Dehydration Temperature Research Articles

Maximizing methane production in adsorptive nitrogen removal from natural gas: The impact of dehydration temperature on Ba-ETS-4 separation performance

Ba-ETS-4 is a promising adsorbent for nitrogen removal from low-grade natural gas. However, the Ba-ETS-4 adsorption characteristics, i.e., both adsorption kinetics and equilibrium capacity, change by dehydration temperature owing to structural shrinkage and pore contraction which finally impact the separation performance of the adsorption bed. In this paper, experimental breakthrough data are provided for N2/CH4 separation at various Ba-ETS-4 dehydration temperatures (250°C-450 °C) followed by a separation performance analysis in generating methane as the main product. Additionally, isotherm data at different temperatures (20 °C, 40 °C, 60 °C and 80 °C) are presented for selected dehydration temperatures (250 °C, 350 °C, 400 °C and 440 °C). The results revealed that an increase in dehydration temperature leads to a decrease in adsorption capacity but a better separation by providing more hindrance for CH4 diffusion, while not affecting the N2 breakthrough wavefront. At a dehydration temperature of 250 °C, the N2 breakthrough time is the highest, indicating the ability to process a larger feed. However, this also leads to the least CH4 production (0.037 mmol/g), as most of the fed CH4 is adsorbed onto the bed. Interestingly, an increase in dehydration temperature leads to an increase in CH4 production up to 420 °C (0.140 mmol/g), after which the CH4 production decreases sharply.

Effect of evaporation temperature on evaporative residue properties of waterborne polyurethane modified emulsified asphalt

Abstract In recent years, waterborne polyurethane (WPU) modified emulsified asphalt has attracted much attention. The conventional property of WPU-modified emulsified asphalt (WPU-MEA) is usually measured by using the evaporative residue obtained at high temperatures. In this work, WPU-MEA was prepared and the influence of evaporative temperature on the conventional performances (softening point, penetration, ductility) of the residue of WPU-MEA was investigated. Fourier Transform Infrared Spectroscopy (FTIR) and Fluorescence microscope (FM) were used to analyze the chemical structure and morphology of the evaporative residues. It was found that the evaporation dehydration temperature has a significant influence on the property of the evaporation residue of WPU-MEA. The evaporative residue performance of WPU modified asphalt was better at an evaporation temperature of 110°C, and the three conventional properties were significantly improved. Upon increasing the evaporation temperature, the conventional properties of WPU-MEA continue to decrease. As the evaporation temperature is 190°C, the conventional property of the residue is close to that of unmodified emulsified asphalt. Considering the performance index of WPU-MEA, the optimal evaporation temperature should be determined in the characterization of residue performance. This study has a guiding significance for the development of polyurethane-modified asphalt materials.

Tutton salt (NH4)2Zn(SO4)2(H2O)6: thermostructural, spectroscopic, Hirshfeld surface, and DFT investigations

ContextAmmonium Tutton salts have been widely studied in recent years due to their thermostructural properties, which make them promising compounds for application in thermochemical energy storage devices. In this work, a detailed experimental study of the Tutton salt with the formula (NH4)2Zn(SO4)2(H2O)6 is carried out. Its structural, vibrational, and thermal properties are analyzed and discussed. Powder X-ray diffraction (PXRD) studies confirm that the compound crystallizes in a structure of a Tutton salt, with monoclinic symmetry and P21/a space group. The Hirshfeld surface analysis results indicate that the main contacts stabilizing the material crystal lattice are H···O/O···H, H···H, and O···O. In addition, a typical behavior of an insulating material is confirmed based on the electronic bandgap calculated from the band structure and experimental absorption coefficient. The Raman and infrared spectra calculated using DFT are in a good agreement with the respective experimental spectroscopic results. Thermal analysis in the range from 300 to 773 K reveals one exothermic and several endothermic events that are investigated using PXRD measurements as a function of temperature. With increasing temperature, two new structural phases are identified, one of which is resolved using the Le Bail method. Our findings suggest that the salt (NH4)2Zn(SO4)2(H2O)6 is a promising thermochemical material suitable for the development of heat storage systems, due to its low dehydration temperature (≈ 330 K), high enthalpy of dehydration (122.43 kJ/mol of H2O), and hydration after 24 h.MethodsComputational studies using Hirshfeld surfaces and void analysis are conducted to identify and quantify the intermolecular contacts occurring in the crystal structure. Furthermore, geometry optimization calculations are performed based on density functional theory (DFT) using the PBE functional and norm-conserving pseudopotentials implemented in the Cambridge Serial Total Energy Package (CASTEP). The primitive unit cell optimization was conducted using the Broyden–Fletcher–Goldfarb–Shanno (BFGS) algorithm. The electronic properties of band structure and density of states, and vibrational modes of the optimized crystal lattice are calculated and analyzed.Graphical abstract

