Sorption Isotherms Research Articles

SORPTION OF Fe(III) IONS ON CARBON NITRIDES SYNTHESIED FROM VARIOUS PRECURSORS

In the present work, graphitic carbon nitride powders synthesized from urea, melamine and dicyandiamide were ultrasonic exfoliated and used to evaluate their adsorption efficiency for iron ions –Fe(III) from aqueous solution. It has been established that the efficiency of sorption is significantly influenced by the pH of the medium, contact time, weight of the sorbent and the initial concentration of Fe(III). High adsorption of the iron ion (97–99%) occurs at pH4. It is shown that the Fe(III) sorption isotherm on the studied carbon nitride samples can be modeled by both Langmuir and Freundlich adsorption isotherms based on correlation coefficients

The kinetics of moisture sorption by hair.

The rate process of moisture sorption by human hair has been analysed in order to hints for helping deepen knowledge on the hair structure and to explain the behaviour of hair in response to moisture. The isotherms of moisture sorption by hair were recorded, via dynamic vapour sorption (DVS), for untreated (virgin) and treated (heat-shaped and bleached) hair, as well as for separated cuticle and cortex. By considering that, during moisture uptake, the hair fibres also swell, it is possible to introduce a time-dependent rate constant for describing the kinetics of the moisture sorption. This model allows for clearly separating the moisture sorption processes occurring in Cuticle and in Cortex and for proposing a role of chain entanglement in the two main compartments of the fibre. It may also provide some hints on the structural changes occurring in the fibre after different cosmetic treatments. The influence of the weight of the sample on the kinetics of the sorption process has also been noted and quantified. The analysis pointed to a transition occurring at around 30% relative humidity, assigned to the opening of the hair inner structure, and accommodation of more water molecules. This allowed for an estimate of the value of the activation energy of the water molecules reacting with the active sites, which was found to be in good agreement with results published in the literature. The analysis of the kinetics of moisture sorption by hair was shown not only to provide information on the chain entanglement inside the fibre and the effect of cosmetic treatments but also to demonstrate and quantify the influence of fibre density on the sorption process. It is thus suggested that, along with examination of the hysteresis, the analysis of sorption kinetics helps reveal a more complete picture of hair moisture management.

A new strategy toward synthesis of novel bifunctional N- and S-bearing sorbent for platinum(IV) removal from aqueous solutions and acidic leaching residue of Pt/Al2O3 catalyst

Strong incentive politics have been elaborated for promoting the recovery of precious metals from secondary resources. Solid leaching generates acidic effluents that can be pre-treated using precipitation steps for partial separation before applying sorption for metal recovery from mild acidic solutions. For this purpose, a new sorbent was designed bearing numerous N- and S-bearing reactive groups with good affinity for platinum (as chloroanionic species). Thiazole precursors were first reacted before being grafted (by free radical reaction) with triallyl cyanurate (to form CTTR sorbent). The material was characterized by a series of analytical tools (SEM, BET, FTIR, XPS, TGA, elemental analysis, and titration). The effect of pH combined with FTIR and XPS spectroscopy analyses allowed identifying the mechanisms involved in metal binding: (a) electrostatic attraction of chloroplatinate anions with protonated amine groups (especially in acidic conditions), (b) while at moderate acidic pH metal sorption proceeds through ligand exchange and chelation onto N-based and S-based groups. Optimum sorption was found at pH close to 4 (near pHpzc value). Under selected experimental conditions, the equilibrium was reached in 25–35 min. The pseudo-first order rate equation fitted well experimental profile (though the resistance to intraparticle diffusion contributes to the kinetic control). The maximum sorption capacity at room temperature reached up to 1.58 mmol Pt g−1 (at pH 4). The sorption isotherm was successfully fitted by the Temkin equation. The sorption is spontaneous and exothermic (with reduction in maximum sorption capacity reaching up to 25 %, when temperature increases to 50 °C). Optimum platinum desorption was obtained with 0.3 M HCl solution (with solid/liquid ratio 1.67 g L−1) for complete desorption and enrichment factor close to 4.6. Complete desorption was maintained over 5 cycles, while the sorption efficiency decreased by less than 3.5 % at the fifth cycle. The sorbent showed remarkable stability for PGMs (Pd(II) in addition to Pt(IV)) against alkali-earth elements or base metals (from equimolar synthetic solutions); the selectivity is driven by the preference of the reactive groups (soft base and intermediary base) for soft PGM metals against hard and borderline metal ions; this selectivity is also affected by metal speciation (formation of chloro-anionic species). The valorization of platinum from non-compliant Pt/Al2O3 catalyst was investigated after leaching with aqua regia. Platinum was precipitated from the leachate with ammonium chloride. In a second step, aluminum was removed by precipitation at pH 5. The residual solution was then treated by adsorption on CTTR: optimum separation between Pt and Al was achieved at pH ≈ 3.

