Molten Salt Synthesis of Carbon Nitride Nanostructures at Different Temperatures for Extracting Uranium from Seawater

Abstract

The importance of extracting uranium from seawater with a green, efficient, and economical strategy has long been paid attention but still faces challenges of low uranyl concentration, high salinity, and competition with carbonate ions. Herein, we report a tunable carbon nitride nanostructure synthesized using molten salt, whose adsorption capacity and photocatalytic activity can be adjusted with the synthesis temperature. With increased synthesis temperature, the adsorption capacity and photocatalytic activity both showed a trend of an increase first and then a decrease. The carbon nitride nanostructure obtained at 550 °C (CN 550 ) exhibited the highest photocatalysis-assisted extraction ability (9.4 times higher than that of g-C 3 N 4 ) and that obtained at 600 °C (CN 600 ) showed the highest adsorption capacity of 1387.0 mg/g, which is 51 times higher than that of g-C 3 N 4 . In addition to the outstanding adsorption ability, CN 600 has a verified extraction rate of nearly 100% of uranyl carbonate with a pH of 6.0, 7.1, and 8.0 in simulated seawater.

Thermal reflux to synthesise C3N4 nanostructures with high yield and enhanced photocatalytic activity in hydrogen evolution

“…It also has the advantage of high stability, simple preparation, and being nonhazardous to the environment. 2,3 So many methods have been explored to synthesize g-C 3 N 4 , such as thermal pyrolysis, 4,5 a supramolecular pre-assembly strategy, 6,7 a microwave-assisted heating strategy, 8 a template-assisted strategy, [9][10][11] a molten salt strategy, [12][13][14][15] a co-catalyst loading, 16 and so on.…”