CuFeS 2 @Zn复合材料增强光催化降解Cr(VI)和土霉素

S. Vigneswaran , P. Gowthaman , S. Sangeethavanathi
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引用次数: 0

摘要

重金属和抗生素引起的水污染是一个重大的全球性挑战,需要制定有效的修复策略。在本研究中,将锌(Zn)掺杂CuFeS2(铜铁硫化物)复合材料作为可见光下降解六价铬(Cr(VI))和土霉素(OTC)的高效光催化剂。在不同Zn掺杂浓度(1 mol%、5 mol%和10 mol%)下,采用水热法合成了复合材料。采用x射线衍射、场发射扫描电镜、傅里叶变换红外光谱和紫外可见光谱对合成的复合材料进行了表征。x射线光电子能谱和布鲁诺尔-埃米特-泰勒分析揭示了它们的结构、形态、光学和表面积特性。其中,10 mol% CuFeS@Zn复合材料的降解效率最高,在100 min内达到99 % Cr(VI)和OTC的去除率,显著优于CuFeS 2、CuFeS 2 @Zn 1 mol%和CuFeS 2 @Zn 5 mol%复合材料。动力学分析表明,反应速率常数为3.041 min−1,在pH为6、催化剂用量为6 mg的条件下,CuFeS 2 @Zn为10 mol%,具有良好的光催化活性,多次循环后具有良好的可回收性和稳定性。锌的加入改善了载流子的分离和转移,促进了催化剂与污染物界面的氧化还原反应,从而提高了光催化性能。该研究为锌掺杂CuFeS 2复合材料的设计提供了有价值的见解,为开发用于环境修复的先进光催化材料提供了有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced photocatalytic degradation of Cr(VI) and oxytetracycline using CuFeS₂@Zn composites

Enhanced photocatalytic degradation of Cr(VI) and oxytetracycline using CuFeS₂@Zn composites
Water pollution caused by heavy metals and antibiotics poses a significant global challenge, necessitating the development of efficient remediation strategies. In this study, zinc (Zn) doped CuFeS2 (copper iron sulfide) composites were used as highly efficient photocatalysts for the degradation of hexavalent chromium (Cr(VI)) and oxytetracycline (OTC) under visible light. The composites were synthesized using a facile hydrothermal method with various Zn doping concentrations (1 mol%, 5 mol%, and 10 mol%). The synthesized composites were comprehensively characterized by X-ray diffraction, field-emission scanning electron microscopy, Fourier-transform infrared spectroscopy, and Ultraviolet-Visible spectroscopy. X-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller analysis revealed their structural, morphological, optical, and surface area properties. Among the composites, 10 mol% CuFeS@Zn exhibited the highest degradation efficiency, achieving 99 % Cr(VI) and OTC removal within 100 min. This performance significantly surpasses the efficiencies of CuFeS₂, and the CuFeS₂@Zn 1 mol%, and CuFeS₂@Zn 5 mol% composites. Kinetic analysis revealed a high reaction rate constant of 3.041 min1, and optimal photocatalytic activity was observed at pH 6 and a catalyst dosage of 6 mg, with excellent recyclability and stability demonstrated over multiple cycles for the CuFeS₂@Zn 10 mol% composite. The enhanced photocatalytic performance was attributed to the improved charge carrier separation and transfer resulting from Zn incorporation, which facilitated redox reactions at the catalyst-pollutant interface. This study provides valuable insights into the design of Zn-doped CuFeS₂ composites offering a promising pathway for the development of advanced photocatalytic materials for environmental remediation.
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