4.7 Article

Adsorption mechanism of methylene blue on oxygen-containing functional groups modified graphitic carbon spheres: Experiment and DFT study

Journal

APPLIED SURFACE SCIENCE
Volume 540, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2020.148386

Keywords

Ammonium persulfate; Graphitic carbon spheres; Sodium dodecyl sulfate; Methylene blue adsorption; DFT calculation

Funding

  1. National Natural Science Foundation of China [51872210, 51672194]
  2. Program for Innovative Teams of Outstanding Young and Middle-aged Researchers in the Higher Education Institutions of Hubei Province [T201602]
  3. Key Program of Natural Science Foundation of Hubei Province, China [2017CFA004]

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Graphitic carbon spheres were prepared using glucose as the starting material and modified to increase the number of functional groups on the surface, leading to improved adsorption performance mainly influenced by charge transfer.
Graphitic carbon spheres (GCSs) were prepared using glucose as the starting material. The adsorption performance of as-prepared GCSs, ammonium persulfate (AP-GCSs) and sodium dodecyl sulfate (SDS-GCSs) modified graphitic carbon spheres were investigated. More -COOH, -C-OH and -S-O functional groups attached on the surface of the modified GCSs compared to original counterparts, and the adsorption capacities of AP-GCSs and SDS-GCSs were 295.5 mg/g and 681.4 mg/g, respectively, which was about 1.6 and 3.7 times of that original GCSs. During the adsorption process, the adsorption sites of methylene blue (MB) (the S, N1 and N2 atoms) formed chemical bonds with S and O atoms in the oxygen-containing functional groups (-COOH, -C-OH, -COOH/C-OH and -SO4). Density functional theory (DFT) calculations revealed that the adsorption energy between MB adsorption sites (S, N1, N2) and -SO4 decreased from about -4.30 to -6.38 eV for S, -3.90 to -4.67 eV for N1 and -4.74 to -6.30 eV for N2, demonstrating stronger electronic charge transferring compared with that of -COOH and -C-OH. This could be the driving force for the improved adsorption performance of the modified samples.

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