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Self-assembled kanamycin antibiotic-inorganic microflowers and their application as a photocatalyst for the removal of organic dyes

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dc.contributor.author Jadhav, R.W.
dc.contributor.author La, D.D.
dc.contributor.author More, V.G.
dc.contributor.author Vo, H.T.
dc.contributor.author Nguyen, D.A.
dc.contributor.author Tran, D.L.
dc.contributor.author Bhosale, S.V.
dc.date.accessioned 2020-01-20T06:04:08Z
dc.date.available 2020-01-20T06:04:08Z
dc.date.issued 2020
dc.identifier.citation Scientific Reports. 10; 2020; ArticleID_154. en_US
dc.identifier.uri https://doi.org/10.1038/s41598-019-57044-z
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/5949
dc.description.abstract Construction of hybrid three-dimensional (3D) hierarchical nanostructures via self-assembly of organic and inorganic compounds have recently attracted immense interest from scientists due to their unique properties and promise in a large range of applications. In this article, hybrid flower structures were successfully constructed by self-assembly an antibiotic, kanamycin, with Cu sup(2+). The flower-like morphology was observed by scanning electron microscopy, to be approximately 4 micro m in diameter and about 10 nm in thickness. FTIR spectroscopy and X-ray diffraction confirmed the antibiotic-inorganic hybrid structure was uniform composition, and showed crystallinity due to ordered self-assembly. The hybrid flowers showed high photocatalytic activity towards degradation of methyl blue during 240 minutes under visible light irradiation. A possible mechanism of photocatalytic activity was also proposed, that exposes the inherent advantages in using antibiotic-inorganic hybrid flowers as photocatalysts, where self-assembly can be used to generate active, high surface area structures for photodegradation of pollutants. en_US
dc.publisher Springer en_US
dc.subject Chemistry en_US
dc.title Self-assembled kanamycin antibiotic-inorganic microflowers and their application as a photocatalyst for the removal of organic dyes en_US
dc.type Journal article en_US
dc.identifier.impf y


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