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Phosphogypsum (PG) occupies a large amount of land due to its large annual production and low utilization rate, and at the same time causes serious environmental problems due to toxic impurities. PG is used for mine backfill, and industrial solid waste is a curing agent for PG, which can save the filling cost and reduce environmental pollution. In this paper, PG was used as a raw material, combined with steel slag (SS) and ground granulated blast-furnace slag (GGBS) under the action of an alkali-activated agent (NaOH) to prepare all-solid waste phosphogypsum-based backfill material (PBM). The effect of the GGBS to SS ratio on the compressive strength and toxic leaching of PBM was investigated. The chemical composition of the raw materials was obtained by XRF analysis, and the mineral composition and morphology of PBM and its stabilization/curing mechanism against heavy metals were analyzed using XRD and SEM-EDS. The results showed that the best performance of PBM was achieved when the contents of PG, GGBS, and SS were 80%, 13%, and 7%, the liquid-to-solid ratio was 0.4, and the mass concentration of NaOH was 4%, with a strength of 2.8 MPa at 28 days. The leaching concentration of fluorine at 7 days met the standard of groundwater class IV (2 mg/L), and the leaching concentration of phosphorus was detected to be less than 0.001 mg/L, and the leaching concentration of heavy metals met the environmental standard at 14 d. The hydration concentration in PBM met the environmental standard. The hydration products in PBM are mainly ettringite and C-(A)-S-H gel, which can effectively stabilize the heavy metals in PG through chemical precipitation, physical adsorption, and encapsulation. [ABSTRACT FROM AUTHOR]

The routine dredging of waterways produces huge volumes of sediments. Handling contaminated dredged sediments poses significant and diverse challenges around the world. In recent years, novel and sustainable ex situ remediation technologies for contaminated sediments have been developed and applied. This review article focuses on cement-based binders in stabilizing contaminants through the stabilization/solidification (S/S) technique and the utilization of contaminated sediments as a resource. Through S/S techniques, heavy metals can be solidified and stabilized in dense and durable solid matrices, reducing their permeability and restricting their release into the environment. Industrial by-products like red mud (RM), soda residue (SR), pulverized fly ash (PFA), and alkaline granulated blast furnace slag (GGBS) can immobilize heavy metal ions such as lead, zinc, cadmium, copper, and chromium by precipitation. However, in a strong alkali environment, certain heavy metal ions might dissolve again. To address this, immobilization in low pH media can be achieved using materials like GGBS, metakaolin (MK), and incinerated sewage sludge ash (ISSA). Additionally, heavy metals can be also immobilized through the formation of silicate gels and ettringites during pozzolanic reactions by mechanisms such as adsorption, ion exchanges, and encapsulation. It is foreseeable that, in the future, the scientific community will increasingly turn towards multidisciplinary studies on novel materials, also after an evaluation of the effects on long-term heavy metal stabilization. [ABSTRACT FROM AUTHOR]

As industrial production increases worldwide, so does the demand for fuels. The transport of fuels from the point of production to the end user poses a risk of environmental pollution, both during transport and during combustion in internal combustion engines. The soil is a part of the environment which is particularly sensitive to contamination by petroleum substances. For this reason, research has been carried out into the possibility of reducing the impact of petrol on the content of heavy metals in the soil using various materials, both mineral (bentonite, calcium oxide) and organic (compost). These played an important role in the in situ remediation of contaminated soils. Petrol contamination increased the content of some heavy metals (Pb, Cd, or Ni), while it decreased the content of other metals (Cr, Zn, Co, and Cu) in the soil. The materials used in this study significantly altered the levels of heavy metals in the soil. The strength of the effect varied and the direction of the effect depended on the element. Bentonite was the most effective, while calcium oxide and especially compost were less effective. The most beneficial (limiting) effect of calcium oxide was shown on the soil content of cadmium, cobalt, and chromium, while the bentonite effects were on the content of chromium. The application of the abovementioned materials seems to be effective in reducing low level soil contamination by petrol. [ABSTRACT FROM AUTHOR]

This study explores the utilisation challenges of fly ash from municipal waste incineration, specifically focusing on ash from a dry desulphurisation plant (DDS), which is categorised as hazardous due to its high heavy metal content. The ash's low silicon and calcium contents restrict its standalone utility. Laboratory investigations initially revealed that geopolymers derived solely from fly ash after flue gas treatment (FGT), in combination with coal combustion fly ash, exhibited low compressive strength (below 0.6 MPa). However, the study demonstrated significant improvements by modifying the FGT ash through water leaching. This process enhanced its performance when mixed with high-silica and -aluminium fly ash, resulting in geopolymers achieving compressive strengths of up to 18 MPa. Comparable strength outcomes were observed when the modified ash was blended with commercial cement. Leachability tests conducted for heavy metals (HMs) such as copper, zinc, lead, cadmium, and nickel indicated that their concentrations fell below the regulatory limits for landfill disposal: 2, 4, 0.5, 0.04, and 0.4 mg/kg, respectively. These results underscore the effectiveness of water-washing FGT ash in conjunction with other materials for producing geopolymers, contributing to sustainable waste management practices. [ABSTRACT FROM AUTHOR]

The increase in the world population and the intensification of agricultural practices have resulted in the release of several contaminants into the environment, especially pesticides and heavy metals. This article reviews recent advances in using adsorbent and catalytic materials for environmental decontamination. Different materials, including clays, carbonaceous, metallic, polymeric, and hybrid materials, are evaluated for their effectiveness in pollutant removal. Adsorption is an effective technique due to its low cost, operational simplicity, and possibility of adsorbent regeneration. Catalytic processes, especially those using metallic nanoparticles, offer high efficiency in degrading complex pesticides. Combining these technologies can enhance the efficiency of remediation processes, promoting a more sustainable and practical approach to mitigate the impacts of pesticides and other agricultural pollutants on the environment. Therefore, this review article aims to present several types of materials used as adsorbents and catalysts for decontaminating ecosystems affected by agricultural pollutants. It discusses recent works in literature and future perspectives on using these materials in environmental remediation. Additionally, it explores the possibilities of using green chemistry principles in producing sustainable materials and using agro-industrial waste as precursors of new materials to remove contaminants from the environment. [ABSTRACT FROM AUTHOR]

Medium-density fiberboard (MDF) waste generation has increased steadily over the past decades, and therefore, the investigation of novel methods to recycle this waste is very important. The potential of repurposing MDF waste as an adsorbent for the treatment of Cd(II), Cu(II), Pb(II), and Zn(II) ions in water was investigated using MDF offcuts. The highest adsorption potential in single-metal ion solution systems was observed for Pb(II) ions. The experimental data of Pb(II) ions fit well with the Freundlich isotherm and pseudo-second-order kinetic models. Complexation and electrostatic interactions were identified as the adsorption mechanisms. The adsorption behavior of multi-metal ion adsorption systems was investigated by introducing Cd(II) ions as a competitive metal ion. The presence of the Cd(II) ions reduced the adsorption potential of Pb(II) ions, yet the preference for the Pb(II) ions remained. Regeneration studies were performed by using 0.1 M HCl as a regeneration agent for both systems. Even though a significant amount of adsorbed metal ions were recovered, the adsorption potential of the MDF was reduced in the subsequent adsorption cycles. Based on these results, MDF fines have the potential to be used as an economical adsorbent for remediation of wastewater containing heavy metal ions. [ABSTRACT FROM AUTHOR]

