Large Pore Research Articles

2D Conjugated Metal–Organic Frameworks Bearing Large Pore Apertures and Multiple Active Sites for High‐Performance Aqueous Dual‐Ion Batteries

2D conjugated metal–organic frameworks (2D c‐MOFs) with large pore sizes and high surface areas are advantageous for adsorbing iodine species to enhance the electrochemical performance of aqueous dual‐ion batteries (ADIBs). However, most of the reported 2D c‐MOFs feature microporous structures, with few examples exhibiting mesoporous characteristics. Herein, we developed two mesoporous 2D c‐MOFs, namely PA‐TAPA‐Cu‐MOF and PA‐PyTTA‐Cu‐MOF, using newly designed arylimide based multitopic catechol ligands (6OH‐PA‐TAPA and 8OH‐PA‐PyTTA). Notably, PA‐TAPA‐Cu‐MOF exhibits the largest pore sizes (3.9 nm) among all reported 2D c‐MOFs. Furthermore, we demonstrated that these 2D c‐MOFs can serve as promising cathode host materials for polyiodides in ADIBs for the first time. The incorporation of triphenylamine moieties in PA‐TAPA‐Cu‐MOF resulted in a higher specific capacity (423.4 mAh g‐1 after 100 cycles at 1.0 A g‐1) and superior cycling performance, retaining 96% capacity over 1000 cycles at 10 A g‐1 compared to PA‐PyTTA‐Cu‐MOF. Our comparative analysis revealed that the increased number of N anchoring sites and larger pore size in PA‐TAPA‐Cu‐MOF facilitate efficient anchoring and conversion of I3‐, as supported by spectroscopic electrochemistry and density functional theory calculations.

2D Conjugated Metal-Organic Frameworks Bearing Large Pore Apertures and Multiple Active Sites for High-Performance Aqueous Dual-Ion Batteries.

2D conjugated metal-organic frameworks (2D c-MOFs) with large pore sizes and high surface areas are advantageous for adsorbing iodine species to enhance the electrochemical performance of aqueous dual-ion batteries (ADIBs). However, most of the reported 2D c-MOFs feature microporous structures, with few examples exhibiting mesoporous characteristics. Herein, we developed two mesoporous 2D c-MOFs, namely PA-TAPA-Cu-MOF and PA-PyTTA-Cu-MOF, using newly designed arylimide based multitopic catechol ligands (6OH-PA-TAPA and 8OH-PA-PyTTA). Notably, PA-TAPA-Cu-MOF exhibits the largest pore sizes (3.9 nm) among all reported 2D c-MOFs. Furthermore, we demonstrated that these 2D c-MOFs can serve as promising cathode host materials for polyiodides in ADIBs for the first time. The incorporation of triphenylamine moieties in PA-TAPA-Cu-MOF resulted in a higher specific capacity (423.4 mAh g-1 after 100 cycles at 1.0 A g-1) and superior cycling performance, retaining 96% capacity over 1000 cycles at 10 A g-1 compared to PA-PyTTA-Cu-MOF. Our comparative analysis revealed that the increased number of N anchoring sites and larger pore size in PA-TAPA-Cu-MOF facilitate efficient anchoring and conversion of I3-, as supported by spectroscopic electrochemistry and density functional theory calculations.

An initial study of cell separation based on mechanical properties using a sponge-like monolithic polymer

We developed a novel cell separation method based on the mechanical properties using a sponge-like monolithic polymer (SPM) in a spin-column format capable of high throughput and mass processing for cell diagnosis and separation. The continuous large flow pores of the monolithic skeleton around 200 μm were expected to act as a sieving matrix for large flexible molecules such as cells larger than 10 μm in diameter, based not only on the size but also on the mechanical deformability of the cells. The passage rates of rigid polystyrene beads ranging in size from 1 to 10 μm were investigated and demonstrated that the spin column acted as a separation matrix rather than a size-based cut-off filter in the 60 and 200 μm pores of the SPM. Two cell types, adherent cells (HeLa cells) and suspension cells (THP-1 cells), showed different passage behavior in the spin column, and 70 % and 30 % of the cells, respectively, were trapped in the column and never eluted. To investigate how the mechanical deformability of the cells affects the passage behavior, glutaraldehyde treatment, which denatured the proteins and changed the elastic moduli, was performed and compared. As a result, the fixed cells drastically reduced the passage rate and became trapped inside the SPM column. These initial studies explored a new application field of SPM for high throughput cell separation based on the mechanical properties of the cells despite the same size, and contribute to a new cell assay method prior to cell transplantation.

