Local Concentration Research Articles

Achieving superior strength-ductility balance by tailoring dislocation density and shearable GP zone of extruded Al-Cu-Li alloy

Pre-stretching is commonly employed to accelerate ageing precipitation kinetics in wrought Al-Cu-Li alloys, but uneven precipitation resulting from dislocation pile-ups often degrades ductility. Herein, the strength and ductility of extruded Al-Cu-Li alloy are significantly improved through a novel thermomechanical treatment, involving pre-ageing and pre-stretching, followed by low-temperature interrupted ageing. A superior balance between high yield strength (∼ 657 MPa) and good ductility (elongation to fracture of ∼ 13.5 %) is obtained, with elongation increased by 105 % compared to the conventional T8 temper, while maintaining a respectable yield strength. Microstructure analysis reveals that dense Guinier–Preston (GP) zones induced by pre-ageing effectively dissipate energy from dislocation sliding, resulting in a uniform dislocation configuration even at 8 % pre-stretching. However, the GP zone density is greatly reduced due to their dissolution following pre-stretching. Upon interrupted ageing, the reprecipitation of GP zones forms a homogeneous mixture of δ′, GP zones, and T1 phases. This combination alleviates local stress concentrations and lengthens the dislocation mean free path during tensile testing by shearing the GP zones at multiple sites, thereby improving ductility. Simultaneously, T1 precipitates strengthen the alloy by pinning dislocations and promoting dislocation cross-slip, improving work hardening capacity. The dissolution of GP zones also redistributes the Cu atoms within the matrix, further enhancing the intrinsic ductility of the Al matrix. These findings offer valuable insights for developing high-performance wrought Al-Cu-Li alloys.

Surface-controlled oxygen vacancy-rich Bi/BiVO4 Schottky junction for highly selective and active photocatalytic nitrogen fixation

The modulation of active site density and localized electron concentration represents a crucial step in enhancing nitrogen activation, thereby significantly augmenting the efficiency of photocatalytic nitrogen fixation. In this paper, Bi/BiVO4 Schottky junctions enriched with oxygen vacancies (Bi/Vo-BVO) were fabricated by in situ reduction. Compared to BiVO4, Bi/Vo-BVO composites exhibited 8.4-fold enhancement in ammonia synthesis yield, reaching a maximum rate of 167.74 μmol·g−1·h−1. In situ FTIR spectroscopy and isotopic labeling experiments definitively demonstrated that the nitrogen constituent of NH4+ is derived from N2. N2-TPD and DFT calculation collectively suggest that the surface of Bi/Vo-BVO, enriched with ligand-unsaturated V4+ species, furnishes a substantial array of chemisorption sites for N2 molecules, attributed to the abundance of oxygen vacancies. In situ XPS coupled with DFT corroborate that the photoexcited electrons within the BiVO4 valence band accumulate in the conduction band, thereby directly facilitating the activation of N2 adsorbed at the V4+ active sites; The built-in electric field established at the interface between Bi and BiVO4 substantially facilitates the enrichment of Bi-emitted thermal electrons within oxygen vacancies on BiVO4 surface. These electrons subsequently migrate towards and interact with the adsorbed N2 via the V4+ active sites. The synergistic photothermal electrons activation mechanism of N2 not only enhances the efficiency of light energy utilization but maximizes the catalytic efficacy of the photocatalyst through the full exploitation of its intrinsic catalytic potential.

Implicit Solvent with Explicit Ions Generalized Born Model in Molecular Dynamics: Application to DNA.

The ion atmosphere surrounding highly charged biomolecules, such as nucleic acids, is crucial for their dynamics, structure, and interactions. Here, we develop an approach for the explicit treatment of ions within an implicit solvent framework suitable for atomistic simulations of biomolecules. The proposed implicit solvent/explicit ions model, GBION, is based on a modified generalized Born (GB) model; it includes separate, modified GB terms for solute-ion and ion-ion interactions. The model is implemented in the AMBER package (version 24), and its performance is thoroughly investigated in atomistic molecular dynamics (MD) simulations of double-stranded DNA on a microsecond time scale. The aggregate characteristics of monovalent (Na+ and K+) and trivalent (Cobalt Hexammine, CoHex3+) counterion distributions around double-stranded DNA predicted by the model are in reasonable agreement with the experiment (where available), all-atom explicit water MD simulations, and the expectation from the Manning condensation theory. The radial distributions of monovalent cations around DNA are reasonably close to the ones obtained using the explicit water model: expressed in units of energy, the maximum deviations of local ion concentrations from the explicit solvent reference are within 1 kBT, comparable to the corresponding deviations expected between different established explicit water models. The proposed GBION model is able to simulate DNA fragments in a large volume of solvent with explicit ions with little additional computational overhead compared with the fully implicit GB treatment of ions. Ions simulated using the developed model explore conformational space at least 2 orders of magnitude faster than in the explicit solvent. These advantages allowed us to observe and explore an unexpected "stacking" mode of DNA condensation in the presence of trivalent counterions (CoHex3+) that was revealed by recent experiments.

