Hydrogen Content Research Articles

Nagynyomású hidrogénatmoszférás kemence gyártása szénacélok elridegedésének vizsgálatához

Összefoglalás. A hidrogén tárolása iránti igény egyre növekszik, melynek oka az, hogy a hidrogén mint alternatív energiahordozó jelentős szerepet játszik a szén-dioxidkibocsátás-csökkentési törekvésekben. Azonban, az elridegedési folyamatok körében a hidrogén által előidézett károsodások jelentik a legkomolyabb problémát az acélokra nézve. Kutatómunkánk során egy nagynyomású hidrogénatmoszférás hőkezelésre alkalmas autoklávot terveztünk, majd gyártottunk. Az autoklávban P355 NH minőségű alapanyagból kimunkált szabványos Charpy-féle ütőpróbatesteket hőkezeltünk 150 °C-on, 40 bar túlnyomáson, 200 órán keresztül, tiszta hidrogén atmoszférában. A vizsgálatok eredményei alapján megállapítottuk, hogy a jelentős mértékű elridegedés a hidrogénezési folyamat után sem történt. Summary. The demand for hydrogen storage is growing. The primary reason for this is that hydrogen as an alternative energy carrier is playing a significant role in carbon reduction efforts as a fuel for road and maritime transport. In addition, hydrogen can be seen as a long-term flexible energy storage option. Hydrogen as an energy carrier is expected to play a significant role in residential and industrial use in the future. A first step in this development is the mixing of hydrogen with natural gas in small quantities. Increasing the share of hydrogen would not only reduce CO2 emissions, but would also facilitate the development of different hydrogen production methods and thus reduce production costs. The upper safety limit for hydrogen blending with natural gas is set by the national specification of the natural gas supply, possible material quality restrictions and the tolerance of the most sensitive equipment in the network. For this reason, the maximum allowable hydrogen content in natural gas is generally limited to 2,5%. However, among the embrittlement processes, hydrogen-induced damage is the most serious problem for both non-alloy and low-alloy steels. Atomic hydrogen diffuses in steel at high rates. The diffusion rate is orders of magnitude higher than that of other elements; this is due to the small atomic diameter of hydrogen. To investigate the degradation of different carbon steels in a high-pressure hydrogen atmosphere, a hydrogenation furnace was designed and fabricated at the Department of Materials Science and Engineering at BME. The hydrogenation furnace is the main part of a complex mechanical engineering system, for the operation of which the mechanical, heating, electrical supply, control and gas handling components are indispensable. The entire design process of the furnace was led by József Blücher, Professor Emeritus at BME, with the help of the engineers and technicians working on the project. Standard Charpy impact test specimens were machined from P355 NH grade material to test the embrittlement of carbon steels. The hydrogenation temperature was 150 °C, the internal overpressure in the chamber was 40 bar, the hydrogenation time was 200 hours and the atmosphere was hydrogen gas of purity 5.0. The impact test was carried out at -20, 0 and +20 °C. Based on the results of the tests, it can be concluded that there was no significant degree of degradation both before hydrogenation and after prolonged exposure to hydrogen. It can be concluded that the tube material used as a sample is suitable for operation in a hydrogen medium. Based on the analysis of the burst areas and impact values of the impact test specimens, it was concluded that hydrogen did not cause any observable damage to the test material.

Production and New Green Activation of Conductive 3D-Printed Cu/PLA Electrode: Its Performance in Hydrogen Evolution Reactions in Alkaline Media

In this study, Cu-polylactic acid (PLA) composite filaments were produced with an extruder and three-dimensional (3D) Cu/PLA electrodes were 3D printed with Fused Deposition Modelling (FDM) method. To improve the electrochemical performance of the 3D-Cu/PLA electrode, a novel electrochemical activation method, which differentiates from complex activation methods in the literature, was applied in 1 M KOH solution without using any solvent. Field emission scanning electron microscopy (FE-SEM), Energy-Dispersive X-ray Spectroscopy (EDX), Fourier Transform Infrared Spectroscopy (FT-IR), and RAMAN techniques were used to characterize the 3D-Cu/PLA electrode before and after activation. The results showed that Cu particles were released after the degradation of PLA after activation. In addition, the thermal stability of the 3D electrode was demonstrated by the TGA technique. The performance of the 3D Cu/PLA electrode before and after activation in the hydrogen evolution reaction (HER) in 1M solution was measured using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and cathodic polarization curves methods. The EIS results showed that the charge transfers resistance values of the 3D-Cu/PLA electrode in 1 M KOH decreased significantly after activation. Post-activation hydrogen content measurements of the 3D-Cu/PLA electrode after electrolysis at different potentials and energy efficiency tests at different current densities were also carried out. The results indicate that the electrocatalytic properties of 3D-Cu electrodes were improved for HER through the activation process.

