Search Results (154)

Biological reduction of sulphates has gradually replaced unit chemical processes for the treatment of acid mine drainage (AMD), which exerts a significant environmental impact due to its elevated acidity and high concentrations of heavy metals. Bioremediation is optimally suited for the treatment of AMD because it is cost-effective and efficient. Anaerobic bioremediation employing sulphate-reducing bacteria (SRB) presents a promising solution by facilitating the reduction of sulphate to sulphide. The formed can precipitate and immobilise heavy metals, assisting them in their removal from contaminated wastewater. This paper examines the current status of SRB-based bioremediation, with an emphasis on recent advances in microbial processes, reactor design, and AMD treatment efficiencies. Reviewed studies showed that SRB-based bioreactors can achieve up to 93.97% of sulphate reduction, with metal recovery rates of 95% for nickel, 98% for iron and copper, and 99% for zinc under optimised conditions. Furthermore, bioreactors that used glycerol and ethanol as a carbon source improved the efficiency of sulphate reduction, achieving a pH neutralisation from 2.8 to 7.5 within 14 days of hydraulic retention time. Despite the promising results achieved so far, several challenges remain. These include the need for optimal environmental conditions, the management of toxic hydrogen sulphide production, and the economic feasibility of large-scale applications. Future directions are proposed to address these challenges, focusing on the genetic engineering of SRB, integration with other treatment technologies, and the development of cost-effective and sustainable bioremediation strategies. Ultimately, this review provides valuable information to improve the efficiency and scalability of SRB-based remediation methods, contributing to more sustainable mining practices and environmental conservation. To ensure relevance and credibility, relevance and regency were used as criteria for the literature search. The literature sourced is directly related to the subject of the review, and the latest research, typically from the last 5 to 10 years, was prioritised. Full article

The mangrove wetland of the Dongzhai Harbour, located in northeastern Hainan, is of high ecological value. However, environmental pollution brought by the current rapid economic development, especially the pollution of heavy metals and reduced inorganic sulphur, puts the ecological environment of this region at risk. As the main carrier of these two kinds of pollution, sediments are deeply involved in their biogeochemical cycles. Therefore, in this study, surface sediments of mangrove wetlands in the Dongzhai Harbour were collected, and their concentration characteristics and sources of reductive inorganic sulphur (RIS) forms and heavy metals were investigated. The average RIS concentrations of the sediments in the study area were about 22.31 μmol/g, among which acid volatile sulphide (AVS) had the highest weight (ave. 10.01 μmol/g), followed by chromium (II)-reducible sulphur (CRS) with the average concentrations of 8.46 μmol/g, and elemental sulphur (ES) (3.84 μmol/g), which had the lowest concentration. The spatial distributions of different RIS forms were differentiated, reflecting the diversity of environments in the study area. Correlation analyses showed that the RIS forms, such as AVS and CRS, were mainly enriched in clay-sized sediments with p < 0.05. Compared to other areas of the world, the present study area was less contaminated by RIS. Ratio calculation revealed that the reducing environment in the study area limited the conversion of AVS to CRS in the sediments. Among the heavy metals, Cr (70.03 mg/kg) was the most abundant, followed by Zn, Pb, and Ni with an average of >20 mg/kg, while other elements such as As, Cd, Cu, Hg, and Co were found to be low (<18 mg/kg). Correlation analyses revealed that clay-sized sediments significantly constrained Ni, Zn, and Co and could effectively bind to AVS (p < 0.05). Based on cluster analysis, it was found that agricultural activities, mariculture, and transport mainly influenced heavy metals and RIS of sediments in the study area. The study helps understand the pollutant cycle in shelf wetland sediments and provides practical guidance for the sustainable development of ecosystems. In the future, it is recommended that reasonable control of pollution emissions be implemented in relevant areas. Full article

