Low Oxygen Concentrations Research Articles

Catalytic Valorization of Organic Solid Waste: A Pilot-Scale Run of Sugarcane Bagasse

Organic solid waste treatment is crucial for enhancing environmental sustainability, promoting economic growth, and improving public health. Following our previous organic solid waste upgrading technique, a further two-step pilot-scale run, using sugarcane bagasse as the feedstock, has been successfully conducted with long-term stability. Firstly, the sugarcane bagasse was treated under mild conditions (400 °C and 1 bar of CH4), and this catalytic Methanolysis treatment resulted in a bio-oil with a yield of 60.5 wt.%. Following that, it was subjected to a catalytic Methano-Refining process (400 °C and 50 bar of CH4) to achieve high-quality renewable fuel with a liquid yield of 95.0 wt.%. Additionally, this renewable fuel can be regarded as an ideal diesel component with a high cetane number, high heating values, a low freezing point, low density and viscosity, and low oxygen, nitrogen, and sulfur contents. The successful pilot-scale catalytic upgrading of sugarcane bagasse further verified the effectiveness of this methane-assisted organic solid waste upgrading technique and confirmed the high flexibility of this innovative technology for processing a wide spectrum of agricultural and forestry residues. This study will shed light on the further valorization of organic solid waste and other carbonaceous materials.

Whole transcriptome sequencing revealed the gene regulatory network of hypoxic response in yak Sertoli cells

Yaks live in the Qinghai-Tibet Plateau for a long time where oxygen is scarce, but can ensure the smooth development of testis and spermatogenesis. The key lies in the functional regulation of the Sertoli cells under hypoxia. In this study, we sequenced yak Sertoli cells cultured in normal oxygen concentration (Normoxia) and treated with low oxygen concentration (Hypoxia) by whole transcriptomics, and screened out 194 differentially expressed mRNAs (DEmRNAs), 934 differentially expressed LncRNAs (DELncRNAs) and 129 differentially expressed miRNAs (DEmiRNAs). GO and KEGG analysis showed that these differential genes were mainly concentrated in PI3K-AKT, MAPK, RAS, and other signaling pathways, and were associated with glucose metabolism, tight junction, steroid hormone synthesis, cell fusion, and immunity of yak Sertoli cells. We constructed the gene interaction network of yak Sertoli cells in hypoxia and screened out the relationship pairs related to glucose metabolism and tight junction. The results suggested that the changes in energy metabolism, tight junction, and immune regulation of yak Sertoli cells under hypoxia might provide favorable conditions for spermatogenesis. This study provides data for further study on the role of non-coding RNA in testis development and spermatogenesis of yak.

ГИПОКСИЯ И АНОКСИЯ В ГДАНЬСКОЙ ВПАДИНЕ БАЛТИЙСКОГО МОРЯ В 2021–2023 гг.

The central part of Gdansk Deep experienced summer-autumn dissolved oxygen minima within 2021–2023, while along the periphery of the Deep no seasonality was detected. Intrusions of transformed North Sea waters with a low oxygen content can partially aerate the bottom layer and cause anoxic waters to detach from the bottom. In the near-slope southeastern part of the Deep, in autumn-winter storm conditions, amplitude vertical fluctuations in oxygen concentration can occur – from the rise of hypoxic waters above the halocline, to the complete elimination of hypoxia as a result of near-slope downwelling, which acts as an “oxygen pump”. The hydrological and hydrochemical characteristics of intrusions of transformed North Sea waters penetrating into the Gdansk Basin and influencing the dynamics of the nepheloid layer of biogeochemical origin, arising at the boundary of oxidizing and reducing conditions, have been clarified.

The Comparative Impact of Liberal Versus Conservative Oxygenation in Critically Ill COVID-19 Patients: A Retrospective Study.

