Low Hydrogen Concentration Research Articles

Tailoring the performance of the multidimensional electrostatically formed nanowire gas sensor

Abstract Multi-gate field effect transistors (FETs) based on silicon-on-insulator (SOI) have been popular for several decades due to their improved electrostatic control of the channel current between the source and the drain. Chemical sensors based on such multi-gate FET platform can leverage this improved electrostatic control to detect gases at very low concentration with ultrahigh sensitivity. Electrostatically formed nanowire (EFN) is a multiple-gate FET device which has proven to be an excellent platform for detecting volatile organic compounds and gases. In case of such multi-gate FET sensors, it is imperative to rigorously understand the influence of each gate in controlling the sensing performances. Using palladium nanoparticles decorated EFN (Pd-EFN) as an example, the current work presents a detailed methodology for determining the operating parameters for maximal sensing performances of the Pd-EFN sensor towards hydrogen sensing. We observed that a single operating point does not yield best results with regard to sensor response, dynamic range, and power efficiency. By optimising the operating points (by varying the different gate biases), a sensor response of 107 % was reached even at low concentrations of hydrogen (500 ppm) which is significantly lower than the lower explosive limit of 4% and a tunable dynamic range over three decades (4-8000 ppm) was obtained. Also, the sensor response was not compromised at low driving voltages (100 mV) thus contributing to low power consumption of the sensor. Such a correlation between the working point of the transistor and the various sensor performance metrics (maximum sensor response, dynamic range etc ) has not been studied before to the best of our knowledge and this study can be extended to EFN for other gases and any other multi-gate FET sensors (not limited to Si based sensors).This study can pave the way for effective design of future multi-gate transistors for gas sensing.

Bleaching efficacy of in-office bleaching with violet light using low-concentration hydrogen peroxide nanoparticulate photocatalyst gel: A randomized controlled trial

ObjectiveThis randomized controlled trial aimed to evaluate the bleaching efficacy and tooth sensitivity (TS) of participants submitted to different application protocols of in-office bleaching with violet light using 6 % hydrogen peroxide (HP) nanoparticulate photocatalyst gel. Materials and methodsSixty-six participants were randomized and bleached using either a 6 % HP (Nano White, DMC), and/or violet light (Bright Max Whitening, MMOptics), according to the following protocols: 1) only violet light (VIOL); 2) only bleaching gel application (BG) and; 3) combined bleaching gel application + violet light (BG+VIOL). The bleaching efficacy was evaluated with the Vita Easyshade spectrophotometer, Vita Classical and Vita Bleachedguide scales. The risk and intensity of TS were recorded using a 0–10 visual analogue scale (VAS) and a 0–4 numerical scale (NRS). Color change and intensity of TS values were compared using one-way ANOVA and Tukey's test were used. The absolute risk of TS was compared using the Chi-square test (α = 0.05). ResultsA significant and higher degree of bleaching was observed in the BG and BG+VIOL groups compared to the VIOL group (p < 0.003). Despite no significant differences in the risk (p > 0.07) and intensity (p > 0.28) of TS among groups, a higher risk of TS was observed in the BG and BG+VIOL groups. ConclusionsUsing VIOL reduced the risk of TS but did not improve bleaching. However, BG+VIOL with low-concentration HP nanoparticulate photocatalyst gel achieved equal efficacy and was less likely to cause TS compared to BG.

Control of hydrogen concentrations by microbial sulfate reduction in two contrasting anoxic coastal sediments.

