An efficient eco advanced oxidation process for phenol mineralization using a 2D/3D nanocomposite photocatalyst and visible light irradiations
Author | Al-Kandari, H. |
Author | Abdullah, A. M. |
Author | Ahmad, Yahia H. |
Author | Al-Kandari, S. |
Author | Alqaradawi, Siham Y. |
Author | Mohamed, A.M. |
Available date | 2020-09-03T08:58:10Z |
Publication Date | 2017 |
Publication Name | Scientific Reports |
Resource | Scopus |
ISSN | 20452322 |
Abstract | Nanocomposites (CNTi) with different mass ratios of carbon nitride (C3N4) and TiO2 nanoparticles were prepared hydrothermally. Different characterization techniques were used including X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), transmission electron spectroscopy (TEM) and Brunauer-Emmett-Teller (BET). UV-Vis DRS demonstrated that the CNTi nanocomposites exhibited absorption in the visible light range. A sun light-simulated photoexcitation source was used to study the kinetics of phenol degradation and its intermediates in presence of the as-prepared nanocomposite photocatalysts. These results were compared with studies when TiO2 nanoparticles were used in the presence and absence of H2O2 and/or O3. The photodegradation of phenol was evaluated spectrophotometrically and using the total organic carbon (TOC) measurements. It was observed that the photocatalytic activity of the CNTi nanocomposites was significantly higher than that of TiO2 nanoparticles. Additionally, spectrophotometry and TOC analyses confirmed that degraded phenol was completely mineralized to CO2 and H2O with the use of CNTi nanocomposites, which was not the case for TiO2 where several intermediates were formed. Furthermore, when H2O2 and O3 were simultaneously present, the 0.1% g-C3N4/TiO2 nanocomposite showed the highest phenol degradation rate and the degradation percentage was greater than 91.4% within 30 min. 1 2017 The Author(s). |
Language | en |
Publisher | Nature Publishing Group |
Subject | Cyanogen Heptazine Photocatalysts |
Type | Article |
Issue Number | 1 |
Volume Number | 7 |
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