Search Results (8,603)

Renewable energy sources have become an urgent worldwide concern due to the impacts of global warming. Globally, biofuels can significantly reduce greenhouse gas emissions, which are major contributors to global warming. The use of biofuels has the potential to transform the energy landscape while mitigating the adverse effects of traditional fossil fuels. This study examines the water features, biochemical compositions, and fatty acid profiles among various plant species. The results reveal significant variations in water features as a consequence of the relative water content and water potential of each seed. Also, we note that some non-edible species like A. blanchetii, C. procera, E. oleracea, P. juliflora, M. oleifera, and J. curcas have good attributes that confer a biofuel-like species. These attributes are high in oil content and have a good profile content of long-chain polyunsaturated fatty acids (LC-PUFAs), ranging from 35% to 80% among the different oilseeds. Fatty acid profiling reveals distinct compositions among the plant species. Stearic acid (C18:0), oleic acid (C18:1), and linoleic acid (C18:2) were the principal oils in A. blanchetii, J. curcas, P. juliflora, M. oleifera, and S. tuberosa compared to other species. M. oleifera stands out with a high linoleic acid (C18:1) content, while C. maxima, J. curcas, and P. juliflora are even higher (C18:2). A principal component analysis (PCA) and Pearson correlations analysis also confirmed that alternative oilseeds exhibited similarities to standard oilseeds and have the potential to replace them for biofuel production. These findings demonstrate the potential of non-conventional oilseeds for sustainable biofuel production. By unlocking their global potential, we can advance towards mitigating environmental impacts and fostering a sustainable biofuel industry. Full article

Environmental contamination has become the most pressing issue in recent years. The value of clean water to mankind has sparked interest in heterogeneous photocatalysis. In this study, a novel photocatalyst has been synthesized by integrating WO₃-doped MoO₃ (WDM) and ZnO through composite formation. The composite nature of the synthesized photocatalyst was confirmed due to the presence of hexagonal ZnO and orthorhombic WDM phases in XRD pattern and scanning electron micrographs. Solid-state absorption spectra and a bandgap analysis showed that WDM-spectral ZnO’s response was better than that of pure ZnO. PL and EIS unveiled the effective role of WDM in suppressing the e⁻–h⁺ recombination process and charge-transfer resistance, respectively, in ZnO. The photocatalytic studies showed that WDM-ZnO was able to remove ~90% of 30 ppm 2-nitrophenol (2-NP) with a rate of 1.1 × 10⁻² min⁻¹, whereas ~65% 2-NP was removed by ZnO (6.1 × 10⁻³ min⁻¹ rate) under the exposure of natural sunlight (800 × 10² ± 100 lx). Moreover, ~52% higher total organic carbon (TOC) removal was observed by WDM-ZnO as compared to ZnO. The photocatalytic removal of 2-NP by the produced photocatalysts followed the Langmuir–Hinshelwood kinetic model, as shown by the kinetic studies. The reactive oxygen species (ROS)-trapping established that the photocatalytic removal mechanism of 2-NP over WDM-ZnO in sunlight illumination was mainly triggered by the superoxide anion (O₂^•−) radical, however, the minor role of hydroxyl (^•OH) radicals cannot be completely ignored. Full article

The development of cost-efficient electrocatalysts for oxygen evolution reaction (OER) with high efficiency is crucial to widespread applications of water splitting for hydrogen production. In this work, porous three-dimensional (3D) amorphous NiFe nanoaggregates composed of interconnected nanograins were synthesized by a cyanogel-based wet chemical reduction method using the NiCl₂/Na₄Fe(CN)₆ cyanogel as the precursor and NaBH₄ as the reducing agent. The influence of the incorporated Fe amount was carefully studied by slightly changing the feeding molar ratios of the Ni/Fe atoms in the precursors. The intrinsic 3D backbone structure of the cyanogel resulted in crystal nuclei tending to generate along with the backbones, which is key to the formation of NiFe nanoaggregates with a porous 3D interconnected structure. The synthesized NiFe nanoaggregates with a 3D interconnected structure and high porosity, as well as the incorporation of Fe, are in favor of high surface area, more active sites, and abundant oxygen vacancies, leading to superior activity and stability of OER in alkaline electrolytes with a low overpotential of 0.35 V at 10 mA cm⁻², a high current density of 24.8 mA cm⁻² at 1.65 V, a small Tafel slope of 76.9 mV dec⁻¹, and attractive durability in 1 M KOH solution. Full article

