Characteristics of the Boundary Layer Structure of Sea Fog on the Coast of Southern China

Using boundary layer data with regard to sea fog observed at the Science Experiment Base for Marine Meteorology at Bohe,Guangdong Province,the structure of the atmospheric boundary layer and the characteristics of the tops of the fog and the clouds were analyzed.In addition,the effects of advection,radiation,and turbulence during sea fog were also investigated.According to the stability definition of saturated,wet air,the gradient of the potential pseudo-equivalent temperature equal to zero was defined as the thermal turbulence interface.There is evidence to suggest that two layers of turbulence exist in sea fog.Thermal turbulence produced by long-wave radiation is prevalent above the thermal turbulence interface,whereas mechanical turbulence aroused by wind shear is predominant below the interface.The height of the thermal turbulence interface was observed between 180 m and 380 m.Three important factors are closely related to the development of the top of the sea fog：（1） the horizontal advection of the water vapor,（2） the long-wave radiation of the fog top,and（3） the movement of the vertical turbulence.Formation,development,and dissipation are the three possible phases of the evolution of the boundary-layer structure during the sea fog season.In addition,the thermal turbulence interface is the most significant turbulence interface during the formation and development periods;it is maintained after sea fog rises into the stratus layer.

Modifying element diffusion pathway by transition layer structure in high-entropy alloy particle reinforced Cu matrix composites

The Al0.3CoCrFeNi high-entropy alloy(HEA)particles reinforced Cu matrix composites(CMCs)were fabricated by mechanical alloying and sintering.Transition layer structure was obtained by multi-step ball milling to investigate the related influence on element diffusion behavior and wear properties of CMCs.The results indicate that a new Cu transition layer is generated,and the thickness is about 5μm.Cr element diffuses into the interface via the transition layer,which forms the complex oxide.Because of the structure of Cu transition layer,the diffusion rates of Ni,Co and Fe increase,especially the Ni element.The wear resistance of CMCs is improved by 30%,which is due to the improvement of interface bonding strength,compared with the CMCs without transition layer.This method is applicable to the development of advanced HEA reinforced metallic matrix composites.

Layer Structure Analysis of Low-Carbon Steel Containing Rare Earth by High-Temperature Carburizing of Liquid Cast-Iron

The layer structure of low-carbon steel containing RE by high-temperature (T>1200 ℃) carburizing of liquid cast-iron was studied and the diffusion activation energy of carbon was calculated by metallographic microscpe, chemical analysis etc. The result shows that the technology of carburizing in liquid cast-iron can expedite caburization distinctly and changes the carburizing layer structure. The carburizing rate is 60～80 times of that of the traditional technology, and there is about 43% decrease in the activation energy compared with gas-carburization. In outer structure layer, cementite is formed simultaneously both on the crystal boundary reticularly and inside the crystal grains stripedly. In inner carburizing layer, there is undissolved blocky ferrite in reticular cementite. Besides, rare earth element can expedite carburization process.

Synthesis and Microstructure of Partly-oriented Bismuth Layer Structure Ferroelectrics Ceramics SrBi_4Ti_4O_(15)

SrBi4Ti4O15 powder was synthesized by conventional solid state synthesis （ CS ） and molten salt synthesis （ MSS ） . MSS method can synthesize plate-like SrBi4Ti4O15 at lower temperature （900℃） than CS method. Plate-like form becomes more distinct when the synthesis temperature increases. This would help cause the grain orientation of the ceramics after sintering. The sintered samples of MSS had grain orientation at （0,0, 10） plane. The degree of （0,0,10） grain orientation F was 62.1% . Hot pressing made （0,0,10） grain orientation more distinct （ F = 85.7% ）. The microstructures of the sintered samples were detected by SEM. Due to the grain orientation the density of samples fabricated by MSS was lower than that of prepared by CS.

