High Temperature Aging Research Articles

Polymers marry with carbon nanospheres: A promising strategy to develop high-performance filtrate reducer

Polymeric filtrate reducers have limited uses under high temperature and salinity conditions. The incorporation of nanoparticles to polymeric networks is a popular and effective method for creating high-performance filtrate reducers. However, present nanofillers are costly, have negative environmental consequences, and are difficult or impossible to disseminate. Herein, a simple hydrothermal process using low-cost and renewable glucose as raw ingredients resulted in hydroxy-rich carbon nanospheres (CNs). After modification by acryloyl chloride, the CNs were copolymerized with acrylamide, 2-acrylamido-2-methylpropanesulfonic acid, and sodium p-styrene sulfonate. The obtained CNs-doped polymers (CAAS) were able to maintain high viscosity and colloidal stability even after salt contamination and high temperature aging. CAAS-based drilling fluids can tolerate temperatures of up to 240 °C under 30% NaCl conditions. The API filtration loss (FLAPI) and the high-temperature high-pressure filtration loss (FLHTHP) were 10 and 63.5mL, respectively. Considering the low-cost and renewable raw materials, high dispersibility and high compatibility of CNs as well as significant improvement in thermal-resistance and salt-tolerance, this work provides a simple yet effective approach to developing high-performance filtrate reducers for complex geological conditions.

Deep learning assisted prediction on main factors influencing shear strength of sintered nano Ag-Al joints under high temperature aging

Bonding strength of sintered nano silver (Ag) joints has been an important index for evaluating the reliability of power module packages, which has been reported to be influenced by many factors. However, it is hard to evaluate and predict those factors affecting bonding strength. With the help of artificial intelligence (AI), the utilization of AI tools to assist in finding science solutions has become a mainstream consensus. In this paper, we will show how to evaluate and predict those sintered nano Ag-Al bonded joints bonding strength with deep learning (DL) methods. Firstly, a reliable extended dataset was obtained using the conditional formal condition table generation Induction Network (CTGAN) based on the die shear test dataset of sintered Ag-Al interface shear strength with four different metallization layers under different high-temperature aging time. Subsequently, four DL models were adopted to predict the shear strength of Ag-Al interface under different metallization layers to evaluate the interface bonding strength, all with high level of determination coefficient (R2, above 0.99) and classification accuracy (above 85%). Last but not least, factors influencing the shear strength of Ag-Al interface were analyzed and ranked by weight analysis and SHapley Additive exPlanations (SHAP) method. This research could provide a novel perspective on understanding those factors affecting the shear strength of sintered nano Ag interconnect layer in power devices.

Thermosensitive polymer/nanosilica hybrid as a multifunctional additive in water-based drilling fluid: Rheologicalproperties and lubrication performance as well as filtration loss reduction capacity

In previous studies, for obtaining a flat rheological drilling fluid, binary and ternary thermosensitive silica (SiO2) nanohybrids as rheological modifiers were synthesized using N-isopropylacrylamide with a thermal association temperatureof 32–33 °C as the thermosensitive monomer [J. Petrol. Sci. Eng. 219 (2022), 111096; Geoenergy Science and Engineering 228 (2023), 211934]. However, the as-synthesized SiO2 nanohybrids exhibited limited performance and low thermal transition temperature. Thus surface initiated atom transfer radical polymerization was utilized to graft hydrophilic poly(ethylene glycol) methyl ether methacrylate (PEGMA) onto SiO2 surface to obtain PEGMA/SiO2 nanohybrids with an elevated thermal association temperature of 75 °C. The morphology and structure of the as-synthesized PEGMA/SiO2nanohybrid were characterized by infrared spectroscopy and transmission electron microscopy; and its effects as a thermosensitive multifunctional additive on the rheological properties and lubrication performance as well as filtration loss reduction capacity of a water-based drilling fluid were investigated. Results indicate that the drilling fluids with 1.0% PEGMA/SiO2 nanohybrids exhibited obvious thermal thickening behavior in the temperature range of 70–80 °C; at low temperatures, however, they had a significant viscosity reduction effect therein. At room temperature, the apparent viscosity and plastic viscosity were reduced by 68% and 50%, respectively. Besides, due to the tightly packed plugging layer formed by PEGMA/SiO2 nanohybrids and bentonite, the filtration loss of the drilling fluids containing 1.0% PEGMA/SiO2 nanohybrid was reduced by 37% as compared with that of the base slurry; and the lubrication coefficient was decreased by up to 50%. Moreover, the high-temperature aging process promoted the intermolecular interactions of the nanohybrids and their interaction with bentonite flakes, thereby further improving the rheological behavior, filtration reduction ability, and lubricity of the drilling fluids. The as-synthesized thermosensitive PEGMA/SiO2 nanohybrids with excellent multifunctionality could find promising application in water-based drilling fluids.

