Structure, tritium depth profile and desorption from ‘plasma-facing’ beryllium materials of ITER-Like-Wall at JET

•In ILW limiter beryllium tiles more than 95% of tritium is accumulated in the first 30–45m from the ‘plasma-facing’ surface, however, possible presence of tritium in low concentration up to the depth of 100m cannot be excluded.•Highest tritium concentration can be found in the outer wall region of...

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Bibliographic Details
Published in:Nuclear materials and energy 2017-08, Vol.12, p.642-647
Main Authors: Pajuste, E., Kizane, G., Vitins, A., Igaune, I., Avotina, L., Zarins, R.
Format: Article
Language:eng
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Summary:•In ILW limiter beryllium tiles more than 95% of tritium is accumulated in the first 30–45m from the ‘plasma-facing’ surface, however, possible presence of tritium in low concentration up to the depth of 100m cannot be excluded.•Highest tritium concentration can be found in the outer wall region of the vacuum vessel.•The degree of detritiation of samples from beryllium tiles > 91% can be obtained upon reaching 1075K.•Erosion and melting of the beryllium can be observed in the central parts of the tiles, whereas side parts are mostly covered by the deposition layers. Tritium depth profile and its temperature programmed desorption rate were determined for selected samples cut out of beryllium tiles removed from the Joint European Torus vacuum vessel during the 2012 shut down. A beryllium dissolution method under controlled conditions was used to determine the tritium depth profile in the samples, whereas temperature programmed desorption experiments were performed to assess tritium release pattern. Released tritium was measured using a proportional gas flow detector. Prior to desorption and dissolution experiments, the plasma-facing surfaces of the samples were studied by scanning electron microscopy and energy dispersive X-ray spectroscopy. Experimental results revealed that > 95% of the tritium was localized in the top 30 – 45µm of the ‘plasma-facing’ surface, however, possible tritium presence up to 100µm cannot be excluded. During temperature programmed desorption at 4.8K/min in the flow of purge gas He+ 0.1% H2 the tritium release started below 475K, the most intense release occurred at 725 – 915K and the degree of detritiation of > 91% can be obtained upon reaching 1075K. The total tritium activity in the samples was in range of 2 – 32kilo Becquerel per square centimetre of the plasma-facing surface area.
ISSN:2352-1791
2352-1791