Mechanism Of Pore Formation Research Articles

Preparation, characterization and self-foaming mechanism of total-tailings-based foamed glass-ceramics

A kind of foamed glass-ceramics (FGC) that can be used in the construction field was synthesized by self-foaming technology using untreated phosphorus tailings (PT) and coal gangue (CG) as raw materials in this study. The effects of PT addition and sintering temperature on the phase transformation, microstructure, and properties of FGC were explored, also its self-foaming mechanism during the sintering process was revealed. The results showed that FGC with 80 wt.% PT addition had the best comprehensive performances when treated at 1150 °C, whose porosity was 61.6%, bulk density was 1.04 g/cm3, and compressive strength was 10.11 MPa. Based on the theoretical calculation, CaO and K2O included in the tailings acted as sintering aids, promoting the formation of a glassy phase, which increased the pore size and solidified Ba2+ and Ni2+ within FGC. The pore formation mechanism included in-situ pore formation caused by the combustion of C and the gas released by the reduction of Fe2O3 was wrapped by the glassy phase. This self-foaming synthesized FGC from total tailings provided a novel approach to the high-value utilization of tailings and the development of novel environmentally friendly construction materials.

Direct interaction between fd phage pilot protein pIII and the TolQ–TolR proton-dependent motor provides new insights into the import of filamentous phages

Filamentous phages are one of the simplest examples of viruses with a protein capsid that protects a circular single-stranded DNA genome. The infection is very specific, nonlytic, and can strongly affect the physiology or provide new pathogenic factors to its bacterial host. The infection process is proposed to rely on a pore-forming mechanism similar to that of certain nonenveloped eukaryotic viruses. The Ff coliphages (including M13, fd, and f1) have been intensively studied and were used to establish the sequence of events taking place for efficient crossing of the host envelope structure. However, the mechanism involved in the penetration of the cell inner membrane is not well understood. Here, we identify new host players involved in the phage translocation mechanism. Interaction studies by a combination of invivo biochemical methods demonstrate that the adhesion protein pIII located at the tip of the phage binds to TolQ and TolR, two proteins that form a conserved proton-dependent molecular motor in the inner membrane of the host cell. Moreover, invivo cysteine cross-linking studies reveal that the interactions between the pIII and TolQ or TolR occur between their transmembrane helix domains and may be responding to the proton motive force status of the cell. These results allow us to propose a model for the late stage of filamentous phage translocation mediated by multiple interactions with each individual component of the host TolQRA complex.

Petrological Characteristics and Rock Nomenclature of Sedimentary Bauxite Gas Reservoir: A Case Study of Bauxite in Taiyuan Formation of Ordos Basin

With the great breakthrough in natural gas exploration of Paleozoic Taiyuan formation in Longdong exploratory area in the southwestern part of Ordos Basin, it is urgent to solve the petrological nomenclature of sedimentary bauxite, so as to further study the pore formation mechanism, distribution law, and controlling factors of bauxite reservoirs. In this paper, X-ray diffraction, polarizing microscope, scanning electron microscope, and other methods are used to analyze the mineral composition and structure of bauxite rocks in the study area and give appropriate names. The results show that the sedimentary sequence of bauxite in the study area can be divided into five sections: A, B, C, D, and E. The main mineral components are diaspore (C section content can be more than 90%), illite, kaolinite, and chlorite; accessory mineral include anatase and pyrite; trace components include quartz, feldspar, rutile, hematite, and rock salt; and some of the pores are filled with calcite, siderite, and (iron) dolomite. The rock structure is mainly bedding and massive structure, and some of them have geopetal structure. The texture mainly consists of granular texture, grain (powder crystal) texture, gel texture, and algal bonding texture. Considering the special lithology of section A~C and the lack of existing nomenclature method, based on mineral composition and sedimentary fabric, a triangulation classification nomenclature method is established, which adopts structure+texture as secondary name and the main mineral components diaspore-mud-pyrite of the three end-member mineral components as primary name. It can not only highlight the mineral assemblage characteristics of sedimentary sequence of bauxite but also reflect the lithologic characteristics of reservoir development section and the influencing factors of reservoir formation, effectively reflecting the petrological characteristics of bauxite reservoir. Among them, the diaspore rocks with granular, bean-oolitic, and grain texture are the main lithologies forming the natural gas reservoir space of Taiyuan formation in Longdong area. The naming method is feasible and reliable for sedimentary bauxite rocks, which lays a good foundation for the study of natural gas reservoir, pore formation mechanism, and distribution law in Longdong area, southwest of the basin.

