Degradation of Evans Blue diazo dye by electrochemical processes based on Fenton's reaction chemistry

Vanessa S. Antonin, Sergio GARCIA SEGURA, Mauro C. Santos, Enric Brillas

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Abstract A solution with 0.245 mM of the diazo dye Evans Blue and 0.50 mM Fe2+ as catalyst of pH 3.0 was comparatively degraded by electrochemical processes based on Fenton's reaction chemistry like electro-Fenton (EF), photoelectro-Fenton (PEF) with a 6 W UVA light and solar photoelectro-Fenton (SPEF). Electrolytic trials were made in a 100 mL stirred tank reactor with a boron-doped diamond (BDD) anode and an air-diffusion cathode at constant current density. Organics were destroyed by ·OH produced at the anode surface from water oxidation and in the bulk from Fenton's reaction between added Fe2+ and H2O2 generated at the cathode. Evans Blue decay obeyed a pseudo-first-order kinetics and was much faster than solution decolorization due to the formation of colored aromatic products. The mineralization rate rose in the sequence EF < PEF < SPEF. Almost total mineralization was rapidly achieved in SPEF at current density ≥66.7 mA cm-2 because of the potent UV radiation from sunlight. Up to 19 aromatic intermediates and 16 hydroxylated derivatives including diazo, monoazo, biphenylic, benzenic, naphthalenic and phthalic acid compounds were detected by LC-MS. The SPEF process was performed in a 10 L flow plant with a Pt/air-diffusion cell coupled to a CPC photoreactor in order to confirm its viability at industrial scale. 88% mineralization with 42% current efficiency and 2.13 kWh kg-1 DOC energy consumption were obtained after 300 min of treatment at 55.4 mA cm-2. Nine short-linear carboxylic acids were identified as final products, oxalic, formic and oxamic acids being the most persistent. The photodecarboxylation of Fe(III)-carboxylate complexes explained the good oxidation ability of PEF and SPEF. The initial S of the diazo dye was transformed into SO4 2- ion, whereas its initial N was mineralized to NO3 - ion but largely lost as N-volatile products.

Original languageEnglish (US)
Article number2061
Pages (from-to)1-11
Number of pages11
JournalJournal of Electroanalytical Chemistry
Volume747
DOIs
StatePublished - Jun 15 2015
Externally publishedYes

Fingerprint

Evans Blue
Oxamic Acid
Anodes
Cathodes
Coloring Agents
Current density
Dyes
Ions
Degradation
Oxidation
Diamond
Boron
Acids
Carboxylic Acids
Air
Carboxylic acids
Ultraviolet radiation
Diamonds
Energy utilization
Derivatives

Keywords

  • Boron-doped diamond
  • Electro-Fenton
  • Evans Blue
  • Hydroxyl radical
  • Oxidation products
  • Solar photoelectro-Fenton

ASJC Scopus subject areas

  • Analytical Chemistry
  • Chemical Engineering(all)
  • Electrochemistry

Cite this

Degradation of Evans Blue diazo dye by electrochemical processes based on Fenton's reaction chemistry. / Antonin, Vanessa S.; GARCIA SEGURA, Sergio; Santos, Mauro C.; Brillas, Enric.

In: Journal of Electroanalytical Chemistry, Vol. 747, 2061, 15.06.2015, p. 1-11.

Research output: Contribution to journalArticle

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abstract = "Abstract A solution with 0.245 mM of the diazo dye Evans Blue and 0.50 mM Fe2+ as catalyst of pH 3.0 was comparatively degraded by electrochemical processes based on Fenton's reaction chemistry like electro-Fenton (EF), photoelectro-Fenton (PEF) with a 6 W UVA light and solar photoelectro-Fenton (SPEF). Electrolytic trials were made in a 100 mL stirred tank reactor with a boron-doped diamond (BDD) anode and an air-diffusion cathode at constant current density. Organics were destroyed by ·OH produced at the anode surface from water oxidation and in the bulk from Fenton's reaction between added Fe2+ and H2O2 generated at the cathode. Evans Blue decay obeyed a pseudo-first-order kinetics and was much faster than solution decolorization due to the formation of colored aromatic products. The mineralization rate rose in the sequence EF < PEF < SPEF. Almost total mineralization was rapidly achieved in SPEF at current density ≥66.7 mA cm-2 because of the potent UV radiation from sunlight. Up to 19 aromatic intermediates and 16 hydroxylated derivatives including diazo, monoazo, biphenylic, benzenic, naphthalenic and phthalic acid compounds were detected by LC-MS. The SPEF process was performed in a 10 L flow plant with a Pt/air-diffusion cell coupled to a CPC photoreactor in order to confirm its viability at industrial scale. 88{\%} mineralization with 42{\%} current efficiency and 2.13 kWh kg-1 DOC energy consumption were obtained after 300 min of treatment at 55.4 mA cm-2. Nine short-linear carboxylic acids were identified as final products, oxalic, formic and oxamic acids being the most persistent. The photodecarboxylation of Fe(III)-carboxylate complexes explained the good oxidation ability of PEF and SPEF. The initial S of the diazo dye was transformed into SO4 2- ion, whereas its initial N was mineralized to NO3 - ion but largely lost as N-volatile products.",
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T1 - Degradation of Evans Blue diazo dye by electrochemical processes based on Fenton's reaction chemistry

AU - Antonin, Vanessa S.

