Search Results (1,310)

This review presents recent results focused on immobilization of zeolites onto inexpensive aluminum substrate using plasma electrolytic oxidation (PEO) processing in various electrolyte solutions applying different electrical regimes. PEO is recognized as a useful technique for the formation of oxide coatings with photocatalytic properties on various metals and alloys. Thin film photocatalysts are more practical than powder/nanoparticle photocatalysts because the photocatalyst does not need to be filtered/separated after the wastewater degradation treatment, which is an expensive and time-consuming process. Addition of zeolites to supporting electrolyte solutions influences structural, morphological and chemical properties of formed oxide coatings. Furthermore, introduction of zeolites loaded with cerium through an ion-exchange procedure is investigated. It is shown that the addition of both parent zeolites and Ce-exchanged zeolites is beneficial for photocatalytic decomposition of model organic pollutant (methyl orange). The most promising results are obtained under ultra-low duty cycle electrical conditions with Ce-exchanged 13X zeolite added to the electrolyte, where about 60% of the model organic pollutant is decomposed during 6 h of treatment under simulated sunlight irradiation (16,000 lx) for 3 cm² surface area of sample exposed to irradiation. Full article

To overcome the low strength of conventional polytetrafluoroethylene/aluminum (PTFE/Al) reactive materials and the insufficient reaction efficiency of aluminum, this study introduces highly reactive aluminum–cerium alloys (Al-Ce-1#, -2#, and -3#, with Ce contents of 30, 50, and 70%, respectively; the primary phase in Al-Ce-3# is Al₂Ce) with a multiscale structural design (comprising both micron-sized and nano-sized particles) into an ammonium perchlorate (AP) matrix. Al/AP reactive materials and Al-Ce/AP reactive materials with varying Ce contents were prepared. The thermal decomposition characteristics, dynamic mechanical properties, and impact ignition behavior were systematically investigated using differential scanning calorimetry (DSC) and split Hopkinson pressure bar (SHPB) experiments. The results demonstrate that the addition of Al₂Ce significantly alters the thermal decomposition process of AP, substantially lowering its decomposition temperature (by approximately 69 °C) and promoting concentrated exothermic decomposition. SHPB tests reveal that Al₂Ce/AP composites exhibit higher dynamic yield strength and flow stress than the Al/AP, accumulating faster strain energy density under impact loading, which indicates a more violent fragmentation failure mode. This enhanced mechanical failure behavior, which provides highly reactive interfaces and promotes hotspot formation, synergizes with the catalytic effect of Al₂Ce on AP decomposition. Together, these mechanisms jointly improve the impact ignition sensitivity of the material, significantly lowering its ignition threshold and shortening its combustion duration. This study confirms that Al₂Ce/AP is a novel reactive material combining excellent dynamic mechanical properties with outstanding impact reactivity, providing theoretical and technical support for the application of highly reactive rare-earth aluminum alloys in aluminum-based reactive materials. Full article

Rare-earth elements (REEs), which include the entire lanthanide series together with scandium and yttrium, have unique electronic configurations and coordination chemical properties that provide them with special magnetic, optical, and redox abilities. Generally used for diagnostic imaging and theranostic applications, increasing evidence emphasizes their potential as direct anticancer agents. This review aims to present a thorough investigation of the studies published in the last ten years that focus on the intrinsic anticancer properties of REE-based molecular complexes and nanostructures, without discussing their recognized imaging functions. Rare-earth compounds exhibit selective cytotoxicity against malignant cells via mechanisms that mainly include modulations in the generation of reactive oxygen species, mitochondrial dysfunctions, interaction with DNA molecules, apoptosis, and ferroptosis induction, as well as radiosensitization. Molecular complexes that are based on the trivalent coordination chemistry of REEs enable them to target biomolecules like DNA and serum albumin. Nanostructured systems, on the other hand, render tumors more responsive to treatment by improving the cellular uptake, enabling surface functionalization, and controlling ROS generation. Terbium, thulium, yttrium, scandium, ytterbium, cerium, erbium, dysprosium, and europium show different levels of anticancer activity in both in vitro and in vivo cancer models. They often exert more toxicity in tumor cells than in normal tissues, thus exhibiting selective anticancer effects. The findings collectively underscore the therapeutic potential of REE-based compounds as novel metal-based anticancer agents and advocate for additional mechanistic and translational research to enhance their clinical applicability. Full article

