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Investigation efficiency of nano photocatalytic compound of TiO2 and rice husk silica in removal of reactive red 198 dye from synthetic aqueous solutions | ||
Iranian Journal of Catalysis | ||
مقاله 3، دوره 10، شماره 1، خرداد 2020، صفحه 23-32 اصل مقاله (1.28 M) | ||
نوع مقاله: Articles | ||
نویسندگان | ||
Abdollrahman Mahmoodi1؛ Seyed Mahmood Mehdinia2؛ Ayat Rahmani1؛ Hamidreza Nassehinia* 1 | ||
1Department of Environmental Health Engineering, Semnan University of Medical Sciences, Semnan, Iran. | ||
2Department of Environmental Health Engineering, Babol University of Medical Sciences, Babol, Iran. | ||
چکیده | ||
This study was performed with the aim of investigating the efficiency of the Nano photocatalytic of ultraviolet and titanium dioxide compound and rice husk silica adsorbent (UV/TiO2/RHS) in removal reactive red 198 dye from synthetic aqueous solutions. The removal of reactive red 198 dye was done in batch reactors with a volume of 250 ml using RHS deposited by titanium dioxide in the presence of a UV lamp. The effect of pH, immobilization of TiO2 on RHS adsorbent, contact time, nanoparticle mass and initial concentration of dye in removal efficiency were investigated. The results of this research showed that with an increase in pH and alkalinity of the solution, the removal efficiency declined. As the pH changed from 3 to 9, the removal efficiency in UV/TiO2/RHS, RHS adsorbent and UVC radiation declined from 75.25 to 27.87, 8.37 to 3.4, and 16.62 to 3.25%, respectively. The maximum dye removal efficiency obtained by UV/TiO2/RHS was as large as 87.5% under pH=3, contact time of 60 min, nanoparticle mass of 1 g/L, and 25 mg/L concentration of the reactive red 198 dye. Therefore, the rice husk silica as a natural adsorbent in combination with (TiO2/UV) can be used as an effective method for removal reactive red of aqueous solutions on a larger scale by optimizing the parameters affecting the removal efficiency. | ||
کلیدواژهها | ||
Photocatalyst؛ Rice husk silica؛ Reactive red 198؛ Removal efficiency | ||
مراجع | ||
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