CO2 Accounting and Risk Analysis for CO2 Sequestration at Enhanced Oil Recovery Sites.

Science.gov (United States)

Dai, Zhenxue; Viswanathan, Hari; Middleton, Richard; Pan, Feng; Ampomah, William; Yang, Changbing; Jia, Wei; Xiao, Ting; Lee, Si-Yong; McPherson, Brian; Balch, Robert; Grigg, Reid; White, Mark

2016-07-19

Using CO2 in enhanced oil recovery (CO2-EOR) is a promising technology for emissions management because CO2-EOR can dramatically reduce sequestration costs in the absence of emissions policies that include incentives for carbon capture and storage. This study develops a multiscale statistical framework to perform CO2 accounting and risk analysis in an EOR environment at the Farnsworth Unit (FWU), Texas. A set of geostatistical-based Monte Carlo simulations of CO2-oil/gas-water flow and transport in the Morrow formation are conducted for global sensitivity and statistical analysis of the major risk metrics: CO2/water injection/production rates, cumulative net CO2 storage, cumulative oil/gas productions, and CO2 breakthrough time. The median and confidence intervals are estimated for quantifying uncertainty ranges of the risk metrics. A response-surface-based economic model has been derived to calculate the CO2-EOR profitability for the FWU site with a current oil price, which suggests that approximately 31% of the 1000 realizations can be profitable. If government carbon-tax credits are available, or the oil price goes up or CO2 capture and operating expenses reduce, more realizations would be profitable. The results from this study provide valuable insights for understanding CO2 storage potential and the corresponding environmental and economic risks of commercial-scale CO2-sequestration in depleted reservoirs.

ECONOMIC EVALUATION OF CO2 SEQUESTRATION TECHNOLOGIES

Energy Technology Data Exchange (ETDEWEB)

Bert R. Bock; Richard G. Rhudy; David E. Nichols

2001-07-01

In order to plan for potential CO{sub 2} mitigation mandates, utilities need better information on CO{sub 2} mitigation options, especially carbon sequestration options that involve non-utility operations. One of the major difficulties in evaluating CO{sub 2} sequestration technologies and practices, both geologic storage of captured CO{sub 2} and storage in biological sinks, is obtaining consistent, transparent, accurate, and comparable economics. This project is comparing the economics of major technologies and practices under development for CO{sub 2} sequestration, including captured CO{sub 2} storage options such as active oil reservoirs, depleted oil and gas reservoirs, deep aquifers, coal beds, and oceans, as well as the enhancement of biological sinks such as forests and croplands. An international group of experts has been assembled to compare on a consistent basis the economics of this diverse array of CO{sub 2} sequestration options. Designs and data collection are nearly complete for each of the CO{sub 2} sequestration options being compared. Initial spreadsheet development has begun on concepts involving storage of captured CO{sub 2}. No significant problems have been encountered, but some additional outside expertise will be accessed to supplement the team's expertise in the areas of life cycle analysis, oil and gas exploration and production, and comparing CO{sub 2} sequestration options that differ in timing and permanence of CO{sub 2} sequestration. Plans for the next reporting period are to complete data collection and a first approximation of the spreadsheet. We expect to complete this project on time and on budget.

Enhanced Coal Bed Methane Recovery and CO2 Sequestration in the Powder River Basin

Energy Technology Data Exchange (ETDEWEB)

Eric P. Robertson

2010-06-01

Unminable coal beds are potentially large storage reservoirs for the sequestration of anthropogenic CO2 and offer the benefit of enhanced methane production, which can offset some of the costs associated with CO2 sequestration. The objective of this report is to provide a final topical report on enhanced coal bed methane recovery and CO2 sequestration to the U.S. Department of Energy in fulfillment of a Big Sky Carbon Sequestration Partnership milestone. This report summarizes work done at Idaho National Laboratory in support of Phase II of the Big Sky Carbon Sequestration Partnership. Research that elucidates the interaction of CO2 and coal is discussed with work centering on the Powder River Basin of Wyoming and Montana. Sorption-induced strain, also referred to as coal swelling/shrinkage, was investigated. A new method of obtaining sorption-induced strain was developed that greatly decreases the time necessary for data collection and increases the reliability of the strain data. As coal permeability is a strong function of sorption-induced strain, common permeability models were used to fit measured permeability data, but were found inadequate. A new permeability model was developed that can be directly applied to coal permeability data obtained under laboratory stress conditions, which are different than field stress conditions. The coal permeability model can be used to obtain critical coal parameters that can be applied in field models. An economic feasibility study of CO2 sequestration in unminable coal seams in the Powder River Basin of Wyoming was done. Economic analyses of CO2 injection options are compared. Results show that injecting flue gas to recover methane from CBM fields is marginally economical; however, this method will not significantly contribute to the need to sequester large quantities of CO2. Separating CO2 from flue gas and injecting it into the unminable coal zones of the Powder River Basin seam is currently uneconomical, but can

Microbial electrolysis desalination and chemical-production cell for CO2 sequestration

KAUST Repository

Zhu, Xiuping

2014-05-01

Mineral carbonation can be used for CO2 sequestration, but the reaction rate is slow. In order to accelerate mineral carbonation, acid generated in a microbial electrolysis desalination and chemical-production cell (MEDCC) was examined to dissolve natural minerals rich in magnesium/calcium silicates (serpentine), and the alkali generated by the same process was used to absorb CO2 and precipitate magnesium/calcium carbonates. The concentrations of Mg2+ and Ca2+ dissolved from serpentine increased 20 and 145 times by using the acid solution. Under optimal conditions, 24mg of CO2 was absorbed into the alkaline solution and 13mg of CO2 was precipitated as magnesium/calcium carbonates over a fed-batch cycle (24h). Additionally, the MEDCC removed 94% of the COD (initially 822mg/L) and achieved 22% desalination (initially 35g/L NaCl). These results demonstrate the viability of this process for effective CO2 sequestration using renewable organic matter and natural minerals. © 2014 Elsevier Ltd.

Calcium silicates synthesised from industrial residues with the ability for CO2 sequestration.

Science.gov (United States)

Morales-Flórez, Victor; Santos, Alberto; López, Antonio; Moriña, Isabel; Esquivias, Luis

2014-12-01

This work explored several synthesis routes to obtain calcium silicates from different calcium-rich and silica-rich industrial residues. Larnite, wollastonite and calcium silicate chloride were successfully synthesised with moderate heat treatments below standard temperatures. These procedures help to not only conserve natural resources, but also to reduce the energy requirements and CO2 emissions. In addition, these silicates have been successfully tested as carbon dioxide sequesters, to enhance the viability of CO2 mineral sequestration technologies using calcium-rich industrial by-products as sequestration agents. Two different carbon sequestration experiments were performed under ambient conditions. Static experiments revealed carbonation efficiencies close to 100% and real-time resolved experiments characterised the dynamic behaviour and ability of these samples to reduce the CO2 concentration within a mixture of gases. The CO2 concentration was reduced up to 70%, with a carbon fixation dynamic ratio of 3.2 mg CO2 per g of sequestration agent and minute. Our results confirm the suitability of the proposed synthesis routes to synthesise different calcium silicates recycling industrial residues, being therefore energetically more efficient and environmentally friendly procedures for the cement industry. © The Author(s) 2014.

Analysis of ex situ processes of CO2 sequestration. Final report

International Nuclear Information System (INIS)

Touze, S.; Bourgeois, F.; Baranger, P.; Durst, P.

2004-01-01

The aim of this study is to bring quantitative elements to evaluate the validation of the CO 2 mineral sequestration to limit the greenhouse effect gases. This analysis aims to calculate the CO 2 accounting of the system (internal energy production balance the energy expend) sequestrated CO 2 and produced CO 2 . The first part detailed the possible experimental solutions. Then two carbonation processes, direct and indirect, have been chosen of the analysis. (A.L.B.)

ECONOMIC EVALUATION OF CO2 SEQUESTRATION TECHNOLOGIES; SEMIANNUAL

International Nuclear Information System (INIS)

Bert R. Bock; Richard G. Rhudy; David E. Nichols

2001-01-01

In order to plan for potential CO(sub 2) mitigation mandates, utilities need better information on CO(sub 2) mitigation options, especially carbon sequestration options that involve non-utility operations. One of the major difficulties in evaluating CO(sub 2) sequestration technologies and practices, both geologic storage of captured CO(sub 2) and storage in biological sinks, is obtaining consistent, transparent, accurate, and comparable economics. This project is comparing the economics of major technologies and practices under development for CO(sub 2) sequestration, including captured CO(sub 2) storage options such as active oil reservoirs, depleted oil and gas reservoirs, deep aquifers, coal beds, and oceans, as well as the enhancement of biological sinks such as forests and croplands. An international group of experts has been assembled to compare on a consistent basis the economics of this diverse array of CO(sub 2) sequestration options. Designs and data collection are nearly complete for each of the CO(sub 2) sequestration options being compared. Initial spreadsheet development has begun on concepts involving storage of captured CO(sub 2). No significant problems have been encountered, but some additional outside expertise will be accessed to supplement the team's expertise in the areas of life cycle analysis, oil and gas exploration and production, and comparing CO(sub 2) sequestration options that differ in timing and permanence of CO(sub 2) sequestration. Plans for the next reporting period are to complete data collection and a first approximation of the spreadsheet. We expect to complete this project on time and on budget

Thermodynamic Data for Geochemical Modeling of Carbonate Reactions Associated with CO2 Sequestration - Literature Review

International Nuclear Information System (INIS)

Krupka, Kenneth M.; Cantrell, Kirk J.; McGrail, B. Peter

2010-01-01

Permanent storage of anthropogenic CO 2 in deep geologic formations is being considered as a means to reduce the concentration of atmospheric CO 2 and thus its contribution to global climate change. To ensure safe and effective geologic sequestration, numerous studies have been completed of the extent to which the CO 2 migrates within geologic formations and what physical and geochemical changes occur in these formations when CO 2 is injected. Sophisticated, computerized reservoir simulations are used as part of field site and laboratory CO 2 sequestration studies. These simulations use coupled multiphase flow-reactive chemical transport models and/or standalone (i.e., no coupled fluid transport) geochemical models to calculate gas solubility, aqueous complexation, reduction/oxidation (redox), and/or mineral solubility reactions related to CO 2 injection and sequestration. Thermodynamic data are critical inputs to modeling geochemical processes. The adequacy of thermodynamic data for carbonate compounds has been identified as an important data requirement for the successful application of these geochemical reaction models to CO 2 sequestration. A review of thermodynamic data for CO 2 gas and carbonate aqueous species and minerals present in published data compilations and databases used in geochemical reaction models was therefore completed. Published studies that describe mineralogical analyses from CO 2 sequestration field and natural analogue sites and laboratory studies were also reviewed to identify specific carbonate minerals that are important to CO 2 sequestration reactions and therefore require thermodynamic data. The results of the literature review indicated that an extensive thermodynamic database exists for CO 2 and CH 4 gases, carbonate aqueous species, and carbonate minerals. Values of Δ f G 298 o and/or log K r,298 o are available for essentially all of these compounds. However, log K r,T o or heat capacity values at temperatures above 298 K exist

Carbon dioxide sequestration by mineral carbonation

NARCIS (Netherlands)

Huijgen, W.J.J.

2007-01-01

The increasing atmospheric carbon dioxide (CO2) concentration, mainly caused by fossil fuel combustion, has lead to concerns about global warming. A possible technology that can contribute to the reduction of carbon dioxide emissions is CO2 sequestration by mineral carbonation. The basic concept

Microbial electrolysis desalination and chemical-production cell for CO2 sequestration

KAUST Repository

Zhu, Xiuping; Logan, Bruce E.

2014-01-01

Mineral carbonation can be used for CO2 sequestration, but the reaction rate is slow. In order to accelerate mineral carbonation, acid generated in a microbial electrolysis desalination and chemical-production cell (MEDCC) was examined to dissolve

Thermodynamic Data for Geochemical Modeling of Carbonate Reactions Associated with CO2 Sequestration – Literature Review

Energy Technology Data Exchange (ETDEWEB)

Krupka, Kenneth M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Cantrell, Kirk J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McGrail, B. Peter [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2010-09-01

Permanent storage of anthropogenic CO2 in deep geologic formations is being considered as a means to reduce the concentration of atmospheric CO2 and thus its contribution to global climate change. To ensure safe and effective geologic sequestration, numerous studies have been completed of the extent to which the CO2 migrates within geologic formations and what physical and geochemical changes occur in these formations when CO2 is injected. Sophisticated, computerized reservoir simulations are used as part of field site and laboratory CO2 sequestration studies. These simulations use coupled multiphase flow-reactive chemical transport models and/or standalone (i.e., no coupled fluid transport) geochemical models to calculate gas solubility, aqueous complexation, reduction/oxidation (redox), and/or mineral solubility reactions related to CO2 injection and sequestration. Thermodynamic data are critical inputs to modeling geochemical processes. The adequacy of thermodynamic data for carbonate compounds has been identified as an important data requirement for the successful application of these geochemical reaction models to CO2 sequestration. A review of thermodynamic data for CO2 gas and carbonate aqueous species and minerals present in published data compilations and databases used in geochemical reaction models was therefore completed. Published studies that describe mineralogical analyses from CO2 sequestration field and natural analogue sites and laboratory studies were also reviewed to identify specific carbonate minerals that are important to CO2 sequestration reactions and therefore require thermodynamic data. The results of the literature review indicated that an extensive thermodynamic database exists for CO2 and CH4 gases, carbonate aqueous species, and carbonate minerals. Values of ΔfG298° and/or log Kr,298° are available for essentially all of these compounds. However, log Kr,T° or heat capacity values at temperatures above 298 K exist for less than

Predictive modeling of CO2 sequestration in deep saline sandstone reservoirs: Impacts of geochemical kinetics

Energy Technology Data Exchange (ETDEWEB)

Balashov, Victor N.; Guthrie, George D.; Hakala, J. Alexandra; Lopano, Christina L.; Rimstidt, J. Donald; Brantley, Susan L.

2013-03-01

One idea for mitigating the increase in fossil-fuel generated CO{sub 2} in the atmosphere is to inject CO{sub 2} into subsurface saline sandstone reservoirs. To decide whether to try such sequestration at a globally significant scale will require the ability to predict the fate of injected CO{sub 2}. Thus, models are needed to predict the rates and extents of subsurface rock-water-gas interactions. Several reactive transport models for CO{sub 2} sequestration created in the last decade predicted sequestration in sandstone reservoirs of ~17 to ~90 kg CO{sub 2} m{sup -3|. To build confidence in such models, a baseline problem including rock + water chemistry is proposed as the basis for future modeling so that both the models and the parameterizations can be compared systematically. In addition, a reactive diffusion model is used to investigate the fate of injected supercritical CO{sub 2} fluid in the proposed baseline reservoir + brine system. In the baseline problem, injected CO{sub 2} is redistributed from the supercritical (SC) free phase by dissolution into pore brine and by formation of carbonates in the sandstone. The numerical transport model incorporates a full kinetic description of mineral-water reactions under the assumption that transport is by diffusion only. Sensitivity tests were also run to understand which mineral kinetics reactions are important for CO{sub 2} trapping. The diffusion transport model shows that for the first ~20 years after CO{sub 2} diffusion initiates, CO{sub 2} is mostly consumed by dissolution into the brine to form CO{sub 2,aq} (solubility trapping). From 20-200 years, both solubility and mineral trapping are important as calcite precipitation is driven by dissolution of oligoclase. From 200 to 1000 years, mineral trapping is the most important sequestration mechanism, as smectite dissolves and calcite precipitates. Beyond 2000 years, most trapping is due to formation of aqueous HCO{sub 3}{sup -}. Ninety-seven percent of the

Procedure to use phosphogypsum industrial waste for mineral CO2 sequestration

International Nuclear Information System (INIS)

Cárdenas-Escudero, C.; Morales-Flórez, V.; Pérez-López, R.; Santos, A.; Esquivias, L.

2011-01-01

Highlights: ► Phosphogypsum wastes are proposed to reduce CO 2 greenhouse gas emissions. ► Phosphogypsum dissolution with NaOH results in Ca(OH) 2 precipitation and Na 2 SO 4 . ► Aqueous carbonation of Ca(OH) 2 with CO 2 results in the CaCO 3 precipitation. ► Metals contained in the phosphogypsum are transferred to the final calcite. ► Applications of CaCO 3 and Na 2 SiO 4 by-products are proposed to improve viability. - Abstract: Industrial wet phosphoric acid production in Huelva (SW Spain) has led to the controversial stockpiling of waste phosphogypsum by-products, resulting in the release of significant quantities of toxic impurities in salt marshes in the Tinto river estuary. In the framework of the fight against global climate change and the effort to reduce carbon dioxide emissions, a simple and efficient procedure for CO 2 mineral sequestration is presented in this work, using phosphogypsum waste as a calcium source. Our results demonstrate the high efficiency of portlandite precipitation by phosphogypsum dissolution using an alkaline soda solution. Carbonation experiments performed at ambient pressure and temperature resulted in total conversion of the portlandite into carbonate. The fate of trace elements present in the phosphogypsum waste was also investigated, and trace impurities were found to be completely transferred to the final calcite. We believe that the procedure proposed here should be considered not only as a solution for reducing old stockpiles of phosphogypsum wastes, but also for future phosphoric acid and other gypsum-producing industrial processes, resulting in more sustainable production.

ATOMIC-LEVEL IMAGING OF CO2 DISPOSAL AS A CARBONATE MINERAL: OPTIMIZING REACTION PROCESS DESIGN; A

International Nuclear Information System (INIS)

M.J. McKelvy; R. Sharma; A.V.G. Chizmeshya; H. Bearat; R.W. Carpenter

2001-01-01

Fossil fuels, especially coal, can support the energy demands of the world for centuries to come, if the environmental problems associated with CO(sub 2) emissions can be overcome. Permanent and safe methods for CO(sub 2) capture and disposal/storage need to be developed. Mineralization of stationary-source CO(sub 2) emissions as carbonates can provide such safe capture and long-term sequestration. Mg-rich lamellar-hydroxide based minerals (e.g., brucite and serpentine) offer a class of widely available, low-cost materials, with intriguing mineral carbonation potential. Carbonation of such materials inherently involves dehydroxylation, which can disrupt the material down to the atomic level. As such, controlled dehydroxylation, before and/or during carbonation, may provide an important parameter for enhancing carbonation reaction processes. Mg(OH)(sub 2) was chosen as the model material for investigating lamellar hydroxide mineral dehydroxylation/carbonation mechanisms due to (i) its structural and chemical simplicity, (ii) interest in Mg(OH)(sub 2) gas-solid carbonation as a potentially cost-effective CO(sub 2) mineral sequestration process component, and (iii) its structural and chemical similarity to other lamellar-hydroxide-based minerals (e.g., serpentine-based minerals) whose carbonation reaction processes are being explored due to their low-cost CO(sub 2) sequestration potential. Fundamental understanding of the mechanisms that govern dehydroxylation/carbonation processes is essential for minimizing the cost of any lamellar-hydroxide-based mineral carbonation sequestration process. This report covers the third year progress of this grant, as well as providing an integrated overview of the progress in years 1-3, as we have been granted a one-year no-cost extension to wrap up a few studies and publications to optimize project impact

Potential and economics of CO{sub 2} sequestration; Sequestration du CO{sub 2}: faisabilite et cout

Energy Technology Data Exchange (ETDEWEB)

Jean-Baptiste, Ph.; Ciais, Ph.; Orr, J. [CEA Saclay, 91 - Gif sur Yvette (France). Direction des Sciences de la Matiere; Ducroux, R. [Centre d' Initiative et de Recherche sur l' Energie et l' Environnement, CIRENE, 91 - Palaiseau (France)

2001-07-01

Increasing atmospheric level of greenhouse gases are causing global warming and putting at risk the global climate system. The main anthropogenic greenhouse gas is CO{sub 2}. Some techniques could be used to reduced CO{sub 2} emission and stabilize atmospheric CO{sub 2} concentration, including i) energy savings and energy efficiency, ii) switch to lower carbon content fuels (natural gas) and use energy sources with zero CO{sub 2} emissions such as renewable or nuclear energy, iii) capture and store CO{sub 2} from fossil fuels combustion, and enhance the natural sinks for CO{sub 2} (forests, soils, ocean...). The purpose of this report is to provide an overview of the technology and cost for capture and storage of CO{sub 2} and to review the various options for CO{sub 2} sequestration by enhancing natural carbon sinks. Some of the factors which will influence application, including environmental impact, cost and efficiency, are discussed. Capturing CO{sub 2} and storing it in underground geological reservoirs appears as the best environmentally acceptable option. It can be done with existing technology, however, substantial R and D is needed to improve available technology and to lower the cost. Applicable to large CO{sub 2} emitting industrial facilities such as power plants, cement factories, steel industry, etc., which amount to about 30% of the global anthropic CO{sub 2} emission, it represents a valuable tool in the baffle against global warming. About 50% of the anthropic CO{sub 2} is being naturally absorbed by the biosphere and the ocean. The 'natural assistance' provided by these two large carbon reservoirs to the mitigation of climate change is substantial. The existing natural sinks could be enhanced by deliberate action. Given the known and likely environmental consequences, which could be very damaging indeed, enhancing ocean sinks does not appears as a satisfactory option. In contrast, the promotion of land sinks through demonstrated carbon

Potential for CO2 sequestration and Enhanced Coalbed Methane production in the Netherlands

International Nuclear Information System (INIS)

Hamelinck, C.N.; Faaij, A.P.C.; Ruijg, G.J.; Jansen, D.; Pagnier, H.; Van Bergen, F.; Wolf, K.H.; Barzandji, O.; Bruining, H.; Schreurs, H.

2001-03-01

The technical and economic feasibility of ECBM (Enhanced Coal Bed Methane) in the Netherlands are explored. The potential and the economic performance are worked out for several ECBM recovery concepts and technological issues are outlined. The research includes the following main activities: Inventory of CO2 sources in the Netherlands and techno-economic analysis of CO2 removal and transport. Several scenarios for CO2 transport of different capacities and distances will be assessed. ECBM production locations are determined by analysis of coal reserves and their characteristics. Four potential areas are assessed: one in eastern Gelderland, two in Limburg and one in Zeeland. Description of ECBM theory and production technology resulting in a time dependent model for ECBM production and CO2 injection. Selection and description of various ECBM production/CO2 sequestration systems. Systems considered include direct delivery of methane to the natural gas grid, production of power (on various scales) and hydrogen. Information from the location assessment is combined with modelling results. Costs of CO2 sequestration are calculated for various scales and configurations. Evaluation of main uncertainties, environmental impacts and sensitivity analyses. Comparison of CBM production systems with reference systems and exploration of potential implementation schemes in the Dutch context. 72 refs

Activation of magnesium rich minerals as carbonation feedstock materials for CO2 sequestration

International Nuclear Information System (INIS)

Maroto-Valer, M.M.; Kuchta, M.E.; Zhang, Y.; Andresen, J.M.; Fauth, D.J.

2005-01-01

Mineral carbonation, the reaction of magnesium-rich minerals such as olivine and serpentine with CO 2 to form stable mineral carbonates, is a novel and promising approach to carbon sequestration. However, the preparation of the minerals prior to carbonation can be energy intensive, where some current studies have been exploring extensive pulverization of the minerals below 37 μm, heat treatment of minerals up to 650 o C, prior separation of CO 2 from flue gases, and carbonation at high pressures, temperatures and long reaction times of up to 125 atm, 185 o C and 6 h, respectively. Thus, the objective of the mineral activation concept is to promote and accelerate carbonation reaction rates and efficiencies through surface activation to the extent that such rigorous reaction conditions were not required. The physical activations were performed with air and steam, while chemical activations were performed with a suite of acids and bases. The parent serpentine, activated serpentines, and carbonation products were characterized to determine their surface properties and assess their potential as carbonation minerals. The results indicate that the surface area of the raw serpentine, which is approximately 8 m 2 /g, can be increased through physical and chemical activation methods to over 330 m 2 /g. The chemical activations were more effective than the physical activations at increasing the surface area, with the 650 o C steam activated serpentine presenting a surface area of only 17 m 2 /g. Sulfuric acid was the most effective acid used during the chemical activations, resulting in surface areas greater than 330 m 2 /g. Several of the samples produced underwent varying degrees of carbonation. The steam activated serpentine underwent a 60% conversion to magnesite at 155 o C and 126 atm in 1 h, while the parent sample only exhibited a 7% conversion. The most promising results came from the carbonation of the extracted Mg(OH) 2 solution, where, based on the amount of

Evaluation of the CO2 sequestration capacity for coal fly ash using a flow-through column reactor under ambient conditions

International Nuclear Information System (INIS)

Jo, Ho Young; Ahn, Joon-Hoon; Jo, Hwanju

2012-01-01

Highlights: ► A conceptual in-situ mineral carbonation method using a coal ash pond is proposed. ► CO 2 uptake occurred by carbonation reaction of CO 2 with Ca 2+ ions from coal fly ash. ► The CO 2 sequestration capacity was affected by the solid dosage. ► Seawater can be used as a solvent for mineral carbonation of coal fly ash. - Abstract: An in-situ CO 2 sequestration method using coal ash ponds located in coastal regions is proposed. The CO 2 sequestration capacity of coal fly ash (CFA) by mineral carbonation was evaluated in a flow-through column reactor under various conditions (solid dosage: 100–330 g/L, CO 2 flow rate: 20–80 mL/min, solvent type: deionized (DI) water, 1 M NH 4 Cl solution, and seawater). The CO 2 sequestration tests were conducted on CFA slurries using flow-through column reactors to simulate more realistic flow-through conditions. The CO 2 sequestration capacity increased when the solid dosage was increased, whereas it was affected insignificantly by the CO 2 flow rate. A 1 M NH 4 Cl solution was the most effective solvent, but it was not significantly different from DI water or seawater. The CO 2 sequestration capacity of CFA under the flow-through conditions was approximately 0.019 g CO 2 /g CFA under the test conditions (solid dosage: 333 g/L, CO 2 flow rate: 40 mL/min, and solvent: seawater).

Geologic CO2 Sequestration: Predicting and Confirming Performance in Oil Reservoirs and Saline Aquifers

Science.gov (United States)

Johnson, J. W.; Nitao, J. J.; Newmark, R. L.; Kirkendall, B. A.; Nimz, G. J.; Knauss, K. G.; Ziagos, J. P.

2002-05-01

Reducing anthropogenic CO2 emissions ranks high among the grand scientific challenges of this century. In the near-term, significant reductions can only be achieved through innovative sequestration strategies that prevent atmospheric release of large-scale CO2 waste streams. Among such strategies, injection into confined geologic formations represents arguably the most promising alternative; and among potential geologic storage sites, oil reservoirs and saline aquifers represent the most attractive targets. Oil reservoirs offer a unique "win-win" approach because CO2 flooding is an effective technique of enhanced oil recovery (EOR), while saline aquifers offer immense storage capacity and widespread distribution. Although CO2-flood EOR has been widely used in the Permian Basin and elsewhere since the 1980s, the oil industry has just recently become concerned with the significant fraction of injected CO2 that eludes recycling and is therefore sequestered. This "lost" CO2 now has potential economic value in the growing emissions credit market; hence, the industry's emerging interest in recasting CO2 floods as co-optimized EOR/sequestration projects. The world's first saline aquifer storage project was also catalyzed in part by economics: Norway's newly imposed atmospheric emissions tax, which spurred development of Statoil's unique North Sea Sleipner facility in 1996. Successful implementation of geologic sequestration projects hinges on development of advanced predictive models and a diverse set of remote sensing, in situ sampling, and experimental techniques. The models are needed to design and forecast long-term sequestration performance; the monitoring techniques are required to confirm and refine model predictions and to ensure compliance with environmental regulations. We have developed a unique reactive transport modeling capability for predicting sequestration performance in saline aquifers, and used it to simulate CO2 injection at Sleipner; we are now

Potential and economics of CO2 sequestration

International Nuclear Information System (INIS)

Jean-Baptiste, Ph.; Ciais, Ph.; Orr, J.

2001-01-01

Increasing atmospheric level of greenhouse gases are causing global warming and putting at risk the global climate system. The main anthropogenic greenhouse gas is CO 2 . Some techniques could be used to reduced CO 2 emission and stabilize atmospheric CO 2 concentration, including i) energy savings and energy efficiency, ii) switch to lower carbon content fuels (natural gas) and use energy sources with zero CO 2 emissions such as renewable or nuclear energy, iii) capture and store CO 2 from fossil fuels combustion, and enhance the natural sinks for CO 2 (forests, soils, ocean...). The purpose of this report is to provide an overview of the technology and cost for capture and storage of CO 2 and to review the various options for CO 2 sequestration by enhancing natural carbon sinks. Some of the factors which will influence application, including environmental impact, cost and efficiency, are discussed. Capturing CO 2 and storing it in underground geological reservoirs appears as the best environmentally acceptable option. It can be done with existing technology, however, substantial R and D is needed to improve available technology and to lower the cost. Applicable to large CO 2 emitting industrial facilities such as power plants, cement factories, steel industry, etc., which amount to about 30% of the global anthropic CO 2 emission, it represents a valuable tool in the baffle against global warming. About 50% of the anthropic CO 2 is being naturally absorbed by the biosphere and the ocean. The 'natural assistance' provided by these two large carbon reservoirs to the mitigation of climate change is substantial. The existing natural sinks could be enhanced by deliberate action. Given the known and likely environmental consequences, which could be very damaging indeed, enhancing ocean sinks does not appears as a satisfactory option. In contrast, the promotion of land sinks through demonstrated carbon-storing approach to agriculture, forests and land management could

Investigating Natural Analogues for Co{sub 2} Sequestration in Ultra Mafic Rocks: A Reactive Transport Modelling Approach

Energy Technology Data Exchange (ETDEWEB)

Gherardi, F. [Istituto di Geoscienze e Georisorse, Consiglio Nazionale delle Ricerche, Pisa (Italy)

2013-07-15

Serpentinites of Ligurian ophiolites are studied as natural analogues for CO{sub 2} mineral sequestration in Italy. Mineralogical and geochemical observations indicate that silicification and carbonation are typical alteration processes induced by the interaction of CO{sub 2} charged fluids with pristine ultramafic rocks. Multicomponent reactive transport models have been applied to reproduce natural patterns and investigate carbon sequestration efficiency under high P{sub CO2} conditions. Temporal changes in porosity and permeability are predicted to affect the spatial and temporal occurrence of secondary minerals. The feedback between mineralogical transformations and transport properties of the geological media emerges as a key factor controlling the mineral carbonation potential of the investigated ultramafic rocks. (author)

Procedure to use phosphogypsum industrial waste for mineral CO{sub 2} sequestration

Energy Technology Data Exchange (ETDEWEB)

Cardenas-Escudero, C. [Departamento de Fisica de la Materia Condensada, Facultad de Fisica, Universidad de Sevilla, Av. Reina Mercedes s/n, 41012 Seville (Spain); Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain); Morales-Florez, V., E-mail: victor.morales@icmse.csic.es [Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain); Perez-Lopez, R. [Departamento de Geologia, Facultad de Ciencias Experimentales, Universidad de Huelva, Campus Universitario Campus del Carmen, Avenida de las Fuerzas Armadas, 21071 Huelva (Spain); Instituto de Diagnostico Ambiental y Estudios del Agua (IDAeA-CSIC), Jordi Girona 18, 08034 Barcelona (Spain); Santos, A. [Departamento de Ciencias de la Tierra, Universidad de Cadiz, Campus del Rio San Pedro, Av. Republica Saharaui s/n, 11510 Puerto Real (Spain); Esquivias, L. [Departamento de Fisica de la Materia Condensada, Facultad de Fisica, Universidad de Sevilla, Av. Reina Mercedes s/n, 41012 Seville (Spain); Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain)

2011-11-30

Highlights: Black-Right-Pointing-Pointer Phosphogypsum wastes are proposed to reduce CO{sub 2} greenhouse gas emissions. Black-Right-Pointing-Pointer Phosphogypsum dissolution with NaOH results in Ca(OH){sub 2} precipitation and Na{sub 2}SO{sub 4}. Black-Right-Pointing-Pointer Aqueous carbonation of Ca(OH){sub 2} with CO{sub 2} results in the CaCO{sub 3} precipitation. Black-Right-Pointing-Pointer Metals contained in the phosphogypsum are transferred to the final calcite. Black-Right-Pointing-Pointer Applications of CaCO{sub 3} and Na{sub 2}SiO{sub 4} by-products are proposed to improve viability. - Abstract: Industrial wet phosphoric acid production in Huelva (SW Spain) has led to the controversial stockpiling of waste phosphogypsum by-products, resulting in the release of significant quantities of toxic impurities in salt marshes in the Tinto river estuary. In the framework of the fight against global climate change and the effort to reduce carbon dioxide emissions, a simple and efficient procedure for CO{sub 2} mineral sequestration is presented in this work, using phosphogypsum waste as a calcium source. Our results demonstrate the high efficiency of portlandite precipitation by phosphogypsum dissolution using an alkaline soda solution. Carbonation experiments performed at ambient pressure and temperature resulted in total conversion of the portlandite into carbonate. The fate of trace elements present in the phosphogypsum waste was also investigated, and trace impurities were found to be completely transferred to the final calcite. We believe that the procedure proposed here should be considered not only as a solution for reducing old stockpiles of phosphogypsum wastes, but also for future phosphoric acid and other gypsum-producing industrial processes, resulting in more sustainable production.

Numerical simulation of CO2 disposal by mineral trapping in deep aquifers

International Nuclear Information System (INIS)

Xu Tianfu; Apps, John A.; Pruess, Karsten

2004-01-01

Carbon dioxide disposal into deep aquifers is a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO 2 disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO 2 injection, the authors have analyzed the impact of CO 2 immobilization through carbonate mineral precipitation. Batch reaction modeling of the geochemical evolution of 3 different aquifer mineral compositions in the presence of CO 2 at high pressure were performed. The modeling considered the following important factors affecting CO 2 sequestration: (1) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, (2) CO 2 solubility dependence on pressure, temperature and salinity of the system, and (3) redox processes that could be important in deep subsurface environments. The geochemical evolution under CO 2 injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO 2 sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO 2 that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO 2 dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of Fe(III) mineral precursors such as goethite or glauconite. The accumulation of carbonates in the rock matrix leads to a considerable decrease in porosity. This in turn adversely affects permeability and fluid flow in the aquifer. The numerical experiments described here provide useful insight into sequestration mechanisms, and their controlling geochemical conditions and parameters

Aluminosilicate Dissolution and Silicate Carbonation during Geologic CO2 Sequestration

Science.gov (United States)

Min, Yujia

Geologic CO2 sequestration (GCS) is considered a promising method to reduce anthropogenic CO2 emission. Assessing the supercritical CO2 (scCO2) gas or liquid phase water (g, l)-mineral interactions is critical to evaluating the viability of GCS processes. This work contributes to our understanding of geochemical reactions at CO 2-water (g, l)-mineral interfaces, by investigating the dissolution of aluminosilicates in CO2-acidified water (l). Plagioclase and biotite were chosen as model minerals in reservoir rock and caprock, respectively. To elucidate the effects of brine chemistry, first, the influences of cations in brine including Na, Ca, and K, have been investigated. In addition to the cations, the effects of abundant anions including sulfate and oxalate were also examined. Besides the reactions in aqueous phase, we also examine the carbonation of silicates in water (g)-bearing supercritical CO2 (scCO2) under conditions relevant to GCS. For the metal carbonation, in particular, the effects of particle sizes, water, temperature, and pressure on the carbonation of wollastonite were systematically examined. For understanding the cations effects in brine, the impacts of Na concentrations up to 4 M on the dissolution of plagioclase and biotite were examined. High concentrations of Na significantly inhibited plagioclase dissolution by competing adsorption with proton and suppressing proton-promoted dissolution. Ca has a similar effect to Na, and their effects did not suppress each other when Na and Ca co-existed. For biotite, the inhibition effects of Na coupled with an enhancing effect due to ion exchange reaction between Na and interlayer K, which cracked the basal surfaces of biotite. The K in aqueous phase significantly inhibited the dissolution. If the biotite is equilibrated with NaCl solutions initially, the biotite dissolved faster than the original biotite and the dissolution was inhibited by Na and K in brine. The outcomes improve our current knowledge of

Integrating Steel Production with Mineral Carbon Sequestration

Energy Technology Data Exchange (ETDEWEB)

Klaus Lackner; Paul Doby; Tuncel Yegulalp; Samuel Krevor; Christopher Graves

2008-05-01

The objectives of the project were (i) to develop a combination iron oxide production and carbon sequestration plant that will use serpentine ores as the source of iron and the extraction tailings as the storage element for CO2 disposal, (ii) the identification of locations within the US where this process may be implemented and (iii) to create a standardized process to characterize the serpentine deposits in terms of carbon disposal capacity and iron and steel production capacity. The first objective was not accomplished. The research failed to identify a technique to accelerate direct aqueous mineral carbonation, the limiting step in the integration of steel production and carbon sequestration. Objective (ii) was accomplished. It was found that the sequestration potential of the ultramafic resource surfaces in the US and Puerto Rico is approximately 4,647 Gt of CO2 or over 500 years of current US production of CO2. Lastly, a computer model was developed to investigate the impact of various system parameters (recoveries and efficiencies and capacities of different system components) and serpentinite quality as well as incorporation of CO2 from sources outside the steel industry.

Evaluation of the CO{sub 2} sequestration capacity for coal fly ash using a flow-through column reactor under ambient conditions

Energy Technology Data Exchange (ETDEWEB)

Jo, Ho Young, E-mail: hyjo@korea.ac.kr [Department of Earth and Environmental Sciences, Korea University, Anam-dong, Seongbuk-gu, Seoul 136-713 (Korea, Republic of); Ahn, Joon-Hoon; Jo, Hwanju [Department of Earth and Environmental Sciences, Korea University, Anam-dong, Seongbuk-gu, Seoul 136-713 (Korea, Republic of)

2012-11-30

Highlights: Black-Right-Pointing-Pointer A conceptual in-situ mineral carbonation method using a coal ash pond is proposed. Black-Right-Pointing-Pointer CO{sub 2} uptake occurred by carbonation reaction of CO{sub 2} with Ca{sup 2+} ions from coal fly ash. Black-Right-Pointing-Pointer The CO{sub 2} sequestration capacity was affected by the solid dosage. Black-Right-Pointing-Pointer Seawater can be used as a solvent for mineral carbonation of coal fly ash. - Abstract: An in-situ CO{sub 2} sequestration method using coal ash ponds located in coastal regions is proposed. The CO{sub 2} sequestration capacity of coal fly ash (CFA) by mineral carbonation was evaluated in a flow-through column reactor under various conditions (solid dosage: 100-330 g/L, CO{sub 2} flow rate: 20-80 mL/min, solvent type: deionized (DI) water, 1 M NH{sub 4}Cl solution, and seawater). The CO{sub 2} sequestration tests were conducted on CFA slurries using flow-through column reactors to simulate more realistic flow-through conditions. The CO{sub 2} sequestration capacity increased when the solid dosage was increased, whereas it was affected insignificantly by the CO{sub 2} flow rate. A 1 M NH{sub 4}Cl solution was the most effective solvent, but it was not significantly different from DI water or seawater. The CO{sub 2} sequestration capacity of CFA under the flow-through conditions was approximately 0.019 g CO{sub 2}/g CFA under the test conditions (solid dosage: 333 g/L, CO{sub 2} flow rate: 40 mL/min, and solvent: seawater).

