Issue 20, 2024

Surface engineering: binary Mg,Fe-LDH·xFe3O4 nanocomposites for improved magnetic solid-phase extraction of pharmaceuticals from aqueous solution

Abstract

In this work, binary Mg,Fe-LDH·xFe3O4 (x = 0 to 2.0) nanocomposites were prepared via the in situ growth of Mg,Fe-layered double hydroxides (LDHs) onto magnetite nanoparticles and applied for the removal of diclofenac motives. These materials were prepared by a simple prolonged sonication method and systematically characterized by several techniques (e.g. XRD, VRM, SEM, FTIR, TEM, etc.). The XRD patterns of the magnetic nanocomposites confirm the formation of both LDHs and magnetic phases. The intricate surface functional groups of the starting components played pivotal roles in the formation of magnetic composites, according to FTIR spectra. The hexagonal plate-like morphology of the Mg,Fe-LDHs and Mg,Fe-LDH·xFe3O4 samples is evident from TEM data. The Mg,Fe-LDH·1.0Fe3O4 nanocomposite exhibited high agglomeration of the magnetite nanoparticles, which broke their layered structure. Various influencing factors (e.g., concentration, pH medium, and contact time) that are known to influence the adsorption properties of materials were systematically studied to clarify the mechanism of the adsorption process. To assess the safety of the adsorbents, the effect of the adsorbed DCF on the release of metal ions from the LDHs structure was also monitored. Moreover, the Mg,Fe-LDH·xFe3O4 (x = 0.1 to 1.0) nanocomposites can be quickly separated from the 400 mL solution by an external NdFeB magnet before and after the magnetic solid-phase extraction process. The capacity of the magnetic nanocomposites to adsorb diclofenac increased with increasing solution pH. At 25 °C and pH = 7.5, the maximum adsorption capacities for Mg,Fe-LDH·0.1Fe3O4 and Mg,Fe-LDH·0.3Fe3O4 were 153.2 mg g−1 (0.48 mmol g−1) and 143.2 mg g−1 (0.45 mmol g−1), respectively, which do not exceed the capacities for the starting Mg,Fe-LDHs (158.1 mg g−1). Further results indicated that the adsorption isotherm for diclofenac anion retention could be fitted to the Langmuir equation. The FTIR and XRD data indicate that organic molecules are adsorbed on the obtained materials by electrostatic and complex-forming processes without significant anion-exchange reactions. Moreover, after 3 regeneration cycles, the magnetic nanocomposites still retained a highly ordered structure and morphology with a magnetic response.

Graphical abstract: Surface engineering: binary Mg,Fe-LDH·xFe3O4 nanocomposites for improved magnetic solid-phase extraction of pharmaceuticals from aqueous solution

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
11 Jun 2024
Accepted
10 Sep 2024
First published
12 Sep 2024
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2024,5, 8145-8163

Surface engineering: binary Mg,Fe-LDH·xFe3O4 nanocomposites for improved magnetic solid-phase extraction of pharmaceuticals from aqueous solution

T. Hubetska, V. Demchenko and N. Kobylinska, Mater. Adv., 2024, 5, 8145 DOI: 10.1039/D4MA00609G

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements