Decrease In Pore Volume Research Articles

Thermochemical heat storage and material behavior of calcium hydroxide fine powder in a fluidized bed reactor

The Ca(OH)2/CaO reaction has attracted much attention in thermochemical heat storage. However, commercial Ca(OH)2 is usually offered as a fine powder that tends to agglomerate in the fluidized bed and affects heat storage performance. The experimental study on these issues is incomplete. In this paper, a fluidized bed thermochemical heat storage test system is built to study the heat storage and release process of Ca(OH)2 fine powder. The experimental results indicate that the water vapor is the primary factor in agglomeration. The increase in heat storage temperature, fluidization velocity, and inlet water flow rate can all reduce reaction time. However, the effect of heat storage temperature on agglomeration is negligible. While a high fluidization velocity can alleviate the agglomeration, a high inlet water flow rate intensifies the agglomeration. The heat storage density decreases by about 12 % after 5 cycles owing to the material loss, while the agglomeration is trending upward. The specific surface area and specific pore volume decrease by 46.59 %, and 13.89 % respectively, which slows down the heat storage process. This work can serve as a reference for alleviating the agglomeration, as well as the operation and adjustment of the fluidized bed.

Influence of in-situ lunar temperature on the pore structure and solid phases of alkali-activated lunar regolith simulant

The construction of extraterrestrial bases has become an indispensable step in the active exploration of deep space. In this study, alkali-activated lunar regolith simulant (AALRS) activated by sodium hydroxide (SH) and sodium silicate (SS) were prepared and then cured at various lunar temperatures. The compressive strength was tested, and the pore structure characteristics were characterized using mercury intrusion porosimetry (MIP), followed by further in-depth quantitative analysis through fractal theory. The solid phases were characterized using thermogravimetry analysis (TGA) and scanning electron microscopy (SEM). It is found that all the fractal curves are divided into three regions, and the fractal dimensions in all regions are between 2 and 3, suggesting the pores of AALRS paste always have self-similar physical significance. The fractal dimension D1 of the small pore is the largest, followed by fractal dimension D3 of the great pore and fractal dimension D2 of the middle pore. The increase in modulus and temperature leads to an increase in the pore surface area, fractal dimension, amount of N-A-S-H gel and compressive strength and a decrease in total pore volume and characteristic pore diameter, which is mainly attributed to the nucleation effect of soluble Si. The turning pore diameter at the micrometer scale and excessive porosity of AALRS paste, which is distinctly different from that of common cementitious materials, demonstrates looser pore structure of AALRS paste. Based on these results, the influence mechanism of in-situ lunar temperature on the performance of AALRS paste is profoundly discussed and elucidated, which provides a deep understanding of designing and tailoring the various properties of AALRS material.

Effect of welding gas mixtures on weld material and bead geometry

Abstract Shielding gas is an essential parameter in welding processes, serves to shield the molten material from the atmosphere and external contaminations while providing a stable electric-arc pathway during the process, thus influencing the quality of the weld bead and several other aspects of the process. Therefore, any welding-based process, such as wire-arc additive manufacturing, could benefit from shielding gas mixture optimisation to selectively improve the processing and possibly the final mechanical properties of the welded material. In this study welding of EN AW 5183 aluminium (single weld bead and wire-arc additive manufacturing build-up) was conducted using several gas mixtures and their influence on final geometry defects, and microstructure measured. The gas mixtures used were a combination of varying amounts of carbon dioxide, nitrogen, and oxygen. These were added to commercially available argon gas. It was observed that: CO2 additions led to an unfavourable bonding defect and increased mean grain size; nitrogen additions caused a decrease in mean grain size, decreased pore count while maintaining a similar pore volume fraction to the reference argon mixture samples; oxygen additions showed slight reduction of mean grain size, decreased pore count and decreased pore volume fraction. These results further showcase that varying shielding gas mixtures influence the final material properties and should be considered as an additional improvement route for conventional welding and additive manufacturing.

