Planar Structure Research Articles

Experimental study on the dynamic mechanical and progressive fracture behavior of multi-jointed rock mass under repetitive impact loading

The failure of rock masses is often controlled by structural planes, and the study on the dynamic mechanical behavior of multi-jointed rock masses under repetitive dynamic loading is still few. A series of repetitive impact tests on multi-jointed gabbro (MJG) are conducted with the split Hopkinson pressure bar (SHPB) testing apparatus. The effects of repetitive impact and joint inclination angles (α) on the dynamic mechanical behavior of MJG from the perspectives of impact number, stress equilibrium, dynamic mechanical properties, energy evolution, and macro and micro failure modes are deeply investigated. The results show that the joint inclination angle affects the impact resistance of the MJG. Under repetitive impact loadings, the mechanical behavior of the MJG is consistent, with tensile wing cracks initiating from the joint tips and propagating along the loading direction until specimen failure. During this process, cracks propagate along the weakest paths, thereby consuming the energy generated by the impact and preventing the activation of other minor defects. The macroscopic failure of the MJG undergoes four stages: the appearance of white patch, crack coalescence, crack penetration, and fracture, with the final failure mode being splitting. The microscopic formation stage of white patch is divided into microcrack activation and microcrack widening.

Absorption by a Layered Microbolometer Pixel’s Active Element

Microbolometer arrays, i.e., arrays of micro-scale pixels sensing temperature via resistance changes, have proven to be an effective basis for real-time imaging instrumentation in infrared as well as terahertz frequencies. In previous work, a design of THz and IR absorbing nano-laminates of dielectric and metal layers was studied. It was shown via numerical modeling that absorption may be maximized by appropriate choices of thickness, permittivity and conductivity. In this work, an analytical approach to the problem is formulated based on the standard recursive multiple reflection formulas for multi-layered planar structures. The results fully confirm and extend previous numerical work. A previous relationship between wavelength and silicon thickness for maximum absorption, derived numerically for specific parameter combinations, is now generalized in a parametric closed form. The method can be extended to include multiple lossy dielectric layers and may serve as a tool for optimizing the absorption characteristics of more complex layered absorbing structures. This could enhance the sensitivity of the detection scheme of interest, providing benefits in terms of cost, efficiency, precision, and adjustability.

Unit‐Cell‐Thickness Electron Confinement by Geometrically Constrained Antipolar Ordering

AbstractAchieving precise electron or spin confinement is essential for the progress of oxide electronics and emerging quantum information processing. While 2D electron confinement is commonly achieved with bare surfaces, heteroepitaxial interfaces, and charged domain walls, its practical application poses challenges, notably by diverse confinement widths, limited material selection, and the lack of freedom of positioning to a desired location within a given material system. Here, with scrutinizing a novel defect structure, the study suggests a new strategy with compelling evidence to trigger electron confinement down to single unit‐cell‐thickness, through geometrically constrained antipolar ordering facilitated by superlattice‐like periodic planar faults in metallic SrFeO3. Employing atomic resolution electron microscopy and density functional theory, the results demonstrate that electrons are confined two‐dimensionally to screen the positive bound charges on head‐to‐head antipolar state boundary, meanwhile oxygen vacancies segregated in the planar faults compensate the negative bound charges on the tail‐to‐tail one, leading to the stabilization of the antipolar ordering. Additionally, distinguished from traditional methods, this approach offers a potential programing capability for achieving precise charge and spin control by regulating planar fault structure at atomic scale.

Enhancing mid-infrared surface phonon polariton modes: optimization of structural parameters in Nb-doped SrTiO3 with hole array structures for advanced infrared sensors

This study utilized the finite difference time domain method to investigate the mid infrared surface phonon polaritons and localized surface phonon resonances in undoped and niobium (Nb)-doped SrTiO3 (STO) with planar and holes array structures. Research has shown that Nb-doped STO operates in the Reststrahlen band of 8.06–18.48 µm, providing a wider spectral response than undoped STO (12.58–18.26 µm) and effectively covering the atmospheric window of long wave infrared. This indicates that the increase in virtual permittivity has the least impact on spectral broadening, indicating that the new infrared sensor technology has broad prospects. The optimization of structural parameters, including the period, filling factor, and depth of STO holes array, as well as the response to changes in incident light angle, is crucial for guiding the design of high-performance optoelectronic devices. In addition, this study explored the excitation of four resonant modes within a holes array and analyzed their relationship with array parameters to enhance the design of optoelectronic applications.

