Reduction Of Oxide Research Articles

Formulation and Evaluation of Herbal Anti-Aging Gel based Face Serum from Ficus Carica

Abstract: The popularity of anti-aging face serums as a crucial part of skincare routines has been driven by the desire for youthful and radiant skin. This research aims to provide a comprehensive analysis of the effectiveness behind these serums. By extensively examining scientific literature, we explore the wide range of active ingredients commonly found in these serums, such as retinoids, hyaluronic acid, peptides, antioxidants, and growth factors.we delve into how these ingredients work, including collagen stimulation, hydration retention, oxidative stress reduction, and cellular repair This research focuses on developing an anti-aging serum leveraging the synergistic benefits of aloe vera, green tea extract, and fig fruit oil. The formulation process involves meticulous blending to harness the individual properties of each ingredient, aiming to create a potent solution for combating signs of ageing. We also consider the clinical evidence supporting the effectiveness of anti-aging face serums, with a particular focus on their ability to reduce wrinkles, improve skin texture, and rejuvenate the overall appearance of the skin. There are various types of serums available, including gel-based and oil-based serum,etc. Various types of evaluation parameters were studied. Our formulation showed good viscosity, pH range was also within limits, it exhibited good spreadability, and serum stability was maintained at all temperatures. By integrating scientific analysis with natural ingredients, this study aimed to contribute to the development of effective skincare solutions.

Synergistic role of MoS2 in gelation-induced fabrication of graphene oxide films.

Supporting materials for electrocatalysts must exhibit relative chemical inertness to facilitate unimpeded movement of gas, and demonstrate electrical conductivity to promote efficient electron transfer to the catalyst. Conventional catalyst electrodes, such as glassy carbon, carbon cloths, or Ni foam, are commonly employed. However, the challenge lies in the limited stability observed during testing due to the relatively weak adhesion between the catalyst and the electrode. Addressing this limitation is crucial for advancing the stability and performance of catalyst-electrode systems in various applications. Here, we suggest a novel fabrication method for a freestanding conducting film, accomplished through gelation, incorporating 1T-MoS2 and graphene oxide. 1T-MoS2 nanosheets play a crucial role in promoting the reduction of graphene oxide (GO) on the Zn foil. This contribution leads to accelerated film formation and enhanced electrical conductivity in the film. The synergistic effect also enhances the film's stability as catalyst supports. This study provides insights into the effective utilization of MoS2 and graphene oxide in the creating of advanced catalyst support systems with potential applications in diverse catalytic reaction.

Organic carbon negatively affects the diversity of soil nitrous oxide reducers in Chinese fir plantations at a regional scale

Large-scale planting of Chinese fir (Cunninghamia lanceolata) can bring considerable economic benefits but also seriously alters soil properties, disrupting soil microbial survival patterns and giving rise to distinct microbial communities. Nitrous oxide (N2O) reduction is the sole recognized biological sink for N2O, thereby playing a critical role in forest nitrogen cycling. However, the distribution of N2O reducers in Chinese fir plantation soils and the underlying factors at a regional scale remain unclear. Here, we assessed the abundance, diversity, and community structure of nosZ I-type N2O reducers in soil samples collected from nine state-owned forest farms in Fujian Province, China. The abundance of nosZ I-type reducers exhibited significant variation across sites, with altitude exerting the greatest influence, positively influencing their abundance. Soil organic carbon (SOC) and dissolved organic carbon (DOC) were the strongest predictors of alpha-diversity. Interestingly, SOC and DOC exhibited a negative association with nosZ I-type reducer alpha-diversity. Additionally, DOC played a significant role in influencing community structure. All nosZ I sequences were associated with Alphaprotebacteria and Betaproteobacteria, with Alphaproteobacteria dominating nosZ I-type reducer communities in all soils, accounting for over 90 % of the total sequences. Moreover, the modified stochasticity ratio values exceeded 0.5 at all sampling sites except for one, characterized by the lowest pH and relatively lower nutrient content, indicating the predominance of stochastic processes in community assembly. Taken together, our results provide novel evidence that the augmentation of organic carbon content could potentially reduce diversity and alter the structure of nosZ I-type reducer communities, with potential implications for N2O emissions in Chinese fir plantations.