Numerical and experimental study on keyhole dynamics and pore formation mechanisms during adjustable-ring-mode laser welding of medium-thick aluminum alloy

Keyhole induced-pore is one of the biggest challenges in laser welding of aluminum alloys. A shaped laser controlling strategy, ring-mode laser, has shown the possibility of reducing porosity in welding due to its potential to enlarge keyhole openings and improve the stability of the keyhole. However, few attempts have been made to reveal the influence of ring-mode laser on keyhole dynamics and pore formation. This paper quantitatively investigated porosity improvement during adjustable-ring-mode laser welding (ARM-LW) of aluminum alloys and analyzed keyhole dynamics and porosity formation mechanisms using a validated model. Experimental results indicate that porosity can be dramatically reduced when compounding a ring laser beam over the Gaussian beam. As the core/ring power ratio adjusts from 10:0 to 5:5, the porosity decreases significantly and remains lower (1.73%∼2.58%) while ensuring a similar melt depth (5∼6 mm). Simulation results demonstrate that two mechanisms work synergistically to suppress porosity: (1) The ring-mode laser contributes to decreasing keyhole collapse and regulating melt pool flow, hence reducing pores created at the Gas-Liquid interface (G/L-pore); (2) The ring-mode laser facilitates reducing the frequency and depth of keyhole into the melt pool, thus minimizing pores created at the Liquid-Solid interface (L/S-pore). This work can guide the porosity suppression during laser welding of aluminum alloys and is of significant theoretical meaning and application value.

Facile preparation of nitrogen-doped microporous carbon from potassium citrate/urea for effective CH4 separation and uptake

N-doped microporous carbons have attracted much attention for micromolecule gas separation and accumulation owning to their superior adsorption potential and surface polarizability. However, to prepare N-doped microporous carbon usually acquire excess corrosive KOH as activator, which limits its application in industry. Here, we propose a non-corrosion method for the manufacture of narrow N-doped microporous carbons using potassium citrate acts as activating agent, and urea acts as both a nitrogen doping agent and coactivator without any solvent. The BET surface area, micropore volume, pore size distribution and N content can be easily adjusted by changing the potassium citrate/urea ratio and activating temperature. The influence of porous structure and N content on CH4 uptake and separation was investigated, and ultra-micropore volume (<1nm) plays a dominate role in CH4 selectivity adsorption. ACK2N1 had the largest CH4 adsorption capacity of 3.00 mmol/g and CH4/N2 selectivity of 7.11 at 273.15 K and 100 KPa due to its largest ultra-micropore volume and N content. The adsorption breakthrough, regeneration experiments and adsorption thermodynamics showed that the prepared well-developed N-doped microporous carbons have very good potential for CH4 separation and enrichment from low coal bed methane. Furthermore, the pore formation mechanism of the well microporous carbon materials is proposed.

Combating fungal phytopathogens with human salivary antimicrobial peptide histatin 5 through a multi-target mechanism.

Blast disease caused by Magnaporthe oryzae is a major contributor to decreased crop yield and rice production globally. The use of chemical fungicides to combat crop pathogens is not only unsafe but also promotes the emergence of pathogenic variants, leading to recurrent host infections. To address plant diseases, antimicrobial peptides have emerged as a promising alternative as they are effective, safe, and biodegradable antifungal agents. This study examines the antifungal activity and mechanism of action of the human salivary peptide histatin 5 (Hst5) on M. oryzae. Hst5 causes morphogenetic defects in the fungus, including non-uniform chitin distribution on the fungal cell wall and septa, deformed hyphal branching, and cell lysis. Importantly, a pore-forming mechanism of Hst5 in M. oryzae was ruled out. Furthermore, the interaction of Hst5 with the M. oryzae genomic DNA suggests that the peptide may also influence gene expression in the blast fungus. In addition to its effects on morphogenetic defects and cell lysis, Hst5 also inhibits conidial germination, appressorium formation, and the appearance of blast lesions on rice leaves. The elucidated multi-target antifungal mechanism of Hst5 in M. oryzae provides an environmentally friendly alternative to combating blast infections in rice by preventing fungal pathogenicity. The promising antifungal characteristics of the AMP peptide may also be explored for other crop pathogens, making it a potential biofungicide for the future.

