An Assessment of Geological Carbon Sequestration Options in the Illinois Basin

Energy Technology Data Exchange (ETDEWEB)

Robert Finley

2005-09-30

The Midwest Geological Sequestration Consortium (MGSC) has investigated the options for geological carbon dioxide (CO{sub 2}) sequestration in the 155,400-km{sup 2} (60,000-mi{sup 2}) Illinois Basin. Within the Basin, underlying most of Illinois, western Indiana, and western Kentucky, are relatively deeper and/or thinner coal resources, numerous mature oil fields, and deep salt-water-bearing reservoirs that are potentially capable of storing CO{sub 2}. The objective of this Assessment was to determine the technical and economic feasibility of using these geological sinks for long-term storage to avoid atmospheric release of CO{sub 2} from fossil fuel combustion and thereby avoid the potential for adverse climate change. The MGSC is a consortium of the geological surveys of Illinois, Indiana, and Kentucky joined by six private corporations, five professional business associations, one interstate compact, two university researchers, two Illinois state agencies, and two consultants. The purpose of the Consortium is to assess carbon capture, transportation, and storage processes and their costs and viability in the three-state Illinois Basin region. The Illinois State Geological Survey serves as Lead Technical Contractor for the Consortium. The Illinois Basin region has annual emissions from stationary anthropogenic sources exceeding 276 million metric tonnes (304 million tons) of CO{sub 2} (>70 million tonnes (77 million tons) carbon equivalent), primarily from coal-fired electric generation facilities, some of which burn almost 4.5 million tonnes (5 million tons) of coal per year. Assessing the options for capture, transportation, and storage of the CO{sub 2} emissions within the region has been a 12-task, 2-year process that has assessed 3,600 million tonnes (3,968 million tons) of storage capacity in coal seams, 140 to 440 million tonnes (154 to 485 million tons) of capacity in mature oil reservoirs, 7,800 million tonnes (8,598 million tons) of capacity in saline

Carbon Capture and Sequestration. Potential Environmental Impacts

Energy Technology Data Exchange (ETDEWEB)

Johnston, P.; Santillo, D. [Greenpeace Research Laboratories, University of Exeter, Prince of Wales Road, Exeter, EX4 4PS (United Kingdom)

2003-02-01

Over the last few years, understanding of the profound implications of anthropogenically driven climate change has grown. In turn, this has fuelled research into options to mitigate likely impacts. Approaches involving the capture of carbon dioxide and its storage in geological formations, or in marine waters, have generated a raft of proposed solutions. The scale of some of these proposals is such that they will exert impacts of global significance in their own right. Proposals fall into two broad categories: (1) storage of liquid CO2 or products of reacted CO2 into intermediate/deep oceanic waters. and (2) storage of liquid CO2 into sub-seabed or terrestrial geological formations. For the most part, while the technical feasibility of these schemata has been widely explored, the same is not true of their ecological implications. In the case of deep/intermediate oceanic waters, poor baseline understanding of the associated ecosystems is a considerable impediment to any reliable predictive assessment of likely impacts of carbon dioxide storage in these systems. Disruption of marine microbiological processes and degradation of benthic ecosystems, including those with high levels of endemicity, have been identified as potentially serious impacts. Similarly, the physiology, ecology and likely responses of micro-organisms present in targeted geological formations require evaluation prior to any consideration of the use of such formations for storage of CO2. In addition, the impacts of any leakage to surface need also to be considered. Accordingly this paper explores current uncertainties and detailed informational needs related to ocean and geological storage of fossil fuel-derived CO2. Particular emphasis is placed upon the ecological impacts of these proposals in relation to existing and emergent understanding of deep water/soil ecosystems and the indeterminacies attached to this understanding.

A survey of the Carbon Capture

International Nuclear Information System (INIS)

Jokrllova, J.; Cik, G.; Takacova, A.; Smolinska, M.

2014-01-01

The concentration of carbon dioxide, one of the most important representatives of greenhouse gases in the atmosphere continues to rise. Fossil fuels burned in thermal power plants currently represent 80% of total energy production around the world and are the largest point sources of CO 2 , accounting for approximately 40% of total CO 2 emissions. There are several options for reducing CO 2 emissions: reducing demand, improving production efficiency and carbon capture and storage (CCS, carbon capture and storage). Capture and storage of carbon dioxide is generally a three-step process: 1 st Capture and compression of combustion products, 2 nd transport (mostly pipeline) and 3 rd utilization (eg. production of urea, beverage industry, production of dry ice, etc.). Technologies for CO 2 capturing used in power plants burning fossil fuels can be divided into four groups, each of which requires a completely different approach to CO 2 capture.

Near-term deployment of carbon capture and sequestration from biorefineries in the United States.

Science.gov (United States)

Sanchez, Daniel L; Johnson, Nils; McCoy, Sean T; Turner, Peter A; Mach, Katharine J

2018-05-08

Capture and permanent geologic sequestration of biogenic CO 2 emissions may provide critical flexibility in ambitious climate change mitigation. However, most bioenergy with carbon capture and sequestration (BECCS) technologies are technically immature or commercially unavailable. Here, we evaluate low-cost, commercially ready CO 2 capture opportunities for existing ethanol biorefineries in the United States. The analysis combines process engineering, spatial optimization, and lifecycle assessment to consider the technical, economic, and institutional feasibility of near-term carbon capture and sequestration (CCS). Our modeling framework evaluates least cost source-sink relationships and aggregation opportunities for pipeline transport, which can cost-effectively transport small CO 2 volumes to suitable sequestration sites; 216 existing US biorefineries emit 45 Mt CO 2 annually from fermentation, of which 60% could be captured and compressed for pipeline transport for under $25/tCO 2 A sequestration credit, analogous to existing CCS tax credits, of $60/tCO 2 could incent 30 Mt of sequestration and 6,900 km of pipeline infrastructure across the United States. Similarly, a carbon abatement credit, analogous to existing tradeable CO 2 credits, of $90/tCO 2 can incent 38 Mt of abatement. Aggregation of CO 2 sources enables cost-effective long-distance pipeline transport to distant sequestration sites. Financial incentives under the low-carbon fuel standard in California and recent revisions to existing federal tax credits suggest a substantial near-term opportunity to permanently sequester biogenic CO 2 This financial opportunity could catalyze the growth of carbon capture, transport, and sequestration; improve the lifecycle impacts of conventional biofuels; support development of carbon-negative fuels; and help fulfill the mandates of low-carbon fuel policies across the United States. Copyright © 2018 the Author(s). Published by PNAS.

Federal Control of Geological Carbon Sequestration

Energy Technology Data Exchange (ETDEWEB)

Reitze, Arnold W. [Univ. of Utah, Salt Lake City, UT (United States)

2011-04-01

The United States has economically recoverable coal reserves of about 261 billion tons, which is in excess of a 250-­year supply based on 2009 consumption rates. However, in the near future the use of coal may be legally restricted because of concerns over the effects of its combustion on atmospheric carbon dioxide concentrations. In response, the U.S. Department of Energy is making significant efforts to help develop and implement a commercial scale program of geologic carbon sequestration that involves capturing and storing carbon dioxide emitted from coal-burning electric power plants in deep underground formations. This article explores the technical and legal problems that must be resolved in order to have a viable carbon sequestration program. It covers the responsibilities of the United States Environmental Protection Agency and the Departments of Energy, Transportation and Interior. It discusses the use of the Safe Drinking Water Act, the Clean Air Act, the National Environmental Policy Act, the Endangered Species Act, and other applicable federal laws. Finally, it discusses the provisions related to carbon sequestration that have been included in the major bills dealing with climate change that Congress has been considering in 2009 and 2010. The article concludes that the many legal issues that exist can be resolved, but whether carbon sequestration becomes a commercial reality will depend on reducing its costs or by imposing legal requirements on fossil-fired power plants that result in the costs of carbon emissions increasing to the point that carbon sequestration becomes a feasible option.

Carbon captured from the air

International Nuclear Information System (INIS)

Keith, D.

2008-01-01

This article presented an innovative way to achieve the efficient capture of atmospheric carbon. A team of scientists from the University of Calgary's Institute for Sustainable Energy, Environment and Economy have shown that it is possible to reduce carbon dioxide (CO 2 ) using a simple machine that can capture the trace amount of CO 2 present in ambient air at any place on the planet. The thermodynamics of capturing the small concentrations of CO 2 from the air is only slightly more difficult than capturing much larger concentrations of CO 2 from power plants. The research is significant because it offers a way to capture CO 2 emissions from transportation sources such as vehicles and airplanes, which represent more than half of the greenhouse gases emitted on Earth. The energy efficient and cost effective air capture technology could complement other approaches for reducing emissions from the transportation sector, such as biofuels and electric vehicles. Air capture differs from carbon capture and storage (CCS) technology used at coal-fired power plants where CO 2 is captured and pipelined for permanent storage underground. Air capture can capture the CO 2 that is present in ambient air and store it wherever it is cheapest. The team at the University of Calgary showed that CO 2 could be captured directly from the air with less than 100 kWhrs of electricity per tonne of CO 2 . A custom-built tower was able to capture the equivalent of 20 tonnes per year of CO 2 on a single square meter of scrubbing material. The team devised a way to use a chemical process from the pulp and paper industry to cut the energy cost of air capture in half. Although the technology is only in its early stage, it appears that CO 2 could be captured from the air with an energy demand comparable to that needed for CO 2 capture from conventional power plants, but costs will be higher. The simple, reliable and scalable technology offers an opportunity to build a commercial-scale plant. 1 fig

Capacitance for carbon capture

International Nuclear Information System (INIS)

Landskron, Kai

2018-01-01

Metal recycling: A sustainable, capacitance-assisted carbon capture and sequestration method (Supercapacitive Swing Adsorption) can turn scrap metal and CO 2 into metal carbonates at an attractive energy cost. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Carbon capture by hybrid separation processes

NARCIS (Netherlands)

van Benthum, R.J.; van Kemenade, H.P.; Brouwers, J.J.H.

2014-01-01

Even though there is an increasing development of carbon capture technology over the last decade, large-scale implementation is still far from common practice, mainly caused by the energy intensiveness of carbon capture processes and the lack of regulation. In absence of strict regulation, less

Capacitance for carbon capture

Energy Technology Data Exchange (ETDEWEB)

Landskron, Kai [Department of Chemistry, Lehigh University, Bethlehem, PA (United States)

2018-03-26

Metal recycling: A sustainable, capacitance-assisted carbon capture and sequestration method (Supercapacitive Swing Adsorption) can turn scrap metal and CO{sub 2} into metal carbonates at an attractive energy cost. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Toward transformational carbon capture systems

Energy Technology Data Exchange (ETDEWEB)

Miller, David C. [National Energy Technology Laboratory, U.S. Dept. of Energy, Pittsburgh PA (United States); Litynski, John T. [Office of Fossil Energy, U.S. Dept. of Energy, Washington DC (United States); Brickett, Lynn A. [National Energy Technology Laboratory, U.S. Dept. of Energy, Pittsburgh PA (United States); Morreale, Bryan D. [National Energy Technology Laboratory, U.S. Dept. of Energy, Pittsburgh PA (United States)

2015-10-28

This paper will briefly review the history and current state of Carbon Capture and Storage (CCS) research and development and describe the technical barriers to carbon capture. it will argue forcefully for a new approach to R&D, which leverages both simulation and physical systems at the laboratory and pilot scales to more rapidly move the best technoogies forward, prune less advantageous approaches, and simultaneously develop materials and processes.

Carbon Capture: A Technology Assessment

Science.gov (United States)

2013-10-21

whereas laboratory-scale experiments typically seek to validate or obtain data for specific components of a system. Laboratory- and bench-scale processes...Plant,” Energy, vol. 35 (2010), pp. 841-850. E. Favre, R. Bounaceur, and D. Roizard, “ Biogas , Membranes and Carbon Dioxide Capture,” Journal of...pp. 1-49. 64 Favre, “ Biogas , Membranes.” Carbon Capture: A Technology Assessment Congressional Research Service 42 materials have pore sizes

Carbon captured from the air

Energy Technology Data Exchange (ETDEWEB)

Keith, D. [Calgary Univ., AB (Canada)

2008-10-15

This article presented an innovative way to achieve the efficient capture of atmospheric carbon. A team of scientists from the University of Calgary's Institute for Sustainable Energy, Environment and Economy have shown that it is possible to reduce carbon dioxide (CO{sub 2}) using a simple machine that can capture the trace amount of CO{sub 2} present in ambient air at any place on the planet. The thermodynamics of capturing the small concentrations of CO{sub 2} from the air is only slightly more difficult than capturing much larger concentrations of CO{sub 2} from power plants. The research is significant because it offers a way to capture CO{sub 2} emissions from transportation sources such as vehicles and airplanes, which represent more than half of the greenhouse gases emitted on Earth. The energy efficient and cost effective air capture technology could complement other approaches for reducing emissions from the transportation sector, such as biofuels and electric vehicles. Air capture differs from carbon capture and storage (CCS) technology used at coal-fired power plants where CO{sub 2} is captured and pipelined for permanent storage underground. Air capture can capture the CO{sub 2} that is present in ambient air and store it wherever it is cheapest. The team at the University of Calgary showed that CO{sub 2} could be captured directly from the air with less than 100 kWhrs of electricity per tonne of CO{sub 2}. A custom-built tower was able to capture the equivalent of 20 tonnes per year of CO{sub 2} on a single square meter of scrubbing material. The team devised a way to use a chemical process from the pulp and paper industry to cut the energy cost of air capture in half. Although the technology is only in its early stage, it appears that CO{sub 2} could be captured from the air with an energy demand comparable to that needed for CO{sub 2} capture from conventional power plants, but costs will be higher. The simple, reliable and scalable technology

CO2 Capture Project-An Integrated, Collaborative Technology Development Project for Next Generation CO2 Separation, Capture and Geologic Sequestration

Energy Technology Data Exchange (ETDEWEB)

Helen Kerr; Linda M. Curran

2005-04-15

The CO{sub 2} Capture Project (CCP) was a joint industry project, funded by eight energy companies (BP, ChevronTexaco, EnCana, ENI, Norsk Hydro, Shell, Statoil, and Suncor) and three government agencies (European Union [DG RES & DG TREN], the Norwegian Research Council [Klimatek Program] and the U.S. Department of Energy [NETL]). The project objective was to develop new technologies that could reduce the cost of CO{sub 2} capture and geologic storage by 50% for retrofit to existing plants and 75% for new-build plants. Technologies were to be developed to ''proof of concept'' stage by the end of 2003. Certain promising technology areas were increased in scope and the studies extended through 2004. The project budget was approximately $26.4 million over 4 years and the work program is divided into eight major activity areas: Baseline Design and Cost Estimation--defined the uncontrolled emissions from each facility and estimate the cost of abatement in $/tonne CO{sub 2}. Capture Technology, Post Combustion: technologies, which can remove CO{sub 2} from exhaust gases after combustion. Capture Technology, Oxyfuel: where oxygen is separated from the air and then burned with hydrocarbons to produce an exhaust with high CO{sub 2} for storage. Capture Technology, Pre-Combustion: in which, natural gas and petroleum cokes are converted to hydrogen and CO{sub 2} in a reformer/gasifier. Common Economic Model/Technology Screening: analysis and evaluation of each technology applied to the scenarios to provide meaningful and consistent comparison. New Technology Cost Estimation: on a consistent basis with the baseline above, to demonstrate cost reductions. Geologic Storage, Monitoring and Verification (SMV): providing assurance that CO{sub 2} can be safely stored in geologic formations over the long term. Non-Technical: project management, communication of results and a review of current policies and incentives governing CO{sub 2} capture and storage. Pre

Rates of CO2 Mineralization in Geological Carbon Storage.

Science.gov (United States)

Zhang, Shuo; DePaolo, Donald J

2017-09-19

Geologic carbon storage (GCS) involves capture and purification of CO 2 at industrial emission sources, compression into a supercritical state, and subsequent injection into geologic formations. This process reverses the flow of carbon to the atmosphere with the intention of returning the carbon to long-term geologic storage. Models suggest that most of the injected CO 2 will be "trapped" in the subsurface by physical means, but the most risk-free and permanent form of carbon storage is as carbonate minerals (Ca,Mg,Fe)CO 3 . The transformation of CO 2 to carbonate minerals requires supply of the necessary divalent cations by dissolution of silicate minerals. Available data suggest that rates of transformation are highly uncertain and difficult to predict by standard approaches. Here we show that the chemical kinetic observations and experimental results, when they can be reduced to a single cation-release time scale that describes the fractional rate at which cations are released to solution by mineral dissolution, show sufficiently systematic behavior as a function of pH, fluid flow rate, and time that the rates of mineralization can be estimated with reasonable certainty. The rate of mineralization depends on both the abundance (determined by the reservoir rock mineralogy) and the rate at which cations are released from silicate minerals by dissolution into pore fluid that has been acidified with dissolved CO 2 . Laboratory-measured rates and field observations give values spanning 8 to 10 orders of magnitude, but when they are evaluated in the context of a reservoir-scale reactive transport simulation, this range becomes much smaller. The reservoir scale simulations provide limits on the applicable conditions under which silicate mineral dissolution and subsequent carbonate mineral precipitation are likely to occur (pH 4.5 to 6, fluid flow velocity less than 5 m/year, and 50-100 years or more after the start of injection). These constraints lead to estimates of

A national look at carbon capture and storage-National carbon sequestration database and geographical information system (NatCarb)

Science.gov (United States)

Carr, T.R.; Iqbal, A.; Callaghan, N.; ,; Look, K.; Saving, S.; Nelson, K.

2009-01-01

The US Department of Energy's Regional Carbon Sequestration Partnerships (RCSPs) are responsible for generating geospatial data for the maps displayed in the Carbon Sequestration Atlas of the United States and Canada. Key geospatial data (carbon sources, potential storage sites, transportation, land use, etc.) are required for the Atlas, and for efficient implementation of carbon sequestration on a national and regional scale. The National Carbon Sequestration Database and Geographical Information System (NatCarb) is a relational database and geographic information system (GIS) that integrates carbon storage data generated and maintained by the RCSPs and various other sources. The purpose of NatCarb is to provide a national view of the carbon capture and storage potential in the U.S. and Canada. The digital spatial database allows users to estimate the amount of CO2 emitted by sources (such as power plants, refineries and other fossil-fuel-consuming industries) in relation to geologic formations that can provide safe, secure storage sites over long periods of time. The NatCarb project is working to provide all stakeholders with improved online tools for the display and analysis of CO2 carbon capture and storage data. NatCarb is organizing and enhancing the critical information about CO2 sources and developing the technology needed to access, query, model, analyze, display, and distribute natural resource data related to carbon management. Data are generated, maintained and enhanced locally at the RCSP level, or at specialized data warehouses, and assembled, accessed, and analyzed in real-time through a single geoportal. NatCarb is a functional demonstration of distributed data-management systems that cross the boundaries between institutions and geographic areas. It forms the first step toward a functioning National Carbon Cyberinfrastructure (NCCI). NatCarb provides access to first-order information to evaluate the costs, economic potential and societal issues of

Carbon capture and storage: Fundamental thermodynamics and current technology

International Nuclear Information System (INIS)

Page, S.C.; Williamson, A.G.; Mason, I.G.

2009-01-01

Carbon capture and storage (CCS) is considered a leading technology for reducing CO 2 emissions from fossil-fuelled electricity generation plants and could permit the continued use of coal and gas whilst meeting greenhouse gas targets. However considerable energy is required for the capture, compression, transport and storage steps involved. In this paper, energy penalty information in the literature is reviewed, and thermodynamically ideal and 'real world' energy penalty values are calculated. For a sub-critical pulverized coal (PC) plant, the energy penalty values for 100% capture are 48.6% and 43.5% for liquefied CO 2 , and for CO 2 compressed to 11 MPa, respectively. When assumptions for supercritical plants were incorporated, results were in broad agreement with published values arising from process modelling. However, we show that energy use in existing capture operations is considerably greater than indicated by most projections. Full CCS demonstration plants are now required to verify modelled energy penalty values. However, it appears unlikely that CCS will deliver significant CO 2 reductions in a timely fashion. In addition, many uncertainties remain over the permanence of CO 2 storage, either in geological formations, or beneath the ocean. We conclude that further investment in CCS should be seriously questioned by policy makers.

Analysis and Comparison of Carbon Capture & Sequestration Policies

Science.gov (United States)

Burton, E.; Ezzedine, S. M.; Reed, J.; Beyer, J. H.; Wagoner, J. L.

2010-12-01

Several states and countries have adopted or are in the process of crafting policies to enable geologic carbon sequestration projects. These efforts reflect the recognition that existing statutory and regulatory frameworks leave ambiguities or gaps that elevate project risk for private companies considering carbon sequestration projects, and/or are insufficient to address a government’s mandate to protect the public interest. We have compared the various approaches that United States’ state and federal governments have taken to provide regulatory frameworks to address carbon sequestration. A major purpose of our work is to inform the development of any future legislation in California, should it be deemed necessary to meet the goals of Assembly Bill 1925 (2006) to accelerate the adoption of cost-effective geologic sequestration strategies for the long-term management of industrial carbon dioxide in the state. Our analysis shows a diverse issues are covered by adopted and proposed carbon capture and sequestration (CCS) legislation and that many of the new laws focus on defining regulatory frameworks for underground injection of CO2, ambiguities in property issues, or assigning legal liability. While these approaches may enable the progress of early projects, future legislation requires a longer term and broader view that includes a quantified integration of CCS into a government’s overall climate change mitigation strategy while considering potentially counterproductive impacts on CCS of other climate change mitigation strategies. Furthermore, legislation should be crafted in the context of a vision for CCS as an economically viable and widespread industry. While an important function of new CCS legislation is enabling early projects, it must be kept in mind that applying the same laws or protocols in the future to a widespread CCS industry may result in business disincentives and compromise of the public interest in mitigating GHG emissions. Protection of the

Carbon capture and sequestration (CCS)

Science.gov (United States)

2009-06-19

Carbon capture and sequestration (or storage)known as CCShas attracted interest as a : measure for mitigating global climate change because large amounts of carbon dioxide (CO2) : emitted from fossil fuel use in the United States are potentiall...

Analysis of the technical potential for carbon capture and geological sequestration in the oil sector of Brazil; Analise do potencial tecnico do sequestro geologico de CO{sub 2} no setor petroleo no Brasil

Energy Technology Data Exchange (ETDEWEB)

Costa, Isabella Vaz Leal da

2009-02-15

This thesis focuses on the technologies related to CO{sub 2} capture and geological storage. The main objective of this study is to perform an analysis of the technical potential of geological sequestration of CO{sub 2} in the oil and gas sector in Brazil. Climate changes are directly related to emissions of greenhouse gases. Mainly, are related to increased carbon dioxide emissions due to the use of fossil fuels. To mitigate climate changes there are technologies that have the purpose of promoting the reduction of emissions of greenhouse gases such as the Geological Sequestration of CO{sub 2}. Thus, the study presents a description of the stages of the geological sequestration of CO{sub 2} and the state of the art of the technology in Brazil and worldwide. In addition, is presented the capacity for storage of the Brazilian sedimentary basins. Finally, this thesis analyzes the application of the described technologies in two stationary sources of great importance: refineries and oil and gas production fields. (author)

Economic Screening of Geologic Sequestration Options in the United States with a Carbon Management Geographic Information System

Energy Technology Data Exchange (ETDEWEB)

Dahowski, Robert T.(BATTELLE (PACIFIC NW LAB)); Dooley, James J.(BATTELLE (PACIFIC NW LAB)); Brown, Daryl R.(BATTELLE (PACIFIC NW LAB)); Stephan, Alex J.(BATTELLE (PACIFIC NW LAB)); Badie I. Morsi

2001-10-19

Developing a carbon management strategy is a formidable task for nations as well as individual companies. It is often difficult to understand what options are available, let alone determine which may be optimal. In response to the need for a better understanding of complex carbon management options, Battelle has developed a state-of-the-art Geographic Information System (GIS) model with economic screening capability focused on carbon capture and geologic sequestration opportunities in the United States. This paper describes the development of this GIS-based economic screening model and demonstrates its use for carbon management analysis.

Disordering fantasies of coal and technology: Carbon capture and storage in Australia

International Nuclear Information System (INIS)

Marshall, Jonathan Paul

2016-01-01

One of the main ways that continued use of coal is justified, and compensated for, is through fantasies of technology. This paper explores the politics of 'Carbon Capture and Storage' (CCS) technologies in Australia. These technologies involve capturing CO 2 emissions, usually to store them 'safely' underground in a process called 'geo-sequestration'. In Australia the idea of 'clean coal' has been heavily promoted, and is a major part of CO 2 emissions reduction plans, despite the technological difficulties, the lack of large scale working prototypes, the lack of coal company investment in such research, and the current difficulties in detecting leaks. This paper investigates the ways that the politics of 'clean coal' have functioned as psycho-social defence mechanisms, to prolong coal usage, assuage political discomfort and anxiety, and increase the systemic disturbance produced by coal power. - Highlights: • Clean coal and geological sequestration is part of Australian climate policy. • Governments have offered much to carbon capture and storage (CCS) projects. • Coal, and coal power, industries have been relatively uninterested. • Progress with CCS is problematic and has not lived up to expectations. • CCS defends against tackling the connection between coal and climate.

A Novel Strategy of Carbon Capture and Sequestration by rHLPD Processing

Directory of Open Access Journals (Sweden)

Richard Eric Riman

2016-01-01

Full Text Available Monoethanolamine (MEA scrubbing is an energy intensive process for Carbon Capture and Sequestration (CCS due to the regeneration of amine in stripping towers at high temperature (100-120 ºC and the subsequent pressurization of CO2 for geologic sequestration. In this paper, we introduce a novel method, reactive hydrothermal liquid phase densification (rHLPD, which is able to solidify (densify monolithic materials without using high temperature kilns. Then we integrate MEA-based CCS processing and mineral carbonation by using rHLPD technology. This integration is designated as rHLPD-Carbon Sequestration (rHLPD-CS process. Our results show that the CO2 captured in the MEA-CO2 solution was sequestered by the mineral (wollastonite CaSiO3 carbonation at a low operating temperature (60 ºC and simultaneously monolithic materials with a compressive strength of ~121 MPa were formed. This suggests that the use of rHLPD-CS technology eliminates the energy consumed for CO2-MEA stripping and CO2 compression and also sequesters CO2 to form value-added products, which have a potential to be utilized as construction and infrastructure materials. In contrast to the high energy requirements and excessive greenhouse gas emissions from conventional Portland cement manufacturing, our calculations show that the integration of rHLPD and CS technologies provides a low energy alternative to production of traditional cementitious binding materials.

An Assessment of the Commercial Availability of Carbon Dioxide Capture and Storage Technologies as of June 2009

Energy Technology Data Exchange (ETDEWEB)

Dooley, James J.; Davidson, Casie L.; Dahowski, Robert T.

2009-06-26

Currently, there is considerable confusion within parts of the carbon dioxide capture and storage (CCS) technical and regulatory communities regarding the maturity and commercial readiness of the technologies needed to capture, transport, inject, monitor and verify the efficacy of carbon dioxide (CO2) storage in deep, geologic formations. The purpose of this technical report is to address this confusion by discussing the state of CCS technological readiness in terms of existing commercial deployments of CO2 capture systems, CO2 transportation pipelines, CO2 injection systems and measurement, monitoring and verification (MMV) systems for CO2 injected into deep geologic structures. To date, CO2 has been captured from both natural gas and coal fired commercial power generating facilities, gasification facilities and other industrial processes. Transportation via pipelines and injection of CO2 into the deep subsurface are well established commercial practices with more than 35 years of industrial experience. There are also a wide variety of MMV technologies that have been employed to understand the fate of CO2 injected into the deep subsurface. The four existing end-to-end commercial CCS projects – Sleipner, Snøhvit, In Salah and Weyburn – are using a broad range of these technologies, and prove that, at a high level, geologic CO2 storage technologies are mature and capable of deploying at commercial scales. Whether wide scale deployment of CCS is currently or will soon be a cost-effective means of reducing greenhouse gas emissions is largely a function of climate policies which have yet to be enacted and the public’s willingness to incur costs to avoid dangerous anthropogenic interference with the Earth’s climate. There are significant benefits to be had by continuing to improve through research, development, and demonstration suite of existing CCS technologies. Nonetheless, it is clear that most of the core technologies required to address capture, transport

Basic Research Needs for Carbon Capture: Beyond 2020

Energy Technology Data Exchange (ETDEWEB)

Alivisatos, Paul [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Buchanan, Michelle [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2010-03-04

This report is based on a SC/FE workshop on Carbon Capture: Beyond 2020, held March 4–5, 2010, to assess the basic research needed to address the current technical bottlenecks in carbon capture processes and to identify key research priority directions that will provide the foundations for future carbon capture technologies. The problem of thermodynamically efficient and scalable carbon capture stands as one of the greatest challenges for modern energy researchers. The vast majority of US and global energy use derives from fossil fuels, the combustion of which results in the emission of carbon dioxide into the atmosphere. These anthropogenic emissions are now altering the climate. Although many alternatives to combustion are being considered, the fact is that combustion will remain a principal component of the global energy system for decades to come. Today’s carbon capture technologies are expensive and cumbersome and energy intensive. If scientists could develop practical and cost-effective methods to capture carbon, those methods would at once alter the future of the largest industry in the world and provide a technical solution to one of the most vexing problems facing humanity. The carbon capture problem is a true grand challenge for today’s scientists. Postcombustion CO2 capture requires major new developments in disciplines spanning fundamental theoretical and experimental physical chemistry, materials design and synthesis, and chemical engineering. To start with, the CO2 molecule itself is thermodynamically stable and binding to it requires a distortion of the molecule away from its linear and symmetric arrangement. This binding of the gas molecule cannot be too strong, however; the sheer quantity of CO2 that must be captured ultimately dictates that the capture medium must be recycled over and over. Hence the CO2 once bound, must be released with relatively little energy input. Further, the CO2 must be rapidly and selectively pulled out of a mixture

Policy Needs for Carbon Capture & Storage

Science.gov (United States)

Peridas, G.

2007-12-01

Climate change is one of the most pressing environmental problems of our time. The widespread consensus that exists on climate science requires deep cuts in greenhouse gas emissions, on the order of 50-80% globally from current levels. Reducing energy demand, increasing energy efficiency and sourcing our energy from renewable sources will, and should, play a key role in achieving these cuts. Fossil fuels however are abundant, relatively inexpensive, and still make up the backbone of our energy system. Phasing out fossil fuel use will be a gradual process, and is likely to take far longer than the timeframe dictated by climate science for reducing emissions. A reliable way of decarbonizing the use of fossil fuels is needed. Carbon capture and storage (CCS) has already proven to be a technology that can safely and effectively accomplish this task. The technological know-how and the underground capacity exist to store billions of tons of carbon dioxide in mature oil and gas fields, and deep saline formations. Three large international commercial projects and several other applications have proved this, but substantial barriers remain to be overcome before CCS becomes the technology of choice in all major emitting sectors. Government has a significant role to play in surmounting these barriers. Without mandatory limits on greenhouse gas emissions and a price on carbon, CCS is likely to linger in the background. The expected initial carbon price levels and their potential volatility under such a scheme dictates that further policies be used in the early years in order for CCS to be implemented. Such policies could include a new source performance standard for power plants, and a low carbon generation obligation that would relieve first movers by spreading the additional cost of the technology over entire sectors. A tax credit for capturing and permanently sequestering anthropogenic CO2 would aid project economics. Assistance in the form of loan guarantees for components

Important accounting issues for carbon dioxide capture and storage projects under the UNFCCC

International Nuclear Information System (INIS)

Haefeli, S.; Bosi, M.; Philibert, C.

2005-01-01

Carbon dioxide capture and storage (CCS) provides options for making continued use of fossil fuels more compatible with pollution abatement policies. This paper evaluated policy issues related to CCS, with particular focus on the geological sequestration of carbon dioxide (CO 2 ) into geological storage sites. Before any carbon dioxide (CO 2 ) CCS activities can be included in the portfolio of climate change mitigation activities, several issues need to be resolved such as the development of appropriate accounting and baselines rules and monitoring modalities. Guidance and policies on baselines and the accounting of emission reductions are critical to ensure that CCS projects can benefit from CO 2 markets and are recognized under various mitigation schemes. This paper examined the major issues that should considered along with changes to current accounting approaches. Issues that need to be addressed in order to prepare national inventories for the inclusion of CCS under the United Nations Framework Convention on Climate Change (UNFCCC) and emission reduction schemes such as the European greenhouse gas emissions trading scheme were first presented, followed by an examination of CCS issues under project-based mechanisms such as the Kyoto Protocol's Clean Development Mechanism. The importance of clear definitions and monitoring guidelines for the proper accounting of CCS were also highlighted. 12 refs., 2 figs

A Novel Strategy for Carbon Capture and Sequestration by rHLPD Processing

Energy Technology Data Exchange (ETDEWEB)

Li, Qinghua; Gupta, Surojit; Tang, Ling; Quinn, Sean [Department of Material Science and Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ (United States); Atakan, Vahit [Solidia Technologies, Inc., Piscataway, NJ (United States); Riman, Richard E., E-mail: riman@rci.rutgers.edu [Department of Material Science and Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ (United States)

2016-01-22

Monoethanolamine (MEA) scrubbing is an energy-intensive process for carbon capture and sequestration (CCS) due to the regeneration of amine in stripping towers at high temperature (100–120°C) and the subsequent pressurization of CO{sub 2} for geological sequestration. In this paper, we introduce a novel method, reactive hydrothermal liquid phase densification (rHLPD), which is able to solidify (densify) monolithic materials without using high temperature kilns. Then, we integrate MEA-based CCS processing and mineral carbonation by using rHLPD technology. This integration is designated as rHLPD-carbon sequestration (rHLPD-CS) process. Our results show that the CO{sub 2} captured in the MEA-CO{sub 2} solution was sequestered by the mineral (wollastonite CaSiO{sub 3}) carbonation at a low operating temperature (60°C) and simultaneously monolithic materials with a compressive strength of ~121 MPa were formed. This suggests that the use of rHLPD-CS technology eliminates the energy consumed for CO{sub 2}-MEA stripping and CO{sub 2} compression and also sequesters CO{sub 2} to form value-added products, which have a potential to be utilized as construction and infrastructure materials. In contrast to the high energy requirements and excessive greenhouse gas emissions from conventional Portland cement manufacturing, our calculations show that the integration of rHLPD and CS technologies provides a low energy alternative to production of traditional cementitious-binding materials.

Regional Opportunities for Carbon Dioxide Capture and Storage in China: A Comprehensive CO2 Storage Cost Curve and Analysis of the Potential for Large Scale Carbon Dioxide Capture and Storage in the People’s Republic of China

Energy Technology Data Exchange (ETDEWEB)

Dahowski, Robert T.; Li, Xiaochun; Davidson, Casie L.; Wei, Ning; Dooley, James J.

2009-12-01

This study presents data and analysis on the potential for carbon dioxide capture and storage (CCS) technologies to deploy within China, including a survey of the CO2 source fleet and potential geologic storage capacity. The results presented here indicate that there is significant potential for CCS technologies to deploy in China at a level sufficient to deliver deep, sustained and cost-effective emissions reductions for China over the course of this century.

CO2 Capture by Carbon Aerogel–Potassium Carbonate Nanocomposites

Directory of Open Access Journals (Sweden)

Guang Yang

2016-01-01

Full Text Available Recently, various composites for reducing CO2 emissions have been extensively studied. Because of their high sorption capacity and low cost, alkali metal carbonates are recognized as a potential candidate to capture CO2 from flue gas under moist conditions. However, undesirable effects and characteristics such as high regeneration temperatures or the formation of byproducts lead to high energy costs associated with the desorption process and impede the application of these materials. In this study, we focused on the regeneration temperature of carbon aerogel–potassium carbonate (CA–KC nanocomposites, where KC nanocrystals were formed in the mesopores of the CAs. We observed that the nanopore size of the original CA plays an important role in decreasing the regeneration temperature and in enhancing the CO2 capture capacity. In particular, 7CA–KC, which was prepared from a CA with 7 nm pores, exhibited excellent performance, reducing the desorption temperature to 380 K and exhibiting a high CO2 capture capacity of 13.0 mmol/g-K2CO3, which is higher than the theoretical value for K2CO3 under moist conditions.

Computational Modeling of the Geologic Sequestration of Carbon Dioxide

Science.gov (United States)

Geologic sequestration of CO2 is a component of C capture and storage (CCS), an emerging technology for reducing CO2 emissions to the atmosphere, and involves injection of captured CO2 into deep subsurface formations. Similar to the injection of hazardous wastes, before injection...

Computational materials chemistry for carbon capture using porous materials

International Nuclear Information System (INIS)

Sharma, Abhishek; Malani, Ateeque; Huang, Runhong; Babarao, Ravichandar

2017-01-01

Control over carbon dioxide (CO 2 ) release is extremely important to decrease its hazardous effects on the environment such as global warming, ocean acidification, etc. For CO 2 capture and storage at industrial point sources, nanoporous materials offer an energetically viable and economically feasible approach compared to chemisorption in amines. There is a growing need to design and synthesize new nanoporous materials with enhanced capability for carbon capture. Computational materials chemistry offers tools to screen and design cost-effective materials for CO 2 separation and storage, and it is less time consuming compared to trial and error experimental synthesis. It also provides a guide to synthesize new materials with better properties for real world applications. In this review, we briefly highlight the various carbon capture technologies and the need of computational materials design for carbon capture. This review discusses the commonly used computational chemistry-based simulation methods for structural characterization and prediction of thermodynamic properties of adsorbed gases in porous materials. Finally, simulation studies reported on various potential porous materials, such as zeolites, porous carbon, metal organic frameworks (MOFs) and covalent organic frameworks (COFs), for CO 2 capture are discussed. (topical review)

The thermodynamics of direct air capture of carbon dioxide

International Nuclear Information System (INIS)

Lackner, Klaus S.

2013-01-01

An analysis of thermodynamic constraints shows that the low concentration of carbon dioxide in ambient air does not pose stringent limits on air capture economics. The thermodynamic energy requirement is small even using an irreversible sorbent-based process. A comparison to flue gas scrubbing suggests that the additional energy requirement is small and can be supplied with low-cost energy. In general, the free energy expended in the regeneration of a sorbent will exceed the free energy of mixing, as absorption is usually not reversible. The irreversibility, which grows with the depth of scrubbing, tends to affect flue gas scrubbing more than air capture which can successfully operate while extracting only a small fraction of the carbon dioxide available in air. This is reflected in a significantly lower theoretical thermodynamic efficiency for a single stage flue gas scrubber than for an air capture device, but low carbon dioxide concentration in air still results in a larger energy demand for air capture. The energy required for capturing carbon dioxide from air could be delivered in various ways. I analyze a thermal swing and also a previously described moisture swing which is driven by the evaporation of water. While the total amount of heat supplied for sorbent regeneration in a thermal swing, in accordance with Carnot's principle, exceeds the total free energy requirement, the additional free energy required as one moves from flue gas scrubbing to air capture can be paid with an amount of additional low grade heat that equals the additional free energy requirement. Carnot's principle remains satisfied because the entire heat supplied, not just the additional amount, must be delivered at a slightly higher temperature. Whether the system is driven by water evaporation or by low grade heat, the cost of the thermodynamically-required energy can be as small as $1 to $2 per metric ton of carbon dioxide. Thermodynamics does not pose a practical constraint on the

Assessment of policy impacts on carbon capture and sequestration and bioenergy for U.S.' coal and natural gas power plants

Science.gov (United States)

Spokas, K.; Patrizio, P.; Leduc, S.; Mesfun, S.; Kraxner, F.

2017-12-01

Reducing electricity-sector emissions relies heavily on countries' abilities to either transition away from carbon-intensive energy generation or to sequester its resultant emissions with carbon capture and storage (CCS) technologies. The use of biomass energy technologies in conjunction with carbon capture and sequestration (BECCS) presents the opportunity for net reductions in atmospheric carbon dioxide. In this study, we investigate the limitations of several common policy mechanisms to incentivize the deployment of BECCS using the techno-economic spatial optimization model BeWhere (www.iiasa.ac.at/bewhere). We consider a set of coal and natural gas power plants in the United States (U.S.) selected using a screening process that considers capacity, boiler age, and capacity factor for electricity-generation units from the EPA 2014 eGRID database. The set makes up 470 GW of generation, and produces 8,400 PJ and 2.07 GtCO2 annually. Co-firing up to 15% for coal power plants is considered, using woody-biomass residues sourced from certified and managed U.S. forests obtained from the G4M (www.iiasa.ac.at/g4m) and GeoWiki (www.geo-wiki.org) database. Geologic storage is considered with injectivity and geomechanical limitations to ensure safe storage. Costs are minimized under two policy mechanisms: a carbon tax and geologic carbon sequestration credits, such as the Q45 credits. Results show that the carbon tax scenario incentivizes co-firing at low to medium carbon taxes, but is replaced by CCS at higher tax values. Carbon taxes do not strongly incentivize BECCS, as negative emissions associated with sequestering carbon content are not accounted as revenue. On the other hand, carbon credit scenarios result in significant CCS deployment, but lack any incentive for co-firing.

Electricity without carbon dioxide: Assessing the role of carbon capture and sequestration in United States electric markets

Science.gov (United States)

Johnson, Timothy Lawrence

2002-09-01

Stabilization of atmospheric greenhouse gas concentrations will likely require significant cuts in electric sector carbon dioxide (CO2) emissions. The ability to capture and sequester CO2 in a manner compatible with today's fossil-fuel based power generating infrastructure offers a potentially low-cost contribution to a larger climate change mitigation strategy. This thesis fills a niche between economy-wide studies of CO 2 abatement and plant-level control technology assessments by examining the contribution that carbon capture and sequestration (CCS) might make toward reducing US electric sector CO2 emissions. The assessment's thirty year perspective ensures that costs sunk in current infrastructure remain relevant and allows time for technological diffusion, but remains free of assumptions about the emergence of unidentified radical innovations. The extent to which CCS might lower CO2 mitigation costs will vary directly with the dispatch of carbon capture plants in actual power-generating systems, and will depend on both the retirement of vintage capacity and competition from abatement alternatives such as coal-to-gas fuel switching and renewable energy sources. This thesis therefore adopts a capacity planning and dispatch model to examine how the current distribution of generating units, natural gas prices, and other industry trends affect the cost of CO2 control via CCS in an actual US electric market. The analysis finds that plants with CO2 capture consistently provide significant reductions in base-load emissions at carbon prices near 100 $/tC, but do not offer an economical means of meeting peak demand unless CO2 reductions in excess of 80 percent are required. Various scenarios estimate the amount by which turn-over of the existing generating infrastructure and the severity of criteria pollutant constraints reduce mitigation costs. A look at CO2 sequestration in the seabed beneath the US Outer Continental Shelf (OCS) complements this model

Annual Report: Carbon Capture (30 September 2012)

Energy Technology Data Exchange (ETDEWEB)

Luebke, David; Morreale, Bryan; Richards, George; Syamlal, Madhava

2014-04-16

Capture of carbon dioxide (CO{sub 2}) is a critical component in reducing greenhouse gas emissions from fossil fuel-based processes. The Carbon Capture research to be performed is aimed at accelerating the development of efficient, cost-effective technologies which meet the post-combustion programmatic goal of capture of 90% of the CO{sub 2} produced from an existing coal-fired power plant with less than a 35% increase in the cost of electricity (COE), and the pre-combustion goal of 90% CO{sub 2} capture with less than a 10% increase in COE. The specific objective of this work is to develop innovative materials and approaches for the economic and efficient capture of CO{sub 2} from coal-based processes, and ultimately assess the performance of promising technologies at conditions representative of field application (i.e., slip stream evaluation). The Carbon Capture research includes seven core technical research areas: post-combustion solvents, sorbents, and membranes; pre-combustion solvents, sorbents, and membranes; and oxygen (O{sub 2}) production. The goal of each of these tasks is to develop advanced materials and processes that are able to reduce the energy penalty and cost of CO{sub 2} (or O{sub 2}) separation over conventional technologies. In the first year of development, materials will be examined by molecular modeling, and then synthesized and experimentally characterized at lab scale. In the second year, they will be tested further under ideal conditions. In the third year, they will be tested under realistic conditions. The most promising materials will be tested at the National Carbon Capture Center (NCCC) using actual flue or fuel gas. Systems analyses will be used to determine whether or not materials developed are likely to meet the Department of Energy (DOE) COE targets. Materials which perform well and appear likely to improve in performance will be licensed for further development outside of the National Energy Technology Laboratory (NETL

Realistic costs of carbon capture

Energy Technology Data Exchange (ETDEWEB)

Al Juaied, Mohammed (Harvard Univ., Cambridge, MA (US). Belfer Center for Science and International Affiaris); Whitmore, Adam (Hydrogen Energy International Ltd., Weybridge (GB))

2009-07-01

There is a growing interest in carbon capture and storage (CCS) as a means of reducing carbon dioxide (CO2) emissions. However there are substantial uncertainties about the costs of CCS. Costs for pre-combustion capture with compression (i.e. excluding costs of transport and storage and any revenue from EOR associated with storage) are examined in this discussion paper for First-of-a-Kind (FOAK) plant and for more mature technologies, or Nth-of-a-Kind plant (NOAK). For FOAK plant using solid fuels the levelised cost of electricity on a 2008 basis is approximately 10 cents/kWh higher with capture than for conventional plants (with a range of 8-12 cents/kWh). Costs of abatement are found typically to be approximately US$150/tCO2 avoided (with a range of US$120-180/tCO2 avoided). For NOAK plants the additional cost of electricity with capture is approximately 2-5 cents/kWh, with costs of the range of US$35-70/tCO2 avoided. Costs of abatement with carbon capture for other fuels and technologies are also estimated for NOAK plants. The costs of abatement are calculated with reference to conventional SCPC plant for both emissions and costs of electricity. Estimates for both FOAK and NOAK are mainly based on cost data from 2008, which was at the end of a period of sustained escalation in the costs of power generation plant and other large capital projects. There are now indications of costs falling from these levels. This may reduce the costs of abatement and costs presented here may be 'peak of the market' estimates. If general cost levels return, for example, to those prevailing in 2005 to 2006 (by which time significant cost escalation had already occurred from previous levels), then costs of capture and compression for FOAK plants are expected to be US$110/tCO2 avoided (with a range of US$90-135/tCO2 avoided). For NOAK plants costs are expected to be US$25-50/tCO2. Based on these considerations a likely representative range of costs of abatement from CCS

Mountaineer Commerical Scale Carbon Capture and Storage (CCS) Project

Energy Technology Data Exchange (ETDEWEB)

Deanna Gilliland; Matthew Usher

2011-12-31

The Final Technical documents all work performed during the award period on the Mountaineer Commercial Scale Carbon Capture & Storage project. This report presents the findings and conclusions produced as a consequence of this work. As identified in the Cooperative Agreement DE-FE0002673, AEP's objective of the Mountaineer Commercial Scale Carbon Capture and Storage (MT CCS II) project is to design, build and operate a commercial scale carbon capture and storage (CCS) system capable of treating a nominal 235 MWe slip stream of flue gas from the outlet duct of the Flue Gas Desulfurization (FGD) system at AEP's Mountaineer Power Plant (Mountaineer Plant), a 1300 MWe coal-fired generating station in New Haven, WV. The CCS system is designed to capture 90% of the CO{sub 2} from the incoming flue gas using the Alstom Chilled Ammonia Process (CAP) and compress, transport, inject and store 1.5 million tonnes per year of the captured CO{sub 2} in deep saline reservoirs. Specific Project Objectives include: (1) Achieve a minimum of 90% carbon capture efficiency during steady-state operations; (2) Demonstrate progress toward capture and storage at less than a 35% increase in cost of electricity (COE); (3) Store CO{sub 2} at a rate of 1.5 million tonnes per year in deep saline reservoirs; and (4) Demonstrate commercial technology readiness of the integrated CO{sub 2} capture and storage system.

Negative emissions in ecologic transition - Case of carbon geological storage

International Nuclear Information System (INIS)

Laude-Depezay, Audrey; Royer-Adnot, Jonathan

2015-01-01

The authors first report a bibliographical review on carbon assessment of BECCS (bio-energy and carbon capture and storage), and then propose a technological innovation which would result in an improvement of their carbon print: the CO 2 -Dissolved technology. Thus, they outline the challenges of the carbon print of fossil carbon capture and storage, discusses the specificities of BECCS (transformation of biomass into energy, carbon print of BECCS processes for the production of ethanol, of electricity, or of paper pulp). They discuss the contribution of the CO 2 -dissolved technology to the production of bio-ethanol: description of a French plant and case of supercritical carbon capture and storage, characteristics of the concept (operation, carbon print assessment)

Measurement of carbon capture efficiency and stored carbon leakage

Science.gov (United States)

Keeling, Ralph F.; Dubey, Manvendra K.

2013-01-29

Data representative of a measured carbon dioxide (CO.sub.2) concentration and of a measured oxygen (O.sub.2) concentration at a measurement location can be used to determine whether the measured carbon dioxide concentration at the measurement location is elevated relative to a baseline carbon dioxide concentration due to escape of carbon dioxide from a source associated with a carbon capture and storage process. Optionally, the data can be used to quantify a carbon dioxide concentration increase at the first location that is attributable to escape of carbon dioxide from the source and to calculate a rate of escape of carbon dioxide from the source by executing a model of gas-phase transport using at least the first carbon dioxide concentration increase. Related systems, methods, and articles of manufacture are also described.

Environmental Responses to Carbon Mitigation through Geological Storage

Energy Technology Data Exchange (ETDEWEB)

Cunningham, Alfred [Montana State Univ., Bozeman, MT (United States); Bromenshenk, Jerry [Montana State Univ., Bozeman, MT (United States)

2013-08-30

In summary, this DOE EPSCoR project is contributing to the study of carbon mitigation through geological storage. Both deep and shallow subsurface research needs are being addressed through research directed at improved understanding of environmental responses associated with large scale injection of CO₂ into geologic formations. The research plan has two interrelated research objectives. Objective 1: Determine the influence of CO₂-related injection of fluids on pore structure, material properties, and microbial activity in rock cores from potential geological carbon sequestration sites. Objective 2: Determine the Effects of CO₂ leakage on shallow subsurface ecosystems (microbial and plant) using field experiments from an outdoor field testing facility.

Carbon Capture Methods and Relative Competitiveness of Primary Energies

International Nuclear Information System (INIS)

Amigues, Jean-Pierre; Lafforgue, Gilles; Moreaux, Michel

2016-01-01

We characterise the optimal exploitation paths of two primary energies (coal and solar) that supply the energy needs of two sectors. Sector 1 can reduce its carbon emissions at a reasonable cost thanks to a CCS device. Sector 2 has access only to air capture technology, but at a significantly higher cost. We assume that the atmospheric carbon stock cannot exceed a given ceiling. We show that the optimal approach consists in, first, fully capturing sector-1 emissions before the ceiling is reached and, second, deploying air capture to partially abate sector-2 emissions. The optimal carbon tax should increase in the pre-ceiling phase then decline in stages to zero

Technology Roadmap: Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2013-08-01

As long as fossil fuels and carbon-intensive industries play dominant roles in our economies, carbon capture and storage (CCS) will remain a critical greenhouse gas reduction solution. This CCS roadmap aims at assisting governments and industry in integrating CCS in their emissions reduction strategies and in creating the conditions for scaled-up deployment of all three components of the CCS chain: CO2 capture, transport and storage. To get us onto the right pathway, this roadmap highlights seven key actions needed in the next seven years to create a solid foundation for deployment of CCS starting by 2020. IEA analysis shows that CCS is an integral part of any lowest-cost mitigation scenario where long-term global average temperature increases are limited to significantly less than 4 °C, particularly for 2 °C scenarios (2DS). In the 2DS, CCS is widely deployed in both power generation and industrial applications. The total CO2 capture and storage rate must grow from the tens of megatonnes of CO2 captured in 2013 to thousands of megatonnes of CO2 in 2050 in order to address the emissions reduction challenge. A total cumulative mass of approximately 120 GtCO2 would need to be captured and stored between 2015 and 2050, across all regions of the globe.

Field Testing of Cryogenic Carbon Capture

Energy Technology Data Exchange (ETDEWEB)

Sayre, Aaron [Sustainable Energy Solutions, LLC; Frankman, Dave [Sustainable Energy Solutions, LLC; Baxter, Andrew [Sustainable Energy Solutions, LLC; Stitt, Kyler [Sustainable Energy Solutions, LLC; Baxter, Larry [Sustainable Energy Solutions, LLC; Brigham Young Univ., Provo, UT (United States)

2017-07-17

Sustainable Energy Solutions has been developing Cryogenic Carbon Capture™ (CCC) since 2008. In that time two processes have been developed, the External Cooling Loop and Compressed Flue Gas Cryogenic Carbon Capture processes (CCC ECL™ and CCC CFG™ respectively). The CCC ECL™ process has been scaled up to a 1TPD CO2 system. In this process the flue gas is cooled by an external refrigerant loop. SES has tested CCC ECL™ on real flue gas slip streams from subbituminous coal, bituminous coal, biomass, natural gas, shredded tires, and municipal waste fuels at field sites that include utility power stations, heating plants, cement kilns, and pilot-scale research reactors. The CO2 concentrations from these tests ranged from 5 to 22% on a dry basis. CO2 capture ranged from 95-99+% during these tests. Several other condensable species were also captured including NO2, SO2 and PMxx at 95+%. NO was also captured at a modest rate. The CCC CFG™ process has been scaled up to a .25 ton per day system. This system has been tested on real flue gas streams including subbituminous coal, bituminous coal and natural gas at field sites that include utility power stations, heating plants, and pilot-scale research reactors. CO2 concentrations for these tests ranged from 5 to 15% on a dry basis. CO2 capture ranged from 95-99+% during these tests. Several other condensable species were also captured including NO2, SO2 and PMxx at 95+%. NO was also captured at 90+%. Hg capture was also verified and the resulting effluent from CCC CFG™ was below a 1ppt concentration. This paper will focus on discussion of the capabilities of CCC, the results of field testing and the future steps surrounding the development of this technology.

Simulation of CO2–water–rock interactions on geologic CO2 sequestration under geological conditions of China

International Nuclear Information System (INIS)

Wang, Tianye; Wang, Huaiyuan; Zhang, Fengjun; Xu, Tianfu

2013-01-01

Highlights: • We determined the feasibilities of geologic CO 2 sequestration in China. • We determined the formation of gibbsite suggested CO 2 can be captured by rocks. • We suggested the mechanisms of CO 2 –water–rock interactions. • We found the corrosion and dissolution of the rock increased as temperature rose. -- Abstract: The main purpose of this study focused on the feasibility of geologic CO 2 sequestration within the actual geological conditions of the first Carbon Capture and Storage (CCS) project in China. This study investigated CO 2 –water–rock interactions under simulated hydrothermal conditions via physicochemical analyses and scanning electron microscopy (SEM). Mass loss measurement and SEM showed that corrosion of feldspars, silica, and clay minerals increased with increasing temperature. Corrosion of sandstone samples in the CO 2 -containing fluid showed a positive correlation with temperature. During reaction at 70 °C, 85 °C, and 100 °C, gibbsite (an intermediate mineral product) formed on the sample surface. This demonstrated mineral capture of CO 2 and supported the feasibility of geologic CO 2 sequestration. Chemical analyses suggested a dissolution–reprecipitation mechanism underlying the CO 2 –water–rock interactions. The results of this study suggested that mineral dissolution, new mineral precipitation, and carbonic acid formation-dissociation are closely interrelated in CO 2 –water–rock interactions

Multiphase, multicomponent simulations and experiments of reactive flow, relevant for combining geologic CO2 sequestration with geothermal energy capture

Science.gov (United States)

Saar, Martin O.

2011-11-01

Understanding the fluid dynamics of supercritical carbon dioxide (CO2) in brine- filled porous media is important for predictions of CO2 flow and brine displacement during geologic CO2 sequestration and during geothermal energy capture using sequestered CO2 as the subsurface heat extraction fluid. We investigate multiphase fluid flow in porous media employing particle image velocimetry experiments and lattice-Boltzmann fluid flow simulations at the pore scale. In particular, we are interested in the motion of a drop (representing a CO2 bubble) through an orifice in a plate, representing a simplified porous medium. In addition, we study single-phase/multicomponent reactive transport experimentally by injecting water with dissolved CO2 into rocks/sediments typically considered for CO2 sequestration to investigate how resultant fluid-mineral reactions modify permeability fields. Finally, we investigate numerically subsurface CO2 and heat transport at the geologic formation scale.

An Overview of Geologic Carbon Sequestration Potential in California

Energy Technology Data Exchange (ETDEWEB)

Cameron Downey; John Clinkenbeard

2005-10-01

As part of the West Coast Regional Carbon Sequestration Partnership (WESTCARB), the California Geological Survey (CGS) conducted an assessment of geologic carbon sequestration potential in California. An inventory of sedimentary basins was screened for preliminary suitability for carbon sequestration. Criteria included porous and permeable strata, seals, and depth sufficient for critical state carbon dioxide (CO{sub 2}) injection. Of 104 basins inventoried, 27 met the criteria for further assessment. Petrophysical and fluid data from oil and gas reservoirs was used to characterize both saline aquifers and hydrocarbon reservoirs. Where available, well log or geophysical information was used to prepare basin-wide maps showing depth-to-basement and gross sand distribution. California's Cenozoic marine basins were determined to possess the most potential for geologic sequestration. These basins contain thick sedimentary sections, multiple saline aquifers and oil and gas reservoirs, widespread shale seals, and significant petrophysical data from oil and gas operations. Potential sequestration areas include the San Joaquin, Sacramento, Ventura, Los Angeles, and Eel River basins, followed by the smaller Salinas, La Honda, Cuyama, Livermore, Orinda, and Sonoma marine basins. California's terrestrial basins are generally too shallow for carbon sequestration. However, the Salton Trough and several smaller basins may offer opportunities for localized carbon sequestration.

