Oxidation Treatment Research Articles

Effect of ultrasonic pretreatment on physicochemical, thermal, and rheological properties of chemically modified corn starch

This study investigated the effects of ultrasonic and three chemical individual and dual modification treatments on corn starch's physicochemical, thermal, and rheological properties. Ultrasonication and the three chemical treatments disrupted the starch granules with a decrease in particle size and a significant increase in the ζ-potential. The hydrophilicity of ultrasonic-oxidized dual-modified starch (U-O-CS) was the highest, at 0.854 g/g. The lipophilicity of ultrasonic-esterified dual-modified starch (U-E-CS) was the highest, at 1.485 g/g. The gelatinization temperature of ultrasonic, oxidation, and cross-linking modified starches increased significantly, with cross-linking starches being the largest. Oxidative treatment significantly decreased the starch's G' and G" and weakened the textural properties. The rheological properties of U-O-CS were further weakened. The G' of the starch decreased after the esterification treatment, while the G" increased, and the textural properties were cut. The maximum rheological and textural properties were obtained for crosslinked modification, with a hardness value of 284.70 g.

Enhanced removal of antibiotic-resistant bacteria and resistance genes by three-dimensional electrochemical process using MgFe2O4-loaded biochar as both particle electrode and catalyst for peroxymonosulfate activation

In this study, MgFe2O4-loaded biochar (MFBC) was used as a three-dimensional particle electrode to active peroxymonosulfate (EC/MFBC/PMS) for the removal of antibiotic-resistant bacteria (ARB) and antibiotic resistance genes (ARGs). The results demonstrated that, under the conditions of 1.0 mM PMS concentration, 0.4 g/L material dosage, 5 V voltage intensity, and MFBC preparation temperature of 600 °C, the EC/MFBC600/PMS system achieved complete inactivation of E. coli DH5α within 5 min and the intracellular sul1 was reduced by 81.5 % after 30 min of the treatment. Compared to EC and PMS alone treatments, the conjugation transfer frequency of sul1 rapidly declined by 92.9 % within 2 min. The cell membrane, proteins, lipids, as well as intracellular and extracellular ARGs in E. coli DH5α were severely damaged by free radicals in solution and intracellular reactive oxygen species (ROS). Furthermore, up-regulation was observed in genes associated with oxidative stress, SOS response and cell membrane permeability in E. coli DH5α, however, no significant changes were observed in functional genes related to gene conjugation and transfer mechanisms. This study would contribute to the underlying of PMS activation by three-dimensional particle electrode, and provide novel insights into the mechanism of ARB inactivation and ARGs degradation under PMS advanced oxidation treatment.

Ultrahigh growth rate-induced thick 3C-SiC heteroepitaxial layers on 4H-SiC and its oxidation characteristics

The cubic 3C-SiC displays unique advantages in power electronics applications due to its high channel mobility and low SiO2/3C-SiC interface state density. Therefore, the epitaxial growth technology of 3C-SiC is one of the core technologies for preparing high-performance SiC power devices. In this work, we choose 4H-SiC as substrates to grow 3C-SiC with methyltrichlorosilane (MTS)-H2 complex precursor and acheieved an ultrahigh epitaxial growth rate up to 278 μm/h. Then the oxidation treatment has been conducted. The elemental composition, surface morphology, and crystalline phase of the prepared 3C-SiC/4H–SiC thick films were comprehensively characterized with SEM, Raman, XRD and TEM techniques. The growth mechanism and oxidation characteristics of the 3C-SiC/4H-SiC heteroepitaxial layers were analyzed based on experimental phenomena.

Assessing the impact of temperature, pH, light and chemical oxidation on fucoxanthin colour changes, antioxidant activity and the resulting metabolites.

