this process requires an acidic elution stage with strong acids, followed by neutralization, to recover TEs through precipitation, demanding extensive chemicals consumption. Diffusion Dialysis (DD) could be used to recover the excess acid without external reagents, using an acid-resistant Anion Exchange Membrane (AEM). This study evaluates DD through batch and once-through tests for acid recovery from simulated IX eluate generated in the elution stage of TEs (B, Ga, Ge, Co, Sr) recovery from saltworks bitterns.Batch tests achieved high recoveries for HCl (45–50 %) and H2SO4 (30–37 %), being the theoretical maximum attainable recovery equal to 50 %. B and Ge only partially permeated through the membrane (82 % rejection) by a diffusion mechanism in their neutral form (H3BO3(aq), H4GeO4(aq)). Ga, Co and Sr, in cationic form, were highly rejected (>96 %). Permeability followed the order Ga < Sr < Co ≪ Ge < B, due to the relevant charge and size. HCl permeability correlated linearly with concentration, while H2SO4 was inversely proportional. Once-through tests showed higher acid (74 % HCl, 62 % H2SO4) and oxoacid (66 % H3BO3(aq), 52 % H4GeO4(aq)) recovery at a low specific flow rate, or apparent flux, (0.38 L/(m2membrane·h)) due to increased residence time. Water to acid flow rate ratios did not affect species transport when an excess of water was guaranteed. Conversely, an influence was observed when the ratio was below 1, with a minimum at 0.18, where a very low passage of species was observed due to the reduced dilution volume of the dialysate solution (water). A 1D transport model, incorporating the solutes permeabilities determined experimentally, effectively described the system performance, especially for HCl and B, albeit slightly overestimating the other TEs’ transport.

Highly reversible transition metal migration in superstructure-free Li-rich oxide boosting voltage stability and redox symmetry

The further practical applications of Li-rich layered oxides are impeded by voltage decay and redox asymmetry, which are closely related to the structural degradation involving irreversible transition metal migration. It has been demonstrated that the superstructure ordering in O2-type materials can effectively suppress voltage decay and redox asymmetry. Herein, we elucidate that the absence of this superstructure ordering arrangement in a Ru-based O2-type oxide can still facilitate the highly reversible transition metal migration. We certify that Ru in superstructure-free O2-type structure can unlock a quite different migration path from Mn in mostly studied cases. The highly reversible migration of Ru helps the cathode maintain the structural robustness, thus realizing terrific capacity retention with neglectable voltage decay and inhibited oxygen redox asymmetry. We untie the knot that the absence of superstructure ordering fails to enable a high-performance Li-rich layered oxide cathode material with suppressed voltage decay and redox asymmetry.

Cu doping in TM ordered and disordered layered oxides for Sodium-Ion Batteries: Electrochemical Properties, structure evolution and Cu-Ion migration

The ordered/disordered distribution of transition metal (TM) plays a significant role in determining electrochemical properties including lattice oxygen redox, ion kinetics and structure evolution. From a novel perspective, this work demonstrates how the TM distributions influence the doping effect by means of introducing Cu element into ordered/disordered O3-Nax(NiySb1-y)O2. What’s more, the irreversible Cu migration from TM sites to Na layers upon electrochemical process is found. This migration which would deteriorate electrochemical stability only occurs in honeycomb-ordered compounds, instead of in disordered one. Theoretical calculations reveal that the TM disordered distribution promotes the formation of antibonding orbitals between Cu 3d and O 2p, thereby increasing the barrier of Cu migration to maintain well Na diffusion kinetics. Our discovery rolls out a new guidance for designing advanced cathode materials for sodium-ion batteries and speeds up the research on transition metal migration.

Regulating anionic redox reversibility in Li-rich layered cathodes via diffusion-induced entropy-assisted surface engineering

