Effect Of Water Vapor Research Articles

Effect of water vapor on fining and viscosity of soda-lime glass melts

Effect of water vapor on fining and viscosity of soda-lime glass melts

Enhancement of removing OH bonds from low-temperature deposited silicon oxide films by adding water vapor into NH3 gas annealing at 130 oC

Abstract It was found that annealing with water-vapor-added NH3 gas (water-added NH3) is more effective than with dry NH3 at removing residual OH bonds in silicon oxide (SiOx) films deposited by atmospheric chemical vapor deposition with an organic silicon source. Fourier transform infrared spectra showed that reduction amount of OH bonds using the water-added NH3 was ~4 or ~1.3 times larger than using the conventional dry N2 or dry NH3 mixed with N2 gas without water, respectively. This result is something strange because water can be a potential candidate of OH sources. The effect of water vapor on OH-bond removal can be explained by considering following three factors. One is that low-temperature SiOx films are constrained somewhat, the second is that strained Si-O-Si bonds are in higher or more unstable energy state than strain-free ones, and the third is that highly strained bonds are easily hydroxylated to form Si-OH bonds.

Electrochemical Migration Study on Sn-58Bi Lead-Free Solder Alloy Under Dust Contamination.

With the development of electronic packaging technology toward miniaturization, integration, and high reliability, the diameter and pitch of solder joints continue to shrink. Adjacent solder joints are highly susceptible to electrochemical migration (ECM) due to the synergistic effects of high-density electric fields, water vapor, and contaminants. Dust has become one of the non-negligible causal factors in ECM studies due to air pollution. In this study, 0.2 mM/L NaCl and Na2SO4 solutions were used to simulate soluble salt in dust, and the failure mechanism of an Sn-58Bi solder ECM in the soluble salt in dust was analyzed by a water-droplet experimental method. It was shown that the mean failure time of the ECM of an Sn-58Bi solder in an NaCl solution (53 s) was longer than that in an Na2SO4 solution (32 s) due to the difference in the anodic dissolution characteristics in the two soluble salt solutions. XPS analysis revealed that the dendrites produced by the ECM process were mainly composed of Sn, SnO, and SnO2, and there were precipitation products-Sn(OH)2 and Na2SO4-attached to the dendrites. The corrosion potential in the NaCl solution (-0.351 V) was higher than that in the Na2SO4 solution (-0.360 V), as shown by a polarization test, indicating that the Sn-58Bi solder had better corrosion resistance in the NaCl solution. Therefore, an Sn-58Bi solder has better resistance to electrochemical migration in an NaCl solution compared to an Na2SO4 solution.

Impact of water vapor on the 2D MoS2 growth in metal-organic chemical vapor deposition

In the presented work, the method of metal–organic chemical vapor deposition (MOCVD) using Mo(CO)6 and H2S assisted by oxidative etching with water vapor, was employed for the synthesis of MoS2. This study was aimed at detailed investigation of the films' properties obtained via this method and identifying methods for elimination of such disadvantages as the carbon impurities and the small size of crystalline domains in the films. It was found that in the temperature range from 850 °C to 950 °C, the effect of water vapor on the morphology of MoS2 is significantly different. The study of the chemical states of molybdenum and sulfur made it possible to associate the size of the crystal domains formed with the efficiency of removing the oxidized states of Mo6+ and S6+. It is assumed that the increase in the domains’ size is due to rapid lateral growth, resulting from the complete removal of the oxidized states at the edges, as well as a decrease in the density of nucleation centers due to the etching of less stable seeds on the substrate surface.

Influences of reformate on the performance of high temperature proton exchange membrane fuel cell and its optimization strategy

Due to the challenges of hydrogen production, storage and transport, hydrocarbon reformate-based high temperature proton exchange membrane fuel cell (HT-PEMFC) has wide application opportunities. However, the inevitable water vapor and CO in reformate significantly determines the fuel cell performance and durability. In this work, a three-dimensional, non-isothermal and multiphase model based on agglomerate sub-model is developed to investigate the effects of reformate components and operating conditions, in which multiphase transport, dissolution, diffusion, adsorption, desorption and reaction of H2 and CO are considered. The results show that the fuel cell performance increases with the rising of water vapor content as CO content higher than 2 % (dry basis, the same below) and water vapor content lower 20 % (wet basis). The alleviation effect of water vapor on CO poisoning is discovered due to reduced CO coverage rather than enhanced CO electrochemical oxidation. An elevated temperature leads to improved performance and the effect of CO poisoning (CO<3%) is weak at 180°C.

