Micropores in G20Mn5N cast steel and their influence on stress distribution

To accurately analyze the impact of casting pores in steel,high-resolution 3D X-ray tomography technology was used to gather detailed statistical information about micropores.These micropores were classified as gas,shrinkage,and gas-shrinkage pores depending on their formation origin and morphology.Clustering tendencies and affinity parameters were defined to characterize the spatial correlations among these three types of pores.The 3D data from X-ray tomography scans were then integrated into finite element analysis(FEA)software to predict how micropore shape,size,and distribution influence stress distribution within the material.The results show that certain inflection points with small local radii within the cast pores are major contributors to stress concentration.Therefore,cast pores cannot be simply modeled as ideal spherical pores.The sphericity and volume of pores have a significant impact on the stress concentration of the model.Specifically,lower sphericity and larger pore volumes result in higher stress concentrations.Moreover,the internal pores of steel castings exhibit specific global distribution characteristics.Pores located on the surface of the specimen lead to significantly higher stress concentrations compared to those located inside the specimen.

Comparative Analysis of Statistical Thickness Models for the Determination of the External Specific Surface and the Surface of the Micropores of Materials: The Case of a Clay Concrete Stabilized Using Sugar Cane Molasses

In this work, four empirical models of statistical thickness, namely the models of Harkins and Jura, Hasley, Carbon Black and Jaroniec, were compared in order to determine the textural properties (external surface and surface of micropores) of a clay concrete without molasses and clay concretes stabilized with 8%, 12% and 16% molasses. The results obtained show that Hasley’s model can be used to obtain the external surfaces. However, it does not allow the surface of the micropores to be obtained, and is not suitable for the case of simple clay concrete (without molasses) and for clay concretes stabilized with molasses. The Carbon Black, Jaroniec and Harkins and Jura models can be used for clay concrete and stabilized clay concrete. However, the Carbon Black model is the most relevant for clay concrete and the Harkins and Jura model is for molasses-stabilized clay concrete. These last two models augur well for future research.

A Model of Steady-State Convective Combustion of Micropore Propellants

Aim To develop a physical and mathematical model related to micropore para- meters of steady-state convective combustion of micropore propellants(MPP). Methods The micropore parameters were measured by WXT-88 mage analysis apparatus and the convective combustion characteristic of MPP was measured by a large volume closed bomb, respectively. Rasults Statistical physical model of burning in the micropore and granular burning were developed. The burning rate equation of steady-state convective combustion of MPP was obtained. Conclusions This model correlates the convective burning rate with micropores para- meters for the first time,and the calculating values of convective burning rate are in agreement with test results.The model also can be used to estimate the effects of microporous parame- ters, basic mass burning rate, MPP density and pressure in combustion chamber on the convective combustion characteristics of MPP.

Characterizing the Micropores in Lacustrine Shales of the Late Cretaceous Qingshankou Formation of Southern Songliao Basin, NE China

Micropores of shale are significant to the gas content and production potential of shale, which has been verified in the research of marine shale gas; while, few studies have been conducted on lacustrine shales. This study collected 42 samples from three wells in the Late Cretaceous Qingshankou Formation of the southern Songliao Basin, NE China, and investigated these samples by the focused ion beam-scanning electron microscope(FIB–SEM) and nitrogen adsorption analysis techniques. Four types of micropores were identified in the samples, i.e., intergranular pore, intracellular pore, organic matter pore and microfracture. The pore structure type is characterized by open slit pores and "ink type" pores which are mainly 1.5–5 nm in diameter with mesopores as the main pores. The mesopores account for 74.01% of the pore volume and 54.68% of the pore surface area. Compared with the lacustrine shales from the Triassic Yanchang Formation in the Ordos Basin and Xujiahe Formation in the Sichuan Basin, the intergranular clay mineral interlayer pores are considered to be the main reservoir space for shale gas storage in the study area, followed by intraparticle pores, organic matter pores and microfractures. Maturity and micropore are the key controlling factors which affect the shale gas content of the Qingshankou Formation in southern Songliao Basin.

