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Comparative Study of Catalytic Activity of Recyclable Au/Fe 3 O 4 Microparticles for Reduction Of 2,4-Dinitrophenol and Anionic, Cationic Azo Dyes
We synthesized Au/Fe O microparticles. Initially, citrate-capped Fe O micro-sized particles were synthesized by the co-precipitation method with an excess amount of trisodium citrate. Gold ions were reduced on the surface of citrate-capped Fe O and grew as gold sub-microparticles with an average dia...
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Published in: | ChemistryOpen (Weinheim) 2024-09, Vol.13 (9), p.e202300297 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We synthesized Au/Fe
O
microparticles. Initially, citrate-capped Fe
O
micro-sized particles were synthesized by the co-precipitation method with an excess amount of trisodium citrate. Gold ions were reduced on the surface of citrate-capped Fe
O
and grew as gold sub-microparticles with an average diameter of 210 nm on the surface. The characteristic SPR peak of gold nanoparticles on the surface of Fe
O
was detected at 584 nm, whereas the absorption in the near-infrared region was increased. SEM images has proved that the synthesized Au/Fe
O
composite microparticles has an average diameter of 1.7 micrometers. The results of XRD patterns proved the existence of both crystal phases of Fe
O
and Au particles. To investigate the catalytic activity, the reaction rate constant of reduction of 2,4-dinitrophenol (2,4-DNP) and degradation of Congo red (CR), and methylene blue (MB) with NaBH4 in the presence of Au/Fe
O
catalyst was monitored by UV-Vis spectroscopy. The initial reaction rate constant calculated from the change in characteristic peak absorptions of 2,4-dinitrophenol was 3.97×10
s
, while the reaction rate constants for the degradation of CR and MB were 9.72×10
s
and 14.25×10
s
respectively. After 5 cycles, Au/Fe
O
microparticles preserved 99 % of the reaction rate constant, exhibiting considerable recycling efficiency in the reduction of nitro groups. |
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ISSN: | 2191-1363 2191-1363 |
DOI: | 10.1002/open.202300297 |