Microporous Structure Research Articles

Numerical modelling of CMAS infiltration and dimensionless numbers of anti-infiltration designs of thermal barrier coatings

Resistance to calcium–magnesium–alumina–silicate (CMAS) infiltration and corrosion is a crucial problem for safely applying thermal barrier coatings (TBCs) in advanced aero engines. This work proposes a CMAS infiltration model based on the phase-field method to simulate the CMAS infiltration process in TBCs and analyse the influence factor. Further, a key dimensionless number called relative driving force K=rσcos(θc)tsμϛ2hTC2 was found to determine the CMAS infiltration depth using dimensional analysis. A criterion of K<2 was derived and was considered to be the evaluation standard of TBCs with excellent CMAS infiltration resistance. Based on K minimization, novelty TBCs with microstructure of S-shaped intercolumnar gaps and spherical pores are expected to significantly improve the resistance to CMAS infiltration and corrosion.

Promoting Electricity Production and Cr (VI) Removal Using a Light–Rutile–Biochar Cathode for Microbial Fuel Cells

Microbial fuel cell (MFC) technology holds significant promise for the production of clean energy and treatment of pollutants. Nevertheless, challenges such as low power generation efficiency and the high cost of electrode materials have impeded its widespread adoption. The porous microstructure of biochar and the exceptional photocatalytic properties of rutile endow it with promising catalytic potential. In this investigation, we synthesized a novel Rutile–Biochar (Rut-Bio) composite material using biochar as a carrier and natural rutile, and explored its effectiveness as a cathode catalyst to enhance the power generation efficiency of MFCs, as well as its application in remediating heavy metal pollution. Furthermore, the impact of visible light conditions on its performance enhancement was explored. The X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis validated the successful fabrication of rutile composites loaded with biochar. The maximum current density and power density achieved by the MFCs were 153.9 mA/m2 and 10.44 mW/m2, respectively, representing a substantial increase of 113.5% and 225% compared to the control group. In addition, biochar-supported rutile MFCs showed excellent degradation performance of heavy metal pollutants under light conditions. Within 7 h, the Cr6+ degradation rate reached 95%. In contrast to the blank control group, the removal efficiency of pollutants exhibited increases of 630.8%. The cyclic degradation experiments also showcased the remarkable stability of the system over multiple cycles. This study successfully integrated natural rutile and biochar to fabricate highly efficient cathode photocatalyst composites, which not only enhanced the power generation performance of MFCs but also presented an environmentally sustainable and economically viable method for addressing heavy metal pollution.

Strategies for Mitigating Phosphoric Acid Leaching in High-Temperature Proton Exchange Membrane Fuel Cells.

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) have become one of the important development directions of PEMFCs because of their outstanding features, including fast reaction kinetics, high tolerance against impurities in fuel, and easy heat and water management. The proton exchange membrane (PEM), as the core component of HT-PEMFCs, plays the most critical role in the performance of fuel cells. Phosphoric acid (PA)-doped membranes have showed satisfied proton conductivity at high-temperature and anhydrous conditions, and significant advancements have been achieved in the design and development of HT-PEMFCs based on PA-doped membranes. However, the persistent issue of HT-PEMFCs caused by PA leaching remains a challenge that cannot be ignored. This paper provides a concise overview of the proton conduction mechanism in HT-PEMs and the underlying causes of PA leaching in HT-PEMFCs and highlights the strategies aimed at mitigating PA leaching, such as designing crosslinked structures, incorporation of hygroscopic nanoparticles, improving the alkalinity of polymers, covalently linking acidic groups, preparation of multilayer membranes, constructing microporous structures, and formation of micro-phase separation. This review will offer a guidance for further research and development of HT-PEMFCs with high performance and longevity.

