scholarly journals Visible Light Induced Photocatalytic Degradation of Methyl Red with Codoped Titania

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Susmitha Thota ◽  
Siva Rao Tirukkovalluri ◽  
Sreedhar Bojja

Photocatalysis using semiconductor oxides was being investigated extensively for the degradation of dyes in effluent water. This paper reports our findings on visible light induced photocatalytic degradation of azo dye, methyl red mediated nitrogen and manganese codoped nano-titanium dioxide (N/Mn-TiO2). The codoped samples with varying weight percentages were synthesized by sol-gel method and characterized by various analytical techniques. The X-ray diffraction data showed that the synthesized samples were in anatase phase with 2θ at 25.3°. UV-visible diffuse reflectance spectral analysis revealed that the presence of dopants in TiO2 caused a significant absorption shift towards visible region and their presence was confirmed by X-ray photoelectron spectral data. The release of hydroxyl radical (major active species in photocatalytic degradation) by the photocatalyst in aqueous solution under visible light irradiation was quantitatively investigated by the photoluminiscent technique (PL). The effect of various experimental parameters like dopant concentration, pH, catalyst dosage, and initial dye concentrations was investigated and optimum conditions were established. The extent of mineralization of methyl red was studied by chemical oxygen demand (COD) assays and the results showed complete mineralization of the dye.

2018 ◽  
Vol 55 (4C) ◽  
pp. 277 ◽  
Author(s):  
Nguyen Thi Phuong Mai

In the present paper, photocatalytic degradation of paraquat using N-TiO2/SiO2 with different molar ratio of titanium: nitrogen (Ti:N) under visible light was investigated. The catalyst was prepared via immersed SiO2 in N-TiO2. N-TiO2 was synthesized by sol-gel method.  The N-TiO2/SiO2 catalyst was characterized using X-ray diffraction, UV diffuse reflectance spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy. The results from characterizations indicated that N-doped anatase TiO2 had a 20-25 nm size. Degradation of paraquat, at an initial concentration of 10 mg/L was determined by UV-Vis. Chemical oxygen demand (COD) was used for process performance. Based on the COD tests, the COD values in residual paraquat was lower than that in initial paraquat concentration after 8 hours illumination of visible light. Moreover, the experiment’s results indicated that 80% of paraquat was degraded within 8 h of illumination time. These results showed that N-TiO2/SiO2 with molar Ti:N=2:1 gives the highest degradation efficiency of paraquat under visible light. This catalyst was stable and reusable suggesting it can be applied to treat organic pollutant in water. 


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
T. Siva Rao ◽  
Teshome Abdo Segne ◽  
T. Susmitha ◽  
A. Balaram Kiran ◽  
C. Subrahmanyam

Photocatalytic activity of TiO2was studied by doping with magnesium (Mg2+-TiO2) with varying magnesium weight percentages ranging from 0.75–1.5 wt%. The doped and undoped samples were synthesized by sol-gel method and characterized by X-ray diffraction (XRD), N2adsorption-desorption (BET), X-ray photoelectron spectroscopy (XPS), UV-visible diffuse reflectance spectroscopy (DRS), and scanning electron microscopy (SEM). The XRD data has shown that anatase crystalline phase in Mg2+-TiO2catalysts, indicating that Mg2+ions did not influence the crystal patterns of TiO2. The presence of magnesium ions in TiO2matrix has been determined by XPS spectra. DRS spectra showed that there is a significant absorption shift towards the visible region for doped TiO2. The SEM images and BET results showed that doped catalyst has smaller particle size and highest surface area than undoped TiO2. The photocatalytic efficiency of the synthesized catalysts was investigated by the photocatalytic degradation of aqueous dichlorvos (DDVP) under visible light irradiation, and it was found that the Mg2+-doped catalysts have better catalytic activity than undoped TiO2. This can be attributed that there is a more efficient electron-hole creation in Mg2+-TiO2in visible light, contrary to undoped TiO2which can be excited only in UV irradiation. The effect of dopant concentration, pH of solution, dosage of catalysts, and initial pesticide concentration has been studied.


Author(s):  
Snehamol Mathew ◽  
Priyanka Ganguly ◽  
Stephen Rhatigan ◽  
Vignesh Kumaravel ◽  
Ciara Byrne ◽  
...  