On the successful pelletization of a fragile mesoporous material and its mechanical stability mechanism

Mechanical stability is a crucial property for the industrial implementation of heterogeneous catalysts and adsorbents. Both particle size and shape need to be investigated for each application where, typically, a compromise between mass transfer and pressure drop needs to be understood. In this study, we investigate the mechanical stability of a fragile mesostructured cellular foam material, formed of 3D aluminosilicate struts and porous cages, that are connected through windows. Successful pelletization was found at ca. 20 MPa, where the structural and textural properties are either unaltered or minimally modified. This condition is satisfactory for the final application of the pelletized material, though a lower-limit pressure could still be optimized. The use of higher pelletization pressures was observed to increase disorder in the systems. The structure contracts, the cage's size decreases markedly leading to more disordered wormhole-like pores. The decrease in cage/pore size seems to compensate for the structural densification, resulting in relatively constant BET areas. The pore volume's decrease is in agreement with the smaller cage sizes and densification. The damage and the mechanism causing this damage differ from that observed in conventional mesoporous materials. Besides the successful pelletization conditions and identification of damage mechanism, it is also noteworthy to highlight that values for BET area can be misleading when assessing mechanical stability; at high pressures, the BET areas remain fairly constant despite significant changes in pore size and structure are observed.

Design and characterisation of activated magnetic zeolite 4A from naturally occurring kaolin clay of Cameroonian origin for optimised dye removal by Fenton-like degradation

ABSTRACT The transformation of local clay material of Cameroonian origin into magnetic zeolite (Fe@Zeo-4A) for the degradation of acid-blue 90 in solution was investigate herein. The insertion of magnetic iron oxide particles into the zeolitic framework of Zeo-4A was achieved via hydrothermal synthesis. FT-IR spectroscopy, XRD and SEM confirmed the transformation of the clay into zeolite while EDX analysis and elemental mappings confirmed the presence of iron in the magnetic zeolite. Fe@Zeo-4A was strongly attracted to an external magnetic field. N2 adsorption-desorption studies revealed a considerable decrease in specific surface area and pore volume from the zeolite to the magnetic zeolite, suggesting the occupation of the pores of the zeolite by magnetite. The central composite design of the response surface methodology was used as optimisation approach for four parameters affecting the efficiency of degradation: solution pH, H2O2 concentration, initial dye concentration and time of stirring. ANOVA results revealed good correlation between the experimental and predicted results as well as the suitability of the linear regression model for describing the dye degradation process. An adjusted correlation coefficient of 85.17% was obtained for the dye degradation model. An optimal degradation percentage of 95.2% was obtained experimentally under optimal conditions of 7.6 for pH, 20 mg/L for dye concentration, 15.0 mol/L for [H2O2] and 15 min for time, in close agreement with a theoretical response of 96.6% predicted by the model. The magnetic zeolite was found to exhibit good stability over a wide pH range and lost only about 18% of its catalytic efficiency after five cycles of degradation experiments. Therefore, the novel magnetic zeolite-based material is an efficient Fenton catalyst for treating dye-contaminated wastewater.

Deactivation mechanism of NiWS/SAPO-11 catalyst in hydroisomerization of n-hexadecane: Insights into coke deposition behavior and active phase migration

The application of non-noble metal supported catalysts in the hydroisomerization of long-chain n-alkanes is a novel field, and there is currently not any research available on the deactivation process of these catalysts. We investigated into the deactivation mechanism of NiWS/SAPO-11 catalyst in the hydroisomerization of n-hexadecane in this work for the first time. Specifically, coke deposition behavior and active phase migration were investigated. The reduction of catalytic efficiency of the catalyst was partially aided by the decrease in specific surface area, pore volume, and acid density. From the perspective of the active phase, the clusters of NiWS active phase migrated as the reaction time increased, mostly resulting in an increase in both the stacking number and the length of active phase slabs. The migration of active phase increased the distance between active phase clusters and metal sites, and decreased the utilization ratio of active metal atoms. From the perspective of coke deposition, the coke formed on the catalyst includes soft coke and hard coke. The formation and evolution of coke on the catalyst were investigated. The soft coke (aliphatic compounds) progressively transformed into hard coke (polycyclic aromatic hydrocarbons and graphite-like), and the coke gradually migrated from the external surface of the catalyst to the pore channels as the reaction time increased. It is expected to provide theoretical basis and reference value for the deactivation research and design of non-noble metal supported hydroisomerization catalyst.

