Search Results (1,843)

Mercury contamination in water poses severe environmental and health risks, requiring efficient and sustainable removal strategies. In this study, rice husk (RH), rice husk-derived materials, including rice ash (RHA), and Mobil Composition of Matter No. 41 (MCM-41) were evaluated as adsorbents for Hg(II) removal in aqueous systems. Among the tested materials, MCM-41 exhibited superior adsorption performance, achieving up to 98% Hg(II) removal under optimal conditions (pH 6.8, 3 g L⁻¹ of adsorbent, and a pollutant concentration of 0.90 mg L⁻¹). Adsorption followed a pseudo-second-order kinetic model and was best described by the Langmuir isotherm, indicating monolayer adsorption. The maximum adsorption capacity reached 0.80 mg g⁻¹. Thermodynamic analysis revealed that the process was spontaneous and exothermic, primarily governed by coordination interactions and hydrogen bonding with surface silanol groups. The adsorbent’s applicability was further assessed in distilled water, synthetic industrial wastewater, and river water. Although high removal efficiencies were maintained, a decrease was observed in complex matrices due to competition from coexisting ions. Reusability tests demonstrated that MCM-41 retained its performance over four adsorption cycles. Environmental safety was evaluated through ecotoxicological and microbiological assays. Daphnia magna exhibited high sensitivity to Hg(II) (EC₅₀ values of 0.0220 mg L⁻¹ at 24 h and 0.0158 mg L⁻¹ at 48 h), while treated samples showed improved germination indices of Lactuca sativa, particularly in distilled and river water. However, residual toxicity persisted in industrial wastewater matrices. Overall, rice husk-derived MCM-41 is a promising and sustainable adsorbent for Hg(II) removal, though further optimization is needed to mitigate residual toxicity in complex water matrices. Full article

Flue gas torrefaction is an emerging biomass pretreatment technology that utilizes industrial flue gas as a reactive medium to replace inert atmospheres. However, the intrinsic complexity of biomass and the catalytic interference of ash hinder mechanistic elucidation. This study investigated the torrefaction behavior of demineralized poplar wood under N₂, CO₂, dry flue gas (DFG), and wet flue gas (WFG) at 300 °C for 5–20 min. Thermogravimetric analysis combined with kinetic modeling (FWO, KAS, and CR methods) revealed that the apparent activation energy (E_α) varied non-monotonically with atmosphere oxidizability. Under N₂, the average E_α was 177 kJ/mol following the three-dimensional diffusion model (D5). CO₂ gave the highest average E_α (314 kJ/mol) with the Avrami–Erofeev nucleation model (A₁/₄). DFG and WFG significantly reduced the average E_α to 133 and 128 kJ/mol, respectively, both following the A₁/₃ model. Consistently, WFG yields the lowest char and the highest gas yield. XPS and FTIR analyses indicated that flue gas atmospheres, especially WFG, promoted deeper deoxygenation and aromatization of biochar. Tar composition underwent a noticeable transition from ketones to aldehydes and saccharides under flue gas conditions, with the most remarkable variation observed under WFG. Gaseous products were dominated by CO₂ under N₂ and by CO under CO₂, while DFG and WFG produced moderate and stable gas compositions. These findings demonstrate that flue gas torrefaction, particularly under WFG, effectively enhances biomass effectively upgrades biomass quality by regulating pyrolysis kinetics and product distribution, and demineralized biomass is a suitable intermediate model for mechanistic investigation. Full article