Precipitation is an important factor that influences the quality of surface water in many regions of the world. The pollution of stormwater runoff from roads and parking lots is an understudied area in water quality research. Therefore, a comprehensive analysis of the physicochemical properties of rainwater flowing from parking lots was carried out, considering heavy metals and organic micropollutants. High concentrations of zinc were observed in rainwater, in addition to alkanes, e.g., tetradecane, hexadecane, octadecane, 2,6,10-trimethyldodecane, 2-methyldodecane; phenolic derivatives, such as 2,6-dimethoxyphenol and 2,4-di-tertbutylphenol; and compounds such as benzothiazole. To remove the contaminants present in rainwater, adsorption using silica carriers of the MCF (Mesostructured Cellular Foams) type was performed. Three groups of modified carriers were prepared, i.e., (1) SH (thiol), (2) NH2 (amino), and (3) NH2/SH (amine and thiol functional groups). The research problem, which is addressed in the presented article, is concerned with the silica carrier influence of the functional group on the adsorption efficiency of micropollutants. The study included an evaluation of the effects of adsorption dose and time on the efficiency of the contaminant removal process, as well as an analysis of adsorption isotherms and reaction kinetics. The colour adsorption from rainwater was 94–95% for MCF-NH2 and MCF-NH2/SH. Zinc adsorbance was at a level of 90% for MCF-NH2, and for MCF-NH2/SH, 52%. Studies have shown the high efficacy (100%) of MCF-NH2 in removing organic micropollutants, especially phenolic compounds and benzothiazole. On the other hand, octadecane was the least susceptible to adsorption in each case. It was found that the highest efficiency of removal of organic micropollutants and zinc ions was obtained through the use of functionalized silica NH2. [ABSTRACT FROM AUTHOR]

Recent literature has exhibited a growing interest in the utilization of ground glass powder (GP) as a supplementary cementitious material (SCM). Yet, the application of SCMs in stabilizing heavy metallic and metalloid elements remains underexplored. This research zeroes in on zinc stabilization using a binder amalgam of GP and ordinary Portland cement (OPC). This study juxtaposes the stability of zinc in a recomposed binder consisting of 30% GP and 70% OPC (denoted as 30GP-M) against a reference binder of 100% CEM I 52.5 N (labeled reference mortar, RM) across curing intervals of 1, 28, and 90 days. Remarkably, the findings indicate a heightened kinetic immobilization of Zn at 90 days in the presence of GP—surging up to 40% in contrast to RM. Advanced microstructural analyses delineate the stabilization locales for Zn, including on the periphery of hydrated C3S particles (Zn–C3S), within GP-reactive sites (Si*–O–Zn), and amid C–S–H gel structures, i.e., (C/Zn)–S–H. A matrix with 30% GP bolsters the hydration process of C3S vis-à-vis the RM matrix. Probing deeper, the microstructural characterization underscores GP's prowess in Zn immobilization, particularly at the interaction zone with the paste. In the Zn milieu, it was discerning a transmutation—some products born from the GP–Portlandite reaction morph into GP–calcium–zincate. [ABSTRACT FROM AUTHOR]

Graphene oxide (GO) is considered as a promising adsorbent material for the removal of metal from aqueous environments. Here, we have used the density functional theory (DFT) approach and a combination of parameters to characterise the interactions of GO with lead (Pb) and cadmium (Cd), i.e., typical harmful metals often found in water. Our model systems consist of a singly and doubly adsorbed neutral ( Pb 0 , Cd 0 ) and charged ( Pb 2 + , Cd 2 + ) atoms adsorbed on the GO nanoparticle of the chemical formula C 30 H 14 O 15 . We show that a single charged metal ion binds more strongly than a neutral atom of the same type. Moreover, to determine the possibility of multiple adsorptions of the GO nanoparticle, two metal atoms of the same species were co-adsorbed on its surface. We found a site-dependent adsorption energy such that when two atoms of the same specie are adsorbed at sites S i and S j , the binding energy per atom depends on whether one of the two atoms is adsorbed firstly on the S i or S j sites. Furthermore, the binding energy per atom for the two co-adsorbed atoms of the same specie (i.e., neutral or charged) is less than the binding energy of a singly adsorbed atom. This suggests that atoms may become less likely to be adsorbed on the GO nanoparticle when their concentration increases. We adduce the origin of this observation to be interplay between the metal–metal interaction on the one hand and GO–metal on the other, with the former resulting in less binding for the charged adsorbed metals in particular, due to repulsive interaction between two positively charged ions. The frontier molecular orbitals analysis and the calculated global reactivity descriptors of the respective GO–metal complexes revealed that all the GO–metal complexes have a smaller HOMO–LUMO gap (HLG) relative to that of pristine metal-free GO nanoparticle. This may indicate that although the GO–metal complexes are stable, they are less stable compared to metal-free GO nanoparticles. The negative values of the chemical potentials obtained for all the GO–metal complexes further confirm their stability. Our work differs from previous experimental studies in that those lacked details of the interaction mechanisms between GO, Pb and Cd, as well as previous theoretical studies which used limited numbers of parameters to characterise the GO–metal interactions. Rather, we present a set of parameters or descriptors which provide comprehensive physical and electronic characterisation of GO–metal systems as obtained via the DFT calculations. These parameters, along with those reported in previous studies, may find applications in rational design and high-throughput screening of graphene-based materials for water purification, as an example. [ABSTRACT FROM AUTHOR]

Compound contamination of soil with heavy metals copper (Cu) and lead (Pb) triggered by mining development has become a serious problem. To solve this problem, in this paper, corncob kernel, which is widely available and inexpensive, was used as the raw material of biochar and modified by loading CaAl-layered double hydroxides to synthesize biochar-loaded CaAl-layered double hydroxide composites (CaAl-LDH/BC). After soil remediation experiments, either BC or CaAl-LDH/BC can increase soil pH, and the available phosphorus content and available potassium content in soil. Compared with BC, CaAl-LDH/BC significantly reduced the available content of Cu and Pb in the active state (diethylenetriaminepentaacetic acid extractable state) in the soil, and the passivation rate of Cu and Pb by a 2% dosage of CaAl-LDH/BC reached 47.85% and 37.9%, respectively. CaAl-LDH/BC can significantly enhance the relative abundance of beneficial microorganisms such as Actinobacteriota, Gemmatimonadota, and Luteimonas in the soil, which can help to enhance the tolerance and reduce the enrichment ability of plants to heavy metals. In addition, it was demonstrated by pea seedling (Pisum sativum L.) growing experiments that CaAl-LDH/BC increased plant fresh weight, root length, plant height, catalase (CAT) activity, and protein content, which promoted the growth of the plant. Compared with BC, CaAl-LDH/BC significantly reduced the Cu and Pb contents in pea seedlings, in which the Cu and Pb contents in pea seedlings were reduced from 31.97 mg/kg and 74.40 mg/kg to 2.92 mg/kg and 6.67 mg/kg, respectively, after a 2% dosage of CaAl-LDH/BC, which was a reduction of 90.84% and 91.03%, respectively. In conclusion, compared with BC, CaAl-LDH/BC improved soil fertility and thus the plant growth environment, and also more effectively reduced the mobility of heavy metals Cu and Pb in the soil to reduce the enrichment of Cu and Pb by plants. [ABSTRACT FROM AUTHOR]

Driven by concerns over polluted industrial wastewater, particularly heavy metals and dyes, this study explores biosorption using chemically cross-link chitosan derivatives as a sustainable and cost-effective depollution method. Chitosan cross-linking employs either water-soluble polymers and agents like glutaraldehyde or copolymerization of hydrophilic monomers with a cross-linker. Chemical cross-linking of polymers has emerged as a promising approach to enhance the wet-strength properties of materials. The chitosan thus extracted, as powder or gel, was used to adsorb heavy metals (lead (Pb2+) and copper (Cu2+)) and dyes (methylene blue (MB) and crystal violet (CV)). Extensive analysis of the physicochemical properties of both the powder and hydrogel adsorbents was conducted using a range of analytical techniques, including Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), and scanning electron microscopy (SEM), as well as 1H and 13C nuclear magnetic resonance (NMR). To gain a comprehensive understanding of the sorption process, the effect of contact time, pH, concentration, and temperature was investigated. The adsorption capacity of chitosan powder for Cu(II), Pb(II), methylene blue (MB), and crystal violet (CV) was subsequently determined as follows: 99, 75, 98, and 80%, respectively. In addition, the adsorption capacity of chitosan hydrogel for Cu(II), Pb(II), MB, and CV was as follows: 85, 95, 85, and 98%, respectively. The experimental data obtained were analyzed using the Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models. The isotherm study revealed that the adsorption equilibrium is well fitted to the Freundlich isotherm (R2 = 0.998), and the sorption capacity of both chitosan powder and hydrogel was found to be exceptionally high (approximately 98%) with the adsorbent favoring multilayer adsorption. Besides, Dubinin has given an indication that the sorption process was dominated by Van der Waals physical forces at all studied temperatures. [ABSTRACT FROM AUTHOR]

