Degradation Mechanism Research Articles

Numerical Investigation of Critical Current and Magnetization Loss Effect for Twisted Stacked Tape Cable Considering Field-Angle Dependency and Mechanical Torsion Degradation

Numerical Investigation of Critical Current and Magnetization Loss Effect for Twisted Stacked Tape Cable Considering Field-Angle Dependency and Mechanical Torsion Degradation

Enhancing mechanical properties, degradation rate, and water resistance of bioplastic Lignin/Polyvinyl Alcohol (PVA) by fractionation of lignin

Enhancing mechanical properties, degradation rate, and water resistance of bioplastic Lignin/Polyvinyl Alcohol (PVA) by fractionation of lignin

Cobalt-Modified Biochar from Rape Straw as Persulfate Activator for Degradation of Antibiotic Metronidazole

A cobalt-loaded magnetic biochar (Co-MBC) catalyst was synthesized to enhance the removal of metronidazole (MNZ). Study explored the performance and mechanism of MNZ degradation by Co-MBC activated permonosulfate (PMS). Results showed that cobalt oxides were effectively deposited onto the biochar surface, new oxygen functional groups were added to the modified biochar, and the presence of the metallic element Co enhanced the efficiency of PMS activation in the composite. More than 90% of MNZ was removed after 60 min with a catalyst dosage of 0.2 g/L and a PS concentration of 1 mM. After four reuses, Co-MBC still showed excellent catalytic performance to degrade over 75% of MNZ. The reaction system performed well even in the presence of inorganic anions and organic macromolecules. However, the degradation rate was inhibited under alkaline conditions. The quenching experiment indicated that •SO4−, •OH, 1O2, and •O2− synergistically degraded MNZ, and that•SO4− played a dominant role. LC-MS was applied to assess intermediate degradation products, in which CO2, H2O, and NO3− were the final degradation products, and potential degradation pathways were suggested. In conclusion, Co-MBC was an efficient and stable catalytic material, and its ability to activate PMS was improved to effectively degrade antibiotics, a typical priority pollutant.

Preparation and Structural-Thermodynamical Investigation of Renewable Copolyesters Based on Poly (Ethylene Succinate) and Polyisosorbide

A series of novel renewable copolymers based on poly(ethylene succinate) (PESu) and poly(isosorbide succinate) (PISSu), with the Isosorbide (Is)/PESu molar ratio varying from 5/95 to 75/25, were synthesized in-situ and studied in this work. A sum of characterization techniques was employed here for the structural and thermo-dynamical characterization. The sophisticated technique of dielectric spectroscopy, along with proper analysis, enabled the molecular dynamics mapping of both the local and segmental types, which is presented for such materials for the first time. With increasing the Is fraction, shorter copolymeric entities were gradually formed. Based on the overall findings, the systems were found to be homogeneous, e.g., exhibiting single glass transitions, with the two polymer segments being found to be excellently distributed. The latter is indirect, although strong, evidence for the successful copolymerization. The thermal degradation mechanism for the copolymers was exhaustingly explored employing analytical pyrolysis. The systems exhibited, in general, good thermal stability, according to the thermogravimetric analysis. Confirming one of the initial scopes for the present systems, isosorbide plays here the role of hardener (PISSu) over the soft polymer (PESu), and this is reflected in the monotonic increase of the glass transition temperature, Tg, from −16 to ~56 °C. The introduction of Is results in an increase in constraints (hardening of the matrix), while there seems to be an overall densification of the polymer (decrease of the free volume).

Reduction performance and degradation mechanism of chlorinated hydrocarbon electrocatalytic hydrodechlorination using synthetic Ti/Pd cathode