FY 1999 survey report on the survey of the trend of the development of CO2 underground sequestration; 1999 nendo CO{sub 2} chichu kakuri gijutsu ni kansuru kaihatsu doko chosa hokokusho

Energy Technology Data Exchange (ETDEWEB)

NONE

2000-03-01

Paying attention to the CO2 sequestration technology, especially underground sequestration technology, this survey proposed a model case of the CO2 underground project including CO2 emission sources, means of transportation and CO2 injection equipment in terms of economical efficiency, environmental loads and technology in Japan and in other areas, and also studied projects on underground sequestration which are viable under CTI and other frameworks. The sequestration technology is classified into ocean sequestration, biological sequestration, underground sequestration and material sequestration. The underground sequestration is classified into the enhanced oil recovery, enhanced coal bed methane recovery, depleted oil/gas reservoir sequestration, and deep aquifer sequestration. The cost of sequestration is $100-300 per 1 ton of CO2, and is low in competitiveness at present. However, in the tertiary oil recovery and coal bed methane recovery, it costs nothing for CO2 reduction. As to the enhanced oil recovery, 66 projects were carried out in 1998 in the U.S. As to the enhanced coal bed methane recovery, projects in Canada, the U.S., and the U.K. As to the deep aquifer sequestration, one project in Norway. Concerning NEDO's project, there are great possibilities in aquifer and depleted oil/gas reservoir sequestration. (NEDO)

Numerical Study on CO2-Brine-Rock Interaction of Enhanced Geothermal Systems with CO2 as Heat Transmission Fluid

Directory of Open Access Journals (Sweden)

Wan Yuyu

2016-01-01

Full Text Available Enhanced Geothermal Systems (EGS with CO2 instead of water as heat transmission fluid is an attractive concept for both geothermal resources development and CO2 geological sequestration. Previous studies show that CO2 has lots of favorable properties as heat transmission fluid and also can offer geologic storage of CO2 as an ancillary benefit. However, after CO2 injection into geological formations, chemical reaction between brine and rock can change chemical characteristics of saline and properties of rock such as porosity and permeability. Is this advantage or disadvantage for EGS operating? To answer this question, we have performed chemically reactive transport modeling to investigate fluid-rock interactions and CO2 mineral carbonation of Enhanced Geothermal Systems (EGS site at Desert Peak (Nevada operated with CO2. The simulation results show that (1 injection CO2 can create a core zone fulfilled with CO2 as main working domain for EGS, and (2 CO2 storage can induced self-enhancing alteration of EGS.

Analysis of mineral trapping for CO{sub 2} disposal in deep aquifers

Energy Technology Data Exchange (ETDEWEB)

Xu, Tianfu; Apps, John A.; Pruess, Karsten

2001-07-20

CO{sub 2} disposal into deep aquifers has been suggested as a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO{sub 2} disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO{sub 2} injection, we have analyzed the impact of CO{sub 2} immobilization through carbonate precipitation. A survey of all major classes of rock-forming minerals, whose alteration would lead to carbonate precipitation, indicated that very few minerals are present in sufficient quantities in aquifer host rocks to permit significant sequestration of CO{sub 2}. We performed batch reaction modeling of the geochemical evolution of three different aquifer mineralogies in the presence of CO{sub 2} at high pressure. Our modeling considered (1) redox processes that could be important in deep subsurface environments, (2) the presence of organic matter, (3) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, and (4) CO{sub 2} solubility dependence on pressure, temperature and salinity of the system. The geochemical evolution under both natural background and CO{sub 2} injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO{sub 2} sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO{sub 2} that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO{sub 2} dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of ferric mineral precursors such as glauconite, which in turn is dependent on the reactivity of associated organic material. The accumulation of carbonates in

Southwestern Regional Partnership For Carbon Sequestration (Phase 2): Pump Canyon CO2-ECBM/Sequestration Demonstration, San Juan Basin, New Mexico

International Nuclear Information System (INIS)

2010-01-01

Within the Southwest Regional Partnership on Carbon Sequestration (SWP), three demonstrations of geologic CO 2 sequestration are being performed -- one in an oilfield (the SACROC Unit in the Permian basin of west Texas), one in a deep, unmineable coalbed (the Pump Canyon site in the San Juan basin of northern New Mexico), and one in a deep, saline reservoir (underlying the Aneth oilfield in the Paradox basin of southeast Utah). The Pump Canyon CO 2 -enhanced coalbed methane (CO 2 /ECBM) sequestration demonstration project plans to demonstrate the effectiveness of CO 2 sequestration in deep, unmineable coal seams via a small-scale geologic sequestration project. The site is located in San Juan County, northern New Mexico, just within the limits of the high-permeability fairway of prolific coalbed methane production. The study area for the SWP project consists of 31 coalbed methane production wells located in a nine section area. CO 2 was injected continuously for a year and different monitoring, verification and accounting (MVA) techniques were implemented to track the CO 2 movement inside and outside the reservoir. Some of the MVA methods include continuous measurement of injection volumes, pressures and temperatures within the injection well, coalbed methane production rates, pressures and gas compositions collected at the offset production wells, and tracers in the injected CO 2 . In addition, time-lapse vertical seismic profiling (VSP), surface tiltmeter arrays, a series of shallow monitoring wells with a regular fluid sampling program, surface measurements of soil composition, CO 2 fluxes, and tracers were used to help in tracking the injected CO 2 . Finally, a detailed reservoir model was constructed to help reproduce and understand the behavior of the reservoir under production and injection operation. This report summarizes the different phases of the project, from permitting through site closure, and gives the results of the different MVA techniques.

Experimental investigation of CO2-brine-rock interactions at elevated temperature and pressure: Implications for CO2 sequestration in deep-saline aquifers

Science.gov (United States)

Rosenbauer, R.J.; Koksalan, T.; Palandri, J.L.

2005-01-01

Deep-saline aquifers are potential repositories for excess CO2, currently being emitted to the atmosphere from anthropogenic activities, but the reactivity of supercritical CO2 with host aquifer fluids and formation minerals needs to be understood. Experiments reacting supercritical CO2 with natural and synthetic brines in the presence and absence of limestone and plagioclase-rich arkosic sandstone showed that the reaction of CO2-saturated brine with limestone results in compositional, mineralogical, and porosity changes in the aquifer fluid and rock that are dependent on initial brine composition, especially dissolved calcium and sulfate. Experiments reacting CO2-saturated, low-sulfate brine with limestone dissolved 10% of the original calcite and increased rock porosity by 2.6%. Experiments reacting high-sulfate brine with limestone, both in the presence and absence of supercritical CO2, were characterized by the precipitation of anhydrite, dolomitization of the limestone, and a final decrease in porosity of 4.5%. However, based on favorable initial porosity changes of about 15% due to the dissolution of calcite, the combination of CO2 co-injection with other mitigation strategies might help alleviate some of the well-bore scale and formation-plugging problems near the injection zone of a brine disposal well in Paradox Valley, Colorado, as well as provide a repository for CO2. Experiments showed that the solubility of CO2 is enhanced in brine in the presence of limestone by 9% at 25 ??C and 6% at 120 ??C and 200 bar relative to the brine itself. The solubility of CO2 is enhanced also in brine in the presence of arkosic sandstone by 5% at 120 ??C and 300 bar. The storage of CO 2 in limestone aquifers is limited to only ionic and hydraulic trapping. However, brine reacted with supercritical CO2 and arkose yielded fixation and sequestration of CO2 in carbonate mineral phases. Brine desiccation was observed in all experiments containing a discrete CO2 phase

Continuing Studies on Direct Aqueous Mineral Carbonation of CO{sub 2} Sequestration

Energy Technology Data Exchange (ETDEWEB)

O' Connor, W.K.; Dahlin, D.C.; Nilsen, D.N.; Gerdemann, S.J.; Rush, G.E.; Penner, L.R.; Walters, R.P.; Turner, P.C.

2002-03-04

Direct aqueous mineral carbonation has been investigated as a process to convert gaseous CO{sub 2} into a geologically stable, solid final form. The process utilizes a solution of sodium bicarbonate (NaHCO{sub 3}), sodium chloride (NaCl), and water, mixed with a mineral reactant, such as olivine (Mg{sub 2}SiO{sub 4}) or serpentine [Mg{sub 3}Si{sub 2}O{sub 5}(OH){sub 4}]. Carbon dioxide is dissolved into this slurry, by diffusion through the surface and gas dispersion within the aqueous phase. The process includes dissolution of the mineral and precipitation of the magnesium carbonate mineral magnesite (MgCO{sub 3}) in a single unit operation. Activation of the silicate minerals has been achieved by thermal and mechanical means, resulting in up to 80% stoichiometric conversion of the silicate to the carbonate within 30 minutes. Heat treatment of the serpentine, or attrition grinding of the olivine and/or serpentine, appear to activate the minerals by the generation of a non-crystalline phase. Successful conversion to the carbonate has been demonstrated at ambient temperature and relatively low (10 atm) partial pressure of CO{sub 2} (P{sub CO2}). However, optimum results have been achieved using the bicarbonate-bearing solution, and high P{sub CO2}. Specific conditions include: 185 C; P{sub CO2}=150 atm; 30% solids. Studies suggest that the mineral dissolution rate is not solely surface controlled, while the carbonate precipitation rate is primarily dependent on the bicarbonate concentration of the slurry. Current and future activities include further examination of the reaction pathways and pretreatment options, the development of a continuous flow reactor, and an evaluation of the economic feasibility of the process.

Analysis of CO2 Separation from Flue Gas, Pipeline Transportation, and Sequestration in Coal

Energy Technology Data Exchange (ETDEWEB)

Eric P. Robertson

2007-09-01

This report was written to satisfy a milestone of the Enhanced Coal Bed Methane Recovery and CO2 Sequestration task of the Big Sky Carbon Sequestration project. The report begins to assess the costs associated with separating the CO2 from flue gas and then injecting it into an unminable coal seam. The technical challenges and costs associated with CO2 separation from flue gas and transportation of the separated CO2 from the point source to an appropriate sequestration target was analyzed. The report includes the selection of a specific coal-fired power plant for the application of CO2 separation technology. An appropriate CO2 separation technology was identified from existing commercial technologies. The report also includes a process design for the chosen technology tailored to the selected power plant that used to obtain accurate costs of separating the CO2 from the flue gas. In addition, an analysis of the costs for compression and transportation of the CO2 from the point-source to an appropriate coal bed sequestration site was included in the report.

Analysis of mineral trapping for CO(sub 2) disposal in deep aquifers; TOPICAL

International Nuclear Information System (INIS)

Xu, Tianfu; Apps, John A.; Pruess, Karsten

2001-01-01

CO(sub 2) disposal into deep aquifers has been suggested as a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO(sub 2) disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO(sub 2) injection, we have analyzed the impact of CO(sub 2) immobilization through carbonate precipitation. A survey of all major classes of rock-forming minerals, whose alteration would lead to carbonate precipitation, indicated that very few minerals are present in sufficient quantities in aquifer host rocks to permit significant sequestration of CO(sub 2). We performed batch reaction modeling of the geochemical evolution of three different aquifer mineralogies in the presence of CO(sub 2) at high pressure. Our modeling considered (1) redox processes that could be important in deep subsurface environments, (2) the presence of organic matter, (3) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, and (4) CO(sub 2) solubility dependence on pressure, temperature and salinity of the system. The geochemical evolution under both natural background and CO(sub 2) injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO(sub 2) sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO(sub 2) that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO(sub 2) dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of ferric mineral precursors such as glauconite, which in turn is dependent on the reactivity of associated organic material. The accumulation of carbonates in

Exploration of public acceptance regarding CO2 underground sequestration technologies

International Nuclear Information System (INIS)

Uno, M.; Tokushige, K.; Mori, Y.; Furukawa, A.

2005-01-01

Mechanisms for gaining public acceptance of carbon dioxide (CO 2 ) aquifer sequestration were investigated through the use of questionnaires and focus group interviews. The study was performed as part of a CO 2 sequestration technology promotion project in Japan. The questionnaire portion of the study was conducted to determine public opinions and the extent of public awareness of CO 2 sequestration technologies. Questionnaires were distributed to undergraduate students majoring in environmental sociology. Participants were provided with newspaper articles related to CO 2 sequestration. The focus group study was conducted to obtain qualitative results to complement findings from the questionnaire survey. Results of the survey suggested that many participants were not particularly concerned about global warming, and had almost no knowledge about CO 2 sequestration. The opinions of some students were influenced by an awareness of similar types of facilities located near their homes. Attitudes were also influenced by the newspaper articles provided during the focus group sessions. However, many older participants did not trust information presented to them in newspaper format. Results suggested that many people identified afforestation as an alternative technology to CO 2 sequestration, and tended to think of CO 2 in negative terms as it contributed to global warming. Some participants assumed that CO 2 was harmful. The majority of respondents agreed with the development of CO 2 sequestration technologies as part of a program of alternative emissions abatement technologies. The provision of detailed information concerning CO 2 sequestration did not completely remove anxieties concerning the technology's potential negative impacts. It was concluded that a confident communications strategy is needed to persuade Japanese residents of the need to implement CO 2 sequestration technologies. 11 refs., 2 figs

A method for permanent CO2 mineral carbonation

Energy Technology Data Exchange (ETDEWEB)

Dahlin, David C.; O' Connor, William K.; Nilsen, David N.; Rush, G.E.; Walters, Richard P.; Turner, Paul C.

2000-01-01

The Albany Research Center (ARC) of the U.S. Department of Energy (DOE) has been conducting research to investigate the feasibility of mineral carbonation as a method for carbon dioxide (CO2) sequestration. The research is part of a Mineral Carbonation Study Program within the Office of Fossil Energy in DOE. Other participants in this Program include DOE?s Los Alamos National Laboratory and National Energy Technology Laboratory, Arizona State University, and Science Applications International Corporation. The research has focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC reacts a slurry of magnesium silicate mineral with supercritical CO2 to produce a solid magnesium carbonate product. To date, olivine and serpentine have been used as the mineral reactant, but other magnesium silicates could be used as well. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and consequently, these results may also be applicable to strategies for in-situ geological sequestration. Baseline tests were begun in distilled water on ground products of foundry-grade olivine. Tests conducted at 150 C and subcritical CO2 pressures (50 atm) resulted in very slow conversion to carbonate. Increasing the partial pressure of CO2 to supercritical (>73 atm) conditions, coupled with agitation of the slurry and gas dispersion within the water column, resulted in significant improvement in the extent of reaction in much shorter reaction times. A change from distilled water to a bicarbonate/salt solution further improved the rate and extent of reaction. When serpentine, a hydrated mineral, was used instead of olivine, extent of reaction was poor until heat treatment was included prior to the carbonation reaction. Removal of the chemically bound water resulted in conversion to carbonate similar to those obtained with olivine. Recent results have shown that conversions of nearly 80 pct are achievable after 30 minutes

Potential for iron oxides to control metal releases in CO2 sequestration scenarios

Science.gov (United States)

Berger, P.M.; Roy, W.R.

2011-01-01

The potential for the release of metals into groundwater following the injection of carbon dioxide (CO2) into the subsurface during carbon sequestration projects remains an open research question. Changing the chemical composition of even the relatively deep formation brines during CO2 injection and storage may be of concern because of the recognized risks associated with the limited potential for leakage of CO2-impacted brine to the surface. Geochemical modeling allows for proactive evaluation of site geochemistry before CO2 injection takes place to predict whether the release of metals from iron oxides may occur in the reservoir. Geochemical modeling can also help evaluate potential changes in shallow aquifers were CO2 leakage to occur near the surface. In this study, we created three batch-reaction models that simulate chemical changes in groundwater resulting from the introduction of CO2 at two carbon sequestration sites operated by the Midwest Geological Sequestration Consortium (MGSC). In each of these models, we input the chemical composition of groundwater samples into React??, and equilibrated them with selected mineral phases and CO 2 at reservoir pressure and temperature. The model then simulated the kinetic reactions with other mineral phases over a period of up to 100 years. For two of the simulations, the water was also at equilibrium with iron oxide surface complexes. The first model simulated a recently completed enhanced oil recovery (EOR) project in south-central Illinois in which the MGSC injected into, and then produced CO2, from a sandstone oil reservoir. The MGSC afterwards periodically measured the brine chemistry from several wells in the reservoir for approximately two years. The sandstone contains a relatively small amount of iron oxide, and the batch simulation for the injection process showed detectable changes in several aqueous species that were attributable to changes in surface complexation sites. After using the batch reaction

Reduction of the greenhouse effect by geological mineral in-situ sequestration of CO2 in basic rocks: bibliographic synthesis and possibilities in France. Final report

International Nuclear Information System (INIS)

Marechal, J.C.; Lachassagne, P.

2004-01-01

The report constitutes a first bibliographic study defining the environments the most adapted to the geological mineral in-situ sequestration of CO 2 . For each environment the lithology and the rocks permeability and porosity are analyzed. Thus the possible rocks and deposits in France are presented. (A.L.B.)

Southwestern Regional Partnership For Carbon Sequestration (Phase 2) Pump Canyon CO2- ECBM/Sequestration Demonstration, San Juan Basin, New Mexico

Energy Technology Data Exchange (ETDEWEB)

Advanced Resources International

2010-01-31

Within the Southwest Regional Partnership on Carbon Sequestration (SWP), three demonstrations of geologic CO{sub 2} sequestration are being performed -- one in an oilfield (the SACROC Unit in the Permian basin of west Texas), one in a deep, unmineable coalbed (the Pump Canyon site in the San Juan basin of northern New Mexico), and one in a deep, saline reservoir (underlying the Aneth oilfield in the Paradox basin of southeast Utah). The Pump Canyon CO{sub 2}-enhanced coalbed methane (CO{sub 2}/ECBM) sequestration demonstration project plans to demonstrate the effectiveness of CO{sub 2} sequestration in deep, unmineable coal seams via a small-scale geologic sequestration project. The site is located in San Juan County, northern New Mexico, just within the limits of the high-permeability fairway of prolific coalbed methane production. The study area for the SWP project consists of 31 coalbed methane production wells located in a nine section area. CO{sub 2} was injected continuously for a year and different monitoring, verification and accounting (MVA) techniques were implemented to track the CO{sub 2} movement inside and outside the reservoir. Some of the MVA methods include continuous measurement of injection volumes, pressures and temperatures within the injection well, coalbed methane production rates, pressures and gas compositions collected at the offset production wells, and tracers in the injected CO{sub 2}. In addition, time-lapse vertical seismic profiling (VSP), surface tiltmeter arrays, a series of shallow monitoring wells with a regular fluid sampling program, surface measurements of soil composition, CO{sub 2} fluxes, and tracers were used to help in tracking the injected CO{sub 2}. Finally, a detailed reservoir model was constructed to help reproduce and understand the behavior of the reservoir under production and injection operation. This report summarizes the different phases of the project, from permitting through site closure, and gives the

Olivine Dissolution in Seawater: Implications for CO2 Sequestration through Enhanced Weathering in Coastal Environments

Science.gov (United States)

2017-01-01

Enhanced weathering of (ultra)basic silicate rocks such as olivine-rich dunite has been proposed as a large-scale climate engineering approach. When implemented in coastal environments, olivine weathering is expected to increase seawater alkalinity, thus resulting in additional CO2 uptake from the atmosphere. However, the mechanisms of marine olivine weathering and its effect on seawater–carbonate chemistry remain poorly understood. Here, we present results from batch reaction experiments, in which forsteritic olivine was subjected to rotational agitation in different seawater media for periods of days to months. Olivine dissolution caused a significant increase in alkalinity of the seawater with a consequent DIC increase due to CO2 invasion, thus confirming viability of the basic concept of enhanced silicate weathering. However, our experiments also identified several important challenges with respect to the detailed quantification of the CO2 sequestration efficiency under field conditions, which include nonstoichiometric dissolution, potential pore water saturation in the seabed, and the potential occurrence of secondary reactions. Before enhanced weathering of olivine in coastal environments can be considered an option for realizing negative CO2 emissions for climate mitigation purposes, these aspects need further experimental assessment. PMID:28281750

Carbon Dioxide (CO2 Sequestration In Bio-Concrete, An Overview

Directory of Open Access Journals (Sweden)

Faisal Alshalif A.

2017-01-01

Full Text Available The emission of CO2 into atmosphere which has increased rapidly in the last years has led to global warming. Therefore, in order to overcome the negative impacts on human and environment, the researchers focused mainly on the reduction and stabilization of CO2 which represent the main contributor in the increasing global warming. The natural capturing and conversion of CO2 from atmosphere is taken place by biological, chemical and physical processes. However, these processes need long time to cause a significant reduction in CO2. Recently, scientists shifted to use green technologies that aimed to produce concrete with high potential to adsorb CO2 in order to accelerate the reduction of CO2. In the present review the potential of bio-concrete to sequestrate CO2 based on carbonation process and as a function of carbonic anhydrase (CA is highlighted. The factors affecting CO2 sequestration in concrete and bacterial species are discussed. It is evident from the literatures, that the new trends to use bio-concrete might contribute in the reduction of CO2 and enhance the strength of non-reinforced concrete.

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

Nanoscale Chemical Processes Affecting Storage Capacities and Seals during Geologic CO2 Sequestration.

Science.gov (United States)

Jun, Young-Shin; Zhang, Lijie; Min, Yujia; Li, Qingyun

2017-07-18

Geologic CO 2 sequestration (GCS) is a promising strategy to mitigate anthropogenic CO 2 emission to the atmosphere. Suitable geologic storage sites should have a porous reservoir rock zone where injected CO 2 can displace brine and be stored in pores, and an impermeable zone on top of reservoir rocks to hinder upward movement of buoyant CO 2 . The injection wells (steel casings encased in concrete) pass through these geologic zones and lead CO 2 to the desired zones. In subsurface environments, CO 2 is reactive as both a supercritical (sc) phase and aqueous (aq) species. Its nanoscale chemical reactions with geomedia and wellbores are closely related to the safety and efficiency of CO 2 storage. For example, the injection pressure is determined by the wettability and permeability of geomedia, which can be sensitive to nanoscale mineral-fluid interactions; the sealing safety of the injection sites is affected by the opening and closing of fractures in caprocks and the alteration of wellbore integrity caused by nanoscale chemical reactions; and the time scale for CO 2 mineralization is also largely dependent on the chemical reactivities of the reservoir rocks. Therefore, nanoscale chemical processes can influence the hydrogeological and mechanical properties of geomedia, such as their wettability, permeability, mechanical strength, and fracturing. This Account reviews our group's work on nanoscale chemical reactions and their qualitative impacts on seal integrity and storage capacity at GCS sites from four points of view. First, studies on dissolution of feldspar, an important reservoir rock constituent, and subsequent secondary mineral precipitation are discussed, focusing on the effects of feldspar crystallography, cations, and sulfate anions. Second, interfacial reactions between caprock and brine are introduced using model clay minerals, with focuses on the effects of water chemistries (salinity and organic ligands) and water content on mineral dissolution and

Reaction mechanisms for enhancing carbon dioxide mineral sequestration

Science.gov (United States)

Jarvis, Karalee Ann

Increasing global temperature resulting from the increased release of carbon dioxide into the atmosphere is one of the greatest problems facing society. Nevertheless, coal plants remain the largest source of electrical energy and carbon dioxide gas. For this reason, researchers are searching for methods to reduce carbon dioxide emissions into the atmosphere from the combustion of coal. Mineral sequestration of carbon dioxide reacted in electrolyte solutions at 185°C and 2200 psi with olivine (magnesium silicate) has been shown to produce environmentally benign carbonates. However, to make this method feasible for industrial applications, the reaction rate needs to be increased. Two methods were employed to increase the rate of mineral sequestration: reactant composition and concentration were altered independently in various runs. The products were analyzed with complete combustion for total carbon content. Crystalline phases in the product were analyzed with Debye-Scherrer X-ray powder diffraction. To understand the reaction mechanism, single crystals of San Carlos Olivine were reacted in two solutions: (0.64 M NaHCO3/1 M NaCl) and (5.5 M KHCO3) and analyzed with scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron energy loss spectroscopy (EELS), and fluctuation electron microscopy (FEM) to study the surface morphology, atomic crystalline structure, composition and amorphous structure. From solution chemistry studies, it was found that increasing the activity of the bicarbonate ion increased the conversion rate of carbon dioxide to magnesite. The fastest conversion, 60% conversion in one hour, occurred in a solution of 5.5 M KHCO3. The reaction product particles, magnesium carbonate, significantly increased in both number density and size on the coupon when the bicarbonate ion activity was increased. During some experiments reaction vessel corrosion also altered the mineral sequestration mechanism. Nickel ions from vessel

International Collaboration on CO2 Sequestration

Energy Technology Data Exchange (ETDEWEB)

Peter H. Israelsson; E. Eric Adams

2007-06-30

On December 4, 1997, the US Department of Energy (USDOE), the New Energy and Industrial Technology Development Organization of Japan (NEDO), and the Norwegian Research Council (NRC) entered into a Project Agreement for International Collaboration on CO{sub 2} Ocean Sequestration. Government organizations from Japan, Canada, and Australia, and a Swiss/Swedish engineering firm later joined the agreement, which outlined a research strategy for ocean carbon sequestration via direct injection. The members agreed to an initial field experiment, with the hope that if the initial experiment was successful, there would be subsequent field evaluations of increasingly larger scale to evaluate environmental impacts of sequestration and the potential for commercialization. The evolution of the collaborative effort, the supporting research, and results for the International Collaboration on CO{sub 2} Ocean Sequestration were documented in almost 100 papers and reports, including 18 peer-reviewed journal articles, 46 papers, 28 reports, and 4 graduate theses. These efforts were summarized in our project report issued January 2005 and covering the period August 23, 1998-October 23, 2004. An accompanying CD contained electronic copies of all the papers and reports. This report focuses on results of a two-year sub-task to update an environmental assessment of acute marine impacts resulting from direct ocean sequestration. The approach is based on the work of Auerbach et al. [6] and Caulfield et al. [20] to assess mortality to zooplankton, but uses updated information concerning bioassays, an updated modeling approach and three modified injection scenarios: a point release of negatively buoyant solid CO{sub 2} hydrate particles from a moving ship; a long, bottom-mounted diffuser discharging buoyant liquid CO{sub 2} droplets; and a stationary point release of hydrate particles forming a sinking plume. Results suggest that in particular the first two discharge modes could be

Terrestrial Sequestration of CO2 – An Assessment of Research Needs

Energy Technology Data Exchange (ETDEWEB)

Dove, Patricia [Georgia Inst. of Technology, Atlanta, GA (United States); Richter, Frank [University of Chicago, Chicago, IL; Rudnicki, John W [Northwestern Univ., Evanston, IL (United States); Harris, Jerry [Stanford Univ., CA (United States); Logan, John M. [Logan and Associates, Inc., Bandon, Oregon; Warpinski, Norman R [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Wawersik, Wolfgang R [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Wilson, John L [New Mexico Institute of Mining and Technology; Wong, Teng-Fong [State University of New York; Ortoleva, Peter J [Indiana University, Bloomington, Indiana; Orr, Jr., Franklin M [Stanford Univ., CA (United States); Pyrak-Nolte, Laura [Purdue Univ., West Lafayette, IN (United States)

1998-11-02

Scientific debate about global warming prompted the Office of Basic Energy Sciences (OBES) of the U.S. Department of Energy to assess a broad range of research possibilities that might result in more efficient energy and reduce the amount of greenhouse gases emitted to the atmosphere. Therefore, in May 1998, the Geosciences Research Program of OBES invited eleven panelists to a workshop in order to address the potential for the sequestration of CO2 in geologic formations as part of a possible OBES initiative on climate change technology. Starting with knowledge gained from the industrial use of CO2 for enhanced oil recovery, the panelists were asked to identify the fundamental scientific and technical issues that would enhance the safety, efficiency and predictability of terrestrial CO2 sequestration. This report is the product of the May, 1998 workshop and subsequent discussions among the panelists. Although many of the problems discussed cut across traditional geoscience disciplines, the background of the workshop participants naturally lead to a paper with four sections representing the perspectives of geohydrology, geochemistry, geomechanics, and geophysics.

CO2 sequestration using principles of shell formation

Energy Technology Data Exchange (ETDEWEB)

Lee, Seung-Woo; Jang, Young-Nam [CO2 Sequestration Research Department, Korea Institute of Geoscience and Mineral Resources (Korea, Republic of); Lee, Si-Hyun; Lim, Kyoung-Soo; Jeong, Soon-Kwan [Energy Conservation Research Department of Clean Energy System Research Center, Korea Institute of Energy Research (Korea, Republic of)

2011-06-15

The biomimetic sequestration of carbon dioxide to reduce the CO2 emitted into the atmosphere is introduced in this paper. Bivalve shells are used as a good model of CO2 sequestration in this paper, because the shell is derived from the calcium ions and CO2 in seawater. Carbonic anhydrase, hemocyte from diseased shell (HDS) and extrapallial fluid (EFP) are involved in shell formation. This paper compares the soluble protein extracted from Crassostrea gigas with bovine carbonic anhydrase II in terms of their ability to promote CO2 hydration and the production of calcium precipitates. The result demonstrates that HDS has more functional groups to bind calcium ions in aqueous systems, and a different process of calcium precipitation, than does bovine carbonic anhydrase II. To understand molecular weight and secondary protein structure, mass-spectroscopic analysis (MALDI-TOF) and circular dichroism (CD) analysis were used. With regard to EPF, EPF related to shell formation is composed of several fractions and plays a role in sequestration of CO2.

A simulation method for the rapid screening of potential depleted oil reservoirs for CO2 sequestration

International Nuclear Information System (INIS)

Bossie-Codreanu, D.; Le Gallo, Y.

2004-01-01

The reduction of greenhouse gases emission is a growing concern of many industries. The oil and gas industry has a long commercial practice of gas injection, enhanced oil recovery (EOR) and gas storage. Using a depleted oil or gas reservoir for CO 2 storage has several interesting advantages. The long-term risk analysis of the CO 2 behavior and its impact on the environment is a major concern. That is why the selection of an appropriate reservoir is crucial to the success of a sequestration operation. Our modeling study, based on a synthetic reservoir, quantifies uncertainties due to reservoir parameters in order to establish a set of guidelines to select the most appropriate depleted reservoirs. Several production and sequestration scenarios are investigated in order to quantify key parameter for CO 2 storage. The influence of parameters such as API gravity, heterogeneity (Dykstra-Parson coefficient), pressure support (water injection) and cap rock integrity are analyzed. Estimation of sequestration capacity is proposed through a sequestration factor (SF) estimated for different reservoir production drives. Multiple regression relationships were developed, allowing SF estimation. CO 2 sequestration optimization highlights the best clean oil recovery strategy (CO 2 injection and/or oil production)

Mineral Carbonation Potential of CO2 from Natural and Industrial-based Alkalinity Sources

Science.gov (United States)

Wilcox, J.; Kirchofer, A.

2014-12-01

Mineral carbonation is a Carbon Capture and Storage (CSS) technology where gaseous CO2 is reacted with alkaline materials (such as silicate minerals and alkaline industrial wastes) and converted into stable and environmentally benign carbonate minerals (Metz et al., 2005). Here, we present a holistic, transparent life cycle assessment model of aqueous mineral carbonation built using a hybrid process model and economic input-output life cycle assessment approach. We compared the energy efficiency and the net CO2 storage potential of various mineral carbonation processes based on different feedstock material and process schemes on a consistent basis by determining the energy and material balance of each implementation (Kirchofer et al., 2011). In particular, we evaluated the net CO2 storage potential of aqueous mineral carbonation for serpentine, olivine, cement kiln dust, fly ash, and steel slag across a range of reaction conditions and process parameters. A preliminary systematic investigation of the tradeoffs inherent in mineral carbonation processes was conducted and guidelines for the optimization of the life-cycle energy efficiency are provided. The life-cycle assessment of aqueous mineral carbonation suggests that a variety of alkalinity sources and process configurations are capable of net CO2 reductions. The maximum carbonation efficiency, defined as mass percent of CO2 mitigated per CO2 input, was 83% for CKD at ambient temperature and pressure conditions. In order of decreasing efficiency, the maximum carbonation efficiencies for the other alkalinity sources investigated were: olivine, 66%; SS, 64%; FA, 36%; and serpentine, 13%. For natural alkalinity sources, availability is estimated based on U.S. production rates of a) lime (18 Mt/yr) or b) sand and gravel (760 Mt/yr) (USGS, 2011). The low estimate assumes the maximum sequestration efficiency of the alkalinity source obtained in the current work and the high estimate assumes a sequestration efficiency

Coupled multiphase reactive flow and mineral dissolution-precipitation kinetics: Examples of long-term CO2 sequestration in Utsira Sand, Norway and Mt. Simon Formation, Midwest USA

Science.gov (United States)

Zhang, Y.; Zhang, G.; Lu, P.; Hu, B.; Zhu, C.

2017-12-01

The extent of CO2 mineralization after CO2 injection into deep saline aquifers is a result of the complex coupling of multiphase fluid flow, mass transport, and brine-mineral reactions. The effects of dissolution rate laws and groundwater flow on the long-term fate of CO2 have been seriously overlooked. To investigate these effects, we conducted multiphase (CO2 and brine) coupled reactive transport modeling of CO2 storage in two sandy formations (Utsira Sand, Norway1,2 and Mt. Simon formation, USA 3) using ToughReact and simulated a series of scenarios. The results indicated that: (1) Different dissolution rate laws for feldspars can significantly affect the amount of CO2 mineralization. Increased feldspar dissolution will promote CO2 mineral trapping through the coupling between feldspar dissolution and carbonate mineral precipitation at raised pH. The predicted amount of CO2 mineral trapping when using the principle of detailed balancing-based rate law for feldspar dissolution is about twice as much as that when using sigmoidal rate laws in the literature. (2) Mineral trapping is twice as much when regional groundwater flow is taken into consideration in long-term simulations (e.g., 10,000 years) whereas most modeling studies neglected the regional groundwater flow back and effectively simulated a batch reactor process. Under the influence of regional groundwater flow, the fresh brine from upstream continuously dissolves CO2 at the tail of CO2 plume, generating a large acidified area where large amount of CO2 mineralization takes place. The upstream replenishment of groundwater results in ˜22% mineral trapping at year 10,000, compared to ˜4% when this effect is ignored. Refs: 1Zhang, G., Lu, P., Wei, X., Zhu, C. (2016). Impacts of Mineral Reaction Kinetics and Regional Groundwater Flow on Long-Term CO2 Fate at Sleipner. Energy & Fuels, 30(5), 4159-4180. 2Zhu, C., Zhang, G., Lu, P., Meng, L., Ji, X. (2015). Benchmark modeling of the Sleipner CO2 plume

Enhanced coal bed methane production and sequestration of CO₂ in unmineable coal

Energy Technology Data Exchange (ETDEWEB)

Locke, James [CONSOL Energy Inc., South Park, PA (United States); Winschel, Richard [CONSOL Energy Inc., South Park, PA (United States)

2005-03-01

The Marshall County Project was undertaken by CONSOL Energy Inc. (CONSOL) with partial funding from the U. S. Department of Energy’s (DOE) Carbon Storage Program (CSP). The project, initiated in October 2001, was conducted to evaluate opportunities for carbon dioxide CO2 sequestration in an unmineable coal seam in the Northern Appalachian Basin with simultaneous enhanced coal bed methane recovery. This report details the final results from the project that established a pilot test in Marshall County, West Virginia, USA, where a series of coal bed methane (CBM) production wells were developed in an unmineable coal seam (Upper Freeport (UF)) and the overlying mineable Pittsburgh (PIT) seam. The initial wells were drilled beginning in 2003, using slant-hole drilling procedures with a single production leg, in a down-dip orientation that provided limited success. Improved well design, implemented in the remaining wells, allowed for greater CBM production. The nearly-square-shaped project area was bounded by the perimeter production wells in the UF and PIT seams encompassing an area of 206 acres. Two CBM wells were drilled into the UF at the center of the project site, and these were later converted to serve as CO2 injection wells through which, 20,000 short tons of CO2 were planned to be injected at a maximum rate of 27 tons per day. A CO2 injection system comprised of a 50-ton liquid CO2 storage tank, a cryogenic pump, and vaporization system was installed in the center of the site and, after obtaining a Class II underground injection permit (UIC) permit from the West Virginia Department of Environmental Protection (WVDEP), CO2 injection, through the two center wells, into the UF was initiated in September 2009. Numerous complications limited CO2 injection continuity, but CO2 was injected until breakthrough was encountered in September 2013, at which point the project had achieved an injection total of 4,968 tons of CO2. During the injection and post

Regulating forest rotation to increase CO{sub 2} sequestration

Energy Technology Data Exchange (ETDEWEB)

Gong, P.; Kristroem, B.

1999-06-01

Previous studies have shown that the optimal forest rotation age increases considerably if the benefits of CO{sub 2} sequestration are included in rotation decisions. While these studies provide some guidelines for managing public forests, private forest owners may not choose the socially optimal rotation age. This paper discusses a regulation measure to increase CO{sub 2} sequestration in privately owned forests. The regulation problem is treated as a sequential game, where the regulator chooses a subsidy scheme and forest owners respond by changing rotation ages. A private forest owner receives a subsidy at the time of harvesting if he/she changes the rotation age towards the socially optimal one. The subsidy is proportional to the associated change in timber yield. The forest owner`s objective is to maximize the net present value of after-tax timber production profits and subsidies. The regulator`s decision problem is to find the subsidy rate that maximizes the net benefits of implementing the policy (the net of increased CO{sub 2} sequestration benefits, subsidy costs, and changes in forestry taxation income). Empirical results for Swedish examples show that the optimal subsidy rate is sensitive to the marginal benefit of CO{sub 2} sequestration, the social discount rate, and site quality. The optimal subsidy rate is found to be significantly lower than the marginal benefit of CO{sub 2} sequestration. With the proposed subsidy scheme, private forest owners will choose rotation ages longer than the Faustmann rotation, but significantly shorter than the socially optimal rotation age 21 refs, 6 tabs. Arbetsrapport 272

Integrated Mid-Continent Carbon Capture, Sequestration & Enhanced Oil Recovery Project

Energy Technology Data Exchange (ETDEWEB)

Brian McPherson

2010-08-31

A consortium of research partners led by the Southwest Regional Partnership on Carbon Sequestration and industry partners, including CAP CO2 LLC, Blue Source LLC, Coffeyville Resources, Nitrogen Fertilizers LLC, Ash Grove Cement Company, Kansas Ethanol LLC, Headwaters Clean Carbon Services, Black & Veatch, and Schlumberger Carbon Services, conducted a feasibility study of a large-scale CCS commercialization project that included large-scale CO{sub 2} sources. The overall objective of this project, entitled the 'Integrated Mid-Continent Carbon Capture, Sequestration and Enhanced Oil Recovery Project' was to design an integrated system of US mid-continent industrial CO{sub 2} sources with CO{sub 2} capture, and geologic sequestration in deep saline formations and in oil field reservoirs with concomitant EOR. Findings of this project suggest that deep saline sequestration in the mid-continent region is not feasible without major financial incentives, such as tax credits or otherwise, that do not exist at this time. However, results of the analysis suggest that enhanced oil recovery with carbon sequestration is indeed feasible and practical for specific types of geologic settings in the Midwestern U.S.