Understanding the influences and mechanism of water vapor on CO2 capture by high-temperature Li4SiO4 sorbents

Li4SiO4 sorbent attracts wide attention due to its high and stable CO2 adsorption. However, the process of CO2 capture is significantly affected by various impurities under the circumstance of industrial applications, and water vapor is one such impurity that needs to be well studied. Herein, we aim to evaluate the effect of water vapor on physicochemical characteristics of Li4SiO4-based sorbents during cyclic CO2 adsorption and desorption and to understand the action mechanism of H2O molecules on CO2 adsorption by Li4SiO4. Reaction tests show that water vapor can significantly enhance CO2 adsorption performance of sorbents, but the promotion effect varies with the different presence of water vapor during reactions. Material characterization and DFT calculation reveal that although the presence of water vapor leads to deterioration of internal pore structure of the sorbent, H2O molecule will form OH– on the surface of Li4SiO4 and further react with CO2 to generate HCO3–, thus the adsorption energy with water vapor presenting is increased with an observation of promoted CO2 adsorption.

The effect of water vapour and sulfur on the methane combustion reaction on Pd13 clusters: Insights from a first principles study

Catalytic methane combustion represents a highly efficient and environmentally-friendly approach, which can significantly reduce methane emissions in coal mines. However, the presence of water vapor and sulfides in coal mine methane exhaust gas can lead to catalyst poisoning deactivation. This article employs density functional theory calculations based on the GGA-PBE method to investigate the effects of water vapor and sulfur on methane combustion on Pd13 clusters. According to thermodynamic parameters, we have determined the optimal reaction pathway for CH4 decomposition as CH4* → CH3* → CH2* → CH* → CHO*, while the optimal reaction pathway for CO2 formation is CH* → CHO* →CO* → CO2*. Additionally, water vapor generates additional OH* radicals, which lower the adsorption energy of CH4 on Pd13 clusters and alter the reaction pathway for methane oxidation, inhibiting the catalytic oxidation of CH4. Sulfides occupy the active sites on the catalyst surface, leading to a decrease in the activity of methane oxidation. These findings deepen our understanding of the mechanisms by which palladium-based catalysts catalyze methane combustion. Based on these findings, we have also proposed strategies for water and sulfur resistance of the catalyst, providing guidance for the future development of water-resistant and sulfur-resistant CH4 catalytic combustion catalysts.

The Evaluation of Rainfall Forecasting in a Global Navigation Satellite System-Assisted Numerical Weather Prediction Model

Accurate water vapor information is crucial for improving the quality of numerical weather forecasting. Previous studies have incorporated tropospheric water vapor data obtained from a global navigation satellite system (GNSS) into numerical weather models to enhance the accuracy and reliability of rainfall forecasts. However, research on evaluating forecast accuracy for different rainfall levels and the development of corresponding forecasting platforms is lacking. This study develops and establishes a rainfall forecasting platform supported by the GNSS-assisted weather research and forecasting (WRF) model, quantitatively assessing the effect of GNSS precipitable water vapor (PWV) on the accuracy of WRF model forecasts for light rain (LR), moderate rain (MR), heavy rain (HR), and torrential rain (TR). Three schemes are designed and tested using data from seven ground meteorological stations in Xi’an City, China, in 2021. The results show that assimilating GNSS PWV significantly improves the forecast accuracy of the WRF model for different rainfall levels, with the root mean square error (RMSE) improvement rates of 8%, 15%, 19%, and 25% for LR, MR, HR, and TR, respectively. Additionally, the RMSE of rainfall forecasts demonstrates a decreasing trend with increasing magnitudes of assimilated PWV, particularly effective in the range of [50, 55) mm where the lowest RMSE is 3.58 mm. Moreover, GNSS-assisted numerical weather model shows improvements in statistical forecasting indexes such as probability of detection (POD), false alarm rate (FAR), threat score (TS), and equitable threat score (ETS) across all rainfall intensities, with notable improvements in the forecasts of HR and TR. These results confirm the high precision, visualization capabilities, and robustness of the developed rainfall forecasting platform.