Cobalt-free lithium- and manganese-rich layered oxides (LMROs) are regarded as effective cathode materials for lithium storage due to their high capacity and cost-effectiveness. However, challenges with structural degradation, resulting in poor cyclability and rate performance, have hindered their widespread use. Essentially, rapid structural degradation arises from irreversible and complex redox reactions, triggering oxygen release, transition metal migration, and electrolyte decomposition. To tackle this issue, we propose an epitaxial entropy-assisted construction approach to develop a sturdy surface with adaptable composition, stabilising the surface crystal structure and preventing undesirable interface reactions. This distinct reconstructed surface comprises diverse heterogeneous elements and composite microstructures. The heteroatom-doped layer, with multi-doping sites like Li, O site, and tetrahedral positions, effectively manages the chemical environment and electronic structure of surface lattice oxygen. This epitaxial entropy stabilisation approach, stemming from multi-element synergy, effectively controls redox progress to limit oxygen release and curb transition metal migration, reducing structural decay. Additionally, the composite coated layer, containing oxygen defects and heterogeneous spinel phases, can hinder electrolyte corrosion and promote Li+ transport. Using these epitaxial entropy surface modifications, the LMRO cathode demonstrates regulated anionic redox reversibility and enhanced cycling stability across diverse operational conditions. This epitaxial entropy-assisted surface engineering offers a promising avenue for stabilising high-energy cathode materials.

Constructing partially spinel phase in Mn-rich cathode material

As a cathode with earth-abundant element, Mn-rich oxide has been explored to enable the scaling of the Li-ion battery. However, the irreversible transition metals migration and phase transformations in Mn-rich materials have been proven to be detrimental, which trigger capacity degradation, voltage decay, and poor kinetics. In this work, using Li2MnO3 as model, spinel-layered biphase was constructed via Ti doping and de-lithiation modification, which exhibits higher available capacity of 236.9 mAh/g (55.6 mAh/g for pristine material) and improved rate performance. Compared with pristine Mn-based cathodes, the new phase delivers neglectable voltage degradation during electrochemical cycling. Based on systematic characterization, the new phase exhibits higher oxygen redox reversibility and accelerated kinetics of lithium ions transformation. This work provides a new strategy for designing high-energy density Mn-rich cathodes.

Iron Plaque: A Shield against Soil Contamination and Key to Sustainable Agriculture.

Soils play a dominant role in supporting the survival and growth of crops and they are also extremely important for human health and food safety. At present, the contamination of soil by heavy metals remains a globally concerning environmental issue that needs to be resolved. In the environment, iron plaque, naturally occurring on the root surface of wetland plants, is found to be equipped with an excellent ability at blocking the migration of heavy metals from soils to plants, which can be further developed as an environmentally friendly strategy for soil remediation to ensure food security. Because of its large surface-to-volume porous structure, iron plaque exhibits high binding affinity to heavy metals. Moreover, iron plaque can be seen as a reservoir to store nutrients to support the growth of plants. In this review, the formation process of iron plaque, the ecological role that iron plaque plays in the environment and the interaction between iron plaque, plants and microbes, are summarized.

Comparative study of iron and aluminium coagulants in conditioning sludge: Sludge dewatering performance, physicochemical properties, and risk of heavy metal migration

Inorganic coagulants are essential agents that can facilitate the sludge deep dewatering, but comprehensive comparative research of commonly used coagulants is lacking. The systematic comparison of six coagulants, including Ferric Chloride (FeCl3), Polymeric Ferrous Sulfate (PFS), Ferrous Sulfate (Fe2(SO4)3), Aluminium Chloride (AlCl3), Aluminium Sulfate (Al2(SO4)3), and Polymeric Aluminium Chloride (PAC) regarding their performance in conditioning sludge dewatering, physicochemical properties, the risk of heavy metals migration in sludge cake and the mechanism of sludge dewatering, was investigated. Within a dosage range of 20% dry solids (DS), the PFS and FeCl3 showed a better dewatering effect among the six coagulants, and the water content (Wc) of the sludge cake decreased from 81.2%±1.1% to 57.7%±1.0% and 59.2%±1.6%, respectively. There was a correlation between the pH, zeta potential, viscosity, and bound water content of the sludge and the Wc of the sludge cake during dewatering conditioned by six coagulants. However, there was no correlation between sludge particle size and Wc of the sludge cake. The PFS and FeCl3 reduced the protein content of tightly bound extracellular polymeric substances (TB-EPS) by 66.1% and 62.6%, respectively. Moreover, the iron coagulants significantly reduced the content of As, Cu, Ni, and Zn in the sludge cake, where the risk levels of As and Ni were largely weakened. The economic analysis shows that iron coagulants were more valuable than aluminium coagulants for engineering applications. Meanwhile, the dewatering mechanisms of the two types of coagulants were revealed. This study provides significant insights into the application of coagulants in engineering practice.

