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Photodegradation of Reactive Black 5, Direct Red 28 and Direct Yellow 12 using UV, UV/H"2O"2 and UV/H"2O"2/Fe^2^+: a comparative study [An article from: Journal of Hazardous Materials]
Book Details
Author(s)U. Bali, E. Catalkaya, F. Sengul
PublisherElsevier
ISBN / ASINB000RR13I4
ISBN-13978B000RR13I6
AvailabilityAvailable for download now
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Journal of Hazardous Materials, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
The photodegradation of three commercially available dyestuffs (C.I. Reactive Black 5, C.I. RB5, C.I. Direct Yellow 12, C.I. DY12, and C.I. Direct Red 28, C.I. DR28) by UV, UV/H"2O"2 and UV/H"2O"2/Fe(II) processes was investigated in a laboratory-scale batch photoreactor equipped with an 16W immersed-type low-pressure mercury vapour lamp. The experimental results were assessed in terms of absorbance and total organic carbon (TOC) reduction. The initial concentration was kept constant at 100mgl^-^1 for all dyes. Initial results showed that, color removal efficiencies by UV or H"2O"2 alone were negligible for all dyes. Almost complete disappearance of C.I. RB5 (99%) and DY12 (98%) in UV/H"2O"2 process was possible to achieve after 60min of irradiation. The maximum color removal efficiency of C.I. DR28 after 60min of irradiation, however, was only 40% and reached a maximum value of 70% after 120min of irradiation. Corresponding mineralization efficiencies were 50, 55 and 7-12%, respectively. The addition of Fe(II) to the system, so-called the photo-Fenton process, greatly enhanced the color removal, the efficiencies being 98, 88 and 85% for C.I. RB5, C.I. DY12 and C.I. DR28 only after 5min of irradiation. Corresponding mineralization efficiencies were 98% for 45min irradiation, 100% for 60min irradiation and 98% for 90min irradiation, respectively. However, marginal benefit was less significant in the higher range of both H"2O"2 and Fe(II). Furthermore, decreases in both decolorization and mineralization were observed at higher concentrations of oxidant and catalyst due to the scavenging effect of excess H"2O"2 and OH? radicals. The degradation of all dyes was found to follow first-order reaction kinetics.
Description:
The photodegradation of three commercially available dyestuffs (C.I. Reactive Black 5, C.I. RB5, C.I. Direct Yellow 12, C.I. DY12, and C.I. Direct Red 28, C.I. DR28) by UV, UV/H"2O"2 and UV/H"2O"2/Fe(II) processes was investigated in a laboratory-scale batch photoreactor equipped with an 16W immersed-type low-pressure mercury vapour lamp. The experimental results were assessed in terms of absorbance and total organic carbon (TOC) reduction. The initial concentration was kept constant at 100mgl^-^1 for all dyes. Initial results showed that, color removal efficiencies by UV or H"2O"2 alone were negligible for all dyes. Almost complete disappearance of C.I. RB5 (99%) and DY12 (98%) in UV/H"2O"2 process was possible to achieve after 60min of irradiation. The maximum color removal efficiency of C.I. DR28 after 60min of irradiation, however, was only 40% and reached a maximum value of 70% after 120min of irradiation. Corresponding mineralization efficiencies were 50, 55 and 7-12%, respectively. The addition of Fe(II) to the system, so-called the photo-Fenton process, greatly enhanced the color removal, the efficiencies being 98, 88 and 85% for C.I. RB5, C.I. DY12 and C.I. DR28 only after 5min of irradiation. Corresponding mineralization efficiencies were 98% for 45min irradiation, 100% for 60min irradiation and 98% for 90min irradiation, respectively. However, marginal benefit was less significant in the higher range of both H"2O"2 and Fe(II). Furthermore, decreases in both decolorization and mineralization were observed at higher concentrations of oxidant and catalyst due to the scavenging effect of excess H"2O"2 and OH? radicals. The degradation of all dyes was found to follow first-order reaction kinetics.
