In Situ Synthesis of C–Doped BiOBr Micron‐Flower by Structural Induction of Sodium Alginate for Rapid Removal Tetracycline | Zendy

Zhang Zhancheng | Zendy; Wang Bin | Zendy; Guo Junhui | Zendy; He Yufeng | Zendy; Song Pengfei | Zendy; Wang Rongmin | Zendy

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In Situ Synthesis of C–Doped BiOBr Micron‐Flower by Structural Induction of Sodium Alginate for Rapid Removal Tetracycline

Author(s) -

Zhang Zhancheng,

Wang Bin,

Guo Junhui,

He Yufeng,

Song Pengfei,

Wang Rongmin

Publication year - 2019

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.201903827

Subject(s) - tetracycline , sodium alginate , doping , carboxylate , x ray photoelectron spectroscopy , tetracycline antibiotics , hydrothermal circulation , materials science , hydrothermal synthesis , nuclear chemistry , in situ , photocatalysis , chemical engineering , sodium , chemistry , stereochemistry , antibiotics , catalysis , organic chemistry , biochemistry , optoelectronics , engineering

C‐doped into the BiOBr is a big challenge because unique lattice structure. Here, using sodium alginate (SA) as the structure‐directing agent and C source, the C‐doped BiOBr micron‐flower (BiOBr‐SA) was in‐situ synthesized with KBr and Bi(NO 3 ) 3 with hydrothermal, and characterized by XRD, SEM, XPS, BET and DRS. It was found that SA could control morphology of BiOBr‐SA as it contains carboxylate groups. Meanwhile, C−Bi bonds were formed in nanosheets, and further self‐assembled into BiOBr‐SA micron‐flower. Using BiOBr‐SA as photocatalyst for degradation of antibiotic and dye, the removal rate of tetracycline got to 88.7%.

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