Non-evaporable getters (NEGs) are metallic compounds of the IV group, particularly titanium and/or zirconium-based alloys and are usually used as pumps in vacuum technologies since they are able to sorb, by chemical reactions, most of the active gas molecules, with particular efficacy towards hydrogen isotopes. This work suggests an alternative application of these materials to fusion nuclear reactors, where there is the need to recover small amount of tritium from the large helium flow rate composing the primary coolant loop. Starting from the tritium mass balance inside the primary coolant loop, the amount of coolant to be routed inside the coolant purification system (CPS) is identified. Then a feasibility study, based on the bulk getter theory, is presented by considering three different commercial alloys, named ST707, ST101 and ZAO. The results provide the mass, the area and the regeneration parameters of the three different alloys necessary to fulfill the requirements of the CPS unit. By comparing the features of the three alloys, the ZAO material appears the most promising for the proposed application because it requires the lower amount of material and a lower number of regeneration cycles.
This paper reviews the membrane processes for the nuclear fusion fuel cycle—namely, the treatment of the plasma exhaust gases and the extraction of tritium from the breeding blankets. With respect to the traditional processes, the application of membrane reactors to the fusion fuel cycle reduces the tritium inventory and processing time, thus increasing the safety and availability of the system. As an example, self-supported Pd-alloy membrane tubes have been studied for the separation of hydrogen and its isotopes from both gas- and liquid-tritiated streams through water-gas shift and isotopic swamping reactions. Furthermore, this paper describes an innovative membrane system (Membrane Gas–Liquid Contactor) for the extraction of hydrogen isotopes from liquid LiPb blankets. Porous membranes are exposed to the liquid metal that penetrates the pores without passing through them, then realizing a gas–liquid interface through which the mass transfer of hydrogen isotopes takes place. Compared to the conventional hydrogen isotope extraction processes from LiPb that use the “permeator against vacuum” concept, the proposed process significantly reduces mass-transfer resistance by improving the efficiency of the tritium recovery system.
1 October 2010 in International Journal of Hydrogen Energy
Olive mill wastewater (OMW) presents high environmental impact due to the fact of its elevated organic load and toxicity, especially in Mediterranean countries. Its valorization for simultaneous pollutants degradation and green energy production is receiving great attention, mainly via steam reforming for hydrogen generation. Following previous works, the present research goes into detail about OMW valorization, particularly investigating for the first time the potential benefits of OMW–bioethanol mixtures co-reforming for ultra-pure hydrogen production in Pd-membrane reactors. In this manner, the typical large dilution of OMW and, hence, excess water can be used as a reactant for obtaining additional hydrogen from ethanol. Fresh OMW was previously conditioned by filtration and distillation processes, analyzing later the effect of pressure (1–5 bar), oxidizing conditions (N2 or air as carrier gas), gas hourly space velocity (150–1500 h−1), and alcohol concentration on the co-reforming process (5–10% v/v). In all cases, the exploitation of OMW as a source of environmentally friendly hydrogen was demonstrated, obtaining up to 30 NmL·min−1 of pure H2 at the most favorable experimental conditions. In the membrane reactor, higher pressures up to 5 bar promoted both total H2 production and pure H2 recovery due to the increase in the permeate flux despite the negative effect on reforming thermodynamics. The increase of ethanol concentration also provoked a positive effect, although not in a proportional relation. Thus, a greater effect was obtained for the increase from 5% to 7.5% v/v in comparison to the additional improvement up to 10% v/v. On the contrary, the use of oxidative conditions slightly decreased the hydrogen production rate, while the effect of gas hourly space velocity needs to be carefully analyzed due to the contrary effect on potential total H2 generation and pure H2 recovery.