This study investigates the ternary co-pyrolysis of Soma lignite (SL), a low-rank Turkish coal with high ash content, with two agricultural residues: pectin-rich sugar beet pulp (SBP) and lignin-rich peanut shell (PS). The primary objective is to clarify how biomass structure and blend composition control synergistic interactions, and how co-pyrolysis can upgrade the fuel properties of a low-quality coal while valorizing agro-industrial waste. Four SL:SBP:PS blends (80:10:10, 60:20:20, 40:30:30, and 20:40:40 wt.%) were tested by non-isothermal thermogravimetric analysis at 10 ${}^{\circ }$C min${}^{-1}$ under nitrogen. Differential thermogravimetric curves were deconvolved into four pseudo-components representing pectin/hemicellulose, cellulose, lignin/early coal, and main coal/mineral fractions. Mass-based deviation indices ($\Delta W$) and rate-based deviations ($\Psi$) from the additive prediction were calculated in three temperature regions to detect synergy and antagonism. The results demonstrate that interactions are strongly composition-dependent. The 40:30:30 blend exhibits the most pronounced synergistic enhancement, with average $\Delta W$ values of approximately −0.94 wt.% and −1.05 wt.% in the 350–500 ${}^{\circ }$C and 500–650 ${}^{\circ }$C ranges, respectively, while the 60:20:20 blend shows antagonistic behavior across all regions. For the 40:30:30 blend, the calculated higher heating value increases from 11.21 to 14.74 MJ kg${}^{-1}$, reflecting a gradual upgrading of the feed-mixture composition by biomass loading. Overall, the findings indicate that combining a pectin-rich, fast-devolatilising biomass with a lignin-rich, slower-decomposing biomass at an intermediate coal loading can shift mass loss to lower temperatures. This combination also produces measurable non-additive behaviour within the experimental noise level. In addition, it improves several feed-mixture indicators that are relevant to sustainable energy recovery from lignite-dominated regions. Full article

In this study, salmon fish bone waste from the fish processing industry was converted into an inorganic ash filler by calcination and incorporated into an SLA-compatible photopolymer resin at 4, 8, and 12 wt.%. To compensate for filler-induced optical scattering and rheological changes, the printing parameters were systematically optimized, and the optimum conditions were identified as a layer thickness of 30 µm and an exposure time of 12 s. Tensile tests performed in accordance with ASTM D638 Type IV showed that fish bone ash significantly enhanced the tensile strength of the photopolymer matrix, increasing it from 24.8 MPa for the neat resin to 37.95 MPa at 12 wt.% filler loading. In contrast, increasing filler content reduced elongation at break and promoted a more brittle fracture response. Statistical evaluation using Welch ANOVA and Games–Howell post hoc analysis confirmed that filler loading had a statistically significant effect on tensile strength (p < 0.05). FTIR analysis revealed that the filler remained chemically stable within the matrix and that the interfacial interactions were predominantly physical rather than covalent. SEM observations indicated that low and medium filler loadings improved crack deflection and energy dissipation, whereas particle agglomeration at higher loading increased the tendency for brittle fracture. These findings demonstrate that fish bone ash can be used as a sustainable bio-waste-derived reinforcement to improve the mechanical performance of SLA photopolymer composites. Full article

In this study, we investigated the possibility of partially substituting wheat flour in bread-making technology with a by-product (rapeseed meal) obtained after pressing of rapeseed seeds used to obtain edible oil. The research was conducted within the context of sustainable food systems and circular bioeconomy strategies. Experiments were conducted using substitution rates of 10%, 20%, and 30% (RMW1, RMW2, and RMW3), as well as their corresponding breads (RMWB1, RMWB2, and RMWB3). The results reveal a notable improvement in the nutritional profile, correlated with the increase in RM. Indeed, significant increases were observed in protein content (up to 16.64% in flours and 14.19% in breads), fat content (up to 8.72% and 7.89%, respectively), and ash content (up to 2.30% and 2.85%, respectively), while carbohydrates decreased (down to 63.72 g/100 g in flours and 45.76 g/100 g in breads). Furthermore, the phytochemical profile was significantly enhanced, as reflected by the increased antioxidant capacity and elevated total polyphenol concentration, highlighting the functional potential of RM-enriched products. Water absorption increased from 55% to 61%, accompanied by a decrease in dough stability, suggesting modifications in the gluten network. Mixolab analyses indicated reduced viscosity and starch retrogradation, while physical bread properties, including porosity, elasticity, and H/D ratio, decreased with increasing substitution levels. Sensory evaluation revealed that a 10% RM substitution ensured optimal acceptability, whereas higher levels (30%) resulted in significant quality deterioration. From a sustainability perspective, the incorporation of RM contributes to the valorization of agro-industrial by-products, reducing waste streams and promoting resource efficiency. Partial substitution of wheat flour also has the potential to decrease reliance on primary agricultural inputs, thereby lowering the environmental footprint associated with cereal production. Additionally, the improved antioxidant profile may enhance product stability and shelf life, contributing to food loss reduction. In conclusion, an incorporation level of up to 20% provided the most suitable compromise between improved nutritional value, functional and technological properties, consumer acceptability, and sustainability considerations, thereby supporting the formulation of novel bakery products consistent with circular bioeconomy concepts and sustainable dietary approaches. Full article

