Published February 15, 2013 | Version v1
Journal article

The oxidation of acid azo dye AY 36 by a manganese oxide containing mine waste

  • 1. Department of Soil Science, Stellenbosch University, P/Bag X1, Matieland 7602 (South Africa)
  • 2. Department of Chemistry, Naresuan University, Phitsanulok (Thailand)
  • 3. School of Engineering, Durham University (United Kingdom)

Description

Highlights: ► This study looks at the oxidative breakdown of the amine containing dye acid yellow 36 by a Mn oxide containing mine waste. ► The oxidation proceeds by successive one electron transfers between the dye molecule and the Mn oxide minerals. ► The initial decolorization of the dye is rapid, but does not involve the cleavage of the azo bond. -- Abstract: The oxidative breakdown of acid azo dye acid yellow 36 (AY 36) by a Mn oxide containing mine tailings is demonstrated. The oxidation reaction is pH dependent with the rate of decolorization increasing with decreasing pH. The oxidation reaction mechanism is initiated at the amino moiety and proceeds via successive, one electron transfers from the dye to the Mn oxide minerals. The reaction pathway involves the formation of a number of colorless intermediate products, some of which hydrolyze in a Mn oxide-independent step. Decolorization of the dye is rapid and is observed before the cleavage of the azo-bond, which is a slower process. The terminal oxidation products were observed to be p-benzoquinone and 3-hydroxybenzenesulfonate. The reaction order of the initial decolorization was determined to be pseudo fractional order with respect to pH and pseudo first order with respect to dye concentration and Mn tailings' surface area

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2012.12.018

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2012.12.018;
PII
S0304-3894(12)01185-5;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
246-247
Journal Page Range
p. 310-318
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.