Electrical Energy Generation by Microbial Fuel Cells With Microalgae on the Cathode
DOI:
https://doi.org/10.20535/ibb.2024.8.1.290311Keywords:
microbial fuel cell, biofilm, bioanode, biocathode, microalgaeAbstract
Background. The possibility of converting organic compounds into electrical energy in microbial fuel cells (MFCs) makes MFCs a promising eco-friendly technology. However, the use of platinum or hexacyanoferrates may increase costs or lead to secondary environmental pollution. The use of microalgae in the cathode chamber is a promising solution to these problems.
Objective. We aimed to establish the dependence of electrical energy generation and the efficiency of the application of a specific type of algae on the type and mode of lighting.
Methods. In the study, two-chamber H-type MFC with salt bridge was used. Fermented residue after methanogenesis was used as inoculum in the anode chamber, and microalgae cultures Chlorella vulgaris, Desmodesmus armatus, and Parachlorella kessleri were used as inoculum in the cathode chamber.
Results. MFCs with microalgae demonstrate the ability to generate current under different light sources. The maximum voltage for the MFC with an anode biofilm and with microalgae in the cathode chamber is 13–15% lower compared to the MFC with an abiotic cathode (840 ± 42 mV). The maximum current is 2–6% lower than the control (480 ± 24 mA) for the MFC with Chlorella vulgaris and the MFC with Parachlorella kessleri, and 8% higher for the MFC with Desmodesmus armatus compared to the MFC with an abiotic cathode. The MFCs with microalgae are capable of generating electrical energy for an extended period.
Conclusions. With a pre-grown anodic biofilm, both the current and voltage maintain relative stability when the light source is changed. The potential use of solar lighting broadens the applicability of the MFCs with microalgae, as it eliminates the need for additional costs associated with artificial light sources.
References
The Paris Agreement – Publication [Internet]. United nationos Climate Change [cited 2023 Aug 7]. Available from: https://unfccc.int/documents/184656
Christwardana M, Hadiyanto H, Motto SA, Sudarno S, Haryani K. Performance evaluation of yeast-assisted microalgal microbial fuel cells on bioremediation of cafeteria wastewater for electricity generation and microalgae biomass production. Biomass Bioenergy. 2020;139(105617):105617. DOI: 10.1016/j.biombioe.2020.105617
Gude VG. Wastewater treatment in microbial fuel cells – an overview. J Clean Prod. 2016;122:287-307. DOI: 10.1016/j.jclepro.2016.02.022
Kakarla R, Min B. Photoautotrophic microalgae Scenedesmus obliquus attached on a cathode as oxygen producers for microbial fuel cell (MFC) operation. Int J Hydrogen Energy. 2014;39(19):10275-83. DOI: 10.1016/j.ijhydene.2014.04.158
Huang L, Regan JM, Quan X. Electron transfer mechanisms, new applications, and performance of biocathode microbial fuel cells. Bioresour Technol. 2011;102(1):316-23. DOI: 10.1016/j.biortech.2010.06.096
Arun S, Sinharoy A, Pakshirajan K, Lens PNL. Algae based microbial fuel cells for wastewater treatment and recovery of value-added products. Renew Sustain Energy Rev. 2020;132(110041):110041. DOI: 10.1016/j.rser.2020.110041
Saratale RG, Kuppam C, Mudhoo A, Saratale GD, Periyasamy S, Zhen G, et al. Bioelectrochemical systems using microalgae – A concise research update. Chemosphere. 2017;177:35-43. DOI: 10.1016/j.chemosphere.2017.02.132
Enamala MK, Dixit R, Tangellapally A, Singh M, Dinakarrao SMP, Chavali M, et al. Photosynthetic microorganisms (Algae) mediated bioelectricity generation in microbial fuel cell: Concise review. Environ Technol Innov. 2020;19(100959):100959. DOI: 10.1016/j.eti.2020.100959
Bazdar E, Roshandel R, Yaghmaei S, Mardanpour MM. The effect of different light intensities and light/dark regimes on the performance of photosynthetic microalgae microbial fuel cell. Bioresour Technol. 2018;261:350-60. DOI: 10.1016/j.biortech.2018.04.026
Yahampath Arachchige Don CDY, Babel S. Comparing the performance of microbial fuel cell with mechanical aeration and photosynthetic aeration in the cathode chamber. Int J Hydrogen Energy. 2021;46(31):16751-61. DOI: 10.1016/j.ijhydene.2020.09.068
Shchurska K, Kuzminskyi Y. Bioelectrochemical generation of hydrogen in a microbial fuel cell. 3. Experimental part. Vidnovluvana Energetika. 2012;(1):67-77.
Kokabian B, Ghimire U, Gude VG. Water deionization with renewable energy production in microalgae - microbial desalination process. Renewable Energy. 2018;122:354-61. DOI: 10.1016/j.renene.2018.01.061
Lawson K, Rossi R, Regan JM, Logan BE. Impact of cathodic electron acceptor on microbial fuel cell internal resistance. Biores Technol. 2020;316:123919. DOI: 10.1016/j.biortech.2020.123919
Liu Q, Yang Y, Mei X, Liu B, Chen C, Xing D. Response of the microbial community structure of biofilms to ferric iron in microbial fuel cells. Science of The Total Environment. 2018;631-632:695-701. DOI: 10.1016/j.scitotenv.2018.03.008
Koltysheva D, Shchurska K, Kuzminskyi Y. Anode biofilm formation with applied external voltage. Innov Biosyst Bioeng. 2023;7(1):14-23. DOI: 10.20535/ibb.2023.7.1.273816
Borysova OV, Tsarenko PM, Konishchuk MO. Microalgae of culture collection of IBASU-A of M.G. Kholodny Institute of Botany NAS of Ukraine. Kyiv: M.G. Kholodny Institute of Botany NAS of Ukraine; 2014. 110 p.
