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Sample records for dioxide capture process

  1. Carbon dioxide capture process with regenerable sorbents

    DOEpatents

    Pennline, Henry W.; Hoffman, James S.

    2002-05-14

    A process to remove carbon dioxide from a gas stream using a cross-flow, or a moving-bed reactor. In the reactor the gas contacts an active material that is an alkali-metal compound, such as an alkali-metal carbonate, alkali-metal oxide, or alkali-metal hydroxide; or in the alternative, an alkaline-earth metal compound, such as an alkaline-earth metal carbonate, alkaline-earth metal oxide, or alkaline-earth metal hydroxide. The active material can be used by itself or supported on a substrate of carbon, alumina, silica, titania or aluminosilicate. When the active material is an alkali-metal compound, the carbon-dioxide reacts with the metal compound to generate bicarbonate. When the active material is an alkaline-earth metal, the carbon dioxide reacts with the metal compound to generate carbonate. Spent sorbent containing the bicarbonate or carbonate is moved to a second reactor where it is heated or treated with a reducing agent such as, natural gas, methane, carbon monoxide hydrogen, or a synthesis gas comprising of a combination of carbon monoxide and hydrogen. The heat or reducing agent releases carbon dioxide gas and regenerates the active material for use as the sorbent material in the first reactor. New sorbent may be added to the regenerated sorbent prior to subsequent passes in the carbon dioxide removal reactor.

  2. Carbon dioxide capture from a cement manufacturing process

    DOEpatents

    Blount, Gerald C.; Falta, Ronald W.; Siddall, Alvin A.

    2011-07-12

    A process of manufacturing cement clinker is provided in which a clean supply of CO.sub.2 gas may be captured. The process also involves using an open loop conversion of CaO/MgO from a calciner to capture CO.sub.2 from combustion flue gases thereby forming CaCO.sub.3/CaMg(CO.sub.3).sub.2. The CaCO.sub.3/CaMg(CO.sub.3).sub.2 is then returned to the calciner where CO.sub.2 gas is evolved. The evolved CO.sub.2 gas, along with other evolved CO.sub.2 gases from the calciner are removed from the calciner. The reactants (CaO/MgO) are feed to a high temperature calciner for control of the clinker production composition.

  3. Carbon dioxide capture from power or process plant gases

    SciTech Connect

    Bearden, Mark D; Humble, Paul H

    2014-06-10

    The present invention are methods for removing preselected substances from a mixed flue gas stream characterized by cooling said mixed flue gas by direct contact with a quench liquid to condense at least one preselected substance and form a cooled flue gas without substantial ice formation on a heat exchanger. After cooling additional process methods utilizing a cryogenic approach and physical concentration and separation or pressurization and sorbent capture may be utilized to selectively remove these materials from the mixed flue gas resulting in a clean flue gas.

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

    SciTech Connect

    Farnum, Rachel; Perry, Robert; Wood, Benjamin

    2014-12-31

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

  5. Novel Sorption/Desorption Process for Carbon Dioxide Capture (Feasibility Study)

    SciTech Connect

    William Tuminello; Maciej Radosz; Youqing Shen

    2008-11-01

    Western Research Institute and the University of Wyoming Enhanced Oil Recovery Institute have tested a novel approach to carbon dioxide capture in power plants and industrial operations. This approach is expected to provide considerable cost savings, in terms of regeneration of the sorbent. It is proposed that low molecular weight, low volatility liquid fluorocarbons be utilized to absorb CO{sub 2} due to their unusual affinity for the gas. The energy savings would be realized by cooling the fluorocarbon liquids below their melting point where the CO{sub 2} would be released even at elevated pressure. Thus, the expense of heating currently used sorbents, saturated with CO{sub 2}, under low pressure conditions and then having to compress the released gas would not be realized. However, these fluorinated materials have been shown to be poor carbon dioxide absorbers under conditions currently required for carbon capture. The project was terminated.

  6. Carbon Dioxide Capture and Disposal

    NASA Astrophysics Data System (ADS)

    Lackner, K. S.

    2002-05-01

    Unless carbon dioxide from fossil fuel combustion is captured and disposed of safely and permanently, the concerns over climate change will eventually lead to the demise of fossil fuels. Because of their importance in today's energy market the phasing out of fossil fuels would likely precipitate a major energy crisis. Mineral sequestration and extraction of carbon dioxide from the air are two advanced technologies for carbon sequestration that aim at maintaining access to the vast fossil energy resources for centuries to come. While it is straightforward to dispose of carbon dioxide in limited amounts and for a limited time, permanent disposal of trillions of tons of carbon poses serious challenges. The formation of solid mineral carbonates from readily available minerals would provide safe and permanent storage. Capture of carbon dioxide from air makes it possible to sequester carbon dioxide emissions from sources other than power plants. This is important considering that even the relatively minor reductions suggested by the Kyoto Accord would have required the US to eliminate carbon dioxide emissions comparable to those of the entire 1990 coal fired power plant fleet. Capture of carbon dioxide from the air, would make it possible to close the carbon cycle in the transportation sector without phasing out liquid hydrocarbon fuels. It eliminates the need for long distance transport of carbon dioxide and allows the continued use of the existing energy infrastructure. Mineral sequestration at remote sites combined with on site carbon dioxide capture from air, would allow for long term stabilization of atmospheric carbon dioxide levels. I will outline the current state of the technology and point to advances required before these approaches are ready for large-scale implementation.

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

    SciTech Connect

    Arastoopour, Hamid; Abbasian, Javad

    2014-07-31

    estimated cost of carbon v capture is in the range of $31-$44/ton, suggesting that a regenerative MgO-Based process can be a viable option for pre-combustion carbon dioxide capture in advanced gasification based power systems.

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

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

    SciTech Connect

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

    2014-07-01

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

  10. Capture of carbon dioxide by hybrid sorption

    SciTech Connect

    Srinivasachar, Srivats

    2014-09-23

    A composition, process and system for capturing carbon dioxide from a combustion gas stream. The composition has a particulate porous support medium that has a high volume of pores, an alkaline component distributed within the pores and on the surface of the support medium, and water adsorbed on the alkaline component, wherein the proportion of water in the composition is between about 5% and about 35% by weight of the composition. The process and system contemplates contacting the sorbent and the flowing gas stream together at a temperature and for a time such that some water remains adsorbed in the alkaline component when the contact of the sorbent with the flowing gas ceases.

  11. Encapsulated liquid sorbents for carbon dioxide capture.

    PubMed

    Vericella, John J; Baker, Sarah E; Stolaroff, Joshuah K; Duoss, Eric B; Hardin, James O; Lewicki, James; Glogowski, Elizabeth; Floyd, William C; Valdez, Carlos A; Smith, William L; Satcher, Joe H; Bourcier, William L; Spadaccini, Christopher M; Lewis, Jennifer A; Aines, Roger D

    2015-02-05

    Drawbacks of current carbon dioxide capture methods include corrosivity, evaporative losses and fouling. Separating the capture solvent from infrastructure and effluent gases via microencapsulation provides possible solutions to these issues. Here we report carbon capture materials that may enable low-cost and energy-efficient capture of carbon dioxide from flue gas. Polymer microcapsules composed of liquid carbonate cores and highly permeable silicone shells are produced by microfluidic assembly. This motif couples the capacity and selectivity of liquid sorbents with high surface area to facilitate rapid and controlled carbon dioxide uptake and release over repeated cycles. While mass transport across the capsule shell is slightly lower relative to neat liquid sorbents, the surface area enhancement gained via encapsulation provides an order-of-magnitude increase in carbon dioxide absorption rates for a given sorbent mass. The microcapsules are stable under typical industrial operating conditions and may be used in supported packing and fluidized beds for large-scale carbon capture.

  12. Encapsulated liquid sorbents for carbon dioxide capture

    NASA Astrophysics Data System (ADS)

    Vericella, John J.; Baker, Sarah E.; Stolaroff, Joshuah K.; Duoss, Eric B.; Hardin, James O.; Lewicki, James; Glogowski, Elizabeth; Floyd, William C.; Valdez, Carlos A.; Smith, William L.; Satcher, Joe H.; Bourcier, William L.; Spadaccini, Christopher M.; Lewis, Jennifer A.; Aines, Roger D.

    2015-02-01

    Drawbacks of current carbon dioxide capture methods include corrosivity, evaporative losses and fouling. Separating the capture solvent from infrastructure and effluent gases via microencapsulation provides possible solutions to these issues. Here we report carbon capture materials that may enable low-cost and energy-efficient capture of carbon dioxide from flue gas. Polymer microcapsules composed of liquid carbonate cores and highly permeable silicone shells are produced by microfluidic assembly. This motif couples the capacity and selectivity of liquid sorbents with high surface area to facilitate rapid and controlled carbon dioxide uptake and release over repeated cycles. While mass transport across the capsule shell is slightly lower relative to neat liquid sorbents, the surface area enhancement gained via encapsulation provides an order-of-magnitude increase in carbon dioxide absorption rates for a given sorbent mass. The microcapsules are stable under typical industrial operating conditions and may be used in supported packing and fluidized beds for large-scale carbon capture.

  13. Subsurface capture of carbon dioxide

    DOEpatents

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

    2014-07-22

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

  14. Bench-Scale Process for Low-Cost Carbon Dioxide (CO2) Capture Using a Phase-Changing Absorbent

    SciTech Connect

    Westendorf, Tiffany; Caraher, Joel; Chen, Wei; Farnum, Rachael; Perry, Robert; Spiry, Irina; Wilson, Paul; Wood, Benjamin

    2015-03-31

    The objective of this project is to design and build a bench-scale process for a novel phase-changing aminosilicone-based CO2-capture solvent. The project will establish scalability and technical and economic feasibility of using a phase-changing CO2-capture absorbent for post-combustion capture of CO2 from coal-fired power plants with 90% capture efficiency and 95% CO2 purity at a cost of $40/tonne of CO2 captured by 2025 and a cost of <$10/tonne of CO2 captured by 2035. In the first budget period of this project, the bench-scale phase-changing CO2 capture process was designed using data and operating experience generated under a previous project (ARPA-e project DE-AR0000084). Sizing and specification of all major unit operations was completed, including detailed process and instrumentation diagrams. The system was designed to operate over a wide range of operating conditions to allow for exploration of the effect of process variables on CO2 capture performance.

  15. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

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

    2001-07-01

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

  16. Pilot-Scale Silicone Process for Low-Cost Carbon Dioxide Capture Preliminary Techno-Economic Analysis

    SciTech Connect

    Singh, Surinder; Spiry, Irina; Wood, Benjamin; Hance, Dan; Chen, Wei; Kehmna, Mark; McDuffie, Dwayne

    2014-03-31

    This report presents system and economic analysis for a carbon-capture unit which uses an aminosilicone-based solvent for CO{sub 2} capture in a pulverized coal (PC) boiler. The aminosilicone solvent is a 60/40 wt/wt mixture of 3-aminopropyl end-capped polydimethylsiloxane (GAP-1m) with tri-ethylene glycol (TEG) as a co-solvent. For comparison purposes, the report also shows results for a carbon-capture unit based on a conventional approach using mono-ethanol amine (MEA). The first year removal cost of CO{sub 2} for the aminosilicone-based carbon-capture process is $46.04/ton of CO2 as compared to $60.25/ton of CO{sub 2} when MEA is used. The aminosilicone-based process has <77% of the CAPEX of a system using MEA solvent. The lower CAPEX is due to several factors, including the higher working capacity of the aminosilicone solvent compared the MEA, which reduces the solvent flow rate required, reducing equipment sizes. If it is determined that carbon steel can be used in the rich-lean heat exchanger in the carbon capture unit, the first year removal cost of CO{sub 2} decreases to $44.12/ton. The aminosilicone-based solvent has a higher thermal stability than MEA, allowing desorption to be conducted at higher temperatures and pressures, decreasing the number of compressor stages needed. The aminosilicone-based solvent also has a lower vapor pressure, allowing the desorption to be conducted in a continuous-stirred tank reactor versus a more expensive packed column. The aminosilicone-based solvent has a lower heat capacity, which decreases the heat load on the desorber. In summary, the amino-silicone solvent has significant advantages over conventional systems using MEA.

  17. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Thomas Nelson

    2004-07-01

    This report describes research conducted between April 1, 2004 and June 30, 2004 on the preparation and use of dry regenerable sorbents for removal of carbon dioxide from flue gas. Support materials and supported sorbents were prepared by spray drying. Sorbents consisting of 20 to 50% sodium carbonate on a ceramic support were prepared by spray drying in batches of approximately 300 grams. The supported sorbents exhibited greater carbon dioxide capture rates than unsupported calcined sodium bicarbonate in laboratory tests. Preliminary process design and cost estimation for a retrofit application suggested that costs of a dry regenerable sodium carbonate-based process could be lower than those of a monoethanolamine absorption system. In both cases, the greatest part of the process costs come from power plant output reductions due to parasitic consumption of steam for recovery of carbon dioxide from the capture medium.

  18. Capture of green-house carbon dioxide in Portland cement

    SciTech Connect

    Wagh, A.S.; Singh, D.; Pullockaran, J.; Knox, L.

    1993-12-31

    A novel process has been developed to sequester green-house carbon dioxide produced by the cement industry in precast cement products. Typically, 10--24 wt % of CO{sub 2} produced by calcination of calcium carbonate during clinkering of the cement may be captured. The carbonation process also cures the cement paste within minutes into hard bodies. The process maintains high pH conditions during curing, to allow conventional steel reinforcement of concrete. The process will save time and money to the cement industry, and at the same time, help them to comply with the Clean Air Act by sequestering the green-house carbon dioxide.

  19. Designed amyloid fibers as materials for selective carbon dioxide capture.

    PubMed

    Li, Dan; Furukawa, Hiroyasu; Deng, Hexiang; Liu, Cong; Yaghi, Omar M; Eisenberg, David S

    2014-01-01

    New materials capable of binding carbon dioxide are essential for addressing climate change. Here, we demonstrate that amyloids, self-assembling protein fibers, are effective for selective carbon dioxide capture. Solid-state NMR proves that amyloid fibers containing alkylamine groups reversibly bind carbon dioxide via carbamate formation. Thermodynamic and kinetic capture-and-release tests show the carbamate formation rate is fast enough to capture carbon dioxide by dynamic separation, undiminished by the presence of water, in both a natural amyloid and designed amyloids having increased carbon dioxide capacity. Heating to 100 °C regenerates the material. These results demonstrate the potential of amyloid fibers for environmental carbon dioxide capture.

  20. A new porous material to enhance the kinetics of clathrate process: application to precombustion carbon dioxide capture.

    PubMed

    Babu, Ponnivalavan; Kumar, Rajnish; Linga, Praveen

    2013-11-19

    In this work, the performance of a new porous medium, polyurethane (PU) foam in a fixed bed reactor for carbon dioxide separation from fuel gas mixture using the hydrate based gas separation process is evaluated. The kinetics of hydrate formation in the presence of 2.5 mol % propane as thermodynamic promoter was investigated at 4.5, 5.5, and 6.0 MPa and 274.2 K. Significantly higher gas consumption and water conversion to hydrate was achieved when PU foam was employed. PU foam as a porous medium can help convert 54% of water to hydrate in two hours of hydrate formation. In addition the induction times were very low (<3.67 min at 6.0 MPa). A normalized rate of hydrate formation of 64.48 (±3.82) mol x min(-1) x m(-3) was obtained at 6.0 MPa and 274.2 K. Based on a morphological study, the mechanism of hydrate formation from water dispersed in interstitial pore space of the porous medium is presented. Finally, we propose a four step operation of the hydrate based gas separation process to scale up.

  1. Development of a Steel-Slag-Based, Iron-Functionalized Sorbent for an Autothermal Carbon Dioxide Capture Process.

    PubMed

    Tian, Sicong; Jiang, Jianguo; Hosseini, Davood; Kierzkowska, Agnieszka M; Imtiaz, Qasim; Broda, Marcin; Müller, Christoph R

    2015-11-01

    We propose a new class of autothermal CO2 -capture process that relies on the integration of chemical looping combustion (CLC) into calcium looping (CaL). In the new process, the heat released during the oxidation of a reduced metallic oxide is utilized to drive the endothermic calcination of CaCO3 (the regeneration step in CaL). Such a process is potentially very attractive (both economically and technically) as it can be applied to a variety of oxygen carriers and CaO is not in direct contact with coal (and the impurities associated with it) in the calciner (regeneration step). To demonstrate the practical feasibility of the process, we developed a low-cost, steel-slag-based, Fe-functionalized CO2 sorbent. Using this material, we confirm experimentally the feasibility to heat-integrate CaCO3 calcination with a Fe(II)/Fe(III) redox cycle (with regards to the heat of reaction and kinetics). The autothermal calcination of CaCO3 could be achieved for a material that contained a Ca/Fe ratio of 5:4. The uniform distribution of Ca and Fe in a solid matrix provides excellent heat transfer characteristics. The cyclic CO2 uptake and redox stability of the material is good, but there is room for further improvement.

  2. Development of a Steel-Slag-Based, Iron-Functionalized Sorbent for an Autothermal Carbon Dioxide Capture Process.

    PubMed

    Tian, Sicong; Jiang, Jianguo; Hosseini, Davood; Kierzkowska, Agnieszka M; Imtiaz, Qasim; Broda, Marcin; Müller, Christoph R

    2015-11-01

    We propose a new class of autothermal CO2 -capture process that relies on the integration of chemical looping combustion (CLC) into calcium looping (CaL). In the new process, the heat released during the oxidation of a reduced metallic oxide is utilized to drive the endothermic calcination of CaCO3 (the regeneration step in CaL). Such a process is potentially very attractive (both economically and technically) as it can be applied to a variety of oxygen carriers and CaO is not in direct contact with coal (and the impurities associated with it) in the calciner (regeneration step). To demonstrate the practical feasibility of the process, we developed a low-cost, steel-slag-based, Fe-functionalized CO2 sorbent. Using this material, we confirm experimentally the feasibility to heat-integrate CaCO3 calcination with a Fe(II)/Fe(III) redox cycle (with regards to the heat of reaction and kinetics). The autothermal calcination of CaCO3 could be achieved for a material that contained a Ca/Fe ratio of 5:4. The uniform distribution of Ca and Fe in a solid matrix provides excellent heat transfer characteristics. The cyclic CO2 uptake and redox stability of the material is good, but there is room for further improvement. PMID:26616682

  3. Layered solid sorbents for carbon dioxide capture

    SciTech Connect

    Li, Bingyun; Jiang, Bingbing; Gray, McMahan L; Fauth, Daniel J; Pennline, Henry W; Richards, George A

    2014-11-18

    A solid sorbent for the capture and the transport of carbon dioxide gas is provided having at least one first layer of a positively charged material that is polyethylenimine or poly(allylamine hydrochloride), that captures at least a portion of the gas, and at least one second layer of a negatively charged material that is polystyrenesulfonate or poly(acryclic acid), that transports the gas, wherein the second layer of material is in juxtaposition to, attached to, or crosslinked with the first layer for forming at least one bilayer, and a solid substrate support having a porous surface, wherein one or more of the bilayers is/are deposited on the surface of and/or within the solid substrate. A method of preparing and using the solid sorbent is provided.

  4. Sulfur Dioxide Capture by Heterogeneous Oxidation on Hydroxylated Manganese Dioxide.

    PubMed

    Wu, Haodong; Cai, Weimin; Long, Mingce; Wang, Hairui; Wang, Zhiping; Chen, Chen; Hu, Xiaofang; Yu, Xiaojuan

    2016-06-01

    Here we demonstrate that sulfur dioxide (SO2) is efficiently captured via heterogeneous oxidation into sulfate on the surface of hydroxylated manganese dioxide (MnO2). Lab-scale activity tests in a fluidized bed reactor showed that the removal efficiency for a simulated flue gas containing 5000 mg·Nm(-3) SO2 could reach nearly 100% with a GHSV (gas hourly space velocity) of 10000 h(-1). The mechanism was investigated using a combination of experimental characterizations and theoretical calculations. It was found that formation of surface bound sulfate proceeds via association of SO2 with terminal hydroxyls. Both H2O and O2 are essential for the generation of reactive terminal hydroxyls, and the indirect role of O2 in heterogeneous SO2 oxidation at low temperature was also revealed. We propose that the high reactivity of terminal hydroxyls is attributed to the proper surface configuration of MnO2 to adsorb water with degenerate energies for associative and dissociative states, and maintain rapid proton dynamics. Viability analyses suggest that the desulfurization method that is based on such a direct oxidation reaction at the gas/solid interface represents a promising approach for SO2 capture. PMID:27123922

  5. Carbon dioxide removal process

    DOEpatents

    Baker, Richard W.; Da Costa, Andre R.; Lokhandwala, Kaaeid A.

    2003-11-18

    A process and apparatus for separating carbon dioxide from gas, especially natural gas, that also contains C.sub.3+ hydrocarbons. The invention uses two or three membrane separation steps, optionally in conjunction with cooling/condensation under pressure, to yield a lighter, sweeter product natural gas stream, and/or a carbon dioxide stream of reinjection quality and/or a natural gas liquids (NGL) stream.

  6. Biochemical Capture and Removal of Carbon Dioxide

    NASA Technical Reports Server (NTRS)

    Trachtenberg, Michael C.

    1998-01-01

    We devised an enzyme-based facilitated transport membrane bioreactor system to selectively remove carbon dioxide (CO2) from the space station environment. We developed and expressed site-directed enzyme mutants for CO2 capture. Enzyme kinetics showed the mutants to be almost identical to the wild type save at higher pH. Both native enzyme and mutant enzymes were immobilized to different supports including nylons, glasses, sepharose, methacrylate, titanium and nickel. Mutant enzyme could be attached and removed from metal ligand supports and the supports reused at least five times. Membrane systems were constructed to test CO2 selectivity. These included proteic membranes, thin liquid films and enzyme-immobilized teflon membranes. Selectivity ratios of more than 200:1 were obtained for CO2 versus oxygen with CO2 at 0.1%. The data indicate that a membrane based bioreactor can be constructed which could bring CO2 levels close to Earth.

  7. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Thomas Nelson; Brian S. Turk; Paul Box; Weijiong Li; Raghubir P. Gupta

    2005-07-01

    This report describes research conducted between April 1, 2005 and June 30, 2005 on the use of dry regenerable sorbents for removal of carbon dioxide from flue gas from coal combustion and synthesis gas from coal gasification. Supported sodium carbonate sorbents removed up to 76% of the carbon dioxide from simulated flue gas in a downflow cocurrent flow reactor system, with an approximate 15 second gas-solid contact time. This reaction proceeds at temperatures as low as 25 C. Lithium silicate sorbents remove carbon dioxide from high temperature simulated flue gas and simulated synthesis gas. Both sorbent types can be thermally regenerated and reused. The lithium silicate sorbent was tested in a thermogravimetric analyzer and in a 1-in quartz reactor at atmospheric pressure; tests were also conducted at elevated pressure in a 2-in diameter high temperature high pressure reactor system. The lithium sorbent reacts rapidly with carbon dioxide in flue gas at 350-500 C to absorb about 10% of the sorbent weight, then continues to react at a lower rate. The sorbent can be essentially completely regenerated at temperatures above 600 C and reused. In atmospheric pressure tests with synthesis gas of 10% initial carbon dioxide content, the sorbent removed over 90% of the carbon dioxide. An economic analysis of a downflow absorption process for removal of carbon dioxide from flue gas with a supported sodium carbonate sorbent suggests that a 90% efficient carbon dioxide capture system installed at a 500 MW{sub e} generating plant would have an incremental capital cost of $35 million ($91/kWe, assuming 20 percent for contingencies) and an operating cost of $0.0046/kWh. Assuming capital costs of $1,000/kW for a 500 MWe plant the capital cost of the down flow absorption process represents a less than 10% increase, thus meeting DOE goals as set forth in its Carbon Sequestration Technology Roadmap and Program Plan.

  8. Amine reclaiming technologies in post-combustion carbon dioxide capture.

    PubMed

    Wang, Tielin; Hovland, Jon; Jens, Klaus J

    2015-01-01

    Amine scrubbing is the most developed technology for carbon dioxide (CO2) capture. Degradation of amine solvents due to the presence of high levels of oxygen and other impurities in flue gas causes increasing costs and deterioration in long term performance, and therefore purification of the solvents is needed to overcome these problems. This review presents the reclaiming of amine solvents used for post combustion CO2 capture (PCC). Thermal reclaiming, ion exchange, and electrodialysis, although principally developed for sour gas sweetening, have also been tested for CO2 capture from flue gas. The three technologies all have their strengths and weaknesses, and further development is needed to reduce energy usage and costs. An expected future trend for amine reclamation is to focus on process integration of the current reclaiming technologies into the PCC process in order to drive down costs.

  9. Designed amyloid fibers as materials for selective carbon dioxide capture

    PubMed Central

    Li, Dan; Furukawa, Hiroyasu; Deng, Hexiang; Liu, Cong; Yaghi, Omar M.; Eisenberg, David S.

    2014-01-01

    New materials capable of binding carbon dioxide are essential for addressing climate change. Here, we demonstrate that amyloids, self-assembling protein fibers, are effective for selective carbon dioxide capture. Solid-state NMR proves that amyloid fibers containing alkylamine groups reversibly bind carbon dioxide via carbamate formation. Thermodynamic and kinetic capture-and-release tests show the carbamate formation rate is fast enough to capture carbon dioxide by dynamic separation, undiminished by the presence of water, in both a natural amyloid and designed amyloids having increased carbon dioxide capacity. Heating to 100 °C regenerates the material. These results demonstrate the potential of amyloid fibers for environmental carbon dioxide capture. PMID:24367077

  10. Self-Assembled Enzyme Nanoparticles for Carbon Dioxide Capture.

    PubMed

    Shanbhag, Bhuvana Kamath; Liu, Boyin; Fu, Jing; Haritos, Victoria S; He, Lizhong

    2016-05-11

    Enzyme-based processes have shown promise as a sustainable alternative to amine-based processes for carbon dioxide capture. In this work, we have engineered carbonic anhydrase nanoparticles that retain 98% of hydratase activity in comparison to their free counterparts. Carbonic anhydrase was fused with a self-assembling peptide that facilitates the noncovalent assembly of the particle and together were recombinantly expressed from a single gene construct in Escherichia coli. The purified enzymes, when subjected to a reduced pH, form 50-200 nm nanoparticles. The CO2 capture capability of enzyme nanoparticles was demonstrated at ambient (22 ± 2 °C) and higher (50 °C) temperatures, under which the nanoparticles maintain their assembled state. The carrier-free enzymatic nanoparticles demonstrated here offer a new approach to stabilize and reuse enzymes in a simple and cost-effective manner.

  11. Calcium looping process for high purity hydrogen production integrated with capture of carbon dioxide, sulfur and halides

    DOEpatents

    Ramkumar, Shwetha; Fan, Liang-Shih

    2013-07-30

    A process for producing hydrogen comprising the steps of: (i) gasifying a fuel into a raw synthesis gas comprising CO, hydrogen, steam, sulfur and halide contaminants in the form of H.sub.2S, COS, and HX, wherein X is a halide; (ii) passing the raw synthesis gas through a water gas shift reactor (WGSR) into which CaO and steam are injected, the CaO reacting with the shifted gas to remove CO.sub.2, sulfur and halides in a solid-phase calcium-containing product comprising CaCO.sub.3, CaS and CaX.sub.2; (iii) separating the solid-phase calcium-containing product from an enriched gaseous hydrogen product; and (iv) regenerating the CaO by calcining the solid-phase calcium-containing product at a condition selected from the group consisting of: in the presence of steam, in the presence of CO.sub.2, in the presence of synthesis gas, in the presence of H.sub.2 and O.sub.2, under partial vacuum, and combinations thereof.

  12. Calcium looping process for high purity hydrogen production integrated with capture of carbon dioxide, sulfur and halides

    DOEpatents

    Ramkumar, Shwetha; Fan, Liang-Shih

    2015-11-04

    A process for producing hydrogen comprising the steps of: (i) gasifying a fuel into a raw synthesis gas comprising CO, hydrogen, steam, sulfur and halide contaminants in the form of H.sub.2S, COS, and HX, wherein X is a halide; (ii) passing the raw synthesis gas through a water gas shift reactor (WGSR) into which CaO and steam are injected, the CaO reacting with the shifted gas to remove CO.sub.2, sulfur and halides in a solid-phase calcium-containing product comprising CaCO.sub.3, CaS and CaX.sub.2; (iii) separating the solid-phase calcium-containing product from an enriched gaseous hydrogen product; and (iv) regenerating the CaO by calcining the solid-phase calcium-containing product at a condition selected from the group consisting of: in the presence of steam, in the presence of CO.sub.2, in the presence of synthesis gas, in the presence of H.sub.2 and O.sub.2, under partial vacuum, and combinations thereof.

  13. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Ya Liang; Tyler Moore; Douglas P. Harrison

    2003-08-01

    This report describes research conducted between April 1, 2003 and June 30, 2003 on the use of dry regenerable sorbents for concentration of carbon dioxide from flue gas. Grade 1 sodium bicarbonate performed similarly to grade 5 sodium bicarbonate in fixed bed testing in that activity improved after the first carbonation cycle and did not decline over the course of 5 cycles. Thermogravimetric analysis indicated that sodium bicarbonate sorbents produced by calcination of sodium bicarbonate are superior to either soda ash or calcined trona. Energy requirements for regeneration of carbon dioxide sorbents (either wet or dry) is of primary importance in establishing the economic feasibility of carbon dioxide capture processes. Recent studies of liquid amine sorption processes were reviewed and found to incorporate conflicting assumptions of energy requirements. Dry sodium based processes have the potential to be less energy intensive and thus less expensive than oxygen inhibited amine based systems. For dry supported sorbents, maximizing the active fraction of the sorbent is of primary importance in developing an economically feasible process.

  14. Carbon dioxide capture and use: organic synthesis using carbon dioxide from exhaust gas.

    PubMed

    Kim, Seung Hyo; Kim, Kwang Hee; Hong, Soon Hyeok

    2014-01-13

    A carbon capture and use (CCU) strategy was applied to organic synthesis. Carbon dioxide (CO2) captured directly from exhaust gas was used for organic transformations as efficiently as hyper-pure CO2 gas from a commercial source, even for highly air- and moisture-sensitive reactions. The CO2 capturing aqueous ethanolamine solution could be recycled continuously without any diminished reaction efficiency.

  15. Sulfur dioxide removal process

    SciTech Connect

    Sliger, A.G.; O'Donnell, J.J.; Northup, A.H. Jr.

    1987-01-06

    A process is described for removing sulfur dioxide from a gas stream with a buffered, aqueous thiosulfate/polythionate solution which comprises: (a) introducing sulfur dioxide-containing gas, recovered hydrogen sulfide, and a buffered, aqueous, lean thiosulfate/polythionate solution to an SO/sub 2/-gas/liquid contacting zone; (b) recovering cleaned gas and a buffered, aqueous, enriched thiosulfate/polythionate solution from the SO/sub 2/-gas/liquid contacting zone; (c) introducing the recovered, enriched solution to a regeneration zone; (d) introducing externally supplied hydrogen sulfide to the regeneration zone to react a portion of the recovered, enriched solution therein to form a slurry of elemental sulfur in a buffered, aqueous, lean thiosulfate/polythionate solution; (e) recovering unreacted excess hydrogen sulfide from the regeneration zone for use in step (a); and (f) withdrawing the slurry from the regeneration zone, separating elemental sulfur from the slurry, and recovering the buffered, aqueous, lean thiosulfate/polythionate solution for use in step (a).

  16. Direct Electrochemical Capture and Release of Carbon Dioxide Using an Industrial Organic Pigment: Quinacridone**

    PubMed Central

    Apaydin, Dogukan Hazar; Głowacki, Eric Daniel; Portenkirchner, Engelbert; Sariciftci, Niyazi Serdar

    2014-01-01

    Limiting anthropogenic carbon dioxide emissions constitutes a major issue faced by scientists today. Herein we report an efficient way of controlled capture and release of carbon dioxide using nature inspired, cheap, abundant and non-toxic, industrial pigment namely, quinacridone. An electrochemically reduced electrode consisting of a quinacridone thin film (ca. 100 nm thick)on an ITO support forms a quinacridone carbonate salt. The captured CO2 can be released by electrochemical oxidation. The amount of captured CO2 was quantified by FT-IR. The uptake value for electrochemical release process was 4.61 mmol g−1. This value is among the highest reported uptake efficiencies for electrochemical CO2 capture. For comparison, the state-of-the-art aqueous amine industrial capture process has an uptake efficiency of ca. 8 mmol g−1. PMID:24849072

  17. Direct electrochemical capture and release of carbon dioxide using an industrial organic pigment: quinacridone.

    PubMed

    Apaydin, Dogukan Hazar; Głowacki, Eric Daniel; Portenkirchner, Engelbert; Sariciftci, Niyazi Serdar

    2014-06-23

    Limiting anthropogenic carbon dioxide emissions constitutes a major issue faced by scientists today. Herein we report an efficient way of controlled capture and release of carbon dioxide using nature inspired, cheap, abundant and non-toxic, industrial pigment namely, quinacridone. An electrochemically reduced electrode consisting of a quinacridone thin film (ca. 100 nm thick) on an ITO support forms a quinacridone carbonate salt. The captured CO2 can be released by electrochemical oxidation. The amount of captured CO2 was quantified by FT-IR. The uptake value for electrochemical release process was 4.61 mmol g(-1). This value is among the highest reported uptake efficiencies for electrochemical CO2 capture. For comparison, the state-of-the-art aqueous amine industrial capture process has an uptake efficiency of ca. 8 mmol g(-1).

  18. Carbon Dioxide Capture and Transportation Options in the Illinois Basin

    SciTech Connect

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

    2004-09-30

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

  19. Designing and Demonstrating a Master Student Project to Explore Carbon Dioxide Capture Technology

    ERIC Educational Resources Information Center

    Asherman, Florine; Cabot, Gilles; Crua, Cyril; Estel, Lionel; Gagnepain, Charlotte; Lecerf, Thibault; Ledoux, Alain; Leveneur, Sebastien; Lucereau, Marie; Maucorps, Sarah; Ragot, Melanie; Syrykh, Julie; Vige, Manon

    2016-01-01

    The rise in carbon dioxide (CO[subscript 2]) concentration in the Earth's atmosphere, and the associated strengthening of the greenhouse effect, requires the development of low carbon technologies. New carbon capture processes are being developed to remove CO[subscript 2] that would otherwise be emitted from industrial processes and fossil fuel…

  20. Atmospheric CO2 capture by algae: Negative carbon dioxide emission path.

    PubMed

    Moreira, Diana; Pires, José C M

    2016-09-01

    Carbon dioxide is one of the most important greenhouse gas, which concentration increase in the atmosphere is associated to climate change and global warming. Besides CO2 capture in large emission point sources, the capture of this pollutant from atmosphere may be required due to significant contribution of diffuse sources. The technologies that remove CO2 from atmosphere (creating a negative balance of CO2) are called negative emission technologies. Bioenergy with Carbon Capture and Storage may play an important role for CO2 mitigation. It represents the combination of bioenergy production and carbon capture and storage, keeping carbon dioxide in geological reservoirs. Algae have a high potential as the source of biomass, as they present high photosynthetic efficiencies and high biomass yields. Their biomass has a wide range of applications, which can improve the economic viability of the process. Thus, this paper aims to assess the atmospheric CO2 capture by algal cultures.

  1. Atmospheric CO2 capture by algae: Negative carbon dioxide emission path.

    PubMed

    Moreira, Diana; Pires, José C M

    2016-09-01

    Carbon dioxide is one of the most important greenhouse gas, which concentration increase in the atmosphere is associated to climate change and global warming. Besides CO2 capture in large emission point sources, the capture of this pollutant from atmosphere may be required due to significant contribution of diffuse sources. The technologies that remove CO2 from atmosphere (creating a negative balance of CO2) are called negative emission technologies. Bioenergy with Carbon Capture and Storage may play an important role for CO2 mitigation. It represents the combination of bioenergy production and carbon capture and storage, keeping carbon dioxide in geological reservoirs. Algae have a high potential as the source of biomass, as they present high photosynthetic efficiencies and high biomass yields. Their biomass has a wide range of applications, which can improve the economic viability of the process. Thus, this paper aims to assess the atmospheric CO2 capture by algal cultures. PMID:27005790

  2. Sulphur dioxide removal process

    SciTech Connect

    Flintoff, J.F.

    1980-06-10

    Sodium sulfate is purged from a sulfur dioxide removal system involving contact of a sulfur dioxide-containing gas with a solution containing sodium sulfite to absorb sulfur dioxide from the gas. The spent absorbing solution is regenerated by desorbing sulfur dioxide, and recycled for further use. To avoid an unduly large build-up of sulfate in the system, a portion of the absorbing-desorbing medium, e.g., spent absorbing solution, containing sodium sulfate, a relatively large amount of sodium bisulfite, and generally a minor amount of sodium sulfite, is treated to precipitate solids containing sodium sulfate in a concentration which is greater on a dry basis than would otherwise be obtained in the absorption-desorption cycle. The concentration of sodium sulfate in the precipitated solids is increased by providing a portion of the precipitated sodium sulfate-containing solids, e.g., about 25 to 75 weight percent, in solution in the absorbing-desorbing medium treated for sulfate removal. Preferably, sulfate removal is accomplished by reducing the amount of water in the portion of the absorbing-desorbing medium treated so that only sufficient solids are precipitated from said medium to comprise up to about 10, or up to about 20, weight percent of the medium.

  3. Carbon Capture by a Continuous, Regenerative Ammonia-Based Scrubbing Process

    SciTech Connect

    Resnik, K.P.; Yeh, J.T.; Pennline, H.W.

    2006-10-01

    Overview: To develop a knowledge/data base to determine whether an ammonia-based scrubbing process is a viable regenerable-capture technique that can simultaneously remove carbon dioxide, sulfur dioxide, nitric oxides, and trace pollutants from flue gas.

  4. Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents

    SciTech Connect

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

    2007-06-30

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

  5. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Thomas Nelson

    2004-11-01

    Laboratory studies were conducted to investigate dry, regenerable, alkali carbonate-based sorbents for the capture of CO{sub 2} from power plant flue gas. Electrobalance, fixed-bed and fluid-bed reactors were used to examine both the CO{sub 2} capture and sorbent regeneration phases of the process. Sodium carbonate-based sorbents (calcined sodium bicarbonate and calcined trona) were the primary focus of the testing. Supported sodium carbonate and potassium carbonate sorbents were also tested. Sodium carbonate reacts with CO{sub 2} and water vapor contained in flue gas at temperatures between 60 and 80 C to form sodium bicarbonate, or an intermediate salt (Wegscheider's salt). Thermal regeneration of this sorbent produces an off-gas containing equal molar quantities of CO{sub 2} and H{sub 2}O. The low temperature range in which the carbonation reaction takes place is suited to treatment of coal-derived flue gases following wet flue gas desulfurization processes, but limits the concentration of water vapor which is an essential reactant in the carbonation reaction. Sorbent regeneration in an atmosphere of CO{sub 2} and water vapor can be carried out at a temperature of 160 C or higher. Pure CO{sub 2} suitable for use or sequestration is available after condensation of the H{sub 2}O. Flue gas contaminants such as SO{sub 2} react irreversibly with the sorbent so that upstream desulfurization will be required when sulfur-containing fossil fuels are used. Approximately 90% CO{sub 2} capture from a simulated flue gas was achieved during the early stages of fixed-bed reactor tests using a nominal carbonation temperature of 60 C. Effectively complete sorbent carbonation is possible when the fixed-bed test is carried out to completion. No decrease in sorbent activity was noted in a 15-cycle test using the above carbonation conditions coupled with regeneration in pure CO{sub 2} at 160 C. Fluidized-bed reactor tests of up to five cycles were conducted. Carbonation of sodium

  6. Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Thomas Nelson; Santosh Gangwal; Ya Liang; Tyler Moore; Margaret Williams; Douglas P. Harrison

    2004-09-30

    Laboratory studies were conducted to investigate dry, regenerable, alkali carbonate-based sorbents for the capture of CO{sub 2} from power plant flue gas. Electrobalance, fixed-bed and fluid-bed reactors were used to examine both the CO{sub 2} capture and sorbent regeneration phases of the process. Sodium carbonate-based sorbents (calcined sodium bicarbonate and calcined trona) were the primary focus of the testing. Supported sodium carbonate and potassium carbonate sorbents were also tested. Sodium carbonate reacts with CO{sub 2} and water vapor contained in flue gas at temperatures between 60 and 80 C to form sodium bicarbonate, or an intermediate salt (Wegscheider's salt). Thermal regeneration of this sorbent produces an off-gas containing equal molar quantities of CO{sub 2} and H{sub 2}O. The low temperature range in which the carbonation reaction takes place is suited to treatment of coal-derived flue gases following wet flue gas desulfurization processes, but limits the concentration of water vapor which is an essential reactant in the carbonation reaction. Sorbent regeneration in an atmosphere of CO{sub 2} and water vapor can be carried out at a temperature of 160 C or higher. Pure CO{sub 2} suitable for use or sequestration is available after condensation of the H{sub 2}O. Flue gas contaminants such as SO{sub 2} react irreversibly with the sorbent so that upstream desulfurization will be required when sulfur-containing fossil fuels are used. Approximately 90% CO{sub 2} capture from a simulated flue gas was achieved during the early stages of fixed-bed reactor tests using a nominal carbonation temperature of 60 C. Effectively complete sorbent carbonation is possible when the fixed-bed test is carried out to completion. No decrease in sorbent activity was noted in a 15-cycle test using the above carbonation conditions coupled with regeneration in pure CO{sub 2} at 160 C. Fluidized-bed reactor tests of up to five cycles were conducted. Carbonation of sodium

  7. PRELIMINARY TECHNICAL AND ECONOMIC FEASIBILITY STUDY ON THE INTEGRATION OF A PROCESS UTILIZING LOW-ENERGY SOLVENTS FOR CARBON DIOXIDE CAPTURE ENABLED BY A COMBINATION OF ENZYMES AND ULTRASONICS WITH A SUBCRITICAL PC POWER PLANT

    SciTech Connect

    Swaminathan, Saravanan; Kuczynska, Agnieszka; Hume, Scott; Mulgundmath, Vinay; Freeman, Charles; Bearden, Mark; Remias, Joe; Ambedkar, Balraj; Salmon, Sonja; House, Alan

    2012-11-01

    The results of the preliminary techno-economic assessment for integrating a process utilizing low-energy solvents for carbon dioxide (CO2) capture enabled by a combination of enzymes and ultrasonics with a subcritical pulverized coal (PC) power plant are presented. Four cases utilizing the enzyme-activated solvent are compared using different methodologies of regeneration against the DOE/NETL reference MEA case. The results are shown comparing the energy demand for post-combustion CO2 capture and the net higher heating value (HHV) efficiency of the power plant integrated with the post-combustion capture (PCC) plant. A levelized cost of electricity (LCOE) assessment was performed showing the costs of the options presented in the study. The key factors contributing to the reduction of LCOE were identified as enzyme make-up rate and the capability of the ultrasonic regeneration process. The net efficiency of the integrated PC power plant with CO2 capture changes from 24.9% with the reference Case 10 plant to between 24.34% and 29.97% for the vacuum regeneration options considered, and to between 26.63% and 31.41% for the ultrasonic regeneration options. The evaluation also shows the effect of the critical parameters on the LCOE, with the main variable being the initial estimation of enzyme dosing rate. The LCOE ($/MWh) values range from 112.92 to 125.23 for the vacuum regeneration options and from 108.9 to 117.50 for the ultrasonic regeneration cases considered in comparison to 119.6 for the reference Case 10. A sensitivity analysis of the effect of critical parameters on the LCOE was also performed. The results from the preliminary techno-economic assessment show that the proposed technology can be investigated further with a view to being a viable alternative to conventional CO2 scrubbing technologies.

  8. Rapid setting of portland cement by greenhouse carbon dioxide capture

    SciTech Connect

    Wagh, A.S.; Singh, D.; Knox, L.J.

    1994-04-01

    Following the work by Berger et al. on rapid setting of calcium silicates by carbonation, a method of high-volume capture of CO{sub 2} in portland cement has been developed. Typically, 10--24 wt. % of CO{sub 2} produced by the calcination of calcium carbonate during clinkering, may be captured, and the set cement acquires most of its full strength in less than a day. The approach will have economic advantages in fabrication of precast structures, in emergency development of infrastructure during natural disasters, and in defense applications. Moreover, it will help the cement industry comply with the Clean Air Act of 1990 by sequestering the greenhouse carbon dioxide.

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

    SciTech Connect

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

    2014-12-31

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

  10. Modeling Carbon Dioxide Capture by Monoethanolamine Solvent with ASPEN Plus

    NASA Astrophysics Data System (ADS)

    Luo, Tianyi

    Fossil fuels provide approximately 80% of the world's energy demands. Methods for reducing CO2 emissions resulting from fossil fuels include increasing the efficiency of power plants and production processes, decreasing energy demands, in combination with CO2 capture and long term storage (CCS). CO2 capture technologies include post-combustion, pre-combustion, and oxyfuel combustion. The amine-based post-combustion CO2 capture from a coal-fired power plant was studied in this thesis. In case of post-combustion capture, CO2 can be captured by Monoethanolamine solvent (MEA), a primary ethanolamine. MEA can associate with H3O+ to form an ion MEAH+, and can react with CO2 to form a carbonate ion MEACOO-. Commercial code ASPEN Plus was used to simulate the process of CO2 capture and optimize the process parameters and required energy duty. The major part of thermal energy requirement is from the Absorber and Stripper columns. This suggests that process optimization should focus on the Absorption/Desorption process. Optimization results show that the gas-liquid reaction equilibrium is affected by several operating parameters including solvent flow rate, stream temperature, column operating pressure, flue gas composition, solvent concentration and absorber design. With optimized CO2 capture, the energy consumption for solvent regeneration (reboiler thermal duty) was decreased from 5.76 GJ/ton captured CO2 to 4.56 GJ/t CO2. On the other hand, the cost of CO2 capture (and sequestration) could be reduced by limiting size of the Absorber column and operating pressure.

  11. High-Performance Sorbents for Carbon Dioxide Capture from Air

    SciTech Connect

    Sholl, David; Jones, Christopher

    2013-03-13

    This project has focused on capture of CO{sub 2} from ambient air (“air capture”). If this process is technically and economically feasible, it could potentially contribute to net reduction of CO{sub 2} emissions in ways that are complementary to better developed techniques for CO{sub 2} from concentrated point sources. We focused on cyclic adsorption processes for CO{sub 2} capture from air in which the entire cycle is performed at moderate temperatures. The project involved both experimental studies of sorbent materials and process level modeling of cyclic air capture processes. In our experimental work, a series of amine-functionalized silica adsorbents were prepared and characterized to determine the impact of molecular architecture on CO{sub 2} capture. Some key findings were: • Amine functionalized silicas can be prepared with high enough CO{sub 2} capacities under ambient conditions to merit consideration for use in air capture processes. • Primary amines are better candidates for CO{sub 2} capture than secondary or tertiary amines, both in terms of amine efficiency for CO{sub 2} adsorption and enhanced water affinity. • Mechanistic understanding of degradation of these materials can enable control of molecular architecture to significantly improve material stability. Our process modeling work provided the first publically available cost and energy estimates for cyclic adsorption processes for air capture of CO{sub 2}. Some key findings were: • Cycles based on diurnal ambient heating and cooling cannot yield useful purities or amounts of captured CO{sub 2}. • Cycles based on steam desorption at 110 oC can yield CO{sub 2} purities of ~88%. • The energy requirements for cycles using steam desorption are dominated by needs for thermal input, which results in lower costs than energy input in the form of electricity. Cyclic processes with operational costs of less than $100 tCO{sub 2}-net were described, and these results point to process and

  12. Application of halloysite nanotubes for carbon dioxide capture

    NASA Astrophysics Data System (ADS)

    Kim, Jinsoo; Rubino, Ilaria; Lee, Joo-Youp; Choi, Hyo-Jick

    2016-04-01

    Halloysite is a naturally occurring clay, with physical structure represented by halloysite nanotubes (HNTs). We investigated the potential applicability of HNTs for carbon dioxide (CO2) capture, using two amine-functionalized HNTs: (3-aminopropyl) triethoxysilane (APTES)-grafted HNTs and polyethylenimine (PEI)-impregnated HNTs. APTES-HNTs and PEI-HNTs resulted in 5.6 and 30 wt. % (in sorbent) in functionalization onto HNTs, respectively. Capture efficiency was higher in APTES-HNTs at lower temperatures, while it was maximum in PEI-HNTs at 70°C-75 °C. At 75 °C, adsorption/desorption tests showed that 95% of the two reactions occurred within 30 min, and exhibited 0.15 and 0.21 millimole of CO2 adsorption capacity per millimole of amine group for APTES-HNTs and PEI-HNTs, respectively. During 10 cycles of CO2 adsorption/desorption, there was no significant decrease in sorbent weight and adsorption capacity in both HNTs. These results show that inherent structural features of HNTs can be easily tailored for the development of operational condition-specific CO2 capture system.

  13. Process for sequestering carbon dioxide and sulfur dioxide

    DOEpatents

    Maroto-Valer, M. Mercedes; Zhang, Yinzhi; Kuchta, Matthew E.; Andresen, John M.; Fauth, Dan J.

    2009-10-20

    A process for sequestering carbon dioxide, which includes reacting a silicate based material with an acid to form a suspension, and combining the suspension with carbon dioxide to create active carbonation of the silicate-based material, and thereafter producing a metal salt, silica and regenerating the acid in the liquid phase of the suspension.

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

    SciTech Connect

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

    2013-01-01

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

  15. Carbon dioxide capture and nutrients removal utilizing treated sewage by concentrated microalgae cultivation in a membrane photobioreactor.

    PubMed

    Honda, Ryo; Boonnorat, Jarungwit; Chiemchaisri, Chart; Chiemchaisri, Wilai; Yamamoto, Kazuo

    2012-12-01

    A highly efficient microalgae cultivation process was developed for carbon dioxide capture using nutrients from treated sewage. A submerged-membrane filtration system was installed in a photobioreactor to achieve high nutrient loading and to maintain a high concentration and production of microalgae. Chlorella vulgaris, Botryococcus braunii and Spirulina platensis were continuously cultivated with simulated treated sewage and 1%-CO(2) gas. The optimum hydraulic retention time (HRT) and solids retention time (SRT) were explored to achieve the maximum CO(2) capture rate, nutrient removal rate and microalgae biomass productivity. The carbon dioxide capture rate and volumetric microalgae productivity were high when the reactor was operated under 1-day (HRT) and 18-days (SRT) conditions. The independent control of HRT and SRT is effective for efficient microalgae cultivation and carbon dioxide capture using treated sewage.

  16. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

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

    2001-05-01

    Electrobalance studies of calcination and carbonation of sodium bicarbonate materials were conducted at Louisiana State University. Calcination in an inert atmosphere was rapid and complete at 120 C. Carbonation was temperature dependent, and both the initial rate and the extent of reaction were found to decrease as temperature was increased between 60 and 80 C. A fluidization test apparatus was constructed at RTI and two sodium bicarbonate materials were fluidized in dry nitrogen at 22 C. The bed was completely fluidized at between 9 and 11 in. of water pressure drop. Kinetic rate expression derivations and thermodynamic calculations were conducted at RTI. Based on literature data, a simple reaction rate expression, which is zero order in carbon dioxide and water, was found to provide the best fit against reciprocal temperature. Simulations based on process thermodynamics suggested that approximately 26 percent of the carbon dioxide in flue gas could be recovered using waste heat available at 240 C.

  17. Thermodynamic and kinetic verification of tetra-n-butyl ammonium nitrate (TBANO3) as a promoter for the clathrate process applicable to precombustion carbon dioxide capture.

    PubMed

    Babu, Ponnivalavan; Yao, Minghuang; Datta, Stuti; Kumar, Rajnish; Linga, Praveen

    2014-03-18

    In this study, tetra-n-butyl ammonium nitrate (TBANO3) is evaluated as a promoter for precombustion capture of CO2 via hydrate formation. New hydrate phase equilibrium data for fuel gas (CO2/H2) mixture in presence of TBANO3 of various concentrations of 0.5, 1.0, 2.0, 3.0, and 3.7 mol % was determined and presented. Heat of hydrate dissociation was calculated using Clausius-Clapeyron equation and as the concentration of TBANO3 increases, the heat of hydrate dissociation also increases. Kinetic performance of TBANO3 as a promoter at different concentrations was evaluated at 6.0 MPa and 274.2 K. Based on induction time, gas uptake, separation factor, hydrate phase CO2 composition, and rate of hydrate growth, 1.0 mol % TBANO3 solution was found to be the optimum concentration at the experimental conditions of 6.0 MPa and 274.2 K for gas hydrate formation. A 93.0 mol % CO2 rich stream can be produced with a gas uptake of 0.0132 mol of gas/mol of water after one stage of hydrate formation in the presence of 1.0 mol % TBANO3 solution. Solubility measurements and microscopic images of kinetic measurements provide further insights to understand the reason for 1.0 mol % TBANO3 to be the optimum concentration.

  18. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P.Gupta; William J. McMichael; Ya Liang; Douglas P. Harrison

    2002-10-01

    The objective of this project is to develop a simple and inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable sorbent. The sorbents being investigated in this project are primarily alkali carbonates, and particularly sodium carbonate and potassium carbonate, which are converted to bicarbonates through reaction with carbon dioxide and water vapor. Bicarbonates are regenerated to carbonates when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, electrobalance tests suggested that higher temperature calcination of trona leds to reduced carbonation activity in subsequent cycles, but that calcination in dry carbon dioxide did not result in decreased activity relative to calcination in helium. Following higher temperature calcination, sodium bicarbonate (SBC) No.3 has greater activity than either coarse or fine grades of trona. Fixed bed testing of calcined SBC No.3 at 70 C confirmed that high rates of carbon dioxide absorption are possible and that the resulting product is a mixture of Wegscheider's salt and sodium carbonate. In fluidized bed testing of supported potassium carbonate, very rapid carbonation rates were observed. Activity of the support material complicated the data analysis. A milled, spherical grade of SBC appeared to be similar in attrition and abrasion characteristics to an unmilled, less regularly shaped SBC. The calcination behavior, at 107 C, for the milled and unmilled materials was also similar.

  19. Kinetic and economic analysis of reactive capture of dilute carbon dioxide with Grignard reagents.

    PubMed

    Dowson, G R M; Dimitriou, I; Owen, R E; Reed, D G; Allen, R W K; Styring, P

    2015-01-01

    Carbon Dioxide Utilisation (CDU) processes face significant challenges, especially in the energetic cost of carbon capture from flue gas and the uphill energy gradient for CO2 reduction. Both of these stumbling blocks can be addressed by using alkaline earth metal compounds, such as Grignard reagents, as sacrificial capture agents. We have investigated the performance of these reagents in their ability to both capture and activate CO2 directly from dried flue gas (essentially avoiding the costly capture process entirely) at room temperature and ambient pressures with high yield and selectivity. Naturally, to make the process sustainable, these reagents must then be recycled and regenerated. This would potentially be carried out using existing industrial processes and renewable electricity. This offers the possibility of creating a closed loop system whereby alcohols and certain hydrocarbons may be carboxylated with CO2 and renewable electricity to create higher-value products containing captured carbon. A preliminary Techno-Economic Analysis (TEA) of an example looped process has been carried out to identify the electrical and raw material supply demands and hence determine production costs. These have compared broadly favourably with existing market values.

  20. New Adsorption Cycles for Carbon Dioxide Capture and Concentration

    SciTech Connect

    James Ritter; Armin Ebner; Steven Reynolds Hai Du; Amal Mehrotra

    2008-07-31

    The objective of this three-year project was to study new pressure swing adsorption (PSA) cycles for CO{sub 2} capture and concentration at high temperature. The heavy reflux (HR) PSA concept and the use of a hydrotalcite like (HTlc) adsorbent that captures CO{sub 2} reversibly at high temperatures simply by changing the pressure were two key features of these new PSA cycles. Through the completion or initiation of nine tasks, a bench-scale experimental and theoretical program has been carried out to complement and extend the process simulation study that was carried out during Phase I (DE-FG26-03NT41799). This final report covers the entire project from August 1, 2005 to July 31, 2008. This program included the study of PSA cycles for CO{sub 2} capture by both rigorous numerical simulation and equilibrium theory analysis. The insight gained from these studies was invaluable toward the applicability of PSA for CO{sub 2} capture, whether done at ambient or high temperature. The rigorous numerical simulation studies showed that it is indeed possible to capture and concentrate CO{sub 2} by PSA. Over a wide range of conditions it was possible to achieve greater than 90% CO{sub 2} purity and/or greater than 90% CO{sub 2} recovery, depending on the particular heavy reflux (HR) PSA cycle under consideration. Three HR PSA cycles were identified as viable candidates for further study experimentally. The equilibrium theory analysis, which represents the upper thermodynamic limit of the performance of PSA process, further validated the use of certain HR PSA cycles for CO{sub 2} capture and concentration. A new graphical approach for complex PSA cycle scheduling was also developed during the course of this program. This new methodology involves a priori specifying the cycle steps, their sequence, and the number of beds, and then following a systematic procedure that requires filling in a 2-D grid based on a few simple rules, some heuristics and some experience. It has been

  1. Amine enriched solid sorbents for carbon dioxide capture

    DOEpatents

    Gray, McMahan L.; Soong, Yee; Champagne, Kenneth J.

    2003-04-15

    A new method for making low-cost CO.sub.2 sorbents that can be used in large-scale gas-solid processes. The new method entails treating a solid substrate with acid or base and simultaneous or subsequent treatment with a substituted amine salt. The method eliminates the need for organic solvents and polymeric materials for the preparation of CO.sub.2 capture systems.

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

    SciTech Connect

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

    2007-06-01

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

  3. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Raghubir P. Gupta; William J. McMichael; Douglas P. Harrison; Ya Liang

    2002-04-01

    The objective of this project is to develop a simple, inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable, sodium-based sorbent. The sorbents being investigated in this project are primarily alkali carbonates, and particularly sodium carbonate and potassium carbonate, which are converted to bicarbonates, through reaction with carbon dioxide and water vapor. Bicarbonates are regenerated to carbonates when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, electrobalance tests conducted at LSU indicated that exposure of sorbent to water vapor prior to contact with carbonation gas does not significantly increase the reaction rate. Calcined fine mesh trona has a greater initial carbonation rate than calcined sodium bicarbonate, but appears to be more susceptible to loss of reactivity under severe calcination conditions. The Davison attrition indices for Grade 5 sodium bicarbonate, commercial grade sodium carbonate and extra fine granular potassium carbonate were, as tested, outside of the range suitable for entrained bed reactor testing. Fluidized bed testing at RTI indicated that in the initial stages of reaction potassium carbonate removed 35% of the carbon dioxide in simulated flue gas, and is reactive at higher temperatures than sodium carbonate. Removals declined to 6% when 54% of the capacity of the sorbent was exhausted. Carbonation data from electrobalance testing was correlated using a shrinking core reaction model. The activation energy of the reaction of sodium carbonate with carbon dioxide and water vapor was determined from nonisothermal thermogravimetry.

  4. Enhanced Carbonate Weathering: Helping Nature Capture and Sequester Carbon Dioxide

    NASA Astrophysics Data System (ADS)

    Rau, G. H.; Rau, G. H.; Knauss, K. G.; Caldeira, K.

    2001-12-01

    Various methods have been proposed for mitigating anthropogenic CO2 release to the atmosphere, including ocean storage via enhanced biological uptake and via deep-sea injection of captured CO2. We propose an alternate capture and sequestration method that we believe would be less expensive and more environmentally friendly than the proceeding methods. Specifically, it is suggested that CO2-rich power-plant gases be hydrated with seawater to produce a carbonic acid solution that in turn is reacted on-site with limestone to form Ca2+ and HCO3-. This calcium bicarbonate solution is then released and diluted in the ocean where it would add minimally to the existing, large pool of these ions in the sea. Such a process simply speeds up natural carbonate weathering and dissolution which will otherwise consume anthropogenic CO2, but over many millennia. Using a schematic model of ocean chemistry and transport we show that this process would increase ocean alkalinity, effectively neutralizing CO2 acidity and isolating anthropogenic carbon from the atmosphere. Relative to atmospheric release or direct CO2 injection, this method would greatly expand the capacity of the ocean to store anthropogenic carbon while minimizing environmental impacts of this carbon on ocean biota. This technique also is less energy intensive and less expensive than other abiotic CO2 capture and sequestration schemes. We calculate an energy penalty that may be <2% with a CO2 capture efficiency which may exceed 50%. Estimated sequestration costs could be as low as \\12 per tonne CO_{2} sequestered, dependent on reactor configuration and on limestone and water availability and transport. These compare with \\90 to \\180/tonne CO_{2} and >>20% energy penalties estimated for direct ocean CO_{2}$ injection.

  5. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Raghubir P. Gupta; Douglas P. Harrison; Ya Liang

    2001-10-01

    The objective of this project is to develop a simple, inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable, sodium-based sorbent. The sorbent being used in this project is sodium carbonate which is converted to sodium bicarbonate, ''baking soda,'' through reaction with carbon dioxide and water vapor. Sodium bicarbonate is regenerated to sodium carbonate when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. Testing conducted previously confirmed that the reaction rate and achievable CO{sub 2} capacity of sodium carbonate decreased with increasing temperature, and that the global rate of reaction of sodium carbonate to sodium bicarbonate increased with an increase in both CO{sub 2} and H{sub 2}O concentrations. Energy balance calculations indicated that the rate of heat removal from the particle surface may determine the reaction rate for a particular particle system. This quarter, thermogravimetric analyses (TGA) were conducted which indicated that calcination of sodium bicarbonate at temperatures as high as 200 C did not cause a significant decrease in activity in subsequent carbonation testing. When sodium bicarbonate was subjected to a five cycle calcination/carbonation test, activity declined slightly over the first two cycles but was constant thereafter. TGA tests were also conducted with two other potential sorbents. Potassium carbonate was found to be less active than sodium carbonate, at conditions of interest in preliminary TGA tests. Sodium carbonate monohydrate showed negligible activity. Testing was also conducted in a 2-inch internal diameter quartz fluidized-bed reactor system. A five cycle test demonstrated that initial removals of 10 to 15 percent of the carbon dioxide in a simulated flue gas could be achieved. The carbonation reaction proceeded at temperatures as low as 41 C. Future work by TGA and in fixed-bed, fluidized-bed, and transport

  6. Moisture-swing sorption for carbon dioxide capture from ambient air: a thermodynamic analysis.

    PubMed

    Wang, Tao; Lackner, Klaus S; Wright, Allen B

    2013-01-14

    An ideal chemical sorbent for carbon dioxide capture from ambient air (air capture) must have a number of favourable properties, such as environmentally benign behaviour, a high affinity for CO(2) at very low concentration (400 ppm), and a low energy cost for regeneration. The last two properties seem contradictory, especially for sorbents employing thermal swing adsorption. On the other hand, thermodynamic analysis shows that the energy cost of an air capture device need only be slightly larger than that of a flue gas scrubber. The moisture swing separation process studied in this paper provides a novel approach to low cost CO(2) capture from air. The anionic exchange resin sorbent binds CO(2) when dry and releases it when wet. A thermodynamic model with coupled phase and chemical equilibria is developed to study the complex H(2)O-CO(2)-resin system. The moisture swing behaviour is compatible with hydration energies changing with the activity of water on the resin surfaces. This activity is in turn set by the humidity. The rearrangement of hydration water on the resin upon the sorption of a CO(2) molecule is predicted as a function of the humidity and temperature. Using water as fuel to drive the moisture swing enables an economical, large-scale implementation of air capture. By generating CO(2) with low partial pressures, the present technology has implications for in situ CO(2) utilizations which require low pressure CO(2) gas rather than liquid CO(2). PMID:23172123

  7. Process for removing sulfur dioxide from gas

    SciTech Connect

    Parish, W.R.

    1980-06-03

    There is disclosed a process for obtaining purer sodium sulfate from a mixture of solids containing sodium sulfate and sodium sulfite. The process involves contacting an aqueous slurry of the sulfate-sulfite mixture with a sulfur dioxide-containing gas under conditions which solubilize a significant amount of the sulfite as sodium bisulfite dissolved in the liquid aqueous phase. The remaining solid phase contains sodium sulfate of greater purity than in the mixture treated with sulfur dioxide. The mixture of sodium sulfate and sodium sulfite which is purified by the process may be obtained advantageously as a purge material from a process for removing sulfur dioxide from a gas stream.

  8. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Thomas Nelson; Raghubir P. Gupta

    2005-01-01

    This report describes research conducted between October 1, 2004 and December 31, 2004 on the use of dry regenerable sorbents for removal of carbon dioxide from flue gas. Two supported sorbents were tested in a bench scale fluidized bed reactor system. The sorbents were prepared by impregnation of sodium carbonate on to an inert support at a commercial catalyst manufacturing facility. One sorbent, tested through five cycles of carbon dioxide sorption in an atmosphere of 3% water vapor and 0.8 to 3% carbon dioxide showed consistent reactivity with sodium carbonate utilization of 7 to 14%. A second, similarly prepared material, showed comparable reactivity in one cycle of testing. Batches of 5 other materials were prepared in laboratory scale quantities (primarily by spray drying). These materials generally have significantly greater surface areas than calcined sodium bicarbonate. Small scale testing showed no significant adsorption of mercury on representative carbon dioxide sorbent materials under expected flue gas conditions.

  9. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Thomas Nelson; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta

    2005-04-01

    This report describes research conducted between January 1, 2005 and March 31, 2005 on the use of dry regenerable sorbents for removal of carbon dioxide from flue gas. Engineered sorbents composed of sodium carbonate on a ceramic support were tested in a laboratory fluidized bed reactor system and found to be capable of essentially complete removal of carbon dioxide at 60 C in a short residence time. Upon breakthrough the sorbents can be thermally regenerated to recover essentially all of the absorbed carbon dioxide. An optimized supported sorbent tested in a pilot-scale entrained bed absorber retained its reactivity in multicycle tests and experienced no attrition. Removal of >90% of carbon dioxide in simulated flue gas was achieved in an entrained bed reactor.

  10. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Ya Liang; Douglas P. Harrison

    2003-01-01

    The objective of this project is to develop a simple and inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable sorbent. The sorbents being investigated in this project are primarily alkali carbonates, and particularly sodium carbonate and potassium carbonate, which are converted to bicarbonates or intermediate salts through reaction with carbon dioxide and water vapor. Bicarbonates are regenerated to carbonates when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, electrobalance tests suggested that high calcination temperatures decrease the activity of sodium bicarbonate Grade 1 (SBC No.1) during subsequent carbonation cycles, but there is little or no progressive decrease in activity in successive cycles. SBC No.1 appears to be more active than SBC No.3. As expected, the presence of SO{sub 2} in simulated flue gas results in a progressive loss of sorbent capacity with increasing cycles. This is most likely due to an irreversible reaction to produce Na{sub 2}SO{sub 3}. This compound appears to be stable at calcination temperatures as high as 200 C. Tests of 40% supported potassium carbonate sorbent and plain support material suggest that some of the activity observed in tests of the supported sorbent may be due to adsorption by the support material rather than to carbonation of the sorbent.

  11. Carbon dioxide capturing technologies: a review focusing on metal organic framework materials (MOFs).

    PubMed

    Sabouni, Rana; Kazemian, Hossein; Rohani, Sohrab

    2014-04-01

    In this study, a relevant literature has been reviewed focusing on the carbon dioxide capture technologies in general, such as amine-based absorption as conventional carbon dioxide capturing technology, aqueous ammonia-based absorption, membranes, and adsorption material (e.g., zeolites, and activated carbons). In more details, metal organic frameworks (MOFs) as new emerging technologies for carbon dioxide adsorption are discussed. The MOFs section is intended to provide a comprehensive overview of MOFs including material characteristics and synthesis, structural features, CO2 adsorption capacity, heat of adsorption and selectivity of CO2. PMID:24338107

  12. Capturing carbon dioxide as a polymer from natural gas.

    PubMed

    Hwang, Chih-Chau; Tour, Josiah J; Kittrell, Carter; Espinal, Laura; Alemany, Lawrence B; Tour, James M

    2014-06-03

    Natural gas is considered the cleanest and recently the most abundant fossil fuel source, yet when it is extracted from wells, it often contains 10-20 mol% carbon dioxide (20-40 wt%), which is generally vented to the atmosphere. Efforts are underway to contain this carbon dioxide at the well-head using inexpensive and non-corrosive methods. Here we report nucleophilic porous carbons are synthesized from simple and inexpensive carbon-sulphur and carbon-nitrogen precursors. Infrared, Raman and (13)C nuclear magnetic resonance signatures substantiate carbon dioxide fixation by polymerization in the carbon channels to form poly(CO2) under much lower pressures than previously required. This growing chemisorbed sulphur- or nitrogen-atom-initiated poly(CO2) chain further displaces physisorbed hydrocarbon, providing a continuous carbon dioxide selectivity. Once returned to ambient conditions, the poly(CO2) spontaneously depolymerizes, leading to a sorbent that can be easily regenerated without the thermal energy input that is required for traditional sorbents.

  13. Capturing carbon dioxide as a polymer from natural gas

    NASA Astrophysics Data System (ADS)

    Hwang, Chih-Chau; Tour, Josiah J.; Kittrell, Carter; Espinal, Laura; Alemany, Lawrence B.; Tour, James M.

    2014-06-01

    Natural gas is considered the cleanest and recently the most abundant fossil fuel source, yet when it is extracted from wells, it often contains 10-20 mol% carbon dioxide (20-40 wt%), which is generally vented to the atmosphere. Efforts are underway to contain this carbon dioxide at the well-head using inexpensive and non-corrosive methods. Here we report nucleophilic porous carbons are synthesized from simple and inexpensive carbon-sulphur and carbon-nitrogen precursors. Infrared, Raman and 13C nuclear magnetic resonance signatures substantiate carbon dioxide fixation by polymerization in the carbon channels to form poly(CO2) under much lower pressures than previously required. This growing chemisorbed sulphur- or nitrogen-atom-initiated poly(CO2) chain further displaces physisorbed hydrocarbon, providing a continuous carbon dioxide selectivity. Once returned to ambient conditions, the poly(CO2) spontaneously depolymerizes, leading to a sorbent that can be easily regenerated without the thermal energy input that is required for traditional sorbents.

