Login / Signup

Poly(sodium acrylate)-Modified Magnetite Nanoparticles for Separation of Heavy Metals from Aqueous Solutions.

Magdalena BobikIrena KorusKarol SynoradzkiJacek WojnarowiczDorota BiniaśWłodzimierz Biniaś
Published in: Materials (Basel, Switzerland) (2022)
Two types of magnetite nanoparticles: unmodified (Fe 3 O 4 NPs), and modified with poly(sodium acrylate) (Fe 3 O 4 /PSA NPs) were synthesized by the co-precipitation method and characterized using different techniques: X-ray diffraction (XRD), transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), Brunauer-Emmett-Teller (BET) adsorption, Fourier-transform infrared spectroscopy (FTIR). Additionally, magnetic properties and the effect of pH on the zeta potential were analyzed for both types of nanoparticles. Magnetites were used as adsorbents for seven heavy metal ions (Zn(II), Cu(II), Ni(II), Cd(II), Pb(II), Cr(III), Cr(VI)) within the pH range of 3-7. Research revealed nanometric particle sizes, a specific surface area of 140-145 m 2 /g, and superparamagnetic properties of both tested materials. Moreover, the presence of PSA functional groups in modified magnetite was confirmed, which lowered the pH of the isoelectric point. Both types of magnetite were effective metal ion adsorbents, with metal cations more effectively removed on Fe 3 O 4 /PSA NPs and Cr(VI) anions on Fe 3 O 4 NPs. The adsorption of most of the examined cations (performed at pH = 5) can be well described by the Langmuir isotherm model, whereas the adsorption of Cr(VI) ions on modified magnetite correlated better with the Freundlich model. The Dubinin-Radushkevich model confirmed that chemisorption is the predominant process. The adsorption of all metal ions was well-characterized by the pseudo-second-order kinetic model.
Keyphrases
  • aqueous solution
  • heavy metals
  • prostate cancer
  • electron microscopy
  • risk assessment
  • ionic liquid
  • radical prostatectomy
  • oxide nanoparticles
  • high resolution
  • magnetic resonance imaging
  • single cell
  • mass spectrometry