TY - JOUR
T1 - Heterogeneous photo-catalysis system for the degradation of azo dye Reactive Black 5 (RB5)
AU - Huang, Yao Hui
AU - Wei, Hau Cheng
AU - Chen, Hung Ta
PY - 2012/2/1
Y1 - 2012/2/1
N2 - This study investigated a heterogeneous photo-catalysis system by introducing a novel brick supported iron oxide (denoted as B1) for the heterogeneous photoassisted degradation of Reactive Black 5 (RB5) at pH value from 3 to 7 in a three-phase (gas-liquid-solid) fluidized bed reactor (3P-FBR). Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray powder diffraction (XRD) and N 2 adsorption/desorption were used to characterize the B1 catalyst. The in situ formation of hydrogen peroxide and the depletion of oxalic acid by photochemical cycle of Fe(III)- oxalate complex under UVA light (λ = 365 nm) were studied. The effects of the solution pH and the concentration of oxalic acid on the degradation of RB5 are elucidated. About 90% decolourization was measured and 80% of the total organic carbon (TOC) was eliminated at pH 5.0 after 120 min for 20 mg/L RB5 in presence of 10 g/L B1 catalyst, 30 mg/L oxalic acid under 15 W UVA light. A mechanism for the photocatalytic degradation of RB5 over B1 catalyst is proposed.
AB - This study investigated a heterogeneous photo-catalysis system by introducing a novel brick supported iron oxide (denoted as B1) for the heterogeneous photoassisted degradation of Reactive Black 5 (RB5) at pH value from 3 to 7 in a three-phase (gas-liquid-solid) fluidized bed reactor (3P-FBR). Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray powder diffraction (XRD) and N 2 adsorption/desorption were used to characterize the B1 catalyst. The in situ formation of hydrogen peroxide and the depletion of oxalic acid by photochemical cycle of Fe(III)- oxalate complex under UVA light (λ = 365 nm) were studied. The effects of the solution pH and the concentration of oxalic acid on the degradation of RB5 are elucidated. About 90% decolourization was measured and 80% of the total organic carbon (TOC) was eliminated at pH 5.0 after 120 min for 20 mg/L RB5 in presence of 10 g/L B1 catalyst, 30 mg/L oxalic acid under 15 W UVA light. A mechanism for the photocatalytic degradation of RB5 over B1 catalyst is proposed.
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U2 - 10.2166/wst.2012.202
DO - 10.2166/wst.2012.202
M3 - Article
C2 - 22233898
AN - SCOPUS:84863076749
SN - 0273-1223
VL - 65
SP - 221
EP - 226
JO - Water Science and Technology
JF - Water Science and Technology
IS - 2
ER -