A thiacalixarene-functionalized
graphene oxide (GO-TC4A) composite
was synthesized via esterification and polymerization of thiacalix[4]arene
(TC4A) onto the graphene oxide (GO) surface and used to adsorb radionuclides
from aqueous solution. The GO-TC4A composite showed high adsorption
capacities (337.84, 101.11, and 164.47 mg·g–1 for Nd(III), Sr(II), and Rb(I) ions, respectively) and excellent
efficiency in removing a high density of radionuclides from water,
compared to GO. The adsorption capacity of GO-TC4A was found to rise
with increasing solution pH, reaching a maximum at pH values of 6–7,
7–9, and 4–5 for Nd(III), Sr(II), and Rb(I) ions, respectively.
The correlation coefficients (R
2 >
0.999)
implied that the pseudo-second-order model was most suitable to represent
the adsorption kinetics. Four adsorption isotherm models were discussed
comparatively, and the fitting results indicate that the Freundlich
model was the most suitable method to describe the adsorption process
of Nd(III) ions, whereas the Langmuir model best described that of
Sr(II) and Rb(I) ions. FTIR and XPS analysis showed that the adsorption
of radionuclides on the GO-TC4A composite is mostly controlled by
chemisorption for strong chelation. Thermodynamic studies implied
that the adsorption toward Nd(III), Sr(II), and Rb(I) ions was an
endothermic and spontaneous natural process.