Search Results (187)

To address the technical challenges in bisphenol A (BPA) pollution control, this research introduced a novel synthetic approach combining co-precipitation with subsequent thermal treatment to engineer layered double hydroxides (LDHs) with a spinel-structured CoMn-LDO catalyst. Systematic material characterizations such as a scanning electron microscope (SEM), an X-ray diffractometer (XRD), a transmission electron microscope (TEM), and X-ray photoelectron spectroscopy (XPS) were employed to analyze the structural and chemical properties of the synthesized CoMn-LDO calcined at 500 °C. The catalytic performance was evaluated under optimized conditions (35 °C, pH 7.0, 2.0 mM PMS, 0.3 g/L catalyst), and mechanistic studies were conducted to identify the dominant reactive oxygen species. The CoMn-LDO exhibited exceptional peroxymonosulfate (PMS) activation performance, achieving 96.75% BPA degradation within 90 min and 58.22% TOC removal. The synergistic redox cycling between Co²⁺/Co³⁺ and Mn³⁺/Mn⁴⁺ promoted the generation of ·OH (72.3% contribution) and SO₄·⁻. The catalyst demonstrated superior stability, maintaining 89% degradation efficiency after five cycles. These results provide theoretical and practical insights for developing high-efficiency persulfate-activating catalysts. Full article

Biocatalytic nanomembranes have emerged as promising platforms for micropollutant remediation, yet their practical application is hindered by limitations in removal efficiency and operational stability. This study presents an innovative approach for fabricating highly stable and efficient biocatalytic nanomembranes through the co-immobilization of horseradish peroxidase (HRP) and glucose oxidase (GOx) within a covalent organic framework (COF) nanocrystal. Capitalizing on the dynamic covalent chemistry of COFs during their self-healing and self-crystallization processes, we achieved simultaneous enzyme immobilization and framework formation. This unique confinement strategy preserved enzymatic activity while significantly enhancing stability. HRP/GOx@COF biocatalytic membrane was prepared through the loading of immobilized enzymes (HRP/GOx@COF) onto a macroporous polymeric substrate membrane pre-coated with a polydopamine (PDA) adhesive layer. At HRP and GOx dosages of 4 mg and 4.5 mg, respectively, and a glucose concentration of 5 mM, the removal rate of bisphenol A (BPA) reached 99% through the combined functions of catalysis, adsorption, and rejection. The BPA removal rate of the biocatalytic membrane remained high under both acidic and alkaline conditions. Additionally, the removal rate of dyes with different properties exceeded 88%. The removal efficiencies of doxycycline hydrochloride, 2,4-dichlorophenol, and 8-hydroxyquinoline surpassed 95%. In this study, the enzyme was confined in the ordered and stable COF, which endowed the biocatalytic membrane with good stability and reusability over multiple batch cycles. Full article

Developing efficient and recyclable periodate (PI)-based advanced oxidation processes (AOPs) for the removal of emerging organic pollutants (EOPs) has attracted considerable attention. However, the structure–activity relationship of single-atom catalyst in PI-AOP systems remains poorly understood. In this study, a hollow carbon-supported single-Fe atom catalyst (HCFe800) was synthesized and applied for PI activation toward bisphenol A (BPA) degradation. Under neutral pH and ambient temperature, HCFe800 enabled complete removal of BPA within 1 min, achieving a degradation rate constant (k) of 5.094 min⁻¹—approximately 3 and 10 times higher than that of Fe-free and solid control catalysts, respectively. After normalization, the apparent degradation rate constant was 1–3 orders of magnitude greater than those of previously reported catalysts. The optimized Fe doping amount and pyrolysis temperature facilitated the formation of atomically dispersed FeN₄ sites, which outperformed Fe clusters and iron oxides in catalytic activity. The hollow porous structure further enhanced the exposure of active sites, contributing to the exceptional performance. The HCFe800/PI system remained highly effective across broad pH (3–7) and temperature (5–35 °C) ranges and in the presence of 100-fold concentrations of common inorganic ions. Mechanistic studies revealed that the main reactive species were ¹O₂, O₂^•−, and IO₃^•, with negligible involvement of high-valent Fe species. Eight less-toxic BPA degradation products were identified. Moreover, the system was extendable to various other EOPs and exhibited excellent recyclability via thermal regeneration. This work provided fundamental insights into designing and applying single-atom catalysts for PI-based advanced treatment of EOPs. Full article