Objectives Whether a higher or lower partial pressure of oxygen (PaO2) could impact outcomes in patients with coronavirus disease 2019 (COVID-19) remains a matter of debate. So, we planned this retrospective analysis to determine if a higher or lower partial pressure of oxygen in blood had any effect on outcomes in COVID-19 patients. Material and method The records of COVID-19 patients from the beginning of 2020 to the end of 2022 were scanned. Patients were sub-grouped into two groups based on the partial pressure of oxygen (PaO2) values on arterial blood gas (ABG), i.e., high PaO2group,PaO2 value of 80-100 mm Hg, and low PaO2group,PaO2 value of 60-80 mm Hg for the first 48 hours after the initiation of oxygenation and/or mechanical ventilation. The two groups were compared in terms of partial pressure of oxygen in arterial blood to the fraction of inspiratory oxygen (FiO2) concentration (P/F ratio), Sequential Organ Failure Assessment (SOFA) score at presentation and after 48 hours, and clinical outcomes, including mortality, time of mortality, extubation, acute kidney injury (AKI), and change in Glasgow Coma Scale (GCS). Results SOFA score was significantly higher in the low PaO2 group as compared to the high PaO2 group both at baseline (4.59 {1.79} versus 5.51 {1.15}; p-value: 0.005) and at 48 hours (3.06 {1.39} versus 5.11 {2.13}; p-value: 0.007). However, the change in SOFA score over 48 hours did not achieve statistical significance (-1.000 {0.97} versus 0.53 {2.34}; p-value: 0.257). Out of a total of 37 patients, 21 patients died in the high PaO2 group, while 18 patients died in the low PaO2 group. Conclusion Our study highlights that targeting either low or high arterial oxygen content while considering oxygen therapy for COVID-19 patients did not significantly alter the outcomes.

Conversion of soybean oil under subcritical water conditions into liquid biofuels with low oxygen contents

Although the hydrotreatment of natural triglycerides is a well-established route for producing sustainable aviation fuel and renewable diesel, its high hydrogen consumption is a concern. The hydrothermolysis of natural triglycerides is considered a highly promising alternative route; however, the correlation between process parameters and fuel properties and detailed chemical structures of the produced fuel have not been established. Herein, we investigated the conversion of soybean oil to gasoline-, jet fuel- and diesel-fraction hydrocarbons with low oxygen contents. The properties of fuels produced under various reaction conditions were analyzed comprehensively using simulated distillation, total acid number (TAN), and elemental analysis. Under the optimized reaction conditions of 420 °C, 4.5 MPa, an oil-to-water ratio of 6:1, and reaction time of 10 min, 26 % gasoline-, 62 % jet fuel-, and 90 % diesel-range hydrocarbons with a low oxygen content of 5.1 %, low TAN of 0.04 mg KOH g−1, and high calorific value of 42.7 MJ kg−1 resulted. To elucidate the reaction mechanism, the liquid products produced from soybean oil were analyzed using comprehensive two-dimensional gas chromatography combined with time-of-flight mass spectrometry. In addition, based on the oleic acid conversion under varying hydrothermal conditions, we proposed deoxygenation, cracking, cyclization, and aromatization pathways. The findings of this study present possibilities for producing sustainable biofuels with low oxygen contents for the aviation industry.

Three-dimensional-electrode Electrochemical Oxidation of Refractory Organic Matter in a Cold High-altitude Area: A Case Study of Dibutyl Phthalate

Qinghai has a high altitude, low average temperature and low oxygen concentration, but it has abundant power resources, so it has a good application prospect to use electrochemical oxidation to degrade refractory organic matter. In this study, a three-dimensional electrode electrochemical oxidation system was constructed with powdered activated carbon as the particle electrode, graphite as the anode and stainless steel as the cathode, and the electrochemical oxidation degradation effect of DBP simulated wastewater at high altitude was studied. When applying the system to the simulated wastewater, the maximum chemical oxygen demand (COD) removal rate reached 61.75% at a plate spacing of 5 cm, electrolyte and particle-electrode dosages of 12 g and 35 g, respectively, and an electrolytic voltage of 20 V. Electrolyte voltage is the most influential factor in the COD removal rate, followed by plate spacing, electrolyte dosage, and particle electrode dosage. The graphite electrode was confirmed to be higher-value than ruthenium–iridium, titanium mesh, and lead dioxide electrodes.

Unraveling NO Production in N2-O2 Plasmas with 0D Kinetic Modeling and Experimental Validation.

This work presents a detailed investigation aimed at understanding the key mechanisms governing nitric oxide (NO) production in N2-O2 discharges by systematically comparing experimental results to modeling data. The experimental phase capitalizes on radiofrequency (13.56 MHz) discharges, sustained at 5 mbar pressure conditions, featuring varying concentrations of oxygen, ranging from pure N2 plasma to air-like mixtures. On the modeling front, we adopt an integrated approach that combines the solution of the Boltzmann equation for electrons with a system of rate balance equations for heavy species. To account for ground state NO(X) generation at the reactor wall, we combine the volume chemistry with a mesoscopic description of the surface, taking into account adsorption sites and various elementary surface phenomena. Comparisons between experiments and modeling demonstrate very good agreement, extending beyond NO(X) formation to encompass other species in the plasma such as N2O(X) and atomic nitrogen N(4S). Noteworthy findings include (i) the pivotal role of surface mechanisms in NO(X) production, particularly at low oxygen content values; (ii) the significance of accurately describing the postdischarge phase, where depletion of plasma species occurs at different time scales (millisecond range); and (iii) the importance of vibrationally and electronically excited states (e.g., O2(b)) in elucidating NO(X) formation dynamics, crucial for unraveling reaction pathways and energy transfer processes. This work makes an important step toward formulating a comprehensive reaction mechanism for N2 and N2-O2 plasmas applied to nitrogen fixation, covering both volume and surface mechanisms, and lays a robust foundation for future research on plasma-based NO(X) production, particularly in the presence of catalysts.

