Search Results (76)

Low-melting bioabsorbable polymers, such as poly(caprolactone-co-lactide) (PCLA), hold significant promise for biomedical applications. However, achieving high-precision micro- and nanotopographical functionalization remains a formidable challenge due to the material’s susceptibility to thermal deformation during conventional thermal molding processes. In this study, functional microstructured PCLA coatings were engineered via low-temperature nanoimprint lithography utilizing a TiO₂–SiO₂ gas-permeable mold. These molds were synthesized via a sol–gel method utilizing titanium dioxide and silicon precursors. The gas-permeable nature of the mold facilitated the efficient evacuation of trapped air and volatiles during the imprinting process, enabling the high-fidelity replication of microstructures (1.3 μm height, 3 μm pitch) and nanostructured PCLA coatings featuring linewidths as narrow as 600 nm. The resultant microstructured PCLA coatings demonstrated modulated surface wettability, evidenced by an increase in water contact angles from 70.1° to 91.4°, and exhibited enhanced FD4 elution kinetics. These results confirm morphology-driven functionalities, specifically hydrophobicity and controlled release capabilities. Collectively, these findings underscore the efficacy of this microfabrication approach for polycaprolactone-based materials and highlight its potential to catalyze the development of high-value-added biomaterials for advanced medical and life science applications. This study establishes a foundational framework for the practical deployment of next-generation bioabsorbable materials and is anticipated to drive innovation in precision medical manufacturing. Full article

Poly(vinyl chloride) (PVC) undergoes thermal degradation during processing and operation, which necessitates the use of effective thermal stabilizers. The purpose of this work is to comprehensively evaluate the potential of new hierarchically structured titanium phosphates (TiP) with controlled morphology as thermal stabilizers of plasticized PVC, focusing on the effect of morphology and Ti/P ratio on their stabilizing efficiency. The thermal stability of the compositions was studied by thermogravimetric analysis (TGA) in both inert (Ar) and oxidizing (air) atmospheres. The effect of TiP concentration and its synergy with industrial stabilizers was analyzed. An assessment of the key degradation parameters is given: the temperature of degradation onset, the rate of decomposition, exothermic effects, and the carbon residue yield. In an inert environment, TiPMSI/TiPMSII microspheres demonstrated an optimal balance by increasing the temperature of degradation onset and the residual yield while suppressing the rate of decomposition. In an oxidizing environment, TiPR rods and TiPMSII microspheres provided maximum stability, enhancing resistance to degradation onset and reducing the degradation rate by 10–15%. Key factors of effectiveness include ordered morphology (spheres, rods); the Ti-deficient Ti/P ratio (~0.86), which enhances HCl binding; and crystallinity. The stabilization mechanism of titanium phosphates is attributed to their high affinity for hydrogen chloride (HCl), which catalyzes PVC chain scission, a catalyst for the destruction of the PVC chain. The unique microstructure of titanium phosphate provides a high specific surface area and, as a result, greater activity in the HCl neutralization reaction. The formation of a sol–phosphate framework creates a barrier to heat and oxygen. An additional contribution comes from the inhibition of oxidative processes and the possible interaction with unstable chlorallyl groups in PVC macromolecules. Thus, hierarchically structured titanium phosphates have shown high potential as multifunctional PVC thermostabilizers for modern polymer materials. Potential applications include the development of environmentally friendly PVC formulations with partial or complete replacement of toxic stabilizers, the optimization of thermal stabilization for products used in aggressive environments, and the use of hierarchical TiP structures in flame-resistant and halogen-free PVC-based compositions. Full article