Carbon Capture and Sequestration from a Hydrogen Production Facility in an Oil Refinery

Energy Technology Data Exchange (ETDEWEB)

Engels, Cheryl; Williams, Bryan, Valluri, Kiranmal; Watwe, Ramchandra; Kumar, Ravi; Mehlman, Stewart

2010-06-21

The project proposed a commercial demonstration of advanced technologies that would capture and sequester CO2 emissions from an existing hydrogen production facility in an oil refinery into underground formations in combination with Enhanced Oil Recovery (EOR). The project is led by Praxair, Inc., with other project participants: BP Products North America Inc., Denbury Onshore, LLC (Denbury), and Gulf Coast Carbon Center (GCCC) at the Bureau of Economic Geology of The University of Texas at Austin. The project is located at the BP Refinery at Texas City, Texas. Praxair owns and operates a large hydrogen production facility within the refinery. As part of the project, Praxair would construct a CO2 capture and compression facility. The project aimed at demonstrating a novel vacuum pressure swing adsorption (VPSA) based technology to remove CO2 from the Steam Methane Reformers (SMR) process gas. The captured CO2 would be purified using refrigerated partial condensation separation (i.e., cold box). Denbury would purchase the CO2 from the project and inject the CO2 as part of its independent commercial EOR projects. The Gulf Coast Carbon Center at the Bureau of Economic Geology, a unit of University of Texas at Austin, would manage the research monitoring, verification and accounting (MVA) project for the sequestered CO2, in conjunction with Denbury. The sequestration and associated MVA activities would be carried out in the Hastings field at Brazoria County, TX. The project would exceed DOE?s target of capturing one million tons of CO2 per year (MTPY) by 2015. Phase 1 of the project (Project Definition) is being completed. The key objective of Phase 1 is to define the project in sufficient detail to enable an economic decision with regard to proceeding with Phase 2. This topical report summarizes the administrative, programmatic and technical accomplishments completed in Phase 1 of the project. It describes the work relative to project technical and design activities

Wyoming Carbon Capture and Storage Institute

Energy Technology Data Exchange (ETDEWEB)

Nealon, Teresa

2014-06-30

This report outlines the accomplishments of the Wyoming Carbon Capture and Storage (CCS) Technology Institute (WCTI), including creating a website and online course catalog, sponsoring technology transfer workshops, reaching out to interested parties via news briefs and engaging in marketing activities, i.e., advertising and participating in tradeshows. We conclude that the success of WCTI was hampered by the lack of a market. Because there were no supporting financial incentives to store carbon, the private sector had no reason to incur the extra expense of training their staff to implement carbon storage. ii

New carbon-carbon linked amphiphilic carboranyl-porphyrins as boron neutron capture agents

International Nuclear Information System (INIS)

Vicente, M.G.H.; Wickramasinghe, A.; Shetty, S.J.; Smith, K.M.

2000-01-01

Novel amphiphilic carboranyl-porphyrins have been synthesized for Boron Neutron Capture Therapy (BNCT). These compounds have carbon-carbon bonds between the carborane residues and the porphyrin meso-phenyl groups, and contain 28-31% boron by weight . (author)

Capture and geological storage of CO{sub 2}. Innovation, industrial stakes and realizations; Captage et stockage geologique du CO{sub 2}. Innovation, enjeux industriels et realisations

Energy Technology Data Exchange (ETDEWEB)

Lavergne, R.; Podkanski, J.; Rohner, H.; Otter, N.; Swift, J.; Dance, T.; Vesseron, Ph.; Reich, J.P.; Reynen, B.; Wright, L.; Marliave, L. de; Stromberg, L.; Aimard, N.; Wendel, H.; Erdol, E.; Dino, R.; Renzenbrink, W.; Birat, J.P.; Czernichowski-Lauriol, I.; Christensen, N.P.; Le Thiez, P.; Paelinck, Ph.; David, M.; Pappalardo, M.; Moisan, F.; Marston, Ph.; Law, M.; Zakkour, P.; Singer, St.; Philippe, Th.; Philippe, Th

2007-07-01

-making industries and their CO{sub 2} capture and storage needs: the ULCOS program; CO{sub 2} capture technologies: road-maps and potential cost abatement; membranes: oxygen production and hydrogen separation; CO2GeoNet: integration of European research for the establishment of confidence in CO{sub 2} geologic storage; CO2SINK, CO{sub 2} geologic storage test at the European pilot site of Ketzin (Germany); storage in aquifers for European industrial projects: AQUA CO2; the US approach: US standards for the qualification of a CO{sub 2} storage in agreement with federal and state regulations; legal and regulatory aspects; societal acceptation; CO{sub 2} capture, geologic storage and carbon market; economic aspects of CO{sub 2} capture and storage; an experience of implementation of 'clean development mechanisms' in an industrial strategy; closing talk. (J.S.)

Capture and geological storage of CO{sub 2}. Innovation, industrial stakes and realizations; Captage et stockage geologique du CO{sub 2}. Innovation, enjeux industriels et realisations

Energy Technology Data Exchange (ETDEWEB)

Lavergne, R; Podkanski, J; Rohner, H; Otter, N; Swift, J; Dance, T; Vesseron, Ph; Reich, J P; Reynen, B; Wright, L; Marliave, L de; Stromberg, L; Aimard, N; Wendel, H; Erdol, E; Dino, R; Renzenbrink, W; Birat, J P; Czernichowski-Lauriol, I; Christensen, N P; Le Thiez, P; Paelinck, Ph; David, M; Pappalardo, M; Moisan, F; Marston, Ph; Law, M; Zakkour, P; Singer, St; Philippe, Th; Philippe, Th

2007-07-01

and their CO{sub 2} capture and storage needs: the ULCOS program; CO{sub 2} capture technologies: road-maps and potential cost abatement; membranes: oxygen production and hydrogen separation; CO2GeoNet: integration of European research for the establishment of confidence in CO{sub 2} geologic storage; CO2SINK, CO{sub 2} geologic storage test at the European pilot site of Ketzin (Germany); storage in aquifers for European industrial projects: AQUA CO2; the US approach: US standards for the qualification of a CO{sub 2} storage in agreement with federal and state regulations; legal and regulatory aspects; societal acceptation; CO{sub 2} capture, geologic storage and carbon market; economic aspects of CO{sub 2} capture and storage; an experience of implementation of 'clean development mechanisms' in an industrial strategy; closing talk. (J.S.)

Operating considerations of ultrafiltration in enzyme enhanced carbon capture

DEFF Research Database (Denmark)

Deslauriers, Maria Gundersen; Gladis, Arne; Fosbøl, Philip Loldrup

2017-01-01

capture capacity of 1 MTonn CO2/year, and is here operated for one year continuously. This publication compares soluble enzymes dissolved in a capture solvent with and without the use of ultrafiltration membranes. The membranes used here have an enzyme retention of 90%, 99% and 99.9%. Enzyme retention......Today, enzyme enhanced carbon capture and storage (CCS) is gaining interest, since it can enable the use of energy efficient solvents, and thus potentially reduce the carbon footprint of CCS. However, a limitation of this technology is the high temperatures encountered in the stripper column, which...

Advanced modeling to accelerate the scale up of carbon capture technologies

Energy Technology Data Exchange (ETDEWEB)

Miller, David C.; Sun, XIN; Storlie, Curtis B.; Bhattacharyya, Debangsu

2015-06-01

In order to help meet the goals of the DOE carbon capture program, the Carbon Capture Simulation Initiative (CCSI) was launched in early 2011 to develop, demonstrate, and deploy advanced computational tools and validated multi-scale models to reduce the time required to develop and scale-up new carbon capture technologies. This article focuses on essential elements related to the development and validation of multi-scale models in order to help minimize risk and maximize learning as new technologies progress from pilot to demonstration scale.

75 FR 75059 - Mandatory Reporting of Greenhouse Gases: Injection and Geologic Sequestration of Carbon Dioxide

Science.gov (United States)

2010-12-01

... Greenhouse Gases: Injection and Geologic Sequestration of Carbon Dioxide; Final Rule #0;#0;Federal Register... Mandatory Reporting of Greenhouse Gases: Injection and Geologic Sequestration of Carbon Dioxide AGENCY... greenhouse gas monitoring and reporting from facilities that conduct geologic sequestration of carbon dioxide...

Impacts of carbon capture on power plant emissions

Energy Technology Data Exchange (ETDEWEB)

Narula, R.; Wen, H. [Bechtel Power, San Francisco, CA (United States)

2009-07-01

Post-combustion carbon dioxide capture processes currently include amine-based solvent scrubbing and ammonia solution scrubbing technologies. Both result in high emissions of volatile organic compounds (VOC) and ammonia, as well as liquid discharge that contain chemical solvent. Additional solid wastes include sludge and spent solvent filtration medias. Process simulation software can be used to predict the amount of solvent vapor in the stack gas for both amine and ammonia solvent based capture processes. However, amine could decompose in most amine-based processes and release ammonia gas due to degradation by exposure to oxygen, sulfur impurities, and thermal conditions. As a regulated pollutant for emission control for some plants, ammonia emissions are a major concern for ammonia scrubbing processes. The energy requirement for carbon capture can be reduced by cooling the flue gas before entering the carbon dioxide absorber column. The resulting low flue gas temperature could create difficulties in dispersing the flue gas plume in the atmosphere. This paper presented a computer simulation of stack emission reduction.

European CO2 prices and carbon capture investments

International Nuclear Information System (INIS)

Abadie, Luis M.; Chamorro, Jose M.

2008-01-01

We assess the option to install a carbon capture and storage (CCS) unit in a coal-fired power plant operating in a carbon-constrained environment. We consider two sources of risk, namely the price of emission allowance and the price of the electricity output. First we analyse the performance of the EU market for CO 2 emission allowances. Specifically, we focus on the contracts maturing in the Kyoto Protocol's first commitment period (2008 to 2012) and calibrate the underlying parameters of the allowance price process. Then we refer to the Spanish wholesale electricity market and calibrate the parameters of the electricity price process. We use a two-dimensional binomial lattice to derive the optimal investment rule. In particular, we obtain the trigger allowance prices above which it is optimal to install the capture unit immediately. We further analyse the effect of changes in several variables on these critical prices, among them allowance price volatility and a hypothetical government subsidy. We conclude that, at current permit prices, immediate installation does not seem justified from a financial point of view. This need not be the case, though, if carbon market parameters change dramatically, carbon capture technology undergoes significant improvements, and/or a specific governmental policy to promote these units is adopted. (author)

Carbon Dioxide Capture by Deep Eutectic Solvent Impregnated Sea Mango Activated Carbon

Science.gov (United States)

Zulkurnai, N. Z.; Ali, U. F. Md.; Ibrahim, N.; Manan, N. S. Abdul

2018-03-01

The increment amount of the CO2 emission by years has become a major concern worldwide due to the global warming issue. However, the influence modification of activated carbon (AC) has given a huge revolution in CO2 adsorption capture compare to the unmodified AC. In the present study, the Deep Eutectic Solvent (DES) modified surface AC was used for Carbon Dioxide (CO2) capture in the fixed-bed column. The AC underwent pre-carbonization and carbonization processes at 519.8 °C, respectively, with flowing of CO2 gas and then followed by impregnation with 53.75% phosphoric acid (H3PO4) at 1:2 precursor-to-activant ratios. The prepared AC known as sea mango activated carbon (SMAC) was impregnated with DES at 1:2 solid-to-liquid ratio. The DES is composing of choline chloride and urea with ratio 1:2 choline chloride to urea. The optimum adsorption capacity of SMAC was 33.46 mgco2/gsol and 39.40 mgco2/gsol for DES modified AC (DESAC).

Geological Sequestration Training and Research Program in Capture and Transport: Development of the Most Economical Separation Method for CO2 Capture

Energy Technology Data Exchange (ETDEWEB)

Vahdat, Nader

2013-09-30

The project provided hands-on training and networking opportunities to undergraduate students in the area of carbon dioxide (CO2) capture and transport, through fundamental research study focused on advanced separation methods that can be applied to the capture of CO2 resulting from the combustion of fossil-fuels for power generation . The project team’s approach to achieve its objectives was to leverage existing Carbon Capture and Storage (CCS) course materials and teaching methods to create and implement an annual CCS short course for the Tuskegee University community; conduct a survey of CO2 separation and capture methods; utilize data to verify and develop computer models for CO2 capture and build CCS networks and hands-on training experiences. The objectives accomplished as a result of this project were: (1) A comprehensive survey of CO2 capture methods was conducted and mathematical models were developed to compare the potential economics of the different methods based on the total cost per year per unit of CO2 avoidance; and (2) Training was provided to introduce the latest CO2 capture technologies and deployment issues to the university community.

Microbial and Chemical Enhancement of In-Situ Carbon Mineralization in Geological Formation

Energy Technology Data Exchange (ETDEWEB)

Matter, J.; Chandran, K.

2013-05-31

Predictions of global energy usage suggest a continued increase in carbon emissions and rising concentrations of CO{sub 2} in the atmosphere unless major changes are made to the way energy is produced and used. Various carbon capture and storage (CCS) technologies are currently being developed, but unfortunately little is known regarding the fundamental characteristics of CO{sub 2}-mineral reactions to allow a viable in-situ carbon mineralization that would provide the most permanent and safe storage of geologically-injected CO{sub 2}. The ultimate goal of this research project was to develop a microbial and chemical enhancement scheme for in-situ carbon mineralization in geologic formations in order to achieve long-term stability of injected CO{sub 2}. Thermodynamic and kinetic studies of CO{sub 2}-mineral-brine systems were systematically performed to develop the in-situ mineral carbonation process that utilizes organic acids produced by a microbial reactor. The major participants in the project are three faculty members and their graduate and undergraduate students at the School of Engineering and Applied Science and at the Lamont-Doherty Earth Observatory at Columbia University: Alissa Park in Earth and Environmental Engineering & Chemical Engineering (PI), Juerg Matter in Earth and Environmental Science (Co-PI), and Kartik Chandran in Earth and Environmental Engineering (Co-PI). Two graduate students, Huangjing Zhao and Edris Taher, were trained as a part of this project as well as a number of graduate students and undergraduate students who participated part-time. Edris Taher received his MS degree in 2012 and Huangjing Zhao will defend his PhD on Jan. 15th, 2014. The interdisciplinary training provided by this project was valuable to those students who are entering into the workforce in the United States. Furthermore, the findings from this study were and will be published in referred journals to disseminate the results. The list of the papers is given at

Tracking Progress in Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2012-09-06

At the second Clean Energy Ministerial in Abu Dhabi, April 2011 (CEM 2), the Carbon Capture, Use and Storage Action Group (CCUS AG) presented seven substantive recommendations to Energy Ministers on concrete, near-term actions to accelerate global carbon capture and storage (CCS) deployment. Twelve CCUS AG governments agreed to advance progress against the 2011 recommendations by the third Clean Energy Ministerial (London, 25-26 April 2012) (CEM 3). Following CEM 2, the CCUS AG requested the IEA and the Global CCS Institute to report on progress made against the 2011 recommendations at CEM 3. Tracking Progress in Carbon Capture and Storage: International Energy Agency/Global CCS Institute report to the third Clean Energy Ministerial responds to that request. The report considers a number of key questions. Taken as a whole, what advancements have committed CCUS AG governments made against the 2011 recommendations since CEM 2? How can Energy Ministers continue to drive progress to enable CCS to fully contribute to climate change mitigation? While urgent further action is required in all areas, are there particular areas that are currently receiving less policy attention than others, where efforts could be redoubled? The report concludes that, despite developments in some areas, significant further work is required. CCS financing and industrial applications continue to represent a particularly serious challenge.

[Carbon capture and storage (CCS) and its potential role to mitigate carbon emission in China].

Science.gov (United States)

Chen, Wen-Ying; Wu, Zong-Xin; Wang, Wei-Zhong

2007-06-01

Carbon capture and storage (CCS) has been widely recognized as one of the options to mitigate carbon emission to eventually stabilize carbon dioxide concentration in the atmosphere. Three parts of CCS, which are carbon capture, transport, and storage are assessed in this paper, covering comparisons of techno-economic parameters for different carbon capture technologies, comparisons of storage mechanism, capacity and cost for various storage formations, and etc. In addition, the role of CCS to mitigate global carbon emission is introduced. Finally, China MARKAL model is updated to include various CCS technologies, especially indirect coal liquefaction and poly-generation technologies with CCS, in order to consider carbon emission reduction as well as energy security issue. The model is used to generate different scenarios to study potential role of CCS to mitigate carbon emissions by 2050 in China. It is concluded that application of CCS can decrease marginal abatement cost and the decrease rate can reach 45% for the emission reduction rate of 50%, and it can lessen the dependence on nuclear power development for stringent carbon constrains. Moreover, coal resources can be cleanly used for longer time with CCS, e.g., for the scenario C70, coal share in the primary energy consumption by 2050 will increase from 10% when without CCS to 30% when with CCS. Therefore, China should pay attention to CCS R&D activities and to developing demonstration projects.

Multi-scale modeling of carbon capture systems

Energy Technology Data Exchange (ETDEWEB)

Kress, Joel David [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2017-03-03

The development and scale up of cost effective carbon capture processes is of paramount importance to enable the widespread deployment of these technologies to significantly reduce greenhouse gas emissions. The U.S. Department of Energy initiated the Carbon Capture Simulation Initiative (CCSI) in 2011 with the goal of developing a computational toolset that would enable industry to more effectively identify, design, scale up, operate, and optimize promising concepts. The first half of the presentation will introduce the CCSI Toolset consisting of basic data submodels, steady-state and dynamic process models, process optimization and uncertainty quantification tools, an advanced dynamic process control framework, and high-resolution filtered computationalfluid- dynamics (CFD) submodels. The second half of the presentation will describe a high-fidelity model of a mesoporous silica supported, polyethylenimine (PEI)-impregnated solid sorbent for CO₂ capture. The sorbent model includes a detailed treatment of transport and amine-CO₂- H₂O interactions based on quantum chemistry calculations. Using a Bayesian approach for uncertainty quantification, we calibrate the sorbent model to Thermogravimetric (TGA) data.

CAPTURING EXHAUST CO2 GAS USING MOLTEN CARBONATE FUEL CELLS

Directory of Open Access Journals (Sweden)

Prateek Dhawan

2016-03-01

Full Text Available Carbon dioxide is considered as one of the major contenders when the question of greenhouse effect arises. So for any industry or power plant it is of utmost importance to follow certain increasingly stringent environment protection rules and laws. So it is significant to keep eye on any possible methods to reduce carbon dioxide emissions in an efficient way. This paper reviews the available literature so as to try to provide an insight of the possibility of using Molten Carbonate Fuel Cells (MCFCs as the carbon capturing and segregating devices and the various factors that affect the performance of MCFCs during the process of CO2 capture.

Separation and capture of CO2 from large stationary sources and sequestration in geological formations--coalbeds and deep saline aquifers.

Science.gov (United States)

White, Curt M; Strazisar, Brian R; Granite, Evan J; Hoffman, James S; Pennline, Henry W

2003-06-01

The topic of global warming as a result of increased atmospheric CO2 concentration is arguably the most important environmental issue that the world faces today. It is a global problem that will need to be solved on a global level. The link between anthropogenic emissions of CO2 with increased atmospheric CO2 levels and, in turn, with increased global temperatures has been well established and accepted by the world. International organizations such as the United Nations Framework Convention on Climate Change (UNFCCC) and the Intergovernmental Panel on Climate Change (IPCC) have been formed to address this issue. Three options are being explored to stabilize atmospheric levels of greenhouse gases (GHGs) and global temperatures without severely and negatively impacting standard of living: (1) increasing energy efficiency, (2) switching to less carbon-intensive sources of energy, and (3) carbon sequestration. To be successful, all three options must be used in concert. The third option is the subject of this review. Specifically, this review will cover the capture and geologic sequestration of CO2 generated from large point sources, namely fossil-fuel-fired power gasification plants. Sequestration of CO2 in geological formations is necessary to meet the President's Global Climate Change Initiative target of an 18% reduction in GHG intensity by 2012. Further, the best strategy to stabilize the atmospheric concentration of CO2 results from a multifaceted approach where sequestration of CO2 into geological formations is combined with increased efficiency in electric power generation and utilization, increased conservation, increased use of lower carbon-intensity fuels, and increased use of nuclear energy and renewables. This review covers the separation and capture of CO2 from both flue gas and fuel gas using wet scrubbing technologies, dry regenerable sorbents, membranes, cryogenics, pressure and temperature swing adsorption, and other advanced concepts. Existing

Carbon fibre composite for ventilation air methane (VAM) capture

International Nuclear Information System (INIS)

Thiruvenkatachari, Ramesh; Su Shi; Yu Xinxiang

2009-01-01

Coal mine methane (CMM) is not only a hazardous greenhouse gas but is also a wasted energy resource, if not utilised. This paper evaluates a novel adsorbent material developed for capturing methane from ventilation air methane (VAM) gas in underground coal mines. The adsorbent material is a honeycomb monolithic carbon fibre composite (HMCFC) consisting of multiple parallel flow-through channels and the material exhibits unique features including low pressure drop, good mechanical properties, ability to handle dust-containing gas streams, good thermal and electrical conductivity and selective adsorption of gases. During this study, a series of HMCFC adsorbents (using different types of carbon fibres) were successfully fabricated. Experimental data demonstrated the proof-of-concept of using the HMCFC adsorbent to capture methane from VAM gas. The adsorption capacity of the HMCFC adsorbent was twice that of commercial activated carbon. Methane concentration of 0.56% in the inlet VAM gas stream is reduced to about 0.011% after it passes through the novel carbon fibre composite adsorbent material at ambient temperature and atmospheric pressure. This amounts to a maximum capture efficiency of 98%. These encouraging laboratory scale studies have prompted further large scale trials and economic assessment.

A scalable infrastructure model for carbon capture and storage: SimCCS

International Nuclear Information System (INIS)

Middleton, Richard S.; Bielicki, Jeffrey M.

2009-01-01

In the carbon capture and storage (CCS) process, CO 2 sources and geologic reservoirs may be widely spatially dispersed and need to be connected through a dedicated CO 2 pipeline network. We introduce a scalable infrastructure model for CCS (simCCS) that generates a fully integrated, cost-minimizing CCS system. SimCCS determines where and how much CO 2 to capture and store, and where to build and connect pipelines of different sizes, in order to minimize the combined annualized costs of sequestering a given amount of CO 2 . SimCCS is able to aggregate CO 2 flows between sources and reservoirs into trunk pipelines that take advantage of economies of scale. Pipeline construction costs take into account factors including topography and social impacts. SimCCS can be used to calculate the scale of CCS deployment (local, regional, national). SimCCS' deployment of a realistic, capacitated pipeline network is a major advancement for planning CCS infrastructure. We demonstrate simCCS using a set of 37 CO 2 sources and 14 reservoirs for California. The results highlight the importance of systematic planning for CCS infrastructure by examining the sensitivity of CCS infrastructure, as optimized by simCCS, to varying CO 2 targets. We finish by identifying critical future research areas for CCS infrastructure

Membrane Systems Engineering for Post-combustion Carbon Capture

KAUST Repository

Alshehri, Ali; Khalilpour, Rajab; Abbas, Ali; Lai, Zhiping

2013-01-01

This study proposes a strategy for optimal design of hollow fiber membrane networks for post combustion carbon capture from power plant multicomponent flue gas. A mathematical model describing multicomponent gas permeation through a separation membrane was customized into the flowsheet modeling package ASPEN PLUS. An N-stage membrane network superstructure was defined considering all possible flowsheeting configurations. An optimization formulation was then developed and solved using an objective function that minimizes the costs associated with operating and capital expenses. For a case study of flue gas feed flow rate of 298 m3/s with 13% CO2 and under defined economic parameters, the optimization resulted in the synthesis of a membrane network structure consisting of two stages in series. This optimal design was found while also considering feed and permeate pressures as well as recycle ratios between stages. The cost of carbon capture for this optimal membrane network is estimated to be $28 per tonne of CO2 captured, considering a membrane permeance of 1000 GPU and membrane selectivity of 50. Following this approach, a reduction in capture cost to less than $20 per tonne CO2 captured is possible if membranes with permeance of 2000 GPU and selectivity higher than 70 materialize.

Membrane Systems Engineering for Post-combustion Carbon Capture

KAUST Repository

Alshehri, Ali

2013-08-05

This study proposes a strategy for optimal design of hollow fiber membrane networks for post combustion carbon capture from power plant multicomponent flue gas. A mathematical model describing multicomponent gas permeation through a separation membrane was customized into the flowsheet modeling package ASPEN PLUS. An N-stage membrane network superstructure was defined considering all possible flowsheeting configurations. An optimization formulation was then developed and solved using an objective function that minimizes the costs associated with operating and capital expenses. For a case study of flue gas feed flow rate of 298 m3/s with 13% CO2 and under defined economic parameters, the optimization resulted in the synthesis of a membrane network structure consisting of two stages in series. This optimal design was found while also considering feed and permeate pressures as well as recycle ratios between stages. The cost of carbon capture for this optimal membrane network is estimated to be $28 per tonne of CO2 captured, considering a membrane permeance of 1000 GPU and membrane selectivity of 50. Following this approach, a reduction in capture cost to less than $20 per tonne CO2 captured is possible if membranes with permeance of 2000 GPU and selectivity higher than 70 materialize.

Subsurface capture of carbon dioxide

Science.gov (United States)

Blount, Gerald; Siddal, Alvin A.; Falta, Ronald W.

2014-07-22

A process and apparatus of separating CO.sub.2 gas from industrial off-gas source in which the CO.sub.2 containing off-gas is introduced deep within an injection well. The CO.sub.2 gases are dissolved in the, liquid within the injection well while non-CO.sub.2 gases, typically being insoluble in water or brine, are returned to the surface. Once the CO.sub.2 saturated liquid is present within the injection well, the injection well may be used for long-term geologic storage of CO.sub.2 or the CO.sub.2 saturated liquid can be returned to the surface for capturing a purified CO.sub.2 gas.

Techno-economic Comparison of Geological Disposal of Carbon Dioxide and Radioactive Waste

International Nuclear Information System (INIS)

2014-12-01

The reduction of greenhouse gas emissions is an important prerequisite for sustainable development. The energy sector is a major contributor to such emissions, which are mostly from fossil fuel fired power plants acting as point sources of carbon dioxide (CO 2 ) discharges. For the last twenty years, the new technology of carbon capture and storage, which mitigates CO 2 emissions, has been considered in many IAEA Member States. This technology involves the removal of CO 2 from the combustion process and its disposal in geological formations, such as depleted oil or gas fields, saline aquifers or unmineable coal seams. A large scale energy supply option with low CO 2 emissions is nuclear power. The high level radioactive waste produced during nuclear power plant operation and decommissioning as well as in nuclear fuel reprocessing is also planned to be disposed of in deep geological formations. To further research and development in these areas and to compare and learn from the planning, development and implementation of these two underground waste disposal concepts, the IAEA launched the coordinated research project (CRP) Techno-economic Comparison of Ultimate Disposal Facilities for Carbon Dioxide and Radioactive Waste. The project started in 2008 and was completed in 2012. The project established an international network of nine institutions from nine IAEA Member States, representing both developing and developed countries. The CRP results compared the geological disposal facilities in the following areas: geology, environmental impacts, risk and safety assessment, monitoring, cost estimation, public perception, policy, regulation and institutions. This publication documents the outcome of the CRP and is structured into thematic chapters, covering areas analysed. Each chapter was prepared under the guidance of a lead author and involved co-authors from different Member States with diverse expertise in related areas. Participants drew on the results of earlier

Pilot-Scale Silicone Process for Low-Cost Carbon Dioxide Capture

Energy Technology Data Exchange (ETDEWEB)

Singh, Surinder; Spiry, Irina; Wood, Benjamin; Hancu, Dan; Chen, Wei

2014-07-01

This report presents system and economicanalysis for a carbon-capture unit which uses an aminosilicone-based solvent for CO₂ capture in a pulverized coal (PC) boiler. The aminosilicone solvent is a 60/40 wt/wt mixture of 3-aminopropyl end-capped polydimethylsiloxane (GAP-1m) with tri-ethylene glycol (TEG) as a co-solvent. Forcomparison purposes, the report also shows results for a carbon-capture unit based on a conventional approach using mono-ethanol amine (MEA). The first year removal cost of CO₂ for the aminosilicone-based carbon-capture process is $46.04/ton of CO₂ as compared to $60.25/ton of CO₂ when MEA is used. The aminosilicone- based process has <77% of the CAPEX of a system using MEA solvent. The lower CAPEX is due to several factors, including the higher working capacity of the aminosilicone solvent compared the MEA, which reduces the solvent flow rate required, reducing equipment sizes. If it is determined that carbon steel can be used in the rich-lean heat exchanger in the carbon capture unit, the first year removal cost of CO₂ decreases to $44.12/ton. The aminosilicone-based solvent has a higherthermal stability than MEA, allowing desorption to be conducted at higher temperatures and pressures, decreasing the number of compressor stages needed. The aminosilicone-based solvent also has a lowervapor pressure, allowing the desorption to be conducted in a continuous-stirred tank reactor versus a more expensive packed column. The aminosilicone-based solvent has a lowerheat capacity, which decreases the heat load on the desorber. In summary, the amino-silicone solvent has significant advantages overconventional systems using MEA.

Basin-Scale Leakage Risks from Geologic Carbon Sequestration: Impact on Carbon Capture and Storage Energy Market Competitiveness

Energy Technology Data Exchange (ETDEWEB)

Peters, Catherine; Fitts, Jeffrey; Wilson, Elizabeth; Pollak, Melisa; Bielicki, Jeffrey; Bhatt, Vatsal

2013-03-13

This three-year project, performed by Princeton University in partnership with the University of Minnesota and Brookhaven National Laboratory, examined geologic carbon sequestration in regard to CO{sub 2} leakage and potential subsurface liabilities. The research resulted in basin-scale analyses of CO{sub 2} and brine leakage in light of uncertainties in the characteristics of leakage processes, and generated frameworks to monetize the risks of leakage interference with competing subsurface resources. The geographic focus was the Michigan sedimentary basin, for which a 3D topographical model was constructed to represent the hydrostratigraphy. Specifically for Ottawa County, a statistical analysis of the hydraulic properties of underlying sedimentary formations was conducted. For plausible scenarios of injection into the Mt. Simon sandstone, leakage rates were estimated and fluxes into shallow drinking-water aquifers were found to be less than natural analogs of CO{sub 2} fluxes. We developed the Leakage Impact Valuation (LIV) model in which we identified stakeholders and estimated costs associated with leakage events. It was found that costs could be incurred even in the absence of legal action or other subsurface interference because there are substantial costs of finding and fixing the leak and from injection interruption. We developed a model framework called RISCS, which can be used to predict monetized risk of interference with subsurface resources by combining basin-scale leakage predictions with the LIV method. The project has also developed a cost calculator called the Economic and Policy Drivers Module (EPDM), which comprehensively calculates the costs of carbon sequestration and leakage, and can be used to examine major drivers for subsurface leakage liabilities in relation to specific injection scenarios and leakage events. Finally, we examined the competiveness of CCS in the energy market. This analysis, though qualitative, shows that financial

Near-surface monitoring strategies for geologic carbon dioxide storage verification

Energy Technology Data Exchange (ETDEWEB)

Oldenburg, Curtis M.; Lewicki, Jennifer L.; Hepple, Robert P.

2003-10-31

Geologic carbon sequestration is the capture of anthropogenic carbon dioxide (CO{sub 2}) and its storage in deep geologic formations. Geologic CO{sub 2} storage verification will be needed to ensure that CO{sub 2} is not leaking from the intended storage formation and seeping out of the ground. Because the ultimate failure of geologic CO{sub 2} storage occurs when CO{sub 2} seeps out of the ground into the atmospheric surface layer, and because elevated concentrations of CO{sub 2} near the ground surface can cause health, safety, and environmental risks, monitoring will need to be carried out in the near-surface environment. The detection of a CO{sub 2} leakage or seepage signal (LOSS) in the near-surface environment is challenging because there are large natural variations in CO{sub 2} concentrations and fluxes arising from soil, plant, and subsurface processes. The term leakage refers to CO{sub 2} migration away from the intended storage site, while seepage is defined as CO{sub 2} passing from one medium to another, for example across the ground surface. The flow and transport of CO{sub 2} at high concentrations in the near-surface environment will be controlled by its high density, low viscosity, and high solubility in water relative to air. Numerical simulations of leakage and seepage show that CO{sub 2} concentrations can reach very high levels in the shallow subsurface even for relatively modest CO{sub 2} leakage fluxes. However, once CO{sub 2} seeps out of the ground into the atmospheric surface layer, surface winds are effective at dispersing CO{sub 2} seepage. In natural ecological systems with no CO{sub 2} LOSS, near-surface CO{sub 2} fluxes and concentrations are controlled by CO{sub 2} uptake by photosynthesis, and production by root respiration, organic carbon biodegradation in soil, deep outgassing of CO{sub 2}, and by exchange of CO{sub 2} with the atmosphere. Existing technologies available for monitoring CO{sub 2} in the near-surface environment

False Hope. Why carbon capture and storage won't save the climate

International Nuclear Information System (INIS)

Rochon, Emily; Kuper, Jo; Bjureby, Erika; Johnston, Paul; Oakley, Robin; Santillo, David; Schulz, Nina; Von Goerne, Gabriela

2008-05-01

Carbon capture and storage (CCS) aims to reduce the climate impact of burning fossil fuels by capturing carbon dioxide (CO 2 ) from power station smokestacks and disposing of it underground. However, the technology is largely unproven and will not be ready in time to save the climate

Post-combustion carbon capture - solid sorbents and membranes

Energy Technology Data Exchange (ETDEWEB)

Davidson, R.M.

2009-01-15

This report follows on from that on solvent scrubbing for post-combustion carbon capture from coal-fired power plants by considering the use of solid sorbents and membranes instead of solvents. First, mesoporous and microporous adsorbents are discussed: carbon-based adsorbents, zeolites, hydrotalcites and porous crystals. Attempts have been made to improve the performance of the porous adsorbent by functionalising them with nitrogen groups and specifically, amine groups to react with CO{sub 2} and thus enhance the physical adsorption properties. Dry, regenerable solid sorbents have attracted a good deal of research. Most of the work has been on the carbonation/calcination cycle of natural limestone but there have also been studies of other calcium-based sorbents and alkali metal-based sorbents. Membranes have also been studied as potential post-combustion capture devices. Finally, techno-economic studies predicting the economic performance of solid sorbents and membranes are discussed. 340 refs., 21 figs., 8 tabs.

Low-Carbon Economic Dispatching for Power Grid Integrated with Carbon Capture Power Plants and Wind Power System

Directory of Open Access Journals (Sweden)

Sheng Siqing

2015-01-01

Full Text Available Carbon emission characteristics of all kinds of power units are analyzed against the background of the low carbon economy. This paper introduces carbon trading in the dispatching model, gives full consideration to the benefit or cost of carbon emission and introduces carbon emission in the dispatching model as a decision variable so as to achieve the unity of the economy and the environmental protection of the dispatching model. A low carbon economic dispatching model is established based on multiple objectives, such as the lowest thermal power generation cost, the lowest carbon trading cost and the lowest carbon capture power plant operation cost. Load equalization, output constraint of power unit, ramping constraint, spinning reserve constraint and carbon capture efficiency constraint should be taken into account in terms of constraint conditions. The model is solved by the particle swarm optimization based on dynamic exchange and density distance. The fact that the introduction of carbon trading can effectively reduce the level of carbon emission and increase the acceptance level of wind power is highlighted through the comparison of the results of three models’ computational examples. With the carbon trading mechanism, carbon capture power plants with new technologies are able to give full play to the advantage of reducing carbon emission and wind curtailment so as to promote the development of the energy conservation and emission reduction technology and reduce the total cost of the dispatching system.

Carbon capture from coal fired power plant using pressurized fluid bed technology

Energy Technology Data Exchange (ETDEWEB)

Williams, Dennis; Christensen, Tor

2010-09-15

This presentation will discuss the use of a pressurized fluid bed boiler system and specialized carbon capture system to burn coal and generagte clean electricity. The paper will present the existing boiler and carbon capture technology and present economics, thermal performance and emissions reduction for a 100Mw module.

Carbon capture and storage-Investment strategies for the future?

International Nuclear Information System (INIS)

Rammerstorfer, Margarethe; Eisl, Roland

2011-01-01

The following article deals with real options modeling for investing into carbon capture and storage technologies. Herein, we derive two separate models. The first model incorporates a constant convenience yield and dividend for the investment project. In the second model, the convenience yield is allowed to follow a mean reverting process which seems to be more realistic, but also increases the model's complexity. Both frameworks are to be solved numerically. Therefore, we calibrate our model with respect to empirical data and provide insights into the models' sensitivity toward the chosen parameter values. We found that given the recently observable prices for carbon dioxide, an investment into C O2-storage facilities is not profitable. - Highlights: → Real options modeling for investing into carbon capture and storage technologies. → Given the recently observable prices for carbon dioxide, an investment into CO 2 -storage facilities is not profitable. → Investment decision is mainly affected by risk free rate and volatility.

Constraining climate sensitivity and continental versus seafloor weathering using an inverse geological carbon cycle model.

Science.gov (United States)

Krissansen-Totton, Joshua; Catling, David C

2017-05-22

The relative influences of tectonics, continental weathering and seafloor weathering in controlling the geological carbon cycle are unknown. Here we develop a new carbon cycle model that explicitly captures the kinetics of seafloor weathering to investigate carbon fluxes and the evolution of atmospheric CO 2 and ocean pH since 100 Myr ago. We compare model outputs to proxy data, and rigorously constrain model parameters using Bayesian inverse methods. Assuming our forward model is an accurate representation of the carbon cycle, to fit proxies the temperature dependence of continental weathering must be weaker than commonly assumed. We find that 15-31 °C (1σ) surface warming is required to double the continental weathering flux, versus 3-10 °C in previous work. In addition, continental weatherability has increased 1.7-3.3 times since 100 Myr ago, demanding explanation by uplift and sea-level changes. The average Earth system climate sensitivity is  K (1σ) per CO 2 doubling, which is notably higher than fast-feedback estimates. These conclusions are robust to assumptions about outgassing, modern fluxes and seafloor weathering kinetics.

Erosion of organic carbon in the Arctic as a geological carbon dioxide sink.

Science.gov (United States)

Hilton, Robert G; Galy, Valier; Gaillardet, Jérôme; Dellinger, Mathieu; Bryant, Charlotte; O'Regan, Matt; Gröcke, Darren R; Coxall, Helen; Bouchez, Julien; Calmels, Damien

2015-08-06

Soils of the northern high latitudes store carbon over millennial timescales (thousands of years) and contain approximately double the carbon stock of the atmosphere. Warming and associated permafrost thaw can expose soil organic carbon and result in mineralization and carbon dioxide (CO2) release. However, some of this soil organic carbon may be eroded and transferred to rivers. If it escapes degradation during river transport and is buried in marine sediments, then it can contribute to a longer-term (more than ten thousand years), geological CO2 sink. Despite this recognition, the erosional flux and fate of particulate organic carbon (POC) in large rivers at high latitudes remains poorly constrained. Here, we quantify the source of POC in the Mackenzie River, the main sediment supplier to the Arctic Ocean, and assess its flux and fate. We combine measurements of radiocarbon, stable carbon isotopes and element ratios to correct for rock-derived POC. Our samples reveal that the eroded biospheric POC has resided in the basin for millennia, with a mean radiocarbon age of 5,800 ± 800 years, much older than the POC in large tropical rivers. From the measured biospheric POC content and variability in annual sediment yield, we calculate a biospheric POC flux of 2.2(+1.3)(-0.9) teragrams of carbon per year from the Mackenzie River, which is three times the CO2 drawdown by silicate weathering in this basin. Offshore, we find evidence for efficient terrestrial organic carbon burial over the Holocene period, suggesting that erosion of organic carbon-rich, high-latitude soils may result in an important geological CO2 sink.

Capturing spatial heterogeneity of soil organic carbon under changing climate

Science.gov (United States)

Mishra, U.; Fan, Z.; Jastrow, J. D.; Matamala, R.; Vitharana, U.

2015-12-01

The spatial heterogeneity of the land surface affects water, energy, and greenhouse gas exchanges with the atmosphere. Designing observation networks that capture land surface spatial heterogeneity is a critical scientific challenge. Here, we present a geospatial approach to capture the existing spatial heterogeneity of soil organic carbon (SOC) stocks across Alaska, USA. We used the standard deviation of 556 georeferenced SOC profiles previously compiled in Mishra and Riley (2015, Biogeosciences, 12:3993-4004) to calculate the number of observations that would be needed to reliably estimate Alaskan SOC stocks. This analysis indicated that 906 randomly distributed observation sites would be needed to quantify the mean value of SOC stocks across Alaska at a confidence interval of ± 5 kg m-2. We then used soil-forming factors (climate, topography, land cover types, surficial geology) to identify the locations of appropriately distributed observation sites by using the conditioned Latin hypercube sampling approach. Spatial correlation and variogram analyses demonstrated that the spatial structures of soil-forming factors were adequately represented by these 906 sites. Using the spatial correlation length of existing SOC observations, we identified 484 new observation sites would be needed to provide the best estimate of the present status of SOC stocks in Alaska. We then used average decadal projections (2020-2099) of precipitation, temperature, and length of growing season for three representative concentration pathway (RCP 4.5, 6.0, and 8.5) scenarios of the Intergovernmental Panel on Climate Change to investigate whether the location of identified observation sites will shift/change under future climate. Our results showed 12-41 additional observation sites (depending on emission scenarios) will be required to capture the impact of projected climatic conditions by 2100 on the spatial heterogeneity of Alaskan SOC stocks. Our results represent an ideal distribution

An optimization model for carbon capture & storage/utilization vs. carbon trading: A case study of fossil-fired power plants in Turkey.

Science.gov (United States)

Ağralı, Semra; Üçtuğ, Fehmi Görkem; Türkmen, Burçin Atılgan

2018-06-01

We consider fossil-fired power plants that operate in an environment where a cap and trade system is in operation. These plants need to choose between carbon capture and storage (CCS), carbon capture and utilization (CCU), or carbon trading in order to obey emissions limits enforced by the government. We develop a mixed-integer programming model that decides on the capacities of carbon capture units, if it is optimal to install them, the transportation network that needs to be built for transporting the carbon captured, and the locations of storage sites, if they are decided to be built. Main restrictions on the system are the minimum and maximum capacities of the different parts of the pipeline network, the amount of carbon that can be sold to companies for utilization, and the capacities on the storage sites. Under these restrictions, the model aims to minimize the net present value of the sum of the costs associated with installation and operation of the carbon capture unit and the transportation of carbon, the storage cost in case of CCS, the cost (or revenue) that results from the emissions trading system, and finally the negative revenue of selling the carbon to other entities for utilization. We implement the model on General Algebraic Modeling System (GAMS) by using data associated with two coal-fired power plants located in different regions of Turkey. We choose enhanced oil recovery (EOR) as the process in which carbon would be utilized. The results show that CCU is preferable to CCS as long as there is sufficient demand in the EOR market. The distance between the location of emission and location of utilization/storage, and the capacity limits on the pipes are an important factor in deciding between carbon capture and carbon trading. At carbon prices over $15/ton, carbon capture becomes preferable to carbon trading. These results show that as far as Turkey is concerned, CCU should be prioritized as a means of reducing nation-wide carbon emissions in an

CO2 CAPTURE PROJECT - AN INTEGRATED, COLLABORATIVE TECHNOLOGY DEVELOPMENT PROJECT FOR NEXT GENERATION CO2 SEPARATION, CAPTURE AND GEOLOGIC SEQUESTRATION

Energy Technology Data Exchange (ETDEWEB)

Dr. Helen Kerr

2003-08-01

The CO{sub 2} Capture Project (CCP) is a joint industry project, funded by eight energy companies (BP, ChevronTexaco, EnCana, Eni, Norsk Hydro, Shell, Statoil, and Suncor) and three government agencies (1) European Union (DG Res & DG Tren), (2) Norway (Klimatek) and (3) the U.S.A. (Department of Energy). The project objective is to develop new technologies, which could reduce the cost of CO{sub 2} capture and geologic storage by 50% for retrofit to existing plants and 75% for new-build plants. Technologies are to be developed to ''proof of concept'' stage by the end of 2003. The project budget is approximately $24 million over 3 years and the work program is divided into eight major activity areas: (1) Baseline Design and Cost Estimation--defined the uncontrolled emissions from each facility and estimate the cost of abatement in $/tonne CO{sub 2}. (2) Capture Technology, Post Combustion: technologies, which can remove CO{sub 2} from exhaust gases after combustion. (3) Capture Technology, Oxyfuel: where oxygen is separated from the air and then burned with hydrocarbons to produce an exhaust with high CO{sub 2} for storage. (4) Capture Technology, Pre -Combustion: in which, natural gas and petroleum coke are converted to hydrogen and CO{sub 2} in a reformer/gasifier. (5) Common Economic Model/Technology Screening: analysis and evaluation of each technology applied to the scenarios to provide meaningful and consistent comparison. (6) New Technology Cost Estimation: on a consistent basis with the baseline above, to demonstrate cost reductions. (7) Geologic Storage, Monitoring and Verification (SMV): providing assurance that CO{sub 2} can be safely stored in geologic formations over the long term. (8) Non-Technical: project management, communication of results and a review of current policies and incentives governing CO{sub 2} capture and storage. Technology development work dominated the past six months of the project. Numerous studies are making

Pilot-Scale Evaluation of an Advanced Carbon Sorbent-Based Process for Post-Combustion Carbon Capture

Energy Technology Data Exchange (ETDEWEB)

Hornbostel, Marc [SRI International, Menlo Park, CA (United States)

2016-09-01

The overall objective of this project is to achieve the DOE’s goal to develop advanced CO₂ capture and separation technologies that can realize at least 90% CO₂ removal from flue gas steams produced at a pulverized coal (PC) power plant at a cost of less than $40/tonne of CO₂ captured. The principal objective is to test a CO₂ capture process that will reduce the parasitic plant load by using a CO₂ capture sorbent that will require a reduced amount of steam. The process is based on advanced carbon sorbents having a low heat of adsorption, high CO₂ adsorption capacity, and excellent selectivity. While the intent of this project was to produce design and performance data by testing the sorbent using a slipstream of coal-derived flue gas at the National Carbon Capture Center (NCCC) under realistic conditions and continuous long-term operation, the project was terminated following completion of the detailing pilot plant design/engineering work on June 30, 2016.

Assessment of Brine Management for Geologic Carbon Sequestration

Energy Technology Data Exchange (ETDEWEB)

Breunig, Hanna M. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division; Birkholzer, Jens T. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division; Borgia, Andrea [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division; Price, Phillip N. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division; Oldenburg, Curtis M. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division; McKone, Thomas E. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Environmental Energy Technologies Division

2013-06-13

Geologic carbon sequestration (GCS) is the injection of carbon dioxide (CO₂), typically captured from stationary emission sources, into deep geologic formations to prevent its entry into the atmosphere. Active pilot facilities run by regional United States (US) carbon sequestration partnerships inject on the order of one million metric tonnes (mt) CO₂ annually while the US electric power sector emits over 2000 million mt-CO₂ annually. GCS is likely to play an increasing role in US carbon mitigation initiatives, but scaling up GCS poses several challenges. Injecting CO₂ into sedimentary basins raises fluid pressure in the pore space, which is typically already occupied by naturally occurring, or native, brine. The resulting elevated pore pressures increase the likelihood of induced seismicity, of brine or CO₂ escaping into potable groundwater resources, and of CO₂ escaping into the atmosphere. Brine extraction is one method for pressure management, in which brine in the injection formation is brought to the surface through extraction wells. Removal of the brine makes room for the CO₂ and decreases pressurization. Although the technology required for brine extraction is mature, this form of pressure management will only be applicable if there are cost-­effective and sustainable methods of disposing of the extracted brine. Brine extraction, treatment, and disposal may increase the already substantial capital, energy, and water demands of Carbon dioxide Capture and Sequestration (CCS). But, regionally specific brine management strategies may be able to treat the extracted water as a source of revenue, energy, and water to subsidize CCS costs, while minimizing environmental impacts. By this approach, value from the extracted water would be recovered before disposing of any resulting byproducts. Until a price is placed on carbon, we expect that utilities and other CO₂ sources will be

Metamodeling-based approach for risk assessment and cost estimation: Application to geological carbon sequestration planning

Science.gov (United States)

Sun, Alexander Y.; Jeong, Hoonyoung; González-Nicolás, Ana; Templeton, Thomas C.

2018-04-01

Carbon capture and storage (CCS) is being evaluated globally as a geoengineering measure for significantly reducing greenhouse emission. However, long-term liability associated with potential leakage from these geologic repositories is perceived as a main barrier of entry to site operators. Risk quantification and impact assessment help CCS operators to screen candidate sites for suitability of CO2 storage. Leakage risks are highly site dependent, and a quantitative understanding and categorization of these risks can only be made possible through broad participation and deliberation of stakeholders, with the use of site-specific, process-based models as the decision basis. Online decision making, however, requires that scenarios be run in real time. In this work, a Python based, Leakage Assessment and Cost Estimation (PyLACE) web application was developed for quantifying financial risks associated with potential leakage from geologic carbon sequestration sites. PyLACE aims to assist a collaborative, analytic-deliberative decision making processes by automating metamodel creation, knowledge sharing, and online collaboration. In PyLACE, metamodeling, which is a process of developing faster-to-run surrogates of process-level models, is enabled using a special stochastic response surface method and the Gaussian process regression. Both methods allow consideration of model parameter uncertainties and the use of that information to generate confidence intervals on model outputs. Training of the metamodels is delegated to a high performance computing cluster and is orchestrated by a set of asynchronous job scheduling tools for job submission and result retrieval. As a case study, workflow and main features of PyLACE are demonstrated using a multilayer, carbon storage model.

Post combustion carbon capture - solid sorbents and membranes

Energy Technology Data Exchange (ETDEWEB)

Davidson, R.M. [IEA Clean Coal Centre, London (United Kingdom)

2009-04-15

This report follows on from that on solvent scrubbing for post-combustion carbon capture from coal-fired power plants by considering the use of solid sorbents and membranes instead of solvents. First, mesoporous and microporous adsorbents are discussed: carbon-based adsorbents, zeolites, hydrotalcites and porous crystals. Attempts have been made to improve the performance of the porous adsorbent by functionalising them with nitrogen groups and specifically, amine groups to react with CO{sub 2} and thus enhance the physical adsorption properties. Dry, regenerable solid sorbents have attracted a good deal of research. Most of the work has been on the carbonation/calcination cycle of natural limestone but there have also been studies of other calcium-based sorbents and alkali metal-based sorbents. Membranes have also been studied as potential post-combustion capture devices. Finally, techno-economic studies predicting the economic performance of solid sorbents and membranes are discussed. The report is available from IEA Clean Coal Centre as report no. CCC/144. See Coal Abstracts entry April 2009 00406. 340 refs., 21 figs., 8 tabs.

On leakage and seepage from geological carbon sequestration sites

Energy Technology Data Exchange (ETDEWEB)

Oldenburg, C.M.; Unger, A.J.A.; Hepple, R.P.; Jordan, P.D.

2002-07-18

Geologic carbon sequestration is one strategy for reducing the rate of increase of global atmospheric carbon dioxide (CO{sub 2} ) concentrations (IEA, 1997; Reichle, 2000). As used here, the term geologic carbon sequestration refers to the direct injection of supercritical CO{sub 2} deep into subsurface target formations. These target formations will typically be either depleted oil and gas reservoirs, or brine-filled permeable formations referred to here as brine formations. Injected CO{sub 2} will tend to be trapped by one or more of the following mechanisms: (1) permeability trapping, for example when buoyant supercritical CO{sub 2} rises until trapped by a confining caprock; (2) solubility trapping, for example when CO{sub 2} dissolves into the aqueous phase in water-saturated formations, or (3) mineralogic trapping, such as occurs when CO{sub 2} reacts to produce stable carbonate minerals. When CO{sub 2} is trapped in the subsurface by any of these mechanisms, it is effectively sequestered away from the atmosphere where it would otherwise act as a greenhouse gas. The purpose of this report is to summarize our work aimed at quantifying potential CO{sub 2} seepage due to leakage from geologic carbon sequestration sites. The approach we take is to present first the relevant properties of CO{sub 2} over the range of conditions from the deep subsurface to the vadose zone (Section 2), and then discuss conceptual models for how leakage might occur (Section 3). The discussion includes consideration of gas reservoir and natural gas storage analogs, along with some simple estimates of seepage based on assumed leakage rates. The conceptual model discussion provides the background for the modeling approach wherein we focus on simulating transport in the vadose zone, the last potential barrier to CO{sub 2} seepage (Section 4). Because of the potentially wide range of possible properties of actual future geologic sequestration sites, we carry out sensitivity analyses by

Integrating geothermal into coal-fired power plant with carbon capture: A comparative study with solar energy

International Nuclear Information System (INIS)

Wang, Fu; Deng, Shuai; Zhao, Jun; Zhao, Jiapei; Yang, Guohua; Yan, Jinyue

2017-01-01

Highlights: • Post-combustion carbon capture integrating geothermal energy was proposed. • A 300 MWe subcritical coal-fired plant was selected as the baseline. • The geothermal assisted carbon capture system was compared with solar assisted carbon capture plant. • Two different locations were chosen for the technical and economical comparison. • Using medium temperature geothermal thermal energy to replace steam extraction performs better performance. - Abstract: A new system integrating geothermal energy into post-combustion carbon capture is proposed in this paper. Geothermal energy at medium temperatures is used to provide the required thermal heat for solvent regeneration. The performance of this system is compared with solar assisted carbon capture plant via technical and economic evaluation. A 300 MWe coal-fired power plant is selected as the reference case, and two different locations based on the local climatic conditions and geothermal resources are chosen for the comparison. The results show that the geothermal assisted post-combustion carbon capture plant has better performances than the solar assisted one in term of the net power output and annual electricity generation. The net plant average efficiency based on lower heating value can be increased by 2.75% with a thermal load fraction of about 41%. Results of economic assessment show that the proposed geothermal assisted post-combustion carbon capture system has lower levelized costs of electricity and cost of carbon dioxide avoidance compared to the solar assisted post-combustion carbon capture plant. In order to achieve comparative advantages over the reference post-combustion carbon capture plant in both locations, the price of solar collector has to be lower than 70 USD/m 2 , and the drilling depth of the geothermal well shall be less than 2.1 km.

Technology Roadmaps: Carbon Capture and Storage in Industrial Applications

Energy Technology Data Exchange (ETDEWEB)

NONE

2011-07-01

A new technology roadmap on Carbon Capture and Storage in Industrial Applications, released today in Beijing, shows that carbon capture and storage (CCS) has the potential to reduce CO2 emissions from industrial applications by 4 gigatonnes in 2050. Such an amount is equal to roughly one-tenth of the total emission cuts needed from the energy sector by the middle of the century. This requires a rapid deployment of CCS technologies in various industrial sectors, and across both OECD and non-OECD countries. The roadmap, a joint report from the International Energy Agency (IEA) and the United Nations Industrial Development Organization (UNIDO), says that over 1800 industrial-scale projects are required over the next 40 years.

Carbon Capture and Sequestration (via Enhanced Oil Recovery) from a Hydrogen Production Facility in an Oil Refinery

Energy Technology Data Exchange (ETDEWEB)

Stewart Mehlman

2010-06-16

The project proposed a commercial demonstration of advanced technologies that would capture and sequester CO2 emissions from an existing hydrogen production facility in an oil refinery into underground formations in combination with Enhanced Oil Recovery (EOR). The project is led by Praxair, Inc., with other project participants: BP Products North America Inc., Denbury Onshore, LLC (Denbury), and Gulf Coast Carbon Center (GCCC) at the Bureau of Economic Geology of The University of Texas at Austin. The project is located at the BP Refinery at Texas City, Texas. Praxair owns and operates a large hydrogen production facility within the refinery. As part of the project, Praxair would construct a CO2 capture and compression facility. The project aimed at demonstrating a novel vacuum pressure swing adsorption (VPSA) based technology to remove CO2 from the Steam Methane Reformers (SMR) process gas. The captured CO2 would be purified using refrigerated partial condensation separation (i.e., cold box). Denbury would purchase the CO2 from the project and inject the CO2 as part of its independent commercial EOR projects. The Gulf Coast Carbon Center at the Bureau of Economic Geology, a unit of University of Texas at Austin, would manage the research monitoring, verification and accounting (MVA) project for the sequestered CO2, in conjunction with Denbury. The sequestration and associated MVA activities would be carried out in the Hastings field at Brazoria County, TX. The project would exceed DOE’s target of capturing one million tons of CO2 per year (MTPY) by 2015. Phase 1 of the project (Project Definition) is being completed. The key objective of Phase 1 is to define the project in sufficient detail to enable an economic decision with regard to proceeding with Phase 2. This topical report summarizes the administrative, programmatic and technical accomplishments completed in Phase 1 of the project. It describes the work relative to project technical and design activities

CO2 emission standards and investment in carbon capture

International Nuclear Information System (INIS)

Eide, Jan; Sisternes, Fernando J. de; Herzog, Howard J.; Webster, Mort D.

2014-01-01

Policy makers in a number of countries have proposed or are considering proposing CO 2 emission standards for new fossil fuel-fired power plants. The proposed standards require coal-fired power plants to have approximately the same carbon emissions as an uncontrolled natural gas-fired power plant, effectively mandating the adoption of carbon capture and sequestration (CCS) technologies for new coal plants. However, given the uncertainty in the capital and operating costs of a commercial scale coal plant with CCS, the impact of such a standard is not apparent a priori. We apply a stochastic generation expansion model to determine the impact of CO 2 emission standards on generation investment decisions, and in particular for coal plants with CCS. Moreover, we demonstrate how the incentive to invest in coal-CCS from emission standards depends on the natural gas price, the CO 2 price, and the enhanced oil recovery price, as well as on the level of the emission standard. This analysis is the first to consider the entire power system and at the same time allow the capture percentage for CCS plants to be chosen from a continuous range to meet the given standard at minimum cost. Previous system level studies have assumed that CCS plants capture 90% of the carbon, while studies of individual units have demonstrated the costs of carbon capture over a continuous range. We show that 1) currently proposed levels of emission standards are more likely to shift fossil fuel generation from coal to natural gas rather than to incentivize investment in CCS; 2) tighter standards that require some carbon reductions from natural gas-fired power plants are more likely than proposed standards to incentivize investments in CCS, especially on natural gas plants, but also on coal plants at high gas prices; and 3) imposing a less strict emission standard (emission rates higher than natural gas but lower than coal; e.g., 1500 lbs/MWh) is more likely than current proposals to incentivize

Carbon Capture and Storage in the CDM

Energy Technology Data Exchange (ETDEWEB)

NONE

2007-07-01

This publication assesses the policy questions as highlighted in the relevant COP/MOP 2 decision, particularly leaks (or seepage) and permanence for geological storage, project boundaries and liability issues, and leakage, as well as a few others raised by some Parties. Since any emissions or leaks during the separation, capture and transport phases would occur during the crediting period of the project (and would therefore be accounted for as project emissions), the paper focuses its analyses for leaks and liability on storage, as it is in this part of the CCS process that long-term leaks could occur.

Capture and geological sequestration of CO2: fighting against global warming

International Nuclear Information System (INIS)

Czernichowski-Lauriol, I.

2006-01-01

In order to take up the global warming challenge, a set of emergency measures is to be implemented: energy saving, clean transportation systems, development of renewable energy sources.. CO 2 sequestration of massive industrial emission sources inside deep geologic formations is another promising solution, which can contribute to the division by two of the world CO 2 emissions between today and 2050. The CO 2 capture and sequestration industry is developing. Research projects and pilot facilities are on the increase over the world. Their aim is to warrant the efficiency and security of this technology over the centuries to come. (J.S.)

