Immobilization Of Heavy Metals Research Articles

Production, characterization and environmental remediation application of emerging phosphorus-rich biochar/hydrochar: a comprehensive review.

Owing to the high carbon and phosphorus contents, large specific surface area and slow P release capacity of P-rich biochar/hydrochar (CHAR), its application in aquatic (or soil) environments and positive effects on heavy metal (HM) adsorption (or immobilization) have drawn global attention. To provide an overall picture of P-rich CHAR, this review includes a systematic analysis of the current knowledge on the preparation methods, characterization techniques, influencing factors and environmental applications of P-rich CHAR reported in the last ten years. The key findings and recommendations from this review are as follows: (1) there is still a knowledge gap concerning the regulatory mechanism of the key active components of P-rich CHAR at the molecular level. The dominant factors influencing these active components should be elucidated. (2) P-rich CHAR has a high capacity to immobilize most HMs (e.g., Cd, Cu, and Pb). However, it performs poorly with several HMs (e.g., As). Future studies should focus on the interactions between P-rich CHAR and HMs found in soil/water. (3) To meet the long-term requirements for plant growth, more attention should be given to improving the slow-release capacity and utilization efficiency of available P. (4) There is a potential risk of P loss (or eutrophication) due to rainfall and runoff, although P-rich CHAR exhibits excellent performance in terms of HM immobilization and carbon retention. Several reasonable suggestions are provided to solve these problems. In summary, P-rich CHAR has promising prospects in environmental remediation if these shortcomings are overcome.

Clay mineral as catalysis for controlling the nitrogen containing pollutants during sewage sludge pyrolysis

Pyrolysis technology is considered one of the most promising processes for the environmentally friendly disposal of sewage sludge (SS), as it can neutralize pathogens, reduce hazardous substances, and promote the immobilization of heavy metals. However, nitrogen-containing gases produced in SS pyrolysis can be converted to nitrogen oxides, causing serious environmental pollution. In this study, we investigated the evolution of the nitrogen (N) element in rapid pyrolysis of SS and explored the effect of clay minerals (attapulgite, montmorillonite, and kaolin) in regulating N conversion. The results showed that the higher temperature (800 °C) could promote the conversion of pyrroles/pyridines and NOx precursors in char to N2 (the conversion rate was 32.76 %), and clay minerals catalyzed the cleavage of N-containing macromolecules in the bio-oil, reducing the N content in bio-oil from 28.70 % to 6.23 %, and was conducted to realize the denitrification of bio-oil. Notably, the attapulgite (ATP) on N migration was more effective and could reduce the yield of NOx precursors from 23.80 % to 10.55 % by capturing NH4* and inhibiting the secondary reaction, while catalyzing the removal of N2 from pyridine/pyrrole (N2 production increased to 34.38 %). MgO and CaO in the clays played a major role in facilitating the conversion of char-N to N2, and clay structures loading on the biochar surface promoted the catalysis of N-containing volatiles to N2 by metal oxides. This study provides a viable and harmless approach to SS minimization.

Effect of different calcium salts on phosphorus availability and immobilization of heavy metals in municipal sludge derived biochar

Transforming municipal sludge (MS) into biochar via co-pyrolysis with calcium salts enhances phosphorus (P) recovery and reduces the risk of heavy metal contamination. In this study, the performance and mechanism of bioavailable P conversion and heavy metal stabilization were systematically compared under co-pyrolysis of MS with CaCO3, CaO, and CaCl2 at mass ratios of 2.5–10 % at 700 °C. The results showed that CaCl2 had the best ability to convert P from non-apatite inorganic P to apatite P, followed by CaO and then CaCO3. CaO and CaCO3 addition induced more Ca5(PO4)3OH formation, while CaCl2 induced more Ca2PO4Cl and Ca5(PO4)3Cl formation. The degree of stabilization of heavy metals (e.g., Cd, Cr, Cu, Ni, Pd, and Zn) was significantly improved after co-pyrolysis of MS with these salts, thus reducing the potential environmental risk. In particular, because of the dual action mechanism of chloride ions and calcium ions, co-pyrolysis with CaCl2 exhibited the lowest risk of heavy metal contamination compared with CaCO3 and CaO. These findings suggest that addition of 2.5 % CaCl2 can optimize the production of bioavailable P and the stabilization of heavy metals in biochar. This treatment is recommended for the safe utilization of P resources derived via MS pyrolysis.

