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用于高效降解盐酸四环素的TiO-蛋壳结构构建:阳光诱导原位生成碳酸根自由基

Construction of TiO-Eggshell for Efficient Degradation of Tetracycline Hydrochloride: Sunlight Induced In-Situ Formation of Carbonate Radical.

作者信息

Huang Zhuquan, Wang Jiaqi, Yang Min-Quan, Qian Qingrong, Liu Xin-Ping, Xiao Liren, Xue Hun

机构信息

College of Environmental Science and Engineering, Fujian Normal University, Fuzhou 350007, China.

Fujian Key Laboratory of Pollution Control & Resource Reuse, Fujian Normal University, Fuzhou 350007, China.

出版信息

Materials (Basel). 2021 Mar 25;14(7):1598. doi: 10.3390/ma14071598.

Abstract

Photocatalytic degradation of an antibiotic by utilizing inexhaustible solar energy represents an ideal solution for tackling global environment issues. The target generation of active oxidative species is highly desirable for the photocatalytic pollutants degradation. Herein, aiming at the molecular structure of tetracycline hydrochloride (TC), we construct sunlight-activated high-efficient catalysts of TiO-eggshell (TE). The composite ingeniously utilizes the photoactive function of TiO and the composition of eggshell, which can produce oxidative ·CO species that are especially active for the degradation of aromatic compounds containing phenol or aniline structures. Through the synergistic oxidation of the··CO with the traditional holes (h), superoxide radicals (·O) and hydroxyl radicals (·OH) involved in the photocatalytic process, the optimal TE photocatalyst degrades 92.0% TC in 30 min under solar light, which is higher than TiO and eggshell. The photocatalytic degradation pathway of TC over TE has been proposed. The response surface methodology is processed by varying four independent parameters (TC concentration, pH, catalyst dosage and reaction time) on a Box-Behnken design (BBD) to optimize the experimental conditions. It is anticipated that the present work can facilitate the development of novel photocatalysts for selective oxidation based on ·CO.

摘要

利用取之不尽的太阳能光催化降解抗生素是解决全球环境问题的理想方案。光催化降解污染物时,非常需要有针对性地生成活性氧化物种。在此,针对盐酸四环素(TC)的分子结构,我们构建了阳光激活的高效TiO-蛋壳(TE)催化剂。该复合材料巧妙地利用了TiO的光活性功能和蛋壳的成分,能够产生对含有苯酚或苯胺结构的芳香族化合物降解特别活跃的氧化·CO物种。通过·CO与光催化过程中涉及的传统空穴(h)、超氧自由基(·O)和羟基自由基(·OH)的协同氧化作用,最优的TE光催化剂在太阳光下30分钟内可降解92.0%的TC,这比TiO和蛋壳的降解率更高。本文还提出了TC在TE上的光催化降解途径。通过在Box-Behnken设计(BBD)上改变四个独立参数(TC浓度、pH值、催化剂用量和反应时间)来处理响应面方法,以优化实验条件。预计本工作能够推动基于·CO的新型选择性氧化光催化剂的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99cb/8036644/39f3ca77ff77/materials-14-01598-g001.jpg

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