Microscale Pores Research Articles

Investigation of cracking behavior of fine-grained clays exposed to different humidity environments and engineering implications based on X-ray computed tomography

Due to the humidity difference between fine-grained clay and atmosphere environment, the complex crack network is formed, which is the main channel for water storage and migration and hence poses a potential threat to engineering construction. Therefore, the appropriate characterization of cracking behavior of fine-grained clay is of great significance for exploring its microphysical properties. To this end, this work took expansive soils as research object and a series of desiccation tests and X-ray computed tomography tests were conducted to investigate the shrinkage cracking behavior. The results indicate that a higher desiccation rate records a smaller shrinkage strain, but it aggravates the cracking on a much larger scale. Especially at high desiccation rates, two-dimensional crack ratio shows a significant fluctuation. Small cracks tend to turn into large ones during desiccation, and the increasing desiccation rate primarily exerts a significant effect on the cracks with equivalent radius more than 1000 µm. The expansive soil is dominated by horizontal cracks, and a low desiccation rate mainly promotes the connection between horizontal cracks, whereas high desiccation rates enhance the connectivity of oblique cracks, which exerts an adverse effect on soil slopes. Besides, the rise in desiccation rate leads to a wealth of micro-scale pores and throats occurring in the soil. The fine-grained clays at higher desiccation rates present larger pore and throat volume, more connected pores, and higher average coordination number, thus enhancing the connectivity between pore and pore. Permeability simulation results also confirm the positive correlation between connected crack ratio and hydraulic conductivity of the soil. In terms of engineering significance, narrowing down the difference in humidity between fine-grained clays and atmosphere is the most effective measure to constrain the extension of cracks.

Laser powder bed fusion printed poly-ether-ether-ketone/bioactive glass composite scaffolds with dual-scale pores for enhanced osseointegration and bone ingrowth

Although poly-ether-ether-ketone (PEEK) implants hold significant medical promise, their bioinert nature presents challenges in osseointegration and bone ingrowth within clinical contexts. To mitigate these challenges, the present study introduces Diamond PEEK/bioactive glass (BG) composite scaffolds, characterized by macro/micro dual-porous structures, precisely fabricated via laser powder bed fusion (LPBF) technology. The findings indicate that an increase in BG content within these scaffolds significantly augments their hydrophilicity and hydroxyapatite formation capacities. Stress-strain curve analysis demonstrates reliable load-bearing stability across all scaffold types. In vitro assessments confirmed the non-cytotoxicity of PEEK/BG samples and demonstrated improved osteogenic differentiation and mineralization with increased BG incorporation. Further, in vivo experiments illustrated that the Diamond porous structure of these scaffolds facilitated bone growth, an effect notably amplified with higher BG content. Particularly in groups with 15 wt% and 25 wt% BG scaffolds, new bone formation was observed not only within the macropores of the Diamond structure but also within the micropores inside the scaffold rod, suggesting an almost seamless fusion with the new bone. This demonstrates the scaffolds’ effective osteointegration and bone ingrowth properties. This study conclusively established the effectiveness of Diamond-structured PEEK/BG composite scaffolds, fabricated via LPBF, in bone repair. It highlights the crucial role of BG in enhancing osteogenic potential through interaction with the macro/micro pores of the scaffold. Statement of significanceThis study addresses the bioinert nature of PEEK implants by developing Diamond-structured PEEK/bioactive glass (BG) composite scaffolds by laser powder bed fusion. The dual-porous macro/microstructure enhances hydrophilicity and hydroxyapatite formation, vital for bone regeneration. By adjusting the BG content, we controlled the melt viscosity and sintering rate, leading to the formation of beneficial microscale pores. These pores resolve the issue of ineffective bioactive fillers in previous LPBF-fabricated scaffolds, enhancing the osteogenic potential of BG and inducing superior bone ingrowth and osseointegration. In vitro and in vivo analyses show enhanced osteogenic differentiation, mineralization, and bone growth, underscoring the clinical potential of these scaffolds for bone repair.