Hydrothermal liquefaction of composite household waste to biocrude: the effect of liquefaction solvents on product yield and quality.

The hydrothermal liquefaction (HTL) of composite household waste (CHW) was investigated at different temperatures in the range of 240-360 °C, residence times in the range of 30-90 min, and co-solvent ratios of 2-8 ml/g, by utilising ethanol, glycerol, and produced aqueous phase as liquefaction solvents. Maximum biocrude yield of 46.19% was obtained at 340 °C and 75 min, with aqueous phase recirculation ratio (RR) of 5 ml/g. The chemical solvents such as glycerol and ethanol yielded a biocrude percentage of 45.18% and 42.16% at a ratio of 6 ml/g and 8 ml/g, respectively, for 340 °C and 75 min. The usage of co-solvents as hydrothermal medium increased the biocrude yield by 35.30% and decreased the formation of solid residue and gaseous products by 19.82% and 18.74% respectively. Also, the solid residue and biocrude obtained from co-solvent HTL possessed higher carbon and hydrogen content, thus having a H/C ratio and HHV that is 1.01 and 1.23 times higher than that of water as hydrothermal medium. Among the co-solvents, HTL with aqueous phase recirculation resulted in higher carbon and energy recovery percentages of 9.36% and 9.78% for solid residue and 52.09% and 56.75% for biocrude respectively. Further qualitatively, co-solvent HTL in the presence of obtained aqueous phase yielded 33.43% higher fraction of hydrocarbons than the pure water HTL and 7.70-17.01% higher hydrocarbons when compared with ethanol and glycerol HTL respectively. Nitrogen containing compounds, such as phenols and furfurals, for biocrudes obtained from all HTL processes, were found to be present in the range of 8.30-14.40%.

Modeling hydrogen diffusion in precipitation hardened nickel-based alloy 718 by microstructural modeling

Abstract Environmentally assisted cracking can significantly affect the performance of high strength alloys and limit material selection to minimize the risk of subcritical crack growth in service. UNS N07718 is widely used in marine service applications and under a variety of conditions, such as: alternate immersion, different levels of cathodic protection, and freely corroding galvanic couples, because of its demonstrated corrosion and fracture resistance in these environments. In this work we developed a representative model of the material microstructure including the metal grains, the material texture, and the precipitates along the grain boundaries and within the grains. The microstructural model was subjected to the boundary conditions identified at the notch root of a fracture mechanics sample and the results are used as input for a simulation of hydrogen diffusion from the surface of the notch, assuming the material has been introduced to a hydrogen producing environment. The diffusion of hydrogen was modeled by Fick’s law and included both hydrostatic stress and mobile dislocation velocity as driving forces. The influence of immobile dislocations was also modeled to account for the irreversible trapping. The results show that hydrostatic stress and immobile dislocation trapping can significantly alter the highest concentration of hydrogen and its location within the microstructure towards the fracture process zone. Mobile dislocation velocity has a small influence in determining the hydrogen distribution near the fracture process zone.

Importance of pyrolysis temperature and particle size on physicochemical and adsorptive properties of urban wood-derived biochar

Physicochemical properties of biochars made from urban wood waste at different pyrolysis temperatures (400-700 °C) and particle sizes (1-2 mm and 63-75 μm) were compared to their ability for heavy metals adsorption at various contact times (30-300 min) and adsorbent dosages (0.1-5 g L-1) in real landfill leachate. The yield, volatile matter, hydrogen and oxygen contents, and functional groups of biochars decreased with increasing pyrolysis temperature; while pH, electrical conductivity, ash, fixed carbon, and specific surface area (SSA) increased. FE-SEM images showed that the creation of pores on the surface of biochars increased significantly with increasing pyrolysis temperature. Moreover, particle size exhibited no significant effect on the properties of biochars (p>0.05), except for the SSA. The SSA of biochars with a particle size of 63-75 μm was significantly higher than that measured in 1-2 mm biochars. The adsorption efficiency of heavy metals from landfill leachate increases with increasing pyrolysis temperature, contact time and adsorbent dosage. Conversely, reducing the particle size increases the adsorption efficiency. The highest adsorption efficiency for Pb, Zn, Ni, Cd, and Mn was obtained as a result of using biochar pyrolyzed at 700 °C with a particle size of 63-75 μm (i.e., BC700/63-75) by 60.39%, 75.01, 64.36, 58.87%, and 71.15%, respectively. Pseudo second-order kinetic and the Langmuir isotherm were recognized as the most appropriate models to describe the adsorption process. The chemical adsorption was identified as the main mechanism for the adsorption of metal ions onto BC700/63-75.