Geomimetic, Ultrafast, and One-Step Preparation of an N-Doped Reduced TiO2 Porous Layer through an Atmospheric Plasma Spraying Approach for Photocatalytic Tetracycline Removal

A geomimetic, ultrafast, and one-step preparation method for an N-doped reduced TiO2 porous layer using the atmospheric plasma spraying (APS) technique is proposed. The secondary gas provided by the APS (H2) is responsible for reducing TiO2, while an acetamide solution stored in the pores of the substrate acted as a nitrogen source for TiO2 doping. Inspired by the nature of volcanic eruptions on Earth, we used a geomimetic vapor-induced pore-forming (VI-PF) mechanism to produce porous N-doped TiO2 via one-step preparation. We varied the acetamide solution concentration to synthesize different samples (TNX, X indicates the wt % of acetamide solution) to approach photocatalytic tetracycline (TC, 20 ppm/100 mL) degradation under AM1.5G solar simulator irradiation. When the acetamide solution concentration was 5 wt %, the sample (TN5) showed the highest lattice-nitrogen content, which gave it the highest photocatalytic degradation efficiency (rate constant = 1.71 × 10–2 min–1) of TC. Moreover, after 15 rounds of recycling tests, the removal rate and crystalline structure remained stable. In addition to experiments, density functional theory (DFT) calculations are also used to verify the experimental results, and they are also consistent with each other. This work is the first study using the APS technique in a single-step process for nitrogen doping and H2 reduction and is a green, cost-effective, time-saving, and promising method for the mass production of porous TiO2.

Structure formation and properties of a porous aggregate based on man-made waste

The article shows the possibility of obtaining a high-quality porous material with high physical and mechanical properties based on local clay raw materials and man-made waste. The influence of chemical industry waste ― phosphogypsum and alkaline waste of soda production ― on the mechanism of mineral formation and pore formation during the synthesis of lightweight material was studied. It has been established that the used waste accelerates the swelling process during firing, reducing the swelling temperature by 30‒50 o C, while obtaining a durable porous material. Ill. 3. Ref. 20. Tab. 3.

Pore formation driven by particle impact in laser powder-blown directed energy deposition.

Process defects currently limit the use of metal additive manufacturing (AM) components in industries due to shorter fatigue life, potential for catastrophic failure, and lower strength. Conditions under which these defects form, and their mechanisms, are starting to be analyzed to improve reliability and structural integrity of these highly customized parts. We use in situ, high-speed X-ray imaging in conjunction with a high throughput laser, powder-blown directed energy deposition setup to observe powder particle impact behavior within the melt pool. Through fundamental observations of the stochastic, violent powder delivery in powder-blown DED, we uncover a unique pore formation mechanism. We find that a pore can form due to air-cushioning, where vapor from the carrier gas or environment is entrapped between the solid powder particle surface and liquid melt pool surface. A critical time constant is established for the mechanism, and X-ray computed tomography is used to further analyze and categorize the new type of "air-cushioning" pores. It is shown that the air-cushioning mechanism can occur under multiple laser processing conditions, and we show that air-cushioning pores are more likely to be formed when powder particles are larger than 70 m. By quantifying the effect of powder particle impact, we identify new avenues for development of high-quality laser, powder-blown DED products. Furthermore, we deepen knowledge on defect formation in metal additive manufacturing, which is being increasingly utilized in high performance situations such as aerospace, automotive, and biomedical industries.