Biochar enriched with metals has an increased potential for sorption of organic and inorganic pollutants. The aim of the research was to identify the possibility of using biochar composites produced on the basis of waste plant biomass and waste FFH (ferryferrohydrosol) containing iron atoms, after CO2 capture. The composites were produced in a one-stage or two-stage pyrolysis process. Their selected properties were determined as follows: pH, ash content, C, H, N, O, specific surface area, microstructure and the presence of surface functional groups. The produced biochar and composites had different properties resulting from the production method and the additive used. The results of experiments on the removal of methylene blue (MB) from solutions allowed us to rank the adsorbents used according to the maximum dye removal value achieved as follows: BC1 (94.99%), B (84.61%), BC2 (84.09%), BC3 (83.23%) and BC4 (83.23%). In terms of maximum amoxicillin removal efficiency, the ranking is as follows: BC1 (55.49%), BC3 (23.51%), BC2 (18.13%), B (13.50%) and BC4 (5.98%). The maximum efficiency of diclofenac removal was demonstrated by adsorbents BC1 (98.71), BC3 (87.08%), BC4 (74.20%), B (36.70%) and BC2 (30.40%). The most effective removal of metals Zn, Pb and Cd from the solution was demonstrated by BC1 and BC3 composites. The final concentration of the tested metals after sorption using these composites was less than 1% of the initial concentration. The highest increase in biomass on prepared substrates was recorded for the BC5 composite. It was higher by 90% and 54% (for doses of 30 g and 15 g, respectively) in relation to the biomass growth in the soil without additives. The BC1 composite can be used in pollutant sorption processes. However, BC5 has great potential as a soil additive in crop yield and plant growth. [ABSTRACT FROM AUTHOR]

Nowadays, we have observed the dynamic development of bio-heating plants that use wood biomass for heating or energy purposes. The result of this process is a reduction in carbon dioxide emissions as well as in the production of biomass ash (BA). Despite the waste nature of BA, it should be carefully analyzed and assessed for various applications, including environmental ones. Due to the features attributed to BA, including its alkaline reaction, the high capacity of its sorption complex, relatively low salinity, and significant content of macro- and microelements, a hypothesis was put forward in this work undertaken about the positive role of BA as an immobilizing factor for Cd-, Pb-, and Zn-contaminated soils. This research was based on a pot experiment in which four series were considered: (1) BA; (2) BA + Cd; (3) BA + Pb; and (4) BA + Zn. BA was used at doses of 30, 60, and 90 mg pot−1, and metals at doses of 2 mg Cd, 100 mg Pb, and 300 mg Zn kg−1 of soil. The test plant was corn grown for green mass. The study took into account the influence of BA on the content of the total forms of heavy metals (Metot) and their available forms (Meav). In the soil without the addition of metals, a significant increase in the content of Cdtot and Cdav, and a decrease in the content of Zntot were observed due to the application of BA. The addition of metals against the background of the BA used resulted in a significant increase in Cdtot, Pbtot, and Zntot, as well as an increase in the available forms of Pbav but a decrease in Znav. However, there was no significant increase in the Cdav content. The obtained results may indicate the potentially immobilizing role of BA only in the case of zinc. They may constitute the basis for further, more detailed research aimed at determining the role of BA in the immobilization of various metals in soil. [ABSTRACT FROM AUTHOR]

Graphene oxide and its magnetic nanoparticle-based composites are a well-known tool to remove heavy metals from wastewater. Unfortunately, one of the major issues in handling such small particles consists of their difficult removal from treated wastewater (even when their magnetic properties are exploited), due to their very small diameter. One possible way to overcome this problem is to embed them in a macroscopic biopolymer matrix, such as alginate or chitosan beads. In this way, the adsorbent becomes easier to handle and can be used to build, for example, a packed column, as in a traditional industrial adsorber. In this work, the removal performances of two different embedded magnetic nanocomposite adsorbents (MNAs) are discussed. The first type of MNA is based on ferrite magnetic nanoparticles (MNPs) generated by coprecipitation using iron(II/III) salts and ammonium hydroxide, while the second is based on a 2D material composed of MNP-decorated graphene oxide. Both MNAs were embedded in cross-linked alginate beads and used to treat artificial water contaminated with chromium(III), nickel(II), and copper(II) in different concentrations. The yield of removal and differences between MNAs and non-embedded magnetic nanomaterials are also discussed. From the results, it was found that the time to reach the adsorption equilibrium is higher when compared to that of the nanomaterials only, due to the lower surface/volume ratio of the beads, but the adsorption capacity is higher, due to the additional interaction with alginate. [ABSTRACT FROM AUTHOR]

This document discusses the importance of removing heavy metals from water sources due to their increased concentrations from industrial activities. The focus is on adsorption as an effective method for removing pollutants from contaminated streams using various adsorbents. The document highlights several research papers that explore different materials and technologies for heavy metal removal, including the use of yeast cells, magnetic biocomposites, cherry pit biochar, alkali-modified sawdust, nano-biocomposites, calcined mussel shells, mineral-organic hybrid adsorbents, and natural bentonites. These studies demonstrate the potential of these materials for efficient and cost-effective heavy metal removal from water sources. [Extracted from the article]

Acid mine drainage (AMD) is a major environmental problem caused by the release of acidic, toxic, and sulfate-rich water from mining sites. This study aimed to develop novel adsorbents for the removal of chromium (Cr(VI)), cadmium (Cd(II)), and lead (Pb(II)) from simulated and actual AMD using hybrid ion-exchange resins embedded with hydrous ferric oxide (HFO). Two types of resins were synthesized: anionic exchange resin (HAIX-HFO) for Cr(VI) removal and cationic exchange resin (HCIX-HFO) for Cd(II) and Pb(II) removal. The resins were characterized using scanning electron microscopy and Raman spectroscopy, which confirmed the presence of HFO particles. Batch adsorption experiments were conducted under acidic and sulfate-enhanced conditions to evaluate the adsorption capacity and kinetics of the resins. It was found that both resins exhibited high adsorption efficiencies and fast adsorption rates for their respective metal ions. To explore the potential adsorption on actual AMD, HCIX-HFO demonstrated significant removal of some metal ions. The saturated HCIX-HFO resin was regenerated using NaCl, and a high amount of the adsorbed Cd(II) and Pb(II) was recovered. This study demonstrates that HFO-embedded hybrid ion-exchange resins are promising adsorbents for treating AMD contaminated with heavy metals. [ABSTRACT FROM AUTHOR]

This article explores recent advancements and innovative strategies in biosorption technology, with a particular focus on the removal of heavy metals, such as Cu(II), Pb(II), Cr(III), Cr(VI), Zn(II), and Ni(II), and a metalloid, As(V), from various sources. Detailed information on biosorbents, including their composition, structure, and performance metrics in heavy metal sorption, is presented. Specific attention is given to the numerical values of the adsorption capacities for each metal, showcasing the efficacy of biosorbents in removing Cu (up to 96.4%), Pb (up to 95%), Cr (up to 99.9%), Zn (up to 99%), Ni (up to 93.8%), and As (up to 92.9%) from wastewater and industrial effluents. In addition, the issue of biosorbent deactivation and failure over time is highlighted as it is crucial for the successful implementation of adsorption in practical applications. Such phenomena as blockage by other cations or chemical decomposition are reported, and chemical, thermal, and microwave treatments are indicated as effective regeneration techniques. Ongoing research should focus on the development of more resilient biosorbent materials, optimizing regeneration techniques, and exploring innovative approaches to improve the long-term performance and sustainability of biosorption technologies. The analysis showed that biosorption emerges as a promising strategy for alleviating pollutants in wastewater and industrial effluents, offering a sustainable and environmentally friendly approach to addressing water pollution challenges. [ABSTRACT FROM AUTHOR]

