A ceramic BCN target with samples of dense RG-Ti-91 without boron, RG-Ti-B
with boron (0.1 at,%) and porous POGO AXF-5Q graphites was exposed in a sta
tionary D-plasma of the 'Lenta' device with an ion energy of 200 eV and an
ion flux of (3 - 6) x 10(17) D/cm(2)s at 1040 and 1400 K to a fluence of si
milar to 1 x 10(22) D/cm(2), Codeposited layers were obtained for compariso
n on the target surface. Thermal desorption spectroscopy (TDS showed that t
he amount of deuterium in RG-Ti after exposure at 1040 K was more than an o
rder of magnitude higher than in POGO (9 x 10(17) and 7 x 10(16) D/cm(2), r
espectively). The retention took place preferentially in a surface layer ab
out 100 mu m thick. The bulk deuterium concentration in both RG-Ti and POGO
was lower than 1 appm. The irradiated RG-Ti surface was subjected to stron
g erosion and consisted of 'columnar' grains covered with TiC at their tips
. The deuterium in RG-Ti irradiated at 1400 K was located in the surface la
yer (1.5 x 10(16) D/cm(2)), The value of the bulk concentration did not exc
eed 0.1 appm while in POGO it was equal to about 20 appm. TDS for deuterium
in RG-Ti demonstrated a spectrum similar to that for codeposited layers on
a target surface. The differences in deuterium retention in the graphites
are explained on the basis of structural differences. Considering tritium i
nventory assessment for ITER, dense graphites like RG-Ti are preferred for
working divertor plates at high temperatures. (C) 1999 Elsevier Science B.V
. All rights reserved.