In this research, an orthogonal experiment (45) was conducted to explore the degradation of CT in Ti/Pd sealed cathode chamber, and electrochemical characteristics of electrodes were analyzed simultaneously, demonstrating its superior capability for the dechlorination of aqueous CT. The results showed there existed a suitable electrolytic condition for CT hydrodechlorination, when Na2SO4 concentration was 0.4 mg·L−1, current density was 12 mA·cm−2 and initial pH was 7 within 45 min electrolysis time, the 89.42 % of CT was degraded, and the complete vanishment of CT until 65 min occurred. SEM and EDS analysis were used to comprehensively characterize the Ti/Pd cathode. Besides, theoretical calculations showed that Pd modified cathode possesses excellent intrinsic catalytic activity. CV curves and K-L calculation elucidated the one-electron-transfer process underlying the stepwise dechlorination of chlorinated alkanes at the Ti/Pd electrode. Cl− index calculations verified that CT degradation was partial dechlorination. The scavenging activity test of atomic hydrogen (H⁎ads) proved the pivotal roles of H⁎ads in CT hydrodechlorination. The voltage control degradation pathway of CT was put forward, which aligned well with the kinetic model. Overall, the Ti/Pd cathode represents a promising electrode material with significant potential for CT degradation from aqueous solutions.

Enhanced Structure/Interfacial Properties of Single‐Crystal Ni‐Rich LiNi0.92Co0.04Mn0.04O2 Cathodes Synthesized Via LiCl‐NaCl Molten‐Salt Method

Arising from the increasing demand for electric vehicles (EVs), Ni‐rich LiNixCoyMnzO2 (NCM, x + y + z = 1, x ≥ 0.8) cathode with greatly increased energy density are being researched and commercialized for lithium‐ion batteries (LIBs). However, parasitic crack formation during the discharge–charge cycling process remains as a major degradation mechanism. Cracking leads to increase in the specific surface area, loss of electrical contact between the primary particles, and facilitates liquid electrolyte infiltration into the cathode active material, accelerating capacity fading and decrease in lifetime. In contrast, Ni‐rich NCM when used as a single crystal exhibits superior cycling performances due to its rigid mechanical property that resists cracking during long charge–discharge process even under harsh conditions. In this paper, we present comparative investigation between single crystal Ni‐rich LiNi0.92Co0.04Mn0.04O2 (SC) and polycrystalline Ni‐rich LiNi0.92Co0.04Mn0.04O2 (PC). The relatively improved cycling performances of SC are attributed to smaller anisotropic volume change, higher reversibility of phase transition, and resistance to crack formation. The superior properties of SC are demonstrated by in situ characterization and battery tests. Consequently, it is inferred from the results obtained that optimization of preparation conditions can be regarded as a key approach to obtain well crystallized and superior electrochemical performances.

In-Situ Characterization of Cathode Catalyst Degradation in PEM Fuel Cells

The composition and morphology of the cathode catalyst layer (CCL) have a significant impact on the performance and stability of polymer electrolyte membrane fuel cells (PEMFC). Understanding the primary degradation mechanism of the CCL and its influencing factors is crucial for optimizing PEMFC performance and durability. Within this work, we present comprehensive in-situ characterization data focused on cathode catalyst degradation. The dataset consists of 36 unique durability tests with over 4000 testing hours, including variations in the cathode ionomer to carbon ratio, platinum on carbon ratio, ionomer equivalent weight, and carbon support type. The applied accelerated stress tests were conducted with different upper potential limits and relative humidities. Characterization techniques including IV-curves, limiting current measurements, electrochemical impedance spectroscopy, and cyclic voltammetry were employed to analyse changes in performance, charge and mass transfer, and electrochemically active surface area of the catalyst. The aim of the dataset is to improve the understanding of catalyst degradation by allowing comparisons across material variations and provide practical information for other researchers in the field.