Exploring the Diversity and Dehydration Performance of New Mixed Tutton Salts (K2V1−xM’x(SO4)2(H2O)6, Where M’ = Co, Ni, Cu, and Zn) as Thermochemical Heat Storage Materials

Tutton salts form an isomorphic crystallographic family that has been intensively investigated in recent decades due to their attractive thermal and optical properties. In this work, we report four mixed Tutton crystals (obtained by the slow solvent evaporation method) with novel chemical compositions based on K2V1−xM’x(SO4)2(H2O)6, where M’ represents Co, Ni, Cu, and Zn, aiming at thermochemical energy storage applications. Their structural and thermal properties were correlated with theoretical studies. The crystal structures were solved by powder X-ray diffraction using the Rietveld method with similar compounds. All of the samples crystallized in monoclinic symmetry with the P21/a-space group. A detailed study of the intermolecular interactions based on Hirshfeld surfaces and 2D fingerprint mappings showed that the main interactions arise from hydrogen bonds (H∙∙∙O/O∙∙∙H) and dipole–ion (K∙∙∙O/O∙∙∙K). On the other hand, free space percentages in the unit cells determined by electron density isosurfaces presented low values ranging from 0.53 (V–Ni) to 0.81% (V–Cu). The thermochemical findings from thermogravimetry, a differential thermal analysis, and differential scanning calorimetry indicate that K2V0.47Ni0.53(SO4)2(H2O)6 salt is the most promising among mixed salts (K2V1−xM’x(SO4)2(H2O)6) for heat storage potential, achieving a low dehydration temperature (≈85 °C), high dehydration enthalpy (≈360 kJ/mol), and high energy storage density (≈1.84 GJ/m3).

Postharvest dehydration of red grapes: impact of temperature and water-loss conditions on free and glycosylated volatile metabolites of exocarp and epicarp of Nebbiolo and Aleatico varieties.

Postharvest dehydration affects the metabolism of grapes, impacting odorous secondary metabolites and therefore the features of the corresponding passito wines - high-quality products with winemaking practices linked to specific territories and related autochthonous grape varieties. Water loss and temperature conditions are the main variables of the dehydration process. This study assessed how they impacted the patterns of free and glycosylated volatile organic compounds (VOCs) of the exocarp (pulp) and epicarp (skin) in Nebbiolo and Aleatico, a neutral and semi-aromatic red grape variety, respectively. Dehydration parameters were set in tunnel conditions, and VOCs were quantitatively analyzed by solid phase extraction-gas chromatography-mass spectrometry. For Nebbiolo grapes, weight loss had a greater impact on free volatiles than dehydration temperature, with a 20% weight loss increasing total VOCs in both exocarp and epicarp. Low temperature (10 °C) significantly increased (P < 0.05) the glycosylated VOCs' terpene content. In Aleatico grapes, weight loss was key in modulating free volatiles, with 30% weight loss and 15 °C leading to significant increases in VOCs, especially exocarp terpenes, acids and benzenoids. More stressful dehydration (30% weight loss at 25 °C) resulted in higher aroma precursor concentrations. These findings can assist passito wine production in preserving varietal aromas of original grapes trough optimized dehydration conditions, preventing sensory homologation occurring because of strong uncontrolled dehydration. They can also promote optimization of energy consumption, thus fostering financial and environmental sustainability. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Fe/LiNO3/TiN co–modified MgO for enhanced thermochemical energy storage performance in MgO/Mg(OH)2 cycles

