Microporous Structure Research Articles

Simulation and Optimization of Transmitting Transducers for Well Logging.

Piezoelectric transducers are commonly used in acoustic well logging. However, the low frequency and narrow range of the acoustic waves limit the achievable detection accuracy. In addition, the low amplitude of the waves causes useful information to be easily masked by noise during detection, which affects the accuracy of geological identification and makes it difficult to detect formations tens of meters away. This paper proposes a microporous liquid-electric transmission transducer, in which the microporous electrode structure generates a powerful shock wave through a high-energy instantaneous discharge. First, a model of the liquid-electric microporous transmitting transducer was constructed by combining simulations with numerical calculations, and its electro-acoustic characteristics were analyzed. Then, based on the survey requirements, two innovative optimization schemes for the microporous electrode structure were proposed, namely a triangular pyramid microporous electrode structure and a rectangular microporous electrode structure, and their performances were compared. The results show that the newly optimized triangular pyramid microporous electrode liquid-electric transducer generates acoustic waves with higher amplitude and a wider frequency range than conventional piezoelectric transducers and other microporous structures. It maintains high energy while achieving high frequencies, enabling detection at distances of up to hundreds of meters and the precise characterization of small geological bodies. This has significant implications for applications in marine exploration, land exploration, clean energy, and new energy fields.

The Effect of a HealiAid ® Collagen Wound Dressing on Wound Healing in Patients: A Randomized Double-Blind Pilot Clinical Trial

Wound healing is a complex, multi-phase process. With rising healthcare costs, an aging population, and increasing chronic disease prevalence, the burden of wound care is escalating. Thus, finding safe and effective methods to accelerate wound healing is crucial. This study aims to explore the safety and efficacy of HealiAid® Collagen Wound Dressing in treating various types of wounds, including venous ulcers, diabetic foot ulcers, pressure ulcers, and burns. A clinical trial was conducted on 18 subjects with venous ulcers, diabetic foot wounds, pressure ulcers, and burn wounds. The study assessed the effectiveness of HealiAid in different wound types by analyzing its thermal stability, porous structure, biocompatibility, and clinical efficacy. Wound healing was strictly monitored, and the safety and tolerability of the dressing were evaluated. The results showed that HealiAid Collagen Wound Dressing has excellent thermal stability and structural integrity. Its porous microstructure enhances cell adhesion and tissue regeneration, demonstrating significant healing effects across various wound types, including venous ulcers, diabetic foot wounds, pressure ulcers, and burns. No serious adverse reactions were reported, and endotoxin levels were well below safety standards. This study confirms the safety and efficacy of HealiAid Collagen Wound Dressing in treating multiple wound types. Its outstanding thermal stability, porous structure, and biocompatibility make it a promising option for clinical wound care

Enhancement of critical current density using micro-porous structure in a low-temperature water electrolysis

The critical current density (CCD), which limits the hydrogen production rate was measured by forming micro-porous structures on the cathode electrode in a low-temperature water electrolysis. Several micro-porous structures were formed by the electrodeposition method varying the current density during the deposition. A maximum 54% enhancement of the CCD was recorded compared to the plain surface. With the micro-porous structures, the superior capillary wicking effect allowed the electrolyte to penetrate the structure, resulting in the increased number of hydrogen nucleation sites. The increased hydrogen nucleation sites led to the decreased hydrogen bubble size and increased departed bubble density, which delayed formation of the hydrogen film leading to the CCD. The surface morphology revealed that the multiple pore layers with the interconnected pores exhibited superior capillary wicking effect compared to the open type single pore layer. It is expected that the results of present work stimulate further research regarding electrode surface design in the low-temperature water electrolysis.

High-fidelity reconstruction of porous cathode microstructures from FIB-SEM data with deep learning

Accurate modeling of lithium-ion battery (LIB) electrode microstructures provides essential references for understanding degradation mechanisms and optimizing materials. Traditional segmentation methods often struggle to accurately capture the complex microstructures of porous LIB electrodes in focused ion beam scanning electron microscopy (FIB-SEM) data. In this work, we develop a deep learning model based on the Swin Transformer to segment FIB-SEM data of a lithium cobalt oxide electrode, utilizing fused secondary and backscattered electron images. The proposed approach outperforms other deep learning methods, enabling the acquirement of 3D microstructure with reduced particle elongated artifacts. Analyses of the segmented microstructures reveal improved electrode tortuosity and pore connectivity crucial for ion and electron transport, emphasizing the necessity of accurate 3D modeling for reliable battery performance predictions. These results suggest a path toward voxel-level degradation analysis through more sensible battery simulation on high-fidelity microstructure models directly twinned from real porous electrodes.

