Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide
The photocatalytic activity of methyl orange (MO) in aqueous solution was studied using the hydrothermal synthesis of activated carbon-loaded TiO2 at different weight ratios. The hydrothermal process was conducted at a temperature of 180°C for 12 h in order to obtain a high surface area and porosity...
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Taylor & Francis
2016
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my.um.eprints.184302018-10-19T03:41:04Z http://eprints.um.edu.my/18430/ Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide Bagheri, Samira Mohd Hir, Z.A. Termeh Yousefi, A. Hamid, Sharifah Bee Abd Q Science (General) TA Engineering (General). Civil engineering (General) The photocatalytic activity of methyl orange (MO) in aqueous solution was studied using the hydrothermal synthesis of activated carbon-loaded TiO2 at different weight ratios. The hydrothermal process was conducted at a temperature of 180°C for 12 h in order to obtain a high surface area and porosity for the purpose of degradation activity. The results indicated that TiO2-PEG-Ac (0.50%) exhibited better photocatalytic performance compared to other prepared photocatalysts. The photodegradation process was observed to be pH dependent, since almost 100% of MO removal was possible in an acidic medium. In contrast, the degradation activity seems to be diminished in basic media. The overall photocatalytic activity of TiO2 was enhanced due to the presence of porous activated carbon as co-catalyst and support. Taylor & Francis 2016 Article PeerReviewed Bagheri, Samira and Mohd Hir, Z.A. and Termeh Yousefi, A. and Hamid, Sharifah Bee Abd (2016) Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide. Desalination and Water Treatment, 57 (23). pp. 10859-10865. ISSN 1944-3994 https://doi.org/10.1080/19443994.2015.1038593 doi:10.1080/19443994.2015.1038593 |
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Q Science (General) TA Engineering (General). Civil engineering (General) |
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Q Science (General) TA Engineering (General). Civil engineering (General) Bagheri, Samira Mohd Hir, Z.A. Termeh Yousefi, A. Hamid, Sharifah Bee Abd Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| description |
The photocatalytic activity of methyl orange (MO) in aqueous solution was studied using the hydrothermal synthesis of activated carbon-loaded TiO2 at different weight ratios. The hydrothermal process was conducted at a temperature of 180°C for 12 h in order to obtain a high surface area and porosity for the purpose of degradation activity. The results indicated that TiO2-PEG-Ac (0.50%) exhibited better photocatalytic performance compared to other prepared photocatalysts. The photodegradation process was observed to be pH dependent, since almost 100% of MO removal was possible in an acidic medium. In contrast, the degradation activity seems to be diminished in basic media. The overall photocatalytic activity of TiO2 was enhanced due to the presence of porous activated carbon as co-catalyst and support. |
| format |
Article |
| author |
Bagheri, Samira Mohd Hir, Z.A. Termeh Yousefi, A. Hamid, Sharifah Bee Abd |
| author_facet |
Bagheri, Samira Mohd Hir, Z.A. Termeh Yousefi, A. Hamid, Sharifah Bee Abd |
| author_sort |
Bagheri, Samira |
| title |
Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| title_short |
Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| title_full |
Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| title_fullStr |
Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| title_full_unstemmed |
Photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| title_sort |
photocatalytic performance of activated carbon-supported mesoporous titanium dioxide |
| publisher |
Taylor & Francis |
| publishDate |
2016 |
| url |
http://eprints.um.edu.my/18430/ https://doi.org/10.1080/19443994.2015.1038593 |
| _version_ |
1643690703552774144 |
| score |
13.251813 |