Ultraviolet–Visible Light–Sensitive High Surface Area Phosphorous-Fluorine–Co-Doped TiO2 Nanoparticles for the Degradation of Atrazine in Water

2014 ◽  
Vol 31 (7) ◽  
pp. 435-446 ◽  
Author(s):  
Javed Ali Khan ◽  
Changseok Han ◽  
Noor S. Shah ◽  
Hasan M. Khan ◽  
Mallikarjuna N. Nadagouda ◽  
...  
Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 872
Author(s):  
Nezar H. Khdary ◽  
Waleed S. Alkhuraiji ◽  
Tamil S. Sakthivel ◽  
Duaa N. Khdary ◽  
Mohamed Abdel Salam ◽  
...  

This work provides an alternate unique simple methodology to design and synthesize chemically modified nanophotocatalyst based on high surface area TiO2 nanoparticles that can be used efficiently for the photodegradation of organic pollutants under normal visible light rather than complicated UV irradiation. In this study, dual visible light and UV-driven nanophotocatalysts were synthesized via wet chemistry procedures using high surface area TiO2 nanoparticles functionalized with (3-Aminopropyl) trimethoxysilane and attached chemically to the CuXO to improve the charge separation and maintain the non-charge recombination. The successful modification of the TiO2 nanoparticles and the formation of the TiO2-NH2-CuxO nanophotocatalyst were confirmed using different characterization techniques, and the results revealed the synthesis of high surface area TiO2 nanoparticles, and their chemical modification with an amino group and further decoration with copper to produce TiO2-NH2-CuxO nanophotocatalyst. The photocatalytic activity of TiO2 and TiO2-NH2-CuxO nanophotocatalyst were evaluated using methylene blue (MB) dye; as an example of organic pollutants. The resulting TiO2-NH2-CuxO nanophotocatalyst exhibited superior photocatalytic activity for the degradation of MB dye under visible light irradiation, due to the reduction in the energy bandgap. The degradation of the MB dye using the TiO2-NH2-CuxO nanophotocatalyst was investigated using LC-MS, and the results revealed that the hydroxyl free radical is mainly responsible for the cleavage and the degradation of the MB dye.


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 235
Author(s):  
Hayette Benkhennouche-Bouchene ◽  
Julien G. Mahy ◽  
Cédric Wolfs ◽  
Bénédicte Vertruyen ◽  
Dirk Poelman ◽  
...  

TiO2 prepared by a green aqueous sol–gel peptization process is co-doped with nitrogen and zirconium to improve and extend its photoactivity to the visible region. Two nitrogen precursors are used: urea and triethylamine; zirconium (IV) tert-butoxide is added as a source of zirconia. The N/Ti molar ratio is fixed regardless of the chosen nitrogen precursor while the quantity of zirconia is set to 0.7, 1.4, 2, or 2.8 mol%. The performance and physico-chemical properties of these materials are compared with the commercial Evonik P25 photocatalyst. For all doped and co-doped samples, TiO2 nanoparticles of 4 to 8 nm of size are formed of anatase-brookite phases, with a specific surface area between 125 and 280 m2 g−1 vs. 50 m2 g−1 for the commercial P25 photocatalyst. X-ray photoelectron (XPS) measurements show that nitrogen is incorporated into the TiO2 materials through Ti-O-N bonds allowing light absorption in the visible region. The XPS spectra of the Zr-(co)doped powders show the presence of TiO2-ZrO2 mixed oxide materials. Under visible light, the best co-doped sample gives a degradation of p-nitrophenol (PNP) equal to 70% instead of 25% with pure TiO2 and 10% with P25 under the same conditions. Similarly, the photocatalytic activity improved under UV/visible reaching 95% with the best sample compared to 50% with pure TiO2. This study suggests that N/Zr co-doped TiO2 nanoparticles can be produced in a safe and energy-efficient way while being markedly more active than state-of-the-art photocatalytic materials under visible light.


2018 ◽  
Vol 2 (3) ◽  
pp. 25 ◽  
Author(s):  
Misaki Ota ◽  
Yuichiro Hirota ◽  
Yoshiaki Uchida ◽  
Norikazu Nishiyama

2018 ◽  
Vol 94 (4) ◽  
pp. 633-640 ◽  
Author(s):  
Bharath Velaga ◽  
Pradeep P. Shanbogh ◽  
Diptikanta Swain ◽  
Chandrabhas Narayana ◽  
Nalini G. Sundaram

RSC Advances ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 4763-4771 ◽  
Author(s):  
Muhammad Bilal Hussain ◽  
Malik Saddam Khan ◽  
Herman Maloko Loussala ◽  
Muhammad Sohail Bashir

Cr(vi) reduction is performed by BiOCl0.8Br0.2 composite produced via a facile in situ synthetic process at room temperature while making use of PVP (Mw = 10 000).