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.

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.

CO{sub 2} sequestration technologies

Energy Technology Data Exchange (ETDEWEB)

Ketzer, Marcelo [Brazilian Carbon Storage Research Center (Brazil)

2008-07-15

In this presentation the importance of the capture and sequestration of CO{sub 2} is outlined for the reduction of gas discharges of greenhouse effect; then the principles of CO{sub 2} storage in geologic formations are reviewed; afterwards, the analogs for the CO{sub 2} storage are commented, such as the storage of the acid gas, the natural gas storage and the natural CO{sub 2} deposits. Also it is spoken on the CO{sub 2} storage in coal, in water-bearing saline deposits and in oil fields, and finally the subject of the safety and monitoring of the CO{sub 2} storage is reviewed. [Spanish] En esta presentacion se expone la importancia de la captura y secuestro de CO{sub 2} para la reduccion de emisiones de gases de efecto invernadero; luego se tratan los principios de almacenamiento de CO{sub 2} en formaciones geologicas; despues se comentan los analogos para el almacenamiento de CO{sub 2} como el almacenamiento del gas acido, el almacenamiento de gas natural y los yacimientos naturales de CO{sub 2}. Tambien se habla sobre el almacenamiento de CO{sub 2} en carbon, acuiferos salinos y yacimientos petroliferos y por ultimo se toca el tema de la seguridad y monitoreo del almacenamiento de CO{sub 2}.

Potential Hydrogeomechanical Impacts of Geological CO2 Sequestration

Science.gov (United States)

McPherson, B. J.; Haerer, D.; Han, W.; Heath, J.; Morse, J.

2006-12-01

Long-term sequestration of anthropogenic "greenhouse gases" such as CO2 is a proposed approach to managing climate change. Deep brine reservoirs in sedimentary basins are possible sites for sequestration, given their ubiquitous nature. We used a mathematical sedimentary basin model, including coupling of multiphase CO2-groundwater flow and rock deformation, to evaluate residence times in possible brine reservoir storage sites, migration patterns and rates away from such sites, and effects of CO2 injection on fluid pressures and rock strain. Study areas include the Uinta and Paradox basins of Utah, the San Juan basin of New Mexico, and the Permian basin of west Texas. Regional-scale hydrologic and mechanical properties, including the presence of fracture zones, were calibrated using laboratory and field data. Our initial results suggest that, in general, long-term (~100 years or more) sequestration in deep brine reservoirs is possible, if guided by robust structural and hydrologic data. However, specific processes must be addressed to characterize and minimize risks. In addition to CO2 migration from target sequestration reservoirs into other reservoirs or to the land surface, another environmental issue is displacement of brines into freshwater aquifers. We evaluated the potential for such unintended aquifer contamination by displacement of brines out of adjacent sealing layers such as marine shales. Results suggest that sustained injection of CO2 may incur significant brine displacement out of adjacent sealing layers, depending on the injection history, initial brine composition, and hydrologic properties of both reservoirs and seals. Model simulations also suggest that as injection-induced overpressures migrate, effective stresses may follow this migration under some conditions, as will associated rock strain. Such "strain migration" may lead to induced or reactivated fractures or faults, but can be controlled through reservoir engineering.

INTERNATIONAL COLLABORATION ON CO2 SEQUESTRATION

Energy Technology Data Exchange (ETDEWEB)

H.J. Herzog; E.E. Adams

2000-08-23

The specific objective of our project on CO{sub 2} ocean sequestration is to investigate its technical feasibility and to improve the understanding of any associated environmental impacts. Our ultimate goal is to minimize any impacts associated with the eventual use of ocean carbon sequestration to reduce greenhouse gas concentrations in the atmosphere. The project will continue through March 31, 2002, with a field experiment to take place in the summer of 2001 off the Kona Coast of Hawaii. At GHGT-4 in Interlaken, we presented a paper detailing our plans. The purpose of this paper is to present an update on our progress to date and our plans to complete the project. The co-authors of this paper are members of the project's Technical Committee, which has been formed to supervise the technical aspects and execution of this project.

Biologically Enhanced Carbon Sequestration: Research Needs and Opportunities

Energy Technology Data Exchange (ETDEWEB)

Oldenburg, Curtis; Oldenburg, Curtis M.; Torn, Margaret S.

2008-03-21

Fossil fuel combustion, deforestation, and biomass burning are the dominant contributors to increasing atmospheric carbon dioxide (CO{sub 2}) concentrations and global warming. Many approaches to mitigating CO{sub 2} emissions are being pursued, and among the most promising are terrestrial and geologic carbon sequestration. Recent advances in ecology and microbial biology offer promising new possibilities for enhancing terrestrial and geologic carbon sequestration. A workshop was held October 29, 2007, at Lawrence Berkeley National Laboratory (LBNL) on Biologically Enhanced Carbon Sequestration (BECS). The workshop participants (approximately 30 scientists from California, Illinois, Oregon, Montana, and New Mexico) developed a prioritized list of research needed to make progress in the development of biological enhancements to improve terrestrial and geologic carbon sequestration. The workshop participants also identified a number of areas of supporting science that are critical to making progress in the fundamental research areas. The purpose of this position paper is to summarize and elaborate upon the findings of the workshop. The paper considers terrestrial and geologic carbon sequestration separately. First, we present a summary in outline form of the research roadmaps for terrestrial and geologic BECS. This outline is elaborated upon in the narrative sections that follow. The narrative sections start with the focused research priorities in each area followed by critical supporting science for biological enhancements as prioritized during the workshop. Finally, Table 1 summarizes the potential significance or 'materiality' of advances in these areas for reducing net greenhouse gas emissions.

Experiments and geochemical modelling of CO{sub 2} sequestration by olivine: Potential, quantification

Energy Technology Data Exchange (ETDEWEB)

Garcia, B., E-mail: Bruno.Garcia@ifp.fr [Institut Francais du Petrole, 1 et 4 Avenue du Bois Preau, 92852 Rueil Malmaison (France); Beaumont, V.; Perfetti, E.; Rouchon, V.; Blanchet, D. [Institut Francais du Petrole, 1 et 4 Avenue du Bois Preau, 92852 Rueil Malmaison (France); Oger, P.; Dromart, G. [Universite de Lyon, CNRS, UMR 5570, ENS de Lyon, Site Monod, 15 Parvis Rene Descartes BP 7000, Lyon F-69342 (France); Huc, A.-Y.; Haeseler, F. [Institut Francais du Petrole, 1 et 4 Avenue du Bois Preau, 92852 Rueil Malmaison (France)

2010-09-15

Aqueous solutions equilibrated with supercritical CO{sub 2} (150 deg. C and total pressure of 150 bar) were investigated in order to characterize their respective conditions of carbonation. Dissolution of olivine and subsequent precipitation of magnesite with a net consumption of CO{sub 2} were expected. A quantified pure mineral phase (powders with different olivine grain diameter [20-80 {mu}m], [80-125 {mu}m], [125-200 {mu}m] and [>200 {mu}m]), and CO{sub 2} (as dried ice) were placed in closed-batch reactors (soft Au tubes) in the presence of solutions. Different salinities (from 0 to 3400 mM) and different ratios of solution/solid (mineral phase) (from 0.1 to 10) were investigated. Experiments were performed over periods from 2 to 8 weeks. Final solid products were quantified by the Rock-Eval 6 technique, and identified using X-ray diffraction, Raman spectroscopy, electron microprobe and scanning electron microscopy. Gaseous compounds were quantified by a vacuum line equipped with a Toepler pump and identified and measured by gas chromatography (GC). Carbon mass balances were calculated. Olivine reacted completely with CO{sub 2}, trapping up to 57 {+-} 2% (eqC of initial CO{sub 2}) as magnesite; some amorphous silica also formed. Olivine grain diameter and solution/mineral ratios appeared to be the primary controls on the reaction, salinity acting as a second order parameter. During the experiments, fluid analyses may not be performed with approach adopted but, geochemical modelling was attempted to give information about the solution composition. This showed an interesting mineral matrix evolution. Under the experimental conditions, olivine appeared to be a good candidate for CO{sub 2} trapping into a geologically stable carbonate, magnesite. The possible use of mafic and ultramafic rocks for CO{sub 2} sequestration is discussed.

Reduction of the greenhouse effect by geological mineral in-situ sequestration of CO{sub 2} in basic rocks: bibliographic synthesis and possibilities in France. Final report; Reduction de l'effet de serre par sequestration geologique minerale in-situ de CO{sub 2} au sein de roches basiques: synthese bibliographique et revue des potentialites en France. Rapport final

Energy Technology Data Exchange (ETDEWEB)

Marechal, J.C.; Lachassagne, P

2004-07-01

The report constitutes a first bibliographic study defining the environments the most adapted to the geological mineral in-situ sequestration of CO{sub 2}. For each environment the lithology and the rocks permeability and porosity are analyzed. Thus the possible rocks and deposits in France are presented. (A.L.B.)

Evaluation of Southern Quebec asbestos residues for CO2 sequestration by mineral carbonation

Energy Technology Data Exchange (ETDEWEB)

Beaudoin, G.; Hebert, R.; Constantin, M. [Laval Univ., Quebec City, PQ (Canada); Bonin, G. [LAB Chrysotile Inc., Black Lake, PQ (Canada); Dipple, G. [British Columbia Univ., Vancouver, BC (Canada)

2003-08-01

One alternative to help reduce carbon dioxide (CO{sub 2}) levels in the atmosphere is to sequester CO{sub 2} by mineral carbonation using ultramafic rock-hosted magnesian silicates (serpentine, olivine, talc). The carbonation process produces magnesite, which is a geologically stable and an environmentally safe magnesium carbonate. Three CO{sub 2} sinks exist in southern Quebec use such silicates. They are: (1) asbestos mill residues, (2) associated mine waste, and (3) ultramafic bedrock. Extraction of asbestos in the region has been accomplished from serpentinized harzburgite located in the Thetford Mines and Asbestos ophiolitic massifs and also from the highly sheared Pennington Sheet. The physical and chemical properties of magnesium silicate deposits greatly determine their carbonation potential. A wide range of properties was observed in samples obtained from almost all asbestos mill residues and waste. The reaction which takes place depends on the mineral content. The kinetics of the reactions are influenced by humidity and grain size.

CO2 geological sequestration: state of art in Italy and abroad

International Nuclear Information System (INIS)

Quattrocchi, Fedora; Bencini, Roberto

2005-01-01

This paper proposes a wide scenario on the state of art in Italy and abroad of industrial CO 2 geological sequestration, with particular attention to Weyburn Project. Geochemical monitoring techniques are described, mentioning also geophysical monitoring techniques for CO 2 injected into the soil. Critical choices and objections in Italy to a complete use of clean fossil fuels, hydrogen carrier, clean coal technologies: all of these approaches require geological sequestration of CO 2 [it

Carbon dioxide sequestration induced mineral precipitation healing of fractured reservoir seals

Science.gov (United States)

Welch, N.; Crawshaw, J.

2017-12-01

Initial experiments and the thermodynaic basis for carbon dioxide sequestration induced mineral precipitation healing of fractures through reservoir seals will be presented. The basis of this work is the potential exists for the dissolution of reservoir host rock formation carbonate minerals in the acidified injection front of CO2 during sequestration or EOR. This enriched brine and the bulk CO2 phase will then flow through the reservoir until contact with the reservoir seal. At this point any fractures present in the reservoir seal will be the preferential flow path for the bulk CO2 phase as well as the acidified brine front. These fractures would currently be filled with non-acidified brine saturated in seal formation brine. When the acidifeid brine from the host formation and the cap rock brine mix there is the potential for minerals to fall out of solution, and for these precipitated minerals to decrease or entirely cut off the fluid flow through the fractures present in a reservoir seal. Initial equilibrium simulations performed using the PHREEQC1 database drived from the PHREEQE2 database are used to show the favorable conditions under which this mineral precipitation can occurs. Bench scale fluid mixing experiments were then performed to determine the kinetics of the mineral precipitation process, and determine the progress of future experiemnts involving fluid flow within fractured anhydrite reservoir seal samples. 1Parkhurst, D.L., and Appelo, C.A.J., 2013, Description of input and examples for PHREEQC version 3—A computer program for speciation, batch-reaction, one-dimensional transport, and inverse geochemical calculations: U.S. Geological Survey Techniques and Methods, book 6, chap. A43, 497 p., available only at https://pubs.usgs.gov/tm/06/a43/. 2Parkhurst, David L., Donald C. Thorstenson, and L. Niel Plummer. PHREEQE: a computer program for geochemical calculations. No. 80-96. US Geological Survey, Water Resources Division,, 1980.

CO2, the promises of geological sequestration

International Nuclear Information System (INIS)

Rouat, S.

2006-01-01

Trapping part of the world CO 2 effluents in the deep underground is a profitable and ecological way to limit the global warming. This digest paper presents the different ways of CO 2 sequestration (depleted oil and gas fields, unexploited coal seams, saline aquifers), the other possible solutions for CO 2 abatement (injection in the bottom of the ocean, conversion into carbonates by injection into basic rocks, fixation by photosynthesis thanks to micro-algae cultivation), and takes stock of the experiments in progress (Snoehvit field in Norway, European project Castor). (J.S.)

A Novel Approach To Mineral Carbonation: Enhancing Carbonation While Avoiding Mineral Pretreatment Process Cost

Energy Technology Data Exchange (ETDEWEB)

Michael J. McKelvy; Andrew V. G. Chizmeshya; Kyle Squires; Ray W. Carpenter; Hamdallah Bearat

2006-06-21

Known fossil fuel reserves, especially coal, can support global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other CO{sub 2} sequestration candidate technologies that propose long-term storage, mineral sequestration provides permanent disposal by forming geologically stable mineral carbonates. Carbonation of the widely occurring mineral olivine (e.g., forsterite, Mg{sub 2}SiO{sub 4}) is a large-scale sequestration process candidate for regional implementation, which converts CO{sub 2} into the environmentally benign mineral magnesite (MgCO{sub 3}). The primary goal is cost-competitive process development. As the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is key to economic viability. Recent studies at the U.S. DOE Albany Research Center have established that aqueous-solution carbonation using supercritical CO{sub 2} is a promising process; even without olivine activation, 30-50% carbonation has been achieved in an hour. Mechanical activation (e.g., attrition) has accelerated the carbonation process to an industrial timescale (i.e., near completion in less than an hour), at reduced pressure and temperature. However, the activation cost is too high to be economical and lower cost pretreatment options are needed. Herein, we report our second year progress in exploring a novel approach that offers the potential to substantially enhance carbonation reactivity while bypassing pretreatment activation. As our second year progress is intimately related to our earlier work, the report is presented in that context to provide better overall understanding of the progress made. We have discovered that robust silica-rich passivating layers form on the olivine surface during carbonation. As carbonation proceeds, these passivating layers thicken, fracture and eventually exfoliate, exposing fresh olivine surfaces during rapidly

An experimental study on mineral sequestration of CO2 in basics and ultra basics rocks

International Nuclear Information System (INIS)

Dufaud, F.

2006-11-01

The first part of the thesis is dedicated to dissolution data of siderite FeCO 3 and magnetite Fe 3 O 4 which have been monitored in situ on the FAME beamline of the european synchrotron radiation facility in Grenoble. Iron in solution close to siderite single crystals is shown to be divalent hydrated. The small size of the experimentally investigated volume of solution (200 *400 micrometer and 3 mm height) allowed to work with single crystals in well defined geometries. No specific interaction was observed between iron (II) and dissolved inorganic carbon, suggesting that modelling siderite evolution under high CO 2 pressures by using CO 2 -less very acidic (pH 1-2) solutions is adequate. Using initial reaction rates, we get an activation energy for siderite dissolution of 62 kJ.mol -1 , consistent with existing literature data. Such a value is suggestive of a mineral/solution interface mechanism.. Data from this study and from literature are consistent over a temperature range 25 C - 125 C and a pH range pH 1-7 with an empirical law: pk = pH + E a /(ln(10)*RT(K)) - log(S/V) - 10,5 where E a = 62 kJ.mol -1 and S/V is the ratio between solid surface S and fluid volume V. A value of activation energy of 73.5 kJ.mol -1 is obtained in the case of magnetite, also consistent with mineral/solution processes. The second and major part of the thesis work is the realization of analogical experiments for simulating carbonation of basic and ultra basic minerals. Experiments were carried out on consolidated rock cores at 90 C and 280 bar of CO 2 (low temperature experiments) and on powders contained in metallic capsules at 400-500 C and 1000-1700 bars of CO 2 (high temperature experiments). The rate of mineral storage of CO 2 was defined as the molar ratio of solid carbonate formed over total CO 2 injected. It is of about 1% in three months in low temperature experiments whereas it reaches several tens of percents per hour in high temperature experiments. In all cases

FEASIBILITY OF LARGE-SCALE OCEAN CO2 SEQUESTRATION

Energy Technology Data Exchange (ETDEWEB)

Dr. Peter Brewer; Dr. James Barry

2002-09-30

We have continued to carry out creative small-scale experiments in the deep ocean to investigate the science underlying questions of possible future large-scale deep-ocean CO{sub 2} sequestration as a means of ameliorating greenhouse gas growth rates in the atmosphere. This project is closely linked to additional research funded by the DoE Office of Science, and to support from the Monterey Bay Aquarium Research Institute. The listing of project achievements here over the past year reflects these combined resources. Within the last project year we have: (1) Published a significant workshop report (58 pages) entitled ''Direct Ocean Sequestration Expert's Workshop'', based upon a meeting held at MBARI in 2001. The report is available both in hard copy, and on the NETL web site. (2) Carried out three major, deep ocean, (3600m) cruises to examine the physical chemistry, and biological consequences, of several liter quantities released on the ocean floor. (3) Carried out two successful short cruises in collaboration with Dr. Izuo Aya and colleagues (NMRI, Osaka, Japan) to examine the fate of cold (-55 C) CO{sub 2} released at relatively shallow ocean depth. (4) Carried out two short cruises in collaboration with Dr. Costas Tsouris, ORNL, to field test an injection nozzle designed to transform liquid CO{sub 2} into a hydrate slurry at {approx}1000m depth. (5) In collaboration with Prof. Jill Pasteris (Washington University) we have successfully accomplished the first field test of a deep ocean laser Raman spectrometer for probing in situ the physical chemistry of the CO{sub 2} system. (6) Submitted the first major paper on biological impacts as determined from our field studies. (7) Submitted a paper on our measurements of the fate of a rising stream of liquid CO{sub 2} droplets to Environmental Science & Technology. (8) Have had accepted for publication in Eos the first brief account of the laser Raman spectrometer success. (9) Have had two

GEOLOGIC SCREENING CRITERIA FOR SEQUESTRATION OF CO2 IN COAL: QUANTIFYING POTENTIAL OF THE BLACK WARRIOR COALBED METHANE FAIRWAY, ALABAMA

Energy Technology Data Exchange (ETDEWEB)

Jack C. Pashin; Richard E. Carroll; Richard H. Groshong Jr.; Dorothy E. Raymond; Marcella McIntyre; J. Wayne Payton

2004-01-01

Sequestration of CO{sub 2} in coal has potential benefits for reducing greenhouse gas emissions from the highly industrialized Carboniferous coal basins of North America and Europe and for enhancing coalbed methane recovery. Hence, enhanced coalbed methane recovery operations provide a basis for a market-based environmental solution in which the cost of sequestration is offset by the production and sale of natural gas. The Black Warrior foreland basin of west-central Alabama contains the only mature coalbed methane production fairway in eastern North America, and data from this basin provide an excellent basis for quantifying the carbon sequestration potential of coal and for identifying the geologic screening criteria required to select sites for the demonstration and commercialization of carbon sequestration technology. Coalbed methane reservoirs in the upper Pottsville Formation of the Black Warrior basin are extremely heterogeneous, and this heterogeneity must be considered to screen areas for the application of CO{sub 2} sequestration and enhanced coalbed methane recovery technology. Major screening factors include stratigraphy, geologic structure, geothermics, hydrogeology, coal quality, sorption capacity, technology, and infrastructure. Applying the screening model to the Black Warrior basin indicates that geologic structure, water chemistry, and the distribution of coal mines and reserves are the principal determinants of where CO{sub 2} can be sequestered. By comparison, coal thickness, temperature-pressure conditions, and coal quality are the key determinants of sequestration capacity and unswept coalbed methane resources. Results of this investigation indicate that the potential for CO{sub 2} sequestration and enhanced coalbed methane recovery in the Black Warrior basin is substantial and can result in significant reduction of greenhouse gas emissions while increasing natural gas reserves. Coal-fired power plants serving the Black Warrior basin in

Making carbon sequestration a paying proposition

Science.gov (United States)

Han, Fengxiang X.; Lindner, Jeff S.; Wang, Chuji

2007-03-01

Atmospheric carbon dioxide (CO2) has increased from a preindustrial concentration of about 280 ppm to about 367 ppm at present. The increase has closely followed the increase in CO2 emissions from the use of fossil fuels. Global warming caused by increasing amounts of greenhouse gases in the atmosphere is the major environmental challenge for the 21st century. Reducing worldwide emissions of CO2 requires multiple mitigation pathways, including reductions in energy consumption, more efficient use of available energy, the application of renewable energy sources, and sequestration. Sequestration is a major tool for managing carbon emissions. In a majority of cases CO2 is viewed as waste to be disposed; however, with advanced technology, carbon sequestration can become a value-added proposition. There are a number of potential opportunities that render sequestration economically viable. In this study, we review these most economically promising opportunities and pathways of carbon sequestration, including reforestation, best agricultural production, housing and furniture, enhanced oil recovery, coalbed methane (CBM), and CO2 hydrates. Many of these terrestrial and geological sequestration opportunities are expected to provide a direct economic benefit over that obtained by merely reducing the atmospheric CO2 loading. Sequestration opportunities in 11 states of the Southeast and South Central United States are discussed. Among the most promising methods for the region include reforestation and CBM. The annual forest carbon sink in this region is estimated to be 76 Tg C/year, which would amount to an expenditure of 11.1-13.9 billion/year. Best management practices could enhance carbon sequestration by 53.9 Tg C/year, accounting for 9.3% of current total annual regional greenhouse gas emission in the next 20 years. Annual carbon storage in housing, furniture, and other wood products in 1998 was estimated to be 13.9 Tg C in the region. Other sequestration options

Carbon Dioxide Transport and Sorption Behavior in Confined Coal Cores for Enhanced Coalbed Methane and CO2 Sequestration

Energy Technology Data Exchange (ETDEWEB)

Jikich, S.A.; McLendon, T.R.; Seshadri, K.S.; Irdi, G.A.; Smith, D.H.

2007-11-01

Measurements of sorption isotherms and transport properties of CO2 in coal cores are important for designing enhanced coalbed methane/CO2 sequestration field projects. Sorption isotherms measured in the lab can provide the upper limit on the amount of CO2 that might be sorbed in these projects. Because sequestration sites will most likely be in unmineable coals, many of the coals will be deep and under considerable lithostatic and hydrostatic pressures. These lithostatic pressures may significantly reduce the sorption capacities and/or transport rates. Consequently, we have studied apparent sorption and diffusion in a coal core under confining pressure. A core from the important bituminous coal Pittsburgh #8 was kept under a constant, three-dimensional external stress; the sample was scanned by X-ray computer tomography (CT) before, then while it sorbed, CO2. Increases in sample density due to sorption were calculated from the CT images. Moreover, density distributions for small volume elements inside the core were calculated and analyzed. Qualitatively, the computerized tomography showed that gas sorption advanced at different rates in different regions of the core, and that diffusion and sorption progressed slowly. The amounts of CO2 sorbed were plotted vs. position (at fixed times) and vs. time (for various locations in the sample). The resulting sorption isotherms were compared to isotherms obtained from powdered coal from the same Pittsburgh #8 extended sample. The results showed that for this single coal at specified times, the apparent sorption isotherms were dependent on position of the volume element in the core and the distance from the CO2 source. Also, the calculated isotherms showed that less CO2 was sorbed than by a powdered (and unconfined) sample of the coal. Changes in density distributions during the experiment were also observed. After desorption, the density distribution of calculated volume elements differed from the initial distribution

CO2 emissions abatement and geologic sequestration - industrial innovations and stakes - status of researches in progress

International Nuclear Information System (INIS)

2005-01-01

This colloquium was jointly organized by the French institute of petroleum (IFP), the French agency of environmental and energy mastery (Ademe) and the geological and mining research office (BRGM). This press kit makes a status of the advances made in CO 2 emissions abatement and geological sequestration: technological advances of CO 2 capture and sequestration, geological reservoir dimensioning with respect to the problem scale, duration of such an interim solution, CO 2 emissions abatement potentialities of geological sequestration, regulatory, economical and financial implications, international stakes of greenhouse gas emissions. This press kit comprises a press release about the IFP-Ademe-BRGM colloquium, a slide presentation about CO 2 abatement and sequestration, and four papers: a joint IFP-Ademe-BRGM press conference, IFP's answers to CO 2 emissions abatement, Ademe's actions in CO 2 abatement and sequestration, and BRGM's experience in CO 2 sequestration and climatic change expertise. (J.S.)

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.

Making carbon dioxide sequestration feasible: Toward federal regulation of CO2 sequestration pipelines

International Nuclear Information System (INIS)

Mack, Joel; Endemann, Buck

2010-01-01

As the United States moves closer to a national climate change policy, it will have to focus on a variety of factors affecting the manner in which the country moves toward a future with a substantially lower carbon footprint. In addition to encouraging renewable energy, smart grid, clean fuels and other technologies, the United States will need to make substantial infrastructure investments in a variety of industries. Among the significant contributors to the current carbon footprint in the United States is the use of coal as a major fuel for the generation of electricity. One of the most important technologies that the United States can employ to reduce its carbon footprint is to sequester the carbon dioxide ('CO 2 ') from coal-fired power plants. This article focuses on the legal and policy issues surrounding a critical piece of the necessary sequestration infrastructure: CO 2 pipelines that will carry CO 2 from where it is removed from fuel or waste gas streams to where it will be sequestered. Ultimately, this article recommends developing a federally regulated CO 2 pipeline program to foster the implementation of carbon sequestration technology.

Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

Energy Technology Data Exchange (ETDEWEB)

O' Connor, W.K.; Dahlin, D.C.; Nilsen, D.N.; Walters, R.P.; Turner, P.C.

2000-07-01

The Albany Research Center (ARC) of the US Department of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite and member (mg{sub 2}SiO{sub 4})], or serpentine [Mg{sub 3}Si{sub 2}O{sub 5}(OH){sub 4}]. This slurry is reacted with supercritical carbon dioxide (CO{sub 2}) to produce magnesite (MgCO{sub 3}). The CO{sub 2} is dissolved in water to form carbonic acid (H{sub 2}CO{sub 3}), which dissociates to H{sup +} and HCO{sub 3}{sup {minus}}. The H{sup +} reacts with the mineral, liberating Mg{sup 2+} cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO{sub 2} pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185 C and a partial pressure of CO{sub 2} (P{sub CO{sub 2}}) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction conditions, have achieved roughly 83% conversion of heat treated serpentine

Experimental investigation of geochemical and mineralogical effects of CO2 sequestration on flow characteristics of reservoir rock in deep saline aquifers

Science.gov (United States)

Rathnaweera, T. D.; Ranjith, P. G.; Perera, M. S. A.

2016-01-01

Interactions between injected CO2, brine, and rock during CO2 sequestration in deep saline aquifers alter their natural hydro-mechanical properties, affecting the safety, and efficiency of the sequestration process. This study aims to identify such interaction-induced mineralogical changes in aquifers, and in particular their impact on the reservoir rock’s flow characteristics. Sandstone samples were first exposed for 1.5 years to a mixture of brine and super-critical CO2 (scCO2), then tested to determine their altered geochemical and mineralogical properties. Changes caused uniquely by CO2 were identified by comparison with samples exposed over a similar period to either plain brine or brine saturated with N2. The results show that long-term reaction with CO2 causes a significant pH drop in the saline pore fluid, clearly due to carbonic acid (as dissolved CO2) in the brine. Free H+ ions released into the pore fluid alter the mineralogical structure of the rock formation, through the dissolution of minerals such as calcite, siderite, barite, and quartz. Long-term CO2 injection also creates a significant CO2 drying-out effect and crystals of salt (NaCl) precipitate in the system, further changing the pore structure. Such mineralogical alterations significantly affect the saline aquifer’s permeability, with important practical consequences for the sequestration process. PMID:26785912

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.)

Experiment and simulation study on the effects of cement minerals on the water-rock-CO2 interaction during CO2 geological storage

Science.gov (United States)

Liu, N.; Cheng, J.

2016-12-01

storage and its effects on the CO2-water-rock interaction should be focused no matter for the benefit of injection sustainability or carbon sequestration capability. And more cement minerals such as ankerite should be included and the reservoir quality changes should also be taken consideration in the further study.

A Novel Approach to Mineral Carbonation: Enhancing Carbonation While Avoiding Mineral Pretreatment Process Cost

Energy Technology Data Exchange (ETDEWEB)

Andrew V. G. Chizmeshya; Michael J. McKelvy; Kyle Squires; Ray W. Carpenter; Hamdallah Bearat

2007-06-21

Known fossil fuel reserves, especially coal, can support global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other CO{sub 2} sequestration candidate technologies that propose long-term storage, mineral sequestration provides permanent disposal by forming geologically stable mineral carbonates. Carbonation of the widely occurring mineral olivine (e.g., forsterite, Mg{sub 2}SiO{sub 4}) is a large-scale sequestration process candidate for regional implementation, which converts CO{sub 2} into the environmentally benign mineral magnesite (MgCO{sub 3}). The primary goal is cost-competitive process development. As the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is key to economic viability. Recent studies at the U.S. DOE Albany Research Center have established that aqueous-solution carbonation using supercritical CO{sub 2} is a promising process; even without olivine activation, 30-50% carbonation has been achieved in an hour. Mechanical activation (e.g., attrition) has accelerated the carbonation process to an industrial timescale (i.e., near completion in less than an hour), at reduced pressure and temperature. However, the activation cost is too high to be economical and lower cost pretreatment options are needed. We have discovered that robust silica-rich passivating layers form on the olivine surface during carbonation. As carbonation proceeds, these passivating layers thicken, fracture and eventually exfoliate, exposing fresh olivine surfaces during rapidly-stirred/circulating carbonation. We are exploring the mechanisms that govern carbonation reactivity and the impact that (1) modeling/controlling the slurry fluid-flow conditions, (2) varying the aqueous ion species/size and concentration (e.g., Li+, Na+, K+, Rb+, Cl-, HCO{sub 3}{sup -}), and (3) incorporating select sonication offer to enhance exfoliation and carbonation. Thus

Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

Energy Technology Data Exchange (ETDEWEB)

O' Connor, William K.; Dahlin, David C.; Nilsen, David N.; Walters, Richard P.; Turner, Paul C.

2000-01-01

The Albany Research Center (ARC) of the U.S. Dept. of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. Other participants in this Program include the Los Alamos National Laboratory, Arizona State University, Science Applications International Corporation, and the DOE National Energy Technology Laboratory. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite end member (Mg2SiO4)], or serpentine [Mg3Si2O5(OH)4]. This slurry is reacted with supercritical carbon dioxide (CO2) to produce magnesite (MgCO3). The CO2 is dissolved in water to form carbonic acid (H2CO3), which dissociates to H+ and HCO3 -. The H+ reacts with the mineral, liberating Mg2+ cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO2 pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185?C and a partial pressure of CO2 (PCO2) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction

Preliminary reactive geochemical transport simulation study on CO2 geological sequestration at the Changhua Coastal Industrial Park Site, Taiwan

Science.gov (United States)

Sung, R.; Li, M.

2013-12-01

Mineral trapping by precipitated carbonate minerals is one of critical mechanisms for successful long-term geological sequestration (CGS) in deep saline aquifer. Aquifer acidification induced by the increase of carbonic acid (H2CO3) and bicarbonate ions (HCO3-) as the dissolution of injected CO2 may induce the dissolution of minerals and hinder the effectiveness of cap rock causing potential risk of CO2 leakage. Numerical assessments require capabilities to simulate complicated interactions of thermal, hydrological, geochemical multiphase processes. In this study, we utilized TOUGHREACT model to demonstrate a series of CGS simulations and assessments of (1) time evolution of aquifer responses, (2) migration distance and spatial distribution of CO2 plume, (3) effects of CO2-saline-mineral interactions, and (4) CO2 trapping components at the Changhua Costal Industrial Park (CCIP) Site, Taiwan. The CCIP Site is located at the Southern Taishi Basin with sloping and layered heterogeneous formations. At this preliminary phase, detailed information of mineralogical composition of reservoir formation and chemical composition of formation water are difficult to obtain. Mineralogical composition of sedimentary rocks and chemical compositions of formation water for CGS in deep saline aquifer from literatures (e.g. Xu et al., 2004; Marini, 2006) were adopted. CGS simulations were assumed with a constant CO2 injection rate of 1 Mt/yr at the first 50 years. Hydrogeological settings included porosities of 0.103 for shale, 0.141 for interbedding sandstone and shale, and 0.179 for sandstone; initial pore pressure distributions of 24.5 MPa to 28.7 MPa, an ambient temperature of 70°C, and 0.5 M of NaCl in aqueous solution. Mineral compositions were modified from Xu et al. (2006) to include calcite (1.9 vol. % of solid), quartz (57.9 %), kaolinite (2.0 %), illite (1.0 %), oligoclase (19.8 %), Na-smectite (3.9 %), K-feldspar (8.2 %), chlorite (4.6 %), and hematite (0.5 %) and were

Geomechanical Response of Jointed Caprock During CO2 Geological Sequestration

Science.gov (United States)

Newell, P.; Martinez, M. J.; Bishop, J. E.

2014-12-01

Geological sequestration of CO2 refers to the injection of supercritical CO2 into deep reservoirs trapped beneath a low-permeability caprock formation. Maintaining caprock integrity during the injection process is the most important factor for a successful injection. In this work we evaluate the potential for jointed caprock during injection scenarios using coupled three-dimensional multiphase flow and geomechanics modeling. Evaluation of jointed/fractured caprock systems is of particular concern to CO2 sequestration because creation or reactivation of joints (mechanical damage) can lead to enhanced pathways for leakage. In this work, we use an equivalent continuum approach to account for the joints within the caprock. Joint's aperture and non-linear stiffness of the caprock will be updated dynamically based on the effective normal stress. Effective permeability field will be updated based on the joints' aperture creating an anisotropic permeability field throughout the caprock. This feature would add another coupling between the solid and fluid in addition to basic Terzaghi's effective stress concept. In this study, we evaluate the impact of the joint's orientation and geometry of caprock and reservoir layers on geomechanical response of the CO2 geological systems. This work is supported as part of the Center for Frontiers of Subsurface Energy Security, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DE-SC0001114. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-AC04-94AL85000.

Recovery Act: Develop a Modular Curriculum for Training University Students in Industry Standard CO{sub 2} Sequestration and Enhanced Oil Recovery Methodologies

Energy Technology Data Exchange (ETDEWEB)

Trentham, R. C.; Stoudt, E. L.

2013-05-31

CO{sub 2} Enhanced Oil Recovery, Sequestration, & Monitoring Measuring & Verification are topics that are not typically covered in Geoscience, Land Management, and Petroleum Engineering curriculum. Students are not typically exposed to the level of training that would prepare them for CO{sub 2} reservoir and aquifer sequestration related projects when they begin assignments in industry. As a result, industry training, schools & conferences are essential training venues for new & experienced personnel working on CO{sub 2} projects for the first time. This project collected and/or generated industry level CO{sub 2} training to create modules which faculties can utilize as presentations, projects, field trips and site visits for undergrad and grad students and prepare them to "hit the ground running" & be contributing participants in CO{sub 2} projects with minimal additional training. In order to create the modules, UTPB/CEED utilized a variety of sources. Data & presentations from industry CO{sub 2} Flooding Schools & Conferences, Carbon Management Workshops, UTPB Classes, and other venues was tailored to provide introductory reservoir & aquifer training, state-of-the-art methodologies, field seminars and road logs, site visits, and case studies for students. After discussions with faculty at UTPB, Sul Ross, Midland College, other universities, and petroleum industry professionals, it was decided to base the module sets on a series of road logs from Midland to, and through, a number of Permian Basin CO{sub 2} Enhanced Oil Recovery (EOR) projects, CO{sub 2} Carbon Capture and Storage (CCUS) projects and outcrop equivalents of the formations where CO{sub 2} is being utilized or will be utilized, in EOR projects in the Permian Basin. Although road logs to and through these projects exist, none of them included CO{sub 2} specific information. Over 1400 miles of road logs were created, or revised specifically to highlight CO{sub 2} EOR projects. After testing a number of

Pre injection characterisation and evaluation of CO{sub 2} sequestration potential in the Haizume formation, Niigata basin, Japan; Caracterisation avant injection et evaluation du potentiel de sequestration de CO{sub 2} dans la formation de Haizume, bassin de Niigata, Japon. Modelisation geochimique des interactions eau-mineraux-CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Zwingmann, N. [CSIRO Petroleum, ARRC, Bentley, WA (Australia); Mito, S.; Sorai, M.; Ohsumi, T. [RITE, Kyoto (Japan); Zwingmann, N. [Western, Univ. (Australia); Sorai, M. [Mitsubishi Research Institute, Inc. (Japan)

2005-03-15

The Research Institute of Innovative Technology for the Earth (RITE) is carrying out a small-scale CO{sub 2} injection field experiment to investigate the feasibility of geological sequestration of CO{sub 2} greenhouse gas in the south-west of Nagaoka City, Niigata Prefecture, Japan. Prior to the injection geochemical reactions caused by CO{sub 2} injections were investigated using the geochemical modelling code (EQ3/6). The injection formation is the sedimentary marine Haizume Formation (Pleistocene) in the Uonuma Group, which is covered by a mud-stone seal. The formation is mainly composed of quartz, plagioclase, feldspar, pyroxene, and clays (smectite, chlorite). The sandstone shows minor consolidation and grain size is medium to coarse sand. The total dissolved solid (TDS) of the formation water is approximately 6100 mg/l and the water contains a high Ca{sup 2+} ({>=} 20% of Na{sup +} concentration). The geochemical model was used for an initial adjustment of the formation water chemistry to the formation conditions and a modelling of the formation water-mineral-CO{sub 2} reactions. The modelling results showed a high reactivity of the minerals in the CO{sub 2} rich environment and high mineral conversion rate within the formation. At the final state, approximately 23 mol of CO{sub 2} were taken into 1 kg of formation water and more than 90% of this was stored within carbonate minerals. In this simulation, some uncertainty is associated with the time scale and a more detailed investigation is planned and will address accurate evaluation. (authors)

The Carbonation of Wollastonite: A Model Reaction to Test Natural and Biomimetic Catalysts for Enhanced CO2 Sequestration

Directory of Open Access Journals (Sweden)

Fulvio Di Lorenzo

2018-05-01

Full Text Available One of the most promising strategies for the safe and permanent disposal of anthropogenic CO2 is its conversion into carbonate minerals via the carbonation of calcium and magnesium silicates. However, the mechanism of such a reaction is not well constrained, and its slow kinetics is a handicap for the implementation of silicate mineral carbonation as an effective method for CO2 capture and storage (CCS. Here, we studied the different steps of wollastonite (CaSiO3 carbonation (silicate dissolution → carbonate precipitation as a model CCS system for the screening of natural and biomimetic catalysts for this reaction. Tested catalysts included carbonic anhydrase (CA, a natural enzyme that catalyzes the reversible hydration of CO2(aq, and biomimetic metal-organic frameworks (MOFs. Our results show that dissolution is the rate-limiting step for wollastonite carbonation. The overall reaction progresses anisotropically along different [hkl] directions via a pseudomorphic interface-coupled dissolution–precipitation mechanism, leading to partial passivation via secondary surface precipitation of amorphous silica and calcite, which in both cases is anisotropic (i.e., (hkl-specific. CA accelerates the final carbonate precipitation step but hinders the overall carbonation of wollastonite. Remarkably, one of the tested Zr-based MOFs accelerates the dissolution of the silicate. The use of MOFs for enhanced silicate dissolution alone or in combination with other natural or biomimetic catalysts for accelerated carbonation could represent a potentially effective strategy for enhanced mineral CCS.

