期刊论文详细信息
Molecules
Photocatalytic Activity of Fibrous Ti/Ce Oxides Obtained by Hydrothermal Impregnation of Short Flax Fibers
Nikolay L. Ovchinnikov1  Mikhail F. Butman1  Karl W. Krämer2  Nataliya E. Kochkina3 
[1]Department of Ceramics Technology and Nanomaterials, Ivanovo State University of Chemistry and Technology, Sheremetevsky Avenue 7, 153000 Ivanovo, Russia
[2]Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland
[3]G.A. Krestov Institute of Solution Chemistry of Russian Academy of Sciences, Akademicheskaya St. 1, 153045 Ivanovo, Russia
关键词: Ti/Ce oxides;    Ti/Ce polyhydroxy complexes;    photocatalytic activity;   
DOI  :  10.3390/molecules26113399
来源: DOAJ
【 摘 要 】
Fibrous Ti/Ce oxide photocatalysts were prepared for the first time by a biomimetic solution process using short flax fibers (flax straw processing waste) as a biotemplate. Titanium polyhydroxy complex solutions with 3% and 5% cerium were used as precursors. Flax fibers were impregnated in an autoclave under hydrothermal conditions. Ti/Ce oxides were obtained from the biotemplate by annealing at 600 °C. The photocatalytic activity of the Ti/Ce oxides was studied by the adsorption and decomposition of the dye rhodamine B under UV irradiation. The photocatalytic decomposition of the dye was 50% and 75% faster for Ti/Ce oxides with 3% and 5% Ce, respectively, than for the analogous undoped fibrous TiO2. The morphologies, textures, and structures of the photocatalysts were studied by scanning electron microscopy, low temperature N2 adsorption/desorption, UV-Vis spectroscopy, and X-ray and XPS analytical methods. It was shown that the introduction of Ce into the precursor solution increased the surface irregularity of the Ti/Ce oxide crystallites compared to pure TiO2. This effect scaled with the Ce concentration. Ce improved the UV light absorption of the material. The Ti/Ce oxides contained Ce4+/Ce3+ pairs that played an important role in redox processes and intensified the photocatalytic activity.
【 授权许可】

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