Characteristics and Simulation of Icing Thickness of Overhead Transmission Lines across Various Micro-Terrains

The hazard of ice accretion on overhead power circuits is significant, yet predicting it is very difficult. The key reason lies in the shortage of sufficient observational data on ice thickness, and previous studies have also rarely taken into account micro-terrain and micro-meteorological conditions. In response to the challenge of simulating overhead line icing, this study introduces a new icing simulation technique that fully considers the effects of micro-terrain and micro-meteorology. For this technique, typical micro-terrains of overhead line areas are first identified by using high-resolution elevation data, and the icing thickness characteristics in different micro-terrains are analyzed. Subsequently, icing thickness simulations for different micro-terrains are conducted. The results indicate that during the icing process, the icing thickness ranges from 5 mm to 8 mm under three types of micro-terrain, namely, “uplift type”, “alpine drainage divide type” and “canyon wind channel type”, whereas the icing thickness is less than 5 mm in the “flat type” of micro-terrain. This finding suggests that the first three micro-terrain types facilitate icing on overhead transmission lines due to the condensation and uplifting effects of water vapor caused by terrain. However, flat terrain lacks the conditions necessary for water vapor accumulation and thus is not easy to form icing. The results are advantageous for the deployment of overhead power lines in intricate terrain. It is advisable to steer clear of regions susceptible to icing, and endeavor to install circuits in level territories whenever feasible. In addition, the simulated icing thickness under different terrains is in good agreement with the observations. Specifically, the correlation coefficient between simulated and observed icing thickness is significant at the 0.99 confidence level, and the deviations between them are within 0.5 mm. This signifies that the forecasting methodologies employed are dependable and possess significant implications as a reference for disaster prevention and mitigation efforts.

Extraction evolutionary features of continuous light-induced plasmonic nanobubbles by a dynamic spectral regression model

A comprehensive understanding of the nature of light-induced plasmonic nanobubbles (PNBs) generated around noble metal nanoparticles is essential for optimizing PNB-based applications, such as light-driven microfluidic control. To investigate the overall evolution pattern of plasmonic nanobubbles (PNBs) under continuous light illumination, a computational model based on the least-squares method is established. Meanwhile, the variations in nanofluid transmittance and vaporization mass under continuous light illumination are measured by an immersion fiber and an electronic balance, respectively. The effects of nanoparticle concentration on the nanofluid transmittance and vaporization mass are analyzed. Considering the variations in nanofluid concentration, the overall evolution pattern of PNBs is preliminarily analyzed by monitoring the real-time dynamic change in nanofluid transmittance. The experimental results indicate that the nanoparticle concentration has an important effect on the nanofluid vaporization process. During the illumination stage, an increased nanofluid concentration intensifies the synergistic effect of water vaporization and PNB growth on transmittance reduction. The change in nanofluid transmittance caused by PNB scattering greatly exceeds that caused by increasing nanoparticle concentration. The nanofluid concentration gradually increases and peaks at the end of the cooling stage, and the rate of change of the nanofluid concentration is proportional to the nanofluid concentration. The numerical calculations show that the average size and the range of the PNB size distribution continuously increase with increasing irradiation time, and decrease during the cooling stage. A higher nanofluid concentration corresponds to a wider range of PNB size distribution.

Influence of Water Vapor on the Oxidation of Pure Titanium

Titanium and titanium alloys are extensively used in the aerospace, automotive, and medical industries due to their high chemical and mechanical stability. In a previous study, the influence of water vapor on the growth of the oxide scale and the formation of the oxygen diffusion zone (ODZ) for Ti-6Al-4V was investigated using a 6-zone furnace. To elucidate the effect of water vapor on the oxide scale growth and ODZ, without the effect of alloying elements on diffusion, a systematic comparative study at 500, 600, and 700 °C for up to 500 h was carried out on pure Ti. Inert marker experiments showed that outward scale growth and diffusion of Ti4+ were promoted by water vapor. Additionally, the extent of oxygen enrichment in the subsurface zone (ODZ) as a function of temperature and time was determined for pure Ti by nanoindentation profiles and compared with results obtained for Ti-6Al-4V. The thickness of the ODZ increased with increasing temperature and time for dry air and humid air. The diffusion of oxygen ions within pure Ti and Ti-6Al-4V was not significantly affected by the presence of water vapor in the oxidizing environment. The effect of water vapor on the oxide scale spallation was found to be less critical for pure Ti when compared to Ti-6Al-4V.

