Degradation of refractory organics in dual-cathode electro-Fenton using air-cathode for H2O2 electrogeneration and microbial fuel cell cathode for Fe2+ regeneration
Creators
- 1. School of Environmental Science and Engineering, Hubei Polytechnic University, Huangshi 435003 (China)
- 2. School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)
- 3. Hubei Provincial Engineering Laboratory of Solid Waste Treatment, Disposal and Recycling, 1037 Luoyu Road, Wuhan, Hubei 430074 (China)
Description
Highlights: • Dual-cathode electro-Fenton was realized by coupling air-cathode with MFC cathode. • Fe2+ regeneration was accelerated through Fe3+ reduction on CF cathode of MFC. • RhB removal rate was 64% higher than electro-Fenton without coupling MFC cathode. • MFC power generation was enhanced by 480% due to higher Fe3+/Fe2+ redox potential. The electrogeneration of H2O2 and electro-regeneration of ferrous are conflicting matters in electro-Fenton system. In this research, the degradation of Rhodamine B, methyl orange (MO) and 4-chlorophenol (4-CP) was investigated using a novel dual-cathode microbial fuel cell (MFC) electro-Fenton (EF) hybrid system. An air-cathode of an EF system was used for H2O2 electrogeneration and a carbon felt cathode of a MFC was used to accelerate Fe2+ regeneration. Synergistic improvement of MFC power generation and the degradation of the above refractory organics through EF reaction was achieved. The EF air-cathode was fabricated by adopting activated carbon/graphite powder mixture and PVDF binder, which showed higher H2O2 generation but slower Fe3+ reduction rate than MFC carbon felt cathode. The Rhodamine B removal rate constant and mineralization current efficiency of the MFC coupled EF were 64% and 42% higher than that of uncoupled EF, respectively. The MFC-EF coupled system also exhibited significantly higher removal efficiency for MO and 4-CP than that of un-coupled EF system. Moreover, the power density of MFC was greatly enhanced by coupling EF due to higher Fe3+/Fe2+ redox potential than oxygen reduction.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2021.125269Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2021.125269;
- PII
- S0304389421002326;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 412
- Journal Page Range
- vp.
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54028977
- Subject category
- S36: MATERIALS SCIENCE; S74: ATOMIC AND MOLECULAR PHYSICS;
- Descriptors DEI
- ACTIVATED CARBON; CATHODES; FUEL CELLS; GRAPHITE; HYDROGEN PEROXIDE; IRON IONS; METHYL ORANGE; MINERALIZATION; ORGANIC FLUORINE COMPOUNDS; OXYGEN; POLYVINYLS; POWDERS; POWER GENERATION; REACTION KINETICS; REDOX POTENTIAL; RHODAMINES
- Descriptors DEC
- ADSORBENTS; AMINES; AZO COMPOUNDS; AZO DYES; CARBON; CARBOXYLIC ACIDS; CHARGED PARTICLES; DIRECT ENERGY CONVERTERS; DYES; ELECTROCHEMICAL CELLS; ELECTRODES; ELEMENTS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HYDROGEN COMPOUNDS; INDICATORS; IONS; KINETICS; MINERALS; NONMETALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANIC POLYMERS; ORGANIC SULFUR COMPOUNDS; OXYGEN COMPOUNDS; PEROXIDES; POLYMERS; REAGENTS; SULFONIC ACIDS
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.