Structural modification of CNT-C xerogel through synthesis parameters

This study focuses on the synthesis of porous carbonaceous structures by drying resorcinol-formaldehyde (RF) gels under ambient conditions and then carbonizing them in an inert atmosphere. This avoids the expensive drying processes like supercritical drying or freeze drying. However, drying under ambient conditions does cause structural shrinkage and a reduction in porosity and specific surface area. Therefore, the goal of this study was to compensate for these structural degradations by adjusting other synthesis and process parameters, such as solvent exchange, drying condition, content of water, catalyst, and CNT in the gel. In the present study, different organic solvents such as t-butanol, ethanol, and acetone were used to replace the water in the hydrogels at a certain R/F molar ratio (1:2). The experimental results showed that t-butanol, with its low surface tension, resulted in a structure with a high specific surface area and pore volume. Regarding the catalyst dosage, by changing the R/C molar ratio between 71 and 849, the best structural properties were obtained using R/C∼200. Increasing the water content from 15 to 30 mL led to a decrease in specific surface area and pore volume. Drying the gel at an oven temperature of 85 °C resulted in the highest specific surface area, pore volume, and mean pore diameter. Increasing the dosage of carbon nanotubes (CNTs) in the range of 20–150 mg led to an increase in total pore volume and mean pore diameter. The results of this work can be a step forward towards the industrialization of these materials in various applications.

Industrial dye absorption and elimination from aqueous solutions through bio-composite construction of an organic framework encased in food-grade algae and alginate: Adsorption isotherm, kinetics, thermodynamics, and optimization by Box–Behnken design

A potential bio-adsorbent material for removing Rhodamine B (RB) from aqueous solution is Ru-MOF@FGA/CA beads. The adsorption capability of the material is probably enhanced by the use of a natural substance made of food-grade algae (FGA) and calcium alginate (CA), which has been cross-linked and loaded with ruthenium metal-organic frameworks (Ru-MOF). The Ru-MOF@FGA/CA beads were analyzed by XPS, PXRD, FT-IR, and SEM. The nitrogen adsorption-desorption isotherm analysis of the Ru-MOF@FGA/CA beads before and after the adsorption of RB revealed that had a surface area of 682 m2/g, a pore size of 2.92 nm, and a pore volume of 1.62 cc/g, that decreased after adsorption as the surface area reduced to 468.62 m2/g, while the pore volume reduced to 0.76 cc/g. indicating that the RB molecules occupied the available space within the pores of the material. The decrease in both surface area and pore volume specifies that the Ru-MOF@FGA/CA beads' pores were able to effectively adsorb the RB molecules. The adsorption of RB against the Ru-MOF@FGA/CA beads is affected by pH, adsorbent dose, starting RB concentration, and salinity. Controlling these factors can enhance the adsorption capability and effectiveness of the beads for RB removal. With an adsorption energy of 22.6 kJ/mol, the adsorption of RB onto the Ru-MOF@FGA/CA beads was determined to be a chemisorption process, demonstrating a strong bond among the adsorbent and the adsorbate. The pseudo-second-order kinetics and Langmuir isotherms were used to suit the adsorption process. Because the adsorption procedure was endothermic, it increased as the temperature increased. By using this information, the adsorption conditions may be improved, and the beads' ability to absorb RB can be increased. Up to six reuses of the Ru-MOF@FGA/CA beads are possible without affecting their chemical makeup and maintaining analogous PXRD and FT-IR data after each reuse. The adsorption process can be optimized through the application of the Box–Behnken design (BBD) approach and may entail H-bonding, electrostatic forces, n-π stacking, and pore filling. The exceptional stability of the beads makes them useful for creating long-lasting and efficient adsorbents that remove contaminants from water.

Study on the pore blocking characteristics and cleaning methods of permeable asphalt mixtures based on accelerated clogging simulation experiments

Clogging in permeable asphalt pavements compromises their functional properties. Understanding clogging characteristics and developing appropriate maintenance methods is crucial. This study integrates indoor accelerated clogging simulations with Grey Relational Analysis to investigate the factors influencing clogging behavior. Computer tomography scanning and seepage model simulations are utilized to examine the distribution of clogging materials, seepage properties, and changes in pore parameters in permeable asphalt mixtures before and after clogging. Additionally, variable frequency vibration tests are conducted to evaluate the impact of vibration frequency on clog removal efficiency. Findings show that the cementation hardening effect of clay progressively seals pores, with sand particles of 0.15 mm diameter exerting the most significant influence on clogging. Wet-dry cycles lead to an accumulation of clay cementation, resulting in a 26.1 % and 72.4 % decrease in pore channel length and volume, respectively, at depths of 0–4.2 cm. The area within this depth range is most prone to clogging, increasing pore tortuosity. Seepage behavior is primarily determined by several main interconnected pores. Vibration test outcomes indicate that frequencies between 100 and 400 Hz are optimal for disrupting cementation blockages.

