Abstract

The chemical hydrogen storage properties of ferrosilicon were investigated. A hydrogen yield of ~4.75 wt.% (with respect to the mass of ferrosilicon) was estimated by the reaction of varying quantities of ferrosilicon with 5 mL of 40 wt.% sodium hydroxide solution. The reaction of ferrosilicon with aqueous sodium hydroxide solution to form hydrogen was found to have an activation energy of 90.5 kJ mol−1 by means of an Arrhenius plot. It was observed that the induction period of the hydrogen generation reaction varies exponentially with temperature. Although this combination of high activation energy and a lengthy induction period at low temperatures reduces the attractiveness of ferrosilicon for portable hydrogen storage applications unless methods can be developed to accelerate the onset and rate of hydrogen generation, its low cost and widespread availability make it attractive for further studies focused on higher temperature stationary applications.

Abstract

It is clear that in order to satisfy global energy demands whilst maintaining sustainable levels of atmospheric greenhouse gases, alternative energy sources are required. Due to its high chemical energy density and the benign by-product of its combustion reactions, hydrogen is one of the most promising of these. However, methods of hydrogen storage such as gas compression or liquefaction are not suitable for portable or automotive applications due to their low hydrogen storage densities. Accordingly, much research activity has been focused on finding higher density hydrogen storage methods. One such method is to generate hydrogen via the hydrolysis of aqueous sodium borohydride (NaBH4) solutions, and this has been heavily studied since the turn of the century due to its high theoretical hydrogen storage capacity (10.8 wt%) and relatively safe operation in comparison to other chemical hydrides. This makes it very attractive for use as a hydrogen generator, in particular for portable applications. Major factors affecting the hydrolysis reaction of aqueous NaBH4 include the performance of the catalyst, reaction temperature, NaBH4 concentration, stabilizer concentration, and the volume of the reaction solution. Catalysts based on noble metals, in particular ruthenium (Ru) and platinum (Pt), have been shown to be particularly efficient at rapid generation of hydrogen from aqueous NaBH4 solutions. However, given the scarcity and expense of such metals, a transition metal-based catalyst would be a desirable alternative, and thus much work has been conducted using cobalt (Co) and nickel (Ni)-based materials to attempt to source a practical option. “Metal free” NaBH4 hydrolysis can also be achieved by the addition of aqueous acids such as hydrochloric acid (HCl) to solid NaBH4. This review summarizes the various catalysts which have been reported in the literature for the hydrolysis of NaBH4.

Abstract

This study investigates the esterification of hydrolyzed sea mango (Cerbera odollam) oil using several cationic ion exchange resins. The best resins were selected based on their performance in a preliminary esterification process. The best resins were then subsequently used in the optimization of the process parameters. The esterification parameters studied were reaction temperature (40–160°C), reaction time (0–5 h), molar ratio of oil to methanol (0.5:1 to 1:14), and catalyst loading (1–14 wt%). Among the resins studied, Amberlyst 15 was found to be the most promising catalyst in the esterification of the hydrolyzed sea mango oil. Moderate reaction temperatures, 60–100°C, were found to be adequate in converting the hydrolyzed sea mango oil into esters. Further investigation revealed that the esterification reaction using the cationic ion exchange resins proceeds at a fast rate, whereby fatty acid methyl esters (FAME) yield of over 80% at moderate reaction temperature was achievable in less than 1 h of reaction time. Small amount of catalyst, which is less than 5 wt%, was also found to be sufficient in catalyzing the esterification process to an acceptable yield.

Abstract

Fibre Reinforced Polymers (FRP) have been widely used to strengthened construction structural elements in the last years because of their mechanical pros. However, the durability of these materials is always controversial. In particular, the effect of long-term contact with water on the mechanical properties of FRPs is studied in this research throughout the implementation of accelerated degradation tests. Samples of Carbon FRP and Glass FRP were immersed into supply water, water with salts and surfactants and highly chlorinated water. In all cases, electrical current passing through the samples was also imposed. Tensile tests on pristine and degraded samples were carried out to determine the influence of these aggressive environments on the tensile strength and the Young‘s modulus of the specimens. Finally, superficial (ATR) FT-IR analyses were conducted to assess possible chemical changes in the samples surfaces. Results indicated that the chemical composition of used resins was not modified due to the water exposure. No hydrolysis process took place during testing time on the surface. However, mechanical properties were reduced, especially when samples were exposed to plain supply water, which may be related to the physical degradation caused by moisture intake by diffusion.