Lifetime Of Materials Research Articles

Circular Consumption Practices as Matters of Care

AbstractWhile a circular economy (CE) paradigm shift has gained significant momentum among academics, practitioners, and policymakers, theory regarding its social aspects remains scant, especially theory based on an ethical, micro-level perspective. Circular consumption, referring to those consumption practices that aim to extend the lifetimes of objects and materials, involves ethical considerations. However, everyday circular consumption and its ethics have not gained a foothold in the CE literature. This article builds on the existing circular consumption literature by drawing insights from the posthuman feminist theorising of care, shifting the focus of care from humans to the complex relations between humans and nonhumans and conceptualising circular consumption practices as matters of care. This conceptualisation, which follows a thinking-with-theory approach, is based on empirical material constructed in two research projects focusing on frontrunner consumers in terms of circular consumption in Finland: food waste reduction and circular clothing consumption. We identify circular consumption as care by introducing three distinct perspectives: care as tinkering, care as affective practices, and care as ethico-political action. We show that approaching circular consumption practices as matters of care, while not always easy or straightforward, is an attempt to make consumption better: more attentive, inclusive, durable, and enjoyable. Our findings emphasise the interconnected nature of circular practices, the constant performativity of circular consumption, and nonhumans as crucial stakeholders in care relations. Consequently, we offer an alternative to technocentric CE perspectives and a way to promote a sustainable world through care.

Post-mortem analysis of material deposition and fuel retention on the plasma-facing materials after the 2021 campaign in EAST

Plasma-wall interaction (PWI) is a critical concern in tokamaks because of its significant impact on the lifetimes of plasma-facing materials (PFMs), fuel retention, and plasma performance. In 2020, the Experimental Advanced Superconducting Tokamak (EAST) PFMs were upgraded to predominantly metallic walls. Following the 2021 experimental campaign, the deposition distribution and fuel retention on the surfaces of the PFMs along both the poloidal and toroidal directions were analyzed. The poloidal tests commenced at the high-field side (HFS), proceeded to the lower divertor, then to the low-field side (LFS), and finally to the upper divertor. The toroidal tests were performed at the midplane of the HFS, beginning from port A and ending at port P. The distributions of the deposits in the poloidal and toroidal directions were clearly asymmetrical. Mo and Fe particles sputtered from the first wall and inner stainless steel (SS) components were prone to deposition in the lower divertor region, as evidenced by the fact that the elemental content in the far-SOL region of the inner divertor exhibited Mo and Fe peaks, as did both the near- and far-SOL regions of the outer divertor. In addition, quick re-deposition of W and Fe was observed, as demonstrated by the fact that their contents near the erosion sources were higher than those farther away along the toroidal first wall on the HFS. This tendency was stronger for W than for Fe. Further analysis indicated that the deposits consisted of Li, C, O, W, Mo, Fe, Cu, and Ni. The Li and Fe contents were much higher than those of other metal impurities, with peak values of 8.17 μg/mm2 and 7.78 μg/mm2, respectively. The Li content decreased along the HFS first wall from 8.17 μg/mm2 at P-2 to 1.82 μg/mm2 at P-22, and then increased to 2.72 μg/mm2 at P-32 in the divertor, while the Fe content was higher around the top side and the midplane of the HFS. The deposited Li originated from routine wall conditioning and existed primarily in the form of Li2CO3. Additionally, other metal impurities deposited on the Li2CO3 surfaces exhibited various irregular shapes, often appearing as aggregated and recrystallized small particles. Furthermore, significant deuterium (D) retention on the order of 1021 atoms/m2 was measured on all the analyzed SiC-coated graphite tiles on the HFS. The D content at location P-10 at the midplane was the highest along the poloidal direction of the HFS because it was directly facing the NBI beam.

Optimizing Molecular Passivation in MAPbI3 Perovskites: Impact of Dipole Moments and Structural Parameters.

In the realm of perovskite materials, organic molecules situated at the A site play a critical role in stabilizing the structure through specific orientations and weak interactions with the inorganic framework. These polar interactions significantly influence the optoelectronic properties of perovskites, and the introduction of polar molecules can disrupt the inherent polarization, thereby altering the material performance. The research primarily focuses on the relationship between the length and width of these organic cations and their polar inductive effects. Overall, the interplay between the chain length, molecular width, and dipole moments was shown to significantly affect the lifetime of MAPbI3 materials. Key findings indicate that non-radiative recombination, which is a major energy loss mechanism in solar cells, is intrinsically linked to the variations of hydrogen bonds and PbI6 octahedral distortion. The analysis revealed a strong negative correlation between octahedral angles, highlighting the complex relationship between these variables and their collective effects on charge carrier dynamics.

