Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/163
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSamanta, S.
dc.contributor.authorSrivastava, R.
dc.date.accessioned2016-08-03T05:46:53Z
dc.date.available2016-08-03T05:46:53Z
dc.date.issued2016-08-03
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/163
dc.description.abstractNanocrystalline CuCo2O4 was synthesized in the presence of ammonium fluoride and urea. Material was characterized by the complementary combination of X-ray diffraction, N2-adsorption, ultraviolet-visible diffuse reflectance spectroscopy, field enhanced scanning electron microscopic and transmission electron microscopic techniques. Electrochemical sensor based on CuCo2O4 was developed for the detection of organic water pollutants hydrazine and metol. For the comparative purpose, CuO and Co3O4 were synthesized and electrochemical sensors based on these materials were evaluated under the identical condition. CuCo2O4 exhibited excellent electro catalytic activity, stability, sensitivity, and selectivity in the detection of these organic pollutants. Under the optimum condition, a wide linear range was obtained from 32 nM–5000 μM and 20 nM–1000 μM with a limit of detection of 8 nM and 6 nM for hydrazine and metol, respectively at economical CuCo2O4 modified electrode. The analytical performance of the developed sensor was demonstrated in the determination of hydrazine and metol in different real samples such as river water, tap water and metol in photographic solution with satisfactory results.en_US
dc.language.isoen_USen_US
dc.subjectMetal oxideen_US
dc.subjectSpinelsen_US
dc.subjectElectrocatalytic oxidationen_US
dc.subjectHydrazineen_US
dc.subjectMetolen_US
dc.titleCuCo2O4 based economical electrochemical sensor for the nanomolar detection of hydrazine and metolen_US
dc.typeArticleen_US
Appears in Collections:Year-2016

Files in This Item:
File Description SizeFormat 
1-s2.0-S1572665716303708-main.pdf2.58 MBAdobe PDFView/Open    Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.