How Does the Antibiotic Amphotericin B Enter Membranes and What Does It Do There?

Amphotericin B is a popular antifungal antibiotic, but the exact way it works is still a matter of debate. Here, we used monolayers composed of phosphatidylcholine with ergosterol as a model of fungal lipid membranes to study drug incorporation from the aqueous phase and analyze the molecular reorganization of membranes underlying the biological activity of the antibiotic. The results show that the internalization of antibiotic molecules into membranes occurs only in the presence of ergosterol in the lipid phase. Comparison of images of solid-supported monolayers obtained by atomic force microscopy and lifetime imaging fluorescence microscopy shows the formation of intramembrane clusters of various sizes in the lipid phase, consisting mainly of antibiotic dimers and relatively large membrane pores (∼15 nm in diameter). The results reveal multiple modes of action of amphotericin B, acting simultaneously, each of which adversely affects the structural properties of the lipid membranes and their physiological functionality.

Bimetallic Copper-Cerium-Based Metal-Organic Frameworks for Selective Carbon Dioxide Capture.

Metal-organic frameworks (MOFs) are highly regarded as valuable adsorbent materials in materials science, particularly in the field of CO2 capture. While numerous single-metal-based MOFs have demonstrated exceptional CO2 adsorption capabilities, recent advancements have explored the potential of bimetallic MOFs for enhanced performance. In this study, a CuCe-BTC MOF was synthesized through a straightforward hydrothermal method, and its improved properties, such as high surface area, smaller pore size, and larger pore volume, were compared with those of the bare Ce-BTC. The impact of the Cu/Ce ratio (1:4, 1:2, 1:1, and 3:2) was systematically investigated to understand how adding a second metal influences the CO2 adsorption performance of the Ce-BTC MOF. Various characterization techniques, including scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, thermogravimetric analysis, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and N2 BET surface area analysis, were employed to assess the physical and chemical properties of the bare Ce-BTC and CuCe-BTC samples. Notably, CuCe-BTC-1:2 exhibited superior surface area (133 m2 g-1), small pore size (3.3 nm), and large pore volume (0.14 cm3 g-1) compared to the monometallic Ce-BTC. Furthermore, CuCe-BTC-1:2 demonstrated a superior CO2 adsorption capacity (0.74 mmol g-1), long-term stability, and good CO2/N2 selectivity. This research provides valuable insights into the design of metal-BTC frameworks and elucidates how introducing a second metal enhances the properties of the monometallic Ce-BTC-MOF, leading to improved CO2 capture performance.

Influence of basalt fiber and polypropylene fiber on the mechanical and durability properties of cement-based composite materials

To boost the mechanical strength and endurance quality of cement-based composites, basalt fiber and polypropylene fiber have been included cement-based composites in a single-doped and mixed manner, respectively. Through the tests of flexural strength, compressive strength, drying shrinkage and freeze-thaw cycle, the mechanics properties and endurance quality of cement-based composites with different fiber contents were analyzed. Scanning electron microscopy and a mercury intrusion test were used to compare and study the microstructure and pore structure properties of cement-based composites. The results indicate that the improvement of compressive strength for cement-based composites by single adding basalt, polypropylene fiber and mixed addition of two kinds of fibers is not obvious, but improving the flexural strength of composites by single addition of fiber and 1:1 mixing in a certain dosage range is effective. Among them, 1:1 mixed fiber shows a better advantage superposition effect, which shows better enhancement and toughening effect on composites. Fiber single doping and 1:1 mixing can reduce the Drying shrinkage and mass loss rate of the composites within a certain range, and enhance the composites' ability to resist Drying shrinkage and freezing. Based on the comprehensive mechanical properties and durability tests, it is recommended that the content range of the two fibers mixed with 1:1 is 0.4 %–0.6 %. Both basalt fiber and polypropylene fiber can be closely combined with the cement matrix, and randomly distributed in the composite material to form a network structure, which has the function of series skeleton, effectively inhibits the generation and expansion of cracks in the composite material, and improves the microstructure of the composite material. Both basalt fiber and polypropylene fiber can reduce the harmful pores and multi-harmful pores of the composite material, and transform them into harmless pores and less harmful pores, refine the internal pore structure of the composite material, and improve its compactness. The two kinds of fibers are randomly distributed to form a network structure, which refines the large pore size inside the composite material and blocks the connected pores, and the basalt fiber is refined to fill the interface between the polypropylene fiber and the cement matrix, so that the composite material is more compact, thereby significantly improving the mechanical properties and durability of the composite material.