Effects of Hydrogen Bonding in Silicon Nitride/Polyimide Passivation Bilayer in SiC Power Devices

Composition and morphology of two types of bilayers of plasma‐enhanced chemical vapor deposition hydrogened silicon nitride (SiNx:H) and polyimide (PI), as effcient barrier against moisture in SiC‐based power devices, are investigated. Two types of silicon nitrides are obtained by changing the flow ratios of the SiH4 and NH3 precursors. Rutherford Backscatterered analyses show that the Si/N ratio varies from 0.6 to 0.8. Elastic recoil detection analyses show that the sample with higher nitrogen content has a higher total bound hydrogen content of 7.8 × 1017 cm−2 with respect to the 7.1 × 1017 cm−2. Fourier‐transform infrared spectroscopy characterizations show Si–H group concentrations of 0.96 × 1017 and 6.86 × 1017 cm−2 and NH groups of 4.82 × 1017 and 2.28 × 1017 cm−2, respectively. Silicon nitride films with higher concentration of N–H groups show higher reactivity and permeability to water, making them less effective as a barrier layer. Atomic force microscopy analyses of a PI layer deposited on the nitride layer, SiNx:H/PI show for both type of samples a similar roughness, indicating planarization that can increase the adhesion of SiNx:H/PI and resistance to moisture. The delamination mechanism of the bilayer under pressure pot test conditions is proposed.

The Effects of Different Concentrations of Hydrogen-Rich Water on the Growth Performance, Digestive Ability, Antioxidant Capacity, Glucose Metabolism Pathway, mTOR Signaling Pathway, and Gut Microbiota of Largemouth Bass (Micropterus salmoides)

Hydrogen-rich water (HRW) is widely recognized for its growth promoting, antioxidant, and anti-inflammatory properties. However, little is known about the role of HRW in aquaculture. This study aims to investigate how different concentrations of HRW affect the growth performance, digestive ability, antioxidant capacity, mTOR signaling pathway, and gut microbiota of juvenile largemouth bass. We randomly assigned 360 fish (13.73 ± 0.1 g) to three treatments. The control group was maintained in regular water, while the treatment groups were treated with different concentrations of H2 dissolved in water, which were H1 (179.65 ± 31.95 ppb) and H2 (280.65 ± 64.43 ppb), respectively. Through an analysis of the three treatments, it was found that H1 significantly increased the final body weight, weight gain rate, specific growth rate, and survival rate, and reduced the feed conversion ratio (p < 0.05). In addition, the trypsin activity was significantly increased in the intestine (p < 0.05), and the expression of genes related to the glucose metabolism (pk and pepck) and mTOR (tor, akt, s6k1, 4ebp1, and ampka) signaling pathways were significantly increased in the liver in H1 (p < 0.05). The relative abundance of Blautia in the gut microbiota (p < 0.05) was significantly increased in H1. Therefore, these results indicated that H1 can significantly improve growth performance, promote intestinal digestion, activate the glucose metabolism pathway and mTOR signaling pathway, and increase the abundance of beneficial bacteria in the gut of largemouth bass. These findings provided valuable support for the application of HRW to support the healthy aquaculture of largemouth bass.

