Search Results (259)

Despite its broad application due to its affordability, biodegradability, and natural antimicrobial and antioxidant activities, chitosan (CS) still exhibits limitations in mechanical strength and barrier effectiveness. Owing to its unique chemical characteristics, itaconic acid (IT) presents potential as a compatibilizing agent in polymeric blend formulations. Biodegradable polymers composed of chitosan (CS), itaconic acid (IT), and starch (S) were synthesized using two polymerization methods. The first method involved grafting IT onto CS at varying ratios of IT (4%, 6%, and 8% wt.), using 1% v/v acetic acid/water as the solvent and potassium persulfate as the initiator. In the second approach, starch (S) was blended with the copolymer P(CS-g-IT) at concentrations of 1%, 3%, and 5%, utilizing water as the solvent and glacial acetic acid as a catalyst. The resulting biodegradable films underwent characterization through FTIR, TGA, SEM, and mechanical property analysis. To further explore the effects of combining IT, starch, and carbon black, the blends, referred to as P[(CS-g-IT)-b-S], were also loaded with carbon black. This allowed for the evaluation of the materials’ physicomechanical properties, such as viscosity, tensile strength, elongation, and contact angle. The findings demonstrated that the presence of IT, starch, and carbon black collectively improved the films’ mechanical performance, physical traits, and biodegradability. Among the samples, the blended copolymer with 1% starch exhibited the highest mechanical properties, followed by the grafted copolymer with 8% IT and the blended copolymer mixed with carbon black at 7%. In contrast, the blended copolymer with 5% starch showed the highest hydrophilicity and the shortest degradation time compared to the grafted copolymer with 8% IT and the blended copolymer mixed with 7% carbon black. Full article

In this study, sulfur-doped biochar (SBC) was successfully synthesized using peanut shells as the raw material and sulfur powder as the sulfur source. The composition, structural characteristics, and catalytic performance of SBC in the degradation of phenol via persulfate (PDS) activation were systematically investigated. Characterization results demonstrate that the prepared SBC exhibited a typical lamellar structure with abundant pores and fissures on its surface. XPS analysis confirmed the successful incorporation of sulfur into the biochar matrix, primarily in the form of thiophene. Under the optimized condition of a 20% sulfur doping ratio, the SBC exhibited high efficiency in activating PDS, achieving a phenol degradation rate of 97%. Remarkably, the removal rate remained at 81% even after the fifth cycle, indicating excellent cyclic stability. Density functional theory (DFT) calculations and electrochemical impedance spectroscopy (EIS) measurements further revealed that sulfur doping significantly modified the electron density distribution of the biochar, reducing its surface electrochemical impedance from 32.88 Ω to 13.64 Ω. This reduction facilitated efficient electron transfer during the catalytic process. This study provides both experimental and theoretical insights into the charge distribution characteristics of sulfur-doped biochar, offering valuable references for understanding the mechanism of PDS activation by SBC. Full article

This study explores biochar-based catalysts made from hardwood (HW) and wheat straw (WS) biomass for activating persulfate (PS) in the removal of lindane and β-endosulfan from water. The effects of pyrolysis temperature, solution pH, and PS concentration were investigated. The results indicated that both feedstock and pyrolysis temperature are key factors influencing biochar composition. Biochars pyrolyzed at 700 °C exhibited higher surface areas compared to those pyrolyzed at 400 °C, suggesting more effective interactions with the target pesticides. Changes in pH had a minimal impact on pesticide removal, while increasing the PS concentration from 0.5 to 3 mM accelerated degradation. However, further increases in PS concentration slowed the degradation of both pesticides. Under optimal conditions (pH of 7.0 ± 0.2 and PS concentration of 3 mM), the HW700/PS and WS700/PS systems achieved > 90% removal of pesticides within 4 h. Quenching experiments confirmed that non-radical species (¹O₂), generated through persulfate activation by biochar, were the key factor in lindane degradation in both systems, supporting the catalytic role of biochar rather than mere adsorption. In the HW700/PS system, SO₄^•−, HO^•, and ¹O₂ acted synergistically to enhance the degradation of β-endosulfan, whereas in the WS700/PS system, the degradation was mainly driven by SO₄^•− and ¹O₂. Notably, HW700 biochar maintained its activation efficiency during β-endosulfan degradation even after five cycles. This research offers new insights into the potential of biochar-activated PS as a green, cost-effective, and efficient method for water treatment, addressing pesticide-contaminated surface water and promoting agricultural waste recycling. Full article

