Particle Surface Research Articles

Chemically Tagging Cargo for Specific Packaging inside and on the Surface of Virus-like Particles.

Virus-like particles (VLPs) have untapped potential for packaging and delivery of macromolecular cargo. To be a broadly useful platform, there needs to be a strategy for attaching macromolecules to the inside or the outside of the VLP with minimal modification of the platform or cargo. Here, we repurpose antiviral compounds that bind to hepatitis B virus (HBV) capsids to create a chemical tag to noncovalently attach cargo to the VLP. Our tag consists of a capsid assembly modulator, HAP13, connected to a linker terminating in maleimide. Our cargo is a green fluorescent protein (GFP) with a single addressable cysteine, a feature that can be engineered in many proteins. The HAP-GFP construct maintained HAP's intrinsic ability to bind HBV capsids and accelerate assembly. We investigated the capacity of HAP-GFP to coassemble with HBV capsid protein and bind to preassembled capsids. HAP-GFP binding was concentration-dependent, sensitive to capsid stability, and dependent on linker length. Long linkers had the greatest activity to bind capsids, while short linkers impeded assembly and damaged intact capsids. In coassembly reactions, >20 HAP-GFP molecules were presented on the outside and inside of the capsid, concentrating the cargo by more than 100-fold compared to bulk solution. We also tested an HAP-GFP with a cleavable linker so that external GFP molecules could be removed, resulting in exclusive internal packaging. These results demonstrate a generalizable strategy for attaching cargo to a VLP, supporting development of HBV as a modular VLP platform.

Effect of carbon fiber structure of Marimo carbon on polymer electrolyte fuel cell performance

Fibrous carbon has attracted attention for use as a carbon support of polymer electrolyte fuel cells (PEFC). In this study, Marimo carbon (MC), a fibrous carbon, was used as the carbon support. The MC has a higher order structure in which many carbon nanofilaments (CNFs) are grown on the surface of diamond particles (dia.). The MC was synthesized by the contact reaction between a Ni supported oxidized diamond (Ni/O-dia.) and CH4 gas, the carbon source of the CNFs. The flow rate of the CH4 gas during the MC synthesis altered the structure of the CNFs. A thick CNFs was observed in the MC with a low CH4 gas flow rate, which was not observed in the MC with a high CH4 gas flow rate. The MC with the thicker CNFs had wider interspaces between the CNFs and higher Pt supporting amounts. Electrochemical measurements of the Pt support MC (Pt/MC) were evaluated by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and current–voltage (I–V) measurements. The lower CH4 gas flow rate of the MC indicated faster charge transfer. The MC structural and charge transfer changed with the flow rate of the CH4 gas altered the electrochemical active surface area (ECSA), the oxygen reduction reaction (ORR) catalytic activity and the I–V performance of the Pt/MC.

Shear thickening in suspensions of particles with dynamic brush layers.

Control of frictional interactions among liquid-suspended particles has led to tunable, strikingly non-Newtonian rheology via the formation of strong flow constraints as particles come into close proximity under shear. Typically, these frictional interactions have been in the form of physical contact, controllable via particle shape and surface roughness. We investigate a different route, where molecular bridging between nearby particle surfaces generates a controllable constraint to relative particle movement. This is achieved with surface-functionalized colloidal particles capable of forming dynamic covalent bonds with telechelic polymers that comprise the suspending fluid. At low shear stress this results in particles coated with a uniform polymer brush layer. Beyond an onset stress σ* the telechelic polymers become capable of bridging and generate shear thickening. Over the size range investigated, we find that the dynamic brush layer leads to dependence of σ* on particle diameter that closely follows a power law with exponent -1.76. In the shear thickening regime, we observe an enhanced dilation in measurements of the first normal stress difference N1 and reduction in the extrapolated volume fraction required for jamming, both consistent with an effective particle friction that increases with decreasing particle diameter. These results are discussed in light of predictions for suspensions of hard spheres and of polymer-grafted particles.

