It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Graphitic carbon nitride (g–C3N4), an organic photocatalyst was reported to have beneficial properties to be used in wastewater treatment applications. However, g–C3N4, in its bulk form was found to have poor photocatalytic degradation efficiency due to its inherent limitations such as poor specific surface area and fast electron–hole pair recombination rate. In this study, we have tuned the physiochemical properties of bulk g–C3N4 by direct thermal exfoliation (TE–g–C3N4) and examined their photocatalytic degradation efficiency against abundant textile dyes such as methylene blue (MB), methyl orange (MO), and rhodamine B (RhB). The degradation efficiencies for MB, MO, and RhB dyes are 92 ± 0.18%, 93 ± 0.31%, and 95 ± 0.4% respectively in 60 min of UV light irradiation. The degradation efficiency increased with an increase in the exfoliation temperature. The prepared catalysts were characterized using FTIR, XRD, FE-SEM, EDAX, BET, and UV-DRS. In BET analysis, TE–g–C3N4 samples showed improved surface area (48.20 m2/g) when compared to the bulk g–C3N4 (5.03 m2/g). Further, the TE–g–C3N4 had 2.98 times higher adsorption efficiency than the bulk ones. The free radicals scavenging studies revealed that the superoxide radicals played an important role in the photodegradation for dyes, when compared to the hydroxyl radical (.OH) and the photo-induced holes (h+), Photoluminescence (PL) emission and electrochemical impedance spectroscopy (EIS) spectra of TE–g–C3N4 indicated a lowered electron–hole pairs’ recombination rate and an increased photo-induced charge transfer respectively. Further, the TE–g–C3N4 were found to have excellent stability for up to 5 cycles with only a minor decrease in the activity from 92% to 86.2%. These findings proved that TE–g–C3N4 was an excellent photocatalyst for the removal and degradation of textile dyes from wastewater.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Vellore Institute of Technology, Department of Chemistry, School of Advanced Sciences, Vellore, India (GRID:grid.412813.d) (ISNI:0000 0001 0687 4946); Vellore Institute of Technology, Human Organ Manufacturing Engineering (HOME), Lab, Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), Vellore, India (GRID:grid.412813.d) (ISNI:0000 0001 0687 4946)
2 National Taipei University of Technology, Department of Electro-Optical Engineering, Taipei, Taiwan (GRID:grid.412087.8) (ISNI:0000 0001 0001 3889)
3 Vellore Institute of Technology, Department of Chemistry, School of Advanced Sciences, Vellore, India (GRID:grid.412813.d) (ISNI:0000 0001 0687 4946)
4 Vellore Institute of Technology, Human Organ Manufacturing Engineering (HOME), Lab, Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), Vellore, India (GRID:grid.412813.d) (ISNI:0000 0001 0687 4946)