Search Results (69)

In this study, the BPTCD/g-C₃N₄ heterojunction photocatalyst was successfully prepared by the hydrothermal method. BPTCD (3,3′,4,4′-benzophenone tetracarboxylic dianhydride) is immobilised on the surface of g-C₃N₄ by non-covalent π-π stacking. The BPTCD/g-C₃N₄ heterojunction photocatalyst is an all-organic photocatalyst with significantly improved photocatalytic performance compared with g-C₃N₄. BPTCD/g-C₃N₄-60% was able to effectively degrade MO solution (10 mg/L) to 99.9% and 82.8% in 60 min under full spectrum and visible light. The TOC measurement results indicate that MO can ultimately be decomposed into H₂O and CO₂ through photocatalytic action. The photodegradation of methyl orange by BPTCD/g-C₃N₄ composite materials under sunlight is mainly attributed to the successful construction of the heterojunction structure and its excellent π-π stacking effect. Superoxide radicals (^•O₂⁻) were found to be the main active species, while ^•OH and h⁺ played a secondary role. The synthesised BPTCD/g-C₃N₄ also showed excellent stability in the activity of photodegradation of MO in wastewater, with the performance remaining above 90% after three cycles. The mechanism of the photocatalytic removal of MO dyes was also investigated by the trap agent experiments. Additionally, BPTCD/g-C₃N₄-60% demonstrated exceptional photodegradation performance in the degradation of methylene blue (MB). BPTCD/g-C₃N₄ heterojunctions have great potential to degrade organic pollutants in wastewater under solar irradiation conditions. Full article

Asbestos cement materials represent a persistent source of environmental contamination, particularly in urban areas where weathering facilitates the release of hazardous chrysotile fibres. Despite extensive research on the human health impacts of asbestos, ecological interactions remain poorly understood. This paper explores the dual role of bryophytes colonising asbestos cement roofing as passive filters that trap airborne fibres and as vulnerable organisms subjected to asbestos-induced stress. Using a synthesis of recent findings, we assess the capacity of mosses to immobilise chrysotile fibres through their dense, mat-like structures, potentially reducing local dispersion. Simultaneously, we examine physiological and biochemical responses to prolonged fibre exposure, including reduced photosynthetic activity and signs of oxidative stress. The findings highlight a paradoxical function of bryophytes: while they contribute to pollution mitigation, they also accumulate contaminants and suffer from sublethal damage. These interactions may have broader implications for contaminant redistribution, particularly through decomposition and trophic transfer. Understanding these dynamics is essential for advancing ecological risk assessments and developing sustainable remediation strategies in asbestos-contaminated habitats. Full article

Adsorption represents an effective strategy for water remediation applications, particularly when utilising eco-friendly materials in a circular economy framework. This approach offers significant advantages, including low cost, material availability, ease of operation, and high efficiency. Herein, the performance of cadmium ion adsorption onto hydroxyapatites, derived through a calcination-free process from shells of two mollusc species, Queen Scallop (Aequipecten opercularis) and Pacific Oyster (Magallana gigas), is examined. The phase and morphology of the synthesised adsorbents were investigated. The results showed that hydroxyapatites obtained from mollusc shells are characterised by high efficiency regarding cadmium removal from water, exhibiting rapid kinetics with equilibrium achieved within 5 min and high adsorption capacities up to 334.9 mg g⁻¹, much higher than many waste-based adsorbents reported in literature. Structural investigation revealed the presence of Cadmium Hydrogen Phosphate Hydrate in the hydroxyapatite derived from oyster shells loaded with Cd, indicating the formation of a solid solution. This finding suggests that the material not only has the capability to decontaminate but also to immobilise and store Cd. Overall, the results indicate that hydroxyapatites prepared via a synthetic route in mild conditions from waste shells are an economical and efficient sorbent for heavy metals encountered in wastewater. Full article

Lithium–sulfur batteries (LSBs), with a high energy density (2600 $\mathrm{W}$$\mathrm{h}$ kg⁻¹) and theoretical specific capacity (1672 mA h g⁻¹), are considered the most promising next-generation rechargeable energy storage devices. However, polysulfide dissolution and the shuttle effect cause severe capacity fading and the rapid loss of the active material; hence, these must be addressed first. This review provides an overview of various strategies employed to immobilise polysulfides via polysulfide trapping and physical and chemical adsorption using porous cathode designs, heterostructures, functionalised separators, and polymer binders. The working mechanism of each strategy is reviewed and discussed, highlighting their advantages and disadvantages, and they are analysed through comparisons of the battery performance and limitations in terms of practical applications. Finally, the future prospects for the design and synthesis of LSBs to limit polysulfide dissolution are discussed. Full article