Sewage sludge enhances cold-pressed pelletization and carbothermic reduction of steel plant sintering dust

The sludge-based forming thermal reduction can be used to improve the resource utilization ability of sintering dust. This paper discussed the feasibility and mechanism of sewage sludge as a binder and reducing agent to facilitate iron recycling from sintering dust by mixing wet sludge to form and adding dry sludge to reduce. The results showed that a 1.4% ratio of sewage sludge significantly enhanced the strength of metallurgical pellets, and the compressive strength of wet and dry pellets reached 309.5 and 1233.5 N/P. Meanwhile, with the addition of dry sludge (S/Fe = 2.0), the metallization ratio can be up to 88.4%. Sewage sludge has a more efficient reduction potential than other carbon sources as reducing agents. Combined with XRD, XPS, TG-MS, TG-FTIR, and other characterization methods, the reduction phenomenon of iron was confirmed, and the migration and transformation of metals in sintering dust and the segmented volatilization rule of Pb, Zn, K, Na, and other elements were revealed. It is proven that sludge as the disposal route of metallurgical dust cold-pressed forming and reduction is a green and sustainable view and promising research direction.

Colloidal carbon soot templated TiO2/Ag surface functionalized 3D printed metal brushes as new generation surface enhanced Raman scattering substrates

This present work demonstrated the functional transformation of 3D printed metal substrates into a new family of Surface-enhanced Raman Scattering substrates, a promising approach in developing SERS-based Point-of-care (PoC) analytical platforms. l-Powder Bed Fusion (l-PBF, Additive manufacturing or 3D printing technique) printed metal substrates have rough surfaces, and exhibit high thermal stability and intrinsic chemical inertness, necessitating a suitable surface functionalization approach. This present work demonstrated a unique multi-stage approach to transform l-PBF printed metal structures as recyclable SERS substrates by colloidal carbon templating, chemical vapor deposition, and electroless plating methods sequentially. The surface of the printed metal structures was functionalized using the colloidal carbon soot particles, that were formed by the eucalyptus oil flame deposition method. These carbon particles were shown to interact with the metals present in the printed structures by forming metal carbides and function as an adlayer on the surface. Subsequent deposition of TiO2 onto these templates led to strong grafting of TiO2 and retaining the fractal structure of the soot template onto the metal surface. Electroless deposition of silver nanoparticles resulted in the formation of fractally structured TiO2/Ag nanostructures and these functionalized printed metal structures were shown as excellent SERS substrates in enhancing the vibrational spectral features of Rhodamine B (RhB). The presence of TiO2 photocatalyst on the surface was shown to remove the RhB analyte from the surface under photochemical conditions, which enables the regeneration of SERS activity, and the substrate can be recycled. The migration of metals from the printed metal structures into the fractally ordered TiO2/Ag nanostructures was found to enhance the photocatalytic activity and increase the recyclability of these substrates. This study demonstrates the potential of 3D-printed Inconel metal substrates as next-generation recyclable SERS platforms, offering a substantial advancement over traditional colloidal, thin-film, flexible, and hard SERS substrates.

Study on Plant-blanket to reduce heavy metal migration caused by precipitation and to improve the soil environment of pyritic tailings

The increasing demand for mineral resources due to industrial development has led to significant tailings pollution during the mineral extraction process. In the southwestern region of China, a large amount of pyritic tailings containing pyrite cinder easily leaches heavy metals and other pollutants when exposed to precipitation, resulting in widespread soil contamination. Effective remediation methods are urgently needed to address this issue. This study utilized naturally occurring Plant-blanket formed by the symbiosis of moss and herbaceous plants on pyritic tailings as restoration material. Through leaching experiments and staining tracer techniques, the study investigated the ability of Plant-blanket to reduce the migration of heavy metals from pyrite cinder to soil under the influence of precipitation and its role in improving the soil environment. The results showed that within 12 h, the Plant-blanket could absorb water equivalent to 206.9 % of its own weight and had good water retention ability. It reduced the stained area ratio of soil horizontal and vertical profiles after precipitation leaching by a maximum of 76.08 % and 46.41 %, respectively, and improved the pH, cation exchange capacity (CEC), bulk density, and water content of soil at different depths. In addition, after being covered by Plant-blanket, the migration of Cd and Cu was reduced by a maximum of 44.35 % and 55.77 % respectively, and it increased the diversity and abundance of bacterial communities, promoting the recovery of soil microbial ecological functions. These findings indicate that Plant-blanket can regulate water and improve soil environment, and has certain control ability on the migration of Cd and Cu produced by pyritic tailings. Meanwhile, Plant-blanket plays an important role in improving the soil environment in mining areas and promoting ecosystem restoration, providing valuable reference for further exploration of ecological restoration of tailings.

