Interaction Forces Research Articles

Thermodynamic potential and drag force of the impurity-polariton many-body interaction

Investigating the many-body interaction among polaritons is a fundamental goal in comprehending nonlinear behaviors in microcavity semiconductor systems. Hence, the present study focuses on exploring the many-body interaction between excitons and impurities. It was observed that the energy eigenequation governing this system is of sixth-order, rendering it unsolvable. Consequently, a strategy involving the utilization of impurity weight was employed to partition the initial energy eigenequation into two fourth-order equations, a method deemed suitable for lower order approximations. Subsequently, Green’s function was applied to these two fourth-order equations. The analysis of the computed results, encompassing the energy spectrum, polariton density, and thermodynamic potential of the system, reveals that the many-body interaction between excitons and impurities induces the emergence of novel bound states of quasiparticles. Moreover, the inclusion of impurities leads to a decrease in both energy and density of polaritons. Furthermore, the investigation delves into the drag force exerted by impurities on excitons, demonstrating that the drag force escalates in a second-order fashion with impurity velocity and persists even as impurity velocity increases, surpassing the Landau’s equilibrium theory.

Topological constraints-induced radiation shielding efficiency of SiO2 α-cristobalite polymorphism: Signatures from Hirshfeld pseudo-surfaces

The paper presents a synergetic and comprehensive investigation into γ-radiation shields properties on SiO2 α-cristobalite subject varying external pressures (0<p < 9.1 GPa). Utilizing crystallographic methods involving γ-rays and Hirshfeld pseudo-surface (HPSs) analyses, we explore the structural responses of SiO2 α-cristobalite to external pressure and its consequent impact on MAC and LAC. The study encompasses a broad energy range (0.015<E < 15.0 MeV), employing online tool for analysis. Our findings reveal that the fundamental shielding characteristics of SiO2 α-cristobalite, including (5.809<MAC<0.021 cm2/g), (3.10 × 1023<Neff< 3.74 × 1023 e/g), (10.32<Zeff<12.43), and (10.79<Zeq<11.56), remain reliable across different polymorphic forms within the energy domain and varying pressures. The LAC values exhibit a clear dependency on both incident photon energies where it's LAC ∈ [0.042 to 11.776] cm−1 as pressure elevated on the crystal. This relationship underscores the influence of pressure-induced changes in crystal density on LAC values. Additionally, changes in lattice parameters (4.975<a<4.599 Å) and bond lengths under pressure contribute to this observed variation in the LAC values. Further analysis of the topological constraints (TCs) (i.e., 1.603<Si⋯O < 1.610 Å, 111.42°<O⋯Si⋯O < 112.00°, and 146.49°<Si⋯O⋯Si < 127.80° bending and twisting angles respectively) reveals defined correlations with LAC values.HPS topological analyses were also employed shed light on valuable insights into the mutual forces of interaction between atoms in the crystal unit cell. Changes in external stress lead to transformations in the HPSs, reflecting the impact of pressure on topological constraints. The evolution of HPS volume (i.e., 179.59-35.24 Å3) and area (i.e., 205.73-161.51 Å2) as well as void's volume (i.e., 10.20-0.17 Å3) and surface area (i.e., 46.10-3.12 Å2) within the crystal lattice is also observed, indicating a direct relationship between HPSs, crystal compactness, electron density and radiation effectiveness. These signatures have been correlated with TCs and thus on the γ-rays shield effectiveness.

Using metabolic abnormalities of carriers in the neonatal period to evaluate the pathogenicity of variants of uncertain significance in methylmalonic acidemia.