Organic soil pollution poses a persistent threat to environmental sustainability by disrupting nutrient cycling and ecosystem functioning. The biochar-activated persulfate (PS)-based advanced oxidation process (AOP) has emerged as a promising strategy for the sustainable remediation of organic-contaminated soils. This review provides a comprehensive overview of the recent progress in the PS-based degradation of organic pollutants, with a particular focus on the role of biochar as an efficient and environmental activator. This review further summarizes advancements in the design of modified biochars, including metal (Fe, Cu, Co, Mn, Zn, and La), non-metal (N, S, B, P), and functional group modifications, aimed at enhancing the PS activation efficiency while minimizing secondary environmental risks. Importantly, the overlooked contributions of soil microorganisms in PS/biochar systems are discussed, highlighting their potential to complement chemical oxidation and contribute to eco-compatible remediation pathways. This review emphasizes the sustainability-oriented evolution of PS/biochar technology, highlighting the importance of a cost-efficient implementation, ecological compatibility, and the rational engineering of smart, regenerable catalysts. These insights support the advancement of PS/biochar-based AOPs toward scalable, intelligent, and environmentally sustainable soil remediation. Full article

Sludge-derived biochar (SDB) synthesized by the pyrolysis of sludge is gaining enormous interest as a sustainable solution to wastewater treatment and sludge disposal. Despite the proliferation of general biochar reviews, a focused synthesis on SDB-specific advances, particularly covering the recent surge in multifunctional wastewater treatment applications (2020–2025), receives little emphasis. In particular, a critical analysis of recent trends, application challenges, and future research directions for SDB is still limited. Unlike broader biochar reviews, this mini-review highlights the comparative advantages and limitations of SDB, identifies emerging integration strategies (e.g., bio-electrochemical systems, catalytic membranes), and outlines future research priorities toward enhancing the durability and environmental safety of SDB applications. Specifically, this review summarized the advances from 2020 to 2025, focusing exclusively on functional modifications, and practical applications of SDB across diverse wastewater treatment technologies involved in adsorption, catalytic oxidation, membrane integration, electrochemical processes and bio-treatment systems. Quantitative comparisons of adsorption capacities (e.g., >99% Cd2+ removal, >150 mg/g tetracycline adsorption) and catalytic degradation efficiencies are provided to illustrate recent improvements. The potential of SDB in evaluating traditional and emerging contaminant degradation among the Fenton-like, persulfate, and peracetic acid activation systems was emphasized. Integration with membrane technologies reduces fouling, while electrochemical applications, including microbial fuel cells, yield higher power densities. To improve the functionality of SDB-based systems in targeting contamination removal, modification strategies, i.e., thermal activation, heteroatom doping (N, S, P), and metal loading, played crucial roles. Emerging trends highlight hybrid systems and persistent free radicals for non-radical pathways. Despite progress, critical challenges persist in scalability, long-term stability, lifecycle assessments, and scale-up implementation. The targeted synthesis of this review offers valuable insights to guide the development and practical deployment of SDB in sustainable wastewater management. Full article

N-Nitrosodimethylamine (NDMA) is a widely recognized disinfection by-product that poses significant carcinogenic risks in drinking water. Conventional methods for NDMA removal, such as nanofiltration and reverse osmosis membranes, have limited efficacy due to NDMA’s small molecular weight and polar properties. Advanced oxidation processes (AOPs) have shown promise, but traditional Fenton processes often fall short due to the chemical structure of nitrosamines in NDMA. This study proposes a novel, cost-effective approach using a one-step carbonization method to synthesize a catalyst from ferric ammonium citrate (FAC). The resulting FAC-600 integrates zero-valent iron and iron carbide with carbon-based functional groups, enhancing catalytic and electron transport activities. Our experiments demonstrated that the FAC-600/persulfate (PS) AOP system achieves over 90% NDMA removal across a wide concentration range (50 μg L⁻¹ to 1000 μg L ⁻¹) with a limited dosage of 0.5 g L⁻¹. Mechanistic insights revealed that superoxide and hydroxyl radicals dominate NDMA degradation, facilitated by the presence of dissolved oxygen and PS. This study underscores the potential of the FAC-600/PS AOP system as a robust and efficient solution for NDMA removal, promising safer drinking water through practical application. Full article