Theoretical study on catalytic performance of Ti2B monolayer as cathodes of Li-O2 and Na-O2 batteries promoted by surface functionalization

Alkali metal–oxygen batteries with high theoretical energy density are regarded as one of the promising next-generation batteries. The suitable catalyst is the key to realize the application of alkali metal–oxygen batteries. In this study, two-dimensional (2D) Ti2B monolayer with extremely high Young’s modulus (1024.7 N·m−1) was investigated as cathode catalysts of Li-O2 and Na-O2 batteries by density functional theory (DFT) calculations. The electrocatalytic performance can be further improved by surface functionalization, and the catalytic activities based on total overpotentials are in order: Ti2BF2 (1.244/1.131 V) < Ti2BCl2 (1.383/1.247 V) ≈ Ti2BS2 (1.373/1.256 V) < Ti2B (9.514/9.191 V) for both Li-O2 and Na-O2 batteries. Furthermore, there is a volcanic relationship between overpotentials and the binding energies of peroxides and substrates. The energy evolution of four-electron steps on these materials reveals that surface functionalization regulated catalytic activities by balancing the adsorption strength of alkali metal and oxygen, and the disproportionation side reactions on surface functionalized Ti2B monolayers are thermodynamically unfavorable. Besides, the densities of states (DOSs) and alkali metal migration behaviors of these materials indicate their good electronic and ionic conductivities. Our study of functionalized Ti2B monolayer cathode catalysts may shed light on the application of 2D transition metal borides to alkali metal–oxygen batteries.

Exploration indication of hidden gold deposits using the fine-grained soil prospecting method and its nano-micron metal migration evidence in the alluvial soil covered area, Jiaodong

Jiaodong stands out among three global provinces boasting gold reserves surpassing 5000 tons. As geological exploration in the region continues to rise, the significance of deep and covered areas in Jiaodong for ore prospecting becomes increasingly evident. In this study, a Fine-grained soil prospecting method was employed in the Qujia hidden gold deposit and its surrounding region, situated in Yantai City, Shandong Province, and concealed by alluvial soil. The gold (Au) content exhibited a high enrichment level, and the range of Au and silver (Ag) geochemical anomalies demonstrated a robust correlation with known hidden orebodies. Furthermore, transmission electron microscopy and nano-CT were utilized to identify nano-micron metal particles and micro-fractures in the wall rock. A hereditary relationship between the nano-micron metal particles of ore-forming elements present in surface media and the deep orebody was observed. A migration model detailing the movement of deep ore-forming materials in the form of nano-micron metal particles, governed by a multi-agent relay dominated by ascending geogas flow, was established in the Qujia gold deposit in Jiaodong. These findings contribute theoretical support for the fine-grained soil prospecting method in geochemical exploration within alluvial soil covered areas.

Pollutant Emissions and Heavy Metal Migration in Co-Combustion of Sewage Sludge and Coal

The treatment of sewage sludge has become a global concern. Large amounts of sewage sludge can be disposed of by burning coal-mixed sludge. Thermogravimetric analysis and lab-scale combustion experiments in a drop tube furnace were utilized to study the combustion characteristics, pollutant emissions, and heavy metal migration during the co-combustion of coal and sewage sludge. The results showed that the blended fuels with a sewage sludge content less than 10 weight percent exhibited coal-like combustion characteristics. Additionally, the additional sewage sludge favored the ignition performance of blended fuels. When sewage sludge was added, the SO2 emissions rose to 76 mg/Nm3 under the 10% sludge condition—nearly three times higher than that of coal alone. While NOx emissions stayed mostly unchanged, HCl and HF emissions were very low. Meanwhile, Cr, Cu, and Ni migrated to the bottom ash, and their concentrations were all reduced with an increase in sewage sludge. Pb, Cd, Cr, Cu, Ni, and Hg migrated to the flue gas, mostly in the form of gaseous components. The results provide crucial information in the co-combustion of sewage sludge and coal, with implications in the development and improvement of large-scale, harmless, and resource-recovering techniques for waste sludge.