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Tamain, C.*; Bonato, L.*; Aupiais, J.*; Dumas, T.*; Guillaumont, D.*; Barkleit, A.*; Berthon, C.*; Solari, P. L.*; 池田 篤史; Guilbard, P.*; et al.
European Journal of Inorganic Chemistry, 2020(14), p.1331 - 1344, 2020/04
被引用回数:3 パーセンタイル:23.3(Chemistry, Inorganic & Nuclear)水溶液中における三価アメリシウム(Am(III))とクエン酸(Citric acid)の配位・錯形成反応について、可視吸収分光, NMR, X戦吸収分光(EXAFS), TRLFS、及び電気泳動測定を実施し、溶液中に生成している化学種の数、種類、及びその配位・錯形成状態についての検討を行った。当該実験結果はさらに量子化学計算の結果とも組み合わせ、生成化学種の詳細な配位・錯体構造について検討した。
Micheau, C.; 上田 祐生; 元川 竜平; Moussaoui, S.*; Makombe, E.*; Daniel, M.*; Berthon, L.*; Bourgeois, D.*; 阿久津 和宏*
no journal, ,
The DIAMEX process aims to separate minor f-elements using malonamide as extractant molecules such as N,N'-dimethyl-N,N'-dibutyl-tetradecyl-malonamide (DBMA). Recently, Poirot studied the effect of n-heptane and toluene on the selectivity of DBMA between Pd and Nd and have conclude that Pd extraction is driven by coordination whereas Nd extraction is driven by extractant aggregation. More recently, a specific study on tetrahexylmalonamide (THMA) in toluene demonstrated a superior selectivity for Pd compared to DBMA. THMA molecular structure suggests poor aptitude for aggregation compared with DBMA, and has been much less characterized. Supramolecular features of two different solvent extraction systems based on malonamide extractants, THMA in toluene and DBMA in heptane, have been studied using characterization techniques dedicated to bulk organic phase organisation, ie. small angle X-ray scattering, and to interface characterization, ie. neutron reflectivity and interfacial tension.