Experimental study demonstrates highly selective mercury ion capture by flexible covalent triazine polyamides in aqueous media, indicating high adsorption capacity and environmental stability.
There are a number of sulfur-containing adsorbents that can trap Hg 2+ in aqueous solutions with high selectivity. However, these adsorbents often require a large number of sulfur atoms in their structure. Additionally, the five- and six-membered ring structures are among the most stable. It would therefore be great to incorporate the stable five- and six-membered ring structures into covalent organic polymers (COPs), thus reducing the number of sulfur atoms required. In this study, we introduced a flexible structure to enhance the neighboring active sites more effectively. We termed the prepared adsorbent materials as sulfur-modified flexible covalent triazine polyamides (SF-CTPas). The adsorption of Hg 2+ in water by SF-CTPa is a chemisorption process, with a maximum adsorption capacity of 1970 mg/g. Our experiments, characterizing the acid and alkali resistance, thermogravimetry, and cycle regeneration, show that SF-CTPa is a highly stable adsorption material. Meanwhile, the primary chelation mechanism of SF-CTPa for Hg 2+ entails the stable six- and five-membered ring structures capturing the Hg 2+ by means of flexible amides and adjacent nitrogen or sulfur atoms. Additionally, we placed the SF-CTPa with adsorbed Hg 2+ in an aqueous solution for 7 days and found no Hg 2+ in the solution.
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Xiong et al. (2025) studied this question.
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