High-temperature Treatment Research Articles

Improvement of charge trapping memory performance by modulating band alignment with oxygen plasma

Metal-oxide charge trapping memory (CTM) integration into amorphous and organic flexible devices encounters challenges due to high-temperature treatment. Our approach enhances memory performance via room-temperature oxygen plasma treatment, subtly adjusting surface band alignment without changing the original material structure and surface roughness. Infiltration of oxygen plasma induces band alignment bending, creating a barrier for charge trapping. The device with oxygen plasma treatment exhibits an impressive 19.06 V memory window and a charge trapping density of 3.58 × 1013/cm2. In comparison, the memory window of untreated device only has 5.56 V, demonstrating that oxygen plasma treatment significantly improves memory characteristics. The charge retention rate exhibits outstanding stability, potentially reaching 94% after a decade. It should be noted that careful control during plasma treatment is crucial to maintaining optimal memory effects. This facile, efficient technique, applicable to various oxide layers, offers a way for future advancements in metal-oxide CTM technology.

Precise Construction of the Triple-Phase Boundary and Its Antiphosphate Poisoning Effect in the Confined Region.

As a critical component for the oxygen reduction reaction (ORR), platinum (Pt) catalysts exhibit promising catalytic performance in High-temperature-proton exchange membrane fuel cells (HT-PEMFCs). Despite their success, HT-PEMFCs primarily utilize phosphoric acid-doped polybenzimidazole (PA-PBI) as the proton exchange membrane, and the phosphoric acid within the PBI matrix tends to leach onto the Pt-based layers, easily causing toxicity. Herein, we first propose UiO-66@Pt3Co1-T composites with precisely engineered interfacial structures. The UiO-66@Pt3Co1-T exhibits an octahedral porous framework with uniform structural dimensions and even distribution of surface nanoparticles, which demonstrate superior ORR performance compared to commercial Pt/C. The unique structure and morphology of the composites also exhibit a favorable half-wave potential in different concentrations of phosphoric acid electrolyte, regulated by the phosphoric acid adsorption site and intensity.This finding suggests that the incorporation of Co could effectively modulate the Pt d-band center, thereby enhancing the ORR performance. Furthermore, the selective adsorption of phosphoric acid by ZrO2 enables precise control over the phosphoric acid distribution. Notably, the retention of the octahedral framework post high-temperature treatment facilitates the establishment of dual transport pathways for gases and protons, leading to a stable and efficient triple-phase boundary.

Immunity Induction in Catfish (Clarias gariepinus) with Feed Containing Red Ginger Extract after High Temperature Treatment

This study aims to evaluate the effect of feeding feed containing red ginger extract on the immunity and survival of catfish (Clarias gariepinus) fingerlings exposed to high temperature conditions. The research was carried out experimentally with a Completely Randomized Design (CRD) consisting of four treatment doses of red ginger extract (A: 0 ml/kg, B: 30 ml/kg, C: 40 ml/kg, D: 50 ml/kg) and three replications. Parameters observed included survival rate, white blood cell count, red blood cell count. The results showed that the addition of red ginger extract to feed was able to increase catfish survival by up to 90% at a dose of 50 ml/kg. A significant increase in the number of white blood cells and red blood cells in fish given red ginger extract indicates a better immune response. Red ginger extract has proven effective in helping fish adapt to thermal stress by increasing immunity and resistance to high water temperatures.