Golub NB, Shinkarchuk MV, Kozlovets OA, Morgun BV, Lakhneko OR, Stepanenko AI, et al. Determination of biogas producers in antibiotic-containing sewage. Water Air Soil Pollut. 2020;231(8). DOI: 10.1007/s11270-020-04805-6
Flores-Rodriguez C, Min B. Enrichment of specific microbial communities by optimum applied voltages for enhanced methane production by microbial electrosynthesis in anaerobic digestion. Bioresour Technol. 2020;300:122624. DOI: 10.1016/j.biortech.2019.122624
Cai W, Liu W, Zhang Z, Feng K, Ren G, Pu C, et al. Electro-driven methanogenic microbial community diversity and variability in the electron abundant niche. Sci Total Environ. 2019;661:178-86. DOI: 10.1016/j.scitotenv.2019.01.131
Wati A, Rusva R, Umar L. Effect of LED wavelengths and light-dark cycle on photosynthetic production of Chlorella kessleri for algae-based biosensor optimization. J Phys. 2019;1351:012003. DOI: 10.1088/1742-6596/1351/1/012003
Baidya A, Akter T, Islam MR, Shah AK, Hossain MA, Salam MA, et al. Effect of different wavelengths of LED light on the growth, chlorophyll, β-carotene content and proximate composition of Chlorella ellipsoidea. Heliyon. 2021;7(12):e08525. DOI: 10.1016/j.heliyon.2021.e08525
Luimstra VM, Schuurmans JM, Verschoor AM, Hellingwerf KJ, Huisman J, Matthijs HC. Blue light reduces photosynthetic efficiency of cyanobacteria through an imbalance between photosystems I and II. Photosynth Res. 2018;138(2):177-89. DOI: 10.1007/s11120-018-0561-5
Koc C, Kommareddy A, Anderson GA. Use of red and blue light-emitting diodes (LED) and fluorescent lamps to grow microalgae in a photobioreactor. Isr J Aquac Bamidgeh. 2013;65. DOI: 10.46989/001c.20661
González del Campo A, Cañizares P, Rodrigo MA, Fernández FJ, Lobato J. Microbial fuel cell with an algae-assisted cathode: A preliminary assessment. J Power Sources. 2013;242:638-45. DOI: 10.1016/j.jpowsour.2013.05.110
Search BioNumbers - the database of useful biological numbers [Internet]. Harvard.edu. [cited 2023 Aug 7]. Available from: https://bionumbers.hms.harvard.edu
Yadav G, Sharma I, Ghangrekar M, Sen R. A live bio-cathode to enhance power output steered by bacteria-microalgae synergistic metabolism in microbial fuel cell. J Power Sour. 2020; 449:227560. DOI: 10.1016/j.jpowsour.2019.227560
Koltysheva D, Shchurska K, Kuzminskyi Y. Microalgae and cyanobacteria as biological agents of biocathodes in biofuel cells. BioTechnologia. 2021;102(4):437-44. DOI: 10.5114/bta.2021.111108
Angioni S, Millia L, Mustarelli P, Doria E, Temporiti ME, Mannucci B, et al. Photosynthetic microbial fuel cell with polybenzimidazole membrane: synergy between bacteria and algae for wastewater removal and biorefinery. Heliyon. 2018;4(3):e00560. DOI: 10.1016/j.heliyon.2018.e00560
Sivakumar P, Ilango K, Praveena N, Sircar A, Balasubramanian R, Sakthisaravanan A, et al. Algal fuel cell. In: Jacob-Lopes E, Zepka LQ, Queiroz MI, editors. Microalgal biotechnology. IntechOpen; 2018. DOI: 10.5772/intechopen.74285
Wang DB, Song TS, Guo T, Zeng Q, Xie J. Electricity generation from sediment microbial fuel cells with algae-assisted cathodes. Int J Hydrogen Energy. 2014;39(25):13224-30. DOI: 10.1016/j.ijhydene.2014.06.141
Wang X, Feng Y, Liu J, Lee H, Li C, Li N, et al. Sequestration of CO2 discharged from anode by algal cathode in microbial carbon capture cells (MCCs). Biosens Bioelectron. 2010;25(12):2639-43. DOI: 10.1016/j.bios.2010.04.036
Venkata Mohan S, Srikanth S, Chiranjeevi P, Arora S, Chandra R. Algal biocathode for in situ terminal electron acceptor (TEA) production: Synergetic association of bacteria–microalgae metabolism for the functioning of biofuel cell. Bioresour Technol. 2014;166:566-74. DOI: 10.1016/j.biortech.2014.05.081
Wu YC, Wang ZJ, Zheng Y, Xiao Y, Yang ZH, Zhao F. Light intensity affects the performance of photo microbial fuel cells with Desmodesmus sp. A8 as cathodic microorganism. Appl Energy. 2014;116:86-90. DOI: 10.1016/j.apenergy.2013.11.066
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Dina Koltysheva, Kateryna Shchurska, Yevhenii Kuzminskyi
This work is licensed under a Creative Commons Attribution 4.0 International License.
The ownership of copyright remains with the Authors.
Authors may use their own material in other publications provided that the Journal is acknowledged as the original place of publication and National Technical University of Ukraine “Igor Sikorsky Kyiv Polytechnic Institute” as the Publisher.
Authors are reminded that it is their responsibility to comply with copyright laws. It is essential to ensure that no part of the text or illustrations have appeared or are due to appear in other publications, without prior permission from the copyright holder.
IBB articles are published under Creative Commons licence:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under CC BY 4.0 that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.