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TC-HCl
CHEMICAL PHYSICS · 2024 · IF 2

Synergistic photocatalytic degradation of TC-HCl by MIL-53(Fe)/CoWO4 composite and PMS under visible light

Qian Liu,Panpan Xu,Qianqian Zhang,Guangming Han,Ling Li,Limin Zhou

A series of novel MIL-53(Fe)/CoWO 4 composites were synthesized by combining MIL-53(Fe) and CoWO 4 nanoparticles via solvothermal method. The structural characterizations showed that CoWO 4 nanoparticles were uniformly distributed on the surface of hexagonal bipyramid MIL-53(Fe). Combining XPS and Mott-Schottky plots, a Z-scheme heterojunction was formed between MIL-53(Fe) and CoWO 4 , resulting in a significant improvement in the electron-hole pair separation efficiency. UV–vis diffused reflectance spectra indicated that the optical arrange of MIL-53(Fe)/CoWO 4 composites were expanded to visible light. The photocatalytic degradation experiments under visible light irradiation showed that MIL/CWO-60 synergistically with PMS degraded 90.5 % of TC-HCl within 50 min. The XRD spectra of used and unused composites were identical, indicating good stability in four consecutive cycles. Electron paramagnetic resonance (EPR) and free radicals trapping experiment revealed that active species included O 2− , SO 4 − , h + , OH and 1 O 2 , and mechanism of the synergistic degradation of TC-HCl by MIL-53(Fe)/CoWO 4 composites and PMS was proposed.

CAS / MDL: 299-11-6 64-75-5
研究领域: 环境科学 · 材料科学
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LANGMUIR · 2025 · IF 3.9

Highly Efficient Photocatalytic Degradation of TC-HCl by Morphology Regulation of Ga2O3 Nanostructures

Mingxin Ren,Jizhou Yang,Zhiyuan Chen,Zhi Wan,Peilin Zuo,Zhenghang Tian,Zhigang Liu,Feng Teng,Peng Hu,Haibo Fan

Tetracycline antibiotic contaminants have attracted more and more attention due to their high toxicity and the difficulty of their natural decomposition. Here, we have successfully regulated the morphologies of Ga2O3 photocatalysts (Ga2O3 QDs, Ga2O3 hollow spheres, and Ga2O3 micrometer rods) through a simple solvothermal and hydrothermal method and investigated their photocatalytic degradation of tetracycline hydrochloride (TC-HCl). It was found that Ga2O3 QDs showed the best photocatalytic performance due to their large specific surface area (61.1838 m2 g–1), wide bandgap (4.62 eV), etc. After the preparation conditions had been optimized, the Ga2O3 QDs synthesized at 240 °C and 10 h exhibited the best performance in degrading TC-HCl; after 500 W xenon lamp irradiation for 20 min, the degradation efficiency can reach 99% and the degradation rate reached 0.2988 min–1. By trapping experiments, the main active substances in the degradation of TC-HCl by Ga2O3 were identified as a superoxide radical (•O2) and a hole (h+). This study provides a new idea of catalyst morphology regulation and a new method for efficient photocatalytic degradation of TC-HCl.

研究领域: 环境化学 · 材料科学 · 光催化 · 纳米技术 · 污染物降解
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ENVIRONMENTAL RESEARCH · 2023 · IF 8.3

A new S-scheme heterojunction of 1D ZnGa2O4/ZnO nanofiber for efficient photocatalytic degradation of TC-HCl

Wenhui Chen,Tianxin Kang,Fenqi Du,Peipei Han,Meiling Gao,Peng Hu,Feng Teng,Haibo Fan

One-dimensional shaped ZnGa 2 O 4 , ZnO and ZnGa 2 O 4 /ZnO nanofibers were successfully prepared by electrostatic spinning technique and the photocatalytic degradation performance of tetracycline hydrochloride (TC-HCl) were studied. It was found that the S-scheme heterojunction formed in the ZnGa 2 O 4 /ZnO could greatly reduce the recombination of the photogenerated carriers and therefore improve the photocatalytic performance. By optimizing the ratio of the ZnGa 2 O 4 and ZnO, the largest degradation rate could reach 0.0573 min −1 , which was 20 times of the self-degradation rate of TC-HCl. It was verified that the h + played the key role in the reactive groups for the high performance decomposition of TC-HCl by capture experiments. This work provides a new method for the highly efficient photocatalytic degradation of TC-HCl.

