The rate of vapor-phase sorption of tetrahydrofuran (THF), tetrahydropyran (THP), and 1,4-dioxan (DIOX) onto a Wyoming montmorillonite saturated with Al3+ or Cr3+ has been studied by isothermal gravimetry in the temperature range 18° to 105°C using samples of different weights and grain-size distributions. The rate of sorption for all the cyclic ethers increased with decreasing sample and grain size, demonstrating that inter-, rather than intraparticle mass transfer was rate-determining. Optimization of the sample parameters (2 mg sample of <45-μm grain size, pretreated at 120°C yielded integral diffusion coefficients at 18°C of 0.5 × 10−14 m2/s for DIOX for the Cr3+-clay to 3.5 × 10−4 m2/s for THF for the Al3+-clay; however, no temperature or cationic dependence of the cyclic ether uptake was observed. In general, the rate of sorption of the cyclic ethers increased as THF ≥ THP > DIOX indicating that the sorption rate of THF and THP was dependent on concentration or that DIOX sorption was retarded by bidentate coordination to aluminum ions at the edges of the clay platelets.

For a better understanding of the physical phenomena associated with the appearance of defects in laser welding, a heat and fluid flow model is developed using Comsol Multiphysics®. This first step of the project is focused on the modeling of a static laser shot on a sample of steel. This 2D axially-symmetric configuration is used to study the main physical phenomena related to the creation of the keyhole. This model takes into account the three phases of the matter: the vaporized metal, the liquid phase and the solid base. To track the evolution of these three phases, coupled equations of energy and momentum are solved. The liquid/vapor interface is tracked using the Level-Set method. The calculated velocity and free surface deformation are analyzed. Melt pool shapes are compared with experimental macrographs and the influence of some parameters such as laser power is discussed.