Published March 1, 2013 | Version v1
Journal article

Bioelectrocatalytic dechlorination of trichloroacetic acid at gel-immobilized hemoglobin on multiwalled carbon nanotubes modified graphite electrode: Kinetic modeling and reaction pathways

  • 1. Research Center of Environmental Engineering, Zhejiang University of Technology, Hangzhou 310032, Zhejiang (China)
  • 2. College of Life and Environmental Science, Hangzhou Normal University, Hangzhou 310036, Zhejiang (China)
  • 3. College of Chemical Engineering and Materials, Zhejiang University of Technology, Hangzhou 310032, Zhejiang (China)
  • 4. College of Biological and Environmental Engineering, Zhejiang University of Technology, Hangzhou 310032, Zhejiang (China)

Description

Highlights: ► The electrons transfer from enzyme in the electrode to COCs was the key step. ► The average current efficiency was influenced by pH and temperature of the systems. ► The most favourable degradation conditions for TCA were found to be pH 3 and 310 K. ► The activation energy of 26.2 kJ mol−1 was also calculated by the Arrhenius equation. ► Bioelectrocatalytic mechanism of TCA was verified by kinetic expressions. -- Abstract: In bioelectrochemically reductive dechlorination of chlorinated organic compounds (COCs), the electrons transfer from enzyme in the electrode to COCs was the key step, which determined the average current efficiency (CE) and was influenced by the pH and temperature of the systems. In this work, the effect of temperature (288–318 K) and pH (2–11) of the electrolyte on decholrination of trichloroacetic acid (TCA) was investigated in the sodium alginate/hemoglobin-multiwalled carbon nanotubes-graphite composite electrode (Hb/SA–MWCNT–GE). The results showed that the most favourable degradation conditions for TCA by Hb/SA–MWCNT–GE were found to be pH 3 and 310 K. By varying the pH of the systems, it was found that a proton accompanied with an electron transfer between the electrode and heme Fe(III)/Fe(II) of Hb during the reaction. Additionally, the activation energy of 26.2 kJ mol−1 was also calculated by the Arrhenius equation for the reaction. The total mass balance of the reactant and the products was in the range of 97–105% during the bioelectrochemically reductive reaction. The CE only decreased from 87% to 83% when the Hb/SA–MWCNT–GE was used 5 times. Based on the intermediates detected, a pathway was proposed for TCA degradation in which it underwent dechlorination process. The main degradation mechanism described by a parallel reaction rather than by a sequential reaction for dechlorination of TCA in Hb/SA–MWCNT–GE system was proposed. These data provided relevant information about the applicability of bioelectrocatalytic systems for treatment of wastewater contaminated by COCs

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2013.01.015

Additional details

Identifiers

DOI
10.1016/j.electacta.2013.01.015;
PII
S0013-4686(13)00034-0;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
92
Journal Page Range
p. 153-160
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

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