The transient thermal ageing of Eurofer 97 by mitigated plasma disruptions

Plasma disruptions in a commercial-scale tokamak will impose high magnitude, short-duration thermal loads on its plasma-facing first wall. Despite a plethora of mitigation measures, these severe, off-normal events are likely to briefly expose the structural materials of the first wall to significant temperature excursions. Eurofer 97, the reference structural material for the plasma-facing first wall of the EU DEMO tokamak, is a reduced activation 9Cr steel with a normalised and tempered ferritic/martensitic microstructure. Repeated exposure to the thermal effects of disruptions over the operating lifetime of a reactor may promote a cumulative evolution of Eurofer 97′s microstructure, affecting key material properties crucial to first wall performance. This novel transient thermal degradation mechanism has been explored via a laser-based transient heating experiment, supported by time-dependent finite element thermal analysis studies of DEMO’s water-cooled lithium–lead first wall during a mitigated plasma disruption. Transient-affected samples of Eurofer 97 were characterised via scanning and transmission electron microscopy techniques (SEM/TEM), including electron backscatter diffraction (EBSD), energy-dispersive X-ray spectroscopy (EDX), and selective area electron diffraction (SAED). Microhardness and magnetisation testing data are also presented. A single 700 °C thermal transient was found sufficient to coarsen and partially recrystallise Eurofer 97′s tempered martensite sub-grains at the tungsten-Eurofer 97 interface. Further transient exposure at 700 °C resulted in the significant growth of equiaxed grains, the nucleation of intergranular Cr-rich M7C3 and M23C6 carbides, and the coarsening of V-rich and intra-granular Ta-rich MX precipitates. The microstructural effects of 850 °C transients are also reported. Notably, after 1,000 transients at 850 °C the hardness of Eurofer 97 was found to have decreased by 32 %.

Experimental investigation on the macro- and micromechanical properties of water-cooled granite at different high temperatures

To investigate the damage mechanisms in granite’s physical and mechanical properties after high-temperature water quenching, this study employed MTS815.04 for uniaxial compression tests on thermally treated specimens, with concurrent acoustic emission monitoring, and utilized nanoindentation for micromechanical analysis. The results show that with increasing temperature, granite's peak strength and elastic modulus decrease, with a sharp decline after 400–500 °C, corresponding to a significant increase in the internal damage, which can be detected by acoustic emission monitoring. Below 500 °C, macroscopic mechanical degradation is due to mineral thermophysical property differences, while above 500 °C, microcrack development is the main deterioration factor. The failure mode shifts from tensile to tensile-shear complex to shear failure, with transition points at 400 °C and 800 °C. The results of this study are of certain reference value for improving the efficiency of extracting thermal energy from dry-hot rocks and providing security guidance for the tunnel restoration process following fire damage.

Mechanical behavior and microstructural deformation mechanisms of Ti-6Al-4V helix springs under prolonged extreme cryogenic temperatures and constant loading

The prolonged mechanical performance degradation and failure of elastic components in mechanical systems can pose significant safety risks and disrupt related operations. While helical compression springs' mechanical behavior and failure mechanisms at high temperatures have been well-studied, their mechanical properties and microstructural deformation mechanisms at extreme cryogenic temperatures remain largely unexplored. This paper conducts experiments to investigate the detailed mechanical properties and microstructural evolution of Ti-6Al-4V helix springs under such conditions. Initially, we examined the mechanical properties at cryogenic temperatures and compared them with those at high temperatures. It was observed that the logarithmic constitutive model applicable at high temperatures does not suitably describe the spring's mechanical behavior at cryogenic temperatures. At extremely low temperatures, the mechanical properties of the spring were enhanced. Furthermore, we characterized the microstructural deformation mechanisms using electron backscatter diffraction (EBSD) and transmission electron microscopy (TEM), including twinning, slip activation, and dislocation evolution. The findings suggest that the deformation mechanism in Ti-6Al-4V springs under cryogenic conditions is predominantly governed by twinning and basal and prismatic slip. Due to the significant increase in the critical resolved shear stress (CRSS) of the pyramidal slip systems at cryogenic temperatures, these slip systems may not be activated during the deformation process. Additionally, the volume fraction of twinning shows a significant positive correlation with both cryogenic temperature and mechanical stress.

Advancements in Optoelectronics: Harnessing the Potential of 2D Violet Phosphorus

AbstractRecently, 2D violet phosphorus (VP), a new kind of allotrope of phosphorus has attained significant attention owing to its remarkable electronic, optical, and magnetic characteristics. Tunable, large direct bandgap, high charge carrier mobility, and large optical absorption make it a potential candidate for realizing photoelectronic applications. VP demonstrates unique electronic structure, chemical stability, strong light‐matter interaction, and thermal stability that can be utilized for assembling intelligent photoelectronic devices. This review article provides comprehensive investigations of the latest synthesis techniques employed to develop the VP including its structural characterizations, stability, and degradation mechanisms. Furthermore, this review demonstrates the diverse applications of VP in optoelectronics, including photodetectors, polarization detection, imaging systems, neuromorphic optoelectronic devices, and many others. Finally, challenges and future research directions associated with the VP in terms of optoelectronics are discussed. Overall, as presented, the review offers an extensive study of VP, covering its synthesis, structural insights mechanisms, and applications in optoelectronics with the aim of stimulating further research and development in this growing field.

