Search Results (46)

Sorption isotherms enable postharvest technologists to estimate the degree and rate of drying of agricultural produce. They are also useful in the design and operation of desiccant systems that are used to condition air. However, the published data on sorption isotherms contain several inconsistencies. For example, under the conditions considered in this work, it is shown that the widely cited Chung–Pfost isotherm predicts moisture contents of canola that are less than zero as the relative humidity tends to zero. Furthermore, it is shown that a long-established form of empirical expression appears to grossly overestimate the differential heat of wetting, hence the integral heat of wetting of canola. In this work, algebraic expressions are derived that enable the relationship between the forms of isotherm equations on the speed of drying to be calculated. Prima facie, it is anticipated the heat of adsorption will augment the speed of temperature waves through beds of drying canola. However, it is found that this may not be the case. Anomalies in published isotherms for agricultural produce reinforce the need for accurate psychometric data to be measured over a wide range of temperatures and relative humidities. Full article

Ion-adsorption-type rare-earth element (iREE) deposits, a primary source of global heavy REE (HREE) ores, have attracted wide attention worldwide due to their concentrated distributions and irreplaceable role in the field of cutting-edge technologies. In recent years, iREE mineralization has been reported in the overlying weathering crust of the Mosuoying granites within the Dechang counties, Sichuan Province, Southwest China, suggesting great potential for the formation of iREE deposits. The Mosuoying granites, acting as the primary carrier of REE pre-enrichment, govern the contents and distribution patterns of REEs in their weathering crust. Therefore, investigating the sources and enrichment mechanisms of REEs in the parent rocks will provide a critical theoretical basis for the scientific exploitation and utilization of iREE deposits. In this study, we investigated the migration and enrichment of REEs in the Mosuoying granites (850–832 Ma) using petrography, geochronology, geochemical, and Sr-Nd-Hf isotopic data. The results reveal that the REE enrichment in the Mosuoying granites might be associated with both the melting of crustal felsic rocks and the magmatic-hydrothermal evolution. On the one hand, the granites exhibit different REE patterns. Compared to the light REE (LREE)-rich granites, the HREE-rich granites feature higher SiO₂ contents, higher differentiation index (DI), lower Nb/Ta and Zr/Hf ratios, and more significant negative Eu anomalies, indicating that the crystal fractionation of magmas governed the differentiation of REEs. Furthermore, the hydrothermal fluids further promoted the formation of the HREE-rich granites. On the other hand, the geochemical characteristics suggest that they are A-type granites. Regarding the isotopic characteristics, the Mosuoying granites exhibit negative whole-rock εNd(t) and zircon εHf(t) values, suggesting an evolved crustal source. Therefore, we suggest that the high REE contents in the Mosuoying A-type granites might originate from the partial melting of felsic rocks in a shallow crustal source under high-temperature and low-pressure conditions. Specifically, the high-temperature A-type granitic magmas caused the partial melting of the felsic crustal materials to release REEs; concurrently, these magmas enhanced the solubility of REEs in melt during magmatic evolution, inhibiting the separation of REE-bearing minerals from the melts. These increased the REE contents of the granites. The high-temperature heat source might be associated with the process where the asthenospheric mantle experienced upwelling along slab windows and heated continental crust in the Neoproterozoic extensional setting. Full article

The glycine nitrate procedure (GNP) is a method that proved to be the easiest and most effective method for controlling the composition and morphology during the synthesis of Co_0.9R_0.1MoO₄ (R = Ho, Yb, Gd). This method of the combustion process achieves control of stoichiometry, homogeneity, and purity. Metal nitrates and glycine were mixed in the appropriate stoichiometric ratios to produce Co_0.9R_0.1MoO₄ (R = Ho, Yb, Gd). The samples obtained by the mentioned method were further subjected to different characterization methods such as differential thermal analyses (DTA), X-ray diffraction (XRD), Fourier transform infrared spectrum (FTIR), spectroscopy, field emission scanning electron microscopy (FESEM), and nitrogen adsorption method. A high level of anisotropy of the shape and size of particles in the form of agglomerates was found. Also, there are noticeable differences in the microstructure and plate crystals. The color of the synthesized sample changes from darker to lighter shades after thermal treatments. There are pronounced changes in the dominant wavelength (nm) and color purity between the initial sample and the sample after heating (1100 °C) due to the concentration of Co. Full article