Formation and evolution of shale overpressure in deep Wufeng-Longmaxi Formation in southern Sichuan basin and its influence on reservoir pore characteristics

In the deep Longmaxi Formation shale gas reservoirs of the southern Sichuan Basin, strong overpressure is universally developed to varying degrees. However, there is currently a lack of in-depth research on the formation mechanisms, evolutionary patterns, and the controlling effects on reservoir pore characteristics of strong overpressure. This limitation significantly restricts the evaluation of deep shale gas reservoirs. This study selected typical overpressured shale gas wells in Yongchuan, Luzhou, and Dazu areas as research subjects. Through comprehensive methods such as log analysis, fluid inclusion analysis, and numerical simulation, the dominant mechanisms of strong overpressure formation were determined, and the pressure evolution from early burial to late strong uplift was characterized. Additionally, the impact of varying degrees of overpressure on reservoir pore characteristics was studied using techniques such as scanning electron microscopy, gas adsorption-mercury intrusion, and helium porosity testing. The research findings indicate that hydrocarbon generation expansion is the primary mechanism for strong overpressure formation. The pressure evolution in the early burial phase is controlled by the processes of kerogen oil generation and residual oil cracking into gas. The reservoir experienced three stages: normal pressure (Ordovician to Early Triassic), overpressure (Early Triassic to Early Jurassic), and strong overpressure (Early Jurassic to Late Cretaceous), with pressure coefficients of approximately 1.08, 1.56, and 2.09, respectively. During the late strong uplift phase, the adjustment of early overpressure occurred due to temperature decrease and gas escape, leading to a decrease in formation pressure from 140.55 MPa to 81.63 MPa, while still maintaining a state of strong overpressure. Different degrees of strong overpressure exert a significant control on the physical properties of shale reservoirs and the composition of organic matter pores. Variations exist in the organic matter pore morphology, structure, and connectivity within the deep Wufeng-Longmaxi shale. Higher overpressure favors the preservation of organic large pores and reservoir porosity. Under conditions of strong overpressure development, deep siliceous shales and organically rich clay shales exhibit favorable reservoir properties. By determining the dominant mechanisms of strong overpressure in the Wufeng-Longmaxi Formation and studying pore characteristics, this research not only deepens the understanding of the geological features of deep shale gas reservoirs but also provides a new perspective for understanding the overpressure mechanisms and reservoir properties of deep shale gas reservoirs. Moreover, it is of significant importance for guiding the exploration and development of deep Longmaxi shale and provides valuable references for further research in related fields.

Mussel-inspired interface deposition strategy for mesoporous metal-phenolic nanospheres with superior antioxidative, photothermal and antibacterial performance