Synthesis and Characterization of Mesoporous Materials Functionalized with Phosphinic Acid Ligand and Their Capability to Remove Cd(II).

This article presents a study of cadmium removal from nitrate medium using adsorption in calcined mesoporous silica (MCM-C), mesoporous silica doped (MCM_DIOPA), and calcined and impregnated mesoporous silica (MCM@DIOPA), with diisooctylphosphinic acid (DIOPA). The sorbents were synthesized via a sol-gel method. Several characterization techniques, such as XRD, FTIR spectroscopy, N2 sorption and elemental analysis, have been used to determine the main structural, textural, and chemical properties of prepared sorbents. Batch adsorption and kinetics tests were carried out, where the influence of pH and contact time of the sorbents and their role in cation removal were studied. Experimental results show poor sorption efficiencies with MCM-C and MCM_DIOPA at pH 5.85. At the same pH, better cadmium extraction was attained by MCM@DIOPA and was achieved within 30 min. The pseudo-second-order model is the most appropriate model to describe the elimination mechanism of Cd(II) ions. The Langmuir equation was used to model the sorption isotherm and the maximum sorption capacity of Cd(II) is 22.16 mg/g (200 mmol/kg). The complex type of the probable extracted species isCdL2-HL.

Comprehensive Advanced Physicochemical Characterization and In Vitro Human Cell Culture Assessment of BMS-202: A Novel Inhibitor of Programmed Cell Death Ligand

Background/Objectives: BMS-202, is a potent small molecule with demonstrated antitumor activity. The study aimed to comprehensively characterize the physical and chemical properties of BMS-202 and evaluate its suitability for topical formulation, focusing on uniformity, stability and safety profiles. Methods: A range of analytical techniques were employed to characterize BMS-202. Scanning Electron Microscopy (SEM) was used to assess morphology, Differential Scanning Calorimetry (DSC) provided insights of thermal behavior, and Hot-Stage Microscopy (HSM) corroborated these thermal behaviors. Molecular fingerprinting was conducted using Raman spectroscopy and Fourier Transform Infrared (FTIR) spectroscopy, with chemical uniformity of the batch further validated by mapping through FTIR and Raman microscopies. The residual water content was measured using Karl Fisher Coulometric titration, and vapor sorption isotherms examined moisture uptake across varying relative humidity levels. In vitro safety assessments involved testing with skin epithelial cell lines, such as HaCaT and NHEK, and Transepithelial Electrical Resistance (TEER) to evaluate barrier integrity. Results: SEM revealed a distinctive needle-like morphology, while DSC indicated a sharp melting point at 110.90 ± 0.54 ℃ with a high enthalpy of 84.41 ± 0.38 J/g. HSM confirmed the crystalline-to-amorphous transition at the melting point. Raman and FTIR spectroscopy, alongside chemical imaging, confirmed chemical uniformity as well as validated the batch consistency. A residual water content of 2.76 ± 1.37 % (w/w) and minimal moisture uptake across relative humidity levels demonstrated its low hygroscopicity and suitability for topical formulations. Cytotoxicity testing showed dose-dependent reduction in skin epithelial cell viability at high concentrations (100 µM and 500 µM), with lower doses (0.1 µM to 10 µM) demonstrating acceptable safety. TEER studies indicated that BMS-202 does not disrupt the HaCaT cell barrier function. Conclusions: The findings from this study establish that BMS-202 has promising physicochemical and in vitro characteristics at therapeutic concentrations for topical applications, providing a foundation for future formulation development focused on skin-related cancers or localized immune modulation.