As a typical organic semiconductor photocatalyst, graphitic carbon nitride (g-C₃N₄) suffers from low photocatalytic activity. In this paper, g-C₃N₄ was prepared by polymerization of dicyandiamide (C₂H₄N₄) in the presence of ammonium chloride (NH₄Cl). It was found that the addition of ammonium chloride can greatly improve the photocatalytic activity of g-C₃N₄ towards CO₂ reduction. The optimal photocatalyst (CN-Cl 20) exhibited a CO₂-to-CO conversion activity of 50.6 μmolg⁻¹h⁻¹, which is 3.1 times that of pristine bulk g-C₃N₄ (BCN) that was prepared in the absence of any ammonium chloride. The enhanced photoactivity of g-C₃N₄ was attributed to the combined effects of chloride modification and an enlarged specific surface area. Chloride modification of g-C₃N₄ can not only reduce the bandgap, but also causes a negatively shifted conduction band (CB) potential level, while ammonia (NH₃) gas from the decomposition of NH₄Cl can act as a gas template to exfoliate layered structure g-C₃N₄, improving the specific surface from 6.8 to 21.3 m²g⁻¹. This study provides new ideas for the synthesis of highly efficient g-C₃N₄-based photocatalytic materials for CO₂ conversion and utilization. Full article

Quinoline (QN) is highly toxic and carcinogenic and has been detected in soil, groundwater, and biological tissues. Advanced oxidation processes (AOPs) have shown promise to address its degradation in wastewater treatment, with catalytic wet peroxide oxidation (CWPO) being highlighted due to its cost-effectiveness and mild operation. However, developing active and inexpensive catalysts is crucial for CWPO’s effectiveness. Another pressing issue is the accumulation of mixed, dirty plastic solid waste (PSW), particularly polyolefins used in packaging. Although recycling rates have increased, much plastic packaging remains in landfills. However, polyolefins can be converted into carbon-based nanostructured materials (CNMs), such as carbon nanotubes (CNTs), through chemical vapor deposition (CVD) using PSW as a carbon precursor. While many studies focus on CNT preparation, their application is often overlooked. In this context, this work proposes the preparation of CNMs, particularly CNTs, through CVD using a single-stage pyrolysis reactor. Polyolefins (LDPE, HDPE, and PP), both individually and in a mixture simulating PSW, were used as carbon sources. Given a sufficiently high temperature, the desired CNT architecture was successfully synthesized regardless of the starting polymer. These CNMs were then tested as catalysts for CWPO in simulated wastewater containing QN. The results showed a rapid degradation of QN (30–120 min) and high removals of total organic carbon (TOC) and aromatic compounds (75% and >90%, respectively), demonstrating the applicability of PSW-derived CNTs in the CWPO process for QN abatement. Full article

We explore the origins of the marked improvement in enantioselectivity in the inner-sphere (PHOX)Pd-catalyzed allylic alkylation of N-benzoyl lactam nucleophiles over their carbocyclic counterparts. We employ density functional theory calculations to aid in the interpretation of experimental results. Ultimately, we propose that the enhancement in enantioselectivity arises primarily from noncovalent interactions between the substrate and ligand rather than secondary substrate chelation, as previously hypothesized. Full article

An efficient approach to a novel family of (Z)-3-amino-3-oxo-1-propenyl selenocyanates was developed based on the reaction of KSeCN with 3-trimethylsilyl-2-propynamides in the presence of ammonium chloride in methanol. The reaction was accompanied by a desilylation process. The products were not formed under the same reaction conditions in the absence of ammonium chloride, which was used for the first time in the reactions of selenocyanates with acetylenes. The use of this new methodology allowed the reaction to carry out in a regio- and stereoselective fashion as anti-addition affording vinyl selenocyanates with a (Z)-configuration in high yields. Full article

The effect of strontium substitution in the structure of the complex oxide Gd₂SrFe₂O₇ on the production of light olefins by CO hydrogenation was investigated. Perovskite-type oxides Gd_2−xSr_1+xFe₂O₇ (x = 0; 0.1; 0.2; 0.3; 0.4) were synthesized by sol–gel technology and characterized by XRD, Mössbauer spectroscopy, BET specific area, acidity testing, and SEM. The experimental data revealed a correlation between the state of iron atoms, acidity, and catalytic performance. It was found that with an increase in the content of Sr²⁺ in the perovskite phase, the basicity of the surface and the oxygen diffusion rate increased. This contributed to the CO dissociative adsorption, formation of active carbon, and its further interaction with atomic hydrogen. Full article