The competitive and selective adsorption of heavy metals by struvite in the Pb(II)-Cd(II)-Zn(II) composite system and its environmental significance

The prevalence of struvite and other phosphate minerals in eutrophic environments has a significant effect on the transport and transformation of environmental heavy metals, but their competitive immobilization characteristics and mechanisms for heavy metals remain unclear. Three different sources of struvite (BS, CSHS, and CSS) were obtained respectively by biosynthesis and chemical synthesis with or without humic acid to investigate their competitive immobilization characteristics and mechanism of heavy metals in the Pb(II)-Cd(II)-Zn(II) composite system. The results showed that the immobilization of heavy metals by struvite is physico-chemical adsorption and the affinity (in descending order) is Pb(II) >> Cd(II)/Zn(II). Cd(II) promotes the immobilization of Pb(II)/Zn(II) by BS. The order of the selective strength by struvite for Pb(II) is BS >> CSS ≈ CSHS. The study indicates that the difference between struvite holding heavy metal ions is related to the material composition and heavy metal types, and BS shows best selective immobilization for Pb(II) in the Pb(II)-Cd(II)-Zn(II) composite system. This study provides a theoretical basis for understanding the environmental geochemical role and eco-environmental effects of struvite.

Experimental study on solidification/stabilization of leachate sludge by sulfoaluminate cement and MSWI by-products.

Leachate sludge is generated from the biochemical treatment sludge tank for disposing the leachate from landfill municipal solid waste (MSW). It has the characteristics of high water content and high organic matter content. Sulfoaluminate cement (SAC) is used as the main curing agent, and municipal solid waste incineration (MSWI) by-products are used as auxiliary curing agents to solidify/stabilize the leachate sludge. The influences of SAC content and MSWI by-products content on the strength and solidification mechanism of the leachate sludge are investigated by unconfined compressive strength (UCS) test and micro-observation tests. Moreover, the leaching concentration of heavy metals of the solidified samples is analyzed by leaching toxicity test. The results show that the UCS of the solidified samples increases with an increase in cement content. When the cement content is larger than 20%, the UCS of the solidified samples satisfies the strength requirement of landfill. The enhancing effect of bottom ash on the cement-solidified samples is slight. The fly ash is a good auxiliary curing agent for improving the UCS of cement-solidified samples, and the optimal dosage of fly ash is 5% and 15% for the solidified samples with 10 ~ 30% and 40 ~ 50% cement content, respectively. Ten percent fly ash can replace 10% cement to achieve better solidification effect for the solidified samples. The leaching concentration of heavy metals in the solidified sample with 30%/40% cement and 15% fly ash/bottom ash can satisfy the strength and leaching toxicity requirements of landfill. The immobilization of heavy metal of the cement and MSWI by-products solidified samples is mainly achieved through physical adsorption, physical encapsulation, ion exchange, and chemical precipitation.

Cassava (Manihot esculenta) Yield, Nutrition, and Heavy Metal Bioaccumulation Responses to Circular Economy-Based Innovations in a Mining-Degraded Landscape

Mining operations in Ghana's Forest-Savannah Transition Zone have caused widespread land degradation, jeopardizing ecosystems, food security, and agroecological sustainability. In response, we conducted an experiment to evaluate the effects of biochar and poultry litter amendments on cassava (Manihot esculenta) growth, nutritional quality, and heavy metal accumulation at an illegal mining-degraded site in the Amansie Central District of Ashanti, Ghana. The experiment included five treatments: biochar (10 ton/ha), poultry manure (10 ton/ha), a biochar-poultry manure mix (1:1 ratio, 10 ton/ha each), and two control groups (degraded and forest sites). The combined biochar and poultry manure treatment yielded the highest cassava stover biomass (22.9 ton/ha) during the first year. Nutritional characteristics of cassava such as %carbohydrate, %protein and %total ash tubers were influenced by treatment amendments. Additionally, biochar and poultry manure reduced the accumulation of Arsenic (As) by 168.9% and Lead (Pb) by 149.8% in cassava compared with galamsey soil control. This study showcases a circular economy-based approach that employs locally available resources to restore mining-degraded landscapes and enhance regenerative agricultural practices, reducing waste, bioaccumulation of heavy metals and improving carbon sequestration. Promoting the use of biochar and poultry manure amendments for ecological restoration in mining-degraded areas can contribute to sustainable land use, food security, and livelihoods. Policymakers should consider these strategies to align with global and national development goals while improving food systems and ecosystem services. Future research should explore the long-term impacts of cassava cultivation on amended mining sites and assess the potential of these amendments for agroecological enhancement and heavy metal immobilization.

