Search Results (40)

Progressive research on reducing engine emissions is highly valued due to the emissions’ significant environmental and health impacts. This comprehensive comparative study examines the catalytic efficiency of manganese (Mn) and cerium silica (Ce-Si) synthesis catalyst-based molds in a diesel engine using a selective catalytic reduction (SCR) technique with diesel and diesel–plastic oil blend (DPB) (B50). In addition to Fourier transform infrared spectroscopy (FTIR) studies, X-ray diffraction (XRD), scanning electron microscopy (SEM), and the Brunauer–Emmett–Teller (BET) method are utilized to characterize the produced molds before and after exhaust gas passes. The Ce-Si-based mold demonstrates superior redox capacity, better adsorption capacity, and better thermal stability, attributed to enhanced oxygen storage and structural integrity compared to the Mn-based mold. Under minimum load conditions, nitrogen oxide (NO) reduction efficiency peaks at 80.70% for the Ce-Si-based mold in the SCR treatment with DPB fuel. Additionally, significant reductions of 86.84%, 65.75%, and 88.88% in hydrocarbon (HC), carbon monoxide (CO), and smoke emissions, respectively, are achieved in the SCR treatment under optimized conditions. Despite a wide temperature range, Ce-Si-based mold promotes high surface area and superior gas diffusion properties. Overall, the Ce-Si-based mold provides efficient emission control in diesel engines, which paves a path for developing better environmental sustainability. The outcomes contribute to advancing environmental sustainability by supporting the achievement of SDGs 7, 11, and 13. Full article

Global municipal solid waste (~2B tons/year) affects sustainability, as landfill and incineration face persistent leachate contamination, demanding effective management to advance water recycling and circular economies. Accelerated investigation of hybrid biocatalytic ozonation systems is imperative to enhance contaminant removal efficiency for stringent discharge compliance. This study investigates the catalytic ozonation effects of γ-Al₂O₃-based catalysts loaded with different metals (Cu, Mn, Zn, Y, Ce, Fe, Mg) on the biochemical effluent of landfill leachate. The catalysts were synthesized via a mixed method and subsequently characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD). Pseudo-second-order kinetics revealed active metal loading’s impact on adsorption capacity, with Cu/γ-Al₂O₃ and Mg/γ-Al₂O₃ achieving the highest Q_e (0.85). To elucidate differential degradation performance among the catalysts, the ozone/oxygen gas mixture was introduced at a controlled flow rate. Experimental results demonstrate that the Cu/γ-Al₂O₃ catalyst, exhibiting optimal comprehensive degradation performance, achieved COD and TOC removal efficiencies of 84.5% and 70.9%, respectively. UV–vis absorbance ratios revealed the following catalytic disparities: Mg/γ-Al₂O₃ achieved the highest aromatic compound removal efficiency; Ce/γ-Al₂O₃ excelled in macromolecular organics degradation. EEM-PARAFAC analysis revealed differential fluorophore removal: Cu/γ-Al₂O₃ exhibited broad efficacy across all five components, while Mg/γ-Al₂O₃ demonstrated optimal removal of C2 and C4, but showed limited efficacy toward C5. These findings provide important insights into selecting catalysts in practical engineering applications for landfill leachate treatment. This study aims to elucidate catalyst formulation-dependent degradation disparities, guiding water quality-specific catalyst selection to ultimately enhance catalytic ozonation efficiency. Full article

Manganese-based oxides with good redox properties exhibit high soot oxidation activity. To further enhance their catalytic performance, introducing additional metal elements into manganese-based oxides is considered an effective approach. Herein, two rare earth elements (Sm and Ce)-modified MnO_x catalysts were prepared by the co-precipitation method. The synthesized MnO_x catalyst primarily consists of the Mn₃O₄ phase, with trace amounts of Mn₅O₈. The addition of Sm or Ce maintains the predominance of the Mn₃O₄ phase, increases the proportion of Mn₅O₈, and enhances the redox properties, thereby boosting the catalytic activity for NO and soot oxidation. Notably, the coexistence of Sm and Ce achieves optimal soot oxidation activity, with T₁₀ reaching 306 °C. Comprehensive physicochemical characterization elucidates the underlying structure–performance relationships of these catalysts. Full article