Effect of Mineral Dissolution/Precipitation and CO2 Exsolution on CO2 transport in Geological Carbon Storage.

Science.gov (United States)

Xu, Ruina; Li, Rong; Ma, Jin; He, Di; Jiang, Peixue

2017-09-19

Geological carbon sequestration (GCS) in deep saline aquifers is an effective means for storing carbon dioxide to address global climate change. As the time after injection increases, the safety of storage increases as the CO 2 transforms from a separate phase to CO 2 (aq) and HCO 3 - by dissolution and then to carbonates by mineral dissolution. However, subsequent depressurization could lead to dissolved CO 2 (aq) escaping from the formation water and creating a new separate phase which may reduce the GCS system safety. The mineral dissolution and the CO 2 exsolution and mineral precipitation during depressurization change the morphology, porosity, and permeability of the porous rock medium, which then affects the two-phase flow of the CO 2 and formation water. A better understanding of these effects on the CO 2 -water two-phase flow will improve predictions of the long-term CO 2 storage reliability, especially the impact of depressurization on the long-term stability. In this Account, we summarize our recent work on the effect of CO 2 exsolution and mineral dissolution/precipitation on CO 2 transport in GCS reservoirs. We place emphasis on understanding the behavior and transformation of the carbon components in the reservoir, including CO 2 (sc/g), CO 2 (aq), HCO 3 - , and carbonate minerals (calcite and dolomite), highlight their transport and mobility by coupled geochemical and two-phase flow processes, and consider the implications of these transport mechanisms on estimates of the long-term safety of GCS. We describe experimental and numerical pore- and core-scale methods used in our lab in conjunction with industrial and international partners to investigate these effects. Experimental results show how mineral dissolution affects permeability, capillary pressure, and relative permeability, which are important phenomena affecting the input parameters for reservoir flow modeling. The porosity and the absolute permeability increase when CO 2 dissolved water is

Geothermal energy combined with CO2 sequestration : An additional benefit

NARCIS (Netherlands)

Salimi, H.; Wolf, K.H.A.A.; Bruining, J.

2012-01-01

In this transition period from a fossil-fuel based society to a sustainable-energy society, it is expected that CO2 capture and subsequent sequestration in geological formations plays a major role in reducing greenhouse gas emissions. An alternative for CO2 emission reduction is to partially replace

Gas-water-rock interactions induced by reservoir exploitation, CO2 sequestration, and other geological storage

International Nuclear Information System (INIS)

Lecourtier, J.

2005-01-01

Here is given a summary of the opening address of the IFP International Workshop: 'gas-water-rock interactions induced by reservoir exploitation, CO 2 sequestration, and other geological storage' (18-20 November 2003). 'This broad topic is of major interest to the exploitation of geological sites since gas-water-mineral interactions determine the physicochemical characteristics of these sites, the strategies to adopt to protect the environment, and finally, the operational costs. Modelling the phenomena is a prerequisite for the engineering of a geological storage, either for disposal efficiency or for risk assessment and environmental protection. During the various sessions, several papers focus on the great achievements that have been made in the last ten years in understanding and modelling the coupled reaction and transport processes occurring in geological systems, from borehole to reservoir scale. Remaining challenges such as the coupling of mechanical processes of deformation with chemical reactions, or the influence of microbiological environments on mineral reactions will also be discussed. A large part of the conference programme will address the problem of mitigating CO 2 emissions, one of the most important issues that our society must solve in the coming years. From both a technical and an economic point of view, CO 2 geological sequestration is the most realistic solution proposed by the experts today. The results of ongoing pilot operations conducted in Europe and in the United States are strongly encouraging, but geological storage will be developed on a large scale in the future only if it becomes possible to predict the long term behaviour of stored CO 2 underground. In order to reach this objective, numerous issues must be solved: - thermodynamics of CO 2 in brines; - mechanisms of CO 2 trapping inside the host rock; - geochemical modelling of CO 2 behaviour in various types of geological formations; - compatibility of CO 2 with oil-well cements

Carbon dioxide sequestration by aqueous mineral carbonation of magnesium silicate minerals

Energy Technology Data Exchange (ETDEWEB)

Gerdemann, Stephen J.; Dahlin, David C.; O' Connor, William K.; Penner, Larry R.

2003-01-01

The dramatic increase in atmospheric carbon dioxide since the Industrial Revolution has caused concerns about global warming. Fossil-fuel-fired power plants contribute approximately one third of the total human-caused emissions of carbon dioxide. Increased efficiency of these power plants will have a large impact on carbon dioxide emissions, but additional measures will be needed to slow or stop the projected increase in the concentration of atmospheric carbon dioxide. By accelerating the naturally occurring carbonation of magnesium silicate minerals it is possible to sequester carbon dioxide in the geologically stable mineral magnesite (MgCO3). The carbonation of two classes of magnesium silicate minerals, olivine (Mg2SiO4) and serpentine (Mg3Si2O5(OH)4), was investigated in an aqueous process. The slow natural geologic process that converts both of these minerals to magnesite can be accelerated by increasing the surface area, increasing the activity of carbon dioxide in the solution, introducing imperfections into the crystal lattice by high-energy attrition grinding, and in the case of serpentine, by thermally activating the mineral by removing the chemically bound water. The effect of temperature is complex because it affects both the solubility of carbon dioxide and the rate of mineral dissolution in opposing fashions. Thus an optimum temperature for carbonation of olivine is approximately 185 degrees C and 155 degrees C for serpentine. This paper will elucidate the interaction of these variables and use kinetic studies to propose a process for the sequestration of the carbon dioxide.

The impact of CO2 on shallow groundwater chemistry: observations at a natural analog site and implications for carbon sequestration

Energy Technology Data Exchange (ETDEWEB)

Keating, Elizabeth [Los Alamos National Laboratory; Fessenden, Julianna [Los Alamos National Laboratory; Kanjorski, Nancy [NON LANL; Koning, Dan [NM BUREAU OF GEOLOGY AND MINERAL RESOURCES; Pawar, Rajesh [Los Alamos National Laboratory

2008-01-01

In a natural analog study of risks associated with carbon sequestration, impacts of CO{sub 2} on shallow groundwater quality have been measured in a sandstone aquifer in New Mexico, USA. Despite relatively high levels of dissolved CO{sub 2}, originating from depth and producing geysering at one well, pH depression and consequent trace element mobility are relatively minor effects due to the buffering capacity of the aquifer. However, local contamination due to influx of saline waters in a subset of wells is significant. Geochemical modeling of major ion concentrations suggests that high alkalinity and carbonate mineral dissolution buffers pH changes due to CO{sub 2} influx. Analysis oftrends in dissolved trace elements, chloride, and CO2 reveal no evidence of in-situ trace element mobilization. There is clear evidence, however, that As, U, and Pb are locally co-transported into the aquifer with CO{sub 2}-rich saline water. This study illustrates the role that local geochemical conditions will play in determining the effectiveness of monitoring strategies for CO{sub 2} leakage. For example, if buffering is significant, pH monitoring may not effectively detect CO2 leakage. This study also highlights potential complications that CO{sub 2}carrier fluids, such as saline waters, pose in monitoring impacts ofgeologic sequestration.

Natural CO2 Analogs for Carbon Sequestration

Energy Technology Data Exchange (ETDEWEB)

Scott H. Stevens; B. Scott Tye

2005-07-31

The report summarizes research conducted at three naturally occurring geologic CO{sub 2} fields in the US. The fields are natural analogs useful for the design of engineered long-term storage of anthropogenic CO{sub 2} in geologic formations. Geologic, engineering, and operational databases were developed for McElmo Dome in Colorado; St. Johns Dome in Arizona and New Mexico; and Jackson Dome in Mississippi. The three study sites stored a total of 2.4 billion t (46 Tcf) of CO{sub 2} equivalent to 1.5 years of power plant emissions in the US and comparable in size with the largest proposed sequestration projects. The three CO{sub 2} fields offer a scientifically useful range of contrasting geologic settings (carbonate vs. sandstone reservoir; supercritical vs. free gas state; normally pressured vs. overpressured), as well as different stages of commercial development (mostly undeveloped to mature). The current study relied mainly on existing data provided by the CO{sub 2} field operator partners, augmented with new geochemical data. Additional study at these unique natural CO{sub 2} accumulations could further help guide the development of safe and cost-effective design and operation methods for engineered CO{sub 2} storage sites.

Adsorption of Dissolved Gases (CH4, CO2, H2, Noble Gases) by Water-Saturated Smectite Clay Minerals

Science.gov (United States)

Bourg, I. C.; Gadikota, G.; Dazas, B.

2016-12-01

Adsorption of dissolved gases by water-saturated clay minerals plays important roles in a range of fields. For example, gas adsorption in on clay minerals may significantly impact the formation of CH4 hydrates in fine-grained sediments, the behavior of CH4 in shale, CO2 leakage across caprocks of geologic CO2 sequestration sites, H2 leakage across engineered clay barriers of high-level radioactive waste repositories, and noble gas geochemistry reconstructions of hydrocarbon migration in the subsurface. Despite its importance, the adsorption of gases on clay minerals remains poorly understood. For example, some studies have suggested that clay surfaces promote the formation of CH4 hydrates, whereas others indicate that clay surfaces inhibit the formation of CH4 hydrates. Here, we present molecular dynamics (MD) simulations of the adsorption of a range of gases (CH4, CO2, H2, noble gases) on clay mineral surfaces. Our results indicate that the affinity of dissolved gases for clay mineral surfaces has a non-monotone dependence on the hydrated radius of the gas molecules. This non-monotone dependence arises from a combination of two effects: the polar nature of certain gas molecules (in particular, CO2) and the templating of interfacial water structure by the clay basal surface, which results in the presence of interfacial water "cages" of optimal size for intermediate-size gas molecules (such as Ne or Ar).

Enclathration of CO2 as a co-guest of structure H hydrates and its implications for CO2 capture and sequestration

International Nuclear Information System (INIS)

Lee, Yohan; Lee, Dongyoung; Lee, Jong-Won; Seo, Yongwon

2016-01-01

Highlights: • We examine sH hydrates with CO 2 + N 2 + neohexane for CO 2 capture and sequestration. • The structural transition occurs in the CO 2 (40%) + N 2 (60%) + neohexane system. • CO 2 molecules are enclathrated into sH hydrates in the N 2 -rich systems. • CO 2 selectivity in sH hydrates is slightly lower than that in sI hydrates. • ΔH d values provide information on the structural transition of sH to sI hydrates. - Abstract: In this study, the thermodynamic behaviors, cage-specific guest distributions, structural transition, and dissociation enthalpies of sH hydrates with CO 2 + N 2 gas mixtures were investigated for their potential applications to hydrate-based CO 2 capture and sequestration. The stability conditions of the CO 2 + N 2 + water systems and the CO 2 + N 2 + neohexane (2,2-dimethylbutane, NH) + water systems indicated that the gas mixtures in the range of flue gas compositions could form sH hydrates, thereby mitigating the pressure and temperature required for gas hydrate formation. Structure identification using powder X-ray diffraction (PXRD) revealed the coexistence of sI and sH hydrates in the CO 2 (40%) + N 2 (60%) + NH system and the hydrate structure transformed from sH into sI as the CO 2 concentration increased. In addition, the Raman analysis clearly demonstrated that CO 2 molecules were enclathrated into the cages of sH hydrates in the N 2 -rich systems. It was found from direct CO 2 composition measurements that CO 2 selectivity in the sH hydrate phase was slightly lower than that in the corresponding sI hydrate phase. Dissociation enthalpy (ΔH d ) measurements using a high-pressure micro-differential scanning calorimeter (HP μ-DSC) indicated that the ΔH d values could also provide valuable information on the structural transition of sH to sI hydrates with respect to the CO 2 concentration in the feed gas. This study provides a better understanding of the thermodynamic and physicochemical background for CO 2

A review of accelerated carbonation technology in the treatment of cement-based materials and sequestration of CO2

International Nuclear Information System (INIS)

Fernandez Bertos, M.; Simons, S.J.R.; Hills, C.D.; Carey, P.J.

2004-01-01

Moist calcium silicate minerals are known to readily react with carbon dioxide (CO 2 ). The reaction products can cause rapid hardening and result in the production of monolithic materials. Today, accelerated carbonation is a developing technology, which may have potential for the treatment of wastes and contaminated soils and for the sequestration of CO 2 , an important greenhouse gas. This paper reviews recent developments in this emerging technology and provides information on the parameters that control the process. The effects of the accelerated carbonation reaction on the solid phase are discussed and future potential applications of this technology are also considered

Prediction of CO2 leakage during sequestration into marine sedimentary strata

International Nuclear Information System (INIS)

Li, Qi; Wu Zhishen; Li Xiaochun

2009-01-01

Deep ocean storage of CO 2 could help reduce the atmospheric level of greenhouse gas as part of a climate change mitigation strategy. In this paper, a multiphase flow model of CO 2 sequestration into deep ocean sediments was designed associated with the formation of CO 2 hydrates. A simplified assumption was proposed to predict the critical time of CO 2 leakage from marine sedimentary strata into seawater. Moreover, some principal parameters, which include the permeability, anisotropy, total injection amount, and length of the injection part of wellbores, were investigated by numerical simulations. The numerical estimates are used to assess the feasibility and effectiveness of CO 2 storage in deep ocean sediments. Accurately predicting the actual fate of liquid CO 2 sequestered into the marine sedimentary strata at depths greater than 500 m is complicated by uncertainties associated with not only the chemical-physical behavior of CO 2 under such conditions but also the geo-environment of disposal sites. Modeling results have shown some implications that the effectiveness of CO 2 ocean sequestration depends mainly on the injection conditions (such as injection rate, total injection amount, and the depth of injection), the site geology (such as permeability and anisotropy of disposal formations), and the chemical-physical behavior of CO 2 in marine environment

Experimental observation and numerical simulation of permeability changes in dolomite at CO2 sequestration conditions

Science.gov (United States)

Tutolo, B. M.; Luhmann, A. J.; Kong, X.; Saar, M. O.; Seyfried, W. E.

2013-12-01

Injecting surface temperature CO2 into geothermally warm reservoirs for geologic storage or energy production may result in depressed temperature near the injection well and thermal gradients and mass transfer along flow paths leading away from the well. Thermal gradients are particularly important to consider in reservoirs containing carbonate minerals, which are more soluble at lower temperatures, as well as in CO2-based geothermal energy reservoirs where lowering heat exchanger rejection temperatures increases efficiency. Additionally, equilibrating a fluid with cation-donating silicates near a low-temperature injection well and transporting the fluid to higher temperature may enhance the kinetics of mineral precipitation in such a way as to overcome the activation energy required for mineral trapping of CO2. We have investigated this process by subjecting a dolomite core to a 650-hour temperature series experiment in which the fluid was saturated with CO2 at high pressure (110-126 bars) and 21°C. This fluid was recirculated through the dolomite core, increasing permeability from 10-16 to 10-15.2 m2. Subsequently, the core temperature was raised to 50° C, and permeability decreased to 10-16.2 m2 after 289 hours, due to thermally-driven CO2 exsolution. Increasing core temperature to 100°C for the final 145 hours of the experiment caused dolomite to precipitate, which, together with further CO2 exsolution, decreased permeability to 10-16.4 m2. Post-experiment x-ray computed tomography and scanning electron microscope imagery of the dolomite core reveals abundant matrix dissolution and enlargement of flow paths at low temperatures, and subsequent filling-in of the passages at elevated temperature by dolomite. To place this experiment within the broader context of geologic CO2 sequestration, we designed and utilized a reactive transport simulator that enables dynamic calculation of CO2 equilibrium constants and fugacity and activity coefficients by incorporating

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

Interdisciplinary Investigation of CO2 Sequestration in Depleted Shale Gas Formations

Energy Technology Data Exchange (ETDEWEB)

Zoback, Mark D. [Stanford Univ., CA (United States); Kovscek, Anthony R. [Stanford Univ., CA (United States); Wilcox, Jennifer [Stanford Univ., CA (United States)

2013-09-30

This project investigates the feasibility of geologic sequestration of CO2 in depleted shale gas reservoirs from an interdisciplinary viewpoint. It is anticipated that over the next two decades, tens of thousands of wells will be drilled in the 23 states in which organic-rich shale gas deposits are found. This research investigates the feasibility of using these formations for sequestration. If feasible, the number of sites where CO2 can be sequestered increases dramatically. The research embraces a broad array of length scales ranging from the ~10 nanometer scale of the pores in the shale formations to reservoir scale through a series of integrated laboratory and theoretical studies.

Numerical Simulations for Enhanced Methane Recovery from Gas Hydrate Accumulations by Utilizing CO2 Sequestration

Science.gov (United States)

Sridhara, Prathyusha

transport properties with change in pressure and temperature due to the presence of the simple CO2-hydrate and mixed hydrates (mainly CH4-CO2 hydrate and CH4 -CO2-N2 hydrate) in the porous geologic media. These simulations on CO2/ CH4-CO2 hydrate reservoirs provided a basic insight to formulate and interpret a novel technological approach. This approach aims at prediction of enhanced gas production profiles from Class 2 hydrate accumulations by utilizing CO2 sequestration. The approach also offers a possibility to permanently store CO 2 in the geologic formation to a greater extent compared to a direct injection of CO2 into gas hydrate sediments. The production technique implies a three-stage approach using one vertical well design. In Stage I, the CO2 is injected into the underlying aquifer. In Stage II, the well is shut in and injected CO2 is allowed to be converted into immobile CO2 hydrate. Finally, during Stage III, decomposition of CH4 hydrate is induced by the depressurization method. The gas production potential is estimated over 15 years. The results reveal that methane production is increased together with simultaneous reduction of concomitant water production rate comparing to a conventional Class 2 reservoir production.

Multiphase Flow in Porous Media with Emphasis on Co2 Sequestration

International Nuclear Information System (INIS)

Be, Alif

2011-01-01

Numerical simulation has been used to predict multiphase flow in porous media. It is of great importance to incorporate accurate flow properties to obtain a proper simulation result thus reducing the risk of making wrong decision. Relative permeability and capillary pressure are important key parameters in multiphase flow as they describe how different fluid will interact in porous media. It is even more important in the case of three-phase flow as there are more fluid phases interact in the system. In most of the three-phase flow studies, capillary pressure has been neglected due to the lack of measured data and assumption that its effect is negligible. In other cases, two-phase capillary pressure has been used instead to describe the process in the system. This study will try to show how significant the impact of three-phase capillary pressure using different rock wettability. The three-phase capillary pressure surfaces are generated using a network model. Prior research shows that rock wettability is altered during Co2 sequestration due to the formation of carbonic acid (H2CO3) which leads to lower ph. In this study the effect of wettability alteration is incorporated to assess the safety of Johansen formation which is a good candidate for Co2 sequestration project. In addition, the wettability alteration effect to different flow parameters such as heterogeneity, solubility and diffusion is investigated. This thesis consists of two parts; the first part presents a theoretical background for the work, and the second part is a collection of papers. The papers are grouped into two main topics. The first three papers are discussing about three-phase flow simulation in porous media. The rest are discussing about wettability alteration during Co2 sequestration. Chapter 2 and 3 of the theoretical background include definitions and descriptions of interfacial tension, wettability, capillary pressure, relative permeability and hysteresis. Network model and technique for

Precipitation of hydrated Mg carbonate with the aid of carbonic anhydrase for CO2 sequestration

Science.gov (United States)

Power, I. M.; Harrison, A. L.; Dipple, G. M.

2011-12-01

and water was sampled for dissolved inorganic carbon (DIC) and magnesium concentrations. Final precipitates were collected for X-ray powder diffraction and determination of the percent carbon. The presence of BCA increases the concentration of DIC, thus accelerating the rate-limiting step. In alkaline Mg-rich solutions, disordered hydrated magnesium carbonate, resembling dypingite, rapidly precipitated within hours to form micron-wide flakes. At concentrations of 200 and 100 mg BCA/L, the rates of carbon uptake were ~7 and ~4.4 times that of the control system during the first 24 hours, respectively. BCA is able to catalyze the hydration of CO2 thereby increasing concentrations of DIC relatively rapidly and allowing for the sequestration of atmospheric CO2 as hydrated Mg carbonate minerals.

Faults as Windows to Monitor Gas Seepage: Application to CO2 Sequestration and CO2-EOR

Directory of Open Access Journals (Sweden)

Ronald W. Klusman

2018-03-01

Full Text Available Monitoring of potential gas seepage for CO2 sequestration and CO2-EOR (Enhanced Oil Recovery in geologic storage will involve geophysical and geochemical measurements of parameters at depth and at, or near the surface. The appropriate methods for MVA (Monitoring, Verification, Accounting are needed for both cost and technical effectiveness. This work provides an overview of some of the geochemical methods that have been demonstrated to be effective for an existing CO2-EOR (Rangely, CA, USA and a proposed project at Teapot Dome, WY, USA. Carbon dioxide and CH4 fluxes and shallow soil gas concentrations were measured, followed by nested completions of 10-m deep holes to obtain concentration gradients. The focus at Teapot Dome was the evaluation of faults as pathways for gas seepage in an under-pressured reservoir system. The measurements were supplemented by stable carbon and oxygen isotopic measurements, carbon-14, and limited use of inert gases. The work clearly demonstrates the superiority of CH4 over measurements of CO2 in early detection and quantification of gas seepage. Stable carbon isotopes, carbon-14, and inert gas measurements add to the verification of the deep source. A preliminary accounting at Rangely confirms the importance of CH4 measurements in the MVA application.

ECONOMIC EVALUATION OF CO2 STORAGE AND SINK ENHANCEMENT OPTIONS

Energy Technology Data Exchange (ETDEWEB)

Bert Bock; Richard Rhudy; Howard Herzog; Michael Klett; John Davison; Danial G. De La Torre Ugarte; Dale Simbeck

2003-02-01

This project developed life-cycle costs for the major technologies and practices under development for CO{sub 2} storage and sink enhancement. The technologies evaluated included options for storing captured CO{sub 2} in active oil reservoirs, depleted oil and gas reservoirs, deep aquifers, coal beds, and oceans, as well as the enhancement of carbon sequestration in forests and croplands. The capture costs for a nominal 500 MW{sub e} integrated gasification combined cycle plant from an earlier study were combined with the storage costs from this study to allow comparison among capture and storage approaches as well as sink enhancements.

A disconnect between O horizon and mineral soil carbon - Implications for soil C sequestration

Science.gov (United States)

Garten, Charles T., Jr.

2009-03-01

Changing inputs of carbon to soil is one means of potentially increasing carbon sequestration in soils for the purpose of mitigating projected increases in atmospheric CO 2 concentrations. The effect of manipulations of aboveground carbon input on soil carbon storage was tested in a temperate, deciduous forest in east Tennessee, USA. A 4.5-year experiment included exclusion of aboveground litterfall and supplemental litter additions (three times ambient) in an upland and a valley that differed in soil nitrogen availability. The estimated decomposition rate of the carbon stock in the O horizon was greater in the valley than in the upland due to higher litter quality (i.e., lower C/N ratios). Short-term litter exclusion or addition had no effect on carbon stock in the mineral soil, measured to a depth of 30 cm, or the partitioning of carbon in the mineral soil between particulate- and mineral-associated organic matter. A two-compartment model was used to interpret results from the field experiments. Field data and a sensitivity analysis of the model were consistent with little carbon transfer between the O horizon and the mineral soil. Increasing aboveground carbon input does not appear to be an effective means of promoting carbon sequestration in forest soil at the location of the present study because a disconnect exists in carbon dynamics between O horizon and mineral soil. Factors that directly increase inputs to belowground soil carbon, via roots, or reduce decomposition rates of organic matter are more likely to benefit efforts to increase carbon sequestration in forests where carbon dynamics in the O horizon are uncoupled from the mineral soil.

Pore-scale studies of multiphase flow and reaction involving CO2 sequestration in geologic formations

Science.gov (United States)

Kang, Q.; Wang, M.; Lichtner, P. C.

2008-12-01

In geologic CO2 sequestration, pore-scale interfacial phenomena ultimately govern the key processes of fluid mobility, chemical transport, adsorption, and reaction. However, spatial heterogeneity at the pore scale cannot be resolved at the continuum scale, where averaging occurs over length scales much larger than typical pore sizes. Natural porous media, such as sedimentary rocks and other geological media encountered in subsurface formations, are inherently heterogeneous. This pore-scale heterogeneity can produce variabilities in flow, transport, and reaction processes that take place within a porous medium, and can result in spatial variations in fluid velocity, aqueous concentrations, and reaction rates. Consequently, the unresolved spatial heterogeneity at the pore scale may be important for reactive transport modeling at the larger scale. In addition, current continuum models of surface complexation reactions ignore a fundamental property of physical systems, namely conservation of charge. Therefore, to better understand multiphase flow and reaction involving CO2 sequestration in geologic formations, it is necessary to quantitatively investigate the influence of the pore-scale heterogeneity on the emergent behavior at the field scale. We have applied the lattice Boltzmann method to simulating the injection of CO2 saturated brine or supercritical CO2 into geological formations at the pore scale. Multiple pore-scale processes, including advection, diffusion, homogeneous reactions among multiple aqueous species, heterogeneous reactions between the aqueous solution and minerals, ion exchange and surface complexation, as well as changes in solid and pore geometry are all taken into account. The rich pore scale information will provide a basis for upscaling to the continuum scale.

CO{sub 2} sequestration; Sequestration du CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Acket, C

2008-04-15

The carbon dioxide is the main gas associated to the human activity, generating consequences on the greenhouse effect. By the use of fossil fuels, the human activity generates each year, about 26 milliards of tons. Only the half of theses releases is absorbed by the nature, the rest reinforces the greenhouse effect. To reduce the emissions two actions are proposed: a better energy consumption and the development of technologies which do not produce, or weakly, greenhouse effect gases. Another way is studied: the carbon sequestration and geological storage. This document details the different technologies of sequestration, the transport and the underground storage. It discusses also the economical and legislative aspects, providing examples and projects. (A.L.B.)

Geomechanical issues of anthropogenic CO2 sequestration in exploited gas fields

International Nuclear Information System (INIS)

Ferronato, Massimiliano; Gambolati, Giuseppe; Janna, Carlo; Teatini, Pietro

2010-01-01

Anthropogenic CO 2 sequestration in deep geological formations may represent a viable option to fulfil the requirements of the 1997 Kyoto protocol on the reduction of greenhouse gas emissions. Scenarios of CO 2 sequestration through three injection wells in an exploited gas field located in the Po sedimentary basin (Italy) are simulated with the final target to understand the geomechanical consequences of the injection of carbon dioxide. Investigated scenarios include, as a hypothetical case, the long-term injection of CO 2 until the initial reservoir pressure is exceeded by as much as 40% over a period of about 100 years. The process is analyzed from the geomechanical point of view using a finite element-interface element (FE-IE) model with the following main issues addressed: (1) prediction of the possible land vertical uplift and corresponding impact on the ground infrastructures; (2) evaluation of the stress state induced in the reservoir formation with the possible generation of fractures and (3) a risk analysis for the activation of existing faults. The geomechanical constitutive law of the Northern Adriatic basin relying on the radioactive marker interpretation is implemented into the FE model, while an elasto-plastic relationship based on the Mohr-Coulomb criterion is used for the IE reproducing the fault behaviour. The in situ stress prior to the gas field exploitation is compressive with the principal horizontal stress in the direction perpendicular to the major faults equal to the vertical stress. The results show that the ground surface rebound due to the overpressure generated by the CO 2 sequestration partially mitigates the land subsidence experienced by the area because of the previous gas field depletion with differential displacements that are confined within the safety bounds suggested in the literature for the surface infrastructures. Activation of a few faults lying close to the northern reservoir boundary points to a slip of a couple of

Carbon sequestration.

Science.gov (United States)

Lal, Rattan

2008-02-27

Developing technologies to reduce the rate of increase of atmospheric concentration of carbon dioxide (CO2) from annual emissions of 8.6PgCyr-1 from energy, process industry, land-use conversion and soil cultivation is an important issue of the twenty-first century. Of the three options of reducing the global energy use, developing low or no-carbon fuel and sequestering emissions, this manuscript describes processes for carbon (CO2) sequestration and discusses abiotic and biotic technologies. Carbon sequestration implies transfer of atmospheric CO2 into other long-lived global pools including oceanic, pedologic, biotic and geological strata to reduce the net rate of increase in atmospheric CO2. Engineering techniques of CO2 injection in deep ocean, geological strata, old coal mines and oil wells, and saline aquifers along with mineral carbonation of CO2 constitute abiotic techniques. These techniques have a large potential of thousands of Pg, are expensive, have leakage risks and may be available for routine use by 2025 and beyond. In comparison, biotic techniques are natural and cost-effective processes, have numerous ancillary benefits, are immediately applicable but have finite sink capacity. Biotic and abiotic C sequestration options have specific nitches, are complementary, and have potential to mitigate the climate change risks.

CO2 Energy Reactor - Integrated Mineral Carbonation: Perspectives on Lab-Scale Investigation and Products Valorization

OpenAIRE

Rafael M Santos; Pol CM Knops; Keesjan L Rijnsburger; Yi Wai eChiang

2016-01-01

To overcome the challenges of mineral CO2 sequestration, Innovation Concepts B.V. is developing a unique proprietary gravity pressure vessel (GPV) reactor technology and has focussed on generating reaction products of high economic value. The GPV provides intense process conditions through hydrostatic pressurization and heat exchange integration that harvests exothermic reaction energy, thereby reducing energy demand of conventional reactor designs, in addition to offering other benefits. In ...

Direct gas-solid carbonation kinetics of steel slag and the contribution to in situ sequestration of flue gas CO(2) in steel-making plants.

Science.gov (United States)

Tian, Sicong; Jiang, Jianguo; Chen, Xuejing; Yan, Feng; Li, Kaimin

2013-12-01

Direct gas-solid carbonation of steel slag under various operational conditions was investigated to determine the sequestration of the flue gas CO2 . X-ray diffraction analysis of steel slag revealed the existence of portlandite, which provided a maximum theoretical CO2 sequestration potential of 159.4 kg CO 2 tslag (-1) as calculated by the reference intensity ratio method. The carbonation reaction occurred through a fast kinetically controlled stage with an activation energy of 21.29 kJ mol(-1) , followed by 10(3) orders of magnitude slower diffusion-controlled stage with an activation energy of 49.54 kJ mol(-1) , which could be represented by a first-order reaction kinetic equation and the Ginstling equation, respectively. Temperature, CO2 concentration, and the presence of SO2 impacted on the carbonation conversion of steel slag through their direct and definite influence on the rate constants. Temperature was the most important factor influencing the direct gas-solid carbonation of steel slag in terms of both the carbonation conversion and reaction rate. CO2 concentration had a definite influence on the carbonation rate during the kinetically controlled stage, and the presence of SO2 at typical flue gas concentrations enhanced the direct gas-solid carbonation of steel slag. Carbonation conversions between 49.5 % and 55.5 % were achieved in a typical flue gas at 600 °C, with the maximum CO2 sequestration amount generating 88.5 kg CO 2 tslag (-1) . Direct gas-solid carbonation of steel slag showed a rapid CO2 sequestration rate, high CO2 sequestration amounts, low raw-material costs, and a large potential for waste heat utilization, which is promising for in situ carbon capture and sequestration in the steel industry. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Feasibility of CO2 Sequestration as a Closure Option for Underground Coal Mine

Science.gov (United States)

Ray, Sutapa; Dey, Kaushik

2018-01-01

The Kyoto Protocol, 1998, was signed by member countries to reduce greenhouse gas (GHG) emissions to a minimum acceptable level. India agreed to Kyoto Protocol since 2002 and started its research on GHG mitigation. Few researchers have carried out research work on CO2 sequestration in different rock formations. However, CO2 sequestration in abandoned mines has yet not drawn its attention largely. In the past few years or decades, a significant amount of research and development has been done on Carbon Capture and Storage (CCS) technologies, since it is a possible solution for assuring less emission of CO2 to the atmosphere from power plants and some other major industrial plants. CCS mainly involves three steps: (a) capture and compression of CO2 from source (power plants and industrial areas), (b) transportation of captured CO2 to the storage mine and (c) injecting CO2 into underground mine. CO2 is stored at an underground mine mainly in three forms: (1) adsorbed in the coals left as pillars of the mine, (2) absorbed in water through a chemical process and (3) filled in void with compressed CO2. Adsorption isotherm is a graph developed between the amounts of adsorbate adsorbed on the surface of adsorbent and the pressure at constant temperature. Various types of adsorption isotherms are available, namely, Freundlich, Langmuir and BET theory. Indian coal is different in origin from most of the international coal deposits and thus demands isotherm experiments of the same to arrive at the right adsorption isotherm. To carry out these experiments, adsorption isotherm set up is fabricated in the laboratory with a capacity to measure the adsorbed volume up to a pressure level of 100 bar. The coal samples are collected from the pillars and walls of the underground coal seam using a portable drill machine. The adsorption isotherm experiments have been carried out for the samples taken from a mine. From the adsorption isotherm experiments, Langmuir Equation is found to be

Feasibility of CO2 Sequestration as a Closure Option for Underground Coal Mine

Science.gov (United States)

Ray, Sutapa; Dey, Kaushik

2018-04-01

The Kyoto Protocol, 1998, was signed by member countries to reduce greenhouse gas (GHG) emissions to a minimum acceptable level. India agreed to Kyoto Protocol since 2002 and started its research on GHG mitigation. Few researchers have carried out research work on CO2 sequestration in different rock formations. However, CO2 sequestration in abandoned mines has yet not drawn its attention largely. In the past few years or decades, a significant amount of research and development has been done on Carbon Capture and Storage (CCS) technologies, since it is a possible solution for assuring less emission of CO2 to the atmosphere from power plants and some other major industrial plants. CCS mainly involves three steps: (a) capture and compression of CO2 from source (power plants and industrial areas), (b) transportation of captured CO2 to the storage mine and (c) injecting CO2 into underground mine. CO2 is stored at an underground mine mainly in three forms: (1) adsorbed in the coals left as pillars of the mine, (2) absorbed in water through a chemical process and (3) filled in void with compressed CO2. Adsorption isotherm is a graph developed between the amounts of adsorbate adsorbed on the surface of adsorbent and the pressure at constant temperature. Various types of adsorption isotherms are available, namely, Freundlich, Langmuir and BET theory. Indian coal is different in origin from most of the international coal deposits and thus demands isotherm experiments of the same to arrive at the right adsorption isotherm. To carry out these experiments, adsorption isotherm set up is fabricated in the laboratory with a capacity to measure the adsorbed volume up to a pressure level of 100 bar. The coal samples are collected from the pillars and walls of the underground coal seam using a portable drill machine. The adsorption isotherm experiments have been carried out for the samples taken from a mine. From the adsorption isotherm experiments, Langmuir Equation is found to be

Exploration of the Role of Heat Activation in Enhancing Serpentine Carbon Sequestration Reactions

International Nuclear Information System (INIS)

McKelvy, M.J.; Chizmeshya, A.V.G.; Diefenbacher, J.; Bearat, H.; Wolf, G.

2005-01-01

As compared with other candidate carbon sequestration technologies, mineral carbonation offers the unique advantage of permanent disposal via geologically stable and environmentally benign carbonates. The primary challenge is the development of an economically viable process. Enhancing feedstock carbonation reactivity is key. Heat activation dramatically enhances aqueous serpentine carbonation reactivity. Although the present process is too expensive to implement, the materials characteristics and mechanisms that enhance carbonation are of keen interest for further reducing cost. Simultaneous thermogravimetric and differential thermal analysis (TGA/DTA) of the serpentine mineral lizardite was used to isolate a series of heat-activated materials as a function of residual hydroxide content at progressively higher temperatures. Their structure and composition are evaluated via TGA/DTA, X-ray powder diffraction (including phase analysis), and infrared analysis. The meta-serpentine materials that were observed to form ranged from those with longer range ordering, consistent with diffuse stage-2 like interlamellar order, to an amorphous component that preferentially forms at higher temperatures. The aqueous carbonation reaction process was investigated for representative materials via in situ synchrotron X-ray diffraction. Magnesite was observed to form directly at 15 MPa CO 2 and at temperatures ranging from 100 to 125 C. Carbonation reactivity is generally correlated with the extent of meta-serpentine formation and structural disorder.

Still needed data for successful deep CO2 sequestration

International Nuclear Information System (INIS)

Ulmer, Gene C.

2013-01-01

Despite chemical knowledge about CO 2 that extends back centuries, some data bases are still evolving that are needed to predict even the sub-critical CO 2 behavior down the geothermal gradient's P- and T-values which will be encountered in sequestration utilizing deep mines and wells. These needed data include IR-spectral interpretations of CO 2 molecular structure as P and T change; the unraveling of the Joule Thomson coefficient (heating or cooling?) that changes algebraic polarity around 10 6 Pa; more exact equations of state (EOS) that correlate to potential CO 2 polarity changes in molecular structure; newer EOS than those that have currently been derived by templating directly measured data; and focus is needed on the EOS-derived properties, like fugacity. Also, natural analogues like (1) the carbonate stability in metamorphic silicate-carbonation facies and (2) Lake Nyos aqueous geochemistry with concern about the potential redox-equilibria-predicted presence of CO (and graphite), as well as CO 2 . (authors)

Modeling CO2-Water-Mineral Wettability and Mineralization for Carbon Geosequestration.

