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Photocatalytic activity of synthesized titanate nanotubes and nanoribbons vs. commercial TiO_2 under artificial solar and visible irradiation using 17β-estradiol as model micropollutant

机译:17β-雌二醇为模型微污染物在人工太阳光和可见光下合成钛酸酯纳米管和纳米带对商用TiO_2的光催化活性

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The aim of this study was to compare photocatalytic activity of protonated titanate nanotubes (HTiNT) and nanoribbons (HTiNR) vs. TiO2 P25 under different irradiation conditions for degradation of selected water micropollutant (17 beta-estradiol, E2). HTiNT and HTiNR were prepared according to previously published method, hereby confirmed by means of the scanning electron microscopy and powder X-ray diffraction (XRD). In order to check the extent of photocatalytic activity at high E2 photolysis rates due to its absorption maximum (lambda(max) = 278 nm), reaction cell was exposed to the source of artificial solar light with enhanced UVB irradiation. HTiNT, HTiNR and commercial TiO2 were active under both visible light and solar irradiation. In each irradiation regime, the E2 degradation followed pseudo-first-order kinetics with respect to both irradiation time and energy. The rate constant decreased with the decreasing catalyst load while increased with the increasing irradiation energy for the emissions below 400 nm. On behalf of achieved nanostructural arrays the wider bandgaps were shown for HTiNT and HTiNR. Compared with TiO2 P25 almost three times lower rate constants for E2 degradation under visible irradiation were observed on behalf of band alignment effect of the P25. The photonic efficiencies (zeta(0)) were calculated and used for quantitative comparison of HTiNT, HTiNR and TiO2 photocatalytic activity regardless the irradiation conditions. The respective values decreased with the higher irradiation energy as related to an excess of photons available for simultaneous photolysis of E2 and its degradation intermediates.
机译:这项研究的目的是比较质子化的钛酸酯纳米管(HTiNT)和纳米带(HTiNR)与TiO2 P25在不同照射条件下对所选水微污染物(17β-雌二醇,E2)的降解的光催化活性。根据先前公开的方法制备HTnNT和HTinR,据此通过扫描电子显微镜和粉末X射线衍射(XRD)证实。为了检查由于其最大吸收(λ(max)= 278 nm)而在高E2光解速率下的光催化活性程度,将反应池暴露于具有增强UVB辐射的人造太阳光源中。 HTiNT,HTiNR和市售TiO2在可见光和太阳辐射下均具有活性。在每种照射方式下,E2降解均遵循关于照射时间和能量的伪一级动力学。对于低于400 nm的发射,速率常数随着催化剂负载的减少而降低,而随着辐照能量的增加而增加。代表已实现的纳米结构阵列,显示了针对HTiNT和HTiNR的更宽的带隙。与TiO2 P25相比,观察到代表P25的能带排列效应,可见光下E2降解的速率常数几乎降低了三倍。计算光子效率(zeta(0)),并用于定量比较HTiNT,HTnNR和TiO2光催化活性,而与照射条件无关。相应的值随着较高的照射能量而降低,这与可用于E2及其降解中间体的同时光解的过量光子有关。

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