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Study on molten salt oxidation process of simulated Co doped cation exchange resins.

Authors :
Xue, Yun
Wang, Yue-Lin
Li, Yu
Xu, Wen-Da
Ma, Fu-Qiu
Zheng, Yang-Hai
Zhang, Qing-Guo
Zhang, Zhi
Zhang, Mi-Lin
Yan, Yong-De
Source :
Journal of Industrial & Engineering Chemistry; Oct2023, Vol. 126, p398-407, 10p
Publication Year :
2023

Abstract

Cation exchange resins (CERs) are widely applied to purify waste liquids generated during the operation of nuclear reactors. The radioactive nuclides <superscript>60</superscript>Co and <superscript>58</superscript>Co are important corrosion activation products in reactor cooling water. In this study, the simulated Co doped CERs were oxidized with ternary carbonate. According to the thermogravimetric analysis (TG), the decomposition of Co doped CERs includes three processes: 1. Elimination of the osmotic water; 2. Pyrolysis of sulfonic acid group; 3. Destruction of styrene–divinylbenzene copolymer. The X-Ray Diffraction (XRD) patterns indicate that sulfur mainly exists in the form of sulfate in waste salt. The Co<superscript>2+</superscript> undergoes the path of CoS 2 → Co 3 O 4 with the increase of temperature and the transition point is 650 °C. Combined with Fourier Transform Infrared Spectrometer (FT-IR) spectra and X-ray Photoelectron Spectroscopy (XPS) analysis, sulfonic acid groups begin to decompose at 350 °C. During the molten salt oxidation process, most of the sulfur in sulfonic acid groups is entrapped by carbonate as the form of sulfate, and a little of which remains as sulfone group, sulfoxide group and sulfur bridge in residue. When the resins are oxidized at 800 °C, the retention rate of Co<superscript>2+</superscript> is 97.3%, indicating that the molten salt oxidation can effectively remain Co<superscript>2+</superscript> and convert it into a more stable substance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1226086X
Volume :
126
Database :
Supplemental Index
Journal :
Journal of Industrial & Engineering Chemistry
Publication Type :
Periodical
Accession number :
164963475
Full Text :
https://doi.org/10.1016/j.jiec.2023.06.028