Recycling of reduced graphene oxide from graphite rods in disposable zinc battery applicable to optical sensing

We report a low cost, simple method to fabricate reduced graphene oxide (rGO) optical sensors from recycled batteries. The rGO nanosheets were exfoliated by electrochemical method under the assistant of electric arc using 5 % KOH or NaOH electrolytes. The rGO nanosheets show interlayer distances ranging from 3.98 to 6.22 Å, and thicknesses from 0.62 to 6.00 nm, corresponding from 1 to 10 layers, respectively, determined from X-ray diffraction (XRD), atomic force microscopy (AFM), and transmission electron microscopy (TEM) measurements. Selected area electron diffraction (SAED) measurement indicates that rGO nanosheets content Miller-Bravais indices of (1–210) and (0–110) planes, and the hexagonal diffraction pattern of (0–110) plane of graphene sheets with d-spacing of 2.13 Å. Low defect densities in exfoliated rGO nanosheets were confirmed by ID/IG ratios ∼0.16 to 0.18 via Raman. The rGO nanosheets exfoliated in NaOH electrolyte have 19.35 % lower oxygen content compared to those exfoliated in KOH electrolyte inspected from XPS spectra. The performance of the rGO optical sensors is controlled by defects created from oxygen functional groups formed during exfoliation process. The responsivity and response (rise) time of NaOH-exfoliated rGO sensor are 0.46 A/W and 2.3 s, respectively. These values are 21 % (for responsivity) larger and 35 % (for rise time) smaller than those of KOH-exfoliated rGO sensor. The best-in-class of high gain were demonstrated in this study for the rGO optical sensors prepared from disposed graphite rods. The results demonstrate how disposed batteries can be recycled to produce photodetectors and other optoelectronic devices using cheap and relatively nontoxic methods.

Mono-and bi-metal catalytic hydrothermal liquefaction of food waste: Screening the process parameter on product yield and characterizations

Biofuels and chemicals derived from wet food waste (FW) can serve as a strategy to significantly reduce emissions and mitigate environmental pollution while preventing the loss of valuable resources. Hydrothermal liquefaction (HTL) is one of the most promising thermochemical techniques for converting wet waste into crude oil-like products (biocrude). In this study, catalytic HTL of FW was carried out using cobalt (Co), magnesium (Mg), and cobalt-magnesium (Co–Mg) supported on ZSM-5 to produce high-quality biocrude. The impact of key operating parameters, such as reaction solvent, temperature, reaction holding time, and catalyst amount, was investigated. In comparison to non-catalytic liquefaction, catalytic liquefaction significantly improved the biocrude yield. The maximum biocrude yield (60.89 wt%) was achieved with bimetallic Co–Mg/ZSM-5 catalysts at 280 °C with 10 wt% of catalyst at a reaction time of 15 min. Various analytical methods, including GC-MS, FT-IR, CHNS, TGA, and NMR, were employed to identify the composition and quality of the biocrudes. Catalytic liquefaction with Co–Mg/ZSM-5 in an ethanol solvent resulted in a higher percentage of ester compounds (74.15%, area percentage). The biocrude obtained through the catalytic process had lower oxygen and nitrogen content, which led to a higher heating value (HHV). Biocrude quantification revealed the presence of 12.16 wt% of linoleic ester compounds. The concentration of total nitrogen (TN) in the catalytic aqueous phase was as high as 2.44 g/L, significantly greater than the 0.32 g/L found in the non-catalytic aqueous phase. Furthermore, the optimum Co–Mg/ZSM-5 catalyst demonstrated excellent reusability and stability in FW liquefaction.

