Molecules (Oct 2022)

A Novel Nanocomposite Based on Triazine Based Covalent Organic Polymer Blended with Porous g-C<sub>3</sub>N<sub>4</sub> for Photo Catalytic Dye Degradation of Rose Bengal and Fast Green

  • Nachimuthu Venkatesh,
  • Govindhasamy Murugadoss,
  • Abdul Azeez Ashif Mohamed,
  • Manavalan Rajesh Kumar,
  • Shaik Gouse Peera,
  • Pachagounder Sakthivel

DOI
https://doi.org/10.3390/molecules27217168
Journal volume & issue
Vol. 27, no. 21
p. 7168

Abstract

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Metal free visible light active photocatalysts of covalent organic polymers (COPs) and polymeric graphitic carbon nitride (g-C3N4) are interesting porous catalysts that have enormous potential for application in organic pollutant degradation. Imine condensation for COPs, and thermal condensation for g-C3N4 were used to produce the catalysts. FT-IR, Raman, NMR, UV-Vis Spectroscopy, X-ray diffraction, and scanning electron microscopy studies were used to investigate the structural, optical, and morphological features of the metal free catalysts. We have constructed COPs with a π-electron deficient (Lewis acidic) triazine core and π -electron rich (Lewis basic) naphthalene and anthraquinone rings coupled by -O and -N donors in this study. Furthermore, the prepared Bulk-g-C3N4 (B-GCN) was converted to porous g-C3N4 (P-GCN) using a chemical oxidation process, and the generated P-GCN was efficiently mixed with the COP to create a novel nanocomposite for photocatalytic application. Using the anthraquinone-based COP and P-GCN (1:1 ratio, PA-GCN) catalyst, the highest photodegradation efficiencies for the polymeric graphitic carbon nitride of 88.2% and 82.3% were achieved using the Fast green (FG) and Rose bengal (RB) dyes, respectively. The rate constant values of 0.032 and 0.024/min were determined for FG and RB degradation, respectively. Higher activity may be related to the incorporation of COP and PA-GCN, which act significantly well in higher visible light absorption, have superior reactive oxygen generation (ROS), and demonstrate an excellent pollutant–catalyst interaction.

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