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Novel Magnetic Fe3O4/α-FeOOH Nanocomposites and Their Enhanced Mechanism for Tetracycline Hydrochloride Removal in the Visible Photo-Fenton Process.

ABSTRACT: Magnetic Fe3O4/α-FeOOH heterojunction nanocomposites (denoted as Fe-NCs) have been synthesized by a fast one-pot hydrothermal method. The obtained Fe-NCs contain rich micropores with a high surface area of 135.15 m2/g. The different phases in the composites can efficiently enhance the visible-light absorption, improving the separation and transfer of photogenerated electron-hole pairs during the photocatalytic reaction. Thus, they show excellent degradation and mineralization of tetracycline (TC) over a wide pH range (5-9) in the visible photo-Fenton reaction. Especially, the catalyst exhibits the highest adsorption capacity toward TC at a neutral pH, which facilitates the surface reactions of TC with active species. Experiments evidence that the high production of photogenerated holes and superoxide radicals (O2 •-) in Fe-NCs are favorable to the high catalytic efficiency. Combined with liquid chromatography-mass spectrometry, the possible pathway toward TC degradation was proposed.

SUBMITTER: Huang X 

PROVIDER: S-EPMC8028166 | biostudies-literature | 2021 Apr

REPOSITORIES: biostudies-literature

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Novel Magnetic Fe<sub>3</sub>O<sub>4</sub>/α-FeOOH Nanocomposites and Their Enhanced Mechanism for Tetracycline Hydrochloride Removal in the Visible Photo-Fenton Process.

Huang Xinyi X   Zhou Hui H   Yue Xiaojun X   Ran Songlin S   Zhu Jianhua J  

ACS omega 20210326 13

Magnetic Fe<sub>3</sub>O<sub>4</sub>/α-FeOOH heterojunction nanocomposites (denoted as Fe-NCs) have been synthesized by a fast one-pot hydrothermal method. The obtained Fe-NCs contain rich micropores with a high surface area of 135.15 m<sup>2</sup>/g. The different phases in the composites can efficiently enhance the visible-light absorption, improving the separation and transfer of photogenerated electron-hole pairs during the photocatalytic reaction. Thus, they show excellent degradation and m  ...[more]

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