Extraction of rare earth ions using thermomorphic ionic liquid: In situ spatial and temporal distribution combined with thermodynamic description

Homogeneous Liquid–Liquid Extraction (HLLE) provides a valuable opportunity for recycling Rare Earth Elements (REE) by circumventing the liquid–liquid interface and avoiding the problems linked to the high viscosity of ionic liquids (IL). For optimizing these processes with the ultimate goal of implementing them at the industrial scale, it is crucial to understand the mechanisms at play at various scales. In this study, we focused on the extraction of two REE elements, La(III) and Ce(III) with an HLLE system composed of the IL [Chol][TFSI], water and betaine as the extractant. We first established the phase diagram of [Chol][TFSI]/betaine/water using 1H nuclear magnetic resonance (NMR) spectroscopy. We then determined the efficiency E and distribution ratio D of the HLLE for different betaine concentrations. HLLE was modeled thermodynamically to access the most likely number of betaine molecules involved in the extraction process, which appears to be 2. Finally, we monitored in situ the extraction using X-ray Absorption Spectroscopy (XAS) at the K-edge of both lanthanum and cerium. It allowed us on one hand, to get some insight into the local environment around the REE, and on the other hand to measure the local concentration of REE at each position within the extraction system. In this latter process, we could evidence an accumulation of REE accumulates close to the liquid–liquid interface, a feature that was suggested by some recent simulations.

Progressive damage and stiffness degradation assessments of double‐lap CFRP/Ti interference fit bolted joints under quasi‐static tensile load

AbstractMatrix crack propagation and stiffness degradation behaviors of the carbon fiber reinforced polymer/titanium alloy (CFRP/Ti) bolted joint were characterized by a synergistic damage mechanics approach. The parametric study including pre‐tightening torques and interference fit sizes was conducted. The results showed that the joint stiffness degradation exhibited characteristics of local stiffness degradation due to local stress concentration. Stiffness degradation in different plies was caused by matrix crack damage occurring in different directions. The pre‐tightening torque significantly increased the joint stiffness and restrain matrix crack progression, effectively inhibiting the stiffness degradation of the joint. Moreover, the low interference fit level delayed the crack initiation in −45° ply and 45° ply and the crack propagation of the laminate, while promoted the crack initiation in 90° ply. The stiffness degradation of the laminate could be significantly reduced by interference fit.Highlights Matrix crack propagation and stiffness degradation behaviors of the CFRP laminate were characterized by a synergistic damage mechanics method. A FE model of the CFRP/Ti double‐lap interference fit bolted joint was established. Influences of pre‐tightening torques on both matrix crack initiation and propagation were investigated. The optimum interference fit size of the matrix damage strengthening was 0.20%–0.60%.