New lignans from Phyllanthodendron dunnianum

A new lignan phyllanins A (1) and a lignan phyllanins B (2) for which the absolute configuration was determined for the first time, along with four known lignans (3–6) were isolated from the branch and leaf extracts of Phyllanthodendron dunnianum. Their planar structures were mainly determined by a combination of 1D and 2D NMR, HRESIMS spectral analyses, and the absolute configurations of the compounds 1 and 2 were established by DFT GIAO 13C NMR and electronic circular dichroism (ECD) calculations. In addition, all these six lignans were firstly tested for the antibacterial activities against MRSA, Staphylococcus aureus, Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli. Among these compounds, 2 and 5 showed potential antibacterial activities against MRSA and S. aureus with MIC values of 4 and 8 µg/mL, respectively.

Experimental Study on the Influence of Structural Planes on Rockbursts in Deep-Buried Hard-Rock Tunnels

Experimental Study on the Influence of Structural Planes on Rockbursts in Deep-Buried Hard-Rock Tunnels

Three‐dimensional electrically conductive–hydrophobic layer for stable Zn metal anodes

AbstractThe interrelated side reactions and dendrites growth severely destabilize the electrode/electrolyte interfaces, resulting in the difficult application of aqueous Zn ion batteries (AZIBs). Hydrophobic protective layer possesses natural inhibition ability for side reactions. However, the conventional protective layer with plane structure is difficult to attain joint regulation of side reaction and Zn nucleation. Herein, a novel three‐dimensional (3D) electrically conductive and hydrophobic (3DECH) interface is elaborated to enable stable Zn anode. The as‐prepared 3DECH interface presents a uniform 3D morphology with hydrophobic property, large specific surface area, abundant zincophilic sites, and excellent electroconductivity. Therefore, the 3DECH interface achieves uniform nucleation and dendrite‐free deposition from synergetic benefits: (1) increased nucleation sites and reduced local current density through the special 3D structure and (2) uniform electric potential distribution and rapid Zn2+ transport due to the electroconductive alloy chemistry, thus coupling the hydrophobic property to obtain a highly reversible Zn anode. Consequently, the modified anode achieves a superior coulombic efficiency of 99.88% over 3500 cycles, and the pouch cells using modified anode and LiMn2O4 (LMO) cathode retain a capacity of 84 mAh g−1 after 700 cycles at a reasonable depth discharge of 36%, without dendrite piercing and “dead Zn.”

22]Pentaphyrins(2.0.1.1.0) Displaying N-Fusion, Pyrrole-Rearrangement, and Dimerization Reactions Upon Oxidation and Metalation.

Exploration of expanded porphyrins with unprecedented reactivities has remained important. Here [22]pentaphyrins(2.0.1.1.0) were synthesized as a constitutional isomer of sapphyrin by acid-catalyzed cyclization of 1,14-dibromo-5,10-diaryltripyrrin with 1,2-di(pyrro-2-ly)ethenes. These pentaphyrins display roughly planar structures and varying aromaticities depending upon the vinylene structures. The 19,20-ditolyl pentaphyrin gave an N-fused product and an unprecedented pyrrole-rearranged product, depending upon the oxidation conditions. Remarkably, upon the metalation with CuCl, the N-fused product and the pyrrole-rearranged product afforded an inner b-b coupled face-to-face CuII complex dimer and an outer b-b coupled lateral CuII complex dimer, respectively, in fairly good yields. Further, [22]pentaphyrin(2.0.1.1.0) fused with a NiII porphyrin was effectively dimerized upon oxidation with MnO2 to give a 16-16' directly linked dl-dimer.

