Hydrogen Ion Research Articles

Time-dependent metal ionization and the persistence of collisionally excited emission lines in the diffuse ionized gas of star forming galaxies

Abstract We extend our time-dependent hydrogen ionization simulations of diffuse ionized gas to include metals important for collisional cooling and diagnostic emission lines. The combination of heating from supernovae and time-dependent collisional and photoionization from midplane OB stars produces emission line intensities (and emission line ratios) that follow the trends observed in the Milky Way and other edge-on galaxies. The long recombination times in low density gas result in persistent large volumes of ions with high ionization potentials, such as O iii and Ne iii. In particular, the vertically extended layers of Ne iii in our time-dependent simulations result in [Ne III] 15μm/[Ne II] 12μm emission line ratios in agreement with observations of the edge-on galaxy NGC 891. Simulations adopting ionization equilibrium do not allow for the persistence of ions with high ionization states and therefore cannot reproduce the observed emission lines from low density gas at high altitudes.

A meta-analytical approach for estimating methane suppression from dietary additives in ruminants

IntroductionMethane production inhibitors included in feed additives are increasingly used to suppress methane production in the rumen. Most products interact with the rumen microbiome and/or component biochemical pathways that scavenge free hydrogen ions (H+) to make methane (CH4 ). The capacity of these agents to inhibit rumen methane production is determined by the ability of the chemical to block methane production pathways, the amount of agent delivered to the rumen (i.e. the dose) and the absorption, distribution, metabolism and excretion (i.e. the pharmacokinetic) characteristics of the chemical that contribute to removal from the site of action (the rumen). The intrinsic inhibitory capacity of an agent determines the maximum rate of methane suppression. This maximal rate may reduce according to pharmacokinetic effects arising from dose rate and frequency. Most studies of additive methane reduction efficacy use total mixed ration (TMR; with the additive included into the ration) feeding systems and estimate methane reduction (absolute or relative) across a 24-hour period. Few studies report critical pharmacokinetic parameters, making it difficult to extrapolate findings into non-TMR systems (such as grazing) where differing doses and dose frequencies apply.MethodsWe consider the likely behaviour of a rumen-acting oral additive to reduce methane production applying basic pharmacokinetic principles to propose an analytical approach to data from multiple field studies employing different dose rates and dose frequencies to estimate methane suppression responses. This is based upon a logistic transformation of relative efficacy (percentage reduction in methane comparing treatment with control groups) as the dependent variable and includes total dose, dose frequency, quadratic and interaction terms between total dose and dose frequency as independent variables that potentially capture any pharmacokinetic effects on performance. The model was tested using simulation and verified against real data (cattle 3-nitrooxypropanol (3-NOP) methane-reduction studies).ResultsGood fit between predicted and observed methane suppression was obtained.DiscussionWe propose use of the general form of this logistic model with dose and dose frequency components included that address basic pharmacological impacts on methane suppression as the standard approach to meta-analysis.

Ultrahigh Concentration Hydrogen Doping into TiO2.

We investigate ultrahigh concentration doping of hydrogen (H) into rutile-TiO2 (100) single crystals by low-energy (2.5 keV) hydrogen ion beam irradiation at low temperature (LT). While the hydrogen concentration was limited to H0.3TiO2 at 300 K, in situ nuclear reaction analysis (NRA) revealed ultrahigh concentration doping of hydrogen up to H1.2TiO2 by the LT irradiation at 50 K. The large (∼8.2%) expansion of the out-of-plane lattice constant suggests that hydrogen occupies interstitial sites in rutile TiO2. Hydrogens of early stage irradiation act as electron donors and induce a large increase in conductivity, which is consistent with theoretical studies in the dilute limit. The nature of excess H was investigated in situ by transport and photoemission measurements. After LT excess H doping and postannealing to room temperature, unusual electrical transport properties were observed while maintaining the ultrahigh H concentration. In situ photoemission measurements show that the excessively doped hydrogens by LT irradiation generate a deeper in-gap state (IGS) of metastable nature. Density functional theory predicts the formation of double neighboring interstitial hydrogens as a possible mechanism for the deeper IGS.