Characterization of the thermomechanical and aging behaviour of PAEK and CF/PAEK composites under long-term high-temperatures

The growing use of poly(aryl ether ketone) (PAEK) polymers reinforced with carbon fiber (CF) aims to meet the increasing demand for thermoplastic composites in applications that require excellent mechanical properties and thermal stability at higher temperatures. This study investigated the physicochemical properties of PAEK and CF/PAEK composites under long-term high-temperature exposure (150 °C, 200 °C and 250 °C) for durations of 15, 30, and 45 days, aiming to elucidate the durability mechanisms and enhance understanding of their performance. Specifically, the changes in the flexural properties and dynamic thermo-mechanical properties of the materials were evaluated after long-term high-temperature treatment. The results indicated that both PAEK and CF/PAEK composites possess substantial potential for long-term high-temperature applications, with CF not significantly altering the fundamental high-temperature response of the PAEK matrix. Regarding durability mechanisms, at 150 °C, PAEK's amorphous region undergoes chain reorientation, while temperatures of 200 °C and 250 °C induce significant secondary crystallization, which significantly improved the high-temperature mechanical properties of these materials. Additionally, at temperatures up to 250 °C, shorter linear chain fragments form through oxidative scission in PAEK's amorphous molecular chains. This work not only enriches the existing data on the properties of PAEK and CF/PAEK composites after long-term high-temperature treatment, but also provides further insights into their durability mechanisms.

Effects of mineral fertilization (NPK) on combined high temperature and ozone damage in rice

BackgroundIncreasing concern has recently been highlighted regarding crop damage due to extreme weather events caused by global warming and the increased production of ground-level ozone. Several studies have investigated rice growth in response to fertilization conditions under various environmental stress conditions; however, studies on growth development in response to fertilization conditions under combined high-temperature/ozone treatment conditions are scarce. In this study, we aimed investigate the growth and physiological development of rice under combined high temperature and ozone treatment conditions and to reveal the damage-mitigation effects of NPK fertilization treatments.ResultsThe plants were treated with varying levels of NPK [N2 (N-P-K: 9.0-4.5-4.0 kg/a), P2 (4.5-9.0-4.0 kg/a), K2 (4.5-4.5-8.0 kg/a), and control (4.5-4.5-4.0 kg/10a).] under combined high-temperature (35 ℃) and ozone (150 pb) treatment conditions. Analysis of the growth metrics, including plant height, leaf age, dry weight, and the plant height/leaf age (PH/L) ratio were revealed that combined high-temperature/ozone treatment promoted the phenological development indicated by increasing leaf age but decreased the plant height and dry weight indicating its negative effect on quantitative growth. The effects of this combined high-temperature/ozone treatment on growth were alleviated by NPK fertilization, particularly in K2 treatment but worsened in N2 treatment. Visible damage symptoms in rice leaves induced by exposure to the combined stressors was also alleviated by the K2 treatment. At the physiological level, K2 treatment reduced the expression of OsF3H2, which is associated with antioxidant activity, suggesting that potassium improved stress tolerance. Additionally, expression of genes related to abscisic acid (ABA) metabolism showed increased OsNECD (ABA synthesis) and decreased OsCYP707A3 (ABA degradation) in the K2 treatment, promoting a stronger adaptive stress response. Stomatal conductance measurements indicated a slight increase under K2 treatment, reflecting enhanced regulation of stomatal function during stress.ConclusionThe study highlights the potential of potassium fertilization to mitigate combined high-temperature and ozone stress in rice, suggesting it as a strategy to improve crop resilience and optimize fertilization. The findings offer insights into fertilization treatments and can guide future research on stress tolerance in crops.

Analysis of Differential Alternative Splicing in Largemouth Bass After High Temperature Exposure.

Temperature is one of the critical factors affecting the physiological functions of fish. With ongoing global warming, changes in water temperature have a profound impact on fish species. Alternative splicing, being a significant mechanism for gene expression regulation, facilitates fish to adapt and thrive in dynamic and varied aquatic environments. Our study used transcriptome sequencing to analyze alternative splicing in largemouth bass gills at 34 °C for 24 h. The findings indicated an increase in both alternative splicing events and alternative splicing genes after high temperature treatment. Specifically, the comparative analysis revealed a total of 674 differential alternative splicing events and 517 differential alternative splicing genes. Enrichment analysis of differential alternative splicing genes revealed significant associations with various gene ontology (GO) terms and KEGG pathways, particularly in immune-related pathways like necroptosis, apoptosis, and the C-type lectin receptor signaling pathway. These results emphasize that some RNA splicing-related genes are involved in the response of largemouth bass to high temperatures.