Soft Matter Electrolytes: Mechanism of Ionic Conduction Compared to Liquid or Solid Electrolytes

Soft matter electrolytes could solve the safety problem of widely used liquid electrolytes in Li-ion batteries which are burnable upon heating. Simultaneously, they could solve the problem of poor contact between electrodes and solid electrolytes. However, the ionic conductivity of soft matter electrolytes is relatively low when mechanical properties are relatively good. In the present review, mechanisms of ionic conduction in soft matter electrolytes are discussed in order to achieve higher ionic conductivity with sufficient mechanical properties where soft matter electrolytes are defined as polymer electrolytes and polymeric or inorganic gel electrolytes. They could also be defined by Young’s modulus from about Pa to Pa. Many soft matter electrolytes exhibit VFT (Vogel–Fulcher–Tammann) type temperature dependence of ionic conductivity. VFT behavior is explained by the free volume model or the configurational entropy model, which is discussed in detail. Mostly, the amorphous phase of polymer is a better ionic conductor compared to the crystalline phase. There are, however, some experimental and theoretical reports that the crystalline phase is a better ionic conductor. Some methods to increase the ionic conductivity of polymer electrolytes are discussed, such as cavitation under tensile deformation and the microporous structure of polymer electrolytes, which could be explained by the conduction mechanism of soft matter electrolytes.

Aminated ZIF‐8 to facilitate CO2 sieving through polyvinyl alcohol/ionic liquid membranes

AbstractCO2 separation technology at low pressure is most desirable in carbon capture projects to mitigate global warming. Facilitated transport membranes offer selective and effective CO2 permeation using a wide range of carbon carriers at low pressure. Porous fillers were recently included as they can carry abundant fixed carriers besides offering open channels for CO2 permeation. This study investigates the effects of amine‐modified zeolitic imidazolate framework‐8 (ZIF‐8) with well‐defined micropores and gas sieving ability in polyvinyl alcohol (PVA) membranes containing an ionic liquid that worked as mobile carriers. The effects of amine‐modified ZIF‐8 and silica nanoparticles on membrane properties and separation performance were also compared. Fourier transform infrared spectra confirmed the incorporation of ZIF‐8, secondary amine, IL anions, and silica nanoparticles in PVA membranes. Energy dispersive analysis showed the good dispersion of inorganic fillers. The amine‐modified silica nanoparticles resulted in higher thermal stability compared to the amine‐modified ZIF‐8 in PVA membranes containing [bmin][Ac] ionic liquid, as shown in the thermogravimetric analysis. However, the CO2 separation performance of PVA membranes containing [bmim][Ac] ionic liquid was improved more significantly by the amine‐modified ZIF‐8 with microporous structure. A CO2/N2 ideal selectivity of 85.65 and CO2 permeance up to 4,502.91 GPU were attained. Unlike the CO2/N2 ideal selectivity, the CO2 permeance was not significantly affected either using [bmin][Ac] or [bmin][BF4]. The humid gas greatly enhanced the CO2 permeance without much changes in the CO2/N2 ideal selectivity due to the promotion of facilitated transport. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.

Insights into the pore structure effect on the mass transfer of fuel cell catalyst layer via combining machine learning and multiphysics simulation