Synthesis and NEXAFS and XPS Characterization of Pyrochlore-Type Bi1.865Co1/2Fe1/2Ta2O9+Δ

A cubic pyrochlore with the composition Bi1.865Co1/2Fe1/2Ta2O9+Δ (space group Fd-3m, a = 10.5013(8) Å) was synthesized from oxide precursors using solid-phase reactions. These ceramics are characterized by a porous microstructure formed by randomly oriented grains of an elongated shape with a longitudinal size of 0.5–1 µm. The electronic state of cobalt and iron ions in oxide ceramics was studied by NEXAFS and XPS spectroscopy. The parameters of the XPS spectra of Bi4f, Bi5d, Ta4f, Co2p, and Fe2p ionization thresholds for a complex pyrochlore were compared with the parameters of the corresponding oxides of the transition elements. The energy position of the XPS-Ta4f and -Ta5p spectra is shifted towards lower energies compared to the binding energy in tantalum(V) oxide by 0.75 eV. According to XPS spectroscopy, bismuth and tantalum cations have the corresponding effective charge of +3 and +(5-δ). The NEXAFS-Fe2p spectrum of ceramics coincides with the spectrum of Fe2O3 in its main spectrum characteristics and indicates the content of iron ions in the oxide ceramics in the form of octahedral Fe(III) ions, and according to the character of the Co2p spectrum, cobalt ions are predominantly in the Co(II) state.

Preparation of CeO2QDs-g-C3N4/C composites and electrochemical determination of aflatoxin B1

The presence of Aflatoxin B1 (AFB1) in food represents a significant threat to human health, leading to the development of cancer. The key factor for effective trace detection technology lies in the utilization of sensor materials that exhibit excellent selectivity and high sensitivity properties. In this study, a successfully synthesis of g-C3N4/C with a high specific surface area uses melamine and houttuynia cordata stem as starting materials. A CeO2QDs-g-C3N4/C composite was prepared by hydrothermally anchoring cerium oxide quantum dots (CeO2QDs) onto the surface of g-C3N4/C, the high redox efficiency of CeO2QDs and the small size limitation effect significantly improve the sensing performance. The composite was characterized by XRD, XPS, SEM, TEM, and N2 adsorption-desorption. The results revealed that, the CeO2QDs-g-C3N4/C composite sensor material exhibited significant advantages with a large specific surface area, a well-defined micropore structure, and abundant reactive sites. In addition, electrochemical activity tests are conducted using EIS, CV, and DPV for the purpose of electrochemical investigations. The CeO2QDs-g-C3N4/C/GCE exhibits exceptional electrocatalytic activity against AFB1, with a wide linear response range of 100–1300 pg ml-1, an impressively low detection limit (LOD) of 6.61 fg ml-1 (S/N = 3), and a sensitivity of 0.985 pg μM ml-1μA-1. Furthermore, the stability, repeatability, and interference experimental response errors all remain below 5 %. It is also noteworthy that, the sensor material demonstrates excellent practicality in AFB1 assays conducted on real samples, which serves to illustrate its immense potential for applications in food safety evaluation.

Microporous tungsten oxide spheres coupled with Ti3C2Txnanosheets for high-volumetric capacitance supercapacitors.

In the contemporary landscape of technological advancements, the burgeoning demand for portable electronics and flexible wearable devices has necessitated the development of energy storage systems with superior volumetric performance. Tungsten oxide (WO3), known for its high density and theoretical capacitance, is a promising electrode material for supercapacitors. However, low conductivity and poor cycling stability are still the key bottlenecks for its application. Herein, a novel composite comprising hollow porous WO3 spheres (HPWS) derived by template method was electrostatic self-assembled on the surface of the Ti3C2Tx nanosheets. The resulting electrodes exhibited ultra-high volumetric capacitance of 1930 F cm-3 at 1 A g-1 and rate capability of 46% at 50 A g-1, attributed to enhanced ion accessibility from microporous structure and electron transport from conductive network of Ti3C2Tx even at a high packing density of 3.86 g cm-3. Utilizing HPWS/Ti3C2Tx as the negative electrode and porous carbon as the positive electrode, the assembled asymmetric supercapacitor achieved an energy density of 31 Wh kg-1 at a power density of 650 W kg-1 with over 107% capacitance retention after 5000 cycles. This work provides a promising approach for developing next-generation supercapacitors with ultra-high volumetric capacitance.