How green can black be? Assessing the potential for equipping USA's existing coal fleet with carbon capture and storage

Science.gov (United States)

Patrizio, Piera; Leduc, Sylvain; Mesfun, Sennai; Yowargana, Ping; Kraxner, Florian

2017-04-01

The mitigation of adverse environmental impacts due to climate change requires the reduction of carbon dioxide emissions - also from the U.S. energy sector, a dominant source of greenhouse-gas emissions. This is especially true for the existing fleet of coal-fired power plants, accounting for roughly two-thirds of the U.S. energy sectors' total CO2 emissions. With this aim, different carbon mitigation options have been proposed in literature, such as increasing the energy efficiency, co-firing of biomass and/or the adoption of carbon capturing technologies (BECCS). However, the extent to which these solutions can be adopted depends on a suite of site specific factors and therefore needs to be evaluated on a site-specific basis. We propose a spatially explicit approach to identify candidate coal plants for which carbon capture technologies are economically feasible, according to different economic and policy frameworks. The methodology implies the adoption of IIASA's techno economic model BeWhere, which optimizes the cost of the entire BECCS supply chain, from the biomass resources to the storage of the CO2 in the nearest geological sink. The results shows that biomass co-firing appears to be the most appealing economic solution for a larger part of the existing U.S. coal fleet, while the adoption of CCS technologies is highly dependent on the level of CO2 prices as well as on local factors such as the type of coal firing technology and proximity of storage sites.

Carbon capture and storage (CCS): the way forward

OpenAIRE

Bui, Mai; Adjiman, Claire S.; Bardow, André; Anthony, Edward J.; Boston, Andy; Brown, Solomon; Fennell, Paul S.; Fuss, Sabine; Galindo, Amparo; Hackett, Leigh A.; Hallett, Jason P.; Herzog, Howard J.; Jackson, George; Kemper, Jasmin; Krevor, Samuel

2018-01-01

Carbon capture and storage (CCS) is broadly recognised as having the potential to play a key role in meeting climate change targets, delivering low carbon power, decarbonising industry and, more recently, its ability to facilitate the net removal of CO2 from the atmosphere. However, despite this broad consensus and technical maturity, CCS has not yet been deployed on a scale commensurate with the ambitions articulated a decade ago. Thus, in this paper we review the current stat...

Carbon Capture and Storage: Legal and Regulatory Review

Energy Technology Data Exchange (ETDEWEB)

NONE

2010-07-01

The International Energy Agency (IEA) considers carbon capture and storage (CCS) a crucial part of worldwide efforts to limit global warming by reducing greenhouse-gas emissions. The IEA has estimated that the broad deployment of low-carbon energy technologies could reduce projected 2050 emissions to half 2005 levels -- and that CCS could contribute about one-fifth of those reductions. Reaching that goal, however, would require around 100 CCS projects to be implemented by 2020 and over 3000 by 2050.

CO{sub 2} capture by adsorption with nitrogen enriched carbons

Energy Technology Data Exchange (ETDEWEB)

M.G. Plaza; C. Pevida; A. Arenillas; F. Rubiera; J.J. Pis [Instituto Nacional del Carbon (CSIC), Oviedo (Spain)

2007-09-15

The success of CO{sub 2} capture with solid sorbents is dependent on the development of a low cost sorbent with high CO{sub 2} selectivity and adsorption capacity. Immobilised amines are expected to offer the benefits of liquid amines in the typical absorption process, with the added advantages that solids are easy to handle and that they do not give rise to corrosion problems. In this work, different alkylamines were evaluated as a potential source of basic sites for CO{sub 2} capture, and a commercial activated carbon was used as a preliminary support in order to study the effect of the impregnation. The amine coating increased the basicity and nitrogen content of the carbon. However, it drastically reduced the microporous volume of the activated carbon, which is chiefly responsible for CO{sub 2} physisorption, thus decreasing the capacity of raw carbon at room temperature. 33 refs., 7 figs., 3 tabs.

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

Energy Technology Data Exchange (ETDEWEB)

David A. Green; Brian S. Turk; Raghubir P. Gupta; Alejandro Lopez-Ortiz; Douglas P. Harrison; Ya Liang

2001-07-01

Sodium based sorbents including sodium carbonate may be used to capture carbon dioxide from flue gas. A relatively concentrated carbon dioxide stream may be recoverable for sequestration when the sorbent is regenerated. Electrobalance tests indicated that sodium carbonate monohydrate was formed in a mixture of helium and water vapor at temperatures below 65 C. Additional compounds may also form, but this could not be confirmed. In the presence of carbon dioxide and water vapor, both the initial reaction rate of sodium carbonate with carbon dioxide and water and the sorbent capacity decreased with increasing temperature, consistent with the results from the previous quarter. Increasing the carbon dioxide concentration at constant temperature and water vapor concentration produced a measurable increase in rate, as did increasing the water vapor concentration at constant carbon dioxide concentration and temperature. Runs conducted with a flatter TGA pan resulted in a higher initial reaction rate, presumably due to improved gas-solid contact, but after a short time, there was no significant difference in the rates measured with the different pans. Analyses of kinetic data suggest that the surface of the sodium carbonate particles may be much hotter than the bulk gas due to the highly exothermic reaction with carbon dioxide and water, and that the rate of heat removal from the particle may control the reaction rate. A material and energy balance was developed for a cyclic carbonation/calcination process which captures about 26 percent of the carbon dioxide present in flue gas available at 250 C.

Program Energy of the CNRS. Topic 10 combustion and capture of CO{sub 2}. PRI 10.1. Capture by adsorption of the CO{sub 2} in thermal power plants gas and their injection in petroleum wells. Final report period 2002-2004; Programme energie du CNRS. Theme 10 combustion et capture du CO2. PRI 10.1. Capture par adsorption du CO2 dans des gaz de centrales thermiques et leur injection en puits de petrole. Rapport final periode 2002-2004

Energy Technology Data Exchange (ETDEWEB)

Tondeur, D

2005-07-01

In the framework of the global warming resulting of the greenhouse gases emission increase, the carbon dioxide capture and storage in deep underground cavities of old petroleum and gas deposits, are studied. This report presents the researches realized by the CNRS (France) in the domain: technology and knowledge assessment concerning the carbon dioxide capture and storage, active coals for the CO{sub 2} capture, methodology of thermo-economical optimization of the combined cycle, global simulation of an IGCC (Integrated gasification combined cycle) with CO{sub 2} capture and integration in the process scheme, petroleum recovery-aided by CO{sub 2} injection, storage in geological deposits. (A.L.B.)

System-level modeling for geological storage of CO2

OpenAIRE

Zhang, Yingqi; Oldenburg, Curtis M.; Finsterle, Stefan; Bodvarsson, Gudmundur S.

2006-01-01

One way to reduce the effects of anthropogenic greenhouse gases on climate is to inject carbon dioxide (CO2) from industrial sources into deep geological formations such as brine formations or depleted oil or gas reservoirs. Research has and is being conducted to improve understanding of factors affecting particular aspects of geological CO2 storage, such as performance, capacity, and health, safety and environmental (HSE) issues, as well as to lower the cost of CO2 capture and related p...

Carbon Capture and Storage and Carbon Capture and Utilization: What Do They Offer to Indonesia?

Energy Technology Data Exchange (ETDEWEB)

Adisaputro, Didi, E-mail: didiadisaputro@gmail.com [Department of Chemical and Biological Engineering, University of Sheffield, Sheffield (United Kingdom); Department of Energy Security, Indonesian Defence University, Bogor (Indonesia); Saputra, Bastian [Department of Chemical and Biological Engineering, University of Sheffield, Sheffield (United Kingdom)

2017-03-30

Indonesia is a developing country with abundance resource of fossil fuel in the world, and this fossil fuel will remain as the main source of energy over the next few decades. However, the Indonesian Government has committed to reducing greenhouse gas emissions from fossil fuel consumption as an effort to mitigate climate change. In view of this, two possible energy scenarios are envisioned to honor this commitment: “business as usual” (BaU) and the National Energy Policy (NEP) scenario (National Energy Council, 2014). The NEP scenario reduces CO{sub 2} emissions by up to 26% through an improved energy mix, less reliance on carbon-based fuels, and the deployment of renewable energy sources from 2020 to 2050. However, these actions are considered insufficient to further reduce the CO{sub 2} emission target, leading to an initiative to implement carbon capture and storage (CCS) technology.

An integrated approach to geological disposal of UK wastes containing carbon-14

International Nuclear Information System (INIS)

Vines, Sarah; Lever, David

2013-01-01

Carbon-14 is a key radionuclide in the assessment of the safety of a geological disposal facility for radioactive waste because of the calculated assessment of the radiological consequences of gaseous carbon-14 bearing species [i]. It may be that such calculations are based on overly conservative assumptions and that better understanding could lead to considerably reduced assessment of the radiological consequences from these wastes. Alternatively, it may be possible to mitigate the impact of these wastes through alternative treatment, packaging or design options. The Radioactive Waste Management Directorate of the UK's Nuclear Decommissioning Authority (NDA RWMD) has established an integrated project team in which the partners are working together to develop a holistic approach to carbon-14 management in the disposal system [ii]. For a waste stream containing carbon-14 to be an issue: There must be a significant inventory of carbon-14 in the waste stream; and That waste stream has to generate carbon-14 bearing gas; and a bulk gas phase has to entrain the carbon-14 bearing gas: and these gases must migrate through the engineered barriers in significant quantities; and these gases must migrate through the overlying geological environment (either as a distinct gas phase or as dissolved gas); and these gases must interact with materials in the biosphere (i.e. plants) in a manner that leads to significant doses and risks to exposed groups or potentially exposed groups. The project team has developed and used this 'and' approach to structure and prioritise the technical work and break the problem down in a manageable way. We have also used it to develop our approach to considering alternative treatment, packaging and design options. For example, it may be possible to pre-treat some wastes to remove some of the inventory or to segregate other wastes so that they are removed from any bulk gas phase which might facilitate migration through the geosphere

An integrated approach to geological disposal of UK wastes containing carbon-14

Energy Technology Data Exchange (ETDEWEB)

Vines, Sarah [Nuclear Decommissioning Authority, Harwell, Oxfordshire (United Kingdom); Lever, David [AMEC, Harwell, Oxfordshire (United Kingdom)

2013-07-01

Carbon-14 is a key radionuclide in the assessment of the safety of a geological disposal facility for radioactive waste because of the calculated assessment of the radiological consequences of gaseous carbon-14 bearing species [i]. It may be that such calculations are based on overly conservative assumptions and that better understanding could lead to considerably reduced assessment of the radiological consequences from these wastes. Alternatively, it may be possible to mitigate the impact of these wastes through alternative treatment, packaging or design options. The Radioactive Waste Management Directorate of the UK's Nuclear Decommissioning Authority (NDA RWMD) has established an integrated project team in which the partners are working together to develop a holistic approach to carbon-14 management in the disposal system [ii]. For a waste stream containing carbon-14 to be an issue: There must be a significant inventory of carbon-14 in the waste stream; and That waste stream has to generate carbon-14 bearing gas; and a bulk gas phase has to entrain the carbon-14 bearing gas: and these gases must migrate through the engineered barriers in significant quantities; and these gases must migrate through the overlying geological environment (either as a distinct gas phase or as dissolved gas); and these gases must interact with materials in the biosphere (i.e. plants) in a manner that leads to significant doses and risks to exposed groups or potentially exposed groups. The project team has developed and used this 'and' approach to structure and prioritise the technical work and break the problem down in a manageable way. We have also used it to develop our approach to considering alternative treatment, packaging and design options. For example, it may be possible to pre-treat some wastes to remove some of the inventory or to segregate other wastes so that they are removed from any bulk gas phase which might facilitate migration through the geosphere

Active chemisorption sites in functionalized ionic liquids for carbon capture.

Science.gov (United States)

Cui, Guokai; Wang, Jianji; Zhang, Suojiang

2016-07-25

Development of novel technologies for the efficient and reversible capture of CO2 is highly desired. In the last decade, CO2 capture using ionic liquids has attracted intensive attention from both academia and industry, and has been recognized as a very promising technology. Recently, a new approach has been developed for highly efficient capture of CO2 by site-containing ionic liquids through chemical interaction. This perspective review focuses on the recent advances in the chemical absorption of CO2 using site-containing ionic liquids, such as amino-based ionic liquids, azolate ionic liquids, phenolate ionic liquids, dual-functionalized ionic liquids, pyridine-containing ionic liquids and so on. Other site-containing liquid absorbents such as amine-based solutions, switchable solvents, and functionalized ionic liquid-amine blends are also investigated. Strategies have been discussed for how to activate the existent reactive sites and develop novel reactive sites by physical and chemical methods to enhance CO2 absorption capacity and reduce absorption enthalpy. The carbon capture mechanisms of these site-containing liquid absorbents are also presented. Particular attention has been paid to the latest progress in CO2 capture in multiple-site interactions by amino-free anion-functionalized ionic liquids. In the last section, future directions and prospects for carbon capture by site-containing ionic liquids are outlined.

The mechanism of selective molecular capture in carbon nanotube networks.

Science.gov (United States)

Wan, Yu; Guan, Jun; Yang, Xudong; Zheng, Quanshui; Xu, Zhiping

2014-07-28

Recently, air pollution issues have drawn significant attention to the development of efficient air filters, and one of the most promising materials for this purpose is nanofibers. We explore here the mechanism of selective molecular capture of volatile organic compounds in carbon nanotube networks by performing atomistic simulations. The results are discussed with respect to the two key parameters that define the performance of nanofiltration, i.e. the capture efficiency and flow resistance, which demonstrate the advantages of carbon nanotube networks with high surface-to-volume ratio and atomistically smooth surfaces. We also reveal the important roles of interfacial adhesion and diffusion that govern selective gas transport through the network.

Program Energy of the CNRS. Topic 10 combustion and capture of CO2. PRI 10.1. Capture by adsorption of the CO2 in thermal power plants gas and their injection in petroleum wells. Final report period 2002-2004

International Nuclear Information System (INIS)

Tondeur, D.

2005-01-01

In the framework of the global warming resulting of the greenhouse gases emission increase, the carbon dioxide capture and storage in deep underground cavities of old petroleum and gas deposits, are studied. This report presents the researches realized by the CNRS (France) in the domain: technology and knowledge assessment concerning the carbon dioxide capture and storage, active coals for the CO 2 capture, methodology of thermo-economical optimization of the combined cycle, global simulation of an IGCC (Integrated gasification combined cycle) with CO 2 capture and integration in the process scheme, petroleum recovery-aided by CO 2 injection, storage in geological deposits. (A.L.B.)

Geologic CO₂ Sequestration Potential of 42 California Power Plant Sites: A Status Report to WESTCARB

Energy Technology Data Exchange (ETDEWEB)

Myers, Katherine B.L. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Wagoner, J. L. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2011-06-15

Forty-two California natural gas combined-cycle (NGCC) power plant sites were evaluated for geologic carbon dioxide (CO₂) sequestration potential. The following data were collected in order to gauge the sequestration potential of each power plant site: nearest potential CO₂ sink, proximity to oil or gas fi elds, subsurface geology, surface expression of nearby faults, and subsurface water. The data for each site were compiled into a one-page, standalone profi le to serve as a quick reference for future decision-makers. A subset of these data was compiled into a summary table for easy comparison of all 42 sites. Decision-makers will consider the geologic CO₂ sequestration potential of each power plant in concert with its CO₂ capture potential and will select the most suitable sites for a future carbon capture and storage project. Once the most promising sites are selected, Lawrence Livermore National Laboratory (LLNL) will conduct additional geologic research in order to construct a detailed 3D geologic model for those sites.

Determinants of the costs of carbon capture and sequestration for expanding electricity generation capacity

International Nuclear Information System (INIS)

Giovanni, Emily; Richards, Kenneth R.

2010-01-01

This study models the costs of electricity generation with carbon capture and sequestration (CCS), from generation at the power plant to carbon injection at the reservoir, examining the economic factors that affect technology choice and CCS costs at the individual plant level. The results suggest that natural gas and coal prices have profound impacts on the carbon price needed to induce CCS. To extend previous analyses we develop a 'cost region' graph that models technology choice as a function of carbon and fuel prices. Generally, the least-cost technology at low carbon prices is pulverized coal, while intermediate carbon prices favor natural gas technologies and high carbon prices favor coal gasification with capture. However, the specific carbon prices at which these transitions occur is largely determined by the price of natural gas. For instance, the CCS-justifying carbon price ranges from $27/t CO 2 at high natural gas prices to $54/t CO 2 at low natural gas prices. This result has important implications for potential climate change legislation. The capital costs of the generation and CO 2 capture plant are also highly important, while pipeline distance and criteria pollutant control are less significant.

Modeling geologic storage of carbon dioxide: Comparison of non-hysteretic and hysteretic characteristic curves

International Nuclear Information System (INIS)

Doughty, Christine

2007-01-01

Numerical models of geologic storage of carbon dioxide (CO 2 ) in brine-bearing formations use characteristic curves to represent the interactions of non-wetting-phase CO 2 and wetting-phase brine. When a problem includes both injection of CO 2 (a drainage process) and its subsequent post-injection evolution (a combination of drainage and wetting), hysteretic characteristic curves are required to correctly capture the behavior of the CO 2 plume. In the hysteretic formulation, capillary pressure and relative permeability depend not only on the current grid-block saturation, but also on the history of the saturation in the grid block. For a problem that involves only drainage or only wetting, a non-hysteretic formulation, in which capillary pressure and relative permeability depend only on the current value of the grid-block saturation, is adequate. For the hysteretic formulation to be robust computationally, care must be taken to ensure the differentiability of the characteristic curves both within and beyond the turning-point saturations where transitions between branches of the curves occur. Two example problems involving geologic CO 2 storage are simulated with TOUGH2, a multiphase, multicomponent code for flow and transport through geological media. Both non-hysteretic and hysteretic formulations are used, to illustrate the applicability and limitations of non-hysteretic methods. The first application considers leakage of CO 2 from the storage formation to the ground surface, while the second examines the role of heterogeneity within the storage formation

Assessment of oxy-fuel, pre- and post-combustion-based carbon capture for future IGCC plants

International Nuclear Information System (INIS)

Kunze, Christian; Spliethoff, Hartmut

2012-01-01

Highlights: ► Hot gas cleanup is a highly favorable technology for all selected IGCC concepts. ► Proposed high pressure IGCC with membrane reactor enables direct CO 2 condensation. ► IGCC with OTM and carbonate looping enable significant synergy effects. ► Combining IGCC and oxy-fuel is technically challenging but energetically favorable. ► All selected IGCC concepts are able to realize CO 2 capture rates up to 99%. -- Abstract: Environmental damage due to the emission of greenhouse gases from conventional coal-based power plants is a growing concern. Various carbon capture strategies to minimize CO 2 emissions are currently being investigated. Unfortunately, the efficiency drop due to de-carbonization is still significant and the capture rate is limited. Therefore three future hard coal IGCC concepts are assessed here, applying emerging technologies and various carbon capture approaches. The advanced pre-combustion capture concept is based on hot gas clean-up, membrane-enhanced CO conversion and direct CO 2 condensation. The concept reached a net efficiency of 45.1% (LHV), representing an improvement of 6.46% compared to the conventional IGCC base case. The second IGCC concept, based on post-combustion capture via calcination–carbonation loops, hot gas clean-up and oxygen membranes, showed a net efficiency of 45.87% (LHV). The third IGCC concept applies hot gas clean-up and combustion of the unconverted fuel gas using pure oxygen. The oxygen is supplied by an integrated oxygen membrane. The combination of IGCC and oxy-fuel process reached a net efficiency of 45.74% (LHV). In addition to their increased efficiency, all of the concepts showed significantly improved carbon capture rates up to 99%, resulting in virtually carbon-free fossil power plants.

Development of Electro-Microbial Carbon Capture and Conversion Systems

KAUST Repository

Al Rowaihi, Israa

2017-01-01

to fix ca. 800 Gt (gigaton) of CO2 in the planets largest carbon-capture process. Photosynthesis combines light harvesting, charge separation, catalytic water splitting, generation of reduction equivalents (NADH), energy (ATP) production and CO2 fixation

Algae Cultivation for Carbon Capture and Utilization Workshop Summary Report

Energy Technology Data Exchange (ETDEWEB)

None, None

2017-05-01

The Algae Cultivation for Carbon Capture and Utilization Workshop Summary Report summarizes a workshop hosted by the U.S. Department of Energy's Bioenergy Technologies Office on May 23–24, 2017, in Orlando, Florida. The event gathered stakeholder input through facilitated discussions focused on innovative technologies and business strategies for growing algae on waste carbon dioxide resources.

A dynamic mathematical model for packed columns in carbon capture plants

DEFF Research Database (Denmark)

Gaspar, Jozsef; Jørgensen, John Bagterp; Fosbøl, Philip Loldrup

2015-01-01

simulation using monoethanolamine (MEA) and piperazine (PZ) as solvent. MEA is considered as the base-case solvent in the carbon capture business. The effect of changes in the flue gas flow rate and changes in the available steam are investigated to determine their influence on the performance of the capture...

Carbon capture and storage as a corporate technology strategy challenge

International Nuclear Information System (INIS)

Bowen, Frances

2011-01-01

Latest estimates suggest that widespread deployment of carbon capture and storage (CCS) could account for up to one-fifth of the needed global reduction in CO 2 emissions by 2050. Governments are attempting to stimulate investments in CCS technology both directly through subsidizing demonstration projects, and indirectly through developing price incentives in carbon markets. Yet, corporate decision-makers are finding CCS investments challenging. Common explanations for delay in corporate CCS investments include operational concerns such as the high cost of capture technologies, technological uncertainties in integrated CCS systems and underdeveloped regulatory and liability regimes. In this paper, we place corporate CCS adoption decisions within a technology strategy perspective. We diagnose four underlying characteristics of the strategic CCS technology adoption decision that present unusual challenges for decision-makers: such investments are precautionary, sustaining, cumulative and situated. Understanding CCS as a corporate technology strategy challenge can help us move beyond the usual list of operational barriers to CCS and make public policy recommendations to help overcome them. - Research highlights: → Presents a corporate technology strategy perspective on carbon capture and storage (CCS). → CCS technology is precautionary, sustaining, cumulative and situated. → Decision-makers need to look beyond cost and risk as barriers to investment in CCS.

Exploring the role of natural gas power plants with carbon capture and storage as a bridge to a low-carbon future

Science.gov (United States)

Natural gas combined-cycle (NGCC) turbines with carbon capture and storage (CCS) can be a promising technology to reduce CO2 emissions in the electric sector. However, the high cost and energy penalties of current carbon capture devices, as well as methane leakage from natural ga...

Integrated assessment of IGCC power generation technology with carbon capture and storage (CCS)

International Nuclear Information System (INIS)

Cormos, Calin-Cristian

2012-01-01

IGCC (Integrated Gasification Combined Cycle) is a power generation technology in which the solid feedstock is partially oxidized with oxygen and steam to produce syngas. In a conventional IGCC design without carbon capture, the syngas is purified for dust and hydrogen sulphide removal and then it is sent to a CCGT (Combined Cycle Gas Turbine) for power generation. CCS (Carbon capture and storage) technologies are expected to play a significant role in the coming decades for reducing the greenhouse gas emissions. IGCC is one of the power generation technologies having the highest potential to capture CO 2 with low penalties in term of plant energy efficiency, capital and operational costs. This paper investigates the most important techno-economic and environmental indicators (e.g. power output, ancillary consumption, energy efficiency, CW consumption, normalised mass and energy balances and plant construction materials, capital and O and M (operational and maintenance) costs, specific CO 2 emissions, cost of electricity, CO 2 removal and avoidance costs etc.) for IGCC with CCS. Coal-based IGCC cases produce around 400–450 MW net electricity with 90% carbon capture rate. Similar IGCC plants without CCS were presented as references. Future IGCC developments for energy vectors poly-generation were also presented. -- Highlights: ► Techno-economical evaluations of coal-based IGCC power generation with CCS. ► Model development for capital, O and M, CO 2 capture costs and cash flow estimations. ► Technical and economic investigations of key plant design characteristics. ► Evaluations of carbon capture options for IGCC power generation technology.

Technological learning for carbon capture and sequestration technologies

International Nuclear Information System (INIS)

Riahi, Keywan; Rubin, Edward S.; Taylor, Margaret R.; Schrattenholzer, Leo; Hounshell, David

2004-01-01

This paper analyzes potentials of carbon capture and sequestration technologies (CCT) in a set of long-term energy-economic-environmental scenarios based on alternative assumptions for technological progress of CCT. In order to get a reasonable guide to future technological progress in managing CO 2 emissions, we review past experience in controlling sulfur dioxide (SO 2 ) emissions from power plants. By doing so, we quantify a 'learning curve' for CCT, which describes the relationship between the improvement of costs due to accumulation of experience in CCT construction. We incorporate the learning curve into the energy-modeling framework MESSAGE-MACRO and develop greenhouse gas emissions scenarios of economic, demographic, and energy demand development, where alternative policy cases lead to the stabilization of atmospheric CO 2 concentrations at 550 parts per million by volume (ppmv) by the end of the 21st century. We quantify three types of contributors to the carbon emissions mitigation: (1) demand reductions due to the increased price of energy, (2) fuel switching primarily away from coal, and (3) carbon capture and sequestration from fossil fuels. Due to the assumed technological learning, costs of the emissions reduction for CCT drop rapidly and in parallel with the massive introduction of CCT on the global scale. Compared to scenarios based on static cost assumptions for CCT, the contribution of carbon sequestration is about 50% higher in the case of learning, resulting in cumulative sequestration of CO 2 ranging from 150 to 250 billion (10 9 ) tons with carbon during the 21st century. Also, carbon values (tax) across scenarios (to meet the 550 ppmv carbon concentration constraint) are between 2% and 10% lower in the case of learning for CCT by 2100. The results illustrate that assumptions on technological change are a critical determinant of future characteristics of the energy system, indicating the importance of long-term technology policies in

Trade-off in emissions of acid gas pollutants and of carbon dioxide in fossil fuel power plants with carbon capture

International Nuclear Information System (INIS)

Tzimas, Evangelos; Mercier, Arnaud; Cormos, Calin-Cristian; Peteves, Stathis D.

2007-01-01

This paper investigates the impact of capture of carbon dioxide (CO 2 ) from fossil fuel power plants on the emissions of nitrogen oxides (NO X ) and sulphur oxides (SO X ), which are acid gas pollutants. This was done by estimating the emissions of these chemical compounds from natural gas combined cycle and pulverized coal plants, equipped with post-combustion carbon capture technology for the removal of CO 2 from their flue gases, and comparing them with the emissions of similar plants without CO 2 capture. The capture of CO 2 is not likely to increase the emissions of acid gas pollutants from individual power plants; on the contrary, some NO X and SO X will also be removed during the capture of CO 2 . The large-scale implementation of carbon capture is however likely to increase the emission levels of NO X from the power sector due to the reduced efficiency of power plants equipped with capture technologies. Furthermore, SO X emissions from coal plants should be decreased to avoid significant losses of the chemicals that are used to capture CO 2 . The increase in the quantity of NO X emissions will be however low, estimated at 5% for the natural gas power plant park and 24% for the coal plants, while the emissions of SO X from coal fired plants will be reduced by as much as 99% when at least 80% of the CO 2 generated will be captured

Carbon Capture and Storage and the London Protocol

Energy Technology Data Exchange (ETDEWEB)

NONE

2011-07-01

The International Energy Agency (IEA) estimates that 100 Carbon Capture and Storage (CCS) projects will be required by 2020 and over 3000 by 2050 if CCS is to contribute fully to the least-cost technology portfolio for CO2 mitigation. For CCS to reach its emissions reduction potential, the 2009 IEA publication Technology Roadmap: Carbon Capture and Storage recommends that international legal obstacles associated with global CCS deployment be removed by 2012 -- including the prohibition on transboundary CO2 transfer under the London Protocol. The London Protocol was amended by contracting parties in 2009 to allow for cross-border transportation of CO2 for sub-seabed storage, but the amendment must be ratified by two-thirds of contracting parties to enter into force. It is unlikely that this will occur in the near term; this working paper therefore outlines options that may be available to contracting parties under international law to address the barrier to deployment presented by Article 6, pending formal entry into force of the 2009 amendment.

Biorefineries of carbon dioxide: From carbon capture and storage (CCS) to bioenergies production.

Science.gov (United States)

Cheah, Wai Yan; Ling, Tau Chuan; Juan, Joon Ching; Lee, Duu-Jong; Chang, Jo-Shu; Show, Pau Loke

2016-09-01

Greenhouse gas emissions have several adverse environmental effects, like pollution and climate change. Currently applied carbon capture and storage (CCS) methods are not cost effective and have not been proven safe for long term sequestration. Another attractive approach is CO2 valorization, whereby CO2 can be captured in the form of biomass via photosynthesis and is subsequently converted into various form of bioenergy. This article summarizes the current carbon sequestration and utilization technologies, while emphasizing the value of bioconversion of CO2. In particular, CO2 sequestration by terrestrial plants, microalgae and other microorganisms are discussed. Prospects and challenges for CO2 conversion are addressed. The aim of this review is to provide comprehensive knowledge and updated information on the current advances in biological CO2 sequestration and valorization, which are essential if this approach is to achieve environmental sustainability and economic feasibility. Copyright © 2016 Elsevier Ltd. All rights reserved.

Production of biodiesel from microalgae through biological carbon capture: a review.

Science.gov (United States)

Mondal, Madhumanti; Goswami, Shrayanti; Ghosh, Ashmita; Oinam, Gunapati; Tiwari, O N; Das, Papita; Gayen, K; Mandal, M K; Halder, G N

2017-06-01

Gradual increase in concentration of carbon dioxide (CO 2 ) in the atmosphere due to the various anthropogenic interventions leading to significant alteration in the global carbon cycle has been a subject of worldwide attention and matter of potential research over the last few decades. In these alarming scenario microalgae seems to be an attractive medium for capturing the excess CO 2 present in the atmosphere generated from different sources such as power plants, automobiles, volcanic eruption, decomposition of organic matters and forest fires. This captured CO 2 through microalgae could be used as potential carbon source to produce lipids for the generation of biofuel for replacing petroleum-derived transport fuel without affecting the supply of food and crops. This comprehensive review strives to provide a systematic account of recent developments in the field of biological carbon capture through microalgae for its utilization towards the generation of biodiesel highlighting the significance of certain key parameters such as selection of efficient strain, microalgal metabolism, cultivation systems (open and closed) and biomass production along with the national and international biodiesel specifications and properties. The potential use of photobioreactors for biodiesel production under the influence of various factors viz., light intensity, pH, time, temperature, CO 2 concentration and flow rate has been discussed. The review also provides an economic overview and future outlook on biodiesel production from microalgae.

Elemental mercury vapor capture by powdered activated carbon in a fluidized bed reactor

Energy Technology Data Exchange (ETDEWEB)

Fabrizio Scala; Riccardo Chirone; Amedeo Lancia [Istituto di Ricerche sulla Combustione - CNR, Napoli (Italy)

2011-06-15

A bubbling fluidized bed of inert material was used to increase the activated carbon residence time in the reaction zone and to improve its performance for mercury vapor capture. Elemental mercury capture experiments were conducted at 100{sup o}C in a purposely designed 65 mm ID lab-scale pyrex reactor, that could be operated both in the fluidized bed and in the entrained bed configurations. Commercial powdered activated carbon was pneumatically injected in the reactor and mercury concentration at the outlet was monitored continuously. Experiments were carried out at different inert particle sizes, bed masses, fluidization velocities and carbon feed rates. Experimental results showed that the presence of a bubbling fluidized bed led to an increase of the mercury capture efficiency and, in turn, of the activated carbon utilization. This was explained by the enhanced activated carbon loading and gas-solid contact time that establishes in the reaction zone, because of the large surface area available for activated carbon adhesion/deposition in the fluidized bed. Transient mercury concentration profiles at the bed outlet during the runs were used to discriminate between the controlling phenomena in the process. Experimental data have been analyzed in the light of a phenomenological framework that takes into account the presence of both free and adhered carbon in the reactor as well as mercury saturation of the adsorbent. 14 refs., 7 figs.

On the limits of CO2 capture capacity of carbons

OpenAIRE

Fernández Martín, Claudia; González Plaza, Marta; Pis Martínez, José Juan; Rubiera González, Fernando; Pevida García, Covadonga; Álvarez Centeno, Teresa

2010-01-01

This study shows that standard techniques used for carbons characterization, such as physical adsorption of CO2 at 273 K and N2 at 77 K, can be used to assess, with a good accuracy, the maximum capacity of carbons to capture CO2 under post- and pre-combustion conditions. The analysis of the corresponding adsorption isotherms, within the general theoretical framework of Dubinin's theory, leads to the values of the micropore volume, Wo, and the characteristic energy, Eo, of the carbons, which p...

The Role of Natural Gas Power Plants with Carbon Capture and Storage in a Low-Carbon Future

Science.gov (United States)

Natural gas combined-cycle (NGCC) turbines with carbon capture and storage (CCS) are a promising technology for reducing carbon dioxide (CO2) emissions in the electric sector. However, the high cost and efficiency penalties associated with CCS, as well as methane leakage from nat...

Incentives for early adoption of carbon capture technology

International Nuclear Information System (INIS)

Comello, Stephen; Reichelstein, Stefan

2014-01-01

We analyze a policy proposal for regulating the next generation of baseload electricity generation facilities in the United States. The cornerstone of this regulation is a (hypothetical) EPA mandate for an emission standard of 80 kg of CO 2 per MWh of electricity generated. The mandate would go into effect at the end of 2027 for all power generating facilities that come into operation after 2017. Fossil-fuel power plants could meet the standard by capturing between 80 and 90% of their current CO 2 emissions. While the initial cost of complying with this standard is relatively high for first-of-a-kind facilities, learning effects are projected to reduce this cost substantially by the end of 2027, provided new facilities consistently adopt carbon capture technology in the intervening years. We identify a combination of investment- and production tax credits that provide the required incentives for new facilities to be willing to comply with the standard ahead of the mandate. Due to the anticipated learning effects, the incremental cost associated with the stricter emission limit is projected to about 1.2¢ per kWh of electricity in the long run. - Highlights: • Study the cost effects of a CO 2 emission standard for natural gas power plants. • The standard requires the deployment of carbon capture technology. • Future compliance costs are reduced through learning effects. • Identify tax incentives that induce early technology adoption. • Early adoption results in relatively modest electricity cost increases

Microporous metal-organic framework with potential for carbon dioxide capture at ambient conditions

NARCIS (Netherlands)

Xiang, S.C.; He, Y.; Zhang, Z.; Wu, H.; Zhou, W.; Krishna, R.; Chen, B.

2012-01-01

Carbon dioxide capture and separation are important industrial processes that allow the use of carbon dioxide for the production of a range of chemical products and materials, and to minimize the effects of carbon dioxide emission. Porous metal-organic frameworks are promising materials to achieve

Carbon Capture and Storage Legal and Regulatory Review. Edition 3

Energy Technology Data Exchange (ETDEWEB)

NONE

2012-07-01

The International Energy Agency (IEA) considers carbon capture and storage (CCS) a crucial part of worldwide efforts to limit global warming by reducing greenhouse-gas emissions. The IEA estimates that emissions can be reduced to a level consistent with a 2°C global temperature increase through the broad deployment of low-carbon energy technologies – and that CCS would contribute about one-fifth of emission reductions in this scenario. Achieving this level of deployment will require that regulatory frameworks – or rather a lack thereof – do not unnecessarily impede environmentally safe demonstration and deployment of CCS, so in October 2010 the IEA launched the IEA Carbon Capture and Storage Legal and Regulatory Review. The CCS Review is a regular review of CCS regulatory progress worldwide. Produced annually, it collates contributions by national and regional governments, as well as leading organisations engaged in CCS regulatory activities, to provide a knowledge-sharing forum to support CCS framework development. Each two page contribution provides a short summary of recent and anticipated CCS regulatory developments and highlights a particular, pre-nominated regulatory theme. To introduce each edition, the IEA provides a brief analysis of key advances and trends, based on the contributions submitted. The theme for this third edition is stakeholder engagement in the development of CO2 storage projects. Other issues addressed include: regulating CO2-EOR, CCS and CO2-EOR for storage; CCS incentive policy; key, substantive issues being addressed by jurisdictions taking steps to finalise CCS regulatory framework development; and CCS legal and regulatory developments in the context of the Clean Energy Ministerial Carbon Capture, Use and Storage Action Group.

Method and system for capturing carbon dioxide and/or sulfur dioxide from gas stream

Science.gov (United States)

Chang, Shih-Ger; Li, Yang; Zhao, Xinglei

2014-07-08

The present invention provides a system for capturing CO.sub.2 and/or SO.sub.2, comprising: (a) a CO.sub.2 and/or SO.sub.2 absorber comprising an amine and/or amino acid salt capable of absorbing the CO.sub.2 and/or SO.sub.2 to produce a CO.sub.2- and/or SO.sub.2-containing solution; (b) an amine regenerator to regenerate the amine and/or amino acid salt; and, when the system captures CO.sub.2, (c) an alkali metal carbonate regenerator comprising an ammonium catalyst capable catalyzing the aqueous alkali metal bicarbonate into the alkali metal carbonate and CO.sub.2 gas. The present invention also provides for a system for capturing SO.sub.2, comprising: (a) a SO.sub.2 absorber comprising aqueous alkali metal carbonate, wherein the alkali metal carbonate is capable of absorbing the SO.sub.2 to produce an alkali metal sulfite/sulfate precipitate and CO.sub.2.

Transport of Perfluorocarbon Tracers in the Cranfield Geological Carbon Sequestration Project

Science.gov (United States)

Moortgat, J.; Soltanian, M. R.; Amooie, M. A.; Cole, D. R.; Graham, D. E.; Pfiffner, S. M.; Phelps, T.

2017-12-01

A field-scale carbon dioxide (CO2) injection pilot project was conducted by the Southeast Regional Sequestration Partnership (SECARB) at Cranfield, Mississippi. Two associated campaigns in 2009 and 2010 were carried out to co-inject perfluorocarbon tracers (PFTs) and sulfur hexafluoride (SF6) with CO2. Tracers in gas samples from two observation wells were analyzed to construct breakthrough curves. We present the compiled field data as well as detailed numerical modeling of the flow and transport of CO2, brine, and introduced tracers. A high-resolution static model of the formation geology in the Detailed Area Study (DAS) was used in order to capture the impact of connected flow pathways created by fluvial channels on breakthrough curves and breakthrough times of PFTs and SF6 tracers. We use the cubic-plus-association (CPA) equation of state, which takes into account the polar nature of water molecules, to describe the phase behavior of CO2-brine-tracer mixtures. We show how the combination of multiple tracer injection pulses with detailed numerical simulations provide a powerful tool in constraining both formation properties and how complex flow pathways develop over time.

Unravelling the Contested Nature of Carbon Capture and Storage

NARCIS (Netherlands)

van Egmond, Sander

2016-01-01

Our climate is changing. Carbon Capture and Storage (CCS) has been identified as an important technology to reduce CO2 emissions in order to avoid dangerous climate change. The implementation of CCS is however slow and CCS is publicly contested. This thesis focuses on the debate on this technology.

Carbon Capture and Storage: Progress and Next Steps

Energy Technology Data Exchange (ETDEWEB)

NONE

2010-07-01

Two years after the G8 leaders commitment to the broad deployment of carbon capture and storage (CCS) by 2020, significant progress has been made towards commercialisation of CCS technologies. Yet the 2008 Hokkaido G8 recommendation to launch 20 large-scale CCS demonstration projects by 2010 remains a challenge and will require that governments and industry accelerate the pace toward achieving this critical goal. This is one of the main findings of a new report by the International Energy Agency (IEA), the Carbon Sequestration Leadership Forum (CSLF), and the Global CCS Institute, to be presented to G8 leaders at their June Summit in Muskoka, Canada.

Integrating Algae with Bioenergy Carbon Capture and Storage (ABECCS) Increases Sustainability

Science.gov (United States)

Beal, Colin M.; Archibald, Ian; Huntley, Mark E.; Greene, Charles H.; Johnson, Zackary I.

2018-03-01

Bioenergy carbon capture and storage (BECCS) has been proposed to reduce atmospheric CO2 concentrations, but concerns remain about competition for arable land and freshwater. The synergistic integration of algae production, which does not require arable land or freshwater, with BECCS (called "ABECCS") can reduce CO2 emissions without competing with agriculture. This study presents a technoeconomic and life-cycle assessment for colocating a 121-ha algae facility with a 2,680-ha eucalyptus forest for BECCS. The eucalyptus biomass fuels combined heat and power (CHP) generation with subsequent amine-based carbon capture and storage (CCS). A portion of the captured CO2 is used for growing algae and the remainder is sequestered. Biomass combustion supplies CO2, heat, and electricity, thus increasing the range of sites suitable for algae cultivation. Economic, energetic, and environmental impacts are considered. The system yields as much protein as soybeans while generating 61.5 TJ of electricity and sequestering 29,600 t of CO2 per year. More energy is generated than consumed and the freshwater footprint is roughly equal to that for soybeans. Financial break-even is achieved for product value combinations that include 1) algal biomass sold for 1,400/t (fishmeal replacement) with a 68/t carbon credit and 2) algal biomass sold for 600/t (soymeal replacement) with a 278/t carbon credit. Sensitivity analysis shows significant reductions to the cost of carbon sequestration are possible. The ABECCS system represents a unique technology for negative emissions without reducing protein production or increasing water demand, and should therefore be included in the suite of technologies being considered to address global sustainability.

Mercury capture by selected Bulgarian fly ashes: Influence of coal rank and fly ash carbon pore structure on capture efficiency

Science.gov (United States)

Kostova, I.J.; Hower, J.C.; Mastalerz, Maria; Vassilev, S.V.

2011-01-01

Mercury capture by fly ash C was investigated at five lignite- and subbituminous-coal-burning Bulgarian power plants (Republika, Bobov Dol, Maritza East 2, Maritza East 3, and Sliven). Although the C content of the ashes is low, never exceeding 1.6%, the Hg capture on a unit C basis demonstrates that the low-rank-coal-derived fly ash carbons are more efficient in capturing Hg than fly ash carbons from bituminous-fired power plants. While some low-C and low-Hg fly ashes do not reveal any trends of Hg versus C, the 2nd and, in particular, the 3rd electrostatic precipitator (ESP) rows at the Republika power plant do have sufficient fly ash C range and experience flue gas sufficiently cool to capture measurable amounts of Hg. The Republika 3rd ESP row exhibits an increase in Hg with increasing C, as observed in other power plants, for example, in Kentucky power plants burning Appalachian-sourced bituminous coals. Mercury/C decreases with an increase in fly ash C, suggesting that some of the C is isolated from the flue gas stream and does not contribute to Hg capture. Mercury capture increases with an increase in Brunauer-Emmett-Teller (BET) surface area and micropore surface area. The differences in Hg capture between the Bulgarian plants burning low-rank coal and high volatile bituminous-fed Kentucky power plants suggests that the variations in C forms resulting from the combustion of the different ranks also influence the efficiency of Hg capture. ?? 2010 Elsevier Ltd.

Mercury capture by selected Bulgarian fly ashes: Influence of coal rank and fly ash carbon pore structure on capture efficiency

Energy Technology Data Exchange (ETDEWEB)

Kostova, I.J.; Hower, J.C.; Mastalerz, M.; Vassilev, S.V. [University of Kentucky, Lexington, KY (United States). Center of Applied Energy Research

2011-01-15

Mercury capture by fly ash C was investigated at five lignite- and subbituminous-coal-burning Bulgarian power plants (Republika, Bobov Dol, Maritza East 2, Maritza East 3, and Sliven). Although the C content of the ashes is low, never exceeding 1.6%, the Hg capture on a unit C basis demonstrates that the low-rank-coal-derived fly ash carbons are more efficient in capturing Hg than fly ash carbons from bituminous-fired power plants. While some low-C and low-Hg fly ashes do not reveal any trends of Hg versus C, the 2nd and, in particular, the 3rd electrostatic precipitator (ESP) rows at the Republika power plant do have sufficient fly ash C range and experience flue gas sufficiently cool to capture measurable amounts of Hg. The Republika 3rd ESP row exhibits an increase in Hg with increasing C, as observed in other power plants, for example, in Kentucky power plants burning Appalachian-sourced bituminous coals. Mercury/C decreases with an increase in fly ash C, suggesting that some of the C is isolated from the flue gas stream and does not contribute to Hg capture. Mercury capture increases with an increase in Brunauer-Emmett-Teller (BET) surface area and micropore surface area. The differences in Hg capture between the Bulgarian plants burning low-rank coal and high volatile bituminous-fed Kentucky power plants suggests that the variations in C forms resulting from the combustion of the different ranks also influence the efficiency of Hg capture.

An Integrated, Low Temperature Process to Capture and Sequester Carbon Dioxide from Industrial Emissions

Science.gov (United States)

Wendlandt, R. F.; Foremski, J. J.

2013-12-01

Laboratory experiments show that it is possible to integrate (1) the chemistry of serpentine dissolution, (2) capture of CO2 gas from the combustion of natural gas and coal-fired power plants using aqueous amine-based solvents, (3) long-term CO2 sequestration via solid phase carbonate precipitation, and (4) capture solvent regeneration with acid recycling in a single, continuous process. In our process, magnesium is released from serpentine at 300°C via heat treatment with ammonium sulfate salts or at temperatures as low as 50°C via reaction with sulfuric acid. We have also demonstrated that various solid carbonate phases can be precipitated directly from aqueous amine-based (NH3, MEA, DMEA) CO2 capture solvent solutions at room temperature. Direct precipitation from the capture solvent enables regenerating CO2 capture solvent without the need for heat and without the need to compress the CO2 off gas. We propose that known low-temperature electrochemical methods can be integrated with this process to regenerate the aqueous amine capture solvent and recycle acid for dissolution of magnesium-bearing mineral feedstocks and magnesium release. Although the direct precipitation of magnesite at ambient conditions remains elusive, experimental results demonstrate that at temperatures ranging from 20°C to 60°C, either nesquehonite Mg(HCO3)(OH)●2H2O or a double salt with the formula [NH4]2Mg(CO3)2●4H2O or an amorphous magnesium carbonate precipitate directly from the capture solvent. These phases are less desirable for CO2 sequestration than magnesite because they potentially remove constituents (water, ammonia) from the reaction system, reducing the overall efficiency of the sequestration process. Accordingly, the integrated process can be accomplished with minimal energy consumption and loss of CO2 capture and acid solvents, and a net generation of 1 to 4 moles of H2O/6 moles of CO2 sequestered (depending on the solid carbonate precipitate and amount of produced H2

International Symposium on Site Characterization for CO2Geological Storage

Energy Technology Data Exchange (ETDEWEB)

Tsang, Chin-Fu

2006-02-23

Several technological options have been proposed to stabilize atmospheric concentrations of CO{sub 2}. One proposed remedy is to separate and capture CO{sub 2} from fossil-fuel power plants and other stationary industrial sources and to inject the CO{sub 2} into deep subsurface formations for long-term storage and sequestration. Characterization of geologic formations for sequestration of large quantities of CO{sub 2} needs to be carefully considered to ensure that sites are suitable for long-term storage and that there will be no adverse impacts to human health or the environment. The Intergovernmental Panel on Climate Change (IPCC) Special Report on Carbon Dioxide Capture and Storage (Final Draft, October 2005) states that ''Site characterization, selection and performance prediction are crucial for successful geological storage. Before selecting a site, the geological setting must be characterized to determine if the overlying cap rock will provide an effective seal, if there is a sufficiently voluminous and permeable storage formation, and whether any abandoned or active wells will compromise the integrity of the seal. Moreover, the availability of good site characterization data is critical for the reliability of models''. This International Symposium on Site Characterization for CO{sub 2} Geological Storage (CO2SC) addresses the particular issue of site characterization and site selection related to the geologic storage of carbon dioxide. Presentations and discussions cover the various aspects associated with characterization and selection of potential CO{sub 2} storage sites, with emphasis on advances in process understanding, development of measurement methods, identification of key site features and parameters, site characterization strategies, and case studies.

Modelling of tetrahydrofuran promoted gas hydrate systems for carbon dioxide capture processes

DEFF Research Database (Denmark)

Herslund, Peter Jørgensen; Thomsen, Kaj; Abildskov, Jens

2014-01-01

A thermodynamic study of a novel gas hydrate based CO2 capture process is presented.•Model predicts this process unsuitable for CO2 capture from power station flue gases. A thermodynamic modelling study of both fluid phase behaviour and hydrate phase behaviour is presented for the quaternary system...... of water, tetrahydrofuran, carbon dioxide and nitrogen. The applied model incorporates the Cubic-Plus-Association (CPA) equation of state for the fluid phase description and the van der Waals-Platteeuw hydrate model for the solid (hydrate) phase. Six binary pairs are studied for their fluid phase behaviour...... accurate descriptions of both fluid- and hydrate phase equilibria in the studied system and its subsystems. The developed model is applied to simulate two simplified, gas hydrate-based processes for post-combustion carbon dioxide capture from power station flue gases. The first process, an unpromoted...

CO{sub 2} capture using some fly ash-derived carbon materials

Energy Technology Data Exchange (ETDEWEB)

A. Arenillas; K.M. Smith; T.C. Drage; C.E. Snape [University of Nottingham, Nottingham (United Kingdom). Nottingham Fuel and Energy Centre, School of Chemical, Environmental and Mining Engineering

2005-12-01

Adsorption is considered to be one of the more promising technologies for capturing CO{sub 2} from flue gases. For post-combustion capture, the success of such an approach is however dependent on the development of an adsorbent that can operate competitively at relatively high temperatures. In this work, low cost carbon materials derived from fly ash, are presented as effective CO{sub 2} sorbents through impregnation these with organic bases, for example, polyethylenimine aided by polyethylene glycol. The results show that for samples derived from a fly ash carbon concentrate, the CO{sub 2} adsorption capacities were relatively high (up to 4.5 wt%) especially at high temperatures (75{sup o}C), where commercial active carbons relying on physi-sorption have low capacities. The addition of PEG improves the adsorption capacity and reduces the time taken for the sample to reach the equilibrium. No CO{sub 2} seems to remain after desorption, suggesting that the process is fully reversible. 24 refs., 6 figs., 2 tabs.

Geochemical Impacts to Groundwater from Geologic Carbon Sequestration: Controls on pH and Inorganic Carbon Concentrations from Reaction Path and Kinetic Modeling

Science.gov (United States)

Geologic carbon sequestration has the potential to cause long-term reductions in global emissions of carbon dioxide to the atmosphere. Safe and effective application of carbon sequestration technology requires an understanding of the potential risks to the quality of underground...

Environmental Externalities of Geological Carbon Sequestration Effects on Energy Scenarios

International Nuclear Information System (INIS)

Smekens, K.; Van der Zwaan, B.

2004-03-01

Geological carbon sequestration seems one of the promising options to address, in the near term, the global problem of climate change, since carbon sequestration technologies are in principle available today and their costs are expected to be affordable. Whereas extensive technological and economic feasibility studies rightly point out the large potential of this 'clean fossil fuel' option, relatively little attention has been paid so far to the detrimental environmental externalities that the sequestering of CO2 underground could entail. This paper assesses what the relevance might be of including these external effects in long-term energy planning and scenario analyses. Our main conclusion is that, while these effects are generally likely to be relatively small, carbon sequestration externalities do matter and influence the nature of future world energy supply and consumption. More importantly, since geological carbon storage (depending on the method employed) may in some cases have substantial external impacts, in terms of both environmental damage and health risks, it is recommended that extensive studies are performed to quantify these effects. This article addresses three main questions: (1) What may energy supply look like if one accounts for large-scale CO2 sequestration in the construction of long-term energy and climate change scenarios; (2) Suppose one hypothesizes a quantification of the external environmental costs of CO2 sequestration, how do then these supposed costs affect the evolution of the energy system during the 21st century; (3) Does it matter for these scenarios whether carbon sequestration damage costs are charged directly to consumers or, instead, to electricity producers?

Final Scientific/Technical Report Carbon Capture and Storage Training Northwest - CCSTNW

Energy Technology Data Exchange (ETDEWEB)

Workman, James

2013-09-30

This report details the activities of the Carbon Capture and Storage Training Northwest (CCSTNW) program 2009 to 2013. The CCSTNW created, implemented, and provided Carbon Capture and Storage (CCS) training over the period of the program. With the assistance of an expert advisory board, CCSTNW created curriculum and conducted three short courses, more than three lectures, two symposiums, and a final conference. The program was conducted in five phases; 1) organization, gap analysis, and form advisory board; 2) develop list serves, website, and tech alerts; 3) training needs survey; 4) conduct lectures, courses, symposiums, and a conference; 5) evaluation surveys and course evaluations. This program was conducted jointly by Environmental Outreach and Stewardship Alliance (dba. Northwest Environmental Training Center – NWETC) and Pacific Northwest National Laboratories (PNNL).

Measurement and Modelling of the Piperazine Potassium Carbonate Solutions for CO2 Capture

DEFF Research Database (Denmark)

Fosbøl, Philip Loldrup; Thomsen, Kaj; Waseem Arshad, Muhammad

The climate is in a critical state due to the impact of pollution by CO2 and similar greenhouse gasses. Action needs to be taken in order reduce the emission of harmful components. CO2 capture is one process to help the world population back on track in order to return to normal condition...... with the purpose of simulating the CO2 capture process. This involves equilibrium studies on physical properties in the activated carbonate solvent. Energy consumption while applying the promoted carbonate solutions using piperazine is given in overview....

Combustion systems and power plants incorporating parallel carbon dioxide capture and sweep-based membrane separation units to remove carbon dioxide from combustion gases

Science.gov (United States)

Wijmans, Johannes G [Menlo Park, CA; Merkel, Timothy C [Menlo Park, CA; Baker, Richard W [Palo Alto, CA

2011-10-11

Disclosed herein are combustion systems and power plants that incorporate sweep-based membrane separation units to remove carbon dioxide from combustion gases. In its most basic embodiment, the invention is a combustion system that includes three discrete units: a combustion unit, a carbon dioxide capture unit, and a sweep-based membrane separation unit. In a preferred embodiment, the invention is a power plant including a combustion unit, a power generation system, a carbon dioxide capture unit, and a sweep-based membrane separation unit. In both of these embodiments, the carbon dioxide capture unit and the sweep-based membrane separation unit are configured to be operated in parallel, by which we mean that each unit is adapted to receive exhaust gases from the combustion unit without such gases first passing through the other unit.

Location of geologic structures from interpretation of ERTS-1 imagery, Carbon County, Wyoming

Science.gov (United States)

Marrs, R. W.; Barton, R.

1974-01-01

The author has identified the following significant results. Possible geologic structures in the basin sediments of Carbon County and vicinity were located by interpretation of ERTS-1 imagery. These same structures are not evident on existing conventional geologic maps of the area. Subsequent field checks confirmed much of the geologic interpretation, but revealed that two apparent closed structures identified on the ERTS-1 imagery were actually topographic pseudostructures in flat or homoclinal sediments. Stereoscopic coverage (where available) allows the interpreter to avoid such misinterpretations.

Climate Change Mitigation Technologies: the Siemens Roadmap to Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

Voges, K.

2007-07-01

A full range of technology options will have to be deployed until 2025 to get the global CO{sub 2} emissions on a 550 ppm stabilization track. The focus of the paper will be on Carbon Capture and Storage (CCS) as an indispensable part of a carbon constrained energy infrastructure. In CCS our main long term focus is clearly on coal based processes. For Greenfield applications Siemens is prioritizing IGCC based pre-combustion capture. Post-combustion capture is pursued for steam power plant retrofit. (a) IGCC with pre-combustion capture: A first F-class based demonstration plant could be available until 2014. The roadmap addresses gasifier scale up, hydrogen burner and turbine development and integration issues. Beyond that a bundle of further efficiency improvement measures will further enhance efficiency and economic competitiveness. (b) Post-combustion capture: The development aims at optimizing existing solvents or developing new ones and integrating the complete unit with its mass and heat interchange system into the power plant. (c) CO{sub 2} Compressors: For efficiency and operating flexibility reasons Siemens Power Generation prefers gear-type compressors instead of single shaft compressors. The improvement of maintainability and the reduced number of stages or corrosion protection are issues addressed in current R and D activities. (auth)

Materials design for electrocatalytic carbon capture

Directory of Open Access Journals (Sweden)

Xin Tan

2016-05-01

Full Text Available We discuss our philosophy for implementation of the Materials Genome Initiative through an integrated materials design strategy, exemplified here in the context of electrocatalytic capture and separation of CO2 gas. We identify for a group of 1:1 X–N graphene analogue materials that electro-responsive switchable CO2 binding behavior correlates with a change in the preferred binding site from N to the adjacent X atom as negative charge is introduced into the system. A reconsideration of conductive N-doped graphene yields the discovery that the N-dopant is able to induce electrocatalytic binding of multiple CO2 molecules at the adjacent carbon sites.

Developments since 2005 in understanding potential environmental impacts of CO2 leakage from geological storage

NARCIS (Netherlands)

Jones, D.G.; Beaubien, S.E.; Blackford, J.C.; Foekema, E.M.; Lions, J.; Vittor, de C.; West, J.M.; Widdicombe, S.; Hauton, C.; Queiros, A.M.

2015-01-01

This paper reviews research into the potential environmental impacts of leakage from geological storage of CO2 since the publication of the IPCC Special Report on Carbon Dioxide Capture and Storage in 2005. Possible impacts are considered on onshore (including drinking water aquifers) and offshore

Carbon capture and storage (CCS) in a civil legal point of view; CO{sub 2}-Abscheidung und -Ablagerung (Carbon Capture and Storage - CCS) in zivilrechtlicher Sicht

Energy Technology Data Exchange (ETDEWEB)

Gast, Ina Carolin

2012-11-01

The author of the book under consideration reports on the possibilities of the German environmental private law in order to address the risks of carbon capture and storage. The focus of this book is concerned with the examination of defense claims, compensation claims and claims for damages of the persons concerned, if activities or plants for carbon capture and storage cause damages at the legal assets. In addition to the civil defense claims and compensation claims from paragraph 1004 sect. 1 of the German civil code (BGB) and paragraph 906 sect. 2 sentence 2 BGB also claims under public law concerning the respective interests of neighbours from paragraph 75 sect. 2 sentence 2 to 4 VwVfG (Law on Administrative Procedure) also shall be included. In addition to this, the author reports on the claims for compensation of tort law and various situations of the strict liability. In particular, the new paragraph 29 of the draft of the carbon dioxide storage law is considered which creates a special strict liability for this novel technology.

Calcifying Cyanobacteria - The potential of biomineralization for Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

Jansson, Christer G; Northen, Trent

2010-03-26

Employment of cyanobacteria in biomineralization of carbon dioxide by calcium carbonate precipitation offers novel and self-sustaining strategies for point-source carbon capture and sequestration. Although details of this process remain to be elucidated, a carbon-concentrating mechanism, and chemical reactions in exopolysaccharide or proteinaceous surface layers are assumed to be of crucial importance. Cyanobacteria can utilize solar energy through photosynthesis to convert carbon dioxide to recalcitrant calcium carbonate. Calcium can be derived from sources such as gypsum or industrial brine. A better understanding of the biochemical and genetic mechanisms that carry out and regulate cynaobacterial biomineralization should put us in a position where we can further optimize these steps by exploiting the powerful techniques of genetic engineering, directed evolution, and biomimetics.