Cerium dioxide (CeO₂) has emerged as a structurally versatile oxide for dye-wastewater purification because its architecture, porosity, and surface accessibility can be tuned over a wide range while maintaining good chemical stability and environmental compatibility. Recent studies show that template-free or low-template routes can generate porous, mesoporous, multilayered, and flower-like CeO₂ architectures with rapid dye uptake and, in some systems, adsorption-assisted photocatalytic removal. However, CeO₂-based dye removal has often been discussed either within broad surveys of environmental applications or from composition-centered viewpoints, whereas the more fundamental question is how synthesis route controls architecture formation and how architecture, in turn, governs adsorption and subsequent removal behavior. This mini-review addresses that question from a morphology-centered perspective. It first examines template-free and low-template routes for constructing structured CeO₂, then discusses how porosity, hierarchical assembly, and surface accessibility regulate adsorption kinetics and equilibrium capacity in dye-containing aqueous systems. It further considers adsorption-assisted photocatalytic removal and argues that dark adsorption should be regarded as the structural first step rather than a secondary contribution. On this basis, the review shows that rare-earth doping in these systems is most usefully understood as a secondary tuning strategy that refines an already favorable host architecture by modifying surface interaction, optical response, or reactive-species generation. Overall, the available evidence indicates that CeO₂-based dye-wastewater purification is most meaningfully interpreted through a route–architecture–function framework in which morphology defines the host, adsorption organizes the local reaction environment, and doping serves mainly as structure-assisted tuning. This perspective shifts the design logic of CeO₂ from empirical performance optimization toward rational structure-directed construction of integrated removal platforms. Full article

Emission control of diesel particulate matter (soot) combustion is important for environmental reasons. Catalysts are indispensable for optimizing these processes, as they significantly reduce the combustion temperature. In this work, mixed oxides (cerium–copper, cerium–manganese, and cerium–molybdenum) were prepared by co-precipitation under reasonably similar synthesis conditions, and the effects of their chemical composition on diesel soot combustion were evaluated using the Printex U model particulate. Thermogravimetric analysis (TG/DTG) and temperature-programmed oxidation coupled with mass spectrometry (TPO/MS) were employed for activity characterization. Structural analyses revealed the presence of nanocrystalline phases containing CeO₂ (fluorite), CuO (monoclinic), Mn₂O₃ (cubic), and MoO₃ (orthorhombic), depending on the catalyst composition. The most effective catalysts exhibited an equimolar oxide composition (CeO₂–MO_x). Tests performed at optimized calcination temperatures and with the addition of promoters led to the identification of optimal combustion conditions. The highest activity, corresponding to the lowest combustion temperature, was observed in the following order: CeO₂–Mn₂O₃ > CeO₂–CuO > CeO₂–MoO₃, with values of 382, 409, and 425 °C, respectively, under tight-contact conditions at a Printex U:catalyst ratio of 1:20. With the addition of a 10% Ag₂O promoter, the CeO₂–Mn₂O₃ catalyst further reduced the oxidation temperature to 376 °C. Reusability tests generally indicated a 10–20% decrease in catalytic activity by the third reaction cycle. Full article

Nanoparticle powders of a Ce_1−xRu_xO₂ mixed oxide (3.0% w/w), were synthesized to be used as catalytic supports, on which Pt and Ir nanoparticles were deposited as the active phase. The catalytic supports were prepared through a route involving microwave heating, while the Pt or Ir nanoparticles were incorporated via the wet incipient method. The {Pt, Ir/Ce_1−xRu_xO₂} catalytic systems were successfully tested as catalysts for low-temperature CO oxidation. To provide adequate support to our results, the compounds were characterized by SEM, EDS, XRD, DRS-UV-vis, and XPS techniques. In addition, BET isotherms were carried out to determine specific surface area features. The CO oxidation evolution was tested in the range of 25–350 °C. Both Pt and Ir supported Ce_1−xRu_xO₂ catalysts that remarkably improved the CO oxidation, reaching and sustaining 100% conversion from 125 °C onwards. Remarkably, the mixed oxide support, by itself, showed outstanding performance, achieving 100% conversion to CO₂, at a temperature of 225 °C. Full article

