Temperature Oxidation Research Articles

Superior oxidation resistance of a Y-Hf co-doped Al18Co30Cr10Fe10Ni32 eutectic high-entropy alloy at 1100–1300 °C

We report a study on the oxidation behavior of Al18Co30Cr10Fe10Ni32 eutectic high-entropy alloy co-doped with reactive elements (RE) Y and Hf at 1100–1300 °C. The highly stable eutectic microstructure of γ’/β phases within this alloy contributes to a low coefficient of thermal expansion, thus a low residual stress in the Al2O3 scale. The spinel with a low thickness is formed at the top of Al2O3 scale at 1100 °C due to the low Al diffusion coefficient of γ’-phase and low aspect ratio of β-phase in maze-like eutectic region. As the oxidation temperature increases, the oxidation products transition to exclusive Al2O3 at 1200 °C and 1300 °C, facilitated by the increased Al diffusion coefficient. The Al2O3 scale exhibits a dominated columnar grain microstructure at 1100–1300 °C, suggesting that the inward O diffusion plays more critical role than Al diffusion and thus leads to the low oxidation rate. Besides, the segregation of S to scale/metal interface is inhibited by the uniform RE distribution in the alloy resulting from the fine eutectic microstructure in the alloy. Overall, this alloy exhibits low residual stress in the oxide scale, slow oxidation rate, and the lack of interfacial sulfur segregation, thus contributing to its superior oxidation resistance. The strong oxidation resistance of Y-Hf co-doped Al18Co30Cr10Fe10Ni32 eutectic high-entropy alloy makes it a potential candidate for advanced oxidation-resistant alloy or coating applications.

Decoding the oxidation mechanism of Zircaloy-4 via in situ synchrotron X-ray diffraction and computational elucidation

Comprehensive understanding of the oxidation behavior of Zr alloys, a vital cladding material in nuclear power plants, is essential for developing improved materials and enhancing the safety and performance of nuclear systems. Herein, the bulk oxidation behavior in ambient air atmosphere of Zircaloy-4 were revisited through in situ synchrotron X-ray diffraction and DFT computation. The results reveal the phase transition sequences at a representative 900 °C oxidation temperature: hcp Zr recrystallizes rapidly and then transforms into bcc Zr while reaching the α+β transus, followed by speedy appearance of textured tetragonal (t-)ZrO2, monoclinic (m-)ZrO2 and ZrN that consume oxygen and nitrogen. Continuous air ingress favors t-ZrO2 and m-ZrO2 dominance, accompanied by re-oxidation of ZrN into t-ZrO2 due to its low thermodynamic stability revealed by experiment-informed DFT calculation and low oxygen activity at the oxide-metal interface. Ensemble-averaged lattice volume expansions during phase transitions have been quantified. This expansion-induced compressive stress promotes the presence of a significant fraction of t-ZrO2 at elevated temperature that eventually transforms into m-ZrO2 during cooling.

Design and evaluation of a low-cost sensor node for near-background methane measurement

Abstract. We developed a low-cost methane sensing node incorporating two metal oxide (MOx) sensors (Figaro Engineering TGS2611-E00 and TGS2600), humidity and temperature sensing, data storage, and telemetry. We deployed the prototype sensor alongside a reference methane analyzer at two sites: one outdoors and one indoors. We collected data at each site for several months across a range of environmental conditions (particularly temperature and humidity) and methane levels. We explored calibration models to investigate the performance of our system and its suitability for methane background monitoring and enhancement detection, first selecting a linear regression to fit a sensor baseline response and then fitting methane response by the sensor deviation from baseline. We achieved moderate accuracy in a 2 to 10 ppm methane range compared to data from the reference analyzer (RMSE < 0.6 ppm), but we found that the sensor response varied over time, possibly as a result of changes in non-targeted gas concentrations. We suggest that this cross sensitivity may be responsible for mixed results in previous studies. We discuss the implications of our results for the use of these and similar inexpensive MOx sensors for methane monitoring in the 2 to 10 ppm range.