  14. Synergistic Carbon Dioxide Capture and Conversion in Porous Materials.

    PubMed

    Zhang, Yugen; Lim, Diane S W

    2015-08-24

    Global climate change and excessive CO2 emissions have caused widespread public concern in recent years. Tremendous efforts have been made towards CO2 capture and conversion. This has led to the development of numerous porous materials as CO2 capture sorbents. Concurrently, the conversion of CO2 into value-added products by chemical methods has also been well-documented recently. However, realizing the attractive prospect of direct, in situ chemical conversion of captured CO2 into other chemicals remains a challenge.

  15. Neutron capture in the r-process

    SciTech Connect

    Surman, Rebecca; Mclaughlin, Gail C; Mumpower, Matthew; Hix, William Raphael; Jones, K. L.

    2010-01-01

    Recently we have shown that neutron capture rates on nuclei near stability significantly influence the r-process abundance pattern. We discuss the different mechanisms by which the abundance pattern is sensitive to the capture rates and identify key nuclei whose rates are of particular im- portance. Here we consider nuclei in the A = 130 and A = 80 regions.

  16. Carbon dioxide capture from atmospheric air using sodium hydroxide spray.

    PubMed

    Stolaroff, Joshuah K; Keith, David W; Lowry, Gregory V

    2008-04-15

    In contrast to conventional carbon capture systems for power plants and other large point sources, the system described in this paper captures CO2 directly from ambient air. This has the advantages that emissions from diffuse sources and past emissions may be captured. The objective of this research is to determine the feasibility of a NaOH spray-based contactor for use in an air capture system by estimating the cost and energy requirements per unit CO2 captured. A prototype system is constructed and tested to measure CO2 absorption, energy use, and evaporative water loss and compared with theoretical predictions. A numerical model of drop collision and coalescence is used to estimate operating parameters for a full-scale system, and the cost of operating the system per unit CO2 captured is estimated. The analysis indicates that CO2 capture from air for climate change mitigation is technically feasible using off-the-shelf technology. Drop coalescence significantly decreases the CO2 absorption efficiency; however, fan and pump energy requirements are manageable. Water loss is significant (20 mol H2O/mol CO2 at 15 degrees C and 65% RH) but can be lowered by appropriately designing and operating the system. The cost of CO2 capture using NaOH spray (excluding solution recovery and CO2 sequestration, which may be comparable) in the full-scale system is 96 $/ton-CO2 in the base case, and ranges from 53 to 127 $/ton-CO2 under alternate operating parameters and assumptions regarding capital costs and mass transfer rate. The low end of the cost range is reached by a spray with 50 microm mean drop diameter, which is achievable with commercially available spray nozzles.

  17. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Raghubir P. Gupta; William J. McMichael; Douglas P. Harrison; Ya Liang

    2002-01-01

    The objective of this project is to develop a simple, inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable, sodium-based sorbent. The sorbent being used in this project is sodium carbonate which is converted to sodium bicarbonate, or ''baking soda,'' through reaction with carbon dioxide and water vapor. Sodium bicarbonate is regenerated to sodium carbonate when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, five cycle thermogravimetric tests were conducted at the Louisiana State University (LSU) with sodium bicarbonate Grade 3 (SBC{number_sign}3) which showed that carbonation activity declined slightly over 5 cycles following severe calcination conditions of 200 C in pure CO{sub 2}. Three different sets of calcination conditions were tested. Initial carbonation activity (as measured by extent of reaction in the first 25 minutes) was greatest subsequent to calcination at 120 C in He, slightly less subsequent to calcination in 80% CO{sub 2}/20% H{sub 2}O, and lowest subsequent to calcination in pure CO{sub 2} at 200 C. Differences in the extent of reaction after 150 minutes of carbonation, subsequent to calcination under the same conditions followed the same trend but were less significant. The differences between fractional carbonation under the three calcination conditions declined with increasing cycles. A preliminary fixed bed reactor test was also conducted at LSU. Following calcination, the sorbent removed approximately 19% of the CO{sub 2} in the simulated flue gas. CO{sub 2} evolved during subsequent calcination was consistent with an extent of carbonation of approximately 49%. Following successful testing of SBC{number_sign}3 sorbent at RTI reported in the last quarter, a two cycle fluidized bed reactor test was conducted with trona as the sorbent precursor, which was calcined to sodium carbonate. In the first carbonation cycle, CO

  18. Regenerable immobilized aminosilane sorbents for carbon dioxide capture applications

    SciTech Connect

    Gay, McMahan; Choi, Sunho; Jones, Christopher W

    2014-09-16

    A method for the separation of carbon dioxide from ambient air and flue gases is provided wherein a phase separating moiety with a second moiety are simultaneously coupled and bonded onto an inert substrate to create a mixture which is subsequently contacted with flue gases or ambient air. The phase-separating moiety is an amine whereas the second moiety is an aminosilane, or a Group 4 propoxide such as titanium (IV) propoxide (tetrapropyl orthotitanate, C.sub.12H.sub.28O.sub.4Ti). The second moiety makes the phase-separating moiety insoluble in the pores of the inert substrate. The new sorbents have a high carbon dioxide loading capacity and considerable stability over hundreds of cycles. The synthesis method is readily scalable for commercial and industrial production.

  19. Better Enzymes for Carbon Capture: Low-Cost Biological Catalyst to Enable Efficient Carbon Dioxide Capture

    SciTech Connect

    2010-07-01

    IMPACCT Project: Codexis is developing new and efficient forms of enzymes known as carbonic anhydrases to absorb CO2 more rapidly and under challenging conditions found in the gas exhaust of coal-fired power plants. Carbonic anhydrases are common and are among the fastest enzymes, but they are not robust enough to withstand the harsh environment found in the power plant exhaust steams. In this project, Codexis will be using proprietary technology to improve the enzymes’ ability to withstand high temperatures and large swings in chemical composition. The project aims to develop a carbon-capture process that uses less energy and less equipment than existing approaches. This would reduce the cost of retrofitting today’s coal-fired power plants.

  20. Reducing Greenhouse Gas Emissions with Carbon Dioxide Capture and Sequestration in Deep Geological Formations

    SciTech Connect

    Benson, Dr. Sally; Cole, David R

    2008-01-01

    Carbon dioxide capture and sequestration (CCS) in deep geological formations has quickly emerged as an important option for reducing greenhouse emissions. If CCS is implemented on the scale needed for large reductions in CO2 emissions, a billion of tonnes or more of CO2 will be sequestered annually a 250 fold increase over the amount sequestered annually today. Sequestering these large volumes will require a strong scientific foundation of the coupled hydrological-geochemical-geomechanical processes that govern the long term fate of CO2 in the subsurface. Methods to characterize and select sequestration sites, subsurface engineering to optimize performance and cost, safe operations, monitoring technology, remediation methods, regulatory oversight, and an institutional approach for managing long term liability are also needed.

  1. Generation, capture, and utilization of industrial carbon dioxide.

    PubMed

    Hunt, Andrew J; Sin, Emily H K; Marriott, Ray; Clark, James H

    2010-03-22

    As a carbon-based life form living in a predominantly carbon-based environment, it is not surprising that we have created a carbon-based consumer society. Our principle sources of energy are carbon-based (coal, oil, and gas) and many of our consumer goods are derived from organic (i.e., carbon-based) chemicals (including plastics, fabrics and materials, personal care and cleaning products, dyes, and coatings). Even our large-volume inorganic-chemicals-based industries, including fertilizers and construction materials, rely on the consumption of carbon, notably in the form of large amounts of energy. The environmental problems which we now face and of which we are becoming increasingly aware result from a human-induced disturbance in the natural carbon cycle of the Earth caused by transferring large quantities of terrestrial carbon (coal, oil, and gas) to the atmosphere, mostly in the form of carbon dioxide. Carbon is by no means the only element whose natural cycle we have disturbed: we are transferring significant quantities of elements including phosphorus, sulfur, copper, and platinum from natural sinks or ores built up over millions of years to unnatural fates in the form of what we refer to as waste or pollution. However, our complete dependence on the carbon cycle means that its disturbance deserves special attention, as is now manifest in indicators such as climate change and escalating public concern over global warming. As with all disturbances in materials balances, we can seek to alleviate the problem by (1) dematerialization: a reduction in consumption; (2) rematerialization: a change in what we consume; or (3) transmaterialization: changing our attitude towards resources and waste. The "low-carbon" mantra that is popularly cited by organizations ranging from nongovernmental organizations to multinational companies and from local authorities to national governments is based on a combination of (1) and (2) (reducing carbon consumption though greater

  2. Generation, capture, and utilization of industrial carbon dioxide.

    PubMed

    Hunt, Andrew J; Sin, Emily H K; Marriott, Ray; Clark, James H

    2010-03-22

    As a carbon-based life form living in a predominantly carbon-based environment, it is not surprising that we have created a carbon-based consumer society. Our principle sources of energy are carbon-based (coal, oil, and gas) and many of our consumer goods are derived from organic (i.e., carbon-based) chemicals (including plastics, fabrics and materials, personal care and cleaning products, dyes, and coatings). Even our large-volume inorganic-chemicals-based industries, including fertilizers and construction materials, rely on the consumption of carbon, notably in the form of large amounts of energy. The environmental problems which we now face and of which we are becoming increasingly aware result from a human-induced disturbance in the natural carbon cycle of the Earth caused by transferring large quantities of terrestrial carbon (coal, oil, and gas) to the atmosphere, mostly in the form of carbon dioxide. Carbon is by no means the only element whose natural cycle we have disturbed: we are transferring significant quantities of elements including phosphorus, sulfur, copper, and platinum from natural sinks or ores built up over millions of years to unnatural fates in the form of what we refer to as waste or pollution. However, our complete dependence on the carbon cycle means that its disturbance deserves special attention, as is now manifest in indicators such as climate change and escalating public concern over global warming. As with all disturbances in materials balances, we can seek to alleviate the problem by (1) dematerialization: a reduction in consumption; (2) rematerialization: a change in what we consume; or (3) transmaterialization: changing our attitude towards resources and waste. The "low-carbon" mantra that is popularly cited by organizations ranging from nongovernmental organizations to multinational companies and from local authorities to national governments is based on a combination of (1) and (2) (reducing carbon consumption though greater

  3. Carbon dioxide capture using polyethylenimine-loaded mesoporous carbons.

    PubMed

    Wang, Jitong; Chen, Huichao; Zhou, Huanhuan; Liu, Xiaojun; Qiao, Wenming; Long, Donghui; Ling, Licheng

    2013-01-01

    A high efficiency sorbent for CO2 capture was developed by loading polyethylenimine (PEI) on mesoporous carbons which possessed well-developed mesoporous structures and large pore volume. The physicochemical properties of the sorbent were characterized by N2 adsorption/desorption, scanning electron microscopy (SEM), thermal gravimetric analysis (TG) and Fourier transform infrared spectroscopy (FT-IR) techniques followed by testing for CO2 capture. Factors that affected the sorption capacity of the sorbent were studied. The sorbent exhibited extraordinary capture capacity with CO2 concentration ranging from 5% to 80%. The optimal PEI loading was determined to be 65 wt.% with a CO2 sorption capacity of 4.82 mmol-CO2/g-sorbent in 15% CO2/N2 at 75 degrees C, owing to low mass-transfer resistance and a high utilization ratio of the amine compound (63%). Moisture had a promoting effect on the sorption separation of CO2. In addition, the developed sorbent could be regenerated easily at 100 degrees C, and it exhibited excellent regenerability and stability. These results indicate that this PEI-loaded mesoporous carbon sorbent should have a good potential for CO2 capture in the future.

  4. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Thomas Nelson

    2004-04-01

    This report describes research conducted between January 1, 2004 and March 31, 2004 on the use of dry regenerable sorbents for removal of carbon dioxide from flue gas. RTI has produced laboratory scale batches (approximately 300 grams) of supported sorbents (composed of 20 to 40% sodium carbonate) with high surface area and acceptable activity. Initial rates of weight gain of the supported sorbents when exposed to a simulated flue gas exceeded that of 100% calcined sodium bicarbonate. One of these sorbents was tested through six cycles of carbonation/calcination by thermogravimetric analysis and found to have consistent carbonation activity. Kinetic modeling of the regeneration cycle on the basis of diffusion resistance at the particle surface is impractical, because the evolving gases have an identical composition to those assumed for the bulk fluidization gas. A kinetic model of the reaction has been developed on the basis of bulk motion of water and carbon dioxide at the particle surface (as opposed to control by gas diffusion). The model will be used to define the operating conditions in future laboratory- and pilot-scale testing.

  5. Carbon Dioxide Capture from Flue Gas Using Dry, Regenerable Sorbents

    SciTech Connect

    David A. Green; Thomas O. Nelson; Brian S. Turk; Paul D. Box; Andreas Weber; Raghubir P. Gupta

    2006-01-01

    This report describes research conducted between October 1, 2005, and December 31, 2005, on the use of dry regenerable sorbents for removal of carbon dioxide (CO{sub 2}) from flue gas from coal combustion. A field test was conducted to examine the extent to which RTI's supported sorbent can be regenerated in a heated, hollow screw conveyor. This field test was conducted at the facilities of a screw conveyor manufacturer. The sorbent was essentially completely regenerated during this test, as confirmed by thermal desorption and mass spectroscopy analysis of the regenerated sorbent. Little or no sorbent attrition was observed during 24 passes through the heated screw conveyor system. Three downflow contactor absorption tests were conducted using calcined sodium bicarbonate as the absorbent. Maximum carbon dioxide removals of 57 and 91% from simulated flue gas were observed at near ambient temperatures with water-saturated gas. These tests demonstrated that calcined sodium carbonate is not as effective at removing CO{sub 2} as are supported sorbents containing 10 to 15% sodium carbonate. Delivery of the hollow screw conveyor for the laboratory-scale sorbent regeneration system was delayed; however, construction of other components of this system continued during the quarter.

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

    SciTech Connect

    Lin, Jerry

    2014-09-30

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

  7. Water surface capturing by image processing

    Technology Transfer Automated Retrieval System (TEKTRAN)

    An alternative means of measuring the water surface interface during laboratory experiments is processing a series of sequentially captured images. Image processing can provide a continuous, non-intrusive record of the water surface profile whose accuracy is not dependent on water depth. More trad...

  8. An investigation of carbon dioxide capture by chitin acetate/DMSO binary system.

    PubMed

    Eftaiha, Ala'a F; Alsoubani, Fatima; Assaf, Khaleel I; Troll, Carsten; Rieger, Bernhard; Khaled, Aseel H; Qaroush, Abdussalam K

    2016-11-01

    Chitin is considered to be the second most abundant naturally-occurring polysaccharide. Also, dimethyl sulfoxide (DMSO) is the second highest dielectric constant polar solvent after water. Despite the low solubility of chitin in common organic solvents, and due to its high nitrogen content, it may serve as a potential scrubbing agent "wet scrubbing" for carbon dioxide (CO2) capturing as an alternative to monoethanolamine "renewables for renewables approach". Briefly, a detailed investigation for the utilization of low molecular weight, chitin-acetate (CA) in DMSO for the capturing of CO2 is reported. As carbonation process takes place, the formation of ionic alkylcarbonate was confirmed throughout spectroscopic and computational studies. Supramolecular chemisorption was proven throughout (1)H Nuclear Magnetic Resonance ((1)H NMR) together with the absence of sorption of CO2 by the monomeric repeating unit, glucosamine hydrochloride. Further, Density Functional Theory (DFT) calculations supported the formation of the CA/CO2 adduct through a newly formed supramolecular ionic interaction and hydrogen bonding along the oligosaccharide backbone between the neighboring ammonium ion and hydroxyl functional groups. The sorption capacity was measured volumetrically within an in situ Attenuated Total Reflectance-Fourier Transform Infrared coupled (in situ ATR-FTIR) autoclave at 25.0°C, and 4.0bar CO2, with a maximum sorption capacity of 3.63 [Formula: see text] /gsorbent at 10.0% (w/v). PMID:27516261

  9. An investigation of carbon dioxide capture by chitin acetate/DMSO binary system.

    PubMed

    Eftaiha, Ala'a F; Alsoubani, Fatima; Assaf, Khaleel I; Troll, Carsten; Rieger, Bernhard; Khaled, Aseel H; Qaroush, Abdussalam K

    2016-11-01

    Chitin is considered to be the second most abundant naturally-occurring polysaccharide. Also, dimethyl sulfoxide (DMSO) is the second highest dielectric constant polar solvent after water. Despite the low solubility of chitin in common organic solvents, and due to its high nitrogen content, it may serve as a potential scrubbing agent "wet scrubbing" for carbon dioxide (CO2) capturing as an alternative to monoethanolamine "renewables for renewables approach". Briefly, a detailed investigation for the utilization of low molecular weight, chitin-acetate (CA) in DMSO for the capturing of CO2 is reported. As carbonation process takes place, the formation of ionic alkylcarbonate was confirmed throughout spectroscopic and computational studies. Supramolecular chemisorption was proven throughout (1)H Nuclear Magnetic Resonance ((1)H NMR) together with the absence of sorption of CO2 by the monomeric repeating unit, glucosamine hydrochloride. Further, Density Functional Theory (DFT) calculations supported the formation of the CA/CO2 adduct through a newly formed supramolecular ionic interaction and hydrogen bonding along the oligosaccharide backbone between the neighboring ammonium ion and hydroxyl functional groups. The sorption capacity was measured volumetrically within an in situ Attenuated Total Reflectance-Fourier Transform Infrared coupled (in situ ATR-FTIR) autoclave at 25.0°C, and 4.0bar CO2, with a maximum sorption capacity of 3.63 [Formula: see text] /gsorbent at 10.0% (w/v).

  10. Molecular Simulation of Carbon Dioxide Capture by Montmorillonite Using an Accurate and Flexible Force Field

    SciTech Connect

    Romanov, V N; Cygan, R T; Myshakin, E M

    2012-06-21

    Naturally occurring clay minerals provide a distinctive material for carbon capture and carbon dioxide sequestration. Swelling clay minerals, such as the smectite variety, possess an aluminosilicate structure that is controlled by low-charge layers that readily expand to accommodate water molecules and, potentially, CO2. Recent experimental studies have demonstrated the efficacy of intercalating CO2 in the interlayer of layered clays, but little is known about the molecular mechanisms of the process and the extent of carbon capture as a function of clay charge and structure. A series of molecular dynamics simulations and vibrational analyses have been completed to assess the molecular interactions associated with incorporation of CO2 and H2O in the interlayer of montmorillonite clay and to help validate the models with experimental observation. An accurate and fully flexible set of interatomic potentials for CO2 is developed and combined with Clayff potentials to help evaluate the intercalation mechanism and examine the effect of molecular flexibility onthe diffusion rate of CO2 in water.

  11. Yeast-based microporous carbon materials for carbon dioxide capture.

    PubMed

    Shen, Wenzhong; He, Yue; Zhang, Shouchun; Li, Junfen; Fan, Weibin

    2012-07-01

    A hierarchical microporous carbon material with a Brunauer-Emmett-Teller surface area of 1348 m(2) g(-1) and a pore volume of 0.67 cm(3) g(-1) was prepared from yeast through chemical activation with potassium hydroxide. This type of material contains large numbers of nitrogen-containing groups (nitrogen content >5.3 wt%), and, consequently, basic sites. As a result, this material shows a faster adsorption rate and a higher adsorption capacity of CO(2) than the material obtained by directly carbonizing yeast under the same conditions. The difference is more pronounced in the presence of N(2) or H(2)O, showing that chemical activation of discarded yeast with potassium hydroxide could afford high-performance microporous carbon materials for the capture of CO(2).

  12. Technologies to reduce or capture and store carbon dioxide emissions

    SciTech Connect

    Nelson, G.; Mueller, M.; McCall, M.; Knipp, R.

    2007-06-15

    The report focuses on a broad suite of technologies to reduce, capture and store CO{sub 2} emissions, primarily as they relate to direct coal combustion and also coal gasification and liquefaction. The report surveys and summarizes existing research, discusses relevant federal programs, makes recommendations regarding additional research opportunities and public policy objectives, and recommends a technology-based framework for mitigating CO{sub 2} emissions from coal-based electricity generation plants. The US Department of Energy is already at work to foster the development of these technologies. The report recognizes the scope of that work and in essence, concludes that much work still remains. A summary of the report is published in hard copy and on the CD-ROM. The full 160 page report is on the CD-ROM.

  13. Synthesis of optimal adsorptive carbon capture processes.

    SciTech Connect

    chang, Y.; Cozad, A.; Kim, H.; Lee, A.; Vouzis, P.; Konda, M.; Simon, A.; Sahinidis, N.; Miller, D.

    2011-01-01

    Solid sorbent carbon capture systems have the potential to require significantly lower regeneration energy compared to aqueous monoethanol amine (MEA) systems. To date, the majority of work on solid sorbents has focused on developing the sorbent materials themselves. In order to advance these technologies, it is necessary to design systems that can exploit the full potential and unique characteristics of these materials. The Department of Energy (DOE) recently initiated the Carbon Capture Simulation Initiative (CCSI) to develop computational tools to accelerate the commercialization of carbon capture technology. Solid sorbents is the first Industry Challenge Problem considered under this initiative. An early goal of the initiative is to demonstrate a superstructure-based framework to synthesize an optimal solid sorbent carbon capture process. For a given solid sorbent, there are a number of potential reactors and reactor configurations consisting of various fluidized bed reactors, moving bed reactors, and fixed bed reactors. Detailed process models for these reactors have been modeled using Aspen Custom Modeler; however, such models are computationally intractable for large optimization-based process synthesis. Thus, in order to facilitate the use of these models for process synthesis, we have developed an approach for generating simple algebraic surrogate models that can be used in an optimization formulation. This presentation will describe the superstructure formulation which uses these surrogate models to choose among various process alternatives and will describe the resulting optimal process configuration.

  14. Synthesis and characterization of functional thienyl-phosphine microporous polymers for carbon dioxide capture.

    PubMed

    Chen, Xianghui; Qiao, Shanlin; Du, Zhengkun; Zhou, Yuanhang; Yang, Renqiang

    2013-07-25

    A novel kind of functional organic microporous polymer is designed by introducing polar organic groups (P=O and P=S) and electron-rich heterocyclic into the framework to obtain high carbon dioxide capture capacity. The estimated Brunauer-Emmett-Teller (BET) surface areas of these polymers are about 600 m(2) g(-1) and the highest CO2 uptake is 2.26 mmol g(-1) (1.0 bar/273 K). Interestingly, the polymer containing P=O groups shows greater CO2 capture capacity than that containing P=S groups at the same temperature. In addition, these polymers show high isosteric heats of CO2 adsorption (28.6 kJ mol(-1) ), which can be competitive with some nitrogen-rich networks. Therefore, these microporous polymers are promising candidates for carbon dioxide capture.

  15. Asphalt-derived high surface area activated porous carbons for carbon dioxide capture.

    PubMed

    Jalilov, Almaz S; Ruan, Gedeng; Hwang, Chih-Chau; Schipper, Desmond E; Tour, Josiah J; Li, Yilun; Fei, Huilong; Samuel, Errol L G; Tour, James M

    2015-01-21

    Research activity toward the development of new sorbents for carbon dioxide (CO2) capture have been increasing quickly. Despite the variety of existing materials with high surface areas and high CO2 uptake performances, the cost of the materials remains a dominant factor in slowing their industrial applications. Here we report preparation and CO2 uptake performance of microporous carbon materials synthesized from asphalt, a very inexpensive carbon source. Carbonization of asphalt with potassium hydroxide (KOH) at high temperatures (>600 °C) yields porous carbon materials (A-PC) with high surface areas of up to 2780 m(2) g(-1) and high CO2 uptake performance of 21 mmol g(-1) or 93 wt % at 30 bar and 25 °C. Furthermore, nitrogen doping and reduction with hydrogen yields active N-doped materials (A-NPC and A-rNPC) containing up to 9.3% nitrogen, making them nucleophilic porous carbons with further increase in the Brunauer-Emmett-Teller (BET) surface areas up to 2860 m(2) g(-1) for A-NPC and CO2 uptake to 26 mmol g(-1) or 114 wt % at 30 bar and 25 °C for A-rNPC. This is the highest reported CO2 uptake among the family of the activated porous carbonaceous materials. Thus, the porous carbon materials from asphalt have excellent properties for reversibly capturing CO2 at the well-head during the extraction of natural gas, a naturally occurring high pressure source of CO2. Through a pressure swing sorption process, when the asphalt-derived material is returned to 1 bar, the CO2 is released, thereby rendering a reversible capture medium that is highly efficient yet very inexpensive.

  16. Thermodynamic analysis of low-temperature carbon dioxide and sulfur dioxide capture from coal-burning power plants.

    PubMed

    Swanson, Charles E; Elzey, John W; Hershberger, Robert E; Donnelly, Russell J; Pfotenhauer, John

    2012-07-01

    We discuss the possibility of capturing carbon dioxide from the flue gas of a coal-fired electrical power plant by cryogenically desublimating the carbon dioxide and then preparing it for transport in a pipeline to a sequestration site. Various other means have been proposed to accomplish the same goal. The problem discussed here is to estimate the "energy penalty" or "parasitic energy loss,' defined as the fraction of electrical output that will be needed to provide the refrigeration and that will then not be deliverable. We compute the energy loss (7.9-9.2% at 1 atm) based on perfect Carnot efficiency and estimate the achievable parasitic energy loss (22-26% at 1 atm) by incorporating the published coefficient of performance values for appropriately sized refrigeration or liquefaction cycles at the relevant temperatures. The analyses at 1 atm represent a starting point for future analyses using elevated pressures.

  17. CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS

    SciTech Connect

    David A. Green; Brian S. Turk; Raghubir Gupta; Alejandro Lopez-Ortiz

    2001-01-01

    Four grades of sodium bicarbonate and two grades of trona were characterized in terms of particle size distribution, surface area, pore size distribution, and attrition. Surface area and pore size distribution determinations were conducted after calcination of the materials. The sorbent materials were subjected to thermogravimetric testing to determine comparative rates and extent of calcination (in inert gas) and sorption (in a simulated coal combustion flue gas mixture). Selected materials were exposed to five calcination/sorption cycles and showed no decrease in either sorption capacity or sorption rate. Process simulations were conducted involving different heat recovery schemes. The process is thermodynamically feasible. The sodium-based materials appear to have suitable physical properties for use as regenerable sorbents and, based on thermogravimetric testing, are likely to have sorption and calcination rates that are rapid enough to be of interest in full-scale carbon sequestration processes.

  18. Bench Scale Thin Film Composite Hollow Fiber Membranes for Post-Combustion Carbon Dioxide Capture

    SciTech Connect

    Glaser, Paul; Bhandari, Dhaval; Narang, Kristi; McCloskey, Pat; Singh, Surinder; Ananthasayanam, Balajee; Howson, Paul; Lee, Julia; Wroczynski, Ron; Stewart, Frederick; Orme, Christopher; Klaehn, John; McNally, Joshua; Rownaghi, Ali; Lu, Liu; Koros, William; Goizueta, Roberto; Sethi, Vijay

    2015-04-01

    GE Global Research, Idaho National Laboratory (INL), Georgia Institute of Technology (Georgia Tech), and Western Research Institute (WRI) proposed to develop high performance thin film polymer composite hollow fiber membranes and advanced processes for economical post-combustion carbon dioxide (CO2) capture from pulverized coal flue gas at temperatures typical of existing flue gas cleanup processes. The project sought to develop and then optimize new gas separations membrane systems at the bench scale, including tuning the properties of a novel polyphosphazene polymer in a coating solution and fabricating highly engineered porous hollow fiber supports. The project also sought to define the processes needed to coat the fiber support to manufacture composite hollow fiber membranes with high performance, ultra-thin separation layers. Physical, chemical, and mechanical stability of the materials (individual and composite) towards coal flue gas components was considered via exposure and performance tests. Preliminary design, technoeconomic, and economic feasibility analyses were conducted to evaluate the overall performance and impact of the process on the cost of electricity (COE) for a coal-fired plant including capture technologies. At the onset of the project, Membranes based on coupling a novel selective material polyphosphazene with an engineered hollow fiber support was found to have the potential to capture greater than 90% of the CO2 in flue gas with less than 35% increase in COE, which would achieve the DOE-targeted performance criteria. While lab-scale results for the polyphosphazene materials were very promising, and the material was incorporated into hollow-fiber modules, difficulties were encountered relating to the performance of these membrane systems over time. Performance, as measured by both flux of and selectivity for CO2 over other flue gas constituents was found to deteriorate over time, suggesting a system that was

  19. Two-Dimensional Covalent Organic Frameworks for Carbon Dioxide Capture through Channel-Wall Functionalization

    PubMed Central

    Huang, Ning; Chen, Xiong; Krishna, Rajamani; Jiang, Donglin

    2015-01-01

    Ordered open channels found in two-dimensional covalent organic frameworks (2D COFs) could enable them to adsorb carbon dioxide. However, the frameworks’ dense layer architecture results in low porosity that has thus far restricted their potential for carbon dioxide adsorption. Here we report a strategy for converting a conventional 2D COF into an outstanding platform for carbon dioxide capture through channel-wall functionalization. The dense layer structure enables the dense integration of functional groups on the channel walls, creating a new version of COFs with high capacity, reusability, selectivity, and separation productivity for flue gas. These results suggest that channel-wall functional engineering could be a facile and powerful strategy to develop 2D COFs for high-performance gas storage and separation. PMID:25613010

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

    NASA Astrophysics Data System (ADS)

    Chaban, Vitaly

    2015-01-01

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

  1. TARGET: Rapid Capture of Process Knowledge

    NASA Technical Reports Server (NTRS)

    Ortiz, C. J.; Ly, H. V.; Saito, T.; Loftin, R. B.

    1993-01-01

    TARGET (Task Analysis/Rule Generation Tool) represents a new breed of tool that blends graphical process flow modeling capabilities with the function of a top-down reporting facility. Since NASA personnel frequently perform tasks that are primarily procedural in nature, TARGET models mission or task procedures and generates hierarchical reports as part of the process capture and analysis effort. Historically, capturing knowledge has proven to be one of the greatest barriers to the development of intelligent systems. Current practice generally requires lengthy interactions between the expert whose knowledge is to be captured and the knowledge engineer whose responsibility is to acquire and represent the expert's knowledge in a useful form. Although much research has been devoted to the development of methodologies and computer software to aid in the capture and representation of some types of knowledge, procedural knowledge has received relatively little attention. In essence, TARGET is one of the first tools of its kind, commercial or institutional, that is designed to support this type of knowledge capture undertaking. This paper will describe the design and development of TARGET for the acquisition and representation of procedural knowledge. The strategies employed by TARGET to support use by knowledge engineers, subject matter experts, programmers and managers will be discussed. This discussion includes the method by which the tool employs its graphical user interface to generate a task hierarchy report. Next, the approach to generate production rules for incorporation in and development of a CLIPS based expert system will be elaborated. TARGET also permits experts to visually describe procedural tasks as a common medium for knowledge refinement by the expert community and knowledge engineer making knowledge consensus possible. The paper briefly touches on the verification and validation issues facing the CLIPS rule generation aspects of TARGET. A description of

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

    PubMed Central

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

    2014-01-01

    Direct air capture is regarded as a plausible alternate approach that, if economically practical, can mitigate the increasing carbon dioxide emissions associated with two of the main carbon polluting sources, namely stationary power plants and transportation. Here we show that metal-organic framework crystal chemistry permits the construction of an isostructural metal-organic framework (SIFSIX-3-Cu) based on pyrazine/copper(II) two-dimensional periodic 44 square grids pillared by silicon hexafluoride anions and thus allows further contraction of the pore system to 3.5 versus 3.84 Å for the parent zinc(II) derivative. This enhances the adsorption energetics and subsequently displays carbon dioxide uptake and selectivity at very low partial pressures relevant to air capture and trace carbon dioxide removal. The resultant SIFSIX-3-Cu exhibits uniformly distributed adsorption energetics and offers enhanced carbon dioxide physical adsorption properties, uptake and selectivity in highly diluted gas streams, a performance, to the best of our knowledge, unachievable with other classes of porous materials. PMID:24964404

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

    PubMed

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

    2014-06-25

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

  4. Does Involuntary Attentional Capture Curtail Stimulus Processing

    NASA Technical Reports Server (NTRS)

    Remington, Roger W.; McLean, John P.; Folk, Charles L.; Null, Cynthia H. (Technical Monitor)

    1996-01-01

    Under certain conditions uninformative visual cues at non-target locations increase target RTs. The typical explanation is that visual attention has been involuntarily summoned to the cued location and is unavailable when needed at the target location. Here we present evidence that capture has not just oriented attention away from the target location, but has lead to the processing of stimuli at the location of the uninformative cue.

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

    DOEpatents

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

    2014-07-08

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

  6. Simteche Hydrate CO2 Capture Process

    SciTech Connect

    Nexant and Los Alamos National Laboratory

    2006-09-30

    As a result of an August 4, 2005 project review meeting held at Los Alamos National Laboratory (LANL) to assess the project's technical progress, Nexant/Simteche/LANL project team was asked to meet four targets related to the existing project efforts. The four targets were to be accomplished by the September 30, 2006. These four targets were: (1) The CO{sub 2} hydrate process needs to show, through engineering and sensitivity analysis, that it can achieve 90% CO{sub 2} capture from the treated syngas stream, operating at 1000 psia. The cost should indicate the potential of achieving the Sequestration Program's cost target of less than 10% increase in the cost of electricity (COE) of the non-CO{sub 2} removal IGCC plant or demonstrate a significant cost reduction from the Selexol process cost developed in the Phase II engineering analysis. (2) The ability to meet the 20% cost share requirement for research level efforts. (3) LANL identifies through equilibrium and bench scale testing a once-through 90% CO{sub 2} capture promoter that supports the potential to achieve the Sequestration Program's cost target. Nexant is to perform an engineering analysis case to verify any economic benefits, as needed; no ETM validation is required, however, for this promoter for FY06. (4) The CO{sub 2} hydrate once-through process is to be validated at 1000 psia with the ETM at a CO{sub 2} capture rate of 60% without H{sub 2}S. The performance of 68% rate of capture is based on a batch, equilibrium data with H{sub 2}S. Validation of the test results is required through multiple runs and engineering calculations. Operational issues will be solved that will specifically effect the validation of the technology. Nexant was given the primary responsibility for Target No.1, while Simteche was mainly responsible for Target No.2; with LANL having the responsibility of Targets No.3 and No.4.

  7. Carbon dioxide reduction by the Bosch process

    NASA Technical Reports Server (NTRS)

    Manning, M. P.; Reid, R. C.

    1975-01-01

    Prototype units for carrying out the reduction of carbon dioxide to elementary carbon have been built and operated successfully. In some cases, however, startup difficulties have been reported. Moreover, the recycle reactor product has been reported to contain only small amounts of water and undesirably high yields of methane. This paper presents the results of the first phase of an experimental study that was carried out to define the mechanisms occurring in the reduction process. Conclusions are drawn and possible modifications to the present recycle process are suggested.

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

    DOEpatents

    Wijmans, Johannes G.; Merkel, Timothy C; Baker, Richard W.

    2011-10-11

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

  9. Energy and economic analysis of the carbon dioxide capture installation with the use of monoethanolamine and ammonia

    NASA Astrophysics Data System (ADS)

    Bochon, Krzysztof; Chmielniak, Tadeusz

    2015-03-01

    In the study an accurate energy and economic analysis of the carbon capture installation was carried out. Chemical absorption with the use of monoethanolamine (MEA) and ammonia was adopted as the technology of carbon dioxide (CO2) capture from flue gases. The energy analysis was performed using a commercial software package to analyze the chemical processes. In the case of MEA, the demand for regeneration heat was about 3.5 MJ/kg of CO2, whereas for ammonia it totalled 2 MJ/kg CO2. The economic analysis was based on the net present value (NPV) method. The limit price for CO2 emissions allowances at which the investment project becomes profitable (NPV = 0) was more than 160 PLN/Mg for MEA and less than 150 PLN/Mg for ammonia. A sensitivity analysis was also carried out to determine the limit price of CO2 emissions allowances depending on electricity generation costs at different values of investment expenditures.

  10. Carbon dioxide capture strategies from flue gas using microalgae: a review.

    PubMed

    Thomas, Daniya M; Mechery, Jerry; Paulose, Sylas V

    2016-09-01

    Global warming and pollution are the twin crises experienced globally. Biological offset of these crises are gaining importance because of its zero waste production and the ability of the organisms to thrive under extreme or polluted condition. In this context, this review highlights the recent developments in carbon dioxide (CO2) capture from flue gas using microalgae and finding the best microalgal remediation strategy through contrast and comparison of different strategies. Different flue gas microalgal remediation strategies discussed are as follows: (i) Flue gas to CO2 gas segregation using adsorbents for microalgal mitigation, (ii) CO2 separation from flue gas using absorbents and later regeneration for microalgal mitigation, (iii) Flue gas to liquid conversion for direct microalgal mitigation, and (iv) direct flue gas mitigation using microalgae. This work also studies the economic feasibility of microalgal production. The study discloses that the direct convening of flue gas with high carbon dioxide content, into microalgal system is cost-effective.

  11. Carbon dioxide capture strategies from flue gas using microalgae: a review.

    PubMed

    Thomas, Daniya M; Mechery, Jerry; Paulose, Sylas V

    2016-09-01

    Global warming and pollution are the twin crises experienced globally. Biological offset of these crises are gaining importance because of its zero waste production and the ability of the organisms to thrive under extreme or polluted condition. In this context, this review highlights the recent developments in carbon dioxide (CO2) capture from flue gas using microalgae and finding the best microalgal remediation strategy through contrast and comparison of different strategies. Different flue gas microalgal remediation strategies discussed are as follows: (i) Flue gas to CO2 gas segregation using adsorbents for microalgal mitigation, (ii) CO2 separation from flue gas using absorbents and later regeneration for microalgal mitigation, (iii) Flue gas to liquid conversion for direct microalgal mitigation, and (iv) direct flue gas mitigation using microalgae. This work also studies the economic feasibility of microalgal production. The study discloses that the direct convening of flue gas with high carbon dioxide content, into microalgal system is cost-effective. PMID:27397026

  12. Mechanism Study of Carbon Dioxide Capture from Ambient Air by Hydration Energy Variation

    NASA Astrophysics Data System (ADS)

    Shi, X.; Lackner, K. S.

    2014-12-01

    Hydration of neutral and ionic species on solid interfaces plays an important role in a wide range of natural and engineered processes within energy systems as well as biological and environmental systems. Various chemical reactions are significantly enhanced, both in the rate and the extent of the reaction, because of water molecules present or absent at the interface. A novel technology for carbon dioxide capture, driven by the free energy difference between more or less hydrated states of an anionic exchange resin is studied for a new approach to absorb CO2 from ambient air. For these materials the affinity to CO2 is dramatically lowered as the availability of water is increased. This makes it possible to absorb CO2 from air in a dry environment and release it at two orders of magnitude larger partial pressures in a wet environment. While the absorption process and the thermodynamic properties of air capture via ion exchange resins have been demonstrated, the underlying physical mechanisms remain to be understood. In order to rationally design better sorbent materials, the present work elucidates through molecular dynamics and quantum mechanical modeling the energy changes in the carbonate, bicarbonate and hydroxide ions that are induced by hydration, and how these changes affect sorbent properties. A methodology is developed to determine the free energy change during carbonate ion hydrolysis changes with different numbers of water molecules present. This makes it possible to calculate the equilibrium in the reaction CO3--•nH2O ↔ HCO3- • m1H2O + OH- • m2H2O + (n - 1 - m1 - m2)H2O Molecular dynamics models are used to calculate free energies of hydration for the CO32- ion, the HCO3- ion, and the OH- ion as function of the amount of water that is present. A quantum mechanical model is employed to study the equilibrium of the reaction Na2CO3 + H2O ↔ NaHCO3 + NaOHin a vacuum and at room temperature. The computational analysis of the free energy of

  13. Carbon dioxide postcombustion capture: a novel screening study of the carbon dioxide absorption performance of 76 amines.

    PubMed

    Puxty, Graeme; Rowland, Robert; Allport, Andrew; Yang, Qi; Bown, Mark; Burns, Robert; Maeder, Marcel; Attalla, Moetaz

    2009-08-15

    The significant and rapid reduction of greenhouse gas emissions is recognized as necessary to mitigate the potential climate effects from global warming. The postcombustion capture (PCC) and storage of carbon dioxide (CO2) produced from the use of fossil fuels for electricity generation is a key technology needed to achieve these reductions. The most mature technology for CO2 capture is reversible chemical absorption into an aqueous amine solution. In this study the results from measurements of the CO2 absorption capacity of aqueous amine solutions for 76 different amines are presented. Measurements were made using both a novel isothermal gravimetric analysis (IGA) method and a traditional absorption apparatus. Seven amines, consisting of one primary, three secondary, and three tertiary amines, were identified as exhibiting outstanding absorption capacities. Most have a number of structural features in common including steric hindrance and hydroxyl functionality 2 or 3 carbons from the nitrogen. Initial CO2 absorption rate data from the IGA measurements was also used to indicate relative absorption rates. Most of the outstanding performers in terms of capacity also showed initial absorption rates comparable to the industry standard monoethanolamine (MEA). This indicates, in terms of both absorption capacity and kinetics, that they are promising candidates for further investigation.

  14. Automated full matrix capture for industrial processes

    NASA Astrophysics Data System (ADS)

    Brown, Roy H.; Pierce, S. Gareth; Collison, Ian; Dutton, Ben; Dziewierz, Jerzy; Jackson, Joseph; Lardner, Timothy; MacLeod, Charles; Morozov, Maxim

    2015-03-01

    Full matrix capture (FMC) ultrasound can be used to generate a permanent re-focusable record of data describing the geometry of a part; a valuable asset for an inspection process. FMC is a desirable acquisition mode for automated scanning of complex geometries, as it allows compensation for surface shape in post processing and application of the total focusing method. However, automating the delivery of such FMC inspection remains a significant challenge for real industrial processes due to the high data overhead associated with the ultrasonic acquisition. The benefits of NDE delivery using six-axis industrial robots are well versed when considering complex inspection geometries, but such an approach brings additional challenges to scanning speed and positional accuracy when combined with FMC inspection. This study outlines steps taken to optimize the scanning speed and data management of a process to scan the diffusion bonded membrane of a titanium test plate. A system combining a KUKA robotic arm and a reconfigurable FMC phased array controller is presented. The speed and data implications of different scanning methods are compared, and the impacts on data visualization quality are discussed with reference to this study. For the 0.5 m2 sample considered, typical acquisitions of 18 TB/m2 were measured for a triple back wall FMC acquisition, illustrating the challenge of combining high data throughput with acceptable scanning speeds.

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

    PubMed Central

    Minic, Zoran; Thongbam, Premila D.

    2011-01-01

    Deep sea hydrothermal vents are located along the mid-ocean ridge system, near volcanically active areas, where tectonic plates are moving away from each other. Sea water penetrates the fissures of the volcanic bed and is heated by magma. This heated sea water rises to the surface dissolving large amounts of minerals which provide a source of energy and nutrients to chemoautotrophic organisms. Although this environment is characterized by extreme conditions (high temperature, high pressure, chemical toxicity, acidic pH and absence of photosynthesis) a diversity of microorganisms and many animal species are specially adapted to this hostile environment. These organisms have developed a very efficient metabolism for the assimilation of inorganic CO2 from the external environment. In order to develop technology for the capture of carbon dioxide to reduce greenhouse gases in the atmosphere, enzymes involved in CO2 fixation and assimilation might be very useful. This review describes some current research concerning CO2 fixation and assimilation in the deep sea environment and possible biotechnological application of enzymes for carbon dioxide capture. PMID:21673885

  16. The biological deep sea hydrothermal vent as a model to study carbon dioxide capturing enzymes.

    PubMed

    Minic, Zoran; Thongbam, Premila D

    2011-01-01

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

  17. The biological deep sea hydrothermal vent as a model to study carbon dioxide capturing enzymes.

    PubMed

    Minic, Zoran; Thongbam, Premila D

    2011-01-01

    Deep sea hydrothermal vents are located along the mid-ocean ridge system, near volcanically active areas, where tectonic plates are moving away from each other. Sea water penetrates the fissures of the volcanic bed and is heated by magma. This heated sea water rises to the surface dissolving large amounts of minerals which provide a source of energy and nutrients to chemoautotrophic organisms. Although this environment is characterized by extreme conditions (high temperature, high pressure, chemical toxicity, acidic pH and absence of photosynthesis) a diversity of microorganisms and many animal species are specially adapted to this hostile environment. These organisms have developed a very efficient metabolism for the assimilation of inorganic CO₂ from the external environment. In order to develop technology for the capture of carbon dioxide to reduce greenhouse gases in the atmosphere, enzymes involved in CO₂ fixation and assimilation might be very useful. This review describes some current research concerning CO₂ fixation and assimilation in the deep sea environment and possible biotechnological application of enzymes for carbon dioxide capture. PMID:21673885

  18. A Novel System for Carbon Dioxide Capture Utilizing Electrochemical Membrane Technology

    SciTech Connect

    Ghezel-Ayagh, Hossein; Jolly, Stephen; Patel, Dilip; Hunt, Jennifer; Steen, William A.; Richardson, Carl F.; Marina, Olga A.

    2013-06-03

    FuelCell Energy, Inc. (FCE), in collaboration with Pacific Northwest National Laboratory (PNNL) and URS Corporation, is developing a novel Combined Electric Power and Carbon-Dioxide Separation (CEPACS) system, under a contract from the U.S. Department of Energy (DE-FE0007634), to efficiently and cost effectively separate carbon dioxide from the emissions of existing coal fired power plants. The CEPACS system is based on FCE’s electrochemical membrane (ECM) technology utilizing the Company’s internal reforming carbonate fuel cell products carrying the trade name of Direct FuelCell® (DFC®). The unique chemistry of carbonate fuel cells offers an innovative approach for separation of CO2 from existing fossil-fuel power plant exhaust streams (flue gases). The ECM-based CEPACS system has the potential to become a transformational CO2-separation technology by working as two devices in one: it separates the CO2 from the exhaust of other plants such as an existing coal-fired plant and simultaneously produces clean and environmentally benign (green) electric power at high efficiency using a supplementary fuel. The overall objective of this project is to successfully demonstrate the ability of FCE’s electrochemical membrane-based CEPACS system technology to separate ≥ 90% of the CO2 from a simulated Pulverized Coal (PC) power plant flue-gas stream and to compress the captured CO2 to a state that can be easily transported for sequestration or beneficial use. Also, a key project objective is to show, through a Technical and Economic Feasibility Study and bench scale testing (11.7 m2 area ECM), that the electrochemical membrane-based CEPACS system is an economical alternative for CO2 capture in PC power plants, and that it meets DOE objectives for the incremental cost of electricity (COE) for post-combustion CO2 capture.

  19. Feasibility study of using brine for carbon dioxide capture and storage from fixed sources

    SciTech Connect

    Daniel Dziedzic; Kenneth B. Gross; Robert A. Gorski; John T. Johnson

    2006-12-15

    A laboratory-scale reactor was developed to evaluate the capture of carbon dioxide (CO{sub 2}) from a gas into a liquid as an approach to control greenhouse gases emitted from fixed sources. CO{sub 2} at 5-50% concentrations was passed through a gas-exchange membrane and transferred into liquid media - tap water or simulated brine. When using water, capture efficiencies exceeded 50% and could be enhanced by adding base (e.g., sodium hydroxide) or the combination of base and carbonic anhydrase, a catalyst that speeds the conversion of CO{sub 2} to carbonic acid. The transferred CO{sub 2} formed ions, such as bicarbonate or carbonate, depending on the amount of base present. Adding precipitating cations, like Ca{sup ++}, produced insoluble carbonate salts. Simulated brine proved nearly as efficient as water in absorbing CO{sub 2}, with less than a 6% reduction in CO{sub 2} transferred. The CO{sub 2} either dissolved into the brine or formed a mixture of gas and ions. If the chemistry was favorable, carbonate precipitate spontaneously formed. Energy expenditure of pumping brine up and down from subterranean depths was modeled. We concluded that using brine in a gas-exchange membrane system for capturing CO{sub 2} from a gas stream to liquid is technically feasible and can be accomplished at a reasonable expenditure of energy. 24 refs., 9 figs., 2 tabs., 1 app.

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

    SciTech Connect

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

    2009-06-26

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

  1. Data capture and processing. [for Space Station

    NASA Technical Reports Server (NTRS)

    Lyon, John; Smith, Gene; Carper, Richard

    1987-01-01

    A systems concept developed in response to the specific requirements imposed by the Space Station and affiliated instrumentation is described. Particular attention is given to those subsystems associated with initial data capture, handling, routing, and distribution control for return link data via the Tracking and Data Relay Satellite System. The conceived approach, designated the Customer Data and Operations System, includes a data interface facility and a data handling center whose functions are data capture, demultiplexing and routing, early preprocessing, and ancillary data handling.

  2. Coprecipitated, copper-based, alumina-stabilized materials for carbon dioxide capture by chemical looping combustion.

    PubMed

    Imtiaz, Qasim; Kierzkowska, Agnieszka Marta; Müller, Christoph Rüdiger

    2012-08-01

    Chemical looping combustion (CLC) has emerged as a carbon dioxide capture and storage (CCS) process to produce a pure stream of CO(2) at very low costs when compared with alternative CCS technologies, such as scrubbing with amines. From a thermodynamic point of view, copper oxide is arguably the most promising candidate for the oxygen carrier owing to its exothermic reduction and oxidation reactions and high oxygen-carrying capacity. However, the low melting point of pure copper of only 1085 °C has so far prohibited the synthesis of copper-rich oxygen carriers. This paper is concerned with the development of copper-based and Al(2)O(3)-stabilized oxygen carriers that contain a high mass fraction of CuO, namely, 82.4 wt %. The oxygen carriers were synthesized by using a coprecipitation technique. The synthesized oxygen carriers were characterized in detail with regards to their morphological properties, chemical composition, and surface topography. It was found that both the precipitating agent and the pH at which the precipitation was performed strongly influenced the structure and chemical composition of the oxygen carriers. In addition, XRD analysis confirmed that, for the majority of the precipitation conditions investigated, CuO reacted with Al(2)O(3) to form fully reducible CuAl(2)O(4). The redox characteristics of the synthesized materials were evaluated at 800 °C by using methane as the fuel and air for reoxidation. It was found that the oxygen-carrying capacity of the synthesized oxygen carriers was strongly influenced by both the precipitating agent and the pH at which the precipitation was performed; however, all oxygen carriers tested showed a stable cyclic oxygen-carrying capacity. The oxygen carriers synthesized at pH 5.5 using NaOH or Na(2)CO(3) as the precipitating agents were the best oxygen carriers synthesized owing to their high and stable oxygen transfer and uncoupling capacities. The excellent redox characteristics of the best oxygen carrier

  3. Applications of carbon dioxide capture and storage technologies in reducing emissions from fossil-fired power plants

    SciTech Connect

    Balat, M.; Balat, H.; Oz, C.

    2009-07-01

    The aim of this paper is to investigate the global contribution of carbon capture and storage technologies to mitigating climate change. Carbon capture and storage is a technology that comprises the separation of from carbon dioxide industrial- and energy-related sources, transport to a storage location (e.g., saline aquifers and depleted hydrocarbon fields), and long-term isolation from the atmosphere. The carbon dioxides emitted directly at the power stations are reduced by 80 to 90%. In contrast, the life cycle assessment shows substantially lower reductions of greenhouse gases in total (minus 65 to 79%).

  4. PRELIMINARY ENVIRONMENTAL, HEALTH AND SAFETY RISK ASSESSMENT ON THE INTEGRATION OF A PROCESS UTILIZING LOW-ENERGY SOLVENTS FOR CARBON DIOXIDE CAPTURE ENABLED BY A COMBINATION OF ENZYMES AND VACUUM REGENERATION WITH A SUBCRITICAL PC POWER PLANT

    SciTech Connect

    Fitzgerald, David; Vidal, Rafael; Russell, Tania; Babcock, Doosan; Freeman, Charles; Bearden, Mark; Whyatt, Greg; Liu, Kun; Frimpong, Reynolds; Lu, Kunlei; Salmon, Sonja; House, Alan; Yarborough, Erin

    2014-12-31

    The results of the preliminary environmental, health and safety (EH&S) risk assessment for an enzyme-activated potassium carbonate (K2CO3) solution post-combustion CO2 capture (PCC) plant, integrated with a subcritical pulverized coal (PC) power plant, are presented. The expected emissions during normal steady-state operation have been estimated utilizing models of the PCC plant developed in AspenTech’s AspenPlus® software, bench scale test results from the University of Kentucky, and industrial experience of emission results from a slipstream PCC plant utilizing amine based solvents. A review of all potential emission species and their sources was undertaken that identified two credible emission sources, the absorber off-gas that is vented to atmosphere via a stack and the waste removed from the PCC plant in the centrifuge used to reclaim enzyme and solvent. The conditions and compositions of the emissions were calculated and the potential EH&S effects were considered as well as legislative compliance requirements. Potential mitigation methods for emissions during normal operation have been proposed and solutions to mitigate uncontrolled releases of species have been considered. The potential emissions were found to pose no significant EH&S concerns and were compliant with the Federal legislation reviewed. The limitations in predicting full scale plant performance from bench scale tests have been noted and further work on a larger scale test unit is recommended to reduce the level of uncertainty.

  5. Conceptual Design of Optimized Fossil Energy Systems with Capture and Sequestration of Carbon Dioxide

    SciTech Connect

    Nils Johnson; Joan Ogden

    2010-12-31

    In this final report, we describe research results from Phase 2 of a technical/economic study of fossil hydrogen energy systems with carbon dioxide (CO{sub 2}) capture and storage (CCS). CO{sub 2} capture and storage, or alternatively, CO{sub 2} capture and sequestration, involves capturing CO{sub 2} from large point sources and then injecting it into deep underground reservoirs for long-term storage. By preventing CO{sub 2} emissions into the atmosphere, this technology has significant potential to reduce greenhouse gas (GHG) emissions from fossil-based facilities in the power and industrial sectors. Furthermore, the application of CCS to power plants and hydrogen production facilities can reduce CO{sub 2} emissions associated with electric vehicles (EVs) and hydrogen fuel cell vehicles (HFCVs) and, thus, can also improve GHG emissions in the transportation sector. This research specifically examines strategies for transitioning to large-scale coal-derived energy systems with CCS for both hydrogen fuel production and electricity generation. A particular emphasis is on the development of spatially-explicit modeling tools for examining how these energy systems might develop in real geographic regions. We employ an integrated modeling approach that addresses all infrastructure components involved in the transition to these energy systems. The overall objective is to better understand the system design issues and economics associated with the widespread deployment of hydrogen and CCS infrastructure in real regions. Specific objectives of this research are to: Develop improved techno-economic models for all components required for the deployment of both hydrogen and CCS infrastructure, Develop novel modeling methods that combine detailed spatial data with optimization tools to explore spatially-explicit transition strategies, Conduct regional case studies to explore how these energy systems might develop in different regions of the United States, and Examine how the

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

    SciTech Connect

    Benson, Steven; Palo, Daniel; Srinivasachar, Srivats; Laudal, Daniel

    2014-12-01

    Under contract DE-FE0007603, the University of North Dakota conducted the project Evaluation of Carbon Dioxide Capture from Existing Coal Fired Plants by Hybrid Sorption Using Solid Sorbents. As an important element of this effort, an Environmental Health and Safety (EH&S) Assessment was conducted by Barr Engineering Co. (Barr) in association with the University of North Dakota. The assessment addressed air and particulate emissions as well as solid and liquid waste streams. The magnitude of the emissions and waste streams was estimated for evaluation purposes. EH&S characteristics of materials used in the system are also described. This document contains data based on the mass balances from both the 40 kJ/mol CO2 and 80 kJ/mol CO2 desorption energy cases evaluated in the Final Technical and Economic Feasibility study also conducted by Barr Engineering.

  7. Super liquid-repellent gas membranes for carbon dioxide capture and heart-lung machines.

    PubMed

    Paven, Maxime; Papadopoulos, Periklis; Schöttler, Susanne; Deng, Xu; Mailänder, Volker; Vollmer, Doris; Butt, Hans-Jürgen

    2013-01-01

    In a gas membrane, gas is transferred between a liquid and a gas through a microporous membrane. The main challenge is to achieve a high gas transfer while preventing wetting and clogging. With respect to the oxygenation of blood, haemocompatibility is also required. Here we coat macroporous meshes with a superamphiphobic-or liquid repellent-layer to meet this challenge. The superamphiphobic layer consists of a fractal-like network of fluorinated silicon oxide nanospheres; gas trapped between the nanospheres keeps the liquid from contacting the wall of the membrane. We demonstrate the capabilities of the membrane by capturing carbon dioxide gas into a basic aqueous solution and in addition use it to oxygenate blood. Usually, blood tends to clog membranes because of the abundance of blood cells, platelets, proteins and lipids. We show that human blood stored in a superamphiphobic well for 24 h can be poured off without leaving cells or adsorbed protein behind.

  8. Super liquid-repellent gas membranes for carbon dioxide capture and heart–lung machines

    PubMed Central

    Paven, Maxime; Papadopoulos, Periklis; Schöttler, Susanne; Deng, Xu; Mailänder, Volker; Vollmer, Doris; Butt, Hans-Jürgen

    2013-01-01

    In a gas membrane, gas is transferred between a liquid and a gas through a microporous membrane. The main challenge is to achieve a high gas transfer while preventing wetting and clogging. With respect to the oxygenation of blood, haemocompatibility is also required. Here we coat macroporous meshes with a superamphiphobic—or liquid repellent—layer to meet this challenge. The superamphiphobic layer consists of a fractal-like network of fluorinated silicon oxide nanospheres; gas trapped between the nanospheres keeps the liquid from contacting the wall of the membrane. We demonstrate the capabilities of the membrane by capturing carbon dioxide gas into a basic aqueous solution and in addition use it to oxygenate blood. Usually, blood tends to clog membranes because of the abundance of blood cells, platelets, proteins and lipids. We show that human blood stored in a superamphiphobic well for 24 h can be poured off without leaving cells or adsorbed protein behind. PMID:24065073

  9. Selective and Regenerative Carbon Dioxide Capture by Highly Polarizing Porous Carbon Nitride.

    PubMed

    Oh, Youngtak; Le, Viet-Duc; Maiti, Uday Narayan; Hwang, Jin Ok; Park, Woo Jin; Lim, Joonwon; Lee, Kyung Eun; Bae, Youn-Sang; Kim, Yong-Hyun; Kim, Sang Ouk

    2015-09-22

    Energy-efficient CO2 capture is a stringent demand for green and sustainable energy supply. Strong adsorption is desirable for high capacity and selective capture at ambient conditions but unfavorable for regeneration of adsorbents by a simple pressure control process. Here we present highly regenerative and selective CO2 capture by carbon nitride functionalized porous reduced graphene oxide aerogel surface. The resultant structure demonstrates large CO2 adsorption capacity at ambient conditions (0.43 mmol·g(-1)) and high CO2 selectivity against N2 yet retains regenerability to desorb 98% CO2 by simple pressure swing. First-principles thermodynamics calculations revealed that microporous edges of graphitic carbon nitride offer the optimal CO2 adsorption by induced dipole interaction and allows excellent CO2 selectivity as well as facile regenerability. This work identifies a customized route to reversible gas capture using metal-free, two-dimensional carbonaceous materials, which can be extended to other useful applications.

  10. Ambient carbon dioxide capture by boron-rich boron nitride nanotube.

    PubMed

    Choi, Heechol; Park, Young Choon; Kim, Yong-Hyun; Lee, Yoon Sup

    2011-02-23

    Carbon dioxides (CO(2)) emitted from large-scale coal-fired power stations or industrial manufacturing plants have to be properly captured to minimize environmental side effects. From results of ab initio calculations using plane waves [PAW-PBE] and localized atomic orbitals [ONIOM(wB97X-D/6-31G*:AM1)], we report strong CO(2) adsorption on boron antisite (B(N)) in boron-rich boron nitride nanotube (BNNT). We have identified two adsorption states: (1) A linear CO(2) molecule is physically adsorbed on the B(N), showing electron donation from the CO(2) lone-pair states to the B(N) double-acceptor state, and (2) the physisorbed CO(2) undergoes a carboxylate-like structural distortion and C═O π-bond breaking due to electron back-donation from B(N) to CO(2). The CO(2) chemisorption energy on B(N) is almost independent of tube diameter and, more importantly, higher than the standard free energy of gaseous CO(2) at room temperature. This implies that boron-rich BNNT could capture CO(2) effectively at ambient conditions. PMID:21287992

  11. Novel Application of Carbonate Fuel Cell for Capturing Carbon Dioxide from Flue Gas Streams

    SciTech Connect

    Jolly, Stephen; Ghezel-Ayagh, Hossein; Willman, Carl; Patel, Dilip; DiNitto, M.; Marina, Olga A.; Pederson, Larry R.; Steen, William A.

    2015-09-30

    To address concerns about climate change resulting from emission of CO2 by coal-fueled power plants, FuelCell Energy, Inc. has developed the Combined Electric Power and Carbon-dioxide Separation (CEPACS) system concept. The CEPACS system utilizes Electrochemical Membrane (ECM) technology derived from the Company’s Direct FuelCell® products. The system separates the CO2 from the flue gas of other plants and produces electric power using a supplementary fuel. FCE is currently evaluating the use of ECM to cost effectively separate CO2 from the flue gas of Pulverized Coal (PC) power plants under a U.S. Department of Energy contract. The overarching objective of the project is to verify that the ECM can achieve at least 90% CO2 capture from the flue gas with no more than 35% increase in the cost of electricity. The project activities include: 1) laboratory scale operational and performance tests of a membrane assembly, 2) performance tests of the membrane to evaluate the effects of impurities present in the coal plant flue gas, in collaboration with Pacific Northwest National Laboratory, 3) techno-economic analysis for an ECM-based CO2 capture system applied to a 550 MW existing PC plant, in partnership with URS Corporation, and 4) bench scale (11.7 m2 area) testing of an ECM-based CO2 separation and purification system.

  12. High Temperature Polybenzimidazole Hollow Fiber Membranes for Hydrogen Separation and Carbon Dioxide Capture from Synthesis Gas

    SciTech Connect

    Singh, Rajinder P.; Dahe, Ganpat J.; Dudeck, Kevin W.; Welch, Cynthia F.; Berchtold, Kathryn A.

    2014-12-31

    Sustainable reliance on hydrocarbon feedstocks for energy generation requires CO₂ separation technology development for energy efficient carbon capture from industrial mixed gas streams. High temperature H₂ selective glassy polymer membranes are an attractive option for energy efficient H₂/CO₂ separations in advanced power production schemes with integrated carbon capture. They enable high overall process efficiencies by providing energy efficient CO₂ separations at process relevant operating conditions and correspondingly, minimized parasitic energy losses. Polybenzimidazole (PBI)-based materials have demonstrated commercially attractive H₂/CO₂ separation characteristics and exceptional tolerance to hydrocarbon fuel derived synthesis (syngas) gas operating conditions and chemical environments. To realize a commercially attractive carbon capture technology based on these PBI materials, development of high performance, robust PBI hollow fiber membranes (HFMs) is required. In this work, we discuss outcomes of our recent efforts to demonstrate and optimize the fabrication and performance of PBI HFMs for use in pre-combustion carbon capture schemes. These efforts have resulted in PBI HFMs with commercially attractive fabrication protocols, defect minimized structures, and commercially attractive permselectivity characteristics at IGCC syngas process relevant conditions. The H₂/CO₂ separation performance of these PBI HFMs presented in this document regarding realistic process conditions is greater than that of any other polymeric system reported to-date.

  13. High Temperature Polybenzimidazole Hollow Fiber Membranes for Hydrogen Separation and Carbon Dioxide Capture from Synthesis Gas

    DOE PAGESBeta

    Singh, Rajinder P.; Dahe, Ganpat J.; Dudeck, Kevin W.; Welch, Cynthia F.; Berchtold, Kathryn A.

    2014-12-31

    Sustainable reliance on hydrocarbon feedstocks for energy generation requires CO₂ separation technology development for energy efficient carbon capture from industrial mixed gas streams. High temperature H₂ selective glassy polymer membranes are an attractive option for energy efficient H₂/CO₂ separations in advanced power production schemes with integrated carbon capture. They enable high overall process efficiencies by providing energy efficient CO₂ separations at process relevant operating conditions and correspondingly, minimized parasitic energy losses. Polybenzimidazole (PBI)-based materials have demonstrated commercially attractive H₂/CO₂ separation characteristics and exceptional tolerance to hydrocarbon fuel derived synthesis (syngas) gas operating conditions and chemical environments. To realize a commerciallymore » attractive carbon capture technology based on these PBI materials, development of high performance, robust PBI hollow fiber membranes (HFMs) is required. In this work, we discuss outcomes of our recent efforts to demonstrate and optimize the fabrication and performance of PBI HFMs for use in pre-combustion carbon capture schemes. These efforts have resulted in PBI HFMs with commercially attractive fabrication protocols, defect minimized structures, and commercially attractive permselectivity characteristics at IGCC syngas process relevant conditions. The H₂/CO₂ separation performance of these PBI HFMs presented in this document regarding realistic process conditions is greater than that of any other polymeric system reported to-date.« less

  14. Acid sorption regeneration process using carbon dioxide

    DOEpatents

    King, C. Judson; Husson, Scott M.

    2001-01-01

    Carboxylic acids are sorbed from aqueous feedstocks onto a solid adsorbent in the presence of carbon dioxide under pressure. The acids are freed from the sorbent phase by a suitable regeneration method, one of which is treating them with an organic alkylamine solution thus forming an alkylamine-carboxylic acid complex which thermally decomposes to the desired carboxylic acid and the alkylamine.

  15. Functionalization of Metal-Organic Frameworks for Enhanced Stability under Humid Carbon Dioxide Capture Conditions.

    PubMed

    Andirova, Dinara; Lei, Yu; Zhao, Xiaodan; Choi, Sunho

    2015-10-26

    Metal-organic frameworks (MOFs) have been highlighted recently as promising materials for CO2 capture. However, in practical CO2 capture processes, such as capture from flue gas or ambient air, the adsorption properties of MOFs tend to be harmed by the presence of moisture possibly because of the hydrophilic nature of the coordinatively unsaturated sites (CUSs) within their framework. In this work, the CUSs of the MOF framework are functionalized with amine-containing molecules to prevent structural degradation in a humid environment. Specifically, the framework of the magnesium dioxybenzenedicarboxylate (Mg/DOBDC) MOF was functionalized with ethylenediamine (ED) molecules to make the overall structure less hydrophilic. Structural analysis after exposure to high-temperature steam showed that the ED-functionalized Mg/DOBDC (ED-Mg/DOBDC) is more stable under humid conditions, than Mg/DOBDC, which underwent drastic structural changes. ED-Mg/DOBDC recovered its CO2 adsorption capacity and initial adsorption rate quite well as opposed to the original Mg/DOBDC, which revealed a significant reduction in its capture capacity and kinetics. These results suggest that the amine-functionalization of the CUSs is an effective way to enhance the structural stability of MOFs as well as their capture of humid CO2 . PMID:26367016

  16. Functionalization of Metal-Organic Frameworks for Enhanced Stability under Humid Carbon Dioxide Capture Conditions.

    PubMed

    Andirova, Dinara; Lei, Yu; Zhao, Xiaodan; Choi, Sunho

    2015-10-26

    Metal-organic frameworks (MOFs) have been highlighted recently as promising materials for CO2 capture. However, in practical CO2 capture processes, such as capture from flue gas or ambient air, the adsorption properties of MOFs tend to be harmed by the presence of moisture possibly because of the hydrophilic nature of the coordinatively unsaturated sites (CUSs) within their framework. In this work, the CUSs of the MOF framework are functionalized with amine-containing molecules to prevent structural degradation in a humid environment. Specifically, the framework of the magnesium dioxybenzenedicarboxylate (Mg/DOBDC) MOF was functionalized with ethylenediamine (ED) molecules to make the overall structure less hydrophilic. Structural analysis after exposure to high-temperature steam showed that the ED-functionalized Mg/DOBDC (ED-Mg/DOBDC) is more stable under humid conditions, than Mg/DOBDC, which underwent drastic structural changes. ED-Mg/DOBDC recovered its CO2 adsorption capacity and initial adsorption rate quite well as opposed to the original Mg/DOBDC, which revealed a significant reduction in its capture capacity and kinetics. These results suggest that the amine-functionalization of the CUSs is an effective way to enhance the structural stability of MOFs as well as their capture of humid CO2 .

  17. Post combustion carbon dioxide capture using amine functionalized carbon nanotubes: A review

    NASA Astrophysics Data System (ADS)

    Dash, Sukanta K.

    2016-04-01

    Many technological viable options available for post combustion CO2 capture (PCC) from fossil fuel based power plants, such as amine absorption, adsorption, membrane separation, cryogenic separation processes. Out of these technological pathways adsorption using carbon nanotubes (CNTs) has shown potential advantages compared to other techniques for CO2 capture from flue gas streams which is evident form published literature from various research groups. Considering the recent developments, this work presents a state-of-the-art review on CO2 capture process using CNTs, amine functionalized CNTs and membrane based CNTs. One of the major challenges in developing CNT adsorption technology lies in the choice and development of an adsorbent material that can efficiently adsorb and also easily desorb and concentrate the captured CO2 with low energy input. This review work consists of a number of interdisciplinary research activities that are focused on the feasibility of developing a small scale carbon capture and storage (CCS) based on the adsorption properties of chemically functionalized CNTs. Another recent development for CO2 separation from flue gas is the application of membrane-based CNTs. Membrane based CO2 separation invites several advantages such as no need of an additional chemical or physical solvent; low energy use; simple process, hence easy to operate. In this work analysis and literature reviews carried out in the recent development in CNTs and membrane based CNTs for CO2 adsorption and separation to update the recent progress in this area. Finally a comparison with amine absorption process and retrofitting option has been discussed with few recommendations.

  18. New Demands, New Supplies: A National Look at the Water Balance of Carbon Dioxide Capture and Sequestration

    NASA Astrophysics Data System (ADS)

    Roach, J. D.; Kobos, P.; Klise, G. T.; Krumhansl, J. L.; McNemar, A.