Preparation of molybdenum disulfide/bentonite nanohybrid and its tribological properties as lubricant for water-based drilling fluids

In recent years, with the increase in energy demand and gradual scarcity of medium and shallow oil and gas resources, oil and gas exploration has shifted to special wells such as deep wells, ultra-deep wells, and extended reach wells. These complex wellbore structures inevitably increase the torque and friction between the casing and the drill pipe during drilling, which aggravates friction and wear, and leads to accidents such as drill sticking and drill breakage in severe cases. In this study, molybdenum disulfide/bentonite (MoS2/Bent) nanohybrids as drilling fluid lubricant were synthesized by hydrothermal method using sodium molybdate (Na2MoO4) and thiourea (CH4N2S) as raw materials and bentonite as carrier. The as-synthesized MoS2/Bent nanohybrid was characterized by X-ray powder diffractometer, transmission electron microscopy, Fourier transform infrared spectroscopy, and the high temperature resistance and tribological properties of MoS2/Bent nanohybrid were evaluated in base slurry. The results show that the friction coefficient of MoS2/Bent nanohybrid drilling fluid before aging is reduced by 74 % and the wear rate is reduced by 97 % compared with the base slurry. After high-temperature aging at 240 °C, the friction coefficient is reduced by 77 % and the wear rate is reduced by 90 %. The excellent friction reducing and antiwear performance is attributed to the formation of low shear strength MoS2 deposition film and oxide tribofilm on the surface of the friction pair during the rubbing process.

Glass-based encapsulant enabling SiC power devices to long-term operate at 300 °C

The high-temperature applications of Silicon Carbide (SiC) power devices are constrained by traditional epoxy molding compound (EMC). A significant challenge arises from the mismatch between the thermal expansion coefficients (CTE) of the encapsulant and the SiC chip, generating thermal and mechanical stresses during prolonged high-temperature operation. While glass encapsulants offer stability above 300 °C, these stresses can lead to mechanical degradation and eventual failure of SiC power devices. We design a glass-based encapsulation material to adjust the CTE of the glass to match that of the SiC chip (3–9 ppm/℃), enabling encapsulation of the device for long-term operation at 300 °C. Finite element analysis (FEA) confirms that the CTE adjustment effectively reducs internal thermal stresses. The glass composite with 10 wt% PbTiO3demonstrates a Tg of 310 °C and a CTE of 8.48 ppm/℃, successfully encapsulating a SiC schottky barrier diode in TO-247 package form. The encapsulated device exhibits low leakage current, a reverse breakdown voltage of 1,700 V, and a thermal resistance of 0.45 °C/W. Notably, the device maintains excellent performance even after 1,176 h of high-temperature aging, including 336 h at 300 °C and exhibits minimal change during thermal cycling between −50 and 150 °C for 100 cycles. Long-term performance analysis demonstrates superior stability compared to EMC encapsulation. These results highlight the potential of glass-based encapsulants for wide band gap power devices, offering reliability and performance under extreme conditions.

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.