Parameter optimization of ultrafine molybdenum powder during hydrogen reduction of MoO2 based on central composite design method

The hydrogen reduction of MoO2 is a common method for preparing ultrafine molybdenum powder, which is an important basic material for manufacturing high-performance Mo-based alloys. However, its preparation parameters are usually hard to be controlled. To address this issue, the work conducted the parameter optimization research during the hydrogen reduction process with using central composite design method, and the influence of different parameters such as reaction temperature, yttrium content, and hydrogen flow rate, on the particle size and oxygen content of the prepared molybdenum powder were investigated. The findings showed that the particle size of the prepared molybdenum powder is gradually decreased with the increase of reaction temperature and yttrium content, while gradually increased with the increase of hydrogen flow rate. The oxygen content of the prepared molybdenum powder is gradually decreased with the increase of reaction temperature and hydrogen flow rate, while gradually increased with the increase of yttrium content. Reaction temperature and yttrium content have significant interactions on the particle size and oxygen content are also concluded, and their respective regression model equations are obtained. The result also demonstrated that the particle size and oxygen content of the prepared molybdenum powder had a certain contradictory relationship. Through the comprehensive analysis, the optimal parameters for preparing ultrafine molybdenum powder with a low oxygen content are deduced, that is, reaction temperature: 1200 K, yttrium content: 0.1 mass%, and hydrogen flow rate: 1000 mL/min. Under the conditions, the average particle size and oxygen content of the prepared molybdenum powder are 320 nm and 0.456 mass%, respectively.

JrPPO1/2 play distinct roles in regulating walnut fruit browning by different spatiotemporal expression and enzymatic characteristics

Polyphenol oxidase (PPO) activity drives walnut fruit browning, but the roles of its only two-family genes, JrPPO1 and JrPPO2, remain unclear. This study explores the spatiotemporal expression and enzymatic characteristics of JrPPO1 and JrPPO2 in walnut. Treatment with the PPO activator CuSO4 and H2O2 accelerated fruit browning and up-regulated JrPPO1/2 expression, whereas treatment with the PPO inhibitor ascorbic acid delayed browning, down-regulating JrPPO1 and up-regulating JrPPO2 expression. Compared to mJrPPO1, mJrPPO2 can exhibited better enzyme activity at higher temperatures (47 °C) and in more acidic environments (pH 4.25). mJrPPO2 exhibited a higher substrate specificity over mJrPPO1, and the preferred substrates are catechol, chlorogenic acid, and epicatechin. Additionally, mJrPPO2 adapted better to low concentration of oxygen (as low as 1.0% O2) and slightly elevated CO2 levels compared to mJrPPO1. Subcellular localization and spatiotemporal expression patterns showed that JrPPO1 is only expressed in green tissues and located in chloroplasts, while JrPPO2 is also located in chloroplasts, partly associated with membranes, and is expressed in both green and non-green tissues. Silencing JrPPO1/2 with virus-induced gene silencing (VIGS) reduced fruit browning, maintained higher total phenols, and decreased MDA production. Notably, silencing JrPPO1 had a greater impact on browning than JrPPO2, indicating JrPPO1's greater contribution to PPO activity and fruit browning in walnut fruits. Consequently, JrPPO1 can be effectively regulated both at the molecular level and by manipulating environmental conditions, to achieve the objective of controlling fruit browning.

Plasma-Enhanced Copper Sulfide/Oxide Electrode for Zinc-Air/Copper Dual Mode Battery

