Polypyrrole modified Fe0-loaded graphene oxide for the enrichment of uranium(vi) from simulated seawaterElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt02819b
Extraction of uranium( vi ) from seawater has attracted much attention for its potential use in the nuclear energy field. In this work, we synthesized graphene oxide-polypyrrole (GO-PPy) through pyrrole monomer polymerization on graphene oxide (GO) with an aqueous solution at low temperature and pre...
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Main Authors | , , , , , , , , |
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Format | Journal Article |
Published |
25.09.2018
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Online Access | Get full text |
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Summary: | Extraction of uranium(
vi
) from seawater has attracted much attention for its potential use in the nuclear energy field. In this work, we synthesized graphene oxide-polypyrrole (GO-PPy) through pyrrole monomer polymerization on graphene oxide (GO) with an aqueous solution at low temperature and prepared reduced graphene oxide-polypyrrole-zero-valent iron (rGO-PPy-Fe
0
) composites by chemical deposition. We characterized rGO-PPy-Fe
0
using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The rGO-PPy-Fe
0
composites were investigated for the removal of uranium from aqueous solution and simulated seawater. The experimental results demonstrated that the rGO-PPy-Fe
0
adsorbent possessed a superior capacity for the adsorption of uranium at mg g
−1
and μg g
−1
at the pH value of seawater. The adsorption process conformed to the pseudo-second-order rate equation and the Langmuir isotherm model. Based on X-ray photoelectron spectroscopy (XPS), we revealed the possible adsorption mechanism of uranium onto rGO-PPy-Fe
0
, which simulated a prospective potential of the adsorbent in seawater.
A high selectivity uranium (
vi
) adsorbent was synthesized and used for removal of uranium (
vi
). The idiographic adsorption capacity is attributed to coordination and chemical reduction of uranium (
vi
) ions with rGO-PPy-Fe
0
. |
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Bibliography: | 10.1039/c8dt02819b Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c8dt02819b |