Pore Volume Distribution Research Articles

Production and optimization of activated carbon from plant waste with high specific surface area for moisture-saving applications in agriculture

In conditions of water shortage, sustainable agricultural development requires the use of water-saving technologies, including the use of water-retaining substrates based on activated carbon. In this work, the textural and adsorption characteristics of activated carbon obtained from plant waste were studied at different mass ratios of the sorbent and KOH (1:1, 1:2, 1:3 and 1:4). The aim of the study was to determine the optimal activation conditions for creating a material with a high specific surface area and a developed porous structure. The results showed that the largest pore volume (1.6 cm3/g) and a high degree of microporosity are achieved at a ratio of 1:3, which is confirmed by the analysis of pore distribution using the DFT and BJH methods. FTIR spectroscopy revealed the presence of functional groups (O–H, C=O and C–O) that contribute to water conservation. The differential pore volume distribution (dv(r), cm3/Å/g) also demonstrated that at a ratio of sorbent and KOH (1:3), the sample structure optimally combines micropores and mesopores, which increases the adsorption capacity of carbon.

Oxidation of Geraniol on Vermiculite—The Influence of Selected Parameters on the Oxidation Process

Geraniol is a compound belonging to the group of monoterpenes that finds many applications in organic syntheses, medicine and cosmetics. The following properties of geraniol and its derivatives are of particular interest in medicine: its anti-inflammatory, antioxidant, antimicrobial and anticancer effects. The geraniol oxidation process was carried out using a mineral of natural origin—vermiculite. Vermiculite is a catalyst that perfectly fits into modern trends in the organic industry, where the aim is to use cheap, renewable and relatively easily available catalytic materials (vermiculite is found on continents including Africa, North America, South America, Australia and Asia). Preliminary studies on the oxidation process of geraniol on vermiculite was carried out in a glass apparatus using molecular oxygen supplied by means of a bubbler and magnetic stirrer with a heating function. During the oxidation process of geraniol on vermiculite, the influence of the following parameters was examined: the temperature, amount of catalyst and reaction time. The main parameters of the process, on the basis of which the most favorable process conditions were selected, were the selectivity of the transformation to 2,3-epoxygeraniol, citral and 2,3-epoxycitral, and the conversion of geraniol. The composition of the post-reaction mixtures was determined qualitatively and quantitatively using the gas chromatography method. In addition, vermiculite was subjected to instrumental tests, such as XRD, SEM, EDX, FTIR and UV-VIS. Moreover, the specific surface area, pore volume and pore volume distribution were estimated on the basis of N2 sorption at −196 °C and also the acid-site concentration in vermiculite was established.

The Correlation Between Compressive Strength and The Size of Pore Fly Ash and Perlite Concrete Geopolymer at High Temperature

Abstract Burned material experiences a decrease in yield strength and elasticity modulus. Fire supervision is required. One of the sustainable material is geopolymer. In this study, fly ash and perlite-based concrete geopolymer have been burned for 900°C for 2 hours. It is followed by Surface Area Analyzer test equipment. The size of pore changes for burned concrete geopolymer. Meanwhile, one of the strength of concrete geopolymer indicator is compressive strength. Both of the results of compressive strength and the pore size are conducted through experimental study. Bet method has been used to measure pore size of it. UTM machine has been used to calculate compressive strength. The surface area analyzer test results show that the addition of perlite to fly ash-based geopolymer concrete will decrease the value of surface area, pore volume, and pore distribution in burned geopolymer concrete, but the addition of perlite to fly ash-based geopolymer concrete will increase the value of pore distribution and decrease the value of surface area and pore volume in unburned geopolymer concrete.