Metal-phenolic networks (MPNs) have emerged as a versatile and multifunctional platform applied in bioimaging, disease treatment, electrocatalysis, and water purification. The synthesis of MPNs with mesoporous frameworks and ultra-small diameters (<200 nm), crucial for post-modification, cargo loading, and mass transport, remains a formidable challenge. Inspired by mussel chemistry, mesoporous metal-phenolic nanospheres (MMPNs) are facilely prepared by direct deposition of the metal-polyphenol complex on the interface of oil nano-droplets composed of block copolymers/1,3,5-trimethylbenzene followed by a spontaneous template-removal process. Due to the penetrable and stable networks, the oil nano-droplets gradually leak from the networks driven by shear stress during the stirring process. As a result, MMPNs are obtained without additional template removal procedures such as solvent extraction or high-temperature calcination. The materials have a large pore size (∼12.1 nm), uniform spherical morphology with a small particle size (∼99 nm), and a large specific surface area (49.8 m2 g−1). Due to the abundant phenolic hydroxyl groups, the MMPNs show excellent antioxidative property. The MMPNs also have excellent photothermal property, whose photothermal conversion efficiency was 40.9 %. Moreover, the phenolic hydroxyl groups can reduce Ag+ in situ to prepare Ag nanoparticles loaded MMPNs composites, which have excellent inhibition performance of drug-resistant bacteria biofilm.

Vat photopolymerization 3D printing of Al2O3 ceramic cores with strip‐shaped pores by using polyamide 6 fiber template

AbstractThe complex ceramic core used for hollow turbine blades requires high porosity and flexural strength. This work combined vat photopolymerization 3D printing with sacrificial template method to prepare Al2O3 ceramic cores with strip‐shaped pores using polyamide 6 (PA6) fibers as templates. When the porosity was greater than 30%, the maximum flexural strength reached up to 110.48 MPa. The sacrificial templating method improved the porosity of Al2O3 ceramic cores, forming an internal porous structure that combined strip‐shaped large pores with irregularly shaped small pores. The influences of PA6 fiber content and diameter on the shrinkage, porosity, microstructure, and comprehensive properties of alumina ceramic cores were studied, revealing the mechanism of the coexistence of high porosity and high strength.

Hierarchical pore structure with a confined resonant mode for improving the solar energy utilizing efficiency of ultra-thin perovskite solar cells

The perovskite solar cell (PSC) has the benefits of flexibility, inexpensiveness, and high efficiency, and has important prospective applications. However, serious optical losing and low solar energy-utilizing efficiency remain a challenge for the ultra-thin PSCs because of the interface reflection of traditional planar structure. In this study, a hierarchical pore structure with a confined resonant mode is introduced and optimized by electromagnetic theory to improve the solar energy absorbing and utilizing efficiency of ultra-thin PSCs. The large pores in the top layer that support a whispering gallery mode can focus and guide the incident light into the solar cell. The small pores in the bottom layer enable backward scattering of the unabsorbed light and can improve the effective absorption of active layer. The finite-difference time-domain method is employed to optimize the geometric parameters of hierarchical pore structure to improve the light absorption of PSCs. The proposed resonant hierarchical pore structure can greatly improve sunlight absorption of ultra-thin PSCs, and the effective light absorption and photocurrent of PSCs with a hierarchical pore structure is 20.7% higher than that of PSCs with traditional planar structure. This work can offer a beneficial guideline for improving solar energy utilizing efficiency of various thin-film solar cells.

Ternary Phase-Field Simulation of Poly(vinylidene fluoride) Microporous Membrane Structures Prepared by Nonsolvent-Induced Phase Separation with Different Additives and Solvent Treatments.

In this study, an existing ternary membrane system based on nonsolvent-induced phase separation (NIPS) with a phase-field model was optimized. To study and analyze the effects of different additives on the formation of the skin layer and the effects of the three solvents on membrane characterization under the same conditions, two-dimensional simulations of the relevant parameters of a poly(vinylidene fluoride) (PVDF) membrane system were performed. The specific application of quaternary substances in ternary membrane systems was elaborated by determining the cohesive energy density between the additives and solvents, followed by the interaction parameters χ under the joint effect of the two. The results showed that the PVDF microporous membrane formed a dense surface layer at the mass transfer exchange interface, and with an increase in the poly(ethylene glycol) (PEG) concentration, the phase separation of the skin layer was predominantly transformed from liquid-solid partitioning to liquid-liquid partitioning; the number of membrane pores increased with increasing poly(vinylpyrrolidone) (PVP) concentration. The N,N-dimethylacetamide (DMAc) solvent system had the most stable thermodynamic properties; the dimethyl sulfoxide (DMSO) solvent system had mostly large pores running through the membrane and exhibited a porous structure. Related experiments also validated the model. Therefore, this model can be applied to other PVDF ternary membrane systems to better understand the structural development of microporous PVDF membranes under different conditions.

