Search Results (100)

The demand for anion exchange membranes (AEMs) is growing due to their applications in water electrolysis, CO₂ reduction conversion and fuel cells, as well as water treatment, driven by the increasing energy demand and the need for a sustainable future. However, current AEMs still face challenges, such as insufficient permeability and stability in strongly acidic or alkaline media, which limit their durability and the sustainability of membrane fabrication. In this study, polyvinyl alcohol (PVA) and chitosan (CS) biopolymers are selected for membrane preparation. Zinc oxide (ZnO) and porous organic polymer (POP) nanoparticles are also introduced within the PVA-CS polymer blends to make mixed-matrix membranes (MMMs) with increased OH⁻ transport sites. The membranes are characterized based on typical properties for AEM applications, such as thickness, water uptake, KOH uptake, Cl⁻ and OH⁻ permeability and ion exchange capacity (IEC). The OH⁻ transport of the PVA-CS blend is increased by at least 94.2% compared with commercial membranes. The incorporation of non-porous ZnO and porous POP nanoparticles into the polymer blend does not compromise the OH⁻ transport properties. On the contrary, ZnO nanoparticles enhance the membrane’s water retention capacity, provide basic surface sites that facilitate hydroxide ion conduction and reinforce the mechanical and thermal stability. In parallel, POPs introduce a highly porous architecture that increases the internal surface area and promotes the formation of continuous hydrated pathways, essential to efficient OH⁻ mobility. Furthermore, the presence of POPs also contributes to reinforcing the mechanical integrity of the membrane. Thus, PVA-CS bio-based membranes are a promising alternative to conventional ion exchange membranes for various applications. Full article

Pyrochlore Bi_1.8Mn_0.5Ni_0.5Ta₂O_9-Δ (sp.gr. Fd-3m, a = 10.5038(9) Å) was synthesized by the solid-phase reaction method and characterized by vibrational and X-ray spectroscopy. According to scanning electron microscopy, the ceramics are characterized by a porous microstructure formed by randomly oriented oblong grains. The average crystallite size determined by X-ray diffraction is 65 nm. The charge state of transition element cations in the pyrochlore was analyzed by soft X-ray spectroscopy using synchrotron radiation. For mixed pyrochlore, a characteristic shift of Bi4f and Ta4f and Ta5p spectra to the region of lower energies by 0.25 and 0.90 eV is observed compared to the binding energy in Bi₂O₃ and Ta₂O₅ oxides. XPS Mn2p spectrum of pyrochlore has an intermediate energy position compared to the binding energy in MnO and Mn₂O₃, which indicates a mixed charge state of manganese (II, III) cations. Judging by the nature of the Ni2p spectrum of the complex oxide, nickel ions are in the charge state of +(2+ζ). The relative permittivity of the sample in a wide temperature (up to 350 °C) and frequency range (25–10⁶ Hz) does not depend on the frequency and exhibits a constant low value of 25. The minimum value of 4 × 10⁻³ dielectric loss tangent is exhibited by the sample at a frequency of 10⁶ Hz. The activation energy of conductivity is 0.7 eV. The electrical behavior of the sample is modeled by an equivalent circuit containing a Warburg diffusion element. Full article

Electrochemical formation of ceria (mixed Ce₂O₃ and CeO₂) coatings on different types of screen-printed carbon electrodes (SPCEs) (based on graphite (C110), carbon nanotubes (CNT), single-walled carbon nanotubes (SWCNT), carbon nanofibers (CNF), and mesoporous carbon (MC)) were studied. Their potential applications as catalysts for various redox reactions and electrochemical sensors were investigated. The ceria oxide layers were electrodeposited on SPCEs at various current densities and deposition time. The morphology, structure, and chemical composition in the bulk of the ceria layers were studied by SEM and EDS methods. XRD was used to identify the formed phases. The concentration, chemical composition and chemical state of the elements on the surface of studied samples were characterized by XPS. It was established that the increase of the concentration of CeCl₃ in the solution and the cathode current density strongly affected the surface structure and concentration (relation between Ce³⁺ and Ce⁴⁺, respectively) in the formed ceria layers. At low concentration of CeCl₃ (0.1M) and low values of cathode current density (0.5 mA·cm⁻²), porous samples were obtained, while with their increase, the ceria coatings grew denser. Full article

