Decreasing Pore Size Research Articles

The Impact of Acid Strength and Mineral Composition on Spontaneous Imbibition with Reactive Fluids

Capillary rise experiments are conducted in a set of calcareous and siliceous rocks with varying mineralogy and petrophysical properties to understand the coupled impact of reactivity and spontaneous imbibition. A capillary rise experiment is performed in each sample: first with deionized water, then with a dilute acidic solution, and finally again with deionized water, and the capillary rise profile for each is recorded. Pre- and post-acid petrophysical properties such as porosity, permeability, pore size distribution, and contact angle are measured for each sample. The mineral makeup of the rocks significantly influences how the acidic fluids penetrate the samples. The primary reactions are the dissolution of Ca- and Mg-rich minerals which alter the pore network. The higher acid strength results in higher capillary rise in calcareous rocks and results in an increase in the average pore size. The same pH acid results in lower capillary rise in the siliceous rocks, and a general decrease in the average pore size is observed. Changes in contact angle indicate increased water affinity in carbonate and reduced affinity in sandstone. The link between capillary interactions and fluid reactivity is often overlooked in fluid flow studies, and this research sheds light on the importance of reactivity during spontaneous imbibition, offering insights into dissolution and precipitation processes during capillary flow.

Developing Innovative Nano-Engineered Lightweight Foamed Concrete Incorporating Iron Oxide (II, III) with Enhanced Mechanical and Transport Properties

Recently, scientists have focused substantial attention on the incorporation of nanoscale components in cement-based materials. Iron oxide (II, III) nanoparticles (IONPs) have garnered significant attention in nanoparticle research. This paper portrays preliminary discoveries of an investigation assessing the characteristics of foamed concrete (FC) with the presence of IONPs. A comprehensive assessment of characteristics was conducted, including its workability, axial compressive strength, bending strength, tensile strength, apparent porosity and water absorption capacity. Furthermore, scanning electron microscope examination was performed and evaluated. The results indicate a significant enhancement in the FC strength characteristics, with 28-day compressive, tensile, and bending strengths improving by up to 70, 76 and 52 %, respectively, with the inclusion of 3 % IONPs. Nonetheless, adding IONPs beyond 3 % did not yield significant improvements in mechanical properties. With a rise in IONPs from 1 to 5 %, the FC exhibited significant improvements in apparent porosity and water absorption. The decreasing pore size in FC containing IONPs was found to be the cause of the anomalies. A significant alteration in the arrangement of pore dimensions was noted in FC mixtures when the amounts of IONPs were modified. Results from this investigation emphasise the prospective benefits associated with integrating IONPs into FC, that could boost its entire characteristics.

Development and evaluation of antibacterial nanofiber membranes via coaxial electrospinning for enhanced air filtration performance

As industrialization intensifies and the population soars, the challenge of air pollution escalates into a pressing concern. Electrospun nanofiber membranes, owing to their distinctive attributes including high specific surface area, porosity, and uniform pore size distribution, have emerged as promising candidates for air filtration. In this study, we successfully prepared ZnO@polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) antibacterial nanofiber membranes through a combined solvothermal and coaxial electrospinning approach. The structure and performance of these nanofiber membranes were systematically modulated by adjusting the shell feeding rate and zinc acetate dihydrate (Zn(Ac)2·2H2O) concentration. Specifically, an increase in the shell feeding rate led to a decrease in fiber diameter, accompanied by the proliferation of nano-beads, thereby contributing to a reduction in membrane pore size. Consequently, a heightened shell feeding rate correlated positively with both filtration efficiency and pressure drop. Furthermore, the incompletely reacted Zn(Ac)2·2H2O enhanced the conductivity of the spinning solution, facilitating a decrease in pore size and enhancing air filtration performance. In summary, when the shell feeding rate was 0.60 mL h−1 and Zn(Ac)2·2H2O concentration was 1.5 wt%, the obtained ZnO@PVDF-HFP nanofiber membrane exhibited superior air filtration performance, with high filtration efficiency of 99.91 %, low pressure drop of 80.70 Pa and noteworthy quality factor of 0.08781 Pa-1. Notably, these membranes sustained their high filtration efficiency and low pressure drop even after 40 min of continuous testing, underscoring their exceptional stability. In addition, the obtained nanofiber membrane exhibited robust antibacterial activity against both Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), demonstrating their multifaceted potential. Our work not only simplifies the fabrication process of electrospun nanofiber membranes with superior air filtration and antibacterial properties but also highlights their potential as innovative alternatives to conventional air filter materials, poised for diverse practical applications.