Exploring the application of hydrazine hydrate in protonic ceramic fuel cells: Strategies and performance improvements

Hydrazine hydrate, characterized by its high hydrogen content and eco-friendliness, garners extensive attention in the field of fuels. Its high energy density and rapid decomposition capabilities render it a promising fuel option for Proton-Conductor Solid Oxide Fuel Cells (PCFCs). Given the unique properties of hydrazine hydrate, this study employs a dendritic porous anode structure to facilitate faster fuel transport. Additionally, the influence of operational temperature and concentration of hydrazine hydrate as fuel on cell performance is analyzed. An effective vapor management strategy is implemented to address its decomposition into water vapor, resulting in a significant 23.17 % increase in the maximum power density (MPD) of the cell. To further enhance the performance of hydrazine hydrate fuel in PCFCs, a Pt–Al spherical catalyst is integrated within the anode structure of the cell. This approach notably improves the cell performance, yielding an additional 14.98 % increase in MPD. This design not only augments the electrical output but also effectively mitigates the degradation of the interface between the anode and the electrolyte. These optimization measures significantly improve the lifespan and reliability of the cell. The outcomes of this study demonstrate the practical feasibility of using hydrazine hydrate as a fuel in PCFCs.

Effect of composition gradient on detonation initiation in fuel-rich hydrogen-air mixtures in an obstructed channel

Numerical simulations were performed to study the effect of composition gradient and obstacle arrangement on detonation initiation in fuel-rich hydrogen-air mixtures. A third-order WENO method with adaptive mesh refinement (AMR) was used to solve the unsteady, fully-compressible, reactive Navier-Stokes equations coupled to a calibrated chemical-diffusive model (CDM). An obstructed channel at a blockage ratio of 0.3 filled with non-uniform hydrogen-air mixtures of an average H2 concentration 50 vol% was considered. The results show that unilateral obstacle arrangement is more conducive to flame acceleration (FA) and DDT than bilateral obstacle arrangement for both homogeneous and inhomogeneous mixtures. For inhomogeneous mixtures, the flame accelerates faster, and the detonation onset time is shorter when obstacles are placed on the sidewall with a hydrogen concentration closer to the stoichiometric ratio than the those when obstacles are placed on the other sidewall. However, the placement of unilateral obstacles on either the upper or lower sidewall does not significantly affect the DDT run-up distance. Besides, for fuel-rich inhomogeneous hydrogen-air mixtures, detonation tends to be initiated in the regions of high H2 concentration. Idealized models were introduced to simplify the intricate interactions of the reaction waves and flow fields to better understand the connection between H2 concentration distribution and detonation initiation. The analysis suggests that the minimum shock strength required for detonation initiation decreases with increasing equivalence ratio. This is supported by a kinetics analysis with detailed reaction model, which shows that ignition delay increases with decreasing equivalence ratio when detonation is about to be initiated.

Predicting the effect of cooling rates and initial hydrogen concentrations on porosity formation in Al‐Si castings

Predicting the effect of cooling rates and initial hydrogen concentrations on porosity formation in Al‐Si castings

Syngas Purpose Pyrolysis-Gasification of Organic Fractions of MSW over Metal-Loaded Y-Zeolite Catalysts

The increasing environmental consideration and the growth of instability of the energy market call for methods that can process the organic fraction of municipal solid waste (OFMSW) into fuel instead of disposal. Due to the pyrolysis and gasification that are efficient procedures to achieve valuable products, gasification of OFMSW with different particle sizes and compositions was carried out in the presence of Ni and Ni-Ce-loaded Y-zeolite in a multizone tubular kiln reactor. During the experiments, 500°C was applied in the first reactor zone, while the 2nd zone was at an elevated temperature of 600°C or 900°C in the presence of steam. The combined pyrolysis and gasification experiments were also carried out without a catalyst with the same operating conditions. The feedstock was collected from the organic fraction of a Hungarian mechanical-biological treatment (MBT) plant and was separated into four different fractions based on particle size: <1 cm dry biomass and fine particles, 1-2 cm paper-rich, 2-6 cm paper and plastic-rich feedstocks, and <6 cm mixture of these fractions. During the experimental work, product yields; gaseous product composition; the ratio of H2/CO, CO2/CO, and CH4/CO; and lower heating value were determined in the function of feedstock composition, the applied temperature, and catalysts. It was found that the hydrogen content and H2/CO ratio of gaseous products were increased due to catalyst application and temperature elevation in the 2nd reactor zone. The addition of Ce to the Ni/Y-zeolite catalyst was advantageous in the case of hydrogen formation at a lower temperature (600°C). The hydrogen and methane content of products obtained from the catalytic pyrolysis-gasification of paper and plastic-rich OFMSWs on elevated temperatures were higher, which increased the lower heating value of those products. Based on the elemental analysis of the obtained solid residues, it was found that paper/plastic-rich feedstock released hydrogen and carbon with a higher extent. 1-2 cm feedstock-related solid residues had the highest H/C ratio which caused a 12.5-12.8 MJ/kg gross heating value. As a result, combined pyrolysis and gasification appear to be an efficient method to attain valuable outputs from OFMSW not only in gas but also in solid products.