Molecular hydrogen is produced by the fermentation of organic matter and consumed by organisms including hydrogenotrophic methanogens and sulfate reducers in anoxic marine sediment. The thermodynamic feasibility of these metabolisms depends strongly on organic matter reactivity and hydrogen concentrations; low organic matter reactivity and high hydrogen concentrations can inhibit fermentation so when organic matter is poor, fermenters might form syntrophies with methanogens and/or sulfate reducers who alleviate thermodynamic stress by keeping hydrogen concentrations low and tightly controlled. However, it is unclear how these metabolisms effect porewater hydrogen concentrations in natural marine sediments of different organic matter reactivities. We measured aqueous concentrations of hydrogen, sulfate, methane, dissolved inorganic carbon, and sulfide with high-depth-resolution and 16S rRNA gene assays in sediment cores with low carbon reactivity in White Oak River (WOR) estuary, North Carolina, and those with high carbon reactivity in Cape Lookout Bight (CLB), North Carolina. We calculated the Gibbs energies of sulfate reduction and hydrogenotrophic methanogenesis. Hydrogen concentrations were significantly higher in the sulfate reduction zone at CLB than WOR (mean: 0.716 vs. 0.437 nM H2) with highly contrasting hydrogen profiles. At WOR, hydrogen was extremely low and invariant (range: 0.41-0.52 nM H2) in the upper 15 cm. Deeper than 15 cm, hydrogen became more variable (range: 0.312-2.56 nM H2) and increased until methane production began at ~30 cm. At CLB, hydrogen was highly variable in the upper 15 cm (range: 0.08-2.18 nM H2). Ratios of inorganic carbon production to sulfate consumption show AOM drives sulfate reduction in WOR while degradation of organics drive sulfate reduction in CLB. We conclude more reactive organic matter increases hydrogen concentrations and their variability in anoxic marine sediments. In our AOM-dominated site, WOR, sulfate reducers have tight control on hydrogen via consortia with fermenters which leads to the lower observed variance due to interspecies hydrogen transfer. After sulfate depletion, hydrogen accumulates and becomes variable, supporting methanogenesis. This suggests that CLB's more reactive organic matter allows fermentation to occur without tight metabolic coupling of fermenters to sulfate reducers, resulting in high and variable porewater hydrogen concentrations that prevent AOM from occurring through reverse hydrogenotrophic methanogenesis.

A Highly Efficient Catalytic Co-Combustion of Aromatic and Oxygenated Volatile Organic Compounds (VOCs) via H2-Driven Onsite Heating

Catalytic combustion, a highly efficient technique for reducing volatile organic compounds (VOCs), is the focus of this study. We investigate the improved catalytic efficiency of the physical mixing of nanosized Pt and atomically dispersed Co, supported on Al2O3 catalysts (Pt-Co)/Al2O3 (PM) for the catalytic combustion of VOCs. The catalyst efficiency is evaluated for the hydrogen-assisted catalytic oxidation of various VOCs, including aromatic and oxygenated VOCs such as benzene, toluene, methanol, and formic acid. Our study aims to understand the impact of hydrogen incorporation on the combustion process of various VOCs. The findings of this work underscore the potential of hydrogen-assisted catalytic ignition, which can achieve ignition at ambient temperature, a significant departure from conventional electric heating that typically requires additional energy to raise the temperature. Various characterization techniques, such as BET, STEM, and XRD, are employed to assess the structure–activity relationship of the catalyst. The optimal hydrogen concentration for complete VOC conversion is 3%. Notably, even at a lower hydrogen concentration of 2%, benzene and methanol reach an ideal ignition temperature of over 500 °C when introduced into the physically mixed catalyst. This study highlights the significant potential of hydrogen-assisted catalytic combustion, inspiring further research and offering a promising method to reduce VOCs effectively.

Tri-functional carbon membrane for one-step uptake of low-concentration hydrogen to high purity

The uptake of hydrogen (H2) from natural gas pipelines (CH4) through membrane separation technology is an efficient avenue of obtaining H2 resources. Carbon membranes have the potential to be an attractive option for energy-efficient gas separations in the next generation of membranes due to their precise molecular discrimination ability and easy scalability. Here, we report a carbon membrane composed of a mesoporous substrate, seed layer and sieving layer, achieving a one-step uptake with 55.3 × 10-9 mol·m−2·s−1 Pa−1 permeance and a separation factor for H2/CH4 of 359.1 by feeding hydrogen (20 vol%). As revealed by the kinetic diffusion experiment, H2 is transported in mesoporous substrate via Knudsen flow, differing from the transition flow taken by CH4, thus H2 diffusion rates exceed CH4 by an order of magnitude, which substantially increased H2 purity from 20 vol% to higher purity as gas mixtures passed through the substrate. Then, the H2 passed through the seed layer and sieving layer, resulting in a final H2 purity of ∼ 99 vol%, a sharp increase from the initial low concentration. This carbon membrane integrates three functions of capture, pre-separation and purification into one material and provides a new solution for the uptake of H2 from CH4.

