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Erschienen in: Journal of Nanoparticle Research 3/2017

01.03.2017 | Research Paper

Generation and thermally adjustable catalysis of silver nanoparticle immobilized temperature-sensitive nanocomposite

verfasst von: Jun Xu, Tao Zhou, Lei Jia, Xiaoke Shen, Xiaohui Li, Huijun Li, Zhouqing Xu, Jianliang Cao

Erschienen in: Journal of Nanoparticle Research | Ausgabe 3/2017

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Abstract

The rise in environmental issues due to the catalytic degradation of pollutants in water has received much attention. In this report, a facile method was developed for the generation of a novel thermosensitive Ag-decorated catalyst, SiO2@PNIPAM@Ag (the average particle size is around 540 nm), through atom transfer radical polymerization (ATRP) and mild reducing reactions. First, poly(N-isopropylacrylamide) (PNIPAM) was used to create a shell around mercapto-silica spheres that allowed for enhanced catalyst support dispersion into water. Second, through a mild reducing reaction, these Ag nanoparticles (NPs) were then anchored to the surface of SiO2@PNIPAM spheres. The resulting catalyst revealed catalytic activity to degrade various nitrobenzenes and organic dyes in an aqueous solution with sodium borohydride (NaBH4) at ambient temperature. The catalytic activity can be adjusted in different temperatures through the aggregation or dispersion of Ag catalyst on the polymer supporters, which is due to the thermosensitive PNIPAM shell. The ease of preparation and efficient catalytic activity of the catalyst can make it a promising candidate for the use in degrading organic pollutants for environmental remediation.

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Metadaten
Titel
Generation and thermally adjustable catalysis of silver nanoparticle immobilized temperature-sensitive nanocomposite
verfasst von
Jun Xu
Tao Zhou
Lei Jia
Xiaoke Shen
Xiaohui Li
Huijun Li
Zhouqing Xu
Jianliang Cao
Publikationsdatum
01.03.2017
Verlag
Springer Netherlands
Erschienen in
Journal of Nanoparticle Research / Ausgabe 3/2017
Print ISSN: 1388-0764
Elektronische ISSN: 1572-896X
DOI
https://doi.org/10.1007/s11051-017-3769-y

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