Search Results (663)

With the increasing emphasis on environmental protection and sustainable development, improving air pollution control technology has become imperative. In this study, Ce-based catalysts are used as research objects to explore the effects of hydrothermal aging on their performance in oxidizing PM. Different Mn, Na, Pt and Zr-doped Ce-based catalysts were prepared based on the impregnation method and the PM oxidation performance of Ce-based catalysts before and after hydrothermal aging was investigated using thermogravimetric experiments, and the catalytic activity change pattern of fresh/hydrothermal aging Ce-based catalysts was analyzed by comparing the comprehensive combustion index S and combustion stability index Rw, revealing the PM oxidation process. The conclusion showed that the cerium-based catalyst significantly enhanced the oxidation efficiency of PM compared with PU. By comparing the performance of different metal-modified catalysts, it was found that the order of activity was: Pt > Na > Mn > Zr. With the metal doping increased, only the comprehensive combustion index S and combustion stability index Rw of Na/CeO₂ catalysts decreased. After hydrothermal aging treatment, the Zr/CeO₂ catalysts showed the best hydrothermal aging resistance, and the comprehensive combustion index S and combustion stability index Rw remained stable (<5%). Ce-based catalysts have the strongest to weakest hydrothermal aging resistance in the following order: Zr > Mn > Pt > Na. This study not only provides an important scientific reference for the application of Ce-based catalysts in the field of environmental purification but also contributes new ideas and methods to promote the green and sustainable development of air pollution control technology. Full article

The production of fuels and materials from residual biomass through sustainable processes is one of the most challenging goals for science and technology. Such development is highly ambitious because of the complex composition of the feedstock (lipidic and lignocellulosic). To succeed, biomass conversion technologies must be able to compete economically with technologies based on fossil carbon. The use of specific and more available catalysts combined with improved reaction conditions can significantly reduce overall industrial costs and maximize efficiency. The synthesis and application of optimized catalytic systems are essential to modulate their activity, ensuring at the same time a high resistance to deactivation. For this reason, the study of multifunctional systems is gaining increasing interest alongside new industrial technologies. Here, we review significant recent advances in sustainable catalytic biomass conversion using emerging heterogeneous catalysts. Full article

As water pollution from dyes, pharmaceuticals, heavy metals, and other emerging contaminants continues to rise at an alarming rate, ensuring access to clean and safe water has become a pressing global challenge. Conventional water treatment methods, though widely used, often fall short in effectively addressing these complex pollutants. In response, researchers have turned to Advanced Functional Membranes (AFMs) as promising alternatives, owing to their customizable structures and enhanced performance. Among the most explored AFMs are those based on metal–organic frameworks (MOFs), carbon nanotubes (CNTs), and electro–catalytic systems, each offering unique advantages such as high permeability, selective pollutant removal, and compatibility with advanced oxidation processes (AOPs). Notably, hybrid systems combining AFMs with electrochemical or photocatalytic technologies have demonstrated remarkable efficiency in laboratory settings. However, translating these successes to real-world applications remains a challenge due to issues related to cost, scalability, and long-term stability. This review explores the recent progress in AFM development, particularly MOF-based, CNT-based, and electro-Fenton (EF)-based membranes, highlighting their material aspects, pollutant filtration mechanisms, benefits, and limitations. It also offers insights into how these next-generation materials can contribute to more sustainable, practical, and economically viable water purification solutions in the near future. Full article

In this study, the use of spent coffee waste as a green precursor of polyphenolic compounds, which are subsequently employed as reducing agents for the synthesis of zero-valent iron nanoparticles (nZVI) aimed at the efficient removal of dyes from aqueous systems, has been investigated. The nanoparticles, generated in situ in the presence of controlled amounts of hydrogen peroxide, were applied in the removal of organic dyes—including methylene blue, methyl orange, and orange G—through a heterogeneous Fenton-like catalytic process. The synthesized nZVI were thoroughly characterized by nitrogen adsorption at 77 K, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), and powder X-ray diffraction (XRD). A statistical design of experiments and response surface methodology were employed to evaluate the effect of polyphenol, Fe(III), and H₂O₂ concentrations on dye removal efficiency. Results showed that under optimized conditions, a 100% removal efficiency could be achieved. This work highlights the potential of nZVI synthesized from agro-industrial waste through sustainable routes as an effective solution for water remediation, contributing to circular economy strategies and environmental protection. Full article

