Search Results (706)

Dry reforming of methane and ethanol is a promising catalytic process for the conversion of carbon dioxide and hydrocarbon feedstocks into synthesis gas (H₂/CO), which serves as a key platform for the production of fuels and chemicals. Over the past decade, substantial progress has been achieved in the design of catalysts with enhanced activity and stability under the demanding conditions of these strongly endothermic reactions. This review summarizes the latest developments in catalyst systems for DRM and EDR, including Ni-based catalysts, perovskite-type oxides, MOF-derived materials, and high-entropy alloys. Particular attention is given to strategies for suppressing carbon deposition and preventing metal sintering, such as oxygen vacancy engineering in oxide supports, rare earth and transition metal doping, strong metal–support interactions, and morphological control via core–shell and mesoporous architectures. These approaches have been shown to improve coke resistance, maintain metal dispersion, and extend catalyst lifetimes. The review also highlights emerging concepts such as multifunctional hybrid systems and innovative synthesis methods. By consolidating recent findings, this work provides a comprehensive overview of current progress and future perspectives in catalyst development for DRM and EDR, offering valuable guidelines for the rational design of advanced catalytic materials. Full article

An overview of the Common Rail (CR) diesel engine challenges and of the promising state-of-the-art solutions for addressing them is provided. The different CR injector driving technologies have been compared, based on hydraulic, spray and engine performance for conventional diesel combustion. Various injection patterns, high injection pressures and nozzle design features are analyzed with reference to their advantages and disadvantages in addressing engine issues. The benefits of the statistically optimized engine calibrations have also been examined. With regard to the combustion strategy, the role of a CR engine in the implementation of low-temperature combustion (LTC) is reviewed, and the effect of the ECU calibration parameters of the injection on LTC steady-state and transition modes, as well as on an LTC domain, is illustrated. Moreover, the exploitation of LTC in the last generation of CR engines is discussed. The CR apparatus offers flexibility to optimize the engine calibration even for biofuels and e-fuels, which has gained interest in the last decade. The impact of the injection strategy on spray, ignition and combustion is discussed with reference to fuel consumption and emissions for both biodiesel and green diesel. Finally, the electrification of CR diesel engines is reviewed: the effects of electrically heated catalysts, electric supercharging, start and stop functionality and electrical auxiliaries on NO_x, CO₂, consumption and torque are analyzed. The feasibility of mild hybrid, strong hybrid and plug-in CR diesel powertrains is discussed. For the future, based on life cycle and manufacturing cost analyses, a roadmap for the automotive sector is outlined, highlighting the perspectives of the CR diesel engine for different applications. Full article

Per- and polyfluoroalkyl substances (PFAS) are a diverse group of synthetic fluorinated compounds widely used in industrial and consumer products due to their exceptional thermal stability and hydrophobicity. However, these same properties contribute to their environmental persistence, bioaccumulation, and potential adverse health effects, including hepatotoxicity, immunotoxicity, endocrine disruption, and increased cancer risk. Traditional water treatment technologies, such as coagulation, sedimentation, biological degradation, and even advanced membrane processes, have demonstrated limited efficacy in removing PFAS, as they primarily separate or concentrate these compounds rather than degrade them. In response to these limitations, photoassisted processes have emerged as promising alternatives capable of degrading PFAS into less harmful products. These strategies include direct photolysis using UV or VUV irradiation, heterogeneous photocatalysis with materials such as TiO₂ and novel semiconductors, light-activated persulfate oxidation generating sulfate radicals, and photo-Fenton reactions producing highly reactive hydroxyl radicals. Such approaches leverage the generation of reactive species under irradiation to cleave the strong carbon–fluorine bonds characteristic of PFAS. This review provides a comprehensive overview of emerging photoassisted technologies for PFAS removal from water, detailing their fundamental principles, degradation pathways, recent advancements in material development, and integration with hybrid treatment processes. Moreover, it discusses current challenges related to energy efficiency, catalyst deactivation, incomplete mineralization, and scalability, outlining future perspectives for their practical application in sustainable water treatment systems to mitigate PFAS pollution effectively. Full article

