Issue 11, 2019

Protonation of rhodanine polymers for enhancing the capture and recovery of Ag+ from highly acidic wastewater

Abstract

Selective capture and direct recovery of silver ions from highly acidic wastewater are desirable but challenging for sustainable remediation of contamination. In this work, contraposing the characteristics of actual Ag-polluted water, poly-allylrhodanine (PAR) is designed and synthesized as an adsorbent. Different from most reported adsorbents, PAR features a unique acidity-enhanced adsorptivity property, thus achieving an ultrahigh capacity (651.0 mg gāˆ’1) and outstanding selectivity (>100) in the capture of Ag+ from wastewater with strong acidity (pH āˆ’0.2). Moreover, the purity of the reclaimed Ag+ reaches up to 99.80%, delivering an enormous economic benefit. Further characterization and theoretical calculations uncover that the C[double bond, length as m-dash]S and Cā€“S groups on PAR act as adsorption sites to coordinate the Ag+ ions via a special pH-dependent protonation exchange mechanism. In the treatment of actual Ag-polluted water, the treatment capacity of PAR is as high as 4015 bed volumes (BV) per run at pH = āˆ’0.2, which is 100-fold higher than that of commercial resin, highlighting its great potential in practical applications. The wastewater feature-directed design concept and the high-performance adsorbent of PAR reported in this work may be helpful to fill the gap between the experimental laboratory and practical remediation of Ag-containing wastewater.

Graphical abstract: Protonation of rhodanine polymers for enhancing the capture and recovery of Ag+ from highly acidic wastewater

Supplementary files

Article information

Article type
Paper
Submitted
22 Jul 2019
Accepted
07 Sep 2019
First published
12 Sep 2019

Environ. Sci.: Nano, 2019,6, 3307-3315

Protonation of rhodanine polymers for enhancing the capture and recovery of Ag+ from highly acidic wastewater

X. Yin, P. Shao, L. Ding, Y. Xi, K. Zhang, L. Yang, H. Shi and X. Luo, Environ. Sci.: Nano, 2019, 6, 3307 DOI: 10.1039/C9EN00833K

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