Reduction Of Oxide Research Articles

Filter Elements Based on Aluminosilicate Fibers for Selective Catalytic Reduction of Nitrogen Oxides — a Review

Filter Elements Based on Aluminosilicate Fibers for Selective Catalytic Reduction of Nitrogen Oxides — a Review

Jasmonic Acid and Salicylic Acid improved resistance against Spodoptera frugiperda Infestation in maize by modulating growth and regulating redox homeostasis

Exploring host plant resistance and elevating plant defense mechanisms through the application of exogenous elicitors stands as a promising strategy for integrated pest management. The fall armyworm, a pernicious menace to grain crops in tropical and subtropical regions, stands as a formidable threat due to its capacity for devastation and a wide-ranging spectrum of host plants. There is no literature regarding artificially induced resistance in maize against fall armyworm (Spodoptera frugiperda) by exogenous application of phytohormones. The present investigation was performed to evaluate the role of jasmonic acid (JA) and salicylic acid (SA) on two maize hybrids namely FH-1046 and YH-1898 against fall armyworm. Results showed that plant height, biomass and lengths, fresh and dry weight of root shoot which decreased with armyworm infestation improved with phytohormonal application. JA treatment resulted in a higher increase in all attributes as compared to SA treatment. Improvement in relative water contents, photosynthetic pigments and pronounced levels of phenol and proline accumulation were observed in infested plants after JA treatment. Infested plants recovered from oxidative stress as JA application activated and increased the antioxidant enzyme activity of superoxide dismutase, peroxidase and polyphenol oxidase activity in both FH-1046 and YH-1898 . The oxidative stress reduction in infested plants after JA treatment was also evident from a fair decrease in MDA and H2O2 in both varieties. The SA and JA mediated genes expression was studied and it was found that in FH1046 maize cultivar, JA dependent genes, particularly marker genes PR1 and Lox5 were highly expressed along with TPS10 and BBT12. Whereas SPI, WRKY28, ICS and PAL were shown to be activated upon SA application. Evidently, both JA and SA elicited a robust defensive response within the maize plants against the voracious S. frugiperda, which in consequence exerted a discernible influence over the pest's developmental trajectory and physiological dynamics. A decrease in detoxification enzyme activity of the insects was observed after feeding on treated plants. Moreover, it was recorded that the survival and weight gain of FAW feeding on phytohormone treated maize plants also decelerated. In conclusion, FH-1046 was found to be more tolerant than YH-1898 against fall armyworm infestation and 1 mM JA was more effective than 1 mM SA for alleviation of fall armyworm stress. Therefore, it was inferred that phytohormones regulated redox homeostasis to circumvent oxidative damage and mediate essential metabolic events in maize under stress. To our current understanding, this study is the very first presentation of induced resistance in maize against S. frugiperda with the phytohormonal application (JA and SA).

Biochar Co-Compost: A Promising Soil Amendment to Restrain Greenhouse Gases and Improve Rice Productivity and Soil Fertility

Agriculture is a major source of greenhouse gas (GHG) emissions. Biochar has been recommended as a potential strategy to mitigate GHG emissions and improve soil fertility and crop productivity. However, few studies have investigated the potential of biochar co-compost (BCC) in relation to soil properties, rice productivity, and GHG emissions. Therefore, we examined the potential of BC, compost (CP), and BCC in terms of environmental and agronomic benefits. The study comprised four different treatments: control, biochar, compost, and biochar co-compost. The application of all of the treatments increased the soil pH; however, BC and BCC remained the top performers. The addition of BC and BBC also limited the ammonium nitrogen (NH4+-N) availability and increased soil organic carbon (SOC), which limited the GHG emissions. Biochar co-compost resulted in fewer carbon dioxide (CO2) emissions, while BC resulted in fewer methane (CH4) emissions, which was comparable with BCC. Moreover, BC caused a marked reduction in nitrous oxide (N2O) emissions that was comparable to BCC. This reduction was attributed to increased soil pH, nosZ, and nirK abundance and a reduction in ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB) abundance. The application of different amendments, particularly BCC, favored rice growth and productivity by increasing nutrient availability, soil carbon, and enzymatic activities. Lastly, BCC and BC also increased the abundance and diversity of soil bacteria, which favored plant growth and caused a reduction in GHG emissions. Our results suggest that BCC could be an important practice to recycle organic sources while optimizing climate change and crop productivity.

