Hydrothermal assisted synthesis of titanium dioxide nanoparticles modified graphene with enhanced photocatalytic performance

被引:20
|
作者
Fadillah, Ganjar [1 ,2 ]
Hidayat, Rahmat [3 ]
Saleh, Tawfik A. [4 ]
机构
[1] Univ Islam Indonesia, Dept Chem, Yogyakarta 55584, Indonesia
[2] Kumamoto Univ, Dept Chem, Kumamoto 8608555, Japan
[3] Politekn Negeri Lampung, Dept Agr Technol, Lampung 35142, Indonesia
[4] King Fahd Univ Petr & Mineral, Dept Chem, Dhahran 31261, Saudi Arabia
关键词
Hydrothermal assisted green synthesis; TiO2; nanoparticles; Photocatalytic activity; INDIGO CARMINE; OXIDE NANOCOMPOSITES; AQUEOUS-SOLUTION; METHYLENE-BLUE; DEGRADATION; PHOTODEGRADATION; CATALYST; DYE;
D O I
10.1016/j.jiec.2022.06.016
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Water purification is a global issue, and most traditional methods have several drawbacks. As a result, new methods and materials must be devised to address the problem of water filtration. The hydrophobic TiO2-ZnO/rGO has been synthesized via single-step hydrothermal methods for the efficiency and effective indigo carmine (IC) solution degradation. The characterization of hydrophobic TiO2-ZnO/rGO has shown that the material has a high contact angle value of around 103.6 & DEG;. Several photocatalytic parameters, pH of IC solution, the dosage of catalyst, and light intensity, were optimized for obtaining the highest degradation efficiency. The results of the photocatalytic study showed that the IC dye degradation process was controlled by superoxide anion radical (.O-2(-) radicals) to produce more specific products. Modifications with hydrophobic compounds such as hexamethyldisilizane (HDMS) showed that they could increase the photocatalytic properties and reusability of the material with a degradation percentage value of up to 95% with a constant rate of 0.0361 min -1. Based on these results, this material has the potential to be further developed for micro and complex photodegradation and self-cleaning materials. (C) 2022 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:411 / 418
页数:8
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