Thermal degradation of polytetrafluoroethylene, modified polytetrafluoroethylene, and their nanocomposites with boron nitride nanobarbs: Lifetime predictions and kinetic analysis

AbstractFlexible polymeric materials including dielectric thermal interface materials (TIMs) used in integrated circuits and other high frequency applications are exposed to extreme thermal and electrical conditions during their service life. Insight into the in‐use thermal stability and material lifetime is valuable to maintaining performance durability and preventing premature failure in actual end use. Herein, the thermal stability of polytetrafluoroethylene (PTFE), modified PTFE and their nanocomposites with recent generation boron nitride nanobarbs (BNNBs) was investigated based on lifetime prediction from thermogravimetric analysis and tensile strength deterioration of heat‐aged samples. Additionally, thermal degradation kinetics and mechanism was investigated using the model‐free advanced isoconversional method based on changing activation energy. The result shows that BNNB extends the lifetime of the PTFE by an order of magnitude. The degradation mechanism proposed from TGA‐MS result is supported by the multistep degradation mechanism identified in the kinetic computation. These results are valuable for predicting materials' in‐use lifetime to avoid premature failure.

Polymer-Based Room-Temperature Phosphorescence Materials Exhibiting Emission Lifetimes up to 4.6 s Under Ambient Conditions.

The long-emission-lifetime nature of room-temperature phosphorescence (RTP) materials lays the foundation of their applications in diverse areas. Despite the advantage of mechanical property, processability and solvent dispersity, the emission lifetimes of polymer-based room-temperature phosphorescence materials remain not particularly long because of the labile nature of organic triplet excited states under ambient conditions. Specifically, ambient phosphorescence lifetime (τP) longer than 2 s and even 4 s have rarely been reported in polymer systems. Here, luminescent compounds with small phosphorescence rate on the order of approximately 10-1 s-1 are designed, ethylene-vinyl alcohol copolymer (EVOH) as polymer matrix and antioxidant 1010 to protect organic triplets are employed, and ultralong phosphorescence lifetime up to 4.6 s under ambient conditions by short-term and low-power excitation are achieved. The resultant materials exhibit high afterglow brightness, long afterglow duration, excellent processability into large area thin films, high transparency and thermal stability, which display promising anticounterfeiting and data encryption functions.

Impacts of Photooxidation on Commercially Available Homo and Copolymers of Polypropylene on Their Microstructure and Mechanics: A Cross‐Sectional Analysis

ABSTRACTPolyolefin degradation is widely studied to assess the lifetime of packaging materials. In this work, a combination of bulk (DSC, GPC, 13C‐NMR, XRD), surface (FTIR) and cross‐sectional characterization (Raman spectroscopy and nanoindentation) was used to examine changes in the mechanical properties and microstructure of two different commercially‐available polyolefins, with similar crystallinities, produced by injection molding—a polypropylene homopolymer (PPH) and a polypropylene random copolymer (PPRC)—aged under accelerated UV‐A conditions. The aim was to characterize the variations in the crystallinity and microstructure across the cross‐section of these materials. Our results suggest that the presence of ethylene comonomer units in PPRC results, on average, in smaller crystal dimensions, leads to improved packing, and a more homogeneous microstructure and hardness across the cross‐section of the sample. The ethylene monomers stabilize PPRC from oxidation during the first 14 days of accelerated aging, but eventually the rate of degradation matches the PPH at 28 days of aging, probably because of the higher surface area to volume ratio of the smaller crystals. The work emphasizes the importance of incorporating ethylene comonomers into polyolefins to limit variation of the microstructure across the core to the skin layer, for improved future design of packaging that degrades fully.

Suppression of Initial Degradation via an Interfacial Charge-Induced Overshooting Effect in Solution-Processed Organic Light-Emitting Diodes.

