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Comparison of the activities of C2N and BCNO towards Congo red degradation
- Source :
- Zaguán. Repositorio Digital de la Universidad de Zaragoza, instname
- Publication Year :
- 2019
-
Abstract
- An n-type organic carbon nitride semiconductor, C2N, was synthesized by the pyrolysis of uric acid, and its properties were investigated by scanning electron and transmission electron microscopies, X-ray powder diffraction, and vibrational, UV-visible and X-ray photoelectron spectroscopies. This novel material, composed of crystalline flakes, featured a broad absorption centered at 700 nm, possibly due to charge transfer, and a 2.49 eV band gap. Its catalytic performance was assessed for the treatment of effluents with the diazo dye Congo red, comparing it with that of boron carbon nitrogen oxide, BCNO. Both wide band gap semiconductors exhibited decolorizing activity in the dark, although the mechanisms were different and were not photocatalytic: BCNO was more effective towards the adsorption-coordination due to the presence of B-O, while C2N was effective towards the adsorption and the advancement of the oxidation reaction. Their kinetic constants (0.19 and 0.02 min−1 for BCNO and C2N, respectively) were comparable to those of intermetallic compounds studied for azo dyes degradation in dark conditions. In view of the high color removal efficiency (97% after 20 min) and good reusability of BCNO, this study suggests a potential application of this catalyst for wastewater treatment, alone or in combination with C2N.
- Subjects :
- Materials science
Band gap
Oxide
chemistry.chemical_element
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
Condensed Matter Physics
01 natural sciences
0104 chemical sciences
Catalysis
Congo red
chemistry.chemical_compound
Adsorption
Chemical engineering
chemistry
Photocatalysis
General Materials Science
0210 nano-technology
Boron
Pyrolysis
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Zaguán. Repositorio Digital de la Universidad de Zaragoza, instname
- Accession number :
- edsair.doi.dedup.....0a0a3a63a1b66d104f60df7435cf376c