ABSTRACT
The alkaline activation of a carbonized graphene oxide/dextrin mixture yielded a carbon-based nanoscale material (AC-TR) with a unique highly porous structure. The BET-estimated specific surface area of the material is 3167 m2/g, which is higher than the specific surface area of a graphene layer. The material has a density of 0.34 g/cm3 and electrical resistivity of 0.25 Ω·cm and its properties were studied using the elemental analysis, transmission electron microscopy (TEM), electron diffraction (ED), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray induced Auger electron spectroscopy (XAES), and electron energy loss spectroscopy (EELS) in the plasmon excitation range. From these data, we derive an integral understanding of the structure of this material. The concentration of sp3 carbon atoms was found to be relatively low with an absolute value that depends on the measurement method. It was shown that there is no graphite-like (002) peak in the electron and X-ray diffraction pattern. The characteristic size of a sp2-domain in the basal plane estimated from the Raman spectra was 7 nm. It was also found that plasmon peaks in the EELS spectrum of AC-TR are downshifted compared to those of graphite.
ABSTRACT
A novel mesoporous carbon nanostructured material was prepared and characterized by scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, thermogravimetry, and X-ray diffractometry. The material demonstrated high-speed and high-adsorption capacities of 827.5 and 2484.5 mg g-1 for methyl orange (MO) and malachite green (MG) dyes in 10 min. The kinetic data were fitted to pseudo-first- and pseudo-second-order, external and intraparticle diffusion, and Elovich models, whereas the isotherm data were adjusted to the Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, and Langmuir-Freundlich isotherms (Sips). It was found that MO and MG adsorption was limited by chemical interactions and mixed diffusion. Besides, the physical process was elucidated through free energy values (E = 2.56 and 0.049 kJ mol-1 for the MO and MG, respectively). Methyl orange adsorption mostly occurred through ion exchange and electrostatic interactions, and at lower MO concentrations, through chemical interactions and surface complexation as well. Malachite green adsorption took place only on lower-energy sites. Thus, it can be concluded that the adsorbent proposed herein possessed high-speed and high-adsorption capacity. Therefore, it can be considered as promising in removing the reported dye pollutants.