Development and characterization of “Greek Salad” edible films

“Greek salad” edible films, made from tomato puree, juices of cucumber, bell pepper and onion, oregano oil and apple pectin with and without olive oil and guar gum were successfully prepared and characterized for water vapor permeability, oxygen permeability, tensile properties, moisture sorption isotherm, heat sealing ability and color. It was found that the addition of olive oil to the basic film increased its water vapor permeability, while the incorporation of guar gum had no impact on it. The addition of olive oil and guar gum affected the tensile properties, the isotherms for moisture sorption and the color of the films. All films demonstrated good heat-sealing properties. The FTIR spectra of the films displayed several interesting characteristics, confirming the films’ composition. The sensory evaluation of the four edible films revealed that all samples scored close to or above 3 (on a scale of 0–5) in most sensory attributes, indicating general acceptability among panelists. Notably, films containing guar gum exhibited higher homogeneity and transparency, while films containing olive oil showed the highest odor, flavor, and taste intensities, but also more pronounced defects and undesirable aftertastes. The basic film appeared more balanced in most sensory attributes.It was concluded that overall the advantages of adding olive oil and guar gum to the basic film were not significant. Future experiments will concentrate on optimizing the production of the basic film and exploring the possibility of using it for packaging oily foods.

Vacancy Effect on the Luminescent and Water Responsive Properties of Vacancy-Ordered Double Perovskite Derivatives.

Vacancy-ordered perovskites and derivatives represent an important subclass of hybrid metal halides with promise in applications including light emitting devices and photovoltaics. Understanding the vacancy-property relationship is crucial for designing related task-specific materials, yet research in this field remains sporadic. For the first time, we use the Connolly surface to quantitatively calculate the volume of vacancy (V□, □=vacancy) in vacancy-ordered double perovskite derivatives (VDPDs). A relationship between void fraction and the structure, photoluminescent properties and humidity stability was established based on zero-dimensional (0-D) [N(alkyl)4]2Sb□Cl5□'-type VDPDs. Compared with the more commonly studied A2M(IV)X6□-type double perovskite (A=cation, M=metal ion, X=halide), [N(alkyl)4]2Sb□Cl5□' features double vacancy sites. Our results demonstrate an inverse relationship between the photoluminescent quantum yield and V□ in 0-D VDPDs. Additionally, structural transformation from A2SbCl5 to A3Sb2Cl9 was first reported, during which the novel 'gate-opening' gas adsorption phenomenon was observed in VDPDs for the first time, as evidenced by 'S'-shaped sorption isotherms for water vapor, indicating a cation-controlled water-vapor response behavior. A mixed-cation strategy was developed to modulate the humidity stability of VDPDs. Characterized by controllable water-responsive behavior and unique 'on-off-on' luminescent switching, A2M(III)□X5□'-type materials show great promise for multi-level information anti-counterfeiting applications.

Vacancy Effect on the Luminescent and Water Responsive Properties of Vacancy‐Ordered Double Perovskite Derivatives

AbstractVacancy‐ordered perovskites and derivatives represent an important subclass of hybrid metal halides with promise in applications including light emitting devices and photovoltaics. Understanding the vacancy‐property relationship is crucial for designing related task‐specific materials, yet research in this field remains sporadic. For the first time, we use the Connolly surface to quantitatively calculate the volume of vacancy (V□, □=vacancy) in vacancy‐ordered double perovskite derivatives (VDPDs). A relationship between void fraction and the structure, photoluminescent properties and humidity stability was established based on zero‐dimensional (0‐D) [N(alkyl)4]2Sb□Cl5□′‐type VDPDs. Compared with the more commonly studied A2M(IV)X6□‐type double perovskite (A=cation, M=metal ion, X=halide), [N(alkyl)4]2Sb□Cl5□′ features double vacancy sites. Our results demonstrate an inverse relationship between the photoluminescent quantum yield and V□ in 0‐D VDPDs. Additionally, structural transformation from A2SbCl5 to A3Sb2Cl9 was first reported, during which the novel ‘gate‐opening’ gas adsorption phenomenon was observed in VDPDs for the first time, as evidenced by ‘S’‐shaped sorption isotherms for water vapor, indicating a cation‐controlled water‐vapor response behavior. A mixed‐cation strategy was developed to modulate the humidity stability of VDPDs. Characterized by controllable water‐responsive behavior and unique ‘on‐off‐on’ luminescent switching, A2M(III)□X5□′‐type materials show great promise for multi‐level information anti‐counterfeiting applications.