    2010-12-01

    Concerns over rising concentrations of greenhouse gases in the atmosphere have resulted in serious consideration of policies aimed at reduction of anthropogenic carbon dioxide (CO2) emissions. If large scale abatement efforts are undertaken, one critical tool will be geologic sequestration of CO2 captured from large point sources, specifically coal and natural gas fired power plants. Current CO2 capture technologies exact a substantial energy penalty on the source power plant, which must be offset with make-up power. Water demands increase at the source plant due to added cooling loads. In addition, new water demand is created by water requirements associated with generation of the make-up power. At the sequestration site however, saline water may be extracted to manage CO2 plum migration and pressure build up in the geologic formation. Thus, while CO2 capture creates new water demands, CO2 sequestration has the potential to create new supplies. Some or all of the added demand may be offset by treatment and use of the saline waters extracted from geologic formations during CO2 sequestration. Sandia National Laboratories, with guidance and support from the National Energy Technology Laboratory, is creating a model to evaluate the potential for a combined approach to saline formations, as a sink for CO2 and a source for saline waters that can be treated and beneficially reused to serve power plant water demands. This presentation will focus on the magnitude of added U.S. power plant water demand under different CO2 emissions reduction scenarios, and the portion of added demand that might be offset by saline waters extracted during the CO2 sequestration process. 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.

  19. New demands, new supplies : a national look at the water balance of carbon dioxide capture and sequestration.

    SciTech Connect

    Krumhansl, James Lee; McNemar, Andrea , Morgantown, WV); Kobos, Peter Holmes; Roach, Jesse Dillon; Klise, Geoffrey Taylor

    2010-12-01

    Concerns over rising concentrations of greenhouse gases in the atmosphere have resulted in serious consideration of policies aimed at reduction of anthropogenic carbon dioxide (CO2) emissions. If large scale abatement efforts are undertaken, one critical tool will be geologic sequestration of CO2 captured from large point sources, specifically coal and natural gas fired power plants. Current CO2 capture technologies exact a substantial energy penalty on the source power plant, which must be offset with make-up power. Water demands increase at the source plant due to added cooling loads. In addition, new water demand is created by water requirements associated with generation of the make-up power. At the sequestration site however, saline water may be extracted to manage CO2 plum migration and pressure build up in the geologic formation. Thus, while CO2 capture creates new water demands, CO2 sequestration has the potential to create new supplies. Some or all of the added demand may be offset by treatment and use of the saline waters extracted from geologic formations during CO2 sequestration. Sandia National Laboratories, with guidance and support from the National Energy Technology Laboratory, is creating a model to evaluate the potential for a combined approach to saline formations, as a sink for CO2 and a source for saline waters that can be treated and beneficially reused to serve power plant water demands. This presentation will focus on the magnitude of added U.S. power plant water demand under different CO2 emissions reduction scenarios, and the portion of added demand that might be offset by saline waters extracted during the CO2 sequestration process.

  20. Early atmospheric detection of carbon dioxide from carbon capture and storage sites

    PubMed Central

    Pak, Nasrin Mostafavi; Rempillo, Ofelia; Norman, Ann-Lise; Layzell, David B.

    2016-01-01

    ABSTRACT The early atmospheric detection of carbon dioxide (CO2) leaks from carbon capture and storage (CCS) sites is important both to inform remediation efforts and to build and maintain public support for CCS in mitigating greenhouse gas emissions. A gas analysis system was developed to assess the origin of plumes of air enriched in CO2, as to whether CO2 is from a CCS site or from the oxidation of carbon compounds. The system measured CO2 and O2 concentrations for different plume samples relative to background air and calculated the gas differential concentration ratio (GDCR = −ΔO2/ΔCO2). The experimental results were in good agreement with theoretical calculations that placed GDCR values for a CO2 leak at 0.21, compared with GDCR values of 1–1.8 for the combustion of carbon compounds. Although some combustion plume samples deviated in GDCR from theoretical, the very low GDCR values associated with plumes from CO2 leaks provided confidence that this technology holds promise in providing a tool for the early detection of CO2 leaks from CCS sites.  Implications: This work contributes to the development of a cost-effective technology for the early detection of leaks from sites where CO2 has been injected into the subsurface to enhance oil recovery or to permanently store the gas as a strategy for mitigating climate change. Such technology will be important in building public confidence regarding the safety and security of carbon capture and storage sites. PMID:27111469

  1. Surface modification of oil fly ash and its application in selective capturing of carbon dioxide

    NASA Astrophysics Data System (ADS)

    Yaumi, Ali L.; Hussien, Ibnelwaleed A.; Shawabkeh, Reyad A.

    2013-02-01

    Oil fly ash from power generation plants was activated with 30% NH4OH and used for selective adsorption of carbon dioxide from CO2/N2 mixture. The treated samples were characterized for their surface area, morphology, crystalline phase, chemical composition and surface functional groups. Energy dispersive X-ray analysis showed an increase in the carbon contents from 45 to 73 wt% as a result of leaching out metal oxides. XRD proved that chemical activation of ash resulted in diminishing of major crystalline phases of zeolite, and other alumino-silicates leaving only quartz and mullite. BET analysis showed an increase in surface area from 59 to 318 m2/g after chemical activation and the pore volume increased from 0.0368 to 0.679 cm3/g. This increase in pore volume is supported by the results of SEM, where more micropores were opened with well-defined particle sizes and porous structure. The TGA of the treated fly ash showed stability at higher temperature as the weight loss decreased with increasing temperature. For treated ash, the FTIR displayed new peaks of amine functional group. The treated ash was used for the removal of CO2 from CO2/N2 mixture and the maximum adsorption/capturing capacity was found to be 240 mg/g. This capacity increases with increase in initial gas concentration, inlet flow rate and temperature suggesting the endothermic nature of the interaction between the gas molecules and the surface of the ash.

  2. Temporal and Spatial Deployment of Carbon Dioxide Capture and Storage Technologies across the Representative Concentration Pathways

    SciTech Connect

    Dooley, James J.; Calvin, Katherine V.

    2011-04-18

    The Intergovernmental Panel on Climate Change’s (IPCC) Fifth Assessment (to be published in 2013-2014) will to a significant degree be built around four Representative Concentration Pathways (RCPs) that are intended to represent four scenarios of future development of greenhouse gas emissions, land use, and concentrations that span the widest range of potential future atmospheric radiative forcing. Under the very stringent climate policy implied by the 2.6 W/m2 overshoot scenario, all electricity is eventually generated from low carbon sources. However, carbon dioxide capture and storage (CCS) technologies never comprise more than 50% of total electricity generation in that very stringent scenario or in any of the other cases examined here. There are significant differences among the cases studied here in terms of how CCS technologies are used, with the most prominent being is the significant expansion of biomass+CCS as the stringency of the implied climate policy increases. Cumulative CO2 storage across the three cases that imply binding greenhouse gas constraints ranges by nearly an order of magnitude from 170GtCO2 (radiative forcing of 6.0W/m2 in 2100) to 1600GtCO2 (2.6W/m2 in 2100) over the course of this century. This potential demand for deep geologic CO2 storage is well within published estimates of total global CO2 storage capacity.

  3. Sensitivity studies for the weak r process: neutron capture rates

    SciTech Connect

    Surman, R.; Mumpower, M.; Sinclair, R.; Jones, K. L.; Hix, W. R.; McLaughlin, G. C.

    2014-04-15

    Rapid neutron capture nucleosynthesis involves thousands of nuclear species far from stability, whose nuclear properties need to be understood in order to accurately predict nucleosynthetic outcomes. Recently sensitivity studies have provided a deeper understanding of how the r process proceeds and have identified pieces of nuclear data of interest for further experimental or theoretical study. A key result of these studies has been to point out the importance of individual neutron capture rates in setting the final r-process abundance pattern for a ‘main’ (A ∼ 130 peak and above) r process. Here we examine neutron capture in the context of a ‘weak’ r process that forms primarily the A ∼ 80 r-process abundance peak. We identify the astrophysical conditions required to produce this peak region through weak r-processing and point out the neutron capture rates that most strongly influence the final abundance pattern.

  4. Selective and Regenerative Carbon Dioxide Capture by Highly Polarizing Porous Carbon Nitride.

    PubMed

    Oh, Youngtak; Le, Viet-Duc; Maiti, Uday Narayan; Hwang, Jin Ok; Park, Woo Jin; Lim, Joonwon; Lee, Kyung Eun; Bae, Youn-Sang; Kim, Yong-Hyun; Kim, Sang Ouk

    2015-09-22

    Energy-efficient CO2 capture is a stringent demand for green and sustainable energy supply. Strong adsorption is desirable for high capacity and selective capture at ambient conditions but unfavorable for regeneration of adsorbents by a simple pressure control process. Here we present highly regenerative and selective CO2 capture by carbon nitride functionalized porous reduced graphene oxide aerogel surface. The resultant structure demonstrates large CO2 adsorption capacity at ambient conditions (0.43 mmol·g(-1)) and high CO2 selectivity against N2 yet retains regenerability to desorb 98% CO2 by simple pressure swing. First-principles thermodynamics calculations revealed that microporous edges of graphitic carbon nitride offer the optimal CO2 adsorption by induced dipole interaction and allows excellent CO2 selectivity as well as facile regenerability. This work identifies a customized route to reversible gas capture using metal-free, two-dimensional carbonaceous materials, which can be extended to other useful applications. PMID:26267150

  5. Computational evaluation of metal-organic frameworks for carbon dioxide capture

    NASA Astrophysics Data System (ADS)

    Yu, Jiamei

    Metal-organic frameworks (MOFs), a new class of porous solids comprised of metal-containing nodes linked by organic ligands, have become promising materials for gas separations. In particular, their flexible chemistry makes them attractive for CO2 capture from flue gas streams in post-combustion plants. Although numerous efforts have been exerted on the investigation of MOFs for CO2 capture, the exploration of the effects from coexisting components present in very dilute proportions in flue gases is limited because of the experimental difficulty to determine the coadsorption of CO2 with trace components. In this regard, molecular simulations show superiority. In this study, molecular simulations are used to estimate the influence of impurities: water, O2, and SO2 on post-combustion CO2 capture in MOFs. Firstly, two MOFs with coordinatively unsaturated metal sites (CUMs), HKUST-1 and Mg-MOF-74 are explored. Increase of CO 2 adsorption is observed for hydrated HKUST-1; on the contrary, the opposite water adsorption behavior is observed in hydrated Mg-MOF-74, leading to decrease of CO2 adsorption. Further, water effects on CO 2 capture in M-HKUST1 (M = Mg, Zn, Co, Ni) are evaluated to test whether comparing the binding energy could be a general method to evaluate water effects in MOFs with CUMs. It is found that the method works well for Zn-, Co-, and Ni-HKUST1 but partially for Mg-HKUST1. In addition, the effects of O2 and SO2 on CO2 capture in MOFs are also investigated for the first time, showing that the effects of O2 may be negligible but SO2 has negative effects in the CO 2 capture process in HKUST-1 systems. Secondly, the influences of water on CO2 capture in three UiO-66 MOFs with functional groups, --NH2, --OH and --Br are explored, respectively. For UiO-66-NH2 and -OH, the presence of water lowers CO2 adsorption significantly; in contrast, water shows much smaller effects in UiO-66-Br. Moreover, the presence of SO 2 decreases water adsorption but enhances CO

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

    SciTech Connect

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

    2009-12-01

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

  7. Evaluation of Carbon Dioxide Capture From Existing Coal Fired Plants by Hybrid Sorption Using Solid Sorbents

    SciTech Connect

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

    2014-12-31

    A novel hybrid solid sorbent technology for CO₂ capture and separation from coal combustion-derived flue gas was evaluated. The technology – Capture of CO₂ by Hybrid Sorption (CACHYS™) – is a solid sorbent technology based on the following ideas: 1) reduction of energy for sorbent regeneration, 2) utilization of novel process chemistry, 3) contactor conditions that minimize sorbent-CO₂ heat of reaction and promote fast CO₂ capture, and 4) low-cost method of heat management. This report provides key information developed during the course of the project that includes sorbent performance, energy for sorbent regeneration, physical properties of the sorbent, the integration of process components, sizing of equipment, and overall capital and operational cost of the integrated CACHYS™ system. Seven sorbent formulations were prepared and evaluated at the lab-scale for energy requirements and CO₂ capture performance. Sorbent heat of regeneration ranged from 30-80 kJ/mol CO₂ and was found to be dependent on process conditions. Two sorbent formulations (designated HCK-4 & HCK-7) were down-selected for additional fixed-bed testing. Additional testing involved subjecting the sorbents to 100 continuous cycles in the fixed-bed reactor to determine performance as a function of time. The working capacity achieved for HCK-4 sorbent ranged from 5.5-8.0 g CO₂/100 g sorbent, while the HCK-7 typically ranged from 8.0-10.0 g CO₂/100 g sorbent. Overall, there was no deterioration in capacity with continuous cycling for either sorbent. The CACHYS™ bench-scale testing system designed and fabricated under this award consists of a dual circulating fluidized-bed adsorber and a moving-bed regenerator. The system takes a flue gas slipstream from the University of North Dakota’s coal-fired steam plant. Prior to being sent to the adsorber, the flue gas is scrubbed to remove SO₂ and particulate. During parametric testing of the adsorber, CO₂ capture achieved using

  8. Adsorbent materials for carbon dioxide capture from large anthropogenic point sources.

    PubMed

    Choi, Sunho; Drese, Jeffrey H; Jones, Christopher W

    2009-01-01

    Since the time of the industrial revolution, the atmospheric CO(2) concentration has risen by nearly 35 % to its current level of 383 ppm. The increased carbon dioxide concentration in the atmosphere has been suggested to be a leading contributor to global climate change. To slow the increase, reductions in anthropogenic CO(2) emissions are necessary. Large emission point sources, such as fossil-fuel-based power generation facilities, are the first targets for these reductions. A benchmark, mature technology for the separation of dilute CO(2) from gas streams is via absorption with aqueous amines. However, the use of solid adsorbents is now being widely considered as an alternative, potentially less-energy-intensive separation technology. This Review describes the CO(2) adsorption behavior of several different classes of solid carbon dioxide adsorbents, including zeolites, activated carbons, calcium oxides, hydrotalcites, organic-inorganic hybrids, and metal-organic frameworks. These adsorbents are evaluated in terms of their equilibrium CO(2) capacities as well as other important parameters such as adsorption-desorption kinetics, operating windows, stability, and regenerability. The scope of currently available CO(2) adsorbents and their critical properties that will ultimately affect their incorporation into large-scale separation processes is presented.

  9. Shallow Processing and Attention Capture in Written and Spoken Discourse

    ERIC Educational Resources Information Center

    Sanford, Alison J. S.; Sanford, Anthony J.; Molle, Jo; Emmott, Catherine

    2006-01-01

    Processing of discourse seems to be far from uniform with much evidence indicating that it can be quite shallow. The question is then what modulates depth of processing? A range of discourse devices exist that we believe may lead to more detailed processing of language input (Attention Capturers), thus serving as modulators of processing enabling…

  10. METAL CAPTURE BY SORBENTS IN COMBUSTION PROCESSES

    EPA Science Inventory

    The article gives results of an investigation of the use of sorbents to control trace metal emissions from combustion processes and an exploration of the underlying mechanisms. mphasis was on mechanisms in which the metal vapor was reactively scavenged by simple commercial sorben...

  11. Composite Membranes for CO2 Capture: High Performance Metal Organic Frameworks/Polymer Composite Membranes for Carbon Dioxide Capture

    SciTech Connect

    2010-07-01

    IMPACCT Project: A team of six faculty members at Georgia Tech are developing an enhanced membrane by fitting metal organic frameworks, compounds that show great promise for improved carbon capture, into hollow fiber membranes. This new material would be highly efficient at removing CO2 from the flue gas produced at coal-fired power plants. The team is analyzing thousands of metal organic frameworks to identify those that are most suitable for carbon capture based both on their ability to allow coal exhaust to pass easily through them and their ability to select CO2 from that exhaust for capture and storage. The most suitable frameworks would be inserted into the walls of the hollow fiber membranes, making the technology readily scalable due to their high surface area. This composite membrane would be highly stable, withstanding the harsh gas environment found in coal exhaust.

  12. Transport Properties of Amine/Carbon Dioxide Reactive Mixtures and Implications to Carbon Capture Technologies.

    PubMed

    Turgman-Cohen, Salomon; Giannelis, Emmanuel P; Escobedo, Fernando A

    2015-08-19

    The structure and transport properties of physisorbed and chemisorbed CO2 in model polyamine liquids (hexamethylenediamine and diethylenetriamine) are studied via molecular dynamics simulations. Such systems are relevant to CO2 absorption processes where nonaqueous amines are used as absorbents (e.g., when impregnated or grafted onto mesoporous media or misted in the gas phase). It is shown that accounting for the ionic speciation resulting from CO2 chemisorption enabled us to capture the qualitative changes in extent of absorption and fluidity with time that are observed in thermogravimetric experiments. Simulations reveal that high enough concentration of reacted CO2 leads to strong intermolecular ionic interactions and the arrest of molecular translations. The transport properties obtained from the simulations of the ionic speciated mixtures are also used to construct an approximate continuum-level model for the CO2 absorption process that mimics thermogravimetric experiments.

  13. Transport Properties of Amine/Carbon Dioxide Reactive Mixtures and Implications to Carbon Capture Technologies.

    PubMed

    Turgman-Cohen, Salomon; Giannelis, Emmanuel P; Escobedo, Fernando A

    2015-08-19

    The structure and transport properties of physisorbed and chemisorbed CO2 in model polyamine liquids (hexamethylenediamine and diethylenetriamine) are studied via molecular dynamics simulations. Such systems are relevant to CO2 absorption processes where nonaqueous amines are used as absorbents (e.g., when impregnated or grafted onto mesoporous media or misted in the gas phase). It is shown that accounting for the ionic speciation resulting from CO2 chemisorption enabled us to capture the qualitative changes in extent of absorption and fluidity with time that are observed in thermogravimetric experiments. Simulations reveal that high enough concentration of reacted CO2 leads to strong intermolecular ionic interactions and the arrest of molecular translations. The transport properties obtained from the simulations of the ionic speciated mixtures are also used to construct an approximate continuum-level model for the CO2 absorption process that mimics thermogravimetric experiments. PMID:26200117

  14. A Process for Capturing the Art of Systems Engineering

    NASA Technical Reports Server (NTRS)

    Owens, Clark V., III; Sekeres, Carrie; Roumie, Yasmeen

    2016-01-01

    There is both an art and a science to systems engineering. The science of systems engineering is effectively captured in processes and procedures, but the art is much more elusive. We propose that there is six step process that can be applied to any systems engineering organization to create an environment from which the "art" of that organization can be captured, be allowed to evolve collaboratively and be shared with all members of the organization. This paper details this process as it was applied to NASA Launch Services Program (LSP) Integration Engineering Branch during a pilot program of Confluence, a Commercial Off The Shelf (COTS) wiki tool.

  15. Neutron Capture Rates and r-PROCESS Nucleosynthesis

    NASA Astrophysics Data System (ADS)

    Surman, R. A.; Mumpower, M. R.; McLaughlin, G. C.; Sinclair, R.; Hix, W. R.; Jones, K. L.

    2013-03-01

    Simulations of r-process nucleosynthesis require nuclear physics information for thousands of neutron-rich nuclear species from the line of stability to the neutron drip line. While arguably the most important pieces of nuclear data for the r-process are the masses and β decay rates, individual neutron capture rates can also be of key importance in setting the final r-process abundance pattern. Here we consider the influence of neutron capture rates in forming the A ~ 80 and rare earth peaks.

  16. Process for separating carbon dioxide from flue gas using sweep-based membrane separation and absorption steps

    DOEpatents

    Wijmans, Johannes G.; Baker, Richard W.; Merkel, Timothy C.

    2012-08-21

    A gas separation process for treating flue gases from combustion processes, and combustion processes including such gas separation. The invention involves routing a first portion of the flue gas stream to be treated to an absorption-based carbon dioxide capture step, while simultaneously flowing a second portion of the flue gas across the feed side of a membrane, flowing a sweep gas stream, usually air, across the permeate side, then passing the permeate/sweep gas to the combustor.

  17. Capture process in nuclear reactions with a quantum master equation

    SciTech Connect

    Sargsyan, V. V.; Kanokov, Z.; Adamian, G. G.; Antonenko, N. V.; Scheid, W.

    2009-09-15

    Projectile-nucleus capture by a target nucleus at bombarding energies in the vicinity of the Coulomb barrier is treated with the reduced-density-matrix formalism. The effects of dissipation and fluctuations on the capture process are taken self-consistently into account within the quantum model suggested. The excitation functions for the capture in the reactions {sup 16}O, {sup 19}F, {sup 26}Mg, {sup 28}Si, {sup 32,34,36,38}S, {sup 40,48}Ca, {sup 50}Ti, {sup 52}Cr+{sup 208}Pb with spherical nuclei are calculated and compared with the experimental data. At bombarding energies about (15-25) MeV above the Coulomb barrier the maximum of capture cross section is revealed for the {sup 58}Ni+{sup 208}Pb reaction.

  18. Exposures to carbon dioxide in the poultry processing industry

    SciTech Connect

    Jacobs, D.E.; Smith, M.S.

    1988-12-01

    The use of dry ice has increased dramatically in poultry processing plants because of changes in the fast food industry. Concentrations of carbon dioxide in four such plants were measured and were found to exceed the Immediately Dangerous to Life and Health Level (50,000 ppm) inside holding coolers where ventilation is poor. In other areas, where dry ice is delivered to poultry packages, time-weighted average exposures can exceed the threshold limit value of 5000 ppm by substantial margins, even if local exhaust ventilation systems are present. Reports of adverse health effects from carbon dioxide exposure and various control measures are reviewed. Recommendations regarding sampling and analytical techniques also are presented. Operators of poultry plants where dry ice is used need to recognize the occupational hazards of exposure to carbon dioxide.

  19. Easily regenerable solid adsorbents based on polyamines for carbon dioxide capture from the air.

    PubMed

    Goeppert, Alain; Zhang, Hang; Czaun, Miklos; May, Robert B; Prakash, G K Surya; Olah, George A; Narayanan, S R

    2014-05-01

    Adsorbents prepared easily by impregnation of fumed silica with polyethylenimine (PEI) are promising candidates for the capture of CO2 directly from the air. These inexpensive adsorbents have high CO2 adsorption capacity at ambient temperature and can be regenerated in repeated cycles under mild conditions. Despite the very low CO2 concentration, they are able to scrub efficiently all CO2 out of the air in the initial hours of the experiments. The influence of parameters such as PEI loading, adsorption and desorption temperature, particle size, and PEI molecular weight on the adsorption behavior were investigated. The mild regeneration temperatures required could allow the use of waste heat available in many industrial processes as well as solar heat. CO2 adsorption from the air has a number of applications. Removal of CO2 from a closed environment, such as a submarine or space vehicles, is essential for life support. The supply of CO2-free air is also critical for alkaline fuel cells and batteries. Direct air capture of CO2 could also help mitigate the rising concerns about atmospheric CO2 concentration and associated climatic changes, while, at the same time, provide the first step for an anthropogenic carbon cycle.

  20. Easily regenerable solid adsorbents based on polyamines for carbon dioxide capture from the air.

    PubMed

    Goeppert, Alain; Zhang, Hang; Czaun, Miklos; May, Robert B; Prakash, G K Surya; Olah, George A; Narayanan, S R

    2014-05-01

    Adsorbents prepared easily by impregnation of fumed silica with polyethylenimine (PEI) are promising candidates for the capture of CO2 directly from the air. These inexpensive adsorbents have high CO2 adsorption capacity at ambient temperature and can be regenerated in repeated cycles under mild conditions. Despite the very low CO2 concentration, they are able to scrub efficiently all CO2 out of the air in the initial hours of the experiments. The influence of parameters such as PEI loading, adsorption and desorption temperature, particle size, and PEI molecular weight on the adsorption behavior were investigated. The mild regeneration temperatures required could allow the use of waste heat available in many industrial processes as well as solar heat. CO2 adsorption from the air has a number of applications. Removal of CO2 from a closed environment, such as a submarine or space vehicles, is essential for life support. The supply of CO2-free air is also critical for alkaline fuel cells and batteries. Direct air capture of CO2 could also help mitigate the rising concerns about atmospheric CO2 concentration and associated climatic changes, while, at the same time, provide the first step for an anthropogenic carbon cycle. PMID:24644023

  1. Easily Regenerable Solid Adsorbents Based on Polyamines for Carbon Dioxide Capture from the Air

    SciTech Connect

    Goeppert, A; Zhang, H; Czaun, M; May, RB; Prakash, GKS; Olah, GA; Narayanan, SR

    2014-03-18

    Adsorbents prepared easily by impregnation of fumed silica with polyethylenimine (PEI) are promising candidates for the capture of CO2 directly from the air. These inexpensive adsorbents have high CO2 adsorption capacity at ambient temperature and can be regenerated in repeated cycles under mild conditions. Despite the very low CO2 concentration, they are able to scrub efficiently all CO2 out of the air in the initial hours of the experiments. The influence of parameters such as PEI loading, adsorption and desorption temperature, particle size, and PEI molecular weight on the adsorption behavior were investigated. The mild regeneration temperatures required could allow the use of waste heat available in many industrial processes as well as solar heat. CO2 adsorption from the air has a number of applications. Removal of CO2 from a closed environment, such as a submarine or space vehicles, is essential for life support. The supply of CO2-free air is also critical for alkaline fuel cells and batteries. Direct air capture of CO2 could also help mitigate the rising concerns about atmospheric CO2 concentration and associated climatic changes, while, at the same time, provide the first step for an anthropogenic carbon cycle.

  2. Highly selective capture of phosphopeptides using a nano titanium dioxide-multiwalled carbon nanotube nanocomposite.

    PubMed

    Fang, Guozhen; Gao, Wei; Deng, Qiliang; Qian, Kun; Han, Haitao; Wang, Shuo

    2012-04-15

    In this study, a titanium dioxide-multiwalled carbon nanotube (TiO2-MWNT) nanocomposite was first used to enrich phosphopeptides as a binding agent. The TiO2-MWNT nanocomposite was synthesized by the hydrothermal reaction process and characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR), and X-ray powder diffraction (XRD). The results demonstrated that the anatase phase TiO2 nanoparticles had been successfully linked by MWNTs. The TiO2-MWNT nanocomposite was applied as a sorbent to enrich phosphopeptides, and the results showed that the performance of the TiO2-MWNT nanocomposite was better than 5 μm TiO2, as confirmed by the analysis of phosphopeptides from a tryptic digest of a standard protein (β-casein and bovine serum albumin) using high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS). The use of lactic acid in the loading buffer significantly enhances the selectivity of the TiO2-MWNT nanocomposite. This nanocomposite material was further applied to enrich the phosphopeptides in a protein digest obtained from nonfat milk successfully. PMID:22369891

  3. Metal-organic frameworks with precisely designed interior for carbon dioxide capture in the presence of water.

    PubMed

    Fracaroli, Alejandro M; Furukawa, Hiroyasu; Suzuki, Mitsuharu; Dodd, Matthew; Okajima, Satoshi; Gándara, Felipe; Reimer, Jeffrey A; Yaghi, Omar M

    2014-06-25

    The selective capture of carbon dioxide in the presence of water is an outstanding challenge. Here, we show that the interior of IRMOF-74-III can be covalently functionalized with primary amine (IRMOF-74-III-CH2NH2) and used for the selective capture of CO2 in 65% relative humidity. This study encompasses the synthesis, structural characterization, gas adsorption, and CO2 capture properties of variously functionalized IRMOF-74-III compounds (IRMOF-74-III-CH3, -NH2, -CH2NHBoc, -CH2NMeBoc, -CH2NH2, and -CH2NHMe). Cross-polarization magic angle spinning (13)C NMR spectra showed that CO2 binds chemically to IRMOF-74-III-CH2NH2 and -CH2NHMe to make carbamic species. Carbon dioxide isotherms and breakthrough experiments show that IRMOF-74-III-CH2NH2 is especially efficient at taking up CO2 (3.2 mmol of CO2 per gram at 800 Torr) and, more significantly, removing CO2 from wet nitrogen gas streams with breakthrough time of 610 ± 10 s g(-1) and full preservation of the IRMOF structure.

  4. Molecular simulation of carbon dioxide adsorption for carbon capture and storage

    NASA Astrophysics Data System (ADS)

    Tenney, Craig M.

    Capture of CO2 from fossil fuel power plants and sequestration in unmineable coal seams are achievable methods for reducing atmospheric emissions of this greenhouse gas. To aid the development of effective CO2 capture and sequestration technologies, a series of molecular simulation studies were conducted to study the adsorption of CO2 and related species onto heterogeneous, solid adsorbents. To investigate the influence of surface heterogeneity upon adsorption behavior in activated carbons and coal, isotherms were generated via grand canonical Monte Carlo (GCMC) simulation for CO2 adsorption in slit-shaped pores with several variations of chemical and structural heterogeneity. Adsorption generally increased with increasing oxygen content and the presence of holes or furrows, which acted as preferred binding sites. To investigate the potential use of the flexible metal organic framework (MOF) Cu(BF4)2(bpy)2 (bpy=bipyridine) for CO2 capture, pure- and mixed-gas adsorption was simulated at conditions representative of power plant process streams. This MOF was chosen because it displays a novel behavior in which the crystal structure reversibly transitions from an empty, zero porosity state to a saturated, expanded state at the "gate pressure". Estimates of CO2 capacity above the gate pressure from GCMC simulations using a rigid MOF model showed good agreement with experiment. The CO2 adsorption capacity and estimated heats of adsorption are comparable to common physi-adsorbents under similar conditions. Mixed-gas simulations predicted CO2/N2 and CO2/H 2selectivities higher than typical microporous materials. To more closely investigate this gating effect, hybrid Monte-Carlo/molecular-dynamics (MCMD) was used to simulate adsorption using a flexible MOF model. Simulation cell volumes remained relatively constant at low gas pressures before increasing at higher pressure. Mixed-gas simulations predicted CO2/N 2 selectivities comparable to other microporous adsorbents. To

  5. Process for CO2 Capture Using Ionic Liquid That Exhibits Phase Change

    SciTech Connect

    Eisinger, RS; Keller, GE

    2014-11-01

    A novel process for capturing carbon dioxide from the flue gas of a coal-fired power plant has been shown to reduce parasitic power consumption substantially. The process employs an ionic liquid created at the University of Notre Dame that has a high capacity for absorbing CO2 by chemical reaction. A distinguishing property of this ionic liquid is that it changes phase from solid to liquid upon reaction with CO2. The process uses heat generated by this phase transition to lower parasitic power consumption. The driving force for CO2 separation is a combination of temperature and pressure differences; the process could even work without the addition of heat. A realistic process was created to capture CO2 efficiently. Computer simulation of the process enabled calculation of viable process conditions and power usage. The main concepts of the process were shown to work using a lab-scale apparatus. Parasitic power consumes 23% of net power generation, 55% lower than that of the monoethanolamine (MEA) process. However, capital cost is higher. The cost of electricity (COE) is 28% lower than that of the MEA process.

  6. Stellar capture rates for s-process strong component elements.

    NASA Astrophysics Data System (ADS)

    Mutti, P.; Corvi, F.; Athanassopoulos, K.; Beer, H.; Krupchitsky, P.

    The strong component of the s-process is required for the synthesis of the heaviest s-process elements, namely the lead and the bismuth isotopes. The termination of the path occurs via a cyclic process in which nuclei heavier than bismuth decay via alpha emission to isotopes of lead. In this mass region the abundances are strongly influenced by the double magic 208Pb which, having the smallest cross section of all the heavy elements, acts as a bottle-neck in the s-process path. In the framework of a thorough investigation in the atomic mass region around the neutron magic nuclei, the 209Bi and 207Pb capture cross sections were measured with high resolution at the Geel electron linear accelerator. Capture areas were determined for neutron resonances in a wide energy range and the Maxwellian-averaged cross sections were derived as a function of stellar temperature.

  7. Optimization of carbon capture systems using surrogate models of simulated processes.

    SciTech Connect

    Cozad, A.; Chang, Y.; Sahinidis, N.; Miller, D.

    2011-01-01

    With increasing demand placed on power generation plants to reduce carbon dioxide (CO2) emissions, processes to separate and capture CO2 for eventual sequestration are highly sought after. Carbon capture processes impart a parasitic load on the power plants; it is estimated that this would increase the cost of electricity from existing pulverized coal plants anywhere from 71-85 percent [1]. The National Energy and Technology Lab (NETL) is working to lower this to below a 30 percent increase. To reach this goal, work is being done not only to accurately simulate these processes, but also to leverage those accurate and detailed simulations to design optimal carbon capture processes. The major challenges include the lack of accurate algebraic models of the processes, computationally costly simulations, and insufficiently robust simulations. The first challenge bars the use of provable derivative-based optimization algorithms. The latter two can either lead to difficult or impossible direct derivative-free optimization. To overcome these difficulties, we take a more indirect method to solving this problem by, first, generating an accurate set of algebraic surrogate models from the simulation then using derivative-based solvers to optimize the surrogate models. We developed a method that uses derivative-based and derivative-free optimization alongside machine learning and statistical techniques to generate the set of low-complexity surrogate models using data sampled from detailed simulations. The models are validated and improved through the use of derivative-free solvers to adaptively sample new simulation points. The resulting surrogate models can then be used in a superstructure-based process synthesis and solved using derivative-based methods to optimize carbon capture processes.

  8. Application of optical processing for growth of silicon dioxide

    DOEpatents

    Sopori, B.L.

    1997-06-17

    A process for producing a silicon dioxide film on a surface of a silicon substrate is disclosed. The process comprises illuminating a silicon substrate in a substantially pure oxygen atmosphere with a broad spectrum of visible and infrared light at an optical power density of from about 3 watts/cm{sup 2} to about 6 watts/cm{sup 2} for a time period sufficient to produce a silicon dioxide film on the surface of the silicon substrate. An optimum optical power density is about 4 watts/cm{sup 2} for growth of a 100{angstrom}-300{angstrom} film at a resultant temperature of about 400 C. Deep level transient spectroscopy analysis detects no measurable impurities introduced into the silicon substrate during silicon oxide production and shows the interface state density at the SiO{sub 2}/Si interface to be very low. 1 fig.

  9. Application Of Optical Processing For Growth Of Silicon Dioxide

    DOEpatents

    Sopori, Bhushan L.

    1997-06-17

    A process for producing a silicon dioxide film on a surface of a silicon substrate. The process comprises illuminating a silicon substrate in a substantially pure oxygen atmosphere with a broad spectrum of visible and infrared light at an optical power density of from about 3 watts/cm.sup.2 to about 6 watts/cm.sup.2 for a time period sufficient to produce a silicon dioxide film on the surface of the silicon substrate. An optimum optical power density is about 4 watts/cm.sup.2 for growth of a 100.ANG.-300.ANG. film at a resultant temperature of about 400.degree. C. Deep level transient spectroscopy analysis detects no measurable impurities introduced into the silicon substrate during silicon oxide production and shows the interface state density at the SiO.sub.2 /Si interface to be very low.

  10. Two-neutron capture reactions and the r process

    NASA Astrophysics Data System (ADS)

    Bartlett, Amy; Görres, Joachim; Mathews, Grant J.; Otsuki, Kaori; Wiescher, Michael; Frekers, Dieter; Mengoni, Alberto; Tostevin, Jeffrey

    2006-07-01

    Rates for the He4(2n,γ)He6 and He6(α,n)Be9 reactions have been calculated, including both resonant and nonresonant contributions. The sequential two-neutron capture process on He4 has also been reevaluated on the basis of new experimental results. It is shown that a one-step dineutron capture reaction may enhance the sequential two-neutron reaction rate by several orders of magnitude. This opens the possibility that reaction flow through He4(2n,γ)He6(α,n)Be9 may occur in competition with the bottle-neck three-body reactions He4(2α,γ)C12 and the He4(αn,γ)Be9 that initiate the α process and provide seed nuclei for the r process. Here we explore the effect of such dineutron capture on r-process nucleosynthesis. We show that such reactions have little effect on the final abundance and would change only r-process abundances in an extremely neutron-rich low-temperature r process.

  11. System and process for capture of H.sub.2S from gaseous process streams and process for regeneration of the capture agent

    SciTech Connect

    Heldenbrant, David J; Koech, Phillip K; Rainbolt, James E; Bearden, Mark D; Zheng, Feng

    2014-02-18

    A system and process are disclosed for selective removal and recovery of H.sub.2S from a gaseous volume, e.g., from natural gas. Anhydrous organic, sorbents chemically capture H.sub.2S gas to form hydrosulfide salts. Regeneration of the capture solvent involves addition of an anti-solvent that releases the captured H.sub.2S gas from the capture sorbent. The capture sorbent and anti-solvent are reactivated for reuse, e.g., by simple distillation.

  12. Understanding Geochemical Impacts of Carbon Dioxide Leakage from Carbon Capture and Sequestration

    EPA Science Inventory

    US EPA held a technical Geochemical Impact Workshop in Washington, DC on July 10 and 11, 2007 to discuss geological considerations and Area of Review (AoR) issues related to geologic sequestration (GS) of Carbon Dioxide (CO2). Seventy=one (71) representatives of the electric uti...

  13. High-throughput screening of metal-porphyrin-like graphenes for selective capture of carbon dioxide

    PubMed Central

    Bae, Hyeonhu; Park, Minwoo; Jang, Byungryul; Kang, Yura; Park, Jinwoo; Lee, Hosik; Chung, Haegeun; Chung, ChiHye; Hong, Suklyun; Kwon, Yongkyung; Yakobson, Boris I.; Lee, Hoonkyung

    2016-01-01

    Nanostructured materials, such as zeolites and metal-organic frameworks, have been considered to capture CO2. However, their application has been limited largely because they exhibit poor selectivity for flue gases and low capture capacity under low pressures. We perform a high-throughput screening for selective CO2 capture from flue gases by using first principles thermodynamics. We find that elements with empty d orbitals selectively attract CO2 from gaseous mixtures under low CO2 pressures (~10−3 bar) at 300 K and release it at ~450 K. CO2 binding to elements involves hybridization of the metal d orbitals with the CO2 π orbitals and CO2-transition metal complexes were observed in experiments. This result allows us to perform high-throughput screening to discover novel promising CO2 capture materials with empty d orbitals (e.g., Sc– or V–porphyrin-like graphene) and predict their capture performance under various conditions. Moreover, these findings provide physical insights into selective CO2 capture and open a new path to explore CO2 capture materials. PMID:26902156

  14. High-throughput screening of metal-porphyrin-like graphenes for selective capture of carbon dioxide.

    PubMed

    Bae, Hyeonhu; Park, Minwoo; Jang, Byungryul; Kang, Yura; Park, Jinwoo; Lee, Hosik; Chung, Haegeun; Chung, ChiHye; Hong, Suklyun; Kwon, Yongkyung; Yakobson, Boris I; Lee, Hoonkyung

    2016-02-23

    Nanostructured materials, such as zeolites and metal-organic frameworks, have been considered to capture CO2. However, their application has been limited largely because they exhibit poor selectivity for flue gases and low capture capacity under low pressures. We perform a high-throughput screening for selective CO2 capture from flue gases by using first principles thermodynamics. We find that elements with empty d orbitals selectively attract CO2 from gaseous mixtures under low CO2 pressures (~10(-3) bar) at 300 K and release it at ~450 K. CO2 binding to elements involves hybridization of the metal d orbitals with the CO2 π orbitals and CO2-transition metal complexes were observed in experiments. This result allows us to perform high-throughput screening to discover novel promising CO2 capture materials with empty d orbitals (e.g., Sc- or V-porphyrin-like graphene) and predict their capture performance under various conditions. Moreover, these findings provide physical insights into selective CO2 capture and open a new path to explore CO2 capture materials.

  15. Carbon dioxide capture utilizing zeolites synthesized with paper sludge and scrap-glass.

    PubMed

    Espejel-Ayala, F; Corella, R Chora; Pérez, A Morales; Pérez-Hernández, R; Ramírez-Zamora, R M

    2014-12-01

    The present work introduces the study of the CO2 capture process by zeolites synthesized from paper sludge and scrap glass. Zeolites ZSM-5, analcime and wairakite were produced by means of two types of Structure Directing Agents (SDA): tetrapropilamonium (TPA) and ethanol. On the one hand, zeolite ZSM-5 was synthesized using TPA; on the other hand, analcime and wairakite were produced with ethanol. The temperature programmed desorption (TPD) technique was performed for determining the CO2 sorption capacity of these zeolites at two sorption temperatures: 50 and 100 °C. CO2 sorption capacity of zeolite ZSM-5 synthesized at 50 °C was 0.683 mmol/g representing 38.2% of the value measured for a zeolite ZSM-5 commercial. Zeolite analcime showed a higher CO2 sorption capacity (1.698 mmol/g) at 50 °C and its regeneration temperature was relatively low. Zeolites synthesized in this study can be used in the purification of biogas and this will produce energy without increasing the atmospheric CO2 concentrations.

  16. CO₂ Capture Membrane Process for Power Plant Flue Gas

    SciTech Connect

    Toy, Lora; Kataria, Atish; Gupta, Raghubir

    2012-04-01

    Because the fleet of coal-fired power plants is of such importance to the nation's energy production while also being the single largest emitter of CO₂, the development of retrofit, post-combustion CO₂ capture technologies for existing and new, upcoming coal power plants will allow coal to remain a major component of the U.S. energy mix while mitigating global warming. Post-combustion carbon capture technologies are an attractive option for coal-fired power plants as they do not require modification of major power-plant infrastructures, such as fuel processing, boiler, and steam-turbine subsystems. In this project, the overall objective was to develop an advanced, hollow-fiber, polymeric membrane process that could be cost-effectively retrofitted into current pulverized coal-fired power plants to capture at least 90% of the CO₂ from plant flue gas with 95% captured CO₂ purity. The approach for this project tackled the technology development on three different fronts in parallel: membrane materials R&D, hollow-fiber membrane module development, and process development and engineering. The project team consisted of RTI (prime) and two industrial partners, Arkema, Inc. and Generon IGS, Inc. Two CO₂-selective membrane polymer platforms were targeted for development in this project. For the near term, a next-generation, high-flux polycarbonate membrane platform was spun into hollow-fiber membranes that were fabricated into both lab-scale and larger prototype (~2,200 ft²) membrane modules. For the long term, a new fluoropolymer membrane platform based on poly(vinylidene fluoride) [PVDF] chemistry was developed using a copolymer approach as improved capture membrane materials with superior chemical resistance to flue-gas contaminants (moisture, SO₂, NOx, etc.). Specific objectives were: - Development of new, highly chemically resistant, fluorinated polymers as membrane materials with minimum selectivity of 30 for CO₂ over N₂ and CO₂ permeance

  17. Neutron Induced Capture and Fission Processes on 238U

    NASA Astrophysics Data System (ADS)

    Oprea, Cristiana; Oprea, Alexandru

    2016-03-01

    Nuclear data on Uranium isotopes are of crucial interest for new generation of nuclear reactors. Processes of interest are the nuclear reactions induced by neutrons and in this work mainly the capture and the fission process on 238U will be analyzed in a wide energy interval. For slow and resonant neutrons the many levels Breit - Wigner formalism is necessary. In the case of fast and very fast neutrons up to 200 MeV the nuclear reaction mechanism implemented in Talys will be used. The present evaluations are necessary in order to obtain the field of neutrons in the design of nuclear reactors and they are compared with experimental data from literature obtained from capture and (n,xn) processes.

  18. Synthesis, structure, and carbon dioxide capture properties of zeolitic imidazolate frameworks.

    PubMed

    Phan, Anh; Doonan, Christian J; Uribe-Romo, Fernando J; Knobler, Carolyn B; O'Keeffe, Michael; Yaghi, Omar M

    2010-01-19

    capture of CO(2) and its selective separation from industrially relevant gas mixtures. Currently, ZIFs are the best porous materials for the selective capture of CO(2); furthermore, they show exceptionally high capacity for CO(2) among adsorbents operating by physisorption. The stability of ZIFs has also enabled organic transformations to be carried out on the crystals, yielding covalently functionalized isoreticular structures wherein the topology, crystallinity, and porosity of the ZIF structure are maintained throughout the reaction process. These reactions, being carried out on macroscopic crystals that behave as single molecules, have enabled the realization of the chemist's dream of using "crystals as molecules", opening the way for the application of the extensive library of organic reactions to the functionalization of useful extended porous structures. PMID:19877580

  19. Synthesis, structure, and carbon dioxide capture properties of zeolitic imidazolate frameworks.

    PubMed

    Phan, Anh; Doonan, Christian J; Uribe-Romo, Fernando J; Knobler, Carolyn B; O'Keeffe, Michael; Yaghi, Omar M

    2010-01-19

    capture of CO(2) and its selective separation from industrially relevant gas mixtures. Currently, ZIFs are the best porous materials for the selective capture of CO(2); furthermore, they show exceptionally high capacity for CO(2) among adsorbents operating by physisorption. The stability of ZIFs has also enabled organic transformations to be carried out on the crystals, yielding covalently functionalized isoreticular structures wherein the topology, crystallinity, and porosity of the ZIF structure are maintained throughout the reaction process. These reactions, being carried out on macroscopic crystals that behave as single molecules, have enabled the realization of the chemist's dream of using "crystals as molecules", opening the way for the application of the extensive library of organic reactions to the functionalization of useful extended porous structures.

  20. Redox processes in silicon dioxide thin films using copper microelectrodes

    NASA Astrophysics Data System (ADS)

    Tappertzhofen, S.; Menzel, S.; Valov, I.; Waser, R.

    2011-11-01

    Although SiO2 is a typical insulator, we demonstrate an electrochemical characteristic of the Cu/Cu+ oxidation at the interface with 30 nm thick silicon dioxide thin films studied by cyclic voltammetry. This study reveals the process of anodic oxidation and subsequent reduction of oxidized Cu ions injected in the SiO2 layer with special attention to the kinetics of the redox process. We estimated the diffusion coefficient and the mobility of Cu ions in SiO2. The results gain deeper insight in the processes involved during resistive switching of Cu/SiO2 based nonvolatile memory devices.

  1. Capturing, processing, and rendering real-world scenes

    NASA Astrophysics Data System (ADS)

    Nyland, Lars S.; Lastra, Anselmo A.; McAllister, David K.; Popescu, Voicu; McCue, Chris; Fuchs, Henry

    2000-12-01

    While photographs vividly capture a scene from a single viewpoint, it is our goal to capture a scene in such a way that a viewer can freely move to any viewpoint, just as he or she would in an actual scene. We have built a prototype system to quickly digitize a scene using a laser rangefinder and a high-resolution digital camera that accurately captures a panorama of high-resolution range and color information. With real-world scenes, we have provided data to fuel research in many area, including representation, registration, data fusion, polygonization, rendering, simplification, and reillumination. The real-world scene data can be used for many purposes, including immersive environments, immersive training, re-engineering and engineering verification, renovation, crime-scene and accident capture and reconstruction, archaeology and historic preservation, sports and entertainment, surveillance, remote tourism and remote sales. We will describe our acquisition system, the necessary processing to merge data from the multiple input devices and positions. We will also describe high quality rendering using the data we have collected. Issues about specific rendering accelerators and algorithms will also be presented. We will conclude by describing future uses and methods of collection for real- world scene data.

  2. Dissolution rate measurements for resist processing in supercritical carbon dioxide

    NASA Astrophysics Data System (ADS)

    Pham, Victor Q.; Weibel, Gina L.; Rao, Nagesh G.; Ober, Christopher K.

    2002-07-01

    A dissolution rate monitor (DRM) was successfully constructed to study the behavior of thin photoresist films undergoing the dissolution process in supercritical carbon dioxide (SCCO2). The DRM is based on the principles of interferometry but requires special modifications to the processing vessel to allow for the passage of transmitted and reflected He-Ne laser light. Dissolution rates obtained agree well with independent profilometric measurements of film thickness loss. We found that for block and random copolymers of THPMA-F7MA, dissolution rates vary with film thickness, slowing down considerably towards the silicon surface. This behavior was also observed in TBMA-F7MA random copolymers.

  3. System and process for capture of acid gasses at elevated pressure from gaseous process streams

    DOEpatents

    Heldebrant, David J.; Koech, Phillip K.; Linehan, John C.; Rainbolt, James E.; Bearden, Mark D.; Zheng, Feng

    2016-09-06

    A system, method, and material that enables the pressure-activated reversible chemical capture of acid gasses such as CO.sub.2 from gas volumes such as streams, flows or any other volume. Once the acid gas is chemically captured, the resulting product typically a zwitterionic salt, can be subjected to a reduced pressure whereupon the resulting product will release the captures acid gas and the capture material will be regenerated. The invention includes this process as well as the materials and systems for carrying out and enabling this process.

  4. Nanoclay-Based Solid-Amine Adsorbents for Carbon Dioxide Capture

    NASA Astrophysics Data System (ADS)

    Roth, Elliot A.

    The objective of this research was to develop an efficient, low cost, recyclable solid sorbent for carbon dioxide adsorption from large point sources, such as coal-fired power plants. The current commercial way to adsorb CO 2 is to use a liquid amine or ammonia process. These processes are used in industry in the "sweetening" of natural gas, but liquid based technologies are not economically viable in the adsorption of CO2 from power plants due to the extremely large volume of CO2 and the inherent high regeneration costs of cycling the sorbent. Therefore, one of the main objectives of this research was to develop a novel sorbent that can be cycled and uses very little energy for regeneration. The sorbent developed here is composed of a nanoclay (montmorillonite), commonly used in the production of polymer nanocomposites, grafted with commercially available amines. (3-aminopropyl) trimethoxysilane (APTMS) was chemically grafted to the edge hydroxyl groups of the clay. While another amine, polyethylenimine (PEI), was attached to the surface of the clay by electrostatic interactions. To confirm the attachment of amines to the clay, the samples were characterized using FTIR and the corresponding peaks for amines were observed. The amount of amine loaded onto the support was determined by TGA techniques. The treated clay was initially analyzed for CO2 adsorption in a pure CO 2 stream. The adsorption temperatures that had the highest adsorption capacity were determined to be between 75°C and 100°C for all of the samples tested at atmospheric pressure. The maximum CO2 adsorption capacity observed was with nanoclay treated with both APTMS and PEI at 85°C. In a more realistic flue gas of 10% CO2 and 90% N2, the adsorbents had essentially the same overall CO2 adsorption capacity indicating that the presence of nitrogen did not hinder the adsorption of CO2. Adsorption studies in pure CO2 at room temperature under pressure from 40-300 PSI were also conducted. The average

  5. Synthesis, Structure, and Carbon Dioxide Capture Properties of Zeolitic Imidazolate Frameworks

    SciTech Connect

    Phan, Anh; Doonan, Christian J.; Uribe-Romo, Fernando J.; Knobler, Carolyn B.; O’Keeffe, Michael; Yaghi, Omar M.

    2010-01-19

    capture of CO2 and its selective separation from industrially relevant gas mixtures. Currently, ZIFs are the best porous materials for the selective capture of CO2; furthermore, they show exceptionally high capacity for CO2 among adsorbents operating by physisorption. The stability of ZIFs has also enabled organic transformations to be carried out on the crystals, yielding covalently functionalized isoreticular structures wherein the topology, crystallinity, and porosity of the ZIF structure are maintained throughout the reaction process. Finally, these reactions, being carried out on macroscopic crystals that behave as single molecules, have enabled the realization of the chemist’s dream of using “crystals as molecules”, opening the way for the application of the extensive library of organic reactions to the functionalization of useful extended porous structures.

  6. Post-combustion Carbon Dioxide Capture using Amine Functionalized Solid Sorbents

    NASA Astrophysics Data System (ADS)

    Mittal, Nikhil

    This work is divided into two parts: (1) Synthesis of amine functionalized adsorbents using grafting technique for post-combustion CO2 capture, (2) Performance evaluation of structured bed configuration with straight gas flow channels using amine impregnated adsorbent for post-combustion CO 2 capture. Brief description of each part is given below: (1) N-(3-trimethoxysilylpropyl)diethylenetriamine (DAEAPTS) grafted SBA-15 adsorbents were synthesized for CO2 capture. The adsorption of CO2 on the amine-grafted sorbents was measured by thermogravimetric method over a CO2 partial pressure range of 8--101.3 kPa and a temperature range of 25--105 °C under atmospheric pressure. The optimal amine loaded SBA-15 adsorbent was examined for multi-cycle stability and adsorption/desorption kinetics. (2) The performance of structured bed and packed bed configurations for post-combustion CO2 capture was evaluated using PEI impregnated SBA-15 adsorbent. The effect of adsorption temperature (25-90 °C), adsorption /desorption kinetics and multi-cycle stability was studied in both structured and packed bed configurations.

  7. Carbon capture by sorption-enhanced water-gas shift reaction process using hydrotalcite-based material

    SciTech Connect

    van Selow, E.R.; Cobden, P.D.; Verbraeken, P.A.; Hufton, J.R.; van den Brink, R.W.

    2009-05-15

    A novel route for precombustion decarbonization is the sorption-enhanced water-gas shift (SEWGS) process. In this process carbon dioxide is removed from a synthesis gas at elevated temperature by adsorption. Simultaneously, carbon monoxide is converted to carbon dioxide by the water-gas shift reaction. The periodic adsorption and desorption of carbon dioxide is induced by a pressure swing cycle, and the cyclic capacity can be amplified by purging with steam. From previous studies is it known that for SEWGS applications, hydrotalcite-based materials are particularly attractive as sorbent, and commercial high-temperature shift catalysts can be used for the conversion of carbon monoxide. Tablets of a potassium promoted hydrotalcite-based material are characterized in both breakthrough and cyclic experiments in a 2 m tall fixed-bed reactor. When exposed to a mixture of carbon dioxide, steam, and nitrogen at 400{sup o}C, the material shows a breakthrough capacity of 1.4 mmol/g. In subsequent experiments the material was mixed with tablets of promoted iron-chromium shift catalyst and exposed to a mixture of carbon dioxide, carbon monoxide, steam, hydrogen, and nitrogen. It is demonstrated that carbon monoxide conversion can be enhanced to 100% in the presence of a carbon dioxide sorbent. At breakthrough, carbon monoxide and carbon dioxide simultaneously appear at the end of the bed. During more than 300 cycles of adsorption/reaction and desorption, the capture rate, and carbon monoxide conversion are confirmed to be stable. Two different cycle types are investigated: one cycle with a CO{sub 2} rinse step and one cycle with a steam rinse step. The performance of both SEWGS cycles are discussed.

  8. Computational Tools for Accelerating Carbon Capture Process Development

    SciTech Connect

    Miller, David

    2013-01-01

    The goals of the work reported are: to develop new computational tools and models to enable industry to more rapidly develop and deploy new advanced energy technologies; to demonstrate the capabilities of the CCSI Toolset on non-proprietary case studies; and to deploy the CCSI Toolset to industry. Challenges of simulating carbon capture (and other) processes include: dealing with multiple scales (particle, device, and whole process scales); integration across scales; verification, validation, and uncertainty; and decision support. The tools cover: risk analysis and decision making; validated, high-fidelity CFD; high-resolution filtered sub-models; process design and optimization tools; advanced process control and dynamics; process models; basic data sub-models; and cross-cutting integration tools.

  9. An economic analysis of the Jim Bridger Power Plant carbon dioxide mineralization process

    NASA Astrophysics Data System (ADS)

    Christensen, Mikol Hans

    Concerns for rising levels of CO2 in the atmosphere have lead to a myriad of schemes to reduce emissions. Many of these are complicated, expensive, and untried. Coal-fired electrical generation accounts for about 49 percent of U.S. electricity generation. Shifting generation capacity away from coal is the goal of many, yet as this statistic shows, the U.S. has a heavy dependency on coal-fired base-load generation. What is needed is a way to retrofit existing coal fired power plants to mitigate at least some of the giga-tonnes of CO2 released annually. Carbon Capture and Storage in association with greenhouse gases are a major concern in the world today. This thesis is an outgrowth of a research partnership between the University of Wyoming and the Jim Bridger Power Plant (Rocky Mountain Power) to develop a process for capture and mineralization of flue gas carbon dioxide (CO 2) using an accelerated mineral carbonization process with fly ash particles as the absorbent. This process may have several advantages over other approaches because it is an environmentally acceptable, single step process occurring at near ambient pressures and temperatures that can compliment conventional CCS processes. In addition the use of fly ash particles as an absorbent avoids the costs of processing or engineering an absorbent. The purpose of this thesis is to evaluate the capture costs and economic feasibility of the mineralization process. Two models were used to estimate the capture costs and economic feasibility of the Jim Bridger Power Plant CO2 Mineralization Project (JBP). The first was a cost of capture model which was used to estimate CO2 capture costs and how changes in the CO2 to ash capture ratio and quantities of CO2 captured affect capture costs. The second was a financial feasibility model which considered the time value of money. This second model considered the net present value (NPV) and internal rate of return (IRR) for the process using different pricing scenarios

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

    PubMed

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

    2016-09-01

    Greenhouse gas emissions have several adverse environmental effects, like pollution and climate change. Currently applied carbon capture and storage (CCS) methods are not cost effective and have not been proven safe for long term sequestration. Another attractive approach is CO2 valorization, whereby CO2 can be captured in the form of biomass via photosynthesis and is subsequently converted into various form of bioenergy. This article summarizes the current carbon sequestration and utilization technologies, while emphasizing the value of bioconversion of CO2. In particular, CO2 sequestration by terrestrial plants, microalgae and other microorganisms are discussed. Prospects and challenges for CO2 conversion are addressed. The aim of this review is to provide comprehensive knowledge and updated information on the current advances in biological CO2 sequestration and valorization, which are essential if this approach is to achieve environmental sustainability and economic feasibility. PMID:27090405

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

    PubMed

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

    2016-09-01

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

  12. Membrane Process to Capture CO{sub 2} from Coal-Fired Power Plant Flue Gas

    SciTech Connect

    Merkel, Tim; Wei, Xiaotong; Firat, Bilgen; He, Jenny; Amo, Karl; Pande, Saurabh; Baker, Richard; Wijmans, Hans; Bhown, Abhoyjit

    2012-03-31

    This final report describes work conducted for the U.S. Department of Energy National Energy Technology Laboratory (DOE NETL) on development of an efficient membrane process to capture carbon dioxide (CO{sub 2}) from power plant flue gas (award number DE-NT0005312). The primary goal of this research program was to demonstrate, in a field test, the ability of a membrane process to capture up to 90% of CO{sub 2} in coal-fired flue gas, and to evaluate the potential of a full-scale version of the process to perform this separation with less than a 35% increase in the levelized cost of electricity (LCOE). Membrane Technology and Research (MTR) conducted this project in collaboration with Arizona Public Services (APS), who hosted a membrane field test at their Cholla coal-fired power plant, and the Electric Power Research Institute (EPRI) and WorleyParsons (WP), who performed a comparative cost analysis of the proposed membrane CO{sub 2} capture process. The work conducted for this project included membrane and module development, slipstream testing of commercial-sized modules with natural gas and coal-fired flue gas, process design optimization, and a detailed systems and cost analysis of a membrane retrofit to a commercial power plant. The Polaris? membrane developed over a number of years by MTR represents a step-change improvement in CO{sub 2} permeance compared to previous commercial CO{sub 2}-selective membranes. During this project, membrane optimization work resulted in a further doubling of the CO{sub 2} permeance of Polaris membrane while maintaining the CO{sub 2}/N{sub 2} selectivity. This is an important accomplishment because increased CO{sub 2} permeance directly impacts the membrane skid cost and footprint: a doubling of CO{sub 2} permeance halves the skid cost and footprint. In addition to providing high CO{sub 2} permeance, flue gas CO{sub 2} capture membranes must be stable in the presence of contaminants including SO{sub 2}. Laboratory tests showed no

  13. Rate-based process modeling study of CO{sub 2} capture with aqueous monoethanolamine solution

    SciTech Connect

    Zhang, Y.; Chen, H.; Chen, C.C.; Plaza, J.M.; Dugas, R.; Rochelle, G.T.

    2009-10-15

    Rate-based process modeling technology has matured and is increasingly gaining acceptance over traditional equilibrium-stage modeling approaches. Recently comprehensive pilot plant data for carbon dioxide (CO{sub 2}) capture with aqueous monoethanolamine (MEA) solution have become available from the University of Texas at Austin. The pilot plant data cover key process variables including CO{sub 2} concentration in the gas stream, CO{sub 2} loading in lean MEA solution, liquid to gas ratio, and packing type. In this study, we model the pilot plant operation with Aspen RateSep, a second generation rate-based multistage separation unit operation model in Aspen Plus. After a brief review of rate-based modeling, thermodynamic and kinetic models for CO{sub 2} absorption with the MEA solution, and transport property models, we show excellent match of the rate-based model predictions against the comprehensive pilot plant data and we validate the superiority of the rate-based models over the traditional equilibrium-stage models. We further examine the impacts of key rate-based modeling options, i.e., film discretization options and flow model options. The rate-based model provides excellent predictive capability, and it should be very useful for design and scale-up of CO{sub 2} capture processes.

  14. Carbon dioxide capture-related gas adsorption and separation in metal-organic frameworks

    SciTech Connect

    Li, JR; Ma, YG; McCarthy, MC; Sculley, J; Yu, JM; Jeong, HK; Balbuena, PB; Zhou, HC

    2011-08-01

    Reducing anthropogenic CO2 emission and lowering the concentration of greenhouse gases in the atmosphere has quickly become one of the most urgent environmental issues of our age. Carbon capture and storage (CCS) is one option for reducing these harmful CO2 emissions. While a variety of technologies and methods have been developed, the separation of CO2 from gas streams is still a critical issue. Apart from establishing new techniques, the exploration of capture materials with high separation performance and low capital cost are of paramount importance. Metal-organic frameworks (MOFs), a new class of crystalline porous materials constructed by metal-containing nodes bonded to organic bridging ligands hold great potential as adsorbents or membrane materials in gas separation. In this paper, we review the research progress (from experimental results to molecular simulations) in MOFs for CO2 adsorption, storage, and separations (adsorptive separation and membrane-based separation) that are directly related to CO2 capture. (C) 2011 Elsevier B.V. All rights reserved.

  15. Carbon dioxide capture using Escherichia coli expressing carbonic anhydrase in a foam bioreactor.

    PubMed

    Watson, Stuart K; Han, Zhenlin; Su, Wei Wen; Deshusses, Marc A; Kan, Eunsung

    2016-12-01

    The present study reports CO2 capture and conversion to bicarbonate using Escherichia coli expressing carbonic anhydrase (CA) on its cell surface in a novel foam bioreactor. The very large gas-liquid interfacial area in the foam bioreactor promoted rapid CO2 absorption while the CO2 in the aqueous phase was subsequently converted to bicarbonate ions by the CA. CO2 gas removal in air was investigated at various conditions such as gas velocity, cell density and CO2 inlet concentration. Regimes for kinetic and mass transfer limitations were defined. Very high removal rates of CO2 were observed: 9570 g CO2 m(-3) bioreactor h(-1) and a CO2 removal efficiency of 93% at 4% inlet CO2 when the gas retention time was 24 s, and cell concentration was 4 gdw L(-1). These performances are superior to earlier reports of experimental bioreactors using CA for CO2 capture. Overall, this bioreactor system has significant potential as an alternative CO2 capture technology.

  16. Recent advances in carbon dioxide capture, fixation, and activation by using N-heterocyclic carbenes.

    PubMed

    Yang, Longhua; Wang, Hongming

    2014-04-01

    In the last two decades, CO2 emission has caused a lot of environmental problems. To mitigate the concentration of CO2 in the atmosphere, various strategies have been implemented, one of which is the use of N-heterocyclic carbenes (NHCs) and related complexes to accomplish the capture, fixation, and activation of CO2 effectively. In this review, we summarize CO2 capture, fixation, and activation by utilizing NHCs and related complexes; homogeneous reactions and their reaction mechanisms are discussed. Free NHCs and NHC salts can capture CO2 in both direct and indirect ways to form imidazolium carboxylates, and they can also catalyze the reaction of aromatic aldehydes with CO2 to form carboxylic acids and derivatives. Moreover, associated with transition metals (TMs), NHCs can form NHC-TM complexes to transform CO2 into industrial acid or esters. Non-metal-NHC complexes can also catalyze the reactions of silicon and boron complexes with CO2 . In addition, catalytic cycloaddition of epoxides with CO2 is another effective function of NHC complexes, and NHC ionic liquids perform excellently in this aspect.

  17. A new class of single-component absorbents for reversible carbon dioxide capture under mild conditions.

    PubMed

    Barzagli, Francesco; Lai, Sarah; Mani, Fabrizio

    2015-01-01

    Some inexpensive and commercially available secondary amines reversibly react with CO2 at room temperature and ambient pressure to yield carbonated species in the liquid phase in the absence of any additional solvent. These solvent-free absorbents have a high CO2 capture capacity (0.63-0.65 mol CO2 /mol amine) at 1.0 bar (=100 kPa), combined with low-temperature reversibility at ambient pressure. (13) C NMR spectroscopy analysis identified the carbonated species as the carbamate salts and unexpected carbamic acids. These absorbents were used for CO2 (15 and 40 % in air) capture in continuous cycles of absorption-desorption carried out in packed columns, yielding an absorption efficiency of up to 98.5 % at absorption temperatures of 40-45 °C and desorption temperatures of 70-85 °C at ambient pressure. The absence of any parasitic solvent that requires to be heated and stability towards moisture and heating could result in some of these solvent-free absorbents being a viable alternative to aqueous amines for CO2 chemical capture.

  18. Bacterial Synthesis of Unusual Sulfonamide and Sulfone Antibiotics by Flavoenzyme-Mediated Sulfur Dioxide Capture.

    PubMed

    Baunach, Martin; Ding, Ling; Willing, Karsten; Hertweck, Christian

    2015-11-01

    Sulfa drugs, such as sulfonilamide and dapsone, are classical antibiotics that have been in clinical use worldwide. Despite the relatively simple architectures, practically no natural products are known to feature such aromatic sulfonamide or diarylsulfone substructures. We report the unexpected discovery of three fully unprecedented, sulfonyl-bridged alkaloid dimers (sulfadixiamycins A-C) from recombinant Streptomyces species harboring the entire xiamycin biosynthesis gene cluster. Sulfadixiamycins exhibit moderate antimycobacterial activities and potent antibiotic activities even against multidrug-resistant bacteria. Gene inactivation, complementation, and biotransformation experiments revealed that a flavin-dependent enzyme (XiaH) plays a key role in sulfadixiamycin biosynthesis. XiaH mediates a radical-based, three-component reaction involving two equivalents of xiamycin and sulfur dioxide, which is reminiscent of radical styrene/SO2 copolymerization. PMID:26366473

  19. Ambient carbon dioxide capture by different dimensional AlN nanostructures: A comparative DFT study

    NASA Astrophysics Data System (ADS)

    Esrafili, Mehdi D.; Nurazar, Roghaye; Nematollahi, Parisa

    2016-08-01

    Strong binding of an isolated carbon dioxide molecule over three different aluminium nitride (AlN) nanostructures (nanocage, nanotube and nanosheet) is verified using density functional calculations. Equilibrium geometries, electronic properties, adsorption energies and thermodynamic stability of each adsorbed configuration are also identified. Optimized configurations are shown at least one corresponding physisorption and chemisorption of CO2 molecule over different AlN nanostructures. Also, the effect of chirality on the adsorption of CO2 molecule is studied over two different finite-sized zigzag (6,0) and armchair (4,4) AlN nanotubes. It is found that the electronic properties of the Al12N12 nanocage are more sensitive to the CO2 molecule than other AlN nanostructures. This indicates the significant potential of Al12N12 nanocage toward the CO2 adsorption, fixation and catalytic applications in contrast to other AlN nanostructures.

  20. Carbon dioxide capture on amine-rich carbonaceous materials derived from glucose.

    PubMed

    Zhao, Li; Bacsik, Zoltan; Hedin, Niklas; Wei, Wei; Sun, Yuhan; Antonietti, Markus; Titirici, Maria-Magdalena

    2010-07-19

    The synthesis of carbonaceous materials with a high surface density of amino functions for CO(2) sorption and sequestration is reported. The amino-rich carbonaceous materials are characterized by elemental analysis, N(2) sorption, scanning and transmission electron microscopy, zeta potential, TGA and FTIR measurements. A detailed discussion on the use of these materials in CO(2) capture is provided. The materials show significant sorption capabilities for CO(2) (4.3 mmol g(-1)at -20 degrees C and 1 bar). Furthermore, they show a high apparent selectivity for CO(2) over N(2) at both low and high temperatures.

  1. Evaluation of cation-exchanged zeolite adsorbents for post-combustion carbon dioxide capture

    SciTech Connect

    Bae, TH; Hudson, MR; Mason, JA; Queen, WL; Dutton, JJ; Sumida, K; Micklash, KJ; Kaye, SS; Brown, CM; Long, JR

    2013-01-01

    A series of zeolite adsorbents has been evaluated for potential application in post-combustion CO2 capture using a new high-throughput gas adsorption instrument capable of measuring 28 samples in parallel. Among the zeolites tested, Ca-A exhibits the highest CO2 uptake (3.72 mmol g(-1) and 5.63 mmol cm(-3)) together with an excellent CO2 selectivity over N-2 under conditions relevant to capture from the dry flue gas stream of a coal-fired power plant. The large initial isosteric heat of adsorption of -58 kJ mol(-1) indicates the presence of strong interactions between CO2 and the Ca-A framework. Neutron and X-ray powder diffraction studies reveal the precise location of the adsorption sites for CO2 in Ca-A and Mg-A. A detailed study of CO2 adsorption kinetics further shows that the performance of Ca-A is not limited by slow CO2 diffusion within the pores. Significantly, Ca-A exhibited a higher volumetric CO2 uptake and CO2/N-2 selectivity than Mg-2(dobdc) (dobdc(4-) = 1,4-dioxido-2,5-benzenedicarboxylate; Mg-MOF-74, CPO-27-Mg), one of the best performing adsorbents. The exceptional performance of Ca-A was maintained in CO2 breakthrough simulations.

  2. Effects of carbonization parameters of Moso-bamboo-based porous charcoal on capturing carbon dioxide.

    PubMed

    Huang, Pei-Hsing; Jhan, Jhih-Wei; Cheng, Yi-Ming; Cheng, Hau-Hsein

    2014-01-01

    This study experimentally analyzed the carbon dioxide adsorption capacity of Moso-bamboo- (Phyllostachys edulis-) based porous charcoal. The porous charcoal was prepared at various carbonization temperatures and ground into powders with 60, 100, and 170 meshes, respectively. In order to understand the adsorption characteristics of porous charcoal, its fundamental properties, namely, charcoal yield, ash content, pH value, Brunauer-Emmett-Teller (BET) surface area, iodine number, pore volume, and powder size, were analyzed. The results show that when the carbonization temperature was increased, the charcoal yield decreased and the pH value increased. Moreover, the bamboo carbonized at a temperature of 1000(°)C for 2 h had the highest iodine sorption value and BET surface area. In the experiments, charcoal powders prepared at various carbonization temperatures were used to adsorb 1.854% CO2 for 120 h. The results show that the bamboo charcoal carbonized at 1000(°)C and ground with a 170 mesh had the best adsorpt on capacity, significantly decreasing the CO2 concentration to 0.836%. At room temperature and atmospheric pressure, the Moso-bamboo-based porous charcoal exhibited much better CO2 adsorption capacity compared to that of commercially available 350-mesh activated carbon.