Effects of grain size and seawater salinity on magnesium hydroxide dissolution and secondary calcium carbonate precipitation kinetics: implications for ocean alkalinity enhancement

Abstract. Understanding the impacts that mineral grain size and seawater salinity have on magnesium hydroxide (Mg(OH)2) dissolution and secondary calcium carbonate (CaCO3) precipitation is critical for the success of ocean alkalinity enhancement. We tested Mg(OH)2 dissolution kinetics in seawater using three Mg(OH)2 grain sizes (<63, 63–180 and >180 µm) at three salinities (∼36, ∼28 and ∼20). While Mg(OH)2 dissolution occurred more quickly the smaller the grain size, salinity did not significantly impact measured rates. Our results also demonstrate that grain size can impact secondary CaCO3 precipitation, suggesting that an optimum grain size exists for ocean alkalinity enhancement (OAE) using solid Mg(OH)2. Of the three grain sizes tested, the medium grain size (63–180 µm) was optimal in terms of delaying secondary CaCO3 precipitation. We hypothesise that in the lowest-grain-size experiments, the higher surface area provided numerous CaCO3 precipitation nuclei, while the slower dissolution of bigger grain sizes maintained a higher alkalinity and pH at the surface of particles, increasing CaCO3 precipitation rates and making them observable much more quickly than for the intermediate grain size. Salinity also played a role in CaCO3 precipitation, where the decrease in magnesium (Mg) allowed secondary precipitation to occur more quickly, similar in effect size to another known inhibitor, i.e. dissolved organic carbon (DOC). In summary, our results suggest that OAE efficiency as influenced by CaCO3 precipitation depends not only on seawater composition but also on the physical properties of the alkaline feedstock used.

From Cauliflowers to Microspheres: Particle Growth Mechanism in Self-Stabilized Precipitation Polymerization.

Self-stabilized precipitation (2SP) polymerization enables the facile synthesis of uniform polymer spheres with sizes ranging from 100 nm to 3 μm, without the need for stabilizers or cross-linkers, even at high monomer concentrations of up to 30%. While previous studies have extensively explored the influence of reaction conditions on the size and uniformity of microsphere products, their impact on particle morphology has received less attention. In this work, we demonstrate that particle growth in 2SP polymerization primarily occurs via the adsorption of polymers from the solution onto the particle surface, leading to an increase in particle circularity and a smoother surface. The surface roughness of the particles is controlled by the aggregation of primary particles and the subsequent polymer adsorption process during the growth stage. Smooth microspheres are obtained under conditions of moderate monomer concentration, high initiator concentration, and elevated temperature. Our findings highlight the significance of the particle growth process in determining particle morphology in addition to the well-established role of polymer-solvent interactions during precipitation polymerization.

Preparation and mechanism research on hydrophobic coupling modification of HTV silicone rubber

Neat high-temperature vulcanized silicone rubber (HTV SR) showed bad hydrophobicity due to the existence of a large number of inorganic reinforcing fillers on its surface, which affected its security application in outdoor insulation systems. In this work, hydrophobic silane chains were grafted onto the surface of inorganic particles on the skin layer of HTV SR by a one-step coupling modification to improve its hydrophobicity. The effects of coupling agent types and coupling reaction conditions on the hydrophobicity of HTV SR were investigated. It was determined that the perfluorooctane trichlorosilicon with a large number of low surface energy fluorine atoms was the preferred coupling agent. The contact angle of HTV SR was increased by 15.70% when the optimal coupling reaction conditions were determined to be a reaction temperature of 60°C, a reaction time of 4 h, and an amount of coupling agent of 0.5%. The study found that both etching reaction and grafting reaction occurred during the whole coupling modification process, which led to the disappearance or decrease of a lot of holes on the HTV SR surface. After the fluorination coupling reaction, the surface of HTV SR became smooth and dense that led to the decrease of water absorption. The result of Fourier-transform infrared spectroscopy analysis showed the formation of C-F bond in HTV SR after fluorination modification, and the energetic dispersive spectroscopy analysis showed that the fluorine content on the surface of the fluorinated HTV SR increased significantly. Moreover, the stability analysis showed that the fluorinated HTV SR still had a good thermal stability and mechanical property stability.

