Search Results (2,378)

To address the inherent drawbacks of peroxymonosulfate advanced oxidation processes (PMS-AOPs), including the low efficiency of reactive species production, short radical half-lives, and restricted pollutant degradation performance, sodium salt-assisted modification was adopted to fabricate ZIF-8-derived carbon. In this study, sodium salt-assisted modification was adopted to treat ZIF-8, and the chlorine-doped derived carbon materials HNC-T_x-Cl were prepared for peroxymonosulfate activation and tetracycline degradation in water. Compared with NC-800 fabricated by direct calcination of ZIF-8 at 800 °C, HNC-800-Cl synthesized via NaCl-assisted calcination exhibits more abundant pore structures and richer carbon defects, with a specific surface area of 1115 m²/g and a high graphitic defect ratio I_D/I_G of 1.20. Catalytic tests reveal that HNC-800-Cl achieves 93.39% tetracycline removal within 90 min at a catalyst dosage of 0.05 g L⁻¹ and PMS concentration of 0.1 mM. The system possesses a strong anti-interference ability toward complex water environments, maintaining a favorable degradation performance in the presence of coexisting anions, natural organic matter and actual water matrices. It also exhibits outstanding cycling stability, retaining a removal rate of 80.34% after five recycling runs. Radical quenching experiments and EPR characterization verify that superoxide radical (·O₂⁻) is the dominant reactive species during tetracycline degradation. Both the radical and non-radical pathways are clarified to illustrate the mechanisms of PMS activation and pollutant degradation. This work provides a novel catalytic material strategy to overcome the deficiencies of conventional PMS-AOPs, and offers a new perspective for structural regulation and non-metallic doping modification of ZIF-8-derived carbon materials. Full article

The persistence of refractory organic pollutants (e.g., antibiotics) in aquatic environments necessitates efficient and sustainable remediation strategies. In this study, a circular economy approach was adopted to convert iron sludge into a value-added carbon residue (CR) composite via one-step co-pyrolysis. The resulting material was designed as dual-functional, enabling synergistic pollutant removal through adsorption and catalytic oxidation. Experimental results demonstrated that the CR composite effectively adsorbed and degraded organic pollutants. The primary adsorption sites were attributed to surface functional groups, porous structure, and electrostatic interactions. Meanwhile, iron species, surface functional groups, and persistent free radicals facilitated the generation of singlet oxygen (¹O₂) and hydroxyl radicals (·OH), which in turn promoted pollutant degradation. The CR/PDS system exhibited excellent performance in real wastewater remediation, which was attributed to the high interference resistance of ¹O₂. Furthermore, the application of CR did not pose any significant environmental risk in aqueous solutions. Taken together, these findings present a novel material for pollutant removal and provide a cost-effective strategy for the valorization of waste iron sludge. Full article

This article systematically reviews the structural characteristics of layered double hydroxides and biochar (LDHs/biochar) composites, summarizes the features and optimization strategies of preparation methods such as coprecipitation, hydrothermal synthesis, ball milling, and calcination–reconstruction, analyzes their adsorption performance and mechanisms in controlling various water pollutants including organic contaminants, heavy metals, and nutrients, and provides insights into future research trends and practical applications, aiming to offer references for improving material performance and promoting practical use. The existing research results show that LDHs/biochar composites exhibit good application potential for various pollutants, such as dyes, antibiotics, heavy metal ions, and phosphates. The coprecipitation method is simple and easy to operate, and the LDHs/biochar composites prepared by this method exhibit favorable adsorption performance, with potential for industrial-scale production. The mechanisms of pollutant removal by LDHs/biochar composites primarily include electrostatic attraction, ion exchange, hydrogen bonding, complexation, and π–π electron interactions. Both the biomass type and the LDH type influence the adsorption performance of the composites. Therefore, designing LDHs/biochar composites based on pollutant characteristics and adsorption mechanisms is key to achieving effective pollution control. Currently, research on target pollutant-oriented material design and material regeneration remains underdeveloped and requires further breakthroughs. Full article