Indoor surface contamination by microbes is a major public health concern. A damp environment is one potential sources for microbe proliferation. Smart photocatalytic coatings on building surfaces using semiconductors like titania (TiO<sub>2</sub>) can effectively curb this growing threat.<b> </b>Metal-doped titania in anatase phase has been proved as a promising candidate for energy and environmental applications. In this present work, the antimicrobial efficacy of copper (Cu) doped TiO<sub>2 </sub>(Cu-TiO<sub>2</sub>) was evaluated against <i>Escherichia coli</i> (Gram-negative) and <i>Staphylococcus aureus</i> (Gram-positive) under visible light irradiation. Doping of a minute fraction of Cu (0.5 mol %) in TiO<sub>2 </sub>was carried out <i>via</i> sol-gel technique. Cu-TiO<sub>2</sub> further calcined at various temperatures (in the range of 500 °C – 700 °C) to evaluate the thermal stability of TiO<sub>2</sub> anatase phase. The physico-chemical properties of the samples were characterised through X-ray diffraction (XRD), Raman spectroscopy, X-ray photo-electron spectroscopy (XPS) and UV-visible spectroscopy techniques. XRD results revealed that the anatase phase of TiO<sub>2</sub> was maintained well, up to 650 °C, by the Cu dopant. UV-DRS results suggested that the visible light absorption property of Cu-TiO<sub>2 </sub>was enhanced and the band gap is reduced to 2.8 eV. Density functional theory (DFT) studies emphasises the introduction of Cu<sup>+</sup> and Cu<sup>2+</sup> ions by replacing Ti<sup>4+</sup> ions in the TiO<sub>2</sub> lattice, creating oxygen vacancies. These further promoted the photocatalytic efficiency. A significantly high bacterial inactivation (99.9%) was attained in 30 mins of visible light irradiation by Cu-TiO<sub>2</sub>.


2010 ◽  
Vol 8 (1) ◽  
pp. 142-148 ◽  
Author(s):  
L. Gomathi Devi ◽  
Nagaraju Kottam ◽  
S. Girish Kumar ◽  
K. Eraiah Rajashekhar

AbstractAnatase TiO2 was prepared by sol-gel method through the hydrolysis of TiCl4. Ni2+ was doped into the TiO2 matrix in the concentration range of 0.02 to 0.1 at.% and characterized by various analytical techniques. Powder X-ray diffraction revealed only anatase phase for all the samples, while diffuse reflectance spectral studies indicated a red shift in the band gap absorption to the visible region. The photocatalytic activities of these photocatalysts were probed for the degradation of methyl orange under natural solar light. The photocatalyst with optimum doping of 0.08 at.% Ni2+, showed enhanced activity, which is attributed to: (i) effective separation of charge carriers and (ii) large red shift in the band gap to visible region. The influence of crystallite size and dopant concentration on the charge carrier trapping — recombination dynamics is investigated.


2012 ◽  
Vol 712 ◽  
pp. 73-83 ◽  
Author(s):  
C. Karunakaran ◽  
P. Magesan ◽  
P. Gomathisankar

Bi2O3-TiO2 nanocomposites were obtained by sol-gel method using tween 80 (T-80) or polyvinyl pyrrolidone-polyethylene glycol (PVP-PEG) as templating agent. The powder X-ray diffraction (XRD) patterns of both the composites reveal the crystal structure of Bi2O3 as primitive tetragonal and TiO2 is in anatase phase. The energy dispersive X-ray (EDX) spectra provide the composition of Bi2O3 in Bi2O3-TiO2 (T-80) and Bi2O3-TiO2 (PVP-PEG) as 3.8 and 20.4 mol. %, respectively. The average crystallite sizes of Bi2O3-TiO2 (T-80) and Bi2O3-TiO2 (PVP-PEG), derived from XRD, are 9 and 17 nm, respectively. The scanning electron microscopic (SEM) images show the spherical shape of Bi2O3-TiO2 (T-80) and the composites are polycrystalline. The diffuse reflectance spectra (DRS) of the composites display faint absorption of visible light and strong absorption in UV-A region. The photoluminescence (PL) spectra of both the composites are similar and the observed near band gap emission (NBE) and deep level emission (DLE) agree with those of TiO2. The impedance spectra show that the charge-transfer resistances of the composites do not differ significantly. The visible light photoimpedance spectra display the photoconductance of Bi2O3-TiO2 (PVP-PEG) but not that of Bi2O3-TiO2 (T-80). Although the visible light-photocatalytic activities of the two nanocomposites to degrade dye do not differ significantly Bi2O3-TiO2 (T-80) under UV-A light degrades dyes faster than Bi2O3-TiO2 (PVP-PEG).


2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Xiuwen Cheng ◽  
Xiujuan Yu ◽  
Zipeng Xing ◽  
Lisha Yang

Anatase mesoporous titanium dioxide codoped with nitrogen and chlorine (N-Cl-TiO2) photocatalysts were synthesized through simple one-step sol-gel reactions in the presence of ammonium chloride. The resulting materials were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible diffuse reflection spectrum (UV-vis DRS). XRD results indicated that codoping with nitrogen and chlorine could effectively retard the phase transformation of TiO2from anatase to rutile and the growth of the crystallite sizes. XPS revealed that nitrogen and chlorine elements were incorporated into the lattice of TiO2through substituting the lattice oxygen atoms. DRS exhibited that the light absorption of N-Cl-TiO2in visible region was greatly improved. As a result, the band gap of TiO2was reduced to 2.12 eV. The photocatalytic activity of the as-synthesized TiO2was evaluated for the degradation of RhB and phenol under visible light irradiation. It was found that N-Cl-TiO2catalyst exhibited higher visible light photocatalytic activity than that of P25 TiO2and N-TiO2, which was attributed to the small crystallite size, intense light absorption in visible region, and narrow band gap.