In recent years, one of the major problems facing humanity has been the contamination of the environment by various organic pollutants, with some of them exhibiting environmental persistence or pseudo-persistence. For this reason, it is necessary today, more than ever, to find new and effective methods for degrading these persistent pollutants. Transition metal selenides (TMSes) have emerged as a versatile and promising class of catalysts for the degradation of organic pollutants through various advanced oxidation processes (AOPs). The widespread use of these materials lies in the desirable characteristics they offer, such as unique electronic structures, narrow band gaps, high electrical conductivity, and multi-valent redox behavior. This review comprehensively examines recent progress in the design, synthesis, and application of these TMSes—including both single- and composite systems, such as TMSes/g-C₃N₄, TMSes/TiO₂, and heterojunctions. The catalytic performance of these systems is being highlighted, regarding the degradation of organic pollutants such as dyes, pharmaceuticals, antibiotics, personal care products, etc. Further analysis of the mechanistic insights, structure–activity relationships, and operational parameter effects are critically discussed. Emerging trends, such as hybrid AOPs combining photocatalysis with PMS or electro-activation, and the challenges of stability, scalability, and real wastewater applicability are explored in depth. Finally, future directions emphasize the integration of multifunctional activation methods for the degradation of organic pollutants. This review aims to provide a comprehensive analysis and pave the way for the utilization of TMSe catalysts in sustainable and efficient wastewater remediation technologies. Full article

In this study, we investigated the influence of polymer nature and support characteristics on the performance of Pd-based heterogeneous catalysts. Catalysts were prepared via sequential adsorption of poly(4-vinylpyridine) (P4VP) or chitosan (CS) and palladium ions onto MgO and SBA-15 supports under ambient conditions. The resulting hybrid materials were characterized by IR spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectra (XPS). TEM analysis revealed that Pd nanoparticles with an average size of 2–3 nm were well-dispersed on P4VP/MgO, while larger and less uniformly distributed particles (8–10 nm) were observed on SBA-15-based systems. Catalytic tests in the hydrogenation of 2-propen-1-ol, phenylacetylene, and 2-hexyn-1-ol under mild conditions (40 °C, 1 atm H₂, ethanol) demonstrated that both the support and polymer type significantly influence activity and selectivity. P4VP-modified catalysts outperformed CS-containing analogs in all reactions. MgO-based systems showed higher activity and selectivity in 2-propen-1-ol hydrogenation compared to SBA-15-based catalysts. The 1%Pd–P4VP/MgO catalyst exhibited the best performance, with a reaction rate of 5.2 × 10⁻⁶ mol/s, 83.4% selectivity to propanol, and stable activity over 30 consecutive runs. In phenylacetylene and 2-hexyn-1-ol hydrogenation, all catalysts showed high selectivity to styrene (93–95%) and cis-2-hexen-1-ol (96–97%), respectively. The incorporation of P4VP polymer into the Pd/MgO catalyst leads to smaller and better-distributed palladium particles, resulting in enhanced catalytic activity and stability during hydrogenation reactions. These results confirm that the choice of polymer modifier and inorganic support must be tailored to the specific reaction, enabling the design of highly active and selective polymer-modified Pd catalysts for selective hydrogenation processes under mild conditions. Full article

In this study, we report, for the first time, the tribo-catalytic degradation of methyl orange (MO) using Cu/Al₂O₃ nanoparticles under mechanical stirring conditions. The hybrid catalyst was synthesized via a wet impregnation method and characterized through different techniques, confirming structural integrity and compositional uniformity. When subjected to friction generated by a PTFE-coated magnetic stir bar, Cu/Al₂O₃ nanoparticles exhibited high tribo-catalytic activity, achieving up to 95% MO degradation within 10 h under dark conditions. The observed activity surpasses that of alumina alone and is attributed to the synergistic effects between copper and alumina, facilitating charge separation and enhancing reactive oxygen species (ROS) formation. Tribo-catalytic efficiency was further influenced by stirring speed and contact area, confirming the key role of mechanical friction. Reusability tests demonstrated stable performance over five cycles, highlighting the material’s durability and potential for practical environmental remediation applications. Full article