AU - GARCIA SEGURA, Sergio

AU - Santos, Mauro C.

AU - Brillas, Enric

PY - 2015/6/15

Y1 - 2015/6/15

N2 - Abstract A solution with 0.245 mM of the diazo dye Evans Blue and 0.50 mM Fe2+ as catalyst of pH 3.0 was comparatively degraded by electrochemical processes based on Fenton's reaction chemistry like electro-Fenton (EF), photoelectro-Fenton (PEF) with a 6 W UVA light and solar photoelectro-Fenton (SPEF). Electrolytic trials were made in a 100 mL stirred tank reactor with a boron-doped diamond (BDD) anode and an air-diffusion cathode at constant current density. Organics were destroyed by ·OH produced at the anode surface from water oxidation and in the bulk from Fenton's reaction between added Fe2+ and H2O2 generated at the cathode. Evans Blue decay obeyed a pseudo-first-order kinetics and was much faster than solution decolorization due to the formation of colored aromatic products. The mineralization rate rose in the sequence EF < PEF < SPEF. Almost total mineralization was rapidly achieved in SPEF at current density ≥66.7 mA cm-2 because of the potent UV radiation from sunlight. Up to 19 aromatic intermediates and 16 hydroxylated derivatives including diazo, monoazo, biphenylic, benzenic, naphthalenic and phthalic acid compounds were detected by LC-MS. The SPEF process was performed in a 10 L flow plant with a Pt/air-diffusion cell coupled to a CPC photoreactor in order to confirm its viability at industrial scale. 88% mineralization with 42% current efficiency and 2.13 kWh kg-1 DOC energy consumption were obtained after 300 min of treatment at 55.4 mA cm-2. Nine short-linear carboxylic acids were identified as final products, oxalic, formic and oxamic acids being the most persistent. The photodecarboxylation of Fe(III)-carboxylate complexes explained the good oxidation ability of PEF and SPEF. The initial S of the diazo dye was transformed into SO4 2- ion, whereas its initial N was mineralized to NO3 - ion but largely lost as N-volatile products.

AB - Abstract A solution with 0.245 mM of the diazo dye Evans Blue and 0.50 mM Fe2+ as catalyst of pH 3.0 was comparatively degraded by electrochemical processes based on Fenton's reaction chemistry like electro-Fenton (EF), photoelectro-Fenton (PEF) with a 6 W UVA light and solar photoelectro-Fenton (SPEF). Electrolytic trials were made in a 100 mL stirred tank reactor with a boron-doped diamond (BDD) anode and an air-diffusion cathode at constant current density. Organics were destroyed by ·OH produced at the anode surface from water oxidation and in the bulk from Fenton's reaction between added Fe2+ and H2O2 generated at the cathode. Evans Blue decay obeyed a pseudo-first-order kinetics and was much faster than solution decolorization due to the formation of colored aromatic products. The mineralization rate rose in the sequence EF < PEF < SPEF. Almost total mineralization was rapidly achieved in SPEF at current density ≥66.7 mA cm-2 because of the potent UV radiation from sunlight. Up to 19 aromatic intermediates and 16 hydroxylated derivatives including diazo, monoazo, biphenylic, benzenic, naphthalenic and phthalic acid compounds were detected by LC-MS. The SPEF process was performed in a 10 L flow plant with a Pt/air-diffusion cell coupled to a CPC photoreactor in order to confirm its viability at industrial scale. 88% mineralization with 42% current efficiency and 2.13 kWh kg-1 DOC energy consumption were obtained after 300 min of treatment at 55.4 mA cm-2. Nine short-linear carboxylic acids were identified as final products, oxalic, formic and oxamic acids being the most persistent. The photodecarboxylation of Fe(III)-carboxylate complexes explained the good oxidation ability of PEF and SPEF. The initial S of the diazo dye was transformed into SO4 2- ion, whereas its initial N was mineralized to NO3 - ion but largely lost as N-volatile products.

KW - Boron-doped diamond

KW - Electro-Fenton

KW - Evans Blue

KW - Hydroxyl radical

KW - Oxidation products

KW - Solar photoelectro-Fenton

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