Search Results (149)

Pharmaceuticals and personal care products (PPCPs), as persistent organic pollutants, are widely present in various aquatic environments. Their long-term presence in aquatic environments poses a potential threat to ecosystems and human health. This study established an efficient, green, and cost-effective photocatalytic method using P25 titanium dioxide (P25TiO₂) to simultaneously degrade five representative PPCPs (methyl paraben (MeP), carbamazepine (CBZ), bisphenol A (BPA), diclofenac (DFC), and triclosan (TCS), while elucidating the reaction mechanisms. Under sunlight irradiation, degradation rates for all five PPCPs reached 100%, achieving near-complete mineralization with total organic carbon (TOC) removal rates exceeding 95%. This demonstrates the system’s exceptional capability to not only degrade the parent compounds but to thoroughly convert them into benign inorganic substances. We systematically investigated the effects of catalyst concentration, initial pollutant concentration, light intensity, pH, and various common inorganic anions (chloride, sulfate, bicarbonate, phosphate) and humic acid (HA) on the degradation process. Additionally, mechanistic studies indicated that hydroxyl radicals (·OH) are the primary active species in the system. The degradation rate differences among various persistent organic pollutants (DFC > BPA > TCS > CBZ > MeP) primarily stem from variations in the reactivity of different functional groups within their molecular structures toward ·OH. In summary, this study provides a promising and practical solution for treating complex medical wastewater containing five typical PPCPs. Full article

Metal packaging materials remain fundamental across food, beverage, pharmaceutical, cosmetic, and technical sectors owing to their combination of mechanical robustness, total light and gas barrier performance, thermal resistance, and established recyclability. Aluminum alloys, tinplate, tin-free steel (TFS/ECCS), stainless steels, metal–matrix composites (MMCs), and metal–polymer or metal–paper laminates define distinct metal-based packaging architectures whose metallurgical and interfacial design governs forming behaviour, corrosion and migration pathways, coating integrity, and mechanical reliability. In this review, these architectures are examined from a materials- and systems-oriented perspective, linking composition, microstructure, processing routes, and surface engineering to functional performance across rigid, semi-rigid, and flexible formats. The analysis also considers the ongoing transition from bisphenol A (BPA)-based epoxy linings to BPA-free and hybrid coating chemistries, the use of nano-structured metallic and metal-oxide surfaces, and the role of composite laminates in which thin metallic foils are combined with polymeric or paper-based structural layers. These material and architectural aspects are discussed together with safety, regulatory, and circularity considerations that increasingly influence the design and selection of metal-based packaging. Ion migration, coating degradation, and corrosion under realistic storage environments are considered in relation to EU, FDA, ISO, and sector-specific requirements, while attention is also paid to the contrast between well-established closed-loop recycling infrastructures for aluminum and steel and the more complex end-of-life management of coated metals and multilayer laminates. The review provides a unified framework connecting materials selection, metallurgical design, processing, performance, regulatory compliance, and sustainability in metal-based packaging systems. Applications spanning consumer goods, pharmaceuticals, cosmetics, and advanced electronics are integrated to support an overall understanding of how metallic and hybrid metal-based architectures underpin functional reliability and life-cycle sustainability. Full article

Plastics are highly persistent materials, and their environmental degradation can potentially exacerbate, rather than alleviate, pollution. The degradation of plastic materials releases toxic monomers and additives, such as bisphenol A (BPA), styrene, and dioxins, which are more reactive, harmful, and persistent than intact plastics. With half-lives ranging from weeks to decades, they bioaccumulate in food chains, disrupt ecosystems, and contribute to endocrine disruption and mutagenicity. Natural degradation pathways, like microbial metabolism and photodegradation, are slow and incomplete, often leaving toxic intermediates such as microplastics. Artificial strategies, including bioremediation and advanced oxidation processes (AOPs), show potential to address the problems of plastic pollution but face additional challenges like secondary pollution and scalability. Sustainable alternatives, including bioplastics and renewable non-plastic substitutes, present promising solutions. However, their widespread adoption is hindered by challenges such as high production costs and the need for specific conditions to facilitate degradation, necessitating further research and development. A combined approach of reducing plastic production, advancing recycling, and implementing effective remediation strategies is critical to mitigating plastic pollution’s long-term impacts on ecosystems, biodiversity, and human health. This review provides a critical analysis of the current understanding of plastic degradation processes and the toxic byproducts they generate. It highlights the paradox wherein increased degradability may exacerbate environmental hazards. Additionally, the review assesses innovative, eco-friendly alternatives designed to mitigate plastic pollution. Full article

