Search Results (107)

The composite material MgH₂-EEWNi-Cr (20 wt. %) with a hydrogen content of 5.2 ± 0.1 wt.% is characterized by improved hydrogen interaction properties compared to the original MgH₂. The dissociation of the material occurs in three temperature ranges (86–117, 152–162, and 281–351 °C), associated with a complex of effects consisting of changes in the specific surface area of the material, alterations in the crystal lattice during ball milling, and changes in the electronic structure in the presence of a Ni–Cr catalyst, based on first-principles calculations. The decrease in desorption activation energy (E_d = 65–96 ± 1 kJ/mol, ΔE_d = 59–90 kJ/mol) is due to the catalytic effect of N–Cr, leading to a faster decomposition of the hydride phase. Based on the results of ab initio calculations, Ni–Cr on the MgH₂ surface leads to a significant decrease in hydrogen binding energy (ΔE_b = 60%) compared to pure magnesium hydride due to the formation of Ni–H and Cr–H covalent bonds, which reduces the degree of H–Mg ionic bonding. The results obtained allow us to expand our understanding of the mechanisms of hydrogen interaction with storage materials and the possibility of using these as mobile hydrogen storage and transportation materials. Full article

Sulfur compounds in fossil fuels pose significant environmental and industrial challenges, creating a demand for efficient and sustainable desulfurization strategies. Among the available techniques, adsorptive desulfurization has emerged as a promising approach due to its operational simplicity and low energy requirements. In this study, a Ni–Cr modified ZSM-5 zeolite was synthesized to enhance the removal of dibenzothiophene (DBT) from model fuel. The catalyst was prepared by incorporating varying metal loadings and evaluated to identify optimal performance. Structural and chemical characterizations, including FESEM, XRD, NH₃-TPD, FTIR, EDS, and BET analyses, confirmed the successful integration of nickel and chromium within the zeolite framework and demonstrated improved acidity and surface features favorable for adsorption. The catalyst containing 3% chromium and 5% nickel exhibited the highest activity, removing approximately 76% of DBT. Moreover, the optimized material maintained its adsorption efficiency over three consecutive reuse cycles, indicating strong stability and regeneration capability. Overall, the results demonstrate that Ni–Cr/ZSM-5 is a promising and sustainable adsorbent for sulfur removal applications and offers valuable potential for cleaner fuel processing technologies. Full article

The CO₂ hydrogenation process is thought to be one of the feasible methods for producing methanol fuel, which might be used to fulfill future energy demands. Improving the catalytic efficiency and understanding of the process are essential elements for the viability of CO₂ conversion routes. Here, a co-precipitation method was used to synthesize Ni-Cu bimetallic catalysts supported by chromium oxide (Cr₂O₃). To examine nickel (Ni)’s promoting role, the synthesized catalysts were incorporated with different concentrations of Ni. The N₂ adsorption–desorption isotherm exposed the mesoporous nature of Cr₂O₃-based Ni-Cu catalysts. A Fourier Transform Infrared (FTIR) spectroscopy investigation revealed the effective doping of Ni-Cu metal oxides on the surface of Cr₂O₃ by instigating an FTIR absorption band in the region associated with the FTIR absorption of metal oxides. The uniform morphology and homogenous, as well as highly dispersed, form of both Ni and Cu metal were recorded using a Field Emission Scanning Electron Microscope (FESEM) and X-ray Diffraction (XRD) techniques. The surface chemistry, metal–metal, and metal–support interactions of the Ni-Cu/Cr₂O₃ catalysts were disclosed via temperature program reduction (TPR) as well as X-ray photoelectron spectroscopy (XPS). The synergism between the Ni and Cu metals was revealed using both XPS and TPR techniques, which resulted in improving the catalytic profile of Ni-Cu/Cr₂O₃ catalysts. The activity data obtained by applying a slurry reactor demonstrated the active profile of Ni for CO₂ reduction to methanol in terms of the methanol synthesis rate. The promoting role of Ni was established by observing the progressing and linear increase in methanol selectivity by Ni enrichment to the Ni-Cu/Cr₂O₃ catalysts. Structure and activity studies recognized the promoting role of Ni by experiencing metal–metal and metal–support interactions with highly dispersed metal oxides over the Cr₂O₃ support in the current case. Full article

