Photocatalytic degradation of an azo dye in a tubular continuous-flow photoreactor with immobilized TiO"2 on glass plates [An article from: Chemical Engineering Journal]
Book Details
PublisherElsevier
ISBN / ASINB000PDT9Z4
ISBN-13978B000PDT9Z3
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Chemical Engineering Journal, published by Elsevier in 2007. 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 photocatalytic degradation of C.I. Acid Red 27 (AR27), an anionic monoazo dye of acid class, in aqueous solutions was investigated in a tubular continuous-flow photoreactor with immobilized TiO"2 on glass plates. The removal percent is a function of photoreactor length, volumetric flow rate and light intensity. The removal efficiency increases as the light intensity increases but it decreases when the flow rate is increased. The AR27 degradation was followed through HPLC, UV-vis and chemical oxygen demand (COD) analyses. The results of these analyses showed that the final outlet stream from the photoreactor was considerably mineralized. NH"4^+, NO"3^-, NO"2^- and SO"4^2^- ions were analyzed as mineralization products of nitrogen and sulfur heteroatoms, respectively. Results show that the final concentration of SO"4^2^- ions and N-containing mineralization products are less than the final expected stoichiometric values. Based on the results obtained in present and previous studies, a reaction pathway for the photocatalytic degradation of AR27 is proposed. The kinetic analysis of the decolorization of AR27 in continuous-mode shows a pseudo-first-order reaction. Results show that a linear relation exists between pseudo-first-order reaction rate constant and reciprocal of volumetric flow rate.
Description:
The photocatalytic degradation of C.I. Acid Red 27 (AR27), an anionic monoazo dye of acid class, in aqueous solutions was investigated in a tubular continuous-flow photoreactor with immobilized TiO"2 on glass plates. The removal percent is a function of photoreactor length, volumetric flow rate and light intensity. The removal efficiency increases as the light intensity increases but it decreases when the flow rate is increased. The AR27 degradation was followed through HPLC, UV-vis and chemical oxygen demand (COD) analyses. The results of these analyses showed that the final outlet stream from the photoreactor was considerably mineralized. NH"4^+, NO"3^-, NO"2^- and SO"4^2^- ions were analyzed as mineralization products of nitrogen and sulfur heteroatoms, respectively. Results show that the final concentration of SO"4^2^- ions and N-containing mineralization products are less than the final expected stoichiometric values. Based on the results obtained in present and previous studies, a reaction pathway for the photocatalytic degradation of AR27 is proposed. The kinetic analysis of the decolorization of AR27 in continuous-mode shows a pseudo-first-order reaction. Results show that a linear relation exists between pseudo-first-order reaction rate constant and reciprocal of volumetric flow rate.
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