Biogas as a sustainable and viable alternative fuel for diesel engines: A comprehensive review of production, purification, economic analysis and performance evaluation

Economic and environmental concerns have propelled alternative fuel research in the last few decades. Numerous research initiatives have been undertaken to optimize energy demand by exploring alternative fuels. This comprehensive review presents an in-depth analysis of the current and future prospects of biogas production, filtration and engine applications. To evaluate the performance and emission characteristics of biogas in compression ignition engines, its impact has been extensively analyzed. The study finds that using biogas as an alternate fuel in a dual-fuel mode engine leads to a degradation of 5–27% in performance parameters such as brake thermal efficiency, while brake-specific fuel consumption increases by up to 33%. A subsequent study of emissions reveals a 25–65% reduction in nitrogen oxides and smoke emissions. In contrast, the dual-fuel engine showed a 31% increase in hydrocarbon and carbon monoxide emissions when compared to a conventional diesel engine. In conclusion, biogas has emerged as a promising alternative fuel for diesel engines due to its sustainable nature and potential for reducing emissions. While there are certain trades-offs in terms of performance parameters, the reduction in harmful emissions makes it a viable option for future research and development.

Room Temperature Reduction of Nitrogen Oxide on Iron Metal-Organic Frameworks.

Nitrogen oxides represent one of the main threats for the environment. Despite decades of intensive research efforts, a sustainable solution for NOx removal under environmental conditions is still undefined. Using theoretical modelling, material design, state-of-the-art investigation methods and mimicking enzymes, we have found that selected porous hybrid iron(II/III) based MOF material are able to decompose NOx, at room temperature, in the presence of water and oxygen, into N2 and O2 and without reducing agents. This paves the way to the development of new highly sustainable heterogeneous catalysts to improve air quality. This article is protected by copyright. All rights reserved.

Probiotic Pediococcus acidilactici Strains Exert Anti-inflammatory Effects by Regulating Intracellular Signaling Pathways in LPS-Induced RAW 264.7 Cells.

This study investigated the anti-inflammatory effects of Pediococcus acidilactici strains isolated from fermented vegetables on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. In addition, the probiotic characteristics and safety were evaluated. Our results show that Ped. acidilactici strains possess high survivability in simulated gastrointestinal environments and strong attachment to HT-29 cells. All Ped. acidilactici strains exhibited γ-hemolysis and resistance to gentamicin, kanamycin, and streptomycin, a characteristic commonly observed in lactic acid bacteria. Treatment with Ped. acidilactici inhibited the expression of inducible nitric oxide synthase and cyclooxygenase-2, leading to a subsequent reduction in nitric oxide and prostaglandin E2 production. Furthermore, the strains downregulated interleukin (IL)-1β and IL-6 mRNA levels, ultimately suppressing their production. We demonstrated that Ped. acidilactici strains could modulate the activation of nuclear factor-κB, mitogen-activated protein kinase, and activator protein-1, which are known to regulate inflammatory responses. Consequently, the anti-inflammatory properties of Ped. acidilactici strains in this study support their potential application as therapeutic agents for inflammatory diseases, providing molecular insights into next-generation functional probiotic products.

An Overview Analysis of Current Research Status in Iron Oxides Reduction by Hydrogen

This paper focuses on the study of current knowledge regarding the use of hydrogen as a reducing agent in the metallurgical processes of iron and steel production. This focus is driven by the need to introduce environmentally suitable energy sources and reducing agents in this sector. This theoretical study primarily examines laboratory research on the reduction of Fe-based, metal-bearing materials. The article presents a critical analysis of the reduction in iron oxides using hydrogen, highlighting the advantages and disadvantages of this method. Most experimental facilities worldwide employ their unique original methodologies, with techniques based on Thermogravimetric analysis (TGA) devices, fluidized beds, and reduction retorts being the most common. The analysis indicates that the mineralogical composition of the Fe ores used plays a crucial role in hydrogen reduction. Temperatures during hydrogen reduction typically range from 500 to 900 °C. The reaction rate and degree of reduction increase with higher temperatures, with the transformation of wüstite to iron being the slowest step. Furthermore, the analysis demonstrates that reduction of iron ore with hydrogen occurs more intensively and quickly than with carbon monoxide (CO) or a hydrogen/carbon monoxide (H2/CO) mixture in the temperature range of 500 °C to 900 °C. The study establishes that hydrogen is a superior reducing agent for iron oxides, offering rapid reduction kinetics and a higher degree of reduction compared to traditional carbon-based methods across a broad temperature range. These findings underscore hydrogen’s potential to significantly reduce greenhouse gas emissions in the steel production industry, supporting a shift towards more sustainable manufacturing practices. However, the implementation of hydrogen as a primary reducing agent in industrial settings is constrained by current technological limitations and the need for substantial infrastructural developments to support large-scale hydrogen production and utilization.