To enhance the formation of hydroxyl radicals (•OH) when polishing single crystal silicon carbide (SiC), this study proposes a catalytic-assisted polishing approach based on a Fe₃O₄/ZnO/graphite hybrid system. Firstly, methyl orange degradation experiments were conducted using Fe₃O₄/ZnO/graphite hybrid catalysts. Secondly, a resin-based abrasive tool embedded with the Fe₃O₄/ZnO/graphite hybrid was developed. Subsequently, polishing experiments under dry, water, and hydrogen peroxide conditions were performed based on the abrasive tool. The corresponding surface roughness (Sa) were 26.51 nm, 12.955 nm and 4.593 nm, separately. The material removal rate were 0.733 mg/h (1.586 μm/h), 2.800 mg/h (6.057 μm/h) and 4.733 mg/h (10.239 μm/h), respectively. The results demonstrate that the Fe₃O₄/ZnO/graphite hybrid synergistically enhanced •OH generation through Fenton reactions and tribocatalysis of ZnO. Therefore, the increased •OH productivity contributes to SiC oxidation and SiO₂ removal, improving both polishing efficiency and surface finish. The catalytic-assisted polishing provides a novel approach for the high-efficiency ultra-precision machining for SiC. Full article

The increasing occurrence of antibiotics in water bodies all over the world has raised concerns because of the prospect that they might have genotoxic and antibiotic-resistant consequences in both people and aquatic creatures. In particular, it has been discovered that the construction of hybrid photocatalytic composite materials has greater antibiotic degradation efficiencies. The hybrid photocatalysts deliver improved photoabsorbance, charge separation, transfer, and redox characteristics, as well as enhanced photostability and rapid recovery, due to their optimal characteristic qualities, including superior structural, surface, and interfacial properties. Additionally, metal-based electrocatalysts have garnered notable attention in the field of water splitting as they are low-cost, standard and have the potential to be used in green and clean technology. MXene, a family of two-dimensional transition metal carbides and nitrides, was discovered in 2011 due to its high conductivity, large surface area, and abundance of catalytically active sites. By making hybrid structures of MXene with other materials, which have shown better electrocatalytic activity than pure MXenes. The two half-cell processes involved in water electrolysis are the oxygen generation at the anode site and the hydrogen production at the cathode site. This review paper provides a summary of the latest advancements in the design of several hybrid systems, catalysts and their effectiveness in degrading a range of newly discovered antibiotic pharmaceutical pollutants in aquatic settings, as well as recent developments on the use of MXenes and MXene-based hybrid structures such as OER, HER, and bifunctional electrocatalysts for general water splitting. Full article

Room-temperature sodium–sulfur (RT Na-S) batteries hold great potential in the field of large-scale energy storage due to their high theoretical energy density and low cost of raw materials. However, the inherent low conductivity, notorious shuttling, and sluggish kinetics of cathode materials cause the loss of active substances and capacity delay, hindering the practical application of RT Na-S batteries. Owing to their low cost, variable oxidation states, and unsaturated d orbitals, transition metal (TM)-based catalysts have been extensively studied in circumventing the above shortcomings. Herein, the review first elaborates on the reaction mechanisms and current challenges of RT Na-S batteries. Subsequently, the role and function mechanism of TM-based catalysts (including single/dual atoms, nanoparticles, compounds, and heterostructures) in RT Na-S batteries are described. Specifically, based on the theories of electronic transfer and atomic orbital hybridization, the interaction mechanism between TM-based catalysts and polysulfides, as well as the catalytic performance, are systematically discussed and summarized. Finally, a discussion on the challenges and future research perspectives associated with TM-based catalysts for RT Na-S batteries is provided. Full article