Design and Effect Evaluation of a Hydrogen–Natural Gas Mixing Device at Jingbian Compressor Station

Abstract Hydrogen gas is an environmentally friendly alternative energy source with zero emissions, making it highly valuable for replacing fossil fuels and reducing carbon emissions. One effective method of transporting hydrogen gas is by injecting it into existing natural gas pipelines. In this research, we focus on the Jingbian compressor station. This station is used for hydrogenation, blending hydrogen with the natural gas flowing through the pipelines. We propose a suitable process for hydrogen blending and design a mixing device to facilitate this process. To evaluate the mixing effect of the blended gas, we conducted numerical simulations to analyze the velocity and concentration distribution along the continuous section of the hydrogen blending pipeline. The results indicated that achieving a hydrogen branch length of 1/2 the diameter of the natural gas main pipe and a hydrogen flowrate of 10% resulted in a nonuniformity of hydrogen concentration at L = 30D of less than 0.05. Furthermore, when the hydrogen concentration was set at 3%, 10%, and 30%, the hydrogen concentration in the cross section of the pipe gradually approached the expected concentration as the mixed gas flowed. It is worth noting that during transportation of hydrogen-containing natural gas to the outlet, the velocity distribution on the cross section remained asymmetric, potentially leading to measurement errors. However, the use of a flow conditioner resulted in a further reduction in hydrogen nonuniformity and minimized velocity fluctuations, resulting in a small and uniformly distributed flow, which is advantageous for accurate measurement and transportation purposes.

The differences between the hydrogenation by means of photon-injection and electron-injection for N-type tunnel oxide passivated contacts solar cells

Tunnel Oxide Passivated Contact (TOPCon) solar cells have received widespread attention in recent years, especially in improving conversion efficiency. This paper investigated the impact of hydrogenation technology using photon-injection (HPI) and electron-injection (HEI) processes on TOPCon solar cells, highlighting the higher improvement effect and broader application scope of HPI compared to HEI. In TOPCon cells, several methods are available to prepare the tunneling oxide layer, such as plasma oxidation (PO) and indirect thermal oxidation (TO). The research results indicated that significant improvement differences could be observed when utilizing the HEI treatment for TOPCon solar cells prepared by PO and TO methods, with values of 0.133%abs. and −0.039%abs., respectively. Meanwhile, HPI treatment induced a more significant efficiency improvement for these two types of cells, and the increase in efficiency is 0.247%abs. and 0.244%abs., respectively. The experimental results demonstrated that the passivation effect for TOPCon solar cells prepared by PO and TO methods remained almost the same under the HPI treatment, and the improvement effect is less dependent on the tunnel oxidation technique used. Thus, the different passivation effects between HPI and HEI were further investigated, and the reason for the difference was attributed to the charge states and concentrations of hydrogen and non-equilibrium carriers during the hydrogenation. The results provided an improved scheme for enhancing the efficiency of TOPCon solar cells, shedding light on the role of HPI and HEI in the passivation process. This work brings further insights to TOPCon solar cells.

Dependence of a Hydrogen Buffer Layer on the Properties of Top-Gate IGZO TFT.

In this paper, the effect of a buffer layer created using different hydrogen-containing ratios of reactive gas on the electrical properties of a top-gate In-Ga-Zn-O thin-film transistor was thoroughly investigated. The interface roughness between the buffer layer and active layer was characterized using atomic force microscopy and X-ray reflection. The results obtained using Fourier transform infrared spectroscopy show that the hydrogen content of the buffer layer increases with the increase in the hydrogen content of the reaction gas. With the increase in the hydrogen-containing materials in the reactive gas, field effect mobility and negative bias illumination stress stability improve nearly twofold. The reasons for these results are explained using technical computer-aided design simulations.