The adsorption and reaction of nitric oxide (NO) molecules on the surface of the model-supported metal/oxide system, consisting of Ni nanoparticles deposited on α-Al₂O₃ (0001) in ultra-high vacuum, have been studied using in situ surface-sensitive techniques and density functional theory (DFT) calculations. As a combination of X-ray and Auger electron spectroscopy (XPS, AES), Fourier-transform infrared (FTIR) spectroscopy, and temperature-programmed desorption (TPD) techniques reveals, there is a threshold of Ni particle mean size (<d>) of c.a. 2 nm, differentiating the electron state of adsorbed NO molecules and their reaction. The main feature of Ni particles normally not exceeding 2 nm is that the NO adsorbs in the form of (NO)₂ dimers, whereas, for larger particles, the NO molecules adsorb in the form of monomers, usually characteristic for the bulk Ni substrate. This difference is demonstrated to be the main reason for the different reaction of NO molecules on the surface of Ni/alumina. The striking feature is that, in the case of ultra-small Ni particles (<d> ≤ 2 nm), the nitrous oxide (N₂O) molecules are formed upon heating as a result of the NO self-reduction mechanism, which are otherwise not formed in the case of larger Ni particles. According to DFT results, this is due to the significant synergistic impact of NO co-adsorption on the neighboring NO dissociation reaction over ultra-small Ni particles, mediated by the metal/oxide perimeter interface. The observed molecular conversion effects offer an opportunity to tune the catalytic selectivity of this and related metal/oxide systems via varying the supported metal particle size. Full article

This study aimed to investigate the impact of physical treatments, namely heat (70 °C for 48 h), atmospheric cold plasma (10 kW for 20 min), and ultrasonic frequency (40 kHz for 15 min), on the physicochemical and interfacial properties of soy protein isolate (SPI) and whey protein isolate (WPI) in the context of oleogel production by foam template (cryogel) method. The physical modification of both SPI and WPI was monitored using SDS-PAGE, Fourier transform infrared spectroscopy (FTIR) spectroscopy, and differential scanning calorimetry (DSC), measuring interfacial tension, color, solubility, foam volume, foam stability, and, finally, the density and oil absorption of the produced cryogel. The findings revealed that the application of ultrasonic waves resulted in a significant reduction in the content of alpha-helical of SPI and WPI while the other treatments increased the content of random coil proteins. FTIR analysis further showed that ultrasonic and heat treatment led to a decrease in C-N tensile vibration within the range of 1200–1650 cm⁻¹ in SPI. Meanwhile, in cold plasma treatment, an increase was observed which was confirmed by the elevation of enthalpy from 100 to 128 kJ/kg. Physical treatments significantly altered the surface properties of both SPI and WPI, where this value was reduced in SPI and increased in WPI. The cold plasma method demonstrated superior performance in enhancing the solubility of SPI from 10 to 58.2%, while the solubility of WPI decreased from 96.4 to 90.4%. By modifying the proteins, the foam volume and oil adsorption ability of the related cryogel improved, as shown by the maximum oil absorption obtained after ultrasonic treatment for SPI (11.6 g/g) and cold plasma (9.17 g/g) for WPI. These results could be useful in applying physical treatments to modify proteins and create the cryogel as an oleogel template for structuring liquid oil and producing innovative health value-added foods. Full article

The mass content of expanded graphite (EG) in fatty acid/expanded graphite composite phase-change materials (CPCMs) affects their thermal properties. In this study, a series of capric–myristic acid/expanded graphite CPCMs with different EG mass content (1%, 3%, 5%, 8%, 12%, 16%, and 20%) were prepared. The adsorption performance effect of EG on the PCMs was observed and analyzed. The structure and thermal properties of the prepared CPCMs were characterized via scanning electron microscopy, differential scanning calorimetry, thermal conductivity measurements, and heat energy storage/release experiments. The results show that the minimum mass content of EG in the CPCMs is 7.6%. The phase-change temperature of the CPCMs is close to that of the PCMs, at around 19 °C. The latent heat of phase change is equivalent to that of the PCM at the corresponding mass content, and that of phase change with an EG mass content of 8% is 138.0 J/g. The CPCMs exhibit a large increase in thermal conductivity and a significant decrease in storage/release time as the expanded graphite mass content increases. The thermal conductivity of the CPCM with a mass content of 20% is 418.5% higher than that with a mass content of 5%. With an increase in the EG mass content in CPCMs, the heat transfer mainly transitions from phase-change heat transfer to thermal conductivity. Full article