MgO/Mg(OH)2 thermochemical energy storage can convert solar energy and industrial waste heat into forms that are easier to store and transport by cyclic hydration/dehydration reactions. To achieve excellent energy storage performance, cyclic stability and optical absorption capability of MgO/Mg(OH)2, Fe/LiNO3/TiN co–modified MgO were synthesized for energy storage cycles by wet-mixing method. The energy storage performance, cyclic stability and dehydration kinetics of Fe/LiNO3/TiN co–modified MgO were studied in dual fixed–bed system and simultaneous thermal analyzer. The experimental results show that the Fe and LiNO3 in the composite not only increase the hydration conversion of MgO by 6.3 times at 30 min, but also reduce the dehydration temperature and dehydration activation energy of Mg(OH)2 by 99.4 °C and 64 %, respectively. TiN overcomes aggregation of MgO and sustains the excellent porous structure, which results in only a 9 % decrease in energy storage performance of Fe/LiNO3/TiN co–modified MgO after 15 energy storage cycles. Subsequently, TiN significantly strengthens the optical absorption performance of Mg(OH)2 and photothermal temperature under xenon-lamp simulated sunlight radiation. Furthermore, density functional theory calculation reveals that Fe and Li enhance the adsorption of H2O on MgO model and reduce energy barrier for hydration reactions by 62.76 %, while TiN effectively inhibits MgO clusters migration within the material and enhances the optical absorption coefficient. Hence, Fe/LiNO3/TiN co–modified MgO shows significant research value in MgO/Mg(OH)2 energy storage process.

Carbon Fibers Based on Cellulose–Lignin Hybrid Filaments: Role of Dehydration Catalyst, Temperature, and Tension during Continuous Stabilization and Carbonization

Lignocellulose has served as precursor material for carbon fibers (CFs) before fossil-based polymers were discovered as superior feedstock. To date, CFs made from polyacrylonitrile have dominated the market. In search of low-cost carbon fibers for applications with medium strength requirements, cellulose and lignin, either as individual macromolecule or in combination, have re-gained interest as renewable raw material. In this study, cellulose with 30 wt% lignin was dry-jet wet-spun into a precursor filament for bio-based carbon fibers. The stabilization and carbonization conditions were first tested offline, using stationary ovens. Diammonium sulfate (DAS) and diammonium hydrogen phosphate were tested as catalysts to enhance the stabilization process. Stabilization is critical as the filaments’ strength properties drop in this phase before they rise again at higher temperatures. DAS was identified as a better option and used for subsequent trials on a continuous carbonization line. Carbon fibers with ca. 700 MPa tensile strength and 60–70 GPa tensile modulus were obtained at 1500 °C. Upon further carbonization at 1950 °C, moduli of &gt;100 GPa were achieved.

Dehydration of goethite during vacuum step-heating and implications for he retentivity characterization

Uncertainty exists over what environmental conditions and mineralogical/chemical properties are required to ensure retention of helium such that (UTh)/He dates record the time of goethite crystallization. We undertook vacuum step heating experiments to determine He diffusion parameters for extrapolation to Earth surface conditions on 10 goethite specimens in which we had created a uniform distribution of 3He. Arrhenius plots of apparent diffusion coefficients on all samples follow the same pattern. At temperatures <200 °C the data define arrays consistent with progressive degassing of increasingly large crystallites. However, above 200 °C the computed diffusivities increase dramatically until about 80% of the helium is extracted, after which they suddenly decline. The sudden increase in diffusivity at 200 °C coincides with the onset of dehydration of the goethite structure, a process which continues throughout the remainder of the step heat. There is a strong correlation between evolved water and 3He amounts. These observations likely reflect previously reported processes of formation, growth, and coalescence of pores as the phase transition to hematite proceeds. While significantly higher dehydration temperatures of ∼270 °C are observed using techniques such as thermogravimetric analysis in air, the long step durations, and vacuum conditions of our experiments destabilize goethite. Orders of magnitude differences in the computed diffusivities among our samples may reflect crystallite-size-distribution control on dehydration kinetics, and the qualitative size distributions we infer from the step heats are consistent with SEM observations of crystallite lengths. Vacuum step-heating experiments in which goethite is decomposing cannot be used to determine He diffusion behavior in nature, but the inferred crystallite size distribution provides some useful indirect evidence. A strong relationship exists between metrics of the crystallite size distribution from step heating results and the degree of He retention in nature inferred from the 4He/3He method. This observation provides evidence supporting the validity of the 4He/3He technique for estimating retention, and further suggests that the dominant control on He retention in nature is the crystallite size distribution. Experiments under hydrothermal conditions in which goethite remains stable may be an alternative approach to address the question of He diffusion behavior in nature.