The studies aimed to test the adsorption capacity of two silica-enriched porous materials, synthetic Na-X zeolite and Mn-containing carbon composite, towards Pb(II) and Zn(II) ions in single and mixed systems and in the presence of diclofenac (DCF) and (or) poly(acrylic acid) (PAA). The synthetic zeolite was characterized by a well-developed surface area of 728 m2/g and a pore diameter of 1.73 nm, while the carbon composite exhibited 268 m2/g and 7.37 nm, respectively. Na-X was found to be more efficient than the carbon composite (75–212 mg/g) in adsorbing heavy metal ions in both single and bimetallic systems (322–333 mg/g). In turn, the C/Mn/SiO2 composite was more effective in removing Pb(II) ions from the systems that simultaneously contained DCF or PAA (480 and 476 mg/g, respectively). The Na-X zeolite demonstrated the greatest stability in all the systems studied. The highest stability was observed in the DCF + Pb(II) mixture, in contrast to the carbon composites where the stability was much lower. To evaluate the possibility of regeneration of the solids, HCl proved to be the best desorbent for heavy metal ions (efficiency of 99%). In general, both adsorbents offer promising potential for solving environmental problems. [ABSTRACT FROM AUTHOR]

The purpose of this manuscript is to present a review of laboratory experiments (including methodology and results) that use biochar, a specific carbon obtained by a pyrolysis process from different feedstocks, as an alternative material for heavy metal adsorption from groundwater. In recent years, many studies have been conducted regarding the application of innovative materials to water decontamination to develop a more sustainable approach to remediation processes. The use of biochar for groundwater remediation has particularly attracted the interest of researchers because it permits the reuse of materials that would be otherwise disposed of, in accordance with circular economy, and reduces the generation of greenhouse gases if compared to the use of virgin materials. A review of the different approaches and results reported in the current literature could be useful because when applying remediation technologies at the field scale, a preliminary phase in which the suitability of the adsorbent is evaluated at the lab scale is often necessary. This paper is therefore organised with a short description of the involved metals and of the biochar production and composition. A comprehensive analysis of the current knowledge related to the use of biochar in groundwater remediation at the laboratory scale to obtain the characteristic parameters of the process that are necessary for the upscaling of the technology at the field scale is also presented. An overview of the results achieved using different experimental conditions, such as the chemical properties and dosage of biochar as well as heavy metal concentrations with their different values of pH, is reported. At the end, numerical studies useful for the interpretation of the experiment results are introduced. [ABSTRACT FROM AUTHOR]

Elevated concentrations of heavy metals in natural waters can cause significant ecological problems. It is therefore essential to ensure their removal from any water discharged into the environment immediately, especially in case of an accident, where there is a risk of releasing large quantities or high concentrations. The aim of this paper is to test a newly developed adsorbent for the removal of heavy metals from aqueous solutions—in particular, it is very fast adsorption, and thus efficiency, during clean-ups. The alkali-activated foamed zeolite adsorbent was laboratory-prepared and -tested in both batch and flow-through arrangements on single and multi-component solutions and compared with natural zeolite. The experimental setup for batch adsorption consisted of a set of samples and solutions containing iron, cobalt, manganese, zinc and nickel. The samples were put on a horizontal shaker with a 500 mg adsorbent loading in a 50 mL solution. The column adsorption experimental setup consisted of a glass column with an inside diameter of 15 mm and a bed length of 165 mm. A measured amount of each adsorbent was added to the column to achieve a filter fixed-bed height of 160 mm. The high efficiency of the tested adsorbent on various heavy metals was confirmed. The adsorbent has a high potential for use in decontamination processes, water protection and landscape revitalization. Due to its rapid precipitation and subsequent fixation of metal cations in the form of insoluble oxide or hydroxide, it can be used as an emergency adsorbent, the great advantage of which is its low production cost and natural origin. [ABSTRACT FROM AUTHOR]

Valorization of high-volume mine tailings could be achieved by the development of new geopolymers with a low CO2 footprint. Materials rich in aluminum and silicon with appropriate solubility in an alkaline medium can be used to obtain a geopolymer. This paper presents a study of copper mine tailings from Bulgaria as precursors for geopolymers. Particle size distribution, chemical and mineralogical composition, as well as alkaline reactivity, acidity and electroconductivity of aqueous slurry are studied. The heavy metal content and their mobility are studied by leaching tests. Sequential extraction was applied to determine the geochemical phase distribution of heavy metals. The studied samples were characterized by high alkalinity, which could favor the geopolymerization process. The water-soluble sulphates were less than 4%. The Si/Al ratio in mine tailing was found to be 3. The alkaline reactivity depended more so on the time of extraction than on the concentration of NaOH solution. The main part of the heavy metals was found in the residual fraction; hence, in high alkaline medium during the geopolymerization process, they will stay fixed. Thus, the obtained geopolymers could be expected to exert low environmental impact. The presented results revealed that studied copper mine tailing is a suitable precursor for geopolymerization. [ABSTRACT FROM AUTHOR]

This study aimed to investigate the efficiency of a geopolymer binder of the type of Na-poly(ferro–silico–aluminate) as a matrix for the stabilization of heavy metals along with their effect on the development of structural performances. The artificial contamination of soil with ions was carried out and used to prepare an alkali-activated iron-rich lateritic soil binder. Further, various microstructural analyses were carried out to explain the stabilization mechanism. The stabilization efficiency was assessed by leaching tests in de-ionized water and hydrochloric acid (0.1 M, HCl). Then, the physical properties were determined to evaluate the impact of heavy metals on the structural performance of the binder. Results demonstrated that the prepared geopolymer binder has the lowest stabilization capacity in an acidic medium (low pH) than in water with high pH. However, the stabilization of Cu ions was effective at 99%, while the Cd ion is barely retained in the matrix. Firstly, the mechanism consists of chemical bonds through ion exchange with sodium of the Na-poly(ferro–silico–aluminate) network. Secondly, through physical interaction with the pore network of the matrix, the heavy metals induced structural deterioration in the geopolymer matrix with a decrease in the compressive strength and bulk density and an increase of both apparent porosity and water absorption. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Soil contamination through heavy metals (HMs) is a serious environmental problem that needs to be addressed. One of the methods of remediating soils contaminated with HMs and reducing the environmental risks associated with them is to immobilize these HMs in the soil using specific amendment(s). The use of biochar as an organic amendment can be an environmentally friendly and practically feasible option, as (i) different types of biomass can be used for biochar production, which contributes to environmental sustainability, and (ii) the functionality of biochar can be improved, enabling efficient immobilization of HMs. Effective use of biochar to immobilize HMs in soil often requires modification of pristine biochar. There are various physical, chemical, and biological methods for modifying biochar that can be used at different stages of pyrolysis, i.e., before pyrolysis, during pyrolysis, and after pyrolysis. Such methods are still being intensively developed by testing different modification approaches in single or hybrid systems and investigating their effects on the immobilization of HMs in the soil and on the properties of the remediated soil. In general, there is more information on biochar modification and its performance in HM immobilization with physical and chemical methods than with microbial methods. This review provides an overview of the main biochar modification strategies related to the pyrolysis process. In addition, recent advances in biochar modification using physical and chemical methods, biochar-based composites, and biochar modified with HM-tolerant microorganisms are presented, including the effects of these methods on biochar properties and the immobilization of HMs in soil. Since modified biochar can have some negative effects, these issues are also addressed. Finally, future directions for modified biochar research are suggested in terms of scope, scale, timeframe, and risk assessment. This review aims to popularize the in situ immobilization of HMs with modified biochar. [ABSTRACT FROM AUTHOR]