A Concept of Online Refueling TRISO-Fueled and Salt-Cooled Reactor

This paper introduces a novel concept of a TRISO-fueled salt-cooled reactor (TFSCR). The core contains circulating pipes filled with molten salt carrying TRISO particles. The reactor achieves online refueling by slowly circulating the molten salt through the pipeline. The reactor utilizes the same molten salt as the coolant and graphite as the moderator. The reactor design has the characteristics of safety, economy, and nonproliferation. TRISO particles exhibit greater resistance to neutron irradiation, corrosion, oxidation, and high temperatures compared to conventional fuels. A molten salt-cooled reactor can also operate at higher temperatures, consequently enhancing power generation efficiency. Furthermore, lower operating pressures can mitigate the risk of significant damages and loss of coolant caused by accidents, thereby enhancing reactor safety. This paper presents the basic nuclear design of TFSCR under the assumptions concerning the average fuel power density, the volumetric core power density, and the core temperature. At the same time, the feasibility of online refueling and long-life operation was evaluated by fuel burnup calculation.

Analysis of temperature rise of low temperature adiabatic oxidation of sulfur-containing “coal-like substances”

ABSTRACT Spontaneous combustion of coal is one of the main natural disasters in the process of coal mining, and spontaneous combustion of sulfur-containing coal is an urgent problem to be solved. In order to understand the influence of different sulfur structures and sulfur content on spontaneous combustion tendency of coal, the self-developed synchronous temperature compensation adiabatic oxidation experiment system was used to study the oxidation self-heating performance of a series of sulfur-containing “coal-like materials.” Through the analysis of the heating rate of coal containing specific sulfur structure, it is considered that the time of adiabatic oxidation temperature of different organic sulfur “coal” to rise to 70°C is dimethyl sulfoxide > phenylene sulfide > dibenzothiophene. By analyzing the oxidation temperature rise characteristics of organic sulfur models with different sulfur contents, it is believed that the higher sulfur content, the faster the low temperature oxidation reaction of “coal-like substance,” the faster the temperature rise rate, and the shorter the time to reach the uncontrollable self-heating temperature, so the shorter the spontaneous combustion period. In general, in the stage of low temperature oxidation, active sulfur containing small molecules (dimethyl sulfoxide) promote the oxidation temperature rise, stable structure, larger molecular weight of dibenzothiophene slow down the “coal-like” oxidation temperature rise.

CO and O2 Interaction with Kinked Pt Surfaces.

We investigate the chemical interaction of carbon monoxide (CO) and oxygen (O2) with kink atoms on steps of platinum crystal surfaces using a specially designed Pt curved sample. We aim at describing the fundamental stages of the CO oxidation reaction, i.e., CO-covered/poisoned stage and O-covered/active stage, at the poorly known kinked Pt facets by probing CO uptake/saturation and O2 saturation, respectively. Based on the systematic analysis that the curved surface allows, and using high-resolution X-ray photoemission, a diversity of terrace and step/kink species are straightforwardly identified and accurately quantified, defining a smooth structural and chemical variation across different crystal planes. In the CO-saturated case, we observe a preferential adsorption at step edges, where the CO coverage reaches a CO molecule per step Pt atom, significantly higher than their close-packed analogous steps with straight terrace termination. For the O-saturated surface, a significantly higher O coverage is observed in kinked planes compared to the Pt(111) surface. While the strong adsorption of CO at the kinked edges points toward a higher ignition temperature of the CO oxidation at kinks as compared to terraces, the large O coverage at steps may lead to an increased reactivity of kinked surfaces during the active stage of the CO oxidation.

Combustion performance of aluminum modified boron nanoparticles coated with silane coupling agent

Boron (B) powder, with its high mass and volumetric heat values, makes it highly promising in the field of energetic materials. However, the oxide layer on the B surface is the most significant barrier to realizing its full potential as a fuel. How to eliminate or disrupt the oxide layer is currently an urgent problem that needs to be addressed. This study proposes an approach to enhance the combustion of nano-B powder by coating aluminum (Al) onto its surface using a silane coupling agent. The combustion characteristics of Al-modified B powder with different Al contents were investigated through experimental and molecular dynamic simulation methods, and the bidirectional diffusion mechanism on the interfacial layer of modified B particles was revealed. A small amount of Al powder can largely lower the initial oxidation temperature of B powder, increase the maximum flame temperature, and enhance the heat release. However, an excessive amount of Al powder leads to a deterioration in the combustion of B powder but can alter the combustion behavior and suppress the aggregation of B powder during the combustion. Additionally, combination reaction and redox reaction occurring during the combustion of B@Al samples not only reduce the burning time of B powder but also accelerate the flame expansion speed and improve the combustion efficiency. These results lay the foundation for the application of B@Al in the field of energetic materials.