Dehydration behaviors and properties of anhydrite II prepared by phosphogypsum with low-temperature calcination

Certain concentration H+ can combine with the crystal water to form the H3O+, influencing the stability of the crystal water in dihydrate so that can be completely removed under lower temperature. Therefore, this paper introduces a method wherein sulfuric acid is employed as a medium, facilitating direct dry mixing and low calcination temperatures to produce anhydrite II. Initially, the low and high calcination temperatures were determined as 280°C and 500°C, respectively, through XRD analysis of the phase composition of calcination products under varying conditions. Subsequently, the influence of different sulfuric acid contents and concentrations on the calcination products at 280°C was investigated. Additionally, the impact of sulfuric acid on the dehydration behavior of PG was analyzed using TG-DSC and FTIR. The present work also assessed the physical-mechanical properties of anhydrite II at 280°C and 500°C, along with their hydration activity and microscopic morphology. The results indicated that the optimal sulfuric acid content and concentration were determined as 2 % and 40 wt%, respectively, yielding dehydration temperatures of 86.08°C and 146.95°C. The water requirement (WR) for normal consistency for anhydrite II at 280°C was 0.68, exhibiting higher flexural and compressive strength compared to calcination at 500°C (WR=0.58), and the hydration rate at 28 days reached 78.5 %. At 280°C, the dihydrate crystals formed by anhydrite II at 28 days exhibited a compact microstructure characterized by relatively small crystals with well overlapping.

Convective drying of bitter yam slices (Dioscorea bulbifera): Mass transfer dynamics, color kinetics, and understanding the microscopic microstructure through MATLAB image processing

The objective of this research endeavor was to enhance the quality and storability of Dioscorea bulbifera through the investigation of the effects of pre-treatment (soaking) and different dehydration temperatures (50, 60, and 70°C) on its mass transfer, color kinetics, texture, microstructure, and rehydration properties. Ten drying and four-color kinetics models were employed to describe drying behavior and color changes. The drying process demonstrated a falling rate, with reduced drying time (from 960 to 540 min) as the convective temperature increased from 50 to 70°C. Moisture diffusivity increased with increasing hot air temperatures (4.15 ×10–10 – 1.03 ×10–9 m2/s), and the activation energy was determined as 41.82 kJ/mol. Slices dried at 70 °C exhibited higher color change than those dried at 50°C. The modified color model fitted the best color parameters, followed by the fraction model. Slices dried at 60°C showed lower hardness (34.73 N) and higher porosity (27.03 %) as compared with 50°C (49.33 N and 19.82 %) and 70°C (40.16 N and 21.90 %) temperature. Microstructure, moisture diffusion, and texture were closely linked to temperature and moisture content. Boiling and potassium metabisulfite significantly affected drying rate and texture of yam slices . MATLAB analysis provided detailed pore information for each hot air-dried sample, correlating with texture characteristics. This research offers substantial industrial significance by providing methods to enhance dried yam products' quality, shelf-life enhancement, and further exploration of starch extraction and recovery of valuable bioactive compounds.

Efficient Determination of Critical Water Activity and Classification of Hydrate-Anhydrate Stability Relationship

For a pair of hydrated and anhydrous crystals, the hydrate is more stable than the anhydrate when the water activity is above the critical water activity (awc). Conventional methods to determine awc are based on either hydrate-anhydrate competitive slurries at different aw or solubilities measured at different temperatures. However, these methods are typically resource-intensive and time-consuming. Here, we present simple and complementary solution- and solid-based methods and illustrate them using carbamazepine and theophylline. In the solution-based method, awc can be predicted using intrinsic dissolution rate (IDR) ratio or solubility ratio of the hydrate-anhydrate pair measured at a known water activity. In the solid-based method, awc is predicted as a function of temperature from the dehydration temperature and enthalpy obtained by differential scanning calorimetry (DSC) near a water activity of unity. For carbamazepine and theophylline, the methods yielded awc values in good agreement with those from the conventional methods. By incorporating awc as an additional variable, the hydrate-anhydrate relationship is categorized into four classes based on their dehydration temperature (Td) and enthalpy (ΔHd) in analogy with the monotropy/enantiotropy classification for crystal polymorphs. In Class 1 (ΔHd< 0 and Td ≥ 373 K), no awc exists. In Class 2 (ΔHd>0andTd≥373K), awc always exists under conventional crystallization conditions. In Class 3 (ΔHd<0andTd<373K), awc exists when T>Td. In Class 4 (ΔHd>0andTd<373K), awc exists only when T<Td. The hydrate-anhydrate pairs of carbamazepine and theophylline belong to Class 4.