Electrochemical Characteristics of Ambarella Peel Waste as Liquid Electrolyte for Zn-Cu Biobattery

This study focuses on the electrochemical characterization of Zn-Cu bio-battery cells utilizing electrolytes derived from ambarella peel waste. The primary objectives are to determine the half-cell and full-cell characteristics of these bio-batteries at various concentration ratios and to identify the optimal concentration ratio for maximum performance. Cyclic voltammetry analysis of the half-cells revealed an oxidation peak at 0.5 V vs Ag/AgCl, corresponding to the conversion of uronic acid to aldaric acid. Additionally, two reduction peaks were observed: hydrogen ion reduction to H2 at 0 V vs Ag/AgCl and water reduction at –0.42 V vs Ag/AgCl. The rate-determining step analysis indicated that the redox reactions in the ambarella peel electrolyte solution were surface reactions. The highest rate constant (ks) of 0.722 ± 0.05 s–1 was observed at a 1:2 concentration ratio. This ratio also resulted in the highest battery capacity of 0.0816 mAh and the maximum power density of 16.13 mW/m2. The study concluded that the 1:2 concentration ratio of ambarella peel waste electrolyte solution is optimal, outperforming the 1:1 and 1:3 ratios in terms of battery capacity and power density.

A retarded foam acid fluid system for low-temperature dolomite geothermal reservoir stimulation and its action mechanisms

Acidizing improves geothermal reservoir productivity by dissolving rocks to increase formation permeability, which is achieved by injecting acid fluids into reservoir formations. However, conventional acid fluids either can not achieve effective acidizing or cause geothermal reservoir damages. Foam acid fluids, which have been applied for oil-gas reservoir stimulation, can realize effective acidizing by retarding acid-rock reactions, and can protect reservoirs. Here, a foam acid fluid system is proposed, aiming at achieving efficient acidizing and reservoir protection in low-temperature dolomite geothermal reservoirs. Formic acid (FA) and acetic acid (HAc) are used to replace a portion of hydrochloride (HCl) acid. Alkyl glycine surfactant AGS-12 is added for foaming, while xanthan gum and nano silica particles are used to stabilize foams. Corrosion inhibitor and ferric ion stabilizer are added to inhibit acid corrosion of steel and ferric ion precipitations. The acidizing effect was evaluated through foam stability, dissolution performance, corrosion inhibition performance, and compatibility. Microscopic observation, field emission scanning electron microscope, and numerical simulation were applied to reveal the mechanisms of temporal evolution of foams and acid dissolution behaviors. Results show that the foam acid fluid with 5 wt% FA, 5 wt% HAc and 10 wt% HCl acid has the best foam stability and retardation effect. Compared to non-foam acid fluid, the decrease degree of the cuttings mass change rate in foam acid fluids exceeds 50 %, and foaming primarily retards acid-rock reactions. Simulation results is consistent with the experiment results, demonstrating that the cuttings dissolve less in FA and HAc. Calcium (Ca) content on the cuttings surfaces after acid-rock reactions in foam acid fluids with FA and HAc is less than that after acid-rock reactions in foam acid fluid with sole HCl acid, indicating that FA and HAc inhibit Ca-bearing mineral precipitations, as formate and acetate ions can chelate with Ca2+. The replacement of HCl acid by FA and HAc contributes to a low corrosivity and good compatibility of the foam acid fluids due to a reduced hydrogen ions resulted from partial dissociation of weak acids. This study shows the feasibility of foam acid fluids during geothermal reservoir stimulation with eliminated reservoir damages.

ITER-relevant 600 s steady-state extraction of negative hydrogen ions at the test facility ELISE

Abstract The neutral beam heating system for the future international fusion experiment ITER will be based on RF driven ion sources delivering a large (≈1×2 m2) and homogeneous negative hydrogen or deuterium ion beam of several ten Amperes over up to several hundred seconds. The size scaling experiment ELISE (Extraction from a Large Ion Source Experiment) is an integral part of the R&D road-map towards the ITER neutral beam heating system. Recently, 90 % of the ITER target for the extracted current density was achieved in hydrogen for 600 s, increasing the pulse length over that such current densities are possible by a factor of more than ten. For ten second beam pulses the ITER target current density was achieved. These breakthrough results are made possible by a steady-state capable HV power supply together with an improved version of internal potential rods and a modified topology of the magnetic filter field.

