Search Results (49)

Hydrogen is considered one of the most promising energy carriers for sustainable and carbon-neutral energy systems. However, the large-scale deployment of hydrogen technologies is limited by the lack of efficient, safe, and cost-effective hydrogen storage methods. This review examines current hydrogen storage technologies and the physical and chemical mechanisms underlying hydrogen adsorption. Traditional storage approaches, including compressed gas and liquid hydrogen, are briefly analyzed with respect to their advantages, limitations, safety concerns, and energy requirements. Special focus is given to solid-state hydrogen storage systems based on metal hydrides, which offer high storage capacities and enhanced operational safety. Recent advances in intermetallic hydrides, magnesium-based materials and complex hydrides are discussed, along with challenges related to thermodynamic stability, sorption kinetics, thermal management, and cycling durability. This review also highlights recent developments in nanoporous carbon materials and the role of the hydrogen spillover mechanism in improving adsorption performance. Experimental studies reporting hydrogen adsorption capacities above 7 wt.% and up to 11.2 wt.% are analyzed. Based on the reviewed literature, key research directions are identified for optimizing the adsorption properties of advanced materials and accelerating the development of efficient and sustainable hydrogen storage technologies for future energy applications. Full article

Metal hydrides can safely store hydrogen in the solid state at high volumetric density under moderate temperature and pressure. Their hydrogen sorption characteristics are represented by pressure–composition–temperature (PCT) curves. AB₅–type metal hydrides, which have low plateau pressures, store and release hydrogen at low pressures. AB₂–type metal hydrides, which have high plateau pressures, store and release hydrogen at relatively high pressures. Compared with AB₅–type metal hydrides, AB₂–type metal hydrides generally have lower raw material costs and higher hydrogen storage capacity. This makes them more suitable for storing large quantities of hydrogen. Green and blue hydrogen are produced using commercial alkaline water electrolyzers and natural gas reformers, respectively. After downstream purification, this hydrogen is typically supplied at pressures below 1 MPa. However, the high plateau pressures of AB₂–type metal hydrides make it difficult to store this low-pressure hydrogen directly. AB₅–type metal hydrides can store it but release it only at low pressures. A single hydride type therefore operates within a narrow pressure range for both storage and delivery. In this study, a multipurpose hydrogen storage system (MHSS) using AB₅– and AB₂–type metal hydrides was proposed to broaden the applications of metal hydride-based systems. The feasibility of the MHSS was experimentally evaluated through lab-scale tests. The AB₅ and AB₂ modules were first tested as standalone units. The integrated MHSS was then tested assuming that waste heat was continuously available. The MHSS can store a large quantity of low-pressure hydrogen and deliver it across a wide pressure range. This range covers diverse end uses, from fuel cells at 0.5 MPa to hydrogen pipelines at 4.0 MPa. Full article

Hydrogen is increasingly seen as a viable energy carrier in the transition to low-carbon energy systems, mainly because of its high gravimetric energy density and the absence of carbon emissions at the point of use. In this context, producing hydrogen from biomass represents a practical and sustainable option, as it allows the use of renewable and waste resources while supporting circular economy principles. This work examines the main pathways for hydrogen production from biomass, considering both thermochemical and biochemical routes, with a focus on their energy performance and practical limitations. The analysis shows that thermochemical processes, particularly gasification, remain the most developed and scalable solutions for converting solid biomass into hydrogen-rich gas, although their performance depends strongly on feedstock properties, reactor design, and operating conditions. By comparison, biochemical processes such as dark fermentation and photofermentation are more suitable for wet biomass but are limited by lower hydrogen yields and issues related to process stability. From a thermal engineering standpoint, system performance is influenced by heat transfer constraints, the energy demand of endothermic reactions, and the efficiency of gas cleaning, while parameters such as temperature, steam-to-biomass ratio, and equivalence ratio play a key role in optimization. Advanced approaches, including catalytic and sorption-enhanced gasification, show potential for improving performance. Overall, efficient hydrogen production requires a system-level approach, as no single technology can be considered universally optimal. Full article