Cerium oxide nanoparticles (CeO₂NPs) possess unique physicochemical properties that make them promising compounds for medical and industrial applications. However, variations in synthesis methods, particle size, and surface characteristics may influence their potential toxicity. This study provides a comparative analysis of CeO₂NPs synthesized via three methods (citric, dextran, and uncoated modifications) to evaluate their toxicity, antioxidant mechanisms, and genoprotective potential using a panel of Escherichia coli-based lux-biosensors. Our data indicate that all of the tested CeO₂NPs exhibit high biocompatibility with no significant toxicity or genotoxicity at physiological concentrations (10⁻⁴–10⁻² M). The citrate-modified nanoparticles demonstrated pronounced catalase-mimetic activity, acting as the most effective scavengers against hydrogen peroxide. Conversely, the dextran-modified nanoparticles exhibited the highest antimutagenic potential, reducing dioxidine-induced DNA damage by over 56%. Thus, beyond establishing biocompatibility, this study highlights the potential of using specific CeO₂NP modifications for targeted therapy depending on the oxidative pathway involved. This suggests their potential for application as antioxidant and antimutagenic agents in both human and veterinary medicine. Full article

Red Amaranth (RA) Azo dye is a persistent pollutant in wastewater and stands as a toxicological risk, which has led to the development of effective methods for its removal and photocatalytic degradation. Therefore, CeO₂ nanoparticles were synthesized by a controlled precipitation method, and Ultraviolet-Visible (UV–Vis) analysis and Tauc plots yielded a band gap of ~3.24 eV. The CeO₂ nanoparticles showed the fluorite cubic phase, and nearly spherical particles with an average size of ~10 nm. Nitrogen physisorption revealed a type IV isotherm with a Brunauer–Emmett–Teller (BET) surface area of 85.27 m²·g⁻¹ and a total pore volume of 0.27 cm³·g⁻¹, indicating a mesoporous structure and high surface accessibility. The chemical behavior showed Ce and O, consistent with phase purity. Photocatalytic performance was evaluated in 20 ppm aqueous solution of RA under 365 nm UV irradiation (LED 100 W), with a temperature of ~20 °C and a 15 min dark adsorption step. Concentration decay was followed at λ_max = 520 nm by Lambert–Beer. The degradation efficiency η and pseudo-first-order kinetic were obtained from ln(C₀/C_t) vs. time. In addition, chemical oxygen demand (COD) tests were performed on RA solution before and after photodegradation, showing a COD reduction of ~85% (from 19.8 to 3 mg O₂·L⁻¹), which corroborates mineralization beyond chromophore bleaching. Under [C₀ = 20 mg·L⁻¹] and [m_cat = 1.0 g·L⁻¹], CeO₂ achieved [RA = 90% at 180 min, k = 0.0125 min⁻¹]. These results demonstrate that CeO₂ is an effective photocatalyst for RA degradation under UV-A irradiation, integrating adsorption, kinetic behavior, and mineralization performance into a coherent structure–property relationship. Full article

Purpose: Pure three-dimensional (3D)-printed resin for denture base shows strength in comparison with the conventional heat-cured materials. The purpose of this study was to assess how physical and mechanical properties of 3D-printed denture base resins are affected by the addition of cerium zirconium oxide nanofibers (CeZrO₄ NFs), which have a unique combination of thermophysical and mechanical properties. Materials and Methods: The specimens were digitally created utilizing Microsoft Corporation’s 3D builder software through computer-aided design. To meet the test criteria for transverse strength, impact strength, hardness, radiopacity, and degree of conversion (DC), specimens were designed and printed with specific dimensions according to the relevant standards. The 3D-printed denture base resin was mixed with CeZrO₄ NFs (diameter: 300–800 nm, length: 2–10 µm) at weight percentages of 0.5, 1.0%, 1.5%, 2%, and 2.5%. The data were analyzed using Tukey’s post hoc test (α = 0.05) and ANOVA. Field emission scanning electron microscopy (FESEM) and energy dispersive X-ray spectroscopy (EDX) were used to evaluate surface morphologies of the composites and nanofibers, and the dispersion of the NFs within the resin matrix respectively. Results: The results demonstrated that compared with those of the control group, the average transverse strength, impact strength, and hardness values of the CeZrO₄ NF reinforcement groups significantly increased up to a nanofiller concentration of 1.5 wt.%., whereas those of the other reinforcement groups significantly decreased. For example, the impact strength significantly increased from 5.84 kJ/m² (0 wt.%) to the maximum value 8.76 kJ/m² at 1.0 wt.% CeZrO₄ NF. On the other hand, the Shore D hardness increased from 80.84 for the control group to the maximum value 83.27 at 1.5 wt.% CeZrO₄ NF. The radiopacity increased as the NF concentration increased. Although Fourier transform infrared (FTIR) spectroscopy analysis did not show any noticeable change in the chemical structure of the resin after incorporating the NFs, there was a notable improvement in the DC of the nanocomposites with NF concentrations of 0.5, 1.0 and 1.5 wt.%. Energy dispersive X-ray spectroscopy (EDX) and field emission scanning electron microscopy (FESEM) showed evidence of uniform distribution of the CeZrO₄ NFs in the 3D-printed specimens. Conclusions: The properties of the denture bases fabricated from 3D-printed resin were enhanced by the addition of 0.5%, 1 wt.% and 1.5 wt.% CeZrO₄-milled NFs, though the latter two concentrations produced the most significant results. Full article