High-frequency ultrasound-assisted activation of peracetic acid (PAA) was investigated as a tunable advanced oxidation process for the removal of organic pollutants from water. Sunset Yellow FCF (SSY), a representative anionic azo dye, was used as a probe contaminant in a 425 kHz sonoreactor to clarify the roles of PAA speciation, acoustic cavitation, dissolved gases, oxidant dose, acoustic power, and initial pH. UV spectroscopic analysis showed that PAA exhibits pH-dependent far-UV absorbance associated with acid-base speciation and peroxide equilibria, while ultrasonication promoted simultaneous PAA activation and H₂O₂ accumulation. Compared with PAA alone and ultrasound alone, the combined US/PAA process markedly enhanced SSY decolorization. Under natural conditions, 5 mg/L SSY and 5 mM PAA were completely decolorized within 210 min, with an initial rate of 0.116 mg/L·min, compared with 0.078 and 0.0086 mg/L·min for ultrasound and PAA alone, respectively. The corresponding synergy ratio and synergy index were 1.5 and 1.34. The process exhibited tunable reaction-pathway control, with two favorable pH windows: a strongly acidic region, where interfacial HO^•-driven sonochemistry and PAA stability are favored, and a mildly alkaline region, where PAA deprotonation promotes peracetate-driven acyl/peroxyl radical-chain propagation. Oxygen saturation improved performance, whereas CO₂ suppressed cavitation-driven activation. Increasing PAA concentration and acoustic power enhanced removal up to practical limits, beyond which radical scavenging and diminishing sonochemical returns became evident. Beyond demonstrating enhanced decolorization, this study distinguishes US/PAA from previously reported UV/PAA, transition-metal/PAA, and ultrasound-only systems by showing how 425 kHz cavitation converts PAA into a tunable hybrid HO^•/acyl–peroxyl radical network. The main contribution is a mechanistic operating map that links PAA speciation, sonochemical peroxide accumulation, dissolved gas chemistry, acoustic power, oxidant dose, and pH to pollutant-removal performance, thereby defining practical windows for sono-activated PAA treatment of anionic dyes and related recalcitrant contaminants. Full article

In this study, Prunus dulcis hull (PDH) has been used to develop a cost-effective and eco-friendly adsorbent material for the removal of Pb²⁺ ions from polluted waters. The PDH particles were characterized using various techniques, including ATR-FTIR spectroscopy, ion-selective electrode ISE-H⁺ potentiometric titrations, pH of point of zero charge (pH_pzc) analysis, thermogravimetric analysis (TGA), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX). Single-batch adsorption experiments were conducted at different pH values, with pH 5.0 identified as the optimal initial pH in terms of Pb²⁺ adsorption performance of PDH. The study also evaluated the effects of temperature, ionic medium, and several organic ligands with different functional groups on the adsorption capacity of PDH. The results showed that PDH is an effective adsorbent for lead ions, with adsorption capacities (q_m) ranging from 43 to 101 mg g⁻¹ and an adsorption equilibrium time of approximately 750 min at room temperature. Additionally, column adsorption experiments demonstrated that PDH can be reused at least four times with minimal loss in performance. The adsorption behavior of PDH was comparable under both equilibrium (batch) and non-equilibrium (column) conditions, with the breakthrough time (BT₀.₅) values significantly affected by the background salts present in the toxic metal ion solution. Full article