Dissolution of Primary Carbides and Formation and Healing of Kirkendall Voids in Bearing Steel under Pulsed Electric Current

The alloying elements in 8Cr4Mo4V bearing steel tend to form large primary carbides with carbon, which not only causes element segregation but also becomes the primary source of fatigue crack initiation, thereby decreasing the material's usability and machinability. Owing to the excellent thermal stability of primary carbides, traditional homogenization annealing requires high temperatures, which is both time‐ and energy‐intensive. Excessively high heat treatment temperatures can also result in “overburning” of the sample. Herein, primary carbides are rapidly dissolved at low temperatures using pulsed electric current treatment. The additional free energy introduced by the pulsed electric current lowers the thermodynamic barrier for carbide dissolution. During the second‐phase dissolution process, the unbalanced diffusion of elements may cause the formation of Kirkendall voids. Due to the difference in electrical conductivity between the voids and the matrix, the pulsed electric current generates thermal compressive stress on the voids, promoting rapid atom migration to these voids and accelerating their healing. This pulse‐current treatment technology offers a novel method for the rapid dissolution of carbides in alloys at low temperatures and for the rapid healing of related voids.

Sulfur doped hollow cobalt–nitrogen–carbon oxidase-mimicking nanozyme enable sensitive chemiluminescence sensing serum total antioxidant capacity

Heteroatom doping is one of most important methodology for heightening catalytic activity of a nanozyme through modulating electronic configuration and coordinated environment of metal atoms. Here, a nitrogen/sulfur co-doped cobalt-decorated hollow carbon structure (CoS/NC) was fabricated through a simple and manageable template-assisted synthetic strategy, following high-temperature carbonization treatment. Remarkably, the CoS/NC has superior oxidase-mimicking activity than its counterparts and displays excellent catalytic action on the chemiluminescence (CL) reaction between luminol and dissolved oxygen (O2). The CoS/NC nanozyme-based CL system is highly sensitive to physiologically relevant antioxidants of both species including single electron transfer and hydrogen atom transfer. The detection limits can be reached as low as 3 nmol·L−1 ascorbic acid, 30 nmol·L−1 uric acid, 16 nmol·L−1 glutathione, and 28 nmol·L−1 cysteine. The total antioxidant capacity (TAC) of human serums has been determined in order to assess the feasibility of the CL system. The results of serum TAC, with ascorbic acid as an equivalent model, show a good consistency with those obtained by the standard CUPRAC method. This work not only benefits the rational design of a high catalytic functionality nanozyme, but also constructs a robust TAC detection platform for monitoring oxidative stress-related diseases.

On the Nature of HOPG-Supported Pt1Ti2O7 and its Decomposition of a Nerve Agent Simulant: A Cluster Model of a Single Atom Catalyst Active Site.

