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首页> 外文期刊>New Journal of Chemistry >Electron beam irradiation treatment of Ag/Bi2WO6/CdWO4 heterogeneous material with enhanced photocatalytic activity
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Electron beam irradiation treatment of Ag/Bi2WO6/CdWO4 heterogeneous material with enhanced photocatalytic activity

机译:具有增强的光催化活性Ag / Bi2wo6 / Cdwo4异质材料的电子束辐照处理

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摘要

An efficient ternary heterostructure material Ag/Bi2WO6/CdWO4 was prepared via a facile hydrothermal route. The in situ loading precisely regulated the distribution of silver nanoparticles on the heterojunction surface. Besides, electron beam irradiation was used for artificially creating interface defects in the material, so the specific surface area of the material was increased. The introduction of defects was conducive for the migration of catalytically active substances towards the surface of the material. Under visible light irradiation, the degradation efficiency of the heterostructure material was improved significantly. Within 20 min, the removal efficiency of the treated material for carmine could reach about 100% (50 mL, 50 mg L-1), while that for hexavalent chromium (Cr6+), it could reach about 100% (50 mL, 10 mg L-1) within 90 min. In addition, the results showed that 4% Ag load rate had the best improvement on the photocatalytic performance of the ternary heterostructure material, irrespective of the degradation process of carmine, Cr6+ or rhodamine B (RhB). Optimum amount of supported in situ nano-silver induced resonance of the plasma on the catalytic interface and synergized with Bi3+ to improve the catalytic efficiency. PL, DRS and XPS results proved that the ternary heterostructure could effectively inhibit the rapid recombination of electron hole pairs of Ag/Bi2WO6/CdWO4. As for the role of electron beam irradiation, it could improve the content of free hydroxyl groups on the material surface and enhance the catalytic capacity of the Ag/Bi2WO6/CdWO4 heterogeneous material. A feasible reaction pathway and photocatalytic mechanism for the degradation of carmine was investigated by gas chromatography-tandem mass spectrometry (GC-MS), and the main role of OH in the catalytic process was obtained by using different scavengers.
机译:通过容易的水热途径制备有效的三元异性结构材料AG / BI2WO6 / CDWO4。原位加载精确地调节了在异质结表面上的银纳米颗粒的分布。此外,电子束照射用于人工产生材料中的界面缺陷,因此材料的比表面积增加。缺陷引入有利于催化活性物质迁移到材料表面的迁移。在可见光照射下,异质结构材料的降解效率显着提高。在20分钟内,胭脂红的处理材料的去除效率可以达到约100%(50ml,50mg L-1),而对于六价铬(Cr6 +),它可以达到约100%(50ml,10mg L-1)90分钟内。此外,结果表明,4%Ag载荷率对三元异质结构材料的光催化性能具有最佳改善,而不管胭脂红,Cr6 +或罗丹明B(RHB)的降解过程。最佳量的原位纳米银诱导催化界面上等离子体的共振并用Bi3 +协同促进催化效率。 PL,DRS和XPS结果证明了三元异性结构可以有效地抑制AG / BI2WO6 / CDWO4的电子空穴对的快速重组。至于电子束照射的作用,它可以改善材料表面上游离羟基的含量,并增强Ag / Bi2wo6 / Cdwo4非均相材料的催化力。通过气相色谱 - 串联质谱(GC-MS)研究了可行的反应途径和用于降解胭脂红的光催化机制,通过使用不同的清除剂获得OH在催化过程中的主要作用。

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  • 来源
    《New Journal of Chemistry》 |2019年第35期|共11页
  • 作者单位

    Cent South Univ Forestry &

    Technol Coll Mat Sci &

    Engn Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Mat Sci &

    Engn Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Hubei Univ Sci &

    Technol Sch Nucl Technol &

    Chem &

    Biol Xianning 437100 Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

    Cent South Univ Forestry &

    Technol Coll Sci Changsha 410004 Hunan Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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