Lamellar Thickness Research Articles

Solution Strengthening and Short-Range Order in Cold-Drawn Pearlitic Steel Wires

Pearlitic steel rods are subjected to cold-drawing processes to produce pearlitic steel wires with true strains ranging from 0.81 to 2.18. Tensile tests are utilized to attain mechanical properties of cold-drawn pearlitic steel wires. TEM and XRD investigations were performed on the microstructure of the cold-drawn steel wires. With an increasing cold-drawn strain, both the interlamellar spacing and cementite lamellae thickness decrease, while the dislocation density significantly increases. The drawn wire has a tensile strength of 2170 MPa when the true stain reaches 2.18. Deformation-induced cementite dissolution occurs during cold-drawing progress, which releases many C atoms. The findings indicate that the supersaturation of C is heterogeneously distributed in the ferrite matrix. The ordered distribution of the released C in ferrite phases creates short-range order (SRO). SRO clusters and disordered Cottrell atmospheres contribute to solution strengthening, which, together with dislocation strengthening and interlamellar boundary strengthening, form an effective strengthening mechanism in cold-drawn pearlitic steel wires. Our work provides new insights into carbon redistribution and the mechanism of solution strengthening within ferrous phases.

Quantitative Analysis of TPU Microstructure and Performance Optimization across Various Processing Conditions.

Thermoplastic polyurethane (TPU) is essential in resource exploration, healthcare, automotive, and high-end recreational sports. Despite extensive research on TPU's microstructures and their macroscopic properties, the impact of processing conditions like compression and injection molding remains underexplored. This study investigates the influence of processing conditions on TPU by preparing samples with varying hard segment contents using compression molding at 205 °C and injection molding at melt temperatures of 205, 210, 215, and 220 °C, followed by heat treatment at 120 °C for 12 h. Results indicate that injection-molded TPU at 205 °C exhibits lower hydrogen bonding, crystallinity, long period, interfacial thickness, and lamella thickness than compression-molded TPU, leading to higher Young's modulus but lower elongation at break. As melt temperatures increase, these microstructural parameters decrease, reducing Young's modulus and increasing elongation at break. Post heat treatment, microstructural parameters increase, aligning Young's modulus with that of compression-molded samples, while elongation at break surpasses them. This suggests that heat treatment enhances microphase separation by rearranging hard and soft segments. our research reveals a consistent pattern across TPUs with varying hard segment contents, indicating that adjusting processing parameters can effectively regulate microstructure and performance, offering valuable insights for developing high-performance polyurethanes.

Plastic strain localization in Bouligand structures

The Bouligand structure represents helicoidal stacking of aligned fibers; such a structure is widely observed in biological composites. Despite the progress in characterization of toughening caused by Bouligand arrangement of fibers, the inelastic deformation mechanisms of this structure remain elusive. In this study, we carry out calculations for plastic deformation of Bouligand structure, crossed-lamellar structure and the single lamellar structure. It is found that the single lamellar structure and crossed-lamellar structure can undergo necking, while in the Bouligand structure, plastic strain localization bands develop, which is accompanied by plastic rotating of fibers, lamellar twisting and lamellar delamination. Compared with crossed-lamellar structure, the Bouligand structure exhibits lower plastic energy dissipation. However, the Bouligand pattern can activate delamination of lamellae, generating high level of damage energy dissipation. The plastic deformation of Bouligand structure depends on the fracture properties of interface between adjacent lamellae. It is identified that the plastic dissipation of Bouligand structure increases with increasing cohesive strength of lamellar interface, and dominant shear bands emerge in the case of weak lamellar interface. The high strength of lamellar interface plays a role in promoting twisting of lamellae. We have further revealed the effect of the thickness of individual lamella on plastic deformation of the Bouligand structure. The thick lamella is capable of suppressing plastic strain localization in Bouligand structure, thereby giving rise to high plastic dissipation. The findings of this study shed new light on the development of bioinspired Bouligand-type materials.

