Author/Authors :
Nakagawa، نويسنده , , S and Matsuyama، نويسنده , , M and Kodama، نويسنده , , H and Oya، نويسنده , , Y and Okuno، نويسنده , , K and Sagara، نويسنده , , A and Noda، نويسنده , , N and Watanabe، نويسنده , , K، نويسنده ,
Abstract :
Release and diffusion behavior of tritium implanted into thin boron films were examined by isochronal and isothermal heating. For comparison, a polycrystal boron plate was also employed for the same examinations. Changes in the residual amount of tritium with heating were measured by β-ray-induced X-ray spectrometry (BIXS). Most of the tritium desorbed at room temperature was in HTO form, and the residual amount decreased to 20–30% of the initial amount loaded at 773 K. The time-course of the tritium reduction was well represented by an exponential function, suggesting that the tritium release obeys first order reaction kinetics and the rate-determining step is a diffusion process. The apparent activation energy of diffusion was determined to be 0.17 eV. Both the depth profiles calculated from a diffusion equation and determined by computer simulation of X-ray spectra agreed quite well for polycrystal boron.