Theoretical investigation on elastic property evolutions of low volume fly ash concrete

AbstractToward expanding the application of fly ash in cement‐based materials, this study proposes a comprehensive study on predicting the elastic properties of low‐volume fly ash concrete, with the replacement levels limited to 30% or less. Unlike conventional ordinary Portland cement concrete, the inclusion of fly ash in concrete brings alterations in properties from both chemical and physical perspectives: (1) the presence of fly ash liberates the alkaline solution that consumes calcium hydroxide to generate secondary calcium silicate hydrate gels; (2) unreacted fly ash particles exhibits a refinement effect on the micropore structure and contributes to forming a denser solid matrix. In order to characterize these effects on the mechanical properties of fly ash concrete, this paper conducts qualitative assessment of hydration reactions and quantitative calculations of volumetric compounds in the material. Utilizing the Mori‒Tanaka scheme, a predictive model is then developed to integrate the hierarchical effects of constituents at multiple scales on the modulus of elasticity of low‐volume fly ash concrete. The reliability of the proposed model is validated through a series of mechanical tests involving various mix designs, as well as comparison with other published test data.

Patterned Ultraslippery Surfaces of Stainless Steel Prepared by Femtosecond Laser Ablation for Directional Manipulation of Liquid Droplets.

Slippery liquid-infused porous surfaces (SLIPS) have promising applications in chip laboratories, nanofriction power generation, and microfluidics due to their excellent properties such as good hydrophobicity and low adhesion. However, the self-driven stability of conventionally lubricated surfaces is not high, and the velocity of liquid droplets is difficult to regulate. This greatly limits the potential applications of SLIPS. A strategy is offered to prepare microporous structures of SLIPS directly on a stainless-steel substrate using femtosecond laser processing technology as the main means to realize exhibiting smoothness to liquids. At the same time, the principle of bionics is utilized, the porous structure of SLIPS is combined with the groove structure of rice leaves, or porous structures are combined with the wedge structure of shorebird beak to prepare the three-dimensional structure of SLIPS. Droplets exhibit significant individual anisotropy on three-dimensional (3D) SLIPS of leaf-like groove stripe structure in rice, enabling the precise control of droplet motion direction. When droplets are transported in wedge-shaped SLIPS with an asymmetric structure, the wedge edge can limit the direction of droplet motion while squeezing the droplet to generate Laplace pressure gradient, which achieves continuous self-driven transport of droplets. In addition, based on the above two processing strategies, an information transfer device is designed: the splicing of the self-driven transport surface with anisotropic topological channels enables the differential drive for liquid transport, which provides the conditions for the information transfer of the droplets. This strategy not only is simple and efficient but also provides new ideas for the effective development of multifunctional SLIPS as well as lab-on-a-chip and microfluidic domains.

Entrapment and Reactivation of Polysulfides in Conductive Amphiphilic Covalent Organic Frameworks Enabling Superior Capacity and Stability of Lithium-Sulfur Batteries.

Inhibiting the shuttle of polysulfides is of great significance for promoting the practical application of lithium-sulfur batteries (LSBs). Here, an imine-linked covalent organic framework@carbon nanotube (COF@CNT) interlayer composed of triazine and boroxine rings is constructed between the sulfur cathode and the separator for polysulfides reception and reutilization. The introduction of CNT imparts the conductor characteristic to the interlayer attributed to electron tunneling in thin COF shell, and creates a hierarchical porous architecture for accommodating polysulfides. The uniform distribution of amphiphilic adsorption sites in COF microporous structure not only enables efficient entrapment of polysulfides while allowing the penetration of Li+ ions, but also provides a stable electrocatalytic channel for bidirectional conversion of active sulfur to achieve the substantially improved capacity and stability. The interlayer-incorporated LSBs deliver an ultrahigh capacity of 1446mAg-1 at 0.1C and an ultralow capacity decay rate of 0.019% at 1C over 1500 cycles. Even at an electrolyte/sulfur ratio of 6µLmg-1, an outstanding capacity of 995mAhg-1 and capacity retention of 74.1% over 200 cycles at 0.2C are obtained. This work offers a compelling polysulfides entrapment and reactivation strategy for stimulating the study on ultra-stable LSBs.