Micropores regulating enables advanced carbon sphere catalyst for Zn-air batteries

Energy conversion technologies like fuel cells and metal-air batteries require oxygen reduction reaction(ORR)electrocatalysts with low cost and high catalytic activity.Herein,N-doped carbon spheres(N-CS)with rich micropore structure have been synthesized by a facile two-step method,which includes the polymerization of pyrrole and formaldehyde and followed by a facile pyrolysis process.During the preparation,zinc chloride(ZnCl2)was utilized as a catalyst to promote polymerization and provide a hypersaline environment.In addition,the morphology,defect content and activity area of the resultant N-CS catalysts could be regulated by controlling the content of ZnCl2.The optimum N-CS-1 catalyst demonstrated much better catalytic activity and durability towards ORR in alkaline conditions than commercial 20 wt%Pt/C catalysts,of which the half-wave potential reached 0.844 V vs.RHE.When applied in the Zn-air batteries as cathode catalysts,N-CS-1 showed a maximum power density of 175 mW cm^(-2) and long-term discharging stability of over 150 h at 10 mA cm^(-2),which outperformed 20 wt%Pt/C.The excellent performance could be due to its ultrahigh specific surface area of 1757 m2 g
1 and rich micropore channels structure.Meanwhile,this work provides an efficient method to synthesize an ultrahigh surface porous carbon material,especially for catalyst application.

A Universal Strategy For N-Doped 2D Carbon Nanosheets With Sub-Nanometer Micropore For High-Performance Supercapacitor

Preparing carbon nanosheets with precise control of open porous morphology via universal process and understanding the relationship between structure and capacitive performance are very urgent for achieving advanced supercapacitors.Herein,we propose a simple yet effective additive-free method to transform a bulk layered potassium phthalimide salt to novel nitrogen-doped twodimensional carbon sheets by self-activation during calcination.The obtained samples showed large-sized and flat structure with lateral size around 10μm,uniform sub-nanometer micropore size distribution of about 0.65 nm dimension,large specific surface area up to 2276.7 m^(2)g^(-1),and suitable nitrogen doping.Benefited from these merits,the optimized sample delivers a high specific capacitance of 345 F g^(-1)at 1 A g^(-1)and retains 270 F g^(-1)even at 50 A g^(-1)in6.0 M KOH electrolyte.Remarkably,the symmetric supercapacitor shows maximum energy densities of 16.43 Wh kg^(-1)and 23.6 Wh kg^(-1)in 6.0 M KOH and 1.0 M Na_(2)SO_(4)electrolytes,respectively.Importantly,on account the universality and simplicity of this method,the undoped as-prepared carbon sheet with uniform sub-nanometer micropore distribution can be synthesized from different potassium-containing salts with layered structure,which can be employed as a model for a deep understanding the effect of sub-nanometer micropores on capacitive performances.We find the number of micropores centered at 0.65 nm can be applied as one indicator to clarify the correlation between capacitance and critical pore size below 1 nm.

The nonlinear propagation of acoustic waves in a viscoelastic medium containing cylindrical micropores

Based on an equivalent medium approach, this paper presents a model describing the nonlinear propagation of acoustic waves in a viscoelastic medium containing cylindrical micropores. The influences of pores＇ nonlinear oscillations on sound attenuation, sound dispersion and an equivalent acoustic nonlinearity parameter are discussed. The calculated results show that the attenuation increases with an increasing volume fraction of micropores. The peak of sound velocity and attenuation occurs at the resonant frequency of the micropores while the peak of the equivalent acoustic nonlinearity parameter occurs at the half of the resonant frequency of the micropores. Furthermore, multiple scattering has been taken into account, which leads to a modification to the effective wave number in the equivalent medium approach. We find that these linear and nonlinear acoustic parameters need to be corrected when the volume fraction of micropores is larger than 0.1%.

CONCENTRATION PARTITION OF PROTEIN SOLUTION IN A MICROPORE:EFFECT OF ELECTROSTATIC INTERACTION

A theory for calculating the electrostatic interaction between protein molecules and the wallof a liquid-filled micropore is established in terms of solving the Laplace and the linearPoisson-Boltzmann equations.The surface charge of protein molecules is measured by theelectrophoresis velocity,whilethe charge of the pore wall is obtained by the ionic Donnan equilibrium.The theory is then used to study the influence of solute-pore electrostatic interaction on theconcentration partition of protein solution in a micropore under different solution properties.Experi-mental verification is performed by detecting the hindered diffusion of bovine serum albumin in thetrack-etched polycarbonate membranes.A good consistence between the theoretical and experimentaldata is being achieved.

