Mesoporous Silica MCM-41 from Fly Ash as a Support of Bimetallic Cu/Mn Catalysts for Toluene Combustion.

The main outcome of this research was to demonstrate the opportunity to obtain a stable and well-ordered structure of MCM-41 synthesized from fly ash. A series of bimetallic (Cu/Mn) catalysts supported at MCM-41 were prepared via grinding method and investigated in catalytic toluene combustion reaction to show the material's potential application. It was proved, that the Cu/Mn ratio had a crucial effect on the catalytic activity of prepared materials. The best catalytic performance was achieved with sample Cu/Mn(2.5/2.5), for which the temperature of 50% toluene conversion was found to be 300 °C. This value remains in line with the literature reports, for which comparable catalytic activity was attained for 3-fold higher metal loadings. Time-on-stream experiment proved the thermal stability of the investigated catalyst Cu/Mn(2.5/2.5). The obtained results bring a valuable background in the field of fly ash utilization, where fly ash-derived MCM-41 can be considered as efficient and stable support for dispersion of active phase for catalyst preparation.

Feroxyhyte - from synthesis and characterization to application.

Feroxyhyte (δ-FeOOH) was synthesized and characterized using X-ray diffractometry (XRD), simultaneous thermal analysis (STA), scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDS), and low-temperature nitrogen adsorption-desorption measurements. Its potential application as adsorbent of an anionic and cationic dyes such as C.I. Acid Violet 1 (AV1) and C.I. Basic Blue 3 (BB3) was investigated by determining the adsorption capacities based on the Langmuir (36.6 mg/g for AV1 and 187 mg/g for BB3), Freundlich and Dubinin-Radushkevich isotherm models. Adsorption of AV1 and BB3 by δ-FeOOH drops with the presence of additives such as cationic and anionic surfactants (CTAB, SDS) and ionic polymers (PAA, PEI). The surface and electrokinetic properties of examined suspensions were also described. They include determination of the solid surface charge density and the zeta potential, as well as values of point of zero charge and isoelectric point of feroxyhyte particles without and with adsorbed layers of organic substances. Their analysis made possible to propose the most probable structure of electrical double layer formed at the iron mineral/aqueous solution interface.

Comparison of pesticide adsorption efficiencies of zeolites and zeolite-carbon composites and their regeneration possibilities.

The presence of pesticides in our environment is a consequence of intensive industrial and civilizational development, necessitating the search for effective and safe methods to remove them. We suggest utilizing zeolite X and a zeolite-carbon composite, obtained through the chemical transformation of fly ash, as pesticide sorbents. To increase the sorption efficiency of 2,4-dichlorophenoxyacetic acid (2,4-D), 2-methyl-4-chlorophenoxyacetic acid (MCPA), carbendazim, and simazine, we functionalized the zeolite materials with cationic (hexadecyltrimethylammonium) and nonionic (Triton X-100) surfactants. We used transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric/differential thermal analysis (TG/DTA) and point of zero charge (pHpzc) analysis to characterize the functionalized sorbent materials. Our results indicate that cationic surfactants significantly enhance the adsorption of 2,4-D and MCPA. In contrast, carbendazim and simazine exhibit maximum sorption on the unmodified zeolite-carbon composite. The sorption mechanism is intricate, with physical sorption predominating, primarily due to electrostatic interactions between the protonated binding sites of the adsorbents and the negatively charged pesticide molecules. Regeneration tests demonstrated that ethanol is the most effective in regenerating zeolite-carbon composite with adsorbed MCPA and 2,4-D, while thermal regeneration was not possible. Adsorbents with simazine and carbendazim can be regenerated using both thermal and ethanol methods, but the thermal regeneration of zeolite with adsorbed simazine is more efficient. Utilizing functionalized zeolite materials obtained from industrial waste, such as fly ash, could provide an efficient way to remove pesticides from the environment.

Modified Natural Diatomite with Various Additives and Its Environmental Potential.