Synergistic Effect of Laser, Water Vapor, and Electron-Beam on the Degradation of Quasi-Two-Dimensional Ruddlesden-Popper Perovskite Flakes.

Understanding the effects of laser light, water vapor, and energetic electron irradiation on the intrinsic properties of perovskites is important in the development of perovskite-based solar cells. Various phase transition and degradation processes have been reported when these agents interact with perovskites separately. However, detailed studies of their synergistic effects are still missing. In this work, the synergistic effect of three factors (exposure to laser light, water vapor, and e-beam) on the optical and physical properties of two-dimensional (2D) Ruddlesden-Popper (RP) perovskite flakes [(BA)2(MA)2Pb3Br10] has been investigated in an environmental cell. When the perovskite flakes were subjected to moderate laser irradiation in a humid environment after prior e-beam irradiation, the photoluminescence (PL) peak centered at 480 nm vanished, while a new PL peak centered at 525 nm emerged, grew, and then quenched. This indicates the degradation process of the 2D RP perovskite was a phase transition to a three-dimensional (3D) perovskite [MAPbBr3] followed by the degradation of 3D perovskite. The spatial distribution of the 525 nm PL signal shows that this phase-transition process spreads across the flake to the area as far as ∼40 μm from the laser spot. Without humidity, the phase transition happened in the laser-irritated area but did not spread, which suggests that moisture enhanced the ion migration from the laser-scanned area to the rest of the flake and accelerated the phase transition in the nearby area. Experiments with no prior e-beam irradiation show that e-beam irradiation is the key to activating the 2D-3D phase transition. Therefore, when the three factors work synergistically, a conversion from the 2D RP perovskite into the 3D perovskite is not localized and propagates through the perovskite. These findings contribute to our understanding of the complex interactions between external stimuli and perovskite materials, thereby advancing the development of efficient and stable perovskite-based solar cells.

The Influence of Space Traffic on AIM/CIPS PMC Frequencies at 80°N

AbstractWe explore the effects of lower thermospheric water vapor deposited by launch vehicle plumes on polar mesospheric cloud (PMC) frequencies at 80°N. We use July‐averaged PMC frequencies from 2007 to 2022 from the Cloud Imaging and Particle Size (CIPS) instrument on NASA's Aeronomy of Ice in the Mesosphere (AIM) satellite. Launch sites worldwide are typically located near northern mid‐latitudes. Using the orbital launch record for the same time period, we find that the number of launches correlates with PMC frequencies with a coefficient of r = 0.60, which increases to r = 0.75 when only selecting launches from 2.5 to 21.5 local time (LT), indicating a weak LT dependence on global‐scale transport to 80°N. To support our findings, we use meridional winds from the Michelson Interferometer for Global High‐resolution Imaging experiment on NASA's Ionospheric Connection Explorer satellite and winds from the Horizontal Wind Model climatology to interpret the northward motion of air parcels at 105 km. We find the launch LT window that maximizes the correlation coefficient to be consistent with the expected maximum northward motion from the diurnal variation of mid‐latitude meridional winds. Comparisons with Microwave Limb Sounder satellite observations of upper mesospheric temperature and water vapor reveal a strong dependence of cloud frequency on water vapor (r = 0.86) but not on temperature (r = −0.26), indicating that water vapor is the primary source of PMC variability for the bright PMCs at 80°N. We therefore find that launch vehicle plumes originating primarily from northern mid‐latitudes modulate PMC frequency at 80°N in July.

Investigation of spectral bands and sensor parameters for methane emission detection imaging spectrometer

Recently, interest has increased in developing remote sensing (RS) sensor systems with a high spatial and spectral resolution for quantifying methane (CH4) emissions from point sources. Evaluating sensor parameters can lead to a better understanding of technological advancements in CH4 emission estimation. This study addresses several important topics, including the robust algorithm for point source CH4 emission detection, selecting optimum CH4 absorption bands and their sensitivity analysis, and evaluating sensor parameters such as spatial and spectral resolution and signal-to-noise ratio (SNR). Since the matched filter algorithm efficiently detects point source emissions with palpable accuracy, it has been used here for the Airborne Visible InfraRed Imaging Spectrometer – Next Generation (AVIRIS-NG) sensor data acquired over the USA. The optimum band selection for CH4 detection was determined using a normalized sensitivity method to investigate the effects of aerosol, water vapor (WV), and surface albedo variations. The impact of these parameters on the CH4 absorption bands in the short-wave infrared (SWIR) range has been analyzed using MODerate resolution atmospheric TRANsmission (MODTRAN) radiative transfer (RT) model simulations. Using AVIRIS-NG data as a testbed, various methods have been used to reconstruct original data and generate data sets with different sensor specifications. The effects of the sensor parameters, such as spatial and spectral resolution and SNR, on the detection accuracy were analyzed. The results show the significance of SNR over the spatial and spectral resolution for better emission detection. It indicates the reasonable selection of sensor parameters that can help to create an optimal sensor system that will ultimately support the development of an imaging spectrometer suitable for CH4 emission estimation.