Cu-containing and Ce-modified OMS-2 catalysts were prepared at various calcination temperatures using the hydrothermal method and tested for low-temperature CO oxidation. The structure, chemical compositions, and physical–chemical properties of the catalysts were characterized using XRD, N₂ physisorption, XRF, Raman spectroscopy, SEM, high-resolution TEM with EDX, TPR-H₂, and XPS. The incorporation of Cu into the Ce-OMS-2 sample facilitated the transformation of pyrolusite into cryptomelane, as confirmed by Raman spectroscopy data. In the light-off mode, the Cu/Ce-OMS-2-300 and Cu/OMS-2 samples exhibited higher activity in low-temperature CO oxidation (T₉₀ = 115 and 121 °C, respectively) compared to sample Cu/Ce-OMS-2-450. After a long-run stability test, the Cu/Ce-OMS-X samples demonstrated excellent performance: the T₈₀ increased by 16% and 7% for the samples calcined at 300 °C and 450 °C, respectively, while the T₈₀ for the Cu/OMS-2 increased by 40%. The Cu/OMS-2 and Cu/Ce-OMS-2-300 samples were found to have an increased content of nanodispersed copper sites on their surfaces. These copper sites contributed to the formation of the Cu²⁺-O-Mn⁴⁺ interface, which is responsible for the CO oxidation. The presence of Ce³⁺ in the catalyst was found to increase its stability in the presence of water vapor due to the higher reoxidation ability in comparison with Ce-free sample Cu/OMS-2. Full article

The conversion of NO_x and the yield of N₂O during NH₃-SCR-DeNO_x below 473 K over TiO₂-supported transition metal oxide catalysts with equal loading of 20 wt.-% decreases in the following order of the supported oxides: MnO_x > CuO_x > CoO_x > FeO_x > NiO_x > CeO_x. The storage capacity for NH₃, characterized by the acid site density of the catalyst, is not directly correlated with the catalytic activity. Rather, the temperature range for the reduction of the supported transition metal oxides as determined by TPR-H₂ is the main governing factor for high NH₃-SCR-DeNO_x activity, especially in the temperature range below 473 K. At the same time, oxidation temperature range and the density of Lewis acid sites govern the formation of N₂O. The decomposition of NH₄NO₃ as an intermediate in the NH₃-SCR-DeNO_x reaction is determined by the redox property of TMO-based catalysts, which further influences both the windows of the decomposition temperature and the yield of N₂O. The correlation between the redox properties and the activity for NH₃-SCR-DeNO_x was confirmed for a series of MnO_x-CeO_x/TiO₂-SiO₂ mixed transition metal oxide catalysts as a promising combination of the less active and more selective CeO_x with less selective and highly active MnO_x. The linear correlation between reduction temperature range and the NH₃-SCR-DeNO_x activity indicates that the found relation can be transferred to other supported transition metal-containing catalysts for low-temperature NH₃-SCR-DeNO_x. Full article

The development and characterization of synthesis techniques for oxide materials based on ceria is a subject of extensive study with the objective of their wide-ranging applications in pursuit of sustainable development. The present study demonstrates the feasibility of controlled synthesis of Ce_1−xM_xO_2−δ (M = Fe, Ni, Co, Mn, Cu, Ag, Sm, Cs, x = 0.0–0.3) in combustion reactions from precursors comprising glycine, polyvinyl alcohol, polyvinylpyrrolidone, polyethylene glycol, and cellulose as organic components. Controlled synthesis is achieved by varying the composition of the precursor, the type of organic component, and the amount of organic component, which allows for the influence of the generation of high-density electrical charges and outgassing during synthesis. The intensity of charge generation is quantified by measuring the value of the precursor–ground potential difference. It has been demonstrated that an increase in the intensity of charge generation results in a more developed morphology, which is essential for the practical implementation of ceria as a catalyst to enhance contact with gases and solid particles. The maximum value of the potential difference, equal to 68 V, is obtained during the synthesis of Ce_0.7Ni_0.3O_2−δ with polyvinyl alcohol in stoichiometric relations, which corresponds to a specific surface area of 21.7 m² g⁻¹. A correlation is established between the intensity of gas release for systems with different organic components, the intensity of charge generation, morphology, and the value of the specific surface area of the samples. Full article

