Search Results (11,777)

Accelerating urbanisation and industrial activity have led to the widespread release of polycyclic aromatic hydrocarbons (PAHs), a class of persistent organic pollutants with serious ecological and health consequences. While physical and chemical remediation techniques are widely used, they often require nonrenewable resources and generate secondary waste. Fungal-based bioremediation offers a promising alternative, leveraging the unique metabolic pathways and structural properties of fungi to break down or adsorb PAHs. This review focuses on three strategies of PAH remediation in aquatic environments: biofiltration, biosorption, and metabolic degradation. We conduct a comparison between conventional systems and fungal approaches with reference to the literature (2000–2025). Fungal matrices are identified as being able to capture and adsorb PAHs, facilitating localised remediation that capitalises on the biological capabilities of fungal organisms while requiring lower resource inputs than conventional methods. This review highlights fungal matrices as multifunctional water filtration membranes and provides insights for the application and development of engineered living materials (ELMs) for the water detoxification of PAHs. Full article

Dye-contaminated wastewater has become one of the most severe environmental challenges due to the non-biodegradability and toxicity of synthetic dyes. While photocatalytic degradation is considered a green and efficient technology for wastewater purification, conventional TiO₂ suffers from limited light utilization and rapid electron–hole recombination. In this exploration, Ag-TiO₂-RGO nanocomposites were successfully fabricated and systematically investigated by XRD, SEM, TEM, XPS, Raman, and PL spectroscopy. The incorporation of Ag nanoparticles and reduced graphene oxide (RGO) synergistically improved charge separation and transfer efficiency. Photocatalytic activity was evaluated using different dyes as pollutants under visible light irradiation. Among the samples, Ag-TiO₂-RGO-3% exhibited the highest RhB degradation efficiency of 99.5% within 75 min, with a rate constant (K) of 0.05420 min⁻¹, which was nearly three times higher than that of pure TiO₂. The photocatalyst also showed excellent reusability with only minor efficiency loss after five cycles, and its activity remained stable across a wide pH range. Radical trapping experiments revealed that •O₂⁻ served as the dominant reactive species, with additional contributions from •OH and photogenerated holes (h⁺). A possible photocatalytic mechanism was proposed, in which Ag nanoparticles and RGO effectively suppressed electron–hole recombination and accelerated the formation of reactive oxygen species for efficient dye mineralization. These findings demonstrate that Ag-TiO₂-RGO-3% is a promising photocatalyst with high activity, stability, and environmental adaptability for wastewater remediation. Full article

P(3HB) is a biodegradable and biocompatible polymer, which can replace petroleum-derived plastics. Previous studies have shown that Azotobacter vinelandii strain OP-PhbP3⁺, which overexpresses the phasin protein PhbP3, produces high concentrations of P(3HB) and undergoes early autolysis, facilitating polymer release. The aim of the present study was to evaluate the performance of this strain for P(3HB) production in 3 L bioreactors and assess the feasibility of a simplified recovery process. After 36 h of cultivation, rapid cell lysis was observed, resulting in a ~50% decrease in the protein content of the cell dry weight, without reducing P(3HB) concentration, which reached 4.6 g L⁻¹. Flow cytometry analysis revealed significant morphological changes during cultivation, which was consistent with the strain’s lytic behavior. The biomass recovered at 36 h was washed with SDS, obtaining a yield of 92.5% (respect to P(3HB) initial) and a purity of 97.6%. An alternative extraction procedure using the non-halogenated solvent cyclohexanone (CYC) resulted in an even higher yield of 97.8% with a purity of 99.3% of P(3HB). Notably, the weight average molecular weight of the polymer remained stable at 8000 kDa during the entire process. Overall, the combination of PhbP3 over-expression and environmentally friendly solvents, such as CYC, enabled efficient P(3HB) production with high yield and purity while preserving polymer quality. Full article