This study investigates the feasibility of utilizing locally sourced Nicotiana tabacum biomass from Adıyaman, Türkiye, as a cost-effective biosorbent for the removal of copper and chemical oxygen demand (COD) from industrial wastewater originating from the Adıyaman Organized Industrial Zone. Batch adsorption experiments were conducted to systematically investigate the influence of solution pH, contact time, and initial metal concentration on adsorption performance. The untreated wastewater exhibited elevated pollution levels, with mean chemical oxygen demand and copper concentrations of 925 ± 391 mg/L and 2.54 ± 0.97 mg/L, respectively. Four tobacco-derived biosorbents (Çelikhan, Ova, Bulam, and Çağlan) were evaluated under optimized experimental conditions (pH ≈ 8.3, 60 min contact time, and a biosorbent dosage of 2.2 g/L). The Çelikhan biosorbent exhibited the highest copper removal efficiency (approximately 83%), whereas chemical oxygen demand removal ranged between 28% and 34%. The adsorption kinetics were well described by the pseudo-second-order model, with coefficients of determination ranging from 0.987 to 1.000. Isotherm analysis further indicated favorable adsorption behavior, with a maximum Langmuir adsorption capacity of 1.867 mg/g. Fourier transform infrared (FT-IR) spectroscopy confirmed the involvement of hydroxyl, carbonyl, and ester functional groups in metal binding. These findings highlight tobacco biomass as a sustainable and cost-effective biosorbent for industrial wastewater treatment. This study presents the first comprehensive evaluation of locally sourced Adıyaman tobacco biomass as a biosorbent for the removal of copper and organic pollutants from real industrial wastewater, integrating kinetic, isotherm, and FT-IR analyses to elucidate the underlying adsorption mechanisms. Full article

Chlorinated benzoquinones such as 2,6-dichlorobenzoquinone (DCBQ) are toxic disinfection by-products that may persist in treated waters, requiring post-treatment strategies. In this study, the photo-Fenton process was evaluated for DCBQ degradation, with a focus on the influence of pH on kinetics, oxidation behavior, and water quality evolution. Experiments were conducted using 50.0 mg/L DCBQ, 1.0 mg/L Fe²⁺, and 2.0 mM H₂O₂ under UV irradiation (150 W) within a pH range of 3.0–12.0. Degradation followed apparent second-order kinetics, with maximum rates at acidic pH. At initial pH 3.0–5.0, rapid pollutant removal was accompanied by efficient aromaticity (UV₂₅₄) and color elimination, intense dissolved oxygen consumption, transient turbidity peaks due to intermediate formation, and increases in total dissolved solids, indicating extensive oxidation and a high degree of organic matter transformation, as inferred from indirect physicochemical indicators. At near-neutral pH, oxidation was slower, with delayed aromatic and chromophoric decay and moderate accumulation of intermediates. Mildly alkaline conditions exhibited limited radical activity, stable turbidity, and reduced mineralization. Under strongly alkaline conditions, oxidation was largely inhibited, with persistent aromaticity and negligible oxygen consumption. These findings highlight the importance of integrating advanced oxidation processes with adsorption-based systems for efficient and sustainable water treatment of emerging contaminants. Full article

Nanotechnology offers transformative potential for wastewater treatment, yet its full-scale implementation remains bottlenecked by the “lab–reality gap”. While bench-scale studies using idealized matrices report outstanding pollutant removal efficiencies, performance routinely deteriorates in authentic wastewater due to complex matrix interferences, natural organic matter (NOM) competitive binding, fouling dynamics, and unpredictable nano–bio transformations. Moving beyond traditional reviews that focus heavily on material synthesis and theoretical capacities, this review provides a novel, systems-oriented, and function-driven perspective on environmental nanotechnology. We critically evaluate the operational stability and behavior of nano-enabled systems under realistic conditions, categorizing nanomaterial roles into reactive interfaces, selective barriers, signal generators, and biological modulators. Crucially, this work examines the synergistic integration of nanotechnology with advanced oxidation processes (AOPs), membrane bioreactors, and digital intelligence—including artificial intelligence (AI) and real-time nanosensing—to achieve smart fouling management and circular resource recovery. Finally, we propose a comprehensive, multidimensional evaluation framework that simultaneously assesses technical efficiency, stability, scalability, economic feasibility, environmental safety, and system compatibility. This review delivers a pragmatic roadmap to bridge the chasm between isolated laboratory discovery and robust, sustainable, field-scale wastewater engineering. Full article