Environmental pollution has been widely considered by researchers, especially the heavy metals damage to the human and ecological environment is irreversible. Adsorption is an important method to remove heavy metal ions from the environment. In this paper, humic acid (HA) was functionalized by the improved Hummers method, and its adsorption capacity for Pb(II) was studied. The results of scanning electron microscope (SEM), X-ray diffraction (XRD), Roman, and Brunauer-Emmett-Teller (BET) showed that the thickness of irregular particles decreases to a layered structure during the transformation process. In addition, X-ray photoelectron spectroscopic (XPS) and Fourier transform infrared spectra (FT-IR) spectra showed that the surface of oxidized-biochar (OBC) was rich in reactive oxygen species, which was conducive to the formation of coordination bonds with Pb(II). Further adsorption experiments showed that it was a spontaneous monolayer chemisorption. The results of the DFT calculation showed that -COOH had the lowest adsorption energy for Pb(II), and it was easier to form stable chemical bonds than -OH, -C=O, and -C-O-C-. Because those oxygen-containing functional groups not only can promote electrostatic attraction but also are more favorable for forming a covalent bond with Pb(II). This study had guiding significance for the deep modification and application of weathered coal as a heavy metal ion adsorbent or cation exchanger. [ABSTRACT FROM AUTHOR]

Detecting heavy metals in seawater is challenging due to the high salinity and complex composition, which cause strong interference. To address this issue, we propose using a multistage energy barrier as an electrochemical driver to generate electrochemical responses that can resist interference. The Ni-based heterojunction foams with different types of barriers were fabricated to detect Cr(VI), and the effects of the energy barriers on the electrochemical response were studied. The single-stage barrier can effectively drive the electrochemical response, and the multistage barrier is even more powerful in improving sensing performance. A prototype Ni/NiO/CeO2/Au/PANI foam with multistage barriers achieved a high sensitivity and recovery rate (93.63–104.79%) in detecting seawater while resisting interference. The use of multistage barriers as a driver to resist electrochemical interference is a promising approach. [ABSTRACT FROM AUTHOR]

The increasing accumulation of rock waste obtained due to ore processing and its environmental impacts, such as acid mine drainage and elevated concentrations of heavy metals in soils, necessitates the transformation of mining technologies based on the concept of circular waste management. The research is aimed at improving the parameters of the mechanical activation effect produced on technogenic georesources, as well as at expanding the application scope of disintegrators in the field of using the partial backfill of the mined-out space when developing stratified deposits. In this regard, the research purpose was to substantiate the parameters of extracting metals from enrichment tailings using their mechanochemical activation to ensure cyclic waste management. The research involved the application of three-dimensional interpolation methods used for processing the data and the graphical representation. As a result, the following was found to be characteristic of the waste of the Sadonsky mine management. The degree of extracting zinc from pre-activated tailings increases logarithmically when the H2SO4 concentration and the NaCl proportion decrease 3.5 times. The degree of extracting lead from the activated tailings increases according to the Fourier law when decreasing the NaCl mass concentration, and an optimal range of the H2SO4 (0.38–0.51%) proportion decreases six times. One of the key results of the research is the justification of expanding the scope of applying disintegrators in the case of a directed activation influence exerted on the components of the stowing strips. The obtained results expand the understanding of the mechanism of the influence of the mechanochemical activation of dry tailings on the reactivity unevenness when extracting several metals from them. [ABSTRACT FROM AUTHOR]

Soil pollution with heavy metals is a problem for the whole geosystem. The aim of the research is to identify new solutions for extracting heavy metals from polluted soils so that they can be further exploited. To this end, investigations of the physicochemical characteristics of the soil sample under study were carried out. Following the analyses, the soil was characterised as lute-coarse sand (UG) with a strongly acidic pH (4.67), a hygroscopicity coefficient (CH = 4.8% g/g), and a good supply of nutrients: nitrogen (Nt): 0.107%; mobile phosphorus (PAL): 6 mg kg−1 and mobile potassium (KAL): 26 mg kg−1, but is low in humus (2.12%). The metal content of the soil was determined by atomic absorption spectrometry (AAS), and the analyses showed high concentrations of metals (Pb: 27,660 mg kg−1; Cu: 5590 mg kg−1; Zn: 2199 mg kg−1; Cd: 11.68 mg kg−1; Cr: 146 mg kg−1). The removal of metals (Pb, Cu, Zn, Cd, and Cr) from polluted soil by different extraction agents (water, humus, malic acid, chitosan, and gluconic acid) was investigated. Metal extraction experiments were carried out in a continuous orbital rotation-oscillation stirrer at a solid/liquid/ (S/L ratio; g:mL) of 1:4, at two concentrations of extraction solution (1% and 3%), and at different stirring times (2, 4, 6, and 8 h). The yield of the extraction process is very low for all proposed extraction solutions. The maximum values of extraction efficiency are: 0.5% (Pb); 3.28% (Zn); and 5.72% (Cu). Higher values were obtained in the case of Cr (11.97%) in the variant of using humus 3% as an extraction solution at a stirring time of 6 h. In the investigated experimental conditions, the best removal efficiencies were obtained in the case of cadmium (26.71%) when using a 3% malic acid solution. In conclusion, it is considered that, from case to case, the type of extraction solution as well as the nature of the metal influence the mechanism of the depollution process, i.e., the capacity of the fine soil granules to free themselves from the pollutant metal that has adhered to them, and further research is considered necessary in the future. [ABSTRACT FROM AUTHOR]

Medical waste incineration fly ash (MWIFA) contains heavy metals that are toxic by nature and pose numerous health risks. The paper deals with the suitability of MWIFA as a mineral filler in the bituminous layer as an alternative to conventional stone dust (SD) through an appropriate combination of engineering and environmental assessments. Engineering parameters, such as Marshall stability, stability loss, flow, unit weight, air voids (Va), voids filled with asphalt (VFA), and voids in the mineral aggregate (VMA) of the asphalt mixtures, were evaluated with varying filler ratios, from 2% to 10%. All parameters for both fillers at optimum bitumen content satisfied the Marshall Mix Design criteria. The optimum bitumen contents of all filler ratios were within the standard limit recommended by the Bangladesh Roads and Highways Department. It was found that mixes prepared with MWIFA can resist moisture effects, making them durable in the monsoon. The mixes with 5.5% MWIFA as mineral filler performed the best, whereas 9% SD filler was required to achieve similar performance. The environmental test results show no environmental restriction on stabilizing the MWIFA into paving mixtures. The mobility of heavy metals (As, Pb, Cu, Cr, Ni, Cd, Hg, and Zn) from the asphalt-MWIFA mix was insignificant. The cumulative concentrations of heavy metals (Cd, Ni, Zn, Cu, and Pb) from long-term leaching tests were far below the Dutch regulatory limit (U1). MWIFA can be considered an eco-friendly and sustainable mineral filler for the dense bituminous pavement layer. [ABSTRACT FROM AUTHOR]

Bentonitic clay and wood sawdust are natural materials widely available in nature at low cost with high heavy metals sorption properties that, in this work, were combined to achieve an effective composite biosorbent with high sorption properties and enhanced mechanical stability. Pine, aspen, and birch wood sawdust, as well as different bentonite clays and different sawdust modification methods (H3PO4 or HCl) were used for preparing new composite biosorbents. A mixture of wood sawdust and bentonite in a ratio of 2:1 was used. All materials were characterized by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscope (SEM) methods and tested for Cu and Ni ions removal from water. The adsorption process for all composite biosorbents was well described from a pseudo-second order kinetic model (R2 > 0.9999) with a very high initial adsorption rate of Cu and Ni ions and a maximum uptake recorded within 2 h. The results have shown that the adsorption capacity depends mainly on the kind of wood and the acid treatment of the wood that enhances the adsorption capacity. At a concentration of 50 mg/L, the biosorbent prepared using birch wood sawdust showed the worst performance, removing barely 30% of Cu and Ni ions, while aspen wood sawdust improved the adsorption of Cu (88.6%) and Ni (52.4%) ions. Finally, composite biosorbent with pine wood sawdust showed the best adsorption be haviour with an efficiency removal of 98.2 and 96.3% of Cu and Ni ions, respectively, making it a good candidate as an inexpensive and effective biosorbent for the removal of heavy metals. [ABSTRACT FROM AUTHOR]