As search for novel electrochemical energy storage systems continues, metal-air batteries are one of the possible solution. Consisting of a metal anode and an air-breathing cathode, by design, they achieve much higher gravimetric energy density in theory. However, s-orbital metals suffer passivation issues and poses safety threats due to their reactivity with air and humidity. As a solution to this issue, safer d-block metals are being studied as an alternative. Zinc air batteries (ZABs) utilizes earth-abundant and cost-effective zinc as its anode, and has high theoretical capacity. At its cathode, oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) occur during charging and discharge processes. Sluggish kinetics of ORR degrades the discharge performance, and is the bottleneck in commercial application of the zinc air battery. Additionally, irreversibility of the cathode reaction results in dissatisfactory retention of battery capacity. Current state-of-the-art noble metal catalysts achieves nearly 80% of the theoretical capacity. However, its cycling stability is severely limited to less than 200 cycles despite low discharge rate applied.Herein, we present a nitrogen plasma-enhanced copper sulfide/oxide catalyst (referred to as N-CuS) that exhibits good catalytic activity for its application as the air-breathing cathode for ZABs. The material is grown directly on metal foam surface using anodization, which is then treated using nitrogen plasma. Anodization creates defect-rich flakes of copper sulfide on the oxide surface, highly increasing surface area and creating the active sites. The material has good electrical conductivity and highly open porous structure that alleviates mass transport issues. Additionally, nitrogen plasma treatment further increases the surface area about 80%, and is expected to introduce nitrogen dopants to the surface, enhancing conductivity of the material. ECSA estimated by measuring Cdl shows that each process increases the ECSA by over 40 times and about 1.8 times, respectively.LSV of CuS and N-CuS half-cells have been performed to measure and compare catalytic performance of the material. N-CuS shows far higher current density and better catalytic activity (35mV less overpotential) than CuS, and higher output voltage is observed with N-CuS cells with the same current density. By assessing the GCPL (potential limited galvanostatic cycling) results, it was concluded that N-CuS requires lower charging voltage and exhibits higher discharge voltages than CuS.The overall performance was evaluated in a stack cell configuration, utilizing thin zinc foil as its anode to minimize mass error. The measured specific capacity of the cell was 789.3 mA·h·g-1, which approximately is 85% of the theoretical specific capacity of zinc-air cells (820 mA·h·g-1). This cell yields gravimetric energy density of about 666 Wh·kg-1. It is notable that these ZAB characteristics are comparable to Pt/C, the state-of-the-art catalyst as of now. N-CuS may be a viable replacement for the Pt/C electrode, resulting in the cost-saving effect. The cycling stability of both N-CuS and Pt/C-based ZAB has been assessed to show that N-CuS-based ZAB has much prolonged (more than twice the cycles) cyclability compared to Pt/C-based ZAB (Fig. S11).Additionally, ZAB constructed using N-CuS can operate in oxygen-deficient environments. As the counter reaction it utilizes redox reaction of copper oxides (Zn-Cu mode) in the substrate when operating in anaerobic conditions. The reduction of divalent and monovalent copper oxides appears as plateaus at 1.1 V and 0.8 V versus the zinc anode during GCPL. Due to this alternate reaction, the cell can operate even at low concentrations of oxygen or even in its absence.DFT calculations have been performed to elucidate the reaction mechanism and the intrinsic catalytic activity of the material, and shows nitrogen dopants improve reactivity of the active sites, thus reducing the overpotential.In summary, we have synthesized N-CuS as the OER/ORR catalyst for ZAB. Through anodization the catalyst was directly grown on the substrate and nitrogen plasma treatment further enhances the catalyst properties to render it higher surface area, conductivity, and better stability. This allows better reversibility in the OER/ORR and results in enhanced cyclability of the overall cell. The constructed RZAB exhibited high specific capacity of 789.3 mA·h·g-1, which, has higher capacity than the analogue using Pt/C catalyst. In addition, N-CuS based RZAB is capable of operating under oxygen-deficient conditions utilizing the metal oxide substrate. This allows the dual mode operation of zinc-air and zinc-copper modes, and results in a more consistent output from the RZAB, as short-term air supply issues could be buffered by this effect. Figure 1

AN ADVANCED APPROACH TO THE DEFINITION OF THE “MILKY WAY GALAXIES-ANALOGUES”

Our Galaxy — the Milky Way — has certain features of the structure and evolution. The morphological, photometric, kinematic, and chemodynamical properties are usually considered in search for the Milky Way galaxies-analogues (MWAs). The discovery of MWA galaxies with a larger number of simultaneous selection parameters, as well as more stringent constraints on a given parameter, yields a sample of MWA galaxies with properties closer to the true properties of the Milky Way. So, in general, such MW parameters as the morphological type, luminosity, color indices, structural parameters (size, bar, bulge, thin and thick disks, inner ring, halo), bulge- to-total ratio, stellar mass, star formation rate, metallicity, and rotation velocity were used in various combinations for comparison with other galaxies. However, the offset of some MW features in the multi-parameter space of MWAs features should be significant. The paper aims to give a brief overview of the problematics and to present our approach for studying Milky Way and MWAs match- ing characteristics (this project is supported by the National Research Fund of Ukraine). We propose to enlarge as much as possible the number of Milky Way features and compile various samples of MWAs in our co-moving cosmological volume for their further optimization. Such features can include 3D-kinematics of star’s movement in certain regions, low oxygen content on the periphery, low nuclear activity, and the lack of significant merging over the past 10 Gyrs (isolation criterion). This approach will make it possible to widely formulate the necessary and sufficient conditions for the detection of MWA galaxies as well as to reveal other MW multiwave- length features

The Role of Oxygen on Defects Formation during Advanced Silicon Process Technologies