Diatomite has recently been the subject of intensive scientific research aimed at its extensive use in industry, breeding and agriculture. The only active diatomite mine is in Jawornik Ruski, in the Podkarpacie region of Poland. Chemical pollution in the environment, including that from heavy metals, poses a threat to living organisms. Reducing the mobility of heavy metals in the environment through the use of diatomite (DT) has recently gained much interest. More effective immobilisation of heavy metals in the environment with DT, mainly through the modification of its physical and chemical properties by various methods, should be applied. The aim of this research was to develop a simple and inexpensive material showing more favourable chemical and physical properties compared with unenriched DT in terms of metal immobilisation. Diatomite (DT), after calcination, was used in the study, considering three grain fractions, i.e., 0-1 mm (DT1); 0-0.5 mm (DT2) and 5-100 µm (DT3). Biochar (BC), dolomite (DL) and bentonite (BN) were used as additives. The proportion of DTs in the mixtures amounted to 75%, and of the additive, 25%. The use of unenriched DTs after calcination poses the risk of releasing heavy metals into the environment. Enrichment of the DTs with BC and DL resulted in a reduction or absence of Cd, Zn, Pb and Ni in aqueous extracts. It was found that for the specific surface area values obtained, the additive used for the DTs was of crucial importance. The reduction in DT toxicity has been proven under the influence of various additives. The mixtures of the DTs with DL and BN had the least toxicity. The obtained results have economic importance, as the production of the best quality sorbents from locally available raw materials reduces transport costs and thus the environmental impact. In addition, the production of highly efficient sorbents reduces the consumption of critical raw materials. It is estimated that the savings from producing sorbents with the parameters described in the article can be significant in comparison with popular competitive materials of other origins.

Infrared spectroscopy: the key to elucidating the sorption mechanism of surfactants, dyes and pharmaceuticals on mineral composite material.

There is a global problem with the effective purification of wastewater containing organic compounds, including dyes, pharmaceuticals and surfactants. Therefore, technologies for the removal of pollutants are still being explored. One of the promising methods could be the application of mineral sorbent composite based on lignite and bentonite. However, it is crucial to comprehensively recognize the mechanisms responsible for immobilizing organic compounds using mineral composite sorbents. The purpose of this work was to prepare and investigate the sorption mechanism of lignite-bentonite composite (BL) sorbents for the removal of dyes: Rhodamine B (RB), Remazol Brilliant Blue R (RBBR), pharmaceuticals: ibuprofen (IB), sulfamethoxazole (STX) and surfactant sodium dodecylbenzenesulfonate (SDBS). The quantitative sorption results have been performed using the high-performance liquid chromatography (HPLC) method. The application of infrared (IR) spectroscopy method was crucial to describe the sorption mechanism. After completing the sorption test, the spectra for the sorbents revealed bands associated with adsorbed RB, RBBR, IB, STX, and SDBS on the BL sorbent. Because lignite is predominated in BL composite, the sorption capacity and mechanism strictly correspond to its sorption properties rather than to bentonite ones. The spectra results indicate that the physical sorption process related to electrostatic forces, hydrogen bonding, and dispersion interactions are predominantly responsible for the immobilization of organic compounds tested on mineral sorbents. The X-ray diffraction (XRD) results indicate the ion exchange process involved in the case of RB adsorption on the bentonite sample. Nevertheless, the sorption mechanism was complex because of the extensive sorption properties of mineral composite and the different chemical properties of the tested organic compounds. The results of our spectroscopic studies help interpret the sorption mechanisms of organic compounds on mineral materials.

Zeolite Composite Materials from Fly Ash: An Assessment of Physicochemical and Adsorption Properties.

Waste fly ash, with both low (with the addition of vermiculite) and high contents of unburned coal, were subjected to hydrothermal syntheses aiming to obtain zeolite composite materials-zeolite + vermiculite (NaX-Ver) and zeolite + unburned carbon (NaX-C). The composites were compared with parent zeolite obtained from waste fly ash with a low content of unburned carbon (NaX-FA). In this study, the physicochemical characteristics of the obtained materials were evaluated. The potential application of the investigated zeolites for the adsorption of ammonium ions from aqueous solutions was determined. Composite NaX-Ver and parent zeolite NaX-FA were characterized by comparable adsorption capacities toward ammonium ions of 38.46 and 40.00 mg (NH4+) g-1, respectively. The nearly 2-fold lower adsorption capacity of composite NaX-C (21.05 mg (NH4+) g-1) was probably a result of the lower availability of ion exchange sites within the material. Adsorbents were also regenerated using 1 M NaCl solution at a pH of 10 and subjected to 3 cycles of adsorption-desorption experiments, which proved only a small reduction in adsorption properties. This study follows the current trend of waste utilization (fly ash) and the removal of pollutants from aqueous solutions with respect to their reuse, which remains in line with the goals of the circular economy.