Growth of Casting Microcrack and Micropore in Single-crystal Superalloys Analysed by Three-Dimensional Unit Cell

Finite element （FE） analysis was employed to investigate the casting microcrack and micropore growth in nickel-base single-crystal superalloys DD3. Based on the finite deformation rate-dependent crystallographic constitutive equation, the simulations of casting microcrack and micropore growth in three-dimensional unit cell model were carried out in a range of parameters including stress triaxiality, Lode parameter and type of activated slip systems. The FE results show that the stress triaxiality has profound effects on growth behavior, and the Lode parameter is also important for the casting microcrack and micropore growth. The type of operative slip systems has remarkable effect on casting microcrack and micropore growth, so the life of single- crystal component is associated with the type of activated slip systems, which is related to Schmid factor and the number of activated slip systems. The growth comparison between microcrack and micropore reveals that when the material is subjected to large deformation, the growth rate of microcrack is faster than that of micropore, i.e. microcrack is more dangerous than micropore; the microcrack is easier to result in brittle fracture than micropore. The stress triaxiality and Lode parameter have strong influence on the growth of microcrack and micropore.

Characterization of cellulose acetate micropore membrane immobilized acylase Ⅰ

This paper describes an innovative method for the immobilization of acylase I, which was entrapped into the CA-CTA micropore membrane. The most suitable casting solutions proportion for immobilizing the enzyme was obtained through orthogonal experiment. Properties of the enzyme membrane were investigated and compared with those of free enzyme and blank membrane. The thermal stability and pH stability of the enzyme inside the membrane were changed by immobilization. The optimum pH was found to be 6.0, which changes 1.0 unit compared with that of free acylase I. The optimum temperature was found to be about 90℃, which is higher than that of free acylase I (60℃). Experimental results showed that immobilization had effects on the kinetic parameters of acylase I.

Effect of Thermal Treatment of the Hydroxyapatite Powders on the Micropore and Microstructure of Porous Biphasic Calcium Phosphate Composite Granules

The effect of thermal treatment of the hydroxyapatite powders on the micropore structure of porous biphasic calcium phosphate (BCP) granules was examined. The porous BCP granules could be attained through mixing and sintering/fracturing thermally treated 60 wt% hydroxyapatite powders and calcined 40 wt% β-tricalcium phosphate powders. The observed Scanning electron microscopy (SEM) morphologies showed that the density of micropores (0.1 - 2.0 μm) including interconnected micropores of the porous BCP granules mixed with hydroxyapatite powders thermally treated at 900°C was significantly improved and the composite particles of porous BCP granules were homogeneously mixed and distributed. This result indicates that the particles of hydroxyapatite powders that have a tendency to agglomerate at a room temperature were well isolated and dispersed through thermal treatment processing before mixing with calcined β-tricalcium phosphate powders. The microstructural characterizations such as phase purity and composition of porous BCP granules were performed and verified by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) analysis.

The Soft X-ray Imager(SXI)on the SMILE Mission

The Soft X-ray Imager(SXI)is part of the scientific payload of the Solar wind Magnetosphere Ionosphere Link Explorer(SMILE)mission.SMILE is a joint science mission between the European Space Agency(ESA)and the Chinese Academy of Sciences(CAS)and is due for launch in 2025.SXI is a compact X-ray telescope with a wide field-of-view(FOV)capable of encompassing large portions of Earth’s magnetosphere from the vantage point of the SMILE orbit.SXI is sensitive to the soft X-rays produced by the Solar Wind Charge eXchange(SWCX)process produced when heavy ions of solar wind origin interact with neutral particles in Earth’s exosphere.SWCX provides a mechanism for boundary detection within the magnetosphere,such as the position of Earth’s magnetopause,because the solar wind heavy ions have a very low density in regions of closed magnetic field lines.The sensitivity of the SXI is such that it can potentially track movements of the magnetopause on timescales of a few minutes and the orbit of SMILE will enable such movements to be tracked for segments lasting many hours.SXI is led by the University of Leicester in the United Kingdom(UK)with collaborating organisations on hardware,software and science support within the UK,Europe,China and the United States.