Copper is a critical metal required for green energy technologies such as wind turbines and solar cells. However, copper supply is limited by copper recovery from primary copper sulphides (e.g., chalcopyrite-CuFeS₂) due to passivating reaction products. Therefore, this study examined surface ‘passivation’ of primary copper sulphide minerals undergoing coupled dissolution with reprecipitation (CDR) reactions and the associated mineral surface changes in acidic and chloride-rich lixiviants (FeCl₃-only, AlCl₃-rich, NaCl-rich, and CaCl₂-rich lixiviants). Acidic FeCl₃-only, NaCl-rich, and CaCl₂-rich lixiviants resulted in only bornite dissolution and the formation of a residual Cu-S phase and Fe-SO₄ phase on the chalcopyrite surface. In contrast, leaching with the AlCl₃-rich lixiviant resulted in both chalcopyrite and bornite dissolution with limited hydrolysis of Fe³⁺ to Fe-hydroxy sulphates and minimal Fe³⁺ flux inhibition to the copper sulphide minerals surface due to the ion exchange mechanism between Al³⁺ and Fe³⁺. Further, there was preferential formation of an Al-SO₄ phase at consistently high Eh and acidity, thereby a high availability of Fe³⁺ in solution for enhanced copper dissolution from both bornite and chalcopyrite. These findings could serve as a reference for coupled dissolution with reprecipitation reactions during copper sulphide leaching, offering a pathway to more efficient and sustainable copper extraction from low-grade ores. Full article

As challenges in precious and base metal exploration intensify due to the diminishing availability of high-grade ore deposits, rising demand, energy costs, and stricter regulations towards net-zero carbon activities, advanced techniques to enhance exploration efficiency are becoming increasingly critical. This study demonstrates the effectiveness of quantitative X-ray diffraction (QXRD) with Rietveld refinement, coupled with multivariate statistical analysis (including agglomerative hierarchical clustering, principal component analysis, and fuzzy analysis), in characterizing the complex mineralogy of strata-bound volcanic-associated limestone-skarn Zn-Pb-Ag-(Cu-Au)-type sulphide deposits (SVALS). Focusing on 113 coarse rejects from the Gumsberg project located in the Bergslagen mining district in central Sweden, the research identified five distinct mineralogical clusters corresponding to polymetallic base metal sulphide mineralization, its proximal alteration zones, and variably metamorphosed host rocks. The results reveal significant sulphide mineralization, ranging from disseminated to massive occurrences of sphalerite, pyrrhotite, pyrite, and galena, with trace amounts of secondary minerals like anglesite in certain samples indicating weathering processes. The study also identifies rare minerals such as armenite, often overlooked in traditional geological logging. These findings underscore the potential of QXRD to enhance resource estimation, optimize exploration strategies, and contribute to more efficient and sustainable mineral exploration programs. The accuracy of QXRD was cross-validated with geological logs and geochemical data, confirming its reliability as a mineralogical discrimination tool. Full article

The Batailing Au deposit is a vein-type deposit in central Jilin Province, situated in the southern sector of the Lesser Xing’an–Zhangguangcai Range within the eastern Central Asian Orogenic Belt. NE-trending fault-controlled orebodies occur in the Upper Permian Yangjiagou Formation and quartz diorite–porphyrite. The mineralisation process was delineated into three stages: (I) quartz–arsenopyrite–pyrite, (II) quartz–polymetallic sulphides (main Au mineralisation stage), and (III) quartz–pyrite–carbonate. Fluid inclusions (FIs) in quartz were identified as four types: PC-type (pure CO₂), C₁-type (CO₂-bearing), C₂-type (CO₂-rich), and W-type (aqueous two-phase). Raman spectroscopy analysis revealed that the vapor components of the FIs predominantly comprised CO₂ with minor quantities of CH₄ in stages I–II. Stages I and II encompassed four types of FIs with homogenisation temperature ranging from 264 to 332 °C and 213 to 292 °C and salinity spanning from 4.7 to 11.2 wt% and 1.8 to 11.6 wt%, respectively. Stage III exclusively contained W-type FIs with homogenisation temperature ranging from 152 to 215 °C and salinity spanning from 1.4 to 6.4 wt%. H-O isotopic values (δD = −84 to −79.6‰, δ¹⁸O_H2O = 6.2 to 6.4‰ in stage I and δD = −96.4 to −90.4‰, δ¹⁸O_H2O = 2.8 to 4.4‰ in stage II) and microthermometric data indicated that the ore-forming fluids are initially from a magmatic source, with later meteoric water input. Low C isotopic data from CO₂ in FIs in quartz (−24.4 to −24.3‰ in stage I and −23.7 to −22.6‰ in stage II) indicated an organic carbon source. Ore precipitation is mainly attributable to fluid immiscibility. S-Pb isotopic data (δ³⁴S = −3.5 to −1.6‰; ²⁰⁶Pb/²⁰⁴Pb = 18.325–18.362, ²⁰⁷Pb/²⁰⁴Pb = 15.523–5.562, ²⁰⁸Pb/²⁰⁴Pb = 38.064–38.221) revealed that ore metals primarily originated from magma. Based on this research, the origin of the Batailing Au deposit is of the mesothermal magmatic–hydrothermal lode type. Full article