Quantitative estimation method of the effect of segregated solute on hydrogen-enhanced decohesion at a grain boundary

Hydrogen-enhanced decohesion (HEDE) is a proposed mechanism of hydrogen-induced grain boundary (GB) fracture in metals and has been widely calculated from first principles over the past decade. However, the effect of GB-segregated solutes on HEDE is complex and rarely quantified. This study presents a quantitative numerical estimation method based on statistical thermodynamics using first-principles calculations of multiple hydrogen trappings at a GB and its fracture surfaces with segregated solutes. This method accurately estimates the lattice-dissolution-hydrogen-dependent HEDE, including the interactions caused by the segregated solute: the decohering or cohesion-enhancing effect of the solute itself, solute-hydrogen interaction, solute-affected hydrogen-hydrogen interaction, and mobile hydrogen effect. We present a trial calculation to examine how the attractive interaction between solute and hydrogen influences HEDE, showing that HEDE can be induced at lower hydrogen concentrations if not canceled by other interactions.

A Model to Account for the Effects of Load Ratio and Hydrogen Pressure on the Fatigue Crack Growth Behavior of Pressure Vessel Steels.

A phenomenological model for estimating the effects of load ratio R and hydrogen pressure PH2 on the hydrogen-assisted fatigue crack growth rate (HA-FCGR) behavior in the transient and steady-state regimes of pressure vessel steels is described. The "transient regime" is identified with crack growth within a severely embrittled zone of intense plasticity at the crack tip. The "steady-state" behavior is associated with the crack growing into a region of comparatively lower hydrogen concentration located further away from the crack tip. The model treats the effects of R and PH2 as being functionally separable. In the transient regime, the effects of the hydrogen pressure on the HA-FCGR behavior were negligible but were significant in the steady-state regime. The hydrogen concentration in the steady-state region is modeled as being dependent on the kinetics of lattice diffusion, which is sensitive to pressure. Experimental HA-FCGR data from the literature were used to validate the model. The new model was shown to be valid over a wide range of conditions that ranged between -1≤R≤0.8 and 0.02≤PH2≤103 MPa for pressure vessel steels.

Effect of a novel low-concentration hydrogen peroxide bleaching gel containing nano-sized sodium trimetaphosphate and fluoride

ObjectivesTo evaluate in vitro the effects of nano-sized sodium trimetaphosphate (TMPnano) and sodium fluoride (F) added to a 17.5 % hydrogen peroxide (H2O2) bleaching gel on the color change, enamel mechanical and morphological properties, and H2O2 transamelodentinal diffusion. Materials and MethodsBovine enamel/dentin discs (n = 180) were divided according to the bleaching gel: 17.5 % H2O2 (17.5 % HP); 17.5 % H2O2 + 0.1 % F (HP/F); 17.5 % H2O2 + 1 % TMPnano (HP/TMPnano); 17.5 % H2O2 + 0.1 % F + 1 % TMPnano (HP/F/TMPnano) and 35 % H2O2 (35 % HP). The gels were applied for 40 min on three sessions, each session spaced 7 days apart. The total color change (ΔE*ab) according to the Commission Internationale de l'Eclairage (CIE) L*a*b* color change measured by CIEDE2000 (ΔE00), whitening index (ΔWID), surface hardness (SH), surface roughness (Ra), cross-sectional hardness (ΔKHN), and transamelodentinal diffusion were assessed. Enamel surfaces were examined using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDS) analysis. The data were analyzed using ANOVA, followed by the Student-Newman-Keuls test (p < 0.05). ResultsΔE*ab, ΔE00, and ΔWID values were comparable among the gels that produced a bleaching effect post-treatment (p < 0.001). The HP/F/TMPnano group exhibited lower mineral loss (SH and ΔKHN), Ra, and H2O2 diffusion compared to the 17.5 % HP and 35 % HP groups, which had the highest values (p < 0.001). SEM/EDS analysis revealed surface changes in all bleached groups, though these changes were less pronounced with F/TMPnano. ConclusionsThe 17.5 % HP gel containing F/TMPnano maintains the bleaching effect while reducing enamel demineralization, roughness, H2O2 diffusion, and enamel morphological changes. Clinical RelevanceLow-Concentration H2O2 bleaching gel containing F/TMPnano can be used as a novel approach to enhance safety and maintain the performance of aesthetic effects.