Hydrogen-rich syngas upgrading via CO2 adsorption by amine-functionalized Cu-BTC: the effect of different amines.

Syngas produced from supercritical water gasification typically contain a high amount of CO2 along with H2. In order to improve the quality of syngas, amine-functionalized copper benzene-1,3,5-tricarboxylate (Cu-BTC) was synthesized as an effective adsorbent for selective removal of CO2 from syngas to increase the concentration of H2. The amines used in this study included monoethanolamine (MEA), ethylenediamine (EDA), and polyethyleneimine (PEI). The fundamental physicochemical character of adsorbents, CO2 adsorption capacity, and CO2/H2 selectivity were analyzed. The physicochemical characterization indicated that the structure of amine-functionalized Cu-BTC was partially damaged, which resulted in a decrease in specific surface area and pore volume. On the other hand, the enlarged pore size was beneficial for the mass transfer of gas in the adsorbent. Among these adsorbents, Cu-BTC/PEI exhibited the maximum CO2 adsorption capacity of 3.83mmol/g and the highest CO2/H2 selectivity of 19.74. It was found that the adsorption pressure is the most significant factor for the CO2 adsorption capacity. Lower temperature and higher pressure were favored for CO2 adsorption capacity and CO2/H2 selectivity, so physical adsorption by Cu-BTC played a dominant role. Moreover, Cu-BTC/PEI can be well-regenerated with stable adsorption efficiency after five consecutive cycles. These findings suggested that Cu-BTC/PEI could be a promising alternative adsorbent for CO2 capture from syngas.

COMPARISON OF PHYSICAL CHARACTERISTICS OF HIGHLY POROUS MATERIALS DURING THEIR ACOUSTIC AND TRADITIONAL DRYING

A comparison was made of drying fine-porous silica gel grains in an acoustic-convective dryer of the ITAM SB RAS with convective drying in an air atmosphere at normal pressure and with a residual pressure of the furnace working chamber p = 10 -3 MPa. Changes in the morphology, structure, specific surface area, total pore volume and mechanical properties of the original, moistened and dried silica gel grains were recorded. It is shown that when the acoustic-convective drying mode used in the work occurs, intensive extraction of moisture from the sample occurs, which is accompanied by dehydration of the grain fragments of grains are observed, macrodefects in the form of chips are found on the surface of the grains, main cracks are present in the structure of the material, the specific surface area decreases to 200 m2/g, a decrease in the total pore volume to 0:26 m3/g, or the absence of pores smaller than 100 nm, the mechanical strength of silica gel decreases to 96.25%.

PREPARATION AND CHARACTERIZATION OF BENTONITE CLAY CATALYSTS FOR TRANSESTERIFICATION OF WASTE COOKING OIL INTO BIODIESEL

The development of low-cost green catalytic materials is crucial for the conversion of non-edible vegetable oils or waste materials into biodiesel. The research focuses on the preparation and characterization of aluminium pillared clay and NaOH-doped bentonite clay catalysts for biodiesel production from waste cooking oil using XRF, XRD, FTIR and N2 adsorption-desorption techniques. The molecular profile and functional group assessment of the biodiesel were done using GC-MS and FTIR respectively. XRF analysis revealed the presence of oxides in all samples. The amount of SiO2 in all samples was within the range of 35.303–39.199 wt%. Al2O3 increased from 15.560 to 19.11 wt%, while the interlayer cations decreased after pillaring. FTIR revealed the appearance of peaks which are characteristic of bentonite. The pillaring and impregnation of NaOH with bentonite led to a distortion of certain peaks' intensity, as evidenced by FTIR results. The pillaring caused an increase in BET surface area and pore volume compared to bentonite from 302.1 to 366.4 m2/g, and 0.186 to 0.189 cc/g respectively, while a decrease in surface area and pore volume was observed in NaOH/bentonite due to impregnation. The XRD data have shown the increase of basal d-spacing of pillared clay from 12.65 to 16.49 Å relative to bentonite with a decrease to 12.45 in the case of NaOH/bentonite. The catalysts prepared outperformed neat bentonite with NaOH/bentonite, resulting in the highest yield of (83 ± 1.80). GC-MS, FTIR, and physicochemical analyses confirmed the production of fatty acid methyl esters.