Recycling of waste glass and incinerated sewage sludge ash in glass-ceramics

Disposal of waste glass and incinerated sewage sludge ash (ISSA) in landfills is a waste of resources and poses significant environmental risks. This work aims to recycle waste glass and ISSA together to form value-added glass-ceramics. The physical and mechanical properties, leaching behaviour, and microstructure of the glass-ceramics produced with different proportions of waste glass powder (WGP) and ISSA were investigated. Thermodynamic calculations were performed to predict the formation of crystalline phases and the phase transformation involved. The results showed the potential of WGP and ISSA as raw materials in glass-ceramics production. WGP effectively densified the microstructure of the glass-ceramics by forming a viscous phase. As WGP content increased, the total porosity of glass-ceramics decreased whereas the density increased, accompanied by the formed anorthite transforming into wollastonite. The incorporation of WGP densified and refined the pore structure of the glass-ceramics, thereby improving the mechanical properties and reducing the water absorption. The glass-ceramics produced with a 50:50 blend of WGP and ISSA exhibited the highest compressive strength of 43.7 MPa and the lowest water absorption of 0.3 %. All fabricated glass-ceramics exhibited innocuous heavy metal leaching. The co-sintering of ISSA and WGP can produce additive-free glass-ceramics, characterized by reduced energy consumption and notable heavy metal immobilization capacity. These materials hold promise for utilization in construction as building materials.

Simultaneous Immobilization of Heavy Metals in MKPC-Based Mortar-Experimental Assessment.

Heavy metal contamination, associated with the increase in industrial production and the development of the population in general, poses a significant risk in terms of the contamination of soil, water, and, consequently, industrial plants and human health. The presence of ecotoxic heavy metals (HMs) thus significantly limits the sustainable development of society and contributes to the deterioration of the quality of the environment as a whole. For this reason, the stabilization and immobilization of heavy metals is a very topical issue. This paper deals with the possibility of the simultaneous immobilization of heavy metals (Ba2+, Pb2+, and Zn2+) in mortar based on magnesium potassium phosphate cement (MKPC). The structural, mechanical, and hygric parameters of mortars artificially contaminated with heavy metals in the form of salt solutions were investigated together with the formed hydration products. In the leachates of the prepared samples, the content of HMs was measured and the immobilization ratio of each HM was determined. The immobilization rate of all the investigated HMs was >98.7%, which gave information about the effectiveness of the MKPC-based matrix for HM stabilization. Furthermore, the content of HMs in the leachates was below the prescribed limits for non-hazardous waste that can be safely treated without any environmental risks. Although the presence of heavy metals led to a reduction in the strength of the prepared mortar (46.5% and 57.3% in compressive and flexural strength, respectively), its mechanical resistance remained high enough for many construction applications. Moreover, the low values of the parameters characterizing the water transport (water absorption coefficient Aw = 4.26 × 10-3 kg·m-2·s-1/2 and sorptivity S = 4.0 × 10-6 m·s-1/2) clearly demonstrate the limited possibility of the leaching of heavy metals from the MKPC matrix structure.