Ammonia is known as an alternative hydrogen supplier because of its high hydrogen content and convenient storage and transport. Hydrogen production from ammonia decomposition also provides a source of hydrogen for fuel cells. While catalysts composed of ruthenium metal atop various support materials have proven to be effective for ammonia decomposition, non-precious-metal-based catalysts are attracting more attention due to desires to reduce costs. We prepared a series of Fe, Co, Ni, Mn, and Cu monometallic catalysts and their alloys as catalysts over proton-conducting ceramics via the impregnation method as precious-metal-free ammonia decomposition catalysts. While Co and Ni showed superior performance compared to Fe, Mn, and Cu on a BaZr_0.1Ce_0.7Y_0.1Yb_0.1O_3−б (BZCYYb) support as an ammonia decomposition catalyst, the cost of Fe is much lower than that of other metals. Alloying Fe with Co can significantly increase the conversion and stability and lower the overall cost of materials. The measured ammonia decomposition rate of FeCo/BZCYYb reached 100% at 600 °C, and the ammonia decomposition rate was almost unchanged during the long-term test of 200 h, which reveals its good catalytic activity for ammonia decomposition and thermal stability. When the metallic catalyst remained unchanged, BZCYYb also exhibited better performance compared to other commonly used oxide supports. Finally, when ammonia cracked using our alloy catalyst was fed to solid oxide fuel cells (SOFCs), the peak power densities were very close to that achieved with a simulated fully cracked gas stream, i.e., 75% H₂ + 25% N₂, thus proving the effectiveness of this new type of ammonia decomposition catalyst. Full article

A series of M(x)CoCeMgAlO mixed oxides with different transition metals (M = Cu, Fe, Mn, and Ni) with an M content x = 3 at. %, and another series of Fe(x)CoCeMgAlO mixed oxides with Fe contents x ranging from 1 to 9 at. % with respect to cations, while keeping constant in both cases 40 at. % Co, 10 at. % Ce and Mg/Al atomic ratio of 3 were prepared via thermal decomposition at 750 °C in air of their corresponding layered double hydroxide (LDH) precursors obtained by coprecipitation. They were tested in a fixed bed reactor for complete methane oxidation with a gas feed of 1 vol.% methane in air to evaluate their catalytic performance. The physico-structural properties of the mixed oxide samples were investigated with several techniques, such as powder X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDX), elemental mappings, inductively coupled plasma optical emission spectroscopy (ICP-OES), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction under hydrogen (H₂-TPR) and nitrogen adsorption–desorption at −196 °C. XRD analysis revealed in all the samples the presence of Co₃O₄ crystallites together with periclase-like and CeO₂ phases, with no separate M-based oxide phase. All the cations were distributed homogeneously, as suggested by EDX measurements and elemental mappings of the samples. The metal contents, determined by EDX and ICP-OES, were in accordance with the theoretical values set for the catalysts’ preparation. The redox properties studied by H₂-TPR, along with the surface composition determined by XPS, provided information to elucidate the catalytic combustion properties of the studied mixed oxide materials. The methane combustion tests showed that all the M-promoted CoCeMgAlO mixed oxides were more active than the M-free counterpart, the highest promoting effect being observed for Fe as the doping transition metal. The Fe(x)CoCeMgAlO mixed oxide sample, with x = 3 at. % Fe displayed the highest catalytic activity for methane combustion with a temperature corresponding to 50% methane conversion, T₅₀, of 489 °C, which is ca. 40 °C lower than that of the unpromoted catalyst. This was attributed to its superior redox properties and lowest activation energy among the studied catalysts, likely due to a Fe–Co–Ce synergistic interaction. In addition, long-term tests of Fe(3)CoCeMgAlO mixed oxide were performed, showing good stability over 60 h on-stream. On the other hand, the addition of water vapors in the feed led to textural and structural changes in the Fe(3)CoCeMgAlO system, affecting its catalytic performance in methane complete oxidation. At the same time, the catalyst showed relatively good recovery of its catalytic activity as soon as the water vapors were removed from the feed. Full article