As the chemical stability of organic materials in organic light-emitting diodes (OLEDs) greatly impacts devices' lifetime, a thoughtful and advanced design of materials and device structures is necessary. In our work, we have achieved lifetime enhancement at its initial stage for solution-processed OLEDs. This improvement was realized through the implementation of a double electron transporting layer (dETL) composed of 2-[4-(9,10-dinaphthalen-2-yl-anthracen-2-yl)-phenyl]-1-phenyl-1H-benzoimidazole (ET) and hydroxyquinolinolato-lithium (Liq). A giant surface potential was generated at the surface of a constituent electron transport layer (ETL) that contained a higher concentration of Liq with high polarity. This giant surface potential simultaneously promoted the injection of trapped/accumulated electrons through the interface within dETL and the injection of holes from the anode, generating more exciton recombination events and ultimately enhancing efficiency by 133.0% and lifetime LT95 (luminance dropped by 5%) by 300% with an overshooting effect. Additionally, the degradation at the emitting layer was mitigated by shifting the degradation zone to the dETL, which was evidenced by laser desorption/ionization-time-of-flight (LDI-TOF) mass spectroscopy.

Predicting fatigue life of multi-defect materials using the fracture mechanics-based physics-informed neural network framework

To address the limitations of traditional methods (such as the S-N curves and Paris’s law) in evaluating the fatigue life of multi-defect materials, this study developed a fracture mechanics-based physics-informed neural network (PINN) to predict the lifetime of multi-defect materials using cyclic loading (Δσ) and the equivalent damage area (AD). Influences of multiple defects were unified characterized through the equivalent damage area, which was calculated based on the M−integral fatigue model. This model reflects the energy evolution of multi-defect fatigue damage. By embedding the prior knowledge of fracture mechanics derived from the M−integral fatigue model into the loss function of PINN, crucial physical information was captured during the training progress, enhancing the interpretability of the neural network. By integrating the advantage of the M−integral fatigue model in characterizing the fatigue performance of multi-defect materials and the nonlinear fitting ability of neural networks, the proposed approach effectively improves the generalization ability and predictive accuracy of limited fatigue data. The presented PINN models accurately forecast the fatigue life of multi-defect materials, with a squared correlation coefficient (R2) exceeding 0.9. The presented methodological framework addresses the existing gap in methods for evaluating the fatigue performance of multi-defect materials and reliance on fatigue testing.

Improving the durability and investing failure behavior of TBCs under thermal cycling-CMAS test by Yb2O3 and Y2O3 co-stabilized ZrO2 materials and different processes

Under extremely complex conditions, extending the lifetime of thermal barrier coatings (TBCs) is a challenge. In the present study, optimization of the coating structure and selection of coating materials are beneficial for improving the lifetime of TBCs under thermal cycling-CMAS (calcium-magnesium-alumina-silicate) test. It is efficient to obtain different layer thicknesses of multi-layer coating, including the micro-nano dual-scale layer, the dense YbYSZ layer (4.0 mol % Yb2O3 and 0.5 mol% Y2O3 co-stabilized ZrO2), the porous YbYSZ layer and the laser 3D texturing layer, using the computational model under thermal load. Based on the corresponding coating structure and YbYSZ material, bond strength and thermal cycling-CMAS lifetime are evaluated, and compared with those of YSZ (4.5 mol % Y2O3 stabilized ZrO2) coating. The results reveal that TBCs with porous embedded particle cluster (PEPC) structure is lower than that of YSZ coating. In addition, the original defects in multi-layer coating with grid texture reduce the bond strength. The lifetime of multi-layer coatings with a punctate texture are significantly improved in the thermal cycling-CMAS test, and their failure behavior includes fragmented and bulk-like exfoliation. This study emphasizes that combination of materials modification and structure optimization are a promising strategy to extend lifetime of TBCs.

Replacement Implant-Retained Ear Prosthesis Using Semi-Digital Workflow: A Case Report.

Defects in the facial region can be treated by maxillofacial prostheses however, fabrication of the prosthesis is a time-consuming process. The short lifetime of silicone material due to inherent deterioration has stimulated a search for more practical methods. This case report involves a semi-digital workflow for replacement of an ear prosthesis. The existing contralateral intact ear and retentive bar of the existing prosthesis were scanned using an intraoral scanner. Resin models of the bar and the mirror image of the ear were fabricated using a 3D printer and wax replicas were obtained using silicone impression material. This method was successful, time-saving, and comfortable for the clinician and patient.