Caffeine removal from water using rice husk residue biochar: characterization, kinetics and sorption isotherms

Caffeine removal from water using rice husk residue biochar: characterization, kinetics and sorption isotherms

Metamaterial-based radar-infrared camouflage material for building insulation: Design and performance analysis

This study introduces a metamaterial microwave absorber (MMA)-lightweight envelope (LE), which is an innovative solution for integrating electromagnetic and infrared-compatible camouflage technologies into building structures. Specifically, MMA-LE incorporates a MMA into building designs for microwave/infrared-compatible camouflage. This study evaluated the microwave absorption performance, infrared camouflage capabilities, and energy-saving effects of MMA-LEs by analyzing the microwave absorption characteristics using the impedance matching theory and simulation software. A coupled heat and moisture transfer model was used to assess isothermal moisture absorption, heat transfer coefficients, and annual heating/cooling loads. Furthermore, infrared imaging tests verified the effectiveness of the camouflage. Two MMA-LE designs (single and double absorber layers) achieve over 90 % microwave absorption in the 3.2–11.2 GHz and 1.85–12.67 GHz frequency ranges with relative bandwidths of 111.1 % and 149 %, respectively, and with polarization insensitivity. Moreover, the MMA-LE enhanced the wall heat and moisture transfer performance, reduced the relative humidity, and reduced the thermal load under Guangzhou's climate conditions. However, despite the improved moisture resistance, the double-layer MMA-LE increased the envelope moisture content, thus reducing thermal insulation. In addition, the limited absorbency of the substrate material results in a modest increase in the dielectric constant, consequently decreasing the resonant frequency of the hybrid structure compared to dry samples. Nevertheless, the thermal insulation properties of MMA-LEs effectively insulate the internal heat sources, achieving optimal infrared camouflage. In conclusion, this study provides a novel solution for microwave-infrared-compatible camouflage in building applications, offering significant theoretical and practical value.

Dynamic pH‐Responsive Release and Biological Impact of In‐Situ Quercetin‐Modified MIL‐101(Fe)‐NH2

A successful investigation was conducted on the in‐situ modification of MIL‐101(Fe)‐NH2 with quercetin and its controlled release under various pH conditions. MIL‐101(Fe)‐NH2 was synthesized using an electrochemical method at room temperature (15 volts, 30 minutes). The formation of the material was confirmed through comprehensive analyses, including PXRD, FTIR, and TGA. Nitrogen sorption isotherm measurements revealed that Qu@MIL‐101(Fe)‐NH2 exhibited a smaller surface area compared to MIL‐101(Fe)‐NH2, with both materials classified as mesoporous. Transmission electron microscopy (TEM) clearly depicted the materials' octahedral microspindle morphology. The cumulative percent release (CPR) of quercetin from Qu@MIL‐101(Fe)‐NH2 over 72 hours was determined to be 53.45% at pH 1.2, 19.48% at pH 4.8, and 5.87% at pH 7.4. Notably, quercetin release in the acidic microenvironment representative of cancer cells (pH 4.8) was nearly four times higher than under physiological conditions (pH 7.4). Kinetic release studies indicated that quercetin release from Qu@MIL‐101(Fe)‐NH2 followed the Ritger‐Peppas kinetic model, suggesting non‐Fickian diffusion. The MIL‐101(Fe)‐NH2 nanocarriers, with in‐situ‐loaded quercetin, demonstrated promising potential for pH‐triggered drug release. Additionally, the safety of MIL‐101(Fe)‐NH2 in biological models and the anticancer efficacy of quercetin were evaluated in vitro using two liver cancer cell lines.