Body Scrub Salt Formulation from Cinnamomum burmannii (C. Ness & T. Ness) Blume Extract as an Antibacterial Against Staphylococcus aereus

Skincare is currently a major focus in the beauty industry with skin exfoliation being an important step. One product used to exfoliate the skin is a body scrub, which contains ingredients such as himalayan salt and cinnamon bark extract. Himalayan salt helps remove dead skin cells and moisturizes the skin, while cinnamon extract has antimicrobial properties that can protect the skin from bacteria. This study aims to formulate and test the effectiveness of body scrub with skin analyzer and antibacterial activity against Staphylococcus aureus. This research uses an experimental method with several stages, namely plant material collection, plant identification, powder making, extract making, preparation making, evaluation and stability, effectiveness test with skin analyzer and antibacterial activity against Staphylococcus aureus. The 10% body scrub has better effectiveness than 0%; 2.5% and 5% which obtained a percent increase in skin moisture (71.62%), a decrease in the number of blemishes on the skin (70.73%) and a decrease in pore size on the skin (76.38%) for 4 weeks of treatment. In testing antibacterial activity, the 10% concentration was also considered the optimal concentration because it had the greatest inhibition of 14.20 ± 0.59 mm. The results concluded that Himalayan salt and cinnamon bark extract can be formulated into a body scrub dosage form that meets the stability requirements and has the effectiveness in moisturizing, smoothing, and brightening the skin. The formula that has the most effective antibacterial activity is a body scrub containing extracts with a concentration of 10% against Staphylococcus aureus bacteria.

Equation of state for nanopores and shale: Pore size–dependent acentric factor

Nanopores pose a challenge to phase-behavior modeling when using the equation of state (EOS), and common methods do not capture their vapor pressure or become difficult to implement because they require additional tuning parameters. This study focuses on improving the vapor-pressure prediction of EOS in nanopores by proposing a pore size–dependent acentric factor (ACF). It determines the ACF from experimental data and implements it in EOS along with critical pressure and temperature. The proposed approach is then applied to the vapor-pressure measurements of nitrogen, argon, oxygen, methane, and ethane in pores ranging from 3.5 nm to 8.1 nm. The results show that the ACF in nanopores increases as the pore size decreases, and the degree of size dependency varies across different pure components. The results also demonstrate that the proposed approach enables EOS predictions to match the measurements with good accuracy. This study quantifies the effects of pore size on the ACF for the first time and presents simple correlations for estimating the ACF when the pore radius is smaller than 10 nm. The proposed approach simplifies the application of EOS in nanopores and unconventional hydrocarbon reservoirs.

Modulating interfacial Zn2+ deposition mode towards stable Zn anode via bimetallic co-doped coating

Artificial coatings represent the promising means to address the interfacial issues of Zn anode, but it poses a significant challenge to their stability due to the fatigue and resulting cracking of coatings during repeated cycling. Here, a functional coating with the synergistic effect of bimetallic co-doping was developed, which changes the Zn2+ deposition mode to interlayer deposition in coating. The simultaneous doping of Cu2+ and In3+ reduces the pyrrolic N content and enhances the adsorption of Zn2+ in the active sites. Bimetallic co-doping results in an increase in specific surface area and a decrease in pore size, thus providing more active sites. As well as enhanced electrical conductivity, electrons can enter between the coatings, thus promoting redox reactions between the layers. Therefore, it endows surface coating with low polarization and stress buffering simultaneously, which avoids cracking and stripping of coatings during cycling. As a result, the cycle life of CuInZIF-8@Zn||CuInZIF-8@Zn symmetric cell exhibits more than 1200 h at 5 mA cm−2 and 5 mAh cm−2. The CuInZIF-8@Zn anode can match multiple types of cathodes and achieve excellent cycling stability; For instance, it can cycle stably for 3000 cycles when paired with vanadium-based cathode. This work provides a new perspective of artificial coatings towards highly stable Zn anode.