  3. Effects of Carbonization Parameters of Moso-Bamboo-Based Porous Charcoal on Capturing Carbon Dioxide

    PubMed Central

    Jhan, Jhih-Wei; Cheng, Yi-Ming; Cheng, Hau-Hsein

    2014-01-01

    This study experimentally analyzed the carbon dioxide adsorption capacity of Moso-bamboo- (Phyllostachys edulis-) based porous charcoal. The porous charcoal was prepared at various carbonization temperatures and ground into powders with 60, 100, and 170 meshes, respectively. In order to understand the adsorption characteristics of porous charcoal, its fundamental properties, namely, charcoal yield, ash content, pH value, Brunauer-Emmett-Teller (BET) surface area, iodine number, pore volume, and powder size, were analyzed. The results show that when the carbonization temperature was increased, the charcoal yield decreased and the pH value increased. Moreover, the bamboo carbonized at a temperature of 1000°C for 2 h had the highest iodine sorption value and BET surface area. In the experiments, charcoal powders prepared at various carbonization temperatures were used to adsorb 1.854% CO2 for 120 h. The results show that the bamboo charcoal carbonized at 1000°C and ground with a 170 mesh had the best adsorption capacity, significantly decreasing the CO2 concentration to 0.836%. At room temperature and atmospheric pressure, the Moso-bamboo-based porous charcoal exhibited much better CO2 adsorption capacity compared to that of commercially available 350-mesh activated carbon. PMID:25225639

  4. Equilibrium and kinetics analysis of carbon dioxide capture using immobilized amine on a mesoporous silica

    SciTech Connect

    Monazam, E., Shadle, L., Pennline, H., Miller, D., Fauth, D., Hoffman, J., Gray, M.

    2012-01-01

    The equilibrium and conversion-time data on the absorption of carbon dioxide (CO{sub 2}) with amine-based solid sorbent were analyzed over the range of 303–373 K. Data on CO{sub 2} loading on amine based solid sorbent at these temperatures and CO{sub 2} partial pressure between 10 and 760 mm Hg obtained from volumetric adsorption apparatus were fitted to a simple equilibrium model to generate the different parameters (including equilibrium constant) in the model. Using these constants, a correlation was obtained to define equilibrium constant and maximum CO{sub 2} loading as a function of temperature. In this study, a shrinking core model (SCM) was applied to elucidate the relative importance of pore diffusion and surface chemical reaction in controlling the rate of reaction. Application of SCM to the data suggested a surface reaction-controlled mechanism for the temperature of up to 40°C and pore-diffusion mechanism at higher temperature.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  6. Carbon Dioxide Capture and Dyes Separation in a Porous Framework with Anionic Sql Net

    NASA Astrophysics Data System (ADS)

    Tan, Yanxi; Zhang, Ying; Zhang, Jian; Zheng, Yanjun

    2014-12-01

    Presented here is a water-stable MOF material [In(5-AIPA)2] ṡ Me2NH2(1; 5-AIPA = 5-Aminoisophthalic acid) built from the connecting of tetrahedral building units [In(COO)4]-. The sql net of compound 1 exhibits preferable chemical and thermal stability confirmed by thermal gravimetric analyses (TGA) and powder X-ray diffraction pattern (PXRD) measurements. The activated empty phase of 1a, as a good candidate material for CO2 capture, shows a CO2 uptake of 56.6 cm3/g and CH4/CO2 selectivity in excess of 16.4. Remarkably, based on the cation exchange mechanism, 1a has excellent MB affinity and can adsorb MB over MO from water in two hours. The results further support the idea that the ionic MOFs can find more applications in the separation of ionic dyes for the purifying of dye wastewater.

  7. Design of poly(ether block amide)/polyacrylonitrile composite membrane for carbon dioxide capture

    NASA Astrophysics Data System (ADS)

    Wang, Lianjun; Ji, Pengfei; Li, Yang; di, Mingming; Lv, Quan; Li, Shuguang

    2015-03-01

    In this study, poly(ether block amide) was used as coating material to develop a novel composite polymer membrane for CO2 capture. Polyacrylonitrile (PAN) ultrafiltration membrane was applied as substrate. Between them, a gutter layer prepared from cross-linked polydimethylsiloxane (PDMS) blending with amino silicone was introduced to improve separation performance of the composite membrane. The separation properties of resultant triple layer composite membrane was characterized using pure CO2 and N2 gases. It was found that the crosslinking degree of the gutter layer had great influence on membrane performance, which could be significantly improved with the help of amino-PDMS gutter layer compared with that of the membrane having Pebax coating directly onto PAN substrate. Using 2 wt.% Pebax coating solution and properly cross-linked gutter layer, the designed Pebax/amino-PDMS/PAN composite membrane showed CO2 permeance of 147 GPU and CO2/N2 selectivity of 62.

  8. Parallel Processing of Large Scale Microphone Arrays for Sound Capture

    NASA Astrophysics Data System (ADS)

    Jan, Ea-Ee.

    1995-01-01

    Performance of microphone sound pick up is degraded by deleterious properties of the acoustic environment, such as multipath distortion (reverberation) and ambient noise. The degradation becomes more prominent in a teleconferencing environment in which the microphone is positioned far away from the speaker. Besides, the ideal teleconference should feel as easy and natural as face-to-face communication with another person. This suggests hands-free sound capture with no tether or encumbrance by hand-held or body-worn sound equipment. Microphone arrays for this application represent an appropriate approach. This research develops new microphone array and signal processing techniques for high quality hands-free sound capture in noisy, reverberant enclosures. The new techniques combine matched-filtering of individual sensors and parallel processing to provide acute spatial volume selectivity which is capable of mitigating the deleterious effects of noise interference and multipath distortion. The new method outperforms traditional delay-and-sum beamformers which provide only directional spatial selectivity. The research additionally explores truncated matched-filtering and random distribution of transducers to reduce complexity and improve sound capture quality. All designs are first established by computer simulation of array performance in reverberant enclosures. The simulation is achieved by a room model which can efficiently calculate the acoustic multipath in a rectangular enclosure up to a prescribed order of images. It also calculates the incident angle of the arriving signal. Experimental arrays were constructed and their performance was measured in real rooms. Real room data were collected in a hard-walled laboratory and a controllable variable acoustics enclosure of similar size, approximately 6 x 6 x 3 m. An extensive speech database was also collected in these two enclosures for future research on microphone arrays. The simulation results are shown to be

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

    NASA Astrophysics Data System (ADS)

    Johnson, Timothy Lawrence

    2002-09-01

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

  10. Microbial carbon capture cell using cyanobacteria for simultaneous power generation, carbon dioxide sequestration and wastewater treatment.

    PubMed

    Pandit, Soumya; Nayak, Bikram Kumar; Das, Debabrata

    2012-03-01

    Microbial carbon capture cells (MCCs) were constructed with cyanobacteria growing in a photo biocathode in dual-chambered flat plate mediator-less MFCs separated by an anion exchange membrane from the anode compartment containing Shewanella putrefaciens. The performance of the MCC with Anabaena sparged with CO(2)-air mixture was compared with that of a conventional cathode sparged with air only. The power densities achieved were 57.8 mW/m(2) for Anabaena sparged with a CO(2)-air mixture, 39.2 mW/m(2) for CO(2)-air mixture sparging only, 29.7 mW/m(2) for Anabaena sparged with air, and 19.6 mW/m(2) for air sparging only. The pH of the cathode containing Anabaena gradually increased from 7 to 9.12 and power generation decreased from 34.7 to 23.8 mW/m(2) 17 due to pH imbalance associated voltage losses without CO(2)-air mixture sparging. Sparging with a 5% CO(2)-air mixture produced maximum power of 100.1 mW/m(2). In addition, the power density of MCC increased by 31% when nitrate was added into the catholyte.

  11. Reticular Synthesis of a Series of HKUST-like MOFs with Carbon Dioxide Capture and Separation.

    PubMed

    He, Hongming; Sun, Fuxing; Ma, Shengqian; Zhu, Guangshan

    2016-09-01

    We reported a series of HKUST-like MOFs based on multiple copper-containing secondary building units (SBUs). Compound 1 is constructed by two SBUs: Cu2(CO2)4 paddle-wheel SBUs and Cu2I2 dimer SBUs. Compound 2 has Cu2(CO2)4 paddle-wheel SBUs and Cu4I4 SBUs. Furthermore, compound 3 possesses Cu2(CO2)4 paddle-wheel SBUs, Cu2I2 dimer SBUs, and Cu(CO2)4 SBUs. These compounds are promising materials for CO2 capture and separation, because they all display commendable adsorption of CO2 and high selectivity for CO2 over CH4 and N2. It is worthy to note that compound 1 exhibits the highest Brunauer-Emmett-Teller surface area (ca. 901 m(2) g(-1)) among the MOF materials based on CuxIy SBUs. In addition, compound 3 is the first case that three copper SBUs coexist in MOFs. PMID:27556744

  12. Mixed-Metal Zeolitic Imidazolate Frameworks and their Selective Capture of Wet Carbon Dioxide over Methane.

    PubMed

    Nguyen, Nhung T T; Lo, Tien N H; Kim, Jaheon; Nguyen, Huong T D; Le, Toan B; Cordova, Kyle E; Furukawa, Hiroyasu

    2016-06-20

    A presynthesized, square planar copper imidazole complex, [Cu(imidazole)4](NO3)2, was utilized as a precursor in the synthesis of a new series of zeolitic imidazolate frameworks, termed ZIF-202, -203, and -204. The structures of all three members were solved by single-crystal X-ray diffraction analysis, which revealed ZIF-203 and -204 having successfully integrated square planar units within the backbones of their respective frameworks. As a result of this unit, the structures of both ZIF-203 and -204 were found to adopt unprecedented three-dimensional nets, namely, ntn and thl, respectively. One member of this series, ZIF-204, was demonstrated to be highly porous, exhibit exceptional stability in water, and selectively capture CO2 over CH4 under both dry and wet conditions without any loss in performance over three cycles. Remarkably, the regeneration of ZIF-204 was performed under the mild conditions of flowing a pure N2 gas through the material at ambient temperature. PMID:27248714

  13. THE UBIQUITY OF THE RAPID NEUTRON-CAPTURE PROCESS

    SciTech Connect

    Roederer, Ian U.; Sneden, Christopher; Cowan, John J.; Karakas, Amanda I.; Kratz, Karl-Ludwig; Lugaro, Maria; Simmerer, Jennifer; Farouqi, Khalil

    2010-12-01

    To better characterize the abundance patterns produced by the r-process, we have derived new abundances or upper limits for the heavy elements zinc (Zn, Z= 30), yttrium (Y, Z= 39), lanthanum (La, Z= 57), europium (Eu, Z= 63), and lead (Pb, Z= 82). Our sample of 161 metal-poor stars includes new measurements from 88 high-resolution and high signal-to-noise spectra obtained with the Tull Spectrograph on the 2.7 m Smith Telescope at the McDonald Observatory, and other abundances are adopted from the literature. We use models of the s-process in asymptotic giant branch stars to characterize the high Pb/Eu ratios produced in the s-process at low metallicity, and our new observations then allow us to identify a sample of stars with no detectable s-process material. In these stars, we find no significant increase in the Pb/Eu ratios with increasing metallicity. This suggests that s-process material was not widely dispersed until the overall Galactic metallicity grew considerably, perhaps even as high as [Fe/H] =-1.4, in contrast with earlier studies that suggested a much lower mean metallicity. We identify a dispersion of at least 0.5 dex in [La/Eu] in metal-poor stars with [Eu/Fe] <+0.6 attributable to the r-process, suggesting that there is no unique 'pure' r-process elemental ratio among pairs of rare earth elements. We confirm earlier detections of an anti-correlation between Y/Eu and Eu/Fe bookended by stars strongly enriched in the r-process (e.g., CS 22892-052) and those with deficiencies of the heavy elements (e.g., HD 122563). We can reproduce the range of Y/Eu ratios using simulations of high-entropy neutrino winds of core-collapse supernovae that include charged-particle and neutron-capture components of r-process nucleosynthesis. The heavy element abundance patterns in most metal-poor stars do not resemble that of CS 22892-052, but the presence of heavy elements such as Ba in nearly all metal-poor stars without s-process enrichment suggests that the r-process

  14. Moving from Misinformation Derived from Public Attitude Surveys on Carbon Dioxide Capture and Storage toward Realistic Stakeholder Involvement

    SciTech Connect

    Malone, Elizabeth L.; Dooley, James J.; Bradbury, Judith A.

    2010-03-01

    Stakeholder involvement can include many activities, from providing information on a website to one-on-one conversations with people confronting an issue in their community. For carbon dioxide capture and storage (CCS) a major tool of SI to date has been the survey. Recent surveys and other research into stakeholder involvement focused on the nascent commercial deployment of CCS technologies have provided valuable information about the state of general knowledge and attitudes toward these technologies. Most importantly, these research efforts reveal that the general public has relatively little knowledge about CCS. Given this lack of knowledge with respect to the concept of CCS let alone first-hand experiential knowledge derived from seeing these technologies deployed in local communities this paper critiques the methodology and results of the survey research. Then the framing of SI in CCS is examined, including the assumption that clear stakeholder acceptance is a realistic goal and that the public has a decisive say in choosing the energy technologies of the present and the future. Finally, a broader suite of SI activities is recommended as more suited to realistic and contextual goals.

  15. Patient flow scorecards capture complexity in the patient flow process.

    PubMed

    2014-07-01

    To get a larger, more holistic view of the patient flow process, a multidisciplinary improvement team at Children's Hospital of Philadelphia (CHOP) developed a five-domain patient flow scorecard. Each domain has several weighted sub-metrics that add up to 20 points, so the maximum number of points in the composite score is 100. Improvement team leaders say the approach has helped them home in on specific reasons for hold-ups so that resources can be focused in the most effective way. The "ED and ED-to-inpatient transition" domain includes eight sub-metrics that cover five specific time intervals, the leave-without-being-seen (LWBS) rate, and two adjustment measures that are used to account for high volumes and high admission rates from the ED. The other domains cover bed management, the discharge process, room turnover and environmental services, and scheduling and utilization. Administrators say it is important to establish metrics that can be captured easily along with entry points that tie in with workflows.

  16. Simulation of the capture process in the Fermilab Booster

    SciTech Connect

    Stahl, S.; Ankenbrandt, C.

    1987-09-01

    A progress report on efforts to understand and improve adiabatic capture in the Fermilab Booster by experiment and simulation is presented. In particular, a new RF voltage program for capture which ameliorates transverse space-charge effects is described and simulated. 7 refs., 4 figs.

  17. Process for removal of sulfur dioxide from gas streams

    SciTech Connect

    Pike, D.E.

    1982-02-02

    An improved apparatus and process are disclosed for the removal of sulfur oxides such as sulfur dioxide from waste gas streams. The process comprises scrubbing the waste gas with a circulating aqueous sodium sulfite/sodium bisulfite absorption solution at a relatively low ph followed by subjecting a portion of the circulating absorption solution to an improved multi-stage regeneration procedure wherein lime is employed to regenerate sulfite from bisulfite. The bleed from the scrubbing step which is subjected to regneration has a low ph and hence can dissolve more lime thereby increasing the lime utilization efficiency. In the regeneration procedure, a lime slurry is separated into a slurry of coarser lime particles and a second portion which contains very fine lime particles. The main regeneration is accomplished by adding the coarse lime slurry to the scrubber bleed. Due to the low ph in this reaction, not all the bisulfite is regenerated to sulfite. However, any remaining bisulfite is regenerated to sulfite in later regeneration steps by reaction with the second portion of the lime slurry in order to precipitate as much calcium as possible in the form of sulfate.

  18. Cyclic process for the removal of sulfur dioxide and the recovery of sulfur from gases

    SciTech Connect

    Lo, C.L.

    1991-11-19

    This patent describes a process for the removal of sulfur dioxide from a gas containing sulfur dioxide. It comprises contacting a gas containing sulfur dioxide with an aqueous solution comprising water, ferric chloride and a salt selected from the group consisting of barium chloride and calcium chloride to form ferrous chloride, hydrochloric acid and a precipitate selected from the group consisting of barium sulfate and calcium sulfate; and treating the aqueous solution with an oxidizing agent to convert ferrous chloride to ferric chloride.

  19. IMPACCT: Carbon Capture Technology

    SciTech Connect

    2012-01-01

    IMPACCT Project: IMPACCT’s 15 projects seek to develop technologies for existing coal-fired power plants that will lower the cost of carbon capture. Short for “Innovative Materials and Processes for Advanced Carbon Capture Technologies,” the IMPACCT Project is geared toward minimizing the cost of removing carbon dioxide (CO2) from coal-fired power plant exhaust by developing materials and processes that have never before been considered for this application. Retrofitting coal-fired power plants to capture the CO2 they produce would enable greenhouse gas reductions without forcing these plants to close, shifting away from the inexpensive and abundant U.S. coal supply.

  20. Large Scale U.S. Unconventional Fuels Production and the Role of Carbon Dioxide Capture and Storage Technologies in Reducing Their Greenhouse Gas Emissions

    SciTech Connect

    Dooley, James J.; Dahowski, Robert T.

    2008-11-18

    This paper examines the role that carbon dioxide capture and storage technologies could play in reducing greenhouse gas emissions if a significant unconventional fuels industry were to develop within the United States. Specifically, the paper examines the potential emergence of a large scale domestic unconventional fuels industry based on oil shale and coal-to-liquids (CTL) technologies. For both of these domestic heavy hydrocarbon resources, this paper models the growth of domestic production to a capacity of 3 MMB/d by 2050. For the oil shale production case, we model large scale deployment of an in-situ retorting process applied to the Eocene Green River formation of Colorado, Utah, and Wyoming where approximately 75% of the high grade oil shale resources within the United States lies. For the CTL case, we examine a more geographically dispersed coal-based unconventional fuel industry. This paper examines the performance of these industries under two hypothetical climate policies and concludes that even with the wide scale availability of cost effective carbon dioxide capture and storage technologies, these unconventional fuels production industries would be responsible for significant increases in CO2 emissions to the atmosphere. The oil shale production facilities required to produce 3MMB/d would result in net emissions to the atmosphere of between 3000-7000 MtCO2 in addition to storing potentially 1000 to 5000 MtCO2 in regional deep geologic formations in the period up to 2050. A similarly sized domestic CTL industry could result in 4000 to 5000 MtCO2 emitted to the atmosphere in addition to potentially 21,000 to 22,000 MtCO2 stored in regional deep geologic formations over the same period up to 2050. Preliminary analysis of regional CO2 storage capacity in locations where such facilities might be sited indicates that there appears to be sufficient storage capacity, primarily in deep saline formations, to accommodate the CO2 from these industries. However

  1. Analysis of electron capture process in charge pumping sequence using time domain measurements

    NASA Astrophysics Data System (ADS)

    Hori, Masahiro; Watanabe, Tokinobu; Tsuchiya, Toshiaki; Ono, Yukinori

    2014-12-01

    A method for analyzing the electron capture process in the charge pumping (CP) sequence is proposed and demonstrated. The method monitors the electron current in the CP sequence in time domain. This time-domain measurements enable us to directly access the process of the electron capture to the interface defects, which are obscured in the conventional CP method. Using the time-domain measurements, the rise time dependence of the capture process is systematically investigated. We formulate the capture process based on the rate equation and derive an analytic form of the current due to the electron capture to the defects. Based on the formula, the experimental data are analyzed and the capture cross section is obtained. In addition, the time-domain data unveil that the electron capture process completes before the electron channel opens, or below the threshold voltage in a low frequency range of the pulse.

  2. Analysis of electron capture process in charge pumping sequence using time domain measurements

    SciTech Connect

    Hori, Masahiro Watanabe, Tokinobu; Ono, Yukinori; Tsuchiya, Toshiaki

    2014-12-29

    A method for analyzing the electron capture process in the charge pumping (CP) sequence is proposed and demonstrated. The method monitors the electron current in the CP sequence in time domain. This time-domain measurements enable us to directly access the process of the electron capture to the interface defects, which are obscured in the conventional CP method. Using the time-domain measurements, the rise time dependence of the capture process is systematically investigated. We formulate the capture process based on the rate equation and derive an analytic form of the current due to the electron capture to the defects. Based on the formula, the experimental data are analyzed and the capture cross section is obtained. In addition, the time-domain data unveil that the electron capture process completes before the electron channel opens, or below the threshold voltage in a low frequency range of the pulse.

  3. Carbon Dioxide Reduction Post-Processing Sub-System Development

    NASA Technical Reports Server (NTRS)

    Abney, Morgan B.; Miller, Lee A.; Greenwood, Zachary; Barton, Katherine

    2012-01-01

    The state-of-the-art Carbon Dioxide (CO2) Reduction Assembly (CRA) on the International Space Station (ISS) facilitates the recovery of oxygen from metabolic CO2. The CRA utilizes the Sabatier process to produce water with methane as a byproduct. The methane is currently vented overboard as a waste product. Because the CRA relies on hydrogen for oxygen recovery, the loss of methane ultimately results in a loss of oxygen. For missions beyond low earth orbit, it will prove essential to maximize oxygen recovery. For this purpose, NASA is exploring an integrated post-processor system to recover hydrogen from CRA methane. The post-processor, called a Plasma Pyrolysis Assembly (PPA) partially pyrolyzes methane to recover hydrogen with acetylene as a byproduct. In-flight operation of post-processor will require a Methane Purification Assembly (MePA) and an Acetylene Separation Assembly (ASepA). Recent efforts have focused on the design, fabrication, and testing of these components. The results and conclusions of these efforts will be discussed as well as future plans.

  4. CO2 Capture with Liquid-to-Solid Absorbents: CO2 Capture Process Using Phase-Changing Absorbents

    SciTech Connect

    2010-10-01

    IMPACCT Project: GE and the University of Pittsburgh are developing a unique CO2 capture process in which a liquid absorbent, upon contact with CO2, changes into a solid phase. Once in solid form, the material can be separated and the CO2 can be released for storage by heating. Upon heating, the absorbent returns to its liquid form, where it can be reused to capture more CO2. The approach is more efficient than other solventbased processes because it avoids the heating of extraneous solvents such as water. This ultimately leads to a lower cost of CO2 capture and will lower the additional cost to produce electricity for coal-fired power plants that retrofit their facilities to include this technology.

  5. Electron-exchange effects on the charge capture process in degenerate quantum plasmas

    SciTech Connect

    Jung, Young-Dae; Akbari-Moghanjoughi, M.

    2014-03-15

    The electron-exchange effects on the charge capture process are investigated in degenerate quantum plasmas. The Bohr-Lindhard formalism with the effective interaction potential is employed to obtain the charge capture radius, capture probability, and capture cross section as functions of the impact parameter, projectile energy, electron-exchange parameter, Fermi energy, and plasmon energy. The result shows that the electron-exchange effect enhances the charge capture radius and the charge capture cross section in semiconductor quantum plasmas. It is also found that the charge capture radius and charge capture cross section increases with an increase of the Fermi energy and, however, decreases with increasing plasmon energy. Additionally, it is found that the peak position of the charge capture cross section is receded from the collision center with an increase of the electron-exchange parameter.

  6. Thermodynamic and Experimental Study of the Energetic Cost Involved in the Capture of Carbon Dioxide by Aqueous Mixtures of Commonly Used Primary and Tertiary Amines.

    PubMed

    Arcis, Hugues; Coulier, Yohann; Coxam, Jean-Yves

    2016-01-01

    The capture of carbon dioxide with chemical solvents is one solution to mitigate greenhouse gas emissions from anthropogenic sources and thus tackle climate change. Recent research has been focused on optimizing new kinds of advanced absorbents including aqueous amine blends, but critical downsides such as the large energetic cost involved with the industrial process remain. To address this issue, a better understanding of the energetic interactions existing in solution is necessary. In this paper, we report direct experimental measurements of the energy cost involved in the solvation of CO2 in two aqueous amine blends at different temperatures. The chemical solvents were designed as aqueous mixtures of commonly used primary and tertiary amines to study the influence of the different chemical properties inferred by the amine class. We have also applied a thermodynamic model to represent the energetic effects that take place in solution during CO2 dissolution in these mixtures, where all parameters were taken from previous studies focused on single amine absorbents. The noteworthy agreement observed with the reported experimental heats of absorption and with literature vapor liquid equilibrium properties confirmed the relevance of the underlying molecular mechanisms considered in our model, and suggest that this model would prove useful to investigate CO2 dissolution in other amine blends.

  7. Quantum chemical studies on solvents for post-combustion carbon dioxide capture: calculation of pKa and carbamate stability of disubstituted piperazines.

    PubMed

    Gangarapu, Satesh; Wierda, Gerben J; Marcelis, Antonius T M; Zuilhof, Han

    2014-06-23

    Piperazine is a widely studied solvent for post-combustion carbon dioxide capture. To investigate the possibilities of further improving this process, the electronic and steric effects of -CH(3), -CH(2)F, -CH(2)OH, -CH(2)NH(2), -COCH3 , and -CN groups of 2,5-disubstituted piperazines on the pKa and carbamate stability towards hydrolysis are investigated by quantum chemical methods. For the calculations, B3LYP, M11L, and spin-component-scaled MP2 (SCS-MP2) methods are used and coupled with the SMD solvation model. The experimental pK(a) values of piperazine, 2-methylpiperazine, and 2,5-dimethylpiperazine agree well with the calculated values. The present study indicates that substitution of -CH(3), -CH(2) NH(2), and -CH(2) OH groups on the 2- and 5-positions of piperazine has a positive impact on the CO(2) absorption capacity by reducing the carbamate stability towards hydrolysis. Furthermore, their higher boiling points, relative to piperazine itself, will lead to a reduction of volatility-related losses. PMID:24782140

  8. New Technical Risk Management Development for Carbon Capture Process

    SciTech Connect

    Engel, David W.; Letellier, Bruce; Edwards, Brian; Leclaire, Rene; Jones, Edward

    2012-04-30

    The basic CCSI objective of accelerating technology development and commercial deployment of carbon capture technologies through the extensive use of numerical simulation introduces a degree of unfamiliarity and novelty that potentially increases both of the traditional risk elements. In order to secure investor confidence and successfully accelerate the marketability of carbon capture technologies, it is critical that risk management decision tools be developed in parallel with numerical simulation capabilities and uncertainty quantification efforts. The focus of this paper is on the development of a technical risk model that incorporates the specific technology maturity development (level).

  9. Twin-column CaptureSMB: a novel cyclic process for protein A affinity chromatography.

    PubMed

    Angarita, Monica; Müller-Späth, Thomas; Baur, Daniel; Lievrouw, Roel; Lissens, Geert; Morbidelli, Massimo

    2015-04-10

    A twin-column counter-current chromatography processes, CaptureSMB, was used for the protein A affinity capture of a monoclonal antibody (mAb). By means of sequential loading, the process improves the utilization of the stationary phase by achieving loadings much closer to the static binding capacity of the resin in comparison to batch chromatography. Using a mAb capture case study with protein A affinity chromatography, the performance and product quality obtained from CaptureSMB and batch processes were compared. The effect of the flow rate, column length and titer concentration on the process performance and product quality were evaluated. CaptureSMB showed superior performance compared to batch chromatography with respect to productivity, capacity utilization, product concentration and buffer consumption. A simplified economic evaluation showed that CaptureSMB could decrease resin costs of 10-30% depending on the manufacturing scenario.

  10. Twin-column CaptureSMB: a novel cyclic process for protein A affinity chromatography.

    PubMed

    Angarita, Monica; Müller-Späth, Thomas; Baur, Daniel; Lievrouw, Roel; Lissens, Geert; Morbidelli, Massimo

    2015-04-10

    A twin-column counter-current chromatography processes, CaptureSMB, was used for the protein A affinity capture of a monoclonal antibody (mAb). By means of sequential loading, the process improves the utilization of the stationary phase by achieving loadings much closer to the static binding capacity of the resin in comparison to batch chromatography. Using a mAb capture case study with protein A affinity chromatography, the performance and product quality obtained from CaptureSMB and batch processes were compared. The effect of the flow rate, column length and titer concentration on the process performance and product quality were evaluated. CaptureSMB showed superior performance compared to batch chromatography with respect to productivity, capacity utilization, product concentration and buffer consumption. A simplified economic evaluation showed that CaptureSMB could decrease resin costs of 10-30% depending on the manufacturing scenario. PMID:25748537

  11. Acceleration of integral imaging based incoherent Fourier hologram capture using graphic processing unit.

    PubMed

    Jeong, Kyeong-Min; Kim, Hee-Seung; Hong, Sung-In; Lee, Sung-Keun; Jo, Na-Young; Kim, Yong-Soo; Lim, Hong-Gi; Park, Jae-Hyeung

    2012-10-01

    Speed enhancement of integral imaging based incoherent Fourier hologram capture using a graphic processing unit is reported. Integral imaging based method enables exact hologram capture of real-existing three-dimensional objects under regular incoherent illumination. In our implementation, we apply parallel computation scheme using the graphic processing unit, accelerating the processing speed. Using enhanced speed of hologram capture, we also implement a pseudo real-time hologram capture and optical reconstruction system. The overall operation speed is measured to be 1 frame per second.

  12. Low-Energy Solvents For Carbon Dioxide Capture Enabled By A Combination Of Enzymes And Vacuum Regeneration

    SciTech Connect

    Salmon, Sonja; House, Alan; Liu, Kun; Frimpong, Reynolds; Liu, Kunlei; Freeman, Charles; Whyatt, Greg; Slater, Jonathan; Fitzgerald, David

    2015-08-31

    An integrated bench-scale system combining the attributes of the bio-renewable enzyme carbonic anhydrase (CA) with low-enthalpy CO2 absorption solvents and vacuum regeneration was designed, built and operated for 500 hours using simulated flue gas. The objective was to develop a CO2 capture process with improved efficiency and sustainability when compared to NETL Case 10 monoethanolamine (MEA) scrubbing technology. The use of CA accelerates inter-conversion between dissolved CO2 and bicarbonate ion to enhance CO2 absorption, and the use of low enthalpy CO2 absorption solvents makes it possible to regenerate the solvent at lower temperatures relative to the reference MEA-based solvent. The vacuum regeneration-based integrated bench-scale system operated successfully for an accumulated 500 hours using aqueous 23.5 wt% K2CO3-based solvent containing 2.5 g/L enzyme to deliver an average 84% CO2 capture when operated with a 20% enzyme replenishment rate per ~7 hour steady-state run period. The total inlet gas flow was 30 standard liters per minute with 15% CO2 and 85% N2. The absorber temperature was 40°C and the stripper operated under 35 kPa pressure with an approximate 77°C stripper bottom temperature. Tests with a 30°C absorber temperature delivered >90% capture. On- and off-line operational measurements provided a full process data set, with recirculating enzyme, that allowed for enzyme replenishment and absorption/desorption kinetic parameter calculations. Dissolved enzyme replenishment and conventional process controls were demonstrated as straightforward approaches to maintain system performance. Preliminary evaluation of a novel flow-through ultrasonically enhanced regeneration system was also conducted, yet resulted in CO2 release within the range of temperature-dependent release, and further work would be needed to validate the benefits of ultrasonic enhanced stripping. A full technology assessment was completed in which four techno-economic cases for

  13. In situ Formation of a Monodispersed Spherical Mesoporous Nanosilica-Torlon Hollow-Fiber Composite for Carbon Dioxide Capture.

    PubMed

    Rownaghi, Ali A; Rezaei, Fateme; Labreche, Ying; Brennan, Patrick J; Johnson, Justin R; Li, Fuyue Stephanie; Koros, William J

    2015-10-26

    We describe a new template-free method for the in situ formation of a monodispersed spherical mesoporous nanosilica-Torlon hollow-fiber composite. A thin layer of Torlon hollow fiber that comprises silica nanoparticles was created by the in situ extrusion of a tetraethyl orthosilicate/N-methyl-2-pyrrolidone solution in a sheath layer and a Torlon polymer dope in a core support layer. This new method can be integrated easily into current hollow-fiber composite fabrication processes. The hollow-fiber composites were then functionalized with 3-aminopropyltrimethoxy silane (APS) and evaluated for their CO2 -capture performance. The resulting APS-functionalized mesoporous silica nanoparticles/Torlon hollow fibers exhibited a high CO2 equilibrium capacity of 1.5 and 1.9 mmol g(-1) at 35 and 60 °C, respectively, which is significantly higher than values for fiber sorbents without nanoparticles reported previously. PMID:26355795

  14. Membrane loop process for separating carbon dioxide for use in gaseous form from flue gas

    SciTech Connect

    Wijmans, Johannes G; Baker, Richard W; Merkel, Timothy C

    2014-10-07

    The invention is a process involving membrane-based gas separation for separating and recovering carbon dioxide emissions from combustion processes in partially concentrated form, and then transporting the carbon dioxide and using or storing it in a confined manner without concentrating it to high purity. The process of the invention involves building up the concentration of carbon dioxide in a gas flow loop between the combustion step and a membrane separation step. A portion of the carbon dioxide-enriched gas can then be withdrawn from this loop and transported, without the need to liquefy the gas or otherwise create a high-purity stream, to a destination where it is used or confined, preferably in an environmentally benign manner.

  15. Neutron Capture Reactions on Fe and Ni Isotopes for the Astrophysical s-process

    SciTech Connect

    Lederer, C.; Giubrone, G.; Massimi, C.; Žugec, P.; Barbagallo, M.; Colonna, N.; Domingo-Pardo, C.; Guerrero, C.; Gunsing, F.; Käppeler, F.; Tain, J.L.; Altstadt, S.; Andrzejewski, J.; Audouin, L.; Bečvář, F.; and others

    2014-06-15

    Neutron capture cross sections in the keV neutron energy region are the key nuclear physics input to study the astrophysical slow neutron capture process. In the past years, a series of neutron capture cross section measurements has been performed at the neutron time-of-flight facility n{sub T}OF at CERN focussing on the Fe/Ni mass region. Recent results and future developments in the neutron time-of-flight technique are discussed.

  16. Silica-coated multi-walled carbon nanotubes impregnated with polyethyleneimine for carbon dioxide capture under the flue gas condition

    SciTech Connect

    Lee, Min-Sang; Park, Soo-Jin

    2015-03-15

    In this study, silica-coated multi-walled carbon nanotubes impregnated with polyethyleneimine (PEI) were prepared via a two-step process: (i) hydrolysis of tetraethylorthosilicate onto multi-walled carbon nanotubes, and (ii) impregnation of PEI. The adsorption properties of CO{sub 2} were investigated using CO{sub 2} adsorption–desorption isotherms at 298 K and thermogravimetric analysis under the flue gas condition (15% CO{sub 2}/85% N{sub 2}). The results obtained in this study indicate that CO{sub 2} adsorption increases after impregnation of PEI. The increase in CO{sub 2} capture was attributed to the affinity between CO{sub 2} and the amine groups. CO{sub 2} adsorption–desorption experiments, which were repeated five times, also showed that the prepared adsorbents have excellent regeneration properties. - Graphical abstract: Fabrication and CO{sub 2} adsorption process of the S-MWCNTs impregnated with PEI. - Highlights: • Silica coated-MWCNT impregnated with PEI was synthesized. • Amine groups of PEI gave CO{sub 2} affinity sites on MWCNT surfaces. • The S-MWCNT/PEI(50) exhibited the highest CO{sub 2} adsorption capacity.

  17. Comparison of batch and continuous multi-column protein A capture processes by optimal design.

    PubMed

    Baur, Daniel; Angarita, Monica; Müller-Späth, Thomas; Steinebach, Fabian; Morbidelli, Massimo

    2016-07-01

    Multi-column capture processes show several advantages compared to batch capture. It is however not evident how many columns one should use exactly. To investigate this issue, twin-column CaptureSMB, 3- and 4-column periodic counter-current chromatography (PCC) and single column batch capture are numerically optimized and compared in terms of process performance for capturing a monoclonal antibody using protein A chromatography. Optimization is carried out with respect to productivity and capacity utilization (amount of product loaded per cycle compared to the maximum amount possible), while keeping yield and purity constant. For a wide range of process parameters, all three multi-column processes show similar maximum capacity utilization and performed significantly better than batch. When maximizing productivity, the CaptureSMB process shows optimal performance, except at high feed titers, where batch chromatography can reach higher productivity values than the multi-column processes due to the complete decoupling of the loading and elution steps, albeit at a large cost in terms of capacity utilization. In terms of trade-off, i.e. how much the capacity utilization decreases with increasing productivity, CaptureSMB is optimal for low and high feed titers, whereas the 3-column process is optimal in an intermediate region. Using these findings, the most suitable process can be chosen for different production scenarios.

  18. Comparison of batch and continuous multi-column protein A capture processes by optimal design.

    PubMed

    Baur, Daniel; Angarita, Monica; Müller-Späth, Thomas; Steinebach, Fabian; Morbidelli, Massimo

    2016-07-01

    Multi-column capture processes show several advantages compared to batch capture. It is however not evident how many columns one should use exactly. To investigate this issue, twin-column CaptureSMB, 3- and 4-column periodic counter-current chromatography (PCC) and single column batch capture are numerically optimized and compared in terms of process performance for capturing a monoclonal antibody using protein A chromatography. Optimization is carried out with respect to productivity and capacity utilization (amount of product loaded per cycle compared to the maximum amount possible), while keeping yield and purity constant. For a wide range of process parameters, all three multi-column processes show similar maximum capacity utilization and performed significantly better than batch. When maximizing productivity, the CaptureSMB process shows optimal performance, except at high feed titers, where batch chromatography can reach higher productivity values than the multi-column processes due to the complete decoupling of the loading and elution steps, albeit at a large cost in terms of capacity utilization. In terms of trade-off, i.e. how much the capacity utilization decreases with increasing productivity, CaptureSMB is optimal for low and high feed titers, whereas the 3-column process is optimal in an intermediate region. Using these findings, the most suitable process can be chosen for different production scenarios. PMID:26992151

  19. Whiteboard sharing: capture, process, and print or email

    NASA Astrophysics Data System (ADS)

    Gormish, Michael; Erol, Berna; Van Olst, Daniel G.; Li, Tim; Mariotti, Andrea

    2011-03-01

    Whiteboards support face to face meetings by facilitating the sharing of ideas, focusing attention, and summarizing. However, at the end of the meeting participants desire some record of the information from the whiteboard. While there are whiteboards with built-in printers, they are expensive and relatively uncommon. We consider the capture of the information on a whiteboard with a mobile phone, improving the image quality with a cloud service, and sharing the results. This paper describes the algorithm for improving whiteboard image quality, the user experience for both a web widget and a smartphone application, and the necessary adaptations for providing this as a web service. The web widget, and mobile apps for both iPhone and Android are currently freely available, and have been used by more than 50,000 people.

  20. Bisphosphine dioxides

    DOEpatents

    Moloy, Kenneth G.

    1990-01-01

    A process for the production of organic bisphosphine dioxides from organic bisphosphonates. The organic bisphosphonate is reacted with a Grignard reagent to give relatively high yields of the organic bisphosphine dioxide.

  1. Bisphosphine dioxides

    SciTech Connect

    Moloy, K.G.

    1990-02-20

    A process is described for the production of organic bisphosphine dioxides from organic bisphosphonates. The organic bisphosphonate is reacted with a Grignard reagent to give relatively high yields of the organic bisphosphine dioxide.

  2. Computational Tools for Accelerating Carbon Capture Process Development

    SciTech Connect

    Miller, David; Sahinidis, N V; Cozad, A; Lee, A; Kim, H; Morinelly, J; Eslick, J; Yuan, Z

    2013-06-04

    This presentation reports development of advanced computational tools to accelerate next generation technology development. These tools are to develop an optimized process using rigorous models. They include: Process Models; Simulation-Based Optimization; Optimized Process; Uncertainty Quantification; Algebraic Surrogate Models; and Superstructure Optimization (Determine Configuration).

  3. SEMICONDUCTOR TECHNOLOGY Supercritical carbon dioxide process for releasing stuck cantilever beams

    NASA Astrophysics Data System (ADS)

    Yu, Hui; Chaoqun, Gao; Lei, Wang; Yupeng, Jing

    2010-10-01

    The multi-SCCO2 (supercritical carbon dioxide) release and dry process based on our specialized SCCO2 semiconductor process equipment is investigated and the releasing mechanism is discussed. The experiment results show that stuck cantilever beams were held up again under SCCO2 high pressure treatment and the repeatability of this process is nearly 100%.

  4. A research needs assessment for the capture, utilization and disposal of carbon dioxide from fossil fuel-fired power plants. Volume 1, Executive summary: Final report

    SciTech Connect

    Not Available

    1993-07-01

    This study identifies and assesses system approaches in order to prioritize research needs for the capture and non-atmospheric sequestering of a significant portion of the carbon dioxide (CO{sub 2}) emitted from fossil fuel-fired electric power plants (US power plants presently produce about 7% of the world`s CO{sub 2} emissions). The study considers capture technologies applicable either to existing plants or to those that optimistically might be demonstrated on a commercial scale over the next twenty years. Specific conclusions are as follows: (1) To implement CO{sub 2} capture and sequestration on a national scale will decrease power plant net efficiencies and significantly increase the cost of electricity. To make responsible societal decisions, accurate and consistent economic and environmental analysis of all alternatives for atmospheric CO{sub 2} mitigation are required. (2) Commercial CO{sub 2} capture technology, though expensive and energy intensive, exists today. (3) The most promising approach to more economical CO{sub 2} capture is to develop power plant systems that facilitate efficient CO{sub 2} capture. (4) While CO{sub 2} disposal in depleted oil and gas reservoirs is feasible today, the ability to dispose of large quantities Of CO{sub 2} is highly uncertain because of both technical and institutional issues. Disposal into the deep ocean or confined aquifers offers the potential for large quantity disposal, but there are technical, safety, liability, and environmental issues to resolve. Therefore, the highest priority research should focus on establishing the feasibility of large scale disposal options.

  5. A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries

    PubMed Central

    2011-01-01

    Genome targeting methods enable cost-effective capture of specific subsets of the genome for sequencing. We present here an automated, highly scalable method for carrying out the Solution Hybrid Selection capture approach that provides a dramatic increase in scale and throughput of sequence-ready libraries produced. Significant process improvements and a series of in-process quality control checkpoints are also added. These process improvements can also be used in a manual version of the protocol. PMID:21205303

  6. Synthesis of High-Surface-Area Nitrogen-Doped Porous Carbon Microflowers and Their Efficient Carbon Dioxide Capture Performance.

    PubMed

    Li, Yao; Cao, Minhua

    2015-07-01

    Sustainable carbon materials have received particular attention in CO2 capture and storage owing to their abundant pore structures and controllable pore parameters. Here, we report high-surface-area hierarchically porous N-doped carbon microflowers, which were assembled from porous nanosheets by a three-step route: soft-template-assisted self-assembly, thermal decomposition, and KOH activation. The hydrazine hydrate used in our experiment serves as not only a nitrogen source, but also a structure-directing agent. The activation process was carried out under low (KOH/carbon=2), mild (KOH/carbon=4) and severe (KOH/carbon=6) activation conditions. The mild activated N-doped carbon microflowers (A-NCF-4) have a hierarchically porous structure, high specific surface area (2309 m(2)  g(-1)), desirable micropore size below 1 nm, and importantly large micropore volume (0.95 cm(3)  g(-1)). The remarkably high CO2 adsorption capacities of 6.52 and 19.32 mmol g(-1) were achieved with this sample at 0 °C (273 K) and two pressures, 1 bar and 20 bar, respectively. Furthermore, this sample also exhibits excellent stability during cyclic operations and good separation selectivity for CO2 over N2.

  7. High Purity Hydrogen Production with In-Situ Carbon Dioxide and Sulfur Capture in a Single Stage Reactor

    SciTech Connect

    Nihar Phalak; Shwetha Ramkumar; Daniel Connell; Zhenchao Sun; Fu-Chen Yu; Niranjani Deshpande; Robert Statnick; Liang-Shih Fan

    2011-07-31

    Enhancement in the production of high purity hydrogen (H{sub 2}) from fuel gas, obtained from coal gasification, is limited by thermodynamics of the water gas shift (WGS) reaction. However, this constraint can be overcome by conducting the WGS in the presence of a CO{sub 2}-acceptor. The continuous removal of CO{sub 2} from the reaction mixture helps to drive the equilibrium-limited WGS reaction forward. Since calcium oxide (CaO) exhibits high CO{sub 2} capture capacity as compared to other sorbents, it is an ideal candidate for such a technique. The Calcium Looping Process (CLP) developed at The Ohio State University (OSU) utilizes the above concept to enable high purity H{sub 2} production from synthesis gas (syngas) derived from coal gasification. The CLP integrates the WGS reaction with insitu CO{sub 2}, sulfur and halide removal at high temperatures while eliminating the need for a WGS catalyst, thus reducing the overall footprint of the hydrogen production process. The CLP comprises three reactors - the carbonator, where the thermodynamic constraint of the WGS reaction is overcome by the constant removal of CO{sub 2} product and high purity H{sub 2} is produced with contaminant removal; the calciner, where the calcium sorbent is regenerated and a sequestration-ready CO{sub 2} stream is produced; and the hydrator, where the calcined sorbent is reactivated to improve its recyclability. As a part of this project, the CLP was extensively investigated by performing experiments at lab-, bench- and subpilot-scale setups. A comprehensive techno-economic analysis was also conducted to determine the feasibility of the CLP at commercial scale. This report provides a detailed account of all the results obtained during the project period.

  8. Process for the enhanced capture of heavy metal emissions

    DOEpatents

    Biswas, Pratim; Wu, Chang-Yu

    2001-01-01

    This invention is directed to a process for forming a sorbent-metal complex. The process includes oxidizing a sorbent precursor and contacting the sorbent precursor with a metallic species. The process further includes chemically reacting the sorbent precursor and the metallic species, thereby forming a sorbent-metal complex. In one particular aspect of the invention, at least a portion of the sorbent precursor is transformed into sorbent particles during the oxidation step. These sorbent particles then are contacted with the metallic species and chemically reacted with the metallic species, thereby forming a sorbent-metal complex. Another aspect of the invention is directed to a process for forming a sorbent metal complex in a combustion system. The process includes introducing a sorbent precursor into a combustion system and subjecting the sorbent precursor to an elevated temperature sufficient to oxidize the sorbent precursor and transform the sorbent precursor into sorbent particles. The process further includes contacting the sorbent particles with a metallic species and exposing the sorbent particles and the metallic species to a complex-forming temperature whereby the metallic species reacts with the sorbent particles thereby forming a sorbent-metal complex under UV irradiation.

  9. Fabrication of zeolite/polymer multilayer composite membranes for carbon dioxide capture: Deposition of zeolite particles on polymer supports.

    PubMed

    Ramasubramanian, Kartik; Severance, Michael A; Dutta, Prabir K; Ho, W S Winston

    2015-08-15

    Membranes, due to their smaller footprint and potentially lower energy consumption than the amine process, offer a promising route for post-combustion CO2 capture. Zeolite Y based inorganic selective layers offer a favorable combination of CO2 permeance and CO2/N2 selectivity, membrane properties crucial to the economics. For economic viability on large scale, we propose to use flexible and scalable polymer supports for inorganic selective layers. The work described in this paper developed a detailed protocol for depositing thin zeolite Y seed layers on polymer supports, the first step in the synthesis of a polycrystalline zeolite Y membrane. We also studied the effects of support surface morphology (pore size and surface porosity) on the quality of deposition and identified favorable supports for the deposition. Two different zeolite Y particles with nominal sizes of 200 nm and 40 nm were investigated. To obtain a complete coverage of zeolite particles on the support surface with minimum defects and in a reproducible manner, a vacuum-assisted dip-coating technique was developed. Images obtained using both digital camera and optical microscope showed the presence of color patterns on the deposited surface which suggested that the coverage was complete. Electron microscopy revealed that the particle packing was dense with some drying cracks. Layer thickness with the larger zeolite Y particles was close to 1 μm while that with the smaller particles was reduced to less than 0.5 μm. In order to reduce drying cracks for layers with smaller zeolite Y particles, thickness was reduced by lowering the dispersion concentration. Transport measurement was used as an additional technique to characterize these layers.

  10. Capturing Problem-Solving Processes Using Critical Rationalism

    ERIC Educational Resources Information Center

    Chitpin, Stephanie; Simon, Marielle

    2012-01-01

    The examination of problem-solving processes continues to be a current research topic in education. Knowing how to solve problems is not only a key aspect of learning mathematics but is also at the heart of cognitive theories, linguistics, artificial intelligence, and computers sciences. Problem solving is a multistep, higher-order cognitive task…

  11. Standard services for the capture, processing, and distribution of packetized telemetry data

    NASA Technical Reports Server (NTRS)

    Stallings, William H.

    1989-01-01

    Standard functional services for the capture, processing, and distribution of packetized data are discussed with particular reference to the future implementation of packet processing systems, such as those for the Space Station Freedom. The major functions are listed under the following major categories: input processing, packet processing, and output processing. A functional block diagram of a packet data processing facility is presented, showing the distribution of the various processing functions as well as the primary data flow through the facility.

  12. Capturing User Needs to Improve Processes at EOSDIS Data Centers

    NASA Astrophysics Data System (ADS)

    Sofinowski, E. J.; Boquist, C. L.

    2009-12-01

    Since 2004 the Earth Observing System Data and Information System (EOSDIS) has conducted an annual comprehensive survey of user satisfaction using the American Customer Satisfaction Index (ACSI). Customer satisfaction ratings for EOSDIS consistently rate better than the overall government ratings. As part of the survey users are asked to submit comments concerning their experiences and interests. These user comments provide valuable insight into the effect of data center processes on users' experiences. Although user satisfaction has remained high, their preferences have changed with the rapid advances in web-based services. This analysis investigates the correlation between user comments, process changes or capability improvements at the individual data centers, and whether the changes at the data centers and web sites show a corresponding increase in user satisfaction. We will evaluate the comments in the areas of Product Search, Product Selection and Order, Delivery, Product Quality and Customer Support.

  13. A straightforward methodology for designing continuous monoclonal antibody capture multi-column chromatography processes.

    PubMed

    Gjoka, Xhorxhi; Rogler, Karl; Martino, Richard Alexander; Gantier, Rene; Schofield, Mark

    2015-10-16

    A simple process development strategy for continuous capture multi-column chromatography (MCC) is described. The approach involves a few single column breakthrough experiments, based on several simplifying observations that enable users to rapidly convert batch processes into well-designed multi-column processes. The method was validated using a BioSMB(®) (Pall Life Sciences) lab scale multi-column system and a mAb capture process employing Protein A resin. The approach enables users to optimize MCC processes based on their internal preferences and constraints without requiring any mathematical modeling expertise.

  14. Chromosome Conformation Capture on Chip (4C): Data Processing.

    PubMed

    Leblanc, Benjamin; Comet, Itys; Bantignies, Frédéric; Cavalli, Giacomo

    2016-01-01

    4C methods are useful to investigate dependencies between regulatory mechanisms and chromatin structures by revealing the frequency of chromatin contacts between a locus of interest and remote sequences on the chromosome. In this chapter we describe a protocol for the data analysis of microarray-based 4C experiments, presenting updated versions of the methods we used in a previous study of the large-scale chromatin interaction profile of a Polycomb response element in Drosophila. The protocol covers data preparation, normalization, microarray probe selection, and the multi-resolution detection of regions with enriched chromatin contacts. A reanalysis of two independent mouse datasets illustrates the versatility of this protocol and the importance of data processing in 4C. Methods were implemented in the R package MRA.TA (Multi-Resolution Analyses on Tiling Array data), and they can be used to analyze ChIP-on-chip data on broadly distributed chromatin components such as histone marks. PMID:27659990

  15. Radiative neutron captures by neutron-rich nuclei and the r-process nucleosynthesis

    NASA Astrophysics Data System (ADS)

    Goriely, S.

    1998-09-01

    The radiative neutron capture by neutron-rich nuclei is estimated with an improved description of the electric giant dipole resonance. In addition, 3 major effects affecting the capture rates by exotic neutron-rich nuclei are studied. These concern the existence of a low-energy E1 pygmy resonance, the overestimate of the statistical predictions for resonance-deficient nuclei and the direct capture mechanism. The total (n,γ) reaction rates including these 3 effects are evaluated for 3100 neutron-rich nuclei and used in parametric r-process calculations to analyze their impact on the r-abundance distribution.

  16. Capturing snapshots of APE1 processing DNA damage.

    PubMed

    Freudenthal, Bret D; Beard, William A; Cuneo, Matthew J; Dyrkheeva, Nadezhda S; Wilson, Samuel H

    2015-11-01

    DNA apurinic-apyrimidinic (AP) sites are prevalent noncoding threats to genomic stability and are processed by AP endonuclease 1 (APE1). APE1 incises the AP-site phosphodiester backbone, generating a DNA-repair intermediate that is potentially cytotoxic. The molecular events of the incision reaction remain elusive, owing in part to limited structural information. We report multiple high-resolution human APE1-DNA structures that divulge new features of the APE1 reaction, including the metal-binding site, the nucleophile and the arginine clamps that mediate product release. We also report APE1-DNA structures with a T-G mismatch 5' to the AP site, representing a clustered lesion occurring in methylated CpG dinucleotides. These structures reveal that APE1 molds the T-G mismatch into a unique Watson-Crick-like geometry that distorts the active site, thus reducing incision. These snapshots provide mechanistic clarity for APE1 while affording a rational framework to manipulate biological responses to DNA damage. PMID:26458045

  17. Capturing snapshots of APE1 processing DNA damage

    DOE PAGESBeta

    Freudenthal, Bret D.; Beard, William A.; Cuneo, Matthew J.; Dyrkheeva, Nadezhda S.; Wilson, Samuel H.

    2015-10-12

    DNA apurinic-apyrimidinic (AP) sites are prevalent noncoding threats to genomic stability and are processed by AP endonuclease 1 (APE1). APE1 incises the AP-site phosphodiester backbone, generating a DNA-repair intermediate that is potentially cytotoxic. The molecular events of the incision reaction remain elusive, owing in part to limited structural information. Here we report multiple high-resolution human APE1-DNA structures that divulge new features of the APE1 reaction, including the metal-binding site, the nucleophile and the arginine clamps that mediate product release. We also report APE1-DNA structures with a T-G mismatch 5' to the AP site, representing a clustered lesion occurring in methylatedmore » CpG dinucleotides. Moreover, these structures reveal that APE1 molds the T-G mismatch into a unique Watson-Crick-like geometry that distorts the active site, thus reducing incision. Finally, these snapshots provide mechanistic clarity for APE1 while affording a rational framework to manipulate biological responses to DNA damage.« less

  18. Capturing snapshots of APE1 processing DNA damage

    SciTech Connect

    Freudenthal, Bret D.; Beard, William A.; Cuneo, Matthew J.; Dyrkheeva, Nadezhda S.; Wilson, Samuel H.

    2015-10-12

    DNA apurinic-apyrimidinic (AP) sites are prevalent noncoding threats to genomic stability and are processed by AP endonuclease 1 (APE1). APE1 incises the AP-site phosphodiester backbone, generating a DNA-repair intermediate that is potentially cytotoxic. The molecular events of the incision reaction remain elusive, owing in part to limited structural information. Here we report multiple high-resolution human APE1-DNA structures that divulge new features of the APE1 reaction, including the metal-binding site, the nucleophile and the arginine clamps that mediate product release. We also report APE1-DNA structures with a T-G mismatch 5' to the AP site, representing a clustered lesion occurring in methylated CpG dinucleotides. Moreover, these structures reveal that APE1 molds the T-G mismatch into a unique Watson-Crick-like geometry that distorts the active site, thus reducing incision. Finally, these snapshots provide mechanistic clarity for APE1 while affording a rational framework to manipulate biological responses to DNA damage.

  19. Capturing Snapshots of APE1 Processing DNA Damage

    PubMed Central

    Freudenthal, Bret D.; Beard, William A.; Cuneo, Matthew J.; Dyrkheeva, Nadezhda S.; Wilson, Samuel H.

    2015-01-01

    DNA apurinic-apyrimidinic (AP) sites are prevalent non-coding threats to genomic stability and are processed by AP endonuclease 1 (APE1). APE1 incises the AP-site phosphodiester backbone, generating a DNA repair intermediate that is potentially cytotoxic. The molecular events of the incision reaction remain elusive due in part to limited structural information. We report multiple high-resolution human APE1:DNA structures that divulge novel features of the APE1 reaction, including the metal binding site, nucleophile, and arginine clamps that mediate product release. We also report APE1:DNA structures with a T:G mismatch 5′ to the AP-site, representing a clustered lesion occurring in methylated CpG dinucleotides. These reveal that APE1 molds the T:G mismatch into a unique Watson-Crick like geometry that distorts the active site reducing incision. These snapshots provide mechanistic clarity for APE1, while affording a rational framework to manipulate biological responses to DNA damage. PMID:26458045

  20. A research needs assessment for the capture, utilization and disposal of carbon dioxide from fossil fuel-fired power plants. Volume 2, Topical reports: Final report

    SciTech Connect

    Not Available

    1993-07-01

    This study, identifies and assesses system approaches in order to prioritize research needs for the capture and non-atmospheric sequestering of a significant portion of the carbon dioxide (CO{sub 2}) emitted from fossil fuel-fired electric power plants (US power plants presently produce about 7% of the world`s CO{sub 2} emissions). The study considers capture technologies applicable either to existing plants or to those that optimistically might be demonstrated on a commercial scale over the next twenty years. The research needs that have high priority in establishing the technical, environmental, and economic feasibility of large-scale capture and disposal of CO{sub 2} from electric power plants are:(1) survey and assess the capacity, cost, and location of potential depleted gas and oil wells that are suitable CO{sub 2} repositories (with the cooperation of the oil and gas industry); (2) conduct research on the feasibility of ocean disposal, with objectives of determining the cost, residence time, and environmental effects for different methods of CO{sub 2} injection; (3) perform an in-depth survey of knowledge concerning the feasibility of using deep, confined aquifers for disposal and, if feasible, identify potential disposal locations (with the cooperation of the oil and gas industry); (4) evaluate, on a common basis, system and design alternatives for integration of CO{sub 2} capture systems with emerging and advanced technologies for power generation; and prepare a conceptual design, an analysis of barrier issues, and a preliminary cost estimate for pipeline networks necessary to transport a significant portion of the CO{sub 2} to potentially feasible disposal locations.

  1. New phase equilibrium analyzer for determination of the vapor-liquid equilibrium of carbon dioxide and permanent gas mixtures for carbon capture and storage.

    PubMed

    Ke, Jie; Parrott, Andrew J; Sanchez-Vicente, Yolanda; Fields, Peter; Wilson, Richard; Drage, Trevor C; Poliakoff, Martyn; George, Michael W

    2014-08-01

    A high-pressure, phase equilibrium analyzer incorporating a fiber-optic reflectometer is described. The analyzer has been designed for measuring the vapor-liquid equilibrium data of multi-component mixtures of carbon dioxide and permanent gases, providing a novel tool to acquire of a large number of phase equilibrium data for the development of the new carbon capture and storage technologies. We demonstrate that the analyzer is suitable for determining both the bubble- and dew-point lines at temperature from 253 K and pressure up to 25 MPa using pure CO2 and two binary mixtures of CO2 + N2 and CO2 + H2. PMID:25173315

  2. DEMONSTRATION OF A LIQUID CARBON DIOXIDE PROCESS FOR CLEANING METAL PARTS

    EPA Science Inventory

    The report gives results of a demonstration of liquid carbon dioxide (LCO2) as an alternative to chlorinated solvents for cleaning metal parts. It describes the LCO2 process, the parts tested, the contaminants removed, and results from preliminary laboratory testing and on-site d...

  3. Fractionation of whey protein isolate with supercritical carbon dioxideprocess modeling and cost estimation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    An economical and environmentally friendly whey protein fractionation process was developed using supercritical carbon dioxide (sCO2) as an acid to produce enriched fractions of alpha-lactalbumin (alpha-La) and beta-lactoglobulin (beta-Lg) from a commercial whey protein isolate (WPI) containing 55% ...

  4. Fabrication and Scale-up of Polybenzimidazole (PBI) Membrane Based System for Precombustion-Based Capture of Carbon Dioxide

    SciTech Connect

    Krishnan, Gopala; Jayaweera, Indira; Sanjrujo, Angel; O'Brien, Kevin; Callahan, Richard; Berchtold, Kathryn; Roberts, Daryl-Lynn; Johnson, Will

    2012-03-31

    The primary objectives of this project are to (1) demonstrate the performance and fabrication of a technically and economically viable pre-combustion-based CO{sub 2} capture system based on the high temperature stability and permeance of PBI membranes, (2) optimize a plan for integration of PBI capture system into an IGCC plant and (3) develop a commercialization plan that addresses technical issues and business issues to outline a clear path for technology transfer of the PBI membrane technology. This report describes research conducted from April 1, 2007 to March 30, 2012 and focused on achieving the above objectives. PBI-based hollow fibers have been fabricated at kilometer lengths and bundled as modules at a bench-scale level for the separation of CO{sub 2} from H{sub 2} at high temperatures and pressures. Long term stability of these fibers has been demonstrated with a relatively high H{sub 2}/CO{sub 2} selectivity (35 to 50) and H{sub 2} permeance (80 GPU) at temperatures exceeding 225°C. Membrane performance simulations and systems analysis of an IGCC system incorporating a PBI hollow fiber membrane modules have demonstrated that the cost of electricity for CO{sub 2} capture (<10%) using such a high temperature separator. When the cost of transporting, storing, and monitoring the CO{sub 2} is accounted for, the increase in the COE is only 14.4%.

  5. r-process in Type II supernovae and the role of direct capture

    SciTech Connect

    Otsuki, K.; Burrows, A.; Martinez-Pinedo, G.; Typel, S.; Langanke, K.; Matos, M.

    2010-06-01

    We have calculated r-process nucleosynthesis based on acoustic wave driven supernova simulation. The environment includes extremely high entropy cases which has not been studied in previous studies. Plenty of actinide and third peak elements are formed in an averaged abundance, while elements around the first and second peaks are overproduced. We also studied the effect of direct capture in r-process. The direct capture furthers r-process and make freeze out earlier. It will change the final abundance drastically. We recalculated r-process nucleosynthesis of the simulation considering the direct capture reaction. While we could not see a significant difference in averaged abundances, significant differences appeared in several individual yields.

  6. Natural materials for carbon capture.

    SciTech Connect

    Myshakin, Evgeniy M.; Romanov, Vyacheslav N.; Cygan, Randall Timothy

    2010-11-01

    Naturally occurring clay minerals provide a distinctive material for carbon capture and carbon dioxide sequestration. Swelling clay minerals, such as the smectite variety, possess an aluminosilicate structure that is controlled by low-charge layers that readily expand to accommodate water molecules and, potentially, carbon dioxide. Recent experimental studies have demonstrated the efficacy of intercalating carbon dioxide in the interlayer of layered clays but little is known about the molecular mechanisms of the process and the extent of carbon capture as a function of clay charge and structure. A series of molecular dynamics simulations and vibrational analyses have been completed to assess the molecular interactions associated with incorporation of CO2 in the interlayer of montmorillonite clay and to help validate the models with experimental observation.

  7. Model based adaptive control of a continuous capture process for monoclonal antibodies production.

    PubMed

    Steinebach, Fabian; Angarita, Monica; Karst, Daniel J; Müller-Späth, Thomas; Morbidelli, Massimo

    2016-04-29

    A two-column capture process for continuous processing of cell-culture supernatant is presented. Similar to other multicolumn processes, this process uses sequential countercurrent loading of the target compound in order maximize resin utilization and productivity for a given product yield. The process was designed using a novel mechanistic model for affinity capture, which takes both specific adsorption as well as transport through the resin beads into account. Simulations as well as experimental results for the capture of an IgG antibody are discussed. The model was able to predict the process performance in terms of yield, productivity and capacity utilization. Compared to continuous capture with two columns operated batch wise in parallel, a 2.5-fold higher capacity utilization was obtained for the same productivity and yield. This results in an equal improvement in product concentration and reduction of buffer consumption. The developed model was used not only for the process design and optimization but also for its online control. In particular, the unit operating conditions are changed in order to maintain high product yield while optimizing the process performance in terms of capacity utilization and buffer consumption also in the presence of changing upstream conditions and resin aging.

  8. Model based adaptive control of a continuous capture process for monoclonal antibodies production.

    PubMed

    Steinebach, Fabian; Angarita, Monica; Karst, Daniel J; Müller-Späth, Thomas; Morbidelli, Massimo

    2016-04-29

    A two-column capture process for continuous processing of cell-culture supernatant is presented. Similar to other multicolumn processes, this process uses sequential countercurrent loading of the target compound in order maximize resin utilization and productivity for a given product yield. The process was designed using a novel mechanistic model for affinity capture, which takes both specific adsorption as well as transport through the resin beads into account. Simulations as well as experimental results for the capture of an IgG antibody are discussed. The model was able to predict the process performance in terms of yield, productivity and capacity utilization. Compared to continuous capture with two columns operated batch wise in parallel, a 2.5-fold higher capacity utilization was obtained for the same productivity and yield. This results in an equal improvement in product concentration and reduction of buffer consumption. The developed model was used not only for the process design and optimization but also for its online control. In particular, the unit operating conditions are changed in order to maintain high product yield while optimizing the process performance in terms of capacity utilization and buffer consumption also in the presence of changing upstream conditions and resin aging. PMID:27046002

  9. Measurement of carbon capture efficiency and stored carbon leakage

    SciTech Connect

    Keeling, Ralph F.; Dubey, Manvendra K.

    2013-01-29

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

  10. The Value of Post-Combustion Carbon Dioxide Capture and Storage Technologies in a World with Uncertain Greenhouse Gas Emissions Constraints

    SciTech Connect

    Wise, Marshall A.; Dooley, James J.

    2009-01-01

    By analyzing how the largest CO2 emitting electricity generating region in the United States, the East Central Area Reliability Coordination Agreement (ECAR), responds to hypothetical constraints on greenhouse gas emissions, the authors demonstrate that there is an enduring role for post combustion CO2 capture technologies. The utilization of pulverized coal with carbon dioxide capture and storage (PC+CCS) technologies is particularly significant in a world where there is significant uncertainty about the future evolution of climate policy and in particular uncertainty about the rate at which the climate policy will become more stringent. The paper’s analysis shows that within this one large, heavily coal-dominated electricity generating region, as much as 20-40 GW of PC+CCS could be in operation before the middle of this century. Depending upon the state of PC+CCS technology development and the evolution of future climate policy, the analysis shows that these CCS systems could be mated to either already existing PC units or PC units that are currently under construction, announced and planned units, as well as PC units that could continue to be built for a number of decades even in the face of a climate policy. In nearly all the cases analyzed here, these PC+CCS generation units are compliments to a much larger deployment of CCS-enabled coal-fired integrated gasification combined cycle (IGCC) power plants. The analysis presented here shows that the combined deployment of PC+CCS and IGCC+CCS units within this one region of the U.S. could result in the potential capture and storage of between 3.2 and 4.9 billion tones of CO2 before the middle of this century in the region’s deep geologic storage formations.

  11. Neutron Capture on 130Sn during r-Process Freeze-Out

    SciTech Connect

    Beun, Joshua; Blackmon, Jeffery C; Hix, William Raphael; Mclaughlin, Gail C; Smith, Michael Scott; Surman, Rebecca

    2009-01-01

    We examine the role of neutron capture on {sup 130}Sn during r-process freeze-out in the neutrino-driven wind environment of the core-collapse supernova. We find that the global r-process abundance pattern is sensitive to the magnitude of the neutron capture cross section of {sup 130}Sn. The changes to the abundance pattern include not only a relative decrease in the abundance of {sup 130}Sn and an increase in the abundance of {sup 131}Sn, but also a shift in the distribution of material in the rare earth and third peak regions.

  12. Carbon capture and biogas enhancement by carbon dioxide enrichment of anaerobic digesters treating sewage sludge or food waste.

    PubMed

    Bajón Fernández, Y; Soares, A; Villa, R; Vale, P; Cartmell, E

    2014-05-01

    The increasing concentration of carbon dioxide (CO2) in the atmosphere and the stringent greenhouse gases (GHG) reduction targets, require the development of CO2 sequestration technologies applicable for the waste and wastewater sector. This study addressed the reduction of CO2 emissions and enhancement of biogas production associated with CO2 enrichment of anaerobic digesters (ADs). The benefits of CO2 enrichment were examined by injecting CO2 at 0, 0.3, 0.6 and 0.9 M fractions into batch ADs treating food waste or sewage sludge. Daily specific methane (CH4) production increased 11-16% for food waste and 96-138% for sewage sludge over the first 24h. Potential CO2 reductions of 8-34% for sewage sludge and 3-11% for food waste were estimated. The capacity of ADs to utilise additional CO2 was demonstrated, which could provide a potential solution for onsite sequestration of CO2 streams while enhancing renewable energy production.

  13. Tubular ceramic-supported sol-gel silica-based membranes for flue gas carbon dioxide capture and sequestration.

    SciTech Connect

    Tsai, C. Y.; Xomeritakis, George K.; Brinker, C. Jeffrey; Jiang, Ying-Bing

    2009-03-01

    Pure, amine-derivatized and nickel-doped sol-gel silica membranes have been developed on tubular Membralox-type commercial ceramic supports for the purpose of carbon dioxide separation from nitrogen under coal-fired power plant flue gas conditions. An extensive synthetic and permeation test study was carried out in order to optimize membrane CO{sub 2} permeance, CO{sub 2}:N{sub 2} separation factor and resistance against densification. Pure silica membranes prepared under optimized conditions exhibited an attractive combination of CO{sub 2} permeance of 2.0 MPU (1 MPU = 1 cm{sup 3}(STP) {center_dot} cm{sup -2} min{sup -1} atm{sup -1}) and CO{sub 2}:N{sub 2} separation factor of 80 with a dry 10:90 (v/v) CO{sub 2}:N{sub 2} feed at 25 C. However, these membranes exhibited flux decline phenomena under prolonged exposure to humidified feeds, especially in the presence of trace SO{sub 2} gas in the feed. Doping the membranes with nickel (II) nitrate salt was effective in retarding densification, as manifested by combined higher permeance and higher separation factor of the doped membrane compared to the pure (undoped) silica membrane after 168 hours exposure to simulated flue gas conditions.