High Consistency Silicone Rubber Foams.

Silicone elastomers are high-performance plastics. In the extrusion process, only high-consistency silicone rubbers were used. In order to reduce the cost and weight, silicone rubbers can be foamed during processing. In this study, high-consistency silicone rubber is processed with different physical and chemical blowing agents. The resulting reaction kinetics, as well as the mechanical and morphological properties, had been investigated and compared with each other. This showed that the chemical blowing agent significantly influenced the crosslinking reaction compared to the microspheres and the water/silica mixture tested, but it also achieved the lowest density compared to the physical blowing agents. When evaluating the foam morphology, it became clear that the largest number of pores was achieved with the microspheres and the largest pores when using the water/silica mixture. Furthermore, it has been shown that the different mechanisms of action of the blowing agents have a major influence on the mechanical properties, such as the micro shore hardness and the foam morphology.

Effect of confining pressure on the damage characteristics and mechanism of granite under ultra-high-frequency impact

Assisted ultra-high-frequency impact technology is a promising method for improving hard rock-breaking efficiency in geotechnical and petroleum engineering. However, previous studies did not consider the effects of in situ stress. In this study, triaxial ultra-high-frequency impact tests were conducted at confining pressures ranging from 0 to 20 MPa. Using nuclear magnetic resonance, infrared thermal radiation, crack dye penetrant, and scanning electron microscope tests, the influence of confining pressure on the macro, meso, and micro damage characteristics and mechanism of granite was revealed. The results indicate that with the increasing confining pressure, the porosity increment of small pores continuously decreases from 0.2% to −0.02%; the moderate pores first increase to a peak of around 0.18% before 6 MPa and then gradually decrease to around zero. The large pores began to increase after 8 MPa, increasing to around 0.05% when the confining pressure was 14 MPa. In addition, the failure mode first changed from tensile splitting damage to a relatively intact state with meso-damage, and finally, transverse shear fracture occurred owing to the higher shear stress and low mode II fracture toughness near the crack tips. These findings prove the effectiveness of ultra-high-frequency impact technology in weakening hard rock in deep strata.

A novel strategy for preparing high-performance, low-cost biomass charcoal for dye adsorption using aquatic agricultural waste lotus stem fibers

In this study, lotus stem (LS), a natural, abundant, and underutilized aquatic agricultural waste, was used to prepare biochar (BC) as a potential adsorbent for sewage treatment. A two-step process for the production of LS based nitrogen-doped BC (NLBC) has been developed, involving low-temperature pyrolysis of LS and urea mixture, followed by high-temperature pyrolysis of the pre-carbonized BC via NaOH immersion technique. The two-step activation treatment not only can effectively maintain the structural integrity of LS, but contribute to exposing more active sites for effective adsorption of methylene blue (MB). The obtained NLBC possesses a large pore volume (0.997 cm3 g−1) and great specific surface area of 1478.93 m2 g−1, contributing to its maximum adsorption capacity of 2320.81 mg g−1 for MB. The behavior of MB adsorbed onto NLBC conforms to pseudo-second-order kinetics and Langmuir–Freundlich models. The adsorption capacity remains stable across a range of pH, varying salt concentrations, and cyclic repetitions. The adsorption mechanism was ascribed to the synergetic effects of pore filling, H-bonding, and electrostatic interaction through comparative analysis before and after adsorption. The results indicate that NLBC is an environmentally friendly, cost-effective, and efficient for dye-containing wastewater treatment.

High Hydrogen Storage in Trigonal Prismatic Monomer-based Highly Porous Aromatic Frameworks.