Waste materials are abundant and often act as slow environmental contaminants, creating severe ecological challenges. With rapid industrialization, electricity demand has increased substantially, and in India, coal-based thermal power plants (TPPs) remain the dominant source of power generation. Coal combustion produces two major by-products: fly ash and bottom ash (BA). While fly ash is widely utilized in blended cements due to its pozzolanic nature, BA has received comparatively limited attention despite having similar chemical characteristics. Owing to its coarser particle size, BA shows strong potential as a substitute for natural river sand, the excessive extraction of which has led to severe resource depletion and sustainability concerns. Unlike previous studies that focused on single-source BA or limited performance evaluation, this study investigates the use of BA from multiple sources to develop resource-efficient bottom ash concrete (BAC). Concrete mixes containing 0%, 20%, 35%, and 50% BA as volumetric replacements of river sand were evaluated for their fresh, mechanical, durability, and microstructural properties. The results indicate that BA significantly influences concrete performance due to its porous structure. Among the investigated mixes, 35% river sand replacement with BA showed the most favorable performance for the specific materials and sources used in this study, achieving up to 17.46% higher compressive strength and up to 16.14% higher resistance to transport-related properties at 90 days. Microstructural analysis confirmed the formation of secondary C–S–H gel, which enhanced matrix densification. However, 50% replacement resulted in reduced performance. The findings demonstrate that BA can be effectively utilized in concrete at replacement levels of up to 35% as a sustainable substitute for river sand under the investigated material conditions. Full article

This study investigates the development of sustainable ceramic materials using industrial and agricultural waste from the Kyzylorda region of Kazakhstan. The research focuses on the combined use of local clay, ash from the Kyzylorda thermal power plant (TPP), and rice husk ash (RHA). Experimental investigations included the evaluation of chemical composition, linear and volumetric shrinkage, water absorption, bulk density, and compressive strength of ceramic samples fired at 950–1050 °C. Microstructural (SEM) and phase composition (XRD) analyses were performed to explain the observed behavior. The results showed that the optimal composition was 70% clay, 20% TPP ash, and 10% RHA, which demonstrated the highest compressive strength (15.45 MPa), reduced water absorption, and improved densification. The enhanced performance is attributed to partial vitrification and viscous-phase-assisted densification and the formation of crystalline phases such as mullite, cristobalite, and anorthite. The study confirms that the combined use of TPP ash and RHA enables effective recycling of local waste materials and improves the physical and mechanical properties of ceramic products. Full article