Herein, carbon nanofiber (CNF) was prepared by pyrolyzing electrospun cellulose nanofiber, which was further used to incorporate with graphitic carbon nitride (g-C₃N₄) to prepare metal-free photocatalyst (CNF/g-C₃N₄). CNF/g-C₃N₄ was then used to degrade bisphenol A (BPA) under visible light with the assistance of peroxymonosulfate (PMS). It was illustrated from the results that CNF with conjugated aromatic structure could significantly enhance the light absorption range and capability. At the existence of PMS, 0.5 g/L of CNF/g-C₃N₄ could efficiently degrade 0.05 mM of BPA within 45 min with a high total organic carbon removal rate of >70% under visible light. It was found that the reaction system could generate various reactive oxygen species (ROSs) including hydroxyl radical, superoxide radical and singlet oxygen for BPA degradation. Due to the existence of these species, the reaction system exhibited high performance adaptability towards abundant water matrices and high stability under consecutive runs. This work prospects a new strategy to develop a high-performance advanced oxidation system for quick organic pollutant degradation and mineralization. Full article

Herein, we rationally designed a molecular catalytic filter for effective micropollutants decontamination via peroxymonosulfate (PMS) activation. Specifically, iron phthalocanine (FePc) molecules with defined Fe–N₄ coordination were immobilized onto carbon nanotubes (CNTs), forming a hybrid catalyst that integrated molecular precision with heterogeneous catalytic properties. The resulting CNT-FePc filter achieved a 98.4% removal efficiency for bisphenol A (10 ppm) in a single-pass operation system, significantly outperforming the CNT/PMS system without FePc (41.6%). Additionally, the CNT-FePc/PMS system demonstrated remarkable resistance to performance inhibition by common water matrix components. Unlike typical radical-dominated PMS activation processes, mechanistic investigations confirmed that the CNT-FePc/PMS system selectively promoted singlet oxygen (¹O₂) generation as the primary oxidative pathway. Density functional theory (DFT) calculations revealed that PMS exhibited stronger adsorption on FePc (−3.05 eV) compared to CNT (−2.86 eV), and that FePc effectively facilitated O–O bond elongation in PMS, thereby facilitating ¹O₂ generation. Additionally, seed germination assays indicated a significant reduction in the biotoxicity of the treated effluents. Overall, this work presents a catalyst design strategy that merges molecular-level coordination chemistry with practical flow-through configuration, enabling rapid, selective, and environmentally benign micropollutant removal. Full article

Removal of micropollutants using biological treatment systems remains a challenge, since conventional bioprocess systems require adaptations to provide more advanced treatment. An ambient temperature upflow anaerobic sludge blanket (UASB) reactor was employed, followed by a two-stage (saturated and unsaturated) vertical subsurface flow (VSSF) constructed wetland (CW) system, to treat domestic wastewater from a nearby settlement and investigate the occurrence and fate of 10 contaminants of emerging concern (CECs) in decentralized, non-conventional treatment systems. The integrated UASB—two-stage CW system achieved high performance regarding abatement of target CECs across all periods. Removal efficiencies ranged from 78% ± 21% (ketoprofen) to practically 100% (2-hydroxybenzothiazole). The pilot system was found to be robust performance-wise and provided enhanced treatment in comparison to a conventional wastewater treatment plant operating in parallel. Most of the target CECs were successfully treated by UASB, saturated and unsaturated CWs, while ibuprofen, bisphenol A and diclofenac were mostly removed in the unsaturated CW. Environmental risk assessment revealed that triclosan poses a significant ecological risk to algae during treated wastewater disposal into the aquatic environment. Additionally, cumulative risk quotient indicated that the potential for mixture toxicity should be carefully considered across all trophic levels. Full article