CAS / MDL: 106-51-4 69365-72-6
研究领域: 环境科学 · 材料科学
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CURRENT APPLIED PHYSICS · 2022 · IF 2.856

High vis-light photocatalytic property of g-C3N4 on four pollutants (RhB, MB, TC-HCl and P-Nitrophenol)

Xiaoxue Lian,Yan Li,Yunling Zou,Dongmin An,Qiong Wang,Qingjun Zhou,Xueqi Li

The g-C 3 N 4 nanosheets were synthesized by a multistage program calcination with different heating rate, which was an easy, low-cost, and quick method. The morphology and structure of samples were characterized by various techniques. The performance evaluation of the samples was tested by degrading Rhodamine B, Methylene Blue, Tetracycline Hydrochloride and P-Nitrophenol in visible light . The results show that the photodegradation properties of TP-g-C 3 N 4 prepared by multistage program calcination are the best than others. In particular, the degradation rate of TP-g-C 3 N 4 to Rhodamine B reached 99.6% in just 4 min. TP-g-C 3 N 4 catalyst has excellent stability and recycling performance. According to free radical capture experiments, •O 2 − may be the main active species for pollutant degradation. The possible photocatalytic degradation mechanism was also discussed. Due to the high specific surface area and a narrow band gap, the TP-g-C 3 N 4 becomes a promising photocatalyst.

CAS / MDL: 57-13-6
研究领域: 材料科学 · 环境科学
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International Journal of Environmental Research and Public Health · 2022 ·Vol. 19 ·期 22 ·14935 · IF 4.614

2D/2D Phosphorus-Doped g-C3N4/Bi2WO6 Direct Z-Scheme Heterojunction Photocatalytic System for Tetracycline Hydrochloride (TC-HCl) Degradation

Xudong Yin,Xiaojie Sun,Dehao Li,Wenyu Xie,Yufeng Mao,Zhenghui Liu,Zhisen Liu

Bi2WO6-based heterojunction photocatalyst for antibiotic degradation has been a research hotspot, but its photocatalytic performance needs to be further improved. Therefore, 2D/2D P-doped g-C3N4/Bi2WO6direct Z-scheme heterojunction photocatalysts with different composition ratios were prepared through three strategies of phosphorus (P) element doping, morphology regulation, and heterojunction, and the efficiency of its degradation of tetracycline hydrochloride (TC-HCl) under visible light was studied. Their structural, optical, and electronic properties were evaluated, and their photocatalytic efficiency for TC-HCl degradation was explored with a detailed assessment of the active species, degradation pathways, and effects of humic acid, different anions and cations, and water sources. The 30% P-doped g-C3N4/Bi2WO6had the best photocatalytic performance for TC-HCl degradation. Its photocatalytic rate was 4.5-, 2.2-, and 1.9-times greater than that of g-C3N4, P-doped g-C3N4, and Bi2WO6, respectively. The improved photocatalytic efficiency was attributed to the synergistic effect of P doping and 2D/2D direct Z-scheme heterojunction construction. The stability and reusability of the 30% P-doped C3N4/Bi2WO6were confirmed by cyclic degradation experiments. Radical scavenging experiments and electron spin resonance spectroscopy showed that the main active species were •O2−and h+. This work provides a new strategy for the preparation of direct Z-scheme heterojunction catalysts with high catalytic performance.Keywords:P-doped g-C3N4;Bi2WO6;2D/2D direct Z-scheme heterojunction;photocatalytic degradation;tetracycline hydrochloride

CAS / MDL: 7647-01-0
研究领域: 环境科学 · 材料科学 · 化学工程 · 光催化
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NEW JOURNAL OF CHEMISTRY · 2019 ·Vol. 44 ·期 1 ·79-86 · IF 3.069

A 2D mesoporous photocatalyst constructed by the modification of biochar on BiOCl ultrathin nanosheets for enhancing the TC-HCl degradation activity

Yan Yan,Xu Tang,Changchang Ma,Hai Huang,Kesheng Yu,Yang Liu,Ziyang Lu,Chunxiang Li,Zhi Zhu,Pengwei Huo

In this paper, a two-dimensional (2D) photocatalyst by the BiOCl ultrathin nanosheet modification of biochar (derived from biomass bamboo leaves) was successfully prepared via a facile one-pot hydrothermal process. The synthesized C/BiOCl photocatalysts showed a satisfactory performance on the degradation of tetracycline hydrochloride (TC-HCl). The enhanced photocatalytic activity originating from the introduction of biochar facilitated the rapid transfer of electrons generated from the defect states of the BiOCl ultrathin nanosheets. Moreover, the more the photo-electrons transferred in biochar, the more the quantities of active ˙O2− generated during the photocatalytic reaction, which was confirmed from the free radical capture tests. This work can be extended to the modified routes of BiOCl in the further applications of environmental wastewater treatments.