Experimental and first-principles novel insights of atomic collapsed structure and composition-driven ω-precipitates

A complex ω phase transition is often observed in titanium alloys; nevertheless, the underlying knowledge of ω-embrittlement are not yet fully understood and require deeper insight. In this study, the ωT and ωH phases, as well as their interfacial structures, have been systematically investigated to examine compositional partitioning and to estimate Z values. A combination of aberration-corrected HAADF-S/TEM advanced characterization techniques, together with first-principles density functional theory calculations were performed under various heat treatment conditions. The results revealed that the low-temperature ageing process suppresses ω-assisted secondary α precipitations at ωT/β interfaces, whereas high-temperature ageing process promotes ω-assisted secondary α precipitations at ωH/β interface, due to relatively higher concentrations of Mo and Al contents. The interfacial energies (γ{ωβ}) between β and ω phases increase with decreasing local compositions of Mo and Al, suggesting increased stability of the ω phase and decreased stability of the β phase. Furthermore, the formation energies of β and ω phases were computed with Mo content at different Al composition, results indicate that the ω phase transition process is affected by the reduced Al content. The observations of this work provide deeper understanding of the ω phase transition mechanism in titanium alloys.

Titania-Based Coral-Structured Solar Absorber Coating with Improved Scalability and Durability at High Temperature.

Solar energy harvesting and storage are essential in the future mix of renewable energy technologies. Hierarchical coral-structured coatings have been shown to yield high solar absorptance in concentrating solar thermal (CST) systems. However, interfacial delamination and scalability challenges owing to material complexity pose significant hurdles for the widespread industrial adoption of these hierarchical CST coatings. Here, a coral-structured coating is proposed whose black pigments are strongly bonded by titania, which is a material that mitigates interfacial delamination. Importantly, this coating follows a facile deposition procedure suitable for large-scale solar receivers. The drone-deposited coating inhibits cation diffusion and maintains a stable solar absorptance of even after long-term (3000 h) high-temperature ( ) aging. The scalability of developed coating represents a substantial advancement in the implementation of light-trapping enhancement and maintenance approaches across a wide range of CSTapplications.

Research on aliphatic resin-reinforced bamboo spun fiber bundles based on optimal twisting process

Bamboo, recognized as a sustainable material with remarkable properties, has found extensive application in the textile industry. This paper presents the findings of an investigation into the mechanical properties of twisted bamboo spun fiber bundles. The bundles were produced through the delignification and thinning of moso bamboo, followed by twisting in both the Z-direction and the S-direction, with varying twisting angles as experimental variables. The results indicated that the mechanical properties of the bamboo spun fiber bundle, produced under a single-strand Z-twist direction with a 20° twist angle, were optimal. These properties included the highest tensile strength of 154.25 MPa, a low modulus of elasticity, and a high elongation at break of 6.9 %, which represented superior preparation parameters. To enhance the bamboo spun fiber bundles during the preparation process—particularly because they tend to absorb moisture easily and disintegrate due to the removal of some lignin—a mixture of aliphatic epoxy resin and amine curing agents is employed. Following resin impregnation, both the expansion rate and orientation of the bamboo spun fiber bundles demonstrated a reduction compared to the unimpregnated one. The epoxy resin conferred dimensional stability and flexibility to the fiber bundles. Additionally, compared with those without impregnation, resin-impregnated bamboo spun fiber bundles resulted in a strength increase of 6.81 %, an enhancement in elongation at break of 9.79 %, a reduction in modulus of 2.67 %, a small plastic deformation of 13.96 % under cyclic loading, and a decrease in performance of only 3.5 % after high-temperature light ageing. This material demonstrated improved strength, toughness, and durability, aligning more closely with the requirements for textile fiber raw materials. The findings of this study refine processing parameters and broaden the application of bamboo spun fiber bundles in home furnishings and decorative contexts.

External short circuit of lithium-ion battery after high temperature aging

The microscopic and macroscopic changes of lithium-ion batteries after high temperature cycling and their effect on external short circuit (ESC) are studied in this study. The results indicate that solid electrolyte interphase and cathode electrolyte interphase cover the surface of anode and cathode. Transition metal, Mn is dissolved from the cathode. Capacity and resistance decreases and increases after cycling at high temperature. The safety of batteries after ESC is ranked as: 70 % state of health (SOH) > 100 % SOH > 80 % SOH > 90 % SOH. Thermal runaway only occurs to battery with 90 % SOH after ESC. Increase of resistance after cycling affects heat generation during ESC less. Onset temperature and thermal runaway temperature increases and decreases owing to solid electrolyte interphase growth and Mn dissolution. Compared to fresh battery, safety of battery with 70 % SOH after ESC increases. Fast discharging causes side reactions for aged batteries, which also generate heat. The heat generation effect of fast discharging decreases with the decrease of SOH after 90 % SOH. Local micro internal short circuit causes more heat generation for aged batteries. The results are important for safety control of lithium-ion battery.