This short paper analyses the concentrations of two major components (Fe, S) and eight trace elements (As, Au, Co, Cu, Hg, Ni, Mn, Zn) in soils and tailings from Tierra Amarilla (northern Chile) using ICP-Ms analysis. The levels of As, Au, Cu, Fe and S are very high and come from polymetallic sulphides from nearby mines, together with minor contributions of Co, Ni and Mn. Hg has its origin in the extreme seasonal flows of the Copiapó River, which erodes the dumps of old precious metal mines. These high concentrations require further analysis of possible metal immobilisation techniques, bioavailability or analysis in cultivated plants. Full article

Variations in the recovery of platinum group metals (PGMs) are often attributed to mineralogical and other natural ore-type variations. To increase the recovery of PGMs by the flotation process, a comprehensive understanding of gangue and valuable minerals is essential for optimising the extraction and processing of metals. Recoveries may be improved if the questions of how, where, and why losses occur can be answered with a certain degree of confidence. A requirement is the availability of statistically reliable mineralogical data. The PGMs of MG-1–4 chromite tailings dumps of the western limb of the Bushveld complex (BC) were studied in detail to unravel the PGMs and the nature of the platinum group minerals in the sample. Characterisation of the chromite tailings via deportment analysis revealed that the sample contained a significant amount of 3E PGM + Au (Pt, Pd, Ru, and Au) and was concentrated in the -25 µm fraction. The results of automated mineralogical analysis showed that the sample was composed of the PGE-sulphides group, comprising 63.6 vol%, PGE-sulfarsenides 10.4 vol%, PGE-arsenides 1.3 vol%, PGE-bismuth tellurides 3.3 vol%, PGMs-alloy 4.1 vol%, and Laurite comprising 17.3 vol% of the total PGE population. The sample was composed of 66.5 vol% of liberated PGMs, 0.2 vol% attached to liberated BMS, 27.3 vol% of PGMs attached to or locked within silicate or oxide gangue composite particles, 0.2 vol% of PGMs associated with BMS attached to silicate or oxide gangue particles, and a low proportion (5.8 vol%) of PGMs reported being locked within gangue or oxide particles. The majority of PGM grains observed were reported in the fast-floating category (64.4 vol%), 27.6 vol% in the slow-floating 1 category, 2.2 vol% in the slow-floating 2 category, and 5.8 vol% to the non-floating category. The results of the study revealed that the PGMs of MG 1–4 chromite tailings were liberated; however, the low liberation index (<0.2) suggested that a significant portion of PGMs remained trapped within gangue, hindering their recovery. This highlights the need for effective comminution (crushing and grinding) to achieve better liberation. The sample contained fine particles that were more prone to being lost in the tailings and to lowering recovery due to the slimes coating valuable minerals. The recovery of the PGMs from this complex’s polymetallic bodies of low-grade and complex mineralogy will be insufficient with traditional methods and thus innovation is needed. Innovation like advanced comminution, novel flotation equipment or reagents, selective leaching and bioprocessing can overcome these challenges. Full article