In this study, exfoliated mica nanoparticle particles were utilized to reduce the band gap of mica nanoparticles, and the loading of ZnO and BiOCl enhanced the photocatalytic performance. Within the mica nanosheets, exfoliation led to a decrease in band gap energy from 7 eV to 2.5 eV, thereby improving the semiconductor properties of the material. It is more suitable for photocatalysis research and the improvement in photocatalytic capabilities. This research prepared exfoliated mica nanoparticle particles (eMica) via ultrasonic exfoliation combined with CTAB intercalation and acid treatment. Subsequently, a ZnO/BiOCl ternary composite photocatalyst supported on eMica (ZnO/BiOCl@eMica) was synthesized using a hydrothermal method. The crystal structure, chemical composition, morphology, and optical properties of the materials were systematically characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier-transform infrared spectroscopy (FT-IR). The effects of reaction conditions (ZnO/BiOCl molar ratio, catalyst dosage, initial BPA concentration, and solution pH) on photocatalytic performance were investigated through BPA degradation experiments. The results showed that when the molar ratio of eMica:ZnO:BiOCl was 1:3:3, the catalyst dosage was 0.1 g/50 mL, the initial BPA concentration was 20 mg/L, and pH = 10, the composite achieved a BPA degradation efficiency of 98% within 30 min. Free radical trapping experiments confirmed that superoxide anions (·O₂⁻), hydroxyl radicals (·OH), and holes (h⁺) were the primary active species. The excellent performance of the composite is attributed to the high specific surface area and electron transfer capability of eMica, as well as the synergistic charge separation effect of the ZnO/BiOCl heterojunction. Furthermore, the composite maintained nearly 80% degradation efficiency after four cycles, demonstrating good stability and practical potential. Two-dimensional (2D) mica nanoparticles open new opportunities for exploring the photocatalytic properties of 2D materials and show promise in the field of 2D photocatalysis. Full article

BNCT (Boron Neutron Capture Therapy) is a binary radiotherapeutic modality in which high LET (Linear Energy Transfer) particles are generated from ¹⁰B(n,α)⁷Li reaction, ideally within boron-loaded tumour cells, so the therapeutic outcome depends critically on the pharmacokinetics and biodistribution of boron carriers. In this review, boron-containing agents for BNCT, with a focus on ADMET (absorption, distribution, metabolism, excretion and toxicity) and model-informed design, were examined. Low-MW (low-molecular-weight) compounds, peptide conjugates, polymeric and nanostructured platforms and cell-based vectors were surveyed and how physicochemical properties, transporter engagement and nano–bio interactions govern tumour uptake, subcellular localisation and normal tissue exposure were discussed. A shift from maximising boron content towards optimising exposure profiles using PET (Positron Emission Tomography), PBK (physiologically based pharmacokinetic) modelling and in silico ADMET tools to define irradiation windows was also discussed. Classical agents such as BPA (Boronophenylalanine) and BSH (Sodium Borocaptate) are contrasted with newer polymeric and metallacarborane-based carriers, with attention to brain penetration, endosomal escape, linker stability, biodegradation and elimination routes, as well as platform-specific toxicities. Incontestably, further progress in BNCT will highly depend on integrating imaging-derived kinetics with PBPK-informed dose planning and engineering subcellularly precise yet degradable carriers, and that ADMET-guided design and spatiotemporal coordination are central to achieving reproducible clinical benefit from BNCT’s spatial selectivity. Full article