Direct numerical simulation of coalescence and separation of binary droplet collision with lamella stabilization

Binary droplet collision is a fundamental aspect of various natural phenomena and industrial applications. In this work, direct numerical simulation of coalescence and separation of binary droplet collision is performed over a wide range of Weber numbers and impact factors. The incompressible Navier–Stokes equations are solved by the finite volume approach, coupled with the volume of fluid method. To address the inaccurate prediction of thin lamella in simulation, a lamella stabilization method is introduced to resolve the lamella by adjusting the grid resolution. Compared with experimental data, it is validated that the lamella can be accurately and fully captured with this lamella stabilization method. Moreover, the analysis of shape and energy during the collision is conducted, and the variation of lamella is described in detail, particularly the evolution of the thickness of lamella. The results suggest that for obtaining the full variation of lamella, the maximum refinement size of the grid can reach D/4096. It is also found that without lamella stabilization, excessive dissipation can lead to the failure of predicting coalescence and separation, especially for the cases in the transition between coalescence and separation. Furthermore, even if the same collision outcome can be obtained without lamella stabilization, the number and size of droplets have obvious differences.

Micro-structure-property relationship of heavily drawn steel wires for large span suspension bridge cables

The outstanding combination of high strength and ductility of bridge cable steel wire is attributed to the cold drawing process with intermediate equivalent strain. However, the micro-structure-property relationship of heavily drawn steel wires for large span suspension bridge cables is not well understood. In this study, defects-controlled deformation in nano-scale interfaces between ferrite and cementite phases with heavily cold drawing process was investigated using high-resolution transmission electron microscopy and molecular dynamics simulation. The excessive thinning of the cementite lamellar thickness observed from the morphology suggested the evolution of the Fe3C/Fe interface in the cold-drawn wires, namely, the partial cementite deformation during the drawing process. Drawing strain played a major role in the occurrence of partial cementite nano-crystallisation. This was because the change in cementite morphology was the primary cause of cementite free energy increase, which ultimately led to cementite phase instability. The decrease of yield strength during the drawing process of the bridge cable steel wire was caused by the inverse Hall-Petch effect resulted from the nodule rotation. When the nodule morphology became flat, the inverse Hall-Petch effect was suppressed. At this time, the strengthening mechanism caused by cementite nano-crystallisation ensured the improvement of tensile strength of steel wire when the dislocation density was close to saturation.

Supramolecular structure and in vitro digestive properties of plasma-treated corn starches varying in amylose content

The effects of plasma treatment on the multi-scale structure and in vitro digestibility of maize starch with different amylose contents were systematically evaluated. The results demonstrated that all maize starches' molecular weights (MW) decreased when treated with plasma, among which the MW of waxy maize starch displayed the largest reduction. Plasma treatment led to an increase in the thickness of the semi-crystalline lamellae and double helix proportions of waxy and normal maize starches. However, high-amylose maize starch presented a less ordered structure by plasma treatment. Additionally, larger pores and channels were observed on the surface of plasma-treated waxy and normal maize starch granules. Moreover, deposits were displayed on the surface of high-amylose maize starch granules. These changes increased the in vitro digestibility and hydrolysis rate of three starches after plasma treatment. Notably, plasma treatment caused diverse alterations in the structure and functionality of maize starch varying in amylose content, leading to maize starch with better digestibility, therefore being used as an ingredient for functional foods.

The multi-scale structure and in vitro digestive kinetics of underutilized Chinese seedless breadfruit starch

In our previous research, the significant difference of physiochemistry properties for underutilized starches was showed between Chinese seedless breadfruit species and the other species. Based on this, the multiscale structure and digestion kinetics of Chinese seedless breadfruit of Spice and Beverage Research Institute species (SBS) and Xinglong species (XBS) was further researched. The SBS exhibited higher α-1,6 glycosylic bond content, free side-chain groups content, double-helix content, homogeneity, molecular weight, and V-type polymorphism, and fewer amorphous content, blocklet sizes, and a smaller semi-crystalline lamella thickness than XBS. Additionally, SBS showed higher final viscosity, pasting temperature, and gelatinization enthalpy than those of XBS. Consequently, SBS display lower rate constant (0.73 h−1) and glycemic index (65.17) than those of XBS (0.86 h−1 and 73.95). The anti-digestibility mechanism was revealed by the structure-digestibility relationship. It was found that resistant starch of SBS and XBS were significantly higher than those of starch from American and African species. This indicated that Chinese breadfruit starch could be considered as a good source of resistant starch, regulating glycemic index. In summary, XBS and XBS could be considered as a well source of resistant starch to make foods for preventing or improving type II diabetes or hyperlipemia.