Hydrogen embrittlement of Zircaloy-4 fabricated by ultrasonic additive manufacturing

Ultrasonic additive manufacturing (UAM) was successfully applied to the zirconium material system to create a planar geometry. Following fabrication, SS-J3 type tensile specimens of the UAM and wrought Zircaloy-4 with a nominal gage section of 5 × 1.2 × 0.75 mm were machined for hydriding studies and mechanical testing. The SS-J3 type tensile specimens were gas-charged with hydrogen using a custom system that precisely controls hydrogen gas flow rate, hydrogen partial pressure, and temperature. To avoid altering the UAM material, the maximum process temperature was limited to 550 °C. Using different initial hydrogen gas pressures and flow rates, various hydrogen contents (70–1755 wppm) were achieved for Zircaloy-4 specimens. Tensile testing shows that, regardless of hydrogen content, all UAM specimens measured yield strengths in the range of 557 ± 16 MPa and ultimate tensile strengths of 660 ± 4 MPa. However, total elongation clearly decreased as a function of increasing hydrogen content. At the lowest hydrogen content, the total plastic elongation measured 21.5 %, and this value decreased to less than 2 % when the hydrogen content was increased to 1000 wppm. Cross-sectional optical microscopy images revealed that the hydride distributions are randomly oriented. For the low hydrogen content specimen, these randomly distributed hydrides are isolated from each other. A sandwiched structure, consisting of high-density and low-density layers, was also observed for the specimens with hydrogen content between 200 and 400 wppm. As the hydrogen content increases, the hydrides diffuse into the low-density hydride layers to form a network across the whole specimen. Although the tensile properties of UAM and wrought Zircaloy-4 exhibit the same behavior with increasing hydrogen content, the distinctions in grain orientations led to differences in the hydride orientations at low and intermediate hydrogen concentrations.

Automated Standardization of Melanin Bleaching Procedures of Heavily Pigmented Melanocytic Lesions With Low-Concentration Hydrogen Peroxide on an Automated Platform.

Melanin is a natural pigment in the human body that is primarily found in the skin and hair. It protects the skin from damage by ultraviolet radiation. Although this pigment plays a crucial role in protecting the human body, it represents a challenge for pathologists to evaluate highly pigmented tissue samples from melanoma or pigmented skin lesions. Abundant melanin may obscure tissue morphology, which makes it very difficult for pathologists to make a differential diagnosis. Melanin pigment is brown-to-black and granular, and its distribution is often uneven in tissues. The presence of these pigments can complicate the analysis of immunohistochemistry (IHC) for 2 reasons. First, they have a direct physical masking effect on antigen-antibody interactions. Second, 3,3-diaminobenzidine, the most commonly used chromogen, has a brown color that is difficult to distinguish from melanin pigment. Therefore, melanin bleaching has become a crucial step in handling pigmented melanocytic lesions. Bleaching techniques aid pathologists in histopathologic examination of melanin-rich tissue. In this study, we integrated melanin bleaching and IHC on an automated IHC platform to set up a rapid and fully automated procedure. Bleaching steps were performed before antigen retrieval. Samples were treated with 1% hydrogen peroxide solution in Tris-HCl buffer (pH 10) at 80°C for 8 minutes, achieving optimal conditions for melanin bleaching while preserving tissue morphology and antigenicity. This rapid, effective, fully automated, and standardized workflow can be applied to routine staining procedures in clinical laboratories, thereby improving the quality of pathological diagnosis.

High sensitivity gas detection based on Au waveguide

Hydrogen, as a representative of the new energy source, has great potential for development, and the detection of the low concentration of hydrogen plays a crucial role in process safety control. In this paper, a gas sensor based on a metal-insulator-metal (MIM) structure with high sensitivity and low response time is proposed. The sensor is bilaterally coupled with a ring resonant cavity and a metal nanopillar, and the outgoing field superposition is achieved by bilaterally coupling the resonant cavity to achieve a lower transmittance, which facilitates detection. The symmetry of the structure was broken by different methods, and the results showed that the complexity and response time of the structure increased significantly after breaking the symmetry, but the transmittance appeared to decrease and the transmission characteristic curve was independent of the coupling phase. The waveguide structure shows a highly linear relationship between resonance wavelength and refractive index with a maximum sensitivity of 2433.00 nm/RIU when used for refractive index sensing, and a maximum sensitivity of −2.61 nm/% when used for hydrogen gas sensing. For methane gas sensing, the maximum sensitivity is −9.22 nm/%.