Process Integration of Hydrogen Production Using Steam Gasification and Water-Gas Shift Reactions: A Case of Response Surface Method and Machine Learning Techniques

An equilibrium-based steady-state simulator model that predicts and optimizes hydrogen production from steam gasification of biomass is developed using ASPEN Plus software and artificial intelligence techniques. Corn cob’s chemical composition was characterized to ensure the biomass used as a gasifier and with potential for production of hydrogen. Artificial intelligence is used to examine the effects of the significant input variables on response variables, such as hydrogen mole fraction and hydrogen energy content. Optimizing the steam-gasification process using response surface methodology (RSM) considering a variety of biomass-steam ratios was carried out to achieve the best results. Hydrogen yield and the impact of main operating parameters were considered. A maximum hydrogen concentration is found in the gasifier and water-gas shift (WGS) reactor at the highest steam-to-biomass (S/B) ratio and the lowest WGS reaction temperature, while the gasification temperature has an optimum value. ANFIS was used to predict hydrogen of mole fraction, 0.5045 with the input parameters of S/B ratio of 2.449 and reactor pressure and temperature of 1 bar and 848°C, respectively. With the steam-gasification model operating at temperature (850°C), pressure (1 bar), and S/B ratio of 2.0, an ASPEN simulator achieved a maximum of 0.5862 mole fraction of hydrogen, while RSM gave an increase of 19.0% optimum hydrogen produced over the ANFIS prediction with the input parameters of S/B ratio of 1.053 and reactor pressure and temperature of 1 bar and 850°C, respectively. Varying the gasifier temperature and S/B ratio have, on the other hand, a crucial effect on the gasification process with artificial intelligence as a unique tool for process evaluation, prediction, and optimization to increase a significant impact on the products especially hydrogen.

Ultrasonication-induced metabolic pathway shifts and reduced electron carrier washout with biomass enhanced hydrogen yield in a continuous stirred tank reactor

Biohydrogen is pivotal for hydrogen economy, providing a renewable, carbon–neutral source of hydrogen from organic waste and biomass. It addresses environmental concerns and supports circular economy principles. However, challenges like managing metabolic pathways and dissolved hydrogen hinder attainment of higher hydrogen yields. This study explored the impact of organic loading rates (OLR) and ultrasonication on glucose fermentation by Clostridium pasteurianum for biohydrogen production.Results showed ultrasonication, particularly at 10 g/L.d OLR, increased hydrogen yield from 1.04 to 1.28 mol-H₂/mol-glucose. Higher OLR boosted biogas production, and at 10 g/L.d OLR, ultrasonication improved hydrogen purity from 46% to 53%, enhancing yield by 13%. C. pasteurianum shifted metabolic pathways under higher OLR, increasing lactate production to address redox imbalance. However, ultrasonication negatively affected lactate and acetate reutilisation, redirecting carbon flux from lactate to butyrate, increasing hydrogen yield.Combining ultrasonication and increased OLR enhanced glycolysis carbon flux by 14.5% and reduced biomass carbon flux by 10.5%. Hydrogen yield, influenced by glycolysis carbon flux, reached 82% under ultrasonication and increased OLR. Ultrasonication mitigated inhibitory effects on electron carrier molecule re-oxidation, emphasising the need to balance biomass, dissolved hydrogen concentration, and OLR for optimal hydrogen recovery.Despite decreased acetate/butyrate ratio and unchanged theoretical hydrogen production with ultrasonication, hydrogen yield increased. This likely resulted from reduced electron carrier molecule wastage with biomass, influenced by higher biomass concentration and ultrasonication. The study underscored preventing electron carrier molecule washout for higher hydrogen production and recommends using batch reactors over continuous stirred tank reactors in dark fermentation operations.

UV-visible spectroscopic investigations on the post-irradiation storage effect of polystyrene

Polystyrene is an electron-rich polymer wherein the electrons ejected on irradiation are localized and could be investigated by using spectroscopic methods. Pre-irradiated, PTPC (Pre-irradiated Tarsons Polystyrene Control) were irradiated with a cumulative dose of γ-rays 51, 77 and 129 kGy at 300-308 K referred to as RTPS (Re-irradiated Tarsons Polystyrene Samples). These RTPS were subjected to different post-irradiation treatments and were analyzed by UV-Vis absorption spectrometry. The regions 300 – 400 and 600 – 900 nm show differential absorption in RTPS in dose dose-dependent manner. The energy is absorbed by the phenyl chromophores of PS and redistributes the excitation energy. The data clearly suggests that RTPS (1mm) has retained its structural and chemical integrity as evidenced by UV-Vis spectrometry and hydrogen ion concentrations. The sterility was maintained for prolonged periods until packed properly facilitating the re-use multiple times before discarding. Though γ-irradiation has been in use for sterilization for a long time. The applications include the reusability of PS materials and evidence is provided for the structural and chemical integrity after re-irradiation. This method is cost-effective for biological laboratories and environmentally friendly.