Numerical Analysis of the Influence of Preadsorbed Water on Methane Transport in Crushed Shale

Summary Methane migration in shale is affected by preadsorbed water. To understand this effect, we examined several key parameters, including the effective pore diameter Le, the pore volume distribution of Le, the effective porosity ϕe, the equivalent particle diameter da, and the water film thickness h. Using these parameters, we established an equivalent relationship linking the particle packing da and the Le and the ϕe of the capillary pores within a unit-length cuboid of particles. Based on this relationship, a conceptual model was developed to simulate methane adsorption and transport in partially saturated crushed shale, incorporating parameter estimation for the tangential momentum adjustment factor δ and methane desorption rate coefficient kd, where δ characterizes the slip flow intensity and kd is related to the Langmuir adsorption constant. The finite element method was used to calculate the methane permeability ke, Knudsen diffusion coefficient Dke, surface diffusion coefficient Ds, and adsorption phase transition rate Rm, which are all affected by adsorbed water. The model’s numerical results were validated through comparison with the results from adsorption experiments. These results revealed three distinct regions in the trend of the variation in δ with Le: a rapid increase in Region I (Le < 10 nm), a slowing increase in Region II (10 ≤ Le ≤ 100 nm), and a gradual increase in Region III (Le > 100 nm). In addition, kd is positively correlated with da. kd is also correlated with water saturation S; specifically, kd decreases when S ≤ 12%, increases when S = 12% to 45.8%, and decreases again when S exceeds 45.8%. The results also reveal overall negative correlations between h and ke, Dke, Ds and Rm. Furthermore, the rates of change in ke, Dke, Ds and Rm with increasing ε (ε is the bending coefficient associated with adsorbed water) range from 7.5% to 49.4%. Similarly, ke, Dke, and Ds increase by factors of 0.73–7.19 with increasing χ (χ is the coverage rate of the adsorbed water film). Additionally, as the adsorption time t increases, Ds initially increases rapidly, followed by a gradual increase. Between t = 500 seconds and 1,500 seconds, the rate of change in Ds decreases by 20%. Rm shows a three-stage relationship with t, namely, a rapid decrease from t = 0 seconds to 500 seconds, a steady decrease from 500 seconds to 1,000 seconds, and a stabilization from 1,000 seconds to 1,500 seconds, with Rm ranging from 1.10×10-11 mol/(m3·s) to 9.45×10-11 mol/(m3·s) overall. Ds increases with the adsorption amount ratio Ed (Ed is the ratio of the adsorption amount at t to the equilibrium adsorption amount). As Ed ranges from 0.2 to 0.6, the rate of change in Ds increases by 87% to 100%. Furthermore, Rm is negatively linearly correlated with Ed.

Influence of Supercritical Conditions on Isothermal Adsorption Capacity Calculation of Methane and Model Optimization.

The study of isothermal adsorption models for coal and methane under supercritical conditions helps us to understand the gas content distribution in coal seams and improve gas management in coal mines. Coal samples from the Hebi mine and Longshan coal mine were selected for this research. Using the weight method, isothermal adsorption curves of supercritical methane at temperatures of 308, 313, and 318 K were measured. The adsorption phase density of supercritical methane was obtained by using the intercept method and model fitting, and the absolute adsorption capacity of methane was calculated. Simultaneously, the pore volume and specific surface area of the coal samples were tested, and the isothermal adsorption model for supercritical methane was studied and optimized. The results indicate that using mercury intrusion, low-temperature N2, and low-temperature CO2 adsorption methods for testing coal sample pore structures allows for multiscale characterization of the coal pore structure. Based on the Gibbs excess adsorption theory, the phase density of methane obtained from the intercept method and model fitting effectively represent the isothermal adsorption curve of supercritical methane. By combination of the specific surface area and pore volume distribution of the coal with the absolute adsorption capacity of methane, the number of methane adsorption layers on the coal surface was calculated to be between 1.11 and 1.3 layers. This suggests that the isothermal adsorption model for supercritical methane on coal is not solely micropore filling or single molecular layer adsorption but primarily single molecular layer adsorption with concurrent micropore filling adsorption. Based on this adsorption mechanism, an L-DA isothermal adsorption model for supercritical methane on coal was established. The L-DA isothermal model shows good fitting results and effectively explains the adsorption characteristics of supercritical methane on coal.

