scholarly journals Photocatalytic degradation of Direct Yellow-27 by photolysis with UV-light and solar irradiation Using N-doped TiO2

2019 ◽  
Vol 1 (2) ◽  
pp. 62
Author(s):  
Deliza . ◽  
Safni . ◽  
Diana Vanda Wellia ◽  
Toyohide Takeuchi

.

2017 ◽  
Vol 88 ◽  
pp. 200-206 ◽  
Author(s):  
Behzad Shahmoradi ◽  
Mohammad Amin Pordel ◽  
Meghdad Pirsaheb ◽  
Afshin Maleki ◽  
Shadi Kohzadi ◽  
...  

2011 ◽  
Vol 214 ◽  
pp. 40-44
Author(s):  
Hong Li ◽  
Qian Li ◽  
Wen Jie Zhang

A porous SiO2-doped TiO2 photocatalyst was prepared through co-sol-gel method used for photocatalytic degradation of methyl orange. PEG1000 was used as a template. Photocatalytic degradation was conducted after adsorption equilibrium to identify the contribution of both adsorption and photocatalytic degradation. While PEG addition ranged from 0.25 g to 1.0 g, the optimum addition amount was at 0.5 g. The degradation rate increased with increasing calcination temperature in the range from 400 to 500 oC, and then it decreased with still increasing temperature. The photocatalyst calcinated at 500 oC for 4 h could degrade 29.2% of the initial methyl orange in 30 min. Nearly 96.5% of decoloration of the initial methyl orange was removed in 100 min under UV light irradiation with the existence of the porous SiO2-doped TiO2.


2016 ◽  
Vol 13 (1) ◽  
pp. 110-116 ◽  
Author(s):  
Rani P. Barkul ◽  
Farah-Naaz A. Shaikh ◽  
Sagar D. Delekar ◽  
Meghshyam K. Patil

Materials ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1338 ◽  
Author(s):  
Klara Perović ◽  
Francis M. dela Rosa ◽  
Marin Kovačić ◽  
Hrvoje Kušić ◽  
Urška Lavrenčič Štangar ◽  
...  

Clean water and the increased use of renewable energy are considered to be two of the main goals in the effort to achieve a sustainable living environment. The fulfillment of these goals may include the use of solar-driven photocatalytic processes that are found to be quite effective in water purification, as well as hydrogen generation. H2 production by water splitting and photocatalytic degradation of organic pollutants in water both rely on the formation of electron/hole (e−/h+) pairs at a semiconducting material upon its excitation by light with sufficient photon energy. Most of the photocatalytic studies involve the use of TiO2 and well-suited model compounds, either as sacrificial agents or pollutants. However, the wider application of this technology requires the harvesting of a broader spectrum of solar irradiation and the suppression of the recombination of photogenerated charge carriers. These limitations can be overcome by the use of different strategies, among which the focus is put on the creation of heterojunctions with another narrow bandgap semiconductor, which can provide high response in the visible light region. In this review paper, we report the most recent advances in the application of TiO2 based heterojunction (semiconductor-semiconductor) composites for photocatalytic water treatment and water splitting. This review article is subdivided into two major parts, namely Photocatalytic water treatment and Photocatalytic water splitting, to give a thorough examination of all achieved progress. The first part provides an overview on photocatalytic degradation mechanism principles, followed by the most recent applications for photocatalytic degradation and mineralization of contaminants of emerging concern (CEC), such as pharmaceuticals and pesticides with a critical insight into removal mechanism, while the second part focuses on fabrication of TiO2-based heterojunctions with carbon-based materials, transition metal oxides, transition metal chalcogenides, and multiple composites that were made of three or more semiconductor materials for photocatalytic water splitting.


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