Directed preparation of N-(1-deoxy-d-ribulos-1-yl)-glutathione during short-term high temperature dehydration: Suppressing the side reactions of glutathione

The Amadori rearrangement product (GR-ARP) derived from glutathione/ribose mixture (GSH/Rib) was prepared through spray drying characterized by short-term high temperature dehydration. The water activity of spray-dried samples containing GR-ARP decreased continuously with an intensified degree of dehydration. Lower water activity (from 0.23 to 0.13) and higher GR-ARP yield (from 46.56% to 64.02%) in the spray-dried products were found with the increase of inlet temperature, the slowdown of feed speed, and the alkalization of stock solution. Moreover, during the spray drying and formation of powders, the intensified dissipation of bound water to free water promoted intermolecular condensation that compensated bound water, favoring the directed conversion of GSH/Rib into GR-ARP. Compared to rotary evaporation at 80 °C, spray drying enabled a stronger restraint of amide cleavage and sulfhydryl oxidation in GSH, which reduced the yield of GSH-derived byproducts by 16.39%. Thus, GR-ARP was achieved a peak yield of 64.02% at an initial pH of 7.00 based on more efficient intermolecular condensation and controlled side reactions of GSH when the inlet temperature was set at 170 °C. The spray-dried sample containing richer GR-ARP and other flavor precursors showed a more similar flavor profile to the heated GSH/Rib mixture (complete Maillard reaction products) than other GR-ARP-related thermal processing samples, such as vacuum-dehydrated, GR-ARP, GR-ARP + GSH, and GR-ARP + Rib samples, revealing a great potential of the ARP mixture prepared by spray drying for flavor enhancement.

Utilization of phosphogypsum from industrial dumps as an element of environmentally safe energy- and resource-conserving technologies

The paper discusses the problem of disposal and processing of phosphogypsum dumps as an element of environmentally safe energy- and resource-conserving technologies. The process of impact and possibility of phosphogypsum pre-treatment with weak electric fields to improve its physical and mechanical properties was studied. Two samples of different origin phosphogypsum, which are located in dumps on the territory of the Kamianske City (Ukraine), were used as research material. The research was conducted on samples of the following fractions: 1.0–2.0, 0.4–1.0, 0.1–0.4 mm. Further, balls were formed from the treated phosphogypsum and raw materials to study their compressive strength. The experiment was performed on a pellet strength meter, which operates in the range of 0–2.5 kgf/grain. Phosphogypsum balls, treated with electric current, did not collapse with the maximum values of the device. According to the research results, it was established that preliminary treatment with a low electric current leads to a decrease in the dehydration temperature of phosphogypsum, and the subsequent hydration allows to obtain a material with higher compressive strength properties. This substantiates the potential possibility of involving research results to obtain a cheaper product and will allow to liquidate multi-ton deposits of phosphogypsum.

Dehydration Impact on Antioxidant Potential and Phenolic content of Backhousia citrodora leaves

The most popular method for food preservation is dehydration. In order to enhance the overall quality and prolong the longevity of herbal products, it is imperative to carefully choose optimal dehydration conditions. The dehydration of Backhousia citriodora, also known as lemon myrtle leaves (LML), was conducted via three distinct techniques: conventional dehydration at temperatures of 40, 50, and 60°C (referred to as CD40, CD50, and CD60, respectively); vacuum dehydration at the same temperature as conventional dehydration with a pressure of 50 mbar; and heat pump dehydration at a constant temperature of 45°C. The antioxidant capacities, specifically the radical scavenging activity (DPPH) and ferric reducing antioxidant power (FRAP), along with the total phenolic content (TPC), were evaluated. HPD samples came up second to VD samples in terms of TPC retention, DPPH activity, and FRAP test, whereas CD samples had the lowest biochemical content across all dehydration conditions. The TPC and antioxidant activity in the CD sample exhibited a substantial reduction as the dehydration temperature increased. After dehydration, the CD60 sample had the largest reduction in TPC, DPPH, and FRAP values. Maximising the retention of biochemical content is of utmost importance in post-harvest processing as it serves as an indicator of greater retention. Therefore, the selection of appropriate dehydration techniques and conditions is critical in achieving this objective.