Synthesis of high surface area mesoporous ZnAl2O4 with excellent photocatalytic activity for the photodegradation of Congo Red dye

The large-scale release by the textile and other industries of organic dyes into water courses degrades the aquatic environment and results in serious health problems for wildlife, humans, and domestic animals. The removal of such dyes from wastewater is therefore a pressing and important challenge. The efficient photocatalytic destruction of these dyes using sunlight is an elegant and attractive potential solution. In this work, mesoporous ZnAl2O4 nanomaterials were prepared with high specific surface area, high pore volume and uniform pore size distribution using a modified sol–gel synthetic protocol. BET analysis showed that the highest surface area achieved for ZnAl2O4 reached 344 m2/g. The texture, structure and chemical composition of these materials were further studied using XRD, FTIR, TEM, EDS, CHN and XPS analysis and zeta potential measurements. Band gap energies were obtained from UV/vis spectra and showed a strong decrease as particle size decreased, shifting absorption into the visible range for the finest materials and indicating the potential to improve the efficiency of photocatalysis under solar irradiation. Photocatalytic activity was evaluated by studying the photodegradation of Congo Red dye and, for the best materials, showed that 99 % of the dye was degraded in only 30 mins. These results compared very favourably with those of previously reported studies. The degradation products of the Congo Red were further investigated using mass spectrometry and this detailed study confirmed that true photoinduced fragmentation of the dye molecule occurred rather than simple ‘photobleaching’.

Practicability and fundamental performance of alkali treated raw bamboo fiber reinforced high performance seawater sea sand concrete

In pursuit of sustainable development, there has been an increasing amount of research on plant fiber reinforced concrete and seawater sea sand concrete in recent years. In this study, a new type of alkali treated raw bamboo fiber reinforced high performance seawater sea sand concrete (ABFRHPSSC) was suggested, with its practicability evaluated and its fundamental performance investigated. The practicability was evaluated through fiber tensile test, water absorption test, single fiber pull-out test, and degraded fiber characterization test. The fundamental performance, including flowability, mechanical performance, pore volume distribution and three-dimensional distribution of pores and raw bamboo fibers, were then investigated when fiber content and length were used as two parameters. The results showed that the alkali treatment of raw bamboo fibers could increase their tensile strength and elastic modulus, reduce their water absorption, improve their bond performance, and ensure their degradation stability. The fiber content and length had significant effects on the fundamental performance. A fiber content of 0.5 % and a fiber length of 12 mm resulted in relatively optimal mechanical performance while ensuring satisfactory flowability and uniform fiber distribution. At this point, compared with plain high performance seawater sea sand concrete (HPSSC), the compressive, splitting tensile, and flexural strengths increased by 20.1 %, 33.2 %, and 33.6 %, respectively, and the pores were refined. Therefore, ABFRHPSSC has a promising future as a new environmentally friendly material.

Meso-Macroporous Hydroxyapatite Powders Synthesized in Polyvinyl Alcohol or Polyvinylpyrrolidone Media.

Mesoporous hydroxyapatite (HA) is widely used in various applications, such as the biomedical field, as a catalytic, as a sensor, and many others. The aim of this work was to obtain HA powders by means of chemical precipitation in a medium containing a polymer-polyvinyl alcohol or polyvinylpyrrolidone (PVP)-with concentrations ranging from 0 to 10%. The HA powders were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, atomic emission spectroscopy with inductively coupled plasma, electron paramagnetic resonance, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The specific surface area (SSA), pore volume, and pore size distributions were determined by low-temperature nitrogen adsorption measurements, and the zeta potential was established. The formation of macropores in powder agglomerates was determined using SEM and TEM. The synthesis in 10% PVP increased the SSA from 101.3 to 158.0 m2/g, while the ripening for 7 days led to an increase from 112.3 to 195.8 m2/g, with the total pore volume rising from 0.37 to 0.71 cm3/g. These materials could be classified as meso-macroporous HA. Such materials can serve as the basis for various applications requiring improved textural properties and may lay the foundation for the creation of bulk 3D materials using a technique that allows for the preservation of their unique pore structure.