Weak Interactions and 2D Layer Structure of a New Ion-pair Complex Bis(1-benzyl-4-methylquinolinium)-bis(maleonitriledithiolato)nickel(Ⅱ)

A new ion-pair complex, [BzMeQ1]2[Ni（nmt）2]1（[BzMeQ1]^＋ = 1-benzyl-4-ntethylquino- linium, mnta- -- maleonitriledithiolate） has been synthesized and structurally characterized by IR, ESI-MS and X-ray diffraction methods. Complex 1 is of triclinic, space group PI, with a = 9.079（2）, b = 10.154（2）, c = 11.243（2）A, α= 81.58（1）, β= 69.63（1）, γ = 68.02（1）°, V= 940.1（3）A3, Dc = 1.427 g/cm^3, Z = 1, F（000） = 418 and R = 0.0442. A 2D layer structure is formed via the cation-cation π…π and C-H…π interactions observed in the solid state of the complex.

In-situ additive manufacturing of high strength yet ductility titanium composites with gradient layered structure using N_(2)

It has always been challenging work to reconcile the contradiction between the strength and plasticity of titanium materials.Laser powder bed fusion(LPBF) is a convenient method to fabricate innovative composites including those inspired by gradient layered materials.In this work,we used LPBF to selectively prepare Ti N/Ti gradient layered structure(GLSTi)composites by using different N_(2)–Ar ratios during the LPBF process.We systematically investigated the mechanisms of in-situ synthesis Ti N,high strength and ductility of GLSTi composites using microscopic analysis,TEM characterization,and tensile testing with digital image correlation.Besides,a digital correspondence was established between the N_(2) concentration and the volume fraction of LPBF in-situ synthesized Ti N.Our results show that the GLSTi composites exhibit superior mechanical properties compared to pure titanium fabricated by LPBF under pure Ar.Specifically,the tensile strength of GLSTi was more than 1.5times higher than that of LPBF-formed pure titanium,reaching up to 1100 MPa,while maintaining a high elongation at fracture of 17%.GLSTi breaks the bottleneck of high strength but low ductility exhibited by conventional nanoceramic particle-strengthened titanium matrix composites,and the hetero-deformation induced strengthening effect formed by the Ti N/Ti layered structure explained its strength-plasticity balanced principle.The microhardness exhibits a jagged variation of the relatively low hardness of 245 HV0.2 for the pure titanium layer and a high hardness of 408 HV0.2 for the N_(2) in-situ synthesis layer.Our study provides a new concept for the structure-performance digital customization of 3D-printed Ti-based composites.

Reversible Mn^(2+)/Mn^(4+)double-electron redox in P3-type layer-structured sodium-ion cathode

The balance between cationic redox and oxygen redox in layer-structured cathode materials is an important issue for sodium batteries to obtain high energy density and considerable cycle stability.Oxygen redox can contribute extra capacity to increase energy density,but results in lattice instability and capacity fading caused by lattice oxygen gliding and oxygen release.In this work,reversible Mn^(2+)/Mn^(4+)redox is realized in a P3-Na_(0.65)Li_(0.2)Co_(0.05)Mn_(0.75)O_(2)cathode material with high specific capacity and structure stability via Co substitution.The contribution of oxygen redox is suppressed significantly by reversible Mn^(2+)/Mn^(4+)redox without sacrificing capacity,thus reducing lattice oxygen release and improving the structure stability.Synchrotron X-ray techniques reveal that P3 phase is well maintained in a wide voltage window of 1.5-4.5 V vs.Na^(+)/Na even at 10 C and after long-term cycling.It is disclosed that charge compensation from Co/Mn-ions contributes to the voltage region below 4.2 V and O-ions contribute to the whole voltage range.The synergistic contributions of Mn^(2+)/Mn^(4+),Co^(2+)/Co^(3+),and O^(2-)/(O_n)^(2-)redox in P3-Na_(0.65)Li_(0.2)Co_(0.05)Mn_(0.75)O_(2)lead to a high reversible capacity of 215.0 m A h g^(-1)at 0.1 C with considerable cycle stability.The strategy opens up new opportunities for the design of high capacity cathode materials for rechargeable batteries.