Laser‐Induced Formation of Fine Porous Graphitic Carbon for Eco‐Friendly Supercapacitors

An electric double‐layer capacitor (EDLC), which is one of the pivotal energy storage devices, provides rapid charge–discharge capabilities and an extended cycle life. Areal capacitance, a key indicator of EDLC performance, increases with the specific surface area of its electrodes. This study demonstrates a method for significantly increasing the specific surface area in the laser‐induced graphitization of biodegradable polymers by incorporating NaHCO3 into the composite sheet, generating not only microscale pores but also a large number of nanoscale fine pores. Furthermore, it shows that using these structures as EDLC electrodes leads to a substantial increase in areal capacitance. An increase in the number of fine pores formed in the structure and a corresponding rise in the areal capacitance of the fabricated EDLC are observed with the increase in the NaHCO3 weight ratio. Notably, the composite sheets are composed of natural‐derived, biodegradable materials, while NaHCO3 is known for its low corrosivity and biotoxicity. The proposed method thus offers a pathway for fabricating energy storage devices with minimal environmental impact, ensuring their eco‐friendly disposal post‐use.

Thylakoid-based green preparation of porous microneedles for antibiotic residues detection in food samples

BackgroundAntibiotic residues in food chain have raised concerns regarding their toxicity and involvement in antimicrobial resistance. However, most existing antibiotic biosensors are primarily applicable to liquid food samples. Given the complex matrix characteristics of foods, there is an urgent need for the development of effective antibiotic detection platforms that exhibit high universality and flexibility. Porous microneedles (PMN) are microdevice structures with needle-like shapes and microscale pores throughout their composition, which facilitate rapid sampling. Consequently, the integration of PMN with biosensors holds significant promise for the detection of antibiotic residues in complex food samples. ResultsIn this study, hydrogel-forming PMN are fabricated by leveraging the oxygen-production capacity of thylakoid to generate bubbles and form porous structures. These PMN are then integrated with a fluorescence aptasensor for the quantification of the antibiotic netilmicin. The aptasensor consists of a netilmicin (NET) aptamer with stem loop and hairpin structure, which facilitated the binding of SYBR Green I to produce a fluorescent signal. In the presence of NET, the complete binding between NET and the aptamer results in a reduction of fluorescence intensity, thereby generating a detectable signal change for the detection of NET. Utilizing capillary action accelerate fluid extraction (2.9 times faster than nonporous microneedles) and a large specific surface area (5.1072 m2/g) conducive to aptasensor adsorb, the PMN achieve efficient capture and quantification of antibiotic with limits of detection and quantitation of 5.99 nM and 19.8 nM, respectively. SignificancePorous microneedles with tunable porosity and desirable mechanical properties are successfully fabricated. The integration of PMN with aptasensor enable the efficient detection of netilmicin in fish, milk and river water samples, demonstrating high recovery rates. The PMN represent potential tools for the convenient and rapid detection of antibiotic residues within complex food matrices, thereby enhancing food safety monitoring.

Numerical study of transpiration cooling at different outlet angles and hole pattern

The effects of transpiration cooling depends on the distribution of micropores in porous materials. The work simplifies the porous medium to a micro-scale pore plate structure that is densely organized, based on the idea of the capillary bundle model. The effects of hole pattern and hole outlet angle on transpiration cooling are investigated using numerical simulation. It is discovered that the hole outlet angle mostly affects the homogeneity of temperature distribution and has minimal effect on the surface cooling efficiency. The temperature uniformity index dropped by 35.9% yet the surface cooling efficiency only declined by 1.1% when the outlet angle was lowered from 45° to −45°. Furthermore, the temperature uniformity and cooling efficiency are directly affected by the hole pattern. When the long axis of the elliptical hole is parallel to the mainstream, it can achieve the best temperature uniformity; however, when the long axis is perpendicular to the mainstream direction, it can achieve higher cooling efficiency. Third, the material’s permeability will be decreased to varying degrees depending on the hole pattern and hole outlet angle. The results have important reference significance for the design of porous materials used for transpiration cooling.

