Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources

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  • Central Metallurgical Research and Development Institute, Cairo
  • Kuwait Institute for Scientific Research
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OriginalspracheEnglisch
Aufsatznummer102797
FachzeitschriftJournal of Environmental Chemical Engineering
Jahrgang7
Ausgabenummer1
Frühes Online-Datum19 Nov. 2018
PublikationsstatusVeröffentlicht - Feb. 2019

Abstract

The non-doped and non-metal tri-doped TiO 2 were prepared and used as photocatalysts activated by low-cost and low powered irradiation sources (LED) for the degradation of 4-aminoantipyrine (4-AAP) for the first time. The nano-spindle-like brookite phase with high-quality was hydrothermally synthesized at 200 °C for 20 h, in the absence of glycine. The nano-spherical-like anatase mixed with nano-rod-like brookite TiO 2 were synthesized using different molarities of glycine. The N-C-S tridoped B/A TiO 2 was synthesized by mixing optimum non-doped TiO 2 with thiourea followed by calcination at 450 °C. The findings exhibited that the absorption edges of the obtained TiO 2 shifted from UV to visible region as a result of non-metal tri-doping. The N-C-S tri-doped/TiO 2 was confirmed by XPS analysis. The effect of pH values, the catalyst loadings and 4-AAP concertation were performed for degradation of 4-AAP employing solar and LED irradiation sources (UV-A and visible light). The complete degradation of 4-AAP (pH 3, 0.02 g L -1 ) under solar, UV-A LED, and visible light sources was achieved using N-C-S-tri-doped B/A TiO 2 photocatalyst (0.4 g L -1 ). PL spectra confirmed that tri-doped TiO 2 hetrojunction reduce the e-/h + recombination.

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Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources. / Khedr, Tamer M.; El-Sheikh, Said M.; Ismail, Adel A. et al.
in: Journal of Environmental Chemical Engineering, Jahrgang 7, Nr. 1, 102797, 02.2019.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Khedr, TM, El-Sheikh, SM, Ismail, AA & Bahnemann, D 2019, 'Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources', Journal of Environmental Chemical Engineering, Jg. 7, Nr. 1, 102797. https://doi.org/10.1016/j.jece.2018.11.042
Khedr, T. M., El-Sheikh, S. M., Ismail, A. A., & Bahnemann, D. (2019). Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources. Journal of Environmental Chemical Engineering, 7(1), Artikel 102797. https://doi.org/10.1016/j.jece.2018.11.042
Khedr TM, El-Sheikh SM, Ismail AA, Bahnemann D. Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources. Journal of Environmental Chemical Engineering. 2019 Feb;7(1):102797. Epub 2018 Nov 19. doi: 10.1016/j.jece.2018.11.042
Khedr, Tamer M. ; El-Sheikh, Said M. ; Ismail, Adel A. et al. / Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources. in: Journal of Environmental Chemical Engineering. 2019 ; Jahrgang 7, Nr. 1.
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abstract = "The non-doped and non-metal tri-doped TiO 2 were prepared and used as photocatalysts activated by low-cost and low powered irradiation sources (LED) for the degradation of 4-aminoantipyrine (4-AAP) for the first time. The nano-spindle-like brookite phase with high-quality was hydrothermally synthesized at 200 °C for 20 h, in the absence of glycine. The nano-spherical-like anatase mixed with nano-rod-like brookite TiO 2 were synthesized using different molarities of glycine. The N-C-S tridoped B/A TiO 2 was synthesized by mixing optimum non-doped TiO 2 with thiourea followed by calcination at 450 °C. The findings exhibited that the absorption edges of the obtained TiO 2 shifted from UV to visible region as a result of non-metal tri-doping. The N-C-S tri-doped/TiO 2 was confirmed by XPS analysis. The effect of pH values, the catalyst loadings and 4-AAP concertation were performed for degradation of 4-AAP employing solar and LED irradiation sources (UV-A and visible light). The complete degradation of 4-AAP (pH 3, 0.02 g L -1 ) under solar, UV-A LED, and visible light sources was achieved using N-C-S-tri-doped B/A TiO 2 photocatalyst (0.4 g L -1 ). PL spectra confirmed that tri-doped TiO 2 hetrojunction reduce the e-/h + recombination. ",
keywords = "4-Aminoantipyrine, Brookite/anatase, Non-metal doped TiO, Photodegradation, Solar-visible light",
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T1 - Photodegradation of 4-aminoantipyrine over nano-titania heterojunctions using solar and LED irradiation sources

