# Facile synthesis of Fe3O4@pyrogallol-formaldehyde resin@Ag core–shell nanomaterials for the catalytic degradation of contaminants

**Authors:** Liping Jiang, Yang Xi, Ziyi Xu, Zewen Song, Yuwei Cui, Haijun Zhou

PMC · DOI: 10.1039/d5ra02755a · RSC Advances · 2025-07-08

## TL;DR

This paper introduces a new core-shell nanomaterial that effectively degrades pollutants by controlling the charge interactions between the catalyst and contaminants.

## Contribution

A novel Fe3O4@PGFR@Ag core-shell nanomaterial is developed to prevent noble metal nanoparticle aggregation and enhance catalytic performance.

## Key findings

- Negatively charged Fe3O4@PGFR@Ag showed 90% higher catalytic activity for RhB compared to the CTAB-modified version.
- Positively charged Fe3O4@PGFR@Ag-CTAB exhibited 124% higher catalytic activity for MO compared to the unmodified version.
- Charge matching between catalyst and pollutants significantly impacts catalytic performance.

## Abstract

Noble metal nanoparticles (NPs) show excellent performance in catalysis, but their strong aggregation effect can lead to a decrease in or even disappearance of their catalytic activity. In this study, Fe3O4@pyrogallol-formaldehyde resin@Ag (Fe3O4@PGFR@Ag) nanomaterials were synthesized using Fe3O4 as a magnetic core and pyrogallol-formaldehyde resin (PGFR) as a shell layer. The presence of Fe3O4 ensured rapid material recovery. At the same time, the phenolic hydroxyl group in PGFR enabled the in situ reduction of Ag+ to form embedded Ag NPs, effectively avoiding the aggregation and shedding of Ag NPs. Cetyltrimethylammonium bromide (CTAB) was used to modify the surface charge of the catalyst. Results showed that negatively charged Fe3O4@PGFR@Ag exhibited high catalytic activity, with a 90% higher catalytic rate constant for cationic dye rhodamine B (RhB) compared with Fe3O4@PGFR@Ag-CTAB. Positively charged Fe3O4@PGFR@Ag-CTAB showed high catalytic activity, with a 124% higher catalytic rate constant for the anionic dye methyl orange (MO) compared with Fe3O4@PGFR@Ag. Therefore, the matching of the charges of the catalyst and contaminants, which facilitates the adsorption of the pollutants around the catalyst, has a significant impact on the catalytic performance and should be considered in the process of pollutant treatment.

In this study, Fe3O4@PGFR@Ag was synthesized using Fe3O4 as a magnetic core and pyrogallol-formaldehyde resin (PGFR) as a shell layer. Fe3O4@PGFR@Ag exhibited high catalytic activity for RhB. Fe3O4@PGFR@Ag-CTAB showed high catalytic activity for MO.

## Linked entities

- **Chemicals:** Ag (PubChem CID 23954), cetyltrimethylammonium bromide (PubChem CID 5974), rhodamine B (PubChem CID 6694), methyl orange (PubChem CID 23673835)

## Full-text entities

- **Chemicals:** O (MESH:D010100), metal (MESH:D008670), PGFR (-), MO (MESH:C100258), Fe (MESH:D007501), RhB (MESH:C029773), Ag (MESH:D012834), -CTAB (MESH:D000077286)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12236299/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12236299/full.md

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Source: https://tomesphere.com/paper/PMC12236299