Lanthanides
are a group of important elements and have
been widely
used in many fields. Their separation is crucial for technical applications,
but it remains a troublesome task due to their subtly different properties.
Herein, novel nanoporous sulfonic covalent organic frameworks were
synthesized by the Schiff base reaction of 1,3,5-tris(p-formylphenyl)benzene (TFPB) and 2,5-diaminobenzene-1,4-disulfonic
acid (DABDA) under mild conditions, which were defined as TFPB-DABDA
iCOFs and used for highly selective adsorption separation of lanthanide
elements. These iCOFs have uniform morphology, good stability, and
excellent adsorption separation ability. The experiment results indicate
that the adsorption capacity of TFPB-DABDA iCOFs is highly sensitive
to the ionic radius. It means that the larger the size difference
between ions, the higher the separation selectivity, especially in
the early lanthanides (La3+, Ce3+, Pr3+, Nd3+, Sm3+, Eu3+, and Gd3+) and late lanthanides (Tb3+, Dy3+, Ho3+, Er3+, Tm3+, and Lu3+).
The separation mechanism of lanthanide elements by TFPB-DABDA iCOFs
may be related to the sulfonic acid groups in the ordered channels
of the COFs. This work develops a simple and efficient strategy for
the synthesis of iCOFs, which shows a promising application of effective
adsorption separation of lanthanides.