Bioelectrocatalytic dechlorination of trichloroacetic acid at gel-immobilized hemoglobin on multiwalled carbon nanotubes modified graphite electrode: Kinetic modeling and reaction pathways
Creators
- 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.2013.01.015Additional 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
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45059772
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ACTIVATION ENERGY; ARRHENIUS EQUATION; CARBON NANOTUBES; CHLORINATED ALIPHATIC HYDROCARBONS; DECHLORINATION; EFFICIENCY; ELECTRODES; ELECTROLYTES; ELECTRON TRANSFER; ENZYMES; GRAPHITE; HEME; HEMOGLOBIN; MASS BALANCE; SIMULATION; STABILITY
- Descriptors DEC
- CARBON; CARBOXYLIC ACIDS; CHEMICAL REACTIONS; DEHALOGENATION; ELEMENTS; ENERGY; EQUATIONS; GLOBINS; HALOGENATED ALIPHATIC HYDROCARBONS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; MINERALS; NANOSTRUCTURES; NANOTUBES; NONMETALS; ORGANIC ACIDS; ORGANIC CHLORINE COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PIGMENTS; PORPHYRINS; PROTEINS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.