Achieving ultralow contact resistance and reducing residual hydrogen by surface doping

Indium gallium zinc oxide (IGZO)-based materials and devices hold a significant position in integrated circuit manufacturing industries, yet challenges persist in controlling residual hydrogen and managing high source/drain contact resistance. Our proposed hypothesis not only targets the control of residual hydrogen through out-diffusion but also offers an opportunity for surface doping of IGZO, promising a substantial reduction in contact resistance. Interestingly, a 30 s hydrogen plasma deposition resulted in a lower hydrogen concentration compared to the residual hydrogen in IGZO, leading to increased carrier density at the interface. The higher carrier density, coupled with metallization-induced band bending at the interface, significantly lowers the Schottky barrier height and density of states, thereby facilitating sophisticated electron transport between molybdenum and IGZO. To the best of our knowledge, this study represents the first substantial reduction in residual hydrogen from IGZO films (initially deposited at 1020 cm−3, reduced to 1019 cm−3), while achieving ultralow specific contact resistivity (2.47 × 10-9 Ω•cm2) and sheet resistance (177.67 Ω/□). Our hypothesis introduces a novel strategy to reduce contact resistance in electronic devices.

Hydrogen extraction from 0.1 % H2–He mixture: The interplay phenomena of electrode, temperature, and voltage in BZYN & BZCYYb

Hydrogen pumps, crafted from proton-conductive ceramic electrolyte and paired with either oxide or metallic electrodes, have been designed for the extraction of hydrogen isotopes from helium gas mixtures containing 0.1 % hydrogen isotopes, particularly within the context of TES for nuclear fusion reactors. This study presents the electrochemical hydrogen permeation research conducted on the perovskite proton conductor materials BaZr0.1Ce0.7Y0.1Yb0.1O3-δ (BZCYYb) and BaZr0.8Y0.16Ni0.04O3-δ (BZYN) under these operational conditions. It was observed that nickel electrodes provided superior performance over SrFe0.8Mo0.2O3-δ (SFM) electrodes in terms of hydrogen extraction efficiency. Hydrogen pumps that integrated BZCYYb as the electrolyte with nickel electrodes showed enhanced efficiency, while those utilizing BZYN as the electrolyte coupled with nickel electrodes demonstrated greater stability. Furthermore, the study explored the voltammetric nonlinearity at low hydrogen concentrations and the dependency of concentration polarization efficiency on both voltage and temperature, aiming to establish optimal conditions that balance stability and efficiency for both types of hydrogen pumps.

The influence of solid solution hydrogen and precipitated hydride on the creep behavior of Zircaloy-4

The effect of hydrogen on the creep rates of Zircaloy-4 claddings especially in the low hydrogen concentration remains largely unexplored while creep is considered a main mechanism for spent nuclear fuel failure along with hydride-induced mechanisms. Here, we study the influence of hydrogen on the creep behavior of low burnup Zircaloy-4 cladding from a microstructural perspective. The creep tests at 450 °C and 120 MPa reveal that specimens with hydrogen contents below the terminal solid solubility for dissolution (TSSD) at the test temperature exhibited decreased creep resistance as hydrogen concentration increased, while those with hydrogen contents above the TSSD demonstrated increased creep resistance with higher hydrogen concentration. The lowest creep resistance occurs at the hydrogen concentration corresponding to the TSSD. Additional microstructural analyses using electron backscattered diffraction (EBSD) show the increasing intra-granular/inter-granular hydride ratio in the post-crept specimens as the hydrogen concentration decreases, suggesting that hydrogen atoms in solid solution aid creep progression. Also, an increased amount of twin boundaries is observed in post-crept specimens with hydrogen concentration above TSSD. These results suggest that creep assessment in spent nuclear fuels may require caution especially in low-burnup regime.