Phenol is a refractory organic pollutant that is difficult to degrade in wastewater treatment, and efficiently and stably degrading phenol presents a significant challenge. In this study, iron-doped humic acid-based nitrogen–carbon materials were prepared to activate peroxymonosulfate (PMS) for the degradation of phenol. The Fe-N-C/PMS system achieved a phenol degradation rate of 99.71%, which follows a first-order kinetic model, with the reaction rate constant of 0.1419 min⁻¹. The phenol degradation rate remained above 92% in inorganic anions (Cl⁻, SO₄²⁻, HCO₃⁻) and humic acid and the system maintained a 100% phenol removal rate over a wide pH range (3–9). The iron in the catalyst predominantly exists in the forms of Fe⁰ and Fe₃C, and Fe⁰, Fe²⁺/Fe³⁺ are the main active sites that promote PMS activation during the reaction. Additionally, Fe-N-C has a large specific surface area (1041.36 m²/g). Quenching experiments and electron spin resonance (ESR) spectroscopy detected the active free radicals in the Fe-N-C/PMS system: SO₄^•−, •OH, O₂^•−, and ¹O₂. The mechanism for phenol degradation was discussed, involving radical pathways (SO₄^•−, •OH, O₂^•−) and the non-radical pathway (¹O₂), in the Fe-N-C/PMS system activated by Fe⁰, Fe²⁺/Fe³⁺, sp² hybridized carbon, C-O/C-N, C=O, and graphitic nitrogen active sites. This study provides new insights into the synthesis of efficient carbon-based catalysts for phenol degradation and water remediation. Full article

The development of ternary metal oxide electrocatalysts with optimized electronic structures and surface morphologies has emerged as one of the effective strategies to improve the performance of electrochemical water splitting. In this work, ternary CoMoCe (CMC)-oxide electrocatalysts were successfully synthesized on nickel foam substrates via a hydrothermal technique and employed for their catalytic activity in an alkaline electrolyte. For comparison, binary counterparts (CoMo, CoCe, and MoCe) were also fabricated under similar conditions. The synthesized catalysts’ electrodes exhibited diverse surface architectures, including microporous-flake hybrids, ultrathin flakes, nanoneedle-assembled microspheres, and randomly oriented hexagonal structures. Among them, the ternary CoMoCe-oxide electrode exhibited outstanding bifunctional electrocatalytic activity, delivering low overpotentials of 124 mV for the hydrogen evolution reaction (HER) at −10 mA cm⁻², and 340 mV for the oxygen evolution reaction (OER) at 100 mA cm⁻², along with excellent durability. Furthermore, in full water-splitting configuration, the CMC||CMC and RuO₂||CMC electrolyzers required cell voltages of 1.69 V and 1.57 V, respectively, to reach a current density of 10 mA cm⁻². Remarkably, the CMC-based electrolyzer reached an industrially relevant current density of 1000 mA cm⁻² at a cell voltage of 2.18 V, maintaining excellent stability over 100 h of continuous operation. These findings underscore the impact of an optimized electronic structure and surface architecture on design strategies for high-performance ternary metal oxide electrocatalysts. Herein, a robust and straightforward approach is comprehensively presented for fabricating highly efficient ternary metal-oxide catalyst electrodes, offering significant potential for scalable water splitting. Full article

Hybrid siloxane/silsesquioxane materials containing sterically demanding aromatic groups synthesized by hydrolysis and condensation suffer from incomplete cross-linking after thermal consolidation, limiting their thermal and mechanical performance. In this study, we systematically investigated a post-cross-linking strategy using various additives to enhance structural integrity and thermal stability. These include dimethyldimethoxysilane (DMDMS), diphenyldimethoxysilane (DPDMS) and phenyltrimethoxysilane (PTMS), as well as the organotin condensation catalyst di-n-butyltin diacetate (DBTA). Notably, we achieved thermal stability up to 453 °C and long-term transparency (up to 99%) at 200 °C with only little yellowing. Dynamic mechanical analysis demonstrated that post-cross-linking of precondensed siloxanes with PTMS, DPDMS, and DBTA enabled the formation of elastic materials exhibiting a rubbery plateau up to 200 °C. This behavior reflects enhanced structural rigidity and elasticity, which are essential for high-temperature applications. Our results show that high-temperature stability in siloxane/silsesquioxane materials is strongly influenced by factors such as the number of phenyl groups, cross-linking density, structural regularity, and degree of condensation. Most notably, the complete incorporation of a sterically demanding naphthyl-functionalized monomer during consolidation proved to be critical. Post-cross-linking significantly enhances all these parameters, which is essential for achieving robust thermal performance. Full article