Chemical weapons, including hyper lethal nerve agents, are a persistently looming threat across the modern geopolitical landscape. There is a pressing need for the design and development of improved protective materials, which can be substantially aided by the cultivation of a fundamental molecular-level understanding of candidate systems and the corresponding decomposition chemistry. The emergence of the exciting new class of single atom catalyst (SAC) materials has enhanced the prospect of subnanoscale design tailoring in the hopes of optimizing activity and selectivity for a variety of chemical applications. Here, we apply our recently developed experimental technique for modeling the active sites of such SAC materials through the preparation of surface supported size-selected single metal-atom doped metal oxide clusters. The propensity for an SAC cluster model system for Pt1/TiO2 materials, Pt1Ti2O7 supported on highly oriented pyrolytic graphite (HOPG), to adsorb and decompose nerve agent simulant dimethyl methylphosphonate (DMMP) was investigated through a combination of temperature-programmed desorption/reaction (TPD/R) and X-ray photoelectron spectroscopy (XPS). XPS measurements of the as-prepared Pt1Ti2O7 clusters supported the successful isolation of single Pt atoms in clusters monodispersed across the HOPG surface. TPD/R experiments showed that the reactivity exhibited by the Pt1Ti2O7 clusters was distinct from that of Ti2O7 clusters lacking the single Pt atom. It was found that DMMP decomposed over Pt1Ti2O7 upon heating to as low as room temperature, and higher temperature treatments evolved exclusively H2O, CO, and H2, while decomposition over Ti2O7 evolved only methanol and formaldehyde at elevated temperatures. This indicated the promotion of C-H and PO-C bond cleavage within DMMP due to the presence of single Pt atoms in the clusters. Further, the Pt1Ti2O7 clusters were found to desorb P-containing decomposition species, preventing active site poisoning; however, a change of reactivity reflecting that of Ti2O7 was observed following a single TPD/R cycle. This suggested the encapsulation of active Pt sites by titanium oxide during high temperature treatment and is thus an issue deserving of serious attention in the study of Pt1/Ti2O7 SAC materials.

A Review on the Effect of Wood Surface Modification on Paint Film Adhesion Properties

Wood surface treatment aims to improve or reduce the surface activity of wood by physical treatment, chemical treatment, biological activation treatment or other methods to achieve the purpose of surface modification. After wood surface modification, the paint film adhesion performance, gluing performance, surface wettability, surface free energy and surface visual properties would be affected. This article aims to explore the effects of different modification methods on the adhesion of wood coating films. Modification of the wood surface significantly improves the adhesion properties of the paint film, thereby extending the service life of the coating. Research showed that physical external force modification improved the hydrophilicity and wettability of wood by changing its surface structure and texture, thus enhancing the adhesion of the coating. Additionally, high-temperature heat treatment modification reduced the risk of coating cracking and peeling by eliminating stress and moisture within the wood. Chemical impregnation modification utilized the different properties of organic and inorganic substances to improve the stability and durability of wood. Organic impregnation effectively filled the wood cell wall and increased its density, while inorganic impregnation enhanced the adhesion of the coating by forming stable chemical bonds. Composite modification methods combined the advantages of the above technologies and significantly improved the comprehensive properties of wood through multiple modification treatments, showing superior adhesion and durability. Comprehensive analysis indicated that selecting the appropriate modification method was key for different wood types and application environments.

Influence of waste glass and rice husk ash on the dynamic compressive properties and variable-angle shear characteristics of concrete after high-temperature treatment: Experimental and numerical study

This study investigates the use of glass sand, glass powder, and rice husk ash in concrete to mitigate the depletion of natural river sand and cement resources. High-temperature environments were simulated using a muffle furnace, and dynamic compression and variable-angle shear tests were conducted to assess the effects of these recycled materials on the mechanical properties of concrete under normal and high-temperature conditions. Results show that while the dynamic compressive strength of ordinary concrete decreases with increasing temperature, the addition of waste glass and rice husk ash enhances strength and modifies the temperature-strength relationship. Rice husk ash increases the strain rate sensitivity, resulting in higher stress rates and more gradual stress-strain curves. Glass sand concrete exhibited improved energy absorption and resistance to dynamic loads, especially with rice husk ash at elevated temperatures. Additionally, concrete containing glass demonstrated superior cohesion and internal friction angles. An improved plastic damage model was validated through simulations, showing enhanced damage resistance in concrete with rice husk ash at temperatures below 400 °C. This study highlights the potential of waste glass and rice husk ash in improving concrete performance and damage resistance.

