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October 2008 Issue - Volume 4, Number 5

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Carbon Dioxide Sequestration

David R. Cole and Eric H. Oelkers – Guest Editors

Table of Contents

Thematic Articles

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Human and industrial development over the past hundred years has led to a huge increase in fossil fuel consumption and CO2 emissions, causing a dramatic increase in atmospheric CO2 concentration. This increased CO2 is believed to be responsible for a significant rise in global temperature over the past several decades. Global-scale climate modeling suggests that the temperature increase will continue, at least over the next few hundred years, leading to glacial melting and rising sea levels. Increased atmospheric CO2 also leads to ocean acidification, which will have drastic consequences for marine ecosystems. In an attempt to solve these problems, many have proposed the large-scale sequestration of CO2 from our atmosphere. This introductory article presents a summary of some of the evidence linking increasing atmospheric CO2 concentration to global warming and ocean acidification and our efforts to stem this rise though CO2 sequestration.
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International interest in CO2 capture and storage (CCS), as a method of reducing carbon dioxide emissions linked to global climate change, has been growing in recent years. CCS is particularly attractive for large industrial facilities, especially electric power plants, which contribute a large share of global CO2 emissions from combustion of coal and other fossil fuels. This paper describes the current status of technologies to capture CO2 and transport it to a storage site. The performance and cost of capture technologies are discussed, along with related environmental issues and the outlook for improved, lowercost strategies. The key need now is financing of full-scale demonstrations of CCS at the various types of large coal-based power plants.
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One method for minimizing climate change is to capture CO2 from power plants and inject it into the deep ocean, thus reducing the magnitude and rate of change of CO2 concentration in the atmosphere and the surface ocean. Many discharge options are possible, with varied mixing and retention characteristics. The ocean’s capacity is vast, and mathematical models suggest that injected CO2 could remain sequestered for several hundred years. While theoretical and laboratory studies support the viability of ocean storage, field experiments are necessary to realistically evaluate the environmental impact.
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Carbon dioxide capture and sequestration (CCS) in deep geological formations has recently emerged as an important option for reducing greenhouse emissions. If CCS is implemented on the scale needed to make noticeable reductions in atmospheric CO2, a billion metric tons or more must be sequestered annually—a 250 fold increase over the amount sequestered today. Securing such a large volume will require a solid scientific foundation defining the coupled hydrologic–geochemical–geomechanical processes that govern the long-term fate of CO2 in the subsurface. Also needed are methods to characterize and select sequestration sites, subsurface engineering to optimize performance and cost, approaches to ensure safe operation, monitoring technology, remediation methods, regulatory overview, and an institutional approach for managing long-term liability.
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Asurvey of the global carbon reservoirs suggests that the most stable, long-term storage mechanism for atmospheric CO2 is the formation of carbonate minerals such as calcite, dolomite and magnesite. The feasibility is demonstrated by the proportion of terrestrial carbon bound in these minerals: at least 40,000 times more carbon is present in carbonate rocks than in the atmosphere. Atmospheric carbon can be transformed into carbonate minerals either ex situ, as part of an industrial process, or in situ, by injection into geological formations where the elements required for carbonate-mineral formation are present. Many challenges in mineral carbonation remain to be resolved. They include overcoming the slow kinetics of mineral–fluid reactions, dealing with the large volume of source material required and reducing the energy needed to hasten the carbonation process. To address these challenges, several pilot studies have been launched, including the CarbFix program in Iceland. The aim of CarbFix is to inject CO2 into permeable basaltic rocks in an attempt to form carbonate minerals directly through a coupled dissolution– precipitation process.
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