Unveiling the Hidden Networks: AFM Insights into Pre‐Vulcanized Hevea Latex and Its Profound Impact on Latex Film Mechanical Properties

AbstractNatural rubber (NR) films with different natural networks—concentrated NR (CNR), deproteinized NR (DPNR), and small rubber particles (SRP)—are investigated to explore the relationship between network structure and film properties using atomic force microscopy (AFM) in PeakForce Quantitative Nanomechanics (QNM) mode. Nitrogen content, gel content, and particle size distribution analyses reveal distinct network topologies in each latex type. Mechanical testing shows variations in tensile strength and crosslink density. AFM analysis provides insights into the crosslink network structures within the pre‐vulcanized latex film. It is found that DPNR and CNR films have a uniform distribution of crosslink networks, with DPNR exhibiting higher Young's modulus values. In contrast, SRP shows varying Young's modulus values, suggesting poor coalescence arising from a harder particle surface and a softer rubber core in an inhomogeneous network structure intrinsic to the non‐rubber components (NRCs) make‐up of SRP latex. This study highlights the pivotal role of natural network structures formed by NRCs in determining the ultimate properties of latex films, which has significant implications for the rubber industry, particularly in the production of latex‐dipped products, medical devices, and bioengineering applications.

New experimental method for the simultaneous determination of concentration and size profiles of condensed combustion products around a burning aluminum droplet

When an aluminum particle burns in the diffusive regime, a cloud of nanometric particles of its primary oxide, alumina, is formed around the droplet. Characterizing this oxide smoke surrounding a burning aluminum droplet is essential. The original contribution of this paper is to introduce an experimental approach that allows for simultaneous size and concentration measurement of the particles composing the oxide smoke. This paper employs an electrodynamic levitator to facilitate the self-sustained combustion of an isolated aluminum particle, with a radius of 35μm, in atmospheric air. This levitation apparatus is paired with an optical setup that allows for a multi-spectral light extinction method. This technique is specifically designed to measure the size and concentration of alumina particles below the micrometric scale, which is scarcely documented in existing literature. Consequently, spatially resolved concentration and size profiles of the nanometric alumina particles are measured and compared to simulated data from the literature. The radii of alumina particles in the cloud are found to evolve closely around 80 nm. Volume fractions are evaluated from 2.8⋅10−4 near the particle surface to 3⋅10−5 further in the cloud. Therefore, significant concentrations of alumina particles are revealed during the short (15 to 20 ms) combustion process at distances of the order of magnitude of a few initial particle diameters. Such characterization could then lead to a better assessment of the interaction distance among aluminum particles as they burn collectively.Novelty and significance statementThis article introduces the first experimentally determined profiles of alumina concentration and size distribution surrounding a single burning aluminum droplet. The uniqueness of our experimental setup lies in its ability to study of the most fundamental case of the autonomous combustion of a single levitating particle, without any convective effects. A new non-intrusive method specifically designed provides unprecedented results in the field of metallic particle combustion. Data provided in the paper are crucial as they serve as the first reference case for future simulation and experiments. The results introduced in this paper highlight the inability of current simulation methods to accurately account for nucleation and condensation processes, and emphasize the need for a non-invasive characterization method.

Infrared emissivity of icy surfaces

Context. Most analyses of the infrared emission of Saturn’s rings and icy satellites have considered pure water ice as the constituent of regolith and particle surfaces. Visual and near-infrared observations have shown, however, that darkening and reddening contaminants are present at a fraction level of a few percent. In the spectral domain 10–2000 cm−1, water ice becomes transparent in a few windows, which in particular causes the roll-off of emissivity of icy surfaces that is observed below 50 cm−1. Their emissivity there may be affected by these contaminants. Aims. We present a quantitative global sensitivity analysis of a hybrid Mie-Hapke model to evaluate the influence of regolith properties and contaminant fraction on the infrared emissivity of icy rings or moons over this spectral range. Methods. A hybrid Mie–Hapke model of the hemispherical emissivity ε*h(Wn) was made, including various diffraction correction and mixing types with tholins or amorphous carbon grains, or grain size distributions and some anisotropy in emission. A Sobol global sensitivity analysis provided quantitative levels of importance for these factors versus wave number wn. Results. Given the a priori uncertainties, the most important factor acting on ε*h(Wn) remains the size distribution of regolith grains and the average anisotropy factor ξ. For wn> 50 cm−1, ξ, the power-law index p and the minimum amin of the size distribution are most influential. In windows of water-ice transparency (10–50, 300–600, and 900–1300 cm−1), the emissivity is also sensitive, but to a lesser extent, to the maximum grain size amax and the fraction f of contaminants, if mixed at the molecular level. Conclusions. This model provides a self-consistent tool for interpreting multi-modal observations of the thermal emission from icy surfaces. It also offers interesting insights into recent mid-infrared observations of Saturn’s rings and Jupiter’s moon Ganymede by the JWST-MIRI instrument.