To accurately verify the pathogenicity of variants of uncertain significance (VUS) in MUT and MMACHC genes through mass spectrometry and silico analysis. This multicenter retrospective study included 35 participating units (ClinicalTrials.gov ID: NCT06183138). A total of 3,071 newborns (within 7 days of birth) were sorted into carrying pathogenic/likely pathogenic (P/LP) variants and carrying VUS, non-variant groups. Differences in metabolites among the groups were calculated using statistical analyses. Changes in conservatism, free energy, and interaction force of MMUT and MMACHC variants were analyzed using silico analysis. The percentage of those carrying VUS cases was 68.15% (659/967). In the MMUT gene variant, we found that C3, C3/C2, and C3/C0 levels in those carrying the P/LP variant group were higher than those in the non-variant group (p < 0.000). The conservative scores of those carrying the P/LP variant group were >7. C3, C3/C0, and C3/C2 values of newborns carrying VUS (c.1159A>C and c.1286A>G) were significantly higher than those of the non-variant group and the remaining VUS newborns (p < 0.005). The conservative scores of c.1159A>C and c.1286A>G calculated by ConSurf analysis were 9 and 7, respectively. Unfortunately, three MMA patients with c.1159A>C died during the neonatal period; their C3, C3/C0, C3/C2, and MMA levels were significantly higher than those of the controls. Common variants of methylmalonic acidemia in the study population were categorized as VUS. In the neonatal period, the metabolic biomarkers of those carrying the P/LP variant group of the MUT gene were significantly higher than those in the non-variant group. If the metabolic biomarkers of those carrying VUS are also significantly increased, combined with silico analysis the VUS may be elevated to a likely pathogenic variant. The results also suggest that mass spectrometry and silico analysis may be feasible screening methods for verifying the pathogenicity of VUS in other inherited metabolic diseases.

Biocatalyst mediated green approach for 1,8-dioxo-octahydroxanthenes: SCXRD, Hirshfeld analysis and DFT studies as inhibitors of HIV reverse transcriptase

AIDS, caused by human immunodeficiency virus (HIV) is persistent on being one among the deadliest disease of all time. It destroys the immune system of the body and there is currently no effective cure for this. In this regard, in continuation to our studies on green catalysts, more efficient, constructive, and environmentally sustainable protocols for the synthesis of xanthene and its derivatives as HIV Reverse Transcriptase inhibitors were developed with the use of biocatalyst via baker's yeast that explores a viable approach on expanding environmental challenges and enlightens the superiority and exclusivity of this protocol. The current approach manifests numerous notable advantages that include ease of preparation, handling and benignity of the catalyst, low cost, green reaction conditions, facile workup, excellent yields (87–96 %) with extreme purity. The title compounds were docked on the crystal structure of a catalytic complex of HIV-1 reverse transcriptase (PDB: 1RTD). The C-score values achieved in the range 6.68–3.05 suggest that docking analysis was propitious signifying the review of all the forces of interaction between the ligand and the protein. The crystal studies and DFT analysis of compound 3d correlate the optimized geometrical features with empirically accessible XRD data.

A comprehensive analysis of aroma quality and perception mechanism in ginger-infused stewed beef using instrumental analysis, sensory evaluation and molecular docking

The ginger-infused stewed beef exhibited a satisfactory odor in Chinese cooking meat. This study aimed to reveal its aroma quality and perception mechanism through electronic nose, sensory evaluation and gas chromatography–mass spectrometry (GC–MS), gas chromatography-ion mobility spectrometry (GC-IMS) coupled with chemometric methods and molecular docking. Sensory evaluation and electronic nose analysis indicated ginger could greatly modify aroma profile of beef. Most C6-C10 aldehydes significantly decreased and terpenes increased in ginger-infused stewed beef. Orthogonal partial least squares-discriminant analysis (OPLS-DA) found 7 key markers for distinguishing stewed beef with or without ginger. Ginger additions could reduce fatty acids consumption. Moreover, the key contributors of fatty, bloody, meaty, ginger and mint aroma attributes, namely (E)-2-octenal, 1-octen-3-ol, 2-acetylthiazole, zingiberene and γ-elemene, respectively, selected by partial least squares regression (PLSR) analysis were docked with the olfactory receptor. Hydrogen bonds and hydrophobic interactions were the main interaction forces between olfactory receptor and the five compounds.