Herein, motivated by the excellent redox properties of rod-shaped ceria (CeO₂-NR), a series of TM/CeO₂ catalysts, employing the first-row 3d transition metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) as active metal phases, were comparatively assessed under identical synthesis and reaction conditions to decipher the role of active metal in the CO₂ hydrogenation process. Notably, a volcano-type dependence of CO₂ hydrogenation activity/selectivity was disclosed as a function of metal entity revealing a maximum for the Ni-based sample. Ni/CeO₂ is extremely active and fully selective to methane (Y_CH4 = 90.8% at 350 °C), followed by Co/CeO₂ (Y_CH4 = 45.2%), whereas the rest of the metals present an inferior performance. No straightforward relationship was disclosed between the CO₂ hydrogenation performance and the textural, structural, and redox properties, whereas, on the other hand, a volcano-shaped trend was established with the relative concentration of oxygen vacancies and partially reduced Ce³⁺ species. The observed trend is also perfectly aligned with the previously reported volcano-type dependence of atomic hydrogen adsorption energy and CO₂ activation as a function of 3d-orbital electron number, revealing the key role of intrinsic electronic features of each metal in conjunction to metal–support interactions. Full article

Pt supported on carbon (Pt/C) is deemed as the state-of-the-art catalyst towards oxygen reduction reactions (ORRs) in chemical and biological fuel cells. However, due to the high cost and scarcity of Pt, researchers have focused on the development of Earth-abundant non-precious metal catalysts, hoping to replace the traditional Pt/C catalyst and successfully commercialize the chemical and biological fuel cells. In this regard, electrocatalysts made of transition metals emerged as excellent candidates for ORRs, especially the electrocatalysts made of Fe and Co in combination with N-doped carbons, which produce potentially active M-N₄-C (M=Co, Fe) ORR sites. At present, however, the transition metal-based catalysts are popular; recently, electrocatalysts made of rare earth metals are emerging as efficient catalysts, due to the fact that rare earth metals also have the potential to form rare earth metal-N₄-C active sites, just like transition metal Fe-N₄-C/Co-N₄-C. In addition, mixed valance states and uniqueness of f-orbitals of the rare earth metals are believed to improve the redox properties of the catalyst that helps in enhancing ORR activity. Among the rare earth metals, Ce is the most interesting element that can be explored as an ORR electrocatalyst in combination with the N-doped carbon. Unique f-orbitals of Ce can induce distinctive electronic behavior to the catalyst that helps to form stable coordination structures with N-doped carbons, in addition to its excellent ability to scavenge the OH^● produced during ORRs, therefore helping in catalyst stability. In this study, we have synthesized Ce/N-C catalysts by a metal–organic framework and pyrolysis strategy. The ORR activity of Ce/N-C catalysts has been optimized by systematically increasing the Ce content and performing RDE studies in 0.1 M HClO₄ electrolyte. The Ce/N-C catalyst has been characterized systematically by both physicochemical and electrochemical characterizations. The optimized Ce/N-C-3 catalyst exhibited a half-wave potential of 0.68 V vs. RHE. In addition, the Ce/N-C-3 catalyst also delivered acceptable stability with a loss of 70 mV in its half-wave potential when compared to 110 mV loss for Pt/C (10 wt.%) catalyst, after 5000 potential cycles. When Ce/N-C-3 is used as a cathode catalyst in dual-chamber microbial fuel cells, it delivered a volumetric power density of ~300 mW m⁻³, along with an organic matter degradation of 74% after continuous operation of DCMFCs for 30 days. Full article

The sustainable catalytic efficacy of transition metal oxides (TMO) and rare earth element-based oxides positions them as pivotal materials for effectively treating contaminated wastewater. This study successfully synthesized a series of Ce@MnO₂ photocatalysts using a straightforward hydrothermal method. These photocatalysts were thoroughly characterized for their optical properties, structural morphology, and phase purity. Among the synthesized materials, the Ce@MnO₂ (40:60) exhibited the highest photocatalytic activity for the degradation of Acebutolol (ACB), achieving a remarkable degradation efficiency of 92.71% within 90 min under visible light irradiation. This superior performance is attributed to the increased presence of active species and the efficient separation of photogenerated carriers. Additionally, the photocatalytic reaction mechanism was elucidated, highlighting the catalyst’s surface charge properties which significantly enhanced performance in a solution with pH 8. The outstanding photo-response in the visible spectrum renders this method not only cost-effective but also environmentally benign, presenting a promising approach for large-scale water purification. Full article

