Nanocarbon coating on the basis of partially reduced graphene oxide

There has been developed an approach to the production of graphene as a result of the thermal reduction of graphene oxide (GO). GO has been synthesized by the use of the modified Hummers method with utilization of sodium nitrate and concentrated sulfuric acid. A paper-like material of 40 - 60 μm in...

Full description

Saved in:
Bibliographic Details
Published inJournal of physics. Conference series Vol. 891; no. 1; pp. 12315 - 12318
Main Authors Bocharov, G S, Budaev, V P, Eletskii, A V, Fedorovich, S D
Format Journal Article
LanguageEnglish
Published Bristol IOP Publishing 10.11.2017
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:There has been developed an approach to the production of graphene as a result of the thermal reduction of graphene oxide (GO). GO has been synthesized by the use of the modified Hummers method with utilization of sodium nitrate and concentrated sulfuric acid. A paper-like material of 40 - 60 μm in thickness and 1.2 g/cm3 in density was formed on a filter after deposition from dispersion. The material was cut onto samples of about 15×25 mm2 in size which were experienced to the thermal treatment at various temperatures between 100 and 800 °C. This resulted in a set of GO samples reduced to various degrees. The degree of reduction was determined on the basis of measurements of the conductivity. Along with that the evolution of samples density was studied as the annealing temperature was enhanced. The analysis of the X-ray photoelectron spectra of partially reduced GO permitted the determination of the dynamics of changing the chemical composition of the material in the process of the thermal treatment. The analysis of Raman spectra of the GO samples indicates rather high degree of the disordering of the material. A possibility of the usage of the material produced as a nanocarbon coating in experiments on the interaction of high intense liquid flows with a wall surface is discussed.
ISSN:1742-6588
1742-6596
DOI:10.1088/1742-6596/891/1/012315