TiO2 decorated MXene nanosheets for high-performance ammonia gas sensing at room-temperature

A room-temperature sensor with superior performance to detect traces of toxic gas molecules is highly desirable. MXenes, due to their unique planar structure, higher electrical conductivity and abundant functional groups on the surface, have emerged as leading low dimensional gas sensing materials. But, the gas sensors based on Ti3C2Tx MXene possess higher detection limit and poor long-term stability, thereby limiting their applications. However, TiO2 modified Ti3C2Tx as a gas sensing platform has displayed improved ammonia sensing performance. Here, we report a facile method to prepare Ti3C2Tx/TiO2 composite via calcination of Ti3C2Tx. The experimental results indicate that the oxidation temperature plays a key role in the morphology evolution and gas-sensing performance of Ti3C2/TiO2 composites. Compared to the as obtained Ti3C2Tx, the Ti3C2Tx/TiO2 composite obtained at 200 °C displays improved response to NH3 gas due to the formation of a heterointerface between Ti3C2Tx and TiO2. Room-temperature, selective ammonia detection down to 5 ppb has been obtained. Moreover, the device displayed a stable sensing response to 10 ppb of ammonia over the RH range of 26%–90%. It also displayed higher selectivity to NH3 over other analytes including dimethyl formamide, ethanol, isopropyl alcohol, methanol, acetone, chloroform, xylene and N-methyl pyrolidone. The results suggest that by appropriate engineering of the Ti3C2Tx/TiO2 composites, ammonia sensor with improved sensing performance can be designed.

Synthesis and characterization of Co3O4 spinel nanowall: understanding the growth mechanism and properties

Formation of spinel tricobalt tetraoxide (Co3O4) nanostructures through a controlled thermal oxidation process is discussed here. Thin films of high purity cobalt (Co) were deposited on glass/quartz substrates using an electron beam (E-beam) evaporation technique. Thermal oxidation of the as-deposited Co thin films was carried out at various oxidation temperatures (400 °C to 600 °C) for different durations (5 h to 15 h) to grow various oxide nanostructures. Different surface characterizations techniques were used to investigate the structure, chemistry and electronic properties of the as-grown cobalt oxide nanostructures. x-ray diffraction analysis revealed the presence of the CoO phase along with the Co3O4 phases at relatively lower oxidation temperature. However, the Co3O4 phase becomes more predominant for longer oxidation durations at higher oxidation temperatures. Field emission scanning electron microscopy analysis showed a surface morphological transition from nanowalls to nanograins with an increase in the oxidation temperature. The surface electrical conductivity of the oxidized Co films is also increased for higher oxidation temperature and/or duration mainly due to the oxide phase purity and larger particle sizes. Ultraviolet–visible spectroscopy indicated two distinct optical energy bandgaps, which effectively decreased with an increase in the oxidation temperature and duration. Raman spectroscopy identified five different Raman-active modes corresponding to the Co3O4 phase, with the F2g mode dominating at higher temperatures. All these findings provide clear insights into the structural, electrical, chemical and optical properties of cobalt oxide thin films. Moreover, it provides a mechanism on how to grow 2D nanowalls morphology of Co3O4 films which can further be used in energy, sensor or catalytic applications.

Structural control and mechanical properties optimization of porous SiC foams with three-dimensional network structure

In this paper, a new process for preparing porous SiC foam with three-dimensional network structure is presented. A certain thickness of SiC coating is deposited on the surface of ultra-light carbon skeleton by CVD process, so as to achieve effective control of its structure and mechanical properties. The effects of CVD deposition time on the density, porosity and skeleton thickness rates of SiC foams were explored. By increasing the CVD deposition time, the structure of SiC foams can be effectively regulated, and the mechanical properties of SiC foams can be significantly improved. The porosity of the prepared SiC foam can be adjusted in a wide range (26.9%∼94.68%). When the density of SiC foam increases from 0.67 g/cm3 to 2.36 g/cm3, its bending strength increases from 27.4 MPa to 136.9 MPa, which is significantly improved. After high temperature oxidation treatment (800–1200 °C), the mechanical properties of SiC foam will be further improved. However, when the oxidation temperature reaches 1400 °C, its mechanical properties will be reduced. This research provides a new idea for the preparation of high-performance porous SiC ceramics, and lays a foundation for its structural design, manufacture and application.