Enhanced Electromagnetic Interference Shielding Properties of CNT/Carbon Composites by Designing a Hierarchical Porous Structure.

With the widespread use of electronic devices, electromagnetic interference (EMI) has become an increasingly severe issue, adversely affecting device performance and human health. Carbon nanotubes (CNTs) are recognized for their electrical conductivity, flexibility, and stability, making them promising candidates for EMI shielding applications. This research developed hierarchical porous-structured CNT/carbon composites for enhancing electromagnetic interference (EMI) shielding properties. Featuring a CNT film with nano-scale pores and an amorphous carbon layer with micro-scale pores, the CNT/carbon composites are strategically arranged to promote the penetration of EM waves into the composite's interior and facilitate multiple reflections, thereby improving the EMI shielding performance. An impressive EMI shielding effectiveness of 61.4 dB was achieved by the CNT/carbon composites, marking a significant improvement over the 36.5 dB measured for the pristine CNT film. Owing to the micro pores in the amorphous carbon layer, a notable reduction in the reflection shielding efficiency (SER) but, concurrently, a substantial increase in the absorption shielding efficiency (SEA) compared with the pristine CNT film was realized in the composites. This study successfully validated the effectiveness of the hierarchical porous structure in enhancing the EMI shielding performance, providing a promising new strategy for the development of lightweight, flexible, and efficient EMI shielding materials.

Conformational interlocking induced construction of hierarchically porous graphene membrane for ultrahigh-pressure sensing

Based on microstructure engineering, graphene oxide (GO)-based piezoresistive pressure sensors have attracted increasing attention due to its amazing sensitivities, but the point-to-point contact mechanism among nanosheets compromises their high-pressure monitoring capabilities. Inspired by the multiple conformations of GO nanosheets, we utilize π-π conjugated interlayer interactions to lock the 3D crumpled conformation of nanosheets, resulting in controllable assembly into a flexible graphene membrane with hierarchically porous structures (PGM). These designed structures include microscale pores formed by the loose stacking of 3D crumpled nanosheets and nanoscale pores supported by densely packed crumples, reaching up to 100 nm in height. The PGM flexible sensor exhibits an unprecedented ultrahigh-pressure response of up to 2000 kPa, with high sensitivities of 1.1 and 0.7 kPa−1 in the pressure ranges of 1–600 kPa and 600–2000 kPa, respectively, and demonstrates over 10,000 cycles of high-pressure stability. Moreover, the PGM flexible sensors enable real-time monitoring of pressure vessel inflation/deflation processes and human activities such as finger, elbow, and knee bending, as well as walking, running, and jumping. This hierarchically porous structure provides a promising avenue for ultra-wide-range and ultra-high-pressure sensing devices, with potential applications in structural health monitoring, personal healthcare, and medical diagnostics.

Phase Transition Characteristics of Hydrate Formation Process in Microscale Pores

Phase Transition Characteristics of Hydrate Formation Process in Microscale Pores

Experimental study on the influence of external fluids on the pore structure of carbonaceous shale

Shale reservoirs have complex mineral compositions and are rich in micro-scale pores. It is of great scientific and engineering significance to explore the mechanism of external fluids on the pore throat structure of shale. In this paper, pure carbonaceous shale is taken as the research object, and the mechanism of the influence of slip water and reflux fluid on the pore throat structure is analyzed by using nuclear magnetic resonance (NMR) technology. Then, the sensitivity of different types of shale to external fluids is comparatively analyzed and summarized. The results show that (1) the oil slick has a certain effect on the total porosity of different types of shale. The rate of change is shown as carbonaceous shale (− 7.1%) > pure shale (− 1.6%). (b) For slickwater, the average reduction of macro- and micro/nanopores in carbonaceous shale is 90.0% and 5.0%, respectively, while the average reduction of macro- and mesopores in pure shale is 17.7% and 6.8%, respectively. (c) Total porosity of different shale types is insensitive to refluxing fluids. The average increase in macro-, meso-, and small pores of carbonaceous shale is 31.8%, 23.6%, and 20.2%, respectively; the average increase in macro- and small pores of pure shale is 17.1%.