The integration of various transition metal oxides into tungsten oxide (WO₃) has been widely investigated to enhance its electrochromic (EC) performance. This approach aims to address the inherent limitations of individual metal oxides, such as poor durability, inadequate color neutrality, and restricted coloring efficiency and optical properties. The use of mixed metal oxides has emerged as a promising strategy, enabling a synergistic effect that optimizes EC performance and expands the material’s functional capabilities. In this study, we compare single-layer WO₃ films with bilayer WO₃/cobalt oxide (CoO) (denoted as W@C) composite films, focusing on their structural, morphological, and electrochromic properties. Both films were fabricated using the electrodeposition technique, with a consistent number of deposition cycles. Field emission scanning electron microscopy (FESEM) analysis revealed that the WO₃ film presented a tightly packed arrangement of nanogranules. In contrast, the bilayer W@C composite thin film exhibited a highly interconnected and porous granular structure, with morphology evolving into larger spherical aggregates. The optimized bilayer W@C composite demonstrated exceptional electrochromic performance, achieving an optical modulation of 85.0% at 600 nm and a significantly improved coloration efficiency of 96.07 cm²/C. Stability tests confirmed its remarkable durability, showing only a 1.05% decrease in optical contrast after 5000 s of operation. Additionally, a prototype electrochromic device based on the W@C film demonstrated an optical modulation of 52.13% and outstanding long-term stability, with minimal degradation in performance. Full article

This study explores a sustainable approach to developing magnetic nanocomposites by synthesizing a mixed-phase iron oxide (IO) and recycled polyamide (RPA) composite from textile waste. The RPA/IO nanocomposite’s microstructural and magnetic properties were characterized using X-ray diffraction (XRD) with Rietveld refinement, scanning, transmission electron microscopy (SEM, TEM), and vibrating sample magnetometry (VSM). The proportions of the Fe₃O₄ and γ-Fe₂O₃ phases were found to be 23.2 wt% and 76.8 wt%, respectively. SEM and TEM showed a porous, agglomerated IO surface morphology with an average particle size of 14 nm. Magnetic analysis revealed ferrimagnetic and superparamagnetic behavior, with VSM showing saturation magnetization values of 21.81 emu g⁻¹ at 5 K and 18.84 emu g⁻¹ at 300 K. Anisotropy constants were estimated at 4.28 × 10⁵ and 1.53 × 10⁵, respectively, for IO and the composite, with a blocking temperature of approximately 178 K at 300 K. These results contribute to understanding the magnetic behavior of IO and their nanocomposites, which is crucial for their potential applications in emerging technologies. Full article

The alumina, in the form of α-Al₂O₃ tabular balls, considered in this study is a high-purity form of aluminum oxide that has been fired at high temperatures (well above 1900 °C), virtually removing porosity. However, the purity and inertness of the surface of the Al₂O₃ tabular balls minimize the catalytic activity, which is why lithium doping was tried. Thus, the target of this study was the effect of doping with lithium ions in some tabular balls of Al₂O₃ (the crystalline structure is corundum) on the improvement of the catalytic properties of alumina. This study examined the impact of a lithium catalyst on the combustion of various fuels within a porous inert medium (PIM) burner. This study specifically compared low calorific gaseous fuel (e.g., biogas) combustion in a PIM burner with and without the lithium catalyst. The experimental setup comprised a gas preparation unit for mixing CNG and CO₂ to simulate biogas and a PIM burner. The PIM burner comprised Al₂O₃ spheres (13 mm diameter, 45% porosity) in a random packing configuration. Three fuels, varying in composition and lower heating value (LHV ranging from 20.771 to 27.695 MJ/m³), were combusted at air ratios ranging from 1.67 to 1.79. The results indicated that the catalyst increased peak combustion temperatures by 23.2 °C to 51.4 °C, depending on the fuel type and air ratio. Significantly higher carbon monoxide (CO) concentrations were observed without the catalyst, particularly with fuel type F1, while nitrous oxide (NOx) levels remained consistently low. Upstream flame propagation was observed in the presence of the catalyst. These findings demonstrate the potential of lithium catalysts to enhance combustion stability and reduce emissions in porous media combustion burners. Following these studies, it can be stated that Li(I) has the role of promoter of the catalytic process. Full article