Analysis of Boundary Layer Structure,Turbulence,and Flux Variations before and after the Passage of a Sea Breeze Front Using Meteorological Tower Data

A detailed analysis of a sea breeze front(SBF)that penetrated inland in the Beijing–Tianjin–Hebei urban agglomeration of China was conducted.We focused on the boundary layer structure,turbulence intensity,and fluxes before and after the SBF passed through two meteorological towers in the urban areas of Tianjin and Beijing,respectively.Significant changes in temperature,humidity,winds,CO_(2),and aerosol concentrations were observed as the SBF passed.Differences in these changes at the two towers mainly resulted from their distances from the ocean,boundary layer conditions,and background turbulences.As the SBF approached,a strong updraft appeared in the boundary layer,carrying near-surface aerosols aloft and forming the SBF head.This was followed by a broad downdraft,which destroyed the near-surface inversion layer and temporarily increased the surface air temperature at night.The feeder flow after the thermodynamic front was characterized by low-level jets horizontally,and downdrafts and occasional updrafts vertically.Turbulence increased significantly during the SBF’s passage,causing an increase in the standard deviation of wind components in speed.The increase in turbulence was more pronounced in a stable boundary layer compared to that in a convective boundary layer.The passage of the SBF generated more mechanical turbulences,as indicated by increased friction velocity and turbulent kinetic energy(TKE).The shear term in the TKE budget equation increased more significantly than the buoyancy term.The atmosphere shifted to a forced convective state after the SBF’s passage,with near isotropic turbulences and uniform mixing and diffusion of aerosols.Sensible heat fluxes(latent heat and CO_(2)fluxes)showed positive(negative)peaks after the SBF’s passage,primarily caused by horizontal and vertical transport of heat(water vapor and CO_(2))during its passage.This study enhances understanding of boundary layer changes,turbulences,and fluxes during the passage of SBFs over urban areas.

Layered Structural PBAT Composite Foams for Efficient Electromagnetic Interference Shielding

The utilization of eco-friendly,lightweight,high-efficiency and high-absorbing electromagnetic interference(EMI)shielding composites is imperative in light of the worldwide promotion of sustainable manufacturing.In this work,magnetic poly(butyleneadipate-coterephthalate)(PBAT)microspheres were firstly synthesized via phase separation method,then PBAT composite foams with layered structure was constructed through the supercritical carbon dioxide foaming and scraping techniques.The merits of integrating ferroferric oxideloaded multi-walled carbon nanotubes(Fe3O4@MWCNTs)nanoparticles,a microcellular framework,and a highly conductive silver layer have been judiciously orchestrated within this distinctive layered configuration.Microwaves are consumed throughout the process of“absorption-reflection-reabsorption”as much as possible,which greatly declines the secondary radiation pollution.The biodegradable PBAT composite foams achieved an EMI shielding effectiveness of up to 68 dB and an absorptivity of 77%,and authenticated favorable stabilization after the tape adhesion experiment.

Difficulties, strategies, and recent research and development of layered sodium transition metal oxide cathode materials for high-energy sodium-ion batteries