In-situ formed stable Pt nanoclusters on ceria-zirconia solid solutions induced by hydrothermal aging for efficient low-temperature CO oxidation

Pt nanoclusters (PtC) on the surface of ceria-zirconia solid solutions exhibit superior low-temperature CO oxidation activity compared to Pt single atoms (Pt1). However, the redispersion behavior of the PtC to Pt1 lowers the efficiency of CO Oxidation. In this work, the stable surface hydroxyl groups were constructed by high-temperature hydrothermal aging treatment. Specifically, the Pt1 catalyst (Pt/CZOe-SA) prepared by atom trapping was subjected to high-temperature hydrothermal treatment to obtain the stable PtC catalyst (Pt/CZOe-HT) with in-situ formed PtC. The experimental results showed that PtC with 2–3 nm size could achieve excellent low-temperature activity and thermal stability. In addition, the ab initio molecular dynamics and density functional theory calculations revealed the specific evolution process of dynamic dispersion for PtC with or without hydroxyl groups from the femtosecond scale, suggesting that the hydroxyl groups limited the dispersion of PtC in the form of “energy fence”. The hydrothermal treatment not only introduced high-temperature stable hydroxyl groups to improve the stability of the in-situ formed PtC, but also optimized the ratio of Pt1 and PtC, and then enhanced the low-temperature activity by the synergistic effect between Pt1 and PtC. The present work can provide theoretical guidance for developing high-performance and high-stability Pt-based catalysts.

Insights into the swelling force in commercial LiFePO4 prismatic cell

Lithium-ion batteries undergo reversible and irreversible swelling force during cycling. The mechanical behavior and swelling force of lithium-ion batteries are important in practical applications. In this study, the variation and the aging mechanism of swelling force, and the growth pattern under different cycling conditions have been studied with commercial cells. The findings reveal distinct dynamic stress peaks corresponding to the state of charge (SOC) increase, indicative of notable lattice expansions in both cathode and anode. This expansion intensifies over cycles, with the most significant escalation observed at 30 % SOC, gradually assuming a pivotal role in battery expansion dynamics. Post-mortem analysis, coupled with stress-strain evaluations, attributes this phenomenon primarily to moduli variations across SOC during the aging process. Moreover, the trajectory of swelling force amplification varies across aging paths, with high-temperature cycling demonstrating accelerated growth. This accelerated growth stems from the broadened expansion of battery components beyond solid electrolyte interphase (SEI) formation induced by high-temperature aging.

Characterization of temperature regulating, high-temperature rheological and anti-aging properties of asphalt mastic modified with SSPCMs

The objective of this study is to explore the potential of utilizing self-developed SSPCMs as additives for heat storage temperature regulation in asphalt mastic modification. To achieve this aim, a variety of asphalt mastics with different F-A volume ratios and SSPCM contents were formulated, and their high-temperature rheological properties, modification mechanisms, thermoregulation capabilities, and aging resistance performances were analyzed. The results of temperature regulation test indicated that the maximum cooling amplitude of asphalt mastic could reach 11.3°C, showing a great promising application for cooling asphalt pavements. Additionally, the incorporation of SSPCMs generally resulted in positive impacts on both the high-temperature rheological properties and temperature sensitivity of the asphalt mastics. Moreover, the aging indices GAI, ICO and ISO of the modified asphalt mastic with 30 % SSPCMs decreased by 5.6 %, 18.3 % and 8.7 %, respectively, compared with control asphalt mastic, implying that the incorporation of SSPCMs can retard the aging process of asphalt and enhance the thermal oxidative aging resistance of the asphalt mastics. In summary, the current study demonstrates the feasibility, improved performance, and effective thermoregulation properties of SSPCMs in asphalt mastics.