Hexavalent chromium (Cr(VI)), a common contaminant in industrial wastewater, poses severe health risks due to its carcinogenic and mutagenic properties. Consequently, the development of efficient and environmentally friendly methods to reduce Cr(VI) to the less toxic trivalent chromium (Cr(III)) is of great importance. In this study, we present a cost-effective photocatalytic approach using graphitic carbon nitride (g-C₃N₄) modified with 1,3,5-trihydroxybenzene via one-step thermal condensation. The modified photo-catalyst exhibited improved surface area, porosity, visible-light absorption, and a narrowed band gap, all of which contributed to enhanced charge separation. As a result, nearly complete reduction in Cr(VI) was achieved within 90 min under visible-light irradiation. Further optimization of catalyst dosage and EDTA concentration gave even higher reduction efficiency. This work offers a promising strategy for the design of high-performance photocatalysts for environmental remediation. Full article

In this study, chromium ferrite (FeCr; CrFe₂O₄) nanoparticles supported on activated carbon (AC), obtained from agricultural olive mill solid waste, were synthesized via a simple hydrothermal process. The structural, morphological, optical, and chemical properties of the FeCr/AC composite were characterized using XRD, SEM, EDX, DRS, BET, and FTIR techniques. The FeCr/AC composite was applied as a heterogeneous photo-Fenton catalyst for the degradation of methylene blue (MB) dye in an aqueous solution under 25 W visible-light LED irradiation. Critical operational factors, such as FeCr/AC dosage, pH, MB concentration, and H₂O₂ levels, were optimized. Under optimal conditions, 97.56% of MB was removed within 120 min of visible-light exposure, following pseudo-first-order kinetics. The composite also exhibited high efficiency in degrading methyl orange dye (95%) and tetracycline antibiotic (88%) within 180 min, with corresponding first-order rate constants of 0.0225 min⁻¹ and 0.0115 min⁻¹, respectively. This study highlights the potential of FeCr/AC for treating water contaminated with dyes and pharmaceuticals, in line with the Sustainable Development Goals (SDGs) for water purification. Full article

Hexavalent chromium [Cr(VI)] is a hazardous environmental contaminant, and palladium nanoparticles (PdNPs) have shown promise as catalysts for its reduction. This study explores the primary factor influencing the catalytic performance of PdNPs in Cr(VI) reduction by investigating the crystal structure and composition of PdNPs in fungal-based catalysts. Five Pd-loaded catalysts were synthesized by treating fungal biomass with different chemical reagents, resulting in varying Pd(0) contents. The nanoparticle morphology, chemical states, and functional group interactions during Pd adsorption and reduction were investigated using multiple analytical techniques. The results showed that fungal hyphae remained structurally intact throughout the treatment process. PdNPs smaller than 2 nm were observed, with both Pd(0) and PdO present. The proportion of Pd(0) ranged from 6.4% to 37.2%, depending on the chemical reagent used. In addition, functional groups such as phosphate, amine, hydroxyl, and carboxyl were found to play key roles in palladium binding, underscoring the importance of surface chemistry in the adsorption and reduction process. A strong positive correlation was observed between the Pd(0) content and catalytic activity. Notably, the NCPdSF sample (palladium-loaded biomass treated with sodium formate) exhibited the highest Pd(0) content of 59.2% and achieved the most effective Cr(VI) reduction. These results suggest that Pd(0) content is a key determinant of catalytic efficiency in Cr(VI) reduction and that optimizing chemical treatments to enhance Pd(0) levels can substantially improve catalyst performance. Full article

In this study, we designed and synthesized a series of chromium-based polymers (Cr-Ps) and their composites using oxidized carbon nanotubes (O-CNTs) through one-pot ligand engineering. The H₂O₂ production capacity of Cr-Ps increased with an increasing ratio of C–O and Cr–O bonds, which is consistent with the trend observed in the Cr-Ps@O-CNT. The addition of O-CNTs during Cr-Ps synthesis led to a dense structure, which enhanced the electron donor effect and effectively improved the selectivity of the materials for the electrocatalytic production of H₂O₂. Furthermore, during the modulation of different ligands, we observed that the polymers and their complexes formed with terephthalic acid ligands containing para-carboxyl groups had the highest coordination activity and selectivity. The Cr-BDC@O-CNT, using terephthalic acid as the ligand, had the highest C–O and Cr–O densities, resulting in an H₂O₂ yield of 87% in an alkaline solution and an electron transfer number of about 2.2. Compared with Cr-BDC without O-CNTs, its selectivity increased by 32%, due to the higher number of C–O and Cr–O bonds in its dense structure. Moreover, the mass activity of the Cr-BDC@O-CNT reached 19.42 A g⁻¹ at 0.2 V and the Faraday efficiency reached up to 94%, demonstrating excellent electroreduction activity. Our work provides insight into the design of efficient H₂O₂ electrocatalysts through ligand engineering, opening up new ideas for future research. Full article