Postoperative adhesion remains a major clinical challenge, often leading to chronic pain, functional disorders, and recurrent surgeries. Herein, we developed a multifunctional gelatin–polyphenol hydrogel (GPP20) featuring rapid gelation (within 5 min), strong tissue adhesion (lasting > 24 h under physiological conditions), and intrinsic wound healing capacity to achieve integrated prevention of postoperative adhesion. GPP20 was fabricated via dynamic crosslinking between gelatin and tea polyphenol, endowing it with injectability, self-healing, biodegradability, and excellent mechanical properties (shear stress of 14.2 N). In vitro studies demonstrated that GPP20 exhibited effective ROS scavenging (82% ABTS scavenging capability), which protects cells against oxidative stress, while possessing excellent hemocompatibility and in vivo safety. Notably, GPP20 significantly reduced postoperative cecum–abdominal wall adhesions through both physical barrier effects and modulation of inflammation and collagen deposition, demonstrating a comprehensive integrated prevention strategy. Furthermore, in full-thickness wound models, GPP20 accelerated tissue regeneration (85% wound closure rate on day 10) by promoting macrophage polarization toward the M2 phenotype and stimulating angiogenesis, thereby enhancing collagen deposition and re-epithelialization. Collectively, these findings demonstrate that GPP20 integrates anti-adhesion efficacy with regenerative support, offering a facile and clinically translatable strategy for postoperative care and wound healing. Full article

Titanium and its alloys are the most widely used metallic materials for bone contact implants. However, despite advances in implant technology, these alloys are still susceptible to post-operative clinical complications such as inflammation, which is often joined by infections and biofilm formation. A number of coatings were studied to overcome the drawbacks of these complications, but the controlled release of bioactive molecules over the first few days and the adhesion of the coating to the substrate remain recognized challenges. Carbon dots and the antibacterial potential of chiral carbon dots (CCDs) were recently reported, and their chirality was identified as a major contribution to the bactericidal effect. This study aimed to achieve a stimuli-responsive medium-term controlled release for up to one month. Two types of chiral carbon dots (CCDs) with distinct functional groups were incorporated into a stable and adherent biodegradable polymer coating, i.e., poly(lactic-co-glycolic acid) (PLGA). To enhance the coating adhesion, the titanium alloy surfaces were pre-treated and activated. The wettability, morphology, and surface composition of the coatings were characterized by contact angle, profilometry, SEM, and XPS, respectively. Coating degradation, adhesion, and CCDs release were studied at physiological pH (7.4) and at an acidic pH characteristic of an inflammatory site (pH 3.0) for up to one month. Their biological performances and blood compatibility were assessed as well. Degradation studies conducted over 28 days revealed a slow mass loss of approximately 10%, with maximum release rates for CCDs-OH and CCDs-NH₂ of 67% and 45% at pH 7.4, respectively. At pH 3.0 an inverse trend was observed with 49% and 59% maximum release after 28 days. Furthermore, the coatings did not exhibit any cytotoxic and hemolytic effects. These findings demonstrate the potential of this approach to providing titanium implants with pH-sensitive controlled release of bioactive CCDs lasting up to one month, which could address key challenges in implant-associated complications. Full article

Plastic remains a cheap material for numerous uses in households, industries, and engineering; however, it disintegrates in aquatic ecosystems to form smaller particles termed microplastics. Microplastics (MPs) have become a cause for concern due to their persistence and potential effects on freshwater ecosystems. Moreover, the toxicity of microplastics can be achieved through different mechanisms, including physical blockage and additive leaching, or they can function as vectors for other chemical pollutants. Microplastics were found to provide a growing surface for microbial communities, forming a biofilm termed the plastisphere. Microplastic pollution seems to need urgent attention globally; however, the comparability of results becomes a challenge due to the different techniques employed by different researchers. Moreover, the complete removal of MPs has proven to be an impossible task. This review explored MP occurrence in freshwater ecosystems, the role of microbial communities in the dynamics of microplastics, removal techniques, strategies for reduction in the environment, and their effect on freshwater ecosystems. Moreover, techniques to reduce microplastic release, such as recycling, plastic–fuel conversion, and biodegradable plastics, are explored. The review provides recommendations for reducing microplastic release and removal in freshwater ecosystems. This review stresses existing gaps to explore going forward in addressing microplastic pollution and possible removal techniques. Full article

