Zeolite/CuFe2O4 nanocomposites
(NCs) were
synthesized using the coprecipitation technique with different concentrations
of CuFe2O4 nanoparticles (NPs) to optimize the
capacity of zeolite to cation exchange and study its antibacterial
activities. UV–vis, Fourier-transform infrared (FTIR), X-ray
diffraction (XRD), field emission scanning electron microscopy (FESEM),
energy-dispersive X-ray (EDX), Brunauer–Emmett–Teller
(BET), and thermogravimetric analysis were utilized to characterize
the NCs. XRD patterns revealed a slight shift in the peaks while the
amount of CuFe2O4 increased. The CuFe2O4 NPs were distributed uniformly throughout the zeolite
framework, and the basic structure of the zeolite was intact, as shown
by FESEM and EDX. The addition of 6 wt % CuFe2O4 NPs to the zeolite framework reduced the BET-specific surface area
from 336 to 187 m2/g. The thermal stability of the samples
increased as the amount of CuFe2O4 NPs increased.
Magnetic saturation of NCs was in the range of 10–41 emu/g,
indicating suitability for manipulation under an external magnetic
field. NCs (6 wt %) demonstrated significant antibacterial activity
against different species of bacteria. The efficacy of the antibacterial
agent enhanced with increasing the CuFe2O4 NPs,
reaching 98% against Escherichia coli. Antibacterial activity was also studied throughout the sequential
magnetic separation and recycling phases, and nanocomposite had a
strong antibacterial activity after 7 cycles of recycling, making
them potentially valuable tools in drug delivery systems, wound healing
and tissue engineering, and other biomedical applications.