Novel high-entropy perovskite oxide powders were synthesized using a sol-gel process. The B-site contained five cations: chromium, cobalt, iron, manganese, and nickel. The B-site cations were present on an equiatomic basis. The A-site cation was lanthanum, with calcium doping. The amount of A-site doping varied from 0 to 30 at%, yielding a composition of La_1−xCa_x(Co_0.2Cr_0.2Fe_0.2Mn_0.2Ni_0.2)O_3−δ. The resulting perovskite powders were pressurelessly sintered in air at 1400 °C for 2 h. Sintered densities were measured, and the grain structure was imaged via scanning electron microscopy to investigate the effect of doping. Samples were cut and polished, and their resistance was measured at varying temperatures in air to obtain the electrical conductivity and the mechanism that governs it. Plots of electrical conductivity as a function of composition and temperature indicate that the increased configurational entropy of the perovskite materials has a demonstrable effect. Full article

The Life Cycle Cost Assessment (LCCA) methodology is widely used to determine the optimal thickness of thermal insulation for walls and roofs. The results depend on several factors, such as the degree day calculations method, the ambient or sol–air temperature, base temperature variations, and the heat capacity of the thermal envelope elements. This study aims to analyze the impact of solar radiation on mass walls with different orientations in five cities in northern Chile, which have severe solar climates. The goal is to determine the optimal thickness of expanded polystyrene insulation using the LCCA method, considering solar radiation, a varying base temperature, and validating results by analyzing the energy demand for heating and cooling of a typical house. The findings show that excluding solar radiation in the LCCA methodology can lead to an underestimation of the optimal insulation thickness by 21–39% for walls in northern Chile. It was also found that using variable monthly threshold temperatures for heating and cooling based on the adaptive thermal comfort model results in a slight underestimation (1–3%) of the optimal thickness compared to a constant annual temperature. An energy simulation of a typical house in five cities in northern Chile showed that neglecting the effect of solar radiation when determining the thermal insulation thickness for the studied wall can lead to a minor increase in heating and cooling energy demand, ranging from approximately 1% to 9%. However, this study emphasizes the importance of applying optimal insulation thickness for cities with more continental climates like Santiago and Calama, where the heating demand is higher than cooling. Full article

Green hydrogen production from water electrolysis (WE) is one of the most promising technologies to realize a decarbonized future and efficiently utilize intermittent renewable energy. Among the various WE technologies, the emerging anion exchange membrane (AEMWE) technology shows the greatest potential for producing green hydrogen at a competitive price. To achieve this goal, simple methods for the large-scale synthesis of efficient and low-cost electrocatalysts are needed. This paper proposes a very simple and scalable process for the synthesis of nanostructured NiCo- and NiFe-based electrode materials for a zero-gap AEMWE full cell. For the preparation of the cell anode, oxides with different Ni molar fractions (0.50 or 0.85) are synthesized by the sol–gel method, followed by calcination in air at different temperatures (400 or 800 °C). To fabricate the cell cathode, the oxides are reduced in a H₂/Ar atmosphere. Electrochemical testing reveals that phase purity and average crystal size significantly influence cell performance. Highly pure and finely grained electrocatalysts yield higher current densities at lower overpotentials. The best performing membrane electrode assembly exhibits a current density of 1 A cm⁻² at 2.15 V during a steady-state 150 h long stability test with 1 M KOH recirculating through the cell, the lowest series resistance at any cell potential (1.8 or 2.0 V), and the highest current density at the cut-off voltage (2.2 V) both at the beginning (1 A cm⁻²) and end of tests (1.78 A cm⁻²). The presented results pave the way to obtain, via simple and scalable techniques, cost-effective catalysts for the production of green hydrogen aimed at a wider market penetration by AEMWE. Full article

La_1−xCa_x(Co_0.25Cr_0.25Fe_0.25Ni_0.25)O_3−δ perovskite powders were prepared via a sol-gel process. The A-site was doped with calcium, while four elements—cobalt, chromium, iron, and nickel—in equiatomic amounts made up the B-site. The configurational entropy was calculated to increase with the addition of calcium from medium to high entropy. The synthesized powders were heated to 1400 °C in air for 2 h to sinter them. The effect of doping on the resulting sintered materials was observed via density measurements and electron microscopy. The electrical conductivity was measured in air as a function of temperature to 900 °C. Conductivity versus composition indicates that an increase in entropy has a marked effect on electrical conductivity, leading to two distinct relationships with temperature. Full article