Objective: To evaluate the cytotoxicity and endocrine-disrupting potential of materials used in removable orthodontic retainers. Methods: A literature search (2015–2025) covered in vitro cytotoxicity, estrogenicity, in vivo tissue responses, and clinical biomarkers in PMMA plates, thermoplastic foils, 3D-printed resins, PEEK, and fiber-reinforced composites. Results: Thirty-eight in vitro and ten clinical studies met inclusion criteria, identified via a structured literature search of electronic databases (2015–2025). Photopolymer resins demonstrated the highest cytotoxicity, whereas thermoplastics and PMMA exhibited predominantly mild effects, which diminished further following 24 h water storage. Bisphenol-type compound release was reported, but systemic exposure remained below regulatory limits. No statistically significant mucosal alterations or endocrine-related effects were reported in clinical studies. Conclusions: Retainer materials are generally biocompatible, though data on long-term endocrine effects are limited. Standardized biocompatibility assessment protocols are necessary to enable comparative evaluation across diverse orthodontic materials. Single-use thermoplastics contribute to microplastic release and pose end-of-life management challenges, raising concerns regarding environmental sustainability. Full article

Steroid hormones are micropollutants that contaminate water worldwide and have significant impacts on human health and the environment, even at very low concentrations. The aim of this article is to provide an overview of technologies for the removal of endocrine-disrupting compounds with a focus on oestrogens (estrone E1, 17β-oestradiol E2, estriol E3), the synthetic oestrogen (17α-ethinylestradiol EE2 and bisphenol A BPA), and pharmaceuticals found in wastewater. Hormonal and pharmaceutical contaminants are mostly persistent organic compounds that cannot be easily removed using conventional wastewater treatment processes. For this reason, researchers have tried to develop more efficient tertiary wastewater treatment technologies to reduce micropollutant concentrations in wastewater. This review covers the following processes: Advanced oxidation, nanofiltration, ultrasound, electro-Fenton processes, electrolysis, adsorption, ozonation, photolysis, photocatalysis, ultrafiltration, and electrocoagulation. Attention was paid to the effectiveness of the processes in terms of eliminating hormones and pharmaceuticals from wastewater, as well as on economic and environmental aspects. The combination of different processes can be a promising treatment scheme for retaining and degrading hormonal and pharmaceutical compounds from wastewater. With hybrid technologies, the advantages of the methods are combined to maximise the removal of pollutants. However, optimal methods of wastewater treatment depend on the quality and quantity of the wastewater, as well as the residual hormonal and pharmaceutical compounds and their hazardous effects. Full article

The immobilization of a laccase from Pycnoporus sanguineus UEM-20 via the formation of cross-linked enzyme aggregates (CLEAs) was optimized through a central composite design (CCD) of response surface methodology (RSM). Both free and immobilized enzymes were investigated for their physico-chemical characteristics, and their adequacy in removing bisphenol A (BPA) and decolorizing malachite green dye in solution was evaluated. The immobilization caused only minor differences in thermostability. Upon immobilization, the enzyme experienced some changes in its kinetic properties. The V_max decreased by a factor of 1.1, and the K_M increased by a factor of 1.89. These kinetic changes did not modify in any remarkable way the capacity of the immobilized enzyme in degrading BPA and decolorizing malachite green dye. Its sensitivity to NaCl was also minimally affected by immobilization. However, its sensitivity to sodium sulfate was substantially decreased. After 1 month’s conservation, the activity of the free form had suffered a drastic drop. The immobilized form, by contrast, remained 100% active after 6 months. All these findings predict that the immobilized laccase from P. sanguineus UEM-20 may be useful in the enzymatic bioremediation of pollutants such as endocrine disruptors and synthetic dyes. Full article