Multi-fuel multi-product operation of IGCC power plants with carbon capture and storage (CCS)

International Nuclear Information System (INIS)

Cormos, Ana-Maria; Dinca, Cristian; Cormos, Calin-Cristian

2015-01-01

This paper investigates multi-fuel multi-product operation of IGCC plants with carbon capture and storage (CCS). The investigated plant designs co-process coal with different sorts of biomass (e.g. sawdust) and solid wastes, through gasification, leading to different decarbonised energy vectors (power, hydrogen, heat, substitute natural gas etc.) simultaneous with carbon capture. Co-gasification of coal with different renewable energy sources coupled with carbon capture will pave the way towards zero emissions power plants. The energy conversions investigated in the paper were simulated using commercial process flow modelling package (ChemCAD) in order to produce mass and energy balances necessary for the proposed evaluation. As illustrative cases, hydrogen and power co-generation and Fischer–Tropsch fuel synthesis (both with carbon capture), were presented. The case studies investigated in the paper produce a flexible ratio between power and hydrogen (in the range of 400–600 MW net electricity and 0–200 MW th hydrogen considering the lower heating value) with at least 90% carbon capture rate. Special emphasis were given to fuel selection criteria for optimisation of gasification performances (fuel blending), to the selection criteria for gasification reactor in a multi-fuel multi-product operation scenario, modelling and simulation of whole process, to thermal and power integration of processes, flexibility analysis of the energy conversion processes, in-depth techno-economic and environmental assessment etc. - Highlights: • Assessment of IGCC-based energy vectors poly-generation systems with CCS. • Optimisation of gasification performances and CO 2 emissions by fuel blending. • Multi-fuel multi-product operation of gasification plants

Carbon Capture and Utilization in the Industrial Sector.

Science.gov (United States)

Psarras, Peter C; Comello, Stephen; Bains, Praveen; Charoensawadpong, Panunya; Reichelstein, Stefan; Wilcox, Jennifer

2017-10-03

The fabrication and manufacturing processes of industrial commodities such as iron, glass, and cement are carbon-intensive, accounting for 23% of global CO 2 emissions. As a climate mitigation strategy, CO 2 capture from flue gases of industrial processes-much like that of the power sector-has not experienced wide adoption given its high associated costs. However, some industrial processes with relatively high CO 2 flue concentration may be viable candidates to cost-competitively supply CO 2 for utilization purposes (e.g., polymer manufacturing, etc.). This work develops a methodology that determines the levelized cost ($/tCO 2 ) of separating, compressing, and transporting carbon dioxide. A top-down model determines the cost of separating and compressing CO 2 across 18 industrial processes. Further, the study calculates the cost of transporting CO 2 via pipeline and tanker truck to appropriately paired sinks using a bottom-up cost model and geo-referencing approach. The results show that truck transportation is generally the low-cost alternative given the relatively small volumes (ca. 100 kt CO 2 /a). We apply our methodology to a regional case study in Pennsylvania, which shows steel and cement manufacturing paired to suitable sinks as having the lowest levelized cost of capture, compression, and transportation.

Simplified models of rates of CO2 mineralization in Geologic Carbon Storage

Science.gov (United States)

DePaolo, D. J.; Zhang, S.

2017-12-01

Geologic carbon storage (GCS) reverses the flow of carbon to the atmosphere, returning the carbon to long-term geologic storage. Models suggest that most of the injected CO2 will be "trapped" in the subsurface by physical means, but the most risk-free and permanent form of carbon storage is as carbonate minerals (Ca,Mg,Fe)CO3. The transformation of CO2 to carbonate minerals requires supply of divalent cations by dissolution of silicate minerals. Available data suggest that rates of transformation are difficult to predict. We show that the chemical kinetic observations and experimental results, when reduced to a single timescale that describes the fractional rate at which cations are released to solution by mineral dissolution, show sufficiently systematic behavior that the rates of mineralization can be estimated with reasonable certainty. Rate of mineralization depends on both the abundance (determined by the reservoir rock mineralogy) and the rate at which cations are released by dissolution into pore fluid that has been acidified with dissolved CO2. Laboratory-measured rates and field observations give values spanning 8 to 10 orders of magnitude, but when evaluated in the context of reservoir-scale reactive transport simulations, this range becomes much smaller. Reservoir scale simulations indicate that silicate mineral dissolution and subsequent carbonate mineral precipitation occur at pH 4.5 to 6, fluid flow velocity less than 5m/yr, and 50-100 years or more after the start of injection. These constraints lead to estimates of 200 to 2000 years for conversion of 60-90% of injected CO2 when the reservoir rock has a sufficient volume fraction of divalent cation-bearing silicate minerals (ca. 20%), and confirms that when reservoir rock mineralogy is not favorable the fraction of CO2 converted to carbonate minerals is minimal over 104 years. A sufficient amount of reactive minerals represents the condition by which the available cations per volume of rock plus pore

Carbon Capture and Sequestration- A Review

Science.gov (United States)

Sood, Akash; Vyas, Savita

2017-08-01

The Drastic increase of CO2 emission in the last 30 years is due to the combustion of fossil fuels and it causes a major change in the environment such as global warming. In India, the emission of fossil fuels is developed in the recent years. The alternate energy sources are not sufficient to meet the values of this emission reduction and the framework of climate change demands the emission reduction, the CCS technology can be used as a mitigation tool which evaluates the feasibility for implementation of this technology in India. CCS is a process to capture the carbon dioxide from large sources like fossil fuel station to avoid the entrance of CO2 in the atmosphere. IPCC accredited this technology and its path for mitigation for the developing countries. In this paper, we present the technologies of CCS with its development and external factors. The main goal of this process is to avoid the release the CO2 into the atmosphere and also investigates the sequestration and mitigation technologies of carbon.

Developing low-cost carbon-based sorbents for Hg capture from flue gas

Energy Technology Data Exchange (ETDEWEB)

Ron Perry; Janos Lakatos; Colin E. Snape; Cheng-gong Sun [University of Nottingham (United Kingdom). UK Nottingham Fuel and Energy Centre, School of Chemical, Environmental and Mining Engineering

2005-07-01

To help reduce the cost of Hg capture, a number of low-cost carbons are being investigated, including tyre char, PFA carbons and gasification residues. This contribution reports the breakthrough capacities in fixed-bed screening tests for these materials in relation to those for commercial active carbons, including Norit FGD and the extent to which breakthrough capacities can be improved by MnO{sub 2} impregnation. 7 refs., 3 figs., 1 tab.

Range of engineering-geological properties for some carbonate rock complexes for Balkan peninsula

International Nuclear Information System (INIS)

Jovanovski, Milorad; Shpago, Azra; Peshevski, Igor

2010-01-01

The Carbonate Rock masses are a geological media with extremely complex states and properties, which has a certain influences on the mechanical and hydraulic behavior during construction and exploitation of engineering structures. Practical aspects of the problem analysis arise from the fact that the areas of Bosnia and Herzegovina, Macedonia and the entire Balkans is characterized by presence of wide areas covered with carbonate complexes, where large number of complex engineering structures have been, or shall be constructed in the future. In this context, their engineering-geological modeling is still a practical and scientific challenge. The analysis of engineering- geological properties is one of the main steps in forming of analytical and geotechnical models for complex rock structures. This article gives a data about the range for these properties, according to the results from an extensive investigation program. Some original correlations and testing results are given and they are compared with some published relations from the world. (Author)

Made-to-order metal-organic frameworks for trace carbon dioxide removal and air capture

KAUST Repository

Shekhah, Osama; Belmabkhout, Youssef; Chen, Zhijie; Guillerm, Vincent; Cairns, Amy; Adil, Karim; Eddaoudi, Mohamed

2014-01-01

Direct air capture is regarded as a plausible alternate approach that, if economically practical, can mitigate the increasing carbon dioxide emissions associated with two of the main carbon polluting sources, namely stationary power plants

Opportunities for early Carbon Capture, Utilisation and Storage development in China

Energy Technology Data Exchange (ETDEWEB)

Jansen, D. [ECN Biomass and Energy Efficiency, Petten (Netherlands)

2013-01-15

The outline of the presentation shows the following elements: China CCUS (Carbon Capture, Utilisation and Storage) policy, strategy and development status; International developments in CCUS; High-purity CO2 sources and potential EOR (Enhanced Oil Recovery) locations in China; Capture routes: (a) Separation technologies/processes, (b) CO2 purity specifications, compression and after treatment, (c) CO2 transportation options, (d) Associated Cost; Potential cost-effective full-chain CCUS projects in Shaanxi; Barriers to CCUS development in Shaanxi; and Conclusions.

Electrochemical Membrane for Carbon Dioxide Capture and Power Generation

Energy Technology Data Exchange (ETDEWEB)

Ghezel-Ayagh, Hossein [FuelCell Energy, Inc., Danbury, CT (United States)

2017-12-21

FuelCell Energy, Inc. (FCE), in collaboration with AECOM Corporation (formerly URS Corporation) and Pacific Northwest National Laboratory, has been developing a novel Combined Electric Power and Carbon-dioxide Separation (CEPACS) system. The CEPACS system is based on electrochemical membrane (ECM) technology derived from FCE’s carbonate fuel cell products featuring internal (methane steam) reforming and carrying the trade name of Direct FuelCell®. The unique chemistry of carbonate fuel cells offers an innovative approach for separation of CO₂ from existing fossil-fuel power plant exhaust streams (flue gases). The ECM-based CEPACS system has the potential to become a transformational CO₂-separation technology by working as two devices in one: it separates the CO₂ from the exhaust of other plants such as an existing coal-fired plant and simultaneously produces clean electric power at high efficiency using a supplementary fuel. The development effort was carried out under the U.S. Department of Energy (DOE) cooperative agreement DE-FE0007634. The overall objective of this project was to successfully demonstrate the ability of FCE’s ECM-based CEPACS system technology to separate ≥90% of the CO₂ from a simulated Pulverized Coal (PC) power plant flue gas stream and to compress the captured CO2 to a state that can be easily transported for sequestration or beneficial use. In addition, a key objective was to show, through the technical and economic feasibility study and bench scale testing, that the ECM-based CEPACS system is an economical alternative for CO₂ capture in PC power plants, and that it meets DOE’s objective related to the incremental cost of electricity (COE) for post-combustion CO₂ capture (no more than 35% increase in COE). The project was performed in three budget periods (BP). The specific objective for BP1 was to complete the Preliminary Technical and Economic Feasibility Study

Environmental issues and process risks for operation of carbon capture plant

Directory of Open Access Journals (Sweden)

Lajnert Radosław

2018-01-01

Full Text Available The scope of this publication is a presentation of environmental issues and process risks connected with operation an installation for carbon capture from waste gas. General technological assumptions, typical for demonstration plant for carbon capture from waste gas (DCCP with application of two different solutions – 30% water solution of monoethanoloamine (MEA and water solution with 30% AMP (2-amino-2-methyl-1-propanol and 10% piperazine have been described. The concept of DCCP installation was made for Łaziska Power Plant in Łaziska Górne owned by TAURON Wytwarzanie S.A. Main hazardous substances, typical for such installation, which can be dangerous for human life and health or for the environment have been presented. Pollution emission to the air, noise emission, waste water and solid waste management have been described. The environmental impact of the released substances has been stated. Reference to emission standards specified in regulations for considered substances has been done. Principles of risk analysis have been presented and main hazards in carbon dioxide absorption node and regeneration node have been evaluated.

Environmental issues and process risks for operation of carbon capture plant

Science.gov (United States)

Lajnert, Radosław; Nowak, Martyna; Telenga-Kopyczyńska, Jolanta

2018-01-01

The scope of this publication is a presentation of environmental issues and process risks connected with operation an installation for carbon capture from waste gas. General technological assumptions, typical for demonstration plant for carbon capture from waste gas (DCCP) with application of two different solutions - 30% water solution of monoethanoloamine (MEA) and water solution with 30% AMP (2-amino-2-methyl-1-propanol) and 10% piperazine have been described. The concept of DCCP installation was made for Łaziska Power Plant in Łaziska Górne owned by TAURON Wytwarzanie S.A. Main hazardous substances, typical for such installation, which can be dangerous for human life and health or for the environment have been presented. Pollution emission to the air, noise emission, waste water and solid waste management have been described. The environmental impact of the released substances has been stated. Reference to emission standards specified in regulations for considered substances has been done. Principles of risk analysis have been presented and main hazards in carbon dioxide absorption node and regeneration node have been evaluated.

The Oligocene carbonate platform of the Zagros Basin, SW Iran: An assessment of highly-complex geological heritage

Science.gov (United States)

Habibi, Tahereh; Ruban, Dmitry A.

2017-05-01

North Africa and the Middle East possess rich geological heritage, but the latter is yet to be fully identified and described. The Oligocene carbonate platform of the Zagros Basin in southwest Iran, which corresponds to the lower part of the Asmari Formation, has significant potential for geoconservation and geotourism. The types of the geological heritage, their value, and the possible geosites have been assessed. The studied deposits are interesting because of lithology (carbonate rocks), fossils (larger foraminifera, other microfossils, diverse marine invertebrates, fish microremains, and trace fossils), biostratigraphical developments, facies (homoclinal carbonate ramp) and signature of global events (glacioeustatic fluctuations), and outstanding hydrocarbon resources. The five main geological heritage types are sedimentary, palaeontological, stratigraphical, palaeogeographical, and economical, from which the palaeontological, palaeogeographical, and economical types are of global rank. The Khollar and Kavar sections in the Fars Province of Iran are recommended as geosites suitable for research, education, and tourism. The high complexity of the geological heritage linked to the Oligocene carbonate platform of the Zagros Basin implies the phenomenon of geodiversity should be understood with regard to the relationships between types and their values.

The geological carbon cycle and the global warming / climate debate

International Nuclear Information System (INIS)

Frank, F.

2013-01-01

The extensively cited seasonal carbon cycle describes the size and the annual fluxes between the temporary reservoirs (ocean, atmosphere, biosphere and soils). Compared with these large annual fluxes (approx. 200 GtC/y) the human contribution seems to be of minor amount and is currently (2011) in the range of 4-5%. However, in the geological carbon cycle, which describes the nearly equal amounts of input (volcanoes etc.) and output (sediments) into and from the temporary reservoirs, the human contribution has now reached 30-50 times the average natural level (9.5 Gt C/y versus ca. 0.2-0.3Gt C/y). In the long-term range (1-10x106y), the variable, but much smaller net imbalance between these geological sources und sinks was responsible for the atmospheric CO2-level in the last 400 My (since then comparable temporary reservoirs exist) and influenced via the various feedbacks the climate on earth. In nearly 95% of this long time the climate system was in (nearly) equilibrium conditions and changes occurred extremely slow. Whenever a certain range of higher rate of change of these driving forces were reached, it had - together with other effects - severe influence on the evolution of life, causing 5 large and many minor 'geological accidents'. Based on isotope geochemistry and a fairly good time resolution by orbitally tuned cyclostratigraphy (astrochronology) in the sedimentary record, we are able to quantify these rates of change with reasonable errors. It turns out that the present rate of change - caused by the C-based fossil energy use - is one to two orders of magnitude more rapid than these severe events (impacts excluded) in the earth system. A vast amount of data is available from the ice age cycles. Climate geology (e.g. the group of M. Sarnthein) made considerable progress in understanding the related geological/oceanic processes and proposed a reasonably constrained mass balance of CO2 during the last cycle, which could help us to understand the future

Canadian CO2 Capture and Storage Technology Network : promoting zero emissions technologies

International Nuclear Information System (INIS)

2004-11-01

This brochure provided information on some Canadian initiatives in carbon dioxide (CO 2 ) capture and storage. There has been growing interest in the implementation of components of CO 2 capture, storage and utilization technologies in Canada. Technology developments by the CANMET Energy Technology Centre concerning CO 2 capture using oxy-fuel combustion and amine separation were examined. Techniques concerning gasification of coal for electricity production and CO 2 capture were reviewed. Details of a study of acid gas underground injection were presented. A review of monitoring technologies in CO 2 storage in enhanced oil recovery was provided. Issues concerning the enhancement of methane recovery through the monitoring of CO 2 injected into deep coal beds were discussed. Storage capacity assessment of Canadian sedimentary basins, coal seams and oil and gas reservoirs were reviewed, in relation to their suitability for CO 2 sequestration. Details of the International Test Centre for Carbon Dioxide Capture in Regina, Saskatchewan were presented, as well as issues concerning the sequestration of CO 2 in oil sands tailings streams. A research project concerning the geologic sequestration of CO 2 and simultaneous CO 2 and methane production from natural gs hydrate reservoirs was also discussed. 12 figs.

Annual Report: Carbon Capture Simulation Initiative (CCSI) (30 September 2012)

Energy Technology Data Exchange (ETDEWEB)

Miller, David C. [National Energy Technology Lab. (NETL), Morgantown, WV (United States); Syamlal, Madhava [National Energy Technology Lab. (NETL), Morgantown, WV (United States); Cottrell, Roger [URS Corporation. (URS), San Francisco, CA (United States); National Energy Technology Lab. (NETL), Morgantown, WV (United States); Kress, Joel D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Sun, Xin [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sundaresan, S. [Princeton Univ., NJ (United States); Sahinidis, Nikolaos V. [Carnegie Mellon Univ., Pittsburgh, PA (United States); National Energy Technology Lab. (NETL), Morgantown, WV (United States); Zitney, Stephen E. [NETL; Bhattacharyya, D. [West Virginia Univ., Morgantown, WV (United States); National Energy Technology Lab. (NETL), Morgantown, WV (United States); Agarwal, Deb [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Tong, Charles [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Lin, Guang [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Dale, Crystal [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Engel, Dave [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Calafiura, Paolo [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Beattie, Keith [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Shinn, John [SynPatEco. Pleasant Hill, CA (United States)

2012-09-30

The Carbon Capture Simulation Initiative (CCSI) is a partnership among national laboratories, industry and academic institutions that is developing and deploying state-of-the-art computational modeling and simulation tools to accelerate the commercialization of carbon capture technologies from discovery to development, demonstration, and ultimately the widespread deployment to hundreds of power plants. The CCSI Toolset will provide end users in industry with a comprehensive, integrated suite of scientifically validated models, with uncertainty quantification (UQ), optimization, risk analysis and decision making capabilities. The CCSI Toolset incorporates commercial and open-source software currently in use by industry and is also developing new software tools as necessary to fill technology gaps identified during execution of the project. Ultimately, the CCSI Toolset will (1) enable promising concepts to be more quickly identified through rapid computational screening of devices and processes; (2) reduce the time to design and troubleshoot new devices and processes; (3) quantify the technical risk in taking technology from laboratory-scale to commercial-scale; and (4) stabilize deployment costs more quickly by replacing some of the physical operational tests with virtual power plant simulations. CCSI is organized into 8 technical elements that fall under two focus areas. The first focus area (Physicochemical Models and Data) addresses the steps necessary to model and simulate the various technologies and processes needed to bring a new Carbon Capture and Storage (CCS) technology into production. The second focus area (Analysis & Software) is developing the software infrastructure to integrate the various components and implement the tools that are needed to make quantifiable decisions regarding the viability of new CCS technologies. CCSI also has an Industry Advisory Board (IAB). By working closely with industry from the inception of the project to identify

U.S. Geological Survey Methodology Development for Ecological Carbon Assessment and Monitoring

Science.gov (United States)

Zhu, Zhi-Liang; Stackpoole, S.M.

2009-01-01

Ecological carbon sequestration refers to transfer and storage of atmospheric carbon in vegetation, soils, and aquatic environments to help offset the net increase from carbon emissions. Understanding capacities, associated opportunities, and risks of vegetated ecosystems to sequester carbon provides science information to support formulation of policies governing climate change mitigation, adaptation, and land-management strategies. Section 712 of the Energy Independence and Security Act (EISA) of 2007 mandates the Department of the Interior to develop a methodology and assess the capacity of our nation's ecosystems for ecological carbon sequestration and greenhouse gas (GHG) flux mitigation. The U.S. Geological Survey (USGS) LandCarbon Project is responding to the Department of Interior's request to develop a methodology that meets specific EISA requirements.

An architectural framework for developing intelligent applications for the carbon dioxide capture process

Energy Technology Data Exchange (ETDEWEB)

Luo, C.; Zhou, Q.; Chan, C.W. [Regina Univ., SK (Canada)

2009-07-01

This presentation reported on the development of automated application solutions for the carbon dioxide (CO{sub 2}) capture process. An architectural framework was presented for developing intelligent systems for the process system. The chemical absorption process consists of dozens of components. It therefore generates more than a hundred different types of data. Developing automated support for these tasks is desirable because the monitoring, analysis and diagnosis of the data is very complex. The proposed framework interacts with an implemented domain ontology for the CO{sub 2} capture process, which consists of information derived from senior operators of the CO{sub 2} pilot plant at the International Test Centre for Carbon Dioxide Capture at University of Regina. The well-defined library within the framework reduces development time and cost. The framework also has built-in web-based software components for data monitoring, management, and analysis. These components provide support for generating automated solutions for the CO{sub 2} capture process. An automated monitoring system that was also developed based on the architectural framework.

CQUESTRA, a risk and performance assessment code for geological sequestration of carbon dioxide

International Nuclear Information System (INIS)

LeNeveu, D.M.

2008-01-01

A computationally efficient semi-analytical code, CQUESTRA, has been developed for probabilistic risk assessment and rapid screening of potential sites for geological sequestration of carbon dioxide. The rate of dissolution and leakage from a trapped underground pool of carbon dioxide is determined. The trapped carbon dioxide could be mixed with hydrocarbons and other components to form a buoyant phase. The program considers potential mechanisms for escape from the geological formations such as the movement of the buoyant phase through failed seals in wellbores, the annulus around wellbores and through open fractures in the caprock. Plume animations of dissolved carbon dioxide in formation water around the wellbores are provided. Solubility, density and viscosity of the buoyant phase are determined by equations of state. Advection, dispersion, diffusion, buoyancy, aquifer flow rates and local formation fluid pressure are taken into account in the modeling of the carbon dioxide movement. Results from a hypothetical example simulation based on data from the Williston basin near Weyburn, Saskatchewan, indicate that this site is potentially a viable candidate for carbon dioxide sequestration. Sensitivity analysis of CQUESTRA indicates that criteria such as siting below aquifers with large flow rates and siting in reservoirs having fluid pressure below the pressure of the formations above can promote complete dissolution of the carbon dioxide during movement toward the surface, thereby preventing release to the biosphere. Formation of very small carbon dioxide bubbles within the fluid in the wellbores can also lead to complete dissolution

Development of environmental impact monitoring protocol for offshore carbon capture and storage (CCS): A biological perspective

International Nuclear Information System (INIS)

Kim, Hyewon; Kim, Yong Hoon; Kang, Seong-Gil; Park, Young-Gyu

2016-01-01

Offshore geologic storage of carbon dioxide (CO_2), known as offshore carbon capture and sequestration (CCS), has been under active investigation as a safe, effective mitigation option for reducing CO_2 levels from anthropogenic fossil fuel burning and climate change. Along with increasing trends in implementation plans and related logistics on offshore CCS, thorough risk assessment (i.e. environmental impact monitoring) needs to be conducted to evaluate potential risks, such as CO_2 gas leakage at injection sites. Gas leaks from offshore CCS may affect the physiology of marine organisms and disrupt certain ecosystem functions, thereby posing an environmental risk. Here, we synthesize current knowledge on environmental impact monitoring of offshore CCS with an emphasis on biological aspects and provide suggestions for better practice. Based on our critical review of preexisting literatures, this paper: 1) discusses key variables sensitive to or indicative of gas leakage by summarizing physico-chemical and ecological variables measured from previous monitoring cruises on offshore CCS; 2) lists ecosystem and organism responses to a similar environmental condition to CO_2 leakage and associated impacts, such as ocean acidification and hypercapnia, to predict how they serve as responsive indicators of short- and long-term gas exposure, and 3) discusses the designs of the artificial gas release experiments in fields and the best model simulation to produce realistic leakage scenarios in marine ecosystems. Based on our analysis, we suggest that proper incorporation of biological aspects will provide successful and robust long-term monitoring strategies with earlier detection of gas leakage, thus reducing the risks associated with offshore CCS. - Highlights: • This paper synthesizes the current knowledge on environmental impact monitoring of offshore Carbon Capture and Sequestration (CCS). • Impacts of CO_2 leakage (ocean acidification, hypercapnia) on marine

Development of environmental impact monitoring protocol for offshore carbon capture and storage (CCS): A biological perspective

Energy Technology Data Exchange (ETDEWEB)

Kim, Hyewon, E-mail: hyewon@ldeo.columbia.edu [Division of Biology and Paleo Environment, Lamont-Doherty Earth Observatory, Columbia University, Palisades, NY 10964 (United States); Kim, Yong Hoon, E-mail: Yong.Kim@rpsgroup.com [RPS ASA, 55 Village Square Drive, South Kingstown, RI 02879 (United States); Kang, Seong-Gil, E-mail: kangsg@kriso.re.kr [Offshore CCS Research Unit, Korea Research Institute of Ships and Ocean Engineering, 32 1312 Beon-gil, Yuseong-daero, Yuseong-gu, Deaejeon (Korea, Republic of); Park, Young-Gyu, E-mail: ypark@kiost.ac.kr [Ocean Circulation and Climate Change Research Center, Korea Institute of Ocean Science and Technology, 787 Haeanro, Ansan (Korea, Republic of)

2016-02-15

Offshore geologic storage of carbon dioxide (CO{sub 2}), known as offshore carbon capture and sequestration (CCS), has been under active investigation as a safe, effective mitigation option for reducing CO{sub 2} levels from anthropogenic fossil fuel burning and climate change. Along with increasing trends in implementation plans and related logistics on offshore CCS, thorough risk assessment (i.e. environmental impact monitoring) needs to be conducted to evaluate potential risks, such as CO{sub 2} gas leakage at injection sites. Gas leaks from offshore CCS may affect the physiology of marine organisms and disrupt certain ecosystem functions, thereby posing an environmental risk. Here, we synthesize current knowledge on environmental impact monitoring of offshore CCS with an emphasis on biological aspects and provide suggestions for better practice. Based on our critical review of preexisting literatures, this paper: 1) discusses key variables sensitive to or indicative of gas leakage by summarizing physico-chemical and ecological variables measured from previous monitoring cruises on offshore CCS; 2) lists ecosystem and organism responses to a similar environmental condition to CO{sub 2} leakage and associated impacts, such as ocean acidification and hypercapnia, to predict how they serve as responsive indicators of short- and long-term gas exposure, and 3) discusses the designs of the artificial gas release experiments in fields and the best model simulation to produce realistic leakage scenarios in marine ecosystems. Based on our analysis, we suggest that proper incorporation of biological aspects will provide successful and robust long-term monitoring strategies with earlier detection of gas leakage, thus reducing the risks associated with offshore CCS. - Highlights: • This paper synthesizes the current knowledge on environmental impact monitoring of offshore Carbon Capture and Sequestration (CCS). • Impacts of CO{sub 2} leakage (ocean acidification

Made-to-order metal-organic frameworks for trace carbon dioxide removal and air capture

KAUST Repository

Shekhah, Osama

2014-06-25

Direct air capture is regarded as a plausible alternate approach that, if economically practical, can mitigate the increasing carbon dioxide emissions associated with two of the main carbon polluting sources, namely stationary power plants and transportation. Here we show that metal-organic framework crystal chemistry permits the construction of an isostructural metal-organic framework (SIFSIX-3-Cu) based on pyrazine/copper(II) two-dimensional periodic 4 4 square grids pillared by silicon hexafluoride anions and thus allows further contraction of the pore system to 3.5 versus 3.84 for the parent zinc(II) derivative. This enhances the adsorption energetics and subsequently displays carbon dioxide uptake and selectivity at very low partial pressures relevant to air capture and trace carbon dioxide removal. The resultant SIFSIX-3-Cu exhibits uniformly distributed adsorption energetics and offers enhanced carbon dioxide physical adsorption properties, uptake and selectivity in highly diluted gas streams, a performance, to the best of our knowledge, unachievable with other classes of porous materials. 2014 Macmillan Publishers Limited.

Flexible dynamic operation of solar-integrated power plant with solvent based post-combustion carbon capture (PCC) process

International Nuclear Information System (INIS)

Qadir, Abdul; Sharma, Manish; Parvareh, Forough; Khalilpour, Rajab; Abbas, Ali

2015-01-01

Highlights: • Flexible operation of power and PCC plant may significantly increase operational revenue. • Higher optimal carbon capture rates observed with solar thermal energy input. • Solar thermal repowering of the power plant provides highest net revenue. • Constant optimal capture rate observed for one of the flexible operation cases. • Up to 42% higher revenue generation observed between two cases with solar input. - Abstract: This paper examines flexible operation of solvent-based post-combustion carbon capture (PCC) for the reduction of power plant carbon emissions while minimizing revenue loss due to the reduced power plant electricity output. The study is conducted using a model superstructure enveloping three plants; a power plant, a PCC plant and a solar thermal field where the power plant and PCC plant are operated flexibly under the influence of hourly electricity market and weather conditions. Reduced (surrogate) models for the reboiler duty and auxiliary power requirement for the carbon capture plant are generated and applied to simulate and compare four cases, (A) power plant with PCC, (B) power plant with solar assisted PCC, (C) power plant with PCC and solar repowering – variable net electricity output and (D) power plant with PCC and solar repowering – fixed net electricity output. Such analyses are conducted under dynamic conditions including power plant part-load operation while varying the capture rate to optimize the revenue of the power plant. Each case was simulated with a lower carbon price of $25/tonne-CO 2 and a higher price of $50/tonne-CO 2 . The comparison of cases B–D found that optimal revenue generation for case C can be up to 42% higher than that of solar-assisted PCC (case B). Case C is found to be the most profitable with the lowest carbon emissions intensity and is found to exhibit a constant capture rate for both carbon prices. The optimal revenue for case D is slightly lower than case C for the lower carbon

Technological, economic and financial prospects of carbon dioxide capture in the cement industry

International Nuclear Information System (INIS)

Li, Jia; Tharakan, Pradeep; Macdonald, Douglas; Liang, Xi

2013-01-01

Cement is the second largest anthropogenic emission source, contributing approximately 7% of global CO 2 emissions. Carbon dioxide capture and storage (CCS) technology is considered by the International Energy Agency (IEA) as an essential technology capable of reducing CO 2 emissions in the cement sector by 56% by 2050. The study compares CO 2 capture technologies for the cement manufacturing process and analyses the economic and financial issues in deploying CO 2 capture in the cement industry. Post-combustion capture with chemical absorption is regarded as a proven technology to capture CO 2 from the calcination process. Oxyfuel is less mature but Oxyfuel partial capture—which only recycles O 2 /CO 2 gas in the precalciner—is estimated to be more economic than post-combustion capture. Carbonate looping technologies are not yet commercial, but they have theoretical advantages in terms of energy consumption. In contrast with coal-fired power plants, CO 2 capture in the cement industry benefits from a higher concentration of CO 2 in the flue gas, but the benefit is offset by higher SO x and NO x levels and the smaller scale of emissions from each plant. Concerning the prospects for financing cement plant CO 2 capture, large cement manufacturers on average have a higher ROE (return on equity) and lower debt ratio, thus a higher discount rate should be considered for the cost analysis than in power plants. IEA estimates that the incremental cost for deploying CCS to decarbonise the global cement sector is in the range US$350–840 billion. The cost estimates for deploying state-of-the art post-combustion CO 2 capture technologies in cement plants are above $60 to avoid each tonne of CO 2 emissions. However, the expectation is that the current market can only provide a minority of financial support for CO 2 capture in cement plants. Public financial support and/or CO 2 utilisation will be essential to trigger large-scale CCS demonstration projects in the cement

Technical support for an enabling policy framework for carbon dioxide capture and geological storage. Task 3. Incentivising CO2 capture and storage in the EU

International Nuclear Information System (INIS)

De Coninck, H.; Groenenberg, H.

2007-03-01

To date CO2 capture and storage (CCS) is not deployed at a commercial scale, and a range of policy instruments could be used to provide adequate incentives for large scale deployment of CCS in the European Union. Five groups of incentives are discussed: (1) the EU Emissions Trading Scheme (weak and strong version); (2) Member-State-based public financial support through investment support, feed-in subsidies or a CO2 price guarantee; (3) an EU-level low-carbon portfolio standard with tradable certificates; (4) an EU-wide CCS obligation for all new fossil-fuel-based power capacity, and (5) public-private partnerships for realizing a CO2 pipeline infrastructure. The nature of the policy, mainly in case the scale of the instrument matters and much public financial is involved, determines whether it will be implemented by the EU or at the Member-State level. Support for CCS projects at the Member-State level, however, will require amendment of the Community Guidelines for State Aid for Environmental Protection

Impact of CO_2-enriched combustion air on micro-gas turbine performance for carbon capture

International Nuclear Information System (INIS)

Best, Thom; Finney, Karen N.; Ingham, Derek B.; Pourkashanian, Mohamed

2016-01-01

Power generation is one of the largest anthropogenic greenhouse gas emission sources; although it is now reducing in carbon intensity due to switching from coal to gas, this is only part of a bridging solution that will require the utilization of carbon capture technologies. Gas turbines, such as those at the UK Carbon Capture Storage Research Centre's Pilot-scale Advanced CO_2 Capture Technology (UKCCSRC PACT) National Core Facility, have high exhaust gas mass flow rates with relatively low CO_2 concentrations; therefore solvent-based post-combustion capture is energy intensive. Exhaust gas recirculation (EGR) can increase CO_2 levels, reducing the capture energy penalty. The aim of this paper is to simulate EGR through enrichment of the combustion air with CO_2 to assess changes to turbine performance and potential impacts on complete generation and capture systems. The oxidising air was enhanced with CO_2, up to 6.29%vol dry, impacting mechanical performance, reducing both engine speed by over 400 revolutions per minute and compression temperatures. Furthermore, it affected complete combustion, seen in changes to CO and unburned hydrocarbon emissions. This impacted on turbine efficiency, which increased specific fuel consumption (by 2.9%). CO_2 enhancement could therefore result in significant efficiency gains for the capture plant. - Highlights: • Experimental investigation of the impact of exhaust gas recirculation (EGR) on GT performance. • Combustion air was enhanced with CO_2 to simulate EGR. • EGR impact was ascertained by CO and unburned hydrocarbon changes. • Primary factor influencing performance was found to be oxidiser temperature. • Impact of CO_2 enhancement on post-combustion capture efficiency.

Pre-Combustion Carbon Dioxide Capture by a New Dual Phase Ceramic-Carbonate Membrane Reactor

Energy Technology Data Exchange (ETDEWEB)

Lin, Jerry Y. S. [Arizona State Univ., Tempe, AZ (United States)

2015-01-31

This report documents synthesis, characterization and carbon dioxide permeation and separation properties of a new group of ceramic-carbonate dual-phase membranes and results of a laboratory study on their application for water gas shift reaction with carbon dioxide separation. A series of ceramic-carbonate dual phase membranes with various oxygen ionic or mixed ionic and electronic conducting metal oxide materials in disk, tube, symmetric, and asymmetric geometric configurations was developed. These membranes, with the thickness of 10 μm to 1.5 mm, show CO₂ permeance in the range of 0.5-5×10^-7 mol·m^-2·s^-1·Pa^-1 in 500-900°C and measured CO₂/N₂ selectivity of up to 3000. CO₂ permeation mechanism and factors that affect CO₂ permeation through the dual-phase membranes have been identified. A reliable CO₂ permeation model was developed. A robust method was established for the optimization of the microstructures of ceramic-carbonate membranes. The ceramic-carbonate membranes exhibit high stability for high temperature CO₂ separations and water gas shift reaction. Water gas shift reaction in the dual-phase membrane reactors was studied by both modeling and experiments. It is found that high temperature syngas water gas shift reaction in tubular ceramic-carbonate dual phase membrane reactor is feasible even without catalyst. The membrane reactor exhibits good CO₂ permeation flux, high thermal and chemical stability and high thermal shock resistance. Reaction and separation conditions in the membrane reactor to produce hydrogen of 93% purity and CO₂ stream of >95% purity, with 90% CO₂ capture have been identified. Integration of the ceramic-carbonate dual-phase membrane reactor with IGCC process for carbon dioxide capture was analyzed. A methodology was developed to identify optimum operation conditions for a

Carbon dioxide capture and separation techniques for advanced power generation point sources

Energy Technology Data Exchange (ETDEWEB)

Pennline, H.W.; Luebke, D.R.; Morsi, B.I.; Heintz, Y.J.; Jones, K.L.; Ilconich, J.B.

2006-09-01

The capture/separation step for carbon dioxide (CO2) from large-point sources is a critical one with respect to the technical feasibility and cost of the overall carbon sequestration scenario. For large-point sources, such as those found in power generation, the carbon dioxide capture techniques being investigated by the in-house research area of the National Energy Technology Laboratory possess the potential for improved efficiency and costs as compared to more conventional technologies. The investigated techniques can have wide applications, but the research has focused on capture/separation of carbon dioxide from flue gas (postcombustion from fossil fuel-fired combustors) and from fuel gas (precombustion, such as integrated gasification combined cycle – IGCC). With respect to fuel gas applications, novel concepts are being developed in wet scrubbing with physical absorption; chemical absorption with solid sorbents; and separation by membranes. In one concept, a wet scrubbing technique is being investigated that uses a physical solvent process to remove CO2 from fuel gas of an IGCC system at elevated temperature and pressure. The need to define an ideal solvent has led to the study of the solubility and mass transfer properties of various solvents. Fabrication techniques and mechanistic studies for hybrid membranes separating CO2 from the fuel gas produced by coal gasification are also being performed. Membranes that consist of CO2-philic silanes incorporated into an alumina support or ionic liquids encapsulated into a polymeric substrate have been investigated for permeability and selectivity. An overview of two novel techniques is presented along with a research progress status of each technology.

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-01-01

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-07-15

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

Efficient capture of CO2 over ordered micro-mesoporous hybrid carbon nanosphere

Science.gov (United States)

Chen, Changwei; Yu, Yanke; He, Chi; Wang, Li; Huang, Huang; Albilali, Reem; Cheng, Jie; Hao, Zhengping

2018-05-01

Four kinds of carbon-based adsorbents (micro-mesoporous hybrid carbon nanosphere and N-doped hollow carbon sphere with single-, double- or ruga-shell morphology) with different structural and textural properties were prepared and systematically studied in CO2 capture. All synthesized samples possess high specific surface area (828-910 m2 g-1), large pore volume (0.71-1.81 cm3 g-1), and different micropore contents varied from 2.1% to 46.4%. Amongst, the ordered micro-mesoporous carbon nanosphere (OM-CNS) exhibits the best adsorption performance with CO2 uptake as high as 3.01 mmol g-1 under conditions of 298 K and 1.0 bar, better than most of the reported CO2 adsorbents. The excellent CO2 adsorption capacity of OM-CNS can be reasonably attributed to the synergistic effect of ordered mesopore channels and abundant structural micropores which are beneficial for the diffusion and trapping of CO2 adsorbate. Moreover, the OM-CNS shows excellent CO2 trapping selectivity and superior stability and recyclability, which endow the OM-CNS as a promising and environmental-friendly adsorbent for CO2 capture and separation under practical conditions.

Synthesis of polybenzoxazine based nitrogen-rich porous carbons for carbon dioxide capture

Science.gov (United States)

Wan, Liu; Wang, Jianlong; Feng, Chong; Sun, Yahui; Li, Kaixi

2015-04-01

Nitrogen-rich porous carbons (NPCs) were synthesized from 1,5-dihydroxynaphthalene, urea, and formaldehyde based on benzoxazine chemistry by a soft-templating method with KOH chemical activation. They possess high surface areas of 856.8-1257.8 m2 g-1, a large pore volume of 0.15-0.65 cm3 g-1, tunable pore structure, high nitrogen content (5.21-5.32 wt%), and high char yields. The amount of the soft-templating agent F127 has multiple influences on the textural and chemical properties of the carbons, affecting the surface area and pore structure, impacting the compositions of nitrogen species and resulting in an improvement of the CO2 capture performance. At 1 bar, high CO2 uptake of 4.02 and 6.35 mmol g-1 at 25 and 0 °C was achieved for the sample NPC-2 with a molar ratio of F127 : urea = 0.010 : 1. This can be attributed to its well-developed micropore structure and abundant pyridinic nitrogen, pyrrolic nitrogen and pyridonic nitrogen functionalities. The sample NPC-2 also exhibits a remarkable selectivity for CO2/N2 separation and a fast adsorption/desorption rate and can be easily regenerated. This suggests that the polybenzoxazine-based NPCs are desirable for CO2 capture because of possessing a high micropore surface area, a large micropore volume, appropriate pore size distribution, and a large number of basic nitrogen functionalities.Nitrogen-rich porous carbons (NPCs) were synthesized from 1,5-dihydroxynaphthalene, urea, and formaldehyde based on benzoxazine chemistry by a soft-templating method with KOH chemical activation. They possess high surface areas of 856.8-1257.8 m2 g-1, a large pore volume of 0.15-0.65 cm3 g-1, tunable pore structure, high nitrogen content (5.21-5.32 wt%), and high char yields. The amount of the soft-templating agent F127 has multiple influences on the textural and chemical properties of the carbons, affecting the surface area and pore structure, impacting the compositions of nitrogen species and resulting in an improvement of the

Ordered nanoporous carbon for increasing CO2 capture

International Nuclear Information System (INIS)

Yoo, Hye-Min; Lee, Seul-Yi; Park, Soo-Jin

2013-01-01

Ordered nanoporous carbons (ONCs) were prepared using a soft-templating method. The prepared ONCs materials were subjected to a controlled carbonization temperature over the temperature range, 700–1000 °C, to increase the specific surface area and total pore volume of ordered nanoporous carbon followed by carbonization of the phenolic resin. ONCs materials synthesized at various carbonization temperatures were used as adsorbents to improve the CO 2 adsorption efficiency. The surface properties of the ONCs materials were examined by X-ray photoelectron spectroscopy. The structural properties of the ONCs materials were analyzed by X-ray diffraction. The textural properties of the ONCs materials were examined using the N 2 /77 K adsorption isotherms according to the Brunauer–Emmett–Teller equation. The CO 2 adsorption capacity was measured by CO 2 isothermal adsorption at 298 K/30 bar and 298 K/1 bar. The carbonization temperature was found to have a major effect on the CO 2 adsorption capacity, resulting from the specific surface area and total pore volumes of the ONCs materials. - Graphical abstract: This schematic diagram described synthesis of ONCs. Highlights: ► ONCs materials can be prepared readily using the direct-triblock-copolymer-templating method. ► The distributions show that prominent development can be observed around the micro-pore region. ► The soft-templating method provides opportunities for controlling the pore structure of ONCs. ► From thermal power plants for CO2 capture by adsorption technology, is a new direction.

The economics of an efficient reliance on biomass, carbon capture and carbon sequestration in a Kyoto-style emissions control environment

International Nuclear Information System (INIS)

Yohe, G.W.; Carnegie Mellon University, Pittsburgh, PA

2001-01-01

This note employs the economics paradigm to sort through the complications of relying simultaneously on biomass fuels, carbon capture with active sequestration and passive carbon sequestration to meet Kyoto-style carbon emission limits. It does so by exploiting the structure of a tax cum repurchase scheme for carbon. Under such a scheme, the carbon content of fossil fuel should be taxed at the point of purchase at a price that matches the shadow price of the carbon emission limit, but carbon embedded in biomass fuel should go un-taxed. The price of biomass fuel would, though, have to reflect the marginal cost of any externalities it might cause and the opportunity cost of its land-use requirements. Captured carbon could be repurchased at a price equal to the shadow price of carbon, net of the cost of active sequestration, itself the sum of private and social marginal costs. Finally, the price of the passive sequestration of carbon should equal the shadow price of carbon, net of the opportunity cost of setting those resources aside. Since a marketable permit system would support direct estimates of the requisite shadow price of carbon, such a system would also provide direct information about base prices for the tax cum repurchase scheme. To support long-term investment in biomass supply and sequestration, though, changes over time in emission limits must be accomplished in a smooth and predictable manner. (author)

Valuing Metal-Organic Frameworks for Postcombustion Carbon Capture: A Benchmark Study for Evaluating Physical Adsorbents

KAUST Repository

Adil, Karim

2017-08-22

The development of practical solutions for the energy-efficient capture of carbon dioxide is of prime importance and continues to attract intensive research interest. Conceivably, the implementation of adsorption-based processes using different cycling modes, e.g., pressure-swing adsorption or temperature-swing adsorption, offers great prospects to address this challenge. Practically, the successful deployment of practical adsorption-based technologies depends on the development of made-to-order adsorbents expressing mutually two compulsory requisites: i) high selectivity/affinity for CO2 and ii) excellent chemical stability in the presence of impurities. This study presents a new comprehensive experimental protocol apposite for assessing the prospects of a given physical adsorbent for carbon capture under flue gas stream conditions. The protocol permits: i) the baseline performance of commercial adsorbents such as zeolite 13X, activated carbon versus liquid amine scrubbing to be ascertained, and ii) a standardized evaluation of the best reported metal-organic framework (MOF) materials for carbon dioxide capture from flue gas to be undertaken. This extensive study corroborates the exceptional CO2 capture performance of the recently isolated second-generation fluorinated MOF material, NbOFFIVE-1-Ni, concomitant with an impressive chemical stability and a low energy for regeneration. Essentially, the NbOFFIVE-1-Ni adsorbent presents the best compromise by satisfying all the required metrics for efficient CO2 scrubbing.

Predicting the performance uncertainty of a 1-MW pilot-scale carbon capture system after hierarchical laboratory-scale calibration and validation

Energy Technology Data Exchange (ETDEWEB)

Xu, Zhijie; Lai, Canhai; Marcy, Peter William; Dietiker, Jean-François; Li, Tingwen; Sarkar, Avik; Sun, Xin

2017-05-01

A challenging problem in designing pilot-scale carbon capture systems is to predict, with uncertainty, the adsorber performance and capture efficiency under various operating conditions where no direct experimental data exist. Motivated by this challenge, we previously proposed a hierarchical framework in which relevant parameters of physical models were sequentially calibrated from different laboratory-scale carbon capture unit (C2U) experiments. Specifically, three models of increasing complexity were identified based on the fundamental physical and chemical processes of the sorbent-based carbon capture technology. Results from the corresponding laboratory experiments were used to statistically calibrate the physical model parameters while quantifying some of their inherent uncertainty. The parameter distributions obtained from laboratory-scale C2U calibration runs are used in this study to facilitate prediction at a larger scale where no corresponding experimental results are available. In this paper, we first describe the multiphase reactive flow model for a sorbent-based 1-MW carbon capture system then analyze results from an ensemble of simulations with the upscaled model. The simulation results are used to quantify uncertainty regarding the design’s predicted efficiency in carbon capture. In particular, we determine the minimum gas flow rate necessary to achieve 90% capture efficiency with 95% confidence.

Carbon capture and storage: steering between necessity and realism

International Nuclear Information System (INIS)

Finon, D.; Damian, M.

2011-01-01

Carbon sequestration is the option that will make possible to keep fossil energies in the future energy mix. This technology could be used for fixed carbon emission sources like fossil power plants or oil refineries or steel works or cement factories. Today 3 technologies to capture carbon have to be considered: post-combustion, pre-combustion and oxy-combustion, these technologies are expected to be used equally. The second step is the construction of a network of gas pipelines to transport CO 2 to the storage place. The last step is the storage that can be done in ancient oil or natural gas fields or in deep coal layers on in deep salt aquifer. The latter being the most promising. With a carbon emission price comprised between 30 and 50 euros a tonne, carbon sequestration is expected to be economically competitive around 2030 under the condition that the feedback experience gained from the first industrial installations on a large scale have made investment costs drop sharply. Because of its need for important initial investment carbon sequestration appears to be as capitalistic as nuclear energy and will require public funding. Demonstration programs have been launched in Europe, United-States, Canada and Australia. (A.C.)

Carbon Dioxide Capture and Separation Techniques for Gasification-based Power Generation Point Sources

Energy Technology Data Exchange (ETDEWEB)

Pennline, H.W.; Luebke, D.R.; Jones, K.L.; Morsi, B.I. (Univ. of Pittsburgh, PA); Heintz, Y.J. (Univ. of Pittsburgh, PA); Ilconich, J.B. (Parsons)

2007-06-01

The capture/separation step for carbon dioxide (CO2) from large-point sources is a critical one with respect to the technical feasibility and cost of the overall carbon sequestration scenario. For large-point sources, such as those found in power generation, the carbon dioxide capture techniques being investigated by the in-house research area of the National Energy Technology Laboratory possess the potential for improved efficiency and reduced costs as compared to more conventional technologies. The investigated techniques can have wide applications, but the research has focused on capture/separation of carbon dioxide from flue gas (post-combustion from fossil fuel-fired combustors) and from fuel gas (precombustion, such as integrated gasification combined cycle or IGCC). With respect to fuel gas applications, novel concepts are being developed in wet scrubbing with physical absorption; chemical absorption with solid sorbents; and separation by membranes. In one concept, a wet scrubbing technique is being investigated that uses a physical solvent process to remove CO2 from fuel gas of an IGCC system at elevated temperature and pressure. The need to define an ideal solvent has led to the study of the solubility and mass transfer properties of various solvents. Pertaining to another separation technology, fabrication techniques and mechanistic studies for membranes separating CO2 from the fuel gas produced by coal gasification are also being performed. Membranes that consist of CO2-philic ionic liquids encapsulated into a polymeric substrate have been investigated for permeability and selectivity. Finally, dry, regenerable processes based on sorbents are additional techniques for CO2 capture from fuel gas. An overview of these novel techniques is presented along with a research progress status of technologies related to membranes and physical solvents.

Review of Quantitative Monitoring Methodologies for Emissions Verification and Accounting for Carbon Dioxide Capture and Storage for California’s Greenhouse Gas Cap-and-Trade and Low-Carbon Fuel Standard Programs

Energy Technology Data Exchange (ETDEWEB)

Oldenburg, Curtis M. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Earth Sciences Division; Birkholzer, Jens T. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Earth Sciences Division

2014-12-23

The Cap-and-Trade and Low Carbon Fuel Standard (LCFS) programs being administered by the California Air Resources Board (CARB) include Carbon Dioxide Capture and Storage (CCS) as a potential means to reduce greenhouse gas (GHG) emissions. However, there is currently no universal standard approach that quantifies GHG emissions reductions for CCS and that is suitable for the quantitative needs of the Cap-and-Trade and LCFS programs. CCS involves emissions related to the capture (e.g., arising from increased energy needed to separate carbon dioxide (CO₂) from a flue gas and compress it for transport), transport (e.g., by pipeline), and storage of CO₂ (e.g., due to leakage to the atmosphere from geologic CO₂ storage sites). In this project, we reviewed and compared monitoring, verification, and accounting (MVA) protocols for CCS from around the world by focusing on protocols specific to the geologic storage part of CCS. In addition to presenting the review of these protocols, we highlight in this report those storage-related MVA protocols that we believe are particularly appropriate for CCS in California. We find that none of the existing protocols is completely appropriate for California, but various elements of all of them could be adopted and/or augmented to develop a rigorous, defensible, and practical surface leakage MVA protocol for California. The key features of a suitable surface leakage MVA plan for California are that it: (1) informs and validates the leakage risk assessment, (2) specifies use of the most effective monitoring strategies while still being flexible enough to accommodate special or site-specific conditions, (3) quantifies stored CO₂, and (4) offers defensible estimates of uncertainty in monitored properties. California’s surface leakage MVA protocol needs to be applicable to the main CO₂ storage opportunities (in California and in other states with entities participating in California�

Hierarchically Porous Carbon Materials for CO ₂ Capture: The Role of Pore Structure

Energy Technology Data Exchange (ETDEWEB)

Estevez, Luis [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Barpaga, Dushyant [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Zheng, Jian [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Sabale, Sandip [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Patel, Rajankumar L. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Zhang, Ji-Guang [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; McGrail, B. Peter [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States; Motkuri, Radha Kishan [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States

2018-01-17

With advances in porous carbon synthesis techniques, hierarchically porous carbon (HPC) materials are being utilized as relatively new porous carbon sorbents for CO2 capture applications. These HPC materials were used as a platform to prepare samples with differing textural properties and morphologies to elucidate structure-property relationships. It was found that high microporous content, rather than overall surface area was of primary importance for predicting good CO2 capture performance. Two HPC materials were analyzed, each with near identical high surface area (~2700 m2/g) and colossally high pore volume (~10 cm3/g), but with different microporous content and pore size distributions, which led to dramatically different CO2 capture performance. Overall, large pore volumes obtained from distinct mesopores were found to significantly impact adsorption performance. From these results, an optimized HPC material was synthesized that achieved a high CO2 capacity of ~3.7 mmol/g at 25°C and 1 bar.

Environmental assessment of amine-based carbon capture Scenario modelling with life cycle assessment (LCA)

Energy Technology Data Exchange (ETDEWEB)

Brekke, Andreas; Askham, Cecilia; Modahl, Ingunn Saur; Vold, Bjoern Ivar; Johnsen, Fredrik Moltu

2012-07-01

This report contains a first attempt at introducing the environmental impacts associated with amines and derivatives in a life cycle assessment (LCA) of gas power production with carbon capture and comparing these with other environmental impacts associated with the production system. The report aims to identify data gaps and methodological challenges connected both to modelling toxicity of amines and derivatives and weighting of environmental impacts. A scenario based modelling exercise was performed on a theoretical gas power plant with carbon capture, where emission levels of nitrosamines were varied between zero (gas power without CCS) to a worst case level (outside the probable range of actual carbon capture facilities). Because of extensive research and development in the areas of solvents and emissions from carbon capture facilities in the latter years, data used in the exercise may be outdated and results should therefore not be taken at face value.The results from the exercise showed: According to UseTox, emissions of nitrosamines are less important than emissions of formaldehyde with regard to toxicity related to operation of (i.e. both inputs to and outputs from) a carbon capture facility. If characterisation factors for emissions of metals are included, these outweigh all other toxic emissions in the study. None of the most recent weighting methods in LCA include characterisation factors for nitrosamines, and these are therefore not part of the environmental ranking.These results shows that the EDecIDe project has an important role to play in developing LCA methodology useful for assessing the environmental performance of amine based carbon capture in particular and CCS in general. The EDecIDe project will examine the toxicity models used in LCA in more detail, specifically UseTox. The applicability of the LCA compartment models and site specificity issues for a Norwegian/Arctic situation will be explored. This applies to the environmental compartments

The national carbon capture center at the power systems development facility

Energy Technology Data Exchange (ETDEWEB)

None, None

2012-09-01

The Power Systems Development Facility (PSDF) is a state-of-the-art test center sponsored by the U.S. Department of Energy and dedicated to the advancement of clean coal technology. In addition to the development of advanced coal gasification processes, the PSDF features the National Carbon Capture Center (NCCC) to study CO2 capture from coal-derived syngas and flue gas. The NCCC includes multiple, adaptable test skids that allow technology development of CO2 capture concepts using coal-derived syngas and flue gas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity. During the Budget Period Three reporting period, efforts at the NCCC/PSDF focused on testing of pre-combustion CO2 capture and related processes; commissioning and initial testing at the post-combustion CO2 capture facilities; and operating the gasification process to develop gasification related technologies and for syngas generation to test syngas conditioning technologies.

THE NATIONAL CARBON CAPTURE CENTER AT THE POWER SYSTEMS DEVELOPMENT FACILITY

Energy Technology Data Exchange (ETDEWEB)

None, None

2011-05-11

The Power Systems Development Facility (PSDF) is a state-of-the-art test center sponsored by the U.S. Department of Energy and dedicated to the advancement of clean coal technology. In addition to the development of advanced coal gasification processes, the PSDF features the National Carbon Capture Center (NCCC) to study CO2 capture from coal-derived syngas and flue gas. The NCCC includes multiple, adaptable test skids that allow technology development of CO2 capture concepts using coal-derived syngas and flue gas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity. During the Budget Period Two reporting period, efforts at the PSDF/NCCC focused on new technology assessment and test planning; designing and constructing post-combustion CO2 capture facilities; testing of pre-combustion CO2 capture and related processes; and operating the gasification process to develop gasification related technologies and for syngas generation to test syngas conditioning technologies.

Alternative Layouts for the Carbon Capture with the Chilled Ammonia Process

DEFF Research Database (Denmark)

Valenti, Gianluca; Bonalumi, Davide; Fosbøl, Philip Loldrup

2013-01-01

Many alternatives are being investigated for the carbon capture, but none appears to have been proved as the choice for full-scale applications. This work considers the Chilled Ammonia Process for coal-fired Ultra Super Critical power plants. Three layouts are simulated with Aspen Plus and the Ex......Many alternatives are being investigated for the carbon capture, but none appears to have been proved as the choice for full-scale applications. This work considers the Chilled Ammonia Process for coal-fired Ultra Super Critical power plants. Three layouts are simulated with Aspen Plus...... substantially the electric loss due to stream extraction from the turbine. The simulations show that the net electric efficiency drops from 45.5% to 33.5-34.5%, the SPECCA index is 3.8-4.3 MJth kgCO2–1 and the heat duties are 2.7-2.9 MJth kgCO2–1. The performances may improve greatly upon optimization...

The National Carbon Capture Center at the Power Systems Development Facility

Energy Technology Data Exchange (ETDEWEB)

None, None

2014-12-30

The National Carbon Capture Center (NCCC) at the Power Systems Development Facility supports the Department of Energy (DOE) goal of promoting the United States’ energy security through reliable, clean, and affordable energy produced from coal. Work at the NCCC supports the development of new power technologies and the continued operation of conventional power plants under CO₂ emission constraints. The NCCC includes adaptable slipstreams that allow technology development of CO₂ capture concepts using coal-derived syngas and flue gas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity and accelerate their development path to commercialization. During its first contract period, from October 1, 2008, through December 30, 2014, the NCCC designed, constructed, and began operation of the Post-Combustion Carbon Capture Center (PC4). Testing of CO₂ capture technologies commenced in 2011, and through the end of the contract period, more than 25,000 hours of testing had been achieved, supporting a variety of technology developers. Technologies tested included advanced solvents, enzymes, membranes, sorbents, and associated systems. The NCCC continued operation of the existing gasification facilities, which have been in operation since 1996, to support the advancement of technologies for next-generation gasification processes and pre-combustion CO₂ capture. The gasification process operated for 13 test runs, supporting over 30,000 hours combined of both gasification and pre-combustion technology developer testing. Throughout the contract period, the NCCC incorporated numerous modifications to the facilities to accommodate technology developers and increase test capabilities. Preparations for further testing were ongoing to continue advancement of the most promising technologies for

The Potential Role of Natural Gas Power Plants with Carbon Capture and Storage as a Bridge to a Low-Carbon Future

Science.gov (United States)

Natural gas combined-cycle (NGCC) turbines with carbon capture and storage (CCS) are a promising technology for reducing carbon dioxide (CO2) emissions in the electric sector. However, the high cost and efficiency penalties associated with CCS, as well as methane leakage from nat...

76 FR 56982 - Announcement of Federal Underground Injection Control (UIC) Class VI Program for Carbon Dioxide (CO2

Science.gov (United States)

2011-09-15

...-9465-1] Announcement of Federal Underground Injection Control (UIC) Class VI Program for Carbon Dioxide... Injection Control (UIC) Class VI Program for Carbon Dioxide (CO 2 ) Geologic Sequestration (GS) Wells under... highlighted in the ``Report of the Interagency Task Force on Carbon Capture and Storage'' (August 2010), it is...