High-temperature anaerobic calcination for stabilizing environmentally stressful elements in phosphoric acid production by-products

Phosphorus tailings (P) refer to the waste materials left over after the extraction of phosphorus from phosphate rock during mining and processing. phosphogypsum (PG) is typical by-products of phosphoric acid production (PPB), containing numerous environmentally hazardous elements (EHE) that pose significant risks to ecological safety. In this study, we examined the impact of high-temperature anaerobic calcination on the migration and immobilization of EHE in PPB. The results indicated that higher temperature ranges favorably controlled the leaching toxicity of PPB. In the calcination products of P and PG, the inhibition efficiency of Pb leaching toxicity reached 84.93% and 89.33%, respectively. Under higher temperature conditions (P at 700 °C, PG at 600 °C), the inhibition of Cr leaching toxicity reached 100%. The inhibitory effects of high-temperature environments on EHE in PPB were ranked as fluorine > phosphorus > heavy metals. The mechanisms of migration and transformation of EHE in PPB under high-temperature anaerobic calcination were elucidated in three aspects, ranked from strongest to weakest. Firstly, the encapsulation of EHE by a shell-like structure, attributed to the “melt-wrap” phenomenon. Secondly, the decomposition-gasification phenomenon induced by high-temperature conditions. Thirdly, the effect of high temperature on the transformation of the storage forms of EHE. This study fills a research gap in the field of thermal treatment of PPB, enhancing the understanding of the specific effects of thermal treatment on the transformation of EHE in PPB, and provides theoretical and data support for the high-temperature thermal treatment of solid wastes.

Bifunctional modulation of Li-rich layered oxide cathode material via W-modification for improved electrochemical performance

Lithium-rich layered oxides (LRLOs) have raised the greatest attention to the high-energy-density Li-ion batteries. Nevertheless, the undesirable interfacial side reactions and the structure transformation cause fast voltage fading and poor capacity retention of LRLO cathodes, which extremely prevent their practical application. Surface coating or lattice doping has been an effective strategy to improve its electrochemical properties. However, the general performance of the material can only be limitedly promoted. Herein, we proposed a bifunctional modulation of LRLO cathodes coupled by bulk-phase W-doping and surficial Li2WO4 nanocoating of LRLOs using a facile synchronous lithiation strategy under a high-temperature solid-state treatment. The modified material (2 mol% W6+ modified) showed a distinguished discharge capability of 260.5 mAh/g at 0.1 C after 50 cycles. Meanwhile, a competitive capacity retention of 95.38% at 1 C after 100 cycles was achieved. The splendid electrochemical performance can be the result of the increased interlayer spacing for enhancing Li+ diffusion kinetics and the stronger W–O bond for alleviating oxygen release after W-doping and Li2WO4 nanocoating, which not only accelerates the Li+ transfer rate as its fast Li+ transfer channels but also act as a transitional interface layer to restrain the interfacial adverse reactions.

Preparation of natural adhesives with high-strength and low temperature fast-curing properties

The development of natural adhesives to substitute petroleum-based products is crucial for sustainable progress. However, the bond strength of most existing natural adhesives still falls short of that of commercially available adhesives and the curing process often demands prolonged high-temperature treatment. Herein, we prepared pure natural adhesives using gelatin (GE), tung oil (TO), and dopamine (DA) as the main raw materials. The shear strength of the adhesive to wood reached up to 6.35 MPa, a significant improvement over most natural wood adhesives reported. Additionally, the tensile strength of the adhesive to wood reached 10.50 MPa, which is comparable to commercially available neoprene-phenolic wood adhesives (9.99 MPa) and cyanoacrylate instant adhesives (9.48 MPa). In addition, the natural adhesive prepared by us exhibits fast curing performance at room temperature and can be fully cured in only 12 min, which is significantly better than the commercially available adhesive. The adhesives prepared in this study also possessed excellent reversible curing properties, antimicrobial properties, low toxicity, and degradability. These characteristics offer new insights for the advancement and dissemination of natural adhesives.