Experimental and DFT study of Na4SiO4 doped with oxysalts for high-temperature CO2 capture

Eutectic doping has been considered as one of the most efficient ways to modify the Na4SiO4-based CO2 sorbent. Nevertheless, the effects of different acid radical ions and alkali metal cations of the oxysalts on the CO2 capture performances of Na4SiO4 have never been explored. In this study, Na4SiO4-based CO2 sorbents were prepared using four kinds of oxysalts as the dopants. The effects of acid radical ions/alkali metal cations, doping ratios and sorption/desorption temperatures on the CO2 capture performances of sorbents were investigated. The results showed that the promotion effects of CO32− and Li+/K+ ions were stronger than others, the maximum CO2 sorption capacity of Na4SiO4-30Li2CO3 and Na4SiO4-30K2CO3 at 700 °C reached 20.6 wt% and 19.5 wt%, respectively. The cyclic sorption capacity of Na4SiO4-30Li2CO3 was 8.5 wt%, which was 40.0% higher than that of Na4SiO4. Further, the oxysalt dopants could enhance the CO2 adsorption energy on the Na4SiO4 surfaces and reduce the energy level of the systems using density functional theory calculation, which were consistent with the experimental values. Finally, the effects of water vapor on the sorption of Na4SiO4 and Na4SiO4-K2CO3 were simulated, which could enhance the activity of O atoms on sorbent surfaces and promote rapid carbonization during the sorption progress. Thus, Na4SiO4 doped with oxysalts exhibit promising potential for high-temperature CO2 capture application.

Effect of water vapor on low temperature SCR performances over Cu and Mn-based catalysts: A comparison study

In this study, the commonly used Cu or Mn-based low-temperature SCR catalysts were employed to investigate their different reaction behaviors in the presence of high-content water vapor. Experimental results reveal that CuCeTi sample possesses superior water resistance at low temperature compared with MnCeTi catalyst. Upon the introduction of water vapor, both catalysts exhibit a quick loss in deNOx efficiency, while that is more pronounced on MnCeTi sample. In addition, unlike CuCeTi sample, MnCeTi catalyst also shows a gradual deactivation tendency after initial quick activity loss. Characterization and simulation results indicate that H2O is more easily adsorbed and dissociated on MnCeTi catalyst, showing stronger suppression on NH3 adsorption, causing more serious initial deactivation. Furthermore, more abundant hydroxyl groups derived from dissociative adsorption of water on MnCeTi catalyst will lead to more NH4NO3 deposition and the decrease in redox capacity. This is the main reason of gradual deactivation of MnCeTi catalyst at high-content water vapor. Such findings could pave a new way for development of highly efficient SCR catalysts with good water resistance for real application.

On the Chemical Effect of Steam Addition to Premixed Hydrogen Flames with Respect to NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {NO}_\ ext {x}$$\\end{document} Emissions and Flame Speed