This article compares chemical coagulation with electrocoagulation, two popular methods for the primary treatment of wastewater generated in the process of underground coal gasification (UCG). The primary aim was to determine which method is more effective in the removal of cyanide and sulphide ions, metals and metalloids, as well as organic compounds. In both cases, experiments were conducted in batch 1 dm³ reactors and using iron ions. Four types of coagulants were tested during the chemical coagulation study: FeCl₂, FeSO₄, Fe₂(SO₄)₃, and FeCl₃. In the electrocoagulation experiments, pure iron Armco steel was used to manufacture the sacrificial iron anode. Both processes were tested under a wide range of operating conditions (pH, time, Fe dose) to determine their maximum efficiency for treating UCG wastewater. It was found that, through electrocoagulation, a dose as low as 60 mg Fe/dm³ leads to >60% cyanide reduction and >98% sulphide removal efficiency, while for chemical coagulation, even a dose of 307 mg Fe/dm³ did not achieve more than 24% cyanide ion removal. Moreover, industrial chemical coagulants, especially when used in very high doses, can be a substantial source of cross-contamination with trace elements. Full article

Posidonia oceanica significantly contributes to the health of oceans and coastal areas; however, its progressive decline is becoming an increasing source of concern. The present preliminary study aims to assess the chemical parameters that describe the state of preservation of the aforementioned plant meadows located in the Tremiti Islands archipelago. To better understand the plants’ response to external factors, the emission of biogenic volatile organic compounds (BVOCs) was investigated using Posidonia oceanica as a biological indicator. Subsequently, the heavy metal concentrations (Ag, Al, As, Ba, Be, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sb, Se, Sn, Ti, Tl, V, Zn) in sediments, leaves, and seawater were determined and pollution indicators were calculated to assess the deviation from the natural background levels of sediments. The dimethyl sulfoniopropionate (DMSP) to dimethyl sulfoxide (DMSO) ratio was calculated to evaluate the oxidative stress levels in the meadows because the DMSP naturally present in Posidonia oceanica is oxidized to DMSO and decreases the ratio of DMSP/DMSO. BVOC analysis revealed dimethyl sulphide (DMS) as the most abundant molecule. Morphological features led to variations in metal concentrations across sampling sites, with sheltered bays displaying a higher metal content. Degradation is indicated by a greater DMSO content in the outer leaves. In accordance with the metal content, the bioindicator ratio confirms greater degradation on the south side, which aligns with increased oxidative stress. Full article

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

The study object was slag from the Balkhash copper smelter, obtained by re-melting anode mud containing nonferrous metals. The process flow for processing these slags includes sintering with Na₂SO₄, Na₂CO₃, and coal, followed by soda-alkaline leaching of the sinter and extraction of metals from the solution into marketable products. Since sintering is the main operation providing high selectivity, the composition of the products of this process was studied. The main transformations during sintering were determined, and the optimal parameters were identified. The structures of slags and sintered materials obtained during the experiments were studied by electron-probe microanalysis. Sintering was performed at 600–800 °C. The best results for sulphidization of slag components were obtained at 800 °C; a further increase in temperature leads to the smelting of sinter particles and slows down sulphidization. The optimal quantities of additives, based on the weight of the slag, are Na₂SO₄—45%, Na₂CO₃—15%, and reducing agent—41%, with a sintering time of 2 h. These conditions enable the sulphidization of non-ferrous metals in the slag to the entire depth of the polymetallic globules. The distinct concentration of harmful impurities (Ni, As, and Sb) was observed in the fine structure of the polymetallic globules. Full article

The significance and challenges of hydrotreatment processes for vegetable oils have recently become apparent, encompassing various reactions like decarbonylation, decarboxylation, and hydrogenation. Heterogeneous noble or transition metal catalysts play a crucial role in these reactions, offering high selectivity in removing oxygen and yielding desired hydrocarbons. Notably, both sulphided and non-sulphided catalysts exhibit effectiveness, with the latter gaining attention due to health and toxicity concerns associated with sulphiding agents. Nickel-based catalysts, such as NiP and NiC, demonstrate specific properties and tendencies in deoxygenation reactions, while palladium supported on activated carbon catalysts shows superior activity in hydrodeoxygenation. Comparisons between the performances of different catalysts in various hydrotreatment processes underscore the need for tailored approaches. Transition metal phosphides (TMP) emerge as promising catalysts due to their cost-effectiveness and environmental friendliness. Ultimately, there is an ongoing pursuit of efficient catalysts and the importance of further advancements in catalysis for the future of vegetable oil hydrotreatment. Full article