Nb-Sn, V-Sn mixed-metal oxides and Nb-Si, V-Si metal oxide–silicas were successfully synthesized through a “soft” templating method, in which appropriate amounts of metal salts (either niobium(V) chloride, or vanadium(IV) oxide sulfate hydrate or tin(II) chloride dihydrate) or tetraethyl orthosilicate (TEOS) were mixed with hexadecyltrimethylammonium chloride (HDTA) or sodium dodecyl sulfate (SDS) solutions to obtain a new series of mesoporous oxides, followed by calcination at different temperatures. As-obtained samples were characterized by SEM, TEM, XRD, and UV-Vis spectra techniques. The photocatalytic activities of the samples were evaluated by degradation of methyl orange II (MO) under simulated sunlight irradiation. The effects of metal species and calcination temperature on the physicochemical characteristic and photocatalytic activity of the samples were investigated in detail. The results indicated that, compared to pure oxides, mixed-metal oxide showed superior photocatalytic performance for the degradation of MO. A maximum photocatalytic discoloration rate of 97.3% (with MO initial concentration of 0.6·10⁻⁴ mol/dm³) was achieved in 300 min with the NbSiOx material, which was much higher than that of Degussa P25 under the same conditions. Additionally, the samples were tested in the photochemical oxidation process, i.e., advanced oxidation processes (AOPs) to treat the commercial non-ionic surfactant: propylene oxide ethylene oxide polymer mono(nonylphenyl) ether (N8P7, PCC Rokita). A maximum of 99.9% photochemical degradation was achieved in 30 min with the NbSiOx material. Full article

In the mixing zone, where submarine groundwater carrying ferrous iron [Fe(II)] meets seawater with dissolved oxygen (DO), the oxidative precipitation of Fe(II) occurs at the pore scale (nm~μm), and the resulting Fe precipitation significantly influences the seepage properties at the Darcy scale (cm~m). Previous studies have presented a challenge in upscaling fluid dynamics from a small scale to a large scale, thereby constraining our understanding of the spatiotemporal variations in flow paths as porous media evolve. To address this limitation, this study simulated subsurface mixing by injecting Fe(II)-rich freshwater into a DO-rich saltwater flow within a custom-designed syringe packed with glass beads. Micro-computed tomography imaging at the representative elementary volume scale was utilized to track the development of Fe precipitates over time and space. Experimental observations revealed three distinct stages of Fe hydroxides and their effects on the flow dynamics. Initially, hydrous Fe precipitates were characterized by a low density and exhibited mobility, allowing temporarily clogged pathways to intermittently reopen. As precipitation progressed, the Fe precipitates accumulated, forming interparticle bonding structures that redirected the flow to bypass clogged pores and facilitated precipitate flushing near the syringe wall. In the final stage, a notable reduction in the macroscopic capillary number from 3.0 to 0.05 indicated a transition from a viscous- to capillary-dominated flow, which led to the construction of ramified, tortuous flow channels. This study highlights the critical role of high-resolution imaging techniques in bridging the gap between pore-scale and continuum-scale analyses of multiphase flows in hydrogeochemical processes, offering valuable insights into the complex groundwater–seawater mixing. Full article

Membrane capacitive deionization (MCDI) is an electrochemical ion separation process that combines ion-exchange membranes (IEMs) with porous carbon electrodes to enhance desalination efficiency and address the limitations of conventional capacitive deionization (CDI). In this study, a cation-exchange membrane (CEM) embedded with a metal–organic framework (MOF) was developed to effectively separate monovalent and multivalent cations in influent solutions via MCDI. To fabricate CEMs with high monovalent ion selectivity, ZIF-8 was incorporated into sulfonated poly(2,6-dimethyl-1,4-phenylene oxide) (SPPO) at various weight ratios. The resulting membranes were systematically characterized using diverse electrochemical methods. The ZIF-8-embedded CEMs demonstrated a sieving effect based on differences in ion size and hydration energy, achieving excellent permselectivity for monovalent ions. MCDI tests using the prepared CEMs showed a Na⁺ ion removal rate exceeding 99% in Na⁺/Mg²⁺ and Na⁺/Ca²⁺ mixed feed solutions, outperforming a commercial membrane (CSE, Astom Corp., Tokyo, Japan), which achieved a removal rate of 94.1%. These findings are expected to provide valuable insights for advancing not only MCDI but also other electro-membrane processes capable of selectively separating specific ions. Full article