Diradical character is one of the characteristic quantities of functional open-shell molecules. Prof. Nakano devotedly studied the relationship between diradical character and material properties of open-shell molecules; now, we can use the diradical character as a powerful tool for molecular material designs. It is still unclear how the open-shell molecules are affected by the interaction with the surface although the molecules have been immobilised for device applications. In the present study, the adsorptions of model diradical molecules with s-electrons on the MgO (001) and BaO (001) surfaces are investigated using approximate spin projected density functional theory with plane-wave basis (AP-DFT/plane-wave) to provide a systematic discussion of surface–diradical interactions. The accuracy of AP-DFT/plane-wave was verified by comparisons with the calculated results by NEVPT2. The computational error introduced by DFT calculations on the diradical state (spin contamination error) is reduced by the surface–diradical interaction. In addition, it is shown that (1) the diradical character is amplified by the orbital polarisation effects of oxide ions, and (2) the character decreases when the magnetic orbitals become electron-rich due to electron donation from the surfaces. The two effects are competing; the former is pronounced in Au systems, whereas the latter is pronounced in Ag systems. Full article

Efflorescence, a time-dependent and water-driven phenomenon, is a major concern in alkali-activated materials (AAMs), impacting their practical use and preservation in a time-frozen state for post-characterisation. Although a method for stopping chemical reactions in conventional cements exists, it is time-consuming and not chemical-free. Therefore, this study explored the effects of low-power microwave-induced dehydration on efflorescence, mechanical performance, and structural integrity in AAMs, to create an alternative and more “user-friendly” dehydration method. For this purpose, several mixtures based on secondary raw (slag, fly ash, glass wool, and rock wool) and non-waste (metakaolin) materials were activated with a commercial Na-silicate solution in ratios that promoted or prevented efflorescence. Characterisation techniques, including Fourier-transform infrared spectroscopy and X-ray diffraction, showed that microwave dehydration effectively removed water without altering crystallinity, while mercury intrusion porosimetry and compressive strength tests confirmed increased porosity. In addition to being an efficient, time-saving, and solvent-free manner of stopping the reactions in AAMs, microwave irradiation emerged as an innovative, chemical-free method for evaluating curing finalisation and engineering foams in a stage when all other existing methods fail. However, the artificially provoked efflorescence in aged dehydrated AAMs connected the slipperiness of AAM with the instant extraction of Na, which raised the need for further research into alternative alkali replacements to evaluate the practical use of AAM. Full article

For the first time, N-modified analogues of VV-hemorphin-5 (Valorphin) were synthesised and conjugated with three different 4-substitured-1,8-naphthalimides (H-NVal without substituent, Cl-NVal with chloro-substituent, and NO₂-NVal with nitro-substituent). Cotton fabric was modified with these peptides by soaking it in their ethanol solution, and the colourimetric properties of the obtained fabric were measured. The fluorescent analysis shows that peptide immobilisation on a solid matrix as fabric decreases the molecule flexibility and spectrum maxima shift bathocromically with the appearance of a vibrational structure. The peptides’ contact antimicrobial activity, and the resulting fabrics, have been investigated against model Gram-positive B. cereus and Gram-negative P. aeruginos bacteria. For the first time, the influence of light on bacterial inactivation was investigated by antibacterial photodynamic therapy of similar peptides. Slightly more pronounced activity in liquid media and after deposition on the cotton fabric was obtained for the peptide containing 4-nitro-1,8-naphthalimide compared to the other two peptides. Immobilisation of a peptide on the surface of fibres reduces their antimicrobial activity since their mobility is essential for good contact with bacteria. Cotton fabrics can be used in medical practice to produce antibacterial dressings and materials. Full article