22]Pentaphyrins(2.0.1.1.0) Displaying N‐Fusion, Pyrrole‐Rearrangement, and Dimerization Reactions Upon Oxidation and Metalation

Exploration of expanded porphyrins with unprecedented reactivities has remained important. Here [22]pentaphyrins(2.0.1.1.0) were synthesized as a constitutional isomer of sapphyrin by acid‐catalyzed cyclization of 1,14‐dibromo‐5,10‐diaryltripyrrin with 1,2‐di(pyrro‐2‐ly)ethenes. These pentaphyrins display roughly planar structures and varying aromaticities depending upon the vinylene structures. The 19,20‐ditolyl pentaphyrin gave an N‐fused product and an unprecedented pyrrole‐rearranged product, depending upon the oxidation conditions. Remarkably, upon the metalation with CuCl, the N‐fused product and the pyrrole‐rearranged product afforded an inner b‐b coupled face‐to‐face CuII complex dimer and an outer b‐b coupled lateral CuII complex dimer, respectively, in fairly good yields. Further, [22]pentaphyrin(2.0.1.1.0) fused with a NiII porphyrin was effectively dimerized upon oxidation with MnO2 to give a 16‐16’ directly linked dl‐dimer.

Paranazzamides A and B, new cyclic dipeptides containing a C7-prenylated tryptophan, produced by pathogenic reptile fungi Paranannizziopsis sp. UH-21.

Two new cyclic dipeptides, paranazzamides A (1) and B (2) containing a C7-prenylated tryptophan, were isolated from a culture broth of snake fungal disease-isolate Paranannizziopsis sp. UH-21. This is the first report on the new secondary metabolites from Paranannizziopsis sp. The planar structures of 1 and 2 were elucidated using various spectroscopic techniques including MS and 1D/2D NMR. The absolute configuration of 1 was assigned by comparison with the synthesized compound. Compounds 1 and 2 exhibited no antifungal activity, no antibacterial activity, and no cytotoxic activity even at a concentration of 128 µg ml-1, whereas 1 and 2 exhibited amphotericin B potentiating activity against Candida auris in combination treatment.

Size Control of Chiral Nanospheres Obtained via Nanoprecipitation of Helical Poly(phenylacetylene)s in the Absence of Surfactants.

Nanostructuration of dynamic helical polymers such as poly(phenylacetylene)s (PPAs) depends on the secondary structure adopted by the polymer and the functional group used to connect the chiral pendant to the PPA backbone. Thus, while PPAs with dynamic and flexible scaffolds (para- and meta-substituted, ω1< 165º) generate by nanoprecipitation low polydisperse nanospheres with controllable size at different acetone/water mixtures, those with a quasi-static behavior and the presence of an extended, almost planar structure (ortho-substituted, ω1> 165º), aggregate into a mixture of spherical and oval nanostructures whose size is not controlled. Photostability studies show that poly(phenylacetylene) particles are more stable to light irradiation than when dissolved macromolecularly. Moreover, the photostability of the particle depends on the secondary structure of the PPA and its screw sense excess. This fact, in combination with the encapsulation ability of these polymer particles, allows the creation of light stimuli-responsive nanocarriers, whose cargo can be delivered by light irradiation.

Size Control of Chiral Nanospheres Obtained via Nanoprecipitation of Helical Poly(phenylacetylene)s in the Absence of Surfactants

Nanostructuration of dynamic helical polymers such as poly(phenylacetylene)s (PPAs) depends on the secondary structure adopted by the polymer and the functional group used to connect the chiral pendant to the PPA backbone. Thus, while PPAs with dynamic and flexible scaffolds (para‐ and meta‐substituted, ω1&lt; 165º) generate by nanoprecipitation low polydisperse nanospheres with controllable size at different acetone/water mixtures, those with a quasi‐static behavior and the presence of an extended, almost planar structure (ortho‐substituted, ω1&gt; 165º), aggregate into a mixture of spherical and oval nanostructures whose size is not controlled. Photostability studies show that poly(phenylacetylene) particles are more stable to light irradiation than when dissolved macromolecularly. Moreover, the photostability of the particle depends on the secondary structure of the PPA and its screw sense excess. This fact, in combination with the encapsulation ability of these polymer particles, allows the creation of light stimuli‐responsive nanocarriers, whose cargo can be delivered by light irradiation.