Degradation of ciprofloxacin hydrochloride in a multiphase mixed system by subaquatic gas-liquid discharge plasma

Abstract In recent years, antibiotic pollution has become a serious threat to human health. In this paper, a gas-liquid discharge plasma is developed to degrade ciprofloxacin hydrochloride in a multiphase mixed system containing inorganic and organic impurities. The discharge characteristics are analyzed by diagnosing the applied voltage and discharge current waveforms, as well as the optical emission spectra. The work investigates how degradation efficiency is affected by applied voltage, gas flow rate, treatment time, initial concentration as well as the addition of γ-Al2O3 pellets and peanut straw. After 70 min, the degradation efficiency of ciprofloxacin hydrochloride in the multiphase mixed system reached 99.6%. Its removal efficiency increases as the initial concentration decreases and the applied voltage increases. Besides, there is still a good degradation efficiency of ciprofloxacin hydrochloride with the addition of peanut straw. The degradation mechanism of ciprofloxacin hydrochloride is investigated through the analysis of degraded intermediates and reactive species.

Efficient Photocatalytic Degradation of Triclosan and Methylene Blue by Synthesized Ag-Loaded ZnO under UV Light

Industrial discharge of hazardous organic and synthetic chemicals, such as antibacterials and dyes, poses severe risks to human health and the environment. This study was conducted to address the urgent need for efficient and stable zinc-oxide-based photocatalysts to degrade such pollutants. A novel approach to synthesizing silver-loaded zinc oxide (Ag@Z) catalysts was introduced by using a simple and efficient combination of hydrothermal and precipitation methods. Comprehensive characterization of Ag@Z photocatalysts was performed using XRD, XPS, Raman, UV–vis adsorption, FTIR, and SEM, revealing an enhancement of structural, optical, and morphological properties in comparison to pure zinc oxide. Notably, the 5%Ag@Z catalyst exhibited the highest degradation efficiency among the other synthesized catalysts under UV-C light irradiation, and enhanced the degradation rate of pure zinc oxide (Z) by 1.14 and 1.64 times, for Triclosan (TCS) and Methylene Blue (MB), respectively. the effect of catalyst dose and initial concentration was studied. A mechanism of degradation was proposed after investigating the effect of major reactive species. The 5%Ag@Z catalyst increased the photostability, which is a major problem of zinc oxide due to photocorrosion after reusability. We found that 50% and 74% of energy consumption for the photocatalytic degradation of TCS and MB by 5%Ag@Z, respectively, was saved in compassion with zinc oxide. The remarkable photocatalytic performance and the good recovery rate of Ag@Z photocatalysts demonstrate their high potential for photocatalytic degradation of organic contaminants in water.

The failure mechanism of field polyethylene gas pipeline with gas leakage at electrofusion joint

Purpose A section of in-service PE gas pipeline in Guocun, Beijing, was found to appear gas leaking at the electrofusion (EF) joint. This study is dedicated to reveal the material cause of EF joint failure to help with a more accurate prediction of service life of PE gas pipe and further normalize the construction of PE gas pipeline. Design/methodology/approach Defect detection was carried out on the leaking EF joint using ultrasonic phased array. The mechanical degradation and structural aging behavior was studied by tension test, FTIR technology, TG test and DSC test. The organic components in the soil surrounding the PE gas pipe failure area were qualitatively identified. Findings The results showed that the organic surfactants in the soil environment could accelerate the aging behavior of PE material, leading to a deterioration of mechanical properties and a serious reduction in the ability of the PE pipe and EF joint, especially at the welding defect, to resist external force. Originality/value A novel study was conducted to investigate the failure cause of the EF joint of in-service PE gas pipe, incorporating the analysis of environmental factors and structural deterioration.