Efficient formation of propylene oxide under low hydrogen concentration in propylene epoxidation over Au nanoparticles supported on V-doped TS-1

The direct epoxidation of propylene to propylene oxide (PO) represents a unique feature of gold nanoparticle catalysts. Different amounts of vanadium were introduced into TS-1 using a hydrothermal method to give V-TS-1, and the effect of various vanadium loadings on the catalytic performance of Au/V-TS-1 was investigated in the epoxidation of propylene under different reaction conditions. The obtained characterization results indicate that the molecular sieve pore structure and crystalline phase structure of TS-1 were maintained after vanadium incorporation, and vanadium was incorporated into the molecular sieve framework. The introduction of an appropriate amount of vanadium resulted in the homogeneous dispersion of gold particles with a small average particle size, which facilitated the epoxidation reaction. When V was introduced into TS-1, the propylene conversion decreased under the condition of 10 % H2 concentration (C3H6/H2 = 1/1) in the reaction atmosphere, but the PO selectivity was maintained. Interestingly, when the H2 concentration in the reaction atmosphere was lowered to 2 % (C3H6/H2 = 3/1), the propylene conversion in Au/TS-1 was significantly decreased compared to 10 % H2 concentration condition, while in Au/V-TS-1, the propylene conversion was maintained in 2 % H2 concentration condition compared to 10 % H2. Au/V-TS-1 also maintained its selectivity for PO even when the H2 concentration was lowered. Therefore, under low hydrogen concentration conditions, the PO formation rate of Au/V-TS-1 was much higher than that of Au/TS-1. More, the same trend was observed when Mo was added in place of V. Our strategy will guide the design of future catalysts as a way to utilize hydrogen more effectively while maintaining PO productivity.

Non-Henrian behavior of hydrogen in plagioclase – basaltic melt partitioning

Plagioclase crystals in lunar anorthosite may have formed directly from the lunar magma ocean (LMO), with their elemental and isotopic compositions providing unique probes of LMO composition, age, and evolution. Low hydrogen concentrations have been reported in lunar plagioclase, but translating this to estimates of LMO hydrogen contents is complicated by incomplete knowledge of hydrogen partitioning between plagioclase and melt at low hydrogen contents. We conducted a series of high-temperature experiments to better quantify the plagioclase-melt partition coefficient of hydrogen in the Moon at low melt H abundances. Hydrogen contents of plagioclase and coexisting melt, reported in terms of water equivalent concentrations, were analyzed using Fourier Transform Infrared Spectroscopy. Resulting plagioclase-melt partition coefficients of water, Dplag-melt water, at melt water contents below 300 ppm, are 0.10 ± 0.05 to 0.36 ± 0.19. the highest Dplag-melt water reported to date. Our results, in conjunction with literature data, indicate a strong dependence of Dplag-melt water on water concentration in the melt (x in ppm): Dplag-melt water=20±5·x−0.88±0.03. This strong non-Henrian behavior is likely related to changes in the hydrogen activity in basaltic melt due to variations in H2O/OH speciation as a function of melt hydrogen content, implying that hydrogen partitioning in other mineral-melt systems may also be non-Henrian. At the low water contents in the lunar interior, Dplag-melt water is approximately 2 orders of magnitude higher than previously assumed. If hydrogen contents measured in lunar plagioclase crystals reflect pristine plagioclase-LMO equilibrium without subsequent modification, we conclude that <14 ppm H2O equivalent would have been present in the Moon when 95% of the initial LMO had crystallized.

Experimental investigation of the characteristics of combustion in the full hydrogen blending range of methane-hydrogen mixtures in a MILD model combustor

MILD combustion technology is expected to enable safe and stable low-emission combustion of hydrogen-doped fuels, or pure hydrogen fuels, in gas turbines designed for zero-carbon emissions. To improve combustion stability at high hydrogen content while maintaining low NOx emissions, a MILD model combustor was modified, specifically the upstream fuel/air distribution and mixing method. And the combustion stability of the modified MILD combustor was significantly extended. Here, the combustion characteristics of the modified MILD combustor are experimentally investigated at 0–100% hydrogen contents. The investigation results demonstrate that unlike the combustion stability region at low hydrogen concentrations, a narrow thermoacoustic instability region occurs at 60% hydrogen content. As the hydrogen content increases, the instability region becomes narrower while shifting towards lower equivalence ratios. The change in hydrogen content is accompanied by a significant peak energy migration of the dynamic pressure. The OH* chemiluminescence images showed that the heat release zone became more concentrated with increasing hydrogen content. And the dominance of high-frequency peak energy correlates to lateral motion, whereas the dominance of low-frequency peak energy corresponds to axial motion. This transition in flame dynamics occurs not only for different hydrogen contents but also for different equivalence ratios of pure hydrogen combustion. In contrast, NOx emissions are not sensitive to hydrogen content. At the same time, the MILD model combustor produces low emissions, with NOx emissions of less than 10 ppm@15%O2 at adiabatic flame temperatures ranging from 1200 K to 2100 K. These results show that the MILD model combustor has favorable fuel suitability.

