Reduction Of Oxide Research Articles

Study on the Integration Path of “Photovoltaic + Rural Revitalization” under the Perspective of “Dual Carbon”

Abstract This study combines photovoltaic (PV) technology with rural revitalization, constructs a new long-term mechanism by using a BOT model, and applies fuzzy number processing to the model of the real option method to dig out the potential value of the project. Based on the field research of X county, the article comprehensively analyzes the PV power generation project in terms of economic and social benefits and its impact on poverty alleviation. The results show that the total benefit of X county can reach 3720.34 million yuan in 30 years, and the average annual benefit is about 124.011 million yuan. The full power generation capacity of the project is 4,987 MWh, and the total income from electricity sales reaches 471,985,000 yuan. The PV power project has contributed significantly to environmental protection, with reductions in carbon dust, carbon dioxide, sulfur dioxide, and nitrogen oxides of 12.12 billion tons, 44.61 billion tons, 13.77 billion tons, and 750 million tons, respectively. The study also found that villages with larger administrative territory and suitable topographic conditions are more ideal for establishing large-scale PV ground power plants to help alleviate poverty. Meanwhile, villages with good grid quality are more efficient in reducing poverty when implementing PV poverty alleviation programs. This study provides an innovative perspective for village revitalization strategies and demonstrates the great potential of PV technology in promoting village economic development and environmental protection.

Supercapacitive properties of carbazole-containing cobalt(II) phthalocyanines/reduced graphene oxide composites.

This study aims to compare the effect of substituents (position and number) and reduced graphene oxide on the supercapacitive properties of cobalt(II) phthalocyanines. For this purpose, three new tetra- and octa-substituted cobalt(II) phthalocyanines bearing 9H-carbazol-2-yloxy groups on peripheral or non-peripheral positions (1-3) were synthesized. The characterization of the resultant cobalt(II) phthalocyanines was carried out by applying several spectroscopic approaches. The newly synthesized macromolecules were used for the functionalization of reduced graphene oxide (rGO). The obtained nanocomposites (rGO-(1-3)) were utilized for the modification of Ni foam (NiF) electrodes through a facile one-step electrodeposition strategy performed for electrochemical supercapacitor applications. Simultaneous polymerization of the cobalt phthalocyanines and electrochemically reduction of graphene oxide led to the formation of a fabricating layer on the surface of the NiF electrode. The resulting electropolymerized films were characterized by Raman, Fourier-transform infrared (FT-IR), and Field emission scanning electron microscope (FESEM) spectroscopic techniques as well as electrochemical methods. The prepared electrodes possessed superior electrochemical activities owing to the synergistic effect of the cobalt(II) phthalocyanines and rGO. All the modified electrodes displayed high supercapacitaive properties and the highest activity was obtained for the NiF/rGO2-1 electrode. The NiF/rGO2-1 electrode exhibited higher specific capacitance (655.2 F g-1 at 0.5 A g-1) than NiF/1 (338.0 F g-1). Additionally, a specific capacitance of 85.2% was obtained for NiF/rGO2-1 electrode after 3000 charge-discharge cycles. As a result, all the prepared metallophthalocyanines-reduced graphene oxide can be considered alternative agents to develop high performance-next-generation energy storage devices.

Coumarin and eugenol ameliorate LPS-induced inflammation in RAW 264.7 cells via modulating the NLRP3 inflammasome pathway

Objective: To investigate the underlying mechanism of anti-inflammatory action of coumarin and eugenol in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Methods: RAW 264.7 cells were treated with 2.5 μg/mL of LPS, 50 μM of coumarin, and 50 μM eugenol for 24 h. The viability of the cells was assessed using MTT assay. The production of nitric oxide was determined using Griess reagent and DCFH-DA was used to measure the production of reactive oxygen species. The protein expression of NLRP3, IL-1β, NF-κB, and cyclooxygenase 2 was assessed using Western blot analysis. Results: Coumarin and eugenol showed anti-inflammatory effects against LPS-induced inflammatory response by ameliorating the expression of NLRP3 inflammasome and NF-κB, which further led to a subsequent reduction in IL-1β, nitric oxide, and reactive oxygen species. Conclusions: Coumarin and eugenol exert their anti-inflammatory activities by modulating the NLRP3 inflammasome pathway and NF-κB. These compounds may have promising therapeutic applications for the treatment of various inflammatory diseases.