Mechanism of ion migration from the substrate material into snow cover at the end of the cold period

Earlier, it was established that maximum mineralization of the contact layer of snow occurs in spring at the interface with substrates (soil or ice). This study analyzes the temperature and moisture conditions during this period at the interface of the contact layer of snow with substrates by examining frozen sand blocks saturated with a solution containing complex gold ions, or blocks filled with polystyrene containing ions of molybdenum, copper, etc. It is assumed that the migration of ions from the underlying substrate into the contact layer of snow cover in spring occurs along quasi-liquid films on the surface of snow crystals, the thickness of which exceeds the equilibrium one. Migration becomes noticeable when the temperature at the snow–substrate contact reaches −13 °С and above. The appearance of quasi-liquid films on the surface of snow particles under variable temperature and moisture conditions is possible due to the condensation of water vapor, which during the day, with general heating of the system, can enter the contact layer of snow both from above and below. With an increase in snow density in the spring, the mineralization of the near-contact layer of snow cover increases. At the same time, linear relationships were revealed between the content of substrate components migrating into the near-contact layer of snow and the gradient of water vapor density in it. The reliability of the approximation of these dependencies for the gold thiosulfate complex is 0.98; for copper ions – 0.52; for hydrogen ions – 0.88; for sodium ions – 0.69, for chloride anions – 0.89. The results of the study substantiate the increased efficiency of geochemical prospecting for mineral deposits using snow cover in the spring.

ProtonationDriven Polarization Retention Failure in Nano-Columnar Lead-Free Ferroelectric Thin Films.

Understanding microscopic mechanisms of polarization retention characteristics in ferroelectric thin films is of great significance for exploring unusual physical phenomena inaccessible in the bulk counterparts and for realizing thin-film-based functional electronic devices. Perovskite (K,Na)NbO3 is an excellent class of lead-free ferroelectric oxides attracting tremendous interest thanks to its potential applications to nonvolatile memory and eco-friendly energy harvester/storage. Nonetheless, in-depth investigation of ferroelectric properties of (K,Na)NbO3 films and the following developments of nano-devices are limited due to challenging thin-film fabrication associated with nonstoichiometry by volatile K and Na atoms. Herein, ferroelectric (K,Na)NbO3 films of which the atomic-level geometrical structures strongly depend on thickness-dependent strain relaxation are epitaxially grown. Nanopillar crystal structures are identified in fully relaxed (K,Na)NbO3 films to the bulk states representing a continuous reduction of switchable polarization under air environments, that is, polarization retention failures. Protonation by water dissociation is responsible for the humidity-induced retention loss in nano-columnar (K,Na)NbO3 films. The protonation-driven polarization retention failure originates from domain wall pinning by the accumulation of mobile hydrogen ions at charged domain walls for effective screening of polarization-bound charges. Conceptually, the results will be utilized for rational design to advanced energy materials such as photo-catalysts enabling ferroelectric tuning of water splitting.

A public grid of radiative transfer simulations for Lyα and metal lines in idealised galactic outflows

The vast majority of star-forming galaxies are surrounded by large reservoirs of gas ejected from the interstellar medium. Ultraviolet absorption and emission lines represent powerful diagnostics to constrain the cool phase of these outflows, through resonant transitions of hydrogen and metal ions. The interpretation of these observations is often remarkably difficult as it requires detailed modelling of the propagation of the continuum and emission lines in the gas. To this aim, we present a large public grid of ≈20 000 simulated spectra that includes H I Lyα and five metal transitions associated with Mg II, C II, Si II, and Fe II which is accessible online. The spectra have been computed with the RASCAS Monte Carlo radiative transfer code for 5760 idealised spherically symmetric configurations surrounding a central point source emission, and characterised by their column density, Doppler parameter, dust opacity, wind velocity, as well as various density and velocity gradients. Designed to predict and interpret Lyα and metal line profiles, our grid exhibits a wide diversity of resonant absorption and emission features, as well as fluorescent lines. We illustrate how it can help better constrain the wind properties by performing a joint modelling of observed Lyα, C II, and Si II spectra. Using CLOUDY simulations and virial scaling relations, we also show that Lyα is expected to be a faithful tracer of the gas at T ≈ 104 − 105 K, even if the medium is highly ionised. While C II is found to probe the same range of temperatures as Lyα, other metal lines merely trace cooler phases (T ≈ 104 K). As their gas opacity strongly depends on gas temperature, incident radiation field, metallicity and dust depletion, we caution that optically thin metal lines do not necessarily originate from low H I column densities and may not accurately probe Lyman continuum leakage.