Hydrogen in natural diamond: Quantification of N3VH defects using SIMS and FTIR data

A set of ten diamonds from different sources representing the main types of physical classification (IaA, IaAB, IaB and IIa) has been first explored by FTIR spectroscopy and SIMS calibrated by hydrogen ion implantation. The concentrations of hydrogen in the studied diamonds measured by SIMS range between 9.98 and 47.6 at.ppm or from 1.76 × 1018 to 8.40 × 1018 at./cm3. The 3107 cm−1 absorption line has been detected by FTIR spectroscopy (resolution near 1 cm−1) in five studied diamonds (IaB and IaAB). The 3107 cm−1 IR absorption lines due to H defects in these diamonds have been successfully described by the Lorentzian shape and their parameters have been evaluated. Based on the linear regression equation relating intensities of the 3107 cm−1 IR absorption lines in the studied diamonds with their H defect concentrations, the H defect IR absorption at 3107 cm−1 in diamond has been quantified. The absorption calibration constant for diamond's 3107 cm−1 absorption line is 386 ± 64 ppb cm2. The corresponding cross-section per one H defect σ3107 (cm2) = (9.34 ± 1.25) × 10−18 /Γ (cm−1), Γ is the full width at half maximum (FWHM) of the 3107 cm−1 absorption line. Based on a widely accepted interpretation that the H defect resulting in the 3107 cm−1 IR absorption peak in diamonds is the N3VH defect, the values of the obtained calibration constant and cross-section have been assigned to the N3VH defect in diamond. The equations relating concentration of the N3VH defect ([N3VH]) with the 3107 cm−1 IR absorption line integrated intensity (I3107) and intensity (α3107) are as follows: [N3VH] (ppb) = (386 ± 64) I3107; [N3VH] (ppm) = (0.607 ± 0.080) α3107 (cm−1)Γ (cm−1). Hydrogen impurities that do not contribute to the IR absorption at the 3107 cm−1 peak were detected in all studied diamonds.

Design of hydrogen embrittlement resistant 7xxx-T6 aluminum alloys based on wire arc additive manufacturing: Changing nanochemistry of strengthening precipitates

In this work, atom probe tomography technique is used to investigate how wire arc additive manufacturing (WAAM) changes the nanochemistry of nanoprecipitates and grain boundaries after peak aging of a high strength Al-Zn-Mg-Cu alloy. The effect of the change in nanochemistry of nanoprecipitates on the hydrogen embrittlement of the additively manufactured aluminum alloy is investigated using a three-point bending test in humid air. The results show that the unique in-process heat treatment during WAAM, offers the possibility to modify the nanochemistry of nanoprecipitates and improve the resistance to hydrogen embrittlement of the Al-Zn-Mg-Cu alloys in the peak aged state without sacrificing mechanical performance. Density functional theory shows that the WAAM process transforms the interfaces between matrix and precipitate into a strong hydrogen trap, which can reduce the hydrogen content of grain boundaries and suppress hydrogen-induced intergranular fracture.

Multiple carbonate system parameters independently govern shell formation in a marine mussel

Calcification is vital to marine organisms that produce calcium carbonate shells and skeletons. However, how calcification is impacted by ongoing environmental changes, including ocean acidification, remains incompletely understood due to complex relationships among the carbonate system variables hypothesized to drive calcification. Here, we experimentally decouple these drivers in an exploration of shell formation in adult marine mussels, Mytilus californianus. In contrast to models that focus on single parameters like calcium carbonate saturation state, our results implicate two independent factors, bicarbonate concentration and seawater pH, in governing calcification. While qualitatively similar to ideas embodied in the related substrate-inhibitor ratio (bicarbonate divided by hydrogen ion concentration), our data highlight that merging bicarbonate ion and hydrogen ion concentrations into a simple quotient obscures important features of calcification. Considering a dual-parameter framework improves mechanistic understanding of how calcifiers interact with complex and changing chemical conditions.