Exactly regulated copper catalysts exploiting isolated photoelectrochemical reduction of cuprous oxides and random mesh-structured TiO2 for enhanced photoelectrochemical CO2 conversion

This work presents a novel photocorrosion paradigm to guide CO2RR photocathode design. The isolated photoelectrochemical reduction corrosion (IPRC) method developed through this artificial control provides an efficient route to ensure long-term stability, energy saving, and high performance.

Discovery of novel coumarin triazolyl and phenoxyphenyl triazolyl derivatives targeting amyloid beta aggregation-mediated oxidative stress and neuroinflammation for enhanced neuroprotection

CE5, a promising lead compound for Alzheimer's therapy, targets anti-amyloid beta aggregation, oxidative stress reduction, and inflammation modulation mechanisms.

Tracing mitochondrial dysfunction pathways in type 2 diabetes: The promise of mitochondria-targeted therapeutics

The alarmingly high global prevalence of Type 2 Diabetes Mellitus (T2DM) has made novel treatment strategies imperative. One major contributing factor to the onset of T2DM is mitochondrial dysfunction, which deteriorates cellular health, interferes with energy metabolism, and reduces insulin sensitivity. Targeting mitochondrial pathways can enhance outcomes in T2DM. Promising therapeutic benefits can be derived from strategies that target and improve mitochondrial function, biogenesis, efficient turnover, and oxidative stress reduction. Through increased mitochondrial efficiency and improved insulin action, these treatments seek to address the complex problems associated with T2DM. The complexities of mitochondrial dynamics, such as their role in energy production, appropriate regulation of cell death, and creation of reactive oxygen species (ROS), highlight the necessity of comprehensive approaches in the development of medicines that target the mitochondria. This strategy represents a step forward in the management of T2DM and highlights a promising area of cutting edge research in the hunt for potent treatments that might stop or reverse the disease's development, improving patient outcomes and care.

Efficient nitric oxide capture and reduction on Ni-loaded CHA zeolites

As a prominent contributor to air pollution, nitric oxide (NO) has emerged as a critical agent causing detrimental environmental and health ramifications. To mitigate emissions and facilitate downstream utilization, adsorption-based techniques offer a compelling approach for direct NO capture from both stationary and mobile sources. In this study, a comprehensive exploration of NO capture under oxygen-lean and oxygen-rich conditions was conducted, employing Ni ion-exchanged chabazite (CHA-type) zeolites as the adsorbents. Remarkably, Ni/Na-CHA zeolites, with Ni loadings ranging from 3 to 4 wt%, demonstrate remarkable dynamic uptake capacities and exhibit exceptional NO capture efficiencies (NO-to-Ni ratio) for both oxygen-lean (0.17–0.31 mmol/g, 0.32–0.43 of NO/Ni) and oxygen-rich (1.64–1.18 mmol/g) under ambient conditions. An NH3 reduction methodology was designed for the regeneration of absorbents at a relatively low temperature of 673 K. Comprehensive insights into the NOx adsorption mechanism were obtained through temperature-programmed desorption experiments, in situ Fourier transform infrared spectroscopy, and density functional theory calculations. It is unveiled that NO and NO2 exhibit propensity to coordinate with Ni2+via N-terminal or O-terminal, yielding thermally stable complexes and metastable species, respectively, while the low-temperature desorption substances are generated in close proximity to Na+. This study not only offers micro-level perspectives but imparts crucial insights for the advancement of capture and reduction technologies utilizing precious-metal-free materials.

Graphene-based iron single-atom catalysts for electrocatalytic nitric oxide reduction: a first-principles study.

The electrocatalytic NO reduction reaction (NORR) emerges as an intriguing strategy to convert harmful NO into valuable NH3. Due to their unique intrinsic properties, graphene-based Fe single-atom catalysts (SACs) have gained considerable attention in electrocatalysis, while their potential for NORR and the underlying mechanism remain to be explored. Herein, using constant-potential density functional theory calculations, we systematically investigated the electrocatalytic NORR on the graphene-based Fe SACs. By changing the local coordination environment of Fe single atoms, 26 systems were constructed. Theoretical results show that, among these systems, the Fe SAC coordinated with four pyrrole N atoms and that co-coordinated with three pyridine N atoms and one O atom exhibit excellent NORR activity with low limiting potentials of -0.26 and -0.33 V, respectively, as well as have high selectivity toward NH3 by inhibiting the formation of byproducts, especially under applied potential. Furthermore, electronic structure analyses indicate that NO molecules can be effectively adsorbed and activated via the electron "donation-backdonation" mechanism. In particular, the d-band center of the Fe SACs was identified as an efficient catalytic activity descriptor for NORR. Our work could stimulate and guide the experimental exploration of graphene-based Fe SACs for efficient NORR toward NH3 under ambient conditions.

