The
selective capture of radioactive cesium, strontium, and lanthanides
from liquid nuclear waste is of great significance to environmental
remediation and human health. Herein, the rapid and selective removal
of Cs+, Sr2+, and Eu3+ ions is achieved
by two metal sulfides (FJSM-SnS-2 and FJSM-SnS-3). Both structures
feature [Sn3S7]
n
2n– layers with the mixed cations
of [CH3NH3]+ and [Bmmim]+ (1-butyl-2,3-dimethylimidazolium) as templates. However, the ratios
and arrangements of mixed cations in the interlayered spaces are distinct.
It is unprecedented that [CH3NH3]+ and [Bmmim]+ in FJSM-SnS-2 are alternatingly arranged
in different interlayered spaces, whereas they in FJSM-SnS-3 are located
in the same interlayered spaces. It is the first time that the ionic
liquid cation and protonated organic amine have been simultaneously
incorporated into metal sulfides. Both compounds show high capacities,
rapid kinetics, and a wide pH active range for Cs+, Sr2+, and Eu3+. Even under excess Na+ ions,
both show excellent selectivity in capturing trace Sr2+ and Eu3+ ions. FJSM-SnS-3 presents the highest K
d
Eu to date. They still retain high
removal efficiency even after intense β and γ radiation.
Moreover, it is first confirmed by the in situ tracking method of
mass spectrometry that the large-sized [Bmmim]+ ions are
exchangeable. It is found that the arrangement of cations between
interlayered spaces is a crucial factor affecting ion exchange performance.
This work will likely change the consensus that large-sized organic
cations are difficult to be exchanged and thus further highlight the
great potential of metal sulfide ion exchangers for radionuclide remediation.