Guidance on aqueous matrices for evaluating novel precipitants and adsorbents for phosphorus removal and recovery

Phosphorus (P) removal from water and recovery into useable forms is a critical component of creating a sustainable P cycle, although mature technologies for P removal and recovery are still lacking. The goal of this paper was to advance the testing of novel materials for P removal and recovery from water by providing guidance on the development of more realistic aqueous matrices used during materials development. Literature reports of “new” materials to remove P from water are often difficult to compare in terms of performance because authors use a myriad of water chemistries containing P concentrations, pH, and competing ions. Moreover, many tests are conducted in simplified matrices that do not reflect conditions in real systems. To address this critical gap, the research herein developed a systematic approach of identifying aqueous matrices relevant to P recovery, including key components in the aqueous matrices having the greatest influence on the mechanisms of P removal with emphasis on phosphate precipitation and phosphate adsorption, and providing guidelines on relevant “recipes” for aqueous solutions for testing novel materials. Key components in the aqueous matrices included hydrogen ion (i.e., pH), multivalent metal cations, and dissolved organic matter due to their influence on phosphate precipitation and adsorption mechanisms. Recipes for buffer solution and synthetic groundwater, surface water, anaerobic digestate, and stored urine are discussed in the context of P removal and recovery processes. Wherein the adoption of standard matrices in other fields have permitted direct comparison of processes or materials, it is anticipated that adoption of relevant aqueous matrix recipes for P removal and recovery will improve the ability to directly compare novel materials and processes.

Numerical investigation into the acid flow and reaction behavior in the tight, naturally fractured carbonate reservoir during acid fracturing

Tight naturally fractured carbonate reservoirs require acid fracturing to build the connectivity between the wellbore and natural fractures (NFs), where hydrocarbon is stored. The high leakoff nature of the NF complicates the acid flow and etching pattern, raising the difficulty in acid fracturing design and optimization. To explore the acid flow and reaction behavior in such reservoirs, an acid fracturing model accounting for the NF distribution is developed, which consists of a fracture surface characterization model, a fracture propagation model, and an acid-etching model. Based on the model, the effects of injection parameters and the NF properties on the effectiveness of acid fracturing are investigated. Then, strategies for acid fracturing the tight naturally fractured carbonate reservoirs are proposed. Results show that high pumping rates and retarded acids with low hydrogen ion (H+) diffusion coefficient is conducive to achieving a long acid penetration distance, while a low pumping rate and acids with a high H+ diffusion coefficient facilitates the NF etching. Therefore, a large stimulated area can be achieved by applying a multi-stage alternating injection of the crosslinked acid with a high pumping rate followed by the gelled acid with a low injection rate. NFs impact acid fracturing in two distinct ways: enhancing the non-uniform etching of the fracture surface and reducing the effective acid-etched fracture length through high leakoff. When NF density is high, leakoff control techniques should be employed; and when the NF inclination is high, non-uniform etching techniques should be used to generate acid-etched channels in flow barriers.

Construction of acidic microenvironment by Cu-TCPP nanozyme composited deprotonatable polymeric nanofibers for efficient antibacterial activity