Adaptable Plasmonic Membrane Sensors for Fast and Reliable Detection of Trace Low-Micrometer Microplastics in Lake Water.

In freshwater environments, low-micrometer microplastics (LMMPs) have captured significant attention due to their prevalence and toxicity. Yet, rapid detection of LMMPs (1-10 μm) at the single-particle level within complex freshwater matrices remains a hurdle. We developed an adaptable plasmonic membrane sensor for fast detection of individual LMMPs in eutrophic lake waters. The plasmonic membrane sensor functions both as a membrane filter and as a sensor for LMMP collection and analysis. Among the four types of membrane sensors, polycarbonate track-etch (PCTE) membrane sensors exhibit superior imaging quality for LMMPs due to their flat and homogeneous surfaces. Besides the significantly improved imaging contrast and reduced background interferences, the Raman intensity of LMMPs is enhanced by 48% ± 25% on PCTE membrane sensors compared to unmodified membranes. The increased Raman intensities of a chemical probe with an increasing gold layer thickness and a decreasing membrane pore size suggest a surface-enhanced Raman scattering effect from the membrane sensors. The membrane sensors achieve a detection limit of 1 μg/L and an ultrafast scanning time of 0.01 s for individual LMMPs across natural eutrophic lake water. The developed membrane sensors offer an adaptable tool for the swift and reliable detection of individual LMMPs in complex environmental matrices.

3D-printed gradient conductivity and porosity structure for enhanced absorption-dominant electromagnetic interference shielding

The application of 3D printing for the development of electromagnetic interference (EMI) shielding materials is currently constrained by a limited range of material options and design schemes. In this work, we developed conductivity-modulated polylactic acid (PLA)-MXene composite filaments for fused deposition modeling (FDM) 3D printing, demonstrating excellent printability and durability. Utilizing these filaments, we propose a design scheme focused on absorption-dominant EMI shielding materials. Our design features non-conductive PLA with larger pores at the incident surface, transitioning to layers with increasing conductivity and decreasing pore sizes. This gradient structure minimizes reflection by providing impedance matching and enhances absorption by extending the propagation path of EM waves through multiple reflections and scattering within the pores. Additionally, interfacial polarization effects between air, PLA, and MXene nanoflakes strengthen the absorption mechanisms. Both simulation and experimental results confirm that the combined gradient conductivity and pore size structures significantly improve EMI shielding effectiveness (EMI SE) and absorptivity, achieving an EMI SE of 65 dB and an absorptivity of 0.76 in the X-band. Our findings underscore its potential to create adaptable, high-performance EMI shields suitable for complex geometries and reducing secondary interference.

Phase behavior analysis of methane confined in nanopores using molecular simulation

Interest in the phase behavior of hydrocarbons in shale reservoirs has grown in recent years. Petroleum fluid phase behavior has been observed to differ significantly between conventional reservoirs and shale reservoirs. Within shale reservoirs, notable surface-fluid interactions can lead to non-uniform molecule distribution and an alteration in fluid phase behavior, primarily caused by the existence of nano-scale porous materials. In this work, we study the phase behavior of methane in single cylindrical pore models. We apply the gauge Gibbs ensemble Monte Carlo (gauge-GEMC) simulation technique to investigate the phase behavior of methane in 4–10 nm single nanopores and calculate the saturation pressures at various temperatures using the grand canonical Monte Carlo (GCMC) simulation technique. A shift in the phase diagram has been found for methane in nanopores. As pore size decreases, the shift becomes more significant.