Insights into the interaction between mineral formation and heavy metals immobilization, mediated by Virgibacillus exopolymeric substances

Heavy metal pollution poses significant risks to both the environment and human health due to their toxicity, long residence times, and their ability to bioaccumulate and bio magnify across the food chain. To address this issue, microbial biomineralization has emerged as a promising approach to the bio-removal of heavy metals through immobilization. This process is facilitated by extracellular polymeric substances (EPS), which also play a crucial role in mediating mineral formation. In this study, the interactions between several selected heavy metals (Cd2+, Cu2+, Ni2+, Zn2+), EPS, and mineral formation were investigated using two mineral-forming Virgibacillus strains isolated from the Qatari sabkhas, which are known to be suitable sites for the formation of biominerals. An additional non-mineral-forming Virgibacillus strain isolated from the Dukhan oil waste dumpsite was also investigated. Cd2+ and Zn2+ were to inhibit mineral formation, likely due to competition with Ca2+ and Mg2+ ions during biomineralization. However, exposure to Ni2+ or Cu2+ resulted in changes in the FTIR spectra of the EPS, suggesting the presence of specific functional group bindings within the EPS matrix. The EPS produced by each strain was also directly associated with their efficiency (%) at removing heavy metals. Notably, the EPS from Virgibacillus halodenitrificans Z4D1, the non-mineral-forming strain, exhibited the highest heavy metal removal efficiency of 31.7 % for Zn2+. These findings reveal that EPS do not only affect the biomineralization process but also that the functional groups in EPS have a direct effect on the immobilization of several heavy metals. Conditions that are not suitable for mineral formation may instead be appropriate for the removal of specific heavy metals.

Influence of Enriched Urease Producing Bacteria from Leachate and Restaurant Wastewater on Heavy Metal Removal

The escalation of heavy metal pollution in natural ecosystems due to industrialization presents a critical environmental concern, endangering the well-being of living organisms. Microbially Induced Carbonate Precipitation (MICP) technology, an emerging innovation, has gained attention from the scientific community for its potential in biocementation and bioremediation applications. However, a substantial gap in understanding exists regarding the utilization of ureolytic microbial strains from waste sources capable of effectively immobilizing high concentrations of heavy metals. This study endeavors to explore the latent potential of indigenous ureolytic bacteria derived from leachate and restaurant wastewater, possessing bioremediation capabilities for heavy metal immobilization. The investigation includes microbial screening, physiological characterization of ureolytic bacteria, assessment of their tolerance levels, and evaluation of heavy metal removal efficacy through Atomic Absorption Spectrophotometry (AAS) analysis. Notably, the results reveal that ureolytic bacteria from restaurant wastewater are more tolerant to Cd2+ concentrations compared to their leachate counterparts, manifesting optimum conductivity, pH, and optical density (OD). More so, AAS analysis demonstrates the restaurant wastewater-derived sample's remarkable proficiency in Cd2+ removal, achieving a substantial 95% removal rate, significantly outperforming the leachate wastewater sample's removal rate of 53%.

A comprehensive study of artificial neural network for sensitivity analysis and hazardous elements sorption predictions via bone char for wastewater treatment

Using bone char for contaminated wastewater treatment and soil remediation is an intriguing approach to environmental management and an environmentally friendly way of recycling waste. The bone char remediation strategy for heavy metal-polluted wastewater was primarily affected by bone char characteristics, factors of solution, and heavy metal (HM) chemistry. Therefore, the optimal parameters of HM sorption by bone char depend on the research being performed. Regarding enhancing HM immobilization by bone char, a generic strategy for determining optimal parameters and predicting outcomes is crucial. The primary objective of this research was to employ artificial neural network (ANN) technology to determine the optimal parameters via sensitivity analysis and to predict objective function through simulation. Sensitivity analysis found that for multi-metals sorption (Cd, Ni, and Zn), the order of significance for pyrolysis parameters was reaction temperature > heating rate > residence time. The primary variables for single metal sorption were solution pH, HM concentration, and pyrolysis temperature. Regarding binary sorption, the incubation parameters were evaluated in the following order: HM concentrations > solution pH > bone char mass > incubation duration. This approach can be used for further experiment design and improve the immobilization of HM by bone char for water remediation.

Sustainable Alkali-Activated Mortars for the Immobilization of Heavy Metals from Copper Mine Tailings

Sustainable Alkali-Activated Mortars for the Immobilization of Heavy Metals from Copper Mine Tailings

Rare Earth Elements Recovery and Waste Management of Municipal Solid Waste Incineration Ash.

