Physical Analysis and Mathematical Modeling of the Hydrogen Storage Process in the MmNi4.2Mn0.8 Compound.

The results of an experimental and mathematical study into the MmNi4.2Mn0.8 compound's hydrogen storage properties are presented in the present research. Plotting and discussion of the experimental isotherms (P-C-T) for different starting temperatures (288 K, 298 K, 308 K, and 318 K) were carried out first. Then, the enthalpy and entropy of formation (ΔH0, ΔS0) were deduced from the plot of van't Hoff. Following that, the P-C-T were contrasted with a mathematical model developed via statistical physics modeling. The steric and energetic parameters, such as the number of the receiving sites (n1, n2), their densities (Nm1, Nm2), and the energy parameters (P1, P2) of the system, were calculated thanks to the excellent agreement between the numerical and experimental results. Therefore, plotting and discussing these parameters in relation to temperature preceded their application in determining the amount of hydrogen in each type of site per unit of metal ([H/M]1, [H/M]2) as well as for the entire system [H/M] versus temperature and pressure besides the absorption energies associated with each kind of site (ΔE1, ΔE2) and the thermodynamic functions (free energy, Gibbs energy, and entropy) that control the absorption reaction.

Experimental and numerical study of temperature evolution and hydrogen desorption process on an amorphous alloy Mg50Ni50.

In the present study, we explored the temperature evolution and hydrogen desorption properties of the Mg50Ni50 alloy through both numerical simulation and experimental analyses. Desorption kinetics characterization was carried out using the volumetric method, specifically employing a Sievert's-type apparatus to investigate solid-gas reactions. The experiments covered a temperature range from 313 K to 353 K, with an initial hydrogen pressure of 12 bar. Simultaneously, a mathematical approach was employed to numerically investigate the temperature evolution within the hydride bed. Using COMSOL Multiphysics as a simulator, a numerical simulation was conducted based on experimental data. The study examined the impact of cooling temperature on hydride temperature evolution. Results revealed that hydrogen desorption kinetics of the amorphous Mg50Ni50 alloy are more significant compared to those of Mg2Ni compounds. Moreover, the effect of the warming temperature on the equilibrium pressure can also be observed in the hydrogen desorption isotherm curves. The experimental study of the Mg50Ni50 alloy provided activation energy data, along with determination of hydride formation enthalpy and entropy. On the other hand, we showed that the hydride temperature is maximum at the hydride-hydrogen interface within the hydride center.

A study of the magnetic properties of LaNi5 and their effect on hydrogen desorption under theaction of a magnetostatic field.

A study of the magnetic properties of LaNi5 intermetallic compoundand and their effect on desorption reaction was carried out as a function of temperature. A Vibrating Sample Magnetometer (VSM) was used for the magnetic measurements and a Metal Hydrogen Reactor (MHR) supplied by a constant current through a coil was used for the hydrogen desorption reaction under the action of a magnetostatic field. Then, the hysteresis cycle, the first magnetization curve, the thermo-magnetization curves and the desorbed hydrogen mass were determined. The results showed that the application of a magnetic field corresponding to the magnetization at saturation Ms at a given temperature improved the hydrogen desorption reaction by the LaNi5.

Experimental and Theoretical Studies of Hydrogen Storage in LaNi4.4Al0.3Fe0.3 Hydride Bed.

In this article, the experimental measurements of the absorption/desorption P-C-T isotherms of hydrogen in the LaNi4.4Fe0.3Al0.3 alloy at different temperatures and constant hydrogen pressure have been studied using a numerical model. The mathematics equations of this model contain parameters, such as the two terms, nα and nß, representing the numbers of hydrogen atoms per site; Nmα and Nmß are the receptor sites' densities, and the energetic parameters are Pα and Pß. All these parameters are derived by numerically adjusting the experimental data. The profiles of these parameters during the absorption/desorption process are studied as a function of temperature. Thereafter, we examined the evolution of the internal energy versus temperature, which typically ranges between 138 and 181 kJmol-1 for the absorption process and between 140 and 179 kJmol-1 for the desorption process. The evolution of thermodynamic functions with pressure, for example, entropy, Gibbs free energy (G), and internal energy, are determined from the experimental data of the hydrogen absorption and desorption isotherms of the LaNi4.4Al0.3Fe0.3 alloy.

Experimental study of the microstructures and hydrogen storage properties of the LaNi4Mn0·5Co0.5 alloys.

In the present study, the absorption and desorption kinetics of hydrogen and the isotherm (P-C-T)) of the LaNi4Mn0·5Co0.5 alloy were measured at values of 283 K, 303 K, and 313 K. The morphological states of this sample were examined using characterization techniques, including X-ray diffraction and scanning electron microscopy. The thermodynamic functions for the absorption-desorption of hydrogen by hydrides, such as enthalpy (H) and entropy (S), were calculated from the experimental data or by using a model that exists in the literature and is premised on the adjustment of isotherm curves at various temperatures. This model is based on an integrated form of the Van't Hoff equation and a simultaneous examination of the isotherms. According to the experimental results, the amount of hydrogen absorbed or desorbed by the sample is significantly affected by the partial substitution of the nickel atom by the elements Mn and Co. However, this substitution increased the absorption or de-sorption plateau pressure.

Experimental and theoretical study of CO2 adsorption by activated clay using statistical physics modeling.

The objective of this paper was to study CO2 adsorption on activated clay in the framework of geological storage. The activation of clay was characterized via scanning electron microscopy, N2 adsorption-desorption isotherms, and X-ray diffraction. The adsorption isotherms were generated at different temperatures, namely, 298 K, 323 K, and 353 K. Based on the experimental result, a new model was simulated and interpreted using a multi-layer model with two interaction energies. The physicochemical parameters that described the CO2 adsorption process were determined by physical statistical formalism. The characteristic parameters of the CO2 adsorption isotherm such as the number of carbon dioxide molecules per site (n), the receptor site densities (NM), and the energetic parameters were investigated. In addition, the thermodynamic functions that governed the adsorption process such as the internal energy, entropy, and Gibbs free energy were determined by a statistical physics model. Thus, the results showed that CO2 adsorption on activated clay was spontaneous and exothermic in nature.