The growing volume of decommissioned wind turbine blades, primarily made of glass fibre-reinforced polymers (GFRP), poses major recycling challenges. This study explores a microwave (MW)-assisted thermochemical recycling to recover high-quality fibres from GFRP waste. Two routes were evaluated: (i) a dry route using direct MW heating, and (ii) a semi-wet route involving solvent pre-swelling followed by microwave pyrolysis. The dry route suffered from poor heating due to GFRP’s inherently low dielectric loss, whereas the semi-wet route enabled more effective resin degradation. Five swelling agents were tested: acetic acid (AcOH), hydrogen peroxide (H₂O₂), an AcOH/H₂O₂ mixture, dimethylformamide (DMF), and dimethyl sulfoxide (DMSO). Among these, DMSO achieved 92% resin removal in 9 min at 350 °C. Recycled fibres retained 1.48 ± 0.41 GPa strength (81% of virgin). Gas chromatography–mass spectrometry (GC–MS) analysis of pyrolysis oils revealed predominantly phenolic products with limited bisphenol A (BPA) retention. To demonstrate practical relevance, the semi-wet method was applied to real wind blade waste, where recovered fibres retained 72% of their tensile strength versus virgin fibres. These results indicate that the process remains effective for industrially aged GFRP. This study confirms the feasibility of MW-based semi-wet recycling and offers insights to support future process refinement, which will ultimately contribute to more sustainable end-of-life solutions for GFRP waste. Full article

Peroxymonosulfate (PMS)-based advanced oxidation is often hindered by pH instability and the lack of post-reaction separation. Herein, commercial magnesium hydroxide (Mg(OH)₂) is introduced as a multifunctional catalyst to address these limitations. Mg(OH)₂ effectively catalyzed PMS decomposition via a nonradical pathway dominated by singlet oxygen (¹O₂) generation, achieving rapid and complete degradation of electron-rich pollutants like bisphenol A (BPA) within 40 min. The system exhibits exceptional pH self-regulation, stabilizing the solution at ~9.8 and maintaining high efficiency across an initial pH range of 3–11. Mechanistic studies confirm ¹O₂ as the primary reactive species with a steady-state concentration of 1.67 × 10⁻¹² M. The catalyst demonstrates strong resistance to common anions and humic acid, along with excellent stability over four cycles. Furthermore, Mg(OH)₂ enables in situ flocculation and removal of degradation products. This work highlights Mg(OH)₂ as an efficient, stable, and multifunctional activator, offering a integrated strategy for practical wastewater treatment. Full article

Bisphenol A (BPA) is a persistent environmental contaminant requiring effective removal strategies. Biofilms offer advantages over conventional activated sludge for refractory compound degradation, yet the specific microorganisms and mechanisms driving BPA removal in biofilms remain poorly understood. This study employed an integrated approach, combining ¹³C-DNA stable isotope probing (SIP) and metagenomics to identify BPA-assimilating microorganisms and elucidate their metabolic pathways in biofilms. Two moving bed biofilm reactors (MBBRs) were operated at contrasting BPA concentrations (500 μg/L and 10 mg/L) to enrich distinct microbial communities. Using DNA-SIP, we revealed differences in assimilating bacteria across diverse concentrations of BPA-enriched biofilms. Simultaneously, we reconstructed the genomes of these assimilating bacteria, dissecting the functional genes essential to the degradation process and identifying significant gene variations among different assimilating bacteria. By integrating these gene functions, we constructed the BPA metabolic pathway, which surprisingly comprised genes from various assimilating bacteria. This research significantly advances our understanding of BPA-assimilating bacteria within biofilms and provides valuable insights for refining biofilm technologies aimed at BPA removal from wastewater. Full article