Science.gov (United States)

Liang, Yunfeng; Tsuji, Shinya; Jia, Jihui; Tsuji, Takeshi; Matsuoka, Toshifumi

2017-07-18

Carbon dioxide (CO 2 ) capture and storage (CCS) is an important climate change mitigation option along with improved energy efficiency, renewable energy, and nuclear energy. CO 2 geosequestration, that is, to store CO 2 under the subsurface of Earth, is feasible because the world's sedimentary basins have high capacity and are often located in the same region of the world as emission sources. How CO 2 interacts with the connate water and minerals is the focus of this Account. There are four trapping mechanisms that keep CO 2 in the pores of subsurface rocks: (1) structural trapping, (2) residual trapping, (3) dissolution trapping, and (4) mineral trapping. The first two are dominated by capillary action, where wettability controls CO 2 and water two-phase flow in porous media. We review state-of-the-art studies on CO 2 /water/mineral wettability, which was found to depend on pressure and temperature conditions, salt concentration in aqueous solutions, mineral surface chemistry, and geometry. We then review some recent advances in mineral trapping. First, we show that it is possible to reproduce the CO 2 /water/mineral wettability at a wide range of pressures using molecular dynamics (MD) simulations. As the pressure increases, CO 2 gas transforms into a supercritical fluid or liquid at ∼7.4 MPa depending on the environmental temperature. This transition leads to a substantial decrease of the interfacial tension between CO 2 and reservoir brine (or pure water). However, the wettability of CO 2 /water/rock systems depends on the type of rock surface. Recently, we investigated the contact angle of CO 2 /water/silica systems with two different silica surfaces using MD simulations. We found that contact angle increased with pressure for the hydrophobic (siloxane) surface while it was almost constant for the hydrophilic (silanol) surface, in excellent agreement with experimental observations. Furthermore, we found that the CO 2 thin films at the CO 2 -hydrophilic

Density-Driven Flow Simulation in Anisotropic Porous Media: Application to CO2 Geological Sequestration

KAUST Repository

Negara, Ardiansyah; Salama, Amgad; Sun, Shuyu

2014-01-01

Carbon dioxide (CO2) sequestration in saline aquifers is considered as one of the most viable and promising ways to reduce CO2 concentration in the atmosphere. CO2 is injected into deep saline formations at supercritical state where its density

Total soil C and N sequestration in a grassland following 10 years of free air CO2 enrichment

NARCIS (Netherlands)

Kessel, van C.; Boots, B.; Graaff, de M.A.; Harris, D.; Blum, H.; Six, J.

2006-01-01

Soil C sequestration may mitigate rising levels of atmospheric CO2. However, it has yet to be determined whether net soil C sequestration occurs in N-rich grasslands exposed to long-term elevated CO2. This study examined whether N-fertilized grasslands exposed to elevated CO2 sequestered additional

Time-Lapse Seismic Monitoring and Performance Assessment of CO₂ Sequestration in Hydrocarbon Reservoirs

Energy Technology Data Exchange (ETDEWEB)

Datta-Gupta, Akhil [Texas Engineering Experiment Station, College Station, TX (United States)

2017-06-15

Carbon dioxide sequestration remains an important and challenging research topic as a potentially viable approach for mitigating the effects of greenhouse gases on global warming (e.g., Chu and Majumdar, 2012; Bryant, 2007; Orr, 2004; Hepple and Benson, 2005; Bachu, 2003; Grimston et al., 2001). While CO₂ can be sequestered in oceanic or terrestrial biomass, the most mature and effective technology currently available is sequestration in geologic formations, especially in known hydrocarbon reservoirs (Barrufet et al., 2010; Hepple and Benson, 2005). However, challenges in the design and implementation of sequestration projects remain, especially over long time scales. One problem is that the tendency for gravity override caused by the low density and viscosity of CO₂. In the presence of subsurface heterogeneity, fractures and faults, there is a significant risk of CO₂ leakage from the sequestration site into overlying rock compared to other liquid wastes (Hesse and Woods, 2010; Ennis-King and Patterson, 2002; Tsang et al., 2002). Furthermore, the CO₂ will likely interact chemically with the rock in which it is stored, so that understanding and predicting its transport behavior during sequestration can be complex and difficult (Mandalaparty et al., 2011; Pruess et al., 2003). Leakage of CO₂ can lead to such problems as acidification of ground water and killing of plant life, in addition to contamination of the atmosphere (Ha-Duong, 2003; Gasda et al., 2004). The development of adequate policies and regulatory systems to govern sequestration therefore requires improved characterization of the media in which CO₂ is stored and the development of advanced methods for detecting and monitoring its flow and transport in the subsurface (Bachu, 2003).

Effects of freshwater Synechococcus sp. cyanobacteria pH buffering on CaCO3 precipitation: Implications for CO2 sequestration

International Nuclear Information System (INIS)

Martinez, Raul E.; Weber, Sebastian; Grimm, Christian

2016-01-01

In the present study, a mixed-flow steady-state bio-reactor was designed to biomineralize CO 2 as a consequence of photosynthesis from active Synechococcus sp. Dissolved CO 2 , generated by constant air bubbling of inorganic and cyanobacteria stock solutions, was the only source of inorganic carbon. The release of hydroxide ion by cyanobacteria from photosynthesis maintained highly alkaline pH conditions. In the presence of Ca 2+ and carbonate species, this led to calcite supersaturation under steady state conditions. Ca 2+ remained constant throughout the experiments showing the presence of steady state conditions. Similarly, the Synechococcus sp. biomass concentration remained stable within uncertainty. A gradual pH decrease was observed for the highest Ca 2+ condition coinciding with the formation of CaCO 3 . The high degree of supersaturation, under steady-state conditions, contributed to the stabilization of calcite and maintained a constant driving force for the mineral nucleation and growth. For the highest Ca 2+ condition a fast crystal growth rate was consistent with rapid calcite precipitation as suggested further by affinity calculations. Although saturation state based kinetic precipitation models cannot accurately reflect the controls on crystal growth kinetics or reliably predict growth mechanisms, the relatively reaction orders obtained from modeling of calcite precipitation rates as function of decreasing carbonate concentration suggest that the precipitation occurred via surface-controlled rate determining reactions. These high reaction orders support in addition the hypothesis that crystal growth proceeded through complex surface controlled mechanisms. In conclusion, the steady state supersaturated conditions generated by a constant cyanobacteria biomass and metabolic activity strongly suggest that these microorganisms could be used for the development of efficient CO 2 sequestration methods in a controlled large-scale environment. - Highlights: �

Determining CO2 storage potential during miscible CO2 enhanced oil recovery: Noble gas and stable isotope tracers

Science.gov (United States)

Shelton, Jenna L.; McIntosh, Jennifer C.; Hunt, Andrew; Beebe, Thomas L; Parker, Andrew D; Warwick, Peter D.; Drake, Ronald; McCray, John E.

2016-01-01

Rising atmospheric carbon dioxide (CO2) concentrations are fueling anthropogenic climate change. Geologic sequestration of anthropogenic CO2 in depleted oil reservoirs is one option for reducing CO2 emissions to the atmosphere while enhancing oil recovery. In order to evaluate the feasibility of using enhanced oil recovery (EOR) sites in the United States for permanent CO2 storage, an active multi-stage miscible CO2flooding project in the Permian Basin (North Ward Estes Field, near Wickett, Texas) was investigated. In addition, two major natural CO2 reservoirs in the southeastern Paradox Basin (McElmo Dome and Doe Canyon) were also investigated as they provide CO2 for EOR operations in the Permian Basin. Produced gas and water were collected from three different CO2 flooding phases (with different start dates) within the North Ward Estes Field to evaluate possible CO2 storage mechanisms and amounts of total CO2retention. McElmo Dome and Doe Canyon were sampled for produced gas to determine the noble gas and stable isotope signature of the original injected EOR gas and to confirm the source of this naturally-occurring CO2. As expected, the natural CO2produced from McElmo Dome and Doe Canyon is a mix of mantle and crustal sources. When comparing CO2 injection and production rates for the CO2 floods in the North Ward Estes Field, it appears that CO2 retention in the reservoir decreased over the course of the three injections, retaining 39%, 49% and 61% of the injected CO2 for the 2008, 2010, and 2013 projects, respectively, characteristic of maturing CO2 miscible flood projects. Noble gas isotopic composition of the injected and produced gas for the flood projects suggest no active fractionation, while δ13CCO2 values suggest no active CO2dissolution into formation water, or mineralization. CO2 volumes capable of dissolving in residual formation fluids were also estimated along with the potential to store pure-phase supercritical CO2. Using a combination

GEOLOGIC SCREENING CRITERIA FOR SEQUESTRATION OF CO2 IN COAL: QUANTIFYING POTENTIAL OF THE BLACK WARRIOR COALBED METHANE FAIRWAY, ALABAMA

Energy Technology Data Exchange (ETDEWEB)

Jack C. Pashin; Richard E. Carroll; Richard H. Groshong, Jr.; Dorothy E. Raymond; Marcella McIntyre; J. Wayne Payton

2003-01-01

Sequestration of CO{sub 2} in coal has potential to reduce greenhouse gas emissions from coal-fired power plants while enhancing coalbed methane recovery. Data from more than 4,000 coalbed methane wells in the Black Warrior basin of Alabama provide an opportunity to quantify the carbon sequestration potential of coal and to develop a geologic screening model for the application of carbon sequestration technology. This report summarizes stratigraphy and sedimentation, structural geology, geothermics, hydrology, coal quality, gas capacity, and production characteristics of coal in the Black Warrior coalbed methane fairway and the implications of geology for carbon sequestration and enhanced coalbed methane recovery. Coal in the Black Warrior basin is distributed among several fluvial-deltaic coal zones in the Lower Pennsylvanian Pottsville Formation. Most coal zones contain one to three coal beds that are significant targets for coalbed methane production and carbon sequestration, and net coal thickness generally increases southeastward. Pottsville strata have effectively no matrix permeability to water, so virtually all flow is through natural fractures. Faults and folds influence the abundance and openness of fractures and, hence, the performance of coalbed methane wells. Water chemistry in the Pottsville Formation ranges from fresh to saline, and zones with TDS content lower than 10,000 mg/L can be classified as USDW. An aquifer exemption facilitating enhanced recovery in USDW can be obtained where TDS content is higher than 3,000 mg/L. Carbon dioxide becomes a supercritical fluid above a temperature of 88 F and a pressure of 1,074 psi. Reservoir temperature exceeds 88 F in much of the study area. Hydrostatic pressure gradients range from normal to extremely underpressured. A large area of underpressure is developed around closely spaced longwall coal mines, and areas of natural underpressure are distributed among the coalbed methane fields. The mobility and

Screening and ranking Alberta oil pools for CO{sub 2} flooding and sequestration

Energy Technology Data Exchange (ETDEWEB)

Shaw, J.C. [Adams Pearson Associates Inc., Calgary, AB (Canada); Bachu, S. [Alberta Energy and Utilities Board, Calgary, AB (Canada)

2001-06-01

This paper presented the results of a technical screening program using Excel VBA to successfully screen and rank a very large number of oil pools for enhanced oil recovery using carbon dioxide (CO{sub 2}) flooding. A total of 6 ranking parameters were used, including API gravity of oil, residual oil saturation, ratio between reservoir pressure and minimum miscibility pressure, reservoir temperature, net pay thickness and porosity. The screening program provided a technical ranking of approximately 8,800 Alberta pools in less than 2 minutes. After compilation of the Alberta oil pools, it was determined that most of the deep carbonate oil pools are excellent candidates for CO{sub 2} miscible flooding. Other Devonian carbonate pools were also ranked as having high potential for the process. An environmental benefit of CO{sub 2} miscible flooding process is that carbon sequestration has the potential to reduce anthropogenic carbon dioxide emissions from reaching the atmosphere. Ongoing studies are currently addressing CO{sub 2} capture and transportation, making EOR technology viable for maintaining light oil production in western Canada. 11 refs., 7 tabs., 1 fig.

Fundamentals of carbon dioxide-enhanced oil recovery (CO2-EOR): a supporting document of the assessment methodology for hydrocarbon recovery using CO2-EOR associated with carbon sequestration

Science.gov (United States)

Verma, Mahendra K.

2015-01-01

The objective of this report is to provide basic technical information regarding the CO2-EOR process, which is at the core of the assessment methodology, to estimate the technically recoverable oil within the fields of the identified sedimentary basins of the United States. Emphasis is on CO2-EOR because this is currently one technology being considered as an ultimate long-term geologic storage solution for CO2 owing to its economic profitability from incremental oil production offsetting the cost of carbon sequestration.

CO2 sequestration: Storage capacity guideline needed

Science.gov (United States)

Frailey, S.M.; Finley, R.J.; Hickman, T.S.

2006-01-01

Petroleum reserves are classified for the assessment of available supplies by governmental agencies, management of business processes for achieving exploration and production efficiency, and documentation of the value of reserves and resources in financial statements. Up to the present however, the storage capacity determinations made by some organizations in the initial CO2 resource assessment are incorrect technically. New publications should thus cover differences in mineral adsorption of CO2 and dissolution of CO2 in various brine waters.

CO2 emissions: mineral carbonation and Finnish pulp and paper industry (CO2 Nordic Plus) and use of serpentinites in energy and metal industry (ECOSERP)

International Nuclear Information System (INIS)

Fogelholm, C.-J.; Raiski, T.; Teir, S.

2007-01-01

Abstract Mineral carbonation has been investigated at Helsinki University of Technology (TKK), laboratory of energy engineering and environmental protection since year 2000. The Finnish Technology Agency Tekes and the Finnish Recovery Boiler Committee are funding through the ClimBus technology programme, in conjunction with the Nordic Energy Research Programme, the research regarding the application of ex situ mineral carbonation processes. One aspect is to verify the possible use of mineral carbonation for the separation, utilisation and long-term storage of carbon dioxide (CO 2 ) in the pulp and paper industry. The Geological Survey of Finland (GTK) has been screening since 2004 the location, quality and suitability of the Finnish processed serpentine and stoped serpentinite storage of mines and in situ serpentinite bodies of ultramafic rock formations for mineral carbonation of CO 2 . Tekes and the GTK are funding development work through the ClimBus technology programme on the utilisation of serpentine and serpentinite for CO 2 sequestration purposes, based on economical and environmental evaluation of mineral and mining processing operations. Also the options for other use of serpentine and serpentinite are evaluated. The most promising magnesium- and calcium-based sources for carbonation are by-products of mining processes of ultramafic rocks (such as serpentinites and serpentine) and steelmaking slags. Carbonated minerals could possibly be used as paper coating materials (PCC), fillers or construction materials. For magnesium carbonate new markets and applications must be developed. (orig.)

Uncertainties in relation to CO2 capture and sequestration. Preliminary results. Working Paper

International Nuclear Information System (INIS)

Gielen, D.

2003-03-01

This paper has been presented at an expert meeting on CO2 capture technology learning at the IEA headquarters, January 24th, 2003. The electricity sector is a key source of CO2 emissions and a strong increase of emissions is forecast in a business-as-usual scenario. A range of strategies have been proposed to reduce these emissions. This paper focuses on one of the promising strategies, CO2 capture and storage. The future role of CO2 capture in the electricity sector has been assessed, using the Energy Technology Perspectives model (ETP). Technology data have been collected and reviewed in cooperation with the IEA Greenhouse Gas R and D implementing agreement and other expert groups. CO2 capture and sequestration is based on relatively new technology. Therefore, its characteristics and its future role in the energy system is subject to uncertainties, as for any new technology. The analysis suggests that the choice of a reference electricity production technology and the characteristics of the CO2 storage option constitute the two main uncertainties, apart from a large number of other factors of lesser importance. Based on the choices made cost estimates can range from less than zero USD for coal fired power plants to more than 150 USD per ton of CO2 for gas fired power plants. The results suggest that learning effects are important, but they do not affect the CO2 capture costs significantly, other uncertainties dominate the cost estimates. The ETP model analysis, where choices are based on the ideal market hypothesis and rational price based decision making, suggest up to 18% of total global electricity production will be equipped with CO2 capture by 2040, in case of a penalty of 50 US$ per ton of CO2. However this high penetration is only achieved in case coal fired IGCC-SOFC power plants are developed successfully. Without such technology only a limited amount of CO2 is captured from gas fired power plants. Higher penalties may result in a higher share of CO2

Potential for CO2 sequestration and enhanced coalbed methane production in the Netherlands

NARCIS (Netherlands)

Hamelinck, C.N.; Schreurs, H.; Faaij, A.P.C.; Ruijg, G.J.; Jansen, Daan; Pagnier, H.; Bergen, F. van; Wolf, K.-H.; Barzandji, O.; Bruining, H.

2006-01-01

This study investigated the technical and economic feasibility of using CO2 for the enhanced production of coal bed methane (ECBM) in the Netherlands. This concept could lead to both CO2 storage by adsorbing CO2 in deep coal layers that are not suitable for mining, as well as production of methane.

Modeling carbon sequestration in afforestation, agroforestry and forest management projects: the CO2FIX V.2 approach

NARCIS (Netherlands)

Masera, O.R.; Garza-Caligaris, J.F.; Kanninen, M.; Karjalainen, T.; Liski, J.; Nabuurs, G.J.; Pussinen, A.; Jong de, B.H.J.; Mohren, G.M.J.

2003-01-01

The paper describes the Version 2 of the CO2FIX (CO2FIX V.2) model, a user-friendly tool for dynamically estimating the carbon sequestration potential of forest management, agroforesty and afforestation projects. CO2FIX V.2 is a multi-cohort ecosystem-level model based on carbon accounting of forest

Magnesium hydroxide extracted from a magnesium-rich mineral for CO2 sequestration in a gas-solid system.

Science.gov (United States)

Lin, Pao-Chung; Huang, Cheng-Wei; Hsiao, Ching-Ta; Teng, Hsisheng

2008-04-15

Magnesium hydroxide extracted from magnesium-bearing minerals is considered a promising agent for binding CO2 as a carbonate mineral in a gas-solid reaction. An efficient extraction route consisting of hydrothermal treatment on serpentine in HCl followed by NaOH titration for Mg(OH)2 precipitation was demonstrated. The extracted Mg(OH)2 powder had a mean crystal domain size as small as 12 nm and an apparent surface area of 54 m2/g. Under one atmosphere of 10 vol% CO2/N2, carbonation of the serpentine-derived Mg(OH)2 to 26% of the stoichiometric limit was achieved at 325 degrees C in 2 h; while carbonation of a commercially available Mg(OH)2, with a mean crystal domain size of 33 nm and an apparent surface area of 3.5 m2/g, reached only 9% of the stoichiometric limit. The amount of CO2 fixation was found to be inversely proportional to the crystal domain size of the Mg(OH)2 specimens. The experimental data strongly suggested that only a monolayer of carbonates was formed on the crystal domain boundary in the gas-solid reaction, with little penetration of the carbonates into the crystal domain.

Acute physiological impacts of CO2 ocean sequestration on marine animals

International Nuclear Information System (INIS)

Ishimatsu, A.; Hayashi, M.; Lee, K.S.; Murata, K.; Kumagai, E.

2005-01-01

The biological impacts of ocean carbon dioxide (CO 2 ) sequestration must be carefully considered before it is implemented as a mitigation strategy. This paper presented details of a study investigating the effects of high CO 2 concentrations on marine fish, lobster, and octopus. The influence of water temperature on the physiological effects of CO 2 was also discussed. In the first part of the study, eggs and larvae of red seabream were exposed to both CO 2 and HCI-acidified seawater at identical pH levels. Seabream in the CO 2 group showed a much higher mortality rate than fish in the HCI group. Other tests showed that Japanese Flounder died after complete recovery of pH in seawater equilibrated with 5 per cent CO 2 . Cardiac output was rapidly depressed in Yellowtail fish without significant changes in blood oxygen concentrations. Lower temperatures resulted in higher mortality and delayed pH recovery during hypercapnia in all fish. Western rock lobsters were the most tolerant to CO 2 among all species tested. The recovery of hemolymph pH was complete at exposure to CO 2 concentrations of 1 per cent. Changes in hemolymph bicarbonate concentrations indicated that acid-based regulatory mechanisms differed between fish and lobsters. Mortality rates for octopus were significant at CO 2 concentrations of 1 per cent. The results of all tests showed that aquatic animals are more susceptible to increases in ambient CO 2 levels than terrestrial animals. It was concluded that even slight elevations in CO 2 concentration levels adversely affected physiological functioning in the tested species. It was concluded that CO 2 sequestration in deeper, colder waters will have a more pronounced effect on aquatic animals due to the interactions between CO 2 and lower temperatures, as well as the fact that most deep-sea fish are less tolerant to environmental perturbations. 3 refs., 1 tab., 3 figs

Potential for CO2 sequestration and enhanced coalbed methane production in the Netherlands

OpenAIRE

Hamelinck, C.N.; Schreurs, H.; Faaij, A.P.C.; Ruijg, G.J.; Jansen, Daan; Pagnier, H.; Bergen, F. van; Wolf, K.-H.; Barzandji, O.; Bruining, H.

2006-01-01

This study investigated the technical and economic feasibility of using CO2 for the enhanced production of coal bed methane (ECBM) in the Netherlands. This concept could lead to both CO2 storage by adsorbing CO2 in deep coal layers that are not suitable for mining, as well as production of methane. For every two molecules of CO2 injected, roughly one molecule of methane is produced. The work included an investigation of the potential CBM reserves in the Dutch underground and the related CO2 s...

Estimation of the reactive mineral surface area during CO2-rich fluid-rock interaction: the influence of neogenic phases

Science.gov (United States)

Scislewski, A.; Zuddas, P.

2010-12-01

with CO2-rich fluids, decreasing the effective reactive surface area. Predictive models of CO2 sequestration under geological conditions should take into account the inhibiting role of surface coating formation. The CO2 rich fluid-rock interactions may also have significant consequences on metal mobilization. Our results indicated that the formation of stable carbonate complexes enhances the solubility of uranium minerals of both albitite and granite, facilitating the U(IV) oxidation, and limiting the extent of uranium adsorption onto particles in oxidized waters. This clearly produces an increase of the uranium mobility with significant consequences for the environment.

Numerical assessments of geological CO2 sequestration in the Changhua Coastal Industrial Park, Central Taiwan

Science.gov (United States)

Sung, R.; Li, M.

2012-12-01

Coal-fired power plants of the Taiwan Power Company are the main sources of CO2 emission in Taiwan. Due to the importation of coal mine and the need of cooling water circulation, power plants were built on the coast. Geological CO2 sequestration has been recognized as one of solutions for reducing anthropogenic CO2 emission by injecting CO2 captured from fossil fuel power plants into deep saline geologic formations. The Changhua Coastal Industrial Park (CCIP; 120.38° E, 24.11° N) in central Taiwan has been preliminary evaluated as one of potential sites for geological CO2 sequestration. The CCIP site has a sloping, layered heterogeneity formation with stagnant groundwater flow. Layers of sandstone and shale sequentially appeared to be the major components of geological formations with seaward transgression. Thickness of sedimentary formations gradually becomes thinner from east to west. Previous investigations [Chiao et al., 2010; Yu et al, 2011] did not find significant faults around this site. The TOUGHREACT/ECO2N model was employed with external mesh generator developed in this study to proceed to comprehensive assessments for CO2 injection into deep saline aquifers (salinity of 3%, pH of 7.2) at the CCIP site. A series of numerical experiments for investigating the physical, geochemical and its interactions included the deep saline-aquifer responses, CO2 plume migration, leakage risks, hydrogeochemistry processes, reservoir capacity and trapping mechanisms (i.e. hydrodynamics, capillarity, solubility, and mineral trapping) during and post CO2 injection were assessed. A 3-D lithological model applied in this study was conceptualized with two seismic profiles (along shore and cross shore) and one geological well nearby the study area. A total of 32 vertical layers was built with different porosities and permeabilities estimated from the TCDP-A borehole log samples adjusted with effects in geopressure differences. Cross-platform open source libraries of the CGAL

LIBS Sensor for Sub-surface CO2 Leak Detection in Carbon Sequestration

Directory of Open Access Journals (Sweden)

Jinesh JAIN

2017-07-01

Full Text Available Monitoring carbon sequestration poses numerous challenges to the sensor community. For example, the subsurface environment is notoriously harsh, with large potential mechanical, thermal, and chemical stresses, making long-term stability and survival a challenge to any potential in situ monitoring method. Laser induced breakdown spectroscopy (LIBS has been demonstrated as a promising technology for chemical monitoring of harsh environments and hard to reach places. LIBS has a real- time monitoring capability and can be used for the elemental and isotopic analysis of solid, liquid, and gas samples. The flexibility of the probe design and the use of fiber- optics has made LIBS particularly suited for remote measurements. The paper focuses on developing a LIBS instrument for downhole high-pressure, high-temperature brine experiments, where CO2 leakage could result in changes in the trace mineral composition of an aquifer. The progress in fabricating a compact, robust, and simple LIBS sensor for widespread subsurface leak detection is presented.

Consequences of co-benefits for the efficient design of carbon sequestration programs

International Nuclear Information System (INIS)

Feng, H.; Kling, C.L.

2005-01-01

The social efficiency of private carbon markets that also included trading in agricultural soil carbon sequestration with significant associated co-benefits were considered. Three topics related to the presence of co-benefits that sequester carbon were examined: (1) the consequences of co-benefits from carbon sinks and carbon abatement technology on the efficiency of carbon markets; (2) the efficient supply of carbon sequestration and co-benefits when there is spatial heterogeneity; and (3) the consequences of the presence of a carbon market when there is also a government supported conservation program. Co-benefits from carbon sinks and abatement were considered in relation to the socially efficient level of sequestration. The supply of carbon sequestration and co-benefits were then considered when fields differed in their potential to provide carbon and other environmental benefits. An empirical example of the economic characteristics of carbon sequestration and co-benefits in the Upper Mississippi River Basin was presented, in which the sequestration practice of land retirement with planting of perennial grasses was examined. Two sets of figures were used to illustrate the relationship between the cost of carbon sequestration and its marginal co-benefits: the marginal cost and the marginal co-benefits of carbon sequestration in a carbon market; and the marginal cost of carbon sequestration under a policy designed to maximize a bundle of environmental benefits. It was demonstrated that the relationship between carbon and its associated co-benefits will affect the efficiency of policy instruments designed for carbon sequestration. It was recommended that policy-makers consider that there are already a multitude of existing conservation programmes that result in significant carbon sequestration in many countries, and that nascent carbon markets are emerging in countries that have not ratified the Kyoto Protocol. The efficient level and location of carbon

Testing CO2 Sequestration in an Alkaline Soil Treated with Flue Gas Desulfurization Gypsum (FGDG)

Science.gov (United States)

Han, Y.; Tokunaga, T. K.

2012-12-01

Identifying effective and economical methods for increasing carbon storage in soils is of interest for reducing soil CO2 fluxes to the atmosphere in order to partially offset anthropogenic CO2 contributions to climate change This study investigates an alternative strategy for increasing carbon retention in soils by accelerating calcite (CaCO3) precipitation and promoting soil organic carbon (SOC) complexation on mineral surfaces. The addition of calcium ion to soils with pH > 8, often found in arid and semi-arid regions, may accelerate the slow process of calcite precipitation. Increased ionic strength from addition of a soluble Ca source also suppresses microbial activity which oxidizes SOC to gaseous CO2. Through obtaining C mass balances in soil profiles, this study is quantifying the efficiency of gypsum amendments for mitigating C losses to the atmosphere. The objective of this study is to identify conditions in which inorganic and organic C sequestration is practical in semi-arid and arid soils by gypsum treatment. As an inexpensive calcium source, we proposed to use flue gas desulfurization gypsum (FGDG), a byproduct of fossil fuel burning electric power plants. To test the hypothesis, laboratory column experiments have been conducted in calcite-buffered soil with addition of gypsum and FGDG. The results of several months of column monitoring are demonstrating that gypsum-treated soil have lowered amounts of soil organic carbon loss and increased inorganic carbon (calcite) production. The excess generation of FGDG relative to industrial and agricultural needs, FGDG, is currently regarded as waste. Thus application of FGDG application in some soils may be an effective and economical means for fixing CO2 in soil organic and inorganic carbon forms.Soil carbon cycle, with proposed increased C retention by calcite precipitation and by SOC binding onto soil mineral surfaces, with both processes driven by calcium released from gypsum dissolution.

Summary Report on CO{sub 2} Geologic Sequestration & Water Resources Workshop

Energy Technology Data Exchange (ETDEWEB)

Varadharajan, C.; Birkholzer, J.; Kraemer, S.; Porse, S.; Carroll, S.; Wilkin, R.; Maxwell, R.; Bachu, S.; Havorka, S.; Daley, T.; Digiulio, D.; Carey, W.; Strasizar, B.; Huerta, N.; Gasda, S.; Crow, W.

2012-02-15

The United States Environmental Protection Agency (EPA) and Lawrence Berkeley National Laboratory (LBNL) jointly hosted a workshop on “CO{sub 2} Geologic Sequestration and Water Resources” in Berkeley, June 1–2, 2011. The focus of the workshop was to evaluate R&D needs related to geological storage of CO{sub 2} and potential impacts on water resources. The objectives were to assess the current status of R&D, to identify key knowledge gaps, and to define specific research areas with relevance to EPA’s mission. About 70 experts from EPA, the DOE National Laboratories, industry, and academia came to Berkeley for two days of intensive discussions. Participants were split into four breakout session groups organized around the following themes: Water Quality and Impact Assessment/Risk Prediction; Modeling and Mapping of Area of Potential Impact; Monitoring and Mitigation; Wells as Leakage Pathways. In each breakout group, participants identified and addressed several key science issues. All groups developed lists of specific research needs; some groups prioritized them, others developed short-term vs. long-term recommendations for research directions. Several crosscutting issues came up. Most participants agreed that the risk of CO{sub 2} leakage from sequestration sites that are properly selected and monitored is expected to be low. However, it also became clear that more work needs to be done to be able to predict and detect potential environmental impacts of CO{sub 2} storage in cases where the storage formation may not provide for perfect containment and leakage of CO{sub 2}–brine might occur.

Sequestration and Enhanced Coal Bed Methane: Tanquary Farms Test Site, Wabash County, Illinois

Energy Technology Data Exchange (ETDEWEB)

Frailey, Scott; Parris, Thomas; Damico, James; Okwen, Roland; McKaskle, Ray; Monson, Charles; Goodwin, Jonathan; Beck, E; Berger, Peter; Butsch, Robert; Garner, Damon; Grube, John; Hackley, Keith; Hinton, Jessica; Iranmanesh, Abbas; Korose, Christopher; Mehnert, Edward; Monson, Charles; Roy, William; Sargent, Steven; Wimmer, Bracken

2012-05-01

The Midwest Geological Sequestration Consortium (MGSC) carried out a pilot project to test storage of carbon dioxide (CO{sub 2}) in the Springfield Coal Member of the Carbondale Formation (Pennsylvanian System), in order to gauge the potential for large-scale CO{sub 2} sequestration and/or enhanced coal bed methane recovery from Illinois Basin coal beds. The pilot was conducted at the Tanquary Farms site in Wabash County, southeastern Illinois. A four-well design an injection well and three monitoring wells was developed and implemented, based on numerical modeling and permeability estimates from literature and field data. Coal cores were taken during the drilling process and were characterized in detail in the lab. Adsorption isotherms indicated that at least three molecules of CO{sub 2} can be stored for each displaced methane (CH{sub 4}) molecule. Microporosity contributes significantly to total porosity. Coal characteristics that affect sequestration potential vary laterally between wells at the site and vertically within a given seam, highlighting the importance of thorough characterization of injection site coals to best predict CO{sub 2} storage capacity. Injection of CO{sub 2} gas took place from June 25, 2008, to January 13, 2009. A continuous injection period ran from July 21, 2008, to December 23, 2008, but injection was suspended several times during this period due to equipment failures and other interruptions. Injection equipment and procedures were adjusted in response to these problems. Approximately 92.3 tonnes (101.7 tons) of CO{sub 2} were injected over the duration of the project, at an average rate of 0.93 tonne (1.02 tons) per day, and a mode injection rate of 0.6-0.7 tonne/day (0.66-0.77 ton/day). A Monitoring, Verification, and Accounting (MVA) program was set up to detect CO{sub 2 leakage. Atmospheric CO{sub 2} levels were monitored as were indirect indicators of CO{sub 2} leakage such as plant stress, changes in gas composition at

W.A. Parish Post-Combustion CO{sub 2} Capture and Sequestration Project Phase 1 Definition

Energy Technology Data Exchange (ETDEWEB)

Armpriester, Anthony; Smith, Roger; Scheriffius, Jeff; Smyth, Rebecca; Istre, Michael

2014-02-01

For a secure and sustainable energy future, the United States (U.S.) must reduce its dependence on imported oil and reduce its emissions of carbon dioxide (CO{sub 2}) and other greenhouse gases (GHGs). To meet these strategic challenges, the U.S. wiU have to create fundamentally new technologies with performance levels far beyond what is now possible. Developing advanced post-combustion clean coal technologies for capturing CO{sub 2} from existing coal-fired power plants can play a major role in the country's transition to a sustainable energy future, especially when coupled with CO{sub 2}-enhanced oil recovery (CO{sub 2}-EOR). Pursuant to these goals, NRG Energy, Inc. (NRG) submitted an application and entered into a cost-shared collaboration with the U.S. Department of Energy (DOE) under Round 3 of the Clean Coal Power Initiative (CCPI) to advance low-emission coal technologies. The objective of the NRG W A Parish Post-Combustion CO{sub 2} Capture and Sequestration Demonstration Project is to establish the technical feasibility and economic viability of post-combustion CO{sub 2} capture using flue gas from an existing pulverized coal-fired boiler integrated with geologic sequestration via an enhanced oil recovery (EOR) process. To achieve these objectives, the project will be executed in three phases. Each phase represents a distinct aspect of the project execution. The project phases are: • Phase I. Project Definition/Front-End Engineering Design (FEED) • Phase ll. Detailed Engineering, Procurement & Construction • Phase III. Demonstration and Monitoring The purpose of Phase I is to develop the project in sufficient detail to facilitate the decision-making process in progressing to the next stage of project delivery. Phase n. This report provides a complete summary of the FEED study effort, including pertinent project background information, the scope of facilities covered, decisions, challenges, and considerations made regarding configuration and

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

Energy Technology Data Exchange (ETDEWEB)

Dr. T. Nakamura; Dr. Miguel Olaizola; Dr. Steven M. Masutani

2001-08-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO{sub 2} from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report covers the reporting period 1 April to 30 June 2001 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on the component optimization work. Aquasearch continued their effort on selection of microalgae suitable for CO{sub 2} sequestration. University of Hawaii initiated effort on system optimization of the CO{sub 2} sequestration system.

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

Energy Technology Data Exchange (ETDEWEB)

Dr. T. Nakamura; Dr. Miguel Olaizola; Dr. Stephen M. Masutani

2002-03-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO{sub 2} from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report covers the reporting period 1 October to 31 December 2001 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on the component optimization work. Aquasearch continued their effort on selection of microalgae suitable for CO{sub 2} sequestration. University of Hawaii initiated effort on system optimization of the CO{sub 2} sequestration system.

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

Energy Technology Data Exchange (ETDEWEB)

Dr. T. Nakamura; Dr. Miguel Olaizola; Dr. Stephen M. Masutani

2002-01-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO{sub 2} from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report is the summary first year report covering the reporting period 1 October 2000 to 30 September 2001 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on the component optimization work. Aquasearch continued their effort on selection of microalgae suitable for CO{sub 2} sequestration. University of Hawaii initiated effort on system optimization of the CO{sub 2} sequestration system.

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

International Nuclear Information System (INIS)

Dr. T. Nakamura; Dr. Miguel Olaizola; Dr. Stephen M. Masutani

2002-01-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO(sub 2) from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report covers the reporting period 1 October to 31 December 2001 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on the component optimization work. Aquasearch continued their effort on selection of microalgae suitable for CO(sub 2) sequestration. University of Hawaii initiated effort on system optimization of the CO(sub 2) sequestration system

Micromotor-Based Biomimetic Carbon Dioxide Sequestration: Towards Mobile Microscrubbers.

Science.gov (United States)

Uygun, Murat; Singh, Virendra V; Kaufmann, Kevin; Uygun, Deniz A; de Oliveira, Severina D S; Wang, Joseph

2015-10-26

We describe a mobile CO2 scrubbing platform that offers a greatly accelerated biomimetic sequestration based on a self-propelled carbonic anhydrase (CA) functionalized micromotor. The CO2 hydration capability of CA is coupled with the rapid movement of catalytic micromotors, and along with the corresponding fluid dynamics, results in a highly efficient mobile CO2 scrubbing microsystem. The continuous movement of CA and enhanced mass transport of the CO2 substrate lead to significant improvements in the sequestration efficiency and speed over stationary immobilized or free CA platforms. This system is a promising approach to rapid and enhanced CO2 sequestration platforms for addressing growing concerns over the buildup of greenhouse gas. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Potential for geological sequestration of CO{sub 2} in Switzerland - Final report; Studie zur Abschaetzung des Potenzials fuer CO{sub 2}-Sequestrierung in der Schweiz - Schlussbericht

Energy Technology Data Exchange (ETDEWEB)

Diamond, L. W.; Chevalier, G. [Institut fuer Geologie, Universitaet Bern, Bern (Switzerland); Leu, W. [Geoform AG, Geologische Beratungen und Studien, Villeneuve (former Minusio) (Switzerland)

2010-08-15

One approach to dispose of the greenhouse gas CO{sub 2} is to inject it into deep, porous geological formations, where is remains safely trapped over periods of many millennia. This report evaluates the potential for this option within Switzerland, based on a literature review. Only geological criteria for CO{sub 2} sequestration are taken into account, following international best-practice principles for reservoir safety. Simultaneous consideration of nine geological attributes (including faulting and natural seismicity) allows the sequestration potential to be mapped at a resolution of a few km{sup 2}, using a scale between 0 (negligible potential) and 1 (high potential). It is concluded that the crystalline rocks of the Alps and the sediments underlying the valleys of Valais, Ticino and Grisons are unsuitable for CO{sub 2} sequestration. However, the sedimentary rocks below the Central Plateau (and to lesser extent below the Jura Chain), locally show moderate to very good potential. At least four formations of porous sandstones and limestones (saline aquifers) underlie large areas of the Plateau within the technically favoured depth interval of 800-2500 m. Approximately 5000 km{sup 2} of the Plateau (mostly in the sector Fribourg-Olten-Lucerne) exhibits sequestration potentials above 0.6, offering a theoretical (unproven) storage capacity for approximately 2680 million tonnes of CO{sub 2}. From a purely geological point of view these results are promising. Although the high potentials do not guarantee the feasibility of CO{sub 2} sequestration, they serve as guides to areas that warrant detailed investigation. If this CO{sub 2} storage option is pursued in Switzerland, then more detailed geological investigations and a pilot study would be necessary to prove its feasibility. The assessed risks, leakage-monitoring procedures and non-geological criteria (proximity to CO{sub 2} point-sources, economics, conflicts of use of the subsurface, etc.) would have to be

Assessing ocean alkalinity for carbon sequestration

Science.gov (United States)

Renforth, Phil; Henderson, Gideon

2017-09-01

Over the coming century humanity may need to find reservoirs to store several trillions of tons of carbon dioxide (CO2) emitted from fossil fuel combustion, which would otherwise cause dangerous climate change if it were left in the atmosphere. Carbon storage in the ocean as bicarbonate ions (by increasing ocean alkalinity) has received very little attention. Yet recent work suggests sufficient capacity to sequester copious quantities of CO2. It may be possible to sequester hundreds of billions to trillions of tons of C without surpassing postindustrial average carbonate saturation states in the surface ocean. When globally distributed, the impact of elevated alkalinity is potentially small and may help ameliorate the effects of ocean acidification. However, the local impact around addition sites may be more acute but is specific to the mineral and technology. The alkalinity of the ocean increases naturally because of rock weathering in which >1.5 mol of carbon are removed from the atmosphere for every mole of magnesium or calcium dissolved from silicate minerals (e.g., wollastonite, olivine, and anorthite) and 0.5 mol for carbonate minerals (e.g., calcite and dolomite). These processes are responsible for naturally sequestering 0.5 billion tons of CO2 per year. Alkalinity is reduced in the ocean through carbonate mineral precipitation, which is almost exclusively formed from biological activity. Most of the previous work on the biological response to changes in carbonate chemistry have focused on acidifying conditions. More research is required to understand carbonate precipitation at elevated alkalinity to constrain the longevity of carbon storage. A range of technologies have been proposed to increase ocean alkalinity (accelerated weathering of limestone, enhanced weathering, electrochemical promoted weathering, and ocean liming), the cost of which may be comparable to alternative carbon sequestration proposals (e.g., $20-100 tCO2-1). There are still many

Mechanisms of aqueous wollastonite carbonation as a possible CO2 sequestration process

NARCIS (Netherlands)

Huijgen, W.J.J.; Witkamp, G.J.; Comans, R.N.J.