Microstructure and strength of cold-drawn large strain Fe35Ni35Cr20Mn10 high-entropy alloy

The Fe35Ni35Cr20Mn10 high-entropy alloy wires can achieve a large strain of 8.73 and a section reduction ratio of 99.98 %,and possess a high strength of 1868 MPa via traditional wire drawing. The microstructure evolution and mechanical properties of cold-drawn Fe35Ni35Cr20Mn10 high-entropy alloy are characterized by microstructure observation and tensile test. The results showed that The Fe35Ni35Cr20Mn10 HEA has excellent plastic forming capacity and excellent phase stability during plastic deformation. The Fe35Ni35Cr20Mn10 HEA has excellent continuous drawing ability, the main deformation mechanism is the plane slip and cross slip of the dislocation and the dynamic recovery of the sublamellar layer make the lamellar structure maintain a dynamic equilibrium state, and the lamellar thickness is basically unchanged to support the continuous plastic deformation under high strain conditions. The dynamic balance of coarsening and refining of lamellar structure in the process of plastic deformation is mainly due to the merging of HEA lamellar caused by the movement of trigeminal node induced by strain. Texture evolution showed that the <111> and <100> fiber textures were the stable texture component and the texture component content remained unchanged even under further increased strain. The Fe35Ni35Cr20Mn10 high-entropy alloy wire with high strain of 8.73 possesses excellent strength, and its tensile strength is 1868 MPa at room temperature, which has the largest strain. The dislocations proliferation, lamellar structure refinement and texture strengthening lead to high strength of the Fe35Ni35Cr20Mn10 high-entropy alloy wire.

The effects of UV aging process on the structure and properties of high-tenacity poly(ethylene terephthalate) industrial fiber

The high-tenacity poly(ethylene terephthalate) (HT PET) industrial fibers (1100 dtex/ 192f) were fixed in position with a constant fiber length and subjected to accelerated artificial ultraviolet exposure with temperature of 50 °C to assess their degradation mechanism. The structural evolutions were evaluated using a combination of ex-situ wide-angle X-ray diffraction (WAXD), ex-situ small angle X-ray scattering (SAXS), Fourier transform infrared spectroscopy (FTIR), and intrinsic viscosity tests based on the relaxed aged samples after different aging process. The results indicate that the structures and properties evolutions of HT PET industrial fiber under UV aging process can be categorized into three stages. In the pre-aging stage (t ≤ 0.5d), the fiber experiences a slight decline in tenacity and thermal shrinkage properties due to the combined impact of UV radiation and heat treatment. Subsequently, in the mid-aging stage (0.5d < t ≤ 28d), a notable decrease in the fiber's elongation at break is observed, accompanied by visible macroscopic defects arising from photo-oxidative aging on the fiber surface after 16 days of exposure. While the fiber's unit cell and atomic positions remains stable on atomic scale, the lamellar thickness and long period witness a significant reduction owing to high-orientation molecular breakages in the mesophase region. Moreover, rearrangement of molecular chains leads to a reduction in the tilting angle. In the late-aging stage (t > 28d), the degradation rate of mechanical and thermal shrinkage properties of the fiber decelerates, alongside a decline in intrinsic viscosity. These results suggest that the fiber's crystallinity remains unchanged post UV aging, with the deterioration in mechanical properties of HT PET industrial fiber primarily attributed to molecular degradation during UV exposure.