With the continuous progress and innovation of petroleum engineering technology, the development of new oilfield additives with superior environmental benefits has attracted widespread attention. Konjac glucomannan (KGM) is a natural resource characterized by abundant availability, low cost, biodegradability, and environmental compatibility. Konjac gum easily forms a weak gel network in water, but its water solubility and thermal stability are poor, and it is easily degraded at high temperatures. Therefore, its application in drilling fluid and fracturing fluid is limited. In this paper, a method of carboxymethyl modification of KGM was developed, and a carboxymethyl group was introduced to adjust KGM’s hydrogel forming ability and stability. Carboxymethylated Konjac glucomannan (CMKG) is a water-soluble anionic polysaccharide derived from natural Konjac glucomannan. By introducing carboxymethyl groups, CMKG overcomes the limitations of the native polymer, such as poor solubility and instability, while retaining its safe and biocompatible nature, making it an effective natural polymer additive for oilfield applications. The results show that when used as a drilling fluid additive, CMKG can form a stable three-dimensional gel network through molecular chain cross-linking, significantly improving the rheological properties of the mud. Its unique gel structure can enhance the encapsulation of clay particles and inhibit clay hydration expansion. When used as a fracturing fluid thickener, the viscosity of the gel system formed by CMKG at 0.6% (w/v) is superior to that of the weak gel system of KGM. The heat resistance/shear resistance tests confirm that the gel structure remains intact under high-temperature and high-shear conditions, meeting the sand-carrying capacity requirements for fracturing operations. The gel-breaking experiment shows that the system can achieve controlled degradation within 300 min, in line with on-site gel-breaking specifications. This modification process not only improves the rheological properties and water solubility of the CMKG gel but also optimizes the gel stability and controlled degradation through molecular structure adjustment. Full article

The rapid growth of the human population and industrialization has intensified anthropogenic activities, leading to the release of various toxic chemicals into the environment, triggering significant risks to human health and ecosystem stability. One sustainable solution to remove toxic chemicals from various environmental matrices, such as water, air, and soil, is bioremediation, an approach utilizing biological agents. Microalgae, as the primary producers of the aquatic environment, offer a versatile bioremediation platform, where their metabolic processes break down and convert pollutants into less harmful substances, thereby mitigating the negative ecological impact. Besides the CO₂ sequestration potential, microalgae are a source of renewable energy and numerous high-value biomolecules. Additionally, microalgae can mitigate various toxic chemicals through biosorption, bioaccumulation, and biodegradation. These remediation strategies propose a sustainable and eco-friendly approach to address environmental pollution. This review evaluates the microalgal mitigation of major environmental contaminants—heavy metals, pharmaceuticals and personal care products (PPCPs), persistent organic pollutants (POPs), flue gases, microplastics, and nanoplastics—linking specific microalgae removal mechanisms to pollutant-induced cellular responses. Each section explicitly addresses the effects of these pollutants on microalgae, microalgal bioremediation potential, bioaccumulation process, the risks of trophic transfer, and biomagnification in the food web. Herein, we highlight the current status of the microalgae-based bioremediation prospects, pollutant-induced microalgal toxicity, bioaccumulation, and consequential biomagnification. The novelty of this review lies in integrating biomagnification risks with the bioremediation potential of microalgae, providing a comprehensive perspective not yet addressed in the existing literature. Finally, we identify major research gaps and outline prospective strategies to optimize microalgal bioremediation while minimizing the unintended trophic transfer risks. Full article