Environmental non-government organizations' perceptions of geologic sequestration

International Nuclear Information System (INIS)

Wong-Parodi, Gabrielle; Ray, Isha; Farrell, Alexander E

2008-01-01

Environmental non-governmental organizations (NGOs) have been influential in shaping public perceptions of environmental problems, their causes and potential solutions. Over the last decade, carbon capture and storage (CCS) has emerged as a potentially important technological response to climate change. In this paper we investigate how leading US NGOs perceive geologic sequestration, a potentially controversial part of CCS. We examine how and why their perceptions and strategies might differ, and if and how they plan to shape public perceptions of geologic sequestration. We approach these questions through semi-structured interviews with representatives from a range of NGOs, supplemented by content analysis of their documents. We find that while all the NGOs are committed to combating climate change, their views on CCS as a mitigation strategy vary considerably. We find that these views are correlated with NGOs' histories of activism and advocacy, as well as with their sources of funding. Overall, most of these NGOs accept the necessity of geologic sequestration, while only a small fraction do not

A Policy Strategy for Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2012-09-05

Successful deployment of carbon capture and storage (CCS) is critically dependent on comprehensive policy support. While policy plays an important role in the deployment of many low-carbon technologies, it is especially crucial for CCS. This is because, in contrast to renewable energy or applications of energy efficiency, CCS generates no revenue, nor other market benefits, so long as there is no price on CO2 emissions. It is both costly to install and, once in place, has increased operating costs. Effective, well-designed policy support is essential in overcoming these barriers and the subsequent deployment of CCS technology. This guide for policy makers aims to assist those involved in designing national and international policies around CCS. It covers development of CCS from its early stages through to wide-scale deployment of the technology. The focus is both on incentives for conventional fossil-fuel CCS and for bioenergy with CCS (BECCS).

Using improved technology for widespread application of a geological carbon sequestration study

Science.gov (United States)

Raney, J.

2013-12-01

The Kansas Geological Survey is part of an ongoing collaboration between DOE-NETL, academia, and the petroleum industry to investigate the feasibility of carbon utilization and storage in Kansas. Latest findings in the 25,000 mi2 study area in southern Kansas estimate CO2 storage capacity ranges from 8.8 to 75.5 billion metric tons in a deep Lower Orodovican-age Arbuckle saline aquifer. In addition, an estimated 100 million tonnes of CO2 could be used for extracting additional oil from Kansas' fields, making transitions to carbon management economic. This partnership has a rare opportunity to synchronize abundant, yet previously disseminated knowledge into a cohesive scientific process to optimize sequestration site selection and implementation strategies. Following a thorough characterization, a small-scale CO2 injection of 70,000 tonnes will be implemented in Wellington Field in Sumner County, including a five-plot miscible CO2-EOR flood of a Mississippian reservoir followed by the underlying Arbuckle saline aquifer. Best practices and lessons learned from the field study will improve estimates on CO2 storage capacity, plume migration models, and identify potential leakage pathways to pursue safe and effective geological carbon sequestration at commercial scales. A highly accessible and multifunctional online database is being developed throughout the study that integrates all acquired geological, physical, chemical, and hydrogeologic knowledge. This public database incorporates tens of thousands of data points into easily viewable formats for user downloads. An Interactive Project Map Viewer is a key mechanism to present the scientific research, and will delineate compartment candidates and reservoirs matching reference criteria or user defined attributes. This tool uses a familiar pan and zoom interface to filter regional project data or scale down to detailed digitized information from over 3,300 carefully selected preexisting Kansas wells. A Java-based log

Reduction of emissions and geological storage of CO2. Innovation an industrial stakes

International Nuclear Information System (INIS)

Mandil, C.; Podkanski, J.; Socolow, R.; Dron, D.; Reiner, D.; Horrocks, P.; Fernandez Ruiz, P.; Dechamps, P.; Stromberg, L.; Wright, I.; Gazeau, J.C.; Wiederkehr, P.; Morcheoine, A.; Vesseron, P.; Feron, P.; Feraud, A.; Torp, N.T.; Christensen, N.P.; Le Thiez, P.; Czernichowski, I.; Hartman, J.; Roulet, C.; Roberts, J.; Zakkour, P.; Von Goerne, G.; Armand, R.; Allinson, G.; Segalen, L.; Gires, J.M.; Metz, B.; Brillet, B.

2005-01-01

CO 2 emissions in the transport sector (cars and aviation) by A. Morcheoine (ADEME), The contribution of biofuels and alternative fuels to reducing CO 2 emissions in the transport sector by I. Drescher (Volkswagen AG). Session III - Technological progress in the capture and geological storage of CO 2 : European projects on CO 2 capture and storage by P. Dechamps (European Commission, Research Energy Conversion and Transport); Capture of CO 2 : Innovative CO 2 capture concepts by P. Feron (TNO), Capture of CO 2 in pre- and oxy-combustion by A. Feraud, N. Otter (Alstom); Geological storage of CO 2 : Geological storage capacity by N.P. Christensen (GEUS), Feedback from industrial CO 2 storage projects by T. Torp (Statoil), The main avenues of current research by P. Le Thiez (IFP) and I. Czernichowski (BRGM), Long-term industrial experience with underground gas storage by J. Hartman (GDF). Session IV - Regulatory, economic and financial aspects. Legal and regulatory framework for capture and geological storage: UK's perspective on the regulatory framework for CO 2 storage by J. Roberts (DEFRA-UK), Monitoring and reporting of CCS in the European Union Emission Trading Scheme by P. Zakkour (ERM), Social need and public questions and perceptions by G. von Goerne (Greenpeace); Economic and financial impact: The costs of CCS by G. Allinson (CO 2 -CRC), The characteristics of CO 2 markets: players, volumes exchanged, and term and spot transaction prices by L. Segalen (European Carbon Fund), CO 2 management by J.M. Gires (Total), The forthcoming IPCC special report on carbon dioxide capture and storage by B. Metz (IPCC Working Group III). Closing Address by Bernard Brillet, Ministry for Higher Education and Research. (J.S.)

Modification of activated carbon using nitration followed by reduction for carbon dioxide capture

Energy Technology Data Exchange (ETDEWEB)

Shafeeyan, Mohammad Saleh; Houshmand, Amirhossein; Arami-Niya, Arash; Daud, Wan Mohd AshiWan [Dept. of Chemical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur (Malaysia); Razaghizadeh, Hosain [Dept. of Faculty of Environment and Energy, Research and Science Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of)

2015-02-15

Activated carbon (AC) samples were modified using nitration followed by reduction to enhance their CO{sub 2} adsorption capacities. Besides characterization of the samples, investigation of CO{sub 2} capture performance was conducted by CO{sub 2} isothermal adsorption, temperature-programmed (TP) CO{sub 2} adsorption, cyclic CO{sub 2} adsorption–desorption, and dynamic CO{sub 2} adsorption tests. Almost all modified samples showed a rise in the amount of CO{sub 2} adsorbed when the comparison is made in unit surface area. On the other hand, some of the samples displayed a capacity superior to that of the parent material when compared in mass unit, especially at elevated temperatures. Despite ⁓65% decrease in the surface area, TP-CO{sub 2} adsorption of the best samples exhibited increases of ⁓10 and 70% in CO{sub 2} capture capacity at 30 and 100 °C, respectively.

Geologic framework for the national assessment of carbon dioxide storage resources—Southern Rocky Mountain Basins: Chapter M in Geologic framework for the national assessment of carbon dioxide storage resources

Science.gov (United States)

Merrill, Matthew D.; Drake, Ronald M.; Buursink, Marc L.; Craddock, William H.; East, Joseph A.; Slucher, Ernie R.; Warwick, Peter D.; Brennan, Sean T.; Blondes, Madalyn S.; Freeman, Philip A.; Cahan, Steven M.; DeVera, Christina A.; Lohr, Celeste D.; Warwick, Peter D.; Corum, Margo D.

2016-06-02

The U.S. Geological Survey has completed an assessment of the potential geologic carbon dioxide storage resources in the onshore areas of the United States. To provide geological context and input data sources for the resources numbers, framework documents are being prepared for all areas that were investigated as part of the national assessment. This report, chapter M, is the geologic framework document for the Uinta and Piceance, San Juan, Paradox, Raton, Eastern Great, and Black Mesa Basins, and subbasins therein of Arizona, Colorado, Idaho, Nevada, New Mexico, and Utah. In addition to a summary of the geology and petroleum resources of studied basins, the individual storage assessment units (SAUs) within the basins are described and explanations for their selection are presented. Although appendixes in the national assessment publications include the input values used to calculate the available storage resource, this framework document provides only the context and source of the input values selected by the assessment geologists. Spatial-data files of the boundaries for the SAUs, and the well-penetration density of known well bores that penetrate the SAU seal, are available for download with the release of this report.

Real-time monitoring of emissions from monoethanolamine-based industrial scale carbon capture facilities.

Science.gov (United States)

Zhu, Liang; Schade, Gunnar Wolfgang; Nielsen, Claus Jørgen

2013-12-17

We demonstrate the capabilities and properties of using Proton Transfer Reaction time-of-flight mass spectrometry (PTR-ToF-MS) to real-time monitor gaseous emissions from industrial scale amine-based carbon capture processes. The benchmark monoethanolamine (MEA) was used as an example of amines needing to be monitored from carbon capture facilities, and to describe how the measurements may be influenced by potentially interfering species in CO2 absorber stack discharges. On the basis of known or expected emission compositions, we investigated the PTR-ToF-MS MEA response as a function of sample flow humidity, ammonia, and CO2 abundances, and show that all can exhibit interferences, thus making accurate amine measurements difficult. This warrants a proper sample pretreatment, and we show an example using a dilution with bottled zero air of 1:20 to 1:10 to monitor stack gas concentrations at the CO2 Technology Center Mongstad (TCM), Norway. Observed emissions included many expected chemical species, dominantly ammonia and acetaldehyde, but also two new species previously not reported but emitted in significant quantities. With respect to concerns regarding amine emissions, we show that accurate amine quantifications in the presence of water vapor, ammonia, and CO2 become feasible after proper sample dilution, thus making PTR-ToF-MS a viable technique to monitor future carbon capture facility emissions, without conventional laborious sample pretreatment.

Polymer-encapsulated carbon capture liquids that tolerate precipitation of solids for increased capacity

Energy Technology Data Exchange (ETDEWEB)

Aines, Roger D; Bourcier, William L; Spadaccini, Christopher M; Stolaroff, Joshuah K

2015-02-03

A system for carbon dioxide capture from flue gas and other industrial gas sources utilizes microcapsules with very thin polymer shells. The contents of the microcapsules can be liquids or mixtures of liquids and solids. The microcapsules are exposed to the flue gas and other industrial gas and take up carbon dioxide from the flue gas and other industrial gas and eventual precipitate solids in the capsule.

Wellbore cement fracture evolution at the cement–basalt caprock interface during geologic carbon sequestration

Energy Technology Data Exchange (ETDEWEB)

Jung, Hun Bok; Kabilan, Senthil; Carson, James P.; Kuprat, Andrew P.; Um, Wooyong; Martin, Paul F.; Dahl, Michael E.; Kafentzis, Tyler A.; Varga, Tamas; Stephens, Sean A.; Arey, Bruce W.; Carroll, KC; Bonneville, Alain; Fernandez, Carlos A.

2014-08-07

Composite Portland cement-basalt caprock cores with fractures, as well as neat Portland cement columns, were prepared to understand the geochemical and geomechanical effects on the integrity of wellbores with defects during geologic carbon sequestration. The samples were reacted with CO2-saturated groundwater at 50 ºC and 10 MPa for 3 months under static conditions, while one cement-basalt core was subjected to mechanical stress at 2.7 MPa before the CO2 reaction. Micro-XRD and SEM-EDS data collected along the cement-basalt interface after 3-month reaction with CO2-saturated groundwater indicate that carbonation of cement matrix was extensive with the precipitation of calcite, aragonite, and vaterite, whereas the alteration of basalt caprock was minor. X-ray microtomography (XMT) provided three-dimensional (3-D) visualization of the opening and interconnection of cement fractures due to mechanical stress. Computational fluid dynamics (CFD) modeling further revealed that this stress led to the increase in fluid flow and hence permeability. After the CO2-reaction, XMT images displayed that calcium carbonate precipitation occurred extensively within the fractures in the cement matrix, but only partially along the fracture located at the cement-basalt interface. The 3-D visualization and CFD modeling also showed that the precipitation of calcium carbonate within the cement fractures after the CO2-reaction resulted in the disconnection of cement fractures and permeability decrease. The permeability calculated based on CFD modeling was in agreement with the experimentally determined permeability. This study demonstrates that XMT imaging coupled with CFD modeling represent a powerful tool to visualize and quantify fracture evolution and permeability change in geologic materials and to predict their behavior during geologic carbon sequestration or hydraulic fracturing for shale gas production and enhanced geothermal systems.

Preliminary carbon dioxide capture technical and economic feasibility study evaluation of carbon dioxide capture from existing fired plants by hybrid sorption using solid sorbents

Energy Technology Data Exchange (ETDEWEB)

Benson, Steven; Envergex, Srivats; Browers, Bruce; Thumbi, Charles

2013-01-01

Barr Engineering Co. was retained by the Institute for Energy Studies (IES) at University of North Dakota (UND) to conduct a technical and economic feasibility analysis of an innovative hybrid sorbent technology (CACHYS™) for carbon dioxide (CO2) capture and separation from coal combustion–derived flue gas. The project team for this effort consists of the University of North Dakota, Envergex LLC, Barr Engineering Co., and Solex Thermal Science, along with industrial support from Allete, BNI Coal, SaskPower, and the North Dakota Lignite Energy Council. An initial economic and feasibility study of the CACHYS™ concept, including definition of the process, development of process flow diagrams (PFDs), material and energy balances, equipment selection, sizing and costing, and estimation of overall capital and operating costs, is performed by Barr with information provided by UND and Envergex. The technology—Capture from Existing Coal-Fired Plants by Hybrid Sorption Using Solid Sorbents Capture (CACHYS™)—is a novel solid sorbent technology based on the following ideas: reduction of energy for sorbent regeneration, utilization of novel process chemistry, contactor conditions that minimize sorbent-CO2 heat of reaction and promote fast CO2 capture, and a low-cost method of heat management. The technology’s other key component is the use of a low-cost sorbent.

Kinetic study of a Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

DEFF Research Database (Denmark)

Bonalumi, Davide; Lillia, Stefano; Valenti, Gianluca

2017-01-01

This paper focuses on carbon capture in an Ultra Super Critical power plant. The technology selected for CO2 capture is based on cooled ammonia scrubbing in post-combustion mode, as recently investigated by the authors in another work. Here, a rate-based approach is adopted. In detail, a specific...

Climate Strategy with CO2 Capture from the Air

Energy Technology Data Exchange (ETDEWEB)

Keith, D.W. [Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive NW, Calgary, AB (Canada); Ha-Duong, M. [CNRS-CIRED, Campus du Jardin Tropical, 45 bis, av. de la Belle Gabrielle, 94736 Nogent sur Marne CEDEX (France); Stolaroff, J.K. [Department of Engineering and Public Policy, Carnegie Mellon University, 5000 Forbes Ave, Pittsburgh, PA 15213 (United States)

2006-01-15

It is physically possible to capture CO2 directly from the air and immobilize it in geological structures. Air capture differs from conventional mitigation in three key aspects. First, it removes emissions from any part of the economy with equal ease or difficulty, so its cost provides an absolute cap on the cost of mitigation. Second, it permits reduction in concentrations faster than the natural carbon cycle: the effects of irreversibility are thus partly alleviated. Third, because it is weakly coupled to existing energy infrastructure, air capture may offer stronger economies of scale and smaller adjustment costs than the more conventional mitigation technologies. We assess the ultimate physical limits on the amount of energy and land required for air capture and describe two systems that might achieve air capture at prices under 200 and 500 $/tC using current technology. Like geoengineering, air capture limits the cost of a worst-case climate scenario. In an optimal sequential decision framework with uncertainty, existence of air capture decreases the need for near-term precautionary abatement. The long-term effect is the opposite; assuming that marginal costs of mitigation decrease with time while marginal climate change damages increase, then air capture increases long-run abatement. Air capture produces an environmental Kuznets curve, in which concentrations are returned to preindustrial levels.

Canada's carbon capture and storage initiatives

Energy Technology Data Exchange (ETDEWEB)

Malone, Alexandra; Mitrovic, Milenka; Grant, Andrea

2010-09-15

Carbon capture and storage (CCS) is a critical technology for Canada to make meaningful emissions reductions in the fossil fuels sector. Canada is a global leader in CCS, and both federal and provincial governments are taking action to advance the deployment of this technology, including allocating over CAD 3.5 billion in public funding to CCS. These investments support several interdependent initiatives focusing on addressing the challenges facing CCS, supporting innovation, accelerating deployment, and facilitating information sharing. Canada is also committed to working internationally to ensure that our efforts at home contribute to the overall global advancement of CCS.

Prospects for carbon capture and sequestration technologies assuming their technological learning

International Nuclear Information System (INIS)

Riahi, Keywan; Rubin, Edward S.; Schrattenholzer, Leo

2004-01-01

This paper analyzes potentials of carbon capture and sequestration technologies (CCS) in a set of long-term energy-economic-environmental scenarios based on alternative assumptions for technological progress of CCS. In order to get a reasonable guide to future technological progress in managing CO 2 emissions, we review past experience in controlling sulfur dioxide emissions (SO 2 ) from power plants. By doing so, we quantify a 'learning curve' for CCS, which describes the relationship between the improvement of costs due to accumulation of experience in CCS construction. We incorporate the learning curve into the energy modeling framework MESSAGE-MACRO and develop greenhouse gas emissions scenarios of economic, demographic, and energy demand development, where alternative policy cases lead to the stabilization of atmospheric CO 2 concentrations at 550 parts per million by volume (ppmv) by the end of the 21st century. Due to the assumed technological learning, costs of the emissions reduction for CCS drop rapidly and in parallel with the massive introduction of CCS on the global scale. Compared to scenarios based on static cost assumptions for CCS, the contribution of carbon sequestration is about 50 percent higher in the case of learning resulting in cumulative sequestration of CO 2 ranging from 150 to 250 billion (10 9 ) tons carbon during the 21st century. The results illustrate that carbon capture and sequestration is one of the obvious priority candidates for long-term technology policies and enhanced R and D efforts to hedge against the risk associated with high environmental impacts of climate change

Carbon Capture and Storage Development Trends from a Techno-Paradigm Perspective

Directory of Open Access Journals (Sweden)

Bobo Zheng

2014-08-01

Full Text Available The world’s energy needs have been continually growing over the past decade, yet fossil fuels are limited. Renewable energies are becoming more prevalent, but are still a long way from being commonplace worldwide. Literature mining is applied to review carbon capture and storage (CCS development trends and to develop and examine a novel carbon capture and storage technological paradigm (CCSTP, which incorporates CCSTP competition, diffusion and shift. This paper first provides an overview of the research and progress in CCS technological development, then applies a techno-paradigm theory to analyze CCSTP development and to provide a guide for future CCS technological trends. CCS could avoid CO2 being released into the atmosphere. Moreover, bioenergy with CCS (BECCS can make a significant contribution to a net removal of anthropogenic CO2 emissions. In this study, we compare the different CCSTP developmental paths and the conventional techno-paradigm by examining the S-curves. The analyses in this paper provide a useful guide for scholars seeking new inspiration in their research and for potential investors who are seeking to invest research funds in more mature technologies. We conclude that political barriers and public acceptance are the major distinctions between the CCSTP and the conventional techno-paradigm. It is expected that policy instruments and economic instruments are going to play a pivotal role in the accomplishment of global carbon reduction scenarios.

Sponges with covalently tethered amines for high-efficiency carbon capture

KAUST Repository

Qi, Genggeng

2014-12-12

© 2014 Macmillan Publishers Limited. All rights reserved. Adsorption using solid amine sorbents is an attractive emerging technology for energy-efficient carbon capture. Current syntheses for solid amine sorbents mainly based on physical impregnation or grafting-to methods (for example, aminosilane-grafting) lead to limited sorbent performance in terms of stability and working capacity, respectively. Here we report a family of solid amine sorbents using a grafting-from synthesis approach and synthesized by cationic polymerization of oxazolines on mesoporous silica. The sorbent with high amount of covalently tethered amines shows fast adsorption rate, high amine efficiency and sorbent capacity well exceeding the highest value reported to date for lowerature carbon dioxide sorbents under simulated flue gas conditions. The demonstrated efficiency of the new amine-immobilization chemistry may open up new avenues in the development of advanced carbon dioxide sorbents, as well as other nitrogen-functionalized systems.

The performance of the Norwegian carbon dioxide, capture and storage innovation system

NARCIS (Netherlands)

Alphen, K. van; Ruijven, Jochem van; Kasa, Sjur; Hekkert, M.P.; Turkenburg, W.C.

2009-01-01

In order to take up Norway's twin challenge of reducing CO2 emissions, while meeting its growing energy demand with domestic resources, the deployment of carbon capture and storage (CCS) plays an important role in Norwegian energy policies. This study uses the Functions of Innovation Systems

Assessment of the role of micropore size and N-doping in CO2 capture by porous carbons.

Science.gov (United States)

Sevilla, Marta; Parra, Jose B; Fuertes, Antonio B

2013-07-10

The role of micropore size and N-doping in CO2 capture by microporous carbons has been investigated by analyzing the CO2 adsorption properties of two types of activated carbons with analogous textural properties: (a) N-free carbon microspheres and (b) N-doped carbon microspheres. Both materials exhibit a porosity made up exclusively of micropores ranging in size between micropores with a size below 0.8 nm. It was also observed that the CO2 capture capacities of undoped and N-doped carbons are analogous which shows that the nitrogen functionalities present in these N-doped samples do not influence CO2 adsorption. Taking into account the temperature invariance of the characteristic curve postulated by the Dubinin theory, we show that CO2 uptakes can be accurately predicted by using the adsorption data measured at just one temperature.

Clean coal technologies. The capture and geological storage of CO2 - Panorama 2008

International Nuclear Information System (INIS)

2008-01-01

There is no longer any doubt about the connection between carbon dioxide emissions of human origin and global warming. Nearly 40% of world CO 2 emissions are generated by the electricity production sector, in which the combustion of coal - developing at a roaring pace, especially in China - accounts for a good proportion of the total. At a time when the reduction of greenhouse gases has become an international priority, this growth is a problem. Unless CO 2 capture and storage technologies are implemented, it will be very difficult to contain global warming

Developing low-cost carbon-based sorbents for Hg capture from flue gas

Energy Technology Data Exchange (ETDEWEB)

Perry, R.; Lakatos, J.; Snape, C.E.; Sun, C. [University of Nottingham, Nottingham (United Kingdom). Nottingham Fuel and Energy Centre

2005-07-01

To help reduce the cost of Hg capture from flue gas a number of low-cost carbons are being investigated, including activated tyre char and PFA carbon, in conjunction with some of the pre-treatments that have been found to be effective for commercial actived carbons. Experimental conditions for screening the sorbents have been selected to determine breakthrough capacities rapidly. The unactivated carbons have low breakthrough capacities under the test conditions employed (around 0.1 mg g{sup -1}) but these improve upon steam activation (around 0.25 mg g{sup -1}) but are still lower than those of non-impregnated commercial activated carbons (around 0.4-0.7 mg g{sup -1}), due to their lower surface areas. Comparable improvements to the commercial carbons have been achieved for impregnation treatments, including sulfur and bromine. However, certain gasification chars do have much higher breakthrough capacities than commercial carbons used for flue gas injection. Manganese oxide impregnation with low concentration is particularly effective for the activated and unactivated carbons giving breakthrough capacities comparable to the commercial carbons. Pointers for further increasing breakthrough and equilibrium capacities for carbon-based sorbents are discussed. 7 refs., 1 fig., 3 tabs.

Selection of microalgae and cyanobacteria strains for bicarbonate-based integrated carbon capture and algae production system.

Science.gov (United States)

Chi, Zhanyou; Elloy, Farah; Xie, Yuxiao; Hu, Yucai; Chen, Shulin

2014-01-01

Using microalgae to capture CO2 from flue gas is an ideal way to reduce CO2 emission, but this is challenged by the high cost of carbon capture and transportation. To address this problem, a bicarbonate-based integrated carbon capture and algae production system (BICCAPS) has been proposed, in which bicarbonate is used for algae culture, and the regenerated carbonate from this process can be used to capture more CO2. High-concentration bicarbonate is obligate for the BICCAPS. Thus, different strains of microalgae and cyanobacteria were tested in this study for their capability to grow in high-concentration NaHCO3. The highest NaHCO3 concentrations they are tolerant to were determined as 0.30 M for Synechocystis sp. PCC6803, 0.60 M for Cyanothece sp., 0.10 M for Chlorella sorokiniana, 0.60 M for Dunaliella salina, and 0.30 M for Dunaliella viridis and Dunaliella primolecta. In further study, biomass production from culture of D. primolecta in an Erlenmeyer flask with either 0.30 M NaHCO3 or 2 % CO2 bubbling was compared, and no significant difference was detected. This indicates BICCAPS can reach the same biomass productivity as regular CO2 bubbling culture, and it is promising for future application.

Carbon dioxide capture processes: Simulation, design and sensitivity analysis

DEFF Research Database (Denmark)

Zaman, Muhammad; Lee, Jay Hyung; Gani, Rafiqul

2012-01-01

equilibrium and associated property models are used. Simulations are performed to investigate the sensitivity of the process variables to change in the design variables including process inputs and disturbances in the property model parameters. Results of the sensitivity analysis on the steady state...... performance of the process to the L/G ratio to the absorber, CO2 lean solvent loadings, and striper pressure are presented in this paper. Based on the sensitivity analysis process optimization problems have been defined and solved and, a preliminary control structure selection has been made.......Carbon dioxide is the main greenhouse gas and its major source is combustion of fossil fuels for power generation. The objective of this study is to carry out the steady-state sensitivity analysis for chemical absorption of carbon dioxide capture from flue gas using monoethanolamine solvent. First...

System-level modeling for economic evaluation of geological CO2 storage in gas reservoirs

International Nuclear Information System (INIS)

Zhang, Yingqi; Oldenburg, Curtis M.; Finsterle, Stefan; Bodvarsson, Gudmundur S.

2007-01-01

One way to reduce the effects of anthropogenic greenhouse gases on climate is to inject carbon dioxide (CO 2 ) from industrial sources into deep geological formations such as brine aquifers or depleted oil or gas reservoirs. Research is being conducted to improve understanding of factors affecting particular aspects of geological CO 2 storage (such as storage performance, storage capacity, and health, safety and environmental (HSE) issues) as well as to lower the cost of CO 2 capture and related processes. However, there has been less emphasis to date on system-level analyses of geological CO 2 storage that consider geological, economic, and environmental issues by linking detailed process models to representations of engineering components and associated economic models. The objective of this study is to develop a system-level model for geological CO 2 storage, including CO 2 capture and separation, compression, pipeline transportation to the storage site, and CO 2 injection. Within our system model we are incorporating detailed reservoir simulations of CO 2 injection into a gas reservoir and related enhanced production of methane. Potential leakage and associated environmental impacts are also considered. The platform for the system-level model is GoldSim [GoldSim User's Guide. GoldSim Technology Group; 2006, http://www.goldsim.com]. The application of the system model focuses on evaluating the feasibility of carbon sequestration with enhanced gas recovery (CSEGR) in the Rio Vista region of California. The reservoir simulations are performed using a special module of the TOUGH2 simulator, EOS7C, for multicomponent gas mixtures of methane and CO 2 . Using a system-level modeling approach, the economic benefits of enhanced gas recovery can be directly weighed against the costs and benefits of CO 2 injection

Mining-related environmental impacts of carbon mitigation; Coal-based carbon capture and sequestration and wind-enabling transmission expansion

Energy Technology Data Exchange (ETDEWEB)

Grubert, Emily

2010-09-15

Carbon mitigation can occur by preventing generation of greenhouse gases or by preventing emissions from entering the atmosphere. Accordingly, increasing the use of wind energy or carbon capture and storage (CCS) at coal-fired power plants could reduce carbon emissions. This work compares the direct mining impacts of increased coal demand associated with CCS with those of increased aluminum demand for expanding transmission systems to enable wind power incorporation. Aluminum needs for expanded transmission probably represent a one-time need for about 1.5% of Jamaica's annual bauxite production, while CCS coal needs for the same mitigation could almost double US coal demand.

Coal reserves and resources as well as potentials for underground coal gasification in connection with carbon capture and storage (CCS)

Science.gov (United States)

Ilse, Jürgen

2010-05-01

. However, these otherwise unprofitable coal deposits can be mined economically by means of underground coal gasification, during which coal is converted into a gaseous product in the deposit. The synthesis gas can be used for electricity generation, as chemical base material or for the production of petrol. This increases the usability of coal resources tremendously. At present the CCS technologies (carbon capture and storage) are a much discussed alternative to other CO2 abatement techniques like efficiency impovements. The capture and subsequent storage of CO2 in the deposits created by the actual underground gasification process seem to be technically feasible.

Novel process designs to improve the efficiency of postcombustion carbon dioxide capture

NARCIS (Netherlands)

Sanchez Fernandez, E.

2013-01-01

The term carbon dioxide capture and storage (CCS) refers to a range of technologies that can reduce CO2 emissions from fossil fuels enabling the continued use of this fuel type without compromising the security of electricity supply. The technologies applicable to CCS differ in many key aspects; the

Development of Electro-Microbial Carbon Capture and Conversion Systems

KAUST Repository

Al Rowaihi, Israa S.

2017-05-01

Carbon dioxide is a viable resource, if used as a raw material for bioprocessing. It is abundant and can be collected as a byproduct from industrial processes. Globally, photosynthetic organisms utilize around 6’000 TW (terawatt) of solar energy to fix ca. 800 Gt (gigaton) of CO2 in the planets largest carbon-capture process. Photosynthesis combines light harvesting, charge separation, catalytic water splitting, generation of reduction equivalents (NADH), energy (ATP) production and CO2 fixation into one highly interconnected and regulated process. While this simplicity makes photosynthetic production of commodity interesting, yet photosynthesis suffers from low energy efficiency, which translates in an extensive footprint for solar biofuels production conditions that store < 2% of solar energy. Electron transfer processes form the core of photosynthesis. At moderate light intensity, the electron transport chains reach maximum transfer rates and only work when photons are at appropriate wavelengths, rendering the process susceptible to oxidative damage, which leads to photo-inhibition and loss of efficiency. Based on our fundamental analysis of the specialized tasks in photosynthesis, we aimed to optimize the efficiency of these processes separately, then combine them in an artificial photosynthesis (AP) process that surpasses the low efficiency of natural photosynthesis. Therefore, by combining photovoltaic light harvesting with electrolytic water splitting or CO2 reduction in combination with microbiological conversion of electrochemical products to higher valuable compounds, we developed an electro-microbial carbon capture and conversion setups that capture CO2 into the targeted bioplastic; polyhydroxybutyrate (PHB). Based on the type of the electrochemical products, and the microorganism that either (i) convert products formed by electrochemical reduction of CO2, e.g. formate (using inorganic cathodes), or (ii) use electrochemically produced H2 to reduce CO2

About the variation mechanism of the isotopic composition of oxygen and carbon through the geological ages

International Nuclear Information System (INIS)

Torquato, J.R.F.; Frischkorn, H.

1982-01-01

The variations of the Δ 180 ratio found in the carbonates are shown as being of the primary origin. In addition it is shown that these values can be preserved, through the geological ages, even it one considers the carbonates to be worked over again. Are given some subsidies about the study of the paleoenvironments through the analysis of the isotopic composition of the carbon. (A.B.) [pt

CO2 CAPTURE BY ABSORPTION WITH POTASSIUM CARBONATE

Energy Technology Data Exchange (ETDEWEB)

Gary T. Rochelle; A. Frank Seibert; J. Tim Cullinane; Terraun Jones

2003-01-01

The objective of this work is to improve the process for CO{sub 2} capture by alkanolamine absorption/stripping by developing an alternative solvent, aqueous K{sub 2}CO{sub 3} promoted by piperazine. Progress has been made in this reporting period on three subtasks. The rigorous Electrolyte Non-Random Two-Liquid (electrolyte-NRTL) model has been regressed to represent CO{sub 2} solubility in potassium carbonate/bicarbonate solutions. An analytical method for piperazine has been developed using a gas chromatograph. Funding has been obtained and equipment has been donated to provide for modifications of the existing pilot plant system with stainless steel materials.

An integrative approach to the Carbon Capture and Storage (CCS) technologies inside a Water-Energy Nexus Framework

NARCIS (Netherlands)

Vaca Jiménez, Santiago David; Nonhebel, Sanderine; Dijkema, Gerhard

2016-01-01

The energy sector is a major source of the anthropogenic CO2 emissions. Therefore, the sector’s de-carbonization is imperative if we intend to curb the progression of Climate Change. Carbon Capture and Storage (CCS) was created in an attempt to reduce the carbon footprint of energy production.

Comparison of two electrolyte models for the carbon capture with aqueous ammonia

DEFF Research Database (Denmark)

Darde, Victor; Thomsen, Kaj; van Well, Willy J.M.

2012-01-01

Post-combustion carbon capture is attracting much attention due to the fact that it can be retrofitted on existing coal power plants. Among the most interesting technologies is the one that employs aqueous ammonia solutions to absorb the generated carbon dioxide. The evaluation of such process.......2). Subsequently, a simple absorption/regeneration layout is simulated employing both models and the process performances are compared. In general, the Extended UNIQUAC appears to describe the experimental data for larger ranges of temperature, pressure and concentration of ammonia more satisfactorily. The energy...

Geologic map showing springs rich in carbon dioxide or or chloride in California

Science.gov (United States)

Barnes, Ivan; Irwin, William P.; Gibson, H.A.

1975-01-01

Carbon dioxide- and chloride-rich springs occur in all geologic provinces in California, but are most abundant in the Coast Ranges and the Great Valley. The carbon-dioxide-rich springs issue mainly from Franciscan terrane; they also are rich in boron and are of the metamorphic type (White, 1957). Based on isotopic data, either the carbon dioxide or the water, or both, may be of metamorphic origin. Because of high magnesium values, the water of many of the carbon-dioxide-rich springs is thought to have passed through serpentinite. The chloride-rich waters are most common in rocks of the Great Valley sequence. Nearly all are more dilute than present-day sea water. The similarity in isotopic compositions of the metamorphic carbon-dioxide-rich water and the chloride-rich water may indicate a similar extent of water-rock interaction.

Technology Roadmaps: Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2009-07-01

Carbon capture and storage (CCS) is an important part of the lowest-cost greenhouse gas (GHG) mitigation portfolio. IEA analysis suggests that without CCS, overall costs to reduce emissions to 2005 levels by 2050 increase by 70%. This roadmap includes an ambitious CCS growth path in order to achieve this GHG mitigation potential, envisioning 100 projects globally by 2020 and over 3000 projects by 2050. This roadmap's level of project development requires an additional investment of over USD 2.5-3 trillion from 2010 to 2050, which is about 6% of the overall investment needed to achieve a 50% reduction in GHG emissions by 2050. OECD governments will need to increase funding for CCS demonstration projects to an average annual level of USD 3.5 to 4 billion (bn) from 2010 to 2020. In addition, mechanisms need to be established to incentivise commercialisation beyond 2020 in the form of mandates, GHG reduction incentives, tax rebates or other financing mechanisms.

Exploring the potential impact of implementing carbon capture technologies in fossil fuel power plants on regional European water stress index levels

NARCIS (Netherlands)

Schakel, W.B.; Pfister, Stephan; Ramirez, C.A.

Equipping power plants with carbon capture technology can affect cooling demand and water use. This study has explored the potential impact of large scale deployment of power plants with carbon capture technologies on future regional water stress in Europe. A database including 458 of European

Carbon Capture and Sequestration: A Regulatory Gap Assessment

Energy Technology Data Exchange (ETDEWEB)

Lincoln Davies; Kirsten Uchitel; John Ruple; Heather Tanana

2012-04-30

Though a potentially significant climate change mitigation strategy, carbon capture and sequestration (CCS) remains mired in demonstration and development rather than proceeding to full-scale commercialization. Prior studies have suggested numerous reasons for this stagnation. This Report seeks to empirically assess those claims. Using an anonymous opinion survey completed by over 200 individuals involved in CCS, it concludes that there are four primary barriers to CCS commercialization: (1) cost, (2) lack of a carbon price, (3) liability risks, and (4) lack of a comprehensive regulatory regime. These results largely confirm previous work. They also, however, expose a key barrier that prior studies have overlooked: the need for comprehensive, rather than piecemeal, CCS regulation. The survey data clearly show that the CCS community sees this as one of the most needed incentives for CCS deployment. The community also has a relatively clear idea of what that regulation should entail: a cooperative federalism approach that directly addresses liability concerns and that generally does not upset traditional lines of federal-state authority.

Alternative solvents for post combustion carbon capture

Energy Technology Data Exchange (ETDEWEB)

Arachchige, Udara S.P.R. [Telemark University College, Porsgrunn (Norway); Melaaen, Morten C. [Telemark University College, Porsgrunn (Norway); Tel-Tek, Porsgrunn (Norway)

2013-07-01

The process model of post combustion chemical absorption is developed in Aspen Plus for both coal and gas fired power plant flue gas treating. The re-boiler energy requirement is considered as the most important factor to be optimized. Two types of solvents, mono-ethylamine (MEA) and di-ethylamine (DEA), are used to implement the model for three different efficiencies. The re-boiler energy requirement for regeneration process is calculated. Temperature and concentration profiles in absorption column are analyzed to understand the model behavior. Re-boiler energy requirement is considerably lower for DEA than MEA as well as impact of corrosion also less in DEA. Therefore, DEA can be recommended as a better solvent for post combustion process for carbon capture plants in fossil fuel fired power industries.

Capture ready study

Energy Technology Data Exchange (ETDEWEB)

Minchener, A.

2007-07-15

There are a large number of ways in which the capture of carbon as carbon dioxide (CO{sub 2}) can be integrated into fossil fuel power stations, most being applicable for both gas and coal feedstocks. To add to the choice of technology is the question of whether an existing plant should be retrofitted for capture, or whether it is more attractive to build totally new. This miscellany of choices adds considerably to the commercial risk of investing in a large power station. An intermediate stage between the non-capture and full capture state would be advantageous in helping to determine the best way forward and hence reduce those risks. In recent years the term 'carbon capture ready' or 'capture ready' has been coined to describe such an intermediate stage plant and is now widely used. However a detailed and all-encompassing definition of this term has never been published. All fossil fuel consuming plant produce a carbon dioxide gas byproduct. There is a possibility of scrubbing it with an appropriate CO{sub 2} solvent. Hence it could be said that all fossil fuel plant is in a condition for removal of its CO{sub 2} effluent and therefore already in a 'capture ready' state. Evidently, the practical reality of solvent scrubbing could cost more than the rewards offered by such as the ETS (European Trading Scheme). In which case, it can be said that although the possibility exists of capturing CO{sub 2}, it is not a commercially viable option and therefore the plant could not be described as ready for CO{sub 2} capture. The boundary between a capture ready and a non-capture ready condition using this definition cannot be determined in an objective and therefore universally acceptable way and criteria must be found which are less onerous and less potentially contentious to assess. 16 refs., 2 annexes.

Development of a Cl-impregnated activated carbon for entrained-flow capture of elemental mercury.

Science.gov (United States)

Ghorishi, S Behrooz; Keeney, Robert M; Serre, Shannon D; Gullett, Brian K; Jozewicz, Wojciech S

2002-10-15

Efforts to discern the role of an activated carbon's surface functional groups on the adsorption of elemental mercury (Hg0) and mercuric chloride demonstrated that chlorine (Cl) impregnation of a virgin activated carbon using dilute solutions of hydrogen chloride leads to increases (by a factor of 2-3) in fixed-bed capture of these mercury species. A commercially available activated carbon (DARCO FGD, NORITAmericas Inc. [FGD])was Cl-impregnated (Cl-FGD) [5 lb (2.3 kg) per batch] and tested for entrained-flow, short-time-scale capture of Hg0. In an entrained flow reactor, the Cl-FGD was introduced in Hg0-laden flue gases (86 ppb of Hg0) of varied compositions with gas/solid contact times of about 3-4 s, resulting in significant Hg0 removal (80-90%), compared to virgin FGD (10-15%). These levels of Hg0 removal were observed across a wide range of very low carbon-to-mercury weight ratios (1000-5000). Variation of the natural gas combustion flue gas composition, by doping with nitrogen oxides and sulfur dioxide, and the flow reactor temperature (100-200 degrees C) had minimal effects on Hg0 removal bythe Cl-FGD in these carbon-to-mercury weight ratios. These results demonstrate significant enhancement of activated carbon reactivity with minimal treatment and are applicable to combustion facilities equipped with downstream particulate matter removal such as an electrostatic precipitator.

The potential role of natural gas power plants with carbon capture and storage as a bridge to a low-carbon future

Data.gov (United States)

U.S. Environmental Protection Agency — This dataset represents the data underlying the figures presented in the manuscript "The potential role of natural gas power plants with carbon capture and storage...

Capture and geological sequestration of CO{sub 2}: fighting against global warming; Capture et stockage geologique du CO{sub 2}: lutter contre le rechauffement planetaire

Energy Technology Data Exchange (ETDEWEB)

Czernichowski-Lauriol, I

2006-07-01

In order to take up the global warming challenge, a set of emergency measures is to be implemented: energy saving, clean transportation systems, development of renewable energy sources.. CO{sub 2} sequestration of massive industrial emission sources inside deep geologic formations is another promising solution, which can contribute to the division by two of the world CO{sub 2} emissions between today and 2050. The CO{sub 2} capture and sequestration industry is developing. Research projects and pilot facilities are on the increase over the world. Their aim is to warrant the efficiency and security of this technology over the centuries to come. (J.S.)

Carbon Capture and Storage Legal and Regulatory Review. Edition 2

Energy Technology Data Exchange (ETDEWEB)

NONE

2011-07-01

The International Energy Agency (IEA) estimates that 100 carbon capture and storage (CCS) projects must be implemented by 2020 and over 3000 by 2050 if CCS is to fully contribute to the least-cost technology portfolio for CO2 mitigation. To help countries address the many legal and regulatory issues associated with such rapid deployment, the IEA launched the Carbon Capture and Storage Legal and Regulatory Review (CCS Review) in October 2010. The CCS Review gathers contributions by national and regional governments, as well as leading organisations engaged in CCS regulatory activities, to provide a knowledge-sharing forum that supports national-level CCS regulatory development. Each contribution provides a short summary of recent and anticipated developments and highlights a particular regulatory theme (such as financial contributions to long-term stewardship). To introduce each edition, the IEA provides a brief analysis of key advances and trends. Produced bi-annually, the CCS Review provides an up-to-date snapshot of global CCS regulatory developments. The theme for the second edition of the CCS Review, released in May 2011, is long-term liability for stored CO2. Other key issues addressed include: national progress towards implementation of the EU CCS Directive; developments in marine treaties relevant to CCS; international climate change negotiations; and the development process for CCS regulation.

Developments and innovation in carbon dioxide (CO{sub 2}) capture and storage technology. Volume 2: Carbon dioxide (CO{sub 2}) storage and utilisation

Energy Technology Data Exchange (ETDEWEB)

Mercedes Maroto-Valer, M. (ed.)

2010-07-01

This volume initially reviews geological sequestration of CO{sub 2}, from saline aquifer sequestration to oil and gas reservoir and coal bed storage, including coverage of reservoir sealing, and monitoring and modelling techniques used to verify geological sequestration of CO{sub 2}. Terrestrial and ocean sequestration are also reviewed, along with the environmental impact and performance assessments for these routes. The final section reviews advanced concepts for CO{sub 2} storage and utilization, such as industrial utilization, biofixation, mineral carbonation and photocatalytic reduction.

Evaluating the development of carbon capture and storage technologies in the United States

NARCIS (Netherlands)

Alphen, K. van; Noothout, P.M.; Hekkert, M.P.; Turkenburg, W.C.

2010-01-01

Carbon capture and storage (CCS) is seen as an important solution to solve the twin challenge of reducing GHG emissions, while utilizing fossil fuel reserves to meet future energy requirements. In this study an innovation systems perspective is applied to review the development of CCS technologies

Well materials durability in case of carbon dioxide and hydrogen sulphide geological sequestration

International Nuclear Information System (INIS)

Jacquemet, N.

2006-01-01

The geological sequestration of carbon dioxide (CO 2 ) and hydrogen sulphide (H 2 S) is a promising solution for the long-term storage of these undesirable gases. It consists in injecting them via wells into deep geological reservoirs. The steel and cement employed in the well casing can be altered and provide pathways for leakage with subsequent human and environmental consequences. The materials ageing was investigated by laboratory experiments in geologically relevant P-T conditions. A new experimental and analysis procedure was designed for this purpose. A numerical approach was also done. The cement and steel were altered in various fluid phases at 500 bar-120 C and 500 bar-200 C: a brine, a brine saturated with H 2 S-CO 2 , a mixture of brine saturated with H 2 S-CO 2 and of supercritical H 2 S-CO 2 phase, a dry supercritical H 2 S-CO 2 phase without liquid water. In all cases, two distinct reactions are observed: the cement carbonation by the CO 2 and the steel sulfidation by the H 2 S. The carbonation and sulfidation are respectively maximal and minimal when they occur within the dry supercritical phase without liquid water. The textural and porosity properties of the cement are weakly affected by all the treatments at 120 C. The porosity even decreases in presence of H 2 S-CO 2 . But these properties are affected at 200 C when liquid water is present in the system. At this temperature, the initial properties are only preserved or improved by the treatments within the dry supercritical phase. The steel is corroded in all cases and thus is the vulnerable material of the wells. (author)

Activated carbon enhancement with covalent organic polymers: An innovative material for application in water purification and carbon dioxide capture

DEFF Research Database (Denmark)

Mines, Paul D.; Thirion, Damien; Uthuppu, Basil

Covalent organic polymers (COPs) have emerged as one of the leading advanced materials for environmental applications, such as the capture and recovery of carbon dioxide and the removal of contaminants from polluted water.1–4 COPs exhibit many remarkable properties that other leading advanced mat...

Trade-offs in assessing different energy futures: a regional multi-criteria assessment of the role of carbon dioxide capture and storage

International Nuclear Information System (INIS)

Shackley, Simon; McLachlan, Carly

2006-01-01

We examine the responses of stakeholders from the public and private sectors to future energy scenarios for the year 2050 for the North West of England. The main focus of the paper is to examine the stakeholders' reactions to the mitigation option of capturing CO 2 from power stations and storing it in suitable off-shore geological reservoirs. Five energy scenarios were developed which involved a range of levels of CO 2 capture and storage (CCS): Fossilwise, Nuclear Renaissance, Renewable Generation and Spreading the Load high and low scenarios. A multi-criteria assessment method (MCA) was used as a way of elucidating stakeholders' views on the desirability or otherwise of each scenario against nine stakeholder-derived criteria. We found that stakeholders were either business-focused or environment/society-focused with respect to weighting of the criteria. Scoring of the scenarios did not follow such a straightforward pattern. Most respondents scored and weighted strategically and tended to express a clear preference for a form of energy generation. The results suggest that there is unlikely to be a wide-ranging consensus amongst energy stakeholders on the desirability of specific future forms of energy generation. On balance, the results support the inclusion of CCS within scenarios of a low-carbon energy system

CarbonSAFE Illinois - Macon County

Energy Technology Data Exchange (ETDEWEB)

Whittaker, Steve [University of Illinois; Illinois State Geological Survey

2017-08-03

CarbonSAFE Illinois is a a Feasibility study to develop an established geologic storage complex in Macon County, Illinois, for commercial-scale storage of industrially sourced CO2. Feasibility activities are focused on the Mt. Simon Storage Complex; a step-out well will be drilled near existing storage sites (i.e., the Midwest Geological Sequestration Consortium’s Illinois Basin – Decatur Project and the Illinois Industrial Carbon Capture and Storage Project) to further establish commercial viability of this complex and to evaluate EOR potential in a co-located oil-field trend. The Archer Daniels Midland facility (ethanol plant), City Water, Light, and Power in Springfield, Illinois (coal-fired power station), and other regional industries are potential sources of anthropogenic CO2 for storage at this complex. Site feasibility will be evaluated through drilling results, static and dynamic modeling, and quantitative risk assessment. Both studies will entail stakeholder engagement, consideration of infrastructure requirements, existing policy, and business models. Project data will help calibrate the National Risk Assessment Partnership (NRAP) Toolkit to better understand the risks of commercial-scale carbon storage.

N-doped polypyrrole-based porous carbons for CO{sub 2} capture

Energy Technology Data Exchange (ETDEWEB)

Sevilla, Marta; Valle-Vigon, Patricia; Fuertes, Antonio B. [Instituto Nacional del Carbon (CSIC), P.O. Box 73, 33080 Oviedo (Spain)

2011-07-22

Highly porous N-doped carbons have been successfully prepared by using KOH as activating agent and polypyrrole (PPy) as carbon precursor. These materials were investigated as sorbents for CO{sub 2} capture. The activation process was carried out under severe (KOH/PPy = 4) or mild (KOH/PPy = 2) activation conditions at different temperatures in the 600-800 C range. Mildly activated carbons have two important characteristics: i) they contain a large number of nitrogen functional groups (up to 10.1 wt% N) identified as pyridonic-N with a small proportion of pyridinic-N groups, and ii) they exhibit, in relation to the carbons prepared with KOH/PPy = 4, narrower micropore sizes. The combination of both of these properties explains the large CO{sub 2} adsorption capacities of mildly activated carbon. In particular, a very high CO{sub 2} adsorption uptake of 6.2 mmol.g{sup -1} (0 C) was achieved for porous carbons prepared with KOH/PPy = 2 and 600 C (1700 m{sup 2}.g{sup -1}, pore size {approx} 1 nm and 10.1 wt% N. Furthermore, we observed that these porous carbons exhibit high CO{sub 2} adsorption rates, a good selectivity for CO{sub 2}-N{sub 2} separation and it can be easily regenerated. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Thermodynamics of a post combustion hydrate-based carbon dioxide capture process

International Nuclear Information System (INIS)

Ben Attouche Sfaxi, I.

2011-07-01

Hydrates selectivity towards carbon dioxide is offering a promising route for carbon dioxide removal from flue gases. Hydrate-based CO 2 capture process could substitute amine facilities widely implemented in gas treatment plants but suffering from oxidative degradation problems and high energy demand. In the framework of this thesis, we focus on phase equilibria that are involved in such process. Experimental dissociation conditions for clathrate hydrates of carbon dioxide and nitrogen, in the presence of some promoting molecules (Tetrahydrofuran, Tetrabutyl ammonium bromide and Tetrabutyl ammonium Fluoride ) are reported in the experimental section of this work. The data generated in this work along with literature data are compared to the model predictions. The developed model is based on the Cubic Plus Association (CPA) equation of state (EoS) for fluid phases combined to the van der Waals and Platteeuw's theory for the hydrate phase. (author)

Improving Prediction Accuracy of a Rate-Based Model of an MEA-Based Carbon Capture Process for Large-Scale Commercial Deployment

Directory of Open Access Journals (Sweden)

Xiaobo Luo

2017-04-01

Full Text Available Carbon capture and storage (CCS technology will play a critical role in reducing anthropogenic carbon dioxide (CO2 emission from fossil-fired power plants and other energy-intensive processes. However, the increment of energy cost caused by equipping a carbon capture process is the main barrier to its commercial deployment. To reduce the capital and operating costs of carbon capture, great efforts have been made to achieve optimal design and operation through process modeling, simulation, and optimization. Accurate models form an essential foundation for this purpose. This paper presents a study on developing a more accurate rate-based model in Aspen Plus® for the monoethanolamine (MEA-based carbon capture process by multistage model validations. The modeling framework for this process was established first. The steady-state process model was then developed and validated at three stages, which included a thermodynamic model, physical properties calculations, and a process model at the pilot plant scale, covering a wide range of pressures, temperatures, and CO2 loadings. The calculation correlations of liquid density and interfacial area were updated by coding Fortran subroutines in Aspen Plus®. The validation results show that the correlation combination for the thermodynamic model used in this study has higher accuracy than those of three other key publications and the model prediction of the process model has a good agreement with the pilot plant experimental data. A case study was carried out for carbon capture from a 250 MWe combined cycle gas turbine (CCGT power plant. Shorter packing height and lower specific duty were achieved using this accurate model.

Assessing the value of retrofitting cement plants for carbon capture: A case study of a cement plant in Guangdong, China

International Nuclear Information System (INIS)

Liang Xi; Li Jia

2012-01-01

Highlights: ► A techno-economic analysis on retrofitting cement plants to CO 2 capture is conducted. ► A list of criteria is suggested to investigate the CO 2 capture retrofit potential in cement plants. ► The baseline estimated cost of CO 2 avoidance for retrofitting a cement plant is US$70/tCO 2 e. ► The value of retrofit option is US$1.2 million with a 7.3% probability of economic viability. ► The retrofit option value reaches US$20 m with 67% probability under a high carbon price growth. - Abstract: The cement manufacturing sector is the second largest source of anthropogenic greenhouse gas emissions in the world. Carbon Capture and Storage (CCS) is one of the most important technologies to decarbonise the cement manufacturing process. China has accounted for more than half of global cement production since 2008. This study suggests criteria to assess the potential to retrofit cement plants and analyses the economics of retrofitting cement plants for CCS with a case study of a modern dry process cement plant locating in Guangdong province, China. The study assumes the extra heat and power for CO 2 capture and compression is provided by a new 200 MW combined heat and power unit (CHP) (US$17.5/MW h thermal for the cost of coal). The estimated cost of CO 2 avoidance by retrofitting a cement plant for carbon capture in 2012 is US$70/tonne at a 14% discount rate with 25 years remaining lifetime. Through a stochastic cash flow analysis with a real option model and Monte Carlo simulation, the study found the value of an option to retrofit to be US$1.2 million with a 7.3% probability of economic viability. The estimate is very sensitive to the assumptions in the carbon price model (i.e. base carbon price is US$12.00/tCO 2 e in 2012 and the mean growth rate is 8%). The option value and the probability can reach US$20 million and 67% respectively, if a 10% mean carbon price growth is assumed. Compared with post-combustion carbon capture retrofitting prospect in

Calcium and chemical looping technology for power generation and carbon dioxide (CO2) capture solid oxygen- and CO2-carriers

CERN Document Server

Fennell, Paul

2015-01-01

Calcium and Chemical Looping Technology for Power Generation and Carbon Dioxide (CO2) Capture reviews the fundamental principles, systems, oxygen carriers, and carbon dioxide carriers relevant to chemical looping and combustion. Chapters review the market development, economics, and deployment of these systems, also providing detailed information on the variety of materials and processes that will help to shape the future of CO2 capture ready power plants. Reviews the fundamental principles, systems, oxygen carriers, and carbon dioxide carriers relevant to calcium and chemical loopingProvi

Soils and Global Change in the Carbon Cycle over Geological Time

Science.gov (United States)

Retallack, G. J.

2003-12-01

sedimentary rocks; organic matter burial is an important long-term control on CO2 levels in the atmosphere (Berner and Kothavala, 2001). The magnitudes of carbon pools and fluxes involved provide a perspective on the importance of soils compared with other carbon reservoirs ( Figure 1). (6K)Figure 1. Pools and fluxes of reduced carbon (bold) and oxidized carbon (regular) in Gt in the pre-industrial carbon cycle (sources Schidlowski and Aharon, 1992; Siegenthaler and Sarmiento, 1993; Stallard, 1998). Before industrialization, there was only 600 Gt (1 Gt=1015g) of carbon in CO2 and methane in the atmosphere, which is about the same amount as in all terrestrial biomass, but less than half of the reservoir of soil organic carbon. The ocean contained only ˜3 Gt of biomass carbon. The deep ocean and sediments comprised the largest reservoir of bicarbonate and organic matter, but that carbon has been kept out of circulation from the atmosphere for geologically significant periods of time (Schidlowski and Aharon, 1992). Humans have tapped underground reservoirs of fossil fuels, and our other perturbations of the carbon cycle have also been significant ( Vitousek et al., 1997b; see Chapter 8.10).Atmospheric increase of carbon in CO2 to 750 Gt C by deforestation and fossil fuel burning has driven ongoing global warming, but is not quite balanced by changes in the other carbon reservoirs leading to search for a "missing sink" of some 1.8±1.3 GtC, probably in terrestrial organisms, soils, and sediments of the northern hemisphere (Keeling et al., 1982; Siegenthaler and Sarmiento, 1993; Stallard, 1998). Soil organic matter is a big, rapidly cycling reservoir, likely to include much of this missing sink.During the geological past, the sizes of, and fluxes between, these reservoirs have varied enormously as the world has alternated between greenhouse times of high carbon content of the atmosphere, and icehouse times of low carbon content of the atmosphere. Oscillations in the atmospheric

Chemical and Biological Catalytic Enhancement of Weathering of Silicate Minerals and industrial wastes as a Novel Carbon Capture and Storage Technology

Science.gov (United States)

Park, A. H. A.

2014-12-01

Increasing concentration of CO2 in the atmosphere is attributed to rising consumption of fossil fuels around the world. The development of solutions to reduce CO2 emissions to the atmosphere is one of the most urgent needs of today's society. One of the most stable and long-term solutions for storing CO2 is via carbon mineralization, where minerals containing metal oxides of Ca or Mg are reacted with CO2 to produce thermodynamically stable Ca- and Mg-carbonates that are insoluble in water. Carbon mineralization can be carried out in-situ or ex-situ. In the case of in-situ mineralization, the degree of carbonation is thought to be limited by both mineral dissolution and carbonate precipitation reaction kinetics, and must be well understood to predict the ultimate fate of CO2 within geological reservoirs. While the kinetics of in-situ mineral trapping via carbonation is naturally slow, it can be enhanced at high temperature and high partial pressure of CO2. The addition of weak organic acids produced from food waste has also been shown to enhance mineral weathering kinetics. In the case of the ex-situ carbon mineralization, the role of these ligand-bearing organic acids can be further amplified for silicate mineral dissolution. Unfortunately, high mineral dissolution rates often lead to the formation of a silica-rich passivation layer on the surface of silicate minerals. Thus, the use of novel solvent mixture that allows chemically catalyzed removal of this passivation layer during enhanced Mg-leaching surface reaction has been proposed and demonstrated. Furthermore, an engineered biological catalyst, carbonic anhydrase, has been developed and evaluated to accelerate the hydration of CO2, which is another potentially rate-limiting step of the carbonation reaction. The development of these novel catalytic reaction schemes has significantly improved the overall efficiency and sustainability of in-situ and ex-situ mineral carbonation technologies and allowed direct

Geologic assessment of undiscovered oil and gas resources in Aptian carbonates, onshore northern Gulf of Mexico Basin, United States

Science.gov (United States)

Hackley, Paul C.; Karlsen, Alexander W.