Enhancing structural strength and water retention of crosslinked polyacrylamide gel with the T-ZnOw

Crosslinked polyacrylamide gel serves as an effective plugging material, crucial for preventing water/gas channeling in reservoirs and enhancing the swept volume and oil recovery. However, its practical application encounters a significant challenge in maintaining long-term stability of strength and volume, particularly under high temperatures. This study investigates the reinforcement of polyacrylamide gel with three-dimensional (3D) nanomaterials, specifically tetra-needle-like zinc oxide whiskers (T-ZnOw), to enhance its structural stability and bound water content. The stress sweep tests showed that the addition of 0.15 wt% T-ZnOw increased the maximum elastic modulus of the gel to 28.5 Pa, representing a 51.2 % improvement compared to before the addition. After 60 days of high-temperature aging at 130 °C, the T-ZnOw strengthened gel still maintained an elastic modulus of 21.8 Pa. With increasing T-ZnOw concentration, the yield point of the gel increased from 4.74 Pa to 9.57 Pa, the anti-deformation of the gel has significantly increased. The stability test results in high salinity water indicate that at a salinity of 150,000 mg/L, the dehydration rate of the strengthened gel is less than 5 %, with an elastic modulus retention rate exceeding 88 %. Furthermore, thermodynamic testing confirms the enhanced thermal degradation resistance and water retention capacity of the gel. Under reservoir temperature conditions, the T-ZnOw strengthened gel exhibits a weight loss of less than 3 %. Additionally, the inclusion of T-ZnOw results in an increase in the bound water capacity index from 4.65 to 12.28. In conclusion, the integration of T-ZnOw into the polyacrylamide gel network not only enhances its mechanical performance and water retention under high-temperature conditions but also demonstrates superior stability in high-salinity environments. This innovative material shows significant potential for improving oil recovery rates in high-temperature reservoirs and can be applied to other high-temperature underground scenarios such as geothermal development and CO2 utilization and storage.

Effect of aging temperatures on the microstructure and mechanical properties of TC21 forgings with basket–weave microstructure

This study aims to explore the influence of various aging temperatures on the microstructure and mechanical properties of TC21 forgings. Basket-weave microstructures were prepared via quasi-β forging followed by annealed at 900 °C for 1.5 h and aged at 530 °C, 560 °C, and 590 °C for 4 h, and then their tensile performance, impact toughness, and fracture toughness were examined. Results indicate that higher aging temperatures not only facilitate the segregation of Al element, resulting in a reduction in the effective size (dαlaths, the width/length ratio) of primary α laths (αlaths) and their amount, but also promote phase transition, inducing an increase in the effective size (dαfine) of secondary fine α (αfine) lamellae. While both dαlaths−1/2 and dαfine−1/2 have a linear relationship with the strength, which was analyzed using the Hall–Petch relationship, the more pronounced interface strengthening effect and hindering crack propagation mainly results from the αlaths. Moreover, the plasticity declines significantly as the proportion of the αlaths phases decreases. Thus, for strength and plasticity, the αlaths are a much more important factor than the αfine lamellae. However, although the synergistic deformation and fracture of both the αlaths and αfine phases can consume a larger impact initiation energy, the enhancement of the impact energy of the alloy is primarily related to a high precipitation amount of the αfine lamellae. Furthermore, the decrease in dαlaths promotes the misorientation and accumulation of dislocations between αlaths interfaces, hindering the enhancement of KIC (fracture toughness) by forming transgranular fractures. Conversely, the increase in KIC attributed to the energy consumed in the plastic deformation region at the crack tip, due to the αfine lamellae compensates for the energy, resulting in a reduction in the crack propagation path. Therefore, the αfine lamellae may play a more crucial role in increasing the toughness of alloys, in particular the impact toughness of the TC21 alloy.

Thermal Treatment Effects on Structure and Mechanical Properties of Polybutylene Terephthalate and Epoxy Resin Composites Reinforced with Glass Fiber.

In this study, two types of composites, polybutylene terephthalate (PBT) and epoxy resin (ER), reinforced with 20% of glass fiber (GF) are used as the comparative research objects. Their mechanical properties after thermal aging at 85~145 °C are evaluated by tensile strength and fracture morphology analysis. The results show that the composites have similar aging laws. The tensile strength of GF/PBT and GF/ER decrease gradually with the increase of aging temperature, while their elastic moduli are independent of the thermal treatment temperature. Scanning electron microscopy study of the fracture surface shows that separation of glass fiber from PBT and ER matrix becomes more obvious at higher aging temperature. The fibers on the matrix surface appear clear and smooth, and the whole pulled out GFs can be observed. As a main mechanical strength degradation mechanism, the deterioration of interface adhesion between the matrix and GF is discussed. A large difference in coefficients of thermal expansion of the matrix and GF is a main factor of the mechanical degradation.