  14. Carbon dioxide pressure swing adsorption process using modified alumina adsorbents

    DOEpatents

    Gaffney, T.R.; Golden, T.C.; Mayorga, S.G.; Brzozowski, J.R.; Taylor, F.W.

    1999-06-29

    A pressure swing adsorption process for absorbing CO[sub 2] from a gaseous mixture containing CO[sub 2] comprises introducing the gaseous mixture at a first pressure into a reactor containing a modified alumina adsorbent maintained at a temperature ranging from 100 C and 500 C to adsorb CO[sub 2] to provide a CO[sub 2] laden alumina adsorbent and a CO[sub 2] depleted gaseous mixture and contacting the CO[sub 2] laden adsorbent with a weakly adsorbing purge fluid at a second pressure which is lower than the first pressure to desorb CO[sub 2] from the CO[sub 2] laden alumina adsorbent. The modified alumina adsorbent which is formed by depositing a solution having a pH of 3.0 or more onto alumina and heating the alumina to a temperature ranging from 100 C and 600 C, is not degraded by high concentrations of water under process operating conditions. 1 fig.

  15. Carbon dioxide pressure swing adsorption process using modified alumina adsorbents

    DOEpatents

    Gaffney, Thomas Richard; Golden, Timothy Christopher; Mayorga, Steven Gerard; Brzozowski, Jeffrey Richard; Taylor, Fred William

    1999-01-01

    A pressure swing adsorption process for absorbing CO.sub.2 from a gaseous mixture containing CO.sub.2 comprising introducing the gaseous mixture at a first pressure into a reactor containing a modified alumina adsorbent maintained at a temperature ranging from 100.degree. C. and 500.degree. C. to adsorb CO.sub.2 to provide a CO.sub.2 laden alumina adsorbent and a CO.sub.2 depleted gaseous mixture and contacting the CO.sub.2 laden adsorbent with a weakly adsorbing purge fluid at a second pressure which is lower than the first pressure to desorb CO.sub.2 from the CO.sub.2 laden alumina adsorbent. The modified alumina adsorbent which is formed by depositing a solution having a pH of 3.0 or more onto alumina and heating the alumina to a temperature ranging from 100.degree. C. and 600.degree. C., is not degraded by high concentrations of water under process operating conditions.

  16. Large-Scale Utilization of Biomass Energy and Carbon Dioxide Capture and Storage in the Transport and Electricity Sectors under Stringent CO2 Concentration Limit Scenarios

    SciTech Connect

    Luckow, Patrick; Wise, Marshall A.; Dooley, James J.; Kim, Son H.

    2010-08-05

    This paper examines the potential role of large scale, dedicated commercial biomass energy systems under global climate policies designed to meet atmospheric concentrations of CO2 at 400ppm and 450ppm by the end of the century. We use an integrated assessment model of energy and agriculture systems to show that, given a climate policy in which terrestrial carbon is appropriately valued equally with carbon emitted from the energy system, biomass energy has the potential to be a major component of achieving these low concentration targets. A key aspect of the research presented here is that the costs of processing and transporting biomass energy at much larger scales than current experience are explicitly incorporated into the modeling. From the scenario results, 120-160 EJ/year of biomass energy is produced globally by midcentury and 200-250 EJ/year by the end of this century. In the first half of the century, much of this biomass is from agricultural and forest residues, but after 2050 dedicated cellulosic biomass crops become the majority source, along with growing utilization of waste-to-energy. The ability to draw on a diverse set of biomass based feedstocks helps to reduce the pressure for drastic large-scale changes in land use and the attendant environmental, ecological, and economic consequences those changes would unleash. In terms of the conversion of bioenergy feedstocks into value added energy, this paper demonstrates that biomass is and will continue to be used to generate electricity as well as liquid transportation fuels. A particular focus of this paper is to show how climate policies and technology assumptions - especially the availability of carbon dioxide capture and storage (CCS) technologies - affect the decisions made about where the biomass is used in the energy system. The potential for net-negative electric sector emissions through the use of CCS with biomass feedstocks provides an attractive part of the solution for meeting stringent

  17. Comparative assessment of status and opportunities for carbon Dioxide Capture and storage and Radioactive Waste Disposal In North America

    SciTech Connect

    Oldenburg, C.; Birkholzer, J.T.

    2011-07-22

    Aside from the target storage regions being underground, geologic carbon sequestration (GCS) and radioactive waste disposal (RWD) share little in common in North America. The large volume of carbon dioxide (CO{sub 2}) needed to be sequestered along with its relatively benign health effects present a sharp contrast to the limited volumes and hazardous nature of high-level radioactive waste (RW). There is well-documented capacity in North America for 100 years or more of sequestration of CO{sub 2} from coal-fired power plants. Aside from economics, the challenges of GCS include lack of fully established legal and regulatory framework for ownership of injected CO{sub 2}, the need for an expanded pipeline infrastructure, and public acceptance of the technology. As for RW, the USA had proposed the unsaturated tuffs of Yucca Mountain, Nevada, as the region's first high-level RWD site before removing it from consideration in early 2009. The Canadian RW program is currently evolving with options that range from geologic disposal to both decentralized and centralized permanent storage in surface facilities. Both the USA and Canada have established legal and regulatory frameworks for RWD. The most challenging technical issue for RWD is the need to predict repository performance on extremely long time scales (10{sup 4}-10{sup 6} years). While attitudes toward nuclear power are rapidly changing as fossil-fuel costs soar and changes in climate occur, public perception remains the most serious challenge to opening RW repositories. Because of the many significant differences between RWD and GCS, there is little that can be shared between them from regulatory, legal, transportation, or economic perspectives. As for public perception, there is currently an opportunity to engage the public on the benefits and risks of both GCS and RWD as they learn more about the urgent energy-climate crisis created by greenhouse gas emissions from current fossil-fuel combustion practices.

  18. New Neutron-capture Measurements in 23 Open Clusters. I. The r-Process

    NASA Astrophysics Data System (ADS)

    Overbeek, Jamie C.; Friel, Eileen D.; Jacobson, Heather R.

    2016-06-01

    Neutron-capture elements, those with Z > 35, are the least well understood in terms of nucleosynthesis and formation environments. The rapid neutron-capture, or r-process, elements are formed in the environments and/or remnants of massive stars, while the slow neutron-capture, or s-process, elements are primarily formed in low-mass AGB stars. These elements can provide much information about Galactic star formation and enrichment, but observational data are limited. We have assembled a sample of 68 stars in 23 open clusters that we use to probe abundance trends for six neutron-capture elements (Eu, Gd, Dy, Mo, Pr, and Nd) with cluster age and location in the disk of the Galaxy. In order to keep our analysis as homogeneous as possible, we use an automated synthesis fitting program, which also enables us to measure multiple (3-10) lines for each element. We find that the pure r-process elements (Eu, Gd, and Dy) have positive trends with increasing cluster age, while the mixed r- and s-process elements (Mo, Pr, and Nd) have insignificant trends consistent with zero. Pr, Nd, Eu, Gd, and Dy have similar, slight (although mostly statistically significant) gradients of ˜0.04 dex kpc-1. The mixed elements also appear to have nonlinear relationships with R GC.

  19. New Neutron-capture Measurements in 23 Open Clusters. I. The r-Process

    NASA Astrophysics Data System (ADS)

    Overbeek, Jamie C.; Friel, Eileen D.; Jacobson, Heather R.

    2016-06-01

    Neutron-capture elements, those with Z > 35, are the least well understood in terms of nucleosynthesis and formation environments. The rapid neutron-capture, or r-process, elements are formed in the environments and/or remnants of massive stars, while the slow neutron-capture, or s-process, elements are primarily formed in low-mass AGB stars. These elements can provide much information about Galactic star formation and enrichment, but observational data are limited. We have assembled a sample of 68 stars in 23 open clusters that we use to probe abundance trends for six neutron-capture elements (Eu, Gd, Dy, Mo, Pr, and Nd) with cluster age and location in the disk of the Galaxy. In order to keep our analysis as homogeneous as possible, we use an automated synthesis fitting program, which also enables us to measure multiple (3–10) lines for each element. We find that the pure r-process elements (Eu, Gd, and Dy) have positive trends with increasing cluster age, while the mixed r- and s-process elements (Mo, Pr, and Nd) have insignificant trends consistent with zero. Pr, Nd, Eu, Gd, and Dy have similar, slight (although mostly statistically significant) gradients of ˜0.04 dex kpc‑1. The mixed elements also appear to have nonlinear relationships with R GC.

  20. State-of-the-art adsorption and membrane separation processes for carbon dioxide production from carbon dioxide emitting industries

    SciTech Connect

    Ebner, A.D.; Ritter, J.A.

    2009-07-01

    With the growing concern about global warming placing greater demands on improving energy efficiency and reducing CO{sub 2} emissions, the need for improving the energy intensive, separation processes involving CO{sub 2} is well recognized. The US Department of Energy estimates that the separation of CO{sub 2} represents 75% of the cost associated with its separation, storage, transport, and sequestration operations. Hence, energy efficient, CO{sub 2} separation technologies with improved economics are needed for industrial processing and for future options to capture and concentrate CO{sub 2} for reuse or sequestration. The overall goal of this review is to foster the development of new adsorption and membrane technologies to improve manufacturing efficiency and reduce CO{sub 2} emissions. This study focuses on the power, petrochemical, and other CO{sub 2} emitting industries, and provides a detailed review of the current commercial CO{sub 2} separation technologies, i.e., absorption, adsorption, membrane, and cryogenic, an overview of the emerging adsorption and membrane technologies for CO{sub 2} separation, and both near and long term recommendations for future research on adsorption and membrane technologies. Flow sheets of the principal CO{sub 2} producing processes are provided for guidance and new conceptual flow sheets with ideas on the placement of CO{sub 2} separations technologies have also been devised.

  1. Capturing exponential variance using polynomial resources: applying tensor networks to nonequilibrium stochastic processes.

    PubMed

    Johnson, T H; Elliott, T J; Clark, S R; Jaksch, D

    2015-03-01

    Estimating the expected value of an observable appearing in a nonequilibrium stochastic process usually involves sampling. If the observable's variance is high, many samples are required. In contrast, we show that performing the same task without sampling, using tensor network compression, efficiently captures high variances in systems of various geometries and dimensions. We provide examples for which matching the accuracy of our efficient method would require a sample size scaling exponentially with system size. In particular, the high-variance observable e^{-βW}, motivated by Jarzynski's equality, with W the work done quenching from equilibrium at inverse temperature β, is exactly and efficiently captured by tensor networks.

  2. Review of measurement techniques for the neutron radiative-capture process

    SciTech Connect

    Poenitz, W.P.

    1981-07-01

    The experimental techniques applied in measurements of the neutron capture process are reviewed. The emphasis is on measurement techniques used in neutron capture cross section measurements. The activation technique applied mainly in earlier work has still its use in some cases, specifically for measurements of technologically important cross sections (/sup 238/U and /sup 232/Th) with high accuracy. Three major prompt neutron radioactive capture detection techniques have evolved: the total gamma radiation energy detection technique (mainly with large liquid scintillation detectors), the gamma-energy proportional detectors (with proportional counters or Moxon-Rae detectors), and the pulse-height weighting technique. These measurement techniques are generally applicable, however, shortcomings limit the achievable accuracy to a approx. = 5 to 15% uncertainty level.

  3. Enriching blast furnace gas by removing carbon dioxide.

    PubMed

    Zhang, Chongmin; Sun, Zhimin; Chen, Shuwen; Wang, Baohai

    2013-12-01

    Blast furnace gas (BF gas) produced in the iron making process is an essential energy resource for a steel making work. As compared with coke oven gas, the caloric value of BF gas is too low to be used alone as fuel in hot stove because of its high concentrations of carbon dioxide and nitrogen. If the carbon dioxide in BF gas could be captured efficiently, it would meet the increasing need of high caloric BF gas, and develop methods to reusing and/or recycling the separated carbon dioxide further. Focused on this, investigations were done with simple evaluation on possible methods of removing carbon dioxide from BF gas and basic experiments on carbon dioxide capture by chemical absorption. The experimental results showed that in 100 minutes, the maximum absorbed doses of carbon dioxide reached 20 g/100 g with ionic liquid as absorbent.

  4. Solid phase extraction with silicon dioxide microsphere adsorbents in combination with gas chromatography-electron capture detection for the determination of DDT and its metabolites in water samples.

    PubMed

    Zhou, Qingxiang; Wu, Wei; Xie, Guohong

    2013-01-01

    The goal of the present study was to investigate the feasibility of silicon dioxide (SiO(2)) microspheres without special modification to enrich dichlorodiphenyltrichloroethane (DDT) and its main metabolites, p,p'-dichlorodiphenyl-2,2-dichloroethylene (p,p'-DDD) and p,p'-dichlorodiphenyldichloroethylene (DDE) in combination with gas chromatography-electron-capture detection. The experimental results indicated that an excellent linear relationship between the recoveries and the concentrations of DDT and its main metabolites was obtained in the range of 0.2-30 ng mL(-1) and the correlation coefficients were in the range of 99.96-99.99%. The detection limits based on the ratio of signal to the baseline noise (S/N = 3) were 2.2, 2.9, 3.8 and 4.1 ng L(-1) for p,p'-DDD, p,p'-DDT, o,p'-DDT, and p,p'-DDE, respectively. The precisions of the proposed method were all below 10% (n = 6). Four real water samples were utilized for validation of the proposed method, and satisfactory spiked recoveries in the range of 72.4-112.9% were achieved. These results demonstrated that the developed method was a simple, sensitive, and robust analytical method for the monitoring of pollutants in the environment. PMID:23356340

  5. Solid phase extraction with silicon dioxide microsphere adsorbents in combination with gas chromatography-electron capture detection for the determination of DDT and its metabolites in water samples.

    PubMed

    Zhou, Qingxiang; Wu, Wei; Xie, Guohong

    2013-01-01

    The goal of the present study was to investigate the feasibility of silicon dioxide (SiO(2)) microspheres without special modification to enrich dichlorodiphenyltrichloroethane (DDT) and its main metabolites, p,p'-dichlorodiphenyl-2,2-dichloroethylene (p,p'-DDD) and p,p'-dichlorodiphenyldichloroethylene (DDE) in combination with gas chromatography-electron-capture detection. The experimental results indicated that an excellent linear relationship between the recoveries and the concentrations of DDT and its main metabolites was obtained in the range of 0.2-30 ng mL(-1) and the correlation coefficients were in the range of 99.96-99.99%. The detection limits based on the ratio of signal to the baseline noise (S/N = 3) were 2.2, 2.9, 3.8 and 4.1 ng L(-1) for p,p'-DDD, p,p'-DDT, o,p'-DDT, and p,p'-DDE, respectively. The precisions of the proposed method were all below 10% (n = 6). Four real water samples were utilized for validation of the proposed method, and satisfactory spiked recoveries in the range of 72.4-112.9% were achieved. These results demonstrated that the developed method was a simple, sensitive, and robust analytical method for the monitoring of pollutants in the environment.

  6. Advanced computational tools for optimization and uncertainty quantification of carbon capture processes

    SciTech Connect

    Miller, David C.; Ng, Brenda; Eslick, John

    2014-01-01

    Advanced multi-scale modeling and simulation has the potential to dramatically reduce development time, resulting in considerable cost savings. The Carbon Capture Simulation Initiative (CCSI) is a partnership among national laboratories, industry and universities that is developing, demonstrating, and deploying a suite of multi-scale modeling and simulation tools. One significant computational tool is FOQUS, a Framework for Optimization and Quantification of Uncertainty and Sensitivity, which enables basic data submodels, including thermodynamics and kinetics, to be used within detailed process models to rapidly synthesize and optimize a process and determine the level of uncertainty associated with the resulting process. The overall approach of CCSI is described with a more detailed discussion of FOQUS and its application to carbon capture systems.

  7. Anion production in high-velocity cluster-atom collisions; the electron capture process revisited

    NASA Astrophysics Data System (ADS)

    Béroff, K.; Chabot, M.; Martinet, G.; Pino, T.; Bouneau, S.; Le Padellec, A.; Féraud, G.; Do Thi, N.; Calvo, F.; Bordas, C.; Lépine, F.

    2013-01-01

    Anion production cross sections in collisions between Cn+, Cn carbon clusters (n ≤ 5) and helium atoms have been measured in high-velocity collisions (v = 2.25 and 2.6 au). This paper focuses on two of the three processes responsible for the Cn- production, namely double electron capture (DEC) onto Cn+ cations and single electron capture onto neutral (SECN) Cn. They were experimentally distinguished from a gaseous thickness dependence study. Dissociative and non-dissociative cross sections were measured and, in the case of DEC, all dissociative branching ratios measured; for these small systems, the C2- fragment was found magical. Data concerning electron capture in neutral-neutral collisions are extremely rare, especially at high velocity. Introduction of this measured process in the independent atom and electron (IAE) model allowed us to revisit and satisfactorily reproduce the so-far unexplained size evolution of single electron capture (SEC) cross sections in 2.6 au Cn+-He (n ≤ 10) collisions (Chabot et al 2006 J. Phys. B: At. Mol. Opt. Phys. 39 2593-603). IAE calculations for DEC cross sections and their comparison with experiment suggest a loss of electron in anionic Cn- species after the collision, competing with fragmentation and depending on the size.

  8. Electron capture and excitation processes in H+‑H collisions in dense quantum plasmas

    NASA Astrophysics Data System (ADS)

    Jakimovski, D.; Markovska, N.; Janev, R. K.

    2016-10-01

    Electron capture and excitation processes in proton–hydrogen atom collisions taking place in dense quantum plasmas are studied by employing the two-centre atomic orbital close-coupling (TC-AOCC) method. The Debye–Hückel cosine (DHC) potential is used to describe the plasma screening effects on the Coulomb interaction between charged particles. The properties of a hydrogen atom with DHC potential are investigated as a function of the screening strength of the potential. It is found that the decrease in binding energy of nl levels with increasing screening strength is considerably faster than in the case of the Debye–Hückel (DH) screening potential, appropriate for description of charged particle interactions in weakly coupled classical plasmas. This results in a reduction in the number of bound states in the DHC potential with respect to that in the DH potential for the same plasma screening strength, and is reflected in the dynamics of excitation and electron capture processes for the two screened potentials. The TC-AOCC cross sections for total and state-selective electron capture and excitation cross sections with the DHC potential are calculated for a number of representative screening strengths in the 1–300 keV energy range and compared with those for the DH and pure Coulomb potential. The total capture cross sections for a selected number of screening strengths are compared with the available results from classical trajectory Monte Carlo calculations.

  9. Post-AGB stars in the Magellanic Clouds and neutron-capture processes in AGB stars

    NASA Astrophysics Data System (ADS)

    Lugaro, M.; Campbell, S. W.; Van Winckel, H.; De Smedt, K.; Karakas, A. I.; Käppeler, F.

    2015-11-01

    Aims: We explore modifications to the current scenario for the slow neutron-capture process (the s-process) in asymptotic giant branch (AGB) stars to account for the Pb deficiency observed in post-AGB stars of low metallicity ([Fe/H] ≃-1.2) and low initial mass (≃ 1-1.5 M⊙) in the Large and Small Magellanic Clouds. Methods: We calculated the stellar evolution and nucleosynthesis for a 1.3 M⊙ star with [Fe/H] = -1.3 and tested different amounts and distributions of protons leading to the production of the main neutron source within the 13C-pocket and proton ingestion scenarios. Results: No s-process models can fully reproduce the abundance patterns observed in the post-AGB stars. When the Pb production is lowered, the abundances of the elements between Eu and Pb, such as Er, Yb, W, and Hf, are also lowered to below those observed. Conclusions: Neutron-capture processes with neutron densities intermediate between the s and the rapid neutron-capture processes may provide a solution to this problem and be a common occurrence in low-mass, low-metallicity AGB stars.

  10. Carbon dioxide absorbent and method of using the same

    SciTech Connect

    Perry, Robert James; O'Brien, Michael Joseph

    2014-06-10

    In accordance with one aspect, the present invention provides a composition which contains the amino-siloxane structures I, or III, as described herein. The composition is useful for the capture of carbon dioxide from process streams. In addition, the present invention provides methods of preparing the amino-siloxane composition. Another aspect of the present invention provides methods for reducing the amount of carbon dioxide in a process stream employing the amino-siloxane compositions of the invention, as species which react with carbon dioxide to form an adduct with carbon dioxide.

  11. Carbon dioxide absorbent and method of using the same

    SciTech Connect

    Perry, Robert James; O'Brien, Michael Joseph

    2015-12-29

    In accordance with one aspect, the present invention provides a composition which contains the amino-siloxane structures I, or III, as described herein. The composition is useful for the capture of carbon dioxide from process streams. In addition, the present invention provides methods of preparing the amino-siloxane composition. Another aspect of the present invention provides methods for reducing the amount of carbon dioxide in a process stream employing the amino-siloxane compositions of the invention, as species which react with carbon dioxide to form an adduct with carbon dioxide.

  12. Design of Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

    SciTech Connect

    Wood, Benjamin

    2012-06-30

    The major goal of the project is to design and optimize a bench-scale process for novel silicone CO{sub 2}-capture solvents and establish scalability and potential for commercialization of post-combustion capture of CO{sub 2} from coal-fired power plants. This system should be capable of 90% capture efficiency and demonstrate that less than 35% increase in the cost of energy services can be achieved upon scale-up. Experiments were conducted to obtain data required for design of the major unit operations. The bench-scale system design has been completed, including sizing of major unit operations and the development of a detailed Process and Instrument Diagram (P&ID). The system has been designed to be able to operate over a wide range of process conditions so that the effect of various process variables on performance can be determined. To facilitate flexibility in operation, the absorption column has been designed in a modular manner, so that the height of the column can be varied. The desorber has also been designed to allow for a range of residence times, temperatures, and pressures. The system will be fabricated at Techniserv Inc.

  13. Neutron Capture Rates near A=130 which Effect a Global Change to the r-Process Abundance Distribution

    SciTech Connect

    Surman, Rebecca; Beun, Joshua; Mclaughlin, Gail C; Hix, William Raphael

    2009-01-01

    We investigate the impact of neutron capture rates near the A=130 peak on the r-process abundance pattern. We show that these capture rates can alter the abundances of individual nuclear species, not only in the region of A=130 peak but also throughout the abundance pattern. We discuss in general the nonequilibrium processes that produce these abundance changes and determine which capture rates have the most significant impact.

  14. Geologic Sequestration of Carbon Dioxide

    NASA Astrophysics Data System (ADS)

    Benson, S. M.

    2003-04-01

    Geologic sequestration of carbon dioxide has emerged as one of the most promising options for making deep cuts in carbon dioxide emissions. Geologic sequestration involves the two-step process of first capturing carbon dioxide by separating it from stack emissions, followed by injection and long term storage in deep geologic formations. Sedimentary basins, including depleted oil and gas reservoirs, deep unminable coal seams, and brine-filled formations, provide the most attractive storage reservoirs. Over the past few years significant advances have been made in this technology, including development of simulation models and monitoring systems, implementation of commercial scale demonstration projects, and investigation of natural and industrial analogues for geologic storage of carbon dioxide. While much has been accomplished in a short time, there are many questions that must be answered before this technology can be employed on the scale needed to make significant reductions in carbon dioxide emissions. Questions such as how long must the carbon dioxide remain underground, to what extent will geochemical reactions completely immobilize the carbon dioxide, what can be done in the event that a storage site begins to leak at an unacceptable rate, what is the appropriate risk assessment, regulatory and legal framework, and will the public view this option favorably? This paper will present recent advances in the scientific and technological underpinnings of geologic sequestration and identify areas where additional information is needed.

  15. The Processing of Image Data Collected by Light UAV Systems for GIS Data Capture and Updating

    NASA Astrophysics Data System (ADS)

    Yastikli, N.; Bagci, I.; Beser, C.

    2013-10-01

    The collection and updating of 3D data is the one of the important steps for GIS applications which require fast and efficient data collection methods. The photogrammetry has been used for many years as a data collection method for GIS application in larger areas. The Unmanned Aerial Vehicles (UAV) Systems gained increasing attraction in geosciences for cost effective data capture and updating at high spatial and temporal resolution during the last years. These autonomously flying UAV systems are usually equipped with different sensors such as GPS receiver, microcomputers, gyroscopes and miniaturized sensor systems for navigation, positioning, and mapping purposes. The UAV systems can be used for data collection for digital elevation model DEM and orthoimages generation in GIS application at small areas. In this study, data collection and processing by light UAV system will be evaluated for GIS data capture and updating for small areas where not feasible for traditional photogrammetry. The main aim of this study is to design the low cost light UAV system for GIS data capture and update. The investigation was based on the aerial images which recorded during the flights performed with UAV system over the test site in Davutpasa Campus of Yildiz Technical University, Istanbul. The quality of generated DEM and ortho-images from UAV flights was discussed for GIS data capture and updating for small areas.

  16. Pre-Combustion Carbon Capture by a Nanoporous, Superhydrophobic Membrane Contactor Process

    SciTech Connect

    Meyer, Howard; Zhou, S James; Ding, Yong; Bikson, Ben

    2012-03-31

    This report summarizes progress made during Phase I and Phase II of the project: "Pre-Combustion Carbon Capture by a Nanoporous, Superhydrophobic Membrane Contactor Process," under contract DE-FE-0000646. The objective of this project is to develop a practical and cost effective technology for CO{sub 2} separation and capture for pre-combustion coal-based gasification plants using a membrane contactor/solvent absorption process. The goals of this technology development project are to separate and capture at least 90% of the CO{sub 2} from Integrated Gasification Combined Cycle (IGCC) power plants with less than 10% increase in the cost of energy services. Unlike conventional gas separation membranes, the membrane contactor is a novel gas separation process based on the gas/liquid membrane concept. The membrane contactor is an advanced mass transfer device that operates with liquid on one side of the membrane and gas on the other. The membrane contactor can operate with pressures that are almost the same on both sides of the membrane, whereas the gas separation membranes use the differential pressure across the membrane as driving force for separation. The driving force for separation for the membrane contactor process is the chemical potential difference of CO{sub 2} in the gas phase and in the absorption liquid. This process is thus easily tailored to suit the needs for pre-combustion separation and capture of CO{sub 2}. Gas Technology Institute (GTI) and PoroGen Corporation (PGC) have developed a novel hollow fiber membrane technology that is based on chemically and thermally resistant commercial engineered polymer poly(ether ether ketone) or PEEK. The PEEK membrane material used in the membrane contactor during this technology development program is a high temperature engineered plastic that is virtually non-destructible under the operating conditions encountered in typical gas absorption applications. It can withstand contact with most of the common treating

  17. Advanced Amine Solvent Formulations and Process Integration for Near-Term CO2 Capture Success

    SciTech Connect

    Fisher, Kevin S.; Searcy, Katherine; Rochelle, Gary T.; Ziaii, Sepideh; Schubert, Craig

    2007-06-28

    This Phase I SBIR project investigated the economic and technical feasibility of advanced amine scrubbing systems for post-combustion CO2 capture at coal-fired power plants. Numerous combinations of advanced solvent formulations and process configurations were screened for energy requirements, and three cases were selected for detailed analysis: a monoethanolamine (MEA) base case and two “advanced” cases: an MEA/Piperazine (PZ) case, and a methyldiethanolamine (MDEA) / PZ case. The MEA/PZ and MDEA/PZ cases employed an advanced “double matrix” stripper configuration. The basis for calculations was a model plant with a gross capacity of 500 MWe. Results indicated that CO2 capture increased the base cost of electricity from 5 cents/kWh to 10.7 c/kWh for the MEA base case, 10.1 c/kWh for the MEA / PZ double matrix, and 9.7 c/kWh for the MDEA / PZ double matrix. The corresponding cost per metric tonne CO2 avoided was 67.20 $/tonne CO2, 60.19 $/tonne CO2, and 55.05 $/tonne CO2, respectively. Derated capacities, including base plant auxiliary load of 29 MWe, were 339 MWe for the base case, 356 MWe for the MEA/PZ double matrix, and 378 MWe for the MDEA / PZ double matrix. When compared to the base case, systems employing advanced solvent formulations and process configurations were estimated to reduce reboiler steam requirements by 20 to 44%, to reduce derating due to CO2 capture by 13 to 30%, and to reduce the cost of CO2 avoided by 10 to 18%. These results demonstrate the potential for significant improvements in the overall economics of CO2 capture via advanced solvent formulations and process configurations.

  18. Investigation of Ester- and Amide-Linker-Based Porous Organic Polymers for Carbon Dioxide Capture and Separation at Wide Temperatures and Pressures.

    PubMed

    Ullah, Ruh; Atilhan, Mert; Anaya, Baraa; Al-Muhtaseb, Shaheen; Aparicio, Santiago; Patel, Hasmukh; Thirion, Damien; Yavuz, Cafer T

    2016-08-17

    Organic compounds, such as covalent organic framework, metal-organic frameworks, and covalent organic polymers have been under investigation to replace the well-known amine-based solvent sorption technology of CO2 and introduce the most efficient and economical material for CO2 capture and storage. Various organic polymers having different function groups have been under investigation both for low and high pressure CO2 capture. However, search for a promising material to overcome the issues of lower selectivity, less capturing capacity, lower mass transfer coefficient and instability in materials performance at high pressure and various temperatures is still ongoing process. Herein, we report synthesis of six covalent organic polymers (COPs) and their CO2, N2, and CH4 adsorption performances at low and high pressures up to 200 bar. All the presented COPs materials were characterized by using elemental analysis method, Fourier transform infrared spectroscopy (FTIR) and solid state nuclear magnetic resonance (NMR) spectroscopy techniques. Physical properties of the materials such as surface areas, pore volume and pore size were determined through BET analysis at 77 K. All the materials were tested for CO2, CH4, and N2 adsorption using state of the art equipment, magnetic suspension balance (MSB). Results indicated that, amide based material i.e. COP-33 has the largest pore volume of 0.2 cm(2)/g which can capture up to the maximum of 1.44 mmol/g CO2 at room temperature and at pressure of 10 bar. However, at higher pressure of 200 bar and 308 K ester-based compound, that is, COP-35 adsorb as large as 144 mmol/g, which is the largest gas capturing capacity of any COPs material obtained so far. Importantly, single gas measurement based selectivity of COP-33 was comparatively better than all other COPs materials at all condition. Nevertheless, overall performance of COP-35 rate of adsorption and heat of adsorption has indicated that this material can be considered for

  19. Investigation of Ester- and Amide-Linker-Based Porous Organic Polymers for Carbon Dioxide Capture and Separation at Wide Temperatures and Pressures.

    PubMed

    Ullah, Ruh; Atilhan, Mert; Anaya, Baraa; Al-Muhtaseb, Shaheen; Aparicio, Santiago; Patel, Hasmukh; Thirion, Damien; Yavuz, Cafer T

    2016-08-17

    Organic compounds, such as covalent organic framework, metal-organic frameworks, and covalent organic polymers have been under investigation to replace the well-known amine-based solvent sorption technology of CO2 and introduce the most efficient and economical material for CO2 capture and storage. Various organic polymers having different function groups have been under investigation both for low and high pressure CO2 capture. However, search for a promising material to overcome the issues of lower selectivity, less capturing capacity, lower mass transfer coefficient and instability in materials performance at high pressure and various temperatures is still ongoing process. Herein, we report synthesis of six covalent organic polymers (COPs) and their CO2, N2, and CH4 adsorption performances at low and high pressures up to 200 bar. All the presented COPs materials were characterized by using elemental analysis method, Fourier transform infrared spectroscopy (FTIR) and solid state nuclear magnetic resonance (NMR) spectroscopy techniques. Physical properties of the materials such as surface areas, pore volume and pore size were determined through BET analysis at 77 K. All the materials were tested for CO2, CH4, and N2 adsorption using state of the art equipment, magnetic suspension balance (MSB). Results indicated that, amide based material i.e. COP-33 has the largest pore volume of 0.2 cm(2)/g which can capture up to the maximum of 1.44 mmol/g CO2 at room temperature and at pressure of 10 bar. However, at higher pressure of 200 bar and 308 K ester-based compound, that is, COP-35 adsorb as large as 144 mmol/g, which is the largest gas capturing capacity of any COPs material obtained so far. Importantly, single gas measurement based selectivity of COP-33 was comparatively better than all other COPs materials at all condition. Nevertheless, overall performance of COP-35 rate of adsorption and heat of adsorption has indicated that this material can be considered for

  20. Fused salt processing of impure plutonium dioxide to high-purity plutonium metal

    SciTech Connect

    Mullins, L.J.; Christensen, D.C.; Babcock, B.R.

    1982-01-01

    A process for converting impure plutonium dioxide (approx. 96% pure) to high-purity plutonium metal (>99.9%) was developed. The process consists of reducing the oxide to an impure plutonium metal intermediate with calcium metal in molten calcium chloride. The impure intermediate metal is cast into an anode and electrorefined to produce high-purity plutonium metal. The oxide reduction step is being done now on a 0.6-kg scale with the resulting yield being >99.5%. The electrorefining is being done on a 4.0-kg scale with the resulting yield being 80 to 85%. The purity of the product, which averages 99.98%, is essentially insensitive to the purity of the feed metal. The yield, however, is directly dependent on the chemical composition of the feed. To date, approximately 250 kg of impure oxide has been converted to pure metal by this processing sequence. The availability of impure plutonium dioxide, together with the need for pure plutonium metal, makes this sequence a valuable plutonium processing tool.

  1. Advanced Oxyfuel Boilers and Process Heaters for Cost Effective CO2 Capture and Sequestration

    SciTech Connect

    Max Christie; Rick Victor; Bart van Hassel; Nagendra Nagabushana; Juan Li; Joseph Corpus; Jamie Wilson

    2007-03-31

    The purpose of the advanced boilers and process heaters program is to assess the feasibility of integrating Oxygen Transport Membranes (OTM) into combustion processes for cost effective CO{sub 2} capture and sequestration. Introducing CO{sub 2} capture into traditional combustion processes can be expensive, and the pursuit of alternative methods, like the advanced boiler/process heater system, may yield a simple and cost effective solution. In order to assess the integration of an advanced boiler/process heater process, this program addressed the following tasks: Task 1--Conceptual Design; Task 2--Laboratory Scale Evaluation; Task 3--OTM Development; Task 4--Economic Evaluation and Commercialization Planning; and Task 5--Program Management. This Final report documents and summarizes all of the work performed for the DOE award DE-FC26-01NT41147 during the period from January 2002-March 2007. This report outlines accomplishments for the following tasks: conceptual design and economic analysis, oxygen transport membrane (OTM) development, laboratory scale evaluations, and program management.

  2. Bench Scale Development and Testing of a Novel Adsorption Process for Post-Combustion CO₂ Capture

    SciTech Connect

    Jain, Ravi

    2015-09-01

    A physical sorption process to produce dry CO₂ at high purity (>98%) and high recovery (>90%) from the flue gas taken before or after the FGD was demonstrated both in the lab and in the field (one ton per day scale). A CO₂ recovery of over 94% and a CO₂ purity of over 99% were obtained in the field tests. The process has a moisture, SOX, and Hg removal stage followed by a CO₂ adsorption stage. Evaluations based on field testing, process simulation and detailed engineering studies indicate that the process has the potential for more than 40% reduction in the capital and more than 40% reduction in parasitic power for CO₂ capture compared to MEA. The process has the potential to provide CO₂ at a cost (<$40/tonne) and quality (<1 ppm H₂O, <1 ppm SOX, <10 ppm O₂) suitable for EOR applications which can make CO₂ capture profitable even in the absence of climate legislation. The process is applicable to power plants without SOX, Hg and NOX removal equipment.

  3. Neutron capture time scale of the s-process, estimated from s-process krypton in a meteorite

    NASA Technical Reports Server (NTRS)

    Matsuda, J.-I.; Lewis, R. S.; Anders, E.

    1980-01-01

    A krypton fraction enriched in s-process isotopes was extracted from a mineral fraction of the Murchison C2 chondrite. The (Kr-86)/(Kr-84) ratio is enhanced by 6 standard deviations, showing that significant amounts of Kr-86 were made in the s-process, despite the short, 10.8 yr beta-decay half-life of its precursor, Kr-85. Judging from this sample, the mean neutron capture time in the s-process was on the order of 5-100 yr for nuclei with cross sections of 125 mb.

  4. Debates—Perspectives on socio-hydrology: Capturing feedbacks between physical and social processes

    NASA Astrophysics Data System (ADS)

    Di Baldassarre, Giuliano; Viglione, Alberto; Carr, Gemma; Kuil, Linda; Yan, Kun; Brandimarte, Luigia; Blöschl, Günter

    2015-06-01

    In flood risk assessment, there remains a lack of analytical frameworks capturing the dynamics emerging from two-way feedbacks between physical and social processes, such as adaptation and levee effect. The former, "adaptation effect", relates to the observation that the occurrence of more frequent flooding is often associated with decreasing vulnerability. The latter, "levee effect", relates to the observation that the non-occurrence of frequent flooding (possibly caused by flood protection structures, e.g. levees) is often associated to increasing vulnerability. As current analytical frameworks do not capture these dynamics, projections of future flood risk are not realistic. In this paper, we develop a new approach whereby the mutual interactions and continuous feedbacks between floods and societies are explicitly accounted for. Moreover, we show an application of this approach by using a socio-hydrological model to simulate the behavior of two main prototypes of societies: green societies, which cope with flooding by resettling out of flood-prone areas; and technological societies, which deal with flooding also by building levees or dikes. This application shows that the proposed approach is able to capture and explain the aforementioned dynamics (i.e. adaptation and levee effect) and therefore contribute to a better understanding of changes in flood risk, within an iterative process of theory development and empirical research.

  5. Process analysis of CO{sub 2} capture from flue gas using carbonation/calcination cycles

    SciTech Connect

    Li, Z.S.; Cai, N.S.; Croiset, E.

    2008-07-15

    Process analysis of CO{sub 2} capture from flue gas using Ca-based carbonation/calcination cycles is presented here. A carbonation/calcination system is composed essentially of two reactors (an absorber and a regenerator) with Ca-based sorbent circulating between the two reactors (assumed here as fluidized beds). CO{sub 2} is, therefore, transferred from the absorber to the regenerator. Because of the endothermicity of the calcination reaction, a certain amount of coal is burned with pure oxygen in the regenerator. Detailed mass balance, heat balance and cost of electricity and CO{sub 2} mitigation for the carbonation/calcination cycles with three Ca-based sorbents in dual fluidized beds were calculated and analyzed to study the effect of the Ca-based sorbent activity decay on CO{sub 2} capture from flue gas. The three sorbents considered were: limestone, dolomite and CaO/Ca{sub 12}Al{sub 14}O{sub 33} (75/25 wt %) sorbent. All results, including the amount of coal and oxygen required, are presented with respect to the difference in calcium oxide conversion between the absorber and the regenerator, which is an important design parameter. Finally, costs of electricity and CO{sub 2} mitigation costs using carbonation/calcination cycles for the three sorbents were estimated. The results indicate that the economics of the carbonation/calcination process compare favorably with competing technologies for capturing CO{sub 2}.

  6. A design of real time image capturing and processing system using Texas Instrument's processor

    NASA Astrophysics Data System (ADS)

    Wee, Toon-Joo; Chaisorn, Lekha; Rahardja, Susanto; Gan, Woon-Seng

    2007-09-01

    In this work, we developed and implemented an image capturing and processing system that equipped with capability of capturing images from an input video in real time. The input video can be a video from a PC, video camcorder or DVD player. We developed two modes of operation in the system. In the first mode, an input image from the PC is processed on the processing board (development platform with a digital signal processor) and is displayed on the PC. In the second mode, current captured image from the video camcorder (or from DVD player) is processed on the board but is displayed on the LCD monitor. The major difference between our system and other existing conventional systems is that image-processing functions are performed on the board instead of the PC (so that the functions can be used for further developments on the board). The user can control the operations of the board through the Graphic User Interface (GUI) provided on the PC. In order to have a smooth image data transfer between the PC and the board, we employed Real Time Data Transfer (RTDX TM) technology to create a link between them. For image processing functions, we developed three main groups of function: (1) Point Processing; (2) Filtering and; (3) 'Others'. Point Processing includes rotation, negation and mirroring. Filter category provides median, adaptive, smooth and sharpen filtering in the time domain. In 'Others' category, auto-contrast adjustment, edge detection, segmentation and sepia color are provided, these functions either add effect on the image or enhance the image. We have developed and implemented our system using C/C# programming language on TMS320DM642 (or DM642) board from Texas Instruments (TI). The system was showcased in College of Engineering (CoE) exhibition 2006 at Nanyang Technological University (NTU) and have more than 40 users tried our system. It is demonstrated that our system is adequate for real time image capturing. Our system can be used or applied for

  7. Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

    SciTech Connect

    Vipperla, Ravikumar; Yee, Michael; Steele, Ray

    2012-11-01

    This report presents system and economic analysis for a carbon capture unit which uses an amino-silicone solvent for CO{sub 2} capture and sequestration (CCS) in a pulverized coal (PC) boiler. The amino-silicone solvent is based on GAP-1 with Tri-Ethylene Glycol (TEG) as a co-solvent. The report also shows results for a CCS unit based on a conventional approach using mono-ethanol amine (MEA). Models were developed for both processes and used to calculate mass and energy balances. Capital costs and energy penalty were calculated for both systems, as well as the increase in cost of electricity. The amino-silicone solvent based system demonstrates significant advantages compared to the MEA system.

  8. Carbon dioxide sequestration by direct mineral carbonation: process mineralogy of feed and products

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Rush, G.E.; Dahlin, Cheryl L.; Collins, W. Keith

    2001-01-01

    Direct mineral carbonation has been investigated as a process to convert gaseous CO2 into a geologically stable final form. The process utilizes a slurry of water, with bicarbonate and salt additions, mixed with a mineral reactant, such as olivine (Mg2SiO4) or serpentine [Mg3Si2O5(OH)4]. Carbon dioxide is dissolved into this slurry, resulting in dissolution of the mineral and precipitation of magnesium carbonate (MgCO3). Optimum results have been achieved using heat pretreated serpentine feed material and high partial pressure of CO2 (PCO2). Specific conditions include: 155?C; PCO2=185 atm; 15% solids. Under these conditions, 78% conversion of the silicate to the carbonate was achieved in 30 minutes. Process mineralogy has been utilized to characterize the feed and process products, and interpret the mineral dissolution and carbonate precipitation reaction paths.

  9. The WIMP Capture Process for Dark Stars in the Early Universe

    NASA Astrophysics Data System (ADS)

    Sivertsson, Sofia; Gondolo, Paolo

    2011-03-01

    The first stars to form in the universe may have been dark stars, powered by dark matter annihilation instead of nuclear fusion. The initial amount of dark matter gathered by the star gravitationally can sustain it only for a limited period of time. It has been suggested that capture of additional dark matter from the environment can prolong the dark star phase even to the present day. Here we show that this capture process is ineffective to prolong the life of the first generation of dark stars. We construct a Monte Carlo simulation that follows each weakly interacting massive particle (WIMP) in the dark matter halo as its orbit responds to the formation and evolution of the dark star, as it scatters off the star's nuclei, and as it annihilates inside the star. A rapid depletion of the WIMPs on orbits that cross the star causes the demise of the first generation of dark stars. We suggest that a second generation of dark stars may in principle survive much longer through capture. We comment on the effect of relaxing our assumptions.

  10. Development of a carbonate absorption-based process for post-combustion CO2 capture: The role of biocatalyst to promote CO2 absorption rate

    USGS Publications Warehouse

    Lu, Y.; Ye, X.; Zhang, Z.; Khodayari, A.; Djukadi, T.

    2011-01-01

    An Integrated Vacuum Carbonate Absorption Process (IVCAP) for post-combustion carbon dioxide (CO2) capture is described. IVCAP employs potassium carbonate (PC) as a solvent, uses waste or low quality steam from the power plant for CO2 stripping, and employs a biocatalyst, carbonic anhydrase (CA) enzyme, for promoting the CO2 absorption into PC solution. A series of experiments were performed to evaluate the activity of CA enzyme mixed in PC solutions in a stirred tank reactor system under various temperatures, CA dosages, CO2 loadings, CO2 partial pressures, and the presence of major flue gas contaminants. It was demonstrated that CA enzyme is an effective biocatalyst for CO2 absorption under IVCAP conditions. ?? 2011 Published by Elsevier Ltd.

  11. Utilization of the cyanobacteria Anabaena sp. CH1 in biological carbon dioxide mitigation processes.

    PubMed

    Chiang, Chang-Ling; Lee, Chi-Mei; Chen, Pei-Chung

    2011-05-01

    Before switching totally to alternative fuel stage, CO(2) mitigation process has considered a transitional strategy for combustion of fossil fuels inevitably. In comparison to other CO(2) mitigation options, such as oceanic or geologic injection, the biological photosynthetic process would present a far superior and sustainable solution under both environmental and social considerations. The utilization of the cyanobacteria Anabaena sp. CH1 in carbon dioxide mitigation processes is analyzed in our research. It was found that an original developed photobioreactor with internal light source exhibits high light utilization. Anabaena sp. CH1 demonstrates excellent CO(2) tolerance even at 15% CO(2) level. This enables flue gas from power plant to be directly introduced to Anabaena sp. CH1 culture. Double light intensity and increased 47% CO(2) bubble retention time could enhance CO(2) removal efficiencies by 79% and 67%, respectively. A maximum CO(2) fixation rate of 1.01 g CO(2)L(-1)day(-1) was measured experimentally.

  12. Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

    SciTech Connect

    Fresia, Megan; Vogt, Kirk

    2013-12-31

    GE Global Research is developing technology to remove carbon dioxide (CO{sub 2}) from the flue gas of coal-fired power plants. A mixture of 3-aminopropyl end-capped polydimethylsiloxane (GAP-1m) and triethylene glycol (TEG) is the preferred CO{sub 2} capture solvent. GE Global Research was contracted by the Department of Energy to test a bench-scale continuous CO{sub 2} absorption/desorption system using a GAP-1m/TEG mixture as the solvent. SiVance LLC was sub-contracted to provide the GAP-1m material and conduct an Environmental, Health, and Safety (EH&S) assessment for a 550 MW coal-fired power plant. Five components of the solvent, CAS#2469-55-8 (GAP-0), CAS#106214-84-0 (GAP-1-4), TEG, and methanol and xylene (minor contaminants from the aminosilicone) are included in this assessment. One by-product, GAP-1m/SOX salt, and dodecylbenzenesulfonic acid (DDBSA) were also identified for analysis. All of the solvent components and DDBSA are listed on the EPA’s TSCA Inventory allowing companies to manufacture and use the chemicals commercially. The toxicological effects of each component were defined, and control mechanisms necessary to comply with U.S. EH&S regulations are summarized. An engineering and control system, including environmental abatement, was described for minimizing exposure and release of the chemical components. Proper handling and storage recommendations are made for each chemical to minimize risk to workers and the surrounding community.

  13. Hybrid Membrane/Absorption Process for Post-combustion CO2 Capture

    SciTech Connect

    Li, Shiguang; Shou, S.; Pyrzynski, Travis; Makkuni, Ajay; Meyer, Howard

    2013-12-31

    This report summarizes scientific/technical progress made for bench-scale membrane contactor technology for post-combustion CO2 capture from DOE Contract No. DE-FE-0004787. Budget Period 1 (BP1) membrane absorber, Budget Period 2 (BP2) membrane desorber and Budget Period 3 (BP3) integrated system and field testing studies have been completed successfully and met or exceeded the technical targets (≥ 90% CO2 removal and CO2 purity of 97% in one membrane stage). Significant breakthroughs are summarized below: BP1 research: The feasibility of utilizing the poly (ether ether ketone), PEEK, based hollow fiber contractor (HFC) in combination with chemical solvents to separate and capture at least 90% of the CO2 from simulated flue gases has been successfully established. Excellent progress has been made as we have achieved the BP1 goal: ≥ 1,000 membrane intrinsic CO2 permeance, ≥ 90% CO2 removal in one stage, ≤ 2 psi gas side pressure drop, and ≥ 1 (sec)-1 mass transfer coefficient. Initial test results also show that the CO2 capture performance, using activated Methyl Diethanol Amine (aMDEA) solvent, was not affected by flue gas contaminants O2 (~3%), NO2 (66 ppmv), and SO2 (145 ppmv). BP2 research: The feasibility of utilizing the PEEK HFC for CO2-loaded solvent regeneration has been successfully established High CO2 stripping flux, one order of magnitude higher than CO2 absorption flux, have been achieved. Refined economic evaluation based on BP1 membrane absorber and BP2 membrane desorber laboratory test data indicate that the CO2 capture costs are 36% lower than DOE’s benchmark amine absorption technology. BP3 research: A bench-scale system utilizing a membrane absorber and desorber was integrated into a continuous CO2 capture process using contactors containing 10 to 20 ft2 of membrane area. The integrated process operation was stable through a 100-hour laboratory test, utilizing a simulated flue gas stream. Greater than 90% CO2 capture combined with 97

  14. Materials and processes for the effective capture and immobilization of radioiodine: A review

    NASA Astrophysics Data System (ADS)

    Riley, Brian J.; Vienna, John D.; Strachan, Denis M.; McCloy, John S.; Jerden, James L.

    2016-03-01

    The immobilization of radioiodine produced from reprocessing used nuclear fuel is a growing priority for research and development of nuclear waste forms. This review provides a comprehensive summary of the current issues surrounding processing and containment of 129I, the isotope of greatest concern due to its long half-life of 1.6 × 107 y and potential incorporation into the human body. Strategies for disposal of radioiodine, captured by both wet scrubbing and solid sorbents, are discussed, as well as potential iodine waste streams for insertion into an immobilization process. Next, consideration of direct disposal of salts, incorporation into glasses, ceramics, cements, and other phases is discussed. The bulk of the review is devoted to an assessment of various sorbents for iodine and of waste forms described in the literature, particularly inorganic minerals, ceramics, and glasses. This review also contains recommendations for future research needed to address radioiodine immobilization materials and processes.

  15. Enzyme inactivation in food processing using high pressure carbon dioxide technology.

    PubMed

    Hu, Wanfeng; Zhou, Linyan; Xu, Zhenzhen; Zhang, Yan; Liao, Xiaojun

    2013-01-01

    High pressure carbon dioxide (HPCD) is an effective non-thermal processing technique for inactivating deleterious enzymes in liquid and solid food systems. This processing method avoids high temperatures and exerts a minimal impact on the nutritional and sensory properties of foods, but extends shelf life by inhibiting or killing microorganisms and enzymes. Indigenous enzymes in food such as polyphenol oxidase (PPO), pectin methylesterase (PME), and lypoxygenase (LOX) may cause undesirable chemical changes in food attributes, showing the loss in color, texture, and flavor. For more than two decades, HPCD has proved its effectiveness in inactivating these enzymes. The HPCD-induced inactivation of some microbial enzymes responsible for microbial metabolism is also included. This review presents a survey of the published knowledge regarding the use of HPCD for the inactivation of these enzymes, and analyzes the factors controlling the efficiency of HPCD and speculates on the underlying mechanism that leads to enzyme inactivation.

  16. Nanostructured Graphene-Titanium Dioxide Composites Synthesized by a Single-Step Aerosol Process for Photoreduction of Carbon Dioxide

    PubMed Central

    Wang, Wei-Ning; Jiang, Yi; Fortner, John D.; Biswas, Pratim

    2014-01-01

    Abstract Photocatalytic reduction of carbon dioxide (CO2) to hydrocarbons by using nanostructured materials activated by solar energy is a promising approach to recycling CO2 as a fuel feedstock. CO2 photoreduction, however, suffers from low efficiency mainly due to the inherent drawback of fast electron-hole recombination in photocatalysts. This work reports the synthesis of nanostructured composites of titania (TiO2) nanoparticles (NPs) encapsulated by reduced graphene oxide (rGO) nanosheets via an aerosol approach. The role of synthesis temperature and TiO2/GO ratio in CO2 photoreduction was investigated. As-prepared nanocomposites demonstrated enhanced CO2 conversion performance as compared with that of pristine TiO2 NPs due to the strong electron trapping capability of the rGO nanosheets. PMID:25053879

  17. Study of process variables in supercritical carbon dioxide extraction of soybeans.

    PubMed

    Wilkinson, Nikolas; Hilton, Ramsey; Hendry, Doug; Venkitasamy, Chandrasekar; Jacoby, William

    2014-01-01

    Soybean flakes were extracted using supercritical carbon dioxide at 48.3 MPa and 80 °C, which is a higher temperature than previously reported. Several operational parameters were explored to determine their effect on extractions. Flakes, as typically used in this industry, provided the best extraction performance. Particle size distributions were created through grinding. Reducing average particle diameters smaller than 0.069 mm had no appreciable effect on increasing extraction efficiencies. Exploration of flow rate indicated that a residence time of less than 60 s for the supercritical carbon dioxide would be sufficient for complete extractions. A solvent mass to load mass ratio of 10:1 was found to be sufficient for extraction of oils from soybean flakes. Increasing moisture in the soybeans led to decreasing extraction efficiency of oils. Finally, soybean hulls had no effect on extraction efficiency. Thus, the de-hulling procedure can be removed from the extraction process without decreasing extraction efficiency.

  18. Thermal and energetic processing of ammonia and carbon dioxide bearing solid mixtures.

    PubMed

    Lv, X Y; Boduch, P; Ding, J J; Domaracka, A; Langlinay, T; Palumbo, M E; Rothard, H; Strazzulla, G

    2014-02-28

    We present new experimental results on thermal and ion irradiation processing of frozen ammonia-carbon dioxide mixtures. Some mixtures were deposited at low temperatures (T ≈ 16 K). Upon warming up to 160 K, complex chemical reactions occur leading to the formation of new molecules and, in particular, of ammonium carbamate. We also show that the same species are produced when water is the dominant species in the ternary mixture with ammonia and carbon dioxide. The samples have been irradiated with 144 keV S(9+) ions at 16 K and 50 K. Also in this case, new chemical species are formed as e.g. ammonium formate, CO and OCN(-). The results are discussed in the light of their relevance to the chemical evolution of ices in the interstellar medium and in the solar system. In particular, we suggest searching for them among the gas phase species sublimating from grains around young stellar objects and from the cometary nuclei approaching the Sun. PMID:24358469

  19. Preparation and characterization of Polyacrylonitrile/ Manganese Dioxides- based Carbon Nanofibers via electrospinning process

    NASA Astrophysics Data System (ADS)

    Che Othman, F. E.; Yusof, N.; Jaafar, J.; Ismail, A. F.; Hasbullah, H.; Abdullah, N.; Ismail, M. S.

    2016-06-01

    This research reports the production of precursor polyacrylonitrile (PAN)/ manganese dioxide (MnO2) nanofibers (NFs) via electrospinning method followed by stabilization and carbonization processes. Nowadays, electrospinning has become a suitable method in manufacturing continuous NFs, thus it is employed to fabricate NFs in this study. The microstructural properties and adsorption competencies of the produced NFs were also studied. The NFs were prepared by electrospinning the polymer solution of Polyacrylonitrile (PAN) and Manganese Dioxide (MnO2) in, N, N-Dimethylformamide (DMF) solvent. The factors considered in this study were various polymer PAN/MnO2 concentrations which will significantly affect the specific surface area, fiber morphology and the diameter of the NFs prepared. Subsequently, heat treatment is applied by setting up the stabilization temperature at 275 °C and carbonization temperature at 800 °C with constant dwelling time (30 min). Nitrogen gas at constant rate 0.2 L/min was used for stabilization and carbonization with the stabilization rate (2 °C/min) and carbonization rate (5 °C/min). The carbon nanofibers (CNFs) produced were characterized using Scanning Electron Microscopy (SEM), Brunauer Emmett and Teller (BET) surface area and Fourier Transmission Infrared Spectroscopy (FTIR). It was found that the PAN/MnO2 CNFs were successfully produced with the carbonization temperature of 800 °C. The prepared PAN/MnO2 CNFs prepared showed an enhanced in specific surface area about two times compared to it precursor NFs.

  20. Modelling the impacts of climate policy on the deployment of carbon dioxide capture and geologic storage across electric power regions in the United States

    SciTech Connect

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

    2007-04-02

    This paper summarizes the results of a first-of-its-kind holistic, integrated economic analysis of the potential role of carbon dioxide (CO2) capture and storage (CCS) technologies across the regional segments of the United States of America (USA) electric power sector, over the time frame 2005-2045, in response to two hypothetical emissions control policies analyzed against two potential energy supply futures that include updated and substantially higher projected prices for natural gas. A key feature of this paper’s analysis is an attempt to explicitly model the inherent heterogeneities that exist in both the nation’s current and future electricity generation infrastructure and candidate deep geologic CO2 storage formations. Overall, between 180 and 580 gigawatts (GW) of coal-fired integrated gasification combined cycle with CCS (IGCC+CCS) capacity is built by 2045 in these four scenarios, requiring between 12 and 41gigatons of CO2 (GtCO2) of storage in regional deep geologic reservoirs across the USA. Nearly all of this CO2 is from new IGCC+CCS systems, which start to deploy after 2025. Relatively little IGCC+CCS capacity is built before that time, primarily under unique niche opportunities. For the most part, CO2 emissions prices will likely need to be sustained at well over $10-20/ton CO2 before CCS begins to deploy on a large scale within the electric power sector. Within these broad national trends, a highly nuanced picture of CCS deployment across the USA emerges. Across the four scenarios studied here, some North American Electric Reliability Council (NERC) regions do not employ any CCS while others build more than 100 GW of CCS-enabled generation capacity. One region sees as much as 50% of their geologic CO2 storage reservoirs’ total theoretical capacity consumed by 2045, while the majority of the regions still have more than 90% of their potential storage capacity available to meet storage needs in the second half of the century and beyond.

  1. The Ansel Adams zone system: HDR capture and range compression by chemical processing

    NASA Astrophysics Data System (ADS)

    McCann, John J.

    2010-02-01

    We tend to think of digital imaging and the tools of PhotoshopTM as a new phenomenon in imaging. We are also familiar with multiple-exposure HDR techniques intended to capture a wider range of scene information, than conventional film photography. We know about tone-scale adjustments to make better pictures. We tend to think of everyday, consumer, silver-halide photography as a fixed window of scene capture with a limited, standard range of response. This description of photography is certainly true, between 1950 and 2000, for instant films and negatives processed at the drugstore. These systems had fixed dynamic range and fixed tone-scale response to light. All pixels in the film have the same response to light, so the same light exposure from different pixels was rendered as the same film density. Ansel Adams, along with Fred Archer, formulated the Zone System, staring in 1940. It was earlier than the trillions of consumer photos in the second half of the 20th century, yet it was much more sophisticated than today's digital techniques. This talk will describe the chemical mechanisms of the zone system in the parlance of digital image processing. It will describe the Zone System's chemical techniques for image synthesis. It also discusses dodging and burning techniques to fit the HDR scene into the LDR print. Although current HDR imaging shares some of the Zone System's achievements, it usually does not achieve all of them.

  2. Optimization of water use and cost of electricity for an MEA carbon capture process, January 26, 2012

    SciTech Connect

    Eslick, J.; Miller, D.

    2012-01-01

    DOE goals are: 90% CO{sub 2} capture, Less than 30% increase in COE, and to reduce water use by 70% at 50% cost of dry cooling. Objectives are: (1) Develop detailed models of supercritical power plant, MEA carbon capture process, CO{sub 2} compression; and (2) Optimize process for conflicting goals of minimizing water use and COE CO{sub 2} capture greatly increases COE and water use, power gen. 1/3 of fresh water use, and water scarcity is increasing.

  3. Advancing adsorption and membrane separation processes for the gigaton carbon capture challenge.

    PubMed

    Wilcox, Jennifer; Haghpanah, Reza; Rupp, Erik C; He, Jiajun; Lee, Kyoungjin

    2014-01-01

    Reducing CO2 in the atmosphere and preventing its release from point-source emitters, such as coal and natural gas-fired power plants, is a global challenge measured in gigatons. Capturing CO2 at this scale will require a portfolio of gas-separation technologies to be applied over a range of applications in which the gas mixtures and operating conditions will vary. Chemical scrubbing using absorption is the current state-of-the-art technology. Considerably less attention has been given to other gas-separation technologies, including adsorption and membranes. It will take a range of creative solutions to reduce CO2 at scale, thereby slowing global warming and minimizing its potential negative environmental impacts. This review focuses on the current challenges of adsorption and membrane-separation processes. Technological advancement of these processes will lead to reduced cost, which will enable subsequent adoption for practical scaled-up application. PMID:24702296

  4. Advancing adsorption and membrane separation processes for the gigaton carbon capture challenge.

    PubMed

    Wilcox, Jennifer; Haghpanah, Reza; Rupp, Erik C; He, Jiajun; Lee, Kyoungjin

    2014-01-01

    Reducing CO2 in the atmosphere and preventing its release from point-source emitters, such as coal and natural gas-fired power plants, is a global challenge measured in gigatons. Capturing CO2 at this scale will require a portfolio of gas-separation technologies to be applied over a range of applications in which the gas mixtures and operating conditions will vary. Chemical scrubbing using absorption is the current state-of-the-art technology. Considerably less attention has been given to other gas-separation technologies, including adsorption and membranes. It will take a range of creative solutions to reduce CO2 at scale, thereby slowing global warming and minimizing its potential negative environmental impacts. This review focuses on the current challenges of adsorption and membrane-separation processes. Technological advancement of these processes will lead to reduced cost, which will enable subsequent adoption for practical scaled-up application.

  5. Subaru/HDS study of CH stars: elemental abundances for stellar neutron-capture process studies

    NASA Astrophysics Data System (ADS)

    Goswami, Aruna; Aoki, Wako; Karinkuzhi, Drisya

    2016-01-01

    A comprehensive abundance analysis providing rare insight into the chemical history of lead stars is still lacking. We present results from high-resolution (R ˜ 50 000) spectral analyses of three CH stars, HD 26, HD 198269 and HD 224959, and, a carbon star with a dusty envelope, HD 100764. Previous studies on these objects are limited by both resolution and wavelength regions and the results differ significantly from each other. We have undertaken to reanalyse the chemical composition of these objects based on high-resolution Subaru spectra covering the wavelength regions 4020-6775 Å. Considering local thermodynamic equilibrium and using model atmospheres, we have derived the stellar parameters, the effective temperatures Teff, surface gravities log g, and metallicities [Fe/H] for these objects. The derived parameters for HD 26, HD 100764, HD 198269 and HD 224959 are (5000, 1.6, -1.13), (4750, 2.0 -0.86), (4500, 1.5, -2.06) and (5050, 2.1, -2.44), respectively. The stars are found to exhibit large enhancements of heavy elements relative to iron in conformity to previous studies. Large enhancement of Pb with respect to iron is also confirmed. Updates on the elemental abundances for several s-process elements (Y, Zr, La, Ce, Nd, Sm and Pb) along with the first-time estimates of abundances for a number of other heavy elements (Sr, Ba, Pr, Eu, Er and W) are reported. Our analysis suggests that neutron-capture elements in HD 26 primarily originate in the s-process while the major contributions to the abundances of neutron-capture elements in the more metal-poor objects HD 224959 and HD 198269 are from the r-process, possibly from materials that are pre-enriched with products of the r-process.

  6. Multi-layer VEB modeling: capturing interlayer etch process effects for multi-patterning process

    NASA Astrophysics Data System (ADS)

    Hu, Lin; Jung, Sunwook; Li, Jianliang; Kim, Young; Bar, Yuval; Lobb, Granger; Liang, Jim; Ogino, Atsushi; Sturtevant, John; Bailey, Todd

    2016-03-01

    Self-Aligned Via (SAV) process is commonly used in back end of line (BEOL) patterning. As the technology node advances, tightening CD and overlay specs require continuous improvement in model accuracy of the SAV process. Traditional single layer Variable Etch Bias (VEB) model is capable of describing the micro-loading and aperture effects associated with the reactive ion etch (RIE), but it does not include effects from under layers. For the SAV etch, a multi-layer VEB model is needed to account for the etch restriction from metal trenches. In this study, we characterize via post-etch dimensions through pitch and through metal trench widths, and show that VEB model prediction accuracy for SAV CDs after SAV formation can be significantly improved by applying a multi-layer scheme. Using a multi-layer VEB, it is demonstrated that the output via size changes with varying trench dimensions, which matches the silicon results. The model also reports via shape post-etch as a function of trench environment, where elliptical vias are correctly produced. The multi-layer VEB model can be applied both multi-layer correction and verification in full chip flow. This paper will also suggest that the multi-layer VEB model can be used in other FEOL layers with interlayer etch process effects, such as gate cut, to support the robustness of new model.

  7. Production of small uranium dioxide microspheres for cermet nuclear fuel using the internal gelation process

    SciTech Connect

    Collins, Robert T; Collins, Jack Lee; Hunt, Rodney Dale; Ladd-Lively, Jennifer L; Patton, Kaara K; Hickman, Robert

    2014-01-01

    The U.S. National Aeronautics and Space Administration (NASA) is developing a uranium dioxide (UO2)/tungsten cermet fuel for potential use as the nuclear cryogenic propulsion stage (NCPS). The first generation NCPS is expected to be made from dense UO2 microspheres with diameters between 75 and 150 m. Previously, the internal gelation process and a hood-scale apparatus with a vibrating nozzle were used to form gel spheres, which became UO2 kernels with diameters between 350 and 850 m. For the NASA spheres, the vibrating nozzle was replaced with a custom designed, two-fluid nozzle to produce gel spheres in the desired smaller size range. This paper describes the operational methodology used to make 3 kg of uranium oxide microspheres.

  8. Separation processes for recovering alloy steels from grinding sludge: Supercritical carbon dioxide extraction and aqueous cleaning

    SciTech Connect

    Fu, H.; Matthews, M.A.

    1999-04-01

    Two separation processes have been developed to remove contaminants (cutting oil with trace phosphorus additive) from high-speed steel grinding sludge. One process uses an aqueous surfactant washing technique, and the second process uses supercritical carbon dioxide (SCCO{sub 2}) extraction. Bench-scale aqueous washings have shown that the required phosphorus removal is easily obtained, but a sufficient oil removal is more difficult. The experimental results also indicate a strong dependence of the aqueous washing efficiency on the choice of a suitable surfactant. A mass transfer model is used to simulate a semi-continuous washing process. SCCO{sub 2} extraction at 80 C and 340 atm shows that approximately 80% of the oil can be removed from the sludge during a 60-minute process to produce a batch of recyclable steel, and that the phosphorus removal also reaches the required level. A linear desorption model is used to describe the irreversible desorption of oil from the solid phase into the CO{sub 2} phase, and the simulated results agree very well with the experimental data.

  9. Cribellate thread production in spiders: Complex processing of nano-fibres into a functional capture thread.

    PubMed

    Joel, Anna-Christin; Kappel, Peter; Adamova, Hana; Baumgartner, Werner; Scholz, Ingo

    2015-11-01

    Spider silk production has been studied intensively in the last years. However, capture threads of cribellate spiders employ an until now often unnoticed alternative of thread production. This thread in general is highly interesting, as it not only involves a controlled arrangement of three types of threads with one being nano-scale fibres (cribellate fibres), but also a special comb-like structure on the metatarsus of the fourth leg (calamistrum) for its production. We found the cribellate fibres organized as a mat, enclosing two parallel larger fibres (axial fibres) and forming the typical puffy structure of cribellate threads. Mat and axial fibres are punctiform connected to each other between two puffs, presumably by the action of the median spinnerets. However, this connection alone does not lead to the typical puffy shape of a cribellate thread. Removing the calamistrum, we found a functional capture thread still being produced, but the puffy shape of the thread was lost. Therefore, the calamistrum is not necessary for the extraction or combination of fibres, but for further processing of the nano-scale cribellate fibres. Using data from Uloborus plumipes we were able to develop a model of the cribellate thread production, probably universally valid for cribellate spiders.

  10. Use of chlorine dioxide in a secondary recovery process to inhibit bacterial fouling and corrosion

    SciTech Connect

    Knickrehm, M.; Caballero, E.; Romualdo, P.; Sandidge, J.

    1987-01-01

    A major oil company operates a secondary recovery waterflood in Inglewood, California. The waterflood currently processes 250,000 bbls. per day of produced fluid. The major economic and operational problems associated with a secondary recovery waterflood are: 1) corrosion due to oxygen, carbon dioxide, hydrogen sulfide, and bacteria (sulfate reducers and slime biomass), 2) plugging from deposits due to salts, sulfides, and biofilms. These problems lead to deterioration of water handling equipment, injection lines (surface and subsurface), and decreased water quality resulting in the plugging of injection wells. During the last 8 years the operator has used varying mechanical and chemical technology to solve these problems. From 1978 to 1982 traditional chemical programs were in effect. Over this time period there was a continuing decline in water quality, and a substantial increase in chemical and operational costs. It was determined at that time that the major reason for this was due to microbiological activity. With this in mind, the operator proceeded to test the effects of using Aqueous Chlorine Dioxide in one portion of their water handling facilities. Due to the success of the program it was applied field wide. Presently, the primary problems associated with bacteria have been arrested. Solving one corrosion problem can lead to the onset of another. The operator is now in the process of making a concentrated effort to eliminate the other synergistically related corrosive and plugging agents (O/sub 2/, CO/sub 2/, H/sub 2/S). A field history of the problems, findings, and solutions, are discussed along with an overview of our present direction.

  11. Colorimetric detection of hazardous gases using a remotely operated capturing and processing system.

    PubMed

    Montes-Robles, Roberto; Moragues, María Esperanza; Vivancos, José-Luis; Ibáñez, Javier; Fraile, Rubén; Martínez-Máñez, Ramón; García-Breijo, Eduardo

    2015-11-01

    This paper presents an electronic system for the automatic detection of hazardous gases. The proposed system implements colorimetric sensing algorithms, thus providing a low-cost solution to the problem of gas sensing. It is remotely operated and it performs the tasks of image capturing and processing, hence obtaining colour measurements in RGB (Red-Green-Blue) space that are subsequently sent to a remote operator via the internet. A prototype of the system has been built to test its performance. Specifically, experiments have been carried out aimed at the detection of CO, CO2, NO, NO2, SO2 and formaldehyde at diverse concentrations by using a chromogenic array composed by 13 active and 2 inert compounds. Statistical analyses of the results reveal a good performance of the electronic system and the feasibility of remote hazardous gas detection using colorimetric sensor arrays.