Analysis of the catalytic layer (CL) pore structure and three-phase (electron phase, proton phase, and reactant phase) mass transfer in high-temperature polymer electrolyte membrane fuel cell (HT-PEMFC) is critical for improving concentration polarization and optimizing performance. However, there is a lack of studies on the pore structure’s impact on the catalytic layer three-phase mass transfer. In this work, the influence of pore structure on catalytic layer three-phase mass transfer and multiphysics distribution was investigated by combining machine learning and multiphysics simulation. Among many key factors investigated by machine learning that impact the performance of catalytic layer, porosity emerges as the primary influencing factor. Porosity accounts for 32.7 % of the electric potential drop, with macro/micro porosity contributing 27.6 % and 5.1 %, and 32.8 % of the current density, with macro/micro porosity contributing 15.6 % and 17.2 %. Furthermore, the macropore structure has a much greater influence on the performance of the catalytic layer compared to the micropore structure. Moreover, the simulation results demonstrated that porosity has a great influence on three-phase mass transfer, the oxygen molarity increases with increasing porosity. The electric potential difference increases exponentially as porosity increases. The relationship between current density and porosity is a volcanic relationship, which can be expressed as a quadratic polynomial function. The mesoscopic pore-scale model (PSM) with an εeff of 0.502 (εmic of 0.2 and εmac of 0.378) exhibits the highest mean current density at 619.526 mA/cm2@0.5 V, attributed to a more uniform and efficient three-phase transfer path. The accuracy of the mesoscopic pore-scale model and the polynomial equation is further confirmed through corresponding experiments. The experiment results show that the current density decreased as the εeff increased from 0.682 to 0.702, which aligns with the theoretical predictions of the PSM model and polynomial equation. These studies are valuable for comprehending the internal three-phase mass transfer behavior and optimizing the catalytic layer pore structure to enhance HT-PEMFC performance.

Recent Advances in MXene-Based Aerogels for Electromagnetic Wave Absorption.

Developing lightweight, high-performance electromagnetic wave (EMW) absorbing materials those can absorb the adverse electromagnetic radiation or waves are of great significance. Transition metal carbides and/or nitrides (MXenes) are a novel type of 2D nanosheets associated with a large aspect ratio, abundant polar functional groups, adjustable conductivity, and remarkable mechanical properties. This contributes to the high-efficiency assembly of MXene-based aerogels possessing the ultra-low density, large specific surface area, tunable conductivity, and unique 3D porous microstructure, which is beneficial for promoting the EMW absorption. Therefore, MXene-based aerogels for EMW absorption have attracted widespread attention. This review provides an overview of the research progress on MXene-based aerogels for EMW absorption, focusing on the recent advances in component and structure design strategies, and summarizes the main strategies for constructing EMW absorbing MXene-based aerogels. In addition, based on EMW absorption mechanisms and structure regulation strategies, the preparation methods and properties of MXene-based aerogels with varieties of components and pore structures are detailed to advance understanding the relationships of composition-structure-performance. Furthermore, the future development and challenges faced by MXene-based aerogels for EMW absorption are summarized and prospected.

ON-OFF Switching of Photocatalytic Hydrogen Evolution by Built-in Pt-Nitrogen-Carbon Reticular Heterojunctions.

COF engineering with a built-in, high concentration of defined N-doped sites overcomes the "black-box" drawback of conventional trial-and-error N-doping methods (used in polymeric carbon nitride and graphene), that hamper a directed evolution of functional carbon interfaces based on structure-reactivity guidelines. The cutting-edge challenge is to dissect the many complex and interdependent functions that originate from reticular N-doping, including modification of the material optoelectronics, band alignments, interfacial contacts and co-localization of active-sites, producing a multiple-set of effectors that can all play a role to regulate photocatalysis. Herein, an ON-OFF gated photocatalytic H2 evolution (PHE) is dictated by the Pt-NPyridine-carbon active sites and probed with a dual COF platform, based on stable β-ketoenamine connectivities made of triformylphloroglucinol (Tp) as the acceptor knots and 1,4-diaminonaphtalene (Naph) or 5,8-diaminoisoquinoline (IsoQ) as donors. Our results showcase two novel COF-Naph-Tp and COF-IsoQ-Tp frameworks featuring quasi-identical slip-stacked microporous structure, and similar surface area, band gap, light harvesting envelope up to 700 nm, fluorescence emission profile/lifetime, and PEIS response at the surface/water interface (Rct=16-10±4 KΩ). A divergent behaviour is indeed observed for COF-IsoQ-Tp with record photoelectrochemical outputs (J=-16 μA cm-2, Rt=3 KΩ at 0.40 V vs RHE) and two orders of magnitude higher rate of PHE (11.3 mmol g-1 h-1, λ>400 nm, pH 5) compared to the inactive COF-Naph-Tp analogue. It turns out that PHE is regulated by the isoquinoline residues at the COF pores where emergent Pt-NPyridine-carbon functional heterojunctions are formed upon photo-deposition of Pt nanoparticles as co-catalysts, as probed by combined XPS and DFT calculations evidence. This work sets a key guideline to direct the design of carbon-based materials encoding the installation of metal-nitrogen-carbon active sites within tailored coordination environments enabling the catalytic performance.