This review details both the conventional and emerging methods of extracting tin from cassiterite. The emerging methods reviewed include sulphuric acid leaching of SnO, cooling crystallization of SnO, sulphide leaching, alkaline leaching, and dry chlorination. From these methods, the conventional approach (direct reduction smelting) stands out as the sole method that is suitable for industrial application, with none of the emerging ones being promising enough to be a contender. The thermodynamics involved in the hydrometallurgical extraction of tin from the mineral are also discussed. ${\Delta G}^o$ values calculated at 25 °C for the reduction–dissolution of SnO₂ using reducing gases revealed feasibility only when carbon monoxide was used. An indication of the possible species produced during the hydrolysis of the oxide of the metal (SnO₂ and SnO) as a function of pH (ranging from −2 to 14 and 0 to 14 for SnO₂ and SnO, respectively) was noted and highlighted to link a Pourbaix diagram generated from literature data. This diagram suggests that the solubility of SnO₂ in both strongly acidic and alkaline media is possible, but with a small dissolution window in each. The purification and recovery routes of the various processing techniques were then envisaged. Full article

Purifying biogas can enhance the performance of distributed smart grid systems while potentially yielding clean feedstock for downstream usage such as steam reforming. Recently, a novel anion-pillared metal–organic framework (MOF) was reported in the literature that shows good capacity to separate acetylene from carbon dioxide. The present study assesses the usefulness of this adsorbent for separating a typical biogas mixture (consisting of methane, nitrogen, oxygen, hydrogen, carbon dioxide, and hydrogen sulphide) using a multiscale approach. This approach couples atomistic Monte Carlo simulations in the grand canonical ensemble with the batch equilibrium modelling of a pressure swing adsorption system. The metal–organic framework displays selectivity at low pressures for carbon dioxide and especially hydrogen sulphide. An analysis of adsorption isotherm models coupled with statistical distributions of surface–gas interaction energies determined that both CH₄ and CO₂ exhibited Langmuir-type adsorption, while H₂S displayed Langmuir-type behaviour at low pressures, with increasing adsorption site heterogeneity at high pressures. Batch equilibrium modelling of a vacuum swing adsorption system to purify a CH₄/CO₂ feedstock demonstrated that such a system can be incorporated into a solar biogas reforming process since the target purity of 93–94 mol-% methane for incorporation into the process was readily achievable. Full article

This study aimed at determining the concentration and possibility of migration of potentially harmful elements (PHEs) in soils and mining and metallurgical waste in the Silesian-Cracow region. Our research was carried out in selected locations of Ruda Śląska, Świętochłowice, Bytom, and in the Olkusz region (Bukowno) in southern Poland. The concentrations of metals (e.g., Ag, Ba, Ca, Cd, Cu, Fe, Mg, Mn, Pb, Sr, Zn), metalloids (As, Sb), and sulphur were determined in 33 soil samples (with a depth range of 0.0–0.3 m) and 12 slag samples. These studies show an increased concentration of metals, metalloids, and sulphur, exceeding the level of regional geochemical background. The research results indicate that the degree of the chemical transformation of soils in the analysed regions of Ruda Śląska, Bytom, and Bukowno is advanced. This highlights the high concentrations of most metals, i.e., arsenic, antimony, and sulphur, in the surface layer of soils (topsoil) due to historic Zn-Pb ore mining and Zn and Fe metallurgy. The presence of both primary and secondary metal sulphides, sulphates, carbonates, oxides/hydroxides, silicates, and aluminosilicates was found in the mineral composition of soils and slags. Full article