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Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light

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dc.contributor.author Sambaza, S
dc.contributor.author Maity, Arjun
dc.contributor.author Pillay, K
dc.date.accessioned 2019-04-10T10:59:45Z
dc.date.available 2019-04-10T10:59:45Z
dc.date.issued 2019-02
dc.identifier.citation Sambaza, S., Maity, A. & Pillay, K. 2019. Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light. Journal of Environmental Chemical Engineering, vol 7(1), pp. 1-12 en_US
dc.identifier.issn 2213-3437
dc.identifier.issn 2213-2929
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S221334371930003X
dc.identifier.uri https://doi.org/10.1016/j.jece.2019.102880
dc.identifier.uri http://hdl.handle.net/10204/10943
dc.description Copyright: 2019 Elsevier. Due to copyright restrictions, the attached PDF file only contains the abstract version of the full-text item. For access to the full-text item, please consult the publisher's website. The definitive version of the work is published in Journal of Environmental Chemical Engineering, vol 7(1), pp. 1-12 en_US
dc.description.abstract PANI supported Ag@TiO(sub)2 nanocomposite was synthesized via oxidative polymerization of aniline on Ag@TiO(sub)2. The Ag@TiO(sub)2 nanocomposite was synthesized by the photo reduction of Ag nanoparticles on hydrothermally synthesized TiO(sub)2 nanofibers. Raman analysis revealed that the anatase phase of TiO2 was synthesized showing typical peaks at 195 cm(sup)-1, 396 cm(sup)-1, 514 cm(sup)-1, and 637 cm(sup)-1. The incorporation of PANI, a carbonaceous material was confirmed by appearance of D-band and G-band in Ag@TiO(sub)2-PANI that were located at 1505 cm-1 and 1603 cm-1 respectively. X-ray diffraction (XRD) analysis confirmed the anatase phase of TiO(sub)2 was synthesized. Transmission electron microscopy analysis (TEM) analysis revealed that TiO(sub)2 nanofibers were synthesized successfully and Ag nanoparticles of different sizes were deposited on their surface. X-ray Photon Spectroscopy (XPS) survey scan of the Ag@TiO(sub)2-PANI-nanocomposite revealed that the nanocomposite was made from C, O, Ag, Ti, and N. DRS and Tauc`s plot estimated the band gap of Ag@TiO2-PANI to be 3.0 eV A comparative study of the photocatalytic performance of Ag@TiO2-PANI catalyst showed better degradation performance under both conditions than pristine TiO(sub)2, and Ag@TiO(sub)2 with a degradation of up to 99.7% under visible light irradiation. The degradation experiments showed that the reactive species that were dominant in the degradation of BPA were h(sup)+ and %O(sup)2-. Ag@TiO(sub)2-PANI nanocomposite was re-used to degrade BPA for up to four cycles without losing much of its photocatalytic ability with a removal of at least 90% in the fourth cycle. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartofseries Workflow;22241
dc.subject Bisphenol A en_US
dc.subject UV en_US
dc.subject Visible light en_US
dc.subject Ag@TiO2-PANI en_US
dc.subject X-ray photoelectron spectroscopy en_US
dc.title Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light en_US
dc.type Article en_US
dc.identifier.apacitation Sambaza, S., Maity, A., & Pillay, K. (2019). Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light. http://hdl.handle.net/10204/10943 en_ZA
dc.identifier.chicagocitation Sambaza, S, Arjun Maity, and K Pillay "Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light." (2019) http://hdl.handle.net/10204/10943 en_ZA
dc.identifier.vancouvercitation Sambaza S, Maity A, Pillay K. Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light. 2019; http://hdl.handle.net/10204/10943. en_ZA
dc.identifier.ris TY - Article AU - Sambaza, S AU - Maity, Arjun AU - Pillay, K AB - PANI supported Ag@TiO(sub)2 nanocomposite was synthesized via oxidative polymerization of aniline on Ag@TiO(sub)2. The Ag@TiO(sub)2 nanocomposite was synthesized by the photo reduction of Ag nanoparticles on hydrothermally synthesized TiO(sub)2 nanofibers. Raman analysis revealed that the anatase phase of TiO2 was synthesized showing typical peaks at 195 cm(sup)-1, 396 cm(sup)-1, 514 cm(sup)-1, and 637 cm(sup)-1. The incorporation of PANI, a carbonaceous material was confirmed by appearance of D-band and G-band in Ag@TiO(sub)2-PANI that were located at 1505 cm-1 and 1603 cm-1 respectively. X-ray diffraction (XRD) analysis confirmed the anatase phase of TiO(sub)2 was synthesized. Transmission electron microscopy analysis (TEM) analysis revealed that TiO(sub)2 nanofibers were synthesized successfully and Ag nanoparticles of different sizes were deposited on their surface. X-ray Photon Spectroscopy (XPS) survey scan of the Ag@TiO(sub)2-PANI-nanocomposite revealed that the nanocomposite was made from C, O, Ag, Ti, and N. DRS and Tauc`s plot estimated the band gap of Ag@TiO2-PANI to be 3.0 eV A comparative study of the photocatalytic performance of Ag@TiO2-PANI catalyst showed better degradation performance under both conditions than pristine TiO(sub)2, and Ag@TiO(sub)2 with a degradation of up to 99.7% under visible light irradiation. The degradation experiments showed that the reactive species that were dominant in the degradation of BPA were h(sup)+ and %O(sup)2-. Ag@TiO(sub)2-PANI nanocomposite was re-used to degrade BPA for up to four cycles without losing much of its photocatalytic ability with a removal of at least 90% in the fourth cycle. DA - 2019-02 DB - ResearchSpace DP - CSIR KW - Bisphenol A KW - UV KW - Visible light KW - Ag@TiO2-PANI KW - X-ray photoelectron spectroscopy LK - https://researchspace.csir.co.za PY - 2019 SM - 2213-3437 SM - 2213-2929 T1 - Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light TI - Enhanced degradation of BPA in water by PANI supported Ag/TiO2 nanocomposite under UV and visible light UR - http://hdl.handle.net/10204/10943 ER - en_ZA


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