The limited energy efficiency of sonochemical processes and the high reagent consumption of Fenton-based treatments remain the major challenges for large-scale water treatment. This study investigates a hybrid Sono–Galvano–Fenton (US/GF) process for the degradation of malachite green as a model organic pollutant, using parallel and series coupling configurations for the assessment of the potential synergistic effects of ultrasound and galvanic Fenton reactions. The results show that acoustic streaming can effectively replace mechanical stirring, providing comparable mixing performance while reducing mechanical energy requirements by approximately 20–30%. In addition, in situ sonochemical hydrogen peroxide generation contributes to pollutant degradation, achieving up to 35–50% removal efficiency, although this remains lower than the efficiency obtained with conventional Galvano–Fenton processes, which typically achieve removal efficiencies of 70–90%. In addition, continuous-flow hybrid configurations appear promising to improve in situ reagent production and overall process efficiency. Full article

De novo granulation of autochthonous microorganisms of water and wastewater reduces the start-up periods for cultivating aerobic granular sludge (AGS) and enrichment of degrading strains. However, it has not been demonstrated using refractory carbon compounds. This work investigated the formation of AGS from the seawater microbiome and establishment of pollutant removal pathways by feeding acetonitrile as the sole carbon and nitrogen source. Use of acetonitrile at an organic loading rate of 0.124 kg/m³/day enabled rapid emergence of aggregates and then stable granules (size: 1.3 mm; SVI5: 68 mL/g) within two weeks. TOC removal accompanied by ammonium nitrogen release was consistent and stable at 93% during the 50 days of bioreactor operation. Formation of acetamide and ammonium indicated involvement of nitrile hydratase and amidase enzymes in acetonitrile biodegradation. Ammonium released during acetonitrile biodegradation was removed by partial nitrification and the nitrite denitrification pathway. However, incomplete ammonium removal led to accumulation of up to 120 mg/L NH₄⁺-N by day 50. Phosphate was removed via the enhanced biological phosphate removal pathway. This study shows that de novo granulation permits cultivation of AGS via the de novo granulation approach for simultaneous biodegradation of refractory acetonitrile and biological nutrient removal under saline conditions. Full article

In the treatment of high-salinity wastewater, the removal of nitrogen and organic pollutants remains a challenge, while the production of value-added compounds, such as ectoine from halophilic bacteria, offers a promising resource recovery pathway. In this study, halophilic activated sludge enriched with Thauera as the dominant strain was cultivated in a sequencing batch reactor (SBR) to treat synthetic high-salinity wastewater (30 g/L NaCl) under different sludge retention times (SRTs). The optimal nitrogen and organic carbon removal performances were achieved at an SRT of 10 days, with an ammonia nitrogen removal rate of 77.67% and a total organic carbon (TOC) removal rate of 72.51%. Ectoine production was strongly SRT dependent, as volumetric ectoine concentration was ~2 mg/L at 5 d SRT, almost undetectable at 10 d SRT, ~10 mg/L at 16 d SRT, and peaked at 21.5 mg/L at 22 d SRT. Short SRTs favored dynamic ectoine utilization for osmoprotection and metabolic stability, whereas long SRTs led to passive ectoine accumulation and deteriorated treatment performance. The system realized stable short-cut heterotrophic nitrification with negligible nitrite and nitrate accumulation, indicating direct conversion of ammonia to gaseous nitrogen. These results demonstrate that SRT regulation effectively balances ectoine synthesis and pollutant removal, providing a feasible strategy for resource-oriented treatment of high salinity wastewater. Full article

Accurate prediction of contaminant transport and self-purification processes in rivers remains challenging because pollutant dispersion, biochemical reactions, and hydrodynamic conditions interact across multiple spatial scales. This study aims to develop and compare mathematical models for soluble contaminant transport and biodegradable organic matter removal in channels and rivers. Unsteady advection–diffusion–reaction equations were formulated for one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) transport scenarios and solved through numerical techniques based on the transformation of partial differential equations into systems of ordinary differential or algebraic equations. In parallel, the classical Streeter–Phelps model and an extended formulation incorporating turbulent diffusion were implemented to evaluate organic load degradation and oxygen deficit dynamics. Simulations were performed using a Matlab R2019a-based computational framework under representative hydraulic and reaction conditions obtained from literature data and empirical correlations. The results showed that, under specific conditions, the 3D model reproduced trends comparable to those predicted by the 2D model, while the latter approached the behavior of the 1D formulation. The Streeter–Phelps model predicted an organic load removal efficiency of 97.74%, a purification index of 1.9564, a critical time of 18.43 h, and a critical distance of 6.93 km. These findings provide a useful framework for river water-quality assessment and support future applications involving complex hydrodynamic and pollutant-loading scenarios. Full article