The advancements in high-tech products and pursuit of renewable energy demand a massive and continuously growing supply of rare earth elements (REE). However, REE production from mining is heavily restricted by technoeconomic limitations and global geopolitical tensions. Municipal solid waste incineration ash (MSWIA) has been recently recognized as a potential alternative for REE recovery. This study applies and optimizes a green modular treatment system using organic ligands for effective REE recovery and concentration from MSWIA with minimal generation of secondary wastes. Citrate extracted >80% of total REE at pH 2.0 and ∼60% at pH 4.0. A subsequent oxalate precipitation step selectively concentrated >98% of extracted REE by ∼7-12 times compared to raw MSWIA. Waste byproducts were upcycled to synthesize zeolites, resulting in an overall solid waste volume reduction of ∼80% and heavy metal immobilization efficiency of ∼75% with negligible leaching, bringing the dual benefits of REE recovery and waste management. This work serves as a pioneer study in REE recovery from an emerging source and provides system level insights on the practicality of a simple three-step treatment system. Compared to existing literature, this system features a low chemical/energy input and a light environmental footprint.

Simultaneous immobilization of multiple heavy metal(loid)s in contaminated water and alkaline soil inoculated Fe/Mn oxidizing bacterium

Two strains of Fe/Mn oxidizing bacteria tolerant to high concentrations of multiple heavy metal(loid)s and efficient decontamination for them were screened. The surface of the bio-Fe/Mn oxides produced by the oxidation of Fe(II) and Mn(II) by Pseudomonas taiwanensis (marked as P4) and Pseudomonas plecoglossicida (marked as G1) contains rich reactive oxygen functional groups, which play critical roles in the removal efficiency and immobilization of heavy metal(loid)s in co-contamination system. The isolated strains P4 and G1 can grow well in the following environments: pH 5-9, NaCl 0-4%, and temperature 20-30°C. The removal efficiencies of Fe, Pb, As, Zn, Cd, Cu, and Mn are effective after inoculation of the strains P4 and G1 in the simulated water system (the initial concentrations of heavy metal(loid) were 1 mg/L), approximately reaching 96%, 92%, 85%, 67%, 70%, 54% and 15%, respectively. The exchangeable and carbonate bound As, Cd, Pb and Cu are more inclined to convert to the Fe-Mn oxide bound fractions in P4 and G1 treated soil, thereby reducing the phytoavailability and bioaccessible of heavy metal(loid)s. This research provides alternatives method to treat water and soil containing high concentrations of multi-heavy metal(loid)s.

Alkali-activated geopolymer materials prepared from coal gangue and municipal solid waste incineration byproducts

Coal gangue and municipal solid waste incineration byproducts (fly ash and bottom ash) are considered as solid and hazardous waste, respectively, and the accumulation of these wastes leads to significant environmental issues. Coal gangue is rich in Si and Al but lacks of Ca, making it challenging to create alkali-activated cementitious materials with good mechanical performances. Fly ash and bottom ash are abundant in Ca. The feasibility of using fly ash and bottom ash as calcium sources for preparing alkali-activated coal gangue-based geopolymers is investigated in the present work. The unconfined compressive strength (UCS) test and microscopic tests (XRD, FTIR, TGA, SEM and ICP-OES) are conducted to study the strength and reaction mechanism of coal gangue and fly ash/bottom ash (CGFA/BA) geopolymers. The results show that the strength of CGFA/BA geopolymers initially increases and then decreases with an increase in fly ash and bottom ash content, and the optimal dosage of fly ash and bottom ash is 15% and 30%, respectively. The liquid-solid ratio and alkali solution (NaOH/Na2SiO3) ratio have a significant influence on the strength of the CGFA/BA geopolymers and the optimal alkali solution ratio is 25:75, while the liquid-solid ratio of 0.45 and 0.60 is recommended for CGFA and CGBA geopolymers, respectively. The CGFA geopolymer with 15% fly ash, 25:75 alkali solution ratio, 0.45 liquid–solid ratio and 8 mol/L sodium hydroxide concentration obtains the highest UCS of 30.28 Mpa. The heavy metal immobilization efficiency (IE) of the CGFA geopolymer is better than that of the CGBA geopolymer. The IE of heavy metals of the CGFA geopolymer is larger than 84.66% and that of the CGFA geopolymer is larger than 55.95%. In the CGFA geopolymer, the IE is Hg>Pb>Zn>Cd>Cr>Ba, while in the CGBA geopolymer, the IE is Hg>Cd>Ba>Cr>Zn>Pb.

