Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change
We describe an approach to CO 2 capture and storage from the atmosphere that involves enhancing the solubility of CO 2 in the ocean by a process equivalent to the natural silicate weathering reaction. HCl is electrochemically removed from the ocean and neutralized through reaction with silicate rock...
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American Chemical Society
2007
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ftharvardudash:oai:dash.harvard.edu:1/2794947 2023-05-15T15:52:55+02:00 Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change Aziz, Michael Schrag, Daniel House, Christopher H. House, Kurt Zenz 2007 application/pdf http://nrs.harvard.edu/urn-3:HUL.InstRepos:2794947 https://doi.org/10.1021/es0701816 en_US eng American Chemical Society http://dx.doi.org/10.1021/es0701816 Environmental Science and Technology House, Kurt Zenz, Christopher H. House, Daniel P. Schrag, and Michael J. Aziz. 2007. Electrochemical acceleration of chemical weathering as an energetically feasible approach to mitigating anthropogenic climate change. Environmental Science and Technology 41(24): 8464-8470. 0013-936X http://nrs.harvard.edu/urn-3:HUL.InstRepos:2794947 doi:10.1021/es0701816 2007 ftharvardudash https://doi.org/10.1021/es0701816 2022-04-04T12:36:08Z We describe an approach to CO 2 capture and storage from the atmosphere that involves enhancing the solubility of CO 2 in the ocean by a process equivalent to the natural silicate weathering reaction. HCl is electrochemically removed from the ocean and neutralized through reaction with silicate rocks. The increase in ocean alkalinity resulting from the removal of HCl causes atmospheric CO 2 to dissolve into the ocean where it will be stored primarily as HCO 3 − without further acidifying the ocean. On timescales of hundreds of years or longer, some of the additional alkalinity will likely lead to precipitation or enhanced preservation of CaCO 3 , resulting in the permanent storage of the associated carbon, and the return of an equal amount of carbon to the atmosphere. Whereas the natural silicate weathering process is effected primarily by carbonic acid, the engineered process accelerates the weathering kinetics to industrial rates by replacing this weak acid with HCl. In the thermodynamic limit—and with the appropriate silicate rocks—the overall reaction is spontaneous. A range of efficiency scenarios indicates that the process should require 100–400 kJ of work per mol of CO 2 captured and stored for relevant timescales. The process can be powered from stranded energy sources too remote to be useful for the direct needs of population centers. It may also be useful on a regional scale for protection of coral reefs from further ocean acidification. Application of this technology may involve neutralizing the alkaline solution that is coproduced with HCl with CO 2 from a point source or from the atmosphere prior to being returned to the ocean. Earth and Planetary Sciences Engineering and Applied Sciences Other/Unknown Material Carbonic acid Ocean acidification Harvard University: DASH - Digital Access to Scholarship at Harvard Environmental Science & Technology 41 24 8464 8470 |
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Open Polar |
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Harvard University: DASH - Digital Access to Scholarship at Harvard |
op_collection_id |
ftharvardudash |
language |
English |
description |
We describe an approach to CO 2 capture and storage from the atmosphere that involves enhancing the solubility of CO 2 in the ocean by a process equivalent to the natural silicate weathering reaction. HCl is electrochemically removed from the ocean and neutralized through reaction with silicate rocks. The increase in ocean alkalinity resulting from the removal of HCl causes atmospheric CO 2 to dissolve into the ocean where it will be stored primarily as HCO 3 − without further acidifying the ocean. On timescales of hundreds of years or longer, some of the additional alkalinity will likely lead to precipitation or enhanced preservation of CaCO 3 , resulting in the permanent storage of the associated carbon, and the return of an equal amount of carbon to the atmosphere. Whereas the natural silicate weathering process is effected primarily by carbonic acid, the engineered process accelerates the weathering kinetics to industrial rates by replacing this weak acid with HCl. In the thermodynamic limit—and with the appropriate silicate rocks—the overall reaction is spontaneous. A range of efficiency scenarios indicates that the process should require 100–400 kJ of work per mol of CO 2 captured and stored for relevant timescales. The process can be powered from stranded energy sources too remote to be useful for the direct needs of population centers. It may also be useful on a regional scale for protection of coral reefs from further ocean acidification. Application of this technology may involve neutralizing the alkaline solution that is coproduced with HCl with CO 2 from a point source or from the atmosphere prior to being returned to the ocean. Earth and Planetary Sciences Engineering and Applied Sciences |
author |
Aziz, Michael Schrag, Daniel House, Christopher H. House, Kurt Zenz |
spellingShingle |
Aziz, Michael Schrag, Daniel House, Christopher H. House, Kurt Zenz Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
author_facet |
Aziz, Michael Schrag, Daniel House, Christopher H. House, Kurt Zenz |
author_sort |
Aziz, Michael |
title |
Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
title_short |
Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
title_full |
Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
title_fullStr |
Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
title_full_unstemmed |
Electrochemical Acceleration of Chemical Weathering as an Energetically Feasible Approach to Mitigating Anthropogenic Climate Change |
title_sort |
electrochemical acceleration of chemical weathering as an energetically feasible approach to mitigating anthropogenic climate change |
publisher |
American Chemical Society |
publishDate |
2007 |
url |
http://nrs.harvard.edu/urn-3:HUL.InstRepos:2794947 https://doi.org/10.1021/es0701816 |
genre |
Carbonic acid Ocean acidification |
genre_facet |
Carbonic acid Ocean acidification |
op_relation |
http://dx.doi.org/10.1021/es0701816 Environmental Science and Technology House, Kurt Zenz, Christopher H. House, Daniel P. Schrag, and Michael J. Aziz. 2007. Electrochemical acceleration of chemical weathering as an energetically feasible approach to mitigating anthropogenic climate change. Environmental Science and Technology 41(24): 8464-8470. 0013-936X http://nrs.harvard.edu/urn-3:HUL.InstRepos:2794947 doi:10.1021/es0701816 |
op_doi |
https://doi.org/10.1021/es0701816 |
container_title |
Environmental Science & Technology |
container_volume |
41 |
container_issue |
24 |
container_start_page |
8464 |
op_container_end_page |
8470 |
_version_ |
1766388012849037312 |