The global transition toward renewable energy sources has intensified in response to escalating environmental challenges. Nevertheless, the inherent intermittency and instability of renewable energy necessitate the development of reliable energy storage technologies. Supercapacitors are particularly notable for their high specific capacitance, rapid charge and discharge capability, and exceptional cycling stability. Concurrently, the increasing demand for efficient and sustainable energy storage systems has stimulated interest in multifunctional electrode materials that integrate electrocatalytic activity with electrochemical energy storage. Two-dimensional transition metal dichalcogenides (TMDs), owing to their distinctive layered structures, large surface areas, phase state, energy band structure, and intrinsic electrocatalytic properties, have emerged as promising candidates to achieve dual functionality in electrocatalysis and electrochemical energy storage for asymmetric supercapacitors (ASCs). Specifically, their unique electronic properties and catalytic characteristics promote reversible Faradaic reactions and accelerate charge transfer kinetics, thus markedly enhancing charge storage efficiency and energy density. This review highlights recent advances in TMD-based multifunctional electrodes. It elucidates mechanistic correlations between intrinsic electronic properties and electrocatalytic reactions that influence charge storage processes, guiding the rational design of high-performance ASC systems. Full article

Thermo-catalytic decomposition (TCD) presents a promising pathway for producing hydrogen from natural gas without emitting CO₂. This process represents a form of fossil fuel decarbonization where the byproduct, rather than being a greenhouse gas, is a solid carbon material with potential for commercial value. This study examines the dynamic behavior of TCD, showing that carbon formed during the reaction first enhances and later dominates methane decomposition. Three types of carbon materials were employed as starting catalysts. Methane decomposition was continuously monitored using on-line Fourier transform infrared (FT-IR) spectroscopy. The concentration and nature of surface-active sites were determined using a two-step approach: oxygen chemisorption followed by elemental analysis through X-ray photoelectron spectroscopy (XPS). Changes in the morphology and nanostructure of the carbon catalysts, both before and after TCD, were examined using high-resolution transmission electron microscopy (HRTEM). Thermogravimetric analysis (TGA) was used to study the reactivity of the TCD deposits in relation to the initial catalysts. Partial oxidation altered the structural and surface chemistry of the initial carbon catalysts, resulting in activation energies of 69.7–136.7 kJ/mol for methane. The presence of C₂ and C₃ species doubled methane decomposition (12% → 24%). TCD carbon displayed higher reactivity than the nascent catalysts and sustained long-term activity. Full article

Nitrile-containing compounds are integral to pharmaceuticals, agrochemicals and polymer industries, yet their environmental persistence and toxicity pose major challenges. Biocatalytic approaches using nitrile-converting enzymes—particularly nitrilases and nitrile hydratases—offer sustainable alternatives to conventional hydrolysis, enabling the selective transformation of nitriles into amides and acids under mild conditions. This review presents an industrial perspective on nitrile-converting enzymes, summarising their catalytic potential, current limitations, and emerging strategies for stability, activity and performance enhancement. Advances in protein engineering, metagenomic discovery and biocatalytic optimisation have already expanded their wider applicability, while synthetic biology and protein design tools are accelerating the development of tailored biocatalysts. The integration of these enzymes into cascades and chemoenzymatic processes supports scalable and innovative solutions to green manufacturing. Collectively, these emerging strategies position nitrile-converting enzymes as versatile tools for sustainable catalysis, with growing relevance in fine chemical synthesis, waste remediation, and bio-based synthetic platforms. 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 work, the removal of Cu(II) ions from an aqueous effluent was studied using an Mg/Fe layered double hydroxide (LDH) as the adsorbent. The material was synthesized and characterized before and after the adsorption process to identify structural and morphological changes induced by copper uptake. Techniques such as X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), ultraviolet-visible spectroscopy (UV-Vis), Raman spectroscopy, and nitrogen physisorption (BET) were employed to confirm the interaction between the metal ions and the LDH surface. The LDH-Mg/Fe exhibited a high maximum adsorption capacity of 526 mg/g, and the adsorption kinetics followed a pseudo-second-order model, achieving over 90% removal of Cu(II) within 2.5 h. The Cu(II)-loaded material was subsequently evaluated as a sustainable catalyst in two applications: (i) an organic synthesis via “click” chemistry, reaching yields of up to 85%, and (ii) the decoloration of Congo Red via a Fenton-like process, achieving a decoloration efficiency of at least 84%. These dual uses demonstrate the potential of Cu(II)-loaded LDH as a cost-effective and environmentally friendly approach to simultaneous pollutant removal and catalytic valorization. Full article