Study on the evolution of solid–liquid–gas in multi-scale pore methane in tectonic coal

The rich accumulation of methane(CH_(4))in tectonic coal layers poses a significant obstacle to the safe and efficient extraction of coal seams and coalbed methane.Tectonic coal samples from three geologically complex regions were selected,and the main results obtained by using a variety of research tools,such as physical tests,theoretical analyses,and numerical simulations,are as follows:22.4–62.5 nm is the joint segment of pore volume,and 26.7–100.7 nm is the joint segment of pore specific surface area.In the dynamic gas production process of tectonic coal pore structure,the adsorption method of methane molecules is“solid–liquid adsorption is the mainstay,and solid–gas adsorption coexists”.Methane stored in micropores with a pore size smaller than the jointed range is defined as solid-state pores.Pores within the jointed range,which transition from micropore filling to surface adsorption,are defined as gaseous pores.Pores outside the jointed range,where solid–liquid adsorption occurs,are defined as liquid pores.The evolution of pore structure affects the methane adsorption mode,which provides basic theoretical guidance for the development of coal seam resources.

Effect of carbon material and surfactant on ink property and resulting surface cracks of fuel-cell microporous layers

Ensuring the consistency of electrode structure in proton-exchange-membrane fuel cells is highly desired yet challenging because of wide-existing and unguided cracks in the microporous layer(MPL). The first thing is to evaluate the homogeneity of MPL with cracks quantitatively. This paper proposes the homogeneity index of a full-scale MPL with an area of 50 cm~2, which is yet to be reported in the literature to our knowledge. Besides, the effects of the carbon material and surfactant on the ink and resulting MPL structure have been studied. The ink with a high network development degree produces an MPL with low crack density, but the ink with high PDI produces an MPL with low crack homogeneity. The polarity of the surfactant and the non-polarity of polytetrafluoroethylene(PTFE) are not mutually soluble,resulting in the heterogeneous PTFE distribution. The findings of this study provide guidelines for MPL fabrication.

Conjugated microporous polymers-scaffolded enzyme cascade systems with enhanced catalytic activity

Enhancing catalytic activity of multi-enzyme in vitro through substrate channeling effect is promis-ing yet challenging.Herein,conjugated microporous polymers(CMPs)-scaffolded integrated en-zyme cascade systems(I-ECSs)are constructed through co-entrapping glucose oxidase(GOx)and horseradish peroxidase(HRP),in which hydrogen peroxide(H_(2)O_(2)) is the intermediate product.The interplay of low-resistance mass transfer pathway and appropriate pore wall-H_(2)O_(2) interactions facilitates the directed transfer of H_(2)O_(2),resulting in 2.4-fold and 5.0-fold elevation in catalytic activ-ity compared to free ECSs and separated ECSs,respectively.The substrate channeling effect could be regulated by altering the mass ratio of GOx to HRP.Besides,I-ECSs demonstrate excellent stabili-ties in harsh environments and multiple recycling.

Insights into the Organotemplate-Free Synthesis of Zeolite Catalysts

As the most important nanoporous material, zeolites, which have intricate micropores, are essential heterogeneous catalysts in industrial processes. Zeolites are generally synthesized with organic templates under hydrothermal conditions; however, this method is environmentally unfriendly and costly due to the formation of harmful gases and polluted water. This article briefly summarizes the role of organic templates and describes designed routes for the organotemplate-free synthesis of zeolites, aided by zeolite seeds and zeolite seeds solution. Furthermore, this review explicates that the micmpore volume decreases with an increase of the Si/Al ratios in the organotemplate-free synthesis of zeolite products, where Na^＋ exists as an alkali cation. This feature is very important in directing the synthesis of zeolite catalysts with controllable Si/AI ratios under organotemplate-free conditions, and is thus important for the efficient design of zeolites.

Particle Size Distribution and Characterization of High Siliceous and Microporous Materials

Particle size, textural and surface characteristics influence some major technological properties of high siliceous aluminosilicate zeolite and sillicoaluminophosphate （SAPO） microporous materials. A comparative study was furnished for measuring surface characteristics, particle size and particle size distribution using particle size analyzer （PSA） and scanning electron microscope （SEM）. The PSA is capable of measuring particle diameter in micron range. The results of these techniques for estimation of particle size were compared and correlated statistically. Student t-test and variance ratio test （F-test） methods were performed for the significance of results by the analysis of variance （ANONA） and multiple-range tests. Textural and surface characteristics were evaluated by Brunauer, Emmett ＆ Teller （BET） volumetric technique and v-αs plotting method. The textural results shows that the external surface area and micropore volume of microporous materials were higher than those of the high siliceous zeolites and its zeotype materials.