Tungsten Strongly Inhibits Sintering of Porous Iron During High-Temperature Redox Cycling.

Freeze-cast Fe-25W (at%) lamellar foams show excellent resistance to degradation at 800°C during steam-hydrogen redox cycling between the metallic and oxide states, with fast reaction kinetics maintained up to at least 100 redox cycles with full Fe utilization. This very high stability stems from the sintering inhibition of W combined with the freeze-cast architecture and the chemical vapor transport (CVT) mechanism of reduction. These three factors create a hierarchical porosity in the foam, consisting of i) macroscopic elongated channels, ii) micro-scale sintering inhibition pores, and iii) submicron CVT pores. Microstructural characterization via SEM and EDS is combined with in situ XRD to fully explore the phase evolution and microstructural impact of W on Fe during redox cycling. Comparison with tapped Fe-25W (at%) powder beds reveals that the freeze-cast channels and lamellae are not critical to the performance of the material.

Mechanical Performance Optimization and Microstructural Mechanism Study of Alkali-Activated Steel Slag–Slag Cementitious Materials

The optimal proportion of alkali-activated steel slag–slag cementitious materials is investigated by considering the combined effects of steel slag content, alkali content, water glass modulus, and water–binder ratio using the Box–Behnken design in response surface methodology. Qualitative and semi-quantitative analyses of X-ray diffraction (XRD) patterns and scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS) images are conducted. The microstructural mechanism is elucidated based on the chemical composition, surface morphology, and microscale pore (crack) structures of the samples. A microreaction model for the alkali-activated steel slag and slag is proposed. The optimal composition for alkali-activated steel slag–slag cementitious materials is as follows: steel slag content, 38.60%; alkali content, 6.35%; water glass modulus, 1.23; and water–binder ratio, 0.48. The strength values predicted by the response surface model are p1d = 32.66 MPa, p7d = 50.46 MPa, and p28d = 56.87 MPa. XRD analysis confirms that the compressive strength of the sample is not only influenced by the amount of gel formed, but also, to a certain extent, by the CaCO3 crystals present in the steel slag, which act as nucleation sites. The SEM-EDS results confirm that the gel phase within the system comprises a hydrated calcium silicate gel formed through the reaction of volcanic ash and geopolymer gel formed through geo-polymerization. Analysis of the pore (crack) structure reveals that the compressive strength of the specimens is primarily influenced by porosity, with a secondary influence of the pore fractal dimension.

Synthesis of micro/nano multi-scale polyimide aerogels via confinement-controlled freeze-casting

The freeze-casting is widely utilized as a tool for regulating micro-scale pore structures in the fabrication of flexible polyimide (PI) aerogels for applications in adsorption, filtration, and fire-retardant. Herein, a confinement-controlled freeze-casting method is developed to fabricate PI aerogels with excellent thermal insulation properties by designing multi-scale structural adaptability. In a confinement-controlled system, the enhanced solid/solid and solid/liquid interface interactions in the solution dispersion system induce dendritic evolution of ice crystals. Under the directional freezing, grown dendritic ice crystals squeeze the loaded particles to form polyamic acid salt (PAAs) cryogels. Followed by template removal and thermal imidization, PI aerogels with a micro/nano-scale slit-like porous structure were obtained. The PI aerogels are characterized by ultra-low density (as low as 9.82 mg/cm3) and exceptional thermal insulation performance (25.0 mW/(m·K) at 25 °C).