2018 ◽  
Vol 15 (3) ◽  
pp. 197-208 ◽  
Author(s):  
Ravi Kamble ◽  
Smita Mahajan ◽  
Vijaya Puri ◽  
Harish Shinde ◽  
Kalayanrao Garadkar

TiO2 and Cu-doped TiO2 nanoparticles (NPs) with totally extraordinary substance of Cu by exploitation hydrothermal method. The part immaculateness, morphology, molecule estimate, optical properties, and elemental composition of as-incorporated Cu-doped TiO2 NPs were investigated by numerous systematic methods. The XRD designs unveiled Cu-doped TiO2 NPs inside the part unadulterated anatase phase. The plane of (101) XRD and XPS results show the lucky doping of Cu2+ inside the TiO2 lattice. The optical edges of Cu-doped TiO2 demonstrated a transparent light absorption in visible region that assumes an essential part inside the photocatalytic action underneath characteristic daylight. Certain Cu2+ content shows least PL intensity that backings the decrease in recombination rate of charge species. In addition, to get a handle on photocatalytic action, we have tried Cu-doped TiO2 for the degradation of Malachite Green (MG) under visible light. A large portion of 85% degradation was found for Cu-doped TiO2 (1.71 wt.%) underneath daylight minimum of 180 min, severally, that is past that of TiO2 (53%). Also, the degradation of the MG was affirmed by measurement of the chemical oxygen demand of the photodegraded solution. These outcomes demonstrates that the Cu-doped TiO2 NPs are extremely productive for the photodegration of the MG.


2016 ◽  
Vol 69 (6) ◽  
pp. 638 ◽  
Author(s):  
Shoutai Wei ◽  
Hualong Liu ◽  
Chiyang He ◽  
Ying Liang

In this paper, a molecularly imprinted TiO2/WO3-coated magnetic Fe3O4@SiO2 nanocomposite was developed for photocatalytic degradation. Fe3O4 nanoparticles were first prepared by a traditional co-precipitation method, and then a SiO2 shell was grown on the surface of the Fe3O4 nanoparticles. Finally, a 4-nitrophenol imprinted TiO2/WO3 coating was obtained on the surface of the Fe3O4@SiO2 nanocomposite via a sol-gel method and subsequent calcination. The new composite was characterised by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), high resolution TEM (HRTEM) and vibrating sample magnetometry (VSM). In addition, the adsorption ability and photocatalytic activity of the composite were investigated. Results showed that the imprinted composite had higher adsorption ability for the template than the non-imprinted composite. The imprinted catalyst could degrade 4-nitrophenol under visible light with a first-order reaction rate of 0.1039 h–1, which was ~2.5 times that of the non-imprinted catalyst. The new imprinted catalyst showed good catalytic selectivity, an ease of being recycled by an external magnetic field, good reusability, no need for additional chemicals, and allows the possibility of utilising solar light as energy resource. Therefore, the catalyst can be potentially applied for ‘green’, low-cost and effective degradation of 4-nitrophenol in real wastewater.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Eric S. Agorku ◽  
Bhekie B. Mamba ◽  
Avinash C. Pandey ◽  
Ajay K. Mishra

A series of S/Gd3+-codoped TiO2photocatalysts were synthesized by a modified sol-gel method. The materials were characterized by X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), UV-visible diffuse reflectance spectroscopy, scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM)/energy-dispersive spectroscopy (EDS). Laboratory experiments with Indigo Carmine chosen as a model for organic pollutants were used to evaluate the photocatalytic performance of S/Gd3+-codoped TiO2under visible-light with varying concentrations of Gd3+ions in the host material. XRD and Raman results confirmed the existence of anatase phase TiO2with particle size ranging from 5 to 12 nm. Codoping has exerted a great influence on the optical responses along with red shift in the absorption edge. S/Gd3+-codoped TiO2showed significant visible-light induced photocatalytic activity towards Indigo Carmine dye compared with S-TiO2or commercial TiO2. TiO2-S/Gd3+(0.6% Gd3+) degraded the dye (ka= 5.6 × 10−2 min−1) completely in 50 min.


2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Douga Nassoko ◽  
Yan-Fang Li ◽  
Jia-Lin Li ◽  
Xi Li ◽  
Ying Yu

Titanium dioxide (TiO2) doped with neodymium (Nd), one rare earth element, has been synthesized by a sol-gel method for the photocatalytic degradation of rhodamine-B under visible light. The prepared samples are characterized by X-ray diffractometer, Raman spectroscopy, UV-Vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller measurement. The results indicate that the prepared samples have anatase and brookite phases. Additionally, Nd as Nd3+may enter into the lattice ofTiO2and the presence of Nd3+substantially enhances the photocatalytic activity ofTiO2under visible light. In order to further explore the mechanism of photocatalytic degradation of organic pollutant, photoluminescence spectrometer and scavenger addition method have been employed. It is found that hydroxide radicals produced by Nd-dopedTiO2under visible light are one of reactive species for Rh-B degradation and photogenerated electrons are mainly responsible for the formation of the reactive species.


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