High salinity restrains microplastic transport and increases the risk of pollution in coastal wetlands

Microplastics (MPs) pollution in coastal wetlands has attracted global attention. However, few studies have focused on the effect of soil properties and structure on MP transport in coastal wetlands. Salinity is one of the most pivotal environmental factors and varies in coastal wetlands. Here, we conducted column experiments and employed fluorescent labeling combined with Derjaguin–Landau–Verwey–Overbeek (DLVO) theoretical calculations to reveal the vertical transport behavior of MPs. Specifically, we investigated the influence of five salinity levels (0, 0.035, 0.35, 3.5, and 35 PSU) on MP transport in different coastal wetlands soils and a sand through the X-ray photoelectron spectroscopy and nondestructive computed tomography technique. The results indicated that the migration capability of MPs in soils is significantly lower than in quartz sand, and that the migration capability varies depending on the soil type. This variability may be due to soil minerals and microporous structures providing numerous attachment sites for MPs and may be explained by the DLVO energy barrier of MP-Soil (6568–7767 KT) and MP-sand (5250 KT). Salinity plays a crucial role in modifying the chemical properties of pore water (i.e., zeta potential) as well as altering the soil elemental composition and pore structure. At 0 PSU, the maximum C/C0 of MPs through the sand, Soil 1, and Soil 2 transport columns were 37.86 ± 2.36 %, 23.96 ± 1.71 %, and 3.94 ± 0.68 %, respectively. When salinity increased to 3.5 PSU, MP mobility decreased by over 20 %. Additionally, a salinity of 35 PSU may alter the soil pore distribution, thereby changing water flow paths and velocities to constrain the migration of MPs in soils. These findings could provide valuable insights into understanding the environmental behavior and transport mechanisms of MPs, and lay a solid scientific basis for accurately simulating and predicting the fate of MPs in coastal wetland water–soil systems. We highlight the effect of salinity on the fate of MPs and the corresponding priority management of MPs risks under the background of global climate change.

Hybrid Powder‐Based Additive Manufacturing of Laser‐Induced Graphene 3D Architectures with Tunable Porous Microstructures from Waste Sources of Black Liquor and White Pollution

AbstractMacroscopic 3D‐controllable graphene (3D‐CG) architectures not only retain the intrinsic properties of graphene sheets but also exhibit structural advantages for pollutant adsorption and energy storage. This paper proposes a novel hybrid powder‐based additive manufacturing method to fabricate 3D biomass‐derived laser‐induced graphene (3D B‐LIG) structures with customizable geometries and microporous features. This method utilizes two waste sources as feedstock precursors for sustainable graphene production: “black liquor” (sodium lignosulfonate, NaLS) and “white pollution” (polypropylene, PP). Employing a computer‐aided design process, this method allows for the synchronous creation of various freeform macrostructures, with either identical or variable sections. To optimize the formability and processing efficiency of 3D B‐LIG, systematic studies have been conducted. These studies establish the relationship between processing parameters and the resulting structures by controlling the laser parameters and the mixing ratio of NaLS and PP. By leveraging tunable microporous structures with a maximized specific surface area of 485.3 m2 g−1, 3D B‐LIG demonstrates exceptional performance in pollutant adsorption (with a maximum adsorption capacity of 283.3 mg g−1 for methylene blue) and energy storage (with a gravimetric specific capacitance value of 194.9 F g−1).

Biomorphic porous ceramics obtained by infiltration of a Si-based preceramic polymer into poplar wood templates

In this work, a comprehensive and detailed study about the development and characterization of biomorphic porous SiOC/SiC/Si3N4/C-based ceramics was addressed with an integral approach. The materials were obtained using a novel processing route involving the infiltration of a Si-based preceramic polymer into activated poplar wood templates, thermal curing and N2 pyrolysis. The physical, structural, microstructural, and textural properties mostly depended on the degree of infiltration reached and the pyrolysis temperature used. All the developed porous microstructures exhibited the poplar wood´s features. It is worth noting the development of macropores with confined Si3N4 crystals, and particularly in the samples pyrolyzed at 1500 and 1600 °C, one-dimensional Si-based nanostructures, and micro- and mesopores located in cavity walls and within arrangements of the one-dimensional structures, mainly in the materials pyrolyzed at 1400 and 1500 °C. The last materials presented the highest specific surface area values, thus making them potential candidates in catalysts.