Nanoconfinement of MgO in nitrogen pre-doped biochar for enhanced phosphate adsorption: Performance and mechanism

Advanced metal-doped biochar with superior phosphate (P) adsorption capacity plays a crucial role in combating eutrophication, depending on the rational design of the biochar structure for uniform and nanoscale dispersion of metal oxides. Herein, the nanoconfinement of magnesium oxide (MgO) was successfully attained in nitrogen pre-doped biochar (Mg/N-BC). The well-dispersed MgO was confined within nanoscale structure of Mg/N-BC, delivering P adsorption capacity of 108.41 mg g−1 and adsorption rate of 18.01 mg g-1h−1. More importantly, its adsorption performance at equilibrium 0.5 mg P/L was 17.70 times higher. Results suggested the decrease in pore size was positively correlated with the increase of N, confirming the role of N pre-doping in structure shaping and MgO confinement. The enhanced P adsorption was attributed to the well-dispersed MgO nanoparticles within the biochar. This study introduced a facile synthesis approach for biochar-incorporated nanoscale MgO, offering a new strategy for enhanced P removal.

Microscale insights into deep bed membrane filtration: Influence of internal surface roughness

Deep bed filtration is widely applied in bioprocessing, virus filtration, and water purification to remove small impurities, such as particles or virus fragments. However, more needs to be understood about the parameters that influence particle capture and deposition. Detailed simulations and microfluidic filtration experiments with straight pores have been widely investigated, yet realistic membrane porosity features such as pore gradients and roughness have not been addressed in detail. The internal membrane morphology is assumed to have a strong effect on filtration performance. Therefore, this study introduces a new microfluidic membrane mimicking device (MMD) and methodology that analyzes spatio-temporal particle collections in a deep bed filtration MMD with gradually decreasing pore size toward the retentate side. The design allows us to systematically tailor an internal filter surface roughness to investigate its influence on differently sized soft particles and the consequences for filtration performance, in particular, particle capture. Optical investigation and quantitative evaluation show enhanced particle–pillar interactions for increased roughness. This results in a reduced penetration depth and reduced particle breakthrough. The modes of capture or filtration phenomena, such as pore blocking, bridging, or dendrite formation, differ significantly between smooth and rough membrane filter structures. In the case of rough inner filter surfaces, those phenomena lead to a less distinct decrease in volumetric flow, allowing a longer filtration process. The microfluidic study offers a detailed investigation of how microscale phenomena influence the filtration process. The results provide a fundamental understanding of microscale filtration effects based on roughness and, hence, motivate a tailoring of the internal membrane filter surface according to the filtration problem at hand.

Nanoconfinement effect on the miscible behaviors of CO2/shale oil/surfactant systems in nanopores: Implications for CO2 sequestration and enhanced oil recovery

Currently, CO2 flooding is the most promising carbon capture, utilization, and storage (CCUS) technology in the energy industry. Understanding the nanoconfinement effect on the CO2-oil miscible process is crucial for accurately determining the minimum miscibility pressure (MMP) of CO2/oil in shale reservoirs. In this study, we conducted molecular dynamics (MD) simulations to investigate the effects of pore size, surfactants, and pore type on the MMP of nanoconfined CO2/shale oil/surfactant systems. Validations against experimental data show a deviation of 2.98 % in the CO2 MMP. The MMPs under nanoconfinement are found to be significantly lower than those in bulk phase conditions (up to 22.94 %). The simulation results reveal that decreasing pore size can enhance the miscibility of CO2 and oil by increasing the CO2 adsorption ratio, improving CO2-surfactant interactions, and inhibiting the tendency of CO2 molecules to self-aggregate. The enhancement of CO2-oil miscibility caused by surfactants is ranked by CFP > SF > SDS according to the mixing degrees (Dmix) and the spatial distribution of CO2 around surfactant molecules. In addition, pore type exhibits various abilities in influencing the MMP, owing to their different mineral surface properties and ability to influence CO2-surfactant interactions. Nanopores with stronger hydrophobicity and a denser CO2 distribution around surfactant molecules have lower MMPs. The results show that the order of MMP in terms of pore types is Quartz < Kaolinite < I/M clay. This study elaborates the micro-mechanisms of surfactant-assisted CO2-oil miscibility under nanoconfinement, offering valuable insights for effectively designing CO2 miscible flooding in shale oil reservoir development.