AU - Khedr, Tamer M.

AU - El-Sheikh, Said M.

AU - Ismail, Adel A.

AU - Bahnemann, Detlef

N1 - Funding Information: This work was supported by Science and Technological Development Fund (STDF) , Academy of Scientific Research & Technology, Cairo, Egypt , under Grant No. ID 25503.

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Y1 - 2019/2

N2 - The non-doped and non-metal tri-doped TiO 2 were prepared and used as photocatalysts activated by low-cost and low powered irradiation sources (LED) for the degradation of 4-aminoantipyrine (4-AAP) for the first time. The nano-spindle-like brookite phase with high-quality was hydrothermally synthesized at 200 °C for 20 h, in the absence of glycine. The nano-spherical-like anatase mixed with nano-rod-like brookite TiO 2 were synthesized using different molarities of glycine. The N-C-S tridoped B/A TiO 2 was synthesized by mixing optimum non-doped TiO 2 with thiourea followed by calcination at 450 °C. The findings exhibited that the absorption edges of the obtained TiO 2 shifted from UV to visible region as a result of non-metal tri-doping. The N-C-S tri-doped/TiO 2 was confirmed by XPS analysis. The effect of pH values, the catalyst loadings and 4-AAP concertation were performed for degradation of 4-AAP employing solar and LED irradiation sources (UV-A and visible light). The complete degradation of 4-AAP (pH 3, 0.02 g L -1 ) under solar, UV-A LED, and visible light sources was achieved using N-C-S-tri-doped B/A TiO 2 photocatalyst (0.4 g L -1 ). PL spectra confirmed that tri-doped TiO 2 hetrojunction reduce the e-/h + recombination.

AB - The non-doped and non-metal tri-doped TiO 2 were prepared and used as photocatalysts activated by low-cost and low powered irradiation sources (LED) for the degradation of 4-aminoantipyrine (4-AAP) for the first time. The nano-spindle-like brookite phase with high-quality was hydrothermally synthesized at 200 °C for 20 h, in the absence of glycine. The nano-spherical-like anatase mixed with nano-rod-like brookite TiO 2 were synthesized using different molarities of glycine. The N-C-S tridoped B/A TiO 2 was synthesized by mixing optimum non-doped TiO 2 with thiourea followed by calcination at 450 °C. The findings exhibited that the absorption edges of the obtained TiO 2 shifted from UV to visible region as a result of non-metal tri-doping. The N-C-S tri-doped/TiO 2 was confirmed by XPS analysis. The effect of pH values, the catalyst loadings and 4-AAP concertation were performed for degradation of 4-AAP employing solar and LED irradiation sources (UV-A and visible light). The complete degradation of 4-AAP (pH 3, 0.02 g L -1 ) under solar, UV-A LED, and visible light sources was achieved using N-C-S-tri-doped B/A TiO 2 photocatalyst (0.4 g L -1 ). PL spectra confirmed that tri-doped TiO 2 hetrojunction reduce the e-/h + recombination.

KW - 4-Aminoantipyrine

KW - Brookite/anatase

KW - Non-metal doped TiO

KW - Photodegradation

KW - Solar-visible light

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JO - Journal of Environmental Chemical Engineering

JF - Journal of Environmental Chemical Engineering

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ER -

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