Active carbon/TiO2 composites for photocatalytic decomposition of benzoic acid in water and toluene in air

被引:9
作者
Pausova, S. [1 ]
Pacileo, L. [1 ]
Baudys, M. [1 ]
Hrubantova, A. [1 ]
Neumann-Spallart, M. [1 ]
Dvoranova, D. [2 ]
Brezova, V [2 ]
Krysa, J. [1 ]
机构
[1] Univ Chem & Technol, Dept Inorgan Technol, Tech 5, Prague 16628 6, Czech Republic
[2] Slovak Univ Technol Bratislava, Fac Chem & Food Technol, Inst Phys Chem & Chem Phys, Radlinskeho 9, SK-81237 Bratislava, Slovakia
关键词
Active carbon; Benzoic acid; Toluene; Adsorption; Photocatalytic oxidation; EPR spectroscopy; TIO2; DEGRADATION; ADSORPTION; REMOVAL;
D O I
10.1016/j.cattod.2020.06.048
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The present work describes the preparations of active carbon (AC) - titania composites with 2 different AC/TiO2 ratios, their characterization using SEM, BET, determination of particle size, and evaluation of adsorption ability and photocatalytic activity using benzoic acid (BA) in the aqueous phase and toluene in the gaseous phase. Composite materials based on AC/TiO2 were prepared from two types of active carbon (having a BET surface area of 1737 m(2) g(-1) and 890 m(2) g(-1), respectively) and TiO2 (P25, BET surface area 45 m(2) g(-1)) by mixing. The main studied parameter was milling of AC. Immobilized photocatalyst films were prepared by drop-casting of aqueous composite suspensions on glass substrates and drying. The composite films prepared from milled AC have much better adhesion to substrate in aqueous media than those from non-milled AC, which is due to a decrease of particle size by about 1 order during milling. The ability of composites prepared from milled AC to remove BA was more than 2.5 times higher than that of composites from non-milled AC. In comparison with TiO2, prepared composites showed similar or higher photocatalytic activity and the irradiation of AC/TiO2 composites in aqueous suspensions resulted in the generation of a comparable concentration of the hydroxyl radical spin-adduct ((DMPO)-D-center dot-OH) as with TiO2.
引用
收藏
页码:417 / 423
页数:7
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