Study on performance regulation of electro-mechanical properties 3D printed BaTiO3/HA porous structure composite ceramic

BaTiO3/Ca10(PO4)6(OH)2 composite ceramic is an outstanding representative of piezoelectric biomaterials, with excellent biocompatibility and piezoelectric effect, and has potential applications in the field of bone tissue repair. In this work, vat photopolymerization 3D printing technology was used to fabricate triply periodic minimal surface structure BaTiO3/Ca10(PO4)6(OH)2 composite ceramic bone tissue scaffolds with different pore sizes and porosity, and their mechanical and electrical properties were studied. First, the ceramic slurry configuration process was optimized to obtain a ceramic slurry with high solid content (45 vol%) and excellent rheological properties. Then the effect of sintering temperature on microstructure, relative density, mechanical properties, and electrical properties is discussed. The results show that when sintering at 1300 °C, the BaTiO3/Ca10(PO4)6(OH)2 composite ceramic has the highest relative density (99.18 %), the highest compressive strength (44 MPa), large relative dielectric constant (379–389), and low dielectric loss. The polarization electric field strength of the BaTiO3/Ca10(PO4)6(OH)2 composite ceramic was set to 15 kV/cm through the test of the hysteresis loop. Finally, based on multi-physics coupled finite element simulation, the effects of different porosity and different pore sizes on stress distribution and piezoelectric potential were analyzed, and the relationship between them was explored through experiments. The results show that as the porosity increases and the pore size decreases, the mechanical properties of the scaffold decrease significantly, and its compressive strength ranges between 1.67 and 4.26 MPa; as the porosity increases and the pore size increases, the piezoelectric coefficient (d33) of the scaffold showed a decreasing trend, and its d33 ranged between 2 and 9 pC/N. The mechanical and electrical properties of the scaffold meet the performance requirements of cancellous bone. In summary, this work provides a strategy for the application of customized BaTiO3/Ca10(PO4)6(OH)2 composite ceramic scaffolds in new-generation orthopedic implants.

Fabrication and Customization of Highly Porous PLGA Membranes Utilizing Near‐Field Electrospinning, Thermal Transitions, and Multilayer Strategies

Polymer porous membranes are crucial in various applications, including water filtration, tissue engineering, and drug administration. Conventional far‐field electrospinning (FFES) is widely used for producing polymeric membranes due to its cost‐effectiveness, scalability, and flexibility in using many polymers. However, FFES has limitations in controlling pore form and size, as it produces randomly oriented fibers that lead to inconsistent and noncustomizable pore sizes. To address these limitations, this work combines near‐field electrospinning (NFES) with thermal treatment of polymer fibers and membranes. NFES offers more precise control over fiber placement and alignment, producing well‐defined fiber patterns with consistent and customizable pore sizes without compromising the thickness of membranes. By exploring the interplay between polymer behavior, thermal effects, and capillary action, the differences in pore area under various temperatures and fiber spacings are characterized. Additionally, this study investigates the influence of multilayer infusion on pore size and geometric arrangement by examining multilayer configurations stacked at various angles. The results indicate that increasing the number of layers leads to decreased pore size, while the alignment of infused fibers affects pore shape. This integrated approach enhances control over membrane characteristics, improving the performance and consistency of polymer porous membrane fabrication across various applications.

Study on the condensate gas phase behavior in Nano-porous media

The pore size in shale has reached the nanoscale. The phase behavior of fluids in nanopores deviates from classical theory, making conventional phase theory inapplicable to shale reservoirs. It is thus of great significance to clarify the phase behavior at the nanometer pore scale in shale. Based on the shale reservoir in the Kaybob of the Duvernay shale, Canada, 6 nm and 10 nm cubic model systems were constructed, and a microscopic physical model was prepared included pathways at 10 nm, 40 nm, 500 nm, and micrometer scale. The fluid phase behavior in nanopores was studied using molecular simulations and nanofluidic chip experiments. The results show that during the retrograde condensation process, the condensate gas in small-scale pores condenses first and is less likely to evaporate as the pressure decreases. The conclusions drawn are: (1) In nanopores, the dew point pressure of condensate gas is higher than that of the bulk phase, and the smaller the scale of nanopores, the higher the dew point pressure. (2) The volume ratio of condensate in nanopores is higher, increasing as pore size decreases. (3) The condensation rate of condensate in nanoporous media varies slowly with pressure drop; During evaporation, the condensation rate of condensate in small pores varies more slowly with pressure drop compared to the bulk phase but is faster in large pores.