Screening of Metal Reduction Potential for Thermochemical Hydrogen Storage

The screening of all non-radioactive metals without lanthanides for thermochemical hydrogen storage was performed based on physical chemistry calculations. The thermodynamic data were collected from the NIST (National Institute of Standards and Technology) public data repository, which was followed by calculations regarding the change in enthalpy, entropy, Gibbs free energy and equilibrium reaction temperature. The results were critically evaluated based on thermodynamic parameters, viable metals were identified, and their hydrogen storage densities and energy–enthalpy ratios were evaluated. The elements viable for controlled thermochemical hydrogen storage via the reversible reduction and oxidation of metal oxides and metals are manganese (Mn), iron (Fe), molybdenum (Mo) and tungsten (W). Manganese has the largest theoretical potential for hydrogen storage with reversible reduction and oxidation of metal oxides and metals. The second candidate is iron, while the other two (Mo and W) have much lower potential. More research efforts should be dedicated to experimental testing of the identified metals (Mn, Fe, Mo and W) and their different oxides for thermochemical hydrogen storage capabilities both on laboratory and pilot scales. Ferromanganese alloy(s) might also prove itself as an efficient and affordable thermochemical hydrogen storage material. Our theoretical investigation expanded the knowledge on thermochemical hydrogen storage and is accompanied with a brief literature review revealing the lack of experimental studies, especially on oxidation of metals with water vapor occurring during the hydrogen release phase of the cycle. Consequently, accurate modelling of transport, kinetics and other phenomena during hydrogen storage and release is scarce.

One-Pot Synthesis of Functionalised rGO/AgNPs Hybrids as Pigments for Highly Conductive Printing Inks.

This work provides a method for the development of conductive water-based printing inks for gravure, flexography and screen-printing incorporating commercial resins that are already used in the printing industry. The development of the respective conductive materials/pigments is based on the simultaneous (in one step) reduction of silver salts and graphene oxide in the presence of 2,5-diaminobenzenesulfonic acid that is used for the first time as the common in-situ reducing agent for these two reactions. The presence of aminophenylsulfonic derivatives is essential for the reduction procedure and in parallel leads to the enrichment of the graphene surface with aminophenylsulfonic groups that provide a high hydrophilicity to the final materials/pigments.

Plasma in Liquids induced modification of Cu surfaces

Plasma in Liquids induced modification of Cu surfaces

Chemical Potential Analysis as an Alternative to the van't Hoff Method: Hypothetical Limits of Solar Thermochemical Hydrogen.

The van't Hoff method is a standard approach for determining reaction enthalpies and entropies, e.g., in the thermochemical reduction of oxides, which is an important process for solar thermochemical fuels and numerous other applications. However, by analyzing the oxygen partial pressure pO2, e.g., as measured by thermogravimetric analysis (TGA), this method convolutes the properties of the probe gas with the solid-state properties of the examined oxides, which define their suitability for specific applications. The "chemical potential method" is here proposed as an alternative. Using the oxygen chemical potential ΔμO instead of pO2 for the analysis, this method does not only decouple gas-phase and solid-state contributions but also affords a simple and transparent approach to extracting the temperature dependence of the reduction enthalpy and entropy, which carries important information about the defect mechanism. For demonstration of the approach, this work considers three model systems; (1) a generic oxide with noninteracting, charge-neutral oxygen vacancy defects, (2) Sr0.86Ce0.14MnO3(1-δ) alloys with interacting vacancies, and (3) a model for charged vacancy formation in CeO2, which reproduces the extensive experimental TGA data available in the literature. The reduction behavior of these model systems obtained from the chemical potential method is correlated with simulated results for the thermochemical water splitting cycle, highlighting the exceptional behavior of CeO2, which originates from defect ionization. The theoretical performance limits for solar thermochemical hydrogen within the charged defect mechanism are assessed by considering hypothetical materials described by a variation of the CeO2 model parameters within a plausible range.

