Search Results (89)

Heavy metal contamination in natural waters and soils poses a significant environmental challenge, necessitating efficient and sustainable water treatment solutions. This study presents the computational design of low-density polyethylene (LDPE) films functionalized with iron oxide (Fe₃O₄) nanoparticles (NPs) for enhanced water purification applications. Composite materials containing 5%, 10%, and 15% were synthesized and characterized in terms of adsorption efficiency, surface morphology, and reusability. Advanced molecular modeling using BIOVIA Pipeline was employed to investigate charge distribution, functional group behaviour, and atomic-scale interactions between polymer chains and metal ions. The computational results revealed structure–property relationships crucial for optimizing adsorption performance and understanding geochemically driven interaction mechanisms. The LDPE/Fe₃O₄ composites demonstrated significant removal efficiency of Cu²⁺ and Ni²⁺ ions, along with favourable mechanical properties and regeneration potential. These findings highlight the synergistic role of mineral–polymer interfaces in water remediation, presenting a scalable approach to designing multifunctional polymeric materials for environmental applications. This study contributes to the growing field of polymer-based adsorbents, reinforcing their value in sustainable water treatment technologies and environmental protection efforts. Full article

To address the issue of surface glazing that occurs during prolonged polishing with gel tools, this study employs a triethanolamine (TEA)-based polishing fluid system to enhance the self-sharpening capability of the gel polishing disc. The inhibitory mechanism of TEA concentration on disc glazing is systematically analyzed, along with its impact on the gel disc’s frictional wear behaviour. Furthermore, the synergistic effects of process parameters on both surface quality and material removal rate (MRR) of SiC are examined. The results demonstrate that TEA concentration is a critical factor in regulating polishing performance. At an optimal concentration of 4 wt%, an ideal balance between chemical chelation and mechanical wear is achieved, effectively preventing glazing while avoiding excessive tool wear, thereby ensuring sustained self-sharpening capability and process stability. Through orthogonal experiment optimization, the best parameter combination for SiC polishing is determined: 4 wt% TEA concentration, 98 N polishing pressure, and 90 rpm rotational speed. This configuration delivers both superior surface quality and desirable MRR. Experimental data confirm that TEA significantly enhances the self-sharpening performance of gel discs through its unique complex reaction. During the rough polishing stage, the MRR increases by 34.9% to 0.85 μm/h, while the surface roughness S_a is reduced by 51.3% to 6.29 nm. After subsequent CMP fine polishing, an ultra-smooth surface with a final roughness of 2.33 nm is achieved. Full article

Money Art is a growing contemporary practice where artists transform banknotes into unique visual works. While conceptually powerful, these artworks present significant conservation challenges due to their fragile substrates and complex material compositions. This study investigates the degradation behaviour of UniPosca acrylic markers applied on zero-euro banknotes, drawing on the techniques of artist RichardHTT, and explores bio-based protective strategies suitable for their preservation. Laboratory samples were prepared to replicate the original artwork and subjected to accelerated ageing. A multi-analytical approach was employed, including multispectral imaging, Fourier trasform infrared (FTIR) and Raman spectroscopy, and scanning electron microscopy (SEM-EDS) colorimetric analysis. Thickness and adhesion properties were assessed with contact micrometry and peel tests, while wettability was evaluated through static contact angle measurements. Four biopolymer coatings, chitosan and chitosan–nanocellulose films with varying CNC concentrations, were evaluated for their transparency, mechanical stability, and compatibility with the substrate. Results showed that painted areas, especially those with blue and black pigments, experienced marked degradation, while, after coating application, samples demonstrated improved chromatic stability, hydrophobicity, and adhesion. Importantly, all coatings were fully removable via enzymatic cleaning with α-amylase, confirming their reversibility. This research highlights the potential of chitosan-based biocomposites as conservation materials for non-traditional artworks and contributes to developing tailored, reversible strategies for contemporary art preservation. Full article