Feasibility of Using Polymers to Improve Foam Flow Performance in Vertical Pipes: Application to Liquid Unloading in Gas Wells

Foam unloading is a cost-effective technique for removing liquid from low-energy gas wells, but it faces challenges due to the instability of foam at the wellbore. Surfactants alone struggle to create and maintain durable foam films under wellbore conditions. Polymers are known to enhance foam stability by increasing lamella thickness and viscosity, but their impact on foam unloading has not been well explored. This study investigates the effects of Xanthan Gum (XG) and Polyvinylpyrrolidone (PVP) polymers on stability and unloading efficiency of the foams made by Alkyl Polyglycoside surfactant. The research evaluates foam stability and examines the bubble size and lamella thickness under varying salinity conditions. Additionally, the study evaluates foam unloading efficiency by determining unloaded mass rate, critical gas velocity and Weber number. Results show that polymer concentration, type and molecular weight significantly affect foam morphology and stability. Xanthan Gum at 1000 ppm demonstrated the smallest bubble size and greatest foam stability. This concentration also achieved the highest unloaded mass, 30% more than the surfactant-only case. Regarding the molecular weight of the polymers, HPVP demonstrated an ability to generate smaller bubbles in comparison with LPVP. Consequently, HPVP exhibited superior performance in liquid unloading, surpassing LPVP by a margin of 8.5%. The addition of polymers reduced critical gas velocity, with 1000 ppm of XG yielding the lowest value. Initially, the Weber numbers for polymer-stabilised foams were higher than the surfactant-only case (XG: 208.01, LPVP: 17.70, HPVP: 26.38 vs. APG: 2.25) due to the Marangoni effect but decreased during the unloading process (XG: 788.58, LPVP: 1850.26, HPVP: 1702.01 vs. base case: 4046.42), indicating improved stability and performance. Overall, the study demonstrates that polymers can significantly improve foam stability and performance, maintaining foam integrity throughout the unloading process if engineered properly prior to their application.

The potassium storage performance of carbon nanosheets derived from heavy oils

As by-products of petroleum refining, heavy oils are characterized by a high carbon content, low cost and great variability, making them competitive precursors for the anodes of potassium ion batteries (PIBs). However, the relationship between heavy oil composition and potassium storage performance remains unclear. Using heavy oils containing distinct chemical groups as the carbon source, namely fluid catalytic cracking slurry (FCCS), petroleum asphalt (PA) and deoiled asphalt (DOA), three carbon nanosheets (CNS) were prepared through a molten salt method, and used as the anodes for PIBs. The composition of the heavy oil determines the lamellar thicknesses, sp3-C/sp2-C ratio and defect concentration, thereby affecting the potassium storage performance. The high content of aromatic hydrocarbons and moderate amount of heavy component moieties in FCCS produce carbon nanosheets (CNS-FCCS) that have a smaller layer thickness, larger interlayer spacing (0.372 nm), and increased number of folds than in CNS derived from the other three precursors. These features give it faster charge/ion transfer, more potassium storage sites and better reaction kinetics. CNS-FCCS has a remarkable K+ storage capacity (248.7 mAh g−1 after 100 cycles at 0.1 A g−1), long cycle lifespan (190.8 mAh g−1 after 800 cycles at 1.0 A g−1) and excellent rate capability, ranking it among the best materials for this application. This work sheds light on the influence of heavy oil composition on carbon structure and electrochemical performance, and provides guidance for the design and development of advanced heavy oil-derived carbon electrodes for PIBs.

Heterogeneous microstructure of γ-irradiated pre-oxidized PAN fiber revealed by microfocus SR-SAXS reconstruction and molecular simulation.

The microstructure plays a crucial role in the manufacturing and application of polyacrylonitrile fibers, which serve as precursors for carbon fibers. Synchrotron radiation small angle x-ray scattering (SR-SAXS) is a non-destructive and precise technique for analyzing fiber structures. This study employed one-dimensional SR-SAXS mapping to extract key structural parameters such as periodicity, lamellae thickness, and the extent of amorphous regions, as well as the directional orientation in γ-irradiated, pre-oxidized polyacrylonitrile fibers. The analysis revealed a three-layered structure comprising a surface skin, a transitional layer, and a central core. Notably, the lamellar thickness exhibits a "U"-shaped distribution, while the long-period structures, amorphous regions, and orientational properties demonstrate a "wave-like" pattern. Within this structure, the skin exhibits a higher level of orientation, with the orientation decreasing progressively from the skin toward the core layer. The structure of the layered crystal was further corroborated by the morphological analysis. In addition, molecular simulations were performed to propose the mechanisms underlying the formation of this layered structure. This comprehensive investigation using SR-SAXS and one-dimensional mapping provides detailed insights into the microstructural and morphological characteristics of polyacrylonitrile fibers, which can inform future advancements in material processing and refinement techniques for the production of advanced fibers.