Climatic factors and fertilization rates co-regulate anaerobic methane oxidation driven by multiple electron acceptors in Chinese paddy fields

Paddy fields constitute a substantial anthropogenic reservoir of methane, with their inundation management fostering an ideal habitat for anaerobic methane oxidation. Within this context, a novel clade of anaerobic methanotrophic (ANME) archaea, known as ANME-2d, has been identified as capable of catalyzing anaerobic methane oxidation in conjunction with nitrate and metal oxide reduction processes within paddy fields. Nevertheless, our comprehension of the mechanisms governing anaerobic methane oxidation and its pivotal role in regulating methane emissions within rice paddies remains limited. This study quantified the rates of nitrate- and iron (III)-driven anaerobic methane oxidation through 13C-labeled stable isotope tracing experiments in Chinese paddy fields spanning diverse climate zones. Additionally, it investigated the ANME-2d archaeal community using quantitative polymerase chain reaction and high-throughput sequencing techniques. The nitrate-driven anaerobic methane oxidation contributed 10.9% to methane emission reduction. This contribution is equal to the previously identified contribution of nitrite-driven anaerobic methane oxidation (11.2%) mediated via NC10 bacteria, but played more important roles than iron-driven one (4.1%). The rates of nitrate- and nitrite-driven anaerobic methane oxidation differed significantly among climate zones and showed positive correlation with the mean annual temperature. Furthermore, their rates were more sensitive to temperature increases at higher and lower latitudes, respectively, under both representative concentration pathways 2.6 and 8.5. The rate of anaerobic methane oxidation driven by nitrate exhibited a positive correlation with nitrogen fertilization rate but displayed a negative correlation with phosphorus fertilization rate. Conversely, the rate of anaerobic methane oxidation driven by iron showed no significant correlation with either nitrogen or phosphorus fertilization rates. This study underscores the great potential of anaerobic methane oxidation in mitigating global warming, particularly under the conditions of future climate change and elevated nitrogen loading. These findings underline the necessity of incorporating anaerobic methane oxidation as a crucial parameter in methane emission prediction models.

Nanoscale insights into graphene oxide reduction by tip-enhanced Raman spectroscopy.

Graphene oxide (GO) has attracted substantial interest for its tunable properties and as a possible intermediate for the bulk manufacture of graphene. GO and its reduced derivatives display electronic and optical properties that depend strongly on their chemical structure, and with proper functionalization, GO can have a desirable bandgap for semiconductor applications. However, its chemical activity leads to a series of unclear chemical changes under ambient conditions, resulting in changes in color and solubility upon exposure to light. In this paper, we study the properties of fresh and spontaneously reduced GO under ambient conditions using tip-enhanced Raman spectroscopy (TERS) to map its nanometer scale chemical and structural heterogeneity. We observe different types of defect sites on reduced GO (rGO) by spatially mapping the D to G band peak ratio and D and G band spectral positions. The higher spatial resolution and out-of-plane polarization compared to conventional micro-Raman spectroscopy enables us to resolve unusual features, including D-band shifting on rGO. Based on statistical analysis of the spatial variations in modes and theoretical calculations for different functional groups, we conclude the reduction mechanism of GO is a self-photocatalytic reduction with the participation of water and visible light, in which the rate determining step is electron transport through the metal substrate and ion diffusion on the GO surface. These results demonstrate that TERS can reveal structural and chemical details elucidating reduction mechanisms, through the examination of samples at different time points.

电化学一氧化氮还原合成氨催化剂的研究进展

电化学一氧化氮还原合成氨催化剂的研究进展

Tuning the electrocatalytic nitric oxide reduction activity of copper through alloying with nickel for NH3 production at low overpotentials

The electrocatalytic activity of Cu is significantly improved by alloying with Ni for reduction of NO to NH3. A high FENH3 of about 79% is attained from Cu75Ni25@NC at an overpotential of 610 mV (0.1 V vs. RHE).

