Electrochemically-mediated membrane separations for carbon dioxide capture
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2016.
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| Other Authors: | |
| Format: | Thesis |
| Language: | eng |
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Massachusetts Institute of Technology
2016
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| Online Access: | http://hdl.handle.net/1721.1/104214 |
| _version_ | 1811086306656124928 |
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| author | Vicari, Kristin Jenise |
| author2 | T. Alan Hatton. |
| author_facet | T. Alan Hatton. Vicari, Kristin Jenise |
| author_sort | Vicari, Kristin Jenise |
| collection | MIT |
| description | Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2016. |
| first_indexed | 2024-09-23T13:24:05Z |
| format | Thesis |
| id | mit-1721.1/104214 |
| institution | Massachusetts Institute of Technology |
| language | eng |
| last_indexed | 2024-09-23T13:24:05Z |
| publishDate | 2016 |
| publisher | Massachusetts Institute of Technology |
| record_format | dspace |
| spelling | mit-1721.1/1042142019-04-12T15:58:18Z Electrochemically-mediated membrane separations for carbon dioxide capture Vicari, Kristin Jenise T. Alan Hatton. Massachusetts Institute of Technology. Department of Chemical Engineering. Massachusetts Institute of Technology. Department of Chemical Engineering. Chemical Engineering. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2016. Cataloged from PDF version of thesis. Includes bibliographical references (pages 134-142). This thesis describes and analyzes several new designs for carbon dioxide (CO₂) separations using quinones in electrochemical cells. The intended application is carbon capture and sequestration. A quinone-ferrocene electrolyte is proposed as a novel chemistry for electrochemical carbon capture. Quantitative analyses are presented for two designs, and experimental results are provided for the quinone-ferrocene system in two configurations. The first design uses quinones for facilitated transport of CO₂ across a planar, supported liquid membrane. A mixture of quinone and dianion adduct is sandwiched between two porous electrodes. An analytical solution for the current-potential equation is derived and then used to quantify the expected performance of the system in terms of capacity and energy efficiency. In the second design, the electrolyte flows between the two planar electrodes of the electrochemical cell. Quinone reacts at the porous cathode to absorb CO₂ from the gas phase. The dianion adduct reacts at the nonporous anode to desorb the CO₂ , which produces supersaturated regions in the cell. The CO₂ evaporates and the electrolyte is recycled. A numerical model has been developed to solve for the spatial values of species concentrations, current, and ionic potential in the flowing electrolyte. A design analysis of this system highlights the quantitative impact of certain operating parameters and supports recommendations for future development. The first demonstration of an electrolyte that uses a quinone-ferrocene redox couple for carbon capture in a flow cell is presented. The quinone and ferrocene chemistries are introduced, and experimental results highlight the ability to couple quinone reduction to ferrocene oxidation and ferrocenium reduction to dianion-adduct oxidation using graphite electrodes. A bench-scale test cell has been designed and built to demonstrate electrochemical carbon capture in a cell with laminar flow of the electrolyte. The quinone-ferrocene couple is implemented in this flow design. Experimental results show the ability to continuously capture CO₂ from a gas stream (15% CO₂, 85% nitrogen (N₂)) using the quinone-ferrocene couple in this design. Finally, experimental results highlight the cycling of electrochemical absorption and desorption of carbon dioxide using the quinone-ferrocene chemistry in flow-through electrodes. by Kristin Jenise Vicari. Ph. D. 2016-09-13T19:13:20Z 2016-09-13T19:13:20Z 2016 2016 Thesis http://hdl.handle.net/1721.1/104214 958140016 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 167 pages application/pdf Massachusetts Institute of Technology |
| spellingShingle | Chemical Engineering. Vicari, Kristin Jenise Electrochemically-mediated membrane separations for carbon dioxide capture |
| title | Electrochemically-mediated membrane separations for carbon dioxide capture |
| title_full | Electrochemically-mediated membrane separations for carbon dioxide capture |
| title_fullStr | Electrochemically-mediated membrane separations for carbon dioxide capture |
| title_full_unstemmed | Electrochemically-mediated membrane separations for carbon dioxide capture |
| title_short | Electrochemically-mediated membrane separations for carbon dioxide capture |
| title_sort | electrochemically mediated membrane separations for carbon dioxide capture |
| topic | Chemical Engineering. |
| url | http://hdl.handle.net/1721.1/104214 |
| work_keys_str_mv | AT vicarikristinjenise electrochemicallymediatedmembraneseparationsforcarbondioxidecapture |