Biomass guided the formation of spherical catalysts for efficient photodegradation of tetracycline hydrochloride

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
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引用次数: 0

Abstract

Developing and evaluating advanced antibiotic degradation photocatalysts remains challenging owing to the lack of rational structural designs and molecular oxygen activation. In this study, a nanofluoral-biochar-modified bismuth vanadate (m-BiVO4) material with a specific structure was prepared via surface-assisted polymerization. The results show that the yeast-derived carbon material significantly broadened the capture range of n–p* visible light and improved the electron delocalization and carrier separation rates. Under visible light irradiation, m-BiVO4 exhibited a high photocatalytic degradation rate, and the degradation rate of 10 mg/L tetracycline (TC) reached 89.9 % within 180 min, almost three times that of the control group. An EPR test and free radical capture experiment showed that ·OH and ·O2 were the main active substances in the TC degradation process. Cyclic experiments also showed that the material had great stability and potential for reuse. The intermediate in the degradation pathway was identified using liquid chromatography-tandem mass spectrometry, the degradation pathway of TC in the composite system was predicted, and a corresponding degradation pathway was proposed. In this study, the synergistic effect of morphology adjustment and component cutting was realized using biomass templates, providing a new method for designing photocatalysts with specific structures.

生物质引导形成高效光降解盐酸四环素的球形催化剂
由于缺乏合理的结构设计和分子氧活化,开发和评估先进的抗生素降解光催化剂仍具有挑战性。本研究通过表面辅助聚合法制备了一种具有特定结构的纳米芴-生物炭修饰钒酸铋(m-BiVO4)材料。结果表明,酵母衍生碳材料显著拓宽了 n-p* 可见光的捕获范围,提高了电子析出率和载流子分离率。在可见光照射下,m-BiVO4 表现出较高的光催化降解率,在 180 分钟内对 10 mg/L 四环素(TC)的降解率达到 89.9%,几乎是对照组的三倍。EPR 测试和自由基捕获实验表明,-OH 和 -O2- 是 TC 降解过程中的主要活性物质。循环实验还表明,该材料具有很高的稳定性和再利用潜力。利用液相色谱-串联质谱鉴定了降解途径中的中间体,预测了 TC 在复合体系中的降解途径,并提出了相应的降解途径。该研究利用生物质模板实现了形态调整和组分切割的协同效应,为设计具有特定结构的光催化剂提供了一种新方法。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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