Exploring the interface dynamics of emulsion gel via a novel non-destructive technique provides insights into the underlying mechanism of gel formation, water mobility, functionality and structural variations

Tri-frequency ultrasound (TFU) at 20-40-60 kHz was used to systematically examine the effects on the multi-scale network structure of an emulsion gel containing orange essential oil prepared with glycosylated whey protein (WP). Treatment intervals of pre-and-post 10, 20, and 30 min were utilized to evaluate the influence and interactions on functional (particle size, zeta-potential), rheological (storage modulus (G′) and loss modulus (G″), and oxidative stability (conjugated diene and peroxide value). The optimized tri-frequency pre- and post-treated sample demonstrated enhanced physical stability as compared to the un-treated sample, as evidenced by droplet size, (from 468.14 ± 0.56 to 214.21 ± 0.42 nm), ζ-Potential (mV) (from −29.67 ± 0.31 to −39.98 ± 1.42), and structural morphology. Structure analysis using FTIR that the aforementioned improvements were made possible through TFU enhanced hydrogen bonds, molecular arrangements with greater order, and improved intermolecular compatibility. XRD results showed gradual shift from 8.32° to 8.64° and from 19.2° to 19.5°, respectively. TFU post-treatment gels exhibited higher viscosity, more pronounced pseudoplastic behavior compare to pre-treatment, attributed to strong interaction forces and three-dimensional gel network. Our results provide valuable insights into the application of multi-frequency ultrasound as a promising technique for designing protein emulsion gels tailored for nutrient delivery systems.

ANN Enhanced Hybrid Force/Position Controller of Robot Manipulators for Fiber Placement

In practice, most industrial robot manipulators use PID (Proportional + Integral + Derivative) controllers, thanks to their simplicity and adequate performance under certain conditions. Normally, this type of controller has a good performance in tasks where the robot moves freely, performing movements without contact with its environment. However, complications arise in applications such as the AFP (Automated Fiber Placement) process, where a high degree of precision and repeatability is required in the control of parameters such as position and compression force for the production of composite parts. The control of these parameters is a major challenge in terms of quality and productivity of the final product, mainly due to the complex geometry of the part and the type of tooling with which the AFP system is equipped. In the last decades, several control system approaches have been proposed in the literature, such as classical, adaptive or sliding mode control theory based methodologies. Nevertheless, such strategies present difficulties to change their dynamics since their design consider only some set of disturbances. This article presents a novel intelligent type control algorithm based on back-propagation neural networks (BP-NNs) combined with classical PID/PI control schemes for force/position control in manipulator robots. The PID/PI controllers are responsible for the main control action, while the BP-NNs contributes with its ability to estimate and compensate online the dynamic variations of the AFP process. It is proven that the proposed control achieves both, stability in the Lyapunov sense for the desired interaction force between the end-effector and the environment, and position trajectory tracking for the robot tip in Cartesian space. The performance and efficiency of the proposed control is evaluated by numerical simulations in MATLAB-Simulink environment, obtaining as results that the errors for the desired force and the tracking of complex trajectories are reduced to a range below 5% in root mean square error (RMSE).

Surface Hydroxylation-Induced Electrostatic Forces Thicken Water Films on Quartz.

Aqueous films on mineral surfaces control the physical, chemical, and biological transport processes in the atmosphere, soil, and rocks. Despite the importance of thin films for various research and engineering fields, there are still unanswered questions regarding the roles of the different forces affecting the nature of water films. One of these, the focus of this study, is the development of abnormally thick water films on quartz surfaces. In this study, we developed a density-functional-theory-based model to describe the time-dependent evolution of water films and identify the governing forces responsible for thickening films. We simulated the diffusion of water vapor from ambient air toward mineral surfaces and the formation and thickening of water films at various relative humidity values. Our model predicts an abnormal water film thickness on a hydroxylated quartz surface compared to a surface free of hydroxylation, which explains experimental observations. We further used the model to understand the key interaction forces at different stages of water film formation and thickening. Our model suggests that the attractive hydrogen bonding and van der Waals forces initiate a seed layer of water, and the electrostatic forces, generated by the hydroxylated and thus charged surface, lead to the thickening of water films. This generalizable model can provide insights into the peculiarities of water film development on various mineral surfaces.