Synthesis of tailing slurry-based geopolymers for the highly efficient immobilization of heavy metals: Behavior and mechanism

This study utilized an untreated bauxite tailing (BT) slurry to synthesize geopolymers to reduce material drying and calcination costs and achieve resource utilization of the BT slurry. The effects of BT content, liquid-to-solid (L/S) ratio, sodium silicate modulus, and concentration on compressive strength were analyzed, along with the geopolymer's resistance to water-induced erosion and its ability to immobilize Pb2+ and Cu2+. The results demonstrated that increasing BT content resulted in a decrease in compressive strength, but the complete substitution of fly ash (FA) with BT slurry resulted in a 28 d compressive strength of 4.89 MPa. Although BT slurry-based geopolymers (BTGs) had good resistance to water-induced in stability because of their dense structure, the addition of heavy metals weakened their mechanical strength. Leaching tests showed that the BTGs had an immobilization efficiency of greater than 96.5% for Pb2+ and between 93% and 96% for Cu2+ in landfill leachate, and all immobilization efficiencies for heavy metals in acid rain leachate exceeded 99.9%. The outcomes of characterization studies revealed that Pb2+ and Cu2+ engaged in geopolymerization and immobilized through the chemical bonding of T (Si, Al) − O − M (Pb, Cu) and physical sealing. This study presents a low-energy-consumption technology that effectively enhances the utilization of BT slurry. In situ material extraction can be used to remediate contaminated soils in tailing pond areas.

Codisposal of landfill leachate concentrate and antimony mine soils using a one-part geopolymer system for cationic and anionic heavy metals immobilization

Geopolymer solidification/stabilization technology has developed rapidly in the remediation field of heavy metal-contaminated soil. However, geopolymers exhibit low anionic heavy metal immobilization efficiency due to their electronegativity and alkali activation characteristics. This study constructed a one-part blast furnace slag-based geopolymer system using landfill leachate concentrate (LLC) as chlorine and humic acid sources and achieved the solidification/stabilization of cations (Cd, Cu, Hg, and Pb) and anions (Sb and As) in the antimony mine soils (AMS). The LLC addition increased the Sb and As fixation rates from 92%∼94% and 82∼86%, respectively, to over 99%, reducing the leaching concentration of all heavy metal ions to the ppb level. LLC improved the chemical stability and physical encapsulation of Sb/As in three ways: inducing a Friedel’s salt (FS) formation, enhancing humic acid complexation/chelation, and promoting geopolymerization. Wet curing was more conducive to FS formation in the geopolymer than dry curing and increased the 28-day compressive strength by 38.5%. Due to the SiO2 skeleton support effect in AMS, a 30 wt% AMS addition was beneficial for geopolymer strength development. Our study provided a harmless method for the codisposal of LLC and AMS and improved the efficiency of geopolymer fixation of complex heavy metal cations and anions.