The present study evaluated the effects of temperature, pH, light and chemical oxidation on fucoxanthin changes in terms of colour, antioxidant activity and metabolomic profile. Additionally, the correlation between antioxidant activity and identified metabolites was analysed. It was found that colour change was significantly reduced at elevated heat (100 °C, *∆E = 0.81 ± 0.05), reduced pH (pH 3, *∆E = 0.59 ± 0.04) and length of light exposure (*∆E = 3.16 ± 0.04). Antioxidant activity decreased under all treatments. Among the temperatures tested, fucoxanthin exhibited the highest activity at 60 °C, ranging from 0.92 to 3.04 mg Trolox equivalents (TE) g-1. Significant activity reductions (P < 0.05) were observed as a result of pH changes in the 2,2-diphenyl-1-picrylhydrazyl and β-carotene bleaching assays. Exposure to light 2: warm white lamp for 120 h significantly reduced antioxidant activity (0.01 to 1.70 mg TE g-1). Chemical oxidation also led to reduced activity, ranging from 0.18 to 0.29 mg TE g-1. Multivariate data analysis revealed distinct profiles for temperature, pH, light and chemical oxidation treatments. Liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based metabolomics analysis identified 10 metabolites, and significant correlations (P < 0.05) indicate that these metabolites contributed to the samples' antioxidant activities. In conclusion, fucoxanthin tolerates well at 60 °C, within pH range 3-9, and within 8 h of light exposure, as indicated by its consistent antioxidant activity and minimal colour change. Each treatment resulted in distinct metabolite concentrations, as shown by LC-MS/MS-based metabolomics analysis. Further research into these metabolites could advance the understanding of their roles and aid in optimising processing conditions to favour beneficial metabolites. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Evolution of high temperature oxidation properties of SiCf/SiCN composites with BN interphase

In this study, SiC/SiCN composites with BN interphase were prepared using chemical vapor infiltration (CVI) and polymer infiltration and pyrolysis (PIP) methods. The evolution and related mechanisms of mechanical and microwave absorption properties of the composites after oxidation at 800 °C, 1000 °C, 1200 °C, and 1400 °C were investigated. The results showed that with the elevating of oxidation temperature, the flexural strength of SiC/SiCN composites gradually decreased, with a retention rate of 56.7 % after oxidation at 1400 °C. The main reasons for the deterioration of mechanical properties were the changes in the crystal structure of SiC fibers under high-temperature conditions and the formation of brittle SiO2 phases on the surface and interior of the SiCN matrix. With the increase in oxidation temperature, the microwave absorption performance of the composites showed an enhancing trend. The main reasons were that after oxidation treatment, the reduction of free carbon content and the formation of SiO2 film layers from the oxidation of SiC and SiCN led to a decrease in the complex permittivity of the composites, resulting in better impedance matching and dielectric loss capabilities. The contributions of BN interphase to stress dispersion, interface polarization, and oxidation protection significantly enhance the mechanical and electromagnetic absorption properties of the composites. Therefore, SiC/SiCN composites are high-temperature structural microwave absorbing materials with great application prospects.

Unravelling the antioxidant behaviour of self-assembly β-Sheet in silk fibroin

Local oxidative stress in diseases or injury severely hinders cell homeostasis and organ regeneration. Antioxidant therapy is an effective strategy for oxidative stress treatment. Biomaterials with good biocompatibility and reactive oxygen species (ROS) scavenging ability are good choices for antioxidant therapeutics. However, there are few natural biomaterials that are identified with both biocompatibility and strong antioxidant activity. Here, we show, for the first time, that silk fibroin (SF) is a strong antioxidant, which can eliminate ROS in both cells and zebrafish. We further demonstrate that the β-sheet structures turn into a random coiled structure when SF is treated with hydrogen peroxide. The content of β-sheet structures can be increased by heating, thus enhancing the antioxidation properties of SF. Therefore, SF can serve as a good antioxidant biomaterial for therapeutics, and its β-sheet structure-based antioxidation mechanism provides a novel theoretical basis, which could be a new cue for more antioxidant biomaterial discovery and identification.

Growth of α-Al2O3 layer involving abnormal oxides in FeCrAl alloy tube fabricated by WEDM process and electrical insulating performance in fusion reactor blanket

The tubular specimens of FeCrAl alloy APMT (Fe-22Cr-5Al-3Mo) were fabricated by a wire electrical discharge machining (WEDM) process. The oxidation characteristics of the machined surface were investigated by means of the oxidation tests performed in air atmosphere at the temperatures of 1273 K and 1373 K up to 100 h. The abnormal oxides such as CuAl2O4 and ZnAl2O4 were grew on the recast layer which was locally remained on the machined surface even after the mechanical polishing procedure. The α-Al2O3 layer involving the abnormal oxides was formed on the machined surface in the oxidation treatment at 1273 K for 10 h. The apparent electrical conductivity of the layer involving the abnormal oxides was larger than that without the abnormal oxides. Thick Al-rich oxide layer was formed under the abnormal oxides when the oxidation treatment was performed at 1373 K. The apparent electrical conductivity of the oxide layer became lower due to the presence of the thick Al-rich oxide. This oxide layer formed at 1373 K could function as an electrical insulating layer to reduce the magnetohydrodynamic pressure drop in liquid breeder blanket systems of magnetic confinement fusion reactors.