Liquid-phase mineralization of CO₂ using coal fly ash (CFA) is an efficient approach to permanent CO₂ sequestration. To address the low leaching efficiency of calcium ions (Ca²⁺) in carbon mineralization, this study systematically investigates the leaching performance and leaching mechanism of calcium ions from CFA by using a sequential alkaline-acid processing (i.e., alkaline activation followed by acid leaching). The effects of NaOH concentration, acid concentration, acid type (HCl/CH₃COOH), reaction time, and grinding duration on leaching efficiency are studied. The reaction products are characterized by X-ray diffraction (XRD) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). A kinetic model is proposed to analyze the reaction dynamics and leaching mechanisms. The results show that the maximum Ca²⁺ leaching efficiency for untreated CFA is 43.7% after 40-min acid leaching with 7 mol/L HCl and 1:1.5 S/L ratio. The leaching efficiency can be enhanced to 72.1% after 50-min alkaline activation with 11 mol/L NaOH. Grinding the CFA can further increase the leaching performance of Ca²⁺. It is shown that the leaching efficiency can be enhanced to 58.75% and 82.3% after 90-min grinding, respectively, for cases without and with 50-min alkaline activation using 9 mol/L NaOH. It is also shown that a peak leaching efficiency of 86.51% can be obtained when 8 mol/L CH₃COOH is used for the acid system. The mechanism for the enhancement of leaching efficiency is that both NaOH activation and mechanical grinding can break down the calcium and aluminum silicate vitreous matrix of CFA, facilitating calcium release. Ca²⁺ leaching performance exhibits two regimes. The leaching efficiency is significantly time-dependent in the first regime, and it remains almost constant in the second regime after the efficiency reaches a pseudo-maximum value. The contribution of this study is that a theoretical foundation is provided for enhancing the Ca²⁺ recovery from CFA, which makes it practical for large-scale CFA utilization and permanent CO₂ sequestration in industry applications. Full article

To mitigate the effects of climate change, the world must significantly reduce its reliance on fossil fuels to lower greenhouse gas emissions. The nuclear power and renewable energy sources, such as solar, wind, water, waste, and geothermal energy, emit minimal to no greenhouse gases or pollutants during operation. These sources are considered crucial for combating climate change and supporting sustainable development. However, the production of electricity, like most industries, generates waste. Comparisons show clear differences: fossil fuel plants produce the largest total waste mass (primarily combustion ash, flue gas desulfurization residues, and wastewater sludge), while nuclear facilities generate a minimal volume but high-activity spent fuel and long-lived radioactive materials. Solar PV systems generate significant end-of-life electronic waste and glass encapsulant, and wind turbines yield moderate composite blade residues. Hydropower sediment management and geothermal scaling contribute unique waste streams of local concern. Regardless of the energy source, responsible waste management is critical to minimize environmental impacts. This article explores the sustainability of low-carbon energy sources, specifically focusing on waste management with the aim of highlighting the need of implementing targeted strategies such as advanced recycling and material substitution in order to minimize environmental impacts and enhance the circularity of low-carbon energy systems. Full article

Vanadium tailings-based ceramsite (VT-Ceramsite), a type of porous ceramsite synthesized from vanadium tailings, was employed for the adsorption of fluoride ions from high-fluoride wastewater. This approach not only mitigates environmental pollution caused by industrial solid waste but also effectively removes fluoride contaminants from wastewater. The effects of vanadium tailings content, sintering temperature, and sintering time on the adsorption performance of the VT-Ceramsite were systematically investigated. Comprehensive characterizations via XRD, SEM, BET, and adsorption modeling reveal that fluoride sequestration by VT-Ceramsite is governed by the synergy between physical diffusion and chemical interactions. While the porous architecture provides essential transport pathways, the chemically active sites facilitate stable bonding. Future research will prioritize surface functionalization and tailoring strategies to augment the density of these active sites, thereby maximizing the adsorption potential for treating complex industrial effluents. The optimal preparation conditions were determined to be a ratio of 6.5:2.5:1 for vanadium tailings, fly ash, and kaolin, with a preheating temperature of 300 °C for 20 min and a sintering temperature of 900 °C for 20 min. In these conditions, the adsorption capacity for fluorine ions can reach 43.59 mg/g. VT-Ceramsite exhibited a specific surface area of 3.61 m²/g, hydrochloric acid solubility of 1.2%, and a void fraction of 48.68%, all parameters met national industrial standards. In addition, the leaching concentrations of heavy metals were found to be well below the limits specified in CJ/T 299-2008, indicating that the material poses no risk of secondary pollution. The study provides an economical, safe, and environmentally friendly route for the utilization of solid waste, and it offers a promising adsorbent for treating high-fluoride wastewater. Full article