The scattering lifetime and thermoelectric properties for an inorganic flexible material of α-Ag2S

To clarified the influence of the scattering mechanism on thermoelectric properties α-Ag2S, the relationship between the scattering lifetime and transport properties of the inorganic flexible material α-Ag2S are investigated for the first time using first-principles calculation, Boltzmann transport theory, and the momentum relaxation time approximation (MRTA). Calculations reveal that the static dielectric constant, high frequency dielectric constant, and elastic constant are anisotropic. The acoustic deformation potential scattering (ADP), the ionized impurity scattering (IMP), the piezoelectric scattering (PIE), and the polar optical phonon scattering (POP) of α-Ag2S are first calculated, and the IMP and POP are found to be the major contributions for scattering mechanism. Furthermore, it is also found that the transverse wave of α-Ag2S effects on electrons along the XZ shear strain direction are non-negligible. These insights provide a new direction for the regulation of thermoelectric properties in α-Ag2S by offering a deeper understanding of the scattering mechanisms.

Plasma burn-mind the gap.

The programme to design plasma scenarios for the Spherical Tokamak for Energy Production (STEP), a reactor concept aiming at net electricity production, seeks to exploit the inherent advantages of the spherical tokamak (ST) while making conservative assumptions about plasma performance. This approach is motivated by the large gap between present-day STs and future burning plasmas based on this concept. It is concluded that plasma exhaust in such a device is most likely to be manageable in a double null (DN) configuration, and that high core performance is favoured by positive triangularity (PT) plasmas with an elevated central safety factor. Based on a full technical and physics assessment of external heating and current drive (CD) systems, it was decided that the external CD is provided most effectively by microwaves. Operation with active resistive wall mode (RWM) stabilization as well as high elongation is needed for the most compact solution. The gap between existing devices and STEP is most pronounced in the area of core transport, owing to high normalized plasma pressure in the latter which changes qualitatively the nature of the turbulence controlling transport. Plugging this gap will require dedicated experiments, particularly on high-performance STs, and the development of reduced models that faithfully represent turbulent transport at high normalized pressure. Plasma scenarios in STEP will also need to be such that edge localized modes (ELMs) either do not occur or are small enough to be compatible with material lifetime limits. The high current needed for a power plant-relevant plasma leads to the unavoidable generation of high runaway electron beam current during a disruption, where novel mitigation techniques may be needed. This article is part of the theme issue 'Delivering Fusion Energy - The Spherical Tokamak for Energy Production (STEP)'.

Hybrid metal halide family with color-time-dual-resolved phosphorescence for multiplexed information security applications

Luminescent materials with engineered optical properties play an important role in anti-counterfeiting and information security technology. However, conventional luminescent coding is limited by fluorescence color or intensity, and high-level multi-dimensional luminescent encryption technology remains a critically challenging goal in different scenarios. To improve the encoding capacity, we present an optical multiplexing concept by synchronously manipulating the emission color and decay lifetimes of room-temperature phosphorescence materials at molecular level. Herein, we devise a family of zero-dimensional (0D) hybrid metal halides by combining organic phosphonium cations and metal halide tetrahedral anions as independent luminescent centers, which display blue phosphorescence and green persistent afterglow with the highest quantum yields of 39.9 % and 57.3 %, respectively. Significantly, the luminescence lifetime can be fine-tuned in the range of 0.0968–0.5046 μs and 33.46–125.61 ms as temporary time coding through precisely controlling the heavy atomic effect and inter-molecular interactions. As a consequence, synchronous blue phosphorescence and green afterglow are integrated into one 0D halide platform with adjustable emission lifetime acting as color- and time-resolved dual RTP materials, which realize the multiple applications in high-level anti-counterfeiting and information storage. The color-lifetime-dual-resolved encoding ability greatly broadens the scope of luminescent halide materials for optical multiplexing applications.