The influence of anodization on laser transmission welding between high borosilicate glass and TC4 titanium alloy

This study investigates the influence of the thickness of the oxide film formed on the surface of TC4 titanium alloy after anodization on the laser transmission welding between the titanium alloy and high borosilicate glass. The effects of oxidation time on the morphology and thickness of the oxide film were examined, and the elemental and phase composition of the oxide film were characterized. The differences in welding strength, weld morphology, and fracture surface between the titanium alloy before and after oxidation treatment and high borosilicate glass welding were compared, and analyzed the welding seam formation mechanism. Within our research scope, the results indicate that with an increase in oxide film thickness, the surface roughness gradually increases and the internal voids gradually increase, resulting in a decrease trend in the bonding strength of the welded joints with the increase in oxide film thickness. The interpenetrating structure formed by the mutual infiltration of glass and metal in the molten pool is identified as the main reason for their connection.

Porous BINAP-based polyaromatic polymers for the continuous base-free Ru-catalysed decomposition of aqueous formic acid

In this work, a Suzuki cross-coupling procedure towards highly porous BINAP-based polymeric Ru-catalyst materials with tunable specific surface areas (SSAs) were synthesized and their stability towards reducing conditions was investigated. After the removal of Pd impurities by an oxidative treatment with H2O2/HCl, P=O reduction and metal loading, the resulting catalysts were employed for the base-free ruthenium-catalyzed decomposition of aqueous formic acid to CO2 and H2 with TOFs of up to 134000 h−1 and TONs up to 920000.

Surface chlorination of IrO2(110) by HCl.

The ability to controllably chlorinate metal-oxide surfaces can provide opportunities for designing selective oxidation catalysts. In the present study, we investigated the surface chlorination of IrO2(110) by HCl using temperature programmed reaction spectroscopy (TPRS), x-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations. We find that exposing IrO2(110) to HCl, followed by heating to 650K in ultrahigh vacuum, produces nearly equal quantities of on-top and bridging Cl atoms on the surface, Clt and Clbr, where the Clbr atoms replace O-atoms that are removed from the surface by H2O formation. After HCl adsorption at 85K, only H2O desorbs at low Cl coverages during TPRS, but HCl begins to desorb in increasing yields as the Cl coverage is increased above about 0.5 monolayer (ML). The desorption of Cl2 was not observed under any conditions, in good agreement with the high barrier for this reaction predicted by DFT. A maximum Cl coverage of 1 ML, with nearly equal coverages of Clt and Clbr atoms, could be generated by reacting HCl with IrO2(110) in UHV. Our results suggest that a kinetic competition between recombinative HCl and H2O desorption under the conditions studied limits the saturation Cl coverage to a value less than the 2 ML maximum predicted by thermodynamics. XPS further shows that the partitioning of Cl between the Clt and Clbr states can be altered by subjecting partially chlorinated IrO2(110) to reductive or oxidative treatments, demonstrating that the Cl site population can change dynamically in response to the gas environment. Our results provide insights for understanding the chlorination of IrO2(110) by HCl and can enable future experimental studies to determine how Cl-modification alters the surface chemical reactivity of IrO2(110) and potentially enhances selectivity toward partial oxidation chemistry.

Theoretical investigation on the influence of H2 ${{\rm{H}}}_{2}$ additions on the He + 1% O2 ${{\rm{O}}}_{2}$ plasma reactivity for water treatment applications

AbstractPlasma‐based technologies offer environmentally friendly means of effective water purification. Here, we present a discharge system with He + 1% . Tunable amounts of were introduced to control the yield of reactive species. Detailed exploration of the system provides a deeper understanding of some of the fundamental chemical kinetics related to plasma‐based wastewater treatment. A global model was used to investigate the effect of additions on the yield of some important reactive species for advanced oxidation treatment of wastewater. Humidity leakage was considered to simulate the effect of humidified environments. The pathway analysis module provides deeper insight into chemical kinetics. It was concluded that additives can be used in tailoring plasma yield for water treatment applications.