The issue of bacterial resistance caused by conventional antibiotics has emerged as a major challenge in clinical treatment. Nanozymes, based on catalysis and devoid of bacterial resistance, provide a novel approach to eradicating bacteria. However, the practical potential of these nanozymes is limited by their low and readily pH-affected catalytic activity. Herein, the enzyme activity was optimized starting from the synthesis of nanozyme and the selection of carboxylate-containing polymers for the matrix. Specifically, various copper-tetrakis (4-carboxyphenyl) porphyrin (Cu-TCPP) were initially synthesized employing three copper sources, and among them, Cu-TCPP derived from Cu2O with higher catalytic activity was preferred. Subsequently, Cu-TCPP composite fibrous membranes were further obtained by electrospinning from their blend solutions with different polymers with distinct deprotonation capabilities. Thus, an acidic microenvironment conducive to the exertion of enzyme activity was constructed. The fabricated composite nanofibrous membrane could dissociate hydrogen ions to construct a localized acidic microenvironment even under weakly alkaline conditions, thereby enhancing the enzyme activity and improving the antibacterial effect. Further in vivo experiments demonstrated its favorable antibacterial ability and accelerated wound healing effect. The enhancement strategy of enzyme activity in this study brings inspiration for the design of nanozyme composited wound dressings and holds significant potential for clinical antibacterial applications

Insights into heat treatments of biodegradable Mg-Y-Nd-Zr alloys in clinical settings: Unveiling roles of β' and β1 nanophases and latent in vivo hydrogen evolution

Heat treatment serves as a viable strategy to effectively mitigate the intense corrosion of biodegradable WE43 alloys. However, limited comprehension of the passivation mechanisms underlying heat treatment and the dilemma to quantitatively examine the evolution of hydrogen gas in vivo introduce uncertainties in designing heat treatments for developing clinically applicable WE43. This work aims to advance this knowledge by applying cutting-edge atom probe tomography to provide atomic-scale insights into the passivation roles of rare earth (RE)-rich β1 (Mg3(Y, Nd)) and β' (Mg12NdY) nanophases induced by T6 heat treatment at 250 °C, and employing machine learning-based image analysis techniques to quantitatively unveil WE43’s in vivo gas evolution during a 12-week implantation. It was found that nanosized β1 and β' phases can effectively improve WE43′s corrosion resistance by inducing an accelerated passivation effect on the surface and confining the distribution of hydrogen ions in the matrix. Female rats presented slightly higher corrosion rates than male rats in weeks 1 and 4 but lower hydrogen gas volumes in vivo, while male rats possessed a superior ability to metabolise hydrogen gas in vivo. Notably, latent gas evolution against the corrosion rates was found which peaked at week 4 and subsided at week 12 despite the gradually decreased corrosion rates from week 1 to 12. This study offers insights for engineering heat treatments to develop clinically applicable WE43 with acceptable corrosion rates and in vivo gas generation at various implantation stages. Statement of SignificanceThe study aimed to reveal the role of β1 and β' nanophases on the good corrosion resistance of WE43. The influence of these nanophases on WE43′s corrosion performance has not been totally understood. Similarly, the understanding of hydrogen gas evolution as it relates to the magnesium implant's corrosion rate lacks clarity. Atom probe tomography (APT) indicates β1 and β' nanophases trap hydrogen, removing H2 from the lattice and disabling its catalytic role in Mg oxidation. Machine learning-aided analyses of computed tomography (CT) scan images indicate latent gas evolution, contradicting the monotonic in vivo H2 evolution that is widely accepted.

Effect of Beta-Alanine Supplementation on Maximal Intensity Exercise in Trained Young Male Individuals: A Systematic Review and Meta-Analysis.

Beta-alanine is a nonessential amino acid that is commonly used to improve exercise performance. It could influence the buffering of hydrogen ions produced during intense exercise and delay fatigue, providing a substrate for increased synthesis of intramuscular carnosine. This systematic review evaluates the effects of beta-alanine supplementation on maximal intensity exercise in trained, young, male individuals. Six databases were searched on August 10, 2023, to identify randomized, double-blinded, placebo-controlled trials investigating the effect of chronic beta-alanine supplementation in trained male individuals with an age range of 18-40years. Studies evaluating exercise performance through maximal or supramaximal intensity efforts falling within the 0.5-10min duration were included. A total of 18 individual studies were analyzed, employing 18 exercise test protocols and 15 outcome measures in 331 participants. A significant (p = .01) result was observed with an overall effect size of 0.39 (95% confidence interval [CI] [0.09, 0.69]), in favor of beta-alanine supplementation versus placebo. Results indicate significant effects at 4weeks of supplementation, effect size 0.34 (95% CI [0.02, 0.67], p = .04); 4-10min of maximal effort, effect size 0.55 (95% CI [0.07, 1.04], p = .03); and a high beta-alanine dosage of 5.6-6.4g per day, effect size 0.35 (95% CI [0.09, 0.62], p = .009). The results provide insights into which exercise modality will benefit the most, and which dosage protocols and durations stand to provide the greatest ergogenic effects. This may be used to inform further research, and professional or recreational training design, and optimization of supplementation strategies.