To solve the energy crisis and environmental issues, it is essential to create effective and sustainable energy conversion and storage technologies. Traditional materials for energy conversion and storage however have several drawbacks, such as poor energy density and inadequate efficiency. The advantages of MOF-based materials, such as pristine MOFs, also known as porous coordination polymers, MOF composites, and their derivatives, over traditional materials, have been thoroughly investigated. These advantages stem from their high specific surface area, highly adjustable structure, and multifunctional nature. MOFs are promising porous materials for energy storage and conversion technologies, according to research on their many applications. Moreover, MOFs have served as sacrificial materials for the synthesis of different nanostructures for energy applications and as support substrates for metals, metal oxides, semiconductors, and complexes. One of the most intriguing characteristics of MOFs is their porosity, which permits space on the micro- and meso-scales, revealing and limiting their functions. The main goals of MOF research are to create high-porosity MOFs and develop more efficient activation techniques to preserve and access their pore space. This paper examines the porosity tunable mixed and hybrid MOF, pore architecture, physical and chemical properties of tunable MOF, pore conditions, market size of MOF, and the latest development of MOFs as precursors for the synthesis of different nanostructures and their potential uses. Full article

The self-passivating tungsten-based alloy W-11.4Cr-0.6Y (in wt.%) is a potential plasma-facing material for the first wall of future fusion reactors, which has been shown to suppress oxidation of tungsten and withstand temperatures of up to 1000 °C. In this study, the effect of Y addition on the microstructure and oxidation behavior of W-11.4Cr alloy at 1000 °C is analyzed by comparing it with W-11.4Cr-0.6Y, both prepared using identical synthesis routes. While the binary W-Cr alloy already exhibits improved oxidation resistance over pure W due to the formation of an outer Cr₂WO₆ layer, it still shows a tendency for spallation and, hence, is not protective. A continuous passivating chromia layer is only obtained with the addition of Y, and we demonstrate that it results in a 50-fold decrease in the oxide growth rate and eliminates the preferred growth of the oxide at edges seen in the binary alloy. Although a porous, complex oxide scale containing mixed oxide layers and WO₃ is formed in both cases, the addition of Y results in lower porosity, which makes the oxide scale more adherent. Full article

A plasma-reduced graphene oxide/lithium titanate oxide (PrGO/LTO) composite is prepared as an anode material to enhance the performance of lithium-ion capacitors (LICs). The PrGO/LTO composite is synthesized by mixing graphene oxide (GO) and LTO, followed by a series of freeze-drying and plasma-treatment processes. PrGO forms a porous three-dimensional (3D) structure with a large surface area, effectively preventing the restacking of PrGO while covering LTO. The GO/LTO mixing ratio is controlled to optimize the final structure for LIC applications. In lithium-ion half-cell assembly, the PrGO/LTO-based anode with an 80% mixing ratio exhibits the highest specific capacity of 73.0 mAh g⁻¹ at 20 C. This is attributed to the optimized ratio for achieving high energy density from LTO and high power density from PrGO. In a LIC full-cell comprising PrGO/LTO as the anode and activated carbon as the cathode, the energy and power densities at 1 A g⁻¹ are 40.3 Wh kg⁻¹ and 2000 W kg⁻¹, respectively, with a specific capacitance of 36.3 F g⁻¹ and capacitance retention of 94.1% after 2000 cycles. Its outstanding performance, obtained from incorporating 3D-structured PrGO with LTO at an optimized ratio, lowers the cell resistance and provides efficient lithium-ion diffusion pathways. Full article