Diatomite, a natural adsorbent rich in active silica, serves as a valuable precursor for geopolymer synthesis. The safe disposal of diatomite as a failed lead (Pb(II)) adsorbent is critical to prevent secondary contamination. This study investigated the immobilisation efficiency of geopolymerisation for Pb(II)-rich diatomite sludge. Low-grade diatomite with high ignition loss was utilised in the synthesis of alkali-activated geopolymers. It was demonstrated that the geopolymers achieved a compressive strength of 28.3 MPa with a 50% replacement rate of metakaolin by diatomite sludge, which was not a compromise in strength compared to that of the geopolymer with no Pb(II) (26.2 MPa). The leaching behaviour of Pb(II) was evaluated using water and acetic acid, yielding concentrations below 3 mg/L and immobilisation efficiencies of 95% in both scenarios. Analytical techniques including Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) elucidated the mineral composition and chemical environment of the geopolymers. These analyses revealed that Pb(II) migrated from diatomite pores, potentially forming soluble hydroxides under sufficient hydroxide, which then participated in condensation with silicon and aluminium monomers, effectively immobilising Pb(II) within amorphous aluminosilicate gels. Furthermore, the formation of the amorphous gels within diatomite pores hindered Pb(II) leaching, encapsulating Pb(II) effectively. This study presents a novel approach to immobilising heavy metals within building materials, enhancing mineral resource utilisation efficiency while addressing environmental contamination concerns. Full article

This study investigates the environmental impacts caused by the scaling up of the photocatalytic purification of drinking water using ultraviolet light-emitting diode technology. The life cycle assessment methodology was utilised to estimate the environmental impacts of two different reactor setups commonly used in lab-scale studies: an immobilised and a suspended TiO₂ catalytic system. The functional unit adopted was the treatment of 1 L of water with an initial 7.8 mg/L concentration of natural organic matter, achieving a final 1 mg/L concentration. The use of a suspended photocatalyst was found to have an environmental footprint that was 87% lower than that of the immobilised one. From the sensitivity analysis, the environmental hotspots of the treatment process were the electricity usage and immobilised catalyst production. Therefore, alternative scenarios investigating the use of a renewable electricity mix and recyclable materials were explored to enhance the environmental performance of the photocatalytic treatment process. Using a renewable electricity mix, a decrease of 55% and 15% for the suspended and immobilised catalyst, respectively, was observed. Additionally, the process of recycling the glass used to support the immobilised catalyst achieved a maximum reduction of 22% in the environmental impact from the original scenario, with 100 glass reuses appearing to provide diminishing returns on the environmental impact savings. Full article

Reusing waste as raw materials to produce other materials can entail a decrease in production costs and in the abusive use of natural resources. Furthermore, it can even improve the properties of the end product or material. In this sense, a review of the most relevant literature published in recent decades shows that numerous solutions have been proposed or implemented, such as its use to produce construction materials, catalysts, pigments, pozzolana, refractory materials, glass-ceramic products, etc. Our research group has verified the viability of using different types of waste as secondary raw materials to obtain several types of ceramic, glassy and glassceramic materials, as well as frits. This article highlights several types of industrial waste that have both non-toxic (Li, Ca and Mn) and highly toxic (Cr VI) differentiating elements that can be used in sintering and vitrification industrial processes to immobilise them or render them inert. We studied the compositions and characterised the various materials obtained, conducting toxicity and leaching tests on waste/materials designed with high amounts of chromium. A suggestion for future lines of research has been proposed. Full article

Polymer-based membranes represent an irreplaceable group of materials that can be applied in a wide range of key industrial areas, from packaging to high-end technologies. Increased selectivity to transport properties or the possibility of controlling membrane permeability by external stimuli represents a key issue in current material research. In this work, we present an unconventional approach with the introduction of silver nanoparticles (AgNPs) into membrane pores, by immobilising them onto the surface of polyethyleneterephthalate (PET) foil with subsequent physical modification by means of laser and plasma radiation prior to membrane preparation. Our results showed that the surface characteristics of AgNP-decorated PET (surface morphology, AgNP content, and depth profile) affected the distribution and concentration of AgNPs in subsequent ion-track membranes. We believe that the presented approach affecting the redistribution of AgNPs in the polymer volume may open up new possibilities for the preparation of metal nanoparticle-filled polymeric membranes. The presence of AgNPs on the pore walls can facilitate the grafting of stimuli-responsive molecules onto these active sites and may contribute to the development of intelligent membranes with controllable transport properties. Full article

