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Chemically stable ionic viologen-organic network: an efficient scavenger of toxic oxo-anions from water

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dc.contributor.author SAMANTA, PARTHA en_US
dc.contributor.author CHANDRA, PRIYANSHU en_US
dc.contributor.author DUTTA, SUBHAJIT en_US
dc.contributor.author DESAI, AAMOD V. en_US
dc.contributor.author GHOSH, SUJIT K. en_US
dc.date.accessioned 2019-02-18T04:04:03Z
dc.date.available 2019-02-18T04:04:03Z
dc.date.issued 2018-08 en_US
dc.identifier.citation Chemical Science, 9(40), 7874-7881. en_US
dc.identifier.issn 2041-6520 en_US
dc.identifier.issn 2041-6539 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1881
dc.identifier.uri https://doi.org/10.1039/C8SC02456A en_US
dc.description.abstract Detoxification of water has been demonstrated with a viologen-based cationic organic network (compound-1), which was stable not only in water, but also in acidic and basic media. The presence of free exchangeable Cl− ions inside the network of compound-1 and a high physiochemical stability of the materials offered a suitable scope for the capture of hazardous anionic pollutants from water. Rapid removal of the toxic water pollutant and carcinogenic chromate (CrO42−) from water was shown with compound-1. Furthermore, the oxo-anion of the radioactive isotope of technetium (99Tc), i.e. the TcO4− ion, also counts as a toxic water pollutant and by using surrogate anions (MnO4− and ReO4−), a model capture study was performed. Notably, compound-1 showed high capacity values for each of the oxo-anions and these were comparable to some of the well-performing compounds reported in the literature. Furthermore, to check the real time aspect, removal of all of the aforementioned anions from water was demonstrated, even in the presence of other concurrent anions. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.subject 2018 en_US
dc.title Chemically stable ionic viologen-organic network: an efficient scavenger of toxic oxo-anions from water en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Science en_US
dc.publication.originofpublisher Foreign en_US


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