Impact of oxygen in silicon substrates and the formation of oxide precipitates have been widely studied in the past because of the detrimental electrical recombination and its effect on yield [1,2]. The origin of interstitial oxygen (Oi) is not only limited to the substrate but also comes from the nature of the oxide that may be deposited on it [3]. Interstitial oxygen plays a direct role in the formation of bulk microdefects (BMDs) resulting from oxygen precipitation during low-temperature Front-End anneals at 650-800°C [4,5]. The latter are of interest for the mechanical robustness of substrates, contributing to the pinning of slip lines (SL) and for the reliability of devices thanks to an internal gettering effect, but can also be harmful by emitting dislocations when they are too numerous (> 1 x 1010 BMD.cm-3) [5, 8].In this paper, we have reviewed the different impacts of interstitial oxygen on silicon substrates during thermal annealing through 3 phenomena: (i) the influence of Oi on the reduction of the slip lines by the pinning effect, (ii) the formation of BMDs induced by Oi and their interactions with dopants during implantation processes, (iii) the BMDs limited formation in the specific case of high resistivity (HR) silicon substrates. We focused on standard and high resistivity silicon substrates obtained by Czochralski (CZ) method, used in advanced technologies for various applications (digital, bipolar, power, photonic, etc.).To highlight the impact of interstitial oxygen, firstly on the mechanical properties of substrates, we studied the same p-type silicon substrates with two ranges of Oi concentration (5.33 x 1017 and 7.23 x 1017 at.cm-3), both annealed by furnace oxidation below 1000°C and N2 annealing above 1000°C. Figure 1 clearly shows the effect of a minor difference in Oi concentration on the number of slip lines detected by Pattern Wafer Geometry (PWG) measurements (Figure 2). Despite extrinsic process parameters to consider in the occurrence of slip lines, these results demonstrate the enhancement of slip line pinning by interstitial oxygen.Bulk microdefects in silicon are known to interact with dopants [6]. To investigate this point, we compared the BMD occurrence in non-implanted and antimony-implanted (2 x 1015 at.cm-2) silicon substrates using micro-photoluminescence imaging. These substrates contain relatively high Oi concentrations (up to 6.7 x 1017 at.cm-3) and have been subjected to oxidation and rapid thermal annealing (RTA) above 900°C. After adjusting for background contrast in the implanted and non-implanted regions, Figure 3 shows different trends in BMD density evolution as a function of the probed depth. We assume that a mechanism based on a mechanical stress field induced by the position of the Sb-implanted atoms in the lattice limits the nucleation of oxide precipitates [7]. However, further characterization methods are required to confirm the influence of dopants on the BMD density.Finally, high resistivity silicon substrates are being considered to significantly improve devices performance, particularly in high frequency and photonics applications [8, 9]. However, the understanding of BMD formation is poorly documented in the literature. These CZ-Si substrates are characterized by low oxygen content (< 3 x 1017 at.cm-3) and low boron dopant concentration (< 1 x 1014 at.cm-3). At such low values, the expected oxygen precipitation is very different from that of standard p-type silicon [8, 10]. We investigated the effect of these parameters on BMD formation through precipitation thermal treatments (N2 + O2 anneal > 1000°C). Figure 4 illustrates the important difference in BMD formation depending on the substrate characteristics (standard resistivity high-Oi versus high resistivity low-Oi silicon) after the same thermal treatment. BMD defects were generated in large quantities in standard silicon (3 x 109 BMD.cm-3), whereas no BMDs were observed in HR silicon.In summary, we have demonstrated the impact of interstitial oxygen (coming from substrates and processes) on defect generation, particularly BMD, in silicon technology. In controlled proportions, they play an important role in the proper functioning of devices and very often result from the fine tuning between substrate characteristics and process conditions.[1] Jun Fujise et al 2018 JJAP. 57 035501[2] Zijing Wang et al 2022 APE 15 071004[3] G. Kissinger et al 2019 ECS J3ST. 8 N79[4] Maria Porrini et al 2018 ECS Trans. 86 7[5] Hirofumi Shimizu et al 1985 JJAP. 24 815[6] Hideki Tsuya et al 1983 JJAP. 22 L1[7] Oleksandr Oberemok et al 2014 PSS. 11 163439[8] Isabelle Bertrand et al 2022 ECS Trans. 31 108[9] Jarosław Judek et al 2017 JEM. 46 5589-5592[10] Kaoru Kajiwara et al 2019 PSS. 17 216 Figure 1

Hypoxia-inducible factors in postnatal mouse molar dental pulp development: insights into expression patterns, localisation and metabolic pathways.