A novel reservoir classification method for sandstone reservoir evaluation using multi-scale digital rock method

The formulation of an effective development plan, optimizing exploitation efficiency, relies heavily on accurate reservoir characterization. However, existing reservoir classification methodologies, which rely on macroscopic geological observations and well-logging data, have limitations in data availability and fail to capture micro-scale pore structure characteristics accurately. The emerging technology of digital rock, widely employed in the petroleum industry, also faces challenges in accurately capturing reservoir heterogeneity due to its single-scale nature and limited application for reservoir classification. To overcome these challenges, this study presents an innovative reservoir classification approach based on the multi-scale digital rock method. This approach integrates qualitative assessment of micro-CT images for particle contact relationships and pore types with quantitative evaluation of multi-scale characteristic parameters, obtained from micro-CT and scanning electron microscopy (SEM) images. The proposed classification method demonstrates excellent agreement with the prioritization of development and production data for offshore sandstone reservoirs. By establishing a robust evaluation methodology, this classification method facilitates exploration potential assessment and development strategy optimization within the field.

An Experimental Investigation into the Role of an In Situ Microemulsion for Enhancing Oil Recovery in Tight Formations

Surfactant huff-n-puff (HnP) has been shown to be an effective protocol to improve oil recovery in tight and ultratight reservoirs. The success of surfactant HnP for enhanced oil recovery (EOR) process depends on the efficiency of the designed chemical formula, as the formation of an in situ microemulsion by surfactant injection is considered to be the most desirable condition for achieving an ultra-low interfacial tension during the HnP process. In this work, we conducted experimental studies on the mechanism of in situ microemulsion EOR in the Mahu tight oil reservoir. Salinity scan experiments were carried out to compare different surfactants with crude oil from the Mahu reservoir, starting with the assessment of surfactant micellar solutions for their ability to form microemulsions with Mahu crude oil and examining the interfacial characteristics. Subsequently, detailed micromodels representing millimeter-scale fractures, micron-scale pores, and nano-scale channels were utilized to study the imbibition and flowback of various surfactant micellar solutions. Observations of the in situ microemulsion system revealed the mechanisms behind the enhanced oil recovery, which was the emulsification’s near-miscibility effect leading to microemulsion formation and its performance under low-interfacial-tension conditions. During the injection process, notable improvements in the micro-scale pore throat heterogeneity were observed, which improved the pore fluid mobility. The flowback phase improved the channeling between the different media, promoting a uniform movement of the oil–water interface and aiding in the recovery of a significant amount of the oil phase permeability.

Vat photopolymerization of dual-scale porosity alumina honeycombs using phase-separable camphene porogen dissolved in binary photopolymer blends

Dual-scale porosity ceramics comprised of macro-scale pore networks surrounded by porous frameworks manufactured by additive manufacturing (AM) can offer significantly enhanced functions compared to conventional porous ceramics. However, exploring new ways of more tightly controlling micro-scale porous structures for AM still remains challenging. Here, we propose a novel type of vat photopolymerization using camphene as a phase-separable porogen dissolved in binary photopolymer blends for manufacturing dual-scale porosity alumina honeycombs. More specifically, solid camphene with various contents (40 vol%, 50 vol%, and 60 vol%) could be completely dissolved in blends of triethylene glycol dimethacrylate (TEGDMA) and polyethylene glycol diacrylate (PEGDA) used as solvent and anti-solvent, respectively, at room temperature and then crystallize dendritically at ∼ 5 °C via phase separation. After which, thin layers of phase-separated alumina suspensions could be selectively photopolymerized by a digital light processing (DLP) engine to construct 3-dimensionally interconnected macro-scale pore channels. In addition, micro-scale pores could be created in alumina frameworks by removing camphene-rich crystals by freeze-drying. This new approach enabled manufacturing of well-defined macro-scale honeycomb structures with tailored micro-scale porosities. As the camphene content increased from 40 vol% to 60 vol%, micro-scale porosity increased from 39.1 ± 0.5 vol% to 57.5 ± 0.6 vol%, and thus the overall porosity increased from 58.5 ± 0.1 vol% to 68.8 ± 0.3 vol%, while the compressive strength decreased from 355.6 ± 67.1 MPa to 97.6 ± 10.2 MPa.