The present work analyses the effect of water vapour addition on NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext {NO}_\ ext {x}}$$\\end{document} emissions of premixed hydrogen flames. In doing so, the adiabatic flame temperature is maintained by increasing the equivalence ratio, or alternatively increasing the unburned gas temperature, for increasing levels of water loading. Thus, it is possible to elucidate the changes in NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext {NO}_\ ext {x}}$$\\end{document} production at constant-temperature conditions when the mixture is diluted with water. A consistent reduction of NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext {NO}_\ ext {x}}$$\\end{document} emissions for increasing water dilution can be observed from 1-D premixed freely propagating flame simulations. Regarding the chemical kinetics effect of water vapour, the relative importance of different third-body reactions is examined by modifying the corresponding water collision efficiencies individually. For the chemical mechanism adopted, three reactions directly affect the nitrogen chemistry and the remaining relevant reactions are important for the flame structure and radicals concentration. The analysis stresses the importance of indirect effects like the formation and consumption of O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {O}$$\\end{document} and H\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {H}$$\\end{document} radicals in the pre-heat zone, which enhance the subsequent formation of NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext {NO}_\ ext {x}}$$\\end{document} within the flame. The presence of steam can lead to a reduction of approximately 50%\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$50\\%$$\\end{document} in NOx\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext {NO}_\ ext {x}}$$\\end{document} emissions under conditions close to stoichiometry and high water loading (10%\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$10\\%$$\\end{document} by mass), compared to scenarios without water addition. Furthermore, the efficiency of water in third-body reactions significantly contributes to an emission reduction, and half of NO\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {NO}$$\\end{document} emissions under the same water loading conditions at high equivalence ratio are observed when the third-body reaction efficiency is activated with respect to the case with zero efficiency. This reduction is primarily attributed to effects on radical concentrations. Finally, the chemical effect via the third-body efficiency of water is examined with respect to flame speed. It turns out that the adiabatic flame temperature plays a key role for the relative influence of the chemical kinetics effect of water dilution. A cross-over temperature is found, below which the chemical effect of water reduces the flame speed, whereas the flame speed is increased above it.

Zero-dimensional analysis of the effect of water vapor on reducing electrons in the plasma sheath

In this study, an air-water vapor ionization reaction model is developed within the quantum-kinetic (Q–K) model of the direct simulation Monte Carlo method to investigate the detailed mechanism of how water vapor reduces electrons. The zero-dimensional simulations of a typical non-equilibrium flow field downstream of a normal shock are designed, where the electron number density decreases by two orders of magnitude due to water vapor. We conclude that the introduction of water vapor reduces the mole fractions of oxygen atoms and nitrogen atoms through five pairs of reactions and enhances the reverse nitric oxide associative ionization reaction, leading to electron consumption. The phenomena and corresponding mechanisms under varying mole fractions of water vapor, air temperatures, and water vapor temperatures are investigated. Based on the mechanisms, we propose that the addition of hydrogen ions could improve the water's mitigation effect, which is then proven to be able to reduce the electron number density by another two orders of magnitude, not only at high air temperatures but also at lower air temperatures or lower mass injection rates.

Passive direct air capture using calcium oxide powder: The importance of water vapor

Calcium oxide (CaO; lime) looping is a proposed technology with the potential to capture gigatonnes of carbon dioxide (CO2) from the atmosphere to help mitigate climate change. The importance of water in carbonation reactions is widely understood as it is needed for mineral and CO2 dissolution and carbonate precipitation. However, the effects of water vapor on CaO carbonation pathways and rates have yet to be elucidated in a systematic manner. Here, we examine the impact of relative humidity (RH) on CO2 removal using CaO powder at 20% to 95% RH. Higher RH resulted in faster hydration rates, forming Ca(OH)2 (portlandite); however, passivation limited carbonation in all experiments, with the greatest carbonation occurring at 80% RH (65% CaCO3; calcite). Thus, CaO powder is highly prone to passivation when using RH to drive hydration and carbonation. In RH swing experiments, RH was changed at different times (hours or days) and by different amounts (e.g., 40–99%). Humidity swings can yield >85% CaCO3 when complete CaO hydration at a low RH (<40%) occurs before carbonation at a high RH (∼99%). Importantly, separating these two processes yields nearly complete carbonation. In this case, we achieved a CO2 removal rate of 1 t CO2 for every 1.95 t of Ca(OH)2 per day.

Effect of water and ionic liquid vapors on the structural properties of gold nanoclusters formed during inert-gas condensation process using molecular dynamics simulations

In this research, process of Au nanocluster formation has been investigated using the inert-gas condensation process in different environments with different concentrations of Ar gas, water vapor, and IL molecules. We have calculated the total energy, relative stability, surface energy, and radial distribution function (RDF) of the different produced clusters at different simulation times. Our results showed that the number of formed clusters increases, whereas their size decreases by increasing the water and IL concentrations in the environment. The water and IL molecules adsorb on the nanoclusters surfaces and hinder the coalescence of the smaller clusters to form bigger clusters. The percentage of the fcc and hcp atoms also decreases by increasing the water and IL concentrations. The produced clusters also become more non-spherical by increasing the IL and water vapor in the environment (with exception of the pure vapors).