Hypoxia is relevant to several physiological and pathological processesand this also applies for the tooth. The adaptive response to lowering oxygen concentration is mediated by hypoxia-inducible factors (HIFs). Since HIFs were shown to participate in the promotion of angiogenesis, stem cell survival, odontoblast differentiation and dentin formation, they may play a beneficial role in the tooth reparative processes. Although some data were generated in vitro, little is known about the in vivo context of HIFs in tooth development. In order to contribute to this field, the mouse mandibular first molar was used as a model.The expression and in situ localisation of HIFs were examined at postnatal (P) days P0, P7, P14, using RT-PCR and immunostaining. The expression pattern of a broad spectrum of hypoxia-related genes was monitored by customised PCR Arrays. Metabolic aspects were evaluated by determination of the lactate level and mRNA expression of the mitochondrial marker Nd1.The results show constant high mRNA expression of Hif1a, increasing expression of Hif2a, and very low expression of Hif3a during early postnatal molar development. In the examined period the localisation of HIFs in the nuclei of odontoblasts and the subodontoblastic layer identified their presence during odontoblastic differentiation. Additionally, the lower lactate level and higher expression of mitochondrial Nd1 in advanced development points to decreasing glycolysis during differentiation. Postnatal nuclear localisation of HIFs indicates a hypoxic state in specific areas of dental pulp as oxygen demands depend on physiological events such as crown and root dentin mineralization.

Evaluation of the properties of bio-asphalt derived from waste cooking oil and low-density polyethylene through the pyrolysis process

The aim of this study is to prepare a bio-asphalt for flexible pavement construction using a fixed-bed pyrolysis reactor. This method involves incorporating waste cooking oil (WCO) and low-density polyethylene (LDPE) as feedstock materials. Through this study, an attempt has been made to make use of waste materials and promote the use of environmentally friendly binders in sustainable road construction. The pyrolysis experiment was conducted at different temperatures, varying from 250 °C to 500 °C for different blends of waste cooking oil (WCO) and low-density polyethylene (LDPE), i.e., 1:0, 3:1, 1:1, 1:3, and 0:1, respectively. At a temperature of 350 °C, the pyrolysis process is more effective for converting various blends of waste cooking oil (WCO) and low-density polyethylene (LDPE) into bio-asphalt. The maximum bio-asphalt yield of 82 wt% was reported for the 1:3 blend at a temperature of 350 °C. The elemental analysis of an equal mass of waste cooking oil (WCO) and low-density polyethylene (LDPE) reported a carbon content of 83.93 wt%, a hydrogen content of 13.29 wt%, and a lower oxygen content of 2.55 wt%. The Gas Chromatography Mass Spectrography (GC-MS) analysis indicated the presence of chemical compounds such as pentadecane, heptadecane, dodecane, cyclopentylpropyl, and hexacosene in the 1:1 blend. The thermogravimetric and derivative thermogravimetric analyses indicate that the 1:1 blend and 1:3 blend can withstand temperatures around 473 °C and 475 °C, respectively. The Fourier transform infrared spectroscopy (FT-IR) analysis showed the presence of alkane, alkene, ester, and other aromatic compounds. Based on this present study, it has been noted that the chemical composition of a 1:1 blend of waste cooking oil (WCO) and low-density polyethylene (LDPE)-based bio-asphalt contains similar chemical compositions as asphalt binder, and it can be used as a modifier for conventional asphalt binder.

Catalytic pyrolysis of apricot kernel shell over metal supported MCM-41 catalysts obtained by synthesizing sonochemical method

In this study, it is targeted to examine the efficiency of metal supported MCM-41 catalysts on the liquid product yield from pyrolysis process of apricot kernel shell selected as a biomass and to characterize the pyrolysis liquids. In the non-catalytic pyrolysis experiments, the maximum liquid yield is obtained as 21.41 % at 500 °C. At the determined optimum condition, catalytic pyrolysis process of the biomass sample is performed with metal supported MCM-41 catalysts synthesized by sonochemical method (metal: aluminium, cobalt, iron) at different ratios to biomass (1 and 2 wt %). The pyrolysis procedures of apricot kernel shell are carried out in a tubular fixed-bed reactor at different pyrolysis temperatures. The use of catalysts improved both the liquid product (tar) yield and tar quality in respect to the calorific value, the distribution of hydrocarbons and the elimination of oxygenated groups. The results revealed that all metal-supported MCM-41 catalysts, especially the Fe-MCM-41 catalyst ratio of 2, showed an excellent catalytic ability for thermal conversion of biomass. In the catalytic pyrolysis experiments carried out at 500 °C, 75.84 % conversion to liquid and gaseous products was obtained using 2 % Fe-MCM-41 catalyst, and the calorific value of the liquid product obtained was determined as 40.96 MJ/kg. The functional group analyses in the structure of the liquid products are characterized using FT-IR spectroscopy, and the distributions of the aliphatic/aromatic fractions of the liquid products are characterized using GC-MS technique. The H/C ratio of the liquid product obtained from catalytic pyrolysis is between light and heavy petroleum products and also has lower oxygen content and higher calorific value, indicating the potential of metal-supported MCM-41 catalyst for renewable hydrocarbon production from apricot kernel shell.