Poorly soluble hydrophobic organic pollutants, such as indole and diethyl phthalate (DEP), are difficult to remove efficiently from complex industrial wastewater due to low solubility and competitive adsorption. In this study, low-rank coal-based activated cokes derived from Wanli long-flame coal and Zhaotong lignite were modified through a combined process of acid-washing pretreatment and trimethylchlorosilane (TMCS) grafting. The acid-washing step effectively removed ash and unblocked pores, increasing the specific surface area and pore volume of the optimized Zhaotong lignite-based sample by 43.7% and 53.3%, respectively. Subsequent TMCS grafting successfully introduced hydrophobic methyl groups onto the surface, significantly enhancing hydrophobicity. The water contact angles of the composite materials (acid-washed plus TMCS-grafted) increased to 127.3° and 139.7°, compared to 117.8° and 112.6° for the original samples. The modified adsorbent derived from Zhaotong lignite exhibited high adsorption capacities, reaching 139.47 mg·g⁻¹ for indole and 120.19 mg·g⁻¹ for DEP in single-component systems, representing an increase of 20.1% for indole and 28.7% for DEP compared to the unmodified adsorbent. More importantly, in a competitive system containing phenol at PH = 10, the materials demonstrated superior selectivity towards the target hydrophobic pollutants. The phenol removal rate was 65.97%, and the removal rates for indole and DEP increased sharply to 98.17% and 92.17%, respectively. This work provides a feasible strategy for the advanced treatment of complex organic wastewater using coal-based adsorbents, achieving a dual enhancement in both adsorption capacity and selectivity. Full article

In recent years, there has been an urgent need for integrated solutions to synergistically manage industrial solid waste stockpiling and CO₂ emissions. Single-component solid waste mineralization, such as those using only fly ash (FA) or carbide slag (CS), often encounters performance bottlenecks, typically characterized by a compressive strength of less than 2 MPa and a carbonation efficiency of under 10%. Furthermore, a systematic quantitative understanding of the synergistic interactions within multi-component systems remains absent. This study employs Response Surface Methodology to investigate the interactive effects of solid waste ratios, the water-to-solid ratio, and alkali content, aiming to elucidate the synergistic mineralization mechanism and overcome the bottlenecks of single solid waste mineralization. Under optimized conditions—specifically, 34% CS, 30% phosphogypsum (PG), a water-to-solid ratio of 0.48, and an alkali content of 27%—the system achieved a 7-day compressive strength of 3.5 MPa and a CO₂ mineralization efficiency of approximately 16%, representing a significant improvement over typical single solid waste mineralization materials. Microstructural and spectroscopic analyses indicate that CS serves a dual function as both a calcium source for CaCO₃ precipitation and an alkaline activator for FA. FA constructs a dense aluminosilicate network via pozzolanic reactions, while SO₄²⁻ released from PG promotes the formation of ettringite, facilitating efficient pore filling and early strength development. Additionally, it was observed that surface pores were filled with more products compared to the interior, forming a gradient pore structure that is dense on the outside and sparse on the inside. The AFt and silicate gel were identified as the key microstructural driver for the performance enhancement. This study not only explores the ternary synergistic mechanism of FA, CS, and PG but also provides a viable pathway for developing high-performance solid waste-based mineralization materials that combine mechanical properties with efficient CO₂ sequestration. Full article

The pollution of water, including salt and fresh water, has become an emergency problem. Pollutants come from different sources and have various characteristics, starting from industry and fertilizers used in agriculture, sewage related to human living, and other sources. Diverse sources of pollution require a comprehensive approach to water purification. One possible approach may be the use of appropriate sorbents. Currently, one of the most promising materials used is zeolites. This is because they can come from various sources, including waste raw materials such as fly ash, and, therefore, allow for the use of a circular economy approach. Moreover, these materials can be modified, which enables their selective use for selected types of pollutants. Eventually, these materials become economically viable options. The main aim of this article is to present and analyze possible solutions to water pollution based on zeolite materials. For this purpose, a critical literature review was prepared. The review reveals that zeolites perform particularly well in ion-exchange-driven removal of inorganic contaminants, while their effectiveness for organic micropollutants under realistic conditions is often limited. The identified trade-offs between removal efficiency, regeneration stability, and scalability indicate that zeolites are best applied as function-specific rather than universal sorbents. From a sustainability perspective, this targeted applicability is supported by advantages, such as low material cost, long service life, and the possibility of using naturally occurring or waste-derived precursors, which, together, enable resource-efficient water treatment processes, reduced reliance on energy-intensive technologies, and the valorization of industrial byproducts within circular economy frameworks. Full article