389 Impact of a Controlled Internal Drug Release device on circulating and local concentrations of progesterone

Abstract Controlled Internal Drug Release (CIDR) devices have become an important component of reproductive management programs in many beef herds. When a CIDR is inserted into a cow, circulating concentrations of progesterone mimic a functional corpus luteum. Some data, however, suggest that concentration of progesterone following insertion of a CIDR might have negative consequences on fertility in Bos indicus animals. Therefore, the objective of this study was to determine the impact of a CIDR device on circulating and uterine tissue concentrations of progesterone. A blood sample and a uterine biopsy were collected from non-suckled postpartum cycling Brahman cows (n = 10; Cycling) during the midluteal stage. A blood sample and a uterine biopsy were also collected from non-suckled postpartum cycling Brahman cows (n = 9; CIDR) after a CIDR had been in place for 5 d. To collect uterine biopsies from CIDR cows, the uterine biopsy tool was placed inside a plastic covering, both were passed into the cervix of the cow before the tool was extended through the covering and into the uterus. After the biopsy was collected, the tool was carefully removed to prevent sample contamination. Blood samples were centrifuged, and serum was collected to determine concentrations of progesterone. Uterine biopsies were snap frozen until extraction. Biopsies were weighted, thawed, and homogenized in assay buffer. Samples were then extracted with methyl tert-butyl ether and resuspended in assay buffer. Serum concentrations are reported as ng/mL and uterine concentrations are reported as ng/g. Statistical analysis was performed using the GLM procedure in SAS with treatment (CIDR vs Cycling), tissue type (uterine vs serum) and their interaction included in the model. There was a significant effect of treatment (P = 0.0062), tissue (P = 0.0063) and a treatment by tissue interaction (P = 0.0068). Animals with a CIDR had greater concentrations of progesterone than Cycling animals (274.77 vs 4.37 ng, respectively). Uterine samples had greater concentrations of progesterone than serum samples (274.40 vs 4.74 ng, respectively). These increased concentrations of progesterone were mainly from CIDR uterine samples (543.24 ng/g) which had greater (P < 0.001) concentrations of progesterone compared with all other samples, which did not differ from each other (P > 0.98; CIDR Serum 6.29 ng/mL, Cycling Serum 3.2 ng/mL, and Cycling Uterus 5.54 ng/g). In summary, CIDRs increased circulating concentrations of progesterone sufficient to keep animals from exhibiting estrus, and were not different from cows in the midluteal stage of their cycle. Local concentrations in uterine tissue; however, were significantly greater when a CIDR was in place compared with uterine tissue collected during the midluteal phase. The implications of these significantly greater concentrations of progesterone in uterine tissue warrant further investigation.

Polymeric Antibiotic Beads for Canine Osteomyelitis: Advancing Localized Antibiotic Treatment with Enhanced Efficacy and Minimized Side Effects

Antibiotic beads represent a compelling treatment method for the treatment and prevention of canine osteomyelitis, as they provide localized antibiotic concentrations at the infection site with minimal systemic toxicity. The therapeutic efficacy of these beads has been demonstrated, highlighting their potential as a valuable local antibiotic therapy. In particular, the introduction of vancomycin - polymethylmethacrylate (PMMA) beads is highlighted as a promising new form of local antibiotic therapy. This article focuses on the use of antibiotic-impregnated beads to treat localized bacterial infections in the bones and joints of canines. Typically composed of poly(lactic-co-glycolic acid) (PLGA) or polymethylmethacrylate (PMMA), these beads contain antibiotics such as vancomycin, placed directly into the affected area, providing a high antibiotic concentration at the site of infection. These beads were developed for a slow antibiotic release over time; they ensure a constant protective effect against a broad spectrum of bacteria, demonstrating high efficacy and biocompatibility with the animal's body. This localized antibiotic treatment option offers several advantages over systemic antibiotics, such as reduced side effects and improved efficacy. It could be a promising option for the treatment of bone and joint infections in canines.

Efficacy of a novel oxygen scavenger mask in reducing local oxygen concentrations below the surgical fire risk threshold: an experimental proof-of-concept study

BackgroundThis study aims to evaluate the efficacy of an oxygen scavenging mask device in reducing local oxygen concentrations from nasal cannula ventilation compared to a standard open facial surgical field.MethodsThis is a controlled experiment using a custom-fabricated silicone midfacial oxygen scavenging device, SimMan airway management trainer manikin (Laerdal Medical, Stavanger, Norway), handheld oxygen detector (Forensics Detectors, Los Angeles, United States) and oxygen from a Datex Ohmeda Aisys Carestation anesthesia unit (GE HealthCare, Chicago, United States). Oxygen concentrations were measured at 18 facial landmarks (Fig. 1) with nasal cannula flow of 2, 4, and 6 L/min of 100% FiO2 in both masked and unmasked conditions (Fig. 2).ResultsThe mean oxygen concentration in the facial surgical field was 20.95% with the scavenger mask and 24.8% without (P < 0.001; two-tailed paired t-test). The unmasked condition was associated with suprathreshold oxygen concentration levels at 13 of 18 facial landmarks (Table 1). The device significantly reduced local oxygen concentration at 16 of 18 facial landmarks (Table 1). The device provided safe oxygen concentration levels at all three flow rates, and measured oxygen concentrations directly correlated with oxygen flow rate in the unmasked condition (Table 2).ConclusionsAn oxygen scavenger mask device reduced local oxygen concentrations from nasal cannula ventilation to below the 23% fire threshold in the entire facial surgical field external to the mask in these experiments. The device may reduce intraoperative fire risk in patients that require supplementary oxygen during surgery.

