Efficient and Selective Uptake of TcO4– by a Cationic Metal–Organic Framework Material with Open Ag+ Sites

化学 离子交换 吸附 水溶液 阳离子聚合 金属有机骨架 核裂变产物 无机化学 吸附剂 配体(生物化学) 吸附 结晶度 裂变产物 离子 放射化学 结晶学 有机化学 生物化学 受体
作者
Daopeng Sheng,Lin Zhu,Chao Xu,Chengliang Xiao,Yanlong Wang,Yaxing Wang,Lanhua Chen,Juan Diwu,Jing Chen,Zhifang Chai,Thomas E. Albrecht‐Schmitt,Shuao Wang
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:51 (6): 3471-3479 被引量:397
标识
DOI:10.1021/acs.est.7b00339
摘要

99Tc is one of the most problematic radioisotopes in used nuclear fuel owing to its combined features of high fission yield, long half-life, and high environmental mobility. There are only a handful of functional materials that can remove TcO4- anion from aqueous solution and identifying for new, stable materials with high anion-exchange capacities, fast kinetics, and good selectivity remains a challenge. We report here an 8-fold interpenetrated three-dimensional cationic metal-organic framework material, SCU-100, which is assembled from a tetradentate neutral nitrogen-donor ligand and two-coordinate Ag+ cations as potential open metal sites. The structure also contains a series of 1D channels filled with unbound nitrate anions. SCU-100 maintains its crystallinity in aqueous solution over a wide pH range from 1 to 13 and exhibits excellent β and γ radiation-resistance. Initial anion exchange studies show that SCU-100 is able to both quantitatively and rapidly remove TcO4- from water within 30 min. The exchange capacity for the surrogate ReO4- reaches up to 541 mg/g and the distribution coefficient Kd is up to 1.9 × 105 mL/g, which are significantly higher than all previously tested inorganic anion sorbent materials. More importantly, SCU-100 can selectively capture TcO4- in the presence of large excess of competitive anions (NO3-, SO42-, CO32-, and PO43-) and remove as much as 87% of TcO4- from the Hanford low-level waste melter off-gas scrubber simulant stream within 2 h. The sorption mechanism is well elucidated by single crystal X-ray diffraction, showing that the sorbed ReO4- anion is able to selectively coordinate to the open Ag+ sites forming Ag-O-Re bonds and a series of hydrogen bonds. This further leads to a single-crystal-to-single-crystal transformation from an 8-fold interpenetrated framework with disordered nitrate anions to a 4-fold interpenetrated framework with fully ordered ReO4- anions. This work represents a practical case of TcO4- removal by a MOF material and demonstrates the promise of using this type of material as a scavenger for treating anionic radioactive contaminants during the nuclear waste partitioning and remediation processes.
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