In-situ compression tests and analysis of strength-ductility synergy in heterogeneous structured copper-tin composite joint

Copper-tin (Cu-Sn) serves as a prevalent alloy system in electronic packaging, envisioned for future high-power device applications. However, interdiffusion in Cu-Sn yields rigid and brittle Cu6Sn5 and Cu3Sn phases, causing joint hardening and embrittlement. This paper introduces a novel, non-homogeneous Cu-Sn composite employing heterostructure design. Through room temperature in-situ compression tests and molecular dynamics (MD) simulations, we investigate mechanical property degradation origins and Cu-Sn composite strength-ductility mechanisms. Our findings reveal hierarchical heterostructures in joints stimulate dynamic stress distribution at interfaces, generating a high density of geometrically necessary dislocations (GNDs). This enhances the material's work-hardening rate and imparts robust strain-hardening capabilities. This unique structural feature has altered the interaction between dislocations and interfaces, thereby effectively promoting the formation and driving force of dislocations. The combined effects of strain inhomogeneity induced by soft and hard phases, along with a hybrid mechanism involving stacking faults (SFs), Lomer-Cottrell (L-C) locking, and dislocation bypassing and shearing, realize exceptional strength-ductility synergies in Cu-Sn composite joints. This study presents a promising paradigm for designing microstructures in high-strength, deformable, and high-temperature-resistant soldered composites.

A ternary composite nanofibrous photocatalyst: FcLR-gC3N4/polyisothianaphthene/polyacrylonitrile for degradation of organic dyes

BackgroundWater pollution by organic dyes is one of the important environmental issues. When substances such as organic dyes are discharged into water, they can severely pollute the water and harm the life of living organisms. MethodsA new ternary composite nanofibrous photocatalyst, FcLR-gC3N4/PITN/PAN, was produced through 1) synthesis of a graphitic carbon nitride (g-C3N4)-based ferrocenyl dithiophosphonic acid, FcLR-gC3N4, by the attachment of Ferrocenyl Lawesson's Reagent (FcLR) to g-C3N4 nanosheets, 2) incorporation of the FcLR-gC3N4 into the polymeric matrix of as-prepared polyisothianaphthene (PITN) blending with polyacrylonitrile (PAN), and 3) fabrication of electrospun nanofibers (NFs) through electrospinning. Significant findingsThe degradation of methyl orange (MO) and methylene blue (MB) was more efficient on FcLR-gC3N4 compared to g-C3N4 alone, and on FcLR-gC3N4/PITN/PAN compared to FcLR-gC3N4, confirming the effective role of both FcLR and PITN/PAN matrix in the degradation of the dyes. The ternary composite nanofiber degraded 92% of MB and 29% of MO. The MB mineralization percentages of 65% (TOC), 60% (COD), and 55% (BOD) were achieved after 2 h and 30 min. Radical trapping experiments consistent with the Tauc plots and Mott-Schottky plots distinguished O2•- as the primary species in the degradation mechanism of MB. The MB degradation pathway was determined through LC-MS-MS. The electrochemical impedance spectrum (EIS) and photocurrent measurements confirmed the higher photocatalytic activity of FcLR-gC3N4 compared to g-C3N4 alone by studying the charge carrier's separation and recombination. A high recyclability was found for FcLR-gC3N4. The recycling stability of FcLR-gC3N4 increased after its embedding into the nanofibrous matrix of PITN/PAN.

Oxygen concentration regulated the efficient liquefaction of vulcanized natural rubber

Oxidative liquefaction represents a promising avenue for the homogeneous and high-value utilization of waste tire rubber. Given that truck tires predominantly comprise natural rubber (NR), this study investigated the efficient liquefaction of vulcanized NR regulated by oxygen concentration. Remarkably, the liquefaction of vulcanized NR was realized with an oxygen concentration of 75% at 200°C within 3 min. FTIR spectroscopy showed that carbonyl, ether and sulphoxide groups were produced during the liquification of NR vulcanizates. Oxygen concentration significantly affected the oxidative efficiency of both the main chains and crosslinks, with a more pronounced effect observed on the main chains. Nevertheless, the similar molecular weights and polydispersity indices across various degraded products suggested a selective oxidative cleavage of the NR backbone. Furthermore, online ATR-FTIR was used to monitor the dynamic changes of NR's molecular structure to elucidate the oxidative degradation mechanism. The oxidative cleavage of NR main chain primarily occurred at the C-C bonds connected with allyl groups, producing oxidized products enriched with conjugated carbonyl groups. Alternatively, the main chain scission may also occur due to the electronic rearrangement effect of the C=C bond and produce saturated carbonyl groups. Oxygen concentration modulated the degradation efficiency of vulcanized NR, which provided an efficient strategy for the upcycling of NR-based waste tires.

