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Efficient removal of iodide (I−) and iodate (IO3−) from aqueous solution is highly desirable for waste disposal and remediation of radioiodine contamination. We report here a bifunctional anion exchange resin Purolite A530E for the effective I−/IO3− adsorption, which shows a priority anion-exchange affinity for I− (99%) over IO3− (9.7%). The maximum adsorption capacity for I− is 275.16 mg·g−1 fitted by the Langmuir isotherm model, much higher than most adsorbents. Furthermore, Purolite A530E exhibits great selectivity for I− over competing anions, which endows the resin with promising I− remediation that over 99% I− can be removed from simulated Hanford groundwater (HGW). [ABSTRACT FROM AUTHOR]

Crystalline solids of zeolitic imidazolate framework (ZIF)-69 with a suitable pore window size matching with atomic diameter of xenon is utilized for this task, showing notable performance for Xe/Kr capture and separation as well as decent hydrolytic and irradiation stabilities. The results illustrate that the saturated uptake amount of Xe by ZIF-69 is 2.46 mmol/g at 298 K, while Kr uptake is only 0.55 mmol/g. Importantly, the separation ratio of Xe/Kr is 8.35, one of the highest values among all solid sorbent material reported up to now. These findings suggest that ZIF-69 is a potential candidate for the application of xenon capture and purification form a gas mixture containing Kr. [ABSTRACT FROM AUTHOR]

This study highlights the simultaneous sequestration of U(VI) and arsenate at the goethite/water interface. The uptake trends and speciation of these two components were related with molar arsenate/U(VI) ratio, solution pH, contact order and aging time. A metastable [UO(HAsO)·HO] was observed after 3 days and then this solid completely transformed into Na(UOAsO)·3HO after 7 days. The disodium ethylenediamine tetraacetate ligand gave rise to the complete dissolution of Na(UOAsO)·3HO phase and the release of U(VI) and arsenate back into the solution. The experimental findings facilitated us better comprehend the migration and fate of coexisting U(VI) and arsenate in the aquatic environment. [ABSTRACT FROM AUTHOR]

In the original publication of the article, Fig. 8 was erroneously plotted due to unintentional misoperation of batch input of the XRD data which caused the repeating patterns of Single-U5 and Single-U50 in this figure. [ABSTRACT FROM AUTHOR]