Montmorillonite is a layered clay mineral whose modification by pillaring, i.e., insertion of oxide nanoclusters between the layers, yields porous materials of great potential in sorption and catalysis. In the present study, an unrefined industrial bentonite from Kopernica (Slovakia), containing ca. 70% of montmorillonite, was used for the preparation of Ti-, Zr-, and mixed [Ti,Zr]-pillared clay sorbents. The pillared samples were characterized with X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and N₂ adsorption at −196 °C and tested for the capacity of CO₂ sorption at 0 °C and 1 bar pressure. The experiments revealed that pillared samples sorbed at least four times more CO₂ than the parent bentonite. Of the materials tested, the sample pillared with mixed [Ti,Zr] oxide props showed the best performance, which was attributed to its superior microporosity. The results of CO₂ adsorption demonstrated that the cost-effective use of crude industrial bentonite as the sorbent precursor is a viable synthesis option. In another experiment, all pillared montmorillonites were subjected to 24 h exposure at room temperature to a flow of dry CO₂ and then tested using simultaneous thermal analysis (STA) and the mass spectrometry (MS) analysis of the evolving gases (STA/QMS). It was found that interaction with dry CO₂ reduces the amount of bound carbon dioxide and affects the processes of dehydration, dehydroxylation, and the mode of CO₂ binding in the pillared structure. Full article

A binary Fe₂O₃/Fe₃O₄ mixed nanocomposite was prepared by phyto-mediated avenue to be suited in the photo-Fenton photodegradation of methylene blue (MB) in the presence of H₂O₂. XRD and SEM analyses illustrated that Fe₂O₃ nanoparticles of average crystallite size 8.43 nm were successfully mixed with plate-like aggregates of Fe₃O₄ with a 15.1 nm average crystallite size. Moreover, SEM images showed a porous morphology for the binary Fe₂O₃/Fe₃O₄ mixed nanocomposite that is favorable for a photocatalyst. EDX and elemental mapping showed intense iron and oxygen peaks, confirming composite purity and symmetrical distribution. FTIR analysis displayed the distinct Fe-O assignments. Moreover, the isotherm of the developed nanocomposite showed slit-shaped pores in loose particulates within plate-like aggregates and a mesoporous pore-size distribution. Thermal gravimetric analysis (TGA) indicated the high thermal stability of the prepared Fe₂O₃/Fe₃O₄ binary nanocomposite. The optical properties illustrated a narrowing in the band gab (Eg = 2.92 eV) that enabled considerable absorption in the visible region of solar light. Suiting the developed binary Fe₂O₃/Fe₃O₄ nanocomposite in the photo-Fenton reaction along with H₂O₂ supplied higher productivity of active oxidizing species and accordingly a higher degradation efficacy of MB. The solar-driven photodegradation reactions were conducted and the estimated rate constants were 0.002, 0.0047, and 0.0143 min⁻¹ when using the Fe₂O₃/Fe₃O₄ nanocomposite, pure H₂O₂, and the Fe₂O₃/Fe₃O₄/H₂O₂ hybrid catalyst, respectively. Therefore, suiting the developed binary Fe₂O₃/Fe₃O₄ nanocomposite and H₂O₂ in photo-Fenton reaction supplied higher productivity of active oxidizing species and accordingly a higher degradation efficacy of MB. After being subjected to four photo-Fenton degradation cycles, the Fe₂O₃/Fe₃O₄ nanocomposite catalyst still functioned admirably. Further evaluation of Fe₂O₃/Fe₃O₄ nanocomposite in photocatalytic remediation of contaminated water using a mixture of MB and pyronine Y (PY) dyestuffs revealed substantial dye photodegradation efficiencies. Full article

The mixing of terrestrial groundwater and seawater creates dynamic reaction zones in intertidal areas, where land-derived Fe(II) is oxidized to Fe(III) and then precipitates as Fe hydroxides at the groundwater–seawater interface. These hydrogeochemical processes contribute to the formation of iron bands at the saltwater wedge (SW) and beneath the upper saline plume (USP). This study provides a comprehensive review of physical and geochemical processes at field scale in coastal areas, explores the impact of mineral precipitation on pore structure at pore scale, and synthesizes reactive transport modeling (RTM) approaches for illustrating continuum-scale soil physio-chemical parameters during the evolution of porous media. Upon this review, knowledge gaps and research needs are identified. Additionally, challenges and opportunities are presented. Therefore, we reach the conclusion that the incorporation of observational data into a comprehensive physico-mathematical model becomes imperative for capturing the pore-scale processes in porous media and their influence on groundwater flow and solute transport at large scales. Additionally, a synergistic approach, integrating pore-scale modeling and non-invasive imaging, is equally essential for providing detailed insights into intricate fluid–pore–solid interactions for future studies, as well as facilitating the development of regional engineering-scale models and physio-chemical coupled models with diverse applications in marine science and engineering. Full article