scholarly journals Impact of TiO2 Nanotubes’ Morphology on the Photocatalytic Degradation of Simazine Pollutant

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2066 ◽  
Author(s):  
Syazwan Meriam Suhaimy ◽  
Chin Lai ◽  
Hairul Tajuddin ◽  
Emy Samsudin ◽  
Mohd Johan

There are various approaches to enhancing the catalytic properties of TiO2, including modifying its morphology by altering the surface reactivity and surface area of the catalyst. In this study, the primary aim is to enhance the photocatalytic activity by changing the TiO2 nanotubes’ architecture. The highly ordered infrastructure is favorable for a better charge carrier transfer. It is well known that anodization affects TiO2 nanotubes’ structure by increasing the anodization duration which in turn influence the photocatalytic activity. The characterizations were conducted by FE-SEM (fiend emission scanning electron microscopy), XRD (X-ray diffraction), RAMAN (Raman spectroscopy), EDX (Energy dispersive X-ray spectroscopy), UV-Vis (Ultraviolet visible spectroscopy) and LCMS/MS/MS (liquid chromatography mass spectroscopy). We found that the morphological structure is affected by the anodization duration according to FE-SEM. The photocatalytic degradation shows a photodegradation rate of k = 0.0104 min−1. It is also found that a mineralization of Simazine by our prepared TiO2 nanotubes leads to the formation of cyanuric acid. We propose three Simazine photodegradation pathways with several intermediates identified.

2014 ◽  
Vol 513-517 ◽  
pp. 33-36 ◽  
Author(s):  
Zi Chang Xie ◽  
Ying Wang ◽  
Peng Wang ◽  
Lei Zhang

In this paper, W-doped TiO2 (W-TiO2) powder was prepared in hydrothermal method by mixing TiO2 and ammonium metatungstate. The catalysts were characterized by X-ray diffraction and ultraviolet spectrophotometer. The results displayed that W-TiO2 showed an anatase crystallite structure with 2 % W content. W-element in W-TiO2 was amorphous state. The guaiacol was degraded with the W-TiO2 in the visible light. It was a model compounds of lignin existed in the plant fibers. The degradation rate of guaiacol was increased with the photocatalytic time, as high as 88.21 % after 360 min irradiation. It was concluded that the W-TiO2 had an obvious photocatalytic activity under visible light. It can be used in the photocatalytic degradation of lignin.


Author(s):  
Nurul Sahida Hassan ◽  
Nurul Jamilah Roslani ◽  
Aishah Abdul Jalil ◽  
Sugeng Triwahyono ◽  
Nur Fatien Salleh ◽  
...  

In recent years, dyes are one of the major sources of the water contamination that lead to environmental problems. For instance, Rhodamine B (RhB) which was extensively used as a colorant in textile industries is toxic and carcinogenic. Among many techniques, photocatalytic degradation become the promising one to remove those dyes from industrial wastewater. Recently, graphene has shown outstanding performance in this application due to its intrinsic electron delocalisation which promotes electron transport between composite photocatalyst and pollutant molecules. While, copper oxide (CuO) is well-known has a lower bandgap energies compared to other semiconductors. Therefore, in this study, copper oxide supported on graphene (CuO/G) was prepared and its photocatalytic activity was tested on degradation of RhB. The catalysts were characterized by X-Ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) Spectroscopy. The results showed that the interaction between copper and graphene support could enhance the photocatalytic activity. The 5 wt% CuO/G was found to give the highest degradation (95%) of 10 mg L-1 of RhB solution at pH 7 using 1 g L-1 catalyst after 4 hours under visible light irradiation. The photodegradation followed the pseudo first-order Langmuir-Hinshelwood kinetic model. This study demonstrated that the CuO/G has a potential to be used in photocatalytic degradation of various organic pollutants.


