No abstract

Present results are relevant for the calculation on the partial pressure of oxygen, available at different depths into the corneal tissue behind contact lenses of different oxygen transmissibility.

In this work we study the diffusion–adsorption process in porous media and analyze the effect that the irregular geometry of the pores has on the efficiency of two types of adsorption processes: (a) when there is a net flux along the pore and (b) when the pore is completely saturated. In the first case, we measured the mass transfer coefficient, which is the constant of proportionality between the net flux and the difference of concentration. In the second case, we measure the effectiveness factor, which is the ratio between the actual rate of adsorption and the rate which would be achieved if the entire surface were at the same external concentration. In order to perform this analysis, we use a generalized Fick–Jacobs equation that considers the net effect of diffusion and adsorption along the direction of transport. For this analysis we have used wedge-shaped and conical pores, due to the simplicity of the treatment and their importance in the elaboration of a new brand of artificial materials. We have proved that the enhancement or diminution of the mass transfer coefficient or the effectiveness factor depend upon the specific rate of adsorption; therefore, they can be controlled using our model as a prediction tool in order to build artificial materials with a specific output flux of material. Additionally, our work allows to find how the Thiele modulus locally depends on the geometry of the pore for a linear reaction.

The transport properties of mixed salts based on CsH2PO4 are influenced by the interactions among charge carriers.

This article describes the diffusion and permeability of oxygen, carbon dioxide, methane, ethane, ethylene, propane, and propylene in 1‐octene based polyethylene of densities 0.94, 0.92, 0.904, and 0.87. The isotherms obtained in the time‐lag experimental device display a diffusion coefficient and permeability behavior similar to that of glassy polymers. We apply the dual model to semicrystalline polymers assuming that Henry's sites are related to the amorphous phase, which decreases when the crystallinity percentage increases. Whereas the interphase of the polymeric matrix and the crystalline phase prevails and acts as Langmuir sites. Their effect is to increase both, the tortuosity of diffusion trajectories and the chain immobilization. We now explain this effect using thermodynamic considerations. In fact, the tortuosity is related to the change in activation entropy, and the chain immobilization to the cohesive energy of the polymeric matrix. In those terms, the diffusion coefficient does not follow the same crystalline percentage dependence than the solubility. According to the previous findings, the solubility changes in proportion to amorphous percentages. Instead, diffusion coefficient has exponential dependence. Furthermore, we show that the permeability changes as a consequence of the modification of diffusion and solubility, according to the product of both quantities. Comparison with previous publication has been included. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 634–642, 2010