2006-01-01

The mechanisms of aqueous wollastonite carbonation as a possible carbon dioxide sequestration process were investigated experimentally by systematic variation of the reaction temperature, CO2 pressure, particle size, reaction time, liquid to solid ratio and agitation power. The carbonation reaction

CO{sub 2} emissions abatement and geologic sequestration - industrial innovations and stakes - status of researches in progress; Reduction des emissions et stockage geologique du CO{sub 2} - innovation et enjeux industriels - le point des recherches en cours

Energy Technology Data Exchange (ETDEWEB)

NONE

2005-07-01

This colloquium was jointly organized by the French institute of petroleum (IFP), the French agency of environmental and energy mastery (Ademe) and the geological and mining research office (BRGM). This press kit makes a status of the advances made in CO{sub 2} emissions abatement and geological sequestration: technological advances of CO{sub 2} capture and sequestration, geological reservoir dimensioning with respect to the problem scale, duration of such an interim solution, CO{sub 2} emissions abatement potentialities of geological sequestration, regulatory, economical and financial implications, international stakes of greenhouse gas emissions. This press kit comprises a press release about the IFP-Ademe-BRGM colloquium, a slide presentation about CO{sub 2} abatement and sequestration, and four papers: a joint IFP-Ademe-BRGM press conference, IFP's answers to CO{sub 2} emissions abatement, Ademe's actions in CO{sub 2} abatement and sequestration, and BRGM's experience in CO{sub 2} sequestration and climatic change expertise. (J.S.)

Studies on enhancing carbon sequestration in soils

International Nuclear Information System (INIS)

Marland, G.; Garten, C.T.; Post, W.M.; West, T.O.

2004-01-01

Studies of carbon and nitrogen dynamics in ecosystems are leading to an understanding of the factors and mechanisms that affect the inputs to and outputs from soils and how these might be manipulated to enhance C sequestration. Both the quantity and the quality of soil C inputs influence C storage and the potential for C sequestration. Changes in tillage intensity and crop rotations can also affect C sequestration by changing the soil physical and biological conditions and by changing the amounts and types of organic inputs to the soil. Analyses of changes in soil C and N balances are being supplemented with studies of the management practices needed to manage soil carbon and the implications for fossil-fuel use, emission of other greenhouse gases (such as N 2 O and CH 4 ), and impacts on agricultural productivity. The Consortium for Research on Enhancing Carbon Sequestration in Terrestrial Ecosystems (CSiTE) was created in 1999 to perform fundamental research that will lead to methods to enhance C sequestration as one component of a C management strategy. Research to date at one member of this consortium, Oak Ridge National Laboratory, has focused on C sequestration in soils and we begin here to draw together some of the results

Exergy Analysis of a Syngas-Fueled Combined Cycle with Chemical-Looping Combustion and CO2 Sequestration

Directory of Open Access Journals (Sweden)

Álvaro Urdiales Montesino

2016-08-01

Full Text Available Fossil fuels are still widely used for power generation. Nevertheless, it is possible to attain a short- and medium-term substantial reduction of greenhouse gas emissions to the atmosphere through a sequestration of the CO2 produced in fuels’ oxidation. The chemical-looping combustion (CLC technique is based on a chemical intermediate agent, which gets oxidized in an air reactor and is then conducted to a separated fuel reactor, where it oxidizes the fuel in turn. Thus, the oxidation products CO2 and H2O are obtained in an output flow in which the only non-condensable gas is CO2, allowing the subsequent sequestration of CO2 without an energy penalty. Furthermore, with shrewd configurations, a lower exergy destruction in the combustion chemical transformation can be achieved. This paper focus on a second law analysis of a CLC combined cycle power plant with CO2 sequestration using syngas from coal and biomass gasification as fuel. The key thermodynamic parameters are optimized via the exergy method. The proposed power plant configuration is compared with a similar gas turbine system with a conventional combustion, finding a notable increase of the power plant efficiency. Furthermore, the influence of syngas composition on the results is investigated by considering different H2-content fuels.

Negative CO2 emissions via subsurface mineral carbonation in fractured peridotite

Science.gov (United States)

Kelemen, P. B.; Matter, J.

2014-12-01

Uptake of CO2 from surface water via mineral carbonation in peridotite can be engineered to achieve negative CO2 emissions. Reaction with peridotite, e.g., CO2 + olivine (A), serpentine (B) and brucite (C), forms inert, non-toxic, solid carbonates such as magnesite. Experimental studies show that A can be 80% complete in a few hours with 30 micron powders and elevated P(CO2) [1,2,3]. B is slower, but in natural systems the rate of B+C is significant [4]. Methods for capture of dilute CO2 via mineral carbonation [4,5,6,7] are not well known, though CO2 storage via mineral carbonation has been discussed for decades [8,9]. Where crushed peridotite is available, as in mine tailings, increased air or water flow could enhance CO2 uptake at a reasonable cost [4,5]. Here we focus on enhancing subsurface CO2 uptake from surface water flowing in fractured peridotite, in systems driven by thermal convection such as geothermal power plants. Return of depleted water to the surface would draw down CO2 from the air [6,7]. CO2 uptake from water, rate limited by flow in input and output wells, could exceed 1000 tons CO2/yr [7]. If well costs minus power sales were 0.1M to 1M and each system lasts 10 years this costs oil industry. Uptake of 1 Gt CO2/yr at 1000 t/well/yr requires 1M wells, comparable to the number of producing oil and gas wells in the USA. Subsurface CO2 uptake could first be applied in coastal, sub-seafloor peridotite with onshore drilling. Sub-seafloor peridotite is extensive off Oman, New Caledonia and Papua New Guinea, with smaller amounts off Spain, Morocco, USA, etc. This would be a regional contribution, used in parallel with other methods elsewhere. To achieve larger scale is conceivable. There is a giant mass of seafloor peridotite along slow-spreading mid-ocean ridges. Could robotic drills enhance CO2 uptake at a reasonable cost, while fabric chimneys transport CO2-depleted water to the sea surface? Does anyone know James Cameron's phone number? [1] O

Acute physiological impacts of CO{sub 2} ocean sequestration on marine animals

Energy Technology Data Exchange (ETDEWEB)

Ishimatsu, A.; Hayashi, M.; Lee, K.S.; Murata, K.; Kumagai, E. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.; Kikkawa, T. [Marine Ecology Research Inst., Chiba (Japan). Central Laboratory; Kita, J. [Research Inst. of Innovative Technology for the Earth, Kyoto (Japan)

2005-07-01

The biological impacts of ocean carbon dioxide (CO{sub 2}) sequestration must be carefully considered before it is implemented as a mitigation strategy. This paper presented details of a study investigating the effects of high CO{sub 2} concentrations on marine fish, lobster, and octopus. The influence of water temperature on the physiological effects of CO{sub 2} was also discussed. In the first part of the study, eggs and larvae of red seabream were exposed to both CO{sub 2} and HCI-acidified seawater at identical pH levels. Seabream in the CO{sub 2} group showed a much higher mortality rate than fish in the HCI group. Other tests showed that Japanese Flounder died after complete recovery of pH in seawater equilibrated with 5 per cent CO{sub 2}. Cardiac output was rapidly depressed in Yellowtail fish without significant changes in blood oxygen concentrations. Lower temperatures resulted in higher mortality and delayed pH recovery during hypercapnia in all fish. Western rock lobsters were the most tolerant to CO{sub 2} among all species tested. The recovery of hemolymph pH was complete at exposure to CO{sub 2} concentrations of 1 per cent. Changes in hemolymph bicarbonate concentrations indicated that acid-based regulatory mechanisms differed between fish and lobsters. Mortality rates for octopus were significant at CO{sub 2} concentrations of 1 per cent. The results of all tests showed that aquatic animals are more susceptible to increases in ambient CO{sub 2} levels than terrestrial animals. It was concluded that even slight elevations in CO{sub 2} concentration levels adversely affected physiological functioning in the tested species. It was concluded that CO{sub 2} sequestration in deeper, colder waters will have a more pronounced effect on aquatic animals due to the interactions between CO{sub 2} and lower temperatures, as well as the fact that most deep-sea fish are less tolerant to environmental perturbations. 3 refs., 1 tab., 3 figs.

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.)

Increasing CO2 storage in oil recovery

International Nuclear Information System (INIS)

Jessen, K.; Kovscek, A.R.; Orr, F.M. Jr.

2005-01-01

Oil fields offer a significant potential for storing CO 2 and will most likely be the first large scale geological targets for sequestration as the infrastructure, experience and permitting procedures already exist. The problem of co-optimizing oil production and CO 2 storage differs significantly from current gas injection practice due to the cost-benefit imbalance resulting from buying CO 2 for enhanced oil recovery projects. Consequently, operators aim to minimize the amount of CO 2 required to sweep an oil reservoir. For sequestration purposes, where high availability of low cost CO 2 is assumed, the design parameters of enhanced oil recovery processes must be re-defined to optimize the amount of CO 2 left in the reservoir at the time of abandonment. To redefine properly the design parameters, thorough insight into the mechanisms controlling the pore scale displacement efficiency and the overall sweep efficiency is essential. We demonstrate by calculation examples the different mechanisms controlling the displacement behavior of CO 2 sequestration schemes, the interaction between flow and phase equilibrium and how proper design of the injection gas composition and well completion are required to co-optimize oil production and CO 2 storage. [Author

Increasing CO2 storage in oil recovery

International Nuclear Information System (INIS)

Jessen, Kristian; Kovscek, Anthony R.; Orr, Franklin M.

2005-01-01

Oil fields offer a significant potential for storing CO 2 and will most likely be the first large scale geological targets for sequestration as the infrastructure, experience and permitting procedures already exist. The problem of co-optimizing oil production and CO 2 storage differs significantly from current gas injection practice due to the cost-benefit imbalance resulting from buying CO 2 for enhanced oil recovery projects. Consequently, operators aim to minimize the amount of CO 2 required to sweep an oil reservoir. For sequestration purposes, where high availability of low cost CO 2 is assumed, the design parameters of enhanced oil recovery processes must be re-defined to optimize the amount of CO 2 left in the reservoir at the time of abandonment. To redefine properly the design parameters, thorough insight into the mechanisms controlling the pore scale displacement efficiency and the overall sweep efficiency is essential. We demonstrate by calculation examples the different mechanisms controlling the displacement behavior of CO 2 sequestration schemes, the interaction between flow and phase equilibrium and how proper design of the injection gas composition and well completion are required to co-optimize oil production and CO 2 storage

Effect of iron cation on geochemical trapping of CO2 in brine

Science.gov (United States)

Liu, Qi; Maroto-Valer, Mercedes

2014-05-01

Carbon dioxide sequestration using brines has emerged as a promising technology to mitigate the adverse impacts of climate change due to its large storage capacity and favorable chemistries. However, the permanent storage (mineral trapping) of CO2 in brines takes significantly long periods of time as the formation and precipitation of carbonates is very slow .[1]. The main parameters reported to effect on mineral trapping of CO2 sequestration in brines are brine composition, brine pH, system temperature and pressure.[2, 3]. It is suggested that the precipitation of mineral carbonates is mostly dependent on brine pH. Previous studies by the authors concluded that iron in natural brines causes pH instability, but it was not ascertained whether ferric iron or ferrous iron caused pH instability .[4]. Accordingly, the aim of this project is to study synthetic brines mimicking the major ions found in natural brines and including different concentrations of ferric and ferrous iron. Three brines were prepared, as follows: Brine 1 was prepared with ferric Fe3+ iron, Brine 2 prepared with ferrous Fe2+ iron and Brine 3 prepared with no iron. A series of pH stability studies and carbonation reactions were conducted using the above three brines. It is concluded that the ferrous iron causes pH instability, while ferric iron might promote carbonate precipitation. .1. Garcia, S., et al., Sequestration of non-pure carbon dioxide streams in iron oxyhydroxide-containing saline repositories. International Journal of Greenhouse Gas Control, 2012. 7: p. 89-97. 2. Liu, Q. and M.M. Maroto-Valer, Investigation of the pH effect of a typical host rock and buffer solution on CO 2 sequestration in synthetic brines. Fuel Processing Technology, 2010. 91(10): p. 1321-1329. 3. Liu, Q. and M.M. MarotoValer, Parameters affecting mineral trapping of CO2 sequestration in brines. Greenhouse Gases: Science and Technology, 2011. 1(3): p. 211-222. 4. Druckenmiller, M.L. and M.M. Maroto-Valer, Carbon

Maintenance of a living understory enhances soil carbon sequestration in subtropical orchards.

Science.gov (United States)

Liu, Zhanfeng; Lin, Yongbiao; Lu, Hongfang; Ding, Mingmao; Tan, Yaowen; Xu, Shejin; Fu, Shenglei

2013-01-01

Orchard understory represents an important component of the orchards, performing numerous functions related to soil quality, water relations and microclimate, but little attention has been paid on its effect on soil C sequestration. In the face of global climate change, fruit producers also require techniques that increase carbon (C) sequestration in a cost-effective manner. Here we present a case study to compare the effects of understory management (sod culture vs. clean tillage) on soil C sequestration in four subtropical orchards. The results of a 10-year study indicated that the maintenance of sod significantly enhanced the soil C stock in the top 1 m of orchard soils. Relative to clean tillage, sod culture increased annual soil C sequestration by 2.85 t C ha(-1), suggesting that understory management based on sod culture offers promising potential for soil carbon sequestration. Considering that China has the largest area of orchards in the world and that few of these orchards currently have sod understories, the establishment and maintenance of sod in orchards can help China increase C sequestration and greatly contribute to achieving CO2 reduction targets at a regional scale and potentially at a national scale.

Enhanced oil recovery & carbon sequestration building on successful experience

Energy Technology Data Exchange (ETDEWEB)

Stern, Fred [BEPC (United States)

2008-07-15

In this paper it is spoken of the experiences in the capture and sequestration of CO{sub 2} in the companies Basin Electric Power Cooperative (BEPC) and Dakota Gasification Company (DGC); their by-products are mentioned and what these companies are making to control the CO{sub 2} emissions. Their challenges to compress CO{sub 2} are presented and how they have reduced the CO{sub 2} emissions in the DGC of the 2000 to the 2008; how they use CO{sub 2} to enhance the oil recovery and which are their challenges in the CO{sub 2} transport. [Spanish] En esta ponencia se habla de las experiencias en la captura y secuestro de CO{sub 2} en las empresas Basin Electic Power Cooperative (BEPC) y Dakota Gasification Campany (DGC); se mencionan sus subproductos y que estan haciendo estas empresas para controlar las emisiones de CO{sub 2}. Se presentan sus retos para comprimir CO{sub 2} y como han reducido las emisiones de CO{sub 2} en la DGC del 2000 al 2008; como utilizan el CO{sub 2} para mejorar la recuperacion de petroleo y sus cuales son retos en el transporte de CO{sub 2}.

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

Energy Technology Data Exchange (ETDEWEB)

Dr. T. Nakamura; Dr. Miguel Olaizola; Dr. Stephen M. Masutani

2002-12-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO{sub 2} from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report covers the reporting period 1 July to 30 September 2002 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on feasibility demonstration of direct feeding of coal combustion gas to microalgae. Aquasearch continued their effort on selection and characterization of microalgae suitable for CO{sub 2} sequestration. University of Hawaii continued effort on system optimization of the CO{sub 2} sequestration system.

RECOVERY AND SEQUESTRATION OF CO2 FROM STATIONARY COMBUSTION SYSTEMS BY PHOTOSYNTHESIS OF MICROALGAE

Energy Technology Data Exchange (ETDEWEB)

Dr. Takashi Nakamura

2003-04-01

Most of the anthropogenic emissions of carbon dioxide result from the combustion of fossil fuels for energy production. Photosynthesis has long been recognized as a means, at least in theory, to sequester anthropogenic carbon dioxide. Aquatic microalgae have been identified as fast growing species whose carbon fixing rates are higher than those of land-based plants by one order of magnitude. Physical Sciences Inc. (PSI), Aquasearch, and the Hawaii Natural Energy Institute at the University of Hawaii are jointly developing technologies for recovery and sequestration of CO{sub 2} from stationary combustion systems by photosynthesis of microalgae. The research is aimed primarily at demonstrating the ability of selected species of microalgae to effectively fix carbon from typical power plant exhaust gases. This report covers the reporting period 1 October to 31 December 2002 in which PSI, Aquasearch and University of Hawaii conducted their tasks. Based on the work conducted during the previous reporting period, PSI initiated work on feasibility demonstration of direct feeding of coal combustion gas to microalgae. Aquasearch continued their effort on selection and characterization of microalgae suitable for CO{sub 2} sequestration. University of Hawaii continued effort on system optimization of the CO{sub 2} sequestration system.

Big Sky Carbon Sequestration Partnership

Energy Technology Data Exchange (ETDEWEB)

Susan Capalbo

2005-12-31

has significant potential to sequester large amounts of CO{sub 2}. Simulations conducted to evaluate mineral trapping potential of mafic volcanic rock formations located in the Idaho province suggest that supercritical CO{sub 2} is converted to solid carbonate mineral within a few hundred years and permanently entombs the carbon. Although MMV for this rock type may be challenging, a carefully chosen combination of geophysical and geochemical techniques should allow assessment of the fate of CO{sub 2} in deep basalt hosted aquifers. Terrestrial carbon sequestration relies on land management practices and technologies to remove atmospheric CO{sub 2} where it is stored in trees, plants, and soil. This indirect sequestration can be implemented today and is on the front line of voluntary, market-based approaches to reduce CO{sub 2} emissions. Initial estimates of terrestrial sinks indicate a vast potential for increasing and maintaining soil Carbon (C) on rangelands, and forested, agricultural, and reclaimed lands. Rangelands can store up to an additional 0.05 mt C/ha/yr, while the croplands are on average four times that amount. Estimates of technical potential for soil sequestration within the region in cropland are in the range of 2.0 M mt C/yr over 20 year time horizon. This is equivalent to approximately 7.0 M mt CO{sub 2}e/yr. The forestry sinks are well documented, and the potential in the Big Sky region ranges from 9-15 M mt CO{sub 2} equivalent per year. Value-added benefits include enhanced yields, reduced erosion, and increased wildlife habitat. Thus the terrestrial sinks provide a viable, environmentally beneficial, and relatively low cost sink that is available to sequester C in the current time frame. The Partnership recognizes the critical importance of measurement, monitoring, and verification technologies to support not only carbon trading but all policies and programs that DOE and other agencies may want to pursue in support of GHG mitigation. The efforts

Development of Protective Coatings for Co-Sequestration Processes and Pipelines

Energy Technology Data Exchange (ETDEWEB)

Bierwagen, Gordon; Huang, Yaping

2011-11-30

The program, entitled Development of Protective Coatings for Co-Sequestration Processes and Pipelines, examined the sensitivity of existing coating systems to supercritical carbon dioxide (SCCO2) exposure and developed new coating system to protect pipelines from their corrosion under SCCO2 exposure. A literature review was also conducted regarding pipeline corrosion sensors to monitor pipes used in handling co-sequestration fluids. Research was to ensure safety and reliability for a pipeline involving transport of SCCO2 from the power plant to the sequestration site to mitigate the greenhouse gas effect. Results showed that one commercial coating and one designed formulation can both be supplied as potential candidates for internal pipeline coating to transport SCCO2.

Mechanisms of aqueous wollastonite carbonation as a possible CO2 sequestration process

International Nuclear Information System (INIS)

Huijgen, W.J.J.; Comans, R.N.J.; Witkamp, G.J.

2006-02-01

The mechanisms of aqueous wollastonite carbonation as a possible carbon dioxide sequestration process were investigated experimentally by systematic variation of the reaction temperature, CO2 pressure, particle size, reaction time, liquid to solid ratio and agitation power. The carbonation reaction was observed to occur via the aqueous phase in two steps: (1) Ca leaching from the CaSiO3 matrix and (2) CaCO3 nucleation and growth. Leaching is hindered by a Ca-depleted silicate rim resulting from incongruent Ca-dissolution. Two temperature regimes were identified in the overall carbonation process. At temperatures below an optimum reaction temperature, the overall reaction rate is probably limited by the leaching rate of Ca. At higher temperatures, nucleation and growth of calcium carbonate is probably limiting the conversion, due to a reduced (bi)carbonate activity. The mechanisms for the aqueous carbonation of wollastonite were shown to be similar to those reported previously for an industrial residue and a Mg-silicate. The carbonation of wollastonite proceeds rapidly relative to Mg-silicates, with a maximum conversion in 15 min of 70% at 200C, 20 bar CO2 partial pressure and a particle size of <38 μm. The obtained insight in the reaction mechanisms enables the energetic and economic assessment of CO2 sequestration by wollastonite carbonation, which forms an essential next step in its further development

Workshop on capture and sequestration of CO{sub 2} (CCS); Taller sobre captura y secuestro de CO{sub 2} (CCS)

Energy Technology Data Exchange (ETDEWEB)

NONE

2008-07-15

In this workshop diverse communications related to the capture and sequestration of CO{sub 2} are presented. This workshop was realized in the Technological Museum of the Comision Federal de Electricidad (CFE), in Mexico City on the ninth and tenth of July, 2008, and it had the objective of reflecting the necessity of considering in Mexico the application of the capture and sequestration technologies of CO{sub 2} (CCS), as well as to put in touch the technicians and managers of the Mexican institutions with the world-wide leaders in these technologies and with the managers of companies that are successfully applying CCS technologies. [Spanish] En este taller se presentan diversas ponencias relacionadas con la captura y secuestro de CO{sub 2}. Este taller se realizo en el Museo Tecnologico de la Comision Federal de Electricidad (CFE), en la Ciudad de Mexico, los dias 9 y 10 de julio de 2008 y tuvo como objetivo reflexionar sobre la necesidad de considerar en Mexico, la aplicacion de las tecnologias de captura y secuestro de CO{sub 2} (CCS), asi como poner en contacto a los tecnicos y directivos de las instituciones mexicanas con los lideres mundiales en estas tecnologias y con los directivos de empresas que estan aplicando con exito tecnologias de CCS.

CO{sub 2} Energy Reactor – Integrated Mineral Carbonation: Perspectives on Lab-Scale Investigation and Products Valorization

Energy Technology Data Exchange (ETDEWEB)

Santos, Rafael M., E-mail: rafael.santos@alumni.utoronto.ca [Chemical and Environmental Laboratories (CEL), School of Applied Chemical and Environmental Sciences, Sheridan Institute of Technology, Brampton, ON (Canada); Knops, Pol C. M.; Rijnsburger, Keesjan L. [Innovation Concepts B.V., Twello (Netherlands); Chiang, Yi Wai [School of Engineering, University of Guelph, Guelph, ON (Canada)

2016-02-15

To overcome the challenges of mineral CO{sub 2} sequestration, Innovation Concepts B.V. is developing a unique proprietary gravity pressure vessel (GPV) reactor technology and has focussed on generating reaction products of high economic value. The GPV provides intense process conditions through hydrostatic pressurization and heat exchange integration that harvests exothermic reaction energy, thereby reducing energy demand of conventional reactor designs, in addition to offering other benefits. In this paper, a perspective on the status of this technology and outlook for the future is provided. To date, laboratory-scale tests of the envisioned process have been performed in a tubular “rocking autoclave” reactor. The mineral of choice has been olivine [~Mg{sub 1.6}Fe{sup 2+}{sub 0.4}(SiO{sub 4}) + ppm Ni/Cr], although asbestos, steel slags, and oil shale residues are also under investigation. The effect of several process parameters on reaction extent and product properties has been tested: CO{sub 2} pressure, temperature, residence time, additives (buffers, lixiviants, chelators, oxidizers), solids loading, and mixing rate. The products (carbonates, amorphous silica, and chromite) have been physically separated (based on size, density, and magnetic properties), characterized (for chemistry, mineralogy, and morphology), and tested in intended applications (as pozzolanic carbon-negative building material). Economically, it is found that product value is the main driver for mineral carbonation, rather than, or in addition to, the sequestered CO{sub 2}. The approach of using a GPV and focusing on valuable reaction products could thus make CO{sub 2} mineralization a feasible and sustainable industrial process.

The sequestration switch. Removing industrial CO2 by direct ocean absorption

International Nuclear Information System (INIS)

Ametistova, Lioudmila; Briden, James; Twidell, John

2002-01-01

This review paper considers direct injection of industrial CO 2 emissions into the mid-water oceanic column below 500 m depth. Such a process is a potential candidate for switching atmospheric carbon emissions directly to long term sequestration, thereby relieving the intermediate atmospheric burden. Given sufficient research justification, the argument is that harmful impact in both the Atmosphere and the biologically rich upper marine layer could be reduced. The paper aims to estimate the role that active intervention, through direct ocean CO 2 storage, could play and to outline further research and assessment for the strategy to be a viable option for climate change mitigation. The attractiveness of direct ocean injection lies in its bypassing of the Atmosphere and upper marine region, its relative permanence, its practicability using existing technologies and its quantification. The difficulties relate to the uncertainty of some fundamental scientific issues, such as plume dynamics, lowered pH of the exposed waters and associated ecological impact, the significant energy penalty associated with the necessary engineering plant and the uncertain costs. Moreover, there are considerable uncertainties regarding related international marine law. Development of the process would require acceptance of the evidence for climate change, strict requirements for large industrial consumers of fossil fuel to reduce CO 2 emissions into the Atmosphere and scientific evidence for the overall beneficial impact of ocean sequestration

In-Situ MVA of CO₂ Sequestration Using Smart Field Technology

Energy Technology Data Exchange (ETDEWEB)

Mohaghegh, Shahab D. [West Virginia Univ. Research Corporation, Morgantown, WV (United States)

2014-09-01

Capability of underground carbon dioxide storage to confine and sustain injected CO₂ for a long period of time is the main concern for geologic CO₂ sequestration. If a leakage from a geological CO₂ sequestration site occurs, it is crucial to find the approximate amount and the location of the leak, in a timely manner, in order to implement proper remediation activities. An overwhelming majority of research and development for storage site monitoring has been concentrated on atmospheric, surface or near surface monitoring of the sequestered CO₂ . This study aims to monitor the integrity of CO₂ storage at the reservoir level. This work proposes developing in-situ CO₂ Monitoring and Verification technology based on the implementation of Permanent Down-hole Gauges (PDG) or “Smart Wells” along with Artificial Intelligence and Data Mining (AI&DM). The technology attempts to identify the characteristics of the CO₂ leakage by de-convolving the pressure signals collected from Permanent Down-hole Gauges (PDG). Citronelle field, a saline aquifer reservoir, located in the U.S. was considered as the basis for this study. A reservoir simulation model for CO₂ sequestration in the Citronelle field was developed and history matched. PDGs were installed, and therefore were considered in the numerical model, at the injection well and an observation well. Upon completion of the history matching process, high frequency pressure data from PDGs were generated using the history matched numerical model using different CO₂ leakage scenarios. Since pressure signal behaviors were too complicated to de-convolute using any existing mathematical formulations, a Machine Learning-based technology was introduced for this purpose. An Intelligent Leakage Detection System (ILDS) was developed as the result of this effort using the machine learning and pattern recognition technologies. The ILDS

Comprehensive, Quantitative Risk Assessment of CO{sub 2} Geologic Sequestration

Energy Technology Data Exchange (ETDEWEB)

Lepinski, James

2013-09-30

A Quantitative Failure Modes and Effects Analysis (QFMEA) was developed to conduct comprehensive, quantitative risk assessments on CO{sub 2} capture, transportation, and sequestration or use in deep saline aquifers, enhanced oil recovery operations, or enhanced coal bed methane operations. The model identifies and characterizes potential risks; identifies the likely failure modes, causes, effects and methods of detection; lists possible risk prevention and risk mitigation steps; estimates potential damage recovery costs, mitigation costs and costs savings resulting from mitigation; and ranks (prioritizes) risks according to the probability of failure, the severity of failure, the difficulty of early failure detection and the potential for fatalities. The QFMEA model generates the necessary information needed for effective project risk management. Diverse project information can be integrated into a concise, common format that allows comprehensive, quantitative analysis, by a cross-functional team of experts, to determine: What can possibly go wrong? How much will damage recovery cost? How can it be prevented or mitigated? What is the cost savings or benefit of prevention or mitigation? Which risks should be given highest priority for resolution? The QFMEA model can be tailored to specific projects and is applicable to new projects as well as mature projects. The model can be revised and updated as new information comes available. It accepts input from multiple sources, such as literature searches, site characterization, field data, computer simulations, analogues, process influence diagrams, probability density functions, financial analysis models, cost factors, and heuristic best practices manuals, and converts the information into a standardized format in an Excel spreadsheet. Process influence diagrams, geologic models, financial models, cost factors and an insurance schedule were developed to support the QFMEA model. Comprehensive, quantitative risk assessments

CO2 sequestration in two mediterranean dune areas subjected to a different level of anthropogenic disturbance

Science.gov (United States)

Bonito, Andrea; Ricotta, Carlo; Iberite, Mauro; Gratani, Loretta; Varone, Laura

2017-09-01

Coastal sand dunes are among the most threatened habitats, especially in the Mediterranean Basin, where the high levels of human pressure impair the presence of plant species, putting at risk the maintenance of the ecosystem services, such as CO2 sequestration provided by these habitats. The aim of this study was to analyze how disturbance-induced changes in plant species abundance patterns account for variations in annual CO2 sequestration flow (CS) of Mediterranean sand dune areas. Two sites characterized by a high (site HAD) and a lower (site LAD) anthropogenic disturbance level were selected. At both sites, plant species number, cover, height and CS based on net photosynthesis measurements were sampled. At the plant species level, our results highlighted that Ammophila arenaria and Pancratium maritimum, had a key role in CS. Moreover, the results revealed a patchy species assemblage in both sites. In particular, HAD was characterized by a higher extension of the anthropogenic aphytoic zone (64% of the total transect length) than LAD. In spite of the observed differences in plant species composition, there were not significant differences between HAD and LAD in structural and functional traits, such as plant height and net photosynthesis. As a consequence, HAD and LAD had a similar CS (443 and 421 Mg CO2 ha-1 y-1, respectively). From a monetary point of view, our estimates based on the social costs of carbon revealed that the flow of sequestered CO2 valued on an average 3181 ± 114 ha-1 year-1 (mean value for the two sites). However, considering also the value of the CO2 negative flow related to loss of vegetated area, the annual net benefit arising from CO2 sequestration amounted to 1641 and 1772 for HAD and LAD, respectively. Overall, the results highlighted the importance to maximize the efforts to preserve dune habitats by applying an effective management policy, which could allow maintaining also a regulatory ecosystem service such as CO2 sequestration.

Effects of mineral additives on biochar formation: carbon retention, stability, and properties.

Science.gov (United States)

Li, Feiyue; Cao, Xinde; Zhao, Ling; Wang, Jianfei; Ding, Zhenliang

2014-10-07

Biochar is being recognized as a promising tool for long-term carbon sequestration, and biochar with high carbon retention and strong stability is supposed to be explored for that purpose. In this study, three minerals, including kaolin, calcite (CaCO3), and calcium dihydrogen phosphate [Ca(H2PO4)2], were added to rice straw feedstock at the ratio of 20% (w/w) for biochar formation through pyrolysis treatment, aiming to improve carbon retention and stabilization in biochar. Kaolin and CaCO3 had little effect on the carbon retention, whereas Ca(H2PO4)2 increased the carbon retention by up to 29% compared to untreated biochar. Although the carbon loss from the kaolin-modified biochar with hydrogen peroxide oxidation was enhanced, CaCO3 and Ca(H2PO4)2 modification reduced the carbon loss by 18.6 and 58.5%, respectively. Moreover, all three minerals reduced carbon loss of biochar with potassium dichromate oxidation from 0.3 to 38.8%. The microbial mineralization as CO2 emission in all three modified biochars was reduced by 22.2-88.7% under aerobic incubation and 5-61% under anaerobic incubation. Enhanced carbon retention and stability of biochar with mineral treatment might be caused by the enhanced formation of aromatic C, which was evidenced by cross-polarization magic angle spinning (13)C nuclear magnetic resonance spectra and Fourier transform infrared spectroscopy analysis. Our results indicated that the three minerals, especially Ca(H2PO4)2, were effective in increasing carbon retention and strengthening biochar stabilization, which provided a novel idea that people could explore and produce the designated biochar with high carbon sequestration capacity and stability.

How much CO2 is trapped in carbonate minerals of a natural CO2 occurrence?

Science.gov (United States)

Király, Csilla; Szabó, Zsuzsanna; Szamosfalvi, Ágnes; Cseresznyés, Dóra; Király, Edit; Szabó, Csaba; Falus, György

2017-04-01

Carbon Capture and Storage (CCS) is a transitional technology to decrease CO2 emissions from human fossil fuel usage and, therefore, to mitigate climate change. The most important criteria of a CO2 geological storage reservoir is that it must hold the injected CO2 for geological time scales without its significant seepage. The injected CO2 undergoes physical and chemical reactions in the reservoir rocks such as structural-stratigraphic, residual, dissolution or mineral trapping mechanisms. Among these, the safest is the mineral trapping, when carbonate minerals such as calcite, ankerite, siderite, dolomite and dawsonite build the CO2 into their crystal structures. The study of natural CO2 occurrences may help to understand the processes in CO2 reservoirs on geological time scales. This is the reason why the selected, the Mihályi-Répcelak natural CO2 occurrence as our research area, which is able to provide particular and highly significant information for the future of CO2 storage. The area is one of the best known CO2 fields in Central Europe. The main aim of this study is to estimate the amount of CO2 trapped in the mineral phase at Mihályi-Répcelak CO2 reservoirs. For gaining the suitable data, we apply petrographic, major and trace element (microprobe and LA-ICP-MS) and stable isotope analysis (mass spectrometry) and thermodynamic and kinetic geochemical models coded in PHREEQC. Rock and pore water compositions of the same formation, representing the pre-CO2 flooding stages of the Mihályi-Répcelak natural CO2 reservoirs are used in the models. Kinetic rate parameters are derived from the USGS report of Palandri and Kharaka (2004). The results of petrographic analysis show that a significant amount of dawsonite (NaAlCO3(OH)2, max. 16 m/m%) precipitated in the rock due to its reactions with CO2 which flooded the reservoir. This carbonate mineral alone traps about 10-30 kg/m3 of the reservoir rock from the CO2 at Mihályi-Répcelak area, which is an

Assessment of CO2 Mineralization and Dynamic Rock Properties at the Kemper Pilot CO2 Injection Site

Science.gov (United States)

Qin, F.; Kirkland, B. L.; Beckingham, L. E.

2017-12-01

CO2-brine-mineral reactions following CO2 injection may impact rock properties including porosity, permeability, and pore connectivity. The rate and extent of alteration largely depends on the nature and evolution of reactive mineral interfaces. In this work, the potential for geochemical reactions and the nature of the reactive mineral interface and corresponding hydrologic properties are evaluated for samples from the Lower Tuscaloosa, Washita-Fredericksburg, and Paluxy formations. These formations have been identified as future regionally extensive and attractive CO2 storage reservoirs at the CO2 Storage Complex in Kemper County, Mississippi, USA (Project ECO2S). Samples from these formations were obtained from the Geological Survey of Alabama and evaluated using a suite of complementary analyses. The mineral composition of these samples will be determined using petrography and powder X-ray Diffraction (XRD). Using these compositions, continuum-scale reactive transport simulations will be developed and the potential CO2-brine-mineral interactions will be examined. Simulations will focus on identifying potential reactive minerals as well as the corresponding rate and extent of reactions. The spatial distribution and accessibility of minerals to reactive fluids is critical to understanding mineral reaction rates and corresponding changes in the pore structure, including pore connectivity, porosity and permeability. The nature of the pore-mineral interface, and distribution of reactive minerals, will be determined through imaging analysis. Multiple 2D scanning electron microscopy (SEM) backscattered electron (BSE) images and energy dispersive x-ray spectroscopy (EDS) images will be used to create spatial maps of mineral distributions. These maps will be processed to evaluate the accessibility of reactive minerals and the potential for flow-path modifications following CO2 injection. The "Establishing an Early CO2 Storage Complex in Kemper, MS" project is funded by

Development of suitable photobioreactors for CO{sub 2} sequestration addressing global warming using green algae and cyanobacteria

Energy Technology Data Exchange (ETDEWEB)

Kumar, K.; Dasgupta, C.N.; Nayak, B.; Lindblad, P.; Das, D. [Indian Institute of Technology, Kharagpur (India)

2011-04-15

CO{sub 2} sequestration by cyanobacteria and green algae are receiving increased attention in alleviating the impact of increasing CO{sub 2} in the atmosphere. They, in addition to CO{sub 2} capture, can produce renewable energy carriers such as carbon free energy hydrogen, bioethanol, biodiesel and other valuable biomolecules. Biological fixation of CO{sub 2} are greatly affected by the characteristics of the microbial strains, their tolerance to temperature and the CO{sub 2} present in the flue gas including SOx, NOx. However, there are additional factors like the availability of light, pH, O{sub 2}, removal, suitable design of the photobioreactor, culture density and the proper agitation of the reactor that will affect significantly the CO{sub 2} sequestration process. Present paper deals with the photobioreactors of different geometry available for biomass production. It also focuses on the hybrid types of reactors (integrating two reactors) which can be used for overcoming the bottlenecks of a single photobioreactor.