The present paper deals with the synthesis, characterization, and properties of sol-gel-derived TiO₂/TeO₂/Nb₂O₅ nanopowders. The gels were prepared using a combination of organic [Ti (IV) n-butoxide, Nb (V) ethoxide (C₁₀H₂₅NbO₅)] and inorganic [telluric acid (H₆TeO₆)] precursors. The aging of gels was performed in air for several days in order to enable further hydrolysis. The phase formation of the gels was investigated by XRD upon heating in the temperature range of 200–700 °C. It was established that the gels heat-treated up to 300 °C exhibited a predominantly amorphous phase in all binary and ternary compositions. The amount of amorphous phase gradually decreased with increasing temperature, and the first TiO₂ (anatase) crystals were detected at about 400–500 °C. The average crystallite size of TiO₂ (anatase) in the powdered samples heat-treated at 400 °C was about 10 nm. By DTA, it was established that the decomposition of organics is accompanied by strong weight loss occurring in the temperature range of 200–300 °C. The completeness of the hydrolysis-condensation reactions was verified by IR and UV–Vis analyses. The UV–Vis spectra of the as-prepared gels exhibited red shifting of the cut-off. Photoluminescence spectra exhibited a change in intensity with varying temperature and composition. The performed photocatalytic tests showed that all powders possess photocatalytic activity toward Malachite green organic dye. The obtained nanopowders exhibited good antibacterial properties against E. coli ATCC 25922. The obtained samples can be considered as prospective materials for use as environmental catalysts. Full article

Zinc oxide nanoparticles (ZnO NPs) with varying levels of nitrogen (N) doping were synthesized using a straightforward sol–gel approach. The morphology and microstructure of the N-doped ZnO NPs were examined through techniques such as SEM, XRD, photoluminescence, and Raman spectroscopy. The characterization revealed visible changes in the morphology and microstructure resulting from the incorporation of nitrogen into the ZnO lattice. These N-doped ZnO NPs were used in the fabrication of conductometric gas sensors designed to operate at room temperature (RT) for detecting low concentrations of NO₂ in the air, under LED UV-Vis irradiation (λ = 400 nm). The influence of nitrogen doping on sensor performance was systematically studied. The findings indicate that N-doping effectively enhances ZnO-based sensors’ ability to detect NO₂ at RT, achieving a notable response (S = R/R₀) of approximately 18 when exposed to 5 ppm of NO₂. These improvements in gas-sensing capabilities are attributed to the reduction in particle size and the narrowing of the optical band gap. Full article

The European Union regards gallium as a crucial element. Because of that, the retrieval of gallium ions from secondary sources through diverse methodologies is of the utmost significance in an actual economical context. The primary goal of this study was to explore the viability of MgFe₂O₄ spinel as an adsorbent material for Ga(III) ions recovery from aqueous solutions. A spinel adsorbent material was synthesised by using the sol–gel synthesis method. After preparation, the obtained spinel was subjected to a thermal treatment, which resulted in modifications of its crystalline structure and morphology, in concordance with the calcination temperatures. Specifically, two distinct temperatures of 260 and 650 °C were utilised in the process, which was conducted in air. The second objective was represented by the physicochemical characterisation of the newly prepared adsorbent material by using various analytical techniques, e.g., Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM) and magnetic measurements. The optimal conditions for Ga(III) adsorption were established (S:L ratio, solution pH, contact time, temperature, initial Ga(III) concentration). Simultaneously, the obtained experimental data were modelled to prove the fact that the pseudo-second-order model explained the studied kinetics process and established its mechanism. Intraparticle diffusion was also studied to highlight the rate-determined step during the Ga(III) adsorption process. The equilibrium of the process was also studied, establishing that the Sips isotherm fitted the experimental data best, with a correlation coefficient R²~1, indicating that the studied adsorption process was homogeneous, the maximum adsorption capacity of spinel being 24.7 mg Ga (III)/g MgFe₂O₄. Thermodynamic parameters, involving ΔG°, ΔH° and ΔS°, were also calculated; negative values of ΔG° indicated that the adsorption was spontaneous. ΔH° proved to be endothermic, and the calculated ΔS° values being positive confirmed the fact that the process was spontaneous. Full article