In-situ SANS study on spatial evolution of coal nanoporosity during pyrolysis at elevated temperatures

The nanopore evolution in coal during pyrolysis is vital for optimizing heat and mass transfer in coal conversion processes. Therefore, small-angle neutron scattering (SANS) was utilized to examine the in-situ changes in the nanopore structures of two subbituminous Chinese coal samples during pyrolysis. The nanopore structures were examined in terms of average pore size, pore volume distribution, fractal dimension by SANS at elevated temperatures. Throughout the pyrolysis process, a consistent enlargement of the average size of nanoscale pores was noted as temperatures escalated, with an expansion ranging from 5.3 to 8.2 nm. Particularly during the devolatilization phase (300–500 °C), there was a marked surge in the volume of large pores, exhibiting a growth rate of about 88.1–150.5%. High-temperature (600–800 °C) conditions facilitated the formation of new and smaller pores. While the surface roughness of nanopores experienced a slight reduction throughout the pyrolysis, the directional growth of the pores maintained an isotropic distribution.

Effect of Exposure Conditions on Mortar Subjected to an External Sulfate Attack.

This study aims to investigate the influence of exposure conditions on the behavior of mortar subjected to an external sulfate attack (ESA). Three different exposure conditions (full immersion, semi-immersion, and drying/wetting cycles) were tested on mortar prisms made with Portland cement and two w/c ratios (0.45 and 0.6). To monitor degradation, it was necessary to evaluate variations in length (expansion), mass changes, compressive and tensile strengths, changes in the total porosity measured using water accessible porosity tests, and changes in the macroscopic behavior of the samples. Mercury intrusion porosimetry (MIP) was used to determine the size distribution of the pores. It was demonstrated that mixing mortar with the lower w/c ratio of 0.45 results in improved performance against an ESA. This study also demonstrates that the type of exposure to an ESA has no significant effect on the kinetics of sulfate penetration during the exposure period. However, the sample's surface becomes more cracked when subjected to repeated drying and wetting cycles. For all the considered exposure conditions, expansion occurred in three stages. In stage 1, the reaction product (ettringite) precipitated in large voids, without causing significant expansion (the expansion remained low and stable). During the second stage, the reaction products generated growing internal stress. The final stage of expansion resulted in microcracks, strength losses, and the formation of macropores, which ultimately lead to material failure. The MIP results indicate that major changes in the porosity and pore volume distribution occur at the surface layer in regard to the gel and capillary pore ranges.

Microstructural analysis of the pore size and volume distribution of bentonite at two different hydraulic states utilizing different drying techniques

Bentonite, which is known as adsorbent expansive clay, is widely used as a nanoparticle in a variety of applications due to its unique microstructure. Analyzing the pore size distribution is crucial for studying its microstructural behavior. Drying techniques and initial moisture content play a significant role in the microstructural changes of clays. This study aimed to investigate how different drying techniques and initial moisture content influence the pore size and volume distribution of bentonite. The results indicate a correlation between drying techniques and hydraulic states with the microstructural changes observed in bentonite. Pore size distribution analysis reveals distinct differences in micro, meso, and macro-pore volumes depending on the employed drying techniques. Conventional drying methods show significant alterations in pore volume distribution for specimens prepared with moisture content from dry and wet of the compaction curve's optimum water content. Conversely, a separate phenomenon is observed for specimens subjected to direct outgassing without prior drying. It is observed that specimens undergoing outgassing at elevated temperatures exhibit almost similar pore volume distributions between dry and wet specimens. Dry specimens exhibit a higher cumulative pore volume and a greater number of macro pores compared to wet specimens when subjected to a specific drying method. Moreover, specimens subjected to outgassed freeze-drying, oven-drying, and air-drying exhibit significant changes in cumulative pore volume distribution compared to those without outgassing treatment. These findings highlight the importance of employing a standardized drying technique to accurately predict the microstructural behavior of bentonite clay and understand its pore-size distribution.

The improvement on calcium leaching resistance of high SCMs content cement in ammonium chloride solution using particle gradation technique

Particle gradations of Portland cement (PC), fly ash (FA), and blast furnace slag (BFS) were optimized to improve the calcium leaching resistance of blended cement with high contents (up to 70%)of supplementary cementitious materials (SCMs). The results showed that optimized blended cement showed refined initial pore volume distribution, reduced portlandite (CH) content, finer CH macrocrystals and enhanced stability of C-(A)-S-H gel. Consequently, it displayed exceptional calcium leaching resistance with reduced losses in mechanical performance, mass and pore degradation after calcium leaching. Blended cement with 30% PC (D50 = 14.46 μm), 30% FA (D50 = 10.94 μm), 20% BFS (D50 = 10.52 μm), 13% BFS (D50 = 5.31 μm) and 7% BFS (D50 = 4.71 μm), showing compressive strength retention rate of 79.05% and mass loss rate of 1.64%, was suggested as viable choice for calcium leaching resistant concrete.