Investigation on the Initial Stage of the Dehydration Process in Mg(OH)2 by Density Functional Theory Calculations.

Mg(OH)2/MgO has been attracting considerable interest as a viable candidate for thermochemical heat storage materials, particularly within the temperature range of 200-400 °C. Nonetheless, the typical dehydration temperature of Mg(OH)2, which occurs within the 300-400 °C range, needs to be reduced to enhance its effectiveness in various applications for thermal energy storage. While several studies have shown that heterospecies doping can lower the dehydration temperature, the fundamental mechanism underlying this effect still remains unclear. Here, we employed density functional theory calculations to elucidate the dehydration mechanism of Mg(OH)2, with a particular focus on the initial stage of the dehydration that determines the temperature beginning the reaction. Our findings indicate that the formation of water molecules on the (001) surface is critical in the early stages of the dehydration. This discovery provides a comprehensive explanation for the role of dopants (Na, Li, or LiCl) in reducing the dehydration temperature by decreasing the formation energy of paired H and OH defects and the migration barrier of H on the surface. The present study will significantly advance the development of novel dopants for Mg(OH)2, facilitating a lower dehydration temperature and, thereby, increasing its suitability for heat storage applications.

Thermogalvanic hydrogel-based e-skin for self-powered on-body dual-modal temperature and strain sensing

Sensing of both temperature and strain is crucial for various diagnostic and therapeutic purposes. Here, we present a novel hydrogel-based electronic skin (e-skin) capable of dual-mode sensing of temperature and strain. The thermocouple ion selected for this study is the iodine/triiodide (I−/I3−) redox couple, which is a common component in everyday disinfectants. By leveraging the thermoelectric conversion in conjunction with the inherent piezoresistive effect of a gel electrolyte, self-powered sensing is achieved by utilizing the temperature difference between the human body and the external environment. The composite hydrogels synthesized from polyvinyl alcohol (PVA) monomers using a simple freeze‒thaw method exhibit remarkable flexibility, extensibility, and adaptability to human tissue. The incorporation of zwitterions further augments the resistance of the hydrogel to dehydration and low temperatures, allowing maintenance of more than 90% of its weight after 48 h in the air. Given its robust thermal current response, the hydrogel was encapsulated and then integrated onto various areas of the human body, including the cheeks, fingers, and elbows. Furthermore, the detection of the head-down state and the monitoring of foot movements demonstrate the promising application of the hydrogel in supervising the neck posture of sedentary office workers and the activity status. The successful demonstration of self-powered on-body temperature and strain sensing opens up new possibilities for wearable intelligent electronics and robotics.

Cobalt-Ion Superhygroscopic Hydrogels Serve as Chip Heat Sinks Achieving a 5°C Temperature Reduction via Evaporative Cooling.

In the rapidly advancing semiconductor sector, thermal management of chips remains a pivotal concern. Inherent heat generation during their operation can lead to a range of issues such as potential thermal runaway, diminished lifespan, and current leakage. To mitigate these challenges, the study introduces a superhygroscopic hydrogel embedded with metal ions. Capitalizing on intrinsic coordination chemistry, the metallic ions in the hydrogel form robust coordination structures with non-metallic nitrogen and oxygen through empty electron orbitals and lone electron pairs. This unique structure serves as an active site for water adsorption, beginning with a primary layer of chemisorbed water molecules and subsequently facilitating multi-layer physisorption via Van der Waals forces. Remarkably, the cobalt-integrated hydrogel demonstrates the capability to harvest over 1 and 5g g-1 atmospheric water at 60% RH and 95% RH, respectively. Furthermore, the hydrogel efficiently releases the entirety of its absorbed water at a modest 40°C, enabling its recyclability. Owing to its significant water absorption capacity and minimal dehydration temperature, the hydrogel can reduce chip temperatures by 5°C during the dehydration process, offering a sustainable solution to thermal management in electronics.