While advanced imaging techniques and ordered porous materials like MOFs have gained prominence, gas sorption remains the indispensable tool for characterizing the multiscale heterogeneity of industrially important disordered solids, such as catalysts and shales. This review examines recent developments in gas sorption methodologies specifically tailored for rigid, disordered porous media. We discuss experimental advances, including the choice of adsorbate and the utility of the overcondensation method for probing macroporosity and ensuring saturation. Furthermore, we critically evaluate theoretical approaches for determining pore size distributions (PSDs), contrasting classical methods with Density Functional Theory (DFT) and Grand Canonical Monte Carlo (GCMC) simulations. Special emphasis is placed on the impact of pore-to-pore cooperative effects, such as advanced condensation, cavitation, and pore-blocking, on the interpretation of sorption isotherms. We highlight how complementary techniques, including integrated mercury porosimetry, NMR, and computerized X-ray tomography (CXT), are essential for deconvolving these complex network effects and validating void space descriptors. We conclude that, while “brute force” molecular simulations on image-based reconstructions are progressing, “minimalist” pore network models, which incorporate cooperative mechanisms, currently offer the most empirically adequate approach. Ultimately, gas sorption remains unique in its ability to statistically characterize void spaces from Angstroms to millimeters in a single experiment. Full article

This study presents the experimental and thermodynamic evaluation of a solar thermochemical refrigeration system (STRS) powered by evacuated tube solar collectors with heat pipes as thermal energy sources, using industrial-grade BaCl₂–NH₃. The system was designed to produce refrigeration and ice using industrial-grade BaCl₂–NH₃ without additional additives or electrical input. Experimental tests were conducted under real-world conditions, with generation temperatures between 55 and 66 °C and solar irradiance of 750 to 900 W/m². The system achieved efficient ammonia desorption, yielding up to 4.2 L of refrigerant and demonstrating repeatable operation over several thermochemical cycles. During the nighttime absorption–evaporation process, the STRS reached evaporation temperatures of −7 to −3 °C and absorption temperatures between 24 and 31 °C, suitable for ice production. The internal coefficient of performance ranged from 0.244 to 0.307, with an overall efficiency of 0.146 to 0.206. The experimental data obtained were used to derive pressure–temperature equilibrium equations for the BaCl₂–NH₃ working pair, yielding correlation coefficients greater than 0.98, which confirms thermodynamic consistency. The results demonstrate that additive-free, industrial-grade BaCl₂ can achieve high efficiency at low temperatures, making this system a cost-effective and sustainable alternative for refrigeration and cold storage in rural areas. This research contributes new experimental knowledge on low-temperature thermochemical refrigeration and supports future development toward quasi-continuous optimization cycles based on experimental data. Full article

Unsymmetrical dimethylhydrazine (UDMH), a highly toxic rocket propellant, remains a significant environmental concern in Kazakhstan due to repeated rocket stage falls near the Baikonur Cosmodrome. This study integrates chemical analysis with stochastic contamination transport modeling to evaluate the persistence and migration of UDMH transformation products (TPs) in soils collected 15 years after the rocket crash. Vacuum-assisted headspace solid-phase microextraction coupled with gas chromatography–mass spectrometry (Vac-HS-SPME-GC-MS) was used to determine five major TPs. Among these, pyrazine (PAN) and 1-methyl-1H-pyrazole (MPA) were consistently detected at concentrations ranging from 0.04–2.35 ng g⁻¹ and 0.06–3.48 ng g⁻¹, respectively. Stochastic simulations performed with HYDRUS-1D indicated that the long-term persistence of these compounds is mainly controlled by physical nonequilibrium transport processes, including diffusion-limited exchange, weak sorption, and slow inter-domain mass transfer, rather than by degradation. Sensitivity analysis demonstrated that low dispersivity and diffusion coefficients enhance solute retention within immobile domains, maintaining residual levels over extended periods. The results demonstrate the efficacy of combined long-term monitoring and predictive modeling frameworks for assessing contamination dynamics in rocket impact zones. Full article

TiVCr-based alloys are well-explored body-centered cubic (BCC) materials for hydrogen storage applications that can potentially store higher amounts of hydrogen at moderate temperatures. The challenge remains in optimizing the alloy-hydrogen stability, and several transition elements have been found to support the reduction in the hydride stability. In this study, Ni and Nb transition elements were incorporated into the TiVCr alloy system to thoroughly understand their influence on the (de)hydrogenation kinetics and thermodynamic properties. Three different compositions, (TiVCr)₉₅Ni₅, (TiVCr)₉₀ Ni₁₀, and (TiVCr)₉₅Ni₅Nb₅, were prepared via arc melting. The as-prepared samples showed the formation of a dual-phase BCC solid solution and secondary phase precipitates. The samples were characterized using hydrogen sorption studies. Among the studied compositions, (TiVCr)₉₀Ni₁₀ exhibited the highest hydrogen absorption capacity of 3 wt%, whereas both (TiVCr)₉₅Ni₅ and (TiVCr)₉₀Ni₅Nb₅ absorbed up to 2.5 wt% hydrogen. The kinetics of (de)hydrogenation were modeled using the JMAK and 3D Jander diffusion models. The kinetics results showed that the presence of Ni improved hydrogen adsorption at the interface level, whereas Nb substitution enhanced diffusion and hydrogen release at room temperature. Thus, the addition of Ni and Nb to Ti-V-Cr-based high-entropy alloys significantly improved the hydrogen absorption and desorption properties at room temperature for gas-phase hydrogen storage. Full article