Metal-organic frameworks MOF-808-X as highly efficient catalysts for direct synthesis of dimethyl carbonate from CO_2 and methanol

A series of metal-organic frameworks MOF-808-X(6-connected)were synthesized by regulating the ZrOCl2·8H2O/1,3,5-benzenetricarboxylic acid(BTC)molar ratio(X)and tested for the direct synthesis of dimethyl carbonate(DMC)from CO2 and CH3OH with 1,1,1-trimethoxymethane(TMM)as a dehydrating agent.The effect of the ZrOCl2·8H2O/BTC molar ratio on the physicochemical properties and catalytic performance of MOF-808-X was investigated.Results showed that a proper ZrOCl2·8H2O/BTC molar ratio during MOF-808-X synthesis was fairly important to reduce the redundant BTC or zirconium clusters trapped in the micropores of MOF-808-X.MOF-808-4,with almost no redundant BTC or zirconium clusters trapped in the micropores,exhibited the largest surface area,micropore size,and the number of acidic-basic sites,and consequently showed the best activity among all MOF-808-X,with the highest DMC yield of 21.5% under the optimal reaction conditions.Moreover,benefiting from the larger micropore size,MOF-808-4 outperformed our previously reported UiO-66-24(12-connected),which had even more acidic-basic sites and larger surface area than MOF-808-4,mainly because the larger micropore size of MOF-808-4 provided higher accessibility for the reactant to the active sites located in the micropores.Furthermore,a possible reaction mechanism over MOF-808-4 was proposed based on the in situ FT-IR results.The effects of different reaction parameters on DMC formation and the reusability of MOF-808-X were also studied.

A Fe-N-C catalyst with highly dispersed iron in carbon for oxygen reduction reaction and its application in direct methanol fuel cells

Exploring non‐precious metal catalysts for the oxygen reduction reaction （ORR） is essential for fuel cells and metal–air batteries. Herein, we report a Fe‐N‐C catalyst possessing a high specific surface area （1501 m2/g） and uniformly dispersed iron within a carbon matrix prepared via a two‐step pyrolysis process. The Fe‐N‐C catalyst exhibits excellent ORR activity in 0.1 mol/L NaOH electrolyte （onset potential, Eo=1.08 V and half wave potential, E1/2=0.88 V vs. reversible hydrogen electrode） and 0.1 mol/L HClO4 electrolyte （Eo=0.85 V and E1/2=0.75 V vs. reversible hydrogen electrode）. The direct methanol fuel cells employing Fe‐N‐C as the cathodic catalyst displayed promising per‐formance with a maximum power density of 33 mW/cm2 in alkaline media and 47 mW/cm2 in acidic media. The detailed investigation on the composition–structure–performance relationship by X‐ray diffraction, X‐ray photoelectron spectroscopy and Mo-ssbauer spectroscopy suggests that Fe‐N4, together with graphitic‐N and pyridinic‐N are the active ORR components. The promising direct methanol fuel cell performance displayed by the Fe‐N‐C catalyst is related to the intrinsic high catalytic activity, and critically for this application, to the high methanol tolerance.

High-Performance Na-Ion Storage of S-Doped Porous Carbon Derived from Conjugated Microporous Polymers

Na-ion batteries(NIBs)have attracted considerable attention in recent years owing to the high abundance and low cost of Na.It is well known that S doping can improve the electrochemical performance of carbon materials for NIBs.However,the current methods for S doping in carbons normally involve toxic precursors or rigorous conditions.In this work,we report a creative and facile strategy for preparing S-doped porous carbons(SCs)via the pyrolysis of conjugated microporous polymers(CMPs).Briefly,thiophene-based CMPs served as the precursors and doping sources simultaneously.Simple direct carbonization of CMPs produced S-doped carbon materials with highly porous structures.When used as an anode for NIBs,the SCs exhibited a high reversible capacity of 440 mAh g?1 at 50 mA g?1 after 100 cycles,superior rate capability,and excellent cycling stability(297 mAh g?1 after 1000 cycles at 500 mA g?1),outperforming most S-doped carbon materials reported thus far.The excellent performance of the SCs is attributed to the expanded lattice distance after S doping.Furthermore,we employed ex situ X-ray photoelectron spectroscopy to investigate the electrochemical reaction mechanism of the SCs during sodiation-desodiation,which can highlight the role of doped S for Na-ion storage.