Evolution of pore structure and reactive transport parameters during acid leaching of sandstone uranium ore

The changes in the micro-scale pore structure during the acid leaching of sandstone uranium ore significantly affect its reactive transport parameters, which, in turn, directly influence the leaching efficiency of uranium. Consequently, understanding and managing the dynamic evolution of the pore structure of sandstone at micro-scale during acid leaching is beneficial for enhancing the leaching efficiency of uranium. This paper employs a dynamic continuous water-rock reaction experiment on sandstone uranium ore to simulate the in-situ acid leaching process. Additionally, X-ray micro-computed tomography (μCT) scanning was utilized to produce three-dimensional (3D) images at various leaching stages. Subsequently, image processing techniques were employed to characterize and parameterize the pore structure within these images. The results revealed that, during the leaching process, mineral dissolution led to an increase in the interconnected pores, while there was a decrease in the isolated pores. Nonetheless, at the leading edge of the sandstone uranium ore, detachment of mineral grains occurred during the leaching process along the direction of fluid flow. The migration of mineral grains resulted in a reduction of interconnected pores and an increase in the isolated pores. The analysis of 3D images indicated that porosity, permeability, the percentage of connected pore area and the reactive surface area exhibited similar variation trends throughout the leaching process. Furthermore, the permeability, the percentage of connected pore area and the reactive surface area displayed a positive correlation with porosity. The study holds valuable insights to develop a deeper understanding of the evolutionary patterns regarding the pore structure during the in-situ acid leaching of sandstone uranium ore.

Microscale advection governs microbial growth and oxygen consumption in macroporous aggregates.

Most microbial life on Earth is found in localized microenvironments that collectively exert a crucial role in maintaining ecosystem health and influencing global biogeochemical cycles. In many habitats such as biofilms in aquatic systems, bacterial flocs in activated sludge, periphyton mats, or particles sinking in the ocean, these microenvironments experience sporadic or continuous flow. Depending on their microscale structure, pores and channels through the microenvironments permit localized flow that shifts the relative importance of diffusive and advective mass transport. How this flow alters nutrient supply, facilitates waste removal, drives the emergence of different microbial niches, and impacts the overall function of the microenvironments remains unclear. Here, we quantify how pores through microenvironments that permit flow can elevate nutrient supply to the resident bacterial community using a microfluidic experimental system and gain further insights from coupled population-based and computational fluid dynamics simulations. We find that the microscale structure determines the relative contribution of advection vs diffusion, and even a modest flow through a pore in the range of 10 µm s-1 can increase the carrying capacity of a microenvironment by 10%. Recognizing the fundamental role that microbial hotspots play in the Earth system, developing frameworks that predict how their heterogeneous morphology and potential interstitial flows change microbial function and collectively alter global scale fluxes is critical.IMPORTANCEMicrobial life is a key driver of global biogeochemical cycles. Similar to the distribution of humans on Earth, they are often not homogeneously distributed in nature but occur in dense clusters that resemble microbial cities. Within and around these clusters, diffusion is often assumed as the sole mass-transfer process that dictates nutrient supply and waste removal. In many natural and engineered systems such as biofilms in aquatic environments, aggregates in bioremediation, or flocs in wastewater treatment plants, these clusters are exposed to flow that elevates mass transfer, a process that is often overlooked. In this study, we show that advective fluxes can increase the local growth of bacteria in a single microenvironment by up to 50% and shape their metabolism by disrupting localized anoxia or supplying nutrients at different rates. Collectively, advection-enhanced mass transport may thus regulate important biogeochemical transformations in both natural and engineered environments.

Microstructure, Mechanical Property and Thermal Conductivity of Porous TiCO Ceramic Fabricated by In Situ Carbothermal Reduction of Phenolic Resin and Titania.