Vitamin B Complex Encapsulation in Bacterial Nanocellulose: A Novel System for Heat and Chemical Stabilization in Food Products.

Bacterial nanocellulose has been commonly used as a gelling or stabilizing agent in the food industry and as an excipient in pharmacology. However, due to its physical and chemical properties, such as its high degradation temperature and the ease with which it can interact with other molecules, bacterial nanocellulose has been established as a material with great potential for the protection of bioactive compounds. This research shows the capacity of bacterial nanocellulose to establish interactions with B vitamins (B1, B2, B3 and B12) through different sorption isotherms, mainly by means of the BET, GAB and TSS models. First, the degradation of the vitamin B complex, which mostly occurs upon heating, is minimized in the presence of BNC, herein proposed as a thermal stabilizer. Secondly, BNC is shown to bind to micronutrients and act as dietary fiber. BNC acts as a thickening and water-binding agent. The effects of BNC are determined to occur as an encapsulation system that facilitates affinity adsorption in mono- and multilayers. Finally, bacterial nanocellulose was used as an encapsulating agent for the vitamin B complex by spray drying. It is demonstrated that BNC is a very successful new nanomaterial for encapsulation, with a high level of adsorption, and for the protection of hydro-soluble vitamins. BNC has shown great potential to adsorb vitamins B1, B2, B3 and B12 owing to their hydroxyl groups, which are responsible for its water or vitamin sorption. Due to the features of bacterial nanocellulose, it is possible to use it as a raw material in the food industry to protect micronutrients during the thermal process.

Ultrafast and Highly Selective Sequestration of Radioactive Barium Ions by a Layered Thiostannate.

As a simulant of hazardous 226Ra2+, the simultaneously selective and rapid elimination of radioactive 133Ba2+ ions from geothermal water is necessary but still challenging. In this paper, we demonstrated the usability of a layered thiostannate with facile synthesis and inexpensive cost, namely, K2xSn4-xS8-x (KTS-3, x = 0.65-1), for the remediation of radioactive 133Ba2+ in multiple conditions, including sorption isotherm, kinetics, and the influences of competitive inorganic/organic ions, pH values, and dosages. KTS-3 has a strong barium uptake ability (171.3 mg/g) and an ultrafast adsorption kinetics (about 2 min). Impressively, it can achieve a high preference for barium regardless of the excessive interference ions (Na+, K+, Mg2+, Ca2+, and humic acid) and acidic/alkaline environments, with the largest distribution coefficient Kd value reaching 6.89 × 105 mL/g. Also, the Ba2+-laden products can be easily eluted by a concentrated KCl solution, and its adsorption performances for barium resist well even after five consecutive cycles. In addition, owing to the regular appearance and excellent mechanical strength, the prepared KTS-3/PAN (PAN = polyacrylonitrile) granule displays a good removal efficiency in the flowing ion-exchange column. These advantages mentioned above render it very promising for the effective and efficient cleanup of radioactive 133Ba2+-contaminated wastewater.

Modelling of water sorption hysteresis of cement-based materials based on pore microstructure

This paper presents a model for predicting water sorption isotherms of cement-based materials. In this model, hysteresis contributions of interlayer pores and gel/capillary pores are calculated separately. The hysteresis model of gel/capillary pores is achieved in four steps: (i) quantification of the pore network, (ii) determination of the criterion of saturation/desaturation of pores, (iii) derivation of the two-dimensional volumetric density distribution function, (iv) calculation of the real-time water content of gel/capillary pores. The hysteresis of interlayer pores is represented by an empirical model based on experiments. The reliability of the model is verified by comparing the model predictions and the experimental data in the literatures. Furthermore, three subjects were discussed: the influence of pore network on hysteresis, the hysteretic behavior of water in pores, the interaction of hysteresis mechanisms.