Quinomycins with an unusual N-methyl-3-methylsulfinyl-alanine residue from a Streptomyces sp.

Four new echinomycin congeners, quinomycins M-P (1-4) were isolated from the cultures of the soil-derived Streptomyces sp. CPCC205575. The planar structures were determined by comprehensive analyses of NMR and HRESIMS/MS data. The absolute configurations were elucidated by the advanced Marfey's method combined with biosynthetic gene analysis. Compounds 1-4 represent the first examples of quinomycin-type natural products with the sulfur atom at the N,S-dimethylcysteine residue oxidized as a sulfoxide group forming the unusual N-methyl-3-methylsulfinyl-alanine residue. Bioassay results revealed that the oxidation of the sulfur atom at the Cys or Cys' residues led to dramatic decrease of cytotoxicity and antimicrobial activity.

Numerical and theoretical analysis of multi-pillar instability under elastic beams

With the increase of mining scale and depth, the cascading pillar failure (CPF) disaster has gradually become one of the core technical challenges for safe mining. This paper studies the CPF disaster of multi-pillar (P1-2, P2-3, P3-4 and P4-5) at 848 m level of Alhada Lead-Zinc Mine based on the RFPA2D numerical simulation software and stiffness theory. The numerical simulation results indicate that the load transfer effect induces the domino instabilities of double pillar (P2-3 and P3-4) and double pillar (P1-2 and P4-5), which is characterized by the ‘2 + 2’ compound failure mode. The physical essence of load transfer effect is revealed through numerical simulation, which is the elastic rebound of surrounding rockmass (such as roof-floor). In addition, the theoretical model of rebound overload mechanism of roof-multi-pillar-floor system is established based on the catastrophe theory, and the instability criterion, sudden jump and energy release of roof-multi-pillar-floor system are derived. Finally, the main influencing factors of load transfer effect such as pillar spacing and damage fracture zone are quantitatively analyzed, and the load transfer law shows that the load transfer effect decreases with the increasing pillar spacing and is hindered by the structural plane in the surrounding rockmass.

LCMS-Metabolomic Profiling and Genome Mining of Delftia lacustris DSM 21246 Revealed Lipophilic Delftibactin Metallophores.

Bacteria have evolved various strategies to combat heavy metal stress, including the secretion of small molecules, known as metallophores. These molecules hold a potential role in the mitigation of toxic metal contamination from the environment (bioremediation). Herein, we employed combined comparative metabolomic and genomic analyses to study the metallophores excreted by Delftia lacustris DSM 21246. LCMS-metabolomic analysis of this bacterium cultured under iron limitation led to a suite of lipophilic metallophores exclusively secreted in response to iron starvation. Additionally, we conducted genome sequencing of the DSM 21246 strain using nanopore sequencing technology and employed antiSMASH to mine the genome, leading to the identification of a biosynthetic gene cluster (BGC) matching the known BGC responsible for delftibactin A production. The isolated suite of amphiphilic metallophores, termed delftibactins C-F (1-4), was characterized using various chromatographic, spectroscopic, and bioinformatic techniques. The planar structure of these compounds was elucidated through 1D and 2D NMR analyses, as well as LCMS/MS-based fragmentation studies. Notably, their structures differed from previously known delftibactins due to the presence of a lipid tail. Marfey's and bioinformatic analyses were employed to determine the absolute configuration of the peptide scaffold. Delftibactin A, a previously identified metallophore, has exhibited a gold biomineralizing property; compound 1 was tested for and also demonstrated this property.

Influence of Weak Dynamic Disturbances on Rockburst Occurring in the Borehole Containing a Small-Scale Single Structural Plane: An Experimental Study

Influence of Weak Dynamic Disturbances on Rockburst Occurring in the Borehole Containing a Small-Scale Single Structural Plane: An Experimental Study

Recycling of waste coffee grounds as a photothermal material modified with ZnCl2 for water purification

