JpGU-AGU Joint Meeting 2020

講演情報

[J] 口頭発表

セッション記号 M (領域外・複数領域) » M-IS ジョイント

[M-IS23] 結晶成⻑、溶解における界⾯・ナノ現象

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)、佐藤 久夫(日本原燃株式会社埋設事業部)

[MIS23-08] ノルセサイトの結晶化機構の統一的理解

*麻川 明俊1畝田 廣志1磯部 馨1越後 至1菅 光希1小松 隆一1 (1.山口大学大学院創成科学研究科)

キーワード:ノルセサイト、溶液媒介相転移

Norsethite BaMg(CO3)2 has the space group of R32, and shows strong asymmetry. Hence, norsethite exhibits the high birefringence (norsethite:0.175; quartz:0.009), and expect that norsethite can be utilized as new piezoelectric crystals. Furthermore, norsethite is one of the dolomite analogue (space group of dolomite CaMg(CO3)2:R3-), and attracts much attention as the model material to clarify the dolomite issue. Here, we demonstrate the norsethite crystallization mechanism under atmospheric pressure. By the comparison of nucleation kinetics between norsethite and barium carbonate, we revealed that norsethite is apparently formed from barium carbonate by the solution-mediated transformation. In contrast, when the dissolution enthalpy and entropy were obtained from the van’t Hoff plots of norsethite and barium carbonate, respectively, we revealed that norsethite co-precipitate with barium carbonate at less than 80 °C, and norsethite emerge by the solution-mediated transformation over 80 °C. We concluded that it is essential to analyze both the thermodynamic stability and the nucleation kinetics for the understanding of the norsethite crystallization mechanism.