Melissa officinalis is an important medicinal plant that is used and studied intensively due to its numerous pharmacological effects. This plant has numerous active compounds with biomedical potential; some are volatile, while others are sensitive to heat or oxygen. Therefore, to increase stability and prolong biological activities, the natural extract can be loaded into various nanostructured systems. In this study, different loading systems were obtained from mesoporous silica, like Mobile Composition of Matter family (MCM) with a hexagonal (MCM-41) or cubic (MCM-48) pore structure, simple or functionalized with amino groups (using 3-aminopropyl) such as triethoxysilane (APTES). Thus, the four materials were characterized from morphological and structural points of view by scanning electron microscopy, a BET analysis with adsorption–desorption isotherms, Fourier-transform infrared spectroscopy (FTIR) and a thermogravimetric analysis coupled with differential scanning calorimetry. Natural extract from Melissa officinalis was concentrated and analyzed by High-Performance Liquid Chromatography to identify the polyphenolic compounds. The obtained materials were tested against Gram-negative bacteria and yeasts and against both reference strains and clinical strains belonging to Gram-positive bacteria that were previously isolated from intra-hospital infections. The highest antimicrobial efficiency was found against Gram-positive and fungal strains. Good activity was also recorded against methicillin-resistant S. aureus, the Melissa officinalis extract inhibiting the production of various virulence factors. Full article

Nanomaterials have been the focus of intense study and growth in the modern era across the globe because of their outstanding qualities, which are brought about by their nanoscale size; for instance, increased adsorption and catalysis capabilities plus significant reactivity. Multiple investigations have verified the fact that nanoparticles may successfully remove a variety of pollutants from water, and, as a result, they have been utilized in the treatment of both water and wastewater. Therefore, the current research intent is to examine the nonlinear heat source/sink influence on the 3D flow of water-based silver nanoparticles incorporated in an Eyring–Powell fluid across a deformable sheet with concentration pollutants. Silver particles have been used intensively to filter water, due to their potent antibacterial properties. The leading equations involving partial differential equations are renewed into the form of ordinary ordinary differential equations through utilizing the appropriate similarity technique. Then, these converted equations are solved by utilizing an efficient solver bvp4c. Visual displays and extensive exploration of the different impacts of the non-dimensional parameters on the concentration, temperature, and velocity profiles are provided. Also, the important engineering variables including skin friction, the rate of heat, and mass transfer are examined. The findings suggest that the mass transfer rate declines due to pollutant parameters. Also, the results suggest that the friction factor is uplifted by about 15% and that the heat transfer rate, as well as the mass transfer rate, declines by about 21%, due to the presence of the nanoparticle volume fraction. We believe that these results may improve the flow rate of nanofluid systems, improve heat transfer, and reduce pollutant dispersal. Full article

Fusarium is a genus of fungi found throughout the world. It includes many pathogenic species that produce toxins of agricultural importance. These fungi are also found in buildings and the toxins they spread can be harmful to humans. Distinguishing Fusarium species can be important for selecting effective preventive measures against their spread. A low-cost electronic nose applying six commercially available TGS-series gas sensors from Figaro Inc. was used in our research. Different modes of operation of the electronic nose were applied and compared, namely, gas adsorption and desorption, as well as modulation of the sensor’s heating voltage. Classification models using the random forest technique were applied to differentiate between measured sample categories of four species: F. avenaceum, F. culmorum, F. greaminarum, and F. oxysporum. In our research, it was found that the mode of operation with modulation of the heating voltage had the advantage of collecting data from which features can be extracted, leading to the training of machine learning classification models with better performance compared to cases where the sensor’s response to the change in composition of the measured gas was exploited. The optimization of the data collection time was investigated and led to the conclusion that the response of the sensor at the beginning of the heating voltage modulation provides the most useful information. For sensor operation in the mode of gas desorption/absorption (i.e., modulation of the gas composition), the optimal time of data collection was found to be longer. Full article