Determination of Electrochemically Active Surface Area in All-Solid-State Batteries

All-solid-state batteries (ASSBs) are currently receiving much attention as one of the most promising next-generation rechargeable battery systems due to their promise of high energy density and high safety. Despite many efforts to commercialize ASSBs, however, there are still many unresolved technical challenges. Unlike conventional lithium-ion batteries (LIBs), the interface between the cathode and electrolyte in ASSBs exhibits a complex degradation pattern that combines chemical and mechanical degradations. In particular, the high Ni content cathode materials in ASSBs are commonly known to suffer from significant additional degradation mechanism, e.g., volume expansion/contraction due to H2-H3 phase transitions at high voltages, resulting in particle cracking. This degradation of the integrity of the active material leads to a reduction in electrochemically active surface area (active area afterward) due to loss of contact between the active material and solid electrolyte, slow diffusion rate of lithium in the active material, and isolation of the active material. These issues are recognized as major contributors to cell performance degradation. Among these issues, the changes in the active area have a decisive impact on the rate of redox reactions that are key to battery charging and discharging kinetics, so accurate determination of the active area is crucial for the diagnosis and improvement of batteries. In the electrochemical analysis of ASSBs, the poor contact between the solid electrolyte and the active material, or the change of the contact properties during the battery operation, should be a very important consideration. Especially when determining kinetic factors such as charge transfer resistance and chemical diffusion coefficient of cathode material by electrochemical methods, the models we usually use include the electrode surface area value as an important variable, so the accurate estimation of the active area is indispensable for obtaining reliable electrochemical properties. Unlike typical LIBs, in ASSBs the active material/electrolyte interface contact properties change relatively significantly during repeated cycling, so devising a reliable technique to analyze the active area of active materials in ASSBs is very crucial for the research and development of ASSBs. However, to the best of our knowledge, there are still very few studies on this.In this study, we propose promising methods to measure the contact characteristics between the cathode material and the solid electrolyte in ASSBs, namely the electrochemically active surface area, and discuss their reliability based on intercomparison and literature reports. For this purpose, first, the method for determining the active area of active materials based on galvanostatic intermittent titration technique (GITT) and electrochemical impedance spectroscopy (EIS) reported in conventional LIBs was reviewed. Then, its applicability to ASSBs was explored, and a way to improve the reliability of the analysis was proposed. Specifically, a three-electrode cathode half-cell experiment was conducted to analyze the active area of the Ni-rich cathode. The active area was calculated by comparing the diffusion coefficient measured by EIS with that obtained by GITT. When comparing the active area determined at different voltages, it was observed that the active area varies significantly with voltage most likely due to the volume change caused by the H2-H3 phase transition. The second electrochemical method performed for the determination of the active area of the active material is based on the quantification of the lithium intercalation sites on the cathode surface based on the analysis of the frequency factor in Arrhenius expression. For this purpose, battery at different charge states were kept at high temperatures for long periods of time to induce interfacial degradation. The temperature-dependent charge transfer resistance was then determined by EIS analysis, which was used to interpret the redox (or lithium absorption/desorption) reactions kinetically. The experimental results showed that the redox reaction rate followed exactly the Arrhenius relationship for all the charge states used, but the activation energies and frequency factors changed differently depending on the charge state. In this study, we discuss these results in relation to various phenomena that may occur during high-temperature aging, such as the formation of rock salt structures and cracks on the nickel-rich cathode surface, and try to estimate the change in active area. In this study, the electrochemical analysis methods of the contact characteristics between the cathode and the solid electrolyte in ASSBs will be examined in depth and their reliability will be assessed. In addition, further improvements in active area analysis techniques for active materials in ASSBs will be discussed.