Tetracycline (TC) contamination in reservoirs poses environmental and human health risks, particularly antibiotic resistance in ecosystems. Bagasse fly ash (BFA), a by-product from the sugarcane processing industry, has gained attention as an environmentally friendly adsorbent. In this study, we aimed to investigate the mechanism of TC adsorption using batch experiments to evaluate the effects of various factors. For example, pH value ranged from 4 to 10, contact time varied between 0 and 90 min, adsorbent doses were noted as 0.5–2.5 g per 50 mL, the initial concentrations of TC were 10–40 mg/L, and the temperature ranged from 293.15 to 318.15 K. To perform surface characterization of BFA, we employed the scanning electron microscopy (SEM) technique. Based on the results of Fourier transform infrared spectroscopy (FTIR) and surface area analysis (Brunauer–Emmett–Teller; BET), its structure and chemical properties are favorable for TC adsorption. Our results demonstrate that the optimal conditions for adsorption were at pH 7.0 and 60 min contact time. The adsorption capacity tended to increase with the initial concentrations of TC and reached a maximum of 0.58 mg/g when the initial concentration was 40 mg/L. Our kinetic analysis results demonstrate that the pseudo-second-order model exhibited the best fit with the experimental data (R² = 0.95638); in comparison, the results of the isotherm behavior study using the Temkin model (R² = 0.97338) indicated the complex adsorption pathway on the BFA surface. Full article

This study develops a ternary Fe-based geopolymer system composed of metakaolin (MK), red mud (RM), and fly ash (FA) for the preparation of sustainable water-retaining subgrade materials for sponge-city roadbed applications. Unlike conventional formulations primarily designed for structural strength or rapid permeability, the proposed MK–FA–RM system was designed to improve water-storage capacity while maintaining adequate mechanical support and environmental compatibility. In this ternary system, MK provides highly reactive aluminosilicate species for geopolymer network formation, RM introduces Fe-bearing phases and enhances industrial solid-waste utilization, and FA contributes to particle packing, workability, and resource efficiency. A constrained ternary mixture design implemented using Design-Expert software was adopted to optimize precursor proportions. Within the investigated compositional range, the fitted first-order mixture model showed acceptable statistical adequacy for preliminary composition screening (R² = 0.86). The optimal blend (60% MK, 30% RM, and 10% FA) achieved a 7-day compressive strength of 8.37 MPa and a water retention rate of 35.3% under ambient curing conditions, satisfying the strength requirement considered for the target subgrade/base-layer application. Microstructural and phase analyses suggest that the synergistic interaction of the three precursors promoted Fe-modified aluminosilicate gel formation together with conventional geopolymer gel products, while improving matrix continuity and preserving interconnected pore space for water storage. This multiscale structural effect helps explain how the material achieved a balance between water retention capacity and mechanical support. Under the tested conditions, the material maintained acceptable residual strength after short-term exposure to water, acid, and sulfate-containing solutions. Life-cycle assessment indicated a 70% reduction in CO₂ emissions compared with ordinary Portland cement, while pilot-scale cost analysis showed a 39% lower production cost than MetaMax-based geopolymer materials. Pilot-scale application further demonstrated the constructability and water-regulation potential of the material in practical environments. Overall, the proposed ternary Fe-based geopolymer demonstrates that Fe-rich industrial wastes can be engineered into low-carbon and economically viable water-retaining subgrade materials that balance hydraulic regulation, structural adequacy, and sustainability. Nevertheless, long-term durability, cyclic loading performance, and direct nanoscale characterization of Fe-bearing gel evolution still require further investigation. Full article