Photocatalytic nitrogen fixation under ambient conditions offers a sustainable alternative to the energy-intensive Haber–Bosch process, yet remains limited by the inertness of N≡N bonds and sluggish multi-electron/proton transfer kinetics. Nature’s nitrogenase enzymes, featuring the FeMo cofactor and ATP-driven electron cascades, inspire a new generation of artificial systems capable of mimicking their catalytic precision and selectivity. This review systematically summarizes recent advances in bio-inspired photocatalytic nitrogen reduction, focusing on six key strategies derived from enzymatic mechanisms: Fe–Mo–S active site reconstruction, hierarchical electron relay pathways, ATP-mimicking energy modules, defect-induced microenvironments, interfacial charge modulation, and spatial confinement engineering. While notable progress has been made in enhancing activity and selectivity, challenges remain in dynamic regulation, mechanistic elucidation, and system-level integration. Future efforts should prioritize operando characterization, adaptive interface design, and device-compatible catalyst platforms. By abstracting nature’s catalytic logic into synthetic architectures, biomimetic photocatalysis holds great promise for scalable, green ammonia production aligned with global decarbonization goals. Full article

The ethanol oxidation reaction (EOR) is a key process for direct ethanol fuel cells (DEFCs), offering a high-energy-density and carbon-neutral pathway for sustainable energy conversion. However, the practical implementation of DEFCs is significantly hindered by the EOR due to its sluggish kinetics, complex multi-electron transfer pathways, and severe catalyst poisoning by carbonaceous intermediates. This review provides a comprehensive and mechanistically grounded overview of recent advances in EOR electrocatalysts, with a particular emphasis on the structure–activity relationships of noble metals (Pt, Pd, Rh, Au) and non-noble metals. The effects of catalyst composition, surface structure, and electronic configuration on C–C bond cleavage efficiency, product selectivity (C1 vs. C2), and CO tolerance are critically evaluated. Special attention is given to the mechanistic distinctions among different metal systems, highlighting how these factors influence reaction pathways and catalytic behavior. Key performance-enhancing strategies—including alloying, nanostructuring, surface defect engineering, and support interactions—are systematically discussed, with mechanistic insights supported by in situ characterization and theoretical modeling. Finally, this review identifies major challenges and emerging opportunities, outlining rational design principles for next-generation EOR catalysts that integrate high activity, durability, and scalability for real-world DEFC applications. Full article

Laccases, a class of multicopper oxidases found in diverse biological sources, have emerged as key green biocatalysts with significant potential for eco-friendly pollutant degradation. Their ability to drive electron transfer reactions using oxygen, converting pollutants into less harmful products, positions laccases as promising tools for scalable and sustainable treatment of wastewater, soil, and air pollution. This review explores laccase from a translational perspective, tracing its journey from laboratory discovery to real-world applications. Emphasis is placed on recent advances in production optimization, immobilization strategies, and nanotechnology-enabled enhancements that have improved enzyme stability, reusability, and catalytic efficiency under complex field conditions. Applications are critically discussed for both traditional pollutants such as synthetic dyes, phenolics, and pesticides and emerging contaminants, including endocrine-disrupting chemicals, pharmaceuticals, personal care products, microplastic additives, and PFAS. Special attention is given to hybrid systems integrating laccase with advanced oxidation processes, bioelectrochemical systems, and renewable energy-driven reactors to achieve near-complete pollutant mineralization. Challenges such as cost–benefit limitations, limited substrate range without mediators, and regulatory hurdles are evaluated alongside solutions including protein engineering, mediator-free laccase variants, and continuous-flow bioreactors. By consolidating recent mechanistic insights, this study underscores the translational pathways of laccase, highlighting its potential as a cornerstone of next-generation, scalable, and eco-friendly remediation technologies aligned with circular bioeconomy and low-carbon initiatives. Full article

