Abstract

Ni0.5Zn0.5Fe2O4 magnetic nanoparticles were synthesized to obtain a new efficient adsorbent for diclofenac sodium (DF) removal. Fourier Transform Infrared (FTIR), Energy Dispersive Spectrometer (EDS), scanning electron microscope (SEM), Brunauer-Emmett-Teller (BET) and vibrating sample magnetometer (VSM) were applied to characterize the prepared adsorbent. These analyses revealed that adsorbent was successfully prepared with averageparticle diameterof about 50 nm and a BET surface area of 168.09 m2/g. The saturation magnetization value of magnetic nanoparticles (MNPs) was found to be 24.90 emu/g, thus, adsorbent was efficiently separated from the solution by a facile and rapid magnetic separation process. The effect of adsorption time, amount of adsorbent, initial pH of the solution, initial diclofenac concentration and temperature on the removal of DF were evaluated. Also, the adsorption data were best fitted to the pseudo-first-order kinetic model and Langmuir isotherm model. The thermodynamics studies suggested spontaneous and exothermic adsorption. The maximum diclofenac adsorption amount of the synthesized nanoadsorbent was 52.91 mg/g, which is higher than many recently studied adsorbents.

Highlights

  • During the last several years, the existence of pharmaceutical compounds in aquatic media has been widely detected

  • Diclofenac adsorption onto Ni0.5Zn0.5Fe2O4 magnetic nanoparticles (MNPs) was investigated in terms of isotherm, kinetic, and thermodynamics

  • The bands at 489 cmÀ1 and 445 cmÀ1 are the characteristic bands of Ni-O and Zn-O, revealing the presence of Ni and Zn in the structure of synthesized Ni0.5Zn0.5Fe2O4 magnetic nanoparticles (Thakur et al ; Sharma et al )

Read more

Summary

Introduction

During the last several years, the existence of pharmaceutical compounds in aquatic media has been widely detected.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.