Simultaneous removal of Co(II) and 1-naphthol by core–shell structured Fe3O4@cyclodextrin magnetic nanoparticles
•Core–shell structured Fe3O4@CD MNPs are prepared via chemical co-precipitation approach.•Fe3O4@CD MNPs are low-cost and eco-friendly as the raw materials are abundant and harmless.•Fe3O4@CD MNPs can be easily separated from the aqueous phase with a magnet.•Fe3O4@CD MNPs exhibit favorable performanc...
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Published in | Carbohydrate polymers Vol. 114; pp. 521 - 529 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
19.12.2014
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •Core–shell structured Fe3O4@CD MNPs are prepared via chemical co-precipitation approach.•Fe3O4@CD MNPs are low-cost and eco-friendly as the raw materials are abundant and harmless.•Fe3O4@CD MNPs can be easily separated from the aqueous phase with a magnet.•Fe3O4@CD MNPs exhibit favorable performance toward the removal of Co(II) and 1-naphthol.•Fe3O4@CD MNPs show great application potential in environmental protection field.
Herein, β-cyclodextrin (β-CD) was introduced on the surfaces of Fe3O4 particles via the chemical co-precipitation approach. The as-prepared Fe3O4@CD MNPs can be easily separated from the aqueous phase with a magnet. The removal performance of Fe3O4@CD MNPs toward Co(II) and 1-naphthol were investigated by using the batch technique. The maximum sorption capacities of Fe3O4@CD MNPs toward Co(II) and 1-naphthol are higher than a series of adsorbent materials. The simultaneous removal of Co(II) and 1-naphthol is achieved via the binding of Co(II) on the external surface sites of Fe3O4@CD MNPs and the incorporation of 1-naphthol into the hydrophobic cavity of surface-coated β-CD. The Fe3O4@CD MNPs exhibit favorable removal performance toward Co(II) and 1-naphthol from the simulated effluent. The experimental results herein suggest that Fe3O4@CD MNPs can be used as cost-effective material for the purification of co-contaminated water systems. |
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ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2014.08.072 |