scholarly journals Visible light photocatalytic activity of TiO2 deposited on activated carbon

2013 ◽  
Vol 11 (3) ◽  
pp. 464-470 ◽  
Author(s):  
Alexander Eliyas ◽  
Ljutzkan Ljutzkanov ◽  
Irina Stambolova ◽  
Vladimir Blaskov ◽  
Sasho Vassilev ◽  
...  

AbstractAbstract Four photocatalyst samples, prepared from beech sawdust, were synthesized by an original method, combining pyrolysis and impregnation — two of them: TiO2 + activated carbon and other two — only activated carbon. The pyrolysis process has been carried out at two different temperatures — 680°C and 830°C. The prepared samples were characterized by a series of methods — XRD, BET, SEM and DTA/TG. The most important result was achieving visible light photocatalytic activity with an azo dye pollutant for both materials. The TiO2/AC-680°C sample demonstrated higher activity under visible light illumination than the TiO2/AC-830°C sample. The visible light activity was attributed to the active carbon component in the composite materials, which was evidenced by the photocatalytic tests with bare carbon (without any TiO2) manifesting visible light activity. The AC-680°C carbon was superior to the AC-830°C under visible illumination probably due to its higher specific surface area and porous texture. UV-light testing of the photocatalytic activity revealed that the TiO2/AC-680°C sample was higher than that of the TiO2/AC-830°C under polychromatic UV-A illumination (320–400 nm with a maximum at l = 365 nm). The TiO2/AC-680°C sample was also more efficient with the monochromatic UV-C illumination (l = 254 nm). Graphical abstract

2009 ◽  
Vol 16 (04) ◽  
pp. 563-567 ◽  
Author(s):  
JIWEI ZHANG ◽  
JINGWEI ZHANG ◽  
ZHENSHENG JIN ◽  
ZHISHEN WU ◽  
ZHIJUN ZHANG

TiO 2 samples with different crystal forms were treated in flowing NH 3 at elevated temperatures to fabricate N -doped TiO 2 photocatalysts with different crystal forms. The resulting N -doped TiO 2 photocatalysts were characterized by means of X-ray diffraction, transmission electron microscopy, diffusion reflectance spectrometry, and X-ray photoelectron spectroscopy. The visible-light photocatalytic activity of the catalysts was evaluated by measuring the photocatalyzed removal rate of propylene. Results indicate that the visible-light activity of N -doped TiO 2 photocatalysts is highly dependent on the crystal form. Namely, N -doped anatase TiO 2 has the highest visible-light activity, while the visible-light activity of N -doped TiO 2 photocatalysts decreases with decreasing content of anatase phase and increasing content of rutile phase. In addition N -doped rutile TiO 2 has no visible-light photocatalytic activity.


2014 ◽  
Vol 43 (39) ◽  
pp. 14537-14541 ◽  
Author(s):  
Yong Qiu ◽  
Xinjun Li

Peroxo-titanium decorated H-titanate-nanotube-based hierarchical microspheres were prepared by a hydrothermal method, and they exhibited enhanced visible-light activity.


2016 ◽  
Vol 705 ◽  
pp. 385-389 ◽  
Author(s):  
Dustin Loren V. Almanza ◽  
Maria Carmela T. Garcia ◽  
Alenn D. Prodigalidad ◽  
Marvin U. Herrera

Many traditional photocatalytic materials such as ZnO and TiO2 are ultraviolet light-triggered due to their wide band gap, however indoor light and sunlight reaching the surface of the earth are in the visible light region. This research aims to fabricate a photocatalytic material that can be triggered using visible light. Ceramic composites with ZnO and CuO interfaces were constructed using heterogeneous mixing technique. The photocatalytic activities of the samples were determined through their ability to degrade methyl orange dye under visible light illumination. Results show that the existence of the ZnO-CuO interface improved the visible light photocatalytic activity of the material.


Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3948
Author(s):  
Lingfang Qiu ◽  
Zhiwei Zhou ◽  
Mengfan Ma ◽  
Ping Li ◽  
Jinyong Lu ◽  
...  

Novel visible-light responded aluminosilicophosphate-5 (SAPO-5)/g-C3N4 composite has been easily constructed by thermal polymerization for the mixture of SAPO-5, NH4Cl, and dicyandiamide. The photocatalytic activity of SAPO-5/g-C3N4 is evaluated by degrading RhB (30 mg/L) under visible light illumination (λ > 420 nm). The effects of SAPO-5 incorporation proportion and initial RhB concentration on the photocatalytic performance have been discussed in detail. The optimized SAPO-5/g-C3N4 composite shows promising degradation efficiency which is 40.6% higher than that of pure g-C3N4. The degradation rate improves from 0.007 min−1 to 0.022 min−1, which is a comparable photocatalytic performance compared with other g-C3N4-based heterojunctions for dye degradation. The migration of photo-induced electrons from g-C3N4 to the Al site of SAPO-5 should promote the photo-induced electron-hole pairs separation rate of g-C3N4 efficiently. Furthermore, the redox reactions for RhB degradation occur on the photo-induced holes in the g-C3N4 and Al sites in SAPO-5, respectively. This achievement not only improves the photocatalytic activity of g-C3N4 efficiently, but also broadens the application of SAPOs in the photocatalytic field.


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