Oral edaravone ameliorates behavioral deficits and pathologies in a valproic acid-induced rat model of autism spectrum disorder

Autism spectrum disorder (ASD) is neurodevelopmental disorder with a high incidence rate, characterized by social deficits and repetitive behaviors. There is currently no effective management available to treat the core symptoms of ASD; however, oxidative stress has been implicated in its pathogenesis. Edaravone (EDA), a free-radical scavenger, is used to treat amyotrophic lateral sclerosis (ALS) and acute ischemic stroke (AIS). Here, we hypothesized that an oral formula of EDA may have therapeutic efficacy in the treatment of core ASD symptoms. A rat model of autism was established by prenatal exposure to valproic acid (VPA), and the offsprings were orally treated with EDA at low (3 mg/kg), medium (10 mg/kg), and high (30 mg/kg) doses once daily for 28 days starting from postnatal day 25 (PND25). Oral EDA administration alleviated the core symptoms in VPA rats in a dose-dependent manner, including repetitive stereotypical behaviors and impaired social interaction. Furthermore, oral administration of EDA significantly reduced oxidative stress in a dose-dependent manner, as evidenced by a reduction in oxidative stress markers and an increase in antioxidants in the blood and brain. In addition, oral EDA significantly attenuated downstream pathologies, including synaptic and mitochondrial damage in the brain. Proteomic analysis further revealed that EDA corrected the imbalance in brain oxidative reduction and mitochondrial proteins induced by prenatal VPA administration. Overall, these findings demonstrate that oral EDA has therapeutic potential for ASD by targeting the oxidative stress pathway of disease pathogenesis and paves the way towards clinical studies.

Instantaneous reduction of inkjet-printed graphene oxide on PVDF nanofibers for high-performance ultralight flexible supercapacitors

As the demand for innovative electronic devices continues to grow, flexible electronic products which offer a solution capable of adapting to various shapes and deformations, are increasingly gaining prominence. This study innovatively uses electrospun polyvinylidene fluoride (PVDF) nanofibers as substrates and employs reactive inkjet printing (RIP) technology to deposit and instantaneously reduce graphene oxide (GO), fabricating ultralight flexible all-solid-state supercapacitors. To verify that PVDF nanofibers as substrates can facilitate the uniform deposition of GO ink during inkjet printing and prevent the dispersion of GO into the internal structure, thereby achieving good capacitive performance with the fewest layers of printing, this study analyzes and compares the capacitive performance differences among 1rGO/PVDF, 3rGO/PVDF, and 5rGO/PVDF samples. The results have been confirmed that the GO ink was effectively instantaneously in-situ reduced by l-ascorbic acid (AA) to rGO by RIP system, and the specific capacitance of 1rGO/PVDF electrode was founded of 83.29 F/g at a current density of 2 A/g from the GCD analysis with a corresponding energy density of 7.5 Wh kg−1 and power density of 1.04 kW kg−1. The 1rGO/PVDF supercapacitor exhibits excellent electrochemical stability, maintaining 93 % efficiency after 4000 charge-discharge cycles at a current density of 2 A/g.

Nickel and Molybdenum Composites Decorated Nitrogen-Doped Carbon Catalysts from Spent Coffee Grounds for Alkaline Hydrogen Evolution.

Biomass-derived materials can help develop efficient, environmentally friendly and cost-effective catalysts, thereby improving the sustainability of hydrogen production. Herein, we propose a simple method to produce nickel and molybdenum composites decorated spent coffee grounds (SCG) as an efficient catalyst, SCG(200)@NiMo, for electrocatalytic hydrogen production. The porous carbon supporter derived form SCG provided a larger surface, prevented aggregation during the high temperature pyrolysis, optimized the electronic structure by N and provided a reducing atmosphere for the oxides reduction to form heterojunctions. The sieved SCG showed obvious improvement of HER performance and enhanced conductivity and long-term durability. The obtained SCG(200)@NiMo exhibits the highest electrochemical performance for the hydrogen evolution reaction process, as evidenced by the overpotential of only 127 mV at a current density of ɳ10 and 97.7 % catalytic activity retention even after 12 h of operation. This work may stimulate further exploration of efficient electrocatalysts derived from biomass.