Carbon dioxide sequestration: Modeling the diffusive and convective transport under a CO2 cap

KAUST Repository

Allen, Rebecca

2012-01-01

A rise in carbon dioxide levels from industrial emissions is contributing to the greenhouse effect and global warming. CO2 sequestration in saline aquifers is a strategy to reduce atmospheric CO2 levels. Scientists and researchers rely on numerical simulators to predict CO2 storage by modeling the fluid transport behaviour. Studies have shown that after CO2 is injected into a saline aquifer, undissolved CO2 rises due to buoyant forces and will spread laterally away from the injection site under an area of low permeability. CO2 from this ‘capped\\' region diffuses into the fluid underlying it, and the resulting CO2-fluid mixture increases in density. This increase in density leads to gravity-driven convection. Accordingly, diffusive-convective transport is important to model since it predicts an enhanced storage capacity of the saline aquifer. This work incorporates the diffusive and convective transport processes into the transport modeling equation, and uses a self-generated code. Discretization of the domain is done with a cell-centered finite difference method. Cases are set up using similar parameters from published literature in order to compare results. Enhanced storage capacity is predicted in this work, similar to work done by others. A difference in the onset of convective transport between this work and published results is noticed and discussed in this paper. A sensitivity analysis is performed on the density model used in this work, and on the diffusivity value assumed. The analysis shows that the density model and diffusivity value is a key component on simulation results. Also, perturbations are added to porosity and permeability in order to see the effect of perturbations on the onset of convection, and results agree with similar findings by others. This work provides a basis for studying other cases, such as the impact of heterogeneity on the diffusion-convective transport. An extension of this work may involve the use of an equation of state to

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

Geologic Sequestration of CO2 in Deep, Unmineable Coalbeds: An Integrated Researdh and Commercial-Scale Field Demonstration Project

Energy Technology Data Exchange (ETDEWEB)

Scott Reeves; George Koperna

2008-09-30

The Coal-Seq consortium is a government-industry collaborative consortium with the objective of advancing industry's understanding of complex coalbed methane and gas shale reservoir behavior in the presence of multi-component gases via laboratory experiments, theoretical model development and field validation studies. This will allow primary recovery, enhanced recovery and CO{sub 2} sequestration operations to be commercially enhanced and/or economically deployed. The project was initially launched in 2000 as a U.S. Department of Energy sponsored investigation into CO{sub 2} sequestration in deep, unmineable coalseams. The initial project accomplished a number of important objectives, which mainly revolved around performing baseline experimental studies, documenting and analyzing existing field projects, and establishing a global network for technology exchange. The results from that Phase have been documented in a series of reports which are publicly available. An important outcome of the initial phase was that serious limitations were uncovered in our knowledge of reservoir behavior when CO{sub 2} is injected into coal. To address these limitations, the project was extended in 2005 as a government-industry collaborative consortium. Selected accomplishments from this phase have included the identification and/or development of new models for multi-component sorption and diffusion, laboratory studies of coal geomechanical and permeability behavior with CO{sub 2} injection, additional field validation studies, and continued global technology exchange. Further continuation of the consortium is currently being considered. Some of the topics that have been identified for investigation include further model development/refinement related to multicomponent equations-of-state, sorption and diffusion behavior, geomechanical and permeability studies, technical and economic feasibility studies for major international coal basins, the extension of the work to gas shale

An equivalence factor between CO2 avoided emissions and sequestration. Description and applications in forestry

International Nuclear Information System (INIS)

Costa, P.M.; Wilson, C.

2000-01-01

Concern about the issue of permanence and reversibility of the effects of carbon sequestration has led to the need to devise accounting methods that quantify the temporal value of storing carbon that has been actively sequestered or removed from the atmosphere, as compared to carbon stored as a result of activities taken to avoid emissions. This paper describes a method for accounting for the atmospheric effects of sequestration-based land-use projects in relation to the duration of carbon storage. Firstly, the time period over which sequestered carbon should be stored in order to counteract the radiative forcing effect of carbon emissions was calculated, based on the residence time and decay pattern of atmospheric CO2, its Absolute Global Warming Potential. This time period was called the equivalence time, and was calculated to be approximately 55 years. From this equivalence time, the effect of storage of 1 t CO2 for 1 year was derived, and found to be similar to preventing the effect of the emission of 0.0182 t CO2. Potential applications of this tonne.year figure, here called the equivalence factor, are then discussed in relation to the estimation of atmospheric benefits over time of sequestration-based land use projects. 15 refs

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.

Enhanced Oil Recovery with CO2 Capture and Sequestration

Energy Technology Data Exchange (ETDEWEB)

Andrei, Maria; De Simoni, Michela; Delbianco, Alberto; Cazzani, Piero; Zanibelli, Laura

2010-09-15

This paper presents the results of a feasibility study aimed at extending the production life of a small oilfield in Italy through EOR, employing the CO2 captured from the flue gas streams of the refinery nearby. The EOR operation allows the recovery of additional reserves while a consistent amount of the CO2 injected remains permanently stored into the reservoir. The screening process selection for EOR-CO2 and the main elements of the pilot project for the proper upstream-downstream integration will be described. Evaluation of EOR-CO2 extension to other oilfields and its effect on oil production and project's economics will be reported.

In situ mid-infrared spectroscopic titration of forsterite with water in supercritical CO2: Dependence of mineral carbonation on quantitative water speciation

Science.gov (United States)

Loring, J. S.; Thompson, C. J.; Wang, Z.; Schaef, H. T.; Martin, P.; Qafoku, O.; Felmy, A. R.; Rosso, K. M.

2011-12-01

Geologic sequestration of carbon dioxide holds promise for helping mitigate CO2 emissions generated from the burning of fossil fuels. Supercritical CO2 (scCO2) plumes containing variable water concentrations (wet scCO2) will displace aqueous solution and dominate the pore space adjacent to caprocks. It is important to understand possible mineral reactions with wet scCO2 to better predict long-term caprock integrity. We introduce novel in situ instrumentation that enables quantitative titrations of reactant minerals with water in scCO2 at temperatures and pressures relevant to target geologic reservoirs. The system includes both transmission and attenuated total reflection mid-infrared optics. Transmission infrared spectroscopy is used to measure concentrations of water dissolved in the scCO2, adsorbed on mineral surfaces, and incorporated into precipitated carbonates. Single-reflection attenuated total reflection infrared spectroscopy is used to monitor water adsorption, mineral dissolution, and carbonate precipitation reactions. Results are presented for the infrared spectroscopic titration of forsterite (Mg2SiO4), a model divalent metal silicate, with water in scCO2 at 100 bar and at both 50 and 75°C. The spectral data demonstrate that the quantitative speciation of water as either dissolved or adsorbed is important for understanding the types, growth rates, and amounts of carbonate precipitates formed. Relationships between dissolved/adsorbed water, water concentrations, and the role of liquid-like adsorbed water are discussed. Our results unify previous in situ studies from our laboratory based on infrared spectroscopy, nuclear magnetic resonance spectroscopy and X-ray diffraction.

Downhole fluid injection systems, CO2 sequestration methods, and hydrocarbon material recovery methods

Science.gov (United States)

Schaef, Herbert T.; McGrail, B. Peter

2015-07-28

Downhole fluid injection systems are provided that can include a first well extending into a geological formation, and a fluid injector assembly located within the well. The fluid injector assembly can be configured to inject a liquid CO2/H2O-emulsion into the surrounding geological formation. CO2 sequestration methods are provided that can include exposing a geological formation to a liquid CO2/H2O-emulsion to sequester at least a portion of the CO2 from the emulsion within the formation. Hydrocarbon material recovery methods are provided that can include exposing a liquid CO2/H2O-emulsion to a geological formation having the hydrocarbon material therein. The methods can include recovering at least a portion of the hydrocarbon material from the formation.

Simplified predictive models for CO₂ sequestration performance assessment

Energy Technology Data Exchange (ETDEWEB)

Mishra, Srikanta [Battelle Memorial Inst., Columbus, OH (United States); Ganesh, Priya [Battelle Memorial Inst., Columbus, OH (United States); Schuetter, Jared [Battelle Memorial Inst., Columbus, OH (United States); He, Jincong [Battelle Memorial Inst., Columbus, OH (United States); Jin, Zhaoyang [Battelle Memorial Inst., Columbus, OH (United States); Durlofsky, Louis J. [Battelle Memorial Inst., Columbus, OH (United States)

2015-09-30

CO2 sequestration in deep saline formations is increasingly being considered as a viable strategy for the mitigation of greenhouse gas emissions from anthropogenic sources. In this context, detailed numerical simulation based models are routinely used to understand key processes and parameters affecting pressure propagation and buoyant plume migration following CO2 injection into the subsurface. As these models are data and computation intensive, the development of computationally-efficient alternatives to conventional numerical simulators has become an active area of research. Such simplified models can be valuable assets during preliminary CO2 injection project screening, serve as a key element of probabilistic system assessment modeling tools, and assist regulators in quickly evaluating geological storage projects. We present three strategies for the development and validation of simplified modeling approaches for CO2 sequestration in deep saline formations: (1) simplified physics-based modeling, (2) statisticallearning based modeling, and (3) reduced-order method based modeling. In the first category, a set of full-physics compositional simulations is used to develop correlations for dimensionless injectivity as a function of the slope of the CO2 fractional-flow curve, variance of layer permeability values, and the nature of vertical permeability arrangement. The same variables, along with a modified gravity number, can be used to develop a correlation for the total storage efficiency within the CO2 plume footprint. Furthermore, the dimensionless average pressure buildup after the onset of boundary effects can be correlated to dimensionless time, CO2 plume footprint, and storativity contrast between the reservoir and caprock. In the second category, statistical “proxy models” are developed using the simulation domain described previously with two approaches: (a) classical Box-Behnken experimental design with a quadratic response surface, and (b) maximin

Supercritical Fluid Behavior at Nanoscale Interfaces: Implications for CO2 Sequestration in Geologic Formations

Czech Academy of Sciences Publication Activity Database

Cole, D.R.; Chialvo, A. A.; Rother, G.; Vlček, Lukáš; Cummings, P. T.

2010-01-01

Roč. 90, 17-18 (2010), s. 2329-2363 ISSN 1478-6435 Institutional research plan: CEZ:AV0Z40720504 Keywords : sequestration * nanostructures * supercritical CO2 Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.302, year: 2010

Long-term nitrogen regulation of forest carbon sequestration

Science.gov (United States)

Yang, Y.; Luo, Y.

2009-12-01

It is well established that nitrogen (N) limits plant production but unclear how N regulates long-term terrestrial carbon (C) sequestration in response to rising atmospheric C dioxide (CO2)(Luo et al., 2004). Most experimental evidence on C-N interactions is primarily derived from short-term CO2 manipulative studies (e.g. Oren et al., 2001; Reich et al., 2006a), which abruptly increase C inputs into ecosystems and N demand from soil while atmospheric CO2 concentration in the real world is gradually increasing over time (Luo & Reynolds, 1999). It is essential to examine long-term N regulations of C sequestration in natural ecosystems. Here we present results of a synthesis of more than 100 studies on long-term C-N interactions during secondary succession. C significantly accumulates in plant, litter and forest floor in most studies, and in mineral soil in one-third studies during stand development. Substantial increases in C stock are tightly coupled with N accretion. The C: N ratio in plant increases with stand age in most cases, but remains relatively constant in litter, forest floor and mineral soil. Our results suggest that natural ecosystems could have the intrinsic capacity to maintain long-term C sequestration through external N accrual, high N use efficiency, and efficient internal N cycling.

Exploratory Research on Simulation of CO2-Brine-Mineral Interactions

Energy Technology Data Exchange (ETDEWEB)

Chen Zhu; Shiao hung Chiang

2005-11-01

Application of many carbon sequestration strategies requires knowledge of thermodynamic properties for the extremely complex chemical system of CO{sub 2}-SO{sub 2}-H{sub 2}O-NaCl-CaCl{sub 2}-MgCl{sub 2}. This University Coal Research Phase I program has been successful and highly productive in exploring an approach to develop an equation of state (EOS) to describe thermodynamic properties in the above chemical system. We have compiled available laboratory experimental data and thermodynamic models, and evaluated their appropriateness for the carbon sequestration process. Based on this literature review, we provided an improved CO{sub 2} solubility model for the CO{sub 2}-H{sub 2}O-NaCl system, which incorporates newly available experimental measurements funded by DOE, and is valid in temperature range from 273 to 533 K, pressure from 0 to 2000 bar, and salinity from 0 to 4.5 molality of NaCl equivalent. The improved model also greatly improves the computational efficiency of CO{sub 2} solubility calculations and thus is better suited to be incorporated into large computer simulation models (e.g., reservoir simulation models). The literature review and model development provided insights of the data needs and directions for future work. Synergetic collaboration with DOE scientists has resulted in simulations of injected CO{sub 2} fate in sandstone aquifer with a one-dimensional numerical coupled reactive transport model. We evaluated over 100 references on CO{sub 2} solubility and submitted two manuscripts to peer-reviewed journals. One paper has been accepted for publication in ''Environmental Geosciences''.

Fluid characterization for miscible EOR projects and CO2 sequestration

DEFF Research Database (Denmark)

Jessen, Kristian; Stenby, Erling Halfdan

2007-01-01

Accurate performance prediction of miscible enhanced-oil-recovery (EOR) projects or CO, sequestration in depleted oil and gas reservoirs relies in part on the ability of an equation-of-state (EOS) model to adequately represent the properties of a wide range of mixtures of the resident fluid...... in the data reduction and demonstrate that for some gas/oil systems, swelling tests do not contribute to a more accurate prediction of multicontact miscibility. Finally, we report on the impact that use of EOS models based on different characterization procedures can have on recovery predictions from dynamic...... and the injected fluid(s). The mixtures that form when gas displaces oil in a porous medium will, in many cases, differ significantly from compositions created in swelling tests and other standard pressure/volume/temperature (PVT) experiments. Multicontact experiments (e.g., slimtube displacements) are often used...

Enhanced transport phenomena in CO2 sequestration and CO2 EOR

NARCIS (Netherlands)

Farajzadeh, R.

2009-01-01

The results of this thesis give insight into the (mass)-transfer during flow of gases, especially CO2, in various gas-liquid systems. A number of experiments was performed to investigate the transport phenomena through interfaces with and without surfactant monolayers. The observed phenomena have

Vertical equilibrium with sub-scale analytical methods for geological CO2 sequestration

KAUST Repository

Gasda, S. E.

2009-04-23

Large-scale implementation of geological CO2 sequestration requires quantification of risk and leakage potential. One potentially important leakage pathway for the injected CO2 involves existing oil and gas wells. Wells are particularly important in North America, where more than a century of drilling has created millions of oil and gas wells. Models of CO 2 injection and leakage will involve large uncertainties in parameters associated with wells, and therefore a probabilistic framework is required. These models must be able to capture both the large-scale CO 2 plume associated with the injection and the small-scale leakage problem associated with localized flow along wells. Within a typical simulation domain, many hundreds of wells may exist. One effective modeling strategy combines both numerical and analytical models with a specific set of simplifying assumptions to produce an efficient numerical-analytical hybrid model. The model solves a set of governing equations derived by vertical averaging with assumptions of a macroscopic sharp interface and vertical equilibrium. These equations are solved numerically on a relatively coarse grid, with an analytical model embedded to solve for wellbore flow occurring at the sub-gridblock scale. This vertical equilibrium with sub-scale analytical method (VESA) combines the flexibility of a numerical method, allowing for heterogeneous and geologically complex systems, with the efficiency and accuracy of an analytical method, thereby eliminating expensive grid refinement for sub-scale features. Through a series of benchmark problems, we show that VESA compares well with traditional numerical simulations and to a semi-analytical model which applies to appropriately simple systems. We believe that the VESA model provides the necessary accuracy and efficiency for applications of risk analysis in many CO2 sequestration problems. © 2009 Springer Science+Business Media B.V.

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

Mineralization of Carbon Dioxide: Literature Review

Energy Technology Data Exchange (ETDEWEB)

Romanov, V; Soong, Y; Carney, C; Rush, G; Nielsen, B; O' Connor, W

2015-01-01

CCS research has been focused on CO2 storage in geologic formations, with many potential risks. An alternative to conventional geologic storage is carbon mineralization, where CO2 is reacted with metal cations to form carbonate minerals. Mineralization methods can be broadly divided into two categories: in situ and ex situ. In situ mineralization, or mineral trapping, is a component of underground geologic sequestration, in which a portion of the injected CO2 reacts with alkaline rock present in the target formation to form solid carbonate species. In ex situ mineralization, the carbonation reaction occurs above ground, within a separate reactor or industrial process. This literature review is meant to provide an update on the current status of research on CO2 mineralization. 2

Enhanced CO2 sequestration by a novel microalga: Scenedesmus obliquus SA1 isolated from bio-diversity hotspot region of Assam, India.

Science.gov (United States)

Basu, Samarpita; Roy, Abhijit Sarma; Mohanty, Kaustubha; Ghoshal, Aloke K

2013-09-01

The present study aimed to isolate a high CO2 and temperature tolerant microalga capable of sequestering CO2 from flue gas. Microalga strain SA1 was isolated from a freshwater body of Assam and identified as Scenedesmus obliquus (KC733762). At 13.8±1.5% CO2 and 25 °C, maximum biomass (4.975±0.003 g L(-1)) and maximum CO2 fixation rate (252.883±0.361 mg L(-1) d(-1)) were obtained which were higher than most of the relevant studies. At elevated temperature (40 °C) and 13.8±1.5% CO2 maximum biomass (0.883±0.001 g L(-1)) was obtained. The carbohydrate, protein, lipid, and chlorophyll content of the CO2 treated SA1 were 30.87±0.64%, 9.48±1.65%, 33.04±0.46% and 6.03±0.19% respectively, which were higher than previous reports. Thus, SA1 could prove to be a potential candidate for CO2 sequestration from flue gas as well as for the production of value added substances. Copyright © 2013 Elsevier Ltd. All rights reserved.

Simplified models of transport and reactions in conditions of CO2 storage in saline aquifers

Science.gov (United States)

Suchodolska, Katarzyna; Labus, Krzysztof

2016-04-01

Simple hydrogeochemical models may serve as tools of preliminary assessment of CO2 injection and sequestraton impact on the aquifer and cap-rocks. In order to create models of reaction and transport in conditions of CO2 injection and storage, the TOUGHREACT simulator, and the Geochemist's Workbench software were applied. The chemical composition of waters for kinetic transport models based on the water - rock equilibrium calculations. Analyses of reaction and transport of substances during CO2 injection and storage period were carried out in three scenarios: one-dimensional radial model, and two-dimensional model of CO2 injection and sequestration, and one-dimensional model of aquifer - cap-rock interface. Modeling was performed in two stages. The first one simulated the immediate changes in the aquifer and insulating rocks impacted by CO2 injection (100 days in case of reaction model and 30 years in transport and reaction model), the second - enabled assessment of long-term effects of sequestration (20000 years). Reactions' quality and progress were monitored and their effects on formation porosity and sequestration capacity in form of mineral, residual and free phase of CO2 were calculated. Calibration of numerical models (including precipitation of secondary minerals, and correction of kinetics parameters) describing the initial stage of injection, was based on the experimental results. Modeling allowed to evaluate the pore space saturation with gas, changes in the composition and pH of pore waters, relationships between porosity and permeability changes and crystallization or dissolution minerals. We assessed the temporal and spatial extent of crystallization processes, and the amount of carbonates trapping. CO2 in mineral form. The calculated sequestration capacity of analyzed formations reached n·100 kg/m3 for the: dissolved phase - CO(aq), gas phase - CO2(g) and mineral phase, but as much as 101 kg/m3 for the supercritical phase - SCCO2. Processes of gas

Chloride cells as an index of the impacts of CO{sub 2} ocean sequestration on marine fish

Energy Technology Data Exchange (ETDEWEB)

Hayashi, M.; Ishimatsu, A. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.; Kikkawa, T. [Nagasaki Univ., Nagasaki (Japan). Marine Research Inst.]|[Marine Ecology Research Inst., Onjuku, Chiba (Japan). Central Laboratory

2005-07-01

Carbon dioxide (CO{sub 2}) ocean sequestration has been proposed as a potential measure to mitigate greenhouse gas emissions to the atmosphere. However, the impacts of CO{sub 2} ocean sequestration on marine organisms must be examined in discussing the feasibility of this mitigation measure. This study examined the changes in the morphology of chloride cells (CCs) and activity of Na{sup +}, K{sup +} -ATPase of the Japanese flounder Paralichthys olivaceus during aquatic hypercapnia. The apical openings area increased 1.3 and 4.1 times in 24 hour exposures to 1 per cent and 5 per cent CO{sub 2}, respectively, while the CCs area or density did not change at both concentrations. Gill Na{sup +}, K{sup +} -ATPase activity more than doubled at 72 hours and then decreased at 1 per cent CO{sub 2}, whereas it increased to 170 per cent at 24 hours during exposure to 5 per cent CO{sub 2} . These results suggest that branchial CCs are involved in acid-base regulation in marine fish under environmental hypercapnia. 4 refs., 2 figs.

Carbonation of steel slag for CO2 sequestration: Leaching of products and reaction mechanisms

NARCIS (Netherlands)

Huijgen, W.J.J.; Comans, R.N.J.

2006-01-01

Carbonation of industrial alkaline residues can be used as a CO2 sequestration technology to reduce carbon dioxide emissions. In this study, steel slag samples were carbonated to a varying extent. Leaching experiments and geochemical modeling were used to identify solubility-controlling processes of

Modeling of fate and transport of co-injection of H2S with CO2 in deep saline formations

Energy Technology Data Exchange (ETDEWEB)

Zhang, W.; Xu, T.; Li, Y.

2010-12-15

The geological storage of CO{sub 2} in deep saline formations is increasing seen as a viable strategy to reduce the release of greenhouse gases into the atmosphere. However, costs of capture and compression of CO{sub 2} from industrial waste streams containing small quantities of sulfur and nitrogen compounds such as SO{sub 2}, H{sub 2}S and N{sub 2} are very expensive. Therefore, studies on the co-injection of CO{sub 2} containing other acid gases from industrial emissions are very important. In this paper, numerical simulations were performed to study the co-injection of H{sub 2}S with CO{sub 2} in sandstone and carbonate formations. Results indicate that the preferential dissolution of H{sub 2}S gas (compared with CO{sub 2} gas) into formation water results in the delayed breakthrough of H{sub 2}S gas. Co-injection of H{sub 2}S results in the precipitation of pyrite through interactions between the dissolved H{sub 2}S and Fe{sup 2+} from the dissolution of Fe-bearing minerals. Additional injection of H{sub 2}S reduces the capabilities for solubility and mineral trappings of CO{sub 2} compared to the CO{sub 2} only case. In comparison to the sandstone (siliciclastic) formation, the carbonate formation is less favorable to the mineral sequestration of CO{sub 2}. Different from CO{sub 2} mineral trapping, the presence of Fe-bearing siliciclastic and/or carbonate is more favorable to the H{sub 2}S mineral trapping.

Gas geochemistry of natural analogues for the studies of geological CO2 sequestration

International Nuclear Information System (INIS)

Voltattorni, N.; Sciarra, A.; Caramanna, G.; Cinti, D.; Pizzino, L.; Quattrocchi, F.

2009-01-01

Geological sequestration of anthropogenic CO 2 appears to be a promising method for reducing the amount of greenhouse gases released to the atmosphere. Geochemical modelling of the storage capacity for CO 2 in saline aquifers, sandstones and/or carbonates should be based on natural analogues both in situ and in the laboratory. The main focus of this paper has been to study natural gas emissions representing extremely attractive surrogates for the study and prediction of the possible consequences of leakage from geological sequestration sites of anthropogenic CO 2 (i.e., the return to surface, potentially causing localised environmental problems). These include a comparison among three different Italian case histories: (i) the Solfatara crater (Phlegraean Fields caldera, southern Italy) is an ancient Roman spa. The area is characterised by intense and diffuse hydrothermal activity, testified by hot acidic mud pools, thermal springs and a large fumarolic field. Soil gas flux measurements show that the entire area discharges between 1200 and 1500 tons of CO 2 per day; (ii) the Panarea Island (Aeolian Islands, southern Italy) where a huge submarine volcanic-hydrothermal gas burst occurred in November, 2002. The submarine gas emissions chemically modified seawater causing a strong modification of the marine ecosystem. All of the collected gases are CO 2 -dominant (maximum value: 98.43 vol.%); (iii) the Tor Caldara area (Central Italy), located in a peripheral sector of the quiescent Alban Hills volcano, along the faults of the Ardea Basin transfer structure. The area is characterised by huge CO 2 degassing both from water and soil. Although the above mentioned areas do not represent a storage scenario, these sites do provide many opportunities to study near-surface processes and to test monitoring methodologies.

Chrysotile dissolution rates: Implications for carbon sequestration

International Nuclear Information System (INIS)

Thom, James G.M.; Dipple, Gregory M.; Power, Ian M.; Harrison, Anna L.

2013-01-01

Highlights: • Uncertainties in serpentine dissolution kinetics hinder carbon sequestration models. • A pH dependent, far from equilibrium dissolution rate law for chrysotile. • F chrysotile (mol/m 2 /s) = 10 −0.21pH−10.57 at 22 °C over pH 2–10. • Laboratory dissolution rates consistent with mine waste weathering observations. • Potential for carbon sequestration in mine tailings and aquifers is assessed. - Abstract: Serpentine minerals (e.g., chrysotile) are a potentially important medium for sequestration of CO 2 via carbonation reactions. The goals of this study are to report a steady-state, far from equilibrium chrysotile dissolution rate law and to better define what role serpentine dissolution kinetics will have in constraining rates of carbon sequestration via serpentine carbonation. The steady-state dissolution rate of chrysotile in 0.1 m NaCl solutions was measured at 22 °C and pH ranging from 2 to 8. Dissolution experiments were performed in a continuously stirred flow-through reactor with the input solutions pre-equilibrated with atmospheric CO 2 . Both Mg and Si steady-state fluxes from the chrysotile surface, and the overall chrysotile flux were regressed and the following empirical relationships were obtained: F Mg =-0.22pH-10.02;F Si =-0.19pH-10.37;F chrysotile =-0.21pH-10.57 where F Mg , F Si , and F chrysotile are the log 10 Mg, Si, and molar chrysotile fluxes in mol/m 2 /s, respectively. Element fluxes were used in reaction-path calculations to constrain the rate of CO 2 sequestration in two geological environments that have been proposed as potential sinks for anthropogenic CO 2 . Carbon sequestration in chrysotile tailings at 10 °C is approximately an order of magnitude faster than carbon sequestration in a serpentinite-hosted aquifer at 60 °C on a per kilogram of water basis. A serpentinite-hosted aquifer, however, provides a larger sequestration capacity. The chrysotile dissolution rate law determined in this study has

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.

Molecular simulations of CO2 at interfaces

DEFF Research Database (Denmark)

Silvestri, Alessandro

trapping mechanisms that act over dierent time scales, where eectiveness is determined by phenomena that occur at the interfaces between CO2, pore uids and the pore surfaces. Solid theoretical understanding of the nanoscale interactions that result from the interplay of intermolecular and surface forces...... variety of conditions: pressure, temperature, pore solution salinity and various mineral surfaces. However, achieving representative subsurface conditions in experiments is challenging and reported data are aected by experimental uncertainties and sometimes are contradictory. Molecular modelling...... rock record and the formations are generally porous so their probable response to CO2 sequestration needs to be investigated. However, despite the large number of geologic sequestration publications on water{rock interactions over the last decade, studies on carbonate reservoirs remain scarce...

An experimental study on mineral sequestration of CO{sub 2} in basics and ultra basics rocks; Etude experimentale des reactions de carbonatation minerale du CO{sub 2} dans les roches basiques et ultrabasiques

Energy Technology Data Exchange (ETDEWEB)

Dufaud, F

2006-11-15

The first part of the thesis is dedicated to dissolution data of siderite FeCO{sub 3} and magnetite Fe{sub 3}O{sub 4} which have been monitored in situ on the FAME beamline of the european synchrotron radiation facility in Grenoble. Iron in solution close to siderite single crystals is shown to be divalent hydrated. The small size of the experimentally investigated volume of solution (200 *400 micrometer and 3 mm height) allowed to work with single crystals in well defined geometries. No specific interaction was observed between iron (II) and dissolved inorganic carbon, suggesting that modelling siderite evolution under high CO{sub 2} pressures by using CO{sub 2}-less very acidic (pH 1-2) solutions is adequate. Using initial reaction rates, we get an activation energy for siderite dissolution of 62 kJ.mol{sup -1}, consistent with existing literature data. Such a value is suggestive of a mineral/solution interface mechanism.. Data from this study and from literature are consistent over a temperature range 25 C - 125 C and a pH range pH 1-7 with an empirical law: pk = pH + E{sub a}/(ln(10)*RT(K)) - log(S/V) - 10,5 where E{sub a} = 62 kJ.mol{sup -1} and S/V is the ratio between solid surface S and fluid volume V. A value of activation energy of 73.5 kJ.mol{sup -1} is obtained in the case of magnetite, also consistent with mineral/solution processes. The second and major part of the thesis work is the realization of analogical experiments for simulating carbonation of basic and ultra basic minerals. Experiments were carried out on consolidated rock cores at 90 C and 280 bar of CO{sub 2} (low temperature experiments) and on powders contained in metallic capsules at 400-500 C and 1000-1700 bars of CO{sub 2} (high temperature experiments). The rate of mineral storage of CO{sub 2} was defined as the molar ratio of solid carbonate formed over total CO{sub 2} injected. It is of about 1% in three months in low temperature experiments whereas it reaches several tens of

Rapid solubility and mineral storage of CO₂ in basalt

DEFF Research Database (Denmark)

Gislason, Sigurdur R.; Broecker, W.S.; Gunnlaugsson, E.

2014-01-01

The long-term security of geologic carbon storage is critical to its success and public acceptance. Much of the security risk associated with geological carbon storage stems from its buoyancy. Gaseous and supercritical CO2 are less dense than formation waters, providing a driving force for it to ......The long-term security of geologic carbon storage is critical to its success and public acceptance. Much of the security risk associated with geological carbon storage stems from its buoyancy. Gaseous and supercritical CO2 are less dense than formation waters, providing a driving force...... for it to escape back to the surface. This buoyancy can be eliminated by the dissolution of CO2 into water prior to, or during its injection into the subsurface. The dissolution makes it possible to inject into fractured rocks and further enhance mineral storage of CO2 especially if injected into silicate rocks...... rich in divalent metal cations such as basalts and ultra-mafic rocks. We have demonstrated the dissolution of CO2 into water during its injection into basalt leading to its geologic solubility storage in less than five minutes and potential geologic mineral storage within few years after injection [1...

Surface monitoring of microseismicity at the Decatur, Illinois, CO2 sequestration demonstration site

Science.gov (United States)

Kaven, Joern; Hickman, Stephen H.; McGarr, Arthur F.; Ellsworth, William L.

2015-01-01

Sequestration of CO2 into subsurface reservoirs can play an important role in limiting future emission of CO2 into the atmosphere (e.g., Benson and Cole, 2008). For geologic sequestration to become a viable option to reduce greenhouse gas emissions, large-volume injection of supercritical CO2 into deep sedimentary formations is required. These formations offer large pore volumes and good pore connectivity and are abundant (Bachu, 2003; U.S. Geological Survey Geologic Carbon Dioxide Storage Resources Assessment Team, 2013). However, hazards associated with injection of CO2 into deep formations require evaluation before widespread sequestration can be adopted safely (Zoback and Gorelick, 2012). One of these hazards is the potential to induce seismicity on pre-existing faults or fractures. If these faults or fractures are large and critically stressed, seismic events can occur with magnitudes large enough to pose a hazard to surface installations and, possibly more critical, the seal integrity of the cap rock. The Decatur, Illinois, carbon capture and storage (CCS) demonstration site is the first, and to date, only CCS project in the United States that injects a large volume of supercritical CO2 into a regionally extensive, undisturbed saline formation. The first phase of the Decatur CCS project was completed in November 2014 after injecting a million metric tons of supercritical CO2 over three years. This phase was led by the Illinois State Geological Survey (ISGS) and included seismic monitoring using deep borehole sensors, with a few sensors installed within the injection horizon. Although the deep borehole network provides a more comprehensive seismic catalog than is presented in this paper, these deep data are not publically available. We contend that for monitoring induced microseismicity as a possible seismic hazard and to elucidate the general patterns of microseismicity, the U.S. Geological Survey (USGS) surface and shallow borehole network described below

CO₂ Storage and Enhanced Oil Recovery: Bald Unit Test Site, Mumford Hills Oil Field, Posey County, Indiana

Energy Technology Data Exchange (ETDEWEB)

Frailey, Scott M. [Illinois State Geological Survey, Champaign, IL (United States); Krapac, Ivan G. [Illinois State Geological Survey, Champaign, IL (United States); Damico, James R. [Illinois State Geological Survey, Champaign, IL (United States); Okwen, Roland T. [Illinois State Geological Survey, Champaign, IL (United States); McKaskle, Ray W. [Illinois State Geological Survey, Champaign, IL (United States)

2012-03-30

The Midwest Geological Sequestration Consortium (MGSC) carried out a small-scale carbon dioxide (CO₂) injection test in a sandstone within the Clore Formation (Mississippian System, Chesterian Series) in order to gauge the large-scale CO₂ storage that might be realized from enhanced oil recovery (EOR) of mature Illinois Basin oil fields via miscible liquid CO₂ flooding.

Anthropogenic nitrogen deposition enhances carbon sequestration in boreal soils.

Science.gov (United States)

Maaroufi, Nadia I; Nordin, Annika; Hasselquist, Niles J; Bach, Lisbet H; Palmqvist, Kristin; Gundale, Michael J

2015-08-01

It is proposed that carbon (C) sequestration in response to reactive nitrogen (Nr ) deposition in boreal forests accounts for a large portion of the terrestrial sink for anthropogenic CO2 emissions. While studies have helped clarify the magnitude by which Nr deposition enhances C sequestration by forest vegetation, there remains a paucity of long-term experimental studies evaluating how soil C pools respond. We conducted a long-term experiment, maintained since 1996, consisting of three N addition levels (0, 12.5, and 50 kg N ha(-1) yr(-1) ) in the boreal zone of northern Sweden to understand how atmospheric Nr deposition affects soil C accumulation, soil microbial communities, and soil respiration. We hypothesized that soil C sequestration will increase, and soil microbial biomass and soil respiration will decrease, with disproportionately large changes expected compared to low levels of N addition. Our data showed that the low N addition treatment caused a non-significant increase in the organic horizon C pool of ~15% and a significant increase of ~30% in response to the high N treatment relative to the control. The relationship between C sequestration and N addition in the organic horizon was linear, with a slope of 10 kg C kg(-1) N. We also found a concomitant decrease in total microbial and fungal biomasses and a ~11% reduction in soil respiration in response to the high N treatment. Our data complement previous data from the same study system describing aboveground C sequestration, indicating a total ecosystem sequestration rate of 26 kg C kg(-1) N. These estimates are far lower than suggested by some previous modeling studies, and thus will help improve and validate current modeling efforts aimed at separating the effect of multiple global change factors on the C balance of the boreal region. © 2015 John Wiley & Sons Ltd.

Integrated Experimental and Modeling Studies of Mineral Carbonation as a Mechanism for Permanent Carbon Sequestration in Mafic/Ultramafic Rocks

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhengrong [Yale Univ., New Haven, CT (United States); Qiu, Lin [Yale Univ., New Haven, CT (United States); Zhang, Shuang [Yale Univ., New Haven, CT (United States); Bolton, Edward [Yale Univ., New Haven, CT (United States); Bercovici, David [Yale Univ., New Haven, CT (United States); Ague, Jay [Yale Univ., New Haven, CT (United States); Karato, Shun-Ichiro [Yale Univ., New Haven, CT (United States); Oristaglio, Michael [Yale Univ., New Haven, CT (United States); Zhu, Wen-Iu [Univ. of Maryland, College Park, MD (United States); Lisabeth, Harry [Univ. of Maryland, College Park, MD (United States); Johnson, Kevin [Univ. of Hawaii, Honolulu, HI (United States)

2014-09-30

) saturated with CO₂ brines of varying compositions. A goal of these geomechanical experiments was to see if flow and deformation processes, which accompany natural carbonation reactions in underground settings, work to enhance or inhibit the reactions. The experiments involved hydrostatic compaction, followed by deformation at a constant rate of strain. Sample permeability was monitored during the reactions. Comparison of the samples’ volume changes to their axial strains (shortening) during deformation indicates that samples reacted with CO₂-saturated brines accommodate more axial compaction, before the onset of dilation (a swelling that precedes rock failure), than samples reacted with distilled water. Analyses of the reacted samples with scanning electron microscope (SEM) images indicate, first, that dissolution of olivine occurring in the initial stages of carbonation can provide pathways to fluid flow that sustain the reaction, and, second, that carbonate minerals precipitated along existing fractures in the rocks may serve as asperities, or roughness on a crack’s surface that restricts its closure. Final Scientific/Technical Report DE-FE0004275 | Mineral Carbonation | 5 In a related study undertaken by one of the principal investigators as a spin-off of the main project, a simple model of (magnesite) crystal growth in the pore space of basalts undergoing carbonation was developed. The model suggests that, under a carefully controlled program of CO₂ injection, carbonate mineral growth can harden the rock formation against earthquakes that might otherwise be induced by the injection of large fluid volumes (Yarushina and Bercovici, 2013). The overall conclusion of the research project is that mineral carbonation of underground mafic and ultramafic rock formations is a viable candidate for long-term sequestration of man-made carbon dioxide. No results obtained during the project indicate that the method is inherently intractable in its

Enhanced Performance Assessment System (EPAS) for carbon sequestration.

Energy Technology Data Exchange (ETDEWEB)

Wang, Yifeng; Sun, Amy Cha-Tien; McNeish, Jerry A. (Sandia National Laboratories, Livermore, CA); Dewers, Thomas A.; Hadgu, Teklu; Jove-Colon, Carlos F.

2010-09-01

Carbon capture and sequestration (CCS) is an option to mitigate impacts of atmospheric carbon emission. Numerous factors are important in determining the overall effectiveness of long-term geologic storage of carbon, including leakage rates, volume of storage available, and system costs. Recent efforts have been made to apply an existing probabilistic performance assessment (PA) methodology developed for deep nuclear waste geologic repositories to evaluate the effectiveness of subsurface carbon storage (Viswanathan et al., 2008; Stauffer et al., 2009). However, to address the most pressing management, regulatory, and scientific concerns with subsurface carbon storage (CS), the existing PA methodology and tools must be enhanced and upgraded. For example, in the evaluation of a nuclear waste repository, a PA model is essentially a forward model that samples input parameters and runs multiple realizations to estimate future consequences and determine important parameters driving the system performance. In the CS evaluation, however, a PA model must be able to run both forward and inverse calculations to support optimization of CO{sub 2} injection and real-time site monitoring as an integral part of the system design and operation. The monitoring data must be continually fused into the PA model through model inversion and parameter estimation. Model calculations will in turn guide the design of optimal monitoring and carbon-injection strategies (e.g., in terms of monitoring techniques, locations, and time intervals). Under the support of Laboratory-Directed Research & Development (LDRD), a late-start LDRD project was initiated in June of Fiscal Year 2010 to explore the concept of an enhanced performance assessment system (EPAS) for carbon sequestration and storage. In spite of the tight time constraints, significant progress has been made on the project: (1) Following the general PA methodology, a preliminary Feature, Event, and Process (FEP) analysis was performed for

Reactor design considerations in mineral sequestration of carbon dioxide

International Nuclear Information System (INIS)

Ityokumbul, M.T.; Chander, S.; O'Connor, William K.; Dahlin, David C.; Gerdemann, Stephen J.