Fatty acids in Plantago asiatica seeds are responsible for the production of the pro-inflammatory mediator nitric oxide

Background: Plantago asiatica L. (Plantaginaceae) commonly grows in East Asia, with its seeds (Shazenshi), having been used as diuretic and anti-inflammatory drugs in traditional Japanese medicine. It is not known which constituents of P. asiatica seeds elicit the anti-inflammatory effects, such as reduced expression of the inducible nitric oxide synthase (iNOS) in interleukin (IL)-1β-treated hepatocytes which leads to a reduction in the pro-inflammatory mediator nitric oxide (NO). Objective: To identify the anti-inflammatory constituents of P. asiatica seeds, the anti-inflammatory activity of purified constituents was determined by assaying NO production in IL-1β-treated hepatocytes. Methods: P. asiatica seeds were extracted with 50% methanol and successively fractionated into three crude fractions with ethyl acetate (EtOAc) and n-butanol. The compounds were methylated and analyzed by gas chromatography–mass spectrometry (GC–MS). Primary cultured rat hepatocytes were prepared by collagenase perfusion, and P. asiatica seed extract (PASE), a fraction, or a compound was added to the culture medium with IL-1β and incubated at 37 °C. Potency of each fraction was determined by the Griess method for measuring the levels of nitrite in the medium. Results: PASE suppressed IL-1β-induced NO production without showing cytotoxicity, and an EtOAc-soluble fraction of PASE significantly inhibited NO production. GC–MS analysis detected 26 distinct fatty acids as their methyl esters in this fraction. Among them, three unsaturated fatty acids (linoleic, oleic, and α-linolenic acids) and palmitic acid were abundant. These unsaturated fatty acids are known to reduce NO levels. In contrast, acteoside and aucubin, which are thought to be present in the n-butanol-soluble fraction, showed only a low level of NO production suppression. Conclusion: The EtOAc-soluble fraction of PASE included many fatty acids, which may suppress the production of NO. The results imply that the anti-inflammatory activity of P. asiatica seeds may be produced by three unsaturated fatty acids. Because the fatty acids are abundant in the seeds of medicinal plants, they are likely to contribute to anti-inflammatory activity of the seeds. Keywords: Plantain seed, polyunsaturated fatty acid, Kampo medicine, hepatocyte, nitric oxide.

Atmospheric Oxidation Capacity Elevated during 2020 Spring Lockdown in Chengdu, China: Lessons for Future Secondary Pollution Control.

This study presents the measurement of photochemical precursors during the lockdown period from January 23, 2020, to March 14, 2020, in Chengdu in response to the coronavirus (COVID-19) pandemic. To derive the lockdown impact on air quality, the observations are compared to the equivalent periods in the last 2 years. An observation-based model is used to investigate the atmospheric oxidation capacity change during lockdown. OH, HO2, and RO2 concentrations are simulated, which are elevated by 42, 220, and 277%, respectively, during the lockdown period, mainly due to the reduction in nitrogen oxides (NOx). However, the radical turnover rates, i.e., OH oxidation rate L(OH) and local ozone production rate P(O3), which determine the secondary intermediates formation and O3 formation, only increase by 24 and 48%, respectively. Therefore, the oxidation capacity increases slightly during lockdown, which is partly attributed to unchanged alkene concentrations. During the lockdown, alkene ozonolysis seems to be a significant radical primary source due to the elevated O3 concentrations. This unique data set during the lockdown period highlights the importance of controlling alkene emission to mitigate secondary pollution formation in Chengdu and may also be applicable in other regions of China given an expected NOx reduction due to the rapid transformation to electrified fleets in the future.