Single-Molecule Detection of the Encounter and Productive Electron Transfer Complexes of a Photosynthetic Reaction Center.

Small, diffusible redox proteins play an essential role in electron transfer (ET) in respiration and photosynthesis, sustaining life on Earth by shuttling electrons between membrane-bound complexes via finely tuned and reversible interactions. Ensemble kinetic studies show transient ET complexes form in two distinct stages: an "encounter" complex largely mediated by electrostatic interactions, which subsequently, through subtle reorganization of the binding interface, forms a "productive" ET complex stabilized by additional hydrophobic interactions around the redox-active cofactors. Here, using single-molecule force spectroscopy (SMFS) we dissected the transient ET complexes formed between the photosynthetic reaction center-light harvesting complex 1 (RC-LH1) of Rhodobacter sphaeroides and its native electron donor cytochrome c2 (cyt c2). Importantly, SMFS resolves the distribution of interaction forces into low (∼150 pN) and high (∼330 pN) components, with the former more susceptible to salt concentration and to alteration of key charged residues on the RC. Thus, the low force component is suggested to reflect the contribution of electrostatic interactions in forming the initial encounter complex, whereas the high force component reflects the additional stabilization provided by hydrophobic interactions to the productive ET complex. Employing molecular dynamics simulations, we resolve five intermediate states that comprise the encounter, productive ET and leaving complexes, predicting a weak interaction between cyt c2 and the LH1 ring near the RC-L subunit that could lie along the exit path for oxidized cyt c2. The multimodal nature of the interactions of ET complexes captured here may have wider implications for ET in all domains of life.

Study on the adsorption mechanism of fluorescent nano-tracer in sandstone core

Chemical tracer testing technology has increasingly become the preferred method for reservoir monitoring in oil fields due to its low cost and high efficiency. Understanding the migration behavior and adsorption mechanisms of chemical tracers in porous media is crucial for designing tracer injection processes and enhancing the accuracy of tracer test interpretation. This study employs an enhanced Stöber sol-gel method to synthesize fluorescent silica nanoparticles. After surface modification with the silane coupling agent γ-(methacryloyloxy) propyltrimethoxysilane (KH570) and doping with two fluorescent dyes, a multicolor fluorescent nano-tracer (PMFN) was synthesized. This study conducted dynamic and equilibrium adsorption experiments to investigate the adsorption behavior of PMFN on sandstone surfaces. To elucidate the adsorption mechanism of PMFN, we fitted the adsorption equilibrium experimental data using the Langmuir, Freundlich, and Temkin isothermal adsorption models. The adsorption kinetics were studied using the Lagergren, Elovich, and pseudo-first-order kinetic models. Additionally, we assessed the influence of ionic strength and particle size on the adsorption of PMFN by calculating the DLVO interaction forces between PMFN and the sandstone surface. The results showed that PMFN adsorption on sandstone primarily occurs in the pre-contact stage and is characterized by monolayer adsorption. When the ionic strength of the solution is 0.001 mol/L, the maximum repulsive energy barrier between PMFN and the sandstone surface hinders adsorption.

Synthesis of a novel flocculant with dimethylamino propylmethacrylamide and polyether and its flocculation performance

The widespread use of polymer flooding has resulted in a large number of produced liquids consisting of crude oil emulsions and oily wastewater. Efficient flocculants are required to treat these produced liquids till the oily wastewater satisfies the requirements for reinjection formation in order to maintain the regular manufacturing process. In this work, an unsaturated polyether macromonomer (PEP-30) was prepared by ring-opening polymerization using isobutenol as a starting material. Subsequently, a novel flocculant (PMAP) was obtained by copolymerization of dimethylamino propylmethacrylamide (DMAPMA) and PEP-30. For the produced liquids with different crude oil emulsion content, the oil removal rate of PMAP at a dosage of 150 mg/L was more than 75%, and the oil removal rate and versatility were better than those of conventional cationic flocculants. Furthermore, the findings of the flocculation mechanism investigation demonstrated that PMAP had a low interfacial elastic modulus and a large interfacial adsorption mass. Specifically, the optical tweezers were used to detect the interaction force between oil droplets. PMAP effectively strengthened the attraction between oil droplets, extending their duration in contact during flocculation and promoting their coalescence.