STUDY OF CATALYTIC BEHAVIOURS OF THE SPINEL STRUCTURE NdxMg1- xAl2O4 COMPOSITION WITH ZSM-5 ZEOLITE IN ETHYLBENZENE DISPROPORTIONATION

Nanosized (10–15 nm) powders of spinel structures NdxMg1–xAl2O4 were obtained by low-temperature combustion of aluminium, magnesium, neodymium nitrate solutions, diethylmalonate, and hydrazine monohydrate with further calcination of nanopowders at 1000 °C, which were used in the preparation of catalytic compositions with ZSM-5 zeolite. The obtained catalytic compositions were characterized by X-ray diffraction, pyridine adsorption, and low-temperature nitrogen adsorption. The acidic properties and porosity of the catalysts were altered by controlling the concentration of nanopowder (1.0–7.0 wt.%) in the catalytic composition. The interaction of the modifier with HZSM-5 zeolite leads to a decrease in specific surface area and pore volume, as well as reduse of strong Bronsted acid sites (B) and an increase in the concentration of medium Lewis acid sites (L), resulting in a change in the B/L ratio from 3.61 to 0.23. The ongoing variations contributed mainly to an enhancement of the para-selectivity of the catalytic composition in the ethylbenzene disproportionation reaction. The catalytic composition of 5% Nd0.1Mg0.9Al2O4 with a pore volume of 0.15 cm3/g and an acid site B/L ratio of 0.27 demonstrates a maximum selectivity to p-diethylbenzene of 75.6% with a conversion of ethylbenzene of 23.7%.

Quantitative sulfur poisoning of nanocrystal PtO2/KL-NY and its deactivation mechanism for benzene catalytic oxidation

The present study involved the synthesis of a kaolin-based NaY zeolite (KL-NY) supported nanocrystal PtO2 (5–10 nm) catalyst, which exhibited complete benzene conversion at 195 °C. However, a certain amount of sulfur species led to severe deactivation of the catalyst. This deactivation was mainly caused by the reduction of active lattice oxygen. XPS, H2-TPR and HRTEM results confirmed that adsorbed sulfur species competitively consumed active lattice oxygen, resulting in a transition of partial PtO2 to PtO. Generated PtO cannot actively participate in the oxidation reaction due to its weaker oxidation property, indicating a decrease of active species induced by sulfur poisoning. Furthermore, Al2O3 outside the KL-NY framework can adsorb sulfur species and form Al2(SO4)3, leading to an increase in acid sites. Due to the weak acid-tolerance of KL-NY, partial porous structure destruction occurred with a decrease in specific surface area and pore volume, thereby negatively impacting catalyst performance.

Important role of pore-filling mechanism in separating naproxen from water by micro-mesoporous carbonaceous material.