Fluidized catalytic cracking of vacuum gas oil is considered a promising factor in enhancing the gasoline yield to fulfill global energy demands. In this study, a series of FCC catalysts with a zeolite to matrix ratio varying from 18 to 50 was prepared using USY zeolite and amorphous matrix. The matrix was composed of amorphous silica-alumina, kaolin, and silica sol binder. All fresh catalysts were subjected to hydrothermal deactivation treatment at 750 °C for 5 h. The performance evaluation of FCC catalysts was conducted in a fixed bed microactivity test unit, with vacuum gas oil as feed at 550 °C. Comparing a steamed CAT01 sample with a fresh CAT01, the surface area of the steamed sample was 23.3% less. Similarly, the fresh sample CAT05 acidity increased by 102% when compared with the fresh CAT01 sample. As the zeolite to matrix ratio increased, the selectivity of dry gas, LPG, and coke increased, associated with a consistent decrease in gasoline and heavy ends (LCO and HCO). The combined selectivity of product gasoline and LCO with low-zeolite steamed catalyst (CAT01) was 82%, and that of high-zeolite steamed catalyst (CAT05) was 76%. Furthermore, coke selectivity for the steamed CAT01 was 2.1%, whereas 3.7% was observed for the steamed CAT05 sample. The effect of the zeolite to matrix ratio was less pronounced in steamed catalysts as compared with fresh catalysts. Full article

In this study, we employed a chemical solution method to grow zinc oxide (ZnO) nanorods on SnO₂:F (FTO) substrates as photoelectrodes for dye-sensitized solar cells (DSSCs). The influence of varying ZnO nanorod dimensions on cell performance was investigated. Specifically, we explored the effects of nanorod length and diameter on dye adsorption capacity and photovoltaic conversion efficiency. Characterization techniques such as electrochemical impedance spectroscopy (EIS), X-ray diffraction (XRD), and field-emission scanning electron microscopy (FE-SEM) were utilized to analyze the ZnO nanorods. Our results demonstrate that the sequential growth technique allows for control over the length and diameter of ZnO nanorods, thereby modulating their optoelectronic properties. XRD and FE-SEM analyses revealed that the surface morphology of the ZnO nanorods impacts dye adsorption capacity and photovoltaic conversion efficiency. EIS measurements further indicated a significant influence of dye adsorption on the electron lifetime of ZnO nanorods. Overall, this study highlights the potential of multi-step growth of ZnO nanorods to optimize the performance of dye-sensitized solar cells by tuning their morphology and surface properties. Full article

The esterification of oleic acid was applied in order to screen the suitability of a series of phosphotungstic-based Wells-Dawson types of compounds as potential catalysts in the heterogeneous transesterification of sunflower waste cooking oil. This test reaction indicated that the phosphotungstic Wells-Dawson heteropolyacid H₆P₂W₁₈O₆₂·xH₂O, dispersed on titania oxide in a loading of 15 mg per m² of oxide support (named 42% HPA/TiO₂) and possessing exclusively Brønsted acid sites, was the most promising among the screened materials. In addition, the application of a nonlinear analysis methodology to find a surface that fits the specific activity of the oleic acid esterification with methanol at various temperatures, weights of catalyst, molar ratios of substrates, and stirring speeds, and also considering the active phase desorption out of the catalyst’s surface, allowed determining the optimum operative conditions that were applied in the transesterification of the waste cooking oil afterwards. The transesterification of the waste cooking oil at 60 °C and 1:9 WCO: methanol molar ratio in a batch reactor under stirring at 650 rpm for 3 h, catalyzed with 0.25 wt% of 42% HPA/TiO₂ (20.0 g of oil and 49.6 mg of catalyst), presents 74.6% of conversion of glycerides and 74.4% yield towards fatty acid methyl esters. The catalyst was recovered and reused several times, maintaining a fairly constant catalytic performance. Full article