Investigation of Precipitation Behavior of a Novel Ni-Fe-Based Superalloy during High-Temperature Aging Treatment.

The precipitation behavior of a novel Ni-Fe-based superalloy developed for advanced ultra-supercritical (A-USC) coal-fired power plant applications during high-temperature aging treatment was investigated. The results showed that the major precipitates in the novel alloy were randomly distributed MC carbides, M23C6 carbides at grain boundaries, and the γ'-Ni3 (Al, Ti) phase in grain interiors after aging. MC remained relatively stable during both short-term and long-term aging. M23C6 quickly precipitated and exhibited a discrete distribution at grain boundaries during short-term aging, and partly developed into continuous films during long-term aging. After uniform precipitation, the shape of γ' remained spherical, and the size kept increasing with aging time according to the Lifshitz-Slyozov-Wagner (LSW) model. The hardness of the novel alloy was mainly associated with the precipitation behavior of γ'; as γ' gradually precipitated, the hardness steadily increased; after complete precipitation, as the size of γ' increased, the hardness first increased and then decreased, reaching the peak hardness when the average radius of γ' achieved the critical size. In addition, the novel alloy exhibited abnormal coarsening behavior at grain boundaries during both short-term and long-term aging. The coarsened grain boundaries were actually precipitate-free zones (PFZs) and the coarsened and elongated rod-like particles inside were identified as γ' precipitates. The mechanism of strain-induced grain boundary migration and the discontinuous coarsening reaction is proposed for the formation of PFZs. Furthermore, PFZs were considered to be potential crack sources during the creep rupture test, leading to earlier failure of the material.

Effect of chitosan oligosaccharides with different molecular weight in alleviating textural deterioration of chicken myofibrillar protein gel with high-temperature treatment

The molecular weight (MW) of oligosaccharides on gel properties of myofibrillar protein (MP) at high temperature remains unclear. In this study, it was found that chitosan oligosaccharides (CO) with different MW all significantly alleviated the textural deterioration of MP gel with high-temperature treatment. Moreover, MP-CO gel with the largest MW had the highest breaking force and the lowest cooking loss. Low-field NMR results further indicated that MP-CO gel with larger MW of CO had gradually increased relaxation rate, thus binding water more tightly. Rheological and microrheological tests suggested the addition of CO with larger MW resulted in much tighter gel network. These results indicated that CO with larger MW improved the quality of MP gel more effectively, which was because CO with larger MW inhibited aggregation of MP to a larger extent, resulting in smaller MP aggregates. Then MP-CO gel with much denser and more homogeneous structure was formed. Besides, MP-CO gel with larger MW of CO had higher content of β-sheet, resulting in MP gel with more ordered structure and better gel quality. Therefore, this study provided theoretical guidance for choosing the appropriate CO in improving texture of high temperature meat products.

Gradual Optimization of Molecular Aggregation and Stacking Enables Over 19% Efficiency in Binary Organic Solar Cells.

Volatile solid additive is an effective and simple strategy for morphology control in organic solar cells (OSCs). The development of environmentally friendly new additives which can also be easily removed without high-temperature thermal annealing treatment is currently a trend, and the working mechanism needs to be further studied. Herein, a highly volatile and non-halogenated solid additive 1-benzothiophene (BBT) is reported to regulate molecular aggregation and stacking of active layer components. According to the film-forming kinetics process, a momentary intermediate phase is formed during spin-coating, which slows down the film-forming process and leads to more ordered molecular stacking in the solid film after introducing solid additive BBT. Subsequently, after solvent vapor annealing (SVA) further treatment, the resultant blend films exhibit a tighter and more ordered molecular stacking. Consequently, the synergistic effect of solid additive BBT and SVA treatment can effectively control morphology of active layer and improve carrier transport characteristics, thereby enhancing the performance of OSCs. Finally, in D18-Cl:N3 system, an impressive power conversion efficiency of 19.53% is achieved. The work demonstrates that the combination of highly volatile solid additives and SVA treatment is an effective morphology control strategy, guiding the development of efficient OSCs.