Surface modification of magnetic nanoparticles by bacteriophages and ionic liquids precursors.

Magnetic nanoparticles (MNPs) have recently been a point of interest for many researchers due to their properties. However, the studies on the influence of bacteriophages on the synthesis of MNPs seem to be lacking. Furthermore, bacteriophage-modified MNPs have not been combined with n-alkyl quaternary ammonium ionic liquid precursors (QAS). In this study, the aim was to assess the influence of two distinctly different bacteriophages (Escherichia phage P1 and Pseudomonas phage Φ6) on MNPs synthesis in the presence or absence of QAS. Synthesized MNPs have been characterized with X-ray diffraction (XRD) and Mössbauer spectroscopy in terms of changes in the crystallographic structure; scanning electron microscopy (SEM) for changes in the morphology; and ζ-potential. Moreover, the sorption parameters and the loss of viability of bacteria that interacted with MNPs have been determined. The sorption of bacteria differs significantly among the tested samples. Furthermore, the viability of the bacteria adsorbed on MNPs varies in the presence of QAS, depending on the length of the n-alkyl chain. The study has revealed that MNPs can be bound with bacteriophages. Mössbauer spectroscopy has also revealed the probable influence of bacteriophages on the formation of crystals. However, these phenomena require further studies.

Erythromycin Scavenging from Aqueous Solutions by Zeolitic Materials Derived from Fly Ash.

Erythromycin (EA) is an antibiotic whose concentration in water and wastewater has been reported to be above the standard levels. Since the methods used so far to remove EA from aquatic environments have not been effective, the development of effective methods for EA removal is necessary. In the present study, fly ash (FA)-based zeolite materials, which have not been investigated as EA sorbents before, were used. The possibilities of managing waste FA and using its transformation products for EA sorption were presented. The efficiency of EA removal from experimental solutions and real wastewater was evaluated. In addition, the sorbents' mineral composition, chemical composition, and physicochemical properties and the effects of adsorbent mass, contact time, initial EA concentration, and pH on EA removal were analyzed. The EA was removed within the first 2 min of the reaction with an efficiency of 99% from experimental solutions and 94% from real wastewater. The maximum adsorption capacities were 314.7 mg g-1 for the fly ash-based synthetic zeolite (NaP1_FA) and 363.0 mg g-1 for the carbon-zeolite composite (NaP1_C). A fivefold regeneration of the NaP1_FA and NaP1_C showed no significant loss of adsorption efficiency. These findings indicate that zeolitic materials effectively remove EA and can be further investigated for removing other pharmaceuticals from water and wastewater.

Functionalised Mineral Materials in Environmental and Civil Engineering, Ceramics, Foundries and Metals.

There has been increasing interest in functionalised mineral materials in terms of both scientific research and the development of the world economy [...].

Surface Modification of Synthetic Zeolites with Ca and HDTMA Compounds with Determination of Their Phytoavailability and Comparison of CEC and AEC Parameters.

Zeolites obtained from fly ash are characterized by very good anion- and cation-exchange properties and a developed porous structure. This paper presents the results of surface modification studies of synthetic zeolites obtained from calcined coal shale (clay materials). Calcium compounds and hexadecyltrimethylammonium bromide (HDTMA) were used as modifying substances. The characteristics of the raw material and the zeolite obtained as a result of its synthesis are presented. The surface modification method is described. Furthermore, the results of sorption and desorption of NO3, PO4, and SO4 from raw and modified samples are presented. The results of anion- and cation-exchange capacities for other zeolite types were also compared. Modification of the materials with Ca ions and HDTMA surfactant only improved the sorption of sulfates. The 90% desorption of nitrates, phosphates, and sulphates from the zeolite material without modification indicates a good release capacity of these compounds and their potential use as fertilizer additives.

An assessment of an ion exchange resin system for the removal and recovery of Ni, Hg, and Cr from wet flue gas desulphurization wastewater-a pilot study.