  12. Failure of the multiple peaking approximation for fast capture processes at milliradian scattering angles

    SciTech Connect

    Houamer, Salim; Popov, Yuri V.; Dal Cappello, Claude

    2010-03-15

    The first Born approximation is examined for different fast capture processes for the p+He system at incident energies of about 1 MeV. Calculations have been performed for the singly differential cross section (SDCS) for scattering angles 0-0.5 mrad in the laboratory frame. In the case of transfer ionization, we observe that the two-step-2 mechanism has a dominant contribution to the SDCS for the kinematics considered in this work. The present investigation demonstrates that the multiple peaking approximation is a very crude method which fails to describe the SDCS even at scattering angles below 0.5 mrad. We have also presented a doubly differential cross section for the fixed emission energy of 600 eV and compared our results with other theoretical calculations and experiments.

  13. Colorimetric detection of hazardous gases using a remotely operated capturing and processing system.

    PubMed

    Montes-Robles, Roberto; Moragues, María Esperanza; Vivancos, José-Luis; Ibáñez, Javier; Fraile, Rubén; Martínez-Máñez, Ramón; García-Breijo, Eduardo

    2015-11-01

    This paper presents an electronic system for the automatic detection of hazardous gases. The proposed system implements colorimetric sensing algorithms, thus providing a low-cost solution to the problem of gas sensing. It is remotely operated and it performs the tasks of image capturing and processing, hence obtaining colour measurements in RGB (Red-Green-Blue) space that are subsequently sent to a remote operator via the internet. A prototype of the system has been built to test its performance. Specifically, experiments have been carried out aimed at the detection of CO, CO2, NO, NO2, SO2 and formaldehyde at diverse concentrations by using a chromogenic array composed by 13 active and 2 inert compounds. Statistical analyses of the results reveal a good performance of the electronic system and the feasibility of remote hazardous gas detection using colorimetric sensor arrays. PMID:26434416

  14. Understanding volcanic processes using UV camera measurements of sulfur dioxide and coincident infrasound and seismicity

    NASA Astrophysics Data System (ADS)

    Dalton, Marika Piirak

    The exsolution of volatiles from magma maintains an important control on volcanic eruption styles. The nucleation, growth, and connectivity of bubbles during magma ascent provide the driving force behind eruptions, and the rate, volume, and ease of gas exsolution can affect eruptive activity. Volcanic plumes are the observable consequence of this magmatic degassing, and remote sensing techniques allow us to quantify changes in gas exsolution. However, until recently the methods used to measure volcanic plumes did not have the capability of detecting rapid changes in degassing on the scale of standard geophysical observations. The advent of the UV camera now makes high sample rate gas measurements possible. This type of dataset can then be compared to other volcanic observations to provide an in depth picture of degassing mechanisms in the shallow conduit. The goals of this research are to develop a robust methodology for UV camera field measurements of volcanic plumes, and utilize this data in conjunction with seismoacoustic records to illuminate degassing processes. Field and laboratory experiments were conducted to determine the effects of imaging conditions, vignetting, exposure time, calibration technique, and filter usage on the UV camera sulfur dioxide measurements. Using the best practices determined from these studies, a field campaign was undertaken at Volcan de Pacaya, Guatemala. Coincident plume sulfur dioxide measurements, acoustic recordings, and seismic observations were collected and analyzed jointly. The results provide insight into the small explosive features, variations in degassing rate, and plumbing system of this complex volcanic system. This research provides useful information for determining volcanic hazard at Pacaya, and demonstrates the potential of the UV camera in multiparameter studies.

  15. Process modeling of an advanced NH₃ abatement and recycling technology in the ammonia-based CO₂ capture process.

    PubMed

    Li, Kangkang; Yu, Hai; Tade, Moses; Feron, Paul; Yu, Jingwen; Wang, Shujuan

    2014-06-17

    An advanced NH3 abatement and recycling process that makes great use of the waste heat in flue gas was proposed to solve the problems of ammonia slip, NH3 makeup, and flue gas cooling in the ammonia-based CO2 capture process. The rigorous rate-based model, RateFrac in Aspen Plus, was thermodynamically and kinetically validated by experimental data from open literature and CSIRO pilot trials at Munmorah Power Station, Australia, respectively. After a thorough sensitivity analysis and process improvement, the NH3 recycling efficiency reached as high as 99.87%, and the NH3 exhaust concentration was only 15.4 ppmv. Most importantly, the energy consumption of the NH3 abatement and recycling system was only 59.34 kJ/kg CO2 of electricity. The evaluation of mass balance and temperature steady shows that this NH3 recovery process was technically effective and feasible. This process therefore is a promising prospect toward industrial application.

  16. Ab initio Calculation of the np→dγ Radiative Capture Process.

    PubMed

    Beane, Silas R; Chang, Emmanuel; Detmold, William; Orginos, Kostas; Parreño, Assumpta; Savage, Martin J; Tiburzi, Brian C

    2015-09-25

    Lattice QCD calculations of two-nucleon systems are used to isolate the short-distance two-body electromagnetic contributions to the radiative capture process np→dγ, and the photo-disintegration processes γ^{(*)}d→np. In nuclear potential models, such contributions are described by phenomenological meson-exchange currents, while in the present work, they are determined directly from the quark and gluon interactions of QCD. Calculations of neutron-proton energy levels in multiple background magnetic fields are performed at two values of the quark masses, corresponding to pion masses of m_{π}~450 and 806 MeV, and are combined with pionless nuclear effective field theory to determine the amplitudes for these low-energy inelastic processes. At m_{π}~806 MeV, using only lattice QCD inputs, a cross section σ^{806 MeV}~17 mb is found at an incident neutron speed of v=2,200 m/s. Extrapolating the short-distance contribution to the physical pion mass and combining the result with phenomenological scattering information and one-body couplings, a cross section of σ^{lqcd}(np→dγ)=334.9(+5.2-5.4) mb is obtained at the same incident neutron speed, consistent with the experimental value of σ^{expt}(np→dγ)=334.2(0.5) mb. PMID:26451545

  17. Process for CO.sub.2 capture using a regenerable magnesium hydroxide sorbent

    DOEpatents

    Siriwardane, Ranjani V; Stevens, Jr., Robert W

    2013-06-25

    A process for CO.sub.2 separation using a regenerable Mg(OH).sub.2 sorbent. The process absorbs CO.sub.2 through the formation of MgCO.sub.3 and releases water product H.sub.2O. The MgCO.sub.3 is partially regenerated through direct contact with steam, which acts to heat the magnesium carbonate to a higher temperature, provide heat duty required to decompose the magnesium carbonate to yield MgO and CO.sub.2, provide an H.sub.2O environment over the magnesium carbonate thereby shifting the equilibrium and increasing the potential for CO.sub.2 desorption, and supply H.sub.2O for rehydroxylation of a portion of the MgO. The mixture is polished in the absence of CO.sub.2 using water product H.sub.2O produced during the CO.sub.2 absorption to maintain sorbent capture capacity. The sorbent now comprised substantially of Mg(OH).sub.2 is then available for further CO.sub.2 absorption duty in a cyclic process.

  18. Integrated Electrochemical Processes for CO2 Capture and Conversion to Commodity Chemicals

    SciTech Connect

    Hatton, T. Alan; Jamison, Timothy

    2013-09-30

    The Massachusetts Institute of Technology (MIT) and Siemens Corporations (SCR) are developing new chemical synthesis processes for commodity chemicals from CO2. The process is assessed as a novel chemical sequestration technology that utilizes CO2 from dilute gas streams generated at industrial carbon emitters as a raw material to produce useful commodity chemicals. Work at Massachusetts Institute of Technology (MIT) commenced on October 1st, 2010, and finished on September 30th, 2013. During this period, we have investigated and accomplished five objectives that mainly focused on converting CO2 into high-value chemicals: 1) Electrochemical assessment of catalytic transformation of CO2 and epoxides to cyclic carbonates; 2) Investigation of organocatalytic routes to convert CO2 and epoxide to cyclic carbonates; 3) Investigation of CO2 Capture and conversion using simple olefins under continuous flow; 4) Microwave assisted synthesis of cyclic carbonates from olefins using sodium bicarbonates in a green pathway; 5) Life cycle analyses of integrated chemical sequestration process. In this final report, we will describe the detailed study performed during the three year period and findings and conclusions drawn from our research.

  19. Ab initio calculation of the $np \\to d ³$ radiative capture process

    SciTech Connect

    Beane, Silas R.; Chang, Emmanuel; Detmold, William; Orginos, Kostas; Parreño, Assumpta; Savage, Martin J.; Tiburzi, Brian C.

    2015-09-24

    In this study, lattice QCD calculations of two-nucleon systems are used to isolate the short-distance two-body electromagnetic contributions to the radiative capture process $np \\to d\\gamma$, and the photo-disintegration processes $\\gamma^{(\\ast)} d \\to np$. In nuclear potential models, such contributions are described by phenomenological meson-exchange currents, while in the present work, they are determined directly from the quark and gluon interactions of QCD. Calculations of neutron-proton energy levels in multiple background magnetic fields are performed at two values of the quark masses, corresponding to pion masses of $m_\\pi \\sim 450$ and 806 MeV, and are combined with pionless nuclear effective field theory to determine these low-energy inelastic processes. Extrapolating to the physical pion mass, a cross section of $\\sigma^{lqcd}(np\\to d\\gamma)=332.4({\\tiny \\begin{array}{l}+5.4 \\\\ - 4.7\\end{array}})\\ mb$ is obtained at an incident neutron speed of $v=2,200\\ m/s$, consistent with the experimental value of $\\sigma^{expt}(np \\to d\\gamma) = 334.2(0.5)\\ mb$.

  20. COMPARISON OF SODIUM AND POTASSIUM CARBONATES AS LITHIUM ZIRCONATE MODIFIERS FOR HIGH-TEMPERATURE CARBON DIOXIDE CAPTURE FROM BIOMASS-DERIVED SYNTHESIS GAS

    SciTech Connect

    Olstad, J.L.; Phillips, S.D.

    2009-01-01

    The process of gasifi cation converts biomass into synthesis gas (syngas), which can be used to produce biofuels. Solid-phase sorbents were investigated for the removal of CO2 from a N2/CO2 gas stream using a CO2 concentration similar to that found in a biomass gasifi cation process. During the gasifying process, large amounts of carbon dioxide (CO2) are created along with the syngas. The produced CO2 must be removed before the syngas can be used for fuel synthesis and to avoid the possible formation of unwanted byproducts. A thermogravimetric analyzer was used to test the CO2 absorption rates of sorbents composed of lithium zirconate (Li2ZrO3), as well as mixtures of Li2ZrO3 with potassium carbonate (K2CO3) and sodium carbonate (Na2CO3). The experimental results show that Li2ZrO3 has a low absorption rate, but sorbents containing combinations of Li2ZrO3 and the K2CO3 and Na2CO3 additives have high uptake rates. Using different proportions of K2CO3 and Na2CO3 produces varying uptake rates, so an optimization experiment was performed to obtain an improved sorbent. The CO2 absorption and regeneration stability of the solid-phase sorbents were also examined. A sorbent composed of Li2ZrO3 and 12.1 weight % Na2CO3 was shown to be stable, based on the consistent CO2 uptake rates. Sorbents prepared with Li2ZrO3, 17.6 weight % K2CO3 and 18.1 weight % Na2CO3 showed instability during regeneration cycles in air at 800 °C. Sorbent stability improved during regeneration cycles at 700 °C. Further testing of the Li2ZrO3 sorbent under actual syngas conditions, including higher pressure and composition, should be done. Once the optimum sorbent has been found, a suitable support will be needed to use the sorbent in an actual reactor.

  1. Ab initio calculation of the $$np \\to d ³$$ radiative capture process

    DOE PAGESBeta

    Beane, Silas R.; Chang, Emmanuel; Detmold, William; Orginos, Kostas; Parreño, Assumpta; Savage, Martin J.; Tiburzi, Brian C.

    2015-09-24

    In this study, lattice QCD calculations of two-nucleon systems are used to isolate the short-distance two-body electromagnetic contributions to the radiative capture processmore » $$np \\to d\\gamma$$, and the photo-disintegration processes $$\\gamma^{(\\ast)} d \\to np$$. In nuclear potential models, such contributions are described by phenomenological meson-exchange currents, while in the present work, they are determined directly from the quark and gluon interactions of QCD. Calculations of neutron-proton energy levels in multiple background magnetic fields are performed at two values of the quark masses, corresponding to pion masses of $$m_\\pi \\sim 450$$ and 806 MeV, and are combined with pionless nuclear effective field theory to determine these low-energy inelastic processes. Extrapolating to the physical pion mass, a cross section of $$\\sigma^{lqcd}(np\\to d\\gamma)=332.4({\\tiny \\begin{array}{l}+5.4 \\\\ - 4.7\\end{array}})\\ mb$$ is obtained at an incident neutron speed of $$v=2,200\\ m/s$$, consistent with the experimental value of $$\\sigma^{expt}(np \\to d\\gamma) = 334.2(0.5)\\ mb$$.« less

  2. ADVANCED OXYFUEL BOILERS AND PROCESS HEATERS FOR COST EFFECTIVE CO2 CAPTURE AND SEQUESTRATION

    SciTech Connect

    John Sirman; Leonard Switzer; Bart van Hassel

    2004-06-01

    This annual technical progress report summarizes the work accomplished during the second year of the program, January-December 2003, in the following task areas: Task 1--Conceptual Design, Task 2--Laboratory Scale Evaluations, Task 3--OTM Development, Task 4--Economic Evaluation and Commercialization Planning and Task 5--Program Management. The program has experienced significant delays due to several factors. The budget has also been significantly under spent. Based on recent technical successes and confirmation of process economics, significant future progress is expected. Concepts for integrating Oxygen Transport Membranes (OTMs) into boilers and process heaters to facilitate oxy-fuel combustion have been investigated. OTM reactor combustion testing was delayed to insufficient reliability of the earlier OTM materials. Substantial improvements to reliability have been identified and testing will recommence early in 2004. Promising OTM material compositions and OTM architectures have been identified that improve the reliability of the ceramic elements. Economic evaluation continued. Information was acquired that quantified the attractiveness of the advanced oxygen-fired boiler. CO{sub 2} capture and compression are still estimated to be much less than $10/ton CO{sub 2}.

  3. Using Visual Methods to Capture Embedded Processes of Resilience for Youth across Cultures and Contexts

    PubMed Central

    Didkowsky, Nora; Ungar, Michael; Liebenberg, Linda

    2010-01-01

    Objectives: We review the value of using visual data in a dialogue with youth, to reflect, explore and find language to better understand processes of resilience. Methods: The argument is demonstrated with examples from the Negotiating Resilience Project (NRP): an international study of 16 youth which uses video recording a day in the life of youth participants, photographs produced by youth, and reflective interviews with the youth about their visual data. Results: Three examples from the NRP are used to show the ways that visual methods can capture and elucidate previously hidden aspects of youth’s positive psychosocial development in stressful social ecologies. Conclusion: Incorporating images as research data can aid in understanding previously unarticulated constructions of youth resilience. When the researcher is reflexive about power dynamics and their role in co-constructing the research environment, visual methods have the potential to reduce power imbalances in the field, meaningfully engage youth in the research process, and help to overcome language barriers. PMID:20119562

  4. Galactic evolution of rapid neutron capture process abundances: the inhomogeneous approach

    NASA Astrophysics Data System (ADS)

    Wehmeyer, B.; Pignatari, M.; Thielemann, F.-K.

    2015-09-01

    For the origin of heavy rapid neutron capture process (r-process) elements, different sources have been proposed, e.g. core-collapse supernovae or neutron star mergers. Old metal-poor stars carry the signature of the astrophysical source(s). Among the elements dominantly made by the r-process, europium (Eu) is relatively easy to observe. In this work we simulate the evolution of Eu in our Galaxy with the inhomogeneous chemical evolution (ICE) model, and compare our results with spectroscopic observations. We test the most important parameters affecting the chemical evolution of Eu: (a) for neutron star mergers the coalescence time-scale of the merger (tcoal) and the probability to experience a neutron star merger event after two supernova explosions occurred and formed a double neutron star system (PNSM) and (b) for the subclass of magnetorotationally driven supernovae (`Jet-SNe'), their occurrence rate compared to standard supernovae (PJet-SN). We find that the observed [Eu/Fe] pattern in the Galaxy can be reproduced by a combination of neutron star mergers and Jet-SNe as r-process sources. While neutron star mergers alone seem to set in at too high metallicities, Jet-SNe provide a cure for this deficiency at low metallicities. Furthermore, we confirm that local inhomogeneities can explain the observed large spread in the Eu abundances at low metallicities. We also predict the evolution of [O/Fe] to test whether the spread in α-elements for inhomogeneous models agrees with observations and whether this provides constraints on supernova explosion models and their nucleosynthesis.

  5. Supercritical carbon dioxide-processed resorbable polymer nanocomposites for bone graft substitute applications

    NASA Astrophysics Data System (ADS)

    Baker, Kevin C.

    Numerous clinical situations necessitate the use of bone graft materials to enhance bone formation. While autologous and allogenic materials are considered the gold standards in the setting of fracture healing and spine fusion, their disadvantages, which include donor site morbidity and finite supply have stimulated research and development of novel bone graft substitute materials. Among the most promising candidate materials are resorbable polymers, composed of lactic and/or glycolic acid. While the characteristics of these materials, such as predictable degradation kinetics and biocompatibility, make them an excellent choice for bone graft substitute applications, they lack mechanical strength when synthesized with the requisite porous morphology. As such, porous resorbable polymers are often reinforced with filler materials. In the presented work, we describe the use of supercritical carbon dioxide (scCO2) processing to create porous resorbable polymeric constructs reinforced by nanostructured, organically modified Montmorillonite clay (nanoclay). scCO2 processing simultaneously disperses the nanoclay throughout the polymeric matrix, while imparting a porous morphology to the construct conducive to facilitating cellular infiltration and neoangiogenesis, which are necessary components of bone growth. With the addition of as little as 2.5wt% of nanoclay, the compressive strength of the constructs nearly doubles putting them on par with human cortico-cancellous bone. Rheological measurements indicate that the dominant mode of reinforcement of the nanocomposite constructs is the restriction of polymer chain mobility. This restriction is a function of the positive interaction between polymer chains and the nanoclay. In vivo inflammation studies indicate biocompatibility of the constructs. Ectopic osteogenesis assays have determined that the scCO2-processed nanocomposites are capable of supporting growth-factor induced bone formation. scCO 2-processed resorbable

  6. CO2 Capture and Regeneration at Low Temperatures: Novel Non-Aqueous CO2 Solvents and Capture Process with Substantially Reduced Energy Penalties

    SciTech Connect

    2010-07-01

    IMPACCT Project: RTI is developing a solvent and process that could significantly reduce the temperature associated with regenerating solvent and CO2 captured from the exhaust gas of coal-fired power plants. Traditional CO2 removal processes using water-based solvents require significant amount of steam from power plants in order to regenerate the solvent so it can be reused after each reaction. RTI’s solvents can be better at absorbing CO2 than many water-based solvents, and are regenerated at lower temperatures using less steam. Thus, industrial heat that is normally too cool to re-use can be deployed for regeneration, rather than using high-value steam. This saves the power plant money, which results in increased cost savings for consumers.

  7. Novel shortcut estimation method for regeneration energy of amine solvents in an absorption-based carbon capture process.

    PubMed

    Kim, Huiyong; Hwang, Sung June; Lee, Kwang Soon

    2015-02-01

    Among various CO2 capture processes, the aqueous amine-based absorption process is considered the most promising for near-term deployment. However, the performance evaluation of newly developed solvents still requires complex and time-consuming procedures, such as pilot plant tests or the development of a rigorous simulator. Absence of accurate and simple calculation methods for the energy performance at an early stage of process development has lengthened and increased expense of the development of economically feasible CO2 capture processes. In this paper, a novel but simple method to reliably calculate the regeneration energy in a standard amine-based carbon capture process is proposed. Careful examination of stripper behaviors and exploitation of energy balance equations around the stripper allowed for calculation of the regeneration energy using only vapor-liquid equilibrium and caloric data. Reliability of the proposed method was confirmed by comparing to rigorous simulations for two well-known solvents, monoethanolamine (MEA) and piperazine (PZ). The proposed method can predict the regeneration energy at various operating conditions with greater simplicity, greater speed, and higher accuracy than those proposed in previous studies. This enables faster and more precise screening of various solvents and faster optimization of process variables and can eventually accelerate the development of economically deployable CO2 capture processes.

  8. Digital image capture, processing, and recording system upgrade for the APS-94F SLAR

    NASA Astrophysics Data System (ADS)

    Ferraris, Guillermo L.

    2000-11-01

    The Argentine Army has been operating the APS-94F SLAR systems, on board the venerable OV-1D MOHAWK aircraft, since 1996. These systems were received from the U.S. Government through the FMS program. One major handicap of the system is due to the now obsolete imagery recording subsystem, which includes complex optical, thermal and electro-mechanical obsolete processes and components, that account for most of the degradations and distortions in the images obtained (not to mention the fact that images are recorded on a 9.5-inch silver halide film media, which has to be kept at -17 degree(s)C and has to be brought to thermal equilibrium with the environment eight hours before the mission). An integral digital capture, processing and recording subsystem was developed at CITEFA (Instituto de Investigaciones Cientificas y Tecnicas de las Fuerzas Armadas) to replace the old analog RO-495/U recorder, as an upgrade to this very robust and proven imaging radar system The subsystem developed includes three custom designed ISA boards: (1) Radar video and aircraft attitude signal conditioning board, (2) Microprocessor controlled two- channel high speed digitizing board and (3) Integrated 12- channel GPS OEM board. The operator's software interface is a PC based GUI C++ application, including radar imagery forming and processing algorithms, slant range to ground range conversion, digitally controlled image gain, bias and contrast adjustments, image registration (GPS), image file disk recording and retrieval functions, real time mensuration and MTI/FTI (moving target indication/fixed target indication) image correlation. The system also provides for the added capability to send compressed still radar images in NRT (near real time) to a ground receiving station through a secure data link. Due to serious space limitations inside the OV-1D two-seat cockpit, a military grade ruggedized laptop computer and docking station hardware implementation was selected.

  9. Fabrication of micro-hollow fiber by electrospinning process in near-critical carbon dioxide

    SciTech Connect

    Okamoto, Koichi; Wahyudiono,; Kanda, Hideki; Goto, Motonobu; Machmudah, Siti; Okubayashi, Satoko; Fukuzato, Ryuichi

    2014-02-24

    Electrospinning is a simple technique that has gained much attention because of its capability and feasibility in the fabrication of large quantities of fibers from polymer with diameters ranging in nano-microscale. These fibers provided high surface area to volume ratios, and it was of considerable interest for many applications, such as nanoparticle carriers in controlled release, scaffolds in tissue engineering, wound dressings, military wear with chemical and biological toxin-resistance, nanofibrous membranes or filters, and electronic sensors. Recently there has been a great deal of progress in the potential applications of hollow fibers in microfluids, photonics, and energy storage. In this work, electrospinning was conducted under high-pressure carbon dioxide (CO{sub 2}) to reduce the viscosity of polymer solution. The experiments were conducted at 313 K and ∼8.0 MPa. Polymer solution containing 5 wt% polymers which prepared in dichloromethane (DCM) with polyvinylpyrrolidone (PVP) to poly-L-lactic acid (PLLA) ratio 80:20 was used as a feed solution. The applied voltage was 15 kV and the distance of nozzle and collector was 8 cm. The morphology and structure of the fibers produced were observed using scanning electron microscopy (SEM). Under pressurized CO{sub 2}, PVP electrospun was produced without bead formation with diameter ranges of 608.50 - 7943.19 nm. These behaviors hold the potential to considerably improve devolatilization electrospinning processes.

  10. Carbon Dioxide Convection in the Martian Polar Night and Its Implications for Polar Processes

    NASA Technical Reports Server (NTRS)

    Colaprete, A.; Haberle, R. M.

    2003-01-01

    Each Martian year nearly 30% of the atmosphere is exchanged with the polar ice caps. This exchange occurs through a combination of direct surface condensation and atmospheric precipitation of carbon dioxide. It has long been thought the amount of condensation within the polar night is maintained by a balance between diabatic processes such as radiative cooling and latent heating from condensing CO2. This assumption manifests itself in Mars General Circulation Models (GCM) in such a way as to never allow the atmospheric temperature to dip below the saturation temperature of CO2. However, observations from Mars Global Surveyor (MGS) Radio Science (RS) and the Thermal Emission Spectrometer (TES) have demonstrated this assumption to be, at best, approximate. Both RS and TES observations within the polar nights of both poles indicate substantial supersaturated regions with respect to CO2. The observed temperature profiles suggest conditionally unstable regions containing planetary significant amounts of potential convective energy. Presented here are estimates of the total planetary inventory of convective available potential energy (CAPE) and the potential convective energy flux (PCEF). The values for CAPE and PCEF are derived from RS temperature profiles and compared to Mars GCM results using a new convective CO2 cloud model that allows for the formation of CAPE.

  11. Specific capture of the hydrolysate on magnetic beads for sensitive detecting plant vacuolar processing enzyme activity.

    PubMed

    Zhou, Jun; Cheng, Meng; Zeng, Lizhang; Liu, Weipeng; Zhang, Tao; Xing, Da

    2016-05-15

    Conventional plant protease detection always suffers from high background interference caused by the complex coloring metabolites in plant cells. In this study, a bio-modified magnetic beads-based strategy was developed for sensitive and quantitative detection of plant vacuolar processing enzyme (VPE) activity. Cleavage of the peptide substrate (ESENCRK-FITC) after asparagine residue by VPE resulted in the 2-cyano-6-amino-benzothiazole (CABT)-functionalized magnetic beads capture of the severed substrate CRK-FITC via a condensation reaction between CABT and cysteine (Cys). The catalytic activity was subsequently obtained by the confocal microscopy imaging and flow cytometry quantitative analysis. The sensor system integrated advantages of (i) the high efficient enrichment and separation capabilities of magnetic beads and (ii) the catalyst-free properties of the CABT-Cys condensation reaction. It exhibited a linear relationship between the fluorescence signal and the concentration of severed substrate in the range of 10-600 pM. The practical results showed that, compared with normal growth conditions, VPE activity was increased by 2.7-fold (307.2 ± 25.3 μM min(-1)g(-1)) upon cadmium toxicity stress. This platform effectively overcame the coloring metabolites-caused background interference, showing fine applicability for the detection of VPE activity in real samples. The strategy offers great sensitivity and may be further extended to other protease activity detection. PMID:26797250

  12. Production of heavy and superheavy neutron-rich nuclei in neutron capture processes

    NASA Astrophysics Data System (ADS)

    Zagrebaev, V. I.; Karpov, A. V.; Mishustin, I. N.; Greiner, Walter

    2011-10-01

    The neutron capture process is considered as an alternative method for production of superheavy (SH) nuclei. Strong neutron fluxes might be provided by nuclear reactors and nuclear explosions in the laboratory frame and by supernova explosions in nature. All these cases are discussed in the paper. There are two gaps of short-lived nuclei (one is the well-known fermium gap and the other one is located in the region of Z=106-108 and N˜170) which impede the formation of SH nuclei by rather weak neutron fluxes realized at available nuclear reactors. We find that in the course of multiple (rather “soft”) nuclear explosions these gaps may be easily bypassed, and thus, a measurable amount of the neutron-rich long-living SH nuclei located at the island of stability may be synthesized. Existing pulsed reactors do not allow one to bypass these gaps. We formulate requirements for the pulsed reactors of the next generation that could be used for production of long-living SH nuclei. Natural formation of SH nuclei (in supernova explosions) is also discussed. The yield of SH nuclei relative to lead is estimated to be about 10-12, which is not beyond the experimental sensitivity for a search of SH elements in cosmic rays.

  13. ADVANCED OXYFUEL BOILERS AND PROCESS HEATERS FOR COST EFFECTIVE CO{sub 2} CAPTURE AND SEQUESTRATION

    SciTech Connect

    David R. Thompson; Lawrence E. Bool; G. Maxwell Christie

    2003-07-01

    This annual technical progress report summarizes the work accomplished during the first year of the program, January-December 2002, in the following task areas: Task 1--Conceptual Design, Task 2--Laboratory Scale Evaluations, Task 3--OTM Development, Task 4--Economic Evaluation and Commercialization Planning and Task 5--Program Management. The program has experienced significant delays due to several factors. The budget has also been significantly under spent. Based on recent technical successes significant future progress is expected. A number of concepts for integrating Oxygen Transport Membranes (OTMs) into boilers and process heaters to facilitate oxy-fuel combustion have been proposed. A detailed modeling plan has been proposed and early modeling work has focused on developing spreadsheet based models for quick engineering calculations. Combustion reactor laboratory scale evaluations efforts have been delayed due to the closing of Praxair's Tarrytown facility in December 2001. Experimental facilities and personnel have been relocated to Praxair's facility in Tonawanda. The facilities have recently been re-commissioned. Work with the OTM development task has also been delayed as early material selections were discarded. More recently, more promising OTM material compositions have been identified. Economic evaluation commenced. Information was acquired that quantified the attractiveness of the advanced oxygen-fired boiler. CO{sub 2} capture and compression are still estimated to be much less than $10/ton carbon.

  14. Impact of CO2 leakage from sub-seabed carbon dioxide capture and storage (CCS) reservoirs on benthic virus-prokaryote interactions and functions.

    PubMed

    Rastelli, Eugenio; Corinaldesi, Cinzia; Dell'Anno, Antonio; Amaro, Teresa; Queirós, Ana M; Widdicombe, Stephen; Danovaro, Roberto

    2015-01-01

    Atmospheric CO2 emissions are a global concern due to their predicted impact on biodiversity, ecosystems functioning, and human life. Among the proposed mitigation strategies, CO2 capture and storage, primarily the injection of CO2 into marine deep geological formations has been suggested as a technically practical option for reducing emissions. However, concerns have been raised that possible leakage from such storage sites, and the associated elevated levels of pCO2 could locally impact the biodiversity and biogeochemical processes in the sediments above these reservoirs. Whilst a number of impact assessment studies have been conducted, no information is available on the specific responses of viruses and virus-host interactions. In the present study, we tested the impact of a simulated CO2 leakage on the benthic microbial assemblages, with specific focus on microbial activity and virus-induced prokaryotic mortality (VIPM). We found that exposure to levels of CO2 in the overlying seawater from 1,000 to 20,000 ppm for a period up to 140 days, resulted in a marked decrease in heterotrophic carbon production and organic matter degradation rates in the sediments, associated with lower rates of VIPM, and a progressive accumulation of sedimentary organic matter with increasing CO2 concentrations. These results suggest that the increase in seawater pCO2 levels that may result from CO2 leakage, can severely reduce the rates of microbial-mediated recycling of the sedimentary organic matter and viral infections, with major consequences on C cycling and nutrient regeneration, and hence on the functioning of benthic ecosystems.

  15. Impact of CO2 leakage from sub-seabed carbon dioxide capture and storage (CCS) reservoirs on benthic virus–prokaryote interactions and functions

    PubMed Central

    Rastelli, Eugenio; Corinaldesi, Cinzia; Dell’Anno, Antonio; Amaro, Teresa; Queirós, Ana M.; Widdicombe, Stephen; Danovaro, Roberto

    2015-01-01

    Atmospheric CO2 emissions are a global concern due to their predicted impact on biodiversity, ecosystems functioning, and human life. Among the proposed mitigation strategies, CO2 capture and storage, primarily the injection of CO2 into marine deep geological formations has been suggested as a technically practical option for reducing emissions. However, concerns have been raised that possible leakage from such storage sites, and the associated elevated levels of pCO2 could locally impact the biodiversity and biogeochemical processes in the sediments above these reservoirs. Whilst a number of impact assessment studies have been conducted, no information is available on the specific responses of viruses and virus–host interactions. In the present study, we tested the impact of a simulated CO2 leakage on the benthic microbial assemblages, with specific focus on microbial activity and virus-induced prokaryotic mortality (VIPM). We found that exposure to levels of CO2 in the overlying seawater from 1,000 to 20,000 ppm for a period up to 140 days, resulted in a marked decrease in heterotrophic carbon production and organic matter degradation rates in the sediments, associated with lower rates of VIPM, and a progressive accumulation of sedimentary organic matter with increasing CO2 concentrations. These results suggest that the increase in seawater pCO2 levels that may result from CO2 leakage, can severely reduce the rates of microbial-mediated recycling of the sedimentary organic matter and viral infections, with major consequences on C cycling and nutrient regeneration, and hence on the functioning of benthic ecosystems. PMID:26441872

  16. Nitrogen dioxide

    Integrated Risk Information System (IRIS)

    Nitrogen dioxide ; CASRN 10102 - 44 - 0 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogeni

  17. Chlorine dioxide

    Integrated Risk Information System (IRIS)

    Chlorine dioxide ; CASRN 10049 - 04 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogeni

  18. Sea surface carbon dioxide at the Georgia time series site (2006-2007): Air-sea flux and controlling processes

    NASA Astrophysics Data System (ADS)

    Xue, Liang; Cai, Wei-Jun; Hu, Xinping; Sabine, Christopher; Jones, Stacy; Sutton, Adrienne J.; Jiang, Li-Qing; Reimer, Janet J.

    2016-01-01

    Carbon dioxide partial pressure (pCO2) in surface seawater was continuously recorded every three hours from 18 July 2006 through 31 October 2007 using a moored autonomous pCO2 (MAPCO2) system deployed on the Gray's Reef buoy off the coast of Georgia, USA. Surface water pCO2 (average 373 ± 52 μatm) showed a clear seasonal pattern, undersaturated with respect to the atmosphere in cold months and generally oversaturated in warm months. High temporal resolution observations revealed important events not captured in previous ship-based observations, such as sporadically occurring biological CO2 uptake during April-June 2007. In addition to a qualitative analysis of the primary drivers of pCO2 variability based on property regressions, we quantified contributions of temperature, air-sea exchange, mixing, and biological processes to monthly pCO2 variations using a 1-D mass budget model. Although temperature played a dominant role in the annual cycle of pCO2, river inputs especially in the wet season, biological respiration in peak summer, and biological production during April-June 2007 also substantially influenced seawater pCO2. Furthermore, sea surface pCO2 was higher in September-October 2007 than in September-October 2006, associated with increased river inputs in fall 2007. On an annual basis this site was a moderate atmospheric CO2 sink, and was autotrophic as revealed by monthly mean net community production (NCP) in the mixed layer. If the sporadic short productive events during April-May 2007 were missed by the sampling schedule, one would conclude erroneously that the site is heterotrophic. While previous ship-based pCO2 data collected around this buoy site agreed with the buoy CO2 data on seasonal scales, high resolution buoy observations revealed that the cruise-based surveys undersampled temporal variability in coastal waters, which could greatly bias the estimates of air-sea CO2 fluxes or annual NCP, and even produce contradictory results.

  19. Carbon dioxide absorbent and method of using the same

    DOEpatents

    Perry, Robert James; Lewis, Larry Neil; O'Brien, Michael Joseph; Soloveichik, Grigorii Lev; Kniajanski, Sergei; Lam, Tunchiao Hubert; Lee, Julia Lam; Rubinsztajn, Malgorzata Iwona

    2011-10-04

    In accordance with one aspect, the present invention provides an amino-siloxane composition comprising at least one of structures I, II, III, IV or V said compositions being useful for the capture of carbon dioxide from gas streams such as power plant flue gases. In addition, the present invention provides methods of preparing the amino-siloxane compositions are provided. Also provided are methods for reducing the amount of carbon dioxide in a process stream employing the amino-siloxane compositions of the invention as species which react with carbon dioxide to form an adduct with carbon dioxide. The reaction of the amino-siloxane compositions provided by the present invention with carbon dioxide is reversible and thus, the method provides for multicycle use of said compositions.

  20. Catalytic dehydrogenation of propane by carbon dioxide: a medium-temperature thermochemical process for carbon dioxide utilisation.

    PubMed

    Du, X; Yao, B; Gonzalez-Cortes, S; Kuznetsov, V L; AlMegren, Hamid; Xiao, T; Edwards, P P

    2015-01-01

    The dehydrogenation of C3H8 in the presence of CO2 is an attractive catalytic route for C3H6 production. In studying the various possibilities to utilise CO2 to convert hydrocarbons using the sustainable energy source of solar thermal energy, thermodynamic calculations were carried out for the dehydrogenation of C3H8 using CO2for the process operating in the temperature range of 300-500 °C. Importantly, the results highlight the enhanced potential of C3H8 as compared to its lighter and heavier homologues (C2H6 and C4H10, respectively). To be utilised in this CO2 utilisation reaction the Gibbs free energy (ΔrGθm) of each reaction in the modelled, complete reacting system of the dehydrogenation of C3H8 in the presence of CO2 also indicate that further cracking of C3H6 will affect the ultimate yield and selectivity of the final products. In a parallel experimental study, catalytic tests of the dehydrogenation of C3H8 in the presence of CO2 over 5 wt%-Cr2O3/ZrO2 catalysts operating at 500 °C, atmospheric pressure, and for various C3H8 partial pressures and various overall GHSV (Gas Hourly Space Velocity) values. The results showed that an increase in the C3H8 partial pressure produced an inhibition of C3H8 conversion but, importantly, a promising enhancement of C3H6 selectivity. This phenomenon can be attributed to competitive adsorption on the catalyst between the generated C3H6 and inactivated C3H8, which inhibits any further cracking effect on C3H6 to produce by-products. As a comparison, the increase of the overall GHSV can also decrease the C3H8 conversion to a similar extent, but the further cracking of C3H6 cannot be limited. PMID:26392020

  1. A survey on sensor coverage and visual data capturing/processing/transmission in wireless visual sensor networks.

    PubMed

    Yap, Florence G H; Yen, Hong-Hsu

    2014-01-01

    Wireless Visual Sensor Networks (WVSNs) where camera-equipped sensor nodes can capture, process and transmit image/video information have become an important new research area. As compared to the traditional wireless sensor networks (WSNs) that can only transmit scalar information (e.g., temperature), the visual data in WVSNs enable much wider applications, such as visual security surveillance and visual wildlife monitoring. However, as compared to the scalar data in WSNs, visual data is much bigger and more complicated so intelligent schemes are required to capture/process/ transmit visual data in limited resources (hardware capability and bandwidth) WVSNs. WVSNs introduce new multi-disciplinary research opportunities of topics that include visual sensor hardware, image and multimedia capture and processing, wireless communication and networking. In this paper, we survey existing research efforts on the visual sensor hardware, visual sensor coverage/deployment, and visual data capture/ processing/transmission issues in WVSNs. We conclude that WVSN research is still in an early age and there are still many open issues that have not been fully addressed. More new novel multi-disciplinary, cross-layered, distributed and collaborative solutions should be devised to tackle these challenging issues in WVSNs. PMID:24561401

  2. A Survey on Sensor Coverage and Visual Data Capturing/Processing/Transmission in Wireless Visual Sensor Networks

    PubMed Central

    Yap, Florence G. H.; Yen, Hong-Hsu

    2014-01-01

    Wireless Visual Sensor Networks (WVSNs) where camera-equipped sensor nodes can capture, process and transmit image/video information have become an important new research area. As compared to the traditional wireless sensor networks (WSNs) that can only transmit scalar information (e.g., temperature), the visual data in WVSNs enable much wider applications, such as visual security surveillance and visual wildlife monitoring. However, as compared to the scalar data in WSNs, visual data is much bigger and more complicated so intelligent schemes are required to capture/process/transmit visual data in limited resources (hardware capability and bandwidth) WVSNs. WVSNs introduce new multi-disciplinary research opportunities of topics that include visual sensor hardware, image and multimedia capture and processing, wireless communication and networking. In this paper, we survey existing research efforts on the visual sensor hardware, visual sensor coverage/deployment, and visual data capture/processing/transmission issues in WVSNs. We conclude that WVSN research is still in an early age and there are still many open issues that have not been fully addressed. More new novel multi-disciplinary, cross-layered, distributed and collaborative solutions should be devised to tackle these challenging issues in WVSNs. PMID:24561401

  3. A survey on sensor coverage and visual data capturing/processing/transmission in wireless visual sensor networks.

    PubMed

    Yap, Florence G H; Yen, Hong-Hsu

    2014-02-20

    Wireless Visual Sensor Networks (WVSNs) where camera-equipped sensor nodes can capture, process and transmit image/video information have become an important new research area. As compared to the traditional wireless sensor networks (WSNs) that can only transmit scalar information (e.g., temperature), the visual data in WVSNs enable much wider applications, such as visual security surveillance and visual wildlife monitoring. However, as compared to the scalar data in WSNs, visual data is much bigger and more complicated so intelligent schemes are required to capture/process/ transmit visual data in limited resources (hardware capability and bandwidth) WVSNs. WVSNs introduce new multi-disciplinary research opportunities of topics that include visual sensor hardware, image and multimedia capture and processing, wireless communication and networking. In this paper, we survey existing research efforts on the visual sensor hardware, visual sensor coverage/deployment, and visual data capture/ processing/transmission issues in WVSNs. We conclude that WVSN research is still in an early age and there are still many open issues that have not been fully addressed. More new novel multi-disciplinary, cross-layered, distributed and collaborative solutions should be devised to tackle these challenging issues in WVSNs.

  4. Effect of water on the physical properties and carbon dioxide capture capacities of liquid-like Nanoparticle Organic Hybrid Materials and their corresponding polymers.

    PubMed

    Petit, Camille; Bhatnagar, Sonali; Park, Ah-Hyung Alissa

    2013-10-01

    Binary systems composed of liquid-like Nanoparticle Organic Hybrid Materials (NOHMs) and the secondary fluid (i.e., water) were prepared, and their thermal stabilities, densities, viscosities, and CO2 absorption capacities were investigated. Recent work has suggested NOHMs as an alternative CO2 capture media with interesting chemical and physical tunability. Anhydrous CO2 capture solvents often degrade when they are exposed to water, while flue gas generally contains about 8-16% water. Thus, this study was conducted to investigate the effect of water on the NOHMs' properties relevant to CO2 capture as well as the chemical and thermal stabilities of H2O-loaded NOHMs. It was found that water acted as an antisolvent of NOHMs, and therefore, caused a decreased CO2 capture capacity. On the other hand, the results indicated that while water did not affect the NOHMs' thermal stability, it significantly helped lowering their density and viscosity. In order to investigate the effect of intermolecular interactions among two fluids on the density and viscosity, the excess volumes and viscosity deviations were calculated and correlated with Redlich-Kister equations. The trends revealed the existence of strong intermolecular interactions between water molecules and the poly(ethlyne glycol) component of NOHMs, which may have caused the drastic decrease in the NOHMs' viscosity with the addition of water.

  5. Cell migration and antigen capture are antagonistic processes coupled by myosin II in dendritic cells

    PubMed Central

    Chabaud, Mélanie; Heuzé, Mélina L.; Bretou, Marine; Vargas, Pablo; Maiuri, Paolo; Solanes, Paola; Maurin, Mathieu; Terriac, Emmanuel; Le Berre, Maël; Lankar, Danielle; Piolot, Tristan; Adelstein, Robert S.; Zhang, Yingfan; Sixt, Michael; Jacobelli, Jordan; Bénichou, Olivier; Voituriez, Raphaël; Piel, Matthieu; Lennon-Duménil, Ana-Maria

    2015-01-01

    The immune response relies on the migration of leukocytes and on their ability to stop in precise anatomical locations to fulfil their task. How leukocyte migration and function are coordinated is unknown. Here we show that in immature dendritic cells, which patrol their environment by engulfing extracellular material, cell migration and antigen capture are antagonistic. This antagonism results from transient enrichment of myosin IIA at the cell front, which disrupts the back-to-front gradient of the motor protein, slowing down locomotion but promoting antigen capture. We further highlight that myosin IIA enrichment at the cell front requires the MHC class II-associated invariant chain (Ii). Thus, by controlling myosin IIA localization, Ii imposes on dendritic cells an intermittent antigen capture behaviour that might facilitate environment patrolling. We propose that the requirement for myosin II in both cell migration and specific cell functions may provide a general mechanism for their coordination in time and space. PMID:26109323

  6. Green Catalytic Process for Cyclic Carbonate Synthesis from Carbon Dioxide under Mild Conditions.

    PubMed

    Lang, Xian-Dong; He, Liang-Nian

    2016-06-01

    As a renewable and abundant C1 resource possessing multiple attractive characteristics, such as low cost, nontoxicity, non-flammability, and easy accessibility, CO2 conversion into value-added chemicals and fuels can contribute to green chemistry and sustainable development. Since CO2 is a thermodynamically inert molecule, the activation of CO2 is pivotal for its effective conversion. In this regard, the formation of a transition-metal CO2 complex through direct coordination is one of the most powerful ways to induce the inert CO2 molecule to undergo chemical reactions. To date, numerous processes have been developed for efficient synthesis of cyclic carbonates from CO2 . On the basis of mechanistic understanding, we have developed efficient metal catalysts and green processes, including heterogeneous catalysis, and metal-free systems, such as ionic liquids, for cyclic carbonate synthesis. The big challenge is to develop catalysts that promote the reaction under low pressure (preferably at 1 bar). In this context, bifunctional catalysis is capable of synergistic activation of both the substrate and CO2 molecule, and thus, could render CO2 conversion smoothly under mild conditions. Alternatively, converting CO2 derivatives, that is, the captured CO2 as an activated species, would more easily take place at low pressure in comparison with gaseous CO2 . The aim of this Personal Account is to summarize versatile catalytic processes for cyclic carbonate synthesis from CO2 , including epoxide/CO2 coupling reaction, carboxylation of 1,2-diol with CO2 , oxidative cyclization of olefins with CO2 , condensation of vicinal halohydrin with CO2 , carboxylative cyclization of propargyl alcohols with CO2 , and conversion of the CO2 derivatives. PMID:27121768

  7. Mixed uranium dicarbide and uranium dioxide microspheres and process of making same

    DOEpatents

    Stinton, David P.

    1983-01-01

    Nuclear fuel microspheres are made by sintering microspheres containing uranium dioxide and uncombined carbon in a 1 mole percent carbon monoxide/99 mole percent argon atmosphere at 1550.degree. C. and then sintering the microspheres in a 3 mole percent carbon monoxide/97 mole percent argon atmosphere at the same temperature.

  8. A polyhedral metal-organic framework based on the supermolecular building block strategy exhibiting high performance for carbon dioxide capture and separation of light hydrocarbons.

    PubMed

    Wang, Dongmei; Liu, Bing; Yao, Shuo; Wang, Tao; Li, Guanghua; Huo, Qisheng; Liu, Yunling

    2015-10-25

    By using the supermolecular building block (SBB) strategy, a polyhedron-based metal-organic framework (PMOF), which features three types of cages with multiple sizes and shapes, has been synthesized. It exhibits high performance for CO2 capture (170 cm(3) g(-1) at 273 K under 1 bar) and selectivity of CO2/CH4 (9.4) and C3H8/CH4 (271.5).

  9. Electricity from fossil fuels without CO2 emissions: assessing the costs of carbon dioxide capture and sequestration in U.S. electricity markets.

    PubMed

    Johnson, T L; Keith, D W

    2001-10-01

    The decoupling of fossil-fueled electricity production from atmospheric CO2 emissions via CO2 capture and sequestration (CCS) is increasingly regarded as an important means of mitigating climate change at a reasonable cost. Engineering analyses of CO2 mitigation typically compare the cost of electricity for a base generation technology to that for a similar plant with CO2 capture and then compute the carbon emissions mitigated per unit of cost. It can be hard to interpret mitigation cost estimates from this plant-level approach when a consistent base technology cannot be identified. In addition, neither engineering analyses nor general equilibrium models can capture the economics of plant dispatch. A realistic assessment of the costs of carbon sequestration as an emissions abatement strategy in the electric sector therefore requires a systems-level analysis. We discuss various frameworks for computing mitigation costs and introduce a simplified model of electric sector planning. Results from a "bottom-up" engineering-economic analysis for a representative U.S. North American Electric Reliability Council (NERC) region illustrate how the penetration of CCS technologies and the dispatch of generating units vary with the price of carbon emissions and thereby determine the relationship between mitigation cost and emissions reduction.

  10. Laser capture.

    PubMed

    Potter, S Steven; Brunskill, Eric W

    2012-01-01

    This chapter describes detailed methods used for laser capture microdissection (LCM) of discrete subpopulations of cells. Topics covered include preparing tissue blocks, cryostat sectioning, processing slides, performing the LCM, and purification of RNA from LCM samples. Notes describe the fine points of each operation, which can often mean the difference between success and failure. PMID:22639264

  11. Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

    SciTech Connect

    Wood, Benjamin; Genovese, Sarah; Perry, Robert; Spiry, Irina; Farnum, Rachael; Sing, Surinder; Wilson, Paul; Buckley, Paul; Acharya, Harish; Chen, Wei; McDermott, John; Vipperia, Ravikumar; Yee, Michael; Steele, Ray; Fresia, Megan; Vogt, Kirk

    2013-12-31

    A bench-scale system was designed and built to test an aminosilicone-based solvent. A model was built of the bench-scale system and this model was scaled up to model the performance of a carbon capture unit, using aminosilicones, for CO{sub 2} capture and sequestration (CCS) for a pulverized coal (PC) boiler at 550 MW. System and economic analysis for the carbon capture unit demonstrates that the aminosilicone solvent has significant advantages relative to a monoethanol amine (MEA)-based system. The CCS energy penalty for MEA is 35.9% and the energy penalty for aminosilicone solvent is 30.4% using a steam temperature of 395 °C (743 °F). If the steam temperature is lowered to 204 °C (400 °F), the energy penalty for the aminosilicone solvent is reduced to 29%. The increase in cost of electricity (COE) over the non-capture case for MEA is ~109% and increase in COE for aminosilicone solvent is ~98 to 103% depending on the solvent cost at a steam temperature of 395 °C (743 °F). If the steam temperature is lowered to 204 °C (400 °F), the increase in COE for the aminosilicone solvent is reduced to ~95-100%.

  12. The Impact of Electric Passenger Transport Technology under an Economy-Wide Climate Policy in the United States: Carbon Dioxide Emissions, Coal Use, and Carbon Dioxide Capture and Storage

    SciTech Connect

    Wise, Marshall A.; Kyle, G. Page; Dooley, James J.; Kim, Son H.

    2010-03-01

    Plug-in hybrid electric vehicles (PHEVs) have the potential to be an economic means of reducing direct (or tailpipe) carbon dioxide (CO2) emissions from the transportation sector. However, without a climate policy that places a limit on CO2 emissions from the electric generation sector, the net impact of widespread deployment of PHEVs on overall U.S. CO2 emissions is not as clear. A comprehensive analysis must consider jointly the transportation and electricity sectors, along with feedbacks to the rest of the energy system. In this paper, we use the Pacific Northwest National Laboratory’s MiniCAM model to perform an integrated economic analysis of the penetration of PHEVs and the resulting impact on total U.S. CO2 emissions.

  13. Continuous bind-and-elute protein A capture chromatography: Optimization under process scale column constraints and comparison to batch operation.

    PubMed

    Kaltenbrunner, Oliver; Diaz, Luis; Hu, Xiaochun; Shearer, Michael

    2016-07-01

    Recently, continuous downstream processing has become a topic of discussion and analysis at conferences while no industrial applications of continuous downstream processing for biopharmaceutical manufacturing have been reported. There is significant potential to increase the productivity of a Protein A capture step by converting the operation to simulated moving bed (SMB) mode. In this mode, shorter columns are operated at higher process flow and corresponding short residence times. The ability to significantly shorten the product residence time during loading without appreciable capacity loss can dramatically increase productivity of the capture step and consequently reduce the amount of Protein A resin required in the process. Previous studies have not considered the physical limitations of how short columns can be packed and the flow rate limitations due to pressure drop of stacked columns. In this study, we are evaluating the process behavior of a continuous Protein A capture column cycling operation under the known pressure drop constraints of a compressible media. The results are compared to the same resin operated under traditional batch operating conditions. We analyze the optimum system design point for a range of feed concentrations, bed heights, and load residence times and determine achievable productivity for any feed concentration and any column bed height. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:938-948, 2016. PMID:27111828

  14. New insights on Ba overabundance in open clusters. Evidence for the intermediate neutron-capture process at play?

    NASA Astrophysics Data System (ADS)

    Mishenina, T.; Pignatari, M.; Carraro, G.; Kovtyukh, V.; Monaco, L.; Korotin, S.; Shereta, E.; Yegorova, I.; Herwig, F.

    2015-02-01

    Recently, an increasing number of studies were devoted to measure the abundances of neutron-capture elements heavier than iron in stars belonging to Galactic Open Clusters (OCs). OCs span a sizeable range in metallicity (-0.6 ≤ [Fe/H] ≤ +0.4), and they show abundances of light elements similar to disc stars of the same age. A different pattern is observed for heavy elements. A large scatter is observed for Ba, with most OCs showing [Ba/Fe] and [Ba/La] overabundant with respect to the Sun. The origin of this overabundance is not clearly understood. With the goal of providing new observational insights, we determined radial velocities, atmospheric parameters and chemical composition of 27 giant stars members of five OCs: Cr 110, Cr 261, NGC 2477, NGC 2506 and NGC 5822. We used high-resolution spectra obtained with the UVES spectrograph at European Southern Observatory Paranal. We perform a detailed spectroscopic analysis of these stars to measure the abundance of up to 22 elements per star. We study the dependence of element abundance on metallicity and age with unprecedented detail, complementing our analysis with data culled from the literature. We confirm the trend of Ba overabundance in OCs, and show its large dispersion for clusters younger than ˜4 Gyr. Finally, the implications of our results for stellar nucleosynthesis are discussed. We show in this work that the Ba enrichment compared to other neutron-capture elements in OCs cannot be explained by the contributions from the slow neutron-capture process and the rapid neutron-capture process. Instead, we argue that this anomalous signature can be explained by assuming an additional contribution by the intermediate neutron-capture process.

  15. Synthesis of a novel β-ketoenamine-linked conjugated microporous polymer with Nsbnd H functionalized pore surface for carbon dioxide capture

    NASA Astrophysics Data System (ADS)

    Shuangzhi, Chai; Liu, Haohan; Zhang, Xue; Han, Yang; Hu, Nantao; Wei, Liangming; Cong, Fengsong; Wei, Hao; Wang, Lin

    2016-10-01

    A novel β-ketoenamine-linked conjugated microporous polymer (KECMP-1) was synthesized via Schiff base condensation between 1,3,5-triformylphloroglucinol and m-phenylenediamine by conventional solvothermal synthesis without a template or a metal catalyst. KECMP-1 exhibits a considerable Brunauer-Emmett-Teller specific surface area (691 m2 g-1) and high physicochemical stability. By utilizing the bottom-up strategy, the surfaces of the pore walls were covered with the Nsbnd H sites, together with their microporous structures, lead to the high carbon dioxide (CO2) adsorption capability (10.5 wt% at 273 K and 1.0 bar) and heat of adsorption (34.6 kJ mol-1).

  16. Shelf-life extension of minimally processed carrots by gaseous chlorine dioxide.

    PubMed

    Gómez-López, V M; Devlieghere, F; Ragaert, P; Debevere, J

    2007-05-10

    Chlorine dioxide (ClO(2)) gas is a strong oxidizing and sanitizing agent that has a broad and high biocidal effectiveness and big penetration ability; its efficacy to prolong the shelf-life of a minimally processed (MP) vegetable, grated carrots (Daucus carota L.), was tested in this study. Carrots were sorted, their ends removed, hand peeled, cut, washed, spin dried and separated in 2 portions, one to be treated with ClO(2) gas and the other to remain untreated for comparisons. MP carrots were decontaminated in a cabinet at 91% relative humidity and 28 degrees C for up to 6 min, including 30 s of ClO(2) injection to the cabinet, then stored under equilibrium modified atmosphere (4.5% O(2), 8.9% CO(2), 86.6% N(2)) at 7 degrees C for shelf-life studies. ClO(2) concentration in the cabinet rose to 1.33 mg/l after 30 s of treatment, and then fell to nil before 6 min. The shelf-life study included: O(2) and CO(2) headspace concentrations, microbiological quality (mesophilic aerobic bacteria, psychrotrophs, lactic acid bacteria, and yeasts), sensory quality (odour, flavour, texture, overall visual quality, and white blushing), and pH. ClO(2) did not affect respiration rate of MP carrots significantly (alpha< or =0.05), and lowered the pH significantly (alpha< or =0.05). The applied packaging configuration kept O(2) headspace concentrations in treated samples in equilibrium and prevented CO(2) accumulation. After ClO(2) treatment, the decontamination levels (log CFU/g) achieved were 1.88, 1.71, 2.60, and 0.66 for mesophilic aerobic bacteria, psychrotrophs, and yeasts respectively. The initial sensory quality of MP carrots was not impaired significantly (alpha< or =0.05). A lag phase of at least 2 days was observed for mesophilic aerobic bacteria, psychrotrophs, and lactic acid bacteria in treated samples, while mesophilic aerobic bacteria and psychrotrophs increased parallelly. Odour was the only important attribute in sensory deterioration, but it reached an

  17. Single- and double-electron capture processes in low-energy collisions of N{sup 3+} with He

    SciTech Connect

    Liu, X. J.; Wang, J. G.; Qu, Y. Z.; Buenker, R. J.

    2011-10-15

    Single-electron capture (SEC) and double-electron capture (DEC) processes in collisions of ground state N{sup 3+} (2s{sup 2} {sup 1}S) ions with He are investigated by using the quantum-mechanical molecular-orbital close-coupling (QMOCC) method. The ab initio adiabatic potentials, radial and rotational coupling matrices utilized in QMOCC calculations, are obtained from the multireference single- and double-excitation configuration interaction approach. Total and state-selective SEC and DEC cross sections are presented in the low-energy range from 0.1 eV to 15 keV (i.e., 0.007 eV/u -1.07 keV/u) and rate coefficients in the temperature range from 10{sup 4} to 10{sup 7} K. Our results indicate that the SEC dominates the charge-transfer process in the considered energy region of this collision system and the SEC cross sections are nearly constant in the relatively high-collision energy region, while the DEC cross sections are about 2 orders of magnitude smaller. It is found that, for the SEC processes, in the dominant mechanisms, electrons are captured to exoergic channels N{sup 2+} (2s2p{sup 2} {sup 2}D,{sup 2}S), and for the DEC processes, they are captured to N{sup +} (2s{sup 2}2p{sup 2} {sup 1}D,{sup 1}S). Our calculations also reveal that rotational couplings become important at E > 10 eV/u for SEC and E > 200 eV/u for DEC processes.

  18. Measurement of nitrosamine and nitramine formation from NOx reactions with amines during amine-based carbon dioxide capture for postcombustion carbon sequestration.

    PubMed

    Dai, Ning; Shah, Amisha D; Hu, Lanhua; Plewa, Michael J; McKague, Bruce; Mitch, William A

    2012-09-01

    With years of full-scale experience for precombustion CO(2) capture, amine-based technologies are emerging as the prime contender for postcombustion CO(2) capture. However, concerns for postcombustion applications have focused on the possible contamination of air or drinking water supplies downwind by potentially carcinogenic N-nitrosamines and N-nitramines released following their formation by NO(x) reactions with amines within the capture unit. Analytical methods for N-nitrosamines in drinking waters were adapted to measure specific N-nitrosamines and N-nitramines and total N-nitrosamines in solvent and washwater samples. The high levels of amines, aldehydes, and nitrite in these samples presented a risk for the artifactual formation of N-nitrosamines during sample storage or analysis. Application of a 30-fold molar excess of sulfamic acid to nitrite at pH 2 destroyed nitrite with no significant risk of artifactual nitrosation of amines. Analysis of aqueous morpholine solutions purged with different gas-phase NO and NO(2) concentrations indicated that N-nitrosamine formation generally exceeds N-nitramine formation. The total N-nitrosamine formation rate was at least an order of magnitude higher for the secondary amine piperazine (PZ) than for the primary amines 2-amino-2-methyl-1-propanol (AMP) and monoethanolamine (MEA) and the tertiary amine methyldiethanolamine (MDEA). Analysis of pilot washwater samples indicated a 59 μM total N-nitrosamine concentration for a system operated with a 25% AMP/15% PZ solvent, but only 0.73 μM for a 35% MEA solvent. Unfortunately, a greater fraction of the total N-nitrosamine signal was uncharacterized for the MEA-associated washwater. At a 0.73 μM total N-nitrosamine concentration, a ~25000-fold reduction in concentration is needed between washwater units and downwind drinking water supplies to meet proposed permit limits.

  19. Electron Capture and Its Reverse Process in Hot and Dense Astronuclear Matter

    NASA Astrophysics Data System (ADS)

    Fu, Wei-jie; Wang, Guo-hua; Liu, Yu-xin

    2008-05-01

    Electron capture rate, e-neutrino absorption rate, and e-neutrino absorption mean free path in hot and dense astronuclear matter are calculated in the framework of relativistic mean field (RMF) theory. Their dependence on the density, temperature, and the neutrino abundance of the matter is investigated. We find that the electron capture rate and the neutrino absorption rate are proportional to the cube of the value of the temperature as e-neutrinos are trapped in the stellar matter, and the e-neutrino absorption mean free path is proportional to the inverse of the square of the temperature. The reaction rates increase with the density and the neutrino abundance of the matter. Exact calculation of the reaction rates and the neutrino absorption mean free path is compared with that utilizing the degeneracy approximation. It shows that the latter is inappropriate under the following circumstances: when the stellar matter has a low neutrino abundance, when the density is about or less than the nuclear saturation density, and when the temperature of the matter has a relatively high value, being of the order of 10 MeV or even higher. Kinematically suppressed electron capture or neutrino absorption can be reopened by increasing the temperature of the matter, and its threshold value is about several MeVs when the density of the stellar matter is around the nuclear saturation density. We also discuss the case which is out of beta equilibrium, and the relaxation timescale is estimated. In addition, we show that the strong interactions manifested by the RMF theory decrease the electron capture rate and enlarge the neutrino mean free path if the neutrinos are trapped.

  20. Image Processing Method of the Motion-Capturing PSP/TSP for the Measurement of a Free-Flight Object

    NASA Astrophysics Data System (ADS)

    Ishii, Masato; Goya, Hideki; Miyazaki, Takeshi; Sakaue, Hirotaka

    2015-11-01

    The motion-capturing PSP/TSP system consists of a two-color PSP/TSP and a high-speed color camera. Red and green luminescent images are acquired simultaneously as signal and reference outputs by this system. Simply by rationing the red and the green images, we can obtain a pressure/temperature distribution on the surface of a target object. This system is applied to measure the surface pressure/temperature of a free-flight object. However, an acquired image includes motion blur, focus blur and random noise around the object. We discuss image processing methods and evaluations to optimize those uncertainties. Three types of the edge detect methods are used, which are the sobel, the laplassian and the canny. We will also show the evaluation results to discuss an optimized image processing for the motion-capturing PSP/TSP system.

  1. Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

    SciTech Connect

    Vipperla, Ravikumar; Yee, Michael; Steele, Ray; Singh, Surinder; Spiry, Irina; Wood, Benjamin

    2013-12-30

    This report presents system and economic analysis for a carbon capture unit which uses an amino-silicone solvent for CO{sub 2} capture and sequestration (CCS) in a pulverized coal (PC) boiler. The amino-silicone solvent is based on GAP-1 with tri-ethylene glycol (TEG) as a co-solvent. For comparison purposes, the report also shows results for a CCS unit based on a conventional approach using mono-ethanol amine (MEA). At a steam temperature of 395 °C (743 °F), the CCS energy penalty for amino-silicone solvent is only 30.4% which compares to a 35.9% energy penalty for MEA. The increase in COE for the amino-silicone solvent relative to the non-capture case is between 98% and 103% (depending on the solvent cost) which compares to an ~109% COE cost increase for MEA. In summary, the amino-silicone solvent has significant advantages over conventional systems using MEA.

  2. Processing-property relationships in epoxy resin/titanium dioxide nanocomposites

    SciTech Connect

    Polyzos, Georgios; Tuncer, Enis; Sauers, Isidor; More, Karren Leslie

    2010-01-01

    In situ precipitated titanium dioxide nanoparticles improve the physical properties of polymer composites. Since the pioneering work at Toyota Research Center on exfoliated montmorillonite nanoparticles in a nylon matrix, extensive studies have been performed on polymer nanocomposites in an effort to better integrate organic and inorganic phases. Inorganic fillers, such as silicon and titanium oxides, are widely used because of their remarkable enhancement of the mechanical, electrical, barrier, and flame-retardancy properties of organic polymers. The dispersion and size of the fillers determine the performance of nanocomposites and, despite numerous methods and processing conditions reported in the literature, a universally simple method to scale up the distribution of nanofillers remains a challenge. A significant part of our research involves formulation of novel nanodielectrics that can withstand high electric fields and exhibit superior mechanical performance. Focusing on nanocomposites operating at cryogenic temperatures, our group developed an in situ method for nucleating titanium dioxide (TiO{sub 2}) nanoparticles in polyvinyl alcohol. We also applied this method to a variety of polymer matrices. Here, we present our recent work on a cryogenic resin filled with TiO{sub 2} nanoparticles. Using a particle-precursor solution from which TiO{sub 2} precipitates, we nucleated nanoparticles within the cryogenic epoxy resin Araldite 5808 (Huntsman Advanced Materials Inc., USA). We fabricated nanocomposite films at low weight percentages ({approx}2.5%) to avoid formation of large aggregates and interfaces. The morphology and dispersion of the in situ synthesized nanoparticles are shown by low- and high-magnification transmission-electron-microscopy (TEM) images. The TiO{sub 2} particles ({le}5nm in diameter) are uniformly nucleated and form evenly distributed nanometer-sized clusters in the polymer matrix. This morphology differs significantly from nanocomposites

  3. JPL Carbon Dioxide Laser Absorption Spectrometer Data Processing Results for the 2010 Flight Campaign

    NASA Technical Reports Server (NTRS)

    Jacob, Joseph C.; Spiers, Gary D.; Menzie, Robert T.; Christensen, Lance E.

    2011-01-01

    As a precursor to and validation of the core technology necessary for NASA's Active Sensing of CO2 Emissions over Nights, Days,and Seasons (ASCENDS) mission, we flew JPL's Carbon Dioxide Laser Absorption Spectrometer (CO2LAS) in a campaign of five flights onboard NASA's DC-8 Airborne Laboratory in July 2010. This is the latest in a series of annual flight campaigns that began in 2006, and our first on the DC-8 aircraft.

  4. A hybrid absorption–adsorption method to efficiently capture carbon

    PubMed Central

    Liu, Huang; Liu, Bei; Lin, Li-Chiang; Chen, Guangjin; Wu, Yuqing; Wang, Jin; Gao, Xueteng; Lv, Yining; Pan, Yong; Zhang, Xiaoxin; Zhang, Xianren; Yang, Lanying; Sun, Changyu; Smit, Berend; Wang, Wenchuan

    2014-01-01

    Removal of carbon dioxide is an essential step in many energy-related processes. Here we report a novel slurry concept that combines specific advantages of metal-organic frameworks, ion liquids, amines and membranes by suspending zeolitic imidazolate framework-8 in glycol-2-methylimidazole solution. We show that this approach may give a more efficient technology to capture carbon dioxide compared to conventional technologies. The carbon dioxide sorption capacity of our slurry reaches 1.25 mol l−1 at 1 bar and the selectivity of carbon dioxide/hydrogen, carbon dioxide/nitrogen and carbon dioxide/methane achieves 951, 394 and 144, respectively. We demonstrate that the slurry can efficiently remove carbon dioxide from gas mixtures at normal pressure/temperature through breakthrough experiments. Most importantly, the sorption enthalpy is only −29 kJ mol−1, indicating that significantly less energy is required for sorbent regeneration. In addition, from a technological point of view, unlike solid adsorbents slurries can flow and be pumped. This allows us to use a continuous separation process with heat integration. PMID:25296559

  5. Crystal-Size Effects on Carbon Dioxide Capture of a Covalently Alkylamine-Tethered Metal-Organic Framework Constructed by a One-Step Self-Assembly

    PubMed Central

    Kim, Yun Kyeong; Hyun, Sung-min; Lee, Jae Hwa; Kim, Tae Kyung; Moon, Dohyun; Moon, Hoi Ri

    2016-01-01

    To enhance the carbon dioxide (CO2) uptake of metal-organic frameworks (MOFs), amine functionalization of their pore surfaces has been studied extensively. In general, amine-functionalized MOFs have been synthesized via post-synthetic modifications. Herein, we introduce a one-step construction of a MOF ([(NiLethylamine)(BPDC)] = MOFNH2; [NiLethylamine]2+ = [Ni(C12H32N8)]2+; BPDC2− = 4,4‘-biphenyldicarboxylate) possessing covalently tethered alkylamine groups without post-synthetic modification. Two-amine groups per metal centre were introduced by this method. MOFNH2 showed enhanced CO2 uptake at elevated temperatures, attributed to active chemical interactions between the amine groups and the CO2 molecules. Due to the narrow channels of MOFNH2, the accessibility to the channel of CO2 is the limiting factor in its sorption behaviour. In this context, only crystal size reduction of MOFNH2 led to much faster and greater CO2 uptake at low pressures. PMID:26757890

  6. Nonthermal processing of orange juice using a pilot-plant scale supercritical carbon dioxide system with a gas-liquid metal contactor

    Technology Transfer Automated Retrieval System (TEKTRAN)

    To evaluate the effect of pilot-plant scale, non-thermal supercritical carbon dioxide (SCCO2) processing on the safety and the quality of orange juice (OJ), SCCO2 processed juice was compared with untreated fresh juice and equivalently thermal processed juice in terms of lethality. SCCO2 processing ...

  7. Classical trajectory study of alignment effects in the capture process: He 2+-Li ∗(2pΣ,2pΠ) collisions

    NASA Astrophysics Data System (ADS)

    Perumal, A. N.; Tripathi, D. N.

    1998-08-01

    A simulation method (CTMC) has been used to investigate the selectivity and alignment effects on the capture process in He 2+-Li ∗(2pΣ,2pΠ) collisions. The anomalous results of the experiment (∼ 50% error) as well as the AO calculation of Gieler et al. in case of capture into He II ( n = 4) from the initial Li ∗ (2pΣ) state are not found in the present work. Relative velocity and spatial overlap together mainly control the capture process in ion-atom collisions. The n-distribution of the final capture state is also presented.

  8. Beyond Self-Report: Emerging Methods for Capturing Individual Differences in Decision-Making Process

    PubMed Central

    Connors, Brenda L.; Rende, Richard; Colton, Timothy J.