Long-term durability of iron-rich geopolymer concrete in sulphate, acidic and peat environments

This study assesses the behaviour of iron-rich type F fly ash geopolymer concretes (GC) exposed to simulated sulphate, acidic, and peat environments, typical of those encountered in tropical peatlands. GC and Portland cement (PC) concrete of comparable strengths were exposed to a range of simulated solutions for 18 months, including 5 % magnesium sulphate (MgSO4), 5 % sodium sulphate (Na2SO4), 1 % and 3 % sulfuric acid (H2SO4) and peat. The GC generally outperformed PC in all conditions. The GC showed a significant increase in strength in the first year, along with enhanced durability properties. Microstructural analysis indicated a decrease in total porosity and pore size. This was attributed to continuing geopolymerization leading to the foration of additional N-A-S-H gel, which filled the pores and solidified the concrete matrix. However, compressive strength decreased at 18 months due to crack propagation caused by drying shrinkage. In Na2SO4, GC attained an 8.9 % and 6.3 % increase in compressive strength at 12 and 18 months, respectively, again attributed to ongoing geopolymerization. GC exposed to MgSO4 exhibited a significant decrease in compressive strength of approximately 11 % at 12 months and 19.8 % at 18 months, attributed to the formation of lower-strength M-A-S-H from reaction between MgSO4 and N-A-S-H gel. After 12 months GC exposed to 1 % and 3 % H2SO4 demonstrated a decrease in compressive strength of approximately 1.2 % and 4.5 %, respectively, together with 2 % and 3 % mass loss. Chemical and microstructural data confirmed this strength reduction due to the vulnerability of N-A-S-H to when exposed to H2SO4. GC exposed to peat solution exhibited a 1.25 % increase in compressive strength at 12-month, but a decrease of 11.3 % at 18-month. Microstructural analysis observed a reduction in Na+ within GC matrix, and the presence of gypsum. The reduction in pore sizes and total porosity suggested generation of zeolite crystalline material was contributing to the pore filling.

Design and optimization of pore structure in three-dimensional micro-nano hierarchical SnOx supercapacitor electrodes for enhanced ion diffusion

This paper introduced a novel continuous electrochemical synthesis strategy to address the challenges of slow ion/electron transport rates and low electrode reaction efficiency in Sn-based electrode materials. This approach leveraged the induction and confinement of bubble templates to assist atoms deposition, generating micron-sized tin skeletons. Subsequently, these skeletons were transformed into a secondary nanoporous structure through dissolution-deposition etching effects. From liquid-phase ions to metal skeletons to porous oxides, the sequential material transformations realized the innovative design of three-dimensional (3D) hierarchical structures. This strategy ingeniously exploited the diffusion advantages of the electrolyte in the micro-nano hierarchical structure to achieve the diffusion enhancement of ions, thus solving the “dead surface” problem in the energy storage process. This study revealed the thermodynamic and kinetic feasibility of the constructed 3D micro-nano hierarchical structure through electrochemical evaluations and theoretical calculations, and elucidated the constitutive relationship in which the electrochemical performance of the electrode materials was enhanced with decreasing pore size. In addition, design optimization of pore structures and modelling exploration of pore size limit values were conducted based on density functional theory (DFT) simulations. These simulations demonstrated the advantages of hierarchical structures with controllable pore sizes in facilitating electrolyte ion diffusion, predicting an optimal pore size of 55 μm for 3D hierarchical porous SnOx electrodes. The integration of this innovative structural design with simulation insights offered significant implications for enhancing the sluggish electrode reaction kinetics of metal oxide electrode materials, advancing the controllable fabrication of high-performance energy storage devices.