Palygorskite is an aluminum and magnesium silicate characterized by its fibrous morphology, providing it with great versatility in industrial applications, including pharmaceuticals. Although most of the reserves are in the United States, in recent years occurrences of commercially exploited deposits in Brazil have been recorded, mainly in the country's northeast region. This has motivated this study, which analyzes raw Brazilian palygorskite compared to a commercial sample (Pharmasorb® colloidal) to demonstrate its pharmaceutical potential. The chemical and mineral composition of the samples were evaluated for surface properties, granulometry, morphology, crystallography, thermal analysis, and spectroscopy. Raw palygorskite presented 67% purity, against 74% for Pharmasorb® colloidal. The percentage purity relates to the presence of contaminants, mainly carbonates and quartz (harmless under conventional conditions of pharmaceutical use). Furthermore, it was possible to confirm the chemical composition of these phyllosilicates, formed primarily of silicon, aluminum, and magnesium oxides. The crystallographic and spectroscopic profiles were consistent in both samples, showing characteristic peaks for palygorskite (2θ = 8.3°) and bands attributed to fibrous phyllosilicates below 1200 cm−1, respectively. The thermal analysis allowed the identification of the main events of palygorskite, with slight differences between the evaluated samples: loss of water adsorbed onto the surface (~85 °C), removal of water contained in the channels (~200 °C), coordinated water loss (~475 °C), and, finally, the dehydroxylation (>620 °C). The physicochemical characteristics of raw palygorskite align with pharmacopeial specifications, exhibiting a high specific surface area (122 m2/g), moderately negative charge (−13.1 mV), and compliance with the required limits for heavy metals and arsenic. These favorable technical attributes indicate promising prospects for its use as a pharmaceutical ingredient in the production of medicines and cosmetics. [ABSTRACT FROM AUTHOR]

In this study, inert dry bioadsorbents prepared from corn cob residues (CCR), cocoa husk (CH), plantain peels (PP), and cassava peels (CP) were used as adsorbents of heavy metal ions (Pb2+ and Ni2+) in single-batch adsorption experiments from synthetic aqueous solutions. The physicochemical properties of the bioadsorbents and the adsorption mechanisms were evaluated using different experimental techniques. The results showed that electrostatic attraction, cation exchange, and surface complexation were the main mechanisms involved in the adsorption of metals onto the evaluated bioadsorbents. The percentage removal of Pb2+ and Ni2+ increased with higher adsorbent dosage, with Pb2+ exhibiting greater biosorption capacity than Ni2+. The bioadsorbents showed promising potential for adsorbing Pb2+ with monolayer adsorption capacities of 699.267, 568.794, 101.535, and 116.820 mg/g when using PP, CCR, CH, and CP, respectively. For Ni2+, Langmuir's parameter had values of 10.402, 26.984, 18.883, and 21.615, respectively, for PP, CCR, CH, and CP. Kinetics data fitted by the pseudo-second-order model revealed that the adsorption rate follows this order: CH > CP > CCR > PP for Pb2+, and CH > CCR > PP > CP for Ni2+. The adsorption mechanism was found to be controlled by ion exchange and precipitation. These findings suggest that the dry raw biomasses of corn cob residues, cocoa husk, cassava, and plantain peels can effectively remove lead and nickel, but further research is needed to explore their application in industrial-scale and continuous systems. [ABSTRACT FROM AUTHOR]

The article presents studies of the influence of parameters of synthesis modes and alkali concentration on the synthesis of zeolite materials from coal fly ash (CFA). The purpose of the study was to synthesise zeolite materials from CFA using the method of alkaline fusion and to determine the susceptibility of selected heavy-metal ions to removal from solutions in an ion exchange process on a selected mesoporous zeolite. It was found that the crystalline phase of sodalite was dominated in all of the samples synthesized. The specific surface area (SBET) of the samples was evaluated using the standard Brunauer–Emmett–Teller (BET) method using N2 sorption. Crystalline zeolite materials have been used to study the efficiency of removing heavy metals from aqueous solutions of Ni2+, Cd2+ and Pb2+. The adsorption data were analyzed using the Langmuir and Freundlich isotherm model. When comparing the estimated coefficient of determination (r2), it was noticed that the sorption data are more accurately described by the Langmuir isotherm and the pseudo-second-order kinetic model. The results of metal adsorption experiments suggest that the synthesized zeolite material has great potential to be used as an inexpensive and alternative source in the production of adsorbents. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

In the present work, activated-carbon-containing pellets were preparedby direct chemical activation of sawdust, using clays as a binder. The obtained pellets (ACC) were coated with hydroxyapatite (HAp) nanoparticles (ACC-HAp) to improve adsorption towards Pb(II), Cu(II), Zn(II), and Ni(II). The pellets were characterized by scanning electron microscopy (SEM), by Fourier transform infrared spectroscopy (FTIR), and with a gas sorptometer. The effect of pH, contact time, and initial concentration on adsorption performance was investigated. Additionally, desorption studies were performed, and the regeneration influence on compressive strength and repeated Pb(II) adsorption was investigated. The results showed that, after coating ACC pellets with HAp nanoparticles, the adsorption capacity increased for all applied heavy metal ions. Pb(II) was adsorbed the most, and the best results were achieved at pH 6. The adsorption process followed the pseudo-second-order kinetic model. The adsorption isotherm of Pb(II) is better fitted to the Langmuir model, showing the maximum adsorption capacity of 56 and 47 mg/g by ACC-HAp and ACC pellets, respectively. The desorption efficiency of Pb(II)-loaded ACC-HAp pellets increased by lowering the pH of the acid, resulting in the dissolution of the HAp coating. The best desorption results were achieved with HCl at pH 1 and 1.5. Therefore, the regeneration procedure consisted of desorption, rinsing with distilled water, and re-coating with HAp nanoparticles. After the regeneration process, the Pb(II) adsorption was not affected. However, the desorption stage within the regeneration process decreased the compressive strength of the pellets. [ABSTRACT FROM AUTHOR]

By utilizing low-grade bauxite desilication solution as raw material and adding lime after thermal reaction, adsorbent MCS was synthesized. X-ray diffraction, Brunauer–Emmett–Teller, Fourier transform infrared spectroscopy, and scanning electron microscopy were used to characterize the MCS, MCS-Pb, and MCS-Cu. The Freundlich model was found to be more suitable for isothermal adsorption, suggesting that the adsorption of Cu2+ and Pb2+ by MCS is not limited to monolayer adsorption. According to the results of the experiment, the maximum adsorption capacities of lead ion and copper ion were found to be Pb2+ (1921.506 mg/g) > Cu2+ (561.885 mg/g), and the adsorption was controlled by chemical reactions following pseudo-second-order kinetics. Electrolyte study results indicated that the presence of background electrolyte did not affect the adsorption of Cu2+ and Pb2+ by MCS. [ABSTRACT FROM AUTHOR]

The developed karst caves may become the seepage channels of heavy metal to the soil and underground water in Southwest China. Therefore, it is necessary to apply effective seepage treatments to the base of heavy metal tailing reservoirs. This paper addressed the high-pressure rotary jet technology and slurry systems used in the seepage treatment of the deep tailing sand of the Shenxiandong tailing pond located in Southwest China. In this study, the factors of fluidity, initial and final setting times, compressive strength, and permeability coefficient of the slurry were conducted. The mechanism analysis was investigated by X-ray diffraction (XRD), scanning electron microscope (SEM), and inductively coupled plasma-mass spectrometry (ICP-MS). Three different types of slurry systems were proposed, and the permeability coefficients of the solidification body following 28 days of curing were less than 1 × 10−7 cm/s. The concentrations of Pb and Zn in the slurry system containing bentonite were reduced by 26.2% and 45.7%, respectively. In the presence of slaked lime and fly ash, the concentrations of Pb and Zn could be reduced by 26.8% and 30%, respectively. A total of 2142 high-pressure rotary jet piles were completed by the high-pressure rotary jet method in the field trial. The diffusion radius of these piles was over 1 m. Following 28 days of curing, the solidification body's compressive strength was 7.45 MPa and the permeability coefficient was 6.27 × 10−8 cm/s. Both the laboratory and on-site trials showed that this method produced a good pollution barrier effect, which could prevent the diffusion of heavy metal into the adjacent underground water through the karst caves. It is also an effective way of engineering technology concerning heavy metal pollution control that occurs in tailing ponds. [ABSTRACT FROM AUTHOR]

