scholarly journals Effect of Isopropanol on Microstructure and Activity of TiO2Films with Dominant {001} Facets for Photocatalytic Degradation of Bezafibrate

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Murtaza Sayed ◽  
Fu Pingfeng ◽  
Hasan M. Khan ◽  
Pengyi Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Hydroxyl Radicals ◽  
Terephthalic Acid ◽  
Hydrothermal Solution ◽  
Titanium Sheet ◽  
Fluoride Ions ◽  
Chromatography Tandem Mass Spectrometry ◽  
Liquid Chromatography Tandem Mass ◽  
Degradation Intermediates

Titanium dioxide (TiO2) films with dominant {001} facets coated on a titanium sheet (Ti) were synthesized with the simple hydrothermal method by using Ti as the precursor and substrate. The effect of addition of isopropanol into the hydrothermal solution on the structure, photocatalytic activity, and stability of as-synthesized TiO2films was investigated. The presence of isopropanol obviously influenced the microstructure of as-synthesized TiO2films, which was converted from microspheres into irregular close stack of truncated tetrahedrons. And the percentage of exposed {001} facets calculated from the Raman spectra increased from 48.2% to 57%. Accordingly, the TiO2films prepared with addition of isopropanol showed high and stable photocatalytic activity, which is nearly 2.6 times as that of the conventional P25 TiO2coated on Ti-substrate. In addition, the photocatalytic activity of as-synthesized TiO2films was greatly enhanced after calcination treatment at 600°C, which can be attributed to removal of fluoride ions and organic residuals adsorbed on the surface of the catalyst. Photoluminescence (PL) technique was used for the detection of produced hydroxyl radicals (•OH) on the surface of UV-illuminated TiO2using terephthalic acid as probe molecule. The photocatalytic degradation intermediates of bezafibrate were analyzed by an ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), and accordingly the degradation pathways were proposed.

scholarly journals Effective Photocatalytic Activity of Sulfate-Modified BiVO4 for the Decomposition of Methylene Blue Under LED Visible Light

Materials ◽  
2019 ◽  
Vol 12 (17) ◽  
pp. 2681 ◽  
Author(s):  
Vinh Huu Nguyen ◽  
Quynh Thi Phuong Bui ◽  
Dai-Viet N. Vo ◽  
Kwon Taek Lim ◽  
Long Giang Bach ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Hydroxyl Radicals ◽  
High Efficiency ◽  
Separation Efficiency ◽  
Diffuse Reflectance Spectroscopy ◽  
Removal Rate ◽  
Gravimetric Analysis ◽  
X Ray

In this study, we investigated sulfate-modified BiVO4 with the high photocatalytic activity synthesized by a sol-gel method in the presence of thiourea, followed by the annealing process at different temperatures. Its structure was characterized by thermal gravimetric analysis (TGA), powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS). The BiVO4 synthesized in the presence of thiourea and calcined at 600 °C (T-BVO-600) exhibited the highest photocatalytic degradation efficiency of methylene blue (MB) in water; 98.53% MB removal was achieved within 240 min. The reaction mechanisms that affect MB photocatalytic degradation on the T-BVO-600 were investigated via an indirect chemical probe method, using chemical agents to capture the active species produced during the early stages of photocatalysis, including 1,4-benzoquinone (scavenger for O2−), ethylenediaminetetraacetic acid disodium salt (scavenger for h+), and tert-butanol (scavenger for HO•). The results show that holes (h+) and hydroxyl radicals (HO•) are the dominant species of MB decomposition. Photoluminescence (PL) measurement results of terephthalic acid solutions in the presence of BiVO4 samples and BiVO4 powders confirm the involvement of hydroxyl radicals and the separation efficiency of electron-hole pairs in MB photocatalytic degradation. Besides, the T-BVO-600 exhibits good recyclability for MB removal, achieving a removal rate of above 83% after five cycles. The T-BVO-600 has the features of high efficiency and good recyclability for MB photocatalytic degradation. These results provide new insight into the purpose of improving the photocatalytic activity of BiVO4 catalyst.

Photocatalytic degradation of methylene blue from aqueous solutions using nanopillars-TiO2 thin films: Batch reactor studies

2018 ◽  
Vol 18 (3) ◽  
pp. 81-91 ◽  
Author(s):  
C. Lalhriatpuia
Keyword(s):  
Thin Films ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Organic Carbon ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

Nanopillars-TiO2 thin films was obtained on a borosilicate glass substrate with (S1) and without (S2) polyethylene glycol as template. The photocatalytic behaviour of S1 and S2 thin films was assessed inthe degradation of methylene blue (MB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the SEM, XRD, FTIR and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data confirmed that the TiO2 particles are in its anatase mineral phase. The SEM and AFM images indicated the catalyst is composed with nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of MB was well studied at wide range of physico-chemical parameters. The effect of solution pH (pH 4.0 to 10.0) and MB initial concentration (1.0 to 10.0 mg/L) was extensively studied and the effect of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of MB was demonstrated. The maximum percent removal of MB was observed at pH 8.0 beyond which it started decreasing and a low initial concentration of the pollutant highly favoured the photocatalytic degradation using thin films and the presence of several interfering ions diminished the photocatalytic activity of thin films to some extent. The overall photocatalytic activity was in the order: S2 > S1 > UV. The photocatalytic degradation of MB was followed the pseudo-first-order rate kinetics. The mineralization of MB was studied with total organic carbon measurement using the TOC (total organic carbon) analysis.

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