Full-Scale Pore and Microfracture Characterization of Deep Coal Reservoirs: A Case Study of the Benxi Formation Coal in the Daning–Jixian Block, China

The pore-fracture structure of deep coal reservoirs is highly important for evaluating, exploring, and developing coalbed methane (CBM) resources. This study considers three coal samples from the DJ57 well in the Benxi Formation in the Daning–Jixian block on the eastern margin of the Ordos Basin as the research object. Based on the coal quality parameters of the coal samples, field emission scanning electron microscopy (FE-SEM), gas adsorption experiments, high-pressure mercury intrusion porosimetry (MIP), and microcomputed tomography (micro-CT) scanning were used to quantitatively characterize the nanoscale pores and microscale fractures in deep coal reservoirs and to evaluate the pore-fracture structure at different scales. The results reveal that the pore types in the Benxi Formation coal samples are diverse and include mainly organic matter (OM) pores, inorganic pores (intraparticle and interparticle pores), and microfractures. The organic pores are diverse in shape and mainly exhibit round, oval, and wedge shapes, while the microfractures exhibit slender stripes or serrated curves. The multiscale quantitative characterization of deep coal reservoir pores and fractures is based on a variety of pore characterization methods, and the pore and fracture volume distributions are mainly U-shaped, revealing the coexistence of micropores and microfractures. The volumes of micropores (0.3–2 nm), mesopores (2–50 nm), macropores (50 nm to 10 μm), and microfractures (>10 μm) account for 78.00%, 6.78%, 2.08%, and 13.14%, respectively, of the total pore volume (PV). Based on a full-scale pore-fracture splicing calculation, the total permeability of the Benxi Formation coal samples ranges from 5.77 to 28.22 mD. The observation results indicate that the microfractures are connected to each other, forming a network structure with strong connectivity. The microfractures are mainly associated with pore diameters>100 μm, accounting for approximately 95% of the total permeability. Moreover, micropores in deep coal reservoirs provide a large space for CBM adsorption, and microfractures enhance the seepage capacity of CBM.

The Removal of Phosphorus from Wastewater Using a Sewage Sludge Biochar: A Column Study

This scientific study investigated the adsorption capabilities of biochar samples derived from municipal sewage sludge pellets. Sewage sludge was pyrolyzed at various temperatures (400, 500, and 600 °C), and the biochar’s properties, including specific surface area, pore volume, and pore size distribution, were assessed. The results indicate that the sewage sludge biochar samples are mesoporous materials with significant potential for good adsorption performance. Despite showing a decrease in specific surface area compared to that achieved with pyrolysis at 400 °C, samples pyrolyzed at 600 °C demonstrated an increase in mesopore surface area, enhancing their adsorption potential. Two filtration experiments, conducted at a flow rate of 8 mL/min, revealed that the column containing sewage sludge pyrolyzed at 600 °C retained phosphorus the most effectively during the first and second experiments (with retention efficiencies of 87% and 78%, respectively). The study concludes that municipal sewage sludge biochar could be a promising material for the removal of phosphorus from wastewater and represents a viable solution for sustainable environmental development.

Evolution of Pore Spaces in Marine Organic-Rich Shale: Insights from Multi-Scale Analysis of a Permian–Pennsylvanian Sample

