| Literature DB >> 33856787 |
Rongzhen Xie1, Nannan Shen1, Xijian Chen1, Jie Li1, Yaxing Wang1, Chao Zhang2, Chengliang Xiao3, Zhifang Chai1, Shuao Wang1.
Abstract
99Tc is one of the most abundant radiotoxic isotopes in used nuclear fuel with a high fission yield and a long half-life. Effective removal of pertechnetate (TcO4-) from an aqueous solution is important for nuclear waste separation and remediation. Herein, we report a series of facilely obtained benzene-linked guanidiniums that could precipitate TcO4- and its nonradioactive surrogate ReO4- from a high-concentration acidic solution through self-assembly crystallization. The resulting perrhenate and pertechnetate solids exhibit exceptionally low aqueous solubility. The benzene-linked guanidiniums hold one of the highest TcO4- removal capacities (1279 mg g-1) among previously reported materials and possess a removal percentage of 59% for ReO4- in the presence of Cl- over 50 times. The crystallization mechanism was clearly illustrated by the single-crystal structures and density functional theory calculations, indicating that TcO4- is captured through a charge-assisted hydrogen bonding interaction and stabilized by π-π stacking layers. In addition, the removal process is easily recycled and no toxic organic reagents are introduced. This work provides a green approach to preliminarily separate TcO4- from high-level nuclear wastes.Entities:
Year: 2021 PMID: 33856787 DOI: 10.1021/acs.inorgchem.1c00187
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165