2014-01-01

Carbonate lithofacies of the Lower Cretaceous Sligo Formation and James Limestone were regionally evaluated using established U.S. Geological Survey (USGS) assessment methodology for undiscovered conventional hydrocarbon resources. The assessed area is within the Upper Jurassic–Cretaceous–Tertiary Composite total petroleum system, which was defined for the assessment. Hydrocarbons reservoired in carbonate platform Sligo-James oil and gas accumulations are interpreted to originate primarily from the Jurassic Smackover Formation. Emplacement of hydrocarbons occurred via vertical migration along fault systems; long-range lateral migration also may have occurred in some locations. Primary reservoir facies include porous patch reefs developed over paleostructural salt highs, carbonate shoals, and stacked linear reefs at the carbonate shelf margin. Hydrocarbon traps dominantly are combination structural-stratigraphic. Sealing lithologies include micrite, calcareous shale, and argillaceous lime mudstone. A geologic model, supported by discovery history analysis of petroleum geology data, was used to define a single regional assessment unit (AU) for conventional reservoirs in carbonate facies of the Sligo Formation and James Limestone. The AU is formally entitled Sligo-James Carbonate Platform Oil and Gas (50490121). A fully risked mean undiscovered technically recoverable resource in the AU of 50 million barrels of oil (MMBO), 791 billion cubic feet of natural gas (BCFG), and 26 million barrels of natural gas liquids was estimated. Substantial new development through horizontal drilling has occurred since the time of this assessment (2010), resulting in cumulative production of >200 BCFG and >1 MMBO.

Hydrogen production by reforming of fossil and biomass fuels accompanied by carbon dioxide capture process is the energy source for the near future

International Nuclear Information System (INIS)

Aboudheir, Ahmed; Idem, Raphael; Tontiwachwuthikul, Paitoon; Wilson, Malcolm; Kambietz, Lionel

2006-01-01

Hydrogen has a significant future potential as an alternative energy source for the transportation sector as well as in residential homes and offices, H 2 in fuel cell power systems provides an alternative to direct fossil fuel and biomass combustion based technologies and offer the possibility for a significant reduction in greenhouse gas emission based on improved H 2 yield per unit of fossil fuel and biomass, compatibility with renewable energies and motivation to convert to a H 2 -based energy economy. Several practical techniques for H 2 production to service H 2 refuelling stations as well as homes and offices, all of which need to be located at the end of the energy distribution network, include: (1) the carbon dioxide reforming of natural gas; (2) reforming of gasoline; (3) reforming of crude ethanol. Locating the H 2 production at the end of the energy distribution network solves the well-known problems of metal fatigue and high cost of H 2 compression for long distance transportation if H 2 is produced in a large centralized plant. In addition, the ratification of the Kyoto Protocol and the need to reduce emissions of CO 2 to the atmosphere has prompted the capture and utilization of the CO 2 produced from the reforming process. In this research: (1) new efficient catalysts for each reforming process was developed; (2) a new efficient catalyst for our version of the water gas shift reaction to convert carbon monoxide to carbon dioxide was developed; (3) a new membrane separation process for production of high purity, fuel cell-grade H 2 was designed; (4) a numerical model for optimum process design and optimum utilization of resources both at the laboratory and industrial scales was developed; (5) various processes for CO 2 capture were investigated experimentally in order to achieve a net improvement in the absorption process; (6) the utilization of captured CO 2 for enhanced oil recovery and/or storage in an aging oil field were investigated; (7

Sulfation of CaO particles in a carbonation/calcination loop to capture CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Grasa, G.S.; Alonso, M.; Abanades, J.C. [CSIC, Zaragoza (Spain)

2008-03-15

CaO is being proposed as a regenerable sorbent of CO{sub 2} via a carbonation/calcination loop. It is well known that natural sorbents lose their capacity to capture CO{sub 2} with the number of cycles due to textural degradation. In coal combustion systems, reaction with the SO{sub 2} present in flue gases also causes sorbent deactivation. This work investigates the effect of partial sorbent sulfation on the amount of CaO used in systems where both carbonation and sulfation reactions are competing. We have found that SO{sub 2} reacts with the deactivated CaO resulting from repetitive calcination/carbonation reactions. Therefore, the deactivation of CaO as a result of the presence of SO{sub 2} is lower than one would expect if one assumes that SO{sub 2} reacts only with active CaO. This work shows that changes in the texture of the sorbent due to repetitive carbonation/calcination cycles tend to increase the sulfation capacity of the sorbents tested. This suggests that the purge of deactivated CaO obtained from a CO{sub 2} capture loop could be a more effective sorbent of SO{sub 2} than fresh CaO.

Selectivity and limitations of carbon sorption tubes for capturing siloxanes in biogas during field sampling.

Science.gov (United States)

Tansel, Berrin; Surita, Sharon C

2016-06-01

Siloxane levels in biogas can jeopardize the warranties of the engines used at the biogas to energy facilities. The chemical structure of siloxanes consists of silicon and oxygen atoms, alternating in position, with hydrocarbon groups attached to the silicon side chain. Siloxanes can be either in cyclic (D) or linear (L) configuration and referred with a letter corresponding to their structure followed by a number corresponding to the number of silicon atoms present. When siloxanes are burned, the hydrocarbon fraction is lost and silicon is converted to silicates. The purpose of this study was to evaluate the adequacy of activated carbon gas samplers for quantitative analysis of siloxanes in biogas samples. Biogas samples were collected from a landfill and an anaerobic digester using multiple carbon sorbent tubes assembled in series. One set of samples was collected for 30min (sampling 6-L gas), and the second set was collected for 60min (sampling 12-L gas). Carbon particles were thermally desorbed and analyzed by Gas Chromatography Mass Spectrometry (GC/MS). The results showed that biogas sampling using a single tube would not adequately capture octamethyltrisiloxane (L3), hexamethylcyclotrisiloxane (D3), octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6). Even with 4 tubes were used in series, D5 was not captured effectively. The single sorbent tube sampling method was adequate only for capturing trimethylsilanol (TMS) and hexamethyldisiloxane (L2). Affinity of siloxanes for activated carbon decreased with increasing molecular weight. Using multiple carbon sorbent tubes in series can be an appropriate method for developing a standard procedure for determining siloxane levels for low molecular weight siloxanes (up to D3). Appropriate quality assurance and quality control procedures should be developed for adequately quantifying the levels of the higher molecular weight siloxanes in biogas with sorbent tubes

Deliberative decarbonisation? Assessing the potential of an ethical governance framework for low-carbon energy through the case of carbon dioxide capture and storage

OpenAIRE

Leslie Mabon; Simon Shackley; Samuela Vercelli; Jonathan Anderlucci; Kelvin Boot

2015-01-01

In this paper we explore the potential of a framework of ethical governance for low-carbon energy. Developing mainly in the field of information and communications technology, ethical governance is concerned with the marginalisation of ethical and moral issues during development and deployment of new technologies. Focusing on early carbon dioxide capture and storage (CCS) projects, we argue that a focus on technical arguments in the governance of low-carbon energy similarly risks sidelining d...

Carbon capture from natural gas using multi-walled CNTs based mixed matrix membranes.

Science.gov (United States)

Hussain, Abid; Farrukh, Sarah; Hussain, Arshad; Ayoub, Muhammad

2017-12-05

Most of the polymers and their blends, utilized in carbon capture membranes, are costly, but cellulose acetate (CA) being inexpensive is a lucrative choice. In this research, pure and mixed matrix membranes (MMMs) have been fabricated to capture carbon from natural gas. Polyethylene glycol (PEG) has been utilized in the fabrication of membranes to modify the chain flexibility of polymers. Multi-walled carbon nanotubes (MWCNTs) provide mechanical strength, thermal stability, an extra free path for CO 2 molecules and augment CO 2 /CH 4 selectivity. Membranes of pure CA, CA/PEG blend of different PEG concentrations (5%, 10%, 15%) and CA/PEG/MWCNTs blend of 10% PEG with different MWCNTs concentrations (5%, 10%, 15%) were prepared in acetone using solution casting techniques. Fabricated membranes were characterized using SEM, TGA and tensile testing. Permeation results revealed remarkable improvement in CO 2 /CH 4 selectivity. In single gas experiments, CO 2 /CH 4 selectivity is enhanced 8 times for pure membranes containing 10% PEG and 14 times for MMMs containing 10% MWCNTs. In mix gas experiments, the CO 2 /CH 4 selectivity is increased 13 times for 10% PEG and 18 times for MMMs with 10% MWCNTs. Fabricated MMMs have a tensile strength of 13 MPa and are more thermally stable than CA membranes.

International Collaboration: the Virtuous Cycle of Low Carbon Innovation and Diffusion. An Analysis of Solar Photovoltaic, Concentrating Solar Power and Carbon Capture and Storage

International Nuclear Information System (INIS)

Dominique, Katheen

2010-01-01

International collaboration can be leveraged to accelerate the innovation and diffusion of low carbon technologies required to realize the shift to a low carbon trajectory. A collaborative approach to innovation has the potential to capture several benefits, including: pooling risks and achieving scale; knowledge sharing that accommodates competition and cooperation; the creation of a global market; facilitation of policy learning and exchange; and the alignment of technology, finance and policy. International Collaboration: the Virtuous Cycle of Low Carbon Innovation and Diffusion An Analysis of Solar Photovoltaic, Concentrating Solar Power and Carbon Capture and Storage A range of obstacles to the diffusion of low carbon technologies provides ample opportunity for international collaboration in global market creation and capacity building, expanding beyond conventional modes of technology transfer. Current collaborative efforts for carbon capture and storage, solar photovoltaic and concentrating solar power technologies are active in all stages of innovation and diffusion and involve a wide range of actors. Yet, current efforts are not sufficient to achieve the necessary level of emission mitigation at the pace required to avoid catastrophic levels of atmospheric destabilization. This analysis sets forth recommendation to scale up current endeavors and create new ones. The analysis begins by describing the fundamental characteristics of innovation and diffusion processes that create opportunities for international collaboration. It then illustrates a broad array of on-going collaborative activities, depicting how these efforts contribute to innovation and diffusion. Finally, highlighting the gap between the current level of collaborative activities and technology targets deemed critical for emission mitigation, the report sets forth several recommendations to build on current efforts and construct new endeavors

Valuing Metal-Organic Frameworks for Postcombustion Carbon Capture: A Benchmark Study for Evaluating Physical Adsorbents

KAUST Repository

Adil, Karim; Bhatt, Prashant; Belmabkhout, Youssef; Abtab, Sk Md Towsif; Jiang, Hao; Assen, Ayalew Hussen Assen; Mallick, Arijit; Cadiau, Amandine; Aqil, Jamal; Eddaoudi, Mohamed

2017-01-01

The development of practical solutions for the energy-efficient capture of carbon dioxide is of prime importance and continues to attract intensive research interest. Conceivably, the implementation of adsorption-based processes using different

Global Action to Advance Carbon Capture and Storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2013-06-01

Representing one-fifth of total global CO2 emissions currently, industrial sectors such as cement, iron and steel, chemicals and refining are expected to emit even more CO2 over the coming decades. Carbon capture and storage (CCS) is currently the only large-scale mitigation option available to cut the emissions intensity of production by over 50% in these sectors. CCS is already proven in some industrial sectors, such as natural gas processing. Yet, the commercial-scale demonstration stage in key sectors such as iron and steel, cement or some processes in the refining sector has not been reached. To achieve decarbonisation goals, policy makers must pay more attention to industrial applications of CCS, while not undermining the global competitiveness of these sectors.

The National Carbon Capture Center at the Power Systems Development Facility

Energy Technology Data Exchange (ETDEWEB)

None, None

2014-07-14

The Power Systems Development Facility (PSDF) is a state-of-the-art test center sponsored by the U.S. Department of Energy (DOE) and dedicated to the advancement of clean coal technology. In addition to the development of high efficiency coal gasification processes, the PSDF features the National Carbon Capture Center (NCCC) to promote new technologies for CO2 capture from coal-derived flue gas and syngas. The NCCC includes multiple, adaptable test skids that allow technology development of CO2 capture concepts using coal-derived flue gas and syngas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity and accelerate their development paths to commercialization. During the calendar year 2013 portion of the Budget Period Four reporting period, efforts at the NCCC focused on post-combustion CO2 capture, gasification, and pre-combustion CO2 capture technology testing. Preparations for future testing were on-going as well, and involved facility upgrades and collaboration with numerous technology developers. In the area of post-combustion, testing was conducted on an enzyme-based technology, advanced solvents from two major developers, and a gas separation membrane. During the year, the gasification process was operated for three test runs, supporting development of water-gas shift and COS hydrolysis catalysts, a mercury sorbent, and several gasification support technologies. Syngas produced during gasification operation was also used for pre-combustion capture technologies, including gas separation membranes from three different technology developers, a CO2 sorbent, and CO2 solvents.

Hydroquinone and quinone-grafted porous carbons for highly selective CO2 capture from flue gases and natural gas upgrading

NARCIS (Netherlands)

Wang, J.; Krishna, R.; Yang, J.; Deng, S.

2015-01-01

Hydroquinone and quinone functional groups were grafted onto a hierarchical porous carbon framework via the Friedel-Crafts reaction to develop more efficient adsorbents for the selective capture and removal of carbon dioxide from flue gases and natural gas. The oxygen-doped porous carbons were

Predicting long-term performance of engineered geologic carbon dioxide storage systems to inform decisions amidst uncertainty

Science.gov (United States)

Pawar, R.

2016-12-01

Risk assessment and risk management of engineered geologic CO2 storage systems is an area of active investigation. The potential geologic CO2 storage systems currently under consideration are inherently heterogeneous and have limited to no characterization data. Effective risk management decisions to ensure safe, long-term CO2 storage requires assessing and quantifying risks while taking into account the uncertainties in a storage site's characteristics. The key decisions are typically related to definition of area of review, effective monitoring strategy and monitoring duration, potential of leakage and associated impacts, etc. A quantitative methodology for predicting a sequestration site's long-term performance is critical for making key decisions necessary for successful deployment of commercial scale geologic storage projects where projects will require quantitative assessments of potential long-term liabilities. An integrated assessment modeling (IAM) paradigm which treats a geologic CO2 storage site as a system made up of various linked subsystems can be used to predict long-term performance. The subsystems include storage reservoir, seals, potential leakage pathways (such as wellbores, natural fractures/faults) and receptors (such as shallow groundwater aquifers). CO2 movement within each of the subsystems and resulting interactions are captured through reduced order models (ROMs). The ROMs capture the complex physical/chemical interactions resulting due to CO2 movement and interactions but are computationally extremely efficient. The computational efficiency allows for performing Monte Carlo simulations necessary for quantitative probabilistic risk assessment. We have used the IAM to predict long-term performance of geologic CO2 sequestration systems and to answer questions related to probability of leakage of CO2 through wellbores, impact of CO2/brine leakage into shallow aquifer, etc. Answers to such questions are critical in making key risk management

Mountaineer Commercial Scale Carbon Capture and Storage Project Topical Report: Preliminary Public Design Report

Energy Technology Data Exchange (ETDEWEB)

Guy Cerimele

2011-09-30

This Preliminary Public Design Report consolidates for public use nonproprietary design information on the Mountaineer Commercial Scale Carbon Capture & Storage project. The report is based on the preliminary design information developed during the Phase I - Project Definition Phase, spanning the time period of February 1, 2010 through September 30, 2011. The report includes descriptions and/or discussions for: (1) DOE's Clean Coal Power Initiative, overall project & Phase I objectives, and the historical evolution of DOE and American Electric Power (AEP) sponsored projects leading to the current project; (2) Alstom's Chilled Ammonia Process (CAP) carbon capture retrofit technology and the carbon storage and monitoring system; (3) AEP's retrofit approach in terms of plant operational and integration philosophy; (4) The process island equipment and balance of plant systems for the CAP technology; (5) The carbon storage system, addressing injection wells, monitoring wells, system monitoring and controls logic philosophy; (6) Overall project estimate that includes the overnight cost estimate, cost escalation for future year expenditures, and major project risks that factored into the development of the risk based contingency; and (7) AEP's decision to suspend further work on the project at the end of Phase I, notwithstanding its assessment that the Alstom CAP technology is ready for commercial demonstration at the intended scale.

Big Sky Carbon Sequestration Partnership

Energy Technology Data Exchange (ETDEWEB)

Susan M. Capalbo

2005-11-01

Partnership region, and to design a risk/cost effectiveness framework to make comparative assessments of each viable sink, taking into account economic costs, offsetting benefits, scale of sequestration opportunities, spatial and time dimensions, environmental risks, and long-term viability. Scientifically sound MMV is critical for public acceptance of these technologies. Deliverables for the 7th Quarter reporting period include (1) for the geological efforts: Reports on Technology Needs and Action Plan on the Evaluation of Geological Sinks and Pilot Project Deployment (Deliverables 2 and 3), and Report on the Feasibility of Mineralization Trapping in the Snake River Plain Basin (Deliverable 14); (2) for the terrestrial efforts: Report on the Evaluation of Terrestrial Sinks and a Report of the Best Production Practices for Soil C Sequestration (Deliverables 8 and 15). In addition, the 7th Quarter activities for the Partnership included further development of the proposed activities for the deployment and demonstration phase of the carbon sequestration pilots including geological and terrestrial pilots, expansion of the Partnership to encompass regions and institutions that are complimentary to the steps we have identified, building greater collaborations with industry and stakeholders in the region, contributed to outreach efforts that spanned all partnerships, co-authorship on the Carbon Capture and Separation report, and developed a regional basis to address future energy opportunities in the region. The deliverables and activities are discussed in the following sections and appended to this report. The education and outreach efforts have resulted in a comprehensive plan which serves as a guide for implementing the outreach activities under Phase I. The public website has been expanded and integrated with the GIS carbon atlas. We have made presentations to stakeholders and policy makers including two tribal sequestration workshops, and made connections to other federal and

2nd clean coal & carbon capture - securing the future. Conference documentation and delegate information

Energy Technology Data Exchange (ETDEWEB)

NONE

2007-07-01

The presentations covered: policies and the regulatory environment - creating opportunities for clean coal technologies; mastering the economics of clean coal - gaining finance and investment for key projects; international initiatives in clean coal technologies; power plant developments; broader uses for coal; and carbon capture and storage.

Systematic framework for carbon dioxide capture and utilization processes to reduce the global carbon dioxide emissions

DEFF Research Database (Denmark)

Frauzem, Rebecca; Plaza, Cristina Calvera; Gani, Rafiqul

information-data on various carbon dioxide emission sources and available capture-utilization technologies; the model and solution libraries [2]; and the generic 3-stage approach for determining more sustainable solutions [3] through superstructure (processing networks) based optimization – adopted for global...... need to provide, amongst other options: useful data from in-house databases on carbon dioxide emission sources; mathematical models from a library of process-property models; numerical solvers from library of implemented solvers; and, work-flows and data-flows for different benefit scenarios...... to be investigated. It is useful to start by developing a prototype framework and then augmenting its application range by increasing the contents of its databases, libraries and work-flows and data-flows. The objective is to present such a prototype framework with its implemented database containing collected...

Low Cost, High Capacity Regenerable Sorbent for Carbon Dioxide Capture from Existing Coal-fired Power Plants

Energy Technology Data Exchange (ETDEWEB)

Alptekin, Gokhan [TDA Research, Inc., Wheat Ridge, CO (United States); Jayaraman, Ambalavanan [TDA Research, Inc., Wheat Ridge, CO (United States); Dietz, Steven [TDA Research, Inc., Wheat Ridge, CO (United States)

2016-03-03

In this project TDA Research, Inc (TDA) has developed a new post combustion carbon capture technology based on a vacuum swing adsorption system that uses a steam purge and demonstrated its technical feasibility and economic viability in laboratory-scale tests and tests in actual coal derived flue gas. TDA uses an advanced physical adsorbent to selectively remove CO₂ from the flue gas. The sorbent exhibits a much higher affinity for CO₂ than N₂, H₂O or O₂, enabling effective CO₂ separation from the flue gas. We also carried out a detailed process design and analysis of the new system as part of both sub-critical and super-critical pulverized coal fired power plants. The new technology uses a low cost, high capacity adsorbent that selectively removes CO₂ in the presence of moisture at the flue gas temperature without a need for significant cooling of the flue gas or moisture removal. The sorbent is based on a TDA proprietary mesoporous carbon that consists of surface functionalized groups that remove CO₂ via physical adsorption. The high surface area and favorable porosity of the sorbent also provides a unique platform to introduce additional functionality, such as active groups to remove trace metals (e.g., Hg, As). In collaboration with the Advanced Power and Energy Program of the University of California, Irvine (UCI), TDA developed system simulation models using Aspen PlusTM simulation software to assess the economic viability of TDA’s VSA-based post-combustion carbon capture technology. The levelized cost of electricity including the TS&M costs for CO₂ is calculated as $116.71/MWh and $113.76/MWh for TDA system integrated with sub-critical and super-critical pulverized coal fired power plants; much lower than the $153.03/MWhand $147.44/MWh calculated for the corresponding amine based systems. The cost of CO₂ captured for TDA’s VSA based system is $38

Oxyfuel carbonation/calcination cycle for low cost CO2 capture in existing power plants

International Nuclear Information System (INIS)

Romeo, Luis M.; Abanades, J. Carlos; Escosa, Jesus M.; Pano, Jara; Gimenez, Antonio; Sanchez-Biezma, Andres; Ballesteros, Juan C.

2008-01-01

Postcombustion CO 2 capture is the best suitable capture technology for existing coal power plants. This paper focuses on an emerging technology that involves the separation of CO 2 using the reversible carbonation reaction of CaO to capture CO 2 from the flue gas, and the calcination of CaCO 3 to regenerate the sorbent and produce concentrated CO 2 for storage. We describe the application to this concept to an existing (with today's technology) power plant. The added capture system incorporates a new supercritical steam cycle to take advantage of the large amount of heat coming out from the high temperature capture process (oxyfired combustion of coal is needed in the CaCO 3 calciner). In these conditions, the capture system is able to generate additional power (26.7% efficiency respect to LHV coal input to the calciner after accounting for all the penalties in the overall system), without disturbing the steam cycle of the reference plant (that retains its 44.9 efficiency). A preliminary cost study of the overall system, using well established analogues in the open literature for the main components, yields capture cost around 16 Euro /ton CO 2 avoided and incremental cost of electricity of just over 1 Euro /MW h e

Cleaner fossil power generation in the 21st century: a technology strategy for carbon capture and storage

Energy Technology Data Exchange (ETDEWEB)

NONE

2009-04-15

The document describes how the research, development and demonstration (RD&D) components of the United Kingdom Government's Carbon Abatement Technologies (CATs) Strategy should be developed and extended, with particular reference to a 2020 target for carbon dioxide capture and storage (CCS) commercialisation and the 2050 UK Committee on Climate Change (CCC) dioxide target. It sets out a strategy for RD&D through the establishment of a collaborative programme linking industry, and academia, and involving different funding sources. The proposed RD& D programme has seven strategic themes: Power plant: focus on cost, increasing efficiency, biomass co-firing; Capture technologies: focus on cost, efficiency penalty, waste heat utilisation; storage: focus on security, monitoring and verification; transport: focus on logistics and transport network; whole system: focus on risks, transient capability, economics, environmental issues; advanced and novel capture technologies; and underpinning technology support. 11 refs., 10 figs., 15 tabs.

An overview of CAFE credits and incorporation of the benefits of on-board carbon capture.

Science.gov (United States)

2014-05-01

This report discusses the application of Corporate Average Fuel Economy (CAFE) : credits that are currently available to vehicle manufacturers in the U.S., and the implications of : on-board carbon capture and sequestration (on-board CCS) on fu...

Carbon capture in vehicles : a review of general support, available mechanisms, and consumer-acceptance issues.

Science.gov (United States)

2012-05-01

This survey of the feasibility of introducing carbon capture and storage (CCS) into light vehicles : started by reviewing the level of international support for CCS in general. While there have been : encouraging signs that CCS is gaining acceptance ...

Pilot project at Hazira, India, for capture of carbon dioxide and its biofixation using microalgae.

Science.gov (United States)

Yadav, Anant; Choudhary, Piyush; Atri, Neelam; Teir, Sebastian; Mutnuri, Srikanth

2016-11-01

The objective of the present study was to set up a small-scale pilot reactor at ONGC Hazira, Surat, for capturing CO 2 from vent gas. The studies were carried out for CO 2 capture by either using microalgae Chlorella sp. or a consortium of microalgae (Scenedesmus quadricauda, Chlorella vulgaris and Chlorococcum humicola). The biomass harvested was used for anaerobic digestion to produce biogas. The carbonation column was able to decrease the average 34 vol.% of CO 2 in vent gas to 15 vol.% of CO 2 in the outlet gas of the carbonation column. The yield of Chlorella sp. was found to be 18 g/m 2 /day. The methane yield was 386 l CH 4 /kg VS fed of Chlorella sp. whereas 228 l CH 4 /kg VS fed of the consortium of algae.

Geological storage of carbon dioxide: the role of sedimentary basins

International Nuclear Information System (INIS)

Gunter, W.D.; Bachu, S.

2001-01-01

Sedimentary basins, occuring throughout the world, are thick piles of geologically deposited sediments that are the hosts for fossil fuel deposits. They may become even more important in the future if their large storage capacity is utilized for disposing of carbon dioxide. Sedimentary basins are dynamic, in the sense that they have an intricate plumbing system defined by the location of high and low permeability strata that control the flow of fluids throughout the basins and define 'hydrogeological' traps. The most secure type of hydrogeological trapping is found in oil and gas reservoirs in the form of 'structural' or 'stratigraphic' traps, termed 'closed' hydrogeological traps which have held oil and gas for millions of years. Obviously, these would be very attractive for CO 2 storage due to their long history of containment. A second type of hydrogeological trapping has been recognized in aquifers of sedimentary basins that have slow flow rates. The pore space in such 'open' hydrogeological traps is usually filled with saline ground or formation water. A volume of CO 2 injected into a deep open hydrogeological trap can take over a million years to travel updip to reach the surface and be released to the atmosphere. Although the capacity of structural/stratigraphic traps for CO 2 storage is small relative to open hydrogeological traps in deep sedimentary basins, they are likely to be used first as they are known to be secure, having held oil and gas for geological time. As the capacity of closed traps is exhausted and more is learned about geochemical trapping, the large storage capacity available in open hydrogeological traps will be utilized where security of the geological storage of CO 2 can be enhanced by geochemical reactions of the CO 2 with basic silicate minerals to form carbonates. Potential short circuits to the surface through faults or abandoned wells must be located and their stability evaluated before injection of CO 2 . In any event, a

Annual Report: Carbon Capture Simulation Initiative (CCSI) (30 September 2013)

Energy Technology Data Exchange (ETDEWEB)

Miller, David C. [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Syamlal, Madhava [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Cottrell, Roger [URS Corporation. (URS), San Francisco, CA (United States); National Energy Technology Lab. (NETL), Morgantown, WV (United States); Kress, Joel D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Sundaresan, S. [Princeton Univ., NJ (United States); Sun, Xin [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Storlie, C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Bhattacharyya, D. [West Virginia Univ., Morgantown, WV (United States); National Energy Technology Lab. (NETL), Morgantown, WV (United States); Tong, Charles [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zitney, Stephen E [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Dale, Crystal [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Engel, Dave [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Agarwal, Deb [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Calafiura, Paolo [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Shinn, John [SynPatEco, Pleasant Hill, CA (United States)

2013-09-30

The Carbon Capture Simulation Initiative (CCSI) is a partnership among national laboratories, industry and academic institutions that is developing and deploying state-of-the-art computational modeling and simulation tools to accelerate the commercialization of carbon capture technologies from discovery to development, demonstration, and ultimately the widespread deployment to hundreds of power plants. The CCSI Toolset will provide end users in industry with a comprehensive, integrated suite of scientifically validated models, with uncertainty quantification (UQ), optimization, risk analysis and decision making capabilities. The CCSI Toolset incorporates commercial and open-source software currently in use by industry and is also developing new software tools as necessary to fill technology gaps identified during execution of the project. Ultimately, the CCSI Toolset will (1) enable promising concepts to be more quickly identified through rapid computational screening of devices and processes; (2) reduce the time to design and troubleshoot new devices and processes; (3) quantify the technical risk in taking technology from laboratory-scale to commercial-scale; and (4) stabilize deployment costs more quickly by replacing some of the physical operational tests with virtual power plant simulations. CCSI is led by the National Energy Technology Laboratory (NETL) and leverages the Department of Energy (DOE) national laboratories’ core strengths in modeling and simulation, bringing together the best capabilities at NETL, Los Alamos National Laboratory (LANL), Lawrence Berkeley National Laboratory (LBNL), Lawrence Livermore National Laboratory (LLNL), and Pacific Northwest National Laboratory (PNNL). The CCSI’s industrial partners provide representation from the power generation industry, equipment manufacturers, technology providers and engineering and construction firms. The CCSI’s academic participants (Carnegie Mellon University, Princeton University, West

Can Thermally Sprayed Aluminum (TSA) Mitigate Corrosion of Carbon Steel in Carbon Capture and Storage (CCS) Environments?

Science.gov (United States)

Paul, S.; Syrek-Gerstenkorn, B.

2017-01-01

Transport of CO2 for carbon capture and storage (CCS) uses low-cost carbon steel pipelines owing to their negligible corrosion rates in dry CO2. However, in the presence of liquid water, CO2 forms corrosive carbonic acid. In order to mitigate wet CO2 corrosion, use of expensive corrosion-resistant alloys is recommended; however, the increased cost makes such selection economically unfeasible; hence, new corrosion mitigation methods are sought. One such method is the use of thermally sprayed aluminum (TSA), which has been used to mitigate corrosion of carbon steel in seawater, but there are concerns regarding its suitability in CO2-containing solutions. A 30-day test was carried out during which carbon steel specimens arc-sprayed with aluminum were immersed in deionized water at ambient temperature bubbled with 0.1 MPa CO2. The acidity (pH) and potential were continuously monitored, and the amount of dissolved Al3+ ions was measured after completion of the test. Some dissolution of TSA occurred in the test solution leading to nominal loss in coating thickness. Potential measurements revealed that polarity reversal occurs during the initial stages of exposure which could lead to preferential dissolution of carbon steel in the case of coating damage. Thus, one needs to be careful while using TSA in CCS environments.

Final Deliverable W6, D6.4: Coal power plants with carbon capture and storage – A sustainability assessment

NARCIS (Netherlands)

Ramirez, C.A.; Schakel, W.B.; Wood, R.; Grytli, T.

2013-01-01

Carbon Capture and Storage (CCS) is increasingly gaining attention as a strategy for the abatement of greenhouse gas (GHG) emissions. CCS includes the capture of CO2 emissions from electricity generation plants and/or industrial processes, its transport (by pipeline or ships) and sequestration in

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents

Energy Technology Data Exchange (ETDEWEB)

Thomas Nelson; David Green; Paul Box; Raghubir Gupta; Gennar Henningsen

2007-06-30

Regenerable sorbents based on sodium carbonate (Na{sub 2}CO{sub 3}) can be used to separate carbon dioxide (CO{sub 2}) from coal-fired power plant flue gas. Upon thermal regeneration and condensation of water vapor, CO{sub 2} is released in a concentrated form that is suitable for reuse or sequestration. During the research project described in this report, the technical feasibility and economic viability of a thermal-swing CO{sub 2} separation process based on dry, regenerable, carbonate sorbents was confirmed. This process was designated as RTI's Dry Carbonate Process. RTI tested the Dry Carbonate Process through various research phases including thermogravimetric analysis (TGA); bench-scale fixed-bed, bench-scale fluidized-bed, bench-scale co-current downflow reactor testing; pilot-scale entrained-bed testing; and bench-scale demonstration testing with actual coal-fired flue gas. All phases of testing showed the feasibility of the process to capture greater than 90% of the CO{sub 2} present in coal-fired flue gas. Attrition-resistant sorbents were developed, and these sorbents were found to retain their CO{sub 2} removal activity through multiple cycles of adsorption and regeneration. The sodium carbonate-based sorbents developed by RTI react with CO{sub 2} and water vapor at temperatures below 80 C to form sodium bicarbonate (NaHCO3) and/or Wegscheider's salt. This reaction is reversed at temperatures greater than 120 C to release an equimolar mixture of CO{sub 2} and water vapor. After condensation of the water, a pure CO{sub 2} stream can be obtained. TGA testing showed that the Na{sub 2}CO3 sorbents react irreversibly with sulfur dioxide (SO{sub 2}) and hydrogen chloride (HCl) (at the operating conditions for this process). Trace levels of these contaminants are expected to be present in desulfurized flue gas. The sorbents did not collect detectable quantities of mercury (Hg). A process was designed for the Na{sub 2}CO{sub 3}-based sorbent that

Greening coal: breakthroughs and challenges in carbon capture and storage.

Science.gov (United States)

Stauffer, Philip H; Keating, Gordon N; Middleton, Richard S; Viswanathan, Hari S; Berchtold, Kathryn A; Singh, Rajinder P; Pawar, Rajesh J; Mancino, Anthony

2011-10-15

Like it or not, coal is here to stay, for the next few decades at least. Continued use of coal in this age of growing greenhouse gas controls will require removing carbon dioxide from the coal waste stream. We already remove toxicants such as sulfur dioxide and mercury, and the removal of CO₂ is the next step in reducing the environmental impacts of using coal as an energy source (i.e., greening coal). This paper outlines some of the complexities encountered in capturing CO₂ from coal, transporting it large distances through pipelines, and storing it safely underground.

Highly integrated CO2 capture and conversion: Direct synthesis of cyclic carbonates from industrial flue gas

KAUST Repository

Barthel, Alexander; Saih, Youssef; Gimenez, Michel; Pelletier, Jeremie; Kü hn, Fritz Elmar; D´ Elia, Valerio; Basset, Jean-Marie

2016-01-01

Robust and selective catalytic systems based on early transition metal halides (Y, Sc, Zr) and organic nucleophiles were found able to quantitatively capture CO2 from diluted streams via formation of hemicarbonate species and to convert it to cyclic organic carbonates under ambient conditions. This observation was exploited in the direct and selective chemical fixation of flue gas CO2 collected from an industrial exhaust, affording high degrees of CO2 capture and conversion.

Highly integrated CO2 capture and conversion: Direct synthesis of cyclic carbonates from industrial flue gas

KAUST Repository

Barthel, Alexander

2016-02-08

Robust and selective catalytic systems based on early transition metal halides (Y, Sc, Zr) and organic nucleophiles were found able to quantitatively capture CO2 from diluted streams via formation of hemicarbonate species and to convert it to cyclic organic carbonates under ambient conditions. This observation was exploited in the direct and selective chemical fixation of flue gas CO2 collected from an industrial exhaust, affording high degrees of CO2 capture and conversion.

Geological Storage of CO2. Site Selection Criteria

International Nuclear Information System (INIS)

Ruiz, C.; Martinez, R.; Recreo, F.; Prado, P.; Campos, R.; Pelayo, M.; Losa, A. de la; Hurtado, A.; Lomba, L.; Perez del Villar, L.; Ortiz, G.; Sastre, J.; Zapatero, M. A.; Suarez, I.; Arenillas, A.

2007-01-01

In year 2002 the Spanish Parliament unanimously passed the ratification of the Kyoto Protocol, signed December 1997, compromising to limiting the greenhouse gas emissions increase. Later on, the Environment Ministry submitted the Spanish National Assignment Emissions Plan to the European Union and in year 2005 the Spanish Greenhouse Gas market started working, establishing taxes to pay in case of exceeding the assigned emissions limits. So, the avoided emissions of CO2 have now an economic value that is promoting new anthropogenic CO2 emissions reduction technologies. Carbon Capture and Storage (CCS) are among these new technological developments for mitigating or eliminate climate change. CO2 can be stored in geological formations such as depleted oil or gas fields, deep permeable saline water saturated formations and unmailable coal seams, among others. This report seeks to establish the selection criteria for suitable geological formations for CO2 storage in the Spanish national territory, paying attention to both the operational and performance requirements of these storage systems. The report presents the physical and chemical properties and performance of CO2 under storage conditions, the transport and reaction processes of both supercritical and gaseous CO2, and CO2 trapping mechanisms in geological formations. The main part of the report is devoted to geological criteria at watershed, site and formation scales. (Author) 100 refs

Geological Storage of CO2. Site Selection Criteria

International Nuclear Information System (INIS)

Ruiz, C.; Martinez, R.; Recreo, F.; Prado, P.; Campos, R.; Pelayo, M.; Losa, A. de la; Hurtado, A.; Lomba, L.; Perez del Villar, L.; Ortiz, G.; Sastre, J.

2006-01-01

In year 2002 the Spanish Parliament unanimously passed the ratification of the Kyoto Protocol, signed December 1997, compromising to limiting the greenhouse gas emissions increase. Later on, the Environment Ministry submitted the Spanish National Assignment Emissions Plan to the European Union and in year 2005 the Spanish Greenhouse Gas market started working, establishing taxes to pay in case of exceeding the assigned emissions limits. So, the avoided emissions of CO2 have now an economic value that is promoting new anthropogenic CO2 emissions reduction technologies. Carbon Capture and Storage (CCS) are among these new technological developments for mitigating or eliminate climate change. CO2 can be stored in geological formations such as depleted oil or gas fields, deep permeable saline water saturated formations and unmineable coal seams, among others. This report seeks to establish the selection criteria for suitable geological formations for CO2 storage in the Spanish national territory, paying attention to both the operational and performance requirements of these storage systems. The report presents the physical and chemical properties and performance of CO2 under storage conditions, the transport and reaction processes of both supercritical and gaseous CO2, and CO2 trapping mechanisms in geological formations. The main part of the report is devoted to geological criteria at watershed, site and formation scales. (Author) 100 ref

The European Carbon dioxide Capture and Storage Laboratory Infrastructure (ECCSEL

Directory of Open Access Journals (Sweden)

Sverre Quale

2016-10-01

Full Text Available The transition to a non-emitting energy mix for power generation will take decades. This transition will need to be sustainable, e.g. economically affordable. Fossil fuels which are abundant have an important role to play in this respect, provided that Carbon Capture and Storage (CCS is progressively implemented. CCS is the only way to reduce emissions from energy intensive industries.Thus, the need for upgraded and new CCS research facilities is widely recognised among stakeholders across Europe, as emphasised by the Zero Emissions Platform (ZEP [1] and the European Energy Research Alliance on CCS (EERA-CCS [2].The European Carbon Dioxide Capture and Storage Laboratory Infrastructure, ECCSEL, provides funders, operators and researchers with significant benefits by offering access to world-class research facilities that, in many cases, are unlikely for a single nation to support in isolation. This implies creation of synergy and the avoidance of duplication as well as streamlining of funding for research facilities.ECCSEL offers open access to its advanced laboratories for talented scientists and visiting researchers to conduct cutting-edge research.In the planning of ECCSEL, gap analyses were performed and CCS technologies have been reviewed to underpin and envisage the future experimental setup; 1 Making use of readily available facilities, 2 Modifying existing facilities, and 3 Planning and building entirely new advanced facilities.The investments required for the first ten years (2015–2025 are expected to be in the range of €80–120 million. These investments show the current level of ambition, as proposed during the preparatory phase (2011–2014.Entering the implementation phase in 2015, 9 European countries signed Letter of Intent (LoI to join a ECCSEL legal entity: France, United Kingdom, Netherlands, Italy, Spain, Poland, Greece, Norway and Switzerland (active observer. As the EU ERIC-regulation [3] would offer the most

Influence of high-temperature steam on the reactivity of CaO sorbent for CO₂ capture.

Science.gov (United States)

Donat, Felix; Florin, Nicholas H; Anthony, Edward J; Fennell, Paul S

2012-01-17

Calcium looping is a high-temperature CO(2) capture technology applicable to the postcombustion capture of CO(2) from power station flue gas, or integrated with fuel conversion in precombustion CO(2) capture schemes. The capture technology uses solid CaO sorbent derived from natural limestone and takes advantage of the reversible reaction between CaO and CO(2) to form CaCO(3); that is, to achieve the separation of CO(2) from flue or fuel gas, and produce a pure stream of CO(2) suitable for geological storage. An important characteristic of the sorbent, affecting the cost-efficiency of this technology, is the decay in reactivity of the sorbent over multiple CO(2) capture-and-release cycles. This work reports on the influence of high-temperature steam, which will be present in flue (about 5-10%) and fuel (∼20%) gases, on the reactivity of CaO sorbent derived from four natural limestones. A significant increase in the reactivity of these sorbents was found for 30 cycles in the presence of steam (from 1-20%). Steam influences the sorbent reactivity in two ways. Steam present during calcination promotes sintering that produces a sorbent morphology with most of the pore volume associated with larger pores of ∼50 nm in diameter, and which appears to be relatively more stable than the pore structure that evolves when no steam is present. The presence of steam during carbonation reduces the diffusion resistance during carbonation. We observed a synergistic effect, i.e., the highest reactivity was observed when steam was present for both calcination and carbonation.

Thermophysical Properties and Phase Behavior of Fluids for Application in Carbon Capture and Storage Processes.

Science.gov (United States)

Trusler, J P Martin

2017-06-07

Phase behavior and thermophysical properties of mixtures of carbon dioxide with various other substances are very important for the design and operation of carbon capture and storage (CCS) processes. The available empirical data are reviewed, together with some models for the calculation of these properties. The systems considered in detail are, first, mixtures of carbon dioxide, water, and salts; second, carbon dioxide-rich nonelectrolyte mixtures; and third, mixtures of carbon dioxide with water and amines. The empirical data and the plethora of available models permit the estimation of key fluid properties required in the design and operation of CCS processes. The engineering community would benefit from the further development, and delivery in convenient form, of a small number of these models sufficient to encompass the component slate and operating conditions of CCS processes.

Facile Synthesis of Magnetic Mesoporous Hollow Carbon Microspheres for Rapid Capture of Low-Concentration Peptides

OpenAIRE

Cheng, Gong; Zhou, Ming-Da; Zheng, Si-Yang

2014-01-01

Mesoporous and hollow carbon microspheres embedded with magnetic nanoparticles (denoted as MHM) were prepared via a facile self-sacrificial method for rapid capture of low-abundant peptides from complex biological samples. The morphology, structure, surface property, and magnetism were well-characterized. The hollow magnetic carbon microspheres have a saturation magnetization value of 130.2 emu g?1 at room temperature and a Brunauer?Emmett?Teller specific surface area of 48.8 m2 g?1 with an a...

Prospective techno-economic and environmental assessment of carbon capture at a refinery and CO

NARCIS (Netherlands)

Fernandez Dacosta, C.; Van Der Spek, Mijndert; Hung, Christine Roxanne; Oregionni, Gabriel David; Skagestad, Ragnhild; Parihar, Prashant; Gokak, D. T.; Strømman, Anders Hammer; Ramirez Ramirez, C.A.

2017-01-01

CO₂ utilisation is gaining interest as a potential element towards a sustainable economy. CO₂ can be used as feedstock in the synthesis of fuels, chemicals and polymers. This study presents a prospective assessment of carbon capture from a hydrogen unit at a refinery, where

CO2 Capture by Absorption with Potassium Carbonate

Energy Technology Data Exchange (ETDEWEB)

Gary T. Rochelle; Eric Chen; Babatunde Oyenekan; Andrew Sexton; Jason Davis; Marcus Hilliard; Amorvadee Veawab

2006-07-28

The objective of this work is to improve the process for CO{sub 2} capture by alkanolamine absorption/stripping by developing an alternative solvent, aqueous K{sub 2}CO{sub 3} promoted by piperazine. The pilot plant data have been reconciled using 17% inlet CO{sub 2}. A rate-based model demonstrates that the stripper is primarily controlled by liquid film mast transfer resistance, with kinetics at vacuum and diffusion of reactants and products at normal pressure. An additional major unknown ion, probably glyoxylate, has been observed in MEA degradation. Precipitation of gypsum may be a feasible approach to removing sulphate from amine solutions and providing for simultaneous removal of CO{sub 2} and SO{sub 2}. Corrosion of carbon steel in uninhibited MEA solution is increased by increased amine concentration, by addition of piperazine, and by greater CO{sub 2} loading.

Electrochemical and corrosion properties of carbon steel in simulated geological disposal environments

International Nuclear Information System (INIS)

Sugimoto, Katsuhisa

2011-01-01

This paper reviews electrochemical and corrosion studies on the application of carbon steel to an overpack container, which is used for the geological disposal of radioactive wastes. Deaerated alkaline Na 2 SO 4 -NaHCO 3 - NaCl solutions and bentonite soaked with the solutions are used as simulated geological disposal environments. Electrochemical studies show the corrosion of the steel in an early stage is the activation control. Corrosion rates are controlled by the composition of the solutions, alloying elements, and the structure of the steel. The rates decrease with time due to the formation of FeCO 3 (siderite) film on the steel. Immersion corrosion tests show general corrosion morphology. Average corrosion rates of long duration have been evaluated. Clear proofs of the initiation of localized corrosion, such as pitting, crevice corrosion, hydrogen embrittlement and stress-corrosion cracking, have not been reported. (author)

Preparation and Characterization of Impregnated Commercial Rice Husks Activated Carbon with Piperazine for Carbon Dioxide (CO2) Capture

Science.gov (United States)

Masoum Raman, S. N.; Ismail, N. A.; Jamari, S. S.

2017-06-01

Development of effective materials for carbon dioxide (CO2) capture technology is a fundamental importance to reduce CO2 emissions. This work establishes the addition of amine functional group on the surface of activated carbon to further improve the adsorption capacity of CO2. Rice husks activated carbon were modified using wet impregnation method by introducing piperazine onto the activated carbon surfaces at different concentrations and mixture ratios. These modified activated carbons were characterized by using X-Ray Diffraction (XRD), Brunauer, Emmett and Teller (BET), Fourier Transform Infrared Spectroscopy (FTIR) and Field Emission Scanning Electron Microscopy (FESEM). The results from XRD analysis show the presence of polyethylene butane at diffraction angles of 21.8° and 36.2° for modified activated carbon with increasing intensity corresponding to increase in piperazine concentration. BET results found the surface area and pore volume of non-impregnated activated carbon to be 126.69 m2/g and 0.081 cm3/g respectively, while the modified activated carbons with 4M of piperazine have lower surface area and pore volume which is 6.77 m2/g and 0.015 cm3/g respectively. At 10M concentration, the surface area and pore volume are the lowest which is 4.48 m2/g and 0.0065 cm3/g respectively. These results indicate the piperazine being filled inside the activated carbon pores thus, lowering the surface area and pore volume of the activated carbon. From the FTIR analysis, the presence of peaks at 3312 cm-1 and 1636 cm-1 proved the existence of reaction between carboxyl groups on the activated carbon surfaces with piperazine. The surface morphology of activated carbon can be clearly seen through FESEM analysis. The modified activated carbon contains fewer pores than non-modified activated carbon as the pores have been covered with piperazine.

Ultraviolet modification of Chlamydomonas reinhardtii for carbon capture

Directory of Open Access Journals (Sweden)

Gopal NS

2016-04-01

Full Text Available Nikhil S Gopal,1 K Sudhakar2 1The Lawrenceville School, Lawrenceville, NJ, USA; 2Bioenergy Laboratory, Malauna Azad National Institute of Technology, Bhopal, India Purpose: Carbon dioxide (CO2 levels have been rising rapidly. Algae are single-cell organisms with highly efficient CO2 uptake mechanisms. Algae yield two to ten times more biomass versus terrestrial plants and can grow nearly anywhere. Large scale CO2 sequestration is not yet sustainable due to high amounts of nitrogen (N and phosphate (P needed to grow algae in media. Methods: Mutant strains of Chlamydomonas reinhardtii were created using ultraviolet light (2.2–3 K J/m2 and natural selection using media with 20%–80% lower N and P compared to standard Sueoka's high salt medium. Strains were selected based upon growth in media concentrations varying from 20% to 80% less N/P compared to control. Biomass was compared to wild-type control (CC-125 using direct counts, optical density dry weight, and mean doubling time. Results: Mean doubling time was 20 and 25 hours in the low N and N/P strains, respectively (vs 66 hours in control. Using direct counts, growth rates of mutant strains of low N and N/P cultures were not statistically different from control (P=0.37 and 0.70, respectively. Conclusion: Two new strains of algae, as well as wild-type control, were able to grow while using 20%–40% less N and P. Ultraviolet light-based modification of algae is an inexpensive and alternative option to genetic engineering techniques. This technique might make larger scale biosequestration possible. Keywords: biosequestration, ultraviolet, carbon sequestration, carbon capture, algae

Investigating the Fundamental Scientific Issues Affecting the Long-term Geologic Storage of Carbon Dioxide

Energy Technology Data Exchange (ETDEWEB)

Spangler, Lee [Montana State Univ., Bozeman, MT (United States); Cunningham, Alfred [Montana State Univ., Bozeman, MT (United States); Barnhart, Elliot [Montana State Univ., Bozeman, MT (United States); Lageson, David [Montana State Univ., Bozeman, MT (United States); Nall, Anita [Montana State Univ., Bozeman, MT (United States); Dobeck, Laura [Montana State Univ., Bozeman, MT (United States); Repasky, Kevin [Montana State Univ., Bozeman, MT (United States); Shaw, Joseph [Montana State Univ., Bozeman, MT (United States); Nugent, Paul [Montana State Univ., Bozeman, MT (United States); Johnson, Jennifer [Montana State Univ., Bozeman, MT (United States); Hogan, Justin [Montana State Univ., Bozeman, MT (United States); Codd, Sarah [Montana State Univ., Bozeman, MT (United States); Bray, Joshua [Montana State Univ., Bozeman, MT (United States); Prather, Cody [Montana State Univ., Bozeman, MT (United States); McGrail, B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Oldenburg, Curtis [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Wagoner, Jeff [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Pawar, Rajesh [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2014-12-19

The Zero Emissions Research and Technology (ZERT) collaborative was formed to address basic science and engineering knowledge gaps relevant to geologic carbon sequestration. The original funding round of ZERT (ZERT I) identified and addressed many of these gaps. ZERT II has focused on specific science and technology areas identified in ZERT I that showed strong promise and needed greater effort to fully develop.

Evaluation of Ankistrodesmus falcatus for Bicarbonate-Based Integrated Carbon Capture System (BICCAPS

Directory of Open Access Journals (Sweden)

Beltran Arnel B.

2018-01-01

Full Text Available This study evaluates the performance of alkaliphilic microalgae Ankistrodesmus falcatus in the Bicarbonate-based Integrated Carbon Capture and Algae Production System (BICCAPS. The system utilized bicarbonate as carbon source for microalgae production. BICCAPS parameters such as pH, algal biomass productivity and CO2 utilization (inorganic carbon conversion, Ci were observed at different sodium bicarbonate (NaHCO3 loading concentration and type of culture media. The highest productivity was observed at 10 g/L of NaHCO3 loading in BRSP medium at 3.5539 mg/L/day. This value is 30% lower compared to the control experiment (continuously aerated bioreactor. The Ci values of the different system ranges from 1.17 x 10-4 to 1.51 x 10-4 moles/L/day. Both the pH of the BRSP and NPK media at 10 g/L and 30g/L loading of NaHCO3 increased through time. The result shows that A. falcatus has a potential in BICCAPS utilization.

The National Carbon Capture Center at the Power Systems Development Facility: Topical Report

Energy Technology Data Exchange (ETDEWEB)

None, None

2011-03-01

The Power Systems Development Facility (PSDF) is a state-of-the-art test center sponsored by the U.S. Department of Energy and dedicated to the advancement of clean coal technology. In addition to the development of advanced coal gasification processes, the PSDF features the National Carbon Capture Center (NCCC) to study CO2 capture from coal-derived syngas and flue gas. The newly established NCCC will include multiple, adaptable test skids that will allow technology development of CO2 capture concepts using coal-derived syngas and flue gas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity. During the Budget Period One reporting period, efforts at the PSDF/NCCC focused on developing a screening process for testing consideration of new technologies; designing and constructing pre- and post-combustion CO2 capture facilities; developing sampling and analytical methods; expanding fuel flexibility of the Transport Gasification process; and operating the gasification process for technology research and for syngas generation to test syngas conditioning technologies.

Technology roadmap study on carbon capture, utilization and storage in China

International Nuclear Information System (INIS)

Zhang, Xian; Fan, Jing-Li; Wei, Yi-Ming

2013-01-01

Carbon capture, utilization and storage (CCUS) technology will likely become an important approach to reduce carbon dioxide (CO 2 ) emissions and optimize the structure of energy consumption in China in the future. In order to provide guidance and recommendations for CCUS Research, Development and Demonstration in China, a high level stakeholder workshop was held in Chongqing in June 2011 to develop a technology roadmap for the development of CCUS technology. This roadmap outlines the overall vision to provide technically viable and economically affordable technological options to combat climate change and facilitate socio-economic development in China. Based on this vision, milestone goals from 2010 to 2030 are set out in accordance with the technology development environment and current status in China. This study identifies the critical technologies in capture, transport, utilization and storage of CO 2 and proposes technical priorities in the different stages of each technical aspect by evaluating indices such as the objective contribution rate and technical maturity, and gives recommendations on deployment of full-chain CCUS demonstration projects. Policies which would support CCUS are also suggested in this study. - Highlights: • A technology roadmap for CCUS development in China from 2010 to 2030 is presented. • Sound data and analysis in combination with expert workshops are used. • Critical technologies in CCUS are identified. • Priority actions of all stages are identified and proposed. • Guidance and recommendations for CCUS RD and D are provided

Probabilistic Assessment of Above Zone Pressure Predictions at a Geologic Carbon Storage Site

Energy Technology Data Exchange (ETDEWEB)

Namhata, Argha; Oladyshkin, Sergey; Dilmore, Robert M.; Zhang, Liwei; Nakles, David V.

2016-12-01

Carbon dioxide (CO2) storage into geological formations is regarded as an important mitigation strategy for anthropogenic CO2 emissions to the atmosphere. This study first simulates the leakage of CO2 and brine from a storage reservoir through the caprock. Then, we estimate the resulting pressure changes at the zone overlying the caprock also known as Above Zone Monitoring Interval (AZMI). A data-driven approach of arbitrary Polynomial Chaos (aPC) Expansion is then used to quantify the uncertainty in the above zone pressure prediction based on the uncertainties in different geologic parameters. Finally, a global sensitivity analysis is performed with Sobol indices based on the aPC technique to determine the relative importance of different parameters on pressure prediction. The results indicate that there can be uncertainty in pressure prediction locally around the leakage zones. The degree of such uncertainty in prediction depends on the quality of site specific information available for analysis. The scientific results from this study provide substantial insight that there is a need for site-specific data for efficient predictions of risks associated with storage activities. The presented approach can provide a basis of optimized pressure based monitoring network design at carbon storage sites.

Sourcing of Steam and Electricity for Carbon Capture Retrofits.

Science.gov (United States)

Supekar, Sarang D; Skerlos, Steven J

2017-11-07

This paper compares different steam and electricity sources for carbon capture and sequestration (CCS) retrofits of pulverized coal (PC) and natural gas combined cycle (NGCC) power plants. Analytical expressions for the thermal efficiency of these power plants are derived under 16 different CCS retrofit scenarios for the purpose of illustrating their environmental and economic characteristics. The scenarios emerge from combinations of steam and electricity sources, fuel used in each source, steam generation equipment and process details, and the extent of CO 2 capture. Comparing these scenarios reveals distinct trade-offs between thermal efficiency, net power output, levelized cost, profit, and net CO 2 reduction. Despite causing the highest loss in useful power output, bleeding steam and extracting electric power from the main power plant to meet the CCS plant's electricity and steam demand maximizes plant efficiency and profit while minimizing emissions and levelized cost when wholesale electricity prices are below 4.5 and 5.2 US¢/kWh for PC-CCS and NGCC-CCS plants, respectively. At prices higher than these higher profits for operating CCS retrofits can be obtained by meeting 100% of the CCS plant's electric power demand using an auxiliary natural gas turbine-based combined heat and power plant.

Algal capture of carbon dioxide; biomass generation as a tool for greenhouse gas mitigation with reference to New Zealand energy strategy and policy

International Nuclear Information System (INIS)

Packer, Mike

2009-01-01

The use of algae to capture carbon dioxide as a method for greenhouse gas mitigation is discussed. A small fraction of the sunlight energy that bathes Earth is captured by photosynthesis and drives most living systems. Life on Earth is carbon-based and the energy is used to fix atmospheric carbon dioxide into biological material (biomass), indeed fossil fuels that we consume today are a legacy of mostly algal photosynthesis. Algae can be thought of as marine and freshwater plants that have higher photosynthetic efficiencies than terrestrial plants and are more efficient capturing carbon (Box 1). They have other favourable characteristics for this purpose. In the context of New Zealand energy strategy and policy I discuss progress in growing algae and seaweeds with emphasis on their application for exhaust flue carbon recycling for possible generation of useful biomass. I also introduce schemes utilising wild oceanic algae for carbon dioxide sequestration and the merits and possible adverse effects of using this approach. This paper is designed as an approachable review of the science and technology for policy makers and a summary of the New Zealand policy environment for those wishing to deploy biological carbon sequestration.

Superior capture of CO2 achieved by introducing extra-framework cations into N-doped microporous carbon

KAUST Repository

Zhao, Yunfeng; Liu, Xin; Yao, Kexin; Zhao, Lan; Han, Yu

2012-01-01

We designed and prepared a novel microporous carbon material (KNC-A-K) for selective CO2 capture. The combination of a high N-doping concentration (>10 wt %) and extra-framework cations, which were introduced into carbonaceous sorbents

The precise self-assembly of individual carbon nanotubes using magnetic capturing and fluidic alignment

Energy Technology Data Exchange (ETDEWEB)

Shim, Joon S; Rust, Michael J; Do, Jaephil; Ahn, Chong H [Department of Electrical and Computer Engineering, Microsystems and BioMEMS Laboratory, University of Cincinnati, Cincinnati, OH 45221 (United States); Yun, Yeo-Heung; Schulz, Mark J [Department of Mechanical Engineering, University of Cincinnati, 45221 (United States); Shanov, Vesselin, E-mail: chong.ahn@uc.ed [Department of Chemical and Materials Engineering, University of Cincinnati, 45221 (United States)

2009-08-12

A new method for the self-assembly of a carbon nanotube (CNT) using magnetic capturing and fluidic alignment has been developed and characterized in this work. In this new method, the residual iron (Fe) catalyst positioned at one end of the CNT was utilized as a self-assembly driver to attract and position the CNT, while the assembled CNT was aligned by the shear force induced from the fluid flow through the assembly channel. The self-assembly procedures were successfully developed and the electrical properties of the assembled multi-walled carbon nanotube (MWNT) and single-walled carbon nanotube (SWNT) were fully characterized. The new assembly method developed in this work shows its feasibility for the precise self-assembly of parallel CNTs for electronic devices and nanobiosensors.

Pilot Studies of Geologic and Terrestrial Carbon Sequestration in the Big Sky Region, USA, and Opportunities for Commercial Scale Deployment of New Technologies

Science.gov (United States)

Waggoner, L. A.; Capalbo, S. M.; Talbott, J.