Designing and constructing heterojunctions has emerged as a pivotal strategy for improving the photocatalytic efficiency of semiconductors. In this study, we report the controlled synthesis of an Au/Zn₃In₂S₆ Schottky junction through a combination of hydrothermal and in situ photodeposition methods. The structural, morphological, and photoelectrochemical properties of the catalyst were meticulously characterized using a suite of techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), photoelectrochemical (PEC) measurements, and electron spin resonance (ESR) spectroscopy. The optimized 3% Au/Zn₃In₂S₆ composite exhibited a remarkable enhancement in both photocatalytic activity and stability, achieving a 90.4% removal of bisphenol A (BPA) under UV–visible light irradiation within 100 min. The corresponding first-order reaction rate constant was approximately 1.366 h⁻¹, nearly 4.37 times greater than that of the pristine Zn₃In₂S₆. This substantial improvement can be attributed to several key factors, including increased BPA adsorption, enhanced light absorption, and the efficient charge separation facilitated by the Au/Zn₃In₂S₆ heterojunction. Photogenerated holes, superoxide radicals, and hydroxyl radicals were identified as the primary reactive species responsible for the BPA degradation. This work highlights the potential of metal-modified semiconductors for advanced photocatalytic applications, offering insights into the design of highly efficient materials for environmental remediation. Full article

CuO/TiO₂ is a highly active visible-light-driven photocatalyst. The precise structural regulation of TiO₂ and the quantum dot-scale loading strategy of CuO have long been researching hotspots and challenges. This work presents an ingenious synthetic strategy, leveraging the photoinduced superhydrophilicity and dark-induced reversible hydrophobicity of TiO₂, coupled with carbon quantum dots (CQDs) as “seeds” to induce the in situ synthesis of CuO quantum dots (CuO QDs). Specifically, CuO QDs with an average diameter of 5–10 nm were successfully anchored onto TiO₂ nanowire arrays (TNWAs) with a diameter of 10–15 nm. By adjusting the dosage of “seeds” (CQDs), the loading amount of CuO QDs can be effectively controlled. Corresponding characterizations were performed, including ultraviolet-visible-near-infrared (UV-Vis-NIR spectroscopy) for optical absorption properties, photoluminescence (PL) spectroscopy for photoluminescent behavior, electron paramagnetic resonance (EPR) spectroscopy for free radical generation capability, and bisphenol A (BPA) degradation assays for photocatalytic performance. Loading 4.78 wt% CuO QDs can effectively inhibit the recombination of electron–hole pairs in TNWAs. Simultaneously, it prolongs the lifetime of charge carriers (photoelectrons) and enhances the yields of hydroxyl radicals (•OH) and superoxide radicals (•O₂⁻). The BPA degradation efficiency of the CuO QDs/TNWA composite is 2.4 times higher than that of TNWAs. Furthermore, we found that the loading of CuO QDs significantly modulates the depletion layer width of the P–N heterojunction, and the underlying mechanism has been discussed in detail. Full article

The degradation of bisphenol A (BPA), the main monomer of polycarbonate, was investigated under subcritical water conditions to better understand its decomposition as a function of process conditions and to provide useful data for designing a recycling process to convert polycarbonate into valuable products. Hydrothermal experiments were conducted in a batch reactor at temperatures ranging from 250 to 350 °C, with reaction times from 5 to 30 min and water-to-material ratios of 5, 10, and 15 (mL/g), following a Box–Behnken design with response surface methodology (RSM). The influence of process parameters on phase distribution, total carbon content, and product composition was evaluated. The results showed that temperature and reaction time were the most significant factors affecting BPA decomposition, while the water-to-material ratio had a minor effect. The recovery of the DEE (diethyl ether)-soluble phase decreased with increasing temperature and time, accompanied by a corresponding increase in the water-soluble phase yield and total carbon content. Analysis of the DEE-soluble fraction revealed the sequential transformation of BPA into 4-isopropenylphenol, 4-isopropylphenol, and phenol, with phenol becoming the dominant degradation product at higher temperatures. These findings provide new insights into the hydrothermal decomposition mechanism of BPA and form a basis for understanding polycarbonate degradation and developing sustainable subcritical water recycling processes for polymeric materials. Full article