Multifunctional fluorinated phosphonate-based localized high concentration electrolytes for safer and high-performance lithium-based batteries

This study introduces a novel fluorinated phosphonate-based additive, Bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate (BTCMP), in a localized high-concentration electrolyte (LHCE) to address key challenges in lithium metal batteries (LMBs), such as dendritic lithium growth and porous electrode morphology. The pristine LHCE forms a fluorine-rich solid electrolyte interphase (SEI) layer, primarily composed of lithium fluoride (LiF). However, the pristine LHCE suffers from severe electrolyte decomposition, forming a thicker and more resistive cathode electrolyte interphase (CEI), leading to increased impedance and reduced cyclability. Interestingly, Density Functional Theory (DFT) investigations revealed that the BTCMP inclusion modifies the solvation structure by dispersing the aggregates into smaller fragments, facilitating easier Li+ migration than the pristine LHCE. The addition of BTCMP suppresses solvent decomposition as confirmed by an increasing trend in the lowest unoccupied molecular orbital (LUMO) of corresponding LHCE molecules. Further, the presence of BTCMP results in a thinner and more stable CEI, reducing electrolyte decomposition, maintaining better ion transport, and preserving the cathode's structural integrity, as supported by TEM and XPS analysis. The BTCMP-based F-rich LHCE retained 82 % of its initial capacity while maintaining a coulombic efficiency of 99.5 % after 200 cycles in a Li||LNMO cell while the pristine LHCE only retained 47.2 % of initial capacity post-150 cycles. Additionally, the flame-retardant properties of BTCMP-based LHCE highlight its safety compared to commercial electrolytes.

Engineering Adhesion of the Probiotic Strain Escherichia coli Nissle to the Fungal Pathogen Candida albicans.

Engineering live biotherapeutic products against fungal pathogens such as Candida albicans has been suggested as a means to tackle the increasing threat of fungal infections and the development of resistance to classical antifungal treatments. One important challenge in the design of live therapeutics is to control their localization inside the human body. The specific binding capability to target organisms or tissues would greatly increase their effectiveness by increasing the local concentration of effector molecules at the site of infection. In this study, we utilized surface display of carbohydrate binding domains to enable the probiotic E. coli Nissle 1917 to adhere specifically to the pathogenic yeast Candida albicans. Binding was quantified using a newly developed method based on the automated analysis of microscopic images. In addition to a rationally selected chitin binding domain, a synthetic peptide of identical length but distinct sequence also conferred binding. Efficient binding was specific to fungal hyphae, the invasive form of C. albicans, while the yeast form, as well as abiotic cellulose and PET particles, was only weakly recognized.

Manipulation of Oxygen Species on an Antimony-Modified Copper Surface to Tune the Product Selectivity in CO2 Electroreduction.

Rational regulation of the electrochemical CO2 reduction reaction (CO2RR) pathway to produce desired products is particularly interesting, yet designing economical and robust catalysts is crucial. Here, we report an antimony-modified copper (CuSb) catalyst capable of selectively producing both CO and multicarbon (C2+) products in the CO2RR. At a current density of 0.3 A/cm2, the faradaic efficiency (FE) of CO was as high as 98.2% with a potential of -0.6 V vs reversible hydrogen electrode (RHE). When the current density increased to 1.1 A/cm2 at -1.1 V vs RHE, the primary products shifted to C2+ compounds with a FE of 75.6%. Experimental and theoretical studies indicate that tuning the potential could manipulate the oxygen species on the CuSb surface, which determined the product selectivity in the CO2RR. At a more positive potential, the existence of oxygen species facilitates the potential-limiting step involving *COOH formation and reduces the adsorption of *CO intermediates, thereby promoting CO production. At a more negative potential, the localized high CO concentration coupled with the enhanced adsorption of *CO intermediates due to Sb incorporation facilitates C-C coupling and deep hydrogenation processes, resulting in an increased C2+ selectivity.