Assessment of iron and heavy metals accumulation in the soils of the combat zone

The object of the study is soils in areas with active military operations. The study is dedicated to assessing the environmental impact of military operations through forecasting. The paper highlights the impact of military conflict on the distribution of heavy metals in soils. An analysis of the distribution and interaction of heavy metals in soil is carried out, which helps to understand the dynamics of pollution in the context of military conflict, and allows to understand the complex processes of the impact of military operations on the environment and the state of soil resources. The complex interrelationships between military operations and environmental pollution are revealed, with an emphasis on the importance of studying the distribution and immobilization of iron and heavy metals in the current conditions of the risk of military operations. It is shown that the most rapidly distributed metals in the soil are: iron (Fe), zinc (Zn), cadmium (Cd), antimony (Sb); the slowest: arsenic (As), lead (Pb), copper (Cu), nickel (Ni), mercury (Hg), manganese (Mn), vanadium (V). It was found that loams and chernozems are more prone to the accumulation of heavy metals and iron than sandy soils. Compared to sandy soil, the rate of metal release in loam decreases from 16.7 % to 69.7 %. In comparison of chernozem to loam, the release rate slows down from 17.85 % to 32.08 %. It was found that the rate of spreading of barium, cobalt, arsenic, lead, mercury, manganese, strontium and titanium does not depend on the type and mechanical parameters of the soil. The practical use of the results will help to predict the mechanism of pollution spread and help to identify the highest risk areas. The results of the study indicate the need to develop scientifically sound strategies for environmental protection and promotion of sustainable development in the area affected by military events

Co-treatment of steel slag and oil shale waste in cemented paste backfill: Evaluation of fresh properties, microstructure, and heavy metals immobilization

The environmentally sustainable treatment of steel slag (SS) and oil shale waste (OSW) is a significant concern in the field of industrial development. The mining industry also faces challenges related to the high costs and carbon emissions associated with ordinary Portland cement (OPC), leading to environmental pollution. To address these challenges, this study aimed to develop a cost-effective and environmentally friendly binder for cemented paste backfill (CPB) by utilizing SS and calcined oil shale waste (COSW) as primary precursors. Extensive investigations were conducted to evaluate the properties of the CPB sample with varying COSW content, including rheological properties, mechanical strength, and microstructure. The binder sample was comprehensively characterized using isothermal calorimetric analysis, X-ray diffraction (XRD), thermogravimetry (TG), and scanning electron microscopy (SEM). Based on systematic experimentation, an optimal blend ratio for the binder was determined, consisting of 60 wt% SS, 15 wt% COSW, 15 wt% phosphogypsum (PG), and 10 wt% OPC. The exceptional performance of the binder was attributed to the substantial formation of precipitated ettringite (AFt), resulting in a more compact structure and improved mechanical strength. Additionally, a sequential extraction test revealed that the heavy metals in the CPB sample were mainly present in the residual fraction, demonstrating the effective immobilization of heavy metals by the binder.

Source control on the acid mine drainage produced by the oxidation of pyrite and sulfur-containing uranium tailings based on the microbially induced carbonate precipitation technology

Large quantities of acid mine drainage (AMD) generated through the oxidation of sulfide-bearing minerals, particularly pyrite, pose a significant global environmental challenge. The implementation of efficient and fundamental governance methods is crucial as current conventional approaches fail to address the root cause of this problem. To investigate the technique of controlling AMD at its source, a 10-day static experiment was conducted in order to examine the inhibitory effect of Sporosarcina pasteurii (S. pasteurii) on oxidative acid production from pyrite under varying redox potentials (Eh) and Ca2+ concentrations. Additionally, a 180-day dynamic column experiment was carried out to assess the long-term stability of its inhibition and heavy metal fixation. The results of both short-term and long-term analysis indicate that the metabolic activity of S. pasteurii has beneficial effects on the control of AMD through sulfur oxidation, even in the presence of strong oxidants such as H2O2 and FeCl3. 1. It stabilizes pH within the neutral to alkaline range; 2. It maintains Eh at a low potential reducing environment; 3. It promotes an increase in SO42− concentration, followed by a decline and stabilization at lower concentrations; 4. It supplies carbonate for pyrite oxidation, maintaining a balance between acid production and consumption. Additionally, SEM, XRD, and XPS results demonstrated that the mineral surface appeared flat without prominent characteristic peaks of oxidation products, indicating effective inhibition of pyrite oxidation by S. pasteurii. The immobilization experiments for heavy metals showed that Cd exhibited the highest fixation effect with a rate of 94%; Mn, Cu, Zn, and Co had the second best fixation effect with ion concentrations decreasing by 82%, 83%, 87%, and 88% respectively; Ni and U(VI) decreased by rates of 75% and 69% respectively. These experimental findings suggest that S.pasteurii can effectively inhibit pyrite oxidation as well as sulfur-containing uranium waste rock oxidation while providing long-term stabilization for heavy metal immobilization.