Nutshells are regarded as cost-effective and abundant raw materials for producing activated carbons (ACs) for CO₂ capture, storage, and utilization. The effects of carbonization temperature and thermochemical KOH activation conditions on the porous structure as a BET surface, micropore volume, micropore width, and pore size distribution of ACs prepared from walnut (WNS) and hazelnut (HNS) shells were investigated. As a result, one-step carbonization at 900/800 °C and thermochemical KOH activation with a char/KOH mass ratio of 1:2/1:3 were found to be optimal for preparing ACs from WNS/HNS: WNS-AC-3 and HNS-AC-2, respectively. The textural properties of the WNS/HNS chars and ACs were characterized by low-temperature nitrogen vapor adsorption, XRD, and SEM methods. Dubinin’s theory of volume filling of micropores was used to evaluate the microporosity parameters and to calculate the CO₂ adsorption equilibrium over the sub- and supercritical temperatures from 216.4 to 393 K at a pressure up to 10 MPa. The CO₂ capture capacities of WNS- and HNS-derived adsorbents reached 5.9/4.1 and 5.4/3.9 mmol/g at 273/293 K under 0.1 MPa pressure, respectively. A discrepancy between the total and delivery volumetric adsorption capacities of the adsorbents was attributed to the strong binding of CO₂ molecules with the adsorption sites, which were mainly narrow micropores with a high adsorption potential. The high initial differential heats of CO₂ adsorption onto ACs of ~32 kJ/mol confirmed this proposal. The behaviors of thermodynamic functions (enthalpy and entropy) of the adsorption systems were attributed to changes in the state of adsorbed CO₂ molecules determined by a balance between attractive and repulsive CO₂–CO₂ and CO₂–AC interactions during the adsorption process. Thus, the chosen route for preparing ACs from the nutshells made it possible to prepare efficient carbon adsorbents with a relatively high CO₂ adsorption performance due to a substantial volume of micropores with a size in the range of 0.6–0.7 nm. Full article

Adsorption-based carbon dioxide capture, utilization, and storage technologies aim to mitigate the accumulation of anthropogenic greenhouse gases that cause climate change. It is assumed that porous carbons as adsorbents are able to demonstrate the effectiveness of these technologies over a wide range of temperatures and pressures. The present study aimed to investigate the temperature-induced changes in the dimensions of the microporous carbon adsorbent Sorbonorit 4, as well as the carbon dioxide adsorption, by using in situ dilatometry. The nonmonotonic changes in the dimensions of Sorbonorit 4 under vacuum were found with increasing temperature from 213 to 573 K. At T > 300 K, the thermal linear expansion coefficient of Sorbonorit 4 exceeded that of a graphite crystal, reaching 5 × 10⁻⁵ K at 573 K. The CO₂ adsorption onto Sorbonorit 4 gave rise to its contraction at low temperatures and pressures or to its expansion at high temperatures over the entire pressure range. An inversion of the temperature dependence of the adsorption-induced deformation (AID) of Sorbonorit-4 was observed. The AID of Sorbonorit-4 and differential isosteric heat of CO₂ adsorption plotted as a function of carbon dioxide uptake varied within the same intervals of adsorption values, reflecting the changes in the state of adsorbed molecules caused by contributions from adsorbate–adsorbent and adsorbate–adsorbate interactions. A simple model of nanoporous carbon adsorbents as randomly oriented nanocrystallites interconnected by a disordered carbon phase is proposed to represent the adsorption- and temperature-induced deformation of nanocrystallites with the macroscopic deformation of the adsorbent granules. Full article