Energy-storage systems and their production have attracted significant interest for practical applications.Batteries are the foundation of sustainable energy sources for electric vehicles(EVs),portable electronic devices(PEDs),etc.In recent decades,Lithium-ion batteries(LIBs) have been extensively utilized in largescale energy storage devices owing to their long cycle life and high energy density.However,the high cost and limited availability of Li are the two main obstacles for LIBs.In this regard,sodium-ion batteries(SIBs) are attractive alternatives to LIBs for large-scale energy storage systems because of the abundance and low cost of sodium materials.Cathode is one of the most important components in the battery,which limits cost and performance of a battery.Among the classified cathode structures,layered structure materials have attracted attention because of their high ionic conductivity,fast diffusion rate,and high specific capacity.Here,we present a comprehensive review of the classification of layered structures and the preparation of layered materials.Furthermore,the review article discusses extensively about the issues of the layered materials,namely(1) electrochemical degradation,(2) irreversible structural changes,and(3) structural instability,and also it provides strategies to overcome the issues such as elemental phase composition,a small amount of elemental doping,structural design,and surface alteration for emerging SIBs.In addition,the article discusses about the recent research development on layered unary,binary,ternary,quaternary,quinary,and senary-based O3-and P2-type cathode materials for high-energy SIBs.This review article provides useful information for the development of high-energy layered sodium transition metal oxide P2 and O3-cathode materials for practical SIBs.

Tuning the layer structure of molybdenum trioxide towards high-performance aqueous zinc-ion batteries

Aqueous zinc-ion batteries(ZIBs) have attracted significant attentions because of low cost and high reliability. However, conventional ZIBs are severely limited by the development of high energy density cathode materials with reversible Zn^(2+)insertion/extraction. Herein, a conducting polymer intercalated MoO_(3)(PMO) with extensively extended interlayer spacing is developed as a high-performance ZIBs cathode material. The interlayer spacing of PMO is prominently increased which results in an improved Zn^(2+)mobility during charge and discharge process. More significantly, the electrochemical results reveals that the intercalation of PANI facilitates the charge storage and reinforces the layered structure of MoO_(3), leading to a high capacity and good cycling stability. DFT calculation further reveals the intercalation of PANI into MoO_(3)significantly lower Zn^(2+)diffusion barrier. Benefit from these advantages, the ZIBs based on PMO electrode delivers a considerable capacity of 157 m Ah/g at 0.5 A/g and ameliorative stability with 63.4%capacity retention after 1000 cycles.

LiZr_(2)(PO_(4))_(3)surface coating towards stable layer structure Li_(1.2)Mn_(0.54)Ni_(0.13)Co_(0.13)O_(2)cathode materials with long cycle performance

Li-rich manganese-based materials are considered to be the mainstream cathode materials for next-generation lithium-ion batteries due to high discharge capacity and low cost,but poor cycle life and high temperature performance limit their development.Herein,LiZr_(2)(PO_(4))_(3)(LZPO)is coated on the surface of spherical Li_(1.2)Mn_(0.54)Ni_(0.13)Co_(0.13)O_(2)(LMNCO)material by a simple wet chemical method.The LZPO layer not only has the function of traditional coating layer to inhibit the occurrence of side reactions between electrolyte and LMNCO surface but also promotes the formation of spinel phase in the layered structure,increases the content of lattice oxygen,and reduces the content of absorbed oxygen.Thus,LZPO coated LMNCO has a more stable layered structure during cycling compared pure LMNCO,which improves effectively its long life and high temperature performance.The capacity loss rate of LZPO coated LMNCO is only 16.2%and 11.9%after 350 cycles at 25℃and 200 cycles at 50℃,respectively.Moreover,the capacity retention rate of the full cell composed of LZPO coated LMNCO and graphite is 70.7%after 200 cycles at 1.0 C.The coating layer toward stable surface structure can provide an idea for the modification of cathode materials,especially for Li-rich manganese-based materials.

High-Throughput Growth of Hexagonal Boron Nitride Film Using Porous-Structure Isolation Layer

Chemical vapor deposition is considered as the most hopeful method for the synthesis of large-area high-quality hexagonal boron nitride on the substrate of catalytic metal. However, the size the hexagonal boron nitride films are limited to the size of growth chamber, which indicates a lower production efficiency. In this paper, the utilization efficiency of growth chamber is highly improved by alternately stacking multiple pieces of Cu foils and carbon fiber surface felt with porous structure. Uniform and continuous hexagonal boron nitride films are prepared on Cu foils through chemical vapor deposition utilizing ammonia borane as the precursor. This work develops a simple and practicable method for high-throughput preparation of hexagonal boron nitride films, which could contribute to the industrial application of hexagonal boron nitride. .

