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Recognizing adsorption of aqueous Cr(VI), As(III), Cd(II), and Pb(II) ions by amino groups hollow polymer adsorbent
The mechanism from the molecular level and the selectivity for the removal of metal ions from aqueous has become a hotspot in current water treatment. In this study, a sulphydryl-modified hollow polymer adsorbent was designed with intrinsic amine and grafted sulphydryl groups for efficient uptake of...
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Published in: | Journal of environmental chemical engineering 2024-02, Vol.12 (1), p.111701, Article 111701 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The mechanism from the molecular level and the selectivity for the removal of metal ions from aqueous has become a hotspot in current water treatment. In this study, a sulphydryl-modified hollow polymer adsorbent was designed with intrinsic amine and grafted sulphydryl groups for efficient uptake of Cr(VI), As(III), Cd(II), and Pb(II) by taking advantage of their properties of abundant functional groups, discrete hollow chambers, and high porosity. Interestingly, the benzenoid amine/quinoid imine functional groups have a stronger affinity for Cr(VI) than Cd(II) or As(III) and Pb(II). The formation of approximately 65.7% Cr(III) indicates the redox reaction from Cr(VI) to Cr(III). The electron-donating comes from benzenoid amine and oxidized to quinoid imine or protonated oxidized nitrogen units (-N = +) with Cr(VI) reduced to Cr(III) for the increase of more than double of quinoid imine and a new functional group of -N = +. Ion exchange between –COO- groups and As(III)/Cd(II), the chelation of –SH groups for Pb(II)/As(III) are plausible mechanisms.
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•A sulphydryl-modified hollow polymer adsorbent was designed.•The mechanism of Cr(VI) reduction was explained from the molecular level.•A high adsorption capacity of 343 mg g−1 for Cr(VI) has been achieved. |
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ISSN: | 2213-3437 2213-3437 |
DOI: | 10.1016/j.jece.2023.111701 |