Influence of methane-oxygen coupled gas field on the transformation mechanism of microporosity and active structure of cryogenic pre-oxidized residual coal

Due to the impact of coal seam mining processes and the release of adsorbed gases in residual coal, a mixed gas field of methane and oxygen is formed in the goaf, which affects the oxidation process of the residual coal over a long period. In this study, to explore the low-temperature oxidation mechanism of residual coal in a hypoxic methane-containing environment, Low temperature nitrogen adsorption (LTNA) experiments and Fourier transform infrared spectroscopy (FTIR) were utilized to examine the pore development properties of residual coal and the transformation mechanisms of reactive micro-groups. The results indicate that increases in temperature and methane proportion promote the transition of various pores to larger scales, with 3 % methane inducing the formation of fine micropores, thereby increasing the specific surface area of the coal. High temperatures (80℃，100℃) and increased proportions of oxygen and methane synergistically elevate the fractal dimensions. Methane inhibits the consumption of hydroxyl groups, and a low oxygen concentration (5 %) impedes the gas production from coal oxidation. The presence of both oxygen and methane exhibits a compound effect; the strongest tendency towards spontaneous combustion occur at 1 % methane and 9 % oxygen. The findings provide valuable insights for controlling spontaneous combustion disasters in goafs.

Hypoxia related genes modulate in similar fashion in skin fibroblast cells of yak (Bos grunniens) adapted to high altitude and native cows (Bos indicus) adapted to tropical climate during hypoxia stress.

The present study was conducted to understand transcriptional response of skin fibroblast of yak (Bos grunniens) and cows of Bos indicus origin to hypoxia stress. Six primary fibroblast cell lines derived from three individuals each of Ladakhi yak (Bos grunniens) and Sahiwal cows (Bos indicus) were exposed to low oxygen concentration for a period of 24h, 48h and 72h. The expression of 10 important genes known to regulate hypoxia response such as HIF1A, VEGFA, EPAS1, ATP1A1, GLUT1, HMOX1, ECE1, TNF-A, GPx and SOD were evaluated in fibroblast cells of Ladakhi yak (LAY-Fb) and Sahiwal cows (SAC-Fb) during pre- and post-hypoxia stress. A panel of 10 reference genes (GAPDH, RPL4, EEF1A1, RPS9, HPRT1, UXT, RPS23, B2M, RPS15, ACTB) were also evaluated for their expression stability to perform accurate normalization. The expression of HIF1A was significantly (p < 0.05) induced in both LAY-Fb (2.29-fold) and SAC-Fb (2.07-fold) after 24h of hypoxia stress. The angiogenic (VEGFA), metabolic (GLUT1) and antioxidant genes (SOD and GPx) were also induced after 24h of hypoxia stress. However, EPAS1 and ATP1A1 induced significantly (p < 0.05) after 48h whereas, ECE1 expression induced significantly (p < 0.05) at 72h after exposure to hypoxia. The TNF-alpha which is a pro-inflammatory gene induced significantly (p < 0.05) at 24h in SAC-Fb and at 72h in LAY-Fb. The induction of hypoxia associated genes indicated the utility of skin derived fibroblast as cellular model to evaluate transcriptome signatures post hypoxia stress in populations adapted to diverse altitudes.

Effects of novel carbon sources additives on the solid-state sintering behavior and properties of SiC ceramics

To enhance the density of SiC and improve the purity of the SiC, carbon is frequently used as a sintering additive. SiC ceramics were prepared in this study by using various carbon sources (graphitic carbon microsphere, carbon black, and flake graphite) combined with B4C through spark plasma sintering (SPS) at temperatures ranging from 1800 °C to 1900 °C. Among the above carbon sources, the graphitic carbon microspheres were created by hydrothermal carbonization combined with catalytic graphitization. The influence of the carbon sources on the phase compositions, microstructure, physical properties, and oxidation resistance of the SiC specimens was investigated. The findings revealed that the SiC specimens prepared with graphitic carbon microsphere had a smaller crystallite size than those prepared with other kinds of carbon. The SiC specimens prepared with graphitic carbon microsphere displayed high relative density, hardness, fracture toughness, and remarkable oxidation resistance. This was attributed to the lower oxygen content, better dispersion, and higher chemical reactivity of graphitic carbon spheres. In terms of the oxidation resistance of SiC specimens, factors such as purity (residual carbon) and porosity were found to have a more significant impact than grain size. In general, the use of carbon sources with high reactivity and good dispersion is an effective method in preparing SiC ceramics.