For a material to be used as energy, understanding its combustion behavior is crucial. Biomass is one such material that is increasingly gaining traction. Biomass may be utilized by direct combustion or transformation into fluid or solid biomass-based fuels. In this work, slow pyrolysis of groundnut shells, bagasse, rice husks and coffee husks was done to produce briquettes with cassava starch binder. Thermogravimetric analysis (TGA) was carried out using an Eltra Thermostep thermogravimetric analyzer. The samples were heated from ambient to 920 deg. Celsius. This analysis provided combustion explanations in terms of the weight loss, burning rates, peak temperatures, char residues and mean reactivity. TGA results showed that binder inclusion reduced the amount of fixed carbon present in the developed briquettes, thus slightly reducing their calorific values. Rice husks briquettes yielded the least weight loss (20.9% and 24.7% for 30g and 50g binder incorporations respectively) compared to others, owing to former’s higher ash contents. Increase in binder contents reduced the amount of char residues, caused by reducing ash contents in the developed briquettes. Peak temperatures and char residues generally increased with increasing binder content. This signifies increasing thermal stabilities of the developed briquettes. Highest char residues were obtained by briquettes developed with rice husks at 30g binder while briquettes developed with bagasse briquettes developed at 50g binder had the least char residues. The highest mean reactivities were obtained in briquettes developed from bagasse and coffee husks while briquettes developed from rice husks had lowest mean reactivities. Briquettes developed in this study showed sufficient combustion properties suitable to provide energy for domestic and industrial applications.

This study reports on the effect of introducing TiO2 compact layer on the photovoltaic characteristics of TiO2/Nb2O5 composite dye sensitized solar cell. The compact layer was deposited by spray pyrolysis technique. It was observed that introduction of 60 nm thick compact layer improved the short circuit current density Jsc ,Open circuit voltage Voc, and efficiency of the cell from 4.9 mA/cm2 to 8.2 mA/cm2, 6.8×10-1 V to 7.2×10-1 V and 1.9 % to 3.4 % respectively compared to traditional cell prepared without compact layer. Electrochemical impedance spectroscopy confirmed an increase in recombination resistance from 5.5×101 Ω.cm2 for bare DSSC to 9.0×101 Ω.cm2 for DSSC with compact layer thereby improving electron lifetime of the cells from 2.5×10-4 s to 386.9×10-4 s.

Magnesium hydride (MgH2) is a prospective material for the storage of hydrogen in solid materials. It can also be envisaged for thermal energy storage applications since it has the potential to reversibly absorb hydrogen in large quantities, theoretically up to 7.6% by weight. Also, MgH2 is inexpensive, abundant, and environmentally friendly, but it operates at relatively high temperatures, and the kinetics of the hydrogenation process is slow. Mechanical milling and the addition of catalyst can alter the activation energy and the kinetic properties of the MgH2 phase. It is known that the addition of titanium hydride (TiH2) lowers the enthalpy and enhances the absorption of hydrogen from MgH2, titanium oxide (TiO2) enhances the desorption of hydrogen and niobium oxide (Nb2O5) enhances the absorption of hydrogen. In this work, the influences of the catalysts, as mentioned above on the properties of MgH2, were studied. The samples were analyzed in terms of crystal and microstructure as well as hydrogen storage properties using a pressure-composition isotherm (PCT)measurement. It has been found that the simultaneous addition of the three catalysts enhances the properties of MgH2, lowers the activation energy and operating temperature, increases the rate of intake and release of hydrogen, and provides the largest gravimetric hydrogen storage capacity.

The Ti-Zr-Ni quasicrystal alloys have prospected to be one of the promising materials for hydrogen storage. This is because this type of quasicrystal contains 140 interstitial sites (T-sites) constituted in the Bergman Cluster that could accommodate hydrogen. The number of available sites is far greater than the number found in regular crystals, therefore the improvement of hydrogen storage capacity could be expected. For this study, we focus on the effect of substitution of Cr, in place of Ni in Ti-Zr-Ni amorphous and quasicrystal alloys. The studied samples are synthesized by the combination of mechanical alloying and sintering process. The subsequent measurements of electrochemical hydrogenation and dehydrogenation are carried out by a three-electrode cell at room temperature. The studied samples are structurally characterized by X-ray diffraction and their morphology is analyzed by scanning electron microscope and transmission electron microscope. The influence of the 4th substituted element on the possibility of a new-formed Cr quasicrystalline phase and the potential improvement of hydrogenation and dehydrogenation kinetics for both amorphous and quasicrystalline phase is evaluated. Our measurements showed the maximum discharge capacity achieved by Ti45Zr38Ni7Cr10 amorphous and Ti45Zr38Ni12Cr5 i-phase electrodes at a current density of 15 mA·g-1 to be 9.8 mAh·g-1and 55.2 mAh·g-1 respectively. The maximum estimated H/M value for the Ti45Zr38Ni12Cr5 i-phase electrode reached 1.36. These results are encouraging and show the merit of the usage of quasicrystals as hydrogen storage materials.