Dynamic material flow analysis of construction materials in Saudi Arabia: Strategies for sustainability of residential buildings

Globally, the expansion of building infrastructure has serious environmental implications due to emissions from cement and steel. The construction industry uses the vast majority of cement and steel produced globally and locally. Consequently, this paper proposes a model to estimate and mitigate future material flow emissions into residential buildings in Saudi Arabia. First, a dynamic material flow model is used to quantify material flows and stock in residential buildings. The evolution of Saudi housing stock and related steel and cement are simulated from 1950 to 2100. Second, various strategies such as material efficiency improvement, lifetime extension, and reducing production emissions are simulated to reduce emissions caused by cement and steel. The findings indicate that implementing substantial material efficiency improvements can result in 33 %–46 % reductions of cumulative steel and cement emissions from 2023 to 2100, respectively. Furthermore, improving material efficiency measures could result in over 80 % reductions in emissions for steel over the same period. Reducing the ratio of clinker to supplementary cementitious materials in cement to 75 % could reduce cumulative cement emissions by 129 million tCO2e (17 %). Adoption of high material efficiency practices in cement use, low clinker cement, and waste as fuel can reduce emissions by 70 %. The findings of this study contribute to a better understanding of future emissions from building materials used in residential buildings, as well as the impact of emission mitigation strategies on future emissions, which will help decision-makers and researchers develop policies and research.

Enhancing the Room-Temperature Phosphorescence Performance by Salinization of Guests.

Although the host-guest doped strategy effectively improves the phosphorescence performance of materials and greatly enriches the variety of materials, most of the guests are organic molecules with weak luminescence ability, which leads to the need for further improvement in the phosphorescence performance of doped materials. Herein, by salinization of organic molecules, the luminescence performance of the guests was effectively improved, thereby significantly enhancing the phosphorescence performance of the doped system. A compound 4-(naphthalen-2-yl)quinoline (QL) containing nitrogen atom was synthesized as initial guest, then QL was salted to obtain six organic salt guests containing anions BF4-, PF6-, CF3SO3-, N(CF3SO2)2-, ClO4-, and C4F9SO3-, respectively. Two doped systems were constructed using benzophenone and poly(methyl methacrylate) as the hosts. The phosphorescence quantum yield and phosphorescence lifetime of doped materials with QL as guest were only 4.1%/5.2% and 131 ms/141 ms, while those of doped materials with salinized molecules as guests were improved to 32-39% and 534-625 ms, respectively. The single-crystal structures and theoretical calculations indicated that anions can not only enhance the intermolecular interaction of guests but also increase the spin-orbit coupling constant. This work provides an effective strategy for improving the phosphorescence performance of doped materials.

A Highly Sustainable Supramolecular Bioplastic Film with Superior Hydroplasticity and Biodegradability.

Massive accumulation of postconsumer plastic waste in eco-system has raised growing environmental concerns. Sustainable end-of-life managements of the indispensable plastic are highly demanding and challenging in modern society. To relieve the plastic menace, herein we present a full life cycle sustainable supramolecular bioplastic made from biomass-derived polyelectrolyte (chitosan quaternary ammonium salt, QCS) and natural sodium fatty acid (sodium laurate, SL) through solid-phase molecular self-assembly (SPMSA), by which the QCS-SL complexes, precipitated from mixing the aqueous solutions, self-assemble to form bioplastic film by mildly pressing at room temperature. The QCS-SL bioplastic films display superior hydroplasticity owing to the water-activated molecular rearrangement and electrostatic bond reconstruction, which allows facile self-healing and reprocessing at room temperature to significantly extend the service lifetime of both products and raw materials. With higher water content, the dynamic electrostatic interactions and precipitation-dissolution equilibrium endow the QCS-SL bioplastic films with considerable solubility in water, which is promising to mitigate the plastic accumulation in aquatic environment. Because both QCS and SL are biocompatible and biodegradable, the dissolved QCS-SL films are nontoxic and environmentally friendly. Thus, this novel supramolecular bioplastic is highly sustainable throughout the whole life cycle, which is expected to open a new vista in sustainable plastic materials.

Supramolecular J- and H-Aggregation of Naphthalimide-Conjugated Dipeptide in Mixed-Solvent Systems and its Application in Cell Imaging.