The aim of this study was to develop a photothermal material modified with carbonization and ZnCl2 impregnation and supported by polyvinyl alcohol (PVA) for water purification using the waste coffee grounds. Scanning electron microscopy (SEM) characterization of the prepared material revealed that a significant surface modification was achieved due to the carbonization and ZnCl2 impregnation. X-ray diffraction analysis (XRD) pattern of the samples showed two broad peaks at 18.4° and 22.2°, this is due to the crystal planes of β-crystal phase structure, which indicates the existence of strong hydrogen bonds between the micro-structures and therefore less suspectable to chemical attack. Additionally, thermogravimetric analysis (TGA) result suggests a slight mass reduction between the temperature range of 65–75 °C implying the thermal stability of the prepared material. The produced modified material had a photothermal conversion efficiency of 74% and could produce vapor at a rate of 1.12 kg/m2h under 980 W/m2 irradiation at 1 sun. A significant reduction in Cu2+ ion concentration (83%), turbidity (91%), total dissolved solids (TDS) (61%), microbial load (95.6%), and total hardness (41.2%) were achieved. Therefore, waste coffee grounds can be considered as a future eco-friendly and low-cost candidate for water purification.

Dual-Polarization Conversion and Coding Metasurface for Wideband Radar Cross-Section Reduction

Modern stealth application systems require integrated meta-devices to operate effectively and have gained significant attention recently. This research paper proposes a 1-bit coding metasurface (CM) design. The fundamental component of the proposed CM is integrated to convert linearly polarized incoming electromagnetic waves into their orthogonal counterpart within frequency bands of 12.37–13.03 GHz and 18.96–32.37 GHz, achieving a polarization conversion ratio exceeding 99%. Furthermore, it enables linear-to-circular polarization conversion from 11.80 to 12.29, 13.17 to 18.44, and 33.33 to 40.35 GHz. A second element is produced by rotating a fundamental component by 90°, introducing a phase difference of π (pi) between them. Both elements are arranged in an array using a random aperiodic coding sequence to create a 1-bit CM for reducing the radar cross-section (RCS). The planar structure achieved over 10 dB RCS reduction for polarized waves in the frequency bands of 13.1–13.8 GHz and 20.4–30.9 GHz. A prototype was fabricated and tested, with the experimental results showing a good agreement with the simulated outcomes. The proposed design holds potential applications in radar systems, reflector antennas, stealth technologies, and satellite communication.

(C8H7N2O2)2[Bi2Br8]·2H2O and (C8H7N2O2)6[Bi2Cl10]Cl2·2H2O: Exploring Birefringent Crystals in Hybrid Halide Systems.

In this study, new hybrid birefringent crystals of (C8H7N2O2)2[Bi2Br8]·2H2O and (C8H7N2O2)6[Bi2Cl10]Cl2·2H2O were successfully synthesized by introducing a new birefringent group [C8H7N2O2]+ by a simple aqueous solution evaporation method. They crystallize in the P21/n space group, and their structure consists mainly of the π-conjugated group [C8H7N2O2]+ and the octahedron centered on Bi3+. By first-principles calculations, the birefringence response comes from the [C8H7N2O2]+ group with a planar π-conjugated structure. Meanwhile, the synthesis, structure, first-principles calculations, and optical properties are reported in this paper.

Tetrathiafulvalene carboxylate-based anode material for high-performance sodium-ion batteries.

Organic electrode materials are promising to be applied in sodium ion batteries (SIBs) due to their low cost and easily modified molecular structures. Nevertheless, low conductivity and high solubility in electrolytes still limit the development of organic electrodes. In this work, a carboxylate small molecule (BDTTS) based on tetrathiafulvalene is developed as anode material for SIBs. BDTTS has a large rigid π-conjugated planar structure, which may reduce solubility in the electrolyte, meanwhile facilitating charge transporting. Experimental results and theoretical calculations both support that apart from the four carbonyl groups, the sulfur atoms on tetrathiafulvalene also provide additional active sites during the discharge/charge process. Therefore, the additional active sites can well compensate for the capacity loss caused by the large molecular weight. The as-synthesized BDTTS electrode renders an excellent capacity of 230 mAh g-1 at a current density of 50 mA g-1 and an excellent long-life performance of 128 mAh g-1 at 2C after 500 cycles. This work enriches the study on organic electrodes for high-performance SIBs and paves the way for further development and utilization of organic electrodes.