Scorodite synthesis process using solid iron oxides

The immobilization of arsenic in the form of scorodite (FeAsO4·2H2O), which has excellent chemical stability, is attracting attention as a method for treating wastewater containing high concentrations of arsenic generated at nonferrous metal smelting plants. Scorodite, with its low solubility and high arsenic content per volume, is expected to be an environmentally friendly arsenic fixation method suitable for final disposal. Various scorodite synthesis methods have been studied. The first synthesis method proposed is the hydrothermal method using an autoclave to synthesize highly crystalline scorodite. Although the hydrothermal method is capable of synthesizing scorodite with good crystallinity, from an economic point of view, scorodite synthesis under ambient pressure and at low temperatures is more attractive. As a low-temperature scorodite synthesis method under atmospheric pressure, the oxidation of Fe(II) process by O2 bubbling was proposed. In this method, ferrous sulfate is added to an arsenic-containing solution as a Fe ion source, and in situ oxidation of Fe(II) by O2 or air bubbling to form scorodite with good crystallinity. In addition to temperature, other conditions, pH, Fe/As ratio, and reaction time have been reported to affect scorodite crystallization. Recently, scorodite synthesis using solid iron oxide as the Fe source for scorodite synthesis, instead of aqueous Fe salt solutions, has attracted much attention. In this presentation, we will report on the investigation of reaction parameters, such as the type of iron oxide and reaction temperature, for the scorodite synthesis using solid iron oxide.

Study on High-Temperature, Ultra-Low Wear Behaviors of Ti6Al4V Alloy with Thermal Oxidation Treatment

Thermal oxidation (TO) is a simple and economical way to enhance the wear resistance of the Ti6Al4V alloy. The TO temperature has a very important effect on the tribological properties of the TiO2 layer formed. However, the impact of the oxidation temperature on the high-temperature tribological behavior of a TO-treated Ti6Al4V alloy is not clear. Therefore, the Ti6Al4V alloy was oxidized at 400 °C, 600 °C, and 700 °C for 36 h, and the sliding friction experiments were conducted at room temperature (RT) and 400 °C with a Si3N4 ball as the counter body to comparatively study the effect of the oxidation temperature on the high-temperature friction behavior of the TO-treated Ti6Al4V alloy. The results show that the TO treatment can effectively improve the wear resistance of the samples at both room and high temperatures. Among them, the oxidation-treated samples at 700 °C show the best wear resistance, with a reduction of 92.6% at high temperatures; the amount of wear loss at room temperature was so small that it was almost incalculable. At room temperature, the friction surface formed uneven agglomerate formations, resulting in an elevated coefficient of friction (CoF) compared to the untreated samples. At a high temperature, however, the CoF is reduced compared to the untreated samples due to the formation of a homogeneous transfer film in the wear area that is caused by the interaction of Si3N4 and oxygen.

Effect of oxidation temperature on physical properties of polycrystalline β-Ga2O3 grown by thermal oxidation of GaN in O2 ambient from 900 to 1400 °C

This study aimed to investigate the effect of oxidation temperature on the physical properties of β-Ga2O3 grown by thermal oxidation of GaN in the O2 ambient at high oxidation temperatures from 900 to 1400 °C. Notably, the analysis of the oxidation temperatures ranging from 1100 to 1400 °C remains unexplored in the other studies. The effects of the oxidation temperature on the physical properties were investigated via X-ray diffraction, X-ray photoelectron spectroscopy, and field-emission scanning electron microscopy (FESEM). At all oxidation temperatures, XPS results revealed oxygen deficiency. The top FESEM images indicated disordered nanocolumn structures on the surface of the oxide layer, which increased in abundance with oxidation temperatures exceeding 1100 °C. Energy-filtered high-resolution transmission electron microscopy images and the selected area electron diffraction patterns revealed that the top nanocolumns and the oxidized layer comprised polycrystalline β-Ga2O3. Additionally, the cross-sectional lamellae prepared through focused ion beam milling revealed an increase in the thickness of the β-Ga2O3 layer with oxidation temperature. To account for the variations in the oxide layer thickness, the oxidation temperatures were classified into two ranges of 900–1100 °C and 1100–1400 °C for calculating the activation energy. Moreover, this study assumed that the activation energy required for the oxidation process remained constant within each temperature interval. According to Arrhenius's model, the activation energy from 900 to 1100 °C was calculated to be 286.15 kJ/mol (2.97 eV). Furthermore, the activation energy from 1100 to 1400 °C was determined to be 111.33 kJ/mol (1.15 eV).