A series of hybridized charged membrane materials containing carboxyl and silyl groups were prepared via the epoxy ring-opening reaction and sol–gel methods using 3-glycidoxypropyltrimethoxysilane (WD-60) and polyethylene glycol 6000 (PEG-6000) as raw materials and DMF as a solvent. Scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), and thermal gravimetric analyzer/differential scanning calorimetry (TGA/DSC) analysis showed that the heat resistance of the polymerized materials could reach over 300 °C after hybridization. A comparison of the results of heavy metal lead and copper ions’ adsorption tests on the materials at different times, temperatures, pHs, and concentrations showed that the hybridized membrane materials have good adsorption effects on heavy metals and better adsorption effects on lead ions. The maximum capacity obtained from optimized conditions for Cu²⁺ and Pb²⁺ ions were 0.331 and 5.012 mmol/g. The experiments proved that this material is indeed a new environmentally friendly, energy-saving, high-efficiency material. Moreover, their adsorptions for Cu²⁺ and Pb²⁺ ions will be evaluated as a model for the separation and recovery of heavy metal ions from wastewater. Full article

This paper puts forward the use of “low-cost/low-end” hydroxyapatite-based adsorbing materials prepared from Tambaqui fish cleaning residues (i.e., bones) by grinding and/or thermal annealing. The nature of raw materials and treatments practically resulted in a “zero-cost” adsorbent for atrazine pesticide and Co²⁺ ion remediation in an aqueous solution. Despite the distinctive character of the two contaminants, all adsorptions were found to follow pseudo-second order kinetics and Freundlich isotherm models. Pristine hydroxyapatite proved to be more effective in adsorbing atrazine at low concentrations due to interactions with collagen residues. Conversely, heat-treated materials demonstrated better adsorption performances for cobalt due to the removal of organic residues hindering access to the surface. On the other hand, lower adsorption affinities resulted into a faster and more efficient Co²⁺ release into water. The different behavior in terms of phosphate and cobalt release shown by the three hydroxyapatite-based absorbents can be exploited for differential liberation of targeted nutrients, with high seed germination rates. Considering circular economic principles, waste-derived hydroxyapatites may be potentially attractive for removing ionic species, minimizing water pollution stemming from heavy industry, and for their subsequent targeted release to edible plants, enhancing agricultural availability of mineral nutrients for soil fertilization. Full article

Novel hybrid carbon–mineral materials were synthesized by the mechanochemical activation of a mixture of tannin and bentonite in a ball mill with further pyrolysis in an argon atmosphere at 800 °C. The influence of the initial mixture ingredients content on the structural, textural, and thermal characteristics of biochars has been described using X-ray diffraction, Raman and Fourier-transform infrared spectroscopy, nitrogen adsorption–desorption, and scanning electron microscopy. The influence of bentonite clay on the carbon phase characteristics due to the formation of more heat-resistant and structured nanocarbon particles in biochars has been proven. The adsorption effectiveness of the materials towards methylene blue was studied. The adsorption data were analyzed applying Langmuir and Freundlich isotherms with high determination coefficients (R²) in the range of 0.983–0.999 (Langmuir) and 0.783–0.957 (Freundlich). The maximum adsorption amount of MB was 5.78 mg/g. The adsorption efficiency of biochars with respect to phenol was also examined. It was shown that the hybrid biochars show differentiated selectivity to the adsorption of organic compounds. It was concluded that the physicochemical properties of the surface of biochars play an important role in the adsorption effectiveness, making them a good candidate for water and wastewater remediation processes. Full article

In the proposed work, the MATLAB program was used to model and simulate the performance of the investigated two-stage adsorption chiller with and without heat recovery using an activated carbon/methanol pair. The simulated model results were then validated by the experimental results conducted by Millennium Industries. The model was based on 10th order differential equations; six of them were used to predict bed, evaporator and condenser temperatures while the other four equations were used to calculate the adsorption isotherm and adsorption kinetics. The detailed validation is stated in the next paragraphs; for example, it clearly notes that the simulation model results for the two-stage air cooled chiller are well compared with the experimental data in terms of cooling capacity (6.7 kW for the model compared with 6.14 kW from the experimental results at the same conditions). The Coefficient of Performance (COP) predicted by this simulation was 0.4, which is very close to that given by the Carnot cycle working at the same operating conditions. The model optimized the switching time, adsorption/desorption time and heat recovery time to maximize both cooling capacity and COP. The model optimized the adsorption/desorption cycle time (300 to 400 s), switching cycle time (50 s) and heat recovery cycle time (30 s). The temporal history of bed, evaporator and condenser temperatures is provided by this model for both heat recovery and without heat recovery chiller operation modes. The importance of this study is that it will be used as a basis for future series production. Full article