Xiao Kexing, Yang Yuqing, Xu Xiaohan, Szymanowski Jennifer E S, Zhou Yifan, Sigmon Ginger E, Burns Peter C, Liu Tianbo
School of Polymer Science and Polymer Engineering, The University of Akron, Akron, Ohio 44325, United States.
Inorg Chem. 2024 Aug 19;63(33):15331-15339. doi: 10.1021/acs.inorgchem.4c02103. Epub 2024 Aug 6.
We report a complex coacervate formed by a 2.5 nm-diameter, rigid uranyl peroxide molecular cluster (LiK(OH))[UO(O)OH], U) and SrCl salt in dilute aqueous solutions, including its location in the phase diagram, composition, rheological features, and critical conditions for phase transitions. In this coacervate, the Sr cations are a major building component, and the coacervate phase covers a substantial region of the phase diagram. This coacervate demonstrates features that differ from traditional coacervates formed by oppositely charged long-chain polyelectrolytes, especially in its formation mechanism, dehydration, enhancement of mechanical strength with increasing ionic strength, and the change of salt partition preference into the coacervate and supernatant phases with ionic strength.
我们报道了一种由直径为2.5纳米的刚性过氧化铀酰分子簇(LiK(OH))[UO(O)OH]、U)和SrCl盐在稀水溶液中形成的复杂凝聚层,包括其在相图中的位置、组成、流变学特征以及相变的临界条件。在这种凝聚层中,Sr阳离子是主要的结构成分,并且凝聚层相覆盖了相图的很大一部分区域。这种凝聚层表现出与由带相反电荷的长链聚电解质形成的传统凝聚层不同的特征,特别是在其形成机制、脱水、随着离子强度增加机械强度增强以及盐在凝聚层和上清液相之间的分配偏好随离子强度的变化方面。