Dynamic evolution of terahertz permittivity of lignite during oxidation: Microstructural insights

Terahertz technology holds promise for monitoring coal fires and assessing associated risks, relying on the dielectric response of coal during the oxidation process. Besides, unraveling the response mechanism is crucial for enhancing the application's reliability. In light of these, this study focused on investigating the terahertz complex permittivity of lignite with different oxidation temperatures through microstructure analysis. Results indicated that oxidation temperature dependencies in the real and imaginary parts of lignite's permittivity, exhibiting a pattern of initial decrease followed by an increase. The decrease in permittivity during the dehydration and weight loss stage is primarily attributed to moisture content. In the oxygen absorption and weight gain stage, pore development and scattering effects contribute to the continuous decrease in real permittivity and rise in imaginary permittivity. During the oxidative decomposition stage, the hydroxyl group initiates an increased real permittivity. Upon reaching the combustion temperature, there is a sudden surge in permittivity, driven by the dominance of minerals in coal dielectric properties. The conclusions offer theoretical support for terahertz technology in monitoring coal fires, which can contribute to the sustainable development of the coal industry, mineral processing, and safety production.

Selective neodymium oxide recovery from permanent magnet scraps using waste pickling solutions

Neodymium (Nd) magnets are in high demand for use in the manufacture of electric vehicle motors and medical equipment such as magnetic resonance imaging. In this study, we describe a new process for recycling Nd permanent magnets (PMs). PM scrap powder was leached into a waste pickling solution, evaporated under reduced pressure, concentrated, and converted into an oxide via heat treatment. Nd was selectively leached from the prepared oxide using hydrochloric acid. Iron was removed from the leached solution, and the Nd composite was then recovered using a urea-mediated Nd-recovery method. The oxidation temperature was determined using a thermogravimetric analysis. High-purity Nd-oxide powders were obtained by calcination at 900 °C. This economical process enables the recovery of PM powder by relying on the pickling process and acid-regeneration plants, which are both essential in steel manufacturing.

Impact of fission product (Ce, Sn, Sr, Se) oxides on UO2 oxidation to U3O8

In order to investigate the impact of fission products on the oxidation of spent fuel in the cladding separation process, the oxidation behavior and kinetic mechanism of UO2 and impact of M (M = Ce, Sn, Sr, Se) oxides on the oxidation of UO2 to U3O8 were investigated by TG/DSC, XRD, FT-IR and Raman. It was found that the oxidation of UO2 to U3O8 went through two stages: UO2→U3O7; U3O7→U3O8. Doping M oxide in UO2 could not change the two-step mechanism, and significantly inhibited the formation of U3O8. The final products of CeO2 and SrO-doped UO2 oxidation contained 20% U3O7 and 47% U3O7, respectively. The doping of M oxide increased the onset oxidation temperature of the two oxidation stages of UO2 by 5–65 °C. In addition, the kinetic mechanism of UO2 oxidation was investigated and found that the first and second oxidation stages were controlled by 1st order reaction or nucleation and growth, and 2nd order reaction, respectively. The doping of M oxide significantly affected the kinetic mechanism of the first stage.

Study on the Inhibition Characteristics of Coal Spontaneous Combustion by Silica Gel Foam.

The spontaneous combustion of residual coal in abandoned mining areas severely affects the safe and efficient extraction of coal, employee occupational health, and regional environmental ecology. A technical measure for preventing and controlling the spontaneous combustion of residual coal involves injecting antispontaneous combustion materials into abandoned areas. In this study, the composition, preparation, and mechanism of action of silica gel foam, a material used to suppress spontaneous combustion during coal mining, were investigated to improve the performance of materials designed to prevent spontaneous combustion in abandoned areas. The inhibitory efficiency improved, and the mechanical strength and stability of the foam liquid film increased upon adding modified antioxidants and nanosilica particles to the gel foam. Macro performance tests, microstructural characterization, and chemical inhibition mechanism analyses verified the efficacy of silica gel foam for suppressing spontaneous combustion. The air leakage resistance of the silica gel foam effectively increased the air leakage resistance of the coal samples at different pressures. New radicals formed during the spontaneous combustion of coal comprising different inhibitors, as indicated by the g-factor results of electron paramagnetic resonance (EPR) spectroscopy analysis; the formation of radicals initially decreased and then increased when the inhibitor material changed. The concentration of free radicals decreased markedly during the spontaneous combustion process of both raw and inhibited coal samples at low oxidation temperatures (∼60-100 °C), indicating a marked inhibitory effect.