Commercial micro-mesoporous carbonaceous material (MCM; 56.8% mesopores) was applied for investigating the removal phenomenon of naproxen drug in aqueous solutions through batch adsorption experiments. Results demonstrated that the adsorption capacity of MCM to naproxen was slightly affected by different pHeq (2.0-11) and ionic strength (0-1M NaCl). Adsorption kinetics, isotherms, thermodynamics, and mechanisms were evaluated at pH7.0. Adsorption kinetics indicated the rate constants for adsorption (0.2 × 10-3 L/(mg × min) and desorption (0.076/min) and the adsorption equilibrium constant (2.6 × 10-3 L/mg). Adsorption isotherm showed that MCM exhibited a high-affinity adsorption capacity to naproxen (even at low concentrations) and its Langmuir maximum adsorption capacity (Qmax ) was 252.7mg/g at 25°C. Adsorption thermodynamics proved that the adsorption process was endothermic and physisorption (ΔH° = 9.66 kJ/mol). The analysis result of pore size distribution demonstrated that the internal pore structure of MCM was appropriate for adsorbing naproxen molecules. Pore-filing mechanism (pore diffusion phenomenon) was confirmed by a considerable decrease in BET-surface area (585 m2 /g) and total pore volume (0.417 cm3 /g) of MCM after adsorbing naproxen (~1000 mg/L and pH7.0) at 5min (341 and 0.256), 60 min (191 and 0.205), 120 min (183 and 0.193), 360 min (144 and 0.175), and 24 h (71.6m2 /g and 0.123 cm3 /g, respectively). The pore diffusion occurred rapidly (even at the initial adsorption period of 5min). The FTIR technique was applied to identify the existence of C-H···π and n-π interaction. π-π interaction (evaluated through ID /IG ratio and C=C band) played a minor contribution in adsorption mechanisms. The ID /IG ratio (determined by the Raman technique) of MCM before adsorption (1.195) was similar to that after adsorption (1.190), and the wavenumber (C=C band; its FTIR spectrum) slightly shifted from 1638 to 1634 cm-1 after adsorption. A decrease in the Qmax value of MCM from 249 to 217 (H2 O2 -oxidized MCM) or to 224 mg/g (HNO3 -oxidized MCM) confirmed the presence ofπ-π interaction. Electrostatic attraction was a minor contribution. MCM can serve as a promising material for removing naproxen from water environment through a pore-filling mechanism. PRACTITIONER POINTS: Pore-filling mechanism was proposed by comparing textural properties of MCM before and after adsorbing naproxen. C-H···π and n-π interactions were identified via FTIR technique. π-π interaction was observed by FTIR and Raman techniques. Oxidation of MCM with HNO3 or H2 O2 was a helpful method to explore π-π interaction. Electrostatic attraction was explained through studies: effects of pH and NaCl along with desorption.

Structural and sorption characteristics of an aerogel composite material loaded with flufenamic acid: insights from MAS NMR and high-pressure NOESY studies.

The structural and sorption characteristics of a composite material consisting of a silica aerogel loaded with flufenamic acid were investigated using a variety of nuclear magnetic resonance techniques. The composite structure was analyzed using magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy, which revealed significant interactions between the aerogel matrix and the FFA molecules. Solid-state 29Si NMR provided insights into the aerogel's stability, while 1H and 13C NMR confirmed the presence of FFA in the matrix, with signals from FFA molecules observed alongside tetraethoxysilane (TEOS) groups. Ethanol-induced desorption of FFA led to narrowed spectral lines, suggesting the breaking of intermolecular hydrogen bonds. 19F MAS NMR spectra indicated changes in FFA local environments upon loading into AG pores. Evaluation of CO2 sorption characteristics using 13C NMR demonstrated a slower sorption rate for AG + FFA than that for pure AG, attributed to decreased pore volume. Furthermore, nuclear Overhauser effect spectroscopy (NOESY) was employed to explore the conformational behavior of FFA within the aerogel matrix. The results indicated a shift in conformer populations, particularly those related to the rotation of one cyclic fragment relative to the other. These findings provide insights into the structural and sorption characteristics of the AG + FFA composite, which are valuable for developing novel drug solid forms.

Ordered mesoporous silicas for potential applications in solid vaccine formulations

In an effort to develop efficient vaccine formulations, the use of ordered mesoporous silica (SBA-15) as an antigen carrier has been investigated. SBA-15 has required properties such as high surface area and pore volume, including narrow pore size distribution to protect antigens inside its matrix. This study aimed to examine the impact of solvent removal methods, specifically freeze-drying and evaporation on the intrinsic properties of an immunogenic complex. The immunogenic complexes, synthesized and incorporated with BSA, were characterized by various physicochemical techniques. Small Angle X-ray Scattering measurements revealed the characteristic reflections associated to pure SBA-15, indicating the preservation of the silica mesostructured following BSA incorporation and the formation of BSA aggregates within the macropore region. Nitrogen Adsorption Isotherm measurements demonstrated a decrease in surface area and pore volume for all samples, indicating that the BSA was incorporated into the SBA-15 matrix. Fluorescence spectroscopy evidenced that the tryptophan residues in BSA inside SBA-15 or in solution displayed similar spectra, showing the preservation of the aromatic residues’ environment. The Circular Dichroism spectra of BSA in both conditions suggest the preservation of its native secondary structure after the encapsulation process. The immunogenic analysis with the detection of anti-BSA IgG did not give any significant difference between the non-dried, freeze-dried or evaporated groups. However, all groups containing BSA and SBA-15 showed results almost three times higher than the groups with pure BSA (control group). These facts indicate that none of the BSA incorporation methods interfered with the immunogenicity of the complex. In particular, the freeze-dried process is regularly used in the pharmaceutical industry, therefore its adequacy to produce immunogenic complexes was proved Furthermore, the results showed that SBA-15 increased the immunogenic activity of BSA.