2007-05-01

Within the Big Sky region, including Montana, Idaho, South Dakota, Wyoming and the Pacific Northwest, industry is developing new coal-fired power plants using the abundant coal and other fossil-based resources. Of crucial importance to future development programs are robust carbon mitigation plans that include a technical and economic assessment of regional carbon sequestration opportunities. The objective of the Big Sky Carbon Sequestration Partnership (BSCSP) is to promote the development of a regional framework and infrastructure required to validate and deploy carbon sequestration technologies. Initial work compiled sources and potential sinks for carbon dioxide (CO2) in the Big Sky Region and developed the online Carbon Atlas. Current efforts couple geologic and terrestrial field validation tests with market assessments, economic analysis and regulatory and public outreach. The primary geological efforts are in the demonstration of carbon storage in mafic/basalt formations, a geology not yet well characterized but with significant long-term storage potential in the region and other parts of the world; and in the Madison Formation, a large carbonate aquifer in Wyoming and Montana. Terrestrial sequestration relies on management practices and technologies to remove atmospheric CO2 to storage in trees, plants, and soil. This indirect sequestration method can be implemented today and is on the front-line of voluntary, market-based approaches to reduce CO2 emissions. Details of pilot projects are presented including: new technologies, challenges and successes of projects and potential for commercial-scale deployment.

The thiocyanate anion is a primary driver of carbon dioxide capture by ionic liquids

Science.gov (United States)

Chaban, Vitaly

2015-01-01

Carbon dioxide, CO2, capture by room-temperature ionic liquids (RTILs) is a vivid research area featuring both accomplishments and frustrations. This work employs the PM7-MD method to simulate adsorption of CO2 by 1,3-dimethylimidazolium thiocyanate at 300 K. The obtained result evidences that the thiocyanate anion plays a key role in gas capture, whereas the impact of the 1,3-dimethylimidazolium cation is mediocre. Decomposition of the computed wave function on the individual molecular orbitals confirms that CO2-SCN binding extends beyond just expected electrostatic interactions in the ion-molecular system and involves partial sharing of valence orbitals.

Economic and Environmental Assessment of Natural Gas Plants with Carbon Capture and Storage (NGCC-CCS)

Science.gov (United States)

The CO2 intensity of electricity produced by state-of-the-art natural gas combined-cycle turbines (NGCC) isapproximately one-third that of the U.S. fleet of existing coal plants. Compared to new nuclear plants and coal plantswith integrated carbon capture, NGCC has a lower invest...

Enzymes in CO2 Capture

DEFF Research Database (Denmark)

Fosbøl, Philip Loldrup; Gladis, Arne; Thomsen, Kaj

The enzyme Carbonic Anhydrase (CA) can accelerate the absorption rate of CO2 into aqueous solutions by several-fold. It exist in almost all living organisms and catalyses different important processes like CO2 transport, respiration and the acid-base balances. A new technology in the field...... of carbon capture is the application of enzymes for acceleration of typically slow ternary amines or inorganic carbonates. There is a hidden potential to revive currently infeasible amines which have an interesting low energy consumption for regeneration but too slow kinetics for viable CO2 capture. The aim...... of this work is to discuss the measurements of kinetic properties for CA promoted CO2 capture solvent systems. The development of a rate-based model for enzymes will be discussed showing the principles of implementation and the results on using a well-known ternary amine for CO2 capture. Conclusions...

Development of Specific Rules for the Application of Life Cycle Assessment to Carbon Capture and Storage

Directory of Open Access Journals (Sweden)

Michela Gallo

2013-03-01

Full Text Available Carbon Capture and Storage (CCS is a very innovative and promising solution for greenhouse gases (GHG reduction, i.e., capturing carbon dioxide (CO2 at its source and storing it indefinitely to avoid its release to the atmosphere. This paper investigates a set of key issues in the development of specific rules for the application of Life Cycle Assessment (LCA to CCS. The following LCA-based information are addressed in this work: definition of service type, definition of functional unit, definition of system boundaries, choice of allocation rules, choice of selected Life Cycle Inventory (LCI results or other selected parameters for description of environmental performance. From a communication perspective, the specific rules defined in this study have been developed coherently with the requirements of a type III environment label scheme, the International EPD® System, according to the ISO 14025 standard.

Irreversible Change of the Pore Structure of ZIF-8 in Carbon Dioxide Capture with Water Coexistence

DEFF Research Database (Denmark)

Liu, Huang; Guo, Ping; Regueira Muñiz, Teresa

2016-01-01

The performance of zeolitic imidazolate framework 8 (ZIF-8) for CO2 capture under three different conditions (wetted ZIF-8, ZIF-8/water slurry, and ZIF-8/water-glycol slurry) was systemically investigated. This investigation included the study of the pore structure stability of ZIF-8 by using X......-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and Raman detection technologies. Our results show that the CO2 adsorption ability of ZIF-8 could be substantially increased under the existence of liquid water. However, the structure characterization of the recovered ZIF-8...... showed an irreversible change of its framework, which occurs during the CO2 capture process. It was found that there is an irreversible chemical reaction among ZIF-8, water, and CO2, which creates both zinc carbonate (or zinc carbonate hydroxides) and single 2-methylimidazole crystals, and therefore...

A Lithology Based Map Unit Schema For Onegeology Regional Geologic Map Integration

Science.gov (United States)

Moosdorf, N.; Richard, S. M.

2012-12-01

A system of lithogenetic categories for a global lithological map (GLiM, http://www.ifbm.zmaw.de/index.php?id=6460&L=3) has been compiled based on analysis of lithology/genesis categories for regional geologic maps for the entire globe. The scheme is presented for discussion and comment. Analysis of units on a variety of regional geologic maps indicates that units are defined based on assemblages of rock types, as well as their genetic type. In this compilation of continental geology, outcropping surface materials are dominantly sediment/sedimentary rock; major subdivisions of the sedimentary category include clastic sediment, carbonate sedimentary rocks, clastic sedimentary rocks, mixed carbonate and clastic sedimentary rock, colluvium and residuum. Significant areas of mixed igneous and metamorphic rock are also present. A system of global categories to characterize the lithology of regional geologic units is important for Earth System models of matter fluxes to soils, ecosystems, rivers and oceans, and for regional analysis of Earth surface processes at global scale. Because different applications of the classification scheme will focus on different lithologic constituents in mixed units, an ontology-type representation of the scheme that assigns properties to the units in an analyzable manner will be pursued. The OneGeology project is promoting deployment of geologic map services at million scale for all nations. Although initial efforts are commonly simple scanned map WMS services, the intention is to move towards data-based map services that categorize map units with standard vocabularies to allow use of a common map legend for better visual integration of the maps (e.g. see OneGeology Europe, http://onegeology-europe.brgm.fr/ geoportal/ viewer.jsp). Current categorization of regional units with a single lithology from the CGI SimpleLithology (http://resource.geosciml.org/201202/ Vocab2012html/ SimpleLithology201012.html) vocabulary poorly captures the

Carbon Dioxide Capture from Flue Gas : Development and Evaluation of Existing and Novel Process Concepts

NARCIS (Netherlands)

Abu Zahra, M.R.M.

2009-01-01

One of the main global challenges in the years to come is to reduce the CO2 emissions in view of the apparent contribution to global warming. Carbon dioxide capture, transport, and storage (CCS) from fossil fuel fired power plants is drawing increased interest as an intermediate solution towards

The Environmental and Economic Sustainability of Carbon Capture and Storage

Directory of Open Access Journals (Sweden)

Mayuran Sivapalan

2011-05-01

Full Text Available For carbon capture and storage (CCS to be a truly effective option in our efforts to mitigate climate change, it must be sustainable. That means that CCS must deliver consistent environmental and social benefits which exceed its costs of capital, energy and operation; it must be protective of the environment and human health over the long term; and it must be suitable for deployment on a significant scale. CCS is one of the more expensive and technically challenging carbon emissions abatement options available, and CCS must first and foremost be considered in the context of the other things that can be done to reduce emissions, as a part of an overall optimally efficient, sustainable and economic mitigation plan. This elevates the analysis beyond a simple comparison of the cost per tonne of CO2 abated—there are inherent tradeoffs with a range of other factors (such as water, NOx, SOx, biodiversity, energy, and human health and safety, among others which must also be considered if we are to achieve truly sustainable mitigation. The full life-cycle cost of CCS must be considered in the context of the overall social, environmental and economic benefits which it creates, and the costs associated with environmental and social risks it presents. Such analysis reveals that all CCS is not created equal. There is a wide range of technological options available which can be used in a variety of industries and applications—indeed CCS is not applicable to every industry. Stationary fossil-fuel powered energy and large scale petroleum industry operations are two examples of industries which could benefit from CCS. Capturing and geo-sequestering CO2 entrained in natural gas can be economic and sustainable at relatively low carbon prices, and in many jurisdictions makes financial sense for operators to deploy now, if suitable secure disposal reservoirs are available close by. Retrofitting existing coal-fired power plants, however, is more expensive and

The environmental and economic sustainability of carbon capture and storage.

Science.gov (United States)

Hardisty, Paul E; Sivapalan, Mayuran; Brooks, Peter

2011-05-01

For carbon capture and storage (CCS) to be a truly effective option in our efforts to mitigate climate change, it must be sustainable. That means that CCS must deliver consistent environmental and social benefits which exceed its costs of capital, energy and operation; it must be protective of the environment and human health over the long term; and it must be suitable for deployment on a significant scale. CCS is one of the more expensive and technically challenging carbon emissions abatement options available, and CCS must first and foremost be considered in the context of the other things that can be done to reduce emissions, as a part of an overall optimally efficient, sustainable and economic mitigation plan. This elevates the analysis beyond a simple comparison of the cost per tonne of CO(2) abated--there are inherent tradeoffs with a range of other factors (such as water, NOx, SOx, biodiversity, energy, and human health and safety, among others) which must also be considered if we are to achieve truly sustainable mitigation. The full life-cycle cost of CCS must be considered in the context of the overall social, environmental and economic benefits which it creates, and the costs associated with environmental and social risks it presents. Such analysis reveals that all CCS is not created equal. There is a wide range of technological options available which can be used in a variety of industries and applications-indeed CCS is not applicable to every industry. Stationary fossil-fuel powered energy and large scale petroleum industry operations are two examples of industries which could benefit from CCS. Capturing and geo-sequestering CO(2) entrained in natural gas can be economic and sustainable at relatively low carbon prices, and in many jurisdictions makes financial sense for operators to deploy now, if suitable secure disposal reservoirs are available close by. Retrofitting existing coal-fired power plants, however, is more expensive and technically

A Step towards Sustainable Society: The Awareness of Carbon Dioxide Emissions, Climate Change and Carbon Capture in Malaysia

OpenAIRE

Ghazali, Zulkipli; Zahid, Muhammad; Kee, Tan Siok; Ibrahim, M. Yussoff

2016-01-01

Public awareness is crucial to mitigate negative impacts on the environment. The aim of the study is to explore the level of public awareness in five states of Malaysia (Perak, Melaka, Johor, Pahang and Terengganu) regarding CO2 emissions, climate change and carbon capture and storage (CCS). A questionnaire floated for exploring public awareness regarding CO2 emissions, climate change and CCS. Based on the questionnaire data was collected from five states (Perak, Melaka, Johor, Pahang and Ter...

Heat and work integration: Fundamental insights and applications to carbon dioxide capture processes

International Nuclear Information System (INIS)

Fu, Chao; Gundersen, Truls

2016-01-01

Highlights: • The problem definition of heat and work integration is introduced. • The fundamental insights of heat and work integration are presented. • The design methodology is illustrated with two small test examples. • Applications of to three carbon dioxide capture processes are presented. - Abstract: The integration of heat has achieved a notable success in the past decades. Pinch Analysis is a well-established methodology for heat integration. Work is an equally important thermodynamic parameter. The enthalpy of a process stream can be changed by the transfer of heat and/or work. Heat and work are actually interchangeable and can thus be integrated. For example, compression processes consume more work at higher temperatures, however, the compression heat may be upgraded and utilized; expansion processes produce more work at higher temperatures, however, more heat may be required. The classical heat integration problem is thus extended to a new research topic about the integration of both heat and work. The aim of this paper is to present the problem definition, fundamental thermodynamic insights and industrial applications of heat and work integration. The results from studies on the three carbon dioxide capture processes show that significant energy savings can be achieved by proper heat and work integration. In the oxy-combustion process, the work consumption for cryogenic air separation is reduced by 10.1%. In the post-combustion membrane separation process, the specific work consumption for carbon dioxide separation is reduced by 12.9%. In the membrane air separation process, the net work consumption (excluding heat consumption) is reduced by 90%.

Combined Pressure, Temperature Contrast and Surface-Enhanced Separation of Carbon Dioxide for Post-Combustion Carbon Capture

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhen [Rice Univ., Houston, TX (United States); Wong, Michael [Rice Univ., Houston, TX (United States); Gupta, Mayank [Rice Univ., Houston, TX (United States); Hirasaki, George [Rice Univ., Houston, TX (United States); Cox, Kenneth [Rice Univ., Houston, TX (United States)

2016-05-01

The Rice University research team developed a hybrid carbon dioxide (CO₂) absorption process combining absorber and stripper columns using a high surface area ceramic foam gas-liquid contactor for enhanced mass transfer and utilizing waste heat for regeneration. This integrated absorber/desorber arrangement will reduce space requirements, an important factor for retrofitting existing coal-fired power plants with CO₂ capture technology. Described in this report, we performed an initial analysis to estimate the technical and economic feasibility of the process. A one-dimensional (1D) CO₂ absorption column was fabricated to measure the hydrodynamic and mass transfer characteristics of the ceramic foam. A bench-scale prototype was constructed to implement the complete CO₂ separation process and tested to study various aspects of fluid flow in the process. A model was developed to simulate the two-dimensional (2D) fluid flow and optimize the CO₂ capture process. Test results were used to develop a final technoeconomic analysis and identify the most appropriate absorbent as well as optimum operating conditions to minimize capital and operating costs. Finally, a technoeconomic study was performed to assess the feasibility of integrating the process into a 600 megawatt electric (MWe) coal-fired power plant. With process optimization, $82/MWh of COE can be achieved using our integrated absorber/desorber CO₂ capture technology, which is very close to DOE's target that no more than a 35% increase in COE with CCS. An environmental, health, and safety (EH&S) assessment of the capture process indicated no significant concern in terms of EH&S effects or legislative compliance.

Can carbon dioxide storage help cut greenhouse emissions? A simplified guide to the IPCC's 'Special Report on Carbon Dioxide Capture and Storage'

International Nuclear Information System (INIS)

2006-06-01

Fossil fuels account for 75 - 80% of today's global energy use and three quarters of humanity's total carbon dioxide emissions. Without specific actions to minimize our impact on the climate, carbon dioxide (CO2) emissions from fossil-fuel energy are projected to swell over the course of the 21st century. The consequences - a global temperature rise of 1.4 - 5.8C and shifting patterns of weather and extreme events - could prove disastrous for future generations. Stabilizing or reducing global emissions of carbon dioxide and other greenhouse gases over the coming decades will challenge human ingenuity. Fortunately, the IPCC's Third Assessment Report, published in 2001, concluded that existing and emerging technologies for limiting emissions could - if supported by the right policies - stabilize atmospheric concentrations of greenhouse gases by the end of the century at levels that would limit further climate change. No single technology will suffice by itself; instead, a combination of technologies will be required. Many of the most promising technologies will contribute by improving the energy efficiency of certain processes and products or by converting solar, wind and other noncarbon power sources into usable energy. But with oil, coal and gas set to remain the primary sources of energy for decades to come, governments and industry are also examining technologies for reducing emissions from these fuels. One such technology is known as carbon dioxide capture and storage. Abbreviated as CCS, this technology could be used by large c1 Introduction stationary 'point sources' such as fossil fuel-fired power plants and industrial facilities to prevent their CO2 emissions from entering the atmosphere and contributing to climate change. To learn more about this technology's potential, the member governments of the United Nations Framework Convention on Climate Change asked the IPCC to assess the current state of knowledge about carbon dioxide storage and capture. The IPCC

Water Vapor Adsorption on Biomass Based Carbons under Post-Combustion CO2 Capture Conditions: Effect of Post-Treatment

Directory of Open Access Journals (Sweden)

Nausika Querejeta

2016-05-01

Full Text Available The effect of post-treatment upon the H2O adsorption performance of biomass-based carbons was studied under post-combustion CO2 capture conditions. Oxygen surface functionalities were partially replaced through heat treatment, acid washing, and wet impregnation with amines. The surface chemistry of the final carbon is strongly affected by the type of post-treatment: acid treatment introduces a greater amount of oxygen whereas it is substantially reduced after thermal treatment. The porous texture of the carbons is also influenced by post-treatment: the wider pore volume is somewhat reduced, while narrow microporosity remains unaltered only after acid treatment. Despite heat treatment leading to a reduction in the number of oxygen surface groups, water vapor adsorption was enhanced in the higher pressure range. On the other hand acid treatment and wet impregnation with amines reduce the total water vapor uptake thus being more suitable for post-combustion CO2 capture applications.

Near-Term Opportunities for Carbon Dioxide Capture and Storage 2007

Energy Technology Data Exchange (ETDEWEB)

NONE

2007-07-01

This document contains the summary report of the workshop on global assessments for near-term opportunities for carbon dioxide capture and storage (CCS), which took place on 21-22 June 2007 in Oslo, Norway. It provided an opportunity for direct dialogue between concerned stakeholders in the global effort to accelerate the development and commercialisation of CCS technology. This is part of a series of three workshops on near-term opportunities for this important mitigation option that will feed into the G8 Plan of Action on Climate Change, Clean Energy and Sustainable Development. The ultimate goal of this effort is to present a report and policy recommendations to the G8 leaders at their 2008 summit meeting in Japan.

A study on the economic feasibility of carbon sequestration with enhanced gas recovery (CSEGR) at Rio Vista, California

OpenAIRE

Zhang, Yingqi; Oldenburg, Curtis M.; Finsterle, Stefan; Bodvarsson, G.S.

2006-01-01

One way to reduce the effects of anthropogenic greenhouse gases on climate is to inject carbon dioxide (CO2) from industrial sources into deep geological formations such as brine formations or depleted oil or gas reservoirs. In this study we develop a system-level model using GoldSim for geological CO2 storage to evaluate performance, economic, and subsequent health, safety and environmental (HSE) issues. The processes considered include CO2 capture and separation, compression, pipeline trans...

Methane production by Methanothermobacter thermautotrophicus to recover energy from carbon dioxide sequestered in geological reservoirs.

Science.gov (United States)

Kawaguchi, Hideo; Sakuma, Takahiro; Nakata, Yuiko; Kobayashi, Hajime; Endo, Keita; Sato, Kozo

2010-07-01

To recover energy from carbon dioxide sequestered in geological reservoirs, the geochemical effects of acidic and substrate- and nutrient-limiting conditions on methane production by the hydrogenotrophic methanogen Methanothermobacter thermautotrophicus were investigated in a simulated deep saline aquifer environment using formation water media retrieved from petroleum reservoirs. 2009 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

The National Carbon Capture Center at the Power Systems Development Facility

Energy Technology Data Exchange (ETDEWEB)

Mosser, Morgan [Southern Company Services, Inc., Wilsonville, AL (United States)

2012-12-31

The Power Systems Development Facility (PSDF) is a state-of-the-art test center sponsored by the U.S. Department of Energy and dedicated to the advancement of clean coal technology. In addition to the development of high efficiency coal gasification processes, the PSDF features the National Carbon Capture Center (NCCC) to promote new technologies for CO₂ capture from coal-derived syngas and flue gas. The NCCC includes multiple, adaptable test skids that allow technology development of CO₂ capture concepts using coal-derived syngas and flue gas in industrial settings. Because of the ability to operate under a wide range of flow rates and process conditions, research at the NCCC can effectively evaluate technologies at various levels of maturity and accelerate their development path to commercialization. During the calendar year 2012 portion of the Budget Period Four reporting period, efforts at the NCCC focused on testing of pre- and post-combustion CO₂ capture processes and gasification support technologies. Preparations for future testing were on-going as well, and involved facility upgrades and collaboration with numerous technology developers. In the area of pre-combustion, testing was conducted on a new water-gas shift catalyst, a CO₂ solvent, and gas separation membranes from four different technology developers, including two membrane systems incorporating major scale-ups. Post-combustion tests involved advanced solvents from three major developers, a gas separation membrane, and two different enzyme technologies. An advanced sensor for gasification operation was evaluated, operation with biomass co-feeding with coal under oxygen-blown conditions was achieved, and progress continued on refining several gasification support technologies.

CFD Simulations of a Regenerative Process for Carbon Dioxide Capture in Advanced Gasification Based Power Systems

Energy Technology Data Exchange (ETDEWEB)

Arastoopour, Hamid [Illinois Inst. of Technology, Chicago, IL (United States); Abbasian, Javad [Illinois Inst. of Technology, Chicago, IL (United States)

2014-07-31

This project describes the work carried out to prepare a highly reactive and mechanically strong MgO based sorbents and to develop a Population Balance Equations (PBE) approach to describe the evolution of the particle porosity distribution that is linked with Computational Fluid Dynamics (CFD) to perform simulations of the CO2 capture and sorbent regeneration. A large number of MgO-based regenerable sorbents were prepared using low cost and abundant dolomite as the base material. Among various preparation parameters investigated the potassium/magnesium (K/Mg) ratio was identified as the key variable affecting the reactivity and CO2 capacity of the sorbent. The optimum K/Mg ratio is about 0.15. The sorbent formulation HD52-P2 was identified as the “best” sorbent formulation and a large batch (one kg) of the sorbent was prepared for the detailed study. The results of parametric study indicate the optimum carbonation and regeneration temperatures are 360° and 500°C, respectively. The results also indicate that steam has a beneficial effect on the rate of carbonation and regeneration of the sorbent and that the reactivity and capacity of the sorbent decreases in the cycling process (sorbent deactivation). The results indicate that to achieve a high CO2 removal efficiency, the bed of sorbent should be operated at a temperature range of 370-410°C which also favors production of hydrogen through the WGS reaction. To describe the carbonation reaction kinetics of the MgO, the Variable Diffusivity shrinking core Model (VDM) was developed in this project, which was shown to accurately fit the experimental data. An important advantage of this model is that the changes in the sorbent conversion with time can be expressed in an explicit manner, which will significantly reduce the CFD computation time. A Computational Fluid Dynamic/Population Balance Equations (CFD/PBE) model was developed that accounts for the particle (sorbent) porosity distribution and a new version of

Life cycle GHG assessment of fossil fuel power plants with carbon capture and storage

International Nuclear Information System (INIS)

Odeh, Naser A.; Cockerill, Timothy T.

2008-01-01

The evaluation of life cycle greenhouse gas emissions from power generation with carbon capture and storage (CCS) is a critical factor in energy and policy analysis. The current paper examines life cycle emissions from three types of fossil-fuel-based power plants, namely supercritical pulverized coal (super-PC), natural gas combined cycle (NGCC) and integrated gasification combined cycle (IGCC), with and without CCS. Results show that, for a 90% CO 2 capture efficiency, life cycle GHG emissions are reduced by 75-84% depending on what technology is used. With GHG emissions less than 170 g/kWh, IGCC technology is found to be favorable to NGCC with CCS. Sensitivity analysis reveals that, for coal power plants, varying the CO 2 capture efficiency and the coal transport distance has a more pronounced effect on life cycle GHG emissions than changing the length of CO 2 transport pipeline. Finally, it is concluded from the current study that while the global warming potential is reduced when MEA-based CO 2 capture is employed, the increase in other air pollutants such as NO x and NH 3 leads to higher eutrophication and acidification potentials

Convenient and large-scale synthesis of nitrogen-rich hierarchical porous carbon spheres for supercapacitors and CO_2 capture

International Nuclear Information System (INIS)

Chang, Binbin; Zhang, Shouren; Yin, Hang; Yang, Baocheng

2017-01-01

Highlights: • Convenient and large-scale synthesis route for N-doped hierarchical porous carbon sphere. • The resultant own spherical morphology, tunable hierarchical porosity, high surface area. • The optimal material exhibits a high CO_2 capture capacity of 4.23 mmol g"−"1. • It shows a large voltage window of 1.8 V for symmetric cell in 0.5 M Na_2SO_4. - Abstract: Herein, considering the great potential of nitrogen-doped hierarchical porous carbons in energy storage and CO_2 capture, we designed a convenient and easily large-scale production strategy for preparing nitrogen-doped hierarchical porous carbon sphere (NHPCS) materials. In this synthesis route, spherical resorcinol-formaldehyde (RF) resins were selected as carbon precursor, and then the ZnCl_2-impregnated RF resin spheres were carbonized in a NH_3 atmosphere at a temperature range of 600–800 °C. During the one-step heat-treatment process, nitrogen atom could be efficiently incorporated into the carbon skeleton, and the interconnected and hierarchical pore structure with different micro/mesopore proportion could be generated and tuned by adjusting the activating agent ZnCl_2 dosage and carbonization temperature. The resultant nitrogen-doped hierarchical porous carbon sphere materials exhibited a satisfactory charge storage capacity, and the optimal sample of NHPCS-2-8 with a high mesopore proportion obtained at 800 °C with a ZnCl_2/RF mass ratio of 2:1 presented a specific capacitance of 273.8 F g"−"1 at a current density of 0.5 A g"−"1. More importantly, the assembled NHPCS-2-8-based symmetric capacitor displayed a high energy density of 17.2 Wh kg"−"1 at a power density of 178.9 W kg"−"1 within a voltage window of 0 ∼ 1.8 V in 0.5 M Na_2SO_4 aqueous electrolyte. In addition, the CO_2 capture application of these NHPCS materials was also explored, and the optimal sample of NHPCS-0-8 with a large micropore proportion prepared at 800 °C exhibited an exceptional CO_2 uptake

Effect of oxygen co-injected with carbon dioxide on Gothic shale caprock–CO₂–brine interaction during geologic carbon sequestration

Energy Technology Data Exchange (ETDEWEB)

Jung, Hun Bok; Um, Wooyong; Cantrell, Kirk J.

2013-09-01

Co-injection of oxygen, a significant component in CO₂ streams produced by the oxyfuel combustion process, can cause a significant alteration of the redox state in deep geologic formations during geologic carbon sequestration. The potential impact of co-injected oxygen on the interaction between synthetic CO₂–brine (0.1 M NaCl) and shale caprock (Gothic shale from the Aneth Unit in Utah) and mobilization of trace metals was investigated at ~ 10 MPa and ~ 75 °C. A range of relative volume percentages of O₂ to CO₂ (0, 1, 4 and 8%) were used in these experiments to address the effect of oxygen on shale–CO₂–brine interaction under various conditions. Major mineral phases in Gothic shale are quartz, calcite, dolomite, montmorillonite, and pyrite. During Gothic shale–CO₂–brine interaction in the presence of oxygen, pyrite oxidation occurred extensively and caused enhanced dissolution of calcite and dolomite. Pyrite oxidation and calcite dissolution subsequently resulted in the precipitation of Fe(III) oxides and gypsum (CaSO₄·2H₂O). In the presence of oxygen, dissolved Mn and Ni were elevated because of oxidative dissolution of pyrite. The mobility of dissolved Ba was controlled by barite (BaSO₄) precipitation in the presence of oxygen. Dissolved U in the experimental brines increased to ~ 8–14 μg/L, with concentrations being slightly higher in the absence of oxygen than in the presence of oxygen. Experimental and modeling results indicate the interaction between shale caprock and oxygen co-injected with CO₂ during geologic carbon sequestration can exert significant impacts on brine pH, solubility of carbonate minerals, stability of sulfide minerals, and mobility of trace metals. The major impact of oxygen is most likely to occur in the zone near CO₂ injection wells where impurity gases can accumulate. Finally, oxygen in CO₂

Southern Adriatic sea as a potential area for CO2 geological storage

International Nuclear Information System (INIS)

Volpi, V.; Forlin, F.; Donda, F.; Civile, D.; Facchin, L.; Sauli, L.; Merson, B.; Sinza-Mendieta, K.; Shams, A.

2015-01-01

The Southern Adriatic Sea is one of the five prospective areas for CO 2 storage being evaluated under the three year (FP7) European SiteChar project dedicated to the characterization of European CO 2 storage sites. The potential reservoir for CO 2 storage is represented by a carbonate formation, the wackstones and packstones of the Scaglia Formation (Upper Cretaceous-Paleogene). In this paper, we present the geological characterization and the 3D modeling that led to the identification of three sites, named Grazia, Rovesti and Grifone, where the Scaglia Formation, with an average thickness of 50 m, reveals good petrophysical characteristics and is overlain by an up to 1 200 thick cap-rock. The vicinity of the selected sites to the Enel - Federico II power plant (one of the major Italian CO 2 emitter) where a pilot plant for CO 2 capture has been already started in April 2010, represents a good opportunity to launch the first Carbon Capture and Storage (CCS) pilot project in Italy and to apply this technology at industrial level, strongly contributing at the same time at reducing the national CO 2 emissions. (authors)

INTEGRATED GEOLOGIC-ENGINEERING MODEL FOR REEF AND CARBONATE SHOAL RESERVOIRS ASSOCIATED WITH PALEOHIGHS: UPPER JURASSIC SMACKOVER FORMATION, NORTHEASTERN GULF OF MEXICO

Energy Technology Data Exchange (ETDEWEB)

Ernest A. Mancini

2003-09-25

The University of Alabama in cooperation with Texas A&M University, McGill University, Longleaf Energy Group, Strago Petroleum Corporation, and Paramount Petroleum Company are undertaking an integrated, interdisciplinary geoscientific and engineering research project. The project is designed to characterize and model reservoir architecture, pore systems and rock-fluid interactions at the pore to field scale in Upper Jurassic Smackover reef and carbonate shoal reservoirs associated with varying degrees of relief on pre-Mesozoic basement paleohighs in the northeastern Gulf of Mexico. The project effort includes the prediction of fluid flow in carbonate reservoirs through reservoir simulation modeling that utilizes geologic reservoir characterization and modeling and the prediction of carbonate reservoir architecture, heterogeneity and quality through seismic imaging. The primary objective of the project is to increase the profitability, producibility and efficiency of recovery of oil from existing and undiscovered Upper Jurassic fields characterized by reef and carbonate shoals associated with pre-Mesozoic basement paleohighs. The principal research effort for Year 3 of the project has been reservoir characterization, 3-D modeling, testing of the geologic-engineering model, and technology transfer. This effort has included six tasks: (1) the study of seismic attributes, (2) petrophysical characterization, (3) data integration, (4) the building of the geologic-engineering model, (5) the testing of the geologic-engineering model and (6) technology transfer. This work was scheduled for completion in Year 3. Progress on the project is as follows: geoscientific reservoir characterization is completed. The architecture, porosity types and heterogeneity of the reef and shoal reservoirs at Appleton and Vocation Fields have been characterized using geological and geophysical data. The study of rock-fluid interactions has been completed. Observations regarding the diagenetic

Carbon Dioxide Capture and Transportation Options in the Illinois Basin

Energy Technology Data Exchange (ETDEWEB)

M. Rostam-Abadi; S. S. Chen; Y. Lu

2004-09-30

This report describes carbon dioxide (CO{sub 2}) capture options from large stationary emission sources in the Illinois Basin, primarily focusing on coal-fired utility power plants. The CO{sub 2} emissions data were collected for utility power plants and industrial facilities over most of Illinois, southwestern Indiana, and western Kentucky. Coal-fired power plants are by far the largest CO{sub 2} emission sources in the Illinois Basin. The data revealed that sources within the Illinois Basin emit about 276 million tonnes of CO2 annually from 122 utility power plants and industrial facilities. Industrial facilities include 48 emission sources and contribute about 10% of total emissions. A process analysis study was conducted to review the suitability of various CO{sub 2} capture technologies for large stationary sources. The advantages and disadvantages of each class of technology were investigated. Based on these analyses, a suitable CO{sub 2} capture technology was assigned to each type of emission source in the Illinois Basin. Techno-economic studies were then conducted to evaluate the energy and economic performances of three coal-based power generation plants with CO{sub 2} capture facilities. The three plants considered were (1) pulverized coal (PC) + post combustion chemical absorption (monoethanolamine, or MEA), (2) integrated gasification combined cycle (IGCC) + pre-combustion physical absorption (Selexol), and (3) oxygen-enriched coal combustion plants. A conventional PC power plant without CO2 capture was also investigated as a baseline plant for comparison. Gross capacities of 266, 533, and 1,054 MW were investigated at each power plant. The economic study considered the burning of both Illinois No. 6 coal and Powder River Basin (PRB) coal. The cost estimation included the cost for compressing the CO{sub 2} stream to pipeline pressure. A process simulation software, CHEMCAD, was employed to perform steady-state simulations of power generation systems

The Biological Deep Sea Hydrothermal Vent as a Model to Study Carbon Dioxide Capturing Enzymes

Directory of Open Access Journals (Sweden)

Premila D. Thongbam

2011-04-01

Full Text Available Deep sea hydrothermal vents are located along the mid-ocean ridge system, near volcanically active areas, where tectonic plates are moving away from each other. Sea water penetrates the fissures of the volcanic bed and is heated by magma. This heated sea water rises to the surface dissolving large amounts of minerals which provide a source of energy and nutrients to chemoautotrophic organisms. Although this environment is characterized by extreme conditions (high temperature, high pressure, chemical toxicity, acidic pH and absence of photosynthesis a diversity of microorganisms and many animal species are specially adapted to this hostile environment. These organisms have developed a very efficient metabolism for the assimilation of inorganic CO2 from the external environment. In order to develop technology for the capture of carbon dioxide to reduce greenhouse gases in the atmosphere, enzymes involved in CO2 fixation and assimilation might be very useful. This review describes some current research concerning CO2 fixation and assimilation in the deep sea environment and possible biotechnological application of enzymes for carbon dioxide capture.

Updated (BP3) Technical and Economic Feasibility Study - Electrochemical Membrane for Carbon Dioxide Capture and Power Generation

Energy Technology Data Exchange (ETDEWEB)

Ghezel-Ayagh, Hossein

2016-10-12

This topical report summarizes the results of an updated Technical & Economic Feasibility Study (T&EFS) which was conducted in Budget Period 3 of the project to evaluate the performance and cost of the Electrochemical Membrane (ECM)-based CO2 capture system. The ECM technology is derived from commercially available inorganic membranes; the same used in FuelCell Energy’s commercial fuel cell power plants and sold under the trade name Direct FuelCell® (DFC®). The ECM stacks are utilized in the Combined Electric Power (generation) And Carbon dioxide Separation (CEPACS) systems which can be deployed as add-ons to conventional power plants (Pulverized Coal, Combined Cycle, etc.) or industrial facilities to simultaneously produce power while capturing >90% of the CO2 from the flue gas. In this study, an ECM-based CEPACS plant was designed to capture and compress >90% of the CO2 (for sequestration or beneficial use) from the flue gas of a reference 550 MW (nominal, net AC) Pulverized Coal (PC) Rankine Cycle (Subcritical steam) power plant. ECM performance was updated based on bench scale ECM stack test results. The system process simulations were performed to generate the CEPACS plant performance estimates. The performance assessment included estimation of the parasitic power consumption for CO2 capture and compression, and the efficiency impact on the PC plant. While the ECM-based CEPACS system for the 550 MW PC plant captures 90% of CO2 from the flue gas, it generates additional (net AC) power after compensating for the auxiliary power requirements of CO2 capture and compression. An equipment list, ECM stacks packaging design, and CEPACS plant layout were developed to facilitate the economic analysis. Vendor quotes were also solicited. The economic feasibility study included estimation of CEPACS plant capital cost, cost of electricity (COE) analyses and estimation of cost per ton of CO2 captured. The incremental COE for the ECM-based CO2 capture is expected to meet

3D Geological Model for "LUSI" - a Deep Geothermal System

Science.gov (United States)

Sohrabi, Reza; Jansen, Gunnar; Mazzini, Adriano; Galvan, Boris; Miller, Stephen A.

2016-04-01

Geothermal applications require the correct simulation of flow and heat transport processes in porous media, and many of these media, like deep volcanic hydrothermal systems, host a certain degree of fracturing. This work aims to understand the heat and fluid transport within a new-born sedimentary hosted geothermal system, termed Lusi, that began erupting in 2006 in East Java, Indonesia. Our goal is to develop conceptual and numerical models capable of simulating multiphase flow within large-scale fractured reservoirs such as the Lusi region, with fractures of arbitrary size, orientation and shape. Additionally, these models can also address a number of other applications, including Enhanced Geothermal Systems (EGS), CO2 sequestration (Carbon Capture and Storage CCS), and nuclear waste isolation. Fractured systems are ubiquitous, with a wide-range of lengths and scales, making difficult the development of a general model that can easily handle this complexity. We are developing a flexible continuum approach with an efficient, accurate numerical simulator based on an appropriate 3D geological model representing the structure of the deep geothermal reservoir. Using previous studies, borehole information and seismic data obtained in the framework of the Lusi Lab project (ERC grant n°308126), we present here the first 3D geological model of Lusi. This model is calculated using implicit 3D potential field or multi-potential fields, depending on the geological context and complexity. This method is based on geological pile containing the geological history of the area and relationship between geological bodies allowing automatic computation of intersections and volume reconstruction. Based on the 3D geological model, we developed a new mesh algorithm to create hexahedral octree meshes to transfer the structural geological information for 3D numerical simulations to quantify Thermal-Hydraulic-Mechanical-Chemical (THMC) physical processes.

U.S. Department of Energy's site screening, site selection, and initial characterization for storage of CO2 in deep geological formations

Science.gov (United States)

Rodosta, T.D.; Litynski, J.T.; Plasynski, S.I.; Hickman, S.; Frailey, S.; Myer, L.

2011-01-01

The U.S. Department of Energy (DOE) is the lead Federal agency for the development and deployment of carbon sequestration technologies. As part of its mission to facilitate technology transfer and develop guidelines from lessons learned, DOE is developing a series of best practice manuals (BPMs) for carbon capture and storage (CCS). The "Site Screening, Site Selection, and Initial Characterization for Storage of CO2 in Deep Geological Formations" BPM is a compilation of best practices and includes flowchart diagrams illustrating the general decision making process for Site Screening, Site Selection, and Initial Characterization. The BPM integrates the knowledge gained from various programmatic efforts, with particular emphasis on the Characterization Phase through pilot-scale CO2 injection testing of the Validation Phase of the Regional Carbon Sequestration Partnership (RCSP) Initiative. Key geologic and surface elements that suitable candidate storage sites should possess are identified, along with example Site Screening, Site Selection, and Initial Characterization protocols for large-scale geologic storage projects located across diverse geologic and regional settings. This manual has been written as a working document, establishing a framework and methodology for proper site selection for CO2 geologic storage. This will be useful for future CO2 emitters, transporters, and storage providers. It will also be of use in informing local, regional, state, and national governmental agencies of best practices in proper sequestration site selection. Furthermore, it will educate the inquisitive general public on options and processes for geologic CO2 storage. In addition to providing best practices, the manual presents a geologic storage resource and capacity classification system. The system provides a "standard" to communicate storage and capacity estimates, uncertainty and project development risk, data guidelines and analyses for adequate site characterization, and

Behavioral responses of Arctica islandica (Bivalvia: Arcticidae) to simulated leakages of carbon dioxide from sub-sea geological storage

International Nuclear Information System (INIS)

Bamber, Shaw D.; Westerlund, Stig

2016-01-01

Highlights: • Valve pumping activity in A. islandica significantly increased at pH 6.2 seawater. • Changes in valve movements were not related to attempted burrowing activities. • Valve activity returned to control levels after 5 days of continuous exposure. • A. islandica tolerate pH reductions likely to follow leakage of sub-sea stored CO_2. - Abstract: Sub-sea geological storage of carbon dioxide (CO_2) provides a viable option for the Carbon Capture and Storage (CCS) approach for reducing atmospheric emissions of this greenhouse gas. Although generally considered to offer a low risk of major leakage, it remains relevant to establish the possible consequences for marine organisms that live in or on sediments overlying these storage areas if such an event may occur. The present study has used a series of laboratory exposures and behavioral bioassays to establish the sensitivity of Arctica islandica to simulated leakages of CO_2. This long-lived bivalve mollusc is widely distributed throughout the North Sea, an area where geological storage is currently taking place and where there are plans to expand this operation significantly. A recently published model has predicted a maximum drop of 1.9 pH units in seawater at the point source of a substantial escape of CO_2 from sub-sea geological storage in this region. Valve movements of A. islandica exposed to reduced pH seawater were recorded continuously using Hall effect proximity sensors. Valve movement regulation is important for optimising the flow of water over the gills, which supplies food and facilitates respiration. A stepwise reduction in seawater pH showed an initial increase in both the rate and extent of valve movements in the majority of individuals tested when pH fell to 6.2 units. Exposing A. islandica to pH 6.2 seawater continuously for seven days resulted in a clear increase in valve movements during the first 40 h of exposure, followed by a gradual reduction in activity intensity over the

Behavioral responses of Arctica islandica (Bivalvia: Arcticidae) to simulated leakages of carbon dioxide from sub-sea geological storage

Energy Technology Data Exchange (ETDEWEB)

Bamber, Shaw D., E-mail: shaw.bamber@iris.no; Westerlund, Stig, E-mail: sw@iris.no

2016-11-15

Highlights: • Valve pumping activity in A. islandica significantly increased at pH 6.2 seawater. • Changes in valve movements were not related to attempted burrowing activities. • Valve activity returned to control levels after 5 days of continuous exposure. • A. islandica tolerate pH reductions likely to follow leakage of sub-sea stored CO{sub 2}. - Abstract: Sub-sea geological storage of carbon dioxide (CO{sub 2}) provides a viable option for the Carbon Capture and Storage (CCS) approach for reducing atmospheric emissions of this greenhouse gas. Although generally considered to offer a low risk of major leakage, it remains relevant to establish the possible consequences for marine organisms that live in or on sediments overlying these storage areas if such an event may occur. The present study has used a series of laboratory exposures and behavioral bioassays to establish the sensitivity of Arctica islandica to simulated leakages of CO{sub 2}. This long-lived bivalve mollusc is widely distributed throughout the North Sea, an area where geological storage is currently taking place and where there are plans to expand this operation significantly. A recently published model has predicted a maximum drop of 1.9 pH units in seawater at the point source of a substantial escape of CO{sub 2} from sub-sea geological storage in this region. Valve movements of A. islandica exposed to reduced pH seawater were recorded continuously using Hall effect proximity sensors. Valve movement regulation is important for optimising the flow of water over the gills, which supplies food and facilitates respiration. A stepwise reduction in seawater pH showed an initial increase in both the rate and extent of valve movements in the majority of individuals tested when pH fell to 6.2 units. Exposing A. islandica to pH 6.2 seawater continuously for seven days resulted in a clear increase in valve movements during the first 40 h of exposure, followed by a gradual reduction in activity

Onshore/ Offshore Geologic Assessment for Carbon Storage in the Southeastern United States

Science.gov (United States)

Knapp, C. C.; Knapp, J. H.; Brantley, D.; Lakshmi, V.; Almutairi, K.; Almayahi, D.; Akintunde, O. M.; Ollmann, J.

2017-12-01

Eighty percent of the world's energy relies on fossil fuels and under increasingly stricter national and international regulations on greenhouse gas emissions storage of CO2 in geologic repositories seems to be not only a feasible, but also and vital solution for near/ mid-term reduction of carbon emissions. We have evaluated the feasibility of CO2 storage in saline formations of the Eastern North American Margin (ENAM) including (1) the Jurassic/Triassic (J/TR) sandstones of the buried South Georgia Rift (SGR) basin, and (2) the Mesozoic and Cenozoic geologic formations along the Mid- and South Atlantic seaboard. These analyses have included integration of subsurface geophysical data (2- and 3-D seismic surveys) with core samples, well logs as well as uses of geological databases and geospatial analysis leading to CO2 injection simulation models. ENAM is a complex and regionally extensive mature Mesozoic passive margin rift system encompassing: (1) a large volume and regional extent of related magmatism known as the Central Atlantic Magmatic Province (CAMP), (2) a complete stratigraphic column that records the post-rift evolution in several basins, (3) preserved lithospheric-scale pre-rift structures including Paleozoic sutures, and (4) a wide range of geological, geochemical, and geophysical studies both onshore and offshore. While the target reservoirs onshore show heterogeneity and a highly complex geologic evolution they also show promising conditions for significant safe CO2 storage away from the underground acquifers. Our offshore study (the Southeast Offshore Storage Resource Assessment - SOSRA) is focused on the outer continental shelf from North Carolina to the southern tip of Florida. Three old exploration wells are available to provide additional constraints on the seismic reflection profiles. Two of these wells (TRANSCO 1005-1 and COST GE-1) penetrate the pre-rift Paleozoic sedimentary formations while the EXXON 564-1 well penetrates the post

Understanding how individuals perceive carbon dioxide. Implications for acceptance of carbon dioxide capture and storage

Energy Technology Data Exchange (ETDEWEB)

Itaoka, K.; Saito, A. [Mizuho Information and Research Institute, Tokyo (Japan); Paukovic, M.; De Best-Waldhober, M. [ECN Policy Studies, Petten (Netherlands); Dowd, A.M.; Jeanneret, T.; Ashworth, P.; James, M. [The Global CCS Institute, Canberra (Australia)

2012-06-15

Carbon dioxide capture and storage (CCS) presents one potential technological solution for mitigating the atmospheric emission of carbon dioxide sources. However, CCS is a relatively new technology with associated uncertainties and perceived risks. For this reason, a growing body of research now focuses on public perceptions and potential for societal acceptance of CCS technology. Almost all explanations of CCS technology make reference to carbon dioxide, with an assumption that the general public understands CO2. It has become apparent that the general public’s knowledge and understanding of CO2’s properties influences how they engage with CO2 emitting industries and CCS technologies. However, surprisingly little research has investigated public perceptions, knowledge, and understanding of CO2. This investigation attempts to fill that gap. This report describes an investigation of how citizens of three countries (Japan, Australia, and the Netherlands) perceive CO2. Furthermore, it attempts to relate individual perceptions of CO2 to perceptions of CCS, and to determine how information provision about the underlying properties and characteristics of CO2 influences individual attitudes towards low carbon energy options, particularly CCS. In brief, the research had four ultimate aims. It aimed to: Explore the public’s knowledge and understanding of the properties of CO2; Examine the influence of that knowledge on their perceptions of CO2 and CCS; Investigate how information provision about the underlying properties and characteristics of CO2 influences individual attitudes towards CCS; and Identify if any differences between countries exist in relation to values and beliefs, knowledge of CO2’s properties, and CCS perceptions.

From Fundamental Understanding To Predicting New Nanomaterials For High Capacity Hydrogen/Methane Storage and Carbon Capture

Energy Technology Data Exchange (ETDEWEB)

Yildirim, Taner [Univ. of Pennsylvania, Philadelphia, PA (United States)

2015-03-03

On-board hydrogen/methane storage in fuel cell-powered vehicles is a major component of the national need to achieve energy independence and protect the environment. The main obstacles in hydrogen storage are slow kinetics, poor reversibility and high dehydrogenation temperatures for the chemical hydrides; and very low desorption temperatures/energies for the physisorption materials (MOF’s, porous carbons). Similarly, the current methane storage technologies are mainly based on physisorption in porous materials but the gravimetric and volumetric storage capacities are below the target values. Finally, carbon capture, a critical component of the mitigation of CO2 emissions from industrial plants, also suffers from similar problems. The solid-absorbers such as MOFs are either not stable against real flue-gas conditions and/or do not have large enough CO2 capture capacity to be practical and cost effective. In this project, we addressed these challenges using a unique combination of computational, synthetic and experimental methods. The main scope of our research was to achieve fundamental understanding of the chemical and structural interactions governing the storage and release of hydrogen/methane and carbon capture in a wide spectrum of candidate materials. We studied the effect of scaffolding and doping of the candidate materials on their storage and dynamics properties. We reviewed current progress, challenges and prospect in closely related fields of hydrogen/methane storage and carbon capture.[1-5] For example, for physisorption based storage materials, we show that tap-densities or simply pressing MOFs into pellet forms reduce the uptake capacities by half and therefore packing MOFs is one of the most important challenges going forward. For room temperature hydrogen storage application of MOFs, we argue that MOFs are the most promising scaffold materials for Ammonia-Borane (AB) because of their unique interior active metal-centers for AB binding and well

Modelling of cyclopentane promoted gas hydrate systems for carbon dioxide capture processes

DEFF Research Database (Denmark)

Herslund, Peter Jørgensen; Thomsen, Kaj; Abildskov, Jens

2014-01-01

A thermodynamic model based on the Cubic-Plus-Association equation of state and the van der Waals-Platteeuw hydrate model is applied to perform a thermodynamic evaluation of gas hydrate forming systems relevant for post-combustion carbon dioxide capture.A modelling study of both fluid phase...... behaviour and hydrate phase behaviour is presented. Cycloalkanes ranging from cyclopropane to cyclohexane, represents a challenge for CPA, both in the description of the pure component densities and for liquid-liquid equilibrium (LLE) in the binary systems with water. It is concluded that an insufficient...

The U. S. DOE Carbon Storage Program: Status and Future Directions

Science.gov (United States)

Damiani, D.

2016-12-01

The U.S. Department of Energy (DOE) is taking steps to reduce carbon dioxide (CO2) emissions through clean energy innovation, including carbon capture and storage (CCS) research. The Office of Fossil Energy Carbon Storage Program is focused on ensuring the safe and permanent storage and/or utilization of CO2 captured from stationary sources. The Program is developing and advancing geologic storage technologies both onshore and offshore that will significantly improve the effectiveness of CCS, reduce the cost of implementation, and be ready for widespread commercial deployment in the 2025-2035 timeframe. The technology development and field testing conducted through this Program will be used to benefit the existing and future fleet of fossil fuel power generating and industrial facilities by creating tools to increase our understanding of geologic reservoirs appropriate for CO2 storage and the behavior of CO2 in the subsurface. The Program is evaluating the potential for storage in depleted oil and gas reservoirs, saline formations, unmineable coal, organic-rich shale formations, and basalt formations. Since 1997, DOE's Carbon Storage Program has significantly advanced the CCS knowledge base through a diverse portfolio of applied research projects. The Core Storage R&D research component focuses on analytic studies, laboratory, and pilot- scale research to develop technologies that can improve wellbore integrity, increase reservoir storage efficiency, improve management of reservoir pressure, ensure storage permanence, quantitatively assess risks, and identify and mitigate potential release of CO2 in all types of storage formations. The Storage Field Management component focuses on scale-up of CCS and involves field validation of technology options, including large-volume injection field projects at pre-commercial scale to confirm system performance and economics. Future research involves commercial-scale characterization for regionally significant storage locations

How aware is the public of carbon capture and storage?

Energy Technology Data Exchange (ETDEWEB)

Curry, T.; Herzog, H.J. [Massachusetts Inst. of Technology, Cambridge, MA (United States). Lab. for Energy and the Environment; Reiner, D.M. [Cambridge Univ., Cambridge, (United States). Judge Inst. of Management; Ansolabehere, S. [Massachusetts Inst. of Technology, Cambridge, MA (United States). Dept. of Political Science

2005-07-01

This paper presented the results of a survey conducted in the fall of 2003 that examined attitudes toward, and understanding of, carbon dioxide capture and storage (CCS), also known as carbon sequestration. The study was conducted as part of broad range of questions about energy and the environment. The goal of the survey was to determine attitudes toward spending on the environment. In particular, the survey asked 17 questions to determine the level of public understanding of global warming and the carbon cycle and to determine public awareness of CCS. In addition to demographic information, the survey determined the effect of national energy usage information and price data on public preferences. The paper also presented some implications for public acceptance. The survey showed that the environment ranked thirteenth on a list of 22 issues facing the United States at the time of the survey, with the top three being terrorism, health care and the economy. The survey also asked respondents to choose the 2 most important of 10 environmental problems, namely water pollution, destruction of ecosystems, toxic waste, overpopulation, ozone depletion, global warming, urban sprawl, smog, endangered species, and acid rain. Global warming ranked sixth out of the issues in the survey. It was noted that very few people in the United States have heard of CCS, and those who have heard of it were no more likely to know what environmental concern it addressed than those who had not heard of CCS. 13 refs.

How aware is the public of carbon capture and storage?

International Nuclear Information System (INIS)

Curry, T.; Herzog, H.J.; Reiner, D.M.; Ansolabehere, S.

2005-01-01

This paper presented the results of a survey conducted in the fall of 2003 that examined attitudes toward, and understanding of, carbon dioxide capture and storage (CCS), also known as carbon sequestration. The study was conducted as part of broad range of questions about energy and the environment. The goal of the survey was to determine attitudes toward spending on the environment. In particular, the survey asked 17 questions to determine the level of public understanding of global warming and the carbon cycle and to determine public awareness of CCS. In addition to demographic information, the survey determined the effect of national energy usage information and price data on public preferences. The paper also presented some implications for public acceptance. The survey showed that the environment ranked thirteenth on a list of 22 issues facing the United States at the time of the survey, with the top three being terrorism, health care and the economy. The survey also asked respondents to choose the 2 most important of 10 environmental problems, namely water pollution, destruction of ecosystems, toxic waste, overpopulation, ozone depletion, global warming, urban sprawl, smog, endangered species, and acid rain. Global warming ranked sixth out of the issues in the survey. It was noted that very few people in the United States have heard of CCS, and those who have heard of it were no more likely to know what environmental concern it addressed than those who had not heard of CCS. 13 refs

Inorganic membranes for carbon capture and power generation

Science.gov (United States)

Snider, Matthew T.

Inorganic membranes are under consideration for cost-effective reductions of carbon emissions from coal-fired power plants, both in the capture of pollutants post-firing and in the direct electrochemical conversion of coal-derived fuels for improved plant efficiency. The suitability of inorganic membrane materials for these purposes stems as much from thermal and chemical stability in coal plant operating conditions as from high performance in gas separations and power generation. Hydrophilic, micro-porous zeolite membrane structures are attractive for separating CO2 from N2 in gaseous waste streams due to the attraction of CO2 to the membrane surface and micropore walls that gives the advantage to CO2 transport. Recent studies have indicated that retention of the templating agent used in zeolite synthesis can further block N2 from the micropore interior and significantly improve CO2/N2 selectivity. However, the role of the templating agent in micro-porous transport has not been well investigated. In this work, gas sorption studies were conducted by high-pressure thermo-gravimetric analysis on Zeolite Y membrane materials to quantify the effect of the templating agent on CO2, N2, and H2O adsorption/desorption, as well as to examine the effect of humidification on overall membrane performance. In equilibrium conditions, the N2 sorption enthalpy was nearly unchanged by the presence of the templating agent, but the N2 pore occupation was reduced ˜1000x. Thus, the steric nature of the blocking of N2 from the micropores by the templating agent was confirmed. CO2 and H2O sorption enthalpies were similarly unaffected by the templating agent, and the micropore occupations were only reduced as much as the void volume taken up by the templating agent. Thus, the steric blocking effect did not occur for molecules more strongly attracted to the micropore walls. Additionally, in time-transient measurements the CO 2 and H2O mobilities were significantly enhanced by the presence

Evolution and Adaptation of Phytoplankton Photosynthetic Pathways to perturbations of the geological carbon system

Science.gov (United States)

Rickaby, R. E.; Young, J. N.; Hermoso, M.; Heureux, A.; McCLelland, H.; Lee, R.; Eason Hubbard, M.

2012-12-01

The ocean and atmosphere carbon system has varied greatly over geological history both in response to initial evolutionary innovation, and as a driver of adaptive change. Here we establish that positive selection in Rubisco, the most abundant enzyme on the Earth responsible for all photosynthetic carbon fixation, occurred early in Earth's history, and basal to the radiation of the modern marine algal groups. Our signals of positive selection appear to be triggered by changing intracellular concentrations of carbon dioxide (CO2) due to the emergence of carbon concentrating mechanisms between 1.56 and 0.41 Ba in response to declining atmospheric CO2 . We contend that, at least in terms of carbon, phytoplankton generally were well poised to manage subsequent abrupt carbon cycle perturbations. The physiological pathways for optimising carbon acquisition across a wide range of ambient carbon dioxide concentrations had already been established and were genetically widespread across open ocean phytoplankton groups. We will further investigate some case studies from the Mesozoic and Cenozoic abrupt carbon cycle excursions using isotopic tools to probe the community photosynthetic response and demonstrate the flexibility of phytoplankton photosynthesis in the face of major perturbations. In particular, an unprecedented resolution record across the Toarcian (Early Jurassic) carbon isotope excursion in the Paris Basin reveals a selection and evolution towards a community reliant solely on diffusive carbon dioxide supply for photosynthesis at the height of the excursion at 1500-2500 ppm CO2. The continued flourishing of the phytoplankton biological pump throughout this excursion was able to remove the excess carbon injected into the water column in less than 45 kyrs.

Pilot-Scale Silicone Process for Low-Cost Carbon Dioxide Capture

Energy Technology Data Exchange (ETDEWEB)

Farnum, Rachel; Perry, Robert; Wood, Benjamin

2014-12-31

GE Global Research is developing technology to remove carbon dioxide (CO 2) from the flue gas of coal-fired powerplants. A mixture of 3-aminopropyl end-capped polydimethylsiloxane (GAP-1m) and triethylene glycol (TEG) is the preferred CO2-capture solvent. GE Global Research was contracted by the Department of Energy to test a pilot-scale continuous CO2 absorption/desorption system using a GAP-1m/TEG mixture as the solvent. As part of that effort, an Environmental, Health, and Safety (EH&S) assessment for a CO2-capture system for a 550 MW coal-fired powerplant was conducted. Five components of the solvent, CAS#2469-55-8 (GAP-0), CAS#106214-84-0 (GAP-1-4), TEG, and methanol and xylene (minor contaminants from the aminosilicone) are included in this assessment. One by-product, GAP- 1m/SOX salt, and dodecylbenzenesulfonicacid (DDBSA) were also identified foranalysis. An EH&S assessment was also completed for the manufacturing process for the GAP-1m solvent. The chemicals associated with the manufacturing process include methanol, xylene, allyl chloride, potassium cyanate, sodium hydroxide (NaOH), tetramethyldisiloxane (TMDSO), tetramethyl ammonium hydroxide, Karstedt catalyst, octamethylcyclotetrasiloxane (D4), Aliquat 336, methyl carbamate, potassium chloride, trimethylamine, and (3-aminopropyl) dimethyl silanol. The toxicological effects of each component of both the CO2 capture system and the manufacturing process were defined, and control mechanisms necessary to comply with U.S. EH&S regulations are summarized. Engineering and control systems, including environmental abatement, are described for minimizing exposure and release of the chemical components. Proper handling and storage recommendations are made for each chemical to minimize risk to workers and the surrounding community.