The functionalization of nitrogen-doped graphene with β-Cyclodextrin (designated β/N-rGO) was employed to enhance the dispersibility of graphene materials and to establish an adsorption-catalytic oxidation system using peroxymonosulfate (PMS) for the removal of trace antibiotics from water. The experimental results indicated that β-Cyclodextrin was effectively dispersed on the support structure of nitrogen-doped graphene, which enhanced the specific surface area and dispersibility of the material. The adsorption-catalytic oxidation system comprising β/N-rGO and PMS degraded 92.35% of sulfamethoxazole within 12 min and exhibited significant removal efficiency for sulfonamides, quinolones, macrolides, tetracyclines, β-lactams, and chloramphenicol antibiotics across a pH range of 3–12. The reaction time was reduced by over 10% compared to the unmodified material, with a more pronounced improvement in treatment efficiency, particularly under low-pH conditions. The activation energy of β/N-rGO was estimated to be approximately 4.5 kJ/mol, and elevated temperatures accelerated the reaction, with the removal rate remaining above 85% after five regeneration cycles. Quenching experiments and EPR spectra confirmed that the primary pathway for PMS activation by β/N-rGO was a non-radical process dominated by singlet oxygen. These findings broaden the research and application scope of cyclodextrin–graphene interactions and provide a feasible approach for the removal of trace antibiotics from water. Full article

Intensive industrial activities have led to severe polycyclic aromatic hydrocarbon (PAH) contamination of adjacent lands. Remediating such contaminated soil is crucial for maintaining long-term ecological health and sustainable development. This study systematically assessed the performance of a microwave-activated persulfate (MW/PS) oxidation method in remediating pyrene-contaminated soil. Under conditions of 80 °C and a persulfate concentration of 23.8 mg/g, this system achieved 85.3% pyrene degradation within 30 min, significantly outperforming both single microwave and thermal-activated persulfate (TH/PS) systems. Key factors influencing the oxidation efficiency included the temperature, persulfate and pyrene concentrations, moisture, and humic acid content. An electron paramagnetic resonance analysis confirmed the generation of reactive oxygen species, including ^•OH, SO₄^•− and ¹O₂, in the MW/PS system, while O₂^•− was exclusive to the TH/PS system. However, further experiments revealed that ¹O₂ had a negligible impact on pyrene degradation, suggesting that its role may have been overestimated in previous studies. The high MW/PS performance was attributed to the synergistic effects of both thermal and non-thermal (molecular vibration) mechanisms. Based on these findings, the pathways of pyrene degradation were proposed, with intermediate products exhibiting reduced toxicity and bioaccumulation potential. This study provides valuable insights into the application of MW/PS systems in the remediation of PAH-contaminated soils. Full article

To address the issues of poor Co²⁺ regeneration and limited interfacial electron transfer in heterogeneous catalytic systems, this study proposes the synthesis of highly efficient and stable Co₃O₄/ZnO composites through the pyrolysis–oxidation reaction of Co/Zn MOFs for the degradation of rhodamine B (RhB) using activated peroxymonosulfate (PMS). The results confirmed that the catalyst exhibited a high electron transfer capacity, and the synergistic effect between the bimetals enhanced the reversible redox cycle of Co³⁺/Co²⁺. Under optimal conditions, complete removal of RhB was achieved in just 6 min using the Co₃O₄/ZnO composite, which demonstrated excellent stability after five cycles. Furthermore, the catalyst exhibited a high degradation efficiency in real water samples with a total organic carbon (TOC) removal rate of approximately 65% after 60 min. The electrochemical measurements, identification of active species, and X-ray photoelectron spectroscopy (XPS) analysis revealed that non-radicals (¹O₂ and direct charge transfer) played a major role in the degradation of RhB. Finally, the potential mechanisms and degradation pathways for RhB degradation using this catalyst were systematically investigated. This study opens new avenues for the development of efficient and stable PMS catalysts, and provides insights into the preparation of other emerging metal oxides. Full article