Dual Modification Strategy for Enhanced Cycling and Rate Performance of Ni-Rich Cathode Materials in Lithium-Ion Batteries.

A great challenge in the commercialization process of layered Ni-rich cathode material LiNixCoyMn1-x-yO2 (NCM, x ≥ 80%) for lithium-ion batteries is the surface instability, which is exacerbated by the increase in nickel content. The high surface alkalinity and unavoidable cathode/electrolyte interface side reactions result in significant decrease for the capacity of NCM material. Surface coating and doping are common and effective ways to improve the electrochemical performance of Ni-rich cathode material. In this study, an in situ reaction is induced on the surface of secondary particles of NCM material to construct a stable lithium sulfate coating, while achieving sulfur doping in the near surface region. The synergistic modification of lithium sulfate coating and lattice sulfur doping significantly reduced the content of harmful residual lithium compounds (RLCs) on the surface of NCM material, suppressed the side reactions between the cathode material surface and electrolyte and the degradation of surface structure of the NCM material, effectively improved the rate capability and cycling stability of the NCM material.

Porous Silica Nanomaterials as Carriers of Biologically Active Natural Polyphenols: Effect of Structure and Surface Modification

For centuries, humans have relied on natural products to prevent and treat numerous health issues. However, biologically active compounds from natural sources, such as polyphenols, face considerable challenges, due to their low solubility, rapid metabolism, and instability, which hinder their effectiveness. Advances in the nanotechnologies have provided solutions to overcoming these problems through the use of porous silica materials as polyphenol carriers. These materials possess unique properties, such as a high specific surface area, adjustable particle and pore sizes, and a surface that can be easily and selectively modified, which favor their application in delivery systems of polyphenols. In this review, we summarize and discuss findings on how the pore and particle size, structure, and surface modification of silica materials influence the preparation of efficient delivery systems for biologically active polyphenols from natural origins. The available data demonstrate how parameters such as adsorption capacity, release and antioxidant properties, bioavailability, solubility, stability, etc., of the studied delivery systems could be affected by the structural and chemical characteristics of the porous silica carriers. Results in the literature confirm that by regulating the structure and selecting the appropriate surface modifications, the health benefits of the loaded bioactive molecules can be significantly improved.

Synthesis and alloying of zinc sulfide in a homogeneous system based on dodecane, its identification and optical properties

Zinc sulfide doped with Mn2+ ions was synthesized in a homogeneous dodecane medium by the method of emerging reagents. By methods of chemical and X-ray phase analysis, IR spectroscopy, electron microprobe microscopy, identification of products was carried out, photographs of the surface of powder particles (SEM) were recorded. Based on the totality of the results, a conclusion is made about the formation of nanoscale objects having a polytype structure with a predominance of distorted cubic crystals forming agglomerates up to 10 microns in size in ZnS powder and up to 100 microns in ZnS–Mn powder. The formation of nanoscale ZnS particles is confirmed by spectral data. The effect of manganese ions on the photoluminescence (FL) of the powder is manifested by a change in the type of the descending branch of the ZnS–Mn FL band, it is associated with recombination processes at the levels of defects formed by Mn2+ ions in the ZnS structure at their low concentration.

Dust particle surface potential in an argon-helium plasma using the (r,q)-distribution function

Abstract In this paper, the dust particle surface potential for argon-helium plasma is evaluated analytically and numerically in the context of negatively charged dust particles by employing a power-law r , q -distribution function. Recent studies have reported the argon-helium plasma and conducted a brief theoretical and experimental survey. To deepen our understanding further, this study aims to analyze the argon-helium plasma comprehensively using the same pattern but with the r , q -distribution function. For this purpose, the current balance equations are derived for electron, helium and argon ions, when these charge species attain the quasineutrality condition. We numerically examined the currents of plasma species for a broad range of effective distribution function parameters r and q . It is revealed that the surface potential of dust particles is significantly affected by the parameters r and q , helium ion-to-electron temperature ratio, argon ion-to-electron temperature ratio, and helium ion to argon ion number density ratio. By incorporating the multi-ion (argon-helium) species, the significance of low-temperature non-Maxwellian dusty (complex) plasma is briefly examined.