Green iron and syngas production via continuous solar-driven agricultural waste biomass gasification combined with iron(III) oxide reduction

The production of renewable synthetic fuels and chemicals from solar energy and agricultural waste biomass is considered. Solar thermochemical conversion processes offer a promising pathway to a sustainable fuel economy and green chemical industry. This study investigates the continuous solar-driven gasification of agricultural biomass (betel nut waste) combined with iron oxide (Fe2O3) reduction to produce carbon-neutral syngas and green metallic iron in a single process. A thermodynamic analysis of the system was initially conducted to predict the distribution of equilibrium products. Then, on-sun continuous processing was experimentally carried out under different operating conditions, including betel/Fe2O3 molar ratios (0.56–1.5) and temperatures (900–1200 °C) to evaluate the process feasibility and reliability. As a result, solar gasification of betel nut waste combined with Fe2O3 reduction performed exceptionally well with continuous reactant particles feeding, demonstrating a feasible pathway for producing green iron and high-quality syngas. The maximum syngas yield reached 63.3 mmol/gdry_betel, approaching its theoretical value, and high-purity Fe was simultaneously produced. The process demonstrated high efficiency, with maximum carbon conversion approaching 98 %, energy upgrade factor up to 1.26, and solar-to-fuel energy conversion efficiency up to 14.4 %, highlighting remarkable conversion performance of biomass and solar energy to chemicals.

Molecular Changes in the Ischemic Brain as Non-Invasive Brain Stimulation Targets-TMS and tDCS Mechanisms, Therapeutic Challenges, and Combination Therapies.

Ischemic stroke is one of the leading causes of death and disability. As the currently used neurorehabilitation methods present several limitations, the ongoing research focuses on the use of non-invasive brain stimulation (NIBS) techniques such as transcranial magnetic stimulation (TMS) and transcranial direct current stimulation (tDCS). NIBS methods were demonstrated to modulate neural excitability and improve motor and cognitive functioning in neurodegenerative diseases. However, their mechanisms of action are not fully elucidated, and the clinical outcomes are often unpredictable. This review explores the molecular processes underlying the effects of TMS and tDCS in stroke rehabilitation, including oxidative stress reduction, cell death, stimulation of neurogenesis, and neuroprotective phenotypes of glial cells. A highlight is put on the newly emerging therapeutic targets, such as ferroptotic and pyroptotic pathways. In addition, the issue of interindividual variability is discussed, and the role of neuroimaging techniques is investigated to get closer to personalized medicine. Furthermore, translational challenges of NIBS techniques are analyzed, and limitations of current clinical trials are investigated. The paper concludes with suggestions for further neurorehabilitation stroke treatment, putting the focus on combination and personalized therapies, as well as novel protocols of brain stimulation techniques.

Reduced Graphene Oxide Wrapped Polypyrrole on Carbon Cloth for High‐Performance Flexible Solid‐State Supercapacitors

AbstractThe nature of rigidity and low energy density of polypyrrole (PPy)‐based electrodes limits their wide application in flexible energy storage devices. In this study, reduced graphene oxide (rGO) wrapped polypyrrole (PPy)/oxidized carbon cloth (OCC) (rGO@PPy/OCC) is prepared by the polymerization of pyrrole using MnO2 as the oxidant on the surface of OCC followed by the adsorption and reduction of graphene oxide (GO). The prepared rGO@PPy/OCC electrode exhibits a high gravimetric specific capacitance of 547 F g−1 at a current density of 0.5 A g−1 and a high area specific capacitance of 1641 mF cm−2 at a current density of 1.5 mA cm−2. It nearly maintains the initial capacitance after 8000 cycles at a high scan rate of 200 mV s−1 and at a large current density of 10 A g−1. Moreover, the flexible rGO@PPy/OCC electrodes are used to construct flexible solid‐state supercapacitors (FSSC). The FSSC based on rGO@PPy/OCC exhibits a high energy density (33.89 Wh kg−1 and 101.81 µWh cm−2) and a capacitance retention of 95.10% after 1000 bending cycles, demonstrating the excellent cycling stability and flexibility. Therefore, it is potential for rGO@PPy/OCC as a flexible electrode to fabricate high‐performance FSSC.

