Please use this identifier to cite or link to this item:
https://idr.l2.nitk.ac.in/jspui/handle/123456789/12814
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Prasad, R. | |
dc.contributor.author | Lolakshi, M.K. | |
dc.contributor.author | Bhat, B.R. | |
dc.date.accessioned | 2020-03-31T08:42:11Z | - |
dc.date.available | 2020-03-31T08:42:11Z | - |
dc.date.issued | 2016 | |
dc.identifier.citation | Synthetic Metals, 2016, Vol.219, , pp.26-32 | en_US |
dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/12814 | - |
dc.description.abstract | The Cobalt-Nickel-reduced graphene oxide ternary composite was prepared using eco-friendly, solvent-free and low temperature CVD method where in metal formates were used as metal precursor. The structure, composition and morphology of synthesized samples were characterized by several related techniques like X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The catalytic efficiency towards reduction of an organic pollutant such as 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) was explored and the reaction parameters like temperature, weight ratio of the composite was optimised and rate constant of the reactions were measured. The results show 8% Co-Ni-rGO are having high catalytic efficiency and can complete the reduction reaction within 250 s at 45 C. Furthermore, catalyst being magnetically separable shows high stability after ten successive reactions. Hence, the Co-Ni-rGO composite can be a potential promising material to catalyse the reduction of 4-NP. 2016 Elsevier B.V. All rights reserved. | en_US |
dc.title | RGO supported Co-Ni bimetallic magnetically separable nanocatalysts for the reduction of 4-Nitrophenol | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.