Metal ion doping is the most widely used means to improve the photocatalytic performance of semiconductor materials, which can adjust the band gap, broaden the range of optical response and construct impurity levels. The high efficiency modified NaTaO₃ perovskite catalyst with good structural and catalytic properties was synthesized by a simple hydrothermal reaction method. A variety of analysis and testing techniques, such as XRD, SEM, DRS, XPS and EPR, were used to analyze the structure properties of the prepared materials. The results show that the influence mechanism of different metal introduction on the structure and properties of the NaTaO₃ perovskite was different. Metal doping promoted the bond angle of Ta-O-Ta close to 180°, which restrains the recombination of the photogenerated electron-holes in the crystal. As Ce is introduced into the perovskite, the CeO₂ forms and agglomerates around the perovskite, which improves the electron transport performance. With the narrower band gap, the Ce-modified perovskite shows that the degradation rate of ARS is 84% after 180 min of photoreaction. The species of h⁺, O²⁻ and ·OH play different roles in improving the performance of the photocatalytic degradation process. Full article

Ni-supported SBA-15 catalysts were prepared by physical mixing of Ni(NO₃)₂·6H₂O and SBA-15 (Ni/SBA-15-M) and in the presence of citric acid as the complexing agent (Ni/SBA-15-M-C). Moreover, an Ni-supported SBA-15 catalyst was also prepared by the conventional incipient impregnation method (Ni/SBA-15-I). All the catalysts were systematically evaluated for carbon dioxide reforming of methane (CDR) at CO₂/CH₄ = 1.0, gas hourly space velocity of 60,000 mL·g⁻¹·h⁻¹, and reaction temperature of 700 °C. The characterization results show that the Ni particle size of Ni/SBA-15-M-C is significantly smaller than that of Ni/SBA-15-M due to the coordination effect of citric acid and Ni²⁺. Consequently, the Ni/SBA-15-M-C exhibits superior anti-coking and anti-sintering during the CDR-operated period because of the higher Ni dispersion and stronger Ni–support interaction. Compared to the Ni/SBA-15-I, the physical mixing of nickel salt and mesoporous material for preparing of Ni-based catalyst is easy to operate, although the crystal size and catalytic performance of Ni/SBA-15-C are very similar to that of Ni/SBA-15-M-I. Thus, the efficient and easily controlled catalyst structure makes the physical mixing strategy very promising for preparing highly active and stable CDR catalysts. Full article

The emission of methane leads to the increase in the methane concentration in the atmosphere, which not only wastes resources but also intensifies the greenhouse effect and brings about serious environmental problems. Catalytic combustion can completely convert methane into carbon dioxide and water at low temperatures. However, the catalytic activities of the conventional supported palladium catalysts (e.g., Pd/Al₂O₃ and Pd/ZrO₂) are easy to decrease or the two catalysts can even be deactivated under actual harsh reaction conditions (high temperatures, steam- and sulfur dioxide-containing atmospheres, etc.). Recently, noble metal catalysts supported on zeolites with ordered pores and good thermal stability have attracted much attention. This review article summarizes the recent progress on the development and characteristics of zeolite-supported noble metal catalysts for the combustion of methane. The effects of framework structures, silica/alumina ratios, acidity, doping of alkali metals or transition metals, particle sizes and distributions, and their locations of/in the zeolites on methane combustion activity are discussed. The importance of developing high-performance catalysts under realistic operation conditions is highlighted. In addition, the related research work on catalytic methane combustion in the future is also envisioned. Full article

Xanthan is an extracellular heteropolysaccharide produced by the bacteria Xanthomonas campestris. Due to its unique properties, the polysaccharide and its derivatives are widely used in many industries, from food to biomedicine and oil production, that demands an efficient xanthan depolymerization method to adapt this polysaccharide for various applications. Unlike the known chemical approaches, biological methods are considered to be more environmentally friendly and less energy intensive. In laboratory conditions, we have isolated a bacterial community capable of reducing the xanthan viscosity. Identification of the individual isolates in the microbial community and their testing resulted in the consortium LE-C1, consisting of two microorganisms Paenibacillus phytohabitans KG5 and Cellulosimicrobium cellulans KG3. The specific activities of the overall xanthanase and auxiliary enzymes that may be involved in the xanthan depolymerization were as follows: xanthanase, 19.6 ± 0.6 U/g; β-glucosidase, 3.4 ± 0.1 U/g; α-mannosidase, 68.0 ± 2.0 U/g; β-mannosidase, 0.40 ± 0.01 U/g; endo-glucanase, 4.0 ± 0.1 U/g; and xanthan lyase, 2.20 ± 0.07 U/mg. In order to increase the efficiency of xanthan biodegradation, the LE-C1 whole cells were immobilized in a poly(vinyl alcohol) cryogel. The resulting regenerative biocatalyst was able to complete xanthan depolymerization within 40 cycles without loss of activity or degradation of the matrix. Full article