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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Published in:Environmental Science & Technology
Main Authors: Aziz, Michael, Schrag, Daniel, House, Christopher H., House, Kurt Zenz
Language:English
Published: American Chemical Society 2007
Subjects:
Online Access:http://nrs.harvard.edu/urn-3:HUL.InstRepos:2794947
https://doi.org/10.1021/es0701816
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spelling 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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collection 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
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