Hydrogen storage is crucial in the shift toward a carbon-neutral society, where hydrogen serves as a pivotal renewable energy source. Utilizing porous materials can provide an efficient hydrogen storage solution, reducing tank pressures to manageable levels and circumventing the energy-intensive and costly current technological infrastructure. Herein, we report two highly porous aromatic frameworks (PAFs), C-PAF and Si-PAF, prepared through a Yamamoto C-C coupling reaction between trigonal prismatic monomers. These PAFs exhibited large pore volumes and BET areas, 3.93 cm3 g-1 and 4857 m2 g-1 for C-PAF, and 3.80 cm3 g-1 and 6099 m2 g-1 for Si-PAF, respectively. Si-PAF exhibited a record-high gravimetric hydrogen delivery capacity of 17.01 wt% and a superior volumetric capacity of 46.5g L-1 under pressure-temperature swing adsorption conditions (77 K, 100bar → 160 K, 5bar), outperforming benchmark hydrogens storage materials. By virtue of the robust C-C covalent bond, both PAFs showed impressive structural stabilities in harsh environments and unprecedented long-term durability. Computational modeling methods were employed to simulate and investigate the structural and adsorption properties of the PAFs. These results demonstrate that C-PAF and Si-PAF are promising materials for efficient hydrogen storage. This article is protected by copyright. All rights reserved.

Dehydration-Induced Cluster Consolidation in a Metal-Organic Framework for Sieving Hexane Isomers.

Metal-organic frameworks (MOFs) that exhibit dynamic phase-transition behavior under external stimuli could have great potential in adsorptive separations. Here we report on a zinc-based microporous MOF (JNU-80) and its reversible transformation between two crystalline phases: large pore (JNU-80-LP) and narrow pore (JNU-80-NP). Specifically, JNU-80-LP can undergo a dehydration-induced cluster consolidation under heat treatment, resulting in JNU-80-NP with a reduced channel that allows exclusion of di-branched hexane isomers while high adsorption of linear and mono-branched hexane isomers. We further demonstrate the fabrication of MOF-polymer composite (JNU-80-NP-block) and its application in the purification of di-branched isomers from liquid-phase hexane mixtures (98% di-branched) at room temperature, affording the di-branched hexane isomers with 99.5% purity and close to 90% recovery rate over ten cycles. This work illustrates an interesting dehydration-induced cluster consolidation in MOF structure and the ensuing channel shrinkage for sieving di-branched hexane isomers, which may have important implications for the development of MOFs with dynamic behavior and their potential applications in non-thermal driven separation technologies.

Numerical Study on Permeability of Reconstructed Porous Concrete Based on Lattice Boltzmann Method

The reconstruction of the porous media model is crucial for researching the mesoscopic seepage characteristics of porous concrete. Based on a self-compiled MATLAB program, a porous concrete model was modeled by controlling four parameters (distribution probability, growth probability, probability density, and porosity) with clear physical meanings using a quartet structure generation set (QSGS) along with the lattice Boltzmann method (LBM) to investigate permeability. The rationality of the numerical model was verified through Poiseuille flow theory. The results showed that the QSGS model exhibited varied pore shapes and disordered distributions, resembling real porous concrete. Seepage velocity distribution showed higher values in larger pores, with flow rates reaching up to 0.012 lattice point velocity. The permeability–porosity relationship demonstrated high linearity (the Pearson correlation coefficient is 0.92), consistent with real porous concrete behavior. The integration of QSGS-LBM represents a novel approach, and the research results can provide new ideas and new means for subsequent research on the permeability of porous concrete or similar porous medium materials.

Effect of magnetic field coupled magnetic biochar on membrane bioreactor efficiency, membrane fouling mitigation and microbial communities