Rapid industrialization has escalated environmental pollution caused by organic compounds, posing critical challenges for wastewater treatment. Advanced oxidation processes based on peroxymonosulfate (PMS) suffer from metal leaching and catalyst recycling challenges. To address these limitations, this study developed a nitrogen-doped biochar aerogel (NBA) derived from poplar wood powder as an eco-friendly and easily recoverable PMS activator. The NBA catalyst, optimized by tuning the calcination temperature to achieve a specific surface area of 297.5 m² g⁻¹, achieved 97% bisphenol A (BPA) removal within 60 min with a catalyst dosage of 0.3 g/L and 1.0 mM PMS under mild conditions. The material exhibited broad pH adaptability (pH 3.5–9), recyclability (>94% efficiency after thermal treatment), and versatility in degrading seven pollutants (BPA, phenol, 4-chlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol, rhodamine 6G, and levofloxacin) through synergistic radical (•OH, SO₄^•−, O₂^•−) and non-radical (¹O₂) pathways. X-ray photoelectron spectroscopy (XPS) analyses revealed that nitrogen doping enhanced PMS activation by optimizing electronic structures. This study highlights the potential of waste biomass-derived carbon aerogels as eco-friendly, efficient, and reusable catalysts for advanced oxidation processes in wastewater treatment. Full article

Bisphenol A (BPA) is an industrial chemical used primarily in the manufacture of polycarbonate plastics and epoxy resins. BPA is considered an endocrine-disrupting chemical (EDC) because it interferes with hormonal systems. Over the decades, several techniques have been proposed for BPA removal in wastewaters. This study discusses recent advancements and progress of effective techniques for BPA removal, including membrane, adsorption, advanced oxidation process (AOPs), and biodegradation. The mechanisms of BPA adsorption on modified adsorbents include pore-filling, hydrophobic interactions, hydrogen bonding, and electrostatic interactions. Among the various agricultural waste adsorbents, Argan nut shell-microporous carbon (ANS@H20–120) exhibited the highest efficiency in removing BPA. Furthermore, the performance of magnetic treatment for activated carbon (AC) regeneration is introduced. According to the present study, researchers should prioritize agricultural waste-based adsorbents such as ACs, highly microporous carbons, nanoparticles, and polymers for the removal of BPA. In particular, the combination of adsorption and AOPs (advanced oxidations) is regarded as an efficient method for BPA removal. A series of relevant studies should be conducted at laboratory, pilot, and industrial scales for optimizing the application of agricultural waste-based AC to reduce BPA or other refractory pollutants from an aqueous environment. Full article

Substantial amounts of nitrogenous (N) compounds, as well as bisphenol A (BPA) and bisphenol S (BPS), contribute to the impurities of pharmaceutical contamination (PC) in wastewater, which have detrimental effects on the environment, humans, and aquaculture. The anammox processes is primarily used to treat wastewater contamination, in which certain microbial communities play a crucial role. In this regard, the present study focuses on microbial communities and the functional genes involved in the anammox process. Further, the current study highlights the secondary (biological) and tertiary (advanced) methods; these techniques are more effective solutions for PC treatment. Anammox bacteria are the primary drivers of the wastewater’s ammonium and nitrite removal process. However, overall, 25 anammox species have been recognized between five important genera, including Anammoxoglobus, Anammoximicrobium, Brocadia, Kuenenia, and Jettenia, which are mainly found in activated sludge and marine environments. The group of bacteria called anammox has genes that encode enzymes such as hydrazine synthase (HZS), hydrazine dehydrogenase (HDH), nitrite oxidoreductase reductase (NIR), hydroxylamine oxidoreductase (HAO), and ammonium monooxygenase (AMO). The anammox process is responsible for developing about 30% to 70% N gases worldwide, making it a critical component of the nitrogen cycle as well. Therefore, this review paper also investigates the pathways of hydrazine, an intermediate in the anammox process, and discusses the potential way to significantly decrease the N-compound contamination from wastewater systems and the environmental effects of determined organic contaminants of BPA and BPS. Full article