New insights from crystallography into the effect of Ni content on ductile-brittle transition temperature of 1000 MPa grade high-strength low-alloy steel

The significant effect of Ni content (0.92, 1.94 and 2.94 wt%) on ductile-brittle transition temperature (DBTT) and microstructure in a 1000 MPa grade high-strength low-alloy (HSLA) steel was studied. Using scanning electron microscopy (SEM), electron backscatter diffraction (EBSD), transmission electron microscopy (TEM), Charpy impact test and low-temperature tensile test to study the fundamental reasons for the effect of Ni content on toughness. The results indicated that increasing the Ni content can reduce the DBTT of HSLA steel and improve the impact toughness at low temperatures. EBSD data post-processing analysis revealed that the key reason for the increase in low-temperature toughness is the refinement of the microstructural crystallographic structure, specifically the significant increase in the boundary density of the block and packet. With the increase of Ni content, the density of grain boundary with an orientation difference greater than 5° between two adjacent {110} crystal planes was higher, which can form a higher density of dislocation pile-up group, thus better reducing local stress concentration. Meanwhile, the stacking fault energy (SFE) increases with the increase of Ni content, which made the screw dislocation more prone to cross slip at low temperature, resulting in an increase in plasticity at low temperatures. These observed phenomena and reasons provided a theoretical explanation for the role of Ni content in reducing DBTT and enhancing the toughness of the core in heavy gauge plates.

Mechanism of BRCA1-BARD1 function in DNA end resection and DNA protection.

DNA double-strand break (DSB) repair by homologous recombination is initiated by DNA end resection, a process involving the controlled degradation of the 5'-terminated strands at DSB sites1,2. The breast cancer suppressor BRCA1-BARD1 not only promotes resection and homologous recombination, but it also protects DNA upon replication stress1,3-9. BRCA1-BARD1 counteracts the anti-resection and pro-non-homologous end-joining factor 53BP1, but whether it functions in resection directly has been unclear10-16. Using purified recombinant proteins, we show here that BRCA1-BARD1 directly promotes long-range DNA end resection pathways catalysed by the EXO1 or DNA2 nucleases. In the DNA2-dependent pathway, BRCA1-BARD1 stimulates DNA unwinding by the Werner or Bloom helicase. Together with MRE11-RAD50-NBS1 and phosphorylated CtIP, BRCA1-BARD1 forms the BRCA1-C complex17,18, which stimulates resection synergistically to an even greater extent. A mutation in phosphorylated CtIP (S327A), which disrupts its binding to the BRCT repeats of BRCA1 and hence the integrity of the BRCA1-C complex19-21, inhibits resection, showing that BRCA1-C is a functionally integrated ensemble. Whereas BRCA1-BARD1 stimulates resection in DSB repair, it paradoxically also protects replication forks from unscheduled degradation upon stress, which involves a homologous recombination-independent function of the recombinase RAD51 (refs. 4-6,8). We show that in the presence of RAD51, BRCA1-BARD1 instead inhibits DNA degradation. On the basis of our data, the presence and local concentration of RAD51 might determine the balance between the pronuclease and the DNA protection functions of BRCA1-BARD1 in various physiological contexts.

Market power and wages: evidence from Brazil

PurposeThe paper examines the impact of market power on wages within the context of a developing country, focusing on Brazil.Design/methodology/approachWith access to matched employer–employee data from Brazil, we first characterized the evolution of the local labor market concentration (Municipality Herfindahl–Hirschman Index [HHI]). Then, we built a fixed-effect model with instrumental variables to verify the association between the local labor market concentration and wages. Finally, a difference-in-difference (DiD) was implemented to verify whether a merger transaction impacted the workers’ earnings in the Brazilian banking sector.FindingsThe paper’s findings suggest that there may be a negative relationship between market power and workers’ earnings.Originality/valueThis research conducted an in-depth investigation of the labor market power in a developing country. As far as we know, our work is the first to evaluate the extension of local concentration in Brazilian formal labor markets and to illustrate its evolution over the last decades. Additionally, when going through the effects of market concentration on wages, we use a new identification strategy that explores changes in the HHI that are caused by national trends in an industry as a source of exogenous variation. Finally, the last part of the paper assesses the effects of antitrust policy on the labor market, a kind of investigation that is still scarce.

