Algorithm for blinds control based on the optimization of blind tilt angle using a genetic algorithm and fuzzy logic

This paper presents the calculation of the power of solar rays that pass through the window of an observed room and their impact on warming up and lighting of the room. The calculations were performed using a mathematical model that takes into account the geographical position of the object, time zone, orientation of windows, day of the year, and current time. This paper also includes the calculation of geometry of the solar radiation and its intensity, artificial light and cooling/heating demands. Based on data from above, the optimization of blind tilt angle was performed to achieve the best possible brightness of the room and energy savings when heating or cooling, depending on ambient temperature. Optimization was performed using a genetic algorithm and fuzzy logic. After an analysis of the results obtained from optimization of the blind tilt angle, an algorithm for blinds control was developed in order to achieve energy savings and comfort in the observed room. Based on the derived conclusions, an UML diagram was made that describes the algorithm for determining optimal blind tilt angle.     

Substitution of nickel in Mg2Ni and its hydride with elements from groups XIII and XIV: An ab initio study

We have performed ab initio calculations with equilibrium supercells of the Mg₂Ni compound and its hydride Mg₂NiH₄ doped with elements X = Al, Ga, In, Si, Ge and Sn. Two concentrations of X in both structures have been set: (1) every 16th, and (2) every fourth Ni atom has been substituted by X. Total energy calculations yielded the Mg₂NiH₄ hydrogen absorption enthalpy ΔH_abs according to the chemical reaction Mg₂Ni + 2H₂ → Mg₂NiH₄. Reduction of the hydrogen absorption enthalpy was reported for both concentrations of X. When doping the Mg₂NiH₄ hydride with X = In in a low concentration (1), the value of hydrogen desorption enthalpy decreases from 68.22 to 55.96 kJ(mol H₂)^?1. Doping with X = In in a high concentration (2) further decreases the hydrogen desorption enthalpy to 5.50 kJ(mol H₂)^?1. Further, the electronic structure of Mg₂(Ni–In)H₄ hydride with a low In concentration indicates weaker Ni–H bonds in comparison with the pristine Mg₂NiH₄. Attraction between H and In atoms induced enhanced bonding between Mg and H atoms compared to the pristine Mg₂NiH₄.     

Review of the environmental policy instruments in the standardization of H2 for the decarbonization of Mexico

The objective of this work is to review the environmental and ecological policy instruments that Mexican legislation for existence of an Official Mexican Hydrogen Standard according to the premises motivates decarbonization. There is a worldwide interest in hydrogen (H₂) and its incorporation into legal systems. In Mexico there are large legal gaps that question the legality of H₂, because it is not recognized in a federal law and is only considered in technical standards of voluntary application. Also, Mexico has forest, agricultural, and livestock waste that, if properly used, can cover the energy demand of communities. The main findings of this study refer to the fact that, according to international standards for the management of H₂ and taking into account the regulatory limitations in Mexico, it is possible to promote, an Official Mexican Standard exclusively aimed at establishing the minimum requirements for the design, construction, operation and maintenance of H₂ storage, considering the areas of the opportunity offered by foreign experiences, according to the Mexican context. It is concluded that the parameters of legality exist in the instruments of environmental policy, to support the existence of an Official Mexican Standard of H₂.     

Detailed microkinetic modelling of syngas to hydrocarbons via Fischer Tropsch synthesis over cobalt catalyst

Fuels production from syngas via Fischer Tropsch synthesis (FTs) is an alternative technology for clean energy production. The microkinetic model is a promising approach for gaining insight into FTs activity. In this study, a systematic microkinetic model was proposed to develop a process for cobalt-catalyzed FTs. All possible elementary reactions based on the carbide mechanism and characteristics of catalyst sites were considered in the kinetic model. The effects of the reaction rate constant, reaction pathways, and H₂ to CO ratio were represented by a kinetic parameter, reaction path, and operating parameter, respectively. The model could accurately predict product distribution trends, with an R² value and mean absolute relative residuals percentage of 0.91–0.93 and 5–43%, respectively, in comparison with experimental data. Hydrogen utilization was predicted and analyzed. High model accuracy was achieved, with a 10^?10–10^?3% error in the material balance.     