Advanced manufacturing of high conductive graphene coatings on polyethylene terephthalate substrate through laser-induced processes and thermal optimization

Graphene holds immense promise for applications in sensors due to its exceptional properties such as large carrier mobility and high electrical and thermal conductivities. Nevertheless, the manufacture of high conductive graphene films onto flexible substrates remains a formidable challenge. This paper presented a novel method for the precise incorporation of high conductive graphene coatings onto polyethylene terephthalate (PET) through the back transfer of laser-reduced graphene oxide (LRGO) from Al2O3 ceramic to PET. A record-low sheet resistance for LRGO so far, approximately 12 Ω/sq. was achieved, meantime exhibiting 5B level adhesion performance with PET substrate. The sheet resistance of the transferred LRGO was measured and demonstrated to be adjustable by manipulating laser power, scanning speed, and hatch distance. The analysis of reduction of graphene oxide (GO) involved a comprehensive examination of alterations in topography image, chemical bond content, C/O atomic ratio, and ID/IG intensity ratio. These observations provided insights into the factors contributing to the decrease of sheet resistance within LRGO. The adoption of a continuous gigahertz (GHz) femtosecond laser as the light source, coupled with the incorporation of thermally conductive Al2O3 plate as a heat sink, facilitated the manufacturing processes including reduction and transfer of GO. The manufacture of graphene coatings with high electrical conductivity on PET in a versatile and cost-effective manner, presents significant potential for diverse applications, particularly in conductive-coatings-based sensors.

Thermodynamic modeling of silicon carbide formation during the Acheson process in non-stoichiometric mixtures

A brief review and critical evaluation of the literature related to the mechanism of carbothermic reduction of silicon oxide is presented. To resolve the contradictions in the literature data about the number of chemical reactions and key intermediate substances during the Acheson process, thermodynamic modeling of products of carbothermic reduction of silicon (IV) oxide at 1 bar total pressure was carried out. It was determined that CO2 and Si were absent among the intermediates at temperatures close to the silicon carbide formation temperature (from 1520 to ~2500 °С). Out of several dozen possible reactions, the two dominant reactions that result in the formation of silicon carbide in the Acheson process were identified. The effect of reagents temperature from 1000 to 3000 °С, bulk and local deviation from stoichiometry of the initial mixture on the composition of the reaction products was discovered. Obtained new data explains some empirical observations and greatly simplifies the physicochemical modeling of the Acheson process.

Analysis of Ozone and VOCs Pollution Characteristics, Sources, and Abatement Control Strategies in Hebi

In order to control the increasing ozone （O3） pollution in Hebi, Henan Province, clarifying the pollution characteristics of ozone and its precursors is vital. Therefore, we conducted a comprehensive analysis of O3 pollution utilizing the OFP-PMF-EKMA method combined with online hourly resolution monitoring data of conventional pollutants and volatile organic compounds （VOCs） in the summer of 2022 （June-September）. Ozone formation potential （OFP） was used to identify the key VOCs species, and the PMF model was used to identify the VOCs emission sources, whereas EKMA curves and scenario analysis were used to identify the main ozone control area in Hebi and to determine the reduction ratio of VOCs and NOx in a scientifically refined way. In 2022, Hebi had persistent O3 pollution, with the highest concentration in June. Conditions of high temperature, low humidity, and low atmospheric pressure contributed to the O3 accumulation. Aromatic and oxygenated volatile organic compounds （OVOCs） contributed significantly to the OFP and VOCs fraction, which were the dominant active substance and concentration dominant species. The results of the VOCs source analysis indicated that vehicle exhaust sources （25.3%） were the main source of atmospheric VOCs, followed by process sources （17.7%） and biomass combustion sources （17.6%）. Thus, emission sources associated with the combustion of fossil fuels and industrial production emissions were the most urgent sources of atmospheric VOCs to be controlled in Hebi. The O3 generation in Hebi occurred in the VOCs-sensitive zones, and the emission reduction results showed that a synergistic emission reduction of VOCs and nitrogen oxide （NOx） could effectively control O3 pollution with a 75% reduction in VOCs and a 10% reduction in NOx.

