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首页> 外文期刊>Chemosphere >Graphene modified anatase/titanate nanosheets with enhanced photocatalytic activity for efficient degradation of sulfamethazine under simulated solar light
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Graphene modified anatase/titanate nanosheets with enhanced photocatalytic activity for efficient degradation of sulfamethazine under simulated solar light

机译:具有增强的光催化活性的石墨烯改性的锐钛矿/钛酸酯纳米片,可在模拟太阳光下有效降解磺胺二甲嘧啶

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摘要

Graphene modified anatase/titanate nanosheets (G/A/TNS) synthesized through hydrothermal treatment were used for solar-light-driven photocatalytic degradation of a typical pharmaceutically active compound, sulfamethazine (SMT). The optimal material was synthesized with 0.5 wt% of graphene loading (G/A/TNS-0.5), which could efficiently degrade 96.1% of SMT at 4 h. G/A/TNS-0.5 showed enhanced photocatalytic activity compared with the neat anatase and unmodified anatase/titanate nanosheets (A/TNS). UV-vis diffuse reflection spectra indicated that G/A/TNS-0.5 had a lower energy band gap (E-g) of 2.8 eV than A/TNS (3.1 eV). The grafted graphene acted as an electron transfer mediator after photoexcitation, resulting in inhibition on rapid recombination of electron-hole pairs. More importantly, architecture of graphene and titanate nanosheets both with two-dimensional structures greatly facilitated the photoexcited electron transfer. center dot OH and O-1(2) were the primary reactive oxygen species (ROS) to SMT degradation. Fukui index (f(-)) derived from density functional theory (DFT) calculation predicted the active sites on SMT molecule, and then SMT degradation pathway was proposed by means of intermediates identification and theoretical calculation. Furthermore, G/A/TNS-0.5 could be well reused and 90.5% of SMT was also degraded after five runs. The developed new photocatalysts show great potential for degradation of emerging organic contaminants through photocatalysis under solar light. (C) 2019 Elsevier Ltd. All rights reserved.
机译:通过水热处理合成的石墨烯修饰的锐钛矿/钛酸酯纳米片(G / A / TNS)用于太阳光驱动的典型药物活性化合物磺胺二甲嘧啶(SMT)的光催化降解。合成的最佳材料的石墨烯负载量为0.5 wt%(G / A / TNS-0.5),可在4 h时有效降解96.1%的SMT。与纯锐钛矿和未修饰的锐钛矿/钛酸酯纳米片(A / TNS)相比,G / A / TNS-0.5显示出增强的光催化活性。紫外可见漫反射光谱表明,G / A / TNS-0.5的能带隙(E-g)比A / TNS(3.1 eV)低,为2.8 eV。接枝的石墨烯在光激发后充当电子转移介质,导致抑制电子-空穴对的快速重组。更重要的是,具有二维结构的石墨烯和钛酸酯纳米片的结构极大地促进了光激发电子的转移。中心点OH和O-1(2)是SMT降解的主要活性氧(ROS)。通过密度泛函理论(DFT)计算得出的Fukui指数(f(-))预测了SMT分子上的活性位点,然后通过中间体鉴定和理论计算,提出了SMT降解途径。此外,G / A / TNS-0.5可以很好地重复使用,并且经过5次运行后SMT的90.5%也会降解。已开发的新型光催化剂显示出在太阳光下通过光催化降解新兴有机污染物的巨大潜力。 (C)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere》 |2019年第10期|198-206|共9页
  • 作者单位

    Taiyuan Univ Sci & Technol, Inst Environm Sci, Taiyuan 030024, Shanxi, Peoples R China;

    Peking Univ, Coll Environm Sci & Engn, Key Lab Water & Sediment Sci, Minist Educ, Beijing 100871, Peoples R China;

    Peking Univ, Coll Environm Sci & Engn, Key Lab Water & Sediment Sci, Minist Educ, Beijing 100871, Peoples R China;

    Peking Univ, Coll Environm Sci & Engn, Key Lab Water & Sediment Sci, Minist Educ, Beijing 100871, Peoples R China|Peking Univ, BIC ESAT, Beijing 100871, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Graphene; Titanium nanomaterials; Pharmaceuticals; Photocatalysis; DFT calculation;

    机译:石墨烯钛纳米材料药物光催化DFT计算;

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