Coke (AC) was modified and activated with sodium hydroxide (NaOH) and potassium hydroxide (KOH) to produce AC-Na and AC-K, respectively, and applied as a persulfate (PS) activator to promote phenol (Ph) removal in water. Under the given experimental conditions, compared to AC/PS (Ph removal effect was 77.09%), the Ph removal effects were 94.46% and 88.73% for AC-K/PS and AC-Na/PS, respectively. AC-K proved to be a more effective activator than AC-Na and was used for all the subsequent experiments. When PS/phenol molar ratio was 6.26:1:00, the initial system pH was 7 and the system temperature was 25 °C; the AC-K/PS system could effectively remove Ph (98.75%) from the simulated wastewater. After that, the stability of AC-K was verified. Electron paramagnetic resonance (EPR) and quenching analysis confirmed the hydroxyl free radical (•OH) to be predominant within this system. EPR combined with X-ray photoelectron spectroscopy (XPS), Fourier-transformed infrared (FTIR) spectroscopy, and Raman spectroscopy indicated that the sulfate radical (SO₄^•−) and •OH were generated due to the defects in AC-K, thereby enhancing the PS activation potency of AC-K. Additionally, the radical quenching experiments showed that the superoxide (O₂⁻) radical is a key intermediate product promoting SO₄^•− and •OH, which aided Ph removal. Both radical (SO₄^•− and •OH) and non-radical (¹O₂) pathways were found to co-exist during the removal process. The Ph removal rate of the AC-K/PS system could still reach 29.50%, even after four repeated cycles. These results demonstrate that the unique AC-K/PS system has a potential removal effect on organic pollutants in water. Full article

This study examines the use of a1 mm-diameter tubular microreactor submerged in a temperature-controlled water bath to activate potassium persulfate (KPS) via thermal, Fe²⁺-catalyzed, and combined thermo-catalytic processes for degrading the persistent textile dye Safranin O (SO). The efficiency of these methods was evaluated under varying conditions, including KPS, dye, and Fe^2⁺ flow rates, solution pH, reactor length, and water matrix quality (deionized water, tap water, seawater, and secondary effluent from a wastewater treatment plant (SEWWTP)) across bath temperatures of 30–80 °C. Total organic carbon (TOC) analysis validated the results. Maximum dye conversion (up to 89%) occurred at 70 °C, with no improvement beyond this temperature, mainly due to radical-radical recombination. Longer reactors (2–6 m) enhanced conversion, though this effect diminished at higher temperatures due to efficient thermal activation. Increasing dye flow rates reduced removal efficiency, particularly above 50 °C, highlighting kinetic and mass transfer limitations. Persulfate flow rate increases improved conversion, but a plateau emerged at 80 °C. At lower temperatures (30–40 °C), Fe²⁺ addition significantly boosted SO conversion in deionized water. Between 40 and 50 °C, conversion rose from 30.27% (0 mM Fe²⁺) to 85.91% (0.2 mM Fe²⁺) at 50 °C. At higher temperatures (60–80 °C), conversion peaked at 70 °C for lower Fe²⁺ concentrations (100% for 0.01–0.05 mM Fe²⁺), but higher Fe²⁺ levels (0.1–0.2 mM) caused a decline above 60 °C, dropping to 68.44% for 0.2 mM Fe²⁺ at 80 °C. Deionized, tap, and mineral water showed similar performance, while river water, secondary effluent, and seawater inhibited SO conversion at lower temperatures (30–60 °C). At 70–80 °C, all matrices achieved efficiencies comparable to deionized water for both thermal and thermo-catalytic activation. The thermo-catalytic system achieved >50% TOC reduction, indicating significant organic matter mineralization. The results were comprehensively analyzed in relation to thermal and kinetic factors influencing the performance of continuous-flow reactors. Full article

Global industrialization has intensified the emission of emerging contaminants (ECs), posing a serious threat to the environment and human health. Persulfate-based advanced oxidation processes (PS-AOPs) have become a research hotspot due to their efficient degradation capability and environmentally friendly features; carbon-based materials are ideal catalysts for activating persulfate (PS) due to their tunable electronic structure, abundant active sites, and low cost. This study summarizes the application of carbon-based materials (graphene, single-atom catalysts (SACs), etc.) in PS-AOPs, and provides insights into the degradation mechanisms of radicals (e.g., sulfate radical (SO₄^−·), hydroxyl radical (·OH)) and non-radicals (e.g., ¹O₂(singlet oxygen), electron transfer). The removal efficacy of carbon-based catalysts for antibiotics, phenols, and dyes was compared, and the key degradation pathways were elucidated. In addition, the activation of PS can be accelerated, and catalytic efficiency can be improved by synergizing with ancillary technologies (e.g., light, electricity). Despite the great potential of carbon-based catalysts, their large-scale application is limited by the complexity of the catalyst preparation process and the lack of selectivity for complex water qualities. Future studies can accelerate the practical application of PS-AOPs in wastewater treatment through the precise design of SACs and the construction of multi-mechanism synergistic activation systems. Full article

