Enhanced photodegradation of acetaminophen over Sr@TiO2/UiO-66-NH2 heterostructures under solar light irradiation

被引:34
|
作者
Wang, Y. L. [1 ]
Penas-Garzon, M. [1 ]
Rodriguez, J. J. [1 ]
Bedia, J. [1 ]
Belver, C. [1 ]
机构
[1] Univ Autonoma Madrid, Chem Engn Dept, Campus Cantoblanco, E-28049 Madrid, Spain
关键词
Sr@TiO2/UiO-66-NH2; Photocatalytic degradation; Acetaminophen; Continuous reaction; Solar light; METAL-ORGANIC-FRAMEWORKS; PHOTOCATALYTIC DEGRADATION; TIO2; UIO-66-NH2; POTENTIALS; ADSORPTION; POLLUTANTS; STRATEGIES;
D O I
10.1016/j.cej.2022.137229
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Novel Sr@TiO2/UiO-66-NH2 heterostructures were synthesized by a two-step solvothermal approach and tested as photocatalysts for the solar degradation of acetaminophen. Strontium titanate was used as precursor to obtain the heterostructures, resulting in Sr@TiO2 anchored and dispersed on the UiO-66-NH2. The effect of the Sr@TiO2:UiO-66-NH2 ratio was analyzed. All the heterostructures were more active than the pattern UiO-66NH(2), and the most active achieved more than 90% of conversion of acetaminophen. This enhanced degradation was ascribed to a better separation and faster transfer of charges, as confirmed by photoluminescence and electrochemical characterization. Radical trapping experiments revealed that superoxide radicals (O-2(center dot-)) and to a lower extent photoinduced holes (h(+)) were involved in acetaminophen degradation. As a novelty, the activity and stability of the best photocatalyst were evaluated in a continuous flow reaction system, upgrading conventional short-cycle batch studies. The heterostructure maintained an almost constant high conversion of acetaminophen during the 10 h on stream of the experiment, demonstrating excellent photocatalytic performance and stability in water. Besides, the photocatalytic degradation intermediates were identified, and a corresponding pathway of ACE transformation was proposed.
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页数:12
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