Reformation of coal reservoirs by microorganisms and its significance in CBM exploitation

The study investigates the variations in surface morphology and micro-nano-scale pore structure of coal matrix during the process of biodegradation. Comprehensive reservoir characterization techniques, including field emission scanning electron microscope, mercury intrusion porosimetry, and low-temperature N2 adsorption, are employed on four anthracite samples. The significance of the relationship between coal reservoir bio-reformation and coalbed methane (CBM) exploitation is proposed. The main findings indicate that organic matter on the surface of the coal matrix can undergo biodegradation, resulting in the generation of new pores. Microbial metabolism does not alter pore type but only modifies pore size and volume of coal. After microbial degradation, there is an increase in average pore width, while both Brunauer-Emmett-Teller specific surface area and Barrett-Joyner-Halenda pore volume decrease. Furthermore, bioconversion leads to a reduction in both surface and volume dimensions of coal, resulting in a smoother coal matrix surface and simplified complexity of its pore structure. This benefits desorption, migration, and exploitation of CBM. These findings further reinforce the pivotal role of microbial-enhanced coalbed methane production technology in improving CBM production and promoting the clean utilization of coal resources.

Drying shrinkage inhibition effect and mechanism of polyol shrinkagex reducing admixture on the metakaolin-based geopolymer

Geopolymers, environmentally friendly materials, face application limitations due to their high drying shrinkage and propensity for cracking. The shrinkage reducing admixture (SRA) has shown promise in mitigating drying shrinkage in cement-based materials, yet its impact and mechanism in geopolymers remain uncertain. This study examines the influence of the small molecule polyol SRA-2-methyl-2,4-pentanediol on metakaolin-based geopolymer (MKG) properties and its multiscale structural development, aiming to understand the drying shrinkage behavior. The findings reveal that SRA significantly curbs the drying shrinkage of MKG while also reducing its mechanical properties. Analyses of macroscopic and microscopic properties indicate that while SRA does not alter the hydration products of MKG, it can impede the hydration process, particularly in the early stages. Specifically, SRA inhibits the formation of N-A-S-H gel, thereby reducing shrinkage caused by late-stage polycondensation. Furthermore, the alkaline environment in MKG aids SRA in lowering pore solution surface tension and increasing its contact angle, reducing drying shrinkage forces. Additionally, SRA modifies MKG's micro-structure, decreasing pore volume, particularly in the 10–50 nm range, further mitigating shrinkage due to surface tension.

Effect of drying method on calcium silicate hydrate (C-S-H): Experiments and molecular dynamics simulations study

Terminate hydration and drying procedures were necessary before characterizing the cement-based materials. This study investigated the influence of drying method (-including freeze-drying and vacuum-drying) on the composition-structure of main hydration product (C-S-H) in cement-based materials. In addition, the effect of pH value was considered. The in-situ atomic scale change of C-S-H under different drying conditions was described using molecular dynamics simulations (MDS). The results reveal that freeze-drying has a stronger drying effect than vacuum-drying. Freeze-dried C-S-H samples have lower bound water content, smaller interlayer distance, longer mean chain lengths (MCL), denser pore structure and lower crystallinity than vacuum-dried samples. As the pH values increase, the bound water content, interlayer distance, MCL and cumulative pore volume decrease. In addition, although the micromorphology of freeze-dried samples is similar to vacuum-dried ones, the crystallinity of freeze-dried samples is lower than that of vacuum-dried samples. MDS provides evidence for the influencing mechanism of drying method on interlayer distance and chain length of C-S-H from the atomic scale. It also proves that the complexation between water molecules and interlayer Ca2+ is more accessible to be destroyed in freeze-drying than vacuum-drying, resulting in a higher reduction of interlayer distance after freeze-drying. Furthermore, water loss due to drying action breaks the Ca-OH bond, enhances Ca2+ movement in the interlayer of C-S-H and facilitates the generation of Ca-O structure in the interlayer, leading to the increase in chain length of C-S-H.