scholarly journals Use of Barium Chromate in Photocatalytic Degradation of Eosin Yellow

2020 ◽  
Vol 20 (2) ◽  
pp. 924-933 ◽  
Author(s):  
D. Rani Rosaline ◽  
S. S. R. Inbanathan ◽  
A. Suganthi ◽  
M. Rajarajan ◽  
G. Kavitha ◽  
...  

2018 ◽  
Vol 11 (3) ◽  
pp. 1311-1319
Author(s):  
Dinesh I. Prajapati ◽  
Hari Shankar Sharma ◽  
Rakshit Ameta

2021 ◽  
Vol 19 (9) ◽  
pp. 81-87
Author(s):  
Hind I. Hussein ◽  
Firas H. Abdulrazzak

TiO2 was synthesized in this work by chemical route, when the titanium oxysulfato (TiOSO4) react with 4:6 H2O2/H2O after is dissolved in deionized water. The yellow precipitate was drying at 100oC before heat treated at 400°C to obtain crystalline TiO2. The sample were characterized using FT-IR and X-ray diffraction spectroscopy which identified that product was mixture between two form anatase and rutile. The photocatalytic activity of synthesized TiO2 was tested in the degradation of Eousin yellow which compare with two form of TiO2. Evaluated the results was shown that H2O2 was succeed to preparing TiO2 from TiOSO4 with higher activity then anatase and rutile forms.


2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
T. S. Anirudhan ◽  
S. R. Rejeena

The present study describes the feasibility of a novel adsorbent cum photocatalyst, poly(pyrrole-co-aniline)-coated TiO2/nanocellulose composite (P(Py-co-An)-TiO2/NCC), to remove eosin yellow (EY) from aqueous solutions. The removal of EY was investigated by batch adsorption followed by photocatalysis. The effect of various adsorption parameters like adsorbent dose, pH, contact time, initial concentration, and ionic strength has been optimized for treating effluents from the dye industry. Adsorption of EY reached maximum at pH 4.5 and complete removal of dye was achieved using 3.5 g/L of P(Py-co-An)-TiO2/NCC. Adsorption equilibrium data were fitted with Langmuir and Fritz-Schlunder isotherm models and the kinetics of adsorption follows a second-order mechanism. The adsorption capacity of P(Py-co-An)-TiO2/NCC was found to be 3.39 × 10−5 mol/g and reached equilibrium within 90 min. The photocatalytic degradation of adsorbed dye under sunlight was possible and about 92.3% of dye was degraded within 90 min. The reusability of P(Py-co-An)-TiO2/NCC was also investigated. The results indicate that P(Py-co-An)-TiO2/NCC is the best material for the wiping out of EY from aqueous solutions.


2018 ◽  
Vol 18 (3) ◽  
pp. 81-91 ◽  
Author(s):  
C. Lalhriatpuia

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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