Investigation of high internal phase water-in-oil emulsion on coal gasification fine slag flotation decarburization and its oil saving mechanism

Froth flotation stands as the preferred technique for the separation of charcoal and ash from coal gasification fine slag (CGFS). However, the presence of a well-developed pore structure and an abundance of oxygen-containing functional groups on the surface of residual charcoal necessitates the use of substantial dosage of collectors during the flotation of CGFS. To address this, a high internal phase water-in-oil (HIP W/O) emulsion, with an internal phase water volume fraction of 85 %, was formulated for the flotation decarburization of CGFS, with the objective of reducing the collector dosage. The outcomes of flotation tests demonstrated that at dosages of 50 kg/t for kerosene and 15.04 kg/t for the organic liquid of the HIP W/O emulsion, both were capable of yielding tailings with an ash content exceeding 95 %. The results from Cryo-SEM and viscosity tests suggest that the high viscosity characteristics of the HIP W/O emulsion are primarily attributed to the compact arrangement of emulsion droplets and the active influence of emulsifiers at the oil–water interface. High-speed camera observations revealed that the HIP W/O emulsion droplets exhibited a tendency to disperse into bar-shaped flocs with larger particle sizes in water. This particular dispersion morphology is advantageous for enhancing the oil agglomeration flotation mechanism within the flotation decarburization process of CGFS. LF-NMR tests have further substantiated that the emulsion droplets are not readily absorbed by the microporous structure of the residual charcoal within the CGFS. Wettability tests and FTIR analyses have demonstrated that the hydrophobic modification of the residual charcoal surface, achieved through the HIP W/O emulsion, markedly surpasses that of conventional kerosene. The combination of these results indicates that the use of HIP W/O emulsion in the flotation decarbonization process of CGFS offers multiple benefits. It not only significantly reduces the dosage of organic collectors required, but also enhances the economic efficiency and effectiveness of the flotation process, presenting a novel reagent option for the decarbonization of CGFS.

A Silver Modified Nanosheet Self-Assembled Hollow Microsphere with Enhanced Conductivity and Permeability.

The utilization of sheet structure composites as a viable conductive filler has been implemented in polymer-based electromagnetic shielding materials. However, the development of an innovative sheet structure to enhance electromagnetic shielding performance remains a significant challenge. Herein, we propose a novel design incorporating silver-modified nanosheet self-assembled hollow spheres to optimize their performance. The unique microporous structure of the hollow composite, combined with the self-assembled surface nanosheets, facilitates multiple reflections of electromagnetic waves, thereby enhancing the dissipation of electromagnetic energy. The contribution of absorbing and reflecting electromagnetic waves in hollow nanostructures could be attributed to both the inner and outer surfaces. When multiple reflection attenuation is implemented, the self-assembled stack structure of nanosheets outside the composite material significantly enhances the occurrence of multiple reflections, thereby effectively improving its shielding performance. The structure also facilitates multiple reflections of incoming electromagnetic waves at the internal and external interfaces of the material, thereby enhancing the shielding efficiency. Simultaneously, the incorporation of silver particles can enhance conductivity and further augment the shielding properties. Finally, the optimized Ag/NiSi-Ni nanocomposites can demonstrate superior initial permeability (2.1 × 10-6 H m-1), saturation magnetization (13.2 emu g-1), and conductivity (1.2 × 10-3 Ω•m). This work could offer insights for structural design of conductive fillers with improved electromagnetic shielding performance.