Oxidative regulation and cytoprotective effects of γ-polyglutamic acid on surimi sol subjected to freeze-thaw process

Frozen surimi sol incline to protein oxidation, but the quality control strategies based on oxidation remain limited. Hence, the antioxidant and cryoprotective effects of γ-polyglutamic acid (γ-PGA) on freeze-thawed salt-dissolved myofibrillar protein (MP) sol were investigated. Results showed that γ-PGA could effectively regulate protein oxidation of MP sol during freeze-thawing with lower carbonyl contents and less oxidative cross-linking. Meanwhile, γ-PGA primely maintained sol protein structures, showing reduction of 15.28% of salt soluble protein contents at γ-PGA addition of 0.04% under unoxidized condition. Additionally, compared to the control group without oxidation treatment, cooking loss of heat-induced gel with 0.04% γ-PGA decreased by 47.19%, while gel strength obviously increased by 57.22% respectively. Overall, moderate γ-PGA addition (0.04%) could inhibit protein oxidation of sol, further improving frozen stability of sol through hydrogen bonds and hydrophobic interaction, but excessive γ-PGA was adverse to sol quality due to severe cross-linking between γ-PGA and MP.

Mechanism-guided strategies for combating antibiotic resistance.

Bacterial antibiotic resistance has been recognized as a global threat to public health. It challenges the antibiotics currently used in clinical practice and causes severe and often fatal infectious diseases. Fighting against antibiotic-resistant bacteria (ARB) is growing more urgent. While understanding the molecular mechanisms that underlie resistance is a prerequisite, several major mechanisms have been previously proposed including bacterial efflux systems, reduced cell membrane permeability, antibiotic inactivation by enzymes, target modification, and target protection. In this context, this review presents a panel of promising and potential strategies to combat antibiotic resistance/resistant bacteria. Different types of direct-acting and indirect resistance breakers, such as efflux pump inhibitors, antibiotic adjuvants, and oxidative treatments are discussed. In addition, the emerging multi-omics approaches for rapid resistance identification and promising alternatives to existing antibiotics are highlighted. Overall, this review suggests that continued effort and investment in research are required to develop new antibiotics and alternatives to existing antibiotics and translate them into environmental and clinical applications.

Degradation pathways and product formation mechanisms of asphaltene in supercritical water

Asphaltene is the compound with the most complex structure and the most difficult degradation in oily sludge, which is the key to limit the efficiency of supercritical water oxidation treatment of oily sludge. In this paper, the supercritical water oxidation process of asphaltene was investigated in terms of free radical reaction, degradation pathway, and product generation mechanism using ReaxFF molecular dynamics simulation method. The results showed that increasing temperature, increasing O2, and increasing H2O have different effects on HO2·generation. Benzene rings undergo fusion and condensation through hydrogenation abstraction and oxygen addition reactions, subsequently breaking down into long-chain alkanes. Increasing O2 can effectively promote the ring-opening of nitrogen-containing heterocycles. -COOH is the most important intermediate fragment for CO and CO2 generation, and there is a reaction competition with -CHO3 and -CO3. When the number of oxygen molecules increases from 300 to 700, the reaction frequency of -CHO3 and -CO3 to generate CO and CO2 increases by 17.14 % and 12.77 %·H2O determines the production of H2 by controlling the number of H·radicals present. As the amount of H2O increases from 500 to 1500, the product ratio of H2 increases from 12.73 % to 21.31 %. Environmental implicationAsphaltene is the most structurally complex organic matter in oily sludge, and its presence makes it difficult for oily sludge to be completely degraded by conventional treatment methods such as pyrolysis and incineration. Polycyclic aromatic hydrocarbons (PAHs) represented by asphaltene increase the carcinogenicity and mutagenicity of oily sludge, and even irreversibly pollute soil and groundwater. Supercritical water oxidation, as an efficient organic waste treatment technology, can realize harmlessness in a green and efficient way. So the study on the mechanism of supercritical water oxidation of asphaltene is of great significance for environmental protection.