Following the Structural Changes of Iron Oxides during Reduction under Transient Conditions.

Iron is considered as attractive energy carrier in a carbon-free circular energy economy. The reduction of iron oxide is crucial for its applica-tion as a metal fuel as it determines the efficiency of the cycle. Temperature programmed reduction of α-Fe2O3 was monitored by complementary X-ray absorption spectroscopy (XAS) and diffraction (XRD) to obtain the phase composition with high time resolution. Synchrotron Mössbauer spectroscopy (SMS) was additionally employed due to its high sensitivity to the different iron species. Theoretical calculations of surface and bulk adsorption processes were performed to establish the potential reaction pathways and the corresponding energy barriers. A kinetic particle model was then developed to bridge the experimental data and theoretical calculations, which reproduced the reduction onset and behavior. The reduction process was found to be strongly dependent on the heating rate in terms of the reduction window and the observed intermediate species. We propose that a core-shell mechanism determines the reaction by forming an iron layer which subsequently hinders diffusion of water out of the porous particles leading to some unreduced FeO at high temperature. This study demonstrates the need for complementary methods for describing complex heterogeneous systems and overcoming the chemical sensitivity limitations of any single method.

Development and Performance Evaluation Experiment of a Device for Simultaneous Reduction of SOx and PM

Mitigating air pollutants such as SOx and PM emitted from ships is an important task for marine environmental protection and improving air quality. To address this, exhaust gas after-treatment devices have been introduced, but treating pollutants like SOx and PM individually poses challenges due to spatial constraints on ships. Consequently, a Total Gas Cleaning System (TGCS) capable of simultaneously reducing sulfur oxides and particulate matter has been developed. The TGCS combines a cyclone dust collector and a wet scrubber system. The cyclone dust collector is designed to maintain a certain distance from the bottom of the wet scrubber, allowing exhaust gases entering from the bottom to rise as sulfur oxides are adsorbed. Additionally, the exhaust gases descending through the space between the cyclone dust collector and the wet scrubber collide with the scrubbing solution before entering the bottom of the wet scrubber, facilitating the absorption of SOx. In this study, the efficiency of the developed TGCS was evaluated, and the reduction effects based on design parameters were investigated. Furthermore, the impact of this device on ship engines was analyzed to assess its practical applicability. Experimental results showed that increasing the volume flow rate of the cleaning solution enhanced the PM reduction effect. Particularly, when the height of the Pall ring was 1000 mm and the volume flow rate was 35 L/min, the sulfur oxide reduction effect met the standards for Sulfur Emission Control Areas (SECA). Based on these findings, suggestions for effectively controlling atmospheric pollutants from ships were made, with the expectation of contributing to the development of systems combining various after-treatment devices.

Comparative genome analysis of the genus Marivirga and proposal of two novel marine species: Marivirga arenosa sp. nov., and Marivirga salinae sp. nov.

BackgroundThe phylum Bacteroidota represents a significant proportion of heterotrophic bacteria found in marine ecosystems. Members of the phylum Bacteroidota are actively involved in the degradation of biopolymers such as polysaccharides and proteins. Bacteroidota genomes exhibit a significant enrichment of various enzymes, including carbohydrate-active enzymes (CAZymes), carboxypeptidases, esterases, isomerases, peptidases, phosphatases, and sulfatases. The genus Marivirga, a member of the family Marivirgaceae within the phylum Bacteroidota, comprises six documented species. During a microbial diversity study, three novel Marivirga strains (BKB1-2 T, ABR2-2, and BDSF4-3 T) were isolated from the West Sea, Republic of Korea.ResultsTo explore the taxonomic status and genomic characteristics of the novel isolates, we employed a polyphasic taxonomic approach, which included phylogenetic, chemotaxonomic and comprehensive genome analysis. The three isolates were Gram-stain-negative, aerobic, rod-shaped, moderately halophilic, and had a gliding motility. The average nucleotide identity (ANI) and digital DNA-DNA hybridization (dDDH) values among the two isolates, BKB1-2 T and BDSF4-3 T, and the six reference strains were 70.5–76.5% for ANI and 18.1–25.7% for dDDH. Interestingly, the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that the strains harbor genes for a comprehensive pathway for dissimilatory nitrate reduction to ammonium (DNRA), as well as other nitrogen pathways for the reduction of nitrite, nitric oxide, and nitrous oxide. Additionally, the antiSMASH analysis indicated that the strains contained three to eight biosynthetic gene clusters (BGCs) associated with the synthesis of secondary metabolites. Furthermore, the strains carried a high number of CAZyme ranging from 53 to 152, which was also demonstrated by an in vitro analysis of degradation of the polysaccharide cellulose, chitin, laminarin, starch, and xylan. Additionally, all the strains carried genes for the metabolism of heavy metals, and exhibited tolerance to heavy metals, with minimum inhibitory concentrations (MICs) in millimoles (mM) in ranges of Co2+ (3–6), Cu2+ (0.2–0.4), Ni2+ (3–5), Zn2+ (2–4), Mn2+ (20–50), and Hg2+ (0.3).ConclusionsBased on polyphasic taxonomic approach, the three isolated strains represent two novel species names Marivirga arenosa sp. nov. (BKB1-2 T = KCTC 82989 T = InaCC B1618T), and Marivirga salinae sp. nov. (BDSF4-3 T = KCTC 82973 T = InaCC B1619T).