The increasing emission of carbon dioxide into the atmosphere has urged the scientific community to investigate alternatives to alleviate such emissions, being that they are the principal contributor to the greenhouse gas effect. One major alternative is carbon capture and utilization (CCU) toward the production of value-added chemicals using diverse technologies. This work aims at the study of the catalytic potential of different cobalt-derived nanoparticles for methanol synthesis from carbon dioxide hydrogenation. Thanks to its abundance and cost efficacy, cobalt can serve as an economical catalyst compared to noble metal-based catalysts. In this work, we present a systematic comparison among different cobalt and cobalt oxide nanocomposites in terms of their efficiency as catalysts for carbon dioxide hydrogenation to methanol as well as how different supports, zeolites, MnO₂, and CeO₂, can enhance their catalytic capacity. The oxygen vacancies in the cerium oxide act as carbon dioxide adsorption and activation sites, which facilitates a higher methanol production yield. Full article

Dry reforming of methane with ratio CH₄/CO₂ = 1 is studied using supported Ni catalysts on SBA-15 modified by CeMnO_x mixed oxides with different Ce/Mn ratios (0.25, 1 and 9). The obtained samples are characterized by wide-angle XRD, SAXS, N₂ sorption, TPR-H₂, TEM, UV–vis and Raman spectroscopies. The SBA-15 modification with CeMnO_x decreases the sizes of NiO nanoparticles and enhances the NiO–support interaction. When Ce/Mn = 9, the NiO forms small particles on the surface of large CeO₂ particles and/or interacts with CeO₂, forming mixed phases. The best catalytic performance (at 650 °C, CH₄ and CO₂ conversions are 51 and 69%, respectively) is achieved over the Ni/CeMnO_x/SBA-15 (9:1) catalyst. The peculiar CeMnO_x composition (Ce/Mn = 9) also improves the catalyst stability: In a 24 h stability test, the CH₄ conversion decreases by 18 rel.% as compared to a 30 rel.% decrease for unmodified catalyst. The enhanced catalytic stability of Ni/CeMnO_x/SBA-15 (9:1) is attributed to the high concentration of reactive peroxo (O⁻) and superoxo (O₂⁻) species that significantly lower the amount of coke in comparison with Ni-SBA-15 unmodified catalyst (weight loss of 2.7% vs. 42.2%). Ni-SBA-15 modified with equimolar Ce/Mn ratio or Mn excess is less performing. Ni/CeMnO_x/SBA-15 (1:4) with the highest content of manganese shows the minimum conversions of reagents in the entire temperature range (X(CO₂) = 4–36%, X(CH₄) = 8–58%). This finding is possibly attributed to the presence of manganese oxide, which decorates the Ni particles due to its redistribution at the preparation stage. Full article

A detailed critical analysis of the scientific literature data concerning catalysts for CO₂ methanation based on nickel supported over oxides was performed. According to the obtained information, it seems that an ionic support is necessary to allow a good nickel dispersion to produce very small nickel metal particles. Such small metal particles result in being very active toward methanation, limiting the production of carbonaceous materials. The use of support and/or surface additives gives rise to medium surface basicity, allowing medium-strong adsorption of CO₂, and it is also advisable to increase the reaction rate. A medium nickel loading would allow the free support geometric surface to be covered densely by small nickel metal particles without the production of larger Ni crystals. It is also advisable to work at temperatures where Ni(CO)₄ formation is not possible (e.g., >573 K). The promising properties of systems based on doped Ni/Al₂O₃, doped with basic and re-active oxides such as MnO_x or/and CeO₂, and those based on Ni/CeO₂ were underlined. Full article

Nitrogen oxides emitted from diesel vehicle exhaust seriously endanger the atmospheric environment and human health, which have attracted people’s attention. Among numerous nitrogen oxide (NO_x) removal technologies, photocatalytic removal of NO_x and SCR have received widespread attention. The photocatalytic treatment of NO_x technology is a good choice due to its mild reaction conditions and low costs. Moreover, NH₃-SCR has been widely used in denitration technology and plays an important role in controlling NO_x emissions. In NH₃-SCR technology, the development of high-efficiency catalysts is an important part. This paper summarizes the research progress of metal oxide catalysts for NH₃-SCR reactions, including V-based catalysts, Mn-based catalysts, Fe-based catalysts, Ce-based catalysts, and Cu-based catalysts. Meanwhile, the detailed process of the NH₃-SCR reaction was also introduced. In addition, this paper also describes a possible SO₂ poisoning mechanism and the stability of the catalysts. Finally, the problems and prospects of metal oxide catalysts for NO_x removal were also proposed. Full article