The excitation by magnetic field was established to mitigate the membrane fouling of magnetic biochar (MB)-supplemented membrane bioreactor (MBR) in this study. The results showed that the transmembrane pressure (TMP) increase rates decreased by about 8 % after introducing the magnetic field compared with the magnetic biochar-MBR (MB-MBR). Membrane characterization suggested that the flocs in the magnetic field-magnetic biochar-MBR (MF-MB-MBR) formed a highly permeable developed cake layer, and a fluffier and more porous deposited layer on membrane surface, which minimized fouling clogging of the membrane pores. Further mechanistic investigation revealed that the decrease in contact angle of fouled membrane surface in MF-MB-MBR, i.e. an enhanced membrane hydrophilicity, is considered important for forming highly permeable layers. Additionally, the magnetic field was demonstrated to have a positive effect on the improvement of the magneto-biological effect, the enhancement of charge neutralization and adsorption bridging between sludge and magnetic biochar, and the reduction of formation of extracellular polymeric substances (EPSs), which all yielded sludge flocs with a large pore structure conducive to form a fluffy and porous deposited layer in the membrane surface. Furthermore, high-throughput sequencing analysis revealed that the magnetic field also led to a reduction in microbial diversity, and that it promoted the enrichment of specific functional microbial communities (e.g. Bacteroidetes and Firmicutes) playing an important role in mitigating membrane fouling. Taken together, this study of magnetic field-enhanced magnetic biochar for MBR membrane fouling mitigation provides insights important new ideas for more effective and sustainable operation strategies.

Wireless Gas Sensor Based on the Mesoporous ZnO-SnO2 Heterostructure Enables Ultrasensitive and Rapid Detection of 3-Methylbutyraldehyde.

Achieving ultrasensitive and rapid detection of 3-methylbutyraldehyde is crucial for monitoring chemical intermediate leakage in pharmaceutical and chemical industries as well as diagnosing ventilator-associated pneumonia by monitoring exhaled gas. However, developing a sensitive and rapid method for detecting 3-methylbutyraldehyde poses challenges. Herein, a wireless chemiresistive gas sensor based on a mesoporous ZnO-SnO2 heterostructure is fabricated to enable the ultrasensitive and rapid detection of 3-methylbutyraldehyde for the first time. The mesoporous ZnO-SnO2 heterostructure exhibits a uniform spherical shape (∼79 nm in diameter), a high specific surface area (54.8 m2 g-1), a small crystal size (∼4 nm), and a large pore size (6.7 nm). The gas sensor demonstrates high response (18.98@20 ppm), short response/recovery times (13/13 s), and a low detection limit (0.48 ppm) toward 3-methylbutyraldehyde. Furthermore, a real-time monitoring system is developed utilizing microelectromechanical systems gas sensors. The modification of amorphous ZnO on the mesoporous SnO2 pore wall can effectively increase the chemisorbed oxygen content and the thickness of the electron depletion layer at the gas-solid interface, which facilitates the interface redox reaction and enhances the sensing performance. This work presents an initial example of semiconductor metal oxide gas sensors for efficient detection of 3-methylbutyraldehyde that holds great potential for ensuring safety during chemical production and disease diagnosis.

Investigation into the strength and toughness of polyvinyl alcohol fiber-reinforced fly ash-based geopolymer composites

This study investigates the influence of polyvinyl alcohol (PVA) fiber dosage and length on the porosity, mechanical strength, and toughness of fly ash-based geopolymer composites. The experimental data are analyzed to examine the deflection-load relationship in the flexural toughness tests of fiber-reinforced geopolymer composites (FRGPC) with different PVA fiber parameters. The results indicate that the addition of a certain amount of PVA fibers effectively enhances the flexural resistance of FRGPC. Particularly, the optimal performance is achieved with the addition of 2.0 vol% of 9 mm PVA fibers, where the 28-day flexural strength reaches 13.16 MPa, representing a 150.95 % increase compared to the control group, and the deflection at peak load increases by 308.00 %. However, the compressive strength of FRGPC with PVA fiber dosage at 1.6 vol%, 2.0 vol%, and 2.4 vol% decreases by 0.89 %, 6.39 %, and 10.13 %, respectively. Microscopic observations of FRGPC indicate that an increase in fiber dosage and length results in larger pores and uneven distribution of fibers. Notably, 12 mm PVA fibers exhibit significant aggregation, confirming the findings from mechanical property tests. This study, through an in-depth exploration of the mechanical properties of PVA fiber-reinforced fly ash-based geopolymer composites, provides crucial experimental data and a theoretical foundation for the development of sustainable construction materials.