This review analyzes the current practices in the data-driven characterization, design and optimization of disordered nanoporous materials with pore sizes ranging from angstroms (active carbon and polymer membranes for gas separation) to tens of nm (aerogels). While the machine learning (ML)-based prediction and screening of crystalline, ordered porous materials are conducted frequently, materials with disordered porosity receive much less attention, although ML is expected to excel in the field, which is rich with ill-posed problems, non-linear correlations and a large volume of experimental results. For micro- and mesoporous solids (active carbons, mesoporous silica, aerogels, etc.), the obstacles are mostly related to the navigation of the available data with transferrable and easily interpreted features. The majority of published efforts are based on the experimental data obtained in the same work, and the datasets are often very small. Even with limited data, machine learning helps discover non-evident correlations and serves in material design and production optimization. The development of comprehensive databases for micro- and mesoporous materials with low-level structural and sorption characteristics, as well as automated synthesis/characterization protocols, is seen as the direction of efforts for the immediate future. This paper is written in a language readable by a chemist unfamiliar with the data science specifics. Full article

In the chemical industry and in the manufacturing sector, the adsorption properties of porous materials have been proven to be of great interest for the removal of impurities from liquid and gas media. While it is acknowledged that significant progress and literature production have been developed in this field, there have been adsorption studies that failed to further advance our knowledge in generating a better understanding of the prevailing sorption types and dominant adsorption processes. Therefore, this review study has focused on porous materials, their sorption types and their adsorption properties, further investigating the adsorption properties of porous materials at either solid–gas and solid–liquid interfaces, underscoring both the properties of the materials, the characterization and the correlation between the porosity and the adsorption capacity, as well as the emergent interactions between the adsorbent and adsorbate molecules, including the adsorption mechanisms, the types of sorption and the kinetic and thermodynamic information conveyed. Full article

The fluidization of two different solids was investigated by varying the temperature and pressure conditions and the fluidizing gas. The solids are a novel catalyst and a water sorbent that could be used to perform sorption-enhanced methanol synthesis; the operating conditions were selected accordingly to this process. The aim of this investigation was to find an expression for predicting the minimum fluidization conditions of a methanol synthesis catalyst and an adsorbent in the presence of their process stream and operating conditions. The findings of this study highlighted how u_mf (STP) decreases with a rise in temperature and increases with a rise in pressure, according to other works in the literature with different solids. Furthermore, the type of gas was found to influence the minimum fluidization velocity significantly. The experimental results agreed well with a theoretical expression of the minimum fluidization velocity adjusted for temperature, pressure, and viscosity. The choice of the expression for viscosity calculation in the case of gas mixtures was found to be of key importance. These results will be useful for researchers aiming to calculate the minimum fluidization velocity of a catalyst or other solids under reaction conditions using results obtained at ambient conditions with air or inert gas. Full article

α-CD:N₂O “host-guest” type complexes were formed by a simple solid–gas reaction (N₂O sorption into α-CD) under different gas pressures and temperatures. The new N₂O inclusion method applied in the present study was compared with the already known technique based on the crystallization of clathrates from a water solution of α-CD saturated with N₂O. A maximum storage capacity of 4.5 wt.% N₂O was achieved when charging the cyclodextrin from a gas phase. The amount of included gas decreases to 1.3 wt.% when the complex is stored in air at 1 atm and room temperature, analogous to that achieved by the crystallization of α-CD:N₂O. Furthermore, it was shown that the external coordination of N₂O to either the upper or lower rim of α-CD without hydration water displacement is the preferred mode of binding, due to hydrogen bonds with neighboring -OH groups from the host macrocycle and three of the hydration water molecules nearby. The capacity of α-CD to store N₂O and the thermal stability of the α-CD:N₂O complex demonstrated promising applications of these types of complexes in food and beverages. Full article