5-Hydroxymethylfurfural (HMF) is a versatile carbohydrate-derived platform chemical that has been used for the synthesis of a number of commercially valuable compounds. In this study, several chromium (Cr)-doped, biomass-derived hydrochar catalysts were synthesized via the one-pot method using starch, eucalyptus wood, and bagasse as carbon sources. Then, the performance of these synthesized materials for the catalytic conversion of glucose into HMF was evaluated by, primarily, the yield of HMF. The synergistic interactions between the Cr salt and the different biomass components were investigated, along with their effects on the catalytic efficiency. The differences in the catalytic activity of the synthesized materials were analyzed through structural characterization, as well as assessments of the acid density and strength. Among the catalysts, Cr₅BHC₁₈₀ derived from bagasse presented the highest activity, achieving an HMF yield of 64.5% in an aqueous solvent system of dimethyl sulfoxide (DMSO) and saturated sodium chloride (NaCl) at 170 °C after 5 h. After four cycles, the HMF yield of Cr₅BHC₁₈₀ decreased to 38.7%. Characterization techniques such as N₂ adsorption–desorption and Py-FTIR suggested that such a decline in the HMF yield is due to pore blockage and acid site coverage by humic by-products, as demonstrated by the fact that regeneration by calcination at 300 °C restored the HMF yield to 50.5%. Full article

Transition metal dichalcogenides (TMDs) are recognized for their exceptional energy storage capabilities and electrochemical potential, stemming from their unique electronic structures and physicochemical properties. In this study, we focus on chromium disulfide (CrS₂) as the primary research subject and employ a combination of density functional theory (DFT) and first-principle calculations to investigate the effects of incorporating transition metal elements onto the surface of CrS₂. This approach aims to develop a class of bifunctional single-atom catalysts with high efficiency and to analyze their catalytic performance in detail. Theoretical calculations reveal that the Au@CrS₂ single-atom catalyst demonstrates outstanding catalytic activity, with a low overpotential of 0.34 V for the oxygen evolution reaction (OER) and 0.37 V for the oxygen reduction reaction (ORR). These results establish Au@CrS₂ as a highly effective bifunctional catalyst. Moreover, the catalytic performance of Au@CrS₂ surpasses that of traditional commercial catalysts, such as Pt (0.45 V) and IrO₂ (0.56 V), suggesting its potential to replace these materials in fuel cells and other energy applications. This study provides a novel approach to the design and development of advanced transition metal-based catalytic materials. Full article

The design parameters of large-scale iron-chromium redox flow batteries (ICRFB) encompass a wide range of internal and external operational conditions, including electrodes, membranes, flow rate, and temperature, among others. Among these factors, the intrinsic structures of graphite felt (GF) and carbon cloth (CC) play a pivotal role in determining the overall working conditions of ICRFBs. This study systematically investigates the multifaceted relationship between the intrinsic structure of the GF and CC and their impact on the operational performance of ICRFBs. The fundamental difference between the two types of electrodes lies in the intrinsic structure space available in them for electrolyte penetration. A systematic analysis of the structure–activity relation between the electrodes and the initial internal resistance, as well as the operating temperature of the cell, was performed. Additionally, the influence of the electrode structure on critical parameters, including the flow rate, membrane selection (Nafion 212 and Nafion 115), and performance of electrodeposition catalysts (bismuth and indium), is examined in detail. Under varying operating conditions, the intrinsic structures of GF and CC turn out to be a crucial factor, providing a robust basis for electrode selection and performance optimization in large-scale ICRFB systems. Full article

A sustainable and efficient approach for converting carbohydrates into 5-hydroxymethylfurfural (HMF) via heterogeneous catalysis is crucial for effectively utilizing biomass. In this study, we synthesized a series of CrX-polyphenol-formaldehyde resin (PTF) catalysts, which are composites of Cr-doped phenolic-resin-based hydrothermal carbon, using a chelation-assisted multicomponent co-assembly strategy. The performance of the synthesized catalysts was assessed through various analytical techniques, including scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, pyrolysis–Fourier transform infrared spectroscopy, and Brunauer–Emmett–Teller analysis. Cr incorporation into the catalysts enhanced the total and Lewis acidities. Notably, the optimized catalyst, designated as Cr0.6-PTF, achieved an effective glucose conversion into HMF, yielding a maximum of 69.5% at 180 °C for 180 min in a saturated NaCl solution (NaClaq)/dimethyl sulfoxide (2: 18) solvent system. Furthermore, Cr0.6-PTF maintained excellent catalytic activity and a stable chemical structure after nine cyclic reactions, resulting in a 63.8% HMF yield from glucose. This study revealed an innovative approach for utilizing metal-doped phenolic resin hydrothermal carbon to transform glucose into platform chemicals. Full article

