从藻类生物质中提取的 N 掺杂碳纳米片-镍铁氧体复合材料对抗生素的光催化降解。

Chemosphere Pub Date : 2024-09-01 Epub Date: 2024-07-20 DOI:10.1016/j.chemosphere.2024.142908
Shyamalee Patar, Rishi Mittal, Farishta Yasmin, Balin Kumar Bhuyan, Lakhya Jyoti Borthakur
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引用次数: 0

摘要

本研究报告采用溶热法合成了镍铁氧体(NiFe)纳米颗粒、掺氮介孔碳纳米片(NCF)和新型镍铁氧体-碳纳米片(NiFe@NCF)纳米复合材料。NCF来源于由Anabaena、Lyngbya和Weistiellopsis组成的蓝藻群,富含碳和氮。合成的纳米粒子被用作异相光催化剂,用于降解两种有害的水污染物:环丙沙星(CIP)和左氧氟沙星(LEV)。使用 NiFe@NCF 按照伪一阶动力学在可见光照射 50 和 70 分钟内降解了 99.91% 的 LEV 和 98.86% 的 CIP。纳米复合材料效率的提高可能是由于其表面积增大、带隙减小(从 2.42 eV 减小到 2.19 eV)、活性位点增多以及磁性镍纳米颗粒嵌入 NCF 后团聚趋势减弱导致电荷载流子迁移率增大。掺杂 N 提高了光收集特性,延缓了电荷重组,扩展并分散了ᴨ-共轭体系,从而增强了光催化活性。清除实验和 EPR 分析表明,和 -OH 是参与降解过程的主要活性物种。该材料在广泛的 pH 值范围内表现良好,可有效重复使用 5 次。此外,还提出了抗生素在 NiFe@NCF 纳米复合材料上的可行光催化降解机制,以及通过 LCMS 研究得出的可能降解途径。
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Photocatalytic degradation of antibiotics by N-doped carbon nanoflakes-nickel ferrite composite derived from algal biomass.

This work reports the synthesis of nickel ferrite (NiFe) nanoparticles, N-doped mesoporous carbon nanoflakes (NCF) and novel nickel ferrite-carbon nanoflakes (NiFe@NCF) nanocomposite using solvothermal method. NCF was derived from a cyanobacterial consortium consisting of Anabaena, Lyngbya and Weistiellopsis, rich in carbon and nitrogen. The synthesized nanoparticles were used as heterogeneous photocatalyst for degradation of two harmful water pollutants, ciprofloxacin (CIP) and levofloxacin (LEV). 99.91% LEV and 98.86% CIP were degraded within 50 and 70 min of visible light irradiation using NiFe@NCF following pseudo first order kinetics. This improved efficiency of the nanocomposite may be attributed to its higher surface area, reduction of band gap (from 2.42 to 2.19 eV), more active sites as well as charge carrier mobility with decreasing agglomeration tendency of the magnetic nickel nanoparticles upon being embedded on NCF. N-doping improves light harvesting property, retards charge recombination and extends as well as delocalises ᴨ-conjugated system resulting in enhanced photocatalytic activity. The scavenging experiments and EPR analysis reveal that O2-• and •OH are the main active species taking part in the degradation process. The material performs well within a wide range of pH and can be effectively used up to 5 repetitive cycles. A feasible photocatalytic degradation mechanism of the antibiotics against NiFe@NCF nanocomposite is also put forwarded along with their possible degradation pathways from LCMS studies.

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