Ultralight activated carbon/polyimide foam with heterogeneous interfaces for improved thermal stability, mechanical properties, and microwave absorption

AbstractThe activated carbon (AC) has been widely used in the field of electromagnetic protection because of its porous, hollow microstructure and excellent electrical conductivity. In this paper, AC was prepared through KOH activation process. The ACs/polyimide foam (PIF) composite was prepared in situ during the synthesis of PI and the ACs. In this paper, AC was prepared using the potassium hydroxide (KOH) activation process. The AC/PIF composites were prepared by mixing ACs and pyromellitic dianhydride (PMDA) with methylene diphenyl diisocyanate (MDI). The pore structure and surface morphology of the ACs were observed using nitrogen adsorption–desorption isotherms and scanning electron microscopy (SEM). After KOH activation with KOH, the surface area and total pore volume of ACs significantly increased by 79.31% and 0.9539 cm3/g, respectively, mainly were the microporous structure. X‐ray photoelectron spectroscopy (XPS) results confirmed an increase in the oxygen content of ACs after KOH activation, indicating an increase in the relative hydroxyl content on the surface. The SEM resulting of the ACs/PIF composite has a well‐developed open cell structure. Thermal gravimetric analysis (TGA) revealed that ACs significantly improved the thermal stability of the ACs/PIF composite. The compressive strength of the ACs/PIF‐3 increased from 518 to 834 KPa, significantly enhancing its mechanical properties. Simultaneously, the microwave absorption performance can be controlled and regulated by optimizing the impedance gradient of the skeleton. Results showed that when ACs constituted 8 wt% of the PIF, the real permittivity (ɛ′) and imaginary permittivity (ɛ″) of ACs‐PIF‐5 were approximately 2.03 and 0.025, respectively.

Review on the Study of Microscopic Pore Structure and Seepage Characteristics

Pore structure, as the focus of researchers, is also one of the main contents of reservoir geological research, and the characteristics of percolation depend on the micro-pore structure of the reservoir. The study of the characteristics of fluid percolation in the reservoir plays an important role in formulating a reasonable oil and gas exploitation scheme. Understanding the micro pore structure of the reservoir, analyzing the pore throat structure inside the oil and gas reservoir, and systematically studying the micro seepage characteristics of the reservoir have far-reaching influence and great significance for the exploration and development of oil and gas fields.

The Phosphonitrilic-derived graphynes as promising adsorbents of greenhouse gases

The new hybrid graphyne-like materials with highly developed specific surface area and excellent greenhouse gas adsorption properties have been described. Inorganic P3N3Cl6 was selected as a building block and 1,4-diacetylene benzene was chosen as a linker for these materials. The chemical structure of P3N3Cl6 allows for creation of three-dimensional materials with the BET surface area ranging from 600 to 1000 m2 g−1 and a pore volume as high as 0.3 cm3 g−1. The obtained materials showed microporous structure and distinctive greenhouse gas adsorption properties. For those materials, CO2 adsorption reached as high as 1.5 mmol g−1, while for N2O ranged from 1.5 to 1.7 mmol g−1, and for CH4 was 0.4 mmol g−1 when adsorption was carried out at 100 kPa and 300 K. Moreover, obtained by the modified Dubinin adsorption model, the maximum adsorption values were 2.5–11 mmol g−1 depending on the type of materials used. This finding suggests that new materials are promising high-pressure adsorbents of greenhouse gases.

Turning coal hydrogenation liquefaction residue into high conductivity carbon black with magnesium citrate-assisted steam activation followed by high temperature treatment