The porous TiCO ceramic was synthesized through a one-step sintering method, utilizing phenolic resin, TiO2 powder, and KCl foaming agent as raw materials. Ni(NO3)2·6H2O was incorporated as a catalyst to facilitate the carbothermal reaction between the pyrolytic carbon and TiO2 powder. The influence of Ni(NO3)2·6H2O catalyst content (0, 5, 10 wt.% of the TiO2 powder) on the microstructure, compressive strength, and thermal conductivity of the resultant porous TiCO ceramic was examined. X-ray diffraction and X-ray photoelectron spectroscopy results confirmed the formation of TiC and TiO in all samples, with an increase in the peak of TiC and a decrease in that of TiO as the Ni(NO3)2·6H2O content increased from 0% to 10%. Scanning electron microscopy results demonstrated a morphological change in the pore wall, transforming from a honeycomb-like porous structure composed of well-dispersed carbon and TiC-TiO particles to rod-shaped TiC whiskers, interconnected with each other as the catalyst content increased from 0% to 10%. Mercury intrusion porosimetry results proved a dual modal pore-size distribution of the samples, comprising nano-scale pores and micro-scale pores. The micro-scale pore size of the samples minorly changed, while the nano-scale pore size escalated from 52 nm to 138 nm as the catalyst content increased from 0 to 10%. The morphology of the pore wall and nano-scale pore size primarily influenced the compressive strength and thermal conductivity of the samples by affecting the load-bearing capability and solid heat-transfer conduction path, respectively.

Electrochemical performance enhanced by solvent infiltration strategy to increase micro-mesopores within wood tracheid walls

The utilization of wood-derived carbon thick electrodes has demonstrated remarkable structural advantages in the realm of electrochemical energy storage and catalysis. Its exceptional structural stability, mechanical strength, and well-organized pore structure position it as a promising material for self-supporting electrodes. The multi-scale cross-linking of lignin, cellulose, and hemicellulose within the wood tracheid wall establishes a convenient prerequisite for structural modification. However, the significance of dynamic nanopores on wood tracheid walls in enhancing the microporous/mesoporous structure of wood-derived carbon electrodes has been overlooked due to the focus on operability of microscale array pores and wood decomposition processes. Here, we employ a straightforward, highly efficient, and environmentally sustainable solvent infiltration strategy to enhance the nanopore content within the wood tracheid wall, ultimately resulting in a significant enhancement of the microporous/mesoporous composition within the wood-derived electrode. The charge storage capacity of wood-derived carbon electrode is doubled through the implementation of a solvent permeation modification strategy, while its abundant micro/mesoporous structure also endows it with significant potential in the field of electrocatalysis. Therefore, this thermal and solvent permeation modification strategy is anticipated to supplant the conventional acid-base etching method and offer a novel research concept for the advancement of wood-based carbon electrodes with abundant pore structure and exceptional electrochemical properties.

Achieving strong interfacial bonding of CFRP and magnesium alloy by modifying magnesium alloy surface via alkaline etching with EDTA addition

The interfacial properties of fibre metal laminates are closely related to the surface microstructure of metals. Herein, a hitherto unreported honeycomb-like micro/nano-porous structure was successfully fabricated on an AZ31B Mg alloy surface by incorporation of ethylenediaminetetraacetic acid disodium (EDTA-2Na) into an alkaline solution and achieved excellent interfacial bonding property between AZ31B and carbon fibre-reinforced plastic. The addition of EDTA-2Na can promote the formation of etched pores. The growing nano-scale etched pores join together to produce micro-scale pores and ultimately lead to the formation of a micro/nano-porous structure. The 60 min etched AZ31B/carbon fibre-reinforced plastic laminate exhibits a bonding strength of 25.87 MPa, which is an increase of 350.7% compared to that of the untreated sample. The significant increase in bonding strength is mostly ascribed to composite mechanical interlocking by the micro/nano-porous structure and chemical bonding through the formation of MgCO3 and MgO1+X. In addition, the characteristics of micro-pores also affect the bonding strength.