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  1. 原著論文

Pebble structure change of Li2TiO3 with excess Li in water vapor atmosphere at elevated temperatures

https://repo.qst.go.jp/records/48275
https://repo.qst.go.jp/records/48275
26e832ee-d95c-4ee4-b43e-994dfd453cce
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-08-07
タイトル
タイトル Pebble structure change of Li2TiO3 with excess Li in water vapor atmosphere at elevated temperatures
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Katayama, K.

× Katayama, K.

WEKO 485157

Katayama, K.

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Shimozori, M.

× Shimozori, M.

WEKO 485158

Shimozori, M.

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星野, 毅

× 星野, 毅

WEKO 485159

星野, 毅

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Yamamoto, R.

× Yamamoto, R.

WEKO 485160

Yamamoto, R.

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Ushida, H.

× Ushida, H.

WEKO 485161

Ushida, H.

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Fukada, S.

× Fukada, S.

WEKO 485162

Fukada, S.

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星野 毅

× 星野 毅

WEKO 485163

en 星野 毅

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抄録
内容記述タイプ Abstract
内容記述 The pebbles of Li2TiO3 with excess Li, which is in a developmental stage in JAEA (Japan Atomic Energy Agency) as an advanced tritium breeding material, were exposed to water vapor at elevated temperatures. In the temperature rising process from room temperature to 900 °C, pore distribution and BET surface area were largely changed. The surface area decreased gradually by a sintering effect when maintained at 900 °C for a long time. The release of water vapor was observed at about 450 °C by the decomposition of LiOH in addition to the release of adsorbed water at the beginning of heating. A large release peak of CO2 was observed at 700 °C. This is caused by the decomposition of Li2CO3. A remarkable melt layer was formed on the pebble surface over 700 °C by melting of Li2CO3. The change of pebble structure and the influences of LiOH and Li2CO3 have to be taken into account, when the release behavior of bred tritium from Li2TiO3 pebbles is discussed.
書誌情報 Nuclear Materials and Energy

巻 9, p. 242-246, 発行日 2016-12
出版者
出版者 ELSEVIER
ISSN
収録物識別子タイプ ISSN
収録物識別子 0022-3115
DOI
識別子タイプ DOI
関連識別子 10.1016/j.nme.2016.05.006
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