Mechanistic understanding of changes in physicochemical properties of different rice starches under high hydrostatic pressure treatment based on molecular and supramolecular structures

The molecular and supramolecular structures of japonica and waxy rice starches under high hydrostatic pressure treatment (450 MPa) were studied and the changes in physicochemical properties were analyzed based on these structures. The molecular structures of japonica and waxy rice starch cause differences in the lamellar structure and physicochemical properties. The thickness of amorphous lamella of japonica rice starch increased at 5 min (2.95 nm) followed by a gradual collapse of lamellar structure. Whereas the thickness of crystalline lamellae of waxy rice starch increased at 15 min (5.92 nm) and the lamellae collapsed suddenly at 20 min. The pasting, rheological and textural characteristics of both starches increased significantly within 10 to 15 min. The decreasing onset temperature and enthalpy of high hydrostatic pressure-treated starches indicated easier gelatinization. High hydrostatic pressure-treatment offers potential for developing starch-based products with low swelling capacity, easy gelatinization, high viscosity and hardness.

Thermal stability of a newly developed Mn containing β-solidifying γ-TiAl intermetallic compound at 750 °C

A newly low-cost β-solidifying γ-TiAl alloy Ti-44Al-3Mn-0.4Mo-0.4W-0.1B-0.1C (in at. %, named as TMMW) was invented. The rolled bars with a diameter of 12 mm were successfully fabricated by conventional hot rolling process, directly carrying out from the ingot without the pre-forging or hot-packing. The heat-treated TMMW rolled bar, which had a fine-grained nearly lamellar (NL) microstructure, was then air-exposed at 750 °C for up to 3000 h. The changes of the microstructure during this exposure were characterized using electron probe X-ray micro-analyzer (EPMA), transmission electron microscope (TEM), electron backscattered diffraction (EBSD) and high-energy X-ray diffraction (HEXRD). The tensile properties of the samples before and after thermal exposure were also tested. The fine-grained NL microstructure is found to be thermodynamically stable during the exposure. Meanwhile, the combined addition of Mo and W shows a positive effect on the stabilization of βo phase at colony boundaries, with only slight precipitation of the nanometer βo phases with no other brittle phases, such as Laves, in the metastable α2 lamellae. It is found that the thickness of the α2 lamellae decreases after 500 h exposure, while remains basically unchanged from 500 h to 3000 h, which is contributed by the effective pinning effect of the precipitated βo phase in α2 lamellae. As a result, the exposure-induced embrittlement under room temperature and elevated temperature does not take place. Interestingly, the ductility tested at 800 °C improves significantly after exposure. As for the tensile strength, it is only reduced by less than 10 % after 500 h exposure, while it remains essentially unchanged when increasing the exposure time from 500 h to 3000 h. Finally, the mechanisms of the precipitation of βo phases in the α2 lamellae and the tensile properties evolution during the exposure were carefully discussed.

Simultaneous Measurement of Two-Trace Two-Dimensional (2T2D) Near-Infrared (NIR) Asynchronous Correlation Spectra and Small-Angle X-ray Scattering (SAXS) to Characterize Thermally Aged Polypropylene (PP).