Doping effects on magnesium hydroxide: Enhancing dehydration and hydration performance for thermochemical energy storage applications

Thermochemical energy storage (TCES) holds significant promise owing to its remarkable energy storage density and extended storage capabilities. One of the most extensively studied systems in TCES involves the reversible hydration/dehydration reaction of magnesium hydroxide (Mg(OH)2) to magnesium oxide (MgO). This system suffers from several challenges such as the dehydration temperature of 360 °C, which is considered higher for some applications, low kinetics, and conversion fraction, in addition to the conversion decay after cycles. Nonetheless, it is essential to recognize that each material within thermochemical systems has distinct operational requirements, including temperature and pressure conditions, making them suitable for specific applications. Consequently, the development of materials is a pivotal factor in expanding the effectiveness of sustainable technologies. This research addresses challenges associated with the reversible reaction by partially substituting Mg with transition metal elements like Zn, Ni, Mn, Co, and Cu, leading to the development of new materials Mg1-xMx(OH)2 with x = 0.05. The results indicate successful synthesis of hydroxide systems through coprecipitation. Morphological analysis reveals that material morphology plays a significant role in the performance of thermochemical systems. Additionally, the developed materials demonstrate a reduction in dehydration temperature, reaching 295 °C with cobalt doping. There is also an increase in the conversion reaction, with a 10 % improvement in energy density recorded for the material doped with 5 % Zn. Lastly, the developed materials exhibit good cyclability performance for up to 6 cycles.

Sodium acetate-based thermochemical energy storage with low charging temperature and enhanced power density

The electrification of heat necessitates the development of innovative domestic heat batteries to effectively balance energy demand with renewable power supply. Thermochemical heat storage systems show great promise in supporting the electrification of heating, thanks to their high thermal energy storage density and minimal thermal losses. Among these systems, salt hydrate-based thermochemical systems are particularly appealing. However, they do suffer from slow hydration kinetics in the presence of steam, which limits the achievable power density. Additionally, their relatively high dehydration temperature hinders their application in supporting heating systems. Furthermore, there are still challenges regarding the appropriate thermodynamic, physical, kinetic, chemical, and economic requirements for implementing these systems in heating applications. This study analyzes a proposal for thermochemical energy storage based on the direct hydration of sodium acetate with liquid water. The proposed scheme satisfies numerous requirements for heating applications. By directly adding liquid water to the salt, an unprecedented power density of 5.96 W/g is achieved, nearly two orders of magnitude higher than previously reported for other salt-based systems that utilize steam. Albeit the reactivity drops as a consequence of deliquescence and particle aggregation, it has been shown that this deactivation can be effectively mitigated by incorporating 10 % silica, achieving lower but stable energy and power density values. Furthermore, unlike other salts studied previously, sodium acetate can be fully dehydrated at temperatures within the ideal range for electrified heating systems such as heat pumps (40 °C – 60 °C). The performance of the proposed scheme in terms of dehydration, hydration, and multicyclic behavior is determined through experimental analysis.

Thermochemical heat storage performance of Fe-doped MgO/Mg(OH)2: Experimental and DFT investigation

MgO/Mg(OH)2 thermochemical heat storage system can realize large-scale energy storage by repetitive hydration/dehydration reactions to enhance the stability of solar energy utilization. However, slow interconversion and incomplete reactions caused by agglomeration restrict the cyclic heat storage capability of MgO/Mg(OH)2. In this work, a low-cost efficient Fe-doped MgO was prepared by a simple wet-mixing method and its energy released performance and kinetics in MgO/Mg(OH)2 heat storage progress were examined in a twin fixed-bed reactor and a simultaneous thermal analyzer. Additionally, density functional theory calculations were used to examine the impact of Fe on the mechanisms of MgO/Mg(OH)2 heat storage process. The results shows that when the molar ratio of MgO to Fe is 95:5, the energy released density of Fe-doped MgO is about 400 % higher than that of MgO after 10 heat storage cycles. In preparation process, the existence of Fe leads to the generation of MgFe2O4, which forms layered microstructure with the high specific surface area and pore volume and mitigates agglomeration behavior of MgO. It improves the cyclic stability of MgO and reduces the dehydration temperature of Mg(OH)2, and simultaneously the activation energy of the dehydration stage is reduced by 33.2 %. Fe enhances the interaction of H2O with the MgO surface and promotes the dissociation of H2O on Mg(OH)2 surface. Combined with economic analysis, Fe-doped MgO is a suitable material for MgO/Mg(OH)2 heat storage cycles.