2019 ◽  
Vol 43 (48) ◽  
pp. 19372-19378 ◽  
Author(s):  
Jianyu Huang ◽  
Simin Liu ◽  
Zifang Peng ◽  
Zhuoxian Shao ◽  
Yuanyuan Zhang ◽  
...  

The synergistic effects of high surface area and abundant heteroatoms make porous carbons superior electrode materials.


Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 987 ◽  
Author(s):  
Hui Zhang ◽  
Qi Tang ◽  
Qingshan Li ◽  
Qingwen Song ◽  
Hailiang Wu ◽  
...  

In this study, the effects of disperse blue dye-sensitization on the photocatalytic properties of the Ag-N co-doped TiO2 nanoparticles loaded on polyethylene terephthalate (PET) filaments are investigated under visible light irradiation. The microstructure and photocatalytic properties of the as-synthesized TiO2 nanocomposites, as well as the as-prepared PET filaments, are systematically characterized. The photocatalytic performance of the PET filaments coated with the Ag-N co-doped TiO2 nanoparticles sensitized with disperse blue dyes is evaluated via its capacity of photo-degrading methyl orange (MO) dyes under visible light irradiation. It is found that the holes are the predominant reactive radical species and the hydroxyl and superoxide radicals play a subordinate role in the photocatalytic reaction process. The reaction rate constant of the photocatalytic composite filaments is nearly 4.0 times higher than that of the PET filaments loaded solely with TiO2 nanoparticles. The resultant photocatalytic composite filaments are evident to be capable of repeatedly photo-degrading MO dyes without losing its photocatalytic activity significantly.


2014 ◽  
Vol 69 (5) ◽  
Author(s):  
Ooi Yee Khai ◽  
Leny Yuliati ◽  
Siew Ling Lee

New visible light driven photocatalysts of 1 mol% Cr doped TiO2 supported on TUD-1 have been successfully synthesized. The Cr-TiO2/xTUD-1 (x = 10, 20, 30, 40 and 50) photocatalysts were prepared via surfactant-free sol-gel method followed by wet impregnation procedures. XRD analysis revealed that both TiO2 and Cr were incorporated in the highly porous siliceous matrix. FTIR analysis showed the existence of Si-O-Ti in all the materials. As observed, tetrahedral-coordinated Ti species were dominant in Cr-TiO2/10TUD-1, Cr-TiO2/20TUD-1 and Cr-TiO2/30TUD-1. Meanwhile, octahedral- coordinated Ti species were the dominant species in Cr-TiO2/40TUD-1 and Cr-TiO2/50TUD-1. It has been demonstrated that the amount of TUD-1 as photocatalyst support affected the wavelength response and the bandgap energy of the resulting materials. All the materials have bandgap energy of ~2.9 eV. The photocatalytic performance of the synthesized materials was tested out in dye photodegradation under visible light irradiation at 298 K for 5 hours. Results showed that all Cr-TiO2/TUD-1 materials had higher photocatalytic activity than that of Cr-TiO2. This could be explained by the high surface area and porosity provided by TUD-1 in enhancing the adsorption and diffusivities of the dye molecules, hence leading to the promising photocatalytic activity. Among the materials prepared, Cr-TiO2/30TUD-1 appeared as the most superior photocatalyst which gave the highest dye photodegradation.


RSC Advances ◽  
2019 ◽  
Vol 9 (42) ◽  
pp. 24368-24376 ◽  
Author(s):  
Ajay Kumar Adepu ◽  
Srinath Goskula ◽  
Suman Chirra ◽  
Suresh Siliveri ◽  
Sripal Reddy Gujjula ◽  
...  

In the present study, we synthesized several high-surface area V2O5/TiO2–SiO2 catalysts (vanado titanium silicate, VTS). The synthesized materials are characterized by PXRD, FE-SEM/EDAX, TEM, BET-surface area, FT-IR, UV-Vis, XPS, fluorescence and photocatalytic studies.


Sign in / Sign up

Export Citation Format

Share Document