Micro-nano bubbles (MNBs) have been widely used in water treatment due to their large specific surface area, long retention time, and high zeta potential. This study investigated the degradation of bisphenols by activating persulfate (PDS, an oxidizing agent) with air MNBs (MNBs/PDS). The removal rate of bisphenol A (BPA) in the MNBs/PDS process was 98.3% within 25 min, while there was almost no degradation observed by PDS or MNBs alone. This enhancement was attributed to the huge amount of energy released during the collapse of MNBs, sufficient to break the O–H bonds of water molecules or the O–O bond of PDS to induce the formation of reactive oxygen species (ROS, such as HO^• and SO₄^•−). To qualitatively analyze ROS generated in this system, electron paramagnetic resonance and quenching experiments were conducted, and the HO^• and SO₄^•− were detected in MNBs/PDS. Furthermore, the degradation percentages of bisphenols after 25 min of MNBs/PDS treatment followed the order of bisphenol B (100%) > BPA (98.3%) > bisphenol E (87.9%) > bisphenol F (86.5%) > bisphenol AF (84.9%) > bisphenol S (51%). Higher PDS dosage, higher gas flow rate, and lower pH values were preferred for the degradation. Moreover, the MNBs/PDS treatment reduced the TOC of secondary effluent containing BPA by 45.8% in one hour, indicating the application potential of MNBs/PDS in the advanced treatment of wastewater. Full article

It is generally found that enhancement in catalytic activity comes at the expense of selectivity or stability. In this study, an SO_x²⁻-modified Mn₂O₃ (SO-Mn₂O₃) solid catalyst was prepared using a simple oxalate precipitation method. This catalyst exhibited not only high catalytic activity but also high selectivity and good cycling stability. The degradation ratio of bisphenol A (BPA) under SO-Mn₂O₃ activated potassium peroxymonosulfate (PMS) achieved over 99% within 10 min, and the mineralization ratio increased to 83.2%. Particularly, the degradation rate for BPA under the SO-Mn₂O₃/PMS system was 15 times that of Mn₂O₃. Furthermore, the degradation ratio remained at 93.3% after five consecutive cycles. Multiple experimental characterizations confirmed that the introduction of SO_x²⁻ into Mn₂O₃ shifted the oxidative degradation pathway from a mixture of radical and non-radical routes to a predominantly non-radical pathway. This suppressed radical generation promoted the selective formation of high-valence metallic-oxo (Mn(V)=O) species and singlet oxygen (¹O₂), thereby significantly enhancing the catalytic activity. In addition, the SO-Mn₂O₃/PMS system exhibited broad applicability towards the degradation of other phenolic pollutants, strong anti-interference capability against complex water matrices, and suitability for efficient removal of organic contaminants in such environments. This research offers new perspectives for the design of selective catalysts for PMS activation. Full article

The widespread presence of bisphenol A (BPA), a persistent endocrine-disrupting pollutant, in aquatic environments poses significant ecological and health risks, necessitating its effective removal. However, conventional remediation technologies are often hampered by catalysts with narrow pH adaptability and poor stability. In this study, a novel catalyst, Zeolite-supported Cu₃Mn-layered double hydroxide (LDH), was fabricated using the co-precipitation method. The synthesized catalyst was applied to activate peroxymonosulfate (PMS), effectively enabling decomposition of BPA by advanced oxidation processes. The composite material was characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM), which confirmed the successful synthesis of the zeolite-supported Cu₃Mn-LDH. The catalyst exhibited high activity in both neutral and strongly alkaline environments, achieving complete degradation of 10 mg⋅L⁻¹ bisphenol A (BPA) within 40 min and a 98% total organic carbon (TOC) removal rate when both the PMS and catalyst were dosed at 0.15 g⋅L⁻¹. Singlet oxygen was detected as the primary reactive species responsible for BPA degradation, as verified by quenching experiments and EPR analysis, which also identified the presence of sulfate (SO₄^•−), hydroxyl (•OH), and superoxide (•O₂⁻) radicals. The catalyst exhibited excellent reusability, maintaining high catalytic efficiency over two consecutive cycles with minimal performance loss. Gas chromatography-mass spectrometry (GC-MS) analysis revealed five intermediate products, enabling the proposal of potential BPA degradation pathways. This work not only presents a novel synthetic approach for zeolite-supported LDH composites, but also offers a promising strategy for the efficient removal of BPA from aqueous systems through AOPs. Full article

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