Diffusion of tetrafluoromethane in aluminosilicate nanotubes was studied by means of 13C pulsed field gradient (PFG) NMR at 297 K. The measured data allow the estimation of the diffusivity of tetrafluoromethane inside the nanotubes as well as the diffusivity for these molecules undergoing fast exchange between many nanotubes. The results support the assumption about the one-dimensional nature of the tetrafluoromethane diffusion inside nanotubes.

In the modelling of translational motion, the concepts of frequency-dependent (of the angular fluctuations of the velocity field) self-diffusion and the dispersion tensor are commonly used in its characterisation. Both of these parameters are related to velocity autocorrelation. An alternative means of modelling translational motion is via the equilibrium and nonequilibrium fluctuation-dissipation theorem in classical statistical mechanics. This alternative approach provides further insight into the molecular level processes occurring in the system. Here both of these theoretical fluctuation-dissipation approaches are employed to determine expressions for energy dissipation in simple equilibrium systems exhibiting asymptotic and preasymptotic diffusion and dispersion phenomena and also in a nonequilibrium preasymptotic system involving dispersion within and beyond the upper limit of heterogeneity of an isotropic porous medium. As an example the permeability of porous media due to diffusion and dispersion are studied and it is shown how a frequency-dependent permeability can be treated as a phasor.

Ni based superalloys can be welded by diffusion bonding. Temperature, diffusion coefficient, activation energy and Boltzmann constant influence the quality of diffusion bonding, so obtaining the best condition for welding is considered. Showing the suitable condition for diffusion welding of nickel-based superalloys is the aim of this paper.

The LDD model was first applied to Arsenic concentration profiles determined in surface diffusion experiments by Yoshida and Arai [1]. The new method presented is based on a mathematical convolution with a delta-function-like concentration profile. By comparing the LDD approximation of post-surface diffusion with post-implant diffusion experiments, the same LDD model parameter r is found to hold for both experimental arrangements. This work found that post-implant diffusivity is concentration dependant and this might indicate an anomalous diffusion mechanism for Arsenic.

The solvent resistance properties of the unsaturated polyster and their montmorillonite filled nanocomposites are studied in acetic through equilibrium swelling method at different temperatures. The kinetics of sorption is studied by using the equation of transport phenomena. The values of ‘n’ in solvent transport equation are found to be below ‘0.5’, showing the non-Fickian or pseudo-Fickian transport in the polymer. The dependence of diffusion coefficient on composition and temperature has been studied for all polymeric samples. The diffusion coefficient of unsaturated polyester samples decreases with an increase in unsaturated acid content. The nanocomposite samples show low diffusion coefficient than corresponding pristine polymers. The diffusion coefficient, sorption coefficient and permeation coefficient increase with an increase in temperature for all samples. The crosslink density for neat polymer with varied unsaturated acid content ranges from 2.98 to 3.52 ×105mol/cm3. For the nanocomposite samples it ranges from 3.70 to 5.72 × 105 mol/cm3.

A method has been developed in order to assess small volume interdiffusion coeffcients from experimental Electron Probe MicroAnalysis concentration profiles of polycrystalline materials by means of Boltzmann-Matano or den Broeder methods and their complementary Hall method. These methods have been used as tools for the investigation of the quasi-binary UO2/U(1-y)PuyO(2-z) interdiffusion, for which obtaining a solid solution in the bulk of grains is of major interest. In this paper uncertainties on the interdiffusion coefficient as a function of concentration have been computed for each method. Small volume cofficient measurements were enhanced by means of a small angle acquisition profile line with respect to the interdiffusion interface.

Variation of vacancy formation energy with the parameter of Ashcroft\'s model for nine different exchange and correlation functions show almost similar nature for the bcc metals like Cr, Mo, W, V, Nb, Ta, Tl, Eu and Zr. The mean value of this parameter for these bcc metals are respectively 1.173, 1.383, 1.458, 1.263, 1.478, 1.489, 1.802, 2.222 atomic unit.

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