Abstract

A novel cetyltrimethylammonium bromide (CTABr) modified purified-bentonite (p-Bent)-MOF composite (CTABr/p-Bent-Co2(OH)2BDC) was first prepared to study the uranium(VI) adsorption from a variety of carbonate solutions. The experiments showed that at pH 8.0, the high concentration of carbonates and halides significantly suppressed the UVI adsorption. Compared with Co2(OH)2BDC (4.3 ± 0.9 mg·g−1), p-Bent (47.2 ± 3.7 mg·g−1), and CTABr/p-Bent (104.8 ± 0.8 mg·g−1), this ternary composite achieved an improved adsorption capacity of 111.7 ± 1.4 mg·g−1. The XPS spectra and DFT calculations indicated that carbonates and halides can compete for free uranyl ions with the –COOH and –OH groups on the composite surface. Particularly, CO32− and F− can inhibit the UVI adsorption from carbonate solutions by forming uranyl carbonates and uranyl fluorides. The Br− anion exchange and electrostatic attraction were demonstrated to be the dominant mechanisms for UVI adsorption on the composite, together with the –COOH/–OH complexation. This work presents a feasible strategy to prepare new clay-based multicomponent composites for extracting uranium from carbonate solutions, and provides new insight into the understanding of uranium adsorption in natural waters.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call