Gallium nitride (GaN), as the core material of third-generation semiconductors, has important applications in high-temperature, high-frequency, and high-power devices, but its polishing process faces many challenges. In this work, a multifield synergistic material removal model is established to study the material removal behaviour by ultrasonic magnetorheological chemical compound polishing (UMCP) of gallium nitride wafers, and the polishing processing under different polishing solution compositions and processing conditions is used to examine the effects of the ultrasonic, chemical, and mechanical effects on the material removal rate. The results show that mechanical removal dominates during UMCP, the chemical enhancement is slightly greater than the ultrasonic action, and the synergistic interaction between the range of factors promotes better removal of the GaN materials. The percentage of mechanical removal by abrasives is about 25% to 44.63%, the mechanical removal by magnetorheological effect polishing pads is about 14.66% to 23.94%, the removal due to chemical action is about 15.52% to 23.41%, the removal due to ultrasonic action is about 11.73% to 14.66%, and the percentage of interactive removal is 6.47% to 14.36%. The abrasive composition significantly enhances the mechanical removal effect, and a higher abrasive concentration correlates to a stronger mechanical removal effect. The concentration of hydrogen peroxide has a superior effect on the chemical reaction, and too high or too low a concentration of hydrogen peroxide weakens the chemical action effect. The results of the study can provide a basis for further research on the material removal mechanism of the GaN UMCP process. Full article

The increasing demand for high-performance materials has led to an increase in the use of carbon fibre-reinforced plastics (CFRPs) in recent decades, increasing the waste from end-of-life materials and off-cuts. The recycling of CFRPs, especially when thermosetting matrices are used, still remains an open challenge for academia and industry, with chemical, thermal and mechanical strategies being explored. Among them, mechanical methods have garnered growing interest since they do not require high specific energy consumption or expensive apparatus. However, from the literature it was observed that when using these methods, traces of old matrix remain on the fibre’s surface, compromising the fibre–matrix adhesion efficiency and limiting their use in recycled composites. On the other hand, solvothermal methods are known for their high matrix dissolution efficiency that in turn improves the fibre–matrix adhesion. Therefore, in this paper, end-of-life CFRPs from the aeronautic sector were machined using a milling-based mechanical recycling method, while to remove the residual matrix from the fibre surface, the recovered chips were chemically treated with a two-step treatment at low temperature. Then, two types of recycled composite laminates were manufactured using the compression moulding technique: the first using recycled fibres only from the mechanical recycled method, and the second one using recycled fibres deriving from both recycling methods. The feasibility of the process was analysed observing that the additional chemical treatment led to a mass loss of almost 24% in the recycled fibres. FTIR analysis revealed the complete matrix dissolution since no spectra of epoxy resin groups were detected. Finally, the flexural behaviour of the recycled composites was investigated, revealing an increase in the flexural strength and modulus of the second sample typology, respectively, of almost 42% and 76% thanks to the improved fibre–matrix adhesion as a consequence of the solvothermal treatment. Full article

This study aims to investigate the behaviour of thermoplastic composites reinforced with natural fibres. Composite materials were developed using reactive methyl methacrylate (MMA) resin, commercially known as Elium^® (Arkema, Colombes, France), with the incorporation of cellulose nanocrystals (CNCs), dispersed in the matrix at different concentrations. Natural fibres, such as flax, were chemically treated by immersion in an aqueous solution based on NaHCO₃, during different periods of exposure. After this treatment, flax fibres were washed with distilled water and dried. The degree of fibre surface tension was measured in terms of the contact angle. Then, cellulose nanocrystals were incorporated and mixed in the thermoplastic resin, and the samples were developed via the incorporation of intercalated layers of treated flax fibres. The composites were produced using compression moulding. After that, the samples were evaluated, regarding their mechanical performance and morphology. The research results show that flax fibres treated with 9 wt. % NaHCO₃ for 48 h had improved flexural strength as a result of removing impurities and exposing hydroxyl groups that react with Na⁺ ions present in NaHCO₃, which enhances its mechanical properties. The incorporation of 1% CNCs into thermoplastic resin significantly enhanced the fibre/matrix interface, resulting in a remarkable 38% increase in flexural strength. These findings demonstrate the effectiveness of using treated natural fibres and CNCs to improve composites’ performance. Full article