In this study, a new system was developed to carry out simultaneous near-infrared (NIR) and small-angle X-ray scattering (SAXS) measurements. Aged polypropylene (PP) was examined with the NIR-SAXS system to demonstrate how it can be utilized to derive pertinent information about the polymer structure. Pairs of SAXS profiles and NIR spectra of PP in its initial state and after aging were measured to derive an in-depth understanding of the aging phenomenon. The SAXS profiles of the PP samples showed a clear shift of the SAXS peak to the lower q direction induced by the thermal aging, indicating an increase in the length of the long-period structure. Two-trace two-dimensional (2T2D) asynchronous correlation spectra derived from NIR spectra clearly revealed that the aging treatment leads to a substantial increase in the spectral intensity of the regularity bands representing the longer helix present in a folded lamellar structure. In other words, it suggests that the long helix structure is more abundantly present than the short helix structure in the aged PP than in the initial PP. By combining the information derived from the SAXS profiles and NIR spectra, the details of the aging-induced variation were clearly determined. Namely, aging causes additional crystallization of the PP by developing more helical structures, which involves an increase in the lamellar thickness as well as a decrease in the amorphous region. The growth of the rigid crystalline phase restricts the elastic deformation in the amorphous structure, which eventually induces the deterioration of PP by making the polymer hard but brittle. Such observation, in turn, implies that retarding or accelerating the crystallized structure of PP substantially works to control the progress of aging.

Successive self-nucleation and Annealing technique applied to polypropylene/butyl rubber composites: Recycling alternatives for vacuum bagging materials

The aerospace sector uses butyl rubber to manufacture carbon fiber components through an autoclave or infusion. Both manufacturing techniques require a high vacuum to achieve adequate impregnation of the carbon fiber fabrics with epoxy resin, and butyl rubber is used as the sealant. The aerospace sector discontinues materials with shelf life expired, and butyl rubber is one of the materials most discontinued for not being used within the designated time. This work presents the development of composites using polypropylene and discontinued butyl tape. Composites with 30, 50, and 70 wt% of butyl rubber content were prepared using a twin-screw extruder. The structural analysis showed that the composites with 50 wt% and 70 wt% are similar to butyl rubber, while the compound with 30 wt% of butyl is similar to polypropylene. The degree of crystallinity of the compound with 50 wt% of butyl content was 18% higher than the PP, and the melting temperature decreased by 30% with the higher butyl content. SSA revealed that the highest enthalpic contribution occurred in the crystalline fraction of higher perfection, except for the compound with 50 wt% of butyl content, whose less perfect crystalline populations grew at the expense of the most perfect crystals. The reduction of the crystalline fraction implies that butyl interferes with the formation of crystals, developing populations with lower lamellar thickness that favors the overall crystallinity of the compound. Young’s modulus, yield strength, and nominal strain decreased with butyl rubber content. The composites showed rough failure surfaces with solid butyl rubber particles and poor adhesion to polypropylene. Butyl particles with diverse sizes and geometries lead to sudden failure of the composites and high dispersion in strain values.

Investigation of starch hierarchical structure in relation to physicochemical properties and digestive behavior under different high hydrostatic pressure treatment time

Changes and causal relationships in the hierarchical structure, thermal, pasting and rheological properties, as well as the digestive behavior of starch under different high hydrostatic pressure (HHP) treatment time were investigated. At 5 min, the thickness of amorphous lamellae increased (2.76 nm) and the content of B2 and B3 chains in the amorphous lamellae decreased significantly (10.78 % and 9.08 %). As the treatment time increased, the crystalline lamellae swelled and tightly arranged double helices located in the crystalline lamellae were disturbed, resulting in a decrease in the content of double helices (12.16 %) and relative crystallinity (16.96 %). Helix dissociation, crystal disruption, lamellar collapse and granule deformation were observed at 20 min. These structural changes were closely linked to variations in the physicochemical behaviors. The thermal parameters decreased gradually, accompanied by a decrease in double helix stability. The swollen crystalline lamellae provided more space for molecular stretching, thus enhancing the pasting characteristics. Regarding the digestive behavior, the swollen amorphous lamellae facilitated the invention of enzyme molecules to hydrolyze the starch at 5 min. The digestion rate coefficient and rapidly digestible starch content increased significantly until 15 min, which demonstrated that starch was more easily digested while retaining its intact granular form.