Porous and Conductive Fiber Woven Textile for Multi‐Functional Protection, Personal Warmth, and Intelligent Motion/Temperature Perception

AbstractIndustrialization and human activities have introduced numerous hazards, including exposure to harsh chemicals, radiation, static electricity, and fire risks, particularly in high‐risk sectors such as engineering, rescue operations, military, and aerospace. This study presents a multi‐functional protective textile developed from a conductive fiber composed of polytetrafluoroethylene (PTFE) and carbon nanotubes (CNT), crucial for ensuring personal safety. The conductive fiber demonstrates remarkable strength (17.3 MPa), high porosity (76%), and significant electrical conductivity (185 S m−1), coupled with excellent fineness and flexibility due to its dual‐nanofibrous structure. The resulting textile exhibits exceptional hydrophobicity, chemical resistance, and high electromagnetic interference shielding effectiveness (29 dB in the X‐band), alongside a superior UV protective factor (>3000) and anti‐static properties. Notably, it possesses outstanding electro/photo thermal conversion capabilities, enabling consistent heat generation for personal warmth. Additionally, the textile responds electrically to deformation and temperature changes, facilitating intelligent applications such as motion and temperature monitoring and fire alerts. This work offers a novel strategy for fabricating PTFE‐based composite fibers with porous microstructures and high electrical conductivity, setting a new standard for next‐generation protective clothing with advanced functionalities.

Catalytic and Electrochemical Study of Cu-ZSM-5/MCM-41.

Hierarchically structured micro-mesoporous ZSM-5/MCM-41 composite materials incorporating copper ions were synthesized using pre-synthesized ZSM-5 and cetyltrimethylammonium bromide (CTAB) as a template for forming the MCM-41 structure. The composites were characterized through powder X-ray diffraction, N2 adsorption-desorption, diffuse reflectance spectroscopy (UV-vis DRS), Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and energy dispersive X-ray spectroscopy. X-ray diffraction confirmed well-ordered ZSM-5 and MCM-41 structures, and UV-vis DRS showed successful copper ion incorporation. N2 adsorption-desorption revealed the presence of both microporous and mesoporous structures. To evaluate their catalytic performance, Cu-incorporated ZSM-5/MCM-41 composite catalysts were assessed through the oxidation reaction of ethylbenzene using tert-butyl hydroperoxide (TBHP) as the oxidizing agent. With a 9% (w/w) Cu-ZM-5 (5 wt % copper-incorporated ZSM-5/MCM-41) catalyst and an oxidant to ethylbenzene molar ratio of 2:1 at 40 °C in the absence of a solvent for 4 h, the process yielded acetophenone (93.2%) as the major product. Additionally, these Cu-incorporated composites were examined as electrode materials for electrochemical storage. Cyclic voltammetry and galvanostatic charge-discharge studies showed that Cu-ZM-5 exhibited pseudocapacitive behavior, with a capacitance of up to 366 F g-1 at a current density of 1 A g-1, surpassing ZSM-5 and ZSM-5/MCM-41. These results highlight Cu-ZM-5's potential as an effective electrode material for electrochemical storage applications like supercapacitors.

Bioinspired Glycopeptide Hydrogel Reestablishing Bone Homeostasis through Mediating Osteoclasts and Osteogenesis in Periodontitis Treatment.

Irreversible alveolar bone resorption is one of the important clinical manifestations of periodontitis, which is initiated by a plaque biofilm and exacerbated by the imbalance of osteoclast activity and osteogenesis, affecting a patient's masticatory function and resulting in a high recurrence rate of periodontitis. Herein, to reestablish bone homeostasis in periodontitis, a minocycline hydrochloride (MH)-loaded glycopeptide hydrogel (MH/GRWgel) is fabricated to mediate alveolar bone absorption through sequential antibacterial and RANKL-blocking activities. GRWgel shows an ECM-like fibrous and porous microstructure serving as a scaffold for cell proliferation and differentiation and holds the merits including injectability, self-healing properties, and good biocompatibility. After injection in situ, MH is released rapidly from the hydrogel in the early stage, demonstrating a potent antimicrobial effect to combat the biofilm in the deep periodontal pocket. Moreover, MH/GRWgel exhibits a high specific binding efficiency with RANKL to suppress osteoclast maturation by shielding the RANKL/RANK interaction and enhancing osteogenic differentiation, thereby synergistically regulating bone homeostasis. In the rat periodontitis model, MH/GRWgel significantly curtails periodontitis progression through antimicrobial activity, inhibition of alveolar bone resorption, and promotion of bone regeneration, which is superior to the treatment of a commercial gel. These findings suggest that MH/GRWgel with superiority in regulating bone homeostasis provides a promising therapeutic strategy for periodontitis.