This paper presents a practice-oriented numerical modelling procedure to assess the loadbearing capacity of reinforced concrete (RC) columns under axial compression loading. A simplified procedure was incorporated to analyse the performance of RC columns with corroded stirrups, a prevalent deterioration phenomenon in corroded RC columns. The modelling framework incorporates material and geometric nonlinearities caused by material and buckling failure under axial compression, utilising the Arc-length algorithm with integrated geometric imperfections. Stirrup corrosion scenarios were incorporated by removing stirrups and modifying core concrete confinement properties, providing a practice-oriented approach to assess the loadbearing capacity of corroded columns. The study focused on square RC columns that are commonly used in low-rise buildings with nominal reinforcement detailing. The modelling method was validated against experimental data, and it showed a good agreement. A comprehensive parametric analysis was then conducted to examine the effects of critical design parameters, including (1) slenderness, (2) eccentricity, (3) stirrup corrosion, and (4) material properties, on axial compression performance. Parametric analyses demonstrated that the developed modelling technique appropriately predicted the axial compression behaviour of un-corroded RC columns in alignment with analytical design rules. For stirrup-corroded RC columns, the absence of confinement for up to 300 mm length near the base, due to stirrup corrosion, led to premature buckling. Based on the analysed cases, the reduction in bearing capacity of the stirrup-corroded RC columns could range between 4.9 and 18.6% (higher for slender columns) as compared to corresponding un-corroded RC columns. Full article

We used density functional theory with a hybrid functional to investigate the structure and properties of [4H]_Si (hydrogarnet) defects in α-quartz as well as the reactions of these defects with electron holes and extra hydrogen atoms and ions. The results demonstrate the depassivation mechanisms of hydrogen-passivated silicon vacancies in α-quartz, providing a detailed understanding of their stability, electronic properties, and behaviour in different charge states. While fully hydrogen passivated silicon vacancies are electrically inert, the partial removal of hydrogen atoms activates these defects as hole traps, altering the defect states and influencing the electronic properties of the material. Our calculations of the hydrogen migration mechanisms predict the low energy barriers for H⁺, H⁰, and H⁻, with the lowest barrier of 0.28 eV for neutral hydrogen migration between parallel c-channels and a similar barrier for H⁺ migration along the c-channels. The reactions of electron holes and hydrogen species with [4H]_Si defects lead to the breaking of O–H bonds and the formation of non-bridging oxygen hole centres (NBOHCs) within the Si vacancies. The calculated optical absorption energies of these centres are close to those attributed to individual NBOHCs in glass samples. These findings can be useful for understanding the role of [4H]_Si defects in bulk and nanocrystalline quartz as well as in SiO₂-based electronic devices. Full article

Currently, water is being polluted via various anthropogenic activities, resulting in wastewater contaminated with multiple pollutants, including heavy metals. Hexavalent chromium is a toxic heavy metal that poses significant health risks upon exposure. Biocomposites are materials that are partially composed of organic substances that enhance different properties of a composite. The aim of this study was to evaluate the kinetic, isothermal, and thermodynamic behaviour of a cellulose-based biocomposite with polylactic acid (PLA) for the removal of Cr (VI) from synthetic water. The results indicated that the Freundlich and Elovich models provided the best fit for the isothermal and kinetic data, with R² values of 0.671 and 0.973, respectively, suggesting that the adsorption process was chemical in nature and occurred on a heterogeneous, multilayer surface. Additionally, the thermodynamic analysis revealed that the adsorption process was exothermic, irreversible, and non-spontaneous. This study presents an innovative approach to the removal of metal ions using a cellulose–PLA biocomposite for wastewater treatment, offering kinetic, isothermal, and thermodynamic data applicable to the adsorption of other heavy metals. Full article

This work presents a novel hydrothermally aided sol-gel method for preparation of mesoporous silica nanoparticles (MSNs) with a narrow particle size distribution and varied pore sizes. The method was carried out in alkaline media in presence of polyethylene glycol (PEG) and cetyltrimethylammonium chloride (CTAC) as dual templates and permitted the synthesis of spherical mesoporous silica with a high surface area (1011.42 m²/g). The MSN materials were characterized by FTIR, Thermogravimetric (TG), Nitrogen adsorption and desorption and Field emission scanning electron microscopic analysis (FESEM). The materials feasibility as solid phase adsorbent has been demonstrated using cationic dyes; Rhodamine B (RB) and methylene blue (MB) as models. Due to the large surface area and variable pore width, the adsorption behaviors toward cationic dyes showed outstanding removal efficiency and a rapid sorption rate. The adsorption isotherms of RB and MB were well-fitted to the Langmuir and Freundlich models, while the kinetic behaviours adhered closely to the pseudo-second-order pattern. The maximum adsorption capacities were determined to be 256 mg/g for MB and 110.3 mg/g for RB. The findings suggest that MSNs hold significant potential as solid-phase nanosorbents for the extraction and purification of dye pollutants, particularly in the analysis and treatment of effluents containing cationic dyes. Full article