Nickel-based metal–organic frameworks (Ni-MOFs) have received enormous amounts of attention from the scientific community due to their excellent porosity, larger specific surface area, tunable structure, and intrinsic redox properties. In previous years, Ni-MOFs and their hybrid composite materials have been extensively explored for electrochemical sensing applications. As per the reported literature, Ni-MOF-based hybrid materials have been used in the fabrication of electrochemical sensors for the monitoring of ascorbic acid, glucose, L-tryptophan, bisphenol A, carbendazim, catechol, hydroquinone, 4-chlorophenol, uric acid, kaempferol, adenine, _L-cysteine, etc. The presence of synergistic effects in Ni-MOF-based hybrid materials plays a crucial role in the development of highly selective electrochemical sensors. Thus, Ni-MOF-based materials exhibited enhanced sensitivity and selectivity with reasonable real sample recovery, which suggested their potential for practical applications. In addition, Ni-MOF-based hybrid composites were also adopted as electrode modifiers for the development of supercapacitors. The Ni-MOF-based materials demonstrated excellent specific capacitance at low current densities with reasonable cyclic stability. This review article provides an overview of recent advancements in the utilization of Ni-MOF-based electrode modifiers with metal oxides, carbon-based materials, MXenes, polymers, and LDH, etc., for the electrochemical detection of environmental pollutants and biomolecules and for supercapacitor applications. In addition, Ni-based bimetallic and trimetallic catalysts and their composites have been reviewed for electrochemical sensing and supercapacitor applications. The key challenges, limitations, and future perspectives of Ni-MOF-based materials are discussed. We believe that the present review article may be beneficial for the scientific community working on the development of Ni-MOF-based materials for electrochemical sensing and supercapacitor applications. Full article

Environmental pollution driven by socioeconomic development has intensified the need for advanced and sustainable wastewater treatment technologies. Herein, TiO₂-based photocatalysis emerged as a promising solution due to its oxidative potential, chemical stability, and eco-friendliness but does have unavoidable immobilized recoverability challenges. Therefore, this study explored the challenges and prospects of TiO₂-based photocatalysis for the degradation of emerging contaminants in wastewater. A comprehensive keyword analysis was conducted by using a decade of publications retrieved from Google Scholar, Scopus, and Web of Science (WOS) databases via Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) framework. From a pool of 518 refined publications, 318 significant keyword occurrences related to TiO₂-based photocatalysis advanced oxidation processes (AOPs) were revealed. The review delved into various types of AOP mechanisms and catalysts and highlighted the synergistic effect of process parameters and magnetization as recoverability potential for TiO₂-based photocatalysts. Furthermore, emerging strategies including surface modifications, doping, and hybrid AOP integrations were discussed to improve photocatalysis performance and industrial scalability. The study underscores the economic opportunity and environmental sustainability of degrading persistent organic pollutants by integrating a TiO₂-based photocatalytic system with a regenerative magnetic field into the water sector. Full article

Industrial processes like farming, food processing, petroleum refinery, and leather manufacturing produce a lot of high-salinity wastewater. This wastewater presents serious environmental risks, such as soil degradation, eutrophication, and water salinization, if it is released without adequate treatment. The sources and features of high-salinity wastewater are outlined in this review, along with the main methods for removing organic pollutants, such as physicochemical, biological, and combined treatment approaches. Membrane separation, coagulation–flocculation, and advanced oxidation processes are the primary physicochemical techniques. Anaerobic and aerobic technologies are the two categories into which biological treatments fall. Physicochemical–biological combinations and the fusion of several physicochemical techniques are examples of integrated technologies. In order to achieve sustainable and effective treatment and resource recovery of high-salinity wastewater, this review compares the effectiveness and drawbacks of each method and recommends that future research concentrate on the development of salt-tolerant catalysts, anti-fouling membrane materials, halophilic microbial consortia, and optimized hybrid treatment systems. Full article