    2016-01-01

    People vary in the way in which they approach decision-making, which impacts real-world behavior. There has been a surge of interest in moving beyond reliance on self-report measures to capture such individual differences. Particular emphasis has been placed on devising and applying a range of methodologies that include experimental, neuroscience, and observational paradigms. This paper provides a selective review of recent studies that illustrate the methods and yield of these approaches in terms of generating a deeper understanding of decision-making style and the notable differences that can be found across individuals. PMID:26973589

  9. Beneficial Use of Carbon Dioxide in Precast Concrete Production

    SciTech Connect

    Shao, Yixin

    2014-06-26

    The feasibility of using carbon dioxide as feedstock in precast concrete production is studied. Carbon dioxide reacts with calcium compounds in concrete, producing solid calcium carbonates in binding matrix. Two typical precast products are examined for their capacity to store carbon dioxide during the production. They are concrete blocks and fiber-cement panels. The two products are currently mass produced and cured by steam. Carbon dioxide can be used to replace steam in curing process to accelerate early strength, improve the long-term durability and reduce energy and emission. For a reaction within a 24-hour process window, the theoretical maximum possible carbon uptake in concrete is found to be 29% based on cement mass in the product. To reach the maximum uptake, a special process is developed to promote the reaction efficiency to 60-80% in 4-hour carbon dioxide curing and improve the resistance to freeze-thaw cycling and sulfate ion attack. The process is also optimized to meet the project target of $10/tCO2 in carbon utilization. By the use of self-concentrating absorption technology, high purity CO2 can be produced at a price below $40/t. With low cost CO2 capture and utilization technologies, it is feasible to establish a network for carbon capture and utilization at the vicinity of carbon sources. If all block produces and panel producers in United States could adopt carbon dioxide process in their production in place of steam, carbon utilization in these two markets alone could consume more than 2 Mt CO2/year. This capture and utilization process can be extended to more precast products and will continue for years to come.

  10. Tuning Organic Carbon Dioxide Absorbents for Carbonation and Decarbonation

    PubMed Central

    Rajamanickam, Ramachandran; Kim, Hyungsoo; Park, Ji-Woong

    2015-01-01

    The reaction of carbon dioxide with a mixture of a superbase and alcohol affords a superbase alkylcarbonate salt via a process that can be reversed at elevated temperatures. To utilize the unique chemistry of superbases for carbon capture technology, it is essential to facilitate carbonation and decarbonation at desired temperatures in an easily controllable manner. Here, we demonstrate that the thermal stabilities of the alkylcarbonate salts of superbases in organic solutions can be tuned by adjusting the compositions of hydroxylic solvent and polar aprotic solvent mixtures, thereby enabling the best possible performances to be obtained from the various carbon dioxide capture agents based on these materials. The findings provides valuable insights into the design and optimization of organic carbon dioxide absorbents. PMID:26033537

  11. A Comparison of Carbon Dioxide Sources for Mosquito Capture in Centers for Disease Control and Prevention Light Traps on the Florida Gulf Coast (1).

    PubMed

    Hoel, David F; Dunford, James C; Kline, Daniel L; Irish, Seth R; Weber, Michael; Richardson, Alec G; Doud, Carl W; Wirtz, Robert A

    2015-09-01

    Traditional sources of carbon dioxide (CO₂), dry ice, and compressed gas, were tested against 3 combinations of food-grade reagents known to generate CO₂using a compact, lightweight generator delivery system with Centers for Disease Control and Prevention light traps. Three 6 × 6 Latin square trials were completed near the Florida Gulf Coast in the Lower Suwannee Wildlife Refuge during the summer of 2013, collecting a total of 31,632 female mosquitoes. Treatments included dry ice, compressed CO₂gas, a control trap (no CO₂), citric acid + sodium bicarbonate, vinegar + sodium bicarbonate, and yeast + sugar. Decreasing order of trap collections (treatment mean number of mosquitoes per trap night ± standard error) were dry ice 773.5 (± 110.1) > compressed gas 440.7 (± 42.3) > citric acid + sodium bicarbonate 197.6 (± 30.4), yeast + sugar 153.6 (± 27.4) > vinegar + sodium bicarbonate 109.6 (± 16.2) > control 82.4 (± 14.0). A 2-way Kruskal-Wallis analysis by treatment, site, and treatment × site interaction identified significant differences between all treatments. Although dry ice and compressed CO₂gas collected significantly more mosquitoes than other combinations (P < 0.05), use of citric acid and sodium bicarbonate or yeast and sugar greatly outperformed unbaited traps and offer a good alternative to dry ice and compressed gas in areas where these agents are not readily available or are difficult to obtain due to logistical constraints. An inexpensive, portable CO₂generator for use with food-grade reagents is described.

  12. A Comparison of Carbon Dioxide Sources for Mosquito Capture in Centers for Disease Control and Prevention Light Traps on the Florida Gulf Coast (1).

    PubMed

    Hoel, David F; Dunford, James C; Kline, Daniel L; Irish, Seth R; Weber, Michael; Richardson, Alec G; Doud, Carl W; Wirtz, Robert A

    2015-09-01

    Traditional sources of carbon dioxide (CO₂), dry ice, and compressed gas, were tested against 3 combinations of food-grade reagents known to generate CO₂using a compact, lightweight generator delivery system with Centers for Disease Control and Prevention light traps. Three 6 × 6 Latin square trials were completed near the Florida Gulf Coast in the Lower Suwannee Wildlife Refuge during the summer of 2013, collecting a total of 31,632 female mosquitoes. Treatments included dry ice, compressed CO₂gas, a control trap (no CO₂), citric acid + sodium bicarbonate, vinegar + sodium bicarbonate, and yeast + sugar. Decreasing order of trap collections (treatment mean number of mosquitoes per trap night ± standard error) were dry ice 773.5 (± 110.1) > compressed gas 440.7 (± 42.3) > citric acid + sodium bicarbonate 197.6 (± 30.4), yeast + sugar 153.6 (± 27.4) > vinegar + sodium bicarbonate 109.6 (± 16.2) > control 82.4 (± 14.0). A 2-way Kruskal-Wallis analysis by treatment, site, and treatment × site interaction identified significant differences between all treatments. Although dry ice and compressed CO₂gas collected significantly more mosquitoes than other combinations (P < 0.05), use of citric acid and sodium bicarbonate or yeast and sugar greatly outperformed unbaited traps and offer a good alternative to dry ice and compressed gas in areas where these agents are not readily available or are difficult to obtain due to logistical constraints. An inexpensive, portable CO₂generator for use with food-grade reagents is described. PMID:26375906

  13. Outstanding field emission properties of wet-processed titanium dioxide coated carbon nanotube based field emission devices

    SciTech Connect

    Xu, Jinzhuo; Ou-Yang, Wei Chen, Xiaohong; Guo, Pingsheng; Piao, Xianqing; Sun, Zhuo; Xu, Peng; Wang, Miao; Li, Jun

    2015-02-16

    Field emission devices using a wet-processed composite cathode of carbon nanotube films coated with titanium dioxide exhibit outstanding field emission characteristics, including ultralow turn on field of 0.383 V μm{sup −1} and threshold field of 0.657 V μm{sup −1} corresponding with a very high field enhancement factor of 20 000, exceptional current stability, and excellent emission uniformity. The improved field emission properties are attributed to the enhanced edge effect simultaneously with the reduced screening effect, and the lowered work function of the composite cathode. In addition, the highly stable electron emission is found due to the presence of titanium dioxide nanoparticles on the carbon nanotubes, which prohibits the cathode from the influence of ions and free radical created in the emission process as well as residual oxygen gas in the device. The high-performance solution-processed composite cathode demonstrates great potential application in vacuum electronic devices.

  14. Reactions for improving efficiencies in thermochemical cycles related to the sulfur dioxide-iodine process

    SciTech Connect

    Mason, C.F.V.; Bowman, M.G.

    1982-01-01

    A modification of the sulfur dioxide-iodine cycle which uses magnesium oxide, magnesium sulfite and magnesium iodide is examined with particular emphasis on decreasing the amount of water employed and thereby increasing the efficiency. The key reaction is that of iodine with magnesium oxide and magnesium sulfite hexahydrate with no additional water. This produces 77% of the total possible sulfate as well as magnesium iodide, hydrogen iodide and hydrogen at 523/sup 0/K. The efficiency of this cycle varies between 58% and 39% depending on the amount of heat that can be recovered. This is the first example of a cycle where there is no large energy burden due to evaporation.

  15. Progress and new developments in carbon capture and storage

    SciTech Connect

    Plasynski, S.I.; Litynski, J.T.; McIlvried, H.G.; Srivastava, R.D.

    2009-07-01

    Growing concern over the impact on global climate change of the buildup of greenhouse gases (GHGs) in the atmosphere has resulted in proposals to capture carbon dioxide (CO{sub 2}) at large point sources and store it in geologic formations, such as oil and gas reservoirs, unmineable coal seams, and saline formations, referred to as carbon capture and storage (CCS). There are three options for capturing CO{sub 2} from point sources: post-combustion capture, pre-combustion capture, and oxy-combustion. Several processes are available to capture CO{sub 2}, and new or improved processes are under development. However, CO{sub 2} capture is the most expensive part of CCS, typically accounting for 75% of overall cost. CCS will benefit significantly from the development of a lower cost post-combustion CO{sub 2} capture process that can be retrofitted to existing power plants. Once captured, the CO{sub 2} is compressed to about 150 atm and pipelined at supercritical conditions to a suitable storage site. Oil and gas reservoirs, because they have assured seals and are well characterized, are promising early opportunity sites. Saline formations are much more extensive and have a huge potential storage capacity, but are much less characterized. Several commercial and a number of pilot CCS projects are underway around the world.

  16. The carbon dioxide cycle

    USGS Publications Warehouse

    James, P.B.; Hansen, G.B.; Titus, T.N.

    2005-01-01

    The seasonal CO2 cycle on Mars refers to the exchange of carbon dioxide between dry ice in the seasonal polar caps and gaseous carbon dioxide in the atmosphere. This review focuses on breakthroughs in understanding the process involving seasonal carbon dioxide phase changes that have occurred as a result of observations by Mars Global Surveyor. ?? 2004 COSPAR. Published by Elsevier Ltd. All rights reserved.

  17. Combined Extraction Processes of Lipid from Chlorella vulgaris Microalgae: Microwave Prior to Supercritical Carbon Dioxide Extraction

    PubMed Central

    Dejoye, Céline; Vian, Maryline Abert; Lumia, Guy; Bouscarle, Christian; Charton, Frederic; Chemat, Farid

    2011-01-01

    Extraction yields and fatty acid profiles from freeze-dried Chlorella vulgaris by microwave pretreatment followed by supercritical carbon dioxide (MW-SCCO2) extraction were compared with those obtained by supercritical carbon dioxide extraction alone (SCCO2). Work performed with pressure range of 20–28 Mpa and temperature interval of 40–70 °C, gave the highest extraction yield (w/w dry weight) at 28 MPa/40 °C. MW-SCCO2 allowed to obtain the highest extraction yield (4.73%) compared to SCCO2 extraction alone (1.81%). Qualitative and quantitative analyses of microalgae oil showed that palmitic, oleic, linoleic and α-linolenic acid were the most abundant identified fatty acids. Oils obtained by MW-SCCO2 extraction had the highest concentrations of fatty acids compared to SCCO2 extraction without pretreatment. Native form, and microwave pretreated and untreated microalgae were observed by scanning electronic microscopy (SEM). SEM micrographs of pretreated microalgae present tearing wall agglomerates. After SCCO2, microwave pretreated microalgae presented several micro cracks; while native form microalgae wall was slightly damaged. PMID:22272135

  18. The capture and destruction of chlorinated solvents via electrokinetic pumping: The LASAGNA{trademark} process

    SciTech Connect

    Salvo, J.J.; Ho, S.V.; Shoemaker, S.H.

    1995-12-31

    Remediating soils and groundwater that have been contaminated with chlorinated solvents is a significant challenge for current environmental technology. Soils with a high proportion of fine silts and clays have been especially recalcitrant due to their low permeability. Recently, electrokinetics has shown great promise in gaining access to these contaminated zones that fail to yield with traditional pumping methods. An integrated approach using electrokinetics combined with in situ capture and destruction zones (LASAGNA{sup trademark}) is being developed and field tested by Monsanto, DuPont and GE under the auspices of the EPA`s Remediation Technology Development Forum and with financial support from the Department of Energy. To speed implementation and encourage partnering, royalty-free cross-licensing of the developed technology is available to consortium members for use on their sites.

  19. The theory and methodology of capturing and representing the design process and its application to the task of rapid redesign

    NASA Astrophysics Data System (ADS)

    Nii, Kendall M.

    The paradigm under which engineering design is being performed in the Aerospace industry is changing. There is an increased emphasis on a "faster, better, and cheaper" way of doing business. Designers are tasked with developing a better product, in a shorter time, with less money. Engineers are continually trying to improve their products, lower their costs, and reduce their schedules. So at first glance, it might seem difficult if not impossible to perform these three tasks simultaneously and attempt to achieve order of magnitude improvements in each area. Indeed it might well be impossible for an engineer using only traditional tools and techniques. However, there is a new tool, known as design capture, available to the designer. A design capture system, can aid the designer in a variety of ways. One specific use for a design capture system is to aid the designer in performing rapid redesign. This thesis presents a new methodology for a Design Capture System (DCS) which can aid the designer with performing rapid redesign. The Design Capture for Rapid Redesign (DCARRD) method facilitates rapid redesign in three ways: it allows the designer to assess the impact of changing an initial requirement, it allows the designer to assess the impact of changing a decision, and it enhances the ability of the designer to assess the impact of a completely new requirement. The DCARRD method was implemented into an html-based design capture system accessible through a Web browser. This implementation demonstrates the feasibility of the DCARRD method. The most important features of DCARRD are that it is focused an performing rapid redesign, it places the design decisions within the framework of the design process, it is simple to use and implement, and it has the ability to track subsystem baselines. The many complex issues surrounding testing of design tools in general, and DCARRD in particular, are discussed at length. There are a number of complex issues which must be addressed

  20. Groundwater capture processes under a seasonal variation in natural recharge and discharge

    NASA Astrophysics Data System (ADS)

    Maddock, Thomas, III.; Vionnet, Leticia Beatriz

    "Capture" is the increase in recharge and the decrease in discharge that occurs when pumping is imposed on an aquifer system that was in a previous state of approximate dynamic equilibrium. Regional groundwater models are usually used to calculate capture in a two-step procedure. A steady-state solution provides an initial-head configuration, a set of flows through the boundaries for the modeled region, and the initial basis for the capture calculation. The transient solutions provide the total change in flows through the boundaries. A difference between the transient and steady-state solutions renders the capture calculation. When seasonality is a modeling issue, the use of a single initial hydraulic head and a single set of boundary flows leads to miscalculations of capture. Instead, an initial condition for each season should be used. This approach may be accomplished by determining steady oscillatory solutions, which vary through the seasons but repeat from year to year. A regional groundwater model previously developed for a portion of the San Pedro River basin, Arizona, USA, is modified to illustrate the effect that different initial conditions have on transient solutions and on capture calculations. Résumé Les "prélèvements" sont constitués par l'augmentation de la recharge et par la diminution de l'écoulement qui se produit lorsqu'un pompage est imposéà un système aquifère qui était auparavant dans un état proche de l'équilibre dynamique. Les modèles régionaux de nappe sont en général utilisés pour calculer les prélèvements dans une procédure à deux étapes. Une solution en régime permanent donne la configuration piézométrique initiale, un jeu de conditions aux limites pour la région modélisée et les données de base pour le calcul des prélèvements. Les solutions transitoires donnent les modifications globales des conditions aux limites. Lorsque des variations saisonnières sont produites en sortie du modèle, le recours à une

  1. Development of a Novel Gas Pressurized Stripping Process-Based Technology for CO₂ Capture from Post-Combustion Flue Gases

    SciTech Connect

    Chen, Shiaoguo

    2015-09-30

    A novel Gas Pressurized Stripping (GPS) post-combustion carbon capture (PCC) process has been developed by Carbon Capture Scientific, LLC, CONSOL Energy Inc., Nexant Inc., and Western Kentucky University in this bench-scale project. The GPS-based process presents a unique approach that uses a gas pressurized technology for CO₂ stripping at an elevated pressure to overcome the energy use and other disadvantages associated with the benchmark monoethanolamine (MEA) process. The project was aimed at performing laboratory- and bench-scale experiments to prove its technical feasibility and generate process engineering and scale-up data, and conducting a techno-economic analysis (TEA) to demonstrate its energy use and cost competitiveness over the MEA process. To meet project goals and objectives, a combination of experimental work, process simulation, and technical and economic analysis studies were applied. The project conducted individual unit lab-scale tests for major process components, including a first absorption column, a GPS column, a second absorption column, and a flasher. Computer simulations were carried out to study the GPS column behavior under different operating conditions, to optimize the column design and operation, and to optimize the GPS process for an existing and a new power plant. The vapor-liquid equilibrium data under high loading and high temperature for the selected amines were also measured. The thermal and oxidative stability of the selected solvents were also tested experimentally and presented. A bench-scale column-based unit capable of achieving at least 90% CO₂ capture from a nominal 500 SLPM coal-derived flue gas slipstream was designed and built. This integrated, continuous, skid-mounted GPS system was tested using real flue gas from a coal-fired boiler at the National Carbon Capture Center (NCCC). The technical challenges of the GPS technology in stability, corrosion, and foaming of selected solvents, and environmental, health and

  2. Electron capture and ionization processes in high-velocity Cn+ , C-Ar and Cn+ , C-He collisions

    NASA Astrophysics Data System (ADS)

    Labaigt, G.; Jorge, A.; Illescas, C.; Béroff, K.; Dubois, A.; Pons, B.; Chabot, M.

    2015-04-01

    Single-electron and double-electron capture as well as projectile single-ionization and multiple-ionization processes in 125 keV u-1 Cn+-He (n = 1-5) and Cn+-Ar (n=1,2,4) collisions have been studied experimentally and theoretically. Helium target single-ionization and double-ionization cross sections are also reported for Cn+-He (n = 1, 4) collisions in the 100-400 keV u-1 impact energy domain. These results are compared with predictions from the independent atom and electron (IAE) model developed for describing cluster-atom collisions. The ion/atom-atom probabilities required for the IAE simulations have been determined by classical trajectory Monte Carlo (CTMC) and semiclassical atomic orbital close coupling (SCAOCC) calculations for the Ar and He targets, respectively. For comparison, electron capture cross sections were also measured in C-He and C-Ar collisions. In general the agreement between experiment and IAE calculations has been found to be rather good, with the exception of double-electron capture leading to anionic Cn- species.

  3. Ultrafast vibrational spectroscopy (2D-IR) of CO2 in ionic liquids: Carbon capture from carbon dioxide's point of view

    NASA Astrophysics Data System (ADS)

    Brinzer, Thomas; Berquist, Eric J.; Ren, Zhe; Dutta, Samrat; Johnson, Clinton A.; Krisher, Cullen S.; Lambrecht, Daniel S.; Garrett-Roe, Sean

    2015-06-01

    The CO2ν3 asymmetric stretching mode is established as a vibrational chromophore for ultrafast two-dimensional infrared (2D-IR) spectroscopic studies of local structure and dynamics in ionic liquids, which are of interest for carbon capture applications. CO2 is dissolved in a series of 1-butyl-3-methylimidazolium-based ionic liquids ([C4C1im][X], where [X]- is the anion from the series hexafluorophosphate (PF 6- ), tetrafluoroborate (BF 4- ), bis-(trifluoromethyl)sulfonylimide (Tf2N-), triflate (TfO-), trifluoroacetate (TFA-), dicyanamide (DCA-), and thiocyanate (SCN-)). In the ionic liquids studied, the ν3 center frequency is sensitive to the local solvation environment and reports on the timescales for local structural relaxation. Density functional theory calculations predict charge transfer from the anion to the CO2 and from CO2 to the cation. The charge transfer drives geometrical distortion of CO2, which in turn changes the ν3 frequency. The observed structural relaxation timescales vary by up to an order of magnitude between ionic liquids. Shoulders in the 2D-IR spectra arise from anharmonic coupling of the ν2 and ν3 normal modes of CO2. Thermal fluctuations in the ν2 population stochastically modulate the ν3 frequency and generate dynamic cross-peaks. These timescales are attributed to the breakup of ion cages that create a well-defined local environment for CO2. The results suggest that the picosecond dynamics of CO2 are gated by local diffusion of anions and cations.

  4. Simultaneous recovery of zinc and manganese dioxide from household alkaline batteries through hydrometallurgical processing

    NASA Astrophysics Data System (ADS)

    de Souza, Cleusa Cristina Bueno Martha; Tenório, Jorge Alberto Soares

    This paper describes the leaching experiments and the electrowinning tests to recover Zn and Mn from spent household alkaline batteries. After the dismantling of the batteries, the black powder was analyzed and found to contain 21 wt.% Zn and 45%wt. Mn. Therefore, it was considered that recovery of these metals would be interesting due to their relatively large amounts in this kind of waste. Batch laboratory experiments were carried out to develop an acid leaching procedure and to determine appropriate leaching conditions to maximize zinc extraction and to study the leaching behavior of Mn. An experimental study was undertaken to evaluate the feasibility of simultaneous recovery of zinc and particulate manganese dioxide using a laboratory cell. The results from these electrowinning experiments are also presented in this paper.

  5. Novel polymer membrane process for pre-combustion CO{sub 2} capture from coal-fired syngas

    SciTech Connect

    Merkel, Tim

    2011-09-14

    This final report describes work conducted for the Department of Energy (DOE NETL) on development of a novel polymer membrane process for pre-combustion CO{sub 2} capture from coalfired syngas (award number DE-FE0001124). The work was conducted by Membrane Technology and Research, Inc. (MTR) from September 15, 2009, through December 14, 2011. Tetramer Technologies, LLC (Tetramer) was our subcontract partner on this project. The National Carbon Capture Center (NCCC) at Wilsonville, AL, provided access to syngas gasifier test facilities. The main objective of this project was to develop a cost-effective membrane process that could be used in the relatively near-term to capture CO{sub 2} from shifted syngas generated by a coal-fired Integrated Gasification Combined Cycle (IGCC) power plant. In this project, novel polymeric membranes (designated as Proteus™ membranes) with separation properties superior to conventional polymeric membranes were developed. Hydrogen permeance of up to 800 gpu and H{sub 2}/CO{sub 2} selectivity of >12 was achieved using a simulated syngas mixture at 150°C and 50 psig, which exceeds the original project targets of 200 gpu for hydrogen permeance and 10 for H{sub 2}/CO{sub 2} selectivity. Lab-scale Proteus membrane modules (with a membrane area of 0.13 m{sup 2}) were also developed using scaled-up Proteus membranes and high temperature stable module components identified during this project. A mixed-gas hydrogen permeance of about 160 gpu and H{sub 2}/CO{sub 2} selectivity of >12 was achieved using a simulated syngas mixture at 150°C and 100 psig. We believe that a significant improvement in the membrane and module performance is likely with additional development work. Both Proteus membranes and lab-scale Proteus membrane modules were further evaluated using coal-derived syngas streams at the National Carbon Capture Center (NCCC). The results indicate that all module components, including the Proteus membrane, were stable under the field

  6. Effect of fossil fuels on the parameters of CO2 capture.

    PubMed

    Nagy, Tibor; Mizsey, Peter

    2013-08-01

    The carbon dioxide capture is a more and more important issue in the design and operation of boilers and/or power stations because of increasing environmental considerations. Such processes, absorber desorber should be able to cope with flue gases from the use of different fossil primary energy sources, in order to guarantee a flexible, stable, and secure energy supply operation. The changing flue gases have significant influence on the optimal operation of the capture process, that is, where the required heating of the desorber is the minimal. Therefore special considerations are devoted to the proper design and control of such boiler and/or power stations equipped with CO2 capture process.

  7. Low cost and compact analytical microsystem for carbon dioxide determination in production processes of wine and beer.

    PubMed

    Calvo-López, Antonio; Ymbern, Oriol; Izquierdo, David; Alonso-Chamarro, Julián

    2016-08-10

    The design, construction and evaluation of a low cost, cyclic olefin copolymer (COC)-based continuous flow microanalyzer, with optical detection, to monitor carbon dioxide in bottled wines and beers as well as in fermentation processes, is presented. The microsystem, constructed by computer numerically controlled (CNC) micromilling and using a multilayer approach, integrates microfluidics, gas-diffusion module and an optical flow-cell in a single polymeric substrate. Its size is slightly bigger than a credit card, exactly 45 × 60 × 4 mm in the microfluidic and diffusion module zone and 22.5 × 40 × 3 mm in the flow-cell zone. The gas-diffusion module is based on a hydrophobic polyvinylidene fluoride (PVDF) membrane, which allows the transfer of the carbon dioxide present in the sample to a bromothymol blue (BTB) pH-sensitive acceptor solution, where the color change is measured optically. The detection system consisted of a LED with an emission peak at 607 nm and a photodiode integrated in a printed circuit board (PCB). The obtained analytical features after the optimization of the microfluidic platform and hydrodynamic variables are a linear range from 255 to 10000 mg L(-1) of CO2 and a detection limit of 83 mg L(-1) with a sampling rate of 30 samples h(-1). PMID:27282752

  8. Hybrid Solvent-Membrane CO2 Capture: A Solvent/Membrane Hybrid Post-combustion CO2 Capture Process for Existing Coal-Fired Power Plants

    SciTech Connect

    2010-07-01

    IMPACCT Project: The University of Kentucky is developing a hybrid approach to capturing CO2 from the exhaust gas of coal-fired power plants. In the first, CO2 is removed as flue gas is passed through an aqueous ammonium-based solvent. In the second, carbon-rich solution from the CO2 absorber is passed through a membrane that is designed to selectively transport the bound carbon, enhancing its concentration on the permeate side. The team’s approach would combine the best of both membrane- and solventbased carbon capture technologies. Under the ARPA-E award, the team is enabling the membrane operation to be a drop-in solution.

  9. Neutron-capture nucleosynthesis of neodymium isotopes and the s-process from A = 130 to 150

    SciTech Connect

    Mathews, G.J.; Kaeppeler, F.

    1984-11-15

    New measurements of neutron capture cross sections for /sup 142,143,144/Nd are reported. These are combined with other recent measurements and applied to a detailed study of the s-proccess and r-process systematics for A = 130-150 nuclei. The influence of these results on the interpretation of isotopic anomalies observed in acid-insoluble residues and inclusions from the Allende meteorite is also examined. The uncertainties in the s-process sigmaN curve are significantly diminished in the present work, and a fit is obtained which is consistent with all of the s-process-only isotopes in this region. A somewhat larger value than previous determinations is obtained for the mean neutron exposure for heavy nuclei in the s-process, tau/sub 0/ = 0.29-0.35 mb/sup -1/. The derived r-process abundances decrease systematically from the A = 130 peak but exhibit a pronounced odd-even effect. The new results tend to confirm the hypothesis that the isotopic anomalies in materials from the Allende meteorite are the result of an unusual mixture of average solar-system s-process and r-process material, but an odd-even effect may be present in the r-process anomalies of inclusion EK1-4-1.

  10. The Helium r-Process and Neutron-Capture Element Abundances in Low Metallicity Stars

    NASA Astrophysics Data System (ADS)

    Truran, J. W.; Cowan, J. J.

    2000-05-01

    There is increasingly strong observational evidence that the r-process isotopes identified in solar system matter are in fact the products of two distinct classes of r-process nucleosynthesis events. Spectroscopic observations of extremely metal deficient halo field stars and globular cluster stars provide confirmation of the occurrence of a robust r-process mechanism for the production of the main r-process component, at mass numbers A ≳ 130-140. This main component is variously argued to have its origin in regions outside the neutronized core, in magnetic jets from the collapsing core, or in neutron star-neutron star mergers. The stellar abundance data available to date suggests, however, that the bulk of the r-process nuclei in the mass region A < ~ 130 are not formed in this environment. Further evidence for such a distinct weak component is provided by the finding that the abundances of the short lived r-process nuclei 129I and 182Hf in the early solar system cannot be explained by a single type of r-process event (Wasserburg, Busso, & Gallino 1996). We report here exploratory calculations of the consequences of r-process synthesis in the shock-processed helium shells of Type II supernovae. The conditions of temperature, density, and composition are those predicted by the models of Woosley and Weaver (1995). Our results establish that these conditions are quite consistent with the production of an r-process pattern of abundances for the A < ~ 130 mass region, although the sensitivity to detailed post shock conditions insures that this process is not as robust as that responsible for the main r-process component A ≳ 130-140. We discuss the implications of our numerical results for the interpretation both of the abundances in metal poor stars and of the anomalous r-process-like isotopic abundances observed in meteoritic silicon carbide grains (Pellin et al. 2000). This research was funded in part by NSF grant AST-9618332 to JJC and by the ASCI

  11. Synthesis, fractionation, and thin film processing of nanoparticles using the tunable solvent properties of carbon dioxide gas expanded liquids

    NASA Astrophysics Data System (ADS)

    Anand, Madhu

    nanoparticle populations. This study details the influence of various factors on the size separation process, such as the types of nanoparticles, ligand type and solvent type as well as the use of recursive fractionation and the time allowed for settling during each fractionation step. This size selective precipitation technique was also applied to fractionate and separate polydisperse dispersions of CdSe/ZnS semiconductor nanocrystals into very distinct size and color fractions based solely on the pressure tunable solvent properties of CO2 expanded liquids. This size selective precipitation of nanoparticles is achieved by finely tuning the solvent strength of the CO2/organic solvent medium by simply adjusting the applied CO2 pressure. These subtle changes affect the balance between osmotic repulsive and van der Waals attractive forces thereby allowing fractionation of the nanocrystals into multiple narrow size populations. Thermodynamic analysis of nanoparticle size selective fractionation was performed to develop a theoretical model based on the thermodynamic properties of gas expanded liquids. We have used the general phenomenon of nanoparticle precipitation with CO2 expanded liquids to create dodecanethiol stabilized gold nanoparticle thin films. This method utilizes CO2 as an anti-solvent for low defect, wide area gold nanoparticle film formation employing monodisperse gold nanoparticles. Dodecanethiol stabilized gold particles are precipitated from hexane by controllably expanding the solution with carbon dioxide. Subsequent addition of carbon dioxide as a dense supercritical fluid then provides for removal of the organic solvent while avoiding the dewetting effects common to evaporating solvents. Unfortunately, the use of carbon dioxide as a neat solvent in nanoparticles synthesis and processing is limited by the very poor solvent strength of dense phase CO2. As a result, most current techniques employed to synthesize and disperse nanoparticles in neat carbon dioxide

  12. Impact of the uncertainty in α-captures on 22Ne on the weak s-process in massive stars

    NASA Astrophysics Data System (ADS)

    Nishimura, N.; Hirschi, R.; Pignatari, M.; Herwig, F.; Beard, M.; Imbriani, G.; Görres, J.; deBoer, R. J.; Wiescher, M.

    2014-05-01

    Massive stars at solar metallicity contribute to the production of heavy elements with atomic masses between A = 60 and A = 90 via the so-called weak s-process (which takes place during core He and shell C burning phases). Furthermore, recent studies have shown that rotation boosts the s-process production in massive stars at low metallicities, with a production that may reach the barium neutron-magic peak. These results are very sensitive to neutron source and neutron poison reaction rates. For the weak s-process, the main neutron source is the reaction 22Ne(α,n)25Mg, which is in competition with 22Ne(α,γ)26Mg. The uncertainty of both rates strongly affects the nucleosynthesis predictions from stellar model calculations. In this study, we investigate the impact of the uncertainty in α-captures on 22Ne on the s-process nucleosynthesis in massive stars both at solar and at very low metallicity. For this purpose, we post-process, with the Nugrid mppnp code, non-rotating and rotating evolutionary models 25M⊙ stars at two different metallicities: Z = Z⊙ and Z = 10-5Z⊙, respectively. Our results show that uncertainty of 22Ne(α,n)25Mg and 22Ne(α,γ)26Mg rates have a significant impact on the final elemental production especially for metal poor rotating models. Beside uncertainties in the neutron source reactions, for fast rotating massive stars at low metallicity we revisit the impact of the neutron poisoning effect by the reaction chain 16O(n,γ)17O(α,γ)21Ne, in competition with the 17O(α,n)20Ne, recycling the neutrons captured by 16O.

  13. The search for the site of the r-process. [rapid neutron capture in stellar nucleosynthesis

    NASA Technical Reports Server (NTRS)

    Cowan, John J.; Cameron, A. G. W.; Truran, J. W.; Sneden, Christopher

    1986-01-01

    A number of sites have been suggested for the r-process, including neutronized cores of exploding supernovae, jets of neutronized matter ejected from the collapse of rotating magnetized stellar cores, the helium and carbon zones of stars undergoing supernova explosions, and helium core flashes in low-mass stars. Despite much work and many advances in nuclear physics, the site or sites of the r-process is still unknown. Observations of metal-poor stars in the halo of the Galaxy indicate r-process production early in the history of the Galaxy and provide important constraints on galactic nucleosynthesis. Further observations of metal-poor stars, along with advances in understanding the nuclear properties of neutron-rich nuclei and improved astrophysical models of stars in the late stages of evolution, should help to identify the site of the r-process.

  14. Penetrator reliability investigation and design exploration : from conventional design processes to innovative uncertainty-capturing algorithms.

    SciTech Connect

    Martinez-Canales, Monica L.; Heaphy, Robert; Gramacy, Robert B.; Taddy, Matt; Chiesa, Michael L.; Thomas, Stephen W.; Swiler, Laura Painton; Hough, Patricia Diane; Lee, Herbert K. H.; Trucano, Timothy Guy; Gray, Genetha Anne

    2006-11-01

    This project focused on research and algorithmic development in optimization under uncertainty (OUU) problems driven by earth penetrator (EP) designs. While taking into account uncertainty, we addressed three challenges in current simulation-based engineering design and analysis processes. The first challenge required leveraging small local samples, already constructed by optimization algorithms, to build effective surrogate models. We used Gaussian Process (GP) models to construct these surrogates. We developed two OUU algorithms using 'local' GPs (OUU-LGP) and one OUU algorithm using 'global' GPs (OUU-GGP) that appear competitive or better than current methods. The second challenge was to develop a methodical design process based on multi-resolution, multi-fidelity models. We developed a Multi-Fidelity Bayesian Auto-regressive process (MF-BAP). The third challenge involved the development of tools that are computational feasible and accessible. We created MATLAB{reg_sign} and initial DAKOTA implementations of our algorithms.

  15. Production of Very Pure Hydrogen with Simultaneous Capture of Carbon Dioxide using the Redox Reactions of Iron Oxides in Packed Beds

    SciTech Connect

    Bohn, C.D.; Muller, C.R.; Cleeton, J.P.; Hayhurst, A.N.; Davidson,J.F.; Scott, S.A.; Dennis, J.S.

    2008-10-15

    A chemical looping process, which uses a packed bed of the various oxides of iron, has been formulated to produce separate, pure streams of H{sub 2} and CO{sub 2} from syngas. The process has the following stages: (1) Reduction of Fe{sub 2}O{sub 3} to Fe{sub 0.947}O in the syngas from gasifying coal or biomass. This stage generates pure CO{sub 2}, once the water has been condensed. (2) Subsequent oxidation of Fe{sub 0.947}O to Fe3O{sub 4} using stearn, to simultaneously produce H{sub 2}. (3) Further oxidation of Fe3O{sub 4} to Fe{sub 2}O{sub 3} using air to return the oxide to step 1. Step 1 was studied here using a Mixture of CO + CO{sub 2} + N{sub 2} as the feed to a packed bed of iron oxide particles, while measuring the concentrations of CO and CO{sub 2} in the off-gas; step 2 was investigated by passing steam in N{sub 2} through the packed bed and measuring the quantity of H{sub 2} produced. The third step simply involved passing air through the bed. Reduction to Fe, rather than Fe{sub 0.947}O, in step 1 gave low levels of H{sub 2} in step 2 after 10 cycles of reduction and oxidation and led to the deposition of carbon at lower temperature. Step 3, i.e. reoxidizing the particles in air to Fe{sub 2}O{sub 3}, led to no deterioration of the hydrogen yield in step 2 and benefited the process by (I) increasing the heat produced in each redox cycle and (ii) preventing the slip of CO from the bed in step 1. The proposed process is exothermic overall and very usefully generates separate streams of very pure H{sub 2} and CO, without complicated separation units.

  16. Ionization of water by (20-150)-keV protons: Separation of direct-ionization and electron-capture processes

    SciTech Connect

    Gobet, F.; Eden, S.; Coupier, B.; Tabet, J.; Farizon, B.; Farizon, M.; Gaillard, M.J.; Carre, M.; Ouaskit, S.; Maerk, T. D.; Scheier, P.

    2004-12-01

    Mass analyzed product ions have been detected in coincidence with the projectile following the ionization of water by proton impact. Measurement of the projectile charge state postcollision enables the different ionization processes to be identified: direct ionization, single electron capture, and double electron capture. A complete set of partial and total absolute cross sections is reported for the direct ionization and electron capture processes initiated by proton collisions at 20-150 keV. The cross sections for the direct ionization of H{sub 2}O by proton impact are compared with previous electron impact results [Straub et al., J. Chem. Phys. 108, 109 (1998)].

  17. Neutron capture reactions relevant to the s and p processes in the region of the N =50 shell closure

    NASA Astrophysics Data System (ADS)

    Dutta, Saumi; Gangopadhyay, G.; Bhattacharyya, Abhijit

    2016-08-01

    The radiative neutron capture cross sections for nuclei participating in the s -process and the p -process nucleosynthesis in and around the N =50 closed neutron shell have been calculated in a statistical semimicroscopic Hauser-Feshbach approach for the energy range of astrophysical interest. A folded optical-model potential is constructed utilizing the standard DDM3Y real nucleon-nucleon interaction. The folding of the interaction with target radial matter densities, obtained from the relativistic mean-field theory, is done in coordinate space using the spherical approximation. The standard nuclear reaction code talys1.8 is used for cross-section calculation. The cross sections are compared with experimental results. Maxwellian-averaged cross sections and astrophysical reaction rates for a number of selected nuclei are also presented.

  18. Synthesization of Nanostructured Titanium Dioxide at Low Molarity of Sol-Gel Process

    NASA Astrophysics Data System (ADS)

    Maarof, S. K. M.; Abdullah, S.; Rusop, M.

    2013-06-01

    Titanium dioxide, TiO2 is one of the semiconductor materials. The aim of this paper is to determine the production of TiO2 by sol-gel method. The sol-gel method used because this method is quite simple compare to other methods such as dip-coated and refractive sputtering. The parameter will be used in this paper is the concentration. The sol-gel TiO2 solution then spin coated on the glass substrate to form homogenous and transparent thin film. The thin film was coated at 8 layers to adjust the refractive index characteristics and to get the clear images during characterize by spin coating technique. Other than that, this work also to get the band gap energy similar to the standard bandgap for TiO2. The optical properties such as absorption and transmittance of TiO2 can be done by Ultraviolet-visible Spectroscopy (UV-Vis). The changes on the surface morphology were observed using Atomic Force Microscopy (AFM), Field Emission Scanning Electron Microscopy (FESEM). Based on the result, higher the molarity of TiO2, the uniformity of the surface morphology, and the energy bandgap is much better. Higher the molarity, the bandgap will be lower with 0.1M (3.78 eV) and its too large compare to the standard value (3.2 eV).

  19. A comparison of iodinated trihalomethane formation from chlorine, chlorine dioxide and potassium permanganate oxidation processes.

    PubMed

    Zhang, Tian-Yang; Xu, Bin; Hu, Chen-Yan; Lin, Yi-Li; Lin, Lin; Ye, Tao; Tian, Fu-Xiang

    2015-01-01

    This study compared the formation of iodinated trihalomethanes (I-THMs) from iodide-containing raw waters oxidized by chlorine, chlorine dioxide (ClO₂) and potassium permanganate (KMnO₄) at different oxidant concentrations, reaction times, pHs, initial iodide concentrations and bromide to iodide mass ratios. Among the six investigated I-THMs, iodoform was the major species formed during the oxidation using chlorine, ClO₂ and KMnO₄. When oxidant concentration increased from 0.1 to 3.0 mg/L, the formation of I-THMs increased and then decreased for chlorine and ClO₂, but kept increasing for KMnO₄. As the reaction time went by, I-THM concentration increased to a plateau within 10 h (ClO₂ within only 1 h, especially) for all the three oxidants. I-THM formation gradually increased from pH 3.0 to 9.0 and remained stable at pH values higher than 7.5 for chlorine; however, for ClO₂ and KMnO₄ the highest I-THM formation showed at pH 7.0 and 7.5, respectively. As initial iodide concentration increased from 20 to 800 μg/L, the total amount and species of I-THMs increased for the three oxidants. Iodide contributed to I-THM formation much more significantly than bromide.

  20. Supercritical Carbon Dioxide Extraction of Bioactive Compounds from Ampelopsis grossedentata Stems: Process Optimization and Antioxidant Activity

    PubMed Central

    Wang, Yuefei; Ying, Le; Sun, Da; Zhang, Shikang; Zhu, Yuejin; Xu, Ping

    2011-01-01

    Supercritical carbon dioxide (SC-CO2) extraction of bioactive compounds including flavonoids and phenolics from Ampelopsis grossedentata stems was carried out. Extraction parameters such as pressure, temperature, dynamic time and modifier, were optimized using an orthogonal array design of L9 (34), and antioxidant activities of the extracts were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay and ferrous ion chelating (FIC) assay. The best conditions obtained for SC-CO2 extraction of flavonoids was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:3, v/v), and that for phenolics extraction was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:1, v/v). Meantime, flavonoids and phenolics were found to be mainly responsible for the DPPH scavenging activity of the extracts, but not for the chelating activity on ferrous ion according to Pearson correlation analysis. Furthermore, several unreported flavonoids such as apigenin, vitexin, luteolin, etc., have been detected in the extracts from A. grossedentata stems. PMID:22072923

  1. Investigation of model capability in capturing vertical hydrodynamic coastal processes: a case study in the north Adriatic Sea

    NASA Astrophysics Data System (ADS)

    McKiver, W. J.; Sannino, G.; Braga, F.; Bellafiore, D.

    2016-01-01

    In this work we consider a numerical study of hydrodynamics in the coastal zone using two different models, SHYFEM (shallow water hydrodynamic finite element model) and MITgcm (Massachusetts Institute of Technology general circulation model), to assess their capability to capture the main processes. We focus on the north Adriatic Sea during a strong dense water event that occurred at the beginning of 2012. This serves as an interesting test case to examine both the models strengths and weaknesses, while giving an opportunity to understand how these events affect coastal processes, like upwelling and downwelling, and how they interact with estuarine dynamics. Using the models we examine the impact of setup, surface and lateral boundary treatment, resolution and mixing schemes, as well as assessing the importance of nonhydrostatic dynamics in coastal processes. Both models are able to capture the dense water event, though each displays biases in different regions. The models show large differences in the reproduction of surface patterns, identifying the choice of suitable bulk formulas as a central point for the correct simulation of the thermohaline structure of the coastal zone. Moreover, the different approaches in treating lateral freshwater sources affect the vertical coastal stratification. The results indicate the importance of having high horizontal resolution in the coastal zone, specifically in close proximity to river inputs, in order to reproduce the effect of the complex coastal morphology on the hydrodynamics. A lower resolution offshore is acceptable for the reproduction of the dense water event, even if specific vortical structures are missed. Finally, it is found that nonhydrostatic processes are of little importance for the reproduction of dense water formation in the shelf of the north Adriatic Sea.

  2. An overview of biological processes and their potential for CO2 capture.

    PubMed

    Goli, Amin; Shamiri, Ahmad; Talaiekhozani, Amirreza; Eshtiaghi, Nicky; Aghamohammadi, Nasrin; Aroua, Mohamed Kheireddine

    2016-12-01

    The extensive amount of available information on global warming suggests that this issue has become prevalent worldwide. Majority of countries have issued laws and policies in response to this concern by requiring their industrial sectors to reduce greenhouse gas emissions, such as CO2. Thus, introducing new and more effective treatment methods, such as biological techniques, is crucial to control the emission of greenhouse gases. Many studies have demonstrated CO2 fixation using photo-bioreactors and raceway ponds, but a comprehensive review is yet to be published on biological CO2 fixation. A comprehensive review of CO2 fixation through biological process is presented in this paper as biological processes are ideal to control both organic and inorganic pollutants. This process can also cover the classification of methods, functional mechanisms, designs, and their operational parameters, which are crucial for efficient CO2 fixation. This review also suggests the bio-trickling filter process as an appropriate approach in CO2 fixation to assist in creating a pollution-free environment. Finally, this paper introduces optimum designs, growth rate models, and CO2 fixation of microalgae, functions, and operations in biological CO2 fixation. PMID:27576148

  3. An overview of biological processes and their potential for CO2 capture.

    PubMed

    Goli, Amin; Shamiri, Ahmad; Talaiekhozani, Amirreza; Eshtiaghi, Nicky; Aghamohammadi, Nasrin; Aroua, Mohamed Kheireddine

    2016-12-01

    The extensive amount of available information on global warming suggests that this issue has become prevalent worldwide. Majority of countries have issued laws and policies in response to this concern by requiring their industrial sectors to reduce greenhouse gas emissions, such as CO2. Thus, introducing new and more effective treatment methods, such as biological techniques, is crucial to control the emission of greenhouse gases. Many studies have demonstrated CO2 fixation using photo-bioreactors and raceway ponds, but a comprehensive review is yet to be published on biological CO2 fixation. A comprehensive review of CO2 fixation through biological process is presented in this paper as biological processes are ideal to control both organic and inorganic pollutants. This process can also cover the classification of methods, functional mechanisms, designs, and their operational parameters, which are crucial for efficient CO2 fixation. This review also suggests the bio-trickling filter process as an appropriate approach in CO2 fixation to assist in creating a pollution-free environment. Finally, this paper introduces optimum designs, growth rate models, and CO2 fixation of microalgae, functions, and operations in biological CO2 fixation.

  4. Radioactive characterization of the main materials involved in the titanium dioxide production process and their environmental radiological impact.

    PubMed

    Mantero, J; Gazquez, M J; Bolivar, J P; Garcia-Tenorio, R; Vaca, F

    2013-06-01

    A study about the distribution of several radionuclides from the uranium and the thorium series radionuclides along the production process of a typical NORM industry devoted to the production of titanium dioxide has been performed. With this end the activity concentrations in raw materials, final product, co-products, and wastes of the production process have been determined by both gamma-ray and alpha-particle spectrometry. The main raw material used in the studied process (ilmenite) presents activity concentrations of around 300 Bq kg(-1) for Th-series radionuclides and 100 Bq kg(-1) for the U-series ones. These radionuclides in the industrial process are distributed in the different steps of the production process according mostly to the chemical behaviour of each radioelement, following different routes. As an example, most of the radium remains associated with the un-dissolved material waste, with activity concentrations around 3 kBq kg(-1) of (228)Ra and around 1 kBq kg(-1) of (226)Ra, while the final commercial products (TiO2 pigments and co-products) contain negligible amounts of radioactivity. The obtained results have allowed assessing the possible public radiological impact associated with the use of the products and co-products obtained in this type of industry, as well as the environmental radiological impact associated with the solid residues and liquid generated discharges.

  5. Capturing Knowledge In Order To Optimize The Cutting Process For Polyethylene Pipes Using Knowledge Models

    NASA Astrophysics Data System (ADS)

    Rotaru, Ionela Magdalena

    2015-09-01

    Knowledge management is a powerful instrument. Areas where knowledge - based modelling can be applied are different from business, industry, government to education area. Companies engage in efforts to restructure the database held based on knowledge management principles as they recognize in it a guarantee of models characterized by the fact that they consist only from relevant and sustainable knowledge that can bring value to the companies. The proposed paper presents a theoretical model of what it means optimizing polyethylene pipes, thus bringing to attention two important engineering fields, the one of the metal cutting process and gas industry, who meet in order to optimize the butt fusion welding process - the polyethylene cutting part - of the polyethylene pipes. All approach is shaped on the principles of knowledge management. The study was made in collaboration with companies operating in the field.

  6. Synapse-specific stabilization of plasticity processes: the synaptic tagging and capture hypothesis revisited 10 years later.

    PubMed

    Barco, Angel; Lopez de Armentia, Mikel; Alarcon, Juan M

    2008-01-01

    A decade ago, the synaptic tagging hypothesis was proposed to explain how newly synthesized plasticity products can be specifically targeted to active synapses. A growing number of studies have validated the seminal findings that gave rise to this model, as well as contributed to unveil and expand the range of mechanisms underlying late-associativity and neuronal computation. Here, we will review what it was learnt during this past decade regarding the cellular and molecular mechanisms underlying synaptic tagging and synaptic capture. The accumulated experimental evidence has widened the theoretical framework set by the synaptic tagging and capture (STC) model and introduced concepts that were originally considered part of alternative models for explaining synapse-specific long-term potentiation (LTP). As a result, we believe that the STC model, now improved and expanded with these new ideas and concepts, still represents the most compelling hypothesis to explain late-associativity in synapse-specific plasticity processes. We will also discuss the impact of this model in our view of the integrative capability of neurons and associative learning. PMID:18281094

  7. Organoclay dispersion in linear low-density polyethylene and maleated linear low-density polyethylene via supercritical carbon dioxide processing

    NASA Astrophysics Data System (ADS)

    Factor, Matthew John

    Research into polymer-clay nanocomposites (PCN’s) has been ongoing for decades as a result of the property enhancements offered by clay. To fully exploit these property enhancements, organically modified clays (organoclays) are utilized to promote clay delamination by reducing the disparity between the hydrophilicity of the clay and the hydrophobicity of the highly used polyolefin polymer. Since the organic modification of organoclays can degrade at temperatures typical to many polymers during melt-mix processing, this work utilizes the low-temperature processing fluid supercritical carbon dioxide (scCO2 ) to disperse an organoclay into the highly used polymer LLDPE and ascertains the associated processing conditions for achieving this goal. Investigations into the LLDPE resin size, scCO2 processing time, scCO2 capability and the processing component compatibility were undertaken to better understand the important parameters to achieving organoclay dispersion, in terms of infusion and intercalation/exfoliation behavior. A LLDPE pellet resin showed improved dispersion and obtainable information over that of a granule resin, securing the choice of resin for subsequent experiments. Experiments undertaken with pellet resin exhibited that a 1-hr processing time was insufficient for organoclay infusion into LLDPE, however when infusion occurs, intercalation/exfoliation can be affected by scCO 2. Increasing the compatibility of LLDPE with clay and the processing fluid revealed that the increased compatibility had altered the effect of scCO2. Further analysis with the 93A-infused samples was conducted in order to gain a better understanding of the effect of scCO2 processing, such as the quantity and size of clay particles dispersed and changes to the polymer incurred by processing.

  8. Biocatalytic carbon capture via reversible reaction cycle catalyzed by isocitrate dehydrogenase.

    PubMed

    Xia, Shunxiang; Frigo-Vaz, Benjamin; Zhao, Xueyan; Kim, Jungbae; Wang, Ping

    2014-09-12

    The practice of carbon capture and storage (CCS) requires efficient capture and separation of carbon dioxide from its gaseous mixtures such as flue gas, followed by releasing it as a pure gas which can be subsequently compressed and injected into underground storage sites. This has been mostly achieved via reversible thermochemical reactions which are generally energy-intensive. The current work examines a biocatalytic approach for carbon capture using an NADP(H)-dependent isocitrate dehydrogenase (ICDH) which catalyzes reversibly carboxylation and decarboxylation reactions. Different from chemical carbon capture processes that rely on thermal energy to realize purification of carbon dioxide, the biocatalytic strategy utilizes pH to leverage the reaction equilibrium, thereby realizing energy-efficient carbon capture under ambient conditions. Results showed that over 25 mol of carbon dioxide could be captured and purified from its gas mixture for each gram of ICDH applied for each carboxylation/decarboxylation reaction cycle by varying pH between 6 and 9. This work demonstrates the promising potentials of pH-sensitive biocatalysis as a green-chemistry route for carbon capture.

  9. Measurements of proton radiative capture cross sections relevant to the astrophysical rp- and γ-processes

    NASA Astrophysics Data System (ADS)

    Chloupek, F. R.; Murphy, A. St J.; Boyd, R. N.; Cole, A. L.; Görres, J.; Guray, R. T.; Raimann, G.; Zach, J. J.; Rauscher, T.; Schwarzenberg, J. V.; Tischhauser, P.; Wiescher, M. C.

    1999-06-01

    Measurements have been made of the 96Zr(p,γ)97Nb, 112Sn(p,γ)113Sb, and 119Sn(p,γ)120Sb cross section excitation functions. Incident proton energies ranged from 2.8 MeV to 8.5 MeV. These reactions are relevant to several processes of stellar nucleosynthesis. The resulting astrophysical S-factors are compared to those from theoretical statistical model calculations using the SMOKER, and the more recent NON-SMOKER, codes to judge their applicability to these reactions.

  10. Comparison of Satellite Observations of Nitrogen Dioxide to Surface Monitor Nitrogen Dioxide Concentration

    NASA Technical Reports Server (NTRS)

    Kleb, Mary M.; Pippin, Margaret R.; Pierce, R. Bradley; Neil, Doreen O.; Lingenfelser, Gretchen; Szykman, James J.

    2006-01-01

    Nitrogen dioxide is one of the U. S. EPA s criteria pollutants, and one of the main ingredients needed for the production of ground-level ozone. Both ozone and nitrogen dioxide cause severe public health problems. Existing satellites have begun to produce observational data sets for nitrogen dioxide. Under NASAs Earth Science Applications Program, we examined the relationship between satellite observations and surface monitor observations of this air pollutant to examine if the satellite data can be used to facilitate a more capable and integrated observing network. This report provides a comparison of satellite tropospheric column nitrogen dioxide to surface monitor nitrogen dioxide concentration for the period from September 1996 through August 1997 at more than 300 individual locations in the continental US. We found that the spatial resolution and observation time of the satellite did not capture the variability of this pollutant as measured at ground level. The tools and processes developed to conduct this study will be applied to the analysis of advanced satellite observations. One advanced instrument has significantly better spatial resolution than the measurements studied here and operates with an afternoon overpass time, providing a more representative distribution for once-per-day sampling of this photochemically active atmospheric constituent.

  11. Efficient utilization of greenhouse gas in a gas-to-liquids process combined with carbon dioxide reforming of methane.

    PubMed

    Ha, Kyoung-Su; Bae, Jong Wook; Woo, Kwang-Jae; Jun, Ki-Won

    2010-02-15

    A process model for a gas-to-liquids (GTL) process mainly producing Fischer-Tropsch (FT) synthetic oils has been developed to assess the effects of reforming methods, recycle ratio of unreacted syngas mixture on the process efficiency and the greenhouse gas (GHG) emission. The reforming unit of our study is composed of both steam reforming of methane (SRM) and carbon dioxide reforming of methane (CDR) to form syngas, which gives composition flexibility, reduction in GHG emission, and higher cost-competitiveness. With recycling, it is found that zero emission of CO(2) from the process can be realized and the required amount of natural gas (NG) can be significantly reduced. This GTL process model has been built by using Aspen Plus software, and it is mainly composed of a feeding unit, a reforming unit, an FT synthesis unit, several separation units and a recycling unit. The composition flexibility of the syngas mixture due to the two different types of reforming reactions raises an issue that in order to attain the optimized feed composition of FT synthesis the amount of flow rate of each component in the fresh feed mixture should be determined considering the effects of the recycle and its split ratio. In the FT synthesis unit, the 15 representative reactions for the chain growth and water gas shift on the cobalt-based catalyst are considered. After FT synthesis, the unreacted syngas mixture is recycled to the reforming unit or the FT synthesis unit or both to enhance process efficiency. The effect of the split ratio, the recycle flow rate to the FT reactor over the recycle flow rate to the reforming unit, on the efficiency of the process was also investigated. This work shows that greater recycle to the reforming unit is less effective than that to the FT synthesis unit from the standpoint of the net heat efficiency of the process, since the reforming reactions are greatly endothermic and greater recycle to the reformer requires more energy.

  12. An Integrated Hydrogen Production-CO2 Capture Process from Fossil Fuel

    SciTech Connect

    Zhicheng Wang

    2007-03-15

    The new technology concept integrates two significant complementary hydrogen production and CO{sub 2}-sequestration approaches that have been developed at Oak Ridge National Laboratory (ORNL) and Clark Atlanta University. The process can convert biomass into hydrogen and char. Hydrogen can be efficiently used for stationary power and mobile applications, or it can be synthesized into Ammonia which can be used for CO{sub 2}-sequestration, while char can be used for making time-release fertilizers (NH{sub 4}HCO{sub 3}) by absorption of CO{sub 2} and other acid gases from exhaust flows. Fertilizers are then used for the growth of biomass back to fields. This project includes bench scale experiments and pilot scale tests. The Combustion and Emission Lab at Clark Atlanta University has conducted the bench scale experiments. The facility used for pilot scale tests was built in Athens, GA. The overall yield from this process is 7 wt% hydrogen and 32 wt% charcoal/activated carbon of feedstock (peanut shell). The value of co-product activated carbon is about $1.1/GJ and this coproduct reduced the selling price of hydrogen. And the selling price of hydrogen is estimated to be $6.95/GJ. The green house experimental results show that the samples added carbon-fertilizers have effectively growth increase of three different types of plants and improvement ability of keeping fertilizer in soil to avoid the fertilizer leaching with water.

  13. ADVANCED OXYFUEL BOILERS AND PROCESS HEATERS FOR COST EFFECTIVE CO2 CAPTURE AND SEQUESTRATION

    SciTech Connect

    Bart van Hassel; John Sirman

    2005-07-01

    This annual technical progress report summarizes the work accomplished during the third year of the program, January-December 2004, in the following task areas: Task 1--Conceptual Design, Task 2--Laboratory Scale Evaluations, Task 3--OTM Development, Task 4--Economic Evaluation and Commercialization Planning and Task 5--Program Management. The groundwork was laid for both the membrane materials development and the construction of the required facilities for testing the membrane reliability and performance. It has resulted in the construction of a single tube and multi-tube combustion test facility. Design for Six Sigma (DFSS) principles were applied to the membrane material selection process. The required ceramic powders were ordered and will be evaluated in 2005. Design of experiment techniques (fuel gas mixture design) were applied to the membrane performance evaluation process. The first results indicate that the oxygen flux of the membrane is significantly higher when the porous support is exposed to the fuel gas mixture instead of air. Failures of the oxygen transport membrane tube did not occur during the reporting period which is supporting evidence that our emphasis on design for robustness is yielding the desired result. All work on the project was performed in a safe manner as proven by zero recordable injuries or lost work days.

  14. Methane capture from livestock manure.

    PubMed

    Tauseef, S M; Premalatha, M; Abbasi, Tasneem; Abbasi, S A

    2013-03-15

    It has been estimated that livestock manure contributes about 240 million metric tons of carbon dioxide equivalent of methane to the atmosphere and represents one of the biggest anthropogenic sources of methane. Considering that methane is the second biggest contributor to global warming after carbon dioxide, it is imperative that ways and means are developed to capture as much of the anthropogenic methane as possible. There is a major associated advantage of methane capture: its use as a source of energy which is comparable in 'cleanness' to natural gas. The present review dwells upon the traditional ways of methane capture used in India, China, and other developing countries for providing energy to the rural poor. It then reviews the present status of methane capture from livestock manure in developed countries and touches upon the prevalent trends.

  15. Capturing a failure of an ASIC in-situ, using infrared radiometry and image processing software

    NASA Technical Reports Server (NTRS)

    Ruiz, Ronald P.

    2003-01-01

    Failures in electronic devices can sometimes be tricky to locate-especially if they are buried inside radiation-shielded containers designed to work in outer space. Such was the case with a malfunctioning ASIC (Application Specific Integrated Circuit) that was drawing excessive power at a specific temperature during temperature cycle testing. To analyze the failure, infrared radiometry (thermography) was used in combination with image processing software to locate precisely where the power was being dissipated at the moment the failure took place. The IR imaging software was used to make the image of the target and background, appear as unity. As testing proceeded and the failure mode was reached, temperature changes revealed the precise location of the fault. The results gave the design engineers the information they needed to fix the problem. This paper describes the techniques and equipment used to accomplish this failure analysis.

  16. Process for CO.sub.2 capture using zeolites from high pressure and moderate temperature gas streams

    DOEpatents

    Siriwardane, Ranjani V.; Stevens, Robert W.

    2012-03-06

    A method for separating CO.sub.2 from a gas stream comprised of CO.sub.2 and other gaseous constituents using a zeolite sorbent in a swing-adsorption process, producing a high temperature CO.sub.2 stream at a higher CO.sub.2 pressure than the input gas stream. The method utilizes CO.sub.2 desorption in a CO.sub.2 atmosphere and effectively integrates heat transfers for optimizes overall efficiency. H.sub.2O adsorption does not preclude effective operation of the sorbent. The cycle may be incorporated in an IGCC for efficient pre-combustion CO.sub.2 capture. A particular application operates on shifted syngas at a temperature exceeding 200.degree. C. and produces a dry CO.sub.2 stream at low temperature and high CO.sub.2 pressure, greatly reducing any compression energy requirements which may be subsequently required.

  17. Optical fibre multi-parameter sensing with secure cloud based signal capture and processing

    NASA Astrophysics Data System (ADS)

    Newe, Thomas; O'Connell, Eoin; Meere, Damien; Yuan, Hongwei; Leen, Gabriel; O'Keeffe, Sinead; Lewis, Elfed

    2016-05-01

    Recent advancements in cloud computing technologies in the context of optical and optical fibre based systems are reported. The proliferation of real time and multi-channel based sensor systems represents significant growth in data volume. This coupled with a growing need for security presents many challenges and presents a huge opportunity for an evolutionary step in the widespread application of these sensing technologies. A tiered infrastructural system approach is adopted that is designed to facilitate the delivery of Optical Fibre-based "SENsing as a Service- SENaaS". Within this infrastructure, novel optical sensing platforms, deployed within different environments, are interfaced with a Cloud-based backbone infrastructure which facilitates the secure collection, storage and analysis of real-time data. Feedback systems, which harness this data to affect a change within the monitored location/environment/condition, are also discussed. The cloud based system presented here can also be used with chemical and physical sensors that require real-time data analysis, processing and feedback.

  18. Drawing as Instrument, Drawings as Evidence: Capturing Mental Processes with Pencil and Paper.

    PubMed

    Puglionesi, Alicia

    2016-07-01

    Researchers in the mind sciences often look to the production and analysis of drawings to reveal the mental processes of their subjects. This essay presents three episodes that trace the emergence of drawing as an instrumental practice in the study of the mind. Between 1880 and 1930, drawings gained currency as a form of scientific evidence - as stable, reproducible signals from a hidden interior. I begin with the use of drawings as data in the child study movement, move to the telepathic transmission of drawings in psychical research and conclude with the development of drawing as an experimental and diagnostic tool for studying neurological impairment. Despite significant shifts in the theoretical and disciplinary organisation of the mind sciences in the early twentieth century, researchers attempted to stabilise the use of subject-generated drawings as evidence by controlling the contexts in which drawings were produced and reproduced, and crafting subjects whose interiority could be effectively circumscribed. While movements such as psychoanalysis and art therapy would embrace the narrative interpretation of patient art, neuropsychology continued to utilise drawings as material traces of cognitive functions. PMID:27292325

  19. Capturing and Processing Soil GHG Fluxes Using the LI-COR LI-8100A

    NASA Astrophysics Data System (ADS)

    Xu, Liukang; McDermitt, Dayle; Hupp, Jason; Johnson, Mark; Madsen, Rod

    2015-04-01

    The LI-COR LI-8100A Automated Soil CO2 Flux System is designed to measure soil CO2 efflux using automated chambers and a non-steady state measurement protocol. While CO2 is an important gas in many contexts, it is not the only gas of interest for many research applications. With some simple plumbing modifications, many third party analyzers capable of measuring other trace gases, e.g. N2O, CH4, or 13CO2 etc., can be interfaced with the LI-8100A System, and LI-COR's data processing software (SoilFluxPro™) can be used to compute fluxes for these additional gases. In this paper we describe considerations for selecting an appropriate third party analyzer to interface with the system, how to integrate data into the system, and the procedure used to compute fluxes of additional gases in SoilFluxPro™. A case study is presented to demonstrate methane flux measurements using an Ultra-Portable Greenhouse Gas Analyzer (Ultra-Portable GGA, model 915-0011), manufactured by Los Gatos Research and integrated into the LI-8100A System. Laboratory and field test results show that the soil CO2 efflux based on the time series of CO2 data measured either with the LI-8100A System or with the Ultra-Portable GGA are essentially the same. This suggests that soil GHG fluxes measured with both systems are reliable.

  20. Drawing as Instrument, Drawings as Evidence: Capturing Mental Processes with Pencil and Paper

    PubMed Central

    Puglionesi, Alicia

    2016-01-01

    Researchers in the mind sciences often look to the production and analysis of drawings to reveal the mental processes of their subjects. This essay presents three episodes that trace the emergence of drawing as an instrumental practice in the study of the mind. Between 1880 and 1930, drawings gained currency as a form of scientific evidence – as stable, reproducible signals from a hidden interior. I begin with the use of drawings as data in the child study movement, move to the telepathic transmission of drawings in psychical research and conclude with the development of drawing as an experimental and diagnostic tool for studying neurological impairment. Despite significant shifts in the theoretical and disciplinary organisation of the mind sciences in the early twentieth century, researchers attempted to stabilise the use of subject-generated drawings as evidence by controlling the contexts in which drawings were produced and reproduced, and crafting subjects whose interiority could be effectively circumscribed. While movements such as psychoanalysis and art therapy would embrace the narrative interpretation of patient art, neuropsychology continued to utilise drawings as material traces of cognitive functions. PMID:27292325

  1. Poly(1,4-phenyleneazine N,N-dioxide): A recyclable material for a solventless laser-imageable resist process

    SciTech Connect

    Baum, T.H.; Larson, C.E.; Hacker, N.P.

    1994-11-01

    Upon heating under vacuum, poly(1,4-phenyleneazine-N,N-dioxide) depolymerizes to give 1,4-dinitrosobenzene which can be condensed onto a suitable substrate. The nature of the condensate is dependent on the substrate temperature. At temperatures below -110{degrees}C the condensate can be monomeric, at about -50{degrees}C it is a mixture of dimer and oligomers, and at -20{degrees}C it is polymeric. Thick and thin films of the polymer can be rapidly prepared by volatilization of 1,4-dinitrosobenzene from the bulk polymer onto a substrate and allowing the collected condensate to warm to room temperature. The resultant films appear to be stable indefinitely at room temperature and atmospheric pressure yet can be selectively removed from the substrate using a focused visible laser beam. After a suitable image-transfer process, the polymer is removed by heating to 100{degrees}C. The laser imaging, deposition, and final removal of polymer are all nondestructive, thermal processes. Thus if a suitable vacuum chamber equipped with a cooling trap is used for this process, the polymer is 100% recyclable. 14 refs., 6 figs.

  2. Carbon dioxide sequestration by direct mineral carbonation: process mineralogy of feed and products

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Rush, G.E.; Dahlin, Cheryl L.; Collins, W. Keith

    2002-05-01

    Direct mineral carbonation was investigated as a process to convert gaseous CO[2] into a geologically stable final form. The process utilizes a slurry of water, with bicarbonate and salt additions, mixed with a mineral reactant, such as olivine (Mg[2]SiO[4]) or serpentine [Mg[3]Si[2]O[5](OH)[4

  3. Full Scale Field Trial of the Low Temperature Mercury Capture Process

    SciTech Connect

    Locke, James; Winschel, Richard

    2012-05-21

    CONSOL Energy Inc., with partial funding from the Department of Energy (DOE) National Energy Technology Laboratory, designed a full-scale installation for a field trial of the Low-Temperature Mercury Control (LTMC) process, which has the ability to reduce mercury emissions from coal-fired power plants by over 90 percent, by cooling flue gas temperatures to approximately 230°F and absorbing the mercury on the native carbon in the fly ash, as was recently demonstrated by CONSOL R&D on a slip-stream pilot plant at the Allegheny Energy Mitchell Station with partial support by DOE. LTMC has the potential to remove over 90 percent of the flue gas mercury at a cost at least an order of magnitude lower (on a $/lb mercury removed basis) than activated carbon injection. The technology is suitable for retrofitting to existing and new plants, and, although it is best suited to bituminous coal-fired plants, it may have some applicability to the full range of coal types. Installation plans were altered and moved from the original project host site, PPL Martins Creek plant, to a second host site at Allegheny Energy's R. Paul Smith plant, before installation actually occurred at the Jamestown (New York) Board of Public Utilities (BPU) Samuel A. Carlson (Carlson) Municipal Generating Station Unit 12, where the LTMC system was operated on a limited basis. At Carlson, over 60% mercury removal was demonstrated by cooling the flue gas to 220-230°F at the ESP inlet via humidification. The host unit ESP operation was unaffected by the humidification and performed satisfactorily at low temperature conditions.

  4. Capturing peripersonal spatial neglect: an electronic method to quantify visuospatial processes.

    PubMed

    Vaes, Nathalie; Lafosse, Christophe; Nys, Gudrun; Schevernels, Hanne; Dereymaeker, Lutgart; Oostra, Kristine; Hemelsoet, Dimitri; Vingerhoets, Guy

    2015-03-01

    Computerized as well as paper-and-pencil tasks are applied in mapping visuospatial neglect in experimental research and clinical practice. This article presents a new kind of computer-based assessment method, using an electronic pen display and user-friendly software. The approach is tailored to specific spatial processes and highlights the usefulness of a pen display in neglect patients. The advantages of the introduced method are illustrated by a recently designed battery of classic, as well as new, types of tests. The development of the appropriate stimuli and the assorted scoring systems is addressed, as well as the resulting types of task implementation and data generation. The diagnostic value of the different visuospatial neglect tests is demonstrated by comparative analyses between a neglect group and a control group. Among the benefits of the proposed assessment method are (1) the opportunity to perform standardized repeated measurements to quantify recovery, (2) online performance monitoring, (3) flexible employment, (4) the collection of exact data over a short period, and (5) the easy availability of more refined quantitative as well as interesting qualitative information, especially as compared to classic or paper-and-pencil tasks. To indicate that this method also lends itself well to measures for treatment procedures, an illustration is given with respect to specific measurements during prism adaptation. The tasks of the Visuospatial Neglect Test Battery and the prism adaptation measures are illustrated by a case study. The outlined applications are discussed with respect to experimental as well as clinical purposes.