This study presents the synthesis, characterization, and evaluation of hybrid hydrogels based on calcium alginate (Ca-Alg) and synthetic nanoclay LaponiteRD (Lap), with an emphasis on their swelling and sorption properties. The motivation behind the development of these hybrid hydrogels stems from the need for sustainable materials with enhanced mechanical strength, swelling properties, and sorption capacity for environmental remediation and controlled-release applications. Synthesis methods for the ionotropically cross-linked Ca-Alg hydrogel and Alg–Lap composite hydrogels, based on Alg and Lap in the form of granules and fibres, have been developed. The Fourier-transform infrared spectroscopy (FTIR), Energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD) analyses of composite hydrogels confirmed the successful incorporation of Lap into the Ca-Alg matrix, indicating strong interactions between the polymer and clay, which enhanced the structural integrity of the hydrogels. The morphology of the surface and pore structure of nanocomposites were studied using Scanning Electron Microscopy (SEM). The swelling behaviour of the nanocomposites was largely dependent on the concentrations of Lap and the cross-linking agent (CaCl₂), with higher concentrations leading to more rigid, less swellable structures due to the increased cross-linking density. The sorption studies, specifically with Fe(II) ions, demonstrated that the hybrid hydrogels possess a large sorption capacity, with Lap contributing to selective sorption at lower Fe(II) ion concentrations and Alg enhancing overall capacity at higher concentrations. This suggests that the synergistic interaction between Alg and Lap not only improves mechanical stability but also tailors the sorption properties of the hydrogels. These findings position the Alg-Lap hydrogels as promising materials for a range of environmental applications, including wastewater treatment, heavy metal ion removal, and the design of advanced filtration systems. The study’s insights into the tunability of these hydrogels pave the way for further research into their use in diverse fields such as biomedicine, agriculture, and industrial water management. Full article

Blackcurrant pomace (BCP) is an example of an annual, high-volume, under-utilized renewable resource with potential to generate chemicals, materials and bioenergy within the context of a zero-waste biorefinery. Herein, the microwave-assisted isolation, characterization and potential application of defibrillated lignocelluloses from depectinated blackcurrant pomace are reported. Depectination was achieved using citric acid (0.2–0.8 M, 80 °C, 2 h, conventional heating) and compared with acid-free hydrothermal microwave-assisted processing (1500 W, 100–160 °C, 30 min). The resultant depectinated residues were subjected to microwave-assisted hydrothermal defibrillation to afford two classes of materials: namely, (i) hydrothermal acid-free microwave-assisted (1500 W, 160 °C, 30 min; DFC-M1-M4), and (ii) hydrothermal citric acid microwave-assisted (1500 W, 160 °C, 30 min; DFC-C1–C4). Thermogravimetric analysis (TGA) revealed that the thermal stability with respect to native BCP (T_d = 330 °C) was higher for DFC-M1-M4 (T_d = 345–348 °C) and lower for DFC-C1–C4 (322–325 °C). Both classes of material showed good propensity to hold water but failed to form stable hydrogels (5–7.5 wt% in water) unless they underwent bleaching which removed residual lignin and hemicellulosic matter, as evidenced by ¹³C solid-state NMR spectroscopy. The hydrogels made from bleached DFC-C1–C4 (7.5 wt%) and bleached DFC-M1-M4 (5 wt%) exhibited rheological viscoelastic, shear thinning, and time-dependent behaviour, which highlights the potential opportunity afforded by microwave-assisted defibrillation of BCP for food applications. Full article

