Loading…

Novel Removal of Diazinon Pesticide by Adsorption and Photocatalytic Degradation of Visible Light-Driven Fe-TiO2/Bent-Fe Photocatalyst

In the study, Fe was used as a dopant to enhance photocatalytic activity of TiO2. Then, the Fe-doped TiO2 was deposited on bentonite, which was pillared by Fe. The synthesized materials were characterized by SEM, XRD, UV-Vis, BET, and point of zero charge (pHPZC). Then, the synthesized materials wer...

Full description

Saved in:
Bibliographic Details
Published in:Journal of chemistry 2019-01, Vol.2019 (2019), p.1-7
Main Authors: Thanh Truc, Nguyen Thi, Van Quan, Pham, Viet, Huong Do Thi, Hanh, Nguyen Thi, Ha, Minh Ngoc, Van Thuan, Doan, Chu, Ngoc Chau, Phuong, Nguyen Minh, Minh Thu, Nguyen Thi
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In the study, Fe was used as a dopant to enhance photocatalytic activity of TiO2. Then, the Fe-doped TiO2 was deposited on bentonite, which was pillared by Fe. The synthesized materials were characterized by SEM, XRD, UV-Vis, BET, and point of zero charge (pHPZC). Then, the synthesized materials were used for diazinon removal under both dark and visible light conditions to investigate adsorption and photocatalytic degradation abilities of the synthesized materials. The maximum diazinon adsorption capacity of the synthesized Fe-TiO2/Bent-Fe was 27.03 mg/g. The obtained results indicated that the Fe-TiO2/Bent-Fe exhibited high photocatalytic degradation activity for removal of diazinon even under visible light. The diazinon removal experiments were also conducted using different photocatalyst dosages, under different pH and light sources to figure the optimal conditions for removal processes. The obtained results indicated that optimal photocatalyst dosage and pH were 0.5 g/L and 4.5, respectively. Finally, the natural light generated from solar could be suitable used for diazinon removal by the synthesized Fe-TiO2/Bent-Fe.
ISSN:2090-9063
2090-9071
DOI:10.1155/2019/2678927