The paper presents the results of a pilot-scale study investigating the efficiency of an ion exchange resin system in the removal of Ni, Hg, and Cr from flue gas desulphurisation wastewater, in the presence of competitive metals such as Ca, Mg, Al, Fe, and Mn. The core part of the ion exchange installation consisted of two columns that were filled with ion exchange resin with iminodiacetic functional groups (Purolite S930) and one column filled with resin with isothiouronium functional groups (Purolite S920). The results showed that Ni, Hg, and Cr were almost completely removed from the wastewater with nearly 100% efficiency. Purolite S930 almost totally removed Ni, reducing its content from 89.3 ± 35 µg dm-3 to below 0.1 µg dm-3, while Purolite S920 reduced the remaining Cr content from 2.2 ± 0.6 µg dm-3 and most of the Hg content, from 23.5 ± 6.6 µg dm-3 to below 0.1 µg dm-3. The competitive metals Ca, Mg, Mn, and Al showed low affinity to the studied ion exchange resins. The study also assessed speciation of ion forms and sorption mechanisms. Breakthrough curve analysis was also carried out, which revealed that the selectivity sequence of iminodiacetic resin was Ni > Cr > Hg > Fe > Al > Mn > Ca, Mg. Elution studies were performed on S930 resins that allowed the separation of two streams: one containing mostly Ni and Fe which can be subjected to Ni recovery and the other containing mostly Cr and Hg which can be separated.

Immobilization mechanism of Cd2+/HCrO4-/CrO42- ions and carboxin on montmorillonite modified with Rhizobium leguminosarum bv. trifolii exopolysaccharide.

The modification of clay minerals by exopolysaccharides (EPSs) may significantly increase their adsorption capacity. Therefore, this study focused on the impact of the EPS synthesised by the soil bacterium Rhizobium leguminosarum bv. trifolii on the adsorptive features of montmorillonite relative to two heavy metal ions (cadmium/Cd(II) and chromium/Cr(VI)) and a pesticide (carboxin). The characterization of montmorillonite was carried out using various methods: X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy. The adsorption/desorption data were modelled using theoretical equations (Langmuir-Freundlich, Redlich-Peterson, etc.). The obtained results showed that EPS promoted the accumulation of heavy metals on the clay mineral and, simultaneously, contributed to a lower degree of their desorption. This resulted from complexation between the biopolymer and the Cd(II)/Cr(VI) ions. After montmorillonite modification with 100 mg/L EPS, the maximum noted growth in Cd(II) adsorption was 26.10%, whereas it was 20.30% for Cr(VI). The adsorbed amounts of Cd(II) and Cr(VI) were then 24.24 and 14.45 mg/g, respectively. In the case of carboxin, the EPS effect on its adsorption/desorption rates was opposite - its adsorption level decreasing by 10.80%, was 0.27 mg/g. Thus, the presence of EPS-producing bacteria could reduce the bioavailability of the heavy metals, but not of the selected pesticide.

Modified zeolite as a sorbent for removal of contaminants from wet flue gas desulphurization wastewater.

The aim of the present work was to prepare and investigate the sorption efficiency of unwashed cationic surfactant-modified natural zeolite (Cp) for the simultaneous removal of selected inorganic compounds (NH4+, SO42-, NO3-, Fe, Mn, Zn, and Ni) from wet flue gas desulphurization (WFGD) wastewater. The Cp was modified using hexadecyltrimethylammonium bromide (HDTMA-Br) salt in an amount not exceeding its external cation exchange capacity (1.0 ECEC). The present analysis showed that the modification process was completed by forming an incomplete monolayer by the uptaken HDTMA ions. Fourier transform infrared (FTIR) and textural analysis indicated that the adsorbed HDTMA ions formed a disordered, macroporous structure onto Cp surface. Batch adsorption experiments with different sorbent dosages revealed an increase in the sorption efficiency of NH4+ and NO3- with the increase in the amount of modified Cp. The highest removal efficiency was observed at adsorbent dosage of 150 g/L. The studies also revealed, that the SO42- removal did not change significantly regardless the sorbent dosage. The kinetic tests showed that a substantial amount of inorganic compounds was removed within 2 h, and the sorption kinetics of each compound were best fitted to the pseudo-second order model. The studies of adsorption mechanism revealed that cation exchange, anion exchange with Br- counterion, electrostatic interaction between the surfactant and inorganic ions, as well as precipitation of insoluble salts might be involved simultaneously in the immobilization of NH4+, SO42-, NO3-, Fe, Mn, Zn, and Ni.

A Review on the Application of Zeolites and Mesoporous Silica Materials in the Removal of Non-Steroidal Anti-Inflammatory Drugs and Antibiotics from Water.