For over a century, enzyme immobilisation has been proven to be a superior strategy to improve catalytic activity and reusability and ensure easy separation, easy operation, and reduced cost. Enzyme immobilisation allows for an easier separation of the enzyme from the reaction mixture, thus simplifying downstream processing. This technology protects the enzyme from degradation or inactivation by harsh reaction conditions, making it more robust and suitable to be used in various applications. Recent strategies of immobilisation methods, such as adsorption, cross-linking, entrapment or encapsulation, and covalent bonding, were critically reviewed. These strategies have shown promising results in improving enzyme stability, activity, and reusability in various applications. A recent development in enzyme immobilisation in nanomaterials and agrowaste renewable carriers is underlined in the current review. Furthermore, the use of nanomaterials and agrowaste carriers in enzyme immobilisation has gained significant attention due to their unique properties, such as high surface area, high mass transfer, biocompatibility, and sustainability. These materials offer promising outcomes for developing more efficient and sustainable immobilised enzymes. This state-of-the-art strategy allows for better control over enzyme reactions and enhances their reusability, leading to more cost-effective and environmentally friendly processes. The use of renewable materials also helps to reduce waste generation and promote the utilisation of renewable resources, further contributing to the development of a circular economy. Full article

This study addresses the pressing environmental problem of the emissions of ecotoxic heavy metals from high-temperature waste combustion processes, including incineration and pyrolysis. Such emissions pose a serious threat to ecosystems and human health. This study investigated the behaviour of the heavy metals Cu, Ni, and Pb during the combustion of various waste materials such as plastic waste, pharmaceutical waste, and pesticide waste. To limit the release of heavy metals into the exhaust gas stream, various additives were used: divanadium pentoxide (V₂O₅), borax (Na₂B₄O₇), and their mixtures with calcium oxide (CaO). Additionally, this study examined the impact of the content of chlorine heteroatoms (Cl) in burned waste materials on the emission levels of Cu, Ni, and Pb. The findings shed light on the mobility of ecotoxic heavy metals in high-temperature waste incineration processes (1273, 1373 K) and offer insight into strategies to improve their immobilisation in grate residues. At a temperature of 1273 K, V₂O₅ with CaO reduced Pb emissions by ~65% for plastic waste and by ~40% for pesticide. Full article

This article discusses research on the low-temperature pyrolysis of waste floor and furniture joinery as an example of chemical recycling. Pyrolysis was carried out at 425 °C to obtain solid, liquid, and gaseous products. In line with the circular economy concept, the waste was transformed into economical and environmentally friendly raw materials suitable for application. Research results related to the chemical composition and properties of pyrolysis products are shown, with particular emphasis on the migration process of acidic impurities, i.e., sulphur and chlorine. In some processes, the presence of such substances can be a problem. Research has shown the high potential for sulphur and chlorine migration in pyrolysis products. It was shown that for woodwork, the most sulphur was discharged with the pyrolysis gas and the least was immobilised in the oil fraction. For vinyl panels, more than 50% of the sulphur was immobilised in the char. Chlorine was immobilised mainly in the char and pyrolysis gas. A high chlorine content of 12.55% was found in the vinyl panel. At the same time, a high chlorine content was also found in the pyrolysis products of these panels. This value is several times higher than in wood-based waste. Full article

The oxygen reduction reaction (ORR) is a key cathodic reaction in energy-converting systems, such as fuel cells (FCs). Thus, it is of utmost importance to develop cost-effective and efficient electrocatalysts (ECs) without noble metals to substitute the Pt-based ones. This study focuses on polyoxometalate (POM)-based ECs for ORR applications. A Wells–Dawson POM salt K₇ [P₂W₁₇(FeOH₂)O₆₁].·20H₂O was immobilised onto graphene flakes and multiwalled carbon nanotubes doped with nitrogen, denominated as P₂W₁₇Fe@GF_N8 and P₂W₁₇Fe@MWCNT_N8. The successful preparation of the composites was proved with various characterisation techniques, including FTIR, XPS and SEM. Both materials showed good ORR performance in an alkaline medium with similar potential onset values of ~0.84 V vs. RHE and diffusion-limiting current densities of −3.9 and −3.3 mA cm⁻² for P₂W₁₇Fe@MWCNT_N8 and P₂W₁₇Fe@GF_N8, respectively. Furthermore, both composites presented low Tafel slopes (48–58 mV dec⁻¹). Chronoamperometric tests revealed that the as-prepared nanocomposites rendered a significant improvement achieving between 90 and 94% of current retention in tolerance to methanol in comparison with Pt/C, and moderate to good long-term electrochemical stability with current retentions comprised between 68 and 88%. This work reinforces the use of POMs as important electroactive species for the preparation of alternative ORR electrocatalysts, exhibiting good activity, stability and selectivity towards the ORR in the presence of methanol. Full article