Evaluating the environmental and agronomic implications of bone char and biochar applications to loamy sand based on sorption data

BackgroundThe widely adopted use of charred biomass for agronomic and environmental purposes; and the reported positive and deleterious effects necessitated the need for this study to ascertain the potential causes of the erratic results surrounding the use of charred biomass in agriculture and the environment. A batch sorption experiment was carried out to determine the sorptive and desorptive capacity of bone char and biochar on nitrate, ammonium, phosphate and sulphate concentrations in a loamy sand soil. The potential agronomic and environmental implications of the sorption data were also discussed.ResultsThe results indicated that bone char is richer in nutrient composition than biochar, with 70% more ability to sorb nutrients. The bone char and biochar sorption isotherms conformed to the H-curve isotherm type. Bone char and biochar have multiple layers of adsorption sites. Nutrient adsorption maxima, binding energy, and maximum buffering capacities of the soil were increased with the addition of bone char and biochar. The unamended soil was observed to retain as low as 6% of added nitrate to as much as 58% of added phosphate, while bone char retained 56% of added sulphate, 47% of phosphate, 76% nitrate and 64% of ammonium. Generally, bone char retained 60.6% of the added nutrients, while biochar retained 40.7% of the nutrients. The addition of bone char led to a 45.8% increase in the nutrient retention ability of the soil and a 36.1% increase with the addition of biochar.ConclusionThe nutrient sorption characteristics of biochar should be studied prior to its use as a soil nutrient amendment. It was concluded that bone char or biochar is a potential soil nutrient immobilizer; hence, applications for agronomic purposes should take cognizance of the native soil fertility so as to appropriately add fertilizer input before use.

Structure–property relationships and nanofiller‐induced hydro‐anti‐plasticization in polyhydroxyurethane/POSS hybrid composites

AbstractNon‐isocyanate polyhydroxyurethanes/polyhedral oligomeric silsesquioxane (PHU/POSS) hybrid composites are prepared by in situ physical introduction of octa(3‐hydroxy‐3‐ethylbutyldimethylsiloxy) POSS into a linear non‐isocyanate polyhydroxyurethane matrix. The amorphous nature of the matrix is retained in the composites and no POSS crystals are observed. Thermal and mechanical properties are studied along with water‐polymer interactions and are discussed in terms of structure‐properties relationships. POSS has only minimal effect on thermal stability. Composite materials with up to 2 wt% POSS exhibit an increased rubbery modulus. The glass transition temperature of the composite materials increases up to 2 wt% loading and decreases at higher POSS content. Water‐polymer interactions are studied in a broad range of relative humidity (0–0.97). Materials exhibit a relatively high water absorption, which is enhanced by POSS at low concentrations. Moisture sorption isotherms are discussed in terms of the Guggenheim‐Anderson‐de Boer model. The study of molecular mobility of hydrated systems by differential scanning calorimetry reveals a peculiar POSS‐induced antiplasticization in PHU/POSS blends at 10–20 wt% water uptake, possibly due to the formation of POSS‐centered water clusters.

In situ growth of ZIF-8 on cellulose microspheres with high doxorubicin loading capacity and pH-sensitive for oral drug delivery

Metal-organic framework (MOF) nanoparticles are a class of porous nanomaterials with wide application prospects. Zeolitic imidazolate framework (ZIF) materials have high loading performance and pH-sensitive characteristics, which means they have great development prospects in the development of drug carrier systems. Herein, cellulose microspheres (CM) were used as a carrier for the nucleation and growth of ZIF-8 nanocrystals. CM@ZIF-8 was prepared in situ, which was more convenient, flexible, cost-effective, and highly safe. CM@ZIF-8, as a novel carrier, was used to monitor the release of the anticancer drug Doxorubicin (DOX) and prevent it from dissipating before reaching its goal. The designed DOX-loaded CM@ZIF-8 (CM@ZIF-8-DOX) system was characterized by FTIR, SEM, N2 sorption isotherm, XRD, and Cytotoxicity assay (cells survival rate 95.08 %). CM@ZIF-8-DOX exhibited controlled drug release behavior in simulated in-vitro tumor microenvironments (81.2 % drug release throughout 72h). CM@ZIF-8 simultaneously had a high loading capacity of DOX (Qe = 159.71 mg∙g−1), and the amount released under acidic conditions (pH 5.0) was greater (63.4 % after 15 h) than under neutral conditions (pH 7.4) due to the detachment of the coordination between metal ions and ligands (37.6 % after 15 h).

