Search Results (2,050)

In this explorative work, molybdenum trioxide (MoO₃) and representative doped MoO₃ materials, i.e., Cu-doped MoO₃ (2% Cu, “Cu-MoO₃”) and H-doped MoO₃ (H_0.31MoO₃, “H-MoO₃”), have been tested for the first time as photocatalysts in the UV-vis light-driven depolymerization of lignin. The catalysts have been characterized by XRD, TEM, ATR-FTIR, and UV-vis DRS. Under the adopted conditions (UV-vis irradiation, solvent 0.01 M aqueous NaOH, lignin 200 ppm, catalyst 1 g/L, rt, 5 h), photocatalytic depolymerization of wheat-straw lignin (WSL) produced increasing amounts of bio-oil on changing the catalyst from pristine MoO₃ to Cu-MoO₃ and H-MoO₃ (23%, 28% and 30%, respectively). Also, quantification of vanillin and vanillic acid shows a similar increasing trend. These results appear in line with the estimated band gap energies, which decrease in the order: MoO₃ (2.91 eV) > Cu-MoO₃ (2.86 eV) > H-MoO₃ (2.77 eV). H-MoO₃ shows the best catalytic performance, which was then fruitfully explored in the photocatalytic depolymerization of benchmark commercial Kraft lignin (bio-oil yield 32%, vanillin and vanillic acid yields 1.28% and 0.78%, respectively). In view of the results obtained, this work is expected to provide new ideas for the design of heterogeneous photocatalytic system for lignin cleavage. Full article

The synthesis, in particular the industrial production, of pharmaceuticals requires a broad arsenal of synthetic reactions capable of selectively forming specific structural motifs and assembling smaller building blocks into complex molecules. The Chan–Evans–Lam cross-coupling reaction, which forms a bond between a N-nucleophile and an aryl group from a boronic acid, catalysed by copper salts, is a typical example of this synthetic route. Considering the toxicity of copper and the stringent regulatory limits for its residues in final pharmaceutical products, a heterogeneous catalytic approach offers a viable alternative for this transformation. In this work, we present a simply and reproducibly synthesized catalyst based on copper nanoparticles supported on reduced graphene oxide (Cu-rGO), with high efficiency in a model Chan–Lam reaction involving benzimidazole and aniline derivatives with substituted boronic acids. Full article

Urban resilience has emerged as a critical paradigm for addressing the intertwined challenges of climate change, rapid urbanization, and social inequality, positioning green public spaces as catalysts for social, ecological, and institutional transformation. This article presents a systematic review conducted under the PRISMA 2020 guidelines, examining how collaborative and community participation influenced transformative urban resilience in green public spaces between 2021 and 2025. A total of 6179 records were initially identified across ScienceDirect and MDPI (last search: July 2025), of which 26 empirical studies met the inclusion criteria (peer-reviewed, empirical, published 2021–2025). Methodological rigor was strengthened through the application of the Mixed Methods Appraisal Tool (MMAT, 2018) and confidence in qualitative evidence was assessed using the GRADE-CERQual approach, enhancing transparency and reliability. Data extraction and synthesis followed a theoretical-methodological coding framework, allowing for the comparison of participatory strategies, typologies of green spaces, resilience dimensions, and applied instruments. The results show that multi-actor co-management, co-design, and community self-organization are the most frequent participatory strategies, while urban green infrastructure, pocket parks, and urban gardens constitute the predominant spatial contexts. Socio-ecological and social-participatory resilience emerged as dominant theoretical perspectives, with qualitative and mixed-methods designs prevailing across studies. Evidence synthesis through GRADE-CERQual identified seven key pathways—multi-actor co-management, Nature-based Solutions, community-based actions, social equity, cultural identity, institutional innovation, and planned densification—each contributing differently to resilience dimensions. Overall, the findings highlight that transformative resilience depends on deep, inclusive participatory processes, multi-level governance, and the integration of social, ecological, and cultural dimensions. Despite the heterogeneity of designs and unequal data adequacy, this review confirms that transformative urban resilience is a co-produced process grounded in community action, ecological sustainability, and collaborative governance. Strengthening underexplored areas—technological innovation, cultural resilience, and standardized methodological instruments—is essential for advancing comparative research and practice. Full article