The quantitative evolution pattern of pore space and genetic pore types along the maturation process in organic-rich shale reservoirs is unclear, which affects the assessment of shale storage capacity and petroleum production. A black shale outcrop sample from Kansas that is of Permian–Pennsylvanian age was collected and subjected to thermal simulation experiments at 10 different maturity stages to understand the pore sizes and pore types. Scanning electron microscopy (SEM) and image processing were used to characterize the full-scale pore-size distribution and volume evolution of this shale sample by combining low-temperature gas (CO2 and N2) physisorption and mercury intrusion porosimetry (MIP) in order to discuss the effects of hydrocarbon generation and diagenesis (HG&D) on pore development at different pore sizes. The study showed that the original shale sample is dominated by slit-like pores, with mainly organic matter (OM) pores distributed in 0–100 nm, intraparticle pores (Intra-P) of clays distributed in 30–100 nm, and interparticle pores (Inter-P) distributed in 100–1000 nm. With the increase in maturity or Ro, the OM pores increased gradually, and the OM pore-size distribution diverged to the two poles. In the oil generation stage, the OM pores were distributed in the range of 30–100 nm, while in the gas generation stage, the OM-hosted pores were mainly distributed in the range of 10–20 nm and 100–500 nm. Further into the over-maturity stage, the OM pores were mainly distributed in the range of 0–10 nm and >100 nm. The pore volume distribution across the whole pore sizes showed that the pore volume of low-maturity shale samples was mainly provided by 100–1000 nm (macropores), and the pore volumes of 0–2 nm, 30–100 nm and 1000+ nm pores gradually increase with increasing thermal maturity, with the final pore-size distribution having four peaks at 0–2, 30–100, 500–1000 nm, and 10–100 µm. Hydrocarbon generation mainly affects the pore volume in the 0–2 nm and 100–1000 nm intervals, with a positive correlation. The 2–30 nm and 30–100 nm pores were likely controlled by diagenesis, such as mineral transformation, illitization, and cementation during the maturation process.

Best practices in the characterization of bulk catalyst properties

Bulk characterization of a solid provides us with a spatially-averaged description of its physical and chemical properties. These properties are not site-specific, but they are critical for categorizing materials and understanding their catalytic performance. Important bulk chemical properties include elemental composition, crystal structure, atomic coordination environment, and the oxidation states of elements comprising the catalyst. Significant physical properties include accessible surface area, pore volume, pore diameter, and particle size distributions that exist at the various length scales of catalysis. Each physicochemical property is sensitive to the conditions employed for catalyst synthesis, storage, pre-treatment, activation, and characterization. Thus, it is imperative that authors fully describe materials and methods in publications as this metadata provides context for observed phenomena and allows others to recreate the exact conditions that are essential for reproducibility. Such protocols are necessary for a meaningful interpretation of differences in catalyst performance observed across laboratories. This perspective article defines bulk characterization, provides guidance on bulk characterization methods, and emphasizes important considerations and best practices. Our aim is to build a more nuanced understanding of catalyst characterization. We hope that awareness and application of the principles outlined herein will improve rigor and reproducibility in catalysis science.

Effect of thermal cycling on the mechanics and microstructure of ultra-high performance concrete

This study investigates the mechanical and microstructural responses of Ultra-High Performance Concrete (UHPC) subjected to a substantial number of thermal cycles upto 300 times from ambient temperature to 60°C. The experimental findings reveal a distinctive pattern of behavior in the static compressive strength, characterized by an initial increase, followed by a subsequent decline, and a subsequent modest resurgence as the thermal cycling progressed. Notably, the peak compressive and flexural strengths were attained after 120 thermal cycles, whereas the maximum dynamic compressive strength was observed after 60 thermal cycles. It is worth highlighting that the dynamic increase factor (DIF) exhibited an inverse trajectory in comparison to the static compressive strength. After 120 thermal cycles, the stress-strain curves under impact loads exhibited pronounced strain softening characteristics, with an oscillation state duration of 250μs, which surpassed that of the ascending and descending phases. The observed variances in macroscopic mechanical properties can be attributed to several pivotal factors, including the quantity of hydration product, the mean chain length (MCL) of the calcium-silicate-hydrate (C-S-H) gel, the distribution of pore volume, and the presence of micro-cracks. This comprehensive examination serves as a valuable theoretical and empirical foundation for advancing the utilization of UHPC in applications subjected to prolonged and intricate thermal conditions.