Advancing self‐lubricating technology: Selective laser sintering molding assisted development of copper‐based polytetrafluoroethylene /graphite composites

AbstractThis study introduces an innovative technique for the fabrication of copper‐based polytetrafluoroethylene (PTFE)/graphite self‐lubricating composites. By harnessing the exceptional capabilities of selective laser sintering (SLS), we efficiently create three‐dimensional, continuous, and porous graphite preforms. Following this, the composite is formed through a combination of electroplating and vacuum extrusion methods. Subsequently, PTFE was vacuum impregnated into the microporous structure of the graphite preforms, and the composites were obtained through freeze‐drying, plasticizing, and machining processes. The resulting copper‐based PTFE/graphite self‐lubricating composites exhibit an exceptional blend of properties. Notably, there is a significant reduction in the average coefficient of friction, dropping from 0.14 to 0.02, and a marked decrease in the wear rate, from 1.358 × 10−5 to 1.109 × 10−5 mm3/N·m, as compared to graphite as a standalone lubricant. This represents a substantial improvement in performance, underscoring the effectiveness of the proposed fabrication method.Highlights The porous graphite with controllable shape distribution was prepared. Surface copper plating improves surface bonding. Controllable copper matrix composites with double lubricant were prepared. The average friction coefficient is as low as 0.02.

Single-Crystalline 3D Covalent Organic Frameworks with Exceptionally High Specific Surface Areas and Gas Storage Capacities.

Single-crystalline covalent organic frameworks (COFs) are highly desirable toward understanding their pore chemistry and functions. Herein, two 50-100 μm single-crystalline three-dimensional (3D) COFs, TAM-TFPB-COF and TAPB-TFS-COF, were prepared from the condensation of 4,4',4″,4‴-methanetetrayltetraaniline (TAM) with 3,3',5,5'-tetrakis(4-formylphenyl)bimesityl (TFPB) and 3,3',5,5'-tetrakis(4-aminophenyl)bimesityl (TAPB) with 4,4',4″,4‴-silanetetrayltetrabenzaldehyde (TFS), respectively, in 1,4-dioxane under the catalysis of acetic acid. Single-crystal 3D electron diffraction reveals the triply interpenetrated dia-b networks of TAM-TFPB-COF with atom resolution, while the isostructure of TAPB-TFS-COF was disclosed by synchrotron single-crystal X-ray diffraction and synchrotron powder X-ray diffraction with Le Bail refinements. The nitrogen sorption measurements at 77 K disclose the microporosity nature of both activated COFs with their exceptionally high Brunauer-Emmett-Teller surface areas of 3533 and 4107 m2 g-1, representing the thus far record high specific surface area among imine-bonded COFs. This enables the activated COFs to exhibit also the record high methane uptake capacities up to 28.9 wt % (570 cm3 g-1) at 25 °C and 200 bar among all COFs reported thus far. This work not only presents the structures of two single-crystalline COFs with exceptional microporosity but also provides an example of atom engineering to adjust permanent microporous structures for methane storage.