In this work, a core-substituted NMI-conjugated dipeptide (4MNLV) was extensively studied in mixed solvent systems to explore the polarity effect on the self-assembly pattern and their photophysical property. 4MNLV adopted J- or H- type aggregation pattern depending upon the polarity index of the solvent system chosen. The self-assembly process was achieved through the anti-solvent effect. UV-vis study suggested that if the stock solution of 4MNLV was diluted with a relatively more polar solvent (compared to the stock solvent), then the system acquired J- type of aggregation pattern by showing a red-shift in their absorption maxima (λmax). Conversely, when the stock was diluted by a relatively less polar solvent, H-type of aggregation was observed, where blue shift of λmax was noticed. The emission spectra and the lifetime of the self-assembled materials were also influenced by the chosen solvent system. The chirotopic behaviour of these self-assembled materials was studied through CD spectroscopy. Morphological study indicated the formation of helical nanofibrillar structures. The bright green fluorescence of these highly biocompatible naphthalimide-peptide conjugate was used for cell imaging application, indicating its futuristic scope.

Numerical analysis of plastic deformation mechanisms in polycrystalline copper under cyclic loading with different frequencies

The frequency of cyclic loading has a strong effect on the fatigue lifetime of materials. High loading frequencies allow reaching very high cycle fatigue regimes. The effects of cyclic loading with different frequencies are studied using the finite element method within the framework of crystal plasticity. The numerical study represents copper polycrystal that undergoes tension–compression loading with frequencies 80 Hz and 20 kHz respectively. The spatial distributions of stresses, strains, and plastic slip are used for estimation of volume fraction, morphology, and plasticity mechanism of persistent slip bands. The results show that at 80 Hz cyclic loading, plasticity in persistent slip band cells is dominated by the creation and annihilation of dislocations while at 20 kHz cyclic loading, plasticity is driven by the back-and-forth movement of dislocations inside the persistent slip band cells. The numerical study shows a correlation between amplitude and frequency of loading with spatial distribution and morphology of persistent slip bands that can be related to the fatigue lifetime.

Non-linear MHD investigations of high-confinement regimes without type-I ELMs in ASDEX Upgrade and JT-60SA

Large edge localised modes (ELMs) would cause an unacceptable reduction of material lifetime in future large tokamaks due to the significant amount of energy expelled from the magnetically confined region towards the plasma facing components. Thoroughly validated modelling of regimes devoid of large ELMs is crucial as it may then provide predictive insights prior to tokamak operation and design. This paper describes recent efforts pursued with the non-linear extended MHD code JOREK in the modelling of three scenarios without large ELMs: quiescent H-mode (QH-mode), quasi-continuous exhaust regime (QCE regime), and the enhanced D-alpha H-mode (EDA H-mode). For each of these regimes, the non-linear dynamics observed in the simulations are detailed and compared to experimental observations of the underlying instabilities of each regime (edge harmonic oscillation for QH-mode, small ELMs for QCE regime, and quasi-coherent mode for EDA H-mode). For QH-mode, the kink-peeling mode is found to govern the dynamics and a transition to a large ELM is obtained above the same density threshold as in the modelled experiment. For the QCE regime and EDA H-mode, resistive peeling–ballooning modes dominate and pedestal fluctuation frequencies correspond well to experimental observations. The dominant mechanisms for the excitation and suppression of these instabilities are presented and their influence on simulation dynamics is shown. Finally, predictive simulations of edge instabilities at different values of plasma resistivity in a 4.60 MA scenario with low edge safety factor in JT-60SA are presented.

Ultrasonic Study of Longitudinal Critically Refracted and Bulk Waves of the Heat-Affected Zone of a Low-Carbon Steel Welded Joint under Fatigue

Currently, ultrasonic methods for assessing the fatigue lifetime of various structural materials are being actively developed. Many steel constructions are made by welding. The weld heat-affected zone is the weak point of the construction, as it is most susceptible to destruction. Therefore, it is actually important to search for acoustic parameters that uniquely characterize the structural damage accumulation in the heat-affected zone of a welded joint in order to predict failure. In this work, the specimens were made from the base metal and the welded joint’s heat-affected zone. The specimens were subjected to uniaxial tension–compression under a symmetrical cycle in the region of low-cycle fatigue with control of the strain amplitude. The propagation bulk velocities of longitudinal, shear waves and subsurface longitudinal critically refracted (LCR) waves during cyclic loading were studied. The acoustic birefringence of shear waves was calculated, and a similar parameter was proposed for longitudinal and LCR waves. The dependence of the elastic modulus ratio on the cycle ratio was obtained. It was shown that the acoustic parameters change most intensively in the heat-affected zone. According to the data of the C33/C55 ratio changes measured through the ultrasonic method, a formula for calculating the remaining fatigue life in the heat-affected zone was proposed.