The rapid development of nanotechnology has significantly transformed the design and performance of glucose biosensors, leading to enhanced sensitivity, selectivity, and real-time monitoring capabilities. This review highlights recent advances in glucose-sensing platforms facilitated by nanomaterials, including metal and metal oxide nanoparticles, carbon-based nanostructures, two-dimensional materials, and metal–organic frameworks (MOFs). The integration of these nanoscale materials into electrochemical, optical, and wearable biosensors has addressed longstanding challenges associated with enzyme stability, detection limits, and invasiveness. Special emphasis is placed on non-enzymatic glucose sensors, flexible and wearable devices, and hybrid nanocomposite systems. The multifunctional properties of nanomaterials, such as large surface area, excellent conductivity, and biocompatibility, have enabled the development of next-generation sensors for clinical, point-of-care, and personal healthcare applications. The review also discusses emerging trends such as biodegradable nanosensors, AI-integrated platforms, and smart textiles, which are poised to drive the future of glucose monitoring toward more sustainable and personalized healthcare solutions. Full article

Biodegradable plastics are not a primary solution to plastic pollution, and empirical evidence on whether they are environmentally friendly remains lacking. In this study, we systematically compared the toxic effects of traditional microplastics (polypropylene, PP; polystyrene, PS) with biodegradable microplastics (polylactic acid, PLA; polyhydroxyalkanoates, PHA) on the haplic phaeozem ecosystem. Through mathematical modeling analysis, it was found that earthworms initially rely on antioxidant enzymes to resist stress, mid-term activation of detoxifying enzymes to repair damage, and maintaining physiological balance through metabolic regulation and immune enhancement in later stages. We elucidated their mechanism differences: PLA and PP caused severe damage to the antioxidant system and cell membrane, with PLA mainly relying on POD to clear peroxides and PP relying on GST. In addition, PLA and PS can induce early neurotoxicity (AChE), while PHA induces late neurotoxicity. Furthermore, this study provides direct evidence proving that biodegradable microplastics are not environmentally friendly by breaking through the one-way research framework of “microplastic biotoxicity” and innovatively constructing a path analysis model that links biological physiological responses with soil ecological functions. We also provide a scientific basis to evaluate the ecological risks of microplastic pollution in soil and the whether biodegradable plastics are truly environmentally friendly. Full article

Natural laccase is an environmentally friendly biocatalyst in the degradation of a broad range of toxic pollutants because its catalysis reaction does not require or produce toxic reactants and byproducts. However, its inherent limitations, such as operational sensitivity, poor stability, and difficulty in recovery/reusability, have significantly restricted its practical environmental applications. Consequently, in recent years, researchers have focused on the development of sustainable catalysts to mimic natural laccase. This review focuses on biomolecule-based laccase mimics, which are derived from nucleotides, nucleic acids, amino acids, peptides, and proteins, summarizing their environmental applications. These biomolecule-based laccase mimics not only overcome the limitations of natural laccase by offering advantages such as high stability, ease of recycling, and long-term storage but also exhibit excellent biodegradability, making them green and sustainable catalytic materials. This study aims to present recent progress in biomolecule-based laccase mimics, as well as their challenges, and to offer future directions in laccase-like catalysts for environmental applications. Full article

The Textiles and Clothing sector is increasingly focused on transitioning towards circular production, with industrial companies striving to integrate sustainable practices. Achieving this goal can involve the rapid adoption of innovative raw fibers (e.g., biodegradable and biobased materials) and maximizing the use of recycled and recyclable fibers. This implicitly demands acting on the total transparency of information along the complex supply chains in this sector to guarantee the correct adoption of these innovative fibers. It is precisely this complexity that hinders efforts to track and accurately disclose material usage. To address this issue, this paper presents a systematic literature review to explore the main challenges in adopting technologies like digital product passports, which can help track materials information along supply chains to support sustainable transitions. The analyzed articles were selected by excluding student thesis works, non-retrievable articles, papers that had a different focus, and literature published before 2020 or in non-institutional journals. The 53 resulting contributions are analyzed through a thematic analysis and discussed, focusing on identifying key material-related data that should be monitored to ensure responsible material use and strengthen sustainable production practices in the Textiles and Clothing sector, thereby guaranteeing control over material use and preventing premature disposal. Full article

