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Ion exchange properties of a cesium ion selective titanosilicate

Journal Article · · Solvent Extraction and Ion Exchange
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  1. Texas A&M Univ., College Station, TX (United States)
The ion exchange properties of crystalline and amorphous phases of a sodium titanosilicate towards alkali and alkaline earth cations has been examined. Potentiometric titration of the crystalline phase in the proton form, H{sub 2}Ti{sub 2}O{sub 3}(SiO{sub 4}), showed that 80% of the sodium ion sites could be occupied to pH=12 and only 25% of the exchange sites could be filled by Cs{sup +}. However, when an equal concentration of Na{sup +} was present in the Cs{sup +} solution, the cesium loading was reduced to 5.6% (0.47meq/g) of the theoretical IEC. This loading is further reduced to less than 0.1 meq/g in solutions approximating the sodium content of nuclear waste solutions, i.e., 5-6 M NaNO{sub 3}, 1-3 M NaOH. This low capacity limits the usefulness of this exchanger to waste solutions less than 10{sup -5}-10{sup -6} M in Cs{sup +}. The amorphous phase exhibits a very high affinity for Sr{sup 2+} but also for Ba{sup 2+} and Ca{sup 2+} in alkaline solution. These ions could serve as interferences for selective Sr{sup 2+} removal from nuclear waste solutions. Sodium titanium silicate has a tunnel structure. The low capacity of the exchanger for Cs{sup +} stems form the fact that only a few of the exchange sites can be filled with Cs{sup +} in the presence of Na{sup +} and still maintain charge balance. 12 refs., 7 figs., 2 tabs.
Sponsoring Organization:
USDOE
OSTI ID:
232474
Journal Information:
Solvent Extraction and Ion Exchange, Journal Name: Solvent Extraction and Ion Exchange Journal Issue: 2 Vol. 14; ISSN 0736-6299; ISSN SEIEDB
Country of Publication:
United States
Language:
English