Biodiesel, which is a blend of fatty acid methyl esters (FAME), has garnered significant attention as a promising alternative to petroleum-based diesel fuel. Nevertheless, the commercial production of biodiesel faces challenges due to the high costs associated with feedstock and the non-recyclable homogeneous catalyst system. To address these issues, a solid catalyst derived from construction industry waste cement was synthesized and utilized for biodiesel production from waste cooking oil (WCO). The catalyst’s surface and physical characteristics were analyzed through various techniques, including Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier Transform Infrared Spectroscopy (FTIR). The waste-cement catalyst demonstrated remarkable catalytic performance and reusability in the transesterification of WCO with methanol for biodiesel synthesis. A maximum biodiesel yield of 98.1% was obtained under the optimal reaction conditions of reaction temperature 65 °C; methanol/WCO molar ratio 16:1; calcined cement dosage 3 g; and reaction time 8 h. The apparent activation energy (Ea) from the reaction kinetic study is 35.78 KJ·mol⁻¹, suggesting that the transesterification reaction is governed by kinetic control rather than diffusion. The biodiesel produced exhibited high-quality properties and can be utilized in existing diesel engines without any modifications. This research presents a scalable, environmentally benign pathway for WCO transesterification, thereby contributing significantly to the economic viability and long-term sustainability of the global biodiesel industry. Full article

The Electro-Fenton (EF) process is a promising technology for the sustainable remediation of organic contaminants in complex wastewater. In this study, a weak magnetic field (~150 G) was applied to enhance the performance of an EF system using magnetite (Fe₃O₄) synthesized by a controlled co-precipitation route as a recyclable solid iron source. The magnetite was characterized by FTIR, SEM/EDS, and XPS, confirming the coexistence of Fe²⁺/Fe³⁺ species essential for in situ Fenton-like reactions. Under the selected operating conditions (90 min reaction time), magnetic-field assistance improved methylene blue decolorization from 14.2% to 46.0% at pH 3. FeSO₄ was used only as a homogeneous benchmark, whereas the magnetite-based system operated without soluble iron addition, minimizing sludge formation and secondary contamination. These results demonstrate the potential of magnetite-assisted and magnetically enhanced EF systems as a low-cost, sustainable alternative for the treatment of dye-containing industrial wastewater and other complex effluents. Full article

Ni-based catalysts have been extensively investigated for lignin hydrogenation; however, they often exhibit limited phenol selectivity and poor catalytic stability. To address these challenges, we introduced Cu as a promoter, resulting in the development of NiCu/ZSM-5 catalysts with significantly enhanced phenol selectivity and durability. Characterization studies revealed that Cu species form an alloy structure with Ni, which effectively suppresses the sintering of Ni nanoparticles during the catalytic process, thereby maintaining consistent performance over multiple reaction cycles. Furthermore, the Cu-Ni alloy demonstrated improved hydrogen activation capability while reducing overall H₂ uptake, leading to a marked increase in phenol selectivity compared to the Cu-free Ni/ZSM-5 catalyst. As a result, the Ni₁Cu₁/ZSM-5 (Ni/Cu molar ratio = 1:1) catalyst achieved a lignin conversion of 69.8% and a phenol selectivity of 84.4%, with negligible performance degradation over 8 cycles. The strategy presented in this work may offer an effective approach for enhancing the performance of industrial catalysts in lignin upgrading processes. Full article

Rural areas are currently facing a deepening “social-ecological divide,” where the fragmentation of natural, economic, and cultural data—often trapped in “data silos”—hinders effective systemic governance. To bridge this gap, in this study, the Rural Landscape Information Model (RLIM), an integrative framework designed to reconfigure rural connections through data fusion, process coordination, and performance feedback, is proposed. We validate the framework’s effectiveness through a comparative analysis of two distinct rural archetypes in China: the innovation-driven Yu Village and the heritage-conservation-oriented Hani Terraces. Our results reveal that digital technologies drive distinct empowerment pathways moderated by regional contexts: (1) In the data domain, heterogeneous resources were successfully integrated into the framework in both cases (achieving a Monitoring Coverage > 80%), yet served divergent strategic ends—comprehensive territorial management in Yu Village versus precision heritage monitoring in the Hani Terraces. (2) In the process domain, digital platforms restructured social interactions differently. Yu Village achieved high individual participation (Participation Rate ≈ 0.85) via mobile governance apps, whereas the Hani Terraces relied on cooperative-mediated engagement to bridge the digital divide for elderly farmers. (3) In the performance domain, the interventions yielded contrasting but positive economic-ecological outcomes. Yu Village realized a 25% growth in tourism revenue through “industrial transformation” (Ecology+), while the Hani Terraces achieved a 12% value enhancement by stabilizing traditional agricultural ecosystems (Culture+). This study contributes a verifiable theoretical model and a set of operational tools, demonstrating that digital technologies are not merely instrumental add-ons but catalysts for fostering resilient, collaborative, and context-specific rural socio-ecological systems, ultimately offering scalable governance strategies for sustainable rural revitalization in the digital era. Full article