First-Principles Study of the New Layered Ternary Metal Telluride,Eu_(2)InTe_(5)

In this study,we performed first-principles calculations using the VASP(Vienna Ab initio Simulation)software package to investigate the crystal structure,electronic structure,and optical properties of a new layered ternary metal chalcogenide,Eu_(2)InTe_(5).Our results show that Eu_(2)InTe_(5) is a non-zero-gap metal with a layered structure characterized by strong intra-layer atomic bonding and weak inter-layer interaction,which suggests its potential application as a nanomaterial.We also studied the optical properties,including the absorption coefficient,imaginary and real parts of the complex dielectric constant,and found that Eu_(2)InTe_(5) exhibits strong photoresponse characteristics at the junction of ultraviolet and visible light as well as blue-green light,with peaks at wavelengths of 389 nm and 477 nm.This suggests that it could be used in the development of UV(ultraviolet)detectors and other optoelectronic devices.Furthermore,due to its strong absorption,low loss,and low reflectivity,Eu_(2)InTe_(5) has the potential to be used as a promising photovoltaic absorption layer in solar cells.

Quasi-periodic layer structure of die-upset NdFeB magnets

Isotropic magnets were prepared from melt-spun powders at different hot pressing temperatures from 550 to 700 ℃, then upset into fully dense anisotropic magnets at the same die-upsetting temperature of 850 ℃. Die-upset magnets had the characteristics of inhomogeneous microstructure, including well-aligned grains structure and nonaligned grains layers transverse to press direction, which was quasi-periodic layer structure with a total length of 5-15 μm. Nonaligned grains layers were mainly made of large grains and had higher Nd content. To clearly understand the formation of layer structure, the microstructure of isotropic precursors with different hot pressing temperatures and their subsequent die-upset magnets was investigated. A new interpretation for the formation of layer structure was proposed in this paper： the layer structure was correlated to the original ribbon interface which was divided into three types based on the contact forms. Because of the incomplete contact of neighboring ribbons, concentration of stress occurred in the contacted points and the Nd-rich phase was squeezed into interspaces at high temperature under stress. Due to the release of interfacial energy and the fluidity of enough Nd-rich liquid phases, the nonaligned layers with large grains formed both in hot compaction and subsequent hot deformation process. The layer structure affected the magnetic properties of die-upset magnets. With increase of the hot pressing temperature, the nonaligned grains layers became thicker, and the magnetic performance of die-upset magnets decreased. It was necessary to reduce the thickness of large grains layers for the preparation of high-performance die-upset magnets.

Analyses of structure of planetary boundary layer in ice camp over Arctic ocean

The vertical structure of Planetary boundary layer over Arctic floating ice is presented by using about 50 atmospheric profiles and relevant data sounded at an ice station over Arctic Ocean from 22 August to 3 September,2003.It shows that the height of the convective boundary layer in day is greater than that of the stability boundary layer in night.The boundary layer can be described as vertical structures of stability,instability and multipling The interaction between relative warm and wet down draft air from up level and cool air of surface layer is significant,which causes stronger wind shear,temperature and humidity inversion with typical wind shear of 10 m/s/100 m,intensity of temperature inversion of 8 ℃/100 m.While the larger pack ice is broken by such process,new ice free area in the high latitudes of arctic ocean.The interactions between air/ice/water are enhanced.The fact helps to understanding characteristics of atmospheric boundary layer and its effect in Arctic floating ice region.