Effects of Humidity on Mycelium-Based Leather.

Leather is a product that has been used for millennia. While it is a natural material, its production raises serious environmental and ethical concerns. To mitigate those, the engineering of sustainable biobased leather substitutes has become a trend over the past few years. Among the biobased materials, mycelium, the fungal "root" of a mushroom, is one of the promising alternatives to animal leather, as a material with tunable physicomechanical properties. Understanding the effect of humidity on mycelium-based leather material properties is essential to the production of durable, competitive, and sustainable leather products. To this end, we measured the water sorption isotherms on several samples of mycelium-based leather materials and investigated the effects of water sorption on their elastic properties. The ultrasonic pulse transmission method was used to measure the wave speed through the materials while measuring their sorption isotherms at different humidity levels. Additionally, the material's properties were mechanically tested by performing uniaxial tensile tests under ambient and immersed conditions. An overall reduction in elastic moduli was observed during both absorption and immersion. The changes in the measured longitudinal modulus during water sorption reveal changes in the elasticity of the test materials. The observed irreversible variation of the longitudinal modulus during the initial water sorption can be related to the material production process and the presence of various additives that affect the mechanical properties of the leather materials. Our results presented here should be of interest to material science experts developing a new generation of sustainable leather products.

Determination of Moisture Sorption Isotherm using Brunauer-Emmett-Teller (BET) and Guggenheim-Anderson-de Boer (GAB) Models, Germination Capacity and Index Vigor of Soybean during Storage

Understanding the interaction between the equilibrium moisture content of a product and the surrounding air is crucial for guaranteeing product quality and preserving its characteristics throughout storage. The study of this tendency may be conducted utilizing sorption isotherms. This research aimed to study the moisture sorption characteristics of soybeans during storage, identify the most suitable mathematical model for the experimental data, and examine the relationship between the germination capacity and vigor index of soybeans with their moisture content and water activity. Moisture sorption characteristics of soybean, Anjasmara variety, were investigated at temperatures of 30ᵒC, 40ᵒC, and 50ᵒC, and water activities of 0.08 to 0.80, and were modelled using two different mathematical models, Brunauer-Emmett-Teller (BET) and Guggenheim-Anderson-de Boer (GAB). Both two mathematical models, BET and GAB, were found to effectively describe the moisture sorption data based on regression analyses and goodness of fit. Each model was statistically evaluated by coefficient of determination and deviation standard. The moisture sorption behaviour of soybean seeds displayed a sigmoidal pattern. The GAB models have been suggested to estimate the moisture content at certain humidity levels at 30ᵒC, 40ᵒC, and 50ᵒC temperatures. The BET models were suitable for temperatures between 30ᵒC and 40oC. The vigor and germination indicated exhibited a progressive and optimal trend at a water activity level of 0.32, followed by a decline at all three temperatures.

Drying Kinetics and Sorption Isotherms of Biocomposite Materials: Experimental Investigation and Modeling Analysis.

Modern materials science has made significant progress in creating new materials and processes for waste recovery. One such advancement involves the development of a new porous composite material made from clay and an environmentally sustainable eggshell powder. In this study, the dynamic behavior of water vapor during desorption and adsorption processes within this composite material was investigated. The moisture diffusivity coefficient was determined within the clay/eggshell powder composite material. The drying kinetic data were analyzed using various models such as Newton, Page, and Wan and Singh. The static gravimetric vapor adsorption/desorption experiments were conducted at different temperatures (30, 40, 50, 60, and 70 °C) to depict the material's capacity for absorbing and releasing moisture over time. The experimental isotherm data were fitted using different mathematical models (Guggenheim, Anderson, and De Boer, Peleg, Adam and Shove, Oswin, and Modified Henderson). The findings suggest that integrating eggshell powder with clay can significantly influence the behavior and characteristics of the resultant material. The combination of eggshell powder and clay reduces moisture sorption and accelerates the drying process. Consequently, this affects the porosity, permeability, and response to humidity changes.