This research is focused on the laboratory study of salt crystallization inhibitor products as new materials for conservation treatments which can be applied to mortars and painted plasters; as is well known, salt crystallization is one of the most frequent causes of decay processes on decorated architectural surfaces in a wide range of environments. Specifically, the study targets the field of the preventive conservation of mural paintings within rupestrian heritage sites. For the first time, systematic investigations were performed on mock-ups made of plaster painted with two different pigments: yellow ochre and carbon black. Two types of phosphonate inhibitors, PBTC (2-phosphonobutane-1,2,4-tricarboxylic acid) and ATMP (aminotris (methylene phosphonic acid)), were chosen and applied at two different concentrations. Given the limited literature available, and the presence of pigments potentially sensitive to treatment with salt inhibitors, preliminary tests were required. Their effects on the chromatic features of the pigments were evaluated visually and using colorimetry. The changes in the behaviour of water circulation in the mortar resulting from the treatments were evaluated through water vapour permeability and absorption tests. Accelerated crystallization experiments were carried out to assess how inhibitors could influence the growth of salts and the resulting material damage. The latter was carried out by employing sodium sulphate and calcium sulphate solutions, quantifying the damage to the specimens through material loss in weight and the percentage of painted surface loss. Based on the overall results, the product with the best performance was identified was ATMP 0.1% (by volume) in deionized water. The obtained results show that salt inhibitor treatments are promising for in situ application and could represent an innovative approach to promote the sustainable conservation of mural painting, particularly those located in hypogeal contexts, where the salt supply cannot be removed and slowing the growth of salts and/or changing their crystalline habitus may be effective in limiting their damage. Full article

Proton Exchange Membrane Fuel Cells (PEMFCs) represent a promising green solution for energy production, traditionally relying on platinum-group-metal (PGM) electrocatalysts. However, the increasing cost and limited global availability of PGMs have motivated extensive research into alternative catalyst materials. PGM-free oxygen reduction reaction (ORR) catalysts typically consist of first-row transition metal ions (Fe, Co) embedded in a nitrogen-doped carbon framework. Key factors affecting their efficacy include intrinsic activity and catalyst degradation. Thus, alternative materials with improved characteristics and the elucidation of reaction and degradation mechanisms have been the main concerns and most frequently explored research paths. High intrinsic activity and active site density can ensure efficient reaction rates, while durability towards corrosion, carbon oxidation, demetallation, and deactivation affects cell longevity. However, when moving to the actual application in PEMFCs, electrode engineering, which involves designing the catalyst layer, and other critical operational factors affecting fuel cell performance play a critical role. Electrode fabrication parameters such as ink formulation and deposition techniques are thoroughly discussed herein, explicating their impact on the electrode microstructure and formed electrochemical interface and subsequent performance. Adjusting catalyst loading, ionomer content, and porosity are part of the optimization. More specifically, porosity and hydrophobicity determine reactant transport and water removal. High catalyst loadings can enhance performance but result in thicker layers that hinder mass transport and water management. Moreover, the interaction between ionomer and catalyst affects proton conductivity and catalyst utilization. Strategies to improve the three-phase boundary through the proper ionomer amount and distribution influence catalyst utilization and water management. It is critical to find the right balance, which is influenced by the catalyst–ionomer ratio and affinity, the catalyst properties, and the layer fabrication. Overall, understanding how composition and fabrication parameters impact electrode properties and behaviour such as proton conductivity, mass transport, water management, and electrode–electrolyte interfaces is essential to maximize electrochemical performance. This review highlights the necessity for integrated approaches to unlock the full potential of PGM-free materials in PEMFC technology. Clear prospects for integrating PGM-free catalysts will drive cleaner and more cost-effective, sustainable, and commercially viable energy solutions. Full article

An important aspect of water treatment is removing fine-grain materials from water. Due to the properties of fine-grain materials, they are difficult to remove from water. During the sedimentation process, which takes place in settling tanks, such materials are removed. The sedimentation process is often accompanied by coagulation and flocculation processes, which form aggregates of particles (flocs) from the fine-grained material particles in a suspension (non-grainy suspension). This kind of suspension (consisting of aggregates of particles or flocs) shows a different behaviour when falling compared with classic grainy suspensions. The main goal and novelty of this article are to propose (and test) a modification of the often used Stokes’ formula with the addition of fractal geometry into the calculation of the terminal velocity of free-falling particles in order to overcome Stokes’ formula’s limitation, thus obtaining the sedimentation process efficiency. Because of this fractal modification, it is possible to use the simple and elegant Stokes’ formula in order to calculate better the terminal velocity of non-grainy particles—aggregates or flocs—and thus obtain the sedimentation efficiency for the whole range of suspensions, both non-grainy and grainy. The results obtained in this article show that the sedimentation process efficiency calculated by using the modified formula based on the fractal geometry morphology of particles (the proposed fractal method) describes and agrees more with the data from the experiment than the sedimentation efficiency calculated only based on particle size (classic method). Full article