The escalating global water crisis demands the development of cost-effective and environmentally sustainable treatment technologies. Among various advanced oxidation processes (AOPs), peracetic acid (PAA) has emerged as a promising oxidant, owing to its high redox potential, chemical stability, and potent disinfection capability. Nevertheless, the lack of highly efficient catalysts remains a major obstacle to achieving the effective degradation of contaminants of emerging concern in wastewater. Heterogeneous catalysis has proven to be a viable strategy for enhancing PAA activation, highlighting the urgent need for catalysts with superior activity, stability, and recyclability. Metal–organic frameworks (MOFs), with their large surface areas, tunable porosity, and structural diversity, provide versatile platforms for catalyst design. Recently, MOF-derived materials have attracted increasing attention for PAA activation, offering a new frontier in advanced oxidation technologies for efficient and sustainable wastewater remediation. This review systematically examines the role of MOFs in PAA activation, from pristine frameworks to MOF-based composites and MOF-derived catalysts. Mechanistic insights into PAA activation are highlighted, strategies for engineering MOF-based composites with synergistic catalytic properties are discussed, and the transformation of MOFs into robust derivatives with improved stability and reactivity is explored. Special attention is given to the identification and quantification of reactive species generated in PAA systems, providing a critical understanding of reaction pathways and catalytic performance. Finally, current challenges and future directions are outlined for designing highly efficient, recyclable, and environmentally compatible MOF-based catalysts, emphasizing their potential to significantly advance PAA-based AOPs. Full article

UiO-67(Zr), as a member of Zr-based metal–organic frameworks (MOFs), has attracted much attention owing to its merits, involving large surface area, high pore volume, and good structural stability. However, it is generally inactive in many catalytic reactions due to a lack of active sites. In this work, we report a new strategy, combining vapor-assisted synthesis with acid treatment to create abundant active sites in UiO-67(Zr), resulting from defects. The effects of some synthetic parameters were systematically investigated. As a result, an optimized material named UiO-67(Zr)-V-0.5FA-H, obtained by acid-treating UiO-67(Zr) and prepared with the addition of 0.5 mL formic acid via a vapor-assisted method, exhibited outstanding catalytic performance in the oxidation of dibenzothiophene (DBT), which can completely oxidize DBT in 9 min at 30 °C using H₂O₂ as the oxidant. The calculated turnover frequency reached 150.4 h⁻¹, surpassing those of most reported Zr-MOFs catalysts. In addition, it is demonstrated that UiO-67(Zr)-V-0.5FA-H is a heterogeneous catalyst and can be reused without obvious activity loss. Full article

The development of sustainable catalysts is the main objective in green chemistry approaches. In this study, a catalytically active polymer based on a tertiary amine was synthesized, functionalized with a photo-crosslinker, and structured into nanofibers via electrospinning technique with polycaprolactone (PCL) as a stabilizing additive. Subsequent photo-crosslinking yielded hierarchically porous polymers with high swelling properties and increased surface areas, thereby improving the accessibility of the immobilized catalytically active sites. The nanofiber mats were incorporated into a microfluidic reactor (MFR) setup and utilized as heterogeneous catalysts for the Knoevenagel reaction of malononitrile with different aldehydes. It was observed that the system demonstrated a substantial improvement in NMR yields (40–60%) and turnover frequencies (50–80 h⁻¹) in comparison to catalytical systems that had been previously published. Reusability studies showed reproducibility of NMR yields over up to three cycles. The obtained results demonstrate the potential of electrospun, photo-crosslinked nanofibers as efficient heterogeneous catalysts in microfluidic synthesis, thus contributing to more sustainable production of valuable malononitrile derivatives. Full article

Plastic streams dominated by polyethylene (PE) including PE HD/MD (High Density/Medium Density) and PE LD/LLD (Low Density/Linear Low Density), polypropylene (PP), and polyvinyl chloride (PVC) across Europe demand a design framework that links synthesis with end of life reactivity, supporting circular economic goals and European Union waste management targets. This work integrates polymerization derived chain architecture and depolymerization mechanisms to guide selective valorization of commercial plastic wastes in the European context. Catalytic topologies such as Bronsted or Lewis acidity, framework aluminum siting, micro and mesoporosity, initiators, and strategies for process termination are evaluated under relevant variables including temperature, heating rate, vapor residence time, and pressure as encountered in industrial practice throughout Europe. The analysis demonstrates that polymer chain architecture constrains reaction pathways and attainable product profiles, while additives, catalyst residues, and contaminants in real waste streams can shift radical populations and observed selectivity under otherwise similar operating windows. For example, strong Bronsted acidity and shape selective micropores favor the formation of C₂ to C₄ olefins and Benzene, Toluene, and Xylene (BTX) aromatics, while weaker acidity and hierarchical porosity help preserve chain length, resulting in paraffinic oils and waxes. Increasing mesopore content shortens contact times and limits undesired secondary cracking. The use of suitable initiators lowers the energy threshold and broadens processing options, whereas diffusion management and surface passivation help reduce catalyst deactivation. In the case of PVC, continuous hydrogen chloride removal and the use of basic or redox co catalysts or ionic liquids reduce the dehydrochlorination temperature and improve fraction purity. Staged dechlorination followed by subsequent residue cracking is essential to obtain high quality output and prevent the release of harmful by products within European Union approved processes. Framing process design as a sequence that connects chain architecture, degradation chemistry, and operating windows supports mechanistically informed selection of catalysts, severity, and residence time, while recognizing that reported selectivity varies strongly with reactor configuration and feed heterogeneity and that focused comparative studies are required to validate quantitative structure to selectivity links. In European post consumer sorting chains, PS and PC are frequently handled as separate fractions or appear in residues with distinct processing routes, therefore they are not included in the polymer set analyzed here. Polystyrene and polycarbonate are outside the scope of this review because they are commonly handled as separate fractions and are typically optimized toward different product slates than the gas, oil, and wax focused pathways emphasized here. Full article