The Interaction and Lift-Off Forces of an Atomic Force Microscope Tip from Single Fibers Extracted from Protective Clothing Fabric.

The widespread use of engineered nanoparticles (ENPs) poses a potential health hazard to humans, especially to those involved in either nanoparticle manufacturing or the usage and assembly of a final product. In this study, we performed systematic force vs distance experiments (F(z)) using an atomic force microscope (AFM) on fibers commonly used in street clothing and protective laboratory clothing to better characterize the relevant interaction forces between engineered nanoparticles (ENPs) and the contacted fabric fibers. The intent of this study is to identify those factors that influence the interaction of ENPs with fabrics with an aim to improve the efficacy of protective clothing against ENP exposure and mitigate potential health risks. A ∼14 nm diameter AFM SiOx tip (with nanoscale radius of curvature) is considered as an effective oxide ENP. Features present (or absent) in a well-executed F(z) AFM experiment provide a fingerprint that distinguishes the relevant forces and interaction mechanisms in play. Measurements of F(z) as a function of relative humidity were also performed to assess the importance of thin surface water layers in binding nanometer-size oxide ENPs to a fabric fiber. The F(z) data indicate the dominant mechanism for adhesion of the oxide tip to the various fabric fibers (cotton, Tyvek (HD polyethylene), polypropylene, and polyester) can be attributed to a van der Waals interaction. The analysis provides no evidence for long-range electrostatic forces or capillary-induced adhesion of the AFM tip to the fibers studied.

Multiple Interaction Forces Construct Two‐Dimensional Self‐assembly Kagome Lattices on Au(111)

Comprehensive SummaryKagome lattices have garnered significant attention due to their promising applications in catalysis, electronics, and magnetics. Although many efforts have been paid to the design and synthesis of Kagome lattices, there is a limited focus on constructing this lattice by multiple interaction forces. In this work, we employ 2,7‐dibromo‐carbazole as precursors to successfully fabricate the two‐dimensional self‐assembly Kagome lattices stabled by multiple interaction forces on Au(111) substrate. Using low‐temperature scanning tunneling microscopy, non‐contact atomic force microscopy and density functional theory calculation, we visualize and identify the four interaction forces within Kagome lattices: Au—N coordination bonds, Au—H hydrogen bonds, Br—Br halogen bonds, and Br—H hydrogen bonds, respectively. This study provides a basic understanding for designing and constructing more complex Kagome lattices.

Dual-Responsive "Egg-Box" Shaped Microgel Beads Based on W1/O/W2 Double Emulsions for Colon-Targeted Delivery of Synbiotics.

In this study, for enhancing the resistance of probiotics to environmental factors, we designed a microgel beads delivery system loaded with synbiotics. Multiple droplets of W1/O/W2 emulsions stabilized with zein-apple pectin hybrid nanoparticles (ZAHPs) acted as the inner "egg," whereas a three-dimensional network of poly-L-lysine (PLL)-alginate-CaCl2 (Ca) crosslinked gel layers served as the outermost "box." ZAHPs with a mass ratio of 2:1 zein-to-apple pectin showed excellent wettability (three-phase contact angle = 89.88°). The results of the ζ-potentials and Fourier transform infrared spectroscopy demonstrate that electrostatic interaction forces and hydrogen bonding were the main forces involved in the formation of ZAHPs. On this basis, we prepared W1/O/W2 emulsions with other preparation parameters and observed their microstructures by optical microscopy and confocal laser scanning microscope. The multi-chambered structures of W1/O/W2 emulsions were successfully visualized. Finally, the W1/O/W2 emulsions were coated with PLL-alginate-Ca using the solution extrusion method. The results of the in vitro colonic digestion stage reveal that the survival rate of probiotics in the microgel beads was about 75.11%, which was significantly higher than that of the free. Moreover, probiotics encapsulated in microgel beads also showed positive storage stability. Apple pectin would serve as both an emulsifier and a prebiotic. Thus, the results indicate that the "egg-box" shaped microgel beads, designed on the basis of pH-sensitive and enzyme-triggered mechanisms, can enhance the efficiency of probiotics translocation in the digestive tract and mediate spatiotemporal controlled release.

