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Synthesis Dynamics of Graphite Oxide

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F18%3APU128976" target="_blank" >RIV/00216305:26620/18:PU128976 - isvavai.cz</a>

  • Result on the web

    <a href="https://www-sciencedirect-com.ezproxy.lib.vutbr.cz/science/article/pii/S0040603118300960" target="_blank" >https://www-sciencedirect-com.ezproxy.lib.vutbr.cz/science/article/pii/S0040603118300960</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.tca.2018.03.017" target="_blank" >10.1016/j.tca.2018.03.017</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis Dynamics of Graphite Oxide

  • Original language description

    Graphite oxide synthesis dynamics were investigated using a sampling technique. The synthesis of graphite oxide was carried out by a modified Hummers’ method. Small samples of the solid phase (30–50 mg) were collected from the reaction mixture and analyzed by thermogravimetric analysis, differential scanning calorimetry, scanning electron microscopy, X-ray diffraction, Raman spectroscopy, energy dissipative X-ray spectroscopy, and X-ray photoelectron spectroscopy. The strongest oxidation was detected 10 min after the start of the synthesis, i.e., after the addition of KMnO4, when the formation of the graphite oxide phase with intercalated guest molecules begins. The intercalation of graphite started after 30 min of synthesis when the temperature was increased to 35°C. The addition of ice into the reaction mixture leads to the increase in the COOH group concentration, whereas the concentration of C=O groups slightly changes, and the concentration of the C–O and C=O groups remains almost constant. It was found that the degree of oxidation of graphite oxide exhibited complex change, and H2O2 plays a significant role not only in the removal of impurities but also in the increase in the GO oxidation degree that is reflected by a higher concentration of oxygen-containing functional groups. Differential scanning calorimetry and thermogravimetric analysis data confirmed that the additions of ice and H2O2 induce the stronger formation of surface functional groups instead of intercalated guest species.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Thermochimica Acta

  • ISSN

    0040-6031

  • e-ISSN

    1872-762X

  • Volume of the periodical

    663

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    11

  • Pages from-to

    165-175

  • UT code for WoS article

    000436912000021

  • EID of the result in the Scopus database

    2-s2.0-85045031576