Aluminum dynamics in nitrogen‐saturated Andisols in Tokyo

AbstractThe debate over whether forests around the Tokyo metropolitan area are nitrogen (N) saturation persists, as atmospheric N deposition in throughfall has decreased. This decrease is evidenced by a notable decline in samples collected in the 1990s (especially 1991–1992 and 1995). This decline can be attributed to a reduction in nitrogen oxide (NOx) emissions from automobiles. The acidity derived from N deposition can increase aluminum (Al) mobility. We conducted a monitoring study from September 2010 to December 2021 to elucidate the effects of decreased N deposition on Al concentrations and flux in a forested Andisol. Throughfall and soil‐percolated water samples were collected under stands of Japanese cedar and Japanese cypress in Hachioji, Tokyo (Field Museum Tamakyuryo). Major inorganic ions were determined by ion chromatography. Total Al concentrations were determined using atomic absorption spectrometry after concentration under acidic conditions. Aluminum and nitrate () concentrations were significantly correlated in the both Japanese cedar and Japanese cypress stands. In the case of the Japanese cedar stand, Al concentrations tended to decrease over time from November 2010 to May 2015. Based on stepwise multiple regression analysis, acid load associated with N transformation ([H+]load) was chosen as the sole factor affecting Al mobilization in the Japanese cedar stand. Decreased N deposition affects Al dynamics via a decrease in [H+]load.

Preclinical and Clinical Studies on the Use of Extracellular Vesicles Derived from Mesenchymal Stem Cells in the Treatment of Chronic Wounds.

To date, the widespread implementation of therapeutic strategies for the treatment of chronic wounds, including debridement, infection control, and the use of grafts and various dressings, has been time-consuming and accompanied by many challenges, with definite success not yet achieved. Extensive studies on mesenchymal stem cells (MSCs) have led to suggestions for their use in treating various diseases. Given the existing barriers to utilizing such cells and numerous pieces of evidence indicating the crucial role of the paracrine signaling system in treatments involving MSCs, extracellular vesicles (EVs) derived from these cells have garnered significant attention in treating chronic wounds in recent years. This review begins with a general overview of current methods for chronic wound treatment, followed by an exploration of EV structure, biogenesis, extraction methods, and characterization. Subsequently, utilizing databases such as Google Scholar, PubMed, and ScienceDirect, we have explored the latest findings regarding the role of EVs in the healing of chronic wounds, particularly diabetic and burn wounds. In this context, the role and mode of action of these nanoparticles in healing chronic wounds through mechanisms such as oxygen level elevation, oxidative stress damage reduction, angiogenesis promotion, macrophage polarization assistance, etc., as well as the use of EVs as carriers for engineered nucleic acids, have been investigated. The upcoming challenges in translating EV-based treatments for healing chronic wounds, along with possible approaches to address these challenges, are discussed. Additionally, clinical trial studies in this field are also covered.

Graphene and Natural Products: A Review of Antioxidant Properties in Graphene Oxide Reduction.

This review article addresses the antioxidant properties of different natural products, including ascorbic acid, gallic acid, oxalic acid, L-glutathione (GSH), bacteriorhodopsin, green tea polyphenols, glucose, hydroxycinnamic acid, ethanoic acid, betanin, and L-glutathione, in the reduction of graphene oxide (rGO). rGO can cause damage to cells, including oxidative stress and inflammation, limiting its application in different sectors that use graphene, such as technologies used in medicine and dentistry. The natural substances reviewed have properties that help reduce this damage, neutralizing free radicals and maintaining cellular integrity. This survey demonstrates that the combination of these antioxidant compounds can be an effective strategy to minimize the harmful effects of rGO and promote cellular health.

Open Circuit Interaction Between Ethanol or 2-Propanol and Oxidized Platinum Surfaces.

The interaction between organic molecules and oxidized catalyst surfaces has been used to study the fuel crossover from the anode to the cathode in direct liquid fuel cells. In such experiments, the oxidized surface is put in contact with the fuel under open circuit conditions, and the potential is registered. The open circuit potential (OCP)can then inform on the reactivity of the fuel with the oxidized surface and provide valuable information.Hereinwe present an experimental investigation of the OC interaction between ethanol or 2-propanol with oxidized platinum surfaces. Besides the OCP, we have also employed cyclic voltammetry and fast oxide reduction sweep in the presence of the alcohols. Comparable reaction currents are obtained in the voltammogram, but the electro-oxidation of 2-propanol sets in at considerably lower overpotentials than that of ethanol. At the high potential region, both the magnitude and the potential of the current peak are nearly identical in both cases. Under open circuit conditions, the interaction of ethanol with the oxidized platinum surface is more pronounced than that found for 2-propanol, and these results are corroborated by the facile reduction of the platinum oxides along the fast backward sweep for the latter.

