“…Ideally, pore diffusion coefficients can be derived from batch kinetics distribution studies where the mass transfer resistance associated with film diffusion is minimized through significant mechanical mixing (note that, mixing techniques must be limited such that physical grinding of the particles does not become excessive). A time-dependent technetium distribution study was performed in simulated DSSF waste by Kurath et al, 1999. Batch kinetics tests, where inadequate mixing is achieved between the solid and solution, result in overall diffusion coefficients that are in effect smaller than the actual pore diffusion coefficient. Therefore, the use of the batch kinetics data taken by Kurath et al (1999) can provide us with a lower bound estimate of pore diffusion, while molecular diffusion becomes our upper bound.…”