CAS / MDL: 69-65-8
研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2023 · IF 5.2

Preparation of highly N-doped CoFeN by pyrolysis g-C3N4 for markedly enhanced Fenton degradation of MO and TC-HCl under visible illumination

Shihao Miao,Yuanguang Zhang,Hongyu Xia,Hongcheng Gao,Weihao Tao,Zhenzhu Zhang,Chenyu Huang,Lin Huang

In the study, highly N-doped metal organic framework (MOFs) derived CoFeN photocatalysts (CoFeN-N) were successfully prepared by using carbon nitride (g-C 3 N 4 ) nanosheets as the support with simultaneous additional N source. CoFeN-N activated hydrogen peroxide (H 2 O 2 ) was used to remove Methyl orange (MO) and Tetracycline hydrochloride (TC-HCl) in water under simulated visible light . N doping improves the photo-Fenton degradation ability of CoFeN to varying degrees, and the photocatalyst with the best performance is CoFeN-N2. The degradation rate constants (K) of MO and TC-HCl are 1.8 and 5.1 times of CoFeN, respectively. CoFeN-N2 did not significantly inhibit the degradation efficiency of organic pollutants under acidic, neutral and alkaline conditions. Meanwhile, the presence of coexisting anions (Cl − 、HCO 3 - and HPO 4 2- ) in water similarly does not obviously reduce the degradation ability of CoFeN-N2 for MO and TC-HCl, which indicates the excellent anti-interference ability of the prepared photocatalyst. The TOC test results indicate that CoFeN-N2 has excellent mineralization ability for organic contaminants. In addition, hydroxyl radicals , superoxide radicals, and holes (·OH, ·O 2 - and h + ) were demonstrated to be the primary active species for the degradation of organic pollutants by CoFeN-N2 through free radical trapping experiments and EPR tests. This work provides an attractive strategy for the preparation of highly N-doped photocatalysts and the efficient removal of organic pollutants from water by photo-Fenton coupling.

CAS / MDL: 64-75-5
研究领域: 环境科学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Synergistic SPR and IEF effects in Pt-modified 2D/2D BiOBr/Bi2WO6 S-scheme heterojunction for ultrafast degradation of organic pollutants

Jin Chen,Jiayu Lei,Jie Yan,Yuzhao Ma,Xiaofeng Yang,Yanjun Li

The establishment of a surface plasmon resonance (SPR) effect and an internal electric field (IEF) has been recognized as an effective technique for optimizing pollutant treatment in aquatic environments. Herein, we synthesized a novel 2D/2D Pt@BiOBr/Bi 2 WO 6 S-scheme heterojunction that establishes robust interfacial connections to enhance electron transport through minimized pathways, while simultaneously increasing active site availability. Subsequently, noble metal Pt was employed to modify the BiOBr/Bi 2 WO 6 composite material, thereby inducing SPR and broadening the light absorption range. Impressively, the optimized Pt@BiOBr/Bi 2 WO 6 demonstrates a significantly enhanced degradation efficiency for organic pollutants, primarily due to the synergistic effects of SPR and IEF. The degradation rate of tetracycline hydrochloride (TC-HCL) through the ternary heterojunction 2-PBB can achieve 100 % within 30 min under 500 W of visible light irradiation, showcasing impressive cyclic stability. Furthermore, the developed photocatalyst also demonstrated remarkable degradation efficiency for organic dyes such as Rhodamine B (RhB) and methyl orange (MO). This work demonstrates an original approach to the fabrication of Pt-modified S-scheme heterojunction photocatalysts with high effectiveness.

CAS / MDL: 18497-13-7 57-09-0
研究领域: 环境科学 · 光催化 · 材料科学 · 纳米技术 · 水处理
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