Comparing Electrode Overpotential Contributions in Vrfbs Amongst Multiple Techniques

Redox flow batteries (RFBs) offer a potential remedy for the escalating need for energy storage amid the ongoing transition from carbon-intensive fossil energy to renewable energy sources. Yet, many RFB chemistries are shown to have low energy efficiencies which can be attributed, in part, to ineffective electrode materials. Identifying overpotential contributions from electrodes under operating conditions is a key step in understanding how to design better RFB electrodes Previously, three-electrode setups using rotating disk electrodes (RDE) were the effective technique at isolating overpotentials; however, this can only be accomplished by looking at one side of the RFB at a time. RDEs do not easily replicate the operational conditions of a power cell or the porous nature of carbon electrodes used in RFBs. Alongside the normal operation of an RFB, symmetry cells are another approach that can be utilized in quantifying the performance of electrodes. The advantage of a symmetrical cell setup allows us to monitor the overpotential contributions of two different electrodes in the same electrolyte concurrently. Membrane-based reference electrodes (MBRE), and other reference electrode integration concepts, allow us to use three-electrode techniques in operational RFB power cells. As a case study, we examined the effect of oxidative electrode treatments on the positive and negative side of the VRFB using multiple methods. While other studies have shown that an untreated negative electrode may be the key inhibitor in VRFB performance, we have quantified the overpotential at 50% state of charge to be 194 mV when 50 mA cm-2 is applied. After an oxidative treatment is applied to the negative electrode, the overpotential is reduced to 111 mV. Applying this to other techniques, we can compare the effectiveness of a non-symmetry cell setup vs. a symmetry cell setup, which displayed that oxidative treatment techniques appear to have an opposite effect on the positive electrode. A treated-positive electrode shows an overpotential of around 100 mV whereas an untreated-positive electrode only contributes 15 mV less of overpotential. These findings are further compared using common reference electrodes placed in the electrolyte tank, providing insights into the effectiveness of power cell techniques in improving RFB electrode performance.

O-Targeted Carbon Hybrid Orbital Conversion to Produce sp2-Rich Closed Pores for Sodium-Storage Hard Carbon.

Biomass-based hard carbon has the advantages of a balanced cost and electrochemical performance, making it the most promising anode material for sodium-ion batteries. However, due to the structural limitations of biomass (such as macropores and impurities), it still faces the problems of low specific capacity and initial Coulombic efficiency (ICE). Herein, an integrated strategy of biomass liquefaction and oxidation treatment is proposed to fabricate hard carbon with low ash content and sp2-rich closed pores. Specifically, liquefaction treatment can break through the inherent constraints of biomass, while oxidation treatment with O-targeted effect can directionally convert C─C/C─O bonds into C═O/O═C─O bonds, which would promote the formation of closed pores and the rearrangement into sp2-carbon within the graphene layer. Moreover, it is well demonstrated that the hard carbon interface rich in sp2 hybridization can induce the generation of an inorganic-rich solid electrolyte interface, contributing to fast ion migration and excellent interfacial stability. As a result, the optimized hard carbon with maximum closed pore volume and sp2/sp3 ratio can exhibit a high capacity of 347.3mAhg-1 at 20mAg-1 with the ICE of 90.5%, and a capacity of 110.4mAhg-1 at 5.0Ag-1 after 10000 cycles.

Binding between Cu2+/Zn2+ and aged polyethylene and polyethylene terephthalate microplastics in swine wastewaters: Adsorption behavior, and mechanism insights

Microplastics (MPs) have aroused growing environmental concerns due to their biotoxicity and vital roles in accelerating the spread of toxic elements. Illuminating the interactions between MPs and heavy metals (HMs) is crucial for understanding the transport and fate of HM-loaded MPs in specific environmentally relevant scenarios. Herein, the adsorption of copper (Cu2+) and zinc (Zn2+) ions over polyethylene (PE) and polyethylene terephthalate (PET) particulates before and after heat persulfate oxidation (HPO) treatment was comprehensively evaluated in simulated and real swine wastewaters. The effects of intrinsic properties (i.e., degree of weathering, size, type) of MPs and environmental factors (i.e., pH, ionic strength, and co-occurring species) on adsorption were investigated thoroughly. It was observed that HPO treatment expedites the fragmentation of pristine MPs, and renders MPs with a variety of oxygen-rich functional groups, which are likely to act as new active sites for binding both HMs. The adsorption of both HMs is pH- and ionic strength-dependent at a pH of 4–6. Co-occurring species such as humic acid (HA) and tetracycline (TC) appear to enhance the affinity of both aged MPs for Cu2+ and Zn2+ ions via bridging complexation. However, co-occurring nutrient species (e.g., phosphate and ammonia) demonstrate different impacts on the adsorption, improving uptake of Cu2+ by precipitation while lowering affinity for Zn2+ owing to the formation of soluble zinc-ammonia complex. Spectroscopic analysis indicates that the dominant adsorption mechanism mainly involves electrostatic interactions and surface complexation. These findings provided fundamental insights into the interactions between aged MPs and HMs in swine wastewaters and might be extended to other nutrient-rich wastewaters.