The hematite phase decorated with iron-doped cerium oxide nanoparticles (F@FC) was precipitated from cerium and iron oxalate intermediate products. The photocatalytic composite of graphitic carbon nitride (gCN) and F@FC was prepared by a simple method involving mixing the two components, followed by thermal treatment at 400 °C. According to electron microscopy, F@FC is composed of a submicron iron oxide (hematite) phase decorated with iron-doped cerium oxide nanoparticles deposited on gCN substrate. A hierarchically structured composite was observed instead of a simple mechanical mixture of α-Fe₂O₃, Fe-CeO₂, and gCN. To observe two types of degradation activity, photocatalytic and Photo-Fenton degradation activity, Rhodamine B (RhB) was applied as the model water pollutant. The influence of the amount of photocatalyst, the RhB concentration, the presence of cations and anions, the pH, and the effect of e⁻, h⁺, •OH, and •O₂⁻ scavenging reactants were studied. The Photo-Fenton degradation exhibited high efficiency across the entire tested pH range, whereas photocatalytic degradation showed comparable activity only at acidic pH. The F@FC-gCN composite catalyst exhibited a high degree of recyclability. The degradation pathways of photocatalytic and Photo-Fenton reactions were suggested by HPLC-MS analysis of the reaction products. A notable finding of this study was the observation that the green-yellow, fluorescent intermediate Rhodamine 110 was formed during the photocatalytic degradation of RhB. However, the high reactivity of the generated •OH radicals during Photo-Fenton degradation has been demonstrated to inhibit the formation of intermediate Rhodamine 110. Full article

This study presents a comprehensive comparative analysis of the performance, combustion, and emission characteristics of a single-cylinder, four-stroke spark-ignition engine fueled by commercial gasoline and raw biogas enhanced with cerium oxide (CeO₂) nanoparticles. Raw biogas containing 58% methane was tested without carbon dioxide removal to reflect practical rural applications, while CeO₂ nanoparticles were ultrasonically dispersed in the fuel to promote homogeneous suspension and catalytic activity. Experiments were conducted under wide-open and part-throttle conditions across a range of engine speeds, with simultaneous measurement of brake thermal efficiency, brake-specific fuel consumption, volumetric efficiency, in-cylinder pressure, heat release rate, combustion phasing, and regulated emissions. The results showed that while gasoline consistently outperformed biogas in torque and power due to its higher heating value and flame speed, the addition of CeO₂ significantly reduced the performance gap. For the biogas mode, CeO₂ addition increased brake thermal efficiency by up to 5%, lowered brake-specific fuel consumption by up to 8%, and shifted the start of main combustion to earlier crank angles, indicating faster and more complete combustion, particularly at high loads where higher temperatures activate CeO₂’s catalytic behavior. Emission analysis revealed that CeO₂-blended biogas reduced carbon monoxide emissions by approximately 25% and unburned hydrocarbons by up to 55% compared with gasoline, while nitrogen oxide emissions were consistently 15–22% lower. These reductions were observed across both wide-open and part-throttle conditions, confirming improved combustion completeness and lower peak flame temperatures. These improvements are attributed to CeO₂’s oxygen-storage capability, catalytic oxidation activity, and enhanced thermal conductivity, which collectively strengthen combustion completeness and cyclic stability. The findings demonstrate that nanoparticle-enhanced biogas can substantially improve the environmental and operational viability of spark-ignition engines, offering a practical pathway for integrating renewable gaseous fuels into existing transportation systems. Full article

Microstructural and morphological effects of cobalt (Co), nickel (Ni), and cerium (Ce) microalloying on the SAC305 lead-free solder alloy were investigated, with emphasis on the solidification behavior under slow cooling conditions. Although the individual effects of these elements have been previously reported, their combined influence remains scarcely addressed. Thermal behavior, elemental composition, and surface integrity of the solder joints were analyzed. The addition of Co, Ni, and Ce resulted in a significant shift of the onset temperature during cooling, indicating reduced undercooling. Microalloying led to a transformation of the intermetallic layer (IML) morphology from scalloped to planar, and a 60% reduction in the number of shrinkage voids. The average β-Sn grain size decreased by 37.5%, while the eutectic area increased from 32% to 38%. The substitution of Cu atoms by Co and Ni within the Cu₆Sn₅ lattice formed thermodynamically stable (Cu,Co,Ni)₆Sn₅ phases. These findings demonstrate that the synergistic effect of Co, Ni, and Ce microadditives effectively refines the microstructure, suppresses undercooling, and enhances the overall reliability of SAC305 solder joints. Full article

