journal article·2024-03-26

Leveraging Hard–Soft Acid–Base Interactions for Effective Palladium Capture in Acidic Solutions

Anastasia D. Pournara, Jun-Hao Tang, Lu Yang, Jia-Ting Liu, Xiao-Ying Huang, Mei-Ling Feng, Mercouri G. Kanatzidis

Chemistry of Materials· Volume 36· Issue 6
Publisher page

Abstract

Demand for palladium is increasing as it is a precious metal with great industrial applications. In order to meet the potential challenges posed by limited terrestrial Pd resources, it is necessary to develop low-cost and efficient Pd enrichment materials and methods. Palladium is found in significant quantities in spent fuel as a fission product, making it highly valuable for recycling. However, the selective capture of Pd 2+ ions from highly acidic radioactive liquid wastes, with complex compositions generated from spent fuel reprocessing, remains a challenge. Leveraging the intrinsic bonding selectivities associated with hard–soft acid–base (HSAB) theory we present, the rapid and highly selective capture of Pd 2+ ions from strongly acidic solutions has been achieved by the layered potassium thiostannate K 2 x Sn 4– x S 8– x ( KTS-3 ). The maximum sorption capacity was calculated to be 397 and 162 mg of Pd 2+ /g of KTS-3 in 1 and 3 M HNO 3 solutions, respectively. In 1 M HNO 3 solutions with initial Pd 2+ concentrations of 1.02 and 260 mg/L, the sorption of Pd 2+ by KTS-3 reaches equilibrium within 2 and 30 min, respectively, with removal rates of more than 99.9%. KTS-3 can effectively and selectively remove Pd 2+ from mixtures containing Ag + or Pt 2+, although they also represent soft Lewis acids and pose strong competition with Pd 2+ for binding to the soft base S 2– sites of the framework. Moreover, KTS-3 can effectively separate Pd 2+ /M n + (M n + = Na +, Cs +, Sr 2+, Eu 3+, Zr 4+, Ni 2+, and Co 2+ ) in acidic solutions and shows excellent selective capture of Pd 2+ even in simulated high-level liquid wastes. The outstanding Pd 2+ sorption by KTS-3, showcasing a record-breaking capacity and selectivity, is attributed to the synergistic effect of the easily exchangeable K + cations and the strong HSAB affinity of the S 2– active sites for Pd 2+ ions. This is achieved under extremely acidic conditions, which coupled with its structural integrity and effectiveness even post γ-irradiation, positions it as a promising material for palladium capture and recovery, especially in the treatment of radioactive waste.
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Research context

OpenAlex topics: Radioactive element chemistry and processing · Chemical Synthesis and Characterization · Extraction and Separation Processes

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Affiliations

Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P.R. China

University of Chinese Academy of Sciences, Beijing 100049, P.R. China

Fujian Province Joint Innovation Key Laboratory of Fuel and Materials in Clean Nuclear Energy System, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, P.R. China

References (49)

Show source-provided references
1. 10.1038/nature1100810.1038/nature11008 ↗
2. 10.1126/science.aac615310.1126/science.aac6153 ↗
3. 10.1039/C6TA07050G10.1039/C6TA07050G ↗
4. 10.1016/S1369-7021(11)70143-210.1016/S1369-7021(11)70143-2 ↗
5. 10.1021/acsaem.2c0031710.1021/acsaem.2c00317 ↗
6. 10.1002/adma.20200592910.1002/adma.202005929 ↗
7. 10.1595/003214003X472748710.1595/003214003X4727487 ↗
8. 10.1039/C8TA09849B10.1039/C8TA09849B ↗
9. 10.1023/B:JRNC.0000034890.23325.b510.1023/B:JRNC.0000034890.23325.b5 ↗
10. 10.1515/ract-2020-007110.1515/ract-2020-0071 ↗
11. 10.1002/adsc.20040407110.1002/adsc.200404071 ↗
12. 10.1023/B:JRNC.0000034890.23325.b510.1023/B:JRNC.0000034890.23325.b5 ↗
13. 10.1080/01496395.2012.70773210.1080/01496395.2012.707732 ↗
14. 10.1016/j.cej.2018.05.13010.1016/j.cej.2018.05.130 ↗
15. 10.1021/acsanm.0c0022710.1021/acsanm.0c00227 ↗
16. 10.1016/S0304-386X(02)00194-910.1016/S0304-386X(02)00194-9 ↗
17. 10.1016/j.hydromet.2010.03.01310.1016/j.hydromet.2010.03.013 ↗
18. 10.1016/0376-7388(96)00102-010.1016/0376-7388(96)00102-0 ↗
19. 10.1039/C6SC01039C10.1039/C6SC01039C ↗
20. 10.1016/S0304-3894(02)00263-710.1016/S0304-3894(02)00263-7 ↗
21. 10.1039/C4TA06678B10.1039/C4TA06678B ↗
22. 10.1002/smll.20180524210.1002/smll.201805242 ↗
23. 10.1016/j.chempr.2022.02.01610.1016/j.chempr.2022.02.016 ↗
24. 10.1007/s11426-022-1484-010.1007/s11426-022-1484-0 ↗
25. 10.1098/rsos.17170110.1098/rsos.171701 ↗
26. 10.1016/j.jhazmat.2008.09.05310.1016/j.jhazmat.2008.09.053 ↗
27. 10.1016/j.jhazmat.2008.02.01710.1016/j.jhazmat.2008.02.017 ↗
28. 10.1016/j.cej.2013.07.11610.1016/j.cej.2013.07.116 ↗
29. 10.1016/j.cej.2018.10.01010.1016/j.cej.2018.10.010 ↗
30. 10.14102/j.cnki.0254-5861.2011-301810.14102/j.cnki.0254-5861.2011-3018 ↗
31. 10.1021/ja900977p10.1021/ja900977p ↗
32. 10.1021/cm400699r10.1021/cm400699r ↗
33. 10.1039/C5TA00566C10.1039/C5TA00566C ↗
34. 10.1021/jacs.6b0735110.1021/jacs.6b07351 ↗
35. 10.1021/jacs.7b0056510.1021/jacs.7b00565 ↗
36. 10.1021/jacs.8b0745710.1021/jacs.8b07457 ↗
37. 10.1016/j.cej.2019.05.07010.1016/j.cej.2019.05.070 ↗
38. 10.1021/acs.inorgchem.3c0206410.1021/acs.inorgchem.3c02064 ↗
39. 10.1039/C5SC03040D10.1039/C5SC03040D ↗
40. 10.1007/BF0270834010.1007/BF02708340 ↗
41. 10.1063/1.219688210.1063/1.2196882 ↗
42. 10.1021/ja00134a02110.1021/ja00134a021 ↗
43. 10.1039/C6TA06404C10.1039/C6TA06404C ↗
44. 10.1016/j.cej.2016.04.07910.1016/j.cej.2016.04.079 ↗
45. 10.1016/S0032-9592(98)00112-510.1016/S0032-9592(98)00112-5 ↗
46. 10.1038/s41467-022-28217-810.1038/s41467-022-28217-8 ↗
47. 10.1039/C9GC00166B10.1039/C9GC00166B ↗
48. 10.1016/j.jece.2021.10696610.1016/j.jece.2021.106966 ↗
49. 10.1016/0301-4622(94)00051-410.1016/0301-4622(94)00051-4 ↗