“…These values were then fitted using an Arrhenius-type equation with a correlation factor R 2 = 0.981, P • E of 3.39 × 10 −8 mol s −1 m −1 Pa −0.5 and E A of 5154 J mol −1 . The permeability and E A values are in agreement with those reported in the literature for similar Pd-Ag membranes [33,43].…”
“…These values were then fitted using an Arrhenius-type equation with a correlation factor R 2 = 0.981, P • E of 3.39 × 10 −8 mol s −1 m −1 Pa −0.5 and E A of 5154 J mol −1 . The permeability and E A values are in agreement with those reported in the literature for similar Pd-Ag membranes [33,43].…”
“…All these techniques require dedicated set-ups and non-trivial procedures [18]. Quite recently, a series of non-ideal behaviours were considered and reformulations of the Fick's law were suggested and applied to experimental data [19][20][21]. Moreover, some first principle calculations were performed in order to calculate the diffusion coefficient in a large variety of metals [22].…”
A large number of metallic alloys are currently under investigation in the field of hydrogen storage and hydrogen separation membranes. For such applications, the knowledge of the hydrogen diffusion coefficient in the given alloy is of great importance even if its direct measurement is not always easy to perform. In this view, the aim of this work is to describe an innovative procedure able to provide the lower limit of the hydrogen diffusion coefficient by performing hydrogen absorption kinetic experiments. Two different tools are presented: The first is a numerical code which solves the diffusion problem inside metals according to the general theory of the transport phenomena, and the second is a dimensional analysis that describes the dependence of the hydrogen diffusion coefficient from a few governing parameters. Starting from the results of several hydrogen absorption kinetic experiments performed on a Pd–Ag sample under different experimental conditions, the hydrogen diffusion coefficients were assessed by using both the described tools. A good agreement among the results obtained by means of the two procedures was observed.
“…The results obtained with a H 2 O/Ethanol molar ratio of 10 suggest that part of the water excess dilutes the hydrogen produced in the reaction zone resulting in a lower hydrogen partial pressure difference between both sides of the membrane. Tosti et al [20] reported that an excess of a limiting reagent increases the reaction conversion in a traditional reactor. However, in a membrane reactor such an excess reduces the partial pressure of the permeating species (hydrogen) and as a consequence, the shift effect of the membrane is depressed.…”
Section: Comparison Between Rh-based Catalystsmentioning
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