Comprehensive research facility for negative ion source neutral beam injection at CRAFT: design and first operations

Abstract Neutral beam injection (NBI) has been proven as a reliable heating and current drive method for fusion plasma. For the high-energy NBI system (particle energy > 150 keV) of large-scale fusion devices, the negative ion source neutral beam injection (NNBI) system is inevitable, which can obtain an acceptable neutralization efficiency (> 55%). But the NNBI system is very complex and challengeable. To explore and master the key NNBI technology for future fusion reactor in China, an NNBI test facility is under development in the framework of the Comprehensive Research Facility for Fusion Technology (CRAFT). The initial goal of CRAFT NNBI facility is to achieve a 2 MW hydrogen neutral beam at the energy of 200–400 keV for lasting 100 s. In the first operations of the CRAFT NNBI facility, a negative ion source with dual RF drivers was developed and tested. By using the 50 keV accelerator, the long-pulse and high-current extractions of negative hydrogen ions have been achieved and the typical values were 55.4 keV, 7.3 A (~ 123 A/m2), 105 s and 55.0 keV, 14.7 A (~ 248 A/m2), 30 s, respectively. By using the 200 keV accelerator, the megawatt-class negative hydrogen beam has also been achieved (135.9 keV, 8.9 A, 8 s). The whole process of the gas neutralization of negative ion beam, electric removal of residual ions, and beam transport have been demonstrated experimentally.

Generalised hydrogen interactions with CINCO: a window to new physics

We present semi-analytic solutions for atomic transition rates in hydrogenic atoms induced by scalar, pseudoscalar, vector, axial-vector, and tensor interactions. Our results agree with quantum electrodynamics predictions to ~ 0.005 % precision, and further allow us to calculate absorption and emission rates for axions, hidden photons, light scalars or other dark matter candidates for hydrogen and hydrogenic ions. These results can be used to inform searches for light new physics as well as in calculations relevant to searches for fifth forces or varying fundamental constants, with applications from astrophysics to laboratory spectroscopy experiments. We also provide a dedicated tool for the construction of hydrogenic transition amplitudes: “Computation of hydrogen radial INtegrals and COefficients” (CINCO).

Long-term effects of wildfires on river water quality: a comprehensive review of the variability of water quality in South Korea

ABSTRACT After wildfires, the loss of the humus layer leads to increased runoff and ash-related pollutants entering rivers. This study examined the long-term effects of wildfires on river water quality, focusing on 7 years before and after the wildfire events. We statistically analyzed the changes in the water quality of streams surrounding the wildfire area following a major wildfire. We used eight water quality parameters provided by the National Institute of Environmental Research for the analysis. To assess the impact of the wildfires, we employed t-tests and point-biserial correlation analysis to compare the changes in water quality indicators before and after the wildfires. Additionally, an analysis of variance was conducted to evaluate the impact of three wildfires, each occurring in different periods, on the water quality in a single river basin. The results showed increasing trends in hydrogen ion concentration (pH), electrical conductivity, and dissolved oxygen after the wildfire, whereas biochemical oxygen demand, total phosphorus, and total nitrogen exhibited decreasing trends. The impact of wildfires on changes in suspended solids was relatively minimal. It is expected that the results of this study provide valuable insights into developing water quality management and restoration plans following wildfires.