CO₂ trapping and methanation allow to reduce greenhouse gas emissions and recycle CO₂ into a sustainable fuel, provided renewable H₂ is employed. Microwave (MW)-based reactors provide an efficient means to use electrical energy for upgrading chemicals, since MW can selectively heat up the load placed in the reactor and not the reactor itself. In this study, CO₂ capture and methanation were investigated using solid adsorbents (ZrO₂ and Fe₃O₄), microwave absorbers (SiC and Fe₃O₄) and Ru/SiO₂ as CO₂ the methanation catalyst. The sorption and catalyst beds were located in a domestic MW oven that was used to trigger CO₂ desorption and methanation in the presence of H₂. The working Fe-based structure turned out to be a mixture of FeO and Fe, which allowed for MW absorption and local heating; it also acted as a CO₂ sorbent and reverse water–gas shift catalyst. Various reactor configurations were used, leading to different performances and selectivity to CO and CH₄. To the best of our knowledge, this is the first report of its kind showing the potential of using inexpensive microwave technology to readily convert trapped CO₂ into valuable products. Full article

In this work, ASPENplus was used to simulate biogas upgrading by sorption-enhanced methanation in a dual interconnected bubbling fluidized bed configuration using inexpensive, abundant, and eco-friendly CaO to remove H₂O from the reaction environment. The chemical looping scheme consisted of two reactors: a methanator/hydrator, where the catalytic reactions occurred on a catalyst with 20% Ni supported on alumina as well as the steam removal by CaO, and a regenerator, where the Ca(OH)₂ was dehydrated back to CaO. The simulations were carried out to identify possible reactant compositions (H₂ and biogas), CaO amount, and the methanation temperature able to produce an outlet gas matching the specifications for direct grid injection. When considering a stoichiometric gas feed ratio at the methanator inlet, the unwanted CaO carbonation worsened the process performance, subtracting CO₂ from the desired methanation reaction. However, optimal conditions were found with hydrogen-lean gas feedings, balancing the limited H₂ amount with the capture of CO₂ due to the sorbent carbonation. Thermodynamic considerations pointed out the possibility of solid carbon formation induced by sorption-enhanced methanation conditions, especially for H₂ sub-stoichiometric feedings. Full article

Milk is an important and necessary food product for reducing morbidity in the human body. There are numerous misconceptions around milk and dairy products in this regard. At the same time, one of the most time-consuming indicators of raw milk comprises its microbiological parameters. The purpose of this research is to study the gas phase of raw milk samples, using piezoelectric sensors with polycomposite coatings, to predict its physicochemical or microbiological properties. The sorption of volatile compounds onto the coatings based on chitosan–micellar-casein concentrate with polymeric sorbents was studied. This array was employed to analyze the gas phase over raw milk samples. It evaluated the physicochemical indicators of milk (the contents of fat, protein, and solid substances; the acidity) and the microbiological indicators (the total microbial count; the presence of mold, yeasts, or pathogenic microorganisms). The influence of several factors on the composition of volatile compounds in milk was evaluated using the output data of the sensors. These are the injector or frontal mode of inputting the gas phase into the detection cell, the processing of milk samples via ultrasound and microwave radiation, and the introduction of glucose and hydrogen peroxide additives into samples. Statistically significant correlations have been established between the sensor output data and the physicochemical or microbiological indicators of raw milk samples. The regression model was constructed using partial least squares regression to predict the total microbial count of milk based on the output data of piezoelectric sensors with composite coatings, with an appropriate error. Full article

Poly(methyl methacrylate) (PMMA) is characterized by high CO₂ capture yield under mild pressures and temperatures. A morphological modification of powdery amorphous PMMA (pPMMA) is carried out by electrospinning to increase the surface/volume ratio of the resulting electrospun PMMAs (ePMMAs). This modification improves the kinetics and the capture yields. The rate constants observed for ePMMAs are two to three times higher than those for pPMMA, reaching 90% saturation values within 5–7 s. The amount of sorbed CO₂ is up to eleven times higher for ePMMAs at 1 °C, and the highest difference in captured CO₂ amount is observed at the lowest tested pressure of 1 MPa. The operating life of the ePMMAs shows a 5% yield loss after ten consecutive runs, indicating good durability. Spent electrospun PMMAs after several cycles of CO₂ sorption-desorption can be regenerated by melting and again electrospinning the molten mass, resulting in a CO₂ capture performance that is undistinguishable from that observed with fresh ePMMA. Scanning electron and atomic force microscopies show a reduction in surface roughness after gas exposure, possibly due to the plasticization effect of CO₂. This study shows the potential of electrospun PMMAs as solid sorbents for carbon capture from natural gas or pre-combustion and oxyfuel combustion processes. Full article