Macroporous alginate substrate-bound growth of Fe super(0) nanoparticles with high redox activities for nitrate removal from aqueous solutions
The agglomeration of zero-valent iron nanoparticles (Fe super(0) NPs) can significantly decrease the effective surface area of nanoparticles and thus reduce their catalytic performance. To avoid such agglomeration, a two-part Fe super(0) NP-immobilization approach was developed: (1) The fabrication...
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Published in | Chemical engineering journal (Lausanne, Switzerland : 1996) Vol. 298; pp. 206 - 213 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
15.08.2016
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Subjects | |
Online Access | Get full text |
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Summary: | The agglomeration of zero-valent iron nanoparticles (Fe super(0) NPs) can significantly decrease the effective surface area of nanoparticles and thus reduce their catalytic performance. To avoid such agglomeration, a two-part Fe super(0) NP-immobilization approach was developed: (1) The fabrication of a macroporous alginate substrate (MAS) that provided a large surface area capable of sustaining a high load of stable and well-dispersed Fe super(0) NPs (26.06 wt.%). (2) A facile chemical reductive growth procedure to generate Fe super(0) NPs (ca. 50-100 nm) that are covalently anchored to the surface of the MAS. The macroporous alginate substrate-supported Fe super(0) nanoparticles (Fe super(0) NPs/MAS) removed >96.5% of nitrates from an aqueous solution within 30 min, whereas unsupported Fe super(0) NPs removed only 44.7% of nitrates over a longer period of time. These results demonstrate that MAS acts in a way to prevent the agglomeration of Fe super(0) NPs and, in turn, to promote their redox activity compared to unsupported Fe super(0) NPs. On the basis of our experimental results, a grow mechanism of Fe super(0) NPs on the MAS was proposed, and potential implications for environmental applications of Fe super(0) NPs/MAS were discussed. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1385-8947 |
DOI: | 10.1016/j.cej.2016.03.113 |