Bacterial clearance and anti-inflammatory effect of Withaferin A against human pathogen of Staphylococcus aureus in infected zebrafish

The emergence of antibiotic resistance is the most challenging factor for developing a proper drug to treat S. aureus infection. These bacterial pathogens can survive in fresh water and spread to various environments. Plant sources, especially pure compounds, are the material of interest amongst researchers for developing drugs of therapeutic value. Here, we report the bacterial clearance and anti-inflammatory potential of the plant compound Withaferin A, using the zebrafish infection model. The minimum inhibitory concentration of the Withaferin A was calculated as 80 µM against S. aureus. The DAPI/PI staining and scanning electron microscopy analysis showed the pore-forming mechanism of Withaferin A on the bacterial membrane. Along with the antibacterial activity, the results from the tube adherence test reveal the antibiofilm property of Withaferin A. In vivo studies were demonstrated to determine the effect of Withaferin A on survival, inflammatory response and behavioural changes during S. aureus infection. Staining zebrafish larvae with neutral red and Sudan black indicates a substantial decrease in the number of localized macrophages and neutrophils. The gene expression analysis showed the downregulation of inflammatory marker genes. Additionally, we observed the improvement in locomotory behaviour among Withaferin A treatment adult zebrafish. In conclusion, S. aureus can infect zebrafish and induces toxicological effect. In comparison, the results from in vitro and in vivo experiments suggest that Withaferin A can be used for synergistic antibacterial, antibiofilm and anti-inflammatory activity to treat infections due S. aureus.

Silicon carbide ceramic membrane support sintered at 800 °C with low-temperature sintering aid

Silicon carbide ceramic membranes have been widely used in the treatment of various corrosive and high temperature wastewaters. However, SiC is a compound with strong covalent bond, thus the sintering temperature and then the energy consumption during sintering of SiC ceramics is high, which inhibits the scale-up manufacturing of SiC ceramic membranes. Here, a silicon carbide ceramic membrane support was prepared at 800 °C with a low melting-point glaze as the sintering aid. The glaze infiltrated the SiC skeleton during sintering, and gave rise to high fracture strength of the porous ceramics. With the content increase of sintering aid from 10 wt% to 30 wt%, the pore-formation mechanism of the ceramic membrane support transformed from SiC particles packing to SiC aggregations packing, leading to the increase in pore size and decrease in porosity. The permeance and selectivity of the support was investigated via pure-water and oil-in-water emulsion tests. Due to the high hydrophilicity, the pure-water flux increased from 32 L/(m2·h) to 87 L/(m2·h) while the oil rejection decreased from 99.0% to 93.1% with the increase of trans-membrane pressure. This work provides a feasible route for the preparation of SiC porous ceramics with low energy consumption.

Properties of a tardigrade desiccation-tolerance protein aerogel

Lyophilization is promising for tackling degradation during the drying and storage of protein-based drugs. Tardigrade cytosolically abundant heat soluble (CAHS) proteins are necessary and sufficient for desiccation-tolerance in vivo and protein protection in vitro. Hydrated CAHS proteins form coiled-coil-based fine-stranded, cold-setting hydrogels, but the dried protein remains largely uncharacterized. Here, we show that dried CAHS D gels (i.e., aerogels) retain the structural units of their hydrogels, but the details depend on prelyophilization CAHS concentrations. Low concentration samples (<10 g/L) form thin (<0.2 μm) tangled fibrils lacking regular structure on the micron scale. Upon increasing the concentration, the fibers thicken and form slabs comprising the walls of the aerogel pores. These changes in morphology are associated with a loss in disorder and an increase in large β sheets and a decrease in α helices and random coils. This disorder-to-order transition is also seen in hydrated gels as a function of concentration. These results suggest a mechanism for pore formation and indicate that using CAHS proteins as excipients will require attention to initial conditions because the starting concentration impacts the lyophilized product.