The high conductivity carbon black was prepared using coal hydrogenation liquefaction residue as raw material, through a combination methods of solvent extraction purification, magnesium citrate-assisted carbonization, steam activation, and high-temperature treatment. The effects of carbonization and activation process parameters, heat treatment temperatures, and other factors on the microstructure, specific surface area, degree of graphitization, and conductivity of the carbon black were studied. The coal direct liquefaction residue was firstly purified using a xylene and tetrahydrofuran solution with a volume ratio of 1:1 by centrifugal separation method to obtain coal liquefaction asphalt. Then, the coal liquefaction asphalt was mixed with magnesium citrate in a mass ratio of 3:7 and ball-milled for 90 min. After carbonizing at 950 °C for 120 min, magnesium ions were leached out with hydrochloric acid. The obtained sample was activated with steam at 900 °C for 100 min and then underwent high-temperature treatment at 1500 °C under a N2 atmosphere for 120 min. The microstructure of the conductive carbon black exhibited an irregular blocky structure with an average particle size of 2–10 μm. The specific surface area of carbon material was 579.69 m2/g, with the pore distribution predominantly microporous, accounting for 69.81 % of the total pore volume. It featured a higher degree of graphitization (ID/IG=1.06) and fewer surface oxygen-containing functional groups compared with coal direct liquefaction residue. Electrochemical testing showed that the electrical resistance of the carbon material was only 1.55 Ω, and the reversible capacity under a current density of 1 A/g was 96 mAh/g, which are superior to those of the existing commercial conductive carbon black. The microporous structure and higher degree of graphitization facilitate efficient electron transmission, while the lower content of surface oxygen functional groups effectively reduces electron transfer resistance. This work offers new insights into the structural design and performance enhancement of coal liquefaction residue-derived conductive carbon black functional materials. Furthermore, it has significant implications for the future development of conductive carbon black in energy saving and energy storage.

Comparative study of limestone calcined clay cement produced with mechanically activated kaolin and calcined kaolin

Limestone calcined clay cement (LC3) is a promising solution for mitigating CO2 emissions in cement production by substantially replacing clinker with widely available supplementary cementitious materials. While calcination is the conventional method for activating clay, there is a growing interest in mechanical activation. Incorporating mechanically activated kaolin into LC3 formulation would offer a novel approach to producing this cement. This study aims to assess the impact of replacing calcined clay (CC) with mechanically activated clay (MC) in LC3 properties and relevant features. Accordingly, LC3 with MC substitutions ranging from 0 to 100 wt% were formulated. The resulting cements were characterised to evaluate their physicochemical properties, microstructure, strength, and pore distribution. LC3 incorporating MC exhibited comparable crystalline and amorphous phases to LC3 containing CC. However, the incorporation of MC accelerated hydration, leading to the earlier formation of carboaluminates and consumption of portlandite, alongside enhanced compressive strength at early curing stages. At 28 days, LC3 with 100 wt% of MC displayed similar compressive strength (42 MPa) to LC3 with 100 wt% of CC (40 MPa) with comparable pore distribution and microstructure. These findings validate MC's potential to substitute CC in LC3, offering an alternative for activating clay.

Surface chemistry and catalytic activity in H2O2 decomposition of pyrolytically fluoralkylated activated carbons.

According to the proposed pyrolytic method, granular activated carbon (AC) Norit 830 W was functionalized by thermal treatment of AC in hydrofluorocarbon (HFC) gases, pentafluoroethane and 1,1,1,2-tetrafluoroethane, at 400-800 °C. This method does not require activation by plasma and photons. Chemical and elemental analysis showed that the pyrolytic treatment provides a loading of 2.95 mmol (5.6 wt%) of fluorine per gram of AC. Nitrogen adsorption measurements indicated that the microporous structure contracted when AC was treated with HFC at temperatures above 400 °C. Thermogravimetry, Fourier transform infrared spectroscopy (FTIR) with attenuated total reflectance (ATR), and X-ray photoelectron spectroscopy (XPS) demonstrated the evolution of oxygen-containing and fluorine-containing groups to more thermostable groups with treatment temperature. The fluorine-containing groups grafted at high temperature, above 600 °C exhibited the highest thermal stability up to 1250 °C in dry argon. From the data of XPS and solid-state 19F nuclear magnetic resonance spectroscopy data, the grafted fluorine exists in several types of grafted F-containing groups, the HFC residues. By changing the thermal regime of fluorination, the composition of fluorine-containing groups on a carbon surface can be regulated. Isolated fluoroalkyl groups can be grafted at temperatures of 400-500 °C, while at 600 °C and above, the semi-ionic fluorine groups increase significantly. The hydrophobized surface demonstrated the ability to effectively decompose H2O2 in methanol solutions.