The influence of pore throat heterogeneity and fractal characteristics on reservoir quality: A case study of chang 8 member tight sandstones, Ordos Basin

The Chang 8 member of the Yanchang Formation in the Ordos Basin exhibits extensive development of tight sandstone reservoirs. In comparison to conventional reservoirs, these tight sandstone reservoirs demonstrate smaller pore-throat systems and stronger heterogeneity due to interactions between inherent sedimentary components and various diagenetic processes. To further investigate the influence of microscopic pore throat structure on macroscopic physical properties and oil content within the reservoir, a comprehensive study was conducted utilizing high pressure mercury injection, nuclear magnetic resonance, X-CT scanning, and other pore throat testing methods. This study was complemented by observation techniques such as polarizing microscope, scanning electron microscopy, and laser confocal imaging, to study the pore throat system of reservoirs under the influence of different sedimentary components and diagenesis. By comparison, it is observed that the radius of the primary pore throat system in the tight sandstone reservoir ranges from 0.01 to 1 μm. The structural characteristics of the pore throat system significantly impact the macroscopic physical properties of the reservoir. Due to variations in testing methods, high pressure mercury injection, nuclear magnetic resonance (NMR), and X-ray computed tomography (X-CT) reveal different fractal dimensions of the reservoir's pore throat system. Therefore, it is better to respectively utilize fractal dimension Df2, Df2-NMR, Df2-CT, and pore throat parameters to characterize the microscopic pore throat system with a radius ranging from 0.01 to 1 μm. The decrease in the average pore throat radius and the increased irregularity of pore shape contribute to heightened heterogeneity in the micro-pore throat structure within the reservoir. This negatively impacts its physical properties and oil content. Furthermore, it is important to note that the minimum threshold of pore throat radius plays a crucial role as a primary factor determining the fluid seepage capacity within this reservoir. Moreover, when isolated pores exist, reduced fluid mobility ensues, which further worsens the seepage conditions of the reservoir. The chlorite rims development reservoir shows a low fractal dimension in its micro-pore throats, contributing to superior macroscopic petrophysical properties and oil content. However, compression, siliceous cementation, and calcite cementation negatively impact the average pore throat radius by increasing micropores, inaccessible pores, and narrow throat content. This results in a stronger heterogeneity of the pore throat structure, leading to poor seepage conditions and lower oil content.

Unravelling the effects of drying techniques on Porphyra yezoensis: Morphology, rehydration properties, metabolomic profile, and taste formation

This study explored the impact of sun drying (SD), freeze drying (FD), oven drying (OD), and microwave drying (MD) on the morphology, rehydration properties, metabolomic profile, and taste formation of Porphyra yezoensis. FD elicited a brighter colour, smooth surface, porous microstructure, and strong rehydration properties in P. yezoensis, while dramatically maintaining the umami, sweetness, and saltiness. OD and MD decreased structural openness owing to tissue collapse and affected water absorption. Metabolomic analysis revealed 1030 metabolites, among which taste-related compounds, especially free amino acids, nucleotides, organic acids, and their derivatives, were the main biomarkers for distinguishing the different drying methods. Their related metabolic pathways, such as taurine and hypotaurine metabolism; purine metabolism; glyoxylate and dicarboxylate metabolism; and citrate cycle, were the most active. A metabolic pathway network of the main taste compounds was built to provide novel insights into the mechanisms underlying the taste profile changes associated with different drying methods.

Enhanced hydrogen storage via microporous defects and Cu(I) sites in HKUST-1

A series of microporous defective HKUST-1 materials (DMT-HK-nF) are synthesized employing varying amounts (n = 10, 30, and 50 wt%) of 3,5-dinitrobenzoic acid (DNBA) and 1,3,5-benzene tricarboxylic acid as linkers. Subsequently, stepwise washing and solvent exchanges are conducted to enhance the density of Cu(I) sites and increases the surface area. DMT-HK-30F exhibits superior H2 storage capacity (2.55 wt% at 77 K, 100 kPa and 0.93 wt% at 298 K, 7 MPa), approximately 41% and 48% higher compared to pristine HKUST-1 (1.82 wt% at 77 K, 100 kPa, and 0.63 wt% at 298 K, 7 MPa), respectively. This improvement is attributed to an increase in Cu(I) sites and the introduction of linker defects. However, further addition of DNBA decreases the H2 storage capacity due to a reduction in Cu(I) sites and surface area caused by the formation of “missing metal cluster” defects. This study demonstrates that the simultaneous introduction of appropriate defects and high-density Cu(I) sites into the microporous structure is an effective strategy for enhancing the hydrogen storage performance of metal-organic frameworks.