3D printing of aligned silk fibroin microfibers covered with nitrogen-doped carbon dots for anti-counterfeiting

Counterfeiting has serious economic and social consequences, prompting researchers worldwide to develop innovative and highly secure anti-counterfeiting methods, including the use of various polymer printing techniques and the integration of functional materials to create patterns with customized designs that are easy to detect and cannot be falsified. Composite inks made of silk fibroin microfibers and polyvinyl alcohol or polyethylene glycol were developed to produce patterns with the microstructures aligned in the direction of extrusion during the 3D printing process. Fibroin microfibers were obtained via high temperature treatment and used as a precursor for carbon dot synthesis. This approach allowed the microfiber structure to be maintained and be amenable to the synthesis of carbon dots doped with N-heteroatom on its surface, resulting in a material that fluoresces bright blue when irradiated at 365 nm but remains invisible in normal lighting conditions

Ameliorating the microstructure and properties of a Cu[sbnd]Cr alloy by introducing a high-temperature short-time treatment into the thermo-mechanical process

The optimization of process is essential for improving the overall properties of high-strength and high-conductivity Cu alloys. This study introduces a high-temperature short-time treatment (HTSTT, 850 °C/5 min) into the thermo-mechanical process of a CuCr alloy. Following the process of “solid solution - cold rolling - HTSTT - cold rolling - aging”, the tensile strength of the alloy increases from 450 MPa to 508 MPa, with the electrical conductivity increasing from 82.2 %IACS to 86.4 %IACS when compared to the conventional process of “solid solution - cold rolling - aging” under the same total deformation condition. The reasons for the improvement in the comprehensive properties of the alloy after introducing HTSTT are analyzed through microstructural characterization. The results indicate that the HTSTT promotes the occurrence of recrystallization, leading to grain refinement, which results in smaller grain sizes during subsequent processing. Additionally, the introduction of HTSTT changes the main texture of the alloy from 〈100〉//X to 〈111〉//X during the process, which is beneficial to enhancing the alloy's strength and electrical conductivity. More importantly, the HTSTT facilitates the precipitation of solute Cr atoms, leading to the formation of a significant quantity of nanoscale Cr particles, most of which are spherical with an average size of 27 nm. During the subsequent cold rolling process, these Cr particles effectively pin dislocations and promote their proliferation, leading to the precipitation of a large number of smaller Cr particles during the aging process, with an average size of 4.8 nm. These finer Cr particles are crucial for precipitation strengthening. This paper offers valuable insights into the microstructural optimization and performance enhancement of high-strength and high-conductivity Cu alloys.

Effect of surface treatment on oxidation film of 55SiCr spring steel wire

Abstract In this work, the surface pretreatments of 55SiCr spring steel wire rods were conducted using shot blasting and phosphating. After drawing, the steel wire was heated at 950°C × 15 s, followed by oxidation treatment with high-temperature steam or air for 3 seconds, and tempering treatment at 520°C. The effects of different surface treatment methods on the surface oxide film of spring steel wire were studied using stereomicroscopy, SEM, EDS, and XRD. The results showed that the steel wire surface oxide film with phosphating pretreatment was thicker and easy to fall off. The thickness of the oxide film formed by phosphating pretreatment samples increased by 2.1 um (high-temperature steam) and 0.3 um (air) compared to the shot-blasting samples under different oxidation atmospheres. High-temperature steam oxidation treatment significantly increased the thickness of the oxide film by 0.65 um (shot blasting) and 2.45 um (phosphating) under different surface pretreatment conditions. The outer surface of the oxide film turned black with high-temperature steam oxidation treatment and turned yellowish brown with air oxidation treatment. By both above oxidation treatments, the oxide film showed a multilayer structure, with enrichment of Cr and Si on the inner side.