Dependent Hidden Markov Model for pedestrian intention prediction: considering Multivariate Interaction Force

Accurately recognizing and predicting pedestrian intentions is crucial for autonomous vehicle safety. However, existing prediction models often fail to comprehensively consider interactions between various traffic elements, resulting in suboptimal accuracy and robustness, especially in complex environments. To address this, we propose a pedestrian intention prediction model combining the Multivariate Interaction Force (MIF) model and a Dependent Hidden Markov Model (DE-HMM) for unsignalized midblock crossings. The MIF model captures dynamic interactions among pedestrians, vehicles, and the environment, while DE-HMM uses MIF data and pedestrian head orientation for predictions. Our model achieves 91.5% accuracy in recognizing crossing intentions, and 88.7% and 85.1% accuracy for predictions 0.5s and 1s ahead, respectively, outperforming current mainstream models and demonstrating strong robustness in special scenarios.

Structural and computational insights into two completely unanticipated Cu(II) and Ni(II) complexes derived from a bifunctional salamo-type bis(pyridine)-arm ligand

A bifunctional Salamo-type bis(pyridine)-arm ligand H2L (4,4′-Methyl-6,6′-pyridinenitrilomethylidyne-2,2′-[ethylenedioxybis(nitrilomethylidyne)]diphenol) was designed and synthesized, which can react with Cu(II) and Ni(II) nitrates to hydrolyze & break the C = N double bonds of new ligand H2L′ (4,4′-Methyl-6,6′-formal-2,2′-[ethylenedioxybis(nitrilomethylidyne)]diphenol). The ligand reacted with Cu(II) and Ni(II) salts to form respectively complexes [Cu(L′)] (1) and [Ni2(L′)(H2O)2](NO3)2 (2). They were elucidated by single crystal X-ray method. Many important noncovalent interactions, such as intramolecular hydrogen bonding, intermolecular hydrogen bonding and π···π stacking interactions, can be observed in the crystal structures of the two complexes. IR & UV–Vis absorbent spectroscopic analysis showed that the ligand unit is involved in the coordination with copper(II) and nickel(II) atoms, and ultraviolet titration and fluorescence titration spectra verified that the coordinating radios of the two complexes formed in liquid phase are in accordance with those of single-crystal X-ray diffraction. Through DFT theoretical calculations and electrostatic potential analyses (MESP) of the ligand and its complexes, the configuration of the ligand at the lowest energy were deeply understood, and it was demonstrated that the coordination reaction at salamo sites requires a great torsional force, and the weak intermolecular interaction force and the energy gaps of HOMO-LUMO orbitals were profoundly discussed, and the Cu(II) and Ni(II) complexes exhibit anomalous fluorescence enhancement behaviors.

Effects of methanol and ethylene glycol on the interactions between methane hydrate particles and water droplets

Hydrate particle agglomeration is one of the main causes of hydrate blockage in pipelines. Although methanol (MeOH) and ethylene glycol (MeG) are the most used thermodynamic hydrate inhibitors, their effects on the micromechanics behavior of natural gas hydrate particle agglomeration are not clear. In this study, the effects of MeOH and MeG on the interaction force between methane hydrate particles and droplets were investigated using a self-built high-pressure hydrate microforce measuring device. The results suggest that, with the concentration increase from 1% to 7%, for the system with MeOH, the adhesion force reduced by 11% to 33%, while for MeG, the adhesion force reduced by 15% to 43%. On the one hand, the addition of inhibitors reduces the phase equilibrium temperature, which decreases the solidification rate of water in liquid bridge, and on the other hand, they reduce the interfacial tension. both reductions lead to lower adhesion force. Furthermore, in comparison with MeG, the MeOH solutions present a lower contact angle, resulting in a larger hydrate particle-droplet contact area and thus relatively higher adhesion force. The measurement and observation in the present work provide new insight into the mechanism of methanol and ethylene glycol on inhibiting hydrate agglomeration, which is important in advancing the management of hydrate formation in pipelines.