Author(s):  
Brijesh Pare ◽  
Satish Piplode ◽  
Vaishali Joshi

Flower like bismuth oxy chloride (BiOCl) was successfully synthesized by a simple hydrolytic method at room temperature. The precursor and as-prepared samples were characterized by X-ray diffraction (XRD), High Resolution Field Emission Scanning Electron Microscope (HR FESEM). The results indicated that the as-prepared BiOCl sample is self-assembled hierarchically with nano sheets. The photocatalytic activity of BiOCl was tested on the degradation of the Oxamyl (OM) under solar light irradiation. The results showed that pesticide molecules could be efficiently degraded over BiOCl under solar light irradiation. All the experiment were carried out in the following reaction condition, [OM] = 10-4 mol dm-3, BiOCl NPs= 40mg/50ml, pH= 6.3. Effect of operational parameter such as concentration of H2O2, K2S2O8, FeCl3, Fenton’s reagent (Fe3+/H2O2) and N2, O2 purging on the photocatalytic degradation was observed.


2019 ◽  
Vol 9 (8) ◽  
Author(s):  
Mohanna Zarei ◽  
Jamil Bahrami ◽  
Mohammad Zarei

Abstract Zirconia (ZrO2)-modified graphitic carbon nitride (g-C3N4) nanocomposite was used for effective photodegradation of 4-nitrophenol (4-NP) in water. The ZrO2 nanoparticles, g-C3N4 nanosheets, and ZrO2/g-C3N4 nanocomposite were well characterized by including N2 adsorption, X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, UV–Vis diffuse reflectance spectroscopy, photoelectrochemical measurements, and photoluminescence spectroscopy methods. ZrO2/g-C3N4 nanocomposites were formed at room temperature using sonication and used for effective for photodegradation of 4-NP under irradiation with visible light. The nanocomposite samples resulted in a significant increase in photocatalytic activity compared with single-component samples of g-C3N4. In particular, the ZrO2/g-C3N4 nanocomposite exhibited the significant increase in the photocatalytic activity. The ZrO2/g-C3N4 nanocomposite showed an excellent catalytic activity toward the reduction of 4-NP in aqueous medium. Further, ZrO2/g-C3N4 nanocomposite can be reused several times for photocatalytic degradation as well as for 4-NP adsorption.


2018 ◽  
Vol 54 (1A) ◽  
pp. 42
Author(s):  
Le Thi Ngoc Tu

The TiO2 nanotubes were fabricated by the hydrothermal method. Then, Ag nanoparticles with the varying ratio were attached on the TiO2 nanotubes by photoreduction. The characteristics of structure, morphology, chemical composition and of TiO2 nanotubes modified Ag (Ag-TNTs) was investigated by X-ray diffraction (XRD) and transmission electron microscopy (TEM), energy dispersive X-ray (EDX) and the absorption spectral of Methylene blue (MB) solution. The results showed that Ag-TNTs have fairly uniform length with Ag particles immobilized on the tube. The photocatalysis TiO2 nanotubes (TNTs) is higher than Ag-TNTs in UV range and lower than Ag-TNTs in the visible light. And the photocatalytic activity of Ag-TNTs with 5 wt.% Ag is highest in the visible range.


2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Mingjie Ma ◽  
Weijie Guo ◽  
Zhengpeng Yang ◽  
Shanxiu Huang ◽  
Guanyu Wang

TiO2/fine char (FC) photocatalyst was prepared via sol-gel method with tetrabutyl titanate as the precursor and FC as the carrier. The structural property of TiO2/FC photocatalyst was investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM), and the photocatalytic activity of TiO2/FC was evaluated by photocatalytic degradation of rhodamine B (RhB) aqueous solution under UV light irradiation. The results showed that TiO2was successfully coated on the surface of FC, and the TiO2/FC photocatalyst had better photocatalytic efficiency and stability for degradation of RhB under UV light illumination as compared to that of the pure TiO2and FC. The study provided a novel way for the application of FC to the photocatalytic degradation of organic wastes.