Synergy of oxygen reduction for H2O2 production and electro-fenton induced by atomic hydrogen over a bifunctional cathode towards water purification

In the Electro-Fenton (EF) process, hydrogen peroxide (H2O2) is produced in situ by a two-electron oxygen reduction reaction (2e ORR), which is further activated by electrocatalysts to generate reactive oxygen specieces (ROS). However, the selectivity of 2e transfer from catalysts to O2 is still unsatisfactory, resulting in the insufficient H2O2 availability. Carbon based materials with abundant oxygen-containing functional groups have been used as excellent 2e ORR electrocatalysts, and atomic hydrogen (H*) can quickly transfer one electron to H2O2 in a wide pH range and avoiding the restrict of traditional Fenton reaction. Herein, nickel nanoparticles growth on oxidized carbon deposited on modified carbon felt (Ni/Co@CFAO) was prepared as a bifunctional catalytic electrode coupling 2e ORR to form H2O2 with H* reducing H2O2 to produce ROS for highly efficient degradation of antibiotics. Electrochemical oxidation and thermal treatment were used to modulate the structure of carbon substrates for increasing the electro-generation of H2O2, while H* was produced over Ni sites through H2O/H+ reduction constructing an in-situ EF system. The experimental results indicated that 2e ORR and H* induced EF processes could promote each other mutually. The optimized Ni/Co@CFAO with a Ni:C mass ratio of 1:9 exhibited a high 2e selectivity and H2O2 yield of 49 mg L−1. As a result, the designed Ni/Co@CFAO exhibited excellent electrocatalytic ability to degrade tetracycline (TC) under different aqueous environmental conditions, and achieved 98.5% TC removal efficiency within 60 min H2O2 and H* were generated simultaneously at the bifunctional cathode and react to form strong oxidizing free radicals •OH. At the same time, O2 gained an electron to form •O2−, which could react with •OH and H2O to form 1O2, which had relatively long life (10−6∼10−3 s), further promoting the efficient removal of antibiotics in water.

Regulating the active hydroxyl group of starch: Revealing the evolution of hard carbon structure and sodium storage behavior

The active hydroxyl group of starch has a crucial effect in regulating the microstructure of hard carbon anodes for sodium-ion batteries. By optimizing the chemical structure of starch and controlling the pyrolysis process, high-performance hard carbon materials can be obtained. These active hydroxyl groups are primarily located on the terminal and ring structures of glucose units, exerting significant influence on the formation and performance of hard carbon. Our results demonstrate that low-temperature oxidation treatment effectively modifies the terminal hydroxyl groups in precursor materials, facilitating chain cross-linking and leading to a more robust hard carbon structure. This cross-linking effect helps suppress excessive foaming during pyrolysis, thereby enhancing the stability of the hard carbon structure. Furthermore, by modifying the hydroxyl group on the ring structure of precursors, we can control the pyrolysis process, promote pore closure, and further improve the low plateau capacity of hard carbon anode materials from 153.95 to 219.58 mAh g −1. This study offers novel insights into harnessing and understanding starch's active hydroxyl groups in preparing hard carbon materials—a significant contribution towards optimizing their performance as anode materials.

Remarkable enhancement of the corrosive-wear resistance for Ti-Zr-Hf-Nb-Fe high-entropy alloys by a facile high-temperature oxidation treatment

The surface performances of TiZrHfNbFe refractory high-entropy alloys (RHEAs) were improved by a facile oxidation treatment at 1000 °C. Results indicated that the anomalous retarded oxidation behavior of the RHEA enabled the formation of a dense and robust oxide layer, demonstrating superior wear and corrosion resistance. The oxidation resistance of the RHEA was related to the development of Ti2ZrO6 on the surface and acicular HfO2 in the inner oxide layer. Additionally, the oxidation mechanism of the RHEA was elucidated, based on principles of oxidation thermodynamics and kinetics, providing foundations for applications as implant materials.