Building Functional Liquid‐Based Interfaces: From Mechanism to Application

AbstractFunctional liquid‐based interfaces, with their inhomogeneous regions that emphasize the functionalized liquids, have attracted much interest as a versatile platform for a broad spectrum of applications, from chemical manufacturing to practical uses. These interfaces leverage the physicochemical characteristics of liquids, alongside dynamic behaviors induced by macroscopic wettability and microscopic molecular exchange balance, to allow for tailored properties within their functional structures. In this Minireview, we provide a foundational overview of these functional interfaces, based on the structural investigations and molecular mechanisms of interaction forces that directly modulate functionalities. Then, we discuss design strategies that have been employed in recent applications, and the crucial aspects that require focus. Finally, we highlight the current challenges in functional liquid‐based interfaces and provide a perspective on future research directions.

Numerical method of lateral pipe-soil interaction and sensitivity analysis investigation

The pipe-soil interaction force is a crucial load that ensures the on-bottom stability of submarine pipelines and acts as a vital input parameter for the design of controlled pipeline buckling. It is necessary to precise prediction of soil lateral resistance and sensitivity to environmental parameters. This study developed a numerical simulation technique based on the coupled Euler-Lagrange (CEL) method to systematically analyse the deformation of the pipeline and the soil-pipeline forces on the seabed foundation during service. To validate the numerical method for large lateral displacement of pipe-soil interaction, an experimental approach employing parameter variation was utilized to conduct sensitivity analysis on the environmental parameters. The key parameters affecting soil-pipeline interaction were determined through an analysis of relative variation factors. The research findings demonstrate a satisfactory agreement, with an amplitude difference range of within 15 %, between the numerical simulation technique using the CEL method and the experimental results. This method resolves the issue of non-convergence due to grid distortion under conditions of large displacement, thereby enhancing computational accuracy. Sensitivity analysis shows that the relative variation factors for soil friction angle, initial burial depth, and soil density exceed 50 %, which is notably higher than the elastic modulus, friction coefficient, and Poisson's ratio of the soil. The results of this study enable the prediction of lateral forces in pipe-soil interaction and identification of environmentally sensitive parameters. This study establishes a foundation for calculating pipeline buckling strength in complex environments and holds paramount importance for the design and construction of pipelines to ensure on-bottom stability.

Superior energy storage performance achieved in tungsten bronze SBCN-based ceramics through tape-casting

Simultaneously integrating outstanding energy storage density and good energy storage efficiency in advanced ferroelectrics is crucial to implementing the application of dielectrics in high-power pulse devices. In this work, (Sr0.5Ba0.5)2Ca0.5Nb5-xSbxO15 ceramics were designed and prepared by adopting the B sites substitution engineering together with combining strategies of tape-casting method and two-step sintering process. Benefiting from the refined grain size and high density, the breakdown field of (Sr0.5Ba0.5)2Ca0.5Nb4.8Sb0.2O15 (SBCNS0.2) was promoted to 400 kV/cm. By the substitution of Sb5+ in the B sites, the weaker interaction force of Sb-O bond in BO6 octahedral polar unit induced the occurrence of polar nanoregions (PNRs) at room temperature to strengthen the dielectric relaxation behavior. Then it is noteworthy that SBCNS0.2 ceramics simultaneously obtained excellent recoverable energy density (Wrec, 3.9 J/cm3), energy storage efficiency (η, 90.5 %), power density (PD, 156.0 MW/cm3), and current density (CD, 1356.7 A/cm2). In addition, the SBCNS0.2 ceramics exhibited an ultrafast discharge time (t0.9, 67 ns). These results reveal prospective potential of unfilled tungsten bronze SBCNS0.2 ceramics in power capacitor applications and provide an effective strategy for improving excellent energy storage properties from the perspective of preparation methods.