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熔盐助熔剂法生长碱金属铀酰硼酸盐晶体:A(UO₂)BO₃(A = Cs、Rb、K)的表征及离子交换行为

Crystal Growth of Alkali Uranyl Borates from Molten Salt Fluxes: Characterization and Ion Exchange Behavior of A(UO)BO (A = Cs, Rb, K).

作者信息

Pace Kristen A, Koch Robert J, Smith Mark D, Morrison Gregory, Klepov Vladislav V, Besmann Theodore M, Misture Scott T, Zur Loye Hans-Conrad

机构信息

Center for Hierarchical Waste form Materials, Columbia, South Carolina 29208, United States.

Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, United States.

出版信息

Inorg Chem. 2020 May 4;59(9):6449-6459. doi: 10.1021/acs.inorgchem.0c00536. Epub 2020 Apr 10.

Abstract

A new family of layered alkali uranyl borates, A(UO)BO (A = Cs, Rb, K), was synthesized as high quality single crystals via high temperature flux growth methods. At room temperature, the compounds are structurally closely related although they crystallize in different monoclinic space groups, specifically 2/ (Cs), 2/ (Rb), and 2/ (K). At a low temperature (100 K), Cs(UO)BO becomes isostructural with K(UO)BO as the result of a reversible structure transition by Cs(UO)BO. The title phases represent the first examples of uranyl borates resulting from high temperature flux growth utilizing alkali halide fluxes. The synthesis, structures, and thermal, optical, and ion exchange properties are reported, and modeling of the atomic structure and disorder of the ion exchanged phases is discussed.

摘要

通过高温助熔剂生长法合成了一个新的层状碱金属铀酰硼酸盐系列,即A(UO₂)BO₃(A = Cs、Rb、K),并生长出了高质量的单晶。在室温下,这些化合物在结构上密切相关,尽管它们结晶于不同的单斜空间群,具体为C2/m(Cs)、C2/m(Rb)和C2/m(K)。在低温(100 K)下,Cs(UO₂)BO₃通过可逆结构转变与K(UO₂)BO₃成为同构体。这些标题相代表了利用碱金属卤化物助熔剂通过高温助熔剂生长得到的铀酰硼酸盐的首个实例。本文报道了其合成、结构以及热学、光学和离子交换性质,并讨论了离子交换相的原子结构和无序性建模。

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