The removal of polychlorinated dibenzo-p-dioxins (PCDDs) via advanced oxidation processes (AOPs) poses a significant challenge due to their high toxicity and chemical stability. In this study, a series of well-dispersed cobalt nanoparticles supported on carbon nitrides (xCoCNs) was synthesized to activate peroxymonosulfate (PMS) for 2,8-dichlorodibenzo-p-dioxin (2,8-DCDD) degradation under visible light. The catalysts prepared were characterized using SEM, XPS, photoluminescence (PL), and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). Among them, 2CoCN with an optimal Co content exhibited the highest photocatalytic efficiency, achieving 90.5% degradation of 2,8-DCDD within 160 min under visible light/persulfate oxidation (Vis+PMS+2CoCN system). Compared with other catalysts, 2CoCN exhibited superior optical performance and a narrower bandgap, enabling efficient excitation under visible light (Vis). Notably, all xCoCNs demonstrated pH adaptability, achieving complete degradation of 2,8-DCDD under neutral conditions (pH = 7) without additional acid/alkali adjustment. Through rigorous free radical capture experiments, it was demonstrated that SO₄^•−, ^•OH and ¹O₂ were the primary reactive oxygen species (ROS) in the Vis+PMS+2CoCN system. The catalyst exhibited excellent reusability, with stable activity retained over five cycles. Based on these findings, degradation pathways and mechanisms of 2,8-DCDD in the 2CoCN+Vis+PMS system were proposed. This study presents an effective approach for PCDD abatement in wastewater treatment applications. Full article

Membrane-based persulfate catalysis technology offers a dual approach to wastewater treatment by facilitating both physical separation and chemical oxidation. This innovative method significantly enhances pollutant removal efficiency while mitigating membrane fouling, positioning it as a promising advanced oxidation technology for wastewater management. This review comprehensively examines the critical aspects of material design, activation mechanisms, and technological challenges. Membrane materials and structures are crucial for enhancing the overall efficiency of the technology. By analyzing various catalytic materials and modification strategies, the study reveals the intricate interactions between membrane structures, catalytic performance, and pollutant degradation. The clear mechanism of pollutant degradation is the key to achieve accurate degradation. The research highlights three primary activation pathways: free radical, non-radical, and hybrid mechanisms, each offering unique advantages in addressing complex water contamination. Finally, the future challenges and research directions are put forward. Despite remarkable progress, challenges remain in membrane stability, economic feasibility, and large-scale implementation. Therefore, this study outlines the latest materials, mechanisms, and prospects of membrane-based persulfate technology, which are expected to promote its widespread application in environmental governance. Full article

Polyethylene microplastics (PE MPs) pose a severe threat to aquatic ecosystems and human health, demanding urgent, sustainable remediation strategies. While the electro-Fenton process is widely used for treating refractory pollutants in wastewater, its standalone application remains inadequate for PE MPs due to their stable chemical structure and complex molecular chains. This study introduces a green and sustainable magnetite-activated persulfate electro-Fenton (Mt-PS-EF) system designed to address these limitations while aligning with circular-economy principles. By synergizing Fe₃O₄ catalysis, persulfate activation, and electrochemical processes, the Mt-PS-EF system achieves efficient PE MP degradation through hydroxyl (·OH) and sulfate (SO₄·⁻) radical-driven oxidation. Under optimized conditions (60 mg/L PE, 40 mM persulfate, 150 mg Fe₃O₄, 20 h treatment), a 90.6% degradation rate was attained, with PE MPs undergoing chain scission, surface erosion, and release of low-molecular-weight organics. Crucially, the magnetic property of magnetite facilitated the recovery and reuse of the catalyst, significantly reducing material costs and minimizing waste generation. By integrating catalytic efficiency with resource recovery, this work advances scalable, eco-friendly solutions for microplastic pollution mitigation, directly contributing to UN Sustainable Development Goals (SDGs) 6 (Clean Water) and 14 (Life Below Water). The findings highlight the potential of hybrid electro-Fenton technologies in achieving sustainable wastewater treatment and plastic waste management. Full article