Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania

This paper reports the photocatalytic degradation of pre-treated palm oil mill effluent (POME) over a Pt-doped titania photocatalyst. Pt loading on the titania was varied from 0.25 to 1.0 wt% via alcohol reduction of chloroplatinic acid (H2PtCl6). XRD characterization of the photocatalysts showed th...

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Main Authors: Cheng, C. K., Mohd Rizauddin, Deraman, Khan, Maksudur R.
Format: Article
Language:English
English
Published: Elsevier Ltd 2015
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Online Access:http://umpir.ump.edu.my/id/eprint/7467/1/Evaluation_of_the_photocatalytic_degradation_of_pre-treated_palm_oil_mill_effluent_%28POME%29_over_Pt-loaded_titania.pdf
http://umpir.ump.edu.my/id/eprint/7467/4/Evaluation%20of%20the%20Photocatalytic%20Degradation%20of%20Pre-Treated%20Palm%20Oil%20Mill%20Effluent%20%28Pome%29%20Over%20Pt-Loaded%20Titania.pdf
http://umpir.ump.edu.my/id/eprint/7467/
http://dx.doi.org/10.1016/j.jece.2014.10.016
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spelling my.ump.umpir.74672018-08-24T07:43:51Z http://umpir.ump.edu.my/id/eprint/7467/ Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania Cheng, C. K. Mohd Rizauddin, Deraman Khan, Maksudur R. TP Chemical technology This paper reports the photocatalytic degradation of pre-treated palm oil mill effluent (POME) over a Pt-doped titania photocatalyst. Pt loading on the titania was varied from 0.25 to 1.0 wt% via alcohol reduction of chloroplatinic acid (H2PtCl6). XRD characterization of the photocatalysts showed that the photo-active anatase phase was still intact after the photocatalyst synthesis while the XPS spectrum confirmed that the deposited Pt was free from the Cl and existed as Pt0 and Pt4+. In addition, the UV–vis diffuse reflectance measurement indicated an improved light energy absorption in the visible light spectrum. Moreover, the band gap energy (3.16–3.17 eV) was reduced when titania was doped with Pt, compared to the pristine titania with 3.20 eV. The 0.5 wt% Pt/TiO2 photocatalyst offered the most effective degradation of pre-treated POME under the irradiation of 100 W of UV light (10%) and also visible light (11%), respectively, over a loading of 0.2 g/L. Significantly, the maximum 0.5 wt% Pt/TiO2 photocatalyst loading determined from the current work was 1.0 g/L. Elsevier Ltd 2015 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/7467/1/Evaluation_of_the_photocatalytic_degradation_of_pre-treated_palm_oil_mill_effluent_%28POME%29_over_Pt-loaded_titania.pdf application/pdf en http://umpir.ump.edu.my/id/eprint/7467/4/Evaluation%20of%20the%20Photocatalytic%20Degradation%20of%20Pre-Treated%20Palm%20Oil%20Mill%20Effluent%20%28Pome%29%20Over%20Pt-Loaded%20Titania.pdf Cheng, C. K. and Mohd Rizauddin, Deraman and Khan, Maksudur R. (2015) Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania. Journal of Environmental Chemical Engineering. pp. 1-10. ISSN 2213-3437 http://dx.doi.org/10.1016/j.jece.2014.10.016 DOI: 10.1016/j.jece.2014.10.016
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
English
topic TP Chemical technology
spellingShingle TP Chemical technology
Cheng, C. K.
Mohd Rizauddin, Deraman
Khan, Maksudur R.
Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
description This paper reports the photocatalytic degradation of pre-treated palm oil mill effluent (POME) over a Pt-doped titania photocatalyst. Pt loading on the titania was varied from 0.25 to 1.0 wt% via alcohol reduction of chloroplatinic acid (H2PtCl6). XRD characterization of the photocatalysts showed that the photo-active anatase phase was still intact after the photocatalyst synthesis while the XPS spectrum confirmed that the deposited Pt was free from the Cl and existed as Pt0 and Pt4+. In addition, the UV–vis diffuse reflectance measurement indicated an improved light energy absorption in the visible light spectrum. Moreover, the band gap energy (3.16–3.17 eV) was reduced when titania was doped with Pt, compared to the pristine titania with 3.20 eV. The 0.5 wt% Pt/TiO2 photocatalyst offered the most effective degradation of pre-treated POME under the irradiation of 100 W of UV light (10%) and also visible light (11%), respectively, over a loading of 0.2 g/L. Significantly, the maximum 0.5 wt% Pt/TiO2 photocatalyst loading determined from the current work was 1.0 g/L.
format Article
author Cheng, C. K.
Mohd Rizauddin, Deraman
Khan, Maksudur R.
author_facet Cheng, C. K.
Mohd Rizauddin, Deraman
Khan, Maksudur R.
author_sort Cheng, C. K.
title Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
title_short Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
title_full Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
title_fullStr Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
title_full_unstemmed Evaluation of the Photocatalytic Degradation of Pre-Treated Palm Oil Mill Effluent (POME) Over Pt-Loaded Titania
title_sort evaluation of the photocatalytic degradation of pre-treated palm oil mill effluent (pome) over pt-loaded titania
publisher Elsevier Ltd
publishDate 2015
url http://umpir.ump.edu.my/id/eprint/7467/1/Evaluation_of_the_photocatalytic_degradation_of_pre-treated_palm_oil_mill_effluent_%28POME%29_over_Pt-loaded_titania.pdf
http://umpir.ump.edu.my/id/eprint/7467/4/Evaluation%20of%20the%20Photocatalytic%20Degradation%20of%20Pre-Treated%20Palm%20Oil%20Mill%20Effluent%20%28Pome%29%20Over%20Pt-Loaded%20Titania.pdf
http://umpir.ump.edu.my/id/eprint/7467/
http://dx.doi.org/10.1016/j.jece.2014.10.016
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