Perovskite materials are promising for thermochemical energy storage due to their ability to undergo redox cycling over a wide temperature range. Although BaCoO₃ exhibits excellent air cycling properties, its heat storage capacity in air remains suboptimal. This study introduces Na into the lattice structure to enhance oxygen vacancy formation and mobility. DFT+U simulations of the surface structure of Na-doped BaCoO_3−δ indicate that incorporating Na improves surface stability and facilitates the formation of surface oxygen vacancies. Na_xBa_1−xCoO_3−δ compounds were synthesized using a modified sol–gel method, and their properties were investigated. The experimental results demonstrate that Na doping significantly enhances the redox activity of the material. The heat storage capacity increased by above 50%, with the Na_0.0625Ba_0.9375CoO_3−δ solid solution achieving a heat storage density of up to 341.7 kJ/kg. XPS analysis reveals that Na doping increases the concentration of surface defect oxygen, leading to more active oxygen release sites at high temperatures. This enhancement in redox activity aligns with DFT predictions. During high-temperature cycling, the distribution of Na within the material becomes more uniform, and no performance degradation is observed after 300 cycles. Even after 450 cycles, Na_0.0625Ba_0.9375CoO_3−δ retains over 96% of its initial redox activity, significantly outperforming fresh BaCoO_3−δ. These findings elucidate the mechanism by which Na doping enhances the thermochemical heat storage performance of BaCoO_3−δ and provide new insights for the design of perovskite-based materials. Full article

The objective of this study was to evaluate the applicability of zeolite Y as a catalyst for producing bisphenol F (BPF) from phenol and formaldehyde. Catalyst extrudates were prepared by extrusion after adding pseudoboehmite sol (PS) and Ludox (Lu) as alumina and silica binders, respectively. The compressive strength of the catalyst extrudates increased with the addition of Ludox. However, the formaldehyde conversion decreased as more Ludox was used as a binder, resulting in a decrease in the yield of BPF. This decrease is attributed to the reduction in the total amount of acid sites caused by the addition of Ludox. In this study, the Y_PS5_Lu5 catalyst was selected as the most suitable for BPF synthesis. In the BPF synthesis over the Y_PS5_Lu5 catalyst in a catalyst basket reactor, the optimum reaction temperature was determined to be 110 °C. The effect of stirring speed on the yield of BPF was found to be negligible in the range of 200 rpm to 350 rpm. The spent catalyst was able to recover a specific surface area and reaction activity similar to those of a fresh catalyst through regeneration in an air atmosphere at 500 °C. When the Y_PS5_Lu5 extruded catalyst was used in a continuous reaction in a fixed-bed reactor, there was no noticeable deactivation of the catalyst at low space velocities of the reactants. However, when the space velocity was increased to 18.0 h⁻¹, catalyst deactivation was clearly observed. This suggests that periodic regeneration of the catalyst is inevitable in a continuous reaction using the Y_PS5_Lu5 extruded catalyst. Full article

High-performance hydrogen sulfide (H₂S) sensors are mandatory for many industrial applications. However, the development of H₂S sensors still remains a challenge for researchers. In this work, we report the study of a TiO₂-based conductometric sensor for H₂S monitoring at low concentrations. TiO₂ samples were first synthesized using the sol-gel route, annealed at different temperatures (400 and 600 °C), and thoroughly characterized to evaluate their morphological and microstructural properties. Scanning electronic microscopy, Raman scattering, X-ray diffraction, and FTIR spectroscopy have demonstrated the formation of clusters of pure anatase in the TiO₂ phase. Increasing the calcination temperature to 600 °C enhanced TiO₂ crystallinity and particle size (from 11 nm to 51 nm), accompanied by the transition to the rutile phase and a slight decrease in band gap (3.31 eV for 400 °C to 3.26 eV for 600 °C). Sensing tests demonstrate that TiO₂ annealed at 400 °C displays good performances (sensor response Ra/Rg of ~3.3 at 2.5 ppm and fast response/recovery of 8 and 23 s, respectively) for the detection of H₂S at low concentrations in air. Full article