The potential of elastomeric composites reinforced with natural fillers to replace traditional synthetic materials in applications involving exposure to acidic environments offers both economic and environmental advantages. On the one hand, these materials contribute to cost reduction and the valorization of organic waste through the development of value-added products. On the other hand, the presence of wood waste in the composite structure enhances biodegradation potential, making these materials less polluting and more consistent with the principles of the circular economy. The present study aims to evaluate the behavior of composites based on Ethylene Propylene Diene Monomer (EPDM) synthetic rubber, reinforced with silica and wood sawdust, in a weakly acidic yet strongly corrosive environment—specifically, acetic acid solutions with concentrations ranging from 10% to 30%. The study also investigates the extent to which varying the proportions of the two fillers affects the resistance of these materials under such environmental conditions. Physico-chemical, structural, and morphological analyses revealed that the materials underwent chemical modifications, such as acetylation of hydroxyl groups. This process reduced the hydrophilic character of the sawdust and, combined with the formation of stable interfaces between the elastomeric matrix and the fillers during vulcanization, limited acid penetration into the composite structure. The composites in which 20 phr or 30 phr of wood sawdust were used-replacing equivalent amounts of silica from the initial 50 phr formulation-demonstrated the highest resistance to the corrosive environments. After 14 days of exposure to a 20% acetic acid solution, the composite containing 30% wood sawdust exhibited a decrease in cross-link density of only 1.44%, accompanied by a reduction in Young’s modulus of just 0.95%. At the same time, tensile strength and specific elongation increased by 22.57% and 26.02%, respectively. FTIR and SEM analysis confirmed good rubber–filler interactions and the stability of the composite structure under acidic conditions. Full article

Biodegradable polymers offer a promising solution to the growing issue of global microplastic pollution. To effectively replace conventional plastics, it is essential to develop strategies for tuning the properties of biodegradable polymers without relying on additives. Biaxial stretching promotes anisotropic crystallization in polymer domains, thereby altering the mechanical performance of polymer blends. In this study, we employed a design of experiment (DoE) approach to investigate the effects of biaxial stretching at three drawing temperatures (T_ds) and draw ratios (λs) on a biodegradable blend of poly(lactic acid) (PLA) and poly(butylene adipate-co-terephthalate) (PBAT), aiming to optimize both the strength and ductility. The DoE analysis revealed that the composition, the λ, the interaction between the λ and composition, and the interaction between the T_d and composition significantly affect the elongation at break (ε_Break). For the stress at break (σ_Break), the most influential factors were the interaction between the λ and PLA concentration; a three-way interaction among the λ, PLA, and T_d; the T_d; the λ; and finally the PLA concentration alone. The optimal ε_Break and σ_Break were achieved at a λ = 5 × 5 and T_d = 110 °C, with a composition of 10% PLA and 90% PBAT. The stretched samples exhibited higher crystallinity compared to the pressed samples across all compositions. This work demonstrates that in addition to the composition, the processing parameters, such as the λ and T_d, critically influence the mechanical properties, enabling performance enhancements without the need for compatibilizers or toxic additives. Full article

Polyvinyl alcohol (PVA), a water-soluble, biodegradable, and biocompatible polymer, has garnered significant attention in recent years for its applications such as packaging, electronics, biomedical materials, and water treatment. However, its high flammability poses a substantial limitation in fire-sensitive environments. To address this challenge, significant research efforts have been devoted to improving the flame retardancy and suppressing the smoke toxicity of PVA through various strategies. This review presents diverse modification strategies that have been developed for PVA, including physical blending with polymers and nanofillers, chemical modifications such as esterification, acetalization, and crosslinking, and advanced surface engineering techniques such as plasma treatment, layer-by-layer assembly, and surface grafting. Beyond fire safety, these modifications enable multifunctional applications, expanding PVA use in optical, energy, sensing, and biomedical fields. Finally, this review explores current challenges, environmental considerations, and future directions for the development of sustainable, high-performance flame-retardant PVA systems. Full article