埃洛石
光降解
降级(电信)
催化作用
材料科学
三乙醇胺
化学工程
激进的
吸附
比表面积
光催化
煅烧
石墨氮化碳
罗丹明B
光化学
无机化学
化学
复合材料
有机化学
分析化学(期刊)
工程类
电信
计算机科学
作者
L. Santamaría,S.A. Korili,A. Gil,José M. López‐de‐Luzuriaga,Miguel Monge
出处
期刊:Catalysis Today
[Elsevier]
日期:2024-02-16
卷期号:432: 114584-114584
被引量:4
标识
DOI:10.1016/j.cattod.2024.114584
摘要
Silica nanotubes, obtained from halloysite clay nanotubes that were calcined and acid-activated, were used as support for graphitic carbon nitride (g-C3N4) via a simple deposition method. They were chosen in order to avoid any agglomeration issues, as there was an increase of the specific surface area with respect to pristine halloysite. The composite was tested for the degradation of a persistent emerging pollutant in water, namely, antibiotic norfloxacin. Experiments were performed in darkness (until adsorption-desorption equilibrium was attained) and, subsequently under visible light. Comparison of the performance between the photocatalysts shows that the composite was 49% faster than g-C3N4. The introduction of persulfate in the lumen of the nanotubes via vacuum negative-pressure suction and injection was also tested for the generation of ⋅OH radicals that fasten the degradation rate, obtaining a further 47% increase in the degradation rate of norfloxacin thanks to the release of this anion during the photodegradation process. The degradation mechanism of SiO2/g-C3N4 sample was studied with trapping experiments by the use of scavengers that were introduced to quench the photodegradation: triethanolamine for photoexcited holes (h+), tert-butanol for hydroxyl radicals (⋅OH) and a N2 atmosphere for superoxide radicals (⋅O2).
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