Bioactive porous ZrO2-based ceramics with a hierarchical porosity for artificial bone scaffolds

Given the pressing clinical need, the market for artificial bone scaffolds in orthopedics is growing at a rapid rate. In the past, ZrO2-based biomaterials intended for implantation were dense and ‘bio-inert’. Material scientists have now shifted toward the design of deliberately porous and ‘bioactive’ ZrO2-based biomaterials that integrate with human cells and tissues. In this study, we designed and prepared porous and bioactive ZrO2–SiO2 nanocrystalline ceramics. The phase composition, microstructure, pore formation mechanism, and ion release behaviors of the ceramics were explored. The ceramics showed a hierarchical porosity, consisting of connected macropores (∼100 μm or larger) and micropores (∼1 μm). The spherical macropores were formed by a pore-forming agent method, and the irregular micropores were formed because of incomplete densification. The bioactive dopants (Ca and Sr) acted as a destabilizer of tetragonal ZrO2. Ca, Si, and Sr ions continuously released from the surface of the samples, providing good bioactivity for the ceramics. The porous and bioactive ceramics show great potential to be used as artificial bone scaffolds.

Keyhole-induced pore formation mechanism in laser-MIG hybrid welding of aluminum alloy based on experiment and multiphase numerical model

Keyhole-induced pore formation mechanism in laser-MIG hybrid welding of aluminum alloy based on experiment and multiphase numerical model

Porous ceramic membranes from coal fly ash with addition of various pore-forming agents for oil-in-water emulsion separation

Coal fly ash (CFA) is a substitute material for ceramic membrane which can effectively reduce the preparation cost. However, CFA based ceramic membranes usually show insufficient mechanical strength for application. Revealing pore-forming mechanisms of different pore-forming agents in membranes preparation is of great significance to improve mechanical strength without harming permeability. In this work, three different pore-forming agents, carbon powder, dolomite and dextrin, were adopted to prepare CFA membranes. Characters including porosity, pore size distribution and permeability of membranes were comparatively analyzed. Effects of pore-forming agents on membranes were discussed. The membrane with dextrin at 1200 °C sintering showed the best comprehensive properties. Its porosity, flexural strength and Darcian permeability coefficient were 39.46 %, 35.56 MPa and 3.84 × 10−14 m2, respectively. Application in oil-in-water emulsion separation indicated higher than 94 % oil rejection. This research provides experimental bases for improving performances of low-cost CFA membranes, thereby conducive to engineering applications.

Process Parameter Optimization of 2507 Super Duplex Stainless Steel Additively Manufactured by the Laser Powder Bed Fusion Technique

Laser powder bed fusion is an attractive technology for producing high-strength stainless steel alloys. Among the stainless steels, 2507 super duplex stainless steel (2507 SDSS) is known for its excellent combination of corrosion resistance and high strength. Although there are some studies that aimed at optimizing the laser powder bed fusion (LPBF) printing parameters to print highly dense 2507 SDSS parts; However, a full optimization study is not reported yet. This study aims at optimizing the printing parameters for 2507 SDSS, namely: laser power, scan speed, and hatch distance. The response surface methodology was used in generating a detailed design of experiment to investigate the different pore formation types over a wide energy density range (22.22–428.87 J/mm3), examine the effects of each process parameter and their interactions on the resulting porosity, and identify an optimized parameter set for producing highly dense parts. Different process parameters showed different pore formation mechanisms, with lack-of-fusion, metallurgical or gas, and keyhole regimes being the most prevalent pore types identified. The lack-of-fusion pores are observed to decrease significantly with increasing the energy density at low values. However, a gradual increase in the keyhole pores was observed at higher energy densities. An optimal energy density process window from 68.24 to 126.67 J/mm3 is identified for manufacturing highly dense (≥99.6%) 2507 SDSS parts. Furthermore, an optimized printing parameter set at a laser power of 217.4 W, a scan speed of 1735.7 mm/s, and a hatch distance of 51.3 µm was identified, which was able to produce samples with 99.961% relative density. Using the optimized parameter set, the as-built 2507 SDSS sample had a ferrite phase fraction of 89.3% with a yield and ultimate tensile strength of 1115.4 ± 120.7 MPa and 1256.7 ± 181.9 MPa, respectively.