Comparison of Escherichia coli Responses to Different Silver Nanoparticles with Different Particle Sizes and Surface Coatings

AbstractAgNPs are widely used for their excellent antimicrobial properties, whereas the cytotoxicity they possess makes them an unignorable environmental problem. Considering the impact of particle size and surface coating on the antibacterial properties, four types of AgNPs are selected: citrate‐coated 20 nm (C20), polyvinylpyrrolidone‐coated 20 nm (P20), citrate‐coated 100 nm (C100), and polyvinylpyrrolidone‐coated 100 nm (P100) AgNPs. All four AgNPs significantly affect the ribosome pathway, with stronger binding of large and small subunits. 20 nm and 100 nm AgNPs both affected the biosynthesis and metabolism of several amino acids (including arginine, glycine, serine, threonine, glyoxylic acid, and dicarboxylic acid). P20 and C100 exposure affected bacterial chemotaxis and flagellar motility. This study preliminarily explained the response mechanism of E. coli to AgNPs with different properties, which provided a theoretical basis for predicting the response mechanism of E. coli to metal nanoparticles with similar properties.

Effects of Relative Humidity and Phase on the Molecular Detection of Nascent Sea Spray Aerosol Using Extractive Electrospray Ionization.

Online mass spectrometry techniques, such as extractive electrospray ionization mass spectrometry (EESI-MS), present an attractive alternative for analyzing aerosol molecular composition due to reduced aerosol sample collection and handling times and improved time resolution. Recent studies show a dependence of EESI-MS sensitivity on particle size and mixing state. This study measured authentic sea spray aerosol (SSA) components generated during a phytoplankton bloom, specifically glycerol, palmitic acid, and potassium ions. We demonstrate temporal variability and trends dependent on specific biological processes occurring in seawater. We found that the EESI-MS sensitivity, after adjusting for pressure variations at the inlet and normalizing to the reagent ion, critically depends on the sample's relative humidity. Relevant SSA species exhibited heightened sensitivity at an elevated relative humidity near the deliquescence relative humidity of sea salt and poorer sensitivity with sparse detection below the efflorescence relative humidity. Modeling the reagent ion's diffusive depth demonstrates that the sample aerosol particle viscosity governs the relative humidity dependence because it modulates the particle's coagulation efficiency and distance the reagent ion diffuses and reacts with components in the particle bulk. The effects of particle size and mixing state are discussed, revealing improved sensitivity of phase-separated components present along the particle surface. This work highlights the importance of the particle phase state in detecting and quantifying molecular components within authentic and complex aerosol particles and the utility of EESI-MS for measuring SSA composition.

Icosahedral Quasicrystalline Phase on the Surface of Spherical Particles in Al-Cu-Fe Alloy

Icosahedral Quasicrystalline Phase on the Surface of Spherical Particles in Al-Cu-Fe Alloy

A symmetric chiral aromatic polyamide modified silica material combining rigid-flexible and application in liquid chromatography

The development of new separation materials is an effective way to improve the separation efficiency of chiral and achiral analytes. Here, a C3-symmetric chiral tricarboxylic acid compound was prepared and successfully immobilized onto the surface of porous silica particles by a one-pot synthesis strategy. The resulting material (TPHs-SiO2) was composed of symmetric chiral aromatic polyamide with a combination of rigid-flexibility, which gave it both chiral and hydrophilic interaction/ion exchange (HILIC/IEC) characteristics. TPHs-SiO2 as a new stationary phase for liquid chromatography can separate 1-phenyl-ethanol, 1-phenyl-propanol, 1-phenyl-1,2-ethylene glycol, 4-chloro-a-methylbenzyl alcohol, ofloxacin and mandelic acid in normal phase chromatography (NPLC) with resolutions of 2.69, 5.89, 4.49, 1.04, 1.73 and 5.47, respectively, thus indicating that TPHs-SiO2 has chiral resolution performance. TPHs-SiO2 can also achieve the separation of achiral compounds, such as nucleosides, nucleotides, and aniline compounds in HILIC/IEC mode. Therefore, the prepared stationary phase can be used as an ideal multifunctional separation material with chiral separation capability and mixed-mode separation capability (HILIC/IEC), realizing the separation of chiral compounds and different types of compounds. This work provides a new idea and method for developing multifunctional separation materials with multi-selectivity and high efficiency, that has important theoretical and application value.