Zinc-based coatings are insufficient as surface coatings; they corrode rapidly and can cause long-term damage to subsea pipelines and other instruments. Therefore, this research was undertaken by manufacturing a sacrificial nano-reinforced Zn coating combined with additives via electrodeposition onto a mild steel S235 substrate, which provides excellent corrosion resistance under severe marine conditions. The electrodeposited coatings were characterized using SEM/EDS and XRD, revealing the effective incorporation of cerium oxide nanoparticles and high-quality graphene (Gr) in the zinc matrix. Vickers microhardness measurements, mechanical resilience, and surface roughness of the Zn-CeO₂-Gr coating showed an inverse correlation between improved microhardness (+65.85%) and mechanical resilience (+31.49%), while surface roughness decreased (−81.48%) compared to pure zinc electrodeposited coatings. These characteristics indicate grain refinement and greater reliability under mechanical stress. Electrochemical impedance spectroscopy (EIS) and DC polarization measurements indicate a significant improvement in corrosion resistance compared to pure zinc, due to the synergistic effect between graphene and cerium oxide nanoparticles, which reduces the cathodic activity of the surface. These findings offer promising applications for cutting-edge materials in saline environments. Full article

The oxygen evolution reaction (OER), a key half-reaction in electrochemical water splitting, is limited by sluggish multi-electron transfer kinetics, starting extensive research into efficient, low-cost nanoscale electrocatalysts, particularly those based on nickel, cobalt, and iron, as well as mixed-metal, hybrid, and heteroatom-doped carbon-based metal-free systems, as presented here. Ni- and Co-based electrocatalysts show high efficiency for alkaline OER due to optimized nanostructures, surface modifications, heterostructure design, and multi-metal doping, which enhance activity, stability, and electronic properties. Their performance relies on precise atomic-level control of structure and synergistic interactions, enabling them to approach or rival noble-metal catalysts. Iron-based electrocatalysts are also promising due to their abundance, low cost, and flexible redox chemistry, forming active iron oxyhydroxide species during operation; however, their low conductivity requires structural and electronic optimization. Beyond Fe, Ni, and Co, copper-based compounds, zeolitic imidazolate framework-derived structures, and manganese phosphide–cerium oxide composites offer enhanced oxygen vacancies, tunable structures, and strong interfacial synergy. Furthermore, heteroatom-doped carbon materials incorporating nitrogen, phosphorus, or sulfur improve catalytic activity by modifying electronic structure, creating active sites, and enhancing charge transfer. Overall, careful control of composition, structure, and electronic properties enables the development of efficient, durable, and scalable noble-metal-free catalysts for OER. Full article

This study evaluates the effects of Al₂O₃ and CeO₂ nanoparticles as additives to standard diesel and biodiesel fuels on the combustion and emissions characteristics of a CR diesel engine with split injection (pilot and main injections). Three nanoparticle dosing levels (50 ppm, 100 ppm, and 150 ppm) were compared with undoped standard diesel and biodiesel fuels. The results showed that the presence of both Al₂O₃ and CeO₂ in biodiesel increased the ignition delay of the pilot fuel by about 8.0% at low load and about 3.5% at high load. The addition of both nanoparticles to diesel and biodiesel fuels had an insignificant effect on the main injection fuel’s ignition delay, MBF50 position and combustion duration. The thermal efficiency was up to 1.0% lower. Al₂O₃ additive in diesel had no significant effect on NO_x emissions. CO emissions were higher by 4.4–7.5% in most cases. The Al₂O₃ additive in biodiesel reduced NO_x emissions by an average of 38%, 17.1%, and 9.4% at low, medium, and high engine loads, respectively. The reduction in CO emissions averaged 15%. The addition of CeO₂ nanoparticles to diesel fuel reduced NO_x emissions by 22.5%, 8.5%, and 3.1% on average across the corresponding load ranges. When the engine was operated on CeO₂-doped biodiesel, NO_x emissions were lower by an average of 25.7%, 9.6%, and 2.5% at low, medium, and high loads, respectively. Adding CeO₂ nanoparticles to diesel fuel increased CO emissions, whereas adding them to biodiesel significantly reduced CO emissions. Full article