Green synthesis of nanosized Tantalum carbide (TaC) via natural polymer/tantalum oxide hybrid composites: A sustainable approach towards enhanced processing and properties

This study provides a green method for producing nanosized tantalum carbide (TaC) by pyrolyzing natural polymer (Gum karaya)/tantalum oxide hybrid composites, which is both sustainable and environmentally benign. The carbothermal reduction, carried out at 1500 °C, produces cubic TaC with a cell constant of ao=4.451 Å. The synthesised TaC reveals a near spherical morphology with an average size of 200 nm, far smaller than commercial TaC. The synthesised TaC displays a beginning oxidation temperature of 420 °C, as compared to the commercial powder (500 °C). Incorporating 5 wt% as-synthesized TaC to commercial TaC results in an impressive relative density of 98%, demonstrating the TaC ability as an excellent sintering aid. This green synthesis not only reduces the environmental impact of conventional methods, but also provides improved characteristics of nanosized TaC for advanced applications, contributing to the field of green nanotechnology by emphasizing safer production methods.

Effect of high temperature oxidation on mechanical and electromagnetic interference shielding effectiveness of Ti3SiC2 modified SiCf/BN/SiBCN composites

SiCf/BN/SiBCN composites were prepared through the technique of polymer infiltration pyrolysis (PIP). To enhance the electromagnetic interference (EMI) shielding effectiveness (SE), 20 wt% of Ti3SiC2 was incorporated into the composites. The study investigated the influence of different oxidation temperatures (1300 °C, 1400 °C, and 1500 °C) on both the mechanical properties and EMI SE of the composites. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were utilized to analyze the phase and microstructure of the composites, while characterizing their mechanical properties and EMI SE. The outcomes revealed a decline in the mechanical properties of the composites following high temperature oxidation, with the formation of SiO2 and TiO2 as the main oxidation products. Notably, an oxide layer formed on the material's surface at 1400 °C acted as a barrier to oxygen diffusion, facilitating self-healing of pores and cracks and thereby enhancing material protection. Moreover, the material oxidized at 1400 °C demonstrated a remarkable synergy between impedance matching and electromagnetic loss, resulting in the optimum EMI SE. The EMI SE of this material was 6.35% higher than the total shielding effectiveness at room temperature and effectively shielded 99.88% of electromagnetic waves.

Experimental and kinetic study of ammonia oxidation and NOx emissions at elevated pressures

To investigate the effects of pressure and equivalence ratio on ammonia oxidation and the emission of NOx, experiments were conducted in a flow reactor at atmospheric pressure and 5.0 MPa between 600 and 1250 K, with equivalence ratios ranging from 0.125 to 1.0. In addition, a kinetic model applicable to ammonia oxidation under high-pressure conditions was developed and validated against the performance of other recently published kinetic models with reference to several parameters associated with the ammonia oxidation and the emission of NOx under high-pressure conditions. The developed model was also validated against previously published experimental data collected under high-pressure conditions, and it can accurately capture the data obtained. The study found that the increase in pressure and oxygen content significantly enhanced the reactivity of NH3 and consequently resulted in increased NO and N2O concentrations at low temperatures. Based on a kinetic analysis using the developed model, the HO2 content was identified as the key factor influencing the difference in reactivity between atmospheric and high pressure. Sensitivity analysis revealed that H + O2 (+M) = HO2 (+M) inhibits NH3 consumption at atmospheric pressures but has a promoting effect at high pressures, because at high pressures the reaction generates a significant amount of HO2 radicals at low temperatures, increasing the reaction activity and reducing the onset temperature of ammonia oxidation. The H2NO system becomes even more critical under higher pressure, as more NH2 and O2 are converted to H2NO and NO. H2NO, NO, and N2O act as chain carriers in the reaction sequence, converting NH2 and O2 to OH and NO and accelerating the process of ammonia oxidation. At the same time, higher pressure enhances the NOx formation pathway due to the large amount of HO2 generated. However, as temperatures increase, O and OH radicals increase and DeNOx pathways dominate, resulting in lower NO and N2O contents. In the context of the equivalence ratios, the increase in the O2 content enhances the generation of HO2, leading to a greater tendency for NH2 to be converted in the NH2 + HO2 = HNO + H2O and NH2 + HO2 = H2NO + OH reaction pathways to HNO and H2NO, respectively. The HNO and H2NO produced are subsequently converted to NOx.