Predicting the Electrophoretic Mobility of Charged Particles in an Aqueous Medium.

Electrophoresis of charged particles has important applications in biochemical separation processes. The mobility of these particles depends on the surrounding electric double layer (EDL), which is impacted by solvent restructuring because of hydration interactions. Nevertheless, most theoretical estimates ignore such interactions during computation of the electrophoretic mobility. Here, we employ a complementary blend of mean-field analysis and molecular dynamics simulations performed for a peptide-G-quadruplex complex to assess how hydration interactions alter the mobility of a charged particle in an aqueous medium. These interactions are seen to stabilize the EDL, resulting in more significant localized counterion concentrations while strengthening the ensuing electrokinetic flow. The ordering of ions near the particle surface is obtained only upon including hydration interaction, revealing that the hydration water molecules act as a glue for forming a stable EDL, a key finding of this work. Conversely, the observed microstructure of ions near the charged surface as obtained from our theory establishes a bridge link between the micro and continuum model. The presence of larger counter ions enhances the drag on the particle, thus restricting its mobility. The mobility also becomes dependent on size, which may be useful for isolating a wide array of biomolecules. The impact of hydration interactions intensifies with increases in particle size, surface charge density, and bulk ion concentration.

MAF process for aluminum 6060: An analytical temperature modelling and chemo-mechanical analysis

The magnetic abrasive finishing process is a sophisticated micro-finishing process that enhances the surface quality of superalloys, ceramics, and composites. Surface temperature plays a pivotal role in facilitating chemo-mechanical reactions between the processed surface and abrasive particles. In triggering the chemo-mechanical response of the micro-finished surface of Aluminum 6060 (Al-6060), an analytical thermal model derived using Jaeger moving heat formulation to find the flash temperature (FT) and flash time duration (FTD) at the micro-finishing interface of the processed workpiece and the abrasive particles of the magnetic abrasive brush. Furthermore, the present work performed an RSM-based Box Behnken design experiment to analyse and explain the crucial role of machining gap, abrasive weight, Voltage, and rotational speed on surface temperature, machining surface, and hardness. ANOVA highlighted key factors in machining responses. Surface roughness and temperature were notably influenced by voltage (58.42 % and 57.62 %, respectively), while surface hardness primarily depended on abrasive weight (60.65 %). Using the developed model, extreme FT of 880 °C and 810 °C were calculated under specific conditions, along with corresponding FTD required for quasi-steady-state conditions. FT and FTD were identified as sufficient for initiating chemo-mechanical action in the MAF micro-finishing process, depending on contact pressure, the number of abrasive particles, and sliding velocity, which in turn are influenced by magnetic intensity, abrasive ratio, and rotational speed. Furthermore, a detailed examination of the finished surface was carried out using the SEM, EDS and XRD of Al-6060 which shows that the SiC does participate on the finishing surface. Chemical substrates such as Kaolinite (Al2O9Si2), Iron silicide (FeSi), and Cristobalite (O2Si) had formed on the finished surface of Al-6060 due to the chemo-mechanical action between the SiC and workpiece material.

Effect of ferrotitanium slag particle size on properties of Al2O3–SiC–C castables

Ferrotitanium slag can be used to replace bauxite to fabricate refractories owing to its high refractoriness (>1790 °C) and Al2O3 content (≥70 wt%). However, impurities in the ferrotitanium slag is harmful to the materials. In this paper, the mechanical properties and molten slag resistance of Al2O3–SiC–C castables were improved by replacing part of bauxite with large size ferrotitanium slag (8-5 mm). The large size ferrotitanium slag contained a small amount of impurities, which reacted with SiO2 at high temperature to form CaO–Al2O3–SiO2–TiO2 liquid layer on the surface of particles. Under the action of the liquid phase, the ferrotitanium slag particles and the matrix were combined more closely. With the decrease of the particle size of ferrotitanium slag, the slag resistance of the castables began to decrease. This was because the specific surface area of the particles with smaller particle size was relatively larger, large contact area with molten slag resulted in worse slag resistance. Meanwhile, decreasing ferrotitanium slag particle size brought the increase of apparent porosity of Al2O3–SiC–C castables, resulting in weak mechanical properties.