日本地球惑星科学連合2016年大会

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セッション記号 M (領域外・複数領域) » M-IS ジョイント

[M-IS12] 結晶成長、溶解における界面・ナノ現象

2016年5月22日(日) 09:00 〜 10:30 A07 (アパホテル&リゾート 東京ベイ幕張)

コンビーナ:*木村 勇気(北海道大学低温科学研究所)、三浦 均(名古屋市立大学大学院システム自然科学研究科)、塚本 勝男(大阪大学大学院工学研究科)、佐藤 久夫(三菱マテリアル株式会社エネルギー事業センター那珂エネルギー開発研究所)、座長:佐藤 久夫(三菱マテリアル株式会社エネルギー事業センター那珂エネルギー開発研究所)

09:30 〜 09:45

[MIS12-02] 固液界面の原子スケール観察によるモンモリロナイトのイオン交換に対する水和構造依存性の解明

*荒木 優希1佐藤 久夫2大西 洋1 (1.神戸大学大学院理学研究科、2.三菱マテリアル)

キーワード:粘土鉱物、イオン交換、水和、周波数変調方式原子間力顕微鏡

Cations of clay mineral are exchangeable depending on the atomic weight and electric density. Because of this ion exchange property, the clays are expected to capture the radionuclide which is diffused in the soil. Recently, the effect of water molecules on the ion exchange tendency has been suggested (S. Charles et al., 2006). In order to clarify the behavior of the water molecules at the clay-solution interface, we conducted the atomic-scale observation of the hydration structure in the vicinity of the montmorillonite surfaces in several ionic solutions.The frequency modulation atomic force microscopy (FM-AFM) which was modified based on the commercial AFM (SPM-9600, Shimadzu Corp., Japan) was employed for the atomic scale observation of interfacial structure (T. Fukuma et al., 2005). This FM-AFM technique has achieved the visualization of the 2D or 3D density map of the water molecules in the vicinity of crystal surfaces (K. Kimura et al., 2010; T. Fukuma et al., 2010). We observed the natural montmorillonite surfaces by FM-AFM in the 0.1 M KCl, CsCl, CaCl2 solutions, respectively. The 100 nm plate-like particles of the montmorillonite were fixed on the mica substrate surfaces, then the (001) face and the interface were observed (Fig.1).The upper images in Fig.1 show the topography of the montmorillonite surfaces. The protrusions (brighter areas) indicate the cation sites of the montmroillonite surfaces which were located in the center of the six-membered rings of silicate tetrahedra. The interface of the montmorillonite and the solutions were observed along the dashed line in the upper images (bottom images in Fig.1). The bottom images showed the three brighter layers presented by arrows. These brighter areas indicate the distribution of the hydrated water molecules.Our results revealed that the hydration structure in the vicinity of the montmorillonite surfaces is uniform regardless of the cations in the solutions. It is suggested that the water molecules around the surface would not affect the ion exchange at the clay surfaces.