Magnetic Nitrogen-Doped Fe<sub>3</sub>C@ c Catalysts for Efficient Activation of Peroxymonosulfate for Degradation of Organic Pollutants

Recoverable and stable nanocatalysts are essential for peroxymonosulfate - based advanced oxidation processes (AOPs) in wastewater purification treatment. In this paper, Fe3C nanorods @ nitrogen-doped carbon composites (N-Fe3C@C) with core-shell architecture were fabricated by the co-precipitation and calcination methods, and characterized and analyzed in terms of their crystal structure, microscopic morphology, and surface chemical elements. In addition, N-Fe3C@C-4 degraded 85.36% of tetracycline in 10 min under PMS, which was much higher than the catalytic ability of Fe3O4 (42.03% in 10 min). Both the active radical trapping and EPR experiments verified that 1O2 played a key role for degradation of organic dyes in PMS system. The investigation on the degradation mechanism revealed that the presence of the carbon layer facilitated to adsorb TC, accelerate free radical generation and promote the redox cycle of Fe2+/Fe3+ in the nanocatalyst. This study offers novel ideas for multifunctional catalysts for advanced wastewater purification treatment.

Connexin43 promotes exocytosis of damaged lysosomes through actin remodelling.

A robust and efficient cellular response to lysosomal membrane damage prevents leakage from the lysosome lumen into the cytoplasm. This response is understood to happen through either lysosomal membrane repair or lysophagy. Here we report exocytosis as a third response mechanism to lysosomal damage, which is further potentiated when membrane repair or lysosomal degradation mechanisms are impaired. We show that Connexin43 (Cx43), a protein canonically associated with gap junctions, is recruited from the plasma membrane to damaged lysosomes, promoting their secretion and accelerating cell recovery. The effects of Cx43 on lysosome exocytosis are mediated by a reorganization of the actin cytoskeleton that increases plasma membrane fluidity and decreases cell stiffness. Furthermore, we demonstrate that Cx43 interacts with the actin nucleator Arp2, the activity of which was shown to be necessary for Cx43-mediated actin rearrangement and lysosomal exocytosis following damage. These results define a novel mechanism of lysosomal quality control whereby Cx43-mediated actin remodelling potentiates the secretion of damaged lysosomes.

Profiling Cellular Morphological Changes Induced by Dual-Targeting PROTACs of Aurora Kinase and RNA-Binding Protein YTHDF2.

Proteolysis targeting chimeras (PROTACs) are new chemical modalities that degrade proteins of interest, including established kinase targets and emerging RNA-binding proteins (RBPs). Whereas diverse sets of biochemical, biophysical and cellular assays are available for the evaluation and optimizations of PROTACs in understanding the involved ubiquitin-proteasome-mediated degradation mechanism and the structure-degradation relationship, a phenotypic method profiling the cellular morphological changes is rarely used. In this study, first, we reported the only examples of PROTACs degrading the mRNA-binding protein YTHDF2 via screening of multikinase PROTACs. Second, we reported the profiling of cellular morphological changes of the dual kinase- and RBP-targeting PROTACs using the unbiased cell painting assay (CPA). The CPA analysis revealed the high biosimilarity with the established aurora kinase cluster and annotated aurora kinase inhibitors, which reflected the association between YTHDF2 and the aurora kinase signaling network. Broadly, the results demonstrated that the cell painting assay can be a straightforward and powerful approach to evaluate PROTACs. Complementary to the existing biochemical, biophysical and cellular assays, CPA provided a new perspective in characterizing PROTACs at the cellular morphology.