Low detection based on Pd Pt /In2O3 nanospheres for rapid hydrogen detection

Semiconductor gas sensors still have limitations in realizing rapid hydrogen measurement in lower hydrogen concentration environments. Therefore, in this paper, In2O3 cloud-like spherical hydrogen detection sensing materials with different Pd and Pt ratio loading were successfully prepared using the water bath method. The In2O3 sensing materials modified with noble metals Pd and Pt were designed for the rapid detection of hydrogen at 400 ppb with good selectivity under mixed gas components. The crystalline phase, morphology, and chemical composition of the prepared Pd and Pt-loaded In2O3 samples were analyzed using characterization techniques. The gas-sensing results showed that the In2O3 gas-sensing sensor with a Pd and Pt ratio loading of 1–2 had stronger H2 sensing performance at the optimum operating temperature (350°C). The response time and recovery time of In2O3 loaded with the opinion ratio at 350℃ and 400 ppb were 1 s and 15 s. The low detection limit was 400 ppb, with good repeatability and long-term stability. Finally, the enhanced gas sensitization mechanism of the In2O3 gas sensor loaded with Pd and Pt for H2 was discussed.

Ferrate(VI)/percarbonate for the oxidation of micropollutants: Interactive activation and release of low-concentration hydrogen peroxide for efficient electron utilization

A novel "ferrate/percarbonate (Fe(VI)/SPC) co-oxidation process" was used to treat ciprofloxacin (CIP) and various micropollutants (MPs), which owned better performance than mixture of Fe(VI), Na2CO3 and H2O2. The mechanism investigation found that the low-concentration H2O2 (1–2 µM) released by SPC can promote the high-valent iron intermediates (Fe(IV)/Fe(V)) of Fe(VI) to the MP oxidation, and Fe(VI) products can also activate SPC to produce hydroxyl radical (·OH). The interactive activation of Fe(VI) and SPC was realized, which retained the high selectivity of Fe(VI) to electron-rich pollutants, and also made up the oxidation of electron-deficient pollutants through •OH, improving the degradation effect of various MPs by 20–30%, and the rate constant was increased by 1 to 3 times. Moreover, non-purgeable organic carbon (NPOC) determination confirmed that •OH participation reduced the NPOC value of CIP from 5.43 mg/L to 4.37 mg/L. The transformation pathway of CIP showed that Fe(VI)/SPC resulted in more hydroxylation intermediates of CIP than Fe(VI) alone. Acute toxicity assays found that the photoinhibition rate of CIP treated with Fe(VI) alone was 14.5%, while the sample treated with Fe(VI)/SPC showed no significant photoinhibition effect, which proved that the new process had good detoxification properties for CIP.

Hydrogen enhanced localised plasticity of single grain α titanium verified by in-situ hydrogen microcantilever bending

The effect of hydrogen on the micromechanical characteristics of pure grade 2 titanium was investigated by comparing prenotched microcantilever bending in air versus in-situ electrochemical hydrogen charging. The nanoscale interaction between hydrogen and the metal's defects was analysed in three different grain orientations, i.e. the top surface parallel to {101‾2}, {0001}, and {202‾1}. The subsequent high resolution post-mortem characterisation enabled to characterise the interplay between hydrogen in solid solution and the dislocations in the local deformation process. The results showed that hydrogen facilitated a localised plasticity mechanism, causing hydrogen assisted degradation at the applied low hydrogen concentration below the hydride formation threshold. Meanwhile, hydrogen provoked a reduction in defect formation energy, following the defactant concept, which was responsible for a softening effect on the yield stress and flow stress. Furthermore, due to the anisotropic characteristics of the α titanium hexagonal close packed crystal lattice, the susceptibility to hydrogen effects also depended on the grain orientation. This single grain in-situ micromechanical testing is complementing the existing macroscaled identification of hydrogen effects in α titanium.