Selective strontium adsorption using synthesized sodium titanate in aqueous solution.

Amorphous sodium titanates were synthesized using a mid-temperature sol-gel method for evaluation as selective adsorbents of strontium in the presence of cesium or metal cations (Al3+, Mg2+, Ca2+, and Mn2+) from aqueous solution. Synthesized sodium titanate showed high adsorption capacity and selectivity for strontium. The maximum adsorption capacity of strontium by sodium titanate was 193.93 mg g-1 in aqueous solution containing an initial concentration of 5 mM (438.60 mg L-1) strontium and 5 mM (666.67 mg L-1) cesium, and this sodium titanate removed 99.9% of the strontium and 40.67% of cesium from an aqueous solution that had an initial concentration of 1.14 mM (100 mg L-1) strontium and 0.75 mM (100 mg L-1) cesium. Strontium adsorption by synthesized sodium titanate followed pseudo-second-order kinetics and a generalized Langmuir isotherm model, and reached an adsorption equilibrium within 1 h with high adsorption capacity at equilibrium. Adsorbed strontium onto synthesized sodium titanate showed the behavior of forming a strontium titanate structure with a titanate frame via surface precipitation.

Low-Temperature Continuous Flow Synthesis of Metal Ammonium Phosphates.

The synthesis of the high performance inorganic materials essential to the quality of modern day life is hindered by traditionalist attitudes and reliance on outdated methods such as batch syntheses. While continuous flow methods have been extensively adopted in pharmaceutical circles, they remain largely unexplored for the preparation of inorganic compounds, despite higher efficiency, safety and versatility. In this publication, we demonstrate a step-change for the synthesis of metal ammonium phosphates through conversion of the extant batch process to a low-temperature continuous regime, exhibiting a tenfold increase in throughput combined with a significant decrease in particle size.