Doping inorganic acid ions represents a promising pathway to improving the photocatalytic activity of TiO₂, and oxygen vacancy has been regarded as the determinant factor for photocatalytic activity. A series of samples doped with Cl⁻, NO₃⁻, and SO₄²⁻ was prepared via a simple sol–gel method. Two different oxygen vacancies in the crystal layer of NO₃⁻/TiO₂ and Cl⁻/TiO₂ were found, and those are [Ti³⁺]-V₀-[Ti³⁺] and [Ti³⁺]-Cl, respectively. The photocurrent of NO₃⁻/TiO₂ with [Ti³⁺]-V₀-[Ti³⁺] is significantly greater than that of Cl⁻/TiO₂ with [Ti³⁺]-Cl. The least oxygen vacancy is in the gel layer of SO₄²⁻/TiO₂, and the negligible photocurrent is due to difficulty in forming a stable sol. Furthermore, the process conditions for the application of TiO₂ were investigated in this work. The optimal process parameters are to adjust the solution to pH = 3 during sol–gel preparation, to adopt 550 °C as the calcination temperature, and to use an alkaline electrolyte, while the rest of the preparation conditions remain unchanged. This work reveals a new avenue for designing efficient photocatalysts for air pollutant degradation. Full article

The efficiency of household dehumidifiers is affected by air temperature and the temperature used for regeneration. A regeneration temperature that is too high can lead to increased energy use, heat build-up in the desiccant wheel, and lower dehumidification efficiency. In this study, we developed a LiCl@Al-Fum composite material and evaluated it through physical characterization and module testing. The results show that the LiCl@Al-Fum composite with a 20% mass fraction is particularly effective as a desiccant material. Additionally, a 15% volume concentration of neutral silica sol was identified as the optimal binder concentration. A comparative analysis of the effects of glass-fiber desiccant wheels (GF DWs), aluminum desiccant wheels (Al DWs), and commercial desiccant wheels (CM DWs) on household dehumidifier performance revealed that the Al DWs outperformed the CM DWs, showing a 13% improvement in the dehumidification rate and a 12.56% increase in the DCPP. An increase in the dehumidifier structure led to increases in the dehumidification rate by 11.8%, 11.9%, and 10% and in the DCPP by 11.6%, 12.1%, and 10%, respectively. Moreover, the modifications resulted in a 3.85 °C, 3.34 °C, and 3.8 °C decrease in the temperature. Full article

In warm climates with high levels of solar irradiation, solar shading plays a determinant role on buildings’ envelope performance, both during summer and winter conditions. In this research, an evaluation of the solar shading effect on sunny façades through IR thermography non-destructive testing was performed. Sunny and shaded areas revealed temperature differences of 7.4 °C in summer conditions and up to 1.2 °C in wintertime. Moreover, solar shading was shown to be beneficial not only for decreasing surface temperature in summertime but also for reducing convective air flow in wintertime. In addition, it was found that the prevalence of dense shadows, especially with non-reflective materials in louvres, is favorable. External Thermal Insulation Constructive Systems (ETICS) must be shadowed and the use of clear colors is recommended to reinforce homogeneity in the surface in wintertime and reduce solar absorptance in summertime. Under steady-state calculations, thermal losses can be reduced up to 30% at night in wintertime and up to 50–60% at daytime in summertime because of the shadowing. However, another important finding lied in the confirmation of the performance gap that arises between using air temperature, sol-air temperature and the actual surface temperature data, in such a way that the two former implied high levels of inaccuracy and overestimated the performance of the buildings compared to the actual behavior. Some of the main conclusions can be extrapolated to other circumstances. Full article