A venom peptide-induced NaV channel modulation mechanism involving the interplay between fixed channel charges and ionic gradients

Venoms are used by arthropods either to immobilise prey or as defence against predators. Our study focuses on the venom peptide, Ta3a, from the African ant species, Tetramorium africanum and its effects on voltage-gated sodium (NaV) channels, which are ion channels responsible for the generation of electrical signals in electrically excitable cells, such as neurons. Using the NaV1.7 isoform as our model NaV channel we show that Ta3a prolongs single channel active periods with increased open probability and induces non-inactivating whole-cell currents. Ta3a-affected NaV1.7 channels exhibit a leftward (hyperpolarising) shift in activation threshold, constitutive activity even in the absence of an activating voltage stimulus, and at cell membrane voltages where channels are normally silent. Current-voltage experiments show that Ta3a shifts the voltage at which NaV current changes direction (reversal potential) by altering the local ionic concentration of permeant ions (Na+) rather than changing the channel’s preference for ionic species. We propose a model where Ta3a maintains the positively charged voltage-sensing (S4) domains of the channel in the activated configuration where their electric field is exposed to the extracellular membrane surface to create an ionic bilayer comprising S4 domains and mobile anions (Cl−). This bilayer has a depolarising effect on the cell membrane, thus reducing the amount of externally applied voltage required for channel activation.

Stable Lithium Oxygen Batteries Enabled by Solvent-diluent Interaction in N,N-dimethylacetamide-based Electrolytes.

In the pursuit of next-generation ultrahigh-energy-density Li-O2 batteries, it is imperative to develop an electrolyte with stability against the strong oxidation environments. N,N-dimethylacetamide (DMA) is a recognized solvent known for its robust resistance to the highly reactive reduced oxygen species, yet its application in Li-O2 batteries has been constrained due to its poor compatibility with the Li metal anode. In this study, a rationally selected hydrofluoroether diluent, methyl nonafluorobutyl ether (M3), has been introduced into the DMA-based electrolyte to construct a localized high concentration electrolyte. The stable -CH3 and C-F bonds within the M3 structure could not only augment the fundamental properties of the electrolyte but also fortify its resilience against attacks from O2 - and 1O2. Additionally, the strong electron-withdrawing groups (-F) presented in the M3 diluent could facilitate coordination with the electron-donating groups (-CH3) in the DMA solvent. This intermolecular interaction promotes more alignments of Li+-anions with a small amount of M3 addition, leading to the construction of an anion-derived inorganic-rich SEI that enhances the stability of the Li anode. As a result, the Li-O2 batteries with the DMA/M3 electrolyte exhibit superior cycling performance at both 30 °C (359th) and -10 °C (120th).

Investigating the simulation test and acoustic emission characteristics of structural-control type rockbursts in deep underground environments

Deep underground projects are in a complex in-situ stress environment, and rock burst disasters induced by the hard and brittle failure of the rock mass are prone to occur around the tunnel openings. In this study, we aim to investigate the impacts of geological weak surfaces in rock masses on rockbursts and the spatiotemporal evolution of microcracks during the development of rockbursts. To achieve this objective, two sets of cubic specimens containing a circular through-hole were designed. One set of specimens had prefabricated unfilled cracks around the openings. Subsequently, the rockburst development process within the deep tunnel was replicated by subjecting both groups of specimens to identical gradient loading using a true triaxial test system. During the test, a micro camera was used to record the failure of the borehole wall in real-time, and an acoustic emission monitoring system was utilized to capture the stress waves released during structural damage. Finally, a multi-level synergistic analysis of the rockburst damage mechanism was carried out based on the macro-imaging data and micro-acoustic emission data. The results show that failure in high-stress environments within tunnels mainly includes microcrack initiation, particle ejection, crack propagation, local cracking, slabbing spalling, damage penetration, and rockburst damage. The time–frequency domain information of acoustic emission signals is highly perceptive and representative of the structural damage state of the specimens. The mutation characteristics observed in time-domain parameters, such as acoustic emission amplitude, event rate, ringing, and cumulative energy, correspond to drastic alterations in the internal structure of the rock. The distribution characteristics of frequency-domain parameters, such as acoustic emission peak frequency, dominant frequency energy, and frequency centroid, reflect different crack scales and damage modes. The diffusion of frequency centroid indicates that the damage and failure patterns within the rock are evolving towards a more complex direction. The energy magnitude of acoustic emissions represents the damage intensity during the development of rockburst. The root causes of induced structural-control type rockbursts in deep hard brittle rock masses are the combined effects of localized high-stress concentrations and large-scale discontinuous geological structures, such as natural joints, fissures, and structural planes. The naturally occurring large-scale through-type geological weak surfaces within the rock mass reduce the strength of the surrounding rock, alter the location of stress concentration, and change the initial damage characteristics. Moreover, they promote the evolution of rockbursts, thereby increasing their destructive intensity.