The Conundrum of "Pair Sites" in Langmuir-Hinshelwood Reaction Kinetics in Heterogeneous Catalysis.

Understanding reaction kinetics is crucial for designing and applying heterogeneous catalytic processes in chemical and energy conversion. Here, we revisit the Langmuir-Hinshelwood (L-H) kinetic model for bimolecular surface reactions, originally formulated for metal catalysts, assuming immobile adsorbates on neighboring pair sites, with the rate varying linearly with the density of surface sites (sites per unit area); r ∝ [*]o 1. Supported metal oxide catalysts, however, offer systematic control over [*]o through variation of the active two-dimensional metal oxide loading in the submonolayer region. Various reactions catalyzed by supported metal oxides are analyzed, such as supported VO x catalysts, including methanol oxidation, oxidative dehydrogenation of propane and ethane, SO2 oxidation to SO3, propene oxidation to acrolein, n-butane oxidation to maleic anhydride, and selective catalytic reduction of nitric oxide with ammonia. The analysis reveals diverse dependencies of reaction rate on [*]o for these surface reactions, with r ∝ [*]o n , where n equals 1 for reactions with a unimolecular rate-determining step and 2 for those with a bimolecular rate-limiting step or exchange of more than 2 electrons. We propose refraining from a priori assumptions about the nature and density of surface sites or adsorbate behavior, advocating instead for data-driven elucidation of kinetics based on the density of surface sites, adsorbate coverage, etc. Additionally, recent studies on catalytic surface mechanisms have shed light on nonadjacent catalytic sites catalyzing surface reactions in contrast to the traditional requirement of adjacent/pair sites. These findings underscore the need for a more nuanced approach in modeling heterogeneous catalysis, especially supported metal oxide catalysts, encouraging reliance on experimental data over idealized assumptions that are often difficult to justify.

Cardiovascular effects of breath-hold diving at altitude

ABSTRACT Marabotti C, Laurino M, Passera M, Cialoni D, Franzino E, Benvenuti C, Pingitore A. Cardiovascular effects of breath-hold diving at altitude. Undersea Hyperb Med. 2024 Second Quarter; 51(2):189- 196. Hypoxia, centralization of blood in pulmonary vessels, and increased cardiac output during physical exertion are the pathogenetic pathways of acute pulmonary edema observed during exposure to extraordinary environments. This study aimed to evaluate the effects of breath-hold diving at altitude, which exposes simultaneously to several of the stimuli mentioned above. To this aim, 11 healthy male experienced divers (age 18-52y) were evaluated (by Doppler echocardiography, lung echography to evaluate ultrasound lung B-lines (BL), hemoglobin saturation, arterial blood pressure, fractional NO (Nitrous Oxide) exhalation in basal condition (altitude 300m asl), at altitude (2507m asl) and after breath-hold diving at altitude. A significant increase in E/e’ ratio (a Doppler-echocardiographic index of left atrial pressure) was observed at altitude, with no further change after the diving session. The number of BL significantly increased after diving at altitude as compared to basal conditions. Finally, fractional exhaled nitrous oxide was significantly reduced by altitude; no further change was observed after diving. Our results suggest that exposure to hypoxia may increase left ventricular filling pressure and, in turn, pulmonary capillary pressure. Breath-hold diving at altitude may contribute to interstitial edema (as evaluated by BL score), possibly because of physical efforts made during a diving session. The reduction of exhaled nitrous oxide at altitude confirms previous reports of nitrous oxide reduction after repeated exposure to hypoxic stimuli. This finding should be further investigated since reduced nitrous oxide production in hypoxic conditions has been reported in subjects prone to high-altitude pulmonary edema.