Polylactic acid-based composite filter with multi-gradient structure developed for high-efficiency particulate matter filtration and NH3 purification

Particulate matter (PM), ammonia (NH3) and other polluted gases emitted from animal feeding operations have emerged as significant risks to workers, surrounding residents, and the regional environment. Therefore, the development of air filters capable of simultaneously filtering PM and adsorbing toxic gases is particularly important. In this study, a three-layer gradient structure nanofiber filter was prepared by electrospinning technology, consisting of fluorinated Polylactic acid (PLA)/SiO2 as the outer layer, PLA nanofibers as the middle layer, and PLA/UiO-66-NH2 as the inner layer. This gradient structure of composite filter featured gradually decreasing pore sizes, exhibited optimal air filtration performance compared to PLA filter and commercial glass fiber filter. At 5.3 cm/s flow rate, the composite nanofiber filter achieved high filtration efficiency (99.15 % for PM0.5) and low pressure drop (89.65 Pa). Furthermore, the composite nanofiber filter exhibited highest dust holding capacity, indicating longer service life. It also featured excellent self-cleaning capabilities, allowing for reuse after simple water rinsing. Additionally, the results of ammonia (NH3) adsorption tests demonstrated the prepared composite filter’s highest adsorption capacity for NH3. Therefore, this work enhanced the application potential of high-performance air filters in the removal of PM pollution and hazardous gases.

Effect of metakaolin on the chloride diffusion properties of alkali-activated slag in an acidic environment

Alkali-activated materials (AAMs) have good resistance to chemical corrosion compared to silicate cements, but the effect of the pH of chloride-containing solutions on the resistance of AAMs to chloride diffusion is not clear. In this paper, the resistance of alkali-activated slag (AAS) with different metakaolin replacement rate to chloride diffusion in HCl/NaCl solution was investigated in terms of mechanical properties, hydration product composition and pore structure. The experimental results show that acidic solutions lead to alkali leaching, and dissolution of gel and hydrotalcite. The capillary pores that appeared in the AAS after the replacement rate of 10% metakaolin resulted in a decrease in the average pore size of the AAS and low depth of chloride diffusion. 30% metakaolin replacement led to a decrease in the diffusion resistance. In HCl solution, the high [AlO4]5− retention corroded layer was observed in the AAS with 30% metakaolin replacement and this layer slowed down the migration rate of [Cl−]. This study shows the promising application of alkali-activated slag/metakaolin in complex chloride solution environments.

3D chitosan/hydroxyapatite scaffolds containing mesoporous SiO2-HA particles: A new step to healing bone defects

Biocompatible scaffolds with high mechanical strengths that contain biodegradable components could boost bone regeneration compared with nondegradable bone repair materials. In this study, porous chitosan (CS)/hydroxyapatite (HA) scaffolds containing mesoporous SiO2-HA particles were fabricated through the freeze-drying process. According to field emission scanning electron microscopy (FESEM) results, combining mesoporous SiO2-HA particles in CS/HA scaffolds led to a uniform porous structure. It decreased pore sizes from 320 ± 1.1 μm to 145 ± 1.4 μm. Moreover, the compressive strength value of this scaffold was 25 ± 1.2 MPa. The in-vitro approaches exhibited good sarcoma osteogenic cell line (SAOS-2) adhesion, spreading, and proliferation, indicating that the scaffolds provided a suitable environment for cell cultivation. Also, in-vivo analyses in implanted defect sites of rats proved that the CS/HA/mesoporous SiO2-HA scaffolds could promote bone regeneration via enhancing osteoconduction and meliorating the expression of osteogenesis gene to 19.31 (about 5-fold higher compared to the control group) by exposing them to the bone-like precursors. Further, this scaffold's new bone formation percentage was equal to 90 % after 21 days post-surgery. Therefore, incorporating mesoporous SiO2-HA particles into CS/HA scaffolds can suggest a new future tissue engineering and regeneration strategy.