Formation mechanism of periodic layered structure in Ni_3Si/Zn system

The formation of periodic layered structure in Ni3Si/Zn diffusion couples with Zn in vapor or liquid state was investigated by SEM-EDS, FESEM and XRD. The results show that the diffusion path in solid-liquid reaction is Ni3Si/（T＋γ）/γ/…T/γ/Ni4Zn12Si3/γ/…Ni4Zn12Si3/γ/Ni4Zn12Si3/δ…/Ni4Zn12Si3/δ/liquid-Zn, and the diffusion path in solid-vapor reaction is Ni3Si/θ/（T＋γ）/γ/…/T/γ/…T/γ/vapor-Zn. With increasing Zn diffusion flux, the diffusion reaction path moves toward the Zn-rich direction, and the distance from the Ni3Si substrate to the periodic layer pair nearest to the interface decreases. In the initial stage of both reactions,γphase nucleates and grows within T matrix phase at first, and then conjuncts together to form a band to reduce the surface energy. Based on the experimental results and diffusion kinetics analysis, the microstructure differences were compared and the formation mechanism of the periodic layered structure in Ni3Si/Zn system was discussed.

Characterization of cake layer structure on the microfiltration membrane permeability by iron pre-coagulation

A cake layer is formed by coagulation aggregates under certain transmembrane pressure in the coagulation-microfiltration （MF） process. The characteristics of humic acid aggregates coagulated by different iron-based coagulants, such as charge, size, fractal dimension and compressibility, have an effect on the cake layer structure. At the optimum iron dose of 0.6 to 0.8 mmol/L for ferric chloride （FC） and polymer ferric sulfate （PFS） pre-coagulation, at the point of charge neutralization for near zero zeta potential, the aggregate particles produced possess the greatest size and highest fractal dimension, which contributes to the cake layer being most loose with high porosity and low compressibility. Thus the membrane filterability is better. At a low or high iron dose of FC and PFS, a high negative or positive zeta potential with high charge repulsion results in so many small aggregate particles and low fractal dimension that the cake layer is compact with low porosity and high compressibility. Therefore the membrane fouling is accelerated and MF permeability becomes worse. The variation of cake layer structure as measured by scanning electric microscopy corresponds with the fact that the smaller the coagulation flocs size and fractal dimension are, the lower the porosity and the tighter the cake layer conformation. This also explains the MF membrane flux variation visually and accurately.

HRTEM Study of Three New Regularly Mixed-layer Structures of B_8S_6 Type in Ca-RE Fluorocarbonate Minerals

The microstructural features of clacium rare earth(Ca RE) fluorocarbonate minerals from Southwest China were studied by using selected area electron diffraction(SAED) and high resolution transmission electron microscopy(HRTEM). Three new regularly mixed layer structures of B 8S 6 type with long period and different stacking sequence, i.e. B 8S 6 Ⅰ, B 8S 6 Ⅱ, and B 8S 6 Ⅲ, were found in the derived polycrystal of parisite, in which their structural symmetry, cell parameters, chemical formulas of crystal and stacking models of structural unit layer, etc. were determined. The results of this study also show that these new regularly mixed layer structrues were formed by order stacking unit layer of bastnaesite(B) and synchisite(S) in varying proportion along c axis. The observation under HRTEM reveals that in the three new regularly mixed layer structures there are different distribution modes of Ce F ion layers, CO 2- 3 ion groups between the Ce F ion layers, and CO 2- 3 ion groups between Ce F and Ca 2+ ion layers, and there are some heterogeneous textures, such as disorder interlayer and stacking fault. It further proves the complexity of the crystal structure of the Ca RE fluorocarbonate minerals.

Structure and Properties of Mg-doped SrBi_4Ti_4O_(15) Bi-layered Compounds

The structure and properties of Mg-doped SrBi4Ti4O15（SBT） were dicussed. Mg substitution into SBT had two possibilities states with the dopant amount variety. Mg cation substituted mostly into Sr^2＋ and the amount proportion was 68.11%.Mg ion will substitute into Ti ion site in perovskite layer when the doping amount increases. Polarization increases sharply when x=0.1 and then decreases becauses of the domain pinning. The Curie temperature of Mg-doped SBT is about 300 ℃ and there is a broad diffuse phase transition near Tc with a flat peak near the Ta of SBT.