  5. Carbon Dioxide Capture Technology Act of 2009

    THOMAS, 111th Congress

    Sen. Barrasso, John [R-WY

    2009-11-05

    12/08/2009 Committee on Energy and Natural Resources Subcommittee on Energy. Hearings held. With printed Hearing: S.Hrg. 111-330. (All Actions) Tracker: This bill has the status IntroducedHere are the steps for Status of Legislation:

  6. CHARGED-PARTICLE AND NEUTRON-CAPTURE PROCESSES IN THE HIGH-ENTROPY WIND OF CORE-COLLAPSE SUPERNOVAE

    SciTech Connect

    Farouqi, K.; Truran, J. W.; Kratz, K.-L.; Pfeiffer, B.; Rauscher, T.; Thielemann, F.-K. E-mail: truran@nova.uchicago.ed E-mail: k-l.Kratz@mpic.d E-mail: F-K.Thielemann@unibas.c

    2010-04-01

    The astrophysical site of the r-process is still uncertain, and a full exploration of the systematics of this process in terms of its dependence on nuclear properties from stability to the neutron drip-line within realistic stellar environments has still to be undertaken. Sufficiently high neutron-to-seed ratios can only be obtained either in very neutron-rich low-entropy environments or moderately neutron-rich high-entropy environments, related to neutron star mergers (or jets of neutron star matter) and the high-entropy wind of core-collapse supernova explosions. As chemical evolution models seem to disfavor neutron star mergers, we focus here on high-entropy environments characterized by entropy S, electron abundance Y{sub e} , and expansion velocity V{sub exp}. We investigate the termination point of charged-particle reactions, and we define a maximum entropy S{sub final} for a given V{sub exp} and Y{sub e} , beyond which the seed production of heavy elements fails due to the very small matter density. We then investigate whether an r-process subsequent to the charged-particle freeze-out can in principle be understood on the basis of the classical approach, which assumes a chemical equilibrium between neutron captures and photodisintegrations, possibly followed by a beta-flow equilibrium. In particular, we illustrate how long such a chemical equilibrium approximation holds, how the freeze-out from such conditions affects the abundance pattern, and which role the late capture of neutrons originating from beta-delayed neutron emission can play. Furthermore, we analyze the impact of nuclear properties from different theoretical mass models on the final abundances after these late freeze-out phases and beta-decays back to stability. As only a superposition of astrophysical conditions can provide a good fit to the solar r-abundances, the question remains how such superpositions are attained, resulting in the apparently robust r-process pattern observed in low

  7. Charged-partricle and neutron-capture processes in the high-entropy wind of core-collapse supernovae.

    SciTech Connect

    Farouqi, K.; Kratz, K.-L.; Pfeiffer, B.; Rauscher, T.; Thielemann, F.-K.; Truran, J. W.; Physics; Univ. of Chicago; Joint Inst. for Nuclear Astrophysics; Univ. Mainz; Virtual Inst. for Nuclear Structure and Astrophysics; Max-Planck-Inst. fur Chemie; Univ. of Basel

    2010-04-01

    The astrophysical site of the r-process is still uncertain, and a full exploration of the systematics of this process in terms of its dependence on nuclear properties from stability to the neutron drip-line within realistic stellar environments has still to be undertaken. Sufficiently high neutron-to-seed ratios can only be obtained either in very neutron-rich low-entropy environments or moderately neutron-rich high-entropy environments, related to neutron star mergers (or jets of neutron star matter) and the high-entropy wind of core-collapse supernova explosions. As chemical evolution models seem to disfavor neutron star mergers, we focus here on high-entropy environments characterized by entropy S, electron abundance Y{sub e}, and expansion velocity V{sub exp}. We investigate the termination point of charged-particle reactions, and we define a maximum entropy S{sub final} for a given V{sub exp} and Y{sub e}, beyond which the seed production of heavy elements fails due to the very small matter density. We then investigate whether an r-process subsequent to the charged-particle freeze-out can in principle be understood on the basis of the classical approach, which assumes a chemical equilibrium between neutron captures and photodisintegrations, possibly followed by a {beta}-flow equilibrium. In particular, we illustrate how long such a chemical equilibrium approximation holds, how the freeze-out from such conditions affects the abundance pattern, and which role the late capture of neutrons originating from {beta}-delayed neutron emission can play. Furthermore, we analyze the impact of nuclear properties from different theoretical mass models on the final abundances after these late freeze-out phases and {beta}-decays back to stability. As only a superposition of astrophysical conditions can provide a good fit to the solar r-abundances, the question remains how such superpositions are attained, resulting in the apparently robust r-process pattern observed in low

  8. Charged-particle and neutron-capture processes in the high-entropy wind of core-collapse supernovae.

    SciTech Connect

    Farouqi, K.; Kratz, K.-L.; Pfeiffer, B.; Rauscher, T.; Thielemann, F.-K.; Truran, J.W.; Physics; Univ. of Chicago; Joint Inst. for Nuclear Astrophysics; Univ. Mainz; Virtual Inst. for Nuclear Structure and Astrophysics; Max-Planck-Insti. fur Chemie; Univ. of Basel

    2010-04-01

    The astrophysical site of the r-process is still uncertain, and a full exploration of the systematics of this process in terms of its dependence on nuclear properties from stability to the neutron drip-line within realistic stellar environments has still to be undertaken. Sufficiently high neutron-to-seed ratios can only be obtained either in very neutron-rich low-entropy environments or moderately neutron-rich high-entropy environments, related to neutron star mergers (or jets of neutron star matter) and the high-entropy wind of core-collapse supernova explosions. As chemical evolution models seem to disfavor neutron star mergers, we focus here on high-entropy environments characterized by entropy S, electron abundance Y{sub e}, and expansion velocity V{sub exp}. We investigate the termination point of charged-particle reactions, and we define a maximum entropy S{sub final} for a given V{sub exp} and Y{sub e}, beyond which the seed production of heavy elements fails due to the very small matter density. We then investigate whether an r-process subsequent to the charged-particle freeze-out can in principle be understood on the basis of the classical approach, which assumes a chemical equilibrium between neutron captures and photodisintegrations, possibly followed by a {beta}-flow equilibrium. In particular, we illustrate how long such a chemical equilibrium approximation holds, how the freeze-out from such conditions affects the abundance pattern, and which role the late capture of neutrons originating from {beta}-delayed neutron emission can play. Furthermore, we analyze the impact of nuclear properties from different theoretical mass models on the final abundances after these late freeze-out phases and {beta}-decays back to stability. As only a superposition of astrophysical conditions can provide a good fit to the solar r-abundances, the question remains how such superpositions are attained, resulting in the apparently robust r-process pattern observed in low

  9. Cryogenic Carbon Capture

    SciTech Connect

    2010-07-15

    IMPACCT Project: SES is developing a process to capture CO2 from the exhaust gas of coal-fired power plants by desublimation - the conversion of a gas to a solid. Capturing CO2 as a solid and delivering it as a liquid avoids the large energy cost of CO2 gas compression. SES’ capture technology facilitates the prudent use of available energy resources. Coal is our most abundant energy resource and is an excellent fuel for baseline power production. SES capture technology can capture 99% of the CO2 emissions in addition to a wide range of other pollutants more efficiently and at lower costs than existing capture technologies. SES’ capture technology can be readily added to our existing energy infrastructure.

  10. Process Design for the Biocatalysis of Value-Added Chemicals from Carbon Dioxide

    SciTech Connect

    Mark A. Eiteman

    2006-07-31

    This report describes results toward developing a process to sequester CO{sub 2} centered on the enzyme pyruvate carboxylase. The process involves the use of bacteria to convert CO{sub 2} and glucose as a co-substrate and generates succinic acid as a commodity chemical product. The phases of research have included strain development and process development. Though we continue to work on one important component of strain development, the research has principally focused on process development. In the previous year we constructed several strains which would serve as templates for the CO{sub 2} sequestration, including the knock-out of genes involved in the formation of undesirable byproducts. This project period the focus has been on the integration of the pyruvate carboxylase gene (pyc) onto the E. coli chromosome. This has proven to be a difficult task because of relatively low expression of the gene and resulting low enzyme activity when only one copy of the gene is present on the chromosome. Several molecular biology techniques have been applied, with some success, to improve the level of protein activity as described herein. Progress in process development has come as a result of conducting numerous fermentation experiments to select optimal conditions for CO{sub 2} sequestration. This process-related research has progressed in four areas. First, we have clarified the range of pH which results in the optimal rate of sequestration. Second, we have determined how the counterion used to control the pH affects the sequestration rate. Third, we have determined how CO{sub 2} gas phase composition impacts sequestration rate. Finally, we have made progress in determining the affect of several potential gaseous impurities on CO{sub 2} sequestration; in particular we have completed a study using NO{sub 2}. Although the results provide significant guidance as to process conditions for CO{sub 2} sequestration and succinate production, in some cases we do not yet understand

  11. Process Design for the Biocatalysis of Value-Added Chemicals from Carbon Dioxide

    SciTech Connect

    Mark Eiteman

    2007-07-31

    This report describes results toward developing a process to sequester CO{sub 2} centered on the enzymes PEP carboxylase and pyruvate carboxylase. The process involves the use of bacteria to convert CO{sub 2} and glucose as a co-substrate and generates succinic acid as a commodity chemical product. The study reports on strain development and process development. In the area of strain development, knockouts in genes which divert carbon from the enzymatic steps involved in CO{sub 2} consumption were completed, and were shown not to affect significantly the rate of CO{sub 2} sequestration and succinic acid generation. Furthermore, the pyc gene encoding for pyruvate carboxylase proved to be unstable when integrated onto the chromosome. In the area of process development, an optimal medium, pH and base counterion were obtained, leading to a sequestration rate as great as 800 mg/Lh. Detailed studies of gas phase composition demonstrated that CO{sub 2} composition has a significant affect on CO{sub 2} sequestration, while the presence of 'toxic' compounds in the gas, including NO{sub 2}, CO and SO{sub 2} did not have a detrimental effect on sequestration. Some results on prolonging the rate of sequestration indicate that enzyme activities decrease with time, suggesting methods to prolong enzyme activity may benefit the overall process.

  12. Process Design for the Biocatalysis of Value-Added Chemicals from Carbon Dioxide

    SciTech Connect

    Mark A. Eiteman

    2005-11-01

    This report describes results toward developing a process to sequester CO{sub 2} centered on the enzyme pyruvate carboxylase. The process involves the use of bacteria to convert CO{sub 2} and glucose as a co-substrate and generates succinic acid as a commodity chemical product. The first phase of this research has focused on strain development and on process development. Progress in strain development has been made in three areas. The gene encoding for alcohol dehydrogenase has been ''knocked out'' of the bacteria, and thereby eliminating the synthesis of the by-product ethanol. The gene for glucokinase has been overexpressed in the production strain with the goal of faster utilization of glucose (and hence CO{sub 2}). Efforts have continued toward integrating pyruvate carboxylase gene (pyc) onto the E. coli chromosome. Progress in process development has come in conducting several dozen fermentation experiments to find a defined medium that would be successful for the growth of the bacteria, while permitting a high rate of CO{sub 2} utilization in a subsequent prolonged production phase. Using this defined medium, the strains that continue to be constructed are being compared for CO{sub 2} utilization, so that we may understand the factors that govern the biological sequestration process.

  13. An application of CAMx process analysis tools: Exploring process contributions to extreme ozone, nitrogen oxides and sulfur dioxide

    NASA Astrophysics Data System (ADS)

    Murray, David-anthony

    The University at Albany Air Quality Forecasting Modeling System (AQFMS) is a state-of-the-art model that generates reliable daily and "day-ahead" air quality forecasts for the Northeastern United States. The three major categories of processes which dictate regional air quality are production from emission sources, horizontal and vertical transport driven by the prevailing meteorology, and chemical transformations. The Advanced Research WRF (ARW) produces meteorological fields. The Sparse Matrix Operator for Kernel Emissions (SMOKE) processes available emission inventories for air quality modeling. The Comprehensive Air Quality Model with extension (CAMx) handles both chemical processes and the integration of ARW-WRF and SMOKE in devising separate quantitative contributions to pollutant concentrations from process categories. An AQFMS forecast, though indicative of the temporal and spatial changes in the ambient condition, does not tell us exactly how and why those changes occurred. High concentrations of criteria pollutants during "extreme" conditions could come about in many ways. Process analysis takes a step back in numerical procedures to showcase the partial contribution of 18 different processes to the predicted concentration. Area and point source make up the two emission source processes. Advection and diffusion through the west, east, south, north, bottom and top boundary make up the twelve horizontal and vertical transport processes. Gas phase and heterogeneous chemistry make up the two chemical transformation processes, with dry and wet deposition making up the two physio-chemical removal processes. A group of model defined "extreme" intra-day periods in a 12km by 12km grid spacing over The New York Botanical Gardens were evaluated for model performance at the surface and characterized by distinctive modes in which the aforementioned processes contribute to SO2, NOx and O3 concentrations in the vertical layers up to the first 4km of the model

  14. Membrane-based systems for carbon capture and hydrogen purification

    SciTech Connect

    Berchtold, Kathryn A

    2010-11-24

    This presentation describes the activities being conducted at Los Alamos National Laboratory to develop carbon capture technologies for power systems. This work is aimed at continued development and demonstration of a membrane based pre- and post-combustion carbon capture technology and separation schemes. Our primary work entails the development and demonstration of an innovative membrane technology for pre-combustion capture of carbon dioxide that operates over a broad range of conditions relevant to the power industry while meeting the US DOE's Carbon Sequestration Program goals of 90% CO{sub 2} capture at less than a 10% increase in the cost of energy services. Separating and capturing carbon dioxide from mixed gas streams is a first and critical step in carbon sequestration. To be technically and economically viable, a successful separation method must be applicable to industrially relevant gas streams at realistic temperatures and pressures as well as be compatible with large gas volumes. Our project team is developing polymer membranes based on polybenzimidazole (PBI) chemistries that can purify hydrogen and capture CO{sub 2} at industrially relevant temperatures. Our primary objectives are to develop and demonstrate polymer-based membrane chemistries, structures, deployment platforms, and sealing technologies that achieve the critical combination of high selectivity, high permeability, chemical stability, and mechanical stability all at elevated temperatures (> 150 C) and packaged in a scalable, economically viable, high area density system amenable to incorporation into an advanced Integrated Gasification Combined-Cycle (IGCC) plant for pre-combustion CO{sub 2} capture. Stability requirements are focused on tolerance to the primary synthesis gas components and impurities at various locations in the IGCC process. Since the process stream compositions and conditions (temperature and pressure) vary throughout the IGCC process, the project is focused on the

  15. A calcium oxide sorbent process for bulk separation of carbon dioxide

    SciTech Connect

    Silaban, A.; Narcida, M.; Harrison, D.P.

    1992-02-01

    The expected commercialization of coal gasification technology in the US and world-wide will create a need for advanced gas purification and separation processes capable of operating at higher temperatures and in more hostile environments than is common today. For example, a high-temperature, high-pressure process capable of separating CO{sub 2} from coal-derived gas may find application in purifying synthesis gas for H{sub 2}, NH{sub 3}, or CH{sub 3}OH production. High temperature CO{sub 2} removal has the potential for significantly improving the operating efficiency of integrated gasification-molten carbonate fuel cells for electric power generation. This study proved the technical feasibility of a CO{sub 2}-separation process based upon the regenerable noncatalytic gas-solid reaction between CaO and CO{sub 2} to form CACO{sub 3}. Such a process operating at 650{degree}C and 15 atm with 15% CO{sub 2} in the coal gas has the potential for removing in excess of 99% of the CO{sub 2} fed. Selection of a sorbent precursor which, upon calcination, produces high-porosity CaO is important for achieving rapid and complete reaction. The addition of magnesium to the sorbent appears to improve the multicycle durability at a cost of reduced CO{sub 2} capacity per unit mass of sorbent. Reaction conditions, principally calcination and carbonation temperatures, are important factors in multicycle durability. Reaction pressure and CO{sub 2} concentration are important in so far as the initial rapid reaction rate is concerned, but are relatively unimportant in terms of sorbent capacity and durability. Indirect evidence for the simultaneous occurrence of the shift reaction and CO{sub 2}-removal reaction creates the possibility of a direct one-step process for the production of hydrogen from coal-derived gas.

  16. Process for capturing CO2 arising from the calcination of the CaCO3 used in cement manufacture.

    PubMed

    Rodríguez, N; Alonso, M; Grasa, G; Abanades, J Carlos

    2008-09-15

    This paper outlines a new CaCO3 calcination method for producing a stream of CO2 (suitable for permanent geological storage after purification and compression). The process is based on the use of very hot CaO particles (T >1000 degrees C) to transfer heat from a circulating fluidized bed combustor (CFBC) to a calciner (fluidized with CO2 and/or steam). Since the fluidized bed combustor and calciner have separate atmospheres, the CO2 resulting from the decomposition of CaCO3 can be captured, while the CO2 generated in the combustion of the fuel in air is emitted to the atmosphere. We demonstrate that with this system it is possible to reduce the CO2 emissions of a cement plant by around 60%. Furthermore, since the key pieces of equipment are similar to the commercial CFBCs used in power generation plants, it is possible to establish the additional investment required for the system and to estimate the cost per ton of CO2 avoided for this process to be about 19 $/tCO2 avoided.

  17. Process for capturing CO2 arising from the calcination of the CaCO3 used in cement manufacture.

    PubMed

    Rodríguez, N; Alonso, M; Grasa, G; Abanades, J Carlos

    2008-09-15

    This paper outlines a new CaCO3 calcination method for producing a stream of CO2 (suitable for permanent geological storage after purification and compression). The process is based on the use of very hot CaO particles (T >1000 degrees C) to transfer heat from a circulating fluidized bed combustor (CFBC) to a calciner (fluidized with CO2 and/or steam). Since the fluidized bed combustor and calciner have separate atmospheres, the CO2 resulting from the decomposition of CaCO3 can be captured, while the CO2 generated in the combustion of the fuel in air is emitted to the atmosphere. We demonstrate that with this system it is possible to reduce the CO2 emissions of a cement plant by around 60%. Furthermore, since the key pieces of equipment are similar to the commercial CFBCs used in power generation plants, it is possible to establish the additional investment required for the system and to estimate the cost per ton of CO2 avoided for this process to be about 19 $/tCO2 avoided. PMID:18853819

  18. Activation of mass transfer processes at spark plasma sintering of zirconium dioxide

    NASA Astrophysics Data System (ADS)

    Akarachkin, S. A.; Ivashutenko, A. S.; Martyushev, N. V.

    2016-04-01

    The paper presents the results of numerical simulation of thermal and electric fields' distribution in the graphite moulding tool and in the sintered sample of ZrO2-4%Y2O3 in the course of spark plasma sintering (SPS). The reduction of SPS duration is accounted for the largeness of specific thermal flux towards the sample surface, emitted by the graphite moulding tool. The impact of the electric field on the sample structure leads to emergence of the polarizing processes forcing zirconium ions to shift from lattice sites, which is able to reduce the required value of thermal energy necessary for initiation of a diffusion process. The axial pressure at high temperatures of sintering can lead to plastic deformation of the powder particles.

  19. Inhalation of 7.5% carbon dioxide increases threat processing in humans.

    PubMed

    Garner, Matthew; Attwood, Angela; Baldwin, David S; James, Alexandra; Munafò, Marcus R

    2011-07-01

    Inhalation of 7.5% CO(2) increases anxiety and autonomic arousal in humans, and elicits fear behavior in animals. However, it is not known whether CO(2) challenge in humans induces dysfunction in neurocognitive processes that characterize generalized anxiety, notably selective attention to environmental threat. Healthy volunteers completed an emotional antisaccade task in which they looked toward or away from (inhibited) negative and neutral stimuli during inhalation of 7.5% CO(2) and air. CO(2) inhalation increased anxiety, autonomic arousal, and erroneous eye movements toward threat on antisaccade trials. Autonomic response to CO(2) correlated with hypervigilance to threat (speed to initiate prosaccades) and reduced threat inhibition (increased orienting toward and slower orienting away from threat on antisaccade trials) independent of change in mood. Findings extend evidence that CO(2) triggers fear behavior in animals via direct innervation of a distributed fear network that mobilizes the detection of and allocation of processing resources toward environmental threat in humans.

  20. A calcium oxide sorbent process for bulk separation of carbon dioxide

    SciTech Connect

    Harrison, D.P.

    1992-10-01

    Objective is to investigate the feasibility of a high-temperature, high-pressure process for bulk separation of CO[sub 2] from coal- derived gas. An electrobalance reactor was used in Phase I; in Phase II, the switch was made to a fixed-bed reactor with capability for feed and product gas analysis. A gas chromatograph was delivered, installed, and operator training carried out. The sampling valve sequence is discussed.

  1. Processes regulating progressive nitrogen limitation under elevated carbon dioxide: a meta-analysis

    NASA Astrophysics Data System (ADS)

    Liang, J.; Qi, X.; Souza, L.; Luo, Y.

    2015-10-01

    Nitrogen (N) cycle has the potential to regulate climate change through its influence on carbon (C) sequestration. Although extensive researches have been done to explore whether or not progressive N limitation (PNL) occurs under CO2 enrichment, a comprehensive assessment of the processes that regulate PNL is still lacking. Here, we quantitatively synthesized the responses of all major processes and pools in terrestrial N cycle with meta-analysis of CO2 experimental data available in the literature. The results showed that CO2 enrichment significantly increased N sequestration in plant and litter pools but not in soil pool. Thus, the basis of PNL occurrence partially exists. However, CO2 enrichment also significantly increased the N influx via biological N fixation, but decreased the N efflux via leaching. In addition, no general diminished CO2 fertilization effect on plant growth over time was observed. Overall, our analyses suggest that the extra N supply by the increased biological N fixation and decreased leaching may potentially alleviate PNL under elevated CO2 conditions. Moreover, our synthesis showed that CO2 enrichment increased soil ammonium (NH4+) but decreased nitrate (NO3-). The different responses of NH4+ and NO3-, and the consequent biological processes, may result in changes in soil microenvironment, community structures and above-belowground interactions, which could potentially affect the terrestrial biogeochemical cycles and the feedback to climate change.

  2. Laboratory differential simulation design method of pressure absorbers for carbonization of phenolate solution by carbon dioxide in coal-tar processing

    SciTech Connect

    Linek, V.; Sinkule, J.; Moucha, T.; Rejl, J.F.

    2009-01-15

    A laboratory differential simulation method is used for the design of carbonization columns at coal-tar processing in which phenols are regenerated from phenolate solution by carbon dioxide absorption. The design method is based on integration of local absorption rates of carbon dioxide along the column. The local absorption rates into industrial phenolate mixture are measured in a laboratory model contactor for various compositions of the gas and liquid phases under the conditions that ensure the absorption rates in the laboratory absorber simulate the local rates in the industrial column. On the bases of the calculations, two-step carbonization columns were designed for 30000 t/year of the phenolate solution treatment by carbon dioxide. The absorption proceeds at higher pressure of 500 kPa and temperatures from 50 to 65 C, pure carbon dioxide is used and toluene is added. These conditions have the following favourable effects: (I) significant size reduction of the columns, (ii) it is possible to process more concentrated solutions without danger of silting the columns by crystallization of NaHCO{sub 3} on the packing. (iii) small amount of inert gas is released, (iv) lower alkalinity and better separability of the organic phase (phenols with toluene) from water phase (soda or bicarbonate solution) in separators.

  3. Carbon Capture and Storage

    SciTech Connect

    Friedmann, S

    2007-10-03

    Carbon capture and sequestration (CCS) is the long-term isolation of carbon dioxide from the atmosphere through physical, chemical, biological, or engineered processes. This includes a range of approaches including soil carbon sequestration (e.g., through no-till farming), terrestrial biomass sequestration (e.g., through planting forests), direct ocean injection of CO{sub 2} either onto the deep seafloor or into the intermediate depths, injection into deep geological formations, or even direct conversion of CO{sub 2} to carbonate minerals. Some of these approaches are considered geoengineering (see the appropriate chapter herein). All are considered in the 2005 special report by the Intergovernmental Panel on Climate Change (IPCC 2005). Of the range of options available, geological carbon sequestration (GCS) appears to be the most actionable and economic option for major greenhouse gas reduction in the next 10-30 years. The basis for this interest includes several factors: (1) The potential capacities are large based on initial estimates. Formal estimates for global storage potential vary substantially, but are likely to be between 800 and 3300 Gt of C (3000 and 10,000 Gt of CO{sub 2}), with significant capacity located reasonably near large point sources of the CO{sub 2}. (2) GCS can begin operations with demonstrated technology. Carbon dioxide has been separated from large point sources for nearly 100 years, and has been injected underground for over 30 years (below). (3) Testing of GCS at intermediate scale is feasible. In the US, Canada, and many industrial countries, large CO{sub 2} sources like power plants and refineries lie near prospective storage sites. These plants could be retrofit today and injection begun (while bearing in mind scientific uncertainties and unknowns). Indeed, some have, and three projects described here provide a great deal of information on the operational needs and field implementation of CCS. Part of this interest comes from several

  4. Processes regulating progressive nitrogen limitation under elevated carbon dioxide: a meta-analysis

    NASA Astrophysics Data System (ADS)

    Liang, Junyi; Qi, Xuan; Souza, Lara; Luo, Yiqi

    2016-05-01

    The nitrogen (N) cycle has the potential to regulate climate change through its influence on carbon (C) sequestration. Although extensive research has explored whether or not progressive N limitation (PNL) occurs under CO2 enrichment, a comprehensive assessment of the processes that regulate PNL is still lacking. Here, we quantitatively synthesized the responses of all major processes and pools in the terrestrial N cycle with meta-analysis of CO2 experimental data available in the literature. The results showed that CO2 enrichment significantly increased N sequestration in the plant and litter pools but not in the soil pool, partially supporting one of the basic assumptions in the PNL hypothesis that elevated CO2 results in more N sequestered in organic pools. However, CO2 enrichment significantly increased the N influx via biological N fixation and the loss via N2O emission, but decreased the N efflux via leaching. In addition, no general diminished CO2 fertilization effect on plant growth was observed over time up to the longest experiment of 13 years. Overall, our analyses suggest that the extra N supply by the increased biological N fixation and decreased leaching may potentially alleviate PNL under elevated CO2 conditions in spite of the increases in plant N sequestration and N2O emission. Moreover, our syntheses indicate that CO2 enrichment increases soil ammonium (NH4+) to nitrate (NO3-) ratio. The changed NH4+/NO3- ratio and subsequent biological processes may result in changes in soil microenvironments, above-belowground community structures and associated interactions, which could potentially affect the terrestrial biogeochemical cycles. In addition, our data synthesis suggests that more long-term studies, especially in regions other than temperate ones, are needed for comprehensive assessments of the PNL hypothesis.

  5. Processes regulating progressive nitrogen limitation under elevated carbon dioxide: a meta-analysis

    DOE PAGESBeta

    Liang, Junyi; Qi, Xuan; Souza, Lara; Luo, Yiqi

    2016-05-10

    The nitrogen (N) cycle has the potential to regulate climate change through its influence on carbon (C) sequestration. Although extensive research has explored whether or not progressive N limitation (PNL) occurs under CO2 enrichment, a comprehensive assessment of the processes that regulate PNL is still lacking. Here, we quantitatively synthesized the responses of all major processes and pools in the terrestrial N cycle with meta-analysis of CO2 experimental data available in the literature. The results showed that CO2 enrichment significantly increased N sequestration in the plant and litter pools but not in the soil pool, partially supporting one of themore » basic assumptions in the PNL hypothesis that elevated CO2 results in more N sequestered in organic pools. However, CO2 enrichment significantly increased the N influx via biological N fixation and the loss via N2O emission, but decreased the N efflux via leaching. In addition, no general diminished CO2 fertilization effect on plant growth was observed over time up to the longest experiment of 13 years. Overall, our analyses suggest that the extra N supply by the increased biological N fixation and decreased leaching may potentially alleviate PNL under elevated CO2 conditions in spite of the increases in plant N sequestration and N2O emission. Moreover, our syntheses indicate that CO2 enrichment increases soil ammonium (NH4+) to nitrate (NO3−) ratio. The changed NH4+/NO3− ratio and subsequent biological processes may result in changes in soil microenvironments, above-belowground community structures and associated interactions, which could potentially affect the terrestrial biogeochemical cycles. In addition, our data synthesis suggests that more long-term studies, especially in regions other than temperate ones, are needed for comprehensive assessments of the PNL hypothesis.« less

  6. Biodiesel production with continuous supercritical process: non-catalytic transesterification and esterification with or without carbon dioxide.

    PubMed

    Tsai, Yu-Ting; Lin, Ho-mu; Lee, Ming-Jer

    2013-10-01

    The non-catalytic transesterification of refined sunflower oil with supercritical methanol, in the presence of carbon dioxide, was conducted in a tubular reactor at temperatures from 553.2 to 593.2K and pressures up to 25.0 MPa. The FAME yield can be achieved up to about 0.70 at 593.2 K and 10.0 MPa in 23 min with methanol:oil of 25:1 in molar ratio. The effect of adding CO2 on the FAME yield is insignificant. The kinetic behavior of the non-catalytic esterification and transesterification of oleic acid or waste cooking oil (WCO) with supercritical methanol was also investigated. By using the supercritical process, the presence of free fatty acid (FFA) in WCO gives positive contribution to FAME production. The FAME yield of 0.90 from WCO can be achieved in 13 min at 573.2K. The kinetic data of supercritical transesterification and esterifaication were correlated well with a power-law model.

  7. Effect of food processing organic matter on photocatalytic bactericidal activity of titanium dioxide (TiO2).

    PubMed

    Yemmireddy, Veerachandra K; Hung, Yen-Con

    2015-07-01

    The purpose of this study was to determine the effect of food processing organic matter on photocatalytic bactericidal activity of titanium dioxide (TiO2) nanoparticles (NPs). Produce and meat processing wash solutions were prepared using romaine lettuce and ground beef samples. Physico-chemical properties such as pH, turbidity, chemical oxygen demand (COD), total phenolics (for produce) and protein (for meat) content of the extracts were determined using standard procedures. The photocatalytic bactericidal activity of TiO2 (1 mg/mL) in suspension with or without organic matter against Escherichia coli O157:H7 (5-strain) was determined over a period of 3h. Increasing the concentration of organic matter (either produce or meat) from 0% to 100% resulted in 85% decrease in TiO2 microbicidal efficacy. 'Turbidity, total phenolics, and protein contents in wash solutions had significant effect on the log reduction. Increasing the total phenolics content in produce washes from 20 to 114 mg/L decreased the log reduction from 2.7 to 0.38 CFU/mL, whereas increasing the protein content in meat washes from 0.12 to 1.61 mg/L decreased the log reduction from and 5.74 to 0.87 CFU/mL. Also, a linear correlation was observed between COD and total phenolics as well as COD and protein contents. While classical disinfection kinetic models failed to predict, an empirical equation in the form of "Y=me(nX)" (where Y is log reduction, X is COD, and m and n are reaction rate constants) predicted the disinfection kinetics of TiO2 in the presence of organic matter (R(2)=94.4). This study successfully identified an empirical model with COD as a predictor variable to predict the bactericidal efficacy of TiO2 when used in food processing environment.

  8. Reaction Mechanism for m-Xylene Oxidation in the Claus Process by Sulfur Dioxide.

    PubMed

    Sinha, Sourab; Raj, Abhijeet; Al Shoaibi, Ahmed S; Chung, Suk Ho

    2015-09-24

    In the Claus process, the presence of aromatic contaminants such benzene, toluene, and xylenes (BTX), in the H2S feed stream has a detrimental effect on catalytic reactors, where BTX form soot particles and clog and deactivate the catalysts. Among BTX, xylenes are proven to be most damaging contaminant for catalysts. BTX oxidation in the Claus furnace, before they enter catalyst beds, provides a solution to this problem. A reaction kinetics study on m-xylene oxidation by SO2, an oxidant present in Claus furnace, is presented. The density functional theory is used to study the formation of m-xylene radicals (3-methylbenzyl, 2,6-dimethylphenyl, 2,4-dimethylphenyl, and 3,5-dimethylphenyl) through H-abstraction and their oxidation by SO2. The mechanism begins with SO2 addition on the radicals through an O-atom rather than the S-atom with the release of 180.0-183.1 kJ/mol of reaction energies. This exothermic reaction involves energy barriers in the range 3.9-5.2 kJ/mol for several m-xylene radicals. Thereafter, O-S bond scission takes place to release SO, and the O-atom remaining on aromatics leads to CO formation. Among four m-xylene radicals, the resonantly stabilized 3-methylbenzyl exhibited the lowest SO2 addition and SO elimination rates. The reaction rate constants are provided to facilitate Claus process simulations to find conditions suitable for BTX oxidation. PMID:26334187

  9. Reaction Mechanism for m-Xylene Oxidation in the Claus Process by Sulfur Dioxide.

    PubMed

    Sinha, Sourab; Raj, Abhijeet; Al Shoaibi, Ahmed S; Chung, Suk Ho

    2015-09-24

    In the Claus process, the presence of aromatic contaminants such benzene, toluene, and xylenes (BTX), in the H2S feed stream has a detrimental effect on catalytic reactors, where BTX form soot particles and clog and deactivate the catalysts. Among BTX, xylenes are proven to be most damaging contaminant for catalysts. BTX oxidation in the Claus furnace, before they enter catalyst beds, provides a solution to this problem. A reaction kinetics study on m-xylene oxidation by SO2, an oxidant present in Claus furnace, is presented. The density functional theory is used to study the formation of m-xylene radicals (3-methylbenzyl, 2,6-dimethylphenyl, 2,4-dimethylphenyl, and 3,5-dimethylphenyl) through H-abstraction and their oxidation by SO2. The mechanism begins with SO2 addition on the radicals through an O-atom rather than the S-atom with the release of 180.0-183.1 kJ/mol of reaction energies. This exothermic reaction involves energy barriers in the range 3.9-5.2 kJ/mol for several m-xylene radicals. Thereafter, O-S bond scission takes place to release SO, and the O-atom remaining on aromatics leads to CO formation. Among four m-xylene radicals, the resonantly stabilized 3-methylbenzyl exhibited the lowest SO2 addition and SO elimination rates. The reaction rate constants are provided to facilitate Claus process simulations to find conditions suitable for BTX oxidation.

  10. Synthesis of high-surface-area titanium dioxide by sol-gel process for DSSC

    NASA Astrophysics Data System (ADS)

    Wahyuningsih, S.; Ramelan, A. H.; Juliana, G.; Khoirunisa, A. R.; Rahardjo, S. B.; Pramono, E.; Suharyana, S.; Suryana, R.; Supriyanto, A.

    2014-05-01

    Mesoporous TiO2 material was synthesized from dissolution ilmenite as well as from titanium chloride precursor via a sol-gel process in acidic aqueous solution. The properties of these materials were characterized with several analytical techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), wide angle X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, and Barrett-Joyner-Halenda (BJH) analysis. The mesoporous TiO2 materials calcinated at various temperatures were found to have high value surface areas. The photovoltaic of photo-anode build from the mesoporous TiO2 was characterized with I-V Keitley Multimeter, and it was found that photovoltaics fabricated using the mesoporous TiO2 have a good performance. Such a high photovoltaic activity is explained with large surface area and small crystal size.

  11. Molecular level energy and electron transfer processes at nanocrystalline titanium dioxide interfaces

    NASA Astrophysics Data System (ADS)

    Farzad, Fereshteh

    This thesis describes photo-induced molecular electron and energy transfer processes occurring at nanocrystalline semiconductor interfaces. The Introductory Chapter provides background and describes how these materials may be useful for solar energy conversion. In Chapter 2, results describing excitation of Ru(deeb)(bpy)2 2+, bis(2,2'-bipyridine)(2,2'-bipyridine-4,4 '-diethylester)ruthenium(II) hexafluorophosphate, bound to nanocrystalline TiO2 thin films, immersed in an acetonitrile bath are presented. The data indicates that light excitation forms predominately long-lived metal-to-ligand charge-transfer, MLCT, excited states under these conditions. Modeling of the data as a function of irradiance has been accomplished assuming parallel unimolecular and bimolecular excited state deactivation processes. The quantum yield for excited state formation depends on the excitation irradiance, consistent with triplet-triplet annihilation processes that occur with k > 1 x 108 s-1. Chapter 3 extends the work described in Chapter 2 to LiClO4 acetonitrile solutions. Li+ addition results in a red shift in the MLCT absorption and photoluminescence, PL, and a concentration dependent quenching of the PL intensity on TiO2. The Li+ induced spectroscopic changes were found to be reversible by varying the electrolyte composition. A second-order kinetic model quantified charge recombination transients. A model is proposed wherein Li+ ion adsorption stabilizes TiO2 acceptor states resulting in energetically more favorable interfacial electron transfer. The photophysical and photoelectrochemical properties of porous nanocrystalline anatase TiO2 electrodes modified with Ru(deeb)(bpy)2 2+, Os(deeb)(bpy)22+, and mixtures of both are described in Chapters 4 and 5. In regenerative solar cells with 0.5 M LiI/0.05 M I2 acetonitrile electrolyte, both compounds efficiently inject electrons into TiO2 producing monochromatic incident photon-to-current efficiencies (IPCE), IPCE (460 nm) = 0.70 + 0

  12. Fabrication of nanostructured metal oxide films with supercritical carbon dioxide: Processing and applications

    NASA Astrophysics Data System (ADS)

    You, Eunyoung

    Nanostructured metal oxide films have many applications in catalysis, microelectronics, microfluidics, photovoltaics and other fields. Since the performance of a device depends greatly on the structure of the material, the development of methodologies that enable prescriptive control of morphology are of great interest. The focus of this work is to control the structure and properties of the nanostructured metal oxide films using novel synthetic schemes in supercritical fluids and to use those films as key building components in alternative energy applications. A supercritical fluid is a substance at a temperature and pressure above its critical point. It typically exhibits gas-like transport properties and liquid-like densities. Supercritical fluid deposition (SFD) utilizes these properties of supercritical CO2 (scCO2) to deposit chemically pure metal, oxides and alloys of metal films. SFD is a chemical vapor deposition (CVD)-like process in the sense that it uses similar metal organic precursors and deposits films at elevated temperatures. Instead of vaporizing or subliming the precursors, they are dissolved in supercritical fluids. SFD has typically shown to exhibit higher precursor concentrations, lower deposition temperatures, conformal deposition of films on high aspect ratio features as compared to CVD. In2 O3, ZnO and SnO2 are attractive materials because they are used in transparent conductors. SFD of these materials were studied and In2 O3 deposition kinetics using tris(2,2,6,6-tetramethyl-3,5-heptanedionato) In (III) as precursor were determined. Growth rate dependence on the deposition temperature and the precursor concentrations were studied and the physicochemical and optical properties of In2 O3 films were characterized. Metal oxide nanochannels that can potentially be used for microfluidics have been fabricated by sequentially performing nanoimprint lithography (NIL) and SFD. NIL was used to pattern photoresist grating on substrates and SFD of TiO2

  13. Theoretical study of the α +d →6Li +γ astrophysical capture process in a three-body model

    NASA Astrophysics Data System (ADS)

    Tursunov, E. M.; Kadyrov, A. S.; Turakulov, S. A.; Bray, I.

    2016-07-01

    The astrophysical capture process α +d →6Li is studied in a three-body model. The initial state is factorized into the deuteron bound state and the (α +d )-scattering state. The final nucleus 6Li (1+) is described as a three-body bound state α +n +p in the hyperspherical Lagrange-mesh method. The contribution of the E 1 -transition operator from the initial isosinglet states to the isotriplet components of the final state is estimated to be negligible. An estimation of the forbidden E 1 transition to the isosinglet components of the final state is comparable with the corresponding results of the two-body model. However, the contribution of the E 2 -transition operator is found to be much smaller than the corresponding estimations of the two-body model. The three-body model perfectly matches the new experimental data of the LUNA Collaboration with the spectroscopic factor of 2.586 estimated from the bound-state wave functions of 6Li and a deuteron.

  14. Shallow and deep earthquake sequences captured in the North Tanzanian Divergence, East Africa: Inferences on seismogenic processes and rheology

    NASA Astrophysics Data System (ADS)

    Albaric, J.; Perrot, J.; Déverchère, J.; Deschamps, A.; Ferdinand, R. W.; Le Gall, B.

    2009-12-01

    Using a temporary local seismic network of 35 stations deployed in North Tanzania (SEISMOTANZ'07 experiment) during 6 months in 2007, we captured two earthquake sequences (Gelai and Manyara) occurring respectively in the southern end of the Kenya rift and in the North Tanzanian Divergence (NTD). None of the sequences depicts typical swarm or mainshock-aftershock patterns. Although distant of only ~150 km, their triggering mechanisms appear to be different. They highlight a major change in the magmatic/tectonic nature of the rift where the eastern branch of the Est African Rift enters the Tanzanian craton. Both depict similar shape and long-axis, emphasizing the preferred locus of active strain release along NE-SW discontinuities which probably root at depth into steep Proterozoic shear zones. At Gelai, the deformation is dominated by aseismic processes involving slow slip on a normal fault and dyke intrusion within the upper crust, and an interaction with the eruption of the nearby Oldoinyo Lengai volcano. At Manyara, the sequence reveals a long-lasting seismic activity deeply rooted (~20-35 km depth), possibly indicative of stress loading transmitted laterally. Focal solutions demonstrate a mixture of normal and strike slip faulting on sub-vertical inherited structures striking N60°E. The yield stress envelope modelled from the depth frequency distribution of earthquakes in Manyara is consistent with the presence of a mafic lower crust and further supports the strength increase of the rifted crust from south Kenya to the NTD.

  15. Seam tracking with adaptive image capture for fine-tuning of a high power laser welding process

    NASA Astrophysics Data System (ADS)

    Lahdenoja, Olli; Säntti, Tero; Laiho, Mika; Paasio, Ari; Poikonen, Jonne K.

    2015-02-01

    This paper presents the development of methods for real-time fine-tuning of a high power laser welding process of thick steel by using a compact smart camera system. When performing welding in butt-joint configuration, the laser beam's location needs to be adjusted exactly according to the seam line in order to allow the injected energy to be absorbed uniformly into both steel sheets. In this paper, on-line extraction of seam parameters is targeted by taking advantage of a combination of dynamic image intensity compression, image segmentation with a focal-plane processor ASIC, and Hough transform on an associated FPGA. Additional filtering of Hough line candidates based on temporal windowing is further applied to reduce unrealistic frame-to-frame tracking variations. The proposed methods are implemented in Matlab by using image data captured with adaptive integration time. The simulations are performed in a hardware oriented way to allow real-time implementation of the algorithms on the smart camera system.

  16. Novel method of niosome generation using supercritical carbon dioxide part I: process mechanics.

    PubMed

    Wagner, Michael E; Rizvi, Syed S H

    2015-01-01

    A novel method for the production of non-ionic surfactant vesicles (niosomes) using an rapid expansion of supercritical solution (RESS)-based process coupled with a gas ejector is presented along with an investigation of parameters affecting niosome morphology, size and encapsulation efficiency of a 0.2 M D-glucose solution in Tris buffer at physiological pH. The solubility of the non-ionic surfactant polyoxyethylene(4) sorbitan monostearate in SC-CO2 was determined at three pressures (10, 15 and 20 MPa) and three temperatures (40, 50 and 60 °C). Mole fraction of Tween61 in the vapor phase increased with pressure at 40 °C, but did not change with pressure at 50 or 60 °C. Solubility data were correlated using the Peng-Robinson equation of state (PREOS) with the Panagiotopoulos and Reid mixing rule. Vesicles were either multilamellar or unilamellar, depending on the degree of precipitation of the lipid formulation at the point of aqueous cargo introduction. Vesicle particle size distributions were bimodal, with the 80-99% of the liposomal volume contributed niosomes ranging in size from 3 to 7 μm and the remaining niosomes ranging from 239 to 969 nm, depending on the system configuration. Encapsulation efficiency as high as 28% using the gas ejector to introduce the glucose cargo solution was achieved. Vesicle particle size and encapsulation efficiency were shown to be dependent on cargo droplet formation.

  17. The future of carbon dioxide for polymer processing in tissue engineering.

    PubMed

    Bhamidipati, Manjari; Scurto, Aaron M; Detamore, Michael S

    2013-06-01

    The use of CO2 for scaffold fabrication in tissue engineering was popularized in the mid-1990 s as a tool for producing polymeric foam scaffolds, but had fallen out of favor to some extent, in part due to challenges with pore interconnectivity. Pore interconnectivity issues have since been resolved by numerous dedicated studies that have collectively outlined how to control the appropriate parameters to achieve a pore structure desirable for tissue regeneration. In addition to CO2 foaming, several groups have leveraged CO2 as a swelling agent to impregnate scaffolds with drugs and other bioactive additives, and for encapsulation of plasmids within scaffolds for gene delivery. Moreover, in contrast to CO2 foaming, which typically relies on supercritical CO2 at very high pressures, CO2 at much lower pressures has also been used to sinter polymeric microspheres together in the presence of cells to create cell-seeded scaffolds in a single step. CO2 has a number of advantages for polymer processing in tissue engineering, including its ease of use, low cost, and the opportunity to circumvent the use of organic solvents. Building on these advantages, and especially now with the tremendous precedent that has paved the way in defining operating parameters, and making the technology accessible for new groups to adapt, we invite and encourage our colleagues in the field to leverage CO2 as a new tool to enhance their own respective unique capabilities.

  18. The Future of Carbon Dioxide for Polymer Processing in Tissue Engineering

    PubMed Central

    Bhamidipati, Manjari; Scurto, Aaron M.

    2013-01-01

    The use of CO2 for scaffold fabrication in tissue engineering was popularized in the mid-1990s as a tool for producing polymeric foam scaffolds, but had fallen out of favor to some extent, in part due to challenges with pore interconnectivity. Pore interconnectivity issues have since been resolved by numerous dedicated studies that have collectively outlined how to control the appropriate parameters to achieve a pore structure desirable for tissue regeneration. In addition to CO2 foaming, several groups have leveraged CO2 as a swelling agent to impregnate scaffolds with drugs and other bioactive additives, and for encapsulation of plasmids within scaffolds for gene delivery. Moreover, in contrast to CO2 foaming, which typically relies on supercritical CO2 at very high pressures, CO2 at much lower pressures has also been used to sinter polymeric microspheres together in the presence of cells to create cell-seeded scaffolds in a single step. CO2 has a number of advantages for polymer processing in tissue engineering, including its ease of use, low cost, and the opportunity to circumvent the use of organic solvents. Building on these advantages, and especially now with the tremendous precedent that has paved the way in defining operating parameters, and making the technology accessible for new groups to adapt, we invite and encourage our colleagues in the field to leverage CO2 as a new tool to enhance their own respective unique capabilities. PMID:23289736

  19. Bench-Scale Development of a Hybrid Membrane-Absorption CO{sub 2} Capture Process: Preliminary Cost Assessment

    SciTech Connect

    Freeman, Brice; Kniep, Jay; Pingjiao, Hao; Baker, Richard; Rochelle, Gary; Chen, Eric; Frailie, Peter; Ding, Junyuan; Zhang, Yue

    2014-03-31

    This report describes a study of capture costs for a hybrid membrane-absorption capture system based on Membrane Technology and Research, Inc. (MTR)’s low-pressure membrane contactors and the University of Texas at Austin’s 5 m piperazine (PZ) Advanced Flash Stripper (AFS; 5 m PZ AFS) based CO2 capture system. The report is submitted for NETL review, and may be superseded by a final topical report on this topic that will be submitted to satisfy the Task 2 report requirement of the current project (DE-FE0013118).

  20. Studies on process parameters for chlorine dioxide production using IrO2 anode in an un-divided electrochemical cell.

    PubMed

    Pillai, K Chandrasekara; Kwon, Tae Ouk; Park, Bo Bae; Moon, Il Shik

    2009-05-30

    Chlorine dioxide is potentially a powerful oxidant with environmentally compatible application in several strategic areas relating to pollution control typically for water disinfection, and its sustained production is a key factor for its successful application. Although increased attention has been paid for on-line chlorine dioxide generation by several chemical and electrochemical methods, the details are mostly confined as patents. We studied in this work the electrochemical generation of chlorine dioxide from an un-buffered solution of sodium chlorite and sodium chloride mixture in an un-divided electrochemical cell under constant current mode, with a view to optimize various process parameters, which have a direct bearing on the chlorine dioxide formation efficiency under laboratory conditions. The effect of feed flow rate (10-150 ml min(-1)), feed solution pH (2.3-5.0), concentration of sodium chloride (0-169.4mM), concentration of sodium chlorite (0-7.7 mM), and the applied current (100-1200 mA) on the formation of dissolved ClO(2) gas in solution and the pH of the product-containing solution was investigated by performing single pass experiments, with no circulation, in a cell set-up with Ti/IrO(2) anode and Ti/Pt cathode. The current efficiency and the power consumption were calculated for the optimized conditions. PMID:18838217

  1. A calcium oxide sorbent process for bulk separation of carbon dioxide

    SciTech Connect

    Harrison, D.P.

    1990-09-01

    This research effort is designed to investigate the technical feasibility of a high-temperature, high-pressure process for the bulk separation of CO{sub 2} from coal-derived gases. The two-year contract was awarded in September 1989. This report describes the research effort and results obtained during the first year of the effort. The overall project consists of 6 tasks, four of which were active during year 01. Tasks 1 and 2 were completed during the year while activity in Tasks 3 and 6 will carry over into year 02. Tasks 4 and 5 will be initiated during year 02. Three primary objectives were met in Task 1. A literature search on the calcination-carbonation reactions of CO{sub 2} with calcium-based sorbents was completed. A high temperature, high pressure (HTHP) electrobalance reactor suitable for studying the calcination and carbonation reactions was constructed. This reactor system is now fully operable and we are routinely collecting kinetics data at temperatures in the range of 550-900{degree}C and pressures of 1 to 15 atm. Samples of nine candidate calcium-based sorbents were acquired and tested. These samples were subjected to reaction screening tests as part of Task 2. As a result of these screening tests, chemically pure calcium carbonate, chemically pure calcium acetate, and the commercial dolomite were selected for more detailed kinetic testing. In Task 3, the HTHP electrobalance reactor is being used to study the calcination-carbonation behavior of the three base sorbents as a function of calcination temperature, carbonation temperature, carbonation pressure, and CO{sub 2} concentration.

  2. Economic and energetic analysis of capturing CO2 from ambient air

    PubMed Central

    House, Kurt Zenz; Baclig, Antonio C.; Ranjan, Manya; van Nierop, Ernst A.; Wilcox, Jennifer; Herzog, Howard J.

    2011-01-01

    Capturing carbon dioxide from the atmosphere (“air capture”) in an industrial process has been proposed as an option for stabilizing global CO2 concentrations. Published analyses suggest these air capture systems may cost a few hundred dollars per tonne of CO2, making it cost competitive with mainstream CO2 mitigation options like renewable energy, nuclear power, and carbon dioxide capture and storage from large CO2 emitting point sources. We investigate the thermodynamic efficiencies of commercial separation systems as well as trace gas removal systems to better understand and constrain the energy requirements and costs of these air capture systems. Our empirical analyses of operating commercial processes suggest that the energetic and financial costs of capturing CO2 from the air are likely to have been underestimated. Specifically, our analysis of existing gas separation systems suggests that, unless air capture significantly outperforms these systems, it is likely to require more than 400 kJ of work per mole of CO2, requiring it to be powered by CO2-neutral power sources in order to be CO2 negative. We estimate that total system costs of an air capture system will be on the order of $1,000 per tonne of CO2, based on experience with as-built large-scale trace gas removal systems. PMID:22143760

  3. Studies of solid carbon dioxide in interstellar ice analogs subject to thermal processing

    NASA Astrophysics Data System (ADS)

    White, Douglas W.

    2010-09-01

    determined from the TPD traces of these experiments. The work provided here addresses the physical properties of solid CO 2 thermally processed in ice mixtures in interstellar environments by laboratory simulations spectroscopically analyzed by mid-infrared absorption profiles and TPD.

  4. The Wood-Growth-and-Burial Process (WGBP) Permanent Wood Sequestration to Solve the Global Carbon Dioxide Problem

    NASA Astrophysics Data System (ADS)

    Scholz, F.; Hasse, U.

    2008-12-01

    , or/and via very slightly increased energy prices. It is a great advantage of the WGBP that it will not be competitive with the agriculture, as the areas most suitable for the process are not attractive for the growth of food or energy plants. The WGBP does not need fertilizers and irrigation, and it does not need genetically engineered plants. It is completely ecological and environmentally friendly. The WGBP can be performed at almost any place of the world, and it is not necessary to perform the process at the sites of carbon dioxide emission. The WGBP will contribute to a fair international trade. The WGBP will be equally available to all countries and societies of the world. There is no discrimination of poorer or less advanced societies. The WGBP will produce wood deposits for future generation, which once may become sources for biomass processing technologies, be it for the production of chemicals of energy. The burial sites will be saving banks of precious material. Ref.: F. Scholz, U. Hasse: ChemSusChem 1 (2008) 381-384 greifswald.de/~analytik/

  5. Bench-scale Development of an Advanced Solid Sorbent-based CO2 Capture Process for Coal-fired Power Plants

    SciTech Connect

    Nelson, Thomas; Kataria, Atish; Soukri, Mustapha; Farmer, Justin; Mobley, Paul; Tanthana, Jak; Wang, Dongxiang; Wang, Xiaoxing; Song, Chunshan

    2015-12-31

    It is increasingly clear that CO2 capture and sequestration (CCS) must play a critical role in curbing worldwide CO2 emissions to the atmosphere. Development of these technologies to cost-effectively remove CO2 from coal-fired power plants is very important to mitigating the impact these power plants have within the world’s power generation portfolio. Currently, conventional CO2 capture technologies, such as aqueous-monoethanolamine based solvent systems, are prohibitively expensive and if implemented could result in a 75 to 100% increase in the cost of electricity for consumers worldwide. Solid sorbent CO2 capture processes – such as RTI’s Advanced Solid Sorbent CO2, Capture Process – are promising alternatives to conventional, liquid solvents. Supported amine sorbents – of the nature RTI has developed – are particularly attractive due to their high CO2 loadings, low heat capacities, reduced corrosivity/volatility and the potential to reduce the regeneration energy needed to carry out CO2 capture. Previous work in this area has failed to adequately address various technology challenges such as sorbent stability and regenerability, sorbent scale-up, improved physical strength and attrition-resistance, proper heat management and temperature control, proper solids handling and circulation control, as well as the proper coupling of process engineering advancements that are tailored for a promising sorbent technology. The remaining challenges for these sorbent processes have provided the framework for the project team’s research and development and target for advancing the technology beyond lab- and bench-scale testing. Under a cooperative agreement with the US Department of Energy, and part of NETL’s CO2 Capture Program, RTI has led an effort to address and mitigate the challenges associated with solid sorbent CO2 capture. The overall objective

  6. A zirconium dioxide ammonia microsensor integrated with a readout circuit manufactured using the 0.18 μm CMOS process.

    PubMed

    Lin, Guan-Ming; Dai, Ching-Liang; Yang, Ming-Zhi

    2013-03-15

    The study presents an ammonia microsensor integrated with a readout circuit on-a-chip fabricated using the commercial 0.18 μm complementary metal oxide semiconductor (CMOS) process. The integrated sensor chip consists of a heater, an ammonia sensor and a readout circuit. The ammonia sensor is constructed by a sensitive film and the interdigitated electrodes. The sensitive film is zirconium dioxide that is coated on the interdigitated electrodes. The heater is used to provide a working temperature to the sensitive film. A post-process is employed to remove the sacrificial layer and to coat zirconium dioxide on the sensor. When the sensitive film adsorbs or desorbs ammonia gas, the sensor produces a change in resistance. The readout circuit converts the resistance variation of the sensor into the output voltage. The experiments show that the integrated ammonia sensor has a sensitivity of 4.1 mV/ppm.

  7. 5A Zirconium Dioxide Ammonia Microsensor Integrated with a Readout Circuit Manufactured Using the 0.18 μm CMOS Process

    PubMed Central

    Lin, Guan-Ming; Dai, Ching-Liang; Yang, Ming-Zhi

    2013-01-01

    The study presents an ammonia microsensor integrated with a readout circuit on-a-chip fabricated using the commercial 0.18 μm complementary metal oxide semiconductor (CMOS) process. The integrated sensor chip consists of a heater, an ammonia sensor and a readout circuit. The ammonia sensor is constructed by a sensitive film and the interdigitated electrodes. The sensitive film is zirconium dioxide that is coated on the interdigitated electrodes. The heater is used to provide a working temperature to the sensitive film. A post-process is employed to remove the sacrificial layer and to coat zirconium dioxide on the sensor. When the sensitive film adsorbs or desorbs ammonia gas, the sensor produces a change in resistance. The readout circuit converts the resistance variation of the sensor into the output voltage. The experiments show that the integrated ammonia sensor has a sensitivity of 4.1 mV/ppm. PMID:23503294

  8. A study of alternative methods for reclaiming oxygen from carbon dioxide and water by a solid-electrolyte process for spacecraft applications

    NASA Technical Reports Server (NTRS)

    1971-01-01

    Two alternative technical approaches were studied for application of an electrochemical process using a solid oxide electrolyte (zirconia stabilized by yttria or scandia) to oxygen reclamation from carbon dioxide and water, for spacecraft life support systems. Among the topics considered are the advisability of proceeding to engineering prototype development and fabrication of a full scale model for the system concept, the optimum choice of method or approach to be carried into prototype development, and the technical problem areas which exist.

  9. Efficiency enhancement for natural gas liquefaction with CO2 capture and sequestration through cycles innovation and process optimization

    NASA Astrophysics Data System (ADS)

    Alabdulkarem, Abdullah

    Liquefied natural gas (LNG) plants are energy intensive. As a result, the power plants operating these LNG plants emit high amounts of CO2 . To mitigate global warming that is caused by the increase in atmospheric CO2, CO2 capture and sequestration (CCS) using amine absorption is proposed. However, the major challenge of implementing this CCS system is the associated power requirement, increasing power consumption by about 15--25%. Therefore, the main scope of this work is to tackle this challenge by minimizing CCS power consumption as well as that of the entire LNG plant though system integration and rigorous optimization. The power consumption of the LNG plant was reduced through improving the process of liquefaction itself. In this work, a genetic algorithm (GA) was used to optimize a propane pre-cooled mixed-refrigerant (C3-MR) LNG plant modeled using HYSYS software. An optimization platform coupling Matlab with HYSYS was developed. New refrigerant mixtures were found, with savings in power consumption as high as 13%. LNG plants optimization with variable natural gas feed compositions was addressed and the solution was proposed through applying robust optimization techniques, resulting in a robust refrigerant which can liquefy a range of natural gas feeds. The second approach for reducing the power consumption is through process integration and waste heat utilization in the integrated CCS system. Four waste heat sources and six potential uses were uncovered and evaluated using HYSYS software. The developed models were verified against experimental data from the literature with good agreement. Net available power enhancement in one of the proposed CCS configuration is 16% more than the conventional CCS configuration. To reduce the CO2 pressurization power into a well for enhanced oil recovery (EOR) applications, five CO2 pressurization methods were explored. New CO2 liquefaction cycles were developed and modeled using HYSYS software. One of the developed

  10. [Evaluation of potentiality of combined SHF- and glow discharge in intensification of carbon dioxide and hydrogen processing within life support system].

    PubMed

    Klimarev, S I

    2011-01-01

    The article reports an experimental carbon dioxide hydration process in combined SHF- and glow discharge, and describes a design of SHF plasmatrones for CO2 processing at air pressure and in an integrated unit. Maximal transformation of 80% CO2 per a run was reached with the total input power of no more than 0.9 kW. Thermal zero lag of plasma forming, essentially instant and timely engagement and disengagement of thermal action on CO2-H2 mixture renders SHF-energy applicable to intensification of next generation life support technologies, processing of these gases within atmosphere regeneration system specifically.

  11. Palladium-catalyzed synthesis of ammonium sulfinates from aryl halides and a sulfur dioxide surrogate: a gas- and reductant-free process.

    PubMed

    Emmett, Edward J; Hayter, Barry R; Willis, Michael C

    2014-09-15

    Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and despite a variety of preparative methods being available, processes which introduce the most basic sulfonyl building block, sulfur dioxide, using catalytic methods, are rare. Described herein is a simple reaction system consisting of the sulfur dioxide surrogate DABSO, triethylamine, and a palladium(0) catalyst for effective convertion of a broad range of aryl and heteroaryl halides into the corresponding ammonium sulfinates. Key features of this gas- and reductant-free reaction include the low loadings of palladium (1 mol%) and ligand (1.5 mol%) which can be employed, and the use of isopropyl alcohol as both a solvent and formal reductant. The ammonium sulfinate products are converted in situ into a variety of sulfonyl-containing functional groups, including sulfones, sulfonyl chlorides, and sulfonamides.

  12. Thermal Integration of CO{sub 2} Compression Processes with Coal-Fired Power Plants Equipped with Carbon Capture

    SciTech Connect

    Edward Levy

    2012-06-29

    Coal-fired power plants, equipped either with oxycombustion or post-combustion CO{sub 2} capture, will require a CO{sub 2} compression system to increase the pressure of the CO{sub 2} to the level needed for sequestration. Most analyses show that CO{sub 2} compression will have a significant effect on parasitic load, will be a major capital cost, and will contribute significantly to reduced unit efficiency. This project used first principle engineering analyses and computer simulations to determine the effects of utilizing compressor waste heat to improve power plant efficiency and increase net power output of coal-fired power plants with carbon capture. This was done for units with post combustion solvent-based CO{sub 2} capture systems and for oxyfired power plants, firing bituminous, PRB and lignite coals. The thermal integration opportunities analyzed for oxycombustion capture are use of compressor waste heat to reheat recirculated flue gas, preheat boiler feedwater and predry high-moisture coals prior to pulverizing the coal. Among the thermal integration opportunities analyzed for post combustion capture systems are use of compressor waste heat and heat recovered from the stripper condenser to regenerate post-combustion CO{sub 2} capture solvent, preheat boiler feedwater and predry high-moisture coals. The overall conclusion from the oxyfuel simulations is that thermal integration of compressor heat has the potential to improve net unit heat rate by up to 8.4 percent, but the actual magnitude of the improvement will depend on the type of heat sink used and to a lesser extent, compressor design and coal rank. The simulations of a unit with a MEA post combustion capture system showed that thermal integration of either compressor heat or stripper condenser heat to preheat boiler feedwater would result in heat rate improvements from 1.20 percent to 4.19 percent. The MEA capture simulations further showed that partial drying of low rank coals, done in combination

  13. Research Electronic Data Capture (REDCap) - A metadata-driven methodology and workflow process for providing translational research informatics support

    PubMed Central

    Harris, Paul A.; Taylor, Robert; Thielke, Robert; Payne, Jonathon; Gonzalez, Nathaniel; Conde, Jose G.

    2009-01-01

    REDCap is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: 1) a brief description of the REDCap metadata-driven software toolset; 2) detail concerning the capture and use of study-related metadata from scientific research teams; 3) measures of impact for REDCap; 4) details concerning a consortium network of domestic and international institutions collaborating on the project; and 5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions. PMID:18929686

  14. Simple Host−Guest Chemistry To Modulate the Process of Concentration and Crystallization of Membrane Proteins by Detergent Capture in a Microfluidic Device

    SciTech Connect

    Li, Liang; Nachtergaele, Sigrid; Seddon, Annela M.; Tereshko, Valentina; Ponomarenko, Nina; Ismagilov, Rustem F.

    2009-01-15

    This paper utilizes cyclodextrin-based host-guest chemistry in a microfluidic device to modulate the crystallization of membrane proteins and the process of concentration of membrane protein samples. Methyl-{beta}-cyclodextrin (MBCD) can efficiently capture a wide variety of detergents commonly used for the stabilization of membrane proteins by sequestering detergent monomers. Reaction Center (RC) from Blastochloris viridis was used here as a model system. In the process of concentrating membrane protein samples, MBCD was shown to break up free detergent micelles and prevent them from being concentrated. The addition of an optimal amount of MBCD to the RC sample captured loosely bound detergent from the protein-detergent complex and improved sample homogeneity, as characterized by dynamic light scattering. Using plug-based microfluidics, RC crystals were grown in the presence of MBCD, giving a different morphology and space group than crystals grown without MBCD. The crystal structure of RC crystallized in the presence of MBCD was consistent with the changes in packing and crystal contacts hypothesized for removal of loosely bound detergent. The incorporation of MBCD into a plug-based microfluidic crystallization method allows efficient use of limited membrane protein sample by reducing the amount of protein required and combining sparse matrix screening and optimization in one experiment. The use of MBCD for detergent capture can be expanded to develop cyclodextrin-derived molecules for fine-tuned detergent capture and thus modulate membrane protein crystallization in an even more controllable way.

  15. Multitemporal 3D data capturing and GIS analysis of fluvial processes and geomorphological changes with terrestrial laser scanning

    NASA Astrophysics Data System (ADS)

    Hämmerle, Martin; Forbriger, Markus; Höfle, Bernhard

    2013-04-01

    LiDAR is a state of the art method for directly capturing 3D geodata. A laser beam is emitted in a known direction. The time of flight of the laser pulse is recorded and transformed into the distance between sensor and scanned object. The result of the scanning process is a 3D laser point cloud densely covering the surveyed area. LiDAR is used in a vast variety of research fields. In this study, the focus is on the application of terrestrial laser scanning (TLS), the static and ground-based LiDAR operation, in a multitemporal analysis of fluvial geomorphology. Within the framework of two study projects in 2011/2012, two TLS surveys were carried out. The surveys covered a gravel bar of about 150 m × 25 m size in a side branch of the Neckar River near Heidelberg (49°28'36''N, 8°34'32''E) located in a nature reserve with natural river characteristics. The first survey was performed in November 2011, the second in June 2012. Due to seasonally changing water levels, the gravel bar was flooded and the morphology changed. For the field campaigns, a Riegl VZ-400 was available. Height control points and tie points for registration and georeferencing were obtained with a total station and GPS equipment. The first survey was done from 6 scan positions (77 million points) and the second from 5 positions (89 million points). The point spacing for each single scan was set to 3 mm at 10 m distance. Co-registration of the individual campaigns was done via an Iterative Closest Point algorithm. Thereafter, co-registration and fine georeferencing of both epochs was performed using manually selected tie points and least-squares adjustment. After filtering of vegetation in the 3D point cloud in the software OPALS, a digital terrain model (DTM) with 0.25 m by 0.25 m cell size was generated for each epoch. A difference raster model of the two DTMs for assessing the changes was derived excluding water surface areas using the signal amplitude recorded for each echo. From the mean

  16. Annual Report: Carbon Capture (30 September 2012)

    SciTech Connect

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

    2014-04-16

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

  17. Improving outpatient charge capture.

    PubMed

    Gautschi, Daniel; Sanderson, Brian

    2014-10-01

    Hospitals can identify opportunities to enhance revenue collection by closely analyzing outpatient charge-capture data. A hospital can bolster its charge-capture analysis by performing a charge-capture process walk-through and scrutinizing subsystem links, third-party payer contracts, and electronic health record structures. The hospital then can integrate charge-integrity functions into clinical departments as needed by developing charge-reconciliation tools and reports and monitoring their utilization, and incorporating charge-reconciliation responsibilities into clinical department managers' job descriptions and goals. PMID:25647902

  18. Thermal neutron capture cross-section to 113Cd isomer for the study of s-process origin of 115Sn

    NASA Astrophysics Data System (ADS)

    Hayakawa, Takehito; Shizuma, Toshiyuki; Chiba, Satoshi; Kajino, Toshitaka; Hatsukawa, Yuichi; Iwamoto, Nobuyuki; Shinohara, Nobuo; Harada, Hideo

    2010-06-01

    The astrophysical origin of a p-nucleus 115Sn has remained still an open question. The nucleus 115Sn may be produced by a weak branch of the s-process through a β-unstable isomer in 113Cd. However, a neutron capture cross-section to this isomer has not been measured with high accuracy at any energy. A neutron capture cross-section for the 112Cd(n,γ)113Cdm reaction has been measured with neutrons provided from a nuclear reactor. The nucleus 115Sn may be produced by a nucleosynthesis flow through 113Cdm in the s-process. We have obtained the thermal neutron capture cross-section of 0.028+/-0.009 [b] and the resonance integral of 1.1+/-0.3 [b] using a cadmium difference method. The cross-section ratio of the isomer to the ground state has been calculated as a function of the incident neutron energy, E, by using a statistical model. The calculated ratios are almost constant over a wide range of E<100 keV. We have evaluated the s-process contribution to the solar abundance of 115Sn using the classical steady-flow model. This calculated result has shown that the production through 113Cdm may be minor contribution to 115Sn.

  19. Capturing Movement

    ERIC Educational Resources Information Center

    Lord, Lynda

    2007-01-01

    The idea for the art lesson presented in this article grew out of watching the lively actions of fourth grade students. Since drawing is the author's first love, she is always looking for new ways to teach it. This time, instead of setting up a still life, she decided to teach students how to capture their actions on paper. (Contains 5 online…

  20. High-Resolution Neutron Capture and Total Cross-Section Measurements, and the Astrophysical 95Mo(n,gamma) Reaction Rate at s-process Temperatures

    SciTech Connect

    Koehler, Paul Edward; Guber, Klaus H; Harvey, John A; Wiarda, Dorothea

    2008-01-01

    Abundances of Mo isotopes predicted by stellar models of the s process are, except for {sup 95}Mo, in good agreement with data from single grains of mainstream presolar SiC. Because the meteorite data seemed sound and no reasonable modification to stellar theory resulted in good agreement for {sup 95}Mo, it has been suggested that the recommended neutron capture reaction rate for this nuclide is 30% too low. Therefore, we have made a new determination of the {sup 95}Mo(n,{gamma}) reaction rate via high-resolution measurements of the neutron-capture and total cross sections of {sup 95}Mo at the Oak Ridge Electron Linear Accelerator. These data were analyzed with the R-matrix code SAMMY to obtain parameters for resonances up to E{sub n} = 10 keV. Also, a small change to our capture apparatus allowed us to employ a new technique to vastly improve resonance spin and parity assignments. These new resonance parameters, together with our data in the unresolved range, were used to calculate the {sup 95}Mo(n,{gamma}) reaction rate at s-process temperatures. We compare the currently recommended rate to our new results and discuss their astrophysical impact.