Degradation of disperse azo dyes from waters by solar photoelectro-Fenton
- 1. Departamento de Ciencias del Ambiente, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACh, Casilla 40, Correo 33, Santiago (Chile)
- 2. Laboratori d'Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)
Description
Highlights: → Reactive azo dyes are almost totally mineralized by solar photoelectro-Fenton. → The process yields high current efficiencies and low energy consumptions. → It is more efficient and inexpensive by decreasing current and increasing dye content. → Nitrate ions are the main inorganic ions released during the mineralization process. → The process is also effective for the remediation of textile dyeing solutions. - Abstract: Solutions of the azo dyes Disperse Red 1 (DR1) and Disperse Yellow 3 (DY3), commonly used in the Chilean textile industry, in 0.1 mol dm-3 Na2SO4 and 0.5 mmol dm-3 Fe2+ of pH 3.0 were comparatively degraded by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF) using a 2.5 dm3 recirculation flow plant containing a BDD/air-diffusion cell coupled with a solar photoreactor. Organics were oxidized in EF with hydroxyl radicals formed at the anode surface from water oxidation and in the bulk from Fenton's reaction between electrogenerated H2O2 and added Fe2+. The oxidizing power of SPEF was enhanced by the additional production of hydroxyl radicals from the photolysis of Fe(III) hydrated species and the photodecomposition of Fe(III) complexes with intermediates by UV light of solar irradiation. Total decolorization, complete dye removal and almost overall mineralization for both dye solutions were only achieved using the most potent SPEF process, yielding higher current efficiencies and lower energy consumptions than EF. Final carboxylic acids like pyruvic, acetic, oxalic and oxamic were detected during the SPEF treatments. NO3- ion was released as inorganic ion. The use of a solution pH of 2.0-3.0 at 50 mA cm-2 was found preferable for SPEF. Synthetic textile dyeing solutions containing the dyes were treated under these conditions yielding lower decolorization rate, slower dye removal and smaller mineralization degree than only using 0.1 mol dm-3 Na2SO4 due to the parallel oxidation of organic dyeing components. However, lower energy consumptions were obtained by the destruction of more amounts of total organic carbon, indicating that SPEF is a useful and viable method for the remediation of textile industrial wastewaters with high contents of disperse azo dyes.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2011.05.021Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2011.05.021;
- PII
- S0013-4686(11)00741-9;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 56
- Journal Issue
- 18
- Journal Page Range
- p. 6371-6379
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 43043026
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANODES; AZO DYES; CARBON; CARBOXYLIC ACIDS; EFFICIENCY; ENERGY CONSUMPTION; HYDROGEN PEROXIDE; HYDROXYL RADICALS; IRON IONS; IRRADIATION; MINERALIZATION; NITRATES; OXIDATION; PHOTOLYSIS; REMEDIAL ACTION; SODIUM SULFATES; SOLUTIONS; ULTRAVIOLET RADIATION; VISIBLE RADIATION; WASTE WATER
- Descriptors DEC
- ALKALI METAL COMPOUNDS; AZO COMPOUNDS; CHARGED PARTICLES; CHEMICAL REACTIONS; DECOMPOSITION; DISPERSIONS; DYES; ELECTRODES; ELECTROMAGNETIC RADIATION; ELEMENTS; HOMOGENEOUS MIXTURES; HYDROGEN COMPOUNDS; IONS; LIQUID WASTES; MIXTURES; NITROGEN COMPOUNDS; NONMETALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; PEROXIDES; PHOTOCHEMICAL REACTIONS; RADIATIONS; RADICALS; SODIUM COMPOUNDS; SULFATES; SULFUR COMPOUNDS; WASTES; WATER
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.