Led by Kuk Cho, the researchers designed a novel layered potassium calcium thiostannate (KCaSnS), a calcium (Ca2+)-doped chalcogenide ion exchanger. The process overcomes the difficulty in removing cesium-137 from acidic wastewater, where protons (H+) impair the adsorption ability and damage the lattice structure of the adsorbent.
The study, titled “Leaching of structural Ca2+ ions from a chalcogenide adsorbent by H+ lifts Cs(I) uptake,” was recently published in the Journal of Hazardous Materials.
Transformative approach: With the KCaSnS, the typically problematic H+ ions in acidic wastewater enhance the Cs+ adsorption process. Essentially, the Ca2+ ions from KCaSnS are leached out by H+ and Cs+, making way for Cs+.
“Through a transformative approach, the troublesome proton was converted into a functional agent by incorporating Ca2+ into the Sn–S matrix, resulting in a metastable structure,” said Cho. “Moreover, Ca2+ is a harder Lewis acid than Cs+ and can thus leave the lattice easily because of its weaker affinity to the Lewis soft base S2- under acidic conditions. This provides a large enough space for Cs+ to reside after its release from the lattice structure.”
Increased capacity: In the study, the team used the hydrothermal process to synthesize the novel KCaSnS ion-exchange material, which was then used to investigate the adsorption of a nonradioactive isotope of Cs+ in different solutions with pH values ranging from 1 to 13.
The team found that at neutral pH 5.5, the Cs+ adsorption capacity was 370 mg/g, whereas at acidic pH 2, the capacity increased by 68 percent to 620 mg/g. This trend was completely opposite to what previous studies had established.
The researchers attributed this observation to the fact that under neutral conditions, the Ca2+ was leached out only from the interlayers, which accounted for around 20 percent of the total spots available for Cs+ to be adsorbed by the S2- ions in the Sn–S matrix.
In contrast, under highly acidic conditions, nearly 100 percent of Ca2+ ions were leached out from both the interlayer and the backbone structure, allowing more Cs+ ions inside the lattice. Additionally, in all cases, interlayer K+ was involved in the ion exchange.