Preclinical evaluation of a novel antibiotic-eluting BioEnvelope for CIED infection prevention

The risk of infection remains a significant concern with cardiovascular implantable electronic devices, necessitating the development of new strategies. This study explores the efficacy of a novel antibiotic-eluting biologic envelope designed to mitigate infection risk through localized antibiotic delivery while preserving the regenerative properties of biological matrix. Antibiotics, rifampin and minocycline, are released through polymer discs, ensuring extended drug release. Utilizing an established model of infection in a New Zealand White rabbit, the study assessed performance against Gram-positive bacterial strains, including common pathogens such as Staphylococcus aureus and S. epidermidis associated with CIED infections, and Gram-negative bacterial strains. Results demonstrated strong antibacterial activity, achieving complete eradication of bacterial colonies and greater than 6-log reductions in colonization for all strains. Pharmacokinetic analysis revealed sustained local antibiotic concentrations at the implantation site for up to 14 days, with minimal systemic exposure, demonstrating the advantages of localized drug delivery. Health outcomes in the antibiotic bioenvelope group were significantly improved, with no signs of infection or abnormal body temperatures, in contrast to the control group. Macroscopic examinations post-necropsy confirmed the absence of infection at the implantation sites of animals receiving the antibiotic bioenvelope. The combination of localized antibiotic delivery in a regenerative matrix positions the antibiotic bioenvelope as a promising solution for preventing CIED-related infections.

Stable Lithium Oxygen Batteries Enabled by Solvent‐diluent Interaction in N,N‐dimethylacetamide‐based Electrolytes

AbstractIn the pursuit of next‐generation ultrahigh‐energy‐density Li−O2 batteries, it is imperative to develop an electrolyte with stability against the strong oxidation environments. N,N‐dimethylacetamide (DMA) is a recognized solvent known for its robust resistance to the highly reactive reduced oxygen species, yet its application in Li−O2 batteries has been constrained due to its poor compatibility with the Li metal anode. In this study, a rationally selected hydrofluoroether diluent, methyl nonafluorobutyl ether (M3), has been introduced into the DMA‐based electrolyte to construct a localized high concentration electrolyte. The stable −CH3 and C−F bonds within the M3 structure could not only augment the fundamental properties of the electrolyte but also fortify its resilience against attacks from O2− and 1O2. Additionally, the strong electron‐withdrawing groups (−F) presented in the M3 diluent could facilitate coordination with the electron‐donating groups (−CH3) in the DMA solvent. This intermolecular interaction promotes more alignments of Li+‐anions with a small amount of M3 addition, leading to the construction of an anion‐derived inorganic‐rich SEI that enhances the stability of the Li anode. As a result, the Li−O2 batteries with the DMA/M3 electrolyte exhibit superior cycling performance at both 30 °C (359th) and −10 °C (120th).

Three-dimensional phase field modeling, orientation prediction and stress field analyses of twin-twin, twin-grain boundary reactions mediated by disclinations in hexagonal close-packed metals

Crystalline defects, such as dislocations, disclinations, twins and grain boundaries, play critical roles in determining the mechanical properties of metals and alloys. In particular, with multiple competitive deformation modes activated, the mechanical behaviors of hexagonal close-packed metals are strongly influenced by the interactions and reactions of various types of defects. Despite extensive studies on the elastic interactions of defects, a theoretical framework capturing crystallographic reactions, especially reaction products and associated local stress concentration, is still unavailable. Here we suggest a disclination-based method to quantify defect reactions. By using a combination of crystallographic calculations and phase field modeling/simulations, twin-twin and twin-grain boundary reactions in hexagonal close-packed metals have been quantitatively analyzed. It has been found that partial disclinations, accompanied with other defects (e.g., {112¯6} and {112¯2} high-index twins), can be generated by defect reactions as typical byproducts. The orientation change and stress fields caused by disclination formation have been systematically calculated, which offers a rigorous mathematical foundation to explore twin-twin, twin-grain boundary reactions. By quantitatively determining defect reactions and local stress fields, our work provides new insights into the deformation mechanism and microstructure-property relationship in metallic materials.