2011 ◽  
Vol 393-395 ◽  
pp. 1181-1184
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Qi Xing

Nd-doped Cu11O2 (VO4)6 photocatalyst was synthesized by complexing Sol-gel method and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and energy Dispersive X-Ray Spectroscopy(EDX). The photocatalytic activity of Nd-doped Cu11O2 (VO4)6 was evaluated by photocatalytic degradation of methyl orange (MO) solution under UV-light. It revealed that the Nd-doped Cu11O2 (VO4)6 prepared with the molar ratio of citric acid to metal inons be 2:1, Nd/Cu molar ratio of 2%, pH=7 and calcinated under 500°C for 4 hours was pure triclinic phase. In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 95.73% or so in 60min under 20W ultraviolet lamp.


2014 ◽  
Vol 807 ◽  
pp. 101-113 ◽  
Author(s):  
J. Theerthagiri ◽  
R.A. Senthil ◽  
J. Madhavan ◽  
B. Neppolian

The graphitic carbon nitride (g-C3N4) materials have been synthesized from nitrogen rich precursors such as urea and thiourea by directly heating at 520 °C for 2 h. The as-synthesized carbon nitride samples were characterized by x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-vis) absorption spectroscopy, photoluminescence (PL) and particle size analysis. The photoelectrochemical measurements were performed using several on-off cycles under visible-light irradiation. The x-ray diffraction peak is broader which indicates the fine powder nature of the synthesized materials. The estimated crystallite size of carbon nitrides synthesized from urea (U-CN) and thiourea (T-CN) are 4.0 and 4.4 nm respectively. The particle size of U-CN and T-CN were analysed by particle size analyser and were found to be 57.3 and 273.3 nm respectively. The photocatalytic activity for the degradation of the textile dye namely, direct red-81 (DR81) using these carbon nitrides were carried out under visible light irradiation. In the present investigation, a comparison study on the carbon nitrides synthesized from cheap precursors such as urea and thiourea for the degradation of DR81 has been carried out. The results inferred that U-CN exhibited higher photocatalytic activity than T-CN. The photoelectrochemical studies confirmed that the (e--h+) charge carrier separation is more efficient in U-CN than that of T-CN and therefore showed high photocatalytic degradation. Further, the smaller particle size of U-CN is also responsible for the observed degradation trend.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
R. M. Mohamed ◽  
M. A. Barakat

ZnO- nanoparticles were synthesized by a sol-gel technique from and tetraethyl orthosilicate (TEOS). The synthesized samples were further modified by nanosized Pt from H2PtCl6solution through photoassisted deposition (PAD) and impregnation (Img) routes. The obtained samples were characterized by a series of techniques including X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy, N2adsorption, extended X-ray absorption fine structure (EXAFS), and transmission electron microscopy (TEM). The photocatalytic activity of the Pt-ZnO/ was evaluated by photocatalytic degradation of phenol in synthetic wastewater under UV-irradiation. Results obtained revealed that the surface area and the photocatalytic activity of the prepared samples were increased in the order ZnO/ < PAD: Pt-ZnO/ < img: Pt-ZnO/. The surface area decreased from 480 to 460 and 450 m2/g, while the efficiency of the phenol degradation increased from 80 to 85 and 100%, with the ZnO/, Img: Pt-ZnO-, and PAD: Pt-ZnO- samples, respectively.


2017 ◽  
Vol 16 ◽  
pp. 63-66 ◽  
Author(s):  
Aurora Berlanga ◽  
Reyes Garcia-Diaz ◽  
Carlos Rodriguez Garcia ◽  
Jorge Oliva ◽  
Maria Teresa Romero ◽  
...  

Cooper doped SrAl2O4:xCu powders were synthesized by combustion method. The doping concentrations were x= 0.1%, 0.3%, 0.5%, and 1.0 at.%. X-ray diffraction patterns indicate that all Cu doped/undoped powders has monoclinic phase. Also, TEM images show that the size of the nanoparticles decreases as the content of Cu increases. The photocatalytic degradation of Congo red (CR) was studied by monitoring intensity of its characteristic absorbance band centered at 494 nm. The best result was obtained with the 0.1% Cu doped sample, since it degraded 100% of CR after 120 minutes under sunlight excitation. Hence, our results suggest that SrAl2O4:xCu powders could be suitable candidates for photocatalytic degradation of dye pollutants under sunlight.


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