'Capture ready' regulation of fossil fuel power plants - Betting the UK's carbon emissions on promises of future technology

International Nuclear Information System (INIS)

Markusson, Nils; Haszeldine, Stuart

2010-01-01

Climate change legislation requires emissions reductions, but the market shows interest in investing in new fossil fuelled power plants. The question is whether capture ready policy can reconcile these interests. The term 'capture ready' has been used a few years by the UK Government when granting licences for fossil fuelled power plants, but only recently has the meaning of the term been defined. The policy has been promoted as a step towards CCS and as an insurance against carbon lock-in. This paper draws on literature on technology lock-in and on regulation of technology undergoing development. Further, versions of the capture readiness concept proposed to date are compared. Capture readiness requirements beyond the minimum criterion of space on the site for capture operations are explored. This includes integration of capture and power plant, downstream operations, overall system integration and regulation of future retrofitting. Capture readiness comes with serious uncertainties and is no guarantee that new-built fossil plants will be abatable or abated in the future. As a regulatory strategy, it has been over-promised in the UK.

Micro-Encapsulation of non-aqueous solvents for energy-efficient carbon capture

Energy Technology Data Exchange (ETDEWEB)

Stolaroff, Joshua K; Ye, Congwang; Oakdale, James [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Baker, Sarah; Nugyen, Du; Smith, William; Aines, Roger

2016-11-14

Here, we demonstrate micro-encapsulation of several promising designer solvents: an IL, PCIL, and CO2BOL. We develop custom polymers that cure by UV light in the presence of each solvent while maintaining high CO2 permeability. We use several new process strategies to accommodate the viscosity and phase changes. We then measure and compare the CO2 absorption rate and capacity as well as the multi-cycle performance of the encapsulated solvents. These results are compared with previous work on encapsulated sodium carbonate solution. The prospects for designer solvents to reduce the cost of post-combustion capture and the implications for process design with encapsulated solvents are discussed.

EVALUATION OF CARBON DIOXIDE CAPTURE FROM EXISTING COAL FIRED PLANTS BY HYBRID SORPTION USING SOLID SORBENTS

Energy Technology Data Exchange (ETDEWEB)

Benson, Steven; Browers, Bruce; Srinivasachar, Srivats; Laudal, Daniel

2014-12-31

Under contract DE-FE0007603, the University of North Dakota conducted the project Evaluation of Carbon Dioxide Capture from Existing Coal Fired Plants by Hybrid Sorption Using Solid Sorbents. As an important element of this effort, a Technical and Economic Feasibility Study was conducted by Barr Engineering Co. (Barr) in association with the University of North Dakota. The assessment developed a process flow diagram, major equipment list, heat balances for the SCPC power plant, capital cost estimate, operating cost estimate, levelized cost of electricity, cost of CO2 capture ($/ton) and three sensitivity cases for the CACHYS™ process.

Development and Implementation of the Midwest Geological Sequestration Consortium CO₂-Technology Transfer Center

Energy Technology Data Exchange (ETDEWEB)

Greenberg, Sallie E. [Univ. of Illinois, Champaign, IL (United States)

2015-06-30

In 2009, the Illinois State Geological Survey (ISGS), in collaboration with the Midwest Geological Sequestration Consortium (MGSC), created a regional technology training center to disseminate carbon capture and sequestration (CCS) technology gained through leadership and participation in regional carbon sequestration projects. This technology training center was titled and branded as the Sequestration Training and Education Program (STEP). Over the last six years STEP has provided local, regional, national, and international education and training opportunities for engineers, geologists, service providers, regulators, executives, K-12 students, K-12 educators, undergraduate students, graduate students, university and community college faculty members, and participants of community programs and functions, community organizations, and others. The goal for STEP educational programs has been on knowledge sharing and capacity building to stimulate economic recovery and development by training personnel for commercial CCS projects. STEP has worked with local, national and international professional organizations and regional experts to leverage existing training opportunities and provide stand-alone training. This report gives detailed information on STEP activities during the grant period (2009-2015).

CO{sub 2}-capture in coal based IGCC power plants

Energy Technology Data Exchange (ETDEWEB)

Van Aart, F.; Fleuren, W.; Kamphuis, H.; Ploumen, P.; Jelles, S. [KEMA, Arnhem (Netherlands)

2007-07-01

The paper discusses IGCC with carbon capture and storage (CCS), both for retrofit and capture ready plants. The penalties for carbon dioxide capture are given, along with its effect on CAPEX and OPEC costs. 3 refs., 9 figs.

Characterization of Qatar's surface carbonates for CO2 capture and thermochemical energy storage

Science.gov (United States)

Kakosimos, Konstantinos E.; Al-Haddad, Ghadeer; Sakellariou, Kyriaki G.; Pagkoura, Chrysa; Konstandopoulos, Athanasios G.

2017-06-01

Samples of surface carbonates were collected from three different areas of the Qatar peninsula. We employed material characterization techniques to examine the morphology and composition of the samples, while their CO2 capture capacity was assessed via multiple successive calcination-carbonation cycles. Our samples were mainly calcite and dolomite based. Calcite samples showed higher initial capacity of around 11 mmol CO2 g-1 which decayed rapidly to less than 2 mmol CO2 g-1. On the other hand, dolomite samples showed an excellent stability (˜15 cycles) with a capacity of 6 mmol CO2 g-1. The performance of the dolomite samples is better compared to other similar natural samples, from literature. A promising result for future studies towards improving their performance by physical and chemical modification.

Covalent organic polymer functionalized activated carbon: A novel material for water contaminant removal and CO2 capture

DEFF Research Database (Denmark)

Mines, Paul D.; Thirion, Damien; Uthuppu, Basil

Covalent organic polymers (COPs) have emerged as one of the leading advanced materials for environmental applications, such as the capture and recovery of carbon dioxide and the removal of contaminants from polluted water. COPs exhibit many remarkable properties that other leading advanced materi...

Establishing MICHCARB, a geological carbon sequestration research and education center for Michigan, implemented through the Michigan Geological Repository for Research and Education, part of the Department of Geosciences at Western Michigan University

Energy Technology Data Exchange (ETDEWEB)

Barnes, David A. [Western Michigan Univ., Kalamazoo MI (United States); Harrison, William B. [Western Michigan Univ., Kalamazoo MI (United States)

2014-01-28

The Michigan Geological Repository for Research and Education (MGRRE), part of the Department of Geosciences at Western Michigan University (WMU) at Kalamazoo, Michigan, established MichCarb—a geological carbon sequestration resource center by: • Archiving and maintaining a current reference collection of carbon sequestration published literature • Developing statewide and site-specific digital research databases for Michigan’s deep geological formations relevant to CO2 storage, containment and potential for enhanced oil recovery • Producing maps and tables of physical properties as components of these databases • Compiling all information into a digital atlas • Conducting geologic and fluid flow modeling to address specific predictive uses of CO2 storage and enhanced oil recovery, including compiling data for geological and fluid flow models, formulating models, integrating data, and running the models; applying models to specific predictive uses of CO2 storage and enhanced oil recovery • Conducting technical research on CO2 sequestration and enhanced oil recovery through basic and applied research of characterizing Michigan oil and gas and saline reservoirs for CO2 storage potential volume, injectivity and containment. Based on our research, we have concluded that the Michigan Basin has excellent saline aquifer (residual entrapment) and CO2/Enhanced oil recovery related (CO2/EOR; buoyant entrapment) geological carbon sequestration potential with substantial, associated incremental oil production potential. These storage reservoirs possess at least satisfactory injectivity and reliable, permanent containment resulting from associated, thick, low permeability confining layers. Saline aquifer storage resource estimates in the two major residual entrapment, reservoir target zones (Lower Paleozoic Sandstone and Middle Paleozoic carbonate and sandstone reservoirs) are in excess of 70-80 Gmt (at an overall 10% storage efficiency factor; an approximately

Carbon balance of CO2-EOR for NCNO classification

Energy Technology Data Exchange (ETDEWEB)

Nunez-Lopez, Vanessa [The University of Texas at Austin; Gil-Egui, Ramon; Gonzalez-Nicolas, Ana; Hovorka, Susan D

2017-03-18

The question of whether carbon dioxide enhanced oil recovery (CO2-EOR) constitutes a valid alternative for greenhouse gas emission reduction has been frequently asked by the general public and environmental sectors. Through this technology, operational since 1972, oil production is enhanced by injecting CO2 into depleted oil reservoirs in order displace the residual oil toward production wells in a solvent/miscible process. For decades, the CO2 utilized for EOR has been most commonly sourced from natural CO2 accumulations. More recently, a few projects have emerged where anthropogenic CO2 (A-CO2) is captured at an industrial facility, transported to a depleted oil field, and utilized for EOR. If carbon geologic storage is one of the project objectives, all the CO2 injected into the oil field for EOR could technically be stored in the formation. Even though the CO2 is being prevented from entering the atmosphere, and permanently stored away in a secured geologic formation, a question arises as to whether the total CO2 volumes stored in order to produce the incremental oil through EOR are larger than the CO2 emitted throughout the entire CO2-EOR process, including the capture facility, the EOR site, and the refining and burning of the end product. We intend to answer some of these questions through a DOE-NETL funded study titled “Carbon Life Cycle Analysis of CO2-EOR for Net Carbon Negative Oil (NCNO) Classification”. NCNO is defined as oil whose carbon emissions to the atmosphere, when burned or otherwise used, are less than the amount of carbon permanently stored in the reservoir in order to produce the oil. In this paper, we focus on the EOR site in what is referred to as a gate-to-gate system, but are inclusive of the burning of the refined product, as this end member is explicitly stated in the definition of NCNO. Finally, we use Cranfield, Mississippi, as a case study and come to the conclusion that the incremental oil produced is net carbon negative.

INTEGRATED GEOLOGIC-ENGINEERING MODEL FOR REEF AND CARBONATE SHOAL RESERVOIRS ASSOCIATED WITH PALEOHIGHS: UPPER JURASSIC SMACKOVER FORMATION, NORTHEASTERN GULF OF MEXICO

Energy Technology Data Exchange (ETDEWEB)

Ernest A. Mancini

2002-09-25

The University of Alabama in cooperation with Texas A&M University, McGill University, Longleaf Energy Group, Strago Petroleum Corporation, and Paramount Petroleum Company are undertaking an integrated, interdisciplinary geoscientific and engineering research project. The project is designed to characterize and model reservoir architecture, pore systems and rock-fluid interactions at the pore to field scale in Upper Jurassic Smackover reef and carbonate shoal reservoirs associated with varying degrees of relief on pre-Mesozoic basement paleohighs in the northeastern Gulf of Mexico. The project effort includes the prediction of fluid flow in carbonate reservoirs through reservoir simulation modeling which utilizes geologic reservoir characterization and modeling and the prediction of carbonate reservoir architecture, heterogeneity and quality through seismic imaging. The primary objective of the project is to increase the profitability, producibility and efficiency of recovery of oil from existing and undiscovered Upper Jurassic fields characterized by reef and carbonate shoals associated with pre-Mesozoic basement paleohighs. The principal research effort for Year 2 of the project has been reservoir characterization, 3-D modeling and technology transfer. This effort has included six tasks: (1) the study of rockfluid interactions, (2) petrophysical and engineering characterization, (3) data integration, (4) 3-D geologic modeling, (5) 3-D reservoir simulation and (6) technology transfer. This work was scheduled for completion in Year 2. Overall, the project work is on schedule. Geoscientific reservoir characterization is essentially completed. The architecture, porosity types and heterogeneity of the reef and shoal reservoirs at Appleton and Vocation Fields have been characterized using geological and geophysical data. The study of rock-fluid interactions is near completion. Observations regarding the diagenetic processes influencing pore system development and

Carbon Issues Task Force Report for the Idaho Strategic Energy Alliance

Energy Technology Data Exchange (ETDEWEB)

Travis L. Mcling

2010-10-01

The Carbon Issues Task Force has the responsibility to evaluate emissions reduction and carbon offset credit options, geologic carbon sequestration and carbon capture, terrestrial carbon sequestration on forest lands, and terrestrial carbon sequestration on agricultural lands. They have worked diligently to identify ways in which Idaho can position itself to benefit from potential carbon-related federal legislation, including identifying opportunities for Idaho to engage in carbon sequestration efforts, barriers to development of these options, and ways in which these barriers can be overcome. These are the experts to which we will turn when faced with federal greenhouse gas-related legislation and how we should best react to protect and provide for Idaho’s interests. Note that the conclusions and recommended options in this report are not intended to be exhaustive, but rather form a starting point for an informed dialogue regarding the way-forward in developing Idaho energy resources.

CO{sub 2} CAPTURE BY ABSORPTION WITH POTASSIUM CARBONATE

Energy Technology Data Exchange (ETDEWEB)

Gary T. Rochelle; J.Tim Cullinane; Marcus Hilliard; Eric Chen; Babatunde Oyenekan; Ross Dugas

2005-01-31

The objective of this work is to improve the process for CO{sub 2} capture by alkanolamine absorption/stripping by developing an alternative solvent, aqueous K{sub 2}CO{sub 3} promoted by piperazine. Thermodynamic modeling predicts that the heat of desorption of CO{sub 2} from 5m K+/2.5 PZ from 85 kJ/mole at 40 C to 30 kJ/mole at 120 C. Mass transfer modeling of this solvent suggests that carbonate and general salt concentration play a major role in catalyzing the rate of reaction of CO{sub 2} with piperazine. Stripper modeling suggests that with the multipressure stripper, the energy consumption with a generic solvent decreases by 15% as the heat of desorption is decreased from 23.8 to 18.5 kcal/gmol. A second pilot plant campaign with 5m K+/2.5 PZ was successfully completed.

Bench-scale studies on capture of mercury on mineral non-carbon based sorbents

Energy Technology Data Exchange (ETDEWEB)

Li, Yang [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion; Utah Univ., Salt Lake City, UT (United States). Dept. of Chemical Engineering; Wendt, Jost O.L. [Utah Univ., Salt Lake City, UT (United States). Dept. of Chemical Engineering; Zhang, Junying; Zheng, Chuguang [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion

2013-07-01

A new high-temperature, mineral non-carbon based dispersed sorbent derived from paper recycling products has been shown to capture mercury at high temperatures in excess of 600 C. The sorbent is consisted of kaolinite/calcite/lime mixtures. Experiments have been conducted on chemi-sorption of elemental mercury in air on a packed bed. The sorption occurs at temperatures between 600 and 1,100 C and requires activation of the minerals contained within the sorbents. Mercury capture is dominated by temperature and capture on sorbents over long time scales. The capture shows a maximum effectiveness at 1,000 C and increases monotonically with temperature. The presence of oxygen is also the required. Freshly activated sorbent is the most effective, and deactivation of sorbents occurs at high temperatures with long pre-exposure times. This activation is suspected to involve a solid-solid reaction between intimately mixed calcium oxide and silica that are both contained within the sorbent. Deactivation occurs at temperatures higher than 1,000 C, and this is due to melting of the substrate and pore closure. The situation in packed beds is complicated because the bed also shrinks, thus allowing channeling and by-passing, and consequent ambiguities in determining sorbent saturation. Sorbent A had significantly greater capacity for mercury sorption than did Sorbent B, for all temperatures and exposure time examined. The effect of SiO{sub 2} on poor Sorbent B is much larger than sorbent A.

Updated (BP3) Technical and Economic Feasibility Study - Electrochemical Membrane for Carbon Dioxide Capture and Power Generation

Energy Technology Data Exchange (ETDEWEB)

Ghezel-Ayagh, Hossein [FuelCell Energy, Inc., Danbury, CT (United States)

2017-12-21

This topical report summarizes the results of an updated Technical & Economic Feasibility Study (T&EFS) which was conducted in Budget Period 3 of the project to evaluate the performance and cost of the Electrochemical Membrane (ECM)-based CO₂ capture system. The ECM technology is derived from commercially available inorganic membranes; the same used in FuelCell Energy’s commercial fuel cell power plants and sold under the trade name Direct FuelCell® (DFC®). The ECM stacks are utilized in the Combined Electric Power (generation) And Carbon dioxide Separation (CEPACS) systems which can be deployed as add-ons to conventional power plants (Pulverized Coal, Combined Cycle, etc.) or industrial facilities to simultaneously produce power while capturing >90% of the CO₂ from the flue gas. In this study, an ECM-based CEPACS plant was designed to capture and compress >90% of the CO₂ (for sequestration or beneficial use) from the flue gas of a reference 550 MW (nominal, net AC) Pulverized Coal (PC) Rankine Cycle (Subcritical steam) power plant. ECM performance was updated based on bench scale ECM stack test results. The system process simulations were performed to generate the CEPACS plant performance estimates. The performance assessment included estimation of the parasitic power consumption for CO₂ capture and compression, and the efficiency impact on the PC plant. While the ECM-based CEPACS system for the 550 MW PC plant captures 90% of CO₂ from the flue gas, it generates additional (net AC) power after compensating for the auxiliary power requirements of CO₂ capture and compression. An equipment list, ECM stacks packaging design, and CEPACS plant layout were developed to facilitate the economic analysis. Vendor quotes were also solicited. The economic feasibility study included estimation of CEPACS plant capital cost, cost of electricity (COE) analyses and estimation of cost per ton of CO₂

Post-combustion CO2 capture with activated carbons using fixed bed adsorption

Science.gov (United States)

Al Mesfer, Mohammed K.; Danish, Mohd; Fahmy, Yasser M.; Rashid, Md. Mamoon

2018-03-01

In the current work, the capturing of carbon dioxide from flue gases of post combustion emission using fixed bed adsorption has been carried out. Two grades of commercial activated carbon (sorbent-1 and sorbent-2) were used as adsorbent. Feed consisting of CO2 and N2 mixture was used for carrying out the adsorption. The influence of bed temperature, feed rate, equilibrium partial pressure and initial % CO2 in feed were considered for analyzing adsorption-desorption process. It was found that the total adsorption-desorption cycle time decreases with increased column temperature and feed rates. The time required to achieve the condition of bed saturation decreases with increased bed temperature and feed rates. The amount of CO2 adsorbed/Kg of the adsorbent declines with increased bed temperature with in studied range for sorbent-1 and sorbent-2. It was suggested that the adsorption capacity of the both the sorbents increases with increased partial pressure of the gas.

A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

DEFF Research Database (Denmark)

Bonalumi, Davide; Valenti, Gianluca; Lillia, Stefano

2016-01-01

Post-combustion carbon capture technologies seem to be necessary to realize the CO2 mitigation policies internationally shared for the next future, despite none of them appears to be ready for full-scale applications. This work considers the aqueous ammonia based process for a coal-fired Ultra....... The second layout operates at cooled conditions, which does not yield any salt precipitation. The Chilled layout reveals low specific heat duty and SPECCA equal to 2.2 and 2.86 MJ/kgco2, respectively. In contrast, the Cooled layout presents a higher specific heat duty of almost 3 MJ/kgco2 but, importantly...

Novel porous carbon materials with ultrahigh nitrogen contents for selective CO 2 capture

KAUST Repository

Zhao, Yunfeng; Zhao, Lan; Yao, Kexin; Yang, Yang; Zhang, Qiang; Han, Yu

2012-01-01

Nitrogen-doped carbon materials were prepared by a nanocasting route using tri-continuous mesoporous silica IBN-9 as a hard template. Rationally choosing carbon precursors and carefully controlling activation conditions result in an optimized material denoted as IBN9-NC1-A, which possesses a very high nitrogen doping concentration (∼13 wt%) and a large surface area of 890 m 2 g -1 arising from micropores (<1 nm). It exhibits an excellent performance for CO 2 adsorption over a wide range of CO 2 pressures. Specifically, its equilibrium CO 2 adsorption capacity at 25 °C reaches up to 4.50 mmol g -1 at 1 bar and 10.53 mmol g -1 at 8 bar. In particular, it shows a much higher CO 2 uptake at low pressure (e.g. 1.75 mmol g -1 at 25 °C and 0.2 bar) than any reported carbon-based materials, owing to its unprecedented nitrogen doping level. The high nitrogen contents also give rise to significantly enhanced CO 2/N 2 selectivities (up to 42), which combined with the high adsorption capacities, make these new carbon materials promising sorbents for selective CO 2 capture from power plant flue gas and other relevant applications. © 2012 The Royal Society of Chemistry.

Carbon dioxide (CO2) capture and storage : Canadian market development

International Nuclear Information System (INIS)

Hendriks, A.

2006-01-01

Carbon dioxide (CO 2 ) enhanced oil recovery (EOR) is used to extend the life of light oil reservoirs in Canada. An additional 13 per cent of original oil in place is typically recovered using CO 2 flooding processes. However, a carbon capture and storage (CCS) market is needed in order to commercialize CO 2 flooding technologies. CO 2 can be obtained from naturally-occurring accumulations in underground reservoirs, electrical and coal-fired generation plants, petrochemical facilities, and upstream oil and gas processing facilities. CO 2 is sequestered in EOR processes, in sour gas disposal processes, solvent recovery processes, and in coalbed methane (CBM) extraction. It is also disposed in depleted fields and aquifers. While CCS technologies are mature, project economics remain marginal. However, CCS in EOR is commercially feasible at current high oil prices. No transportation infrastructure is in place to transport sources of CO 2 in the high volumes needed to establish a market. While governments have created a favourable public policy environment for CCS, governments will need to address issues related to infrastructure, public perception of CCS, and stakeholder engagement with CCS projects. It was concluded that CCS and CO 2 flooding techniques have the capacity to reduce greenhouse gas (GHG) emissions while helping to sustain light oil production. tabs., figs

Biomass waste carbon materials as adsorbents for CO2 capture under post-combustion conditions

Directory of Open Access Journals (Sweden)

Elisa M Calvo-Muñoz

2016-05-01

Full Text Available A series of porous carbon materials obtained from biomass waste have been synthesized, with different morphologies and structural properties, and evaluated as potential adsorbents for CO2 capture in post-combustion conditions. These carbon materials present CO2 adsorption capacities, at 25 ºC and 101.3 kPa, comparable to those obtained by other complex carbon or inorganic materials. Furthermore, CO2 uptakes under these conditions can be well correlated to the narrow micropore volume, derived from the CO2 adsorption data at 0 ºC (VDRCO2. In contrast, CO2 adsorption capacities at 25 ºC and 15 kPa are more related to only pores of sizes lower than 0.7 nm. The capacity values obtained in column adsorption experiments were really promising. An activated carbon fiber obtained from Alcell lignin, FCL, presented a capacity value of 1.3 mmol/g (5.7 %wt. Moreover, the adsorption capacity of this carbon fiber was totally recovered in a very fast desorption cycle at the same operation temperature and total pressure and, therefore, without any additional energy requirement. Thus, these results suggest that the biomass waste used in this work could be successfully valorized as efficient CO2 adsorbent, under post-combustion conditions, showing excellent regeneration performance.

Production of sustainable methane from renewable energy and captured carbon dioxide with the use of Solid Oxide Electrolyzer: A thermodynamic assessment

International Nuclear Information System (INIS)

Stempien, Jan Pawel; Ni, Meng; Sun, Qiang; Chan, Siew Hwa

2015-01-01

A possible pathway for renewable and sustainable methane production from captured carbon dioxide, water (or seawater) and renewable electricity is proposed and analysed. The proposed system includes Solid Oxide Electrolyzer Cell combined with ex-situ methane synthesis reactor comprising Sabatier, Methanation and Water-Gas Shift reactions. A well validated electrochemical model is used to describe the behaviour of the electrolyzer for steam/carbon dioxide co-electrolysis. The methane synthesis reactor is modelled by a set of equations based on thermodynamic equilibrium reaction constants. Effects of current density, temperature, pressure and initial steam to carbon dioxide ratio on system performance are analysed and their effects are discussed. It is found that a simple, single-pass system without heat recuperation could achieve a maximum overall energy efficiency of 60.87% (based on lower heating value), a maximum electrical energy efficiency of 81.08% (based on lower heating value), and a maximum amount of methane production of ∼1.52 Nm 3  h −1  m −2 of electrolyzer. It is also found that conversion of ∼100% captured carbon dioxide is possible in the proposed system. - Highlights: • Analysis of Solid Oxide Electrolyzer combined with methane synthesis process. • Efficiency of converting water and carbon dioxide into synthetic, renewable methane above 81%. • Effects of process temperature, pressure, gas flux and compositions were analysed. • Methane production of ∼1.52 [Nm 3 h −1 m −2 of electrolyzer]. • Conversion of ∼100% of captured CO 2 is possible

The NatCarb geoportal: Linking distributed data from the Carbon Sequestration Regional Partnerships

Science.gov (United States)

Carr, T.R.; Rich, P.M.; Bartley, J.D.

2007-01-01

The Department of Energy (DOE) Carbon Sequestration Regional Partnerships are generating the data for a "carbon atlas" of key geospatial data (carbon sources, potential sinks, etc.) required for rapid implementation of carbon sequestration on a broad scale. The NATional CARBon Sequestration Database and Geographic Information System (NatCarb) provides Web-based, nation-wide data access. Distributed computing solutions link partnerships and other publicly accessible repositories of geological, geophysical, natural resource, infrastructure, and environmental data. Data are maintained and enhanced locally, but assembled and accessed through a single geoportal. NatCarb, as a first attempt at a national carbon cyberinfrastructure (NCCI), assembles the data required to address technical and policy challenges of carbon capture and storage. We present a path forward to design and implement a comprehensive and successful NCCI. ?? 2007 The Haworth Press, Inc. All rights reserved.

News Media Analysis of Carbon Capture and Storage and Biomass: Perceptions and Possibilities

Directory of Open Access Journals (Sweden)

Andrea M. Feldpausch-Parker

2015-04-01

Full Text Available In the US, carbon capture and storage (CCS has received most of its attention when coupled with the fossil fuel industry as a mitigation strategy for climate change. CCS, which is constituted as a broad suite of capture and sequestration technologies and techniques, does not preclude coupling with other energy industries such as bioenergy (bioenergy and CCS or BECCS. In this paper, we examined news media coverage of CCS and biomass individually in locations throughout the US where these technologies are being explored to determine how they are perceived and what possibilities lay in their coupling for climate change mitigation. From our analyses, we found that individually, both CCS and biomass are perceived generally as beneficial for energy development by the news media, though they are not often mentioned in combination. Combined references do, however, speak to their value for climate change mitigation and as an alternative to fossil fuels.

New Class of Hybrid Materials for Detection, Capture, and "On-Demand" Release of Carbon Monoxide.

Science.gov (United States)

Pitto-Barry, Anaïs; Lupan, Alexandru; Ellingford, Christopher; Attia, Amr A A; Barry, Nicolas P E

2018-04-25

Carbon monoxide (CO) is both a substance hazardous to health and a side product of a number of industrial processes, such as methanol steam reforming and large-scale oxidation reactions. The separation of CO from nitrogen (N 2 ) in industrial processes is considered to be difficult because of the similarities of their electronic structures, sizes, and physicochemical properties (e.g., boiling points). Carbon monoxide is also a major poison in fuel cells because of its adsorption onto the active sites of the catalysts. It is therefore of the utmost economic importance to discover new materials that enable effective CO capture and release under mild conditions. However, methods to specifically absorb and easily release CO in the presence of contaminants, such as water, nitrogen, carbon dioxide, and oxygen, at ambient temperature are not available. Here, we report the simple and versatile fabrication of a new class of hybrid materials that allows capture and release of carbon monoxide under mild conditions. We found that carborane-containing metal complexes encapsulated in networks made of poly(dimethylsiloxane) react with CO, even when immersed in water, leading to dramatic color and infrared signature changes. Furthermore, we found that the CO can be easily released from the materials by simply dipping the networks into an organic solvent for less than 1 min, at ambient temperature and pressure, which not only offers a straightforward recycling method, but also a new method for the "on-demand" release of carbon monoxide. We illustrated the utilization of the on-demand release of CO from the networks by carrying out a carbonylation reaction on an electron-deficient metal complex that led to the formation of the CO-adduct, with concomitant recycling of the gel. We anticipate that our sponge-like materials and scalable methodology will open up new avenues for the storage, transport, and controlled release of CO, the silent killer and a major industrial poison.

Geologic Interpretation of Data Sets Collected by Planetary Analog Geology Traverses and by Standard Geologic Field Mapping. Part 1; A Comparison Study

Science.gov (United States)

Eppler, Dean B.; Bleacher, Jacob F.; Evans, Cynthia A.; Feng, Wanda; Gruener, John; Hurwitz, Debra M.; Skinner, J. A., Jr.; Whitson, Peggy; Janoiko, Barbara

2013-01-01

Geologic maps integrate the distributions, contacts, and compositions of rock and sediment bodies as a means to interpret local to regional formative histories. Applying terrestrial mapping techniques to other planets is challenging because data is collected primarily by orbiting instruments, with infrequent, spatiallylimited in situ human and robotic exploration. Although geologic maps developed using remote data sets and limited "Apollo-style" field access likely contain inaccuracies, the magnitude, type, and occurrence of these are only marginally understood. This project evaluates the interpretative and cartographic accuracy of both field- and remote-based mapping approaches by comparing two 1:24,000 scale geologic maps of the San Francisco Volcanic Field (SFVF), north-central Arizona. The first map is based on traditional field mapping techniques, while the second is based on remote data sets, augmented with limited field observations collected during NASA Desert Research & Technology Studies (RATS) 2010 exercises. The RATS mission used Apollo-style methods not only for pre-mission traverse planning but also to conduct geologic sampling as part of science operation tests. Cross-comparison demonstrates that the Apollo-style map identifies many of the same rock units and determines a similar broad history as the field-based map. However, field mapping techniques allow markedly improved discrimination of map units, particularly unconsolidated surficial deposits, and recognize a more complex eruptive history than was possible using Apollo-style data. Further, the distribution of unconsolidated surface units was more obvious in the remote sensing data to the field team after conducting the fieldwork. The study raises questions about the most effective approach to balancing mission costs with the rate of knowledge capture, suggesting that there is an inflection point in the "knowledge capture curve" beyond which additional resource investment yields progressively

Summary of Carbon Storage Incentives and Potential Legislation: East Sub-Basin Project Task 3.1 Business and Financial Case Study

Energy Technology Data Exchange (ETDEWEB)

Trabucchi, Chiara [Industrial Economics, Incorporated

2018-05-16

The CarbonSAFE Illinois – East Sub-Basin project is conducting a pre-feasibility assessment for commercial-scale CO2 geological storage complexes. The project aims to identify sites capable of storing more than 50 million tons of industrially-sourced CO2. To support the business development assessment of the economic viability of potential sites in the East Sub-Basin and explore conditions under which a carbon capture and storage (CCS) project therein might be revenue positive, this document provides a summary of carbon storage incentives and legislation of potential relevance to the project.

Convenient and large-scale synthesis of nitrogen-rich hierarchical porous carbon spheres for supercapacitors and CO2 capture

Science.gov (United States)

Chang, Binbin; Zhang, Shouren; Yin, Hang; Yang, Baocheng

2017-08-01

Herein, considering the great potential of nitrogen-doped hierarchical porous carbons in energy storage and CO2 capture, we designed a convenient and easily large-scale production strategy for preparing nitrogen-doped hierarchical porous carbon sphere (NHPCS) materials. In this synthesis route, spherical resorcinol-formaldehyde (RF) resins were selected as carbon precursor, and then the ZnCl2-impregnated RF resin spheres were carbonized in a NH3 atmosphere at a temperature range of 600-800 °C. During the one-step heat-treatment process, nitrogen atom could be efficiently incorporated into the carbon skeleton, and the interconnected and hierarchical pore structure with different micro/mesopore proportion could be generated and tuned by adjusting the activating agent ZnCl2 dosage and carbonization temperature. The resultant nitrogen-doped hierarchical porous carbon sphere materials exhibited a satisfactory charge storage capacity, and the optimal sample of NHPCS-2-8 with a high mesopore proportion obtained at 800 °C with a ZnCl2/RF mass ratio of 2:1 presented a specific capacitance of 273.8 F g-1 at a current density of 0.5 A g-1. More importantly, the assembled NHPCS-2-8-based symmetric capacitor displayed a high energy density of 17.2 Wh kg-1 at a power density of 178.9 W kg-1 within a voltage window of 0 ∼ 1.8 V in 0.5 M Na2SO4 aqueous electrolyte. In addition, the CO2 capture application of these NHPCS materials was also explored, and the optimal sample of NHPCS-0-8 with a large micropore proportion prepared at 800 °C exhibited an exceptional CO2 uptake capacity at ambient pressures of up to 4.23 mmol g-1 at 0 °C.

Carbon dioxide (CO2) sequestration in deep saline aquifers and formations: Chapter 3

Science.gov (United States)

Rosenbauer, Robert J.; Thomas, Burt

2010-01-01

Carbon dioxide (CO2) capture and sequestration in geologic media is one among many emerging strategies to reduce atmospheric emissions of anthropogenic CO2. This chapter looks at the potential of deep saline aquifers – based on their capacity and close proximity to large point sources of CO2 – as repositories for the geologic sequestration of CO2. The petrochemical characteristics which impact on the suitability of saline aquifers for CO2 sequestration and the role of coupled geochemical transport models and numerical tools in evaluating site feasibility are also examined. The full-scale commercial CO2 sequestration project at Sleipner is described together with ongoing pilot and demonstration projects.

Effects of the EU law on the climate protection. On the implementation of the European guideline on carbon capture and storage (CCS) into German legislation; Auswirkungen des EU-Rechts auf den Klimaschutz. Zur Umsetzung der europaeischen Richtlinie zu Carbon Capture and Storage (CCS) in das deutsche Recht

Energy Technology Data Exchange (ETDEWEB)

Greb, Tobias [SammlerUsinger Rechtsanwaelte, Berlin (Germany)

2014-07-01

The contribution is covering the implementation of the European guideline on climate protection and carbon capture and storage (CCS) into German legislation. The CCS technology and special critical aspects concerning the CCS technology are described. The specific legal frame includes the facilities for carbon dioxide precipitation, carbon dioxide pipelines, and carbon dioxide storage sites. The legal drafts concerning CCD are discussed including commissioning, and conflicts of interest. The long-term responsibility including transfer of responsibilities and follow-up regulations are further problems with respect to the implementation into German legislation.

A projection of energy consumption and carbon dioxide emissions in the electricity sector for Saudi Arabia: The case for carbon capture and storage and solar photovoltaics

International Nuclear Information System (INIS)

Mansouri, Noura Y.; Crookes, Roy J.; Korakianitis, Theodosios

2013-01-01

The paper examined the case study of the Saudi electricity sector and provided projections for energy use and respective carbon dioxide (CO 2 ) emissions for the period 2010–2025 with and without cleaner energy technologies. Based on two sets of 20 life cycle assessment studies for carbon capture and storage and solar photovoltaic technologies, CO 2 emission reduction rates were used for projecting future CO 2 emissions. Results showed enormous savings in CO 2 emissions, for the most likely case, year 2025 reported savings that range from 136 up to 235 MtCO 2 . Including low growth and high growth cases, these savings could range from 115 up to 468 MtCO 2 presenting such an unrivalled opportunity for Saudi Arabia. These projections were developed as a way of translating the inherent advantages that cleaner energy technologies could provide for CO 2 emissions savings. It is hoped that the results of this paper would inform energy policymaking in Saudi Arabia. - Highlights: • Electricity use in Saudi Arabia is predicted in the period 2010–2025. • Use of photovoltaic plants and carbon capture and storage are considered. • Life cycle assessment of the options is conducted. • Carbon emissions with and without the renewable energy are estimated. • The projections showcase the CO 2 emissions savings

Leakage and Seepage of CO2 from Geologic Carbon Sequestration Sites: CO2 Migration into Surface Water

International Nuclear Information System (INIS)

Oldenburg, Curt M.; Lewicki, Jennifer L.

2005-01-01

Geologic carbon sequestration is the capture of anthropogenic carbon dioxide (CO 2 ) and its storage in deep geologic formations. One of the concerns of geologic carbon sequestration is that injected CO 2 may leak out of the intended storage formation, migrate to the near-surface environment, and seep out of the ground or into surface water. In this research, we investigate the process of CO 2 leakage and seepage into saturated sediments and overlying surface water bodies such as rivers, lakes, wetlands, and continental shelf marine environments. Natural CO 2 and CH 4 fluxes are well studied and provide insight into the expected transport mechanisms and fate of seepage fluxes of similar magnitude. Also, natural CO 2 and CH 4 fluxes are pervasive in surface water environments at levels that may mask low-level carbon sequestration leakage and seepage. Extreme examples are the well known volcanic lakes in Cameroon where lake water supersaturated with respect to CO 2 overturned and degassed with lethal effects. Standard bubble formation and hydrostatics are applicable to CO 2 bubbles in surface water. Bubble-rise velocity in surface water is a function of bubble size and reaches a maximum of approximately 30 cm s -1 at a bubble radius of 0.7 mm. Bubble rise in saturated porous media below surface water is affected by surface tension and buoyancy forces, along with the solid matrix pore structure. For medium and fine grain sizes, surface tension forces dominate and gas transport tends to occur as channel flow rather than bubble flow. For coarse porous media such as gravels and coarse sand, buoyancy dominates and the maximum bubble rise velocity is predicted to be approximately 18 cm s -1 . Liquid CO 2 bubbles rise slower in water than gaseous CO 2 bubbles due to the smaller density contrast. A comparison of ebullition (i.e., bubble formation) and resulting bubble flow versus dispersive gas transport for CO 2 and CH 4 at three different seepage rates reveals that

Convenient and large-scale synthesis of nitrogen-rich hierarchical porous carbon spheres for supercapacitors and CO{sub 2} capture

Energy Technology Data Exchange (ETDEWEB)

Chang, Binbin, E-mail: binbinchang@infm.hhstu.edu.cn [Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou, Henan 450006 (China); Henan Provincial Key Laboratory of Nano-composite and Application, Zhengzhou, Henan 450006 (China); Zhang, Shouren; Yin, Hang [Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou, Henan 450006 (China); Henan Provincial Key Laboratory of Nano-composite and Application, Zhengzhou, Henan 450006 (China); Yang, Baocheng, E-mail: baochengyang@yahoo.com [Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou, Henan 450006 (China); Henan Provincial Key Laboratory of Nano-composite and Application, Zhengzhou, Henan 450006 (China)

2017-08-01

Highlights: • Convenient and large-scale synthesis route for N-doped hierarchical porous carbon sphere. • The resultant own spherical morphology, tunable hierarchical porosity, high surface area. • The optimal material exhibits a high CO{sub 2} capture capacity of 4.23 mmol g{sup −1}. • It shows a large voltage window of 1.8 V for symmetric cell in 0.5 M Na{sub 2}SO{sub 4}. - Abstract: Herein, considering the great potential of nitrogen-doped hierarchical porous carbons in energy storage and CO{sub 2} capture, we designed a convenient and easily large-scale production strategy for preparing nitrogen-doped hierarchical porous carbon sphere (NHPCS) materials. In this synthesis route, spherical resorcinol-formaldehyde (RF) resins were selected as carbon precursor, and then the ZnCl{sub 2}-impregnated RF resin spheres were carbonized in a NH{sub 3} atmosphere at a temperature range of 600–800 °C. During the one-step heat-treatment process, nitrogen atom could be efficiently incorporated into the carbon skeleton, and the interconnected and hierarchical pore structure with different micro/mesopore proportion could be generated and tuned by adjusting the activating agent ZnCl{sub 2} dosage and carbonization temperature. The resultant nitrogen-doped hierarchical porous carbon sphere materials exhibited a satisfactory charge storage capacity, and the optimal sample of NHPCS-2-8 with a high mesopore proportion obtained at 800 °C with a ZnCl{sub 2}/RF mass ratio of 2:1 presented a specific capacitance of 273.8 F g{sup −1} at a current density of 0.5 A g{sup −1}. More importantly, the assembled NHPCS-2-8-based symmetric capacitor displayed a high energy density of 17.2 Wh kg{sup −1} at a power density of 178.9 W kg{sup −1} within a voltage window of 0 ∼ 1.8 V in 0.5 M Na{sub 2}SO{sub 4} aqueous electrolyte. In addition, the CO{sub 2} capture application of these NHPCS materials was also explored, and the optimal sample of NHPCS-0-8 with a large

Atmospheric chemistry and environmental impact of the use of amines in carbon capture and storage (CCS).

Science.gov (United States)

Nielsen, Claus J; Herrmann, Hartmut; Weller, Christian

2012-10-07

This critical review addresses the atmospheric gas phase and aqueous phase amine chemistry that is relevant to potential emissions from amine-based carbon capture and storage (CCS). The focus is on amine, nitrosamine and nitramine degradation, and nitrosamine and nitramine formation processes. A comparison between the relative importance of the various atmospheric sinks for amines, nitrosamines and nitramines is presented.

Clayey cap-rocks reactivity in presence of CO2 in deep geological storage conditions: experimentation/modeling integrated approach

International Nuclear Information System (INIS)

Credoz, A.

2009-10-01

CO 2 capture, transport and geological storage is one of the main solutions considered in the short and medium term to reduce CO 2 and others greenhouse gases emissions towards the atmosphere, by storing CO 2 in deeper geological reservoirs during 100 to 10 000 years. This Ph-D study offers a multi-scale vision of complex clayey cap-rocks reactivity and evolution. These formations are identified for the CO 2 containment and sealing into the reservoir. From the experimental scale on purified clay minerals to integrative modeling at high space and time scales, the strategy developed allowed identifying the main geochemical processes, to check the good agreement between experiment and modeling, and to lay emphasis the operational impacts on long-term cap-rocks integrity. Carbonated cements alteration is likely to open cap-rock porosity and to create preferential reactive pathway for reactive fluid flow. Besides, this could alter the cap-rock structure and the global geo-mechanic properties. Clay minerals alteration, including the illitization process, reduces the clay fraction volume but considerably limits the porosity increase. The illitization process in acidic conditions determined experimentally and by modeling at low and high scale, is coupled with silica precipitation. The final porosity increase control results of these two reactive processes balance. By a fundamental side, this study reveals new kinetic parameters of clay minerals and highlights new structural transformations. By an operational side, this study contributes to the acquisition of qualitative data (long-term reactive pathways of clayey cap-rocks, coupled reactivity carbonates/clays) and quantitative data (CO 2 penetration distance into the cap-rock) to partly answer to the performance and safety assessment CO 2 capture and geological storage. (author)

Microporous polystyrene particles for selective carbon dioxide capture.

Science.gov (United States)

Kaliva, Maria; Armatas, Gerasimos S; Vamvakaki, Maria

2012-02-07

This study presents the synthesis of microporous polystyrene particles and the potential use of these materials in CO(2) capture for biogas purification. Highly cross-linked polystyrene particles are synthesized by the emulsion copolymerization of styrene (St) and divinylbenzene (DVB) in water. The cross-link density of the polymer is varied by altering the St/DVB molar ratio. The size and the morphology of the particles are characterized by scanning and transmission electron microscopy. Following supercritical point drying with carbon dioxide or lyophilization from benzene, the polystyrene nanoparticles exhibit a significant surface area and permanent microporosity. The dried particles comprising 35 mol % St and 65 mol % DVB possess the largest surface area, ∼205 m(2)/g measured by Brunauer-Emmett-Teller and ∼185 m(2)/g measured by the Dubinin-Radushkevich method, and a total pore volume of 1.10 cm(3)/g. Low pressure measurements suggest that the microporous polystyrene particles exhibit a good separation performance of CO(2) over CH(4), with separation factors in the range of ∼7-13 (268 K, CO(2)/CH(4) = 5/95 gas mixture), which renders them attractive candidates for use in gas separation processes.

Superior capture of CO2 achieved by introducing extra-framework cations into N-doped microporous carbon

KAUST Repository

Zhao, Yunfeng

2012-12-21

We designed and prepared a novel microporous carbon material (KNC-A-K) for selective CO2 capture. The combination of a high N-doping concentration (>10 wt %) and extra-framework cations, which were introduced into carbonaceous sorbents for the first time, endowed KNC-A-K with exceptional CO2 adsorption capabilities, especially at low pressures. Specifically, KNC-A-K exhibited CO2 uptake of 1.62 mmol g -1 at 25 C and 0.1 bar, far exceeding the CO2 adsorption capability of most reported carbon material to date. Single component adsorption isotherms indicated that its CO2/N2 selectivity was 48, which also significantly surpasses the selectivity of conventional carbon materials. Furthermore, breakthrough experiments were conducted to evaluate the CO2 separation capability of KNC-A-K on CO2/N2 (10:90 v/v) mixtures under kinetic flow conditions, and the obtained CO 2/N2 selectivity was as high as 44, comparable to that predicted from equilibrium adsorption data. Upon facile regeneration, KNC-A-K showed constant CO2 adsorption capacity and selectivity during multiple mixed-gas separation cycles. Its outstanding low-pressure CO 2 adsorption ability makes KNC-A-K a promising candidate for selective CO2 capture from flue gas. Theoretical calculations indicated that K+ ions play a key role in promoting CO2 adsorption via electrostatic interactions. In addition, we found that HCl molecules anchored in N-doped carbon have a similar promotion effect on CO 2 adsorption, which contradicts the conventional wisdom that the neutralization of basic sites by acids diminishes the adsorption of acidic CO2 gas. © 2012 American Chemical Society.

Cauliflower-derived porous carbon without activation for electrochemical capacitor and CO2 capture applications

Science.gov (United States)

Du, Juan; Yu, Yifeng; Lv, Haijun; Chen, Chunlin; Zhang, Jian; Chen, Aibing

2018-01-01

Carbon materials have attracted great attention in CO2 capture and energy storage due to their excellent characteristics such as tunable pore structure, modulated surface properties and superior bulk conductivities, etc. Biomass, provided by nature with non-toxic, widespread, abundant, and sustainable advantages, is considered to be a very promising precursor of carbons for the view of economic, environmental, and societal issues. However, the preparation of high-performance biomass-derived carbons is still a big challenge because of the multistep process for their synthesis and subsequent activation. Herein, hierarchically porous structured carbon materials have been prepared by directly carbonizing dried cauliflowers without any addition of agents and activation process, featuring with large specific surface area, hierarchically porous structure and improved pore volume, as well as suitable nitrogen content. Being used as a solid-state CO2 adsorbent, the obtained product exhibited a high CO2 adsorption capacity of 3.1 mmol g-1 under 1 bar and 25 °C and a remarkable reusability of 96.7% retention after 20 adsorption/regeneration cycles. Our study reveals that choosing a good biomass source was significant as the unique structure of precursor endows the carbonized product with abundant pores without the need of any post-treatment. Used as an electrode material in electrochemical capacitor, the non-activated porous carbon displayed a fairly high specific capacitance of 228.9 F g-1 at 0.5 A g-1 and an outstanding stability of 99.2% retention after 5000 cycles at 5 A g-1. [Figure not available: see fulltext.

Novel Silica Nanostructured Platforms with Engineered Surface Functionality and Spherical Morphology for Low-Cost High-Efficiency Carbon Capture

Energy Technology Data Exchange (ETDEWEB)

Lai, Cheng-Yu [Delaware State Univ., Dover, DE (United States); Radu, Daniela [Delaware State Univ., Dover, DE (United States); Univ. of Delaware, Newark, DE (United States)

2017-12-29

Carbon capture is an integral part of the CO₂ mitigation efforts, and encompasses, among other measures, the demonstration of effective and inexpensive CO₂ capture technologies. The project demonstrated a novel platform—the amine-functionalized stellate mesoporous silica nanosphere (MSN)—for effective CO₂ absorption. The reported CO₂ absorption data are superior to the performance of other reported silica matrices utilized for carbon capture, featuring an amount of over 4 milimoles CO₂/g sorbent at low temperatures (in the range of 30-45 ºC), selected for simulating the temperature of actual flue gas. The reported platform is highly resilient, showing recyclability and 85 % mass conservation of sorbent upon nine tested cycles. Importantly, the stellate MSNs show high CO₂ selectivity at room temperature, indicating that the presence of nitrogen in flue gas will not impair the CO₂ absorption performance. The results could lead to a simple and inexpensive new technology for CO₂ mitigation which could be implemented as measure of CO₂ mitigation in current fossil-fuel burning plants in the form of solid sorbent.

Carbon dioxide utilization in a microalga-based biorefinery: Efficiency of carbon removal and economic performance under carbon taxation.

Science.gov (United States)

Wiesberg, Igor Lapenda; Brigagão, George Victor; de Medeiros, José Luiz; de Queiroz Fernandes Araújo, Ofélia

2017-12-01

Coal-fired power plants are major stationary sources of carbon dioxide and environmental constraints demand technologies for abatement. Although Carbon Capture and Storage is the most mature route, it poses severe economic penalty to power generation. Alternatively, this penalty is potentially reduced by Carbon Capture and Utilization, which converts carbon dioxide to valuable products, monetizing it. This work evaluates a route consisting of carbon dioxide bio-capture by Chlorella pyrenoidosa and use of the resulting biomass as feedstock to a microalgae-based biorefinery; Carbon Capture and Storage route is evaluated as a reference technology. The integrated arrangement comprises: (a) carbon dioxide biocapture in a photobioreactor, (b) oil extraction from part of the produced biomass, (b) gasification of remaining biomass to obtain bio-syngas, and (c) conversion of bio-syngas to methanol. Calculation of capital and operational expenditures are estimated based on mass and energy balances obtained by process simulation for both routes (Carbon Capture and Storage and the biorefinery). Capital expenditure for the biorefinery is higher by a factor of 6.7, while operational expenditure is lower by a factor of 0.45 and revenues occur only for this route, with a ratio revenue/operational expenditure of 1.6. The photobioreactor is responsible for one fifth of the biorefinery capital expenditure, with footprint of about 1000 ha, posing the most significant barrier for technical and economic feasibility of the proposed biorefinery. The Biorefinery and Carbon Capture and Storage routes show carbon dioxide capture efficiency of 73% and 48%, respectively, with capture cost of 139$/t and 304$/t. Additionally, the biorefinery has superior performance in all evaluated metrics of environmental impacts. Copyright © 2017 Elsevier Ltd. All rights reserved.

Technology and demand forecasting for carbon capture and storage technology in South Korea

International Nuclear Information System (INIS)

Shin, Jungwoo; Lee, Chul-Yong; Kim, Hongbum

2016-01-01

Among the various alternatives available to reduce greenhouse gas (GHG) emissions, carbon capture and storage (CCS) is considered to be a prospective technology that could both improve economic growth and meet GHG emission reduction targets. Despite the importance of CCS, however, studies of technology and demand forecasting for CCS are scarce. This study bridges this gap in the body of knowledge on this topic by forecasting CCS technology and demand based on an integrated model. For technology forecasting, a logistic model and patent network analysis are used to compare the competitiveness of CCS technology for selected countries. For demand forecasting, a competition diffusion model is adopted to consider competition among renewable energies and forecast demand. The results show that the number of patent applications for CCS technology will increase to 16,156 worldwide and to 4,790 in Korea by 2025. We also find that the United States has the most competitive CCS technology followed by Korea and France. Moreover, about 5 million tCO_2e of GHG will be reduced by 2040 if CCS technology is adopted in Korea after 2020. - Highlights: • Carbon capture and storage (CCS) can help mitigate climate change globally. • It can both improve economic growth and meet GHG emission reduction targets. • We forecast CCS technology and demand based on an integrated model. • The US has the most competitive CCS technology followed by Korea and France. • 5 million tCO_2e of GHG will be reduced by 2040 if CCS is adopted in Korea.

Review of carbon dioxide capture and storage with relevance to the South African power sector

Directory of Open Access Journals (Sweden)

Khalid Osman

2014-05-01

Full Text Available Carbon dioxide (CO2 emissions and their association with climate change are currently a major discussion point in government and amongst the public at large in South Africa, especially because of the country's heavy reliance on fossil fuels for electricity production. Here we review the current situation regarding CO2 emissions in the South African power generation sector, and potential process engineering solutions to reduce these emissions. Estimates of CO2 emissions are presented, with the main sources of emissions identified and benchmarked to other countries. A promising mid-term solution for mitigation of high CO2 emissions, known as CO2 capture and storage, is reviewed. The various aspects of CO2 capture and storage technology and techniques for CO2 capture from pulverised coal power plants are discussed; these techniques include processes such as gas absorption, hydrate formation, cryogenic separation, membrane usage, sorbent usage, enzyme-based systems and metal organic frameworks. The latest power plant designs which optimise CO2 capture are also discussed and include integrated gasification combined cycle, oxy-fuel combustion, integrated gasification steam cycle and chemical looping combustion. Each CO2 capture technique and plant modification is presented in terms of the conceptual idea, the advantages and disadvantages, and the extent of development and applicability in a South African context. Lastly, CO2 transportation, storage, and potential uses are also presented. The main conclusions of this review are that gas absorption using solvents is currently most applicable for CO2 capture and that enhanced coal bed methane recovery could provide the best disposal route for CO2 emissions mitigation in South Africa.

The global carbon nation: Status of CO2 capture, storage and utilization

Science.gov (United States)

Kocs, Elizabeth A.

2017-07-01

As the world transitions toward cleaner and more sustainable energy generation, Carbon Capture and Sequestration/Storage (CCS) plays an essential role in the portfolio of technologies to help reduce global greenhouse gas (GHG) emissions. The projected increase in population size and its resulting increase in global energy consumption, for both transportation and the electricity grid —the largest emitters of greenhouse gases, will continue to add to current CO2 emissions levels during this transition. Since eighty percent of today's global energy continues to be generated by fossil fuels, a shift to low-carbon energy sources will take many decades. In recent years, shifting to renewables and increasing energy efficiencies have taken more importance than deploying CCS. Together, this triad —renewables, energy efficiency, and CCS— represent a strong paradigm for achieving a carbon-free world. Additionally, the need to accelerate CCS in developing economies like China and India are of increasing concern since migration to renewables is unlikely to occur quickly in those countries. CCS of stationary sources, accounting for only 20% reduction in emissions, as well as increasing efficiency in current systems are needed for major reductions in emissions. A rising urgency for fifty to eighty percent reduction of CO2 emissions by 2050 and one hundred percent reduction by 2100 makes CCS all that more critical in the transition to a cleaner-energy future globally.

Identification and Selection of Major Carbon Dioxide Stream Compositions

Energy Technology Data Exchange (ETDEWEB)

Last, George V.; Schmick, Mary T.

2011-06-30

A critical component in the assessment of long-term risk from geologic sequestration of CO2 is the ability to predict mineralogical and geochemical changes within storage reservoirs due to rock-brine-CO2 reactions. Impurities and/or other constituents selected for co-sequestration can affect both the chemical and physical (e.g. density, viscosity, interfacial tension) behavior of CO2 in the deep subsurface. These impurities and concentrations are a function of both the industrial source(s) of the CO2, as well as the carbon capture technology used to extract the CO2 and produce a concentrated stream for geologic sequestration. This report summarizes the relative concentrations of CO2 and other constituents in exhaust gases from major non-energy related industrial sources of CO2. Assuming that carbon-capture technology would remove most of the incondensable gases N2, O2, and Ar, leaving SO2 and NOx as the main impurities, we selected four test fluid compositions for use in geochemical experiments. These included: 1) a pure CO2 stream representative of food grade CO2 used in most enhanced oil recovery projects: 2) a test fluid composition containing low concentrations (0.5 mole %) SO2 and NOx (representative of that generated from cement production), 3) a test fluid composition with higher concentrations (2.5 mole %) of SO2, and 4) and test fluid composition containing 3 mole % H2S.

Dynamic Operation and Simulation of Post-Combustion CO2 Capture

DEFF Research Database (Denmark)

Gaspar, Jozsef; Gladis, Arne; Jørgensen, John Bagterp

2016-01-01

Thermal power need to operate, on a daily basis, with frequent and fast load changes to balance the large variations of intermittent energy sources, such as wind and solar energy. To make the integration of carbon capture to power plants economically and technically feasible, the carbon capture...... process has to be able to follow these fast and large load changes without decreasing the overall performance of the carbon capture plant. Therefore, dynamic models for simulation, optimization and control system design are essential. In this work, we compare the transient behavior of the model against...

Silica-coated multi-walled carbon nanotubes impregnated with polyethyleneimine for carbon dioxide capture under the flue gas condition

Energy Technology Data Exchange (ETDEWEB)

Lee, Min-Sang; Park, Soo-Jin, E-mail: sjpark@inha.ac.kr

2015-03-15

In this study, silica-coated multi-walled carbon nanotubes impregnated with polyethyleneimine (PEI) were prepared via a two-step process: (i) hydrolysis of tetraethylorthosilicate onto multi-walled carbon nanotubes, and (ii) impregnation of PEI. The adsorption properties of CO{sub 2} were investigated using CO{sub 2} adsorption–desorption isotherms at 298 K and thermogravimetric analysis under the flue gas condition (15% CO{sub 2}/85% N{sub 2}). The results obtained in this study indicate that CO{sub 2} adsorption increases after impregnation of PEI. The increase in CO{sub 2} capture was attributed to the affinity between CO{sub 2} and the amine groups. CO{sub 2} adsorption–desorption experiments, which were repeated five times, also showed that the prepared adsorbents have excellent regeneration properties. - Graphical abstract: Fabrication and CO{sub 2} adsorption process of the S-MWCNTs impregnated with PEI. - Highlights: • Silica coated-MWCNT impregnated with PEI was synthesized. • Amine groups of PEI gave CO{sub 2} affinity sites on MWCNT surfaces. • The S-MWCNT/PEI(50) exhibited the highest CO{sub 2} adsorption capacity.

THE INTERMEDIATE NEUTRON-CAPTURE PROCESS AND CARBON-ENHANCED METAL-POOR STARS

Energy Technology Data Exchange (ETDEWEB)

Hampel, Melanie [Zentrum für Astronomie der Universität Heidelberg, Landessternwarte, Königstuhl 12, D-69117 Heidelberg (Germany); Stancliffe, Richard J. [Argelander-Institut für Astronomie, University of Bonn, Auf dem Hügel 71, D-53121 Bonn (Germany); Lugaro, Maria [Konkoly Observatory, Research Centre for Astronomy and Earth Sciences, Hungarian Academy of Sciences, H-1121 Budapest (Hungary); Meyer, Bradley S., E-mail: mhampel@lsw.uni-heidelberg.de [Department of Physics and Astronomy, Clemson University, Clemson, SC 29634-0978 (United States)

2016-11-10

Carbon-enhanced metal-poor (CEMP) stars in the Galactic Halo display enrichments in heavy elements associated with either the s (slow) or the r (rapid) neutron-capture process (e.g., barium and europium, respectively), and in some cases they display evidence of both. The abundance patterns of these CEMP- s / r stars, which show both Ba and Eu enrichment, are particularly puzzling, since the s and the r processes require neutron densities that are more than ten orders of magnitude apart and, hence, are thought to occur in very different stellar sites with very different physical conditions. We investigate whether the abundance patterns of CEMP- s / r stars can arise from the nucleosynthesis of the intermediate neutron-capture process (the i process), which is characterized by neutron densities between those of the s and the r processes. Using nuclear network calculations, we study neutron capture nucleosynthesis at different constant neutron densities n ranging from 10{sup 7}–10{sup 15} cm{sup -3}. With respect to the classical s process resulting from neutron densities on the lowest side of this range, neutron densities on the highest side result in abundance patterns, which show an increased production of heavy s -process and r -process elements, but similar abundances of the light s -process elements. Such high values of n may occur in the thermal pulses of asymptotic giant branch stars due to proton ingestion episodes. Comparison to the surface abundances of 20 CEMP- s / r stars shows that our modeled i -process abundances successfully reproduce observed abundance patterns, which could not be previously explained by s -process nucleosynthesis. Because the i -process models fit the abundances of CEMP- s / r stars so well, we propose that this class should be renamed as CEMP- i .