Efficient electrocatalytic nitric oxide reduction to ammonia using manganese spinel oxides

CoMn2O4/C is constructed for the electrochemical NO reduction reaction toward NH3, with a maximum NH3 faradaic efficiency of 89.3% at −0.7 V vs. RHE. CoMn2O4/C can promote the hydrogenation of *NO to *NHO (PDS, 0.13 eV) and inhibit the HER.

Selective Electrocatalysis of Nitrous Oxide Reduction Reaction to Nitrogen at Carbon-Supported Pt–Pd–Sn Nanoparticles

Nitrous oxide (N2O) is the third largest greenhouse gas and must be removed using a green method at ambient conditions such as electrocatalysis. Here, we report carbon-supported Pt–Pd–Sn nanoparticles (Pt–Pd–Sn/C)...

Platinum Nanoparticles Supported by Carbon Nanotubes: Improvement in electrochemical sensor performance for caffeine determination.

Platinum nanoparticles supported by carbon nanotubes were obtained by a simple chemical route and used for preparation of electrochemical sensor towards caffeine determination. Carbon nanotubes were used before and after an acid treatment, yielding two different materials. Morphological and structural characterization of these materials showed platinum nanoparticles (size around 12 nm) distributed randomly along carbon nanotubes. Modified electrodes were directly prepared through a dispersion of these materials. Voltammetric studies in the presence of caffeine revealed an electrocatalytic effect of platinum oxides, electrochemically produced from the chemical oxidation of the platinum nanoparticles. This behavior was explored in the development a selective method for caffeine determination based on platinum oxide reduction at a lower potential value (+0.45 V vs. Ag/AgCl). Using the best set of experimental conditions, it was shown a linear relationship for the caffeine concentration ranging from 5.0 to 25 µmol L-1 with a sensitivity of 449 nA L µmol-1. Limits of detection and quantification of 0.54 and 1.80 µmol L-1 were calculated, respectively. Recovery values for real samples of caffeine pharmaceutical formulations between 98.6% and 101.0% (n = 3) were obtained using the proposed procedure. Statistical calculations showed good concordance (95% confidence level) between the added and recovery values.

Characterization of iron nugget produced from iron ore concentrate in a microwave oven using a biomass-based reductant

This study is concerned with the characterization of iron nuggets obtained from the reduction of an iron oxide concentrate in a microwave oven using a biomass-based reducing agent. In the experiments, the concentrate of iron ore consisting of hematite and magnetite minerals supplied from Elazig region and containing 67.29% Fe after enrichment, and as a reducing agent, tea plant wastes containing 94.68% C and 0.03% S after carbonization was used. Carbon required for the reduction of iron oxides to iron was stoichiometrically added to the concentrate with a grain size of -45 µm after its basicity ratio was adjusted. The composite pellets produced after the addition of reducing agent and flux (CaO) were subjected to reduction in a household microwave oven at different times. After the process, optimum (Fe3O4+Fe2O3)/C=1/4, basicity ratio (CaO+MgO)/(SiO2+Al2O3) =1.2 results were obtained. It was seen that the metallic part contained 96.6% Fe, 2.4% C after being separated from the slag and that the metallic phase was separated from the slag very easily. As a result of the microstructure investigations, it was found that the product obtained had similar properties to white cast iron properties.

Oxidative Desulfurization of Simulated Diesel Fuel by Synthesized Tin Oxide Nano-Catalysts Support on Reduced Graphene Oxide

The modified Hummers method was applied to prepare graphene oxide (GO) from the graphite powder. Tin oxide nanoparticles with different loading (10-20 wt.%) supported on reduced graphene oxide were synthesized to evaluate the oxidative desulfurization efficiency. The catalyst was synthesized by the incipient wetness impregnation (IWI) technique. Different analysis methods like FT-IR, XRD, FESEM, AFM, and Brunauer-Emmett-Teller (BET) were utilized to characterize graphene oxide and catalysts. The XRD analysis showed that the average crystal size of graphene oxide was 6.05 nm. In addition, the FESEM results showed high metal oxide dispersions on the rGO. The EDX analysis shows the weight ratio of Sn is close to its theoretical weight. The reduction of metal oxide and (GO) has occurred in one step at temperatures of 400 °C for 2 hours. The performance of the catalysts for dibenzothiophene (DBT) removal using H2O2 as an oxidizing agent was determined under a range of different operating conditions. The results showed that the maximum desulfurization was 71.68% in the best conditions (DBT concentration = 385 ppm, time = 90 min, temperature = 60 oC, catalyst dosage = 0.04g, and amount of oxidant = 0.375 ml).

