Evaluation of quinoline photodegradation from g-C3N4/TiO2 heterostructured materials

Autores

  • Jhonatan Douglas Moura de Oliveira UFPE Autor
  • Alan Gomes Camara UFPE Autor
  • Santiago Arias UFPE Autor
  • José Geraldo de Andrade Pacheco UFPE Autor
  • Celmy Maria Bezerra de Menezes Barbosa UFPE Autor

Palavras-chave:

band-gap, contamination, photocatalyst, heterojunction

Resumo

The commercial TiO₂-P25 is widely used in the photocatalytic degradation of recalcitrant organic compounds; however, it has a band-gap energy of 3.2 eV, meaning it is activated to generate unstable radicals only through ultraviolet radiation [1]. C-N based materials have often been used in heterojunctions with TiO₂, as they improve the optical and electronic properties of the photocatalyst [2]. The objective of this study is to evaluate the synthesis of a 10%g-C₃N₄/TiO₂ heterostructured material, obtained from melamine, and to compare it with commercial TiO₂ P25 in the photocatalytic degradation of quinoline. The catalyst was synthesized from 2 g of melamine dissolved in 40 mL of ethanol, followed by homogenization for 15 min. Then, 4.5 g of TiO₂ P25 was added, and the mixture was homogenized for 1 h. The system was heated to 60°C to evaporate the ethanol. Subsequently, thermal treatment was carried out in a muffle furnace at a heating rate of 5°C min-1, reaching 500°C
and maintaining that temperature for 180 min. The photocatalysis tests were conducted in a batch reactor containing 200 mL of quinoline solution, with a concentration of 20 mg L-1 at pH 6.5, and 0.5 g L-1 of catalyst under O₂ bubbling. The system was kept in the dark for 30 min to achieve adsorption equilibrium, followed by 120 min under artificial light simulating sunlight. The polychromatic light source (UV-A and UV-B) used was a 300W OSRAM E27 lamp, with an irradiance of 4.6 mW cm-2. The
material was characterized using XRD, TGA, and N₂ adsorption/desorption techniques. X-ray diffractograms confirmed the presence of TiO₂ in the anatase and rutile phases. TGA analysis revealed that the minimum temperature required for calcination to obtain 10%g-C₃N₄/TiO₂ is 500 °C. Between 550 °C and 700 °C, thermal decomposition of g-C₃N₄ may occur, leading to the formation of graphite and the release of N₂ [3]. The addition of g-C₃N₄ resulted in a slight decrease in the surface area of
commercial TiO₂ P25 (STiO₂ = 52 m2 g-1 to 48 m2 g-1 in 10%g-C₃N₄/TiO₂). Quinoline degradation after 90 min showed an efficiency of 37.2% by photolysis, 94.2% with commercial TiO₂ P25, and 92.4% with the 10%g-C₃N₄/TiO₂ composite, highlighting the high performance of the catalysts compared to simple photolysis. The heterostructured material showed
excellent photocatalytic performance in quinoline degradation.

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Referências

1. Camara, A. G., Sousa, R. P., Costa, M. J., Dantas, E. J., Frety, R., Luz Jr, G. E., Barbosa, Celmy M. B. M., Almeida, L. C. Arias, S., Pacheco, J. G. A. (2024). Heterostructured g-C3N4-TiO2 nanocomposites applied to p-toluic acid

degradation under solar light-induced photocatalytic process. Journal of Photochemistry and Photobiology A: Chemistry, 116021. 2. Abdallah, S. S., Maridevaru, M. C., Al Marzouqi, F., Selvaraj, R. (2024). Green synthesis of TiO2@ g-C3N4 nanocomposites for the photocatalytic degradation of pesticides and toxic organics present in water and wastewater. Journal of Photochemistry and Photobiology A: Chemistry, 116015. 3. Li, X.; J., Shen, L.; Ma, Y.; Lei, W.; Cui, Q.; Zou, G. (2009). Preparation and characterization of graphitic carbon nitride through pyrolysis of melamine. Applied Physics A, 94, 387-392.

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Publicado

15-11-2024

Edição

Seção

Catálise ambiental, fotocatálise e eletrocatálise.

Como Citar

OLIVEIRA, Jhonatan Douglas Moura de; GOMES CAMARA, Alan; ARIAS, Santiago; PACHECO, José Geraldo de Andrade; BARBOSA, Celmy Maria Bezerra de Menezes. Evaluation of quinoline photodegradation from g-C3N4/TiO2 heterostructured materials. XIV Encontro de Catálise do Norte, Nordeste e Centro-Oeste, Brasil, 2024. Disponível em: https://submissao.sbcat.org/index.php/xivencat/article/view/57. Acesso em: 27 dez. 2024.

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