Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation
C and N codoped TiO2 nanoparticles were synthesized via a solvothermal method. The degradation of Rhodamine B by the photocatalyst C, N-TiO2 was investigated under visible-light irradiation generated by using a 36 W compact fluorescent lamp which is characterized by wavelengths from 400 to 650 nm. T...
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2020-01-01
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Online Access: | http://dx.doi.org/10.1155/2020/4310513 |
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author | Thuy Thi Thanh Le Trinh Dinh Tran |
author_facet | Thuy Thi Thanh Le Trinh Dinh Tran |
author_sort | Thuy Thi Thanh Le |
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description | C and N codoped TiO2 nanoparticles were synthesized via a solvothermal method. The degradation of Rhodamine B by the photocatalyst C, N-TiO2 was investigated under visible-light irradiation generated by using a 36 W compact fluorescent lamp which is characterized by wavelengths from 400 to 650 nm. The structure and properties of the obtained photocatalyst have been systematically investigated using X-ray diffraction, TEM, UV-Vis, FT-IR, and BET techniques. The experimental results revealed that C, N codoped TiO2 nanoparticles were successfully synthesized, with an average diameter of 9.1 nm. C, N-TiO2 nanoparticles exhibited an energy band gap of 2.90 eV, which were lower than pristine TiO2 (3.34 eV), C-TiO2 (3.2 eV), and N-TiO2 (3.03 eV). The degradation of Rhodamine B by C, N-TiO2 indicated that, under visible-light irradiation, the optimal dose of the photocatalyst was 1.8 g/L, and the removal of Rhodamine B was almost complete after 3 hours of reaction. The photocatalytic degradation of Rhodamine B in the range of 5–100 mg/L showed that the process followed the first-order kinetics according to the Langmuir–Hinshelwood model. The highest apparent rate constant (0.0427 min−1) was obtained when the initial concentration of Rhodamine B was 5 mg/L, whereas the former decreased with the increase in the initial concentration of Rhodamine B. Moreover, C and N codoped TiO2 nanoparticles presented a high potential for recycling, which was characterized by a removal efficiency of more than 86% after three cycles. |
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spelling | doaj-art-ba0073c6972c4f0fa8a0f47ce9d8ca932025-02-03T01:03:50ZengWileyJournal of Chemistry2090-90632090-90712020-01-01202010.1155/2020/43105134310513Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light IrradiationThuy Thi Thanh Le0Trinh Dinh Tran1Department of Chemistry, Faculty of Science, Qui Nhon University, No. 170 an Duong Vuong Street, Qui Nhon, VietnamVNU Key Laboratory of Advanced Materials for Green Growth, Faculty of Chemistry, University of Science, Vietnam National University, No. 334 Nguyen Trai Street, Hanoi, VietnamC and N codoped TiO2 nanoparticles were synthesized via a solvothermal method. The degradation of Rhodamine B by the photocatalyst C, N-TiO2 was investigated under visible-light irradiation generated by using a 36 W compact fluorescent lamp which is characterized by wavelengths from 400 to 650 nm. The structure and properties of the obtained photocatalyst have been systematically investigated using X-ray diffraction, TEM, UV-Vis, FT-IR, and BET techniques. The experimental results revealed that C, N codoped TiO2 nanoparticles were successfully synthesized, with an average diameter of 9.1 nm. C, N-TiO2 nanoparticles exhibited an energy band gap of 2.90 eV, which were lower than pristine TiO2 (3.34 eV), C-TiO2 (3.2 eV), and N-TiO2 (3.03 eV). The degradation of Rhodamine B by C, N-TiO2 indicated that, under visible-light irradiation, the optimal dose of the photocatalyst was 1.8 g/L, and the removal of Rhodamine B was almost complete after 3 hours of reaction. The photocatalytic degradation of Rhodamine B in the range of 5–100 mg/L showed that the process followed the first-order kinetics according to the Langmuir–Hinshelwood model. The highest apparent rate constant (0.0427 min−1) was obtained when the initial concentration of Rhodamine B was 5 mg/L, whereas the former decreased with the increase in the initial concentration of Rhodamine B. Moreover, C and N codoped TiO2 nanoparticles presented a high potential for recycling, which was characterized by a removal efficiency of more than 86% after three cycles.http://dx.doi.org/10.1155/2020/4310513 |
spellingShingle | Thuy Thi Thanh Le Trinh Dinh Tran Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation Journal of Chemistry |
title | Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation |
title_full | Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation |
title_fullStr | Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation |
title_full_unstemmed | Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation |
title_short | Photocatalytic Degradation of Rhodamine B by C and N Codoped TiO2 Nanoparticles under Visible-Light Irradiation |
title_sort | photocatalytic degradation of rhodamine b by c and n codoped tio2 nanoparticles under visible light irradiation |
url | http://dx.doi.org/10.1155/2020/4310513 |
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