Manganese reduction and associated microbial communities in Antarctic surface sediments.

The polar regions are the fastest warming places on earth. Accelerated glacial melting causes increased supply of nutrients such as metal oxides (i.e., iron and manganese oxides) into the surrounding environment, such as the marine sediments of Potter Cove, King George Island/Isla 25 de Mayo (West Antarctic Peninsula). Microbial manganese oxide reduction and the associated microbial communities are poorly understood in Antarctic sediments. Here, we investigated this process by geochemical measurements of in situ sediment pore water and by slurry incubation experiments which were accompanied by 16S rRNA sequencing. Members of the genus Desulfuromusa were the main responder to manganese oxide and acetate amendment in the incubations. Other organisms identified in relation to manganese and/or acetate utilization included Desulfuromonas, Sva1033 (family of Desulfuromonadales) and unclassified Arcobacteraceae. Our data show that distinct members of Desulfuromonadales are most active in organotrophic manganese reduction, thus providing strong evidence of their relevance in manganese reduction in permanently cold Antarctic sediments.

Facile Synthesis of U2Ti Intermetallic by Direct Electrochemical Reduction of UO2-TiO2 Composite in LiCl-Li2O Melt

Alloys of U with Ti are of importance in nuclear industry as fuel for Gen IV fast reactors, hydrogen isotope storage medium for fusion reactors, super conductors, and also as corrosion resistant material for use in various applications. Here, preparation of U2Ti intermetallic compound was investigated by the direct electrochemical reduction of mixed oxide of UO2-TiO2 in LiCl-0.5% Li2O molten salt at 650 °C. The mixed oxide pellet of UO2-TiO2 sintered at 1500 °C was found to be a mixture of UTi2O6 and UO2 as evidenced by X-ray diffraction (XRD) analysis. Direct electro-lithiothermic reduction of UO2, TiO2, and a mixture of sintered UO2-TiO2 and UTi2O6 coupled with cyclic voltammetry of these oxides in the melt was performed to understand the electro-reduction mechanism. Potentials of reduction of these oxides in the melt, w.r.t Ni/NiO reference electrode, obtained by analysis of CV data of these oxides contained in metallic cavity electrodes and XRD analysis of partially electro-reduced oxides were used to arrive at the electro-reduction mechanism. Results indicate that U2Ti can be prepared conveniently by the electro-lithiothermic reduction of sintered pellet of UO2-TiO2 cathode by constant current electrolysis in a two-electrode cell.

Facile synthesis of iodine variants-incorporated lithium perrhenate crystal and film: Resistive switching device and synaptic behavior

This study investigates the integration of iodine as a dopant into lithium perrhenate (LiReO4) using rhenium oxide (Re2O7) as a precursor, aiming to enhance the electrical conductivity of the compound, with implications for various material science applications. The iodine variants-incorporated LiReO4 (Iv@LiReO4·H2O) exhibits a notable improvement in the average electrical conductivity (∼ 2 S/cm) and light absorption across a broad spectrum, extending to the near-infrared range. Additionally, the doping process induces resistive switching and synaptic behaviors due to iodine diffusion. The presence of iodine and the partial reduction of Re oxide is confirmed by X-ray photoelectron spectroscopy, while UV-Vis absorption spectroscopy indicates the existence of incorporated iodine variants species. Density functional theory calculations further elucidate the mechanism by which iodine doping triggers a significant enhancement in electrical conductance, primarily by introducing a mixed-valence oxidation state in rhenium, leading to the narrowing of the band gap from 3.68 eV to 0.33 eV. This research suggests potential uses for Iv@LiReO4·H2O in applications to memristive neuromorphic devices.