High-temperature aging and long-term mechanical properties of polyphenylene sulfide composites for marine use

ABSTRACT Advanced polymeric composites and manufacturing techniques promote developments of marine structures significantly (e.g., spare parts supply chain of shipbuilding and maintenance). In this paper, the GNP/CF-PPS (graphene nanoplatelets short carbon fibre polyphenylene sulfide composite) samples are prepared by mechanically mixing CF-PPS plastic pellets and GNP particles. The mixed compound is 3D-printed by material extrusion additive manufacturing, and the bending mechanics test is carried out to explore how nanoreinforcement affects the ability of printed composites to perform under high temperature conditions. The results show that CF-PPS and GNP/CF-PPS samples have the highest flexural strength at room temperature. As the temperature rises to 260°C, the stiffness increases by 4.8% and 6.7% respectively, while the deflection decreases by 30.4% and 25.6% respectively. The characterisation results of scanning electron microscopy (SEM) show that the cross-sectional pores of CF-PPS samples after adding GNP are relatively reduced, indicating the improvement in the structural stability.

Effect of reactive fumes suppressant DOPO on the chemical composition and performance of asphalt

9,10-Dihydro-9-oxa-10-phosphorophenanthrene-10-oxide (DOPO), recognized for its role as an efficacious fume suppressant, has been shown to mitigate the emission of noxious vapors emanating from asphalt. However, the comprehensive influence of DOPO on the composition and properties of asphalt had remained unexplored. This study embarked on an in-depth examination of the effects of various DOPO dosages on the chemical composition of asphalt, employing hydrogen nuclear magnetic resonance spectroscopy (1H NMR) alongside an exhaustive analysis of asphalt components. Furthermore, the investigation elucidated the consequences of different DOPO dosages on the physical, rheological properties, and aging resistance of asphalt. The results of 1H NMR and component analysis of asphalt disclosed that DOPO engaged in chemical reactions with the unsaturated groups within the asphalt, catalyzing a metamorphosis of saturates into aromatics and resins. Such chemical transformations were instrumental in augmenting the softening point, viscosity, and rutting propensity of the asphalt while imposing a minimal impact on its penetration and ductility. Post exposure to the thin film oven test (TFOT), pressure aging vessel (PAV), and ultraviolet (UV) aging, the DOPO modified asphalt (DMA) exhibited a diminution in the increment of softening point and viscosity aging index relative to the control asphalt. Furthermore, the DMA showcased enhanced retention rates of penetration and ductility, coupled with substantially reduced shifts in complex modulus and phase angle post-aging, underlining its superior aging resistance. Fourier transform infrared spectroscopy analysis revealed a comparatively slower rate of change in carbonyl and sulfoxide groups in DMA after aging, as opposed to the control asphalt. Notably, DMA exhibited enhanced resistance to UV aging relative to TFOT and PAV aging scenarios, a trait attributable to remarkable UV absorption capabilities of DOPO. Fundamentally, DOPO enhanced the high-temperature performance and aging resistance of asphalt while simultaneously diminishing the emission of noxious fumes.

Durability of partially cured GFRP reinforcing bars in alkaline environments with or without sustained tensile load

Corrosion of steel reinforcing bars (rebars) in reinforced concrete structures can be addressed by using corrosion-resistant materials like Fiber-Reinforced Polymers (FRP). However, in France, FRP rebars are primarily restricted to temporary applications due to lack of comprehensive durability data. While numerous studies have explored FRP durability in alkaline environments, understanding the combined effect of alkali ions and sustained loading remains limited. Furthermore, the impact of incomplete matrix curing on the long-term performance of FRP rebars is limited.Accordingly, this paper investigates the durability of Glass FRP (GFRP) rebars exposed to alkali environments at varying temperatures. A batch of partially cured rebars was selected for this study, with part of them undergoing post-curing to investigate the effect of curing state on the ageing behaviour. Additionally, some partially cured specimens were subjected to combined sustained tensile loading at 20 % and 40 % of ultimate strength. Mechanical, physico-chemical and microstructural characterizations were conducted after various exposure durations. Results revealed that incomplete curing minimally impacted long-term tensile properties but significantly affected the interlaminar shear strength of aged rebars. Moreover, applying a combined load had little influence on residual properties at 20°C but led to rapid reduction in GFRP residual tensile strength at higher ageing temperatures (40 and 60°C).