Mechano-chemical synthesis of manganese borohydride (Mn(BH4)2) and inverse cubic spinel (Li2MnCl4) in the (nLiBH4 + MnCl2) (n = 1, 2, 3, 5, 9 and 23) mixtures and their dehydrogenation behavior

Manganese borohydride (Mn(BH₄)₂) was successfully synthesized by a mechano-chemical activation synthesis (MCAS) from lithium borohydride (LiBH₄) and manganese chloride (MnCl₂) by applying high energy ball milling for 30 min. For the first time a wide range of molar ratios n = 1, 2, 3, 5, 9 and 23 in the (nLiBH₄ + MnCl₂) mixture was investigated. During ball milling for 30 min the mixtures release only a very small quantity of H₂ that increases with the molar ratio n but does not exceed ∼0.2 wt.% for n = 23. However, longer milling duration leads to more H₂ released. For the equimolar ratio n = 1 the principal phases synthesized are Li₂MnCl₄, an inverse cubic spinel phase, and the Mn(BH₄)₂ borohydride. For n = 2 a LiCl salt is formed which coexists with Mn(BH₄)₂. With the n increasing from 3 to 23 LiBH₄ is not completely reacted and its increasing amount is retained in the microstructure coexisting with LiCl and Mn(BH₄)₂. Gas mass spectrometry during Temperature Programmed Desorption (TPD) up to 450 °C shows the release of hydrogen as a principal gas with a maximum intensity around 130–150 °C accompanied by a miniscule quantity of borane B₂H₆. The intensity of the B₂H₆ peak is 200–600 times smaller than the intensity of the corresponding H₂ peak. In situ heating experiments using a continuous monitoring during heating show no evidence of melting of Mn(BH₄)₂ up to about 270–280 °C. At 100 °C under 1 bar H₂ pressure the ball milled n = 2 and 3 mixtures are capable of desorbing quite rapidly ∼4 wt.% H₂ which is a very large amount of H₂ considering that the mixture also contains 2 mol of LiCl salt. The H₂ quantities experimentally desorbed at 100 and 200 °C do not exceed the maximum theoretical quantities of H₂ expected to be desorbed from Mn(BH₄)₂ for various molar ratios n. It clearly confirms that the contribution from B₂H₆ evolved is negligibly small (if any) when desorption occurs isothermally in the practical temperature range 100–200 °C. It is found that the ball milled mixture with the molar ratio n = 3 exhibits the highest rate constant k and the lowest apparent activation energy for dehydrogenation, E_A ∼ 102 kJ/mol. Decreasing or increasing the molar ratio n below or above 3 increases the apparent activation energy. Ball milled mixtures with the molar ratio n = 2 and 3 discharge slowly H₂ during storage at room temperature and 40 °C. The addition of 5 wt.% nano-Ni with a specific surface area of 60.5 m²/g substantially enhances the rate of discharge at 40 °C.     

Exergy analysis of the diesel pre-reforming solid oxide fuel cell system with anode off-gas recycling in the SchIBZ project. Part I: Modeling and validation

Solid oxide fuel cell (SOFC) systems with anode off-gas recirculation (AGR) and diesel pre-reforming are advantageous because they can operate with the current fuel infrastructure. In the SchIBZ-project, the prototype of such a SOFC system for maritime applications has already been commissioned. In this first paper, we model the system devices to conduct an exergy analysis of this real SOFC plant and validate them with experimental values from experiments in laboratory scale. The results of our simulation agree well with the experimental values. The calculations with the validated results may be closer to the real thermodynamic behavior of such system components than previous literature.     

Hydrogen gas sensing properties of WO3 sputter-deposited thin films enhanced by on-top deposited CuO nanoclusters

Magnetron-based gas aggregation cluster source (GAS) was used to prepare high-purity CuO (cupric oxide) nanoclusters on top of sputter-deposited thin film of tungsten trioxide (WO₃). The material was assembled as a conductometric hydrogen gas sensor and its response was tested and evaluated. It is demonstrated that addition of CuO clusters noticeably enhances the sensitivity of the pure WO₃ thin film. With an increasing amount of CuO clusters the sensitivity of CuO/WO₃ system rises further. When CuO clusters form a sufficiently thick and compact layer, the resistance response is reversed. Based on the sensorial behavior, conventional and near-ambient pressure X-Ray photoemission spectroscopies, and resistivity measurements, we propose that the sensing mechanism is based on the formation of nano-sized p-n junctions in between p-type CuO and n-type WO₃. The advantages of the GAS technique for preparing sensorial and/or catalytically active materials are emphasized.     

Surface charge and function of cellulose battery separators

The results of zeta-potential determination using the electro-osmotic method in dilute (10^–3 mol dm^–3) solutions of NH₄Cl and ZnCl₂ and diffusion parameters measured in 20% NH₄Cl and 30% ZnCl₂ solutions are presented. In both cases cellulosic membrane separators from different manufacturers, already in practical usage in Leclanché cells, were examined. From the measured data, diffusion potentials were calculated and compared with experimental values. Transport numbers calculated from diffusion potentials are compared to values in free solution (i.e. without a membrane). The relevance of these parameters to the role of cellulosic separators in Leclanché-type cells is briefly discussed.