Traditional electro-Fenton systems for chlorinated antibiotic wastewater suffer from low mineralization, catalyst deactivation, and secondary pollution caused by chloride ions. In this work, nitrogen-functionalized graphite felt cathodes were synthesized by electrodeposition-pyrolysis. Pyridinic N and graphitic N were identified by XPS. The obtained cathodes were employed in a metal-free electro-Fenton system for effective tetracycline (TC) removal and mineralization. The results show that the optimal electrode (N-GF-3) achieved 93% degradation efficiency and 73% mineralization of TC in 60 min, when the optimized conditions (pH = 3 and current density = 20 mA/cm²) were employed. Unusually, with the presence of Cl⁻, the system showed even higher catalytic performance, having a degradation kinetic constant 2.4 times higher than that without chloride. The electrode was also reusable, maintaining a TC degradation efficiency above 90% in the fifth cycle. Based on fluorescence analysis of ·OH, a possible dual-path reaction mechanism is proposed. This mechanism provides new insights into designing advanced oxidation processes for the treatment of complex chlorinated organic wastewater. Nevertheless, the potential formation of chlorinated byproducts requires additional investigation. Full article

Eutrophication remains a persistent water-quality problem in shallow lakes, where external inputs interact with internal loading and biogeochemical cycling. Although floating treatment wetlands (FTWs) are increasingly promoted as nature-based solutions for water remediation, their field-scale interpretation in hydrologically complex eutrophic lakes remains challenging. This study examined the spatial organization of water quality during the operation of a floating-island system in a eutrophic urban lake affected by polluted tributary inflow. The study was not designed to quantify isolated FTW removal efficiency, but to evaluate spatial water quality organization during FTW operation under real-use field conditions. Water quality was monitored over two growing seasons across six functionally defined zones, and spatial and temporal patterns were analyzed using descriptive statistics and linear mixed-effects models. The results showed parameter-specific spatial structuring rather than a uniform treatment response. The clearest inlet-lake contrasts were observed for electrical conductivity (EC), suspended matter (SM), and nitrate nitrogen (NO₃-N), whereas biochemical oxygen demand (BOD₅), ammonium nitrogen (NH₄-N), and total organic carbon (TOC) showed lower values at the inlet and higher values in downstream zones. Dissolved oxygen (DO), oxygen saturation (SO), chemical oxygen demand (COD), nitrite nitrogen (NO_2-N), and orthophosphate phosphorus (PO₄-P) showed moderate or non-robust zonal effects. These findings indicate that FTWs in shallow eutrophic lakes should be evaluated through functional zoning and parameter-specific interpretation rather than as isolated units with uniform removal responses. Full article

Azo dyes are a major cause of environmental pollution, but under lab-based conditions can be removed using a coupled adsorption and electrochemical oxidation process; the Nyex Rosalox™ (NR) process. However, wastewater effluents are more complex than tap water, indicating that there is a need to assess how altered effluent conditions affect the adsorption of azo dyes onto the adsorbent used (Nyex™ 2000) and overall removal efficiency of the NR process. Analysis indicates that higher temperatures, the addition of minor amounts of sodium chloride, or acidification increased adsorption, while the presence of dissolved organic carbon (DOC) only showed a minor impact if compared to baseline tap water conditions and appears to be dye-specific. Analyses further indicated that effluent conditions could have a major impact on the overall dye removal efficiency using the NR process, with up to 48% more being removed during acidic or saline conditions and, to a lesser extent, when DOC was present. Increased temperature or alkalinity had minimal impact, with inconsistent results across the dyes assessed. Combined, this highlights that effluent-specific conditions can have a major impact on the removal efficiency and should be considered during the planning stage of the azo dye treatment process. Full article