Carboxylate-functionalized polyoxo-titanium clusters for adsorption/solar photocatalytic synergistic tetracycline degradation†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2025-01-23 DOI:10.1039/D4TA08391A
Shu-Han Wang, Ming Du, Hui-Li Guo, Hui-Yuan Chen, Jing-Yu Pang, Dong-Bin Dang and Yan Bai
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Abstract

Adjusting the bandgap of polyoxo-titanium clusters (PTCs) to enhance their visible light catalytic performance is one of the effective strategies. Herein, three PTCs modified by organic carboxylic acid ligands with different conjugated systems were synthesized in one-step, [Ti6(O3P-Phen)2(OiPr)10(L)2] (OiPr = isopropyl alcohol; L = benzimidazole dicarboxylic acid, Ti6-BIDC; 4-chloromethyl benzoic acid = CMBA, Ti6-CMBA; malonic acid = MA, Ti6-MA), and were used as photocatalysts in the visible light catalytic degradation of tetracycline (50 mL, 50 mg L−1). Ti6-BIDC showed excellent catalytic activity and cycling stability in the degradation of tetracycline. Importantly, the degradation efficiency under real sunlight was 92.4%. The modification of carboxylic acid ligands significantly changed the photoelectric properties and specific surface area of the compounds. In addition, the results of active species trapping experiments demonstrated that the superoxide anion (˙O2) radical and hole (h+) played dominant roles in TC degradation. The intermediates and possible pathways of TC degradation were analyzed by LC-MS, and the toxicity of the degradation intermediates was evaluated by the Mung bean planting experiment and toxicity estimation software tool (T.E.S.T.). This is the first report on the application of PTCs in photocatalytic degradation of tetracycline, providing new ideas for the degradation of tetracycline.

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羧酸功能化多氧钛团簇吸附/太阳能光催化协同降解四环素
调整多氧钛团簇(ptc)的带隙以提高其可见光催化性能是有效的策略之一。本文一步合成了三种由不同共轭体系的有机羧酸配体修饰的ptc, [Ti6(O3P-Phen)2(OiPr)10(L)2] (OiPr =异丙醇;L =苯并咪唑二羧酸Ti6-BIDC;4-氯甲基苯甲酸= CMBA, Ti6-CMBA;丙二酸= MA, Ti6-MA),作为可见光催化降解四环素(50 mL, 50 mg L−1)的光催化剂。Ti6-BIDC对四环素的降解具有良好的催化活性和循环稳定性。重要的是,在真实阳光下的降解效率为92.4%。羧酸配体的修饰显著改变了化合物的光电性能和比表面积。此外,活性物种捕获实验结果表明,超氧阴离子(˙O2−)自由基和空穴(h+)在TC降解中起主导作用。采用LC-MS分析了TC降解中间体和可能的降解途径,并通过绿豆种植试验和毒性评价软件(T.E.S.T.)对降解中间体的毒性进行了评价。本文首次报道了ptc在四环素光催化降解中的应用,为四环素的降解提供了新的思路。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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