Zeolites and mesoporous silica materials are effective adsorbents that can be useful for the removal of various pharmaceuticals including non-steroidal anti-inflammatory drugs and antibiotics from low-quality water. This paper summarizes the properties and basic characteristics of zeolites and mesoporous silica materials and reviews the recent studies on the efficacy of the adsorption of selected non-steroidal medicinal products and antibiotics by these adsorbents to assess the potential opportunities and challenges of using them in water treatment. It was found that the adsorption capacity of sorbents with high silica content is related to their surface hydrophobicity (hydrophilicity) and structural features, such as micropore volume and pore size, as well as the properties of the studied medicinal products. This review can be of help to scientists to develop an effective strategy for reducing the amount of these two groups of pharmaceuticals in wastewater.

Removal of Pesticides from Waters by Adsorption: Comparison between Synthetic Zeolites and Mesoporous Silica Materials. A Review.

Pesticides are pollutants found in wastewater due to increasing agricultural activities over the years. Inappropriate dosing of pesticides results in the dispersal of active ingredients in the environment. The complete removal of pesticides from wastewater is an immediate concern due to their high toxicity and mobility. At present, adsorption is one of the most widely used methods for pesticide removal, in which synthetic zeolites and mesoporous silica materials are extensively applied. This article presents a systematic and comparative review of the applications and comparison of these adsorbents, based on the data reported in the literature. The paper summarizes the information collected from various studies, including the type of adsorbents and pesticides used, experimental conditions, and results of each work. The studies analyzed were laboratory-based and show potential advantages for the treatment of pesticide-bearing waters using functionalized and unfunctionalized synthetic zeolites and mesoporous silica materials. As a whole, functionalized materials are reported to exhibit better removal performance for different pesticides than conventional materials. It is expected that the results of this review will help researchers to establish a powerful strategy for the abatement of pesticides in wastewater.

Iron-Based Water Treatment Residuals: Phase, Physicochemical Characterization, and Textural Properties.

Groundwater treatment residuals (GWTRs) are safe waste materials generated during drinking water treatment. GWTRs are mainly deposited in landfills, but the preferred solution should be reused or utilized for some components. To ensure proper sludge management, it is important to provide quality, chemical composition, and texture characteristics of GWTRs. Therefore, in this study, we aimed to investigate and compare the features of GWTRs collected from four water treatment plants. GWTRs were characterized by X-ray diffraction (XRD); scanning electron microscopy (SEM) with energy dispersion spectroscopy (EDS); Fourier transform infrared spectroscopy (FTIR); thermogravimetric, differential thermogravimetric, and differential thermal analysis (TG, DTG, and DTA, respectively); X-ray fluorescence (XRF); inductively coupled plasma optical emission spectrometry (ICP-OEP); specific surface area (SBET) measurement; and determination of the isoelectric point (pHIEP). According to the results, GWTRs are poor crystalline materials that are predominantly composed of ferrihydrite with minor calcite and quartz admixture. They formed heterogeneously mixed particles with irregular shapes. They were mainly composed of iron oxides (32-55%), silica (4-28%), calcium oxide (4-17%), and manganese oxides (0.3-4.0%). They were found to be mesoporous with a large specific surface area. Due to their composition and texture characteristics, GWTRs demonstrate good adsorption properties toward different compounds such as heavy metals and metalloids.

Cavitated Charcoal-An Innovative Method for Affecting the Biochemical Properties of Soil.

Thermal biomass transformation products are considered to be one of the best materials for improving soil properties. The aim of the study was to assess the effect of charcoal after cavitation on the chemical and biochemical properties of soil. The study was carried out with a 10% aqueous charcoal mixture that was introduced into loamy sand and clay at rates of 1.76%, 3.5%, 7.0%, and 14.0%. The effect of the application of cavitated charcoal was tested on Sorghum saccharatum (L.). Soil and plant material was collected to determine chemical and biochemical properties. The application of cavitated charcoal reduced the acidification of both soils. The highest rate (14.0%) of cavitated charcoal increased the content of soil total carbon (CTot) by 197% in the loamy sand compared to CTot in the control treatments, 19% for clay soil, respectively. The application of cavitated charcoal did not significantly change the total content of heavy metals. Regardless of the element and the soil used, the application of cavitated charcoal reduced the content of the CaCl2-extracted forms of heavy metals. Following the application of cavitated charcoal, the loamy sand soil presented an even lower content of the most mobile forms of the studied elements. It should also be noted that regardless of the soil texture, mobile forms of the elements decreased with the increased cavitated charcoal rate. The results of dehydrogenase and urease activity indicated the low metabolic activity of the microbial population in the soils, especially with the relatively high rates (7.0% and 14.0%) of cavitated charcoal. However, the cavitated charcoal used in the study showed a significant, positive effect on the amount of biomass S. saccharatum (L.), and its application significantly reduced the heavy metal content in the biomass of S. saccharatum (L.).