Mesoporous molybdate-substituted hydroxyapatite nanopowders obtained via a hydrothermal route

In the last decade, mesoporous hydroxyapatite (HA) materials have received much attention regarding environmental applications (including adsorption of soil and water contaminants, films for lithium batteries, catalysts, and support systems for catalysis) and open up ample opportunities regarding biomedical devices and structures. Molybdenum ions may strongly influence catalytic and sorption properties of materials. The present study shows an influence of hydrothermal-synthesis conditions (including temperature and duration of the treatment) on phase composition, textural properties, and morphology of molybdate-containing HA. Powders with high crystallinity manifested Brunauer–Emmett–Teller specific surface area up to 55 m2/g with a pore volume of 0.33 cm3/g. The molybdate-containing HA powders were investigated by chemical analysis, X-ray diffraction, Fourier-transform IR spectroscopy, and transmission electron microscopy. Their specific surface area, pore volume, and pore size distributions were determined by low-temperature nitrogen adsorption measurements, zeta potential was quantified, and electron paramagnetic resonance spectroscopy was performed. The concentration of MoO42− preserving the one-phase state was found, and the impact of hydrothermal treatment mode was analyzed by machine learning using artificial neural networks.

Temporal variability of physical quality of a sandy loam soil amended with compost

AbstractCompost can enhance the soil's ability to retain water, resulting in an overall improvement of soil physical quality (SPQ). The purpose of this study was to evaluate the temporal variability of physical and hydraulic properties of a sandy loam soil amended with a compost obtained from orange juice processing wastes and garden cleaning. The soil water retention curve of repacked soil samples at varying compost to soil ratios, r, was determined at the time of compost embedding (M0) and after six months (M6), and twelve months (M12). Indicators of SPQ linked to soil water retention curve such as air capacity (AC), macroporosity (Pmac), plant available water capacity (PAWC), relative field capacity (RFC) and Dexter S-index (S), were estimated. The effect of compost addiction of the pore volume distribution function was also evaluated.The elapsed time from compost application influenced all SPQ indicators but the maximum beneficial effects of compost amendment were achieved within approximately the first six months. Indicators linked the macro- and mesoporosity (Pmac and AC) decreased with r whereas indicators linked to plant water availability (PAWC and RFC) increased with r. The combined effect of time and rate was statistically observed only for Pmac, PAWC and S.Compost addiction reduced the soil compaction and modified the pore system, as the fraction of structural porosity (i.e., macropores) decreased and the fraction of textural porosity (i.e., micropores) increased. It was concluded that even a single application of compost could have a significant impact on soil water retention and microstructure with positive implications for soil health, precision agriculture and crop productivity.

Microstructural changes in thermochemical heat storage material over cycles: Insights from micro-X-ray computed tomography

This paper studies the effect of successive (de)hydration cycles on the structure of potassium carbonate K2CO3·1.5H2O grains for low-temperature heat storage applications. Such structural changes are caused by exposure of the salt to water vapor or removal of water from it, accompanied by successive swelling and shrinkage. Understanding the material's internal structure is key to predicting its behaviour and optimizing its design. However, due to the simultaneous and persistent occurrence of structural changes and transport mechanisms throughout the process, gaining a complete understanding of the phenomenon can be challenging.Unlike conventional experimental approaches and two-dimensional imaging techniques used for porosity assessment, our study showcases the qualitative and quantitative alterations in the porosity and microstructure of potassium carbonate. This analysis is achieved by using Micro-X-ray computed tomography (Micro-CT). The study focuses on the impact of cycling on grain microstructure, investigating pore volume distribution, radial variation of pore sizes, and density of individual grains. It was noted that the porosity increased from 6.4 % to 19.7 % after seven cycles. Initially, we observed a greater number of pores in the core of the uncycled salt grain. However, after cycling, we noticed a more even distribution, with a higher number of pores in the outer region of the grain, which caused a radial change in porosity. Lastly, this research provides the intrinsic and apparent densities of both non-cycled and cycled potassium carbonate specimens.Micro-CT is a good tool for a better understanding of changes in thermochemical material at a structural level. Calculation of porosity provided a pathway to calculate apparent and intrinsic density. The demonstrated method can be used for a wide range of salt hydrates, enhancing the scope and applicability of this study in the field of low-temperature heat storage applications. Additionally, it gives the measuring parameter needed to calculate energy density and change in volume during the reaction.