Long-term thermal acclimation enhances heat resistance of Hong Kong catfish (Clarias fuscus) by modulating gill tissue structure, antioxidant capacity and immune metabolic pathways

The rapid temperature changes caused by global warming significantly challenge fish survival by affecting various biological processes. Fish generally mitigate stress through physiological plasticity, but when temperature changes exceed their tolerance limits, even adaptable species like Siluriformes can experience internal disruptions. This study investigates the effects of extreme thermal climate on Hong Kong catfish (Clarias fuscus), native to tropical and subtropical regions. C. fuscus were exposed to normal temperature (NT, 26 ℃) or high temperature (HT, 34 ℃) condition for 90 days. Subsequently, histological, biochemical, and transcriptomic changes in gill tissue were observed after exposure to acute high temperatures (34 ℃) and subsequent temperature recovery (26 ℃). Histological analysis revealed that C. fuscus in the HT group exhibited less impact from sudden temperature shifts compared to the NT group, as they adapted by reducing the interlamellar cell mass (ILCM) and lamellae thickness (LT) of gill tissue, thereby mitigating the aftermath of acute heat shock. Biochemical analysis showed that catalase (CAT) activity in the high temperature group continued to increase, while malondialdehyde (MDA) levels decreased, suggesting establishment of a new oxidative balance and enhanced environmental adaptability. Transcriptome analysis identified 520 and 463 differentially expressed genes in the NT and HT groups, respectively, in response to acute temperature changes. Enrichment analysis highlighted that in response to acute temperature changes, the NT group inhibited apoptosis and ferroptosis by regulating the activity of alox12, gclc, and hmox1a, thereby attenuating the adverse effects of heat stress. Conversely, the HT group increased the activity of pfkma and pkma to provide sufficient energy for tissue repair. The higher degree of heat shock protein (Hsp) response in NT group also indicated more severe heat stress injury. These findings demonstrate alterations in gill tissue structure, regulation of oxidative balance, and the response of immune metabolic pathways to acute temperature fluctuations in C. fuscus following thermal exposure, suggesting potential avenues for further exploration into the thermal tolerance plasticity of fish adapting to global warming.

Effect of the crystal orientation on the enzymatic degradation rate of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH) fibers

In this study, the relationship between the crystal orientation and enzymatic degradation rate of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH) was investigated. The enzymatic degradation rates of melt-spun PHBH fibers were quantified via PHB depolymerase from Ralstonia pickettii T1, and the degradation rate decreased with increasing drawing ratio. The solid structure was investigated via differential scanning calorimetry and small-angle X-ray scattering, and kinetic analysis was performed, indicating that the degradation rate was affected not only by crystallinity and lamellar thickness but also by highly ordered structure. The highly ordered structure was examined via wide-angle X-ray diffraction. The enzymatic degradation rate from the fiber cross-sections was then quantified for the first time, and it increased with drawing ratio and was larger than that from the fiber sides. This result showed that the degradation rate varied depending on the crystal orientation. Furthermore, an enzymatic degradation test of PHBH ring-banded spherulites was conducted, and it was found that the degradation rate of flat-on lamellar crystals was greater than that of edge-on lamellar crystals. This is the first study to quantitatively evaluate the relationship between the crystal orientation and the enzymatic degradation rate.

Strain-rate and size dependence of gradient lamellar nickel investigated by in-situ micropillar compression

Strain rate plays a nonnegligible role in the plastic deformation behavior of metallic materials with heterogeneous nanostructure, while little research focuses on the topic. In-situ compression tests at various strain rates were conducted on the micropillars located at different depths from the gradient lamellar Ni. These tests intended to reveal the strain-rate dependence of micropillars with different lamellar thicknesses and illustrated the competitive relationship between strain rate and intrinsic grain size on the plastic deformation behavior of metallic materials. In addition, due to the strain rate sensitivity related to not only intrinsic size but also external size, single Ni micropillars with different diameters were also compressed at various strain rates in order to clarify the competitive relationship between intrinsic size and external size on the strain rate sensitivity. It is found that lamellar thickness rather than strain rate has more effect on plastic deformation, and external size exhibits a more obvious impact on the strain rate sensitivity. The plastic deformation behaviors of different micropillars are mainly explained by transitions in the effect of lamellar grain boundaries on the dislocation motion at various strain rates and over different lamellar thicknesses, resulting in the change of dislocation multiplication and annihilation rate.