This study investigates the possibility of using municipal solid waste incineration fly ash as a supplementary cementitious material to replace part of the clinker in cement. Life cycle assessment has shown that the partial replacement of clinker with blast furnace slag (CEM III) reduces cement's global warming potential by ~30%, while replacing clinker with fly ash reduces it by up to 55%. When using CEM III as the control binder in cement in which 55 wt% of the clinker was replaced with hydrothermally treated fly ash, the flexural strength decreased by ~60% and the compressive strength by ~65%. When the fly ash was mixed with calcined and vitrified demolition materials, flexural strength decreased by ~30% and compressive strength by ~50%. The hardening of the hydraulic binders fixed the heavy metals in the municipal solid waste incineration fly ash. [ABSTRACT FROM AUTHOR]

Water pollution due to heavy metal ions has become a persistent and increasing problem globally. To combat this, carbonaceous materials have been explored as possible adsorbents of these metal ions from solution. The problem with using these materials on their own is that their lifespan and, therefore, usability is reduced. Hence the need to mask them and an interest in using polymers to do so is picked. This introduces an improvement into other properties as well and opens the way for more applications. This work gives a detailed review of the major carbonaceous materials, graphene and graphene oxide, outlining their origin as well as morphological studies. It also outlines the findings on their effectiveness in removing heavy metal ions from water, as well as their water absorption properties. The section further reports on graphene/polymer and graphene oxide/polymer composites previously studied and their morphological as well as thermal properties. Then the work done in the absorption and adsorption capabilities of these composites is explored, thereby contrasting the two materials. This enables us to choose the optimal material for the desired outcome of advancing further in the utilization of carbonaceous material-based polymer composites to remove heavy metal ions from water. [ABSTRACT FROM AUTHOR]

Water pollution caused by the leakage and discharge of pollutants, such as dyes and heavy metal ions, can cause serious damage to the environment and human health. Therefore, it is important to design and develop adsorbent materials that are efficient and multifunctional for the removal of these pollutants. In this work, poly(vinyl alcohol-co-ethylene) (EVOH)/polyaniline (PANI) composite nanofibrous aerogels (NFAs) were fabricated via solution oxidation and blending. The aerogels were characterized by a scanning electron microscope, Fourier transform infrared spectrometry, a contact angle measuring instrument and a universal testing machine. The influences of the introduction of PANI nanorods on the structural properties of aerogels were investigated, and the adsorption performance of aerogels was also studied. The results showed that the introduction of PANI nanorods filled the fibrous network structure, reduced porosity, increased surface hydrophilicity and improved compressive strength. Furthermore, EVOH/PANI composite NFAs possess good adsorption performances for dyes and heavy metal ions: The adsorption capacities of methyl orange and chromium ions (VI) are 73.22 mg/g and 115.54 mg/g, respectively. Overall, the research suggests that EVOH/PANI NFAs have great potential as efficient and multifunctional adsorbent materials for the removal of pollutants from water. [ABSTRACT FROM AUTHOR]

The aim of the work was to develop a zero-waste technological solution for hybrid removal of heavy metals from river sediments. The proposed technological process consists of sample preparation, sediment washing (a physicochemical process for sediment purification), and purification of the wastewater produced as a by-product. A suitable solvent for heavy metal washing and the effectiveness of heavy metal removal were determined by testing EDTA and citric acid. The process for removing heavy metals from the samples worked best with citric acid when the 2% sample suspension was washed over a 5-h period. The method was chosen of the adsorption of heavy metals from the exhausting washing solution on natural clay. Analyses were performed of the three main heavy metals, Cu(II), Cr(VI), and Ni(II), in the washing solution. Based on the laboratory experiments, a technological plan was prepared for the purification of 100,000 tons of material per year. [ABSTRACT FROM AUTHOR]

Cadmium (Cd), as a type of heavy metal, can increase the incidence of many diseases, even in low concentrations. In this study, tobermorite was hydrothermally synthesized and then applied to adsorb Cd2+ from an aqueous solution. The physicochemical characteristics of the synthesized tobermorite were detected, and the results indicated that the well-crystallized tobermorite had a lot of mesopores and a large specific surface area of 140.92 m2/g. It acquired a pH self-adjustment ability via spontaneously releasing Ca2+ and OH- into the aqueous solution. The effects of different factors on Cd2+ removal were investigated. For Cd2+, the removal efficiency could reach 99.71% and the maximum adsorption capacity was 39.18 mg/g using tobermorite. The adsorption data was best fitted with the pseudo-second-order kinetic and Langmuir isotherm models. In addition, there was no strict limit on the solution pH in Cd2+ adsorption because the tobermorite could adjust the solution pH to an alkaline atmosphere spontaneously. The efficient removal of Cd2+ using tobermorite was a result of surface complexation and ion exchange. [ABSTRACT FROM AUTHOR]

Rice husk was converted into activated carbon (AC) as a byproduct of agricultural waste in an electric furnace at 700 °C and chemically activated using three distinct processes: NaOH AC(C), acetic acid AC(C-1), phosphoric acid AC(C-2), and carbonization AC(C-3) without any chemical activation. To characterize the activated carbon and the removal efficiencies of Fe(III) and Mn(II) from aqueous solutions, various analytical tools were used. The results revealed that the capacities of the four adsorbents to adsorb Fe(III) or Mn(II) from an aqueous solution differ significantly. AC(C-3) was chosen for additional research. The impact of different operational factors, including pH, contact time, adsorbent dosage, starting metal ion concentration, interfering ions, and temperature, were investigated. The optimum pH values for Fe(III) and Mn(II) adsorption were found to be pH 3 and pH 6, respectively. The results obtained were utilized to assess the kinetics and thermodynamics of the adsorption process. The sorption of Fe(III) and Mn(II) ions was found to be a pseudo-second-order kinetic process, and the equilibrium data were fitted with the Langmuir isotherm. Additionally, the evidence suggests that an endothermic mechanism governs the adsorption process. The maximum adsorption capacities of Fe(III) and Mn(II) were 28.9 and 73.47 mg/g, respectively. [ABSTRACT FROM AUTHOR]

A passive treatment process using sulfate-reducing bacteria (SRB) is known to be effective in removing heavy metals from acid mine drainage (AMD), though there has been little discussion of the mechanism involved to date. In this work, a sulfate-reducing column test was carried out using supplementary ethanol as an electron donor for microorganisms, and the reaction mechanism was examined using geochemical modeling and X-ray absorption fine structure (XAFS) analysis. The results showed that Cu was readily removed from the AMD on the top surface of the column (0–0.2 m), while Zn and Cd depletion was initiated in the middle of the column (0.2–0.4 m), where sulfide formation by SRB became noticeable. Calculations by a developed geochemical model suggested that ethanol decomposition by aerobic microbes contributed to the reduction of Cu, while sulfide produced by SRB was the major cause of Zn and Cd removal. XAFS analysis of column residue detected ZnS, ZnSO4 (ZnS oxidized by atmospheric exposure during the drying process), and CuCO3, thus confirming the validity of the developed geochemical model. Based on these results, the application of the constructed geochemical model to AMD treatment with SRB could be a useful approach in predicting the behavior of heavy metal removal. [ABSTRACT FROM AUTHOR]

