Crystallization of Sodium Titanium Silicate with Sitinakite Topology:  Evolution from the Sodium Nonatitanate Phase

• Published in: Chemistry of materials 2004-09, Vol.16 (19), p.3659-3666
• Main Authors: Medvedev, Dmitri G, Tripathi, Akhilesh, Clearfield, Abraham, Celestian, Aaron J, Parise, John B, Hanson, Jonathan
• Format: Article
• Language: English
• Subjects: Applied sciences; Chemistry; Condensed matter: electronic structure, electrical, magnetic, and optical properties; Condensed matter: structure, mechanical and thermal properties; CRYSTALLIZATION; Exact sciences and technology; General and physical chemistry; MATERIALS SCIENCE; NATIONAL SYNCHROTRON LIGHT SOURCE; PHASE STUDIES; Physicochemistry of polymers; Physics; SODIUM SILICATES; TITANIUM SILICATES
• ISSN: 0897-4756; 1520-5002
• DOI: 10.1021/cm049479a

Titanium silicate (TS) with sitinakite topology and composition Na2Ti2O3SiO4·2H2O has received considerable attention because of its high ion-exchange selectivity toward cesium and strontium. In this paper we report the results of the studies of the crystallization process of TS with a combination of ex and in situ experiments. The effects of various parameters, such as gel composition, time, and temperature of the synthesis, on crystallinity and composition of the final product have been investigated. In situ X-ray powder diffraction studies carried out during the synthesis of TS revealed that the process begins with the formation of layered sodium nonatitanate (SNT) with chemical composition Na4Ti9O20·xH2O, which is also an excellent ion exchanger, selective for strontium and actinides. The pathway of transformation of SNT to the final product is sensitive to alkalinity of the starting gels. At high hydroxide concentration the reaction resulted in the formation of sodium titanium oxide silicate, Na2TiSiO5, which has the mineral natisite topology. This study has revealed a pathway for the synthesis of a combined SNT−TS exchanger for removal of Cs, Sr, and actinides by a single-step in-tank process.