Excess Energy Released Due To Proton-Proton Collisions in Condensed Matter Could Be Due To Laboratory-Made Micro Black Holes

While sodium metal dissolution in concentrated (2M) Epsom solution is very peaceful under stirring conditions in about 5 to 10s, its dissolution in a dilute (0.85) Epsom solution has turned very violent. Nearly 30s after the addition of Na, the solution exploded accompanied by the vaporization of the glass beaker. Only sodium aerosol and tiny molten needles of glass were seen around indicating a very high temperature (>1000 0C) has indeed been reached. The timing of the explosion has indicated that hydrogen released during sodium dissolution has got trapped in the salt solution and subsequent energy build-up has caused the excess energy release. A viable trapping mechanism involving the exchange of 2 hydrogen ions (H22+) with an Mg2+ ion in cavitation-induced nanocrystals of Epsom has been proposed in this regard. The two hydrogen ions are stabilized at the cation vacancy (cavity) by dative bonds with the two hydrogen ions in the water molecule trapped at a neighboring sulphate vacancy. Spring-like action between the two protons trapped at the cation vacancy due to oscillations caused by two opposing forces – one by cavitation and the other by coulombic repulsion eventually appear to have led to the collision of hydrogen ions at relativistic speeds in condensed matter. To start with, the two protons in the H22+ species are confined in a small space (72 pm cavity) at a single crystal cation lattice site in Na2SO4 nanocrystal which increases their head-on collision probability at high energies. There is no upper limit to the energies achieved through p-p collisions in this species as the Cavitation-Coulombic Repulsion Oscillations (CCRO) can continue until the endpoint is reached. Regeneration of a nanocrystal over a sufficiently small time scale and regeneration effect prior to cavitation collapse are all important so laws of thermodynamics are not violated. Extra dimensions of gravity at short distances, if present, could also assist in the high energies required for the production of mini black holes in condensed matter. Such black holes lose mass very quickly through the emission of Hawking radiation observed in the form of explosion with mass-energy equivalence of E = mc2. The possibility of tapping such explosive energy for peaceful purposes is discussed. As such it constitutes the third kind of atomic energy humans have entertained, the first two being fission and fusion.

Electronic Descriptor to Identify the Activity of SACs for E-NRR and Effect of BF3 as Electrolyte Ion.

Electrochemical nitrogen reduction reaction (e-NRR) is an eco-friendly alternative approach to generate ammonia under ambient conditions, with very low power supply. But, developing of an efficient catalyst by suppressing parallel hydrogen evolution reaction as well as avoiding the catalysts poisoning either by hydrogen or electrolyte ion is an open question. So, in order to screen the single atom catalysts (SACs) for the e-NRR, we proposed a descriptor-based approach using density functional theory (DFT) based calculations. We investigated total 24 different SACs of types TM-Pc, TM-N3C1, TM-N2C2, TM-NC3 and TM-N4, considering transition metal (TM). We have considered mainly BF3 ion to understand the role of electrolyte and extended the study for four more electrolyte ions, Cl, ClO4, SO4, OH. Herein, to predict catalytic activity for a given catalyst we have tested 16 different electronic parameters. Out of those, electronic parameter dxz↓ occupancy, identified as electronic descriptor, is showing an excellent linear correlation with catalytic activity (R2=0.86). Furthermore, the selectivity of e-NRR over HER is defined by using an energy parameter ▵G*H-▵G*NNH. Further, the electronic descriptor (dxz↓ occupancy) can be used to predict promising catalysts for e-NRR, thus reducing the efforts on designing future single atom catalysts (SACs).

Efficacy of zinc and copper oxide nanoparticles as heat and corrosion-resistant pigments in paint formulations

This study focuses on the synthesis of zinc and copper oxide nanoparticles using green methods by plant extracts. The resulting metal oxides were analyzed using FT-IR spectroscopy, TGA, TEM, zeta potential and assessed for their efficacy as pigments based on properties such as Hydrogen Ion Concentration, Oil absorption, Moisture Content, Fineness of grinding, Bleeding, and loss on ignition. The results confirmed that the prepared ZnO and CuO nanoparticles exhibited the formation of nanoparticles in the range of 10–40 nm with potential as pigments. Two paint formulations incorporating these nanoparticles and silicon resins as binders were tested for physico-mechanical attributes, chemical resistance, heat resistance, and corrosion resistance of the dry paint films. The study found that the films containing the prepared oxides demonstrated excellent performance, with no damage or color alteration observed after exposure to temperatures up to 500 °C. Moreover, the paint films containing ZnO nanoparticles showed superior efficiency after a 500 h salt spray test compared to those with CuO nanoparticles. These findings suggest that the synthesized mixed oxide nanoparticles are promising candidates for heat-resistant pigment applications.