Bisphenol A is a widely recognized endocrine disruptor that persists in ecosystems, harms aquatic organisms, and contributes to ecological degradation, raising global environmental concerns. Numerous studies have explored β-cyclodextrin–based adsorbents for Bisphenol A removal; however, their regeneration remains a major challenge, often relying on energy-intensive processes and excessive use of organic solvents. In this study, Bisphenol A was selected as a model pollutant, and its adsorption onto β-cyclodextrin nanosponges was investigated. After adsorption, Bisphenol A was efficiently recovered from the saturated β-cyclodextrin nanosponges using an innovative and sustainable supercritical CO₂-based green process, which simultaneously regenerated the adsorbent. The adsorption process achieved an efficiency of 95.51 ± 0.82% under optimized conditions (C₀ = 150 mg/L, m_β-CDNS = 0.15 g, T = 25 °C, and N = 200 rpm), with a maximum adsorption capacity of 47.75 ± 0.28 mg/g. The regeneration process achieved over 99% efficiency at 60 °C and 300 bar, with 10% (v/v) ethanol as a co-solvent, nearly fully restoring the adsorbent’s performance. Unlike conventional regeneration techniques, this green approach eliminates the need for environmentally harmful organic solvents while preserving the adsorbent’s structural integrity, making it a highly efficient and sustainable alternative. This study is the first to demonstrate the effective application of supercritical CO₂-based regeneration for β-cyclodextrin nanosponges in Bisphenol A removal, providing a scalable and environmentally sustainable solution for wastewater treatment. Furthermore, characterization analyses confirmed that the adsorbent retained its chemical and morphological stability after adsorption and regeneration. Full article

The comonomer bisphenol A (BPA) finds applications in the plastics industry, where it is used in the production of polycarbonates, plastics, PVC, thermal paper, epoxy and vinyl ester resins, and polyurethane. The water, with which many of these materials come into contact, is one of the main sources of human exposure to BPA. When ingested or touched, BPA can damage organs, disrupt the endocrine and immune systems, generate inflammatory responses, and be involved in genotoxic processes. Therefore, the need to develop effective techniques for removing BPA from aqueous environments is imperative. This paper provides a comprehensive review regarding the effective removal of BPA from water, focusing on the performance and adsorption mechanisms of various adsorbents based on chitosan and chitosan composites. The chemical and physical factors, adsorption kinetics and models governing the adsorption process of BPA in chitosan materials are also examined. This review outlines that, despite considerable progress in the absorption of bisphenol using chitosan gels, further research is necessary to assess the efficacy of these adsorbents in treating real wastewater and in large-scale manufacture. Full article

The biogas residue (BR) from the anaerobic digestion of sludge poses a threat to the environment due to the presence of toxic and hazardous substances. Furthermore, emerging contaminants, such as bisphenol A (BPA), are widespread in domestic and industrial wastewater, requiring efficient and sustainable treatment technologies. In this study, the BR-based biochar was pyrolyzed from urea-modified BR and employed as a catalyst to activate peroxymonosulfate (PMS) for BPA degradation. With BR-based biochar pyrolyzed at 750 °C as a catalyst, 20 mg/L of BPA was completely removed. Free radical detection confirmed that hydroxyl radical (•OH) and sulfate radical (•SO₄⁻) generation decreased with the increase in catalyst reuse times. The X-ray photoelectron spectra showed that the catalyst deactivation mainly resulted from -COOH and C-OH group loss, which acted as active sites for generating •OH and •SO₄⁻, and HCl or NaOH regeneration for catalysts could recover oxygen-containing functional groups, boosting BPA removal from 54.7% to 91.5% and 100%, respectively. Thermal regeneration could only enlarge the catalyst’s specific surface area (SSA) to recover adsorption capacity, but might not restore the free radical generation capability. This research offered a theoretical basis for the sustainable utilization of BR and provided a reference for reusing catalysts in wastewater treatment. Full article