The
introduction of a functional moiety into a covalent organic
framework (COF) is of great significance in promoting its wide applications.
Here we show the one-pot synthesis of carboxyl-functionalized COF-TzDBd
via the direct condensation of 1,3,5-tris(4-formyl-phenyl) triazine
(Tz) and 4,4′-diamino-[1,1′-biphenyl]-2,2′-dicarboxylic
acid (DBd). The prepared TzDBd showed good crystallinity, mesoporous
pores, and high chemical stability. It was applied for ultrafast adsorption
and the efficient elimination of triphenylmethane dyes. The adsorption
isotherms, adsorption thermodynamics, kinetics, and reusability of
the prepared carboxyl-COF were investigated in detail. The adsorption
of crystal violet (CV) and brilliant green (BG) on TzDBd followed
the pseudo-second-order adsorption kinetic model and reached equilibrium
within 2 min at the initial concentration of 100 mg L–1. The adsorption of triphenylmethane dyes on TzDBd fit well with
the Langmuir adsorption model and gave the maximum adsorption capacities
of 307.7 and 276.1 mg g–1 for CV and BG, respectively.
The predesigned mesoporous pores, conjugated phenyl structure, and
negatively charged carboxyl groups on TzDBd significantly facilitate
the adsorption kinetics for large cationic triphenylmethane dyes.
The ultrafast kinetics, high adsorption capacity, and good reusability
endow the carboxyl-functionalized COF with great potential for removing
triphenylmethane dyes from an aqueous environment.