4.7 Article

Efficient mineralization of TBBPA via an integrated photocatalytic reduction/oxidation process mediated by MoS2/SnIn4S8 photocatalyst

期刊

CHEMOSPHERE
卷 285, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.131542

关键词

Photocatalytic reduction; Photocatalytic oxidation; Degradation; TBBPA; Metal sulfide photocatalysts

资金

  1. Open Project Program of Indoor environment engineering research center of Fujian Province (Fujian University of Technology) [KF-H19008]
  2. National Engineering Research Center for Environmental Photocatalysis (Fuzhou University) [201904]
  3. Initial Scientific Research Foundation of Fujian University of Technology [GYZ18063, GY-Z20014]

向作者/读者索取更多资源

A novel photocatalyst MoS2/SnIn4S8 was synthesized and employed for the remediation of TBBPA under visible light, demonstrating outstanding photocatalytic performance and stability, successfully reducing TBBPA to non-toxic substances.
Currently, Tetrabromobisphenol A (TBBPA) has been regarded as an emerging organic pollutant and efficient TBBPA elimination technology has been attracting increasing attention. In this work, a novel photocatalyst, MoS2/SnIn4S8, was synthesized through hydrothermal method by introducing few-layer MoS2 nanosheets and then employed to establish an integrated photocatalytic reduction/oxidation system for the remediation of TBBPA under visible light. The characterization results demonstrated that the few-layer MoS2 nanosheets were well combined with SnIn4S8 and significantly lowered the recombination rate of the photo-induced electron and holes, leading to outstanding photocatalytic performance of MoS2/SnIn4S8 composite. Besides, the MoS2/SnIn4S8 composite also exhibited excellent reusability (over 10 runs) and stability. The TBBPA degradation experiments showed that the integrated photocatalytic reduction/oxidation system was able to completely degrade TBBPA and mineralize its byproducts (60.2 +/- 2.9%). In the photocatalytic reduction, due to the cleavage of C-Br bonds by photo-induced electrons, TBBPA underwent stepwise debromination and finally transferred into BPA in 6 h. In the following photocatalytic oxidation, under the attack of reactive oxygen species (O-1(2), h(+), (OH)-O-center dot and O-center dot(2)-), BPA was first decomposed into aromatic products (such as phenol, benzoic acid, p-hydroxybenzyl alcohol and so on) via C-C bond cracking and hydroxylation, and then further oxidized into organic acids like maleic acid and muconic acid through ring-opening, and finally mineralized into CO2 and H2O. What was noteworthy was that the final effluent from the photocatalytic reduction/oxidation system showed no toxicity to the luminescent bacteria.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据