四环素
海藻酸钠
兴奋剂
羧酸盐
X射线光电子能谱
四环素类抗生素
热液循环
材料科学
水热合成
核化学
原位
光催化
化学工程
钠
化学
立体化学
抗生素
催化作用
有机化学
生物化学
工程类
光电子学
作者
Zhancheng Zhang,Rongmin Wang,Junhui Guo,Yufeng He,Pengfei Song,Rongmin Wang
标识
DOI:10.1002/slct.201903827
摘要
Abstract 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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