This work examines the influence of metal loading and the Ni/Cr ratio of Ni-Cr/SBA-15 catalysts on bioethanol steam reforming for the first time. The characterization of the synthesized samples reveals that higher Cr amounts result in lower Ni crystallite sizes due to the promoting effect of Cr, thereby enhancing the dispersion of the active phase. The catalytic performance has been evaluated in terms of ethanol conversion and H₂ TOF (min⁻¹). Ethanol conversion exhibits an increasing trend with higher Ni content, reaching up to 90% for samples containing 15 wt.%. By increasing the Cr content (lower Ni/Cr ratio) the results evidence a similar trend. A synergistic effect between Ni and Cr was appreciated in conversion values when the Ni content was below 11 wt.% and the Cr content exceeded 2 wt.%, which coincides with a smaller Ni crystallite size. Concerning the H₂ TOF, the catalyst with the lowest Ni content (7 wt.%) exhibited a higher value with a notable enhancement upon increasing the Cr loading. However, a considerable decrease in H₂ TOF was observed for samples with higher Ni loading. Therefore, the best catalytic performance, achieving nearly complete ethanol conversion and high hydrogen production, was reached when using catalysts with 7 wt.% Ni; the Cr loading should be increased to around 2 wt.%. Full article

A series of 5 wt.% Cr/SiO₂ catalysts were prepared through incipient wet impregnation using different chromium salts as a source of Cr (chromium (III) sulfate, acetylacetonate, nitrate, ammonium dichromate). The obtained catalysts were characterized by SEM-EDX, TEM, DRIFT-CD₃CN spectroscopy, UV-VIS diffuse reflectance spectroscopy, and the N₂ low-temperature adsorption–desorption technique. The catalysts were tested in propane, and isobutane dehydrogenation assisted with CO₂ at 600–750 °C. The highest activity in propane dehydrogenation was observed for the catalyst obtained from chromium acetylacetonate, the yield of propylene was 32% at 750 °C, and in the isobutane dehydrogenation reaction, the catalyst obtained from chromium sulfate was the best one; the yield of isobutene was ~30% at 600 °C. The obtained results show that the type of chromium precursor has a significant effect on the efficiency of the catalyst in the propane and isobutane dehydrogenation with CO₂. Full article

In this paper, modified HZSM-5 catalysts with different ratios of chromium (Cr/HZSM-5) were synthesized and the solvent effect of gamma valerolactone (GVL) on the enhancement of levulinic acid (LA) yield was investigated. Characterization of the Cr/HZSM-5 catalyst revealed that the introduction of Cr did not change the structure of HZSM-5. The LA yield was increased from 42.5% (H₂O solvent system) to 51.4% (GVL/H₂O solvent system) under optimal conditions. The influence of GVL on the reaction mechanism was investigated through kinetic analysis, revealing that the incorporation of GVL reduces the activation energy barrier for the conversion of glucose to LA, thereby enhancing the glucose dehydration process. The effect of GVL on the product (LA) was studied, based on molecular dynamics. It was found that the addition of GVL squeezes the water in the solvent system into the second solvation shell layer, which causes GVL to distribute around the carbonyl, hydroxyl, and carboxyl groups of LA, and reduces the likelihood of LA side reactions, thus increasing the yield of LA. Full article

The hybrid sulfur cycle (HyS), as one of the most promising thermochemical cycles for hydrogen production, has received widespread attention in recent years. The HyS contains the sulfur dioxide depolarization electrolysis (SDE) reaction that produces hydrogen, and the anodic reaction process that determines the efficiency of the SDE reaction has become a research focus in this field. In this study, high-temperature pyrolysis technology was used to prepare biomass-based carbon materials from corn stover and analyze their catalytic performance when loaded with platinum–chromium bimetal as an anode catalyst in the SDE reaction. The system investigates the influence of the structure of various components of corn stover (cellulose, holocellulose, and lignin), carbonization conditions, etc., on the structure of the stover-based carbon carrier and then uses it to prepare platinum–chromium bimetallic catalysts for characterization and electrochemical analysis. The results show that the holocellulose-based porous carbon has excellent performance, with a specific surface area reaching 519.81 m²/g and a pore volume of 0.65 cm³/g, and the catalyst can achieve a current density of 780 mA/cm² under a voltage of 1.2 V, showing excellent electrocatalytic performance in the SDE. Therefore, corn stover carbon as a carbon carrier has very high application prospects. Full article