Phosphate rocks (PRs) play a crucial role in ensuring the availability of phosphorous for the world's food needs. PRs are used to manufacture phosphoric acid in the wet process as well as P-fertilizers. The chemical and mineralogical compositions of PRs from Djebel Onk (Algeria), Khneifiss (Syria), Negev (Israel), Bou Craa (Morocco), and Khouribga (Morocco) are discussed in this study. PRs were characterized by inductively coupled plasma optical emission spectrometry (ICP-OES), cold vapor atomic absorption spectrometry (CVAAS), ion chromatography (IC), and X-ray diffraction (XRD), as well as gravimetric and potentiometric methods. All PRs were mainly composed of CaO, P2O5, SiO2, F, SO3, Na2O, MgO, Al2O3, Fe2O3, SrO, and K2O at the level of wt.%. The P2O5 content accounted for 28.7–31.2%, which indicates that these are beneficial rocks to a marketable product. The degree of PR purity expressed by the minor elements ratio index (MER index) varied from 2.46% to 10.4%, and the CaO/P2O5 weight ratio from 1.6 to 1.9. In addition, the occurrence of trace elements such as As, Cd, Cr, Cu, Hg, Mn, Ni, Pb, Ti, V, U, and Zn, as well as Cr(VI) and Cl ions at the level of mg∙kg−1 was found. Since PRs will be used to produce P-fertilizers, their composition was compared with the regulatory parameters set up by EU Regulation 2019/1009 related to the heavy metals (As, Cd, Pb, Ni, Hg, Cu, Zn) and Cr(VI) contents in inorganic fertilizers. The heavy metals and Cr(VI) content in all PRs did not exceed the limit values. XRD analysis revealed that fluorapatite, hydroxyapatite, carbonate fluorapatite, and carbonate hydroxyapatite were the dominant minerals. The accuracy and precision of the used methods were evaluated by analysis of standard reference materials (SRM) for Western Phosphate Rock (NIST 694). The recovery was 85.3% for U and 109% for K2O, and the RSD ranged from 0.67% to 12.8%. [ABSTRACT FROM AUTHOR]

The present study described three synthesis routes using different natural polysaccharides as low-cost non-toxic fuels and complexing agents for obtaining MgO. Cassava starch, Aloe vera leaves (mainly acemannan) gel, and citric pectin powder were mixed with magnesium nitrate salt and calcined at 750 °C for 2 h. The samples were named according to the polysaccharide: cassava starch (MgO-St), citrus pectin (MgO-CP), and Aloe vera (MgO-Av). X-ray diffraction identified the formation of a monophasic periclase structure (FCC type) for the three samples. The N2 adsorption/desorption isotherms (B.E.T. method) showed an important difference in textural properties, with a higher pore volume (Vmax = 89.76 cc/g) and higher surface area (SA = 43.93 m2/g) obtained for MgO-St, followed by MgO-CP (Vmax = 11.01 cc/g; SA = 7.01 m2/g) and MgO-Av (Vmax = 6.44 cc/g; SA = 6.63 m2/g). These data were consistent with the porous appearance observed in SEM images. Porous solids are interesting as adsorbents for removing metallic and molecular ions from wastewater. The removal of copper ions from water was evaluated, and the experimental data at equilibrium were adjusted according to the Freundlich, Langmuir, and Temkin isotherms. According to the Langmuir model, the maximum adsorption capacity (qmax) was 6331.117, 5831.244, and 6726.623 mg·g−1 for the adsorbents MgO-St, MgO-Av, and MgO-CP, respectively. The results of the adsorption isotherms indicated that the synthesized magnesium oxides could be used to decrease the amount of Cu2+ ions in wastewater. [ABSTRACT FROM AUTHOR]

Exploration of sensitive and selective fluorescence sensors towards toxic metal species is of great importance to solve metal pollution issues. In this work, a three-dimensional (3D) strontium coordination polymer of Sr2(tcbpe) (H4tcbpe = 1,1,2,2-tetrakis(4-(4-carboxy-phenyl)phenyl)ethene) has been synthesized and developed as a fluorescent sensor to Fe3+ ions. Sr2(tcbpe) shows a mechanochromic fluorescence with emission shifting from blue of the pristine to green after being ground. Notably, based on a fluorescence quenching mechanism, Sr2(tcbpe) displays a sensitive and selective fluorescent sensing behavior to Fe3+ ions with a detection limit of 0.14 mM. Moreover, Sr2(tcbpe) exhibits high tolerance to water in a wide pH range (pH = 3–13), demonstrating that Sr2(tcbpe) is a potential fluorescent sensor of Fe3+ in water. [ABSTRACT FROM AUTHOR]

This work shows the development and characterization of two zeolite structures by recycling PV glass and coal fly ash for the removal of cadmium, copper, and lead from synthetic solutions containing one or three cations. The materials were characterized in terms of crystalline structure (XRD), morphology (SEM, AFM), and specific surface. For increasing the heavy-metals removal efficiency, the adsorption conditions, such as substrate dosage, preliminary concentration, and contact time, were optimized. The pseudo-second-order kinetic model adsorption kinetics fit well to describe the activity of the zeolites ZFAGPV-A and ZFAGPV-S. The zeolite adsorption equilibrium data were expressed using Langmuir and Freundlich models. The highest adsorption capacities of the ZFAGPV-A zeolite are qmaxCd = 55.56 mg/g, qmaxCu = 60.11 mg/g, qmaxPb = 175.44 mg/g, and of ZFAGPV-S, are qmaxCd = 33.45 mg/g, qmaxCu = 54.95 mg/g, qmaxPb = 158.73 mg/g, respectively. This study demonstrated a new opportunity for waste recycling for applications in removing toxic heavy metals from wastewater. [ABSTRACT FROM AUTHOR]

Oily sludge is recognized as hazardous waste. To reduce the potential danger and harmful factors of oily sludge, it is very important to analyze its environmental risk. In this paper, the characterization of oily sludge from Shengli Oilfield in China was tested experimentally, including the composition content, particle size, microscopic morphology, heavy metal content, organic composition, inorganic composition, and thermogravimetric analysis, which were used to analyze environmental risks. The results show that the oil content of oily sludge is as high as 10.3%, which will cause serious pollution. It is calculated that China can recover 772.5 million liters of oil and reduce 553.9 million kg of carbon emissions compared with incineration in one year, if the oily sludge can be managed effectively. The content of heavy metals such as Ba, Zn, Cr, As, Ni, Se, Be, and Hg in oily sludge exceeds the standard. It will restrain the self-healing ability of soil, pollute groundwater, and endanger animals and plants. The organic matter of oily sludge is concentrated in C11 to C29. It contains a large amount of benzene series and polycyclic benzene hydrocarbons, which can lead to cancer in the human body. Inorganic substances in oily sludge are mixed with some additives, which can not only reduce the toxicity of heavy metals, but also be used as building materials. The median particle size D50 of oily sludge is 0.91 μm, and it spreads all over the narrow pores. Generally, it needs to be treated under high temperature conditions, which will cause secondary pollution to the environment. The research content of this paper provides a theoretical reference for the management of oily sludge. [ABSTRACT FROM AUTHOR]

The cadmium-contaminated water body is a worldwide concern for the environment and toxic to human beings and the removal of cadmium ions from drinking and groundwater sustainably and cost-effectively is important. A novel nano-biocomposite was obtained by impregnating silver nanoparticles (AgNPs) within kenaf-based activated carbon (KAC) in the presence of chitosan matrix (CS) by a simple, facile photoirradiation method. The nano-biocomposite (CS-KAC-Ag) was characterized by an environmental scanning electron microscope equipped with energy dispersive X-ray spectroscopy (ESEM-EDX), Fourier-transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) method. A Box–Behnken design of response surface methodology (RSM) was used to optimize the adsorption of Cd2+. It was found that 95.1% of Cd2+ (10 mg L−1) was eliminated at pH 9, contact time of 120 min, and adsorbent dosage of 20 mg, respectively. The adsorption of Cd2+ by CS-KAC-Ag is also in agreement with the pseudo-second-order kinetic model with an R2 (coefficient of determination) factor greater than 99%. The lab data were also corroborated by tests conducted using water samples collected from mining sites in Mexico. Along with Cd2+, the CS-KAC-Ag exhibited superior removal efficiency towards Cr6+ (91.7%) > Ni2+ (84.4%) > Co2+ (80.5%) at pH 6.5 and 0.2 g L−1 dose of the nano-adsorbent. Moreover, the adsorbent was regenerated, and the adsorption capacity remained unaltered after five successive cycles. The results showed that synthesized CS-KAC-Ag was a biocompatible and versatile porous filtering material for the decontamination of different toxic metal ions. [ABSTRACT FROM AUTHOR]