New insights into the effects of silicate modulus, alkali content and modification on multi-properties of recycled brick powder-based geopolymer

Utilizing recycled brick powder (RBP) as a green precursor to prepare alkali-activated RBP-based geopolymer (AABG) not only broadens the existing system of alkali-activated materials but also achieves the high-value and low-carbon utilization of clay brick waste. This paper aims to systematically investigate the influence of silicate modulus and alkali content of the alkali-activator on the multi-properties of AABG, while proposing multi-path modification methods to optimize AABG performance. Substituting an appropriate amount of metakaolin with RBP contributes to optimizing the performance of metakaolin-based geopolymers. However, the micro-macro properties of AABG are significantly inferior to those of metakaolin-based geopolymer. Under the same silicate modulus, the micro-macro properties of AABG first improve and then deteriorate with the increase in alkali content. With the alkali content of 8 %, the AABG owns the best microstructure and macro properties. When the alkali content remains constant, an appropriate increase in the silicate modulus of alkali-activator contributes to the performance enhancement of AABG mortar. The average pore diameter of AABG-1.2M-8%, AABG-1.4M-8%, and AABG-1.4M-4% paste is 69.4 nm, 61.8 nm and 111.9 nm. Overall, the AABG with 1.6M silicate modulus and 8 % alkali content shows good performance. For the multi-path modification methods of AABG, decreasing the w/b ratio of AABG can enhance its compressive strength and permeability resistance. Besides, increasing the curing temperature of AABG can optimize its micro-pore structure and macro-properties, achieving optimal performance at a curing temperature of 80 °C. Finally, mixing Ca(OH)2 into AABG promotes the formation of more C-A-S-H, thereby further enhancing the AABG performance. Optimizing the silicate modulus, alkaline content and modification methods, it is feasible to produce AABG with superior micro-macro properties.

Defect-Engineered MOF-801/Sodium Alginate Aerogel Beads for Boosting Adsorption of Pb(II).

Metal-organic frameworks (MOFs) are attractive adsorbents for heavy metal capture due to their superior stability, easy modification, and adjustable pore size. However, their inherent microporous structure poses challenges in achieving a higher adsorption capacity. Defect engineering is considered a simple method to create hierarchical MOFs with larger pores. Here, we employed l-aspartic acid as a mixed linker to bind Zr4+ clusters in competition with fumaric acid of MOF-801 to create defects, and the pore size was increased from 4.66 to 15.65 nm. Mercaptosuccinic acid was subsequently used as a postexchange ligand to graft the resultant MOF-801 by acid-ammonia condensation to further expand the pore size to 22.73 nm. Notably, the -NH2, -COOH, and -SH groups contributed by these two ligands increased the adsorption sites for Pb(II). The obtained defective MOF-801 with larger pores was thereafter loaded onto sodium alginate to form aerogel beads as adsorbents, and an adsorption capacity of 375.48 mg/g for Pb(II) was achieved, which is ∼51 times that of pristine MOF-801. The aerogel beads also exhibited outstanding reusability with a removal efficiency of ∼90.23% after 5 cycles of use. The adsorption mechanism of Pb(II) included ion-exchange interaction, as well as chelation interactions of Pb-O, Pb-NH2, and Pb-S. The versatile combination of defect engineering and composite beads provides novel inspirations for MOF modification for boosting heavy metal adsorption.

MoO3 and AlF3 effect on the properties of porous mullite ceramics with needle‐like microstructure

AbstractPorous mullite ceramics were synthesized via ceramic processing using a local industrial kaolin, alumina, and with AlF3 and MoO3 precursor additives to catalyze the formation of pores and acicular mullite grains. The textural properties, crystalline phases, microstructures, and mechanical properties of the obtained samples were comprehensively analyzed and compared with a reference mullite formulated without additives. The obtained ceramics have a well‐defined porous microstructure, with a porosity of about 50%, and a pore size distribution in the 0.1–2 µm range. Ceramics that involve the addition of MoO3 present well‐defined acicular mullite grains, with slightly higher porosity, larger pores, and better mechanical resistance compared to those processed using AlF3.To correlate the ceramic porosity with its mechanical properties, a simple model of spherical pores was proposed to assess the flexural strength of the dense ceramic. It was found that the inclusion of additives promoting needle‐like microstructures increases the mechanical resistance up to four times the value determined for the ceramic without additives (flexural strength up to 390 MPa for zero‐porosity extrapolation). These results, together with the refractoriness of mullite, allow inferring the potential applications of the developed materials as structural ceramics with relatively low density and for filtering applications.