The deployment of solar and other renewable energy technologies (RETs) plays a central role in the global energy transition and the pursuit of sustainable development. Beyond reducing greenhouse gas emissions, these technologies generate far-reaching societal co-benefits that shape environmental quality, social equity, and economic growth. This study systematically reviews peer-reviewed literature published between 2009 and 2025 to identify, integrate, and assess empirical evidence on how RET deployment contributes to societal welfare. Following the SALSA framework and PRISMA guidelines, 147 studies were selected from Scopus and Web of Science. The evidence reveals a consistent welfare triad: environmental gains (emission and pollution reduction, climate mitigation), social gains (improved health, affordability, energy security, and inclusion), and economic gains (employment and income growth, local development). These benefits are, however, heterogeneous and depend on enabling conditions such as policy stability, financial development, grid integration, innovation capacity, and social acceptance. The review highlights that solar energy, in particular, acts as both an environmental and social catalyst in advancing sustainable welfare outcomes. The findings provide a comprehensive basis for policymakers and researchers seeking to design equitable and welfare-enhancing renewable energy transitions. Full article

The development of sustainable catalysts from renewable resources is a key challenge for reducing the cost of industrial catalytic processes and waste valorization. In this work, low-cost heterogeneous active catalysts were prepared based on pyrolyzed forest residues, forming valuable porous support materials (Biochar) able to efficiently accommodate the highly active heteropolyacid HPW₁₂. Further, magnetic functionality was incorporated in the novel catalytic materials by the impregnation of NiFe₂O₄. The resulting magnetic composites were characterized by FTIR-ATR, SEM-EDS, ICP-OES, BET, XRD, potentiometric titration and magnetometry. The novel HPW₁₂@NiFe₂O₄@Biochar composites were able to valorize the glycerol to produce the fuel additive solketal with high conversion and high selectivity after only 3 h of reaction via acetalization reaction with acetone. The biochar catalytic composite prepared from cork presented higher pore size than the same prepared from forest biomass. This property was crucial to achieve the best conversion (89%) and the highest solketal selectivity (96%). Additionally, reusability capacity was verified, supporting the potential of the cork-pyrolyzed-based composites as potential low-cost catalytic material to produce fuel additives, such as solketal, under sustainable conditions. This may contribute one step further toward a future with greener energy, increasing the viability of biodiesel industry waste. Full article

Photo-Fenton advanced oxidation processes are promising and sustainable approaches for water treatment, particularly under visible-light irradiation. In this study, Cu-Fe bimetallic catalysts supported on silica and γ-alumina were developed for visible-light-driven photo-Fenton reactions, with emphasis on the influence of metal ratios and support-metal interactions on charge–carrier dynamics and hydroxyl radical formation. Comprehensive characterization (XRD, TEM, UV-Vis DRS, PL, TCSPC, and EPR) revealed stronger metal–support interactions and higher metal dispersion on γ-alumina, while silica-supported catalysts showed CuO aggregation at higher Cu loadings. Catalytic performance was evaluated using coumarin oxidation as both a model reaction and a quantitative probe for ^•OH radical generation. Alumina-supported catalysts exhibited superior activity, and ^•OH production increased with increasing Cu content on both supports. Importantly, iron was found to play a dual role: low Fe loading enhances photo-Fenton activity, whereas higher Fe content promotes charge–carrier recombination, leading to reduced activity under visible-light irradiation. These results highlight how the interplay between Fe/Cu ratio and support material governs charge dynamics and provides clear guidelines for the rational design of efficient heterogeneous photo-Fenton catalysts. Full article