Achieving ultra-low-sulfur diesel is a crucial objective in modern fuel refining, driven by increasingly stringent environmental regulations. This study presents the development of a highly efficient oxidative–adsorptive desulfurization process utilizing a nanocatalyst synthesized from biowaste eggshell-extracted calcite. The oxidation reaction was conducted in a digital basket reactor (DBR), an advanced reactor system designed to enhance mass transfer and catalytic efficiency. To further augment the catalyst’s performance, the calcite was modified with eco-friendly MnO₂, while activated carbon was employed as an adsorbent to effectively capture oxidized sulfur compounds, ensuring compliance with ultra-low-sulfur fuel standards. The synthesized nanocatalyst underwent comprehensive physicochemical characterization using SEM, EDX, BET, and FTIR, confirming its high surface area, structural integrity, and superior catalytic activity. The MnO₂/P–calcite catalyst achieved a sulfur removal efficiency of 96.5% at 90 °C, 80 min, and 600 rpm, demonstrating excellent oxidative–adsorptive performance for real diesel fuel. The integration of this innovative nanocatalyst with the DBR system presents a sustainable, cost-effective, and industrially viable approach for deep desulfurization, offering significant advancements in clean fuel production and environmental sustainability. Full article

With the rapid industrialization, excessive reliance on fossil fuels has resulted in energy crises and environmental pollution, driving the search for sustainable alternatives. Biomass-derived resources have emerged as promising candidates to replace fossil-based feedstocks. Among these, furfural (FF) serves as a key platform molecule that can be catalytically hydrogenated to various high-value chemicals, with furfuryl alcohol (FA) representing one of the most valuable products. Currently, Cr-based catalysts remain predominant for the selective hydrogenation of FF to FA. However, the severe environmental toxicity of Cr necessitates urgent development of alternative Cr-free catalytic systems. This study systematically reviews recent advances in FF hydrogenation to FA, providing an in-depth discussion of reaction mechanisms, including adsorption configurations, solvent effects, and side reactions, as well as a comprehensive analysis of structure–activity relationships, involving active metal, support, promoter, and preparation methods. Furthermore, we evaluate the application of the advanced characterization techniques for monitoring the reaction processes. Finally, we propose the future research directions: (1) designing efficient and stable non-noble metal catalysts and (2) elucidating reaction mechanisms via the combined in situ characterization and theoretical calculations. These efforts would facilitate the academic understanding and industrial implementation of the FF-to-FA conversion process. Full article

The hydrogenation of p-cymene to p-menthane, a bio-based solvent, over four platinum-group catalysts, was thoroughly investigated in this study. The effect of the support material, pressure, and temperature were explored. Rhodium was the most effective metal, even under normal pressure conditions. Charcoal was a better metal support compared to alumina, offering better selectivity at lower pressure and outstanding recyclability. Hydrogen pressure had no effect on the selectivity; however, the conversion rate was maximal at higher pressure. At higher temperatures, the thermodynamically stable trans-isomer was favored, whereas at lower temperatures the cis-isomer became predominant. Remarkably, Rh/C achieved >99% conversion of p-cymene and maintained stable activity and selectivity over 66 recycling cycles, whereas the same metal-based catalyst on alumina was only recycled twice. These findings demonstrate that the solvent-free hydrogenation of p-cymene can be efficiently achieved using commercially available catalysts, with Rh/C emerging as a promising benchmark for sustainable and green catalytic processes. Full article