2001-01-01

One of the promising approaches to lowering the anthropogenic carbon dioxide levels in the atmosphere is mineral sequestration. In this approach, the carbon dioxide reacts with alkaline earth containing silicate minerals forming magnesium and/or calcium carbonates. Mineral carbonation is a multiphase reaction process involving gas, liquid and solid phases. The effective design and scale-up of the slurry reactor for mineral carbonation will require careful delineation of the rate determining step and how it changes with the scale of the reactor. The shrinking core model was used to describe the mineral carbonation reaction. Analysis of laboratory data indicates that the transformations of olivine and serpentine are controlled by chemical reaction and diffusion through an ash layer respectively. Rate parameters for olivine and serpentine carbonation are estimated from the laboratory data

ENGINEERING FEASIBILITY AND ECONOMICS OF CO2 SEQUESTRATION/USE ON AN EXISTING COAL-FIRED POWER PLANT: A LITERATURE REVIEW

Energy Technology Data Exchange (ETDEWEB)

Carl R. Bozzuto; Nsakala ya Nsakala

2000-01-31

The overall objective of this study is to evaluate the technical feasibility and the economics of alternate CO{sub 2} capture and sequestration/use technologies for retrofitting an existing pulverized coal-fired power plant. To accomplish this objective three alternative CO{sub 2} capture and sequestration systems will be evaluated to identify their impact on an existing boiler, associated boiler auxiliary components, overall plant operation and performance and power plant cost, including the cost of electricity. The three retrofit technologies that will be evaluated are as follows: (1) Coal combustion in air, followed by CO{sub 2} separation from flue gas with Kerr-McGee/ABB Lummus Global's commercial MEA-based absorption/stripping process. (2) Coal combustion in an O{sub 2}/CO{sub 2} environment with CO{sub 2} recycle. (3) Coal combustion in air with oxygen removal and CO{sub 2} captured by tertiary amines In support of this objective and execution of the evaluation of the three retrofit technologies a literature survey was conducted. It is presented in an ''annotated'' form, consistent with the following five sections: (1) Coal Combustion in O{sub 2}/CO{sub 2} Media; (2) Oxygen Separation Technologies; (3) Post Combustion CO{sub 2} Separation Technologies; (4) Potential Utilization of CO{sub 2}; and (5) CO{sub 2} Sequestration. The objective of the literature search was to determine if the three retrofit technologies proposed for this project continue to be sound choices. Additionally, a review of the literature would afford the opportunity to determine if other researchers have made significant progress in developing similar process technologies and, in that context, to revisit the current state-of-the-art. Results from this literature survey are summarized in the report.

CO{sub 2} solubility in brines of sedimentary basins. Application to CO{sub 2} sequestration (greenhouse gas); Solubilite de CO{sub 2} dans les saumures des bassins sedimentaires. Application au stockage de CO{sub 2} (gaz a effet de serre)

Energy Technology Data Exchange (ETDEWEB)

Portier, S.

2005-04-01

Large scale combustion of fossil energy leads today to a production of 20 billions tons of CO{sub 2} annually. This increases continuously the CO{sub 2} concentration in the atmosphere, responsible of the observed climatic increase of the temperature since one century. One of the most acceptable solutions consists in the so called CO{sub 2} sequestration in natural geological formations. The control of the process and the prediction of the final quantity of CO{sub 2} trapped in the deep saline aquifers depend on the knowledge of the solubility of acid gas in natural brines in the in situ temperature and pressure conditions. The possible dissolution of acid gases in aqueous phases brings a new complexity, owing to the fact that they behave like electrolytes in aqueous mediums A thermodynamic model for CO{sub 2} solubility is presented. The vapour phase is described by a cubic state equation. The aqueous phase is described by apparent constants of CO{sub 2} dissolution and dissociation, adjusted on literature data. This model is validated by measurements of the British Geological Survey (CO{sub 2} sequestration at Sleipner oil field, North Sea). The results of this study made it possible to calculate the impact of a CO{sub 2} injection on the solubility of calcite by acidification of formation water. The consequences in terms of CO{sub 2} storage capacity of deep saline aquifers are estimated. (author)

Soil fertility limits carbon sequestration by forest ecosystems in a CO2-enriched atmosphere

Science.gov (United States)

Ram Oren; David S. Ellsworth; Kurt H. Johnsen; Nathan Phillips; Brent E. Ewers; Chris Maier; Karina V.R. Schafer; Heather McCarthy; George Hendrey; Steven G. McNulty; Gabriel G. Katul

2001-01-01

Northern mid-latitude forests are a large terrestrial carbon sink. Ignoring nutrient limitations, large increases in carbon sequestration from carbon dioxide (CO2) fertilization are expected in these forests. Yet, forests are usually relegated to sites of moderate to poor fertility, where tree growth is often limited by nutrient supply, in...

Geologic Carbon Sequestration: Mitigating Climate Change by Injecting CO2 Underground (LBNL Summer Lecture Series)

Energy Technology Data Exchange (ETDEWEB)

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

2009-07-21

Summer Lecture Series 2009: Climate change provides strong motivation to reduce CO2 emissions from the burning of fossil fuels. Carbon dioxide capture and storage involves the capture, compression, and transport of CO2 to geologically favorable areas, where its injected into porous rock more than one kilometer underground for permanent storage. Oldenburg, who heads Berkeley Labs Geologic Carbon Sequestration Program, will focus on the challenges, opportunities, and research needs of this innovative technology.

A Full-Featured User Friendly CO₂-EOR and Sequestration Planning Software

Energy Technology Data Exchange (ETDEWEB)

Savage, Bill [Nitec LLC, Denver, CO (United States)

2013-11-30

A Full-Featured, User Friendly CO₂-EOR and Sequestration Planning Software This project addressed the development of an integrated software solution that includes a graphical user interface, numerical simulation, visualization tools and optimization processes for reservoir simulation modeling of CO₂-EOR. The objective was to assist the industry in the development of domestic energy resources by expanding the application of CO₂-EOR technologies, and ultimately to maximize the CO₂} sequestration capacity of the U.S. The software resulted in a field-ready application for the industry to address the current CO₂-EOR technologies. The software has been made available to the public without restrictions and with user friendly operating documentation and tutorials. The software (executable only) can be downloaded from NITEC’s website at www.nitecllc.com. This integrated solution enables the design, optimization and operation of CO₂-EOR processes for small and mid-sized operators, who currently cannot afford the expensive, time intensive solutions that the major oil companies enjoy. Based on one estimate, small oil fields comprise 30% of the of total economic resource potential for the application of CO₂-EOR processes in the U.S. This corresponds to 21.7 billion barrels of incremental, technically recoverable oil using the current “best practices”, and 31.9 billion barrels using “next-generation” CO₂-EOR techniques. The project included a Case Study of a prospective CO₂-EOR candidate field in Wyoming by a small independent, Linc Energy Petroleum Wyoming, Inc. NITEC LLC has an established track record of developing innovative and user friendly software. The Principle Investigator is an experienced manager and engineer with expertise in software development, numerical techniques, and GUI applications. Unique, presently-proprietary NITEC technologies have been integrated

Water Contact Angle Dependence with Hydroxyl Functional Groups on Silica Surfaces under CO2 Sequestration Conditions.

Science.gov (United States)

Chen, Cong; Zhang, Ning; Li, Weizhong; Song, Yongchen

2015-12-15

Functional groups on silica surfaces under CO2 sequestration conditions are complex due to reactions among supercritical CO2, brine and silica. Molecular dynamics simulations have been performed to investigate the effects of hydroxyl functional groups on wettability. It has been found that wettability shows a strong dependence on functional groups on silica surfaces: silanol number density, space distribution, and deprotonation/protonation degree. For neutral silica surfaces with crystalline structure (Q(3), Q(3)/Q(4), Q(4)), as silanol number density decreases, contact angle increases from 33.5° to 146.7° at 10.5 MPa and 318 K. When Q(3) surface changes to an amorphous structure, water contact angle increases 20°. Water contact angle decreases about 12° when 9% of silanol groups on Q(3) surface are deprotonated. When the deprotonation degree increases to 50%, water contact angle decreases to 0. The dependence of wettability on silica surface functional groups was used to analyze contact angle measurement ambiguity in literature. The composition of silica surfaces is complicated under CO2 sequestration conditions, the results found in this study may help to better understand wettability of CO2/brine/silica system.

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.

Velocity Model for CO2 Sequestration in the Southeastern United States Atlantic Continental Margin

Science.gov (United States)

Ollmann, J.; Knapp, C. C.; Almutairi, K.; Almayahi, D.; Knapp, J. H.

2017-12-01

The sequestration of carbon dioxide (CO2) is emerging as a major player in offsetting anthropogenic greenhouse gas emissions. With 40% of the United States' anthropogenic CO2 emissions originating in the southeast, characterizing potential CO2 sequestration sites is vital to reducing the United States' emissions. The goal of this research project, funded by the Department of Energy (DOE), is to estimate the CO2 storage potential for the Southeastern United States Atlantic Continental Margin. Previous studies find storage potential in the Atlantic continental margin. Up to 16 Gt and 175 Gt of storage potential are estimated for the Upper Cretaceous and Lower Cretaceous formations, respectively. Considering 2.12 Mt of CO2 are emitted per year by the United States, substantial storage potential is present in the Southeastern United States Atlantic Continental Margin. In order to produce a time-depth relationship, a velocity model must be constructed. This velocity model is created using previously collected seismic reflection, refraction, and well data in the study area. Seismic reflection horizons were extrapolated using well log data from the COST GE-1 well. An interpolated seismic section was created using these seismic horizons. A velocity model will be made using P-wave velocities from seismic reflection data. Once the time-depth conversion is complete, the depths of stratigraphic units in the seismic refraction data will be compared to the newly assigned depths of the seismic horizons. With a lack of well control in the study area, the addition of stratigraphic unit depths from 171 seismic refraction recording stations provides adequate data to tie to the depths of picked seismic horizons. Using this velocity model, the seismic reflection data can be presented in depth in order to estimate the thickness and storage potential of CO2 reservoirs in the Southeastern United States Atlantic Continental Margin.

System analysis of CO_2 sequestration from biomass cogeneration plants (Bio-CHP-CCS). Technology, economic efficiency, sustainability

International Nuclear Information System (INIS)

Hartmann, Claus

2014-10-01

In the present work a system analysis is carried out to determine the extent to which a combination of the three areas of energetic biomass use, combined heat and power (CHP) and CO_2 sequestration (CCS - Carbon Capture and Storage) is fundamentally possible and meaningful. The term ''CO_2 sequestration'' refers to the process chain from CO_2 capture, CO_2 transport and CO_2 storage. While the use of biomass in combined heat and power plants is a common practice, CO_2 sequestration (based on fossil fuels) is at the research and development stage. A combination of CCS with biomass has so far been little studied, a combination with combined heat and power plants has not been investigated at all. The two technologies for the energetic use of biomass and cogeneration represent fixed variables in the energy system of the future in the planning of the German federal government. According to the lead scenario of the Federal Ministry of the Environment, electricity generation from biomass is to be almost doubled from 2008 to 2020. At the same time, the heat generated in cogeneration is to be trebled [cf. Nitsch and Wenzel, 2009, p. 10]. At the same time, the CCS technology is to be used in half of all German coal-fired power plants until 2030 [cf. Krassuki et al., 2009, p. 17]. The combination of biomass and CCS also represents an option which is conceivable for the German federal policy [cf. Bundestag, 2008b, p. 4]. In addition, the CCS technology will provide very good export opportunities for the German economy in the future [cf. Federal Government, 2010, p. 20]. The combination of biomass combined heat and power plants with CCS offers the interesting opportunity to actively remove CO_2 from the atmosphere as a future climate protection instrument by means of CO_2 neutrality. Therefore, in the energy concept of the German federal government called for a storage project for industrial or biogenic CO_2 emissions to be established until 2020, as well as the use of CO_2 as

Mineral CO2 sequestration in basalts and ultra-basic rocks: impact of secondary silicated phases on the carbonation process

International Nuclear Information System (INIS)

Sissmann, Olivier

2013-01-01

The formation of carbonates constitutes a stable option for carbon dioxide (CO 2 ) geological sequestration, and is prone to play a significant role in reducing emissions of anthropic origin. However, our comprehension of the carbonation mechanism, as well as of the kinetics limitations encountered during this chemical reaction, remains poorly developed. Though there is a large number of studies focusing on the dissolution kinetics of basic silicates and on the precipitation of carbonates, few have inquired about the impact that the formation of non-carbonated secondary phases can have on these reaction's kinetics. It is the approach chosen here, as only solid knowledge of the global carbonation mechanism can make this process predictive and efficient. Experimental data on dissolution and carbonation have therefore been determined in batch reactors, on relevant minerals and rocks. Firstly, we studied the carbonation of olivine (a major phase within peridotites and minor within basalts) at 90 deg. C and under pCO 2 of 280 bars. The dissolution of San Carlos olivine (Mg 1.76 Fe 0.24 SiO 4 ) is slowed down by the formation of a surface silica gel, when the fluid reaches equilibrium with amorphous silica. The transport of species to the reactive medium becomes the limiting step of the process, slowing down the dissolution process of San Carlos olivine by 5 orders of magnitude. However, this passivation doesn't occur during the alteration of Ca-olivine (Ca 2 SiO 4 ), though a surface silica layer does form. This comparison suggests that it isn't the structure of the silicate but its chemical composition, which controls the transport properties through the interfacial layer. The second part explores the effects of organic ligands and of temperature variations on the formation of those phases. The addition of citrate at 90 deg. C increases the kinetics of San Carlos olivine by one order of magnitude, and allows the release of enough Mg in the aqueous medium to form

Scientific and Engineering Progress in CO2 Mineralization Using Industrial Waste and Natural Minerals

Directory of Open Access Journals (Sweden)

Heping Xie

2015-03-01

Full Text Available The issues of reducing CO2 levels in the atmosphere, sustainably utilizing natural mineral resources, and dealing with industrial waste offer challenging opportunities for sustainable development in energy and the environment. The latest advances in CO2 mineralization technology involving natural minerals and industrial waste are summarized in this paper, with great emphasis on the advancement of fundamental science, economic evaluation, and engineering applications. We discuss several leading large-scale CO2 mineralization methodologies from a technical and engineering-science perspective. For each technology option, we give an overview of the technical parameters, reaction pathway, reactivity, procedural scheme, and laboratorial and pilot devices. Furthermore, we present a discussion of each technology based on experimental results and the literature. Finally, current gaps in knowledge are identified in the conclusion, and an overview of the challenges and opportunities for future research in this field is provided.

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.

Gas geochemistry of natural analogues for the studies of geological CO{sub 2} sequestration

Energy Technology Data Exchange (ETDEWEB)

Voltattorni, N., E-mail: nunzia.voltattorni@ingv.it [Istituto Nazionale di Geofisica e Vulcanologia, Via di Vigna Murata no 605, 00143 Rome (Italy); Sciarra, A. [Istituto Nazionale di Geofisica e Vulcanologia, Via di Vigna Murata no 605, 00143 Rome (Italy); Caramanna, G. [Earth Science Dep., University ' La Sapienza' , Piazzale A. Moro no 5, 00185 Rome (Italy); Cinti, D.; Pizzino, L.; Quattrocchi, F. [Istituto Nazionale di Geofisica e Vulcanologia, Via di Vigna Murata no 605, 00143 Rome (Italy)

2009-07-15

Geological sequestration of anthropogenic CO{sub 2} appears to be a promising method for reducing the amount of greenhouse gases released to the atmosphere. Geochemical modelling of the storage capacity for CO{sub 2} in saline aquifers, sandstones and/or carbonates should be based on natural analogues both in situ and in the laboratory. The main focus of this paper has been to study natural gas emissions representing extremely attractive surrogates for the study and prediction of the possible consequences of leakage from geological sequestration sites of anthropogenic CO{sub 2} (i.e., the return to surface, potentially causing localised environmental problems). These include a comparison among three different Italian case histories: (i) the Solfatara crater (Phlegraean Fields caldera, southern Italy) is an ancient Roman spa. The area is characterised by intense and diffuse hydrothermal activity, testified by hot acidic mud pools, thermal springs and a large fumarolic field. Soil gas flux measurements show that the entire area discharges between 1200 and 1500 tons of CO{sub 2} per day; (ii) the Panarea Island (Aeolian Islands, southern Italy) where a huge submarine volcanic-hydrothermal gas burst occurred in November, 2002. The submarine gas emissions chemically modified seawater causing a strong modification of the marine ecosystem. All of the collected gases are CO{sub 2}-dominant (maximum value: 98.43 vol.%); (iii) the Tor Caldara area (Central Italy), located in a peripheral sector of the quiescent Alban Hills volcano, along the faults of the Ardea Basin transfer structure. The area is characterised by huge CO{sub 2} degassing both from water and soil. Although the above mentioned areas do not represent a storage scenario, these sites do provide many opportunities to study near-surface processes and to test monitoring methodologies.

Offshore Membrane Enclosures for Growing Algae (OMEGA: A System for Biofuel Production, Wastewater Treatment, and CO2 Sequestration

Science.gov (United States)

Trent, Jonathan; Embaye, Tsegereda; Buckwalter, Patrick; Richardson, Tra-My; Kagawa, Hiromi; Reinsch, Sigrid; Martis, Mary

2010-01-01

We are developing Offshore Membrane Enclosures for Growing Algae (OMEGA). OMEGAs are closed photo-bioreactors constructed of flexible, inexpensive, and durable plastic with small sections of semi-permeable membranes for gas exchange and forward osmosis (FO). Each OMEGA modules is filled with municipal wastewater and provided with CO2 from coastal CO2 sources. The OMEGA modules float just below the surface, and the surrounding seawater provides structural support, temperature control, and mixing for the freshwater algae cultures inside. The salinit7 gradient from inside to outside drives forward osmosis through the patches of FO membranes. This concentrates nutrients in the wastewater, which enhances algal growth, and slowly dewaters the algae, which facilitates harvesting. Thy concentrated algal biomass is harvested for producing biofuels and fertilizer. OMEGA system cleans the wastewater released into the surrounding coastal waters and functions as a carbon sequestration system.

Removal of Hg, As in FGD gypsum by different aqueous ammonia (amines) during CO2 sequestration.

Science.gov (United States)

Wenyi, Tan; Wenhui, Fan; Hongyi, Li; Zixin, Zhang; Yunkun, Zhu

2017-12-01

CO 2 sequestration by flue gas desulfurization gypsum (FGDG) has become a promising FGDG disposal technology due to simultaneous CO 2 emission reduction and FGDG conversion into calcium carbonate. In this paper, another merit of the novel technology, i.e., the removal of toxic elements (e.g., Hg and As) in FGDG, will be addressed for the first time. In three different aqueous ammonia (or amines) media, removal efficiencies of Hg and As in FGDG samples were evaluated during CO 2 sequestration. Higher than 90% and 20% removal efficiencies, respectively, for Hg and As are achieved at 40°C in aqueous ammonia media, but they decrease at elevated temperatures. Ammonia loss takes place at 80°C and pH varies greatly with temperatures in aqueous ammonia. This is disadvantageous for the formation of Hg-ammonia complexes and for the yield of carbonates, which are responsible for Hg or As re-adsorption. The sequential chemical extraction method suggests that the speciation changes of Hg are induced by FGDG carbonation, and that unstable Hg speciation in triethanolamine increases at elevated temperatures.

CO{sub 2} emissions: mineral carbonation and Finnish pulp and paper industry (CO{sub Nordic Plus}) and use of serpentinites in energy and metal industry (ECOSERP); Hiilidioksidipaeaestoet: Mineraalikarbonointi ja Suomen massaja paperiteollisuus (CO{sub 2} Nordic plus) ja serpentiinin hyoetykaeyttoe energia- ja metalliteollisuudessa (ECOSERP)

Energy Technology Data Exchange (ETDEWEB)

Fogelholm, C.J.; Raiski, T.; Teir, S. [Helsinki Univ. of Technology, Espoo (Finland). Lab of Energy Engineering and Environmental Protection

2006-12-19

Mineral carbonation has been investigated at Helsinki University of Technology (TKK), laboratory of energy engineering and environmental protection since year 2000. The Finnish Technology Agency Tekes and the Finnish Recovery Boiler Committee are funding through the ClimBus technology programme, in conjunction with the Nordic Energy Research Programme, the research regarding the application of ex situ mineral carbonation processes. One aspect is to verify the possible use of mineral carbonation for the separation, utilisation and long-term storage of carbon dioxide (CO2) in the pulp and paper industry. The Geological Survey of Finland (GTK) has been screening since 2004 the location, quality and suitability of the Finnish processed serpentine and stopped serpentinite storage of mines and in situ serpentinite bodies of ultramafic rock formations for mineral carbonation of CO2. Tekes and the GTK are funding development work through the ClimBus technology programme on the utilisation of serpentine and serpentinite for CO2 sequestration purposes, based on economical and environmental evaluation of mineral and mining processing operations. Also the options for other use of serpentine and serpentinite are evaluated. The most promising magnesium and calcium-based sources for carbonation are by products of mining processes of ultramafic rocks (such as serpentinites and serpentine) and steelmaking slags. Carbonated minerals could possibly be used as paper coating materials (PCC), fillers or construction materials. For magnesium carbonate new markets and applications must be developed. (orig.)

Performance evaluation of a green process for microalgal CO2 sequestration in closed photobioreactor using flue gas generated in-situ.

Science.gov (United States)

Yadav, Geetanjali; Karemore, Ankush; Dash, Sukanta Kumar; Sen, Ramkrishna

2015-09-01

In the present study, carbon-dioxide capture from in situ generated flue gas was carried out using Chlorella sp. in bubble column photobioreactors to develop a cost effective process for concomitant carbon sequestration and biomass production. Firstly, a comparative analysis of CO2 sequestration with varying concentrations of CO2 in air-CO2 and air-flue gas mixtures was performed. Chlorella sp. was found to be tolerant to 5% CO2 concentration. Subsequently, inhibitory effect of pure flue gas was minimized using various strategies like use of high initial cell density and photobioreactors in series. The final biofixation efficiency was improved by 54% using the adopted strategies. Further, sequestered microalgal biomass was analyzed for various biochemical constituents for their use in food, feed or biofuel applications. Copyright © 2015 Elsevier Ltd. All rights reserved.

Mineral Dissolution and Precipitation due to Carbon Dioxide-Water-Rock Interactions: The Significance of Accessory Minerals in Carbonate Reservoirs (Invited)

Science.gov (United States)

Kaszuba, J. P.; Marcon, V.; Chopping, C.

2013-12-01

Accessory minerals in carbonate reservoirs, and in the caprocks that seal these reservoirs, can provide insight into multiphase fluid (CO2 + H2O)-rock interactions and the behavior of CO2 that resides in these water-rock systems. Our program integrates field data, hydrothermal experiments, and geochemical modeling to evaluate CO2-water-rock reactions and processes in a variety of carbonate reservoirs in the Rocky Mountain region of the US. These studies provide insights into a wide range of geologic environments, including natural CO2 reservoirs, geologic carbon sequestration, engineered geothermal systems, enhanced oil and gas recovery, and unconventional hydrocarbon resources. One suite of experiments evaluates the Madison Limestone on the Moxa Arch, Southwest Wyoming, a sulfur-rich natural CO2 reservoir. Mineral textures and geochemical features developed in the experiments suggest that carbonate minerals which constitute the natural reservoir will initially dissolve in response to emplacement of CO2. Euhedral, bladed anhydrite concomitantly precipitates in response to injected CO2. Analogous anhydrite is observed in drill core, suggesting that secondary anhydrite in the natural reservoir may be related to emplacement of CO2 into the Madison Limestone. Carbonate minerals ultimately re-precipitate, and anhydrite dissolves, as the rock buffers the acidity and reasserts geochemical control. Another suite of experiments emulates injection of CO2 for enhanced oil recovery in the Desert Creek Limestone (Paradox Formation), Paradox Basin, Southeast Utah. Euhedral iron oxyhydroxides (hematite) precipitate at pH 4.5 to 5 and low Eh (approximately -0.1 V) as a consequence of water-rock reaction. Injection of CO2 decreases pH to approximately 3.5 and increases Eh by approximately 0.1 V, yielding secondary mineralization of euhedral pyrite instead of iron oxyhydroxides. Carbonate minerals also dissolve and ultimately re-precipitate, as determined by experiments in the

Interactions between the Design and Operation of Shale Gas Networks, Including CO2 Sequestration

Directory of Open Access Journals (Sweden)

Sharifzadeh Mahdi

2017-04-01

Full Text Available As the demand for energy continues to increase, shale gas, as an unconventional source of methane (CH4, shows great potential for commercialization. However, due to the ultra-low permeability of shale gas reservoirs, special procedures such as horizontal drilling, hydraulic fracturing, periodic well shut-in, and carbon dioxide (CO2 injection may be required in order to boost gas production, maximize economic benefits, and ensure safe and environmentally sound operation. Although intensive research is devoted to this emerging technology, many researchers have studied shale gas design and operational decisions only in isolation. In fact, these decisions are highly interactive and should be considered simultaneously. Therefore, the research question addressed in this study includes interactions between design and operational decisions. In this paper, we first establish a full-physics model for a shale gas reservoir. Next, we conduct a sensitivity analysis of important design and operational decisions such as well length, well arrangement, number of fractures, fracture distance, CO2 injection rate, and shut-in scheduling in order to gain in-depth insights into the complex behavior of shale gas networks. The results suggest that the case with the highest shale gas production may not necessarily be the most profitable design; and that drilling, fracturing, and CO2 injection have great impacts on the economic viability of this technology. In particular, due to the high costs, enhanced gas recovery (EGR using CO2 does not appear to be commercially competitive, unless tax abatements or subsidies are available for CO2 sequestration. It was also found that the interactions between design and operational decisions are significant and that these decisions should be optimized simultaneously.

CO2 emissions: mineral carbonation and Finnish pulp and paper industry (CONordicPlus) and use of serpentinites in energy and metal industry (ECOSERP)

International Nuclear Information System (INIS)

Fogelholm, C.J.; Raiski, T.; Teir, S.

2006-01-01

Mineral carbonation has been investigated at Helsinki University of Technology (TKK), laboratory of energy engineering and environmental protection since year 2000. The Finnish Technology Agency Tekes and the Finnish Recovery Boiler Committee are funding through the ClimBus technology programme, in conjunction with the Nordic Energy Research Programme, the research regarding the application of ex situ mineral carbonation processes. One aspect is to verify the possible use of mineral carbonation for the separation, utilisation and long-term storage of carbon dioxide (CO2) in the pulp and paper industry. The Geological Survey of Finland (GTK) has been screening since 2004 the location, quality and suitability of the Finnish processed serpentine and stopped serpentinite storage of mines and in situ serpentinite bodies of ultramafic rock formations for mineral carbonation of CO2. Tekes and the GTK are funding development work through the ClimBus technology programme on the utilisation of serpentine and serpentinite for CO2 sequestration purposes, based on economical and environmental evaluation of mineral and mining processing operations. Also the options for other use of serpentine and serpentinite are evaluated. The most promising magnesium and calcium-based sources for carbonation are by products of mining processes of ultramafic rocks (such as serpentinites and serpentine) and steelmaking slags. Carbonated minerals could possibly be used as paper coating materials (PCC), fillers or construction materials. For magnesium carbonate new markets and applications must be developed. (orig.)

ANALYSIS OF DEVONIAN BLACK SHALES IN KENTUCKY FOR POTENTIAL CARBON DIOXIDE SEQUESTRATION AND ENHANCED NATURAL GAS PRODUCTION

Energy Technology Data Exchange (ETDEWEB)

Brandon C. Nuttall

2003-07-28

CO{sub 2} emissions from the combustion of fossil fuels have been linked to global climate change. Proposed carbon management technologies include geologic sequestration of CO{sub 2}. A possible, but untested, sequestration strategy is to inject CO{sub 2} into organic-rich shales. Devonian black shales underlie approximately two-thirds of Kentucky and are thicker and deeper in the Illinois and Appalachian Basin portions of Kentucky than in central Kentucky. The Devonian black shales serve as both the source and trap for large quantities of natural gas; total gas in place for the shales in Kentucky is estimated to be between 63 and 112 trillion cubic feet. Most of this natural gas is adsorbed on clay and kerogen surfaces, analogous to methane storage in coal beds. In coals, it has been demonstrated that CO{sub 2} is preferentially adsorbed, displacing methane. Black shales may similarly desorb methane in the presence of CO{sub 2}. The concept that black, organic-rich Devonian shales could serve as a significant geologic sink for CO{sub 2} is the subject of current research. To accomplish this investigation, drill cuttings and cores were selected from the Kentucky Geological Survey Well Sample and Core Library. Methane and carbon dioxide adsorption analyses are being performed to determine the gas-storage potential of the shale and to identify shale facies with the most sequestration potential. In addition, sidewall core samples are being acquired to investigate specific black-shale facies, their potential CO{sub 2} uptake, and the resulting displacement of methane. Advanced logging techniques (elemental capture spectroscopy) are being investigated for possible correlations between adsorption capacity and geophysical log measurements. Initial estimates indicate a sequestration capacity of 5.3 billion tons CO{sub 2} in the Lower Huron Member of the Ohio shale in parts of eastern Kentucky and as much as 28 billion tons total in the deeper and thicker portions of the

Dissolution of cemented fractures in gas bearing shales in the context of CO2 sequestration

Science.gov (United States)

Kwiatkowski, Kamil; Szymczak, Piotr

2016-04-01

Carbon dioxide has a stronger binding than methane to the organic matter contained in the matrix of shale rocks [1]. Thus, the injection of CO2 into shale formation may enhance the production rate and total amount of produced methane, and simultaneously permanently store pumped CO2. Carbon dioxide can be injected during the initial fracking stage as CO2 based hydraulic fracturing, and/or later, as a part of enhanced gas recovery (EGR) [2]. Economic and environmental benefits makes CO2 sequestration in shales potentially very for industrial-scale operation [3]. However, the effective process requires large area of fracture-matrix interface, where CO2 and CH4 can be exchanged. Usually natural fractures, existing in shale formation, are preferentially reactivated during hydraulic fracturing, thus they considerably contribute to the flow paths in the resulting fracture system [4]. Unfortunately, very often these natural fractures are sealed by calcite [5]. Consequently the layer of calcite coating surfaces impedes exchange of gases, both CO2 and CH4, between shale matrix and fracture. In this communication we address the question whether carbonic acid, formed when CO2 is mixed with brine, is able to effectively dissolve a calcite layer present in the natural fractures. We investigate numerically fluid flow and dissolution of calcite coating in natural shale fractures, with CO2-brine mixture as a reactive fluid. Moreover, we discuss the differences between slow dissolution (driven by carbonic acid) and fast dissolution (driven by stronger hydrochloric acid) of calcite layer. We compare an impact of the flow rate and geometry of the fracture on the parameters of practical importance: available surface area, morphology of dissolution front, time scale of the dissolution, and the penetration length. We investigate whether the dissolution is sufficiently non-uniform to retain the fracture permeability, even in the absence of the proppant. The sizes of analysed fractures

Supercritical CO 2 -philic nanoparticles suitable for determining the viability of carbon sequestration in shale

KAUST Repository

Xu, Yisheng

2015-01-01

© The Royal Society of Chemistry. A fracture spacing less than a decimeter is probably required for the successful sequestration of CO2 in shale. Tracer experiments using inert nanoparticles could determine if a fracturing this intense has been achieved. Here we describe the synthesis of supercritical CO2-philic nanoparticles suitable for this application. The nanoparticles are ~50 nm in diameter and consist of iron oxide (Fe3O4) and silica (SiO2) cores functionalized with a fluorescent polymeric corona. The nanoparticles stably disperse in supercritical carbon dioxide (scCO2) and are detectable to concentrations of 10 ppm. This journal is

Allaying public concern regarding CO{sub 2} geological sequestration through the development of automated stations for the continuous geochemical monitoring of gases in the near surface environment

Energy Technology Data Exchange (ETDEWEB)

Annunziatellis, A.; Beaubien, S.E.; Ciotoli, G.; Lombardi, S. [La Sapienza Univ., Rome (Italy). Dept. of Earth Sciences

2005-07-01

Several carbon dioxide (CO{sub 2}) enhanced oil recovery projects conducted in North America have demonstrated that the deep, onshore geological sequestration of anthropogenic CO{sub 2} is technically feasible. However, the technology has yet to be proven to regulators and the general public. It must be demonstrated that carbon sequestration will result in the long-term isolation of the injected CO{sub 2} and that there is no health risk for local residents due to the leakage of CO{sub 2} at surface. It was suggested that in order to alleviate these concerns, low-cost, early warning systems should be installed to monitor gas compositions and concentrations in the soil gas and groundwater. Doing so, would trigger a warning if any increased concentrations of CO{sub 2} or other associated gases were noted in these phases, and allow for early examination of the cause of the anomalous value. In addition, since gas flow is typically along natural faults or abandoned bore holes, installation of monitoring stations around these higher risk sites would help maximize efficiency while minimizing costs. In this study, gas permeable tubing was used to sample soil gas or gases dissolved in groundwater via diffusion. In the case of equilibration with a gas phase the gas concentration within the tubing will eventually match that of the surrounding environment, whereas in the aqueous phase the internal volume of the tube will represent a head space where equilibrium concentrations will be governed by Henry's Constant. CO{sub 2}, hydrogen and hydrogen sulphide from either soil-gas or groundwater were analyzed with low cost infra-red electrochemical detectors. The data was processed with an integrated computer and the results were sent automatically via modem to a central laboratory. The prototype was installed in the San Vittorino Plain in central Italy where it has collected over 5 months of continuous CO{sub 2} data in an area susceptible to sinkhole formation caused by the

Application of Cutting-Edge 3D Seismic Attribute Technology to the Assessment of Geological Reservoirs for CO2 Sequestration

Energy Technology Data Exchange (ETDEWEB)

Christopher Liner; Jianjun Zeng; Po Geng Heather King Jintan Li; Jennifer Califf; John Seales

2010-03-31

The goals of this project were to develop innovative 3D seismic attribute technologies and workflows to assess the structural integrity and heterogeneity of subsurface reservoirs with potential for CO{sub 2} sequestration. Our specific objectives were to apply advanced seismic attributes to aide in quantifying reservoir properies and lateral continuity of CO{sub 2} sequestration targets. Our study area is the Dickman field in Ness County, Kansas, a type locality for the geology that will be encountered for CO{sub 2} sequestration projects from northern Oklahoma across the U.S. midcontent to Indiana and beyond. Since its discovery in 1962, the Dickman Field has produced about 1.7 million barrels of oil from porous Mississippian carbonates with a small structural closure at about 4400 ft drilling depth. Project data includes 3.3 square miles of 3D seismic data, 142 wells, with log, some core, and oil/water production data available. Only two wells penetrate the deep saline aquifer. Geological and seismic data were integrated to create a geological property model and a flow simulation grid. We systematically tested over a dozen seismic attributes, finding that curvature, SPICE, and ANT were particularly useful for mapping discontinuities in the data that likely indicated fracture trends. Our simulation results in the deep saline aquifer indicate two effective ways of reducing free CO{sub 2}: (a) injecting CO{sub 2} with brine water, and (b) horizontal well injection. A tuned combination of these methods can reduce the amount of free CO{sub 2} in the aquifer from over 50% to less than 10%.

Profitability Evaluation of a Hybrid Geothermal and CO2 Sequestration Project for a Coastal Hot Saline Aquifer.

Science.gov (United States)

Plaksina, Tatyana; Kanfar, Mohammed

2017-11-01

With growing interest in commercial projects involving industrial volume CO2 sequestration, a concern about proper containment and control over the gas plume becomes particularly prominent. In this study, we explore the potential of using a typical coastal geopressured hot saline aquifer for two commercial purposes. The first purpose is to harvest geothermal heat of the aquifer for electricity generation and/or direct use and the second one is to utilize the same rock volume for safe and controlled CO2 sequestration without interruption of heat production. To achieve these goals, we devised and economically evaluated a scheme that recovers operational and capital costs within first 4 years and yields positive internal rate of return of about 15% at the end of the operations. Using our strategic design of well placement and operational scheduling, we were able to achieve in our numerical simulation study the following results. First, the hot water production rates allowed to run a 30 MW organic Rankine cycle plant for 20 years. Second, during the last 10 years of operation we managed to inject into the same reservoir (volume of 0.8 x 109 m3) approximately 10 million ton of the supercritical gas. Third, decades of numerical monitoring the plume after the end of the operations showed that this large volume of CO2 is securely sequestrated inside the reservoir without compromising the caprock integrity.

Optimizing geologic CO2 sequestration by injection in deep saline formations below oil reservoirs

International Nuclear Information System (INIS)

Han, Weon Shik; McPherson, Brian J.

2009-01-01

The purpose of this research is to present a best-case paradigm for geologic CO 2 storage: CO 2 injection and sequestration in saline formations below oil reservoirs. This includes the saline-only section below the oil-water contact (OWC) in oil reservoirs, a storage target neglected in many current storage capacity assessments. This also includes saline aquifers (high porosity and permeability formations) immediately below oil-bearing formations. While this is a very specific injection target, we contend that most, if not all, oil-bearing basins in the US contain a great volume of such strata, and represent a rather large CO 2 storage capacity option. We hypothesize that these are the best storage targets in those basins. The purpose of this research is to evaluate this hypothesis. We quantitatively compared CO 2 behavior in oil reservoirs and brine formations by examining the thermophysical properties of CO 2 , CO 2 -brine, and CO 2 -oil in various pressure, temperature, and salinity conditions. In addition, we compared the distribution of gravity number (N), which characterizes a tendency towards buoyancy-driven CO 2 migration, and mobility ratio (M), which characterizes the impeded CO 2 migration, in oil reservoirs and brine formations. Our research suggests competing advantages and disadvantages of CO 2 injection in oil reservoirs vs. brine formations: (1) CO 2 solubility in oil is significantly greater than in brine (over 30 times); (2) the tendency of buoyancy-driven CO 2 migration is smaller in oil reservoirs because density contrast between oil and CO 2 is smaller than it between brine and oil (the approximate density contrast between CO 2 and crude oil is ∼100 kg/m 3 and between CO 2 and brine is ∼350 kg/m 3 ); (3) the increased density of oil and brine due to the CO 2 dissolution is not significant (about 7-15 kg/m 3 ); (4) the viscosity reduction of oil due to CO 2 dissolution is significant (from 5790 to 98 mPa s). We compared these competing

Mineral storage of CO2/H2S gas mixture injection in basaltic rocks