TiO2-coated mesoporous carbon: Conventional vs. microwave-annealing process

被引:28
作者
Coromelci-Pastravanu, Cristina [1 ]
Ignat, Maria [1 ,2 ]
Popovici, Evelini [1 ]
Harabagiu, Valeria [2 ]
机构
[1] Alexandru Ioan Cuza Univ, Dept Chem, Lab Mat Chem, Iasi 700506, Romania
[2] Petru Poni Inst Macromol Chem, Iasi 700487, Romania
关键词
Conventional heating; Microwaves; Composite photocatalyst; Improved photoactivity; PHOTOCATALYTIC DEGRADATION; OPTICAL-PROPERTIES; TITANIUM-DIOXIDE; METHYLENE-BLUE; TIO2; DYE; SOL; GLYCEROL;
D O I
10.1016/j.jhazmat.2014.06.036
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The study of coating mesoporous carbon materials with titanium oxide nanoparticles is now becoming a promising and challenging area of research. To optimize the use of carbon materials in various applications, it is necessary to attach functional groups or other nanostructures to their surface. The combination of the distinctive properties of mesoporous carbon materials and titanium oxide is expected to be applied in field emission displays, nanoelectronic devices, novel catalysts, and polymer or ceramic reinforcement. But, their synthesis is still largely based on conventional techniques, such as wet impregnation followed by chemical reduction of the metal nanoparticle precursors, which takes time and money. The thermal heating based techniques are time consuming and often lack control of particle size and morphology. Hence, since there is a growing interest in microwave technology, an alternative way of power input into chemical reactions through dielectric heating is the use of microwaves. This work is focused on the advantages of microwave-assisted synthesis of TiO2-coated mesoporous carbon over conventional thermal heating method. The reviewed studies showed that the microwave-assisted synthesis of such composites allows processes to be completed within a shorter reaction time allowing the nanoparticles formation with superior properties than that obtained by conventional method. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:382 / 390
页数:9
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