Cryo-EM-based structural insights into supramolecular assemblies of γ-hemolysin from S. aureus reveal the pore formation mechanism

γ-Hemolysin (γ-HL) is a hemolytic and leukotoxic bicomponent β-pore-forming toxin (β-PFT), a potent virulence factor from the Staphylococcus aureus Newman strain. In this study, we performed single-particle cryoelectron microscopy (cryo-EM) of γ-HL in a lipid environment. We observed clustering and square lattice packing of octameric HlgAB pores on the membrane bilayer and an octahedral superassembly of octameric pore complexes that we resolved at resolution of 3.5Å. Our atomic model further demonstrated the key residues involved in hydrophobic zipping between the rim domains of adjacent octameric complexes, providing additional structural stability in PFTs post oligomerization. We also observed extra densities at the octahedral and octameric interfaces, providing insights into the plausible lipid-binding residues involved for HlgA and HlgB components. Furthermore, the hitherto elusive N-terminal region of HlgA was also resolved in our cryo-EM map, and an overall mechanism of pore formation for bicomponent β-PFTs is proposed.

Mechanism and Observation of Pore Formation during Carbonitriding

Abstract Carbonitriding enhances properties of many steels and is therefore an attractive alternative for surface hardening of steel components in the mechanical industry. However, pore formation in the carbon and nitrogen enriched surface layer may occur under certain process conditions. For a given steel and case depth specification, pore formation can be managed by reducing the nitrogen activity of the carbonitriding atmosphere below a defined limit, depending on process temperature and process time. Recent progress in process control allows automatic and independent adjustments of the carbon and nitrogen activities and corresponding potentials of the carbonitriding atmosphere. This study contributes to the practical evaluation of pore formation limits under selected carbonitriding conditions for a range of commonly used engineering steel grades.

Fabrication of Porous Carbon Nanofibers from Polymer Blends Using Template Method for Electrode-Active Materials in Supercapacitor

Porous carbon nanofibers (PCNFs) with excellent physical and chemical properties have been considered candidate materials for electrodes used in supercapacitors. Herein, we report a facile procedure to fabricate PCNFs through electrospinning blended polymers into nanofibers followed by pre-oxidation and carbonization. Polysulfone (PSF), high amylose starch (HAS), and phenolic resin (PR) are used as three different kinds of template pore-forming agents. The effects of pore-forming agents on the structure and properties of PCNFs have been systematically studied. The surface morphology, chemical components, graphitized crystallization, and pore characteristics of PCNFs are analyzed by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and nitrogen adsorption and desorption test, respectively. The pore-forming mechanism of PCNFs is analyzed by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Fabricated PCNF-R have a specific surface area as high as ~994 m2/g, a total pore volume as high as ~0.75 cm3/g, and a good graphitization degree. When PCNF-R are used as active materials to fabricate into electrodes, the PCNF-R electrodes show a high specific capacitance ~350 F/g, a good rate capability ~72.6%, a low internal resistance ~0.55 Ω, and an excellent cycling stability ~100% after 10,000 charging and discharging cycles. The design of low-cost PCNFs is expected to be widely applicable for the development of high-performance electrodes for an energy storage field.

Pore-Forming Proteins: From Pore Assembly to Structure by Quantitative Single-Molecule Imaging.

Pore-forming proteins (PFPs) play a central role in many biological processes related to infection, immunity, cancer, and neurodegeneration. A common feature of PFPs is their ability to form pores that disrupt the membrane permeability barrier and ion homeostasis and generally induce cell death. Some PFPs are part of the genetically encoded machinery of eukaryotic cells that are activated against infection by pathogens or in physiological programs to carry out regulated cell death. PFPs organize into supramolecular transmembrane complexes that perforate membranes through a multistep process involving membrane insertion, protein oligomerization, and finally pore formation. However, the exact mechanism of pore formation varies from PFP to PFP, resulting in different pore structures with different functionalities. Here, we review recent insights into the molecular mechanisms by which PFPs permeabilize membranes and recent methodological advances in their characterization in artificial and cellular membranes. In particular, we focus on single-molecule imaging techniques as powerful tools to unravel the molecular mechanistic details of pore assembly that are often obscured by ensemble measurements, and to determine pore structure and functionality. Uncovering the mechanistic elements of pore formation is critical for understanding the physiological role of PFPs and developing therapeutic approaches.