Fundamental features of mesoporous functional materials influencing the efficiency of removal of VOCs from aqueous systems: A review.

Volatile organic compounds (VOCs) are harmful contaminants that are emitted into the environment as a result of various commercial, industrial, and domestic practices. Their presence in water leads to pollution and poses a huge threat to the ecological environment and human health. They are typically released into the environment through a spill or inappropriate disposal which allows the chemicals to get absorbed into the ground or enter the sewage system. Thus far, several treatment methods have been developed to remove VOCs from water, including steam stripping or air stripping, ion exchange, filtration, adsorption, and application of various types of sorbents. Due to their cost-effectiveness and efficiency, the use of mesoporous materials, especially those synthesized from coal fly ash (FA), is recognized as the most promising strategy for slowing down the impact of VOCs. This study is believed to be the first to assess the advances made in improving the adsorption of VOCs by different functional mesoporous materials (FA, zeolites, mesoporous silica, metal organic frameworks). The impact associated with the properties of these materials is carefully summarized in this paper, in regard to their solid-state characteristics, material synthesis method, and surface modification. In addition, their chemical and physical interactions in solution, the reaction kinetics, and the influence of temperature and pH are described in detail. The aim of this work was to compare the sorption properties of the materials synthesized from FA with more complex mesoporous materials. This overview provides a comprehensive understanding of VOC removal from water systems using various functional materials, as well as helps in identifying the materials that may play a key role in the future.

Synthesis and Characterization of Zeolites Produced from Low-Quality Coal Fly Ash and Wet Flue Gas Desulphurization Wastewater.

This study investigated a low-energy-consuming procedure for the synthesis of zeolite materials from coal fly ash (CFA). Materials containing zeolite phases, namely Na-X, Na-P1, and zeolite A, were produced from F-class fly ash, using NaOH dissolved in distilled water or in wastewater obtained from the wet flue gas desulphurization process, under atmospheric pressure at a temperature below 70 °C. The influence of temperature, exposure time, and alkaline solution concentration on the synthesized materials was tested. In addition, chemical, mineralogical, and textural properties of the obtained materials were determined by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), and cation exchange capacity (CEC). Cd(II), Ni(II), NH4+ cation, and Se(VI) anion sorption experiments were conducted to compare the sorption properties of the produced synthetic zeolites with those of the commercially available ones. Zeolitization resulted in an increase of CEC (up to 30 meq/100 g) compared to raw CFA and enhanced the ability of the material to adsorb the chosen ions. The obtained synthetic zeolites showed comparable or greater sorption properties than natural clinoptilolite and synthetic Na-P1. They were also capable of simultaneously removing cationic and anionic compounds. The structural, morphological, and textural properties of the final product indicated that it could potentially be used as an adsorbent for various types of environmental pollutants.

Microbiological Sulfide Removal-From Microorganism Isolation to Treatment of Industrial Effluent.

Management of excessive aqueous sulfide is one of the most significant challenges of treating effluent after biological sulfate reduction for metal recovery from hydrometallurgical leachate. The main objective of this study was to characterize and verify the effectiveness of a sulfide-oxidizing bacterial (SOB) consortium isolated from post-mining wastes for sulfide removal from industrial leachate through elemental sulfur production. The isolated SOB has a complete sulfur-oxidizing metabolic system encoded by sox genes and is dominated by the Arcobacter genus. XRD analysis confirmed the presence of elemental sulfur in the collected sediment during cultivation of the SOB in synthetic medium under controlled physicochemical conditions. The growth yield after three days of cultivation reached ~2.34 gprotein/molsulfid, while approximately 84% of sulfide was transformed into elemental sulfur after 5 days of incubation. Verification of isolated SOB on the industrial effluent confirmed that it can be used for effective sulfide concentration reduction (~100% reduced from the initial 75.3 mg/L), but for complete leachate treatment (acceptable for discharged limits), bioaugmentation with other bacteria is required to ensure adequate reduction of chemical oxygen demand (COD).