Hybrid Pore Formation in Copper Spheres by Gas Entrapment and Oxide Reduction

Solid‐state methods for producing porous metals vary greatly in their approaches and outcomes, and they often result in distinctly different pore sizes and/or characteristics. By combining methods in a hybrid process, it is possible that unique porous structures can be made that are simpler to produce, have improved functional properties, or are otherwise superior to any single approach. For the first time, a combination of gas entrapment and oxide reduction to produce microscale porosity in millimeter‐scale copper spheres created by planetary milling is reported. The milling process entraps Ar in micron to submicron pores within the spheres, which are comprised of a Cu 2 mol% CuO metal matrix composite. Upon heating at 800 °C in an inert atmosphere, the individual spheres expand and form ≈29% closed porosity with an average pore size of 1.5 μm. When those spheres are then reheated to 600 °C in a reducing atmosphere, the porosity is converted to being almost entirely open with an average size of 2.3 μm. In addition to the unique nature of the porosity, the processing of the spheres is unusual in that it is completed after only 90 min of milling.

Novel microbial synthesis of rGO nanosheets for effective photocatalytic remediation of Acid Blue 113 dye, improved seed germination, antimicrobial and antioxidant applications

We report for the first time reduction of graphene oxide (GO) nanosheets (NS) by an isolated bacterium from Lonar lake Bacillus cabrialesii RIRD-SK (MCC 4670). Facile, rapid, ecofriendly, and cost-effective biological approach makes it advantageous over physical and chemical methods. Isolated bacterial strain is deposited in Gene Bank accession number MMZ151886. The physiochemical characterization of rGO NS revealed formation of dark black precipitate within 8 h. UV–Visible spectra of rGO shows absorption peak mainly at 269 nm. Fourier-transform infrared spectroscopy (FTIR) revealed presence of functional biomolecules involved in capping and stabilization of NS. X- ray diffraction (XRD) pattern of rGO confirms pure crystal structure. Scanning electron microscopy (SEM) of rGO showed ultrathin graphene NS morphology having thickness less than 3.5 nm. The elemental composition of graphene oxide (GO) and rGO was studied by energy dispersive spectroscopy (EDS) confirms bacterial reduction GO. Specific surface area rGO about 139.53 m2/g was measured by Brunauer-Emmett-Teller (BET) technique. Raman spectroscopy indicates decrease oxygen containing functional group after bacterial reduction with unique fingerprint of material. The rGO NS showed 90.10 % degradation of Acid Blue 113 diazo dye within 45 min. Bioremediation was confirmed with the help of UV–Visible spectroscopy, thin layer chromatography (TLC), FTIR, High-performance liquid chromatography (HPLC) and Liquid chromatography mass spectroscopy (LCMS). Reduced toxicity of the degraded products was observed by the phytotoxicity experiment. A mechanistic degradation pathway has been proposed. rGO NS also exhibit good antimicrobial and antioxidant properties emphasizing its role in biomedical field.

Numerical Study on Compact Design in Marine Urea-SCR Systems for Small Ship Applications

With increasingly stringent emissions legislation, such as that stipulated by the International Maritime Organization, for nitrogen oxide emission reduction in marine diesel engines, the imperative of curtailing nitrogen oxide emissions from marine diesel engines is intensifying. Consequently, the significance of aftertreatment technologies, including diesel particulate filters (DPFs) and selective catalytic reduction (SCR), is poised to grow substantially. In particular, a redesign is required to reduce the size of DPF and SCR systems for application in small ships. In this study, we varied the shape of the filters in DPF and SCR systems, aiming to achieve a distinct flow pattern and enable overall miniaturization. The performance metrics, including the nitric oxide (NO) reduction rate, NH3 slip rate, and pressure drop, of the redesigned models were compared with those of the conventional model. Computational fluid dynamics simulations were used to compare the performance of the redesigned model with that of the conventional model in terms of NO reduction and pressure drop. The redesigned system achieved a NO reduction rate of 6.9% below that of the conventional system, offering additional noteworthy benefits such as a 50% reduction in both pressure and overall length.