Nitrous acid electroreduction on macroporous silver foam

In this paper, silver 3D foams have been synthesized using dynamic hydrogen bubble template and thiocyanate-based deposition bath. The material was used as electrocatalyst for nitrous acid (HNO2) reduction. On this material, we found that overpotential of nitrous acid reduction is decreased by at least 300 mV and the in situ formed nitric oxide (NO) reduction becomes the predominant step when the potential is decreased even further, comparing to flat silver polycrystalline electrode. Another difference between this material and the silver polycrystalline electrode concerns the influence of the nature of supporting electrolyte on the preferred reaction. Precisely, while Ag polycrystalline is preferentially reducing HNO2 into NO in low concentration of perchlorate electrolyte, Ag foam preferentially reduces the in situ formed NO into N2O, in all tested electrolytes, if the same potential range is considered. The initial reduction of HNO2 into NO is better evidenced after the partial removal of thiocyanate species. Finally, the use of isotope 15N in the nitrite salt and of a flow thin layer cell enabled the detection of nitrogen among other gaseous products for both silver foam and flat silver electrode.

Water extraction in aero gas turbines for contrail mitigation

Abstract Water vapour and particles in aero engine exhaust can give rise to condensation trails (contrails) in the wake of aircrafts, and recent studies suggest that persistent contrails and contrail cirrus account for circa 50% of the total aviation-derived radiative forcing (RF). The Schmidt-Appleman criterion is widely used to qualitatively predict the formation of contrails. The criterion indicates that the formation of contrails is affected by both aero engine exhaust and ambient air conditions and can therefore provide the theoretical basis to devise contrail mitigation strategies and further allows quantitative assessment of these strategies. This work focuses on water extraction from the aircraft engine exhaust for contrail mitigation. The fuel water emission index ( ${\rm{E}}{{\rm{I}}_{{{\rm{H}}_2}{\rm{O}}}}$ ) is one of the key factors that determines whether persistent contrails form or not. It indicates the amount of water produced for every kg of fuel burnt. Research has indicated that water extraction from the exhaust of the aero engine has been considered for Nitrogen oxides (NOx) reduction, but not for contrail mitigation. Assuming that water extraction is indeed possible, the emphasis of this work will therefore be on understanding how much water is needed to be extracted for contrail mitigation depending on the altitude and the relative humidity (RH), with the aim to carry out a meaningful study on the mitigation of persistent contrails and contrail cirrus to enable a fast and considerable reduction in aviation-derived RF.

Computational Insights on Structural Sensitivity of Cobalt in NO Electroreduction to Ammonia and Hydroxylamine.

It has been reported that it was selective to produce ammonia on metallic cobalt in the electrocatalytic nitric oxide reduction reaction (eNORR), where hexagonal close-packed (hcp) cobalt outperforms face-centered cubic (fcc) cobalt. However, hydroxylamine is more selectively produced on a cobalt single-atom catalyst (Co-SAC). Herein, we uncover the structural sensitivity over hcp-Co, fcc-Co, and Co-SAC in eNORR by employing a recently developed constant potential simulation method and microkinetic modeling. It was found that the superior activity for ammonia production on hcp-Co can be attributed to its facile electron and proton transfer and a stronger lateral suppression effect from NO* over fcc-Co. The exceptional hydroxylamine selectivity on Co-SAC is due to the modified electronic structure, namely, a positively charged active center. It was found that it is more favorable to produce NOH* over hcp-Co and fcc-Co, while HNO* is more preferable on Co-SAC, which are firmly correlated with the vertical and strong NO adsorption on the former and the moderate adsorption on the latter. In other words, a key factor for selectivity control is the first step of NO* protonation. Therefore, the local structure and electronic structure of the catalysts can be critical in regulating the activity and selectivity in eNORR.